N-(4-chlorophenyl)-5-methyl-1-phenyl-1H-1,2,3-triazole-4-carboxamide

Base Information

Chemical Name:N-(4-chlorophenyl)-5-methyl-1-phenyl-1H-1,2,3-triazole-4-carboxamide
CAS No.:866845-57-0
Molecular Formula:C₁₆H₁₃ClN₄O
Molecular Weight:312.758
Hs Code.:
Mol file:866845-57-0.mol

Synonyms:N-(4-chlorophenyl)-5-methyl-1-phenyl-1H-1,2,3-triazole-4-carboxamide

Suppliers and Price of N-(4-chlorophenyl)-5-methyl-1-phenyl-1H-1,2,3-triazole-4-carboxamide

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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 N-(4-chlorophenyl)-5-methyl-1-phenyl-1H-1,2,3-triazole-4-carboxamide

Chemical Property:

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Technology Process of N-(4-chlorophenyl)-5-methyl-1-phenyl-1H-1,2,3-triazole-4-carboxamide

There total 3 articles about N-(4-chlorophenyl)-5-methyl-1-phenyl-1H-1,2,3-triazole-4-carboxamide 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: 87.0%

: 101-92-8
4'-Chloroacetoacetanilide

: 622-37-7
Phenyl azide

N-(4-chlorophenyl)-5-methyl-1-phenyl-1H-1,2,3-triazole-4-carboxamide: 866845-57-0
N-(4-chlorophenyl)-5-methyl-1-phenyl-1H-1,2,3-triazole-4-carboxamide

Guidance literature:: With 1,8-diazabicyclo[5.4.0]undec-7-ene; In chloroform; at 20 ℃; for 24h; regioselective reaction;
DOI:10.1002/ejoc.201600157

Reference yield: 79.0%

: 62-53-3
aniline

: 170944-20-4
2-diazo-3-oxo-N-(4-chlorophenyl)-butanamide

N-(4-chlorophenyl)-5-methyl-1-phenyl-1H-1,2,3-triazole-4-carboxamide: 866845-57-0
N-(4-chlorophenyl)-5-methyl-1-phenyl-1H-1,2,3-triazole-4-carboxamide

Guidance literature:: With iron(II) chloride; In N,N-dimethyl-formamide; at 80 ℃; for 10h; regiospecific reaction;
DOI:10.1039/c2cc33157h

Reference yield:

: 101-92-8
4'-Chloroacetoacetanilide

N-(4-chlorophenyl)-5-methyl-1-phenyl-1H-1,2,3-triazole-4-carboxamide: 866845-57-0
N-(4-chlorophenyl)-5-methyl-1-phenyl-1H-1,2,3-triazole-4-carboxamide

Guidance literature:: Multi-step reaction with 2 steps

1: 4-toluenesulfonyl azide; triethylamine / acetonitrile / 12 h / 20 °C

2: iron(II) chloride / N,N-dimethyl-formamide / 10 h / 80 °C

With 4-toluenesulfonyl azide; triethylamine; iron(II) chloride; In N,N-dimethyl-formamide; acetonitrile; 2: Wolff cyclocondensation;
DOI:10.1039/c2cc33157h