Stereospecific synthesis of 6,7-dihydro-5H-1,2,4-triazolo[3,4-b][1,3,4]thiadiazines
β Scribed by Yehia A. Ibrahim; Ahmed H. M. Elwahy; Ayman E. M. El-Fiky
- Publisher
- John Wiley and Sons
- Year
- 1994
- Tongue
- English
- Weight
- 319 KB
- Volume
- 5
- Category
- Article
- ISSN
- 1042-7163
No coin nor oath required. For personal study only.
β¦ Synopsis
The reaction of 3-mercapto-4-aryIideneamino-l,2,4triazoles 2b-d, 3a-d with ethyl bromoacetate and/or phenacyl bromide in hot DMF and triethylamine affords the stereochemically pure 7-acyl-6-aryl-6,7dihydro-5H-lt2, 4-triazolo[3,4-b][l, 3,4]thiadiazines
π SIMILAR VOLUMES
## Abstract [1,2,4]Triazolo[3,4βb][1,3,4]thiadiazines **2a**, **2b**, **2c**, **2d**, **2e**, **2f** and 3,7βdimethylβ4__H__β[1,2,4]triazino[3,4βb][1,3,4]thiadiazinβ6βone **4** were synthesized by oneβpot cyclocondensation reaction with Ξ±βchloroacetonitrile and Ξ±βhaloketones in the presence of cata
## Abstract For Abstract see ChemInform Abstract in Full Text.