참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 6-(Phenylmethoxy)-9H-purin-2-amine | HCID 4578 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | HCID 10757649 | HCID 10757649 | — |
| 반응물 | HCID 178418361 | HCID 178418361 | — |
| 용매 | Acetic Acid | HCID 176 | — |
| 용매 | Diethyl Ether | HCID 3283 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | HCID 14154536 | HCID 14154536 | 25.4% |
반응 단계
A solution of 2.41 g (10 mmole) of 2-amino-6-benzyloxypurine [M. J. Robins and R. K. Robins, J. Org. Chem., 24, 2160 (1969)] in 24 ml of dry DMF was treated with 0.44 g (11 mmole) of sodium hydride (60% dispersion in oil). The mixture was stirred under nitrogen as hydrogen was evolved. After gas evolution had ceased and a clear solution had formed, a solution of 3.46 g (11 mmole) of (±)-3-(2,2-dimethyl-1,3-dioxolan-4-yl)propyl p-toluene-sulfonate (prepared as above) in 2 ml of DMF was added. The mixture was stirred at 60° C. for 3 days. The cooled mixture was then neutralized with glacial acetic acid and concentrated in vacuo. The residue was taken up in ethyl acetate, filtered, re-concentrated and chromatographed on silica gel (elution with ethyl acetate). Evaporation of fractions containing clean product gave a residue which, on trituration with ether, yielded 975 mg (25%) of white crystals, mp 111°-112° C. The analytical batch, similarly prepared, had m.p. 115.5°-118°.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04755516 |
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| 출처 데이터셋 | uspto-grants-1988_07 |
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| ORD ID | ord-7cabf6e2e6a64bd792398e990a961e79 |
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| 출처 메모 | uspto-grants-1988_07 |
|---|