Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Chlorosuccinimide | HCID 31398 | — |
| Reactant | HCID 66994464 | HCID 66994464 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 67485692 | HCID 67485692 | 42.2% |
Reaction Steps
To a solution of 4-(2-aminopyridin-3-yloxy)benzonitrile (5.6 g, 26.5 mmol) in DMF (100 mL) was added N-chlorosuccinimide (4.25 g, 31.8 mmol) and stirred at 80° C. for 14 h. The reaction mixture was cooled to ambient temperature and poured into water (100 mL). The aqueous suspension was extracted with EtOAc and the combined organic layers were washed with water. The organic phase was dried (MgSO4), filtered, and concentrated in vacuo. The residue was purified on silica gel (20% EtOAc/hexanes) and triturated with methanol to afford 4-(2-amino-5-chloropyridin-3-yloxy)benzonitrile (2.75 g, 42.2% yield) as a bright yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08362037B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-a5cfd2b7963e49ff84b59f5660c79c9e |
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| Source note | uspto-grants-2013_01 |
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