Category: 100-70-9

Duan, Xiyan published the artcileOne-Pot Synthesis of N-Substituted Enaminones from Ketones, Aromatic Nitriles and Halides, SDS of cas: 100-70-9, the main research area is nitrogen substituted enaminone diastereoselective preparation; ketone nitrile aryl halide copper catalyst tandem Ullmann aldol.

A simple and convenient one-pot copper-catalyzed synthesis of N-substituted enaminones I [R1 = n-Pr, 4-MeC6H4, 2-naphthyl, etc.; R2 = Me, Ph, 4-FC6H4, etc.; Ar = Ph, 2-pyridyl, 4-ClC6H4, 4-BrC6H4, 4-MeC6H4] was demonstrated from ketones, aromatic nitriles and halides. This transformation involved the aldol-type reaction and Ullmann-type cross coupling, which featured high efficient and inexpensive Cu-catalyst with broader diversification scope.

ChemistrySelect published new progress about Aldol addition catalysts, stereoselective. 100-70-9 belongs to class nitriles-buliding-blocks, name is Picolinonitrile, and the molecular formula is C6H4N2, SDS of cas: 100-70-9.

Referemce:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts

Muley, Arabinda published the artcileSynthesis, structure, spectral, redox properties and anti-cancer activity of Ruthenium(II) Arene complexes with substituted Triazole Ligands, Computed Properties of 100-70-9, the main research area is cymene ruthenium pyridyltriazolylpyridine preparation crystal mol structure antitumor activity; arene ruthenium pyridyltriazolylpyridine complex preparation crystal mol structure antitumor.

Three versatile half-sandwich ruthenium(II) p-cymene complexes bearing substituted triazole ligands exhibit promising cancer cell growth inhibition activity towards A549 lung adenocarcinoma and MDA-MB-231 breast adenocarcinoma cells. In this context, the triazole based phthalimide protected new ligand (2-(3, 5-di(pyridin-2-yl)-4H-1,2,4-triazol-4-yl)isoindoline-1,3-dione) (L1) was prepared Three ruthenium(II) p-cymene complexes [Ru(η6-p-cymene)(L1)Cl]Cl: [1]Cl, L1: (2-(3,5-di(pyridin-2-yl)-4H-1,2,4-triazol-4-yl)isoindoline-1,3-dione), [Ru(η6-p-cymene)(L2)Cl]Cl: [2]Cl and [Ru(η6-p-cymene)(L2)Cl](PF6): [2](PF6), L2 (2,2′-(4-(1H-pyrrol-1-yl)-4H-1,2,4-triazole-3,5-diyl)dipyridine) have been successfully synthesized and characterized by different spectral and anal. tools. Pyrrole protected substituted ruthenium complexes [2]Cl and [2](PF6) have been successfully identified structurally by single-crystal x-ray diffraction studies and confirmed the successful anion exchange. The redox properties of the ligands and the targeted metal complexes have been carefully examined Cellular staining, live-cell imaging and MTT assay have been performed for all the complexes. Authors have demonstrated that their synthesized ruthenium(II) p-cymene complexes are capable of inducing significant cytotoxicity in A549 lung cancer cell lines, with an IC50 values of 6.56 ± 0.31μM, 4.74 ± 0.2μM and 13.67 ± 0.64μM and in MDA-MB-231 breast cancer cell lines with an IC50 values of 1.13 ± 0.046μM, 0.36 ± 0.016μM and 11.32 ± 0.49μM for [1]Cl, [2]Cl and [2](PF6) resp.

Journal of Organometallic Chemistry published new progress about Antitumor agents (mammary gland and lung). 100-70-9 belongs to class nitriles-buliding-blocks, name is Picolinonitrile, and the molecular formula is C6H4N2, Computed Properties of 100-70-9.

Referemce:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts

Snead, David R. published the artcileAn improved Balz-Schiemann reaction enabled by ionic liquids and continuous processing, Application of Picolinonitrile, the main research area is verubecestat synthetic intermediate synthesis; Balz Schiemann cyanopyridinamine ionic liquid continuous process safety; cyanofluoropyridine synthesis.

