戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 256822作成日:2026年10月27日

Methanol → 2-Imino-3-{2-[4-(2-methylphenyl)-1-piperazinyl]ethyl}-6-trifluoromethoxybenzothiazoline

https://huagongshe.com/reaction/256822

反応式

関与物質

役割名称HCID仕込み量
反応物MethanolHCID 887—
反応物Potassium CarbonateHCID 11430—
反応物2-MeppHCID 91965—
反応物2-(2-Trifluoroacetylimino-6-trifluoromethoxy-3-benzothiazolinyl)ethyl methanesulphonateHCID 15734864—
溶媒TolueneHCID 1140—
生成物2-Imino-3-{2-[4-(2-methylphenyl)-1-piperazinyl]ethyl}-6-trifluoromethoxybenzothiazolineHCID 1573486731.7%

反応条件

温度20 °C

反応手順

Using the procedure described in Example 1, starting with 2-(2-trifluoroacetylimino-6-trifluoromethoxy-3-benzothiazolinyl)ethyl methanesulphonate (5.88 g) in toluene (200 cc) and 4-(2-methylphenyl)piperazine (6.87 g) and after 2 hours under reflux, the toluene filtrate is evaporated under reduced pressure. To the residue thereby obtained, methanol (100 cc) and a 7% strength aqueous-alcoholic solution (20 cc) of potassium carbonate are added and the mixture is stirred for 2 hours at approximately 20° C. The alcohol is evaporated off under reduced pressure and the residue is purified by chromatography on a silica column with a dichloromethane/ethyl acetate mixture (70:30 by volume) as eluent, and then an ethyl acetate/cyclohexane mixture (50:50 by volume) as eluent. 2-Imino-3-{2-[4-(2-methylphenyl)-1-piperazinyl]ethyl}-6-trifluoromethoxybenzothiazoline (1.8 g), m.p. 135° C., is thereby obtained.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05260297
出典データセットuspto-grants-1993_11
ORD IDord-dc629171cd6642ad9df22a945bf19afc
出典メモuspto-grants-1993_11