The present invention relates to compounds which demonstrate antibacterial activity, processes for their preparation, pharmaceutical compositions containing them as the active ingredient, to their use as medicaments and to their use in the manufacture of medicaments for use in the treatment of bacterial infections in warm-blooded animals such as humans. In particular, this invention relates to compounds useful for the treatment of bacterial infections in warm-blooded animals such as humans, more particularly to the use of these compounds in the manufacture of medicaments for use in the treatment of bacterial infections in warm-blooded animals such as humans.
The international microbiological community continues to express serious concern that the evolution of antibiotic resistance could result in strains against which currently available antibacterial agents will be ineffective. In general, bacterial pathogens may be classified as either Gram-positive or Gram-negative pathogens. Antibiotic compounds with effective activity against both Gram-positive and Gram-negative pathogens are generally regarded as having a broad spectrum of activity.
Gram-positive pathogens, for example Staphylococci, Enterococci, Streptococci and mycobacteria, are particularly important because of the development of resistant strains which are both difficult to treat and difficult to eradicate from the hospital environment once established. Examples of such strains are methicillin resistant staphylococcus aureus (MRSA), methicillin resistant coagulase negative staphylococci (MRCNS), penicillin resistant Streptococcus pneumoniae and multiple resistant Enterococcus faecium.
The preferred clinically effective antibiotic for treatment of last resort of such resistant Gram-positive pathogens is vancomycin. Vancomycin is a glycopeptide and is associated with various toxicities, including nephrotoxicity. Furthermore, and most importantly, antibacterial resistance to vancomycin and other glycopeptides is also appearing. This resistance is increasing at a steady rate rendering these agents less and less effective in the treatment of Gram-positive pathogens. There is also now increasing resistance appearing towards agents such as β-lactams, quinolones and macrolides used for the treatment of upper respiratory tract infections, also caused by certain Gram negative strains including H. influenzae and M. catarrhalis.
Consequently, in order to overcome the threat of widespread multi-drug resistant organisms, there is an on-going need to develop new antibiotics, particularly those with either a novel mechanism of action and/or containing new pharmacophoric groups.
Deoxyribonucleic acid (DNA) gyrase is a member of the type II family of topoisomerases that control the topological state of DNA in cells (Champoux, J. J.; 2001. Ann. Rev. Biochem. 70: 369-413). Type II topoisomerases use the free energy from adenosine triphosphate (ATP) hydrolysis to alter the topology of DNA by introducing transient double-stranded breaks in the DNA, catalyzing strand passage through the break and resealing the DNA. DNA gyrase is an essential and conserved enzyme in bacteria and is unique among topoisomerases in its ability to introduce negative supercoils into DNA. The enzyme consists of two subunits, encoded by gyrA and gyrB, forming an A2B2 tetrameric complex. The A subunit of gyrase (GyrA) is involved in DNA breakage and resealing and contains a conserved tyrosine residue that forms the transient covalent link to DNA during strand passage. The B subunit (GyrB) catalyzes the hydrolysis of ATP and interacts with the A subunit to translate the free energy from hydrolysis to the conformational change in the enzyme that enables strand-passage and DNA resealing.
Another conserved and essential type II topoisomerase in bacteria, called topoisomerase IV, is primarily responsible for separating the linked closed circular bacterial chromosomes produced in replication. This enzyme is closely related to DNA gyrase and has a similar tetrameric structure formed from subunits homologous to Gyr A and to Gyr B. The overall sequence identity between gyrase and topoisomerase IV in different bacterial species is high. Therefore, compounds that target bacterial type II topoisomerases have the potential to inhibit two targets in cells, DNA gyrase and topoisomerase IV; as is the case for existing quinolone antibacterials (Maxwell, A. 1997, Trends Microbiol. 5: 102-109).
DNA gyrase is a well-validated target of antibacterials, including the quinolones and the coumarins. The quinolones (e.g. ciprofloxacin) are broad-spectrum antibacterials that inhibit the DNA breakage and reunion activity of the enzyme and trap the GyrA subunit covalently complexed with DNA (Drlica, K., and X. Zhao, 1997, Microbiol. Molec. Biol. Rev. 61: 377-392). Members of this class of antibacterials also inhibit topoisomerase IV and as a result, the primary target of these compounds varies among species. Although the quinolones are successful antibacterials, resistance generated primarily by mutations in the target (DNA gyrase and topoisomerase IV) is becoming an increasing problem in several organisms, including S. aureus and Streptococcus pneumoniae (Hooper, D. C., 2002, The Lancet Infectious Diseases 2: 530-538). In addition, quinolones, as a chemical class, suffer from toxic side effects, including arthropathy that prevents their use in children (Lipsky, B. A. and Baker, C. A., 1999, Clin. Infect. Dis. 28: 352-364). Furthermore, the potential for cardiotoxicity, as predicted by prolongation of the QTc interval, has been cited as a toxicity concern for quinolones.
There are several known natural product inhibitors of DNA gyrase that compete with ATP for binding the GyrB subunit (Maxwell, A. and Lawson, D. M. 2003, Curr. Topics in Med. Chem. 3: 283-303). The coumarins are natural products isolated from Streptomyces spp., examples of which are novobiocin, chlorobiocin and coumermycin A1. Although these compounds are potent inhibitors of DNA gyrase, their therapeutic utility is limited due to toxicity in eukaryotes and poor penetration in Gram-negative bacteria (Maxwell, A. 1997, Trends Microbiol. 5: 102-109). Another natural product class of compounds that targets the GyrB subunit is the cyclothialidines, which are isolated from Streptomyces filipensis (Watanabe, J. et al 1994, J. Antibiot. 47: 32-36). Despite potent activity against DNA gyrase, cyclothialidine is a poor antibacterial agent showing activity only against some eubacterial species (Nakada, N, 1993, Antimicrob. Agents Chemother. 37: 2656-2661).
Synthetic inhibitors that target the B subunit of DNA gyrase and topoisomeraselV are known in the art. For example, coumarin-containing compounds are described in patent application number WO 99/35155, 5,6-bicyclic heteroaromatic compounds are described in patent application WO 02/060879, and pyrazole compounds are described in patent application WO 01/52845 (U.S. Pat. No. 6,608,087). AstraZeneca has also published certain applications describing anti-bacterial compounds: WO2005/026149, WO2006/087544, WO2006/087548, WO2006/087543, WO2006/092599, WO2006/092608, WO2007/071965, WO2008/020227, WO2008/020222, WO2008/020229, WO2008/068470, and WO2008/152418.
We have discovered a new class of compounds which are useful for inhibiting DNA gyrase and/or topoisomerase IV. The compounds of the present invention are regarded as effective against both Gram-positive and certain Gram-negative pathogens.
In one embodiment, according to the present invention there is provided a compound of formula (I):
or a pharmaceutically acceptable salt thereof, wherein:
In a particular embodiment, the present invention provides compounds having a structural formula (I) as recited above, or a pharmaceutically acceptable salt thereof, wherein:
In another embodiment, the invention provides pharmaceutical compositions comprising a compound represented by formula (I), or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable excipient or carrier.
In another embodiment, the invention provides a method of inhibiting bacterial DNA gyrase and/or bacterial topoisomerase IV in a warm-blooded animal in need of such treatment, comprising administering to the animal an effective amount of a compound represented by formula (I), or a pharmaceutically acceptable salt thereof. In a particular embodiment, the warm-blooded animal is a human.
In another embodiment, the invention provides a method of producing an antibacterial effect in a warm-blooded animal in need of such treatment, comprising administering to the animal an effective amount of a compound represented by formula (I), or a pharmaceutically acceptable salt thereof. In a particular embodiment, the warm-blooded animal is a human.
In another embodiment, the invention provides a method of treating a bacterial infection in a warm-blooded animal in need thereof, comprising administering to the animal an effective amount of a compound represented by formula (I), or a pharmaceutically acceptable salt thereof. In a particular embodiment, the warm-blooded animal is a human. In one embodiment, the bacterial infection is selected from the group consisting of community-acquired pneumoniae, hospital-acquired pneumoniae, skin and skin structure infections, acute exacerbation of chronic bronchitis, acute sinusitis, acute otitis media, catheter-related sepsis, febrile neutropenia, osteomyelitis, endocarditis, urinary tract infections and infections caused by drug resistant bacteria such as Penicillin-resistant Streptococcus pneumoniae, methicillin-resistant Staphylococcus aureus, methicillin-resistant Staphylococcus epidermidis and Vancomycin-Resistant Enterococci. In a particular embodiment, the warm-blooded animal is a human.
In another embodiment, the invention provides the use of a compound represented by formula (I), or a pharmaceutically acceptable salt thereof, for the manufacture of a medicament for use in the production of an antibacterial effect in a warm-blooded animal. In a particular embodiment, the warm-blooded animal is a human.
In another embodiment, the invention provides the use of a compound represented by formula (I), or a pharmaceutically acceptable salt thereof, for the manufacture of a medicament for use in inhibition of bacterial DNA gyrase and/or topoisomerase IV in a warm-blooded animal. In a particular embodiment, the warm-blooded animal is a human.
In another embodiment, the invention provides the use of a compound represented by formula (I), or a pharmaceutically acceptable salt thereof, for the manufacture of a medicament for use the treatment of a bacterial infection in a warm-blooded animal. In one embodiment, the bacterial infection is selected from the group consisting of community-acquired pneumoniae, hospital-acquired pneumoniae, skin and skin structure infections, acute exacerbation of chronic bronchitis, acute sinusitis, acute otitis media, catheter-related sepsis, febrile neutropenia, osteomyelitis, endocarditis, urinary tract infections, Penicillin-resistant Streptococcus pneumoniae, methicillin-resistant Staphylococcus aureus, methicillin-resistant Staphylococcus epidermidis and Vancomycin-Resistant Enterococci. In a particular embodiment, the warm-blooded animal is a human.
In another embodiment, the invention provides a compound represented by formula (I), or a pharmaceutically acceptable salt thereof, for use in production of an anti-bacterial effect in a warm-blooded animal.
In another embodiment, the invention provides a compound represented by formula (I), or a pharmaceutically acceptable salt thereof, for use in inhibition of bacterial DNA gyrase and/or topoisomerase IV in a warm-blooded animal.
In another embodiment, the invention provides a compound represented by formula (I), or a pharmaceutically acceptable salt thereof, for use in the treatment of a bacterial infection in a warm-blooded animal.
In another embodiment, the invention provides a compound represented by formula (I), or a pharmaceutically acceptable salt thereof, for use in the treatment of community-acquired pneumoniae, hospital-acquired pneumoniae, skin and skin structure infections, acute exacerbation of chronic bronchitis, acute sinusitis, acute otitis media, catheter-related sepsis, febrile neutropenia, osteomyelitis, endocarditis, urinary tract infections, Penicillin-resistant Streptococcus pneumoniae, methicillin-resistant Staphylococcus aureus, methicillin-resistant Staphylococcus epidermidis or Vancomycin-Resistant Enterococci.
In this specification the term alkyl includes both straight chained and branched saturated hydrocarbon groups. For example, “C1-6alkyl” refers to an alkyl that has from 1 to 6 carbon atom and includes, for example, methyl, ethyl, propyl, isopropyl and t-butyl. However references to individual alkyl groups such as propyl are specific for the straight chain version only unless otherwise indicated (e.g., isopropyl). An analogous convention applies to other generic terms.
As used herein, the term “C1-6haloalkyl” refers to an alkyl group that has from 1 to 6 carbon atoms in which one or more of the carbon atoms are substituted with a halo group. Representative haloalkyl groups include —CF3, —CHF2, —CCl3, —CH2CH2Br, —CH2CH(CH2CH2Br)CH3, —CHICH3, and the like.
As used herein, the term “halo” refers to fluoro, chloro, bromo, and iodo.
A “heterocyclyl” is a saturated, partially saturated or unsaturated, mono or bicyclic ring containing 4-14 atoms of which at least one atom is chosen from nitrogen, sulphur or oxygen, which may, unless otherwise specified, be carbon or nitrogen linked, wherein a —CH2— group can optionally be replaced by a —C(O)— and a ring sulphur atom may be optionally oxidised to form the S-oxide(s). In one embodiment of the invention a “heterocyclyl” is a saturated, partially saturated or unsaturated, monocyclic ring containing 5 or 6 atoms of which at least one atom is chosen from nitrogen, sulphur or oxygen, it may, unless otherwise specified, be carbon or nitrogen linked, a —CH2— group can optionally be replaced by a —C(O)— and a ring sulphur atom may be optionally oxidised to form the S-oxides. In a further aspect of the invention a “heterocyclyl” is an unsaturated, carbon-linked, monocyclic ring containing 5 or 6 atoms of which at least one atom is chosen from nitrogen, sulphur or oxygen. Examples and suitable values of the term “heterocyclyl” are morpholinyl, piperidyl, pyridinyl, pyranyl, pyrrolyl, pyrazolyl, isothiazolyl, indolyl, quinolinyl, thienyl, 1,3-benzodioxolyl, benzothiazolyl, thiadiazolyl, oxadiazolyl, piperazinyl, thiazolidinyl, pyrrolidinyl, thiomorpholino, pyrrolinyl, homopiperazinyl, 3,5-dioxapiperidinyl, tetrahydropyranyl, imidazolyl, 4,5-dihydro-oxazolyl, pyrimidinyl, pyrazinyl, pyridazinyl, isoxazolyl, thiazolyl, 1H-tetrazolyl, 1H-triazolyl, N-methylpyrrolyl, 4-pyridone, quinolin-4(1H)-one, pyridin-2(1H)-one, imidazo[1,2-a]pyridinyl, 1-isoquinolone, 2-pyrrolidone, 4-thiazolidone, quinoxalinyl, 5,6-dihydro[1,3]thiazolo[4,5-d]pyridazinyl, pyridine-N-oxide and quinoline-N-oxide. Suitable examples of “a nitrogen linked heterocyclyl” are morpholino, piperazin-1-yl, piperidin-1-yl and imidazol-1-yl. The term “heterocyclyl” encompasses the term “heteroaryl.” A “heteroaryl” is an aromatic mono-, bi- or tricyclic heterocycle.
