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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantPotassium CarbonateHCID 11430—
Reactant6-amino-5-chloro-2-oxo-N-(4-piperidinylmethyl)-1,2-dihydro-3-pyridinecarboxamide dihydrochlorideHCID 22262609—
SolventDimethylformamideHCID 6228—
Product6-Amino-5-chloro-N-[(1-ethyl-4-piperidinyl)methyl]-2-oxo-1,2-dihydro-3-pyridinecarboxamideHCID 2226264449.1%

Reaction Conditions

Temperature60 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06979690B2
Source datasetuspto-grants-2005_12
ORD IDord-1a2e730f145440e69cc9ac4b321c54cc
Source noteuspto-grants-2005_12