IP Library Granted Patent US 9,029,368
Granted Patent B2
US 9,029,368 · App. 14/362,026 · Granted May 12, 2015

3,7-disubstituted octahydro-2H-pyrido[4,3-E][1,3]oxazin-2-one antibiotics

Inventors: Christian Hubschwerlen (Durmenach, FR); Georg Rueedi (Allschwil, CH); Jean-Philippe Surivet (Kembs, FR); Cornelia Zumbrunn Acklin (Basel, CH)
Assignee: Actelion Pharmaceuticals Ltd.
C07D498/04C07D513/04
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 9,029,368
App. No.
14/362,026
Granted
May 12, 2015
Kind
B2
Abstract

The invention relates to antibacterial compounds of formula I wherein G and K are as defined in the description; and salts of such compounds.

Claims (87)

1. A compound of formula I comprising a relative trans configuration of the octahydro-pyrido[4,3-e][1,3]oxazinone moiety

wherein

K represents the group Ka

wherein R 1a represents alkoxy, halogen or cyano;

one or two of U a , V a , W a represent(s) N and the remaining two or one of U a , V a , W a represent(s) CH;

X a represents CR a wherein R a represents hydrogen or halogen;

A represents CHR b wherein R b represents hydrogen or hydroxyl;

or K represents the group Kb

wherein R 1b represents hydrogen, alkoxy, halogen or cyano;

one or two of U b , V b and W b represent(s) N and the remaining two or one of U b , V b W b represent(s) CH;

or K represents the group Kc or Kd wherein

wherein R 1c and R 1d independently represent H or F;

V c , V d , W e and W d independently represent CH or N; and

G represents one of the groups Ga, Gb, Gc and Gd

wherein M represents CH or N; and Q and Q′ independently represent O or S;

or a salt of the compound.

2. The compound according to claim 1 , wherein K represents the group Ka or Kb;

or a salt of the compound.

3. The compound according to claim 2 , wherein K represents the group Ka wherein R1a represents methoxy, or wherein K represents the group Kb wherein R1b represents methoxy;

or a salt of the compound.

4. The compound according to claim 2 , wherein K represents the group Ka;

or a salt of the compound.

5. The compound according to claim 1 , wherein A represents CHRb wherein Rb represents hydrogen;

or a salt of the compound.

6. The compound according to claim 1 , wherein A represents CHRb wherein Rb represents hydroxyl, and the absolute configuration of the carbon atom to which Rb is attached to is (R);

or a salt of the compound.

7. The compound according to claim 2 , wherein K represents the group Kb;

or a salt of the compound.

8. The compound according to claim 1 , wherein G represents a group of

wherein

M represents CH and Q′ represent O or S; or

M represents N and Q′ represents S; and

Q represents O or S;

or a salt of the compound.

9. The compound according to claim 1 , wherein:

K represents the group Ka

wherein R 1a represents methoxy;

U a and W a each represent N and V a and X a each represent CH;

X a represents CR a wherein R a represents fluorine;

A represents CHR b wherein R b represents hydrogen or hydroxyl;

or K represents the group Kb

wherein R 1b represents methoxy;

U b represents N, V b represents CH and W b represents CH or N; and

G represents one of the groups Gb and Gc

wherein Q represents O or S;

or a salt of the compound.

10. The compound according to claim 1 , wherein the compound is:

(4aR,8aR)-3-(2,3-dihydro-benzo[1,4]dioxin-6-yl)-7-[2-(3-fluoro-6-methoxy-[1,5]naphthyridin-4-yl)-ethyl]-octahydro-pyrido[4,3-e][1,3]oxazin-2-one;

(4aS,8aS)-3-(2,3-dihydro-benzo[1,4]dioxin-6-yl)-7-[2-(3-fluoro-6-methoxy-[1,5]naphthyridin-4-yl)-ethyl]-octahydro-pyrido[4,3-e][1,3]oxazin-2-one;

