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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 60348Generated: October 29, 2026

1-Chloro-4-(chloromethyl)benzene → HCID 118863766, compound

https://huagongshe.com/reaction/60348

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Chloro-4-(chloromethyl)benzeneHCID 7723—
ReactantPotassium CarbonateHCID 11430—
Reactant3-(6-(3-chlorophenyl)-1-methyl-2,4-dioxo-1H-pyrrolo[3,2-d]pyrimidin-3(2H,4H,5H)-yl)propylacetateHCID 118863772—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 118863766HCID 11886376650%

Reaction Conditions

Temperature85 °C

Reaction Steps

To a mixture of 3-(6-(3-chlorophenyl)-1-methyl-2,4-dioxo-1H-pyrrolo[3,2-d]pyrimidin-3(2H,4H,5H)-yl)propyl acetate (60 mg, 0.16 mmol), K2CO3 (110 mg, 0.80 mmol) in DMF (2 ml) was added 1-chloro-4-(chloromethyl)benzene (51 mg, 0.32 mmol). The reaction was heated at 85° C. for 2 h, cooled to RT then diluted with EA (20 mL) and water (20 mL). The organic layer was dried over Na2SO4 and concentrated to give 3-(5-(4-chlorobenzyl)-6-(3-chlorophenyl)-1-methyl-2,4-dioxo-1H-pyrrolo[3,2-d]pyrimidin-3(2H,4H,5H)-yl)propyl acetate (40 mg, 50% yield) as an oil. LCMS: MH+ 500 and TR=1.847 min. Used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09440983B2
Source datasetuspto-grants-2016_09
ORD IDord-cfae0f83fee3441ea6a33907f0460a15
Source noteuspto-grants-2016_09