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Benzenesulfonyl isocyanate, 2-chloro- → N-(2-chlorophenylsulfonyl)-N'-(1,2,4-triazol-1-ylmethyl)-N'-(4,6-dimethylpyrimidin-2-yl)urea
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-dimethylpyrimidine | HCID 23043237 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 生成物 | N-(2-chlorophenylsulfonyl)-N'-(1,2,4-triazol-1-ylmethyl)-N'-(4,6-dimethylpyrimidin-2-yl)urea | HCID 23043228 | 62.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04764203 |
| 出典データセット | uspto-grants-1988_08 |
| ORD ID | ord-2a190885aa844be6a5c9bf66613d2532 |
| 出典メモ | uspto-grants-1988_08 |