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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 518242생성일: 2026년 10월 27일

(S)-3-(1-((2-amino-5-iodopyrimidin-4-yl)amino)ethyl)-8-chloro-2-phenylisoquinolin-1(2H)-one → (S)-2-amino-4-((1-(8-chloro-1-oxo-2-phenyl-1,2-dihydroisoquinolin-3-yl)ethyl)amino)pyrimidine-5-carbonitrile

https://huagongshe.com/reaction/518242

반응식

참여 물질

역할이름HCID투입량
반응물(S)-3-(1-((2-amino-5-iodopyrimidin-4-yl)amino)ethyl)-8-chloro-2-phenylisoquinolin-1(2H)-oneHCID 71270099—
반응물HCID 178418546HCID 178418546—
촉매Copper iodideHCID 83717—
촉매Tetrakis(triphenylphosphine)palladiumHCID 11979704—
용매DimethylformamideHCID 6228—
생성물(S)-2-amino-4-((1-(8-chloro-1-oxo-2-phenyl-1,2-dihydroisoquinolin-3-yl)ethyl)amino)pyrimidine-5-carbonitrileHCID 67950671—

반응 조건

온도80 °C

반응 단계

To a solution of (S)-3-(1-((2-amino-5-iodopyrimidin-4-yl)amino)ethyl)-8-chloro-2-phenylisoquinolin-1(2H)-one 7 (700 mg, 1.35 mmol) in DMF (40 mL), cyanocopper (243 mg, 2.7 mmol), tetrakis(triphenylphosphine) palladium(0) (779 mg, 0.68 mmol), and copper iodide (180 mg, 0.95 mmol) were added and the resulting mixture was stirred at 80° C. for 16 h. The mixture was allowed to cool to RT, quenched with water and extracted with ethyl acetate (2×50 mL). The combined organic layers were washed with brine, dried over Na2SO4 and filtered. The filtrate was concentrated in vacuo and the residue was purified by flash column chromatography on silica gel eluting with 0-10% MeOH-DCM to afford the product, (S)-2-amino-4-((1-(8-chloro-1-oxo-2-phenyl-1,2-dihydroisoquinolin-3-yl)ethyl)amino)pyrimidine-5-carbonitrile 8.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09115141B2
출처 데이터셋uspto-grants-2015_08
ORD IDord-05584028b714465b8707919030afc6de
출처 메모uspto-grants-2015_08