HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 586157Generated: October 25, 2026
Triethylamine → N-[4-({[2-(4-Bromophenyl)-5,7-dimethylimidazo[5,1-f][1,2,4]triazin-4-yl]amino}-methyl)phenyl]acetamide
https://huagongshe.com/reaction/586157
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | N-[4-(aminomethyl)phenyl]acetamide | HCID 15295869 | — |
| Reactant | 2-(4-Bromophenyl)-5,7-dimethyl-4-(1H-1,2,4-triazol-1-yl)imidazo[5,1-f][1,2,4]triazine | HCID 22329622 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | N-[4-({[2-(4-Bromophenyl)-5,7-dimethylimidazo[5,1-f][1,2,4]triazin-4-yl]amino}-methyl)phenyl]acetamide | HCID 22329639 | — |
Reaction Steps
2-(4-Bromophenyl)-5,7-dimethyl-4-(1H-1,2,4-triazol-1-yl)imidazo[5,1-f][1,2,4]-triazine (3.7 mg, 10 mmol) is treated in dioxane (100 μl) with 4-acetylamino-benzylamine (3.3 mg, 20 mmol) and triethylamine (4 μl). The mixture is heated at 80° C. with shaking for 12 h, filtered and washed with DMSO (2×100 μl). The combined filtrates are purified chromatographically by preparative LC-MS.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06936609B2 |
|---|
| Source dataset | uspto-grants-2005_08 |
|---|
| ORD ID | ord-220a3115004a4a9fa2dfcefbfc7be50a |
|---|
| Source note | uspto-grants-2005_08 |
|---|