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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 512488생성일: 2026년 10월 24일

2-(Trifluoromethyl)pyridine-4-boronic acid → 1-[1-(4-Cyano-phenyl)-ethyl]-2-methyl-4-oxo-2'-trifluoromethyl-1,4-dihydro-[3,4']bipyridinyl-5-carboxylic acid

https://huagongshe.com/ko/reaction/512488

반응식

참여 물질

역할이름HCID투입량
반응물2-(Trifluoromethyl)pyridine-4-boronic acidHCID 45158880—
반응물1-(4-Cyano-benzyl)-6-methyl-4-oxo-5-(3-trifluoromethyl-phenyl)-1,4-dihydro-pyridine-3-carboxylic acidHCID 86711527—
반응물5-Bromo-1-(4-cyano-benzyl)-6-methyl-4-oxo-1,4-dihydro-pyridine-3-carboxylic acidHCID 86711528—
반응물5-Bromo-1-[1-(4-cyano-phenyl)-ethyl]-6-methyl-4-oxo-1,4-dihydro-pyridine-3-carboxylic acidHCID 86711530—
생성물1-[1-(4-Cyano-phenyl)-ethyl]-2-methyl-4-oxo-2'-trifluoromethyl-1,4-dihydro-[3,4']bipyridinyl-5-carboxylic acidHCID 86711531—

반응 단계

Preparation 4 is prepared following the procedure described for preparation 1d, substituting 3-(trifluoromethyl)phenylboronic acid with 2-(trifluoromethyl)pyridine-4-boronic acid and substituting preparation 1c with preparation 2b as starting material. ESI mass spectrum: [M+H]+=428; Retention time HPLC: 0.99 min (Z018_S04).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09102624B2
출처 데이터셋uspto-grants-2015_08
ORD IDord-cd409417a5054a9d81a2c873f0f2f97a
출처 메모uspto-grants-2015_08