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Synlett 2008(19): 2941-2944  
DOI: 10.1055/s-0028-1083623
LETTER
© Georg Thieme Verlag Stuttgart ˙ New York

Efficient Synthesis of Imidazo[2,1-b][1,3]benzothiazoles and 9H-Imidazo-[1,2-a][1,3]benzimidazoles under Solvent-Free Conditions

Mehdi Adib*a, Esmail Sheibania, Long-Guan Zhub, Hamid Reza Bijanzadehc
a School of Chemistry, University College of Science, University of Tehran, 14155-6455 Tehran, Iran
Fax: +98(21)66495291; e-Mail: madib@khayam.ut.ac.ir;
b Chemistry Department, Zhejiang University, Hangzhou 310027, P. R. of China
c Department of Chemistry, Tarbiat Modarres University, 14115-175 Tehran, Iran
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Publication History

Received 1 August 2008
Publication Date:
12 November 2008 (online)

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Abstract

An efficient synthesis of imidazo[2,1-b][1,3]benzothiazoles and 9H-imidazo[1,2-a][1,3]benzimidazoles is described from a novel multicomponent reaction between 2-aminobenzothiazoles or 2-aminobenzimidazole, benzaldehydes, and imidazoline-2,4,5-trione under solvent-free conditions.

Key words

imidazo[2,1-b][1,3]benzothiazoles - 9H-imidazo[1,2-a][1,3]benzimidazoles - imidazoline-2,4,5-trione - multicomponent reactions - solvent-free synthesis - heterocycles

