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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 68737생성일: 2026년 10월 26일

Cesium carbonate → tert-butyl 4-(4-(3-methyl-4-oxo-1-phenyl-4,7-dihydro-1H-pyrazolo[3,4-b]pyridin-6-yl)phenyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/68737

반응식

참여 물질

역할이름HCID투입량
반응물Cesium carbonateHCID 10796—
반응물tert-Butyl piperazine-1-carboxylateHCID 143452—
반응물Binap, (A+-)-HCID 634876—
반응물6-(4-bromophenyl)-3-methyl-1-phenyl-1H-pyrazolo[3,4-b]pyridin-4(7H)-oneHCID 136386287—
촉매Ferrocene-1,1'-bis-(diphenylphosphine)HCID 635956—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
용매Dimethylformamide tolueneHCID 21735183—
생성물tert-butyl 4-(4-(3-methyl-4-oxo-1-phenyl-4,7-dihydro-1H-pyrazolo[3,4-b]pyridin-6-yl)phenyl)piperazine-1-carboxylateHCID 136386288—

반응 조건

온도120 °C

반응 단계

Into a 100 mL round-bottom flask purged and maintained with an inert atmosphere of nitrogen, was placed a solution of 6-(4-bromophenyl)-3-methyl-1-phenyl-1H-pyrazolo[3,4-b]pyridin-4(7H)-one (2500 mg, 6.58 mmol, 1.00 equiv) in toluene/DMF (30 ml/1 ml mL), tert-butyl piperazine-1-carboxylate (6130 mg, 32.96 mmol, 5.00 equiv), BINAP (410 mg, 0.65 mmol, 0.10 equiv), Pd2(dba)3 (602.9 mg, 0.66 mmol, 0.10 equiv), Cs2CO3 (3819 mg, 19.79 mmol, 3.00 equiv), dppf (270 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 (1:10) to yield tert-butyl 4-(4-(3-methyl-4-oxo-1-phenyl-4,7-dihydro-1H-pyrazolo[3,4-b]pyridin-6-yl)phenyl)piperazine-1-carboxylate as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08822447B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-b98e8c06dc1d4e6186d03cf46e7a33e8
출처 메모uspto-grants-2014_09