- 专利标题: Propanamine derivatives as serotonin and norepinephrine reuptake inhibitors
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申请号: US10532765申请日: 2003-10-24
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公开(公告)号: US07410982B2公开(公告)日: 2008-08-12
- 发明人: Serge Louis Boulet , Sandra Ann Filla , Peter Thaddeus Gallagher , Kevin John Hudziak , Anette Margareta Johansson , Rushad E. Karanjawala , John Joseph Masters , Brian Michael Mathes , Richard Edmund Rathmell , Maria Ann (nee Fagan) Whatton , Victor Matassa , Chad Nolan Wolfe
- 申请人: Serge Louis Boulet , Sandra Ann Filla , Peter Thaddeus Gallagher , Kevin John Hudziak , Anette Margareta Johansson , Rushad E. Karanjawala , John Joseph Masters , Brian Michael Mathes , Richard Edmund Rathmell , Maria Ann (nee Fagan) Whatton , Victor Matassa , Chad Nolan Wolfe
- 申请人地址: US IN Indianapolis
- 专利权人: Eli Lilly and Company
- 当前专利权人: Eli Lilly and Company
- 当前专利权人地址: US IN Indianapolis
- 代理商 Robert D. Titus; Arvie J. Anderson
- 国际申请: PCT/US03/31512 WO 20031024
- 国际公布: WO2004/043931 WO 20040527
- 主分类号: A61K31/4365
- IPC分类号: A61K31/4365 ; C07D409/02
摘要:
There is provided a heretoaryloxy/thio 3-substituted propanamine compound of formula (I) wherein A is selected from —O— and —S—; X is selected from phenyl optionally substituted with up to 5 substituents each independently selected from halo, C1-C4 alkyl and C1-C4 alkoxy, thienyl optionally substituted with up to 3 substituents each independently selected from halo and C1-C4 alkyl, and C2-C8 alkyl, C2-C8 alkenyl, C3-C8 cycloalkyl and C4-C8 cycloalkylalkyl, each of which may be optionally substituted with up to 3 substituents each independently selected from halo, C1-C4 alkyl, C1-C4 alkoxy, C1-C4 alkyl —S(O)n— where n is 0, 1 or 2, —CF3, —CN and —CONH2; Y is selected from dihydrobenzothienyl, benzothiazolyl, benzoisothiazolyl, quinolyl, isoquinolyl, naphthyridyl, and thienopyridyl, each of which may be optionally substituted with up to 4 or, where possible, up to 5 substituents each independently selected from halo, C1-C4 alkyl, C1-C4 alkoxy, C1-C4 alkyl-S(O)n— where n is 0, 1 or 2, nitro acetyl, —CF3, —SCF3 and cyano; Z is selected from H, OR3 or F, wherein R3 is selected from H, C1-C6 alkyl and phenyl C1C6 alkyl; R1 and R2 are each independently H or C1-C4 alkyl; and pharmaceutically acceptable salts thereof.
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