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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | 1-(4-Methylbenzenesulfonyl)aziridine | HCID 561274 | — |
| 반응물 | 2-(4-Chloro-benzenesulfonylmethyl)-1,3,4-trifluoro-benzene | HCID 58950334 | — |
| 반응물 | Butyllithium | HCID 178418339 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 용매 | Thf tmeda | HCID 86588997 | — |
| 생성물 | [3-(4-Chloro-benzenesulfonyl)-3-(2,3,6-trifluoro-phenyl)-propyl]-4-methyl-benzenesulfonamide | HCID 131729296 | 54.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08067621B2 |
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| 출처 데이터셋 | uspto-grants-2011_11 |
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| ORD ID | ord-631d4db9398848089264d4ee1eeb1764 |
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| 출처 메모 | uspto-grants-2011_11 |
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