Academic literature on the topic '2-aminobenzonitrile'

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Journal articles on the topic "2-aminobenzonitrile"

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Ru, Zong-Ling, and Guo-Xi Wang. "Bis(2-aminobenzonitrile)tetraaquacobalt(II) dichloride." Acta Crystallographica Section E Structure Reports Online 65, no. 12 (2009): m1688. http://dx.doi.org/10.1107/s1600536809050272.

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Marinho, Elina, and M. Proença. "The Reaction of 2-(Acylamino)benzonitriles with Primary Aromatic Amines: A Convenient Synthesis of 2-Substituted 4-(Arylamino)quinazolines." Synthesis 47, no. 11 (2015): 1623–32. http://dx.doi.org/10.1055/s-0034-1380322.

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2-Substituted 4-(arylamino)quinazolines were prepared from 2-(acylamino)benzonitriles and primary arylamines by refluxing in either ethanol using trifluoroacetic acid as a catalyst or acetic acid. The 2-aminobenzonitrile was acylated by reaction with anhydrides, isocyanates, or ethyl chloroformate at room temperature.
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Sheng, Zhi-Zheng, Min-Min Huang, Teng Xue, Fei Xia, and Hai-Hong Wu. "Alcohol amine-catalyzed CO2 conversion for the synthesis of quinazoline-2,4-(1H,3H)-dione in water." RSC Advances 10, no. 57 (2020): 34910–15. http://dx.doi.org/10.1039/d0ra06439d.

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Commercial DEA is proposed for efficiently promoting the cyclization of CO<sub>2</sub> and 2-aminobenzonitrile to quinazoline-2,4(1H,3H)-dione (up to 94% yield) while water acts as the solvent and co-catalyst.
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Fuster, Marta G., Imane Moulefera, Mercedes G. Montalbán, José Pérez, Gloria Víllora, and Gabriel García. "Synthesis and Characterization of New Ruthenium (II) Complexes of Stoichiometry [Ru(p-Cymene)Cl2L] and Their Cytotoxicity against HeLa-Type Cancer Cells." Molecules 27, no. 21 (2022): 7264. http://dx.doi.org/10.3390/molecules27217264.

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When the [Ru(p-cymene)(μ-Cl)Cl]2 complex is made to react, in dichloromethane, with the following ligands: 2-aminobenzonitrile (2abn), 4-aminobenzonitrile (4abn), 2-aminopyridine (2ampy) and 4-aminopyridine (4ampy), after addition of hexane, the following compounds are obtained: [Ru(p-cymene)Cl2(2abn)] (I), [Ru(p-cymene)Cl2(4abn)] (II), [Ru(p-cymene)Cl2(2ampy] (III) and [Ru(p-cymene)Cl2(μ-(4ampy)] (IV). All the compounds are characterized by elemental analysis of carbon, hydrogen and nitrogen, proton nuclear magnetic resonance, COSY 1H-1H, high-resolution mass spectrometry (ESI), thermogravime
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Boukthir, Mona, Fathi Zribi, Mohamed Belhouchet, and Fakher Chabchoub. "A Facile Synthesis of Pyrimidoquinazoline Derivatives." JOURNAL OF ADVANCES IN CHEMISTRY 7, no. 3 (2011): 1434–39. http://dx.doi.org/10.24297/jac.v7i3.2379.

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A series of pyrimidoquinazoline are prepared via the reaction of ethyl 2,2-dicyano-1-arylvinylcarbamate derivatives 1a-b with methyl 2-aminobenzoate, 1-(2-aminophenyl)ethanone and 2-aminobenzonitrile. The reactivity of compounds 1a-b toward 3-amino-4,6-diphénylnicotinonitrile are studied. The structures of the synthesized compounds are elucidated by X-ray diffraction, IR spectroscopy and nuclear magnetic resonance.
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Ahuja, I. S., and Shailendra Tripathi. "X-ray diffraction studies on dichloro-(2-aminobenzonitrile)copper(II)." Crystal Research and Technology 25, no. 6 (1990): K130—K132. http://dx.doi.org/10.1002/crat.2170250623.

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Lang, Xian-Dong, Shuai Zhang, Qing-Wen Song, and Liang-Nian He. "Tetra-butylphosphonium arginine-based ionic liquid-promoted cyclization of 2-aminobenzonitrile with carbon dioxide." RSC Advances 5, no. 20 (2015): 15668–73. http://dx.doi.org/10.1039/c4ra16057f.

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Tetra-butylphosphonium arginine-based IL able to activate both amino-groups and CO<sub>2</sub> proved to be an efficient and recyclable catalyst for the synthesis of quinazoline-2,4(1H,3H)-diones from 2-aminobenzonitriles and CO<sub>2</sub> under solvent-free conditions.
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Brodersen, Klaus, and Jürgen Hofmann. "Synthese und Kristallstruktur von Bis(o-aminobenzonitril)-diquecksilber(I)-dinitrat / Synthesis and Crystal Structure of Bis(o-aminobenzonitrile)dimercury(I)-dinitrate." Zeitschrift für Naturforschung B 46, no. 12 (1991): 1684–88. http://dx.doi.org/10.1515/znb-1991-1217.

