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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 467508Generated: October 30, 2026

3-[3-(3,5-difluorophenyl)-6-oxo-6H-pyridazin-1-ylmethyl]-N-(2-oxoethyl)benzamide → 6-(3,5-difluorophenyl)-2-(3-oxazol-2-ylbenzyl)-2H-pyridazin-3-one

https://huagongshe.com/reaction/467508

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-[3-(3,5-difluorophenyl)-6-oxo-6H-pyridazin-1-ylmethyl]-N-(2-oxoethyl)benzamideHCID 58497249—
Reactant(Methoxycarbonylsulfamoyl)triethylammonium betaineHCID 86658973—
SolventTetrahydrofuranHCID 8028—
Product6-(3,5-difluorophenyl)-2-(3-oxazol-2-ylbenzyl)-2H-pyridazin-3-oneHCID 58497253—

Reaction Steps

A solution of 1.01 g (2.64 mmol) of 3-[3-(3,5-difluorophenyl)-6-oxo-6H-pyridazin-1-ylmethyl]-N-(2-oxoethyl)benzamide and 1.26 g (5.27 mmol) of (methoxycarbonylsulfamoyl)triethylammonium betaine (Burgess reagent) in 5.3 ml of THF is stirred at a temperature of 150° C. in a sealed vessel for 5 minutes. The reaction mixture is partitioned between saturated sodium hydrogencarbonate solution and dichloromethane. The organic phase is dried over sodium sulfate and evaporated. The residue is chromatographed on a silica-gel column with dichloromethane/methanol as eluent, giving 6-(3,5-difluorophenyl)-2-(3-oxazol-2-ylbenzyl)-2H-pyridazin-3-one as colourless crystals; ESI 366.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08623870B2
Source datasetuspto-grants-2014_01
ORD IDord-c633d1c528954f0e942484e7e623ae16
Source noteuspto-grants-2014_01