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Synthesis of Ethyl 2‐Arylaminoimidazo[2,1‐b]benzothiazole‐3‐carboxylates
Author(s) -
Khalafy Jabbar,
Ebrahimlo Ali Reza Molla,
Dilmaghani Karim Akbari
Publication year - 2004
Publication title -
journal of the chinese chemical society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.329
H-Index - 45
eISSN - 2192-6549
pISSN - 0009-4536
DOI - 10.1002/jccs.200400196
Subject(s) - benzothiazole , chemistry , triethylamine , aryl , medicinal chemistry , ethanol , nitrogen , organic chemistry , alkyl
3‐Arylamino‐4‐ethoxycarbonylisoxazol‐5(2H)‐ones, substituted on nitrogen with a benzothiazole group, reacts with triethylamine in ethanol under reflux conditions to provide a convenient synthesis of ethyl 2‐aryl‐aminoimidazo[2,1‐b]benzothiazole‐3‐carboxylates.
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