Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 915052Generated: October 25, 2026

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

https://huagongshe.com/reaction/915052

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl (2-{[1-(1-isopropyl-6-oxo-1,6-dihydro-3-pyridazinyl)-2-oxo-2-phenylethyl]amino}-2-oxoethyl)carbamateHCID 86600908—
SolventHydrochloric AcidHCID 313—
SolventMethanolHCID 887—
SolventPyridineHCID 1049—
ProductHCID 178456633HCID 17845663329.1%

Reaction Conditions

Temperature82.5 °C

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07265120B2
Source datasetuspto-grants-2007_09
ORD IDord-6dcc2126a1a142d8914a67b900e8af3f
Source noteuspto-grants-2007_09