摘要 |
The invention relates to novel substituted naphthyridines of formula 1 as well as pharmacologically acceptable salts, diastereomers, enantiomers, racemates, hydrates, or solvates thereof. In formula 1, R1 can represent a group A selected from among the group comprising -O-R3, -NR3 R4, -CR3 R4 R5,-(ethyne)-R3, -S-R3, -SO-R3, and SO2 -R3, or R1 represents a group B selected from among the group comprising: - C6-10-aryl; - a five-membered to ten-membered, monocyclic or bicyclic heteroaryl containing 1 to 3 heteroatoms independently selected from among the group comprising N, O, and S, wherein said heteroaryl is linked to the structure according to formula 1 via a C atom or an N atom; - a three-membered to ten-membered, monocyclic or bicyclic, saturated or partially saturated heterocycle containing 1 to 3 heteroatoms independently selected from among the group comprising N, O, and S, wherein said heterocycle is linked to the structure according to formula 1 via a C atom or an N atom; and - a 5-membered to 11-membered spiro group which can optionally contain 1, 2, or 3 heteroatoms independently selected from among the group comprising N, O, and S, wherein said spiro group is linked to the structure according to formula 1 via a C atom or an N atom, wherein said group B can be optionally substituted as described in claim 1, and R3,R4,R5, R6, and m can have the meanings indicated in claim 1. The invention also relates to pharmaceutical compositions containing said compounds. |
申请人 |
BOEHRINGER INGELHEIM INTERNTIONAL GMBH;FIEGEN, DENNIS;HANDSCHUH, SANDRA;HOBBIE, SILKE;HOFFMANN, MATTHIAS;KONO, TAKESHI;SATO, YAYOI;SCHNAPP, ANDREAS;SCHULER-METZ, ANNETTE |
发明人 |
FIEGEN, DENNIS;HANDSCHUH, SANDRA;HOBBIE, SILKE;HOFFMANN, MATTHIAS;KONO, TAKESHI;SATO, YAYOI;SCHNAPP, ANDREAS;SCHULER-METZ, ANNETTE |