10549-15-2

Usage

Uses

Used in Pharmaceutical Industry:
ALPHA-OXO-N-[(R)-1-PHENYLETHYL]PHENYLACETAMIDE is used as a potential analgesic and anti-inflammatory drug for its potential to alleviate pain and reduce inflammation. ALPHA-OXO-N-[(R)-1-PHENYLETHYL]PHENYLACETAMIDE's chiral nature, specifically the (R)-enantiomer, is of interest due to its pharmacological activity, making it a valuable target for the development of new medications to treat various conditions that involve pain and inflammation.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, ALPHA-OXO-N-[(R)-1-PHENYLETHYL]PHENYLACETAMIDE serves as a subject of study for understanding its structure-activity relationships and optimizing its pharmacological properties. This research can lead to the design of more effective and safer drugs based on its chemical structure.
Used in Drug Development:
ALPHA-OXO-N-[(R)-1-PHENYLETHYL]PHENYLACETAMIDE is utilized in drug development processes to create novel therapeutics. Its potential as an analgesic and anti-inflammatory agent is being explored, with the aim of bringing a new medication to market that could offer improved treatment options for patients suffering from pain and inflammatory conditions.

InChI:InChI=1/C16H15NO2/c1-12(13-8-4-2-5-9-13)17-16(19)15(18)14-10-6-3-7-11-14/h2-12H,1H3,(H,17,19)/t12-/m1/s1

Upstream product

• 25726-04-9 phenylglyoxylyl chloride 
• 3886-69-9 (R)-1-phenyl-ethyl-amine 
• 611-73-4 Benzoylformic acid 
• 98-86-2 acetophenone 
• 93-91-4 1-phenylbutan-1,3-dione 

Downstream Products

• 135339-46-7 (S)-α-cyano-α-fluoro-N-<(R)-1-phenylethyl>phenylacetamide 
• 135311-65-8 (R)-α-cyano-α-fluoro-N-<(R)-1-phenylethyl>phenylacetamide 
• 135311-75-0 α-cyano-N-<(ethoxycarbonyl)phenylmethyl>-α-fluorophenylacetamide 
• 142936-46-7 (R)-(+)-α-cyano-α-fluorophenylacetic acid 
• 135311-72-7 (S)-Cyano-fluoro-phenyl-acetic acid 2,2,2-trifluoro-1-phenyl-ethyl ester 
• 135311-70-5 (S)-Cyano-fluoro-phenyl-acetic acid 1,2,2-trimethyl-propyl ester 

Relevant academic research and scientific papers

Selective amidation by a photocatalyzed umpolung reaction

A metal-catalyzed organic transformation merged with another organophotocatalyst has been developed under mild conditions for production of α-ketoamides. CuI-catalyzed highly selective and rapid COCH2-amidation in the presence of electrophilic CαO bonds, which is synchronized by an eosin Y (EY)-photocatalyst, furnishes a wide range of labile α-ketoamides, unsymmetrical oxalamides and chiral analogues on the treatment of 1,3-dicarbonyls with amines, PhIO and LED light at room temperature. The current strategy opens up a new avenue to making photocatalysis a common synthetic tool for large-scale production in academia and industry.

A novel approach for the one-pot preparation of α-ketoamides by anodic oxidation

The direct oxidative synthesis of α-ketoamides via anodic oxidation was developed by using dioxygen as a reactant under mild conditions. This methodology has a broad substrate scope (aromatic amines, aliphatic amines and ammonium acetate) and opens up an interesting and attractive avenue for the synthesis of α-ketoamide derivatives.

Chemistry of Novel Compounds with Multifunctional Carbon Structure. 9. Molecular Design, Synthetic Studies, and NMR Investigation of Several Efficient Chiral Derivatizing Reagents which Give Very Large (19)F NMR Δδ Values in Enantiomeric Excess Determination

In order to develop efficient ee-determining reagents potentially superior to MTPA (1), some multifunctional compounds 2-5 were rationally designed.From NMR investigations of the analogous diastereomeric derivatives it was found that the chemical shift differences for each pair of diastereomers (Δδ values) for CFPA derivatives 5d-f were approximately five times greater in (19)F NMR spectra and two times greater in 1H NMR spectra than those of 1d-f.Synthesis of the optically pure CFPA, (-)-5a nd (+)-5a, was achieved by nitrosation of each diasteromer of the optically active N-(1-phenylethyl)amides, 5fM and 5fL, followed by thermal decomposition.Various derivatives were prepared by the condensation of 5b and 1b with alcohol and amine nucleophiles, and both ΔδF and ΔδH values were obtained for each compound.The CFPA derivatives 5d-m have proven to be significantly superior for ee determinations when compared to the corresponding MTPA derivatives 1d-m, particularly in compounds having remotely disposed chiral centers.