참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Isonicotinic Acid | HCID 5922 | — |
| 반응물 | P-Anisidine | HCID 7732 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | Propylphosphonic anhydride | HCID 111923 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | N-(4-methoxyphenyl)pyridine-4-carboxamide | HCID 532207 | 88% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07429665B2 |
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| 출처 데이터셋 | uspto-grants-2008_09 |
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| ORD ID | ord-1d9c6cc5ff654151b13c4dd5eca8c035 |
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| 출처 메모 | uspto-grants-2008_09 |
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