関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Isonicotinic Acid | HCID 5922 | — |
| 反応物 | P-Anisidine | HCID 7732 | — |
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | Propylphosphonic anhydride | HCID 111923 | — |
| 溶媒 | Ethyl Acetate | HCID 8857 | — |
| 生成物 | N-(4-methoxyphenyl)pyridine-4-carboxamide | HCID 532207 | 88% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07429665B2 |
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| 出典データセット | uspto-grants-2008_09 |
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| ORD ID | ord-1d9c6cc5ff654151b13c4dd5eca8c035 |
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| 出典メモ | uspto-grants-2008_09 |
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