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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2091229Generated: November 1, 2026

Ammonium Chloride → Ethyl 3-{[(4-{[1-(5-methoxy-3-methyl-1-benzofuran-2-yl)heptyl]amino}phenyl)carbonyl]amino}propanoate

https://huagongshe.com/reaction/2091229

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactantbeta-Alanine, ethyl ester, hydrochlorideHCID 458475—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant1-Hydroxybenzotriazole hydrateHCID 2796029—
Reactant4-{[1-(5-Methoxy-3-methyl-1-benzofuran-2-yl)heptyl]amino}benzoic acidHCID 66778801—
SolventDimethylformamideHCID 6228—
SolventTriethylamineHCID 8471—
ProductEthyl 3-{[(4-{[1-(5-methoxy-3-methyl-1-benzofuran-2-yl)heptyl]amino}phenyl)carbonyl]amino}propanoateHCID 6677780885.3%

Reaction Steps

To a mixture of 4-{[1-(5-methoxy-3-methyl-1-benzofuran-2-yl)heptyl]amino}benzoic acid (300 mg) synthesized above, β-alanine ethyl ester hydrochloride (175 mg), 1-hydroxybenzotriazole monohydrate (175 mg), triethylamine (318 μL) and N,N-dimethylformamide (10 mL) was added 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (219 mg), and the mixture was stirred overnight at room temperature. Saturated aqueous ammonium chloride solution was added to quench the reaction, and the reaction mixture was extracted with ethyl acetate. The extract was washed with saturated aqueous sodium hydrogen carbonate solution and saturated brine, dried over magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (30-100% ethyl acetate/hexane) to give the title object compound (320 mg, 85%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08436043B2
Source datasetuspto-grants-2013_05
ORD IDord-f6cee4fae6ae4df795b86ac14b11f060
Source noteuspto-grants-2013_05