Identification of Substituted Amino Acid Hydrazides as Novel Anti-Tubercular Agents, Using a Scaffold Hopping Approach

Abstract

Discovery and development of new therapeutic options for the treatment of Mycobacterium tuberculosis (Mtb) infection, particularly drug-resistant strains, are urgently required to tackle the global burden of this disease. Herein, we reported the synthesis of a novel series of N-substituted amino acid hydrazides, utilising a scaffold hopping approach within a library of anti-tubercular agents. Efficacy and selectivity were evaluated against three strains of Mtb (wild-type, isoniazid-resistant and rifampicin-resistant), and cytotoxicity against macrophages in vitro. The antibacterial activity and therapeutic index of these molecules were significantly affected by modifications with the N-substituents. Introduction of a 3,5-dinitroaryl moiety demonstrated enhanced antibacterial activity against all three strains of Mtb. In contrast, the inclusion of an imidazo [1,2-a]pyridine-3-carboxy moiety resulted in enhanced activity towards isoniazid mono-resistant Mtb relative to wild-type Mtb. Consequently, this scaffold hopping approach showed significant promise for exemplification of novel molecules with specific activity profiles against drug-resistant tuberculosis.

1. Introduction

The World Health OrganisatioN′s (WHO) global tuberculosis report in 2019 recognises tuberculosis (TB) as a communicable disease responsible for a major cause of long term illness and continues to be one of the top ten causes of death worldwide from a single infectious agent [1]. In 2018, an estimated ten million (range 9.0–11.1 million) new cases of TB infection were reported, equivalent to 132 cases per 100,000 population globally [2]. Unfortunately, treatment responses to TB are stagnating, and most WHO regions are now likely to fail to reach the 2020 milestone of the WHO′s End TB strategy [2]. Concerningly, there is an ever-increasing number of infections from strains resistant to the front line anti-TB drugs—rifampicin (RIF) and isoniazid (INH), exacerbating further the global TB epidemic [1]. Consequently, new drug molecules with novel modes of action are urgently required to address this increased disease burden and diminishing response to current therapies.

Over the past ten years, notable advances towards the development of new therapies against TB have been made. For instance, the dihydro-nitroimidazooxazole derivative—Delamanid (Deltyba^®®)—acts as a prodrug activated by the mycobacterial deazaflavin-dependent nitroreductase to an inhibitor of methoxy mycolic acid and ketomycolic acid synthesis of the mycobacterial cell wall [3]. Another such drug, dinitrobenzamide (DNB-1) has shown a novel mechanism involving inhibition of decaprenylphosphoryl-β-d-ribose 2′-epimerase (DprE1), a vital enzyme in cell wall lipoarabinomannan and arabinogalactan precursor biosynthesis [4]. Conversely, pyrazinamide, a clinically utilised drug since 1952 demonstrates activity against dormant or semi-dormant TB, with a mode of action involving multiple cellular targets focusing on the disruption of energy production and fatty acid synthesis [5]. However, despite the significant promise, resistance to several of these molecules has now been reported [5,6,7,8,9].

A notable new direction for the development of anti-TB drugs has been the perturbation of the mycobacterial respiratory electron transport chain (ETC), with several such drugs entering the clinic recently (Figure 1) [10]. The diarylquinoline Bedaquiline (SIRTURO^®®), used predominantly against drug-resistant TB, targets the mycobacterial respiratory chain enzyme F1/F0-ATPase [11,12]. Whereas the 1,2-ethylene diamine SQ109, shown to be active against both drug-sensitive and drug-resistant TB, has a mechanism involving inhibition of the Mycobacterial membrane protein Large 3 (MmpL3)-dependent export of mycolic acids but has also been linked to the dissipation of the proton motive force within the ETC [13]. More recently, the first in class drug—Q203 (Telacebec^®®), has shown a novel mechanism of action targeting the cytochrome bc1 complex of the ETC and has demonstrated significant promise in the clinic [14]. Furthermore, the therapeutic mechanism of the ‘old′ drug clofazimine, which has been repurposed for treatment of drug-resistant TB, also inhibits the NADH dehydrogenase (NAD-2) within the ETC [15]. Consequently, in order to tackle the problematic exacerbation of drug-resistant TB, the identification of drug targets outside of the conventional pathways for current drugs and subsequent discovery of drug molecules exploiting these new therapeutic avenues are required.

Our previous studies of benzoxa-[2,1,3]-diazole-substituted amino acid hydrazides demonstrated therapeutic selectivity of these molecules against mycolata over Gram-positive and Gram-negative bacteria [16]. This highlighted the involvement of the benzoxa-[2,1,3]-diazole, the amino acid (R₂) moiety and the substituted aryl hydrazine (R₁) towards bacterial selectivity, efficacy and establishment of a therapeutic index for development as a drug [16]. In this study, we evaluated variation of the benzoxa-[2,1,3]-diazole moiety within these compounds via the introduction of new architectures and their structure-activity-relationships toward the development of efficacious drugs against drug-resistant Mtb (Figure 2).

Strategy

Previously, we established the importance of the amino acid and hydrazide moieties within benzoxa-[2,1,3]-diazole-substituted amino acid hydrazides for selective therapeutic activity against Mtb [16]. The current study expanded upon this previous work and evaluated the impact of specific alteration of the benzoxa-[2,1,3]-diazole moiety towards the development of therapeutics with improved anti-Mtb activity, particularly towards drug-resistant Mtb. To achieve this objective, we adopted the scaffold hopping approach of known pharmacophores to identify putative molecules [17,18,19]. This predominantly focused on the utilisation of pharmacophores with known anti-Mtb activity amenable to incorporation at the site of the current benzoxa-[2,1,3]-diazole moiety. We specifically evaluated pharmacophores from drugs targeting the mycobacterial cell wall, isoniazid (INH) 1 and the 3,5-dinitrobenzene moiety of DNB-1, 2; the multi-target drug Pyrazinamide 3; the new generation of molecules perturbing the mycobacterial ETC, the quinoline and naphthalene of Bedaquiline 4 and the imidazo [1,2-a]pyridine-3-carboxy moiety of Q203 5 (Figure 3).

Both the amino acid and hydrazide moieties were locked within the structure, utilising 4-trifluoromethylphenyl 6–7 and 3-chlorophenyl hydrazine 8–9. In terms of the amino acids, we previously demonstrated alanine (Ala) to exhibit the highest activity when conjugated within these hydrazides [16]. To recapitulate the sulphur moiety present within several known anti-TB drugs [20], amino acids with this functionality were previously evaluated within the hydrazides. As cysteine was nucleophilic and not amenable to the introduction, methionine (Met) was utilised. Linkage of Met to either the 4-trifluoromethylphenyl or the 3-chlorophenyl hydrazine produced comparable therapeutic activity against Mtb and a therapeutic index similar to that of 6, containing Ala. The choice of hydrazides was based on the fact that 4-trifluoromethylphenyl hydrazide 6 had exhibited moderate activity against Mtb and a significant therapeutic index relative to cytotoxicity against mammalian cells, and 3-chlorophenyl hydrazine 8 had demonstrated notable impact upon Mtb therapeutic activity [16].

The objective of this study was to evaluate the importance of modifying the benzoxa-[2,1,3]-diazole moiety scaffold with those from other molecules with known anti-TB activity in order to appraise the therapeutic impact of substituents at this position and the potential for exploitation towards the development of molecules with demonstrated activity against drug-resistant Mtb.

2. Results and Discussion

2.1. Chemical Synthesis of Substituted Amino Acid Hydrazides

Previously established methods were employed to synthesise the substituted amino acid hydrazides starting from N-Boc amino acids and the corresponding hydrazide (Scheme 1).

Coupling of the mono-substituted hydrazine with the N-Boc amino acids was achieved, utilising standard peptide coupling reagents, in high yields to provide sufficient material to then allow coupling with the corresponding aryl carboxylic acids via the same procedure.

2.2. Structure-Activity Relationship of Therapeutic Activity against Mtb

Following the synthetic approach, the substituted amino acid hydrazides 6–37 were screened against drug-susceptible, INH or RIF mono-resistant strains of Mtb in a standard resazurin microtitre assay (REMA) [16,21]. Considering the entire results, all of the compounds broadly inhibited the growth of drug-susceptible and the mono-drug-resistant Mtb strains. In comparison with our previous studies using benzoxa-[2,1,3]-diazoles, we observed a level of antibacterial activity in the wild-type strain similar to or better than our lead compounds (Figure S1, Supporting Information). Notably, there was a greater antibacterial activity observed within the INH mono-resistant strain, implicating scope with this approach for the development of drugs with activity against drug-resistant Mtb.

No discernible difference in antibacterial activity with Boc-protected compounds was observed between the 4-trifluoromethylphenyl alanine (Ala) hydrazide 6 or 4-trifluoromethylphenyl methionine (Met) hydrazide 7. However, encouragingly, the Boc-protected 3-chlorophenyl Ala and 3-chlorophenyl Met hydrazide 8 and 9 demonstrated an observable increase in activity relative to the 4-trifluorophenyl amino acid hydrazides 6–7 (

Table 1. Results of synthesis of substituted amino acid hydrazides and the antibacterial activity and cytotoxicity.

				MIC (μM)
				Mtb			Mbv BCG		Mammalian Cell Toxicity
R	R1	R2	Compound	WT	Rif R	INH R	+pan	-pan
	4-CF3	CH3	6	46	92	92	-	-	13%
		(CH2)2SCH3	7	79	79	78	157	157	>80%
	3-Cl	CH3	8	51	13	3	204	204	<10%
		(CH2)2SCH3	9	22	21	3	171	171	<5%
	4-CF3	CH3	10	182	182	182	-	-	<5%
		(CH2)2SCH3	11	155	155	155	155	155	66%
	3-Cl	CH3	12	201	201	25	201	201	<5%
		(CH2)2SCH3	13	84	84	21	169	169	15%
	4-CF3	CH3	14	-	-	-	-	-	0%
		(CH2)2SCH3	15	155	155	155	-	-	55%
	3-Cl	CH3	16	50	50	6	50	50	25%
		(CH2)2SCH3	17	84	42	11	84	168	60%
	4-CF3	CH3	18	80	80	40	80	80	59%
		(CH2)2SCH3	19	35	35	35	69	69	>90%
	3-Cl	CH3	20	87	87	22	44	44	33%
		(CH2)2SCH3	21	-	-	19	-	-	60%
	4-CF3	CH3	22	80	80	80	159	80	15%
		(CH2)2SCH3	23	69	69	69	69	69	40%
	3-Cl	CH3	24	-	-	44	-	-	<5%
		(CH2)2SCH3	25	75	37	19	-	-	43%
	4-CF3	CH3	26	80	80	80	-	159	30%
		(CH2)2SCH3	27	138	35	69	138	138	>90%
	3-Cl	CH3	28	-	-	87	-	-	70%
		(CH2)2SCH3	29	37	37	9	75	75	60%
	4-CF3	CH3	30	36	36	36	18	18	>90%
		(CH2)2SCH3	31	8	4	8	16	16	>90%
	3-Cl	CH3	32	78	78	20	39	39	75%
		(CH2)2SCH3	33	34	9	17	34	34	>90%
	4-CF3	CH3	34	35	35	35	35	35	67%
		(CH2)2SCH3	35	-	-	62	-	-	>90%
	3-Cl	CH3	36	76	76	9	76	76	78%
		(CH2)2SCH3	37	33	33	8	33	33	>90%
			Isoniazid	0.2	0.07	-	0.4	0.4
			Rifampicin	0.02	-	0.02	0.02	0.02
			Ethambutol	4	4	4	20	20
			Ethionamide	6	6	6	12	12
			Erythromycin	0.2	0.17	0.17	0.09	0.09
			Kanamycin	-	-	-	-	-

WT = Wild type Mtb strain; Rif ^R = Rifampicin resistant Mtb strain; INH ^R = Isoniazid resistant Mtb strain; +pan = Pantothenate present in growth media; -pan = Pantothenate not present in growth media; - = Not active at the maximum assay concentration (64 μg/mL).

).

Substitution of the Boc with aryl heterocycles that mimic INH and pyrazinamide, 10–17, in most cases, did not provide enhanced antibacterial activity (Table 1). Albeit this substitution in one case actually afforded no therapeutic activity 14. However, differential selectivity was noted, with excellent activity against INH-resistant Mtb exhibited with the 3-chlorophenyl Ala and Met hydrazide of pyridine 12–13 and pyrazine 16–17 (Table 1). This notable observation is promising towards the development of therapies for drug-resistant Mtb, with significant potential that these compounds may employ a novel mechanism of action involving the circumventing of INH-activating enzyme, KatG, as the INH-resistant Mtb strain used in this study harboured an inactivating (Ser315 → Asp) in this protein, which was generated and identified in this study, analogous to previously published laboratory-generated and clinical strains [22].

