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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1046752생성일: 2026년 10월 24일

6-chloro-9-(tetrahydro-2H-pyran-2-yl)-9H-purine → 8-Methyl-3-((methyl(9-(tetrahydro-2H-pyran-2-yl)-9H-purin-6-yl)amino)methyl)-2-o-tolylisoquinolin-1(2H)-one

https://huagongshe.com/ko/reaction/1046752

반응식

참여 물질

역할이름HCID투입량
반응물6-chloro-9-(tetrahydro-2H-pyran-2-yl)-9H-purineHCID 97740—
반응물8-Methyl-3-((methylamino)methyl)-2-o-tolylisoquinolin-1(2H)-oneHCID 58008619—
용매EthanolHCID 702—
생성물8-Methyl-3-((methyl(9-(tetrahydro-2H-pyran-2-yl)-9H-purin-6-yl)amino)methyl)-2-o-tolylisoquinolin-1(2H)-oneHCID 5800857051%

반응 단계

8-Methyl-3-((methylamino)methyl)-2-o-tolylisoquinolin-1(2H)-one (233 mg, 0.8 mmol) (4001) and 6-chloro-9-(tetrahydro-2H-pyran-2-yl)-9H-purine (4002) (238 mg, 1.0 mmol) were dissolved in EtOH (50 mL) and the resulting mixture was stirred at reflux for 2 h. The mixture was allowed to cool to RT, and concentrated in vacuo. The residue was purified by flash column chromatography on silica gel (2-20% MeOH/DCM) to afford the product, 8-Methyl-3-((methyl(9-(tetrahydro-2H-pyran-2-yl)-9H-purin-6-yl)amino)methyl)-2-o-tolylisoquinolin-1(2H)-one (4003) (200 mg, 51% yield) as a slight yellow solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08569323B2
출처 데이터셋uspto-grants-2013_10
ORD IDord-0ef22b5b6acd478cbaf376bc398668f9
출처 메모uspto-grants-2013_10