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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 483574Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/483574

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPyridineHCID 1049—
Edukt4-(2-methyl-1H-imidazol-1-yl)anilineHCID 3157478—
Eduktp-TetradecyloxyphenylacetylchlorideHCID 10021844—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktN-[4-(2-methyl-1H-imidazol-1-yl)phenyl]-4-(tetradecyloxy)benzeneacetamideHCID 1503016258,3%

Reaktionsschritte

To a solution of 5.0 g of p-tetradecyloxy phenylacetyl 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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05225425
Quelldatensatzuspto-grants-1993_07
ORD IDord-ea21e8825c33429fa7ccfbd8f74d2288
Quellennotizuspto-grants-1993_07