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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 966564Generated: October 26, 2026

Methanol → 1-[2-(4-Chloro-phenyl)-3-cyclopentyl-propionyl]-3-methyl-urea

https://huagongshe.com/reaction/966564

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantMethylureaHCID 11719—
ReactantMethanol, magnesium salt (2:1)HCID 164537—
Reactant2-(4-Chloro-phenyl)-3-cyclopentyl-propionic acid ethyl esterHCID 46221154—
Product1-[2-(4-Chloro-phenyl)-3-cyclopentyl-propionyl]-3-methyl-ureaHCID 120444535.8%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 2-(4-chloro-phenyl)-3-cyclopentyl-propionic acid ethyl ester (1.65 g, 5.89 mmol) and methyl urea (654 mg, 8.83 mmol) in a solution of magnesium methoxide in methanol (7.4 wt %, 16.9 mL, 11.78 mmol) was heated under reflux at 100° C. for 6 h. The reaction mixture was then concentrated in vacuo. Flash chromatography (Merck Silica gel 60, 230-400 mesh, 75/25 hexanes/ethyl acetate) afforded 1-[2-(4-chloro-phenyl)-3-cyclopentyl-propionyl]-3-methyl-urea (105.3 mg, 5.8%) as a white solid: mp 145-147° C.; EI-HRMS m/e calcd for C16H21ClN2O2 (M+) 308.1292, found 308.1291. The methyl ester of the starting material was recovered from the reaction mixture due to transesterification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06951945B2
Source datasetuspto-grants-2005_10
ORD IDord-4582eea13be7444ea615f2ab72e57414
Source noteuspto-grants-2005_10