HuagongsheHuagongshe Chemistry Print Report · For research reference only
Imidazo(1,2-b)pyridazine, 6-chloro- → 6-[(3-Sulfamoyl-2,2-dimethylpropyl)thio]imidazo[1,2-b]pyridazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Imidazo(1,2-b)pyridazine, 6-chloro- | HCID 138828 | — |
| Reactant | 3-Mercapto-2,2-dimethyl-1-propylsulfonamide | HCID 10464982 | — |
| Reactant | Sodium methanolate methanol | HCID 23694274 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 6-[(3-Sulfamoyl-2,2-dimethylpropyl)thio]imidazo[1,2-b]pyridazine | HCID 9972030 | 66% |
Reaction Steps
To a solution of 0.37 g of 3-mercapto-2,2-dimethyl-1-propylsulfonamide and 0.37 g of 28% sodium methoxide-methanol solution in 50 ml of methanol was added 0.31 g of 6-chloroimidazo[1,2-b]pyridazine, followed by refluxing at 80°-85° C. for 3 hours. The reaction solution was concentrated under reduced pressure. The residue to which 30 ml of water were added was 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 recrystallized from ethanol to obtain 0.4 g of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05155108 |
| Source dataset | uspto-grants-1992_10 |
| ORD ID | ord-adc395e2f36341b8a96f5d1ee8e1d9d7 |
| Source note | uspto-grants-1992_10 |