WO2014078323A1 - N-pyrrolidinyl, n'-pyrazolyl- urea, thiourea, guanidine and cyanoguanidine compounds as trka kinase inhibitors - Google Patents
N-pyrrolidinyl, n'-pyrazolyl- urea, thiourea, guanidine and cyanoguanidine compounds as trka kinase inhibitors Download PDFInfo
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- WO2014078323A1 WO2014078323A1 PCT/US2013/069729 US2013069729W WO2014078323A1 WO 2014078323 A1 WO2014078323 A1 WO 2014078323A1 US 2013069729 W US2013069729 W US 2013069729W WO 2014078323 A1 WO2014078323 A1 WO 2014078323A1
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- alkyl
- formula
- compound
- alkoxy
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Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
-
- 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
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/415—1,2-Diazoles
- A61K31/4155—1,2-Diazoles non condensed and containing further heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C403/00—Derivatives of cyclohexane or of a cyclohexene or of cyclohexadiene, having a side-chain containing an acyclic unsaturated part of at least four carbon atoms, this part being directly attached to the cyclohexane or cyclohexene or cyclohexadiene rings, e.g. vitamin A, beta-carotene, beta-ionone
- C07C403/14—Derivatives of cyclohexane or of a cyclohexene or of cyclohexadiene, having a side-chain containing an acyclic unsaturated part of at least four carbon atoms, this part being directly attached to the cyclohexane or cyclohexene or cyclohexadiene rings, e.g. vitamin A, beta-carotene, beta-ionone having side-chains substituted by doubly-bound oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings
Definitions
- the present invention relates to novel compounds, to pharmaceutical compositions comprising the compounds, to processes for making the compounds and to the use of the compounds in therapy. More particularly, it relates to pyrrolidinyl urea, thiourea, guanidine and cyanoguanidine compounds which exhibit TrkA kinase inhibition, and which are useful in the treatment of pain, cancer, inflammation/inflammatory diseases, neurodegenerative diseases, certain infectious diseases, Sjogren's syndrome, endometriosis, diabetic peripheral neuropathy, prostatitis or pelvic pain syndrome.
- the current treatment regimens for pain conditions utilize several classes of compounds.
- the opioids such as morphine
- Nonsteroidal anti-inflammatory analgesics NSAIDs, such as COX-1 or COX-2 types
- COX-1 inhibitors can cause ulcers of the mucosa. Accordingly, there is a continuing need for new and more effective treatments for the relief of pain, especially chronic pain.
- Trk's are the high affinity receptor tyrosine kinases activated by a group of soluble growth factors called neurotrophins (NT).
- the Trk receptor family has three members: TrkA, TrkB and TrkC.
- the neurotrophins are (i) nerve growth factor (NGF) which activates TrkA, (ii) brain-derived neurotrophic factor (BDNF) and NT-4/5 which activate TrkB and (iii) NT3 which activates TrkC.
- NGF nerve growth factor
- BDNF brain-derived neurotrophic factor
- Trk-3 which activates TrkC.
- Trk's are widely expressed in neuronal tissue and are implicated in the maintenance, signaling and survival of neuronal cells (Patapoutian, A. et al., Current Opinion in Neurobiology, 2001, 11, 272-280).
- Inhibitors of the Trk/neurotrophin pathway have been demonstrated to be effective in numerous pre-clinical animal models of pain.
- antagonistic NGF and TrkA antibodies such as RN-624 have been shown to be efficacious in inflammatory and neuropathic pain animal models (Woolf, C.J. et al. (1994) Neuroscience 62, 327-331; Zahn, P.K. et al. (2004) J. Pain 5, 157-163; McMahon, S.B. et al., (1995) Nat. Med. 1, 774-780; Ma, Q. P. and Woolf, C. J. (1997) NeuroReport 8, 807-810; Shelton, D. L. et al.
- TrkA kinase may serve as a mediator of NGF driven biological responses, inhibitors of TrkA and/or other Trk kinases may provide an effective treatment for chronic pain states.
- Trk kinases are associated with many cancers including neuroblastoma (Brodeur, G. M., Nat. Rev. Cancer 2003, 3, 203-216), ovarian (Davidson. B., et al., Clin. Cancer Res. 2003, 9, 2248-2259), colorectal cancer (Bardelli, A., Science 2003, 300, 949), melanoma (Truzzi, F., et al., Dermato-Endocrinology 2008, 3 (1), pp. 32-36), head and neck cancer (Yilmaz, T., et al., Cancer Biology and Therapy 2010, 10 (6), pp.
- inhibition of the neurotrophin/Trk pathway has been shown to be effective in treatment of pre-clinical models of inflammatory diseases with NGF antibodies or non-selective small molecule inhibitors of TrkA.
- inhibition of the neurotrophin/Trk pathway has been implicated in preclinical models of inflammatory lung diseases including asthma (Freund-Michel, V; Frossard, N., Pharmacology & Therapeutics (2008) 117(1), 52-76), interstitial cystitis (Hu Vivian Y; et. al. The Journal of Urology (2005), 173(3), 1016-21), bladder pain syndrome (Liu, H.-T., et al, (2010) BJU International, 106 (1 1), pp.
- inflammatory bowel diseases including ulcerative colitis and Crohn's disease (Di Mola, F. F, et. al., Gut (2000) 46(5), 670-678) and inflammatory skin diseases such as atopic dermatitis (Dou, Y.-C, et. al. Archives of Dermatological Research (2006) 298(1), 31-37), eczema and psoriasis (Raychaudhuri, S. P., et al., J Investigative Dermatology (2004) 122(3), 812-819).
- TrkA receptor is also thought to be critical to the disease process of the parasitic infection of Trypanosoma cruzi (Chagas disease) in human hosts (de Melo- Jorge, M. et al., Cell Host & Microbe (2007) 1(4), 251-261).
- Trk inhibitors may also find use in treating disease related to an imbalance of the regulation of bone remodeling, such as osteoporosis, rheumatoid arthritis, and bone metastases.
- Bone metastases are a frequent complication of cancer, occurring in up to 70 percent of patients with advanced breast or prostate cancer and in approximately 15 to 30 percent of patients with carcinoma of the lung, colon, stomach, bladder, uterus, rectum, thyroid, or kidney.
- Osteolytic metastases can cause severe pain, pathologic fractures, life- threatening hypercalcemia, spinal cord compression, and other nerve-compression syndromes. For these reasons, bone metastasis is a serious and costly complication of cancer.
- TrkA receptors have been observed in the bone-forming area in mouse models of bone fracture (K. Asaumi, et al., Bone (2000) 26(6) 625-633). In addition, localization of NGF was observed in almost all bone-forming cells (K. Asaumi, et al.). Recently, it was demonstrated that a Trk inhibitor inhibits the signaling activated by neurotrophins binding to all three of the Trk receptors in human hFOB osteoblasts (J. Pinski, et al., (2002) 62, 986-989). These data support the rationale for the use of Trk inhibitors for the treatment of bone remodeling diseases, such as bone metastases in cancer patients.
- Trk inhibitors may also find use in treating diseases and disorders such as
- Trk kinases Several classes of small molecule inhibitors of Trk kinases said to be useful for treating pain or cancer are known (Expert Opin. Ther. Patents (2009) 19(3), 305-319).
- ring B is an aromatic ring
- ring D is an aromatic ring
- L is NR 3
- pyrrolidinyl urea, thiourea, guanidine and cyanoguanidine compounds are inhibitors of TrkA, and useful for treating disorders and diseases such as pain, including chronic and acute pain.
- Compounds of the invention useful in the treatment of multiple types of pain including inflammatory pain, neuropathic pain, and pain associated with cancer, surgery, or bone fracture.
- compounds of the invention are useful for treating cancer, inflammation or inflammatory diseases, neurodegenerative diseases, certain infectious diseases, Sjogren's syndrome, endometriosis, diabetic peripheral neuropathy, prostatitis or pelvic pain syndrome, and diseases related to an imbalance of the regulation of bone remodeling, such as osteoporosis, rheumatoid arthritis, and bone metastases.
- Another aspect of the present invention provides methods of treating a disease or disorder modulated by TrkA, comprising administering to a mammal in need of such treatment an effective amount of a compound of this invention or a stereoisomer, solvate or pharmaceutically acceptable salt thereof.
- the disease and disorders include chronic and acute pain, including but not limited to inflammatory pain, neuropathic pain, and pain associated with cancer, surgery, or bone fracture.
- the disease and disorders include, but are not limited to, cancer, inflammation or inflammatory diseases, neurodegenerative diseases, certain infectious diseases, Sjogren's syndrome, endometriosis, diabetic peripheral neuropathy, prostatitis or pelvic pain syndrome, and diseases related to an imbalance of the regulation of bone remodeling, such as osteoporosis, rheumatoid arthritis, and bone metastases.
- the treatment includes treating the mammal with a compound of this invention in combination with an additional therapeutic agent.
- Another aspect of the present invention provides a pharmaceutical composition comprising a compound of the present invention or a pharmaceutically acceptable salt thereof.
- Another aspect of the present invention provides the compounds of the present invention for use in therapy.
- Another aspect of the present invention provides the compounds of the present invention for use in the treatment of disease and disorders such as chronic and acute pain, including but not limited to inflammatory pain, neuropathic pain, and pain associated with cancer, surgery, or bone fracture.
- Another aspect of the present invention provides the compounds of the present invention for use in the treatment of disease and disorders selected from cancer, inflammation or inflammatory diseases, neurodegenerative diseases, certain infectious diseases, Sjogren's syndrome, endometriosis, diabetic peripheral neuropathy, prostatitis or pelvic pain syndrome, and diseases related to an imbalance of the regulation of bone remodeling, such as osteoporosis, rheumatoid arthritis, and bone metastases.
- Another aspect of the present invention provides the use of a compound of this invention in the manufacture of a medicament for the treatment of disease and disorders such as chronic and acute pain including, but not limited to, inflammatory pain, neuropathic pain, and pain associated with cancer, surgery, or bone fracture.
- Another aspect of the present invention provides the use of a compound of this invention in the manufacture of a medicament for the treatment of disease and disorders selected from cancer, inflammation or inflammatory diseases, neurodegenerative diseases, certain infectious diseases, Sjogren's syndrome, endometriosis, diabetic peripheral neuropathy, prostatitis or pelvic pain syndrome, and diseases related to an imbalance of the regulation of bone remodeling, such as osteoporosis, rheumatoid arthritis, and bone metastases.
- Another aspect of the present invention provides intermediates for preparing compounds of Formula I.
- Another aspect of the present invention includes methods of preparing, methods of separation, and methods of purification of the compounds of this invention.
- a representative compound of the invention (See Table B below), was found to be highly selective for TrkA over a panel of about 230 other kinases at 10 ⁇ concentration.
- compounds of the invention such as those shown in Table A below, were found to be at least 1000 fold more selective for TrkA versus p38a.
- One embodiment provides a com ound of Formula I:
- R a , R b , R c and R d are independently selected from H and (l-3C)alkyl, [0031] or R° and R d are independently selected from H and (l-3C)alkyl, and R a and
- R b together with the atom to which they are attached form a cyclopropyl ring
- X is O, S, NH, or N-CN
- R 1 is (1-3C alkoxy)(l-6C)alkyl, (trifluoromethoxy)(l -6C)alkyl, (1-3C sulfanyl)(l-6C)alkyl, monofluoro(l-6C)alkyl, difluoro(l-6C)alkyl, trifluoro(l-6C)alkyl, tetrafluoro(2-6C)alkyl, pentafluro(2-6C)alkyl, cyano(l-6C)alkyl, aminocarbonyl(l-6C)alkyl, hydroxy(l-6C)alkyl, dihydroxy(2-6C)alkyl, (l-6C)alkyl, (l-3Calkylamino)(l-3C)alkyl, (1- 4C alkoxycarbonyl)(l-6C)alkyl, amino(l-6C)alkyl, hydroxy(l-3C alkoxy)(l-6C)alkyl, di(
- R 2 is H, F, or OH
- Ring B is Ar 1 or hetAr 1 ;
- Ar 1 is phenyl optionally substituted with one or more substituents independently selected from halogen, CF 3 , CF 3 0-, (l-4C)alkoxy, hydroxy(l-4C)alkyl, (1- 6C)alkyl and CN;
- hetAr 1 is a 5-6 membered heteroaryl having 1-3 ring heteroatoms independently selected from N, S and O, and optionally substituted with one or more substituents independently selected from (l-6C)alkyl, halogen, OH, CF 3 , NH 2 and hydroxy(l- 2C)alkyl;
- Ring C is
- R 3 is H, (l-6C)alkyl, hydroxy(l-6C)alkyl, Ar 2 , hetCyc 1 , (3-7C)cycloalkyl, hetAr 2 , or a C5-C8 bridged carbocyclic ring;
- Ar 2 is phenyl optionally substituted with one or more substituents independently selected from halogen and (l-6C)alkyl;
- hetCyc 1 is a 5-6-membered saturated or partially unsaturated heterocyclic ring having 1-2 ring heteroatoms independently selected from N and O;
- hetAr is a 5-6 membered heteroaryl ring having 1-3 ring heteroatoms independently selected from N, O and S and optionally substituted with one or more substituents independently selected from (l-6C)alkyl and halogen;
- R 4 is selected from (1-6C alkyl)S0 2 -, (1-6C alkyl)C(O)- and from the structures:
- R m is (l-3C)alkyl substituted with 1-3 fluoros, or (3-4C)cycloalkyl;
- R n is (l-3C)alkyl
- R q is (1 -3C)alkyl optionally substituted with 1 -3 fluoros
- R x is (l-6C)alkyl, halogen, CN, hydroxy(l-6C)alkyl, trifluoro(l -6C)alkyl, (3-
- n 0, 1, 2, 3 or 4;
- m 0, 1, 2 or 3;
- R y is F or (l-3C)alkyl optionally substituted with 1-3 fluoros;
- p is 0, 1 or 2;
- R z is (3-4C)cycloalkyl, or (l-3C)alkyl optionally substituted with 1-3 fluoros;
- R 5 is H, ( 1 -6C)alkyl, monofluoro( 1 -6C)alkyl, difluoro( 1 -6C)alkyl, trifluoro( 1 -
- (l-6C)alkyl refers to saturated linear monovalent hydrocarbon radicals of one to six carbon atoms, one to four carbon atoms, and one to three carbon atoms, respectively, or a branched saturated monovalent hydrocarbon radical of three to six carbon atoms, three to four carbon atoms, or three carbon atoms, respectively.
- Examples include, but are not limited to, methyl, ethyl, 1- propyl, 2-propyl, 1 -butyl, 2 -methyl- 1 -propyl, 2-butyl, 2-methyl-2 -propyl, 2,2-dimethylpropyl, 1-pentyl, 2-pentyl, 3-pentyl, 2-methyl-2-butyl, 3-methyl-2-butyl, 3-methyl-l -butyl, 2-methyl- 1 -butyl, 1-hexyl, 2-hexyl, 3-hexyl, 2-methyl-2-pentyl, 3-methyl-2-pentyl, 4-methyl-2-pentyl, 3-methyl-3-pentyl, 2-methyl-3-pentyl, 2,3 -dimethyl -2 -butyl, and 3,3-dimethyl-2-butyl.
- (l-6C)Alkylsulfanyl refers to a (1-6C alkyl)S- group, wherein the radical is on the sulfur atom and the (1-6C alkyl) portion is as defined above. Examples include methylsulfanyl (CH 3 S-) and ethylsulfanyl (CH 2 CH 2 S-).
- (l-4C)Alkoxy refers to an -OR radical where R is (l-4C)alkyl, (l-3C)alkyl, (l-6C)alkyl, or (2-6C)alkyl, respectively, as defined above. Examples include methoxy, ethoxy, and the like.
- (1-4C Alkoxycarbonyl)(l-6C)alkyl means a (l-6C)alkyl group as defined herein, wherein one of the carbons is substituted with a (1-4C alkoxy)carbonyl group as defined herein.
- (1-3C Alkoxy)trifluoro(l-6C)alkyl means a (l-6C)alkyl group as defined herein, wherein one of the carbons is substituted with three fluoros, and another carbon is substituted with a (l-3C)alkoxy group as defined herein.
- (1-4C Alkoxycarbonyl)(l-3C alkoxy)(l-6C)alkyl means a (1-3C alkoxy)(l-
- Amino means a -NRR' group where R and R' are independently selected from hydrogen or (l-3C)alkyl as defined herein. Examples include H 2 N-, CH 3 NH-, (CH 3 ) 2 N, and the like.
- Amino(l-6C)alkyl means a linear saturated monovalent hydrocarbon radical of one to six carbon atoms or a branched saturated monovalent hydrocarbon radical of three to six carbon atoms, wherein one of the carbon atoms is substituted with one -NRR' group where R and R' are independently selected from hydrogen or (l-3C)alkyl as defined herein. Examples include aminomethyl, methylaminoethyl, 2-ethylamino-2-methylethyl, and the like.
- Aminocarbonyl means a RR'NCO- radical where R and R' are independently hydrogen or (l-6C)alkyl as defined herein. Examples include H 2 NCO, dimethylaminocarbonyl, and the like.
- Aminocarbonyl(l-6C)alkyl means a linear saturated hydrocarbon radical of one to six carbon atoms or a branched saturated monovalent hydrocarbon radical of three to six carbons wherein one of the carbon atoms is substituted with one aminocarbonyl group as defined herein, e.g., 2-aminocarbonylethyl, 1-, 2-, or 3-dimethylaminocarbonylpropyl, and the like.
- Cyano(l-6C)alkyl means a linear saturated hydrocarbon radical of one to six carbon atoms or a branched saturated monovalent hydrocarbon radical of three to six carbons substituted with a cyano (CN) group.
- (3-6C)Cycloalkyl means a cyclic saturated monovalent hydrocarbon radical of three to six carbon atoms, e.g., cyclopropyl, cyclobutyl, cyclopentyl, or cyclohexyl.
- Di(l-3C alkoxy)(l-6C)alkyl means a (l-6C)alkyl group as defined herein, wherein two carbons are each substituted with one (l-3C)alkoxy group as defined herein.
- Dihydroxy(2-6C)alkyl means a linear saturated hydrocarbon radical of two to six carbon atoms or a branched saturated monovalent hydrocarbon radical of three to six carbons substituted with two hydroxy (OH) groups, provided that two hydroxy groups are not both on the same carbon atom.
- Halogen as used herein means F, CI, Br or I.
- Heterocycle refers to a saturated or partially unsaturated ring system having one or more ring heteroatoms as recited for the specific heterocyclic group, wherein the heterocycle is optionally substituted with substituents as defined for that particular heterocyclic group.
- Heteroaryl refers to a 5-6 membered unsaturated ring system having one or more ring heteroatoms as recited for the specific heteroaryl group, wherein the heteroaryl is optionally substituted with substituents as defined for that particular heteroaryl group.
- Hydrocarbon radical of one to six carbon atoms or one to four carbon atoms, respectively, or a branched saturated monovalent hydrocarbon radical of three to six carbon atoms or three to four carbon atoms, respectively, wherein one of the carbon atoms is substituted with a hydroxy (OH) group.
- Hydroxy(l-3C alkoxy)(l-6C)alkyl means a (1-3C alkoxy)(l-6C)alkyl group as defined herein, wherein one of the carbons is substituted with a hydroxy group.
