Hydrochloric Acid → 3-[2,4-Dichloro-6-fluorobenzothiazol-7-yl]-6-trifluoromethyl-2,4(1H,3H)-pyrimidinedione
反応式
[H-].[Na+].[NH2:3][C:4]([C:12]([F:15])([F:14])[F:13])=[CH:5][CH2:6]C(OCC)=O.[Cl:16][C:17]1[S:18][C:19]2[C:25]([N:26]=[C:27]=[O:28])=[C:24]([F:29])[CH:23]=[C:22]([Cl:30])[C:20]=2[N:21]=1.Cl.CN(C)C=[O:35]>O1CCCC1>[Cl:16][C:17]1[S:18][C:19]2[C:25]([N:26]3[C:6](=[O:35])[CH:5]=[C:4]([C:12]([F:13])([F:14])[F:15])[NH:3][C:27]3=[O:28])=[C:24]([F:29])[CH:23]=[C:22]([Cl:30])[C:20]=2[N:21]=1参加物
反応物 5
生成物 1
試薬・触媒・溶媒 1
反応条件
- 温度
- -30 °C
実験手順
1.6 g of sodium hydride (97% strength) in 200 ml of absolute dimethylformamide were initially taken. 11.0 g of ethyl 3-amino-4,4,4-trifluorobut-2-enecarboxylate were then added dropwise at from 0° to 5° C. Stirring was carried out for one hour at this temperature, after which the mixture was cooled to -30° C. and 16.2 g of 2,4-dichloro-6-fluoro-7-isocyanatobenzothiazole in 50 ml of absolute tetrahydrofuran were then added dropwise. The mixture was stirred for one hour at this temperature and then slowly warmed up to room temperature. Thereafter, ice water was added and the pH was brought to 3-4 with dilute hydrochloric acid, after which the product was extracted with ethyl acetate. The ester solution was dried and then evaporated down.
後処理
- stirringThe mixture was stirred for one hour at this temperature
- temperatureslowly warmed up to room temperature
- extractionafter which the product was extracted with ethyl acetate
- dry with materialThe ester solution was dried
- customevaporated down
出典と根拠
- ORDレコード
- ord-a5d3fbc8e7f243e58666a6a5d172497f
- 出典データセット
- uspto-grants-1999_03
- 特許番号
- US05888940
反応ノート
読み込み中…