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Synthesis of Tofisopam by Way of Photoinduced CO 2 Fixation
Author(s) -
Masuda Yusuke,
Makita Katsuhiko,
Ishida Naoki,
Murakami Masahiro
Publication year - 2019
Publication title -
chemistry – an asian journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.18
H-Index - 106
eISSN - 1861-471X
pISSN - 1861-4728
DOI - 10.1002/asia.201901431
Subject(s) - chemistry , carboxylation , carbon fixation , triple bond , acylation , combinatorial chemistry , medicinal chemistry , stereochemistry , organic chemistry , double bond , catalysis , carbon dioxide
Herein reported is a unique synthetic route of Tofisopam, an anxiolytic drug containing a 2,3‐benzodiazepine core structure. 3,4‐Dimethoxypropylbenzene and 3,4‐dimethoxybenzoic acid, which are both of plant origin, and CO 2 constitute its carbon skeleton. These three renewable substances are united by two C−C bond forming reactions, i.e., a Friedel–Crafts acylation reaction and a photoinduced carboxylation reaction to construct the major carbon framework. Finally, a methyl group is introduced by a Kumada‐type cross‐coupling reaction to furnish Tofisopam. Various analogs of Tofisopam are readily synthesized by introducing other substituents than a methyl group at the last C−C bond forming step.