Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2236881Erstellt: 26. Oktober 2026

Hydrochloric Acid → 4-aminomethyl-1-phenyl-1H-pyridin-2-one

https://huagongshe.com/reaction/2236881

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktTert-butyl (2-oxo-1-phenyl-1,2-dihydropyridin-4-ylmethyl)-carbamateHCID 42625677—
Lösungsmittel1,4-DioxaneHCID 31275—
Produkt4-aminomethyl-1-phenyl-1H-pyridin-2-oneHCID 42625679—

Reaktionsschritte

Tert-butyl (2-oxo-1-phenyl-1,2-dihydropyridin-4-ylmethyl)-carbamate (83 mg, 0.28 mmol) is treated with 4N hydrogen chloride in dioxane in order to remove the Boc protecting group. The hydrochloride salt of 4-aminomethyl-1-phenyl-1H-pyridin-2-one, obtained after concentration of the reaction mixture, is dissolved in N,N-dimethylformamide (5 mL) and is coupled to (4E)-6-iodo-4-(methoxymethylene)isoquinoline-1,3(2H,4H)-dione (92 mg, 0.28 mmol) in the presence of triethylamine (200 μL). After one hour, the reaction mixture is concentrated under reduced pressure and purified by flash silica gel chromatography (methanol/chloroform) to provide (4Z)-6-iodo-4-({[(2-oxo-1-phenyl-1,2dihydropyridin-4-yl)methyl]amino}methylene)isoquinoline-1,3(2H,4H)-dione as a pale yellow solid (8.8 mg, 6.3%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07713994B2
Quelldatensatzuspto-grants-2010_05
ORD IDord-82f64a456fe64485ab95f97483ea8b69
Quellennotizuspto-grants-2010_05