HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 1-((6-methoxypyridin-2-yl)methyl)-4-nitro-3-vinyl-1H-indazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Potassium vinyltrifluoroborate | HCID 23679353 | — |
| Reactant | 3-iodo-1-((6-methoxypyridin-2-yl)methyl)-4-nitro-1H-indazole | HCID 67261104 | — |
| Solvent | Tetrahydrofuran 2-propanol | HCID 22597222 | — |
| Product | 1-((6-methoxypyridin-2-yl)methyl)-4-nitro-3-vinyl-1H-indazole | HCID 67260047 | 94.3% |
Reaction Steps
To 3-iodo-1-((6-methoxypyridin-2-yl)methyl)-4-nitro-1H-indazole (2.65 g, 6.46 mmol) in IPA/THF (40 mL/10 mL) was added potassium vinyltrifluoroborate (1.30 g, 9.69 mmol), triethylamine (1.31 g, 12.9 mmol) and 1,1′-Bis(diphenylphosphino)ferrocene-palladium(II)dichloride dichloromethane complex (0.264 g, 0.323 mmol). The reaction mixture was heated to reflux and stirred for 16 hours. The reaction mixture was cooled to ambient temperature and concentrated to remove solvent. The residue was dissolved with EtOAc (100 mL) and washed with saturated NH4Cl, H2O and brine. The solution was dried (Na2SO4) and concentrated to provide the desired product (1.89 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08841455B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-50f8bd1d9677421285b40aec032841ed |
| Source note | uspto-grants-2014_09 |