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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1946443Generated: October 26, 2026

Triethylamine → 2-Chloro-6-propylimidazo[1,2-b]pyridazine-3-sulfonyl chloride

https://huagongshe.com/reaction/1946443

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantChlorosulfonic acidHCID 24638—
ReactantPhosphorus oxychlorideHCID 24813—
Reactant2-Chloro-6-propylimidazo[1,2-b]pyridazineHCID 23028095—
Solvent1,2-DichloroethaneHCID 11—
SolventWaterHCID 962—
Product2-Chloro-6-propylimidazo[1,2-b]pyridazine-3-sulfonyl chlorideHCID 23028105—

Reaction Steps

2-Chloro-6-n-propylimidazo[1,2-b]pyridazine (5.00 g, 25.6 mmol) was dissolved in 1,2-dichloroethane (30.0 ml), and chlorosulfonic acid (3.40 ml, 51.1 mmol) was added to the solution at room temperature. The mixture was heated for 8.5 hours under reflux, and then cooled to room temperature, and triethylamine (7.84 ml, 56.2 mmol) and phosphorus oxychloride (5.24 ml, 56.2 mmol) were added thereto and heated for 4 hours under reflux. Cold water was added to the reaction mixture which was then extracted with chloroform. The extracts were combined, dried over anhydrous magnesium sulfate, filtered and concentrated. The concentrated residues were purified by silica gel column chromatography (ethyl acetate:hexane=3:7) to give the title compound as pale yellow crystals. The yield was 7.40 g (98.4%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399381B2
Source datasetuspto-grants-2013_03
ORD IDord-b87c22d4acef486a9760aa24b36c5e57
Source noteuspto-grants-2013_03