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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1624562Generated: November 1, 2026

Thionyl Chloride → HCID 59436266, compound

https://huagongshe.com/reaction/1624562

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 1481283HCID 1481283—
ReactantHCID 178418385HCID 178418385—
SolventDichloromethaneHCID 6344—
ProductHCID 59436266HCID 5943626658.1%

Reaction Steps

A solution of 4-Oxo-N-phenyl-1-[3-(trifluoromethyl)phenyl]-1,4-dihydropyridazine-3-carboxamide (0.153 g, 0.426 mmol), 1H-benzo[d][1,2,3]triazole (0.201 g, 1.69 mmol) and thionyl chloride (0.06 mL, 0.82 mmol) in methylene chloride (2 mL) was heated under microwave heating conditions at 80 watts of power for 10 min. After that time, the reaction was concentrated and the crude product purified by flash column chromatography (silica gel, hexanes to ethyl acetate) to give 0.114 g (58%) of 3-[1H-benzotriazol-1-yl(phenylimino)methyl]-1-[3-(trifluoromethyl)phenyl]pyridazin-4(1H)-one as a pale red solid that was used without further characterization.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08778944B2
Source datasetuspto-grants-2014_07
ORD IDord-137174e810ca4468a08696d27d5e4eae
Source noteuspto-grants-2014_07