Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Dimethyl Sulfate | HCID 6497 | — |
| Reactant | Lithium hydride | HCID 62714 | — |
| Reactant | HCID 178499098 | HCID 178499098 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 21098180 | HCID 21098180 | — |
Reaction Steps
To methyl 5-(benzoyloxy)-2-{(2S,4R)-1-[(benzyloxy)carbonyl]-4-methoxypyrrolidin-2-yl}-6-hydroxypyrimidine-4-carboxylate, dissolved in dioxane, LiH (1.4 eq.) was added and the reaction mixture stirred at 38° C. for 40 minutes. The temperature was raised to 60° C. and dimethyl sulphate (1.3 eq.) was added dropwise. After two hours the reaction mixture was cooled down to 0° C. and HCl 1 N was added to quench the reaction. The reaction mixture was extracted with ethyl acetate and the organic phase washed with HCl 1N, saturated aqueous NaHCO3 and brine, dried on Na2SO4, filtered and concentrated in vacuo. The desired product was isolated by flash chromatography on silica gel (eluent ethyl acetate: petroleum ether=30:70) as a 1:1 mixture of rotamers by NMR:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07820660B2 |
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| Source dataset | uspto-grants-2010_10 |
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| ORD ID | ord-19b24e2ef436496ab7539c2c85f7aee8 |
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| Source note | uspto-grants-2010_10 |
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