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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2050016Generated: November 2, 2026

Water → 2-Amino-6-chloro-9-(2-benzoyloxyethoxymethyl)purine

https://huagongshe.com/reaction/2050016

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant2-(Chloromethoxy)ethyl benzoateHCID 2724500—
Reactant2-Amino-6-chloropurineHCID 5360349—
SolventDimethylformamideHCID 6228—
Product2-Amino-6-chloro-9-(2-benzoyloxyethoxymethyl)purineHCID 1378574719.6%

Reaction Steps

A suspension of potassium carbonate (4.1 g) and 2-amino-6-chloropurine (5.0 g) in dry dimethylformamide (120 ml) was stirred for 20 minutes. 2-Benzoyloxyethoxymethyl-chloride (6.3 g) was added and the resulting pink suspension stirred at room temperature for 6 days. The reaction mixture was then poured into a mixture of ice and water (210 ml) with vigorously stirring. The aqueous mixture was extracted with chloroform (3×200 ml), and the chloroform solution obtained was washed with a 5% acetic acid solution and then twice with water. The chloroform solution was dried over anhydrous sodium sulfate and evaporated in vacuo. The residue was redissolved in a minimal amount of chloroform and the resulting solution applied to a column containing silica gel (200 g) in chloroform. The column was eluted with 2% methanol/98% chloroform and the eluant collected in 30 ml cuts. The fractions containing 2-amino-6-chloro-9-(2-benzoyloxyethoxymethyl)purine (determined by TLC) were combined, evaporated and the residue recrystallized from benzene to give 2-amino-6-chloro-9-(2-benzoyloxyethoxymethyl)purine (2.0 g., m.p. 130°-133.5° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04199574
Source datasetuspto-grants-1980_04
ORD IDord-3b63f580342146d2a17fdbc11f41e5da
Source noteuspto-grants-1980_04