5-ethyl-1-(3-phenyl-2,1-benzisoxazol-5-yl)-1H-1,2,3-triazole-4-carboxylic acid

Base Information

Chemical Name:5-ethyl-1-(3-phenyl-2,1-benzisoxazol-5-yl)-1H-1,2,3-triazole-4-carboxylic acid
CAS No.:1017426-83-3
Molecular Formula:C₁₈H₁₄N₄O₃
Molecular Weight:334.334
Hs Code.:

Synonyms:5-ethyl-1-(3-phenyl-2,1-benzisoxazol-5-yl)-1H-1,2,3-triazole-4-carboxylic acid

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 5-ethyl-1-(3-phenyl-2,1-benzisoxazol-5-yl)-1H-1,2,3-triazole-4-carboxylic acid

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Technology Process of 5-ethyl-1-(3-phenyl-2,1-benzisoxazol-5-yl)-1H-1,2,3-triazole-4-carboxylic acid

There total 1 articles about 5-ethyl-1-(3-phenyl-2,1-benzisoxazol-5-yl)-1H-1,2,3-triazole-4-carboxylic acid which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 88.0%

: 1097045-91-4
5-ethyl-1-(4-nitrophenyl)-1H-1,2,3-triazole-4-carboxylic acid

: 140-29-4
phenylacetonitrile

: 1017426-83-3
5-ethyl-1-(3-phenyl-2,1-benzisoxazol-5-yl)-1H-1,2,3-triazole-4-carboxylic acid

Guidance literature:: With sodium hydroxide; In ethanol; at 20 - 60 ℃; for 28h;
DOI:10.1055/s-0029-1216875

Reference yield:

: 1017426-83-3
5-ethyl-1-(3-phenyl-2,1-benzisoxazol-5-yl)-1H-1,2,3-triazole-4-carboxylic acid

: C₁₈H₁₃ClN₄O₂

Guidance literature:: With oxalyl dichloride; In dichloromethane; N,N-dimethyl-formamide; at 0 - 20 ℃; for 3.25h;
DOI:10.1007/s00044-013-0841-8

Reference yield:

: 1017426-83-3
5-ethyl-1-(3-phenyl-2,1-benzisoxazol-5-yl)-1H-1,2,3-triazole-4-carboxylic acid

: 1147207-92-8
N-(2-chlorophenyl)-5-ethyl-1-(3-phenyl-2,1-benzoxazol-5-yl)-1H-1,2,3-triazole-4-carboxamide

Guidance literature:: Multi-step reaction with 2 steps

1: oxalyl dichloride / dichloromethane; N,N-dimethyl-formamide / 3.25 h / 0 - 20 °C

2: triethylamine / dichloromethane / 0 - 20 °C

With oxalyl dichloride; triethylamine; In dichloromethane; N,N-dimethyl-formamide;
DOI:10.1007/s00044-013-0841-8