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HRID 32287作成日:2026年10月24日

4-Amino-N-[2-(diethylamino)ethyl]-2-methoxybenzamide → Benzo[1,3]-dioxole-5-carboxylic acid [4-(2-diethylamino-ethylcarbarnoyl)-5-methoxy-phenyl]-amide

https://huagongshe.com/ja/reaction/32287

反応式

関与物質

役割名称HCID仕込み量
反応物4-Amino-N-[2-(diethylamino)ethyl]-2-methoxybenzamideHCID 77374—
反応物1,3-Benzodioxole-5-carbonyl chlorideHCID 2734749—
溶媒ChloroformHCID 6212—
生成物Benzo[1,3]-dioxole-5-carboxylic acid [4-(2-diethylamino-ethylcarbarnoyl)-5-methoxy-phenyl]-amideHCID 5979334167%

反応手順

200 mg (0.75 mmol) of 4-amino-N-(2-diethylamino-ethyl)-2-methoxy-benzamide in 10 ml of chloroform is mixed with 5 ml of 3,4-methylenedioxybenzoic acid chloride (in chloroform) and this mixture is stirred for 3 hours at room temperature. After concentration by evaporation in a vacuum, the residue is taken up in 40 ml of dilute sodium bicarbonate solution and then extracted with 40 ml of methylene chloride. The methylene chloride phase is washed with water, dried, filtered and concentrated by evaporation. The crude product, 315 mg, is taken up in methylene chloride and purified on silica gel. As a mobile solvent, a mixture that consists of methylene chloride/methanol (97:3→90:10) is used. 210 mg (67% of theory) of benzo[1,3]dioxole-5-carboxylic acid [4-(2-diethylamino-ethylcarbamoyl)-5-methoxy-phenyl]-amide (melting point 131.1° C.) is obtained.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07427390B2
出典データセットuspto-grants-2008_09
ORD IDord-edf55ea1959844a7beb69242da746a76
出典メモuspto-grants-2008_09