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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1628293Generated: October 30, 2026

Trifluoroacetic acid → HCID 67497288, compound

https://huagongshe.com/reaction/1628293

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 69620884HCID 69620884—
SolventDichloromethaneHCID 6344—
ProductHCID 67497288HCID 67497288—

Reaction Steps

To a 25 ml flask was added (S)-tert-butyl 1-oxo-3-phenyl-1-(6-(pyridin-4-yl)indolin-1-yl)propan-2-ylcarbamate 50.D (300 mg, 0.68 mmole) 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 was resuspended and the solvent was removed as before. This procedure was repeated one more time to give (S)-2-amino-3-phenyl-1-(6-(pyridin-4-yl)indolin-1-yl)propan-1-one 50.E of as a light yellow oil (300 mg, 21% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08785468B2
Source datasetuspto-grants-2014_07
ORD IDord-7fb468ec869844619e55653acb2b3741
Source noteuspto-grants-2014_07