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ORIGINAL RESEARCH article

Front. Chem., 14 June 2019
Sec. Organic Chemistry
This article is part of the Research Topic Isocyanide-based Multicomponent Reactions View all 10 articles

Isocyanide Reactions Toward the Synthesis of 3-(Oxazol-5-yl)Quinoline-2-Carboxamides and 5-(2-Tosylquinolin-3-yl)Oxazole

\nZahra YasaeiZahra YasaeiZeinab MohammadpourZeinab MohammadpourMorteza Shiri
Morteza Shiri*Zahra TanbakouchianZahra TanbakouchianShima FazelzadehShima Fazelzadeh
  • Department of Chemistry, Faculty of Physics and Chemistry, Alzahra University, Tehran, Iran

A palladium-catalyzed three-component reaction between 5-(2-chloroquinolin-3-yl) oxazoles, isocyanides, and water to yield 3-(oxazol-5-yl)quinoline-2-carboxamides is described. Interestingly, sulfonylation occurred when the same reaction was performed with toluenesulfonylmethyl isocyanide (TosMIC) as an isocyanide source. The reaction with 5-(2-chloroquinolin-3-yl)oxazoles and TosMIC in the presence of Cs2CO3 in DMSO afforded 5-(2-Tosylquinolin-3-yl)oxazoles. In basic media, TosMIC probably decomposed to generate Ts species, which were replaced with Cl. Tandem oxazole formation with subsequent sulfonylation of 2-chloroquinoline-3-carbaldehydes to form directly 5-(2-tosylquinolin-3-yl)oxazoles was also investigated.

Introduction

Quinolines are heterocyclic compounds exhibiting diverse and well-documented bioactivity and physical properties as well as existing as scaffolds in complex structures of natural products (Michael, 2002; Hranjec et al., 2017). Accordingly, quinoline synthesis, and functionalization has attracted much attention from synthetic organic chemists (Marco-Contelles et al., 2009; Shiri et al., 2011; Prajapati et al., 2014; Sharma et al., 2018; Nainwal et al., 2019).

However, isocyanides play an important role in synthesizing N-containing heterocycles and are particularly widely applied in Ugi and Passirini reactions (Domling and Ugi, 2000; Domling, 2006). Amides are especially valuable as precursors in synthesizing of bioactive and natural structures, in medicinal chemistry as well as protein synthesis (Bode, 2006; Rönn et al., 2008).

Many natural products such as urukthapelstatin A have been isolated from marine sources, these contains, several aminocarbonyl and oxazole functional groups with cytotoxic activity against human lung cancer (Yu et al., 2009). Similarly, venturamides A and B showed in vitro antimalarial activity (Linington et al., 2007; Davyt and Serra, 2010). Additionally, aerucyclamid C, a hexameric cyclopeptide, extremely active against T. brucei rhodesiense, which causes sleeping sickness, and exhibits lower activity against P. falciparum, the deadliest species of Plasmodium, which causes malaria (Davyt and Serra, 2010). Microcyclamide A is a cyclic hexapeptide with three five-membered heterocycles. It is isolated from cyanobacterium M. aeruginosa, and it has exhibited cytotoxic effects against P388 murine leukemia (Ishida et al., 2000; Davyt and Serra, 2010; Raveh et al., 2010) (Figure 1).

FIGURE 1
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Figure 1. Several natural products with amide and oxazole moieties.

Classical procedures for amide bond formation include reactions between carboxylic acids and amines (Linington et al., 2007; Davyt and Serra, 2010). Another route involves reactions of acyl halides, acyl azides, acyl imidazoles, anhydrides, or esters (activated carboxylic acid species) with amines (Ulijn et al., 2002; Montalbetti and Falque, 2005). As well as classical routes for amides synthesis which have own merits and demerits, direct aminocarbonylation from aryl halides in metal-catalyzed reactions has attracted attention from chemists due to its significant advantages benzamide preparation (Åkerbladh et al., 2017). In this regard, many synthetic methods have been introduced, including copper-catalyzed reactions of aryl halides and isocyanides in DMSO (Yavari et al., 2014). A palladium-catalyzed reaction was developed for amidation of aryl halides (Jiang et al., 2011), as well as the synthesis of 4-aminophthalazin-1(2H)-ones in a palladium-catalyzed reaction with isocyanide insertion in a multi-component reaction, which is difficult to achieve via a classical route (Vlaar et al., 2011). Palladium-catalyzed isocyanide insertion was applied to a carboxamidation/hydroamidation reaction to synthesize isoindolin-1-one derivatives (Pathare et al., 2016). Another example is the synthesis of isoquinolin-1(2H)-one derivatives via a palladium-catalyzed cascade reaction from isocyanide and amides (Wang et al., 2002; Tyagi et al., 2012; Chaudhary et al., 2013). Very recently, Guan et al reported an efficient method for the synthesis of multisubstituted 1H-imidazo-[4,5-c]quinoline derivatives via sequential van Leusen/Staudinger/aza-Wittig/carbodiimide-mediated cyclization (Guan et al., 2018).

Materials and Methods

General

The solvents and chemicals purchased from Merck and Aldrich chemical companies. Unless otherwise mentioned they used without further purification. Melting points are taken on an Electrothermal 9100 apparatus and are uncorrected. IR spectras recorded on a Shimadzu Infra-Red Spectroscopy IR-435. Nuclear magnetic resonance (NMR) spectra recorded on a Bruker AVANCE Spectrometer (400 MHz for 1H, 100 MHz for 13C) in DMSO-d6 and CDCl3 as solvent, TMS used as internal standard. The elemental analysis carried out with a Leco CHNS model 932. Mass spectra recorded on Agilent Technology (HP) 5973 Network Mass Selective Detector operating at an ionization potential of 70 eV.

The Typical Procedure for the Synthesis of 5-(2-chloroquinolin-3-yl)oxazole 3a

A mixture of 2-chloro-quinoline-3-carbaldehyde 2a (191 mg, 1.0 mmol), p-toluenesulfonylmethyl isocyanide 1 (234 mg, 1.2 mmol) and K2CO3 (341 mg, 2.5 equiv.) was added to EtOH (5.0 ml) and stirred for 3.5 h, at room temperature. After completion of the reaction, monitored by TLC, the mixture poured into cool water and stirred for 30 min. The product 3a filtered, washed with water two times and dried on the air.

