HuagongsheHuagongshe Chemistry Print Report · For research reference only
1H-Imidazolium, 2-chloro-4,5-dihydro-1,3-dimethyl-, chloride → (4-tert-butyl-3-fluorophenoxy)-N-((1R)-1-{3-methyl-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 | (4-tert-Butyl-3-fluorophenoxy)acetic acid | HCID 21097504 | — |
| Reactant | N-{4-[(1R)-1-aminoethyl]-2-methylphenyl)methanesulfonamide hydrochloride | HCID 21097519 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | (4-tert-butyl-3-fluorophenoxy)-N-((1R)-1-{3-methyl-4-[(methylsulfonyl)amino]phenyl}ethyl)acetamide | HCID 11590204 | 44% |
Reaction Steps
(4-tert-Butyl-3-fluorophenoxy) acetic acid (153 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-methylphenyl}methanesulfonamide hydrochloride (180 mg, 0.68 mmol) were mixed in the same procedure described in Example 2(b) to give 129 mg (44% yield) of the title compound as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07214824B2 |
| Source dataset | uspto-grants-2007_05 |
| ORD ID | ord-7f72634798ab4ae1b9943a209c7eb766 |
| Source note | uspto-grants-2007_05 |