[EN] BICYCLIC HETEROAROMATIC COMPOUNDS USEFUL AS LH AGONISTS<br/>[FR] COMPOSES HETEROAROMATIQUES BICYCLIQUES UTILES EN TANT QU'AGONISTES DE L'HORMONE LUTEINISANTE (LH)
申请人:AKZO NOBEL NV
公开号:WO2000061586A1
公开(公告)日:2000-10-19
The invention relates to a bicyclic heteroaromatic derivative compound according to general formula (I), or a pharmaceutically acceptable salt thereof, wherein R?1 is NR5R6, OR5, SR5 or R7; R5 and R6¿ are independently selected from H, (1-8C)alkyl, (2-8C)alkenyl, (2-8C)alkynyl, (3-8C)cycloalkyl, (2-7C)heterocycloalkyl, alkyl(1-8C)carbonyl, (6-14C)arylcarbonyl, (6-14C)aryl or (4-13C)heteroaryl, or R?5 and R6¿ together are joined in a (2-7C)heterocycloalkyl ring; R7 is (3-8C)cycloalkyl, (2-7C)heterocycloalkyl, (6-14C)aryl or (4-13C)heteroaryl, R2 is (1-8C)alkyl, (2-8C)alkenyl, (2-8C)alkynyl, or (6-14C)aryl or (4-13C)heteroaryl, both optionally substituted with one or more substituents selected from (1-8C)alkyl, (1-8C)alkylthio, (1-8C)(di)alkylamino, (1-8C)alkoxy, (2-8C)alkenyl, or (2-8C)alkynyl; R3 is (1-8C)alkyl, (2-8C)alkenyl, (2-8C)alkynyl, (3-8C)cycloalkyl, (2-7C)heterocycloalkyl, or (6-14C)aryl or (4-13C)heteroaryl, both optionally substituted with one or more substituents selected from (1-8C)alkyl, (1-8C)(di)alkylamino or (1-8C)alkoxy; X is S, O or N(R4); R4 is H, (1-8C)alkyl, (1-8C)alkylcarbonyl, (6-14C)arylcarbonyl or (6-14C)aryl(1-8C)alkyl; Y is CH or N; Z is NH¿2? or OH; A is S, N(H), N(R?9¿), O or a bond; R9 can be selected from the same groups as described for R2 and B is N(H), O or a bond. The compounds of the invention have LH receptor activating activity and can be used in fertility regulating therapies.
本发明涉及一种具有一般式(I)的双环杂芳基衍生物化合物或其药学上可接受的盐,其中R1为NR5R6,OR5,SR5或R7;R5和R6分别选自H、(1-8C)烷基、(2-8C)烯基、(2-8C)炔基、(3-8C)环烷基、(2-7C)杂环烷基、烷基(1-8C)羰基、(6-14C)芳基羰基、(6-14C)芳基或(4-13C)杂芳基,或R5和R6在(2-7C)杂环烷基环中连接;R7为(3-8C)环烷基、(2-7C)杂环烷基、(6-14C)芳基或(4-13C)杂芳基,R2为(1-8C)烷基、(2-8C)烯基、(2-8C)炔基、或(6-14C)芳基或(4-13C)杂芳基,均可选择地取代一个或多个取代基,所述取代基选自(1-8C)烷基、(1-8C)烷基硫、(1-8C)(二)烷基胺基、(1-8C)烷氧基、(2-8C)烯基或(2-8C)炔基;R3为(1-8C)烷基、(2-8C)烯基、(2-8C)炔基、(3-8C)环烷基、(2-7C)杂环烷基、或(6-14C)芳基或(4-13C)杂芳基,均可选择地取代一个或多个取代基,所述取代基选自(1-8C)烷基、(1-8C)(二)烷基胺基或(1-8C)烷氧基;X为S、O或N(R4);R4为H、(1-8C)烷基、(1-8C)烷基羰基、(6-14C)芳基羰基或(6-14C)芳基(1-8C)烷基;Y为CH或N;Z为NH2或OH;A为S、N(H)、N(R9)、O或键;R9可以选择与R2相同的基团;B为N(H)、O或键。本发明的化合物具有LH受体激活活性,可用于调节生育的治疗中。