Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Acyclovir | HCID 135398513 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 135754930 | HCID 135754930 | — |
Reaction Steps
To a stirred solution of 9-(2-hydroxyethoxymethyl)guanine (1.0 g; 4.44 mmol) in dry DMF (50 ml) was added a solution of methyl iodide (680 mg, 4.77 mmol) in dry DMF (2 ml). This mixture was heated under a reflux condenser under N2 at 57° C. overnight. The mixture was concentrated in vacuo to an oil and the evaporation was repeated several times from MeOH. The residue was dissolved in MeOH (20 ml) and 2-propanol (150 ml) was added and the mixture was stirred overnight. A yellow solid was obtained which was filtered off (200 mg). This was recrystallized from MeOH (25 ml) (solution filtered through a little charcoal). Crystallization was induced by concentration of the solution, cooling and by the addition of a little 2-propanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04579849 |
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| Source dataset | uspto-grants-1986_04 |
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| ORD ID | ord-36bcc96d981b42a0bc9f15cecbbe175a |
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| Source note | uspto-grants-1986_04 |
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