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Synthesis of [1,2,5]selena(or thia)diazolo[3,4-e][1,4]diazepines, [1,2,5]selena(or thia)diazolo[3,4-e][1,4]oxazepines and [1,2,5]selena(or thia)diazolo[3,4-c] [1,2,6]thiadiazines

✍ Scribed by Taisei Ueda; Wataru Doi; Shin-Ichi Nagai; Jinsaku Sakakibara


Publisher
Journal of Heterocyclic Chemistry
Year
2000
Tongue
English
Weight
270 KB
Volume
37
Category
Article
ISSN
0022-152X

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✦ Synopsis


Abstract

Novel heterocycles [1,2,5]selenadiazolo[3,4‐e][1,4]diazepines 3a‐c, [1,2,5]thiadiazolo[3,4‐e]‐[1,4]diazepines 7a‐c, [1,2,5]selenadiazolo[3,4‐e][1,4]oxaepines 4a,b, [1,2,5]thiadiazolo[3,4‐e]‐[1,4]oxazepines 9a‐c and [1,2,5]selena(or thia)diazolo[3,4‐c][1,2,6]thiadiazines 10a,b were synthesized starting form 4,6‐dimethyl[1,2,5]se]enadiazolo[3,4‐d]pyrimidine‐5,7(4__H__,6__H__)‐dione 1 or 4,6‐dimethyl‐[1,2,5]thiadiazolo[3,4‐d]pyrimidine‐5,7(4__H__,6__H__)‐dione 5.


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Syntheses of [1,2,3]selenadiazolo[4,5-e]
✍ M. Shekarchi; F. Ellahiyan; T. Akbarzadeh; A. Shafiee 📂 Article 📅 2003 🏛 Journal of Heterocyclic Chemistry 🌐 English ⚖ 85 KB 👁 1 views

## Abstract Dehydrogenation of ethyl 3‐methyl‐4‐oxo‐4,5,6,7‐tetrahydrobenzofuran‐2‐carboxylate 1 with 2,2′‐azobi‐sisobutyronitrile and __N__‐bromosuccinimide gave ethyl 4‐hydroxy‐3‐methylbenzofuran‐2‐carboxylate **3**. Reaction of compounds **3–4** with hydrazine hydrate afforded the corresponding