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3-Quinolinecarboxamide, also known as 3-Quinolinecarboxylic acid amide, is a chemical compound characterized by its molecular formula C10H8N2O. It is a white powder that is soluble in organic solvents but not in water. This versatile compound is recognized for its potential applications in medicine and agriculture, primarily due to its ability to inhibit certain enzymes and receptors involved in various diseases.

6480-67-7

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6480-67-7 Usage

Uses

Used in Pharmaceutical Synthesis:
3-Quinolinecarboxamide is used as a building block for the synthesis of various pharmaceuticals and agrochemicals. Its chemical properties make it a valuable component in the development of new drugs and pesticides.
Used in Antimicrobial Applications:
3-Quinolinecarboxamide is used as an antimicrobial agent, leveraging its ability to inhibit the growth of certain microorganisms. This makes it a potential candidate for use in treatments and products aimed at controlling microbial infections.
Used in Antiviral Applications:
3-Quinolinecarboxamide is used as an antiviral agent, exhibiting activity against specific viruses. Its antiviral properties are attributed to its capacity to interfere with viral replication and infection processes.
Used in Cancer Treatment Research:
3-Quinolinecarboxamide is used as a potential therapeutic agent in cancer research. It is being studied for its ability to inhibit enzymes and receptors that play a role in the development and progression of cancer.
Used in Neurodegenerative Disease Research:
3-Quinolinecarboxamide is used in the investigation of treatments for neurodegenerative diseases. Its potential to inhibit certain enzymes and receptors involved in these conditions positions it as a candidate for further research and development in this area.

Check Digit Verification of cas no

The CAS Registry Mumber 6480-67-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,4,8 and 0 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6480-67:
(6*6)+(5*4)+(4*8)+(3*0)+(2*6)+(1*7)=107
107 % 10 = 7
So 6480-67-7 is a valid CAS Registry Number.

6480-67-7Relevant academic research and scientific papers

Preparation of substituted quinolinyl and isoquinolinyl sulfonyl chlorides for the synthesis of novel sulfonamides

Lai, Justine Y. Q.,Ferguson, Yvonne,Jones, Mark

, p. 3427 - 3433 (2003)

Novel sulfonyl chlorides of quinolines and isoquinolines have successfully been prepared. This enabled the preparation of the corresponding sulfonamides via reaction with an amine using the "resin-capture and release" methodology.

Novel quinazoline-quinoline alkaloids with cytotoxic and DNA topoisomerase II inhibitory activities

Ma, Zhongze,Hano, Yoshio,Nomura, Taro,Chen, Yingjie

, p. 1193 - 1196 (2004)

Two new synthetic analogues of luotonins A and F, 7-acetylaminoluotonin A (6) and 3-[3H(quinazolino-4-one)]quinoline (7) were synthesized. The new analogues, along with four natural quinazoline-quinoline alkaloids, luotonins A (1), B (2), E (3), F (4) and a synthetic deoxoluotonin F (5), showed cytotoxic activity (IC50 1.8-40.0 μg/mL) and DNA topoisomerase II inhibition at a concentration of 25 μM.

Direct Oxidative Amination of the Methyl C-H Bond in N-Heterocycles over Metal-Free Mesoporous Carbon

Long, Xiangdong,Wang, Jia,Gao, Guang,Nie, Chao,Sun, Peng,Xi, Yongjie,Li, Fuwei

, p. 10902 - 10912 (2021/09/08)

Direct oxidative amination of the sp3C-H bond is an attractive synthesis route to obtain amides. Conventional catalytic systems for this transformation are based on transition metals and complicated synthesis processes. Herein, direct and efficient oxidative amination of the methyl C-H bond in a wide range of N-heterocycles to access the corresponding amides over metal-free porous carbon is successfully developed. To understand the fundamental structure-activity relationships of carbon catalysts, the surface functional groups and the graphitization degree of porous carbon have been purposefully tailored through doping with nitrogen or phosphorus. The results of characterization, kinetic studies, liquid-phase adsorption experiments, and theoretical calculations indicate that the high activity of the carbon catalyst is attributed to the synergistic effect of surface acidic functional groups (hydroxyl/carboxylic acid/phosphate) and more graphene edge structures exposed on the surface of carbon materials with a high graphitization degree, in which the role of acidic functional groups is to adsorb the substrate molecule and the role of the graphene edge structure is to activate O2

