HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Acetate → Acyclovir
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | 9-(2-Acetoxyethoxymethyl)guanine | HCID 135446930 | — |
| Product | Acyclovir | HCID 135398513 | — |
Reaction Steps
A process for the synthesis of 9-(2-hydroxyethoxy methyl) guanine, comprising reacting guanine, or a salt thereof with between 2 and 4 moles of hexamethyldisilazane, in the presence of an aprotic solvent and of a catalytic amount of ammonium sulphate; reacting the resulting guanine trimethylsilyl derivative, without being isolated, with a stoichiometric quantity of acyloxyethoxy methyl halide at a temperature of 50° to 100° C.; and hydrolyzing with a sodium acetate or sodium hydroxyde water solution the resulting 9-(2-acetoxyethoxy methyl) guanine, to provide 9-(2-hydroxyethoxy methyl) guanine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05496945 |
| Source dataset | uspto-grants-1996_03 |
| ORD ID | ord-06aadb4eb48f4ff38cca468048f2905b |
| Source note | uspto-grants-1996_03 |