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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 491809Generated: October 29, 2026

Potassium Iodide → HCID 178500409, compound

https://huagongshe.com/reaction/491809

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantMethyl 5-bromovalerateHCID 79557—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 178478721HCID 178478721—
SolventEthyl AcetateHCID 8857—
SolventDimethylacetamideHCID 31374—
ProductHCID 178500409HCID 178500409—

Reaction Conditions

Temperature100 °C

Reaction Steps

Trans-3-(4-aminocyclohexylcarbonylamino)-N-(5-chloropyridin-2-yl)benzofuran-2-carboxamide dihydrochloride (300 mg) obtained in Example 219 is suspended in N,N-dimethylacetamide (5 ml), and thereto are added methyl 5-bromovalerate (106 μl), N,N-diisopropylethylamine (537 μl), and potassium iodide (111 mg), and the mixture is stirred at 100° C. for 24 hours. Methyl 5-bromovalerate (106 μl), N,N-diisopropylethylamine (537 μl) and potassium iodide (111 mg) are further added thereto, and the mixture is stirred at 100° C. for 12 hours. The reaction solution is diluted with ethyl acetate, and washed successively with a saturated aqueous sodium hydrogen carbonate solution, water, a saturated brine, and dried over sodium sulfate. The solvent is evaporated under reduced pressure, and the resulting residue is purified by NH-silica gel column chromatography (eluent: n-hexane/ethyl acetate=1/1, then ethyl acetate) to give trans-3-[4-(4-methoxycarbonylbutylamino)cyclohexylcarbonylamino]-N-(5-chloropyridin-2-yl)-benzofuran-2-carboxamide (101 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07531537B2
Source datasetuspto-grants-2009_05
ORD IDord-a30d33ea7bee41a79dd0e566e7c2b8a0
Source noteuspto-grants-2009_05