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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 32287생성일: 2026년 10월 24일

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/ko/reaction/32287

반응식

참여 물질

역할이름HCID투입량
반응물4-Amino-N-[2-(diethylamino)ethyl]-2-methoxybenzamideHCID 77374—
반응물1,3-Benzodioxole-5-carbonyl chlorideHCID 2734749—
용매ChloroformHCID 6212—
생성물Benzo[1,3]-dioxole-5-carboxylic acid [4-(2-diethylamino-ethylcarbarnoyl)-5-methoxy-phenyl]-amideHCID 5979334167%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07427390B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-edf55ea1959844a7beb69242da746a76
출처 메모uspto-grants-2008_09