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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1860132Generated: October 26, 2026

Methanol → 1-[3-Cyclopentyl-2-(4-trifluoromethanesulfonyl-phenyl)-propionyl]-3-methyl urea

https://huagongshe.com/reaction/1860132

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantMethylureaHCID 11719—
ReactantMethanol, magnesium salt (2:1)HCID 164537—
Reactant3-Cyclopentyl-2-(4-trifluoromethanesulfonyl-phenyl)propionic acid methyl esterHCID 46221384—
Product1-[3-Cyclopentyl-2-(4-trifluoromethanesulfonyl-phenyl)-propionyl]-3-methyl ureaHCID 1204445828%

Reaction Conditions

Temperature25 °C

Reaction Steps

3-Cyclopentyl-2-(4-trifluoromethanesulfonyl-phenyl)propionic acid methyl ester (383.8 mg, 1.05 mmol) and methyl urea (234.1 mg, 3.16 mmol) were treated with a solution of magnesium methoxide in methanol (7.4 wt %, 6.0 mL, 4.21 mmol). The resulting reaction mixture was then heated under reflux for 2 d. The reaction mixture was allowed to cool to 25° C. and then filtered through celite. The celite was thoroughly washed with ethyl acetate until the solvent passing through the celite showed absence of desired product by thin layer chromatography. The filtrate was concentrated in vacuo. Flash chromatography (Merck Silica gel 60, 70-230 mesh, 3/1 hexanes/ethyl acetate) afforded 1-[3-cyclopentyl-2-(4-trifluoromethanesulfonyl-phenyl)-propionyl]-3-methyl urea (119.3 mg, 28%) as a white solid: mp 191-192° C.; FAB-HRMS m/e calcd for C17H21F3N2O4S (M+H)+407.1252, found 407.1247.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06528543B1
Source datasetuspto-grants-2003_03
ORD IDord-c68c0cf50e194f10b93f6ccf32e22162
Source noteuspto-grants-2003_03