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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Chlorosulfonic acid | HCID 24638 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | 2-Chloro-6-propylimidazo[1,2-b]pyridazine | HCID 23028095 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Chloro-6-propylimidazo[1,2-b]pyridazine-3-sulfonyl chloride | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07816526B2 |
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| Source dataset | uspto-grants-2010_10 |
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| ORD ID | ord-2da751994763486a944bf1e666f8bb92 |
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| Source note | uspto-grants-2010_10 |
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