HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → Imidazo[1,2-b]pyridazin-3-yl-carbamic acid phenyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Phenyl chloroformate | HCID 15891 | — |
| Reactant | Imidazo[1,2-b]pyridazin-3-amine | HCID 10702308 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Imidazo[1,2-b]pyridazin-3-yl-carbamic acid phenyl ester | HCID 58442681 | 72% |
Reaction Steps
To a solution of imidazo[1,2-b]pyridazin-3-ylamine (209 mg, 1.56 mmol) in dry DMF (5.0 mL) was added pyridine (382 μL, 4.68 mmol) and phenyl chloroformate (244 mg, 1.56 mmol). After 3 h at rt, the mixture was diluted with EtOAc (100 mL) and washed with saturated aqueous NaHCO3 (50 mL). The organic layer was dried (MgSO4) and concentrated. The residue was purified (FCC) to give imidazo[1,2-b]pyridazin-3-yl-carbamic acid phenyl ester (285 mg, 72%). MS (ESI+): calcd for C13H10N4O2 m/z 254.08, found 255.3 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08598356B2 |
| Source dataset | uspto-grants-2013_12 |
| ORD ID | ord-1cada48fa53a4ab0bc24f7868c7b5391 |
| Source note | uspto-grants-2013_12 |