HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thiophene-2-sulfonyl isocyanate → N-[N-[4-(2,2,2-trifluoroethoxy)-6-methylpyrimidin-2-yl]-N-methylaminocarbonyl]-2-thiophenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thiophene-2-sulfonyl isocyanate | HCID 12875192 | — |
| Reactant | 2-Methylamino-4-(2,2,2-trifluorethoxy)-6-methylpyrimidine | HCID 20189867 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-[N-[4-(2,2,2-trifluoroethoxy)-6-methylpyrimidin-2-yl]-N-methylaminocarbonyl]-2-thiophenesulfonamide | HCID 20189874 | — |
Reaction Steps
To a dry stirred solution of 22.1 parts of 2-methylamino-4-(2,2,2-trifluorethoxy)-6-methylpyrimidine in 250 parts of methylene chloride at ambient temperature was added 18.9 parts of 2-thiophenesulfonyl isocyanate. That mixture was stirred and refluxed for 2 hours. The methylene chloride was removed under reduced pressure, and the resulting solid was triturated with toluene to yield 19 parts of N-[N-[4-(2,2,2-trifluoroethoxy)-6-methylpyrimidin-2-yl]-N-methylaminocarbonyl]-2-thiophenesulfonamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04501607 |
| Source dataset | uspto-grants-1985_02 |
| ORD ID | ord-2249d046f29e4837947070fa9c45cdd0 |
| Source note | uspto-grants-1985_02 |