Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1880052Generated: October 27, 2026

Triethylamine → (4-benzyloxy-phenyl)-(1-methyl-1H-benzoimidazol-2-yl)-amine

https://huagongshe.com/reaction/1880052

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant4-BenzyloxyanilineHCID 22860—
ReactantN-Methyl-o-phenylenediamineHCID 78498—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
Product(4-benzyloxy-phenyl)-(1-methyl-1H-benzoimidazol-2-yl)-amineHCID 59327107—

Reaction Steps

To a solution of 4-benzyloxy-phenylamine (2 g, 8.4 mmol) in 30 mL of DCM was added triethylamine (1 mL) and di-2-pyridylthionocarbonate (2.5 g, 8.4 mmol). The resulting mixture was stirred at RT for 2 h. The reaction mixture was diluted with DCM and washed with water and brine. The organic layer was then dried over Na2SO4, filtered and concentrated. The residue was dissolved in 30 mL DMF, N-methyl-benzene-1,2-diamine (1.5 g, 12.7 mmol) and EDCI (2 g, 10.5 mmol). The resulting mixture was heated at 70° C. for 4 h. The reaction was cooled to RT, diluted with ethyl acetate and washed with water and brine. Purification by silica gel chromatography (98:2 chlorforma/MeOH) afforded the desired product (4-benzyloxy-phenyl)-(1-methyl-1H-benzoimidazol-2-yl)-amine. [M+1]=330.1

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08318718B2
Source datasetuspto-grants-2012_11
ORD IDord-34bd763df4dc489d8b4c8edd8c7cedab
Source noteuspto-grants-2012_11