HuagongsheHuagongshe Chemistry Print Report · For research reference only
O-Methylhydroxylamine hydrochloride → HCID 67506760, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | O-Methylhydroxylamine hydrochloride | HCID 521874 | — |
| Reactant | HCID 57853761 | HCID 57853761 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 67506760 | HCID 67506760 | 86.7% |
Reaction Steps
O-methylhydroxylamine hydrochloride (1.51 g, 1.7 eq) was added to a solution of N-(4-chloroquinolin-3-yl)propionamide (2.5 g, 1.0 eq) in ethanol (75 mL). The reaction mixture was heated at reflux for 3 hours, cooled to ambient temperature, and then concentrated under reduced pressure. The residue was partitioned between dichloromethane and aqueous saturated sodium bicarbonate. The organic layer was separated and concentrated under reduced pressure to provide 2.10 g of 2-ethyl-1-methoxy-1H-imidazo[4,5-c]quinoline as a brown solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07579359B2 |
| Source dataset | uspto-grants-2009_08 |
| ORD ID | ord-a1e8f7ad1d4a4dee853d0b9838e6686f |
| Source note | uspto-grants-2009_08 |