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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 331086Generated: October 30, 2026

Sodium borohydride → HCID 68179150, compound

https://huagongshe.com/reaction/331086

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 88860782HCID 88860782—
SolventMethanolHCID 887—
ProductHCID 68179150HCID 6817915097%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of tert-butyl(3R)-3-((R)-1-((S)-4-(4-chlorophenyl)-4-hydroxy-3,3-dimethylpiperidin-1-yl)-3-methyl-1-oxobutan-2-ylcarbamoyl)-1-(2-oxoethyl)cyclopentylcarbamate (from step D, 60 mg, 0.101 mmol) in MeOH (2 mL) at −78° C. was added NaBH4 (7.67 mg, 0.203 mmol). The resulting mixture was stirred at −78° C. for 1 hour. The solvent was removed under reduced pressure and to the residue was added ethyl acetate (10 mL). The resulting mixture was washed with water (2 mL), brine (2 mL), dried over Na2SO4 and concentrated to yield t-butyl(3R)-3-((R)-1-((S)-4-(4-chlorophenyl)-4-hydroxy-3,3-dimethylpiperidin-1-yl)-3-methyl-1-oxobutan-2-ylcarbamoyl)-1-(2-hydroxyethyl)cyclopentylcarbamate (58 mg, 0.098 mmol, 96% yield) as a solid. MS (ESI+) m/z 594 M+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08877749B2
Source datasetuspto-grants-2014_11
ORD IDord-b6df0e04f6434bf196bc293e90a9c884
Source noteuspto-grants-2014_11