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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1624741Generated: October 31, 2026

Phenylhydrazine → HCID 58072238, compound

https://huagongshe.com/reaction/1624741

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylhydrazineHCID 7516—
ReactantHCID 66710594HCID 66710594—
SolventMethanolHCID 887—
ProductHCID 58072238HCID 580722388.2%

Reaction Steps

To a solution of 1-(2-chlorophenyl)-3-[3-(dimethylamino)prop-2-enoyl]pyridazin-4(1H)-one (crude, 636 mg, 2.10 mmol) in 20 mL of methanol was added phenylhydrazine (907 mg, 8.40 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 1-(2-chlorophenyl)-3-(1-phenyl-1H-pyrazol-5-yl)pyridazin-4(1H)-one (60 mg, 8% for two steps) as a red gel.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08778944B2
Source datasetuspto-grants-2014_07
ORD IDord-64f119137e3c4b43b02bd12014619c7c
Source noteuspto-grants-2014_07