HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → N-{2-[2-(1-Methylpiperidin-2-yl)ethyl]phenyl}pyridine-2-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Ethyl 2-pyridinecarboxylate | HCID 17307 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-(2-Aminophenethyl)-1-methylpiperidine | HCID 11085282 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | N-{2-[2-(1-Methylpiperidin-2-yl)ethyl]phenyl}pyridine-2-carboxamide | HCID 20560098 | — |
Reaction Steps
A solution of 2-(o-aminophenethyl)-1-methylpiperidine (8.0 g., 0.037 mole) and ethyl picolinate (5.5 g., 0.037 mole) in DMSO (20 ml.) is treated with NaH (57%) in oil (1.6 g., 0.037 mole) with intermittent cooling to moderate the resulting vigorous reaction. After 2 hr., the mixture is poured into 150 ml. of H2O and the product isolated according to the procedure of Example 25. Crystallization from isopropyl ether affords 5.9 (50%) of analytically pure 2'-[2-(1-methyl-2-piperidyl)ethyl]picolinanilide, m.p. 65.5°-67° C. (corr.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | USRE030811 |
| Source dataset | uspto-grants-1981_12 |
| ORD ID | ord-8abbfbe731224238bd813b942118e801 |
| Source note | uspto-grants-1981_12 |