HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloroacetaldehyde → 6-Chloro-7-methylimidazo[1,2-b]pyridazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloroacetaldehyde | HCID 33 | — |
| Reactant | 6-Chloro-5-methylpyridazin-3-amine | HCID 12353663 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | 6-Chloro-7-methylimidazo[1,2-b]pyridazine | HCID 12248336 | 33.4% |
Reaction Steps
6-chloro-5-methylpyridazin-3-amine 7 (0.6 g, 4.18 mmol) was dissolved in n-butanol (10 ml) and chloroacetaldehyde (0.328 g, 4.18 mmol) was added. The reaction was refluxed for 6 hrs and n-butanol was removed under reduced pressure. The crude product was purified by column chromatography (DCM/hexane, 70:30) to afford compound 8 (0.234 g, yield=33.4%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08710057B2 |
| Source dataset | uspto-grants-2014_04 |
| ORD ID | ord-628d679f24a04e08b2af763659ac6b14 |
| Source note | uspto-grants-2014_04 |