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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 548557Generated: October 29, 2026

(2-Methyl-4-{3-[3-(3-piperidin-1-yl-prop-1-ynyl)-5-(4-trifluoromethyl-phenylethynyl)-phenyl]-prop-2-ynyloxy}-phenoxy)-acetic acid methyl ester → (2-Methyl-4-{3-[3-(3-piperidin-1-yl-prop-1-ynyl)-5-(4-trifluoromethyl-phenylethynyl)-phenyl]-prop-2-ynyloxy}-phenoxy)-acetic acid

https://huagongshe.com/reaction/548557

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2-Methyl-4-{3-[3-(3-piperidin-1-yl-prop-1-ynyl)-5-(4-trifluoromethyl-phenylethynyl)-phenyl]-prop-2-ynyloxy}-phenoxy)-acetic acid methyl esterHCID 67158106—
SolventEthanolHCID 702—
SolventSodium HydroxideHCID 14798—
Product(2-Methyl-4-{3-[3-(3-piperidin-1-yl-prop-1-ynyl)-5-(4-trifluoromethyl-phenylethynyl)-phenyl]-prop-2-ynyloxy}-phenoxy)-acetic acidHCID 24752598—

Reaction Steps

A solution of (2-methyl-4-{3-[3-(3-piperidin-1-yl-prop-1-ynyl)-5-(4-trifluoromethylphenylethynyl)-phenyl]-prop-2-ynyloxy}-phenoxy)-acetic acid methyl ester (30 mg, 0.05 mmol) in ethanol (1 ml) and 1N NaOH (0.25 ml) was stirred at 75° C. for 30 min. The reaction mixture was evaporated and the residue dissolved in water (2 ml). Aqueous 1N HCl (0.25 ml) was added and the mixture was extracted with methylene chloride (2×10 ml). The combined organic phases were dried and evaporated to give the title compound in 25 mg (86%) yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07943612B2
Source datasetuspto-grants-2011_05
ORD IDord-09582a95c1674c6087c05d373ab33d15
Source noteuspto-grants-2011_05