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HRID 127403作成日:2026年10月26日

Acetate → N-(1-allyl-2-pyrrolidylmethyl)-7-sulfamoyl-1,4-benzodioxane-5-carboxamide

https://huagongshe.com/reaction/127403

反応式

関与物質

役割名称HCID仕込み量
反応物AcetateHCID 175—
反応物1-(Allyl)pyrrolidine-2-methylamineHCID 117296—
反応物Methyl-7-sulfamoyl-1,4-benzodioxane-5-carboxylateHCID 20544687—
溶媒WaterHCID 962—
生成物N-(1-allyl-2-pyrrolidylmethyl)-7-sulfamoyl-1,4-benzodioxane-5-carboxamideHCID 2483492764.8%

反応手順

145 g of methyl-7-sulfamoyl-1,4-benzodioxane-5-carboxylate, 48 g of water and 89 g of 1-allyl-2-aminomethyl-pyrrolidine were introduced into a balloon flask provided with a condenser. The mixture was heated on a water bath until a test sample was soluble in dilute acids and then 1 liter of water was added. The precipitated carboxamide was redissolved by acetate formation. The solution formed was filtered on carbon black and then the base was precipitated by the addition of 20% ammonia. The resulting crystals were dried off, washed with water, dried and purified by passing over hydrochloride (M.P.: 228°-230° C.) followed by transformation into a base by treatment with 20% ammonia. 131 g of N-(1-allyl-2-pyrrolidylmethyl)-7-sulfamoyl-1,4-benzodioxane-5-carboxamide was produced (M.P.: 143°-144° C.; yield: 64.8%). The structure was confirmed by nuclear magnetic resonance.

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-d432ac23ca704fcdb426b3353b672908
出典メモuspto-grants-1981_03