2002The Journal of Organic ChemistryRequires access

An Effective Procedure for the Acylation of Azaindoles at C-3

Zhongxing Zhang, Zhong Yang, Henry Ν. C. Wong, Juliang Zhu, Nicholas A. Meanwell, John F. Kadow, Tao Wang

Open publisher page 54 citations

Abstract

Conditions for attachment of acetyl chloride, benzoyl chloride, and chloromethyl oxalate to the 3-position of 4-, 5-, 6-, or 7-azaindoles were explored. Best results were achieved with an excess of AlCl(3) in CH(2)Cl(2) followed by the addition of an acyl chloride at room temperature.

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What this paper is about

Conditions for attachment of acetyl chloride, benzoyl chloride, and chloromethyl oxalate to the 3-position of 4-, 5-, 6-, or 7-azaindoles were explored. Best results were achieved with an excess of AlCl(3) in CH(2)Cl(2) followed by the addition of an acyl chloride at room temperature.

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Available abstract

Conditions for attachment of acetyl chloride, benzoyl chloride, and chloromethyl oxalate to the 3-position of 4-, 5-, 6-, or 7-azaindoles were explored. Best results were achieved with an excess of AlCl(3) in CH(2)Cl(2) followed by the addition of an acyl chloride at room temperature.

Key concepts: Chemistry, Acylation, Combinatorial chemistry, Organic chemistry, Catalysis

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