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Class 549/492 - Nitrogen and the hetero ring are single bonded directly to the same acyclic saturated hydrocarbon group


Subclass of Class 549 - Organic compounds -- part of the class 532-570 series
Definition: Compounds wherein nitrogen and the hetero ring are single
No. of patents: 115
Last issue date: 08/19/2008


1      
NumberTitleIssue Date
7414073Cytotoxic agents containing novel potent taxanes and their therapeutic use
Included within the scope of the present invention are potent taxanes and taxanes containing a linking group. Also included is a cytotoxic agent comprising one or more taxanes linked to a cell binding agent. A therapeutic composition for inducing cell death in selec...
08/19/2008
7396858Biguanide derivative and therapeutic agent for diabetes containing the same
Diabetes treatments comprising, as effective ingredients, biguanide derivatives represented by the following general formula (1), or salts thereof. (wherein R1, R2 and R3 may be the same or ...
07/08/2008
7122571Substituted hydrazones as inhibitors of cyclooxygenase-2
Compounds useful as inhibitors of cyclooxygenase-2 activity have the formulae I or Ia: wherein: Q1, Q2, n, m, X, Y and R are as defined herein.
10/17/2006
7030239Compounds to treat Alzheimer's disease
The present invention is directed toward substituted hydroxyethylene compounds of formula (XII) useful in treating Alzheimer's disease and other similar diseases. ...
04/18/2006
6946565Process for the preparation of an indole derivative
A process for the preparation of methyl 2-(3-chloropropoxy)-indole-3-carboxylate, which comprises reacting a 3-chloro-3-carboxylate indole compound with 3-chloropropanol in the presence of an acid having a pKa of from 0 to 2. ...
09/20/2005
6852750Benzenedicarboxylic acid derivatives
New benzenedicarboxylic acid derivative compounds; pharmaceutical compositions, diagnostic methods, and diagnostic kits that include those compounds; and methods of using those compounds for inhibiting NAALADase enzyme activity, detecting diseases where NAALADase le...
02/08/2005
6849634Potassium channel inhibitors
Compounds useful as potassium channel inhibitors and especially useful for the treatment of cardiac arrhythmias and cell proliferative disorders are described. ...
02/01/2005
6780998Substituted 2-aminoalkyl-1,4-diaminobenzene compounds and oxidation dye precursor compositions containing same
The oxidation hair dye precursor composition contains from 0.005 to 20.0 percent by weight of one or more coupler compounds and from 0.005 to 20.0 percent by weight of one or more developer compounds. The one or more developer compounds include at least one substitu...
08/24/2004
6677330Fluorides of 4-substituted piperidine derivatives
The present invention provides a novel compound having an excellent acetylcholinesterase inhibitory effect. That is, it provides a 4-substituted piperidine compound fluoride represented by the following formula, a pharmaceutically acceptable salt thereof ...
01/13/2004
6579993Process for the preparation of 1-(3-dimethylaminopropyl)-1-(4-fluorophenyl)-1,3-dihydroisobenzofuran-5-ca rbonitrile
Method for the preparation of 1-(3-dimethylaminopropyl)-1-(4-fluoro-phenyl)-1,3-dihydroisobenzofuran-5-c arbonitrile (citalopram) comprising the reaction of a compound of formula ##STR1## wherein X is a halogen, with organometallic dimethylaminopropyl hali...
06/17/2003
6369059Tetracyclic derivatives, process of preparation and use
A compound of formula (I) ##STR1## and salts and solvates thereof, in which: R0 represents hydrogen, halogen or C1-6 alkyl; R1 represents hydrogen, C1-6 alkyl, C2-6 alkenyl, C2-6 alkynyl, haloC
04/09/2002
6358883Pesticidal and parasiticidal use of 1-aryl-1-(substituted thio, sulfinyl and sulfonyl)-2-nitroethane compounds
The present invention relates to the pesticidal use of 1-aryl-1-(substituted thio, sulfinyl and sulfonyl)-2-nitroethane compounds having the structural formula I ##STR1##...
03/19/2002
6329523Compounds having a plurality of nitrogenous substitutents
Novel compounds having the formula: ##STR1## wherein the constituent variables are defined herein. The compounds are constructed to include a central aromatic, aliphatic, or heterocyclic ring system. Attached to the central ring system are two linear grou...
12/11/2001
6281365(Gem-heterocyclodimethanamine-n,n')platinum complexes
Organic platinum complexes active as anti-tumor agents in warm-blooded animals, and methods for synthesis of same, are described....
