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31. 发明授权

US07897770B2 Fluorinated dihydrotetrabenazine ether imaging agents and probes 有权
标题翻译：氟化二氢丁苯那腈成像剂和探针
公开(公告)号：US07897770B2
公开(公告)日：2011-03-01
申请号：US11923926
申请日：2007-10-25
申请人： Kande Kankanamalage Dayarathna Amarasinghe , Michael James Rishel , Sean Richard Dinn , Bruce Fletcher Johnson
发明人： Kande Kankanamalage Dayarathna Amarasinghe , Michael James Rishel , Sean Richard Dinn , Bruce Fletcher Johnson
IPC分类号： C07D455/06
CPC分类号： C07D455/06 , A61K51/0455
摘要： The present invention provides novel fluorinated ether compounds having structure I wherein R1 is a C2-C10 fluorinated aliphatic radical; R2 is a C1-C10 aliphatic radical, or a C3-C10 cycloaliphatic radical; R3 is hydrogen or a C1-C10 aliphatic radical; and R4 is hydrogen or a C1-C10 aliphatic radical. The fluorinated ether compounds are provided in both racemic and enantiomerically enriched forms and may comprise either or both of fluorine-18 and fluorine 19. The fluorinated ether compounds are shown to possess high affinity for VMAT-2, a biomarker implicated in human diabetes. The fluorinated ether compounds comprising a fluorine-18 group are useful as PET imaging agents targeting the VMAT-2 biomarker. The non-radiolabeled fluorinated ether compounds are useful as probes for the discovery of PET imaging agents.
摘要翻译：本发明提供具有结构I的新型氟化醚化合物，其中R 1是C 2 -C 10氟化脂族基; R2是C1-C10脂族基团，或C3-C10脂环族基团; R3是氢或C1-C10脂族基; 并且R 4是氢或C 1 -C 10脂族基。氟化醚化合物以外消旋和对映异构体富集的形式提供，并且可以包含氟-18和氟19中的任一种或两者。显示氟化醚化合物对于涉及人类糖尿病的生物标志物VMAT-2具有高亲和力。包含氟-18基团的氟化醚化合物可用作靶向VMAT-2生物标志物的PET显像剂。非放射性标记的氟化醚化合物可用作发现PET成像剂的探针。

32. 发明授权

US07897769B2 Intermediates for fluorinated dihydrotetrabenazine ether imaging agents and probes 有权
标题翻译：氟化二氢丁苯那嗪醚显像剂和探针的中间体
公开(公告)号：US07897769B2
公开(公告)日：2011-03-01
申请号：US11923805
申请日：2007-10-25
申请人： Kande Kankanamalage Dayarathna Amarasinghe , Michael James Rishel , Sean Richard Dinn , Bruce Fletcher Johnson
发明人： Kande Kankanamalage Dayarathna Amarasinghe , Michael James Rishel , Sean Richard Dinn , Bruce Fletcher Johnson
IPC分类号： C07D455/06
CPC分类号： C07D455/06
摘要： The present invention provides novel fluorophilic compounds having structure VI wherein R1 is a C2-C20 aliphatic, a C3-C20 cycloaliphatic, or a C3-C20 aromatic radical comprising at least one functional group susceptible to reaction with nucleophilic fluoride ion or an electrophilic fluorinating agent; R2 is a C1-C10 aliphatic radical, or a C3-C10 cycloaliphatic radical; R3 is hydrogen or a C1-C10 aliphatic radical; and R4 is hydrogen or a C1-C10 aliphatic radical. The fluorophilic compounds are provided in both racemic and enantiomerically enriched forms and are useful as intermediates in the preparation of novel PET imaging agents and probes useful in the discovery and performance assessment of PET imaging agents. The fluorophilic compounds are particularly useful in the preparation of PET imaging agents and probes having a high affinity for VMAT-2, a biomarker implicated in human diabetes and other illnesses such as Parkinson's disease.
摘要翻译：本发明提供了具有结构VI的新型氟化合物，其中R 1是C 2 -C 20脂族，C 3 -C 20脂环族或C 3 -C 20芳族基，其包含至少一个易于与亲核氟离子反应的官能团或亲电氟化剂 ; R2是C1-C10脂族基团，或C3-C10脂环族基团; R3是氢或C1-C10脂族基; 并且R 4是氢或C 1 -C 10脂族基。亲氟化合物以外消旋和对映体富集的形式提供，并且可用作制备用于PET成像剂的发现和性能评估的新型PET成像剂和探针的中间体。亲氟化合物特别可用于制备对VMAT-2具有高亲和力的PET成像剂和探针，所述VMAT-2是涉及人类糖尿病和其它疾病如帕金森病的生物标志物。

33. 发明申请

US20080306267A1 METHOD FOR MAKING TETRABENAZINE COMPOUNDS 失效
标题翻译：制备四羧酸化合物的方法
公开(公告)号：US20080306267A1
公开(公告)日：2008-12-11
申请号：US11760359
申请日：2007-06-08
申请人： Michael James Rishel , Kande Kankananamalage Dayarathna Amarasinghe , Sean Richard Dinn , Bruce Fletcher Johnson
发明人： Michael James Rishel , Kande Kankananamalage Dayarathna Amarasinghe , Sean Richard Dinn , Bruce Fletcher Johnson
IPC分类号： C07D455/06
CPC分类号： C07D455/06 , C07D217/16 , C07D217/18 , Y02P20/55
摘要： A method of preparing a tetrabenazine compound (TBZ compound) having structure I comprising the steps of reacting a nucleophilic alkenyl species with aldehyde compound II and oxidizing the resultant allylic alcohol to provide enone III. The protecting group P1 on the tetrahydroisoquinoline nitrogen is removed and the resultant deprotected intermediate is induced to undergo an amino cyclization reaction to provide a product TBZ compound having structure I. The method may be used to prepare either enantiomeric form of tetrabenazine; (+)-tetrabenazine or (−)-tetrabenazine. Alternatively the method may be adapted to provide a mixture enriched in one tetrabenazine enantiomer, a racemic mixture, or a diastereomeric mixture of tetrabenazine compounds. In addition, the present invention provides novel synthetic intermediate compositions which may be used to prepare either or both enantiomers of tetrabenazine, derivatives of tetrabenazine, and analogs of tetrabenazine.
摘要翻译：制备具有结构I的丁苯那嗪化合物（TBZ化合物）的方法包括以下步骤：使亲核烯基物质与醛化合物II反应并氧化得到的烯丙基醇以提供烯酮III。除去四氢异喹啉氮上的保护基P1，将所得脱保护的中间体诱导进行氨基环化反应，得到具有结构I的产物TBZ化合物。该方法可用于制备对映体形式的丁苯那嗪; （+） - 丁苯那嗪或（ - ） - 丁苯那嗪。或者，该方法可以适于提供富集一种四苯并嗪对映异构体，外消旋混合物或丁苯那嗪化合物的非对映体混合物的混合物。此外，本发明提供新的合成中间体组合物，其可用于制备丁苯那嗪，丁苯那敏的衍生物和丁苯那嗪的类似物之一或两者的对映异构体。

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