A Balz-Schiemann reaction was developed to convert 2-cyano-5-aminopyridine to 2-cyano-5-fluoropyridine. The use of an ionic liquid (1-butyl-3-methylimidazolium tetrafluoroborate, BMIMBF4) as a solvent was found to be critical in achieving high assay yields and high selectivity for the fluorination vs. protonation. A process was developed to recycle and reuse the ionic liquid enabling its cost-effective use as a solvent. Finally, the optimal conditions were demonstrated under as a continuous process to address process safety risks associated with diazonium intermediates and the product was used to access a key intermediate in the synthesis of β-amyloid cleaving enzyme 1 inhibitor, verubecestat.

Tetrahedron published new progress about Flow reactors (for continuous processing). 100-70-9 belongs to class nitriles-buliding-blocks, name is Picolinonitrile, and the molecular formula is C6H4N2, Application of Picolinonitrile.

Referemce:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts

Kannaka, Kento published the artcileSynthesis of an amphiphilic tetrazine derivative and its application as a liposomal component to accelerate release of encapsulated drugs, Name: Picolinonitrile, the main research area is amphiphilic tetrazine derivative liposomal; Amphiphilic material; Bioorthogonal chemistry; Controlled release; Drug delivery system; Liposome; Tetrazine.

Tetrazine irreversibly reacts with dienophiles, and its derivatives find wide applications in the fields of biochem. and biophysics. We have synthesized an amphiphilic tetrazine derivative (2-hexadecyl-N-(6-(6-(pyridin-2-yl)-1,2,4,5-tetrazine-3-yl)pyridin-3-yl)octadecanamide; 1), which has a hydrophilic tetrazine structure and hydrophobic alkyl chains. Liposomes composed of compound 1 and 1-palmitoyl-2-oleoylphosphatidylcholine (POPC) (PTz-liposome) were prepared In search of a new drug delivery system (DDS), we investigated the viability of inverse electron-demand Diels-Alder, a reaction between tetrazine and 2-norbornene, on the surface of the liposomes to change membrane fluidity and promote spatial and temporal controlled release of the encapsulated drugs. Compound 1 was synthesized with a yield of 71%. MS anal. after incubation of 2-norbornene with PTz-liposome revealed the binding of 2-norbornene to tetrazine. Indium-111-labeled diethylenetriaminepentaacetic acid (111In-DTPA) was encapsulated inside PTz-liposome to evaluate the leakage of free 111In-DTPA from the liposomes quant. After 24 h of adding 2-norbornene, the release percentage for PTz-liposome was significantly higher than that for the control liposome (without tetrazine structure). Furthermore, the membrane fluidity of the PTz-liposome was increased by adding 2-norbornene. These results suggested that the combination of dienophile and liposome containing a newly synthesized tetrazine derivative can be used as a controlled release DDS carrier.

Bioorganic & Medicinal Chemistry published new progress about Controlled-release drug delivery systems. 100-70-9 belongs to class nitriles-buliding-blocks, name is Picolinonitrile, and the molecular formula is C6H4N2, Name: Picolinonitrile.

Referemce:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts

Liu, Ch. published the artcileSynthesis and Properties of Main-Chain Phosphorescent Polymer with Iridium Complex, Category: nitriles-buliding-blocks, the main research area is mainchain phosphorescent polymer iridium complex.

The main-chain phosphorescent polymers, PFCzIr(PhStz) and PFOIr(PhStz) with iridium complex (4-BrPhBt)2Ir(Pytz), are synthesized by the Suzuki polycondensation, in which the fluorene-carbazole and fluorene segments are used as a polymer backbone. The studied photoluminescent and electroluminescent properties demonstrate good overlap of the emission spectra of poly(fluorene-carbazole) (PFCz) or polyfluorene (PFO) host and the absorption spectra of the iridium complex guest that meets requirements for the efficient Forster transfer from the host polymer to the iridium complex in polymers. With the increase of the content of iridium complex, the host emission intensity decreases, while the guest emission intensity gradually increases. As compared with PFOIr(PhStz), host-guest system in PFCzIr(PhStz) is more efficient in Forster energy transfer, and the photoluminescence and electroluminescence properties are more sound. Among all polymers, PFCzIr(PhStz) 5.0 demonstrates the best performance in electroluminescence, its fluorescence quantum is 22.74%. The devices fabricated from PFCzIr(PhStz)5.0 exhibit yellow-red emission with a maximum brightness of 1568 cd/m2 at 14 V, luminous efficiency and power efficiency reach 6.24 cd/A and 2.45 lm/w.

