HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → HCID 71251889, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Methylboronic Acid | HCID 139377 | — |
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Reactant | HCID 66524905 | HCID 66524905 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Catalyst | 2-Dicyclohexylphosphino-2',6'-dimethoxybiphenyl | HCID 11269872 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 71251889 | HCID 71251889 | 108.7% |
Reaction Steps
Under a nitrogen stream, to a mixture of 4-(5-bromo-3-cyanopyridin-2-yl)piperazine-1-carboxylic acid tert-butyl ester (1.52 g) described in Preparation Example 105, methylboronic acid (0.50 g), palladium(II) acetate (46 mg), 2-dicyclohexylphosphino-2′,6′-dimethoxybiphenyl (0.17 g) and potassium fluoride (0.96 g) was added tetrahydrofuran (40 mL), and the mixture was stirred with heating under reflux for 8 hr. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, and the solvent was evaporated. The obtained residue was purified by silica gel column chromatography (hexane:ethyl acetate) to give the title compound (1.36 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08816079B2 |
| Source dataset | uspto-grants-2014_08 |
| ORD ID | ord-5db5ff3d587c408d8997ed0186d503fa |
| Source note | uspto-grants-2014_08 |