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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1015979Generated: October 31, 2026

Triethylamine → n-(2-{[(9s)-7-(4-Hydroxy-4-phenylcyclohexyl)-1-oxa-7-azaspiro[4.4]non-9-yl]amino}-2-oxoethyl)-3-(trifluoromethyl)benzamide

https://huagongshe.com/reaction/1015979

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-Hydroxy-4-phenylcyclohexan-1-oneHCID 583741—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactantn-{2-[(9s)-1-Oxa-7-azaspiro[4.4]non-9-ylamino]-2-oxoethyl}-3-(trifluoromethyl)benzamideHCID 59556036—
SolventTetrahydrofuranHCID 8028—
Productn-(2-{[(9s)-7-(4-Hydroxy-4-phenylcyclohexyl)-1-oxa-7-azaspiro[4.4]non-9-yl]amino}-2-oxoethyl)-3-(trifluoromethyl)benzamideHCID 10098936—

Reaction Steps

To a solution of the amine of step H (90 mg, 0.243 mmol) and 4-hydroxy-4-phenyl-cyclohexanone (43 mg, 0.226 mmol) in THF (5 mL) was added sodium triacetoxyborohydride (129 mg, 0.61 mmol) followed by Et3N (0.29 ml, 21 mmol). The mixture was stirred at room temperature overnight. Solvent was removed under vacuum. The residue was taken up in EtOAc/NaHCO3 aqueous solution. The two phases were separated and the water layer was extracted with EtOAc twice. The combined organic phase was dried (Na2SO4) and concentrated. Purification by prep-HPLC provided two isomers. MS: 546.4 (M+1)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07985730B2
Source datasetuspto-grants-2011_07
ORD IDord-9e2b9b3574b24305afff83f8305937e1
Source noteuspto-grants-2011_07