戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 127407作成日:2026年10月26日

1-Methylpyrrolidine-2-methylamine → N-(1-methyl-2-pyrrolidylmethyl)-1,4-benzodioxane-5-carboxamide

https://huagongshe.com/reaction/127407

反応式

関与物質

役割名称HCID仕込み量
反応物1-Methylpyrrolidine-2-methylamineHCID 117300—
反応物Methyl-7-methylsulfamoyl-1,4-benzodioxane-5-carboxylateHCID 54343297—
溶媒Acetic AcidHCID 176—
溶媒WaterHCID 962—
生成物N-(1-methyl-2-pyrrolidylmethyl)-1,4-benzodioxane-5-carboxamideHCID 53775438112%

反応手順

169 g of methyl-7-methylsulfamoyl-1,4-benzodioxane-5-carboxylate, 53 ml of water and 81 g of 1-methyl-2-aminomethylpyrrolidine were introduced into a balloon flask provided with a reflux condenser. The mixture was heated on a water bath until a test sample was totally soluble in dilute acids. The resulting crystals were dissolved in a solution of 50 ml of acetic acid in 1,250 ml of water and then the solution was filtered over carbon black and the base was reprecipitated by the addition of 100 ml of 20% ammonia. The crystals were dried off, washed with water and dried. 182 g of N-(1-methyl-2-pyrrolidylmethyl)-1,4-benzodioxane-5-carboxamide was produced (M.P.: 189°-190° C.; yield: 83.6%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04255580
出典データセットuspto-grants-1981_03
ORD IDord-52d36f660dca4f7a94c7961311a582bd
出典メモuspto-grants-1981_03