(4aR*,8aR*)-3-(2,3-dihydro-benzo[1,4]dioxin-6-yl)-7-[2-hydroxy-2-(6-methoxy-[1,5]naphthyridin-4-yl)-ethyl]-octahydro-pyrido[4,3-e][1,3]oxazin-2-one;

(4aR*,8aR*)-3-(2,3-dihydro-benzo[1,4]dioxin-6-yl)-7-[2-(6-methoxy-[1,5]naphthyridin-4-yl)-ethyl]-octahydro-pyrido[4,3-e][1,3]oxazin-2-one;

(4aR*,8aR*)-7-[2-(3-fluoro-6-methoxy-[1,5]naphthyridin-4-yl)-ethyl]-3-(3-oxo-3,4-dihydro-2H-benzo[1,4]oxazin-6-yl)-octahydro-pyrido[4,3-e][1,3]oxazin-2-one;

(4aR*,8aR*)-3-(2,3-dihydro-benzo[1,4]dioxin-6-yl)-7-[2-(3-fluoro-6-methoxy-[1,5]naphthyridin-4-yl)-2-hydroxy-ethyl]-octahydro-pyrido[4,3-e][1,3]oxazin-2-one;

(4aR*,8aR*)-7-[2-(3-fluoro-6-methoxy-[1,5]naphthyridin-4-yl)-ethyl]-3-(3-oxo-3,4-dihydro-2H-benzo[1,4]thiazin-6-yl)-octahydro-pyrido[4,3-e][1,3]oxazin-2-one;

(4aR*,8aR*)-3-(2,3-dihydro-benzo[1,4]dioxin-6-yl)-7-[2-(7-methoxy-2-oxo-2H-quinolin-1-yl)-ethyl]-octahydro-pyrido[4,3-e][1,3]oxazin-2-one;

(4aR*,8aR*)-3-(2,3-dihydro-benzo[1,4]dioxin-6-yl)-7-[2-(7-methoxy-2-oxo-2H-quinoxalin-1-yl)-ethyl]-octahydro-pyrido[4,3-e][1,3]oxazin-2-one;

(4aR*,8aR*)-3-(2,3-dihydro-benzo[1,4]dioxin-6-yl)-7-[2-(7-methoxy-2-oxo-2H-[1,8]naphthyridin-1-yl)-ethyl]-octahydro-pyrido[4,3-e][1,3]oxazin-2-one;

(4aR*,8aR*)-3-(2,3-dihydro-benzo[1,4]dioxin-6-yl)-7-[2-(6-methoxy-3-oxo-3H-pyrido[2,3-b]pyrazin-4-yl)-ethyl]-octahydro-pyrido[4,3-e][1,3]oxazin-2-one;

(4aR*,8aR*)-3-(2,3-dihydro-benzo[1,4]dioxin-6-yl)-7-[2-(3-methoxy-6-oxo-6H-pyrido[2,3-b]pyrazin-5-yl)-ethyl]-octahydro-pyrido[4,3-e][1,3]oxazin-2-one;

(4aR*,8aR*)-3-(2,3-dihydro-benzo[1,4]dioxin-6-yl)-7-[(R)-2-(3-fluoro-6-methoxy-[1,5]naphthyridin-4-yl)-2-hydroxy-ethylkoctahydro-pyrido[4,3-e][1,3]oxazin-2-one;

(4aS,8aS)-3-(2,3-dihydro-benzo[1,4]dioxin-6-yl)-7-[(S)-2-(3-fluoro-6-methoxy-[1,5]naphthyridin-4-yl)-2-hydroxy-ethyl]-octahydro-pyrido[4,3-e][1,3]oxazin-2-one;

(4aR,8aR)-3-(2,3-dihydro-benzo[1,4]dioxin-6-yl)-7-[(S)-2-(3-fluoro-6-methoxy-[1,5]naphthyridin-4-yl)-2-hydroxy-ethyl]-octahydro-pyrido[4,3-e][1,3]oxazin-2-one;

