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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 985545Generated: October 29, 2026

Sodium borohydride → 3'-(7-Hydroxymethylimidazo[1,2-alpha]-pyridin3-yl)biphenyl-2-carbonitrile

https://huagongshe.com/reaction/985545

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant3'-(7-Formylimidazo[1,2-alpha]pyridin-3-yl)biphenyl-2-carbonitrileHCID 9858378—
SolventMethanolHCID 887—
SolventChloroformHCID 6212—
Product3'-(7-Hydroxymethylimidazo[1,2-alpha]-pyridin3-yl)biphenyl-2-carbonitrileHCID 988035675.8%

Reaction Steps

3′-(7-Formylimidazo[1,2-α]pyridin-3-yl)biphenyl-2-carbonitrile (140 mg, 0.43 mmol) was suspended in chloroform (4 ml) and methanol (7 ml), sodium borohydride (82 mg, 2.17 mmol) added portionwise over 5 min then the reaction was heated under reflux for 1.5 h. The mixture was evaporated to dryness, the residue diluted with water (40 ml) and extracted with chloroform (2×50 ml). The combined organics were washed with brine (40 ml), dried over anhydrous sodium sulfate and evaporated to dryness. Purification was effected by silica gel chromatography eluting with dichloromethane and 1% conc. ammonia on a gradient of methanol (1-5%). The solid obtained was triturated with diethyl ether which gave the title compound (106 mg, 75%) as a white powder. 1H NMR (400 MHz, MeOD) δH 4.70 (2H, d, J 1), 6.97 (1H, dd, J 7 and 2), 7.55-7.60 (2H, m), 7.61-7.65 (1H, m), 7.67-7.80 (5H, m), 7.84-7.88 (2H, m), 8.65 (1H, dd, J 7 and 1); m/z (ES+) 326 (M++H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06872731B2
Source datasetuspto-grants-2005_03
ORD IDord-24199e1bde60479b8b7f22ff90089692
Source noteuspto-grants-2005_03