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Chalcogen bonded directly to ring carbon of the diazole ring

Subclass of:

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

548000000 - ORGANIC COMPOUNDS (CLASS 532, SUBCLASS 1)

548000000 - 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)

548100000 - Hetero ring is five-membered having two or more ring hetero atoms of which at least one is nitrogen (e.g., selenazoles, etc.)

548356100 - 1,2-diazoles (including hydrogenated)

Patent class list (only not empty are listed)

Deeper subclasses:

Class / Patent application numberDescriptionNumber of patent applications / Date published
548366100 Chalcogen bonded directly to ring carbon of the diazole ring 37
20110207940Preparing 5-fluoro-1-alkyl-3-fluoroalkyl-1H-pyrazole-4-carbonyl chlorides - The present invention relates to a novel process for preparing 5-fluoro-1-alkyl-3-fluoroalkyl-1H-pyrazole-4-carbonyl chlorides, a useful intermediate in the manufacture of fungicides.08-25-2011
20110288304Process for Preparing 1-Alkyl-3-difluoromethyl-5-hydroxypyrazoles - The present invention relates to a process for preparing 1-alkyl-3-difluoromethyl-5-hydroxypyrazoles, which are valuable intermediates for the production of fungicides.11-24-2011
20130131352Process for Preparing 1-phenylpyrazoles - The present invention to a process for preparing 1-phenylpyrazoles of the formula I05-23-2013
20130165664Preparing 5-Fluoro-1-alkyl-3-fluoroalkyl-1H-pyrazole-4-carbaldehydes - The present invention relates to a novel process for preparing 5-fluoro-1-alkyl-3-fluoro-1-alkyl-1H-pyrazole-4-carbonyl chlorides, a useful intermediate in the manufacture of fungicides.06-27-2013
20130253204PYRAZOLE COMPOUNDS HAVING THERAPEUTIC EFFECT ON MULTIPLE MYELOMA - Novel therapeutic agents for myeloma are provided.09-26-2013
548367400 Nitrogen attached directly to the diazole ring by nonionic bonding 15
20110190510Method for Producing and Purifying Trifluoromethanesulfinic Acid - The invention relates to a process for purifying trifluoromethanesulfinic acid by azeotropic distillation with an aromatic solvent, to processes for preparing purified trifluoromethanesulfinic acid and to the use of the purified trifluoronnethanesulfinic acid for preparing trifluoromethylsulfinylated pyrazole derivatives, especially fipronil.08-04-2011
20120184753METHOD FOR THE SYNTHESIS OF 5-AMINO-1-PHENYL-3-CYANO-4-TRIFLUOROMETHYL SULFINYL - The present invention relates to a method for the preparation of the 5-amino-1-phenyl-3-cyano-4-trifluoromethyl sulfinyl pyrazole having the described general formula (I), particularly preferred for the synthesis of Fipronil, through oxidation of a compound having the general formula (II) as follows:07-19-2012
20120215008Process for the Preparation of 4-Sulfinyl-Pyrazole Derivatives - The present invention relates to a novel process for the preparation of a compound of formula (I),08-23-2012
20130030190PROCESS FOR SYNTHESIS FIPRONIL - The present disclosure relates to a process for trifluoromethylsulfinyl pyrazole compound of formula I,01-31-2013
20130197238FIPRONIL PRODUCTION PROCESS - An improved oxidation process for preparing 5-amino-3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-trifluoromethylsulphinyl-pyrazole, of formula (I) is described. The process includes admixing 5-amino-3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-trifluoromethylthiopyrazole of formula (II) with dichloroacetic acid and hydrogen peroxide in the presence of a strong acid.08-01-2013
20140155620FIPRONIL PRODUCTION PROCESS - An improved oxidation process for preparing 5-amino-3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-trifluoromethylsulphinyl-pyrazole, of formula (I) is described. The process includes admixing 5-amino-3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-trifluoromethylthiopyrazole of formula (II) with dichloroacetic acid and hydrogen peroxide in the presence of a strong acid.06-05-2014