The Typical Procedure for the Synthesis of N-cyclohexyl-3-(oxazol-5-yl)quinoline-2-carboxamide 5a

A mixture of 5-(2-chloroquinolin-3-yl)oxazole 3a (230 mg, 1.0 mmol), of Pd(OAc)2 (11 mg, 5 mol%) and Cs2CO3 (325 mg, 1.0 mmol) stirred in DMSO:H2O, 9:1 (5 mL) at 80°C for 15 min. Cyclohexyl isocyanide 4a (120 mg, 1.1 mmol) was added and the reaction stirred for 4 h. After completion of the reaction (the progress of the reaction was monitored by TLC) organic layer was extracted by DCM, washed with brine, dried over Na2SO4 and its solvent evaporated on a rotary evaporator. The residue was washed with 2-propanol and recrystallized in methanol to give 5a. It is noteworthy that 5a and 5h purified by washing with 2-propanol but other derivatives were purified by a column chromatography (n-hexan: ethyl acetate 3:1) and recrystallized in EtOH.

The Typical Procedure for the Synthesis of 5-(2-tosylquinolin-3-yl)oxazole 6a-e

A mixture of 2-chloro-quinoline-3-carbaldehyde 2a (191 mg, 1.0 mmol), p-toluenesulfonylmethyl isocyanide 1 (468 mg, 2.4 mmol) and Cs2CO3 (810 mg, equiv.) was added to DMSO (5.0 ml) and stirred for 5 h at 80°C. After completion of the reaction and monitored by TLC, the mixture poured into cool water and stirred for 30 min, then extracted with DCM. The product 6a purified by a column chromatography (n-hexan: ethyl acetate 4:1).

Supplementary Material

N-Cyclohexyl-3-(oxazol-5-yl) quinolone-2-carboxamide (5a)

Copies of NMR spectra are provided as Supplementary Materials. White powder, mp.: 123–128°C. 1H-NMR (400 MHz, CDCl3): δ = 1.25–1.52 (m, 5H), 1.68–171 (m, 1H), 1.80–1.85 (m, 2H), 2.10–213 (m, 2H), 3.99–4.02 (m, 1H), 7.60 (s, 1H), 7.67 (t, J = 8.0 Hz, 2H), 7.82 (t, J = 7.8 Hz, 1H), 7.90 (d, J = 8.4 Hz, 1H), 8.03 (s, 1H), 8.14 (d, J = 8.4 Hz, 1H), 8.44 (s, 1H) ppm. 13C-NMR (100 MHz, CDCl3): δ = 25.0, 25.6, 33.0, 48.6, 120.4, 125.9, 127.9, 128.0, 128.6, 129.5 131.0, 137.9, 145.9, 148.5, 148.8, 151.0, 164.3 ppm. Mass: m/z 321 (M+) (calcd. For C19H19N3O2: 321.37). FT-IR (KBr): νmax: 1604, 3444 cm−1. Anal. calcd. for C19H19N3O2: C, 71.01; H, 5.96; N, 13.08. Found: C,71.10; H,5.81; N,13.17.

N-Cyclohexyl-8-methyl-3-(oxazol-5-yl)quinolone-2-carboxamide (5b)

White powder, mp: 181–185°C. 1H-NMR (400 MHz, DMSO-d6): δ = 1.15–1.74 (m, 10H), 2.75 (s, 3H), 3.83 (m, 1H), 7.52 (s, 1H), 7.63 (d, J = 8.0 Hz, 1H), 7.73 (d, J = 6.8 Hz, 1H), 7.97 (d, J = 8.0 Hz, 1H), 8.60 (s, 1H), 8.74 (s, 1H) ppm. 13C-NMR (100 MHz, DMSO-d6): δ = 17.8, 25.0, 25.6, 25.8, 32.5, 33.8, 48.5, 118.6, 121.8, 125.0, 126.7, 127.6, 128.3, 131.4, 135.2, 136.9, 145.0, 147.8, 153.0, 167.0 ppm. Mass: m/z 335 (M+) (calcd. for C20H21N3O2: 335.40). FT-IR (KBr): νmax: 1646, 2853, 2922, 3310, 3444 cm−1. Anal. calcd. for C20H21N3O2: C, 71.62; H, 6.31; N, 12.53%. Found: C, 71.55; H, 6.47; N, 12.42%.

N-Butyl-6-methyl-3-(oxazol-5-yl)quinoline-2-carboxamide (5c)

White powder, mp: 124–127°C. 1H-NMR (400 MHz, CDCl3): δ = 1.01 (t, J = 7.2 Hz, 3H), 1.45–1.54 (m, 2H), 1.67–1.74 (m, 2H), 2.61 (s, 3H), 3.53 (dd, J = 13.4 Hz, J = 6.8 Hz, 2H), 7.60 (s, 1H), 7.65 (s, 1H), 7.68 (s, 1H), 7.77 (s, 1H), 8.03 (t, J = 5.2 Hz, 2H), 8.37 (s, 1H) ppm. 13C-NMR (100 MHz, CDCl3): δ = 13.8, 20.2, 21.8, 31.7, 39.5, 120.4, 125.7, 125.8, 126.5, 126.6, 128.1, 129.0, 133.4, 137.2, 138.9, 142.9, 150.9, 165.2 ppm. Mass: m/z 309 (M+) (calcd for C18H19N3O2: 309.36). FT-IR (KBr): νmax: 1542, 1652, 2858, 2928, 2956, 2922, 3114, 3299 cm−1. Anal. calcd. for: C18H19N3O2, C, 69.88; H, 6.19; N, 13.58%. Found C, 67.03; H, 6.24; N, 13.65%.