A “carbocyclyl” is a saturated, partially saturated or unsaturated, mono-, bi- or tricyclic carbon ring that contains 3-14 atoms; wherein a —CH2— group can optionally be replaced by a —C(O)—. In one embodiment, “carbocyclyl” is a monocyclic ring containing 5 or 6 atoms or a bicyclic ring containing 9 or 10 atoms. Examples of carbocyclyls include cyclopropyl, cyclobutyl, 1-oxocyclopentyl, cyclopentyl, cyclopentenyl, cyclohexyl, cyclohexenyl, phenyl, naphthyl, tetralinyl, indanyl or 1-oxoindanyl. The term carbocyclyl encompasses both cycloalkyl and aryl groups. The term cycloalkyl refers to a carbocyclyl which is completely saturated, for example cyclopropyl, cyclobutyl, cyclopentyl, and cyclohexyl. The term “aryl” refers to a carbocyclyl which is completely unsaturated and is aromatic. A C6-14aryl is an aromatic, mono-, bi- or tricyclic carbon ring that contains 6-14 atoms, for example phenyl or naphthenyl.
An example of “C1-6alkanoyloxy” is acetoxy. Examples of “C1-6alkoxycarbonyl” are methoxycarbonyl, ethoxycarbonyl, n- and t-butoxycarbonyl. Examples of “C1-6alkoxycarbonylamino” are methoxycarbonylamino, ethoxycarbonylamino, n- and t-butoxycarbonylamino Examples of “C1-6alkoxy” are methoxy, ethoxy and propoxy. Examples of “C1-6alkanoylamino” are formamido, acetamido and propionylamino Examples of “C1-6alkylS(O)a wherein a is 0, 1, or 2” are methylthio, ethylthio, methylsulphinyl, ethylsulphinyl, mesyl and ethylsulphonyl. Examples of “C1-6alkanoyl” are propionyl and acetyl. Examples of “N—(C1-6alkyl)amino” are methylamino and ethylamino Examples of “N,N—(C1-6alkyl)2amino” are di-N-methylamino, di-(N-ethyl)amino and N-ethyl-N-methylamino Examples of “C2-4alkenyl” are vinyl, allyl and 1-propenyl. Examples of “C2-4alkynyl” are ethynyl, 1-propynyl and 2-propynyl. Examples of “N—(C1-6alkyl)sulphamoyl” are N-(methyl)sulphamoyl and N-(ethyl)sulphamoyl. Examples of “N,N—(C1-6alkyl)2sulphamoyl” are N,N-(dimethyl)sulphamoyl and N-(methyl)-N-(ethyl)sulphamoyl. Examples of “N—(C1-6alkyl)carbamoyl” are methylaminocarbonyl and ethylaminocarbonyl. Examples of “N,N—(C1-6alkyl)2carbamoyl” are dimethylaminocarbonyl and methylethylaminocarbonyl. Examples of “N—(C1-6alkoxy)carbamoyl” are methoxyaminocarbonyl and isopropoxyaminocarbonyl. Examples of “N—(C1-6alkyl)-N—(C1-6alkoxy)carbamoyl” are N-methyl-N-methoxyaminocarbonyl and N-methyl-N-ethoxyaminocarbonyl. Examples of “C3-6cycloalkyl” are cyclopropyl, cyclobutyl, cyclopropyl and cyclohexyl. Examples of “C1-6alkylsulphonylamino” are methylsulphonylamino, isopropylsulphonylamino and t-butylsulphonylamino Examples of “C1-6alkylsulphonylaminocarbonyl” are methylsulphonylaminocarbonyl, isopropylsulphonylaminocarbonyl and t-butylsulphonylaminocarbonyl. Examples of “C1-6alkylsulphonyl” are methylsulphonyl, isopropylsulphonyl and t-butylsulphonyl.
A compound of formula (I) may form stable acid or basic salts, and in such cases administration of a compound as a salt may be appropriate, and pharmaceutically acceptable salts may be made by conventional methods such as those described below.
Suitable pharmaceutically-acceptable salts include acid addition salts such as methanesulfonate, tosylate, α-glycerophosphate, fumarate, hydrochloride, citrate, maleate, tartrate and (less preferably) hydrobromide. Also suitable are salts formed with phosphoric and sulfuric acid. In another aspect suitable salts are base salts such as an alkali metal salt for example sodium, an alkaline earth metal salt for example calcium or magnesium, an organic amine salt for example triethylamine, morpholine, N-methylpiperidine, N-ethylpiperidine, procaine, dibenzylamine, N,N-dibenzylethylamine, tris-(2-hydroxyethyl)amine, N-methyl d-glucamine and amino acids such as lysine. There may be more than one cation or anion depending on the number of charged functions and the valency of the cations or anions. A preferred pharmaceutically-acceptable salt is the sodium salt.
However, to facilitate isolation of the salt during preparation, salts which are less soluble in the chosen solvent may be preferred whether pharmaceutically-acceptable or not.
Within the present invention it is to be understood that a compound of the formula (I), or a salt thereof may exhibit the phenomenon of tautomerism and that the formulae drawings within this specification can represent only one of the possible tautomeric forms. It is to be understood that the invention encompasses any tautomeric form which inhibits DNA gyrase and/or topoisomerase IV and is not to be limited merely to any one tautomeric form utilised within the formulae drawings. The formulae drawings within this specification can represent only one of the possible tautomeric forms and it is to be understood that the specification encompasses all possible tautomeric forms of the compounds drawn not just those forms which it has been possible to show graphically herein. The same applies to compound names.
It will be appreciated by those skilled in the art that certain compounds of formula (I) contain an asymmetrically substituted carbon and/or sulphur atom, and accordingly may exist in, and be isolated in, optically-active and racemic forms. Some compounds may exhibit polymorphism. It is to be understood that the present invention encompasses any racemic, optically-active, polymorphic or stereoisomeric form, or mixtures thereof, which form possesses properties useful in the inhibition of DNA gyrase and/or topoisomerase IV, it being well known in the art how to prepare optically-active forms (for example, by resolution of the racemic form by recrystallization techniques, by synthesis from optically-active starting materials, by chiral synthesis, by enzymatic resolution, by biotransformation, or by chromatographic separation using a chiral stationary phase) and how to determine efficacy for the inhibition of DNA gyrase and/or topoisomerase IV by the standard tests described hereinafter.
By way of clarity, compounds of the invention included all isotopes of the atoms present in formula (I) and any of the examples or embodiments disclosed herein. For example, H (or hydrogen) represents any isotopic form of hydrogen including 1H, 2H (D), and 3H (T); C represents any isotopic form of carbon including 12C, 13C, and 14C; O represents any isotopic form of oxygen including 16O, 17O and 18O; N represents any isotopic form of nitrogen including 13N, 14N and 15N; P represents any isotopic form of phosphorous including 31P and 32P; S represents any isotopic form of sulfur including 32S and 35S; F represents any isotopic form of fluorine including 19F and 18F; Cl represents any isotopic form of chlorine including 35Cl, 37Cl and 36Cl; and the like. In a preferred embodiment, compounds represented by formula (I) comprises isomers of the atoms therein in their naturally occurring abundance. However, in certain instances, it is desirable to enrich one or more atom in a particular isotope which would normally be present in less abundance. For example, 1H would normally be present in greater than 99.98% abundance; however, a compound of the invention can be enriched in 2H or 3H at one or more positions where H is present. In particular embodiments of the compounds of formula (I), when, for example, hydrogen is enriched in the deuterium isotope, the symbol “D” may be used to represent the enrichment in deuterium. In one embodiment, when a compound of the invention is enriched in a radioactive isotope, for example 3H and 14C, they may be useful in drug and/or substrate tissue distribution assays. It is to be understood that the invention encompasses all such isotopic forms which inhibit DNA gyrase and/or topoisomerase IV.
It is also to be understood that certain compounds of the formula (I), and salts thereof can exist in solvated as well as unsolvated forms such as, for example, hydrated forms. It is to be understood that the invention encompasses all such solvated forms which inhibit DNA gyrase and/or topoisomerase IV.
There follow particular and suitable values for certain substituents and groups referred to in this specification. These values may be used where appropriate with any of the definitions and embodiments disclosed hereinbefore, or hereinafter. For the avoidance of doubt each stated species represents a particular and independent aspect of this invention.
In one embodiment the invention provides compounds represented by formula (I) wherein X is CH.
In another embodiment the invention provides compounds represented by formula (I) wherein X is N.
In another embodiment the invention provides compounds represented by formula (I) wherein X is CR4 and R4 is fluoro, chloro, bromo, iodo, a C1-4alkyl, or a C1-4alkoxy.
In another embodiment the invention provides compounds represented by formula (I) wherein ring B is a 5- or 6-membered heteroaryl, and wherein if said heteroaryl contains an —NH— moiety that nitrogen may be optionally substituted by a group selected from R15; and wherein if said heteroaryl contains an ═N— or a —S— moiety that nitrogen may be optionally substituted by one oxo group and that sulfur may be optionally substituted by one or two oxo groups.
In another embodiment the invention provides compounds represented by formula (I) wherein ring B is pyridinyl, pyrazinyl, pyrimidinyl or thiazolyl; and wherein each ═N— of pyridinyl, pyrazinyl, pyrimidinyl, or thiazolyl may be independently optionally substituted with one oxo group; and wherein the —S— moiety of the thiazolyl may be optionally by one or two oxo groups.
In another embodiment the invention provides compounds represented by formula (I) wherein ring B is pyridinyl, pyrazinyl, pyridazinyl, pyrimidinyl or thiazolyl; and wherein each ═N— of pyridinyl, pyrazinyl, pyrimidinyl, or thiazolyl may be independently optionally substituted with one oxo group; and wherein the —S— moiety of the thiazolyl may be optionally by one or two oxo groups.
In another embodiment the invention provides compounds represented by formula (I) wherein ring B is a bicyclic heterocyclyl; and wherein if said heterocyclyl contains an —NH— moiety that nitrogen may be optionally substituted by a group selected from R15; and wherein if said heterocyclyl contains an ═N— or a —S— moiety that nitrogen may be optionally substituted by one oxo group and that sulfur may be optionally substituted by one or two oxo groups.
In another embodiment the invention provides compounds represented by formula (I) wherein ring B is a quinoxalinyl or 5,6-dihydro[1,3]thiazolo[4,5-d]pyridazine-4,7-dione; and wherein each —NH— moiety of 5,6-dihydro[1,3]thiazolo[4,5-d]pyridazine-4,7-dione may be independently optionally substituted by a group selected from R15; and wherein each ═N— of quinoxalinyl or 5,6-dihydro[1,3]thiazolo[4,5-d]pyridazine-4,7-dione may be independently optionally substituted with one oxo group; and wherein the —S— moiety of the 5,6-dihydro[1,3]thiazolo[4,5-d]pyridazine-4,7-dione may be optionally by one or two oxo groups.
In another embodiment the invention provides compounds represented by formula (I) wherein ring B is a quinoxalinyl, 5,6-dihydro[1,3]thiazolo[4,5-d]pyridazine-4,7-dione or 2,3-dihydrophthalazine-1,4-dione; and wherein each —NH— moiety of 5,6-dihydro[1,3]thiazolo[4,5-d]pyridazine-4,7-dione or 2,3-dihydrophthalazine-1,4-dione may be independently optionally substituted by a group selected from R15; and wherein each ═N— of quinoxalinyl or 5,6-dihydro[1,3]thiazolo[4,5-d]pyridazine-4,7-dione may be independently optionally substituted with one oxo group; and wherein the —S— moiety of the 5,6-dihydro[1,3]thiazolo[4,5-d]pyridazine-4,7-dione may be optionally by one or two oxo groups.
In another embodiment the invention provides compounds represented by formula (I) wherein R1 is a C1-6alkyl which is optionally substituted by a halo. For example, R1 is methyl, ethyl, propyl, isopropyl, butyl, isobutyl, sec-butyl, and tert-butyl, 2,2,2-trifluoroethyl, or 2,2-difluoroethyl. In a particular embodiment, R1 is ethyl.
In another embodiment the invention provides compounds represented by formula (I) wherein R1 is a C1-6alkyl. For example, R1 is methyl, ethyl, propyl, isopropyl, butyl, isobutyl, sec-butyl, and tert-butyl. In a particular embodiment, R1 is ethyl.
In another embodiment the invention provides compounds represented by formula (I) wherein R1 is a C1-6alkyl which is substituted with a halo. For example, R1 is 2,2,2-trifluoroethyl or 2,2-difluoroethyl.
In another embodiment the invention provides compounds represented by formula (I) wherein R1 is a C3-6cylcoalkyl. For example, R1 is cyclopropyl or cyclohexyl.
In another embodiment the invention provides compounds represented by formula (I) wherein R2 is hydrogen.
In another embodiment the invention provides compounds represented by formula (I) wherein R2 is a C1-6alkyl. For example, R2 is methyl, ethyl, propyl, isopropyl, butyl, isobutyl, sec-butyl, and tert-butyl.
In another embodiment the invention provides compounds represented by formula (I) wherein R3 is a 5-membered heteroaryl; and wherein the heteroaryl may be optionally substituted on one or more carbon atoms by one or more R10; and wherein if said heteroaryl contains an ═N— or a —S— moiety that nitrogen may be optionally substituted by one oxo group and that sulfur may be optionally substituted by one or two oxo groups; and wherein if said heteroaryl contains an —NH— moiety that nitrogen may be optionally substituted by a group selected from R11. In one aspect of this embodiment, R10, for each occurrence, is selected from the group consisting of methyl, phenyl, trifluoromethyl, and pyridinyl. In another aspect of this embodiment, R11 is methyl.
In another embodiment the invention provides compounds represented by formula (I) wherein R3 is a thiazolyl; and wherein the thiazolyl may be optionally substituted on carbon by one or more R10; and wherein the ═N— of the thiazolyl may be optionally substituted by one oxo group; and wherein the —S— of the thiazolyl may be optionally substituted by one or two oxo groups. In one aspect of this embodiment, R10, for each occurrence, is independently selected from the group consisting of methyl, phenyl, trifluoromethyl, and pyridinyl. In one aspect of this embodiment, R10, for each occurrence, is independently selected from the group consisting of methyl, phenyl, trifluoromethyl, pyridinyl, 1-methyl-1H-pyrazol-4-yl, N-(2-morpholinoethyl)aminomethyl, N-cyclohexylaminomethyl, cyclopentylaminomethyl, N-(2-methoxyethyl)aminomethyl, N-(tetrahydro-2H-pyran-4-yl)aminomethyl, N-(2-methoxyethyl)-carbamoyl, N-(2-morpholinoethyl)-carbamoyl, N-[2-(N-methyl-piperazino)-ethyl]-carbamoyl, N-cyclopropyl-carbamoyl, N-cyclopentyl-carbamoyl, N-cyclohexyl-carbamoyl, methoxy, 6-methoxypyridin-2-yl, 6-methoxypyridin-3-yl, 2-fluoropyridin-3-yl, 2-(2-methoxyethoxy)pyridin-2-yl, 6-methoxypyridin-2-yl, pyridin-4-ylmethyl, cyclopropyl, 2,2-dimethyl-2H-tetrahydropyran-4-yl, N-(1H-imidazol-1-ylcarbonyl)-piperidin-4-yl, cyclopentyl, and cyclohexyl. In another aspect R10 is trifluoromethyl.
