関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Toluene | HCID 1140 | — |
| 反応物 | Phosgene | HCID 6371 | — |
| 反応物 | Methanesulfonic Acid | HCID 6395 | — |
| 反応物 | Quinoline | HCID 7047 | — |
| 反応物 | 2-amino-N-(4-methoxyphenyl)benzamide | HCID 478820 | — |
| 反応物 | 1-(Pyridin-4-yl)piperidin-4-ol | HCID 23447619 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | N-(4-Methoxyphenyl)-2-[1-(4-pyridinyl)piperidin-4-yloxycarbonyl]aminobenzamide | HCID 18174418 | 46% |
反応手順
To a mixture of 1-(4-pyridyl)-4-hydroxypiperidine (536 mg, 3.01 mmol) and methylene chloride (45 mL) was added methanesulfonic acid (0.2 ml, 3.1 mmol). After stirring for 15 seconds, quinoline (0.45 mL, 3.8 mmol) was added, immediately followed by 1.93 M phosgene in toluene (2 mL, 3.9 mmol). After 5 minutes, the reaction was placed in a 35° C. oil bath for 45 minutes. The reaction was cooled to room temperature and N-(4-methoxyphenyl)-2-aminobenzamide (728 mg, 3.0 mmol) and quinoline(0.45 mL, 3.8 mmol) were added. After stirring overnight, the reaction was diluted with CH2Cl2(150 mL) and washed with sat'd sodium carbonate (2×25 mL). The organic layer was concentrated and the crude residue was chromatographed to give 617 mg (46%) of the title compound as a white solid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06605626B2 |
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| 出典データセット | uspto-grants-2003_08 |
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| ORD ID | ord-2df88400879e4876b1fd1e7676a166ee |
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| 出典メモ | uspto-grants-2003_08 |
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