HuagongsheHuagongshe Chemistry Print Report · For research reference only
6-[3-(2-Chloromethyl-3-methylpyridin-4-ylsulfanyl)propylsulfanyl]-3-nitroimidazo[1,2-b]pyridazine → 6-{3-[2-(1H-benzimidazol-2-ylsulfanylmethyl)-3-methylpyridin-4-ylsulfanyl]propylsulfanyl}-3-nitroimidazo[1,2-b]pyridazine hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 6-[3-(2-Chloromethyl-3-methylpyridin-4-ylsulfanyl)propylsulfanyl]-3-nitroimidazo[1,2-b]pyridazine | HCID 18799383 | — |
| Reactant | HCID 178527775 | HCID 178527775 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | 6-{3-[2-(1H-benzimidazol-2-ylsulfanylmethyl)-3-methylpyridin-4-ylsulfanyl]propylsulfanyl}-3-nitroimidazo[1,2-b]pyridazine hydrochloride | HCID 18799420 | 86.4% |
Reaction Steps
A suspension of 6-[3-(2-chloromethyl-3-methylpyridin-4-ylsulfanyl)propylsulfanyl]-3-nitroimidazo[1,2-b]pyrid-azine (0.39 g, 0.95 mmol) and 2-mercapto-1H-benzimidazole (160 mg, 1.05 mmol) in isopropanol (50 ml) is heated under reflux for 7 h. After cooling to room temperature, the precipitate is filtered off, washed with isopropanol and dried at 40° C. in vacuo. The title compound (0.46 g, 86%) is isolated as a beige solid. M.p. 200-207° C (dec.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06043242 |
| Source dataset | uspto-grants-2000_03 |
| ORD ID | ord-2ea89ee7ae65441f99af13d320435e22 |
| Source note | uspto-grants-2000_03 |