20140194630PROCESS FOR SYNTHESIS OF FIPRONIL - A process for preparation of Fipronil (i.e. 5-amino-1-(2, 6-dichloro-4-trifluoromethylphenyl)-3-cyano-4-trifluoro-methylsulphinyl-pyrazole) is provided, which comprises oxidizing 5-amino-1-(2,6-dichloro-4-trifluoromethylphenyl)-3-cyano-4-tri-fluoromethylthio-pyrazole with sulfuric acid and hydrogen peroxide as oxidizing agent in the presence of a solvent such as ethylene dichloride, chlorobenzene.07-10-2014
20150087845PROCESS FOR PREPARATION OF SUBSTITUTED 3'-HYDROAZINO-DIPHENYL-3-CARBOXYLIC ACID COMPOUNDS - The present invention provides a process for the preparation of substituted 3′-hydrazino-biphenyl-3-carboxylic acid compounds. The present invention further provides a process for the preparation of 3′-{N′-[1-(3,4-dimethylphenyl)-3-methyl-5-oxo-1,5-dihydro-pyrazol-4-ylidene]hydrazino}-2′-hydroxybiphenyl-3-carboxylic acid, its intermediate compounds and pharmaceutically acceptable salts thereof.03-26-2015
20150099892FIPRONIL PRODUCTION PROCESS - An improved oxidation process for preparing 5-amino-3-cyano-1-(2,6-dichloro-9-trifluoromethylphenyl)-4-trifluoromethylsulphinyl-pyrazole, of formula (I) is described. The process includes admixing 5-amino-3-cyano-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-trifluoromethylthiopyrazole of formula (II) with dichloroacetic acid and hydrogen peroxide in the presence of a strong acid.04-09-2015
548367700 The nitrogen is multiply bonded to acyclic carbon or is bonded to nitrogen of the diazole ring 2
20080281107Process for the preparation of 5-alkylthioalkylamino-I-phenyl-pyrazoles - The invention relates to a process for the preparation of 5-alkylthioethylamino-1-phenyl-pyrazoles of formula (I) and the preparation of 5-methylamino-1-phenylpyrazole intermediates.11-13-2008
20090030211Process for the Preparation of Fipronil, an Insecticide, and Related Pyrazoles - This invention relates to a process for the preparation of 5-amino-1-phenyl-3-cyano-4-trifluoromethyl sulphinyl pyrazoles as defined by Formula-I,01-29-2009
548368400 Having -C(=X)-, wherein X is chalcogen, bonded directly to the nitrogen 2
20090069571Process for the Preparation of 5-Alkylthioalkylamino-I-Phenyl-Pyrazoles - The invention relates to a process for the preparation of 5-alkylthioethylamino-1-phenyl-pyrazoles of formula (I) and the preparation of 5-methylamino-1-phenylpyrazole intermediates.03-12-2009
20120071666Method for Purifying a Pyrazolinone Derivative - A method for purifying a pyrazolinone derivative comprising a step of mixing a solution containing a mixture containing the pyrazolinone derivative and a good solvent which can dissolve the pyrazolinone derivative with a poor solvent to crystallize the pyrazolinone derivative.03-22-2012
548368700 The nitrogen and the chalcogen are directly bonded to non-adjacent carbons of the diazole ring (e.g., pyrazolone imide or imino pyrazolone, etc.) 1
20130217890METHOD FOR PRODUCING PYRAZOLINONE SALT - A salt represented by formula (4) produced via 08-22-2013
548369100 Chalcogen attached indirectly to the nitrogen by acyclic nonionic bonding 1
20140350267PROCESS FOR THE PREPARATION OF N-SUBSTITUTED PYRAZOLE COMPOUNDS - A process for the preparation of a compound of formula I:11-27-2014
548369400 Having -C(=X)-, wherein X is chalcogen bonded directly to the diazole ring 8
20140012013METHOD FOR PRODUCING PYRAZOLE CARBOXYLIC ACID DERIVATIVE - Disclosed is a process for producing a pyrazole carboxylic acid derivative which is useful as a significant intermediate of an 11βHSD-1 inhibitor.01-09-2014
20140073799THIENOPYRAZOLE DERIVATIVE HAVING PDE7 INHIBITORY ACTIVITY - To provide thienopyrazole derivatives inhibiting PDE 7 selectively, and therefore, enhance cellular cAMP level. Consequently, the compound is useful for treating various kinds of disease such as allergic diseases, inflammatory diseases or immunologic diseases. The compound is thienopyrazole compound represented by the following formula (I):03-13-2014
