Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Benzylamine | HCID 7504 | — |
| Reactant | HCID 22346370 | HCID 22346370 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 22346251 | HCID 22346251 | — |
Reaction Steps
Dimethyl 8-(benzoyloxy)-1,6-naphthyridine-5,7-dicarboxylate (2.0 g, 5.46 mmol, prepared as in Example 164) was dissolved in dry methanol (4.0 ml) in a pressure tube. Benzylamine (0.58 g, 5.46 mmol) was added and the reaction capped and heated to 80 degrees C. under nitrogen for 16 hours. LCMS analysis indicated that the reaction was complete. The reaction was transferred to an Erlenmeyer flask and then diethyl ether was added to precipitate the product. Filtered and dried the solid in vacuo to obtain the desired compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06921759B2 |
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| Source dataset | uspto-grants-2005_07 |
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| ORD ID | ord-1462e95fc82245ee813d63d36e635df1 |
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| Source note | uspto-grants-2005_07 |
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