Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Chloropyridine | HCID 7977 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 18-Crown-6 | HCID 28557 | — |
| Reactant | HCID 22675416 | HCID 22675416 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 22675455 | HCID 22675455 | 268.5% |
Reaction Steps
218 mg of the compound obtained in Example 16a, 115 mg of 2-chloropyridine, 200 mg of KOH and 50 mg of 18-crown-6-ether were added to 15 ml of DMSO and the mixture was heated to 150° C. for 8 hours. The reaction mixture was cooled, then added with water and extracted with ethyl acetate. The extract was dried over sodium sulfate, and the solvent was evaporated under reduced pressure. The resulting residue was purified by silica gel column chromatography (ethyl acetate) to obtain 150 mg of the title compound (yield: 51%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06787561B1 |
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| Source dataset | uspto-grants-2004_09 |
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| ORD ID | ord-900643aa4fe64513b5acb00af66df358 |
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| Source note | uspto-grants-2004_09 |
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