Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Adenine | HCID 190 | — |
| Edukt | Methanesulfonic Acid | HCID 6395 | — |
| Edukt | Tenofovir | HCID 464205 | — |
| Edukt | (4R)-4-methyl-1,3-dioxolan-2-one | HCID 641813 | — |
| Edukt | Magnesium 2-methylpropan-2-olate | HCID 12040442 | — |
| Katalysator | Sodium Hydroxide | HCID 14798 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 9-(2-Hydroxypropyl)adenine, (R)- | HCID 445211 | 75% |
Reaktionsschritte
Adenine to PMPA using Magnesium t-Butoxide. To a suspension of adenine (40 g, 0.296 mol) in DMF (41.9 ml) was added (R)-propylene carbonate (34.5 g, 0.338 mol) and sodium hydroxide (0.480 g, 0.012 mol). The mixture was heated at 130° C. overnight. The reaction was cooled to 100° C. and toluene (138 ml) was added followed by methanesulfonic acid (4.7 g, 0.049 mol) while maintaining the reaction temperature between 100-110° C. Additional toluene (114 ml) was added to create a homogeneous solution. The solution was cooled to 3° C. over 7 hours and then held at 3° C. for one hour. The resulting solid was isolated by filtration and rinsed with acetone (2×). The wet solid was dried in vacuo at 80° C. to yield 42.6 g (75%) of (R)-9-[2-(hydroxy)propyl]adenine (HPA) as an off-white solid. Mp: 188-190° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07390791B2 |
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| Quelldatensatz | uspto-grants-2008_06 |
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| ORD ID | ord-a8c4279c99924b52a3123195564751d5 |
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| Quellennotiz | uspto-grants-2008_06 |
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