Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isopropanol | HCID 3776 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Cesium fluoride | HCID 25953 | — |
| Reactant | 1,3-DIMETHYL-5-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)-1H-PYRAZOLE | HCID 4912748 | — |
| Reactant | HCID 86707518 | HCID 86707518 | — |
| Catalyst | CID 53485975 | HCID 53485975 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 86707517 | HCID 86707517 | 74% |
Reaction Steps
A mixture of tert-butyl (S)-1-((R)-1-(3-(7-bromo-6-fluoro quinolin-2-yl)-[1,2,4]triazolo[4,3-a]pyridin-6-yl)-2,2,2-trifluoroethyl)pyrrolidin-3-ylcarbamate (0.10 g, 0.16 mmol), 1,3-dimethyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole (0.073 g, 0.33 mmol) and cesium fluoride (0.065 g, 0.43 mmol) in 2-propanol (3.3 mL, 0.16 mmol) was degassed with nitrogen. Maintaining a nitrogen atmosphere, triethylamine (0.034 mL, 0.25 mmol) and dichloro[1,1′-bis(diphenylphosphino)ferrocene]palladium(II) dichloromethane adduct (0.013 g, 0.016 mmol) were added, and the vessel sealed and heated at 100° C. for 17 hours. After cooling, the reaction mixture was diluted with ethyl acetate (10 mL), filtered through a plug of Celite®, and concentrated under reduced pressure. Purification of the residue by reverse phase chromatography on a C18 column (0-100% acetonitrile/water) provided the title compound (0.074 g, 72%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08889704B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-9d98199c0730446eaee034056759c44a |
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| Source note | uspto-grants-2014_11 |
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