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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2354839Generated: October 29, 2026

Potassium Carbonate → HCID 178450377, compound

https://huagongshe.com/reaction/2354839

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant3-(Chloromethyl)pyridine hydrochlorideHCID 23394—
ReactantHCID 23079437HCID 23079437—
SolventDimethylformamideHCID 6228—
ProductHCID 178450377HCID 17845037753.8%

Reaction Steps

After 2-butoxy-9-(4-carboxybenzyl)-8-methoxyadenine (0.05 g, 0.13 mmol) prepared in accordance with the method of Reference example 5 and potassium carbonate (0.03 g, 0.22 mmol) were added to DMF (10 ml), 3-chloromethylpyridine hydrochloride (0.03 g, 0.18 mmol) was added thereto, and the mixture was stirred at room temperature for 18 hours. After removing the solvent, the residue was poured into water and extracted with dichloromethane. The organic layer was dried over anhydrous magnesium sulfate and concentrated. The residue was purified by column chromatography (SiO2 20 g, eluting solvent: CHCl3/MeOH=300/1˜30/1) and the resulting solid was added to methanol (10 ml) and concentrated hydrochloric acid (10 ml). The mixture was stirred at room temperature for 18 hours. After being neutralized with saturated sodium hydrogencarbonate, the solution was extracted with dichloromethane. The organic layer was dried over anhydrous magnesium sulfate, concentrated and washed with methanol to give the captioned compound (0.03 g, 0.07 mmol, yield: 52%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07754728B2
Source datasetuspto-grants-2010_07
ORD IDord-36ccce98bd754c98b24d7a7f594ca517
Source noteuspto-grants-2010_07