Sodium hydride → 6-chloro-1-(cyano-methyl-methyl)-1H-indole-2-carboxylic acid ethyl ester
Reaktionsgleichung
[H-].[Na+].[CH2:3]([O:5][C:6]([C:8]1[NH:9][C:10]2[C:15]([CH:16]=1)=[CH:14][CH:13]=[C:12]([Cl:17])[CH:11]=2)=[O:7])[CH3:4].Br[CH:19]([CH3:22])[C:20]#[N:21]>CN(C)C=O>[CH2:3]([O:5][C:6]([C:8]1[N:9]([CH:19]([C:20]#[N:21])[CH3:22])[C:10]2[C:15]([CH:16]=1)=[CH:14][CH:13]=[C:12]([Cl:17])[CH:11]=2)=[O:7])[CH3:4]Komponenten
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 0 °C
Versuchsvorschrift
Sodiumhydride (0.89 g, 20.1 mmol) was suspended in dimethylformamide (15 mL) and a solution of 6-chloro-1H-indole-2-carboxylic acid ethyl ester (2.00 g, 8.9 mmol) in dimethylformamide (8 mL) was added at 0° C. The mixture was stirred for 1 h at 0° C. then 2-bromo-propionitrile (3.6 g, 23.95 mmol) was added. After 1 h at room temperature the mixture was heated at 75° C. for 18 hours. The reaction mixture was then added to an ice/water mixture (100 mL) and extracted with ethylacetate. The organic phases were pooled washed with brine, dried with Na2SO4 and the solvent was removed in vacuo. Chromatography on silica gel (ether/n-hexane 1:4) yielded 6-chloro-1-(cyano-methyl-methyl)-1H-indole-2-carboxylic acid ethyl ester (2.06 g, 67%) as a colorless solid, MS: m/e=277.2 (M+H+).
Aufarbeitung
- temperatureAfter 1 h at room temperature the mixture was heated at 75° C. for 18 hours
- extractionextracted with ethylacetate
- washThe organic phases were pooled washed with brine
- dry with materialdried with Na2SO4
- customthe solvent was removed in vacuo
Quellen und Nachweise
- ORD-Eintrag
- ord-51b73faeda354cc4b2ede80b96b61208
- Quelldatensatz
- uspto-grants-2007_08
- Patentnummer
- US07253281B2
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