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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 324303Erstellt: 24. Oktober 2026

Acetic Acid → Laniquidar

https://huagongshe.com/de/reaction/324303

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 (5.5l) 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.).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06218381B1
Quelldatensatzuspto-grants-2001_04
ORD IDord-69d413a1fee24b8a8c8d8ac9b3c8f403
Quellennotizuspto-grants-2001_04