methyl-1-(3-trifluoromethylphenyl)methyl-5-diphenyl-acetyl-4,5,6,7-tetrahydro-1H-imidazo[4,5-c]pyridine-6-carboxylate

Base Information

Chemical Name:methyl-1-(3-trifluoromethylphenyl)methyl-5-diphenyl-acetyl-4,5,6,7-tetrahydro-1H-imidazo[4,5-c]pyridine-6-carboxylate
CAS No.:114786-28-6
Molecular Formula:C₃₀H₂₆F₃N₃O₃
Molecular Weight:533.55
Hs Code.:

Synonyms:methyl-1-(3-trifluoromethylphenyl)methyl-5-diphenyl-acetyl-4,5,6,7-tetrahydro-1H-imidazo[4,5-c]pyridine-6-carboxylate

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Chemical Property of methyl-1-(3-trifluoromethylphenyl)methyl-5-diphenyl-acetyl-4,5,6,7-tetrahydro-1H-imidazo[4,5-c]pyridine-6-carboxylate

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Technology Process of methyl-1-(3-trifluoromethylphenyl)methyl-5-diphenyl-acetyl-4,5,6,7-tetrahydro-1H-imidazo[4,5-c]pyridine-6-carboxylate

There total 4 articles about methyl-1-(3-trifluoromethylphenyl)methyl-5-diphenyl-acetyl-4,5,6,7-tetrahydro-1H-imidazo[4,5-c]pyridine-6-carboxylate 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:

: 114786-25-3
methyl-5-diphenylacetyl-3-(2-oxo-2-phenyl-ethyl)-4,5,6,7-tetrahydro-1 H-imidazo[4,5-c ]pyridine-6-carboxylate

: 497-19-8
sodium carbonate

: 705-29-3
3-Trifluoromethylbenzyl chloride

: 114786-28-6
methyl-1-(3-trifluoromethylphenyl)methyl-5-diphenyl-acetyl-4,5,6,7-tetrahydro-1H-imidazo[4,5-c]pyridine-6-carboxylate

Guidance literature:: With acetic acid; zinc; In methanol; dichloromethane; acetonitrile;

Reference yield:

: 117-34-0
2,2-diphenylacetic acid

: 114786-28-6
methyl-1-(3-trifluoromethylphenyl)methyl-5-diphenyl-acetyl-4,5,6,7-tetrahydro-1H-imidazo[4,5-c]pyridine-6-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: dicyclohexylcarbodiimide (DCC), hydroxybenztriazole (HOBT*H₂O) / dimethylformamide

2: 2.) glacial AcOH, Zn / 1.) CH₃CN, reflux, 2.) MeOH, sonication, 2 h

With benzotriazol-1-ol; acetic acid; dicyclohexyl-carbodiimide; zinc; In N,N-dimethyl-formamide;
DOI:10.1021/jm00115a014

Reference yield:

: (S)-3-(2-Oxo-2-phenyl-ethyl)-4,5,6,7-tetrahydro-3H-imidazo[4,5-c]pyridine-6-carboxylic acid methyl ester

: 114786-28-6
methyl-1-(3-trifluoromethylphenyl)methyl-5-diphenyl-acetyl-4,5,6,7-tetrahydro-1H-imidazo[4,5-c]pyridine-6-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: dicyclohexylcarbodiimide (DCC), hydroxybenztriazole (HOBT*H₂O) / dimethylformamide

2: 2.) glacial AcOH, Zn / 1.) CH₃CN, reflux, 2.) MeOH, sonication, 2 h

With benzotriazol-1-ol; acetic acid; dicyclohexyl-carbodiimide; zinc; In N,N-dimethyl-formamide;
DOI:10.1021/jm00115a014