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HRID 1839687作成日:2026年10月27日

3,5-dimethyl-4-(4-methylpiperazine-1-carbonyl)-1H-pyrrole-2-carbaldehyde → 3-[3,5-dimethyl-4-(4-methyl-piperazine-1-carbonyl)-1H-pyrrol-2-ylmethylene]-4-(3-fluoro-phenyl)1,3-dihydro-indol-2-one

https://huagongshe.com/reaction/1839687

反応式

関与物質

役割名称HCID仕込み量
反応物3,5-dimethyl-4-(4-methylpiperazine-1-carbonyl)-1H-pyrrole-2-carbaldehydeHCID 12111582—
反応物4-(3-Fluoro-phenyl)-1,3-dihydro-indol-2-oneHCID 22561756—
触媒PiperidineHCID 8082—
溶媒EthanolHCID 702—
生成物3-[3,5-dimethyl-4-(4-methyl-piperazine-1-carbonyl)-1H-pyrrol-2-ylmethylene]-4-(3-fluoro-phenyl)1,3-dihydro-indol-2-oneHCID 2494264757%

反応手順

To a solution of 4-(3-fluoro-phenyl)-1,3-dihydro-indol-2-one (56.8 mg, 0.25 mmol) and 3,5-dimethyl-4-(4-methyl-piperazine-1-carbonyl)-1H-pyrrole-2-carbaldehyde (64.8 mg, 0.26 mmol) in ethanol (2 mL) was added piperidine (3 drops). The reaction mixture was stirred at room temperature for three days. A yellow solid product was precipitated out, filtered, washed by ethanol for three times, and dried under high vacuum to provide 3-[3,5-dimethyl-4-(4-methyl-piperazine-1-carbonyl)-1H-pyrrol-2-ylmethylene]-4-(3-fluoro-phenyl)-1,3-dihydro-indol-2-one as a yellow solid (65 mg, 57%)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06677368B2
出典データセットuspto-grants-2004_01
ORD IDord-d29196f894404ec381bb34dbb2f33a63
出典メモuspto-grants-2004_01