Classifications

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  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
  • C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
  • C07D487/04—Ortho-condensed systems
• • A—HUMAN NECESSITIES
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  • A61P11/00—Drugs for disorders of the respiratory system
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  • A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
• • 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
• • 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
  • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
  • A61P31/12—Antivirals
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P35/00—Antineoplastic agents
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P35/00—Antineoplastic agents
  • A61P35/02—Antineoplastic agents specific for leukemia
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P9/00—Drugs for disorders of the cardiovascular system

Definitions

• PYRAZOLOPYRIMIDINES AS CYCLIN-DEPENDENT KINASE INHIBITORS
• the present invention relates to pyrazolo[1 ,5-a]pyrimidine compounds useful as protein kinase inhibitors (such as for example, the inhibitors of the cyclin-dependent kinases, mitogen-activated protein kinase (MAPK/ERK), glycogen synthase kinase 3(GSK3beta) and the like), pharmaceutical compositions containing the compounds, and methods of treatment using the compounds and compositions to treat diseases such as, for example, cancer, inflammation, arthritis, viral diseases, neurodegenerative diseases such as Alzheimer's disease, cardiovascular diseases, and fungal diseases.
• diseases such as, for example, cancer, inflammation, arthritis, viral diseases, neurodegenerative diseases such as Alzheimer's disease, cardiovascular diseases, and fungal diseases.
• Protein kinase inhibitors include kinases such as, for example, the inhibitors of the cyclin-dependent kinases (CDKs), mitogen activated protein kinase (MAPK/ERK), glycogen synthase kinase 3 (GSK3beta), and the like. Protein kinase inhibitors are described, for example, by M. Hale et al in WO02/22610 A1 and by Y. Mettey et al in J. Med. Chem., (2003) 46 222-236. The cyclin-dependent kinases are serine/threonine protein kinases, which are the driving force behind the cell cycle and cell proliferation.
• CDKs cyclin-dependent kinases
• MAPK/ERK mitogen activated protein kinase
• GSK3beta glycogen synthase kinase 3
• Protein kinase inhibitors are described, for example, by M. Hale et al in
• CDK1 , CDK2, CDK3, CDK4, CDK5, CDK6 and CDK7, CDK8 and the like perform distinct roles in cell cycle progression and can be classified as either G1 , S, or G2M phase enzymes.
• Uncontrolled proliferation is a hallmark of cancer cells, and misregulation of CDK function occurs with high frequency in many important solid tumors.
• CDK2 and CDK4 are of particular interest because their activities are frequently misregulated in a wide variety of human cancers.
• CDK2 activity is required for progression through G1 to the S phase of the cell cycle, and CDK2 is one of the key components of the G1 checkpoint.
• Checkpoints serve to maintain the proper sequence of cell cycle events and allow the cell to respond to insults or to proliferative signals, while the loss of proper checkpoint control in cancer cells contributes to tumorgenesis.
• the CDK2 pathway influences tumorgenesis at the level of tumor suppressor function (e.g. p52, RB, and p27) and oncogene activation (cyclin E).
• tumor suppressor function e.g. p52, RB, and p27
• cyclin E oncogene activation
• Both the coactivator, cyclin E, and the inhibitor, p27, of CDK2 are either over - or underexpressed, respectively, in breast, colon, nonsmall cell lung, gastric, prostate, bladder, non-Hodgkin's lymphoma, ovarian, and other cancers. Their altered expression has been shown to correlate with increased CDK2 activity levels and poor overall survival.
• CDK inhibitors are known.
• flavopiridol (Formula I) is a nonselective CDK inhibitor that is currently undergoing human clinical trials, A. M. Sanderowicz et al, J. Clin. Oncol. (1998) 16, 2986-2999.
• CDK inhibitors include, for example, olomoucine (J. Vesely et al, Eur. J. Biochem., (1994) 224, 771-786) and roscovitine (I. Meijer et al, Eur. J. Biochem., (1997) 243, 527-536).
• U.S. 6,107,305 describes certain pyrazolo[3,4-b] pyridine compounds as CDK inhibitors.
• An illustrative compound from the '305 patent has the Formula II:
• the present invention provides a novel class of pyrazolo[1 ,5-a]pyrimidine compounds as inhibitors of cyclin dependent kinases, methods of preparing such compounds, pharmaceutical compositions comprising one or more such compounds, methods of preparing pharmaceutical formulations comprising one or more such compounds, and methods of treatment, prevention, inhibition or amelioration of one or more diseases associated with the CDKs using such compounds or pharmaceutical compositions.
• the present application discloses a compound, or pharmaceutically acceptable salts or solvates of said compound, said compound having the general structure shown in Formula III:
• R is H, alkyl, alkenyl, alkynyl, arylalkyl, arylalkenyl, cycloalkyl, cycloalkylalkyl, alkenylalkyl, alkynylalkyl, heterocyclyl, heterocyclylalkyl, heteroarylalkyl (including N-oxide of said heteroaryl), -(CHR 5 ) n -aryl, -(CHR 5 ) n -
• each of said alkyl, alkenyl, alkynyl, aryl, cycloalkyl, heterocyclyl, and heteroaryl can be unsubstituted or optionally substituted with one or more moieties which can be the same or different, each moiety being independently selected from the group consisting of halogen, alkyl, aryl, cycloalkyl, heterocyclylalkyl, CF 3 , OCF 3 , CN, -OR 5 , -NR 5 R 10 , -C(R 4 R 5 ) P -R 9 , -N(R 5 )Boc, -(CR 4 R 5 ) p OR 5 , -C(O 2 )R 5 , -C(O)R 5 , -C(O)NR 5 R 10 , -SO 3 H, -SR 10 , -S(O 2 )R 7 , -S(O 2 )NR 5 R 10 , -N(R
• R 3 is selected from the group consisting of H, halogen, -NR 5 R 6 , -OR 6 , -SR 6 , -C(O)N(R 5 R 6 ), alkyl, alkynyl, cycloalkyl, aryl, arylalkyl, heterocyclyl, heterocyclylalkyl, heteroaryl and heteroarylalkyl,
• each of said alkyl, cycloalkyl, aryl, arylalkyl, heterocyclyl, heterocyclylalkyl, heteroaryl and heteroarylalkyl for R 3 and the heterocyclyl moieties whose structures are shown immediately above for R 3 can be unsubstituted or optionally independently substituted with one or more moieties which can be the same or different, each moiety being independently selected from the group consisting of halogen, alkyl, aryl, cycloalkyl, CF 3 , CN, -OCF 3 , -(CR 4 R 5 ) P OR 5 , -OR 5 , -NR 5 R 6 , -(CR 4 R 5 ) P NR 5 R 6 , -C(O 2 )R 5 , -C(O)R 5 , -C(O)NR 5 R 6 , -SR 6 , -S(O 2 )R 6 , -S(O 2 )NR 5 R
• R 9 is selected from the group consisting of halogen, -CN, -NR 5 R 10 , -C(O 2 )R 6 , -C(O)NR 5 R 10 , -OR 6 , -SR 6 , -S(O 2 )R 7 , -S(O 2 )NR 5 R 10 , -N(R 5 )S(O 2 )R 7 , -N(R 5 )C(O)R 7 and -N(R 5 )C(O)NR 5 R 10 ; m is 0 to 4; n is 1 to 4; and p is 1 to 4, with the proviso that when R 2 is phenyl, R 3 is not alkyl, alkynyl or halogen, and
• the compounds of Formula III can be useful as protein kinase inhibitors and can be useful in the treatment and prevention of proliferative diseases, for example, cancer, inflammation and arthritis. They may also be useful in the treatment of neurodegenerative diseases such Alzheimer's disease, cardiovascular diseases, viral diseases and fungal diseases.
• the present invention discloses pyrazolo[1 ,5- ajpyrimidine compounds which are represented by structural Formula III, or a pharmaceutically acceptable salt or solvate thereof, wherein the various moieties are as described above.
• R is -(CHR 5 ) n -aryl, -(CHR 5 ) n -heteroaryl, -(CHR 5 ) n -heteroaryl (with said heteroaryl being substituted with an additional, same or different, heteroaryl), -(CHR 5 ) n -heterocyclyl (with said heterocyclyl being substituted with an additional, same or different, heterocyclyl), or
• R 2 is halogen, CF 3 , CN, lower alkyl, alkyl substituted with -OR 6 , alkynyl, aryl, heteroaryl or heterocyclyl.
• R 3 is H, lower alkyl, aryl, heteroaryl, cycloalkyl,
• R 4 is H or lower alkyl.
• R 5 is H, lower alkyl or cycloalkyl.
• n 1 to 2.
• R is -(CHR 5 ) n -aryl, -(CHR 5 ) n -heteroaryl.
• R 2 is halogen, CF 3 , CN, lower alkyl, alkynyl, or alkyl substituted with -OR 6 .
• R 2 is lower alkyl, alkynyl or Br.
• R 3 is H, lower alkyl, aryl,
• alkyl, aryl and the heterocyclyl moieties shown immediately above for R 3 are optionally substituted with one or more moieties which can be the same or different, each moiety being independently selected from the group consisting of halogen, CF 3 , lower alkyl, hydroxyalkyl, alkoxy, -S(O 2 )R 5 , and CN.
• R 4 is H.
• R 5 is H, ethyl, cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl.
• R 8 is alkyl or hydroxyalkyl. In an additional embodiment, n is 1. In an additional embodiment, p is 1 or 2.
