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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1386056Generated: November 2, 2026

Sodium Hydroxide → 2,3-Dimethyl-8-(2,6-diethylbenzylamino)-imidazo[1,2-a]pyridine

https://huagongshe.com/reaction/1386056

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant2,6-DiethylbenzaldehydeHCID 13184778—
Reactant2,3-Dimethylimidazo[1,2-a]pyridin-8-amineHCID 21873980—
CatalystZincchlorideHCID 3007855—
SolventMethanolHCID 887—
SolventHexaneHCID 8058—
Product2,3-Dimethyl-8-(2,6-diethylbenzylamino)-imidazo[1,2-a]pyridineHCID 21717350—

Reaction Steps

8-amino-2,3-dimethyl-imidazo[1,2-a]pyridine (0.33 g, 2.0 mmol) and 2,6-diethylbenzaldehyde (0.36 g, 2.2 mmol) were dissolved in methanol (7 ml). ZnCl2 (0.30 g, 2.2 mmol) and subsequently NaBH3CN (0.14 g, 2.2 mmol) in small portions were added and the mixture was refluxed under argon for 3 hours, cooled and then poured over an aqueous 1M NaOH solution (10 ml). The resultant yellow suspension was extracted with DCM (3×25 ml) and the combined organic solutions were washed with brine, dried over Na2SO4 and then removed. The oily residue (0.4 g) was purified by flash chromatography (DCM-EtOAc 0%-20% EtOAc) to give 0.34 g. Treatment of this oily product with hexane (2 ml) afforded 0.14 g (23%) as off-white crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06265415B1
Source datasetuspto-grants-2001_07
ORD IDord-754303612eb64590bcff75744c3659ab
Source noteuspto-grants-2001_07