HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → HCID 15392250, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 11273480 | HCID 11273480 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 15392250 | HCID 15392250 | 81.1% |
Reaction Steps
Ethyl[N-[4-[(1-t-butoxycarbonyl-4-piperidyl)oxy]phenyl]-N-[(7-cyano-2-naphthyl)methyl]sulfamoyl]acetate (500 mg) was dissolved in 10 ml of acetonitrile, 0.52 ml of methyl iodide and 136 mg of potassium carbonate were added to the solution, and the mixture was stirred under reflux for 5 hours and 30 minutes. After cooling the reaction solution, the precipitate was removed by filtration, and the resulting filtrate was concentrated under a reduced pressure. The resulting residue was applied to silica gel column chromatography, which was eluted with hexane:ethyl acetate (3:1) to give 415 mg of ethyl 2-[N-[4-[(1-t-butoxycarbonyl-4-piperidyl)oxy]phenyl]-N-[(7-cyano-2-naphthyl)methyl]sulfamoyl]propionate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05869501 |
| Source dataset | uspto-grants-1999_02 |
| ORD ID | ord-db29484ce1934f33a90ac24fe27bc3f5 |
| Source note | uspto-grants-1999_02 |