    References and Notes

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18

Procedure for the Preparation of 2-(4-Methylphenyl)- N ³ -[( E )-1-(4-methylphenyl)methylidene]imidazo[2,1- b ]-[1,3]benzothiazol-3-amine (6a)
A mixture of 2-aminobenzothiazole (0.30 g, 2 mmol),
4-methylbenzaldehyde (0.60 g, 5 mmol), and imidazoline-2,4,5-trione (0.34 g, 3 mmol) was stirred at 200 ˚C for 5 min. Then, the reaction mixture was cooled to r.t. and the residue was purified by column chromatography using n-hexane-EtOAc (1:3) as eluent. The solvent was removed and the product was recrystallized from n-hexane-EtOAc (1:1). The product 6a was obtained as yellow crystals; yield 0.70 g (92%, relative to 2-aminobenzothiazole). IR (KBr): 1603, 1495, 1479, 1379, 1352, 1315, 1175, 1146, 1109, 820, 748 cm-¹. ¹H NMR (500.1 MHz, CDCl3): δ = 2.37, 2.45 (2 × s, 6 H, 2 × CH3), 7.19 (d, J = 7.4 Hz, 2 H, 2 × CH), 7.29-7.32 (m, 3 H, 3 × CH), 7.42 (dd, J = 7.9, 7.4 Hz, 1 H, CH), 7.64-7.68 (m, 3 H, 3 × CH), 7.76 (d, J = 7.4 Hz, 2 H, 2 × CH), 8.27 (d, J = 8.0 Hz, 1 H, CH), 8.74 (s, 1 H, CH). ¹³C NMR (125.8 MHz, CDCl3): δ = 21.30, 21.70 (2 × CH3), 115.03, 123.79, 124.45, 126.18, 127.32, 128.60, 129.52, 129.70 (8 × CH), 130.27, 131.88, 133.25, 133.36, 133.61, 135.18, 137.10, 142.32, 144.98 (9 × C), 159.89 (CH). MS: m/z (%) = 381 (100) [M+], 366 (10), 289 (4), 251 (85), 134 (16), 103 (7), 91 (14), 77 (7), 65 (5). Anal. Calcd (%) for C24H19N3S (381.50): C, 75.56; H, 5.02; N, 11.01. Found: C, 75.5; H, 5.2; N, 10.9.
Compound 6d: yellow crystals; yield 0.75 g (97%). IR (KBr): 1603, 1589, 1528, 1500, 1491, 1454, 1379, 1290, 1225, 1192, 1148, 1092, 845, 752 cm-¹. ¹H NMR (500.1 MHz, CDCl3): δ = 7.09 (dd, ³ J FH = 8.6 Hz, ³ J HH = 8.7 Hz, 2 H, 2 × CH), 7.20 (dd, ³ J FH = 8.6 Hz, ³ J HH = 8.7 Hz, 2 H,
2 × CH), 7.35 (dd, J = 8.1, 7.2 Hz, 1 H, CH), 7.45 (dd, J = 8.1, 7.2 Hz, 1 H, CH), 7.69 (d, J = 7.2 Hz, 1 H, CH), 7.72 (dd, 4 J FH = 5.4 Hz, ³ J HH = 8.7 Hz, 2 H, 2 × CH), 7.86 (dd, 4 J FH = 5.5 Hz, ³ J HH = 8.7 Hz, 2 H, 2 × CH), 8.24 (d, J = 8.1 Hz, 1 H, CH), 8.67 (s, 1 H, CH). ¹³C NMR (125.8 MHz, CDCl3): δ = 114.94 (CH), 115.87 (d, ² J FC = 21.5 Hz, CH), 116.27 (d, ² J FC = 22.1 Hz, CH), 123.93, 124.71, 126.29 (3 × CH), 129.34 (d, ³ J FC = 7.9 Hz, CH), 130.30 (C), 130.56 (d, ³ J FC = 8.8 Hz, CH), 130.82 (d, 4 J FC = 3.3 Hz, C), 132.30 (d, 4 J FC = 3.2 Hz, C), 132.56, 133.21, 134.89, 145.43 (4 × C), 158.47 (CH), 162.20 (d, ¹ J FC = 247.3 Hz, CF), 165.05 (d, ¹ J FC = 253.7 Hz, CF). MS: m/z (%) = 389 (98) [M+], 350 (32), 326 (8), 255 (100), 229 (27), 201 (13), 134 (37), 107 (15), 90 (9). Anal. Calcd (%) for C22H13F2N3S (389.43): C, 67.85; H, 3.36; N, 10.79. Found: C, 67.8; H, 3.4; N, 10.7.
Compound 6g: yellow crystals; yield: 0.68 g (92%). IR (KBr): 3290 (NH), 1601, 1585, 1528, 1510, 1493, 1450, 1339, 1232, 1225, 1196, 1150, 1094, 839, 768 cm-¹. ¹H NMR (500.1 MHz, DMSO-d 6): δ = 7.19 (dd, J = 7.8, 7.6 Hz, 1 H, CH), 7.25 (dd, ³ J FH = 8.6 Hz, ³ J HH = 8.7 Hz, 2 H,
2 × CH), 7.31 (dd, J = 7.8, 7.6 Hz, 1 H, CH), 7.37 (dd, ³ J FH = 8.6 Hz, ³ J HH = 8.7 Hz, 2 H, 2 × CH), 7.43 (d, J = 7.8 Hz, 1 H, CH), 7.71 (d, J = 8.0 Hz, 1 H, CH), 8.04 (dd, 4 J FH = 5.3 Hz, ³ J HH = 8.7 Hz, 2 H, 2 × CH), 8.19 (dd, 4 J FH = 5.4 Hz, ³ J HH = 8.7 Hz, 2 H, 2 × CH), 8.86 (s, 1 H, CH), 12.00 (br, 1 H, NH). ¹³C NMR (125.8 MHz, DMSO-d 6): δ = 112.04, 112.36 (2 × CH), 115.04 (d, ² J FC = 21.4 Hz, CH), 116.00 (d, ² J FC = 22.0 Hz, CH), 119.84, 123.61 (2 × CH), 124.98, 127.37 (2 × C), 129.18 (d, ³ J FC = 7.9 Hz, CH), 130.03 (d, ³ J FC = 8.7 Hz, CH), 131.22 (d, 4 J FC = 3.3 Hz, C), 133.29 (d, 4 J FC = 3.2 Hz, C), 136.45, 138.98, 148.09 (3 × C), 150.49 (CH), 162.41 (d, ¹ J FC = 247.9 Hz, CF), 164.95 (d, ¹ J FC = 252.5 Hz, CF). MS: m/z (%) = 372 (19) [M+], 360 (15), 326 (97), 238 (91), 229 (23), 196 (100), 133 (33), 118 (43), 107 (19), 95 (35), 79 (44), 69 (16). Anal. Calcd (%) for C22H14F2N4 (372.38): C, 70.96; H, 3.79; N, 15.05. Found: C, 71.0; H, 3.8; N, 14.9.

19

Selected X-ray Crystallographic Data for Compound 6a
C24H19N3S, monoclinic, space group = P21/n, a = 12.7579 (12) Å, b = 7.5112 (7) Å, c = 21.2243 (20) Å, β = 91.626 (2)˚, V = 2033.03 (3) ų, T = 295 (2) K, Z = 4, D calcd = 1.25 g cm-³, µ = 0.173 mm-¹, 2245 observed reflections, final R 1 = 0.079, wR 2 = 0.149 and for all data R 1 = 0.137, wR 2 = 0.172. CCDC 671151 contains the supplementary crystallographic data for the structure reported in this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data_request/cif.