Water → 2-ethyl-5-fluoro-1H-indole
Reaktionsgleichung
[C:1]([C:5]1[CH:10]=[C:9]([F:11])[CH:8]=[CH:7][C:6]=1[NH2:12])#[C:2][CH2:3][CH3:4].O>CN1CCCC1=O>[CH2:3]([C:2]1[NH:12][C:6]2[C:5]([CH:1]=1)=[CH:10][C:9]([F:11])=[CH:8][CH:7]=2)[CH3:4]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
Under argon 4.9 g potassium-tert-butoxide are suspended in 25 ml N-methyl-2-pyrrolidinone and a suspension of 3.4 g 2-but-1-ynyl-4-fluorophenylamine in 25 ml N-methyl-2-pyrrolidinone is added dropwise thereto. The reaction mixture is stirred for 3 hours at ambient temperature and mixed with water. The product is extracted with diethyl ether and purified by chromatography (silica gel, cyclohexane/ethyl acetate 100/0-90/10). 2.83 g product are obtained in the form of a solid. 1H NMR (400 MHz, DMSO): 2.72 (2H, q); 1.27 (3H, t).
Aufarbeitung
- additionis added dropwise
- extractionThe product is extracted with diethyl ether
- custompurified by chromatography (silica gel, cyclohexane/ethyl acetate 100/0-90/10)
Quellen und Nachweise
- ORD-Eintrag
- ord-0d0c4b3599d04e63a7999c9a64a9e5f7
- Quelldatensatz
- uspto-grants-2015_10
- Patentnummer
- US09161927B2
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