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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 33943생성일: 2026년 10월 23일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물Isonicotinic AcidHCID 5922—
반응물P-AnisidineHCID 7732—
반응물TriethylamineHCID 8471—
반응물Propylphosphonic anhydrideHCID 111923—
용매Ethyl AcetateHCID 8857—
생성물N-(4-methoxyphenyl)pyridine-4-carboxamideHCID 53220788%

반응 조건

온도23 °C

반응 단계

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)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07429665B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-1d9c6cc5ff654151b13c4dd5eca8c035
출처 메모uspto-grants-2008_09