Iodo derivatives of 5-methyl-1-phenyl-1,2,3-triazolecarboxylic acid
✍ Scribed by H. N. Bojarska-Dahlig
- Book ID
- 104586413
- Publisher
- Elsevier Science
- Year
- 2010
- Tongue
- English
- Weight
- 374 KB
- Volume
- 80
- Category
- Article
- ISSN
- 0165-0513
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✦ Synopsis
Abstract
1‐(3′‐Iodophenyl)‐5‐methyl‐1,2,3‐triazolecarboxylic acid, 1‐(4′‐iodophenyl)‐5‐methyl‐1,2,3‐triazolecarboxylic acid and 1‐(3′‐4′‐di‐iodophenyl)‐5‐methyl‐1,2,3‐triazolecarboxylic acid were prepared by reacting ethyl acetylacetate with the corresponding 1‐azido‐di‐iodobenzene.
5‐Methyl‐1‐phenyl‐1,2,3‐triazolecarbonyl chloride and 1‐(4′‐iodophenyl)‐5‐methyl‐1,2,3‐triazolecarbonyl chloride were condensed with 3‐amino‐2,4,6‐tri‐iodobenzoic acid, α‐ethyl‐3‐amino‐2,4,6‐tri‐iodohydrocinnamic (iopanoic) acid and α‐ethyl‐3‐amino‐2,4,6‐tri‐iodocinnamic (dehydroiopanoic) acid.
📜 SIMILAR VOLUMES
In the crystal structure of the title compound, C 16 H 14 I 2 N 2 , the molecule lies on a crystallographic inversion center and hence the two imine groups are mutually trans.
## Abstract The triazaphosphole __1__ adds sulfur along with HCl or H~2~S to yield, respectively, the dihydrotriazaphosphole thiochloride __4__ and sesquisulfide __5__ (two diastereomers). In pyridine solution, __1__ adds sulfur alone to yield the trimer of a triazaphosphole monosulfide __7__. Its