HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Ethyl-6,8-dimethyl-3-hydroxymethylimidazo[1,2-b]pyridazine → 2-Ethyl-6,8-dimethylimidazo[1,2-b]pyridazin-3-carboxaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Ethyl-6,8-dimethyl-3-hydroxymethylimidazo[1,2-b]pyridazine | HCID 19784143 | — |
| Reactant | Ethyl acetate hexane | HCID 21226206 | — |
| Catalyst | HCID 178418406 | HCID 178418406 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Ethyl-6,8-dimethylimidazo[1,2-b]pyridazin-3-carboxaldehyde | HCID 19784156 | 89% |
Reaction Steps
To a solution of 0.886 g (4.32 mmol) of the product of Step B dissolved in 15 mL of CH2Cl2 was added 1.772 g of powdered 4A molecular sieves and 4.430 g (51 mmol) of manganese dioxide and the reaction mixture was magnetically stirred at room temperature. After 16 h, TLC analysis (50% EtOAc-hexane) indicated complete reaction and the mixture was filtered. The filtrate was concentrated in vacuo, and the residue was redissolved in 50% EtOAc-hexane and purified by filtration through a short plug of silica gel. Evaporation of the filtrate and drying in vacuo afforded 0.781 g (89%) of the title compound as a tan solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05250521 |
| Source dataset | uspto-grants-1993_10 |
| ORD ID | ord-7f949234e4d8453a9ec27b42d3e5799f |
| Source note | uspto-grants-1993_10 |