• Another embodiment discloses the inventive compounds shown in Table 1 , which exhibited CDK2 inhibitory activity of about 0.0001 ⁇ M to > about 5 ⁇ M.
• the assay methods are described later (from page 333 onwards).
• Another embodiment of the invention discloses the following compounds, which exhibited CDK2 inhibitory activity of about 0.0001 ⁇ M to about 0.5 ⁇ M: 24
• Another embodiment of the invention discloses the following compounds, which exhibited CDK2 inhibitory activity of about 0.0001 ⁇ M to about 0.1 ⁇ M: 28
• alkyl means an aliphatic hydrocarbon group which may be straight or branched and comprising about 1 to about 20 carbon atoms in the chain. Preferred alkyl groups contain about 1 to about 12 carbon atoms in the chain. More preferred alkyl groups contain about 1 to about 6 carbon atoms in the chain. Branched means that one or more lower alkyl groups such as methyl, ethyl or propyl, are attached to a linear alkyl chain.
• “Lower alkyl” means a group having about 1 to about 6 carbon atoms in the chain which may be straight or branched.
• substituted alkyl means that the alkyl group may be substituted by one or more substituents which may be the same or different, each substituent being independently selected from the group consisting of halo, alkyl, aryl, cycloalkyl, cyano, hydroxy, alkoxy, alkylthio, amino, -NH(alkyl), - NH(cycloalkyl), -N(alkyl) 2 , carboxy and -C(O)O-alkyl.
• suitable alkyl groups include methyl, ethyl, n-propyl, isopropyl and t-butyl.
• Alkynyl means an aliphatic hydrocarbon group containing at least one carbon-carbon triple bond and which may be straight or branched and comprising about 2 to about 15 carbon atoms in the chain.
• Preferred alkynyl groups have about 2 to about 12 carbon atoms in the chain; and more preferably about 2 to about 4 carbon atoms in the chain.
• Branched means that one or more lower alkyl groups such as methyl, ethyl or propyl, are attached to a linear alkynyl chain.
• “Lower alkynyl” means about 2 to about 6 carbon atoms in the chain which may be straight or branched.
• Non-limiting examples of suitable alkynyl groups include ethynyl, propynyl, 2-butynyl and 3-methylbutynyl.
• substituted alkynyl means that the alkynyl group may be substituted by one or more substituents which may be the same or different, each substituent being independently selected from the group consisting of alkyl, aryl and cycloalkyl.
• Aryl means an aromatic monocyclic or multicyclic ring system comprising about 6 to about 14 carbon atoms, preferably about 6 to about 10 carbon atoms.
• the aryl group can be optionally substituted with one or more "ring system substituents" which may be the same or different, and are as defined herein.
• suitable aryl groups include phenyl and naphthyl.
• Heteroaryl means an aromatic monocyclic or multicyclic ring system comprising about 5 to about 14 ring atoms, preferably about 5 to about 10 ring atoms, in which one or more of the ring atoms is an element other than carbon, for example nitrogen, oxygen or sulfur, alone or in combination. Preferred he teroaryls contain about 5 to about 6 ring atoms.
• the "heteroaryl” can be optionally substituted by one or more "ring system substituents" which may be the same or different, and are as defined herein.
• the prefix aza, oxa or thia before the heteroaryl root name means that at least a nitrogen, oxygen or sulfur atom respectively, is present as a ring atom.
• a nitrogen atom of a heteroaryl can be optionally oxidized to the corresponding N-oxide.
• suitable heteroaryls include pyridyl, pyrazinyl, furanyl, thienyl, pyrimidinyl, pyridone (including N-substituted pyridones), isoxazolyl, isothiazolyl, oxazolyl, thiazolyl, pyrazolyl, furazanyl, pyrrolyl, pyrazolyl, triazolyl, 1 ,2,4-thiadiazolyl, pyrazinyl, pyridazinyl, quinoxalinyl, phthalazinyl, oxindolyl, imidazo[1 ,2- ajpyridinyl, imidazo[2,1-b]thiazolyl, benzofurazanyl, indolyl, azaindolyl, benzimidazolyl,
• Aralkyl or “arylalkyl” means an aryl-alkyl- group in which the aryl and alkyl are as previously described. Preferred aralkyls comprise a lower alkyl group. Non-limiting examples of suitable aralkyl groups include benzyl, 2- phenethyl and naphthalenylmethyl. The bond to the parent moiety is through the alkyl.
• Alkylaryl means an alkyl-aryl- group in which the alkyl and aryl are as previously described. Preferred alkylaryls comprise a lower alkyl group. Non- limiting example of a suitable alkylaryl group is tolyl. The bond to the parent moiety is through the aryl.
• Cycloalkyl means a non-aromatic mono- or multicyclic ring system comprising about 3 to about 10 carbon atoms, preferably about 5 to about 10 carbon atoms. Preferred cycloalkyl rings contain about 5 to about 7 ring atoms. The cycloalkyl can be optionally substituted with one or more "ring system substituents" which may be the same or different, and are as defined above.
• Non-limiting examples of suitable monocyclic cycloalkyls include cyclopropyl, cyclopentyl, cyclohexyl, cycloheptyl and the like.
• Non-limiting examples of suitable multicyclic cycloalkyls include 1-decalinyl, norbornyl, adamantyl and the like, as well as partially saturated species such as, for example, indanyl, tetrahydronaphthyl and the like.
• Halogen means fluorine, chlorine, bromine, or iodine. Preferred are fluorine, chlorine and bromine.
• Ring system substituent means a substituent attached to an aromatic or non-aromatic ring system which, for example, replaces an available hydrogen on the ring system.
• Ring system substituents may be the same or different, each being independently selected from the group consisting of alkyl, alkenyl, alkynyl, aryl, heteroaryl, aralkyl, alkylaryl, heteroaralkyl, heteroarylalkenyl, heteroarylalkynyl, alkyl heteroaryl, hydroxy, hydroxyalkyl, alkoxy, aryloxy, aralkoxy, acyl, aroyl, halo, nitro, cyano, carboxy, alkoxycarbonyl, aryloxycarbonyl, aralkoxycarbonyl, alkylsulfonyl, arylsulfonyl, heteroarylsulfonyl, alkylthio, arylthio, heteroarylthio, aralkylthio, hetero
• Ring system substituent may also mean a single moiety which simultaneously replaces two available hydrogens on two adjacent carbon atoms (one H on each carbon) on a ring system.
• Examples of such moiety are methylene dioxy, ethylenedioxy, - C(CH 3 ) 2 - and the like which form moieties such as, for example:
• Heterocyclyl means a non-aromatic saturated monocyclic or multicyclic ring system comprising about 3 to about 10 ring atoms, preferably about 5 to about 10 ring atoms, in which one or more of the atoms in the ring system is an element other than carbon, for example nitrogen, oxygen or sulfur, alone or in combination. There are no adjacent oxygen and/or sulfur atoms present in the ring system.
• Preferred heterocyclyls contain about 5 to about 6 ring atoms.
• the prefix aza, oxa or thia before the heterocyclyl root name means that at least a nitrogen, oxygen or sulfur atom respectively is present as a ring atom.
• Any -NH in a heterocyclyl ring may exist protected such as, for example, as an -N(Boc), - N(CBz), -N(Tos) group and the like; such protections are also considered part of this invention.
• the heterocyclyl can be optionally substituted by one or more "ring system substituents" which may be the same or different, and are as defined herein.
• the nitrogen or sulfur atom of the heterocyclyl can be optionally oxidized to the corresponding N-oxide, S-oxide or S,S-dioxide.
• Non-limiting examples of suitable monocyclic heterocyclyl rings include piperidyl, pyrrolidinyl, piperazinyl, morpholinyl, thiomorpholinyl, thiazolidinyl, 1 ,4-dioxanyl, tetrahydrofuranyl, tetrahydrothiophenyl, lactam, lactone, and the like.
• hetero-atom containing ring systems of this invention there are no hydroxyl groups on carbon atoms adjacent to a N, O or S, as well as there are no N or S groups on carbon adjacent to another heteroatom.
• N, O or S there are no hydroxyl groups on carbon atoms adjacent to a N, O or S, as well as there are no N or S groups on carbon adjacent to another heteroatom.
• Alkynylalkyl means an alkynyl-alkyl- group in which the alkynyl and alkyl are as previously described. Preferred alkynylalkyls contain a lower alkynyl and a lower alkyl group. The bond to the parent moiety is through the alkyl. Non- limiting examples of suitable alkynylalkyl groups include propargylmethyl.
• Heteroaralkyl means a heteroaryl-alkyl- group in which the heteroaryl and alkyl are as previously described. Preferred heteroaralkyls contain a lower alkyl group.
• Non-limiting examples of suitable aralkyl groups include pyridylmethyl, and quinolin-3-ylmethyl. The bond to the parent moiety is through the alkyl.
• "Hydroxyalkyl” means a HO-alkyl- group in which alkyl is as previously defined. Preferred hydroxyalkyls contain lower alkyl.
• suitable hydroxyalkyl groups include hydroxymethyl and 2-hydroxyethyl.
• acyl means an H-C(O)-, alkyl-C(O)- or cycloalkyl-C(O)-, group in which the various groups are as previously described.
• the bond to the parent moiety is through the carbonyl.
• Preferred acyls contain a lower alkyl.