An important criterion for any putative anti-TB drug is a demonstration of a clear therapeutic index between the concentration required to induce antibacterial activity and that which induces toxicity against the host system (i.e., macrophages and human tissueS). In this context, we set an arbitrary index of at least a 10-fold differential between the two outcomes. In the context of wild-type Mtb and RIF-resistant Mtb, none of the molecules demonstrated any discernible differential between antibacterial activity and mammalian cell cytotoxicity. Interestingly and in contrast, several molecules demonstrated a >10-fold therapeutic index when evaluated against INH-resistant Mtb. The Boc-protected 3-chlorophenyl Ala and Met hydrazides 8 and 9 gave excellent profiles, with a minimum inhibitory concentration (MIC) against INH-resistant Mtb of approximately 3 µM and less than 10% toxicity against macrophages at 100 µM, indicating a 30–40-fold therapeutic index. Although the pyrazine 3-chlorophenyl Ala and Met hydrazides 16 and 17 also exhibited selectivity toward INH-resistant Mtb, they demonstrated significant cytotoxicity against macrophages, implicating detrimental effects of the pyrimidine scaffold upon mammalian cells. The reasons for this are currently unclear.

The exploitation of the bedaquiline scaffolds, utilising the naphthalene and quinoline moieties (substituted at the 1-, 2- or 3- position with a carboxy group) 18–29, was evaluated as a strategy. Relative to the mono-substituted aryl heterocycles, this scaffold did not produce improved activity suggestive of further evaluation. Incorporation of the 2-substituted naphthalene moiety 18–21 produced a somewhat moderate, yet still disappointing, enhancement in anti-TB activity over 1- substituted naphthalene 22–25. Correspondingly, 3-substituted quinoline derivatives 26–29 displayed similar activity to the 2-naphthalene derivatives 18–21 with only the 4-trifluoromethylphenyl Met hydrazide 19 and 3-chlorophenyl Ala hydrazide 29 exhibiting anti-TB activity less than 50 µM. In support of these findings, a similar series of N-(alkoxyphenyl)-2-hydroxynaphthalene-1-carboxamides and their positional isomers N-(alkoxyphenyl)-1-hydroxynaphthalene-2-carboxamides have presented varied in vitro anti-TB activity (representative 12 μM and 97 μM, respectively) [23]. Further to demonstrating the poor antibacterial activity, the inclusion of the bedaquiline scaffold also proved to be detrimental to mammalian cells, supporting the cessation of this scaffold as an approach. The only notable outcome from this series was the putative selectivity of 3-chlorophenyl Ala hydrazide 29 against INH-resistant Mtb, with a MIC of 9 µM versus 37 µM against wild-type and RIF-resistant Mtb strains, albeit toxic against mammalian cells. This putative selectivity might be a consequence of bedaquiline inhibiting mycobacterial ATP synthase and counteracting the perturbation of the mycobacterial electron transport chain afforded by resistance to INH, as implicated in a recent study [24]. Further evaluation of this concept is, therefore, warranted.

Incorporation of 3,5-dinitrophenyl 30–33 resulted in viable antibacterial activity, with MIC values often <50 µM across all strains of Mtb. Interestingly, differential selectivity towards drug-resistant strains was observed within this series. The 3-chlorophenyl Ala hydrazide of 3,5-dinitrophenyl 32 showed similar activity against wild-type and RIF-resistant Mtb, with a 4-fold greater activity against INH-resistant Mtb. However, the 3-chlorophenyl Met hydrazide of 3,5-dinitrophenyl 33 showed increased activity relative to the Ala hydrazide against wild-type Mtb and a two-fold selectivity toward INH-resistant Mtb but surprisingly showed much greater activity against RIF-resistant Mtb with 4-fold selectivity over that of wild-type Mtb. This was the only compound in this series, demonstrating differential activity against RIF-resistant compared to wild-type Mtb, the mechanism of which is as yet unexplored but worthy of further investigations. Mechanistically, it is highly likely that these compounds 30–33 induce a general nitric oxide stress response similar to that observed with the known anti-TB compounds—metronidazole, delamanid and pretomanid—involving metabolic activation by enzymes, such as deazaflavin-dependent nitroreductase or the pyruvate-ferredoxin oxidereductase system, based on the fact they include nitro containing groups and functionality [25,26]. Such a mode of action involving oxidative stress would explain the fact that this series was highly toxic against mammalian cells. However, unlike metronidazole, delamanid and pretomanid, the activation mechanism must involve an enzymatic pathway common to both bacteria and mammalian cells.

The Q203 analogues 34–37 were of particular interest with respect to the development of molecules, exploiting new therapeutic pathways and bypassing conventional drug resistance mechanisms, for the treatment of drug-resistant Mtb. The imidazo[1,2-a]pyridine-3-carboxy moiety has been identified as the active component of several novel anti-tubercular drugs, including the pantothenate synthetase inhibitor GSK358607A and Q203 1, which targets the cytochrome bcc-aa3 supercomplex [27,28,29]. Although the 4-trifluoromethylphenyl imidazo[1,2-a]pyridine-3-carboxy-substituted hydrazides 34–35 demonstrated marginally better activity than their 3-chlorophenyl counterparts 36–37, no selectivity against drug-resistant strains of Mtb was observed with these compounds. With the 3-chlorophenyl imidazo[1,2-a]pyridine-3-carboxy-substituted hydrazides 36–37, the inclusion of Met over Ala resulted in a two-fold increase in antibacterial activity. In contrast to the 4-trifluoromethylphenyl-substituted hydrazides, the 3-chlorophenyl-substituted hydrazides showed exquisite selectivity toward INH-resistant Mtb with MIC values <10 µM for both the Ala 36 and Met 37 containing compounds. However, although showing potent antibacterial activity, all of the imidazo[1,2-a]pyridine-3-carboxy-substituted hydrazides exhibited significant toxicity against macrophages, implying their limited utility as viable drug molecules. Despite this, a greater understanding of the structure-activity relationship (SAR) and identification of the targets of these compounds is an important concept in improving our understanding of principles associated with their selectivity towards drug-resistant Mtb.

With respect to the imidazo[1,2-a]pyridine-3-carboxy-derived hydrazides 34–37, it was conceivable that the target of these compounds could include either the cytochrome supercomplex of proteins, as is the case with Q203 1, or pantothenate synthetase, the reported target of GSK358607A. Nevertheless, our results implied that the target was unlikely to be pantothenate synthetase since the Mtb mc²7000 strains used in this study possessed ΔpanCD gene deletions and relied on media supplementation with pantothenate for survival and growth, thereby abrogating dependency for growth upon this enzyme. Inclusion of the imidazo[1,2-a]pyridine-3-carboxy moiety resulted in equivalent or greater activity than the initial Boc-protected compounds 6–9. To further confirm this hypothesis, the activity of compounds 34–37 was evaluated against Mycobacterium bovis BCG as this constitutively expressed the pantothenate pathway. No difference in activity was detected with these compounds when in the presence or absence of pantothenate in the growth media with this mycobacterium, reinforcing pantothenate synthetase as unlikely to be the therapeutic target for these compounds. Furthermore, this target would also not explain the selectivity of these compounds for INH-resistant Mtb.

A more likely mechanism and one which provides a rationale for the increased selectivity of the 3-chlorophenyl imidazo[1,2-a]pyridine-3-carboxy-substituted hydrazides 36–37 towards INH-resistant Mtb is one analogous to that of Q203. This drug targets the cytochrome bcc-aa3 supercomplex and disrupts the ETC in mycobacteria [30]. Recently, in addition to inhibiting mycolic acid synthesis, the bactericidal activity of INH has also been linked to ATP production, increased oxygen consumption and subsequently perturbation of the mycobacterial ETC [24]. In this context, defects in NADH dehydrogenase and concomitantly ETC have been shown to confer resistance to INH in mycobacteria [31]. Further studies are thereby warranted to evaluate the involvement of this pathway in terms of conferring therapeutic selectivity of 3-chlorophenyl imidazo[1,2-a]pyridine-3-carboxy-substituted hydrazides towards INH-resistant Mtb. In addition, SAR studies to address the selectivity of the 3-chlorophenyl- but not the 4-trifluoromethylphenyl-substituted hydrazides are also important.

3. Materials and Methods

All reactions were carried out under a nitrogen atmosphere in glassware dried in the oven overnight (>75 °C) or under high vacuum by a heat-gun unless otherwise stated. Ether refers to diethyl ether. Solvents were obtained dry from Sigma Aldrich, Gillingham, UK or another appropriate chemical supplier and used as supplied. In cases where mixtures of solvents were utilised, the ratios refer to the volumes used. Reagents were used as supplied unless otherwise stated. Flash chromatography was carried out using silica gel 40–63 μ 60Å. Analytical thin layer chromatography (TLC) was performed using precoated aluminium or glass-backed plates (silica gel 60Å F₂₅₄) and visualised by UV radiation at 254 nm, or by staining with phosphomolybdic acid in ethanol or potassium permanganate in water. All melting points were determined using a Gallenkamp melting point apparatus and are uncorrected. Infrared spectra were recorded using a Diamond ATR (attenuated total reflection) accessory (Golden Gate) or as a solution in chloroform via transmission IR cells on a Bruker Tension 5 spectrometer. ¹H NMR spectra were recorded in deutero solvent on Bruker Avance III 300, Bruker Avance II 400, Bruker Avance III HD 500 or Bruker Avance III HD 700 instruments and are reported as follows; chemical shift δ (ppm) (number of protons, multiplicity, coupling constant J (Hz), assignment). Residual protic solvent CHCl₃ (δ_H = 7.26) or DMSO (δ_H = 2.50) were used as the internal reference. ¹³C NMR spectra were recorded using the central resonance of CDCl₃ (δ_C = 77.0 ppm) or DMSO (δ_C = 39.5 ppm) as the internal reference. All chemical shifts are quoted in parts per million relative to tetramethylsilane (δ_H = 0.00 ppm) and coupling constants are given in Hertz to the nearest 1 Hz. Assignment of spectra were carried out using COSY, HSQC, HMBC and NOESY experiments and all ¹H and ¹³C NMR for new compounds are provided for reference (Figure S2, Supporting Information). Electrospray mass spectra (ES) were obtained on a Micromass LCT mass spectrometer. High resolution mass spectra (HRMS) were obtained using a Thermo LTQ mass spectrometer (ES).

3.1. Chemistry

3.1.1. Standard Procedure A: Synthesis of Boc Amino Acid Hydrazides*

A solution of N-Boc amino acid (1.0 g, 5.5 mmol) in dichloromethane (DCM) (25 mL) was treated with N,N-Diisopropylethylamine (DIPEA) (1.2 equiv.) and N-aryl hydrazine (1.2 equiv.), followed by 4-(4,6-dimethoxy-1,3,5-triazin-2-yl)-4-methyl-morpholinium chloride (DMTMM) (1.2 equiv.), and the solution was stirred at room temperature for 3 h. The reaction was mixed with DCM (20 mL), and the organic layer was washed with sat. aq. NH₄Cl (20 mL), sat. aq. NaHCO₃ (20 mL) and brine (20 mL). The organic layer was dried over MgSO₄, filtered, evaporated and dried in vacuo to afford the desired N-Boc amino acid hydrazides.

*Compound 6 synthesis is previously reported [16].

3.1.2. Standard Procedure B: Creation of New Amino Acid Hydrazides

Stage 1

The corresponding N-Boc amino acid hydrazides (0.10 g, 0.29 mmol) were mixed with 4 M HCl in dioxane (3 mL) and stirred at room temperature for 1 h under nitrogen. The solvent was then removed in vacuo, and the resultant oil was dissolved in DCM (5 mL) and evaporated three times to afford the desired deprotected amino acid hydrazide, which was used directly in stage 2 without further purification.

Stage 2

Crude deprotected amino acid hydrazide (0.29 mmol) was dissolved in DCM (5 mL) and treated successively with the aryl carboxylic acid (1.3 equiv.) and DIPEA (2.0 equiv.), followed by DMTMM (1.2 equiv.) at room temperature under nitrogen. The reaction was stirred for 3 h, then diluted with DCM (15 mL). The organic layer was washed with sat. aq. NH₄Cl (20 mL), sat. aq. NaHCO₃ (20 mL) and brine (20 mL). The organic layer was dried over MgSO₄, filtered, evaporated and dried in vacuo. The resultant solid was triturated with CHCl₃ to afford the desired N-substituted amino acid hydrazide.

