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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2181620Generated: November 1, 2026

Potassium Carbonate → HCID 10151688, compound

https://huagongshe.com/reaction/2181620

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantBenzyl chloromethyl etherHCID 137983—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 11772127HCID 11772127—
CatalystTetrabutylammonium IodideHCID 67553—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
ProductHCID 10151688HCID 1015168865%

Reaction Conditions

Temperature45 °C

Reaction Steps

3-(2,4-dichlorophenyl)-8-ethyl-1-methyl-3,7-dihydro-1H-purine-2,6-dione (6.00 g, 17.69 mmol), prepared according to the procedure in example 1, was dissolved in anhydrous DMF (80 mL). K2CO3 (6.11 g, 44.23 mmol), Bu4NI (1.31 g, 3.54 mmol) and BOMCl (4.4 mL, 31.84 mmol) were added and the reaction mixture was heated at 45° C. for 50 min. The reaction mixture was cooled to rt and was stirred with saturated aqueous NaHCO3 (180 mL) for 30 min. The mixture was poured into a separatory funnel containing ether (600 mL). The organic layer was washed with H2O (4×80 mL), brine, dried over MgSO4, filtered, and concentrated. The residue was purified by column chromatography on silica gel (40% ethyl acetate in hexanes) to give 7-benzyloxymethyl-3-(2,4-dichlorophenyl)-8-ethyl-1-methyl-3,7-dihydro-1H-purine-2,6-dione (5.28 g, 65% yield) as an amorphous solid: 1H NMR (300 MHz, CDCl3) δ 7.59 (d, J=2.2 Hz, 1H), 7.42 (dd, J=8.4, 2.2 Hz, 1H), 7.37-7.26 (m, 6H), 5.86 (ABq, JAB=11.0, Δυ=39.7 Hz, 2H), 4.72 (s, 2H), 3.46 (s, 3H), 2.79 (q, J=7.7 Hz, 2H), 1.25 (t, J=7.6 Hz, 3H); LRMS (APCI) m/e 459.0 [(M+H)+, calcd for C22H21N4O3Cl2 459.1].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06894045B2
Source datasetuspto-grants-2005_05
ORD IDord-4f43af065a8040ce9acccb6125f991ba
Source noteuspto-grants-2005_05