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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1877177Generated: November 2, 2026

Sodium Iodide → HCID 59529438, compound

https://huagongshe.com/reaction/1877177

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantSodium CarbonateHCID 10340—
ReactantEthyl 3-{[(4-aminophenyl)carbonyl](methyl)amino}propanoateHCID 46941342—
ReactantHCID 68513235HCID 68513235—
SolventWaterHCID 962—
SolventDimethylacetamideHCID 31374—
ProductHCID 59529438HCID 5952943854%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 3-{4-[cyclohexyl(hydroxy)methyl]-5-methylfuran-2-yl}benzamide (0.6 g), ethyl 3-{[(4-aminophenyl)carbonyl](methyl)amino}propanoate (0.7 g), sodium carbonate (0.3 g) and sodium iodide (0.6 g) in N,N-dimethylacetamide (20 mL) was stirred at 80° C. for 8 hr. The reaction mixture was poured into water, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over magnesium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel chromatography (50% ethyl acetate/hexane to 100% ethyl acetate/hexane). To the residue were added ethanol (3 mL), tetrahydrofuran (3 mL) and 1N lithium hydroxide (2.5 mL), and the mixture was stirred at room temperature for 1 hr. The solvent was evaporated under reduced pressure, and water (10 mL) was added. The mixture was neutralized with 1N hydrochloric acid under ice-cooling, and stirred for 1 hr. The resulting precipitate was collected by filtration and dried to give the title compound (527 mg, 54%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08309580B2
Source datasetuspto-grants-2012_11
ORD IDord-9f0def8efcef4e38899f73f9f7932fe2
Source noteuspto-grants-2012_11