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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1895286Generated: November 1, 2026

Phenylhydrazine → HCID 58072343, compound

https://huagongshe.com/reaction/1895286

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylhydrazineHCID 7516—
ReactantHCID 66711108HCID 66711108—
SolventMethanolHCID 887—
ProductHCID 58072343HCID 580723436%

Reaction Steps

To a solution of 4-{3-[3-(dimethylamino)prop-2-enoyl]-4-oxopyridazin-1(4H)-yl}benzamide (crude 682 mg, 2.19 mmol) in 20 mL of methanol was added phenylhydrazine (946 mg, 8.76 mmol). The mixture was refluxed for 4 h and concentrated. The residue was dissolved in dichloromethane (20 mL), washed with 1N HCl aqueous solution and brine, dried over Na2SO4, and concentrated under reduced pressure. The residue was purified by prep-HPLC to give 4-[4-oxo-3-(1-phenyl-1H-pyrazol-5-yl)pyridazin-1(4H)-yl]benzamide (50 mg, 6% for two steps) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08513251B2
Source datasetuspto-grants-2013_08
ORD IDord-541278c739ab4740a35262ac499cd7e4
Source noteuspto-grants-2013_08