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filingDate 1990-11-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ae8c7f9821c5322ad75158117200a88c
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8cb83d587abbc3f36e192d6f78aee926
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_18f581a499cfc3b78310496ce95992ae
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8738c61df6b07f77d92ebb909f7409af
publicationDate 1991-09-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber HU-T56543-A
titleOfInvention Process for producing aromatic amines and pharmaceutical compositions comprising such compounds
abstract - m est un nombre entier de 1 à 3 ; - Ar et Ar représentent, indépendamment, un groupe thiényle, un groupe phényle substitué ou non substitué; un groupe imidazolyle; Ar pouvant également être un groupe benzothiényle non substitué ou substitué par un halogène; un groupe naphtyle non substitué ou substitué par un halogène; un groupe biphényle; un indolyle non substitué ou substitué; - X représente l'hydrogène; - X représente l'hydrogène, un groupe hydroxyle, ou est réuni à X ci-dessous pour former une liaison carbone-carbone; . ou bien X et X, ensemble, forment un groupe oxo ou dialkylaminoalkyloxyimino de formule = N-O-(CH 2 )p-Am, où p est 2 ou 3 et Am est un groupe dialkylamino; - Y représente un atome d'azote ou un groupe C(X") où X" est l'hydrogène ou, avec X', forme une liaison carbone-carbone; - Q représente l'hydrogène, un groupe alkyle en C 1 -C 4 ou un groupe aminoalkyle de formule -(CH 2 ) q -Am', où q est 2 ou 3 et Am est un groupe pipéridino, benzyl-4 pipéridino ou dialkylamino; - R représente l'hydrogène, un groupe méthyle ou un groupe (CH 2 ) n -L, où n est un nombre entier de 2 à 6 et L est l'hydrogène ou un groupe amino, - T représente un groupe choisi parmin W étant un atome d'oxygène ou de soufre, et - Z représente soit l'hydrogène, soit M ou OM lorsque T représente le groupen soit M lorsque T représente le groupen M représente l'hydrogène ou un alkyle droit ou ramifié; un phénylalkyle non substitué ou substitué; un pyridylalkyle; un naphtylalkyle; un pyridylthioalkyle; un styryle; un (méthyl-1) imidazolyl-2 thioalkyle ; un oxo-1 phénylindan-3 yle-2; un groupe aromatique ou hétéroaromatique non substitué ou substitué; ou un de leurs sels avec des acides minéraux ou organiques. The invention relates to compounds of formula in which : m is an integer of 1 to 3; Ar and Ar represent, independently, a thienyl group, a substituted or unsubstituted phenyl group; an imidazolyl group; Ar may also be a benzothienyl group unsubstituted or substituted by halogen; an unsubstituted or halogen substituted naphthyl group; a biphenyl group; unsubstituted or substituted indolyl; X represents hydrogen; X represents hydrogen, a hydroxyl group, or is joined at X below to form a carbon-carbon bond; . or X and X, together, form an oxo or dialkylaminoalkyloxyimino group of formula = NO- (CH 2 ) p-Am, where p is 2 or 3 and Am is a dialkylamino group; Y represents a nitrogen atom or a group C (X ") in which X" is hydrogen or, with X ', forms a carbon-carbon bond; Q represents hydrogen, a C 1 -C 4 alkyl group or an aminoalkyl group of formula - (CH 2 ) q -Am ', where q is 2 or 3 and Am is a piperidino, 4-benzylpiperidino or dialkylamino; - R represents hydrogen, a methyl group or a (CH 2 ) n -L group, where n is an integer from 2 to 6 and L is hydrogen or an amino group, T represents a group chosen from W being an oxygen or sulfur atom, and Z represents either hydrogen or M or OM when T represents the group let M be when T is the group M represents hydrogen or straight or branched alkyl; unsubstituted or substituted phenylalkyl; pyridylalkyl; a naphthylalkyl; pyridylthioalkyl; a styryle; (1-methyl-2-imidazolylthioalkyl; an oxo-1-phenylindan-3-yl-2; an unsubstituted or substituted aromatic or heteroaromatic group; or a salt thereof with inorganic or organic acids. n n n Application: neurokinin receptor antagonists.
priorityDate 1989-11-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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Total number of triples: 330.