Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Propanol | HCID 1031 | — |
| Reactant | 3-Bromobenzoic acid | HCID 11456 | — |
| Reactant | HCID 13983423 | HCID 13983423 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 13983440 | HCID 13983440 | 56.9% |
Reaction Steps
The procedure is analogous to that described in Example 11, but starting with 3-bromobenzoic acid (2.2 g), N,N'-carbonyldiimidazole (1.8 g) and 2-amino-7-(3-bromophenyl)-1,8-naphthyridine (2.4 g). The product obtained by precipitation in water (3.1 g; m.p. approximately 140° C.) is dissolved in boiling propanol (100 cc). After cooling for 3 hours at 4° C., the crystallized solid is separated by filtration, washed with propanol (2×10 cc) and dried at 40° C. under reduced pressure (0.07 kPa). N-[7-(3-Bromophenyl)-1,8-naphthyridin-2-yl]-3-bromobenzamide (2.2 g), m.p. 144°-146° 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-789f7c73468640b781de45787b959e37 |
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| Source note | uspto-grants-1988_01 |
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