In another embodiment the invention provides compounds represented by formula (I) wherein R3 is a 1,3,4-oxadiazolyl; and wherein the 1,3,4-oxadiazolyl may be optionally substituted on one or more carbon by one or more R10; and wherein each ═N— of the 1,3,4-oxadiazolyl may be independently optionally substituted by one oxo group. In one aspect of this embodiment, R10, for each occurrence, is independently selected from the group consisting of methyl, phenyl, trifluoromethyl, and pyridinyl. In another aspect of this embodiment, R10, for each occurrence, is selected from pyridinyl, phenyl, and 4-fluorophenyl.
In another embodiment the invention provides compounds represented by formula (I) wherein R3 is a 1H-pyrazolyl; and wherein the 1H-pyrazolyl may be optionally substituted on one or more carbon by one or more R10; and wherein the ═N— of the 1H-pyrazolyl may be optionally substituted by one oxo group; and wherein the —NH— moiety of the 1H-pyrazolyl may be optionally substituted by a group selected from R11. In one aspect of this embodiment, R10, for each occurrence, is independently selected from the group consisting of methyl, phenyl, trifluoromethyl, and pyridinyl. In another aspect of this embodiment, R11 is methyl. In another aspect of this embodiment, R11 is methyl, 2-morpholinoethyl, or isopropyl.
In another embodiment the invention provides compounds represented by formula (I) wherein R3 is a 1H-1,2,3-triazolyl; and wherein the 1H-1,2,3-triazolyl may be optionally substituted on one or more carbon by one or more R10; and wherein the ═N— of the 1H-1,2,3-triazolyl may be optionally substituted by one oxo group; and wherein the —NH— moiety of the 1H-1,2,3-triazolyl may be optionally substituted by a group selected from R11. In one aspect of this embodiment, R10, for each occurrence, is independently selected from the group consisting of methyl, phenyl, trifluoromethyl, and pyridinyl. In another aspect of this embodiment, R11 is benzyl.
In another embodiment the invention provides compounds represented by formula (I) wherein R3 is 1,3-benzothiazolyl; and wherein the 1,3-benzothiazolyl may be optionally substituted on one or more carbon by one or more R10; and wherein the ═N— of the 1,3-benzothiazolyl may be optionally substituted by one oxo group; and wherein the —S— of the 1,3-benzothiazolyl may be optionally substituted by one or two oxo groups. In one aspect of this embodiment, R10 is selected from the group consisting of methyl, phenyl, trifluoromethyl, and pyridinyl.
In another embodiment the invention provides compounds represented by formula (I) wherein R3 is 4-trifluoromethyl-thiazol-2-yl, 4-(pyridin-2-yl)-thiazol-2-yl, 4-phenyl-thiazol-2-yl, 1,3-benzothiazol-2-yl, 2-(pyridin-4-yl)-1,3,4-oxadiazol-5-yl, 1-methyl-1H-pyrazol-5-yl, 1-methyl-1H-pyrazol-4-yl, 2-methyl-1,3,4-oxadiazol-5-yl, or 4-(pyridin-4-yl)-thiazol-2-yl.
In another embodiment the invention provides compounds represented by formula (I) wherein R3 is an aryl which may be optionally substituted on one or more carbon atoms with one or more R10.
In another embodiment the invention provides compounds represented by formula (I) wherein R3 is a morpholinyl wherein the morpholinyl may be optionally substituted on one or more carbon atoms with one or more R10, and wherein the —NH— moiety of the morpholinyl may be optionally substituted by a group selected from R11.
In another embodiment the invention provides compounds represented by formula (I) wherein R3 is a piperidinyl wherein the piperidinyl may be optionally substituted on one or more carbon atoms with one or more R10, and wherein the —NH— moiety of the piperidinyl may be optionally substituted by a group selected from R11.
In one embodiment, R5 is hydrogen.
In another embodiment the invention provides compounds represented by formula (I) wherein R5 is a five membered aromatic heterocyclyl; wherein the heterocyclyl may be optionally substituted on one or more carbon atoms with one or more R14; and wherein if said heterocyclyl contains an ═N— or a —S— moiety that nitrogen may be optionally substituted by one oxo group and that sulfur may be optionally substituted by one or two oxo groups; and wherein if said heterocyclyl contains an —NH— moiety that nitrogen may be optionally substituted by a group selected from R15. In one aspect of this embodiment, R14, for each occurrence, is independently selected from the group consisting of C1-4alkyl and hydroxy. In another aspect of this embodiment, R15 is a C1-4alkyl.
In one embodiment, R5 is a 5-oxo-4,5-dihydro-1,3,4-oxadiazolyl-2-yl wherein the 5-oxo-4,5-dihydro-1,3,4-oxadiazolyl-2-yl may be optionally substituted on one or more carbon atoms with one or more R14; and wherein the ═N— moiety of the 5-oxo-4,5-dihydro-1,3,4-oxadiazolyl-2-yl may be optionally substituted by one oxo group and wherein the —NH— moiety of the 5-oxo-4,5-dihydro-1,3,4-oxadiazolyl-2-yl may be optionally substituted by a group selected from R15. In a particular embodiment, R5 is a 5-oxo-4,5-dihydro-1,3,4-oxadiazolyl-2-yl.
In one embodiment, R5 is a 1,3,4-oxadiazolyl wherein the 1,3,4-oxadiazolyl may be optionally substituted on one or more carbon atoms with one or more R14; and wherein the ═N— moieties of the 1,3,4-oxadiazolyl may be independently optionally substituted by one oxo group. In a particular embodiment, R5 and R14 together are a 5-methyl-1,3,4-oxadiazol-2-yl. In another particular embodiment, R5 and R14 together are selected from 5-isopropyl-1,3,4-oxadiazol-2-yl, 5-amino-1,3,4-oxadiazol-2-yl, a 5-(1-amino-isobutyl)-1,3,4-oxadiazol-2-yl, 5-[3-(N,N-dimethylamino)-propylamino]-1,3,4-oxadiazol-2-yl, 5-morpholino-1,3,4-oxadiazol-2-yl, 5-(morpholin-3-yl)-1,3,4-oxadiazol-2-yl, 5-cyclopropyl-1,3,4-oxadiazol-2-yl, 5-(3-hydroxypiperidino)-1,3,4-oxadiazol-2-yl, 5-(4-hydroxypiperidino)-1,3,4-oxadiazol-2-yl, 5-(3-hydroxyazetidino)-1,3,4-oxadiazol-2-yl, 5-(1-hydroxyethyl)-1,3,4-oxadiazol-2-yl, 5-(1-hydroxyisopropyl)-1,3,4-oxadiazol-2-yl, 5-(1-acetoxyisopropyl)-1,3,4-oxadiazol-2-yl, 542-oxo-propyl)-1,3,4-oxadiazol-2-yl, 5-benzyloxymethyl-1,3,4-oxadiazol-2-yl, 5-(N,N-diethylamino)-1,3,4-oxadiazol-2-yl, 5-(N,N-dimethylaminomethyl)-1,3,4-oxadiazol-2-yl, 5-(methoxymethyl)-1,3,4-oxadiazol-2-yl, 5-ethoxy-1,3,4-oxadiazol-2-yl, 1,3,4-oxadiazol-2-yl, 5-(1-hydroxycyclopropyl)-1,3,4-oxadiazol-2-yl, 5-(N,N-dimethylcarbamoyl)-1,3,4-oxadiazol-2-yl, 5-(2-methoxyethoxymethyl)-1,3,4-oxadiazol-2-yl, 5-(1-amino-1-cyclohexylmethyl)-1,3,4-oxadiazol-2-yl, and 5-(aminomethyl)-1,3,4-oxadiazol-2-yl.
In another embodiment the invention provides compounds represented by formula (I) wherein R5 is selected from the group consisting of 1,3,4-oxadiazolyl, 1,3,4-thiadiazolyl, 1H-tetrazolyl, 1,2,4-oxadiazolyl, 1H-pyrazolyl, 3H-1,2,3,5-oxathiadiazolyl, 1H-imidazolyl, morpholinyl, 4,5-dihydro-oxazolyl, and 1H-1,2,4-triazolyl, wherein the 1,3,4-oxadiazolyl, 1,3,4-thiadiazolyl, 1H-tetrazolyl, 1,2,4-oxadiazolyl, 1H-pyrazolyl, 3H-1,2,3,5-oxathiadiazolyl, 1H-imidazolyl, morpholinyl, 4,5-dihydro-oxazolyl, and 1H-1,2,4-triazolyl may be optionally substituted on one or more carbon atoms with one or more R14; and wherein the ═N— moiety of 1,3,4-oxadiazolyl, 1,3,4-thiadiazolyl, 1H-tetrazolyl, 1,2,4-oxadiazolyl, 1H-pyrazolyl, 3H-1,2,3,5-oxathiadiazolyl, 1H-imidazolyl, 4,5-dihydro-oxazolyl, and 1H-1,2,4-triazolyl may be optionally substituted with one oxo group and the —S— moiety of 1,3,4-thiadiazolyl or 3H-1,2,3,5-oxathiadiazolyl may be optionally substituted by one or two oxo groups; and wherein the —NH— moiety of the 1H-tetrazolyl, 1H-pyrazolyl, 3H-1,2,3,5-oxathiadiazolyl, 1H-imidazolyl, morpholinyl, or the 1H-1,2,4-triazolyl may be optionally substituted by a group selected from R15. In one aspect of this embodiment, R14 is selected from the group consisting of C1-4alkyl or hydroxy. In another aspect of this embodiment, R15 is a C1-4alkyl.
In another embodiment the invention provides compounds represented by formula (I) wherein R5 is selected from the group consisting of 1,3,4-oxadiazolyl, 1,3,4-thiadiazolyl, 1H-tetrazolyl, 1,2,4-oxadiazolyl, 1H-pyrazolyl, 3H-1,2,3,5-oxathiadiazolyl, 1H-imidazolyl, morpholinyl, 4,5-dihydro-oxazolyl, oxazolyl, thiazolyl, and 1H-1,2,4-triazolyl, wherein the 1,3,4-oxadiazolyl, 1,3,4-thiadiazolyl, 1H-tetrazolyl, 1,2,4-oxadiazolyl, 1H-pyrazolyl, 3H-1,2,3,5-oxathiadiazolyl, 1H-imidazolyl, morpholinyl, 4,5-dihydro-oxazolyl, and 1H-1,2,4-triazolyl may be optionally substituted on one or more carbon atoms with one or more R14; and wherein the ═N— moiety of 1,3,4-oxadiazolyl, 1,3,4-thiadiazolyl, 1H-tetrazolyl, 1,2,4-oxadiazolyl, 1H-pyrazolyl, 3H-1,2,3,5-oxathiadiazolyl, 1H-imidazolyl, 4,5-dihydro-oxazolyl, and 1H-1,2,4-triazolyl may be optionally substituted with one oxo group and the —S— moiety of 1,3,4-thiadiazolyl or 3H-1,2,3,5-oxathiadiazolyl may be optionally substituted by one or two oxo groups; and wherein the —NH— moiety of the 1H-tetrazolyl, 1H-pyrazolyl, 3H-1,2,3,5-oxathiadiazolyl, 1H-imidazolyl, morpholinyl, or the 1H-1,2,4-triazolyl may be optionally substituted by a group selected from R15. In one aspect of this embodiment, R14 is selected from the group consisting of C1-4alkyl or hydroxy. In another aspect of this embodiment, R15 is a C1-4alkyl.
In another embodiment the invention provides compounds represented by formula (I) wherein R14 is selected from methyl, isopropyl, amino, trifluoromethyl, difluoromethyl, 1-amino-isobutyl, 3-(N,N-dimethylamino)-propylamino, morpholino, morpholin-3-yl, cyclopropyl, 3-hydroxypiperidino, 4-hydroxypiperidino, 3-hydroxyazetidino, 1-hydroxyethyl, 1-hydroxyisopropyl, 1-acetoxyisopropyl, 2-oxo-propyl, benzyloxymethyl, N,N-diethylamino, N,N-dimethylaminomethyl, methoxymethyl, ethoxy, 1-hydroxycyclopropyl, N,N-dimethylcarbamoyl, 2-methoxyethoxymethyl, 1-amino-1-cyclohexylmethyl, and aminomethyl).
In another embodiment the invention provides compounds represented by formula (I) wherein R15 is selected from methyl, morpholinocarbonyl, and piperidinocarbonyl.
In another embodiment the invention provides compounds represented by formula (I) wherein m is 0.
In another embodiment the invention provides compounds represented by formula (I) wherein m is 0 and X is CH.
In another embodiment the invention provides compounds represented by formula (I) wherein m is 0 and X is N.
In another embodiment the invention provides compounds represented by formula (I) wherein p is 0.
In another embodiment the invention provides compounds represented by formula (I) wherein p is 0 and R5 is hydrogen. In one aspect of this embodiment, ring B is pyridine or quinoxalinyl.
In another embodiment the invention provides compounds represented by formula (I) wherein p is 1. In one aspect of this embodiment, R6 is cyano, bromo, methylsulfonyl, sulphamoyl, or butyloxy.
In another embodiment the invention provides compounds represented by formula (I) wherein p is 1 and R5 is hydrogen. In one aspect of this embodiment, R6 is cyano, bromo, methylsulfonyl, sulphamoyl, or butyloxy.
In another embodiment the invention provides compounds represented by formula (I) wherein p is 2. In one aspect of this embodiment, R6, for each occurrence, is independently selected from cyano, bromo, methylsulfonyl, sulphamoyl, and butyloxy.
In another embodiment the invention provides compounds represented by formula (I) wherein p is 3. In one aspect of this embodiment, R6, for each occurrence, is independently selected from cyano, bromo, methylsulfonyl, sulphamoyl, and butyloxy.
