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HRID 1016375作成日:2026年10月26日

Acetic Acid → Laniquidar

https://huagongshe.com/reaction/1016375

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物Sodium CyanateHCID 517096—
反応物6,11-dihydro-11-[1-[2-[4-(2-quinolinylmethoxy)phenyl]ethyl]-4-piperidinylidene]-5H-imidazo[2,1-b][3]benzazepine-3-carboxaldehydeHCID 9915664—
触媒HCID 178418406HCID 178418406—
溶媒MethanolHCID 887—
生成物LaniquidarHCID 645080687.9%

反応手順

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.).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06476018B1
出典データセットuspto-grants-2002_11
ORD IDord-1a2647c23b4245aaa0854e2afacd6b86
出典メモuspto-grants-2002_11