Classifications

• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
  • C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
  • C07D471/04—Ortho-condensed systems
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K31/00—Medicinal preparations containing organic active ingredients
  • A61K31/33—Heterocyclic compounds
  • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
  • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
  • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
  • A61K31/445—Non condensed piperidines, e.g. piperocaine
  • A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
  • A61K31/4545—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring hetero atom, e.g. pipamperone, anabasine
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K31/00—Medicinal preparations containing organic active ingredients
  • A61K31/33—Heterocyclic compounds
  • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
  • A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
  • A61K31/496—Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
  • A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
  • A61P1/18—Drugs for disorders of the alimentary tract or the digestive system for pancreatic disorders, e.g. pancreatic enzymes
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P11/00—Drugs for disorders of the respiratory system
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P13/00—Drugs for disorders of the urinary system
  • A61P13/12—Drugs for disorders of the urinary system of the kidneys
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D451/00—Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof
  • C07D451/02—Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof containing not further condensed 8-azabicyclo [3.2.1] octane or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane; Cyclic acetals thereof
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D451/00—Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof
  • C07D451/02—Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof containing not further condensed 8-azabicyclo [3.2.1] octane or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane; Cyclic acetals thereof
  • C07D451/04—Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof containing not further condensed 8-azabicyclo [3.2.1] octane or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane; Cyclic acetals thereof with hetero atoms directly attached in position 3 of the 8-azabicyclo [3.2.1] octane or in position 7 of the 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring system
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
  • C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
  • C07D471/08—Bridged systems
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
  • C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
  • C07D487/08—Bridged systems
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00

Definitions

• the present invention generally relates to substituted heteroaryl compounds useful as inhibitors of signaling through Toll-like receptor 9 (TLR9).
• TLR9 Toll-like receptor 9
• substituted heteroaryl compounds Provided herein are substituted heteroaryl compounds, compositions comprising such compounds, and methods of their use.
• the invention further pertains to pharmaceutical compositions containing at least one compound according to the invention that are useful for the treatment or prophylaxis of fibrotic diseases and other diseases, disorders, and conditions for which a TLR9 inhibitor is indicated.
• TLRs Toll-like receptors
• PAMPs pattern-associated molecular patterns
• MAMPs microbe-associated molecular patterns
• a total of 10 human TLRs have been identified and can be located in the cell surface or, as in the case of TLR7, 8 and 9, in the endolysosomes.
• TLR9 recognizes unmethylated single-stranded DNA containing cytosine-phosphate-guanine (CpG) motifs that are typically found in bacterial and mitochondrial DNA (mtDNA).
• CpG cytosine-phosphate-guanine
• TLR9 may contribute to fibrogenesis by promoting inflammation via the MyD88-dependent signalling pathway that ultimately mediates activation of IL-6, IFN-a, IL-ip, and TNF-a among others cytokines.
• TLR9 levels are higher in lung biopsies of rapid idiopathic pulmonary fibrosis (IPF) progressors than in the healthy or stable IPF progressors (Sci. Transl. Med. 2010, 2(57):57ra82).
• IPF idiopathic pulmonary fibrosis
• Circulating mtDNA the ligand for TLR9 has recently been identified as a mechanism-based prognostic biomarker of IPF (Am J. Resp. and Crit. Care Med. 2017, 196(12), 1502).
• TLR9 is up-regulated in human and murine non-alcoholic steatohepatitis (NASH) (Clin. Sci.
• TLR9 hepatocyte mitochondrial DNA drives NASH via activation of TLR9
• TLR9 inhibition has been recognized as a potential route to therapies for fibrotic diseases including idiopathic pulmonary fibrosis (Trujillo et al. Sci. Transl. Med. 2010, 2(57):57ra82; Yoshizaki et al. Ann Rheum Dis. 2016 Oct;75(10): 1858-65), non-alcoholic steatohepatitis (Garcia-Martinez et al. J Clin Invest 2016, 126: 859-864; Gabele et al. Biochem Biophys Res Commun. 2008; 376:271-276), hepatic injury (Shaker et al. Biochem Pharmacol. 2016. 112:90-101; Hoeque et al. J. Immun.
• TLR9 inhibitors Applicants have found potent compounds that have activity as TLR9 inhibitors. Further, applicants have found compounds that have activity as TLR9 inhibitors and are selective over TLR7 or TLR8. These compounds are provided to be useful as pharmaceuticals with desirable stability, bioavailability, therapeutic index, and toxicity values that are important to their drugability.
• the present invention relates to a new class of substituted heteroaryl compounds found to be effective inhibitors of signaling through TLR9. These compounds are provided to be useful as pharmaceuticals with desirable stability, bioavailability, therapeutic index, and toxicity values that are important to their drugability.
• the present invention provides compounds of Formula (I) that are useful as inhibitors of signaling through TLR9 and are useful for the treatment of fibrotic diseases, or stereoisomers, N-oxides, tautomers, pharmaceutically acceptable salts, solvates or prodrugs thereof.
• the present invention also provides pharmaceutical compositions comprising a pharmaceutically acceptable carrier and at least one of the compounds of the present invention or stereoisomers, tautomers, pharmaceutically acceptable salts, solvates, or prodrugs thereof.
• the present invention also provides a method for inhibition of Toll-like receptor 9 comprising administering to a host in need of such treatment a therapeutically effective amount of at least one of the compounds of the present invention or stereoisomers, tautomers, pharmaceutically acceptable salts, solvates, or prodrugs thereof.
• the present invention also provides a method for treating fibrotic diseases, comprising administering to a host in need of such treatment a therapeutically effective amount of at least one of the compounds of the present invention or stereoisomers, tautomers, pharmaceutically acceptable salts, solvates, or prodrugs thereof.
• the present invention also provides a method of treating a disease or disorder associated with TLR9 activity, the method comprising administering to a mammal in need thereof, at least one of the compounds of Formula (I) or salts, solvates, and prodrugs thereof.
• the present invention also provides processes and intermediates for making the compounds of Formula (I) including salts, solvates, and prodrugs thereof.
• the present invention also provides at least one of the compounds of Formula (I) or salts, solvates, and prodrugs thereof, for use in therapy.
• the present invention also provides the use of at least one of the compounds of Formula (I) or salts, solvates, and prodrugs thereof, for the manufacture of a medicament for the treatment of prophylaxis of TLR9 related conditions, such as fibrotic diseases, allergic diseases, autoimmune diseases, and inflammatory diseases.
• compositions comprising the compounds of Formula (I) may be used in treating, preventing, or curing various TLR9 related conditions.
• Pharmaceutical compositions comprising these compounds are useful for treating, preventing, or slowing the progression of diseases or disorders in a variety of therapeutic areas, such as fibrotic diseases, allergic diseases, autoimmune diseases, and inflammatory diseases.
• the first aspect of the present invention provides at least one compound of Formula (I): or stereoisomers, tautomer, solvates or salts thereof, wherein: one of X and Y is N and the other of X and Y is C-A; one of Qi and Q2 is G and the other Qi and Q2 is R3;
• A is piperidinyl, phenyl, pyridinyl, pyrimidinyl, 6-azabicyclo[3.2.1]octanyl, or azabicyclo[3.2.1]octanyl, each substituted with -L-R.4 and zero to 2 R4b;
• L is a bond, -CRxRx-, or -C(0)(CR x Rx)o-2-;
• Ri is hydrogen, C1-3 alkyl, C1-2 fluoroalkyl, or C3-4 cycloalkyl; each R2 is independently halo, -CN, -OH, -NO2, Ci-4 alkyl, C1-2 fluoroalkyl, C1-2 cyanoalkyl, C1-3 hydroxyalkyl, C1-3 aminoalkyl, -O(CH2)I-2OH, -(CH2)o-40(Ci-4 alkyl), C1-3 fluoroalkoxy, -(CH 2 )I- 4 O(CI-3 alkyl), -O(CH 2 )I- 2 OC(O)(CI-3 alkyl), -O(CH 2 )I- 2 NRXRX, -C(O)O(CI-3 alkyl), -(CH 2 )o-2C(0)NR y Ry, -C(O)NR X (CI- 5 hydroxyalkyl), -C(O)NR x (C2-6 alkoxyalkyl), -C
• R 2a is C1-6 alkyl, C1-3 fluoroalkyl, C1-6 hydroxyalkyl, C1-3 aminoalkyl, -(CH2)o-40(Ci-3 alkyl), C3-6 cycloalkyl, -(CH2)I-3C(O)NR X RX, -CH2(C3-6 cycloalkyl), -CH2(phenyl), tetrahydrofuranyl, tetrahydropyranyl, or phenyl; each R2b is independently H, halo, -CN, -NRxRx, C1-6 alkyl, C1-3 fluoroalkyl, C1-3 hydroxyalkyl, C1-3 fluoroalkoxy, -(CH2)O-20(CI-3 alkyl), -(CH2)o-3C(0)NR x Rx, -(CH 2 )I-3(C3-6 cycloalkyl), -C(O)O(Ci-3 alkyl), -C(O)NR X (CI-3
• R2C is R 2a or R2b;
• R2d is R 2a or R2b; provided that one of R2c and R2d is R2a, and the other of R2c and R2d is R2b;
• R3 is hydrogen, F, C1-3 alkyl, or C3-4 cycloalkyl;
• R4 is:
• each R4a is independently -OH, C1-6 alkyl, C1-3 fluoroalkyl, C3-6 cycloalkyl, -CH 2 (C3-6 cycloalkyl), -C(O)(Ci-4 alkyl), -C(O)(C3-6 cycloalkyl), -C(O)(phenyl), -C(O)CH 2 (C 3 -6 cycloalkyl), -C(O)CH 2 (phenyl), or -C(O)O(Ci-4 al
• the second aspect of the present invention provides at least one compound of Formula (I): or a salt thereof, wherein: one of X and Y is N and the other of X and Y is C-A; one of Qi and Q 2 is G and the other Qi and Q 2 is R 3 ; G is:
• A is piperidinyl, phenyl, pyridinyl, pyrimidinyl, 6-azabicyclo[3.2.1]octanyl, or azabicyclo[3.2.1]octanyl, each substituted with -L-R.4 and zero to 1 R4b;
• L is a bond, -CRxRx- or -C(0)(CR x Rx)o-2-;
• Ri is hydrogen, C1-3 alkyl, C1-2 fluoroalkyl, or C3-4 cycloalkyl; each R2 is independently halo, -CN, -OH, -NO2, Ci-4 alkyl, C1-2 fluoroalkyl, C1-2 cyanoalkyl, C1-3 hydroxyalkyl, C1-3 aminoalkyl, -O(CH2)I-2OH, -(CH2)O-40(CI-4 alkyl), C1-3 fluoroalkoxy, -(CH 2 )I-4O(CI-3 alkyl), -O(CH 2 )I- 2 OC(O)(CI-3 alkyl), -O(CH 2 )I- 2 NRXRX, -C(O)O(CI-3 alkyl), -(CH 2 )o-2C(0)NR y Ry, -C(O)NR X (CI- 5
• R 2a is C1-6 alkyl, C1-3 fluoroalkyl, C1-6 hydroxyalkyl, C1-3 aminoalkyl, -(CH 2 )O-40(CI-3 alkyl), C3-6 cycloalkyl, -(CH 2 )I-3C(O)NR X RX, -CH 2 (C3-6 cycloalkyl), -CH 2 (phenyl), tetrahydrofuranyl, tetrahydropyranyl, or phenyl; each R 2 b is independently H, halo, -CN, -NRxRx, C1-6 alkyl, C1-3 fluoroalkyl, C1-3 hydroxyalkyl, C1-3 fluoroalkoxy, -(CH 2 )O- 2 0(CI-3 alkyl), -(CH 2 )o-3C(0)NR x Rx, -(CH 2 )I- 3 (C3-6 cycloalkyl), -C(O)O(Ci-3 alkyl),
• R 2C is R 2a or R 2 b;
• RM is R 2a or RM; provided that one of RM and R is R 2a , and the other of R and RM is R ;
• R3 is hydrogen, C1-3 alkyl, or C3-4 cycloalkyl
• R4 is:
• each R4a is independently Ci-6 alkyl, C1-3 fluoroalkyl, C3-6 cycloalkyl, -CH2(C3-6 cycloalkyl), -C(O)(Ci-4 alkyl), -C(O)(C3-6 cycloalkyl), -C(O)(phenyl), -C(O)CH 2 (C3-6 cycloalkyl), -C(O)CH 2 (phenyl), or -C(O)O(Ci-4 alkyl);
• R 4 b is F, Cl, or -CH3; each R4C is independently C1-6 alkyl, C1-3 fluoroalkyl, -CH 2 (C3-6 cycloalkyl), -C(O)(Ci-4 alkyl), -C(O)(phenyl), -C(O)CH 2 (phenyl), -C(O)OCH 2 CH 3 , or C3-6 cycloalkyl; each Rs is independently hydrogen, F, Cl, C1-2 alkyl, or cyclopropyl; each R x is independently H or -CH3; each R y is independently H or C1-6 alkyl; m is zero, 1, or 2; n is zero, 1, or 2; and p is zero, 1, 2, 3, or 4.