In another embodiment the invention provides compounds represented by formula (I) wherein R6, for each occurrence, is independently selected cyano, fluoro, bromo, ethyl, methylsulfonyl, sulphamoyl, methylsulfonyl, N′ hydroxycarbamimidoyl, carbamimidoyl, pyrrolidinoethoxy, butyloxy, methoxy, ethoxy, isopropoxy, morpholino, cyclopropylmethoxy, N-methylpiperidin-4-yloxy, N-methyl-1H-1,2,4-triazol-5-yl, 5-methyl-1,3,4-oxadiazol-2-yl, pyrimidin-2-yl, N-methyl-piperazin-1-ylethoxy, N-methyl-piperazin-1-ylmethoxy, 2-(N,N-dimethylamino)-ethoxy, 2-morpholinoethoxy, piperidin-4-yloxy, 2-carboxyethoxy, 2H-tetrahydropyran-4-ylmethoxy, 1-methyl-2-(N,N-dimethylamino)-ethoxy, 2-(N,N-diethylamino)-ethoxy, 2-(N,N-diisopropylamino)-ethoxy, 1,2,2,6,6-pentamethyl-piperazin-4-yloxy, 2H-tetrahydropyran-4-yloxy, cyclohexyloxy, cyclopropylmethoxy, cyclopentyloxy, N-isopropylpiperadin-4-yloxy, 3-cyclopentylpropoxy, 2-oxo-propoxy, 2-hydroxy-propoxy, and (1R,3R,5S)-8-methyl-8-azabicyclo[3.2.1]octan-3-yloxy.
In a particular embodiment, the present invention provides compounds having a structural formula (I), or pharmaceutically acceptable salts thereof, as recited above wherein:
In a particular embodiment, the present invention provides compounds having a structural formula (I), or pharmaceutically acceptable salts thereof, as recited above wherein:
In a particular embodiment, the present invention provides compounds having a structural formula (I), or pharmaceutically acceptable salts thereof, as recited above wherein:
In a particular embodiment, the present invention provides compounds having a structural formula (I), or pharmaceutically acceptable salts thereof, as recited above wherein:
In a particular embodiment, the present invention provides compounds having a structural formula (I), or pharmaceutically acceptable salts thereof, as recited above wherein:
In a particular embodiment, the present invention provides compounds having a structural formula (I), or pharmaceutically acceptable salts thereof, as recited above wherein:
Particular compounds of the invention are the compounds of the Examples, and pharmaceutically acceptable salts thereof, each of which provides a further independent aspect of the invention. In further aspects, the present invention also comprises any two or more compounds of the Examples.
In another embodiment, the invention provides pharmaceutical compositions comprising a pharmaceutically acceptable excipient or carrier and a compound represented by formula (I), or a pharmaceutically acceptable salt thereof.
In a further aspect the present invention provides a process for preparing a compound of formula (I), or a pharmaceutically-acceptable salt thereof, wherein variable groups in the schemes below are as defined in formula (I) unless otherwise specified. In general, the compounds of the invention can be prepared by a palladium catalyzed Suzuki coupling reaction of a boronic ester derivative (i) or (iv) and a halo derivative (ii) or (iii), as shown in Schemes I and II. Typically, the coupling reaction is heated and is carried out in the presence of a base such as Cs2CO3.
Boronic ester derivatives can be prepared by heating a halo derivative with a diboron compound such as 4,4,4′,4′,5,5,5′,5′-octamethyl-2,2′-bi(1,3,2-dioxaborolane) in the presence of 1,1′-bis(diphenylphosphino)ferrocene-palladium dichloride in an organic solvent.
The urea portion of the compounds of the invention can be prepared from an isocyanate derivative and an amine derivative either before or after the Suzuki coupling reaction (as shown in Schemes I and II). If the Suzuki coupling reaction is preformed before formation of the urea, the amine is protected with an amine protecting group. When forming the urea derivative, the isocyanate derivative (vi) is typically combined with the amine derivative (v) in an organic solvent and heated, as shown in Scheme III. The solvent can be aqueous, organic or a mixture of an aqueous miscible organic solvent and water.
When R3 is an aryl or a heteroaryl, a Suzuki coupling reaction can be used to attach it to the pyridinyl or pyrimidinyl center ring as shown in Scheme IV. Although Scheme IV shows the coupling reaction of R3 occurring before the coupling reaction to attach ring B, the reactions could be preformed in the alternative order. When the R3 group is attached before the coupling reaction to attach ring B, the center ring the ring can be brominated by heating it with 1-bromopyrrolidine-2,5-dione to form a substrate for the Suzuki coupling reaction shown in Scheme II.
In general, when R5 is a heteroaryl, it can be added by a Suzuki coupling reaction analogous to that shown for R3. Likewise, R5 can be coupled to ring B either before or after ring B is coupled to the pyridinyl or pyrimidinyl center ring.
Alternatively, when R3 or R5 is a heterocyclyl, it can be prepared from an ester derivative either before or after coupling of ring B to the pyridinyl or pyrimidinyl center ring. For example, when R3 is a thiazolyl group, an ester derivative (xiii) can be converted to an amide (xiv) by treating it with a solution of ammonia in an alcohol. The amide derivative (xiv) can then be converted to a thioamide (xv) by treating the amide with Lawessons reagent. The thioamide (xv) is then heated with an α-halo-ketone or an α-halo-aldehyde (xvi) followed by treatment with an acid such as trifluoroacetic acid to form the thiazole (xvii) (see Scheme V). Although the thiazole ring is prepared before the Suzuki coupling reaction to attach ring B in Scheme V, it could also be prepared after the coupling reaction from the ester derivative. When R5 is a thiazolyl group, it can be prepared in an analogous manner either before or after coupling of ring B.
When R3 or R5 is tetrazolyl, it can be prepared by heating a cyano derivative with sodium azide and ammonium chloride in a solvent as shown in Scheme VI for an R5 tetrazolyl group. When R3 is a tetrazolyl group it can be prepared in an analogous manner to that shown in Scheme VI. In addition R3 or R5 tetrazolyl groups can be prepared by the reaction shown in Scheme VI either before or after coupling of ring B to the pyridinyl or pyrimidinyl center ring.
When R3 or R5 is a 1,3,4-oxadiazolyl group, it can be prepared from an ester derivative (xx) by treating the ester with a base in to form a carboxylic acid (xxi). The carboxylic acid (xxi) is then coupled to a hydrazide derivative (xxii) in the presence of the amide coupling reagent HATU to form a dihydrazide derivative (xxiii). The dihydrazide (xxiii) is then treated with triphenyl phosphine in an aprotic organic solvent in the presence of an excess amount of an aprotic base to form a compound of the invention in which the R5 group is 1,3,4-oxadiazolyl (xxiv) as shown in Scheme VII. When R3 is a 1,3,4-oxadiazolyl group it can be prepared in an analogous manner to that shown in Scheme VII. In addition R3 or R5 1,3,4-oxadiazolyl groups can be prepared by the reaction shown in Scheme VII either before or after coupling of ring B to the pyridinyl or pyrimidinyl center ring.
When R3 or R5 is a 1,3,4-thiadiazolyl group, it can be prepared from a dihydrazide derivative (xxiii) (see Scheme VII for preparation of dihydrazide derivatives). The dihydrazide derivative (xxiii) is heated with phosphorous pentasulfide and hexamethyldisiloxane in an organic solvent to form a compound of the invention having an R5 1,3,4-thiadiazolyl group (xxv) as shown in Scheme VIII. When R3 is a 1,3,4-thiadiazolyl group it can be prepared in an analogous manner to that shown in Scheme VIII. In addition R3 or R5 1,3,4-thiadiazolyl groups can be prepared by the reaction shown in Scheme VIII either before or after coupling of ring B to the pyridinyl or pyrimidinyl center ring.
When R3 or R5 is a 5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl group, it can be prepared from a carboxylic acid (xxi) or an ester (x) (see Scheme VII for preparation of the carboxylic acid derivative). The carboxylic acid (xxi) or ester (x) derivative is heated with hydrazine hydrate in an alcohol to form a hydrazide derivative (xxvi). The hydrazide derivative (xxvi) is then reacted with carbonyl diimidazole (xxvii) in the presence of an aprotic base in an aprotic solvent to form a compound of the invention which has an R5 is 5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl (xxviii) as shown in Scheme IX. When R3 is a 5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl group it can be prepared in an analogous manner to that shown in Scheme IX. In addition, R3 or R55-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl groups can be prepared by the reaction shown in Scheme IX either before or after coupling of ring B to the pyridinyl or pyrimidinyl center ring.
When R3 or R5 is a 1,2,4-triazolyl group, it can be prepared from an amide derivative (xxix) by heating it in 1-(N,N-dimethylamino)-1,1-dimethoxy-ethane (xxx) to form (xxxi) (xxxi) is then heated with acetohydrazide in acetic acid to form a compound of the invention that has an R5 1,2,4-triazolyl group (xxxii) as shown in Scheme X. When R3 is a 1,2,4-triazolyl group it can be prepared in an analogous manner to that shown in Scheme X. In addition, R3 or R5 1,2,4-triazolyl groups can be prepared by the reaction shown in Scheme X either before or after coupling of ring B to the pyridinyl or pyrimidinyl center ring.
When R3 or R5 is a 1,2,4-oxadiazolyl group, it can be prepared from (xxxi) by heating (xxxi) with hydroxylamine hydrochloride in a solution of sodium hydroxide in 70% acetic acid in dioxane to form a compound of the invention in which R5 is a 1,2,4-oxadiazolyl group (xxxiii) as shown in Scheme X. When R3 is a 1,2,4-oxadiazolyl group it can be prepared in an analogous manner to that shown in Scheme X. In addition, R3 or R5 1,2,4-oxadiazolyl groups can be prepared by the reaction shown in Scheme X either before or after coupling of ring B to the pyridinyl or pyrimidinyl center ring.
When R3 or R5 is an imidazolyl group, it can be prepared from a cyano derivative (xvii) by stirring the cyano derivative (xvii) at room temperature in a solution of sodium methoxide in methanol for several hours. 1,1-Dimethoxy-2-aminoethane (xxxiv) is then added to the solution and it is heated to give a compound of the invention in which R5 is an imidazolyl group (xxxv) as shown in Scheme XI. When R3 is an imidazolyl group it can be prepared in an analogous manner to that shown in Scheme XI. In addition, R3 or R5 imidazolyl groups can be prepared by the reaction shown in Scheme XI either before or after coupling of ring B to the pyridinyl or pyrimidinyl center ring.
The formation of a pharmaceutically-acceptable salt is within the skill of an ordinary organic chemist using standard techniques.
It will be appreciated that certain of the various ring substituents in the compounds of the present invention may be introduced by standard aromatic substitution reactions or generated by conventional functional group modifications either prior to or immediately following the processes mentioned above, and as such are included in the process aspect of the invention. The reagents used to introduce such ring substituents are either commercially available or are made by processes known in the art.
Introduction of substituents into a ring may convert one compound of the formula (I) into another compound of the formula (I). Such reactions and modifications include, for example, introduction of a substituent by means of an aromatic substitution reaction, reduction of substituents, alkylation of substituents, oxidation of substituents, esterification of substituents, amidation of substituents, formation of heteroaryl rings. The reagents and reaction conditions for such procedures are well known in the chemical art. Particular examples of aromatic substitution reactions include the introduction of alkoxides, diazotization reactions followed by introduction of thiol group, alcohol group, halogen group. Examples of modifications include; oxidation of alkylthio to alkylsulphinyl or alkylsulphonyl.
The skilled organic chemist will be able to use and adapt the information contained and referenced within the above references, and accompanying Examples therein and also the Examples herein, to obtain necessary starting materials, and products. If not commercially available, the necessary starting materials for the procedures such as those described above may be made by procedures which are selected from standard organic chemical techniques, techniques which are analogous to the synthesis of known, structurally similar compounds, or techniques which are analogous to the above described procedure or the procedures described in the examples. It is noted that many of the starting materials for synthetic methods as described above are commercially available and/or widely reported in the scientific literature, or could be made from commercially available compounds using adaptations of processes reported in the scientific literature. The reader is further referred to Advanced Organic Chemistry, 4th Edition, by Jerry March, published by John Wiley & Sons 1992, for general guidance on reaction conditions and reagents.
It will also be appreciated that in some of the reactions mentioned herein it may be necessary/desirable to protect any sensitive groups in compounds. The instances where protection is necessary or desirable are known to those skilled in the art, as are suitable methods for such protection. Conventional protecting groups may be used in accordance with standard practice (for illustration see T. W. Greene, Protective Groups in Organic Synthesis, John Wiley and Sons, 1991).
Examples of a suitable protecting group for a hydroxy group is, for example, an acyl group, for example an alkanoyl group such as acetyl, an aroyl group, for example benzoyl, a silyl group such as trimethylsilyl or an arylmethyl group, for example benzyl. The deprotection conditions for the above protecting groups will necessarily vary with the choice of protecting group. Thus, for example, an acyl group such as an alkanoyl or an aroyl group may be removed, for example, by hydrolysis with a suitable base such as an alkali metal hydroxide, for example lithium or sodium hydroxide. Alternatively a silyl group such as trimethylsilyl may be removed, for example, by fluoride or by aqueous acid; or an arylmethyl group such as a benzyl group may be removed, for example, by hydrogenation in the presence of a catalyst such as palladium-on-carbon.
A suitable protecting group for an amino group is, for example, an acyl group, for example an alkanoyl group such as acetyl, an alkoxycarbonyl group, for example a methoxycarbonyl, ethoxycarbonyl or t-butoxycarbonyl group, an arylmethoxycarbonyl group, for example benzyloxycarbonyl, or an aroyl group, for example benzoyl. The deprotection conditions for the above protecting groups necessarily vary with the choice of protecting group. Thus, for example, an acyl group such as an alkanoyl or alkoxycarbonyl group or an aroyl group may be removed for example, by hydrolysis with a suitable base such as an alkali metal hydroxide, for example lithium or sodium hydroxide. Alternatively an acyl group such as a t-butoxycarbonyl group may be removed, for example, by treatment with a suitable acid as hydrochloric, sulphuric or phosphoric acid or trifluoroacetic acid and an arylmethoxycarbonyl group such as a benzyloxycarbonyl group may be removed, for example, by hydrogenation over a catalyst such as palladium-on-carbon, or by treatment with a Lewis acid for example boron tris(trifluoroacetate). A suitable alternative protecting group for a primary amino group is, for example, a phthaloyl group which may be removed by treatment with an alkylamine, for example dimethylaminopropylamine or 2-hydroxyethylamine, or with hydrazine.
