戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1154697作成日:2026年10月27日

Dimethylamine → 6-Dimethylaminomethyl-2-[(2-phthalimidoethyl)thiomethyl]pyridine

https://huagongshe.com/reaction/1154697

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylamineHCID 674—
反応物2-PhthalimidoethanethiolHCID 96248—
反応物2,6-Bis(chloromethyl)pyridineHCID 316654—
反応物Sodium MethoxideHCID 10942334—
溶媒MethanolHCID 887—
溶媒DichloromethaneHCID 6344—
生成物6-Dimethylaminomethyl-2-[(2-phthalimidoethyl)thiomethyl]pyridineHCID 20434281—

反応手順

To a solution of N-(2-mercaptoethyl) phthalimide (28.8 g, 0.139 mol) in dry methanol (250 ml) is added sodium methoxide (7.5 g, 0.139 mol) with cooling and stirring. This mercaptide solution is added to 2,6-bis(chloromethyl)pyridine (24.5 g, 0.139 mol) in dry methanol (250 ml). The mixture is stirred at room temperature for 21/2 hours and is filtered to remove the precipitated solid. Then dimethylamine (6.9 g, 0.153 mol) in cold methanol (150 ml) is added to the filtrate and the mixture is stirred at room temperature overnight. The solvent is removed in vacuo leaving an amber gum. The gum is taken up in methylene chloride (200 ml) and is washed with aqueous sodium bicarbonate and with water. The methylene chloride layer is dried over anhydrous sodium sulfate, filtered and concentrated in vacuo. This gives 24.3 g of 6-dimethylaminomethyl-2-[(2-phthalimidoethyl)thiomethyl]pyridine as a crude amber gum.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04490533
出典データセットuspto-grants-1984_12
ORD IDord-68ae5f5889ee49be83fb4a3600db0820
出典メモuspto-grants-1984_12