Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Naloxone | HCID 5284596 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Naloxone 3-methyl ether | HCID 11056967 | 66% |
Reaction Steps
To a solution of naloxone (50 g, 125 mmol) in 50 mL of DMF was added K2CO3 (51.8 g, 375 mmol). The resulting suspension was stirred at ambient temperature for 30 min whereupon methyl iodide (7.82 mL, 125 mmol) in 7 mL of DMF was added dropwise via an addition funnel. The suspension was maintained overnight at ambient temperature. The reaction mixture was added to 1 L of H2O and a white precipitate formed. The mixture was stirred for 1 h then filtered to give a white solid. The solid was dissolved in CH2Cl2 (700 mL) and washed with 1 N NaOH (400 mL). The layers were separated and the organic layer was concentrated, to give a wet solid. Water was added and the solid was subsequently filtered and dried overnight in a vacuum oven to afford 28.1 g (66%) of Compound 2 as a white solid. LC/MS, m/z 342.2 [M+H]+ (Calc: 342.40).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08946255B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-110e65a92c9c45eb8ab8929580c3c5e4 |
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| Source note | uspto-grants-2015_02 |
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