• a compound of Formula (I) or stereoisomers, tautomer, solvates or salts thereof is provided wherein X is C-A and Y is N.
• Compounds of this embodiment have the structure of Formula (II):
• a compound of Formula (I) or stereoisomers, tautomer, solvates or salts thereof wherein X is C-A and Y is N; and Qi is G and Q2 is R3.
• Compounds of this embodiment have the structure of Formula (Ila):
• a compound of Formula (I) or stereoisomers, tautomer, solvates or salts thereof wherein X is C-A and Y is N; and Qi is R3 and Q2 is G.
• Compounds of this embodiment have the structure of Formula (lib) :
• a compound of Formula (I) or stereoisomers, tautomer, solvates or salts thereof is provided wherein X is N and Y is C-A.
• Compounds of this embodiment have the structure of Formula (III):
• a compound of Formula (I) or stereoisomers, tautomer, solvates or salts thereof wherein X is N and Y is C-A; and Qi is G and Q2 is R3.
• Compounds of this embodiment have the structure of Formula (Illa):
• a compound of Formula (I) or stereoisomers, tautomer, solvates or salts thereof wherein X is N and Y is C-A; and Qi is R3 and Q2 is G.
• Compounds of this embodiment have the structure of Formula (Illb):
• a compound of Formula (I) or stereoisomers, tautomer, solvates or salts thereof is provided wherein G is phenyl substituted with 1 to 3 substituents independently selected from -OCH3, -S(O)2CH3, -S(O)2N(CH3)2,
• G is phenyl substituted with 1 to 2 substituents independently selected from -OCH3, -S(O)2CH3, -S(O)2N(CH3)2, and -S(O)2(cyclopropyl). Also included in this embodiment are compounds in which G is:
• a compound of Formula (I) or stereoisomers, tautomer, solvates or salts thereof is provided wherein G is phenyl substituted with 1 to 2 substituents independently selected from -OCH3, -S(O)2CH3, -S(O)2N(CH3)2, and
• G is phenyl substituted with 1 to 2 substituents independently selected from -OCH3 and -S(O)2CH3.
• a compound of Formula (I) or stereoisomers, tautomer, solvates or salts thereof is provided wherein G is .
• each R2 is independently F, Cl, Br, -CN, -OH, -CH3, -CH2CH3, -CF3, -CH2OH, -C(CH 3 )2OH, -CH2NH2, -0CH3, -OCH2CH3, -OCH(CH 3 )2, -OCH2CH2OCH3, -OCH 2 CH 2 N(CH3)2, -OCHF2, -C(O)OCH3, -C(O)NH 2 , -C(O)NH(CH 2 CH 3 ), -C(O)(thiazolyl), -NH2, -NH(CH 3 ), -NH(CH 2 CH 3 ), -N(CH 3 ) 2 , -NHC(O)CH 3 , -NHC(O)C(CH 3 )3,
• each R2 is independently F, Cl, -CN, -CH3, -OCH3, -NH2, or cyclopropyl.
• p is 2; one R2 is -CH3; and the other R2 is F, Cl, -CN, -CH3, -OCH3, -NH2, or cyclopropyl.
• a compound of Formula (I) or stereoisomers, tautomer, solvates or salts thereof is provided wherein G is a 9-membered heterocyclic ring selected from:
• a compound of Formula (I) or stereoisomers, tautomer, solvates or salts thereof is provided wherein G is a 10-membered heterocyclic ring selected from:
• each R 2 is independently Cl, -CH 3 , -CH2CH3, -CH2OH, -CH2CH2OH, -CH2CN, -OCH3, -CH2OCH3, or -CH 2 CH 2 S(O)2CH3.
• each R2 is independently Cl, -CH3, -CH2CH3, -CH2OH, -CH2CH2OH, -CH2CN, -OCH3, -CH2OCH3, or -CH 2 CH 2 S(O)2CH3.
• a compound of Formula (I) or stereoisomers, tautomer, solvates or salts thereof is provided wherein p is zero, 1, 2, or 3. Included in this embodiment are compounds in which p is 1 or 2.
• a compound of Formula (I) or stereoisomers, tautomer, solvates or salts thereof is provided wherein A is piperidinyl, phenyl, pyridinyl, pyrimidinyl, 6-azabicyclo[3.2.1]octanyl, or azabicyclo[3.2.1]octanyl, each substituted with -L-R4 and zero to 2 R4b.
• a compound of Formula (I) or stereoisomers, tautomer, solvates or salts thereof wherein A is piperidinyl, phenyl, pyridinyl, pyrimidinyl, 6-azabicyclo[3.2.1]octanyl, or azabicyclo[3.2.1]octanyl, each substituted with -L-R4 and zero to 1 R4b.
• a compound of Formula (I) or stereoisomers, tautomer, solvates or salts thereof is provided wherein A is piperidinyl, phenyl, or pyridinyl, each substituted with -L-R.4 and zero to 2 R4b.
• A is piperidinyl or phenyl, each substituted with -L-R.4 and zero to 1 R.4b. Also, included in this embodiment are compounds in which A is phenyl or pyridinyl, each substituted with -L-R and zero to 1 R4b.
• a compound of Formula (I) or stereoisomers, tautomer, solvates or salts thereof is provided wherein A is piperidinyl, phenyl, or pyridinyl, each substituted with -L-R4 and zero to 1 R4b. Included in this embodiment are compounds in which A is piperidinyl or phenyl, each substituted with -L-R4 and zero to 1 R4b. Also, included in this embodiment are compounds in which A is phenyl or pyridinyl, each substituted with -L-R4 and zero to 1 R4b.
• a compound of Formula (I) or stereoisomers, tautomer, solvates or salts thereof wherein A is piperidinyl, phenyl, pyridinyl, or pyrimidinyl, each substituted with -L-R4 and zero to 2 R4b; and L is a bond. Included in this embodiment are compounds in which A is piperidinyl, phenyl, or pyridinyl, each substituted with -L-R4 and zero to 1 R4b; and L is a bond.
• a compound of Formula (I) or stereoisomers, tautomer, solvates or salts thereof wherein A is piperidinyl, phenyl, pyridinyl, or pyrimidinyl, each substituted with -L-R4 and zero to 1 R4b; and L is a bond. Included in this embodiment are compounds in which A is piperidinyl, phenyl, or pyridinyl, each substituted with -L-R4 and zero to 1 R4b; and L is a bond.
• a compound of Formula (I) or stereoisomers, tautomer, solvates or salts thereof is provided wherein L is a bond.
• a compound of Formula (I) or stereoisomers, tautomer, solvates or salts thereof is provided wherein L is -CRxRx- Included in this embodiment are compounds in which L is -CH2-.
• a compound of Formula (I) or stereoisomers, tautomer, solvates or salts thereof is provided wherein L is -C(0)(CR x Rx)o-2-. Included in this embodiment are compounds in which L is -C(0)(CH2)o-2- Also included in this embodiment are compounds in which L is -C(0)(CH2)O-I- Additionally, included in this embodiment are compounds in which L is -C(O)-.
• a compound of Formula (I) or stereoisomers, tautomer, solvates or salts thereof is provided wherein L is -CRxRx- or -C(0)(CR x Rx)o-2-. Included in this embodiment are compounds in which L is -CRxRx- or -C(0)(CR x Rx)o- i-. Also included in this embodiment are compounds in which L is -CRxRx- or -C(O)-. Additionally, included in this embodiment are compounds in which each R x is hydrogen.
• a compound of Formula (I) or stereoisomers, tautomer, solvates or salts thereof is provided wherein L is a bond, -CH2- or -C(0)(CH2)o-2- Included in this embodiment are compounds in which L is a bond or -C(O)-.
• a compound of Formula (I) or stereoisomers, tautomer, solvates or salts thereof is provided wherein R4 is -N(CH3)2.
• a compound of Formula (I) or stereoisomers, tautomer, solvates or salts thereof wherein R4 is morpholinyl, pyrrolidinyl, piperidinyl, piperazinyl, pyridinyl, dioxothiomorpholinyl, azaspiro[3.3]heptanyl, azabicyclo[3.2.1]octanyl, diazabicyclo[2.2.2]octanyl, or diazabicyclo[3.2.1]octanyl, each substituted with zero to 4 R4a.
• a compound of Formula (I) or stereoisomers, tautomer, solvates or salts thereof wherein R4 is morpholinyl, pyrrolidinyl, piperidinyl, piperazinyl, pyridinyl, dioxothiomorpholinyl, azabicyclo[3.2.1]octanyl, diazabicyclo[2.2.2]octanyl, or diazabicyclo[3.2.1]octanyl, each substituted with zero to 4 R4a.
