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HRID 483574作成日:2026年10月26日

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

https://huagongshe.com/reaction/483574

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物4-(2-methyl-1H-imidazol-1-yl)anilineHCID 3157478—
反応物p-TetradecyloxyphenylacetylchlorideHCID 10021844—
溶媒TetrahydrofuranHCID 8028—
生成物N-[4-(2-methyl-1H-imidazol-1-yl)phenyl]-4-(tetradecyloxy)benzeneacetamideHCID 1503016258.3%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05225425
出典データセットuspto-grants-1993_07
ORD IDord-ea21e8825c33429fa7ccfbd8f74d2288
出典メモuspto-grants-1993_07