Dimethyl Sulfoxide → (S)-10-[3-(3-Methoxy-propyl)-piperazin-1-yl]-4H-3-thia-4,9-diaza-benzo[f]azulene
Reaktionsgleichung
[CH:1]1[C:10]2[C:9]([NH2:11])=[N:8][C:7]3[CH:12]=[CH:13][CH:14]=[CH:15][C:6]=3[NH:5][C:4]=2[S:3][CH:2]=1.[CH3:16][O:17][CH2:18][CH2:19][CH2:20][C@H:21]1[CH2:26]N[CH2:24][CH2:23][NH:22]1.CS(C)=O.C1(C)C=CC=CC=1>C(OCC)(=O)C>[CH3:16][O:17][CH2:18][CH2:19][CH2:20][C@@H:21]1[NH:22][CH2:23][CH2:24][N:11]([C:9]2[C:10]3[CH:1]=[CH:2][S:3][C:4]=3[NH:5][C:6]3[CH:15]=[CH:14][CH:13]=[CH:12][C:7]=3[N:8]=2)[CH2:26]1Komponenten
6
Edukt 4
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 105 °C
Versuchsvorschrift
Combine 4H-3-thia-4,9-diaza-benzo[f]azulen-10-ylamine (1.10 g, 5.11 mmol), (S)-2-(3-methoxy-propyl)-piperazine (1.62 g, 10.22 mmol), DMSO (4.0 ml), and toluene (16.0 ml). Stir and heat the mixture at 105° C. After 45 hours, cool the mixture to ambient temperature. Dilute the mixture with ethyl acetate and wash the organic layer with 0.1N NaOH and brine. Dry (sodium sulfate) and concentrate the organic layer to residue. Purify the residue on silica gel using a gradient of dichloromethane to dichloromethane/methanol (85:15) to give 296.0 mg (16%) of the title compound: mass spectrum (ion spray): m/z=357.2 (M+1).
Aufarbeitung
- temperaturecool the mixture to ambient temperature
- washwash the organic layer with 0.1N NaOH and brine
- dry with materialDry (sodium sulfate)
- concentrationconcentrate the organic layer to residue
- customPurify the residue on silica gel using a gradient of dichloromethane to dichloromethane/methanol (85:15)
Quellen und Nachweise
- ORD-Eintrag
- ord-3dee97c3d13b4db4b517d125a027bbf5
- Quelldatensatz
- uspto-grants-2008_06
- Patentnummer
- US07384934B2
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