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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide | HCID 15908 | — |
| Reactant | 4-Benzyloxyaniline | HCID 22860 | — |
| Reactant | N-Methyl-o-phenylenediamine | HCID 78498 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | (4-benzyloxy-phenyl)-(1-methyl-1H-benzoimidazol-2-yl)-amine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08318718B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-34bd763df4dc489d8b4c8edd8c7cedab |
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| Source note | uspto-grants-2012_11 |
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