• suitable acyl groups include formyl, acetyl and propanoyl.
• Aroyl means an aryl-C(O)- group in which the aryl group is as previously described.
• the bond to the parent moiety is through the carbonyl.
• suitable groups include benzoyl and 1- naphthoyl.
• Alkoxy means an alkyl-O- group in which the alkyl group is as previously described.
• suitable alkoxy groups include methoxy, ethoxy, n-propoxy, isopropoxy and n-butoxy.
• the bond to the parent moiety is through the ether oxygen.
• Aryloxy means an aryl-O- group in which the aryl group is as previously described.
• suitable aryloxy groups include phenoxy and naphthoxy.
• the bond to the parent moiety is through the ether oxygen.
• Alkyloxy means an aralkyl-O- group in which the aralkyl group is as previously described.
• suitable aralkyloxy groups include benzyloxy and 1- or 2-naphthalenemethoxy.
• the bond to the parent moiety is through the ether oxygen.
• Alkylthio means an alkyl-S- group in which the alkyl group is as previously described.
• suitable alkylthio groups include methylthio and ethylthio. The bond to the parent moiety is through the sulfur.
• Arylthio means an aryl-S- group in which the aryl group is as previously described.
• suitable arylthio groups include phenylthio and naphthylthio.
• the bond to the parent moiety is through the sulfur.
• Alkylthio means an aralkyl-S- group in which the aralkyl group is as previously described. Non-limiting example of a suitable aralkylthio group is benzylthio. The bond to the parent moiety is through the sulfur.
• Alkoxycarbonyl means an alkyl-O-CO- group. Non-limiting examples of suitable alkoxycarbonyl groups include methoxycarbonyl and ethoxycarbonyl. The bond to the parent moiety is through the carbonyl.
• Aryloxycarbonyl means an aryl-O-C(O)- group.
• suitable aryloxycarbonyl groups include phenoxycarbonyl and naphthoxycarbonyl.
• the bond to the parent moiety is through the carbonyl.
• Alkoxycarbonyl means an aralkyl-O-C(O)- group.
• a suitable aralkoxycarbonyl group is benzyloxycarbonyl.
• the bond to the parent moiety is through the carbonyl.
• Alkylsulfonyl means an alkyl-S(O 2 )- group. Preferred groups are those in which the alkyl group is lower alkyl. The bond to the parent moiety is through the sulfonyl.
• Arylsulfonyl means an aryl-S(O 2 )- group. The bond to the parent moiety is through the sulfonyl.
• substituted means that one or more hydrogens on the designated atom is replaced with a selection from the indicated group, provided that the designated atom's normal valency under the existing circumstances is not exceeded, and that the substitution results in a stable compound. Combinations of substituents and/or variables are permissible only if such combinations result in stable compounds.
• stable compound' or “stable structure” is meant a compound that is sufficiently robust to survive isolation to a useful degree of purity from a reaction mixture, and formulation into an efficacious therapeutic agent.
• optionally substituted means optional substitution with the specified groups, radicals or moieties.
• isolated or “in isolated form” for a compound refers to the physical state of said compound after being isolated from a synthetic process or natural source or combination thereof.
• purified or “in purified form” for a compound refers to the physical state of said compound after being obtained from a purification process or processes described herein or well known to the skilled artisan, in sufficient purity to be characterizable by standard analytical techniques described herein or well known to the skilled artisan. It should also be noted that any heteroatom with unsatisfied valences in the text, schemes, examples and Tables herein is assumed to have the hydrogen atom(s) to satisfy the valences.
• protecting groups When a functional group in a compound is termed "protected", this means that the group is in modified form to preclude undesired side reactions at the protected site when the compound is subjected to a reaction. Suitable protecting groups will be recognized by those with ordinary skill in the art as well as by reference to standard textbooks such as, for example, T. W. Greene et al, Protective Groups in organic Synthesis (1991), Wiley, New York.
• variable e.g., aryl, heterocycle, R 2 , etc.
• its definition on each occurrence is independent of its definition at every other occurrence.
• composition is intended to encompass a product comprising the specified ingredients in the specified amounts, as well as any product which results, directly or indirectly, from combination of the specified ingredients in the specified amounts.
• Prodrugs and solvates of the compounds of the invention are also contemplated herein.
• the term "prodrug”, as employed herein, denotes a compound that is a drug precursor which, upon administration to a subject, undergoes chemical conversion by metabolic or chemical processes to yield a compound of Formula III or a salt and/or solvate thereof.
• a discussion of prodrugs is provided in T. Higuchi and V. Stella, Pro-drugs as Novel Delivery Systems (1987) 14 of the A.C.S. Symposium Series, and in Bioreversible Carriers in Drug Design, (1987) Edward B. Roche, ed., American Pharmaceutical Association and Pergamon Press, both of which are incorporated herein by reference thereto.
• Solvate means a physical association of a compound of this invention with one or more solvent molecules. This physical association involves varying degrees of ionic and covalent bonding, including hydrogen bonding. In certain instances the solvate will be capable of isolation, for example when one or more solvent molecules are incorporated in the crystal lattice of the crystalline solid.
• Solvate encompasses both solution-phase and isolatable solvates. Non-limiting examples of suitable solvates include ethanolates, methanolates, and the like.
• “Hydrate” is a solvate wherein the solvent molecule is H 2 O.
• Effective amount or “therapeutically effective amount” is meant to describe an amount of compound or a composition of the present invention effective in inhibiting the CDK(s) and thus producing the desired therapeutic, ameliorative, inhibitory or preventative effect.
• the compounds of Formula III can form salts which are also within the scope of this invention.
• Reference to a compound of Formula III herein is understood to include reference to salts thereof, unless otherwise indicated.
• the term "salt(s)" denotes acidic salts formed with inorganic and/or organic acids, as well as basic salts formed with inorganic and/or organic bases.
• zwitter ions when a compound of Formula III contains both a basic moiety, such as, but not limited to a pyridine or imidazole, and an acidic moiety, such as, but not limited to a carboxylic acid, zwitter ions (“inner salts”) may be formed and are included within the term "salt(s)" as used herein.
• Salts of the compounds of the Formula III may be formed, for example, by reacting a compound of Formula III with an amount of acid or base, such as an equivalent amount, in a medium such as one in which the salt precipitates or in an aqueous medium followed by lyophilization.
• Exemplary acid addition salts include acetates, ascorbates, benzoates, benzenesulfonates, bisulfates, borates, butyrates, citrates, camphorates, camphorsulfonates, fumarates, hydrochlorides, hydrobromides, hydroiodides, lactates, maleates, methanesulfonates, naphthalenesulfonates, nitrates, oxalates, phosphates, propionates, salicylates, succinates, sulfates, tartarates, thiocyanates, toluenesulfonates (also known as tosylates,) and the like.
• Exemplary basic salts include ammonium salts, alkali metal salts such as sodium, lithium, and potassium salts, alkaline earth metal salts such as calcium and magnesium salts, salts with organic bases (for example, organic amines) such as dicyclohexylamines, t-butyl amines, and salts with amino acids such as arginine, lysine and the like.
• Basic nitrogen-containing groups may be quarternized with agents such as lower alkyl halides (e.g. methyl, ethyl, and butyl chlorides, bromides and iodides), dialkyl sulfates (e.g.
• dimethyl, diethyl, and dibutyl sulfates dimethyl, diethyl, and dibutyl sulfates
• long chain halides e.g. decyl, lauryl, and stearyl chlorides, bromides and iodides
• aralkyl halides e.g. benzyl and phenethyl bromides
• All stereoisomers for example, geometric isomers, optical isomers and the like
• of the present compounds including those of the salts, solvates and prodrugs of the compounds as well as the salts and solvates of the prodrugs
• those which may exist due to asymmetric carbons on various substituents including enantiomeric forms (which may exist even in the absence of asymmetric carbons), rotameric forms, atropisomers, and diastereomeric forms, are contemplated within the scope of this invention, as are positional isomers (such as, for example, 4-pyridyl and 3-pyridyl).
• Individual stereoisomers of the compounds of the invention may, for example, be substantially free of other isomers, or may be admixed, for example, as racemates or with all other, or other selected, stereoisomers.
• the chiral centers of the present invention can have the S or R configuration as defined by the IUPAC 1974 Recommendations.
• the use of the terms "salt”, “solvate” "prodrug” and the like, is intended to equally apply to the salt, solvate and prodrug of enantiomers, stereoisomers, rotamers, tautomers, positional isomers, racemates or prodrugs of the inventive compounds.
• the compounds according to the invention have pharmacological properties; in particular, the compounds of Formula III can be inhibitors of protein kinases such as, for example, the inhibitors of the cyclin-dependent kinases, mitogen-activated protein kinase (MAPK/ERK), glycogen synthase kinase 3(GSK3beta) and the like.
• the cyclin dependent kinases (CDKs) include, for example, CDC2 (CDK1 ), CDK2, CDK4, CDK5, CDK6, CDK7 and CDK8.
• novel compounds of Formula III are expected to be useful in the therapy of proliferative diseases such as cancer, autoimmune diseases, viral diseases, fungal diseases, neurological/ neurodegenera tive disorders, arthritis, inflammation, anti-proliferative (e.g., ocular retinopathy), neuronal, alopecia and cardiovascular disease.
