Aromatic amine compounds, their method of preparation and...

C - Chemistry – Metallurgy – 07 – D

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C07D 211/34 (2006.01) A61K 31/445 (2006.01) A61K 31/495 (2006.01) C07D 211/14 (2006.01) C07D 211/16 (2006.01) C07D 211/18 (2006.01) C07D 211/22 (2006.01) C07D 211/28 (2006.01) C07D 211/32 (2006.01) C07D 211/70 (2006.01) C07D 295/13 (2006.01) C07D 295/15 (2006.01) C07D 295/192 (2006.01) C07D 317/58 (2006.01) C07D 317/60 (2006.01) C07D 401/06 (2006.01) C07D 401/12 (2006.01) C07D 405/12 (2006.01) C07D 409/06 (2006.01) C07D 409/12 (2006.01) C07D 413/12 (2006.01) C07D 417/12 (2006.01) C07D 521/00 (2006.01)

Patent

CA 2029275

IN THE UNITED STATES PATENT AND TRADEMARK OFFICE PATENT APPLICATION entitled: Aromatic amine compounds, their method of preparation and pharmaceutical compositions in which they are present in the names of: Xavier EMONDS-ALT Pierre GOULAOUIC Vincenzo PROIETTO Didier VAN BROECK Assignee: SANOFI ABSTRACT OF THE DISCLOSURE The invention relates to compounds of the formula Image (I) in which: - m is an integer from 1 to 3; - Ar and Ar' independently are a thienyl group; a substituted or unsubstituted phenyl group; or an imidazolyl group; it also being possible for Ar- to be a benzothienyl group which is unsubstituted or substituted by a halogen; a naphthyl group which is unsubstituted or substituted by a halogen; a biphenyl group; or a substituted or unsubstituted indolyl; - X is hydrogen; - X' is hydrogen or a hydroxyl group or is joined to X" below to form a carbon-carbon bond, ? or X and X' together form an oxo group or a di- alkylaminoalkoxyimino group of the formula =N-O-(CHz)p-Am, in which p is 2 or 3 and Am is a dialkylamino group; - Y is a nitrogen atom or a group C(X"), in which X" is hydrogen or forms a carbon-carbon bond with X'; - Q is hydrogen, a C1-C4 alkyl group or an aminoalkyl group of the formula -(CH2)q-Am', in which q is 2 or 3 and Am' is a piperidino, 4-benzylpiperidino or dialkylamino group; R is hydrogen, a methyl group or a group (CH2)n-L, in which n is an integer from 2 to 6 and L is hydrogen or an amino group; _ T is a group selected from Image and Image W being an oxygen or sulfur atom; and - Z is either hydrogen, or M or OM when T is the group -C(=O)-, or M when T is the group -C(=W)-NH-, M being hydrogen; a linear or branched alkyl; a substituted or unsubstituted phenylalkyl; a pyridylalkyl; a naphthylalkyl; a pyridylthioalkyl; a styryl; a 1- methylimidazol-2-ylthioalkyl; a 1-oxophenyl-3-indan- 2-yl; or a substituted or unsubstituted aromatic or heteroaromatic group; or to one of their salts with mineral or organic acids. Application: neurokinin receptor antagonists.

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