4-Fluoroaniline → 2,5-Bis(4-bromophenyl)-1-(4-tert-butylphenyl)pyrrolidine
反応式
CS(O[CH:6]([C:22]1[CH:27]=[CH:26][C:25]([Br:28])=[CH:24][CH:23]=1)[CH2:7][CH2:8][CH:9](OS(C)(=O)=O)[C:10]1[CH:15]=[CH:14][C:13]([Br:16])=[CH:12][CH:11]=1)(=O)=O.F[C:30]1[CH:36]=[CH:35][C:33]([NH2:34])=[CH:32][CH:31]=1>>[Br:16][C:13]1[CH:14]=[CH:15][C:10]([CH:9]2[CH2:8][CH2:7][CH:6]([C:22]3[CH:27]=[CH:26][C:25]([Br:28])=[CH:24][CH:23]=3)[N:34]2[C:33]2[CH:35]=[CH:36][C:30]([C:10]([CH3:15])([CH3:11])[CH3:9])=[CH:31][CH:32]=2)=[CH:11][CH:12]=1参加物
3
実験手順
The product from Example 42B (5.2 g, 9.35 mmol) was subjected to the conditions described in Example 39D, substituting 4-tert-butylaniline (11.91 mL, 74.8 mmol) for 4-fluoroaniline to provide the title product (3.89 g, 81%) as a mixture of isomers.
出典と根拠
- ORDレコード
- ord-36184d768c404fdc8e81c65f7f336084
- 出典データセット
- uspto-grants-2015_04