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Class 564/316 - Amino nitrogen attached to the carbon by an acyclic carbon or chain


Subclass of Class 564 - Organic compounds -- part of the class 532-570 series
Definition: Compounds wherein an amino nitrogen is indirectly bonded
No. of patents: 87
Last issue date: 10/18/2011


1      
NumberTitleIssue Date
8039672Method of obtaining 3,3-diphenylpropylamines
The invention relates to a method of obtaining 3,3-diphenylpropylamines (I), wherein R1 is H, alkyl, haloalkyl or alkoxyalkyl, R2 is alkyl, alkoxy, halogen, NO2, CN, CHO, which may be free or protected, CH2OH or COOR6...
10/18/2011
7538249Tolterodine, compositions and uses thereof, and preparation of the same
Racemic tolterodine free base in crystalline form, tolterodine with improved purity, compositions and uses thereof, and processes of preparing the same. ...
05/26/2009
7462742In situ or one-pot hydrogenation and reductive amination process
An in situ or one-pot process for the preparation of the compounds of formula (I) uses a compound of general formula (I): and includes: a) the hydrogenation of a nitrile group of the compound of general formula (II):
12/09/2008
7420091Process for the preparation of tolterodine
A novel process for the preparation of tolterodine, i.e. (R)—N, N-diisopropyl-3-(2-hydroxy-5-methylphenyl)-3-phenylpropanamine, in the racemic form, as well as intermediates useful for its preparation. ...
09/02/2008
7393874Polymorphs of tolterodine tartrate
The present invention relates to novel polymorphs of tolterodine tartrate, to processes for their preparation and to pharmaceutical compositions containing them. ...
07/01/2008
7358399Process for the preparation of N,N-diisopropyl-3-(2-hydroxy-5-methylphenyl)-3-phenyl-propaneamine
A process is described for the preparation of N,N-diisopropyl-3-(2-hydroxy-5-methylphenyl)-3-phenyl-propaneamine comprising substitution of the sulfonyloxy group of the compound of the formula in which the substituents R an...
04/15/2008
7355079Thyronamine derivatives and analogs and methods of use thereof
Thyronamine derivatives and analogs, methods of using such compounds, and pharmaceutical compositions containing them are disclosed. Methods of preparing such compounds are also disclosed. ...
04/08/2008
7355077Process for preparing tolterodine
A process for preparing tolterodine with high purity. ...
04/08/2008
7339079Thyronamine derivatives and analogs and methods of use thereof
Thyronamine derivatives and analogs, methods of using such compounds, and pharmaceutical compositions containing them are disclosed. Methods of preparing such compounds are also disclosed. ...
03/04/2008
7335793Process for the preparation of tolterodine
A novel process prepares tolterodine, i.e. (R)-N,N-diisopropyl-3-(2-hydroxy-5-methylphenyl)-3-phenylpropanamine, in the racemic form, as well as intermediates useful for its preparation. Tolterodine free base may be prepared by reacting diisopropyl-(3-phenyl-3-p-tol...
02/26/2008
7321065Thyronamine derivatives and analogs and methods of use thereof
Thyronamine derivatives and analogs, methods of using such compounds, and pharmaceutical compositions containing them are disclosed. Methods of preparing such compounds are also disclosed. ...
01/22/2008
72916483,3-diphenylpropylamines useful in therapy
Novel 3,3-diphenylpropylamines of the formula and stereoisomers and physiologically acceptable acid addition salt thereof; wherein R1, R2, R3, R4, R5, and R
11/06/2007
7268166Compounds active at a novel site on receptor-operated calcium channels useful for treatment of neurological disorders and diseases
Method and compositions for treating a patient having a neurological disease or disorder, such as stroke, head trauma, spinal cord injury, spinal cord ischemia, ischemia- or hypoxia-induced nerve cell damage, epilepsy, anxiety, neuropsychiatric or cognitive deficits...
