Methyl 4-methylaminobenzoate → Methyl 4-{N-[1-(S)-(3-chlorophenyl)-2-(3-(S)-methoxymethoxypyrrolidin-1-yl)-ethyl]-N-methylamino}benzoate
反応式
ClC1C=C([C@@H](N2CC[C@H](OCOC)C2)CO)C=CC=1.[Cl:20][C:21]1[CH:22]=[C:23]([C@H:27](O)[CH2:28][N:29]2[CH2:33][CH2:32][C@H:31]([O:34][CH2:35][O:36][CH3:37])[CH2:30]2)[CH:24]=[CH:25][CH:26]=1.[CH3:39][NH:40][C:41]1[CH:50]=[CH:49][C:44]([C:45]([O:47][CH3:48])=[O:46])=[CH:43][CH:42]=1>>[Cl:20][C:21]1[CH:22]=[C:23]([C@H:27]([N:40]([C:41]2[CH:50]=[CH:49][C:44]([C:45]([O:47][CH3:48])=[O:46])=[CH:43][CH:42]=2)[CH3:39])[CH2:28][N:29]2[CH2:33][CH2:32][C@H:31]([O:34][CH2:35][O:36][CH3:37])[CH2:30]2)[CH:24]=[CH:25][CH:26]=1参加物
4
反応物 3
生成物 1
実験手順
This was prepared from the mixture of 2-(R)-(3-chlorophenyl)-2-(3-(S)-methoxymethoxypyrrolidin-1-yl)ethanol and 1-(S)-(3-chlorophenyl)-2-(3-(S)-methoxymethoxypyrrolidin-1-yl)ethanol and methyl 4-methylaminobenzoate in 66% yield according to a procedure similar to that described in Example 1 (i).