• proliferative diseases such as cancer, autoimmune diseases, viral diseases, fungal diseases, neurological/ neurodegenera tive disorders, arthritis, inflammation, anti-proliferative (e.g., ocular retinopathy), neuronal, alopecia and cardiovascular disease.
• proliferative diseases such as cancer, autoimmune diseases, viral diseases, fungal diseases, neurological/ neurodegenera tive disorders, arthritis, inflammation, anti-proliferative (e.g., ocular retinopathy), neuronal, alopecia and cardiovascular disease.
• anti-proliferative e.g., ocular retinopathy
• neuronal e.g., alopecia and cardiovascular
• the compounds of Formula III can be useful in the treatment of a variety of cancers, including (but not limited to) the following: carcinoma, including that of the bladder, breast, colon, kidney, liver, lung, including small cell lung cancer, esophagus, gall bladder, ovary, pancreas, stomach, cervix, thyroid, prostate, and skin, including squamous cell carcinoma; hematopoietic tumors of lymphoid lineage, including leukemia, acute lymphocytic leukemia, acute lymphoblastic leukemia, B-cell lymphoma, T- cell lymphoma, Hodgkins lymphoma, non-Hodgkins lymphoma, hairy cell lymphoma and Burkett's lymphoma; hematopoietic tumors of myeloid lineage, including acute and chronic myelogenous leukemias, myelodysplastic syndrome and promyelocytic leukemia; tumors of mesenchymal origin, including fibrosar
• inhibitors could act as reversible cytostatic agents which may be useful in the treatment of any disease process which features abnormal cellular proliferation, e.g., benign prostate hyperplasia, familial adenomatosis polyposis, neuro-fibromatosis, atherosclerosis, pulmonary fibrosis, arthritis, psoriasis, glomerulonephritis, restenosis following angioplasty or vascular surgery, hypertrophic scar formation, inflammatory bowel disease, transplantation rejection, endotoxic shock, and fungal infections.
• any disease process e.g., benign prostate hyperplasia, familial adenomatosis polyposis, neuro-fibromatosis, atherosclerosis, pulmonary fibrosis, arthritis, psoriasis, glomerulonephritis, restenosis following angioplasty or vascular surgery, hypertrophic scar formation, inflammatory bowel disease, transplantation rejection, endotoxic shock, and fungal infections.
• Compounds of Formula III may also be useful in the treatment of Alzheimer's disease, as suggested by the recent finding that CDK5 is involved in the phosphorylation of tau protein (J. Biochem, (1995) 117. 741-749).
• Compounds of Formula III may induce or inhibit apoptosis.
• the apoptotic response is aberrant in a variety of human diseases.
• Compounds of Formula III, as modulators of apoptosis, will be useful in the treatment of cancer (including but not limited to those types mentioned hereinabove), viral infections (including but not limited to herpevirus, poxvirus, Epstein- Barr virus, Sindbis virus and adenovirus), prevention of AIDS development in HIV-infected individuals, autoimmune diseases (including but not limited to systemic lupus, erythematosus, autoimmune mediated glomerulonephritis, rheumatoid arthritis, psoriasis, inflammatory bowel disease, and autoimmune diabetes mellitus), neurodegenerative disorders (including but not limited to Alzheimer's disease, AIDS-related dementia, Parkinson's disease, amyotrophic lateral sclerosis, retinitis pigmentosa, spinal muscular atrophy and cerebellar degeneration), mye
• Compounds of Formula III can modulate the level of cellular RNA and DNA synthesis. These agents would therefore be useful in the treatment of viral infections (including but not limited to HIV, human papilloma virus, herpesvirus, poxvirus, Epstein-Barr virus, Sindbis virus and adenovirus).
• viral infections including but not limited to HIV, human papilloma virus, herpesvirus, poxvirus, Epstein-Barr virus, Sindbis virus and adenovirus.
• Chemoprevention is defined as inhibiting the development of invasive cancer by either blocking the initiating mutagenic event or by blocking the progression of pre-malignant cells that have already suffered an insult or inhibiting tumor relapse.
• Compounds of Formula III may also be useful in inhibiting tumor angiogenesis and metastasis.
• Compounds of Formula III may also act as inhibitors of other protein kinases, e.g., protein kinase C, her2, raf 1 , MEK1 , MAP kinase, EGF receptor, PDGF receptor, IGF receptor, PI3 kinase, weel kinase, Src, Abl and thus be effective in the treatment of diseases associated with other protein kinases.
• protein kinase C her2, raf 1 , MEK1
• MAP kinase e.g., EGF receptor, PDGF receptor, IGF receptor, PI3 kinase, weel kinase, Src, Abl
• Another aspect of this invention is a method of treating a mammal (e.g., human) having a disease or condition associated with the CDKs by administering a therapeutically effective amount of at least one compound of Formula III, or a pharmaceutically acceptable salt or solvate of said compound to the mammal.
• a mammal e.g., human
• a preferred dosage is about 0.001 to 500 mg/kg of body weight/day of the compound of Formula III.
• An especially preferred dosage is about 0.01 to 25 mg/kg of body weight/day of a compound of Formula III, or a pharmaceutically acceptable salt or solvate of said compound.
• the compounds of this invention may also be useful in combination (administered together or sequentially) with one or more of anti-cancer treatments such as radiation therapy, and/or one or more anti-cancer agents selected from the group consisting of cytostatic agents, cytotoxic agents (such as for example, but not limited to, DNA interactive agents (such as cisplatin or doxorubicin)); taxanes (e.g.
• topoisomerase II inhibitors such as etoposide
• topoisomerase I inhibitors such as irinotecan (or CPT-11 ), camptostar, or topotecan
• tubulin interacting agents such as paclitaxel, docetaxel or the epothilones
• hormonal agents such as tamoxifen
• thymidilate synthase inhibitors such as 5-fluorouracil
• anti-metabolites such as methoxtrexate
• alkylating agents such as temozolomide (TEMODARTM from Schering-Plough Corporation, Kenilworth, New Jersey), cyclophosphamide
• Farnesyl protein transferase inhibitors such as, SARASARTM(4-[2-[4-[(11 R)- 3,10-dibromo-8-chloro-6,11-dihydro-5H-benzo[5,6]cyclohepta[1 ,2-b
• anti-cancer agents include but are not limited to Uracil mustard, Chlormethine, Ifosfamide, Melphalan, Chlorambucil, Pipobroman, Triethylenemelamine, Triethylenethiophosphoramine, Busulfan, Carmustine, Lomustine, Streptozocin, dacarbazine, Floxuridine, Cytarabine, 6-Mercaptopurine, 6-Thioguanine, Fludarabine phosphate, oxaliplatin, leucovirin, oxaliplatin (ELOXATINTM from Sanofi-Synthelabo Pharmaeuticals, France), Pentostatine, Vinblastine, Vincristine, Vindesine, Bleomycin, Dactinomycin, Daunorubicin, Doxorubicin, Epirubicin, Idarubicin, Mithramycin, Deoxycoformycin, Mitomycin-C, L-Asparaginase, Teniposide
• Aminoglutethimide Estramustine, Medroxyprogesteroneacetate, Leuprolide, Flutamide, Toremifene, goserelin, Cisplatin, Carboplatin, Hydroxyurea, Amsacrine, Procarbazine, Mitotane, Mitoxantrone, Levamisole, Navelbene, Anastrazole, Letrazole, Capecitabine, Reloxaf ⁇ ne, Droloxafine, or Hexamethylmelamine.
• such combination products employ the compounds of this invention within the dosage range described herein and the other pharmaceutically active agent or treatment within its dosage range.
• the CDC2 inhibitor olomucine has been found to act synergistically with known cytotoxic agents in inducing apoptosis (J. Cell Sci., (1995) 108, 2897.
• Compounds of Formula III may also be administered sequentially with known anticancer or cytotoxic agents when a combination formulation is inappropriate.
• the invention is not limited in the sequence of administration; compounds of Formula III may be administered either prior to or after administration of the known anticancer or cytotoxic agent.
• this invention includes combinations comprising an amount of at least one compound of Formula III, or a pharmaceutically acceptable salt or solvate thereof, and an amount of one or more anti-cancer treatments and anti-cancer agents listed above wherein the amounts of the compounds/ treatments result in desired therapeutic effect.
• the pharmacological properties of the compounds of this invention may be confirmed by a number of pharmacological assays.
• the exemplified pharmacological assays which are described later have been carried out with the compounds according to the invention and their salts.
• compositions which comprise at least one compound of Formula III, or a pharmaceutically acceptable salt or solvate of said compound and at least one pharmaceutically acceptable carrier.
• inert, pharmaceutically acceptable carriers can be either solid or liquid.
• Solid form preparations include powders, tablets, dispersible granules, capsules, cachets and suppositories.
• the powders and tablets may be comprised of from about 5 to about 95 percent active ingredient.
• Suitable solid carriers are known in the art, e.g., magnesium carbonate, magnesium stearate, talc, sugar or lactose. Tablets, powders, cachets and capsules can be used as solid dosage forms suitable for oral administration. Examples of pharmaceutically acceptable carriers and methods of manufacture for various compositions may be found in A. Gennaro (ed.), Remington's
• Liquid form preparations include solutions, suspensions and emulsions. As an example may be mentioned water or water-propylene glycol solutions for parenteral injection or addition of sweeteners and opacifiers for oral solutions, suspensions and emulsions. Liquid form preparations may also include solutions for intranasal administration.
