Potassium Hydroxide → 4-Methyl-2,3-dihydro-1H-pyrrolo[2,3-b]pyridine
Reaktionsgleichung
[OH-].[K+].C([N:6]1[C:14]2[C:9](=[C:10]([CH3:15])[CH:11]=[CH:12][N:13]=2)[CH2:8][CH2:7]1)(=O)C>CO>[CH3:15][C:10]1[CH:11]=[CH:12][N:13]=[C:14]2[C:9]=1[CH2:8][CH2:7][NH:6]2Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 55 °C
Versuchsvorschrift
Potassium hydroxide (1 M, 5 mL) was added to a stirred solution of N-acetyl-4-methyl-7-azaindoline (0.78 g, 4.75 mmol) in methanol (10 mL) and the resulting mixture was heated to 55° C. for 4 h. The mixture was cooled and partitioned between methylene chloride and dilute ammonium hydroxide solution. The organic layer was dried (Na2SO4) and evaporated in vacuo to give the title compound as a yellow solid:
Aufarbeitung
- temperatureThe mixture was cooled
- custompartitioned between methylene chloride and dilute ammonium hydroxide solution
- dry with materialThe organic layer was dried (Na2SO4)
- customevaporated in vacuo
Quellen und Nachweise
- ORD-Eintrag
- ord-1f9dde4644eb4a3898903e086b7d9995
- Quelldatensatz
- uspto-grants-2003_08
- Patentnummer
- US06610692B1
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