1546 results about "Pyridine" patented technology

The invention relates to the field of preparation of polyurethane damping materials, in particular to a preparation method of a repairable polyurethane damping material based on multiple hydrogen bonds and metal coordination. Compared with a traditional damping material, the damping material has a higher damping temperature range and has a good damping effect at the temperature of-20 DEG C to 60 DEG C. Multiple reversible hydrogen bonds are introduced through diamine containing amido bonds, the material is endowed with self-repairing and high mechanical strength, and damping and self-repairing performance is further enhanced through pyridine nitrogen atom metal coordination. Starting from molecular structure design, multiple hydrogen bonds and metal-ligand coordination bonds constructed on a polyurethane molecular main chain play a role in synergistic enhancement, energy can be effectively dissipated through dissociation and recombination of the multiple hydrogen bonds and fracture and association of the metal coordination bonds, and the energy consumption is reduced. The polyurethane material is endowed with excellent damping performance and self-healing capability by the dual dynamic action.

The present disclosure relates to an improved, efficient, scalable process to prepare intermediate compounds, such as 2-isopropyl-4-methylpyridin-3-amine, useful for the synthesis of compounds, such as Compound 9, for the treatment of KRAS G12C mutated cancers.

The invention discloses a preparation method of an ultra-pure hydroxylamine aqueous solution, and relates to the field of organic chemistry and chemical industry production. The method comprises the following steps: reacting electronic-grade hydroxylamine salt with organic alkali in a proper solvent to generate hydroxylamine, then separating and removing salt and unreacted hydroxylamine in a reaction solution through a mercaptopyridine ion exchange modified membrane, and finally concentrating the solution into 50wt% ultra-high-purity hydroxylamine aqueous solution by adopting reduced pressure evaporation or multi-effect evaporation. The process has the characteristics of high efficiency, environmental protection, simplicity and easiness in operation, effectively improves the purity, yield and separation efficiency of hydroxylamine, and meets the strict requirements of electronic grade hydroxylamine on purity and metal ion content.

The invention discloses a copper surface micro-etching coarsening solution for a fine circuit as well as a preparation method and application of the copper surface micro-etching coarsening solution, and relates to the technical field of printed circuit board manufacturing. The copper surface micro-etching coarsening solution for the fine circuit is prepared from, by mass concentration, 60 g / L to 100 g / L of sulfuric acid, 40 g / L to 60 g / L of hydrogen peroxide, 0.5 g / L to 2 g / L of zinc sulfate, 10 g / L to 30 g / L of copper ions, 0.5 g / L to 1 g / L of pyridine heterocycle-containing Schiff base, 10 g / L to 100 g / L of ethyl alcohol, 1 g / L to 3 g / L of 2-mercaptobenzothiazole, 1 g / L to 5 g / L of methionine and 1 g / L to 5 g / L of polyacrylamide. According to the copper surface micro-etching coarsening solution, the 2-mercaptobenzothiazole and the methionine in the copper surface micro-etching coarsening solution can enable the copper surface to form a honeycomb structure under the low micro-etching amount, the zinc sulfate and the pyridine heterocyclic ring-containing Schiff base can form a composite film layer with copper ions on the surface of the honeycomb structure, and the interlayer binding force is improved.

The invention discloses a preparation method of 5-hydroxy-3-iminopyridine-2, 6-diketone, and relates to the technical field of compound preparation. The invention provides a preparation method of 5-hydroxy-3-iminopyridine-2, 6-diketone, which comprises the following steps: uniformly mixing observation blue with at least one oxidant of sodium hypochlorite, potassium permanganate and hydrogen peroxide according to a molar ratio of 1: (0.5-1.5) under a solution condition, reacting for 5-120 minutes, and adding a reducing agent to finish the reaction, thereby obtaining a target product. According to the preparation method provided by the invention, on the basis of the amide structure of the ornamental blue, 'endogenous catalysis' of the reaction can be realized, no additional catalyst needs to be introduced, and the 5-hydroxy-3-iminopyridine-2, 6-diketone with the yield of more than 60.53% and the purity of more than 60.2% can be prepared through a simple and convenient one-step reaction.

