Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Succinic anhydride | HCID 7922 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | N1-cyclopropyl-5-((2-amino-4-pyridyl)oxy)-1H-1-indolecarboxamide | HCID 21949236 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 22936416 | HCID 22936416 | — |
Reaction Steps
N1-Cyclopropyl-5-[(2-amino-4-pyridyl)oxy]-1H-1-indolecarboxamide (830 mg), succinic anhydride (270 mg) and toluene (30 ml) were refluxed together for 30 minutes. After adding 50 ml of acetic anhydride and 82 mg of sodium acetate to the reaction solution, the mixture was stirred at 80° C. for 15 minutes. The solvent was distilled off under reduced pressure, and the residue was purified by silica gel chromatography (ethyl acetate). The second eluted substance was N1-cyclopropyl-5-{[2-(2,5-dioxotetrahydro-1H-1-pyrrolyl)-4-pyridyl]oxy}-1H-1-indolecarboxamide, of which 440 mg was obtained as a colorless powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07612092B2 |
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| Source dataset | uspto-grants-2009_11 |
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| ORD ID | ord-02586d11f8874a148c97851a501dcabf |
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| Source note | uspto-grants-2009_11 |
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