Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Aminopyridine | HCID 10439 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 6,8-Dichloroimidazo[1,2-b]pyridazine | HCID 57517539 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 57786669 | HCID 57786669 | 35% |
Reaction Steps
A solution of 2-aminopyridine (0.388 g, 4.12 mmol) in 8 mL of N,N-dimethylformamide was treated with 60% sodium hydride/mineral oil (0.167 g, 4.18 mmol) and the lightly bubbling, pale yellow solution was stirred for 30 min., in which time it became a dark yellow cloudy solution. The solution was added via Pasteur pipette to a flask containing 6,8-dichloro-imidazo[1,2-b]pyridazine (0.310 g, 1.65 mmol), and the cloudy orange solution was stirred for 16 h then partitioned between 80 mL of a saturated aq. NH4Cl solution and 80 mL of ether. The organic layer was sequentially washed with two 40 mL portions of water and 40 mL of a saturated aq. NaCl solution; dried over MgSO4, filtered and concentrated to a pale yellow solid. Column chromatography (0->33% EtOAc/hexanes) afforded 0.141 g (35%) of (6-chloro-imidazo[1,2-b]pyridazin-8-yl)-pyridin-2-yl-amine as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08426441B2 |
|---|
| Source dataset | uspto-grants-2013_04 |
|---|
| ORD ID | ord-552038548e9a4dd5b006d0bd11a6733b |
|---|
| Source note | uspto-grants-2013_04 |
|---|