- Tetrafluoro(2-6C)alkyl and "pentafluoro(2-6C)alkyl” refer to a linear saturated monovalent hydrocarbon radical of two to six carbon atoms or a branched saturated monovalent hydrocarbon radical of three to six carbon atoms wherein four to five hydrogen atoms, respectively, is replaced by a fluoro group.
- (Trifluoromethoxy)(l-6C)alkyl means a linear saturated hydrocarbon radical of one to six carbon atoms substituted with one CF3O- group.
- Trifluoro(l-3C)alkoxy means a (l-3C)alkoxy group as defined herein, wherein one of the carbon atoms is substituted with three fluoros.
- (1-3C Sulfanyl)(l-6C)alkyl means a linear saturated hydrocarbon radical of one to six carbon atoms substituted with one (1-3C)S- group.
- compounds of the invention may contain groups that may exist in tautomeric forms, such as heteroatom substituted heteroaryl or heterocyclic groups and the like, which are illustrated in the following general and specific examples:
- R a , R b , R c and R d are independently selected from H and methyl.
- R a , R b , R c and R d are hydrogen.
- R a is methyl and R b , R c and R d are hydrogen.
- R a and R b are methyl and R c and R d are hydrogen.
- R a , R b and R c are hydrogen and R d is methyl.
- R a and R b are hydrogen and R c and R d are methyl.
- R° and R d are independently selected from H and (1- 3C)alkyl, and R a and R b together with the atom to which they are attached form a cyclopropyl ring.
- X is O.
- X is S.
- X is NH
- X is N-CN.
- R 1 is (1-3C alkoxy)(l-6C)alkyl, for example, methoxyethyl, methoxypropyl, ethoxyethyl and 2-methoxypropyl. Particular examples include 2-methoxyethyl and 2-methoxypropyl having the structures: [0091] In one embodiment, R 1 is 2-methoxyethyl.
- R 1 is (trifluoromethoxy)(l-6C)alkyl, for example,
- R 1 is (trifluoromethoxy)ethy 1.
- R 1 is (1-3C sulfanyl)(l-6C)alkyl, for example methylsulfanylethyl, ethylsulfanylethyl, and the like. In one embodiment, R 1 is methylsulfanylethyl.
- R 1 is monofiuoro(l-6C)alkyl, difluoro(l-6C)alkyl or trifluoro(l-6C)alkyl.
- R 1 is l,3-difluoroprop-2-yl, 2,2-difluoroethyl, 4,4,4-trifluorobutyl or 2,2,2-trifluoroethyl having the structures:
- R 1 is tetrafluoro(2-6C)alkyl or pentafluoro(2-6C)alkyl. In one embodiment, R 1 is 3,3,4,4,4-pentafluorobutyl.
- R 1 is cyano(l-6C)alkyl. In one embodiment, R 1 is 2- cyanoethyl.
- R 1 is hydroxy(l-6C)alkyl. In one embodiment, R 1 is 2- hydroxyethyl or 2-hydroxypropyl.
- R 1 is dihydroxy(2-6C)alkyl. In one embodiment, R 1 is the structure:
- R 1 is (l-6C)alkyl. In one embodiment, R 1 is methyl, ethyl, or propyl.
- R 1 is (1-3C alkylamino)(l-3C)alkyl, that is, a (l-3C)alkyl group which is substituted with a (1-3C alkyl)amino group, for example a (1-3C alkyl)NH- group such as methylamino.
- R 1 is (2-methylamino)ethyl.
- R 1 is (1-4C alkoxycarbonyl)(l-6C)alkyl. In one embodiment, R 1 is methoxycarbonylmethyl, having the structure: o
- R 1 is amino(l-6C)alkyl, such as methylamino(l-6C)alkyI. In one embodiment, R 1 is 2-methylaminoethyl.
- R 1 is hydroxy(l-3C alkoxy)(l-6C)alkyl. Examples include hydroxymethoxy(l-6C)alkyl. In one embodiment, R 1 is selected from the structures:
- R 1 is di(l-3C alkoxy)(l-6C)alkyl. Examples include dimethoxy(l-6C)alkyl. In one embodiment, R 1 is l,3-dimethoxyprop-2-yl having the structure:
- R 1 is (1-3C alkoxy)trifluoro(l-6C)alkyl. Examples include methoxytrifluoro(l-6C)alkyl. In one embodiment, R 1 is 3,3,3-trifluoro-2- methoxypropyl.
- R 1 is hydroxytrifluoro(l-6C)alkyl. In one embodiment, R 1 is 3,3,3-trifluoro-2-hydroxypropyl.
- R 1 is (1-4C alkoxycarbonyl)(l-3C alkoxy)(l-6C)alkyl. Examples include (methoxycarbonyl)methoxy(l-6C)alkyl.
- R 1 is a group having the structure:
- R 1 is hydroxycarbonyl(l-3C alkoxy)(l-6C)alkyl. Examples include (methoxycarbonyl)hydroxy(l-6C)alkyl. In one embodiment, R 1 is a group having the structure:
- R 1 is selected from (1-3C alkoxy)(l-6C)alkyl, difiuoro(l- 6C)alkyl and trifluoro(l-6C)alkyl.
- R 2 is H.
- R 2 is F. [00113] In one embodiment, R 2 is OH.
- Ring B is is Ar 1 , where Ar 1 is phenyl optionally substituted with one or more substituents independently selected from halogen, CF 3 , CF 3 0-, (l-4C)alkoxy, hydroxy(l-4C)alkyl, (l-6C)alkyl, and CN. In one embodiment, Ar 1 is phenyl optionally substituted with one or more substituents independently selected from halogen, CF 3 , (l-4C)alkoxy and CN. In one embodiment, Ar 1 is phenyl optionally substituted with one or more substituents independently selected from F, CI, CF 3 , MeO and CN.
- Ring B when represented by Ar 1 is selected from phenyl, 2-fluorophenyl, 3 -fluorophenyl, 4-fluorophenyl, 3,4-difluorophenyl, 3,5- difluorophenyl, 2,4-difluorophenyl, 2,5-difluorophenyl, 3,4,5-trifluorophenyl, 2- chlorophenyl, 3-chlorophenyl, 4-chlorophenyl, 3-trifiuoromethylphenyl 3-methoxyphenyl, 3- chloro-4-fluorophenyl, 4-chloro-3 -fluorophenyl, 3-chloro-5-fluorophenyl, 3-cyano-5- fluorophenyl, 2-cyanophenyl, 4-cyanophenyl and 3-cyano-4-fluorophenyl.
- Ring B is is Ar 1 , wherein Ar 1 is phenyl optionally substituted with one or more halogens. In one embodiment, Ar 1 is phenyl optionally substituted with one or more F or CI. In one embodiment, Ar 1 is 3 -fluorophenyl, 4- fluorophenyl, 3,4-difluorophenyl, 3,5-difluorophenyl, 3,4,5-trifluorophenyl, 3-chlorophenyl, 3-chloro-4-fluorophenyl, 3-chloro-5-fluorophenyl, or 4-chloro-3 -fluorophenyl.
- Ring B is hetAr 1 , where hetAr 1 is a 5-6 membered heteroaryl having 1-3 ring heteroatoms independently selected from N, S and O, and is optionally substituted with one or more substituents independently selected from (1- 6C)alkyl, halogen, OH, CF 3 , NH 2 and hydroxy(l-2C)alkyl.
- Ring B is hetAr 1 , wherein hetAr 1 is a 5-6 membered heteroaryl having 1-2 ring heteroatoms independently selected from N, S and O, and optionally substituted with 1-2 groups independently selected from (l-6C)alkyl, halogen, OH, CF 3 , NH 2 and hydroxy(l-2C)alkyl.
- Ring B include pyridyl, thiophenyl, thiazolyl, oxazolyl, and isoxazolyl rings optionally substituted with 1-2 groups independently selected from (l-6C)alkyl, halogen, OH, CF 3 , NH 2 and hydroxy(l-2C)alkyl.
- Ring B is a pyridyl, thiophenyl, thiazolyl, oxazolyl, or isoxazolyl ring optionally substituted with 1-2 groups independently selected from halogen and (l-6C)alkyl.
- Ring B when represented by hetAr 1 is selected from pyrid-4-yl, pyrid-3-yl, pyrid-2-yl, 5-fiuoropyrid-3-yl, thien-2-yl, thiazol-2-yl, 2,4- dimethylthiazol-5-yl, oxazol-5-yl, isoxazol-5-yl, 5-chloropyrid-3-yl, 5-fluoropyrid-2-yl, 3- fluoropyrid-4-yl and 1 -methylpyrazol-4-yl having the structures:
- Ring B is a pyridyl ring optionally substituted with 1-2 groups independently selected from (l-6C)alkyl and halogen.
- R is H.
- R is (l-6C)alkyl. In one embodiment, R is methyl or ethyl.
- R is hydroxy(l-6C)alkyl. In one embodiment, R is 2- hydroxyethyl.
- R 3 is Ar 2 , where Ar 2 is phenyl optionally substituted with one or more substituents independently selected from halogen and (l-6C)alkyl.
- R 3 is phenyl, 2-fluorophenyl, 3-fluorophenyl, 4-fluorophenyl, 2-methylphenyl, 3-methylphenyl, 4-methylphenyl, 3-(hydroxymethyl)phenyl, 3-chlorophenyl, 3-chloro-4- fluorophenyl and 3-chloro-2-fluorophenyl.
- Particular examples of R when represented by Ar 2 include phenyl, 2-fluorophenyl, 3-fluorophenyl, 4-fluorophenyl, 2-methylphenyl, 3- methylphenyl and 4-methylphenyl.
- R 3 is phenyl
- R is hetCyc , where hetCyc is a 5-6-membered saturated or partially unsaturated heterocyclic ring having 1-2 ring heteroatoms independently selected from N and O.
- R is a pyrrolidinyl, tetrahydrofuranyl, imidazolidinyl, piperidinyl, piperazinyl, tetrahydropyranyl, or morpholinyl ring.
- R is tetrahydro-2H-pyran-4-y 1.
- R is (3-7C)cycloalkyl. In one embodiment R is cyclohexyl.
- R 3 is hetAr 2 , where hetAr 2 is 5-6 membered heteroaryl ring having 1-3 ring heteroatoms independently selected from N, O and S and optionally substituted with one or more substituents independently selected from (l-6C)alkyl and halogen.
- R 3 is a thienyl, furyl, imidazolyl, pyrazolyl, thiazolyl, isothiazolyl, oxazolyl, isoxazolyl, triazolyl, thiadiazolyl, oxadiazolyl, pyridyl, pyrimidyl, pyrazinyl, or pyridazinyl optionally substituted with one or more substituents independently selected from (l-6C)alkyl and halogen.
- R is pyrazolyl, pyridyl or pyridazinyl optionally substituted with one or more substituents independently selected from (l-6C)alkyl and halogen.
- R 3 is 1 -methyl- lH-pyrazol-4-yl, pyrid-2-yl, pyrid-3-yl, pyrid-4-yl, pyridazinyl or 3-chloropyrid-5-yl.
- R 3 is a C5-C8 bridged carbocyclic ring.
- An example includes the structure:
- R 3 is selected from Ar 2 , hetAr 2 and (l-6C)alkyl.
- R 3 is selected from Ar 2 and hetAr 2 .
- R 3 is selected from Ar 2 .
- R m , R q , R y , R z , and p are as defined for Formula I.
- R 4 is selected from (1-6C alkyl)S0 2 - and (1-
- R 4 is (1-6C alkyl)S0 2 -. In one embodiment, R 4 is CH 3 S0 2 -.
- R is selected from the structures:
- R m , R q , R y , R z , and p are as defined for Formula I.
- R 4 is [00141] where R m , R y and p are as defined for Formula I. In one embodiment, p is 0. In one embodiment, p is 1. In one embodiment, R 4 has the structure:
- R z , R y and p are as defined for Formula I.
- R z is (1- 3C)alkyl.
- R z is methyl.
- R z is (l-3C)alkyl substituted with 1-3 fluoros.
- R z is CF 3 .
- R z is cyclopropyl or cyclobutyl.
- p is 0.
- p is 1.
- R has the structure:
- R z , R y and p are as defined for Formula I.
- R z is (1- 3C)alkyl.
- R z is methyl.
- R z is (l-3C)alkyl substituted with 1-3 fluoros.
- R z is CF 3 .
- R z is cyclopropyl or cyclobutyl.
- p is 0. In one embodiment, p is 1.
- R 4 is
- R z , R y and p are as defined for Formula I.
- R z is (1- 3C)alkyl.
- R z is methyl.
- R z is (l-3C)alkyl substituted with 1-3 fluoros.
- R z is CF 3 .
- R z is cyclopropyl or cyclobutyl.
- p is 0. In one embodiment, p is 1.
- R z , R y and p are as defined for Formula I.
- R z is (1- 3C)alkyl.
- R z is methyl.
- R z is (l-3C)alkyl substituted with 1-3 fluoros.
- R z is CF 3 .
- R z is cyclopropyl or cyclobutyl.
- p is 0. In one embodiment, p is 1.
- R 4 is selected from the structures:
- R q , R y and p are as defined for Formula I.
- R q is (1- 3C)alkyl.
- R q is methyl.
- R q is (l-3C)alkyl substituted with 1-3 fluoros.
- R q is CF 3 .
- p is 0. In one embodiment, p is 1.
- R 4 is selected from the structures:
- R q , R y and p are as defined for Formula I.
- R q is (1- 3C)alkyl.
- R q is methyl.
- R q is (l-3C)alkyl substituted with 1-3 fluoros.
- R q is CF 3 .
- p is 0. In one embodiment, p is 1.
- R 4 is selected from the structures:
- R n , R q , R x , Ry, n and m are as defined for Formula I.
- R q is (l-3C)alkyl. In one embodiment, R q is methyl. In one embodiment, R q is (l-3C)alkyl substituted with 1-3 fluoros. In one embodiment, R q is
- R x is fluoro, methyl, ethyl, methoxy, ethoxy, cyano or cyclopropyl.
- n is 0 or 1.
- m is 0 or 1.
- R 4 is selected from the following structures:
- R 5 is H.
- R 5 is (l-6C)alkyl. In one embodiment, R 5 is methyl, ethyl, propyl, isopropyl or butyl. In one embodiment, R 5 is methyl.
- R 5 is monofluoro(l-6C)alkyl, difluoro(l-6C)alkyl, trifluoro(l-6C)alkyl, tetrafluro(2-6C)alkyl or pentafluro(2-6C)alkyl.
- R 5 is fluoromethyl, 2-fluoroethyl, difluoromethyl, 2,2-difluoroethyl, l,3-difluoroprop-2-yl, trifluoromethyl, 2,2,2-trifluoroethyl, 3,3,3-trifluoropropyl, 1 ,1,2,2-tetrafluoropropyl or 2,2,3,3,3-pentafluoropropyl.
- R 5 is halogen. In one embodiment, R 5 is F. In one embodiment, R 5 is CI. In one embodiment, R 5 is Br.
- R 5 is CN
- R 5 is (l-4C)alkoxy. In one embodiment, R 5 is methoxy or ethoxy.
- R 5 is hydroxy(l-4C)alkyl. In one embodiment, R 5 is hydroxymethyl or 3-hydroxypropyl.
- R 5 is (l-6C)alkylsulfanyl. In one embodiment, R 5 is methylsulfanyl (MeS-).
- R 5 is phenyl optionally substituted with one or more substituents independently selected from halogen, (l-6C)alkyl and (l-6C)alkoxy. In one embodiment, R 5 is phenyl optionally substituted with one or more substituents independently selected from F, CI, methyl, ethyl, methoxy and ethoxy. In one embodiment, R 5 is phenyl. [00171] In one embodiment, R 5 is (3-4C)cycloalkyl. In one embodiment, R 5 is cyclopropyl. In one embodiment, R 5 is cyclobutyl.
- R 5 is amino. In one embodiment, R 5 is NH 2 .
- R 5 is aminocarbonyl. In one embodiment, R 5 is
- R 5 is H, halogen, CN, (l-6C)alkyl, (l-4C)alkoxy, hydroxy(l-4C)alkyl, (l-6C)alkylsulfanyl, or phenyl optionally substituted with one or more substituents independently selected from halogen, (l-6C)alkyl and (l-6C)alkoxy.
- R 5 is H, halogen, CN, (l-6C)alkyl, (l-4C)alkoxy, hydroxy(l-4C)alkyl, or phenyl optionally substituted with one or more substituents independently selected from halogen, (l-6C)alkyl and (l-6C)alkoxy.
- R 5 is H, halogen, or (l-6C)alkyl.
- R 5 is H, methyl, CI or Br.
- Formula I comprises compounds wherein:
- R a , R b , R c and R d are H;
- R 1 is (1-3C alkoxy)(l-6C)alkyl
- R 2 is H
- Ring B is Ar 1 ;
- Ar 1 is phenyl optionally substituted with one or more substituents independently selected from halogen, CF 3 , CF 3 0-, (l-4C)alkoxy, hydroxy(l-4C)alkyl, (1- 6C)alkyl and CN;
- Ring C is
- R 3 is Ar 2 ;
- Ar 2 is phenyl optionally substituted with one or more substituents independently selected from halogen and (l-6C)alkyl;
- R 4 is selected from the structures:
- R m is (l-3C)alkyl substituted with 1-3 fluoros, or (3-4C)cycloalkyl;
- R n is (l-3C)alkyl
- R q is (1 -3C)alkyl optionally substituted with 1 -3 fluoros;
- R x is (l-6C)alkyl, halogen, CN, hydroxy(l-6C)alkyl, trifluoro(l-6C)alkyl, (3-
- n 0, 1, 2, 3 or 4;
- m 0, 1, 2 or 3;
- R y is F or (1 -3C)alkyl optionally substituted with 1 -3 fluoros;
- p is 0, 1 or 2;
- R z is (3-4C)cycloalkyl, or (l-3C)alkyl optionally substituted with 1-3 fluoros;
- R 5 is (l-6C)alkyl.
- Formula I comprises compounds wherein:
- R a , R b , R c and R d are H;
- X is O
- R 1 is (1-3C alkoxy)(l-6C)alkyl
- R 2 is H
- Ring B is Ar 1 ;
- Ar 1 is phenyl optionally substituted with one or more halogens
- R m is (l-3C)alkyl substituted with 1-3 fluoros, or (3-4C)cycloalkyl;
- R n is (l-3C)alkyl
- R q is (1 -3C)alkyl optionally substituted with 1 -3 fluoros
- R x is (l-6C)alkyl, halogen, CN, hydroxy(l-6C)alkyl, trifluoro(l-6C)alkyl, (3-
- n 0, 1, 2, 3 or 4;
- m 0, 1, 2 or 3;
- R y is F or (l-3C)alkyl optionally substituted with 1-3 fluoros;
- p is 0, 1 or 2;
- R z is (3-4C)cycloalkyl, or (l-3C)alkyl optionally substituted with 1-3 fluoros;
- R 5 is (l-6C)alkyl.
- R a , R b , R c and R d are independently selected from H and ( 1 -3C)alkyl
- R c and R d are independently selected from H and ( 1 -3C)alkyl and R a and R b together with the atom to which they are attached form a cyclopropyl ring.
