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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1945030Generated: November 2, 2026

Trifluoroacetic acid → HCID 59607596, compound

https://huagongshe.com/reaction/1945030

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 59607757HCID 59607757—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59607596HCID 59607596—
ProductHCID 59607612HCID 59607612—

Reaction Steps

To a solution of (R)-3-[2-(tert-butoxycarbonyl-ethoxycarbonylmethyl-amino)-propionylamino]-4-(3′-chloro-biphenyl-4-yl)-butyric acid ethyl ester (290 mg, 0.504 mmol) in THF (3 ml) and MeOH (0.5 ml) at room temperature is added 2M NaOH (1.009 ml, 2.017 mmol). The reaction is stirred at room temperature over night. The mixture is concentrated to dryness and the crude i taken up in DCM (3.00 ml), to which is added TFA (3.89 ml, 50.4 mmol) and the mixture is stirred at room temperature for 2 hr. The reaction is concentrated for HPLC purification. Reverse phase HPLC [25 to 50% ACN—H2O (0.1% TFA) over 10 min by Sunfire C18 column] give (R)-3-[(S)-2-(Carboxymethyl-amino)-propionylamino]-4-(3′-chloro-biphenyl-4-yl)-butyric acid and (R)-3-[(R)-2-(Carboxymethyl-amino)-propionylamino]-4-(3′-chloro-biphenyl-4-yl)-butyric acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08394853B2
Source datasetuspto-grants-2013_03
ORD IDord-5d9e6558c7ea41e69313f8f3e9c60631
Source noteuspto-grants-2013_03