发明名称 6,7-dihydro-pyrazolo[1,5-a]pyrazin-4-ylamine derivatives useful as inhibitors of beta-secretase (BACE)
摘要 The present invention relates to novel 6,7-dihydro-pyrazolo[1,5-a]pyrazin-4-yl-amine derivatives as inhibitors of beta-secretase, also known as beta-site amyloid cleaving enzyme, BACE, BACE1, Asp2, or memapsin2. The invention is also directed to pharmaceutical compositions comprising such compounds, to processes for preparing such compounds and compositions, and to the use of such compounds and compositions for the prevention and treatment of disorders in which beta-secretase is involved, such as Alzheimer's disease (AD), mild cognitive impairment, senility, dementia, dementia with Lewy bodies, Down's syndrome, dementia associated with stroke, dementia associated with Parkinson's disease or dementia associated with beta-amyloid.
申请公布号 US9346811(B2) 申请公布日期 2016.05.24
申请号 US201214002169 申请日期 2012.02.29
申请人 JANSSEN PHARMACEUTICA NV 发明人 Trabanco-Suárez Andrés Avelino;Gijsen Henricus Jacobus Maria;Van Gool Michiel Luc Maria;Vega Ramiro Juan Antonio;Delgado-Jiménez Francisca
分类号 A61K31/4985;A61K31/41;C07D487/04 主分类号 A61K31/4985
代理机构 代理人 Stercho Yuriy P.
主权项 1. A compound of Formula (I) or a tautomer or a stereoisomeric form thereof, wherein R1 and R2 are independently selected from the group consisting of hydrogen, halo, cyano, C1-3alkyl, mono- and polyhalo-C1-3alkyl or C3-6cycloalkyl; R3 is selected from the group consisting of hydrogen, C1-3alkyl, C3-6cycloalkyl, mono- and polyhalo-C1-3alkyl, homoaryl and heteroaryl; X1, X2, X3, X4 are independently C(R4) or N, provided that no more than two thereof represent N; each R4 is selected from the group consisting of hydrogen, halo, C1-3alkyl, mono- and polyhalo-C1-3alkyl, cyano, C1-3alkyloxy, mono- and polyhalo-C1-3alkyloxy; L is a bond or —N(R5)CO—, wherein R5 is hydrogen or C1-3alkyl; Ar is homoaryl or heteroaryl; wherein homoaryl is phenyl or phenyl substituted with one, two or three substituents selected from the group consisting of halo, cyano, C1-3alkyl, C1-3 alkyloxy, mono- and polyhalo-C1-3 alkyl, mono- and polyhalo-C1-3 alkyloxy; heteroaryl is selected from the group consisting of pyridyl, pyrimidyl, pyrazyl, pyridazyl, furanyl, thienyl, pyrrolyl, pyrazolyl, imidazolyl, triazolyl, thiazolyl, thiadiazolyl, oxazolyl, and oxadiazolyl, each optionally substituted with one, two or three substituents selected from the group consisting of halo, cyano, C1-3alkyl, C1-3alkyloxy, mono- and polyhalo-C1-3alkyl, mono- and polyhalo-C1-3alkyloxy; or an addition salt or a solvate thereof.
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