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Syntheses of some new 4-amino-5-(N-methyl-arylsulfonamido)methyl-1,2,4-triazole-3-thiones and their derivatives

✍ Scribed by Guofeng Jia; Zhengming Li


Publisher
John Wiley and Sons
Year
1996
Tongue
English
Weight
281 KB
Volume
7
Category
Article
ISSN
1042-7163

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✦ Synopsis


The cyclization of 4-arnino-5-(N-methyl-arylsulfonarnido) methyl-1,2,4-triazole-3-thiones 11, synthesized by the Reid and Heindel approach, with a-chloroacetophenone yields 7H-6-aryl-3-(N-rnethyl-arylsulfonarnido) methyl-s-triazob[3,4-b][l, 3,4]-thiazines 111.

Novel compounds I1 also react with benzyl chloride to afford 4-amino-3-benzyIthio-5-(N-rnethyl-arylsulfon- arnido)methyl-1,2,$-triazole IV.0 I996 John Wiley & Sons, Inc.


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A series of 4-(alkylidene/arylidene)amino-5-(2-furanyl)-2.4-dihydro-3H-I .2.4-triazolc-3-1hiones (2) and 6-aryl-3-(2-furanyl)-7H-12.4-triazolo[3,4-b]( 1.3.41 thiadiazines (3) werc synthesized. The configuration of 2g was assigned on che basis of 'H-NMR data. Of the new derivatives tesced. only 2b. 2