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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 915056Generated: October 30, 2026

Water → 6-{5-amino-6-[(1-methyl-1H-imidazol-5-yl)ethynyl]-3-phenyl-2-pyrazinyl}-2-isopropyl-3(2H)-pyridazinone

https://huagongshe.com/reaction/915056

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
Reactant5-Ethynyl-1-methyl-1H-imidazoleHCID 3333106—
Reactant6-(5-amino-6-bromo-3-phenyl-2-pyrazinyl)-2-isopropyl-3(2H)-pyridazinoneHCID 86600915—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventTetrahydrofuranHCID 8028—
Product6-{5-amino-6-[(1-methyl-1H-imidazol-5-yl)ethynyl]-3-phenyl-2-pyrazinyl}-2-isopropyl-3(2H)-pyridazinoneHCID 1130445584.5%

Reaction Steps

In the presence of copper(I) iodide (3.7 mg) and dichlorobis(triphenylphosphine)palladium(II) (13.7 mg), triethylamine (0.0596 ml) was dropwise added to a mixture of 6-(5-amino-6-bromo-3-phenyl-2-pyrazinyl)-2-isopropyl-3(2H)-pyridazinone (150 mg) and 5-ethynyl-1-methyl-1H-imidazole (45.4 mg) in THF (1.5 ml) at 50° C. The mixture was refluxed for 2 hours. Water was added to the reaction mixture to give a solid. The solid was purified by column chromatography on silica gel eluting with a mixture of MeOH and EtOAc (2:98 v/v) to give 6-{5-amino-6-[(1-methyl-1H-imidazol-5-yl)ethynyl]-3-phenyl-2-pyrazinyl}-2-isopropyl-3(2H)-pyridazinone as a solid (135 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07265120B2
Source datasetuspto-grants-2007_09
ORD IDord-0270303b61b644139c9b2d837681ebec
Source noteuspto-grants-2007_09