N-Cyclohexyl-6-methoxy-3-(oxazol-5-yl)quinoline-2-carboxamide (5d)

White powder, mp: 157–162°C. 1H-NMR (400 MHz, DMSO-d6): δ = 1.04–1.27 (m, 5H), 1.57–1.74 (m, 5H), 3.93(s, 3H), 3.93 (m, 1H), 7.52 (dd, J = 9.2, J = 2.8 Hz, 1H), 7.61 (d, J = 2.8 Hz, 1H), 7.92 (d, J = 9.2 Hz, 1H), 7.96 (s, 1H), 8.71 (s, 1H), 8.77 (s,1H) ppm. 13C-NMR (100 MHz, DMSO-d6): δ = 24.9, 25.8, 30.8, 31.2, 33.8, 47.9, 56.2, 106.7, 115.8, 121.3, 124.6, 127.5, 128.3, 129.6, 135.9, 142.4, 143.1, 146.5, 153.4, 158.7 ppm. Mass: m/z 351 (M+) (calcd. for C20H21N3O3:351.40). FT-IR (KBr): νmax: 1666, 2927, 2966, 3286, 3423 cm−1. Anal. calcd. for C20H21N3O3: C, 68.36; H, 6.02; N, 11.96%. Found: C, 68.47; H, 6.14; N, 12.11%.

N-Cyclohexyl-3-(oxazol-5-yl)benzo[h]quinoline-2-carboxamide (5e)

White powder, mp: 224–267°C. 1H-NMR (400 MHz, CDCl3): δ = 1.28–1.58 (m, 6H), 1.85–1.88 (m, 2H), 2.16–2.19 (m, 2H), 4.07- 4.10 (m, 1H), 7.30 (s, 1H), 7.74 (d, J = 2.4 Hz, 1H), 7.79-7.85 (m, 3H), 7.93 (d, J = 8.8 Hz, 1H), 7.97 (d, J = 7.6 Hz, 1H), 8.07 (s, 1H), 8.49 (s, 1H), 9.19 (d, J = 7.6 Hz, 1H) ppm. 13C-NMR (100 MHz, CDCl3): δ = 24.9, 25.7, 29.7, 33.2, 48.5, 77.2, 121.3, 124.3, 124.7, 126.6, 126.9, 127.7, 128.2, 129.1, 130.1, 130.6, 134.1, 137.5, 144.2, 146.7, 148.5, 151.1, 164.5 ppm. Mass: m/z 371 (M+) (calcd for C23H21N3O2:371.43). FT-IR (KBr): νmax: 1646, 2852, 2936, 3119, 3294, 3448 cm−1. Anal. calcd. for: C23H21N3O2, C, 74.37; H, 5.70; N, 11.31%. Found: C, 74.29; H, 5.84; N, 11.52%.

6-Chloro-N-cyclohexyl-3-(oxazol-5-yl)quinoline-2-carboxamide (5f)

White powder, mp: 226–232°C. 1H-NMR (400 MHz, CDCl3): δ = 1.25–1.52 (m, 5H), 1.68–1.83 (m, 3H), 2.09–2.12 (m, 2H), 3.94–4.04 (m, 1H), 7.54 (d, J = 8.0 Hz, 1H), 7.63 (s, 1H), 7.71 (dd, J = 9.0 Hz, J = 2.4 Hz, 1H), 7.86 (d, J = 2.4 Hz, 1H), 8.02 (s, 1H), 8.05 (d, J = 9.2 Hz, 1H), 8.34 (s, 1H) ppm. 13C-NMR (100 MHz, CDCl3): δ = 24.9, 25.6, 33.0, 48.7, 77.3, 121.2, 126.4, 126.6, 128.5, 131.0, 131.9, 134.5, 136.3, 144.1, 147.9, 149.0, 151.2, 164.2 ppm. Mass: m/z 355 (M+) (calcd. for C19H18 ClN3O2: 355.82). FT-IR (KBr): νmax: 663, 1649, 2852, 2923, 3279, 3443 cm−1. Anal. calcd. for: C19H18ClN3O2, C, 64.13; H, 5.10; N, 11.81%. Found: C, 64.20; H, 5.16; N, 11.70%.

N-(tert-Butyl)-6-chloro-3-(oxazol-5-yl)quinoline-2-carboxamide (5g)

White powder, mp: 190–197°C. 1H-NMR (400 MHz, DMSO-d6): δ = 1.43 (s, 9H), 7.75 (s, 1H), 7.86 (dd, J = 9.2 Hz, J = 2.4 Hz, 1H), 8.14 (d, J = 8.8 Hz, 1H), 8.28 (d, J = 2.4 Hz, 1H), 8.46 (s, 1H), 8.64 (s, 1H), 8.76 (s, 1H) ppm. 13C-NMR (100 MHz, DMSO-d6): δ = 28.8, 51.5, 119.5, 125.5, 127.4, 128.3, 131.3, 131.8, 132.7, 133.8, 144.5, 147.4, 153.4, 167.1 ppm. Mass: m/z 329.78 (M+) (calcd. for C17H16N3O2: 329.09). FT-IR (KBr): νmax: 1626, 2852, 2928, 3334, 3423 cm−1. Anal. calcd. for C17H16 ClN3O2: C, 61.91; H, 4.89; N, 12.74. Found: C, 62.04; H, 4.95; N, 12.89.

N-(tert-Butyl)-3-(oxazol-5-yl)quinolone-2-carboxamide (5h)

White powder, mp: 102–106°C. 1H-NMR (400 MHz, DMSO-d6): δ = 1.43 (s, 9H), 7.56 (s, 1H), 7.72 (t, J = 7.4 Hz, 1H), 7.87 (t, J = 7.6 Hz, 1H), 8.13 (t, J = 8.8 Hz, 2H), 8.41 (s, 1H), 8.61(s, 1H), 8.77 (s, 1H) ppm. 13C-NMR (100 MHz, DMSO-d6): δ = 28.8, 51.4, 118.7, 125.1, 127.5, 128.4, 128.8, 129.1, 131.4, 134.7, 146.0, 147.8, 153.0, 153.1, 167.4 ppm. Mass: m/z 295 (M+) (calcd. for C17H17N3O2: 295.34). FT-IR (KBr): νmax: 1658, 2904, 2966, 3422 cm−1. Anal. calcd. for C17H17N3O2: C, 69.14; H, 5.80; N, 14.23%. Found: C, 69.20; H, 5.87; N, 14.35%.