- X is O, S, NH or N-CN;
- R 1 is (1-3C alkoxy)(l-6C)alkyl, (trifluoromethoxy)(l-6C)alkyl, (1-3C sulfanyl)(l-6C)alkyl, monofluoro(l-6C)alkyl, difluoro(l-6C)alkyl, trifluoro(l-6C)alkyl, tetrafluoro(2-6C)alkyl, pentafluro(2-6C)alkyl, cyano(l-6C)alkyl, aminocarbonyl(l-6C)alkyl, hydroxy(l-6C)alkyl, dihydroxy(2-6C)alkyl, (l-6C)alkyl, (l-3Calkylamino)(l-3C)alkyl, (1- 4C alkoxycarbonyl)(l-6C)alkyl, amino(l-6C)alkyl, hydroxy(l-3C alkoxy)(l-6C)alkyl, di(
- R 2 is H, F, or OH
- Ring B is Ar 1 or hetAr 1 ;
- Ar 1 is phenyl optionally substituted with one or more substituents independently selected from halogen, CF 3 , CF 3 0-, (l-4C)alkoxy, hydroxy(l-4C)alkyl, (1- 6C)alkyl and CN;
- hetAr 1 is a 5-6 membered heteroaryl having 1-3 ring heteroatoms independently selected from N, S and O, and optionally substituted with one or more substituents independently selected from (l-6C)alkyl, halogen, OH, CF 3 , NH 2 and hydroxy(l- 2C)alkyl;
- Ring C is formula C- 1
- R 3 is H, (l-6C)alkyl, hydroxy(l-6C)alkyl, Ar 2 , hetCyc 1 , (3-7C)cycloalkyl, hetAr 2 , or a C5-C8 bridged carbocyclic ring;
- Ar is phenyl optionally substituted with one or more substituents independently selected from halogen and (l-6C)alkyl;
- hetCyc 1 is a 5-6-membered saturated or partially unsaturated heterocyclic ring having 1-2 ring heteroatoms independently selected from N and O;
- hetAr is a 5-6 membered heteroaryl ring having 1-3 ring heteroatoms independently selected from N, O and S and optionally substituted with one or more substituents independently selected from (l-6C)alkyl and halogen;
- R 4 is selected from the structures:
- R m is (l-3C)alkyl substituted with 1-3 fluoros, or (3-4C)cycloalkyl;
- R q is (l-3C)alkyl optionally substituted with 1-3 fluoros
- R y is F or (l-3C)alkyl optionally substituted with 1-3 fluoros;
- p is 0, 1 or 2;
- R z is (3-4C)cycloalkyl, or (l-3C)alkyl optionally substituted with 1-3 fluoros;
- R 5 is H, (l-6C)alkyl, monofluoro(l-6C)alkyl, difluoro(l-6C)alkyl, trifluoro(l-
- R a , R b , R c and R d are H.
- X is O.
- R 1 is (1-3C alkoxy)(l-6C)alkyl.
- R 2 is H.
- Ring B is Ar 1 , where Ar 1 is phenyl optionally substituted with one or more substituents independently selected from halogen, CF 3 , CF3O-, (l-4C)alkoxy, hydroxy(l-4C)alkyl, (l-6C)alkyl and CN.
- R 3 is Ar 2 , where Ar 2 is phenyl optionally substituted with one or more substituents independently selected from halogen and (1- 6C)alkyl.
- R 5 is (1 -6C)alkyl.
- compounds of Formula IA include compounds wherein:
- R a , R b , R c and R d are H;
- X is O
- R 1 is ( 1 -3C alkoxy)( 1 -6C)alkyl
- R 2 is H
- Ring B is Ar 1 ;
- Ar 1 is phenyl optionally substituted with one or more substituents independently selected from halogen, CF 3 , CF 3 0-, (l-4C)alkoxy, hydroxy(l-4C)alkyl, (1- 6C)alkyl and CN;
- Ring C is
- R 3 is Ar 2 ;
- Ar 2 is phenyl optionally substituted with one or more substituents independently selected from halogen and (l-6C)alkyl;
- R 4 is selected from the structures:
- R m is (l-3C)alkyl substituted with 1-3 fluoros, or (3-4C)cycloalkyl;
- R q is (l-3C)alkyl optionally substituted with 1-3 fluoros
- R y is F or (l-3C)alkyl optionally substituted with 1-3 fluoros;
- p is 0, 1 or 2;
- R z is (3-4C)cycloalkyl, or (l-3C)alkyl optionally substituted with 1-3 fluoros;
- R 5 is (l-6C)alkyl.
- compounds of Formula IA include compounds wherein:
- R a , R b , R c and R d are H;
- X is O
- R 1 is (1-3C alkoxy)(l-6C)alkyl
- R 2 is H
- Ring B is Ar 1 ;
- Ar 1 is phenyl optionally substituted with one or more halogens
- Ring C is
- R is phenyl
- R is selected from the structures:
- R 5 is (l-6C)alkyl.
- R a , R b , R c and R d are independently selected from H and (1 -3C)alkyl
- R° and R d are independently selected from H and (l-3C)alkyl and R a and R b together with the atom to which they are attached form a cyclopropyl ring.
- X is O, S, NH or N-CN
- R 1 is (1-3C alkoxy)(l-6C)alkyl, (trifluoromethoxy)(l-6C)alkyl, (1-3C sulfanyl)(l-6C)alkyl, monofluoro(l-6C)alkyl, difluoro(l-6C)alkyl, trifluoro(l-6C)alkyl, tetrafluoro(2-6C)alkyl, pentafluro(2-6C)alkyl, cyano(l-6C)alkyl, aminocarbonyl(l-6C)alkyl, hydroxy(l-6C)alkyl, dihydroxy(2-6C)alkyl, (l-6C)alkyl, (l-3Calkylamino)(l-3C)alkyl, (1- 4C alkoxycarbonyl)(l-6C)alkyl, amino(l-6C)alkyl, hydroxy(l-3C alkoxy)(l-6C)alkyl, di(
- R 2 is H, F, or OH
- Ring B is Ar 1 or hetAr 1 ;
- Ar 1 is phenyl optionally substituted with one or more substituents independently selected from halogen, CF 3 , CF3O-, (l-4C)alkoxy, hydroxy(l-4C)alkyl, (1- 6C)alkyl and CN;
- hetAr 1 is a 5-6 membered heteroaryl having 1-3 ring heteroatoms independently selected from N, S and O, and optionally substituted with one or more substituents independently selected from (l-6C)alkyl, halogen, OH, CF 3 , NH 2 and hydroxy(l- 2C)alkyl;
- Ring C is
- R 3 is H, (l-6C)alkyl, hydroxy(l-6C)alkyl, Ar 2 , hetCyc 1 , (3-7C)cycloalkyl, hetAr , or a C5-C8 bridged carbocyclic ring;
- Ar is phenyl optionally substituted with one or more substituents independently selected from halogen and (l-6C)alkyl;
- hetCyc 1 is a 5-6-membered saturated or partially unsaturated heterocyclic ring having 1-2 ring heteroatoms independently selected from N and O;
- hetAr is a 5-6 membered heteroaryl ring having 1-3 ring heteroatoms independently selected from N, O and S and optionally substituted with one or more substituents independently selected from (l-6C)alkyl and halogen;
- 4 is selected from the structures:
- R n is (l-3C)alkyl
- R q is ( 1 -3C)alkyl optionally substituted with 1 -3 fluoros;
- R x is (l-6C)alkyl, halogen, CN, hydroxy(l-6C)alkyl, trifluoro(l-6C)alkyl, (3-
- n 0, 1, 2, 3 or 4;
- m 0, 1, 2 or 3;
- R y is F or (1 -3C)alkyl optionally substituted with 1 -3 fluoros;
- p is 0, 1 or 2;
- R a , R b , R c and R d are H.
- X is O.
- R 1 is ( 1 -3C alkoxy)( 1 -6C)alkyl.
- R 2 is H.
- Ring B is Ar 1 , where Ar 1 is phenyl optionally substituted with one or more substituents independently selected from halogen, CF 3 , CF3O-, (l-4C)alkoxy, hydroxy(l-4C)alkyl, (l-6C)alkyl and CN.
- R 3 is Ar 2 , where Ar 2 is phenyl optionally substituted with one or more substituents independently selected from halogen and (1- 6C)alkyl.
- R 5 is (l-6C)alkyl.
- R x is selected from halogen, (l-6C)alkyl, (l-6C)alkoxy, CN and cyclopropyl.
- n is 0 or 1.
- n is 0 or 1.
- compounds of Formula IB include compounds wherein:
- R a , R b , R c and R d are H;
- X is O
- R 1 is (1-3C alkoxy)(l-6C)alkyl
- R 2 is H
- Ring B is Ar 1 ;
- Ar 1 is phenyl optionally substituted with one or more substituents independently selected from halogen, CF 3 , CF 3 0-, (l-4C)alkoxy, hydroxy(l-4C)alkyl, (1- 6C)alkyl and CN;
- Ring C is
- Ar 2 is phenyl optionally substituted with one or more substituents independently selected from halogen and (l-6C)alkyl;
- R 4 is selected from the structures:
- R q is (l-3C)alkyl optionally substituted with 1-3 fluoros
- n 0, 1, 2, 3 or 4;
- m 0, 1, 2 or 3;
- R y is F or (l-3C)alkyl optionally substituted with 1-3 fluoros;
- p is 0, 1 or 2;
- R 5 is (l-6C)alkyl.
- compounds of Formula IB include compounds wherein:
- R a , R b , R c and R d are H;
- X is O
- R 1 is (1-3C alkoxy)(l-6C)alkyl
- R 2 is H
- Ring B is Ar 1 ;
- Ax 1 is phenyl optionally substituted with one or more halogens
- Ring C is
- R 3 is phenyl
- R is selected from the structures:
- R 5 is (l-6C)alkyl.
- compounds according to the invention may contain one or more centers of asymmetry and may therefore be prepared and isolated in a mixture of isomers such as a racemic mixture, or in an enantiomerically pure form.
- compounds of Formula I or their salts may be isolated in the form of solvates, and accordingly that any such solvate is included within the scope of the present invention.
- compounds of Formula I can exist in unsolvated as well as solvated forms with pharmaceutically acceptable solvents such as water, ethanol, and the like.
- the compounds of Formula I include pharmaceutically acceptable salts thereof.
- the compounds of Formula I also include other salts of such compounds which are not necessarily pharmaceutically acceptable salts, and which are useful as intermediates for preparing and/or purifying compounds of Formula I and/or for separating enantiomers of compounds of Formula I.
- Particular examples of salts include hydrochloride salts and trifluoroacetate salts.
- the compounds of Formula I include the free base form of compounds of Examples 1 -31 , or pharmaceutically acceptable salts thereof.
- the compounds of Formula I include the hydrochloride salts of compounds of Examples 1-31.
- the compounds of Formula I include the trifluoroacetate salts of compounds of Examples 1-31.
- composition is compatible chemically and/or toxicologically, with the other ingredients comprising a formulation, and/or the mammal being treated therewith.
- the present invention also provides a process for the preparation of a compound of Formula I or a salt thereof as defined herein, which comprises:
- L 1 is a leaving group, in the presence of a base
- L 4 is Br or OTf
- R 1 , R a , R b , C c , R d , R 2 , R 3 and R 5 are as defined for Formula I, provided that R 5 is not halogen, with a corresponding boronic ester or boronic acid having the formula:
- the base may be an amine base, such as triethylamine or diisopropylethylamine.
- Suitable solvents include dichloromethane, dichloroethane, THF,
- the base may be an amine base, such as triethylamine or diisopropylethylamine.
- Suitable solvents include dichloromethane, dichloroethane, THF,
- the leaving group may be, for example, phenoxy or 4- nitrophenoxy.
- the base may be an amine base, such as triethylamine or diisopropylethylamine. Suitable solvents include DMA, DMF and DCE. The reaction is conveniently performed at ambient temperature.
- the leaving group may be, for example, phenoxy or 4- nitrophenoxy.
- the base may be an amine base, such as triethylamine or diisopropylethylamine. Suitable solvents include DCE, DMA and DMF. The reaction is conveniently performed at ambient temperature.
- the base may be an amine base, such as triethylamine or diisopropylethylamine.
- Suitable solvents include toluene and DMF.
- the reaction is conveniently performed at elevated temperatures, for example the reflux temperature of the solvent.
- the base may be an amine base, such as triethylamine or diisopropylethylamine.
- Suitable solvents include DCM, DCE, DMF and THF. The reaction is conveniently performed at temperatures between about 0 °C and ambient temperature.
- a compound of Formula VII may be prepared by reacting a compound of Formula III with bis(trichloromethyl) carbonate in the presence of a base, such as an amine base.
- the base may be an amine base, such as triethylamine or diisopropylethylamine.
- Suitable solvents include DMF, DMA and THF.
- the reaction is conveniently performed at temperatures between ambient temperature and 60 °C.
- the reaction is conveniently performed in the presence of a ligand, such as PPh 3 or tricyclohexylphosphine.
- a ligand such as PPh 3 or tricyclohexylphosphine.
- Suitable palladium catalysts include Pd 2 dba 3 or Pd(PPh 3 ) 4 .
- Suitable bases include an alkali metal carbonate, such as sodium carbonate, potassium carbonate, cesium carbonate, or potassium phosphate.
- suitable solvents include dioxane, toluene, or DME.
- the reaction is conveniently performed at temperatures between 80-110 °C.
- Amine groups in compounds described in any of the above methods may be protected with any convenient amine protecting group, for example as described in Greene & Wuts, eds., "Protecting Groups in Organic Synthesis", 2 nd ed. New York; John Wiley & Sons, Inc., 1991.
- amine protecting groups include acyl and alkoxycarbonyl groups, such as t-butoxycarbonyl (BOC) and [2-(trimethylsilyl)ethoxy]methyl (SEM).
- carboxyl groups may be protected with any convenient carboxyl protecting group, for example as described in Greene & Wuts, eds., "Protecting Groups in Organic Synthesis", 2 nd ed.
- carboxyl protecting groups include (l-6C)alkyl groups, such as methyl, ethyl and t-butyl.
- Alcohol groups may be protected with any convenient alcohol protecting group, for example as described in Greene & Wuts, eds., "Protecting Groups in Organic Synthesis", 2 nd ed. New York; John Wiley & Sons, Inc., 1991.
- alcohol protecting groups include benzyl, trityl, silyl ethers, and the like.
- the compounds of the formulas II, III, III, IV, V, VI, VII and VIII are provided as further aspects of the invention.
- the compounds of the formulas II, III, III, IV, V, VI, VII and VIII are useful as intermediates for the synthesis of compounds of Formula I.
- a process for preparing enantiomer 1 of II-A comprises:
- Ring B and the NH 2 group are in the trans configuration; Ring B is Ar 1 or hetAr 1 ; Ar 1 is phenyl optionally substituted with one or more substituents independently selected from halogen, CF 3 , CF 3 0-, (l-4C)alkoxy, hydroxy(l-4C)alkyl, (l-6C)alkyl and CN; and hetAr 1 is a 5-6 membered heteroaryl having 1-3 ring heteroatoms independently selected from N, S and O, and optionally substituted with 1-2 groups independently selected from (1- 6C)alkyl, halogen, OH, CF 3 , NH 2 and hydroxy(l-2C)alkyl; said method comprising:
- R 1 is 2-methoxyethoxy and Ring B is 4-fluorophenyl
- racemic trans II-A is prepared by the process comprising:
- R 1 is 2-methoxyethoxy and Ring B is 3,4-difluorophenyl.
- the inorganic base is an alkali metal hydroxide such as sodium hydroxide.
- R 1 and Ring B are as defined herein.
- R 1 is 2-methoxyethoxy and Ring B is 4-fluorophenyl.
- R 1 is 2-methoxyethoxy and Ring B is 3,4-difluorophenyl.
- Compounds of Formula I are useful in the treatment of pain, cancer, inflammation/inflammatory diseases, neurodegenerative diseases, certain infectious diseases, Sjogren's syndrome, endometriosis, diabetic peripheral neuropathy, prostatitis or pelvic pain syndrome.
- compounds of Formula I are useful for treating pain, including chronic and acute pain.
- compounds of Formula I are useful in the treatment of multiple types of pain including inflammatory pain, neuropathic pain, and pain associated with cancer, surgery or bone fracture.
- compounds of Formula I are useful for treating acute pain.
- Acute pain as defined by the International Association for the Study of Pain, results from disease, inflammation, or injury to tissues. This type of pain generally comes on suddenly, for example, after trauma or surgery, and may be accompanied by anxiety or stress, and is confined to a given period of time and severity. In some instances, it can become chronic.
- compounds of Formula I are useful for treating chronic pain.
- Chronic pain as defined by the International Association for the Study of Pain, is widely believed to represent a disease in itself. It can be made much worse by environmental and psychological factors. Chronic pain persists over a longer period than acute pain and is resistant to most medical treatments, generally over 3 months or more. It can and often does cause severe problems for patients.
- Compounds of Formula I are also useful for treating cancer.
- Particular examples include neuroblastoma, ovarian, pancreatic, colorectal and prostate cancer.
- Compounds of Formula I are also useful for treating inflammation and certain infectious diseases.
- compounds of Formula I may be used to treat interstitial cystitis (IC), painful bladder syndrome (PBS), urinary incontinence, asthma, atopic dermatitis, and psoriasis.
- IC interstitial cystitis
- PBS painful bladder syndrome
- urinary incontinence asthma
- asthma atopic dermatitis
- psoriasis psoriasis
- Compounds of Formula I are also useful for treating a neurodegenerative disease in a mammal, comprising administering to said mammal one or more compounds of Formula I or a pharmaceutically acceptable salt thereof in an amount effective to treat said neurodegenerative disease.
- compounds of Formula I may also be used to treat demyelination and dysmyelination by promoting myelination, neuronal survival, and oligodendrocyte differentiation via blocking Sp35-TrkA interaction.
- the neurodegenerative disease is multiple sclerosis.
- the neurodegenerative disease is Parkinson's disease.
- the neurodegenerative disease is Alzheimer's disease.
- Compounds of Formula I are also useful for treating certain infectious diseases such as Trypanosoma cruzi infection in a mammal.
- Compounds of Formula I are also useful for treating Sjogren's syndrome in a mammal.
- Compounds of Formula I are also useful for treating endometriosis in a mammal.
- Compounds of Formula I are also useful for treating diabetic peripheral neuropathy in a mammal.
- Compounds of Formula I are also useful for treating prostatitis in a mammal.
- Compounds of Formula I are also useful for treating pelvic pain syndrome in a mammal.
- Compounds of Formula I are also useful in treating diseases related to an imbalance of the regulation of bone remodeling, such as osteoporosis, rheumatoid arthritis, and bone metastases.
- treat or “treatment” refer to therapeutic or palliative measures.
- Beneficial or desired clinical results include, but are not limited to, alleviation, in whole or in part, of symptoms associated with a disorder or condition, diminishment of extent of disease, stabilized (i.e., not worsening) state of disease, delay or slowing of disease progression, amelioration or palliation of the disease state, and remission (whether partial or total), whether detectable or undetectable.
- Treatment can also mean prolonging survival as compared to expected survival if not receiving treatment.
