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Article

Green and Highly Efficient Synthesis of 2-Arylbenzothiazoles Using Glycerol without Catalyst at Ambient Temperature

by
Kamal Usef Sadek
1,*,
Ramadan Ahmed Mekheimer
1,2,
Afaf Mohamed Abdel Hameed
1,
Fatma Elnahas
1 and
Mohamed Hilmy Elnagdi
3
1
Chemistry Department, Faculty of Science, El-Minia University, El-Minia 61519, Egypt
2
Chemistry Department, Faculty of Science for Girls, King Abdulaziz University, P.O. Box 50918, Jeddah 21533, Saudi Arabia
3
Chemistry Department, Faculty of Science, Kuwait University, P.O. Box 5969, Safat 13060, Kuwait
*
Author to whom correspondence should be addressed.
Molecules 2012, 17(5), 6011-6019; https://doi.org/10.3390/molecules17056011
Submission received: 27 March 2012 / Revised: 9 May 2012 / Accepted: 10 May 2012 / Published: 18 May 2012
(This article belongs to the Section Organic Chemistry)
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Abstract

:
A one-pot and clean synthesis of 2-arylbenzothiazoles via the ambient temperature reaction of 2-aminothiophenols and aromatic aldehydes without catalyst in glycerol as a green solvent has been reported.

Graphical Abstract

1. Introduction

With technological and scientific advancement comes cost, and with respect to this issue, the most important cost to be dealt with is the impact of these technologies on our environment [1]. Most organic reactions occur in a liquid phase. Taking into account the impact of chemical processes on the environment, the search for green solvents has become a great challenge in organic synthesis, as solvents are responsible for a large part of the waste and pollution generated by chemical processes, a key factor in any green chemical process is solvent selection [2].
Glycerol is a non-toxic, biodegradable and recyclable liquid that is highly inert, stable and also dissolves organic compounds that are poorly miscible in water. It combines the advantages of water (low toxicity, low price, wide availability) and ionic liquids (highly boiling point, low vapor pressure) [3]. These advantages make it ideal for use as a sustainable solvent in organic synthesis.
2-Arylbenzothiazoles can be found in a variety of natural products as well as a number of biologically active compounds [4]. They are a class of potent and selective antitumor agents which exhibit nanomolar inhibitory activity against a range of human breast, colon and renal cell lines in vitro [5]. In addition, they possess significant utility as imaging agents for β-amyloid, antitubercullotic, chemiluminescent agents, calcium channel antagonists, antiparasitics and photosensitizers [6,7,8,9,10].
To date, two common strategies have been developed used for the synthesis of 2-arylbenzothiazoles. The first approach is through arylation of benzothiazole with aryl bromides catalyzed by Pd(OAc)2, Cs2CO3 and CuBr with P(t-Bu)3 as a ligand at 150 °C in a sealed tube [11], or Suzuki biaryl coupling of 2-bromothiazoles with arylboronic acids [12]. The second method is via condensation of 2-aminothiophenols with substituted nitriles, carboxylic acids, aryl chlorides, esters or aldehydes [13]. A number of catalysts such as (PmIm)Br [14], I2 [15], ZrOCl2•8H2O [16], TMSCl [17], PCC [18], CAN [19], molecular oxygen [20], H2O2 [21], MnO2 [22], Baker’s yeast [23], animal bone meal [24], electrooxidation [25], Na2S2O5 in refluxing DMF [26] have been used to perform the cyclization step. Recently, some green approaches for the preparation of 2-arylbenzothiazoles based on the direct condensation of 2-aminothiophenols with aromatic aldehydes have been reported. They involve the use of PTSA either in water at 70 °C or PEG, 200/400 under microwave heating [27,28], Cu(OAc)2/MCM41 supported catalyst under ultrasound irradiation [29], NIBTS at ambient temperature under solvent free conditions [30], Dowex 50W reusable catalyst in water at 70 °C [31], TCCA in MeTHF at ambient temperature [32], heating in water at 110 °C [33], 2,4,6-trichloro-1,3,5-triazine under mild conditions [34], H2SO4/SiO2 as a reusable catalyst at room temperature [35] or sulfamic acid as a reusable catalyst in water at room temperature [36]. Although, these methods each have specific merits, they suffering from some drawbacks such as high temperature conditions, long reaction times and sometimes low yields. In addition, the catalysts employed in most of these cyclization steps are not always inexpensive or eco-friendly, and consequently, serious environmental pollution often results when the catalysts contaminate the environment. Since glycerol is able to dissolve organic compounds that are poorly miscible in water, its use as a green solvent without catalyst would overcome such drawbacks. Also, conducting the reaction at ambient temperature will increase the energy efficiency of the reaction. Very recently, a one-step synthesis of 2-arylbenzothiazoles from the reaction of gem-dibromomethylarenes with 2-aminothiophenol employing t-BuOK and a catalytic amount of iodine in pyridine at reflux temperature has been reported [37]. In 2012, Cheng and co-workers have described another approach to 2-arylbenzothiazoles via Jacobson’s cyclization of thiobenzanilides catalyzed by aerobic visible light, but this route requires a multistep reaction sequence [38]. In this regard, employing a benign solvent under catalyst free conditions for the synthesis of the target molecules will be of great interest in the area of green chemistry.
In continuation of our work aiming at development of efficient, simple and green technologies for the synthesis of heterocycles [39,40,41], we reported herein a one-pot synthesis of 2-arylbenzothiazoles from the ambient temperature reaction of 2-aminothiophenols 1 with aromatic aldehydes 2 in glycerol under catalyst free conditions.

