β-ANTHRONYL-β-PHENYL-PROPIONIC ACID AND ITS DERIVATIVES SYNTHESIS OF THE γ-ANTHRONYL-α-HYDRINDONE

1933 ◽  
Vol 8 (6) ◽  
pp. 600-615 ◽  
Author(s):  
Paul E. Gagnon ◽  
Lucien Gravel

Benzaldehyde and o-chlorbenzaldehyde were readily condensed with ethyl and methyl malonate, giving rise to unsaturated esters. The esters were condensed with anthrone in alcoholic solution in the presence of piperidine. Hydrolysis of the product with sulphuric acid yielded β-anthronyl-β-phenyl-propionic acid. The chloride of this acid was formed by the action of phosphorus pentachloride. Two tautomeric derivatives of γ-anthronyl-α-hydrindone result from the action of aluminium chloride on β-anthronyl-β-phenyl-propionyl chloride. No benzanthrone derivatives were formed.The action of bromine on the two tautomeric forms of γ-anthronyl-α-hydrindone gave rise to one monobromide only, and oxidation of the two tautomers yielded only anthraquinone and phthalic acid.The method of preparation of β-anthronyl-β-phenylpropionic acid has been improved and the following compounds have been described, as far as the authors are aware, for the first time: the dimethyl and diethyl esters of o-chlor-benzylidene - malonic acid and anthrone - o - chlorbenzylidene - malonic acid; anthrone - benzylidene - diethyl - malonate; β-anthronyl - β- (o - chlorphenyl) - propionic acid; the silver salt, chloride, amide, anilide, methyl and ethyl esters of β-anthronyl-β-phenyl-propionic acid; γ-anthronyl-α-hydrindone (enolic and ketonic forms); γ-anthronyl-β-brom-α-hydrindone; and the hydrazone hydrate, phenylhydrazone, oxime and semicarbazone of γ-anthronyl-α-hydrindone.

1980 ◽  
Vol 45 (2) ◽  
pp. 491-503 ◽  
Author(s):  
Karel Šindelář ◽  
Jiří Holubek ◽  
Emil Svátek ◽  
Miroslav Protiva

Alkylation of diethyl malonate with 2-(4-chlorophenylthio)benzyl chloride, the following hydrolysis and decarboxylation gave 3-[2-(4-chlorophenylthio)phenyl]propionic acid (IV); its chloride was cyclized in low yield by treatment with aluminium chloride to 4-(4-chlorophenylthio)indanone (V). The corresponding methylpiperazine derivative VIII was prepared viaintermediates VI and VII. A reaction of 3-(2-mercaptophenyl)propionic acid with 5-chloro-2-iodobenzoic acid and the following esterification resulted in the diester XVI which was cyclized by a Dieckmann reaction using sodium hydride in toluene to give ethyl 3-chloro-5-hydroxy-7H-dibenzo[b,g]thiocin-6-carboxylate (XVII). The acid hydrolysis afforded the ketone XVIII which was transformed via the intermediates XX and XXI to the title compound II. The product has a mild central depressant activity but it lacks the character of a neuroleptic agent.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Parisa Jahanbakhsh Bonab ◽  
Alireza Rastkar Ebrahimzadeh ◽  
Jaber Jahanbin Sardroodi

AbstractDeep eutectic solvents (DESs) have received much attention in modern green chemistry as inexpensive and easy to handle analogous ionic liquids. This work employed molecular dynamics techniques to investigate the structure and dynamics of a DES system composed of choline chloride and phenyl propionic acid as a hydrogen bond donor and acceptor, respectively. Dynamical parameters such as mean square displacement, liquid phase self-diffusion coefficient and viscosity are calculated at the pressure of 0.1 MPa and temperatures 293, 321 and 400 K. The system size effect on the self-diffusion coefficient of DES species was also examined. Structural parameters such as liquid phase densities, hydrogen bonds, molecular dipole moment of species, and radial and spatial distribution functions (RDF and SDF) were investigated. The viscosity of the studied system was compared with the experimental values recently reported in the literature. A good agreement was observed between simulated and experimental values. The electrostatic and van der Waals nonbonding interaction energies between species were also evaluated and interpreted in terms of temperature. These investigations could play a vital role in the future development of these designer solvents.


2017 ◽  
Vol 15 (19) ◽  
pp. 4218-4225 ◽  
Author(s):  
Arpita Paikar ◽  
Mintu Debnath ◽  
Debasish Podder ◽  
Supriya Sasmal ◽  
Debasish Haldar

The incorporation of a β-amino acid, namely 2-aminomethyl-3-(4-methoxy-phenyl)-propionic acid, inhibits amyloid-like fibril formation.


1991 ◽  
Vol 39 (9) ◽  
pp. 2323-2332 ◽  
Author(s):  
Youichiro NAITO ◽  
Tomokazu GOTO ◽  
Fumihiko AKAHOSHI ◽  
Shiniciro ONO ◽  
Haruko YOSHITOMI ◽  
...  

Author(s):  
Bahareh Mansoorian ◽  
Emilie Combet ◽  
Areej Alkhaldy ◽  
Ada L. Garcia ◽  
Christine Ann Edwards

Dietary fibre and polyphenols are both metabolised to short-chain fatty acids (SCFAs) and phenolic acids (PA) by the colonic microbiota. These may alter microbiota growth/diversity, but their interaction is not understood. Interactions between rutin and raftiline, ispaghula or pectin were investigated in human faecal batch cultures (healthy participants; 19–33 years, 4 males, 6 females, BMI 18.4–27.4) after a low (poly)phenol diet three days prior to study. Phenolic acids were measured by gas chromatography-mass spectrometry and SCFAs by gas chromatography-flame ionisation after 2, 4, 6, and 24 h. Rutin fermentation produced Phenyl acetic acid (PAA), 4-Hydroxy benzoic acid (4-OHBA), 3-Hydroxy phenyl acetic acid (3-OHPAA), 4-Hydroxy phenyl acetic acid (4-OHPAA), 3,4-Dihydroxy phenyl acetic acid (3,4-diOHPAA), 3-Hydroxy phenyl propionic acid (3-OHPPA), and 4-Hydroxy phenyl propionic acid (4-OHPPA). 3,4-DiOHPAA and 3-OHPAA were predominant at 6 h (1.9 ± 1.8 µg/mL, 2.9 ± 2.5 µg/mL, and 0.05 ± 0.0 µg/mL, respectively) and 24 h (5.5 ± 3.3 µg/mL, 3.1 ± 4.2 µg/mL, and 1.2 ± 1.6 µg/mL). Production of all PA except 3-OHPPA and 4-OHPPA was reduced by at least one fibre. Inhibition of PA was highest for rutin (8-fold, p < 0.01), then pectin (5-fold, p < 0.01), and ispaghula (2-fold, p = 0.03). Neither rutin nor quercetin had a detectable impact on SCFA production. These interactions should be considered when assessing dietary polyphenols and potential health benefits.


1973 ◽  
Vol 4 (48) ◽  
pp. no-no
Author(s):  
R. W. J. CARNEY ◽  
J. J. CHART ◽  
R. GOLDSTEIN ◽  
N. HOWIE ◽  
J. WOJTKUNSKI

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