IP Library › Granted Patent US 7,432,277
Granted Patent B2
US 7,432,277 · App. 11/429,582 · Granted Oct 7, 2008

Phosphorus-containing macrocycles

Assignee: ARAID Gene Therapeutics, Inc.
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Quick Facts
Patent No.
US 7,432,277
App. No.
11/429,582
Granted
Oct 7, 2008
Kind
B2
Abstract

This invention concerns a new family of phosphorus-containing macrocycles containing various phosphonate- and phosphonate-containing moieties.

Claims (50)

1. A compound of the Formula I:

wherein:

A is independently —O—, —S— or —NR 2 —;

Q is V or VN(R)V; wherein V is independently an aliphatic, a heteroaliphatic, an aryl or a 5-14 membered heteroaryl moiety, having 1-4 heteroatoms selected from nitrogen, oxygen and sulfur;

J is:

each occurrence of X is independently H, —NR 2 R 5 , —OR 2 or halo;

one of R 7a and R 7b is H and the other is H, halo, —R A , —OR A , —SR A , —OC(O)R A , —OC(O)NR A R B , —NR A R B , —NR B C(O)R A , —NR B C(O)OR A , —NR B SO 2 R A , —OC(O)OR A , —NR B C(O)NR A R B or

—NR B SO 2 NR A R B ′; or R 7a and R 7b , taken together, are H in the tetraene moiety:

R A is R 2 , R B is OH or R 2 ;

R, R 2 and R 5 are independently selected from H, an aliphatic, a heteroaliphatic, an aryl and a 5-14 membered heteroaryl moiety having 1-4 heteroatoms selected from nitrogen, oxygen and sulfur;

R 28 is hydrogen, —COVH or COAQJ;

and n is 1 or 2;

wherein each aliphatic moiety contains 1-8 contiguous aliphatic carbon atoms, each heteroaliphatic moiety is an aliphatic moiety which contains an O, S, N, P or Si atom in place of one or more carbon atoms; and each of the foregoing aliphatic and heteroaliphatic moieties is independently branched or unbranched, or cyclic or acyclic, and unsubstituted or substituted with one or more groups selected from halogen, —YR 2 , —Y—C(═O)R 2 , —NR 2 C(═O)R 5 , —NR 2 C(═O)NR 5 , —NR 2 C(═O)OR 5 , —NR 2 C(═NH)NR 5 , —Y—C(═O)OR 2 , —Y—C(═O)NR 2 R 5 , —Y—C(═NR 2 )NR 2 R 5 , —COCOR 2 , —C(═O)(CH 2 ) r C(═O)R 2 , J, —CN, —S(═O)R 2 , —SO 2 R 2 , —SO 2 NR 2 R 5 , —NO 2 , —NR 5 SO 2 R 2 , —OSO 2 R 2 , —NR 5 SO 2 NR 2 R 5 , ═O, ═S, ═NR 2 , ═NNR 2 R 5 , ═NNHC(O)R 2 , ═NNHCO 2 R 2 , and ═NNHSO 2 R 2 , wherein Y is selected from a bond, —O—, NR 5 , and —S—, r is an integer of 1 to 4;

and each aryl or heteroaryl moiety is independently unsubstituted or substituted with one or more groups selected from halogen, —YR 2 , —Y—C(═O)R 2 , —NR 2 C(═O)R 5 , —NR 2 C(═O)NR 5 , —NR 2 C(═O)OR 5 , and —NR 2 C(═NR 2 )NR 5 , —Y—C(═O)OR 2 , —Y—C(═O)NR 2 R 5 , —Y—C(═NR 2 )NR 2 R 5 , —COCOR 2 , —C(═O)(CH 2 ) r C(═O)R 2 , J, —CN, —S(═O)R 2 , —SO 2 R 2 , —SO 2 NR 2 R 5 , —OSO 2 R 2 , —NO 2 , —NR 5 SO 2 R 2 and —NR 5 SO 2 NR 2 R; wherein Y is selected from a bond, —O—, NR 5 and —S—, r is an integer of 1 to 4.

2. A compound of the Formula II:

wherein:

A is independently —O—, —S— or —NR 2 —;

V is selected from the groups consisting of an aliphatic, a heteroaliphatic, an aryl and a 5-14 membered heteroaryl moiety, having 1-4 heteroatoms selected from nitrogen, oxygen and sulfur;

J is:

each occurrence of X is independently H, —NR 2 R 5 , —OR 2 or halo;

one of R 7a and R 7b is H and the other is H, halo, —R A , —OR A , —SR A , —OC(O)R A , —OC(O)NR A R B , —NR A R B , —NR B C(O)R A , —NR B C(O)OR A , —NR B SO 2 R A , —OC(O)OR A , —NR B C(O)NR A R B , or

—NR B SO 2 NR A R B ′; or R 7a and R 7b , taken together, are H in the tetraene moiety:

R A is R 2 , R B is OH or R 2 , (in some cases one or both of R A and R B is H);

R, R 2 and R 5 are independently selected from H, an aliphatic, a heteroaliphatic, an aryl and a 5-14 membered heteroaryl moiety having 1-4 heteroatoms selected from nitrogen, oxygen and sulfur;

