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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 133106Erstellt: 25. Oktober 2026

4-Pyridinecarboxaldehyde → 2-(4-tert-butyl-phenyl)-8-[(pyridin-4-ylmethyl)-amino]-2H-phthalazin-1-one

https://huagongshe.com/reaction/133106

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-PyridinecarboxaldehydeHCID 13389—
EduktP-ToluenesulfonylhydrazideHCID 15303—
EduktSodium triacetoxyborohydrideHCID 5049666—
Edukt8-amino-2-(4-tert-butyl-phenyl)-2H-phthalazin-1-oneHCID 69160627—
LösungsmittelDichloromethaneHCID 6344—
Produkt2-(4-tert-butyl-phenyl)-8-[(pyridin-4-ylmethyl)-amino]-2H-phthalazin-1-oneHCID 11406487—

Reaktionsschritte

To a solution of the amine (Step E, 45 mg, 0.15 mmol) and CH2Cl2 (10 mL) was added 4-pyridinecarboxaldehyde (0.04 mL, 0.39 mmol) and NaBH(OAc)3 (95 mg, 0.45 mmol). The reaction was stirred at RT for 7 h then quenched with H2O and extracted with CH2Cl2. The organic layer was washed with H2O and brine, dried (MgSO4) and concentrated in vacuo to give the crude product as an orange oil. The crude product was dissolved in 10 mL CH2Cl2 and stirred with PS-TsNHNH2 resin to remove un-reacted aldehyde. After 1 h, the mixture was filtered through Celite® and concentrated in vacuo. The residue was purified by silica flash chromatography (20-75% EtOAc:hexane) to give the desired product as a light-yellow crystalline solid. MS m/e 385 (M+H)+. Calc'd for C24H24N4O-384.47.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07390820B2
Quelldatensatzuspto-grants-2008_06
ORD IDord-f5fd2b5e61724521a6e8851896d5c524
Quellennotizuspto-grants-2008_06