A suitable protecting group for a carboxy group is, for example, an esterifying group, for example a methyl or an ethyl group which may be removed, for example, by hydrolysis with a base such as sodium hydroxide, or for example a t-butyl group which may be removed, for example, by treatment with an acid, for example an organic acid such as trifluoroacetic acid, or for example a benzyl group which may be removed, for example, by hydrogenation over a catalyst such as palladium-on-carbon, or for example, an allyl group which may be removed, for example, by use of a palladium catalyst such as palladium acetate.
The protecting groups may be removed at any convenient stage in the synthesis using conventional techniques well known in the chemical art, or they may be removed during a later reaction step or work-up.
When an optically active form of a compound of the invention is required, it may be obtained by carrying out one of the above procedures using an optically active starting material (formed, for example, by asymmetric induction of a suitable reaction step), or by resolution of a racemic form of the compound or intermediate using a standard procedure, or by chromatographic separation of diastereoisomers (when produced). Enzymatic techniques may also be useful for the preparation of optically active compounds and/or intermediates.
Similarly, when a pure regioisomer of a compound of the invention is required, it may be obtained by carrying out one of the above procedures using a pure regioisomer as a starting material, or by resolution of a mixture of the regioisomers or intermediates using a standard procedure.
Compounds were tested for inhibition of GyrB ATPase activity using an ammonium molybdate/malachite green-based phosphate detection assay (Lanzetta, P. A., L. J. Alvarez, P. S. Reinach, and O. A. Candia, 1979, 100: 95-97). Assays were performed in multiwell plates in 100 μl reactions containing: 50 mM TRIS buffer pH 7.5, 75 mM ammonium acetate, 5.5 mM magnesium chloride, 0.5 mM ethylenediaminetetraacetic acid, 5% glycerol, 1 mM 1,4-Dithio-DL-threitol, 200 nM bovine serum albumin, 16 μg/ml sheared salmon sperm DNA, 4 nM E. coli GyrA, 4 nM E. coli GyrB, 250 μM ATP, and compound in dimethylsulfoxide. Reactions were quenched with 150 μl of ammonium molybdate/malachite green detection reagent containing 1.2 mM malachite green hydrochloride, 8.5 mM ammonium molybdate tetrahydrate, and 1 M hydrochloric acid. Plates were read in an absorbance plate reader at 625 nm and percent inhibition values were calculated using dimethylsulfoxide (2%)-containing reactions as 0% inhibition and novobiocin-containing (2 μM) reactions as 100% inhibition controls. Compound potency was based on IC50 measurements determined from reactions performed in the presence of 10 different compound concentrations.
Compounds were tested for inhibition of topoisomerase IV ATPase activity as described above for GyrB except the 100 μl reactions contained the following: 20 mM TRIS buffer pH 8, 50 mM ammonium acetate, 8 mM magnesium chloride, 5% glycerol, 5 mM 1,4-Dithio-DL-threitol, 0.005% Brij-35, 5 μg/ml sheared salmon sperm DNA, 10 nM E. coli ParC, 10 nM E. coli ParE, 160 μM ATP, and compound in dimethylsulfoxide. Compound potency was based on IC50 measurements determined from reactions performed in the presence of 10 different compound concentrations.
Compounds of the invention generally have IC50 values of <200 μg/ml in one or both assays described herein above.
Compounds were tested for inhibition of GyrB ATPase activity using an ammonium molybdate/malachite green-based phosphate detection assay (Lanzetta, P. A., L. J. Alvarez, P. S. Reinach, and O. A. Candia, 1979, 100: 95-97). Assays were performed in multiwell plates in 100 μl reactions containing: 50 mM Hepes buffer pH 7.5, 75 mM ammonium acetate, 8.0 mM magnesium chloride, 1.0 mM ethylenediaminetetraacetic acid, 5% glycerol, 2 mM 1,4-Dithio-DL-threitol, 400 nM bovine serum albumin, 5 μg/ml sheared salmon sperm DNA, 1.25 nM E. coli GyrA, 1.25 nM S. aureus GyrB, 500 μM ATP, and compound in dimethylsulfoxide. Reactions were quenched with 150 μl of ammonium molybdate/malachite green detection reagent containing 1.2 mM malachite green hydrochloride, 8.5 mM ammonium molybdate tetrahydrate, and 1 M hydrochloric acid. Plates were read in an absorbance plate reader at 650 nm and percent inhibition values were calculated using dimethylsulfoxide (2%)-containing reactions as 0% inhibition and novobiocin-containing (2 μM) reactions as 100% inhibition controls. Compound potency was based on IC50 measurements determined from reactions performed in the presence of 10 different compound concentrations.
Table 1 shows S. aureus (SAU) GyrB ATPase IC50 values for representative compounds of the invention.
Table 2 shows S. aureus (SAU) GyrB ATPase percent inhibition for compounds of the invention at a compound concentration of 1.0 μM unless otherwise noted. Where the assay was carried out more than one time for a particular compound of the invention, the percent inhibition shown in Table 2 is an average value.
Compounds were tested for antimicrobial activity by susceptibility testing in liquid media. Compounds were dissolved in dimethylsulfoxide and tested in 10 doubling dilutions in the susceptibility assays. The organisms used in the assay were grown overnight on suitable agar media and then suspended in a liquid medium appropriate for the growth of the organism. The suspension was a 0.5 McFarland and a further 1 in 10 dilution was made into the same liquid medium to prepare the final organism suspension in 100 μL. Plates were incubated under appropriate conditions at 37° C. for 24 hrs prior to reading. The Minimum Inhibitory Concentration was determined as the lowest drug concentration able to reduce growth by 80% or more.
Example 14 had an MIC of 0.39 uM against Streptococcus pneumoniae.
According to a further feature of the invention there is provided a compound of the formula (I), or a pharmaceutically-acceptable salt thereof, for use in a method of treatment of the human or animal body by therapy.
In one embodiment, the invention provides a method of treating a bacterial infection in an animal, such as a human, comprising administering to the animal or human an effective amount of a compound of any one of formulas (I), or a pharmaceutically acceptable salt thereof.
We have found that compounds of the present invention inhibit bacterial DNA gyrase and/or topoisomerase IV and are therefore of interest for their antibacterial effects. In one aspect of the invention the compounds of the invention inhibit bacterial DNA gyrase and are therefore of interest for their antibacterial effects. In one aspect of the invention, the compounds of the invention inhibit topoisomerase IV and are therefore of interest for their antibacterial effects. In one aspect of the invention, the compounds of the invention inhibit both DNA gyrase and topoisomerase IV and are therefore of interest for their antibacterial effects. Thus, the compounds of the invention are useful in treating or preventing bacterial infections.
In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Acinetobacter baumanii. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Acinetobacter haemolyticus. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Acinetobacter junii. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Acinetobacter johnsonii. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Acinetobacter lwoffi. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Bacteroides bivius. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Bacteroides fragilis. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Burkholderia cepacia. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Campylobacter jejuni. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Chlamydia pneumoniae. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Chlamydia urealyticus. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Chlamydophila pneumoniae. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Clostridium difficile. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Enterobacter aerogenes. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Enterobacter cloacae. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Enterococcus faecalis. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Enterococcus faecium. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Escherichia coli. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Gardnerella vaginalis. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Haemophilus parainfluenzae. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Haemophilus influenzae. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Helicobacter pylori. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Klebsiella pneumoniae. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Legionella pneumophila. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Methicillin-resistant Staphylococcus aureus. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Methicillin-susceptible Staphylococcus aureus. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Moraxella catarrhalis. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Morganella morganii. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Mycoplasma pneumoniae. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Neisseria gonorrhoeae. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Penicillin-resistant Streptococcus pneumoniae. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Penicillin-susceptible Streptococcus pneumoniae. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Peptostreptococcus magnus. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Peptostreptococcus micros. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Peptostreptococcus anaerobius. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Peptostreptococcus asaccharolyticus. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Peptostreptococcus prevotii. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Peptostreptococcus tetradius. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Peptostreptococcus vaginalis. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Proteus mirabilis. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Pseudomonas aeruginosa. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Quinolone-Resistant Staphylococcus aureus. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Quinolone-Resistant Staphylococcus epidermis. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Salmonella typhi. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Salmonella paratyphi. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Salmonella enteritidis. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Salmonella typhimurium. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Serratia marcescens. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Staphylococcus aureus. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Staphylococcus epidermidis. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Staphylococcus saprophyticus. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Streptoccocus agalactiae. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Streptococcus pneumoniae. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Streptococcus pyogenes. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Stenotrophomonas maltophilia. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Ureaplasma urealyticum. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Vancomycin-Resistant Enterococcus faecium. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Vancomycin-Resistant Enterococcus faecalis. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Vancomycin-Resistant Staphylococcus aureus. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Vancomycin-Resistant Staphylococcus epidermis. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Mycobacterium tuberculosis. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Clostridium perfringens. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Klebsiella oxytoca. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Neisseria miningitidis. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Fusobacterium spp. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Peptococcus spp. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Proteus vulgaris. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Coagulase-negative Staphylococcus (including Staphylococcus lugdunensis, Staphylococcus capitis, Staphylococcus hominis, and Staphylococcus saprophyticus).
In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Acinetobacter spp. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Bacteroides spp. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Burkholderia spp. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Campylobacter spp. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Chlamydia spp. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Chlamydophila spp. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Clostridium spp. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Enterobacter spp. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Enterococcus spp. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Escherichia spp. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Gardnerella spp. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Haemophilus spp. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Helicobacter spp. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Klebsiella spp. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Legionella spp. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Moraxella spp. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Morganella spp. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Mycoplasma spp. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Neisseria spp. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Peptostreptococcus spp. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Proteus spp. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Pseudomonas spp. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Salmonella spp. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Serratia spp. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Staphylococcus spp. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Streptoccocus spp. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Stenotrophomonas spp. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Ureaplasma spp. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by aerobes. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by obligate anaerobes. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by facultative anaerobes. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by gram-positive bacteria. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by gram-negative bacteria. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by gram-variable bacteria. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by atypical respiratory pathogens. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Enterics. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Shigella spp. In one aspect of the invention an “infection” or “bacterial infection” refers to an infection caused by Citrobacter.
In one aspect of the invention “infection” or “bacterial infection” refers to a gynecological infection. In one aspect of the invention “infection” or “bacterial infection” refers to a respiratory tract infection (RTI). In one aspect of the invention “infection” or “bacterial infection” refers to a sexually transmitted disease. In one aspect of the invention “infection” or “bacterial infection” refers to a urinary tract infection. In one aspect of the invention “infection” or “bacterial infection” refers to acute exacerbation of chronic bronchitis (ACEB). In one aspect of the invention “infection” or “bacterial infection” refers to acute otitis media. In one aspect of the invention “infection” or “bacterial infection” refers to acute sinusitis. In one aspect of the invention “infection” or “bacterial infection” refers to an infection caused by drug resistant bacteria. In one aspect of the invention “infection” or “bacterial infection” refers to catheter-related sepsis. In one aspect of the invention “infection” or “bacterial infection” refers to chancroid. In one aspect of the invention “infection” or “bacterial infection” refers to chlamydia. In one aspect of the invention “infection” or “bacterial infection” refers to community-acquired pneumonia (CAP). In one aspect of the invention “infection” or “bacterial infection” refers to complicated skin and skin structure infection. In one aspect of the invention “infection” or “bacterial infection” refers to uncomplicated skin and skin structure infection. In one aspect of the invention “infection” or “bacterial infection” refers to endocarditis. In one aspect of the invention “infection” or “bacterial infection” refers to febrile neutropenia. In one aspect of the invention “infection” or “bacterial infection” refers to gonococcal cervicitis. In one aspect of the invention “infection” or “bacterial infection” refers to gonococcal urethritis. In one aspect of the invention “infection” or “bacterial infection” refers to hospital-acquired pneumonia (HAP). In one aspect of the invention “infection” or “bacterial infection” refers to osteomyelitis. In one aspect of the invention “infection” or “bacterial infection” refers to sepsis. In one aspect of the invention “infection” or “bacterial infection” refers to syphilis. In one aspect of the invention “infection” or “bacterial infection” refers to ventilator-associated pneumonia. In one aspect of the invention “infection” or “bacterial infection” refers to intraabdominal infections. In one aspect of the invention “infection” or “bacterial infection” refers to gonorrhoeae. In one aspect of the invention “infection” or “bacterial infection” refers to meningitis. In one aspect of the invention “infection” or “bacterial infection” refers to tetanus. In one aspect of the invention “infection” or “bacterial infection” refers to tuberculosis.
In one embodiment, it is expected that the compounds of the present invention will be useful in treating bacterial infections including, but not limited to community-acquired pneumoniae, hospital-acquired pneumoniae, skin & skin structure infections, acute exacerbation of chronic bronchitis, acute sinusitis, acute otitis media, catheter-related sepsis, febrile neutropenia, osteomyelitis, endocarditis, urinary tract infections and infections caused by drug resistant bacteria such as Penicillin-resistant Streptococcus pneumoniae, methicillin-resistant Staphylococcus aureus, methicillin-resistant Staphylococcus epidermidis and Vancomycin-Resistant Enterococci.
According to a further feature of the present invention there is provided a method for producing an antibacterial effect in a warm blooded animal, such as man, in need of such treatment, which comprises administering to said animal an effective amount of a compound of the present invention, or a pharmaceutically-acceptable salt thereof.
According to a further feature of the invention there is provided a method for inhibition of bacterial DNA gyrase and/or topoisomerase IV in a warm-blooded animal, such as a human being, in need of such treatment which comprises administering to said animal an effective amount of a compound of formula (I), or a pharmaceutically acceptable salt thereof as defined hereinbefore.
According to a further feature of the invention there is provided a method of treating a bacterial infection in a warm-blooded animal, such as a human being, in need of such treatment which comprises administering to said animal an effective amount of a compound of formula (I), or a pharmaceutically acceptable salt thereof as defined hereinbefore.
