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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 52306생성일: 2026년 10월 23일

Bromomethyl 4-methoxyphenyl ketone → 2-(4-chlorophenyl)-4-(4-methoxyphenyl)-1-(4-(methylsulfonyl)phenyl]-4-(4-methoxyphenyl)-1H-imidazole

https://huagongshe.com/ko/reaction/52306

반응식

참여 물질

역할이름HCID투입량
반응물Bromomethyl 4-methoxyphenyl ketoneHCID 4965—
반응물Sodium BicarbonateHCID 516892—
반응물4-chloro-N-[4-(methylsulfonyl)phenyl]benzenecarboximidamideHCID 178504796—
용매IsopropanolHCID 3776—
생성물2-(4-chlorophenyl)-4-(4-methoxyphenyl)-1-(4-(methylsulfonyl)phenyl]-4-(4-methoxyphenyl)-1H-imidazoleHCID 22998078113.4%

반응 단계

To a mixture of 4-chloro-N-[4-(methylsulfonyl)phenyl]benzenecarboximidamide (Example 1, Step 1) (700 mg, 2.24 mmol) and sodium bicarbonate (376 mg, 4.48 mmol) in isopropanol (50 mL), 4-methoxyphenacyl bromide (1.03 g, 4.48 mmol) was added. After heating the reaction mixture at 75°-80° C. for 20 hours, the solvent was removed. The residue was redissolved in methylene chloride and washed with aqueous sodium bicarbonate and water. The organic fractions were combined, dried over sodium sulfate, filtered and concentrated in vacuo. The crude product was chromatographed (silica gel, hexane/ethyl acetate, 6/4) to give 2-(4-chlorophenyl)-4-(4-methoxyphenyl)-1-[4-(methylsulfonyl)phenyl]-4-(4-methoxyphenyl)-1H-imidazole (695 mg, 71%) as a white solid: mp 110°-113° C. Anal Calc'd. for C23H19N2SO3Cl: C, 62.94, H, 4.36, N, 6.38, S, 7.30. Found: C, 62.54, H, 4.43, N, 6.17, S, 7.15.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05616601
출처 데이터셋uspto-grants-1997_04
ORD IDord-aca2362d63d54cfc995742bd8c875585
출처 메모uspto-grants-1997_04