2. Results and Discussion

With the initial aim of optimising the experimental conditions, we explored the reaction of 2-aminothiophenol (1a) and benzaldehyde (2a) using glycerol as a solvent to afford the desired 2-phenyl-1,3-benzothiazole (4a) (Scheme 1). Thus, when a mixture of 1a (0.1 mol) and 2a (0.1 mol) in glycerol (10 mL) was stirred at room temperature, it was observed that reactants were recovered almost unchanged after a long period of time. The reaction promoted by just heating the reaction mixture until the reactants were dissolved and then left at room temperature for 30 min afforded 4a in excellent yield. The structure of compound 4a could be established on the basis of analytical and spectral data and comparison with authentic specimen prepared via an alternative route [18]. Similarly, compounds 1a–c reacted with 2b–k, under the same reaction conditions, to afford 4b–k in excellent yields.
In order to study the effect of solvent on the rate of the reaction we carried out the same reaction in different solvents, such as H2O, acetone and CHCl3, under the same reaction conditions, and the reactants were recovered almost unchanged. Next, we studied the effect of aromatic aldehyde substituents on the reaction rate and the overall yield. With both electron withdrawing and electron donating groups, the reaction proceeds smoothly, with a slight increase in the yield when the aryl substituent bore an electron withdrawing group. We also studied the generality and applicability of such protocol via examining the reaction of substituted 2-aminothiophenols bearing both electron donating and electron withdrawing groups. In both cases, the reaction proceeds smoothly with good yields. Although until now the reasons behind the promoting effect of glycerol are still unclear, a mechanism to account for the formation of 4a–k is postulated in Scheme 2.
The highly solving action of glycerol on the reactants makes them readily available to interact and the carbonyl carbon of the aldehyde will be activated because of the intermolecular hydrogen bonding with the hydroxyl groups of glycerol. In addition, the formed intermediates could be stabilized by several types of complexations and hydrogen bonding with the hydroxyl groups of glycerol. This was followed by cyclization to form the corresponding thiazoline intermediate 3 which, on dehydrogenation, via aerial oxidation, is converted to the thiazole 4 which will enjoy the aromaticity (i.e., stabilization) of the benzothiazole ring system. Conducting the reaction of 1a with 2a in the absence of air resulted in a sluggish reaction inconvenient for complete product formation even after a longer reaction time. It is worth mentioning that strong oxidants or more interestingly catalytic aerobic oxidation involving oxygen as a terminal oxidant have received considerable attention in the synthesis of benzothiazoles [21]. The advantage of our protocol is the use of only atmospheric air as the oxidant at ambient temperature. However, we cannot totally rule out that the presence of trace amount of acidic and basic derivatives in glycerol can act as possible catalysts.

3. Experimental

3.1. General

Melting points were determined on a Gallenkamp melting point apparatus and are uncorrected. 2-Aminothiophenol (1a–c) and aldehydes 2a–k were commercially available. Infrared spectra were measured with a Schimadzu Model 470 spectrophotometer. The 1H- and 13C-NMR spectra were recorded on a Bruker AM 400 spectrometer (at 400 MHz for 1H-NMR and 100 MHz for 13C-NMR) with DMSO-d6 as solvent and TMS as internal reference, chemical shifts are expressed as δ ppm. Mass spectra were measured on a GCMS-QP1000EX mass spectrometer. Analytical data were determined on the Microanalytical Data Unit at Kuwait University. Analytical TLC was performed with a silica gel plates using silica gel 60 PF254 (Merck).

