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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1839814생성일: 2026년 10월 25일

4-(3-Piperidin-1-yl-propionyl)-1,4,5,6,7,8-hexahydro-pyrrolo[3,2-b]azepine-2-carbaldehyde → 4-(2,6-Difluoro-phenyl)-3-[1-[4-(3-piperidin-1-yl-propionyl)-1,4,5,6,7,8-hexahydro-pyrrolo[3,2-b]azepin-2-yl]-meth-(z)-ylidene]-1,3-dihydro-indol-2-one

https://huagongshe.com/reaction/1839814

반응식

참여 물질

역할이름HCID투입량
반응물4-(3-Piperidin-1-yl-propionyl)-1,4,5,6,7,8-hexahydro-pyrrolo[3,2-b]azepine-2-carbaldehydeHCID 22561698—
반응물4-(2,6-Difluoro-phenyl)-1,3-dihydro-indol-2-oneHCID 22561746—
촉매PiperidineHCID 8082—
용매EthanolHCID 702—
생성물4-(2,6-Difluoro-phenyl)-3-[1-[4-(3-piperidin-1-yl-propionyl)-1,4,5,6,7,8-hexahydro-pyrrolo[3,2-b]azepin-2-yl]-meth-(z)-ylidene]-1,3-dihydro-indol-2-oneHCID 6006128160.3%

반응 단계

4-(3-Piperidin-1-yl-propionyl)-1,4,5,6,7,8-hexahydro-pyrrolo[3,2-b]azepine-2-carbaldehyde (80 mg, 0.26 mmol) was condensed with 4-(2,6-difluoro-phenyl)-1,3-dihydro-indol-2-one (61 mg, 0.25 mmol) and piperidine (1 drop) in ethanol (3 mL) at rt for over the weekend. The precipitate was filtered, washed with ethanol and dried to give 80 mg of the titled compound as a yellow solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06677368B2
출처 데이터셋uspto-grants-2004_01
ORD IDord-2667cd709f224fc8b4fa69b148d196c3
출처 메모uspto-grants-2004_01