[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]=1A 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%)
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