Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | Dimethylacetamide | HCID 31374 | — |
| Reactant | Methyl 3,4-difluorobenzoate | HCID 2775358 | — |
| Reactant | HCID 67983256 | HCID 67983256 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 67983240 | HCID 67983240 | — |
Reaction Steps
The amine, 4-((8-azabicyclo[3.2.1]octan-3-yloxy)methyl)-5-cyclopropyl-3-(2-(trifluoromethoxy)phenyl)isoxazole (41.5 mg, 0.102 mmol), dimethylacetamide (0.6 mL), methyl 3,4 difluorobenzoate (510 mg, 3.0 mmol), and cesium carbonate (108 mg, 0.33 mmol) were combined sequentially and heated to 100° C. for about 20 minutes and then 120° C. for approximately 1 hour. The mixture was diluted with ethyl acetate 20 mL and water washed (2×3 mL). The organics were dried under vacuum to a residue, the resulting residue was diluted with 3 mL of MeOH, and the liquid was directly purified using mass directed reverse phase HPLC under a gradient of 30 to 90% acetonitrile/water that was TFA modified (0.05%). The resulting product was cold vacuum concentrated and free based using an SPE polymer support cartridge and MeOH (5 mL) mobilizing solvent (product SPE PLHCO3 MP part no PL3540-C603). All resulting methanol effluent was concentrated to give the free based intermediate ester as a dense oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09150568B2 |
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| Source dataset | uspto-grants-2015_10 |
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| ORD ID | ord-dc46c77778954972b41497e1d9329d25 |
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| Source note | uspto-grants-2015_10 |
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