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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 469200생성일: 2026년 10월 26일

Diisopropylethylamine → 3-(2-Ethoxypyridin-3-yl)-3-[4-(4-methylpiperazin-1-ylmethyl)phenylamino]-2-oxo-2,3-dihydro-1H-indole-5-carbonitrile

https://huagongshe.com/reaction/469200

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물Sodium BicarbonateHCID 516892—
반응물4-((4-Methylpiperazin-1-yl)methyl)anilineHCID 3153996—
반응물3-Chloro-3-(2-ethoxypyridin-3-yl)-2-oxoindoline-5-carbonitrileHCID 67048504—
용매DichloromethaneHCID 6344—
생성물3-(2-Ethoxypyridin-3-yl)-3-[4-(4-methylpiperazin-1-ylmethyl)phenylamino]-2-oxo-2,3-dihydro-1H-indole-5-carbonitrileHCID 67198064103.1%

반응 단계

4-(4-Methyl-piperazin-1-ylmethyl)phenylamine (425 mg, 2.07 mmol) was added to a solution of 3-chloro-3-(2-ethoxypyridin-3-yl)-2-oxo-2,3-dihydro-1H-indole-5-carbonitrile (500 mg, 1.59 mmol) in dichloromethane (50 ml) and DIPEA (0.27 ml, 159 mmol) at 0° C. The reaction mixture was stirred at room temperature for 2 h and then an aqueous NaHCO3 solution was added. The aqueous reaction mixture was extracted with dichloromethane. The combined organic phase was dried over magnesium sulfate, filtered and concentrated at reduced pressure. Purification by chromatography (silica gel, 0-20% methanol in dichloromethane) afforded 791 mg of the title compound (99% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08629148B2
출처 데이터셋uspto-grants-2014_01
ORD IDord-2bd343301a104a76b3c1f9c82d82b970
출처 메모uspto-grants-2014_01