HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2263159Generated: October 25, 2026
Water → N-(4-Bromo-1-methyl-1H-pyrazol-5-yl)-4-(3-phenyl-1,2,4-thiadiazol-5-yl)piperazine-1-carboxamide
https://huagongshe.com/reaction/2263159
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 1-(3-Phenyl-(1,2,4)thiadiazol-5-yl)-piperazine | HCID 2777760 | — |
| Reactant | 2,2,2-Trichloroethyl (4-bromo-1-methyl-1H-pyrazol-5-yl)carbamate | HCID 86625505 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | N-(4-Bromo-1-methyl-1H-pyrazol-5-yl)-4-(3-phenyl-1,2,4-thiadiazol-5-yl)piperazine-1-carboxamide | HCID 68780084 | 69.7% |
Reaction Steps
A mixture of 2,2,2-trichloroethyl (4-bromo-1-methyl-1H-pyrazol-5-yl)carbamate (289 mg, 0.822 mmol), 1-(3-phenyl-1,2,4-thiadiazol-5-yl)piperazine (184 mg, 0.747 mmol) and diisopropylethylamine (0.143 ml, 0.822 mmol) in dimethylsulfoxide (2.5 ml) was stirred at 70° C. for 15.5 hours. Water was poured into the reaction solution, and the mixture was extracted with ethyl acetate. The extract was washed with water and dried over anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure. The residue was recrystallized from a mixed solvent of hexane and tetrahydrofuran to give 233 mg (69.7%) of the desired product as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07851473B2 |
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| Source dataset | uspto-grants-2010_12 |
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| ORD ID | ord-2998ecfa1f5341cd8167dfb322885733 |
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| Source note | uspto-grants-2010_12 |
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