• a compound of Formula (I) or stereoisomers, tautomer, solvates or salts thereof is provided wherein R4 is pyrrolidinyl, piperidinyl, piperazinyl, or pyridinyl, each substituted with zero to 4 R4a.
• a compound of Formula (I) or stereoisomers, tautomer, solvates or salts thereof is provided wherein R4 is pyrrolidinyl, piperidinyl, piperazinyl, pyridinyl, azaspiro[3.3]heptanyl, or azabicyclo[3.2.1]octanyl, each substituted with zero tO 2 R4a.
• a compound of Formula (I) or stereoisomers, tautomer, solvates or salts thereof is provided wherein R4 is pyrrolidinyl, piperidinyl, piperazinyl, or pyridinyl, each substituted with zero to 2 R4a. Included in this embodiment are compounds in which R4 is pipendinyl, piperazinyl, or pyndinyl. Also included in this embodiment are compounds in which R4 is piperidinyl or piperazinyl.
• a compound of Formula (I) or stereoisomers, tautomer, solvates or salts thereof is provided wherein Included in this embodiment are compounds in which n is 1 or 2. Also included in this embodiment are compounds in which n is 1. Additionally, included in this embodiment are compounds in which n is 2.
• a compound of Formula (I) or stereoisomers, tautomer, solvates or salts thereof wherein R4 is pyrrolidinyl, piperidinyl, piperazinyl, or (R-lclm -N N- ⁇ pyridinyl, each substituted with zero to 2 R4 a ; or r ' n
• a compound of Formula (I) or stereoisomers, tautomer, solvates or salts thereof is provided wherein R4 is pyrrolidinyl, piperidinyl, piperazinyl, or pyridinyl, each substituted with zero t
• R4 is pyrrolidinyl, piperidinyl, piperazinyl, or pyridinyl, each substituted with zero to 2 R4 a ; or
• each R4 a is independently -OH, C1-6 alkyl
• each R4 a is independently -OH, C1-6 alkyl, C1-3 fluoroalkyl, -CH2(C3-6 cycloalkyl), -C(O)(Ci-4 alkyl), -C(O)(phenyl), -C(O)CH 2 (phenyl), -C(O)OCH 2 CH 3 , or C3-6 cycloalkyl.
• each R4a is independently -OH, -CH3, -CHCH3, -CH(CH 3 ) 2 , -CH 2 CH(CH 3 ) 2 , -C(CH 3 )3, -CH 2 C(CH 3 )3, -CH 2 CH 2 C(CH 3 )3, -CF3, -CH 2 CH 2 OH, -CH 2 CH 2 CH 2 OH, -CH 2 C(CH 3 ) 2 OH, -CH 2 CH 2 C(CH 3 ) 2 OH, -CH 2 CH 2 OCH 3 , -CH 2 (cyclopropyl), -C(O)CH 3 , -C(O)CH(CH 3 ) 2 , -C(O)CH 2 CH 3 , -C(O)(phenyl), -C(O)CH 2 (phenyl), -C(O)OCH
• each R4a is independently -OH, -CH3, -CHCH3, -CH(CH 3 ) 2 , -CH 2 CH(CH 3 ) 2 , -C(CH 3 )3, -CF 3 , -CH 2 CH 2 OH, -CH 2 CH 2 CH 2 OH, -CH 2 C(CH 3 ) 2 OH, -CH 2 CH 2 C(CH 3 ) 2 OH, -CH 2 CH 2 OCH 3 , -CH 2 (cyclopropyl), -C(O)CH3, -C(O)(phenyl), -C(O)OCH 2 CH3, cyclopropyl, cyclobutyl, oxetanyl, tetrahydrofuranyl, tetrahydropyranyl, -(CH 2 )i- 2 (bromophenyl), or
• each R4b is independently F or -CH3. Included in this embodiment are compounds in which each R4b is -CH3.
• a compound of Formula (I) or stereoisomers, tautomer, solvates or salts thereof is provided wherein R4b is F or Cl. Included in this embodiment are compounds in which R4b is F.
• a compound of Formula (I) or stereoisomers, tautomer, solvates or salts thereof is provided wherein A is phenyl substituted with -L-R4 and zero to 2 R4b. Included in this embodiment are compounds in which each R4b is F.
• each R4c is independently Ci-4 alkyl, C1-2 fluoroalkyl, -CH 2 (C 3 -6 cycloalkyl), -C(O)(Ci-3 alkyl), -C(O)(phenyl), -C(O)CH 2 (phenyl), -C(O)OCH 2 CH3, or C3-6 cycloalkyl.
• each R4c is independently C1-3 alkyl, Ci- 2 fluoroalkyl, -CH 2 (C 3 -4 cycloalkyl), -C(O)(Ci-2 alkyl), -C(O)(phenyl), -C(O)CH 2 (phenyl), -C(O)OCH 2 CH 3 , or C3-4 cycloalkyl.
• a compound of Formula (I) or stereoisomers, tautomer, solvates or salts thereof is provided wherein Ri is hydrogen, Ci- 2 alkyl, -CH 2 F, -CHF 2 , -CF3, or C3-4 cycloalkyl. Included in this embodiment are compounds in which Ri is hydrogen, -CH3, -CF3, or cyclopropyl. Also included in this embodiment are compounds in which Ri is hydrogen or -CH3.
• a compound of Formula (I) or stereoisomers, tautomer, solvates or salts thereof is provided wherein Ri is hydrogen, Ci- 2 alkyl, -CH 2 F, -CHF 2 , -CF3, or cyclopropyl. Included in this embodiment are compounds in which Ri is hydrogen, -CH3, -CHF 2 , or cyclopropyl. Also included in this embodiment are compounds in which Ri is hydrogen. Also included in this embodiment are compounds in which Ri is -CH3, -CHF 2 , or cyclopropyl.
• each R 2 is independently F, Cl, -CN, -OH, C1-3 alkyl, Ci- 2 fluoroalkyl, Ci- 2 cyanoalkyl, C1-3 hydroxyalkyl, Ci- 2 aminoalkyl, -(CH 2 )O- 2 0(CI-3 alkyl), C3-6 cycloalkyl, -NRxRx, -(CH 2 )o- 2 C(0)NR x Rx, -CH 2 (C 3 -6 cycloalkyl), -CH 2 (phenyl), or phenyl.
• each R 2 is independently Cl, -CH3, -CH 2 CH 3 , -CH 2 OH, -CH 2 CH 2 OH, -CH 2 CN, -OCH3, -CH 2 OCH3, or -CH 2 CH 2 S(O) 2 CH3. Also, included in this embodiment are compounds in which each R 2 is independently Cl, -CH3, -CH 2 OH, or -OCH3.
• R 2a is Ci-4 alkyl, C1-2 fluoroalkyl, Ci-4 hydroxyalkyl, -(CH 2 )i-3OCH3, C3-6 cycloalkyl, -CH 2 C(O)NR x Rx, -CH 2 (C 3 -6 cycloalkyl), -CH 2 (phenyl), tetrahydrofuranyl, or phenyl; and each R 2 b is independently H, F, Cl, -CN, -NRxRx, Ci-6 alkyl, C1-2 fluoroalkyl, C1-3 hydroxyalkyl, -(CH 2 )o- 2 0(Ci- 2 alkyl), -(CH 2 )O- 2 C(0)NRXRX, -(CH 2 )i-3(cyclopropyl), -C(O)O(Ci- 2 alkyl),
• R 2a is -CH3; and each R 2 b is independently H, Cl, or -CH3.
• R3 is hydrogen, F, C1-3 alkyl, or C3-4 cycloalkyl.
• R3 is hydrogen, F, C1-2 alkyl, or cyclopropyl.
• R3 is hydrogen, F, -CH3, or cyclopropyl.
• a compound of Formula (I) or stereoisomers, tautomer, solvates or salts thereof is provided wherein R3 is hydrogen, C1-2 alkyl, or C3-4 cycloalkyl. Included in this embodiment are compounds in which R3 is hydrogen, C1-2 alkyl, or cyclopropyl. Also included in this embodiment are compounds in which R3 is hydrogen or -CH3.
• each Rs is independently hydrogen, F, Cl, Ci- 3 alkyl, C1-3 hydroxyalkyl, C1-2 alkoxy, cyclopropyl, or morpholinyl. Included in this embodiment are compounds in which each Rs is independently hydrogen, -CH3, -C(CH3)2OH, -OCH3, or morpholinyl.
• each Rs is independently hydrogen, F, Cl, -CH3, or cyclopropyl. Included in this embodiment are compounds in which each Rs is independently hydrogen, -CH3, or cyclopropyl. Also included are compounds in which each Rs is hydrogen or -CH3.
