HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Bromoaniline → HCID 18548941, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Bromoaniline | HCID 11562 | — |
| Reactant | 4,6-Dichloro-1,7-naphthyridine-3-carbonitrile | HCID 18548961 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 18548941 | HCID 18548941 | — |
Reaction Steps
To the above 600 mg of 4,6-dichloro-[1.7]naphthyridine-3-carbonitrile in 20 mL of absolute ethanol was added 1 mL of 3-bromoaniline. After refluxing the reaction under an inert atmosphere for 4 hours, the reaction mixture was cooled to ambient temperature, diluted with ether, and the product was filtered and washed with ether. Drying in vacuo yielded 790 mg of 4-(3-bromo-phenylamino)-6-chloro-[1.7]naphthyridine-3-carbonitrile as an off-white solid: mp=220-223° C.; mass spectrum (m/e): M+H 359.0, 361.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06355636B1 |
| Source dataset | uspto-grants-2002_03 |
| ORD ID | ord-453d6e198bc24996bb23486f5aefab8c |
| Source note | uspto-grants-2002_03 |