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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 524344생성일: 2026년 10월 23일

Potassium Carbonate → 1-Isopropyl-2-methyl-4-oxo-2'-trifluoromethyl-1,4-dihydro-[3,4]bipyridinyl-5-carboxylic acid 4-methanesulfonyl-benzylamide

https://huagongshe.com/ko/reaction/524344

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물2-(Trifluoromethyl)pyridine-4-boronic acidHCID 45158880—
반응물HCID 86711578HCID 86711578—
용매AcetonitrileHCID 6342—
생성물1-Isopropyl-2-methyl-4-oxo-2'-trifluoromethyl-1,4-dihydro-[3,4]bipyridinyl-5-carboxylic acid 4-methanesulfonyl-benzylamideHCID 73296271—

반응 조건

온도75 °C

반응 단계

To a solution of 5-bromo-1-isopropyl-6-methyl-4-oxo-1,4-dihydro-pyridine-3-carboxylic acid 4-methanesulfonyl-benzylamide (preparation 5, 24 mg, 0.054 mmol), 2-(trifluoromethyl)pyridine-4-boronic acid (13 mg, 0.068 mmol), 1,1′-[bis(diphenylphosphino)ferrocene]dichloropalladium(II) (5 mg, 0.007 mmol) in acetonitrile (0.15 mL) is added 2 M aqueous K2CO3 solution (0.055 mL, 0.11 mmol). After stirring for 18 h at 75° C., the reaction mixture is filtered and purified by preparative reversed-phase HPLC (XBridge, gradient of methanol in water, 0.3% NH4OH, 60° C.). Yield: 4 mg (15% of theory); ESI mass spectrum: [M+H]+=508; Retention time HPLC: 0.88 min (Z003_001).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09340507B2
출처 데이터셋uspto-grants-2016_05
ORD IDord-310879f39c7440c39cc8a647db580f9c
출처 메모uspto-grants-2016_05