08/28/2001
6255340Pesticidal composition
A pesticidal composition comprising prallethrin and a neonicotinoid compound given in the following formula (1), (2) or (3), as an active ingredient ##STR1## wherein, A represents a 6-chloro-3-pyridyl, 2-chloro-5-thiazolyl, tetrahydrofuran-2-yl, tetr...
07/03/2001
6252072Method for producing nitroguanidine derivatives
A process for the preparation of compounds of formula ##STR1## is described, wherein R1 is hydrogen or C1 -C4 -alkyl; R2 is hydrogen, C1 -C6 -alkyl, C3 -C6 -cycloalkyl or a...
06/26/2001
6200353Coupler for use in oxidative hair dyeing
Couplers for hair coloring compositions for oxidative dyeing of hair are compounds of the formula at least one coupler comprising a compound of the formula: ##STR1## wherein R is selected from the group consisting of C1 to C2 alkyl ...
03/13/2001
6077954Substituted heterocyclic compounds
Novel compounds having the formula: ##STR1## wherein the constituent variables are defined herein. The compounds are constructed to include a central aromatic, aliphatic, or heterocyclic ring system. Attached to the central ring system are two linear...
06/20/2000
6048882Prophylactic and therapeutic agent for hepatic diseases
Hepatic diseases can be prevented or treated by administering an isoprenylamine derivative represented by the general formula (II) ##STR1## [wherein n represents an integer of 4-12, m represents an integer of 0-3, Ar represents a phenyl group, a fury...
04/11/2000
5856323Compounds and methods for the treatment of disorders mediated by platelet activating factor or products of 5-lipoxygenase
2,5-Diaryl tetrahydrofurans, 2,5-diaryl tetrahydrothiophenes, 2,4-diaryl tetrahydrofurans, 2,4-diaryl tetrahydrothiophenes, 1,3-diaryl cyclopentanes, 2,4-diaryl pyrrolidines, and 2,5-diaryl pyrrolidines are disclosed that reduce the chemotaxis and respira...
01/05/1999
5843972Heterocyclic ଲ-adrenergic agonists
The present invention relates to certain compounds of the formula (I) the racemic-enantiomeric mixtures and optical isomers of said compounds and the pharmaceutically acceptable salts or prodrugs thereof, depicted below, which are ଲ-adrenergic recep...
12/01/1998
5807886Bicyclic amidine dervatives as inhibitors of nitric oxide synthetase
Compounds of the formula (I) ##STR1## wherein D represents a 5-membered heterocyclic aromatic ring containing 1 to 4 heteroatoms selected from O, N or S, optionally substituted at a carbon atom by halogen, trifluoromethyl, alkyl C1 to 6, nitro, cyano...
09/15/1998
5672724Processes for preparing ranitidine
The present invention relates to a novel method for preparing ranitidine and pharmaceutically acceptable salts thereof....
09/30/1997
5663381Process for preparing form 1 ranitidine hydrochloride
A process for preparing pure N-[2-[[[5-[dimethylamino)-methyl-2-furanyl]methyl]thio]ethyl]-N'-methyl-2- nitro-1,1-ethyldiamine hydrochloride, designated Form 1 ranitidine hydrochloride, from ranitidine in methylene chloride with the addition of hydroc...
09/02/1997
5621120Process for the manufacture of form 1 ranitidine hydrochloride
A process for the manufacture of Form 1 ranitidine hydrochloride (N-[2-[[[5-(Dimethylamino)methyl]-2-furanyl]methyl]thio]ethyl-N'-methyl-2- nitro-1,1-ethenediamine) hydrochloride, is described. A process to convert ranitidine hydrochloride Form 2 to Form 1...
04/15/1997
5618980Method for preparing aromatic secondary amino compound
Disclosed are (1) a method for preparing an aromatic secondary amino compound which comprises reacting an N-cyclohexylideneamino compound in the presence of a hydrogen moving catalyst and a hydrogen acceptor by the use of a sulfur-free polar solvent and/o...
04/08/1997
5536878Method for preparing aromatic secondary amino compound
Disclosed are (1) a method for preparing an aromatic secondary amino compound which comprises reacting an N-cyclohexylideneamino compound in the presence of a hydrogen moving catalyst and a hydrogen acceptor by the use of a sulfur-free polar solvent and/o...