Russian Journal of General Chemistry published new progress about Electric current-potential relationship. 100-70-9 belongs to class nitriles-buliding-blocks, name is Picolinonitrile, and the molecular formula is C6H4N2, Category: nitriles-buliding-blocks.

Referemce:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts

Wrzeszcz, Zuzanna published the artcileHeteroaromatic N-oxides modified with a chiral oxazoline moiety, synthesis and catalytic applications, SDS of cas: 100-70-9, the main research area is oxazoline chiral heteroaromatic nitrogen oxide preparation stereoselective catalytic reaction; heteroaromatic oxide preparation oxidation amino alc heterocyclization.

A multi-step synthesis of a series of chiral oxazoline substituted pyridine N-oxides I (R1 = i-pr, t-bu, Ph; R2 = H; R1 = R2 = indane, trimethyl-bicyclo[2.2.1]heptane), alkyl derived of pyridine N-oxides II, bipyridine N-oxides III, and isoquinoline N-oxides IV, based on amino alcs. R1(NH2)HC-CH(OH)R2 derived from natural amino acids or other previously prepared, is presented herein. Various synthetic pathways have been designed and tested according to the properties and limitations imposed by the target products. The encountered problems related to the stability of the products were discussed. The resulting compounds (eighteen structures) were tested as catalysts in the allylation of benzaldehyde (obtaining up to 79% ee) as well as in nitroaldol reaction (obtaining up to 48% ee).

Catalysts published new progress about Allylation catalysts, stereoselective. 100-70-9 belongs to class nitriles-buliding-blocks, name is Picolinonitrile, and the molecular formula is C6H4N2, SDS of cas: 100-70-9.

Referemce:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts

Lai, Calvine published the artcileAdvances in Stereoselective Iron(II)-Catalyzed Synthesis of Sulfilimines with N-Mesyloxycarbamates, HPLC of Formula: 100-70-9, the main research area is sulfilimine preparation enantioselective diastereoselective; thioether mesyloxycarbamate amination iron catalyst stereoselective.

A stereoselective amination of thioethers R1SR2 to access sulfilimines (R)-R1R2SNC(O)OR3 [R1 = Ph, naphthalen-2-yl, thiophen-2-yl, etc., R2 = Me, Et, R3 = (4-methylphenyl)methyl, diphenylmethyl, 2,2,2-trichloroethyl, etc.] using N-mesyloxycarbamates MsOHNC(O)OR3 in a catalytic system composed of iron(II) chloride and a pyridine oxazoline (PyOX) ligand, e.g., (S)-5,5-dimethyl-4-phenyl-2-(pyridin-2-yl)-4,5-dihydrooxazole, has been developed. The reaction proceeds with modest to good yields and selectivities (up to 86:14 d.r. and 72:28 e.r.). Selectivity was controlled by both the structure of the chiral ligand and the amination reagent.

Helvetica Chimica Acta published new progress about Amination catalysts (stereoselective). 100-70-9 belongs to class nitriles-buliding-blocks, name is Picolinonitrile, and the molecular formula is C6H4N2, HPLC of Formula: 100-70-9.

Referemce:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts

Malancona, Savina published the artcile5,6-Dihydroxypyrimidine Scaffold to Target HIV-1 Nucleocapsid Protein, Recommanded Product: Picolinonitrile, the main research area is dihydroxy pyrimidine derivative preparation HIV1 nucleocapsid protein ADME structure.

