WO2012177606A1 - Azetidinyl phenyl, pyridyl or pyrazinyl carboxamide derivatives as jak inhibitors - Google Patents

Azetidinyl phenyl, pyridyl or pyrazinyl carboxamide derivatives as jak inhibitors Download PDF

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Publication number
WO2012177606A1
WO2012177606A1 PCT/US2012/043099 US2012043099W WO2012177606A1 WO 2012177606 A1 WO2012177606 A1 WO 2012177606A1 US 2012043099 W US2012043099 W US 2012043099W WO 2012177606 A1 WO2012177606 A1 WO 2012177606A1
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Prior art keywords
alkyl
pyrazol
pyrrolo
cyanomethyl
pyrimidin
Prior art date
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Ceased
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PCT/US2012/043099
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English (en)
French (fr)
Inventor
Wenqing Yao
David M. Burns
Jincong Zhuo
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Incyte Corp
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Incyte Corp
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Filing date
Publication date
Priority to EP12735369.6A priority Critical patent/EP2721028B1/en
Priority to CN201280037078.XA priority patent/CN103797010B/zh
Priority to PH1/2013/502612A priority patent/PH12013502612A1/en
Priority to UAA201400439A priority patent/UA110978C2/uk
Priority to BR112013032720A priority patent/BR112013032720A2/pt
Priority to KR1020147001320A priority patent/KR20140040819A/ko
Priority to JP2014517080A priority patent/JP5876146B2/ja
Priority to AU2012273164A priority patent/AU2012273164B2/en
Priority to EA201490042A priority patent/EA201490042A1/ru
Application filed by Incyte Corp filed Critical Incyte Corp
Priority to MX2013015087A priority patent/MX344479B/es
Priority to ES12735369.6T priority patent/ES2560611T3/es
Priority to HK14110258.0A priority patent/HK1197056B/en
Priority to CA2839767A priority patent/CA2839767A1/en
Priority to NZ618982A priority patent/NZ618982B2/en
Publication of WO2012177606A1 publication Critical patent/WO2012177606A1/en
Priority to IL230008A priority patent/IL230008A/en
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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    • C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04—Ortho-condensed systems
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04—Ortho-condensed systems
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    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
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Definitions

  • Y is CR 7 .
  • R 1 is isopropyl, ethyl, 1 -methylpropyl, 2,2,2-trifluoro- 1-methylethyl, 1-cyclopropylethyl, 1 -cyclohexylethyl, cyclopropyl, 1- trifluoromethylcyclopropyl, 3,3-difluorocyclobutyl, or l-(l-methylpiperidin-4- yl)ethyl.
  • R 1 is isopropyl
  • R 1 is 1 -trifluoromethylcyclopropyl.
  • R 1 is 2,2,2-trifluoroethyl.
  • the compound is a compound of Formula IVa:
  • the compound has Formula Ilia, wherein R 1 , R 2 , R 3 , R 5 , R 6 are defined as in embodiment (a).
  • the compound has Formula IVa, wherein R 1 , R 2 , R 3 , and R 5 are defined as in embodiment (a).
  • the compound has Formula Illb, wherein R 1 , R 2 , R 3 , R 5 , R 6 are defined as in embodiment (b).
  • Resolution of racemic mixtures can also be carried out by elution on a column packed with an optically active resolving agent (e.g., dinitrobenzoylphenylglycine).
  • Suitable elution solvent composition can be determined by one skilled in the art.
  • Compounds of the invention also include tautomeric forms. Tautomeric forms result from the swapping of a single bond with an adjacent double bond together with the concomitant migration of a proton. Tautomeric forms include prototropic tautomers which are isomeric protonation states having the same empirical formula and total charge.
  • amine derivative 8 which can be converted to the corresponding aryl ester 10 by reaction with halo-substituted arylacid ester 9 in the presence of the suitable catalyst such as, but not limited to, ⁇ [2,2'-bis(diphenylphosphino)-l, l 'binaphthalene], Tol- ⁇ [2,2'-bis(di-p-tolylphosphino)-l, l 'binaphthalene], Xanthpos [4,5- bis(diphenylphosphino)-9,9-dimethylxanthene].
