Classifications

• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
  • C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
  • C07D487/04—Ortho-condensed systems
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K31/00—Medicinal preparations containing organic active ingredients
  • A61K31/33—Heterocyclic compounds
  • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
  • A61K31/495—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
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K31/00—Medicinal preparations containing organic active ingredients
  • A61K31/33—Heterocyclic compounds
  • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
  • A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
  • A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
  • A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P19/00—Drugs for skeletal disorders
  • A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P25/00—Drugs for disorders of the nervous system
  • 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
  • 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

Definitions

• 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.
• CDKs cyclin-dependent kinases
• MAPK/ERK mitogen activated protein kinase
• GSK3beta glycogen synthase kinase 3
• the cyclin-dependent kinases are serine/threonine protein kinases, which are the driving force behind the cell cycle and cell proliferation.
• Individual CDK's such as, 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).
• 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 - heteroaryl,
• 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 2 wherein one or more of the aryl and/or one or more of the heteroaryl in the above-noted definitions for R 2 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, -CN, -OR 5 , -SR 5 ,
• R 3 is selected from the group consisting of H, halogen, -NR 5 R 6 , -OR 6 ,
• R 4 is H, halo or alkyl
• R 5 is H, alkyl, aryl or cycloalkyl
• R 6 is selected from the group consisting of H, alkyl, alkenyl, aryl, arylalkyl, arylalkenyl, cycloalkyl, heterocyclyl, heterocyclylalkyl, heteroaryl, and heteroarylalkyl, wherein each of said alkyl, aryl, arylalkyl, cycloalkyl, heterocyclyl, heterocyclylalkyl, heteroaryl, and heteroarylalkyl 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, alky
• R 5 and R 10 in the moiety -NR 5 R 10 , or (ii) R 5 and R 6 in the moiety -NR 5 R 6 may be joined together to form a cycloalkyl or heterocyclyl moiety, with each of said cycloalkyl or heterocyclyl moiety being unsubstituted or optionally independently being substituted with one or more R 9 groups
• 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, -NR 5 R 6 ,
• R 4 is H or lower alkyl.
• R 5 is H, lower alkyl or cycloalkyl.
• n is 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.
• n is 1.
• 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). Table 1
• Another embodiment of the invention discloses the following compounds, which exhibited CDK2 inhibitory activity of about 0.0001 ⁇ M to about 0.5 ⁇ M:
• Another embodiment of the invention discloses the following compounds, which exhibited CDK2 inhibitory activity of about 0.0001 ⁇ M to about 0.1 ⁇ M: ,,,,. ,.' , discipline » '
• 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.
• 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.
• 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 heteroaryls contain about 5 to about 6 ring atoms.
• heteroaryl can be optionally substituted by one or more "ring system substituents" which may be the same or different, and are as defined herein.
• 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.
• Non-limiting examples of 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, benzothienyl, quinolinyl, imidazolyl, thienopyridy
• heteroaryl also refers to partially saturated heteroaryl moieties such as, for example, tetrahydroisoquinolyl, tetrahydroquinolyl and the like.
• “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, alkylheteroaryl, hydroxy, hydroxyalkyl, alkoxy, aryl ⁇ xy, aralkoxy, acyl, aroyl, halo, nitro, cyano, carboxy, alkoxycarbonyl, aryloxycarbonyl, aralkoxycarbonyl, alkylsulfonyl, arylsulfonyl, heteroarylsulfonyl, alkylthio, arylthio, heteroarylthio, aralkyl
• 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 a d/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. It should be noted that in 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. Thus, for example, in the ring:
• 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-alkylr 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.
• Non-limiting examples of 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.
• Aralkyloxy 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.
• Non-limiting examples of 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.
• Aralkylthio 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. Non-limiting examples of suitable aryloxycarbonyl groups include phenoxycarbonyl and naphthoxycarbonyl. The bond to the parent moiety is through the carbonyl.
• Aralkoxycarbonyl means an aralkyl-O-C(O)- group. Non-limiting example of a suitable aralkoxycarbonyl group is benzyloxycarbonyl.
• 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.
• 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. 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.
• any 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.
• prodrug 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 II"" l n II .' 40 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 5 with one or more solvent molecules.
• 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.
• suitable solvates include ethanolates, methanolates, and the like.
• Hydrophile 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, 15 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)", as employed herein, denotes acidic salts formed with inorganic 20 and/or organic acids, as well as basic salts formed ith inorganic and/or organic bases.
• zwitterions 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 30 lyophilization.
• exemplary acid addition salts include acetates, ascorbates, benzoates, benzenesulfonates, bisulfates, borates, butyrates, citrates, camphorates, "' [, shadow calls "•” '
• 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. 5 Additionally, acids which are generally considered suitable for the formation of pharmaceutically useful salts from basic pharmaceutical compounds are discussed, for example, by S. Berge et al, Journal of Pharmaceutical Sciences (1977) 66(1 ) 1-19; P.
