HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 4-[4-(4-Fluorophenyl)-1,3-thiazol-2-yl]-N-pyrazin-2-ylpiperazine-1-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 1-[4-(4-Fluorophenyl)-2-thiazolyl]piperazine | HCID 8027201 | — |
| Reactant | 2,2,2-Trichloroethyl pyrazin-2-ylcarbamate | HCID 68777403 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 4-[4-(4-Fluorophenyl)-1,3-thiazol-2-yl]-N-pyrazin-2-ylpiperazine-1-carboxamide | HCID 68779098 | 34.1% |
Reaction Steps
A mixture if 2,2,2-trichloroethyl pyrazin-2-ylcarbamate (226 mg, 0.835 mmol), 4-[4-(4-fluorophenyl)-1,3-thiazol-2-yl]piperazine (200 mg, 0.760 mmol) and diisopropylethylamine (0.265 ml, 1.52 mmol) in dimethylsulfoxide (2.5 ml) was stirred at 70° C. for 3 days. Water was poured into the reaction solution, and the mixture was extracted with ethyl acetate. The extract was wash washed with water and dried over anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure. The residue was purified silica gel column chromatography (ethyl acetate) and recrystallized from a mixed solvent of hexane and tetrahydrofuran to give the desired product (99.7 mg, 34.0%) as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07851473B2 |
| Source dataset | uspto-grants-2010_12 |
| ORD ID | ord-996151c7ada64869bae11e6fd38fd5fa |
| Source note | uspto-grants-2010_12 |