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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 331669Generated: October 30, 2026

HCID 178472562, compound → HCID 178525818, compound

https://huagongshe.com/reaction/331669

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 178472562HCID 178472562—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
ProductHCID 178525818HCID 178525818—
ProductHCID 178525819HCID 178525819—

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of (S)-3-benzyloxy-2-[(S)-2-(3′-chloro-biphenyl-4-yl)-1-(1H-tetrazol-5-ylcarbamoyl)-ethylamino]-propionic acid ethyl ester (47 mg, 0.090 mmol) in EtOAc (1 mL) and EtOH (1 mL) was added 5% Pd—C (9.6 mg, 0.0045 mmol). H2 gas was loaded with a balloon and the reaction mixture was stirred at 50° C. for 6 hours. The reaction mixture was filtered through celite pad and the filtrate was concentrated. The residue was purified by reverse phase HPLC (Sunfire C-18 column, eluent: 0.1% TFA in H2O/CH3CN) to give (S)-2-[(S)-2-(3′-chloro-biphenyl-4-yl)-1-(1H-tetrazol-5-ylcarbamoyl)-ethylamino]-3-hydroxy-propionic acid and (S)-2-[(S)-2-biphenyl-4-yl-1-(1H-tetrazol-5-ylcarbamoyl)-ethylamino]-3-hydroxy-propionic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08877786B2
Source datasetuspto-grants-2014_11
ORD IDord-5dd961d016ed49e788a403ef5c31106e
Source noteuspto-grants-2014_11