Cycloalkyl substituted pyrimidinediamine compounds and their uses
View Patent ↗The present disclosure provides 2,4-pyrimidinediamine compounds having antiproliferative activity, compositions comprising the compounds and methods of using the compounds to inhibit cellular proliferation and to treat proliferate diseases such as tumorigenic cancers.
1. A compound according to structural formula (I):
or an active salt or N-oxide thereof, wherein:
R 2 is an optionally substituted, heteroaryl, or heteroarylalkyl group;
R 4 is a saturated or unsaturated, bridged or unbridged cycloalkyl ring including an R 7 substituent, with the proviso that when the cycloalkyl ring is a saturated bridged cycloalkyl, or an unsaturated bridged or unbridged cycloalkyl, this R 7 substituent is optional;
R 5 is selected from hydrogen, an optionally substituted lower alkyl and a group selected from the group consisting of —CN, —NC, —NO 2 , halo, (C1-C3) haloalkyl, (C1-C3) perhaloalkyl, (C1-C3) fluoroalkyl, (C1-C3) perfluoroalkyl, —CF3, (C1-C3) haloalkoxy, (C1-C3) perhaloalkoxy, (C1-C3) fluoroalkoxy, (C1-C3) perfluoroalkoxy, —OCF 3 , OC(O)R a , —C(O)OR a , —C(O)CF 3 , and —C(O)CF 3 ;
R 7 is an amide or an ester group,
wherein each R a is independently selected from hydrogen, lower alkyl, lower cycloalkyl, (C6-C14) aryl, phenyl, naphthyl, (C7-C20) arylalkyl and benzyl.
2. The compound, active salt or N-oxide thereof of claim 1 in which R 5 is a group selected from the group consisting of —CN, —NC, —NO 2 , halo, (C1-C3) haloalkyl, (C1-C3) perhaloalkyl, (C1-C3) fluoroalkyl, (C1-C3) perfluoroalkyl, —CF3, (C1-C3) haloalkoxy, (C1-C3) perhaloalkoxy, (C1-C3) fluoroalkoxy, (C1-C3) perfluoroalkoxy, —OCF 3 , OC(O)R a , —C(O)OR a , —C(O)CF 3 , and —C(O)CF 3 .
3. The compound or active salt or N-oxide thereof of claim 2 in which R 5 is selected from nitro, cyano, halo, trifluoromethyl and trifluoromethoxy.
4. The compound, active salt or N-oxide of claim 1 in which R 2 is selected from
wherein:
Y 1 is selected from O, S, N, NH, N—(CH 2 ) y —R a , N—(CH 2 ) y —C(O)R a , N—(CH 2 ) y —C(O)OR a , N—(CH 2 ) y —S(O) 2 R a , N—(CH 2 ) y —S(O) 2 OR a and N—(CH 2 ) y —C(O)NR c R c ;
Y 2 is selected from O, S and S(O) 2 ;
R a is selected from hydrogen, lower alkyl, lower cycloalkyl, (C6-C14) aryl, phenyl, naphthyl, (C7-C20) arylalkyl and benzyl;
each R c is, independently of the other, an R a or, alternatively, two R c that are bonded to the same nitrogen atom may be taken together with this nitrogen atom to form a 5-8 membered heterocycloalkyl group which may optionally include from 1 to 3 additional heteroatomic groups selected from O, S, N—(CH 2 ) y —R a , N—(CH 2 ) y —C(O)R a , N—(CH 2 ) y —C(O)OR a , N—(CH 2 ) y —S(O) 2 R a , N—(CH 2 ) y —S(O) 2 OR a and N—(CH 2 ) y —C(O)NR a R a , and which may optionally include one or more of the same or lower alkyl substituents;
y is an integer ranging from 0 to 6; and
the bond including the dotted line may be a single bond or a double bond.
5. The compound, active salt or N-oxide of claim 1 in which R 4 is a substituted unbridged saturated cycloalkyl of the formula
where x is an integer ranging from 1 to 6 or a substituted unsaturated unbridged lower cycloalkyl selected from
6. The compound, active salt or N-oxide of claim 5 which is enriched in one or more of the (1S,2R), (1R,2S) and/or (1R,2R) diastereomer.
