HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 48559Erstellt: 23. Oktober 2026
Dimethylformamide → (R)-9-[2-(N-Boc-L-valyloxymethyl)4-(stearoyloxy)butyl]guanine
https://huagongshe.com/de/reaction/48559
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Dimethylformamide | HCID 6228 | — |
| Edukt | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Edukt | Boc-L-Valine | HCID 83693 | — |
| Edukt | (R)-9-[2-Hydroxymethyl-4-(stearoyloxy)butyl]guanine | HCID 136343267 | — |
| Katalysator | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | (R)-9-[2-(N-Boc-L-valyloxymethyl)4-(stearoyloxy)butyl]guanine | HCID 135829460 | 39,3% |
Reaktionsschritte
A mixture of N-Boc-L-valine (528 mg; 2.1 mmol) and N,N′-dicyclohexyl carbodiimide (250 mg; 1.21 mg) in dichloromethane (20 ml) was stirred over night at room temperature, dicyclohexylurea filtered off and extracted with a small volume of dichloromethane, and the filtrate evaporated in vacuo to a small volume. (R)-9-[2-Hydroxymethyl-4-(stearoyloxy)butyl]guanine (340 mg; 0.654 mmol), 4-dimethylaminopyridine (25 mg; 0.205 mmol), and dry N,N-dimethylformamide (15 ml) were added and the mixture was stirred for 4 h at 50° C. under N2. The solvent was evaporated in vacuo to a small volume. Column chromatography on silica gel, then on aluminum oxide (ethyl acetate:methanol: water 15:2:1 as eluent) gave 185 mg (39%) pure title compound as a white solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06703394B2 |
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| Quelldatensatz | uspto-grants-2004_03 |
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| ORD ID | ord-fd5c64ed8b2a4ec8b5c23cabdd62366f |
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| Quellennotiz | uspto-grants-2004_03 |
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