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HRID 133115作成日:2026年10月25日

Bromotrimethylsilane → Adefovir

https://huagongshe.com/reaction/133115

反応式

関与物質

役割名称HCID仕込み量
反応物BromotrimethylsilaneHCID 76113—
反応物2-(6-Aminopurin-9-yl)ethanolHCID 242652—
反応物Diethyl P-[[[(4-methylphenyl)sulfonyl]oxy]methyl]phosphonateHCID 4193599—
反応物Magnesium dipropan-2-olateHCID 10197750—
反応物Magnesium 2-methylpropan-2-olateHCID 12040442—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物AdefovirHCID 6017265.4%

反応条件

温度80 °C

反応手順

9-(2-Hydroxyethyl)adenine (HEA) (20.0 g, 0.112 mol) was suspended in 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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07390791B2
出典データセットuspto-grants-2008_06
ORD IDord-8cd7c6c8eaed4eedadde19e8a7176674
出典メモuspto-grants-2008_06