돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 133115생성일: 2026년 10월 24일

Bromotrimethylsilane → Adefovir

https://huagongshe.com/ko/reaction/133115

반응식

참여 물질

역할이름HCID투입량
반응물BromotrimethylsilaneHCID 76113—
반응물2-(6-Aminopurin-9-yl)ethanolHCID 242652—
반응물Diethyl P-[[[(4-methylphenyl)sulfonyl]oxy]methyl]phosphonateHCID 4193599—
반응물Magnesium dipropan-2-olateHCID 10197750—
반응물Magnesium 2-methylpropan-2-olateHCID 12040442—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물AdefovirHCID 6017265.4%

반응 조건

온도80 °C

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07390791B2
출처 데이터셋uspto-grants-2008_06
ORD IDord-8cd7c6c8eaed4eedadde19e8a7176674
출처 메모uspto-grants-2008_06