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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2304349Generated: November 1, 2026

Trifluoroacetic acid → HCID 54159988, compound

https://huagongshe.com/reaction/2304349

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 54572064HCID 54572064—
SolventDichloromethaneHCID 6344—
ProductHCID 54159988HCID 5415998862.4%

Reaction Steps

Trifluoroacetic acid (3.0 mL) was added to 150 mg of (2-{2(S)-[(1-amino-isoquinolin-6-ylmethyl)-carbamoyl]-pyrrolidin-1-yl}-2-oxo-1(R)-phenyl-ethyl)-carbamic acid tert-butyl ester (prepared according to the procedures described in example 110) in 3.0 mL dichloromethane. Stirring was continued for 2 h at ambient temperature. The solvent was removed i.vac, the residue was dissolved in methanol and applied to a reversed-phase chromatography column (lenght 100 mm, diameter 14 mm; Merck Lichroprep RP-18, 15-25μ). Elution was started with 25 mL of methanol/water containing 0.3% acetic acid (10:90), then a linear gradient to pure methanol over a period of 75 mL was applied followed by 50 mL of pure methanol. Fractions of 5 mL each were sampled, The solvent was removed to give 75 mg (62%) of the title compound. MS: 404.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06432955B1
Source datasetuspto-grants-2002_08
ORD IDord-5f5843fa01074d93bce44bd83d4efa74
Source noteuspto-grants-2002_08