3.2. Synthesis of 2-Arylbenzothiazoles 4a–k

A mixture of thiophenols 1a–c (1.25 g, 10 mmol) and the appropriate aldehyde 2 (10 mmol) in glycerol (10 mL) was heated until a clear solution was obtained and then left at room temperature for 0.5–5 h (TLC control). The reaction mixture was quenched with water and the resulting solid product was collected by filtration, dried and recrystallised from EtOH to afford compounds 4a–k.
2-Phenyl-1,3-benzothiazole (4a). Yield: 92%; reaction time 0.5 h; mp 112–113 °C (Lit. [18] 115–116); IR (KBr): ν = 3,060, 3,020, 1,609, 1,590 cm−1; 1H-NMR: δ = 8.17 (d, 1H), 8.12–8.07 (m, 3H), 7.59–7.50 (m, 4H), 7.45 (t, 1H) ppm; 13C-NMR: δ = 167.30, 153.56, 134.45, 132.85, 131.44, 129.42, 127.20, 126.68, 125.57, 122.90, 122.38 ppm; MS m/z (rel. int. %) 211 (M+, 100); Anal. Calcd. for C13H9NS (211.28): C, 73.90; H, 4.29; N, 6.63; S, 15.18. Found: C, 73.79; H, 4.19; N, 6.81; S, 14.98.
2-(4-Methoxyphenyl)-1,3-benzothiazole (4b). Yield 90%; reaction time 4h; mp 126–128 °C (Lit. [25] 119–120 °C); IR (KBr): ν = 3,100, 3,060, 1,605, 1,585 cm−1; 1H-NMR: δ = 8.12 (d, 1H), 8.1–8.0 (m, 3H), 7.53 (t, 1H), 7.45 (t, 1H), 7.13 (d, 2H), 3.85 (s, 3H) ppm; 13C-NMR: δ = 167.05, 153.67, 134.23, 128.88, 126.52, 125.52, 125.11, 122.47, 122.20, 114.75, 55.5 ppm; MS m/z (rel. int. %) 241 (M+, 100); Anal. Calcd. for C14H11NOS (241.31): C, 69.68; H, 4.59; N, 5.80; S, 13.29. Found: C, 69.55; H, 4.52; N, 5.94; S, 13.18.
2-(3-Nitrophenyl)-1,3-benzothiazole (4c). Yield 92%; reaction time 2 h; mp 184–186 °C (Lit. [18] 181–183 °C); IR (KBr): ν = 3,080, 3,035, 1,612, 1,580 cm−1; 1H-NMR: δ = 8.84 (s, 1H), 8.44 (d, 1H), 8.41 (d, 1H), 8.24 (d, 1H), 8.16 (d, 1H), 7.88 (t, 1H), 7.60 (t, 1H), 7.54 (t, 1H) ppm; 13C-NMR: δ = 161.9, 157.5, 149.4, 142.8, 133.3, 130.7, 130.2, 126.5, 126.3, 122.5, 120.3, 119.5, 111.8 ppm; MS m/z (rel. int. %) 256.0 (M+, 100); Anal. Calcd. for C13H8N2O2S (256.28): C, 60.93; H, 3.15; N, 10.93; S, 12.51. Found: C, 60.86; H, 3.27; N, 11.02; S, 12.64.
2-(4-Chlorophenyl)-1,3-benzothiazole (4d). Yield 93%; reaction time 3 h; mp 116–118 °C (Lit. [25] 115–117 °C); IR (KBr): ν = 3,088, 3,030, 1,615, 1,590 cm−1; 1H-NMR: δ = 8.18 (d, 1H), 8.09 (d, 1H), 7.68 (d, 2H), 7.57 (d, 2H), 7.48 (m, 2H) ppm; Anal. Calcd. for C13H8ClNS (245.73): C, 63.54; H, 3.28; Cl, 14.43; N, 5.70; S, 13.05. Found: C, 63.47; H, 3.39; Cl, 14.58; N, 5.76; S, 12.87.
2-(3,4-Dimethoxyphenyl)-1,3-benzothiazole (4e). Yield 83%; reaction time 4 h; mp 130–132 °C (Lit. [19] 130–132 °C); IR (KBr): ν = 3,078, 3,052, 2,962, 2,835, 1,600 cm−1; 1H-NMR: δ = 8.10 (d, 1H), 8.09–8.02 (m, 1H), 7.66–7.60 (m, 2H), 7.53 (t, 1H), 7.41 (t, 1H), 7.12 (d, 1H), 3.88 (s, 3H), 3.85 (s, 3H) ppm; MS m/z (rel. int. %) 271 (M+, 100); Anal. Calcd. for C15H13NO2S (271.33): C, 66.40; H, 4.83; N, 5.16; S, 11.82. Found: C, 66.36; H, 4.73; N, 5.25; S, 11.69.
