6-(Bis-(2,2,2-trifluoroethyl)amino)-4-trifluoromethyl-1H-quinolin-2-one
[CAS# 328947-93-9]

Identification

• Classification: Pharmaceutical intermediate >> Heterocyclic compound intermediate >> Quinoline compound
• Name: 6-(Bis-(2,2,2-trifluoroethyl)amino)-4-trifluoromethyl-1H-quinolin-2-one
• Synonyms: LGD-2226
• Molecular Formula: C₁₄H₉F₉N₂O
• Molecular Weight: 392.22
• CAS Registry Number: 328947-93-9
• EC Number: 803-690-9
• SMILES: C1=CC2=C(C=C1N(CC(F)(F)F)CC(F)(F)F)C(=CC(=O)N2)C(F)(F)F

Properties

• Solubility: 0.7661 mg/L (25 ºC water)
• Density: 1.5±0.1 g/cm³, Calc.^*
• Index of Refraction: 1.463, Calc.^*
• Melting point: 152.96 ºC
• Boiling Point: 377.15 ºC, 364.4±42.0 ºC (760 mmHg), Calc.^*
• Flash Point: 174.2±27.9 ºC, Calc.^*

^* Calculated using Advanced Chemistry Development (ACD/Labs) Software.

Safety Data

• Hazard Symbols: GHS08 Warning
• Hazard Statements: H373
• Precautionary Statements: P260-P319-P501

Hazard Classification

Hazard	Class	Category Code	Hazard Statement
Specific target organ toxicity - repeated exposure	STOT RE	2	H373

Discovory and Applicatios

6-(Bis-(2,2,2-trifluoroethyl)amino)-4-trifluoromethyl-1H-quinolin-2-one is a notable compound in the field of medicinal chemistry, primarily due to its unique structure and potential biological activities. This quinoline derivative features multiple trifluoromethyl groups and a bis(trifluoroethyl) amino substituent, contributing to its chemical stability and lipophilicity, which are important for drug-like properties.

The discovery of this compound can be traced back to the growing interest in fluorinated organic compounds, particularly in the development of pharmaceuticals. Fluorine is known to enhance the metabolic stability and bioavailability of drugs, making fluorinated compounds an area of active research. The presence of the quinoline core in this structure adds to its significance, as quinolines are recognized for their diverse pharmacological profiles, including antimalarial, anticancer, and antimicrobial activities.

The synthesis of 6-(bis-(2,2,2-trifluoroethyl)amino)-4-trifluoromethyl-1H-quinolin-2-one typically involves several key steps. Initially, a suitable quinoline precursor is functionalized through various reactions, such as nucleophilic substitution or coupling reactions, to introduce the trifluoromethyl and bis(trifluoroethyl) amino groups. These synthetic routes are often optimized to enhance yield and purity, enabling researchers to obtain the target compound efficiently.

In terms of applications, the unique chemical structure of 6-(bis-(2,2,2-trifluoroethyl)amino)-4-trifluoromethyl-1H-quinolin-2-one positions it as a candidate for drug development. The trifluoromethyl groups can influence the compound's interaction with biological targets, potentially enhancing its efficacy and selectivity. Preliminary studies have indicated that compounds with similar structural motifs exhibit promising biological activities, making this compound a valuable addition to the medicinal chemistry toolbox.

Moreover, the compound’s potential as a building block for further chemical modifications is significant. The trifluoromethyl and bis(trifluoroethyl) amino groups can participate in various chemical reactions, allowing for the synthesis of a wide range of derivatives. This versatility is advantageous in the search for new therapeutic agents, as it enables the exploration of different substituents that may improve pharmacological properties.

Research into the biological activities of 6-(bis-(2,2,2-trifluoroethyl)amino)-4-trifluoromethyl-1H-quinolin-2-one is ongoing, with scientists investigating its potential effects on various biological pathways. The compound’s lipophilic nature may facilitate its penetration into biological membranes, enhancing its activity against targeted cells. As the field of medicinal chemistry continues to evolve, compounds like this one represent important milestones in the quest for novel therapeutics.

In summary, 6-(bis-(2,2,2-trifluoroethyl)amino)-4-trifluoromethyl-1H-quinolin-2-one is a fluorinated quinoline derivative with significant potential in medicinal chemistry. Its unique structural features and the presence of trifluoromethyl groups may enhance its biological activity and pharmacokinetic properties. Ongoing research will likely uncover further applications and lead to the development of new compounds based on this promising structure.