US2013023525A1PendingUtilityA1
Gyrase inhibitors and uses thereof
Est. expiryJan 31, 2023(expired)· nominal 20-yr term from priority
Inventors:Paul S. CharifsonDavid DeiningerAnne-Laure GrillotYusheng LiaoSteven RonkinDean StamosEmanuele PerolaTiansheng WangArnaud Le TiranJoseph Drumm
A61P 31/06A61P 43/00A61P 31/04A61P 31/00C07D 491/04A61P 11/00C07D 405/04A61P 13/08A61P 17/00C07D 471/04C07D 417/14C07D 401/14A61P 13/02C07D 403/04C07D 413/14C07D 487/04C07D 403/14C07D 405/14
54
PatentIndex Score
0
Cited by
0
References
0
Claims
Abstract
The present invention relates to compounds which inhibit bacterial gyrase and/or Topo IV and pharmaceutically acceptable compositions comprising said compounds. These compounds, and compositions thereof, are useful in treating bacterial infection. Accordingly, the present invention also relates to methods for treating bacterial infections in mammals.
Claims
exact text as granted — not AI-modified1 . A compound of formula I:
or a pharmaceutically acceptable salt thereof, wherein:
W is selected from nitrogen, CH, or CF;
X is selected from CH or CF;
Z is O or NH;
R 1 is phenyl or a 5-6 membered heteroaryl ring having 1-3 heteroatoms independently selected from oxygen, nitrogen, or sulfur, wherein:
R 1 is substituted with 0-3 groups independently selected from -(T) y -Ar, R′, oxo, C(O)R′, CO 2 R′, OR′, N(R′) 2 , SR′, NO 2 , halogen, CN, C(O)N(R′) 2 , NR′C(O)R′, SO 2 R′, SO 2 N(R) 2 , or NR′SO 2 R′;
y is 0 or 1;
T is a straight or branched C 1-4 alkylidene chain, wherein one methylene unit of T is optionally replaced by —O—, —NH—, or —S—;
each R′ is independently selected from hydrogen, C 1-4 aliphatic, or a 5-6 membered saturated, unsaturated, or aryl ring having 0-3 heteroatoms independently selected from nitrogen, oxygen, or sulfur, wherein:
R′ is substituted with 0-3 groups independently selected from halogen, oxo, R o , N(R o ) 2 , OR o , CO 2 R o , NR o C(O)R o , C(O)N(R o ) 2 , SO 2 R o , SO 2 N(R o ) 2 , or NR o , SO 2 R o , wherein:
each R o is independently selected from hydrogen, C 1-4 aliphatic, or a 5-6 membered saturated, unsaturated, or aryl ring having 0-3 heteroatoms independently selected from nitrogen, oxygen, or sulfur, and wherein:
two substituents on adjacent positions of R 1 may be taken together to form a 5-7 membered saturated, partially unsaturated, or aryl ring having 0-3 heteroatoms independently selected from nitrogen, oxygen, or sulfur;
Ar is a 3-8 membered saturated, unsaturated, or aryl ring, a 3-7 membered heterocyclic ring having 1-3 heteroatoms independently selected from nitrogen, oxygen, or sulfur, or a 5-6 membered heteroaryl ring having 1-3 heteroatoms independently selected from nitrogen, oxygen, or sulfur, wherein:
Ar is substituted with 0-3 groups independently selected from R′, oxo, CO 2 R′, OR′, N(R′) 2 , SR′, NO 2 , halogen, CN, C(O)N(R′) 2 , NR′C(O)R′, SO 2 R′, C(O)R′, SO 2 N(R′) 2 , or NR′SO 2 R′;
R 2 is selected from hydrogen or a C 1-3 aliphatic group; and
Ring A is a 5-6 membered heteroaryl ring having 1-4 heteroatoms independently selected from nitrogen, oxygen, or sulfur, provided that said ring has a hydrogen-bond acceptor in the position adjacent to the point of attachment to Ring B, wherein:
Ring A is substituted with 0-3 groups independently selected from R′, oxo, CO 2 R′, OR′, N(R′) 2 , SR′, NO 2 , halogen, CN, C(O)N(R′) 2 , NR′C(O)R′, SO 2 R′, SO 2 N(R′) 2 , or NR′SO 2 R′, and wherein:
two substituents on adjacent positions of Ring A may be taken together to form a 5-7 membered saturated, partially unsaturated, or aryl ring having 0-3 heteroatoms independently selected from nitrogen, oxygen, or sulfur.
