Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | HCID 69039478 | HCID 69039478 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 69037266 | HCID 69037266 | 94.6% |
Reaction Steps
Methanesulfonyl chloride (0.17 ml) was added to an ice-cooled mixture of 1-benzyl-1-(2-hydroxyethyl)-3-(4-trifluoromethyl-3-pyridylcarbonyl)urea (0.70 g), and triethylamine (0.64 ml) in dichloromethane, then stirred for 3 hours at 20° C. The mixture was washed (water), dried (magnesium sulfate), evaporated and the residue purified by silica-gel chromatography, eluting with n-hexane/ethyl acetate (3:2), to give 1-benzyl-3-(4-trifluoromethyl-3-pyridylcarbonyl)-2-imidazolidinone (0.63 g, Compound S-15).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07476685B2 |
|---|
| Source dataset | uspto-grants-2009_01 |
|---|
| ORD ID | ord-062906c0f4ff40a78f92d7bf4273c541 |
|---|
| Source note | uspto-grants-2009_01 |
|---|