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HRID 345057Erstellt: 26. Oktober 2026
4-Chloro-6-[3-(diethoxyphosphorylmethoxy)propoxyamino]-2,5-diformamidopyrimidine → 6-Chloro-9-[3-(diethoxyphosphorylmethoxy)propoxy]-2-formamidopurine
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Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 4-Chloro-6-[3-(diethoxyphosphorylmethoxy)propoxyamino]-2,5-diformamidopyrimidine | HCID 19993528 | — |
| Lösungsmittel | Methanol, 1,1-diethoxy-, 1-acetate | HCID 84166 | — |
| Produkt | 6-Chloro-9-[3-(diethoxyphosphorylmethoxy)propoxy]-2-formamidopurine | HCID 19993506 | 69,2% |
Reaktionsschritte
A solution of 4-chloro-6-[3-(diethoxyphosphorylmethoxy)propoxyamino]-2,5-diformamidopyrimidine (4.48 g, 10 mmol) in diethoxymethyl acetate (40 ml) was heated at 120° C. for 2.5 h. After removal of the solvent in vacuo. the residue was dissolved in methanol (50 ml) and 0.88 ammonia (2 ml) then stirred at 25° C. for 2 h. The reaction was then reduced in vacuo and co-evaporated twice with methanol before chromatography of the residue in chloroform/methanol (100:1) to give 6-chloro-9-[3-(diethoxyphosphorylmethoxy)propoxy]-2-formamidopurine (2.92 g, 69.2%) as a yellow oil. νmax (film) 3117,1709, 1612, 1577, 1508, 1244, 1027 cm-1 ; δH [(CD3)2SO] 1.23(6H, t, J7 Hz,(CH3CH2O)2), 1.97(2H, m, CH2CH2CH2), 3.74(2H, t, J6.1Hz, CH2OCH 2 P), 3 84(2H, d, J8.0 Hz, CH2P), 4.04(4H, m, (CH3CH2O)2), 4.48(2H, t, J6.3 Hz, CH2ON), 8.83(1H, s, H-8), 9.37(1H, br.s, CHO), 11.30(1H, br.s, D2O exchangeable, NH); Found: C, 40.05; H, 5.22; N, 16.85%; M+, 421.0921. C14H23ClN5O7P requires: C, 39.87; H, 5.02; N, 16.60%; M+, 421.0918.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05055458 |
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| Quelldatensatz | uspto-grants-1991_10 |
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| ORD ID | ord-62d1f18ed92f4e7598f949f69fae170f |
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| Quellennotiz | uspto-grants-1991_10 |
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