Water → 2-(1H-Indol-5-yl)-N-methylethane-1-sulfonamide
Reaktionsgleichung
[CH3:1][NH:2][S:3]([CH2:6][CH2:7][C:8]1[CH:13]=[CH:12][C:11]([NH:14]C(=O)C)=[C:10]([C:18]#[C:19][Si](C)(C)C)[CH:9]=1)(=[O:5])=[O:4].CC(C)([O-])C.[K+].O.CCCCCCC>CN1CCCC1=O>[CH3:1][NH:2][S:3]([CH2:6][CH2:7][C:8]1[CH:9]=[C:10]2[C:11](=[CH:12][CH:13]=1)[NH:14][CH:19]=[CH:18]2)(=[O:4])=[O:5]Komponenten
6
Edukt 4
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 82.5 °C
Versuchsvorschrift
N-[4-(2-methylsulfamoyl-ethyl)-2-trimethylsilanylethynyl-phenyl]-acetamide (100 gm) was dissolved in N-methylpyrrolidone (900 ml) at 25° C. under inert atmosphere. Potassium tert-butoxide (49 g) was added and heated to 80-85° C. for 120-150 minutes. The reaction mass was cooled gradually to 25° C., water (3000 ml) was added and stirred for 30 minutes. The solution was extracted with ethyl acetate (2000 ml). The organic layer was dried over sodium sulfate and vacuum distilled to obtain a residue. The residue was treated with heptane (300 ml) to obtain a solid. The solid was filtered, washed with heptane and dried at 50-55° C. under vacuum to obtain title compound. (Yield: 74 g, HPLC Purity: 98%)
Aufarbeitung
- temperatureThe reaction mass was cooled gradually to 25° C.
- extractionThe solution was extracted with ethyl acetate (2000 ml)
- dry with materialThe organic layer was dried over sodium sulfate and vacuum
- distillationdistilled
- customto obtain a residue
- customto obtain a solid
- filtrationThe solid was filtered
- washwashed with heptane
- customdried at 50-55° C. under vacuum
Quellen und Nachweise
- ORD-Eintrag
- ord-2ee46eaf334f4abbaa1324e3273770c0
- Quelldatensatz
- uspto-grants-2014_05
- Patentnummer
- US08735589B2
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