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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 5852생성일: 2026년 10월 24일

3-(4-(2-Chlorophenyl)piperazin-1-yl)propan-1-ol → 4-(2-Chlorophenyl)-1-[3-(3,4-ethylenedioxyphenylcarbamoyloxy)propyl]piperazine, hydrochloride

https://huagongshe.com/ko/reaction/5852

반응식

참여 물질

역할이름HCID투입량
반응물3-(4-(2-Chlorophenyl)piperazin-1-yl)propan-1-olHCID 243288—
반응물6-Isocyanato-2,3-dihydro-1,4-benzodioxineHCID 2776172—
용매TolueneHCID 1140—
생성물4-(2-Chlorophenyl)-1-[3-(3,4-ethylenedioxyphenylcarbamoyloxy)propyl]piperazine, hydrochlorideHCID 13171816370.5%

반응 단계

A mixture of 3,4-ethylenedioxyphenylisocyanate (2.0 mmol) (produced as in Example 16) and 3-[4-(2-chlorophenyl)-1piperazinyl]propanol (500 mg; 2.0 mmol) in toluene (10 ml) was refluxed for 16 h. The reaction mixture was then concentrated and submitted to flash chromatography on silica gel 60 eluting with toluene graduated to toluene/ethyl acetate (1:5). The product was taken up in ethyl acetate which was treated with hydrogen chloride in ether. Recrystallization from methanol/ether afforded 330 mg of the title compound. M.p. 205°-206° C. MS (70 eV): m/z 431 (14%, M+), 209 (100), 177 (70), 121 (44), 93 (38), 70 (56).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05246935
출처 데이터셋uspto-grants-1993_09
ORD IDord-a42846c208cf4c61a676ead8d617e1cf
출처 메모uspto-grants-1993_09