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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1016375생성일: 2026년 10월 25일

Acetic Acid → Laniquidar

https://huagongshe.com/reaction/1016375

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물Sodium CyanateHCID 517096—
반응물6,11-dihydro-11-[1-[2-[4-(2-quinolinylmethoxy)phenyl]ethyl]-4-piperidinylidene]-5H-imidazo[2,1-b][3]benzazepine-3-carboxaldehydeHCID 9915664—
촉매HCID 178418406HCID 178418406—
용매MethanolHCID 887—
생성물LaniquidarHCID 645080687.9%

반응 단계

A mixture of compound 4 (164 g), sodium cyanate (80 g) and manganese dioxide (500 g) in methanol (5.5 l) was stirred at room temperature. Ethanoic acid (122 g) was added dropwise and the resulting reaction mixture was stirred and refluxed overnight. The reaction mixture was filtered over dicalite, and the filter residue was rinsed with CH3OH/CH2Cl2. The filtrate was evaporated. The residue was partitioned between DCM and aqueous K2CO3 solution. The organic layer was separated, dried (MgSO4), filtered and the solvent was evaporated. The residue was crystallized from ACN. The precipitate was filtered off and dried, yielding 152 g (87%) of methyl 6,11-dihydro-11-[1-[2-[4-(2-quinolinylmethoxy)phenyl]ethyl]-4-piperidinylidene]-5H-imidazo[2,1-b][3]-benzazepine-3-carboxylate (compound 6, mp. 179.3° C.).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06476018B1
출처 데이터셋uspto-grants-2002_11
ORD IDord-1a2647c23b4245aaa0854e2afacd6b86
출처 메모uspto-grants-2002_11