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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1698248Generated: November 1, 2026

Sodium borohydride → HCID 59278380, compound

https://huagongshe.com/reaction/1698248

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 59278493HCID 59278493—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59278380HCID 59278380—

Reaction Steps

To a chilled (0° C.) solution of 1-(4-fluorophenyl)-1H-pyrazolo[3,4-c]pyridine-4-carboxylic acid [(S)-1-(2-formyl-pyridin-4-yl)-propyl]-amide (95 mg, 0.24 mmol) in THF (2 mL) and methanol (2 mL) was added sodium borohydride (17.8 mg, 0.47 mmol). The mixture was then warmed to room temperature. After 1.5 hours, the mixture was quenched with water (5 mL) and extracted with EtOAc (20 mL). The organic layer was washed with brine, dried over sodium sulfate, filtered and concentrated. The mixture was purified by silica gel chromatography eluting with a gradient of 0-10% methanol in dichloromethane to afford the title compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163918B2
Source datasetuspto-grants-2012_04
ORD IDord-c3bc6744bbb04d0392dcb92e84048951
Source noteuspto-grants-2012_04