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HRID 2359435생성일: 2026년 10월 26일

Dichloromethane → 2-(5-Methylpyridin-3-yl)quinoline-8-carboxylic acid

https://huagongshe.com/reaction/2359435

반응식

참여 물질

역할이름HCID투입량
반응물DichloromethaneHCID 6344—
반응물Potassium Phosphate, TribasicHCID 62657—
반응물5-Methylpyridine-3-boronic acidHCID 2762708—
반응물2-Chloroquinoline-8-carboxylic acidHCID 19026201—
촉매Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물2-(5-Methylpyridin-3-yl)quinoline-8-carboxylic acidHCID 5815461172.1%

반응 조건

온도125 °C

반응 단계

A mixture of 2-chloroquinoline-8-carboxylic acid (0.600 g, 2.8 mmol), 5-methylpyridin-3-ylboronic acid (0.410 g, 3.0 mmol), K3PO4 (1.1 g, 5.2 mmol), and Pd(dppf)Cl2.CH2Cl2 (0.10 g, 0.122 mmol) in DMF (3 mL) and water (1 mL) was microwave heated (125° C.×1 Hour). The mixture was filtered over celite and the celite cake was washed with ethyl acetate (30 mL). The filtrate was combined with 60 mL aqueous saturated NaHCO3 solution and the mixture was extracted with ethyl acetate (3×20 mL). The organic layers were combined, washed with brine, dried (MgSO4), and concentrated. The crude material was purified by flash chromatography (a gradient of 0 to 100% ethyl acetate in pentane) to obtain 2-(5-methylpyridin-3-yl)quinoline-8-carboxylic acid (0.535 g, 2.02 mmol).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08685970B2
출처 데이터셋uspto-grants-2014_04
ORD IDord-f9bb6a143c27405c83db57eab064cfba
출처 메모uspto-grants-2014_04