Water → Naloxone 3-methyl ether
Reaction equation
[CH2:1]=[CH:2][CH2:3][N:4]1[C@@H:21]2[CH2:22][C:9]3[CH:10]=[CH:11][C:12]([OH:24])=[C:13]4[O:14][C@H:15]5[C:16]([CH2:18][CH2:19][C@:20]2([OH:23])[C@:7]5([C:8]=34)[CH2:6][CH2:5]1)=[O:17].[C:25]([O-])([O-])=O.[K+].[K+].CI.O>CN(C=O)C.C(Cl)Cl>[CH2:3]([N:4]1[CH2:5][CH2:6][C@@:7]23[C:8]4[C:9]5[CH2:22][C@@H:21]1[C@:20]2([OH:23])[CH2:19][CH2:18][C:16](=[O:17])[C@@H:15]3[O:14][C:13]=4[C:12]([O:24][CH3:25])=[CH:11][CH:10]=5)[CH:2]=[CH2:1]Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 2
Procedure
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).
Workup
- additionwas added dropwise via an addition funnel
- customa white precipitate formed
- filtrationthen filtered
- customto give a white solid
- washwashed with 1 N NaOH (400 mL)
- customThe layers were separated
- concentrationthe organic layer was concentrated
- customto give a wet solid
- filtrationthe solid was subsequently filtered
- customdried overnight in a vacuum oven
Sources & evidence
- ORD record
- ord-110e65a92c9c45eb8ab8929580c3c5e4
- Source dataset
- uspto-grants-2015_02
- Patent number
- US08946255B2
Reaction notes
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