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[Hg2(o-NH2C6H4CN)2](NO3)2 is formed by the reaction of o-aminobenzonitrile with dimercury(I)-dinitrate in methanol. It crystallizes in the monoclinic space group P 2/c with a = 8.6819(5)Å, b = 5.3696(6)Å, c = 19.7645(8)Å, β = 95.138(12)° and Ζ = 2. The crystal structure has been determined by single crystal X-ray diffraction with applied gaussian absorption correction and refined to an Rw-value of 0.027.The Hg22+-ion is coordinated to both amino nitrogen atoms. Strong hydrogen bonds and bridging nitrate ions lead to chain structure.
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Jonathan Fray, M., Paul Allen, Paul R. Bradley, et al. "Synthesis of 5-Heterocyclic Substituted Quinazolin-4-ones via 2-Aminobenzonitrile Derivatives." HETEROCYCLES 67, no. 2 (2006): 489. http://dx.doi.org/10.3987/com-05-s(t)17.

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Moitsheki, Lesego J., Susan A. Bourne та Luigi R. Nassimbeni. "catena-Poly[[bis(thiocyanato-κN)cobalt(II)]-di-μ-2-aminobenzonitrile-κ2N,N′]". Acta Crystallographica Section E Structure Reports Online 61, № 12 (2005): m2580—m2581. http://dx.doi.org/10.1107/s1600536805036846.

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Dissertations / Theses on the topic "2-aminobenzonitrile"

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El, Haj Brahim Ichrak. "Préparation stéréosélective de 2-alcynyldiols-1,3 ou 2-alcynylaminoalcools-1,3 : synthèse des hétérocycles condensés issus du 2- aminobenzonitrile." Electronic Thesis or Diss., Sorbonne université, 2023. https://accesdistant.sorbonne-universite.fr/login?url=https://theses-intra.sorbonne-universite.fr/2023SORUS495.pdf.

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Cette thèse s'est orientée autour de deux axes de recherche distincts. En premier lieu, nous avons exploré la synthèse des 4-hydroxy-1-boryl-1-allenylsilanes, en adoptant une approche innovante à partir d'époxydes acétyléniques et du (triéthylsilyl)pinacolborane. Cette méthode a permis une préparation stéréosélective et stéréospécifique d'allénylboranes, suivant un mécanisme SNi anti. De plus, l'utilisation de ces 4-hydroxy-1-boryl-1-allenylsilanes pour la propargylation des aldéhydes a conduit, de manière stéréosélective, aux 2-alcynyldiols-1,3. Un état de transition impliquant une structure
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Book chapters on the topic "2-aminobenzonitrile"

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Döpp, H., and D. Döpp. "Diazotization of 2-Aminobenzonitrile or Aminohetarenecarbonitrile/Cyclization with Primary Amines." In Six-Membered Hetarenes with Two Unlike or More than Two Heteroatoms and Fully Unsaturated Larger-Ring Heterocycles. Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-017-00424.

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Larsen, R. D. "From Anthranilates or 2-Aminobenzonitriles." In Six-Membered Hetarenes with One Nitrogen or Phosphorus Atom. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-015-00930.

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Kikelj, D. "From 2-Aminobenzonitriles and Nitriles." In Six-Membered Hetarenes with Two Identical Heteroatoms. Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-016-00766.

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Kikelj, D. "From 2-Aminobenzonitriles and Formic Acid." In Six-Membered Hetarenes with Two Identical Heteroatoms. Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-016-00790.

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Kikelj, D. "From 2-Aminobenzonitriles and Guanidines, Imidates, or Formimidamides." In Six-Membered Hetarenes with Two Identical Heteroatoms. Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-016-00765.

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Kikelj, D. "From 2-Aminobenzonitriles and Formamide or 1,3,5-Triazine." In Six-Membered Hetarenes with Two Identical Heteroatoms. Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-016-00767.

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Kikelj, D. "From 2-Aminobenzonitriles and Thioamides or Thioacetic Acid." In Six-Membered Hetarenes with Two Identical Heteroatoms. Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-016-00791.

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Kikelj, D. "From 2-Aminobenzonitriles and Chlorosulfonyl Isocyanate, Urea, or Thiourea." In Six-Membered Hetarenes with Two Identical Heteroatoms. Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-016-00764.

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Döpp, H., and D. Döpp. "Cyclization of 2-Aminobenzonitriles and Related Compounds with Nitric Acid." In Six-Membered Hetarenes with Two Unlike or More than Two Heteroatoms and Fully Unsaturated Larger-Ring Heterocycles. Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-017-00417.

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Kikelj, D. "From 2-Aminobenzonitriles, Grignard Reagents, and Carbonyl Compounds or Phosgene Iminium Chlorides." In Six-Membered Hetarenes with Two Identical Heteroatoms. Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-016-00792.

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Conference papers on the topic "2-aminobenzonitrile"

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Molis, Steven E., and Robert J. Twieg. "Fourier-transform IR characterization of molecular orientation in poled polymer glasses." In OSA Annual Meeting. Optica Publishing Group, 1990. http://dx.doi.org/10.1364/oam.1990.the2.

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The electro-optical activity of organic, nonlinear optical (NLO) systems in part depends on the extent of molecular orientation of the NLO moiety. In this investigation, the technique of using infrared absorption spectroscopy to characterize molecular orientation is introduced as a means of characterizing orientational order in poled polymer glasses. A quantitative understanding of this orientation can be used in modeling the field-induced orientation of a dipole as well as for determining the polarizabilities of new NLO substituents. In this initial investigation the orientation of organic gu
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