- compounds of Formula I are useful for preventing diseases and disorders as defined herein.
- the term "preventing” as used herein means the prevention of the onset, recurrence or spread, in whole or in part, of the disease or condition as described herein, or a symptom thereof, and includes to the administration of a compound of Formula I prior to the onset of symptoms.
- one embodiment of this invention provides a method of treating pain in a mammal, comprising administering to said mammal in need thereof one or more compounds of Formula I or a pharmaceutically acceptable salt thereof in an amount effective to treat said pain.
- the pain is chronic pain.
- the pain is acute pain.
- the pain is inflammatory pain, neuropathic pain, or pain associated with cancer, surgery, or bone fracture.
- Another embodiment of this invention provides a method of preventing pain in a mammal, comprising administering to said mammal in need thereof one or more compounds of Formula I or a pharmaceutically acceptable salt thereof in an amount effective to prevent said pain.
- the pain is chronic pain.
- the pain is acute pain.
- the pain is inflammatory pain, neuropathic pain, or pain associated with cancer, surgery, or bone fracture.
- Another embodiment of this invention provides a method of treating cancer in a mammal, comprising administering to said mammal in need thereof one or more compounds of Formula I or a pharmaceutically acceptable salt thereof in an amount effective to treat said cancer.
- a method for treating a patient diagnosed with a cancer having a dysregulation of TrkA comprising administering to the patient a therapeutically effective amount of a compound of the invention or a pharmaceutically acceptable salt thereof.
- the dysregulation of TrkA comprises overexpression of wild-type TrkA (autocrine activation).
- the dysregulation of TrkA comprises one or more chromosome translocations or inversions resulting in TrkA gene fusions.
- the dysregulation is a result of genetic translocations in which the expressed protein is a fusion protein containing residues from non-TrkA and TrkA proteins, and at a minimum the TrkA kinase domain.
- the TrkA fusion protein is LMNA- TrkA, TFG-TrkA, TPM3-TrkA, CD74-TrkA, NFASC-TrkA, MPRIP-TrkA, BCAN-TrkA, or TPR-TrkA, where:
- LMNA Prelamin-A/C; TFG TRK-fused gene protein;
- NFASC Neurofascin
- MPRIP MPRIP protein
- the dysregulation of TrkA comprises one or more deletions, insertions or mutations in the TrkA protein.
- the dysregulation comprises a deletion of one or more residues from the TrkA protein, resulting in constitutive activity of TrkA kinase.
- the deletion includes deletion of residues 303- 377 in TrkA Isoform 2.
- the dysregulation of TrkA comprises a splice variation in which the expressed protein is an alternatively spliced variant of TrkA having one or more residues deleted resulting in constitutive activity of TrkA kinase.
- an alternatively spliced form of TrkA with constitutive activity has deletions of exons 8, 9, and 11 resulting in an expressed protein missing residues 192-284 and 393-398 relative to TrkA Isoform 2.
- Radiotherapy e.g. radioiodide therapy, Lung Cancer Nature Medicine 19, external-beam radiation, radium 223
- chemotherapeutics as single agents (e.g. afatinib dimaleate, bevacizumab, carboplatin, cetuximab, cisplatin, crizotinib, erlotinib, gefitinib, gemcitabine, methotrexate, paclitaxel, pemetrexed) or combinations (e.g.
- TrkA comprises one or more deletions, insertions or mutations in the TrkA protein, including:
- chemotherapeutics 314 e.g. abiraterone, cabazitaxel,
- fluorouracil gemcitabine, mitomycin C
- combinations e.g. gemcitabine-oxaliplatin
- a method for treating a patient diagnosed with a cancer having a dysregulation of TrkA comprising administering to the patient a therapeutically effective amount of a compound of the invention, or a pharmaceutically acceptable salt thereof, wherein the cancer is selected from non-small cell lung cancer, papillary thyroid carcinoma, glioblastoma multiforme, acute myeloid leukemia, colorectal carcinoma, large cell neuroendocrine carcinoma, prostate cancer, neuroblastoma, pancreatic carcinoma, melanoma, head and neck squamous cell carcinoma and gastric carcinoma.
- the compounds of the present invention are useful for treating cancer in combination with one or more additional therapeutic agents or therapies that work by the same or a different mechanism of action.
- the additional therapeutic agent(s) is selected from receptor tyrosine kinase-targeted therapeutic agents, including cabozantinib, crizotinib, erlotinib, gefitinib, imatinib, lapatinib, nilotinib, pazopanib, pertuzumab, regorafenib, sunitinib, and trastuzumab.
- the additional therapeutic agent(s) is selected from signal transduction pathway inhibitors, including Ras-Raf-MEK-ERK pathway inhibitors (e.g.
- sorafenib, trametinib, vemurafenib), PI3K-Akt-mTOR-S6K pathway inhibitors e.g. everolimus, rapamycin, perifosine, temsirolimus
- modulators of the apoptosis pathway e.g. obataclax
- the additional therapeutic agent(s) is selected from cytotoxic chemotherapeutics, including arsenic trioxide, bleomycin, cabazitaxel, capecitabine, carboplatin, cisplatin, cyclophosphamide, cytarabine, dacarbazine, daunorubicin, docetaxel, doxorubicin, etoposide, fluorouracil, gemcitabine, irinotecan, lomustine, methotrexate, mitomycin C, oxaliplatin, paclitaxel, pemetrexed, temozolomide, and vincristine.
- cytotoxic chemotherapeutics including arsenic trioxide, bleomycin, cabazitaxel, capecitabine, carboplatin, cisplatin, cyclophosphamide, cytarabine, dacarbazine, daunorubicin, docetaxel,
- the additional therapeutic agent(s) is selected from angiogenesis-targeted therapies, including aflibercept and bevacizumab.
- the additional therapeutic agent(s) is selected from immune-targeted agents, including aldesleukin, ipilimumab, lambrolizumab, nivolumab, sipuleucel-T.
- the additional therapeutic agent(s) is selected from agents active against the TrkA pathway, including NGF-targeted biopharmaceuticals such as NGF antibodies, and panTrk inhibitors.
- the additional therapeutic agent or therapy is radiotherapy, including radioiodide therapy, external-beam radiation and radium 223 therapy.
- the additional therapeutic agent(s) includes any one of the above listed therapies or therapeutic agents which are standards of care in cancers wherein the cancer has a dysregulation of TrkA.
- a method of treating cancer in a patient comprising administering to said patient a compound of the invention or a pharmaceutically acceptable salt thereof, in combination with at least one additional therapy or therapeutic agent selected from radiotherapy (e.g. radioiodide therapy, external-beam radiation, radium 223 therapy), cytotoxic chemotherapeutics (e.g.
- arsenic trioxide bleomycin, cabazitaxel, capecitabine, carboplatin, cisplatin, cyclophosphamide, cytarabine, dacarbazine, daunorubicin, docetaxel, doxorubicin, etoposide, fluorouracil, gemcitabine, irinotecan, lomustine, methotrexate, mitomycin C, oxaliplatin, paclitaxel, pemetrexed, temozolomide, vincristine), tyrosine kinase targeted-therapeutics (e.g.
- aldesleukin, interferon alfa-2b, ipilimumab, lambrolizumab, nivolumab, prednisone, sipuleucel-T) and angiogenesis-targeted therapies e.g. aflibercept, bevacizumab
- additional therapeutic agents may be administered with one or more compounds of the invention as part of the same or separate dosage forms, via the same or different routes of administration, and on the same or different administration schedules according to standard pharmaceutical practice known to one skilled in the art.
- a pharmaceutical combination for treating cancer in a patient in need thereof which comprises (a) a compound of the invention or a pharmaceutically acceptable salt thereof, (b) an additional therapeutic agent and (c) optionally at least one pharmaceutically acceptable carrier for simultaneous, separate or sequential use for the treatment of a tumor disease, wherein the amounts of the compound or salt thereof and of the additional therapeutic agent are together effective in treating said cancer; (ii) a pharmaceutical composition comprising such a combination; (iii) the use of such a combination for the preparation of a medicament for the treatment of cancer; and (iv) a commercial package or product comprising such a combination as a combined preparation for simultaneous, separate or sequential use; and to a method of treatment of cancer a patient in need thereof.
- the combination therapy is for treating a cancer is selected from non-small cell lung cancer, papillary thyroid carcinoma, glioblastoma multiforme, acute myeloid leukemia, colorectal carcinoma, large cell neuroendocrine carcinoma, prostate cancer, neuroblastoma, pancreatic carcinoma, melanoma, head and neck squamous cell carcinoma and gastric carcinoma.
- Another embodiment of this invention provides a method of treating inflammation or an inflammatory disease or disorder in a mammal, comprising administering to said mammal in need thereof one or more compounds of Formula I or a pharmaceutically acceptable salt thereof in an amount effective to treat said inflammation.
- the inflammatory disease is inflammatory lung diseases (such as asthma), interstitial cystitis, bladder pain syndrome, inflammatory bowel diseases (including ulcerative colitis and Crohn's disease), and inflammatory skin diseases such as atopic dermatitis.
- the method of treating inflammation or an inflammatory disease or disorder comprises administering a compound of the invention in combination with one or more additional agents.
- additional agents include anti-TNF treatments (for example monoclonal antibody such as infliximab (Remicade), adalimumab (Humira), certolizumab pegol (Cimzia), and golimumab (Simponi), or a circulating receptor fusion protein such as etanercept (Enbrel)), antimetabolite and antifolate drug (for example Methotrexate), or targeted kinase inhibitors (for example JAK family inhibitors Ruxolitinib, Tofacitinib, CYT387, Lestaurtinib, Pacritinib and TGI 01348).
- anti-TNF treatments for example monoclonal antibody such as infliximab (Remicade), adalimumab (Humira), certolizumab pegol (Cimzia), and golimumab (Simponi
- a circulating receptor fusion protein such as etanercept (
- Another embodiment of this invention provides a method of treating Trypanosoma cruzi infection in a mammal, comprising administering to said mammal in need thereof one or more compounds of Formula I or a pharmaceutically acceptable salt thereof in an amount effective to treat said Trypanosoma cruzi infection.
- Another embodiment of this invention provides a method of treating Sjogren's syndrome in a mammal, comprising administering to said mammal in need thereof one or more compounds of Formula I or a pharmaceutically acceptable salt thereof in an amount effective to treat said syndrome.
- Another embodiment of this invention provides a method of treating endometriosis in a mammal, comprising administering to said mammal in need thereof one or more compounds of Formula I or a pharmaceutically acceptable salt thereof in an amount effective to treat said endometriosis.
- Another embodiment of this invention provides a method of treating diabetic peripheral neuropathy in a mammal, comprising administering to said mammal in need thereof one or more compounds of Formula I or a pharmaceutically acceptable salt thereof in an amount effective to treat said diabetic peripheral neuropathy.
- Another embodiment of this invention provides a method of treating prostatitis in a mammal, comprising administering to said mammal in need thereof one or more compounds of Formula I or a pharmaceutically acceptable salt thereof in an amount effective to treat said prostatitis.
- Another embodiment of this invention provides a method of treating pelvic pain syndrome in a mammal, comprising administering to said mammal in need thereof one or more compounds of Formula I or a pharmaceutically acceptable salt thereof in an amount effective to treat said pelvic pain syndrome.
- Another embodiment of this invention provides a method of treating a neurodegenerative disease in a mammal, comprising administering to said mammal in need thereof one or more compounds of Formula I or a pharmaceutically acceptable salt thereof in an amount effective to treat said neurodegenerative disease.
- Another embodiment of this invention provides a method of treating diseases related to an imbalance of the regulation of bone remodeling in a mammal, comprising administering to said mammal in need thereof one or more compounds of Formula I or a pharmaceutically acceptable salt thereof in an amount effective to treat said disease.
- the disease is osteoporosis, rheumatoid arthritis, and bone metastases.
- the method for treating diseases related to an imbalance of the regulation of bone remodeling in a mammal comprises administering a TrkA inhibitor of the invention in combination with one or more additional therapeutic agents or therapies.
- additional therapeutic agents or therapies include anti-TNF treatments (for example monoclonal antibody such as infliximab (Remicade), adalimumab (Humira), certolizumab pegol (Cimzia), and golimumab (Simponi), or with a circulating receptor fusion protein such as etanercept (Enbrel)), antimetabolite and antifolate drug (for example Methotrexate), or targeted kinase inhibitors (for example JAK family inhibitors Ruxolitinib, Tofacitinib, CYT387, Lestaurtinib, Pacritinib and TGI 01348).
- anti-TNF treatments for example monoclonal antibody such as infliximab (Remicade), adalim
- an "effective amount” means an amount of compound that, when administered to a mammal in need of such treatment, is sufficient to (i) treat a particular disease, condition, or disorder which can be treated with a compound of Formula I, or (ii) attenuate, ameliorate, or eliminate one or more symptoms of the particular disease, condition, or disorder described herein.
- the amount of a compound of Formula I that will correspond to such an amount will vary depending upon factors such as the particular compound, disease condition and its severity, the identity (e.g., weight) of the mammal in need of treatment, but can nevertheless be routinely determined by one skilled in the art.
- the term "mammal” refers to a warm-blooded animal that has or is at risk of developing a disease described herein and includes, but is not limited to, guinea pigs, dogs, cats, rats, mice, hamsters, and primates, including humans.
- the compounds of the present invention can be used in combination with one or more additional therapeutic agents that work by the same or a different mechanism of action.
- additional therapeutic agents include anti-inflammatory compounds, steroids (e.g., dexamethasone, cortisone and fluticasone), analgesics such as NSAIDs (e.g., aspirin, ibuprofen, indomethacin, and ketoprofen), and opioids (such as morphine), and chemotherapeutic agents.
- a pharmaceutical combination comprising an effective amount of: (a) at least one compound of Formula I; and (b) at least one additional therapeutic agent selected from anti-inflammatory compounds, steroids (e.g., dexamethasone, cortisone and fluticasone), analgesics such as NSAIDs (e.g., aspirin, ibuprofen, indomethacin, and ketoprofen), and opioids (such as morphine), for use in the treatment of pain in a mammal, wherein (a) and (b) can be in separate dosage forms or in the same dosage form.
- steroids e.g., dexamethasone, cortisone and fluticasone
- analgesics such as NSAIDs (e.g., aspirin, ibuprofen, indomethacin, and ketoprofen)
- opioids such as morphine
- the term "pharmaceutical combination” as used herein refers to a pharmaceutical therapy resulting from the mixing or combining of more than one active ingredient and includes both fixed and non-fixed combinations of the active ingredients.
- the term "fixed combination” means that at least one of the compounds of Formula I, and at least one additional therapeutic agent are both administered to a patient simultaneously in the form of a single entity or dosage.
- the term “non-fixed combination” means that at least one of the compounds of Formula I, and at least one additional therapeutic agent, are administered to a patient as separate entities either simultaneously or sequentially with variable intervening time limits, wherein such administration provides effective levels of the two or more compounds in the body of the patient.
- cocktail therapies e.g. the administration of three or more active ingredients.
- Also provided herein is a method of treating pain in a mammal, comprising co-administering to a mammal in need thereof an effective amount of: (a) at least one compound of Formula I; and (b) at least one additional therapeutic agent selected from antiinflammatory compounds, steroids (e.g., dexamethasone, cortisone and fluticasone), analgesics such as NSAIDs (e.g., aspirin, ibuprofen, indomethacin, and ketoprofen), opioids (such as morphine), calcitonin gene-related peptide receptor antagonists, subtype-selective ion channel modulators, anticonvulsants (for example Pregabalin and gabapentin), dual serotonin-norepinephrin reuptake inhibitors (for example duloxetine, venlafaxine and milnacipran), and tricyclic antidepressants (such as amitriptyline, nortrip
- co-administering is meant to encompass administration of the selected therapeutic agents to a single patient, and is intended to include treatment regimens in which the agents are administered by the same or different route of administration or at the same or different times.
- This term encompasses administration of two or more agents to a mammal so that both agents and/or their metabolites are present in the mammal at the same time. It includes simultaneous administration in separate compositions, administration at different times in separate compositions, and/or administration in a composition in which both agents are present.
- the compound(s) of the invention and the other therapeutic agent(s) are administered in a single composition.
- compound(s) of the invention and the other agent(s) are admixed in the composition.
- steroids e.g., dexamethasone, cortisone and fluticasone
- analgesics such as NSAIDs (e.g., aspirin, ibuprofen, indomethacin, and ketoprofen)
- opioids such as morphine
- steroids e.g., dexamethasone, cortisone and fluticasone
- analgesics such as NSAIDs (e.g., aspirin, ibuprofen, indomethacin, and ketoprofen)
- opioids such as morphine
- Compounds of the invention may be administered by any convenient route, e.g. into the gastrointestinal tract (e.g. rectally or orally), the nose, lungs, musculature or vasculature, or transdermally or dermally.
- Compounds may be administered in any convenient administrative form, e.g. tablets, powders, capsules, solutions, dispersions, suspensions, syrups, sprays, suppositories, gels, emulsions, patches etc.
- Such compositions may contain components conventional in pharmaceutical preparations, e.g. diluents, carriers, pH modifiers, sweeteners, bulking agents, and further active agents. If parenteral administration is desired, the compositions will be sterile and in a solution or suspension form suitable for injection or infusion. Such compositions form a further aspect of the invention.
- Another formulation may be prepared by mixing a compound described herein and a carrier or excipient.
- Suitable carriers and excipients are well known to those skilled in the art and are described in detail in, e.g., Ansel, Howard C, et al., Ansel's Pharmaceutical Dosage Forms and Drug Delivery Systems. Philadelphia: Lippincott, Williams & Wilkins, 2004; Gennaro, Alfonso R., et al. Remington: The Science and Practice of Pharmacy. Philadelphia: Lippincott, Williams & Wilkins, 2000; and Rowe, Raymond C. Handbook of Pharmaceutical Excipients. Chicago, Pharmaceutical Press, 2005.
- the formulations may also include one or more buffers, stabilizing agents, surfactants, wetting agents, lubricating agents, emulsifiers, suspending agents, preservatives, antioxidants, opaquing agents, glidants, processing aids, colorants, sweeteners, perfuming agents, flavoring agents, diluents and other known additives to provide an elegant presentation of the drug (i.e., a compound described herein or pharmaceutical composition thereof) or aid in the manufacturing of the pharmaceutical product (i.e., medicament).
- buffers stabilizing agents, surfactants, wetting agents, lubricating agents, emulsifiers, suspending agents, preservatives, antioxidants, opaquing agents, glidants, processing aids, colorants, sweeteners, perfuming agents, flavoring agents, diluents and other known additives to provide an elegant presentation of the drug (i.e., a compound described herein or pharmaceutical composition thereof) or aid in the manufacturing of the
- composition which comprises a compound of Formula I or a pharmaceutically acceptable salt thereof, as defined hereinabove, together with a pharmaceutically acceptable diluent or carrier.
- the present invention provides a compound of Formula I or a pharmaceutically acceptable salt thereof, for use in the treatment of pain in a mammal.
- the pain is chronic pain.
- the pain is acute pain.
- the pain is inflammatory pain, neuropathic pain, or pain associated with cancer, surgery, or bone fracture.
