HuagongsheHuagongshe Chemistry Print Report · For research reference only
1H-Imidazolium, 2-chloro-4,5-dihydro-1,3-dimethyl-, chloride → 2-(4-tert-butyl-3,5-difluorophenoxy)-N-((1R)-1-{4-[(methylsulfonyl)amino]phenyl}ethyl)acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1H-Imidazolium, 2-chloro-4,5-dihydro-1,3-dimethyl-, chloride | HCID 10986715 | — |
| Reactant | N-{4-[(1R)-1-aminoethyl]phenyl}methanesulfonamide hydrochloride | HCID 66978143 | — |
| Reactant | (4-tert-Butyl-3,5-difluorophenoxy)acetic acid | HCID 68804332 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 2-(4-tert-butyl-3,5-difluorophenoxy)-N-((1R)-1-{4-[(methylsulfonyl)amino]phenyl}ethyl)acetamide | HCID 57762916 | 63.2% |
Reaction Steps
((4-tert-Butyl-3,5-difluorophenoxy)acetic acid (147 mg, 0.60 mmol), 2-chloro-1,3-dimethylimidazolinium chloride (CDI) (102 mg, 0.63 mmol), triethylamine (0.5 ml) and N-{4-[(1R)-1-aminoethyl]phenyl}methanesulfonamide hydrochloride (150 mg, 0.60 mmol) were mixed by the same procedure as described in Example 1(e) to give 167 mg (63%) of the title compound as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07566739B2 |
| Source dataset | uspto-grants-2009_07 |
| ORD ID | ord-e9963e10408141e08e969ae1b608a81f |
| Source note | uspto-grants-2009_07 |