Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 4-Methoxybenzoic Acid | HCID 7478 | — |
| Reactant | HCID 13787376 | HCID 13787376 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 13787391 | HCID 13787391 | 41% |
Reaction Steps
The procedure is analogous to that described in Example 1, but starting with 4-methoxybenzoic acid (6.1 g), N,N'-carbonyldiimidazole (6.5 g) and 2-amino-7-anilino-1,8-naphthyridine (7 g). The product obtained by precipitation in water (12 g) is dissolved in boiling ethanol (140 cc). After cooling for 1 hour at 4° C., the crystallized solid is separated by filtration, washed with ethanol (10 cc), and dried at 45° C. under reduced pressure (0.07 kPa). N-(7-Anilino-1,8-naphthyridin-2-yl)-4-methoxybenzamide (4.5 g), m.p. 245° 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-5a797eaf26f74792a71249d689b533c1 |
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| Source note | uspto-grants-1988_01 |
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