Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 14-Hydroxymorphine-6-one | HCID 15286253 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | N-methylpyrrolidone-water | HCID 22287110 | — |
| Product | Naloxone | HCID 5284596 | 84.3% |
Reaction Steps
Allyl bromide (56 mg; 0.463 mmol) and Et3N (45 μl; 0.327 mmol) were added to a suspension of noroxymorphone (Example 5, 100 mg; 0.348 mmol) in a mixture of NMP/H2O (10:1; 0.35 mL). The reaction vessel was purged with argon and the mixture was stirred at 70° C. for 2 h. At that time, additional Et3N (45 μl; 0.327 mmol) was added and the mixture was stirred for an additional 7.5 h at 70° C. The reaction mixture was then cooled to room temperature, diluted with dichloromethane (15 mL), and washed with saturated NaHCO3 (3×3 mL). The aqueous layer was re-extracted with dichloromethane (5 mL) and the combined organic layers were dried over MgSO4. Column chromatography of the residue (dichloromethane/methanol 4:1) afforded 96 mg (84%) of naloxone as a white solid mp: 181-182° C. (ethyl acetate), [lit. mp 173-175]xix [lit. 179.5° C. (toluene)]xx identical in all respects to the material described in the literature.xxi
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09045497B1 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-29adc877c2fa4e2e867f1204b482daa4 |
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| Source note | uspto-grants-2015_06 |
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