Hydrochloric Acid → 2-(3-cyanophenylamino)-2-(2-fluorophenyl)-N-[3-methyl-4-(2-oxopiperidin-1-yl)phenyl]acetamide, hydrochloride
Reaktionsgleichung
[ClH:1].[C:2]([C:4]1[CH:5]=[C:6]([NH:10][CH:11]([C:29]2[CH:34]=[CH:33][CH:32]=[CH:31][C:30]=2[F:35])[C:12]([NH:14][C:15]2[CH:20]=[CH:19][C:18]([N:21]3[CH2:26][CH2:25][CH2:24][CH2:23][C:22]3=[O:27])=[C:17]([CH3:28])[CH:16]=2)=[O:13])[CH:7]=[CH:8][CH:9]=1)#[N:3]>CC(O)C>[ClH:1].[C:2]([C:4]1[CH:5]=[C:6]([NH:10][CH:11]([C:29]2[CH:34]=[CH:33][CH:32]=[CH:31][C:30]=2[F:35])[C:12]([NH:14][C:15]2[CH:20]=[CH:19][C:18]([N:21]3[CH2:26][CH2:25][CH2:24][CH2:23][C:22]3=[O:27])=[C:17]([CH3:28])[CH:16]=2)=[O:13])[CH:7]=[CH:8][CH:9]=1)#[N:3]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
1.87 ml of 0.1N HCl in 2-propanol are added to 86 mg (0.187 mmol) of 2-(3-cyanophenylamino)-2-(2-fluorophenyl)-N-[3-methyl-4-(2-oxopiperidin-1-yl)phenyl]acetamide, and the mixture is left to stand at room temperature for 2 hours. The reaction mixture is evaporated and subsequently lyophilised, giving 2-(3-cyanophenylamino)-2-(2-fluorophenyl)-N-[3-methyl-4-(2-oxopiperidin-1-yl)phenyl]acetamide, hydrochloride, as a colourless solid; ESI 460.