Patents - stay tuned to the technology

Inventors list

Assignees list

Classification tree browser

Top 100 Inventors

Top 100 Assignees


The hetero ring is five-membered

Subclass of:

549 - Organic compounds -- part of the class 532-570 series

549000000 - ORGANIC COMPOUNDS (CLASS 532, SUBCLASS 1)

549000000 - HETEROCYCLIC CARBON COMPOUNDS CONTAINING A HETERO RING HAVING CHALCOGEN (I.E., OXYGEN, SULFUR, SELENIUM, OR TELLURIUM) OR NITROGEN AS THE ONLY RING HETERO ATOMS (Class 540, subclass 1)

549001000 - Sulfur containing hetero ring (e.g., thiiranes, etc.)

Patent class list (only not empty are listed)

Deeper subclasses:

Class / Patent application numberDescriptionNumber of patent applications / Date published
549041000 Polycyclo ring system having the hetero ring as one of the cyclos 69
549074000 Nitrogen attached indirectly to the hetero ring by nonionic bonding 47
549059000 Additional hetero ring containing 28
549030000 Plural ring hetero atoms in the hetero ring 21
549070000 Having -C(=X)-, wherein X is chalcogen, bonded directly to the hetero ring 17
549078000 Chalcogen attached indirectly to the hetero ring by nonionic bonding 14
549062000 Chalcogen bonded directly to ring carbon of the hetero ring 12
549068000 Nitrogen attached directly to the hetero ring by nonionic bonding 5
20150148550NOVEL COMPOUNDS AS CHLORIDE CHANNEL BLOCKING AGENT - Disclosed is a novel compound to function as a calcium-dependent chloride channel blocking agent.05-28-2015
200900825792-ALKENYL-3-AMINOTHIOPHENE DERIVATIVE AND PROCESS FOR PRODUCING THEREOF - Disclosed is a method for commercially producing 2-alkenyl-3-aminothiophene derivatives, which are useful as intermediates for agricultural chemicals, at low cost. Specifically disclosed is a method for introducing alkenyl groups into the 2-position of 3-aminothiophene derivatives by reacting 3-aminothiophene derivatives represented by the general formula (2) below or salts thereof with a ketone represented by the general formula (1) below without using a protecting group. Also specifically disclosed are 2-alkenyl-3-aminothiophene derivatives (3a) to (3d) which are useful as intermediates for agricultural chemicals,03-26-2009
20090156833Process for the Preparation of Enantiomerically Pure 1-Substituted-3-Aminoalcohols - A process for the preparation of N-monosubstituted β-aminoalcohol sulfonates of formula (Ia), (Ib):06-18-2009
20090326247METHOD FOR PRODUCING 2-ALKYL-3-AMINOTHIOPHENE DERIVATIVE - The present invention provides a method of producing a 2-alkyl-3-aminothiophene derivative represented by formula (2) by reducing at least one of the 2-alkenyl-3-aminothiophene derivatives represented by formulae (1a) to (1d), or a mixture thereof, or a salt thereof, without using a protecting group for an amino group:12-31-2009
20140018548CATALYST FOR ASYMMETRIC HYDROGENATION OF IMINE, SYNTHESIS METHOD AND APPLICATION THEREOF - A chiral hydrogenated H01-16-2014
549061000 Cyano bonded directly to the hetero ring 5
20090082578Process for the synthesis of strontium ranelate and its hydrates - A process for the industrial synthesis of strontium ranelate of formula (I):03-26-2009
20090137822Process for preparing 3-substituted thiophene - The present invention relates to a process for preparing a 3-substituted thiophene represented by the formula (2):05-28-2009
20110275834POLYMORPH OF STRONTIUM RANELATE AND A PROCESS FOR ITS PREPARATION - This invention discloses Strontium Ranelate polymorph, designated as Form A, having a characteristic powdered x-ray diffraction pattern and infrared spectrum with a water content of about 1.5 to 2.5% and a process for its preparation.11-10-2011
20120029210Process for the synthesis of strontium ranelate and its hydrates - Process for the industrial synthesis of strontium ranelate of formula (I):02-02-2012
20130310573PROCESS FOR THE PREPARATION OF STRONTIUM RANELATE - Strontium ranelate is prepared by reacting dicyclohexylammonium ranelate with strontium halide in an anhydrous solvent. Strontium ranelate thus obtained will have less than 3% moisture content.11-21-2013
549087000 Plural chalcogens double bonded directly to ring sulfur of the hetero ring 5
20090005578HIGH SHEAR PROCESS FOR THE PRODUCTION OF BUTADIENE SULFONE - Use of a high shear mechanical device incorporated into a process for the production of sulfolene as a reactor device is capable of decreasing mass transfer limitations, thereby enhancing the sulfolene production process. A system for the production of sulfolene from butadiene and sulfur dioxide, the system comprising a reactor and an external high shear mixer the outlet of which is fluidly connected to the inlet of the reactor; the high shear mixer capable of providing a dispersion of sulfur dioxide gas bubbles within a liquid, the bubbles having an average bubble diameter of less than about 100 μm.01-01-2009
20110288307METHOD FOR MANUFACTURING SULFOLENE COMPOUND AND METHOD FOR MANUFACTURING SULFOLANE COMPOUND - An object of the present invention is to provide a method for manufacturing a sulfolene compound, the method being capable of inhibiting generation of polymers. Another object of the present invention is to provide a method for manufacturing a sulfolane compound, the method being capable of controlling inhibition of hydrogenation catalyst activity and smoothly hydrogenating a sulfolene compound.11-24-2011
