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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1693495생성일: 2026년 10월 27일

Ethyl Acetate → 5-(4-chloro-phenyl)-6-(2,4-dichlorophenyl)-1-phenyl-1H-pyrazolo[3,4-b]pyridin-4-ylamine

https://huagongshe.com/reaction/1693495

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl AcetateHCID 8857—
반응물5-Amino-1-phenyl-1H-pyrazole-4-carbonitrileHCID 79256—
반응물2-(4-Chlorophenyl)-1-(2,4-dichlorophenyl)ethan-1-oneHCID 21984867—
촉매Titanium TetrachlorideHCID 24193—
용매1,1-DichloroethaneHCID 6365—
생성물5-(4-chloro-phenyl)-6-(2,4-dichlorophenyl)-1-phenyl-1H-pyrazolo[3,4-b]pyridin-4-ylamineHCID 11619662—

반응 단계

A solution of 2-(4-chloro-phenyl)-1-(2,4-dichloro-phenyl)-ethanone (300 mg, 0.99 mmol) in dichloroethane (3 mL) is stirred at room temperature while TiCl4 (311 mg, 1.64 mmol) is added dropwise. After the addition, the mixture is stirred at room temperature for 5 minutes and a solution of 5-amino-1-phenyl-1H-pyrazole-4-carbonitrile (150 mg, 0.815 mmol) in dichloroethane (3 mL) is added dropwise. After the addition, the mixture is heated to 125° C. for 5 hours. After cooling, the mixture is poured into a mixture of ice cold saturated aqueous NaHCOs solution (30 mL) and EtOAc (30 mL). The resultant precipitate is filtered through celite and washed with EtOAc (2×10 mL). The filtrate is extracted by EtOAc (3×15 mL). The organic layers are combined and washed with brine and dried (MgSO4). After filtering off the drying agent, the filtrate is concentrated and purified by column chromatography (silica gel, 0%˜40% EtOAc/hexane) to provide the titled compound 5-(4-chloro-phenyl)-6-(2,4-dichloro-phenyl)-1-phenyl-1H-pyrazolo[3,4-b]pyridin-4-ylamine as light yellow solid:

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08158634B2
출처 데이터셋uspto-grants-2012_04
ORD IDord-e83f9a8350d541c59c0050f21c20238b
출처 메모uspto-grants-2012_04