US2021252008A1PendingUtilityA1

Biaryl compositions and methods for modulating a kinase cascade

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Assignee: ATHENEX INCPriority: Dec 28, 2004Filed: Jan 19, 2021Published: Aug 19, 2021
Est. expiryDec 28, 2024(expired)· nominal 20-yr term from priority
C07D 213/56A61P 35/00A61P 37/00C07D 213/74C07D 401/12A61K 31/495A61P 3/10A61K 31/5377A61P 27/16C07D 213/89C07C 233/13C07D 239/26C07C 233/22C07D 403/04C07D 239/34A61P 37/02A61P 27/02A61P 19/10A61P 9/10A61P 35/04A61P 31/20A61P 25/00A61P 9/00A61P 17/06A61K 9/0053A61P 31/12A61P 3/04C07D 213/64
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Claims

Abstract

The invention relates to compounds and methods for modulating one or more components of a kinase cascade.

Claims

exact text as granted — not AI-modified
1 . A compound according to Formula IA 
       
         
           
           
               
               
           
         
       
       or a salt, solvate, hydrate, or prodrug thereof, wherein: T is absent, CR 12 R 13 , C(O), O, S, S(O), S(O) 2 , NR 14 , C(R 15 R 16 )C(R 17 R 18 ), CH 2 O, or OCH 2 ;
 X y  is CZ, CY, N, or N—O; 
 X z  is CZ, CY, N, or N—O; 
 at least one of X y  and X z  is CZ; 
 Y is selected from hydrogen, hydroxyl, halogen, lower (C 1 , C 2 , C 3 , C 4 , C 5 , or C 6 ) alkyl, C 1 , C 2 , C 3 , C 4 , C 5 , or C 6  alkoxy, O-lower (C 1 , C 2 , C 3 , C 4 , C 5 , or C 6 ) alkyl-aryl, and O-benzyl; 
 X a  is CR a  or N, or N—O; 
 X b  is CR b , N, or N—O; 
 X c  is CR c  or N, or N—O; 
 X d  is CR d  or N, or N—O; 
 X e  is CR e , N, or N—O; 
 R a , R b , R c , R d , R e , R 4 , R 5 , and R 6  are, independently, hydrogen, hydroxyl, halogen, P, C 1 , C 2 , C 3 , C 4 , C 5 , or C 6  alkyl, C 1 , C 2 , C 3 , C 4 , C 5 , or C 6  alkoxy, O-lower (C 1 , C 2 , C 3 , C 4 , C 5 , or C 6 ) alkyl-aryl, O-benzyl, C 1 , C 2 , C 3 , C 4 , C 5 , or C 6  alkyl-OH, COOH, COO-lower (C 1 , C 2 , C 3 , C 4 , C 5 , or C 6 ) alkyl, SO 2 H, SO 2 -lower (C 1 , C 2 , C 3 , C 4 , C 5 , or C 6 ) alkyl, 
 
       
         
           
           
               
               
           
         
       
       wherein W is H, or C 1 , C 2 , C 3 , C 4 , C 5 , or C 6  alkyl, C 1 , C 2 , C 3 , C 4 , C 5 , or C 6  alkyl-aryl;
 P is SO 3 H, OSO 3 H, OPO 3 H 2 , OPO 3 H 2 , NH 2 , NHR 19 , NHR 2 OR 21 , 
 
       
         
           
           
               
               
           
         
       
       tetrazole, O-lower (C 1 , C 2 , C 3 , C 4 , C 5 , or C 6 ) alkyl-K, O—C(O)-lower (C 1 , C 2 , C 3 , C 4 , C 5 , or C 6 ) alkyl-L, NH-lower (C 1 , C 2 , C 3 , C 4 , C 5 , or C 6 ) alkyl-M, or O-aryl-Q, further wherein lower (C 1 , C 2 , C 3 , C 4 , C 5 , or C 6 ) alkyl is linear or branched alkyl;
 K is C(O)NH 2 , COOH, SO 3 H, OSO 3 H, PO 3 H 2 , OPO 3 H 2 , NH 2 , NHR 19 , NR 19 R 20 , SO 2 R 21 , glycoside, lower C 1 , C 2 , C 3 , C 4 , C 5 , C 6  alkoxy, or 
 
       
         
           
           
               
               
           
         
         L is aryl, OH, C(O)NH 2 , COOH, SO 3 H, OSO 3 H, PO 3 H 2 , OPO 3 H 2 , NH 2 , NHR 19 , NR 19 R 20 , SO 2 R 21 , glycoside, lower C 1 , C 2 , C 3 , C 4 , C 5 , C 6  alkoxy, or 
       
