HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Bromoaniline → 4-[(3-Bromophenyl)amino]-7-methoxy-3-quinolinecarbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Bromoaniline | HCID 11562 | — |
| Reactant | 4-Chloro-7-methoxyquinoline-3-carbonitrile | HCID 12559431 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | 1-Methoxyethanol | HCID 3015637 | — |
| Product | 4-[(3-Bromophenyl)amino]-7-methoxy-3-quinolinecarbonitrile | HCID 9950460 | 33.2% |
Reaction Steps
A solution of 2.97 g (13.6 mmol) of 4-chloro-7-methoxy -3-quinolinecarbonitrile and 4.67 g (27.2 mmol) of 3-bromo aniline in 76 ml of methoxyethanol was refluxed under nitrogen for 5 hours. The solution was cooled and diluted with ether. Solid was collected and washed with ether. The solid was stirred with a hot mixture of ethyl acetate and sodium bicarbonate solution. The organic layer was separated and dried over magnesium sulfate. Solvent was removed and the residue was recrystallized from a chloroform-ethyl acetate mixture giving 1.6 g of 4-[(3-bromophenyl)amino]-7-methoxy -3-quinolinecarbonitrile as a white solid: mass spectrum (electrospray, m/e): M+H 354.1, 356.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06002008 |
| Source dataset | uspto-grants-1999_12 |
| ORD ID | ord-59ffee7b07164362ab31539418cb1600 |
| Source note | uspto-grants-1999_12 |