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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1173278Generated: November 2, 2026

tert-butyl N-(4-oxocyclohexyl)carbamate → HCID 58751594, compound

https://huagongshe.com/reaction/1173278

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-butyl N-(4-oxocyclohexyl)carbamateHCID 1512535—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant(R)-N-(2-oxo-2-(pyrrolidin-3-ylamino)ethyl)-3-(trifluoromethyl)benzamideHCID 59556069—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58751594HCID 5875159445%

Reaction Steps

To a solution of the ketone of step A (0.4 g, 1.9 mmol) and the pyrrolidine intermediate obtained in step C, Example 114 (0.4 g, 1.3 mmol) in THF (15 mL) was added sodium triacetoxyborohydride (0.4 g, 1.9 mmol). The reaction was stirred at room temperature overnight and quenched by addition of aqueous NaHCO3. The resulting solution was extracted with EtOAc three times. The combined organic phase was washed with with NaHCO3 and brine, dried over MgSO4 and concentrated. Flash chromatography eluting with a gradient of 0-20% MeOH/CH2Cl2 provided 300 mg of the title compound. MS calculated (M+H)+ 513, found 513.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07834021B2
Source datasetuspto-grants-2010_11
ORD IDord-d203a43f449f4ab199a3c212ee74e43c
Source noteuspto-grants-2010_11