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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Undecylamine | HCID 81742 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | 1-(6-Oxohexyl)-3,7-dimethylxanthine | HCID 18691065 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 1-[5-(Undecylamino)hexyl]-3,7-dimethylxanthine | HCID 53880790 | 87.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05889011 |
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| Source dataset | uspto-grants-1999_03 |
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| ORD ID | ord-1ffac374c5524058a407cf5d5fafef18 |
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| Source note | uspto-grants-1999_03 |
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