Sodium Carbonate → 3,3-Dimethyl-1-{2-[4-(7-fluoroindol-3-yl)-1,2,5,6-tetrahydro-1-pyridyl]-1-ethyl}-1,3-dihydro-2H-indol-2-one
Reaktionsgleichung
[F:1][C:2]1[CH:3]=[CH:4][CH:5]=[C:6]2[C:10]=1[NH:9][CH:8]=[C:7]2[C:11]1[CH2:16][CH2:15][NH:14][CH2:13][CH:12]=1.[CH3:17][C:18]1([CH3:35])[C:26]2[C:21](=[CH:22][CH:23]=[CH:24][CH:25]=2)[N:20]([CH2:27][CH2:28]OS(C)(=O)=O)[C:19]1=[O:34].C(=O)([O-])[O-].[Na+].[Na+]>O>[CH3:35][C:18]1([CH3:17])[C:26]2[C:21](=[CH:22][CH:23]=[CH:24][CH:25]=2)[N:20]([CH2:27][CH2:28][N:14]2[CH2:15][CH2:16][C:11]([C:7]3[C:6]4[C:10](=[C:2]([F:1])[CH:3]=[CH:4][CH:5]=4)[NH:9][CH:8]=3)=[CH:12][CH2:13]2)[C:19]1=[O:34]Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
4-(7-Fluoroindol-3-yl)-1,2,5,6-tetrahydropyridine (2.0 g, 9.26 mmols), 3,3-dimethyl-1-(2-methanesulfonyloxy-1-ethyl)-1,3-dihydro-2H-indol-2-one (2.623 g, 9.26 mmols), sodium carbonate (2.947 g,27.8 mmols),water (20 mls) combined and heated to 90 deg C. for 3 hours. Extracted into ethyl acetate (2×50 ml). Dried (MgSO4),filtered and concentrated in vacuo. The resultant solid was recrystallised from ethyl acetate and then converted to the hydrochloride salt (0.85 g).m.p 235-236 deg. C.
Aufarbeitung
- temperatureheated to 90 deg C
- extractionExtracted into ethyl acetate (2×50 ml)
- concentrationDried (MgSO4),filtered and concentrated in vacuo
- customThe resultant solid was recrystallised from ethyl acetate
- customconverted to the hydrochloride salt (0.85 g).m.p 235-236 deg. C
Quellen und Nachweise
- ORD-Eintrag
- ord-79d85607ce6e4207bc0d17bcd9c36a07
- Quelldatensatz
- uspto-grants-2000_12
- Patentnummer
- US06166040
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