This invention relates to the field of pharmaceutical technology, specifically to a substituted pyridotriazole compound, its preparation method, and its uses. This specification discloses a substituted pyridotriazole compound that inhibits RIPK1 and / or MLK, as well as its pharmaceutically acceptable salts, stereoisomers, solvent compounds, or prodrugs. The compound is shown in formula (I), where the definitions of each group are detailed in the specification. Furthermore, this invention also discloses pharmaceutical compositions comprising this compound and their use in the preparation of medicaments for treating RIPK1-related diseases or conditions.

The invention relates to an oil-soluble viscosity reducer composition and a preparation method and application thereof.The oil-soluble viscosity reducer composition is formed by compounding alkyl pyridine and coker diesel oil and can rapidly permeate into thick oil, the viscosity of the thick oil is greatly reduced, and the fluidity of the thick oil is improved. When the oil-soluble viscosity reducer is used in heavy oil reservoir exploitation, storage and transportation processes, the use amount of thin oil for blending heavy oil with thin oil can be saved, the cost of the oil-soluble viscosity reducer is reduced, efficient exploitation, gathering and transportation of the heavy oil reservoir are guaranteed, cost-reducing and efficiency-increasing exploitation of the heavy oil reservoir is realized, and high-added-value comprehensive utilization of coker diesel oil is facilitated.

The present disclosure is directed to a preservative composition comprising a linear polyetheramine having a molecular weight greater than 118 Daltons (Da) and at least one isothiazolinone, whereby this preservative composition may further comprise a pyrithione salt and / or a metal salt. Also disclosed is an aqueous industrial material comprising the preservative composition as well as a method for enhancing in-contaniner preservative performance of an aqueous industrial material using the preservative composition.

The present disclosure relates to an improved, efficient, scalable process to prepare intermediate compounds, such as 2-isopropyl-4-methylpyridin-3-amine, useful for the synthesis of compounds, such as Compound 9, for the treatment of KRAS G12C mutated cancers.

The present invention provides compounds of formula I for the treatment of diseases such as systemic lupus erythematosus, systemic sclerosis (SSc), interferonosis, nonalcoholic steatohepatitis (NASH), interstitial lung disease (ILD), and idiopathic pulmonary fibrosis (IPF). JPEG2026504613000125.jpg8493 (in the formula, R 1 , R 2 , R 3 , R 4 , A, D, E, G, J, K, and L are as defined in claim 1), and prodrugs, deuterated analogs, and pharmaceutically acceptable salts thereof.

The invention provides a nitrogen modified iron-cobalt bimetallic catalyst as well as a preparation method and application thereof, and belongs to the technical field of catalysts. The catalyst takes iron and cobalt as active components, and is prepared by adopting a coprecipitation-hydrothermal-step atmosphere heat treatment process: firstly, carrying out coprecipitation reaction on iron salt and cobalt salt, controlling the pH value to be 11 + / -0.5, carrying out aging and hydrothermal treatment, filtering, washing, drying and grinding to obtain a precursor; and calcining the precursor in a hydrogen-containing mixed atmosphere at 400-500 DEG C, and then calcining the precursor in an ammonia-containing mixed atmosphere at 450-600 DEG C to obtain the nitrogen surface modified iron-cobalt bimetallic catalyst. The catalyst is of a carrier-free iron-cobalt bimetallic structure, nitrogen atoms are embedded into alloy lattices or adsorbed on the surface in the form of pyridine nitrogen, pyrrole nitrogen or graphite nitrogen, and a Fe / Co-N high-activity interface is formed.

A carbon sorbent for removing carbon dioxide from a gaseous material includes a surface composition including carbon, nitrogen, and oxygen. The nitrogen atoms at the surface of the carbon sorbent may be present in pyridone, pyrrole, and pyridine. The surface of the carbon sorbent may include lactone groups and pyrone groups. The carbon sorbent may have a bulk density greater than about 0.40 grams per cubic centimeter. The carbon sorbent may be formed using amino acids to provide the nitrogen for the carbon sorbent. In addition, the use of processing aids during the formation of the carbon sorbent facilitates the formation of a denser carbon sorbent. Related methods of forming the carbon sorbent and pellets of the carbon sorbent are also disclosed.

