HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 430706Generated: October 30, 2026
Hydrochloric Acid → 17-Allyl-3,14beta-dihydroxy-4,5alpha-epoxy-6beta-methylaminomorphinan
https://huagongshe.com/reaction/430706
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | Naloxone Hydrochloride | HCID 5464092 | — |
| Reactant | Methylamine hydrochloride | HCID 6364545 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 17-Allyl-3,14beta-dihydroxy-4,5alpha-epoxy-6beta-methylaminomorphinan | HCID 54248242 | 24% |
| Product | 17-Allyl-3,14beta-dihydroxy-4,5alpha-epoxy-6alpha-methylaminomorphinan | HCID 54248243 | 12% |
Reaction Steps
Naloxone hydrochloride (3.0 g), methylamine hydrochloride (5.57 g) and sodium cyanoborohydride (0.33 g) were suspended in anhydrous methanol (40 ml) and stirred for 17 hours at room temperature. After addition of concentrated hydrochloric acid (1.0 ml) and removal of solvent by distillation, distilled water (50 ml) was added followed by washing with chloroform (20 ml). Saturated aqueous sodium bicarbonate (10 ml) was added to make the solution basic followed by extraction with chloroform (30 ml×3). After drying with anhydrous magnesium sulfate, the solvent was distilled off. The resulting crude product was purified with silica gel column chromatography (Merk 7734 100 g; ethyl acetate/methanol/aqueous ammonia=90/10/1->80/20/2) to obtain the target compound in the form of a pure fraction (12 0.4 g, 12%; 13 0.8 g, 24%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06323212B1 |
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| Source dataset | uspto-grants-2001_11 |
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| ORD ID | ord-497a86575f1a4d57a396c41a34163baf |
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| Source note | uspto-grants-2001_11 |
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