HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → HCID 86758624, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | HCID 53732088 | HCID 53732088 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 86758624 | HCID 86758624 | 76.4% |
Reaction Steps
A mixture of (2R)-4-(3-chloropropanesulfonyl)-1-[5-(4-fluorophenyl)thiophene-2-sulfonyl]-N-(2-tetrahydropyranyloxy)-2-piperazinecarboxamide (200 mg), piperidine (279 mg) and potassium iodide (65 mg) in DMF (3 ml) was stirred at ambient temperature for 2 days. The mixture was concentrated in vacuo. The residue was partitioned between AcOEt and H2O. The organic layer was washed with saturated aqueous NaCl solution, dried over MgSO4, and concentrated in vacuo. The residue was purified by SiO2 column chromatography eluted with MeOH in CHCl3 gradually from 0% to 5%, to give 165 mg of (2R)-1-[5-(4-fluorophenyl)thiophene-2-sulfonyl]-4-[3-(-piperidino) propanesulfonyl]-N-(2-tetrahydropyranyloxy)-2-piperazinecarboxamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06489324B2 |
| Source dataset | uspto-grants-2002_12 |
| ORD ID | ord-d1e152bfb2574d3fba3bee412c7eba93 |
| Source note | uspto-grants-2002_12 |