2-(4-Nitrophenyl)-1,3-benzothiazole (4f). Yield 94%; reaction time 2 h; mp 224–225 °C (Lit. [25] 224–226 °C); IR (KBr): ν = 3,082, 3,035, 1,615, 1,580 cm−1; 1H-NMR: δ = 8.32 (d, 2H), 8.21 (d, 1H), 8.10 (d, 2H), 8.01 (d, 1H), 7.53–7.44 (m, 2H) ppm; MS m/z (rel. int. %) 256.0 (M+, 100); Anal. Calcd. for C13H8N2O2S (256.28): C, 60.93; H, 3.15; N, 10.93; S, 12.51. Found: C, 60.88; H, 3.25; N, 11.05; S, 12.64.
2-(3,4,5-Timethoxyphenyl)-1,3-benzothiazole (4g). Yield 82%; reaction time 5 h; mp 130–131 °C; IR (KBr): ν = 3,082, 3,055, 2,965, 2,833, 1,600 cm−1; 1H-NMR: δ = 8.09–8.02 (m, 1H), 7.66–7.60 (m, 2H), 7.53 (t, 1H), 7.41 (s, 1H), 7.22 (s, 1H), 3.89 (s, 3H), 3.87 (s, 3H), 3.84 (s, 3H) ppm; Anal. Calcd. for C16H15NO3S (301.36): C, 63.77; H, 5.02; N, 4.65; S, 10.64. Found: C, 63.66; H, 5.03; N, 4.56; S, 10.72.
2-(2-Hydroxyphenyl)-1,3-benzothiazole (4h). Yield 80%; reaction time 5 h; mp 123–124 °C; IR (KBr): ν = 3,450, 3,080, 3,042, 1,625 cm−1; 1H-NMR: δ = 8.21 (d, 1H), 8.16–8.01 (m, 3H), 7.62 (t, 1H), 7.53 (t, 1H), 7.07 (d, 2H) ppm; Anal. Calcd. for C13H9NOS (227.28): C, 68.70; H, 3.99; N, 6.16; S, 14.11. Found: C, 68.73; H, 4.01; N, 6.21; S, 14.24.
2-Thienyl-1,3-benzothiazole (4i). Yield 81%; reaction time 5 h; mp 97–99 °C (Lit. [19] 97–99 °C); IR (KBr): ν = 3,083, 3,040, 1,630 cm−1; 1H-NMR: δ = 8.22 (d, 1H), 8.14 (d, 1H), 7.72 (d, 1H), 7.69 (d, 1H), 7.63–7.54 (m, 2H), 7.31 (t, 1H) ppm; MS m/z (rel. int. %) 217.0 (M+, 100); Anal. Calcd. for C11H7NS2 (217.31): C, 60.80; H, 3.25; N, 6.45; S, 29.51. Found: C, 60.71; H, 3.19; N, 6.62; S, 29.33.
6-Chloro-2-(4-methoxyphenyl)benzothiazole (4j). Yield 88%; reaction time 4 h; mp 137–138 °C (Lit. [28] 136–138 °C); IR (KBr): ν = 3,090, 3,060, 1,610, 1,590 cm−1; 1H-NMR: δ = 8.19 (s, 1H), 8.02 (d, 2H), 7.89 (d, 1H), 7.68 (d, 1H), 7.08 (d, 2H), 3.83 (s, 3H) ppm; Anal. Calcd. for C14H10ClNOS (275.75): C, 60.98; H, 3.66; N, 5.08. Found: C, 60.88; H, 3.96; N, 5.22.
6-Methoxy-2-(4-nitrophenyl)benzothiazole (4k). Yield 80%; reaction time 5 h; mp 156–157 °C (lit. [28] 156–158 °C); IR (KBr): ν = 3,080, 3,035, 1,620, 1,580 cm−1; 1H-NMR: δ = 8.23 (d, 2H), 8.08 (d, 2H), 7.73 (s, 1H), 7.58 (d, 1H), 7.19 (d, 1H), 3.83 (s, 3H) ppm; 13C-NMR: δ = 170.0, 156.7, 149.6, 147.9, 146.7, 136.8, 128.4, 124.6, 122.8, 114.7, 104.9, 55.8 ppm; MS m/z (rel. int. %) 286 (M+, 100); Anal. Calcd. for C14H10N2O3S (286.31): C, 58.73; H, 3.52; N, 9.78 . Found: C, 58.66; H, 3.55; N, 9.66.

