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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1016375Erstellt: 24. Oktober 2026

Acetic Acid → Laniquidar

https://huagongshe.com/de/reaction/1016375

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktSodium CyanateHCID 517096—
Edukt6,11-dihydro-11-[1-[2-[4-(2-quinolinylmethoxy)phenyl]ethyl]-4-piperidinylidene]-5H-imidazo[2,1-b][3]benzazepine-3-carboxaldehydeHCID 9915664—
KatalysatorHCID 178418406HCID 178418406—
LösungsmittelMethanolHCID 887—
ProduktLaniquidarHCID 645080687,9%

Reaktionsschritte

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.).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06476018B1
Quelldatensatzuspto-grants-2002_11
ORD IDord-1a2647c23b4245aaa0854e2afacd6b86
Quellennotizuspto-grants-2002_11