• Aerosol preparations suitable for inhalation may include solutions and solids in powder form, which may be in combination with a pharmaceutically acceptable carrier, such as an inert compressed gas, e.g. nitrogen.
• a pharmaceutically acceptable carrier such as an inert compressed gas, e.g. nitrogen.
• solid form preparations that are intended to be converted, shortly before use, to liquid form preparations for either oral or parenteral administration.
• liquid forms include solutions, suspensions and emulsions.
• the compounds of the invention may also be deliverable transdermally.
• the transdermal compositions can take the form of creams, lotions, aerosols and/or emulsions and can be included in a transdermal patch of the matrix or reservoir type as are conventional in the art for this purpose.
• the compounds of this invention may also be delivered subcutaneously.
• the compound is administered orally.
• the pharmaceutical preparation is in a unit dosage form.
• the preparation is subdivided into suitably sized unit doses containing appropriate quantities of the active component, e.g., an effective amount to achieve the desired purpose.
• the quantity of active compound in a unit dose of preparation may be varied or adjusted from about 1 mg to about 100 mg, preferably from about 1 mg to about 50 mg, more preferably from about 1 mg to about 25 mg, according to the particular application.
• the actual dosage employed may be varied depending upon the requirements of the patient and the severity of the condition being treated. Determination of the proper dosage regimen for a particular situation is within the skill of the art. For convenience, the total daily dosage may be divided and administered in portions during the day as required.
• a typical recommended daily dosage regimen for oral administration can range from about 1 mg/day to about 500 mg/day, preferably 1 mg/day to 200 mg/day, in two to four divided doses.
• kits comprising a therapeutically effective amount of at least one compound of Formula III, or a pharmaceutically acceptable salt or solvate of said compound and a pharmaceutically acceptable carrier, vehicle or diluent.
• a kit comprising an amount of at least one compound of Formula III, or a pharmaceutically acceptable salt or solvate of said compound and an amount of at least one anticancer therapy and/or anti-cancer agent listed above, wherein the amounts of the two or more ingredients result in desired therapeutic effect.
• VXR-200 (200 MHz, 1 H), Varian Gemini-300 (300 MHz) or XL-400 (400
• the chlorides of type 9 can be prepared by treatment of the pyridones 8 with POCI 3 .
• R 2 is equal to H, substitution in this position is possible on the compounds of type 9 by electrophilic halogenation, acylation, and various other electrophilic aromatic substitutions.
• the chlorides of type 14 can be prepared by treatment of the pyridones 13 with POCI 3 .
• R 2 is H
• substitution in this position is possible on compounds of type 9 by electrophilic halogenation, acylation, and various other electrophilic aromatic substitutions.
• Incorporation of the N7-amino functionality can be accomplished through regioselective displacement of the chloride of compounds of type 14. Incorporation of the N5-amino functionality by addition of an appropriate amine at higher temperature.
• the chlorides of type 14 can be prepared by treatment of the pyridones 13 with POCI 3 .
• R 2 is equal to H, substitution in this position is possible on compounds of type 14 by electrophilic halogenation, acylation, and various other electrophilic aromatic substitutions.
• Incorporation of the N7-amino functionality can be accomplished through displacement of the chloride of compounds of type 15.
• BH 3 -THF solution (1 M, 24 mL, 5 eq) was added slowly to a stirring solution of 4-(2-pyridyl)-benzonitrile ( 0.85 g, 4.72 mmol ) in anhydrous THF ( 25 mL ) under Ar, and the resulting solution was refluxed for about 12 hr. The solution was cooled to 0°C using ice-water. Methanol (15 mL) was added drop- wise to the cold reaction mixture and stirred for 1 h to destroy excess BH 3 . Added HCl - methanol (1M, 10 mL) slowly to the reaction mixture and refluxed for 5 h.
• 3(R/S)-(fett-Butoxycarbonylaminomethyl)piperidine (3g, 14.0mmoles) was dissolved in anhydrous dichloromethane (50mL) and trimethylsilylisocyanate (9.68g. 11.4mL, 84.0mmoles) was added. The mixture was stirred under argon at 25°C for 68h. Additional trimethylsilylisocyanate (4.84g, 5.7mL, 42.0mmoles) was added and the mixture was stirred at 25°C for a total of 90h.
• 3-(2-ferf-Butoxycarbonylaminoethyl)piperidine (500mg, 2.19mmoles) was dissolved in anhydrous dichloromethane (10mL) and trimethylsilylisocyanate (2.96mL, 21.9mmoles) was added. The mixture was stirred under argon at 25°C for 3.35h. The mixture was diluted with dichloromethane and washed with saturated aqueous sodium bicarbonate.
• 3-(2-te/ ⁇ -Butoxycarbonylaminoethyl)piperidine-1-carboxamide (392.7mg, 1.45mmoles) (prepared as described in Preparative Example 242, Step A above) was dissolved in methanol (7.5mL) and 10% cone, sulfuric acid in 1 ,4-dioxane (19.5mL) was added. The mixture was stirred at 25°C for 1.25h. The mixture was diluted with methanol and BioRad AG1-X8 resin (OH " form) was added until the pH was basic.
• Isonipecotamide (10g, 78.0mmoles) was dissolved in distilled water (100mL) and 37% aqueous formaldehyde (7.6mL, equivalent to 2.81 g HCHO, 93.6mmoles) was added.
• Wet 10% Pd-C (8 spoon spatulas) was added under argon and the mixture was hydrogenated at 25°C and 50psi for 43h.
• the catalyst was filtered off through Celite and the latter was washed with water and methanol.
• 1-Methylisonipecotamide (6.75g, 47.5mmoles) (prepared as described in Preparative Example 245, Step A above) was dissolved in anhydrous THF (350mL) and the resulting mixture was added in portions to a stirred slurry of lithium aluminum hydride (1.8g, 47.5mmoles) in anhydrous THF (100mL) at 0°C under nitrogen. The mixture was stirred at 0°C for 30min and then heated at 66°C for 25h under nitrogen.
• Step A (0.68 g, 3.0 mmol) in THF (20 mL) at 0 °C was added MeMgl (5.1 mL, 3.0M in E. 2 O) dropwise over 10 min.
• the resulting solution was stirred for 16 h at rt whereupon the mixture was quenched by addition of sat. aq. NH CI.
• the mixture was concentrated to dryness and the resultant residue was stirred with EtOAc (100 mL) for 45 min and filtered. The filtrate was concentrated under reduced pressure to afford 0.68g (100%) of a yellow/orange oil.
• M+H 226.
• the crude material was taken onto Step C without further purification.
• the aldehyde was prepared according to the procedure of Gupton (J. Heterocyclic Chem. (1991 ), 28, 1281 ). PREPARATIVE EXAMPLE 255
• Example 28 1 H NMR (CDC l 3 ) ⁇ 8.86 (s, 1H), 8.74 (m, 1H), 8.17 (s, 1H), 7.97
• Example 46 1 H NMR (CDCI 3 ) ⁇ 8.79(s, 1H), 8.72(d, 1H), 8.14(s, 1H), 7.84(d,
• Example 110 1 H NMR (CDCI 3 ) ⁇ 8.18(t, 1H), 8.03(s, 1H), 7.44(m, 1H), 7.30(t,
• Example 112 1 H NMR (CDCI 3 ) ⁇ 8.22(t, 1H), 8.15(s, 1H), 7.51-7.33(m, 7H),
• Example 116 1 H NMR (CDCI 3 ) ⁇ 8.67(s, 1H), 8.55(d, 1H), 8.50(s, 1H), 7.92(d, 1H), 7.90(d, 1H), 7.78(t, 1H), 7.10(d, 1H), 6.97(s, 1H), 5.11(s, 2H), 3.77(s, 6H)
• Example 117 1 H NMR (CDCI 3 ) ⁇ 8.38(s, 1H), 8.30(d, 1H), 8.17(s, 1H), 7.52- 7.37(m, 6H), 6.97(t, 1H), 6.13(s, 1H), 4.77(d, 2H), 2.50(s, 3H)
• Example 118 1 H NMR (CDCI 3 ) ⁇ 8.18(t, 1H), 8.03(s, 1H), 7.44(m, 1H), 7.30(t, 1H), 7.17(q, 1H), 6.66(s, 1H), 6.56(br, 1H), 4.
• Example 126 1 H NMR (CDCI 3 ) ⁇ 8.15 (dt, 1H), 8.0 (s, 1H), 7.5 (d, 1H), 7.42 - 7.35 ( m, 2H), 7.3-7.2 (m, 2H), 7.15 (dd, 1H), 7.1 (dd, 1H), 7.0 (t, 1H), 6.6 (s, 1H),4.8(d,2H).
• Example 127 1 H NMR (CDCI 3 ) ⁇ 8.2 (dt, 1H), 8.0 (s,1H), 7.4 (dd, 1H), 7.3- 7.25 (m, 3H), 7.1 (dd, 1H), 6.9 - 6.85 (m, 2H), 6.7 (t, 1H), 6.6 (s, 1H), 4.6 (d, 2H), 3.2 (m, 4H), 2.6 (m, 4H), 2.3 (s, 3H)
• Example 128 1 H NMR (CDCI 3 ) ⁇ 8.15 (dt,1H), 8.1 (s, 1H), 8.0 (d, 2H), 7.5 (d, 2H), 7.4 (m, 2H), 7.25 (d, 1H), 7.2 (s,1H), 7.15 (dd, 1H), 7.0 (s, 1H), 6.8 (t, 1H), 6.6 (s, 1H),4.75(d,2H).
