“…These reactions can be carried out for some hours at room temperature or by heating at steam bath (Scheme 9). [24][25][26][27][28] Treatment of 2-chlorobenzothiazole 28 with thiourea 27 gave benzo[d]thiazol-2-yl carbamimidothioate 29 (Scheme 10). [29] 5-Methyl-N-phenylthiazol-2-amine 46 can be organized by intramolecular nucleophilic substitutionreaction of 1-(2-bromoallyl)-3-phenylthiourea 45 (Scheme 16).…”
“…These reactions can be carried out for some hours at room temperature or by heating at steam bath (Scheme 9). [24][25][26][27][28] Treatment of 2-chlorobenzothiazole 28 with thiourea 27 gave benzo[d]thiazol-2-yl carbamimidothioate 29 (Scheme 10). [29] 5-Methyl-N-phenylthiazol-2-amine 46 can be organized by intramolecular nucleophilic substitutionreaction of 1-(2-bromoallyl)-3-phenylthiourea 45 (Scheme 16).…”
“…Tcherniac [20] reported the synthesis of 4-methyl-2-thiazolinone (4) and Ganapathi and Venkataraman [21] reported the preparation of ethyl 4-methyl-2-thiazolinone-5-carboxylate (5) and 4-methyl-5-acetyl-2-thiazolinone (6) by the following reactions: If 2 is allowed to dry longer than two hours or comes in contact with metals it decomposes.…”
Section: Ch3cnmentioning
confidence: 99%
“…Venkataraman [21] were employed for the synthesis of 4-6. To a stirrcvi solution at "-10' rontaining 84.6 g (0.9 mole) of 2 in water or acetonv water (Table I), 0.8 mole of chloroacetone, ethyl ol-rhloroacetoacrtatl, or 3-chloro-2,4-pentanedione was added in one portion.…”
Section: Modified Procedures Described By Tcherniac [20] and Ganapathmentioning
“…Reaction of ethyl 2-phenyl-4-methylthiazole-5carboxylate (111) (10) with N-bromosuccinimide gave ethyl 2-phenyl-4-bromomethylthiazole-5-carboxylate (IV). Reaction of the latter with phenol according to the procedure reported previously (1 1) afforded ethyl 2-phenyl-4phenoxymethylthiazole-5-carboxylate (Va).…”
Aus den 4‐Methyl‐thiazolen (Ia) entstehen die funktionellen Derivate (Ic) und (Id), die über die freien Säuren (II) und die Säurechloride (III) zu den Cyclisierungsprodukten (IV) führen.
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