R 28 is hydrogen, —COVH or COAQJ;

and n is 1 or 2;

wherein each aliphatic moiety contains 1-8 contiguous aliphatic carbon atoms, each heteroaliphatic moiety is an aliphatic moiety which contains an O, S, N, P or Si atom in place of one or more carbon atoms; and each of the foregoing aliphatic and heteroaliphatic moieties is independently branched or unbranched, or cyclic or acyclic, and unsubstituted or substituted with one or more groups selected from halogen, —YR 2 , —Y—C(═O)R 2 , —NR 2 C(═O)R 5 , —NR 2 C(═O)NR 5 , —NR 2 C(═O)OR 5 , —NR 2 C(═NH)NR 5 , —Y—C(═O)OR 2 , —Y—C(═O)NR 2 R 5 , —Y—C(═NR 2 )NR 2 R 5 , —COCOR 2 , —C(═O)(CH 2 ) r C(═O)R 2 , J, —CN, —S(═O)R 2 , —SO 2 R 2 , —SO 2 NR 2 R 5 , —NO 2 , —NR 5 SO 2 R 5 , —OSO 2 R 2 , —NR 5 SO 2 NR 2 R 5 , ═S, ═NR 2 , ═NNR 2 R 5 , ═NNHC(O)R 2 , ═NNHCO 2 R 2 , and ═NNHSO 2 R 2 , wherein Y is selected from a bond, —O—, NR 5 and —S—, r is an integer of 1 to 4;

and each aryl or heteroaryl moiety is independently unsubstituted or substituted with one or more groups selected from halogen, —YR 2 , —Y—C(═O)R 2 , —NR 2 C(═O)R 5 , —NR 2 C(═O)NR 5 , —NR 2 C(═O)OR 5 , and —NR 2 C(═NR 2 )NR 5 , —Y—C(═O)OR 2 , —Y—C(═O)NR 2 R 5 , —Y—C(═NR 2 )NR 2 R 5 , —COCOR 2 , —C(═O)(CH 2 ) r C(═O)R 2 , J, —CN, —S(═O)R 2 , —SO 2 R 2 , —SO 2 NR 2 R 5 , —OSO 2 R 2 , —NO 2 , —NR 5 SO 2 R 2 and —NR 5 SO 2 NR 2 R; wherein Y is selected from a bond, —O—, NR 5 and —S—, r is an integer of 1 to 4.

3. The compound of claim 2 having the formula II(a):

in which m is an integer from 2 through 8.

4. The compound of claim 3 having the formula II(b):

5. The compound of claim 3 having the formula II(d):

6. The compound of claim 2 having the formula II(e):

wherein Z is CH or N.

7. The compound of any of claims 3 , 4 and 6 wherein one or both of R and R 2 groups are H.

8. The compound of any of claims 3 , 4 and 6 wherein one or both R and R 2 groups are C1-C8 alkyl groups.

9. The compound of any of claims 3 , 4 and 6 wherein one or both R and R 2 groups are CH 3 .

10. The compound of any of claims 1 - 6 wherein n is 2; R 28 is H; R 7a is OMe and R 7b is H.

11. The compound of claim 4 having the formula II(f):

wherein JV— is selected from the following:

and wherein p is 0, 1, 2, 3, 4 or 5and Z is N or CH.

12. The compound of claim 1 of the formula III(a):

13. The compound of claim 12 wherein A is O or NR 2 .

14. The compound of claim 12 wherein V is a 1-8-carbon alkyl moiety.

15. The compound of claim 12 wherein V is an aryl or a 5-14 membered heteroaryl moiety having 1-4 heteroatoms selected from nitrogen, oxygen, or sulfur.

16. The compound of claim 12 of the formula III(b):

wherein JVNR 2 —C(O)— is selected from the following:

17. The compound of claim 12 of the formula III(c):

wherein JVOC(O)— is selected from:

18. A composition comprising a compound of claim 1 , together with a pharmaceutically acceptable vehicle and optionally containing one or more pharmaceutically acceptable excipients.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 23, 2021
From: ARIAD PHARMACEUTICALS, INC.
To: TAKEDA PHARMACEUTICAL COMPANY LIMITED
Reel/Frame 056637/0879 →
MERGER Recorded Mar 25, 2009
From: ARIAD GENE THERAPEUTICS, INC.
To: ARIAD PHARMACEUTICALS, INC.
Reel/Frame 022449/0671 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 24, 2006
From: METCALF III, CHESTER A.; ROZAMUS, LEONARD W.; WANG, YIHAN; THOMAS, R. MATHEW; ZOU, DONG; BERSTEIN, DAVID L.
To: ARIAD GENE THERAPEUTICS, INC.
Reel/Frame 018121/0891 →
Continuity (11)
Continuation In Part 1088916300 · Jul 12, 2004
Continuation In Part 1086214900 · Jun 4, 2004
Continuation In Part 1063505400 · Aug 6, 2003
Continuation In Part 1035715200 · Feb 3, 2003
Provisional Application 6071185900 · Aug 26, 2005
Provisional Application 6048636700 · Jul 11, 2003
Provisional Application 6043393000 · Dec 17, 2002
Provisional Application 6042838300 · Nov 22, 2002
Provisional Application 6042692800 · Nov 15, 2002
Provisional Application 6035325200 · Feb 1, 2002
Related Publication 20060264405A1 · Nov 23, 2006