戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1170382作成日:2026年10月27日

Isonicotinic Acid → N-(4-methoxyphenyl)pyridine-4-carboxamide

https://huagongshe.com/reaction/1170382

反応式

関与物質

役割名称HCID仕込み量
反応物Isonicotinic AcidHCID 5922—
反応物P-AnisidineHCID 7732—
反応物TriethylamineHCID 8471—
反応物Propylphosphonic anhydrideHCID 111923—
溶媒Ethyl AcetateHCID 8857—
生成物N-(4-methoxyphenyl)pyridine-4-carboxamideHCID 53220788%

反応条件

温度23 °C

反応手順

A solution of p-anisidine (2.46 g, 20 mmol) and triethylamine (13.9 mL, 100 mmol) in ethyl acetate (200 mL) was treated with isonicotinic acid (2.46 g, 20 mmol) followed by 1-propanephosphonic acid cyclic anhydride (50% in ethyl acetate, 15.1 mL, 24 mmol). After stirring at 23° C. for 4 h, the reaction mixture was diluted with ethyl acetate, was washed with water and with brine, and the organic layer was dried (MgSO4), was filtered, and was concentrated in vacuo. Purification by silica gel chromatography with chloroform-methanol (40:1) gave 4 g (88% yield) of the title compound; diagnostic 13C NMR signals (100 MHz, CD3OD/CDCl3) δ 164.825, 157.213, 149.758, 143.349, 130.989, 123.085, 122.068, 55.285; MS (AP/CI) 229.3 (M+H)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07825254B2
出典データセットuspto-grants-2010_11
ORD IDord-cb9ebf10226c459c87faf7af9b424872
出典メモuspto-grants-2010_11