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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2101441Generated: October 30, 2026

Hydrochloric Acid → 6-(5-Chloro-3-methyl-benzofuran-2-sulfonyl)-2H-pyridazin 2H-pyridazin-3-one

https://huagongshe.com/reaction/2101441

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant3-Methoxy-6-(5-chloro-3-methyl-benzofuran-2-sulfonyl)-pyridazineHCID 9945813—
Solvent1,4-DioxaneHCID 31275—
Product6-(5-Chloro-3-methyl-benzofuran-2-sulfonyl)-2H-pyridazin 2H-pyridazin-3-oneHCID 69049359—

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 3-methoxy-6-(5-chloro-3-methyl-benzofuran-2-sulfonyl)-pyridazine (22.2 mmol, 7.5 g), conc. HCl (5 mL), and dioxane (50 mL) was heated at 100° C. for 2 hours. The reaction mixture was cooled and evaporated to dryness. Water (20 mL) was added to the residue. The resulting precipitate was collected and crystallized from ethanol to obtain the desired product: 6-(5-chloro-3-methyl-benzofuran-2-sulfonyl)-2H-pyridazin-2H-pyridazin-3-one (89%, 6.42 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07572910B2
Source datasetuspto-grants-2009_08
ORD IDord-e87f61e3757f4926aa3f2fbceada534f
Source noteuspto-grants-2009_08