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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1042291생성일: 2026년 10월 25일

4-Aminobenzonitrile → 4-(5-(3-(1H-pyrazolo[3,4-d]pyrimidin-4-yl)pyridin-2-ylamino)-6-methylisoquinolin-1-ylamino)benzonitrile

https://huagongshe.com/reaction/1042291

반응식

참여 물질

역할이름HCID투입량
반응물4-AminobenzonitrileHCID 13396—
반응물Lithium HexamethyldisilazideHCID 2733832—
반응물2-(Dicyclohexylphosphino)-2'-(dimethylamino)biphenylHCID 2734217—
반응물N-(3-(1H-pyrazolo[3,4-d]pyrimidin-4-yl)pyridin-2-yl)-1-chloro-6-methylisoquinolin-5-amineHCID 59627378—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
용매Acetic AcidHCID 176—
용매DichloromethaneHCID 6344—
용매TetrahydrofuranHCID 8028—
용매TriethylamineHCID 8471—
생성물4-(5-(3-(1H-pyrazolo[3,4-d]pyrimidin-4-yl)pyridin-2-ylamino)-6-methylisoquinolin-1-ylamino)benzonitrileHCID 59627369—

반응 조건

온도100 °C

반응 단계

A mixture of N-(3-(1H-pyrazolo[3,4-d]pyrimidin-4-yl)pyridin-2-yl)-1-chloro-6-methylisoquinolin-5-amine (160 mg, 413 mmol), 4-aminobenzonitrile (53.6 mg, 454 μmol), tris(dibenzylideneacetone)dipalladium(0) (18.9 mg, 20.6 μmol) and DavePhos (17.9 mg, 45.4 mmol) in THF (3 ml) was slightly vacuumed to de-gas, and then lithium bis(trimethylsilyl)amide (1.0 M solution in THF) (1857 μl, 1857 μmol) was added and the microwave tube was sealed under N2 gas. The mixture was heated in a microwave reactor at 100° C. for 30 min. The mixture was poured into DCM (10 ml)-AcOH (0.5 ml) and stirred for 10 min, then Et3N (0.5 ml) was added. Solvent was removed under vacuum and the residue was purified by flash chromatography eluting with MeOH/DCM (1-4%) to give 4-(5-(3-(1H-pyrazolo[3,4-d]pyrimidin-4-yl)pyridin-2-ylamino)-6-methylisoquinolin-1-ylamino)benzonitrile. MS Found: (ESI pos. ion) m/z 470 (M+H+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08557830B2
출처 데이터셋uspto-grants-2013_10
ORD IDord-611d0bbcb6d248ef86692eecb1bbedda
출처 메모uspto-grants-2013_10