Triethylamine → 1,2-Dihydro-3-methyl-1-[6-[(2,2,2-trifluoro)ethanesulfonamido]hexan-1-yl)-1,4,7b-triazacyclopent[cd]inden-2-one
Reaktionsgleichung
[NH2:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][N:8]1[C:16]2[N:11]3[C:12](=[N:17][C:18]([CH3:19])=[C:10]3[C:9]1=[O:20])[CH:13]=[CH:14][CH:15]=2.C(N(CC)CC)C.[F:28][C:29]([F:36])([F:35])[CH2:30][S:31](Cl)(=[O:33])=[O:32]>C(Cl)Cl>[CH3:19][C:18]1[N:17]=[C:12]2[CH:13]=[CH:14][CH:15]=[C:16]3[N:11]2[C:10]=1[C:9](=[O:20])[N:8]3[CH2:7][CH2:6][CH2:5][CH2:4][CH2:3][CH2:2][NH:1][S:31]([CH2:30][C:29]([F:36])([F:35])[F:28])(=[O:33])=[O:32]Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
To a solution of 676 mg (2.48 mmol) of 1-[6-(amino)hexyl]-1,2-dihydro-3-methyl-1,4,7b-triazacyclopent[cd]inden-2-one and 0.52 ml (3.73 mmol) of triethylamine in 30 ml of methylene chloride was added, while stirring under ice-cooling, 0.55 g (3.01 mmol) of 2,2,2-trifluoroethanesulfonylchloride, and the mixture was stirred for 30 minutes at the same temperature range. The reaction mixture was washed with an aqueous solution of sodium hydrogencarbonate, dried over anhydrous magnesium sulfate. The solvent was distilled off, and the residue was purified by column chromatography (eluent: ethyl acetate) to give 802 mg of the desired compound (77.2%, pale brown solid).
Aufarbeitung
- temperaturecooling
- washThe reaction mixture was washed with an aqueous solution of sodium hydrogencarbonate
- dry with materialdried over anhydrous magnesium sulfate
- distillationThe solvent was distilled off
- customthe residue was purified by column chromatography (eluent: ethyl acetate)
Quellen und Nachweise
- ORD-Eintrag
- ord-7576a0e1648a4f019dd692bcea9e7d93
- Quelldatensatz
- uspto-grants-2001_06
- Patentnummer
- US06251905B1
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