HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → HCID 52913256, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | N-Iodosuccinimide | HCID 120273 | — |
| Reactant | HCID 52913370 | HCID 52913370 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 52913256 | HCID 52913256 | — |
Reaction Steps
A solution of N-[2-(3-{1-ethyl-5-[4-(trifluoromethyl)phenoxy]-1H-pyrazol-3-yl}phenyl)propan-2-yl]-2,2,2-trifluoroethanesulfonamide (560 mg, 10.5 mmol) and DCM (6.97 mL) was cooled to 0° C., treated with NIS (706 mg, 3.14 mmol) in a single portion. The mixture was protected from light and allowed to warm to rt as it was stirred overnight. The reaction was diluted with EtOAc and washed with water 2×, sat. aq. NaHCO3, brine, dried (MgSO4) and concentrated to afford a white solid purified via MPLC, 25 g silica, 10-60% EtOAc in heptanes to afford a white solid: MS: cal'd 662 (MH+), exp 662 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08871796B2 |
| Source dataset | uspto-grants-2014_10 |
| ORD ID | ord-9fd21b08f5d34fc9b53936e653186a5d |
| Source note | uspto-grants-2014_10 |