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HRID 469200作成日:2026年10月25日

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

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylethylamineHCID 81531—
反応物Sodium BicarbonateHCID 516892—
反応物4-((4-Methylpiperazin-1-yl)methyl)anilineHCID 3153996—
反応物3-Chloro-3-(2-ethoxypyridin-3-yl)-2-oxoindoline-5-carbonitrileHCID 67048504—
溶媒DichloromethaneHCID 6344—
生成物3-(2-Ethoxypyridin-3-yl)-3-[4-(4-methylpiperazin-1-ylmethyl)phenylamino]-2-oxo-2,3-dihydro-1H-indole-5-carbonitrileHCID 67198064103.1%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08629148B2
出典データセットuspto-grants-2014_01
ORD IDord-2bd343301a104a76b3c1f9c82d82b970
出典メモuspto-grants-2014_01