HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 4-Biphenyl-3-yl-N-pyridin-3-ylpiperazine-1-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 1-Biphenyl-3-yl-piperazine | HCID 2756712 | — |
| Reactant | 2,2,2-Trichloroethyl pyridin-3-ylcarbamate | HCID 68575380 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 4-Biphenyl-3-yl-N-pyridin-3-ylpiperazine-1-carboxamide | HCID 16113826 | 58.6% |
Reaction Steps
A mixed solution of 2,2,2-trichloroethyl pyridin-3-ylcarbamate (249 mg, 0.923 mmol), 1-biphenyl-3-ylpiperazine (200 mg, 0.839 mmol) and diisopropylethylamine (0.292 ml, 1.68 mmol) in dimethylsulfoxide (2.5 ml) was stirred at 70° C. for 12 hours. To the reaction solution was added water, and extracted with ethyl acetate. The extract was washed with water, dried over anhydrous magnesium sulfate, and the solvent was distilled away under reduce pressure. The residue was purified by silica gel column chromatography (ethyl acetate), and then recrystallized from a mixed solvent of hexane and ethyl acetate to give the titled compound (176 mg, 58.6%) as solid product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07812025B2 |
| Source dataset | uspto-grants-2010_10 |
| ORD ID | ord-cc1a9d0dbe4844a28381990d54baac16 |
| Source note | uspto-grants-2010_10 |