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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 64376생성일: 2026년 10월 23일

Sodium Carbonate → 6-(3-Hydroxyphenyl)-2-(4-phenoxyphenyl) pyrazolo[1,5-a]pyrimidine-3-carbonitrile

https://huagongshe.com/ko/reaction/64376

반응식

참여 물질

역할이름HCID투입량
반응물Sodium CarbonateHCID 10340—
반응물(3-hydroxyphenyl)boronic AcidHCID 2734359—
반응물6-Bromo-2-(4-phenoxyphenyl)pyrazolo[1,5-a]pyrimidine-3-carbonitrileHCID 117668092—
촉매HCID 178418397HCID 178418397—
용매WaterHCID 962—
용매1,4-DioxaneHCID 31275—
생성물6-(3-Hydroxyphenyl)-2-(4-phenoxyphenyl) pyrazolo[1,5-a]pyrimidine-3-carbonitrileHCID 11766810962%

반응 조건

온도65 °C

반응 단계

To a solution of 6-bromo-2-(4-phenoxyphenyl)pyrazolo[1,5-a]pyrimidine-3-carbonitrile (782 mg, 2.0 mmol) in dioxane (10 mL) and H2O (10 mL) was added 3-hydroxyphenylboronic acid (276 mg, 2.0 mmol), Pd(PPh3)4 (240 mg, 0.2 mmol) and Na2CO3 (424 mg, 4.0 mmol). After stirring at 65° C. under N2 for 16 hr, the mixture was concentrated and 100 mL of DCM, 10 mL of CH3OH, 100 mL of H2O were added. Organic layers were separated from aqueous layers and dried over Na2SO4 and purified by chromatography column on silica gel eluting with DCM/CH3OH to afford 500 mg (62%) of 6-(3-hydroxyphenyl)-2-(4-phenoxyphenyl) pyrazolo[1,5-a]pyrimidine-3-carbonitrile as a yellow solid. MS (ESI) m/e [M+1]+ 404.9.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09447106B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-ef099b0ab4d746cc97e8ec35a5a8e201
출처 메모uspto-grants-2016_09