• Exemplary basic salts include ammonium salts, alkali metal salts such as sodium, lithium, and potassium salts, alkaline earth metal salts such as calcium 15 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
• 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), such as 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/neurodegenerative 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/neurodegenerative 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/neurodegenerative disorders, arthritis, inflammation, anti-proliferative (e.g., ocular retinopathy), neuronal, alopecia and cardiovascular disease.
• 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 " ⁇ -i;;'.! * .
• 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 lymphocy
• 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 5 leukemia; tumors of mesenchymal origin, including fibrosarcoma and rhabdomyosarcoma; tumors of the central and peripheral nervous system, including astrocytoma, neuroblastoma, glioma and schwannomas; and 10 other tumors, including melanoma, seminoma, teratocarcinoma, osteosarcoma, xenoderoma pigmentosum, keratoctanthoma, thyroid follicular cancer and
• inhibitors could act as reversible cytostatic agents which may be useful 15 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 20 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 20 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 25 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, 30 autoimmune diseases (including but not limited to systemic lupus, erythematosus, autoimmune mediated glomerulonephritis, rheumatoid arthritis, psoriasis, inflammatory bowel disease, and autoimmune diabetes mellitus), ,, ⁇ ,,, negligence ,. ⁇
• 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
• myelodysplastic syndromes including aplastic anemia, ischemic injury associated with myocardial infarctions, stroke and reperfusion injury, arrhythmia, atherosclerosis, toxin-induced or alcohol related liver diseases, hematological diseases (including but not limited to chronic anemia and aplastic anemia), degenerative diseases of the musculoskeletal system (including but not limited to osteoporosis and arthritis) aspirin-sensitive rhinosinusitis, cystic fibrosis, multiple sclerosis, kidney diseases and cancer pain.
• 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).
• Compounds of Formula III may also be useful in the chemoprevention of cancer. 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 ill 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.
• 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 preferred dosage is about 0.001 to 500 mg/kg of body weight/day of the ii,,,. II ,. ⁇ '' 'I...! 1 ' " "" " ' ' 45 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 5 (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 10 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 15 Schering-Plough Corporation, Kenilworth, New Jersey), cyclophosphamide); Famesyl 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 ,
• anti-cancer also known as anti-neoplastic
• anti-cancer agents include but are not limited to Uracil mustard, Chlormethine, Ifosfamide, Melphalan, Chlorambucil, Pipobroman, Triethylenemelamine, ,,, - 46 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, 5 Vincristine, Vindesine, Bleomycin, Dactinomycin, Daunorubicin, Doxorubicin, Epirubicin, Idarubicin, Mithramycin, Deoxycoformycin, Mitomycin-C, L
• the cytotoxic activity of the cyclin-dependent kinase inhibitor flavopiridol is affected by the sequence of administration with anticancer agents. Cancer Research, (1997) 57, 3375. Such techniques are within the skills of persons skilled in the art as well as attending physicians.
• 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 "" ii ⁇ ; II 'ii " ' 1 '• “ '
• the pharmacological properties of the compounds of this invention may be confirmed by a number of pharmacological assays. The exemplified 5 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 10 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 15 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.
• Liquid form preparations include solutions, suspensions and emulsions. As an example may be mentioned water or water-propylene glycol solutions for 25 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 30 acceptable carrier, such as an inert compressed gas, e.g. nitrogen.
• a pharmaceutically 30 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 " , nii. i"' 1 ' '""" " ' ' ' ' 48 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 5 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 or intravenously.
• 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 15 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 20 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.
• Another aspect of this invention is a kit comprising a therapeutically 30 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. il'" *' lt, memo ⁇ .
• kits 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 5 ingredients result in desired therapeutic effect.
• the invention disclosed herein is exemplified by the following preparations and examples which should not be construed to limit the scope of the disclosure. Alternative mechanistic pathways and analogous structures will be apparent to those skilled in the art.
• 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.
• Introduction of the N7-amino functionality can be accomplished through displacement of the chloride of compounds of type 9 by reaction with the appropriate amine as shown in Scheme 3. 'enfinchan. ,' ⁇ . 51 Scheme 3
• 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.
• PREPARATIVE EXAMPLE 20 O o o R OH R A ⁇ ⁇ 0Et To a solution of the acid in THF was added Et 3 N, followed by isobutyl chloroformate at -20 to -30°C. After the mixture was stirred for 30 min at -20 to -30°C, triethylamine hydrochloride was filtered off under argon, and the filtrate was added to the LDA-EtOAc reaction mixture (prepared as outlined in Method A) at -65 to -70°C. After addition of 1 N HCl, followed by routine workup of the reaction mixture and evaporation of the solvents, the crude ⁇ -keto esters were isolated. The crude material was used in the subsequent condensations.