5-(2-Tosylquinolin-3-yl)oxazole (6a)

White powder, mp: 149–152°C. 1H-NMR (400 MHz, DMSO-d6): δ = 2.46 (s, 3H), 7.50 (d, J = 7.2 Hz, 2H), 7.77–7.90 (m, 6H), 8.18 (d, J = 7.6 Hz, 1H), 8.69 (s, 1H), 8.92 (s, 1H) ppm. 13C-NMR (100 MHz, DMSO-d6): δ = 21.6, 118.2, 127.6, 128.2, 128.9, 129.5, 129.6, 130.1, 130.6, 132.9, 135.5, 141.1, 144.9, 145.3, 145.6, 153.4, 155.1 ppm. Mass: m/z 350 (M+) (calcd for C19H14N2O3S:350.39). FT-IR (KBr): νmax: 683, 1073, 1103, 2851, 2920 cm−1. Anal. calcd. for: C19H14N2O3S, C, 65.13; H, 4.03; N, 7.99; S, 9.15%. Found: C, 65.23; H, 4.14; N, 8.06; S, 9.21%.

5-(8-Methyl-2-tosylquinolin-3-yl)oxazole (6b)

White powder, mp: 162–167°C. 1H-NMR (400 MHz, DMSO-d6): δ = 2.18 (s, 3H), 2.50 (s, 3H), 7.55 (d, J = 8.0 Hz, 1H), 7.71 (d, J = 6.8 Hz, 2H), 7.88 (s, 1H), 7.90 (d, J = 7.6 Hz, 2H), 8.03 (dd, J = 6.8 Hz, J = 2.8 Hz, 1H), 8.73 (s, 1H), 8.95 (s, 1H) ppm. 13C-NMR (100 MHz, DMSO-d6): δ = 16.5, 21.7, 117.5, 126.6, 127.7, 128.3, 129.9, 130.1, 130.4, 132.5, 135.3, 137.4, 140.3, 143.5, 145.3, 145.5, 153.6, 153.8 ppm. Mass: m/z 364 (M+) (calcd for C20H16N2O3S:364.42). FT-IR (KBr): νmax: 1294, 1379, 2852, 2922 cm−1. Anal. calcd. for: C20H16N2O3S, C, 65.92; H, 4.43; N, 7.69; S, 8.80%. Found: C, 66.03; H, 4.49; N, 7.78; S, 8.93%.

5-(6-Methyl-2-tosylquinolin-3-yl)oxazole (6c)

White powder, mp: 124–127°C. 1H-NMR (400 MHz, CDCl3): δ = 2.51 (s, 3H), 2.59 (s, 3H), 7.30 (s, 1H), 7.38 (d, J = 6.4 Hz, 2H), 7.62 (d, J = 8.4 Hz, 1H), 7.68 (s, 1H), 7.84 (d, J = 8.0 Hz, 1H), 7.89 (d, J = 7.6 Hz, 2H), 8.10 (s, 1H), 8.44 (s, 1H) ppm. 13C-NMR (100 MHz, DMSO-d6): δ = 21.6, 21.7, 118.3, 127.3, 127.5, 128.2, 129.2, 129.5, 130.0, 135.1, 135.7, 140.2, 140.8, 142.9, 143.6, 145.2, 145.7, 153.3 ppm. Mass: m/z 364 (M+) (calcd for C20H16N2O3S:364.42). FT-IR (KBr): νmax: 823, 1375, 2853, 2923 cm−1. Anal. calcd. for: C20H16N2O3S, C, 65.92; H, 4.43; N, 7.69; S, 8.80%. Found: C, 65.98; H, 4.49; N, 7.77; S, 8.86%.

5-(6-Methoxy-2-tosylquinolin-3-yl)oxazole (6d)

White powder, mp: 187–190°C. 1H-NMR (400 MHz, CDCl3): δ = 2.51 (s, 3H), 3.99 (s, 3H), 7.16 (d, J = 8.8 Hz, 2H), 7.30 (s, 1H), 7.39 (s, 1H), 7.58 (d, J = 8.8 Hz, 2H), 7.84 (d, J = 9.2 Hz, 2H), 7.90 (d, J = 8.4 Hz, 1H), 8.10 (s, 1H), 8.42 (s, 1H) ppm. 13C-NMR (100 MHz, CDCl3): δ = 37.1, 55.8, 104.6, 119.1, 124.0, 124.4, 124.8, 129.2, 129.6, 131.6, 135.6, 137.5, 138.4, 138.5, 144.5, 147.1, 147.6, 147.7 ppm. Mass: m/z 380 (M+) (calcd for C20H16N2O4S: 380.42). FT-IR (KBr): νmax: 1037, 117, 2850, 2920 cm−1. Anal. calcd. for: C20H16N2O4S, C, 63.14; H, 4.24; N, 7.36; S, 8.43%. Found: C, 63.21; H, 4.29; N, 7.43; S, 8.55%.

5-(2-Tosylbenzo[h]quinolin-3-yl)oxazole (6e)

White powder, mp: 202–207°C. 1H-NMR (400 MHz, CDCl3): δ = 2.60 (s, 3H), 7.30 (s, 1H), 7.52 (d, J = 8.0 Hz, 2H), 7.57 (t, J = 7.2 Hz, 1H), 7.70 (t, J = 6.8 Hz, 1H), 7.73 (d, J = 8.8 Hz, 1H), 7.89 (d, J = 8.4 Hz, 1H), 7.92 (d, J = 9.2 Hz, 1H), 8.04 (d, J = 8.4 Hz, 2H), 8.16 (d, J = 5.6 Hz, 1H), 8.20 (d, J = 8.4 Hz, 1H), 8.60 (s, 1H) ppm. 13C-NMR (100 MHz, CDCl3): δ = 21.8, 119.0, 124.1, 124.4, 127.0, 127.8, 128.0, 128.7, 129.3, 129.3, 130.2, 130.5, 131.1, 134.0, 135.3, 137.5, 134.3, 144.8, 145.5, 151.6, 153.3 ppm. Mass: m/z 400 (M+) (calcd for C23H16N2O3S: 400.45). FT-IR (KBr): νmax: 1313, 1400, 2853, 2920 cm−1. Anal. calcd. for: C23H16N2O3S, C, 68.98; H, 4.03; N, 7.00; S, 8.01%. Found: 69.06; H, 4.11; N, 7.12; S, 8.14%.

