HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 465946Generated: October 27, 2026
Dimethylformamide → 3-Chloro-6-[(2,2-dimethyl-3-sulfamoylpropyl)oxy]imidazo[1,2-b]pyridazine
https://huagongshe.com/reaction/465946
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Imidazo(1,2-b)pyridazine, 6-chloro- | HCID 138828 | — |
| Reactant | 3-Hydroxy-2,2-dimethylpropane-1-sulfonamide | HCID 10329687 | — |
| Product | 3-Chloro-6-[(2,2-dimethyl-3-sulfamoylpropyl)oxy]imidazo[1,2-b]pyridazine | HCID 10829407 | — |
Reaction Steps
To a solution of 1.67 g of 3-hydroxy-2,2-dimethyl-1-propanesulfonamide in 30 ml of DMF was added 0.8 g of sodium hydride, followed by heating at 70° C. for an hour. The mixture to which 1.88 g of 6-chloroimidazo [1,2-b]pyridazine was added was heated for 4.5 hours. The reaction mixture was distilled to remove the solvent under reduced pressure and 50 ml of ice-water was added to the residue. The mixture was adjusted to pH 6.0 with 1N-hydrochloric acid and then extracted with tetrahydrofuran and ethyl acetate (1:1). The extract was dried over anhydrous magnesium sulfate and distilled under reduced pressure to remove the solvent. The residue was subjected to a silica gel column chromatography, eluting with chloroform and methanol (20:1). The corresponding combined fractions were concentrated to obtain 1.56 g of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05155108 |
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| Source dataset | uspto-grants-1992_10 |
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| ORD ID | ord-239318e44645457da53e21c864e72c8e |
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| Source note | uspto-grants-1992_10 |
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