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-{3-fluoro-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]-2-fluorophenyl}methanesulfonamide hydrochloride | HCID 66841089 | — |
| 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-{3-fluoro-4-[(methylsulfonyl)amino]phenyl}ethyl)acetamide | HCID 57762923 | 37% |
Reaction Steps
(4-tert-Butyl-3,5-difluorophenoxy)acetic acid (166 mg, 0.68 mmol), 2-chloro-1,3-dimethylimidazolinium chloride (CDI) (110 mg, 0.68 mmol), triethylamine (0.5 ml) and N-{4-[(1R)-1-aminoethyl]-2-fluorophenyl}methanesulfonamide hydrochloride (183 mg, 0.68 mmol) were mixed by the same procedure as described in Example 1(e) to give 115 mg (37%) 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-958f5bc5e2c7406e8a469acd75604569 |
| Source note | uspto-grants-2009_07 |