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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1811302생성일: 2026년 10월 27일

Piperidine → acetic acid 1-(5-fluoro-2-oxo-2,3-dihydro-1H-indol-6-ylcarbamoyl)-1-methyl-ethyl ester

https://huagongshe.com/reaction/1811302

반응식

참여 물질

역할이름HCID투입량
반응물PiperidineHCID 8082—
반응물2-Acetoxyisobutyroyl chlorideHCID 123496—
반응물6-Amino-5-fluoroindolin-2-oneHCID 10103504—
용매TetrahydrofuranHCID 8028—
생성물acetic acid 1-(5-fluoro-2-oxo-2,3-dihydro-1H-indol-6-ylcarbamoyl)-1-methyl-ethyl esterHCID 5925010099.5%

반응 조건

온도-40 °C

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08362251B2
출처 데이터셋uspto-grants-2013_01
ORD IDord-f7d850e461434bf9a4d0017ec95cd023
출처 메모uspto-grants-2013_01