• PREPARATIVE EXAMPLES 128-164 By essentially the same procedure set forth in Preparative Example 127 only substituting the compounds shown in Column 2 of Table 9, the compounds shown in Column 3 of Table 9 were prepared:
• PREPARATIVE EXAMPLE 166-167 By essentially the same procedure set forth in Preparative Example 165 only substituting the compound shown in Column 2 of Table 10, the compound shown in Column 3 of Table 10 was prepared: TABLE 10
• STEP B To a solution of amide (1.2 g, 6.12 mmol) from Preparative Example 206, Step A in THF (5 mL) at 0 °C was added a solution of BH 3 -THF (43 mL; 43 mmol) dropwise over 10 min. The resultant solution was warmed to rt and stirred for 14 h. The mixture was cooled to 0 °C and was sequentially treated with 6M HCl (35 mL), water (30 mL), and MeOH (150 mL). The mixture was stirred for 8 h and was concentrated under reduced pressure.
• STEP B A slurry of alcohol (31 g, 0.25 mol) from Preparative Example 216, Step A in CH 2 CI 2 (500 mL) was cooled to 0 °C and slowly treated with SOCI 2 (55mL, 0.74 mol over 30 minutes). The reaction was then stirred overnight at 20 °C. The material was concentrated, slurried in acetone, and then filtered. The resulting beige solid was dried overnight in vacuo (38.4g, 52%, HCl salt).
• STEP C To a 15 mL pressure tube charged with a stir bar was added chloride (150 mg, 0.83 mmol) from Preparative Example 216, Step B followed by 7 M NH 3 /MeOH (10 mL).
• PREPARATIVE EXAMPLE 219 The known amine dihydrochloride was prepared according to methods described in WO 02/64211. PREPARATIVE EXAMPLE 220:
• PREPARATIVE EXAMPLE 224 Pd(PPh 3 ) 4 ( 0.404 gm, 0.35 mmol ) was added to a degassed solution of 4-cyanobenzene boronic acid ( 1.029 g, 7 mmol ) and 2-bromopyridine ( 1.11 g, 7 mmol ) in 75 mL acetonitrile. 0.4 M sodium carbonate solution (35 mL ) was added to the reaction mixture and the resulting solution was refluxed at 90°C under Ar for 24 hours ( progress of reaction was monitored by TLC ). The reaction mixture was cooled and aqueous layer was separated. The organic layer containing the product and spent catalyst was mixed with silica gel ( 15 g ) and concentrated to dryness.
• 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 (1 M, 10 mL) slowly to the reaction mixture and refluxed for 5 h.
• 3(R/S)-(terf-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-fe/t-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.
• 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.
• the aldehyde was prepared according to the procedure of Gupton (J. Heterocyclic Chem. (1991 ), 28, 1281 ). PREPARATIVE EXAMPLE 255
• 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, 1 H), 7.1 (dd, 1 H), 7.0 (t, 1 H), 6.6 (s, 1H),4.8(d, 2H).
• Example 127 1 H NMR (CDCI 3 ) ⁇ 8.2 (dt, 1 H), 8.0 (s,1 H), 7.4 (dd, 1 H), 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, 1 H), 8.0 (s,1 H), 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 134 1 H NMR (CDCI3) ⁇ 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,1H), 8.0 (t, 1H), 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 (CDCI3) ⁇ 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 (CDCI3) ⁇ 8.2 (dt, 1 H), 8.0 (s, 1 H), 7.4 (m, 1 H), 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 (CDCI3) ⁇ 8.2 (dt, 1H), 8.0 (s, 1H), 7.9 (d,1H), 7.8 (d, 1H), 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 (CDCI3) ⁇ 8.2 (dt, 1 H), 8.0 (s, 1 H), 7.4 (m, 1 H), 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 (CDCI3) ⁇ 8.45 (s, 1H), 8.2 (dt, 1H), 8.0 (s, 1H), 7.7 (dd, 1H), 7.4 - 7.3 (m, 3H), 7.15 (dd, 1H), 6.8 (t, 1H), 6.6 (s,1H), 4.7 (d, 2H)
• Example 141 1 H NMR (CDCI3) ⁇ 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 H NMR (DMSO-d 6 ) ⁇ 8.86 (s, 1H), 8.46 (s, 1H), 8.32-8.28 (m,
• Example 181 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 ) DD8.96 - 8.90 (s, 1H), 8.08 (s, 1H),
• 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, 1 H), 2.32-2.21 (m, 1 H).
• Example 199 1 H NMR (300MHz, CDCI 3 ) DD8.29 (s, 1 H), 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 ) D D 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 ) DD8.10 (s, 1 H), 8.08 (s, 1 H), 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 266 A solution of the compound prepared in Preparative Example 182 (26 mg, 0.070 mmol) and potassium thiocyanate (13 mg, 0.14 mmol) in MeOH (1 mL) was cooled in a cold water bath. To it was added a solution of bromine (22 mg, 0.14mmol) in MeOH (0.7 mL) dropwise. The resulting reaction mixture was stirred for 4 h at room temperature and the volatiles were removed under reduced pressure. The residue obtained was suspended in a small amount of CH 2 CI 2 . The potassium bromide was filtered off and pH of the filtrate was adjusted to about 7 by the addition of aqueous ammonia.
