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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 20323생성일: 2026년 10월 24일

Potassium Carbonate → 1h-Pyrazole-3-carboxamide,4-[3-(hydroxymethyl)phenyl]-1-[(4-methoxyphenyl)methyl]-n-phenyl-

https://huagongshe.com/ko/reaction/20323

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물[3-(Hydroxymethyl)phenyl]boronic acidHCID 2734662—
반응물1h-Pyrazole-3-carboxamide,4-iodo-1-[(4-methoxyphenyl)methyl]-n-phenyl-HCID 66857314—
촉매HCID 178418851HCID 178418851—
용매Ethanol toluene waterHCID 86587398—
생성물1h-Pyrazole-3-carboxamide,4-[3-(hydroxymethyl)phenyl]-1-[(4-methoxyphenyl)methyl]-n-phenyl-HCID 66855422131.9%

반응 조건

온도120 °C

반응 단계

A mixture of 4-iodo-1-(4-methoxy-benzyl)-1H-pyrazole-3-carboxylic acid phenylamide (50 mg; 0.11 mmol), bis(tri-tert-butylphosphine)palladium (12 mg), potassium carbonate (100 mg; 0.66 mmol) and 3-(hydroxymethyl)benzene boronic acid (21 mg; 0.14 mmol) in ethanol/toluene/water (4 ml:1 ml:1 ml) was heated at 120° C. (50 W) for 15 minutes in a CEM Discover microwave synthesiser. The reaction was evaporated and the residue partitioned between ethyl acetate and brine. The ethyl acetate layer was separated, dried (MgSO4), filtered and evaporated and the crude material purified by flash column chromatography eluting with 1:2 then 2:1 ethyl acetate/hexane. Product containing fractions were combined and evaporated to give 60 mg of 4-(3-hydroxymethyl-phenyl)-1-(4-methoxy-benzyl)-1H-pyrazole-3-carboxylic acid phenylamide.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07745638B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-40de71f74413494b89cc56d776bab3ea
출처 메모uspto-grants-2010_06