HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethyl Sulfoxide → 4-(3-Phenyl-1,2,4-thiadiazol-5-yl)-N-[4-(1H-pyrazol-1-yl)phenyl]piperazine-1-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 1-[3-(2-Fluorophenyl)-1,2,4-thiadiazol-5-yl]piperazine | HCID 68775720 | — |
| Reactant | 2,2,2-Trichloroethyl [4-(1H-pyrazol-1-yl)phenyl]carbamate | HCID 86245202 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-(3-Phenyl-1,2,4-thiadiazol-5-yl)-N-[4-(1H-pyrazol-1-yl)phenyl]piperazine-1-carboxamide | HCID 68776373 | — |
Reaction Steps
A solution of 2,2,2-trichloroethyl [4-(1H-pyrazol-1-yl)phenyl]carbamate (200 mg, 0.598 mmol), 1-[3-(2-fluorophenyl)-1,2,4-thiadiazol-5-yl]piperazine (147 mg, 0.598 mmol), diisopropylethylamine (0.208 ml, 1.20 mmol) and dimethyl sulfoxide (4 ml) was stirred at 70° C. for 24 hours, the reaction mixture was poured into water, and the mixture was extracted with ethyl acetate. The extract was washed with water, and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure, and the residue was purified by silica gel column chromatography (ethyl acetate) to give the desired product as a solid. The solid was recrystallized from ethyl acetate to give 63.7 mg (24.7%) of the desired product as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07851473B2 |
| Source dataset | uspto-grants-2010_12 |
| ORD ID | ord-ebd64d3764084d729889c50b509fed72 |
| Source note | uspto-grants-2010_12 |