2 . The compound according to claim 1 , wherein Ring A is selected from the following optionally substituted rings:
3 . The compound according to claim 2 , wherein Ring A is an optionally substituted ring selected from rings a, f, l, s, w, y, or z:
4 . The compound according to claim 1 , wherein:
R 1 is selected from an optionally substituted phenyl or 5-6 membered heteroaryl ring having 1-2 nitrogens.
5 . The compound according to claim 4 , wherein R 1 is an optionally substituted ring selected from pyrid-2-yl, pyrid-3-yl, pyrid-4-yl, pyrimidin-2-yl, pyrimidin-4-yl, pyrimidin-5-yl, pyrimidin-6-yl, imidazol-1-yl, imidazol-2-yl, imidazol-4-yl, or imidazol-5-yl.
6 . The compound according to claim 5 , wherein R 1 is substituted with 0-2 groups independently selected from halogen, oxo, R′, CO 2 R′, OR′, N(R′) 2 , SR′, C(O)N(R) 2 , NR′C(O)R′, SO 2 R′, SO 2 N(R′) 2 , or NR′SO 2 R′.
7 . The compound according to claim 6 , wherein R 2 is selected from methyl, ethyl, isopropyl, or cyclopropyl.
8 - 16 . (canceled)
17 . The compound according to claim 1 , wherein said compound is of formula
or a pharmaceutically acceptable salt thereof.
18 . (canceled)
19 . The compound according to claim 1 wherein R 2 is ethyl.
20 . A compound selected from the group consisting of:
and I-295.
21 . A composition comprising a compound according to claim 1 , and a pharmaceutically acceptable carrier, adjuvant, or vehicle.
22 - 24 . (canceled)
25 . A method of inhibiting gyrase and TopoIV activity in a patient, comprising the step of contacting said patient with a composition according to claim 21 .
26 . A method of decreasing bacterial quantity in a patient, comprising the step of administering to said patient a composition according to claim 21 .
27 . A method of treating, preventing, or lessening the severity of, a bacterial infection in a patient, comprising the step of administering to said patient a composition according to claim 21 .
28 . The method according to claim 27 , wherein the bacterial infection to be treated is characterized by the presence of one or more of the following: Streptococcus pneumoniae, Streptococcus pyogenes, Enterococcus faecalis, Enterococcus faecium, Klebsiella pneumoniae, Enterobacter sps. Proteus sps. Pseudomonas aeruginosa, E. coli, Serratia marcesens, Staphylococcus aureus, Coag. Neg. Staph, Haemophilus influenzae, Bacillus anthracis, Mycoplasma pneumoniae, Moraxella catarralis, Chlamydia pneumoniae, Legionella pneumophila, Staphylococcus epidermidis, Mycobacterium tuberculosis , or Helcoibacter pylori.
29 . The method according to claim 28 , wherein the bacterial infection to be treated is selected from one or more of the following: a urinary tract infection, a respiratory infection, pneumonia, prostatitis, a skin or soft tissue infection, an intra-abdominal infection, a blood stream infection, or an infection of febrile neutropenic patients.
30 . The method according to claim 29 , further comprising the step of administering to said patient an additional therapeutic agent either as part of a multiple dosage form together with said compound or as a separate dosage form.
31 . (canceled)Join the waitlist — get patent alerts
Track US2013023525A1 — get alerts on status changes and closely related new filings.
We store only your email — no account needed. See our privacy policy.