Reaktionsgleichung
N1CCNCCNCC1.[C:10]1(C)[CH:15]=CC(S(Cl)(=O)=O)=C[CH:11]=1.[C:21]1([CH3:49])[CH:26]=[CH:25][C:24]([S:27]([N:30]2[CH2:38][CH2:37][NH:36][CH2:35][CH2:34][N:33]([S:39]([C:42]3[CH:47]=[CH:46][C:45]([CH3:48])=[CH:44][CH:43]=3)(=[O:41])=[O:40])[CH2:32][CH2:31]2)(=[O:29])=[O:28])=[CH:23][CH:22]=1.ICCCI.C(=O)([O-])[O-].[K+].[K+]>C(#N)C>[C:21]1([CH3:49])[CH:26]=[CH:25][C:24]([S:27]([N:30]2[CH2:38][CH2:37][NH:36][CH2:35][CH2:34][N:33]([S:39]([C:42]3[CH:47]=[CH:46][C:45]([CH3:48])=[CH:44][CH:43]=3)(=[O:40])=[O:41])[CH2:32][CH2:31]2)(=[O:29])=[O:28])=[CH:23][CH:22]=1.[CH3:11][CH2:10][CH3:15].[C:21]1([CH3:49])[CH:26]=[CH:25][C:24]([S:27]([N:30]2[CH2:38][CH2:37][NH:36][CH2:35][CH2:34][N:33]([S:39]([C:42]3[CH:47]=[CH:46][C:45]([CH3:48])=[CH:44][CH:43]=3)(=[O:40])=[O:41])[CH2:32][CH2:31]2)(=[O:29])=[O:28])=[CH:23][CH:22]=1Komponenten
8
Edukt 5
Produkt 2
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
N,N′-bis(p-Toluenesulfonyl)-1,4,7-triazacyclononane (1.1.20) was prepared by reacting (1.1.3) with two equivalents of p-toluenesulfonyl chloride. Two equivalents of N,N′-bis(p-toluenesulfonyl)-1,4,7-triazacyclononane (1.1.20) hydrobromide were reacted with one equivalent of 1,3-diiodopropane in acetonitrile with excess potassium carbonate. 1,3-bis[N,N′-bis(p-Toluenesulfonyl)-1,4,7-triazacyclononane propane (1.1.21) was isolated and purified by chromatography. The p-toluene-sulfonyl groups were removed using sulfuric acid and HBr to yield the title compound (1.1.19). 1.1.22 1,4,7,10-Tetraazabicyclo[5.5.2]tetradecane
Quellen und Nachweise
- ORD-Eintrag
- ord-40ea47cb16174880a641f1495dd0ae66
- Quelldatensatz
- uspto-grants-2005_04
- Patentnummer
- US06881732B2
Verknüpfte Notizen
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