Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1924321Generated: October 28, 2026

Sodium borohydride → HCID 57742987, compound

https://huagongshe.com/reaction/1924321

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 numberUS08178533B2
Source datasetuspto-grants-2012_05
ORD IDord-1714b3d3e1f24c01ab5296e11925c40f
Source noteuspto-grants-2012_05