Sodium Hydroxide → N-methyl-N-(3,4-dichlorostyryl)acetamidine
反応式
CNC(=NS([CH:9]=[CH:10][C:11]1[CH:16]=[CH:15][C:14]([Cl:17])=[C:13]([Cl:18])[CH:12]=1)(=O)=O)C.[OH-].[Na+].[CH3:21][N:22](C=CC1C=CC([N+]([O-])=O)=CC=1)[C:23](=[NH:30])[C:24]1C=CC=CC=1>CC(C)=O>[CH3:21][N:22]([CH:9]=[CH:10][C:11]1[CH:16]=[CH:15][C:14]([Cl:17])=[C:13]([Cl:18])[CH:12]=1)[C:23](=[NH:30])[CH3:24]参加物
5
実験手順
Treating N-methyl-N'-(3,4-dichlorostyrylsulfonyl)acetamidine with aqueous sodium hydroxide in acetone according to the procedure of Example 32 (c) provides N-methyl-N-(3,4-dichlorostyryl)acetamidine.
出典と根拠
- ORDレコード
- ord-4a955448088f44508a2c5cf4fd568806
- 出典データセット
- uspto-grants-1980_06
- 特許番号
- US04206142
反応ノート
読み込み中…