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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 986663Generated: October 30, 2026

4-Aminopyridine → HCID 70381943, compound

https://huagongshe.com/reaction/986663

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-AminopyridineHCID 1727—
Reactant2-ChloromethylbenzimidazoleHCID 78571—
SolventEthanolHCID 702—
ProductHCID 70381943HCID 70381943113.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 1.665 g (10 m mol) of 2- chloromethybenzimidazole and 1.88 g (20 m mol) of 4- aminopyridine in 20 ml of ethanol was refluxed under heating for three hours. The solution was evaporated in vacuo to a dark oil, dissolved in 20 ml of water and washed twice with 20 ml of ethylacetate The aqueous phase was evaporated in vacuo. The residual oil was dissolved in 3 ml of concentrated hydrochloric acid and chilled (0° C.) causing a crystalline precipitate to form. The crystals were filtered with the aid of ethanol. Recrystallization from methanol gave 1.68 g (53.3%) of the title compound (I).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04714764
Source datasetuspto-grants-1987_12
ORD IDord-07c970f2191141729624b113c9814452
Source noteuspto-grants-1987_12