돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 15931생성일: 2026년 10월 25일

Cesium carbonate → 4-(2-Fluoro-4-methylphenylamino)-1,2,5-trimethyl-6-oxo-1,6-dihydropyridine-3-carboxylic acid ethyl ester

https://huagongshe.com/reaction/15931

반응식

참여 물질

역할이름HCID투입량
반응물Cesium carbonateHCID 10796—
반응물2-Fluoro-4-methylanilineHCID 67984—
반응물4-Chloro-1,2,5-trimethyl-6-oxo-1,6-dihydropyridine-3-carboxylic acid ethyl esterHCID 66673972—
반응물(+/-)-2,2-Bis(diphenylphosphino)-1,1-binaphthylHCID 86595863—
촉매palladium(II) acetateHCID 167845—
용매TolueneHCID 1140—
용매Ethyl AcetateHCID 8857—
생성물4-(2-Fluoro-4-methylphenylamino)-1,2,5-trimethyl-6-oxo-1,6-dihydropyridine-3-carboxylic acid ethyl esterHCID 6667463171%

반응 조건

온도80 °C

반응 단계

2-Fluoro-4-methylphenylamine (0.259 g, 2.07 mmol), palladium (II) acetate (0.046 g, 0.205 mmol), rac-2,2-bis(diphenylphosphino)-1,1′-binaphthyl (0.192 g, 0.308 mmol), and cesium carbonate (1.00 g, 3.08 mmol) were added to a solution of 4-chloro-1,2,5-trimethyl-6-oxo-1,6-dihydropyridine-3-carboxylic acid ethyl ester (0.50 g, 2.05 mmol) in toluene (7 mL) in a sealed vial. After stirring 10 minutes, the mixture was heated to 80° C. After 24 hours, the reaction mixture was cooled to room temperature and diluted with EtOAc. The resulting precipitate was filtered and washed with EtOAc. The filtrate was diluted with EtOAc and washed with water. The aqueous layer was reextracted with EtOAc. The combined organic layers were washed with brine, dried (Na2SO4) and concentrated. Purification by flash column chromatography (20:1 methylene chloride/MeOH) gave 0.048 g (71%) desired product.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07732616B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-e69eff02af2941c1807202bb1f188821
출처 메모uspto-grants-2010_06