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HRID 359513作成日:2026年10月24日

Sodium hydride → 1-(2-Chloro-5-pyridylmethyl)-2-[(4-chlorophenylthio)nitromethylene]imidazolidine

https://huagongshe.com/ja/reaction/359513

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium hydrideHCID 24758—
反応物2-Chloro-5-{[2-(nitromethylidene)imidazolidin-1-yl]methyl}pyridineHCID 180957—
反応物4-ChlorobenzenesulfenylchlorideHCID 11084465—
反応物HCID 178418361HCID 178418361—
溶媒DimethylformamideHCID 6228—
生成物1-(2-Chloro-5-pyridylmethyl)-2-[(4-chlorophenylthio)nitromethylene]imidazolidineHCID 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

DOI10.6084/m9.figshare.5104873.v1
特許番号US05001138
出典データセットuspto-grants-1991_03
ORD IDord-87869d9c9f384815ba37abdf0afa835d
出典メモuspto-grants-1991_03