反応式
[F:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]([O:10][C:11]2[CH:16]=[CH:15][NH:14][C:13](=[O:17])[CH:12]=2)[CH3:9])=[CH:4][CH:3]=1.C(OC1C=CN(C2C=CC([O:38][CH2:39][CH2:40][N:41]3[CH2:46][CH2:45][CH2:44][CH2:43]C3)=CN=2)C(=O)C=1)C1C=CC=CC=1.C(O)[C:49]1[CH:54]=[CH:53][CH:52]=[CH:51][CH:50]=1.FC1C=CC(C(O)C)=CC=1.C(OC1C=CNC(=O)C=1)C1C=CC=CC=1>>[F:1][C:2]1[CH:3]=[CH:4][C:5]([CH:8]([O:10][C:11]2[CH:16]=[CH:15][N:14]([C:52]3[CH:51]=[CH:50][C:49]([O:38][CH2:39][CH2:40][N:41]4[CH2:46][CH2:45][CH2:44][CH2:43]4)=[CH:54][CH:53]=3)[C:13](=[O:17])[CH:12]=2)[CH3:9])=[CH:6][CH:7]=1参加物
6
反応物 5
生成物 1
実験手順
Example 12 was repeated except that 4-[1-(4-fluorophenyl)ethoxy]-1H-pyridin-2-one as obtained by repeating Steps (1) and (2) of Example 1 in which benzyl alcohol was replaced with 1-(4-fluorophenyl)ethanol, was used in place of 4-benzyloxy-1H-pyridin-2-one, to provide the title compound.
後処理
- customas obtained
出典と根拠
- ORDレコード
- ord-f4d25164b2b74b7ebebb66f4dc242b34
- 出典データセット
- uspto-grants-2010_06
- 特許番号
- US07732456B2
関連ノート
読み込み中…