• 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 (0.1 g, 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.
• STEP B To a solution of thiomethyl derivative (60 mg, 0.14 mmol) from Example 338, Step A in dioxane (2 mL) was added Boc 2 O (61 mg, 0.28 mmol) followed by DMAP (21 mg, 0.17 mmol). The mixture was stirred for 14h at rt and was concentrated under reduced pressure.
• Step B Removal of the t-butoxycarbonyl protecting group with TFA
• TFA 0.54 mL, 7.0 mmol
• 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 B Removal to t-butoxycarbonyl protecting group with KOH.
• 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 CI 2 (2 x 4 mL). The combined organics were washed with brine, dried over Na 2 SO 4 , filtered, and concentrated under reduced pressure.
• Example 2 Utilizing the procedure outlined in Example 422, the amino compounds (Column 2) were converted to the corresponding methylsulfonamides (Column 3) in Table 34.
• Step A By essentially the same procedure set forth in Example 425, Step A only0 using tributylmethylethynyltin, the compound shown above was prepared.
• R 2 H, or CI
• EXAMPLE 431 Reactants: 3-Bromo-7-chloro-5-(2-chlorophenyl)pyrazolo[1 ,5- a]pyrimidine (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 (0.111 mL, 0.636mmoles); anhydrous 1 ,4-dioxane (2.5mL).
• HRFABMS m/z 463.0628 (MH + ).
• 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- a]pyrimidine (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- a]pyrimidine (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 (0.311 mL, 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
• 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).
• EXAMPLE 440 Physical properties: HRFABMS: m/z 428.0272 (MH + ). Calcd. for C 19 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 (1 H, 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 (1 H, NH); ⁇ c (CDCI 3 ) CH 2 : 36.4, 41.5; CH: 87.3, 122.1 , 123.6, 127.1 , 130.1 , 130.1 , 131.6, 137.0,
• EXAMPLE 442 Physical properties: HRFABMS: m/z 428.0275 (MH + ). Calcd. for C ⁇ 9 H ⁇ 6 N 5 BrCI: m/z 428.0278; ⁇ H (CDCI 3 ) 3.13 (2H, dd, C 5 H 4 NCH 2 CH 2 NH-), 3.80 (2H, ddd, C 5 H 4 NCH 2 CH2NH-), 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, ,, 3 U ⁇
• EXAMPLE 456 This enantiomer may be prepared by essentially the same manner as described above.
• EXAMPLE 460 4- ⁇ [3-BROMO-5-(2-CHLOROPHENYL)PYRAZOLO[1 ,5-a]PYRIMIDIN-7- YLAMINO]METHYL ⁇ PIPERIDINE-1 -CARBOXYLIC ACID AMIDE:
• Example 476-479 By essentially the same procedure set forth in Example 475 only substituting the compounds in Column 2 of Table 39, the compounds in Column 3 of Table 39 were prepared. Table 39
• Example 476 1 H NMR (CDCI 3 ) ⁇ 8.15 (m, 2H), 8.0 (m, 1 H), 7.6 (m, 1 H), 7.3 (m, 2H), 6.6 (s, 1H),4.2(d,2H).
• Example 477 1 H NMR (CDCI 3 ) ⁇ 8.15 (dt, 1H), 8.0 (s, 1H), 7.4 (m, 1H), 7.25 (dd, 1H), 7.15 (dd, 1H), 7.0 (t, 1H), 6.5 (s, 1H), 3.8 (dt, 2H), 2.6 (t, 2H).
• Example 479 1 H NMR (CDCI 3 ) ⁇ 8.15 (dt, 1H), 8.0 (s, 1H), 7.4 (m, 1H), 7.25 (dd, 1H), 7.15 (dd, 1H), 6.8 (t, 1H), 3.5 (dt, 2H), 2.4 (t, 2H), 1.8 (m, 4H).
• 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, 1H),8.0(s, 1H), 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 (CDCI 3 ) ⁇ 8.15 (dt, 1H), 8.0 (s, 1H), 7.7 (d, 2H), 7.4 (d,
• Example 486 1 H NMR (CDCI 3 ) ⁇ 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, 1 H), 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 (CDCI 3 ) ⁇ 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 (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), 6.5 (bs, 2H), 4.7 (d, 2H), 4.1 (m, 1 H), 3.9 - 3.7 (m, 3H), 3.3 (m, 1 H), 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, 1H), 8.0 (s, 1H), 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, 1 H), 8.0 (s, 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), 4.0 (m, 2H), 3.6 (m, 2H), 2.8 -2.45 (m,4H).
