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HRID 35124作成日:2026年10月25日

2-(5-Methyl-7-nitro-1-indolinyl)benzoic acid → 4-Methyl-1,2-dihydrobenzo[c]pyrrolo[1,2,3-ef][1,5]benzodiazepin-7-one

https://huagongshe.com/reaction/35124

反応式

関与物質

役割名称HCID仕込み量
反応物2-(5-Methyl-7-nitro-1-indolinyl)benzoic acidHCID 14023680—
触媒Hydrochloric AcidHCID 313—
触媒PalladiumHCID 23938—
溶媒EthanolHCID 702—
生成物4-Methyl-1,2-dihydrobenzo[c]pyrrolo[1,2,3-ef][1,5]benzodiazepin-7-oneHCID 1382328066.6%

反応手順

To a solution of 2-(5-methyl-7-nitroindolin-1-yl)benzoic acid (9 g, 0.03 mole), conc. hydrochloric acid (several drops) and ethanol (200 ml) was added 5% palladium-charcoal (1.5 gm). The mixture was shaked under hydrogen (58 psi) for 30 hours. The solvent was removed and the residue was loaded onto a silica gel flash chromatography column (800 g, 230-400 mesh), packed and eluted with dichloromethane (4 l) and 2% methanol in dichloromethane (4 l). The fractions containing product were pooled and evaporated to yield 5 g (66%) of product. Recrystallization from chloroform gave the analytical sample, mp 222°-224° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04764616
出典データセットuspto-grants-1988_08
ORD IDord-ae5594f179fd4d2489f1d652fc044fa7
出典メモuspto-grants-1988_08