Chemical and Pharmaceutical Bulletin
Online ISSN : 1347-5223
Print ISSN : 0009-2363
ISSN-L : 0009-2363
Synthetic Studies on Indoles and Related Compounds. XII. A Simple General Method for the C-3 Acylation of Ethyl Indole-2-carboxylates
YASUOKI MURAKAMIMASANOBU TANIMICHIO SUZUKIKEIZO SUDOHMIDORI UESATOKENJIRO TANAKAYUUSAKU YOKOYAMA
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1985 Volume 33 Issue 11 Pages 4707-4716

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Abstract
Ethyl indole-2-carboxylate (1a) and its derivatives were reacted with various carboxylic acids by using trifluoroacetic anhydride and phosphoric acid (or polyphosphoric acid) to yield effectively the corresponding ethyl 3-acylindole-2-carboxylates (3). However, strongly acidic carboxylic acids and nitrogen-containing carboxylic acids were poor acylating agents. Ethyl 3-acylindole-2-carboxylate (3) could easily be converted to 3-acylindole (5)
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© The Pharmaceutical Society of Japan
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