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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1628311Generated: November 1, 2026

Trifluoroacetic acid → HCID 67496285, compound

https://huagongshe.com/reaction/1628311

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 69620934HCID 69620934—
SolventDichloromethaneHCID 6344—
ProductHCID 67496285HCID 6749628582%

Reaction Steps

To a 20 ml vial was added crude (S)-tert-butyl 1-(4-carbamoyl-6-(pyridin-4-yl)indolin-1-yl)-1-oxo-3-phenylpropan-2-ylcarbamate 60.B (75 mg, 0.1 mmole), 20 ml of DCM and 10 ml of TFA. The reaction was stirred at room temperature for 12 hours at which time the crude was partitioned between 600 ml DCM and 100 ml saturated sodium carbonate. The organic layer was extracted once more with 100 ml of water, the organic layer dried with sodium sulfate and the solvent removed to give (S)-1-(2-amino-3-phenylpropanoyl)-6-(pyridin-4-yl)indoline-4-carboxamide 60.0 as an off white solid. (49 mg, 82% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08785468B2
Source datasetuspto-grants-2014_07
ORD IDord-d0f67f0815cf426686312db1c69c13b8
Source noteuspto-grants-2014_07