3.1.3. Boc-Protected Compounds

tert-butyl N-[(1S)-3-(methylsulfanyl)-1-{N′-[4-(trifluoromethyl)phenyl]hydrazine carbonyl}propyl]carbamate, 7, following the standard procedure A, Boc-Met-OH (0.2 g, 0.8 mmol) and 4-trifluoromethylphenylhydrazine were transformed following flash chromatography (DCM/EtOH/ sat. aq. NH₃ [400:8:1], [200:8:1] and [100:8:1]) to afford the title compound as a pale yellow solid (0.14 g, 44%); R_f 0.32 (DCM/EtOH/ sat. aq. NH₃ [200:8:1]); m.p. 102–108 °C; ν_max (ATR) 3321, 2984, 1680, 1662, 1515, 1327, 1306, 1156, 1102, 830, 589 cm⁻¹; δ_H (700 MHz, CDCl₃) 8.82 (1H, s, CONHNH), 7.41 (2H, d, J 8, Ar–H), 6.81 (2H, d, J 8, Ar–H), 6.53 (1H, s, CONHNH), 5.43 (1H, d, J 8, NHCHCO), 4.44 (1H, q, J 7, NHCHCO), 2.56 (2H, t, J 7, NHCH(CH₂CH₂SCH₃)), 2.09–2.14 (5H, m, NHCH(CH₂CH₂SCH₃), NHCH(CH₂CH₂SCH₃)), 1.49 (9H, s, (C(CH₃)₃); δ_C (700 MHz, CDCl₃) 172.4 (CHCONH), 156.1 (NHCOOC(CH₃)₃), 150.5 (Ar–C), 126.3 (Ar–C), 124.2 (1C, q, ¹J_C–F 270, CF₃), 122.7 (1C, q, ²J_C–F 32, ipso-Ar-CCF₃), 112.7 (Ar–C), 80.9 (NHCOO-C), 51.9 (NHCHCO), 30.9 (NHCH(CH₂CH₂SCH₃)), 30.24 (NHCH(CH₂CH₂SCH₃)), 28.3 (NHCOOC(CH₃)₃), 15.4 (NHCH(CH₂CH₂SCH₃)); m/z (ES⁺) 408 (MH⁺); HRMS (ES⁺) found MH⁺, 408.1573 (C₁₇H₂₅F₃N₃O₃S requires 408.1569).

tert-butyl (S)-(1-(2-(3-chlorophenyl)hydrazineyl)-1-oxopropan-2-yl)carbamate, 8, following the standard procedure A, Boc-Ala-OH (1.0 g, 5.3 mmol) and 3-chlorophenylhydrazine were transformed to afford the title compound as a deep-yellow solid (1.6 g, 97%); R_f 0.46 (DCM/EtOH/ sat. aq. NH₃ [200:8:1]); m.p. 110–114 °C; ν_max (ATR) 3428, 3278, 3078, 2979, 2933, 1678, 1504, 1367, 1158 cm⁻¹; δ_H (400 MHz, CDCl₃) 8.44 (1H, bs, CONHNH), 7.03 (1H, t, J 8, Ar–H), 6.76 (1H, d, J 8, Ar-CH), 6.71 (1H, t, J 2, Ar-CH), 6.60 (1H, d, J 8, Ar-CH), 5.07 (1H, bs, CONHCH), 4.22–4.19 (1H, m, CH), 1.39 (9H, s, (C(CH₃)₃)), 1.31 (3H, d, J 7, NHCHCH₃C=O); δ_C (400 MHz, CDCl₃) 192.7 (OC=ONH), 173.0 (CHC=ONHNH), 155.9 ((CH₃)₃COC=O), 149.1 (Ar–C), 135.0 (Ar–C), 130.2 (Ar-CH), 121.0 (Ar–C), 113.4 (Ar-CH), 111.69 (Ar-CH), 48.7 (NHCHC=O), 28.3 (C(CH₃)₃), 17.5 (NHCH(CH₃)CO); m/z (ES⁺) 314 ([³⁵Cl]MH⁺), 316 ([³⁷Cl]MH⁺); HRMS (ES⁺) found ([³⁵Cl]MH⁺), 314.1271 (C₁₄H₂₁N₃O₃³⁵Cl requires 314.1278).

tert-Butyl N-[(1S)-1-[N′-(3-chlorophenyl)hydrazinecarbonyl]-3-(methylsulfanyl)propyl] carbamate, 9, following the standard procedure A, Boc-Met-OH (0.2 g, 0.802 mmol) and 3-chlorophenylhydrazine were transformed following flash chromatography (DCM/EtOH/ sat. aq. NH₃ [400:8:1] and [200:8:1]) to afford the title compound as a pale yellow solid (0.16 g, 53%); R_f 0.30 (DCM/EtOH/ sat. aq. NH₃ [200:8:1]); m.p. 94–97 °C; ν_max (ATR) 3331, 3272, 2985, 1683, 1658, 1521, 1163, 768 cm⁻¹; δ_H (700 MHz, CDCl₃) 8.73 (1H, s, CONHNH), 7.10 (1H, t, J 8, Ar–H), 6.85 (1H, d, J 8, Ar–H), 6.80 (1H, s, Ar–H), 6.67 (1H, d, J 8, Ar–H), 6.34 (1H, bs, CONHNH), 5.42 (1H, d, J 8, NHCHCO), 4.43 (1H, q, J 7, NHCHCO), 2.57 (2H, t, J 7, NHCHCH₂CH₂SCH₃), 2.09–2.13 (5H, m, NHCHCH₂CH₂SCH₃, NHCHCH₂CH₂SCH₃), 1.47 (9H, s, C(CH₃)₃); δ_C (700 MHz, CDCl₃) 172.2 (CHCONH), 156.9 (NHCOO(CH₃)₃), 149.0 (Ar–C), 134.9 (Ar–C), 130.2 (Ar–C), 121.0 (Ar–C), 113.4 (Ar–C), 111.6 (Ar–C), 80.8 (NHCOOC(CH₃)₃), 51.9 (NHCHCO), 31.0 (NHCHCH₂CH₂SCH₃), 30.2 (NHCHCH₂CH₂SCH₃), 28.32 (NHCOOC(CH₃)₃), 15.5 (NHCHCH₂CH₂SCH₃); m/z (ES⁺) 374 ([³⁵Cl]MH⁺), 376 ([³⁷Cl]MH⁺), 396 ([³⁵Cl]MNa⁺), 398 ([³⁷Cl]MNa⁺); HRMS (ES⁺) found ([³⁵Cl]MNa⁺), 396.1141 (C₁₆H₂₄N₃O₃S³⁵ClNa requires 396.1125).

3.1.4. Final Compounds

(S)-N-(1-Oxo-1-(2-(4-(trifluoromethyl)phenyl)hydrazineyl)propan-2-yl)isonicotinamide, 10, following the standard procedure B, tert-butyl (S)-(1-oxo-1-(2-(4-(trifluoromethyl) phenyl)hydrazineyl)propan-2-yl)carbamate (0.10 g, 0.30 mmol) and isonicotinic acid were transformed to afford the title compound as a pale-yellow solid (76 mg, 72%); R_f 0.15 (DCM/EtOH/ sat. aq. NH₃ [200:8:1]); ν_max (ATR) 3261 (N–H), 3095, 2973 (C–H), 1638 (C=O), 1617, 1536, 1327 (C–F), 1158 (C–N), 1102, 1065 (C–F) cm⁻¹; δ_H (400 MHz, DMSO-d₆) 10.05 (1H, s, CONHNH), 8.98 (1H, d, J 7, PyCONH), 8.73 (2H, d, J 6, Py-H), 8.39 (1H, bs, CONHNH), 7.82 (2H, d, J 6, Py-H), 7.44 (2H, d, J 8, Ar–H), 6.83 (2H, d, J 8, Ar–H), 4.50 (1H, m, NHCH(CH₃)CO), 1.44 (3H, d, J 7, NHCH(CH₃)CO); δ_C (100 MHz, DMSO-d₆) 172.6 (CONHNH), 165.4 (PyCONH), 152.9 (ipso-Ar–C), 150.6 (Py-C), 141.4 (ipso-Py-C), 126.6 (Ar–C), 124.4 (1C, q, ¹J_C–F 270, CF₃), 122.0 (Py-C), 118.5 (1C, q, ²J_C–F 31, ipso-Ar-CCF₃), 111.9 (Ar–C), 48.7 (NHCH(CH₃)CO), 18.0 (NHCH(CH₃)CO); δ_F (282 MHz, DMSO-d₆) -59.28 (3F, s, CF₃); m/z (ES⁺) 353 (MH⁺); HRMS (ES⁺) found MH⁺, 353.1237 (C₁₆H₁₆F₃N₄O₂ requires 353.1225).

(S)-N-(4-(methylthio)-1-oxo-1-(2-(4-(trifluoromethyl)phenyl)hydrazineyl)butan-2-yl)isonicotinamide, 11, following the standard procedure B, tert-Butyl N-[(1S)-3-(methylsulfanyl)-1-{N′-[4-(trifluoromethyl)phenyl]hydrazine carbonyl}propyl]carbamate (0.14 g, 0.41 mmol) and isonicotinic acid were transformed to afford the title compound as a white solid (108 mg, 64%); m.p. 179–181 °C; ν_max (ATR) 3264, 1665, 1639, 1615, 1531, 1480, 1410, 1323, 1236, 1158, 1105, 1065, 1010, 878, 836, 757 cm⁻¹; δ_H (300 MHz, DMSO-d₆) 10.12 (1H, s, CONHNH), 8.98 (1H, d, J 7, PyCONH), 8.74 (2H, d, J 6, Py-H), 8.43 (1H, bs, CONHNH), 7.84 (2H, d, J 6, Py-H), 7.45 (2H, d, J 8, Ar–H), 6.82 (2H, d, J 8, Ar–H), 4.61 (1H, m, NHCH(CH₂CH₂SCH₃)), 2.67–2.53 (2H, m, NHCH(CH₂CH₂SCH₃)), 2.15–2.09 (5H, m, NHCH(CH₂CH₂SCH₃); δ_C (75 MHz, DMSO-d₆) 171.7 (CONHNH), 165.3 (PyCONH), 150.6 (Py-C), 126.6 (Ar–C), 122.1 (Py-C), 111.9 (Ar–C), 52.3 (NHCH(CH₂CH₂SCH₃)), 31.3 (NHCH(CH₂CH₂SCH₃)), 30.4 (NHCH(CH₂CH₂SCH₃)), 15.1 (NHCH(CH₂CH₂SCH₃)); δ_F (282 MHz, DMSO-d₆) -59.28 (3F, s, CF₃); m/z (ES⁺) 413 (MH⁺); HRMS (ES⁺) found MH⁺, 413.1261 (C₁₈H₂₀N₄O₂S requires 413.1259).

(S)-N-(1-(2-(3-chlorophenyl)hydrazineyl)-1-oxopropan-2-yl)isonicotinamide, 12, following the standard procedure B, tert-butyl (S)-(1-(2-(3-chlorophenyl)hydrazineyl)-1-oxopropan-2-yl)carbamate (0.10 g, 0.32 mmol) and isonicotinic acid were transformed to afford the title compound as a white solid (60 mg, 59%); R_f 0.13 (DCM/EtOH/ sat. aq. NH₃ [200:8:1]); ν_max (ATR) 3302, 3254 (N–H), 3035 (Ar–CH), 2983, 2930 (C–H), 1668, 1638 (C=O) 1599, 1537, 1511 (C=C) 1106 cm⁻¹; δ_H (400 MHz, DMSO-d₆) 9.97 (1H, s, CONHNH), 8.99 (1H, d, J 7, Py-CONH), 8.75 (2H, d, J 6, Py-H), 8.08 (1H, s, CONHNH), 7.84 (2H, d, J 6, Py-H), 7.14 (1H, t, J 8, Ar–H), 6.75–6.66 (3H, m, Ar–H), 4.53 (1H, m, NHCH(CH₃)CO), 1.44 (3H, d, J 7, NHCH(CH₃)CO); δ_C (100MHz, DMSO-d₆) 172.6 (CONHNH), 165.4 (Py-CO), 151.3 (ipso-Ar–C), 150.6 (Py-C), 141.3 (ipso-Py-C), 133.9 (ipso-Ar–C), 130.5 (Ar–C), 122.0 (Py-C), 118.3 (Ar–C), 111.9 (Ar–C), 111.3 (Ar–C), 48.7 (NHCH(CH₃)CO), 17.9 (NHCH(CH₃)CO); m/z (ES⁺) 319 ([³⁷Cl]MH⁺), 321 ([³⁵Cl]MH⁺); HRMS (ES⁺) found [³⁵Cl]MH⁺, 319.0962 (C₁₅H₁₆N₄O₂³⁵Cl requires 319.0962).

(S)-N-(1-(2-(3-chlorophenyl)hydrazineyl)-4-(methylthio)-1-oxobutan-2-yl)isonicotinamide, 13, following the standard procedure B, tert-Butyl N-[(1S)-1-[N′-(3-chlorophenyl)hydrazinecarbonyl]-3-(methylsulfanyl)propyl] carbamate (0.35 g, 1.13 mmol) and isonicotinic acid were transformed to afford the title compound as a brown solid (113 mg, 26%); m.p. 78–81 °C; ν_max (ATR) 3259, 2919, 1659, 1622, 1597, 0521, 1475, 1407, 1385, 1310, 1229, 1151, 1096, 1065, 992, 834 cm⁻¹; δ_H (300 MHz, DMSO-d₆) 10.03 (1H, s, CONHNH), 8.98 (1H, d, J 7, PyCONH), 8.75 (2H, d, J 6, Py-H), 8.09 (1H, bs, CONHNH), 7.84 (2H, d, J 6, Py-H), 7.15 (1H, t, J 8, Ar–H), 6.78–6.62 (3H, m, Ar–H), 4.60 (1H, m, NHCH(CH₂CH₂SCH₃)), 2.67–2.53 (2H, m, NHCH(CH₂CH₂SCH₃)), 2.09–1.98 (5H, m, NHCH(CH₂CH₂SCH₃); δ_C (75 MHz, DMSO-d₆) 171.6 (CONHNH), 165.8 (PyCONH), 151.3 (ipso-Ar–C), 150.6 (Py-C), 141.4 (ipso-Ar–C), 134.0 (ipso-Ar–C), 131.3 (ipso-Ar–C), 130.8 (Ar–C), 122.1 (Py-C), 118.3 (Ar–C), 111.9 (Ar–C), 52.3 (NHCH(CH₂CH₂SCH₃)), 31.2 (NHCH(CH₂CH₂SCH₃)), 30.4 (NHCH(CH₂CH₂SCH₃)), 15.1 (NHCH(CH₂CH₂SCH₃)); m/z (ES⁺) 379 ([³⁵Cl]MH⁺), 381 ([³⁷Cl]MH⁺); HRMS (ES⁺) found [³⁵Cl]MH⁺, 379.0994 (C₁₇H₂₀N₄O₂S³⁵Cl requires 379.0995).