4. Conclusions

Glycerol has been employed for the first time as a benign solvent for the one-pot synthesis of 2-arylbenzothiazoles under catalyst free conditions and at ambient temperature. The procedure proved to be simple both in conducting the reaction and isolation of the products. The yields obtained are excellent and the products were recovered in pure form from the reaction mixture. To the best of our knowledge, it is one of the few reported one-pot syntheses of 2-arylbenzothiazoles, from the reaction of 2-aminothiophenol with aromatic aldehydes, at ambient temperature without catalyst.

References and Notes

  1. Anastas, P.T.; Warner, J.C. Green Chemistry: Theory and Practice; Oxford University Press: New York, NY, USA, 1998. [Google Scholar]
  2. Candeias, N.R.; Branco, L.C.; Gois, P.M.P.; Afonso, C.A.M.; Trindade, A.F. More Sustainable approaches for the synthesis of N-based heterocycles. Chem. Rev. 2009, 109, 2703–2802. [Google Scholar] [CrossRef] [PubMed]
  3. Gu, Y.; Jerome, F. Glycerol as a sustainable solvent for green chemistry. Green Chem. 2010, 12, 1127–1138. [Google Scholar] [CrossRef]
  4. Tasler, S.; Muller, O.; Wieber, T.; Herz, T.; Peyoraro, W.S.; Lang, M.; Krauss, R.; Totzke, F.; Zirrgiebel, U.; Ehlert, J.E.; et al. Substituted 2-arylbenzothiazoles as kinase inhibitors: Hit-to-lead optimization. Bioorg. Med. Chem. 2009, 19, 6728–6737. [Google Scholar] [CrossRef] [PubMed]
  5. Kashiyama, E.; Hutchinson, I.; Chua, M.S.; Stinson, S.F.; Phillipes, L.R.; Kaur, G.; Sausville, E.A.; Bradshaw, T.D.; Westwell, A.D.; Stevens, M.F. Antitumor benzothiazoles 8. Synthesis, metabolic and biological properties of the C- and N-oxidation products of antitumor 2-(4-aminophenyl)benzothiazole. J. Med. Chem. 1999, 42, 4172–4184. [Google Scholar] [CrossRef] [PubMed]
  6. Mathis, C.A.; Bacski, B.J.; Kajdasz, S.T.; McLellan, M.E.; Frosch, M.P.; Hyman, B.T.; Holt, D.P.; Wany, Y.; Huany, G.-F.; Debnath, M.L.; et al. A Lipophilic thioflavin-T. derivatives for positron emission tomography (PET) imagin of amyloid brain. Bioorg. Med. Chem. Lett. 2002, 12, 295–298. [Google Scholar] [CrossRef]
  7. Yamamoto, K.; Fujitta, M.; Tabashi, K.; Kawashima, Y.; Kato, E.; Oya, M.; Iso, T.; Iwao, J. Novel calcium antagonists. Synthesis and structure-activity relationship studies of benzothiazoline derivatives. J. Med. Chem. 1988, 31, 919–930. [Google Scholar] [CrossRef] [PubMed]
  8. Yoshida, H.; Nakao, R.; Nohta, H.; Yamaguchi, M. Chemiluminescent properties of some luminol-related compounds-part 3. Dyes Pigm. 2000, 47, 239–245. [Google Scholar] [CrossRef]
  9. Lee, B.C.; Jung, J.H.; Jeong, J.M.; Kim, S.E. Aromatic radioflurination and biological evaluation of 2-aryl-6-[18F]fluorobenzthiazoles as a potential positron emission tomography imaging probe for β-amyloid plakues. Bioorg. Med. Chem. 2011, 19, 2980–2990. [Google Scholar] [CrossRef] [PubMed]
  10. Xie, Y.; Deng, S.; Chen, Z.; Yan, S.; landry, D.W. Identification of small-molecule inhibitors of the AB-ABAD interaction. Bioorg. Med. Chem. Lett. 2006, 16, 4657–4660. [Google Scholar] [CrossRef] [PubMed]
  11. Alagille, D.; Baldwin, R.M.; Tamagnan, G.D. One-pot synthesis of 2-arylbenzothiazole (BTA) and benzoxazole precoursers for in vivo imaging of β-amyloid plaques. Tetrahedron Lett. 2005, 46, 1349–1351. [Google Scholar] [CrossRef]
  12. Majo, V.J.; Prabhakaran, J.; Mann, J.J.; Kumar, J.S.D. An efficient palladium catalyzed synthesis of 2-arylbenzothiazoles. Tetrahedron Lett. 2003, 44, 8535–8537. [Google Scholar] [CrossRef]
  13. Sharghi, H.; Asemani, O. Methansulfonic acid/SiO2 as an efficient combination for the synthesis of 2-substituted aromatic and aliphatic benzothiazoles from carboxylic acids. Synth. Commun. 2009, 39, 860–867. [Google Scholar] [CrossRef]
