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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1371286Generated: November 1, 2026

Trifluoroacetic acid → HCID 178446022, compound

https://huagongshe.com/reaction/1371286

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantAnisoleHCID 7519—
Reactant(3S)-3-[N-((1-Naphthylamino)Acetyl)Leucinyl]Amino-4-Oxobutanoic Acid tert-Butyl Ester SemicarbazoneHCID 86585452—
SolventDichloromethaneHCID 6344—
ProductHCID 178446022HCID 17844602298.4%

Reaction Steps

To a solution of (3S)-3-[N-((1-naphthylamino)acetyl)leucinyl]amino-4-oxobutanoic acid tert-butyl ester semicarbazone (0.201 g, 0.38 mmol) in CH2Cl2(2.0 mL)-anisole(0.5 mL) at room temperature under nitrogen was added trifluoroacetic acid (2.0 mL). The resulting solution was stirred at room temperature for 5 hrs, evaporated to dryness and chased with CH2Cl2 and toluene-CH2Cl2 (1:1). The resulting solid was triturated with CHCl2-Et2O to give the title compound (0.176 g, 98%) as a pale gray solid. TLC(EtOAc-pyridine-AcOH-H2O; 60:20:5:10) Rf=0.45.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07157430B2
Source datasetuspto-grants-2007_01
ORD IDord-0099f33ab37849df843532d42cabbbbe
Source noteuspto-grants-2007_01