IP Library Granted Patent US 8,318,730
Granted Patent B2
US 8,318,730 · App. 12/380,007 · Granted Nov 27, 2012

Fused hetrocyclic compounds

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Quick Facts
Patent No.
US 8,318,730
App. No.
12/380,007
Granted
Nov 27, 2012
Kind
B2
Abstract

This invention provides fused heterocyclic compounds, pharmaceutical compositions of the compounds, and methods of using the compounds for the treatment of, inter alia, IL-12 related disease and disorders.

Claims (81)

1. A method for treating an interleukin-12 overproduction-related disorder, comprising administering to a subject in need thereof an effective amount of a compound of according to formula (V), or pharmaceutically acceptable salts thereof:

or a pharmaceutically acceptable salt thereof; wherein,

A 2 is —X—R′-L′-R″ and A 1 is a group represented by the following formula:

Ring D is a phenyl which may be further substituted with one or more substituents;

U and V are each, N;

Z is N;

W is O;

u is 0, 1, 2, 3, or 4;

X is O, S, S(O), S(O) 2 , N(R k ), C(O), C(S), C(S)NR k , C(NR), C(NR)NR k , C(O)NR k , C(O)NR k NR k , C(O)ONR k , C(O)NR k O, C(O)O, OC(O), OC(O)O, (C(R g )(R g )) m , (C(R g )(R g )) m NR k , (C(R g )(R g )) m O, (C(R g )(R g )) m S(O) p , (C(R g )(R g )) m N═C(R g ), C(R g )═N, C(R g )═N—O, C(R g )═N—S(O) p , C(R g )═N—NR k , C(R g )═N—C(CR g ) 2 , (C(R g )(R g )) m C(R g )═N, (C(R g )(R g )) m N═N, (C(R g )(R g )) m C(R g )═C(R g ), C(R g )═C(R g ), N═C(R g ), N(R k )N═C(R g ), N(R k )C(R g )═N, N(R k )C(R g )═C(R g ), N═N, N(R k )N═N, NR k C(O)NR k , NR k C(S)NR k , NR k C(O), NR k C(O)O, NR k C(NR)NR k , NR k C(S)O, NR k S(O) p NR k , OC(O)NR k , OC(S)NR k , OC(NR)NR k , OS(O) p NR k , C(NR)O, S(O) p NR k , or S(O) p NR k NR k ;

R, for each occurrence, is independently H, an optionally substituted alkyl, an optionally substituted cycloalkyl, an optionally substituted cyclyl, an optionally substituted aryl, an optionally substituted heterocycloalkyl, an optionally substituted heterocyclyl, an optionally substituted heteroaryl, an optionally substituted aralkyl, an optionally substituted heteroaralkyl, —C(O)R c , —OR k , —SR k , —NR h R j , hydroxylalkyl, nitro, cyano, haloalkyl, aminoalkyl, or —S(O) 2 R c ;

R′ is an optionally substituted cycloalkyl, an optionally substituted cyclyl, an optionally substituted heterocycloalkyl, an optionally substituted aryl, an optionally substituted heteroaryl, an optionally substituted aralkyl, an optionally substituted heteroaralkyl, or absent;

L′ is O, S, S(O), S(O) 2 , N(R k ), C(O), C(S), C(S)NR k , C(NR), C(NR)NR k , C(O)NR k , C(O)NR k NR k , C(O)ONR k , C(O)NR k O, C(O)O, OC(O), OC(O)O, (C(R g )(R g )) m , (C(R g )(R g )) m NR k , (C(R g )(R g )) m O, (C(R g )(R g )) m S(O) p , (C(R g )(R g )) m N═C(R g ), C(R g )═N, C(R g )═N—O, C(R g )═N—S(O) p , C(R g )═N—NR k , C(R g )═N—C(CR g ) 2 , (C(R g )(R g )) m C(R g )═N, (C(R g )(R g )) m N═N, (C(R g )(R g )) m C(R g )═C(R g ), C(R g )═C(R g ), N═C(R g ), N(R k )N═C(R g ), N(R k )C(R g )═N, N(R k )C(R g )═C(R g ), N═N, N(R k )N═N, NR k C(O)NR k , NR k C(S)NR k , NR k C(O), NR k C(O)O, NR k C(NR)NR k , NR k C(S)O, NR k S(O) p NR k , OC(O)NR k , OC(S)NR k , OC(NR)NR k , OS(O) p NR k , C(NR)O, S(O) p NR k , S(O) p NR k NR k or absent; and

R″ is H, an optionally substituted alkyl, an optionally substituted cycloalkyl, an optionally substituted cyclyl, an optionally substituted heterocycloalkyl, an optionally substituted heterocyclyl, an optionally substituted aryl, an optionally substituted heteroaryl, an optionally substituted aralkyl, an optionally substituted heteroaralkyl, N(R k )(CH 2 ) n R g , —OR k , —SR k , —NR h R j , hydroxylalkyl, —C(O)R c , —C(S)R c , —C(NR)R c , halo, haloalkyl, aminoalkyl, mercaptoalkyl, cyano, nitro, —S(O)R c , —S(O) 2 R c , —P(O)R c R c , —P(S)R c R c , or an optionally substituted alkylcarbonylalkyl;

