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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1016373생성일: 2026년 10월 27일

6,11-dihydro-11-[1-[2-[4-(2-quinolinylmethoxy)phenyl]ethyl]-4-piperidinylidene]-5H-imidazo[2,1-b][3]benzazepine-3-methanol → 6,11-dihydro-11-[1-[2-[4-(2-quinolinylmethoxy)phenyl]ethyl]-4-piperidinylidene]-5H-imidazo[2,1-b][3]benzazepine-3-carboxaldehyde

https://huagongshe.com/reaction/1016373

반응식

참여 물질

역할이름HCID투입량
반응물6,11-dihydro-11-[1-[2-[4-(2-quinolinylmethoxy)phenyl]ethyl]-4-piperidinylidene]-5H-imidazo[2,1-b][3]benzazepine-3-methanolHCID 9829168—
촉매HCID 178418406HCID 178418406—
용매DichloromethaneHCID 6344—
생성물6,11-dihydro-11-[1-[2-[4-(2-quinolinylmethoxy)phenyl]ethyl]-4-piperidinylidene]-5H-imidazo[2,1-b][3]benzazepine-3-carboxaldehydeHCID 991566483%

반응 단계

Compound 2 (206 g) was dissolved in DCM (11 l) under continuous stirring. Manganese dioxide (450 g) was added in 100-g portions and the resulting reaction mixture was stirred for 1 hour. The mixture was filtered over dicalite and the filtrate was evaporated. The residue was stirred in ACN, filtered off and dried, yielding 170 g (83%) of 6,11-dihydro-11-[1-[2-[4-(2-quinolinylmethoxy)phenyl]ethyl]-4-piperidinylidene]-5H-imidazo[2,1-b][3]benzazepine-3-carboxaldehyde (compound 4, mp. 193.5° C.).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06476018B1
출처 데이터셋uspto-grants-2002_11
ORD IDord-3bc40fb528fc4b6485893ccabbd84699
출처 메모uspto-grants-2002_11