Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Bromopyridine | HCID 7973 | — |
| Reactant | HCID 22181052 | HCID 22181052 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 22181068 | HCID 22181068 | 20% |
Reaction Steps
To a suspension of 3-chloro-4-(piperidin-4-yloxy)nitrobenzene (3.00 g) obtained in reference example 8 in pyridine (30 ml) was added 2-bromopyridine (1.25 ml) at room temperature, and the resulting mixture was stirred at 150° C. for 16 hours. After cooling to room temperature, the reaction mixture was diluted with ethyl acetate, and the organic layer was washed with a saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate and evaporated in vacuo. The residue obtained was purified by chromatography on a silica gel column using a mixed solvent of ethyl acetate and hexane (1:2) as the eluent to afford the title compound (0.80 g, yield: 20%) as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07030138B2 |
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| Source dataset | uspto-grants-2006_04 |
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| ORD ID | ord-fb136cea15524a588eec33bf8a0ece06 |
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| Source note | uspto-grants-2006_04 |
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