HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 2-(4((6-Chloro-2-quinoxalinyl)oxy)phenoxy)-N-(4-(1,1-difluoro-2,2,2-trichloroethoxy)phenyl)propanamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 13370018 | HCID 13370018 | — |
| Reactant | 4-(1,1-Difluoro-2,2,2-trichloroethoxy)aniline | HCID 13529255 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2-(4((6-Chloro-2-quinoxalinyl)oxy)phenoxy)-N-(4-(1,1-difluoro-2,2,2-trichloroethoxy)phenyl)propanamide | HCID 19792683 | — |
Reaction Steps
A solution of 4.35 mmol of 2-(4-((6-chloro-2-quinoxalinyl)oxy)phenoxy)propanoyl chloride (previously prepared from 1.5 g of the corresponding acid) in 15 ml of acetonitrile was added to a mixture prepared from 1.20 g (4.35 mmol) of 4-(1,1-difluoro-2,2,2-trichloroethoxy)aniline, 0.66 g (6.5 mmol) of triethylamine and 10 ml of acetonitrile. The mixture was warmed at reflux for a period of 2.5 hours and then poured over ice and aqueous NaOH added. The resulting precipitate was filtered and dried and then recrystallized from methylcyclohexane. This left 2.2 g (84 percent of theoretical) of the above-named product as a brown solid, m.p. 139°-141° C. (Compound 36)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05250690 |
| Source dataset | uspto-grants-1993_10 |
| ORD ID | ord-cad06a10c03645768c61673b4daa1778 |
| Source note | uspto-grants-1993_10 |