(S)-N-(1-Oxo-1-(2-(4-(trifluoromethyl)phenyl)hydrazineyl)propan-2-yl)pyrazine-2-carboxamide, 14, following the standard procedure B, tert-butyl (S)-(1-oxo-1-(2-(4-(trifluoromethyl) phenyl)hydrazineyl)propan-2-yl)carbamate (0.10 g, 0.30 mmol) and pyrazinoic acid were transformed following flash chromatography (n-hexane/EtOAc [4:1] to afford the title compound as a white solid (54 mg, 52%); R_f 0.19 (DCM/EtOH/ sat. aq. NH₃ [200:8:1]); ν_max 3255 (N–H), 3098, 2981 (C–H), 1638 (C=O), 1617, 1534, 1326 (C–F), 1156 (C–N), 1101, 1065 (C–F) cm⁻¹; δ_H (400 MHz, DMSO-d₆) 10.10 (1H, bs, CONHNH), 9.22 (1H, s, Pyz-H), 8.91 (1H, m, Pyz-H), 8.87 (1H, d, J 8, PyzCONH), 8.77 (1H, d, J 2, Pyz-H), 8.43 (1H, bs, CONHNH), 7.48 (2H, d, J 8, Ar–H), 6.84 (2H, d, J 8, Ar–H), 4.60 (1H, m, NHCH(CH₃)CO), 1.50 (3H, d, J 7, NHCH(CH₃)CO); δ_C (100 MHz, DMSO-d₆) 172.2 (CONHNH), 163.1 (PyzCO), 152.8 (ipso-Ar–C), 148.2 (Pyz-C), 144.9 (ipso-Pyz-C), 143.99 (Pyz-C), 143.85 (Pyz-C), 126.6 (Ar–C), 123.3 (1C, q, ¹J_C–F 269, CF₃), 118.5 (1C, q, ²J_C–F 32, ipso-Ar-CCF₃), 111.9 (Ar–C), 47.9 (NHCH(CH₃)CO), 18.7 (NHCH(CH₃)CO); δ_F (282 MHz, DMSO-d₆) -59.31 (3F, s, CF₃); m/z (ES⁺) 354 (MH⁺); HRMS (ES⁺) found MH⁺, 354.1188 (C₁₅H₁₅F₃N₅O₂ requires 354.1178).

(S)-N-(4-(methylthio)-1-oxo-1-(2-(4-(trifluoromethyl)phenyl)hydrazineyl)butan-2-yl)pyrazine-2-carboxamide, 15, following the standard procedure B, tert-Butyl N-[(1S)-3-(methylsulfanyl)-1-{N′-[4-(trifluoromethyl)phenyl]hydrazine carbonyl}propyl]carbamate (78 mg, 0.23 mmol) and pyrazinoic acid were transformed to afford the title compound as a yellow semisolid (80 mg, 86%); ν_max (ATR) 3264, 1661, 1616, 1519, 1404, 1322, 1157, 1105, 1064, 1019, 838, 832, 771 cm⁻¹; δ_H (300 MHz, CDCl₃) 9.36 (1H, s, Pyz-H), 9.06 (1H, d, J 8, CONHNH), 8.78 (1H, d, J 2, Pyz-H), 8.53 (1H, bs, Pyz-H), 8.43 (1H, d, J 8, CONH), 7.40 (1H, d, J 8, Ar–H), 6.82 (1H, d, J 8, Ar–H), 4.99 (1H, m, NHCH(CH₂CH₂SCH₃)), 2.63 (2H, m, NHCH(CH₂CH₂SCH₃)), 2.35–2.10 (5H, m, NHCH(CH₂CH₂SCH₃); δ_C (100 MHz, CDCl₃) 171.2 (CONHNH), 163.7 (Pyz-CONH), 150.4 (ipso-Ar–C), 147.9 (Pyz-C), 145.0 (ipso-Pyz-C), 144.3 (Pyz-C), 143.4 (ipso-Ar–C), 142.8 (Pyz-C), 126.6 (Ar–C), 122.6 (1C, q, ²J_C–F 31, ipso-Ar-CCF₃), 112.5 (Ar–C), 50.7 (NHCH(CH₂CH₂SCH₃)), 30.94 (NHCH(CH₂CH₂SCH₃)), 30.15 (NHCH(CH₂CH₂SCH₃)), 15.4 (NHCH(CH₂CH₂SCH₃)); m/z (ES⁺) 414 (MH⁺); HRMS (ES⁺) found MH⁺, 414.1207 (C¹⁷H¹⁹F³N⁵O²S requires 414.1212).

(S)-N-(1-(2-(3-chlorophenyl)hydrazineyl)-1-oxopropan-2-yl)pyrazine-2-carboxamide, 16, following the standard procedure B, tert-butyl (S)-(1-(2-(3-chlorophenyl)hydrazineyl)-1-oxopropan-2-yl)carbamate (0.10 g, 0.32 mmol) and pyrazinoic acid were transformed to afford the title compound as a white solid (63 mg, 62%) as a mixture of rotamers [6:1]; R_f 0.21 (DCM/EtOH/ sat. aq. NH₃ [200:8:1]); ν_max (ATR) 3383, 3293 (N–H), 3029 (Ar-CH), 2922, 2865 (C–H), 1681, 1659 (C=O) 1596, 1536, 1092, 1018, 886 cm⁻¹; NMR data given for major rotamer δ_H (400 MHz, CDCl₃) 9.35 (1H, s, Pyz-H), 8.89 (1H, s, CONHNH), 8.76 (1H, d, J 2, Pyz-H), 8.53 (1H, m, Pyz-H), 8.34 (1H, d, J 8, Pyz-CONH), 7.06 (1H, dd, J 8, Ar–H), 6.79 (1H, d, J 8, Ar–H), 6.76 (1H, s, Ar–H), 6.65 (1H, d, J 8, Ar–H), 4.85 (1H, m, NHCH(CH₃)CO), 1.57 (3H, d, J 7, NHCH(CH₃)CO); δ_C (100 MHz, CDCl₃) 172.1 (CONHNH), 163.5 (Pyz-CONH), 149.0 (ipso-Ar–C), 147.8 (Pyz-C), 144.3 (Pyz-C), 143.6 (ipso-Pyz-C), 142.8 (Pyz-C), 135.0 (ipso-Ar–C), 130.2 (Ar–C), 121.1 (Ar–C), 113.4 (Ar–C), 111.7 (Ar–C), 47.58 (NHCH(CH₃)CO), 17.7 (NHCH(CH₃)CO); m/z (ES⁺) 320 ([³⁵Cl]MH⁺), 322 ([³⁷Cl]MH⁺); HRMS (ES⁺) found [³⁵Cl]MH⁺, 320.0914 (C₁₄H₁₅N₅O₂³⁵Cl requires 320.0914).

(S)-N-(1-(2-(3-chlorophenyl)hydrazineyl)-4-(methylthio)-1-oxobutan-2-yl)pyrazine-2-carboxamide, 17, following the standard procedure B, tert-Butyl N-[(1S)-1-[N′-(3-chlorophenyl)hydrazinecarbonyl]-3-(methylsulfanyl)propyl] carbamate (70 mg, 0.23 mmol) and pyrazinoic acid were transformed to afford the title compound as a white solid (61 mg, 71%); m.p. 99–102 °C; ν_max (ATR) 3333, 3290, 2921, 1708, 1678, 1652, 1596, 1585, 1523, 1482, 1438, 1425, 1404, 1375, 1318, 1299, 1272, 1234, 1221, 1188, 1163, 1114, 1091, 1071, 1052, 1023, 991, 958, 946, 914, 864, 809 cm⁻¹; δ_H (400 MHz, DMSO-d₆) 10.03 (1H, bs, CONHNH), 9.22 (1H, s, Pyz-H), 9.00 (1H, d, J 8, CONH), (1H, s, CONHNH), 8.91 (1H, d, J 2, Pyz-H), 8.78 (1H, bs, Pyz-H), 8.10 (1H, bs, CONHNH), 7.16 (1H, dd, J 8, Ar–H), 6.74–6.62 (3H, m, Ar–H), 4.70 (1H, m, NHCH(CH₂CH₂SCH₃)), 2.59–2.50 (2H, m, NHCH(CH₂CH₂SCH₃)), 2.18–2.03 (5H, m, NHCH(CH₂CH₂SCH₃); δ_C (75 MHz, DMSO-d₆) 171.2 (CONHNH), 163.7 (Pyz-CONH), 151.3 (ipso-Ar–C), 148.1 (Pyz-C), 145.0 (ipso-Pyz-C), 144.1 (Pyz-C), 143.8 (Pyz-C), 134.0 (ipso-Ar–C), 130.8 (Ar–C), 118.4 (Ar–C), 111.9 (Ar–C), 111.3 (Ar–C), 51.7 (NHCH(CH₂CH₂SCH₃)), 31.6 (NHCH(CH₂CH₂SCH₃)), 30.2 (NHCH(CH₂CH₂SCH₃)), 15.1 (NHCH(CH₂CH₂SCH₃)); m/z (ES⁺) 380 ([³⁵Cl]MH⁺), 382 ([³⁷Cl]MH⁺); HRMS (ES⁺) found [³⁵Cl]MH⁺, 380.0948 (C₁₆H₁₉³⁵ClN₅O₂S requires 380.0948).

(S)-N-(1-Oxo-1-(2-(4-(trifluoromethyl)phenyl)hydrazineyl)propan-2-yl)-2-naphthamide, 18, following the standard procedure B, tert-butyl (S)-(1-oxo-1-(2-(4-(trifluoromethyl) phenyl)hydrazineyl)propan-2-yl)carbamate (0.10 g, 0.29 mmol) and 2-napthoic acid were transformed to afford the title compound as a white solid (65 mg, 56%); R_f 0.24 (DCM/EtOH/ sat. aq. NH₃ [200:8:1]); ν_max (ATR) 3329, 3264 (N–H), 3051, 2995, 2854, 1674, 1618 (C=O), 1525, 1325 (C–F), 1160 (C–N), 1095, 1065 (C–F), 834 (C–C) cm⁻¹; δ_H (400 MHz, DMSO) 10.04 (1H, bs, CONHNH), 8.82 (1H, d, J 2, Np-CONH), 8.55 (1H, s, Np–H), 8.42 (1H, d, J 2, CONHNH), 8.08–7.97 (4H, m, Np–H), 7.66–7.58 (2H, m, Np–H), 7.47 (2H, d, J 8, Ar–H), 6.87 (2H, d, J 8, Ar–H), 4.60 (1H, m, NHCH(CH₃)), 1.49 (3H, d, J 7, NHCH(CH₃)); δ_C (176 MHz, DMSO-d₆) 173.1 (CONHNH), 166.9 (NpCONH), 153.0 (ipso-Ar–C), 134.7 (ipso-Ar–C), 132.5 (ipso-Ar–C), 131.7 (ipso-Ar–C), 129.3 (Np–C), 128.4 (Np–C), 128.4 (Np–C), 128.2 (Ar–C), 128.1 (Np–C), 127.2 (Np–C), 126.6 (Np–C), 125.0 (Np–C), 123.7 (1C, q, ¹J_C–F 269, CF₃), 118.6 (1C, q, ²J_C–F 31, ipso-Ar-CCF₃), 112.0 (Ar–C), 48.7 (NHCH(CH₃)), 18.2 (NHCH(CH₃)); δ_F (282 MHz, DMSO-d₆) -59.3 (3F, s, CF₃); m/z (ES⁺) 402 (MH⁺); HRMS (ES⁺) found MH⁺, 402.1427 (C₂₁H₁₉F₃N₃O₂ requires 402.1429).

(S)-N-(4-(methylthio)-1-oxo-1-(2-(4-(trifluoromethyl)phenyl)hydrazineyl)butan-2-yl)-2-naphthamide, 19, following the standard procedure B, tert-Butyl N-[(1S)-3-(methylsulfanyl)-1-{N′-[4-(trifluoromethyl)phenyl]hydrazine carbonyl}propyl]carbamate (65 mg, 0.19 mmol) and 2-naphthoic acid were transformed to afford the title compound as a white solid (53 mg, 61%); m.p. 163–166°C; ν_max (ATR) 3264, 1666, 1635, 1615, 1520, 1503, 1432, 1325, 1232, 1159, 1103, 1065, 1011, 955, 897, 865, 838 cm⁻¹; δ_H (300 MHz, DMSO-d₆) 10.12 (1H, bs, CONHNH), 8.83 (1H, d, J 7, Np-CONH), 8.56 (1H, s, Np–H), 8.44 (1H, bs, CONHNH), 8.10–7.94 (4H, m, Np–H), 7.65–7.55 (2H, m, Np–H), 7.60 (2H, d, J 8, Ar–H), 6.87 (1H, d, J 8, Ar–H), 4.69 (1H, m, NHCH(CH₂CH₂SCH₃)), 2.74–2.55 (2H, m, NHCH(CH₂CH₂SCH₃)), 2.19–2.06 (5H, m, NHCH(CH₂CH₂SCH₃); δ_C (75 MHz, DMSO-d₆) 172.1 (CONHNH), 167.4 (CONH), 152.9 (ipso-Ar–C), 134.7 (ipso-Ar–C), 134.0 (ipso-Ar–C), 132.5 (ipso-Ar–C), 131.8 (ipso-Ar–C), 129.3 (Np–C), 128.4 (Np–C), 128.2 (Np–C), 128.1 (Np–C), 127.2 (Np–C), 126.6 (Ar–C), 125.0 (Np–C), 118.8 (1C, q, ²J_C–F 32, ipso-Ar-CCF₃), 111.9 (Ar–C), 52.3 (NHCH(CH₂CH₂SCH₃)), 31.5 (NHCH(CH₂CH₂SCH₃)), 30.5 (NHCH(CH₂CH₂SCH₃)), 15.2 (NHCH(CH₂CH₂SCH₃)); δ_F (282 MHz, DMSO-d₆) 59.26 (3F, s, CF₃); m/z (ES⁺) 462 (MH⁺), 484 (MNa⁺); HRMS (ES⁺) found MH⁺, 462.1465 (C₂₃H₂₃F₃N₃O₂S requires 462.1463).

