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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2050313Generated: October 31, 2026

Urea → 1-{3-[4-(diphenylmethyl)-1-piperazinyl]propyl}-1,3-dihydro-5-(trifluoromethyl)-2H-benzimidazol-2-one

https://huagongshe.com/reaction/2050313

Reaction equation

Participants

RoleNameHCIDCharge
ReactantUreaHCID 1176—
ReactantChloroformHCID 6212—
ReactantN1-{3-[4-(diphenylmethyl)-1-piperazinyl]propyl}-4-(trifluoromethyl)-1,2-benzenediamineHCID 86736963—
SolventWaterHCID 962—
Product1-{3-[4-(diphenylmethyl)-1-piperazinyl]propyl}-1,3-dihydro-5-(trifluoromethyl)-2H-benzimidazol-2-oneHCID 13105581—

Reaction Conditions

Temperature190 °C

Reaction Steps

A mixture of 5.4 parts of urea and 13.7 parts of N1 -{3-[4-(diphenylmethyl)-1-piperazinyl]propyl}-4-(trifluoromethyl)-1,2-benzenediamine is stirred and heated for 4 hours at 190° C. The reaction mixture is cooled to room temperature and diluted with water. After the addition of trichloromethane, the layers are separated. The aqueous phase is extracted with trichloromethane. The combined organic phases are washed with water, dried, filtered and evaporated. The oily residue is purified by column-chromatography over silica gel using trichloromethane and methanol (90:10 by volume) as eluent. The pure fractions are collected and the eluent is evaporated. The residue is crystallized from 2,2'-oxybispropane. The product is filtered off and dried, yielding 1-{3-[4-(diphenylmethyl)-1-piperazinyl]propyl}-1,3-dihydro-5-(trifluoromethyl)-2H-benzimidazol-2-one; mp. 152.7° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04200641
Source datasetuspto-grants-1980_04
ORD IDord-6b9fbe3ca346444ea1ee726016a2c7f4
Source noteuspto-grants-1980_04