Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1010929생성일: 2026년 10월 25일
Potassium Carbonate → N2-Butyl-8-methoxy-9-(tetrahydro-2H-pyran-4-ylmethyl)-9H-Purine-2,6-diamine
https://huagongshe.com/reaction/1010929
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | 4-(Bromomethyl)oxane | HCID 2773286 | — |
| 반응물 | HCID 178448879 | HCID 178448879 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | N2-Butyl-8-methoxy-9-(tetrahydro-2H-pyran-4-ylmethyl)-9H-Purine-2,6-diamine | HCID 57699729 | 90% |
반응 단계
To a solution of N2-butyl-8-methoxy-9H-purine-2,6-diamine trifluoroacetic acid salt (500 mg) in dry N,N-dimethylformamide (8 ml) at room temperature and under nitrogen was added potassium carbonate (1.17 g) in one go. The reaction was stirred at 60° C. for 1.5 hours and then cooled to room temperature. 4-(bromomethyl)tetrahydro-2H-pyran (0.3 ml) was added in one go and the reaction heated at 50° C. overnight. The reaction was diluted with ethyl acetate (20 ml) and washed with water (10 ml). The organic layer was separated and concentrated in vacuo. The product was purified by C18 reverse phase chromatography using water (containing 0.1% formic acid)-acetonitrile (containing 0.05% formic acid) as eluant (10-45%) to afford the title compound as a yellow viscous oil (315 mg, 90% clean).
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-2e0643ede0dc4b8686af97d8e6ad8ca4 |
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| 출처 메모 | uspto-grants-2011_07 |
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