(S)-N-(1-(2-(3-chlorophenyl)hydrazineyl)-1-oxopropan-2-yl)-2-naphthamide, 20, following the standard procedure B, tert-butyl (S)-(1-(2-(3-chlorophenyl)hydrazineyl)-1-oxopropan-2-yl)carbamate (0.10 g, 0.32 mmol) and 2-napthoic acid were transformed to afford the title compound as a white solid (86 mg, 73%); R_f 0.32 (DCM/EtOH/ sat. aq. NH₃ [200:8:1]); ν_max (ATR) 3331, 3236 (NH), 3062 (Ar-CH), 2983, 2926 (CH), 1634, 1626 (C=O),1599, 1536, 1536 (C=C), 1334 (C–N) cm⁻¹; δ_H (400 MHz, DMSO-d₆) 9.96 (1H, bs, CONHNH), 8.82 (1H, d, J 7, Np-CONH), 8.56 (1H, s, Np–H), 8.07–7.95 (4H, m, Np–H), 7.67–7.57 (2H, m, Np–H), 7.14 (1H, dd, J 8, Ar–H), 6.77 (1H, t, J 2, Ar–H), 6.73–6.69 (2H, m, Ar–H), 4.58 (1H, m, NHCH(CH₃)CO), 1.47 (3H, d, J 7, NHCH(CH₃)CO); δ_C (100 MHz, DMSO-d₆) 173.0 (CHCONHNH), 166.9 (Np-CONH), 151.4 (Ar–C), 134.7 (Np–C), 134.0 (ipso-Ar–C), 132.5 (Np–C), 131.8 (Np–C), 130.8 (Ar–C), 129.3 (Np–C), 128.3 (Np–C), 128.2 (Np–C), 128.1 (Np–C), 127.2 (Np–C), 125.0 (Np–C), 118.2 (Ar–C), 111.9 (Ar–C), 111.3 (Ar–C), 48.7 (NHCH(CH₃)CO), 18.1 (NHCH(CH₃)CO); m/z (ES⁺) 368 (^[35Cl]MH⁺), 370 (^[37Cl]MH⁺); HRMS (ES⁺) found ([³⁵Cl]MH⁺, 368.1170 (C₂₀H₁₉N₃O₂³⁵Cl requires 368.1166).

(S)-N-(1-(2-(3-chlorophenyl)hydrazineyl)-4-(methylthio)-1-oxobutan-2-yl)-2-naphthamide, 21, following the standard procedure B, tert-Butyl N-[(1S)-1-[N′-(3-chlorophenyl)hydrazinecarbonyl]-3-(methylsulfanyl)propyl] carbamate (70 mg, 0.23 mmol) and 2-naphthoic acid were transformed to afford the title compound as a white solid (18 mg, 19%); m.p. 205–208 °C; ν_max (ATR) 3224, 1636, 1625, 1597, 1527, 1494, 1452, 1440, 1335, 1303, 1268, 1231, 1201, 1076, 989, 955, 892, 863, 839 cm⁻¹; δ_H (400 MHz, DMSO-d₆) 10.04 (1H, bs, CONHNH), 8.85 (1H, d, J 7, Np-CONH), 8.56 (1H, s, Np–H), 8.11 (1H, bs, CONHNH), 8.10–7.97 (4H, m, Np–H), 7.68–7.54 (2H, m, Np–H), 7.15 (1H, dd, J 8, Ar–H), 6.77 (1H, t, J 2, Ar–H), 6.73–6.65 (2H, m, Ar–H), 4.67 (1H, m, NHCH(CH₂CH₂SCH₃)), 2.68–2.56 (2H, m, NHCH(CH₂CH₂SCH₃)), 2.12–2.06 (5H, m, NHCH(CH₂CH₂SCH₃); δ_C (176 MHz, DMSO-d₆) 172.0 (CHCONHNH), 167.4 (Np-CONH), 151.4 (Ar–C), 134.7 (Np–C), 134.0 (ipso-Ar–C), 132.5 (Np–C), 131.8 (Np–C), 130.8 (Ar–C), 129.3 (Np–C), 128.3 (Np–C), 128.2 (Np–C), 128.1 (Np–C), 127.7 (Np–C), 125.0 (Np–C), 118.3 (Ar–C), 111.9 (Ar–C), 111.3 (Ar–C), 52.3 (NHCH(CH₂CH₂SCH₃)), 31.4 (NHCH(CH₂CH₂SCH₃)), 30.5 (NHCH(CH₂CH₂SCH₃)), 15.1 (NHCH(CH₂CH₂SCH₃)); m/z (ES⁺) 428 ([³⁵Cl]MH⁺), 430 ([³⁷Cl]MH⁺); HRMS (ES⁺) found [³⁵Cl]MH⁺, 428.1201 (C₂₂H₂₃³⁵ClN₃O₂S requires 428.1200).

(S)-N-(1-Oxo-1-(2-(4-(trifluoromethyl)phenyl)hydrazineyl)propan-2-yl)-1-naphthamide, 22, following the standard procedure B, tert-butyl (S)-(1-oxo-1-(2-(4-(trifluoromethyl) phenyl)hydrazineyl)propan-2-yl)carbamate (0.10 g, 0.29 mmol) and 1-napthoic acid were transformed to afford the title compound as a white solid (54 mg, 46%); R_f 0.24 (DCM/EtOH/ sat. aq. NH₃ [200:8:1]; ν_max (ATR) 3315, 3242 (N–H), 3074 (C–H), 2999, 2865 (C–H), 1667, 1633 (C=O), 1617, 1536, 1324 (C–F), 1159 (C–N), 1095, 1065 (C–F), 828, 787, 776 (C–C) cm⁻¹; δ_H (400 MHz, DMSO-d₆) 10.10 (1H, bs, CONHNH), 8.83 (1H, d, J 7, NpCONH), 8.47 (1H, bs, CONHNH), 8.28 (1H, d, J 8, Np–H), 8.03 (1H, d, J 8, Np–H), 7.98 (1H, d, J 8, Np–H) 7.68 (1H, d, J 7, Np–H), 7.59–7.50 (3H, m, Np–H), 7.47 (2H, d, J 8, Ar–H), 6.91 (2H, d, J 8, Ar–H), 4.60 (1H, m, NHCH(CH₃)CO), 1.44 (3H, d, J 7, NHCH(CH₃)CO); δ_C (100 MHz, DMSO-d₆) 173.1 (CONHNH), 167.3 (NpCONH), 153.0 (ipso-NHNHAr–C), 134.1 (Np–C), 134.0 (Np–C), 133.9 (Np–C), 130.2 (Np–C), 128.6 (Np–C), 126.9 (Np–C), 126.7 (Np–C), 126.6 (Ar–C), 126.1 (Np–C), 125.9 (Np–C), 125.3 (Np–C), 118.4 (1C, q, ²J_C–F 32, ipso-Ar-CCF₃), 112.0 (Ar–C), 48.5 (NHCH(CH₃)CO), 18.0 (NHCH(CH₃)CO); δ_F (282 MHz, DMSO-d₆) −59.25 (3F, s, CF₃); m/z (ES⁺) 402 (MH⁺); HRMS (ES⁺) found MH⁺, 402.1433 (C₂₁H₁₉F₃N₃O₂ requires 402.1429).

(S)-N-(4-(methylthio)-1-oxo-1-(2-(4-(trifluoromethyl)phenyl)hydrazineyl)butan-2-yl)-1-naphthamide, 23, following the standard procedure B, tert-Butyl N-[(1S)-3-(methylsulfanyl)-1-{N′-[4-(trifluoromethyl)phenyl]hydrazine carbonyl}propyl]carbamate (65 mg, 0.19 mmol) and 1-naphthoic acid were transformed to afford the title compound as a white solid (53 mg, 61%); m.p. 189–192 °C; ν_max (ATR) 3239, 1671, 1635, 1616, 1592, 1521, 1439, 1414, 1378, 1325, 1256, 1231, 1182, 1104, 1065, 1011, 966, 939, 886, 834 cm⁻¹; δ_H (300 MHz, DMSO-d₆) 10.18 (1H, bs, CONHNH), 8.86 (1H, d, J 7, NpCONH), 8.50 (1H, bs, CONHNH), 8.27 (1H, d, J 8, Np–H), 8.08–7.94 (2H, m, Np–H), 7.66–7.52 (3H, m, Np–H), 7.47 (2H, d, J 8, Ar–H), 6.92 (2H, d, J 8, Ar–H), 4.70 (1H, m, NHCH(CH₂CH₂SCH₃)), 2.74–2.55 (2H, m, NHCH(CH₂CH₂SCH₃)), 2.15–2.01 (5H, m, NHCH(CH₂CH₂SCH₃); δ_C (75 MHz, DMSO-d₆) 172.1 (CONHNH), 167.3 (NpCONH), 153.0 (ipso-Ar–C), 134.7 (ipso-Ar–C), 133.6 (ipso-Ar–C), 130.4 (ipso-Ar–C), 130.3 (Np–C), 128.6 (Np–C), 127.0 (Np–C), 126.7 (Ar–C), 126.5 (ipso-Ar–C), 126.1 (Np–C), 126.0 (Np–C), 125.4 (Np–C), 125.4 (Np–C), 118.3 (1C, q, ²J_C–F 31, ipso-Ar-CCF₃), 112.0 (Ar–C), 52.1 (NHCH(CH₂CH₂SCH₃)), 31.4 (NHCH(CH₂CH₂SCH₃)), 30.4 (NHCH(CH₂CH₂SCH₃)), 15.1 (NHCH(CH₂CH₂SCH₃)); δ_F (282 MHz, DMSO-d₆) 59.27 (3F, s, CF₃); m/z (ES⁺) 462 (MH⁺), 484 (MNa⁺); HRMS (ES⁺) found MH⁺, 462.1468 (C₂₃H₂₃F₃N₃O₂S requires 462.1463).

(S)-N-(1-(2-(3-chlorophenyl)hydrazineyl)-1-oxopropan-2-yl)-1-naphthamide, 24, following the standard procedure B, tert-butyl (S)-(1-(2-(3-chlorophenyl)hydrazineyl)-1-oxopropan-2-yl)carbamate (0.10 g, 0.32 mmol) and 1-napthoic acid were transformed to afford the title compound as a white solid (55 mg, 45%); ν_max (ATR) 3404, 3237 (NH), 3052 (Ar-CH), 2995, 2946 (CH), 1634 (C=O), 1595 (C=C), 1324 (C–N) cm⁻¹; δ_H (400 MHz, DMSO-d₆) 10.00 (1H, bs, CONHNH), 8.83 (1H, d, J 7, Np-CONH), 8.32 (1H, dd, J 8, 2, Np–H), 8.15 (1H, s, CONHNH), 8.03 (1H, d, J 8, Np–H), 7.98 (1H, dd, J 8, 2, Np–H), 7.68 (1H, d, J 8, Np–H), 7.60–7.50 (2H, m, Np–H), 7.16 (1H, dd, J 8, Ar–H), 6.83 (1H, bs, Ar–H), 6.76–6.71 (2H, m, Ar–H), 4.59 (1H, m, NHCH(CH₃)CO), 1.42 (3H, d, J 7, NHCH(CH₃)CO); δ_C (100 MHz, DMSO-d₆) 173.1 (CONHNH), 169.2 (Np-CONH), 151.4 (Ar–C), 134.6 (Np–C), 134.0 (Ar–C), 133.5 (Np–C), 130.8 (Ar–C), 130.3 (Np–C), 128.5 (Np–C), 127.0 (Np–C), 126.6 (Np–C), 126.2 (Np–C), 126.0 (Np–C), 125.3 (Np–C), 118.3 (Ar–C), 111.9 (Ar–C), 111.3 (Ar–C), 48.4 (NHCH(CH₃)CO), 18.0 (NHCH(CH₃)CO); m/z (ES⁺) 368 (^[35Cl]MH⁺), 370 (^[37Cl]MH⁺); HRMS (ES⁺) found ([³⁵Cl]MH⁺, 368.1170 (C₂₀H₁₉N₃O₂³⁵Cl requires 368.1166).

