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HRID 34868作成日:2026年10月23日

Benzenesulfonyl isocyanate, 2-chloro- → N-(2-chlorophenylsulfonyl)-N'-(1,2,4-triazol-1-ylmethyl)-N'-(4,6-dimethylpyrimidin-2-yl)urea

https://huagongshe.com/ja/reaction/34868

反応式

関与物質

役割名称HCID仕込み量
反応物Benzenesulfonyl isocyanate, 2-chloro-HCID 174071—
反応物2-(1,2,4-Triazol-1-ylmethylamino)-4,6-dimethylpyrimidineHCID 23043237—
溶媒AcetonitrileHCID 6342—
生成物N-(2-chlorophenylsulfonyl)-N'-(1,2,4-triazol-1-ylmethyl)-N'-(4,6-dimethylpyrimidin-2-yl)ureaHCID 2304322862.4%

反応手順

4 g (0.019 mole) of 2-(1,2,4-triazol-1-ylmethylamino)-4,6-dimethylpyrimidine are suspended in 100 ml of absolute acetonitrile and then 4.3 g (0.019 mole) of 2-chlorophenylsulfonylisocyanate are stirred into the suspension. The batch is stirred for 24 hours at room temperature and the resultant solution is finally concentrated in a rotary evaporator. Crystals of the title compound precipitate and are recrystallised from ethyl acetate, affording 5 g (62% of theory) of the above urea, which melts at 152°-157° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04764203
出典データセットuspto-grants-1988_08
ORD IDord-2a190885aa844be6a5c9bf66613d2532
出典メモuspto-grants-1988_08