Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Aniline | HCID 6115 | — |
| Reactant | 7-Chloro-1,8-naphthyridin-2-amine | HCID 85199 | — |
| Product | HCID 13787376 | HCID 13787376 | 60.8% |
Reaction Steps
A suspension of 2-amino-7-chloro-1,8-naphthyridine (9 g) in aniline (19.6 g) is heated for 19 hours at 120° C. The suspension obtained is filtered, washed with diethyl ether (3×15 cc) and air-dried. The crude solid obtained (14 g; m.p. 190° C.) is then dissolved in boiling ethanol (700 cc). After cooling for 2 hours at 4° C., the crystallized product is separated by filtration, washed with ethanol (25 cc) and air-dried. 2-Amino-7-anilino-1,8-naphthyridine (7.2 g), m.p. approximately 250° C., is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04720500 |
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| Source dataset | uspto-grants-1988_01 |
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| ORD ID | ord-e62183325161482e973bedeb87b2864c |
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| Source note | uspto-grants-1988_01 |
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