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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 983105생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/983105

반응식

참여 물질

역할이름HCID투입량
반응물3,5-dimethyl-4-(4-methylpiperazine-1-carbonyl)-1H-pyrrole-2-carbaldehydeHCID 12111582—
반응물4-(3-Methoxy-phenyl)-1,3-dihydro indol-2-oneHCID 22561809—
촉매PiperidineHCID 8082—
용매EthanolHCID 702—
생성물3-[3,5-dimethyl 4-(4-methyl-piperazine-1-carbonyl)-1H-pyrrol-2-ylmethylene]-4-(3-methoxy-phenyl)-1,3-dihydro-indol-2-oneHCID 2494265453%

반응 단계

To a solution of 4-(3-methoxy-phenyl)-1,3-dihydro indol-2-one (59.8 mg, 0.25 mmol) and 3,5-dimethyl-4-(4-methyl-piperazine-1-carbonyl)-1H-pyrrole-2-carbaldehyde (64.8 mg, 0.25 mmol) in ethanol (2 mL) was added piperidine (3 drops). The reaction mixture was stirred at room temperature for three days. The reaction solution was evaporated, and purified on a silica gel column eluting with MeOH—CH2Cl2 5:95 to provide 3-[3,5-dimethyl 4-(4-methyl-piperazine-1-carbonyl)-1H-pyrrol-2-ylmethylene]-4-(3-methoxy-phenyl)-1,3-dihydro-indol-2-one as a yellow solid (62 mg, 53%)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06861418B2
출처 데이터셋uspto-grants-2005_03
ORD IDord-e4490566b70c4db382dd8d38eb7cf348
출처 메모uspto-grants-2005_03