发明名称 ANTIBACTERIAL TYLOSIN DERIVATIVES AND METHODS FOR THEIR PREPARATION
摘要 The present invention relates to new macrolide derivatives, in particular new tylosin derivatives of the formula (I); a pharmaceutical or veterinary composition comprising the derivatives; a method for preparation thereof; a method for treating and/or preventing bacterial infections in an animal, wherein the method comprises administering the derivatives or the composition; and a use of the derivatives for the manufacture of medicaments for treating and/or preventing bacterial infections in an animal.;
申请公布号 US2014349954(A1) 申请公布日期 2014.11.27
申请号 US201214360713 申请日期 2012.11.21
申请人 Bayer Intellectual Property GmbH ;The Kitasako Institute 发明人 Kleefeld Gerd;Froyman Robrecht;Dörner Julia Charlotte;Ludwig Carolin;Omura Satoshi;Toshiaki Sunazuka;Tomoyasu Hirose;Akihiro Sugawara;Kazuro Shiomi
分类号 C07H17/08;C07H1/00 主分类号 C07H17/08
代理机构 代理人
主权项 1. A compound represented by the formula (I): or a pharmaceutically acceptable salt, ester, prodrug or solvate thereof; wherein, A is selected from the group consisting of: (1) —CHO or a protected aldehyde; (2) CH2—X, wherein X is selected from the group consisting of: a. hydroxy or protected hydroxy; b. halogen; and c. —N3 (3) —CN; (4) —CH═N—NR7R8, wherein R7 and R8 are each independently selected from hydrogen, C1-C6-alkyl, optionally substituted with one or more substituents selected from the group consisting of halogen, aryl, substituted aryl, heterocyclic and substituted heterocyclic, C2-C6-alkenyl, optionally substituted with one or more substituents selected from the group consisting of halogen, aryl, substituted aryl, heterocyclic and substituted heterocyclic, C2-C6-alkynyl, optionally substituted with one or more substituents selected from the group consisting of halogen, aryl, substituted aryl, heterocyclic and substituted heterocyclic or R7 and R8 taken with the nitrogen atom to which they are connected form a 3- to 7-membered ring which may optionally contain a hetero function selected from the group consisting of —O—, —NH—, —N(C1-C6-alkyl)-, —N(aryl)-N (heteroaryl)-, —S—, —S(O)— and —S(O)2—; (5) —CH═N—OR7, wherein R7 is as previously defined; (6) C3-C14-cycloalkyl; (7) substituted C3-C14-cycloalkyl; (8) aryl; (9) substituted aryl; (10) heterocyclic; (11) substituted heterocyclic; and (12) CH2—R; R1 and R2 are each independently selected from the group consisting of: (1) hydrogen; (2) hydroxy; (3) protected hydroxy; (4) —OC(O)—C1-C12-alkyl, optionally substituted with one or more substituents selected from the group consisting of halogen, aryl, substituted aryl, heterocyclic, substituted heterocyclic, —O—R7 and —NR7R8 where R7 and R8 are as previously defined; (5) —O—R7, where R7 is as previously defined; (6) halogen; (7) —NR7R8, where R7 and R8 are as previously defined; (8) R1 and R2 taken together are oxo; and (9) R1 and R2 taken together are ═N—O—C0-C3-alkyl-R; R3 is selected from the group consisting of: (1) hydrogen; (2) a hydroxy protecting group; (3) —C(O)—C1-C12-alkyl, optionally substituted with one or more substituents selected from the group consisting of halogen, aryl, substituted aryl, heterocyclic, substituted heterocyclic, —O—R7 and —NR7R8 where R7 and R8 are as previously defined; (4) C1-C6-alkyl, optionally substituted with one or more substituents selected from the group consisting of halogen, aryl, substituted aryl, heterocyclic, substituted heterocyclic, —O—R7 and —NR7R8 where R7 and R8 are as previously defined; (5) C2-C6-alkenyl, optionally substituted with one or more substituents selected from the group consisting of halogen, aryl, substituted aryl, heterocyclic, substituted heterocyclic, —O—R7 and —NR7R8 where R7 and R8 are as previously defined; and (6) C2-C6-alkynyl, optionally substituted with one or more substitutents selected from the group consisting of halogen, aryl, substituted aryl, heterocyclic, substituted heterocyclic, —O—R7 and —NR7R8 where R7 and R8 are as previously defined; R4 is -M-Y, where M is: (1) absent, (2) —C(O)—, (3) —C(O)N(R7)-, where R7 is as previously defined, (4) —C1-C6-alkyl-N(R7)-, where R7 is as previously defined, (5) —C2-C6-allcenyl-N(R7)-, where R7 is as previously defined, or (6) —C2-C6-alkynyl-N(R7)-, where R7 is as previously defined; and where Y is: (1) hydrogen, (2) hydroxy protecting group, (3) C1-C6-alkyl, optionally substituted with one or more substituents selected from the group consisting of halogen, aryl, substituted aryl, heterocyclic and substituted heterocyclic, —OR7 where R7 is as previously defined, (4) C2-C6-alkenyl, optionally substituted with one or more substituents selected from the group consisting of halogen, aryl, substituted aryl, heterocyclic and substituted hetreocyclic, —OR7 where R7 is as previously defined, (5) C2-C6-alkynyl, optionally substituted with one or more substituents selected from the group consisting of halogen, aryl, substituted aryl, heterocyclic and substituted heterocyclic, —OR7 where R7 is as previously defined, (6) aryl, (7) substituted aryl, (8) heterocyclic, or (9) substituted heterocyclic; R5 is selected from the group consisting of: (1) hydrogen; (2) hydroxy; (3) protected hydroxy; (4) halogen; (5) —O—R7, where R7 is as previously defined; (6) —N3 or R; RP is hydrogen or a hydroxy protecting group; and each R′ is independently [1,4]-epi-[1,2,3]-triazoro-R; and where each R is independently selected from the group consisting of: (1) C1-C9-alkyl, optionally substituted with one or more substituents selected from the group consisting of halogen, aryl, substituted aryl, heterocyclic and substituted heterocyclic, —OR7 where R7 is as previously defined; (2) C2-C9-alkenyl, optionally substituted with one or more substituents selected from the group consisting of halogen, aryl, substituted aryl, heterocyclic and substituted heterocyclic, —OR7 where R7 is as previously defined; (3) C2-C9-alkynyl, optionally substituted with one or more substituents selected from the group consisting of halogen, aryl, substituted aryl, heterocyclic and substituted heterocyclic, —OR7 where R7 is as previously defined; (4) C3-C14-cycloalkyl; (5) substituted C3-C14-cycloalkyl; (6) aryl; (7) substituted aryl; (8) heterocyclic; (9) substituted heterocyclic; and (10) —COOR7, where R7 is as previously defined; provided that at least one of A, R1 and R2 and R5 comprise R′.
地址 Monheim DE