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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2088148Generated: November 1, 2026

Sodium borohydride → HCID 86586680, compound

https://huagongshe.com/reaction/2088148

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 86586679HCID 86586679—
SolventMethanolHCID 887—
ProductHCID 86586680HCID 8658668072.6%

Reaction Steps

Sodium borohydride (55 mg, 1.44 mmol) was added to a stirred solution of (1R*,2R*,5S*)-8-benzyl-2-{[3,5-bis(trifluoromethyl)phenyl]methoxy}-1-phenyl-8-azabicyclo[3.2.1]octan-6-one (Example 41; 50 mg 0.09 mmol) in methanol (3 ml) at +5° C. The reaction mixture was stirred for 15 minutes and quenched with saturated aqueous NaHCO3 and extracted into dichloromethane. The combined organic extracts were dried (Na2SO4) and concentrated. The residue was purified by chromatography on silica gel (iso-hexane:diethyl ether 10-45%) to give the title, compound (35 mg, 70%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06727249B2
Source datasetuspto-grants-2004_04
ORD IDord-c610a12a847a4b80b9984de19e608215
Source noteuspto-grants-2004_04