HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoyl chloride → N-[4-(4-Benzoyl-piperazine-1-sulfonyl)-phenyl]-acrylamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | N-[4-(piperazine-1-sulfonyl)-phenyl]-acrylamide | HCID 56953730 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-[4-(4-Benzoyl-piperazine-1-sulfonyl)-phenyl]-acrylamide | HCID 67194760 | 13.3% |
Reaction Steps
Diisopropylethylamine (0.24 ml, 1.36 mmol) was added in one portion to a stirred solution of N-[4-(piperazine-1-sulfonyl)-phenyl]-acrylamide (0.1 g, 0.34 mmol) in THF (5 ml). The mixture was stirred at room temperature for 5 minutes before benzoyl chloride (0.05 ml, 0.44 mmol) was added drop wise and the resulting mixture was stirred at room temperature under a nitrogen atmosphere for 18 hours. The crude reaction mixture was concentrated under vacuum and the residue was purified by Prep HPLC to give the title compound (0.018 g, 13% yield) as a white powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08946197B2 |
| Source dataset | uspto-grants-2015_02 |
| ORD ID | ord-49ca5b650af8410d9a43bb4f4eabda26 |
| Source note | uspto-grants-2015_02 |