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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 430205Generated: October 29, 2026

Triphenylphosphine → HCID 20707085, compound

https://huagongshe.com/reaction/430205

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantN-bromobutanimideHCID 67184—
Reactant4-Thiazoleacetic acid, 2-amino-, ethyl esterHCID 104454—
Reactant3-Cyclopentyl-2-(4-trifluoromethanesulfonyl-phenyl)propionic acidHCID 22315092—
SolventDichloromethaneHCID 6344—
ProductHCID 20707085HCID 2070708572.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of triphenylphosphine (97 mg, 0.371 mmol) in methylene chloride (1.5 mL) was cooled to 0° C. and then slowly treated with N-bromosuccinimide (66 mg, 0.371 mmol). The reaction mixture was stirred at 0° C. for 20 min and then treated with 3-cyclopentyl-2-(4-trifluoromethanesulfonyl-phenyl)propionic acid (100 mg, 0.285 mmol). The resulting reaction mixture was stirred at 0° C. for 10 min, allowed to warm to 25° C., and then treated with ethyl 2-amino-4-thiazoleacetate (123 mg, 0.657 mmol). The resulting reaction mixture was stirred at 25° C. for 3 d. The reaction mixture was then concentrated in vacuo. Flash chromatography (Merck Silica gel 60, 230-400 mesh, 3/1 hexanes/ethyl acetate) afforded {2-[3-cyclopentyl-2-(4-trifluoromethanesulfonyl-phenyl)-propionyl-amino]-thiazol-4-yl}-acetic acid ethyl ester (107 mg, 72%) as a yellow foam: mp 48-51° C.; EI-HRMS m/e calcd for C22H25F3N2O5S2 (M+) 518.1157, found 518.1157.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06320050B1
Source datasetuspto-grants-2001_11
ORD IDord-d9d898751f9d4516a4b544a1c35af0d9
Source noteuspto-grants-2001_11