HuagongsheHuagongshe Chemistry Print Report · For research reference only
P-Anisidine → HCID 23209265, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | P-Anisidine | HCID 7732 | — |
| Reactant | 3,8-dichloro-1,5-naphthyridine | HCID 607822 | — |
| Product | HCID 23209265 | HCID 23209265 | — |
Reaction Steps
A mixture of 4,7-dichloro-1,5-naphthyridine (0.65 g), 4-methoxyaniline (0.40 g) and IMS (25 ml) was boiled under reflux for 5 hours. The mixture was concentrated to approximately 5 ml and then ether added to induce precipitation. Ethyl acetate was added and the solid was collected by filtration to give 7-chloro-4-(4-methoxyanilino)-1,5-naphthyridine hydrochloride hydrate m.p. 230°-233° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05780482 |
| Source dataset | uspto-grants-1998_07 |
| ORD ID | ord-43893a38815b4dd0b74492f57d0984a4 |
| Source note | uspto-grants-1998_07 |