The HIV-1 nucleocapsid (NC) protein is a small basic DNA and RNA binding protein that is absolutely necessary for viral replication and thus represents a target of great interest to develop new anti-HIV agents. Moreover, the highly conserved sequence offers the opportunity to escape the drug resistance (DR) that emerged following the highly active antiretroviral therapy (HAART) treatment. On the basis of our previous research, nordihydroguaiaretic acid 1 acts as a NC inhibitor showing moderate antiviral activity and suboptimal drug-like properties due to the presence of the catechol moieties. A bioisosteric catechol replacement approach led us to identify the 5-dihydroxypyrimidine-6-carboxamide substructure as a privileged scaffold of a new class of HIV-1 NC inhibitors. Hit validation efforts led to the identification of optimized analogs, as represented by compound 28, showing improved NC inhibition and antiviral activity as well as good ADME and PK properties.

ACS Medicinal Chemistry Letters published new progress about Anti-HIV agents (anti-HIV-1 agents, Anti-HIV-1 drugs). 100-70-9 belongs to class nitriles-buliding-blocks, name is Picolinonitrile, and the molecular formula is C6H4N2, Recommanded Product: Picolinonitrile.

Referemce:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts

Perevoshchikova, Anna N. published the artcileSynthesis and Prediction of the Ubiquinol-cytochrome c Reductase Inhibitory Activity of 3,4-Dihydroisoquinolines and 2-Azaspiro[4.5]decanes (Spiropyrrolines), SDS of cas: 100-70-9, the main research area is ubiquinol cytochrome c reductase inhibitor hydroisoquinoline azaspirodecane.

Isoquinolines rank as the second largest group among the plant alkaloids. Natural isoquinolines and synthetic isoquinoline derivatives exhibit numerous biol. activities. In this study, the approaches to synthesis of new 3,4-dihydroisoquinoline and 2-azaspiro[4.5]decane (spiropyrroline) derivatives annelated by C(3)-C(4) bonds with a cyclohexyl or cyclopentyl moiety have been developed. In accord with the results of biol. activity prediction by the PASS software, mol. docking was carried out on the ubiquinol-cytochrome c reductase (bc1 complex) model. Compounds 6e and 12a,d (I – III, resp.) were found out as potential Q0 site inhibitors of the bovine bc1 complex.

Journal of Heterocyclic Chemistry published new progress about Drug screening (in silico, using PASS software). 100-70-9 belongs to class nitriles-buliding-blocks, name is Picolinonitrile, and the molecular formula is C6H4N2, SDS of cas: 100-70-9.

Referemce:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts

Ashraf, Muhammad Aqeel published the artcileFe3O4@L-lysine-Pd(0) organic-inorganic hybrid: As a novel heterogeneous magnetic nanocatalyst for chemo and homoselective [2+3] cycloaddition synthesis of 5-substituted 1H-tetrazoles, SDS of cas: 100-70-9, the main research area is tetrazole preparation green chem chemo homoselective; aryl nitrile sodium azide cycloaddition reaction palladium nanocatalyst.

An efficient and sustainable synthetic protocol has been presented to synthesis and 5-substituted 1H-tetrazole privileged heterocyclic substructures I (R = Ph, 4-formylphenyl, pyridin-2-yl, etc.). The synthetic protocol involves two-component reaction between aryl nitriles RCN and NaN3 in water using complex of L-lysine-palladium nanoparticles (NPs) modified Fe3O4 nanoparticles as magnetically separable, recyclable, and reusable heterogeneous catalyst. Magnetically retrievable L-lysine-Pd(0) modified Fe3O4 nanoparticles were applied in [2+3] cycloaddition synthesis of 5-substituted 1H-tetrazoles I. The advantages of this strategy include easy recovery and efficient reusability of the expensive Pd NPs, obtaining high yields of [2+3] cycloaddition and short reaction times, and all of the reported synthetic strategies are being performed in water as green solvent for a wide range of substrates.

Applied Organometallic Chemistry published new progress about [3+2] Cycloaddition reaction (chemoselective). 100-70-9 belongs to class nitriles-buliding-blocks, name is Picolinonitrile, and the molecular formula is C6H4N2, SDS of cas: 100-70-9.

Referemce:
Nitrile – Wikipedia,
Nitriles – Chemistry LibreTexts