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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | (Tetrahydrofuran-3-yl)methyl methanesulfonate | HCID 22273010 | — |
| 반응물 | 2,6-Dichloro-9-(tetrahydro-2H-pyran-4-ylmethyl)-9H-purine | HCID 57699703 | — |
| 반응물 | HCID 178494009 | HCID 178494009 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | 2-[(2-Cyclopropylethyl)oxy]-8-(methoxy)-9-(tetrahydro-3-furanylmethyl)-9H-purin-6-amine | HCID 57699658 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07977344B2 |
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| 출처 데이터셋 | uspto-grants-2011_07 |
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| ORD ID | ord-2d8d1935695d4250bc0ecc620c7eaee5 |
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| 출처 메모 | uspto-grants-2011_07 |
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