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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 32287Generated: October 26, 2026

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/reaction/32287

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Amino-N-[2-(diethylamino)ethyl]-2-methoxybenzamideHCID 77374—
Reactant1,3-Benzodioxole-5-carbonyl chlorideHCID 2734749—
SolventChloroformHCID 6212—
ProductBenzo[1,3]-dioxole-5-carboxylic acid [4-(2-diethylamino-ethylcarbarnoyl)-5-methoxy-phenyl]-amideHCID 5979334167%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07427390B2
Source datasetuspto-grants-2008_09
ORD IDord-edf55ea1959844a7beb69242da746a76
Source noteuspto-grants-2008_09