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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1253178Generated: October 30, 2026

Potassium Carbonate → Methyl 4-[(2-amino-6-chloro-9H-purin-9-yl)methyl]benzoate

https://huagongshe.com/reaction/1253178

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl 4-(bromomethyl)benzoateHCID 256687—
Reactant2-Amino-6-chloropurineHCID 5360349—
ReactantChloroform methanolHCID 21584188—
SolventDimethylformamideHCID 6228—
ProductMethyl 4-[(2-amino-6-chloro-9H-purin-9-yl)methyl]benzoateHCID 14182432—

Reaction Steps

A mixture of 2-amino-6-chloropurine (5 g, 0.029 mol), 4-(bromomethyl)benzoic acid methyl ester (6.7 g, 0.029 mol), and potassium carbonate (4.0 g, 0.029 mol) in dry DMF (75 ml) is stirred at room temperature for three days. The reaction mixture is filtered and the filtrate is evaporated to near dryness under vacuum. Water is added and the precipitate is collected by filtration to give a mixture of 7- and 9-substituted products (10.5 g). A sample of pure 9-isomer, i.e., 2-amino-9-[(4-carbomethoxyphenyl)methyl)-6-chloropurine, (mp=150°-155° C. softens, 183°-185° C. melts) is prepared by chromatography on silica gel with 5% methanol/chloroform as the eluting solvent to separate it from the slower moving 7-isomer.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04748177
Source datasetuspto-grants-1988_05
ORD IDord-1af87c1964724140b209e0d7dea9a77d
Source noteuspto-grants-1988_05