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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 707356Generated: October 29, 2026

Sodium borohydride → HCID 89763461, compound

https://huagongshe.com/reaction/707356

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 89763770HCID 89763770—
SolventTetrahydrofuranHCID 8028—
ProductHCID 89763461HCID 89763461—

Reaction Steps

(1H-benzo[d]imidazol-2-yl)(3-(2-methoxy-3H-imidazo[4,5-b]pyridin-3-yl)cyclobutyl)methanone (60 mg, 0.17 mmol) was dissolved in dry tetrahydrofuran (10 mL) and treated with sodium borohydride (11 mg, 0.29 mmol). The reaction was stirred at room temperature until the starting material was consumed by TLC. After that, the reaction solution was concentrated under reduced pressure and the residue was purified by column chromatography on silica gel, followed by prep. TLC (dichloromethane:methanol=10:1) to give two isomers of (1H-benzo[d]imidazol-2-yl)-3-(2-methoxy-3H-imidazo[4,5-b]pyridin-3-yl)cyclobutyl)methanol as mixtures of diastereomers. M+1: 367.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09174992B2
Source datasetuspto-grants-2015_11
ORD IDord-81951b853e1a474f93a70780c5b5f7fe
Source noteuspto-grants-2015_11