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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2088211Generated: November 2, 2026

Sodium borohydride → HCID 86586760, compound

https://huagongshe.com/reaction/2088211

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 86586761HCID 86586761—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86586760HCID 8658676095%

Reaction Steps

Sodium borohydride (13 mg, 0.34 mmol) was added to a solution of (1R*,2R*,5S*,6R*)-8-benzyl-2-{[3,5-bis(trifluoromethyl)phenyl]methoxy}-6-[2-(2-oxopropyl)-2H-tetrazol-5-yl]-1-phenyl-8-azabicyclo[3.2.1]octane (Compound 3i in Table 3; 0.2 g, 0.31 mmol) in methanol (10 ml) and THF (2 ml). The mixture was stirred at room temperature for 18 hours. The reaction mixture was concentrated in vacuo and the residue partitioned between saturated sodium hydrogen carbonate and ethyl acetate. The organic layer was separated, dried (MgSO4), filtered and concentrated. The residue was chromatographed on silica gel eluting with 25 and 35% ethyl acetate/iso-hexanes to yield the title compound (189 mg, 95%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06727249B2
Source datasetuspto-grants-2004_04
ORD IDord-d7437bb7ec83427b82f7c2fef638ea28
Source noteuspto-grants-2004_04