Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | 2'-C-methyluridine | HCID 500903 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 68380776 | HCID 68380776 | 93% |
Reaction Steps
The preparation of Compound 55 is illustrated in Scheme 5, above. To a solution of 2′-C-methyluridine (1 g) in pyridine (40 ml) were added acetic acid (3 ml) and DMAP. The mixture was stirred at 50° C. during 3 hours, followed by two days at room temperature. Then, the mixture was concentrated and co-evaporated with toluene and the residue purified by silica gel chromatography eluting with 0→10% methanol in dichloromethane to yield 2′,3′,5′-Tri-O-acetyl-2′-C-methyluridine (93%). MS (ESI, EI+) m/z=385.2 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09243025B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-002641dc01614c8bb3520323e0095669 |
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| Source note | uspto-grants-2016_01 |
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