The invention discloses a pyridine quaternized cellulose derivative and a preparation method thereof, and belongs to the field of modified cellulose derivatives. According to the method, sodium carboxymethyl cellulose is taken as a raw material, and a target product is prepared through a three-step method of epoxy group grafting, sulfydryl-epoxy click chemical reaction and pyridine quaternization reaction in sequence. According to the method, the high efficiency of click chemistry and the modular design concept are innovatively introduced into the field of cellulose derivative modification, the problems that a traditional quaternization method is uncontrollable in substitution degree, many in side reaction and poor in molecular design flexibility are solved, and the method has the advantages of being mild in reaction condition, high in efficiency and clear in product structure.

The invention belongs to the technical field of preparation of transition metal organic photocatalysts, and particularly relates to design and a preparation method of a carbazole terpyridyl nickel catalyst. The invention aims to design and synthesize a carbazole terpyridyl nickel catalyst with light / nickel synergistic catalytic activity. The preparation method comprises the following specific synthesis steps: reacting different types of alpha-pyridone pyridinium and alpha, beta-unsaturated ketone in methanol, and carrying out suction filtration, washing, drying and other operations to obtain the corresponding carbazole terpyridyl ligand. The carbazole terpyridyl ligand and anhydrous nickel bromide are subjected to a heating reflux reaction in a tetrahydrofuran solution, and the corresponding carbazole terpyridyl nickel catalyst is obtained through methanol washing, suction filtration, drying and other operations. The terpyridyl nickel catalyst has high catalytic activity in a C-N, C-O and C-S coupling reaction promoted by visible light.

A carbon sorbent for removing carbon dioxide from a gaseous material includes a surface composition including carbon, nitrogen, and oxygen. The nitrogen atoms at the surface of the carbon sorbent may be present in pyridone, pyrrole, and pyridine. The surface of the carbon sorbent may include lactone groups and pyrone groups. The carbon sorbent may have a bulk density greater than about 0.40 grams per cubic centimeter and may exhibit a carbon dioxide capacity of at least 11.0 weight percent at 30° C. and 760 mmHg. The carbon sorbent may be formed using amino acids to provide the nitrogen for the carbon sorbent. In addition, the use of processing aids during the formation of the carbon sorbent facilitates the formation of a denser carbon sorbent. Related methods of forming the carbon sorbent and pellets of the carbon sorbent are also disclosed.

The application provides an acid ester composite diesel anti-wear agent and a preparation method thereof, and belongs to the technical field of diesel additives, and comprises the following steps: S1, preparing a silanized solid acid catalyst; S2, preparing C18 polyol ester; S3, mixing an acid type anti-wear component and the C18 polyol ester, and then stirring after heating, and then adding tetrahydropyrazole pyridine derivatives and a diluent to continue stirring, and then cooling and filtering to obtain the acid ester composite diesel anti-wear agent. The application can improve the lubricity and anti-wear performance of low-sulfur diesel at a lower additive dosage, and has low corrosion and good oxidation stability.

The present disclosure relates to heterocyclyl pyridazine compounds, processes and intermediates for their preparation as well as the uses thereof for controlling phytopathogenic microorganisms, such as phytopathogenic fungi.

The invention discloses an MOF / nitrogen-doped graphene-based electrocatalyst and a preparation method thereof, nitrogen-doped graphene has a single nitrogen configuration, and the nitrogen-doped graphene is pyridine nitrogen or pyrrole nitrogen; the MOF is ZIF-67, and the MOF is connected with a nitrogen atom of the nitrogen-doped graphene through a coordinate bond. Carrying out covalent functionalization on the surface of the graphene by using a specific pyridine nitrogen configuration polymer; then growing MOF in situ by taking the nitrogen-doped graphene as a precursor, and then calcining to realize the compounding of the nitrogen-doped graphene with the single nitrogen configuration and the MOF. According to the prepared MOF / nitrogen-doped graphene composite electrocatalyst, the stability and the electrocatalytic activity (such as OER, HER and ORR) of MOF can be remarkably improved. Meanwhile, the preparation method is simple in process, low in cost and remarkable in industrial application potential.

The invention discloses an aggregation-induced emission photosensitizer as well as a preparation method and application thereof. A D-A-pi-A-D symmetrical structure is adopted, the spatial effect and the conjugation degree are adjusted through a pi bridge, the molar absorption coefficient is increased, and singlet excitons are increased; and furthermore, a pyridine ring with positive charges is used for accelerating electron transfer, the yield of triplet excitons and ROS is improved, compared with a traditional photosensitizer, the ROS efficiency is improved by 2-3 times, the efficient killing capability of the photosensitizer on pathogens can be ensured, and a guarantee is provided for rapid healing of infectious wounds. A pyridine ring with positive charges is introduced into an MTCNPy molecule, and the targeting property of the photosensitizer to pathogens is enhanced by utilizing the electrostatic interaction between the pyridine ring and a bacterial negative charge cell membrane, so that the damage to surrounding healthy tissues is reduced. The preparation process is simple, the cost is low, and the hydrogel has excellent hydrophilicity and biocompatibility so as to be more suitable for the biological environment.

