HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → {3-Methyl-4-[3-(3-nitroimidazo[1,2-b]pyridazin-6-ylsulfanyl)propoxy]pyridin-2-yl}-methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | [4-(3-Chloropropoxy)-3-methylpyridin-2-yl]methanol | HCID 18799386 | — |
| Reactant | HCID 178526776 | HCID 178526776 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | {3-Methyl-4-[3-(3-nitroimidazo[1,2-b]pyridazin-6-ylsulfanyl)propoxy]pyridin-2-yl}-methanol | HCID 18799407 | 69.5% |
Reaction Steps
570 mg (2.9 mmol) of 3-nitroimidazo[1,2-b]pyridazine-6-thiol, 500 mg (2.3 mmol) of [4-(3-chloropropoxy)-3-methylpyridin-2-yl]methanol and 0.4 ml (2.9 mmol) of triethylamine in 10 ml of dimethylformamide are heated to 100° C for 1 h under a nitrogen atmosphere. After cooling to room temperature, water (100 ml) is added and the mixture is extracted with 3×50 ml of ethyl acetate. The residual oil is crystallized from methanol. 600 mg (69%) of the title compound are isolated as a pale beige solid. M.p. 135-136° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06043242 |
| Source dataset | uspto-grants-2000_03 |
| ORD ID | ord-a634cd2913824daab541310d657f2fc2 |
| Source note | uspto-grants-2000_03 |