3-{2-(3-Chloro-5-fluorophenyl)-5-[(4-oxoimidazolidin-1-yl)carbonyl]thiophen-3-yl}benzenecarbonitrile → 5-{2-(3-Chloro-5-fluorophenyl)-5-[(4-oxoimidazolidin-1-yl)carbonyl]thiophen-3-yl}-2-fluorobenzenecarbonitrile
反応式
[Cl:1][C:2]1[CH:3]=[C:4]([C:9]2[S:10][C:11]([C:22]([N:24]3[CH2:28][C:27](=[O:29])[NH:26][CH2:25]3)=[O:23])=[CH:12][C:13]=2[C:14]2[CH:15]=[C:16]([C:20]#[N:21])[CH:17]=[CH:18][CH:19]=2)[CH:5]=[C:6]([F:8])[CH:7]=1.ClC1C=C(C2SC(C(O)=O)=CC=2C2C=CC(F)=C(C#N)C=2)C=C([F:37])C=1>>[Cl:1][C:2]1[CH:3]=[C:4]([C:9]2[S:10][C:11]([C:22]([N:24]3[CH2:28][C:27](=[O:29])[NH:26][CH2:25]3)=[O:23])=[CH:12][C:13]=2[C:14]2[CH:19]=[CH:18][C:17]([F:37])=[C:16]([C:20]#[N:21])[CH:15]=2)[CH:5]=[C:6]([F:8])[CH:7]=1参加物
3
反応物 2
生成物 1
実験手順
The preparation of the title compound takes place in analogy to the synthesis of the compound from Example 1 starting with 82.3 mg (0.22 mmol) of the compound from Example 22A. 35.0 mg (35% of theory) of the title compound are obtained.
出典と根拠
- ORDレコード
- ord-0acb4ce2baad4702920540d8e211d802
- 出典データセット
- uspto-grants-2013_10
- 特許番号
- US08546438B2
反応ノート
読み込み中…