HuagongsheHuagongshe Chemistry Print Report · For research reference only
Aminopyridazine → (1-Imidazo[1,2-b]pyridazin-2-yl-ethyl)-carbamic acid benzyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Aminopyridazine | HCID 230373 | — |
| Reactant | Benzyl (4-bromo-3-oxobutan-2-yl)carbamate | HCID 73196234 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | (1-Imidazo[1,2-b]pyridazin-2-yl-ethyl)-carbamic acid benzyl ester | HCID 67433032 | — |
Reaction Steps
A mixture of pyridazin-3-ylamine (2 g, 21.05 mmol) and (3-bromo-1-methyl-2-oxopropyl)-carbamic acid benzyl ester (7.5 g, 25.26 mmol) in EtOH (25 mL) was heated to reflux overnight. After completion, the reaction mixture was cooled to rt. EtOH was removed in vacuo. The residue was dissolved in EtOAc. The organic layer was dried over sodium sulfate, filtered and concentrated in vacuo. The crude product was purified by column chromatography using silica gel (100-200 mesh) and 0-5% MeOH in DCM to provide (1-imidazo[1,2-b]pyridazin-2-yl-ethyl)-carbamic acid benzyl ester: LC-MS (ESI) m/z 297.3 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08575183B2 |
| Source dataset | uspto-grants-2013_11 |
| ORD ID | ord-39e76ec047ac4006adff339bc5247f70 |
| Source note | uspto-grants-2013_11 |