Volume 31, Issue 23
Heterocyclic Compounds
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ChemInform Abstract: A Facile Access to 2-Methylthio/Alkoxy/Amino-3-acylimidazo[1,2-a]pyridines Based on Cupric Chloride Promoted Oxidative Ring Closure of α-Oxoketene N,S-, N,O-, and N,N-Acetals.

Okram Barun

Okram Barun

Dep. Chem., Indian Inst. Technol., Kanpur 208 016, India

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H. Ila

H. Ila

Dep. Chem., Indian Inst. Technol., Kanpur 208 016, India

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H. Junjappa

H. Junjappa

Dep. Chem., Indian Inst. Technol., Kanpur 208 016, India

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Okram Mukherjee Singh

Okram Mukherjee Singh

Dep. Chem., Indian Inst. Technol., Kanpur 208 016, India

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First published: 08 June 2010

Abstract

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ChemInform Abstract

α-Oxoketene N,S- N,O-, and N,N acetals, easily accessible from aminoheterocycles, undergo under mild conditions in the presence of CuCl2 an unprecedented cyclization to give 2-methylthio-, 2-methoxy-, and 2-aminoimidazopyridines in good yields. A few of these compounds are further subjected to reductive dethiomethylation or cyclodehydration to give products (III) and (VI) respectively.

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