  14. Ranu, B.C.; Jana, R.; Dey, S. An efficient and green synthesis of 2-arylbenzothiazoles in an ionic liquid [PmIm]Br under microwave irradiation. Chem. Lett. 2004, 33, 274–275. [Google Scholar] [CrossRef]
  15. Li, Y.; Wang, Y.L.; Wang, J.Y. A simple iodine promoted synthesis of 2-substituted benzothiazoles by condensation of aldehydes with 2-aminothiophenol. Chem. Lett. 2006, 35, 460–461. [Google Scholar] [CrossRef]
  16. Moghadhan, F.M.; Ismaili, H.; Bardajee, C.R. Zirconium (IV) oxide chloride and anhydrous copper (II) sulfate mediated synthesis of 2-substituted benzothiazoles. Heteroatom Chem. 2006, 17, 136–141. [Google Scholar] [CrossRef]
  17. Robukhin, S.V.; Plaskon, A.S.; Volochnyuk, D.M.; Tolmachev, A.A. Synthesis of fused imidazoles and benzothiazoles from (hetero) aromatic ortho-diamines or ortho-aminothiophenols and aldehydes promoted by chlorotrimethylsilane. Synthesis 2006, 2006, 3715–3726. [Google Scholar] [CrossRef]
  18. Praveen, C.; Hemanthkumar, K.; Muralidharan, D.; Perumal, P.T. Oxidative cyclization of thiophenolic and phenolic Schiff’s bases promoted by PCC. A new oxidant for 2-substituted benzothiazoles and benzoxazoles. Tetrahedron 2008, 64, 2369–2374. [Google Scholar] [CrossRef]
  19. Al-Qalaf, F.; Mekheimer, R.A.; Sadek, K.U. Cerium (IV) ammonium nitrate (CAN) catalyzed one-pot synthesis of 2-arylbenzothiazoles. Molecules 2008, 13, 2908–2914. [Google Scholar] [CrossRef] [PubMed]
  20. Itoh, T.; Nagata, K.; Ishikawa, H.; Ohsawa, A. Synthesis of 2-arylbenzothiazoles and imidazoles using scandium triflate as a catalyst for both a ring closing and an oxidation step. Heterocycles 2004, 63, 2769–2783. [Google Scholar] [CrossRef]
  21. Bahrami, K.; Khodaei, M.M.; Naali, F. Mild and highly efficient method for the synthesis of imidazoles and 2-arylbenzothiazoles. J. Org. Chem. 2008, 73, 6835–6837. [Google Scholar] [CrossRef] [PubMed]
  22. Wilfred, C.D.; Taylor, R.J.K. Preparation of 2-substituted benzimidazoles and related heterocycles directly from activated alcohols using top methodology. Synlett 2004, 2004, 1628–1630. [Google Scholar] [CrossRef]
  23. Prutap, U.R.; Mali, J.R.; Jawale, D.V.; Mane, R.A. Baker’s yeast catalyzed synthesis of benzothiazoles in an organic medium. Tetrahedron Lett. 2009, 50, 1352–1354. [Google Scholar] [CrossRef]
  24. Riadi, Y.; Mamouni, R.; Azzelaou, R.; El Haddad, M.; Routier, S.; Guillaumet, G.; Lazar, S. An efficient and reusable heterogenious catalyst animal bone meal for the synthesis of benzimidazoles, benzoxazoles and benzothiazoles. Tetrahedron Lett. 2011, 52, 3492–3495. [Google Scholar] [CrossRef]
  25. Okimoto, M.; Yoshida, T.; Hoshi, M.; Hattori, K.; Komata, M.; Tomozawa, K.; Chiba, T. Electrooxidative cyclization of benzylideneaminothiophenols to the corresponding 2-arylbenzo-thiazoles. Heterocycles 2008, 75, 35–42. [Google Scholar] [CrossRef]
  26. Khan, K.M.; Rahim, F.; Halim, S.A.; Taha, M.; Khan, M.; Perveen, S.; Haq, Z.; Mesaik, M.A.; Choudhary, M.I. Synthesis of novel inhibitors of β-glucuronidase based on benzothiazole skeleton and study of their binding affinity by molecular docking. Bioorg. Med. Chem. 2011, 19, 4286–4294. [Google Scholar] [CrossRef] [PubMed]
  27. Azizi, N.; Amiri, A.K.; Baghi, R.; Bolourtchian, M.; Hashemi, M.M. PTSA catalyzed simple and green synthesis of benzothiazole derivatives in water. Monatsh. Chem. 2009, 140, 1471–1473. [Google Scholar] [CrossRef]
  28. Deligeorgiev, T.G.; Kaloyanova, S.; Vasilev, A.; Vaquero, J.J. Novel green procedure for the synthesis of 2-arylbenzothiazoles under microwave irradiation in PEG 200 or PEG 400. Phosphorus Sulfur Silicon Relat. Elem. 2010, 185, 2292–2302. [Google Scholar] [CrossRef]
  29. Sadjadi, S.; Sepehrian, H. Cu(OAc)2/MCM-41: An efficient and solid acid catalyst for synthesis of 2-arylbenzothiazoles under ultrasound irradiation. Ultrason. Sonochem. 2011, 18, 480–483. [Google Scholar] [CrossRef] [PubMed]