Y is (CH(R g )) m , C(O), C(NR), O, S, S(O), S(O) 2 , N(R k ), or absent,

R 3 is R g , —C(O)R c , —OC(O)R c , —SC(O)R c , —NR k C(O)R c , —C(S)R c , —OC(S)R c , —SC(S)R c , —NR k C(S)R c , —C(NR)R c , —OC(NR)R c , —SC(NR)R c , —NR k C(NR)R c , —SO 2 R c , —S(O)R c , —NR k SO 2 R c , —OS(O) 2 R c , —OP(O)R c R c , or —P(O)R c R c ;

R 2 and R 4 are, independently for each occurrence, H, an optionally substituted alkyl, an optionally substituted alkylcarbonyl, —OR k , —SR k , —NR h R j , hydroxylalkyl, —C(O)R c , —OC(O)R c , —SC(O)R c , —NR k C(O)R c , —C(S)R c , —OC(S)R c , —SC(S)R c , —NR k C(S)R c , —C(NR)R c , —OC(NR)R c , —SC(NR)R c , —NR k C(NR)R c , —SO 2 R c , —S(O)R c , —NR k SO 2 R c , —OS(O) 2 R c , —OP(O)R c R c , —P(O)R c R c , halo, haloalkyl, aminoalkyl, mercaptoalkyl, cyano, nitro, nitroso, azide, an optionally substituted alkylcarbonylalkyl, an optionally substituted cyclyl, an optionally substituted cycloalkyl, an optionally substituted heterocyclyl, an optionally substituted heterocycloalkyl, an optionally substituted aryl, an optionally substituted aralkyl, an optionally substituted heteroaryl, an optionally substituted heteroaralkyl, or isothionitro; or R 2 and R 4 taken together are ═O, ═S, or ═NR;

R c , for each occurrence, is independently, H, an optionally substituted alkyl, an optionally substituted alkenyl, an optionally substituted alkynyl, an optionally substituted cyclyl, an optionally substituted cycloalkyl, an optionally substituted heterocyclyl, an optionally substituted heterocycloalkyl, an optionally substituted aralkyl, an optionally substituted heteroaralkyl, an optionally substituted aryl, an optionally substituted heteroaryl, haloalkyl, —OR k , —SR k , —NR h R j , hydroxylalkyl, alkylcarbonylalkyl, mercaptoalkyl, aminoalkyl, sulfonylalkyl, sulfonylaryl, or thioalkoxy;

R g , for each occurrence, is independently, H, an optionally substituted alkyl, an optionally substituted alkenyl, an optionally substituted alkynyl, an optionally substituted cyclyl, an optionally substituted cycloalkyl, an optionally substituted heterocyclyl, an optionally substituted heterocycloalkyl, an optionally substituted aralkyl, an optionally substituted heteroaralkyl, an optionally substituted aryl, an optionally substituted heteroaryl, haloalkyl, —OR k , —SR k , —NR h R j , hydroxylalkyl, alkylcarbonylalkyl, mercaptoalkyl, aminoalkyl, sulfonylalkyl, sulfonylaryl, thioalkoxy, —C(O)R c , —OC(O)R c , —SC(O)R c , —NR k C(O)R c , —C(S)R c , —OC(S)R c , —SC(S)R c , —NR k C(S)R c , —C(NR)R c , —OC(NR)R c , —SC(NR)R c , —NR k C(NR)R c , —SO 2 R c , —S(O)R c , —NR k SO 2 R c , —OS(O) 2 R c , —OP(O)R c R c , —P(O)R c R c , halo, aminoalkyl, mercaptoalkyl, cyano, nitro, nitroso, or azide;

R h and R j , for each occurrence, are independently H, an optionally substituted alkyl, an optionally substituted alkenyl, an optionally substituted alkynyl, an optionally substituted cyclyl, an optionally substituted cycloalkyl, an optionally substituted heterocyclyl, an optionally substituted heterocycloalkyl, an optionally substituted aralkyl, an optionally substituted heteroaralkyl, an optionally substituted aryl, an optionally substituted heteroaryl; or R h and R j taken together with the N to which they are attached is an optionally substituted heterocyclyl, an optionally substituted heterocycloalkyl, or an optionally substituted heteroaryl;

R k , for each occurrence, is independently H, an optionally substituted alkyl, an optionally substituted alkenyl, an optionally substituted alkynyl, an optionally substituted cyclyl, an optionally substituted cycloalkyl, an optionally substituted heterocyclyl, an optionally substituted heterocycloalkyl, an optionally substituted aralkyl, an optionally substituted heteroaralkyl, an optionally substituted aryl, an optionally substituted heteroaryl;

G is:

Hydrazide;

Hydrazone;

Hydrazine;

Hydroxylamine;

Oxime;

Amide;

Ester;

Carbonate;

Carbamate;

Thiocarbamate;

—NR k —C(NR)—NR k —;

—NR k —C(O)—NR k —;

