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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1506244Generated: October 31, 2026

Sodium borohydride → HCID 58078505, compound

https://huagongshe.com/reaction/1506244

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 58078489HCID 58078489—
SolventMethanolHCID 887—
ProductHCID 58078505HCID 5807850589.2%

Reaction Steps

4-[(1-Benzylpiperidin-4-yl)amino]-1-{[2-(trimethylsilyl)ethoxy]methyl}-1H-pyrrolo[2,3-b]pyridine-5-carbaldehyde (289 mg, 0.620 mmol) in methanol was stirred with sodium borohydride (35.3 mg, 0.93 mmol) at room temperature for 1 hour. The reaction mixture was concentrated under reduced pressure and, after addition of water, extracted with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate=1/1 (v/v)) to give the title compound (258 mg, yield 89%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09216999B2
Source datasetuspto-grants-2015_12
ORD IDord-6ea8a2474f3f46ffadeb23e158dff68c
Source noteuspto-grants-2015_12