돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 52303생성일: 2026년 10월 24일

2-Bromo-2'-acetonaphthone → 2-(4-chlorophenyl)-1-(4-(methylsulfonyl)phenyl]-4-(2-naphthyl)-1H-imidazole

https://huagongshe.com/ko/reaction/52303

반응식

참여 물질

역할이름HCID투입량
반응물2-Bromo-2'-acetonaphthoneHCID 69179—
반응물Sodium BicarbonateHCID 516892—
반응물4-chloro-N-[4-(methylsulfonyl)phenyl]benzenecarboximidamideHCID 178504796—
용매IsopropanolHCID 3776—
생성물2-(4-chlorophenyl)-1-(4-(methylsulfonyl)phenyl]-4-(2-naphthyl)-1H-imidazoleHCID 2214894654%

반응 단계

To a mixture of 4-chloro-N-[4-(methylsulfonyl)phenyl]benzenecarboximidamide (Example 1, Step 1) (400 mg, 1.29 mmol) and sodium bicarbonate (216 mg, 2.59 mmol) in isopropanol (30 mL), 2-bromo-2'-acetonaphthone (970 mg, 3.89 mmol) was added. After heating the reaction mixture at 80°-85° 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 (1.2 g) was chromatographed (silica gel, hexane/ethyl acetate, 6/4) to give 2-(4-chlorophenyl)-1-[4-(methylsulfonyl)phenyl]-4-(2-naphthyl)-1H-imidazole (318 mg, 54%) as a pale yellow solid: mp 204°-206° C. Anal Calc'd. for C26H19N2SO2Cl: C, 68.04, H, 4.17, N, 6.10, S, 6.99. Found: C, 67.65, H, 4.19, N, 5.96, S, 7.10.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05616601
출처 데이터셋uspto-grants-1997_04
ORD IDord-97d1a99becd14f46b6562dc20c7893bb
출처 메모uspto-grants-1997_04