  • the suitable catalyst such as, but not limited to, ⁇ [2,2'-bis(diphenylphosphino)-l, l 'binaphthalene], Tol- ⁇ [2,2'-bis(di-p-tolylphosphino)-l, l 'binaphthalene], Xanthpos [4,5- bis(diphenylphosphino)-9,9
  • aryl amide derivatives 12 can be prepared according to the procedures outlined in Scheme 4.
  • the aryl ester 16 can be hydrolyzed to the corresponding acid 19 by using an alkali such as lithium hydroxide, sodium hydroxide or potassium hydroxide.
  • the acid 19 can be transfered to the arylamide 20 by reaction with an appropriate amine in the presence of a suitable coupling reagent such as, but not limited to, BOP, PyOP, HATU, HBTU, EDC, or CDI.
  • Swern oxidation of 20 can produce the corresponding ketone 21 which can be converted to the ⁇ , ⁇ - unsaturated nitrile 22 by Wittig's reaction with diethyl cyanomethylphosphonate.
  • Michael addition of 5 with ⁇ , ⁇ -unsaturated nitrile 21 can afford the adduct 12.
  • the JAK inhibitors described herein can further be used to treat ischemia reperfusion injuries or a disease or condition related to an inflammatory ischemic event such as stroke or cardiac arrest.
  • the JAK inhibitors described herein can further be used to treat endotoxin-driven disease state (e.g., complications after bypass surgery or chronic endotoxin states contributing to chronic cardiac failure).
  • the JAK inhibitors described herein can further be used to treat anorexia, cachexia, or fatigue such as that resulting from or associated with cancer.
  • the JAK inhibitors described herein can further be used to treat restenosis, sclerodermitis, or fibrosis.
  • treating or treatment refers to one or more of (1) inhibiting the disease; for example, inhibiting a disease, condition or disorder in an individual who is experiencing or displaying the pathology or symptomatology of the disease, condition or disorder (i.e., arresting further development of the pathology and/or symptomatology); and (2) ameliorating the disease; for example, ameliorating a disease, condition or disorder in an individual who is experiencing or displaying the pathology or symptomatology of the disease, condition or disorder (i.e., reversing the pathology and/or symptomatology) such as decreasing the severity of disease.
  • treating or treatment includes preventing the disease; for example, preventing a disease, condition or disorder in an individual who may be predisposed to the disease, condition or disorder but does not yet experience or display the pathology or symptomatology of the disease.
  • Example suitable RAF inhibitors include compounds, and their
  • the selectivity can be at least about 2-fold, at least about 3-fold, at least about 5-fold, at least about 10-fold, at least about 20-fold, at least about 50-fold, or at least about 100-fold. Potency can be measured by one or more in vitro assays, such as the assays provided below in the Examples.
  • the compositions of the invention contain from about 50 mg to about 500 mg of the active ingredient.
  • the active ingredient contains from about 50 mg to about 500 mg of the active ingredient.
  • One having ordinary skill in the art will appreciate that this embodies compounds or compositions containing about 50 mg to about 100 mg, about 100 mg to about 150 mg, about 150 mg to about 200 mg, about 200 mg to about 250 mg, about 250 mg to about 300 mg, about 350 mg to about 400 mg, or about 450 mg to about 500 mg of the active ingredient.
  • liquid forms in which the compounds and compositions of the present invention can be incorporated for administration orally or by injection include aqueous solutions, suitably flavored syrups, aqueous or oil suspensions, and flavored emulsions with edible oils such as cottonseed oil, sesame oil, coconut oil, or peanut oil, as well as elixirs and similar pharmaceutical vehicles.
  • compositions in can be nebulized by use of inert gases. Nebulized solutions may be breathed directly from the nebulizing device or the nebulizing device can be attached to a face masks tent, or intermittent positive pressure breathing machine. Solution, suspension, or powder compositions can be administered orally or nasally from devices which deliver the formulation in an appropriate manner.