  30. Veisi, H.; Ghorbani-Vaghei, R.; Fraji, A.; Ozturk, T. Application of N,N′-diiodo-N,N′-1,2-ethandiylbis(p-toluene sulfonamide) as a new reagent for synthesis of 2-arylbenzimidazoles and 2-arylbenzothiazoles under solvent-free conditions. Chin. J. Chem. 2010, 28, 2249–2254. [Google Scholar] [CrossRef]
  31. Mukhopadhyay, C.; Datta, A. Water-promoted dowex 50W catalyzed highly efficient green protocol for 2-arylbenzothiazole formation. J. Heterocycl. Chem. 2009, 46, 91–95. [Google Scholar] [CrossRef]
  32. Xiao, H.-L.; Chen, J.-X.; Liu, M.-C.; Zhu, D.-J.; Ding, J.-C.; Wu, H.-Y. Trichloroisocyanuric acid (TCCA) as a mild and efficient catalyst for the synthesis of 2-arylbenzothiazoles. Chem. Lett. 2009, 38, 170–171. [Google Scholar] [CrossRef]
  33. Chakraborti, A.K.; Rudrawar, S.; Jadhav, K.B.; Kaur, G.; Chankeshwara, S.V. “On water” organic synthesis: A highly efficient and clean synthesis of 2-aryl/heteroaryl/styryl benzothiazoles and 2-alkyl/aryl alkyl benzothiazolines. Green Chem. 2007, 9, 1335–1340. [Google Scholar] [CrossRef]
  34. Maleki, B.; Azarifar, D.; Hojati, S.F.; Gholizadeh, M.; Veisi, H.; Salehabadi, H.; Khodaverdian Moghadam, M. Efficient 2,4,6-trichloro-1,3,5-triazine-catalyzed synthesis of 2-arylbenzothiazoles and bisbenzothiazoles by condensation of 2-aminithiophenol with aldehydes under mild conditions. J. Heterocycl. Chem. 2011, 48, 449–453. [Google Scholar] [CrossRef]
  35. Maleki, B.; Salehabadi, H.; Khodaverdian Moghaddam, M. Room-temperature synthesis of 2-arylbenzothiazoles using sulfuric acid immobilized on silica as a reusable catalyst under heterogeneous conditions. Acta Chim. Solv. 2010, 57, 741–745. [Google Scholar]
  36. Rostami, A.; Yari, A. Sulfamic acid as a recyclable and green catalyst for rapid and highly efficient synthesis of 2-arylbenzothiazols in water at room temperature. J. Iran. Chem. Soc. 2012. [Google Scholar] [CrossRef]
  37. Siddappa, C.; Kambappa, V.; Umashankara, M.; Rangappa, K.S. One-pot approach for the synthesis of 2-arylbenzothiazoles via a two-component coupling of gem-dibromomethylarenes and o-aminothiophenols. Tetrahedron Lett. 2011, 52, 5474–5477. [Google Scholar] [CrossRef]
  38. Cheng, Y.; Yang, J.; Qu, Y.; Li, P. Aerobic visible-light photoredox radical C-H functionalization: Catalytic synthesis of 2-substituted benzothiazoles. Org. Lett. 2012, 14, 98–101. [Google Scholar] [CrossRef] [PubMed]
  39. Mekheimer, R.A.; Abdel-Hameed, A.; Sadek, K.U. Solar thermochemical reactions: Four component synthesis of polyhydroquinoline derivatives induced by solar thermal energy. Green Chem. 2008, 10, 592–593. [Google Scholar] [CrossRef]
  40. Sadek, K.U.; Mekheimer, R.A.; Mohamed, T.M.; Moustafa, M.S.; Elnagdi, M.H. Regioselectivity in the multicomponent reaction of 5-aminopyrazoles, cyclic 1,3-diketones and dimethylformamide dimethylacetal under controlled microwave heating. Beilstein J. Org. Chem. 2012, 8, 18–24. [Google Scholar] [CrossRef] [PubMed]
  41. Mekheimer, R.; Hilmy, N.M.; Abdel Hameed, A.; Dacrory, S.; Sadek, K.U. Simple, three component, highly efficient green synthesis of thiazolo[3,2-a]pyridine derivatives under neat conditions. Synth. Commun. 2011, 41, 2511–2516. [Google Scholar] [CrossRef]
Sample Availability: Samples of the compounds 4a–k are available from the authors.
Molecules 17 06011 sch001 550
Scheme 1. One-pot synthesis of 2-arylbenzothiazoles 4a–k.
Scheme 1. One-pot synthesis of 2-arylbenzothiazoles 4a–k.
Molecules 17 06011 sch001
Molecules 17 06011 sch002 550
Scheme 2. A proposed mechanism for the formation of 2-arylbenzothiazoles 4a–k.
Scheme 2. A proposed mechanism for the formation of 2-arylbenzothiazoles 4a–k.
Molecules 17 06011 sch002

