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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1046749생성일: 2026년 10월 24일

Sodium hydride → 3-((6-amino-9H-purin-9-yl)methyl)-8-methyl-2-o-tolylisoquinolin-1(2H)-one

https://huagongshe.com/ko/reaction/1046749

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물3-(Bromomethyl)-8-methyl-2-o-tolylisoquinolin-1(2H)-oneHCID 58008650—
반응물HCID 178508693HCID 178508693—
용매DimethylformamideHCID 6228—
생성물3-((6-amino-9H-purin-9-yl)methyl)-8-methyl-2-o-tolylisoquinolin-1(2H)-oneHCID 5800869870%

반응 단계

9H-Purin-6-amine (1901) (540 mg, 4.0 mmol) was dissolved in anhydrous DMF (20 mL). NaH (60% in mineral oil, 160 mg, 4.0 mmol) was added and the resulting mixture was stirred at RT for 30 min. 3-(Bromomethyl)-8-methyl-2-o-tolylisoquinolin-1(2H)-one (1610) (1.37 g, 4.0 mmol) was added. The reaction mixture was stirred at RT for 30 min, poured into ice-water (30 mL) and then extracted with ethyl acetate (3×50 mL). The combined organic layer was washed with brine (25 mL), dried over Na2SO4 and filtered. The filtrate was concentrated in vacuo and the residue was purified by flash column chromatography on silica gel (2-20% MeOH/DCM) to afford the desired product, 3-((6-amino-9H-purin-9-yl)methyl)-8-methyl-2-o-tolylisoquinolin-1(2H)-one (1902, compound 5 of Table 4) (1.1 g, 70% yield) as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08569323B2
출처 데이터셋uspto-grants-2013_10
ORD IDord-82dd8060384d41d3802d016f8180e736
출처 메모uspto-grants-2013_10