(S)-N-(1-(2-(3-chlorophenyl)hydrazineyl)-4-(methylthio)-1-oxobutan-2-yl)-1-naphthamide, 25, following the standard procedure B, tert-Butyl N-[(1S)-1-[N′-(3-chlorophenyl)hydrazinecarbonyl]-3-(methylsulfanyl)propyl] carbamate (70 mg, 0.23 mmol) and 1-naphthoic acid were transformed to afford the title compound as a pale yellow solid (54 mg, 56%); m.p. 183–186 °C; ν_max (ATR) 3239, 1667, 1635, 1594, 1524, 1471, 1435, 1313, 1255, 1216, 1074, 992, 885, 851, 765 cm⁻¹; δ_H (300 MHz, DMSO-d₆) 10.07 (1H, bs, CONHNH), 8.87 (1H, d, J 7, NpCONH), 8.27 (1H, d, J 8, Np–H), 8.15 (1H, bs, CONHNH), 8.05–7.93 (2H, m, Np–H), 7.69 (1H, m, Np–H), 7.63–7.50 (3H, m, Np–H), 7.17 (1H, t, J 6, Ar–H), 6.82 (1H, s, Ar–H), 6.76–6.70 (2H, m, Ar–H), 4.68 (1H, m, NHCH(CH₂CH₂SCH₃)), 2.70–2.58 (2H, m, NHCH(CH₂CH₂SCH₃)), 2.15–2.01 (5H, m, NHCH(CH₂CH₂SCH₃); δ_C (75 MHz, DMSO-d₆) 172.1 (CONHNH), 169.5 (NpCONH), 151.4 (ipso-Ar–C), 134.6 (ipso-Ar–C), 134.0 (ipso-Ar–C), 130.4 (ipso-Ar–C), 130.3 (Np–C), 128.6 (Np–C), 127.1 (Np–C), 126.7 (Ar–C), 126.7 (ipso-Ar–C), 126.1 (Np–C), 125.4 (Np–C), 118.3 (ipso-Ar–C), 112.0 (Ar–C), 111.4 (Ar–C), 52.1 (NHCH(CH₂CH₂SCH₃)), 31.4 (NHCH(CH₂CH₂SCH₃)), 30.4 (NHCH(CH₂CH₂SCH₃)), 15.1 (NHCH(CH₂CH₂SCH₃)); m/z (ES⁺) 428 ([³⁵Cl]MH⁺), 430 ([³⁷Cl]MH⁺); HRMS (ES⁺) found [³⁵Cl]MH⁺, 428.1192 (C₂₂H₂₃N₃O₂S³⁵Cl requires 428.1200).

(S)-N-(1-Oxo-1-(2-(4-(trifluoromethyl)phenyl)hydrazineyl)propan-2-yl)quinoline-3-carboxamide, 26, following the standard procedure B, tert-butyl (S)-(1-oxo-1-(2-(4-(trifluoromethyl) phenyl)hydrazineyl)propan-2-yl)carbamate (0.10 g, 0.30 mmol) and 3-quinolinecarboxylic acid were transformed to afford the title compound as a white solid (53 mg, 44%); R_f 0.15 (DCM/EtOH/ sat. aq. NH₃ [200:8:1]); ν_max (ATR) 3259 (N–H), 2998, 2935 (C–H), 1637, 1617 (C=O), 1522, 1450, 1325, 1158, 1103 1065 (C–F) cm⁻¹; δ_H (400 MHz, DMSO-d₆) 10.09 (1H, bs, CONHNH), 9.34 (1H, d, J 2, Quin-H), 9.06 (1H, d, J 7, QuinCONH), 8.93 (1H, s, Quin-H), 8.43 (1H, s, CONHNH), 8.11 (2H, m, Quin-H), 7.89 (1H, dd, J 8, Quin-H), 7.71 (1H, dd, J 8, Quin-H), 7.47 (2H, d, J 8, Ar–H), 6.87 (2H, d, J 8, Ar–H), 4.63 (1H, quin, J 7, NHCH(CH₃)CO), 1.50 (3H, d, J 7, NHCH(CH₃)CO); δ_C (100 MHz, DMSO-d₆) 172.8 (CONHNH), 165.6 (Quin-CO), 152.9 (ipso-Ar–C), 149.7 (Quin-C), 148.9 (ipso-Ar–C), 136.4 (Quin-C), 131.7 (Quin-C), 129.6 (ipso-Ar–C), 129.2 (Quin-C), 127.9 (Quin-C), 127.1 (ipso-Ar–C), 126.6 (ipso-Ar–C), 124.2 (1C, q, ¹J_C–F 272, Ar-CCF₃), 118.6 (1C, q, ²J_C–F 31, ipso-Ar-CCF₃), 111.9 (Ar–C), 48.8 (NHCH(CH₃)CO), 18.1 (NHCH(CH₃)CO); δ_F (282 MHz, DMSO-d₆) -59.28 (3F, s, CF₃); m/z (ES⁺) 403 (MH⁺); HRMS (ES⁺) found MH⁺, 403.1367 (C₂₀H₁₈F₃N₄O₂ requires 403.1382).

(S)-N-(4-(methylthio)-1-oxo-1-(2-(4-(trifluoromethyl)phenyl)hydrazineyl)butan-2-yl)quinoline-3-carboxamide, 27, following the standard procedure B, tert-Butyl N-[(1S)-3-(methylsulfanyl)-1-{N′-[4-(trifluoromethyl)phenyl]hydrazine carbonyl}propyl]carbamate (65 mg, 0.19 mmol) and 3-quinolinecarboxylic acid were transformed to afford the title compound as a beige solid (57 mg, 65%); m.p. 138–141 °C; ν_max (ATR) 3258, 3001, 1636, 1616, 1538, 1496, 1418, 1328, 1231, 1185, 1158, 1098, 1066, 1009, 959, 917, 902, 865, 832 cm⁻¹; δ_H (300 MHz, DMSO-d₆) 10.15 (1H, bs, CONHNH), 9.34 (1H, d, J 2, Quin-H), 9.06 (1H, d, J 7, QuinCONH), 8.93 (1H, s, Quin-H), 8.45 (1H, s, CONHNH), 8.12 (2H, m, Quin-H), 7.88 (1H, dd, J 8, Quin-H), 7.71 (1H, dd, J 8, Quin-H), 7.47 (2H, d, J 8, Ar–H), 6.85 (2H, d, J 8, Ar–H), 4.70 (1H, m, NHCH(CH₂CH₂SCH₃)), 2.75–2.56 (2H, m, NHCH(CH₂CH₂SCH₃)), 2.20–2.05 (5H, m, NHCH(CH₂CH₂SCH₃); δ_C (75 MHz, DMSO-d₆) 171.9 (CONHNH), 166.0 (Quin-CO), 152.9 (ipso-Ar–C), 149.7 (Quin-C), 148.9 (ipso-Ar–C), 136.4 (Quin-C), 131.7 (Quin-C), 129.6 (ipso-Ar–C), 129.3 (Quin-C), 127.9 (Quin-C), 127.1 (ipso-Ar–C), 126.9 (Ar–C), 123.7 (1C, q, ¹J_C–F 270, Ar-CCF₃), 118.6 (1C, q, ²J_C–F 31, ipso-Ar-CCF₃), 112.0 (Ar–C), 52.4 (NHCH(CH₂CH₂SCH₃)), 31.4 (NHCH(CH₂CH₂SCH₃)), 30.5 (NHCH(CH₂CH₂SCH₃)), 15.1 (NHCH(CH₂CH₂SCH₃)); δ_F (282 MHz, DMSO-d₆) -59.27 (3F, s, CF₃); m/z (ES⁺) 463 (MH⁺); HRMS (ES⁺) found MH⁺, 463.1416 (C₂₂H₂₂F₃N₄O₂S requires 463.1416).

(S)-N-(1-(2-(3-chlorophenyl)hydrazineyl)-1-oxopropan-2-yl)quinoline-3-carboxamide, 28, following the standard procedure B, tert-butyl (S)-(1-(2-(3-chlorophenyl)hydrazineyl)-1-oxopropan-2-yl)carbamate (0.10 g, 0.32 mmol) and 3-quinolinecarboxylic acid were transformed to afford the title compound as a white solid (37 mg, 30%); R_f 0.29 (DCM/EtOH/ sat. aq. NH₃ [200:8:1]); ν_max (ATR) 3324 (N–H), 2988, 2947 (C–H), 1646, 1613 (C=O), 1513 (C=N), 1151, 1103, 1065 (C–F) cm⁻¹; δ_H (400 MHz, DMSO-d₆) 10.00 (1H, bs, CONHNH), 9.35 (1H, d, J 2, Quin-NCH), 9.08 (1H, d, J 7, Quin-CONH), 8.93 (1H, s, Quin-CH), 8.15–8.07 (3H, m, Quin-CH, CONHNH), 7.89 (1H, t, J 8, Quin-CH), 7.72 (1H, t, J 8, Quin-CH), 7.15 (1H, t, J 8, Ar–H), 6.78 (1H, t, J 2, Ar–H), 6.71 (2H, m, Ar–H), 4.60 (1H, m, NHCH(CH₃)), 1.48 (3H, d, J 7, NHCH(CH₃)); δ_C (75 MHz, DMSO-d₆) 172.7 (CONHNH), 165.6 (Quin-CONH), 151.4 (ipso-Ar–C), 149.7 (Quin-C), 149.0 (ipso-Quin-C), 136.4 (Quin-C), 134.0 (ipso-Ar–C), 131.7 (Quin-C), 130.8 (Ar–C), 129.6 (Quin-C), 129.3 (Quin-C), 127.9 (Quin-C), 127.1 (ipso-Ar–C), 126.9 (ipso-Ar–C), 118.3 (Ar–C), 111.9 (Ar–C), 111.3 (Ar–C), 48.7 (NHCH(CH₃)), 18.1 (NHCH(CH₃)); m/z (ES⁺) 369 ([³⁵Cl]MH⁺), 371 ([³⁷Cl]MH⁺); HRMS (ES⁺) found [³⁵Cl]MH⁺, 369.1120 (C₁₉H₁₈N₄O₂³⁵Cl requires 369.1118).

(S)-N-(1-(2-(3-chlorophenyl)hydrazineyl)-4-(methylthio)-1-oxobutan-2-yl)quinoline-3-carboxamide, 29, following the standard procedure B, tert-Butyl N-[(1S)-1-[N′-(3-chlorophenyl)hydrazinecarbonyl]-3-(methylsulfanyl)propyl] carbamate (70 mg, 0.23 mmol) and 3-quinolinecarboxylic acid were transformed to afford the title compound as a white solid (68 mg, 71%); m.p. 141–144 °C; ν_max (ATR) 3211, 3029, 2913, 1664, 1638, 1595, 1570, 1534, 1492, 1424, 1374, 1307, 1272, 1229, 1203, 1155, 1136, 1112, 1080, 1019, 993, 981, 960, 948, 914, 900, 876, 855 cm⁻¹; δ_H (400 MHz, DMSO-d₆) 10.08 (1H, bs, CONHNH), 9.35 (1H, d, J 2, Quin-NCH), 9.07 (1H, d, J 7, Quin-CONH), 8.93 (1H, s, Quin-CH), 8.15–8.07 (3H, m, Quin-CH, CONHNH), 7.89 (1H, t, J 8, Quin-CH), 7.72 (1H, t, J 8, Quin-CH), 7.15 (1H, t, J 8, Ar–H), 6.77 (1H, t, J 2, Ar–H), 6.70 (2H, m, Ar–H), 4.67 (1H, m, NHCH(CH₂CH₂SCH₃)), 2.71–2.59 (2H, m, NHCH(CH₂CH₂SCH₃)), 2.16–2.06 (5H, m, NHCH(CH₂CH₂SCH₃); δ_C (75 MHz, DMSO-d₆) 171.8 (CONHNH), 166.0 (Quin-CONH), 151.4 (ipso-Ar–C), 149.7 (Quin-C), 149.0 (ipso-Quin-C), 136.4 (Quin-C), 134.0 (ipso-Ar–C), 131.7 (Quin-C), 130.8 (Ar–C), 129.6 (Quin-C), 129.3 (Quin-C), 127.9 (Quin-C), 127.1 (ipso-Ar–C), 126.9 (ipso-Ar–C), 118.3 (Ar–C), 111.9 (Ar–C), 111.4 (Ar–C), 52.4 (NHCH(CH₂CH₂SCH₃)), 31.4 (NHCH(CH₂CH₂SCH₃)), 30.4 (NHCH(CH₂CH₂SCH₃)), 15.1 (NHCH(CH₂CH₂SCH₃)); m/z (ES⁺) 429 ([³⁵Cl]MH⁺), 431 ([³⁷Cl]MH⁺); HRMS (ES⁺) found [³⁵Cl]MH⁺, 429.1148 (C₂₁H₂₂³⁵ClN₄O₂S requires 429.1152).

