HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetaldehyde → HCID 15462583, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetaldehyde | HCID 177 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 18691101 | HCID 18691101 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 15462583 | HCID 15462583 | — |
Reaction Steps
To a solution of 5 g of 3-amino-9-methoxy-2-(2-methylphenyl)imidazo[2,1-a]isoquinoline (Compound 26) in 100 ml of ethanol was added 3.0 ml of acetaldehyde, and the mixture was stirred at room temperature for 3 hours. After 3.3 g of sodium borohydride was added to the mixture and refluxed for 2 hours, the reaction mixture was poured into water, and extracted with ethyl acetate. The extract was washed with saturated saline, and dried over anhydrous magnesium sulfate. The drying agent was removed by filtration, and the solvent was removed under reduced pressure. The crude crystal was recrystallized from petroleum ether/ethyl acetate to give 5 g of the title compound as colorless needles.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06020342 |
| Source dataset | uspto-grants-2000_02 |
| ORD ID | ord-df76ea333494400fb922dba166419447 |
| Source note | uspto-grants-2000_02 |