HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanesulfonamide → HCID 59520217, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanesulfonamide | HCID 72879 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | P,P-Diphenylphosphinic azide | HCID 199401 | — |
| Reactant | HCID 11717424 | HCID 11717424 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 59520217 | HCID 59520217 | — |
Reaction Steps
A mixture of 3-{cyclopentyl-[4-(4-isopropyl-phenyl)-thiazol-2-yl]-amino}-propionic acid (100 mg, 0.28 mmol), diphenyl phosphoryl azide (70 ul, 0.25 mmol) and DIEA (150 μl) was heated in CH3CN at 60° C. for 1 hour. After cooling to room temperature methane sulfonamide (50 mg, 0.52 mmol) was added and reaction mixture was stirred. After 16 h, the reaction mixture was concentrated in high vacuum. The crude residue was purified on a silica gel column (ethyl acetate/hexane 1:1) to afford 1-(2-{cyclopentyl-[4-(4-isopropyl-phenyl)-thiazol-2-yl]-amino}-ethyl)-3-methanesulfonyl-urea (25 mg). LCMS m/z: 452 (M+1)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07820704B2 |
| Source dataset | uspto-grants-2010_10 |
| ORD ID | ord-d3aa1b6aabf7458f90ffa0856e027e06 |
| Source note | uspto-grants-2010_10 |