참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Bromotrimethylsilane | HCID 76113 | — |
| 반응물 | 2-(6-Aminopurin-9-yl)ethanol | HCID 242652 | — |
| 반응물 | Diethyl P-[[[(4-methylphenyl)sulfonyl]oxy]methyl]phosphonate | HCID 4193599 | — |
| 반응물 | Magnesium dipropan-2-olate | HCID 10197750 | — |
| 반응물 | Magnesium 2-methylpropan-2-olate | HCID 12040442 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | Adefovir | HCID 60172 | 65.4% |
반응 단계
9-(2-Hydroxyethyl)adenine (HEA) (20.0 g, 0.112 mol) was suspended in is DMF (125 ml) and heated to 80° C. Magnesium isopropoxide (11.2 g, 0.0784 mol), or alternatively magnesium t-butoxide, was added to the mixture followed by diethyl p-toluenesulfonyloxymethylphosphonate (66.0 g, 0.162 mol) over one hour. The mixture was stirred at 80° C. for 7 hours. 30 ml of volatiles were removed via vacuum distillation and the reaction was recharged with 30 ml of fresh DMF. After cooling to room temperature, bromotrimethylsilane (69.6 g, 0.450 mol) was added and the mixture heated to 80° C. for 6 hours. The reaction was concentrated to yield a thick gum. The gum was dissolved into 360 ml water, extracted with 120 ml dichloromethane, adjusted to pH 3.2 with sodium hydroxide, and the resulting slurry stirred at room temperature overnight. The slurry was cooled to 4° C. for one hour. The solids were isolated by filtration, washed with water (2×), and dried in vacuo at 56° C. to yield 20 g (65.4%) of 9-[2-(phosphonomethoxy)ethyl]adenine (PMEA) as a white solid. Mp: >200° C. dec. 1H NMR (D2O) δ 3.49 (t, 2H); 3.94 (t, 2H); 4.39 (t, 2H); 8.13 (s, 1H); 8.22 (s, 1H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07803788B2 |
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| 출처 데이터셋 | uspto-grants-2010_09 |
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| ORD ID | ord-512d238eb3af46a89a2ca71a00f0bd20 |
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| 출처 메모 | uspto-grants-2010_09 |
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