  • the insert comprises a polymer selected from polyvinylpyrrolidone (PVP), an acrylate or methacrylate polymer or copolymer (e.g., Eudragit® family of polymers from Rohm or Degussa), hydroxymethyl cellulose, polyacrylic acid, poly(amidoamine) dendrimers, poly(dimethyl siloxane), polyethylene oxide, poly(lactide-co-glycolide), poly(2-hydroxyethylmethacrylate), poly(vinyl alcohol), or poly(propylene fumarate).
  • the insert comprises Gelfoam® R.
  • the insert is a polyacrylic acid of 450 kDa-cysteine conjugate.
  • Step 2 tert-butyl 3-(cyanomethylene)azetidine-l-carboxylate
  • Step 3 tert-butyl 3-(cyanomethyl)-3- [4-(l - ⁇ [2-(trimethylsilyl)ethoxy]methyl ⁇ - 1H- pyrrolo[2,3-b]pyridin-4-yl)-lH-pyrazol-l-yl]azetidine-l-carboxylate
  • Step 5 5- ⁇ 3-(cyanomethyl)-3-[4-(l- ⁇ [2-(trimethylsilyl)ethoxy]methyl ⁇ -lH- pyrrolo[2, 3-b]pyridin-4-yl)-lH-pyrazol-l-yl]azetidin-l-yl ⁇ -N-[ ( 1S)-1- cyclopropyle
  • Step 1 methyl 5- ⁇ 3-(cyanomethyl)-3-f4-(7- ⁇ f2-(trimethylsilyl)ethoxyJmethyl ⁇ -7H- pyrrolo[2,3-d]pyrimidin-4-yl)-lH-pyrazol-l-yl]azetidin-l-yl ⁇ pyrazine-2-carboxylate
  • Example 26 4- ⁇ 3-(Cyanomethyl)-3-[4-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)-lH- pyrazol-l-yl]azetidin-l-yl ⁇ -N-(2,2,2-trifluoro-l-methylethyl)benzamide
  • Step 3 4- ⁇ 3-(cyanomethyl)-3-[ 4-(7H-pyrrolo[2, 3-d]pyrimidin-4-yl)-lH-pyrazol-l- yl]azetidin-l-yl ⁇ -2,5-difluoro-N-[(lS)-2,2,2-trifluoro-l-methylethyl]benzamide
  • N,N-Diisopropylethylamine (0.11 mL, 0.62 mmol) was added to a mixture of ⁇ 3-[4-(7- ⁇ [2-(trimethylsilyl)ethoxy]methyl ⁇ -7H-pyrrolo[2,3-d]pyrimidin-4-yl)-lH- pyrazol-l-yl]azetidin-3-yl ⁇ acetonitrile dihydrochloride (110 mg, 0.22 mmol) and 5- chloro-N-[(lS)-2,2,2-trifluoro-l-methylethyl]pyrazine-2-carboxamide (52 mg, 0.21 mmol) in NMP (3.0 mL).
  • Step 3 5- ⁇ 3-(cyanomethyl)-3-[ 4-(7H-pyrrolo[2, 3-d]pyrimidin-4-yl)-lH-pyrazol-l- yl]azetidin-l-yl ⁇ -N-[(lS)-2,2,2-trifluoro-l-methylethyl]pyrazine-2-carboxamide
  • Step 1 5-chloro-N-[(lS)-l-cyclopropyl-2,2,2-trifluoroethyl]pyrazine-2-carboxamide N,N-Diisopropylethylamine (1.3 mL, 7.5 mmol) was added to a mixture of 5- chloropyrazine-2-carboxylic acid (0.40 g, 2.5 mmol), N,N,N',N'-tetramethyl-0-(7- azabenzotriazol-l-yl)uronium hexafluorophosphate (1.0 g, 2.8 mmol) and (lS)-l- cyclopropyl-2,2,2-trifluoroethanamine hydrochloride (0.44 g, 2.5 mmol) (ASIBA Pharmatech, Cat.#: 70092-HCl) in methylene chloride (10 mL).
