Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 19672Generated: October 25, 2026

2-Amino-5-chlorobenzophenone → N-(2-benzoyl-4-chlorophenyl)-1H-imidazole-1-carboxamide

https://huagongshe.com/reaction/19672

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-5-chlorobenzophenoneHCID 12870—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
SolventDichloromethaneHCID 6344—
ProductN-(2-benzoyl-4-chlorophenyl)-1H-imidazole-1-carboxamideHCID 2175527669.9%

Reaction Conditions

Temperature45 °C

Reaction Steps

To a solution of 2-amino-5-chlorobenzophenone (40 g, 172.7 mmol) in CH2Cl2 (175 μL) was added carbonyldiimidazole (30.8 g, 189.9 mmol). The reaction was heated to 45° C. for 16 h resulting in a white precipitate. The reaction was cooled in an ice bath and the precipitate collected by vacuum filtration and dried to give 39.3 g (69.9%) of N-(2-benzoyl-4-chlorophenyl)-1H-imidazole-1-carboxamide as a white solid. 1H NMR (CDCl3, 400 MHz) 8.66 (s, 1H); 7.46 (m, 4H); 7.25 (s, 1H); 7.19 (d, J=6.96 Hz, 2H); 7.15 (s, 1H); 6.94 (m, 2H); 6.76 (d, J=2.29 Hz, 1H). MS (Electrospray): m/z 348.0 (M+Na).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07745452B2
Source datasetuspto-grants-2010_06
ORD IDord-89b47f21b7964839ac20d179765c75c8
Source noteuspto-grants-2010_06