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HRID 6243Erstellt: 23. Oktober 2026

4-Chloro-6-[2-(diethoxyphosphorylmethoxy)ethoxyamino]-5-formamidopyrimidine → 6-Chloro-9-[2-(diethoxyphosphorylmethoxy)ethoxy]purine

https://huagongshe.com/de/reaction/6243

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-Chloro-6-[2-(diethoxyphosphorylmethoxy)ethoxyamino]-5-formamidopyrimidineHCID 14862061—
LösungsmittelMethanol, 1,1-diethoxy-, 1-acetateHCID 84166—
Produkt6-Chloro-9-[2-(diethoxyphosphorylmethoxy)ethoxy]purineHCID 1486206594%

Reaktionsschritte

A solution of 4-chloro-6-[2-(diethoxyphosphorylmethoxy)ethoxyamino]-5-formamidopyrimidine (2.4 g, 6.3 mmol) in diethoxymethyl acetate (10 ml) was heated at 120° C. for 45 minutes. After cooling to ambient temperature, the solvent was removed under reduced pressure. The residue was dissolved in methanol (15 ml) and 0.880 ammonia (1 ml). After 15 minutes, the reaction mixture was evaporated to dryness and the residue chromatographed on silica gel (eluted with dichloromethane: methanol, 98:2) to give the title compound as an oil (2.15 g, 94%). IR: νmax (film) 3100, 3070, 2995, 1600, 1570, 1440, 1395, 1335, 1250, 1220, 1170, 1030, 930, 640 cm-1. 1H NMR: δH [(CD3)2SO] 1.23 (6H,t,J=7Hz, (OCH2CH3)2), 3.88 (2H, d, J=8Hz, OCH2P), 3.89 (2H,m, CH2OCH2P), 4.0-4.1 (4H,m, (OCH2CH3)2), 4.61 (2H,m, N--OCH2), 8.82 (1H,s,H-8), 8.97 (1H,s,H-2). Found: C,38.38; H,5.10; N,15.14%. C12H18N4O5PCl. 0.5H2O requires: C,38.56; H,5.12; N,14.99%. Found: m/z 364.0703. C12H18N4O5PCl requires: m/z 364.0701.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05247085
Quelldatensatzuspto-grants-1993_09
ORD IDord-da5eb9e19a5b48feb45235011949984d
Quellennotizuspto-grants-1993_09