Conversion of 2-Amino-4-chloro-3-methylbenzenethiol into Bioactive Heterocycles Containing 1,4-Thiazine Nucleus: Phenothiazine Tranquillizers
Corresponding Author(s) : R.K. Rathore
Asian Journal of Chemistry,
Vol. 9 No. 4 (1997): Vol 9 Issue 4
Abstract
A convenient synthesis of some heterocycles containing 1,4-thiazine nucleus is reported. It involves the condensation and oxidative cyclization of 2-amino-4-chloro-3-methylbenzenethiol with 2-mino/2, 6-dihalonitrobenzenes. The structures of the synthesized compounds have been characterized by the analytical and structural studied.
Keywords
2-Amino-4-chloro-3-methylbenzenethiol
Bioactive Heterocycles
1,4-Thiazine Nucleus
Phenothiazine Tranquillizers
Rathore, R., & Gupta, R. (2012). Conversion of 2-Amino-4-chloro-3-methylbenzenethiol into Bioactive Heterocycles Containing 1,4-Thiazine Nucleus: Phenothiazine Tranquillizers. Asian Journal of Chemistry, 9(4), 672–676. Retrieved from https://asianpubs.org/index.php/ajchem/article/view/23945
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