Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 21936644 | HCID 21936644 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 21936635 | HCID 21936635 | 100% |
Reaction Steps
A mixture of 1-(3-nitrophenyl)-3-[3-hydroxy-3-(pyridin-4-yl)propyl]-1,8-naphthyridin-2(1H)-one (50 mg, 0.12 mmol; prepared in Example 20) in acetic anhydride (0.2 ml) and pyridine (0.3 ml) was heated at 100° C. for 20 min, concentrated, and extracted with chloroform. The extract was treated according to conventional techniques, concentrated, and then purified by flash column chromatography to afford 1-(3-nitrophenyl)-3-[3-acetyloxy-3-(pyridin-4-yl)propyl]-1,8-naphthyridin-2(1H)-one (55.2 mg, 100%; mp 69–71° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07115623B2 |
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| Source dataset | uspto-grants-2006_10 |
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| ORD ID | ord-6147352068f74fabaf8b055cf2fe14e4 |
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| Source note | uspto-grants-2006_10 |
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