Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | Pyridine-2-boronic acid, pinacol ester | HCID 11241171 | — |
| Reactant | HCID 90409003 | HCID 90409003 | — |
| Catalyst | Cupric Chloride | HCID 24014 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Catalyst | Ferrocene-1,1'-bis-(diphenylphosphine) | HCID 635956 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 90408677 | HCID 90408677 | 17.7% |
Reaction Steps
To a solution of tert-butyl 2-methyl-3-(((trifluoromethyl)sulfonyl)oxy)-4,5-dihydro-2H-pyrazolo[3,4-c]pyridine-6(7H)-carboxylate (1.0 g, 2.60 mmol) in DMF (25 mL) was added pyridine-2-boronic acid pinacol ester (1.33 g, 6.49 mmol), cesium carbonate (3.42 g, 10.38 mmol), copper chloride (257 mg, 0.259 mmol), palladium acetate (29 mg, 0.130 mmol) and 1,1′-bis(diphenylphosphino)ferrocene (145 mg, 0.259 mmol). The reaction was stirred at 100° C. overnight under an atmosphere of N2. The reaction was poured into ice water and extracted with CH2Cl2 three times. The combined organic layers were dried over anhydrous MgSO4, filtered and evaporated. Chromatography on silica gel (0-100% ethyl acetatehexanes) provided the desired product (145 mg, 17%). MS (ESI) mass calcd. C17H22N4O2, 314.2. m/z found, 315.2 [M+H]+. 1H NMR (500 MHz, CDCl3) δ 8.73-8.70 (m, 0.5H), 7.80-7.76 (m, 0.5H), 7.40-7.35 (m, 2H), 7.31-7.24 (m, 1H), 4.66-4.44 (m, 2H), 4.07 (s, 2H), 3.84 (s, 1H), 3.70-3.56 (m, 2H), 2.73-2.55 (m, 2H), 1.54-1.42 (m, 9H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09066946B2 |
|---|
| Source dataset | uspto-grants-2015_06 |
|---|
| ORD ID | ord-13eb0e0d33be4cc99f633157ff97edd0 |
|---|
| Source note | uspto-grants-2015_06 |
|---|