Results and Discussion

In continuation of our interest in quinoline chemistry (Shiri et al., 2012, 2016a, 2017a) and isocyanide reactions (Shiri et al., 2016b, 2017b; Salehi and Shiri, 2019), we began our investigation with 2-chloroquinoline-3-carbaldehyde (1) and its two step reaction with two different isocyanides. In the presence of K2CO3, 2-chloroquinoline-3-carbaldehyde (1) and 4-toluenesulfonylmethyl isocyanide (TosMIC) (2) furnished 5-(2-chloroquinolin-3-yl)oxazole (3a). Several 5-(2-chloroquinolin-3-yl)oxazoles (3) were prepared under the same conditions. The reaction of quinoline 3a with cyclohexyl isocyanide 4a was selected as a model reaction in the presence of Pd(OAc)2, Ph3P, and Cs2CO3, in 1,4-dioxane with a few drops of H2O as solvent at 80 °C. Desired product 5a was obtained in 86% yield (Table 1). Solvent screening showed that DMSO is the best solvent (Table 1, entry 6). Other Pd sources such as Pd(PPh3)4 and PdCl2 did not improve the product yield, however, the best yield was obtained with 5 mol% of Pd(OAc)2 even without PPh3 (Table 1, entries 7–9). Without palladium, the reaction did not occur (Table 1, entry 10). Moreover, the effect of base is crucial for reaction completion. Hence, different bases were investigated, including K2CO3, NaOAc, (CH3)3OK, DABCO, and Et3N (Table 1, entries 14–18). In this survey, it was found that increasing the temperatures or the reaction time decreased the product yield.

TABLE 1
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Table 1. Optimization of the reaction condition for the synthesis of N-cyclohexyl-3-(oxazol-5-yl)quinoline-2-carboxamide 5a from 3a.

With the optimized reaction conditions in hand (Pd(OAc)2 (5 mol%), Cs2CO3 (1 equiv.), DMSO + H2O (9:1), 80°C), the generality of the reaction was explored (Table 2). A range of quinolines 3 bearing electron-donating groups, such as Me, and OMe and electron-withdrawing groups, such as Cl and benzo, reacted with cyclohexyl isocyanide and n-butylisocyanide to afford the corresponding 3-(oxazol-5-yl)quinoline-2-carboxamides 5a-f in 70%-94% yields (Table 2). Moreover, the bulky tert-butyl isocyanide smoothly participated in this reaction to furnish 5g and 5h in 67 and 76% yield, respectively. The yield with 1,1,3,3-tetramethylbutyl isocyanide was too low to allow its isolation and characterization.

TABLE 2
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Table 2. Synthesis of various derivatives of 5a-5ha.

The scope of the reaction was explored using tosylmethyl isocyanide (TosMIC) 1 as another isocyanide source. Surprisingly, the reaction of 3a with TosMIC under the optimized conditions afforded 5-(2-tosylquinolin-3-yl)oxazole (6a) (Scheme 1).

SCHEME 1
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Scheme 1. The reaction of TosMIC with 3a.

Although the reaction proceeded well without a palladium source, the presence of base is crucial. Among the bases Cs2CO3, K2CO3, NaOAc, t-BuOK, and DABCO, Cs2CO3 gave the best results.

Encouraged by the tosylation results with TosMIC, we explored extending the reaction to tandem oxazole formation as well as tosylation of 2-chloroquinoline-3-carbaldehyde. Subjecting 2-chloroquinoline-3-carbaldehyde and TosMIC to the standard reaction conditions yielded 5-(2-tosylquinolin-3-yl)oxazole (6a) in 83% yield after 8 h (Scheme 2). Notably, sulfones are present in different bioactive compounds (Metzner and Thuillier, 1994; Fang et al., 2016); however, well-known sulfonylating agents include sulfonyl halides (Tocco et al., 2013; Zhang et al., 2015), sulfonyl hydrazides (Yuan et al., 2018; Zhang et al., 2018), and sodium sulfinate (Sun et al., 2017; Smith et al., 2018). A few studies used TosMIC as a sulfonyl precursor (Liu et al., 2014; Phanindrudu et al., 2016; Kadari et al., 2017). Furthermore, Bounar et al. reacted tosylmethyl isocyanide (TosMIC) with propargylic alcohols in the presence of silver acetate to efficiently yield (E)-vinyl sulfones (Bounar et al., 2015); this is the only study in which TosMIC plays a dual role as both an amide and a sulfonyl source.

SCHEME 2
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Scheme 2. One-pot synthesis of 5-(6-methyl-2-tosylquinolin-3-yl)oxazole 6a.

The above cascade oxazole formation and sulfonylation strategy could be extended to other 2-chloroquinoline-3-carbaldehyde derivatives (Figure 2). A methyl group was tolerated on positions 6 and 8 of 2 to afford 6b and 6c, respectively, in 82 and 62% yields. Furthermore, quinoline 2d reacted with TosMIC, affording 6d in good yield. Product 6e, existing an alternative decoration of the quinoline ring, was obtained in 85% yield.

FIGURE 2
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Figure 2. 5-(2-Tosylquinolin-3-yl)oxazole 6.

Our proposed mechanism for the tosylation of quinoline involved in situ Ts generation by decomposition of p-toluenesulfonylmethyl-isocyanide 1 in the presence of base with subsequent aromatic nucleophilic substitution to form 2-sulfonyl quinoline 6. Although application of TosMIC as a sulfonyl source was reported by Liu et al. for synthesizing sulfonyl benzoheteroles, the sulfonation mechanism involved aliphatic nucleophilic substitution (Liu et al., 2014).

