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IJC-B Vol.48B [2009] >
IJC-B Vol.48B(06) [June 2009] >


Title: 2-(2-Alkylamino-4-aminothiazol-5-oyl)-N-methylbenzimidazoles: Synthesis and the effect of intra molecular H-bonding in 1H NMR
Authors: Reji, T F Abbs Fen
Rajasekharan, K N
Keywords: Analogs
dendrodoine
cytotoxic
thiazole
N-methylbenzimidazoles
Issue Date: Jun-2009
Publisher: CSIR
Abstract: 2-(2-Alkylamino-4-aminothiazol-5-oyl)-N-methylbenzimi¬≠da¬≠zoles, as the analogs of the cytotoxic marine alkaloid dendrodoine, is synthesized and characterized by elemental analysis, IR, NMR and mass spectral data. The thiourea derivatives provide four ring atoms for the thiazole ring construction and thus act as [C-N-C-S] synthons. The remaining carbon of the thiazole is sourced from 2-(2-bromoacetyl)-N-methylbenzimidazole. This [4+1] heterocyclization reaction is adopted for the synthesis of novel benzimidazole derivatives. The presence of two signals in the 1H NMR spectrum arising from the NH2 hydrogens shows that the two hydrogens are not exchanging rapidly on the chemical shift time scale and they are in two different chemical environments due to H-bonding.
Page(s): 877-881
ISSN: 0376-4699
Source:IJC-B Vol.48B(06) [June 2009]

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