4-Chloro-N-(4-chloro-benzoyl)-N-(5-methyl-4-phenyl-[1,2,3]triazol-1-yl)-benzamide

Base Information

Chemical Name:4-Chloro-N-(4-chloro-benzoyl)-N-(5-methyl-4-phenyl-[1,2,3]triazol-1-yl)-benzamide
CAS No.:98610-65-2
Molecular Formula:C₂₃H₁₆Cl₂N₄O₂
Molecular Weight:451.312
Hs Code.:

Synonyms:4-Chloro-N-(4-chloro-benzoyl)-N-(5-methyl-4-phenyl-[1,2,3]triazol-1-yl)-benzamide

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Chemical Property of 4-Chloro-N-(4-chloro-benzoyl)-N-(5-methyl-4-phenyl-[1,2,3]triazol-1-yl)-benzamide

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Technology Process of 4-Chloro-N-(4-chloro-benzoyl)-N-(5-methyl-4-phenyl-[1,2,3]triazol-1-yl)-benzamide

There total 1 articles about 4-Chloro-N-(4-chloro-benzoyl)-N-(5-methyl-4-phenyl-[1,2,3]triazol-1-yl)-benzamide 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:

: 94420-91-4
4-chloro-benzoic 4-chloro-N-(5-methyl-4-phenyl-[1,2,3]triazol-1-yl)-benzimidic anhydride

: 98610-65-2
4-Chloro-N-(4-chloro-benzoyl)-N-(5-methyl-4-phenyl-[1,2,3]triazol-1-yl)-benzamide

Guidance literature:: for 1h; Yield given; Heating;
DOI:10.1002/mrc.1260230720

Reference yield: 85.0%

: 98610-65-2
4-Chloro-N-(4-chloro-benzoyl)-N-(5-methyl-4-phenyl-[1,2,3]triazol-1-yl)-benzamide

: 98610-72-1
N-(5-Bromomethyl-4-phenyl-[1,2,3]triazol-1-yl)-4-chloro-N-(4-chloro-benzoyl)-benzamide

Guidance literature:: With N-Bromosuccinimide; dibenzoyl peroxide; In tetrachloromethane; for 6h; Heating;
DOI:10.1039/P19850001167

Reference yield:

: 98610-65-2
4-Chloro-N-(4-chloro-benzoyl)-N-(5-methyl-4-phenyl-[1,2,3]triazol-1-yl)-benzamide

: 98610-79-8
4H-6-p-chlorophenyl-3-phenyl-v-triazolo<1,5-d><1,3,4>oxadiazine

Guidance literature:: Multi-step reaction with 2 steps

1: 85 percent / N-bromosuccinimide, dibenzoyl peroxide / CCl₄ / 6 h / Heating

2: 24 percent / K₂CO₃ / 1,2,3,4-tetrahydro-naphthalene / 0.83 h / 180 °C

With N-Bromosuccinimide; potassium carbonate; dibenzoyl peroxide; In tetrachloromethane; tetralin;
DOI:10.1039/P19850001167