The invention provides a diesel oil anti-wear agent and a preparation process thereof, and belongs to the technical field of diesel oil additives, and the preparation process comprises the following steps: mixing and stirring diisooctyl maleate and xylene, adding diethylenetriamine and deionized water, carrying out heating reaction, adding toluene, 4-(aminomethyl) pyridine and ethylene oxide, carrying out mixing reaction, filtering, washing, and drying to obtain the diesel oil anti-wear agent. The pyridinium-based polyester hollow capsule is prepared; the preparation method comprises the following steps: mixing xylene, catechol, ethylene phosphonic acid, ammonium persulfate and deionized water, heating, dispersing in cyclohexane, adding polyvinyl alcohol, octadecyl methacrylate and azodiisobutyronitrile, mixing and reacting to obtain catechol phosphonate nano colloidal particles; mixing and stirring the fatty acid ester solution, the oleoyl fluorocarbon copolymer and the pyridinium-based polyester hollow capsule, adding the catechol phosphonate nano colloidal particles, continuously stirring, performing ultrasonic treatment, and degassing to obtain the diesel oil anti-wear agent. The diesel oil antiwear agent can improve the antiwear property and demulsibility of the diesel oil antiwear agent.

The invention provides a reactive dye with a high fixation rate and a preparation method thereof. The reactive dye is prepared from the following raw materials in parts by mass: 25 parts of modified reactive dye, 0.3-0.7 part of a metal ion agent and 60-80 parts of water, wherein the modified reactive dye is obtained by inclusion of reactive dye molecules with beta-cyclodextrin-pyridine carboxylic acid, and beta-cyclodextrin and pyridine carboxylic acid in the beta-cyclodextrin-pyridine carboxylic acid are connected through an alkyl chain; metal ions provided by the metal ion agent can be chelated with the picolinic acid. Reactive dye molecules and beta-cyclodextrin-pyridine carboxylic acid form an inclusion structure, the hydrolysis probability of active groups is reduced, and an alkyl chain regulates steric hindrance and molecular spacing, so that pyridine nitrogen and carboxylic acid more efficiently form a more stable chelate with metal ions and further form coordinate bonds with hydroxyl groups on the fiber surface, and the fixation rate of the reactive dye is improved.

To provide an excellent pest control agent composition that contains a novel agent having a pest control effect and a known pest control agent.SOLUTION: A pest control agent composition prepared by mixing an active ingredient A selected from the group consisting of aryl tetrahydropyridine compounds represented by formula (1) with a known pest control agent. [Q represents Q-1 or the like, Z1 represents a halogen atom, J represents J-1 or the like, A1 represents N, R1 represents a halogen atom or the like, G represents G-1 or the like, Z2 represents a halogen atom or the like, R2 and R3 represent H, X and Y represent O, t4 represents an integer of 0, 1, 2, 3 or 4, and t5 represents an integer of 0, 1, 2, 3, 4 or 5].SELECTED DRAWING: None

A novel salt form of Compound (I) represented by the following structural formula, and its corresponding pharmaceutical compositions, are disclosed.Particular single crystalline forms of 1:1 Compound (I) tartrate salt are characterized by a variety of properties and physical measurements. Methods of preparing specific crystalline forms are also disclosed. The present disclosure also provides methods of treating cancer in a subject.

The invention discloses an indium-based metal-organic framework material based on a pyridine hexacarboxylic acid ligand as well as a preparation method and application of the indium-based metal-organic framework material, the chemical formula is {[NH2Me2] 2 [In4 (mu2-O) (H6L) 2 (H2O) 2]. 3DMF. 10H2O} n, and H6L is an organic ligand 4, 4 ', 4' '-(pyridine-2, 4, 6-triyl) triisophthalic acid. The material has excellent thermal stability and chemical stability, and due to the frame charge characteristic and the excellent pore structure of the material, the metal organic frame material shows efficient dye selective adsorption and separation performance, can selectively adsorb cationic dye methylene blue MB and repel anionic dye methyl orange MO at the same time. In conclusion, a new design thought is developed for the novel indium-based metal organic framework material based on the pyridine hexacarboxylic acid ligand, and meanwhile, a new candidate is provided for developing a high-efficiency dye wastewater purification material.

