m-Chloroperbenzoic acid → HCID 10401503, Verbindung
Reaktionsgleichung
ClC1C=CC=C(C(OO)=[O:9])C=1.[C:12]([C:14]1[C:15]([N:26]2[CH2:31][CH2:30][O:29][CH2:28][CH2:27]2)=[N:16][CH:17]=[C:18]([C:20]2[CH:25]=[CH:24][N:23]=[CH:22][CH:21]=2)[CH:19]=1)#[N:13]>C(Cl)(Cl)Cl>[C:12]([C:14]1[C:15]([N:26]2[CH2:31][CH2:30][O:29][CH2:28][CH2:27]2)=[N:16][CH:17]=[C:18]([C:20]2[CH:21]=[CH:22][N+:23]([O-:9])=[CH:24][CH:25]=2)[CH:19]=1)#[N:13]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
1.1 g M-chloroperbenzoic acid is added at room temperature with stirring to a solution of 1.3 g 3-cyano-2-morpholino-5-(pyrid-4-yl)-pyridine in 20 ml chloroform. The reaction mixture is stirred for 48 hours at room temperature. Subsequently it is extracted with a bicarbonate solution and the chloroform phase is evaporated under vacuum. The residue is treated with water, filtered off with suction, dried at 110° C., and crystallized from a mixture of isopropanol and ethanol. Yield: 1.0 g (73% of the theoretical yield), with a melting point of 233° C.-235° C.