07/16/1996
5532267Amidinonaphthyl furancarboxylate derivatives and acid addition salts therof
Amidinonaphthyl furancarboxylate derivatives of the formula I ##STR1## wherein A is a single bond or A denotes (a) a phenyl group, cyclopentyl group, or cyclohexyl group, (b) an alkenylphenyl group, alkylphenyl group, phenylalkenyl group, or phenylal...
07/02/1996
5462963Chelator compositions comprising ଱-diamine compounds
The present invention involves photoprotective compositions which are useful for topical application to prevent damage to skin caused by acute or chronic exposure to ultraviolet light comprising chelating agents having the structure: ##STR1## wh...
10/31/1995
5434151Compounds and methods for the treatment of disorders mediated by platelet activating factor or products of 5-lipoxygenase
2,5-Diaryl tetrahydrofurans, 2,5-diaryl tetrahydrothiophenes, 2,4-diaryl tetrahydrofurans, 2,4-diaryl tetrahydrothiophenes, 1,3-diaryl cyclopentanes, 2,4-diaryl pyrrolidines, and 2,5-diaryl pyrrolidines are disclosed that reduce the chemotaxis and respira...
07/18/1995
5434181Furanyl insecticide
The present invention relates to novel (tetrahydro-3-furanyl)methylamino derivatives of the following formula (1): ##STR1## wherein the variables are defined in the specification, which are useful as insecticides....
07/18/1995
5391772Converting an alcohol to an azide with SN 2 inversion using a phosphoryl azide
Described is a process for converting an alcohol to an azide with SN 2 inversion using a phosphoryl azide, e.g. diphenylphosphoryl azide (DPPA). Good yields of azide in high enantiomeric excess can be achieved specifically for benzylic alcohols...
02/21/1995
5358938Compounds and methods for the treatment of disorders mediated by platelet activating factor or products of 5-lipoxygenase
2,5-Diaryl tetrahydrofurans, 2,5-diaryl terahydrothiophenes, 2,4-diaryl tetrahydrofurans, 2,4-diaryl tetrahydrothiphenes, 1,3-diaryl cyclopentanes, 2,4-diaryl pyrrolidines, and 2,5-diaryl pyrrolidines are disclosed that reduce the chemotaxis and respirato...
10/25/1994
5338871Preparation of form 1 ranitidine hydrochloride
Pure Form 1 ranitidine hydrochloride is prepared by a process of crystallization from a solution of ranitidine hydrochloride in a mixed solvent comprising 1 part by volume of at least one lower alkanol such as ethanol and 1-2.0 parts by volume of a C...
08/16/1994
52927604-heteroaryl-1,3-benzodiazepines and 2-substituted-଱-(heteroaryl)benzeneethanamines
Novel 4,5-dihydro-4-heteroaryl-3H-1,3-benzodiazepines, intermediates, processes for the preparation thereof, and methods for treating depression, inhibiting convulsions and treating anxiety utilizing compounds and compositions thereof are disclosed....
03/08/1994
5284853Angiotensin II receptor blocking 2,3,6 substituted quinazolinones
The invention provides novel 2, 3, 6 substituted quinazolinones of the formula ##STR1## wherein, R, R6 and X are defined in the specification which have activity as angiotensin II (AII) antagonists....
02/08/1994
5229418Carboxylic acid derivatives
The invention relates to a salt of a basic histamine H2 -receptor antagonist of formula (I) ##STR1## and a complex of bismuth with a carboxylic acid selected from tartaric acid, citric acid and alkyl citric acids, or a solvate of such a sa...
07/20/1993
5227401Ethynyl alanine amino diol compounds for treatment of hypertension
Compounds characterized generally as ethynyl alanine amino diol derivatives are useful as renin inhibitors for the treatment of hypertension. Compounds of particular interest are those of Formula I ##STR1## wherein A is selected from CO and SO2
07/13/1993
5223535Propargyl glycine amino propargyl diol compounds for treatment of hypertension
Compounds characterized generally as propargyl glycine amino propargyl diol derivatives are useful as renin inhibitors for the treatment of hypertension. Compounds of particular interest are those of Formula I ##STR1## wherein A is selected from CO a...
06/29/1993
5217991Cycloalkyl/cycloalkylalkyl-N-terminal cycloalkoxy-C-terminal amino hydroxy ଲ-amino acid derivatives
Non-peptidyl compounds characterized generally as cycloalkyl/cycloalkylalkyl-N-terminal cycloalkoxy-C-terminal amino hydroxy ଲ-amino acid derivatives are useful as renin inhibitors for treatment of hypertension. Compounds of particular interest are ...
06/08/1993
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