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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 929189Generated: November 1, 2026

Ethyl Acetate → 2-chloro-8-(methylsulfonyl)-7-((2-(trimethylsilyl)ethoxy)methyl)-7H-purine

https://huagongshe.com/reaction/929189

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantDiisopropylethylamineHCID 81531—
Reactant2-Chloromethyl 2-(trimethylsilyl)ethyl etherHCID 2724271—
Reactant2-chloro-8-(methylsulfonyl)-7H-purineHCID 90041840—
SolventDimethylformamideHCID 6228—
Product2-chloro-8-(methylsulfonyl)-7-((2-(trimethylsilyl)ethoxy)methyl)-7H-purineHCID 90042499—

Reaction Steps

To a stirring solution of 2-chloro-8-(methylsulfonyl)-7H-purine (570 mg, 2.45 mmol) and N,N-diisopropylethylamine (3.42 mL, 19.60 mmol) in anhydrous DMF (16.7 mL) was added 2-(trimethylsilyl)ethoxymethyl chloride (2.17 mL, 12.25 mmol). The reaction was stirred under N2 at RT for 20 h, then added to EtOAc (1.0 L) and washed with saturated NH4Cl (0.2 L). The aqueous layer was separated and back-extracted with EtOAc (0.2 L). The organic layers combined and evaporated under reduced pressure. Flash chromatography of the resulting residue utilizing a 24 g silica RediSep Rf® Gold column and employing a 0-40% EtOAc/hexane gradient afforded the title compound. LC-MS: calculated for C12H19ClN4O3SSi 362.06 observed m/e: 385.30 (M+23)′ (Rt 1.33/2.0 min)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09290517B2
Source datasetuspto-grants-2016_03
ORD IDord-6abdc0f627f740abaf8547fe576d7159
Source noteuspto-grants-2016_03