Conclusion

In summary, we have developed a synthesis of 5-(2-chloroquinolin-3-yl)oxazole via a van Leusen procedure from 2-chloroquinoline-3-carbaldehydes and TosMIC, which were efficiently subjected to Pd-catalyzed amidation with isocyanides to form 3-(oxazol-5-yl)quinoline-2-carboxamides. The synthesis of 5-(2-tosylquinolin-3-yl)oxazole via a Cs2CO3-mediated domino process starting from 2-chloroquinoline-3-carbaldehydes with TosMIC was also demonstrated.

Author Contributions

ZM, ZT, and SF synthesized all of the compounds with the help of ZY. MS supervised this work and wrote the paper with the help of ZY.

Conflict of Interest Statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Acknowledgments

We are thankful to Alzahra University and the Iran National Science Foundation (INSF) for the financial support.

Supplementary Material

The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fchem.2019.00433/full#supplementary-material

Supplementary Data Sheet 1. Isocyanide reactions toward the synthesis of 3-(Oxazol-5-yl)quinoline-2-carboxamides and 5-(2-Tosylquinolin-3-yl)oxazole.

References

Åkerbladh, L., Schembri, L. S., Larhed, M., and Odell, L. R. (2017). Palladium(0)-catalyzed carbonylative one-pot synthesis of N-acylguanidines. J. Org. Chem 82, 12520–12529. doi: 10.1021/acs.joc.7b02294

PubMed Abstract | CrossRef Full Text | Google Scholar

Bode, J. W. (2006). Emerging methods in amide- and peptide-bond formation. Curr. Opin. Drug Discov. Devel. 9, 765–775. doi: 10.1002/chin.200721229

PubMed Abstract | CrossRef Full Text | Google Scholar

Bounar, H., Liu, Z., Zhang, L., Guan, X., Yang, Z., Liao, P., et al. (2015). Silver-catalyzed cascade reaction of tosylmethyl isocyanide (TosMIC) with propargylic alcohols to (E)-vinyl sulfones: dual roles of TosMIC. Org. Biomol. Chem. 13, 8723–8728. doi: 10.1039/C5OB01129A

PubMed Abstract | CrossRef Full Text | Google Scholar

Chaudhary, A., Sharma, P. P., Bhardwaj, G., Jain, V., Bharatam, P. V., Shrivastav, B., et al. (2013). Synthesis, biological evaluation, and molecular modeling studies of novel heterocyclic compounds as anti-proliferative agents. Med. Chem. Res. 22, 5654–5669. doi: 10.1007/s00044-013-0556-x

CrossRef Full Text | Google Scholar

Davyt, D., and Serra, G. (2010). Thiazole and oxazole alkaloids: isolation and synthesis. Mar. Drugs 8, 2755–2780. doi: 10.3390/md8112755

PubMed Abstract | CrossRef Full Text | Google Scholar

Domling, A. (2006). Recent developments in isocyanide based multicomponent reactions in applied chemistry. Chem. Rev. 106, 17–89. doi: 10.1021/cr0505728

PubMed Abstract | CrossRef Full Text | Google Scholar

Domling, A., and Ugi, I. (2000). Multicomponent eeactions with isocyanides. Angew. Chem. Int. Ed 39, 3168–3210. doi: 10.1002/1521-3773(20000915)39:18<3168::AID-ANIE3168>3.0.CO;2-U

PubMed Abstract | CrossRef Full Text

Fang, Y., Luo, Z., and Xu, X. (2016). Recent advances in the synthesis of vinyl sulfones. RSC Adv. 6, 59661–59676. doi: 10.1039/c6ra10731a

CrossRef Full Text | Google Scholar

Guan, Z.-R., Liu, Z.-M., and Ding, M. W. (2018). New efficient synthesis of 1H-imidazo-[4,5-c]quinolines by a sequential Van Leusen/Staudinger/aza-Wittig/carbodiimide-mediated cyclization. Tetrahedron 74, 7186–7192. doi: 10.1016/j.tet.2018.10.052

CrossRef Full Text | Google Scholar

Hranjec, M., Horak, E., Babic, D., Plavljanin, S., Srdovic, Z., Steinberg, I. M., et al. (2017). Fluorescent benzimidazo[1,2-a]quinolines: synthesis, spectroscopic and computational studies of protonation equilibria and metal ion sensitivity. N. J. Chem. 41, 358–371. doi: 10.1039/c6nj02268e

CrossRef Full Text | Google Scholar

Ishida, K., Nakagawa, H., and Murakami, M. (2000). Microcyclamide, a cytotoxic cyclic hexapeptide from the Cyanobacterium microcystis aeruginosa. J. Nat. Prod 63, 1315–1317. doi: 10.1021/np000159p

PubMed Abstract | CrossRef Full Text | Google Scholar

Jiang, H., Liu, B., Li, Y., Wang, A., and Huang, H. (2011). Synthesis of Amides via palladium-catalyzed amidation of aryl halides. Org. Lett. 13, 1028–1031. doi: 10.1021/ol103081y

PubMed Abstract | CrossRef Full Text | Google Scholar

Kadari, L., Palakodety, R. K., and Yallapragada, L. P. (2017). Electrochemical decarboxylative sulfonylation of cinnamic acids with aromatic sulfonylhydrazides to vinyl sulfones. Org. Lett. 19, 2580–9661. doi: 10.1021/acs.joc.7b01741

CrossRef Full Text

Linington, R. G., González, J., Ureña, L., Romero, L. I., Ortega-Barría, E., and Gerwick, W. H. (2007). Venturamides, A and B: antimalarial constituents of the panamanian marine cyanobacterium Oscillatoria sp. J. Nat. Prod. 70, 397–401. doi: 10.1021/np0605790

PubMed Abstract | CrossRef Full Text | Google Scholar

Liu, J., Liu, Z., Liao, P., and Bi, X. (2014). Modular synthesis of sulfonyl benzoheteroles by silver-catalyzed heteroaromatization of propargylic alcohols with p-toluenesulfonylmethyl isocyanide (TosMIC): dual roles of TosMIC. Org. Lett. 16, 6204–6207. doi: 10.1021/ol5031316

PubMed Abstract | CrossRef Full Text | Google Scholar

Marco-Contelles, J., Perez-Mayoral, E., Samadi, A., Carreiras, M. D., and Soriano, E. (2009). Recent advances in the Friedländer reaction. Chem. Rev. 109, 2652–2671. doi: 10.1021/cr800482c

PubMed Abstract | CrossRef Full Text | Google Scholar

Metzner, P., and Thuillier, A. (1994). Sulfur Reagents in Organic Synthesis. Best synthetic methods. eds A. R. Katritzky, O. Meth-Cohn, and C. W. Rees (London: Academic Press).

