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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1386071Generated: October 27, 2026

Sodium cyanoborohydride → HCID 21717362, compound

https://huagongshe.com/reaction/1386071

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 22672632HCID 22672632—
Reactant2-Ethyl-6-methylbenzaldehydeHCID 22997469—
CatalystZincchlorideHCID 3007855—
SolventMethanolHCID 887—
ProductHCID 21717362HCID 2171736233%

Reaction Steps

A stirred mixture of 8-amino-2,3,6-trimethylimidazo[1,2-a]pyridine (0.5 g, 2.8 mmol), 2-ethyl-6-methylbenzaldehyde (0.45 g, 3 mmol) and zinc(II)chloride (0.4 g, 3 mmol) in 50 ml methanol was treated with sodium cyanoborohydride (0.19 g, 3 mmol) and refluxed for 20 h. The methanol was evaporated under reduced pressure and the residue was dissolved in dichloromethylene and water. The organic layer was separated, dried over sodium sulfate and evaporated under reduced pressure. The residue was chromatographed on silicagel with dichloromethylene:methanol (10:1) which yielded 0.28 g (33%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06265415B1
Source datasetuspto-grants-2001_07
ORD IDord-d0cff468a59141b48036f99aff1afe30
Source noteuspto-grants-2001_07