Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Triphenylphosphine | HCID 11776 | — |
| Edukt | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Edukt | HCID 10399205 | HCID 10399205 | — |
| Edukt | 9-Hydroxy-6-phthalimidopurine | HCID 14523970 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | HCID 10255381 | HCID 10255381 | 80,1% |
Reaktionsschritte
To a mixture of 9-hydroxy-6-phthalimidopurine (141 mg, 500 μmol), diisopropyl (E)-4-hydroxybut-1-enylphosphonate (110 g, 500 μmol) and triphenylphosphine (197 mg, 750 μmol) in tetrahydrofuran (5 ml) stirred at 0° C. was added diethyl azodicarboxylate (131 mg, 750 μmol). The mixture was then stirred at room temperature for 2 hr. The solvent was removed and the residue purified by column chromatography on silica gel eluting with dichloromethane-methanol (49:1, 16:1) to give (E)-9-[4-(diisopropoxyphosphoryl)but-3-enyloxy]-6-phthalimidopurine as a gum (200 mg, 80%); λmax (EtOH) 273 (14,380) nm; υmax (film) 2970, 1730 1590 1570 1355 1240 and 975 cm-1 ; δH [(CD3)2SO] 1.24 (12H, pseudo t, J 6 Hz, CH(CH3)2), 2.77 (2H, m, CH2), 4 60 (2H, m, CH(CH3)2), 4.66 (2H, t, J 6 Hz, CH2O ), 6.07 (1H, dd, J 17 Hz and 20 Hz, PCH=CH), 6.75 (1H, ddt, J 6 Hz, 17 Hz and 22 Hz, PCH=CH), 8.00-8.25 (4H, m, Ph), 9.00 (1H, s, H-2/H-8), 9.08 (1H, s, H-2/H-8) (Found: M+ 499. 1620. C23H26N5O6P requires M+ 499.1621).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05356886 |
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| Quelldatensatz | uspto-grants-1994_10 |
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| ORD ID | ord-c8fc4f318b8f4baeb437446062b6ae15 |
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| Quellennotiz | uspto-grants-1994_10 |
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