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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 63233생성일: 2026년 10월 23일

Pentane → (2-(4-Chlorophenyl)-1-(phenylsulfonyl)-1H-imidazol-4-yl)(3,4,5-trimethoxyphenyl)methanone

https://huagongshe.com/ko/reaction/63233

반응식

참여 물질

역할이름HCID투입량
반응물PentaneHCID 8003—
반응물Benzoyl chloride, 3,4,5-trimethoxy-HCID 78282—
반응물2-(4-Chlorophenyl)-1-(phenylsulfonyl)-1H-imidazoleHCID 49788500—
반응물HCID 178418306HCID 178418306—
용매TetrahydrofuranHCID 8028—
용매Sodium BicarbonateHCID 516892—
생성물(2-(4-Chlorophenyl)-1-(phenylsulfonyl)-1H-imidazol-4-yl)(3,4,5-trimethoxyphenyl)methanoneHCID 4978880236.8%

반응 단계

To a solution of 2-(4-chlorophenyl)-1-(phenylsulfonyl)-1H-imidazole (10f) (6.0 mmol) in anhydrous THF (30 mL) at −78° C. was added 1.7 M tert-butyllithium in pentane (5.3 mL, 9.0 mmol) and stirred for 10 min. 3,4,5-Trimethoxybenzoyl chloride (7.2 mmol) was added at −78° C. and stirred for overnight. The reaction mixture was diluted with 100 mL of saturated NaHCO3 solution (aqueous) and extracted by ethyl acetate (200 mL). The organic layer was dried over magnesium sulfate and concentrated. The residue was purified by flash column chromatography (hexane:ethyl acetate 4:1) to give a white solid. Yield: 36.8%; 1H NMR (500 MHz, CDCl3) δ 8.05 (d, J=7.5 Hz, 2H), 7.77 (t, J=7.5 Hz, 1H), 7.62 (t, J=8.0 Hz, 2H), 7.48 (s, 1H), 7.44 (d, J=9.0 Hz, 2H), 7.39 (d, J=8.5 Hz, 2H), 7.37 (s, 2H). MS (ESI): calculated for C25H21ClN2O6S, 512.1. found 513.1 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09447049B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-e16d5251861942d0865ec6ca7d3f8d39
출처 메모uspto-grants-2016_09