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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 5732Erstellt: 24. Oktober 2026

Hydrochloric Acid → N-{1-(p-methoxybenzyl)-2-(4-oxopiperidino)ethyl}-N-methyl-5-isoquinolinesulfonamide

https://huagongshe.com/de/reaction/5732

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktMethyl iodideHCID 6328—
EduktPotassium CarbonateHCID 11430—
Edukttetrahydrofuran N,N-dimethylformamideHCID 21974620—
EduktN-{2-(4,4-ethylenedioxypiperidino)-1-[p-(5-isoquinolinesulfonyloxy)benzyl]ethyl}-N-methyl-5-isoquinolinesulfonamideHCID 53669357—
ProduktN-{1-(p-methoxybenzyl)-2-(4-oxopiperidino)ethyl}-N-methyl-5-isoquinolinesulfonamideHCID 19796293—

Reaktionsschritte

The amorphous compound obtained in Example 94 was subjected to alkaline hydrolysis, methylation with methyl iodide and potassium carbonate in dimethylformamide/tetrahydrofuran (1:1), and reflux with 3N hydrochloric acid, to obtain N-{1-(p-methoxybenzyl)-2-(4-oxopiperidino)ethyl}-N-methyl-5-isoquinolinesulfonamide in a colorless amorphous form.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05245034
Quelldatensatzuspto-grants-1993_09
ORD IDord-941e293f0a7c46e8b8635a04d61fecdf
Quellennotizuspto-grants-1993_09