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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 423214Generated: October 30, 2026

Boric Acid → 2-Ethoxy-4-(3-((S)-3-methy-1-(2-piperidin-1-yl-phenyl)-butylamino)-2-oxo-propyl)-benzoic acid ethyl ester

https://huagongshe.com/reaction/423214

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoric AcidHCID 7628—
Reactant3-Ethoxy-4-ethoxycarbonylphenylacetic acidHCID 10131212—
Reactant3-Methyl-1-(2-piperidinophenyl)-1-butylamine, (S)-HCID 10514609—
SolventTolueneHCID 1140—
Product2-Ethoxy-4-(3-((S)-3-methy-1-(2-piperidin-1-yl-phenyl)-butylamino)-2-oxo-propyl)-benzoic acid ethyl esterHCID 1064841973.3%

Reaction Conditions

Temperature27.5 °C

Reaction Steps

In a round bottom flask fitted with a dean stark condenser, (S)-3-methyl-1-(2-piperidinophenyl)-1-butylamine (10 g, 0.0406 mol) was dissolved in toluene (100 ml), followed by the addition of 3-ethoxy-4-ethoxycarbonyl phenyl acetic acid (10.26 g, 0.0407 mol) and boric acid (0.26 g, 0.0042 mol). The reaction mixture was refluxed for 16-18 hours. The resulting mass was then cooled to 25-30° C. followed by filtration. The filtrate was washed with water and 1.0% sodium bicarbonate solution followed by complete distillation of toluene and the resulting residue was stirred with hexane (50 ml) for 1 hour. The precipitated solid was filtered and washed with hexane (10 ml). The wet product was dried at 50-55° C. under vacuum for 4-6 hours to produce Ethyl (S)-2-ethoxy-4-[N-(1-(2-piperidino-phenyl)-3-methyl-1-butyl)-aminocarbonyl methyl]-benzoate (Yield=73.3%; HPLC Purity: 99.50%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08101769B2
Source datasetuspto-grants-2012_01
ORD IDord-22778ac9720749c5aa3d48fdb7d40014
Source noteuspto-grants-2012_01