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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1389306Generated: October 30, 2026

Methane → HCID 54024057, compound

https://huagongshe.com/reaction/1389306

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethaneHCID 297—
ReactantUreaHCID 1176—
Reactant4-{[4-(Diphenylmethyl)piperazin-1-yl]methyl}-N~1~-methylbenzene-1,2-diamineHCID 3017879—
SolventHydrochloric AcidHCID 313—
SolventWaterHCID 962—
ProductHCID 54024057HCID 54024057—

Reaction Conditions

Temperature190 °C

Reaction Steps

A mixture of 4.64 parts of 4-[4-(diphenylmethyl)-1-piperazinylmethyl]-N1 -methyl-1,2-benzenediamine and 1.2 parts of urea is stirred and heated for 1.50 hours at 190° C. The reaction mixture is cooled and dissolved in a mixture of 150 parts of water and 6 parts of a hydrochloric acid solution 10 N. The solution is treated with activated charcoal. The latter is filtered off and the filtrate is alkalized with a sodium hydroxide solution 5 N. The product is extracted three times with dichloromethane. The combined extracts are dried, filtered and evaporated. The solid residue is stirred in 20 parts of ethanol. The product is filtered off and purified by column-chromatography over silica gel using a mixture of trichloromethane and methanol (97.5:2.5 by volume) as eluent. The pure fractions are collected and the eluent is evaporated. The solid residue is treated with 20 parts of ethanol. The product is filtered off, washed with a small amount of ethanol and dried, yielding 1.7 parts of 5-[ 4-(diphenylmethyl)-1-piperazinylmethyl]-1,3-dihydro-1-methyl-2H-benzimidazol-2-one; mp. 246° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04243806
Source datasetuspto-grants-1981_01
ORD IDord-7c4885e4eae34216bf420ebbc24e88f7
Source noteuspto-grants-1981_01