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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 398462Generated: October 26, 2026

Oxalyl chloride → {2-[2-(3-Chloro-phenyl)-3-cyclopentyl-propionylamino]-thiazol-4-yl}-acetic acid ethyl ester

https://huagongshe.com/reaction/398462

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-Thiazoleacetic acid, 2-amino-, ethyl esterHCID 104454—
Reactant2-(3-Chloro-phenyl)-3-cyclopentyl-propionic acidHCID 22315321—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product{2-[2-(3-Chloro-phenyl)-3-cyclopentyl-propionylamino]-thiazol-4-yl}-acetic acid ethyl esterHCID 2339457260.3%

Reaction Conditions

Temperature25 °C

Reaction Steps

A solution of 2-(3-chloro-phenyl)-3-cyclopentyl-propionic acid (252 mg, 1.0 mmol) in methylene chloride (10 mL) was cooled to 0° C. and then treated with a 2.0M solution oxalyl chloride in methylene chloride (0.6 mL, 1.2 mmol) and a few drops of N,N-dimethylformamide. The reaction mixture was stirred at 0° C. for 15 min and at 25° C. for 2 h. The reaction mixture was then treated with (2-amino-thiazol-4-yl)-acetic acid ethyl ester (409 mg, 2.2 mmol) and N,N-diisopropylethylamine (0.5 mL, 2.4 mmol). This solution was stirred at 25° C. for 48 h. At this time, the reaction was concentrated in vacuo. Flash chromatography (Merck Silica gel 60, 230-400 mesh, 80/20 hexanes/ethyl acetate) afforded {2-[2-(3-chloro-phenyl)-3-cyclopentyl-propionylamino]-thiazol-4-yl}-acetic acid ethyl ester (254 mg, 60.3%) as a white solid: mp 121-125° C.; EI-HRMS m/e calcd for C2 H25ClN2O3S (M+) 420.1274, found 420.1268.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06610846B1
Source datasetuspto-grants-2003_08
ORD IDord-dbdd0bcbb0164acea8fbad0024973bbd
Source noteuspto-grants-2003_08