Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 3-Amino-5-bromopyridine | HCID 817681 | — |
| Reactant | HCID 89886791 | HCID 89886791 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | HCID 57520684 | HCID 57520684 | 45% |
Reaction Steps
Pd(PPh3)4 (0.013 g) was added to a solution of compound (2b) (0.102 g), 3-amino-5-bromopyridine (0.042 g), and an aqueous sodium carbonate solution (2 M, 1.5 mL) in ethylene glycol dimethyl ether (3 mL) in a nitrogen atmosphere, and the mixture was stirred at 85° C. for 3 hours. The reaction solution was partitioned between ethyl acetate and water. The organic layer was washed with brine and then dried over anhydrous sodium sulfate. The solvent was distilled off. An aqueous sodium hydroxide solution (4 M, 0.093 mL) and a 300 aqueous hydrogen peroxide solution (0.045 mL) were added to a solution of the obtained residue in DMSO (3 mL) and ethanol (1.5 mL) at room temperature, and the mixture was stirred for 30 minutes. Water was added to the reaction solution, and the deposit was collected by filtration, then washed with water and ether by sprinkling, and then dried under reduced pressure to obtain compound (2) (0.045 g, yield based on 2 steps: 45%) as a pale yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08912181B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-eebdfcac9ca644caa3fd43584dafdca3 |
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| Source note | uspto-grants-2014_12 |
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