Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | (Pyridin-4-yl)boronic acid | HCID 2734379 | — |
| Reactant | HCID 67107764 | HCID 67107764 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | HCID 68108451 | HCID 68108451 | — |
Reaction Steps
To a microwave vial was added 5-bromo-2-([(3,4-difluorophenyl)methyl]oxy)-N-4-pyridazinylbenzamide (may be prepared as described in Example 78; 200 mg, 0.48 mmol), 4-pyridinylboronic acid (88 mg, 0.74 mmol), tetrakis(triphenylphosphine)palladium(0) (33.0 mg, 0.03 mmol), sodium carbonate (0.95 ml, 0.95 mmol) and 1,2-dimethoxyethane (3 ml). The mixture was sealed and heated to 120° C. for 1 hour under microwave conditions. The 1,2-dimethoxyethane was evaporated under reduced pressure and the residue was purified using MDAP to yield the title compound. 35 mg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08778939B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-278ca2ed6e354afdacbcb78b27389a02 |
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| Source note | uspto-grants-2014_07 |
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