HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2262983Generated: November 1, 2026
Water → N-pyridin-3-yl-4-(3-pyridin-2-yl-1,2,4-thiadiazol-5-yl)piperazine-1-carboxamide
https://huagongshe.com/reaction/2262983
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2,2,2-Trichloroethyl pyridin-3-ylcarbamate | HCID 68575380 | — |
| Reactant | 1-(3-Pyridin-2-yl-1,2,4-thiadiazol-5-yl)piperazine | HCID 68778093 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | N-pyridin-3-yl-4-(3-pyridin-2-yl-1,2,4-thiadiazol-5-yl)piperazine-1-carboxamide | HCID 68777295 | 38.6% |
Reaction Steps
A mixed solution of 2,2,2-trichloroethyl pyridin-3-ylcarbamate (297 mg, 1.10 mmol), 1-(3-pyridin-2-yl-1,2,4-thiadiazol-5-yl)piperazine (300 mg, 1.21 mmol) and diisopropylethylamine (0.211 ml, 1.21 mmol) in dimethyl sulfoxide (2.5 ml) was stirred at 80° C. for 3 hours. Water was poured to the reaction mixture, and the resulting solution 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 purified by silica gel column chromatography (ethyl acetate:hexane=1:1, followed by ethyl acetate:methanol=9:1) and recrystallized from a mixed solvent of hexane and tetrahydrofuran to give 156 mg (38.5%) 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-d159a85e85cb45a9a50832a5bc27bf46 |
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| Source note | uspto-grants-2010_12 |
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