• Example 494 1 H NMR (CH3OD) ⁇ 8.15 (s, 1H), 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 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 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, 1 H), 7.35 (d, 2H), 7.25 (dd, 1 H), 7.1 (dd, 1 H), 6.9 (t, 1 H), 6.5 (s, 1 H), 6.4 (t,1 H),
• 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 (CDCI 3 ) ⁇ 8.15 (dt, 1H), 8.0 (s, 1 H), 7.4 (m, 1 H), 7.25 (dd,
• Example 508 1 H NMR (CH 3 OD ) ⁇ 8.1 (s, 1 H), 7.95 (dt, 1 H), 7.5 (m, 1 H), 7.35 -
• Example 534 1 H NMR (300MHz, CDCI 3 ) ⁇ 8.66 - 8.62 (s, 1 H), 8.62 - 8.58 (d, 1 H), 7.95 (s, 1 H), 7.72 - 7.68 (d, 1 H), 7.36 - 7.31 (dd, 1 H), 6.66 - 6.62 (t, 1 H), 5.93 (s, 1 H), 4.65 - 4.62 (d, 2H), 3.86 - 3.82 (d, 1 H), 3.65 - 3.58 (m, 1 H), 3.26 - 3.12 (dd, 4H), 3.02 - 2.80 (m, 3H), 2.10 - 2.00 (m, 1H), 1.67 - 1.57 (m, 3H).
• Example 535 1 H NMR (300MHz, CDCI 3 ) ⁇ 8.66 - 8.62 (s, 1 H), 8.62 - 8.58 (d, 1 H), 7.95 (s, 1 H), 7.72 - 7.67 (d, 1 H), 7.36 - 7.30 (dd, 1 H), 6.70 - 6.64 (t, 1 H), 5.90 (s, 1 H), 4.63 - 4.61 (d, 2H), 3.93 - 3.86 (m, 1 H), 3.69 - 3.61 (m, 4H), 3.27 - 3.23 (m, 4H), 3.10 - 3.01 (dd, 1 H), 2.93 - 2.84 (m, 2H), 2.08 - 2.03 (m, 1 H), 1.90 - 1.57 (m, 4H).
• Example 536 1 H NMR (300MHz, CDCI 3 ) ⁇ 8.67 (s, 1 H), 8.62 - 8.58 (d, 1 H), 7.96 (s, 1 H), 7.72 - 7.68 (d, 1 H), 7.36 - 7.30 (dd, 1 H), 6.79 - 6.72 (t, 1 H), 5.96 (s, 1 H), 4.86 (br s, 2H), 4.66 - 4.63 (d, 2H), 3.89 - 3.73 (m, 2H), 3.55 - 3.32 (m, 2H), 3.00 - 2.89 (m, 1 H), 2.10 - 1.97 (m, 2H), 1.70 - 1.53 (m, 2H).
• Example 537 1 H NMR (300MHz, CDCI 3 ) ⁇ 8.66 (s, 1 H), 8.62 - 8.58 (d, 1 H), 7.98 (s, 1 H), 7.77 - 7.76 (t, 1 H), 7.72 - 7.69 (d, 1 H), 7.63 - 7.59 (m, 1 H), 7.56 (s, 1 H), 7.36 - 7.29 (dd, 1 H), 6.83 - 6.79 (t, 1 H), 5.96 (s, 1 H), 4.67 - 4.64 (d, 2H), 3.98 - 3.93 (dd, 1 H), 3..79 - 3.68 (m, 2H), 3.37 - 3.28 (m, 1 H), 3.03 - 2.94 (m, 1 H), 2.12 - 1.99 (m, 1 H), 1.76 - 1.56 (m, 3H).
• Example 544 1 H NMR (300MHz, CDCI 3 ) ⁇ 8.66 - 8.62 (d, 1 H), 8.61 - 8.58 (dd, 1 H), 7.95 (s, 1 H), 7.72 - 7.67 (d, 1 H), 7.36 - 7.30 (dd, 1 H), 6.80 - 6.62 (br s, 1 H), 5.88 (s, 1 H), 4.63 (s, 2H), 3.08 - 2.95 (m, 2H), 2.87 - 2.80 (m, 2H), 2.04 (m, 1 H), 1.85 - 1.78 (m, 4H), 1.52 - 1.44 (m, 1 H), 0.87 - 0.82 (m, 2H), 0.72 - 0.66 (m, 2H).
• Example 545 1 H NMR (300MHz, CDCI 3 ) ⁇ 8.66 (s, 1 H), 8.62 - 8.58 (br t, 1 H), 7.97 (s, 1 H), 7.73 - 7.68 (d, 1 H), 7.36 - 7.30 (br t, 1 H), 6.79 - 6.72 (br t, 1 H), 5.96 (s, 1 H), 4.64 (br s, 2H), 4.59 - 4.46 (br d, 1 H), 3.95 - 3.74 ( br m, 1 H), 3.57
• Example 551 1 H NMR (300MHz, CDCI 3 ) ⁇ 8.67 (s, 1 H), 8.63 - 8.59 (d, 1 H), 7.96 (s, 1 H), 7.74 - 7.69 (d, 1 H), 7.36 - 7.30 (dd, 1 H), 6.69 - 6.64 (t, 1 H), 5.95 (s, 1 H), 4.67 - 4.63 (d, 2H), 3.85 3.65 (m,1 H), 3.75 - 3.65 (m, 1 H), 3.25 - 3.18 (dd, 1 H), 3.03 - 2.90 (m, 2H), 2.81 (s, 6H), 2.03 - 1.95 (m, 1 H), 1.89 - 1.68 (m, 3H).
