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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 353478Generated: October 31, 2026

Trifluoroacetic acid → HCID 23514103, compound

https://huagongshe.com/reaction/353478

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 23513969HCID 23513969—
SolventDichloromethaneHCID 6344—
ProductHCID 23514103HCID 2351410360.4%

Reaction Steps

Trifluoroacetic acid (0.1 ml) is added to a stirred solution of tert-butyl 2-{[(1-(4-chlorobenzyl)-3-{oxo[(5-oxo-2,5-dihydro-3-furanyl)amino]acetyl}-1H-indol-4-yl)carbonyl]amino}ethylcarbamate of Example 9 (50 mg) in CH2Cl2 (1 ml). After stirring at room temperature for 3 h the solvent is removed by roto-evaporation and the residue is taken up with water, adjusting the pH at about 8-9 with 1N NaOH. The precipitate is collected by filtration and thoroughly washed to give N-(2-aminoethyl)-1-(4-chlorobenzyl)-3-{oxo[(5-oxo-2,5-dihydro-3-furanyl)amino]acetyl}-1H-indole-4-carboxamide (25 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06753342B2
Source datasetuspto-grants-2004_06
ORD IDord-278060cb51f54eccbd15fc11362e5eff
Source noteuspto-grants-2004_06