HuagongsheHuagongshe Chemistry Print Report · For research reference only
1H-Imidazolium, 2-chloro-4,5-dihydro-1,3-dimethyl-, chloride → 3-Chloro-4-(trifluoromethyl)phenoxyl-N-{3-methyl-4-[(methylsulfonyl)amino]benzyl}acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1H-Imidazolium, 2-chloro-4,5-dihydro-1,3-dimethyl-, chloride | HCID 10986715 | — |
| Reactant | [3-Chloro-4-(trifluoromethyl)phenoxy]acetic acid | HCID 21097484 | — |
| Reactant | N-[4-(aminomethyl)-2-methylphenyl]methanesulfonamide hydrochloride | HCID 21097529 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 3-Chloro-4-(trifluoromethyl)phenoxyl-N-{3-methyl-4-[(methylsulfonyl)amino]benzyl}acetamide | HCID 11669592 | 67% |
Reaction Steps
[3-Chloro-4-(trifluoromethyl)phenoxy]acetic acid (127 mg, 0.5 mmol), 2-chloro-1,3-dimethylimidazolinium chloride (CDI) (97 mg, 0.6 mmol), triethylamine (0.33 ml) and N{4-(aminomethyl)-2-methylphenyl]methanesulfonamide hydrochloride (151 mg, 0.6 mmol) were treated in the same procedure described in Example 2(b). The crude residue was applied to a silica gel chromatography column and eluted with a volume mixture of hexane and ethyl acetate (3/1 to 1/1) to furnish 150 mg (67% 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-37b36ae4724240e8a28d897160a28d48 |
| Source note | uspto-grants-2007_05 |