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HRID 1716372作成日:2026年10月27日

Bromotrimethylsilane → Tenofovir

https://huagongshe.com/reaction/1716372

反応式

関与物質

役割名称HCID仕込み量
反応物BromotrimethylsilaneHCID 76113—
反応物9-(2-Hydroxypropyl)adenine, (R)-HCID 445211—
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DimethylformamideHCID 6228—
生成物TenofovirHCID 46420563.5%

反応条件

温度65 °C

反応手順

(R)-9-[2-(hydroxy)propyl]adenine (HPA) (20.0 g, 0.104 mol) was suspended in DMF (44.5 ml) and heated to 65° C. Magnesium t-butoxide (14.2 g, 0.083 mol), or alternatively magnesium isopropoxide, was added to the mixture over one hour followed by diethyl p-toluenesulfonyloxymethylphosphonate (66.0 g, 0.205 mol) over two hours while the temperature was kept at 78° C. The mixture was stirred at 75° C. for 4 hours. After cooling to below 50° C., bromotrimethylsilane (73.9 g, 0.478 mol) was added and the mixture heated to 77° C. for 3 hours. When complete, the reaction was heated to 80° C. and volatiles were removed via atmospheric distillation. The residue was dissolved into water (120 ml) at 50° C. and then extracted with ethyl acetate (101 ml). The pH of the aqueous phase was adjusted to pH 1.1 with sodium hydroxide, seeded with authentic (R)-PMPA, and the pH of the aqueous layer was readjusted to pH 2.1 with sodium hydroxide. The resulting slurry was stirred at room temperature overnight. The slurry was cooled to 4° C. for three hours. The solid was isolated by filtration, washed with water (60 ml), and dried in vacuo at 50° C. to yield 18.9 g (63.5%) of crude (R)-9-[2-(phosphonomethoxy)propyl]adenine (PMPA) as an off-white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07803788B2
出典データセットuspto-grants-2010_09
ORD IDord-44a8448e4cd146d5b2ab80c040935c1b
出典メモuspto-grants-2010_09