HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 4-[3-(3-Furyl)-1,2,4-thiadiazol-5-yl]-N-pyridin-4-ylpiperazine-1-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2,2,2-Trichloroethyl pyridin-4-ylcarbamate | HCID 14257294 | — |
| Reactant | 1-[3-(3-Furyl)-1,2,4-thiadiazol-5-yl]piperazine | HCID 68777843 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 4-[3-(3-Furyl)-1,2,4-thiadiazol-5-yl]-N-pyridin-4-ylpiperazine-1-carboxamide | HCID 68782017 | 30.8% |
Reaction Steps
A mixed solution of 2,2,2-trichloroethyl pyridin-4-ylcarbamate (207 mg, 0.770 mmol), 1-[3-(3-furyl)-1,2,4-thiadiazol-5-yl]piperazine (200 mg, 0.846 mmol) and diisopropylethylamine (0.134 ml, 0.846 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) and recrystallized from a mixed solvent of hexane and tetrahydrofuran to give 84.5 mg (30.8%) 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-debbd1bacb3747469b526ff26c86f440 |
| Source note | uspto-grants-2010_12 |