20120165551Process and Apparatus for Online Rejuvenation of Contaminated Sulfolane Solvent - A continuous online process for rejuvenating whole stream of contaminated lean sulfolane in an extraction system is provided. A rejuvenator is installed in the solvent circulation loop to remove the contaminants continuously to keep the solvent clean, effective and less corrosive. The rejuvenator includes a high pressure vessel with a removable cover and a round rack with vertical stainless steel tubes fitted in the high pressure vessel. A magnetic bar is placed in each stainless steel tube. A screen cylinder is installed outside the ring of stainless steel tubes. As the contaminated sulfolane is passed through the rejuvenator, the rejuvenator picks up contaminants. The rejuvenator can be dissembled to remove the contaminants periodically. The rejuvenator is simple in construction, reliable in operation, and low in operation and maintenance costs. With this rejuvenator, the extraction system operates at high efficiency and high capacity without the dreaded corrosion.06-28-2012
20130225838Regeneration of Selective Solvents for Extractive Processes - Recovering a polar hydrocarbon (HC) selective solvent substantially free of hydrocarbons (HCs) and other impurities from a lean solvent stream containing the selective solvent, measurable amounts of heavy aromatic HCs, and polymeric materials that are generated in an extractive distillation (ED) or liquid-liquid extraction (LLE) process. At least a portion of the lean solvent stream is contact in a solvent clean-up zone with a slip stream from the HC feed stream of the ED or LLE process or an external stream. The HC feed stream, such as pyrolysis gasoline or reformate, contains significant amounts of benzene and at least 50% polar (aromatic) HCs and serves as a displacement agent to remove the heavy HCs and polymeric material from the lean solvent stream. A magnetic filter can be used to remove the paramagnetic contaminants from the lean solvent.08-29-2013
20160376250BUTADIENE SEQUESTRATION VIA SULFUR DIOXIDE CHARGED ZEOLITE BEDS - In an example, a method of butadiene sequestration includes receiving an input stream that includes butadiene. The method includes directing the input stream to a first sulfur dioxide charged zeolite bed for butadiene sequestration via a first chemical reaction of butadiene and sulfur dioxide to form sulfolene.12-29-2016
549083000 The compound consists of the ring sulfur, carbon, and hydrogen 2
20100217015Process for the preparation of substituted heteroaromatics - A process is described for the preparation of substituted heteroaromatics of the general formula (I)08-26-2010
20140012018SULFOLANE COMPOSITION - The present invention aims to provide, with combination of a sulfolane compound and an organic alkanolamine compound, a sulfolane composition which is not likely to cause odor, can suppress pyrolysis of the sulfolane compound with a reduced amount of additives, and can reduce generation of sulfur dioxide. The present invention relates to a sulfolane composition containing a sulfolane compound represented by formula (1) and an organic alkanolamine compound, wherein R01-09-2014
549081000 Halogen attached directly to the hetero ring by nonionic bonding 1
20090259053PROCESS FOR BROMINATING ALKYLTHIOPHENES - What is described is a process for brominating alkylthiophene, in which an alkylthiophene of the general formula (I)10-15-2009
549080000 Unsaturated carbocyclic ring or acyclic carbon to carbon unsaturation containing 1
20100004467COMPOUNDS COMPRISING A LINEAR SERIES OF FIVE FUSED CARBON RINGS, AND PREPARATION THEREOF - The present application discloses methods for the production of organic compounds comprising a linear series of five fused carbon rings. Such compounds are useful in the production of electronic components, devices and materials. For example the methods disclosed permit the production of 2,9- and 2,10-disubstituted pentacene compounds and 2,6,9,13- and 2,6,10,13-tetrasubstituted compounds that present particularly advantageous properties for the manufacture of semiconductor materials, and may be used in devices such as for example thin film transistors and solar cells. These features are enhanced by π-π parallel stacking in the solid state. Also disclosed are compounds that are excellent candidates for use in the manufacture of semiconductor materials, and other components of electronic systems, by virtue of their solubility, crystal packing geometries, and electronic properties.01-07-2010
Entries
DocumentTitleDate
20080319207ORGANIC PHOTOVOLTAIC DEVICES COMPRISING FULLERENES AND DERIVATIVES THEREOF - Photovoltaic cells comprising an active layer comprising, as p-type material, conjugated polymers such as polythiophene and regioregular polythiophene, and as n-type material at least one fullerene derivative. The fullerene derivative can be C60, C70, or C84. The fullerene also can be functionalized with indene groups. Improved efficiency can be achieved.12-25-2008
20090069577Silicon-Based Cross-Coupling Reagent and Production Method of Organic Compound Using the Same - In one embodiment of the present invention, a silicon-based cross-coupling reagent is disclosed which is a highly stable tetraorganosilicon compound allowing for a cross-coupling reaction under mild reaction conditions without using fluoride ions, transition metal promoter, or strong bases, and the residue of the silicon reagent can be recovered and reused. The silicon-based cross-coupling reagent is a silicon compound in which an o-hydroxymethylphenyl group is connected to a silicon atom for intramolecular activation.03-12-2009
20090176994ORGANIC PHOTOVOLTAIC DEVICES COMPRISING FULLERENES AND DERIVATIVES THEREOF AND IMPROVED METHODS OF MAKING FULLERENE DERIVATIVES - Improved methods of fullerene derivative production including use of less solvent, or elimination of solvent, as well as use of shorter reaction times and higher reaction temperatures. Methods useful for production of bis-, tris-, tetra-, penta-, and hexa-fullerene derivatives. Indene is a preferred derivative. The derivatives used in active layers for solar cell applications.07-09-2009

Patent applications in all subclasses The hetero ring is five-membered

Website © 2025 Advameg, Inc.