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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 256822생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/256822

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참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물Potassium CarbonateHCID 11430—
반응물2-MeppHCID 91965—
반응물2-(2-Trifluoroacetylimino-6-trifluoromethoxy-3-benzothiazolinyl)ethyl methanesulphonateHCID 15734864—
용매TolueneHCID 1140—
생성물2-Imino-3-{2-[4-(2-methylphenyl)-1-piperazinyl]ethyl}-6-trifluoromethoxybenzothiazolineHCID 1573486731.7%

반응 조건

온도20 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05260297
출처 데이터셋uspto-grants-1993_11
ORD IDord-dc629171cd6642ad9df22a945bf19afc
출처 메모uspto-grants-1993_11