Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenol | HCID 996 | — |
| Reactant | Butyronitrile | HCID 8008 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | HCID 58118934 | HCID 58118934 | — |
| Reactant | HCID 58118986 | HCID 58118986 | — |
| Product | HCID 58119008 | HCID 58119008 | — |
Reaction Steps
In a sealable flask, a suspension of the phenol, 4-(3-(trifluoromethyl)-[1,2,4]triazolo[4,3-a]pyridin-6-yl)phenol, prepared as described in Example 1 (47 mg, 0.17 mmol), heteroaryl chloride (39 mg, 0.34 mmol), Cs2CO3 (111 mg, 0.34 mmol), and butyronitrile (1 mL) is heated to 140° C. overnight. The reaction is concentrated and purified by RP-HPLC to afford the desired product, 6-(4-(pyridazin-3-yloxy)phenyl)-3-(trifluoromethyl)-[1,2,4]triazolo[4,3-a]pyridine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08754103B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-16749065b32e4c269868dcff6895e94b |
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| Source note | uspto-grants-2014_06 |
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