• Example 552 1 H NMR (300MHz, CDCI 3 ) ⁇ 8.67 (s, 1 H), 8.62 - 8.59 (d, 1 H),
• Example 553 1 H NMR (300MHz, CDCI 3 ) ⁇ 8.67 (s, 1 H), 8.62 (br s, 1 H), 7.96 (s, 1 H), 7.74 - 7.69 (d, 1 H), 7.36 - 7.31 (dd, 1 H), 6.70 - 6.66 (t, 1 H), 5.98 (s, 1 H), 4.67 - 4.63 (d, 2H), 3.88 - 3.81 (m, 1 H), 3.71 - 3.65 (m, 1 H), 3.20 - 3.11 (dd, 1 H), 3.02 - 2.91 (m, 1 H), 2.90 - 2.80 (m, 4H), 2.01 - 1.80 (m, 3H).
• Example 559 1 H NMR (300MHz, CDCI 3 ) ⁇ 8.66 -8.60 (d, 1 H), 8.50 - 8.44 (dd, 1 H), 8.01 (s, 1 H), 7.93 (m, 1 H), 7.48 - 7.40 (dd, 1 H), 6.08 (s, 1 H), 4.80 - 7.74 (s, 2H), 4.32 -4.19 (br d, 2H), 3.10 - 2.86 (m, 2H), 1.95 - 1.68 (m, 4H).
• Example 563 1 H NMR (300MHz, CDCI 3 ) ⁇ 8.66 (s, 1 H), 8.62 - 8.58 (d, 1 H),
• the reaction mixture was agitated at room temperature for 16 h.
• the crude product solution was filtered into a reaction well loaded with trisamine resin (P-NH2, Argonaut Tech. Inc., 30 mg, 0.126 mmol) and isocyanate resin (P- NCO, Argonaut Tech. Inc., 35 mg, 0.063 mmol).
• the reaction mixture was agitated at room temperature for 16 h and filtered into the collection block.
• the product solution was evaporated under reduced pressure to afford the desired amide product.
• GENERAL PROCEDURE 2 Procedure for the sulfonamide formation parallel synthesis Parallel synthesis was conducted in polypropylene 96-well reaction blocks with removable top seal and fixed bottom seal. Each reaction well was fitted with a 20 micron polypropylene bottom frit and the maximum volume was 3 mL.
• the reaction mixture was agitated at room temperature for 3 days.
• the crude product solution was filtered into a reaction well loaded with sulfonic acid resin Lanterns (P-SO 3 H, MimotopesPty Ltd., 0.3 mmol).
• the reaction mixture was agitated at room temperature for.2 h and decanted.
• the product resin Lanterns were washed with methanol (1 mL) for three times.
• a solution of ammonia in methanol (2 M, 1.2 mL) was added.
• the reaction mixture was agitated at room temperature for 30 min. and filtered into the collection block.
• the product solution was evaporated under reduced pressure to afford the desired tertiary amine product.
• GENERAL PROCEDURE 5 Procedure for the parallel synthesis of 7,N- substituted pyrazolo[1 ,5a]pyrimidines
• GENERAL PROCEDURE 6 Procedure for the parallel synthesis of 5,N- substituted pyrazolo[1 ,5a]pyrimidines
• STEP B(acidic) The product from STEP A was taken up in 35% TFA DCM and agitated for 4 h followed by concentration under high vacuum. The residue was treated with 10% HCI(aq) in MeOH agitated for 2 h and then concentrated to give the desired product. . observed m/z 375.21.
• STEP B(basic) The product from step A was taken up in EtOH and treated with
• Ambersep ® 900-OH ion exchange resin (Acros, 100mg), heated at reflux for 48 h with gently stirring. The reaction mixture was cooled to rt, filtered and concentrated to provide the desired product.
• EXAMPLE 565 By utilizing the procedure set forth in General Procedure 1 and the compound from Example 462 shown below, the compounds with the observed m/z shown in Table 43 were prepared.
• EXAMPLE 566 By utilizing the procedure set forth in General Procedure 1 and the compound from Example 471 shown below, the compounds shown in Table 44 with the observed m/z were prepared.
• EXAMPLE 568 By utilizing the procedure set forth in General Procedure 1 and the compound from Example 513 shown below, the compounds shown in Table 46 with the observed m/z were prepared.
• EXAMPLE 569 By utilizing the procedure set forth in General Procedure 1 and the compound from Example 526 shown below, the compounds shown in Table 47 with the observed m/z were prepared.
• EXAMPLE 570 By utilizing the procedure set forth in General Procedure 1 and the compound from Example 524 shown below, the compounds shown in Table 48 with the observed m/z were prepared.
