HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethyl Sulfoxide → N-Isoxazol-5-yl-4-(4-phenyl-1,3-thiazol-2-yl)piperazine-1-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 1-(4-Phenyl-1,3-thiazol-2-yl)piperazine | HCID 712468 | — |
| Reactant | 2,2,2-Trichloroethyl isoxazol-5-ylcarbamate | HCID 68776411 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-Isoxazol-5-yl-4-(4-phenyl-1,3-thiazol-2-yl)piperazine-1-carboxamide | HCID 68778074 | — |
Reaction Steps
A solution of 2,2,2-trichloroethyl isoxazol-5-ylcarbamate (200 mg, 0.771 mmol), 1-(4-phenyl-1,3-thiazol-2-yl)piperazine (189 mg, 0.771 mmol), diisopropylethylamine (0.134 ml, 0.771 mmol) and dimethylsulfoxide (7 ml) was stirred at 70° C. for 12 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. The residue was purified by silica gel column chromatography (ethyl acetate) to obtain the desired product as a solid. This was recrystallized from a mixed solvent of ethyl acetate and hexane to obtain the desired product (98.8 mg, 36.1%) as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07851473B2 |
| Source dataset | uspto-grants-2010_12 |
| ORD ID | ord-c974ec2f109c4d4a86a6aef67263cee2 |
| Source note | uspto-grants-2010_12 |