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Sodium hydride → 1-(2-Chloro-5-pyridylmethyl)-2-[(4-chlorophenylthio)nitromethylene]imidazolidine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Sodium hydride | HCID 24758 | — |
| 反応物 | 2-Chloro-5-{[2-(nitromethylidene)imidazolidin-1-yl]methyl}pyridine | HCID 180957 | — |
| 反応物 | 4-Chlorobenzenesulfenylchloride | HCID 11084465 | — |
| 反応物 | HCID 178418361 | HCID 178418361 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 1-(2-Chloro-5-pyridylmethyl)-2-[(4-chlorophenylthio)nitromethylene]imidazolidine | HCID 86742144 | — |
反応手順
0.2 g of sodium hydride 60% in oil was added to a solution of 1.3 g of 1-(2-chloro-5-pyridylmethyl)-2-nitromethyleneimidazolidine in 15 ml of dry dimethylformamide, and the mixture was stirred at room temperature until the generation of hydrogen gas ceased. 0.9 g of 4-chlorobenzenesulfenylchloride was then drop into the solution at 0° C. with stirring. After stirring for 1 hour at room temperature, the reaction mixture was poured into ice water. The precipitated crystal was filtered and recrystalized from ethyl acetate to give 1-(2-chloro-5-pyridylmethyl)-2-{(4chlorophenylthio)nitromethylene}imidazolidine. The yield was 1.3 g.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05001138 |
| 出典データセット | uspto-grants-1991_03 |
| ORD ID | ord-87869d9c9f384815ba37abdf0afa835d |
| 出典メモ | uspto-grants-1991_03 |