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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1160759Generated: October 26, 2026

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

https://huagongshe.com/reaction/1160759

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 numberUS07816526B2
Source datasetuspto-grants-2010_10
ORD IDord-2da751994763486a944bf1e666f8bb92
Source noteuspto-grants-2010_10