• Example 129 1 H NMR (CDCI 3 ) ⁇ 8.15 (dt, 1H), 8.05 (s, 1H), 8.0 (d, 2H), 7.5 (d, 2H), 7.4 (m, 1H), 7.3 (dd, 1H), 7.15 (dd, 1H), 6.9 (t, 1H), 6.5 (s, 1H), 4.75 (d, 2H), 3.85 (s, 3H)
• Example 130 1 H NMR (CDCI 3 ) ⁇ 8.2 (dt,1H), 8.0 (s, 1H), 7.4 (dd, 1H), 7.3(dd, 1H), 7.15 (dd, 1H), 6.8 (t, 1H), 6.4 (s,1H), 4.2 (d, 2H), 3.8 (s, 3H).
• Example 131 1 H NMR (CDCI 3 ) ⁇ 8.2 (dt, 1H), 8.0 (s,1H), 7.4 - 7.15 (m, 3H), 6.7 (t, 1 H), 4.2 (q, 2H), 3.8 (dt, 2H), 2.8 (t, 2H), 1.2 (t, 3H)
• Example 132 1 H NMR (CDCI 3 ) ⁇ 8.2 (dt, 1H), 8.0 (s,1H), 7.4 - 7.15 (m, 3H), 6.7 (t, 1H), 4.2 (q, 2H), 3.8 (dt, 2H), 2.8 (t, 2H), 2.05 (m, 2H) 1.2 (t, 3H)
• Example 133 1 H NMR (CDCI 3 ) ⁇ 8.15 (dt, 1H), 8.0 (s,1H), 7.4 (m, 1H), 7.3 (dd 1 H), 7.2 (dd, 1 H), 6.5 (s, 1 H), 6.4 (t,1 H
• Example 134 1 H NMR (CDCI 3 ) ⁇ 8.15 (dt, 1H), 8.0 (s, 1H), 7.95 (d, 2H), 7.6 (d, 2H), 7.4 (m, 1H), 7.25 (dd, 1H), 7.1 (dd, 1H), 6.9 (t, 1H), 6.5 (s, 1H), 4.8 (d, 2H), 3.0 (s, 3H)
• Example 135 1 H NMR (DMSO d6) ⁇ 9.1 (bs, 2H), 8.4 (s,1 H), 8.0 (t, 1 H), 7.85 (d, 2H), 7.7 (d, 2H), 7.6 (m, 1H), 7.4 (m, 2H), 6.6 (s, 1H), 4.8 (bs, 2H)
• Example 136 1 H NMR (CDCI 3 ) ⁇ 8.2 (dt, 1H), 8.0 (s,1H), 7.4 (m, 1H), 7.25 (dd, 1H), 7.15 (dd, 1H), 6.9 (m, 3H), 6.7 (t, 1H), 6.5 (s, 1H), 4.5 (d, 2H), 4.2 (s, 4H)
• Example 137 1 H NMR (CDCI 3 ) ⁇ 8.2 (dt, 1H), 8.0 (s, 1H), 7.4 (m, 1H), 7.3 (dd, 1H), 7.2 (dd, 1H), 6.9 (dd, 1H), 6.8 (t, 1H), 6.7 (m, 1H), 6.6 (s, 1H), 5.3 (s, 2H), 4.85 (s, 2H), 4.6 (d, 2H).
• Example 138 1 H NMR (CDCI 3 ) ⁇ 8.2 (dt, 1 H), 8.0 (s, 1 H), 7.9 (d,1 H), 7.8 (d, 1 H), 7.4 (m, 2H), 7.3 (dd, 1H), 7.1 (dd, 1H), 6.9 (t, 1H), 6.6 (s, 1H), 4.8 (d, 2H)
• Example 139 1 H NMR (CDCI 3 ) ⁇ 8.2 (dt, 1H), 8.0 (s, 1H), 7.4 (m, 1H), 7.3 (m, 2H), 7.2 (dd, 1H), 7.1 (dd, 1H), 6.8 (d, 1H), 6.7 (t, 1H), 6.6(s, 1H), 4.6 (m, 4H), 3.2 (t, 2H)
• Example 140 1 H NMR (CDCI 3 ) ⁇ 8.45 (s, 1H), 8.2 (dt, 1H), 8.0 (s, 1H), 7.7 (dd, 1 H), 7.4 - 7.3 (m, 3H), 7.15 (dd, 1 H), 6.8 (t, 1 H), 6.6 (s,1 H), 4.7 (d, 2H)
• Example 141 1 H NMR (CDCI 3 ) ⁇ 8.2 (dt, 1H), 8.0 (s, 1H), 7.45 - 7.1 (m, 7H), 6.6 (s, 1H), 4.4 (dt, 2H), 2.6 (t, 2H), 1.8 (m, 2H), 1.4 (m, 2H)
• Example 173 1 H NMR (DMSO-d 6 ) ⁇ 8.86 (s, 1H), 8.46 (s, 1H), 8.32-8.28 (m,
• Example 181 1 H NMR (300MHz, CDCI 3 ) D 8.41 (s, 1H), 8.28 - 8.23 (d, 1H),
• Example 184 1 H NMR (300MHz, CDCI 3 ) DD8.96 - 8.90 (s, 1H), 8.08 (s, 1H), 8.04 (d, 1 H), 7.72 (d, 1 H), 7.70 - 7.61 (dd, 1 H), 7.24 - 7.20 (dd, 1 H), 6.92 - 6.84
• Example 186 1 H NMR (300MHz, CDCI 3 ) D D8.96 - 8.90 (s, 1 H), 8.08 (s, 1 H),
• Example 196 1 H NMR (CD 3 OD) ⁇ 8.73(d, 1H), 8.58(q, 1H), 8.12(s, 1H), 8.00(d,
• Example 197 1 H NMR (CD 3 OD) ⁇ 8.73(d, 1 H), 8.58(q, 1 H), 8.12(s, 1 H), 8.00(d, 1 H), 7.54(q, 1 H), 6.19(s, 1 H), 4.86(s, 2H), 4.22-4.08(m, 2H), 4.03-3.93(m, 2H), 3.63(m, 1 H), 2.50-2.39(m, 1H), 2.32-2.21 (m, 1 H).
• Example 199 1 H NMR (300MHz, CDCI 3 ) DD8.29 (s, 1H), 8.15 (br s, 1 H), 7.95 (s, 1 H), 7.28 (d, 1 H), 7.05 - 6.95 (appt t, 1 H), 5.70 (s, 1 H), 4.62 (d, 2H), 2.90 (m, 1 H), 2.30 (m, 1 H), 1.9 - 1.2 (m, 8H), 0.65 (d, 3H).
• Example 200 1 H NMR (300MHz, CDCI 3 ) DD 8.71 (s, 2H), 8.00 (s, 1H), 6.13 (s, 1 H), 3.59 (s, 2H), 3.01 - 2.58 (m, 1 H), 2.51 - 2.45 (m, 1 H), 2.44 -2.30 (m,1 H), 2.20 (s, 3H), 2.09 - 1.95 (m, 2H), 1.85 -1.70 (m, 2H), 0.80 - 0.76 (d, 3H).
• Example 203 1 H NMR (300MHz, CDCI 3 ) D D8.10 (s, 1H), 8.08 (s, 1H), 6.27 (s, 2H), 4.95 (s, 2H), 3.00 - 2.90 (dd, 2H), 2.60 (m, 2H), 2.48 (br s, 1 H), 2.39 (s, 3h), 2.25 m, 1 H), 1.95 - 1.70 (m, 3H).
• Example 213 By essentially the same procedure set forth in Example 213 combining the compounds shown in Column 2 of Table 19 with compounds in Column 3 of Table 19, the compounds shown in Column 3 of Table 19 were prepared.
• Example 218 By essentially the same procedure set forth in Example 218 combining the compounds shown in Column 1 of Table 20 with the appropriate alcohol , the compounds shown in Column 2 of Table 20 were prepared.
• Example 227 By essentially the same procedure set forth in Example 227 combining the compounds shown in Column 1 of Table 21 with the appropriate amine, the compounds shown in Column 2 of Table 21 were prepared.
• Example 236 By essentially the same procedure set forth in Example 236 combining the compounds shown in Column 2 and 3 of Table 22, the compounds shown in Column 4 of Table 22 were prepared.
• Example 262 By essentially the same procedure set forth in Example 262 starting from the compounds shown in Column 1 of Table 24, the compounds shown in Column 2 of Table 24 were prepared.
• Step D By essentially the same procedure set forth in Preparative Example 200 only substituting the compound prepared in Example 276, Step B, the above compound was prepared (0.1g, 100% yield). Step D:
• the palladium-catalyzed zinc cross-coupling reaction was carried out in a manner similar to the procedure described in J. Org. Chem. (1999), 453.
• a solution of the chloropyrazolopyrimidine (200 mg, 0.458 mmol), Pd(PPh 3 ) 4 (53 mg, 0.046 mmol), and exo-2-norbonylzinc bromide (0.5 M in THF, 0.95 mL, 0.47 mmol) in DMF (2 mL) was refluxed at 100°C (oil bath temp.) overnight.
• the reaction mixture was quenched with half-saturated NH 4 CI and extracted with CH 2 CI 2 .
• the organic phase was dried over MgSO 4 and concentrated under reduced pressure.
