[H-].[Na+].[Cl:3][C:4]1[C:9]([NH:10][S:11]([CH3:14])(=[O:13])=[O:12])=[CH:8][C:7]([N:15]2[C:20](=[O:21])[CH:19]=[C:18]([C:22]([F:25])([F:24])[F:23])[N:17]([CH3:26])[C:16]2=[O:27])=[C:6]([F:28])[CH:5]=1.[CH3:29][S:30](Cl)(=[O:32])=[O:31]>O1CCCC1>[Cl:3][C:4]1[C:9]([N:10]([S:30]([CH3:29])(=[O:32])=[O:31])[S:11]([CH3:14])(=[O:13])=[O:12])=[CH:8][C:7]([N:15]2[C:20](=[O:21])[CH:19]=[C:18]([C:22]([F:25])([F:24])[F:23])[N:17]([CH3:26])[C:16]2=[O:27])=[C:6]([F:28])[CH:5]=1To a suspension of 0.05g of sodium hydride(purity:60%) and 5 ml of tetrahydrofuran, 0.5g of 3-(4-chloro-2-fluoro-5-methanesulfonylaminophenyl)-1-methyl-6-trifluoromethyl-2,4(1H, 3H)-pyrimidinedione was added at a temperature of 0° C. Then 0.11 ml of methanesulfonyl chloride was added dropwise to the resultant suspension. After stirring for 7 hburs, the reaction mixture was poured into ice water and extracted with ethyl acetate. The extract of the ethyl acetate layer was washed with a saturated sodium chloride agueous solution and dried over anhydrous sodium sulfate. Then ethyl acetate was distilled off to obtain a crude product. The obtained product was washed with diethyl ether to obtain 0.50g of the objective product as white crystals.
Wird geladen…