反応式
[NH2:1][C:2]1[S:3][CH:4]=[CH:5][N:6]=1.[CH:7]1([N+:13]#[C-:14])[CH2:12][CH2:11][CH2:10][CH2:9][CH2:8]1.[CH3:15][C:16]1[CH:23]=[CH:22][C:21]([CH3:24])=[CH:20][C:17]=1[CH:18]=O>Cl(O)(=O)(=O)=O>[CH:7]1([NH:13][C:14]2[N:6]3[C:2]([S:3][CH:4]=[CH:5]3)=[N:1][C:18]=2[C:17]2[CH:20]=[C:21]([CH3:24])[CH:22]=[CH:23][C:16]=2[CH3:15])[CH2:12][CH2:11][CH2:10][CH2:9][CH2:8]1参加物
5
実験手順
Compound 51 was prepared in accordance with the general synthesis instructions from 1.0 ml (0.1 mmol) 2-amino thiazole solution (0.1 M, MC), 0.575 ml (0.115 mmol) cyclohexylisonitrile solution (0.2 M, MC), 0.500 ml (0.15 mmol) 2,5-dimethylbenzaldehyde solution (0.3 M, MC) and 10 μl perchloric acid (w=20%) in a substance library.
出典と根拠
- ORDレコード
- ord-fec350a9ff16484ea6572d95db4d29ec
- 出典データセット
- uspto-grants-2003_12
- 特許番号
- US06657064B2
関連ノート
読み込み中…