Month: November 2022

On September 1, 2018, Nikseresht, Ahmad; Ghasemi, Saba; Parak, Soraya published an article.Safety of 2-Aminomalononitrile 4-methylbenzenesulfonate The title of the article was [Cu3(BTC)2]: A metal-organic framework as an environment-friendly and economically catalyst for the synthesis of tacrine analogues by Friedlaender reaction under conventional and ultrasound irradiation. And the article contained the following:

Using a green and simple route with ultrasound illumination, atm. pressure and room temperature, for synthesizing tacrine analogs in the presence of [Cu3(BTC)2] as an environment-friendly and economically catalyst was considered. [Cu3(BTC)2] is one of the heterogeneous catalysts on hand capable of being employed, in the Friedlaender reaction, whenever 5-amino-4-cyano-2-phenyl-1,3-oxazole and appropriately substituted carbonyl derivatives under conventional and ultrasonic irradiation The results of this study indicate that the active sites in the [Cu3(BTC)2] for synthesis of cyclohepta[b]oxazolo[4,5-e]pyridine are mainly copper atoms and the role of Bronsted acid organic ligand in the MOF is negligible. These procedures were properly arranged to provide the utmost yields in a short while. The crystal stability in the process of catalysis was studied by various techniques such as XRD, BET and ICP that demonstrate excellent stability in reaction conditions. The experimental process involved the reaction of 2-Aminomalononitrile 4-methylbenzenesulfonate(cas: 5098-14-6).Safety of 2-Aminomalononitrile 4-methylbenzenesulfonate

The Article related to tacrine analog green preparation friedlaender copper benzenetricarboxylate mof catalyst, Heterocyclic Compounds (More Than One Hetero Atom): Oxazoles, Isoxazoles and other aspects.Safety of 2-Aminomalononitrile 4-methylbenzenesulfonate

Referemce:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts

Freeman, Fillmore; Kim, Darrick S. H. L. published an article in 1989, the title of the article was Preparation of 2-alkyl- and 2-aryl-5-amino-4-cyano-1,3-oxazoles.Application In Synthesis of 2-Aminomalononitrile 4-methylbenzenesulfonate And the article contains the following content:

Aminopropanedinitrile p-toluenesulfonate reacts with acid chlorides to give 5-amino-4-cyano-1,3-oxazoles I (R = Me, Et, CHMe2, Ph, 4-MeOC6H4, 4-O2NC6H4, 2-furyl) in 51-95% yields. The experimental process involved the reaction of 2-Aminomalononitrile 4-methylbenzenesulfonate(cas: 5098-14-6).Application In Synthesis of 2-Aminomalononitrile 4-methylbenzenesulfonate

The Article related to acid chloride cyclocondensation aminomalonitrile tosylate, oxazole amino cyano aryl alkyl, Heterocyclic Compounds (More Than One Hetero Atom): Oxazoles, Isoxazoles and other aspects.Application In Synthesis of 2-Aminomalononitrile 4-methylbenzenesulfonate

Referemce:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts

On June 19, 2009, O’Shea, Paul D.; Gauvreau, Danny; Gosselin, Francis; Hughes, Greg; Nadeau, Christian; Roy, Amelie; Shultz, C. Scott published an article.COA of Formula: C6H3BrN2O The title of the article was Practical Synthesis of a Potent Bradykinin B1 Antagonist via Enantioselective Hydrogenation of a Pyridyl N-Acyl Enamide. And the article contained the following:

A practical and efficient synthesis of bradykinin B1 antagonist I is described. A convergent strategy was utilized which involved synthesis of three fragments: II, III and IV. Cross coupling of fragments II and III followed by amidation with IV enabled efficient synthesis of I in 19 steps total, a 35% overall yield from com. available 5-bromo-3-nitropyridin-2-ol. The key to the success of the synthesis was the development of a fluorodenitration step to install the fluorine in pyridine III and a catalytic enantioselective hydrogenation of N-acyl enamide V to set the stereochem. The experimental process involved the reaction of 5-Bromo-3-hydroxypicolinonitrile(cas: 1160936-51-5).COA of Formula: C6H3BrN2O

The Article related to fluorodenitration rhodium catalyst stereoselective hydrogenation acyl enamide, bradykinin b 1 antagonist stereoselective preparation, Heterocyclic Compounds (More Than One Hetero Atom): Oxazoles, Isoxazoles and other aspects.COA of Formula: C6H3BrN2O

