Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | 4-Piperidinecarboxamide | HCID 3772 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Ethyl 6-chloronicotinate | HCID 2799611 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 31535351 | HCID 31535351 | — |
Reaction Steps
Ethyl-6-chloronicotinate (1.86 g, 10 mmol) and piperidine-4-carboxamide (1.54 g, 12 mmol) are dissolved in DMSO (7 ml). N,N-Diisopropylethylamine (2.1 ml, 12 mmol) is added and the reaction mixture is heated at 95° C. for 3 hours. Methanol (8 ml) is added as the reaction mixture cools to give a precipitate. The solid is collected, washed with water followed by diethyl ether, and dried in vacuo at 45° C. to yield the title compound as a white solid. MS (ES+) m/e 278 (MH+)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08114877B2 |
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| Source dataset | uspto-grants-2012_02 |
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| ORD ID | ord-6acccb1414224593912f1bed1a424689 |
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| Source note | uspto-grants-2012_02 |
|---|