(4aR*,8aR*)-3-(2,3-dihydro-benzo[1,4]dioxin-6-yl)-7-[2-(7-fluoro-2-methoxy-quinolin-8-yl)-2-hydroxy-ethyl]-octahydro-pyrido[4,3-e][1,3]oxazin-2-one;

(4aR*,8aR*)-3-(2,3-dihydro-benzo[1,4]dioxin-6-yl)-7-[2-(6-fluoro-3-methoxy-quinoxalin-5-yl)-2-hydroxy-ethyl]-octahydro-pyrido[4,3-e][1,3]oxazin-2-one;

(4aR*,8aR*)-3-(2,3-dihydro-benzo[1,4]dioxin-6-yl)-7-[2-hydroxy-2-(3-methoxy-quinoxalin-5-yl)-ethyl]-octahydro-pyrido[4,3-e][1,3]oxazin-2-one;

(4aR*,8aR*)-7-[2-(3-fluoro-6-methoxy[1,5]naphthyridn-4-yl)-ethyl]-3-(3-oxo-3,4-dihydro-2H-pyrido[3,2-b][1,4]oxazin-6-yl)-octahydro-pyrido[4,3-e][1,3]oxazin-2-one;

(4aR,8aR)-7-[2-(3-fluoro-6-methoxy-[1,5]naphthyridin-4-yl)-ethyl]-3-(3-oxo-3,4-dihydro-2H-pyrido[3,2-b)][1,4]thiazin-6-yl)-octahydro-pyrido[4,3-e][1,3]oxazin-2-one;

(4aS,8aS)-7-[2-(3-fluoro-6-methoxy-[1,5]naphthyridin-4-yl)-ethyl]-3-(3-oxo-3,4-dihydro-2H-pyrido[3,2-b][1,4]thiazin-6-yl)-octahydro-pyrido[4,3-e][1,3]oxazin-2-one;

(4aR*,8aR*)-3-(2,3-dihydro-[1,4]dioxino[2,3-b]pyridin-7-yl)-7-[2-(3-fluoro-6-methoxy-[1,5]naphthyridin-4-yl)-ethylkoctahydro-pyrido[4,3-e][1,3]oxazin-2-one;

(4aR*,8aR*)-3-(6,7-dihydro-[1,4]dioxino[2,3-c]pyridazin-3-yl)-7-[2-(3-fluoro-6-methoxy-[1,5]naphthyridin-4-yl)-ethyl]-octahydro-pyrido[4,3-e][1,3]oxazin-2-one;

(4aR*,8aR*)-3-(2,3-dihydro-[1,4]dioxino[2,3-c]pyridin-7-yl)-7-[2-(3-fluoro-6-methoxy-[1,5]naphthyridin-4-yl)-ethyl]-octahydro-pyrido[4,3-e][1,3]oxazin-2-one;

(4aR*,8aR*)-7-[2-(7-methoxy-2-oxo-2H-[1,8]naphthyridin-1-yl)-ethyl]-3-(3-oxo-3,4-dihydro-2H-pyrido[3,2-b][1,4]oxazin-6-yl)-octahydro-pyrido[4,3-e][1,3]oxazin-2-one;

(4aR*,8aR*)-7-[2-(7-methoxy-2-oxo-2H-[1,8]naphthyridin-1-yl)-ethyl]-3-(3-oxo-3,4-dihydro-2H-pyrido[3,2-b][1,4]thiazin-6-yl)-octahydro-pyrido[4,3-e][1,3]oxazin-2-one;

(4aR*,8aR*)-3-(6,7-dihydro-8-oxa-5-thia-1,2-diaza-naphthalen-3-yl)-7-[2-(3-fluoro-6-methoxy-[1,5]naphthyridin-4-yl)-ethyl]-octahydro-pyrido[4,3-e][1,3]oxazin-2-one;