(S)-3,5-Dinitro-N-(1-oxo-1-(2-(4-(trifluoromethyl)phenyl)hydrazineyl)propan-2-yl)benzamide, 30, following the standard procedure B, tert-butyl (S)-(1-oxo-1-(2-(4-(trifluoromethyl) phenyl)hydrazineyl)propan-2-yl)carbamate (0.10 g, 0.30 mmol) and 3,5-dinitrobenzoic acid were transformed to afford the title compound as a white solid (79 mg, 60%); ν_max (ATR) 3250 (NH), 3101 (Ar-CH), 2896 (CH), 1641 (C=O), 1617 (Ar C–C), 1535, 1342, 1330, 1160, 1107, 1066 (C–F) cm⁻¹; δ_H (400 MHz, DMSO-d₆) 10.13 (1H, bs, CONHNH), 9.47 (1H, d, J 7, ArCONH), 9.14 (2H, d, J 2, Ar–H), 8.98 (1H, dd, J 2, Ar–H), 8.43 (1H, bs, CONHNH), 7.47 (2H, d, J 8, Ar–H), 6.84 (2H, d, J 8, Ar–H), 4.61 (1H, m, NHCH(CH₃)CO), 1.49 (3H, d, J 7, NHCH(CH₃)CO); δ_C (100 MHz, DMSO-d₆) 172.4 (CONHNH), 163.0 (ArCONH), 152.9 (ipso-Ar–C), 148.6 (ipso-Ar–C), 137.1 (ipso-Ar–C), 128.4 (Ar–C), 126.7 (Ar–C), 121.5 (Ar–C), 111.9 (Ar–C), 49.2 (NHCH(CH₃)CO), 18.0 (NHCH(CH₃)CO); δ_F (282 MHz, DMSO-d₆) -59.34 (3F, s, CF₃); m/z (ES⁺) 442 (MH⁺); HRMS (ES⁺) found MH⁺, 442.0958 (C₁₇H₁₅F₃N₅O₆ requires 442.0974).

(S)-N-(4-(methylthio)-1-oxo-1-(2-(4-(trifluoromethyl)phenyl)hydrazineyl)butan-2-yl)-3,5-dinitrobenzamide, 31, following the standard procedure B, tert-Butyl N-[(1S)-3-(methylsulfanyl)-1-{N′-[4-(trifluoromethyl)phenyl]hydrazine carbonyl}propyl]carbamate (65 mg, 0.19 mmol) and 3,5-dinitrobenzoic acid were transformed to afford the title compound as a beige solid (36 mg, 38%); m.p. 97–100 °C; ν_max (ATR) 3464, 3212, 3125, 3075, 1662, 1633, 1614, 1541, 1440, 1342, 1322, 1251, 1162, 1115, 1063, 1010, 933, 837 cm⁻¹; δ_H (300 MHz, DMSO-d₆) 10.20 (1H, bs, CONHNH), 9.45 (1H, d, J 7, ArCONH), 9.15 (2H, d, J 2, Ar–H), 8.99 (1H, dd, J 2, Ar–H), 8.44 (1H, bs, CONHNH), 7.47 (2H, d, J 8, Ar–H), 6.84 (2H, d, J 8, Ar–H), 4.68 (1H, m, NHCH(CH₂CH₂SCH₃)), 2.74–2.53 (2H, m, NHCH(CH₂CH₂SCH₃)), 2.19–2.04 (5H, m, NHCH(CH₂CH₂SCH₃); δ_C (75 MHz, DMSO-d₆) 171.4 (CONHNH), 163.4 (ArCONH), 152.8 (ipso-Ar–C), 148.6 (ipso-Ar–C), 137.0 (ipso-Ar–C), 128.5 (Ar–C), 127.3 (ipso-Ar–C), 126.6 (Ar–C), 121.5 (Ar–C), 118.7 (1C, q, ²J_C–F 32, ipso-Ar-CCF₃), 111.9 (Ar–C), 52.7 (NHCH(CH₂CH₂SCH₃)), 31.2 (NHCH(CH₂CH₂SCH₃)), 30.4 (NHCH(CH₂CH₂SCH₃)), 15.1 (NHCH(CH₂CH₂SCH₃)); δ_F (282 MHz, DMSO-d₆) -59.30 (3F, s, CF₃); m/z (ES⁺) 502 (MH⁺); HRMS (ES⁺) found MH⁺, 502.1010 (C₁₉H₁₉F₃N₅O₆S requires 502.1008).

(S)-N-(1-(2-(3-chlorophenyl)hydrazineyl)-1-oxopropan-2-yl)-3,5-dinitrobenzamide, 32, following the standard procedure B, tert-butyl (S)-(1-(2-(3-chlorophenyl)hydrazineyl)-1-oxopropan-2-yl)carbamate (0.10 g, 0.32 mmol) and 3,5-dinitrobenzoic acid were transformed to afford the title compound as a light brown solid (54 mg, 42%); R_f 0.21 (DCM/EtOH/ sat. aq. NH₃ [200:8:1]); ν_max (ATR) 3264 (NH), 3094 (Ar-CH), 2983, 2926 (CH), 1651, 1597 (C=O), 1537, 1342 (N–O), 1334 (C=C) cm⁻¹; δ_H (300 MHz, DMSO-d₆) 10.05 (1H, bs, CONHNH), 9.48 (1H, d, J 7, ArCONH), 9.15 (2H, d, J 2, Ar–H), 8.99 (1H, m, Ar–H), 8.10 (1H, bs, CONHNH), 7.14 (1H, t, J 8, Ar–H), 6.76 (1H, t, J 2, Ar–H), 6.73–6.66 (2H, m, Ar–H), 4.57 (1H, m, NHCH(CH₃)CO), 1.48 (3H, d, J 7, NHCH(CH₃)CO); δ_C (100 MHz, DMSO-d₆) 172.3 (CONHNH), 163.0 (ArCONH), 151.3 (ipso-Ar–C), 148.5 (ipso-Ar–C), 137.1 (ipso-Ar–C), 134.0 (ipso-Ar–C), 130.7 (Ar–C), 128.4 (Ar–C), 118.3 (Ar–C), 111.9 (Ar–C), 111.3 (Ar–C), 49.2 (NHCH(CH₃)CO), 17.9 (NHCH(CH₃)CO); m/z (ES⁺) 408 ([³⁵Cl]MH⁺), 410 ([³⁷Cl]MH⁺); HRMS (ES⁺) found [³⁵Cl]MH⁺, 408.0701 (C₁₆H₁₅N₅O₆³⁵Cl requires 408.0711).

(S)-N-(1-(2-(3-chlorophenyl)hydrazineyl)-4-(methylthio)-1-oxobutan-2-yl)-3,5-dinitrobenzamide, 33, following the standard procedure B, tert-Butyl N-[(1S)-1-[N′-(3-chlorophenyl)hydrazinecarbonyl]-3-(methylsulfanyl)propyl] carbamate (100 mg, 0.32 mmol) and 3,5-dinitrobenzoic acid were transformed to afford the title compound as a light brown gum (149 mg, 99%); m.p. 87–89 °C; ν_max (ATR) 3259, 3071, 1649, 1640, 1596, 1536, 1476, 1341, 1340, 1320, 1076, 1041, 918, 847 cm⁻¹; δ_H (300 MHz, DMSO-d₆) 10.12 (1H, bs, CONHNH), 9.44 (1H, d, J 7, ArCONH), 9.15 (2H, d, J 2, Ar–H), 8.99 (1H, dd, J 2, Ar–H), 8.10 (1H, bs, CONHNH), 7.15 (1H, t, J 8, Ar–H), 6.78–6.62 (3H, m, Ar–H), 4.68 (1H, m, NHCH(CH₂CH₂SCH₃)), 2.74–2.53 (2H, m, NHCH(CH₂CH₂SCH₃)), 2.19–2.04 (5H, m, NHCH(CH₂CH₂SCH₃); δ_C (75 MHz, DMSO-d₆) 171.4 (CONHNH), 163.4 (ArCONH), 151.2 (ipso-Ar–C), 148.6 (ipso-Ar–C), 137.1 (ipso-Ar–C), 134.0 (ipso-Ar–C), 130.7 (Ar–C), 128.5 (Ar–C), 121.3 (Ar–C), 118.5 (Ar–C), 111.9 (Ar–C), 111.3 (Ar–C), 52.8 (NHCH(CH₂CH₂SCH₃)), 31.2 (NHCH(CH₂CH₂SCH₃)), 30.4 (NHCH(CH₂CH₂SCH₃)), 15.1 (NHCH(CH₂CH₂SCH₃)); m/z (ES⁺) 468 ([³⁵Cl]MH⁺), 470 ([³⁷Cl]MH⁺); HRMS (ES⁺) found [³⁵Cl]MH⁺, 468.0743 (C₁₈H₁₉³⁵ClN₅O₆S requires 468.0745).

(S)-6-chloro-2-ethyl-N-(1-oxo-1-(2-(4-(trifluoromethyl)phenyl)hydrazineyl)propan-2-yl)imidazo[1,2-a]pyridine-3-carboxamide, 34, following the standard procedure B, tert-butyl (S)-(1-oxo-1-(2-(4-(trifluoromethyl) phenyl)hydrazineyl)propan-2-yl)carbamate (0.1 g, 0.35 mmol) and 6-chloro-2-ethylimidazo[1,2-a]pyridine-3-carboxylic acid were transformed to afford the title compound as a pale yellow solid (69 mg, 43%); m.p. 221–224 °C; ν_max. (ATR) 3252, 2967, 2932, 1667, 1609, 1541, 1522, 1493, 1453, 1442, 1391, 1329, 1281, 1251, 1220, 1160, 1097, 1066, 1009, 995, 952, 906 cm⁻¹; δ_H (400 MHz, DMSO-d₆) 10.10 (1H, d, J 2, CONHNH), 9.01 (1H, d, J 2, Ar–H), 8.47 (1H, d, J 2, CONHNH), 8.33 (1H, d, J 7, NHCH(CH₃)CO), 7.68 (1H, d, J 9, Ar–H), 7.51–7.45 (3H, m, Ar–H), 6.91 (2H, d, J 8, Ar–H), 4.60 (1H, q, J 7, NHCH(CH₃)CO), 3.00 (2H, q, J 7, CH₂CH₃), 1.46 (3H, d, J 7, NHCH(CH₃)CO), 1.26 (3H, t, J 7, CH₂CH₃); δ_C (100 MHz, DMSO-d₆) 172.8 (CONHNH), 161.1 (CONH), 153.0 (ipso-Ar–C), 151.8 (ipso-Ar–C), 143.7 (ipso-Ar–C), 127.5 (ipso-Ar–C), 126.6 (Ar–C), 125.2 (Ar–C), 120.1 (ipso-Ar–C), 117.7 (Ar–C), 112.0 (Ar–C), 48.3 (NHCH(CH₃)CO), 22.2 (CH₂CH₃), 18.2 (NHCH(CH₃)CO), 13.5 (CH₂CH₃); m/z (ES⁺) 454 ([³⁵Cl]MH⁺), 456 ([³⁷Cl]MH⁺); HRMS (ES⁺) found [³⁵Cl]MH⁺, 454.1256 (C₂₀H₂₀³⁵ClF₃N₅O₂ requires 454.1258).

(S)-6-chloro-2-ethyl-N-(4-(methylthio)-1-oxo-1-(2-(4-(trifluoromethyl)phenyl)hydrazineyl)butan-2-yl)imidazo[1,2-a]pyridine-3-carboxamide, 35, following the standard procedure B, tert-Butyl N-[(1S)-3-(methylsulfanyl)-1-{N′-[4-(trifluoromethyl)phenyl]hydrazine carbonyl}propyl]carbamate (65 mg, 0.19 mmol) and 6-chloro-2-ethylimidazo[1,2-a]pyridine-3-carboxylic acid were transformed to afford the title compound as a white solid (53 mg, 55%); m.p. 227–230 °C; ν_max (ATR) 3248, 1664, 1612, 1526, 1487, 1417, 1394, 1374, 1328, 1291, 1189, 1158, 1108, 1066, 1013, 1000, 924, 897, 838 cm⁻¹; δ_H (300 MHz, DMSO-d₆) 10.16 (1H, d, J 2, CONHNH), 8.96 (1H, d, J 2, Ar–H), 8.48 (1H, d, J 2, CONHNH), 8.42 (1H, d, J 7, ArCONH), 7.67 (1H, d, J 9, Ar–H), 7.52–7.45 (3H, m, Ar–H), 6.92 (2H, d, J 8, Ar–H), 4.70 (1H, m, NHCH(CH₂CH₂SCH₃)), 3.00 (2H, q, J 7, CH₂CH₃), 2.75–2.56 (2H, m, NHCH(CH₂CH₂SCH₃)), 2.20–2.05 (5H, m, NHCH(CH₂CH₂SCH₃), 1.28 (3H, t, J 7, CH₂CH₃); δ_C (75 MHz, DMSO-d₆) 171.9 (CONHNH), 161.6 (CONH), 152.9 (ipso-Ar–C), 151.8 (ipso-Ar–C), 143.7 (ipso-Ar–C), 127.5 (ipso-Ar–C), 126.5 (Ar–C), 125.1 (Ar–C), 120.1 (ipso-Ar–C), 117.7 (Ar–C), 116.3 (ipso-Ar–C), 112.0 (Ar–C), 52.4 (NHCH(CH₂CH₂SCH₃)), 31.2 (NHCH(CH₂CH₂SCH₃)), 30.4 (NHCH(CH₂CH₂SCH₃)), 22.2 (CH₂CH₃), 15.1 (NHCH(CH₂CH₂SCH₃)), 13.4 (CH₂CH₃); δ_F (282 MHz, DMSO-d₆) -59.32 (3F, s, CF₃); m/z (ES⁺) 514 ([³⁵Cl]MH⁺), 516 ([³⁷Cl]MH⁺); HRMS (ES⁺) found [³⁵Cl]MH⁺, 514.1290 (C₂₂H₂₄³⁵ClF₃N₅O₂S requires 514.1291).