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MDPI and ACS Style

Sadek, K.U.; Mekheimer, R.A.; Hameed, A.M.A.; Elnahas, F.; Elnagdi, M.H. Green and Highly Efficient Synthesis of 2-Arylbenzothiazoles Using Glycerol without Catalyst at Ambient Temperature. Molecules 2012, 17, 6011-6019. https://doi.org/10.3390/molecules17056011

AMA Style

Sadek KU, Mekheimer RA, Hameed AMA, Elnahas F, Elnagdi MH. Green and Highly Efficient Synthesis of 2-Arylbenzothiazoles Using Glycerol without Catalyst at Ambient Temperature. Molecules. 2012; 17(5):6011-6019. https://doi.org/10.3390/molecules17056011

Chicago/Turabian Style

Sadek, Kamal Usef, Ramadan Ahmed Mekheimer, Afaf Mohamed Abdel Hameed, Fatma Elnahas, and Mohamed Hilmy Elnagdi. 2012. "Green and Highly Efficient Synthesis of 2-Arylbenzothiazoles Using Glycerol without Catalyst at Ambient Temperature" Molecules 17, no. 5: 6011-6019. https://doi.org/10.3390/molecules17056011

APA Style

Sadek, K. U., Mekheimer, R. A., Hameed, A. M. A., Elnahas, F., & Elnagdi, M. H. (2012). Green and Highly Efficient Synthesis of 2-Arylbenzothiazoles Using Glycerol without Catalyst at Ambient Temperature. Molecules, 17(5), 6011-6019. https://doi.org/10.3390/molecules17056011

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