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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1836402Generated: October 30, 2026

Phenyl isocyanate → 4-[3-(Phenylureido)benzoyl]-1-methylpiperidine

https://huagongshe.com/reaction/1836402

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenyl isocyanateHCID 7672—
Reactant4-[3-Aminobenzoyl]-1-methylpiperidineHCID 10130651—
SolventAcetic AcidHCID 176—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
Product4-[3-(Phenylureido)benzoyl]-1-methylpiperidineHCID 2349932974%

Reaction Steps

4-[3-aminobenzoyl]-1-methylpiperidine (25 mg, 0.115 mmol) and phenyl isocyanate (37 μL, 0.344 mmol) in methylene chloride (2 mL) were mixed for 72 h at ambient temperature. The solution was diluted with 10% acetic acid in methanol and poured over a Varian Mega Bond Elut™ strong cation exchange column. The column was rinsed extensively with methanol to remove impurities, then treated with a 2M ammonia in methanol to elute the product from the column. The solvent was evaporated and the residue was stirred with 5N sodium hydroxide solution (1 mL). The solvent was removed under vacuum and the residue was purified by silica gel chromatography (methylene chloride:methanol:ammonium hydroxide, 97.5:2.5:0.25 then 95:5:0.5). The solvent was evaporated to give 28.5 mg (74%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06777428B1
Source datasetuspto-grants-2004_08
ORD IDord-e6247230952442b8916308b1af3aa6b6
Source noteuspto-grants-2004_08