HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-{4-[3-(4-t-butyl-benzyl)-ureidomethyl]-2-fluoro-6-vinyl-phenyl}methanesulfonamide → N-{4-[3-(4-t-butylbenzyl)ureidomethyl]-2-ethyl-6-fluorophenyl}methanesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-{4-[3-(4-t-butyl-benzyl)-ureidomethyl]-2-fluoro-6-vinyl-phenyl}methanesulfonamide | HCID 11852379 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N-{4-[3-(4-t-butylbenzyl)ureidomethyl]-2-ethyl-6-fluorophenyl}methanesulfonamide | HCID 11851687 | 100% |
Reaction Steps
N-{4-[3-(4-t-butyl-benzyl)-ureidomethyl]-2-fluoro-6-vinyl-phenyl}methanesulfonamide (15.6 mg, 0.04 mmol) was dissolved in methanol. To the solution was added Pd/C (10 wt. %) and air in the flask was displaced with hydrogen gas. The reaction solution was stirred for 1 hour. After confirming the completion of the reaction with TLC, Pd/C was filtered off through celite. The methanol was removed under reduced pressure and column-chromatographed (n-hexane/ethyl acetate ˜1/1) to yield a white solid (15.8 mg, 100.0%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07960584B2 |
| Source dataset | uspto-grants-2011_06 |
| ORD ID | ord-6494be783fa84cf58ec68f3733ba02f7 |
| Source note | uspto-grants-2011_06 |