       
         
           
           
               
               
           
         
         M is aryl, OH, C(O)NH 2 , COOH, SO 3 H, OSO 3 H, PO 3 H 2 , OPO 3 H 2 , NH 2 , NHR 19 , NR 19 R 20 , SO 2 R 21 , glycoside, lower C 1 , C 2 , C 3 , C 4 , C 5 , C 6  alkoxy, or 
       
       
         
           
           
               
               
           
         
         Q is aryl, OH, C(O)NH 2 , COOH, SO 3 H, OSO 3 H, PO 3 H 2 , OPO 3 H 2 , NH 2 , NHR 19 , NR 19 R 20 , SO 2 R 21 , glycoside, lower C 1 , C 2 , C 3 , C 4 , C 5 , C 6  alkoxy, or 
       
       
         
           
           
               
               
           
         
         R 19 , R 20  and R 21  are independently C 1 , C 2 , C 3 , C 4 , C 5 , or C 6  alkyl or R 19  and R 20  taken together with the attached nitrogen atom form a five membered ring; 
         V is a bond, —CH 2 —, —CH 2 CH 2 —, —CH 2 CH 2 CH 2 —, —O—CH 2 —, —OCH 2 CH 2 — or —OCH 2 CH 2 CH 2 —; 
         R 12 , R 13 , R 14 , R 15 , R 16 , Rn, and R 18 , are, independently, H or C 1 , C 2 , C 3 , C 4 , C 5 , or C 6  alkyl; and 
         Z is (CHR 1 ) n —C(O)—NR 2 (CHR 3 ) m —Ar, where Ar is a substituted or unsubstituted aryl or nitrogen-containing heteroaryl group, R 1 , R 2 , and R 3  are independently H or C 1 , C 2 , C 3 , C 4 , C 5 , or C 6  alkyl; and 
         n and m are, independently 0, 1, or 2; 
         provided that at least one of R a , R b , R c , R d , R e , R 4 , R 5 , and R 6  is P. 
       
     
     
         2 . A method of protecting against or treating hearing loss or osteoporosis in a subject comprising administering a compound having the Formula I: 
       
         
           
           
               
               
           
         
       
       or a salt, solvate, hydrate, or prodrug thereof, wherein:
 T is absent, CR 12 R 13 , C(O), O, S, S(O), S(O) 2 , NR 14 , C(R 15 R 16 )C(R 17 R 18 ), CH 2 O, or OCH 2 ; 
 X y  is CZ, CY, N, or N—O; 
 X z  is CZ, CY, N, or N—O; 
 at least one of X y  and X z  is CZ; 
 Y is selected from hydrogen, hydroxyl, halogen, lower (C 1 , C 2 , C 3 , C 4 , C 5 , or C 6 ) alkyl, C 1 , C 2 , C 3 , C 4 , C 5 , or C 6  alkoxy, O-lower (C 1 , C 2 , C 3 , C 4 , C 5 , or C 6 ) alkyl-aryl, and O-benzyl; 
 X a  is CR a  or N, or N—O; 
 X b  is CR b , N, or N—O; 
 X c  is CR c  or N, or N—O; 
 X d  is CR d  or N, or N—O; 
 X e  is CR e , N, or N—O; 
 R a , R b , R c , R d , R e , R 4 , R 5 , and R 6  are, independently, hydrogen, hydroxyl, halogen, P, C 1 , C 2 , C 3 , C 4 , C 5 , or C 6  alkyl, C 1 , C 2 , C 3 , C 4 , C 5 , or C 6  alkoxy, O-lower (C 1 , C 2 , C 3 , C 4 , C 5 , or C 6 ) alkyl-aryl, O-benzyl, C 1 , C 2 , C 3 , C 4 , C 5 , or C 6  alkyl-OH, COOH, COO-lower (C 1 , C 2 , C 3 , C 4 , C 5 , or C 6 ) alkyl, SO 2 H, SO 2 -lower (C 1 , C 2 , C 3 , C 4 , C 5 , or C 6 ) alkyl, 
 
       
         
           
           
               
               
           
         
       
       where W is H, or C 1 , C 2 , C 3 , C 4 , C 5 , or C 6  alkyl, C 1 , C 2 , C 3 , C 4 , C 5 , or C 6  alkyl-aryl;
 P is SO 3 H, OSO 3 H, OPO 3 H 2 , OPO 3 H 2 , NH 2 , NHR 19 , NHR 2 OR 21 , 
 
