Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 905843생성일: 2026년 10월 26일
Piperidine → acetic acid 1-(5-fluoro-2-oxo-2,3-dihydro-1H-indol-6-ylcarbamoyl)-1-methyl-ethyl ester
https://huagongshe.com/reaction/905843
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Piperidine | HCID 8082 | — |
| 반응물 | 2-Acetoxyisobutyroyl chloride | HCID 123496 | — |
| 반응물 | 6-Amino-5-fluoroindolin-2-one | HCID 10103504 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | acetic acid 1-(5-fluoro-2-oxo-2,3-dihydro-1H-indol-6-ylcarbamoyl)-1-methyl-ethyl ester | HCID 59250100 | 99.5% |
반응 단계
A stirred solution of 5-fluoro-6-amino-1,3-dihydro-indol-2-one (410 mg, 2.46 mmol) in 10 ml of tetrahydrofuran was added with piperidine (0.3 ml). The mixture was cooled to −40° C. in an acetone-dry ice bath and added with acetic acid 1-chlorocarbonyl-1-methyl-ethyl ester (405 mg, 2.46 mmol) in 10 ml of tetrahydrofuran dropwise. Upon the completion of the addition, the resulting mixture was stirred at the room temperature overnight until the precipitate was formed. The solid was filtered, washed with water and recrystallized from methanol to give acetic acid 1-(5-fluoro-2-oxo-2,3-dihydro-1H-indol-6-ylcarbamoyl)-1-methyl-ethyl ester (720 mg, 99.5%) as a white solid.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08012966B2 |
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| 출처 데이터셋 | uspto-grants-2011_09 |
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| ORD ID | ord-032d03c0b0ae423ba66aa3e635e8c7b4 |
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| 출처 메모 | uspto-grants-2011_09 |
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