戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1441277作成日:2026年10月27日

Sodium Iodide → {5-[(2-Chloro-5-nitro-phenylamino)-methyl]-2-methylsulfanyl-pyrimidin-4-yl}-methyl-amine

https://huagongshe.com/reaction/1441277

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium IodideHCID 5238—
反応物2-Chloro-5-nitroanilineHCID 22691—
反応物(5-Chloromethyl-2-methylsulfanyl-pyrimidin-4-yl)-methyl-amine hydrochlorideHCID 21988143—
溶媒AcetonitrileHCID 6342—
生成物{5-[(2-Chloro-5-nitro-phenylamino)-methyl]-2-methylsulfanyl-pyrimidin-4-yl}-methyl-amineHCID 6870028897%

反応条件

温度0 °C

反応手順

15.85 g (5-Chloromethyl-2-methylsulfanyl-pyrimidin-4-yl)-methyl-amine hydrochloride, 1.979 g sodium iodide, and 34.49 mL N—N-diisopropylethylamine were solved in 150 ml acetonitrile and cooled to 0° C. 17.085 g 2-Chloro-5-nitrophenylamine dissolved in 150 ml acetonitrile were added slowly under stirring. The reaction mixture was stirred at room temperature for 48 hrs, then the solvent was evaporated. The residue was solved in a mixture of water/acetic acid ethyl ester (1:1), stirred and the crystalline product was sucked off and dried for 48 h under vacuum at 40° C. The two phases of the mother liquor were separated and the aqueous phase was extracted with dichloromethane. The organic phases were combined, dried over sodium sulfate, the solvent was evaporated and the residue was rubbed with diethyl ether. Both residues were combined and gave of the title product in 97% yield.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07655651B2
出典データセットuspto-grants-2010_02
ORD IDord-a7ffede59ec546858625a703cfd9251e
出典メモuspto-grants-2010_02