• EXAMPLE 571 By utilizing the procedure set forth in General Procedure 1 and the compound from Example 525 shown below, the compounds shown in Table 49 with the observed m/z were prepared.
• EXAMPLE 572 By utilizing the procedure set forth in General Procedure 1 and the compound from Example 526.10 shown below, the compounds shown in Table 50 with the observed m/z were prepared.
• EXAMPLE 573 By utilizing the procedure set forth in General Procedure 1 and the compound from Example 518 shown below, the compounds shown in Table 51 with the observed m/z were prepared.
• EXAMPLE 574 By utilizing the procedure set forth in General Procedure 1 and the compound from Example 519 shown below, the compounds shown in Table 52 with the observed m/z were prepared.
• EXAMPLE 575 By utilizing the procedure set forth in General Procedure 1 and the compound from Example 520 shown below, the compounds shown in Table 53 with the observed m/z were prepared.
• EXAMPLE 576 By utilizing the procedure set forth in General Procedure 1 and the compound from Example 522 shown below, the compounds shown in Table 54 with the observed m/z were prepared.
• EXAMPLE 577 By utilizing the procedure set forth in General Procedure 1 and the compound from Example 523 shown below, the compounds shown in Table 55 with the observed m/z were prepared.
• EXAMPLE 578 By utilizing the procedure set forth in General Procedure 2 and the compound from Example 462 shown below, the compounds shown in Table 56 with the observed m/z were prepared.
• EXAMPLE 579 By utilizing the procedure set forth in General Procedure 2 and the compound from Example 471 shown below, the compounds shown in Table 57 with the observed m/z were prepared.
• EXAMPLE 580 By utilizing the procedure set forth in General Procedure 2 and the compound from Example 515 shown below, the compounds shown in Table 58 with the observed m/z were prepared.
• EXAMPLE 581 By utilizing the procedure set forth in General Procedure 2 and the compound from Example 513 shown below, the compounds shown in Table 59 with the observed m/z were prepared.
• EXAMPLE 582 By utilizing the procedure set forth in General Procedure 2 and the compound from Example 513 shown below, the compounds shown in Table 60 with the observed m/z were prepared.
• EXAMPLE 583 By utilizing the procedure set forth in General Procedure 2 and the compound from Example 524 shown below, the compounds shown in Table 61 with the observed m/z were prepared.
• EXAMPLE 584 By utilizing the procedure set forth in General Procedure 2 and the compound from Example 525 shown below, the compounds shown in Table 62 with the observed m/z were prepared.
• EXAMPLE 585 By utilizing the procedure set forth in General Procedure 2 and the compound from Example 526.10 shown below, the compounds shown in Table 63 with the observed m/z were prepared.
• EXAMPLE 586 By utilizing the procedure set forth in General Procedure 2 and the compound from Example 518 shown below, the compounds shown in Table 64 with the observed m/z were prepared.
• EXAMPLE 587 By utilizing the procedure set forth in General Procedure 2 and the compound from Example 519 shown below, the compounds shown in Table 65 with the observed m/z were prepared.
• EXAMPLE 588 By utilizing the procedure set forth in General Procedure 2 and the compound from Example 520 shown below, the compounds shown in Table 67 with the observed m/z were prepared.
• EXAMPLE 590 By utilizing the procedure set forth in General Procedure 2 and the compound from Example 523 shown below, the compounds shown in Table 69 with the observed m/z were prepared.
• EXAMPLE 591 By utilizing the procedure set forth in General Procedure 3 and the compound from Example 462 shown below, the compounds shown in Table 70 with the observed m/z were prepared.
• EXAMPLE 592 By utilizing the procedure set forth in General Procedure 3 and the compound from Example 471 shown below, the compounds shown in Table 71 with the observed m/z were prepared.
• EXAMPLE 593 By utilizing the procedure set forth in General Procedure 3 and the compound from Example 513 shown below, the compounds shown in Table 72 with the observed m/z were prepared.
• EXAMPLE 594 By utilizing the procedure set forth in General Procedure 3 and the compound from Example 524 shown below, the compounds shown in Table 73 with the observed m/z were prepared.
• EXAMPLE 596 By utilizing the procedure set forth in General Procedure 3 and the compound from Example 519 shown below, the compounds shown in Table 75 with the observed m/z were prepared.
• EXAMPLE 600 By utilizing the procedure set forth in General Procedure 4 and the compound from Example 462 shown below, the compounds shown in Table 79 with the observed m/z were prepared.
• EXAMPLE 601 By utilizing the procedure set forth in General Procedure 4 and the compound from Example 471 shown below, the compounds shown in Table 80 with the observed m/z were prepared.
• EXAMPLE 602 By utilizing the procedure set forth in General Procedure 4 and the compound from Example 525 shown below, the compounds shown in Table 81 with the observed m/z were prepared.