09/11/2007
7268257Process for producing tolterodine
The present invention provides a process for producing tolterodine of the formula (1) or its salt, which comprises a step reacting a compound of the formula (2) with a base to obtain a reaction product; a step reacting the reaction product with a compound of the for...
09/11/2007
7230030Derivatives of 3,3-diphenylpropylamines
The invention concerns novel derivatives of 3,3-diphenylpropylamines, methods for their preparation, pharmaceutical compositions containing the novel compounds, and the use of the compounds for preparing drugs. More particularly, the invention relates to novel prodr...
06/12/2007
RE396673,3-Diphenylpropylamines, their use and preparation
The invention relates to 3,3-diphenylpropylamines of formula (I), wherein R1 signifies hydrogen or methyl, R2 and R3 independently signify hydrogen, methyl, methoxy, hydroxy, carbamoyl, sulphamoyl or halogen, and X represents a terti...
05/29/2007
7141696Smooth muscle spasmolytic agents
The present invention relates to smooth muscle spasmolytic agents, pharmaceutical compositions containing them and method of using said compounds and compositions for the treatment of urinary incontinence, and other smooth muscle contractility conditions. More parti...
11/28/2006
7126028Process for preparing chiral compounds
Process for the preparation of chiral compounds of formula (I) comprising contacting a compound of formula (II) with a source of hydrogen or halide; wherein A is a chiral center; X is selected from oxygen, sulphur and nitrogen; n is selected from 0 and 1 and is equa...
10/24/2006
71191213,3-diphenylpropylamines useful in therapy
Novel 3,3-diphenylpropylamines of the formula and stereoisomers and physiologically acceptable acid addition salt thereof; wherein R1, R2, R3, R4, R5, and R
10/10/2006
7119212Process for the preparation of tolterodine and intermediates thereof
A process for the preparation of 6-methyl-4-(R)-phenyl-chroman-2-one and 6-methyl-4-(S)-phenyl-chroman-2-one, intermediates for the synthesis of tolterodine and its (S) enantiomer, by reaction of 6-methyl-coumarin with phenylboronic acids, esters and derivatives the...
10/10/2006
7078567Amination process
The present invention provides methodology for carbon-nitrogen bond formation via vinyl or aryl amination. In the process of the invention, an sp2 hybridized radical is reacted with an azomethine moiety to form pyrrolidine and indole compounds. The method...
07/18/2006
7045661Crystalline forms of venlafaxine hydrochloride
Crystalline forms of Venlafaxine hydrochloride were found, referred to hereinafter as polymorphic Forms A, B and D. Furthermore, the present invention is directed to processes for the preparation of these crystalline forms and pharmaceutical compositions comprising ...
05/16/2006
7030164Crystalline polymorph of venlafaxine hydrochloride and methods for the preparation thereof
This invention relates to a highly thermally stable novel anhydrous crystalline polymorphic form of venlafaxine hydrochloride, methods for the preparation thereof, and its use. ...
04/18/2006
6906087Crystalline forms of venlafaxine hydrochloride
Crystalline forms of Venlafaxine hydrochloride were found, referred to hereinafter as polymorphic Forms A, B and D. Furthermore, the present invention is directed to processes for the preparation of these crystalline forms and pharmaceutical compositions comprising ...
06/14/2005
6822119Process for the preparation of tolterodine
The present invention relates to a cost effective and industrially advantageous process for the preparation of tolterodine and pharmaceutically acceptable salts thereof. ...
11/23/2004
6759435Antidepressant drugs and methods
Novel amines are potent and selective serotonin reuptake inhibitors and as such can be used in the treatment of depression and other mental disorders. ...
07/06/2004
6713464Derivatives of 3,3-diphenylpropylamines
The invention concerns novel derivatives of 3,3-diphenylpropylamines, methods for their preparation, pharmaceutical compositions containing the novel compounds, and the use of the compounds for preparing drugs. More particularly, the invention relates to novel prodr...