       
         
           
           
               
               
           
         
       
       tetrazole, O-lower (C 1 , C 2 , C 3 , C 4 , C 5 , or C 6 ) alkyl-K, O—C(O)-lower (C 1 , C 2 , C 3 , C 4 , C 5 , or C 6 ) alkyl-L, NH-lower (C 1 , C 2 , C 3 , C 4 , C 5 , or C 6 ) alkyl-M, or O-aryl-Q, further wherein lower alkyl is linear or branched alkyl;
 K is C(O)NH 2 , COOH, SO 3 H, OSO 3 H, PO 3 H 2 , OPO 3 H 2 , NH 2 , NHR 19 , NR 19 R 20 , SO 2 R 21 , glycoside, lower C 1 , C 2 , C 3 , C 4 , C 5 , C 6  alkoxy, or 
 
       
         
           
           
               
               
           
         
         L is aryl, OH, C(O)NH 2 , COOH, SO 3 H, OSO 3 H, PO 3 H 2 , OPO 3 H 2 , NH 2 , NHR 19 , NR 19 R 20 , SO 2 R 21 , glycoside, lower C 1 , C 2 , C 3 , C 4 , C 5 , C 6  alkoxy, or 
       
       
         
           
           
               
               
           
         
         M is aryl, OH, C(O)NH 2 , COOH, SO 3 H, OSO 3 H, PO 3 H 2 , OPO 3 H 2 , NH 2 , NHR 19 , NR 19 R 20 , SO 2 R 21 , glycoside, lower C 1 , C 2 , C 3 , C 4 , C 5 , C 6  alkoxy, or 
       
       
         
           
           
               
               
           
         
         Q is aryl, OH, C(O)NH 2 , COOH, SO 3 H, OSO 3 H, PO 3 H 2 , OPO 3 H 2 , NH 2 , NHR 19 , NR 19 R 20 , SO 2 R 29  glycoside, lower C 1 , C 2 , C 3 , C 4 , C 5 , C 6  alkoxy, or 
       
       
         
           
           
               
               
           
         
         R 19 , R 20  and R 21  are C 1 , C 2 , C 3 , C 4 , C 5 , or C 6  alkyl or R 19  and R 20  taken together with the attached nitrogen atom form a five membered ring; 
         V is a bond, —CH 2 —, —CH 2 CH 2 —, —CH 2 CH 2 CH 2 —, —O—CH 2 —, —OCH 2 CH 2 — or —OCH 2 CH 2 CH 2 —; 
         R 12 , R 13 , R 14 , R 15 , R 16 , R 17 , and R 18 , are, independently, H or C 1 , C 2 , C 3 , C 4 , C 5 , or C 6  alkyl; and 
         Z is (CHR 1 ) n —C(O)—NR 2 (CHR 3 ) m —Ar, where Ar is a substituted or unsubstituted aryl or nitrogen-containing heteroaryl group, R 1 , R 2 , and R 3  are independently H or C 1 , C 2 , C 3 , C 4 , C 5 , or C 6  alkyl; and 
         n and m are independently 0, 1, or 2. 
       
     
     
         3 . A method of preventing or treating a cell proliferation disorder comprising administering to a subject in need thereof a compound having the formula IA: 
       
         
           
           
               
               
           
         
       
       or a salt, solvate, hydrate, or prodrug thereof, wherein:
 T is absent, CR 12 R 13 , C(O), O, S, S(O), S(O) 2 , NR 14 , C(R 15 R 16 )C(R 17 R 18 ), CH 2 O, or OCH 2 ; 
 X y  is CZ, CY, N, or N—O; 
 X z  is CZ, CY, N, or N—O; 
 at least one of X y  and X z  is CZ; 
 Y is selected from hydrogen, hydroxyl, halogen, lower (C 1 , C 2 , C 3 , C 4 , C 5 , or C 6 ) alkyl, C 1 , C 2 , C 3 , C 4 , C 5 , or C 6  alkoxy, O-lower (C 1 , C 2 , C 3 , C 4 , C 5 , or C 6 ) alkyl-aryl, and O-benzyl; 
 X a  is CR a  or N, or N—O; 
 X b  is CR b , N, or N—O; 
 X c  is CR c  or N, or N—O; 
 X d  is CR d  or N, or N—O; 
 X e  is CR e , N, or N—O; 
 R a , R b , R c , R d , R e , R 4 , R 5 , and R 6  are, independently, hydrogen, hydroxyl, halogen, P, C 1 , C 2 , C 3 , C 4 , C 5 , or C 6  alkyl, C 1 , C 2 , C 3 , C 4 , C 5 , or C 6  alkoxy, O-lower (C 1 , C 2 , C 3 , C 4 , C 5 , or C 6 ) alkyl-aryl, O-benzyl, C 1 , C 2 , C 3 , C 4 , C 5 , or C 6  alkyl-OH, COOH, COO-lower (C 1 , C 2 , C 3 , C 4 , C 5 , or C 6 ) alkyl, SO 2 H, SO 2 -lower (C 1 , C 2 , C 3 , C 4 , C 5 , or C 6 ) alkyl, 
 
