反応式
O[C@@H]1CC[C@H]([N:8]2[C:16](=O)[C:15]3[C:10](=[CH:11][CH:12]=[CH:13]C=3)C2=O)CC1.CC1C=C2C(C=NN2)=CC=1O.[CH3:30][C:31]1[C:39]([OH:40])=[CH:38][CH:37]=[C:36]2[C:32]=1[CH:33]=[N:34][NH:35]2>>[NH:8]1[CH:13]=[CH:12][CH:11]=[C:10]([O:40][C:39]2[C:31]([CH3:30])=[C:32]3[C:36](=[CH:37][CH:38]=2)[NH:35][N:34]=[CH:33]3)[CH:15]=[CH:16]1参加物
4
実験手順
The following compound of Example 408 was synthesized by carrying out reaction according to the method described in Example 385, except for using the cis-2-(4-hydroxycyclohexyl)-1H-isoindole-1,3(2H)-dione obtained in Example 323, (c) and the 4-methyl-1H-indazol-5-ol obtained in Example 402, as starting materials.
後処理
- customreaction
出典と根拠
- ORDレコード
- ord-9ab61364c48340749421189c808884a2
- 出典データセット
- uspto-grants-2007_04
- 特許番号
- US07199147B2
関連ノート
読み込み中…