Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1011058생성일: 2026년 10월 25일
Potassium Carbonate → 2-[(2-Cyclopropylethyl)oxy]-8-(methoxy)-9-(tetrahydro-3-furanylmethyl)-9H-purin-6-amine
https://huagongshe.com/reaction/1011058
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | (Tetrahydrofuran-3-yl)methyl methanesulfonate | HCID 22273010 | — |
| 반응물 | HCID 178494009 | HCID 178494009 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 2-[(2-Cyclopropylethyl)oxy]-8-(methoxy)-9-(tetrahydro-3-furanylmethyl)-9H-purin-6-amine | HCID 57699658 | — |
반응 단계
A stirring mixture of 2-[(2-cyclopropylethyl)oxy]-8-(methoxy)-1H-purin-6-amine trifluoroacetic acid salt (2.89 g), potassium carbonate (4.41 g) and dry DMF (32 ml) was heated at 60° C. under nitrogen for 90 minutes. Tetrahydro-3-furanylmethyl methanesulfonate (1.869 g, isomer 1) was then added and stirring continued at 70° C. for 1 h, then at 90° C. for 2 h. The solvent was evaporated and the residue treated with water and extracted three times with ethyl acetate. The combined extracts were washed with water then brine, dried by passing through a hydrophobic frit and evaporated to a brown oil. This was purified on a 360 gm C18 column using water (+0.1% formic acid)/acetonitrile (+0.05% formic acid). Appropriate fractions were combined and evaporated, yield 814 mg.
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-b0363e404d744e2da1fc2e4fba064b31 |
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| 출처 메모 | uspto-grants-2011_07 |
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