Ammonium Chloride → HCID 66777420, compound

Participants

Reaction Steps

To a mixture of 4-{[cyclohexyl(6-methoxy-1-methyl-1H-benzimidazol-2-yl)methyl]amino}benzoic acid (270 mg) synthesized above, β-alanine ethyl ester hydrochloride (158 mg), 1-hydroxybenzotriazole monohydrate (158 mg), triethylamine (287 μL) and N,N-dimethylformamide (10 mL) was added 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (198 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 1N hydrochloric acid, 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 (60-100% ethyl acetate/hexane) to give the title object compound (151 mg, 45%) as a pale-yellow oil.

Provenance & Evidence