Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | 6-Fluoropyridin-2-amine | HCID 2761399 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 18771896 | HCID 18771896 | 94.9% |
Reaction Steps
A suspension of 6-fluoropyridin-2-amine (500 mg, 4.4 mmol), piperidine (1.4 mL, 14.1 mmol) in water (0.5 mL) was heated to 205° C. in a microwave oven for 30 minutes. The reaction mixture was purified by chromatography (silica gel, 200-300 mesh, petroleum ether:ethyl acetate=3:1) to give 6-(piperidin-1-yl)pyridin-2-amine (740 mg, 94%) as a light yellow oil. LC-MS: [M+H]+, 178.1, tR=0.974 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09169259B2 |
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| Source dataset | uspto-grants-2015_10 |
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| ORD ID | ord-27f173cfa60244c1ae21cb02b889cd4a |
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| Source note | uspto-grants-2015_10 |
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