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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 74469생성일: 2026년 10월 23일

Sodium Bicarbonate → HCID 178488449, 화합물

https://huagongshe.com/ko/reaction/74469

반응식

참여 물질

역할이름HCID투입량
반응물Sodium BicarbonateHCID 516892—
반응물(6-Methoxypyridin-3-yl)boronic acidHCID 2734368—
반응물HCID 178427384HCID 178427384—
촉매HCID 178418476HCID 178418476—
용매1,4-DioxaneHCID 31275—
생성물HCID 178488449HCID 178488449—

반응 단계

A mixture of dioxane (0.6 ml), [5-amino-1-(2-methyl-1H-benzimidazol-5-yl)-1H-pyrazol-4-yl]-[5-bromo-1-(toluene-4-sulfonyl)-1H-indol-2-yl]-methanone (60 mg, 0.102 mmol), dichlorobis(triphenylphosphine)palladium (II) (14 mg, 0.020 mmol), 2-methoxy-5-pyridine boronic acid (39 mg, 0.255 mmol), and an aqueous solution of 2 M sodium bicarbonate (0.255 mL, 0.51 mmol) was stirred at 140° C. for six minutes in a microwave reactor. The reaction mixture was filtered through Celite, and washed with ethyl acetate and then with methanol. The filtrate was dried over anhydrous sodium sulfate. The desiccant was removed by filtration and concentration was performed. The residue obtained was purified by amino gel chromatography (dichloromethane/methanol=99/1 to 92/8). Thus, [5-amino-1-(2-methyl-1H-benzimidazol-5-yl)-1H-pyrazol-4-yl]-[5-(6-methoxy-pyridin-3-yl)-1-(toluene-4-sulfonyl)-1H-indol-2-yl]-methanone was obtained as a pale yellow solid (54 mg, 85%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08829199B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-f6343928bf434b048c1223c3a9eaff2e
출처 메모uspto-grants-2014_09