Acetylene derivatives Part 128. Heterocyclic compounds. XXIII. Action of primary aromatic amines and ?-aminopyridine on vinyl allyl ketones. Synthesis of aryl-substituted ?-piperidones and 1-(?-pyridyl)-4-piperidones

1952 ◽  
Vol 1 (6) ◽  
pp. 923-932 ◽  
Author(s):  
I. N. Nazarov ◽  
S. G. Matsoyan ◽  
V. A. Rudenko
Keyword(s):  
Aromatic Amines ◽  
Heterocyclic Compounds ◽  
Primary Aromatic Amines ◽  
Acetylene Derivatives

scholarly journals A New Route for the Synthesis of Quinazolinones

2012 ◽  
Vol 12 ◽  
pp. 133-138 ◽  
Author(s):  
AD Mishra
Keyword(s):  
Aromatic Amines ◽  
Heterocyclic Compounds ◽  
Microbial Activities ◽  
Anti Cancer ◽  
Primary Aromatic Amines ◽  
Acidic Alumina ◽  
Microwave Reactions ◽  
Antibacterial And Antifungal ◽  
Quinazolinone Derivatives ◽  
Anti Hiv

Quinazolinone derivatives are highly bioactive heterocyclic compounds with wider range of microbial activities such as anti-malarial, anti-cancer, anti-inflammatory, anti-hypertensive, anti-convulsant, anti-HIV, etc. Solid supported microwave synthesis of some 3-substituted-4-(2H)-quinazolinones has been carried out by the reaction of anthranilic acid, formaldehyde and primary aromatic amines. The usage of hazardous reagents and organic solvents has been avoided. The reactions were conducted in presence of acidic alumina where formaldehyde entered into cycloaddition to yield the quinazolinone derivatives. The reactions completed within 2-4 minutes with 82-94% of yields in microwave reactions while it took 5-7 hours for completion affording only 56-68% of the yields in conventional reactions. The synthesized quinazolinone derivatives showed moderate to promising antibacterial and antifungal activities.DOI: http://dx.doi.org/10.3126/njst.v12i0.6491 Nepal Journal of Science and Technology 12 (2011) 133-138 

scholarly journals Synthesis and characterization Some of heterocyclic compounds from Nitrogen derivative

2019 ◽  
Vol 10 (4) ◽  
pp. 3186-3196
Author(s):  
Sarah Mohammed Abed ◽  
Hasan Thamer Ghanem
Keyword(s):  
Schiff Base ◽  
Aromatic Amines ◽  
Heterocyclic Compounds ◽  
Condensation Reaction ◽  
Synthesis And Characterization ◽  
Second Step ◽  
Azo Compound ◽  
Nitrogen Derivative ◽  
Amino Phenol ◽  
Primary Aromatic Amines

This paper involves the synthesis of new oxazepine derivatives by multi-reaction steps. The first step synthesis azo derivative from 2-naphthol with 3-aminoacetophenone. The second step was the condensation reaction between ketone group of the azo compound and different primary aromatic amines (4-amino phenol, 3-nitro aniline and 4-methyl aniline) to yiled new azo Schiff base compounds (S1-S3) respectively. In the final step, Oxazepine compounds (L1-L3)and (L4-L6)were prepared from reaction imine compounds (S1-S3) with maleic and phthalic anhydride in toluene as solvent. All these derivatives were characterized by melting point, FTIR, HNMR and 13CNMR.

Catalyst- and solvent-free Csp2-H functionalization of 4-hydroxycoumarins via C-3 dehydrogenative aza-coupling under ball-milling

2021 ◽  
Author(s):  
Goutam Brahmachari ◽  
Indrajit Karmakar ◽  
Pintu Karmakar
Keyword(s):  
Ball Milling ◽  
Aromatic Amines ◽  
Solvent Free ◽  
One Pot ◽  
Biologically Relevant ◽  
Tert Butyl ◽  
Three Component Reaction ◽  
Primary Aromatic Amines

A one-pot procedure for the synthesis of biologically relevant coumarin-hydrazones by a three-component reaction between 4-hydrocoumarins, primary aromatic amines and tert-butyl nitrite under ball-milling in the absence of any catalyst/additive...

scholarly journals Synthesis of Organic Ligands via Reactions of 4-Benzoyl-5-phenylamino-2,3-dihydrothiophene-2,3-dione with N-Nucleophiles

2020 ◽  
Vol 2020 ◽  
pp. 1-9
Author(s):  
Hassan Kabirifard ◽  
Pardis Hafez Taghva ◽  
Hossein Teimouri ◽  
Niloofar Koosheshi ◽  
Parastoo Javadpour ◽  
...  
Keyword(s):  
High Temperature ◽  
Carbonyl Group ◽  
Aromatic Amines ◽  
Room Temperature ◽  
Organic Ligands ◽  
Carboxyl Group ◽  
Primary Aromatic Amines

The reaction of 4-benzoyl-5-phenylamino-2,3-dihydrothiophene-2,3-dione (1) with aminoheteroaryls, lamotrigine, 1,3-diaminoheteroaryls, dapsone, NH2R (hydroxylamine, DL-1-phenylethylamine, and metformin), and 4,4′-bipyridine in THF/H2O (1 : 1) at room temperature led to 3-N-phenylthiocarbamoyl-2-butenamides 2–5, while that with naphthylamines and 1,3-phenylenediamine in ethanol at high temperature led to 5-phenylamino-2,5-dihydrothiophene-2-ones 6–8 as organic ligands in the medium to good yields. These showed the nucleophilic attacks of N-nucleophiles, except primary aromatic amines, on thioester carboxyl group (C-2) of thiophene-2,3-dione ring 1. However, the nucleophilic attacks of primary aromatic amines on the carbonyl group (C-3) of thiophene-2,3-dione 1 occurred in the form of substituted thiophenes.

Preparation of aromatic amines by copper-catalyzed coupling of boronic acids with aqueous ammonia

2010 ◽  
Vol 88 (9) ◽  
pp. 964-968 ◽  
Author(s):  
Zhaoqiong Jiang ◽  
Zhiqing Wu ◽  
Lixia Wang ◽  
Di Wu ◽  
Xiangge Zhou
Keyword(s):  
Aromatic Amines ◽  
Aqueous Ammonia ◽  
Environmentally Friendly ◽  
Boronic Acids ◽  
Reaction Conditions ◽  
Highly Efficient ◽  
Primary Aromatic Amines

A simple, highly efficient, and environmentally friendly protocol for the synthesis of primary aromatic amines by catalytic coupling of aromatic boronic acids with aqueous ammonia has been developed by using commercial and inexpensive CuSO4·5H2O as catalyst without addition of other solvents under mild reaction conditions.

Sign in / Sign up

Export Citation Format

Share Document