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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 398797Generated: October 25, 2026

Hydrochloric Acid → 1-[5-(Undecylamino)hexyl]-3,7-dimethylxanthine

https://huagongshe.com/reaction/398797

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAmmonium HydroxideHCID 14923—
ReactantAmmonium ChlorideHCID 25517—
ReactantUndecylamineHCID 81742—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant1-(6-Oxohexyl)-3,7-dimethylxanthineHCID 18691065—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
Product1-[5-(Undecylamino)hexyl]-3,7-dimethylxanthineHCID 5388079087.6%

Reaction Steps

Sodium cyanoborohydride (63 mg, 1.0 mmol) was added to a mixture of 1-(6-oxohexyl)-3,7-dimethylxanthine (150 mg, 0.5 mmol), undecylamine (0.43 mL, 2.5 mmol), 38% aqueous hydrochloric acid solution (0.2 mL, 2.5 mmol), methanol (5 mL), and tetrahydrofuran (5 mL). The resulting mixture was stirred for 48 hours. Saturated aqueous ammonium chloride solution (20 mL) was added to the stirred mixture, followed by an additional 20 minutes of stirring and addition of 30% aqueous ammonium hydroxide solution (30 mL). The mixture was extracted with 25% methanol-dichloromethane (3×35 mL) and the combined extracts dried over sodium sulfate. The solvents were evaporated under vacuum, resulting in 190 mg of 1-[5-(Undecylamino)hexyl]-3,7-dimethylxanthine (86% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05817662
Source datasetuspto-grants-1998_10
ORD IDord-3fe3d023f4404ad58c652c80913c005e
Source noteuspto-grants-1998_10