• G is phenyl substituted with 1 to 2 substituents independently selected from -OCH3, -S(O)2CH3, -S(O)2N(CH3)2, and -S(O)2(cyclopropyl);
• A is piperidinyl, phenyl, or pyridinyl, each substituted with -L-R4 and zero to 2 R4b;
• L is a bond, -CH2-, -C(O)-, -C(O)CH2- or -C(O)CH2CH2-;
• Ri is hydrogen, -CH3, -CHF2, or cyclopropyl;
• R3 is hydrogen, F, -CH3, or cyclopropyl;
• R4 is: (i) -N(CH3)2; or (ii) pyrrolidinyl, piperidinyl, piperazinyl, or pyr
• G is phenyl substituted with 1 to 2 substituents independently selected from -OCH3, -S(O)2CH3, -S(O)2N(CH3)2, and -S(O)2(cyclopropyl);
• A is piperidinyl, phenyl, or pyridinyl, each substituted with -L-R4 and zero to 2 R4t>;
• L is a bond, -CH2-, -C(O)-, -C(O)CH2- or -C(O)CH2CH2-;
• Ri is hydrogen or -CH3;
• R3 is hydrogen, F, -CH3, or cyclopropyl;
• R4 is: (i) -N(CH3)2; or (ii) pyrrolidinyl, piperidinyl, piperazinyl, or pyridinyl, each substituted with zero to
• A is piperidinyl, phenyl, pyridinyl, or pyrimidinyl, each substituted with -L-R.4 and zero to 1 R4b;
• L is a bond, -CRxRx- or -C(0)(CR x Rx)o-2-;
• Ri is hydrogen, C1-3 alkyl, C1-2 fluoroalkyl, or C3-4 cycloalkyl; each R2 is independently F, Cl, -CN, -OH, C1-3 alkyl, C1-2 fluoroalkyl, C1-2 cyanoalkyl, C1-3 hydroxyalkyl, C1-2 aminoalkyl, -(CH2)O-20(CI-3 alkyl), C3-6 cycloalkyl, -NRxRx, -(CH 2 )O- 2 C(0)NRXRX, -CH2(C3-6 cycloalkyl), -CH2(phenyl), or phenyl;
• R3 is hydrogen, C1-3 alkyl, or C3-4 cycloalkyl
• R4 is:
• each R4a is independently C1-6 alkyl, C1-3 fluoroalkyl, C3-6 cycloalkyl, -CH2(C3-6 cycloalkyl), -C(O)(Ci-4 alkyl), -C(O)(C3-6 cycloalkyl), -C(O)(phenyl), -C(O)CH 2 (C3-6 cycloalkyl), -C(O)CH 2 (phenyl), or -C(O)O(Ci-4 alkyl);
• G is phenyl substituted with 1 to 2 substituents independently selected from -OCH 3 and -S(O) 2 CH 3 ;
• A is piperidinyl, phenyl, or pyridinyl, each substituted with -L-R4 and zero to 1 R4b;
• L is a bond, -CH 2 - — C(O)— , -C(O)CH 2 -, or -C(O)CH 2 CH 2 -;
• RI is hydrogen or -CH 3 ;
• R 3 is hydrogen or -CH 3 ;
• R4 is: (i) -N(CH 3 ) 2 ; or (ii) pyrrolidinyl, piperidinyl, piperazinyl, or pyridinyl, each substituted with zero to 2 R4 a ;
• R4a is independently C1-6 alkyl, Ci- 3
• G is phenyl substituted with 1 to 2 substituents independently selected from -OCH 3 and -S(O) 2 CH 3 ;
• A is piperidinyl, phenyl, or pyridinyl, each substituted with -L-R4 and zero to 1 R4b;
• L is a bond, -CH 2 - — C(O)— , -C(O)CH 2 -, or -C(O)CH 2 CH 2 -;
• RI is hydrogen or -CH 3 ;
• R 3 is hydrogen or -CH 3 ;
• R4 is: (i) -N(CH 3 ) 2 ; or (ii) pyrrolidinyl, piperidinyl, piperazinyl, or pyridinyl, each substituted with zero to 2 R4 a ;
• R4a is independently -CH 3 , -CH
• a compound of Formula (I) or stereoisomers, tautomer, solvates or salts thereof wherein: X is C-A; Y is N; Qi is G; Q2 is R3; G is phenyl substituted with 2 substituents selected from -OCH3; A is piperidinyl or phenyl, each substituted with -L-R4; Ri is hydrogen or -CH3; R3 is -CH3; L is a bond, -C(O)- -C(O)CH2-, or -C(O)CH2CH2-; R4 is: (i) -N(CH3)2; or (ii) pyrrolidinyl, piperidinyl, piperazinyl, or pyridinyl, each substituted with zero to 2 R4 a ; R4a is independently -CH3, -CH(CH 3 )2, -CH 2 CH(CH 3 )2, -CH 2 C(CH 3 )3,
• a compound of Formula (I) or stereoisomers, tautomer, solvates or salts thereof wherein: X is C-A; Y is N; Qi is R3; Q2 is G; G is phenyl substituted with 2 substituents selected from -OCH3; A is piperidinyl or phenyl, each substituted with -L-R4; L is a bond; Ri is -CH3; R3 is -CH3; R4 is piperidinyl or piperazinyl, each substituted with R4 a ; R4a is independently -CH(CH3)2 or -CH2CH(CH3)2; and each R5 is hydrogen.
• a compound of Formula (I) or stereoisomers, tautomer, solvates or salts thereof wherein: X is N; Y is C-A; Qi is R3; Q2 is G; G is phenyl substituted with 1 to 2 substituents independently selected from -OCH3 and -S(O)2CH3; A is piperidinyl or phenyl, each substituted with -L-R4 and zero to 1 R4b; L is a bond, -CH2-, or -C(O)CH2-; Ri is -CH3; R3 is hydrogen; R4 is: piperidinyl, piperazinyl, or pyridinyl, each substituted with zero to 2 R4 a ; R4a is independently -CH3, -CH(CH 3 ) 2 , -CH 2 CH(CH 3 )2, -CF3, -CH 2 (cyclopropyl), -C(O)CH 3 , -C(O)
• One embodiment provides a compound of Formula (I) or stereoisomers, tautomer, solvates or salts thereof, wherein said compound is: 2-(3,4-dimethoxyphenyl)-5-(4-(4- isopropylpiperazin-l-yl)phenyl)-3-methyl-lH-pyrrolo[2,3-c]pyridine (1); or 2-(3,4- dimethoxyphenyl)-5-(r-isobutyl-[l,4'-bipiperidin]-4-yl)-l,3-dimethyl-lH-pyrrolo[2,3- c]pyridine (13).
• One embodiment provides a compound of Formula (I) or a salt thereof, wherein said compound is: 2-(3,4-dimethoxyphenyl)-5-(4-(4-isopropylpiperazin-l-yl)phenyl)-3- methyl-lH-pyrrolo[2,3-c]pyridine (2); l-(4-(4-(3-(3,4-dimethoxyphenyl)-l,2-dimethyl- lH-pyrrolo[2,3-c]pyridin-5-yl)phenyl)piperazin-l-yl)-2-methylpropan-2-ol (3); benzyl 4- (3-(3,4-dimethoxyphenyl)-2-methyl-lH-pyrrolo[2,3-c]pyridin-5-yl)-[l,4'-bipiperidine]-r- carboxylate (4); (l-cyclopropylpiperidin-4-yl)(4-(3-(3,4-dimeth
• One embodiment provides a compound of Formula (I) or stereoisomers, tautomer, solvates or salts thereof, wherein said compound is: ethyl 4-(2-(3,4-dimethoxyphenyl)-l- m ethyl- lH-pyrrolo[3 ,2-c]pyridin-6-yl)-[ 1 ,4'-bipiperidine]- 1 '-carboxylate (7); 2-(3 ,4- dimethoxyphenyl)-l-methyl-6-(l-((6-methylpyridin-3-yl)methyl)piperidin-4-yl)-lH- pyrrolo[3,2-c]pyridine (8); 6-(4-(4-(cyclopropylmethyl)piperazin-l-yl)phenyl)-2-(3,4- dimethoxyphenyl)-l-methyl-lH-pyrrolo[3,2-c]pyridine (9); 6-(4-(4-cyclobutyl
• One embodiment provides compounds of the Formula (I) having TLR9 ICso values of ⁇ 0.6 pM.
• One embodiment provides compounds of the Formula (I) having TLR9 ICso values of ⁇ 0.1 pM.
• One embodiment provides compounds of the Formula (I) having TLR9 ICso values of ⁇ 0.05 pM.
• One embodiment provides compounds of the Formula (I) having TLR9 ICso values of ⁇ 0.025 pM.
• One embodiment provides compounds of the Formula (I) having TLR9 ICso values of ⁇ 0.015 pM.
• One embodiment provides compounds of the Formula (I) having TLR9 ICso values of ⁇ 0.01 pM.
• the present invention provides a composition comprising at least one of the compounds of the present invention, or a stereoisomer, a tautomer, or a pharmaceutically acceptable salt or a solvate thereof.
• the present invention provides a pharmaceutical composition
• a pharmaceutical composition comprising a pharmaceutically acceptable carrier and at least one of the compounds of the present invention or a stereoisomer, a tautomer, or a pharmaceutically acceptable salt or a solvate thereof.
• the present invention provides a pharmaceutical composition, comprising a pharmaceutically acceptable carrier and a therapeutically effective amount of at least one of the compounds of the present invention or a stereoisomer, a tautomer, or a pharmaceutically acceptable salt or a solvate thereof.
• the present invention provides a process for making a compound of the present invention.
• the present invention provides an intermediate for making a compound of the present invention.
• the present invention provides a pharmaceutical composition as defined above further comprising one or more additional therapeutic agents.
• references made in the singular may also include the plural.
• references made in the singular may also include the plural.
• “a” and “an” may refer to either one, or one or more.
• a compound of Formula (I) includes a compound of Formula (I) and two or more compounds of Formula (I).
• any heteroatom with unsatisfied valences is assumed to have hydrogen atoms sufficient to satisfy the valences.
• halo and halogen, as used herein, refer to F, Cl, Br, and I.
• cyano refers to the group -CN.
• amino refers to the group -NH2.
• alkyl refers to both branched and straight-chain saturated aliphatic hydrocarbon groups containing, for example, from 1 to 12 carbon atoms, from 1 to 6 carbon atoms, and from 1 to 4 carbon atoms.
• alkyl groups include, but are not limited to, methyl (Me), ethyl (Et), propyl (e.g., n-propyl and i-propyl), butyl (e.g., n-butyl, i-butyl, sec-butyl, and /-butyl), and pentyl (e.g., n-pentyl, isopentyl, neopentyl), n-hexyl, 2-methylpentyl, 2-ethylbutyl, 3 -methylpentyl, and 4- methylpentyl.
• Me methyl
• Et ethyl
• propyl e.g., n-propyl and i-propyl
• butyl e.g., n-butyl, i-butyl, sec-butyl, and /-butyl
• pentyl e.g., n-p
• C When numbers appear in a subscript after the symbol “C”, the subscript defines with more specificity the number of carbon atoms that a particular group may contain.
• “Ci-6 alkyl” denotes straight and branched chain alkyl groups with one to six carbon atoms.
• fluoroalkyl as used herein is intended to include both branched and straight-chain saturated aliphatic hydrocarbon groups substituted with one or more fluorine atoms.
• Ci-4 fluoroalkyl is intended to include Ci, C2, C3, and C4 alkyl groups substituted with one or more fluorine atoms.
• Representative examples of fluoroalkyl groups include, but are not limited to, -CF3 and -CH2CF3.
• hydroxy alkyl includes both branched and straight-chain saturated alkyl groups substituted with one or more hydroxyl groups.
• hydroxy alkyl includes -CH2OH, -CH2CH2OH, and Ci-4 hydroxy alkyl.
• aminoalkyl includes both branched and straight-chain saturated alkyl groups substituted with one or more amine groups.
• aminoalkyl includes -CH2NH2, -CH2CH2NH2, and Ci-4 aminoalkyl.
• cyanoalkyl includes both branched and straight-chain saturated alkyl groups substituted with one or more cyano groups.
• aminoalkyl includes -CH2CN, -CH2CH2CN, and Ci-4 cyanoalkyl.
• alkoxy refers to an alkyl group attached to the parent molecular moiety through an oxygen atom, for example, methoxy group (-OCH3).
• -OCH3 methoxy group
• C1-3 alkoxy denotes alkoxy groups with one to three carbon atoms.
• fluoroalkoxy and -O(fluoroalkyl) represent a fluoroalkyl group as defined above attached through an oxygen linkage (-O-).
• -O- oxygen linkage
• Ci-4 fluoroalkoxy is intended to include Ci, C2, C3, and C4 fluoroalkoxy groups.
