HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → N-(1,1-Dioxido-1-benzothien-6-yl)-4-[3-(2-thienyl)-1,2,4-thiadiazol-5-yl]piperazine-1-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 1-[3-(Thiophen-2-yl)-1,2,4-thiadiazol-5-yl]piperazine | HCID 68778015 | — |
| Reactant | 2,2,2-Trichloroethyl (1,1-dioxido-1-benzothien-6-yl)carbamate | HCID 86625487 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | N-(1,1-Dioxido-1-benzothien-6-yl)-4-[3-(2-thienyl)-1,2,4-thiadiazol-5-yl]piperazine-1-carboxamide | HCID 68777960 | — |
Reaction Steps
A mixed solution of 2,2,2-trichloroethyl (1,1-dioxido-1-benzothien-6-yl)carbamate (257 mg, 0.720 mmol), 1-[3-(2-thienyl)-1,2,4-thiadiazol-5-yl]piperazine (200 mg, 0.792 mmol) and diisopropylethylamine (0.129 ml, 0.720 mmol) in dimethyl sulfoxide (2.5 ml) was stirred at 70° 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. Chloroform was added to the residue, and 69.6 mg (21.0%) of the desired product as a solid was separated by filtration.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07851473B2 |
| Source dataset | uspto-grants-2010_12 |
| ORD ID | ord-5cf900c58ab241ab9faaf550b72ec063 |
| Source note | uspto-grants-2010_12 |