(4aR*,8aR*)-3-(6,7-dihydro-8-oxa-5-thia-1,2-diaza-naphthalen-3-yl)-7-[2-(6-methoxy-3-oxo-3H-pyrido[2,3-b]pyrazin-4-yl)-ethyl]-octahydro-pyrido[4,3-e][1,3]oxazin-2-one;

(R)-2-[(4aR*,8aR*)-3-(2,3-dihydro-benzo[1,4]dioxin-6-yl)-2-oxo-octahydro-pyrido[4,3-e][1,3]oxazin-7-ylmethyl]-9-fluoro-1,2-dihydro-pyrrolo[3,2,1-ij]quinolin-4-one;

4-[(4aR*,8aR*)-3-(2,3-dihydro-benzo[1,4]dioxin-6-yl)-2-oxo-octahydro-pyrido[4,3-e][1,3]oxazin-7-ylmethyl]-3-fluoro-4,5-dihydro-pyrrolo[3,2,1-de][1,5]naphthyridin-7-one;

(4aR*,8aR*)-7-(2-(7-methoxy-2-oxo-1,8-naphthyridin-1(2H)-yl)ethyl)-3-(3-oxo-3,4-dihydro-2H-benzo[b][1,4]thiazin-6-yl)octahydro-2H-pyrido[4,3-e][1,3]oxazin-2-one;

(4aR*,8aR*)-7-((2RS)-2-(3-fluoro-6-methoxy-1,5-naphthyridin-4-yl)-2-hydroxyethyl)-3-(3-oxo-3,4-dihydro-2H-benzo[b][1,4]oxazin-6-yl)octahydro-2H-pyrido[4,3-e][1,3]oxazin-2-one;

(4aR*,8aR*)-7-(((R)-9-fluoro-4-oxo-2,4-dihydro-1H-pyrrolo[3,2,1-ij]quinolin-2-yl)methyl)-3-(3-oxo-3,4-dihydro-2H-pyrido[3,2-b][1,4]oxazin-6-yl)octahydro-2H-pyrido[4,3-e][1,3]oxazin-2-one; or

(4aR*,8aR*)-7-(2-(7-methoxy-2-oxo-1,8-naphthyridin-1(2H)-yl)ethyl)-3-oxo-3,4-dihydro-2H-benzo[b][1,4]oxazin-6-yl)octahydro-2H-pyrido[4,3-e][1,3]oxazin-2-one;

or a salt of the compound.

11. A pharmaceutical composition comprising as an active principle the compound according to claim 1 , or a pharmaceutically acceptable salt thereof, and at least one therapeutically inert excipient.

12. A method of treating a bacterial infection comprising administering to a subject in need thereof an effective amount of the compound according to claim 1 , wherein the bacterial infection is a respiratory tract infection, otitis media, meningitis, skin and soft tissue infection, pneumonia, bacteremia, endocarditis, intraabdominal infection, gastrointestinal infection, Clostridium difficile infection, urinary tract infection, sexually transmitted infection, foreign body infection, osteomyelitis, lyme disease, topical infection, opthalmological infection, tuberculosis, tropical disease or combinations thereof.

13. The method according to claim 12 , wherein the bacterial infection is respiratory tract infection, otitis media, meningitis, skin and soft tissue infection, pneumonia, bacteremia, or combinations thereof.

14. The method according to claim 12 , wherein the bacterial infection is caused by Staphylococcus aureus.

15. A method of treating a bacterial infection caused by Staphylococcus aureus bacteria comprising administering to a subject in need thereof an effective amount of the compound according to claim 1 .

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 3, 2014
From: HUBSCHWERLEN, CHRISTIAN; RUEEDI, GEORG; SURIVET, JEAN-PHILIPPE; ZUMBRUNN ACKLIN, CORNELIA
To: ACTELION PHARMACEUTICALS LTD
Reel/Frame 033017/0281 →
Priority Claims (1)
WO PCT/IB2011/055383 · Nov 30, 2011 · international
Continuity (1)
Related Publication 20140309218A1 · Oct 16, 2014