HuagongsheHuagongshe Chemistry Print Report · For research reference only
Homoveratrylamine → 1-Cyclohexyl-N-[2-(3,4-dimethoxyphenyl)ethyl]-2-(2-pyridinyl)-1H-benzimidazole-5-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Homoveratrylamine | HCID 8421 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 491114 | HCID 491114 | — |
| Reactant | O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate | HCID 2733207 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-Cyclohexyl-N-[2-(3,4-dimethoxyphenyl)ethyl]-2-(2-pyridinyl)-1H-benzimidazole-5-carboxamide | HCID 513891 | 60% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06794404B2 |
| Source dataset | uspto-grants-2004_09 |
| ORD ID | ord-5beb34dc4f1449d8a4c55f17fd2a3749 |
| Source note | uspto-grants-2004_09 |