The invention relates to a polyion liquid modified polyamide material and a preparation method thereof. The polyamide material provided by the invention comprises a polyionic liquid synergist which comprises an ionic liquid polymer with a synergistic flame-retardant function and specifically comprises one or more of the following components: quaternary ammonium type dihydric phosphate polyionic liquid, imidazole type dihydric phosphate polyionic liquid and pyridine type dihydric phosphate polyionic liquid. The polyamide material provided by the invention can realize excellent flame retardant property, significantly reduce precipitation of the flame retardant and maintain excellent mechanical properties.

The invention relates to a low-alignment-angle high-heat-resistance release film base film for a polaroid and a preparation method thereof, and the release film base film is prepared by taking an optical-grade PET slice as a main body material, adding modified PET and modified SiO2 filler with a specific structure, and carrying out co-extrusion casting and a unique three-section stretching process. According to the modified PET, a 2-(pyridine-3-yl) terephthalic acid comonomer and ionic liquid intercalated montmorillonite are introduced, so that the rigidity and heat resistance of a molecular chain are improved, and a heterogeneous nucleation point is provided; the surface of the modified SiO2 filler is grafted with a terpolymer, so that good compatibility with a matrix and internal lubrication are realized; according to the preparation method, a transverse-longitudinal-transverse three-section stretching sequence and step-by-step increasing temperature control are adopted to cooperatively regulate and control orientation and crystallization of molecular chains; and finally, the optical-grade polyester film with low alignment angle, low transverse thermal shrinkage rate and high surface adhesion is prepared, and is particularly suitable for being used as a release film of a high-end polaroid.

The invention discloses water-soluble nylon glue and a preparation method thereof, and relates to the technical field of water-soluble glue. The preparation method comprises the following steps: preparing a water-soluble polyamide solution from sodium 5-sulfoisophthalate, polyether amine, N-methyl pyrrolidone, pyridine, an antioxidant and an auxiliary agent, adding an inorganic filler, a film-forming agent, a wetting agent and a thickening agent into the water-soluble polyamide solution serving as a base material, and preparing the water-soluble nylon glue under the conditions of heating and high-speed dispersion. The adhesive has the characteristics of good water solubility, high bonding strength and environmental friendliness.

The application discloses a P450 enzyme mutant for degrading herbicides and application thereof, and the P450 enzyme mutant is named P450 BSβ -F46A, P450 BSβ -F46A-CPR; the amino acid sequences are shown in SEQ ID NO. 2 and 4 respectively. The application also discloses application of the P450 enzyme mutant in degrading pyridine oxycarboxylic acid herbicides or aryloxyphenoxypropionic acid herbicides and related genes in cultivating herbicide-resistant transgenic crops. Experiments prove that the highest conversion rate of the P450 enzyme mutant for degrading pyridine oxycarboxylic acid herbicides reaches 86%, and the total conversion number of catalyzing flumiclorac can reach 7443 at most, and the highest catalytic conversion rate of degrading aryloxyphenoxypropionic acid herbicides reaches 89%. The P450 enzyme mutant provided by the application has the advantages of high catalytic efficiency, high protein expression amount and low industrial cost, and the whole operation process for degrading herbicides is simple, the process is mature, the cost is low, and the application prospect is wide.

This invention relates to aggregation-induced emission probes with specific responses to tumor markers and their applications, belonging to the field of biochemistry. This invention utilizes molecular structure modulation to prepare a series of molecules possessing large Stokes shifts, resistance to photobleaching, near-infrared II (NIR-II) emission, and aggregation-induced emission properties. Different self-eliminating groups are attached to the dimethylamino group of the molecule via quaternization or to the pyridine group via pyridinium salting. By controlling the structure of these self-eliminating groups, activatable luminescent probes responding to different tumor markers can be constructed. These probes integrate deep NIR-II imaging, aggregation-point luminescence, large Stokes shifts, and marker-specific responses, providing a new approach for precise imaging diagnosis of tumors.