[CH3:1][N:2]([CH2:4][C:5]1[O:25][C:8]2[CH2:9][N:10]([CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][C:19]3[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=3)[CH2:11][CH2:12][C:7]=2[CH:6]=1)[CH3:3].[ClH:26]>CO>[ClH:26].[ClH:26].[CH3:1][N:2]([CH2:4][C:5]1[O:25][C:8]2[CH2:9][N:10]([CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][C:19]3[CH:20]=[CH:21][CH:22]=[CH:23][CH:24]=3)[CH2:11][CH2:12][C:7]=2[CH:6]=1)[CH3:3]N,N-Dimethyl-[6-(6-phenylhexyl)-4,5,6,7-tetrahydrofuro[2,3-c]pyridin-2-ylmethyl]amine 0.088 g was dissolved in 2 ml of methanol; hydrogen chloride in methanol was added in excess, followed by stirring. This mixture was concentrated to yield the desired product.
Loading…