03/30/2004
6518314Pharmaceutical agents that impede the initiation and progression of primary and secondary DMS disruptions
Compositions comprising a pharmaceutically effective amount of a compound that impedes disruption of intact dense microspheres (DMS) by acting on DMS either to prevent disruption, or if disrupted, act on pre-disrupted DMS in such a way that, when the comp...
02/11/2003
6441244Benzophenones and the use thereof as photoinitiators
The invention relates to new compounds of the formula (I) ##STR1## in which R is phenyl, C1-4 alkyl-, C1-4 alkoxy- or halogen-substituted phenyl, naphthyl or an aromatic ring containing heteroatoms; X is O or S; R1 and R2
08/27/2002
6440440Biocidal benzylbiphenyl derivatives
This invention concerns compounds of formula. ##STR1## stereochemically isomeric forms thereof, acid or base addition salts thereof, N-oxides thereof, or quaternary ammonium derivatives thereof, wherein the dotted line is an optional bond; X is a direct b...
08/27/2002
6376534Compounds useful in pain management
Compounds of general formula I ##STR1## are disclosed and claimed in the present application, as well as their pharmaceutically acceptable salts, pharmaceutical compositions comprising the novel compounds and their use in therapy, in particular in the ...
04/23/2002
6350892Trifluoromethyl ketone analogs as selective cPLA2 inhibitors
Selective inhibitors of the cPLA2 enzymes are provided which are of use in controlling a wide variety of inflammatory diseases. The inhibitors of the present invention have the general formula ##STR1## where (R'), p, D, Y, Z, Ra, R
02/26/2002
6331564Use of triaryl methane compounds for inhibiting unwanted cellular proliferation associated with inflammatory disease
The present invention provides a class of chemical compounds useful as efficacious drugs in the treatment of sickle cell disease and diseases characterized by unwanted or abnormal cell proliferation, and in particular inflammatory diseases associated with...
12/18/2001
6329399Antifungal amine derivatives and processing for producing the same
Novel amine derivatives having an excellent antimycotic effect represented by general formula (1) below and salts thereof are provided. ##STR1## [in the formula (1, R1 represents a C1-5 alkyl group which may be halogenated, R2
12/11/2001
6313132Therapeutically active diarylpropylamines; their pharmaceutically acceptable salts; a method for their preparation and method for their use
The invention relates to novel compounds of Formula (I) wherein R1, R2, R3, R4, R5, R6, R7 and Ar are as defined in claim 1, their salts with physiologically acceptable acids and, whe...
11/06/2001
6310248Process and intermediates
The invention relates to a process for the enantioselective preparation of tolterodine and analogues and salts thereof comprises the steps of: a) enantioselectively reducing the carbonyl function in a compound of formula (II): ##STR1## wherein R1
10/30/2001
6310103S(-)-tolterodine in the treatment of urinary and gastrointestinal disorders
The S-isomer of a compound represented by the following formula: ##STR1## and pharmaceutically acceptable salts thereof is disclosed as being useful for treating urinary disorders, including urinary incontinence, and gastrointestinal disorders, including ...
10/30/2001
6306912Compounds active at a novel site on receptor-operated calcium channels useful for treatment of neurological disorders and diseases
Method for identifying a compound useful for the therapeutic treatment of a neurological disease or disorder such as stroke, head trauma, spinal cord injury, epilepsy, anxiety, or neurodegenerative diseases such as Alzheimer's Disease, Huntington's Diseas...
10/23/2001
6258842Method for the preparation of citalopram
A method for the preparation of citalopram is described comprising reaction of a compound of Formula (IV) wherein R1 is H or C1-6 alkylcarbonyl successively with a Grignard reagent of 4-halogen-fluorophenyl and a Grignard reagent of ...
07/10/2001
6191165Pharmaceutical for treatment of neurological and neuropsychiatric disorders
The invention provides a pharmaceutical for treatment of neurological and neuropsychiatric disorders comprising a compound of the formula: ##STR1## or a pharmaceutically acceptable salt thereof....
02/20/2001
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