Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-(Trifluoromethyl)anilinium chloride | HCID 2723961 | — |
| Reactant | 2-(4-((6-Chloro-2-quinoxalinyl)oxy)phenoxy)propanoyl chloride | HCID 13370018 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 15070166 | HCID 15070166 | — |
Reaction Steps
A solution of 7.25 mmol of 2-(4-((6-chloro-2-quinoxalinyl)oxy)phenoxy)propionyl chloride, prepared using substantially the procedure of Step A of Example 1 from the corresponding acid, in 20 ml of acetonitrile was added to solution of 1.43 g (7.25 mmol) of 4-aminobenzotrifluoride, hydrochloride and 1.83 g (18.1 mmol) of triethylamine in 10 ml of acetonitrile. The reaction mixture was warmed at reflux for a period of 4 hours and then poured over crushed ice. The resulting precipitate was collected by filtration and then recrystallized from acetonitrile to give 2.40 g (68 percent of theoretical) of the above-named product as a tan solid which melted at 176°-178° C. The structure of the product was confirmed by its IR and NMR spectrum. (Compound 5)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04968343 |
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| Source dataset | uspto-grants-1990_11 |
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| ORD ID | ord-2c9e7a373d2d492894c8e89dd98de2f0 |
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| Source note | uspto-grants-1990_11 |
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