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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1173262Generated: October 30, 2026

Water → N-[2-({(3R)-1-[4-Fluoro-4-(1,3-thiazol-2-yl)cyclohexyl]pyrrolidin-3-yl}amino)-2-oxoethyl]-3-(trifluoromethyl)benzamide

https://huagongshe.com/reaction/1173262

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEthyl AcetateHCID 8857—
Reactant(Diethylamino)sulfur trifluorideHCID 123472—
ReactantN-[2-({(3R)-1-[4-Hydroxy-4-(1,3-thiazol-2-yl)cyclohexyl]pyrrolidin-3-yl}amino)-2-oxoethyl]-3-(trifluoromethyl)benzamideHCID 58751593—
SolventDichloromethaneHCID 6344—
ProductN-[2-({(3R)-1-[4-Fluoro-4-(1,3-thiazol-2-yl)cyclohexyl]pyrrolidin-3-yl}amino)-2-oxoethyl]-3-(trifluoromethyl)benzamideHCID 6678713933.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

DAST (0.2 mL, 1.5 mmol) was added to N-[2-({(3R)-1-[4-hydroxy-4-(1,3-thiazol-2-yl)cyclohexyl]pyrrolidin-3-yl}amino)-2-oxoethyl]-3-(trifluoromethyl)benzamide (0.06 g, 0.12 mmol) in CH2Cl2 (5 mL) at −78° C. with stirring under N2. The solution was allowed to warm to 0° C. slowly and stirred for 1 h. Water and EtOAc were added. The aqueous layer was extracted with EtOAc (3×). The combined organic layers were washed with saturated NaCl, dried (MgSO4), concentrated and purified by flash chromatography and reverse-phase HPLC to give 0.020 g of the title compound in 31% yield. MS (EI) calcd: (M+H)+=499.2; found: 499.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07834021B2
Source datasetuspto-grants-2010_11
ORD IDord-e1e5583d62964d0daa744ddcb2e8c4ab
Source noteuspto-grants-2010_11