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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 418069Generated: October 30, 2026

Hydrochloric Acid → 4-{2-(2-Carboxy-ethyl)-3-[6-(3-methanesulfonyl-5-thiazol-4-yl-phenoxy)-hexyl]-phenoxy}-butyric Acid

https://huagongshe.com/reaction/418069

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant4-{2-(2-Ethoxycarbonyl-ethyl)-3-[6-(3-methanesulfonyl-5-thiazol-4-yl-phenoxy)-hexyl]-phenoxy}-butyric Acid Ethyl EsterHCID 57863124—
SolventEthanolHCID 702—
SolventSodium HydroxideHCID 14798—
Product4-{2-(2-Carboxy-ethyl)-3-[6-(3-methanesulfonyl-5-thiazol-4-yl-phenoxy)-hexyl]-phenoxy}-butyric AcidHCID 5786307546.5%

Reaction Conditions

Temperature70 °C

Reaction Steps

To a solution of 4-{2-(2-ethoxycarbonyl-ethyl)-3-[6-(3-methanesulfonyl-5-thiazol-4-yl-phenoxy)-hexyl]-phenoxy}-butyric acid ethyl ester (280 mg, 0.434 mmol) in EtOH (20 mL), 3N NaOH (1 mL) was added and heated at 70° C. for 2 h. The reaction was acidified with 3N HCl (1.1 mL). Concentration under reduced pressure gave an oil. Preparative HPLC provided title compound (119 mg, 46% yield). LC/MS indicated a purity of 92% as measured by UV 214 nM. HR-ES(+): calculated for C29H36NO8S2 (M+H)1+ 590.1877, found 590.1876.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08093253B2
Source datasetuspto-grants-2012_01
ORD IDord-e987a87bb0d14e17abae07e987c652b5
Source noteuspto-grants-2012_01