Referemce:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts

On June 15, 2006, Feenstra, Roelof W.; Stoit, Axel; Terpstra, Jan-Willem; Pras-Raves, Maria L.; McCreary, Andrew C.; Van Vliet, Bernard J.; Hesselink, Mayke B.; Kruse, Cornelis G.; Van Scharrenburg, Gustaaf J. M. published a patent.Safety of 3-Chloro-4-nitrobenzonitrile The title of the patent was Preparation of aminoethoxybenzoxazole derivatives with a combination of partial dopamine-d2 receptor agonism and serotonin reuptake inhibition. And the patent contained the following:

Title compounds I [X = S or O; R1 = H, alkyl, CF3, OH , etc.; R2 = H, alkyl, halo, or CN; R3 = H or alkyl; R4 = H, alkyl or haloalkyl; T = (un)saturated, (un)substituted carbon chain wherein one carbon atom may optionally be replaced with a N atom; Ar = aryl or heteroaryl], and their pharmaceutically acceptable salts, are prepared and disclosed to possess capability of both serotonin reuptake inhibition and partial agonism on dopamine -D2 receptors. Thus, e.g., II was prepared by reaction of 2-(4-iodobutoxy)benzonitrile with the corresponding amine (preparation given). I are evaluated by dopamine-D2 and 5-HT reuptake binding assays, e.g., II demonstrate pKi values of 7.9 and 7.4 resp. The invention also relates to the use of a compound disclosed herein for the manufacture of a medicament giving a beneficial effect. The experimental process involved the reaction of 3-Chloro-4-nitrobenzonitrile(cas: 34662-29-8).Safety of 3-Chloro-4-nitrobenzonitrile

The Article related to aminoethoxy benzoxazole preparation dopamine d2 receptor serotonin reuptake inhibitor, cns agent aminoethoxybenzoxazole amine preparation, Heterocyclic Compounds (More Than One Hetero Atom): Oxazoles, Isoxazoles and other aspects.Safety of 3-Chloro-4-nitrobenzonitrile

Referemce:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts

On August 31, 1997, Freeman, Fillmore; Chen, Tao; Van der Linden, Johannes B. published an article.Computed Properties of 5098-14-6 The title of the article was Synthesis of highly functionalized 1,3-oxazoles. And the article contained the following:

A convenient 1-pot method for the preparation of 2-substituted 5-amino-4-cyano-1,3-oxazoles from carboxylic acids and aminomalononitrile tosylate is reported. The experimental process involved the reaction of 2-Aminomalononitrile 4-methylbenzenesulfonate(cas: 5098-14-6).Computed Properties of 5098-14-6

The Article related to cyanooxazolamine preparation, aminooxazolenitrile preparation, oxazole amino cyano preparation, carboxylic acid aminomalononitrile tosylate cyclocondensation, Heterocyclic Compounds (More Than One Hetero Atom): Oxazoles, Isoxazoles and other aspects.Computed Properties of 5098-14-6

Referemce:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts

On March 28, 2012, Spencer, John; Patel, Hiren; Amin, Jahangir; Callear, Samantha K.; Coles, Simon J.; Deadman, John J.; Furman, Christophe; Mansouri, Roxane; Chavatte, Philippe; Millet, Regis published an article.Category: nitriles-buliding-blocks The title of the article was Microwave-mediated synthesis and manipulation of a 2-substituted-5-aminooxazole-4-carbonitrile library. And the article contained the following:

A 2-substituted 5-aminooxazole-4-carbonitrile library has been synthesized and modified via microwave-mediated and flow chemistries. One synthesized compound, 5-(1H-pyrrol-1-yl)-4-(1H-tetrazol-5-yl)-2-(thien-2-yl)oxazole, contains three distinct heterocycles attached to the central oxazole core, highlighting the structural diversity of this approach. Three oxazoles had micromolar ki values against cannabinoid (CB1/CB2) receptors. The experimental process involved the reaction of 2-Aminomalononitrile 4-methylbenzenesulfonate(cas: 5098-14-6).Category: nitriles-buliding-blocks

The Article related to aminooxazolecarbonitrile library preparation reaction, oxazolecarbonitrile amino library preparation reaction, cannabinoid receptor affinity aminooxazolecarbonitrile, Heterocyclic Compounds (More Than One Hetero Atom): Oxazoles, Isoxazoles and other aspects.Category: nitriles-buliding-blocks

Referemce:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts

On February 7, 2008, Aleman, Jose; Jacobsen, Christian Borch; Frisch, Kim; Overgaard, Jacob; Jorgensen, Karl Anker published an article.Application of 2510-01-2 The title of the article was Organocatalytic asymmetric vinylogous addition to quinones – formation of optically active α-aryl ketones. And the article contained the following:

