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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1402062Generated: October 26, 2026

Acetonitrile → 5-chloro-2,4-difluoro-N-pyridazin-3-ylbenzenesulfonamide

https://huagongshe.com/reaction/1402062

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantDabcoHCID 9237—
ReactantAminopyridazineHCID 230373—
Reactant5-Chloro-2,4-difluorobenzenesulphonyl chlorideHCID 2773527—
Product5-chloro-2,4-difluoro-N-pyridazin-3-ylbenzenesulfonamideHCID 5943655624.9%

Reaction Steps

Pyridazin-3-amine (1.00 g, 10.5 mmol) and triethylenediamine (1.18 g, 10.5 mmol) was added concurrently to a solution of 5-chloro-2,4-difluorobenzenesulfonyl chloride (2.60 g, 10.5 mmol) in acetonitrile (50 mL, 1000 mmol). The reaction mixture was stirred for 18 h then concentrated. The residue was dissolved in ethyl acetate (30 mL), washed with water, brine, dried over sodium sulfate and concentrated. The residue was purified on automated silica gel chromatography (chloroform to 50% of 10% methanol in chloroform) to give 800 mg of the desired product as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08907101B2
Source datasetuspto-grants-2014_12
ORD IDord-399920cb9fc04d8385b6711978db577e
Source noteuspto-grants-2014_12