Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2043681Generated: November 2, 2026

Sodium borohydride → HCID 57742987, compound

https://huagongshe.com/reaction/2043681

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 57743086HCID 57743086—
SolventEthanolHCID 702—
ProductHCID 57742987HCID 5774298765%

Reaction Steps

Methyl 6-bromo-3-(4-methoxybenzyl)-3H-imidazo[4,5-b]pyridine-7-carboxylate x210 (1.2 g, 3.19 mmol) is dissolved in absolute ethanol. NaBH4 (0.36 g, 3 eq, 9.57 mmol) is added at 5° C. under stirring. The cooling bath is removed after 4 h, and the reaction mixture is allowed to heat up to room temperature. The stirring is continued at this temperature for 20 h. The reaction mixture is evaporated in the vacuum of a rotary evaporator at 35° C., and the residue is partitioned in ethyl acetate/saturated aqueous NaHCO3 mixture. The organic layer is dried with anhydrous sodium sulfate and evaporated. The crude product is purified by chromatography on silicagel (dichloromethane/methanol) to afford 0.72 g of [6-bromo-3-(4-methoxybenzyl)-3H-imidazo[4,5-b]pyridin-7-yl]methanol x211.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08586623B2
Source datasetuspto-grants-2013_11
ORD IDord-8fb037eb548e41c893dcc42e39661609
Source noteuspto-grants-2013_11