Pyrrolopyrimidine and pyrrolopyridine derivatives...

C - Chemistry – Metallurgy – 07 – D

Patent

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Details

C07D 487/04 (2006.01) A61K 31/4375 (2006.01) A61K 31/439 (2006.01) A61K 31/519 (2006.01) A61P 25/00 (2006.01) C07D 209/00 (2006.01) C07D 221/00 (2006.01) C07D 239/00 (2006.01) C07D 451/00 (2006.01) C07D 471/04 (2006.01) C07D 519/00 (2006.01) C07F 9/6561 (2006.01)

Patent

CA 2485556

[PROBLEM TO BE SOLVED] An object of the present invention is to provide an antagonist against CRF receptors which is effective as a therapeutic or prophylactic agent for diseases in which CRF is considered to be involved, such as depression, anxiety, Alzheimer's disease, Parkinson's disease, Huntington's chorea, eating disorder, hypertension, gastric diseases, drug dependence, epilepsy, cerebral infarction, cerebral ischemia, cerebral edema, cephalic external wound, inflammation, immunity-related diseases, alopecia, irritable bowel syndrome, sleep disorders, epilepsy, dermatitides, schizophrenia, etc. [SOLUTION] A pyrrolopyrimidine or pyrrolopyridine derivative substituted with a cyclic amino group represented by the following formula [I]: (see formula I) has a high affinity for CRF receptors and is effective against diseases in which CRF is considered to be involved.

La présente invention a pour objet de fournir un antagoniste dirigé contre les récepteurs du facteur de libération de la corticotropine (CRF), qui soit efficace en tant qu'agent thérapeutique ou prophylactique pour les maladies dans lesquelles le facteur CRF est sensé être impliqué, telles que la dépression, l'anxiété, la maladie d'Alzheimer, la maladie de Parkinson, la chorée de Huntington, les troubles de l'alimentation, l'hypertension, les maladies gastriques, la pharmacodépendance, l'épilepsie, l'infarctus cérébral, l'ischémie cérébrale, l'oedème cérébral, les blessures externes céphaliques, les inflammations, les maladies immunitaires, l'alopécie, le syndrome du colon irritable, les troubles du sommeil, l'épilepsie, les dermatites, la schizophrénie, etc. L'invention se rapporte ainsi à un dérivé de pyrrolopyrimidine ou de pyrrolopyridine à substitution par un groupe amino cyclique, représenté par la formule suivante [I], qui possède une haute affinité pour les récepteurs du CRF et s'avère efficace contre les maladies dans lesquelles le facteur CRF est supposé être impliqué.

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