• Example 304 By essentially the same procedure set forth in Example 304, utilizing the aldehyde from Example 303 and substituting the Grignard or organolithium reagents shown in Column 2 of Table 28, the compounds in Column 3 of Table 28 were prepared:
• Step B (41 mg, 0.078 mmol) in CH 2 CI 2 (2 mL) was added MCPBA (33 mg, 0.19 mmol) in one portion.
• the resulting mixture was stirred for 3h at rt and the mixture was diluted with CH 2 CI 2 (5 mL) and sat. aq. NaHCO 3 (2.5 mL).
• the layers were separated, the aqueous layer was extracted with CH 2 CI 2 (2 x 5 mL), and the organic layers were combined.
• the organic layer was dried (Na 2 SO 4 ), filtered, and concentrated under reduced pressure to afford 40 mg (92%) of the sulfone adduct as a light yellow solid.
• M+H 560.
• Step A To a solution of the compound prepared in Example 340, Step A (135 mg, 0.28 mmol) in CH 2 CI 2 (2 mL) at rt was added TFA (0.54 mL, 7.0 mmol) dropwise. The resulting solution was stirred for 18 h at rt and was concentrated under reduced pressure. The crude material was redissolved in CH 2 CI 2 (5 mL) and the organic layer was sequentially washed with sat. aq. NaHCO 3 (2 x 2 mL) and brine (1 x 2 mL). The organic layer was dried (Na 2 SO 4 ), filtered, and concentrated under reduced pressure.
• Step A To a mixture of the compound prepared in Example 341 , Step A (0.14 g, 0.26 mmol) in EtOH : H 2 O (3 mL, 2 : 1) was added KOH (0.29 g, 20 eq.) in one portion. The resulting solution was stirred at reflux 14 hours, cooled to room temperature, and concentrated under reduced pressure. The residue was taken up in CH 2 CI 2 (5 mL) and diluted with saturated NaHCO 3 (2 mL). The layers were separated and the aqueous layer extracted with CH 2 CI2 (2 x 4 mL). The combined organics were washed with brine, dried over Na 2 SO 4 , filtered, and concentrated under reduced pressure.
• Example 414 1 H NMR (DMSO-of 6 ) ⁇ 8.26 (s, 1H), 8.23 (m, 1H), 8.13 (m, 1H),
• EXAMPLE 429 STEP A:
• R 2 H, or Cl
• EXAMPLE 431 Reactants: 3-Bromo-7-chloro-5-(2-chlorophenyl)pyrazolo[1 ,5- ajpyrimidine (110mg, 0.318mmoles) (prepared as described in Preparative Example 129); 3-(aminomethyl)piperidine-1-carboxamide (60mg, 0.382mmoles) (prepared as described in Preparative Example 241 above); diisopropyl ethylamine (0.111mL, 0.636mmoles); anhydrous 1 ,4-dioxane (2.5mL).
• HRFABMS m/z 463.0628 (MH + ). Calcd.
• EXAMPLE 432 Reactants: 3-Bromo-7-chloro-5-phenylpyrazolo[1 ,5-a]pyrimidine (500mg, 1.62mmoles) (prepared as described in Preparative Example 127); 3- (aminomethyl)piperidine-l-carboxamide (306mg, 1.944mmoles) (prepared as described in Preparative Example 241 above); diisopropyl ethylamine (0.566mL, 3.24mmoles); anhydrous 1 ,4-dioxane (13mL). Physical properties: HRFABMS: m/z 429.1031 (MH + ). Calcd.
• EXAMPLE 433 Reactants: 3-Bromo-7-chloro-5-(2-chlorophenyl)pyrazolo[1 ,5- ajpyrimidine (347mg, 1.01 mmoles) (prepared as described in Preparative
• Example 129 3-(aminoethyl)piperidine-1-carboxamide (208mg, 1.21 mmoles) (prepared as described in Preparative Example 242 above); diisopropyl ethylamine (0.393mL, 2.02mmoles); anhydrous 1 ,4-dioxane (9mL).
• EXAMPLE 434 Reactants: 3-Bromo-7-chloro-5-(2-chlorophenyl)pyrazolo[1 ,5- ajpyrimidine (275mg, 0.803mmoles) (prepared as described in Preparative Example 129); 4-(aminoethyl)piperidine-1-carboxamide (165mg, 0.963mmoles) (prepared as described in Preparative Example 243 above); diisopropyl ethylamine (0.311mL, 0.963mmoles); anhydrous 1 ,4-dioxane (7.2mL).
• EXAMPLE 435 Reactants: 3-Bromo-7-chloro-5-phenylpyrazolo[1 ,5-a]pyrimidine (174mg, 0.507mmoles) (prepared as described in Preparative Example 129) and 3-(aminomethyl)-1-methylpiperidine (65mg, 0.507mmoles) (prepared as described in Preparative Example 244 above); diisopropyl ethylamine (0.178mL, 1.014mmoles); anhydrous 1 ,4-dioxane (2.5mL).
• EXAMPLE 436 Reactants: 3-Bromo-7-chloro-5-phenylpyrazolo[1 ,5-a]pyrimidine (111.4mg, 0.325mmoles) (prepared as described in Preparative Example 129); 4-(aminomethyl)-1-methylpiperidine (50mg, 0.39mmoles) (prepared as described in Preparative Example 245 above); diisopropyl ethylamine (0.1135mL, 0.65mmoles); anhydrous 1 ,4-dioxane (1.5mL).
• EXAMPLE 437 Reactants: 3-Bromo-7-chloro-5-phenylpyrazolo[1 ,5-a]pyrimidine (191mg, 0.557mmoles) (prepared as described in Preparative Example 129); 3- (aminomethyl)benzonitrile (88.3mg, 0.668mmoles) (prepared as described in Preparative Example 246 above); diisopropyl ethylamine (0.192mL, 1.114mmoles); anhydrous 1 ,4-dioxane (4.5mL).
• EXAMPLE 438 Reactants: 3-Bromo-7-chloro-5-phenylpyrazolo[1 ,5-a]pyrimidine (233.5mg, 0.681 mmoles) (prepared as described in Preparative Example 129); 4-(aminomethyl)benzonitrile (108mg, 0.817mmoles) (prepared as described in Preparative Example 247 above); diisopropyl ethylamine (0.235mL, 1.362mmoles); anhydrous 1,4-dioxane (5.3mL).
• 3-Bromo-7-chloro-5-(2-chlorophenyl)pyrazolo[1 ,5-a]pyrimidine (50mg, 0.146mmoles) (prepared as described in Preparative Example 129) was dissolved in anhydrous 1 ,4-dioxane (5mL) in a GeneVac Technologies carousel reaction tube.
• PS-diisopropyl ethylamine resin (161mg, 0.5828mmoles) was added to each tube.
• EXAMPLE 440 Physical properties: HRFABMS: m/z 428.0272 (MH + ). Calcd. for Ci 9 H 16 N 5 BrCI: m/z 428.0278; ⁇ H (CDCI 3 ) 3.28 (2H, dd, C 5 H 4 NCH 2 CH 2 NH-), 3.94 (2H, ddd, C 5 H 4 NCH 2 CH 2 NH-), 6.40 (1H, s, H 6 ), 7.22-7.29 (3H, m, Ar-H), 7.38- 7.44 (2H, m, Ar-H), 7.51 (1 H, m, Ar-H), 7.68 (1 H, ddd, Ar-H), 7.73 (1 H, Ar-H), 8.18 (1 H, s, H 2 ) and 8.68ppm (1H, NH); ⁇ c (CDCI3) CH 2 : 36.4, 41.5; CH: 87.3, 122.1 , 123.6, 127.1 , 130.1, 130.1 , 131.6, 137.0, 143.8,
• EXAMPLE 442 Physical properties: HRFABMS: m/z 428.0275 (MH + ). Calcd. for Ci9H 16 N 5 BrCI: m/z 428.0278; ⁇ H (CDCI 3 ) 3.13 (2H, dd, C 5 H 4 NCH2CH 2 NH-), 3.80 (2H, ddd, C 5 H 4 NCH 2 CH 2 NH-), 6.42 (1 H, s, H 6 ), 6.53 (1 H, m, Ar-H), 7.23 (2H, m, Ar-H), 7.40-7.46 (2H, m, Ar-H), 7.62 (1 H, m, Ar-H), 7.76 (1 H, m, Ar-H), 8.07 (1 H, s, H 2 ) and 8.63ppm (1H, m, NH); ⁇ c (CDCI 3 ) CH 2 : 34.7, 42.5; CH: 87.4, 124.5,
• EXAMPLE 445 Physical properties: HRFABMS: m/z 448.0910 (MH + ). Calcd. for C 2 oH 2 . N 5 BrCI: m/z 448.0904; ⁇ H (CDCI 3 ) 1.90 (4H, m, CH 2 ), 2.00 (4H, m, CH 2 ), 2.84 (2H, m, CH 2 ), 2.95 (4H, m, CH 2 ), 3.51 (2H, m, CH 2 ), 6.32 (1 H, s, H 6 ), 7.05 (1 H, bm, NH), 7.37-7.43 (2H, m, Ar-H), 7.50 (1 H, m, Ar-H), 7.73 (1 H, m, Ar-H) and 8.04 ppm (1H, s, H 2 ); ⁇ c (CDCI3) CH 2 : 23.4, 23.4, 24.8, 26.4, 41.8, 53.9, 53.9, 55.2; CH: 87.3, 127.1, 130.1 , 130.2,
• 3-Bromo-7-chloro-5-(2-chlorophenyl)pyrazolo[1,5-a]pyrimidine (50mg, 0.146mmoles) (prepared as described in Preparative Example 129) was dissolved in anhydrous 1 ,4-dioxane (5mL) in a GeneVac Technologies carousel reaction tube.
