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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 563607Generated: October 30, 2026

Hydrochloric Acid → 2-{2'-[(Acetyl-ethyl-amino)-methyl]-6-methoxy-4'-trifluoromethyl-biphenyl-3-yl}-2-methyl-propionic acid

https://huagongshe.com/reaction/563607

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDichloromethaneHCID 6344—
ReactantSodium HydroxideHCID 14798—
Reactant2-{2'-[(Acetyl-ethyl-amino)-methyl]-6-methoxy-4'-trifluoromethyl-biphenyl-3-yl}-2-methyl-propionic acid ethyl esterHCID 66607629—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
Product2-{2'-[(Acetyl-ethyl-amino)-methyl]-6-methoxy-4'-trifluoromethyl-biphenyl-3-yl}-2-methyl-propionic acidHCID 54673219—

Reaction Conditions

Temperature50 °C

Reaction Steps

To 2-{2′-[(acetyl-ethyl-amino)-methyl]-6-methoxy-4′-trifluoromethyl-biphenyl-3-yl}-2-methyl-propionic acid ethyl ester (0.290 g, 0.63 mmol) in THF (2.6 mL) and EtOH (2 mL) was added 1N aqueous NaOH (1.9 mL), and the reaction was stirred at 50° C. overnight. Analytical LCMS indicated that starting material was still present, so additional 1N aqueous NaOH (1 mL) was added, and the reaction was stirred at 70° C. for 2 hours. Additional 1N aqueous NaOH (1 mL) was added, and the reaction was stirred for another 6 hours. The mixture was worked-up with CH2Cl2 and 1N aqueous HCl, and the organic layer was dried over Na2SO4, decanted, and concentrated. The residue was purified by preparative HPLC to give the title compound. M+H is 438.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08067445B2
Source datasetuspto-grants-2011_11
ORD IDord-9ed8e40f60a3401ba0d81312d6ec1402
Source noteuspto-grants-2011_11