Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1173290Generated: October 31, 2026

4-Hydroxy-4-phenylcyclohexan-1-one → N-(2-{[3-(Fluoromethyl)-1-(4-hydroxy-4-phenylcyclohexyl)pyrrolidin-3-yl]amino}-2-oxoethyl)-3-(trifluoromethyl)benzamide

https://huagongshe.com/reaction/1173290

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Hydroxy-4-phenylcyclohexan-1-oneHCID 583741—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantN-(2-{[3-(fluoromethyl)pyrrolidin-3-yl]amino}-2-oxoethyl)-3-(trifluoromethyl)benzamideHCID 59556164—
SolventDichloromethaneHCID 6344—
ProductN-(2-{[3-(Fluoromethyl)-1-(4-hydroxy-4-phenylcyclohexyl)pyrrolidin-3-yl]amino}-2-oxoethyl)-3-(trifluoromethyl)benzamideHCID 5955616716.7%

Reaction Steps

100 mg (0.53 mmol) of 4-hydroxy -4-phenylcyclohexanone and 184 mg (0.53 mmol) of N-(2-{[3-(fluoromethyl)pyrrolidin-3-yl]amino}-2-oxoethyl)-3-(trifluoromethyl)benzamide were dissolved in 10 mL of methylene chloride. To the solution was added 221 mg (1.06 mmol) of sodium triacetoxyborohydride. The reaction mixture was stirred at room temperature for 2 h. Direct chromatography on silica gel gave the final desired product 41 mg (top spot on TLC and first peak on HPLC, yield: 16.7%, MS: 522 (M+1)+) and the other isomer 51 mg (second peak on HPLC, yield: 20%, MS: 522 (M+1)+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07834021B2
Source datasetuspto-grants-2010_11
ORD IDord-dfbf3c2c76a24db29377447ea4150c83
Source noteuspto-grants-2010_11