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HRID 3992作成日:2026年10月23日

2-(5-Chloro-7-aminoindolin-1-yl)benzamide → 4-Chloro-1,2-dihydrobenzo[c]pyrrolo[1,2,3-ef][1,5]benzodiazepin-7-one

https://huagongshe.com/ja/reaction/3992

反応式

関与物質

役割名称HCID仕込み量
反応物2-(5-Chloro-7-aminoindolin-1-yl)benzamideHCID 13823270—
溶媒Dichloromethane methanolHCID 21226129—
生成物4-Chloro-1,2-dihydrobenzo[c]pyrrolo[1,2,3-ef][1,5]benzodiazepin-7-oneHCID 13823271—

反応手順

2-(5-chloro-7-aminoindolin-1-yl)benzamide of Example 1c (28.7 g, 0.10 mole) was dissolved in methanol/dichloromethane (DCM) solution (1:9 v/v) at 35° C. Silica gel (510 gm) was added to absorb the starting material, then the solvent was removed as much as possible under vacuum (50° C., 25 mmHg pressure for 1 hr.) The reaction mixture was then heated at 145°-155° C. and mechanically stirred for 11/2 hours. The heating was stopped when the mixture started to turn brown. The combined material was placed onto a flash chromatography column (1 kg, silica gel 60, slurry packed with DCM), eluted with DCM (16 l) and 2% CH3OH in DCM (10 l). The fractions containing the desired product were pooled and concentrated to yield a solid, 16 gm, (59%), m.p. 252°-255° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04723007
出典データセットuspto-grants-1988_02
ORD IDord-4bbfa46f3e4e40cb90638913d3ea938d
出典メモuspto-grants-1988_02