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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1407253Generated: October 30, 2026

Phenylhydrazine → HCID 59436253, compound

https://huagongshe.com/reaction/1407253

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylhydrazineHCID 7516—
ReactantHCID 66710740HCID 66710740—
SolventMethanolHCID 887—
ProductHCID 59436253HCID 5943625312%

Reaction Steps

To a solution of 3-[3-(dimethylamino)prop-2-enoyl]-1-[2-(trifluoromethyl)phenyl]pyridazin-4(1H)-one (crude 785 mg, 2.33 mmol) in 20 mL of methanol was added phenylhydrazine (377 mg, 3.50 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 3-(1-phenyl-1H-pyrazol-5-yl)-1-[2-(trifluoromethyl)phenyl]pyridazin-4(1H)-one (105 mg, 12% for two steps) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08916566B2
Source datasetuspto-grants-2014_12
ORD IDord-b6206703866f46768d304e4e74a7395d
Source noteuspto-grants-2014_12