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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 611462생성일: 2026년 10월 26일

Pyridine → Ortho-nitrobenzyladenosine

https://huagongshe.com/reaction/611462

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물Sodium hydrideHCID 24758—
반응물alpha-Bromo-2-nitrotolueneHCID 77569—
반응물2'-Deoxyadenosine monohydrateHCID 9549172—
용매DimethylformamideHCID 6228—
생성물Ortho-nitrobenzyladenosineHCID 7014678339.8%

반응 단계

2'-Deoxyadenosine monohydrate (538 mg, 2.0 mmol, Aldrich Chemical, Milwaukee, Wisc.) was dried by evaporation with anhydrous pyridine (2 times, 10 ml) under vacuum. The residue was dissolved in anhydrous DMF (10 ml, Aldrich, Milwaukee, Wisc.) under an argon atmosphere, and sodium hydride (88 mg, 2.2 mmol, 1.1 equiv, 60% dispersion in oil) was added and stirred for 40 mins at room temperature. 2-Nitrobenzyl bromide (710 mg, 3.3 mmol, 1.5 equiv) was added and the solution was stirred for 4 hours at room temperature. The DMF was removed by evaporation under vacuum, and the residue was partitioned between ethyl acetate and water (20 ml each). The aqueous phase was extracted with ethyl acetate (20 ml) and the combined extracts were washed with water (20 ml) and dried over magnesium sulfate, filtered and evaporated. The crude product was purified by column chromatography on silica gel (50 g, using 3% MeOH in CH2Cl2) to yield 2'-deoxy-N6 -bis-ortho-nitrobenzyladenosine (320 mg, 30%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06001611
출처 데이터셋uspto-grants-1999_12
ORD IDord-3c2e13034cc941bc92ba7f9e3993e05c
출처 메모uspto-grants-1999_12