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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1919920Generated: November 1, 2026

Trifluoroacetic acid → HCID 24753858, compound

https://huagongshe.com/reaction/1919920

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 69483281HCID 69483281—
SolventDichloromethaneHCID 6344—
ProductHCID 24753858HCID 24753858—

Reaction Steps

To a solution of the trifluoroacetic acid salt of tert-butyl [2-[(4-{2-anilino-1-[(dimethylamino)methyl]-2-oxoethyl}benzoyl)amino]-4-(3-thienyl)phenyl]carbamate (374 mg, 0.54 mmol) in CH2Cl2 (8 mL) was added trifluoroacetic acid (2 mL), and the reaction was stirred at room temperature for 1 h. Concentration yielded a yellow residue that was purified by reverse phase HPLC (10-70% MeCN/water). The resulting solid was dissolved in CH2Cl2 (with a small amount of MeOH), neutralized with sat. NaHCO3, washed with brine, dried (MgSO4), and evaporated to yield N-[2-amino-5-(3-thienyl)phenyl]-4-{2-anilino-1-[(dimethylamino)methyl]-2-oxoethyl}benzamide as an off-white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08168658B2
Source datasetuspto-grants-2012_05
ORD IDord-554389df808d4f5e863b8a824a826c53
Source noteuspto-grants-2012_05