Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonia | HCID 222 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | 7-Bromo-2-chloro-1,5-naphthyridine | HCID 58310544 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 7-Bromo-1,5-naphthyridin-2-amine | HCID 58310532 | 80% |
Reaction Steps
In a sealed reactor, 500 mg (1.23 mmol, 1 eq) of 7-bromo-2-chloro-1,5-naphthyridine and 7 mL (41.6 mmol, 33 eq) of 20% aqueous ammonia solution were introduced in 7 mL of dioxane. The mixture was stirred at 160° C. for 24 h. The mixture was allowed to reach rt and water was added. Aqueous layer was extracted with ethyl acetate. Organic layers were dried over Na2SO4, filtered and evaporated to dryness. The residue was purified by column chromatography using methylene chloride and then methylene chloride/ethanol: 98/2 as eluent. The solvent was evaporated to dryness to afford 220 mg of white powder with 80% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08461178B2 |
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| Source dataset | uspto-grants-2013_06 |
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| ORD ID | ord-6b8b6c9b669a4c45981c5dbd5658792a |
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| Source note | uspto-grants-2013_06 |
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