Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 535653Generated: October 25, 2026

Dimethylamine → 7-(4-benzylpiperazin-1-yl)-N,N-dimethylbenzofuran-2-carboxamide

https://huagongshe.com/reaction/535653

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylamineHCID 674—
Reactant1,4-Diazabicyclo(2.2.2)octane--trimethylalumane (1/2)HCID 16688366—
Reactant7-(4-Benzyl-piperazin-1-yl)-benzofuran-2-carboxylic acid ethyl esterHCID 59636745—
SolventTetrahydrofuranHCID 8028—
SolventSodium chloride; waterHCID 57417360—
Product7-(4-benzylpiperazin-1-yl)-N,N-dimethylbenzofuran-2-carboxamideHCID 5963677087.7%

Reaction Conditions

Temperature120 °C

Reaction Steps

7-(4-Benzyl-piperazin-1-yl)-benzofuran-2-carboxylic acid ethyl ester (1.0 g, 2.74 mmol) and DABAL-Me3 (0.56 g, 2.20 mmol) were mixed in tetrahydrofuran (5 mL). Dimethylamine (2M in THF) (2.2 mL, 4.39 mmol) was added and the mixture was heated by microwave irradiation to 120° C. for 15 min. Brine was added and the mixture was extracted with dichloromethane, dried over Na2SO4, filtered and the solvent removed by rotary evaporation. The product was purified by flash chromatography (SiO2; DCM/MeOH; gradient 0-2%) giving 7-(4-benzylpiperazin-1-yl)-N,N-dimethylbenzofuran-2-carboxamide (0.70 g, 1.93 mmol) in 70% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08859534B2
Source datasetuspto-grants-2014_10
ORD IDord-fad5ab25af9f4a149521755b80ec1b68
Source noteuspto-grants-2014_10