       
         
           
           
               
               
           
         
       
       wherein W is H, or C 1 , C 2 , C 3 , C 4 , C 5 , or C 6  alkyl, C 1 , C 2 , C 3 , C 4 , C 5 , or C 6  alkyl-aryl;
 P is SO 3 H, OSO 3 H, OPO 3 H 2 , OPO 3 H 2 , NH 2 , NHR 19 , NHR 2 OR 21 , 
 
       
         
           
           
               
               
           
         
       
       tetrazole, O-lower (C 1 , C 2 , C 3 , C 4 , C 5 , or C 6 ) alkyl-K, O—C(O)-lower (C 1 , C 2 , C 3 , C 4 , C 5 , or C 6 ) alkyl-L, NH-lower (C 1 , C 2 , C 3 , C 4 , C 5 , or C 6 ) alkyl-M, or O-aryl-Q, further wherein lower (C 1 , C 2 , C 3 , C 4 , C 5 , or C 6 ) alkyl is linear or branched alkyl;
 K is C(O)NH 2 , COOH, SO 3 H, OSO 3 H, PO 3 H 2 , OPO 3 H 2 , NH 2 , NHR 19 , NR 19 R 20 , SO 2 R 21 , glycoside, lower C 1 , C 2 , C 3 , C 4 , C 5 , C 6  alkoxy, or 
 
       
         
           
           
               
               
           
         
         L is aryl, OH, C(O)NH 2 , COOH, SO 3 H, OSO 3 H, PO 3 H 2 , OPO 3 H 2 , NH 2 , NHR 19 , NR 19 R 20 , SO 2 R 21 , glycoside, lower C 1 , C 2 , C 3 , C 4 , C 5 , C 6  alkoxy, or 
       
       
         
           
           
               
               
           
         
         M is aryl, OH, C(O)NH 2 , COOH, SO 3 H, OSO 3 H, PO 3 H 2 , OPO 3 H 2 , NH 2 , NHR 19 , NR 19 R 20 , SO 2 R 21 , glycoside, lower C 1 , C 2 , C 3 , C 4 , C 5 , C 6  alkoxy, or 
       
       
         
           
           
               
               
           
         
         Q is aryl, OH, C(O)NH 2 , COOH, SO 3 H, OSO 3 H, PO 3 H 2 , OPO 3 H 2 , NH 2 , NHR 19 , NR 19 R 20 , SO 2 R 21 , glycoside, lower C 1 , C 2 , C 3 , C 4 , C 5 , C 6  alkoxy, or 
       
       
         
           
           
               
               
           
         
         R 19 , R 20  and R 21  are independently C 1 , C 2 , C 3 , C 4 , C 5 , or C 6  alkyl or R 19  and R 20  taken together with the attached nitrogen atom form a five membered ring; 
         V is a bond, —CH 2 —, —CH 2 CH 2 —, —CH 2 CH 2 CH 2 —, —O—CH 2 —, —OCH 2 CH 2 — or —OCH 2 CH 2 CH 2 —; 
         R 12 , R 13 , R 14 , R 15 , R 16 , Rn, and R 18 , are, independently, H or C 1 , C 2 , C 3 , C 4 , C 5 , or C 6  alkyl; and 
         Z is (CHR 1 ) n —C(O)—NR 2 (CHR 3 ) m —Ar, where Ar is a substituted or unsubstituted aryl or nitrogen-containing heteroaryl group, R 1 , R 2 , and R 3  are independently H or C 1 , C 2 , C 3 , C 4 , C 5 , or C 6  alkyl; and n and m are, independently 0, 1, or 2; 
         provided that at least one of R a , R b , R c , R d , R e , R 4 , R 5 , and R 6  is P.

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