—NR k —C(S)—NR k —;

—NR k —S(O) 2 —NR k —;

Phosphoryl;

an optionally substituted -Cyclyl-;

an optionally substituted -Heterocyclyl-;

an optionally substituted -Aryl-;

an optionally substituted -Heteroaryl-;

an optionally substituted -Heteroarylalkyl-;

an optionally substituted -Heteroaryl-NR k —;

an optionally substituted -Heteroaryl-S—;

an optionally substituted -Heteroarylalkyl-O—;

—Si(OR k ) 2 —;

—B(OR k )—

—C(NR)—NR k —;

—N(R k )—CRgR g —C(O)—;

—C(O)—ON(R k )—;

—C(O)—N(R k )O—;

—C(S)—ON(R k )—;

—C(S)—N(R k )O—;

—C(N(R k ))—ON(R k )—;

—C(N(R k ))—NR k O—;

—OS(O) 2 —N(R k )N(R k )—;

—OC(O)—N(R k )N(R k )—;

—OC(S)—N(R k )N(R k )—;

—OC(N(R k ))—N(R k )N(R k )—;

—N(R k )N(R k )S(O) 2 O—;

—N(R k )N(R k )C(S)O—;

—N(R k )N(R k )C(N(R k ))O—;

—OP(O)(R c )O—;

—N(R k )P(O)(R c )O—;

—OP(O)(R c )N(R k )—;

—N(R k )P(O)(R c )N(R k )—;

—P(O)(R c )O—;

—P(O)(R c )N(R k )—;

—N(R k )P(O)(R c )—;

—OP(O)(R c )—;

—O-alkyl-heterocyclyl-N(R k )—;

—N(R k )CHR g C(O)N(R k )CHR g C(O)—;

—N(R k )CHR g C(O)—;

—N(R k )C(O)CHR g —;

—C(O)N(R k )CHR g C(O)—;

or absent, each of which is optionally substituted;

m, for each occurrence, is independently 1, 2, 3, 4, 5, 6, 7, or 8;

n, for each occurrence, is independently 0, 1, 2, 3, 4, 5, 6, or 7;

p, for each occurrence, is independently 0, 1, or 2;

wherein, in formula (V), when G is absent, then R 3 is an optionally substituted alkyl, an optionally substituted aryl, an optionally substituted heteroaryl, an optionally substituted cycloalkyl, an optionally substituted cyclyl, an optionally substituted heterocycloalkyl, an optionally substituted heterocyclyl, nitro, cyano, halo, OR k , SR k , or NR h R j ; and

wherein the disorder is selected from the group consisting of multiple sclerosis, sepsis, myasthenia gravis, autoimmune neuropathies, Guillain-Barré syndrome, autoimmune uveitis, autoimmune hemolytic anemia, pernicious anemia, autoimmune thrombocytopenia, temporal arteritis, anti-phospholipid syndrome, vasculitides, Wegener's granulomatosis, Behcet's disease, psoriasis, psoriatic arthritis, dermatitis herpetiformis, pemphigus vulgaris, vitiligo, Crohn's disease, ulcerative colitis, interstitial pulmonary fibrosis, myelofibrosis, hepatic fibrosis, myocarditis, thyroditis, primary biliary cirrhosis, autoimmune hepatitis, immune-mediated diabetes mellitus, Grave's disease, Hashimoto's thyroiditis, autoimmune oophoritis and orchitis, autoimmune disease of the adrenal gland; rheumatoid arthritis, juvenile rheumatoid arthritis, systemic lupus erythematosus, scleroderma, polymyositis, dermatomyositis, spondyloarthropathies, ankylosing spondylitis, Sjogren's syndrome and graft-versus-host disease.

2. The method of claim 1 , wherein the disorder is rheumatoid arthritis, sepsis, Crohn's disease, multiple sclerosis, psoriasis, or immune-mediated diabetes mellitus.

Assignments (5)
SECURITY INTEREST Recorded Feb 18, 2026
From: ORPHAI THERAPEUTICS INC.
To: ACADIA WOODS PARTNERS, LLC, AS AGENT
Reel/Frame 074910/0274 →
SECURITY INTEREST Recorded Jul 17, 2025
From: MADRIGAL PHARMACEUTICALS, INC.
To: LSI FINANCING LLC, AS ADMINISTRATIVE AGENT
Reel/Frame 072038/0693 →
SECURITY INTEREST Recorded Jun 23, 2025
From: ORPHAI THERAPEUTICS INC.
To: ACADIA WOODS PARTNERS, LLC
Reel/Frame 071697/0788 →
CHANGE OF NAME Recorded May 3, 2021
From: SYNTA PHARMACEUTICALS CORP.
To: MADRIGAL PHARMACEUTICALS, INC.
Reel/Frame 056121/0785 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 17, 2009
From: ONO, MITSUNORI; SUN, LIJUN; WADA, YUMIKO; PRZEWLOKA, TERESA; LI, HAO; DEMKO, ZACHARY; CHIMMANAMADA, DINESH
To: SYNTA PHARMACEUTICALS CORPORATION
Reel/Frame 022855/0639 →