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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1729808Generated: November 1, 2026

Urea → HCID 21500249, compound

https://huagongshe.com/reaction/1729808

Reaction equation

Participants

RoleNameHCIDCharge
ReactantUreaHCID 1176—
ReactantHCID 21500251HCID 21500251—
SolventTolueneHCID 1140—
ProductHCID 21500249HCID 21500249—

Reaction Conditions

Temperature160 °C

Reaction Steps

A mixture of 36 parts of methyl 4-(2-amino-4-chlorophenylamino)-2-methyl-1-piperidinecarboxylate and 14 parts of urea is stirred and heated in an oil-bath at 160° C. for 4 hours. After cooling, the reaction mixture is disslved in methylbenzene. The solution is washed successively three times with water, twice with a diluted hydrochloric acid solution and again three times with water, dried, filtered and evaporated. The oily residue is purified by column-chromatography over silicagel, using trichloromethane as eluent. The pure fractions are collected and the eluent is evaporated, yielding methyl 4-(5-chloro-1,3-dihydro-2-oxo-2H-benzimidazol-1-yl)-2-methyl-1-piperidinecarboxylate as an oily residue.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03989707
Source datasetuspto-grants-1976_11
ORD IDord-864f4c2a6ee04fec9a415680487f5bfb
Source noteuspto-grants-1976_11