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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1943834Generated: October 25, 2026

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

https://huagongshe.com/reaction/1943834

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 numberUS08394808B2
Source datasetuspto-grants-2013_03
ORD IDord-61bea09302c246549c77ace1e119f222
Source noteuspto-grants-2013_03