- the present invention provides a compound of Formula I or a pharmaceutically acceptable salt thereof, for use in the treatment of cancer in a mammal.
- the present invention provides a compound of Formula I or a pharmaceutically acceptable salt thereof, for use in the treatment of inflammation or an inflammatory disease or disorder in a mammal.
- the inflammatory disease is inflammatory lung diseases (such as asthma), interstitial cystitis, bladder pain syndrome, inflammatory bowel diseases (including ulcerative colitis and Crohn's disease), and inflammatory skin diseases such as atopic dermatitis.
- the present invention provides a compound of Formula I or a pharmaceutically acceptable salt thereof, for use in the treatment of infectious diseases, for example Trypanosoma cruzi infection, in a mammal.
- the present invention provides a compound of
- Formula I or a pharmaceutically acceptable salt thereof, for use in the treatment of Sjogren's syndrome in a mammal.
- the present invention provides a compound of Formula I or a pharmaceutically acceptable salt thereof, for use in the treatment of endometriosis in a mammal.
- the present invention provides a compound of Formula I or a pharmaceutically acceptable salt thereof, for use in the treatment of diabetic peripheral neuropathy in a mammal, [00485] In another embodiment, the present invention provides a compound of Formula I or a pharmaceutically acceptable salt thereof, for use in the treatment of prostatitis in a mammal,
- the present invention provides a compound of Formula I or a pharmaceutically acceptable salt thereof, for use in the treatment of pelvic pain syndrome in a mammal,
- the present invention provides a compound of Formula I or a pharmaceutically acceptable salt thereof, for use in the treatment of a neurodegenerative disease in a mammal.
- the present invention provides the use of a compound of Formula I or a pharmaceutically acceptable salt thereof, in the manufacture of a medicament for the treatment of a condition selected from pain, cancer, inflammation, neurodegenerative disease or Trypanosoma cruzi infection.
- the condition is chronic pain.
- the condition is acute pain.
- the pain is inflammatory pain, neuropathic pain, or pain associated with cancer, surgery, or bone fracture.
- the condition is cancer.
- the condition is inflammation.
- the condition is a neurodegenerative disease.
- the condition is Trypanosoma cruzi infection.
- the condition is Sjogren's syndrome.
- the condition is endometriosis.
- the condition is diabetic peripheral neuropathy.
- the condition is prostatitis.
- the condition is pelvic pain syndrome.
- TrkA binding activity was determined in a TrkA LanthaScreenTM Eu Kinase Binding Assay. 5 nM His-tagged recombinant human TrkA (6HIS tagged cytoplasmic domain from Invitrogen, Catalog No. PV3144) was incubated with 4 nM Alexa-Fluor® Tracer 236 (Invitrogen Cat. No.PV5592), 2 nM biotinylated anti-His (Invitrogen Cat. No. PV6090), and 2 nM europium-labeled Streptavidin (Invitrogen Cat. No.
- Table A provides averaged IC 50 values for compounds of the invention when tested in the assay of Example A, where A represents an averaged IC 50 value ⁇ 100 nM.
- p38a binding activity was determined in a p38a LanthaScreenTM Eu Kinase Binding Assay. 5nM of inactive, GST-tagged recombinant human p38a (GST-tagged cytoplasmic domain from Invitrogen, Catalog No. PV3305) was incubated with 5nM Alexa- Fluor® Tracer 199 (Invitrogen Cat. No.PV5830), and 2nM europium labeled anti-GST antibody (Invitrogen Cat. No. PV5594), in buffer (25mM [Na + ] HEPES pH 7.3, lOmM MgCl 2 , ⁇ NaV0 4 ).
- Step A Preparation of 2-methoxy-N-((trimethylsilyl)methyl)ethanamine: To a DMSO solution (15 mL) of 2-methoxyethanamine (14.2 mL, 163 mmol) at 90 °C was added a DMSO (10 mL) solution of (chloromethyl)trimethylsilane (1 1.4 mL, 81.5 mmol) by addition funnel over 40 minutes. The mixture was heated at 90 °C for 3.5 hours then cooled to ambient temperature. The mixture was then diluted with H 2 0 (150 mL) and extracted with EtOAc (2 x 150 mL).
- Step B Preparation of 2-methoxy-N-(methoxymethyl)-jV-
- Step A Preparation of (E)-l-fluoro-4-(2-nitrovinyl)benzene: Acetic acid (2.0 L, 35.5 mol) and ammonium acetate (310.5 g, 4.03 mol) were stirred at ambient temperature for 1 hour, then nitromethane (611 mL, 11.3 mol) and 4-fluorobenzaldehyde (200 g, 1.61 mol) were added and the reaction mixture was heated to 90 °C for 3 hours. The reaction was allowed to cool to ambient temperature, then H 2 0 (4 L) was added over 2 hours with mechanical stirring. The suspension was stirred 1 hour, then filtered and washed with 2:1 water/acetic acid (500 mL).
- Step B Preparation of tr »5 , -3-(4-fluorophenyl)- 1 -(2-methoxyethyl)-4-nitro- pyrrolidine: To a suspension of (E)-l-fluoro-4-(2-nitrovinyl)benzene (201 g, 1.20 mol) in DCM (1.09 L) and TFA (9.3 mL, 120 mmol) was added dropwise over 30 minutes 2- methoxy-N-(methoxymethyl)-N-((trimethylsilyl)methyl)ethanamine (Preparation A; 383 g, 1.86 mol) and the internal reaction temperature was maintained between 23-36 °C by cooling in an ice bath.
- Step C Preparation of trafts-4-(4-fluorophenyl)-l-(2- methoxyethyl)pyrrolidin-3-amine: To a solution of tra « 1 y-3-(4-fluorophenyl)-l-(2- methoxyethyl)-4-nitropyrrolidine (289 g, 1.08 mol) in EtOH (1 L) was added platinum(IV) oxide (24.5 g, 108 mmol) in a Parr vessel and installed into a Parr shaker. The vessel was evacuated and backfilled with nitrogen (3x), then evacuated and backfilled with hydrogen (60 psi). The vessel was recharged with hydrogen as needed until the reaction was complete.
- Step D Preparation of (3S,4R)-4-(4-fluorophenyl -l-(2- methoxyethyl)pyrrolidin-3 -amine (2S,3S -2,3-bis(4-methylbenzoyloxy)succinate: To a solution of (3S,4R)-4-(4-fluorophenyl)-l-(2-methoxyethyl)pyrrolidin-3-amine (120 g, 504 mmol) in THF (3.0 L) and H 2 0 (333 mL) was added di-/?-toluoyl-D-tartaric acid (195 g, 504 mmol).
- Step E Preparation of (3£4i?)-4-(4-fluorophenyl)-l-(2- methoxyethyl)pyrrolidin-3-amine: (3 S,4R)-4-(4-fluorophenyl)- 1 -(2-methoxyethyl)pyrrolidin- 3-amine (2S,3S)-2,3-bis(4-methylbenzoyloxy)succinate (20 g, 32.0 mmol) was dissolved in DCM (300 mL) and washed with 1M NaOH (2 x 200 mL). The combined aqueous phases were extracted with DCM (200 mL).
- Step A Preparation of (E)-3-(3,4,5-trifluorophenyl)acryloyl chloride: To a suspension of (E)-3-(3,4,5-trifluorophenyl)acrylic acid (5.15 g, 25.5 mmol) in toluene (50 mL) was added oxalyl chloride (4.43 mL, 51.0 mmol) and the mixture was stirred for 5 minutes at ambient temperature. The mixture was cooled to 0 °C and DMF (0.0493 mL, 0.637 mmol) was added (immediate, mild gas evolution). The mixture was stirred for 10 minutes, the ice bath was removed and the mixture allowed to reach ambient temperature (sustained gas evolution).
- Step B Preparation of ( ?.E)-4-phenyl-3-(3-(3A5- trifluorophenyl)acryloyl)oxazolidin-2-one: A solution of (/?)-4-phenyloxazolidin-2-one (3.92 g, 24.0 mmol) in THF (60 mL) was cooled to -78 °C and lithium bis(trimethylsilyl)amide (25.2 mL, 25.2 mmol, 1.0 M in THF) was added dropwise over 10 minutes.
- Step C Preparation of (i? -3-r(3S.4i?Vl-( ' 2-methoxyethvn-4- .4.5- trifluorophenyl)pyrrolidine-3-carbonyl)-4-phenyloxazolidin-2-one: A solution of (R,E)-4- phenyl-3-(3-(3,4,5-trifluorophenyl)acryloyl)oxazolidin-2-one (9.50 g, 27.4 mmol) and TFA (2.11 mL, 2.74 mmol) in toluene (270 mL) was cooled to 0 °C and 2-methoxy-N- (methoxymethyl)-N-((trimethylsilyl)methyl)ethanamine (Preparation A, 8.43 g, 41.0 mmol) in toluene (25 mL) was added dropwise over 15 minutes.
- Step D Preparation of f3SAK)-l-(2-methoxyethvn-4-(3A5- trifluorophenyl)pyrrolidine-3-carboxylic acid: A 1M aqueous solution of LiOH (39.0 mL, 39.0 mmol) was cooled to 0 °C and H 2 0 2 (3.37 mL, 33.0 mmol, 30 wt%) was added.
- Step E Preparation of benzyl C3S.4i?>l-(2-methoxyethyl)-4-(3.4.5- trifluorophenyl)pyrrolidin-3-ylcarbamate: To a solution of (3S',4 ?)-l-(2-methoxyethyl)-4- (3,4,5-trifluorophenyl)pyrrolidine-3-carboxylic acid (4.0 g, 1 1.9 mmol) in toluene (50 mL) was added DIEA (5.18 mL, 29.7 mmol) followed by diphenyl phosphoryl azide (5.3 mL, 27.3 mmol).
- Step F Preparation of (3S.4i?)-l-(2-methoxyethyr)-4-(3A5- trifluorophenyl)pyrrolidin-3 -amine dihvdrochloride: A mixture of benzyl (35,4/?)- 1 -(2- methoxyethyl)-4-(3,4,5-trifluorophenyl)pyrrolidin-3-ylcarbamate (1.05 g, 2.31 mmol) and TFA (15 mL) was heated at 60 °C for 7 hours. Additional TFA (10 mL) was added and the mixture heated at 75 °C for 1 hour. The reaction mixture was cooled to ambient temperature and concentrated in vacuo.
- Step A Preparation of tert-butyl (3SAR)-4-(3 -fluorophenyl)- 1 -(2- methoxyethvDp yrrolidin-3 -ylcarbamate : A solution of tert-butyl (35,4i?)-4-(3- fluorophenyl)pyrrolidin-3-ylcarbarnate (250 mg, 0.89 mmol, commercially available), DIEA (0.48 mL, 2.68 mmol) and l-bromo-2-methoxyethane (149 mg, 1.07 mmol) in DMF (3 mL) was stirred at ambient temperature for 2 hours, then heated to 60 °C for 4 hours, then cooled to ambient temperature overnight.
- Step A Preparation of tra ⁇ -l-benzyl-3-nitro-4-phenylpyrrolidine: To a
- Step B Preparation of trq3 ⁇ 4s-l-benzyl-4-phenylpyrrolidin-3 -amine: To a suspension of tra «5-l-benzyl-3-nitro-4-phenyl -pyrrolidine (93.9 g, 333 mmol) in EtOH (1.20 L) was added concentrated HC1 (450 mL), followed by addition of zinc dust (173 g, 2.66 mol) in small portions over 1.5 hours while maintaining the temperature between 55-60 °C. The reaction mixture was stirred at ambient temperature for 18 hours, then cooled in an ice/water bath followed by addition of concentrated NH 4 OH (900 mL).
- Step C Preparation of trfl/3 ⁇ 45-(l-benzyl-4-phenyl-pyrrolidin-3-yl)-carbamic acid tert-butyl ester: To a mixture of tr ra- l-benzyl-4-phenylpyrrolidin-3 -amine (85.0 g, 333 mmol), THF (750 mL) and triethylamine (69.6 mL, 500 mmol), was slowly added (Boc) 2 0 (72.7 g, 333 mmol) in portions over 30 minutes. The reaction mixture was stirred at ambient temperature for 16 hours and was concentrated in vacuo.
- Step A Preparation of /ra ⁇ -N-(l-benzyl-4-phenylpyrrolidin-3-yl)-2,2,2- trifluoroacetamide : To a solution of trans-l -benzyl -4-phenylpyrrolidin-3 -amine (Preparation A- 100, Step B, 61.9 g, 245 mmol) in DCM (400 mL) was added DIEA (64.1 mL, 368 mmol) and the mixture was cooled in an ice bath. Trifluoroacetic anhydride (38.1 mL, 270 mmol) was added dropwise over 30 minutes under a N 2 atmosphere.
- Step B Preparation of trans-tert-butv ⁇ -3 -phenyl-4-(2,2,2-trifluoroacetamido) pyrrolidine- 1 -carboxylate: A solution of tra «s-N-(l-benzyl-4-phenylpyrrolidin-3-yl)-2,2,2- trifluoroacetamide (78.7 g, 226 mmol) in EtOH (400 mL) was purged with N 2 and treated with 20% Pd(OH) 2 on activated carbon (31.7 g, 45.2 mmol).
- Step C Preparation of trans-tert-butyl 3-amino-4-phenylpyrrolidine-l- carboxylate: A solution of trans tert-butyl 3-phenyl-4-(2,2,2-trifluoroacetamido)pyrrolidine- 1-carboxylate (63.2 g, 176 mmol) in MeOH (200 mL) was cooled in an ice bath and 2 N NaOH (220 mL, 440 mmol) was added. The reaction mixture was allowed to warm to ambient temperature overnight, then concentrated to approximately 200 mL and diluted with H 2 0 (200 mL).
- Step A Preparation of tert-butyl tr w5 , -l-(2-methoxyethyl)-4- phenylpyrrolidin-3-ylcarbamate.
- tert-butyl tr£ms-4-phenylpyrrolidin-3- ylcarbamate Preparation A-100, 4.82 g, 17.5 mmol
- dry DMF 50 mL
- DIEA 9.12 mL, 52.4 mmol
- 1 -bromo-2-methoxyethane (1.97 mL, 20.9 mmol).
- Step B Preparation of trans- 1 -(2-methoxyethyl)-4-phenylpyrrolidin-3 -amine dihydrochloride: To a solution of tert-butyl tra «5 , -l-(2-methoxyethyl)-4-phenylpyirolidin-3- ylcarbamate (5.10 g, 15.9 mmol) in 2:1 EtOAc-MeOH (150 mL) was added 4 N HCl in dioxane (59.7 mL, 239 mmol). The mixture was stirred at ambient temperature for 90 minutes and then concentrated in vacuo.
- Step A Preparation of (i?)-3-cinnamoyl-4-phenyloxazolidin-2-one: A THF (50 mL) solution of (i?)-4-phenyloxazolidin-2-one (5.90 g, 36.2 mmol) was cooled to -78 °C and treated with lithium bis(trimethylsilyl)amide (36.9 mL, 36.9 mmol, 1.0 M in THF) dropwise over 15 minutes. After 15-minute stirring at -78 °C, a THF (10 mL) solution of cinnamoyl chloride (6.33 g, 38.0 mmol) was then introduced.
- Step B Preparation of (i?V3-((35'.4i?)-l-(2-methoxyethvn-4- phenylpyrrolidine-3-carbonyl)-4-phenyloxazolidin-2-one: A toluene (500 mL) solution of (R)-3-cinnamoyl-4-phenyloxazolidin-2-one (8.00 g, 27.3 mmol) and TFA (0.210 mL, 2.73 mmol) was first cooled to 5-10 °C, followed by dropwise addition of a toluene (30 mL) solution of 2-methoxy-N-(methoxymethyl)-N-((trimethylsilyl)methyl)ethanamine (Preparation C, 8.40 g, 40.9 mmol).
- Step C Preparation of (3S.4 ⁇ )-l-(2-methoxyethyl)-4-phenylpyrrolidine-3- carboxylic acid: To a 1M aqueous solution of LiOH (41.2 mL, 41.2 mmol) at 0 °C was added H 2 0 2 (3.37 mL, 33.0 mmol, 30 wt%).
- Step D Preparation of benzyl (3SAR)- 1 -(2-methoxyethyl)-4-phenylpyrrolidin- 3 -ylcarbamate: To a solution of (3S,4i?)-l-(2-methoxyethyl)-4-phenylpyrrolidine-3- carboxylic acid (4.11 g, 16.5 mmol) in toluene (70 mL) was added TEA (5.74 mL, 41.2 mmol) followed by diphenyl phosphoryl azide (4.99 mL, 23.1 mmol). The mixture was stirred at ambient temperature for 1 hour and then heated to reflux for 1 hour.
- Step E Preparation of (35'.4i?)-l-(2-methoxyethyl)-4-phenylpyrrolidin-3- amine dihvdrochloride: Benzyl (3S,4i?)-l-(2-methoxyethyl)-4-phenylpyrrolidin-3- ylcarbamate (0.257 g, 0.725 mmol) and TFA (3.91 mL, 50.8 mmol) were heated at 60 °C for 17 hours.
- Step A Preparation of (/?.E)-3-(3-(3,5-difluorophenyl)acryloyl)-4- phenyloxazolidin-2-one : To a solution of (E)-3-(3,5-difluorophenyl)acrylic acid (10.0 g, 54.3 mmol) in Et 2 0 (150 mL) at 0 °C was added DIEA (9.48 mL, 54.3 mmol) followed by pivaloyl chloride (6.69 mL, 54.3 mmol). The mixture was stirred at 0 °C for 1 hour and cooled to - 78 °C.
- the reaction mixture was quenched with saturated NH 4 C1 (25 mL), diluted with EtOAc (600 mL), washed with water, NaHC0 3 , and brine, dried over MgS0 4 , and concentrated in vacuo.
- the crude material was purified by silica column chromatography, eluting with 10-20% Ethyl acetate/Hexanes to afford the product ( 11.0 g, 61.5% yield).
- Step A Preparation of tert-butyl (3£4j?Vl-(2-methoxyethyl>4-(3- (trifluoromethyl)-phenyl)pyrrolidin-3 -ylcarbamate : A solution of tert-butyl (3S,4i?)-4-(3- (trifluoromethyl)phenyl)-pyrrolidin-3-ylcarbamate (100 mg, 0.303 mmol, commercially available), N,N-diethylpropan-2-amine (0.145 mL, 0.908 mmol) and l-bromo-2- methoxyethane (0.0361 mL, 0.363 mmol) in DMF (1 mL) was stirred at ambient temperature for 2 hours, then heated to 60 °C for 4 hours, then cooled to ambient temperature overnight.
- Step A (E)-2-fluoro-5-(2-nitrovinyl)benzonitrile.
- 2-fluoro-5- formylbenzonitrile (3.84 g, 25.0 mmol) in 3: 1 CH 3 N0 2 /CH 3 CN (25 mL) was added DMAP (0.305 g, 2.50 mmol) and the mixture stirred at ambient temperature for 23 hours.
- the mixture was cooled on an ice bath and Ac 2 0 (3.54 mL, 37.5 mmol) was added. The mixture was stirred for 5 minutes, allowed to reach ambient temperature and stirred for 1 hour. The mixture was concentrated to a yellow solid.
