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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1369559Generated: October 27, 2026

Sodium Hydroxide → 8-(4-Methoxy-2,6-dimethylbenzylamino)-2,3-dimethylimidazo[1,2-a]pyridine

https://huagongshe.com/reaction/1369559

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant4-Methoxy-2,6-dimethylbenzaldehydeHCID 816779—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant2,3-Dimethylimidazo[1,2-a]pyridin-8-amineHCID 21873980—
CatalystZincchlorideHCID 3007855—
SolventMethanolHCID 887—
Product8-(4-Methoxy-2,6-dimethylbenzylamino)-2,3-dimethylimidazo[1,2-a]pyridineHCID 983964260.5%

Reaction Conditions

Temperature2.5 °C

Reaction Steps

8-amino-2,3-dimethylimidazo[1,2-a]pyridine (0.5 g, 3.1 mmol), 4-methoxy-2.6-dimethylbenzaldehyd (0.51 g, 3.11 mmol) were dissolved in methanol (10 ml) whereupon zinc chloride (0.51 g, 3.82 mmol) dissolved in methanol (5 ml) was added. Sodium cyanoborohydride was added in portions and the mixture was refluxed for 3 h under under nitrogen. The mixture was stirred at 0-5° C. and 1 M sodium hydroxide (20 ml) was added. After extraction with 2×50 ml of methylene chloride the combined organic layer was washed with water and dried over sodium sulfate. The solvent was removed under reduced pressure. The residue was chromatographed on silica (dichloromethane: ethyl acetate. 1:1) yielding 0.58 g 60% of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06579884B1
Source datasetuspto-grants-2003_06
ORD IDord-510b5e6461af464a9e5ca7953118173c
Source noteuspto-grants-2003_06