Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 69347098 | HCID 69347098 | — |
| Product | HCID 22139754 | HCID 22139754 | 22.2% |
Reaction Steps
5-(2,4-Difluoro-phenoxy)-6-methoxy-quinoline N-oxide (1.35 g, 4.5 mmol) was mixed with 5 mL of acetic anhydride and stirred at 75° C. for 22 hours. The reaction mixture was poured on ice, neutralized with aqueous ammonia, and the resultant precipitate was filtered and washed with water. The aqueous layer was extracted with dichloromethane and the organic extract was dried over MgSO4. The solvent was removed under vacuum. The dry residue, combined with the filtered precipitate, was dissolved in a minimum amount of CH2Cl2 and purified using a Biotage system, eluting with 10–30% EtOAc/hexane to give 0.3 g (22.2%) of 5-(2,4-difluoro-phenoxy)-6-methoxy-1H-quinolin-2-one.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07049325B2 |
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| Source dataset | uspto-grants-2006_05 |
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| ORD ID | ord-5c0d953df7204b5f962a72f5bea0d979 |
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| Source note | uspto-grants-2006_05 |
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