돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 13655생성일: 2026년 10월 24일

1-(Methylsulphonyl)acetone → 6-Bromo-3-methanesulfonyl-2-methyl-4-phenyl-quinoline

https://huagongshe.com/ko/reaction/13655

반응식

참여 물질

역할이름HCID투입량
반응물1-(Methylsulphonyl)acetoneHCID 78695—
반응물2-Amino-5-bromobenzophenoneHCID 99677—
반응물SodiumHCID 5360545—
용매IsopropanolHCID 3776—
생성물6-Bromo-3-methanesulfonyl-2-methyl-4-phenyl-quinolineHCID 1200162634%

반응 단계

(2-Amino-5-bromo-phenyl)-phenyl-methanone (10 g, 36 mmol), methanesulfonylacetone (7.4 g, 54 mmol) and sodium tetrachloroaureate(III) dihydrate (720 mg, 1.8 mmol) were heated at reflux in 2-propanol (100 mL) for 4.5 days. The resulting suspension was evaporated to dryness and the residue extracted with dichloromethane (2×), 1 N NaOH (2×), which removes excess of methanesulfonylacetone, and sat. NaCl (1×). The crude product was purified twice by chromatography in dichloromethane and then crystallized from dichloromethane/heptane by evaporation of dichloromethane. One obtained 4.6 g (33%) of beige crystals. MS: m/z=375/377 (M).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07728142B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-e1894e98006d45e997e4443d44c97654
출처 메모uspto-grants-2010_06