HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Chloroaniline → 4-[(3-Chlorophenyl)amino]-6,7-dimethoxyquinoline-3-carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Chloroaniline | HCID 7932 | — |
| Reactant | 1-Ethoxyethanol | HCID 10129898 | — |
| Reactant | 4-Chloro-6,7-dimethoxy-quinoline-3-carbonitrile | HCID 10586676 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 4-[(3-Chlorophenyl)amino]-6,7-dimethoxyquinoline-3-carbonitrile | HCID 5328841 | 54.2% |
Reaction Steps
A mixture of 0.5 g of 4-chloro-6,7-dimethoxy-3-quinolinecarbonitrile, 0.51 g of 3-chloroaniline, 0.16 ml of pyridine, and 6 ml of ethoxyethanol was stirred under nitrogen, at reflux temperature for 6 h. The mixture was cooled and partitioned with dichloromethane and aqueous sodium bicarbonate. The organic layer was washed with water, dried and evaporated. The residue was recrystallized from ethyl acetate-hexanes to give 0.37 g of 4-[(3-chlorophenyl)amino]-6,7-dimethoxy-3-quinolinecarbonitrile as a solid, mp 214-217° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06384051B1 |
| Source dataset | uspto-grants-2002_05 |
| ORD ID | ord-ad3267a056a049898c1d0b40902e8dab |
| Source note | uspto-grants-2002_05 |