Sodium sulphide promoted synthesis of fused quinoline at room temperature

Singh, Rashmi,Sharma, Vishal Prasad,Yadav, Priyanka,Sonker, Priyanka,Singh, Radhey Mohan,Tewari, Ashish Kumar

supporting information, p. 8108 - 8112 (2021/10/04)

A novel, simple and eco-friendly strategy for the synthesis of thiopyrano[4,3-b]quinolin-1-ones and pyrrolo[3,4-b]quinolin-1-ones from 2-alkynylquinoline-3-carbonitriles and sodium sulphide (Na2S·9H2O) under catalyst-free conditions at room temperature has been described. In this reaction, a readily available inorganic salt (Na2S·9H2O) serves as the sulphur source and leads to the generation of diverse functionalized thiopyrano[4,3-b]quinolin-1-ones and pyrrolo[3,4-b]quinolin-1-ones in moderate to excellent yields through sulfuration, annulation, and aerial oxidation.

Water-soluble superbulky (η6- p -cymene) ruthenium(ii) amine: An active catalyst in the oxidative homocoupling of arylboronic acids and the hydration of organonitriles

Nirmala, Muthukumaran,Adinarayana, Mannem,Ramesh, Karupnaswamy,Maruthupandi, Mannarsamy,Vaddamanu, Moulali,Raju, Gembali,Prabusankar, Ganesan

supporting information, p. 15221 - 15230 (2018/09/29)

A phosphine free water-soluble superbulky amine-ruthenium-arene complex (2) encompassing 2,6-bis(diphenylmethyl)-4-methylaniline was synthesised in good yield. 2 was characterized by FT-IR, 1H NMR, and 13C NMR spectroscopies, TGA and elemental analyses. The structure of 2 was confirmed by a single-crystal X-ray diffraction study. The ruthenium centre in 2 adopts the pseudo-octahedral geometry due to the η6-p-cymene ring and bulky aniline ligand along with two chloro groups. Besides, complex 2 was efficaciously employed as a catalyst in the hydration of organonitriles to amides. This reaction proceeds efficiently for a wide range of substrates in an environmentally benign medium and is an economically reasonable synthetic route to amides in good yields. In addition, 2 acts as an excellent catalyst in the oxidative homocoupling of arylboronic acids in water. A range of arylboronic acids undergo a homocoupling reaction in the presence of catalyst 2 to yield symmetrical biaryls in reasonable to good yields.

Ruthenium(II) complexes incorporating salicylaldiminato-functionalized N-heterocyclic carbene ligands as efficient and versatile catalysts for hydration of organonitriles

Nirmala, Muthukumaran,Saranya, Gandhi,Viswanathamurthi, Periasamy

, p. 134 - 144 (2016/01/09)

We describe a new synthetic procedure for synthesis of ruthenium(II) complexes containing salicylaldiminato functionalized mixed N-heterocyclic carbene (NHC) ligand and phosphine co-ligand. The complexes (3a-3d) have been obtained in good to excellent yields by transmetalation from the corresponding Ag-NHC complexes (2a-2d) as carbene transfer reagents. All the [Ru-NHC] complexes have been characterized by elemental analyses, spectroscopic methods as well as ESI mass spectrometry. The ligands 1a-1d show their versatility by switching to be O,N,C-chelating in these ruthenium(II) complexes. The resulting complexes have been evaluated as potential catalysts for the selective hydration of nitriles to primary amides, and related amide bond forming reactions, in environmentally friendly medium. The reaction tolerated ether, hydroxyl, nitro, bromo, formyl, pyridyl, benzyl and alkyl functional groups. The catalyst was stable for weeks and could be recovered and reused more than six times without significant loss of activity.

