反応式
[C:1]([C:5]1[CH:6]=[C:7]([CH:10]=[C:11]([C:14]([CH3:17])([CH3:16])[CH3:15])[C:12]=1[OH:13])[CH:8]=O)([CH3:4])([CH3:3])[CH3:2].[CH3:18][N:19]([CH3:27])[N:20]1[C:24](=[O:25])[CH2:23][S:22][C:21]1=[S:26]>>[CH3:4][C:1]([C:5]1[CH:6]=[C:7]([CH:8]=[C:23]2[S:22][C:21](=[S:26])[N:20]([N:19]([CH3:27])[CH3:18])[C:24]2=[O:25])[CH:10]=[C:11]([C:14]([CH3:17])([CH3:16])[CH3:15])[C:12]=1[OH:13])([CH3:2])[CH3:3]参加物
3
実験手順
The title compound was prepared in 65% yield from 3,5-di-tert-butyl-4-hydroxybenzaldehyde and N-dimethylaminorhodanine following the procedure of Example 1.
出典と根拠
- ORDレコード
- ord-3fc53c58da5541b7be879e3d056e8312
- 出典データセット
- uspto-grants-1995_02
- 特許番号
- US05387690
関連ノート
読み込み中…