(S)-6-chloro-N-(1-(2-(3-chlorophenyl)hydrazineyl)-1-oxopropan-2-yl)-2-ethylimidazo[1,2-a]pyridine-3-carboxamide, 36, following the standard procedure B, tert-butyl (S)-(1-(2-(3-chlorophenyl)hydrazineyl)-1-oxopropan-2-yl)carbamate (0.1 g, 0.4 mmol) and 6-chloro-2-ethylimidazo[1,2-a]pyridine-3-carboxylic acid were transformed to afford the title compound as a white solid (28 mg, 17%); m.p. 213–215 °C; ν_max. (ATR) 3258, 2978, 1666, 1608, 1605, 1538, 1492, 1455, 1417, 1394, 1370, 1317, 1269, 1248, 1218, 1159, 1139, 1110, 1075, 1044, 993, 950, 906, 850, 802 cm⁻¹; δ_H (400 MHz, DMSO-d₆) 10.00 (1H, d, J 2, CONHNH), 9.07 (1H, d, J 2, Ar–H), 8.31 (1H, d, J 7, NHCH(CH₃)CO), 8.13 (1H, d, J 2, CONHNH), 7.68 (1H, d, J 9, Ar–H), 7.48 (1H, dd, J 9, 2, Ar–H), 7.15 (1H, t, J 6, Ar–H), 6.85 (1H, s, Ar–H), 6.74–6.70 (2H, m, Ar–H), 4.54 (1H, q, J 7, NHCH(CH₃)CO), 3.00 (2H, q, J 7, CH₂CH₃), 1.46 (3H, d, J 7, NHCH(CH₃)CO), 1.28 (3H, t, J 7, CH₂CH₃); δ_C (100 MHz, DMSO-d₆) 172.8 (CONHNH), 161.1 (CONH), 151.9 (ipso-Ar–C), 151.3 (ipso-Ar–C), 143.7 (ipso-Ar–C), 134.1 (ipso-Ar–C), 130.7 (Ar–C), 127.6 (Ar–C), 125.3 (Ar–C), 120.1 (ipso-Ar–C), 118.3 (ipso-Ar–C), 117.7 (Ar–C), 116.3 (ipso-Ar–C), 112.0 (Ar–C), 111.4 (Ar–C), 48.3 (NHCH(CH₃)CO), 22.2 (CH₂CH₃), 18.1 (NHCH(CH₃)CO), 13.4 (CH₂CH₃); m/z (ES⁺) 420 ([^35,35Cl]MH⁺), 422 ([^35,37Cl]MH⁺), 424 ([^37,37Cl]MH⁺); HRMS (ES⁺) found [^35,35Cl]MH⁺, 420.0992 (C₁₉H₂₀^35,35Cl₂N₅O₂ requires 420.0994).

(S)-6-chloro-N-(1-(2-(3-chlorophenyl)hydrazineyl)-4-(methylthio)-1-oxobutan-2-yl)-2-ethylimidazo[1,2-a]pyridine-3-carboxamide, 37, following the standard procedure B, tert-Butyl N-[(1S)-1-[N′-(3-chlorophenyl)hydrazinecarbonyl]-3-(methylsulfanyl)propyl] carbamate (70 mg, 0.23 mmol) and 6-chloro-2-ethylimidazo[1,2-a]pyridine-3-carboxylic acid were transformed to afford the title compound as a white solid (20 mg, 18%); m.p. 188–191 °C; ν_max (ATR) 3334, 2916, 1666, 1603, 1519, 1489, 1417, 1396, 1341, 1305, 1288, 1212, 1151, 1120, 1048, 998, 963, 872, 847, 814 cm⁻¹; δ_H (400 MHz, DMSO-d₆) 10.07 (1H, d, J 2, CONHNH), 9.04 (1H, d, J 2, Ar–H), 8.41 (1H, d, J 7, CONH), 8.15 (1H, d, J 2, CONHNH), 7.70 (1H, d, J 9, Ar–H), 7.48 (1H, dd, J 9, 2, Ar–H), 7.16 (1H, t, J 6, Ar–H), 6.86 (1H, s, Ar–H), 6.76–6.68 (2H, m, Ar–H), 4.59 (1H, q, J 7, NHCH(CH₂CH₂SCH₃)), 3.00 (2H, q, J 7, CH₂CH₃), 2.68–2.56 (2H, m, NHCH(CH₂CH₂SCH₃)), 2.12–2.06 (5H, m, NHCH(CH₂CH₂SCH₃), 1.28 (3H, t, J 7, CH₂CH₃); δ_C (176 MHz, DMSO-d₆) 172.0 (CONHNH), 161.6 (CONH), 152.0 (ipso-Ar–C), 151.3 (ipso-Ar–C), 143.8 (ipso-Ar–C), 134.1 (ipso-Ar–C), 130.7 (Ar–C), 127.6 (Ar–C), 125.3 (Ar–C), 120.1 (ipso-Ar–C), 118.3 (ipso-Ar–C), 117.7 (Ar–C), 116.4 (ipso-Ar–C), 112.0 (Ar–C), 111.4 (Ar–C), 52.0 (NHCH(CH₂CH₂SCH₃)), 31.2 (NHCH(CH₂CH₂SCH₃)), 31.1 (NHCH(CH₂CH₂SCH₃)), 22.3 (CH₂CH₃), 15.1 (NHCH(CH₂CH₂SCH₃)), 13.6 (CH₂CH₃); m/z (ES⁺) 480 ([^35,35Cl]MH⁺), 482 ([^35,37Cl]MH⁺), 484 ([^37,37Cl]MH⁺); HRMS (ES⁺) found [^35,35Cl]MH⁺, 480.1026 (C₂₁H₂₄^35,35Cl₂N₅O₂S requires 480.1028).

3.2. Biological Assessment

3.2.1. Cell Lines

The bacterial species and cell lines used in this study can be found in

Table 2. Results of synthesis of the substituted amino acid hydrazides and the antibacterial activity and cytotoxicity.

Strain	Genotype	Comments	Reference
Mtb mc27000	ΔRD1(esx1):GFP ΔpanCD	Deletion of esx1 or RD1 responsible for virulence factor secretion, ESAT-6 and CFP-10 replaced with GFP. Pantothenate auxotroph.	W. Jacobs, Albert Einstein College of Medicine [32]
Mbv BCG	ΔRD1-14, 17-20	Bacillus Calmette–Guérin (BCG) Pasteur; Vaccine strain.	[33]
Mtb mc27000 pMV261	ΔRD1(esx1):GFP ΔpanCD; Kan R	As Mtb mc27000, contains pMV261 empty vector.	This study [34]
Mbv BCG pMV261	ΔRD1-14, 17-20; Kan R	As Mbv BCG, contains pMV261 empty vector.	This study [34]
Mtb AKB7002	ΔRD1(esx1):GFP ΔpanCD; Kan R rpoB (H445Y)	As Mtb mc27000 pMV261, generated spontaneous mutant, rifampicin-resistant, rpoB His445→Lys.	This study
Mtb AKB7021	ΔRD1(esx1):GFP ΔpanCD; Kan R katG (S315N)	As Mtb mc27000 pMV261, generated spontaneous mutant, isoniazid-resistant, katG Ser315→Asp.	This study

Kan ^R = Kanamycin resistant strain.

.

The cell line utilized for cytotoxicity studies were the murine macrophage cell line RAW264.7 (ATCC TIB-71).

3.2.2. Bacterial Growth Conditions

Mycobacterial species were cultured in either Middlebrook 7H9 broth or Middlebrook 7H10 agar media supplemented with albumin–dextrose–catalase (ADC) or oleic acid–albumin–dextrose–catalase (OADC) enrichments and 0.2% glycerol, 0.2% casamino acids, 24 μg/mL pantothenate, 1 μg/mL penicillin G, 10 μg/mL cyclohexamide, purchased from BD Biosciences. All reagents were purchased from Sigma-Aldrich, Gillingham, UK unless stated otherwise.

3.2.3. Spontaneous Mutant Generation

Mtb mc²7000 mono-resistant mutants were generated by plating 1 × 10⁸ mid-log cells on solid media (7H11 agar supplemented with 10% OADC and 0.2% glycerol, 0.2% casamino acids, 24 μg/mL pantothenate, 1 μg/mL penicillin G, 10 μg/mL cyclohexamide) containing 0.1, 0.2, 0.4, 1.6 and 3.2 μg/mL of RIF or INH. Plates were incubated at 37 °C, 5% CO₂ until the growth of colonies was visible. Spontaneous resistant mutants were confirmed by minimum inhibitory concentration (MIC) testing in liquid media as described below (REMA). The genomic DNA from validated mutants was extracted, and Next Generation Sequencing (NGS) analysis was performed to confirm mutation locations.

3.2.4. Bacterial Growth Inhibition Assays

Bacterial minimum inhibition concentrations (MIC) were determined using the resazurin microtiter assay (REMA) method, according to Palomino et al. [35]. Stock solutions of the tested compounds were prepared in sterile dimethyl sulfoxide (DMSO), then diluted in Middlebrook 7H9 broth (Difco, Detroit, MI, USA) supplemented with oleic acid, albumin, dextrose and catalase (OADC enrichment) to obtain a final compound concentration range of 0.0625–64 μg/mL. A suspension of the test Mycobacterium was cultured in Middlebrook 7H9 broth supplemented with 10% OADC and 0.2% glycerol, 0.2% casamino acids, 24 μg/mL pantothenate, 1 μg/mL penicillin G, 10 μg/mL cyclohexamide and 0.05% Tween 80 for one week at 37 °C in an atmosphere of 5% CO₂. The concentration was adjusted at McFarland 0.5 and diluted to 1 × 10⁶ CFU/mL and diluted in growth media 1:25. A 100 μL of the inoculum was added to each well of a 96-well microplate together with 100 μL of the compounds. The plate was incubated at 37 °C in an atmosphere of 5% CO₂. After 5 days, 10 μL 0.2% (w/v) resazurin (solubilized in sterile water) was added. MIC₉₉ was defined as the lowest concentration resulting in 99% inhibition of growth of Mycobacterium resulting in no colour change. Samples were set up in quadruplet and tested in two independent assays.

3.2.5. Determination of Cytotoxicity of Compounds against Mammalian Macrophages

RAW 264.7 cell lines were purchased from American Type Culture Collection, Middlesex, UK (ATCC1 TIB-71™). Cells were cultured in DMEM high glucose medium, supplemented with 10% FBS, 2 mM L-Glutamine and 1% penicillin/streptomycin, at 37 °C in a humidified incubator containing 5% CO₂. Cells were passaged after reaching 90% confluence.

Cells, in logarithmic growth, were plated in 96-well plates at a density of 1 × 10⁴ cells/well in 200 µL of media and incubated for 24 h. The media on the cells was removed and replaced with 180 µL of fresh media. To each respective well, 20 µL of test compound at a concentration of 1 mM was added, resulting in a final compound concentration of 100 µM. To control wells, DMSO drug solvent was added. In all wells, the final concentration of DMSO did not exceed 0.1%. Following incubation for a further 96 h at 37 °C in a humidified incubator containing 5% CO₂, all media was removed and replaced with 100 µL of fresh media. To each well, 20 µL of 3-(4,5-dimethylthiazol-2-yl)-5-(3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium, inner salt (MTS) assay solution (Promega, Madison, WI, USA) was added, and the plate was incubated in the dark at 37 °C for 4 h. Finally, the absorbance of each well was recorded at 490 nm using a microplate reader. The percentage of cell viability was calculated relevant to the compound solvent (DMSO) control.

4. Conclusions

With the end TB strategy faltering and the pipeline for new TB drugs being minimal, the requirement for novel architectures to combat the rise in drug-resistant TB infections is of paramount importance. The existing benzoxa-[2,1,3]-diazole amino acid hydrazide scaffolds were modified in order to demonstrate that the removal of the benzoxa-[2,1,3]-diazole moiety and replacement, utilising a scaffold hopping approach with relevant pharmacophores from existing anti-tubercular drugs, was a feasible tactic. The use of known chemical moieties present in molecules with anti-TB activity, such as quinoline or imidazo [1,2-a]pyridine-3-carboxy substituents, have provided a variety of antibacterial activities similar or greater to that with the benzoxa-[2,1,3]-diazole moiety and molecules with defined selectivity against drug-resistant strains of Mtb (Table 1 and [16]). In addition, the greater antibacterial activity observed between 3-chlorophenyl-substituted hydrazides compared to the 4-trifluorophenyl-substituted hydrazides remains to be elucidated; however, this may indicate a preferential binding pocket in the target site, favouring meta-substituted aromatic rings.

Overall, N-substituted amino acid hydrazides have provided a versatile scaffold for elaboration with known pharmacophores from existing drugs to provide active and clinically translatable anti-tubercular drugs. Whilst the exact mechanism of action is not understood, phenotypic observations have shown that these compounds favour isoniazid-resistant Mtb strains and so may target a pathway upstream of the site of INH activity or one involving perturbation of the ETC within mycobacteria. This hypothesis is yet to be tested and is currently under investigation.