• alkoxyalkyl refers to an alkoxy group attached through its oxygen atom to an alkyl group, which is attached to the parent molecular moiety through a carbon atom, for example, methoxymethyl group (-CH2OCH3).
• -CH2OCH3 methoxymethyl group
• C2-4 alkoxyalkyl denotes alkoxyalkyl groups with two to four carbon atoms, such as -CH2OCH3, -CH2CH2OCH3, -CH2OCH2CH3, and -CH2CH2OCH2CH3.
• cycloalkyl refers to a group derived from a nonaromatic monocyclic or polycyclic hydrocarbon molecule by removal of one hydrogen atom from a saturated ring carbon atom.
• Representative examples of cycloalkyl groups include, but are not limited to, cyclopropyl, cyclopentyl, and cyclohexyl.
• the subscript defines with more specificity the number of carbon atoms that a particular cycloalkyl group may contain.
• C3-6 cycloalkyl denotes cycloalkyl groups with three to six carbon atoms.
• phrases “pharmaceutically acceptable” is employed herein to refer to those compounds, materials, compositions, and/or dosage forms which are, within the scope of sound medical judgment, suitable for use in contact with the tissues of human beings and animals without excessive toxicity, irritation, allergic response, or other problem or complication, commensurate with a reasonable benefit/risk ratio.
• the compounds of Formula (I) can be provided as amorphous solids or crystalline solids. Lyophilization can be employed to provide the compounds of Formula (I) as amorphous solids.
• solvates e.g., hydrates of the compounds of Formula (I) are also within the scope of the present invention.
• the term “solvate” means a physical association of a compound of Formula (I) with one or more solvent molecules, whether organic or inorganic. This physical association includes hydrogen bonding. In certain instances the solvate will be capable of isolation, for example when one or more solvent molecules are incorporated in the crystal lattice of the crystalline solid. “Solvate” encompasses both solution-phase and isolable solvates. Exemplary solvates include hydrates, ethanolates, methanolates, isopropanolates, acetonitrile solvates, and ethyl acetate solvates. Methods of solvation are known in the art.
• compounds of Formula (I), subsequent to their preparation, can be isolated and purified to obtain a composition containing an amount by weight equal to or greater than 99% of a compound of Formula (I), respectively (“substantially pure”), which is then used or formulated as described herein.
• substantially pure compounds of Formula (I) are also contemplated herein as part of the present invention.
• “Stable compound” and “stable structure” are meant to indicate a compound that is sufficiently robust to survive isolation to a useful degree of purity from a reaction mixture, and formulation into an efficacious therapeutic agent.
• the present invention is intended to embody stable compounds.
• “Therapeutically effective amount” is intended to include an amount of a compound of the present invention alone or an amount of the combination of compounds claimed or an amount of a compound of the present invention in combination with other active ingredients effective to act as an inhibitor of TLR9, or effective to treat or prevent disorders associated with a fibrotic disease or disorder, dysregulation of bile acids, such as pathological fibrosis.
• treating cover the treatment of a disease-state in a mammal, particularly in a human, and include: (a) preventing the disease-state from occurring in a mammal, in particular, when such mammal is predisposed to the diseasestate but has not yet been diagnosed as having it; (b) inhibiting the disease-state, i.e., arresting its development; and/or (c) relieving the disease-state, i.e., causing regression of the disease state.
• the compounds of the present invention are intended to include all isotopes of atoms occurring in the present compounds.
• Isotopes include those atoms having the same atomic number but different mass numbers.
• isotopes of hydrogen include deuterium (D) and tritium (T).
• Isotopes of carbon include 13 C and 14 C.
• Isotopically-labeled compounds of the invention can generally be prepared by conventional techniques known to those skilled in the art or by processes analogous to those described herein, using an appropriate isotopically-labeled reagent in place of the non-labeled reagent otherwise employed.
• methyl (- CH3) also includes deuterated methyl groups such as -CD3.
• the compounds of the invention are useful for inhibiting the TLR9 receptor.
• One embodiment provides a method for the treatment of a disease, disorder, or condition associated with dysregulation of bile acids in a patient in need of such treatment, and the method comprises administering a therapeutically effective amount of a compound of the present invention, or a stereoisomer, a tautomer, or a pharmaceutically acceptable salt or solvate thereof, to the patient.
• One embodiment provides a method for the treatment of a disease, disorder, or condition associated with activity of the TLR9 receptor in a patient in need of such treatment comprising administering a therapeutically effective amount of a compound of the present invention, or a stereoisomer, a tautomer, or a pharmaceutically acceptable salt or solvate thereof, to the patient.
• One embodiment provides a method for the treatment of the disease, disorder, or condition comprising administering to a patient in need of such treatment a therapeutically effective amount of at least one of the compounds of the present invention, alone, or, optionally, in combination with another compound of the present invention and/or at least one other type of therapeutic agent.
• One embodiment provides a method for eliciting an TLR9 receptor agonizing effect in a patient comprising administering a therapeutically effective amount of a compound of the present invention, or a stereoisomer, a tautomer, or a pharmaceutically acceptable salt or solvate thereof, to the patient.
• the disease, disorder, or condition is associated with TLR9 dysfunction include pathological fibrosis, cancer, inflammatory disorders, metabolic, or cholestatic disorders.
• the disease, disorder, or condition is associated with fibrosis, including liver, biliary, renal, cardiac, dermal, ocular, and pancreatic fibrosis.
• the disease, disorder, or condition is associated with cell- proliferative disorders, such as cancer.
• the cancer includes solid tumor growth or neoplasia.
• the cancer includes tumor metastasis.
• the cancer is of the liver, gall bladder, small intestine, large intestine, kidney, prostate, bladder, blood, bone, brain, breast, central nervous system, cervix, colon, endometrium, esophagus, genitalia, genitourinary tract, head, larynx, lung, muscle tissue, neck, oral or nasal mucosa, ovary, pancreas, skin, spleen, stomach, testicle, or thyroid.
• the cancer is a carcinoma, sarcoma, lymphoma, leukemia, melanoma, mesothelioma, multiple myeloma, or seminoma.
• diseases, disorders, or conditions associated with the activity of FXR include, but are not limited to, transplant injection, fibrotic disorders (e. g., liver fibrosis, kidney fibrosis), inflammatory disorders (e.g., acute hepatitis, chronic hepatitis, non-alcoholic steatohepatitis (NASH), irritable bowel syndrome (IBS), inflammatory bowel disease (IBD)), as well as cell-proliferative disorders (e.g., cancer, myeloma, fibroma, hepatocellular carcinoma, colorectal cancer, prostate cancer, leukemia, Kaposi’s sarcoma, solid tumors).
• fibrotic disorders e. g., liver fibrosis, kidney fibrosis
• inflammatory disorders e.g., acute hepatitis, chronic hepatitis, non-alcoholic steatohepatitis (NASH), irritable bowel syndrome (IBS), inflammatory bowel disease (IBD)
• fibrotic disorders, inflammatory disorders, as well as cell-proliferative disorders include, but are not limited to, non-alcoholic fatty liver disease (NAFLD), alcoholic or non-alcoholic steatohepatitis (NASH), acute hepatitis, chronic hepatitis, liver cirrhosis, primary biliary cirrhosis, primary sclerosing cholangitis, drug-induced hepatitis, biliary cirrhosis, portal hypertension, regenerative failure, liver hypofunction, hepatic blood flow disorder, nephropathy, irritable bowel syndrome (IBS), inflammatory bowel disease (IBD), abnormal pancreatic secretion, benign prostatic hyperplasia, neuropathic bladder disease, diabetic nephropathy, focal segmental glomerulosclerosis, IgA nephropathy, nephropathy induced by drugs or transplantation, autoimmune nephropathy, l
• NAFLD non-alcoholic fatty liver disease
• the present invention provides a method for the treatment of a fibrotic disorder, an inflammatory disorder, or a cell-proliferative disorder, comprising administering to a patient in need of such treatment a therapeutically effective amount of at least one of the compounds of the present invention, alone, or, optionally, in combination with another compound of the present invention and/or at least one other type of therapeutic agent.
• the present invention provides a compound of the present invention for use in therapy.
• the present invention provides a compound of the present invention for use in therapy for the treatment of a fibrotic disorder, an inflammatory disorder, or a cell-proliferative disorder thereof.
• the present invention also provides the use of a compound of the present invention for the manufacture of a medicament for the treatment of a fibrotic disorder, an inflammatory disorder, or a cell-proliferative disorder thereof.
• the present invention provides a method for the treatment of a fibrotic disorder, an inflammatory disorder, or a cell-proliferative disorder, comprising administering to a patient in need thereof a therapeutically effective amount of a first and second therapeutic agent, wherein the first therapeutic agent is a compound of the present invention.
• the present invention provides a combined preparation of a compound of the present invention and additional therapeutic agent(s) for simultaneous, separate or sequential use in therapy.
• the present invention provides a combined preparation of a compound of the present invention and additional therapeutic agent(s) for simultaneous, separate or sequential use in the treatment of a fibrotic disorder, an inflammatory disorder, or a cell-proliferative disorder.
• the compounds of the present invention may be employed in combination with additional therapeutic agent(s), such as one or more anti-fibrotic and/or anti-inflammatory therapeutic agents.
• additional therapeutic agent(s) used in combined pharmaceutical compositions or combined methods or combined uses are selected from one or more, preferably one to three, of the following therapeutic agents: TGF0 receptor inhibitors (for example, galunisertib), inhibitors of TGF0 synthesis (for example, pirfenidone), inhibitors of vascular endothelial growth factor (VEGF), platelet-derived growth factor (PDGF) and fibroblast growth factor (FGF) receptor kinases (for example, nintedanib), humanized anti-avP6 integrin monoclonal antibody (for example, 3G9), human recombinant pentraxin-2, recombinant human Serum Amyloid P, recombinant human antibody against TGF0-1, -2, and -3, endothelin receptor antagonists (for example, macitentan), interferon gamma, c-Jun amino-terminal kinase (JNK) inhibitor (for example, 4-[[9-[(3S), 5-fluor
• the therapeutic agents useful for the treatment of such fibrotic conditions include, but are not limited to, FXR agonists (for example OCA, GS-9674, and LJN452), LOXL2 inhibitors (for example pumpuzumab), LPA1 antagonists (for example, BMS- 986020 and SAR 100842), PPAR modulators (for example, elafibrinor, pioglitazone, and saroglitazar, IVA337), SSAO/VAP-1 inhibitors (for example, PXS-4728A and SZE5302), ASK-1 inhibitors (for example GS-4997 or selonsertib), ACC inhibitors (for example, CP-640186 and NDL010976 or GS-0976), FGF21 mimetics (for example, LY2405319 and BMS-986036), caspase inhibitors (for example, emricasan), N0X4 inhibitors (for example, GKT137831),
• additional therapeutic agent(s) used in combined pharmaceutical compositions or combined methods or combined uses are selected from one or more, preferably one to three, of immunoncology agents, such as Alemtuzumab, Atezolizumab, Ipilimumab, Nivolumab, Ofatumumab, Pembrolizumab, and Rituximab.