According to a further feature of the invention there is provided a method of treating a bacterial infection selected from community-acquired pneumoniae, hospital-acquired pneumoniae, skin & skin structure infections, acute exacerbation of chronic bronchitis, acute sinusitis, acute otitis media, catheter-related sepsis, febrile neutropenia, osteomyelitis, endocarditis, urinary tract infections and infections caused by drug resistant bacteria such as Penicillin-resistant Streptococcus pneumoniae, methicillin-resistant Staphylococcus aureus, methicillin-resistant Staphylococcus epidermidis and Vancomycin-Resistant Enterococciin a warm-blooded animal, such as a human being, in need of such treatment which comprises administering to said animal an effective amount of a compound of formula (I), or a pharmaceutically acceptable salt thereof as defined hereinbefore.
A further feature of the present invention is a compound of formula (I), and pharmaceutically acceptable salts thereof for use as a medicament. Suitably the medicament is an antibacterial agent.
According to a further aspect of the invention there is provided the use of a compound of formula (I), or a pharmaceutically acceptable salt thereof in the manufacture of a medicament for use in the production of an anti-bacterial effect in a warm-blooded animal such as a human being.
According to a further aspect of the invention there is provided the use of a compound of formula (I), or a pharmaceutically acceptable salt thereof, in the manufacture of a medicament for use in inhibition of bacterial DNA gyrase and/or topoisomerase IV in a warm-blooded animal such as a human being.
Thus according to a further aspect of the invention there is provided the use of a compound of formula (I), or a pharmaceutically acceptable salt thereof, in the manufacture of a medicament for use in the treatment of a bacterial infection in a warm-blooded animal such as a human being.
Thus according to a further aspect of the invention there is provided the use of a compound of formula (I), or a pharmaceutically acceptable salt thereof, in the manufacture of a medicament for use in the treatment of a bacterial infection selected from community-acquired pneumoniae, hospital-acquired pneumoniae, skin & skin structure infections, acute exacerbation of chronic bronchitis, acute sinusitis, acute otitis media, catheter-related sepsis, febrile neutropenia, osteomyelitis, endocarditis, urinary tract infections and infections caused by drug resistant bacteria such as Penicillin-resistant Streptococcus pneumoniae, methicillin-resistant Staphylococcus aureus, methicillin-resistant Staphylococcus epidermidis and Vancomycin-Resistant Enterococci in a warm-blooded animal such as a human being.
According to a further aspect of the invention there is provided a compound of formula (I), or a pharmaceutically acceptable salt thereof, for use in the production of an anti-bacterial effect in a warm-blooded animal such as a human being.
According to a further aspect of the invention there is provided a compound of formula (I), or a pharmaceutically acceptable salt thereof, for use in inhibition of bacterial DNA gyrase and/or topoisomerase IV in a warm-blooded animal such as a human being.
Thus according to a further aspect of the invention there is provided a compound of formula (I), or a pharmaceutically acceptable salt thereof, for use in the treatment of a bacterial infection in a warm-blooded animal such as a human being.
Thus according to a further aspect of the invention there is provided a compound of formula (I), or a pharmaceutically acceptable salt thereof, for use in the treatment of a bacterial infection selected from community-acquired pneumoniae, hospital-acquired pneumoniae, skin & skin structure infections, acute exacerbation of chronic bronchitis, acute sinusitis, acute otitis media, catheter-related sepsis, febrile neutropenia, osteomyelitis, endocarditis, urinary tract infections and infections caused by drug resistant bacteria such as Penicillin-resistant Streptococcus pneumoniae, methicillin-resistant Staphylococcus aureus, methicillin-resistant Staphylococcus epidermidis and Vancomycin-Resistant Enterococci in a warm-blooded animal such as a human being.
In order to use a compound of the formula (I), or a pharmaceutically-acceptable salt thereof, (hereinafter in this section relating to pharmaceutical composition “a compound of this invention”) for the therapeutic (including prophylactic) treatment of mammals including humans, in particular in treating infection, it is normally formulated in accordance with standard pharmaceutical practice as a pharmaceutical composition.
Therefore in another aspect the present invention provides a pharmaceutical composition which comprises a compound of the formula (I), or a pharmaceutically-acceptable salt thereof, and a pharmaceutically-acceptable diluent or carrier.
According to a further aspect of the invention there is provided a pharmaceutical composition which comprises a compound of formula (I), as defined hereinbefore or a pharmaceutically acceptable salt thereof, in association with a pharmaceutically acceptable excipient or carrier for use in producing an anti-bacterial effect in an warm-blooded animal, such as a human being.
According to a further aspect of the invention there is provided a pharmaceutical composition which comprises a compound of formula (I), as defined hereinbefore or a pharmaceutically acceptable salt thereof, in association with a pharmaceutically acceptable excipient or carrier for use in inhibition of bacterial DNA gyrase and/or topoisomerase IV in an warm-blooded animal, such as a human being.
According to a further aspect of the invention there is provided a pharmaceutical composition which comprises a compound of formula (I), as defined hereinbefore or a pharmaceutically acceptable salt thereof, in association with a pharmaceutically acceptable excipient or carrier for use in the treatment of a bacterial infection in an warm-blooded animal, such as a human being.
According to a further aspect of the invention there is provided a pharmaceutical composition which comprises a compound of formula (I), as defined hereinbefore or a pharmaceutically acceptable salt thereof, in association with a pharmaceutically acceptable excipient or carrier for use in the treatment of a bacterial infection selected from community-acquired pneumoniae, hospital-acquired pneumoniae, skin & skin structure infections, acute exacerbation of chronic bronchitis, acute sinusitis, acute otitis media, catheter-related sepsis, febrile neutropenia, osteomyelitis, endocarditis, urinary tract infections and infections caused by drug resistant bacteria such as Penicillin-resistant Streptococcus pneumoniae, methicillin-resistant Staphylococcus aureus, methicillin-resistant Staphylococcus epidermidis and Vancomycin-Resistant Enterococci in an warm-blooded animal, such as a human being.
The compositions of the invention may be in a form suitable for oral use (for example as tablets, lozenges, hard or soft capsules, aqueous or oily suspensions, emulsions, dispersible powders or granules, syrups or elixirs), for topical use (for example as creams, ointments, gels, or aqueous or oily solutions or suspensions), for administration by inhalation (for example as a finely divided powder or a liquid aerosol), for administration by insufflation (for example as a finely divided powder) or for parenteral administration (for example as a sterile aqueous or oily solution for intravenous, subcutaneous, intramuscular or intramuscular dosing or as a suppository for rectal dosing).
The compositions of the invention may be obtained by conventional procedures using conventional pharmaceutical excipients, well known in the art. Thus, compositions intended for oral use may contain, for example, one or more colouring, sweetening, flavouring and/or preservative agents.
Suitable pharmaceutically acceptable excipients for a tablet formulation include, for example, inert diluents such as lactose, sodium carbonate, calcium phosphate or calcium carbonate, granulating and disintegrating agents such as corn starch or algenic acid; binding agents such as starch; lubricating agents such as magnesium stearate, stearic acid or talc; preservative agents such as ethyl or propyl p-hydroxybenzoate, and anti-oxidants, such as ascorbic acid. Tablet formulations may be uncoated or coated either to modify their disintegration and the subsequent absorption of the active ingredient within the gastrointestinal tract, or to improve their stability and/or appearance, in either case, using conventional coating agents and procedures well known in the art.
Compositions for oral use may be in the form of hard gelatin capsules in which the active ingredient is mixed with an inert solid diluent, for example, calcium carbonate, calcium phosphate or kaolin, or as soft gelatin capsules in which the active ingredient is mixed with water or an oil such as peanut oil, liquid paraffin, or olive oil.
Aqueous suspensions generally contain the active ingredient in finely powdered form together with one or more suspending agents, such as sodium carboxymethylcellulose, methylcellulose, hydroxypropylmethylcellulose, sodium alginate, polyvinyl-pyrrolidone, gum tragacanth and gum acacia; dispersing or wetting agents such as lecithin or condensation products of an alkylene oxide with fatty acids (for example polyoxethylene stearate), or condensation products of ethylene oxide with long chain aliphatic alcohols, for example heptadecaethyleneoxycetanol, or condensation products of ethylene oxide with partial esters derived from fatty acids and a hexitol such as polyoxyethylene sorbitol monooleate, or condensation products of ethylene oxide with long chain aliphatic alcohols, for example heptadecaethyleneoxycetanol, or condensation products of ethylene oxide with partial esters derived from fatty acids and a hexitol such as polyoxyethylene sorbitol monooleate, or condensation products of ethylene oxide with partial esters derived from fatty acids and hexitol anhydrides, for example polyethylene sorbitan monooleate. The aqueous suspensions may also contain one or more preservatives (such as ethyl or propyl p-hydroxybenzoate, anti-oxidants (such as ascorbic acid), colouring agents, flavouring agents, and/or sweetening agents (such as sucrose, saccharine or aspartame).
Oily suspensions may be formulated by suspending the active ingredient in a vegetable oil (such as arachis oil, olive oil, sesame oil or coconut oil) or in a mineral oil (such as liquid paraffin). The oily suspensions may also contain a thickening agent such as beeswax, hard paraffin or cetyl alcohol. Sweetening agents such as those set out above, and flavouring agents may be added to provide a palatable oral preparation. These compositions may be preserved by the addition of an anti-oxidant such as ascorbic acid.
Dispersible powders and granules suitable for preparation of an aqueous suspension by the addition of water generally contain the active ingredient together with a dispersing or wetting agent, suspending agent and one or more preservatives. Suitable dispersing or wetting agents and suspending agents are exemplified by those already mentioned above. Additional excipients such as sweetening, flavouring and colouring agents, may also be present.
The pharmaceutical compositions of the invention may also be in the form of oil-in-water emulsions. The oily phase may be a vegetable oil, such as olive oil or arachis oil, or a mineral oil, such as for example liquid paraffin or a mixture of any of these. Suitable emulsifying agents may be, for example, naturally-occurring gums such as gum acacia or gum tragacanth, naturally-occurring phosphatides such as soya bean, lecithin, an esters or partial esters derived from fatty acids and hexitol anhydrides (for example sorbitan monooleate) and condensation products of the said partial esters with ethylene oxide such as polyoxyethylene sorbitan monooleate. The emulsions may also contain sweetening, flavouring and preservative agents.
Syrups and elixirs may be formulated with sweetening agents such as glycerol, propylene glycol, sorbitol, aspartame or sucrose, and may also contain a demulcent, preservative, flavouring and/or colouring agent.
The pharmaceutical compositions may also be in the form of a sterile injectable aqueous or oily suspension, which may be formulated according to known procedures using one or more of the appropriate dispersing or wetting agents and suspending agents, which have been mentioned above. A sterile injectable preparation may also be a sterile injectable solution or suspension in a non-toxic parenterally-acceptable diluent or solvent, for example a solution in 1,3-butanediol.
Compositions for administration by inhalation may be in the form of a conventional pressurised aerosol arranged to dispense the active ingredient either as an aerosol containing finely divided solid or liquid droplets. Conventional aerosol propellants such as volatile fluorinated hydrocarbons or hydrocarbons may be used and the aerosol device is conveniently arranged to dispense a metered quantity of active ingredient.
For further information on formulation the reader is referred to Chapter 25.2 in Volume 5 of Comprehensive Medicinal Chemistry (Corwin Hansch; Chairman of Editorial Board), Pergamon Press 1990.
The amount of active ingredient that is combined with one or more excipients to produce a single dosage form will necessarily vary depending upon the host treated and the particular route of administration. For example, a formulation intended for oral administration to humans will generally contain, for example, from 0.5 mg to 2 g of active agent compounded with an appropriate and convenient amount of excipients which may vary from about 5 to about 98 percent by weight of the total composition. Dosage unit forms will generally contain about 1 mg to about 500 mg of an active ingredient. For further information on Routes of Administration and Dosage Regimes the reader is referred to Chapter 25.3 in Volume 5 of Comprehensive Medicinal Chemistry (Corwin Hansch; Chairman of Editorial Board), Pergamon Press 1990.
The compounds of the invention described herein may be applied as a sole therapy or may involve, in addition to a compound of the invention, one or more other substances and/or treatments. Such conjoint treatment may be achieved by way of the simultaneous, sequential or separate administration of the individual components of the treatment. Where the administration is sequential or separate, the delay in administering the second component should not be such as to lose the beneficial effect of the combination. Suitable classes and substances may be selected from one or more of the following:
Therefore, in a further aspect of the invention there is provided a compound of the formula (I), or a pharmaceutically acceptable salt thereof, and a chemotherapeutic agent selected from:
In another embodiment, the invention relates to a method of treating a bacterial infection in an animal, such as a human, comprising administering to the animal an effective amount of a compound of formula (I), or a pharmaceutically acceptable salt thereof, and a chemotherapeutic agent selected from:
As stated above the size of the dose required for the therapeutic or prophylactic treatment of a particular disease state will necessarily be varied depending on the host treated, the route of administration, the severity of the illness being treated, and whether or not an additional chemotherapeutic agent is administered in combination with a compound of the invention. Preferably a daily dose in the range of 1-50 mg/kg is employed. However the daily dose will necessarily be varied depending upon the host treated, the particular route of administration, the severity of the illness being treated, and whether or not an additional chemotherapeutic agent is administered in combination with a compound of the invention. Accordingly the optimum dosage may be determined by the practitioner who is treating any particular patient.
As noted above, one embodiment of the present invention is directed to treating or preventing diseases caused by bacterial infections, wherein the bacteria comprise a GyrB ATPase or topoisomerase IV ATPase enzyme. “Treating a subject with a disease caused by a bacterial infection” includes achieving, partially or substantially, one or more of the following: the reducing or amelioration of the progression, severity and/or duration of the infection, arresting the spread of an infection, ameliorating or improving a clinical symptom or indicator associated with a the infection (such as tissue or serum components), and preventing the reoccurrence of the infection.
As used herein, the terms “preventing a bacterial infection” refer to the reduction in the risk of acquiring the infection, or the reduction or inhibition of the recurrence of the infection. In a preferred embodiment, a compound of the invention is administered as a preventative measure to a patient, preferably a human, before a surgical procedure is preformed on the patient to prevent infection.
As used herein, the term “effective amount” refers to an amount of a compound of this invention for treating or preventing a bacterial infection is an amount which is sufficient to prevent the onset of an infection, reduce or ameliorate the severity, duration, or progression, of an infection, prevent the advancement of an infection, cause the regression of an infection, prevent the recurrence, development, onset or progression of a symptom associated with an infection, or enhance or improve the prophylactic or therapeutic effect(s) of another therapy.
