HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Tert-butyl-4-isocyanatobenzene → N-{4-[3-(4-tert-Butylphenyl)ureidomethyl]-2-fluoro-6-vinylphenyl}methanesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Tert-butyl-4-isocyanatobenzene | HCID 2735695 | — |
| Reactant | HCID 57665528 | HCID 57665528 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-{4-[3-(4-tert-Butylphenyl)ureidomethyl]-2-fluoro-6-vinylphenyl}methanesulfonamide | HCID 11853001 | 56.6% |
Reaction Steps
N-(4-Aminomethyl-2-fluoro-6-vinylphenyl)methanesulfonamide (37.8 mg, 0.11 mmol), 1-tert-butyl-4-isocyanatobenzene (1.2 eq, 0.13 mmol, 22.49 μl), and TEA (3 eq, 0.33 mmol, 45.99 μl) were added in methylene chloride. The reaction mixture was stirred for 12 hrs. The reaction mixture was extracted with methylene chloride. A combined organic layer was washed with H2O and brine, dried over Na2SO4, and concentrated in vacuo. The residue was purified with column chromatography (n-Hx:EA=1:1) to yield title compound (26.1 mg, 55%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07763657B2 |
| Source dataset | uspto-grants-2010_07 |
| ORD ID | ord-508ca1d30fe643ab963c69de6623e90a |
| Source note | uspto-grants-2010_07 |