The organocatalytic addition of dicyanoalkylidenes to quinones catalyzed by cinchona alkaloids to give 1,4-diketones with high diastereomeric ratios (up to >98:<2 dr) and enantioselectivities (up to 99% ee) has been developed; the optically active compounds obtained are useful for a number of transformations, e.g. the synthesis of optically active α-aryl ketones. The experimental process involved the reaction of 2-(2,3-Dihydro-1H-inden-1-ylidene)malononitrile(cas: 2510-01-2).Application of 2510-01-2

The Article related to quinone stereoselective addition alkylidenemalononitrile cinchona alkaloid catalyst, ketone aromatic asym synthesis, Benzene, Its Derivatives, and Condensed Benzenoid Compounds: Naphthalenes and other aspects.Application of 2510-01-2

Referemce:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts

Grivsky, Eugene M.; Hitchings, George H. published an article in 1974, the title of the article was Syntheses of 2-chloro-4-acetylaminobenzonitrile isomers and structurally related compounds with biological activities.Quality Control of 3-Chloro-4-nitrobenzonitrile And the article contains the following content:

Benzonitriles I, II, and III (Xn = 2-,3-Cl, 2-F, 2,6-, 2,4 -Cl2; NH2, NHCOR, NO2 in 2, 4, or 5 position; R = e.g., Me, H, CF3, CHCl2, CH2Cl, Et, Me2CH, Pr, CH:CHCO2H, CH2CH2CO2H) were prepared (5 I, 15 II and 88 III). E.g., reaction of 2,4-F-(O2N)C6H3CO2H with MeSO2NH2-PCl5 gave 96% I (Xn = 2-F, 4-NO2), which was reduced to give II (Xn = 2-F, 4-NH2), which was acetylated to give 95% III (Xn = 2-F, R = Me). III (Xn = 2-Cl, NHCOMe in 4 position) had LD50 (oral-mice)of 1800 mg/kg; and at 20 mg/kg (oral-mice) was an antide-pressant and at 25 and 50 mg kg (orally-rat), resp., was an anal-gesic and antipyretic. The experimental process involved the reaction of 3-Chloro-4-nitrobenzonitrile(cas: 34662-29-8).Quality Control of 3-Chloro-4-nitrobenzonitrile

The Article related to acetanalide cyano halo analgesic, antipyretic chloroacetamidobenzonitrile, antidepressant chloroacetamidobenzonitrile, Noncondensed Aromatic Compounds: Nitriles, Isonitriles, and Acyl Cyanides and other aspects.Quality Control of 3-Chloro-4-nitrobenzonitrile

Referemce:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts

On September 30, 1989, Freeman, Fillmore; Kim, Darrick S. H. L. published an article.Recommanded Product: 5098-14-6 The title of the article was Preparation of (E,E)-4-amino-1-aryl-3-cyano-4-methoxy-2-azabutadienes. And the article contained the following:

Treatment of (NC)2CHN+H3 4-MeC6H4SO3- with NaOAc and RCHO (R = Ph, 2-BrC6H4, 2-ClC6H4, 2-O2NC6H4, 4-O2NC6H4, 4-HOC6H4, 2-naphthyl) in MeOH gave 23-99% (E,E)-RCH:NC(CN):C(OMe)NH2. The experimental process involved the reaction of 2-Aminomalononitrile 4-methylbenzenesulfonate(cas: 5098-14-6).Recommanded Product: 5098-14-6

The Article related to ammoniomalononitrile tosylate condensation aromatic aldehyde, aminoarylcyanomethoxyazabutadiene, azabutadiene aminoarylcyanomethoxy, Benzene, Its Derivatives, and Condensed Benzenoid Compounds: Naphthalenes and other aspects.Recommanded Product: 5098-14-6

Referemce:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts

Taylor, Edward C.; Jacobi, Peter A. published an article in 1973, the title of the article was Pteridines. XXX. Facile synthesis of xanthopterin.Reference of 2-Aminomalononitrile 4-methylbenzenesulfonate And the article contains the following content:

Pterin 8-oxide (I) rearranges quant. to xanthopterin (II) upon dissolution in a mixture of CF3CO2H/(CF3CO)2O at 50°. The experimental process involved the reaction of 2-Aminomalononitrile 4-methylbenzenesulfonate(cas: 5098-14-6).Reference of 2-Aminomalononitrile 4-methylbenzenesulfonate

The Article related to pterin oxide rearrangement xanthopterin, Heterocyclic Compounds (More Than One Hetero Atom): Purines and Pteridines and other aspects.Reference of 2-Aminomalononitrile 4-methylbenzenesulfonate

Referemce:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts