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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1007682Generated: October 29, 2026

Homoveratrylamine → 1-Cyclohexyl-N-[2-(3,4-dimethoxyphenyl)ethyl]-2-(2-pyridinyl)-1H-benzimidazole-5-carboxamide

https://huagongshe.com/reaction/1007682

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHomoveratrylamineHCID 8421—
ReactantSodium HydroxideHCID 14798—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 491114HCID 491114—
ReactantO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
SolventDimethylformamideHCID 6228—
Product1-Cyclohexyl-N-[2-(3,4-dimethoxyphenyl)ethyl]-2-(2-pyridinyl)-1H-benzimidazole-5-carboxamideHCID 51389160%

Reaction Steps

1-Cyclohexyl-2-pyridin-2-yl-1H-benzoimidazole-5-carboxylic acid (0.060 g, 0.19 mmol), 3,4-dimethoxyphenethylamine (35 μL, 0.21 mmol) and TBTU (0.090 g, 0.28 mmol) were dissolved in DMF (1 mL), and DIEA (330 μL, 1.9 mmol) was added. The mixture was stirred 1 h at room temperature, when HPLC analysis indicated completion of the coupling reaction. The reaction mixture was added drop-wise with vigorous stirring to 1 N NaOH (10 mL). The precipitated product was collected by filtration, washed with water and dried. The title amide derivative was obtained as a gray solid (0.056 g, 60% yield, 98% homogeneity by HPLC).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06794404B2
Source datasetuspto-grants-2004_09
ORD IDord-5beb34dc4f1449d8a4c55f17fd2a3749
Source noteuspto-grants-2004_09