Sodium hydride → (R)-1-(5-acetoxyhexyl)-3-(5-cyanopentyl)-7-methylxanthine

反応式

[C:1]([CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][N:8]1[C:16]2[N:15]=[CH:14][N:13]([CH3:17])[C:12]=2[C:11](=[O:18])[NH:10][C:9]1=[O:19])#[N:2].[H-].[Na+].[C:22]([O:25][C@H:26]([CH3:32])[CH2:27][CH2:28][CH2:29][CH2:30]I)(=[O:24])[CH3:23]>CS(C)=O>[C:22]([O:25][C@H:26]([CH3:32])[CH2:27][CH2:28][CH2:29][CH2:30][N:10]1[C:11](=[O:18])[C:12]2[N:13]([CH3:17])[CH:14]=[N:15][C:16]=2[N:8]([CH2:7][CH2:6][CH2:5][CH2:4][CH2:3][C:1]#[N:2])[C:9]1=[O:19])(=[O:24])[CH3:23]

参加物

実験手順

To a stirring solution of 0.31 g 3-(cyanopentyl)-7-methylxanthine (1.2 mmol) in 20 ml dimethyl sulfoxide was added 30 mg sodium hydride (1.3 mmol). After 25 minutes, 0.34 g of (R)-5-acetoxy-1-iodohexane (1.3 mol) was added and the mixture was stirred for 24 h. The mixture was then quenched with 70 ml water and extracted three times with 30 ml ethyl acetate. The combined extracts were washed two times with 35 ml saturated aqueous sodium chloride solution and dried over sodium sulfate, and concentrated under vacuum. The residue was purified by flash chromatography (silica gel) eluting with 5% methanol-ethyl acetate to give 0.42 g (R)-1-(5-acetoxyhexyl)-3-(5-cyanopentyl)-7-methylxanthine (88% yield) as a viscous oil.