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Reaction products of 2‐aminobenzenethiol with some β‐diketones
Author(s) -
Alyea Elmer C.,
Malek Abdul
Publication year - 1985
Publication title -
journal of heterocyclic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.321
H-Index - 59
eISSN - 1943-5193
pISSN - 0022-152X
DOI - 10.1002/jhet.5570220536
Subject(s) - chemistry , condensation , condensation reaction , organic chemistry , bicyclic molecule , isolation (microbiology) , combinatorial chemistry , medicinal chemistry , catalysis , physics , thermodynamics , biology , microbiology and biotechnology
2‐Aminobenzenethiol undergoes condensation reactions with several β‐diketones (CH 3 , CF 3 and C 6 H 5 substituents) to form benzothiazolines. Conversion to benzothiazines and benzothiazoles occurs in some instances, as documented by the isolation and spectroscopic characterization of the products.