HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 489784Generated: October 30, 2026
Iodoethane → 6-Amino-5-chloro-N-[(1-ethyl-4-piperidinyl)methyl]-2-oxo-1,2-dihydro-3-pyridinecarboxamide
https://huagongshe.com/reaction/489784
Participants
| Role | Name | HCID | Charge |
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| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 6-amino-5-chloro-2-oxo-N-(4-piperidinylmethyl)-1,2-dihydro-3-pyridinecarboxamide dihydrochloride | HCID 22262609 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 6-Amino-5-chloro-N-[(1-ethyl-4-piperidinyl)methyl]-2-oxo-1,2-dihydro-3-pyridinecarboxamide | HCID 22262644 | 49.1% |
Reaction Steps
A mixture of 6-amino-5-chloro-2-oxo-N-(4-piperidinylmethyl)-1,2-dihydro-3-pyridinecarboxamide dihydrochloride (step 2, 100 mg, 0.28 mmol), iodoethane (49 mg, 0.31 mmol) and potassium carbonate (172 mg, 1.25 mmol) in N,N-dimethylformamide (6 ml) was stirred at 60° C. for 15 h. After cooling to room temperature, the solvent was removed in vacuo. The residue was suspended in tetrahydrofuran (50 ml), and the solution was filtered through a pad of Celite. The filtrate was concentrated in vacuo, and the obtained residue was chromatographed on a column of aminopropyl silica gel eluting with methanol/dichloromethane (1:2.5) to give 43 mg (49%) of the title compound as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06979690B2 |
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| Source dataset | uspto-grants-2005_12 |
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| ORD ID | ord-1a2e730f145440e69cc9ac4b321c54cc |
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| Source note | uspto-grants-2005_12 |
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