Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Water → 9-((2-Acetoxyethoxy)methyl)-6-chloropurine
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Water | HCID 962 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | 2-(Bromomethoxy)ethyl acetate | HCID 367656 | — |
| 반응물 | 6-Chloropurine | HCID 5359277 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 9-((2-Acetoxyethoxy)methyl)-6-chloropurine | HCID 512655 | 68% |
반응 단계
To a solution of 6-chloropurine (6 g, 38.8 mmoles) in DMF was added sodium hydride 60% (0.93 g) over 1.5 hour period. (2-acetoxyethoxy)methyl bromide was then added at room temperature; the reaction mixture was allowed to stir for 2 hours under Nz atmosphere. H2O was added and the product was extracted with ethyl acetate. The organic phase was dried over MgSO4, filtered, and evaporated in vacuo to give a light yellow solid 7.1 g, 68% yield of 9-[(2-acetoxy-ethoxy)methyl]-6-chloro-purine. The crude was used without further purification.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US05117830 |
| 출처 데이터셋 | uspto-grants-1992_06 |
| ORD ID | ord-f44e10d4426d48e2be129f56c37ce4e1 |
| 출처 메모 | uspto-grants-1992_06 |