Methyl iodide → 7-(5-Chloro-2-methoxyphenyl)-8-hydroxymethyl-1,3,3-trimethyl-3,4-dihydro-1H-quinoxalin-2-one

HRID 871975Notes

Reaction equation

[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([OH:24])=[C:6]([C:8]2[CH:17]=[C:16]3[C:11]([N:12](CO)[C:13]([CH3:21])([CH3:20])[C:14](=[O:19])[N:15]3[CH3:18])=[CH:10][CH:9]=2)[CH:7]=1.CI.[C:27](=[O:30])([O-])[O-].[K+].[K+].[C:33](OCC)(=O)C>CN(C)C=O.O.C(OCC)C>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([O:24][CH3:33])=[C:6]([C:8]2[C:17]([CH2:27][OH:30])=[C:16]3[C:11]([NH:12][C:13]([CH3:21])([CH3:20])[C:14](=[O:19])[N:15]3[CH3:18])=[CH:10][CH:9]=2)[CH:7]=1

Participants

Conditions

Temperature: 50 °C

Procedure

A mixture of 7-(5-chloro-2-hydroxyphenyl)-hydroxymethyl-1,3,3-trimethyl-3,4-dihydro-1H-quinoxalin-2-one (Reference Compound No. 12-1, 1.36 g, 3.92 mmol), methyl iodide (244 μL, 3.92 mmol), and potassium carbonate (1.08 g, 7.81 mmol) was suspended in anhydrous N,N-dimethylformamide (20 mL) and stirred at 50° C. for 1 hour. After cooling down, ethyl acetate (70 mL), diethylether (70 mL), and water (150 mL) were added and partitioned. The organic layer was washed with water (100 mL) and saturated brine (50 mL) successively, dried over anhydrous magnesium sulfate, and then the solvent was removed under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane-ethyl acetate) to give the titled reference compound (1.36 g) as a pale yellow amorphous product. (Yield 96%)

Workup

temperatureAfter cooling down
custompartitioned
washThe organic layer was washed with water (100 mL) and saturated brine (50 mL) successively
dry with materialdried over anhydrous magnesium sulfate
customthe solvent was removed under reduced pressure
customThe obtained residue was purified by silica gel column chromatography (hexane-ethyl acetate)

Sources & evidence

ORD record: ord-7c888f394da64d22961bdf8a42e680d2
Source dataset: uspto-grants-2015_03
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US08975256B2

Reaction notes

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