A VERSATILE SYNTHESIS OF FUNCTIONALIZED 2-AMINOQUINOLINES BY MERCURY CONTROLLED CYCLIZATION OF 2-VINYLPHENYLTHIOUREAS

Authors
WIGGALL KJ RICHARDSON SK
Citation
Kj. Wiggall et Sk. Richardson, A VERSATILE SYNTHESIS OF FUNCTIONALIZED 2-AMINOQUINOLINES BY MERCURY CONTROLLED CYCLIZATION OF 2-VINYLPHENYLTHIOUREAS, Journal of heterocyclic chemistry, 32(3), 1995, pp. 867-870
Citations number
10
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Journal of heterocyclic chemistry → ACNP
ISSN journal
0022152X
Volume
32
Issue
3
Year of publication
1995
Pages
867 - 870
Database
ISI
SICI code
0022-152X(1995)32:3<867:AVSOF2>2.0.ZU;2-K
Abstract
-(4-Hydroxyphenyl)-2-phenylamino-1,8-naphthyridine was prepared via cy clisation of N'-3-(4-hydroxyphenethen-1-yl)pyridin-2-ylthiourea in the presence of mercuric oxide. Derivatives of 4-methyl-2-aminoquinolines were prepared in a similar manner from 2-vinylphenylthioureas.