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HRID 640990作成日:2026年10月25日

Tetrahydrofuran → 5-chloro-1-methyl-N-[3-[3-[[4-(4-methylpiperazin-1-yl)anilino]methylidene]-2-oxo-1H-indole-6-carbonyl]phenyl]pyrazole-4-carboxamide

https://huagongshe.com/reaction/640990

反応式

関与物質

役割名称HCID仕込み量
反応物TetrahydrofuranHCID 8028—
反応物4-(4-Methylpiperazin-1-yl)anilineHCID 737253—
反応物HCID 178481853HCID 178481853—
溶媒Ethyl AcetateHCID 8857—
生成物5-chloro-1-methyl-N-[3-[3-[[4-(4-methylpiperazin-1-yl)anilino]methylidene]-2-oxo-1H-indole-6-carbonyl]phenyl]pyrazole-4-carboxamideHCID 17848071771%

反応条件

温度65 °C

反応手順

A small screw cap test tube was charged with 5-Chloro-1-methyl-1H-pyrazole-4-carboxylic acid [3-(3-hydroxymethylene-2-oxo-2,3-dihydro-1H-indole-6-carbonyl)-phenyl]-amide (prepared below, 100 mg, 0.237 mmol) and THF (2.5 mL). To the resulting solution was added 4-(4-methyl-piperazin-1-yl)-phenylamine (59.2 mg, 0.309 mmol), and the mixture was stirred for 24 h at 65° C. Subsequently, the reaction mixture was cooled to room temperature and diluted with EtOAc (5 mL) and Hexanes (40 mL). The precipitate that formed was then filtered and washed with acetone (5 mL) to afford the title compound in 71% yield (0.100 g, 0.168 mmol).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07692005B2
出典データセットuspto-grants-2010_04
ORD IDord-201069fda86b42358b0f52a58be54e5c
出典メモuspto-grants-2010_04