HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Toluenesulfonic acid → Methyl 4-(8-bromoimidazo[1,2-b]pyridazin-6-yl)benzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 2-Chloro-1,1-diethoxyethane | HCID 12128 | — |
| Reactant | Methyl 4-(6-amino-5-bromopyridazin-3-yl)benzoate | HCID 86682705 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | Methyl 4-(8-bromoimidazo[1,2-b]pyridazin-6-yl)benzoate | HCID 86682706 | 36.2% |
Reaction Steps
A solution of methyl 4-(6-amino-5-bromopyridazin-3-yl)benzoate (1.64 g, 5.32 mmol), 2-chloro-1,1-diethoxyethane (0.984 g, 6.39 mmol) and PTSA (1.215 g, 6.39 mmol) in isopropanol (50 mL) was heated to 80° C. for 40 h. After cooling to room temperature, the solution was concentrated in vacuo. The resulting mixture was treated with a saturated NaHCO3 solution (50 mL), extracted with dichloromethane (50 mL×3), dried over Na2SO4, filtered and concentrated. The residue was purified by chromatography (silica gel, 200-300 mesh, petroleum ether:ethyl acetate=3:1) to give methyl 4-(8-bromoimidazo[1,2-b]pyridazin-6-yl)benzoate (640 mg, 36%) as a white solid. LC-MS: [M+H]+, 333.9, tR=1.637 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09169259B2 |
| Source dataset | uspto-grants-2015_10 |
| ORD ID | ord-adab5625d3314637a6929b3b18ce328b |
| Source note | uspto-grants-2015_10 |