• PS-diisopropyl ethylamine resin (161mg, 0.5828mmoles) was added to each tube.
• EXAMPLE 456 This enantiomer may be prepared by essentially the same manner as described above.
• Example 476-479 A mixture of the compound prepared in Example 129 (300 mg, 0.66 mmol), NaOH (5 g), CH 3 OH -H 2 O (100 mL, 90:10) was stirred at 25 C for about 15 h. Progress of hydrolysis was checked by TLC. Reaction mixture was concentrated to remove methanol. The concentrate was diluted with 50 mL water, and extracted with ether to remove any un-reacted ester. Aqueous solution, thus obtained, was neutralized with 3 N HCl to pH 4 to obtain free acid, filtered and washed repeatedly with water. The acid was dried under vacuum ( 270 mg, 93% ) and used without further purification.
• Example 476-479 A mixture of the compound prepared in Example 129 (300 mg, 0.66 mmol), NaOH (5 g), CH 3 OH -H 2 O (100 mL, 90:10) was stirred at 25 C for about 15 h. Progress of hydrolysis was checked by TLC. Reaction mixture was concentrated to remove methanol. The concentrate was diluted with
• Example 476 1 H NMR (CDCI 3 ) ⁇ 8.15 (m, 2H), 8.0 (m, 1 H), 7.6 (m, 1H), 7.3 (m,
• Example 477 1 H NMR (CDC l 3 ) ⁇ 8.15 (dt, 1H), 8.0 (s, 1 H), 7.4 (m, 1H), 7.25 (dd,
• Example 479 1 H NMR (CDCI 3 ) ⁇ 8.15 (dt, 1H), 8.0 (s, 1H), 7.4 (m, 1H), 7.25 (dd,
• Example 480 By essentially the same procedure set forth in Example 480 only substituting the carboxylic acid shown in Column 2 of Table 40 and the amine shown in Column 3 of Table 40, the compounds shown in Column 4 of Table 40 were prepared.
• Example 481 1 H NMR (CDCI 3 ) ⁇ 8.15 (dt, 1H), 8.0 (s, 1H), 7.7 (d, 2H), 7.4 (s,
• Example 482 1 H NMR (CDCI 3 ) ⁇ 8.15 (dt, 1 H),8.0 (s, 1 H), 7.45 - 7.35 (m, 4H),
• Example 483 1 H NMR (CDCI 3 ) ⁇ 8.15 (dt, 1H), 8.0 (s, 1H), 7.8 (bs, 1H), 7.7 (d,
• Example 484 1 H NMR (CDCI3) ⁇ 8.15 (dt, 1H), 8.0 (s, 1H), 7.7 (d, 2H), 7.4 (d,
• Example 486 1 H NMR (CDCI3) ⁇ 8.15 (dt, 1H), 8.0 (s, 1H), 7.8 (d, 2H), 7.4 (d, 2H), 7.35 (d, 1H), 7.25 (dd, 1H), 7.1 (dd, 1H), 6.9 (t, 1H), 6.5 (s, 1H), 6.2 (t, 1H), 4.7 (d, 2H), 3.3 (dd, 2H), 1.05 (m, 1H), 0.5 (m, 2H), 0.25 (m, 2H).
• Example 487 1 H NMR (CDCI 3 ) ⁇ 8.15 (dt, 1H), 8.0 (s, 1H), 7.7 (d, 2H), 7.4 (d, 2H), 7.35 (m, 1H), 7.25 (dd, 1H), 7.15 (dd, 1H), 6.85 (t, 1H), 6.5 (s, 1H), 6.2 (bs, 1H), 4.7 (d, 2H), 4.6 (m, 1H), 2.4 (m, 2H), 1.95 (m, 1H), 1.75 (m, 2H).
• Example 488 1 H NMR (CDCI3) ⁇ 8.5 (t, 1H), 8.15 (dt, 1H), 8.0 (s, 1H), 7.7 (d, 2H), 7.4 (d, 2H), 7.35 (m, 1H), 7.25 (dd, 1H), 7.15 (dd, 1H), 6.8 (t, 1H), 6.5 (s, 1H), 5.9 (bs, 1H), 4.7 (d, 2H), 1.4 (s, 9H).
• Example 489 1 H NMR (CDCI 3 ) ⁇ 8.15 (dt, 1H), 8.0 (s, 1H), 7.7 (d, 2H), 7.4 (d, 2H), 7.35 (m, 1H), 7.25 (dd, 1H), 7.15 (dd, 1H), 6.8 (t, 1H), 6.5 (s, 1H), 6.0 bs, 1 H), 4.7 (d, 2H), 4.4 (m, 1 H), 2.05 (m, 2H), 1.7 (m, 4H), 1.4 (m, 2H).
• Example 490 1 H NMR (CDCI3) ⁇ 8.15 (dt, 1H), 8.0 (s, 1H), 7.7 (d, 2H), 7.4 (d, 2H), 7.35 (m, 1H), 7.25 (dd, 1H), 7.15 (dd, 1H), 6.8 (t, 1H), 6.5 (s, 1H), 6.5 (bs, 2H), 4.7 (d, 2H), 4.1 (m, 1H), 3.9 - 3.7 (m, 3H), 3.3 (m, 1H), 2.0 - 1.9 (m, 4H).
• Example 491 1 H NMR (CDCI 3 ) ⁇ 8.15 (dt, 1H), 8.0 (s, 1H), 7.45 - 7.35 (m, 5H), 7.25 (dd, 1 H), 7.1 (dd, 1 H), 6.8 (t, 1 H), 6.5 (s, 1 H), 4.7 (d, 2H), 3.7 (bs, 2H),3.3 ( bs, 2H), 1.7 (bs, 4H), 1.5 (bs, 2H).
• Example 492 1 H NMR (CDCI 3 ) ⁇ 8.15 (dt, 1 H), 8.0 (s, 1 H), 7.45 - 7.35 (m, 5H), 7.25 (dd, 1 H), 7.1 (dd, 1 H), 6.85 (t, 1 H), 6.5 (s, 1 H), 4.7 (d, 2H), 3.8 - 3.4 (bm, 8H).
• Example 493 1 H NMR (CDCI 3 ) ⁇ 8.15 (dt, 1H), 8.0 (s, 1H), 7.45 - 7.35 (m, 5H), 7.25 (dd, 1H), 7.1 (dd, 1H), 6.80 (t, 1H), 6.5 (s, 1H), 4.7 (d, 2H), 4.0 (m, 2H), 3.6 (m,2H), 2.8 -2.45 (m,4H).
• Example 494 1 H NMR (CH3OD) ⁇ 8.15 (s, 1 H), 8.0 (dt, 1 H), 7.45 - 7.35 (m, 5H), 7.25 (dd, 1H), 7.1 (dd, 1H), 6.80 (t, 1H), 6.5 (s, 1H), 4.7 (d, 2H), 3.7 (bs, 2H), 3.4 (bs, 2H), 2.5 - 2.4 (m, 4H), 2.2 (s, 3H).
• Example 495 1 H NMR (CDCI 3 ) ⁇ 8.15 (dt, 1H), 8.0 (s, 1H), 7.45-7.35 (m, 5H),
• Example 496 1 H NMR (CDCI 3 ) ⁇ 7.95 (s, 1H), 7.9 (dt, 1H), 7.8 (t, 1H), 7.7 (d, 2H), 7.15 (m, 4H), 7.05 (dd,1H), 6.9 (dd, 1H), 6.2 (s,1H), 4.5 (d, 2H), 3.6 (t, 2H),
• Example 500 1 H NMR (CH3OD) ⁇ 8.15 (s, 1H), 7.9 (dt, 1H), 7.8 (d, 2H), 7.45 (d,
• Example 501 1 H NMR (CDCI 3 ) ⁇ 8.05 (dt, 1H), 8.0 (s, 1H), 7.6 (d, 2H), 7.4 (s, 1H), 7.35 (d, 2H), 7.25 (dd, 1H), 7.1 (dd, 1H), 6.9 (t, 1H), 6.5 (s, 1H), 6.4 (t,1H),
• Example 502 1 H NMR (CDCI 3 ) ⁇ 8.15 (dt, 1H), 8.0 (s, 1H), 7.75 (d, 2H), 7.45 (s,
• Example 504 1 H NMR (CDCI 3 ) ⁇ 8.15 (dt, 1H), 8.0 (s, 1H), 7.8 (d, 2H), 7.45 (d,
• Example 506 1 H NMR (CDCI 3 ) ⁇ 8.15 (dt, 1H), 8.0 (s, 1 H), 7.4 (m, 1 H), 7.25 (dd,
• Example 507 1 H NMR (CDCI3) ⁇ 8.15 (dt, 1H), 8.0 (s, 1H), 7.4 (m, 1H), 7.25 (dd,
• Example 508 1 H NMR (CH 3 OD ) ⁇ 8.1 (s, 1H), 7.95 (dt, 1 H), 7.5 (m, 1 H), 7.35 -

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