HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → 3-Benzoyl-4-(2-methoxyphenylamino)-8-methoxyquinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 3-Benzoyl-4-chloro-8-methoxyquinoline | HCID 10086018 | — |
| Solvent | 2-Methoxyaniline | HCID 7000 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 3-Benzoyl-4-(2-methoxyphenylamino)-8-methoxyquinoline | HCID 21274558 | 61% |
Reaction Steps
3-Benzoyl-4-chloro-8-methoxyquinoline (2.8 g, 0.0094 mol) was heated under reflux in a mixture of 1,4-dioxan (50 ml) and o-anisidine (7 ml) for 1 hour. The solvent was evaporated and the residue was dissolved in dichloromethane, and washed with dilute hydrochloric acid sodium hydrogen carbonate solution, water and brine. The organic solution was dried and evaporated to an oil which was chromatographed (silica gel, 1% methanol in dichloromethane) to give an oil which afforded yellow crystals of 3-benzoyl-4-(2-methoxyphenylamino)-8-methoxyquinoline (2.2 g, 61%) from ethyl acetate, m.p. 200°-202°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04806549 |
| Source dataset | uspto-grants-1989_02 |
| ORD ID | ord-065ba7747cde4426948af7c4ab166be0 |
| Source note | uspto-grants-1989_02 |