Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Adenine | HCID 190 | — |
| Reactant | 18-Crown-6 | HCID 28557 | — |
| Reactant | HCID 14606665 | HCID 14606665 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Ro 24-5098 | HCID 124453 | 29% |
Reaction Steps
To a flame-dried argon blanketed round bottom flask equipped with a magnetic stir bar and condenser was added adenine (50 mg, 0.37 mmole) K2CO3 (100 mg, 0.73 mmole), 18-crown-6 (97 mg, 0.37 mmole) and DMF (10 mL). This mixture was allowed to stir at room temperature for 30 minutes under a stream of argon. A solution of (2R-trans)-tetrahydro-4-[[(4-methylphenyl)sulfonyl]oxy]-2-furanmethanol, Compound IV(c), (100 mg, 0.37 mmole) in 2 mL DMF was then added dropwise to the stirring mixture. The resultant mixture was warmed to 80° C., and stirred at that temperature overnight. After removal of the solvent in vacuo, the solid residue was purified by flash chromatorgraphy using a 10% MeOH/90% CH2Cl2 solution as eluant. This isolated material was further purified by reverse-phase HPLC using a gradient elution system of CH3CN/H2O to yield 25 mg (29%) of Compound I as a white solid. An analytical sample was crystallized from methanol: mp 183°-185°, [α]D +47.91 (c 0.67, MeOH).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05126347 |
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| Source dataset | uspto-grants-1992_06 |
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| ORD ID | ord-966c8465a618423ebfe0cbb64ddc7423 |
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| Source note | uspto-grants-1992_06 |
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