548369700 Acyclic nitrogen or chalcogen bonded directly to the -C(=X)- group 6
20090018345PYRAZOLE-1-CARBOXYLATE DERIVATIVES, PROCESS FOR THE PRODUCTION THEREOF AND PROCESS FOR THE PRODUCTION OF PYRAZOLE DERIVATIVES - Disclosed are pyrazole-1-carboxylate derivatives of the general formula (1),01-15-2009
20100105923PROCESS FOR PRODUCTION OF HYDROXYADAMANTANEAMINE - Disclosed is a process for producing 1-hydroxy-4-aminoadamantane.04-29-2010
20110269971PROCESS FOR PRODUCTION OF HYDROXYADAMANTANEAMINE - Disclosed is a process for producing 1-hydroxy-4-aminoadamantane.11-03-2011
20120259128ADAMANTANAMINE DERIVATIVE - Disclosed is an adamantanamine derivative which is useful as a significant intermediate of an 11βHSD-1 inhibitor.10-11-2012
20140128616OXYGEN-SUBSTITUTED 3-HETEROAROYLAMINO-PROPIONIC ACID DERIVATIVES AND THEIR USE AS PHARMACEUTICALS - The present invention relates to compounds of the formula I, wherein A, D, E, G, R05-08-2014
20150018561CF3O-CONTAINING ENAMINOKETONES AND THEIR UTILIZATION FOR THE PREPARATION OF CF3O-CONTAINING PYRAZOLES - The present invention pertains to novel enaminoketones containing a CF01-15-2015
548370100 Nitrogen attached indirectly to the diazole ring by acyclic nonionic bonding 2
20130281710PROCESSES FOR THE PREPARATION OF 1-ARYL-5-ALKYL PYRAZOLE COMPOUNDS - Provided are improved processes for the preparation of 1-aryl pyrazole compounds of formula (I) and (IB):10-24-2013
20150073153PROCESSES FOR THE PREPARATION OF 1-ARYL-5-ALKYL PYRAZOLE COMPOUNDS - Provided are improved processes for the preparation of 1-aryl pyrazole compounds of formula (I) and (IB):03-12-2015
548370400 Chalcogen attached indirectly to the diazole ring by acyclic nonionic bonding 2
20090036688Process for Production of 5-Alkoxy-4-Hydroxymethylpyrazole Compound - The present invention relates to a process for producing a 5-alkoxy-4-hydroxymethylpyrazole compound represented by the general formula (3)02-05-2009
20130165665COMPOUNDS ACTING AT MULTIPLE PROSTAGLANDIN RECEPTORS GIVING A GENERAL ANTI-INFLAMMATORY RESPONSE - The present invention provides a compound that is represented by the following general formula06-27-2013
548371100 Benzene ring is bonded directly to ring nitrogen of the diazole ring (e.g., 1-phenyl-3-methyl-5-pyrazolone; antipyrine, etc.) 5
20120165544Process for Preparing 1-Phenylpyrazoles - The present invention to a process for preparing 1-phenylpyrazoles of the formula I in which each R06-28-2012
20130005986N-Carbomethoxy-N-methoxy-(2-chloromethyl)-anilines, their preparation and their use as precursors for preparing 2-(pyrazol-3'-yloxymethylene)-anilides - The present invention relates to N-carbomethoxy-N-methoxy-(2-chloromethyl)-aniline compounds of the formula I, wherein: n is 0, 1, 2 or 3, each R01-03-2013
20130178634Process for Preparing Substituted N-Phenylhydroxylamines - The present invention relates to a process for the preparation of a ring-substituted N-phenylhydroxylamine by reduction of the correspondingly substituted nitrobenzene compound, wherein the reduction is carried out by reacting the substituted nitrobenzene compound with hydrazine in the presence of a ruthenium catalyst.07-11-2013
20130184472Process for the Preparation of 1-ARYL-PYRAZOL-3-ONE Intermediates Useful in the Synthesis of SIGMA Receptors Inhibitors - The invention relates to a process for preparing 1-aryl-pyrazol-3-one intermediates, tautomers, and salts thereof, to novel intermediates, and to the use of the intermediates in the preparation of sigma receptor inhibitors.07-18-2013
20130338373Process for Preparing Substituted N-Phenylhydroxylamines - The present invention relates to a process for the preparation of 2-[[[1-(4-chlorophenyl)-1H-pyrazol-3-yl]oxy]methyl] phenyl]-hydroxylamine from the correspondingly substituted nitrobenzene compound.12-19-2013

Patent applications in all subclasses Chalcogen bonded directly to ring carbon of the diazole ring

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