Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nitrogen | HCID 947 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 9-Benzyl-9-borabicyclo(3.3.1)nonane | HCID 4150924 | — |
| Reactant | 3-Chloro-6-(3-fluoro-4-methoxyphenyl)pyridazine | HCID 20398284 | — |
| Catalyst | HCID 178477754 | HCID 178477754 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 57445398 | HCID 57445398 | — |
Reaction Steps
A solution of 3-chloro-6-(3-fluoro-4-methoxy-phenyl)-pyridazine (Step 1, 2.0 g, 8.38 mmol), B-benzyl-9-BBN (0.5 mL in THF, 20 mL) and K2CO3 (3.5 g, 25.1 mmol) in 30 mL of DMF was degassed with N2 for 5 min. Cat. Pd(DPPF)Cl2 (731 mg, 1 mmol) was then added and the reaction was heated at 65° C. for 3 h (preheated oil bath). The mixture was poured into ice water and extracted with 50 mL 2×EtOAc. The combined organic phases were washed with 50 mL of brine and dried over Na2SO4. The solution was concentrated in vacuo and the crude was purified by silica gel column chromatograph (50% EtOAc/Hexane to EtOAc) to give light yellow solid. MS (ESI pos. ion) m/z: 295.3 (M+H). Calc'd Exact Mass for C18H15FN2O: 294.32.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07652009B2 |
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| Source dataset | uspto-grants-2010_01 |
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| ORD ID | ord-b95c7908c6174fc394e4e6df1b1d58b7 |
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| Source note | uspto-grants-2010_01 |
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