- Step B: 7>a» -2-fluoro-5-(l-(2-methoxyethyl)-4-nitropyrrolidin-3- yPbenzonitrile: Using (E)-2-fluoro-5-(2-nitrovinyl)benzonitrile in Step B of the procedure describe in Preparation Bl, the title compound was prepared as light gold syrup (1.56 g, 53%). MS (apci) m/z 294.1 (M+H).
- Step C rfl « -5-(4-amino-l-(2-methoxyethyl)pyrrolidin-3-yl)-2- fluorobenzonitrile:
- a solution of tran5 , -2-fluoro-5-(l-(2-methoxyethyl)-4-nitropyrrolidin-3- yl)benzonitrile (450 mg, 1.53 mmol) in MeOH (6.0 mL) was cooled to 0 °.
- Zn dust (1.00 mg, 15.3 mmol) and saturated aqueous NH 4 C1 (1.0 mL) were added sequentially and the mixture was stirred for 5 minutes. The mixture was allowed to reach ambient temperature and stirred until complete by LCMS analysis.
- Step B rfl « , -3-(4-amino-l-(2-methoxyethyl)pyrrolidin-3-yl)-5- fluorobenzonitrile :
- the tile compound was prepared using 3-fluoro-5-formylbenzonitrile in the procedure described for the preparation of tra «5-5-(4-amino-l-(2- methoxyethyl)pyrrolidin-3-yl)-2-fluorobenzonitrile (Preparation N-100).
- the compound was isolated as a colorless syrup (542 mg, 93%).
- MS (apci) m/z 264.1 (M+H).
- Step A rra»5 , -3-(4-chlorophenyl)-l-(2-methoxyethyl)-4-nitropyrrolidine:
- Step B rra».y-l-(2-methoxyethyl)-4-(4-chlorophenyl)pyrrolidin-3-amine: To a suspension of 2800 Raney Nickel (50 wt% in H 2 0, 0.873 g, 5.10 mmol) in MeOH (25 mL) was added tran5 , -3-(4-chlorophenyl)-l-(2-methoxyethyl)-4-nitropyrrolidine (2.90 g, 10.2 mmol) in MeOH (25 mL). The mixture was flushed with H 2 gas and stirred under a balloon atmosphere of H for 16 hours.
- Step A Preparation of 5-amino-4-methyl-l -phenyl- 1 H-pyrazol-3 (2H)-one: A mixture of ethyl 2-cyanopropanoate (50.5 g, 397.2 mmol) and phenylhydrazine (39 mL, 397.2 mmol) in dioxane (100 mL) was heated at 1 10 °C for 5 days. The cooled mixture was concentrated to 1/2 volume then cooled in ice and triturated with cold Et 2 0.
- Step B Preparation of 5-amino-4-methyl-l-phenyl-lH-pyrazol-3-yl trifluoromethane sulfonate: A suspension of 5-amino-4-methyl-l -phenyl- lH-pyrazol-3(2H)- one (13.72 g, 72.5 mmol) and N-phenylbis(trifluoromethylsulfonamide) (27.2 g, 76.1 mmol) in DMF (100 mL) was treated with DIEA (37.9 mL, 217.5 mmol) and the mixture stirred at ambient temperature for 16 hours.
- DIEA 37.9 mL, 217.5 mmol
- Step A Preparation of 4-methyl-3-(6-methylpyridin-3-yl)-l-phenyl-lH- pyrazol-5 -amine: 5-Amino-4-methyl-l-phenyl-lH-pyrazol-3-yl trifluoromethane sulfonate
- Preparation E (1.01 g, 3.11 mmol), (6-methylpyridin-3-yl)boronic acid (639 mg, 4.67 mmol), K 2 C0 3 (1.72 g, 12.45 mmol) and Pd(PPh 3 ) 4 (360 mg, 0.31 mmol) were combined in toluene (10 mL), water (5 mL) and EtOH (2.5 mL) and stirred at 95 °C in a sealed tube for 18 hours.
- Step B Preparation of l-((3S,4R)-4-(3.4-difluorophenyl)-l-(2- methoxyethyl)pyrrolidin-3-yl)-3-(4-methyl-3-(6-methylpyridin-3-yl)-l-phenyl-lH-pyrazol-5 vDurea: To a solution of 4-methyl-3-(6-methylpyridin-3-yl)-l -phenyl- lH-pyrazol-5 -amine (40 mg, 0.15 mmol) in DCM (2 mL) was added triphosgene (22 mg, 0.07 mmol) followed by DIEA (79 ⁇ , 0.46 mmol).
- Step A Preparation of phenyl (3 -bromo-4-methyl-l -phenyl- lH-pyrazol-5- vDcarbamate: To a solution of 3-bromo-4-methyl-l-phenyl-lH-pyrazol-5-amine [Preparation F] (339 mg, 1.34 mmol) in EtOAc (10 mL) was added 2N NaOH (2 mL, 4.0 mmol) followed by phenyl chloroformate (337 ⁇ ⁇ , 2.69 mmol).
- Step B Preparation of l-(3-bromo-4-methyl-l-phenyl-lH-pyrazol-5-yl)-3- ((3 S,4RV4-(3 ,4-difluorophenyl)- 1 -(2-methoxyethyl)pyrrolidin-3 -yl)urea: To a solution of (35,4 ⁇ )-4-(3,4-difluorophenyl)-l-(2-methoxyethyl)pyrrolidin-3-amine [Preparation B3] (464 mg, 1.41 mmol) and phenyl (3-bromo-4-methyl-l -phenyl- lH-pyrazol-5-yl)carbamate (500 mg, 1.34 mmol) in DCM (10 mL) was added DIEA (819 ⁇ , 4.7 mmol).
- Step C 1 -(3 -(2-(cyclopropylamino)pyrimidin-5 -yl)-4-methyl- 1 -phenyl- 1 H- pyrazol-5-yl)-3-((3S,4R)-4-(3,4-difluorophenyl)-l-(2-methoxyethyl pyrrolidin-3-yl)urea: 1- (3-Bromo-4-methyl- 1 -phenyl- 1 H-pyrazol-5-yl)-3-((3S,4i?)-4-(3,4-difluorophenyl)- 1 -(2- methoxyethyl) pyrrolidin-3-yl)urea (100 mg, 0.19 mmol), N-cyclopropyl-5-(4,4,5,5- tetramethyl-l,3,2-dioxaborolan-2-yl)pyrimidin-2-amine (147 mg, 0.56 mmol) and tricyclohe
- Step A Preparation of 5-(5-amino-4-methyl-l -phenyl- lH-pyrazol-3- yl)pyrimidin-2( 1 H -one hydrochloride: A solution of 3-(2-methoxypyrimidin-5-yl)-4- methyl- 1 -phenyl- lH-pyrazol-5-amine [Prepared as in 1, Step A] (200 mg, 0.71 mmol) in methanol (5 mL) was treated with 5-6 N HCl/isopropyl alcohol (5 mL) and stirred at reflux for 4 hours.
- Step B Preparation of 5-(5-amino-4-methvI-l -phenyl-lH-pyrazol-3-yl)-l- methylpyrimidin-2( 1 H)-one: A solution of 3-(2-methoxypyrimidin-5-yl)-4-methyl-l-phenyl- lH-pyrazol-5-amine (50 mg, 0.16 mmol) DMA (1 mL) was treated with Cs 2 C0 3 (161 mg, 0.49 mmol) and stirred at ambient temperature for 30 minutes. Methyl iodide (20 ⁇ , 0.33 mmol) was then added and the mixture stirred, capped, at ambient temperature for 16 hours.
- Step C Preparation of l-((3S,4R -4-(3,4-difluorophenyl)-l-(2- methoxyethyl)pyrrolidin-3-yl)-3-(4-methyl-3-( 1 -methyl-2-oxo- 1 ,2-dihvdropyrimidin-5-yl)- 1 - phenyl- 1 H-pyrazol-5-yl)urea: To a solution of 5-(5-amino-4-methyl-l-phenyl-lH-pyrazol-3- yl)-l-methylpyrimidin-2(lH)-one (23 mg, 0.08 mmol) in DCM (1 mL) was added tnphosgene (12 mg, 0.04 mmol) and the mixture treated with DIEA (43 ⁇ , 0.24 mmol).
- Step A Preparation of l ,3-dimethyl-5-(4.4,5.5-tetramethyl-l,3,2- dioxaborolan-2-yl)pyridin-2( 1 H)-one: 5-Bromo-l ,3-dimethylpyridin-l(l H)-one (1.0 g, 4.94 mmol), bis(pinnacolato)diboron (1.38 g, 5.44 mmol) and potassium acetate (1.46 g, 14.8 mmol) were combined in dioxane (10 mL) in a sealed vessel and the mixture was de-gassed with argon for 5 minutes.
- Step B Preparation of 5-(5-amino-4-methyl- 1 -phenyl- lH-pyrazol-3-yl)- 1.3- dimethylpyridin-2( 1 H)-one : 5-Amino-4-methyl-l-phenyl-lH-pyrazol-3-yl trifluoromethane sulfonate
- Preparation E (516 mg, 1.6 mmol), l ,3-dimethyl-5-(4,4,5,5-tetramethyl-l ,3,2- dioxaborolan-2-yl)pyridin-2(lH)-one (600 mg, 2.41 mmol), K 2 C0 3 (888 mg, 6.42 mmol) and Pd(PPh 3 ) 4 (185 mg, 0.16 mmol) were combined in toluene (10 mL), water (5 mL) and EtOH (2.5 mL) and warmed to 95 °C in a sealed vessel for 16 hours.
- Step C Preparation of l-((3S.4RV4-(3.4-difluorophenyl>l-(2-
- Step A Preparation of 4-methyl-3-(methylsulfonyl)-l -phenyl-lH-pyrazol-5- amine: 3-Bromo-4-methyl-l -phenyl- lH-pyrazol-5-amine [Preparation F] (300 mg, 1.19 mmol), sodium methanesulfinate (486 mg, 4.76 mmol) and copper iodide (249 mg, 1.31 mmol) were combined in DMSO (5 mL) and purged with bubbling argon for 5 minutes.
- Step B Preparation of phenyl i4-methyl-3-(methylsulfonyl>l-phenyl-lH- pyrazol-5-yl)carbamate: To a solution of 4-methyl-3-(methylsulfonyl)-l -phenyl- lH-pyrazol- 5-amine (45 mg, 0.18 mmol) in EtOAc (2 mL) was added 2N NaOH (269 ⁇ , 0.54 mmol) followed by phenyl chloroformate (45 ⁇ ,, 0.36 mmol). The mixture was stirred at ambient temperature for 16 hours, and then phenyl chloroformate (75 ⁇ ) was added and the mixture stirred for 4 hours.
- Step C Preparation of l-((3S,4R -4-(3.4-difluorophenyl -l-(2- methoxyethyl)pyrrolidin-3-yl)-3-(4-methyl-3-(methylsulfonyl)-l-phenyl-lH-pyrazol-5- yPurea: To a solution of (3S,4R)-4-(3,4-difluorophenyl)-l-(2-methoxyethyl)pyrrolidin-3- amine [Preparation B3] (38 mg, 0.15 mmol) in anhydrous DCM (2 mL) was added phenyl (4- methyl-3-(methylsulfonyl)-l -phenyl- lH-pyrazol-5-yl)carbamate (50 mg, 0.13 mmol) followed by DIEA (70 0.40 mmol).
- Step A Preparation of ethyl 3-cyano-2-oxobutanoate: To a solution of lithium bis(trimethylsilyl)amide (1.0 M in THF) (73.63 mL, 73.63 mmol) and THF (75 mL) under N 2 at -78 °C was added propionitrile (6.304 mL, 88.35 mmol) dropwise over 2 minutes, and the mixture was stirred for 1 hour. The mixture was then treated with diethyl oxalate (10 mL, 73.63 mmol) dropwise over 5 minutes, stirred at -78 °C for 45 minutes, and then stirred at 0 °C for 1 hour.
- propionitrile 6.304 mL, 88.35 mmol
- Step B Preparation of ethyl 5 -amino-4-methyl-l -phenyl- lH-pyrazole-3 - carboxylate: To a solution of ethyl 3-cyano-2-oxobutanoate (11.42 g, 73.6 mmol) in EtOH (300 mL) was added phenylhydrazine (7.2 mL, 73.6 mmol) followed by hydrogen chloride (5-6 M in iPrOH) (14.7 mL, 73.6 mmol). The reaction mixture was stirred at reflux for 16 hours, then cooled and concentrated to 50 mL.
- Step C Preparation of 5-amino-4-methyl-l-phenyl-lH-pyrazole-3-carboxylic acid: To a solution of ethyl 5-amino-4-methyl-l -phenyl- lH-pyrazole-3 -carboxylate (3.0 g, 12.2 mmol) in THF (24 mL) and MeOH (12 mL) was added LiOH (2M aq) (13.5 mL, 27.0 mmol) and the mixture was stirred at ambient temperature for 3 hours. The mixture was partially concentrated and then adjusted to pH 3 with 6M HC1 (4.5 mL) and extracted with 10% MeOH/DCM (3 x 25 mL).
- the aqueous phase was further acidified with 6M HC1 (1 mL) to pH 1, and then extracted with 10% MeOH/DCM (3 x 25 mL).
- the aqueous phase was saturated with NaCl and extracted with 10% MeOH/DCM (3 x 25 mL).
- the combined organic extracts were washed with brine (50 mL), dried over MgS0 4 , filtered and concentrated to afford 5-amino-4-methyl-l-phenyl-lH-pyrazole-3-carboxylic acid (2.4 g, 90% yield) as a tan solid.
- MS (apci) m/z 218.1 (M+H).
- Step D Preparation of 5-amino-N-methoxy-N,4-dimethyl-l -phenyl- 1H- pyrazole-3 -carboxamide : To a solution of 5-amino-4-methyl-l-phenyl-lH-pyrazole-3- carboxylic acid (1.0 g, 4.6 mmol) in ACN (46 mL) were added N,0-dimethylhydroxylamine hydrochloride (539 mg, 5.5 mmol) and DIEA (2.4 mL, 13.8 mmol). The mixture was stirred until a solution formed and was then treated with HATU (2.1 g, 5.52 mmol) and stirred at ambient temperature for 90 minutes.
- N,0-dimethylhydroxylamine hydrochloride 539 mg, 5.5 mmol
- DIEA 2.4 mL, 13.8 mmol
- Step E Preparation of l-(5-amino-4-methyl-l-phenyl-lH-pyrazol-3- yPethanone: A solution of 5 -amino-N-methoxy-N,4-dimethyl-l -phenyl- lH-pyrazole-3- carboxamide (365 mg, 1.40 mmol) in DCM (15 mL) was cooled to 0 °C under N 2 , and added MeMgBr (3M in Et 2 0) (491 ⁇ iL, 1.47 mmol) was added dropwise, over 4 minutes. The mixture was stirred at ambient temperature for 1 hour and then treated with DCM (5 mL) and stirred for 90 minutes.
- DCM 5 mL
- Step F Preparation of phenyl (3-acetyl-4-methyl-l -phenyl- lH-pyrazol-5- yPcarbamate: To a solution of l-(5-amino-4-methyl-l-phenyl-lH-pyrazol-3-yl)ethanone (89 mg, 0.41 mmol) in EtOAc (4 mL) were added NaOH (0.41 mL, 2M, 0.83 mmol) then phenylchloroformate (62 ⁇ , 0.49 mmol). The mixture was stirred at ambient temperature for 17 hours and then diluted with 10 mL EtOAc.
- Step G Preparation of l-(3-acetyl-4-methyl-l-phenyl-lH-pyrazol-5-vn-3- ((3S,4R -4-(3,4-difluorophenyl)-l-(2-methoxyethyl)pyrrolidin-3-yl)urea: A solution of (3S,4R)-4-(3,4-difluorophenyl)-l-(2-methoxyethyl)pyrrolidin-3-amine [Preparation B3] (105.8 mg, 0.41 mmol) in z ' PrOH (2 mL) was added to phenyl (3-acetyl-4-methyl-l -phenyl- lH-pyrazol-5-yl)carbamate (133 mg, 0.40 mmol).
