Reaktionsgleichung
CS(O)(=O)=O.[Cl:6][C:7]1[C:15]2[N:14]([CH2:16][CH2:17][CH2:18]O)[C:13](=[O:20])[NH:12][C:11]=2[CH:10]=[CH:9][CH:8]=1.[C:21]1([N:27]2[C:31]3([CH2:36][CH2:35][NH:34][CH2:33][CH2:32]3)[C:30](=[O:37])[NH:29][CH2:28]2)[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1.C(=O)([O-])[O-].[Na+].[Na+].CC(C)CC(=O)C>O>[Cl:6][C:7]1[C:15]2[N:14]([CH2:16][CH2:17][CH2:18][N:34]3[CH2:33][CH2:32][C:31]4([N:27]([C:21]5[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=5)[CH2:28][NH:29][C:30]4=[O:37])[CH2:36][CH2:35]3)[C:13](=[O:20])[NH:12][C:11]=2[CH:10]=[CH:9][CH:8]=1Komponenten
6
Edukt 4
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A mixture of 4.2 parts of 4-chloro-1,3-dihydro-3-(3-hydroxypropyl)-2H-benzimidazol-2-one methane sulfonate, 2.5 parts of 1-phenyl-1,3,8-triazaspiro[4,5]decan-4-one, 10 parts of sodium carbonate and 80 parts of 4-methyl-2-pentanone is stirred and refluxed overnight. The reaction mixture is cooled and water is added. The precipitated product is filtered off and crystallized twice from a mixture of N,N-dimethylformamide and water, yielding 0.8 parts (17%) of 8-[3-(7-chloro-1,3-dihydro-2-oxo-2H-benzimidazol-1-yl)propyl]-1-phenyl-1,3,8-triazaspiro[4,5]decan-4-one; mp. 258.4° C.
Aufarbeitung
- temperaturerefluxed overnight
- temperatureThe reaction mixture is cooled
- filtrationThe precipitated product is filtered off
- customcrystallized twice from a mixture of N,N-dimethylformamide and water
Quellen und Nachweise
- ORD-Eintrag
- ord-de8043b3f6a142a0be495480f4905990
- Quelldatensatz
- uspto-grants-1979_11
- Patentnummer
- US04175129
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