HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → HCID 86684858, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Pyridinylboronic acid | HCID 2734378 | — |
| Reactant | HCID 86684859 | HCID 86684859 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 86684858 | HCID 86684858 | 143.2% |
Reaction Steps
A mixture of 4-(1-methyl-1H-pyrazol-5-yl)phenyl trifluoromethanesulfonate (200 mg), 3-pyridylboronic acid (88 mg), bis(triphenylphosphine)palladium(II) dichloride (14 mg), potassium carbonate (135 mg), dimethylformamide (1.4 mL) and ethanol (0.70 mL) was reacted in a microwave reactor (80° C., 25 minutes). Thereafter, water was added to the reaction solution, and the obtained mixture was extracted with ethyl acetate. The organic layer was washed with water and a saturated saline, and was then dried over anhydrous magnesium sulfate, followed by vacuum concentration, so as to obtain the title compound (220 mg) in the form of a light yellow oily substance.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08642626B2 |
| Source dataset | uspto-grants-2014_02 |
| ORD ID | ord-0f255a4b4d6540c38f196799fffa10f6 |
| Source note | uspto-grants-2014_02 |