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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 82039생성일: 2026년 10월 23일

Cesium carbonate → 6-(4-hydroxy-phenyl)-1-(tetrahydro-pyran-2-yl)-3-vinyl-1H-pyrazolo[3,4-b]pyridine-4-carboxylic acid

https://huagongshe.com/ko/reaction/82039

반응식

참여 물질

역할이름HCID투입량
반응물Cesium carbonateHCID 10796—
반응물4-Hydroxyphenylboronic acidHCID 2734360—
반응물6-chloro-1-(tetrahydro-pyran-2-yl)-3-vinyl-1H-pyrazolo[3,4-b]pyridine-4-carboxylic acid ethyl esterHCID 86678168—
촉매HCID 178418397HCID 178418397—
용매1,4-DioxaneHCID 31275—
생성물6-(4-hydroxy-phenyl)-1-(tetrahydro-pyran-2-yl)-3-vinyl-1H-pyrazolo[3,4-b]pyridine-4-carboxylic acidHCID 136359503143.7%

반응 단계

To a solution of 6-chloro-1-(tetrahydro-pyran-2-yl)-3-vinyl-1H-pyrazolo[3,4-b]pyridine-4-carboxylic acid ethyl ester (2.00 g, 5.96 mmol), described in example 16.1, in dioxane (54 mL) were added 4-hydroxyphenylboronic acid (0.90 g, 6.55 mmol) and an aqueous solution of cesium carbonate (0.4 M, 27 mL, 10.8 mmol). The resulting solution was degassed using argon, tetrakis(triphenylphosphine)palladium (0.62 g, 0.54 mmol) was then added and the reaction mixture was refluxed overnight. Dioxane was removed under vacuum, water was added and then the mixture was acidified to pH=2. The aqueous phase was extracted with a mixture of tetrahydrofuran and EtOAc. The combined organic extracts were washed with brine, dried (Na2SO4), filtered, concentrated under vacuum to give the title compound (3.13 g) as a brown foam which was used without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08846712B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-8d689576def44b3cae178a21b4357d6c
출처 메모uspto-grants-2014_09