• EXAMPLE 603 By utilizing the procedure set forth in General Procedure 4 and the compound from Example 526.10 shown below, the compounds shown in Table 82 with the observed m/z were prepared.
• EXAMPLE 604 By utilizing the procedure set forth in General Procedure 4 and the compound from Example 521 shown below, the compounds shown in Table 83 with the observed m/z were prepared.
• EXAMPLE 605 By utilizing the procedure set forth in General Procedure 4 and the compound from Example 523 shown below, the compounds shown in Table 84 with the observed m/z were prepared.
• EXAMPLE 606 By utilizing the procedure set forth in General Procedure 5 and the compound from Preparative Example 81 shown below, the compounds shown in Table 85 with the observed m/z were prepared.
• EXAMPLE 607 By utilizing the procedure set forth in General Procedure 6 and the compound from Preparative Example 196, the compounds shown in Table 86 with the observed m/z were prepared.
• Step A To a solution of 3-Br adduct (1.1 g, 4.1 mmol) from Preparative Example 142 in THF (40 mL) at 0 °C was added CH 3 SNa (0.32 g, 4.53 mmol) in one portion. The heterogenous mixture was stirred for 72 h at rt and the mixture was concentrated under reduced pressure. The crude product was partitioned between water (10 mL) and EtOAc (30 mL) and the layers were separated. The organic layer was washed with brine (1 x 10 mL) and dried (Na 2 SO 4 ).
• Step B To a solution of thiomethyl derivative (1.5 g, 5.37 mmol) from Step A in dioxane/DIPEA (15 mL/4 mL) at rt was added amino alcohol (1.3 g, 8.06 mmol) from Preparative Example 10. The mixture was heated at reflux for 48 h, cooled to rt, and concentrated under reduced pressure.
• Step C To a solution of thiomethyl derivative (2.2 g, 5.92 mmol) from Step B in CH 2 CI 2 (20 mL) at 0 °C was added MCPBA (1.53 g, 8.9 mmol) in one portion. The resulting mixture was stirred for 2h at 0 °C whereupon the mixture was diluted with CH 2 CI 2 (20 mL) and sat. aq. NaHCO 3 (15 mL).

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• 2004
  • 2004-02-11 US US10/776,988 patent/US7119200B2/en not_active Expired - Lifetime
• 2005
  • 2005-02-05 TW TW094104016A patent/TWI393566B/zh not_active IP Right Cessation
  • 2005-02-08 DE DE602005025733T patent/DE602005025733D1/de not_active Expired - Lifetime
  • 2005-02-08 RU RU2006132288/04A patent/RU2414472C9/ru active
  • 2005-02-08 JP JP2006553181A patent/JP4845743B2/ja not_active Expired - Lifetime
  • 2005-02-08 AT AT05722809T patent/ATE494287T1/de active
  • 2005-02-08 ES ES05722809T patent/ES2359410T3/es not_active Expired - Lifetime
  • 2005-02-08 CA CA2555345A patent/CA2555345C/en not_active Expired - Lifetime
  • 2005-02-08 BR BRPI0507644A patent/BRPI0507644B8/pt not_active IP Right Cessation
  • 2005-02-08 PL PL05722809T patent/PL1720882T3/pl unknown
  • 2005-02-08 DK DK05722809.0T patent/DK1720882T3/da active
  • 2005-02-08 MY MYPI20050514A patent/MY149044A/en unknown
  • 2005-02-08 CN CN2005800122934A patent/CN1946725B/zh not_active Expired - Lifetime
  • 2005-02-08 NZ NZ590480A patent/NZ590480A/en not_active IP Right Cessation
  • 2005-02-08 EP EP05722809A patent/EP1720882B1/en not_active Expired - Lifetime
  • 2005-02-08 KR KR1020067016132A patent/KR101196498B1/ko not_active Expired - Lifetime
  • 2005-02-08 AU AU2005212409A patent/AU2005212409C1/en not_active Expired
  • 2005-02-08 HR HR20110245T patent/HRP20110245T1/hr unknown
  • 2005-02-08 SI SI200531260T patent/SI1720882T1/sl unknown
  • 2005-02-08 WO PCT/US2005/003859 patent/WO2005077954A2/en not_active Ceased
  • 2005-02-10 PE PE2005000156A patent/PE20050774A1/es active IP Right Grant
  • 2005-02-10 AR ARP050100483A patent/AR047543A1/es active IP Right Grant
• 2006
  • 2006-03-31 US US11/396,079 patent/US20070054925A1/en not_active Abandoned
  • 2006-08-03 IL IL177283A patent/IL177283A/en active IP Right Grant
  • 2006-08-07 ZA ZA200606573A patent/ZA200606573B/xx unknown
  • 2006-09-08 NO NO20064046A patent/NO337520B1/no unknown
• 2010
  • 2010-07-09 JP JP2010157338A patent/JP2010215675A/ja not_active Withdrawn
• 2011
  • 2011-04-05 CY CY20111100349T patent/CY1112400T1/el unknown

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