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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1629922생성일: 2026년 10월 25일

Ethyl Acetate → 5-(3-chlorophenyl)-1-(4-methoxybenzyl)-3-methyl-1H-pyrazolo[3,4-b]pyridine

https://huagongshe.com/reaction/1629922

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl AcetateHCID 8857—
반응물Cesium carbonateHCID 10796—
반응물2-(3-Chlorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolaneHCID 10037225—
반응물5-bromo-1-(4-methoxybenzyl)-3-methyl-1H-pyrazolo[3,4-b]pyridineHCID 57856333—
촉매HCID 178418397HCID 178418397—
용매HexaneHCID 8058—
용매1,2-DimethoxyethaneHCID 8071—
생성물5-(3-chlorophenyl)-1-(4-methoxybenzyl)-3-methyl-1H-pyrazolo[3,4-b]pyridineHCID 68388550—

반응 조건

온도100 °C

반응 단계

To a stirred solution of 5-bromo-1-(4-methoxybenzyl)-3-methyl-1H-pyrazolo[3,4-b]pyridine (7) (100 mg, 0.301 mmol, 1 eq) and 2-(3-chlorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (95) (71 mg, 0.301 mmol, 1 eq) in 1,2-dimethoxyethane (10 mL) was added Cs2CO3 (244 mg, 0.752 mmol, 25 eq) 2M aqueous solution followed by degassing, purging with N2 for 15 min and addition of Pd(PPh3)4 (13 mg, 0.012 mmol, 0.04 eq). The reaction mixture was heated at 100° C. in a sealed tube overnight. After completion of the reaction the mixture was partitioned between ethyl acetate and water and the organic layer was separated and again extracted with ethyl acetate. The combined organic layers were dried over sodium sulphate and the solvent completely distilled off to get the crude. The crude was passed through 100-200 mesh silica gel eluting the pure compound at 50% ethyl acetate in hexane as off-white coloured solid compound 96 (60 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08791112B2
출처 데이터셋uspto-grants-2014_07
ORD IDord-58afe9a6dca04b13b1440bf09b656dd3
출처 메모uspto-grants-2014_07