反応式
[Cl:1][C:2]1[CH:21]=[CH:20][C:5]([CH2:6][N:7]2[C:15]3[C:10](=[CH:11][CH:12]=[CH:13][CH:14]=3)[C:9]([C:16]([OH:19])(C)[CH3:17])=[N:8]2)=[C:4]([CH3:22])[CH:3]=1.ClC1C=CC(CN2C3C(=CC=CC=3)C(C=O)=N2)=C(C)C=1>>[Cl:1][C:2]1[CH:21]=[CH:20][C:5]([CH2:6][N:7]2[C:15]3[C:10](=[CH:11][CH:12]=[CH:13][CH:14]=3)[C:9]([CH:16]([OH:19])[CH3:17])=[N:8]2)=[C:4]([CH3:22])[CH:3]=1参加物
3
実験手順
The product was obtained using the method described for the preparation of compound 10b, but using as starting material compound 12a (0.4 mol) instead of compound 10a.
後処理
- customThe product was obtained
出典と根拠
- ORDレコード
- ord-b0b8411721cb41eeaee248e4ecef4f21
- 出典データセット
- uspto-grants-2016_02
- 特許番号
- US09255073B2
関連ノート
読み込み中…