In addition to its use in therapeutic medicine, compounds of formula (I), and their pharmaceutically acceptable salts, are also useful as pharmacological tools in the development and standardization of in-vitro and in-vivo test systems for the evaluation of the effects of inhibitors of DNA gyrase and/or topoisomerase IV in laboratory animals such as cats, dogs, rabbits, monkeys, rats and mice, as part of the search for new therapeutic agents.
In the above other, pharmaceutical composition, process, method, use and medicament manufacture features, the alternative and particular embodiments of the compounds of the invention described herein also apply.
The invention is now illustrated but not limited by the following Examples in which unless otherwise stated:—
(i) evaporations were carried out by rotary evaporation in-vacuo and work-up procedures were carried out after removal of residual solids by filtration;
(ii) operations were generally carried out at ambient temperature, that is typically in the range 18-26° C. and without exclusion of air unless otherwise stated, or unless the skilled person would otherwise work under an inert atmosphere;
(iii) column chromatography (by the flash procedure) was used to purify compounds and was performed on Merck Kieselgel silica (Art. 9385) unless otherwise stated;
(iv) yields are given for illustration only and are not necessarily the maximum attainable; the structure of the end-products of the invention were generally confirmed by NMR and mass spectral techniques; proton magnetic resonance spectra is quoted and was generally determined in DMSO-d6 unless otherwise stated using a Bruker DRX-300 spectrometer operating at a field strength of 300 MHz. Chemical shifts are reported in parts per million downfield from tetramethysilane as an internal standard (δ scale) and peak multiplicities are shown thus: s, singlet; d, doublet; AB or dd, doublet of doublets; dt, doublet of triplets; dm, doublet of multiplets; t, triplet, m, multiplet; br, broad; fast-atom bombardment (FAB) mass spectral data were generally obtained using a Platform spectrometer (supplied by Micromass) run in electrospray and, where appropriate, either positive ion data or negative ion data were collected or using Agilent 1100 series LC/MSD equipped with Sedex 75ELSD, run in atmospheric pressure chemical ionisation mode and, where appropriate, either positive ion data or negative ion data were collected; mass spectra were run with an electron energy of 70 electron volts in the chemical ionization (CI) mode using a direct exposure probe; where indicated ionization was effected by electron impact (EI), fast atom bombardment (FAB) or electrospray (ESP); values for m/z are given; generally, only ions which indicate the parent mass are reported;
(vi) each intermediate was purified to the standard required for the subsequent stage and was characterised in sufficient detail to confirm that the assigned structure was correct; purity was assessed by high pressure liquid chromatography, thin layer chromatography, or NMR and identity was determined by infra-red spectroscopy (IR), mass spectroscopy or NMR spectroscopy as appropriate;
(vii) the following abbreviations may be used:
Triethylamine (0.054 mL, 0.39 mmol) and acetohydrazide (14.40 mg, 0.19 mmol) were added to a solution of 6′-(3-ethylureido)-4′-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridine-5-carboxylic acid (Intermediate 1, 85 mg, 0.19 mmol) in DMF (1.5 mL). The mixture was stirred for 5 minutes and then HATU (89 mg, 0.23 mmol) was added. The resulting light yellow solution was stirred at room temperature for one hour. Then the reaction was diluted with water and the aqueous layer was lyophilized to remove water. The residue obtained was extracted with THF and concentrated to give thick oil. The oil was taken up in DCM (5 mL) and triphenyl phosphine (6 eq, 306 mg, 1.16 mmol), carbon tetrachloride (3 eq, 180 mg, 113 uL, 0.58 mmol), and triethylamine (6 eq, 319 mg, 0.431 uL, 1.16 mmol) were added and allowed to stir overnight at room temperature. The reaction was concentrated and partitioned between water and dichloromethane. The organic layer was washed with water and brine, then dried over magnesium sulfate. The crude residue was purified by normal phase chromatography to give a white solid as the product (48 mg).
MS (ES) MH+: 476 for C20H16F3N7O2S
1H-NMR (DMSO-d6) δ: 1.09 (t, 3H); 2.58 (s, 3H); 3.16-3.24 (m, 2H); 7.54 (brs, 1H); 8.23 (s, 1H); 8.35 (s, 1H); 8.40 (s, 1H); 8.56 (s, 1H); 8.69 (s, 1H); 9.15 (d, 1H); 9.51 (s, 1H).
1-(5-Bromo-4-(4-(trifluoromethyl)thiazol-2-yl)pyridin-2-yl)-3-ethylurea (Intermediate 3, 300 mg, 0.76 mmol), cesium carbonate (495 mg, 1.52 mmol), tetrakis(triphenylphosphine)palladium (0) (88 mg, 0.08 mmol), and 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)nicotinonitrile (349 mg, 1.52 mmol) were taken in a microwave vial and degassed with nitrogen. Then dioxane:water (4:1, 6 mL) was added to the vial and the mixture was microwaved at 100° C. for half an hour. The reaction mixture was partitioned between water and ethyl acetate and the layers were separated. The aqueous layer was back extracted with ethyl acetate (2-3 times). The combined organic layers were washed with saturated sodium bicarbonate solution, water, brine and dried over magnesium sulfate. The solvent was removed and the residue was washed with acetonitrile to give the title compound as a white solid (270 mg).
MS (ESP): 419 (M+1) for C18H13FN6OS
1H-NMR (DMSO-d6) δ: 1.09 (t, 3H); 3.16-3.22 (m, 2H); 7.49 (t, 1H); 8.22 (s, 1H); 8.36 (s, 1H); 8.38 (d, 1H); 8.60 (s, 1H); 8.76 (s, 1H); 9.04 (s, 1H); 9.52 (s, 1H).
Sodium azide (18.65 mg, 0.29 mmol) and ammonium chloride (14.57 mg, 0.27 mmol) were added to a solution of 1-(5′-cyano-4-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridin-6-yl)-3-ethylurea (Example 2, 60 mg, 0.14 mmol) in DMF (1.5 mL), and the mixture was heated at 100° C. for 5-6 hours. The reaction was then concentrated and dissolved in water and methanol (3 mL, 1:1) and purified by reverse phase. Fractions were collected and lyophilized to give the product as a white solid (23 mg).
MS (ESP): 462 (M+1) for C18H14FN9OS
1H-NMR (DMSO-d6: 1.09 (t, 3H); 3.17-3.22 (m, 2H); 7.53 (t, 1H); 8.25 (s, 1H); 8.35 (s, 1H); 8.40 (s, 1H); 8.55 (s, 1H); 8.77 (d, 1H); 9.22 (s, 1H); 9.53 (s, 1H).
Triphenylphosphine (211 mg, 0.81 mmol), carbon tetrachloride (0.039 mL, 0.40 mmol) and triethylamine (0.112 mL, 0.81 mmol) were added to a mixture of 1-ethyl-3-(5′-(2-isobutyrylhydrazinecarbonyl)-4-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridin-6-yl)urea (Intermediate 8, 70 mg, 0.13 mmol) in DCM (4 mL). The resulting mixture was allowed to stir overnight at room temperature, then was partitioned between water and dichloromethane. The layers were separated and the aqueous was back extracted with dichloromethane. The combined extract was washed with water, dried over magnesium sulfate and concentrated. The residue obtained was purified by normal phase (1% MeOH to 5% MeOH in dichloromethane) to give the product as a white solid (23 mg).
MS (ESP): 504 (M+1) for C22H20F3N7O2S
1H-NMR (DMSO-d6) δ: 1.10 (t, 3H); 1.35 (d, 6H); 3.10-3.25 (m, 2H); 3.23-3.30 (m, 1H); 7.55 (brs, 1H); 8.22 (s, 1H); 8.29 (s, 1H); 8.41 (s, 1H); 8.57 (s, 1H); 8.70 (d, 1H); 9.18 (s, 1H); 9.51 (s, 1H).
Phosphorus pentasulfide (79 mg, 0.35 mmol) and hexamethyldisiloxane (0.030 mL, 0.14 mmol) were added to a mixture of 1-ethyl-3-(5′-(2-isobutyrylhydrazinecarbonyl)-4-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridin-6-yl)urea (Intermediate 8, 70 mg, 0.14 mmol) in toluene, and the mixture was refluxed overnight. The reaction was cooled to the room temperature and diluted with acetone (5 mL) and potassium carbonate (31.4 mg, 0.23 mmol) was added slowly. After the completion of the addition, the reaction was concentrated and the residue was partitioned between water and dichloromethane. The layers separated and the aqueous was back extracted with dichloromethane. The combined organic layers were washed with water, dried over magnesium sulfate and concentrated. The crude residue was purified by normal phase chromatography (1% MeOH in dichloromethane to 5% MeOH) to give the desired product (20 mg).
MS (ESP): 520 (M+1) for C22H20F3N7OS
1H-NMR (DMSO-d6) δ: 1.10 (t, 3H); 1.40 (d, 6H); 3.10-3.26 (m, 2H); 3.43-3.63 (m, 1H); 7.55 (brs, 1H); 8.23 (s, 1H); 8.28 (s, 1H); 8.41 (s, 1H); 8.56 (s, 1H); 8.64 (d, 1H); 9.16 (d, 1H); 9.50 (s, 1H).
Diisopropylethylamine (0.061 mL, 0.35 mmol) and carbonyldiimidazole (56.6 mg, 0.35 mmol) were added to a solution of 1-ethyl-3-(5′-(hydrazinecarbonyl)-4-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridin-6-yl)urea (Intermediate 9, 105 mg, 0.23 mmol) in DMF (1.5 mL), and the mixture was stirred at room temperature for 1.5 hours. The reaction was diluted with water and extracted with 5% methanol in dichloromethane. The combined extract was washed with water, brine, dried over magnesium sulfate and concentrated under reduced pressure. The crude residue obtained was purified by normal phase chromatography (2% MeOH in dichloromethane to 8% MeOH) to give the desired compound as a white solid (65 mg).
MS (ESP): 478 (M+1) for C19H14F3N7O3S
1H-NMR (DMSO-d6) δ: 1.10 (t, 3H); 3.16-3.28 (m, 2H); 7.55 (brs, 1H); 8.09 (s, 1H); 8.22 (s, 1H); 8.37 (s, 1H); 8.57 (s, 1H); 8.62 (s, 1H); 8.97 (s, 1H); 9.50 (s, 1H); 12.80 (s, 1H).
N-(1-(dimethylamino)ethylidene)-6′-(3-ethylureido)-4′-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridine-5-carboxamide (Intermediate 10, 80 mg, 0.16 mmol) was added to a solution of acetohydrazide (12.90 mg, 0.17 mmol) in acetic acid (2 mL), and the resulting solution was heated at 90° C. for one hour. Then the reaction was concentrated, diluted with water and extracted with dichloromethane. During the work up process, the product started to precipitate. The mixture was washed with a 1M potassium carbonate solution twice and the precipitate was collected by filtration and dried to give the product as a white solid (35 mg).
MS (ESP): 475 (M+1) for C20H17F3N8OS
1H-NMR (DMSO-d6) δ: 1.10 (t, 3H); 2.31 (s, 3H); 3.12-3.26 (m, 2H); 7.74 (brs, 1H); 8.18 (s, 1H); 8.27 (s, 1H); 8.34 (s, 1H); 8.38 (s, 1H); 8.51 (s, 1H); 9.14 (d, 1H); 9.61 (s, 1H).
N-(1-(dimethylamino)ethylidene)-6′-(3-ethylureido)-4′-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridine-5-carboxamide (Intermediate 10, 80 mg, 0.16 mmol) was added to a solution of hydroxylamine hydrochloride (13.20 mg, 0.19 mmol) in a mixture of sodium hydroxide (0.038 mL, 0.19 mmol) and 70% aq acetic acid (2 mL), and 3 ml of dioxane. The resulting mixture was slowly warmed to temperature 80° C. Most of the solid went into solution at 35° C. and solid precipitated out of solution at 50° C. The mixture was allowed to stir for 30 minutes then concentrated. The residue was partitioned between with water and dichloromethane, the layers separated and the aqueous layer was back extracted 2-3 times. During the process, the product started to precipitate. The mixture was washed with saturated sodium bicarbonate solution and water. Then the precipitated product was filtered off and dried to give the title compound as a white solid (55 mg).
MS (ESP): 476 (M+1) for C20H16F3N7O2S
1H-NMR (DMSO-d6) δ: 1.10 (t, 3H); 2.31 (s, 3H); 3.05-3.28 (m, 2H); 7.74 (brs, 1H); 8.24 (s, 1H); 8.40 (s, 2H); 8.56 (s, 1H); 8.77 (d, 1H); 9.25 (d, 1H); 9.60 (s, 1H).
Methyl 2-(6-(3-ethylureido)-4-(4-(trifluoromethyl)thiazol-2-yl)pyridin-3-yl)thiazole-5-carboxylate (Intermediate 13; 128 mg, 0.28 mmol) was suspended hydrazine hydrate (0.2 mL, 6.43 mmol) and ethanol (5 mL). The slurry was heated until it became homogeneous. The reaction was monitored by LC/MS, and once it was determined to be complete, the reaction mixture concentrated to dryness. The solids were suspended in THF (5 mL) and diisopropylethylamine (0.073 mL, 0.42 mmol) and di(1H-imidazol-1-yl)methanone (45.4 mg, 0.28 mmol) were added. The mixture was heated to reflux, and the product precipitated out of solution. The solids were filtered and washed with methanol, then dried in vacuo. Isolation gave 24 mg of the title compound.
MS (ESP): 484 (M+1) for C17H12F3N7O3S2.
1H NMR (300 MHz, d6-DMSO): 1.03 (t, 3H), 3.14 (m, 2H), 7.42 (t, 1H), 8.03 (s, 1H), 8.30 (s, 1H), 8.66 (s, 1H), 8.68 (s, 1H), 9.63 (s, 1H), 12.73 (s, 1H).
1,1′-Carbonylbis-1H-imidazole (0.050 g, 0.31 mmol) and DIEA (0.053 mL, 0.31 mmol) were added to a suspension of N-ethyl-N′45′-(hydrazinocarbonyl)-4-(4-pyridin-2-yl-1,3-thiazol-2-yl)-3,3′-bipyridin-6-yl]urea (Intermediate 22, 94 mg, 0.31 mmol) in DMF (2 mL), and the mixture was stirred at room temperature for 4 hours. The reaction mixture was concentrated under reduced pressure, then purified by Gilson HPLC (5-95% ACN/0.1% TFA in 14 min). Isolation gave 19 mg of the title compound.
LC/MS (ES+)[(M+H)+]: 487 for C23H18N8O3S.
