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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 541149생성일: 2026년 10월 23일

Citric Acid → 2-(5-Methoxy-pyridin-2-yl)-benzoic acid diethylamide

https://huagongshe.com/ko/reaction/541149

반응식

참여 물질

역할이름HCID투입량
반응물Citric AcidHCID 311—
반응물Potassium Phosphate, TribasicHCID 62657—
반응물(2-(Diethylcarbamoyl)phenyl)boronic acidHCID 4190636—
반응물2-Chloro-5-methoxypyridineHCID 15169000—
용매WaterHCID 962—
용매TolueneHCID 1140—
용매Ethyl AcetateHCID 8857—
생성물2-(5-Methoxy-pyridin-2-yl)-benzoic acid diethylamideHCID 5949278728.2%

반응 조건

온도80 °C

반응 단계

Under an argon atmosphere, a mixture of tripotassium phosphate (6.24 g) and water (15 ml) was added to a mixture of 2-chloro-5-methoxy-pyridine (2.05 g), 2-(diethylcarbamoyl)benzeneboronic acid (4.65 g), 1,1′-bis(diphenylphosphino)ferrocene-palladium(II) dichloride-dichloromethane complex (0.584 g) and toluene (30 ml), and the mixture was stirred at 80° C. for 2 hr. The reaction mixture was cooled to room temperature, water (20 ml), citric acid (2.2 g) and ethyl acetate were added and the mixture was stirred and filtered through celite. The filtrate was partitioned in a separatory funnel. The organic layer was washed with saturated brine, dried over anhydrous sodium sulfate, and filtered. The filtrate was concentrated under reduced pressure and the obtained residue was purified by silica gel column chromatography (eluent: n-hexane/ethyl acetate=1/1 to 1/2) to give a roughly purified product (1.144 g) of the title compound. This product was directly used for the next reaction without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08871934B2
출처 데이터셋uspto-grants-2014_10
ORD IDord-996e065bbc964b5c82d86c73e3dba0a9
출처 메모uspto-grants-2014_10