Google Scholar

Michael, J. P. (2002). Quinoline, quinazoline and acridone alkaloids. Nat. Prod. Rep. 19, 742–760. doi: 10.1039/B104971M

PubMed Abstract | CrossRef Full Text | Google Scholar

Montalbetti, C. A. G. N., and Falque, V. (2005). Amide bond formation and peptide coupling. Tetrahedron. 61, 10827–10852. doi: 10.1016/j.tet.2005.08.031

CrossRef Full Text | Google Scholar

Nainwal, L. M., Tasneem, S., Akhtar, W., Verma, G., Khan, M. F., Parvez, S., et al. (2019). Green recipes to quinoline: a review. Eur. J. Med. Chem. 164, 121–170. doi: 10.1016/j.ejmech.2018.11.026

PubMed Abstract | CrossRef Full Text | Google Scholar

Pathare, R. S., Sharma, S., Elagandhula, S., Saini, V., Sawant, D. M., Yadav, M., et al. (2016). Application of isocyanides as amide surrogates in the synthesis of diverse isoindolin-1-one derivatives by a palladium-catalyzed tandem carboxamidation/hydroamidation reaction. Eur. J. Org. Chem. 2016, 5579–5587. doi: 10.1002/ejoc.201600999

CrossRef Full Text | Google Scholar

Phanindrudu, M., Tiwari, D. K., Sridhar, B., Likhar, P. R., and Tiwari, D. K. (2016). Magnetically separable nano-copper catalyzed unprecedented stereoselective synthesis of E-vinyl sulfones from tosylmethyl isocyanide and alkynes: TosMIC as a source of the sulfonyl group. Org. Chem. Front. 3, 795–798. doi: 10.1039/C6QO00063K

CrossRef Full Text | Google Scholar

Prajapati, S. M., Patel, K. D., Vekariya, R. H., Panchal, S. N., and Patel, H. D. (2014). Recent advances in the synthesis of quinolines: a review. Rsc Adv. 4, 24463–24476. doi: 10.1039/c4ra01814a

CrossRef Full Text | Google Scholar

Raveh, A., Moshe, S., Evron, Z., Flescher, E., and Carmeli, S. (2010). Novel thiazole and oxazole containing cyclic hexapeptides from a waterbloom of the Cyanobacterium microcystis sp. Tetrahedron 66, 2705–2712. doi: 10.1016/j.tet.2010.02.008

CrossRef Full Text | Google Scholar

Rönn, R., Lampa, A., Peterson, S. D., Gossas, T., Åkerblom, E., Danielson, U. H., et al. (2008). Hepatitis C virus NS3 protease inhibitors comprising a novel aromatic P1 moiety. Bioorg. Med. Chem. 16, 2955–2967. doi: 10.1016/j.bmc.2007.12.041

PubMed Abstract | CrossRef Full Text | Google Scholar

Salehi, P., and Shiri, M. (2019). Palladium-catalyzed regioselective synthesis of 3-(hetero)arylpropynamides from gem-dibromoalkenes and isocyanides. Adv. Synth. Catal. 361, 118–125. doi: 10.1002/adsc.201800963

CrossRef Full Text | Google Scholar

Sharma, R., Kour, P., and Kumar, A. (2018). A review on transition-metal mediated synthesis of quinolines. J. Chem. Sci. 130:73. doi: 10.1007/s12039-018-1466-8

CrossRef Full Text | Google Scholar

Shiri, M., Faghihi, Z., Oskouei, H. A., Heravi, M. M., Fazelzadeh, S., and Notash, B. (2016a). The synthesis of iminothiophenone-fused quinolines and evaluation of their serendipitous reactions. RSC Adv. 6:92235. doi: 10.1039/c6ra11469e

CrossRef Full Text | Google Scholar

Shiri, M., Heydari, M., and Zadsirjan, V. (2017b). Efficient synthesis of novel functionalized pyrazolo-pyranoquinoline and tetrahydrodibenzo-[1,8]naphthyridinone derivatives. Tetrahedron 73,2116–2122. doi: 10.1016/j.tet.2017.02.064

CrossRef Full Text | Google Scholar

Shiri, M., Pourabed, R., Zadsirjan, V., and Sodagar, E. (2016b). Highly selective organocatalytic three-component reaction of 2-chloroquinoline-3-carbaldehydes, 6-aminouracils, and cyclic methylene active compounds. Tetrahedron Lett. 57, 5435–5438. doi: 10.1016/j.tetlet.2016.10.057

CrossRef Full Text | Google Scholar

Shiri, M., Ranjbar, M., Yasaei, Z., Zamanian, F., and Notash, B. (2017a). Palladium-catalyzed tandem reaction of 2-chloroquinoline-3-carbaldehydes and isocyanides. Org. Biomol. Chem. 15:10073. doi: 10.1039/c7ob02043k

PubMed Abstract | CrossRef Full Text | Google Scholar

Shiri, M., Zolfigol, M. A., Kruger, H. G., and Tanbakouchian, Z. (2011). Friedlander annulation in the synthesis of azaheterocyclic compounds. Adv. Heterocycl. Chem. 185, 139–227. doi: 10.1016/B978-0-12-385464-3.00002-9

