Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1,3-Bis(diphenylphosphino)propane | HCID 81219 | — |
| Reactant | HCID 86608615 | HCID 86608615 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 67520578 | HCID 67520578 | — |
Reaction Steps
To a solution of 7-(6,7-dimethoxyquinolin-4-yloxy)naphthalen-2-yl trifluoromethanesulfonate (Step b, 1.0 g, 2.08 mmol) in DMF (10 mL) in a sealed tube, Pd(OAc)2 (0.094, 0.416 mmol) was added, followed by DPPP (0.257 g, 0.624 mmol). CO(g) was bubbled through the mixture for 5 min, and MeOH (2 mL) and Et3N (0.58 mL, 4.16 mmol) was added. The tube was sealed and the mixture was stirred at 70° C. for 2 h. The reaction was diluted with water and extracted with EtOAc 3×. The combined organic layer was washed with water and brine, dried over MgSO4, filtered and concentrated in vacuo. The crude material was taken on directly without purification. MS (ESI, pos. ion) m/z: 390.2 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08178557B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-a314000cdb5449b3adb1cc8122fc29bd |
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| Source note | uspto-grants-2012_05 |
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