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HRID 33943作成日:2026年10月24日

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

https://huagongshe.com/ja/reaction/33943

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/Cl) 229.3 (M+H)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07429665B2
出典データセットuspto-grants-2008_09
ORD IDord-1d9c6cc5ff654151b13c4dd5eca8c035
出典メモuspto-grants-2008_09