7. The compound, active salt or N-oxide of claim 5 which is enriched in the (1R,2S) diastereomer.
8. The compound, active salt or N-oxide of claim 5 which is substantially free of the (1S,2S) diastereomer.
9. The compound, active salt or N-oxide of claim 5 which is substantially pure in the (1R,2S) diastereomer.
10. The compound, active salt or N-oxide of claim 1 in which R 4 is an unsaturated unbridged lower cycloalkyl selected from
11. The compound, active salt or N-oxide of claim 10 which is enriched in one or more respective diastereomers selected from (1S,3S or 4S), (1S,3R or 4R), (1R,3S or 4S) and (1R,3R or 4R).
12. The compound, active salt or N-oxide of claim 10 which is enriched in the (1R,3S or 4S) diastereomer.
13. The compound, active salt or N-oxide of claim 10 which is substantially free of the (1S,3S or 4S) diastereomer.
14. The compound, active salt or N-oxide of claim 10 which is substantially pure in the (1R,3S or 4S) diastereomer.
15. The compound, active salt or N-oxide of claim 2 in which R 5 is selected from nitro, cyano or halo.
16. The compound, active salt or N-oxide of claim 2 in which R 5 is fluoro.
17. The compound, active salt or N-oxide of claim 1 in which the R 4 bridged or unbridged cycloalkyl ring is substituted with an R 7 substituent.
18. The compound, active salt or N-oxide of claim 17 , wherein R 7 is selected from —C(O)OR d and —C(O)NR d R d , in which
each R d is, independently of the others, selected from R a , R c and a chiral auxiliary group;
each R a is, independently of the others, selected from lower alkyl, lower cycloalkyl, (C6-C14) aryl, phenyl, naphthyl, (C7-C20) arylalkyl and benzyl;
each R c is, independently of the others, selected from R a or, alternatively, two R c that are bonded to the same nitrogen atom may be taken together with this nitrogen atom to form a 5-8 membered heterocycloalkyl group which may optionally include from 1 to 3 additional heteroatomic groups selected from O, S, N—(CH 2 ) y —R a , N—(CH 2 ) y —C(O)R a , N—(CH 2 ) y —C(O)OR a , N—(CH 2 ) y —S(O) 2 R a , N—(CH 2 ) y —S(O) 2 OR a and N—(CH 2 ) y —C(O)NR a R a , where y is an integer ranging from 0 to 6, and which may optionally include one or more of the same or different R 8 and/or lower alkyl substituents;
each R 8 group is, independently of the others, selected from R a , R b , lower cycloalkyl optionally substituted with one or more of the same or different R a and/or R b groups, lower heterocycloalkyl optionally substituted with one or more of the same or different R a and/or R b groups, lower alkoxy optionally substituted with one or more of the same or different R b groups and —O—(CH 2 ) x —R b , where x is an integer ranging from 1 to 6;
each R b is, independently of the others, selected from ═O, —OR a , (C1-C3) haloalkyloxy, —OCF 3 , ═S, —SR a , ═NR a , ═NOR a , —NR c R c halogen, —CF 3 , —CN, —NC, —OCN, —SCN, —NO, —NO 2 , ═N 2 , —N 3 , —S(O)R a , —S(O) 2 R a , —S(O) 2 OR a , —S(O)NR c R c , —S(O) 2 NR c R c , —OS(O)R a , —OS(O) 2 R a , —OS(O) 2 OR a , —OS(O) 2 NR c R c , —C(O)R a , —C(O)OR a , —C(O)NR c R c , —C(NH)NR c R c , —C(NR a )NR c R c , —C(NOH)R a , —C(NOH)NR c R c , —OC(O)R a , —OC(O)OR a , —OC(O)NR c R c , —OC(NH)NR c R c and —OC(NR a )NR c R c ; and
and each chiral auxiliary group is selected from
where R 9 is selected from hydrogen and lower alkyl.
19. The compound, active salt or N-oxide of claim 18 , wherein R 7 is selected from —C(O)NH 2 , —C(O)NH(lower alkyl), and —C(O)O(lower alkyl).
20. The compound, active salt or N-oxide of claim 18 , wherein R 7 is selected from —C(O)NH(chiral auxiliary) and —C(O)O(chiral auxiliary).