反応式
FC1C=C(F)C=CC=1C1C=C(CN2C(=O)C3=CC=CC=C3C2=O)C(=O)N(CC(C)C)N=1.[C:32]([C:35]1[C:36](=[O:53])[N:37]([CH2:49][CH:50]([CH3:52])[CH3:51])[N:38]=[C:39]([C:41]2[CH:46]=[CH:45][C:44]([S:47][CH3:48])=[CH:43][CH:42]=2)[CH:40]=1)(O)=[O:33]>>[OH:33][CH2:32][C:35]1[C:36](=[O:53])[N:37]([CH2:49][CH:50]([CH3:51])[CH3:52])[N:38]=[C:39]([C:41]2[CH:46]=[CH:45][C:44]([S:47][CH3:48])=[CH:43][CH:42]=2)[CH:40]=1参加物
3
実験手順
Following the procedure of Example 1 (8), 4-carboxy-2-isobutyl-6-[4-(methylthio)phenyl]-2H-pyridazin-3-one was reacted to yield the title compound as a yellow oil (yield: 35.3%).
後処理
- customwas reacted
出典と根拠
- ORDレコード
- ord-4890823ff7fb4745a8939acecea10f65
- 出典データセット
- uspto-grants-2006_08
- 特許番号
- US07087606B2
関連ノート
読み込み中…