HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Iodide → 1-(2,6-Difluoro-benzyl)-3-[4-(4-formyl-piperidine-1-sulfonyl)-phenyl]-1-isopropyl-urea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | 1-(2,6-Difluoro-benzyl)-3-[4-(4-dimethoxymethyl-piperidine-1-sulfonyl)-phenyl]-1-isopropyl-urea | HCID 18678484 | — |
| Reactant | CID 71317501 | HCID 71317501 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 1-(2,6-Difluoro-benzyl)-3-[4-(4-formyl-piperidine-1-sulfonyl)-phenyl]-1-isopropyl-urea | HCID 18678525 | — |
Reaction Steps
Under anhydrous conditions, a solution of 1-(2,6-difluoro-benzyl)-3-[4-(4-dimethoxymethyl-piperidine-1-sulfonyl)-phenyl]-1-isopropyl-urea (0.32 g, 0.6 mmol), sodium iodide (0.228 g, 1.5 mmol), and trichloromethylsilane (0.143 mL, 1.2 mmol) in acetonitrile (2.5 mL) was stirred at ambient temperature for 15 minutes. The reaction mixture was quenched with water and partitioned with methylene chloride. The organic phase was washed with Na2S2O3 dilute solution and dried (Na2SO4). Removal of solvent afforded the crude product which was used directly in the next step without characterization.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06506901B2 |
| Source dataset | uspto-grants-2003_01 |
| ORD ID | ord-9c102a2e3fef44f5b81767859290d234 |
| Source note | uspto-grants-2003_01 |