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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1628203Generated: November 2, 2026

Trifluoroacetic acid → HCID 67497465, compound

https://huagongshe.com/reaction/1628203

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 70865441HCID 70865441—
SolventDichloromethaneHCID 6344—
ProductHCID 67497465HCID 6749746581.1%

Reaction Steps

To a 25 ml flask was added (S)-tert-butyl 1-oxo-3-phenyl-1-(3-(pyridin-4-yl)isoxazol-5-ylamino)propan-2-ylcarbamate 3.3B (160 mg, 0.40 mmoles), 10 ml of CH2Cl2, and 5 ml of TFA. The reaction was stirred at room temperature for 3 hour at which time the solvent was removed with a stream of nitrogen. The crude material was then partitioned between 200 ml of DCM and 100 ml of saturated sodium bicarbonate. The organic solvent was removed by rotary evaporation to give (S)-2-amino-3-phenyl-N-(3-(pyridin-4-yl)isoxazol-5-yl)propanamide 3.3.C as a light yellow solid (100 mg, 81% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08785468B2
Source datasetuspto-grants-2014_07
ORD IDord-30a40efa770e45c0a8cdd070fc1727a9
Source noteuspto-grants-2014_07