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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1624723Generated: November 1, 2026

Phenylhydrazine → HCID 59436234, compound

https://huagongshe.com/reaction/1624723

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylhydrazineHCID 7516—
ReactantHCID 66710861HCID 66710861—
SolventMethanolHCID 887—
ProductHCID 59436234HCID 594362345%

Reaction Steps

To a solution of 3-[3-(dimethylamino)prop-2-enoyl]-1-(2-methoxyphenyl)pyridazin-4(1H)-one (crude 639 mg, 2.14 mmol) in 20 mL of methanol was added phenylhydrazine (347 mg, 3.21 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-methoxyphenyl)-3-(1-phenyl-1H-pyrazol-5-yl)pyridazin-4(1H)-one (35 mg, 5% for two steps) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08778944B2
Source datasetuspto-grants-2014_07
ORD IDord-3f63dc009a084dd4b41e612641da3613
Source noteuspto-grants-2014_07