IP Library Granted Patent US 10,849,883
Granted Patent B2
US 10,849,883 · App. 16/073,934 · Granted Dec 1, 2020

Benzopyrazole compounds and analogues thereof

Inventors: Pravin L. Kotian (Hoover, AL); Yarlagadda S. Babu (Birmingham, AL); Weihe Zhang (Vestavia, AL); Lakshminarayana Vogeti (Lawrence, KS); Minwan Wu (Vestavia Hills, AL); Venkat R. Chintareddy (Vestavia Hills, AL); Krishnan Raman (Birmingham, AL)
Assignee: BioCryst Pharmaceuticals, Inc.
A61K31/416A61P9/00A61P13/10A61P21/04A61P25/28A61P37/06C07D209/12C07D209/40C07D209/42C07D209/48C07D231/56C07D401/04C07D401/06C07D401/12C07D401/14C07D403/04C07D403/06C07D403/12C07D405/12C07D471/04C07D487/04
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Quick Facts
Patent No.
US 10,849,883
App. No.
16/073,934
Granted
Dec 1, 2020
Kind
B2
Abstract

Disclosed are compounds of formula I, and pharmaceutically acceptable salts thereof. The compounds are inhibitors of the complement system. Also provided are pharmaceutical compositions comprising a compound of formula I, and methods involving use of the compounds and compositions in the treatment and prevention of diseases and conditions characterized by aberrant complement system activity.

Claims (53)

1. A compound represented by Formula (I), or a pharmaceutically acceptable salt thereof:

wherein, independently for each occurrence:

R 1 represents substituted aryl, heteroaryl, cycloalkyl, or heterocycloalkyl;

R 2 and R 3 each independently represent H;

R 4 represents H or optionally substituted alkyl, alkenyl, alkynyl, cycloalkyl, (cycloalkyl)alkyl, heterocycloalkyl, (heterocycloalkyl)alkyl, aralkyl, heteroaralkyl, hydroxyalkyl, or haloalkyl;

X represents CH 2 ;

Y is absent or represents CH 2 , C(O), CR 15 R 16 , S(O) 2 , or optionally substituted (C 3 -C 7 )cycloalkylene, arylene, or heteroarylene;

R a represents H or optionally substituted (C 1 -C 6 )alkyl, (heterocycloalkyl)alkyl, or (C 3 -C 7 )cycloalkyl;

m is an integer from 1-6;

n is 0 or 1;

R 15 and R 16 are each independently selected from the group consisting of H, hydroxy, halogen, —C(O)OR 17 , —C(O)NR 17 R 18 , —NR 17 R 18 , alkyl, hydroxyalkyl, haloalkyl, alkoxyalkyl, aryl, aralkyl, heteroaryl, heteroaralkyl, cycloalkyl, (cycloalkyl)alkyl, heterocycloalkyl, and (heterocycloalkyl)alkyl, wherein alkyl, aryl, aralkyl, heteroaryl, heteroaralkyl, cycloalkyl, (cycloalkyl)alkyl, heterocycloalkyl, and (heterocycloalkyl)alkyl are optionally substituted with one or more substituents selected from the group consisting of —CN, —OR 17 , —NR 17 R 18 , halo, and alkyl;

or R 15 and R 16 may be taken together with the intervening atom to form an optionally substituted carbocyclic or heterocyclic ring;

R 17 and R 18 are each independently selected from the group consisting of H, alkyl, haloalkyl, hydroxyalkyl, alkoxyalkyl, aryl, aralkyl, heteroaryl, heteroaralkyl, cycloalkyl, (cycloalkyl)alkyl, heterocycloalkyl, and (heterocycloalkyl)alkyl;

or R 17 and R 18 , when attached to the same atom, may be taken together with the intervening atom to form an optionally substituted heterocyclic ring;

represents

Z 1 represents N;

Z 2 represents N;

Z 3 represents C;

Z 4 represents CR 8 ;

Z 5 represents CR 5 ;

Z 6 represents CR 6 ;

Z 7 represents CR 9 ;