CrossRef Full Text | Google Scholar

Shiri, M., Zolfigol, M. A., Pirveysian, M., Ayazi-Nasrabadi, R., Kruger, H. G., Naicker, T., et al. (2012). A new and facile access to the 2-(indol-3-yl)-3-nitriloquinolines based on Friedlander annulations. Tetrahedron 68, 6059–6064. doi: 10.1016/j.tet.2012.05.006

CrossRef Full Text | Google Scholar

Smith, J. D., Ansari, T. N., Andersson, M. P., Yadagiri, D., Ibrahim, F., Liang, S., et al. (2018). Micelle-enabled clean and selective sulfonylation of polyfluoroarenes in water under mild conditions. Green Chem. 20, 1784–1790. doi: 10.1039/C7GC03514D

CrossRef Full Text | Google Scholar

Sun, Y., Abdukader, A., Lu, D., Zhang, H., and Liu, C. (2017). Synthesis of (E)-β-iodo vinylsulfones via iodine-promoted iodosulfonylation of alkynes with sodium sulfinates in an aqueous medium at room temperature. Green Chem. 19, 1255–1258. doi: 10.1039/C6GC03387C

CrossRef Full Text | Google Scholar

Tocco, G., Begala, M., Esposito, F., Caboni, P., Cannas, V., and Tramontano, E. (2013). ZnO-mediated regioselective C-arylsulfonylation of indoles: a facile solvent-free synthesis of 2- and 3-sulfonylindoles and preliminary evaluation of their activity against drug-resistant mutant HIV-1 reverse transcriptases (RTs). Tetrahedron Lett. 54, 6237–6241. doi: 10.1016/j.tetlet.2013.09.017

CrossRef Full Text | Google Scholar

Tyagi, V., Khan, S., Giri, A., Gauniyal, H. M., Sridhar, B., and Chauhan, P. M. S. (2012). A ligand-free Pd-catalyzed cascade reaction: an access to the highly diverse isoquinolin-1(2H)-one derivatives via isocyanide and Ugi-MCR synthesized amide precursors. Org. Lett. 14, 3126–3129. doi: 10.1021/ol301131s

PubMed Abstract | CrossRef Full Text | Google Scholar

Ulijn, R. V., Moore, B. D., Janssen, A. E. M., and Halling, P. J. (2002). A single aqueous reference equilibrium constant for amide synthesis–hydrolysis. J. Chem. Soc. Perkin Trans. 2 1024–1028. doi: 10.1039/B108041E

CrossRef Full Text | Google Scholar

Vlaar, T., Ruijter, E., Znabet, A., Janssen, E., de Kanter, F. J. J., Maes, B. U. W., et al. (2011). Palladium-catalyzed synthesis of 4-aminophthalazin-1(2H)-ones by isocyanide insertion. Org. Lett. 13, 6496–6499. doi: 10.1021/ol202784d

PubMed Abstract | CrossRef Full Text | Google Scholar

Wang, L., Woods, K. W., Li, Q., Barr, K. J., McCroskey, R. W., Hannick, S. M., et al. (2002). Potent, orally active heterocycle-based combretastatin A-4 cnalogues: synthesis, structure–activity relationship, pharmacokinetics, and in vivo antitumor activity evaluation. J. Med. Chem. 45, 1697–1711. doi: 10.1021/jm010523x

PubMed Abstract | CrossRef Full Text | Google Scholar

Yavari, I., Ghazanfarpour-Darjani, M., and Bayat, M. J. (2014). Synthesis of amides via copper-catalyzed amidation of aryl halides using isocyanides. Tetrahedron Lett. 55, 4981–4982. doi: 10.1016/j.tetlet.2014.05.032

CrossRef Full Text | Google Scholar

Yu, L.-L., Li, Z. -Y., Peng, C. -S., Li, Z. -Y., and Guo, Y. -W. (2009). Neobacillamide, A., a novel thiazole-containing alkaloid from the marine bacterium Bacillus vallismortis C89, associated with south China sea sponge Dysidea avara. Helv. Chim. Acta 92, 607–612. doi: 10.1002/hlca.200800349

CrossRef Full Text | Google Scholar

Yuan, Y., Yu, Y., Qiao, J., Liu, P., Yu, B., Zhang, W., et al. (2018). Exogenous-oxidant-free electrochemical oxidative C–H sulfonylation of arenes/heteroarenes with hydrogen evolution. Chem. Commun. 54, 11471–11474. doi: 10.1039/C8CC06451B

PubMed Abstract | CrossRef Full Text | Google Scholar

Zhang, D., Cui, X., Zhang, Q., and Wu, Y. (2015). Pd-Catalyzed direct C–H bond sulfonylation of azobenzenes with arylsulfonyl chlorides. J. Org. Chem. 80, 1517–1522. doi: 10.1021/jo502451k

PubMed Abstract | CrossRef Full Text | Google Scholar

Zhang, J., Wang, Z., Chen, L., Liu, Y., Liu, P., and Dai, B. (2018). The fast and efficient KI/H2O2 mediated 2- sulfonylation of indoles and N-methylpyrrole in water. RSC Adv. 8, 41651–41656. doi: 10.1039/c8ra09367a

CrossRef Full Text | Google Scholar

Keywords: palladium acetate, carboxamidation, isocynides, sulfonylation, TosMIC

Citation: Yasaei Z, Mohammadpour Z, Shiri M, Tanbakouchian Z and Fazelzadeh S (2019) Isocyanide Reactions Toward the Synthesis of 3-(Oxazol-5-yl)Quinoline-2-Carboxamides and 5-(2-Tosylquinolin-3-yl)Oxazole. Front. Chem. 7:433. doi: 10.3389/fchem.2019.00433

Received: 03 January 2019; Accepted: 28 May 2019;
Published: 14 June 2019.

Edited by:

Jonathan G. Rudick, Stony Brook University, United States

Reviewed by:

Steven Ballet, Vrije University Brussel, Belgium
Zhong-zhu Chen, Chongqing University of Arts and Sciences, China

Copyright © 2019 Yasaei, Mohammadpour, Shiri, Tanbakouchian and Fazelzadeh. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Morteza Shiri, mshiri@alzahra.ac.ir

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