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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 10434생성일: 2026년 10월 25일

3,4-dihydro-2H-pyran → 2,6-Dichloro-9-(tetrahydro-2H-pyran-2-yl)-9H-purine

https://huagongshe.com/reaction/10434

반응식

참여 물질

역할이름HCID투입량
반응물3,4-dihydro-2H-pyranHCID 8080—
반응물Sodium BicarbonateHCID 516892—
반응물p-Toluenesulfonic acid monohydrateHCID 521998—
반응물2,6-dichloro-1H-purineHCID 178418875—
용매WaterHCID 962—
용매Ethyl AcetateHCID 8857—
생성물2,6-Dichloro-9-(tetrahydro-2H-pyran-2-yl)-9H-purineHCID 270265—

반응 조건

온도50 °C

반응 단계

2,6-Dichloro-9H-purine (20 g, 0.11 mol) and 4-toluenesulphonic acid monohydrate (0.2 g) were dissolved in ethyl acetate (300 ml), the mixture heated to 50° C. and a solution of 3,4-dihydro-2H-pyran (12.6 ml, 0.14 mol) in ethyl acetate (50 ml) added slowly over 30 minutes. The reaction mixture was cooled to room temperature, water (100 ml) added and the pH of the solution adjusted to 7 by addition of a saturated aqueous solution of sodium hydrogen carbonate. The organic layer was separated, washed sequentially with water and brine, dried over anhydrous magnesium sulphate, filtered and the solvent removed under reduced pressure. The residue was azeotroped with pentane (×2) to afford the title compound as a slightly impure white solid (30.9 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07094769B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-69e4a8157db7424a83d31d8e7356ee4a
출처 메모uspto-grants-2006_08