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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2198914Generated: November 1, 2026

Adenosine → Acyclovir

https://huagongshe.com/reaction/2198914

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAdenosineHCID 60961—
Reactant2,6-Diamino-9-(2-hydroxyethoxymethyl)purineHCID 94588—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventAmmonium SulfateHCID 6097028—
ProductAcyclovirHCID 135398513—

Reaction Steps

To a solution of 2-amino-9-(2-hydroxyethoxymethyl)adenine (0.22 g) in water (30 ml) was added a suspension of adenosine deaminase in aqueous ammonium sulfate (0.44 ml, containing 4.4 mg of the enzyme). The reaction mixture, which initially had a pH of 7.0, was heated at 37° C. for 18 hours, at which time the pH was 8.5 and TLC (silica gel plates developed in 15% methanol - 85% chloroform) indicated a single product different from starting material. The reaction mixture was thoroughly chilled in an ice bath and the resulting white solid removed by filtration and thoroughly washed with cold water. The product was dried at 100° C./0.1 mm Hg for 16 hours to give 0.20 g of 9-(2-hydroxyethoxymethyl)guanine. 1/4 H2O, the structure of which was confirmed by m.p., TLC, U.V., NMR and mass spectroscopy analysis. Recrystallization from methanol gave the anhydrous 9-(2-hydroxyethoxymethyl)guanine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04360522
Source datasetuspto-grants-1982_11
ORD IDord-afb2ddcc581f4876a53e762b0f5894ea
Source noteuspto-grants-1982_11