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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 484606Generated: October 26, 2026

Pyridine → N-[4-(2-methyl-1H-imidazol-1-yl)phenyl]-4-(tetradecyloxy)benzeneacetamide

https://huagongshe.com/reaction/484606

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant4-(2-methyl-1H-imidazol-1-yl)anilineHCID 3157478—
Reactantp-TetradecyloxyphenylacetylchlorideHCID 10021844—
SolventTetrahydrofuranHCID 8028—
ProductN-[4-(2-methyl-1H-imidazol-1-yl)phenyl]-4-(tetradecyloxy)benzeneacetamideHCID 1503016258.3%

Reaction Steps

To a solution of 5.0 g of p-tetradecyloxyphenylacetyl chloride in 50 ml of tetrahydrofuran is added to a solution of 4.31 g of pyridine and 2.36 g of 4-(2-methyl-1H-imidazol-1-yl)benzenamine in 50 ml of tetrahydrofuran over 5 minutes. The mixture is stirred at ambient temperature for 1 hour, heated to reflux and allowed to stir at room temperature for 2 hours. The solvent is evaporated to a residue which is partitioned between chloroform and dilute sodium bicarbonate. The organic layer is separated, washed with water, dried and filtered through a pad of magnesium silicate. The solvent is evaporated to an oil which crystallizes from methyl alcohol:water to give 4.0 g of white solid which is chromatographed on silica gel using ethyl acetate containing 0.1% ammonium hydroxide to give 3.9 g of the desired product as a white solid, m.p. 106°-109° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05231182
Source datasetuspto-grants-1993_07
ORD IDord-d0a4419670384bb5b931167546fc5442
Source noteuspto-grants-1993_07