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

HRID 1355000Notes

Reaction equation

HRID 1355000 reaction equation
C(O[C:4](=[O:19])[CH:5]([C:12]1[CH:17]=[CH:16][C:15]([Cl:18])=[CH:14][CH:13]=1)[CH2:6][CH:7]1[CH2:11][CH2:10][CH2:9][CH2:8]1)C.[CH3:20][NH:21][C:22]([NH2:24])=[O:23].C[O-].[Mg+2].C[O-].CO>>[Cl:18][C:15]1[CH:14]=[CH:13][C:12]([CH:5]([CH2:6][CH:7]2[CH2:8][CH2:9][CH2:10][CH2:11]2)[C:4]([NH:24][C:22]([NH:21][CH3:20])=[O:23])=[O:19])=[CH:17][CH:16]=1

Participants

5

Reactant 4

HCID 887MethanolHCID 11719MethylureaHCID 164537Methanol, magnesium salt (2:1)HCID 462211542-(4-Chloro-phenyl)-3-cyclopentyl-propionic acid ethyl ester

Product 1

HCID 120444531-[2-(4-Chloro-phenyl)-3-cyclopentyl-propionyl]-3-methyl-ureaYield 5.8%

Conditions

Temperature
100 °C

Procedure

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.

Workup

  1. temperaturewas heated
  2. concentrationThe reaction mixture was then concentrated in vacuo

Sources & evidence

ORD record
ord-3e5ed788f6294a0ca793cad0cf17d673
Source dataset
uspto-grants-2007_05
Patent number
US07223868B2

Reaction notes

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