• immunoncology agents such as Alemtuzumab, Atezolizumab, Ipilimumab, Nivolumab, Ofatumumab, Pembrolizumab, and Rituximab.
• the above other therapeutic agents when employed in combination with the compounds of the present invention, may be used, for example, in those amounts indicated in the Physicians' Desk Reference (PDR) or as otherwise determined by one of ordinary skill in the art.
• PDR Physicians' Desk Reference
• such other therapeutic agent(s) may be administered prior to, simultaneously with, or following the administration of the inventive compounds.
• the present invention also provides pharmaceutical compositions capable of treating TLR9-associated conditions.
• inventive compositions may contain other therapeutic agents as described above and may be formulated, for example, by employing conventional solid or liquid vehicles or diluents, as well as pharmaceutical additives of a type appropriate to the mode of desired administration (e.g., excipients, binders, preservatives, stabilizers, flavors, etc.) according to techniques such as those well known in the art of pharmaceutical formulation.
• pharmaceutical additives e.g., excipients, binders, preservatives, stabilizers, flavors, etc.
• compositions comprising one or more compounds of Formula (I) and a pharmaceutically acceptable carrier.
• a “pharmaceutically acceptable carrier” refers to media generally accepted in the art for the delivery of biologically active agents to animals, in particular, mammals.
• Pharmaceutically acceptable carriers are formulated according to a number of factors well within the purview of those of ordinary skill in the art. These include without limitation the type and nature of the active agent being formulated; the subject to which the agentcontaining composition is to be administered; the intended route of administration of the composition; and, the therapeutic indication being targeted.
• Pharmaceutically acceptable carriers include both aqueous and non-aqueous liquid media, as well as a variety of solid and semi-solid dosage forms.
• Such carriers can include a number of different ingredients and additives in addition to the active agent, such additional ingredients being included in the formulation for a variety of reasons, e.g., stabilization of the active agent, binders, etc., well known to those of ordinary skill in the art.
• suitable pharmaceutically acceptable carriers, and factors involved in their selection are found in a variety of readily available sources such as, for example, Remington: The Science and Practice of Pharmacy, 22 nd Edition (2013).
• Compounds in accordance with Formula (I) can be administered by any means suitable for the condition to be treated, which can depend on the need for site-specific treatment or quantity of Formula (I) compound to be delivered.
• the compounds of Formula (I) may be administered by any suitable route, preferably in the form of a pharmaceutical composition adapted to such a route, and in a dose effective for the treatment intended.
• the compounds and compositions of the present invention may, for example, be administered orally, mucosally, or parentally including intravascularly, intravenously, intraperitoneally, subcutaneously, intramuscularly, and intrasternally in dosage unit formulations containing conventional pharmaceutically acceptable carriers, adjuvants, and vehicles.
• the pharmaceutical carrier may contain a mixture of mannitol or lactose and microcrystalline cellulose.
• the mixture may contain additional components such as a lubricating agent, e.g. magnesium stearate and a disintegrating agent such as crospovidone.
• the carrier mixture may be filled into a gelatin capsule or compressed as a tablet.
• the pharmaceutical composition may be administered as an oral dosage form or an infusion, for example.
• the pharmaceutical composition may be in the form of, for example, a tablet, capsule, liquid capsule, suspension, or liquid.
• the pharmaceutical composition is preferably made in the form of a dosage unit containing a particular amount of the active ingredient.
• the pharmaceutical composition may be provided as a tablet or capsule comprising an amount of active ingredient in the range of from about 0.1 to 1000 mg, preferably from about 0.25 to 250 mg, and more preferably from about 0.5 to 100 mg.
• a suitable daily dose for a human or other mammal may vary widely depending on the condition of the patient and other factors, but, can be determined using routine methods.
• any pharmaceutical composition contemplated herein can, for example, be delivered orally via any acceptable and suitable oral preparations.
• exemplary oral preparations include, but are not limited to, for example, tablets, troches, lozenges, aqueous and oily suspensions, dispersible powders or granules, emulsions, hard and soft capsules, liquid capsules, syrups, and elixirs.
• Pharmaceutical compositions intended for oral administration can be prepared according to any methods known in the art for manufacturing pharmaceutical compositions intended for oral administration.
• a pharmaceutical composition in accordance with the invention can contain at least one agent selected from sweetening agents, flavoring agents, coloring agents, demulcents, antioxidants, and preserving agents.
• a tablet can, for example, be prepared by admixing at least one compound of Formula (I) with at least one non-toxic pharmaceutically acceptable excipient suitable for the manufacture of tablets.
• excipients include, but are not limited to, for example, inert diluents, such as, for example, calcium carbonate, sodium carbonate, lactose, calcium phosphate, and sodium phosphate; granulating and disintegrating agents, such as, for example, microcrystalline cellulose, sodium crosscarmellose, com starch, and alginic acid; binding agents, such as, for example, starch, gelatin, polyvinyl-pyrrolidone, and acacia; and lubricating agents, such as, for example, magnesium stearate, stearic acid, and talc.
• inert diluents such as, for example, calcium carbonate, sodium carbonate, lactose, calcium phosphate, and sodium phosphate
• granulating and disintegrating agents such as, for
• a tablet can either be uncoated, or coated by known techniques to either mask the bad taste of an unpleasant tasting drug, or delay disintegration and absorption of the active ingredient in the gastrointestinal tract thereby sustaining the effects of the active ingredient for a longer period.
• exemplary water soluble taste masking materials include, but are not limited to, hydroxypropyl-methylcellulose and hydroxypropyl-cellulose.
• Exemplary time delay materials include, but are not limited to, ethyl cellulose and cellulose acetate butyrate.
• Hard gelatin capsules can, for example, be prepared by mixing at least one compound of Formula (I) with at least one inert solid diluent, such as, for example, calcium carbonate; calcium phosphate; and kaolin.
• at least one inert solid diluent such as, for example, calcium carbonate; calcium phosphate; and kaolin.
• Soft gelatin capsules can, for example, be prepared by mixing at least one compound of Formula (I) with at least one water soluble carrier, such as, for example, polyethylene glycol; and at least one oil medium, such as, for example, peanut oil, liquid paraffin, and olive oil.
• at least one water soluble carrier such as, for example, polyethylene glycol
• at least one oil medium such as, for example, peanut oil, liquid paraffin, and olive oil.
• An aqueous suspension can be prepared, for example, by admixing at least one compound of Formula (I) with at least one excipient suitable for the manufacture of an aqueous suspension.
• excipients suitable for the manufacture of an aqueous suspension include, but are not limited to, for example, suspending agents, such as, for example, sodium carboxymethylcellulose, methylcellulose, hydroxypropylmethyl- cellulose, sodium alginate, alginic acid, polyvinyl-pyrrolidone, gum tragacanth, and gum acacia; dispersing or wetting agents, such as, for example, a naturally-occurring phosphatide, e.g., lecithin; condensation products of alkylene oxide with fatty acids, such as, for example, polyoxyethylene stearate; condensation products of ethylene oxide with long chain aliphatic alcohols, such as, for example heptadecaethylene-oxycetanol; condensation products of ethylene oxide with partial esters derived from fatty acids and
• An aqueous suspension can also contain at least one preservative, such as, for example, ethyl and n- propyl p-hydroxybenzoate; at least one coloring agent; at least one flavoring agent; and/or at least one sweetening agent, including but not limited to, for example, sucrose, saccharin, and aspartame.
• Oily suspensions can, for example, be prepared by suspending at least one compound of Formula (I) in either a vegetable oil, such as, for example, arachis oil; olive oil; sesame oil; and coconut oil; or in mineral oil, such as, for example, liquid paraffin.
• An oily suspension can also contain at least one thickening agent, such as, for example, beeswax; hard paraffin; and cetyl alcohol.
• at least one of the sweetening agents already described hereinabove, and/or at least one flavoring agent can be added to the oily suspension.
• An oily suspension can further contain at least one preservative, including, but not limited to, for example, an antioxidant, such as, for example, butylated hydroxyanisol, and alpha-tocopherol.
• Dispersible powders and granules can, for example, be prepared by admixing at least one compound of Formula (I) with at least one dispersing and/or wetting agent; at least one suspending agent; and/or at least one preservative.
• Suitable dispersing agents, wetting agents, and suspending agents are as already described above.
• Exemplary preservatives include, but are not limited to, for example, anti-oxidants, e.g., ascorbic acid.
• dispersible powders and granules can also contain at least one excipient, including, but not limited to, for example, sweetening agents; flavoring agents; and coloring agents.
• An emulsion of at least one compound of Formula (I) thereof can, for example, be prepared as an oil-in-water emulsion.
• the oily phase of the emulsions comprising compounds of Formula (I) may be constituted from known ingredients in a known manner.
• the oil phase can be provided by, but is not limited to, for example, a vegetable oil, such as, for example, olive oil and arachis oil; a mineral oil, such as, for example, liquid paraffin; and mixtures thereof. While the phase may comprise merely an emulsifier, it may comprise a mixture of at least one emulsifier with a fat or an oil or with both a fat and an oil.
• Suitable emulsifying agents include, but are not limited to, for example, naturally-occurring phosphatides, e.g., soy bean lecithin; esters or partial esters derived from fatty acids and hexitol anhydrides, such as, for example, sorbitan monooleate; and condensation products of partial esters with ethylene oxide, such as, for example, polyoxyethylene sorbitan monooleate.
• a hydrophilic emulsifier is included together with a lipophilic emulsifier which acts as a stabilizer. It is also preferred to include both an oil and a fat.
• emulsifier(s) with or without stabilizer(s) make-up the so-called emulsifying wax
• the wax together with the oil and fat make up the so-called emulsifying ointment base which forms the oily dispersed phase of the cream formulations.
• An emulsion can also contain a sweetening agent, a flavoring agent, a preservative, and/or an antioxidant.
• Emulsifiers and emulsion stabilizers suitable for use in the formulation of the present invention include Tween 60, Span 80, cetostearyl alcohol, myristyl alcohol, glyceryl monostearate, sodium lauryl sulfate, glyceryl distearate alone or with a wax, or other materials well known in the art.
• the compounds of Formula (I) can, for example, also be delivered intravenously, subcutaneously, and/or intramuscularly via any pharmaceutically acceptable and suitable injectable form.
• injectable forms include, but are not limited to, for example, sterile aqueous solutions comprising acceptable vehicles and solvents, such as, for example, water, Ringer’s solution, and isotonic sodium chloride solution; sterile oil-in- water microemulsions; and aqueous or oleaginous suspensions.
