反応式
[NH2:1][C:2]1[S:6][N:5]=[C:4]([CH2:7][CH3:8])[C:3]=1[C:9]#[N:10].[Cl-].[Cl:12][C:13](Cl)=[N+:14]([CH3:16])[CH3:15]>ClCCl>[C:9]([C:3]1[C:4]([CH2:7][CH3:8])=[N:5][S:6][C:2]=1[N:1]=[C:13]([Cl:12])[N:14]([CH3:16])[CH3:15])#[N:10]参加物
4
実験手順
In the manner of Example VI, 7.6 g of 5-amino-4 -cyano-3-ethylisothiazole and 8.1 g of N-(dichloromethylene) -N,N-dimethylammonium chloride were allowed to react in 100 ml of dichloromethane. The volatile materials were evaporated under reduced pressure. The residue was recrystallized twice from cyclohexane to give 2.0 g of N'-(4-cyano-3-ethyl-5-isothiazolyl)-N,N-dimethylchloroformamidine, mp 95°-97°. The nmr spectrum was consistent with the assigned structure.
後処理
- customThe volatile materials were evaporated under reduced pressure
- customThe residue was recrystallized twice from cyclohexane
出典と根拠
- ORDレコード
- ord-a72d35e7189c43719183e11077ed6902
- 出典データセット
- uspto-grants-1977_06
- 特許番号
- US04032322
関連ノート
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