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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1604766Generated: November 1, 2026

Potassium Carbonate → 6-chloro-2-methyl-7H-purine

https://huagongshe.com/reaction/1604766

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant6-ChloropurineHCID 5359277—
SolventPropylene CarbonateHCID 7924—
Product6-chloro-2-methyl-7H-purineHCID 5408997—

Reaction Steps

6-Chloropurine (dried over phosphorus pentoxide, 1.13 g), MBTG (3.87 g) and freshly-dried potassium carbonate (1.5 g) are stirred in anhydrous propylene carbonate (30 ml) at room temperature for 24 hours. The dark mixture is filtered and purified by column chromatography over silica 100 g) eluting with a 0-80% gradient of ethyl acetate in chloroform. The main fraction (other than unreacted 6-chlorpurine) is dried and recrystallized from boiling ethanol to yield methyl 6-chloropurine-9-(2',3',4'-tri-O-acetyl-β-D-glucopyranuronate (312 mg) and benzylamine (171 μl) are heated together in 1-butanol (13.5 ml) at 100° C. for 1 hour. The solid dissolves readily to give a clear yellow solution. Most of the butanol is removed under vacuum to yield a whitish solid which is shaken with 5% sodium hydroxide in 50% aqueous ethanol (25 ml) for 1-2 hours at room temperature. After neutralization, the product is dried under vacuum to remove traces of butanol. Crude BA9GN sodium salt is then purified by reverse-phase chromatography as in Method 1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05994629
Source datasetuspto-grants-1999_11
ORD IDord-71a4a81d0ef542fab0a66784d9bd52a1
Source noteuspto-grants-1999_11