scholarly journals Synthesis ofN-(5-(Substitutedphenyl)-4,5-dihydro-1H-pyrazol-3-yl)-4H-1,2,4-triazol-4-amine from 4-Amino-4H-1,2,4-triazole

2011 ◽  
Vol 8 (3) ◽  
pp. 1180-1185
Author(s):  
Ashvin D. Panchal ◽  
Pravin M. Patel
Keyword(s):  
Thin Layer ◽  
Hydrazine Hydrate ◽  
Thin Layer Chromatography ◽  
Aromatic Aldehyde ◽  
Acetyl Chloride ◽  
Spectroscopic Studies ◽  
H Nmr ◽  
Ir Spectroscopic ◽  
Layer Chromatography

N-(4H-1,2,4-Triazol-4-yl)acetamide (2) were prepared by reaction of 4-amino-4H-1,2,4-triazole (1) with acetyl chloride in dry benzene. It has been reacted with various aromatic aldehyde to afford 3-(substitutedphenyl)-N-(4H-1,2,4-triazol-4-yl)acrylamide (3a-e). The synthesis ofN-(5-substitutedphenyl)-4,5-dihydro-1H-pyrazol-3-yl)-4H-1,2,4-triazol-4-amine (4a-e) is achieved by the cyclisation of3a-ewith hydrazine hydrate in ethanol. The structures of synthesized compounds were characterized by1H NMR and IR spectroscopic studies. The purity of the compounds was checked by thin layer chromatography.

scholarly journals Synthesis and Antimicrobial Activity of (2-Methoxy/2-Amino)-6-{4'-[(4'''-Chlorophenyl) (Phenyl) Methyl Amino] Phenyl}-4-Aryl Nicotinonitrile

2015 ◽  
Vol 49 ◽  
pp. 99-103
Author(s):  
J.V. Guna ◽  
V.N. Bhadani ◽  
H.D. Purohit ◽  
Dipak M. Purohit
Keyword(s):  
Antimicrobial Activity ◽  
Thin Layer ◽  
Thin Layer Chromatography ◽  
Spectral Data ◽  
Elemental Analysis ◽  
Mass Spectral Data ◽  
Mass Spectral ◽  
H Nmr ◽  
Bacteria And Fungi ◽  
Layer Chromatography

2- Methoxy – 6 - {4' - [(4'''- Chlorophenyl) (phenyl) methyl amino] phenyl} - 4 - aryl nicotinonitrile (3a-3l) and 2-Amino-6-{4'-[(4'''-Chlorophenyl)(phenyl)methyl amino]phenyl}-4-aryl nicotinonitrile (4a-4l) have been synthesized. The products have been assayed for their antimicrobial activity against Gram +ve, Gram -ve bacteria and fungi. The structure of the products has been elucidated by IR, 1H-NMR, mass spectral data, elemental analysis and thin layer chromatography.

scholarly journals Phytochemical Analysis and Traditional uses of two locally available Ficus species (beneghalensis and sycomorus)

2021 ◽  
pp. 155-162
Author(s):  
Sulieman Ahmed Gasim El Said ◽  
Hatil Hashim EL-Kamali ◽  
Yousra Omer EL-Desogi
Keyword(s):  
Phenolic Compounds ◽  
Thin Layer ◽  
Traditional Medicine ◽  
Thin Layer Chromatography ◽  
Therapeutic Agent ◽  
Spectroscopic Studies ◽  
Phytochemical Analysis ◽  
Chemical Reagent ◽  
Chemical Basis ◽  
Layer Chromatography

Two Ficus species that are commonly used in Sudanese Traditional Medicine for the management of various ailments were screened for their phytochemical groups using chemical reagent and Thin Layer Chromatography. Qualitative phytochemical tests were used to detect the presence of flavonoids, saponins, tannins, alkaloids, phenolic compounds and anthraquinones. Six compounds from F. benegalensis and seven from F. sycomorus quenching were reported from the various parts of these two plants. However , more number of compounds were found in the leaves. The data generated from this study have provided the chemical basis for wide use of F. sycomorus as therapeutic agent for treating various ailments. However, there is need to further carry out advanced hyphenated spectroscopic studies in order to elucidate the structure of these compounds. Furthermore, this data may be handy in probing of biochemistry of this plant in the future.

α-Aminoacyl derivatives of α,ω-diaminopoly(oxyethylene)

1987 ◽  
Vol 52 (8) ◽  
pp. 1922-1927
Author(s):  
Bohumil Masař ◽  
Pavel Schmidt ◽  
Hana Pivcová ◽  
Pavel Čefelín
Keyword(s):  
Amino Acids ◽  
Nmr Spectroscopy ◽  
Thin Layer ◽  
Thin Layer Chromatography ◽  
Trifluoroacetic Acid ◽  
Complete Removal ◽  
Protective Group ◽  
H Nmr ◽  
Layer Chromatography ◽  
Derivatives Of

By reacting p-nitrophenyl esters of L-α-amino acids with α-(3-aminopropyl)-ω-(aminomethyl)-poly(oxyethylene), diamides having the structure [X-NHCH(R)CONH]2Mx' were prepared, X being the protective group Boc or Z, R being residues of glutamic and aspartic acid, phenylalanine and tyrosine, and Mx' being the poly(oxyethylene) chain with the (-CH2)3- and -CH2- endgroups. The diamides were characterized by IR and 1H NMR spectroscopy and thin-layer chromatography. After complete removal of tert-butyloxycarbonyl groups from diamides (X = Boc), deprotected α-aminoacyl derivatives were characterized as trifluoroacetic acid salts.

Thin-Layer Chromatography

1965 ◽  
Author(s):  
H. R. Bolliger ◽  
M. Brenner ◽  
H. Gänshirt ◽  
Helmut K. Mangold ◽  
H. Seiler ◽  
...  
Keyword(s):  
Thin Layer ◽  
Thin Layer Chromatography ◽  
Layer Chromatography

THE LESS-POLAR METABOLITES PRODUCED BY INCUBATION OF TESTOSTERONE-4-14C WITH RAT AND BOVINE BRAIN

1969 ◽  
Vol 61 (4) ◽  
pp. 641-648 ◽  
Author(s):  
Leon J. Sholiton ◽  
Emile E. Werk
Keyword(s):  
Thin Layer ◽  
Thin Layer Chromatography ◽  
Paper Chromatography ◽  
Specific Activity ◽  
Bovine Brain ◽  
Polar Fraction ◽  
End Products ◽  
Polar Metabolites ◽  
Layer Chromatography ◽  
Constant Specific Activity

ABSTRACT Rat and bovine brain have been incubated with testosterone-4-14C under standard conditions. With use of paper chromatography, the extracted metabolites were noted to fall into less-polar, iso-polar, and more polar fractions. The components of the less-polar fraction were separated by acetylation and thin-layer chromatography and the major end-products identified by recrystallization to constant specific activity or constant 3H/14C ratios. Androst-4-enedione and 5α-dihydrotestosterone were formed consistently under the conditions utilized. Trace amounts of other less-polar metabolites were noted occasionally.

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