반응 #461071

반응 방정식

4,6-dichloro-5-formamidopyrimidine

diethyl [4-(t-butyldimethylsilyloxy)-3-(aminooxy)butyl]phosphonate

triethylamine

→

title compound

수율 28.8%

6-[[1-(t-Butyldimethylsilyloxymethyl)-3-(diethoxyphosphoryl)propoxy]amino]-4-chloro-5-formamidopyrimidine

수율 28.8%

용매

dioxan

반응 조건

후처리

1. 1
   온도After cooling to ambient temperature
2. 2
   여과the mixture was filtered
3. 3
   기타the filtrate evaporated
4. 4
   기타The residue was chromatographed on silica gel

실험 절차

A mixture of 4,6-dichloro-5-formamidopyrimidine (0.73 g, 3.8 mmol), diethyl [4-(t-butyldimethylsilyloxy)-3-(aminooxy)butyl]phosphonate (1.35 g, 3.8 mmol) and triethylamine (0.78 ml, 5.7 mmol) in dioxan (20 ml) was heated at 90° C. for 3 hours. After cooling to ambient temperature, the mixture was filtered and the filtrate evaporated. The residue was chromatographed on silica gel using dichloromethane-methanol (98:2) as eluant to yield the title compound as a oil (0.56 g, 29). IR: υmax (film) 3180, 2940, 2870, 1690, 1635, 1250, 1030, 970, 830, 780 cm-1. 1H NMR: δH (CDCl3) 0.05 (6H, s, SiMe2), 0.9 (9H, s, SiBut), 1.3 (6H, t, J=7Hz, (OCH2CH3 )2), 1.6-2.3 (4H, m, CH2CH2P), 3.6-4.3 (7H, m, OCH2CH+(OCH2CH3)2), 7.3-10.05 (4H, broad, --NHCHO+--NHO+H-2).

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