Substituted Pyrazoles as Modulators of Chemokine Receptors
Substituted pyrazole compounds such compounds represented by formula I: which are used to modulate the CCR-2 chemokine receptor to prevent or treat inflammatory and immunoregulatory disorders and diseases, allergic diseases, atopic conditions including allergic rhinitis, dermatitis, conjunctivitis, and asthma, as well as autoimmune pathologies such as rheumatoid arthritis and atherosclerosis; and pharmaceutical compositions comprising these compounds and the use of these compounds and compositions.
1 . A compound represented by Formula (I):
wherein:
R 1 and R 2 are each independently selected from —(C 0-6 alkyl)-W—(C 6-14 aryl), —(C 0-6 alkyl)-W-heterocycle and —(C 0-6 alkyl)-W—(C 3-7 cycloalkyl);
R 3 and R 4 are each independently selected from —C 0-6 alkyl, —(C 0-6 alkyl)-W—(C 1-6 alkyl), —(C 0-6 alkyl)-W—(C 3-7 cycloalkyl), —(C 0-6 alkyl)-W—(C 6-14 aryl), —(C 0-6 alkyl)-W-heterocycle, and —C(O)OR 6 ;
where each of R 1 , R 2 , R 3 and R 4 is independently unsubstituted or substituted with 1-7 substituents, where each of said 1-7 substituents is independently selected from halo, hydroxy, —O—C 1-3 alkyl, trifluoromethyl, —C 1-3 alkyl, —CO 2 R 6 , —CN, —N(R 6 ) 2 , —NR 6 COR 6 , —NRSO 2 R 6 , and —CONR 6 ;
R 5 is selected from hydrogen, —C 0-6 alkyl, —(C 0-6 alkyl)—(C 6-14 aryl), —(C 0-6 alkyl)-heterocycle, —(C 0-6 alkyl)-C 3-7 cycloalkyl and —(C 0-6 alkyl)-CO 2 R 6 ;
R 6 is independently selected from C 1-6 alkyl and NR 5 C(N)NH 2 , or two R 6 join to form a ring selected from pyrrolidinyl, piperidinyl and azepanyl;
X is CH 2 , N, O or S;
W is selected from a single bond, —O—, —S—, —SO—, —SO 2 —, —CO—, —CO 2 —, —CONR 6 — and —NR 6 —; and
n is 0-6;
or a pharmaceutically acceptable salt or an individual diastereomer thereof.
2 . The compound of claim 1 , wherein:
R 1 and R 2 are each independently selected from —(C 6-14 aryl) and —(C 6-14 heteroaryl);
R 3 and R 4 are each independently selected from —C 0-6 alkyl, —(C 0-6 alkyl)—(C 6-14 aryl), —(C 0-6 alkyl)-(C 6-14 heteroaryl),
where each of R 1 , R 2 , R 3 and R 4 is independently unsubstituted or substituted with 1-7 substituents, where each of said 1-7 substituents is independently selected from halo, hydroxy, —O—C 1-3 alkyl, trifluoromethyl, —C 1-3 alkyl, —CO 2 R 6 , —CN, —N(R 6 ) 2 , —NR 6 COR 6 , —NRSO 2 R 6 , and —CONR 6 ;
R 5 is —C 0-6 alkyl;
R 6 is independently selected from C 1-6 alkyl and NR 5 C(N)NH 2 , or two R 6 join to form a ring selected from pyrrolidinyl, piperidinyl and azepanyl;
X is CH 2 or O;
W is selected from a single bond, —O—, —S—, —SO—, —SO 2 —, —CO—, —CO 2 —, —CONR 6 — and —NR 6 —; and
n is 0-6;
or a pharmaceutically acceptable salt thereof, or an individual diastereomer thereof.
3 . A compound selected from the group consisting of:
or a pharmaceutically acceptable salt or individual diastereomer thereof.
4 . A pharmaceutical composition which comprises an inert carrier and the compound of claim 1 , or a pharmaceutically acceptable salt or individual diastereomer thereof.
5 . A method for modulation of chemokine receptor activity in a mammal which comprises the administration of an effective amount of the compound of claim 1 , or a pharmaceutically acceptable salt or individual diastereomer thereof.
6 . A method for treating, ameliorating, controlling or reducing the risk of an inflammatory or immunoregulatory disorder or disease which comprises the administration to a patient of an effective amount of the compound of claim 1 , or a pharmaceutically acceptable salt or individual diastereomer thereof.
7 . The method according to claim 6 , wherein said disorder or disease is selected from the group consisting of multiple sclerosis, rheumatoid arthritis, atherosclerosis, chronic obstructive pulmonary disease, obesity, type II diabetes and metabolic syndrome.