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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 324303생성일: 2026년 10월 25일

Acetic Acid → Laniquidar

https://huagongshe.com/reaction/324303

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 (5.5l) 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 번호US06218381B1
출처 데이터셋uspto-grants-2001_04
ORD IDord-69d413a1fee24b8a8c8d8ac9b3c8f403
출처 메모uspto-grants-2001_04