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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1453578Generated: October 25, 2026

Sodium hydride → 2,6-Dichloro-9-((2-(trimethylsilyl)ethoxy)methyl)-9H-purine

https://huagongshe.com/reaction/1453578

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant2-Chloromethyl 2-(trimethylsilyl)ethyl etherHCID 2724271—
Reactant2,6-DichloropurineHCID 5324412—
SolventDimethylformamideHCID 6228—
Product2,6-Dichloro-9-((2-(trimethylsilyl)ethoxy)methyl)-9H-purineHCID 58285232—

Reaction Steps

945 mg of 2,6-dichloropurine, 15 ml of DMF (dimethylformamide) and 288 mg of NaH are mixed and left at ambient temperature for 2 hours. 1.06 ml of 2-chloromethoxyethyltrimethylsilane are then added. The mixture is stirred for 18 hours at ambient temperature. The DMF is evaporated off. The product is taken up in methylene chloride. Washing is carried out with a saturated sodium bicarbonate solution and then once with H2O and, finally, with a saturated NaCl solution. Drying over Na2SO4 and evaporation to dryness are carried out. Purification is carried out by chromatography on silica with a CHCl3-AcOEt: 5-5 mixture for eluent. 876 mg of expected product are obtained, in the form of a yellow-colored oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07476670B2
Source datasetuspto-grants-2009_01
ORD IDord-9dae688878cc4cd98e06386b3760b190
Source noteuspto-grants-2009_01