HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → [6-(6-Chloro-imidazo[1,2-b]pyridazin-8-ylamino)-pyridin-3-yl]-morpholin-4-yl-methanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 8-Bromo-6-chloroimidazo(1,2-b)pyridazine | HCID 46835269 | — |
| Reactant | (6-Aminopyridin-3-yl)(morpholino)methanone | HCID 59259223 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | [6-(6-Chloro-imidazo[1,2-b]pyridazin-8-ylamino)-pyridin-3-yl]-morpholin-4-yl-methanone | HCID 57786785 | 100.1% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
A mixture of 8-bromo-6-chloroimidazo[1,2-b]pyridazine (272 mg, 1.17 mmol, Eq: 1.00) and (6-aminopyridin-3-yl)(morpholino)methanone (255 mg, 1.23 mmol, Eq: 1.05) in DMF (10.0 ml) was cooled to 0° C. To this reaction mixture was added sodium hydride (150 mg, (60% in mineral oil), 3.74 mmol, Eq: 3.2). The reaction was allowed to stir at 0° C. for 10 minutes and then allowed to warm to room temperature and stir 18 h. The reaction mixture was quenched with sat. NaHCO3 (aq) and diluted with water and EtOAc. An insoluble solid was collected by filtration to give [6-(6-chloro-imidazo[1,2-b]pyridazin-8-ylamino)-pyridin-3-yl]-morpholin-4-yl-methanone (420 mg, 99%). LC/MS-ESI observed [M+H]+ 358.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08742098B2 |
| Source dataset | uspto-grants-2014_06 |
| ORD ID | ord-d3dbf29455954ae3a7d53f501695c330 |
| Source note | uspto-grants-2014_06 |