R 5 and R 6 each independently represent H, halogen, —CN, —NO 2 , —OR 13 , —NR 13 R 14 , —C(O)R 13 , —C(O)OR 13 , —C(O)NR 13 R 14 , —OC(O)R 13 , —NR 13 C(O)R 14 , —OC(O)NR 13 R 14 , —OC(O)OR 13 , —NR 13 C(O)OR 14 , —NR 13 C(O)NR 13 R 14 , —OS(O) p (R 13 ), —NR 13 S(O) p (R 14 ), or optionally substituted alkyl, alkenyl, alkynyl, haloalkyl, aralkyl, heteroaralkyl, heteroaryl, aryl, cycloalkyl, (cycloalkyl)alkyl, heterocycloalkyl, or (heterocycloalkyl)alkyl;

L represents —H, —CN, —C(O)R 7 , —CH(OH)R 7 , or —S(O) p (alkyl);

R 7 , independently for each occurrence, represents H, NH 2 , CH 3 , OH, CF 3 , CH 2 OH, (C 1 -C 6 )alkyl, hydroxy(C 1 -C 6 )alkyl, (C 1 -C 6 )alkoxy(C 1 -C 6 )alkyl, halo(C 1 -C 6 )alkyl, NH(C 1 -C 6 )alkyl, N((C 1 -C 6 )alkyl) 2 ;

R 8 and R 9 each independently represent H, halogen, —OR 13 , —NR 13 R 14 , —C(O)R 13 , —C(O)OR 13 , —C(O)NR 13 R 14 , —OC(O)R 13 , —NR 13 C(O)R 14 , —OC(O)NR 13 R 14 , —OC(O)OR 13 , —NR 13 C(O)OR 14 , —NR 13 C(O)NR 13 R 14 , —OS(O) p (R 13 ), —NR 13 S(O) p (R 14 ), or optionally substituted alkyl, alkenyl, alkynyl, haloalkyl, aralkyl, heteroaralkyl, heteroaryl, or aryl;

or R 5 and R 8 , or R 5 and R 6 , or R 6 and R 9 may be taken together with the intervening atoms to form an optionally substituted heterocyclic or carbocyclic ring;

R 13 and R 14 , independently for each occurrence, represent H or optionally substituted alkyl, alkenyl, alkynyl, aryl, aralkyl, heteroaryl, heteroaralkyl, cycloalkyl, (cycloalkyl)alkyl, heterocycloalkyl, or (heterocycloalkyl)alkyl; or, when R 13 and R 14 are attached to the same atom, R 13 and R 14 taken together with the atom may form an optionally substituted heterocyclic ring; and

p is 0, 1, or 2.

2. The compound of claim 1 , wherein n is 1.

3. The compound of claim 1 , wherein R 1 represents aryl or heteroaryl, substituted by one or more substituents independently selected from the group consisting of halogen, —CN, alkoxy, haloalkoxy, haloalkyl, dialkylamino, heterocycloalkyl, aryl, and heteroaryl; or R 1 represents aryl or heteroaryl, substituted by one or more substituents, at least one of which is halogen.

4. The compound of claim 1 , wherein Y is absent, Y is CH 2 , or Y is CR 15 R 16 .

5. The compound of claim 4 , wherein R 15 and R 16 are selected from the group consisting of H, alkyl, hydroxyalkyl, haloalkyl, alkoxyalkyl, aralkyl, heteroaralkyl (cycloalkyl)alkyl, and (heterocycloalkyl)alkyl;

wherein alkyl, aryl, aralkyl, heteroaryl, heteroaralkyl, cycloalkyl, (cycloalkyl)alkyl, heterocycloalkyl, and (heterocycloalkyl)alkyl are optionally substituted with one or more substituents selected from the group consisting of —CN, —OR 17 , —NR 17 R 18 , halo, and alkyl; and

further wherein R 17 and R 18 are each independently selected from the group consisting of H and alkyl.

6. The compound of claim 1 , wherein R 4 represents H or optionally substituted alkyl, cycloalkyl, (cycloalkyl)alkyl, heterocycloalkyl, aralkyl, hydroxyalkyl, or haloalkyl.

