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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 28523생성일: 2026년 10월 23일

Trifluoroacetic acid → (r)-1-Chloro-3-(4-methylsulfonyl-1-piperazinyl)-2-propanol

https://huagongshe.com/ko/reaction/28523

반응식

참여 물질

역할이름HCID투입량
반응물Trifluoroacetic acidHCID 6422—
반응물DiisopropylethylamineHCID 81531—
반응물(-)-EpichlorohydrinHCID 2734062—
반응물1-PiperazinesulfonamideHCID 11252198—
용매EthanolHCID 702—
생성물(r)-1-Chloro-3-(4-methylsulfonyl-1-piperazinyl)-2-propanolHCID 67338305—

반응 단계

(R)-Epichlorohydrin (3.10 mL, 39.5 mmol) was added to a stirred solution of piperazine sulfonamide.TFA (10.0 g, 35.9 mmol) and diisopropylethylamine (6.26 mL, 35.9 mmol) in ethanol (150 mL) at room temperature. The reaction mixture was stirred for 18 h and a further amount of (R)-epichlorohydrin was added (0.28 mL, 3.6 mmol) and stirred for an additional 3 h. The reaction mixture was concentrated in vacuo and the white solid was suspended in ethanol (150 mL) and stirred for 2 days. The solid was collected by filtration and washed with cold ethanol to afford the title compound (5.69 g) as a white solid which was used without further purification. (m/z): [M+H]+ calcd for C8H17ClN2O3S, 257.07; found 257.2. 1H NMR (DMSO-d6): δ (ppm) 2.37 (dd, 1H), 2.45 (dd, 1H), 2.50-2.58 (m, 4H), 2.86 (s, 3H), 3.09 (m, 4H), 3.55 (dd, 1H), 3.65 (dd, 1H), 3.84 (m, 1H), 5.09 (d, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07419989B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-5f818f97cc914cd680abbe7f915bbd03
출처 메모uspto-grants-2008_09