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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 983142생성일: 2026년 10월 24일

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-trifluoromethyl-phenyl)-1,3-dihydro-indol-2-one

https://huagongshe.com/ko/reaction/983142

반응식

참여 물질

역할이름HCID투입량
반응물3,5-dimethyl-4-(4-methylpiperazine-1-carbonyl)-1H-pyrrole-2-carbaldehydeHCID 12111582—
반응물4-(3-Trifluoromethyl-phenyl)-1,3-dihydro-indol-2-oneHCID 22561905—
촉매PiperidineHCID 8082—
용매EthanolHCID 702—
생성물3-[3,5-dimethyl-4-(4-methyl-piperazine-1-carbonyl)-1H-pyrrol-2-ylmethylene]-4-(3-trifluoromethyl-phenyl)-1,3-dihydro-indol-2-oneHCID 2494266076%

반응 단계

To a solution of 4-(3-trifluoromethyl-phenyl)-1,3-dihydro-indol-2-one (69.3 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. The solvent was evaporated and the solid was washed by ether for three times to provide pure product 3-[3,5-dimethyl-4-(4-methyl-piperazine-1-carbonyl)-1H-pyrrol-2-ylmethylene]-4-(3-trifluoromethyl-phenyl)-1,3-dihydro-indol-2-one (96.5 mg, 76%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06861418B2
출처 데이터셋uspto-grants-2005_03
ORD IDord-f8e11c8bf4064fa3b6827fc6cda19313
출처 메모uspto-grants-2005_03