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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 5857생성일: 2026년 10월 24일

3,4,5-Trimethoxyphenyl isothiocyanate → 4-(3-Chlorophenyl)-1-(3-[3,4,5-trimethoxyphenyl(thiocarbamoyl)oxy]propyl)piperazine, hydrochloride

https://huagongshe.com/ko/reaction/5857

반응식

참여 물질

역할이름HCID투입량
반응물3,4,5-Trimethoxyphenyl isothiocyanateHCID 118900—
반응물3-(4-(3-Chlorophenyl)piperazin-1-yl)propan-1-olHCID 257407—
용매TolueneHCID 1140—
생성물4-(3-Chlorophenyl)-1-(3-[3,4,5-trimethoxyphenyl(thiocarbamoyl)oxy]propyl)piperazine, hydrochlorideHCID 13171816538.7%

반응 단계

A mixture of 3,4,5-trimethoxyphenylisothiocyanate (2.0 mmol) (produced as in Example 22) and 3-[4-(3-chlorophenyl) -1-piperazinyl]propanol (510 mg; 2.0 mmol) in toluene (40 ml) was refluxed for 16 h. The solvent was evaporated and the residue resuspended in ethyl acetate, filtered and evaporated to dryness. The residue was submitted to flash chromatography on silica gel 60 eluting with toluene/ethyl acetate (1:1). The product was taken up in ethanol, which was treated with hydrogen chloride in ether to give 200 mg of the title compound. M.p. 175°-176° C. MS (70 eV): m/z 479 (M+, 0.5%), 254 (49), 225 (88), 209 (100), 182 (34).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05246935
출처 데이터셋uspto-grants-1993_09
ORD IDord-32f0e1a47d884b0fa22a2aeb54b8e2e5
출처 메모uspto-grants-1993_09