Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia methanol | HCID 21705897 | — |
| Reactant | HCID 66730448 | HCID 66730448 | — |
| Product | HCID 46940875 | HCID 46940875 | 56% |
Reaction Steps
Ethyl 8-(3-fluoro-4-hydroxyphenyl)-1,6-naphthyridine-2-carboxylate (100 mg, 0.32 mmol) synthesized in Example 1 (1a) was dissolved in a 7M ammonia-methanol solution (10 mL), followed by stirring while heating at 80° C. for three hours. After cooling the resulting reaction liquid to room temperature, a precipitated solid was collected by filtration to give the desired title compound (51 mg, yield 56%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08410273B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-12927331ae2b45e084c81837eae7f38d |
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| Source note | uspto-grants-2013_04 |
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