Palladium-catalyzed synthesis of primary benzamides from aryl bromides via a cyanation and hydration sequence

Sharif, Muhammad,Wu, Xiao-Feng

, p. 21001 - 21004 (2015/03/30)

An interesting and effective procedure for the synthesis of benzamides from aryl bromides has been developed. In the presence of a palladium catalyst, various primary benzamides have been produced in moderate to excellent yields in a one-pot one-step manner.

Pd(0)-mediated [11C]carbonylation of aryl and heteroaryl boronic acid pinacol esters with [11C]carbon monoxide under ambient conditions and a facile process for the conversion of [carbonyl-11C]esters to [carbonyl-11C]amides

Ishii, Hideki,Minegishi, Katsuyuki,Nagatsu, Koutaro,Zhang, Ming-Rong

supporting information, p. 1588 - 1596 (2015/03/04)

A new method has been developed for the Pd(0)-mediated [11C]carbonylation of aryl/heteroaryl boronic acid pinacol esters with [11C]carbon monoxide in the presence of p-benzoquinone and triphenylphosphine in a mixture of N,N-dimethylformamide (DMF) and methanol (MeOH) or just MeOH under ambient pressure at 65 °C. This method was used to convert a variety of different aryl/heteroaryl boronates to the corresponding [carbonyl-11C]esters with decay-corrected radiochemical yields in the range of 6-80%. Furthermore, some of these [carbonyl-11C]esters were treated with sodium hydroxide or aqueous ammonium to give the corresponding [carbonyl-11C]carboxylic acids and amides, respectively. This new method was also used to achieve the direct syntheses of [11C]aspirin using water or tetramethylammonium hydroxide as the nucleophile instead of MeOH in DMF.

Substrate-Specific Heterogeneous Catalysis of CeO2 by Entropic Effects via Multiple Interactions

Tamura, Masazumi,Sawabe, Kyoichi,Tomishige, Keiichi,Satsuma, Atsushi,Shimizu, Ken-Ichi

, p. 20 - 26 (2015/04/27)

Achieving complete substrate specificity through multiple interactions like an enzyme is one of the ultimate goals in catalytic studies. Herein, we demonstrate that multiple interactions between the CeO2 surface and substrates are the origin of substrate-specific hydration of nitriles in water by CeO2, which is exclusively applicable to the nitriles with a heteroatom (N or O) adjacent to the α-carbon of the CN group but is not applicable to the other nitriles. Kinetic studies reveal that CeO2 reduces the entropic barrier (TΔS?) for the reaction of the former reactive substrate, leading to 107-fold rate enhancement compared with the latter substrate. Density functional theory (DFT) calculations confirmed multiple interaction of the reactive substrate with CeO2, as well as preferable approximation and alignment of the nitrile group of the substrate to the active OH group on CeO2 surface. This can lead to the reduction of the entropic barrier. This is the first example of an entropy-driven substrate-specific catalysis of a nonporous metal oxide surface, which will provide a new design strategy for enzyme-inspired synthetic catalysts.

Mild and selective heterogeneous catalytic hydration of nitriles to amides by flowing through manganese dioxide

Battilocchio, Claudio,Hawkins, Joel M.,Ley, Steven V.

supporting information, p. 1060 - 1063 (2016/10/17)

A sustainable flow chemistry process for the hydration of nitriles, whereby an aqueous solution of the nitrile is passed through a column containing commercially available amorphous manganese dioxide, has been developed. The product is obtained simply by concentration of the output stream without any other workup steps. The protocol described is rapid, robust, reliable, and scalable, and it has been applied to a broad range of substrates, showing a high level of chemical tolerance.

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