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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1624721Generated: October 29, 2026

Phenylhydrazine → HCID 59370088, compound

https://huagongshe.com/reaction/1624721

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylhydrazineHCID 7516—
ReactantHCID 2745040HCID 2745040—
SolventMethanolHCID 887—
ProductHCID 59370088HCID 5937008812%

Reaction Steps

To a solution of 3-[3-(dimethylamino)prop-2-enoyl]-1-[4-(trifluoromethyl)phenyl]pyridazin-4(1H)-one (crude 718 mg, 2.13 mmol) in 20 mL of methanol was added phenylhydrazine (345 mg, 3.20 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-[4-(trifluoromethyl)phenyl]pyridazin-4(1H)-one (100 mg, 12% for two steps) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08778944B2
Source datasetuspto-grants-2014_07
ORD IDord-b56011d0ae3f4c508c8329008cae342a
Source noteuspto-grants-2014_07