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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 70060생성일: 2026년 10월 23일

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

https://huagongshe.com/ko/reaction/70060

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 번호US08822513B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-f613d3706ed846c89d6ff52f90c5d1df
출처 메모uspto-grants-2014_09