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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1877180Generated: November 2, 2026

Sodium Iodide → HCID 59529564, compound

https://huagongshe.com/reaction/1877180

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantSodium CarbonateHCID 10340—
ReactantEthyl 3-{[(4-aminophenyl)carbonyl](methyl)amino}propanoateHCID 46941342—
ReactantHCID 68512524HCID 68512524—
SolventWaterHCID 962—
SolventDimethylacetamideHCID 31374—
ProductHCID 59529564HCID 5952956433%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 3-{4-[chloro(cyclohexyl)methyl]-5-methylfuran-2-yl}-6-methylpyridazine (107 mg), ethyl 3-{[(4-aminophenyl)carbonyl](methyl)amino}propanoate (175 mg), sodium carbonate (74 mg) and sodium iodide (210 mg) in N,N-dimethylacetamide (5 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 (30% ethyl acetate/hexane to 100% ethyl acetate/hexane). To the residue were added ethanol (2 mL), tetrahydrofuran (2 mL) and 1N lithium hydroxide (0.3 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 (56 mg, 33%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08309580B2
Source datasetuspto-grants-2012_11
ORD IDord-a2d656a5b6f242c48fe2c8ea5603e816
Source noteuspto-grants-2012_11