Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 13359생성일: 2026년 10월 24일
Acetic Anhydride → N-(5-(6-(1-acetyl-pyrrolidin-2-yl)-2-pyridin-2-yl-1H-benzimidazol-5-yloxy)-pyridin-2-yl)-acetamide
https://huagongshe.com/ko/reaction/13359
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Acetic Anhydride | HCID 7918 | — |
| 반응물 | 1-(2-(6-(6-amino-pyridin-3-yloxy)-2-pyridin-2-yl-3H-benzimidazol-5-yl)-pyrrolidin-1-yl)-ethanone | HCID 23145367 | — |
| 용매 | Pyridine | HCID 1049 | — |
| 생성물 | N-(5-(6-(1-acetyl-pyrrolidin-2-yl)-2-pyridin-2-yl-1H-benzimidazol-5-yloxy)-pyridin-2-yl)-acetamide | HCID 11190297 | — |
반응 단계
0.005 ml of acetic anhydride was added to a pyridine (1 ml) solution of 13.7 mg of 1-(2-(6-(6-amino-pyridin-3-yloxy)-2-pyridin-2-yl-3H-benzimidazol-5-yl)-pyrrolidin-1-yl)-ethanone, and the reaction liquid was stirred at room temperature for 3 hours. The reaction liquid was evaporated away under reduced pressure, the resulting residue was dissolved in 1 ml of trifluoroacetic acid, and the reaction liquid was stirred at room temperature for 3 hours. The reaction liquid was distilled under reduced pressure, and the resulting residue was purified through reversed-phase middle-pressure liquid chromatography [ODS-AS-360-CC (by YMC), mobile phase: water-acetonitrile-0.1% trifluoroacetic acid] and through silica gel column chromatography (developing solvent: chloroform/methanol=9/1) to obtain the entitled compound as an oily substance.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07728025B2 |
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| 출처 데이터셋 | uspto-grants-2010_06 |
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| ORD ID | ord-418d477eaeb94b2faa09eaad87323df2 |
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| 출처 메모 | uspto-grants-2010_06 |
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