HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Butanone, 3-bromo- → 6-Methyl-8-phenylmethoxy-2,3-dimethylimidazo[1,2-b]pyridazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Butanone, 3-bromo- | HCID 13142 | — |
| Reactant | 3-Amino-6-methyl-4-phenylmethoxypyridazine | HCID 15591911 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 6-Methyl-8-phenylmethoxy-2,3-dimethylimidazo[1,2-b]pyridazine | HCID 15591912 | — |
Reaction Steps
A mixture of (0.01 mole) 3-amino-6-methyl-4-phenylmethoxypyridazine, [prepared following the methodology of Becket, et al. J. Pract. Chem., 311, 285(1969) and references cited therein], and (0.012 mole) 2-bromo-3-butanone in methanol is heated for 24 hours in a bath maintained at 100°. The mixture is cooled to room temperature and partitioned between aqueous sodium bicarbonate and methylene chloride. The layers are separated and the aqueous phase extracted with methylene chloride. The organic extracts are combined and dried over anhydrous sodium sulfate. The solvent is removed under reduced pressure to give 6-methyl-8-phenylmethoxy-2,3-dimethylimidazo[1,2-b]pyridazine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04464372 |
| Source dataset | uspto-grants-1984_08 |
| ORD ID | ord-1717a85a15664a429084898fa46e5458 |
| Source note | uspto-grants-1984_08 |