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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2386651Generated: October 25, 2026

Hydrochloric Acid → 8-Chloro-3-octyl-3,7-dihydro-1H-purine-2,6-dione

https://huagongshe.com/reaction/2386651

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMorpholineHCID 8083—
ReactantSodium CarbonateHCID 10340—
Reactant1-IodooctaneHCID 12380—
Reactant8-ChloroxanthineHCID 26103—
CatalystHCID 178418397HCID 178418397—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product8-Chloro-3-octyl-3,7-dihydro-1H-purine-2,6-dioneHCID 59299546—

Reaction Steps

8-Chloro-3,7-dihydro-1H-purine-2,6-dione (100 mg, 0.44 mmol) was stirred with sodium carbonate (52 mg, 0.49 mmol) in dry DMF (3 ml) for 20 min., then 1-iodooctane (118 mg, 0.49 mmol) was added and the mixture was stirred under nitrogen at 40 C for 65 h. After cooling to room temperature, the mixture was thoroughly degassed by evacuating the vessel and refilling with nitrogen several times. Tetrakis(triphenylphosphine)palladium(0) (102 mg, 0.09 mmol) was added, the mixture degassed again and then morpholine (0.385 ml, 4.4 mmol) added and stirring continued for 6.5 h. 2M HCl and EtOAc were added, and the 2-phase system was filtered. The product was present predominantly in the filtered solid, which was recrystallised from THF-acetonitrile, followed by MeOH, with filtration, to afford the pure title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08268839B2
Source datasetuspto-grants-2012_09
ORD IDord-485829e54dfc466bafcf0e4400abf024
Source noteuspto-grants-2012_09