Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | (Pyridin-4-yl)boronic acid | HCID 2734379 | — |
| Reactant | HCID 68183139 | HCID 68183139 | — |
| Catalyst | Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+) | HCID 178418228 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 68183266 | HCID 68183266 | 13.7% |
Reaction Steps
To a 20 mL vial was added a solution of 2-bromo-4-(4-chlorophenyl)-5,5-dimethyl-5,6-dihydrothieno[2,3-c]pyridin-7(4H)-one (0.0440 g, 0.119 mmol) and pyridine-4-boronic acid (0.02726 g, 0.2218 mmol) in 1,4-dioxane (3.0 mL) and water (0.300 mL). Cesium carbonate (0.1160 g, 0.3561 mmol) was added followed by [1,1′-bis(diphenylphosphino)ferrocene]palladium(II)dichloride (0.0117 g, 0.0142 mmol). The reaction mixture was heated to 90° C. and allowed to stir for 18 h. The reaction was cooled to ambient temperature and quenched by the addition of a saturated aqueous solution of sodium bicarbonate (10 mL) and extracted with EtOAc (10 mL×3). The combined organic layers were dried over anhydrous Na2SO4, filtered and concentrated under reduced pressure. The crude material as purified by prep HPLC to afford the product (0.0060 g, 13%) as a yellow solid. LC/MS (AA) ES+ 369, 371, 373. 1H NMR (dmso-d6, 400 MHz): d 8.59-8.57 (2H, m), 7.91 (1H, s), 7.68-7.66 (2H, m), 7.60 (1H, s), 7.40-7.38 (2H, m), 7.19-7.17 (2H, m), 4.21 (1H, s), 1.36 (3H, s), 0.94 (3H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08765746B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-eb80030f79ae4043afc884143033a3c9 |
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| Source note | uspto-grants-2014_07 |
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