Dimethylformamide → HCID 19936722、化合物
反応式
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]2[S:9][C:8]3=[N:10][C:11]([C:20]4[CH:24]=[C:23]([CH3:25])[S:22][C:21]=4[CH3:26])=[C:12]([CH:13](O)[C:14]([N:16]([CH3:18])[CH3:17])=[O:15])[N:7]3[C:6]=2[CH:27]=1.S(Cl)([Cl:30])=O.CN(C)C=O>ClCCl>[ClH:1].[Cl:30][CH:13]([C:12]1[N:7]2[C:8]([S:9][C:5]3[CH:4]=[CH:3][C:2]([Cl:1])=[CH:27][C:6]=32)=[N:10][C:11]=1[C:20]1[CH:24]=[C:23]([CH3:25])[S:22][C:21]=1[CH3:26])[C:14]([N:16]([CH3:18])[CH3:17])=[O:15]参加物
実験手順
18 g (0.0431 mole) of 6-chloro-α-hydroxy-N,N-dimethyl-2-(2,5-dimethylthien-3-yl)imidazo[2,1-b]benzothiazole-3-acetamide are treated with 31 ml (0.43 mole) of thionyl chloride, 2 ml of N,N-dimethyl formamide and 100 ml of dichloromethane at the reflux temperature for 6 h. The solvent and the excess thionyl chloride are removed under reduced pressure, the residue is taken up in diethyl ether, the solid is washed with diethyl ether and it is dried. 21 g of α,6-dichloro-N,N-dimethyl-2-(2,5-dimethylthien-3-yl)imidazo[2,1-b]benzothiazole-3-acetamide hydrochloride are obtained which are reduced with 21 g (0.136 mole) of Rongalite® in 300 ml of dichloromethane at room temperature for 24 h. The solution is separated after settling has taken place, the solid is washed with dichloromethane, the organic phase is washed with a saturated sodium hydrogen carbonate solution and then with water, it is dried over sodium sulphate and the solvent is evaporated under reduced pressure. An oil is obtained which crystallizes and which is recrystallized from acetonitrile. 14.4 g of yellow needles are finally isolated. Melting point: 202°-203° C.
後処理
- customThe solvent and the excess thionyl chloride are removed under reduced pressure
- washthe solid is washed with diethyl ether and it
- customis dried
出典と根拠
- ORDレコード
- ord-b5cf16699b15485896e46c2aceaeb875
- 出典データセット
- uspto-grants-1995_05
- 特許番号
- US05418248
反応ノート
読み込み中…