戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 5069作成日:2026年10月26日

Methyl iodide → (2S, 4S)-2-Carbamoyl-4-(3-methoxybenzylthio)-1-methylpyrrolidine

https://huagongshe.com/reaction/5069

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl iodideHCID 6328—
反応物Sodium BicarbonateHCID 516892—
反応物(2S, 4S)-2-Carbamoyl-4-(4-methoxybenzylthio)-pyrrolidineHCID 14880267—
溶媒DimethylformamideHCID 6228—
生成物(2S, 4S)-2-Carbamoyl-4-(3-methoxybenzylthio)-1-methylpyrrolidineHCID 56983387—

反応手順

0.07 ml of methyl iodide was added, whilst ice-cooling, to a solution of 0.6 g of (2S, 4S)-2-carbamoyl-4-(4-methoxybenzylthio)pyrrolidine [prepared as described in step (5) above] dissolved in 4.5 ml of dry dimethylformamide. The mixture was then stirred at 0° to 5° C. for 5 minutes and at room temperature for 20 minutes. At the end of this time, the reaction mixture was poured into a saturated aqueous solution of sodium bicarbonate and then extracted with ethyl acetate. The extract was washed with an aqueous solution of sodium chloride and dried over anhydrous magnesium sulfate. The solvent was removed by distillation under reduced pressure, and then the residue was subjected to column chromatography using a Lobar column (Merck, LiChroprep Si 60, size B), and 252 mg of the title compound, melting at 113°-114° C., were obtained as crystals from the fractions eluted with a 9:1 by volume mixture of ethyl acetate and methanol.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05242914
出典データセットuspto-grants-1993_09
ORD IDord-744e3ebab8024cf1ac0a111f766472de
出典メモuspto-grants-1993_09