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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 868639Generated: October 25, 2026

Hydrogen Peroxide → 1-Acetoxy-6-amino-1,2-dihydro-2-imino-4-(4-toluenesulfonyloxy)pyrimidine

https://huagongshe.com/reaction/868639

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 12661239HCID 12661239—
SolventEthanolHCID 702—
Product1-Acetoxy-6-amino-1,2-dihydro-2-imino-4-(4-toluenesulfonyloxy)pyrimidineHCID 22164170—

Reaction Conditions

Temperature60 °C

Reaction Steps

2.8 g (0.001 mole) of 2,6-diamino-4-tosyloxypyrimidine are added to 70 ml of absolute ethanol. 5 ml of a 70% aqueous hydrogen peroxide solution are added to the obtained suspension at 40° C., then 3 ml of acetic anhydride are added dropwise. The suspension is homogenised by heating to 60° C., and the solution gets slowly opalescent while standing. Tracing the reaction by thin layer chromatography it will be found that the reaction has completed and the aimed compound is accompanied by some diacetyl compound. By filtering the reaction mixture 0.35 g of a solid material is separated. If the ethyl alcohol is distilled off and the residue is allowed to stand in a refrigerator, no product separation can be observed. Of decanting the water and dissolving the residue in ethanol a crystalline product is obtained. In this way 1.95 g (54%) of the aimed compound are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04780537
Source datasetuspto-grants-1988_10
ORD IDord-ee61d2b4999d42c59e3023196be5d79d
Source noteuspto-grants-1988_10