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Application Number | Priority Date | Filing Date | Title |
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LTEP13795946.6T LT2922844T (en) | 2012-11-13 | 2013-11-12 | N-pyrrolidinyl, n`-pyrazolyl- urea, thiourea, guanidine and cyanoguanidine compounds as trka kinase inhibitors |
EP13795946.6A EP2922844B1 (en) | 2012-11-13 | 2013-11-12 | N-pyrrolidinyl, n'-pyrazolyl- urea, thiourea, guanidine and cyanoguanidine compounds as trka kinase inhibitors |
DK13795946.6T DK2922844T3 (en) | 2012-11-13 | 2013-11-12 | N-PYRROLIDINYL, N'-PYRAZOLYL-URINE, THIOURINE, GUANIDINE AND CYANOGUANIDE COMPOUNDS AS TRKA-KINASE INHIBITORS |
RS20180298A RS57001B1 (en) | 2012-11-13 | 2013-11-12 | N-pyrrolidinyl, n'-pyrazolyl- urea, thiourea, guanidine and cyanoguanidine compounds as trka kinase inhibitors |
NZ708028A NZ708028A (en) | 2012-11-13 | 2013-11-12 | N-pyrrolidinyl, n’-pyrazolyl- urea, thiourea, guanidine and cyanoguanidine compounds as trka kinase inhibitors |
ES13795946.6T ES2664331T3 (en) | 2012-11-13 | 2013-11-12 | Compounds of N-pyrrolidinyl, N'-pyrazolylurea, thiourea, guanidine and cyanoguanidine as Trka kinase inhibitors |
MX2015006046A MX365733B (en) | 2012-11-13 | 2013-11-12 | N-pyrrolidinyl, n'-pyrazolyl- urea, thiourea, guanidine and cyanoguanidine compounds as trka kinase inhibitors. |
RU2015122414A RU2677667C2 (en) | 2012-11-13 | 2013-11-12 | N-pyrrolidinyl-urea, n'-pyrazolyl-urea, thiourea, guanidine and cyanoguanidine compounds as trka kinase inhibitors |
UAA201505770A UA116455C2 (en) | 2012-11-13 | 2013-11-12 | N-pyrrolidinyl, n'-pyrazolyl- urea, thiourea, guanidine and cyanoguanidine compounds as trka kinase inhibitors |
CN201380058511.2A CN104781255B (en) | 2012-11-13 | 2013-11-12 | It is used as the N pyrrolidinyls of TRKA kinase inhibitors, N ' pyrazolyls urea, thiocarbamide, guanidine and cyanoguandine compounds |
AU2013344943A AU2013344943B2 (en) | 2012-11-13 | 2013-11-12 | N-pyrrolidinyl, n'-pyrazolyl- urea, thiourea, guanidine and cyanoguanidine compounds as TrkA kinase inhibitors |
KR1020157015411A KR102181915B1 (en) | 2012-11-13 | 2013-11-12 | N-pyrrolidinyl, n'-pyrazolyl-urea, thiourea, guanidine and cyanoguanidine compounds as trka kinase inhibitors |
CA2890876A CA2890876C (en) | 2012-11-13 | 2013-11-12 | N-pyrrolidinyl, n'-pyrazolyl- urea, thiourea, guanidine and cyanoguanidine compounds as trka kinase inhibitors |
SG11201503728XA SG11201503728XA (en) | 2012-11-13 | 2013-11-12 | N-pyrrolidinyl, n'-pyrazolyl- urea, thiourea, guanidine and cyanoguanidine compounds as trka kinase inhibitors |
US14/442,613 US9896435B2 (en) | 2012-11-13 | 2013-11-12 | N-pyrrolidinyl,N′-pyrazolyl-urea, thiourea, guanidine and cyanoguanidine compounds as TrkA kinase inhibitors |
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JP2015542020A JP6316834B2 (en) | 2012-11-13 | 2013-11-12 | N-pyrrolidinyl, N'-pyrazolyl urea, thiourea, guanidine, and cyanoguanidine compounds as TRKA kinase inhibitors |
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BR112015010875-0A BR112015010875B1 (en) | 2012-11-13 | 2013-11-12 | N-PYRROLIDINYL, N-PYRAZOLYL-UREA, THIOUREA, GUANIDINE AND CYANOGUANIDINE COMPOUNDS AS TRKA KINASE INHIBITORS, THEIR PHARMACEUTICAL COMPOSITION, THEIR USE AND THEIR PROCESS FOR PREPARATION |
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US15/851,418 US10851080B2 (en) | 2012-11-13 | 2017-12-21 | Methods of treatment using pyrrolidinyl urea, thiourea, guanidine and cyanoguanidine compounds |
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Cited By (53)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US9546156B2 (en) | 2012-11-13 | 2017-01-17 | Array Biopharma Inc. | N-bicyclic aryl,N'-pyrazolyl urea, thiourea, guanidine cyanoguanidine compounds as TrkA kinase inhibitors |
WO2017011776A1 (en) | 2015-07-16 | 2017-01-19 | Array Biopharma, Inc. | Substituted pyrazolo[1,5-a]pyridine compounds as ret kinase inhibitors |
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US9782415B2 (en) | 2009-07-09 | 2017-10-10 | Array Biopharma, Inc. | Substituted pyrazolo[1,5-a]pyrimidine compounds as Trk kinase inhibitors |
US9782414B2 (en) | 2014-11-16 | 2017-10-10 | Array Biopharma, Inc. | Crystalline form of (S)-N-(5-((R)-2-(2,5-difluorophenyl)-pyrrolidin-1-yl)-pyrazolo[1,5-A]pyrimidin-3-yl)-3-hydroxypyrrolidine-1-carboxamide hydrogen sulfate |
WO2017176751A1 (en) | 2016-04-04 | 2017-10-12 | Loxo Oncology, Inc. | Liquid formulations of (s)-n-(5-((r)-2-(2,5-difluorophenyl)-pyrrolidin-1-yl)-pyrazolo[1,5-a]pyrimidin-3-yl)-3-hydroxypyrrolidine-1-carboxamide |
WO2017176744A1 (en) | 2016-04-04 | 2017-10-12 | Loxo Oncology, Inc. | Methods of treating pediatric cancers |
US9790210B2 (en) | 2012-11-13 | 2017-10-17 | Array Biopharma Inc. | N-(monocyclic aryl),N'-pyrazolyl-urea, thiourea, guanidine and cyanoguanidine compounds as TrkA kinase inhibitors |
US9790178B2 (en) | 2012-11-13 | 2017-10-17 | Array Biopharma Inc. | Pyrrolidinyl urea, thiourea, guanidine and cyanoguanidine compounds as TrkA kinase inhibitors |
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US9822069B2 (en) | 2013-11-28 | 2017-11-21 | Kyorin Pharmaceutical Co., Ltd. | Urea derivative or pharmacologically acceptable salt thereof |
US9822118B2 (en) | 2012-11-13 | 2017-11-21 | Array Biopharma Inc. | Bicyclic heteroaryl urea, thiourea, guanidine and cyanoguanidine compounds as TrkA kinase inhibitors |
US9828360B2 (en) | 2012-11-13 | 2017-11-28 | Array Biopharma Inc. | Pyrrolidinyl urea, thiourea, guanidine and cyanoguanidine compounds as TrkA kinase inhibitors |
US9896435B2 (en) | 2012-11-13 | 2018-02-20 | Array Biopharma Inc. | N-pyrrolidinyl,N′-pyrazolyl-urea, thiourea, guanidine and cyanoguanidine compounds as TrkA kinase inhibitors |
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WO2018071454A1 (en) | 2016-10-10 | 2018-04-19 | Andrews Steven W | Substituted pyrazolo[1,5-a]pyridine compounds as ret kinase inhibitors |
US9969694B2 (en) | 2012-11-13 | 2018-05-15 | Array Biopharma Inc. | N-(arylalkyl)-N′-pyrazolyl-urea, thiourea, guanidine and cyanoguanidine compounds as TrkA kinase inhibitors |
US9981959B2 (en) | 2012-11-13 | 2018-05-29 | Array Biopharma Inc. | Thiazolyl and oxazolyl urea, thiourea, guanidine and cyanoguanidine compounds as TrkA kinase inhibitors |
US10005783B2 (en) | 2008-10-22 | 2018-06-26 | Array Biopharma Inc. | Method of treatment using substituted pyrazolo[1,5-a] pyrimidine compounds |
WO2018136661A1 (en) | 2017-01-18 | 2018-07-26 | Andrews Steven W | SUBSTITUTED PYRAZOLO[1,5-a]PYRAZINE COMPOUNDS AS RET KINASE INHIBITORS |
WO2018136663A1 (en) | 2017-01-18 | 2018-07-26 | Array Biopharma, Inc. | Ret inhibitors |
US10045991B2 (en) | 2016-04-04 | 2018-08-14 | Loxo Oncology, Inc. | Methods of treating pediatric cancers |
WO2018170381A1 (en) | 2017-03-16 | 2018-09-20 | Andrews Steven W | Macrocyclic compounds as ros1 kinase inhibitors |
US10160727B2 (en) | 2014-08-06 | 2018-12-25 | Shionogi & Co., Ltd. | Heterocycle and carbocycle derivatives having TrkA inhibitory activity |
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Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
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Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2009140128A2 (en) * | 2008-05-13 | 2009-11-19 | Irm Llc | Compounds and compositions as kinase inhibitors |
WO2011006074A1 (en) * | 2009-07-09 | 2011-01-13 | Array Biopharma Inc. | SUBSTITUTED PYRAZOLO[1,5-a]PYRIMIDINE COMPOUNDS AS TRK KINASE INHIBITORS |
EP2336105A1 (en) * | 2008-09-19 | 2011-06-22 | Takeda Pharmaceutical Company Limited | Nitrogen-containing heterocyclic compound and use of same |
WO2012158413A2 (en) * | 2011-05-13 | 2012-11-22 | Array Biopharma Inc. | Pyrrolidinyl urea and pyrrolidinyl thiourea compounds as trka kinase inhibitors |
Family Cites Families (73)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
NZ299242A (en) | 1995-09-11 | 1997-12-19 | Nihon Nohyaku Co Ltd | N-phenyl-n'-(phenyl substituted imidazol-5-yl, -oxazol-4-yl, and -thiazol-4-yl)urea derivatives |
CA2206201A1 (en) | 1996-05-29 | 1997-11-29 | Yoshiaki Isobe | Pyrazole derivatives and their pharmaceutical use |
US6083986A (en) | 1996-07-26 | 2000-07-04 | Icagen, Inc. | Potassium channel inhibitors |
US5998424A (en) | 1997-06-19 | 1999-12-07 | Dupont Pharmaceuticals Company | Inhibitors of factor Xa with a neutral P1 specificity group |
JP2001521934A (en) | 1997-11-03 | 2001-11-13 | ベーリンガー インゲルハイム ファーマシューティカルズ インコーポレイテッド | Aromatic heterocyclic compounds as anti-inflammatory drugs |
US7329670B1 (en) | 1997-12-22 | 2008-02-12 | Bayer Pharmaceuticals Corporation | Inhibition of RAF kinase using aryl and heteroaryl substituted heterocyclic ureas |
ATE346600T1 (en) | 1997-12-22 | 2006-12-15 | Bayer Pharmaceuticals Corp | INHIBITION OF P38 KINASE ACTIVITY BY THE USE OF ARYL AND HETEROARYL SUBSTITUTED UREAS |
ATE529109T1 (en) | 1997-12-22 | 2011-11-15 | Bayer Healthcare Llc | INHIBITION OF P38 KINASE ACTIVITY BY SUBSTITUTED HETEROCYCLIC UREAS |
US6197798B1 (en) | 1998-07-21 | 2001-03-06 | Novartis Ag | Amino-benzocycloalkane derivatives |
ES2244231T3 (en) | 1998-12-25 | 2005-12-01 | Teikoku Hormone Mfg. Co., Ltd. | DERIVATIVES OF AMINOPIRAZOL. |
UA73492C2 (en) | 1999-01-19 | 2005-08-15 | Aromatic heterocyclic compounds as antiinflammatory agents | |
US6387900B1 (en) | 1999-08-12 | 2002-05-14 | Pharmacia & Upjohn S.P.A. | 3(5)-ureido-pyrazole derivatives process for their preparation and their use as antitumor agents |
US6410533B1 (en) | 2000-02-10 | 2002-06-25 | Genzyme Corporation | Antibacterial compounds |
WO2002002525A2 (en) | 2000-06-30 | 2002-01-10 | Bristol-Myers Squibb Pharma Company | N-ureidoheterocycloaklyl-piperidines as modulators of chemokine receptor activity |
JP2004534017A (en) | 2001-04-27 | 2004-11-11 | バーテックス ファーマシューティカルズ インコーポレイテッド | BACE inhibitors |
GB0110901D0 (en) | 2001-05-02 | 2001-06-27 | Smithkline Beecham Plc | Novel Compounds |
ATE455104T1 (en) | 2001-11-01 | 2010-01-15 | Icagen Inc | PYRAZOLAMIDE FOR USE IN THE TREATMENT OF PAIN |
AU2002352868A1 (en) | 2001-11-27 | 2003-06-10 | Merck & Co., Inc. | 4-aminoquinoline compounds |
SE0104248D0 (en) | 2001-12-14 | 2001-12-14 | Astrazeneca Ab | Method of treatment |
CN1678608A (en) | 2002-07-02 | 2005-10-05 | 先灵公司 | New neuropeptide y y5 receptor antagonists |
CA2501626A1 (en) | 2002-10-08 | 2004-04-22 | Rinat Neuroscience Corp. | Methods for treating post-surgical pain by administering a nerve growth factor antagonist and compositions containing the same |
US20040171075A1 (en) | 2002-12-31 | 2004-09-02 | Flynn Daniel L | Modulation of protein functionalities |
US7202257B2 (en) | 2003-12-24 | 2007-04-10 | Deciphera Pharmaceuticals, Llc | Anti-inflammatory medicaments |
WO2005024755A2 (en) | 2002-12-31 | 2005-03-17 | Deciphera Pharmaceuticals, Llc. | Medicaments for the treatment of neurodegenerative disorders or diabetes |
US7144911B2 (en) | 2002-12-31 | 2006-12-05 | Deciphera Pharmaceuticals Llc | Anti-inflammatory medicaments |
PL2017265T3 (en) | 2003-06-12 | 2011-11-30 | Abbvie Inc | Fused compounds that inhibit vanilloid receptor subtype 1 (VR1) receptor |
CA2545711A1 (en) | 2003-11-13 | 2005-06-02 | Ambit Biosciences Corporation | Urea derivatives as kinase modulators |
US20080220497A1 (en) | 2003-12-24 | 2008-09-11 | Flynn Daniel L | Modulation of protein functionalities |
JP4573223B2 (en) | 2004-01-23 | 2010-11-04 | 東レ・ファインケミカル株式会社 | Process for producing optically active trans-4-amino-1-benzyl-3-pyrrolidinol |
CA2564325A1 (en) | 2004-04-30 | 2005-11-24 | Bayer Pharmaceuticals Corporation | Substituted pyrazolyl urea derivatives useful in the treatment of cancer |
JP2008524213A (en) | 2004-12-20 | 2008-07-10 | アストラゼネカ・アクチエボラーグ | Novel pyrazole derivatives and their use as modulators of nicotinic acetylcholine receptors |
EP1835934A4 (en) | 2004-12-23 | 2010-07-28 | Deciphera Pharmaceuticals Llc | Enzyme modulators and treatments |
US20090312349A1 (en) | 2004-12-23 | 2009-12-17 | Deciphera Pharmaceuticals, Llc | Anti-inflammatory medicaments |
WO2006070198A1 (en) | 2004-12-30 | 2006-07-06 | Astex Therapeutics Limited | Pyrazole derivatives as that modulate the activity of cdk, gsk and aurora kinases |
WO2010104488A1 (en) | 2009-02-19 | 2010-09-16 | University Of Connecticut | Novel hetero pyrrole analogs acting on cannapinoid receptors |
GB0510141D0 (en) | 2005-05-18 | 2005-06-22 | Addex Pharmaceuticals Sa | Novel compounds B3 |
EP1960394A2 (en) | 2005-11-15 | 2008-08-27 | Bayer HealthCare AG | Pyrazolyl urea derivatives useful in the treatment of cancer |
US7514435B2 (en) | 2005-11-18 | 2009-04-07 | Bristol-Myers Squibb Company | Pyrrolotriazine kinase inhibitors |
US20110195110A1 (en) | 2005-12-01 | 2011-08-11 | Roger Smith | Urea compounds useful in the treatment of cancer |
WO2008016811A2 (en) | 2006-07-31 | 2008-02-07 | Neurogen Corporation | Aminopiperidines and realted compounds |
EP2049542B1 (en) | 2006-08-09 | 2012-09-19 | Bristol-Myers Squibb Company | Pyrrolotriazine kinase inhibitors |
US7897762B2 (en) | 2006-09-14 | 2011-03-01 | Deciphera Pharmaceuticals, Llc | Kinase inhibitors useful for the treatment of proliferative diseases |
US8188113B2 (en) | 2006-09-14 | 2012-05-29 | Deciphera Pharmaceuticals, Inc. | Dihydropyridopyrimidinyl, dihydronaphthyidinyl and related compounds useful as kinase inhibitors for the treatment of proliferative diseases |
US7790756B2 (en) | 2006-10-11 | 2010-09-07 | Deciphera Pharmaceuticals, Llc | Kinase inhibitors useful for the treatment of myleoproliferative diseases and other proliferative diseases |
BRPI0807717A2 (en) | 2007-04-20 | 2014-05-20 | Deciphera Pharmaceuticals Llc | KINASE INHIBITORS USEFUL FOR TREATMENT OF MYELOPROLIFERATIVE DISEASES AND OTHER PROLIFERATIVE DISEASES. |
WO2008150899A1 (en) | 2007-05-29 | 2008-12-11 | Emory University | Combination therapies for treatment of cancer and inflammatory diseases |
ITMI20071731A1 (en) | 2007-09-06 | 2009-03-07 | Univ Degli Studi Genova | NEW UREIC DERIVATIVES OF 1H-PIRAZOL-4-CARBOXYLIC ACID WITH INHIBITIVE ACTIVITY TOWARDS NEUTRROPHILES CHEMOTASSASSES |
CA2952692C (en) | 2008-09-22 | 2020-04-28 | Array Biopharma Inc. | Substituted imidazo[1,2b]pyridazine compounds |
CN102177136A (en) | 2008-10-09 | 2011-09-07 | 弗·哈夫曼-拉罗切有限公司 | Pyrrolidine N-benzyl derivatives |
HUE037716T2 (en) | 2008-10-22 | 2018-09-28 | Array Biopharma Inc | Substituted pyrazolo[1,5-]pyrimidine compounds as trk kinase inhibitors |
AU2009316710B2 (en) | 2008-11-19 | 2015-08-06 | Boehringer Ingelheim Animal Health USA Inc. | Dimeric 1-arylpyrazole derivatives |
BRPI0922224A2 (en) | 2008-12-08 | 2016-08-02 | Vm Pharma Llc | receptor protein tyrosine kinase inhibitor compositions. |
JP2012513409A (en) | 2008-12-23 | 2012-06-14 | アボット・ラボラトリーズ | Antiviral compounds |
EP2426135A4 (en) | 2009-04-27 | 2013-02-20 | Shionogi & Co | Urea derivative having pi3k inhibitory activity |
WO2011032291A1 (en) | 2009-09-18 | 2011-03-24 | Zalicus Pharmaceuticals Ltd . | Selective calcium channel modulators |
MY191934A (en) | 2010-05-20 | 2022-07-19 | Array Biopharma Inc | Macrocyclic compounds as trk kinase inhibitors |
WO2012129258A1 (en) * | 2011-03-22 | 2012-09-27 | Merck Sharp & Dohme Corp. | Amidopyrazole inhibitors of interleukin receptor-associated kinases |
WO2013063214A1 (en) | 2011-10-27 | 2013-05-02 | Merck Sharp & Dohme Corp. | Novel compounds that are erk inhibitors |
US8969325B2 (en) | 2011-12-19 | 2015-03-03 | Abbvie Inc. | TRPV1 antagonists |
EP2858501A4 (en) | 2012-05-22 | 2015-12-09 | Merck Sharp & Dohme | TrkA KINASE INHIBITORS, COMPOSITIONS AND METHODS THEREOF |
EP2900223B1 (en) | 2012-09-28 | 2017-10-25 | Merck Sharp & Dohme Corp. | Novel compounds that are erk inhibitors |
CN105050598B (en) | 2012-09-28 | 2018-04-27 | 默沙东公司 | New compound as ERK inhibitor |
MX365733B (en) | 2012-11-13 | 2019-06-12 | Array Biopharma Inc | N-pyrrolidinyl, n'-pyrazolyl- urea, thiourea, guanidine and cyanoguanidine compounds as trka kinase inhibitors. |
