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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 564342생성일: 2026년 10월 24일

1-(4-Methylbenzenesulfonyl)aziridine → [3-(4-Chloro-benzenesulfonyl)-3-(2,3,6-trifluoro-phenyl)-propyl]-4-methyl-benzenesulfonamide

https://huagongshe.com/ko/reaction/564342

반응식

참여 물질

역할이름HCID투입량
반응물1-(4-Methylbenzenesulfonyl)aziridineHCID 561274—
반응물2-(4-Chloro-benzenesulfonylmethyl)-1,3,4-trifluoro-benzeneHCID 58950334—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
용매Thf tmedaHCID 86588997—
생성물[3-(4-Chloro-benzenesulfonyl)-3-(2,3,6-trifluoro-phenyl)-propyl]-4-methyl-benzenesulfonamideHCID 13172929654.1%

반응 단계

A solution of 2-(4-chloro-benzenesulfonylmethyl)-1,3,4-trifluoro-benzene (5.6 g, 17.5 mmol) in THF/TMEDA (5:1, 180 mL) at −78° C. was treated with n-BuLi (12 mL, 17.5 mmol, 1.5 M in hexanes). After 15 min, a solution of N-p-toluenesulfonyl aziridine (3.5 g, 17.5 mmol, prepared as described in Eur. J. Org. Chem. 2002, 3004) in THF (10 mL) was added, and the reaction mixture warmed slowly to ambient temperature. After 4 h, the reaction mixture was quenched with 1N HCl and extracted with EtOAc (2×). The combined organic extracts were washed with saturated aqueous NaHCO3, brine, dried over MgSO4 and concentrated in vacuo. Flash chromatography (25→50% EtOAc/Hex) provided the title compound (4.9 g, 54%): 1H NMR (CDCl3 400 MHz) δ 7.64 (d, J=8.1 Hz, 2H), 7.57 (d, J=8.1 Hz, 2H), 7.43 (d, J=8.1 Hz, 2H), 7.28 (d, J=8.1 Hz, 2H), 7.14 (m, 1H), 6.75 (m, 1H), 4.81 (m, 1H), 3.17 (ddd, J=7.1, 7.1, 5.6 Hz, 1H), 2.96 (m, 1H), 2.64 (m, 1H), 2.47 (m, 1H), 2.41 (s, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08067621B2
출처 데이터셋uspto-grants-2011_11
ORD IDord-631d4db9398848089264d4ee1eeb1764
출처 메모uspto-grants-2011_11