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-[3-Methyl-2-(pyridin-4-ylsulfanylmethyl)-pyridin-4-ylsulfanyl]propylsulfanyl}-3-nitro-imidazo[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 | pyridine-4-thiol | HCID 178418431 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | 6-{3-[3-Methyl-2-(pyridin-4-ylsulfanylmethyl)-pyridin-4-ylsulfanyl]propylsulfanyl}-3-nitro-imidazo[1,2-b]pyridazine hydrochloride | HCID 70272292 | 87.1% |
Reaction Steps
0.53 g (1.3 mmol) of 6-[3-(2-chloromethyl-3-methylpyridin-4-ylsulfanyl)propylsulfanyl]-3-nitro-imidazo[1,2-b]pyridazine and 0.15 g (1.3 mmol) of 4-mercaptopyridine in 30 ml of isopropanol are reacted as described in Example 2. 0.59 g (87%) of the title compound of m.p. 174-178° C. is isolated.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06043242 |
| Source dataset | uspto-grants-2000_03 |
| ORD ID | ord-75c605af579649edb505f05da2c41d4b |
| Source note | uspto-grants-2000_03 |