Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 9926492 | HCID 9926492 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 12968335 | HCID 12968335 | — |
Reaction Steps
6-Amino-3-(4-pyridyl)-2-(4-fluorophenyl)-7-aza-indole (17) (50 mg, 0.164 mmol) and acetic anhydride (0.5 mL) were warmed to 60° C. for 1 h. After cooling to 23° C., the reaction was diluted with ethyl acetate (50 mL), washed with NaOH (1 N, 50 mL), and dried (Na2SO4). Concentration in vacuo afforded 6-(1′-oxo-ethylamino)-3-(4-pyridyl)-2-(4-fluorophenyl)-7-aza-indole (57): Mass Spectrum (CI) 347 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06440973B1 |
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| Source dataset | uspto-grants-2002_08 |
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| ORD ID | ord-932801ccc82c4e19bd1d53787999004a |
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| Source note | uspto-grants-2002_08 |
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