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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 629930Generated: October 29, 2026

2-Methoxyethanol → diethyl 4-((6-amino-2-(2-methoxyethoxy)-9H-purin-9-yl)methyl)benzylphosphonate

https://huagongshe.com/reaction/629930

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MethoxyethanolHCID 8019—
ReactantSodium hydrideHCID 24758—
Reactantdiethyl 4-((6-amino-2-chloro-9H-purin-9-yl)methyl)benzylphosphonateHCID 86667757—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Productdiethyl 4-((6-amino-2-(2-methoxyethoxy)-9H-purin-9-yl)methyl)benzylphosphonateHCID 86667758—

Reaction Conditions

Temperature120 °C

Reaction Steps

To a solution of diethyl 4-((6-amino-2-chloro-9H-purin-9-yl)methyl)benzylphosphonate (1 equiv.) in 2-methoxyethanol (0.10 M) was added sodium hydride (1.3 equiv.). The reaction mixture was then heated to 120° C. for 18 h. At this point the reaction mixture was allowed to cool to room temperature. The mixture was then diluted with water and EtOAc. This mixture was transferred to a separatory funnel and washed with water three times. The organic layer was then separated, dried over anhydrous Na2SO4 and the volatiles were removed in vacuo. The resulting residue was purified by a COMBIFLASH™ system using a gradient of 0-10% MeOH/DCM to provide the title compound in quantitative yield as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09315530B2
Source datasetuspto-grants-2016_04
ORD IDord-9bcd1f1eef8c43ddb1d25a9bf116d9a3
Source noteuspto-grants-2016_04