HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanesulfonyl chloride → HCID 11141002, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | MLS002695130 | HCID 260790 | — |
| Reactant | Triethylammonium | HCID 1385867 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 11141002 | HCID 11141002 | 36.2% |
Reaction Steps
A solution of methanesulfonyl chloride (1.4 ml) in DMF (20 ml) was dropped into a stirred suspension of the triethylammonium salt of 5-benzyl-2,4,6-(1H,3H)-pyrimidinetrione (g 5) in DMF (210 ml). After an hour most of the solvent was removed in vacuo. The residual suspension was then poured into a ice-water mixture, and the precipitated white solid was collected by filtration, to yield, after drying, the title product, (4 g, 36.2% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05286861 |
| Source dataset | uspto-grants-1994_02 |
| ORD ID | ord-44ced6f367444c06980200f615f3d830 |
| Source note | uspto-grants-1994_02 |