Issue 8, 1977

Reaction of 5-chloropyridin-2-yl-thioureas with phenacyl bromides: a new thiazole synthesis. X-Ray crystal structure of 5-(5-chloropyridin-2-yl)-2-diethylamino-4-phenylthiazole

Abstract

The reaction of N-(5-chloropyridin-2-yl)-NN′-dialkylthioureas with phenacyl bromides yields trisubstituted thiazoles via a 1,3-pyridyl shift; the X-ray crystal structure of one of these, 5-(5-chloropyridin-2-yl)-2-diethylamino-4-phenylthiazole, has been determined.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1977, 282-283

Reaction of 5-chloropyridin-2-yl-thioureas with phenacyl bromides: a new thiazole synthesis. X-Ray crystal structure of 5-(5-chloropyridin-2-yl)-2-diethylamino-4-phenylthiazole

D. J. Le Count and J. A. J. Jarvis, J. Chem. Soc., Chem. Commun., 1977, 282 DOI: 10.1039/C39770000282

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