HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Naphthylamine → (6,7-Dimethoxy-quinazolin-4-yl)-alpha-naphthalenylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Naphthylamine | HCID 8640 | — |
| Reactant | 4-Chloro-6,7-dimethoxyquinazoline | HCID 2769364 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | (6,7-Dimethoxy-quinazolin-4-yl)-alpha-naphthalenylamine | HCID 18770835 | — |
Reaction Steps
To a 25 mL flask with 10 ml of abs. EtOH is added 0.137 g of 4-chloro-6,7-dimethoxyquinazoline and 0.087 g of 1-aminonaphthalene. The solution is heated to reflux whereupon the insoluble materials dissolve. After 5 minutes at reflux a precipitate forms. The solution is allowed to stir an additional 10 minutes before cooling and isolation of the product as the hydrochloride salt by simple filtration. High-vacuum drying of the solid provided analytically pure (6,7-dimethoxy-quinazolin-4-yl)-alpha-naphthalenylamine (0.142 g, white powder, m.p. 271-273° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06057320 |
| Source dataset | uspto-grants-2000_05 |
| ORD ID | ord-0cbd15fe954d43929611d77f9de1bf82 |
| Source note | uspto-grants-2000_05 |