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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2217231Generated: November 1, 2026

Iodoethane → HCID 69103003, compound

https://huagongshe.com/reaction/2217231

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantEthyl AcetateHCID 8857—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 69102420HCID 69102420—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 69103003HCID 69103003—
ProductHCID 69103067HCID 69103067—

Reaction Conditions

Temperature25 °C

Reaction Steps

3-Amino-6-(6-oxo-1,6-dihydro-3-pyridyl)-5-phenyl-2-pyrazinecarboxylic acid (154 mg) was dissolved in DMF(5 ml). To the solution were added EtI (86.1 mg) and t-BuOK (61.9 mg). The mixture was stirred at 20-30° C. for 2 hours. The reaction mixture was portioned EtOAc and water. The organic layer was separated. The aqueous layer was extracted with EtOAc. The combined organic solution was washed with brine and dried over MgSO4. Evaporation of solvent gave oily residue. The above residue was purified by chromatography on silica gel (EtOAc only-EtOAc:MeOH=95:5, v/v) to give ethyl 3-amino-6-(6-oxo-1,6-dihydro-3-pyridyl)-5-phenyl-2-pyrazinecarboxylate (84 mg) and ethyl 3-amino-6-(1-ethyl-6-oxo-1,6-dihydro-3-pyridyl)-5-phenyl-2-pyrazinecarboxylate (28 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07407961B2
Source datasetuspto-grants-2008_08
ORD IDord-f4deb702f0a34f2698485c3ab78e4352
Source noteuspto-grants-2008_08