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
Generation of 6,7-Dihydro-5H-1,3,4-thiadiazolo[3,2-a]pyridines — Unexpected Products in the Reaction of 5-Ethylthio-1,3,4-thiadiazole-2-amine and 3-(Dimethylamino)propiophenones
✍ Scribed by Jairo Quiroga; Braulio Insuasty; Pedro Hernandez; Rodolfo Moreno; Regina H. de Almeida; Herbert Meier
- Publisher
- John Wiley and Sons
- Year
- 1998
- Tongue
- English
- Weight
- 447 KB
- Volume
- 1998
- Category
- Article
- ISSN
- 1434-193X
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✦ Synopsis
pyridines 4a-e was prepared by the reaction of 5-ethylthio-1,3,4-thiadiazole-2-amine (1) and p-substituted 3-(dimeth-1,3,4-Thiadiazoles find a variety of applications as antibiotic, antiinflammatory or bacteriostatic agents and as pesticides [1] [2] . These biological activities have stimulated us to synthesize and investigate a new class of fused 1,3,4-thiadiazoles. Based on our experience [3] [4] [5] [6] with the reaction Scheme 1
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