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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 383825Generated: October 26, 2026

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

https://huagongshe.com/reaction/383825

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; to 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 numberUS08367676B2
Source datasetuspto-grants-2013_02
ORD IDord-7ecdbf52ef48430799ea9f2a5d938b07
Source noteuspto-grants-2013_02