7. The compound of claim 1 , wherein R 4 represents H or optionally substituted alkyl or cycloalkyl.

8. The compound of claim 1 , wherein R 1 is H.

9. The compound of claim 1 , wherein m is 1.

10. The compound of claim 1 , wherein L represents —C(O)R 7 .

11. The compound of claim 1 , having the structure of Formula (Ia):

12. The compound of claim 11 , wherein Z 4 and Z 7 each represent CH.

13. The compound of claim 11 , wherein Z 5 represents CR 5 ; and Z 6 represents CR 6 ; and

R 5 and R 6 each independently represent H, halogen, —NR 13 R 14 , —C(O)R 13 , —C(O)OR 13 , —C(O)NHR 14 , —NHC(O)NR 13 R 14 , NHS(O) 2 (R 14 ), or optionally substituted alkyl, alkenyl, alkynyl, heteroaryl, or aryl.

14. The compound of claim 13 , wherein R 5 and R 6 each independently represent H or alkyl, alkenyl, alkynyl, heteroaryl, or aryl, optionally substituted with one or more substituents selected from the group consisting of aryl, heteroaryl, silyl, alkyl, amino, alkylamino, dialkylamino, —C(O)(alkyl), and halogen.

15. The compound of claim 13 , wherein R 13 and R 14 , independently for each occurrence, represent H or optionally substituted aryl, aralkyl, heteroaryl, heteroaralkyl, cycloalkyl, or (cycloalkyl)alkyl.

16. The compound of claim 10 , wherein R 7 represents NH 2 , CH 3 , or CF 3 .

17. The compound of claim 10 , wherein R 7 represents NH 2 .

18. The compound of claim 1 , or a pharmaceutically acceptable salt thereof, selected from the following table:

19. The compound of claim 1 , or a pharmaceutically acceptable salt thereof, selected from the following table:

20. A pharmaceutical composition, comprising a compound of claim 1 , or a pharmaceutically acceptable salt thereof; and a pharmaceutically acceptable carrier.

21. A method of treating a disease or condition characterized by aberrant complement system activity, comprising administering to a subject in need thereof a therapeutically effective amount of a compound of claim 1 , or a pharmaceutically acceptable salt thereof;

wherein the disease or condition characterized by aberrant complement system activity is selected from the group consisting of paroxysmal nocturnal hemoglobinuria, atypical hemolytic uremic syndrome, organ transplant rejection, myasthenia gravis, neuromyelitis optica, membranoproliferative glomerulonephritis, dense-deposit disease, cold agglutinin disease, and catastrophic antiphospholipid syndrome.

Assignments (5)
SECURITY INTEREST Recorded Jan 23, 2026
From: BIOCRYST PHARMACEUTICALS, INC.
To: WILMINGTON TRUST, NATIONAL ASSOCIATION
Reel/Frame 074485/0651 →
RELEASE OF GRANT OF SECURITY INTEREST IN PATENTS Recorded Apr 18, 2023
From: ATHYRIUM OPPORTUNITIES III CO-INVEST 1 LP
To: BIOCRYST PHARMACEUTICALS, INC.
Reel/Frame 063362/0550 →
SECURITY INTEREST Recorded Dec 17, 2020
From: BIOCRYST PHARMACEUTICALS, INC.
To: ATHYRIUM OPPORTUNITIES III CO-INVEST 1 LP
Reel/Frame 054800/0634 →
RELEASE OF SECURITY INTEREST Recorded Dec 16, 2020
From: MIDCAP FINANCIAL TRUST, AS AGENT
To: BIOCRYST PHARMACEUTICALS, INC.; MDCP, LLC
Reel/Frame 054774/0446 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 12, 2018
From: KOTIAN, PRAVIN L.; BABU, YARLAGADDA S.; ZHANG, WEIHE; VOGETI, LAKSHMINARAYANA; WU, MINWAN; CHINTAREDDY, VENKAT R.; RAMAN, KRISHNAN
To: BIOCRYST PHARMACEUTICALS, INC.
Reel/Frame 046852/0876 →