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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Bromomethyl 4-methoxyphenyl ketone | HCID 4965 | — |
| 반응물 | Sodium Bicarbonate | HCID 516892 | — |
| 반응물 | 4-chloro-N-[4-(methylsulfonyl)phenyl]benzenecarboximidamide | HCID 178504796 | — |
| 용매 | Isopropanol | HCID 3776 | — |
| 생성물 | 2-(4-chlorophenyl)-4-(4-methoxyphenyl)-1-(4-(methylsulfonyl)phenyl]-4-(4-methoxyphenyl)-1H-imidazole | HCID 22998078 | 113.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05616601 |
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| 출처 데이터셋 | uspto-grants-1997_04 |
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| ORD ID | ord-aca2362d63d54cfc995742bd8c875585 |
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| 출처 메모 | uspto-grants-1997_04 |
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