1,2,4-Triazolo[1,2-a]benzotriazoles: first examples of a novel ring system
✍ Scribed by Alan R Katritzky; Tian-Bao Huang; Peter J Steel
- Publisher
- Elsevier Science
- Year
- 2001
- Tongue
- French
- Weight
- 80 KB
- Volume
- 42
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
a-Benzotriazolylamides 6a-d afforded N-(benzotriazol-1-ylmethyl)arylimidoyl chlorides (4a-d), which reacted in situ with potassium tert-butoxide to form 3-aryl-1,2,4-triazolo[1,2-a]benzotriazoles (7a-d) (44-68%), representatives of a novel heterocyclic system. The structure of 7a was confirmed by single crystal X-ray analysis.
📜 SIMILAR VOLUMES
## Abstract Reaction of 1‐amino‐3‐arylpyrido[1,2‐__a__]benzimidazole‐2,4‐dicarbonitrile **(1)** with dimethylformamide‐dimethylacetal (DMF‐DMA) gave **1**‐[__N,N__‐(dimethylaminomethylene)amino]‐3‐arylpyrido[1,2‐__a__]benzimidazole‐2,4‐dicarbonitrile **(2).** Compounds **(1)** reacted with triethyl
1-Amino-1H-benzimidazol-2-yl)methanol 1 with thionyl chloride at reflux afforded 3-chlorobenzimidazo [1,2c][1,2,3]thiadiazole 4, which reacted with various nucleophiles to give different products depending on the nature of the solvent. The structures of 4 and di(benzimidazo[1,2-c][1,2,3]thiadiazol-3
Dianion 2 derived from N-Boc-aminobenzotriazole 1 condenses in a [1.2]fashion with ct, fl-unsaturated aldehydes; subsequent oxidation of the resulting allylic alcohols 7 using manganese(IV) oxide or, less effectively, treatment of the derived acetates 10 with Pd(O), results in direct formation of th