Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 136347822 | HCID 136347822 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 69314207 | HCID 69314207 | — |
Reaction Steps
To a suspension of 2-methoxy-5-(2-hydroxyethyl)-6-methyl-3H-pyrimidin-4-one (2.6 g, 0.014 mol) in DMF (25 ml) was added one equivalent of sodium hydride (55%, 0.6 g). After stirring for 0.5 hr. methyl iodide (0.81 ml, 0.014 mol) was added and the mixture was heated at 50° C. for five hours. After cooling, most of the DMF was removed in vaccuum. Water was added and the mixture was extracted with ethyl acetate. The combined organic layer was dried over sodium sulfate and then concentrated. Yield 2.0 g (71%) of a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07371769B2 |
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| Source dataset | uspto-grants-2008_05 |
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| ORD ID | ord-65867f87b4da4c0986d382242d12f61d |
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| Source note | uspto-grants-2008_05 |
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