3-Imidazol-1-yl-2-oxo-3-phenyl-2,3-dihydro-indole-1-carboxylic acid phenylamide

Base Information

Chemical Name:3-Imidazol-1-yl-2-oxo-3-phenyl-2,3-dihydro-indole-1-carboxylic acid phenylamide
CAS No.:79419-85-5
Molecular Formula:C₂₄H₁₈N₄O₂
Molecular Weight:394.433
Hs Code.:

Synonyms:3-Imidazol-1-yl-2-oxo-3-phenyl-2,3-dihydro-indole-1-carboxylic acid phenylamide

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Chemical Property of 3-Imidazol-1-yl-2-oxo-3-phenyl-2,3-dihydro-indole-1-carboxylic acid phenylamide

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Technology Process of 3-Imidazol-1-yl-2-oxo-3-phenyl-2,3-dihydro-indole-1-carboxylic acid phenylamide

There total 4 articles about 3-Imidazol-1-yl-2-oxo-3-phenyl-2,3-dihydro-indole-1-carboxylic acid phenylamide 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: 68.0%

: 103-71-9
phenyl isocyanate

: 77014-60-9
3-Imidazol-1-yl-3-phenyl-1,3-dihydro-indol-2-one

: 79419-85-5
3-Imidazol-1-yl-2-oxo-3-phenyl-2,3-dihydro-indole-1-carboxylic acid phenylamide

Guidance literature:: With triethylamine; In benzene; at 50 ℃; for 0.333333h;

Reference yield:

: 108-86-1,52753-63-6
bromobenzene

: 79419-85-5
3-Imidazol-1-yl-2-oxo-3-phenyl-2,3-dihydro-indole-1-carboxylic acid phenylamide

Guidance literature:: Multi-step reaction with 3 steps

1: 1.) Mg / 1.) THF; 2.) r.t., 1 h

2: 1.) SOCl₂ / 1.) CH₂Cl₂, 30 min; 2.) CH₂Cl₂, 75 min

3: 68 percent / Et₃N / benzene / 0.33 h / 50 °C

With thionyl chloride; magnesium; triethylamine; In benzene;

Reference yield:

: 139018-14-7,1848-24-4
3-hydroxy-3-phenyl-1,3-dihydro-indol-2-one

: 79419-85-5
3-Imidazol-1-yl-2-oxo-3-phenyl-2,3-dihydro-indole-1-carboxylic acid phenylamide

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) SOCl₂ / 1.) CH₂Cl₂, 30 min; 2.) CH₂Cl₂, 75 min

2: 68 percent / Et₃N / benzene / 0.33 h / 50 °C

With thionyl chloride; triethylamine; In benzene;