• Formulations for parenteral administration may be in the form of aqueous or nonaqueous isotonic sterile injection solutions or suspensions. These solutions and suspensions may be prepared from sterile powders or granules using one or more of the carriers or diluents mentioned for use in the formulations for oral administration or by using other suitable dispersing or wetting agents and suspending agents.
• the compounds may be dissolved in water, polyethylene glycol, propylene glycol, ethanol, com oil, cottonseed oil, peanut oil, sesame oil, benzyl alcohol, sodium chloride, tragacanth gum, and/or various buffers. Other adjuvants and modes of administration are well and widely known in the pharmaceutical art.
• the active ingredient may also be administered by injection as a composition with suitable carriers including saline, dextrose, or water, or with cyclodextrin (i.e. Captisol), cosolvent solubilization (i.e. propylene glycol) or micellar solubilization (i.e. Tween 80).
• suitable carriers including saline, dextrose, or water, or with cyclodextrin (i.e. Captisol), cosolvent solubilization (i.e. propylene glycol) or micellar solubilization (i.e. Tween 80).
• the sterile injectable preparation may also be a sterile injectable solution or suspension in a non-toxic parenterally acceptable diluent or solvent, for example as a solution in 1,3 -butanediol.
• a non-toxic parenterally acceptable diluent or solvent for example as a solution in 1,3 -butanediol.
• acceptable vehicles and solvents that may be employed are water, Ringer’s solution, and isotonic sodium chloride solution.
• sterile, fixed oils are conventionally employed as a solvent or suspending medium.
• any bland fixed oil may be employed, including synthetic mono- or diglycerides.
• fatty acids such as oleic acid find use in the preparation of injectables.
• a sterile injectable oil-in-water microemulsion can, for example, be prepared by 1) dissolving at least one compound of Formula (I) in an oily phase, such as, for example, a mixture of soybean oil and lecithin; 2) combining the Formula (I) containing oil phase with a water and glycerol mixture; and 3) processing the combination to form a microemulsion.
• an oily phase such as, for example, a mixture of soybean oil and lecithin
• combining the Formula (I) containing oil phase with a water and glycerol mixture and 3) processing the combination to form a microemulsion.
• a sterile aqueous or oleaginous suspension can be prepared in accordance with methods already known in the art.
• a sterile aqueous solution or suspension can be prepared with a non-toxic parenterally-acceptable diluent or solvent, such as, for example, 1,3-butane diol; and a sterile oleaginous suspension can be prepared with a sterile non-toxic acceptable solvent or suspending medium, such as, for example, sterile fixed oils, e.g., synthetic mono- or diglycerides; and fatty acids, such as, for example, oleic acid.
• Pharmaceutically acceptable carriers, adjuvants, and vehicles that may be used in the pharmaceutical compositions of this invention include, but are not limited to, ion exchangers, alumina, aluminum stearate, lecithin, self-emulsifying drug delivery systems (SEDDS) such as d-alpha-tocopherol polyethyleneglycol 1000 succinate, surfactants used in pharmaceutical dosage forms such as Tweens, polyethoxylated castor oil such as CREMOPHOR surfactant (BASF), or other similar polymeric delivery matrices, serum proteins, such as human serum albumin, buffer substances such as phosphates, glycine, sorbic acid, potassium sorbate, partial glyceride mixtures of saturated vegetable fatty acids, water, salts or electrolytes, such as protamine sulfate, disodium hydrogen phosphate, potassium hydrogen phosphate, sodium chloride, zinc salts, colloidal silica, magnesium trisilicate, polyvinyl pyrrolidone, cellulose
• Cyclodextrins such as alpha-, beta-, and gamma-cyclodextrin, or chemically modified derivatives such as hydroxyalkylcyclodextrins, including 2- and 3-hydroxypropyl-cyclodextrins, or other solubilized derivatives may also be advantageously used to enhance delivery of compounds of the formulae described herein.
• the pharmaceutically active compounds of this invention can be processed in accordance with conventional methods of pharmacy to produce medicinal agents for administration to patients, including humans and other mammals.
• the pharmaceutical compositions may be subjected to conventional pharmaceutical operations such as sterilization and/or may contain conventional adjuvants, such as preservatives, stabilizers, wetting agents, emulsifiers, buffers etc. Tablets and pills can additionally be prepared with enteric coatings.
• Such compositions may also comprise adjuvants, such as wetting, sweetening, flavoring, and perfuming agents.
• the amounts of compounds that are administered and the dosage regimen for treating a disease condition with the compounds and/or compositions of this invention depends on a variety of factors, including the age, weight, sex, the medical condition of the subject, the type of disease, the severity of the disease, the route and frequency of administration, and the particular compound employed. Thus, the dosage regimen may vary widely, but can be determined routinely using standard methods.
• the daily dose can be administered in one to four doses per day. Other dosing schedules include one dose per week and one dose per two day cycle.
• the active compounds of this invention are ordinarily combined with one or more adjuvants appropriate to the indicated route of administration.
• the compounds may be admixed with lactose, sucrose, starch powder, cellulose esters of alkanoic acids, cellulose alkyl esters, talc, stearic acid, magnesium stearate, magnesium oxide, sodium and calcium salts of phosphoric and sulfuric acids, gelatin, acacia gum, sodium alginate, polyvinylpyrrolidone, and/or polyvinyl alcohol, and then tableted or encapsulated for convenient administration.
• Such capsules or tablets may contain a controlled-release formulation as may be provided in a dispersion of active compound in hydroxypropylmethyl cellulose.
• compositions of this invention comprise at least one compound of Formula (I) and optionally an additional agent selected from any pharmaceutically acceptable carrier, adjuvant, and vehicle.
• Alternate compositions of this invention comprise a compound of the Formula (I) described herein, or a prodrug thereof, and a pharmaceutically acceptable carrier, adjuvant, or vehicle.
• the present invention also encompasses an article of manufacture.
• article of manufacture is intended to include, but not be limited to, kits and packages.
• the article of manufacture of the present invention comprises: (a) a first container; (b) a pharmaceutical composition located within the first container, wherein the composition, comprises: a first therapeutic agent, comprising: a compound of the present invention or a pharmaceutically acceptable salt form thereof; and, (c) a package insert stating that the pharmaceutical composition can be used for the treatment of a cardiovascular disorder, diuresis, and/or natriuresis.
• the package insert states that the pharmaceutical composition can be used in combination (as defined previously) with a second therapeutic agent to treat cardiovascular disorder, diuresis, and/or natriuresis.
• the article of manufacture can further comprise: (d) a second container, wherein components (a) and (b) are located within the second container and component (c) is located within or outside of the second container. Located within the first and second containers means that the respective container holds the item within its boundaries.
• the first container is a receptacle used to hold a pharmaceutical composition.
• This container can be for manufacturing, storing, shipping, and/or individual/bulk selling.
• First container is intended to cover a bottle, jar, vial, flask, syringe, tube (e.g., for a cream preparation), or any other container used to manufacture, hold, store, or distribute a pharmaceutical product.
• the second container is one used to hold the first container and, optionally, the package insert.
• the second container include, but are not limited to, boxes (e.g., cardboard or plastic), crates, cartons, bags (e.g., paper or plastic bags), pouches, and sacks.
• the package insert can be physically attached to the outside of the first container via tape, glue, staple, or another method of attachment, or it can rest inside the second container without any physical means of attachment to the first container.
• the package insert is located on the outside of the second container. When located on the outside of the second container, it is preferable that the package insert is physically attached via tape, glue, staple, or another method of attachment. Alternatively, it can be adjacent to or touching the outside of the second container without being physically attached.
• the package insert is a label, tag, marker, or other written sheet that recites information relating to the pharmaceutical composition located within the first container.
• the information recited will usually be determined by the regulatory agency governing the area in which the article of manufacture is to be sold (e.g., the United States Food and Drug Administration).
• the package insert specifically recites the indications for which the pharmaceutical composition has been approved.
• the package insert may be made of any material on which a person can read information contained therein or thereon.
• the package insert is a printable material (e.g., paper, plastic, cardboard, foil, adhesive-backed paper or plastic) on which the desired information has been formed (e.g., printed or applied).
• the compounds of the present invention can be prepared in a number of ways well known to one skilled in the art of organic synthesis.
• the compounds of the present invention can be synthesized using the methods described below, together with synthetic methods known in the art of synthetic organic chemistry, or variations thereon as appreciated by those skilled in the art. Preferred methods include, but are not limited to, those described below.
• Scheme 1 describes the synthesis of compounds of Formula (I) and (I’).
• Cyclization of la and alkyne lb in the presence of a palladium catalyst such as bis(triphenylphosphine)palladium(II) chloride together with copper(I) iodide can supply 1c and Id.
• N-alkylation of 1c can provide le.
• Suzuki coupling of le with boronate ester If can afford the compounds of Formula (I) or the precursor to (I).
• Suzuki coupling of le with boronate ester 1g can yield Ih, which can be converted to the compounds of Formula (F) by hydrogenation, deprotection, and further modifications.
• Scheme 2 describes the synthesis of compounds of Formula (II) and (II’).
• N- alkylation of Id obtained from the cyclization of la and alkyne lb in Scheme, can provide If.
• Suzuki coupling of If with boronate ester 1g can afford the compounds of Formula (II) or the precursor to (II).
• Suzuki coupling of If with boronate ester Ih can yield i, which can be converted to the compounds of Formula (IL) by hydrogenation, deprotection, and further modifications.
• the phrase “dried and concentrated” generally refers to drying of a solution in an organic solvent over either sodium sulfate or magnesium sulfate, followed by filtration and removal of the solvent from the filtrate (generally under reduced pressure and at a temperature suitable to the stability of the material being dried and concentrated).
• reaction mixture Upon cooling to room temperature, the reaction mixture was diluted with methanol, filtered through an acrodisc, and injected to preparative HPLC (Column: Phenomenex Luna AXIA 5u C18 21.2 x 100. Solvent A: 90% H2O-10% methanol-0.1%TF A; Solvent B: 10% methanol-90% H2O 0.1% TFA. Flow rate: 20 mL/min. Gradient Time: 15 minutes. Start %B: 10; Final %B: 100). The correct fractions were concentrated under vacuum, basified with 1 N NaOH solution, and extracted with dichloromethane (4 x 40 mL). The combined extract was dried over anhydrous Na2SO4.
• reaction mixture Upon cooling to room temperature, the reaction mixture was diluted with methanol, filtered through an acrodisc, and injected to preparative HPLC (Column: Phenomenex Luna AXIA 5u Cl 8 21.2 x 100. Solvent A: 90% 1420-10% methanol - 0.1%TFA; Solvent B: 10% methanol-90% H2O 0.1% TFA. Flow rate: 20 mL/min. Gradient Time: 15 minutes. Start %B: 8; Final %B: 100). The correct fractions were concentrated under vacuum, basified with 1 N NaOH solution, and extracted with dichloromethane (4 x 40 mL). The combined extract was dried over anhydrous Na2SO4 .