US9828360B2 (en) | 2012-11-13 | 2017-11-28 | Array Biopharma Inc. | Pyrrolidinyl urea, thiourea, guanidine and cyanoguanidine compounds as TrkA kinase inhibitors |
US9546156B2 (en) | 2012-11-13 | 2017-01-17 | Array Biopharma Inc. | N-bicyclic aryl,N'-pyrazolyl urea, thiourea, guanidine cyanoguanidine compounds as TrkA kinase inhibitors |
US9981959B2 (en) | 2012-11-13 | 2018-05-29 | Array Biopharma Inc. | Thiazolyl and oxazolyl urea, thiourea, guanidine and cyanoguanidine compounds as TrkA kinase inhibitors |
US9790178B2 (en) | 2012-11-13 | 2017-10-17 | Array Biopharma Inc. | Pyrrolidinyl urea, thiourea, guanidine and cyanoguanidine compounds as TrkA kinase inhibitors |
RS55593B1 (en) | 2012-11-13 | 2017-06-30 | Array Biopharma Inc | Bicyclic urea, thiourea, guanidine and cyanoguanidine compounds useful for the treatment of pain |
WO2014078325A1 (en) | 2012-11-13 | 2014-05-22 | Array Biopharma Inc. | N-(monocyclic aryl),n'-pyrazolyl-urea, thiourea, guanidine and cyanoguanidine compounds as trka kinase inhibitors |
US9822118B2 (en) | 2012-11-13 | 2017-11-21 | Array Biopharma Inc. | Bicyclic heteroaryl urea, thiourea, guanidine and cyanoguanidine compounds as TrkA kinase inhibitors |
WO2014078417A1 (en) | 2012-11-13 | 2014-05-22 | Array Biopharma Inc. | Pyrazolyl urea, thiourea, guanidine and cyanoguanidine compounds as trka kinase inhibitors |
WO2014078331A1 (en) | 2012-11-13 | 2014-05-22 | Array Biopharma Inc. | N-(arylalkyl)-n'-pyrazolyl-urea, thiourea, guanidine and cyanoguanidine compounds as trka kinase inhibitors |
WO2015039333A1 (en) | 2013-09-22 | 2015-03-26 | Merck Sharp & Dohme Corp. | TrkA KINASE INHIBITORS, COMPOSITIONS AND METHODS THEREOF |
-
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Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2009140128A2 (en) * | 2008-05-13 | 2009-11-19 | Irm Llc | Compounds and compositions as kinase inhibitors |
EP2336105A1 (en) * | 2008-09-19 | 2011-06-22 | Takeda Pharmaceutical Company Limited | Nitrogen-containing heterocyclic compound and use of same |
WO2011006074A1 (en) * | 2009-07-09 | 2011-01-13 | Array Biopharma Inc. | SUBSTITUTED PYRAZOLO[1,5-a]PYRIMIDINE COMPOUNDS AS TRK KINASE INHIBITORS |
WO2012158413A2 (en) * | 2011-05-13 | 2012-11-22 | Array Biopharma Inc. | Pyrrolidinyl urea and pyrrolidinyl thiourea compounds as trka kinase inhibitors |
Non-Patent Citations (1)
Title |
---|
WANG T ET AL: "Trk kinase inhibitors as new treatments for cancer and pain", EXPERT OPINION ON THERAPEUTIC PATENTS, INFORMA HEALTHCARE, GB, vol. 19, no. 3, 1 March 2009 (2009-03-01), pages 305 - 319, XP002557234, ISSN: 1354-3776, DOI: 10.1517/13543770902721261 * |
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---|---|---|---|---|
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US11267818B2 (en) | 2008-10-22 | 2022-03-08 | Array Biopharma Inc. | Method of treatment using substituted pyrazolo[1,5-a] pyrimidine compounds |
US9796724B2 (en) | 2009-07-09 | 2017-10-24 | Array Biopharma, Inc. | Substituted pyrazolo[1,5-a]pyrimidine compounds as Trk kinase inhibitors |
US10251889B2 (en) | 2009-07-09 | 2019-04-09 | Array BioPharm Inc. | Substituted pyrazolo[1,5-a]pyrimidine compounds as Trk kinase inhibitors |
US9782415B2 (en) | 2009-07-09 | 2017-10-10 | Array Biopharma, Inc. | Substituted pyrazolo[1,5-a]pyrimidine compounds as Trk kinase inhibitors |
US10758542B2 (en) | 2009-07-09 | 2020-09-01 | Array Biopharma Inc. | Substituted pyrazolo[l,5-a]pyrimidine compounds as Trk kinase inhibitors |
US9840519B2 (en) | 2010-05-20 | 2017-12-12 | Array Biopharma, Inc. | Macrocyclic compounds as TRK kinase inhibitors |
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US9718822B2 (en) | 2010-05-20 | 2017-08-01 | Array Biopharma, Inc. | Macrocyclic compounds as Trk kinase inhibitors |
US9750744B2 (en) | 2010-05-20 | 2017-09-05 | Array Biopharma, Inc. | Macrocyclic compounds as Trk kinase inhibitors |
US9902741B2 (en) | 2010-05-20 | 2018-02-27 | Array Biopharma Inc. | Macrocyclic compounds as TRK kinase inhibitors |
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US10323022B2 (en) | 2011-05-13 | 2019-06-18 | Array Biopharma Inc. | Pyrrolidinyl urea, pyrrolidinyl thiourea and pyrrolidinyl guanidine compounds as TrkA kinase inhibitors |
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US9790210B2 (en) | 2012-11-13 | 2017-10-17 | Array Biopharma Inc. | N-(monocyclic aryl),N'-pyrazolyl-urea, thiourea, guanidine and cyanoguanidine compounds as TrkA kinase inhibitors |
US9896435B2 (en) | 2012-11-13 | 2018-02-20 | Array Biopharma Inc. | N-pyrrolidinyl,N′-pyrazolyl-urea, thiourea, guanidine and cyanoguanidine compounds as TrkA kinase inhibitors |
US9828360B2 (en) | 2012-11-13 | 2017-11-28 | Array Biopharma Inc. | Pyrrolidinyl urea, thiourea, guanidine and cyanoguanidine compounds as TrkA kinase inhibitors |
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US9782414B2 (en) | 2014-11-16 | 2017-10-10 | Array Biopharma, Inc. | Crystalline form of (S)-N-(5-((R)-2-(2,5-difluorophenyl)-pyrrolidin-1-yl)-pyrazolo[1,5-A]pyrimidin-3-yl)-3-hydroxypyrrolidine-1-carboxamide hydrogen sulfate |
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US10640495B2 (en) | 2015-07-07 | 2020-05-05 | Shionogi & Co., Ltd. | Heterocycle derivatives having TrkA inhibitory activity |
US10138243B2 (en) | 2015-07-16 | 2018-11-27 | Array Biopharma Inc. | Substituted pyrazolo[1,5-a]pyridine compounds as RET kinase inhibitors |
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US10174027B2 (en) | 2015-07-16 | 2019-01-08 | Array Biopharma Inc. | Substituted pyrazolo[1,5-a]pyridine compounds as RET kinase inhibitors |
US10655186B2 (en) | 2015-10-26 | 2020-05-19 | Loxo Oncology, Inc. | Point mutations in TRK inhibitor-resistant cancer and methods relating to the same |
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WO2017075107A1 (en) | 2015-10-26 | 2017-05-04 | Nanda Nisha | Point mutations in trk inhibitor-resistant cancer and methods relating to the same |
US10370727B2 (en) | 2015-10-26 | 2019-08-06 | Loxo Oncology, Inc. | Point mutations in TRK inhibitor-resistant cancer and methods relating to the same |
US10378068B2 (en) | 2015-10-26 | 2019-08-13 | Loxo Oncology, Inc. | Point mutations in TRK inhibitor-resistant cancer and methods relating to the same |
US10724102B2 (en) | 2015-10-26 | 2020-07-28 | Loxo Oncology, Inc. | Point mutations in TRK inhibitor-resistant cancer and methods relating to the same |
US10781210B2 (en) | 2016-02-04 | 2020-09-22 | Shionogi & Co., Ltd. | Nitrogen-containing heterocycle and carbocycle derivatives having TrkA inhibitory activity |
US11008320B2 (en) | 2016-02-04 | 2021-05-18 | Shionogi & Co., Ltd. | Nitrogen-containing heterocycle and carbocycle derivatives having TrkA inhibitory activity |
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US10533006B2 (en) | 2016-02-04 | 2020-01-14 | Shionogi & Co., Ltd. | Nitrogen-containing heterocycle and carbocycle derivatives having TrkA inhibitory activity |
JPWO2017135399A1 (en) * | 2016-02-04 | 2018-11-29 | 塩野義製薬株式会社 | Nitrogen-containing heterocyclic and carbocyclic derivatives having TrkA inhibitory activity |
WO2017176751A1 (en) | 2016-04-04 | 2017-10-12 | Loxo Oncology, Inc. | Liquid formulations of (s)-n-(5-((r)-2-(2,5-difluorophenyl)-pyrrolidin-1-yl)-pyrazolo[1,5-a]pyrimidin-3-yl)-3-hydroxypyrrolidine-1-carboxamide |
WO2017176744A1 (en) | 2016-04-04 | 2017-10-12 | Loxo Oncology, Inc. | Methods of treating pediatric cancers |
US11484535B2 (en) | 2016-04-04 | 2022-11-01 | Loxo Oncology, Inc. | Liquid formulations of (S)-N-(5-((R)-2-(2,5-difluorophenyl)-pyrrolidin-1-yl)-pyrazolo[1,5-a] pyrimidin-3-yl)-3-hydroxypyrrolidine-1-carboxamide |
US10668072B2 (en) | 2016-04-04 | 2020-06-02 | Loxo Oncology, Inc. | Liquid formulations of (S)-N-(5-((R)-2-(2,5-difluorophenyl)-pyrrolidin-1-yl)-pyrazolo[1,5-a]pyrimidin-3-yl)-3-hydroxypyrrolidine-1-carboxamide |
US10588908B2 (en) | 2016-04-04 | 2020-03-17 | Loxo Oncology, Inc. | Methods of treating pediatric cancers |
US10045991B2 (en) | 2016-04-04 | 2018-08-14 | Loxo Oncology, Inc. | Methods of treating pediatric cancers |
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US10137127B2 (en) | 2016-04-04 | 2018-11-27 | Loxo Oncology, Inc. | Liquid formulations of (S)-N-(5-((R)-2-(2,5-difluorophenyl)-pyrrolidin-1-yl)-pyrazolo[1,5-A]pyrimidin-3-yl)-3-hydroxypyrrolidine-1-carboxamide |
US11214571B2 (en) | 2016-05-18 | 2022-01-04 | Array Biopharma Inc. | Process for the preparation of (S)-N-(5-((R)-2-(2,5-difluorophenyl)pyrrolidin-1-yl)-pyrazolo[1,5-a]pyrimidin-3-yl)-3-hydroxypyrrolidine-1-carboxamide and salts thereof |
US10441581B2 (en) | 2016-10-10 | 2019-10-15 | Array Biopharma Inc. | Substituted pyrazolo[1,5-A]pyridine compounds as RET kinase inhibitors |
US10144734B2 (en) | 2016-10-10 | 2018-12-04 | Array Biopharma Inc. | Substituted pyrazolo[1,5-A]pyridine compounds as RET kinase inhibitors |
US10555944B2 (en) | 2016-10-10 | 2020-02-11 | Eli Lilly And Company | Substituted pyrazolo[1,5-A]pyridine compounds as RET kinase inhibitors |
US11998545B2 (en) | 2016-10-10 | 2024-06-04 | Array Biopharma Inc. | Substituted pyrazolo[1,5-a]pyridine compounds as RET kinase inhibitors |
US10112942B2 (en) | 2016-10-10 | 2018-10-30 | Array Biopharma Inc. | Substituted pyrazolo[1,5-A]pyridine compounds as RET kinase inhibitors |
US10953005B1 (en) | 2016-10-10 | 2021-03-23 | Array Biopharma Inc. | Substituted pyrazolo[1,5-a]pyridine compounds as RET kinase inhibitors |
US10137124B2 (en) | 2016-10-10 | 2018-11-27 | Array Biopharma Inc. | Substituted pyrazolo[1,5-a]pyridine compounds as RET kinase inhibitors |
US10172845B2 (en) | 2016-10-10 | 2019-01-08 | Array Biopharma Inc. | Substituted pyrazolo[1,5-A]pyridine compounds as RET kinase inhibitors |
US11648243B2 (en) | 2016-10-10 | 2023-05-16 | Array Biopharma Inc. | Substituted pyrazolo[1,5-A]pyridine compounds as RET kinase inhibitors |
EP4144735A1 (en) | 2016-10-10 | 2023-03-08 | Array Biopharma, Inc. | Substituted pyrazolo[1,5-a]pyridine compounds as ret kinase inhibitors |
WO2018071447A1 (en) | 2016-10-10 | 2018-04-19 | Andrews Steven W | Substituted pyrazolo[1,5-a]pyridine compounds as ret kinase inhibitors |
WO2018071454A1 (en) | 2016-10-10 | 2018-04-19 | Andrews Steven W | Substituted pyrazolo[1,5-a]pyridine compounds as ret kinase inhibitors |
US10881652B2 (en) | 2016-10-10 | 2021-01-05 | Array Biopharma Inc. | Substituted pyrazolo[1,5-A]pyridine compounds as RET kinase inhibitors |
US10172851B2 (en) | 2016-10-10 | 2019-01-08 | Array Biopharma Inc. | Substituted pyrazolo[1,5-A]pyridine compounds as RET kinase inhibitors |
EP3753939A1 (en) | 2016-10-10 | 2020-12-23 | Array Biopharma Inc. | Substituted pyrazolo[1,5-a]pyridine compounds as ret kinase inhibitors |
US11091486B2 (en) | 2016-10-26 | 2021-08-17 | Array Biopharma, Inc | Process for the preparation of pyrazolo[1,5-a]pyrimidines and salts thereof |
WO2018136663A1 (en) | 2017-01-18 | 2018-07-26 | Array Biopharma, Inc. | Ret inhibitors |
WO2018136661A1 (en) | 2017-01-18 | 2018-07-26 | Andrews Steven W | SUBSTITUTED PYRAZOLO[1,5-a]PYRAZINE COMPOUNDS AS RET KINASE INHIBITORS |
US11851434B2 (en) | 2017-01-18 | 2023-12-26 | Array Biopharma Inc. | Substituted pyrazolo[1,5-A]pyrazine compounds as ret kinase inhibitors |
US11168090B2 (en) | 2017-01-18 | 2021-11-09 | Array Biopharma Inc. | Substituted pyrazolo[1,5-a]pyrazines as RET kinase inhibitors |
WO2018170381A1 (en) | 2017-03-16 | 2018-09-20 | Andrews Steven W | Macrocyclic compounds as ros1 kinase inhibitors |
US10966985B2 (en) | 2017-03-16 | 2021-04-06 | Array Biopharma Inc. | Macrocyclic compounds as ROS1 kinase inhibitors |
US10688100B2 (en) | 2017-03-16 | 2020-06-23 | Array Biopharma Inc. | Macrocylic compounds as ROS1 kinase inhibitors |
WO2019065954A1 (en) | 2017-09-29 | 2019-04-04 | 田辺三菱製薬株式会社 | Optically active pyrrolidine compound and method for producing same |
EP4273141A1 (en) | 2017-09-29 | 2023-11-08 | Mitsubishi Tanabe Pharma Corporation | Optically active pyrrolidine compound and method for producing same |
US11845738B2 (en) | 2017-09-29 | 2023-12-19 | Mitsubishi Tanabe Pharma Corporation | Optically active pyrrolidine compound and method for producing same |
US11053217B2 (en) | 2017-09-29 | 2021-07-06 | Mitsubishi Tanabe Pharma Corporation | Optically active pyrrolidine compound and method for producing same |
WO2019075108A1 (en) | 2017-10-10 | 2019-04-18 | Metcalf Andrew T | Crystalline forms |
WO2019075114A1 (en) | 2017-10-10 | 2019-04-18 | Mark Reynolds | Formulations comprising 6-(2-hydroxy-2-methylpropoxy)-4-(6-(6-((6-methoxypyridin-3-yl)methyl)-3,6-diazab icyclo[3.1.1]heptan-3-yl)pyridin-3-yl)pyrazolo[1,5-a]pyridine-3-carbonitrile |
WO2019084285A1 (en) | 2017-10-26 | 2019-05-02 | Qian Zhao | Formulations of a macrocyclic trk kinase inhibitor |
WO2019143977A1 (en) | 2018-01-18 | 2019-07-25 | Array Biopharma Inc. | Substituted pyrrolo[2,3-d]pyrimidines compounds as ret kinase inhibitors |
US11472802B2 (en) | 2018-01-18 | 2022-10-18 | Array Biopharma Inc. | Substituted pyrazolyl[4,3-c]pyridine compounds as RET kinase inhibitors |
US11603374B2 (en) | 2018-01-18 | 2023-03-14 | Array Biopharma Inc. | Substituted pyrrolo[2,3-d]pyrimidines compounds as ret kinase inhibitors |
US11524963B2 (en) | 2018-01-18 | 2022-12-13 | Array Biopharma Inc. | Substituted pyrazolo[3,4-d]pyrimidines as RET kinase inhibitors |
WO2019143994A1 (en) | 2018-01-18 | 2019-07-25 | Array Biopharma Inc. | Substituted pyrazolyl[4,3-c]pyridinecompounds as ret kinase inhibitors |
US11708327B2 (en) | 2018-03-05 | 2023-07-25 | Bristol-Myers Squibb Company | Phenylpyrrolidinone formyl peptide 2 receptor agonists |
US11117861B2 (en) | 2018-03-05 | 2021-09-14 | Bristol-Myers Squibb Company | Phenylpyrrolidinone formyl peptide 2 receptor agonists |
US10676431B2 (en) | 2018-03-05 | 2020-06-09 | Bristol-Myers Squibb Company | Phenylpyrrolidinone formyl peptide 2 receptor agonists |
WO2019191659A1 (en) | 2018-03-29 | 2019-10-03 | Loxo Oncology, Inc. | Treatment of trk-associated cancers |
EP3822266A4 (en) * | 2018-07-12 | 2022-04-27 | Zhangzhou Pien Tze Huang Pharmaceutical Co., Ltd | Pyrrolidinyl urea derivatives and application thereof in trka-related diseases |
US11932652B2 (en) | 2018-07-12 | 2024-03-19 | Zhangzhou Pien Tze Huang Pharmaceutical Co., Ltd. | Pyrrolidinyl urea derivatives and application thereof in TrkA-related diseases |
WO2020028258A1 (en) | 2018-07-31 | 2020-02-06 | Loxo Oncology, Inc. | Spray-dried dispersions and formulations of (s)-5-amino-3-(4-((5-fluoro-2-methoxybenzamido)methyl)phenyl)-1-(1,1,1-trifluoro propan-2-yl)-1h-pyrazole-4-carboxamide |
US11964988B2 (en) | 2018-09-10 | 2024-04-23 | Array Biopharma Inc. | Fused heterocyclic compounds as RET kinase inhibitors |
WO2020055672A1 (en) | 2018-09-10 | 2020-03-19 | Array Biopharma Inc. | Fused heterocyclic compounds as ret kinase inhibitors |
WO2020131674A1 (en) | 2018-12-19 | 2020-06-25 | Array Biopharma Inc. | 7-((3,5-dimethoxyphenyl)amino)quinoxaline derivatives as fgfr inhibitors for treating cancer |
WO2020131627A1 (en) | 2018-12-19 | 2020-06-25 | Array Biopharma Inc. | Substituted pyrazolo[1,5-a]pyridine compounds as inhibitors of fgfr tyrosine kinases |
WO2020188015A1 (en) | 2019-03-21 | 2020-09-24 | Onxeo | A dbait molecule in combination with kinase inhibitor for the treatment of cancer |
WO2021089791A1 (en) | 2019-11-08 | 2021-05-14 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Methods for the treatment of cancers that have acquired resistance to kinase inhibitors |
WO2021148581A1 (en) | 2020-01-22 | 2021-07-29 | Onxeo | Novel dbait molecule and its use |
CN114031556B (en) * | 2021-11-08 | 2023-03-31 | 温州大学 | Synthetic method for preparing 5-amino-N-aryl-3-arylpyrazole compound by green one-pot method |
CN114031556A (en) * | 2021-11-08 | 2022-02-11 | 温州大学 | Synthetic method for preparing 5-amino-N-aryl-3-arylpyrazole compound by green one-pot method |
WO2024061768A1 (en) | 2022-09-19 | 2024-03-28 | Basf Se | Azole pesticidal compounds |
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