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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1738793Generated: November 1, 2026

Hydrochloric Acid → 1-(6-Dibutylamino-3-hydroxy-3-methyl-4-hexynyl)-3-methyl-7-propyl-xanthine

https://huagongshe.com/reaction/1738793

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant3-Dibutylamino-1-propyneHCID 138732—
Reactant3-Methyl-1-(3-oxobutyl)-7-propylxanthineHCID 15390923—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product1-(6-Dibutylamino-3-hydroxy-3-methyl-4-hexynyl)-3-methyl-7-propyl-xanthineHCID 15390909—

Reaction Steps

6.73 ml (10.77 mmol) of a 15% strength butyllithium solution in n-hexane were slowly added dropwise to a solution of 2.09 ml (10.77 mmol) of N,N-dibutyl-2-propynylamine in 20 ml of tetrahydrofuran at -65° C. The mixture was stirred at -60° C. to -65° C. for one hour and warmed to room temperature, and a solution of 2.0 g (7.18 mmol) of 3-methyl-1-(3-oxobutyl)-7-propylxanthine in 30 ml of tetrahydrofuran was added. The slightly exothermic reaction was complete after 30 minutes. The mixture was adjusted to pH 5-6 with 1 N hydrochloric acid and partitioned between dichloromethane and water. The organic phase was washed with water, dried with magnesium sulfate and concentrated under reduced pressure. The oily crude product was purified by flash chromatography, dichloromethane/methanol =19/0.75.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05965555
Source datasetuspto-grants-1999_10
ORD IDord-ab80205827d045e28210f06af697e415
Source noteuspto-grants-1999_10