  • N,N-Diisopropylethylamine (0.71 mL, 4.1 mmol) was added to a mixture of ⁇ 3-[4-(7- ⁇ [2-(trimethylsilyl)ethoxy]methyl ⁇ -7H-pyrrolo[2,3-d]pyrimidin-4-yl)-lH- pyrazol-l-yl]azetidin-3-yl ⁇ acetonitrile dihydrochloride (0.70 g, 1.4 mmol) and 5- chloro-N-[l-(trifluoromethyl)cyclopropyl]pyrazine-2-carboxamide (0.36 g, 1.4 mmol) in NMP (5.0 mL).
  • the above cell lines can also be used to examine the effects of compounds on phosphorylation of JAK kinases or potential downstream substrates such as STAT proteins, Akt, Shp2, or Erk. These experiments can be performed following an overnight cytokine starvation, followed by a brief preincubation with compound (2 hours or less) and cytokine stimulation of approximately 1 hour or less. Proteins are then extracted from cells and analyzed by techniques familiar to those schooled in the art including Western blotting or ELISAs using antibodies that can differentiate between phosphorylated and total protein. These experiments can utilize normal or cancer cells to investigate the activity of compounds on tumor cell survival biology or on mediators of inflammatory disease.

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PCT/US2012/043099 2011-06-20 2012-06-19 Azetidinyl phenyl, pyridyl or pyrazinyl carboxamide derivatives as jak inhibitors Ceased WO2012177606A1 (en)

Priority Applications (15)

Application Number Priority Date Filing Date Title
EA201490042A EA201490042A1 (ru) 2011-06-20 2012-06-19 Азетидинил-фенил-, пиридил- или пиразинилкарбоксамидные производные как ингибиторы jak
PH1/2013/502612A PH12013502612A1 (en) 2011-06-20 2012-06-19 Azetidinyl phenyl, pyridyl or pyrazinyl carboxamide derivatives as jak inhibitors
MX2013015087A MX344479B (es) 2011-06-20 2012-06-19 Derivados de azetidinil fenil, piridil o pirazinil carboxamida como inhibidores de cinasa janus (jak).
BR112013032720A BR112013032720A2 (pt) 2011-06-20 2012-06-19 "derivados de azetidinil fenil, piridil ou pirazinil carboxamida como inibidores de jak, composição e uso dos referidos derivados"
KR1020147001320A KR20140040819A (ko) 2011-06-20 2012-06-19 Ｊａｋ 저해제로서의 아제티디닐 페닐, 피리딜 또는 피라지닐 카르복스아미드 유도체
JP2014517080A JP5876146B2 (ja) 2011-06-20 2012-06-19 Ｊａｋ阻害剤としてのアゼチジニルフェニル、ピリジル、またはピラジニルカルボキサミド誘導体
AU2012273164A AU2012273164B2 (en) 2011-06-20 2012-06-19 Azetidinyl phenyl, pyridyl or pyrazinyl carboxamide derivatives as JAK inhibitors
EP12735369.6A EP2721028B1 (en) 2011-06-20 2012-06-19 Azetidinyl phenyl, pyridyl or pyrazinyl carboxamide derivatives as jak inhibitors
UAA201400439A UA110978C2 (uk) 2011-06-20 2012-06-19 Азетидинілфенілові, піридилові або піразинілкарбоксамідні похідні як інгібітори jak
CN201280037078.XA CN103797010B (zh) 2011-06-20 2012-06-19 作为jak抑制剂的氮杂环丁烷基苯基、吡啶基或吡嗪基甲酰胺衍生物
ES12735369.6T ES2560611T3 (es) 2011-06-20 2012-06-19 Derivados de fenil de azetidinilo, carboxamida de piridilo o pirazinilo como inhibidores de JAK
HK14110258.0A HK1197056B (en) 2011-06-20 2012-06-19 Azetidinyl phenyl, pyridyl or pyrazinyl carboxamide derivatives as jak inhibitors
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