• reaction mixture Upon cooling to room temperature, the reaction mixture was diluted with methanol, filtered through an acrodisc, and injected to preparative HPLC (Column: Phenomenex Luna AXIA 5u C18 21.2 x 100. Solvent A: 90% H2O-10% methanol-0.1%TFA; Solvent B: 10% methanol-90% H2O 0.1% TFA. Flow rate: 20 mL/min. Gradient Time: 15 minutes. Start %B: 15; Final %B: 100). The correct fractions were concentrated under vacuum, basified with 1 N NaOH solution, and extracted with dichloromethane (4 x 40 mL). The combined extract was dried over anhydrous Na2SO4.
• Step 1 Benzyl 4-(3-(3,4-dimethoxyphenyl)-2-methyl-lH-pyrrolo[2,3-c]pyridin-5-yl)-3,6- dihydropyridine- 1 (2H)-carboxylate
• a mixture of 5-chloro-3-(3,4-dimethoxyphenyl)-2-methyl-lH-pyrrolo[2,3-c] pyridine (408 mg, 1.348 mmol)
• benzyl 4-(4,4,5,5-tetramethyl-l,3,2-dioxaborolan-2-yl)- 3,6-dihydropyridine-l(2H)-carboxylate 555 mg, 1.617 mmol
• the heterogeneous mixture was diluted with ethyl acetate (10 mL) and filtered through Celite. The filtrate was concentrated under vacuum. The residue was diluted with methanol and injected to preparative HPLC (Column: Phenomenex Luna AXIA 5u Cl 8 21.2 x 100. Solvent A: 90% H2O-10% methanol-0.1%TF A; Solvent B: 10% methanol-90% H2O 0.1% TFA. Flow rate: 20 mL/min. Gradient Time: 15 minutes. Start %B: 16; Final %B: 100). The correct fractions were concentrated under vacuum, basified with 2 N NaOH solution, and extracted with dichloromethane (4 x 30 mL).
• the heterogeneous mixture was diluted with ethyl acetate (10 mL) and filtered through Celite. The filtrate was concentrated under vacuum. The residue was diluted with methanol and injected to preparative HPLC (Column: Phenomenex Luna AXIA 5u Cl 8 21.2 x 100. Solvent A: 90% HzO-10% methanol-0.1%TF A; Solvent B: 10% methanol-90% H2O 0.1% TFA. Flow rate: 20 mL/min. Gradient Time: 15 minutes. Start %B: 12; Final %B: 100). The correct fractions were concentrated under vacuum, basified with 1 N NaOH solution, and extracted with dichloromethane (4 x 30 mL).
• Step 1 l-(Cyclopropylmethyl)-4-(4-(4,4,5,5-tetramethyl-l,3,2-dioxaborolan-2-yl)phenyl) piperazine
• reaction mixture Upon cooling to room temperature, the reaction mixture was diluted with methanol, filtered through an acrodisc, and injected to preparative HPLC (Column: Phenomenex Luna AXIA 5u Cl 8 21.2 x 100. Solvent A: 90% H2O-10% methanol-0.1%TF A; Solvent B: 10% methanol-90% H2O 0.1% TFA. Flow rate: 20 mL/min. Gradient Time: 15 minutes. Start %B: 15; Final %B: 100). The correct fractions were concentrated under vacuum, basified with 1 N NaOH solution, and extracted with dichloromethane (4 x 40 mL). The combined extract was dried over anhydrous Na2SO4.
• Step 1 l-Cyclobutyl-4-(4-(4,4,5,5-tetramethyl-l,3,2-dioxaborolan-2-yl)phenyl) piperazine
• reaction mixture Upon cooling to room temperature, the reaction mixture was diluted with methanol, filtered through an acrodisc, and injected to preparative HPLC (Column: Phenomenex Luna AXIA 5u C18 21.2 x 100. Solvent A: 90% H2O-10% methanol-0.1%TF A; Solvent B: 10% methanol-90% H2O 0.1% TFA. Flow rate: 20 mL/min. Gradient Time: 15 minutes. Start %B: 15; Final %B: 100). The correct fractions were concentrated under vacuum, basified with 1 N NaOH, and extracted with dichloromethane (4 x 40 mL). The combined extract was dried over anhydrous Na2SO4.
• Solvent A 90% H2O- 10% methanol-0.1%TFA
• Solvent B 10% methanol-90% H2O 0.1% TFA.
• Flow rate 40 mL/min.
• Gradient Time 12 minutes. Start %B: 11; Final %B: 100).
• the correct fractions were combined, concentrated under vacuum, basified with saturated NaHCOs solution to pH 10, and extracted with dichloromethane (3 x 50 mL). The combined extract was dried over anhydrous MgSOi.
• reaction mixture Upon cooling to room temperature, the reaction mixture was diluted with methanol, filtered through an acrodisc, and injected to preparative HPLC (Phenomenex Luna AXIA 5u C18 30.0 x 100. Solvent A: 90% H2O-10% methanol- 0.1%TFA; Solvent B: 10% methanol-90% H2O 0.1% TFA. Flow rate: 40 mL/min. Gradient Time: 15 minutes. Start %B: 10; Final %B: 100). The correct fractions were concentrated under vacuum, basified with 1 N NaOH, and extracted with dichloromethane (4 x 40 mL). The combined extract was dried over anhydrous Na2SO4.
• Step 4 l-(2-Fluoro-4-(4,4,5,5-tetramethyl-l,3,2-dioxaborolan-2-yl)phenyl)-4- i sopropylpiperazine
• reaction mixture Upon cooling to room temperature, the reaction mixture was diluted with methanol, filtered through an acrodisc, and injected to preparative HPLC (Column: Phenomenex Luna AXIA 5u Cl 8 21.2 x 100. Solvent A: 90% H 2 O-10% methanol-0.1%TF A; Solvent B: 10% methanol-90% H 2 O 0.1% TFA. Flow rate: 20 mL/min. Gradient Time: 15 minutes. Start %B: 11; Final %B: 100). The correct fractions were concentrated under vacuum, basified with 1 N NaOH, and extracted with dichloromethane (4 x 40 mL).
• Examples 13-33 in Table 1 were prepared according to the synthetic routes described for the preparation of example 1-12.
• Step 1 tert-butyl 4-(4-(l,4-dimethyl-2-(4-(methylsulfonyl)phenyl)-lH-pyrrolo[3,2-c] pyridin-6-yl)phenyl)piperidine-l -carboxylate
• Step 1 4-(l,4-Dimethyl-2-(4-(methylsulfonyl)phenyl)-lH-pyrrolo[3,2-c]pyridin-6-yl) benzaldehyde
• Step 2 l-(4-(4-(l,4-Dimethyl-2-(4-(methylsulfonyl)phenyl)-lH-pyrrolo[3,2-c]pyridin-6- yl)benzyl)piperazin- 1 -yl)-2-methylpropan-2-ol
• Step 1 tert-Butyl (lR,4R)-5-(4-(l,4-dimethyl-2-(4-(methylsulfonyl)phenyl)-lH- pyrrolo[3,2-c]pyridin-6-yl)benzyl)-2,5-diazabicyclo[2.2.2]octane-2-carboxylate
• Step 3 3-((lR,4R)-5-(4-(l,4-Dimethyl-2-(4-(methylsulfonyl)phenyl)-lH-pyrrolo[3,2-c] pyridin-6-yl)benzyl)-2,5-diazabicyclo[2.2.2]octan-2-yl)-2,2-dimethylpropan-l-ol
• Step 7 methyl 6-chloro-l-methyl-2-(4-(methylsulfonyl)phenyl)-lH-pyrrolo[3,2-c] pyridine-4-carboxylate
• Step 5 4-[6-chl oro-1 -methyl-2-(4-methylsulfonylphenyl)pyrrolo[3,2-c]pyridin-4-yl] morpholine
• the resulting mixture was degassed three times with nitrogen and then stirred at 90 °C under nitrogen. After 2 h, the mixture was cooled to room temperature and purified by reverse flash chromatography with the following conditions: column, C18 silica gel; mobile phase, ACN and water (0.05% TFA), 10% ACN to 70% ACN gradient in 20 min; detector, UV 254 nm.
• the product was purified by Prep-HPLC (Column: X Bridge Prep Cl 8 OBD Column, 19*150 mm, 5 pm; Mobile Phase A: water (10 mmol/L NH4HCO3), Mobile Phase B: ACN; Flow rate: 20 mL/min; Gradient: 50% B to 65% B in
• the reaction mixture was then diluted with saturated sodium bicarbonate solution and extracted with DCM (3 x 50 mL). The combined organic layers were dried over Na2SO4 and concentrated under reduced pressure.
• the crude product was purified by Prep-HPLC (Column: Kinetex EVO C18 Column, 21.2*150, 5um; Mobile Phase A: water (10 mmol/L NH4HCO3), Mobile Phase B: ACN; Flow rate: 20 mL/min; Gradient: 40% B to 60% B in 5.5 min, 60% B; Wave Length: 254/210 nm;) to afford the title compound (8.6 mg, 11.6 % yield) as an off-white solid.
• the pharmacological properties of the compounds of this invention may be confirmed by a number of biological assays.
• the exemplified biological assays, which follow, have been carried out with compounds of the invention.
• HEK-BlueTM-cells (Invivogen) overexpressing human TLR7, TLR8 or TLR9 receptors were used for screening inhibitors of these receptors using an inducible SEAP (secreted embryonic alkaline phosphatase) reporter gene under the control of the IFN-P minimal promoter fused to five NF-KB and AP-1 -binding sites. Briefly, cells are seeded into Greiner 384 well plates (15000 cells per well for TLR7, 20,000 for TLR8 and 25,000 for TLR9) and then treated with test compounds in DMSO to yield a final dose response concentration range of 0.05 nM-50 pM.
• SEAP secreted embryonic alkaline phosphatase
• the cells are then stimulated with a TLR7 ligand (gardiquimod at a final concentration of 7.5 pM), TLR8 ligand (R848 at a final concentration of 15.9 pM) or TLR9 ligand (ODN2006 at a final concentration of 5 nM) to activate NF-KB and AP-1 which induce the production of SEAP.
• TLR7 ligand gardiquimod at a final concentration of 7.5 pM
• TLR8 ligand R848 at a final concentration of 15.9 pM
• ODN2006 TLR9 ligand
• SEAP levels are determined with the addition of HEK-BlueTM Detection reagent (Invivogen), a cell culture medium that allows for detection of SEAP, according to manufacturer’s specifications. The percent inhibition is determined as the % reduction in the HEK-Blue signal present in wells treated with agonist plus DMSO alone compared to wells treated with a known inhibitor.

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