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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 915052Erstellt: 25. Oktober 2026

Tert-butyl (2-{[1-(1-isopropyl-6-oxo-1,6-dihydro-3-pyridazinyl)-2-oxo-2-phenylethyl]amino}-2-oxoethyl)carbamate → HCID 178456633, Verbindung

https://huagongshe.com/reaction/915052

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTert-butyl (2-{[1-(1-isopropyl-6-oxo-1,6-dihydro-3-pyridazinyl)-2-oxo-2-phenylethyl]amino}-2-oxoethyl)carbamateHCID 86600908—
LösungsmittelHydrochloric AcidHCID 313—
LösungsmittelMethanolHCID 887—
LösungsmittelPyridineHCID 1049—
ProduktHCID 178456633HCID 17845663329,1%

Reaktionsbedingungen

Temperatur82.5 °C

Reaktionsschritte

A solution of tert-butyl (2-{[1-(1-isopropyl-6-oxo-1,6-dihydro-3-pyridazinyl)-2-oxo-2-phenylethyl]amino}-2-oxoethyl)carbamate (310 mg) in 10% hydrogen chloride in MeOH (3 ml) was stirred at 20-25° C. for 18 hours and the mixture was concentrated under reduced pressure to give a residue. The residue was dissolved in pyridine (1.5 ml) and heated at 80-85° C. for 10 hours. After evaporation of pyridine, the mixture was dissolved in CHCl3, washed with 1N HCl, sat. aq. NaHCO3 and brine, dried over MgSO4 and concentrated under reduced pressure to give syrup. The syrup was purified by column chromatography on silica gel eluting with a mixture of n-hexane and EtOAc (40:60 v/v) to give 6-(6-hydroxy-3-phenyl-2-pyrazinyl)-2-isopropyl-3(2H)-pyridazinone as a solid (65 mg).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07265120B2
Quelldatensatzuspto-grants-2007_09
ORD IDord-6dcc2126a1a142d8914a67b900e8af3f
Quellennotizuspto-grants-2007_09