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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 57199생성일: 2026년 10월 23일

1-(1-Methyl-4-piperidinyl)piperazine → 5-Cyano-3-(2-ethoxypyridin-3-yl)-6-fluoro-2-oxo-2,3-dihydro-1H-indol-3-yl 4-(1-methylpiperidin-4-yl)piperazine-1-carboxylate

https://huagongshe.com/ko/reaction/57199

반응식

참여 물질

역할이름HCID투입량
반응물1-(1-Methyl-4-piperidinyl)piperazineHCID 566324—
반응물Phenyl 5-cyano-3-(2-ethoxypyridin-3-yl)-6-fluoro-2-oxo-3-phenoxycarbonyloxy-2,3-dihydroindole-1-carboxylateHCID 67087492—
용매TetrahydrofuranHCID 8028—
생성물5-Cyano-3-(2-ethoxypyridin-3-yl)-6-fluoro-2-oxo-2,3-dihydro-1H-indol-3-yl 4-(1-methylpiperidin-4-yl)piperazine-1-carboxylateHCID 6708768657%

반응 단계

A mixture of 291 mg (0.53 mmol) of phenyl 5-cyano-3-(2-ethoxypyridin-3-yl)-6-fluoro-2-oxo-3-phenoxycarbonyloxy-2,3-dihydroindole-1-carboxylate, 289 mg (1.58 mmol) of 1-(1-methylpiperidin-4-yl)piperazine and 6 ml of dried tetrahydrofuran (THF) was stirred at room temperature overnight. The reaction mixture was concentrated under reduced pressure and stirred with methanol. The precipitated solid was filtered off and dried in a vacuum drying oven. 158 mg of the title compound were obtained as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09434713B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-54e74598eef943ddb12802e8cefb8ffa
출처 메모uspto-grants-2016_09