돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 68740생성일: 2026년 10월 25일

Cesium carbonate → 6-[4-(3,5-dimethyl-piperazin-1-yl)-phenyl]-3-ethyl-4-methoxy-1-phenyl-1H-pyrazolo[3,4-b]pyridine

https://huagongshe.com/reaction/68740

반응식

참여 물질

역할이름HCID투입량
반응물Cesium carbonateHCID 10796—
반응물2,6-DimethylpiperazineHCID 66056—
반응물Binap, (A+-)-HCID 634876—
반응물6-(4-bromophenyl)-3-ethyl-7-methyl-1-phenyl-1H-pyrazolo[3,4-b]pyridin-4(7H)-oneHCID 67448819—
촉매Ferrocene-1,1'-bis-(diphenylphosphine)HCID 635956—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
용매Dimethylformamide tolueneHCID 21735183—
생성물6-[4-(3,5-dimethyl-piperazin-1-yl)-phenyl]-3-ethyl-4-methoxy-1-phenyl-1H-pyrazolo[3,4-b]pyridineHCID 58483571—

반응 조건

온도120 °C

반응 단계

Into a 50-mL round-bottom flask purged and maintained with an inert atmosphere of nitrogen, was placed a solution of 6-(4-bromophenyl)-3-ethyl-7-methyl-1-phenyl-1H-pyrazolo[3,4-b]pyridin-4(7H)-one (100 mg, 0.24 mmol, 1.00 equiv) in toluene/DMF (2 ml/Id), 2,6-dimethylpiperazine (140 mg, 1.23 mmol, 5.01 equiv), BINAP (15.3 mg, 0.02 mmol, 0.10 equiv), Pd2(dba)3 (22.4 mg, 0.02 mmol, 0.10 equiv), Cs2CO3 (140 mg, 0.73 mmol, 2.96 equiv), dppf (9.18 mg). The resulting solution was stirred overnight at 120° C. in an oil bath. The resulting mixture was concentrated under vacuum. The residue was applied onto a silica gel column with dichloromethane/methanol (200:1-100:1) to yield 6-[4-(3,5-dimethyl-piperazin-1-yl)-phenyl]-3-ethyl-4-methoxy-1-phenyl-1H-pyrazolo[3,4-b]pyridine as a yellow solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08822447B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-988177dc72a240a68ef7f7ee98d29c80
출처 메모uspto-grants-2014_09