Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 395852생성일: 2026년 10월 25일
Toluene → N-(4-Methoxyphenyl)-2-[1-(4-pyridinyl)piperidin-4-yloxycarbonyl]aminobenzamide
https://huagongshe.com/reaction/395852
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Toluene | HCID 1140 | — |
| 반응물 | Phosgene | HCID 6371 | — |
| 반응물 | Methanesulfonic Acid | HCID 6395 | — |
| 반응물 | Quinoline | HCID 7047 | — |
| 반응물 | 2-amino-N-(4-methoxyphenyl)benzamide | HCID 478820 | — |
| 반응물 | 1-(Pyridin-4-yl)piperidin-4-ol | HCID 23447619 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | N-(4-Methoxyphenyl)-2-[1-(4-pyridinyl)piperidin-4-yloxycarbonyl]aminobenzamide | HCID 18174418 | 46% |
반응 단계
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.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06605626B2 |
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| 출처 데이터셋 | uspto-grants-2003_08 |
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| ORD ID | ord-2df88400879e4876b1fd1e7676a166ee |
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| 출처 메모 | uspto-grants-2003_08 |
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