Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1419780Generated: October 25, 2026

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

https://huagongshe.com/reaction/1419780

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×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 numberUS05889011
Source datasetuspto-grants-1999_03
ORD IDord-1ffac374c5524058a407cf5d5fafef18
Source noteuspto-grants-1999_03