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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2296953Generated: October 31, 2026

2,2,2-Trifluoroethanesulfonyl chloride → 3-cyclopentyl-N-thiazol-2-yl-2-[4-(2,2,2-trifluoro-ethanesulfonylamino)-phenyl]-propionamide

https://huagongshe.com/reaction/2296953

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,2,2-Trifluoroethanesulfonyl chlorideHCID 74242—
Reactant2-(4-amino-phenyl)-3-cyclopentyl-N-thiazol-2-yl-propionamideHCID 9948802—
SolventPyridineHCID 1049—
Product3-cyclopentyl-N-thiazol-2-yl-2-[4-(2,2,2-trifluoro-ethanesulfonylamino)-phenyl]-propionamideHCID 1027641042.5%

Reaction Conditions

Temperature25 °C

Reaction Steps

A solution of 2-(4-amino-phenyl)-3-cyclopentyl-N-thiazol-2-yl-propionamide (prepared in Example 3, 158 mg, 0.5 mmol) in pyridine (5 mL) at 25° C. was treated with 2,2,2-trifluoroethanesulfonyl chloride (63.5 μL, 0.57 mmol). The reaction was stirred at 25° C. for 48 h and was then concentrated in vacuo. High pressure liquid chromatography (Chromegasphere SI-60, 10 μM, 60 Å, 25 cm×23 cm ID, 40/60 heptane/ethyl acetate) afforded the 3-cyclopentyl-N-thiazol-2-yl-2-[4-(2,2,2-trifluoro-ethanesulfonylamino)-phenyl]-propionamide (98.1 mg, 42.4%) as a light yellow oil: EI-HRMS m/e calcd for C19H22F3N3O3S2 (M+) 461.1054, found 461.1064.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06489485B2
Source datasetuspto-grants-2002_12
ORD IDord-4ce0032dfcb840b4bd0b920dd4584973
Source noteuspto-grants-2002_12