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HRID 981742作成日:2026年10月27日

N-[2-(N,N-dimethylsulfamoyl)-phenylsulfonyl]-N'-(4-chloromethyl-6-methoxypyrimidin-2-yl)-urea → N-(2-Dimethylsulfamoylphenyl-sulfonyl)-N'-(4-methoxy-6-dimethylthiocarbamoylthiomethyl-pyrimidin-2-yl)-urea

https://huagongshe.com/reaction/981742

反応式

関与物質

役割名称HCID仕込み量
反応物N-[2-(N,N-dimethylsulfamoyl)-phenylsulfonyl]-N'-(4-chloromethyl-6-methoxypyrimidin-2-yl)-ureaHCID 13884816—
反応物Sodium dimethyldithiocarbamate dihydrateHCID 23693613—
溶媒WaterHCID 962—
溶媒AcetonitrileHCID 6342—
生成物N-(2-Dimethylsulfamoylphenyl-sulfonyl)-N'-(4-methoxy-6-dimethylthiocarbamoylthiomethyl-pyrimidin-2-yl)-ureaHCID 20070845—

反応手順

A mixture of 9.3 g of N-(2-dimethylsulfamoylphenyl-sulfonyl)-N'-(4-chloromethyl-6-methoxy-pyrimidin-2-yl)urea and 3.7 g of dimethyldithiocarbamic acid sodium salt dihydrate is stirred in 100 ml of acetonitrile at 20°-25° C. for 3 hours. In further processing, the reaction mixture is diluted with 1 liter of water, and the precipitated product is separated. The yield is 10.0 g (91% of theory) of N-(2-dimethylsulfamoylphenyl-sulfonyl)-N'-(4-methoxy-6dimethylthiocarbamoylthiomethyl-pyrimidin-2-yl)-urea m.p. 181°14 183° C. (decomp.).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04992549
出典データセットuspto-grants-1991_02
ORD IDord-beced3524b984a13af0d3df3ea465759
出典メモuspto-grants-1991_02