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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1386070Generated: November 1, 2026

Sodium cyanoborohydride → HCID 17872261, compound

https://huagongshe.com/reaction/1386070

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant2,6-DiethylbenzaldehydeHCID 13184778—
Reactant8-Amino-2,3,6-trimethylimidazo[1,2-a]pyridineHCID 22672632—
CatalystZincchlorideHCID 3007855—
SolventMethanolHCID 887—
ProductHCID 17872261HCID 1787226146.7%

Reaction Steps

A stirred mixture of 8-amino-2,3,6-trimethylimidazo[1,2-a]pyridine (0.5 g, 2.8 mmol), 2,6-diethylbenzaldehyde (0.7 g, 4.3 mmol) and zinc(II)chloride (0.44 g, 3 mmol) in 50 ml methanol was treated with sodium cyanoborohydride (0.19 g, 3 mmol) and then 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 silica gel with dichloromethylene first and then dichloromethylene:ethylacetate (1:1) which yielded 0.42 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06265415B1
Source datasetuspto-grants-2001_07
ORD IDord-f6d2bd4e985f4d658fd6b9b2ca12a52f
Source noteuspto-grants-2001_07