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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1011059생성일: 2026년 10월 25일

Potassium Carbonate → 2-[(2-Cyclopropylethyl)oxy]-8-(methoxy)-9-(tetrahydro-3-furanylmethyl)-9H-purin-6-amine

https://huagongshe.com/reaction/1011059

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물(Tetrahydrofuran-3-yl)methyl methanesulfonateHCID 22273010—
반응물2,6-Dichloro-9-(tetrahydro-2H-pyran-4-ylmethyl)-9H-purineHCID 57699703—
반응물HCID 178494009HCID 178494009—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물2-[(2-Cyclopropylethyl)oxy]-8-(methoxy)-9-(tetrahydro-3-furanylmethyl)-9H-purin-6-amineHCID 57699658—

반응 조건

온도60 °C

반응 단계

To a solution of 2-[(2-cyclopropylethyl)oxy]-8-(methoxy)-1H-purin-6-amine trifluoroacetic acid salt (2.89 g) in dry N,N-dimethylformamide (32 ml) under nitrogen and at room temperature, was added potassium carbonate (4.41 g) in one go. The reaction was heated to 60° C. and stirred for 90 minutes. A solution of tetrahydro-3-furanylmethyl methanesulfonate, Isomer 2 (1.869 g) in dry DMF (3 ml) was then added gradually via pipette. The reaction was heated to 70° C. and left to stir overnight. Still 22% starting material present by LCMS, therefore increased temperature to 90° C. and stirred for a further 3 hours at this temperature. The reaction was cooled and diluted with ethyl acetate (100 ml) and washed with water (50 ml) and brine (50 ml). The organic layer was concentrated in vacuo to yield an orange oil. The product was purified by C18 reverse phase chromatography using water (0.1% formic acid)-acetonitrile (0.05% formic acid) as eluant (10-60%) to afford the title compound as an orange viscous oil (1.45 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07977344B2
출처 데이터셋uspto-grants-2011_07
ORD IDord-2d8d1935695d4250bc0ecc620c7eaee5
출처 메모uspto-grants-2011_07