1H NMR (300 MHz, d6-DMSO): 1.11 (t, 3H), 3.22 (m, 2H), 7.36 (t, 1H), 7.62 (t, 1H), 7.67 (d, 1H), 7.84 (m, 1H), 8.21 (t, 1H), 8.28 (s, 1H), 8.34 (s, 1H), 8.37 (s, 1H), 8.6 (d, 1H), 8.70 (d, 1H), 8.98 (d, 1H), 9.39 (s, 1H), 12.79 (s, 1H).
The following compounds have been synthesized as described for Example 10 from the starting materials indicated in the table below.
A reaction mixture of 1-ethyl-3-(5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-4-(4-(trifluoromethyl)thiazol-2-yl)pyridin-2-yl)urea (Intermediate 12, 100 mg, 0.23 mmol), 6-bromoquinoxaline (43.0 mg, 0.21 mmol), Tetrakis (23.75 mg, 0.02 mmol), and cesium carbonate (73.7 mg, 0.23 mmol) in dioxane and water was prepared. The reaction mixture was degassed with nitrogen for 15 minutes and then heated to 100° C. for 1 h. The reaction mixture was partitioned between methylene chloride and water. The organic layer was washed with saturated sodium chloride, dried over sodium sulfate, filtered, and concentrated under reduced pressure. Purification by flash column chromatography (silica, 15:1 methylene chloride/methanol) gave 44 mg of desired product.
MS (ESP): 445 (M+1) for C20H15F3N6OS.
1H NMR (300 MHz, DMSO-d6): 1.12 (t, J=7 Hz, 3H), 3.24 (m, 2H), 7.23 (m, 1H), 7.43 (m, 1H), 8.04 (m, 1H), 8.21 (m, 1H), 8.36 (m, 1H), 8.55 (m, 1H), 9.02 (br s, 2H), 9.36 (s, 1H), 9.52 (s, 1H).
1-(5-Bromo-4-(4-(trifluoromethyl)thiazol-2-yl)pyridin-2-yl)-3-ethylurea (Intermediate 3, 70 mg, 0.18 mmol), 3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine, cesium carbonate (115 mg, 0.35 mmol), tetrakis(triphenylphosphine)palladium (0) (20.47 mg, 0.02 mmol) were taken in a microwave vial and degassed with nitrogen. Then dioxane:water (4:1, 5 mL) was added and the resulting mixture was heated in a microwave at 100° C. for 30 minutes. The palladium catalyst was filtered off and the filtrate was partitioned between water and ethyl acetate. The layers were separated and the aqueous layer was back extracted with ethyl acetate three times. The combined organic extract was washed with water and brine, dried over magnesium sulfate and concentrated under reduced pressure. The crude residue was washed with acetonitrile several times to give off-white solid (42 mg).
MS (ESP): 394 (M+1) for C17H14F3N5OS
1H-NMR (DMSO-d6) δ: 1.09 (t, 3H); 3.17-3.22 (m, 2H); 7.44-7.50 (m, 1H); 7.55 (t, 1H); 7.76 (d, 1H); 8.20 (s, 1H); 8.30 (s, 1H); 8.49 (s, 1H); 8.55 (s, 1H); 8.64 (d, 1H); 9.45 (s, 1H).
1-Ethyl-3-(5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-4-(4-(trifluoromethyl)thiazol-2-yl)pyridin-2-yl)urea (Intermediate 12, 150 mg, 0.34 mmol), 3-bromopyridine 1-oxide, tetrakis(triphenylphosphine)palladium (0) (39.2 mg, 0.03 mmol), cesium carbonate (221 mg, 0.68 mmol) were taken in a microwave vial and degassed with nitrogen. Then dioxane:water (4:1, 5 mL) was added and the resulting mixture was heated in a microwave at 100° C. for 30 minutes. The product precipitated from the reaction as a white solid and was collected by filtration and washed with water and 1% methanol in dichloromethane to provide the desired product (27 mg).
MS (ESP): 410 (M+1) for C17H14F3N5O2S
1H-NMR (DMSO-d6) δ: 1.09 (t, 3H); 3.12-3.22 (m, 2H); 7.23 (d, 1H); 7.40-7.45 (m, 1H); 7.45 (brs, 1H); 8.19 (s, 1H); 8.27 (d, 1H); 8.29 (s, 1H); 8.31 (s, 1H); 8.61 (s, 1H); 9.48 (s, 1H).
A solution of diethyl 2-(6-(3-ethylureido)-4-(4-(trifluoromethyl)thiazol-2-yl)pyridin-3-yl)thiazole-4,5-dicarboxylate (Intermediate 25, 150 mg, 0.28 mmol) and hydrazine hydrate (0.4 mL, 1.0N in MeOH) in methanol (10 mL) was refluxed for 5 h. The mixture was cooled and additional 0.4 mL of hydrazine hydrate-MeOH solution was added. The mixture was stirred for additional 5 h. The reaction mixture was cooled and 1.0 N HCl (1 mL) was added. The mixture was stirred at 45° C. for 1 h, cooled to room temperature, neutralized with powdered NaHCO3, then purified via a reverse phase C18 column (10%-75% MeOH-water) to afford 70 mg (53%) of desired product as off-white powder.
MS (ESP): 484.0 (M+H+) for C17H12F3N7O3S2
1H NMR (DMSO-d6): δ ppm 1.11 (t, 3H), 3.21 (m, 2H), 7.46 (t, 1H), 8.16 (s, 1H), 8.72 (d, 1H), 8.78 (s, 1H), 9.78 (s, 1H)
1-Ethyl-3-(5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-4-(4-(trifluoromethyl)thiazol-2-yl)pyridin-2-yl)urea (Intermediate 12, 140 mg, 0.32 mmol), 5-(5-bromopyridin-3-yl)-1H-pyrazol-3(2H)-one (Intermediate 26, 76 mg, 0.32 mmol), cesium carbonate (103 mg, 0.32 mmol), tetrakis(triphenylphosphine)palladium(0) (36.6 mg, 0.03 mmol) and water (1.500 mL) were taken in a microwave vial and degassed with nitrogen. Then dioxane:water (8 mL 4:1) was added and the reaction mixture was heated in a microwave at 100° C. for 2 h. The reaction mixture was diluted with water and extracted with 5% MeOH in dichloromethane. The combined extract was dried over magnesium sulfate and concentrated under reduced pressure. The crude product was purified by reverse phase HPLC (25% to 70% ACN in water, 0.01% TFA). The fractions containing the product were combined, concentrated under reduced pressure and lypholized to give a white solid (42 mg) that was triturated with acetonitrile and dried under high vacuum.
MS (ESP): 476 (M+1) for C20H16F3N7O2S
1H-NMR (DMSO-d6) δ: 1.11 (t, 3H); 3.16-3.24 (m, 2H); 6.05 (s, 1H); 7.58 (brs, 1H); 8.18 (s, 1H); 8.28 (s, 1H); 8.38 (s, 1H); 8.45 (s, 1H); 8.56 (s, 1H); 9.01 (s, 1H); 9.51 (s, 1H).
DBU (0.080 mL, 0.53 mmol) followed by di(1H-imidazol-2-yl)methanethione (35.5 mg, 0.20 mmol) were added to a mixture of 6′-(3-ethylureido)-N-hydroxy-4′-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridine-5-carboximidamide (Intermediate 27, 60 mg, 0.13 mmol) in acetonitrile (3 mL), and the mixture was stirred at room temperature overnight. The reaction was concentrated and the residue was partitioned between water and ethyl acetate. The layers were separated and the organic layer was washed with water and brine, then dried over magnesium sulfate and concentrated under reduced pressure. The residue was purified by reverse phase chromatography and the fractions containing the product were combined and lyophilized to give white solid (22 mg, low yield).
MS (ESP): 494 (M+1) for C19H14F3N7O2S2
1H-NMR (DMSO-d6) δ: 1.10 (t, 3H); 3.16-3.24 (m, 2H); 7.56 (brs, 1H); 8.23 (s, 1H); 8.24 (s, 1H); 8.37 (s, 1H); 8.58 (s, 1H); 8.70 (d, 1H); 9.06 (s, 1H); 9.52 (s, 1H).
DBU (0.023 mL, 0.16 mmol) followed by carbonyl diimidazole (25.1 mg, 0.16 mmol) were added to a suspension of 6′-(3-ethylureido)-N′-hydroxy-4′-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridine-5-carboximidamide (Intermediate 27, 70 mg, 0.16 mmol) in dioxane (3 mL). The resulting solution was stirred overnight at room temperature. The solvent was removed and the crude residue was partitioned between water and ethyl acetate. The layers were separated and the aqueous was back extracted with ethyl acetate three times. The aqueous layer was concentrated under reduced pressure and purified by reverse phase HPLC (5% ACN in water to 70% ACN) to give the title compound as a white solid (33 mg).
MS (ESP): 478 (M+1) for C19H14F3N7O3S
1H-NMR (DMSO-d6) δ: 1.09 (t, 3H); 3.15-3.24 (m, 2H); 7.51 (br s, 1H); 8.15 (s, 1H); 8.24 (s, 1H); 8.37 (s, 1H); 8.59 (s, 1H); 8.70 (s, 1H); 8.99 (d, 1H); 9.52 (s, 1H); 13.14 (br s, 1H).
To a suspension of 6′-(3-ethylureido)-N-hydroxy-4′-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridine-5-carboximidamide (Intermediate 27, 70 mg, 0.16 mmol) in THF (1.5 mL) at 0° C., pyridine (0.025 mL, 0.31 mmol) was added followed by a drop wise addition of a solution of sulfurous dichloride (0.023 mL, 0.31 mmol) in dichloromethane (1.5 mL). The resulting mixture was slowly warmed up to room temperature and allowed to stir for an hour. Then the reaction was quenched by adding water (1 mL). The layers were separated and the aqueous layer was back extracted with 1% MeOH in DCM twice and the combined organic layers were washed with water and brine, then dried over magnesium sulfate, filtered and concentrated under reduced pressure. The resulting residue was purified by normal phase chromatography to give the title compound as a white solid (25 mg).
MS (ESP): 498 (M+1) for C18H14F3N7O3S2
1H-NMR (DMSO-d6) δ: 1.10 (t, 3H); 3.18-3.22 (m, 2H); 7.58 (br s, 1H); 8.17 (t, 1H); 8.25 (s, 1H); 8.36 (s, 1H); 8.54 (d, 1H); 8.57 (d, 1H); 9.04 (d, 1H); 9.50 (br s, 1H).
3-Bromo-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine (596 mg, 2.10 mmol), 1-(5-bromo-4-(4-(trifluoromethyl)thiazol-2-yl)pyridin-2-yl)-3-ethylurea (Intermediate 3, 830 mg, 2.10 mmol), tris(dibenzylideneacetone)dipalladium(0) (192 mg, 0.21 mmol), 2-dicyclohexylphosphino-2′,4′,6′-tri-iso-propyl-1,1′-biphenyl (300 mg, 0.63 mmol) and sodium carbonate (223 mg, 2.10 mmol) were taken in a round bottomed flask, and the flask was flushed with nitrogen. Solvent (5:1; acetonitrile, water, 10 mL) was added and degassed with nitrogen, and the mixture was heated at 100° C. for 3 h. The reaction mixture was filtered and the filtrate was concentrated under reduced pressure. The resulting crude residue was partitioned between water and ethyl acetate. The layers were separated and the aqueous was back extracted with ethyl acetate three times. The combined organic layers were washed with water and brine, dried over magnesium sulfate and concentrated under reduced pressure. The residue obtained was purified by normal phase chromatography (gradient of MeOH in DCM) to give a white solid (483 mg).
MS (ESP): 473 (M+1) for C17H13BrF3N5OS
The following Examples were synthesized according to the procedure described for Intermediate 2 from the starting materials indicated.
Sodium methoxide (10.291 μl, 0.06 mmol) was added to a suspension of 1-(5′-cyano-4-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridin-6-yl)-3-ethylurea (Example 2, 120 mg, 0.29 mmol) in methanol (3 mL), and the resulting mixture was stirred overnight at room temperature. 2,2-Dimethoxyethanamine (30.9 μl, 0.29 mmol) followed by acetic acid (32.8 μl, 0.57 mmol) were added, and the mixture was heated to 50° C. for 1.5 hours. The reaction mixture was cooled to room temperature and isopropanol (3 mL) followed by HCl (500 μl, 6N) were added and the mixture was refluxed overnight. The solvent was removed and the residue was dissolved in water and neutralized by adding 2N NaOH. The aqueous layer was extracted with ethyl acetate, and the ethyl acetate layer was washed with water and brine, dried over magnesium sulfate, and concentrated under reduced pressure. The off-white solid obtained was triturated with acetonitrile and dried to give a white solid (43 mg).
MS (ESP): 460 (M+1) for C20H16F3N7OS
1H-NMR (DMSO-d6) δ: 1.11 (t, 3H); 3.14-3.25 (m, 2H); 7.09 (s, 1H); 7.35 (s, 1H); 7.58 (brs, 1H); 8.24 (s, 1H); 8.28 (s, 1H); 8.37 (s, 1H); 8.43 (s, 1H); 8.53 (s, 1H); 9.19 (s, 1H); 9.49 (s, 1H); 12.73 (s, 1H).
Bismuth(III) trifluoromethanesulfonate (10.98 mg, 0.02 mmol) was added to a suspension of 1-(5′-cyano-4-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridin-6-yl)-3-ethylurea (Example 2, 100 mg, 0.24 mmol) and 2-aminoethanol (115 μl, 1.91 mmol), and the resulting reaction mixture was stirred at 70° C. for overnight. The reaction mixture was partitioned between water and 3% MeOH in ethyl acetate. The layers were separated and the aqueous layer was back extracted twice with 3% methanol in ethyl acetate. The combined organic layers were dried over magnesium sulfate and concentrated under reduced pressure to give a white solid. The solid was triturated with acetonitrile and dried under high vacuum to give the product as a white solid (26 mg).
MS (ESP): 463 (M+1) for C20H17F3N6O2S
1H-NMR (DMSO-d6) δ: 1.11 (t, 3H); 3.14-3.28 (m, 2H); 3.99 (t, 2H); 4.43 (t, 2H); 7.57 (t, 1H); 8.12 (t, 1H); 8.23 (s, 1H); 8.36 (s, 1H); 8.56 (s, 1H); 8.65 (d, 1H); 9.04 (s, 1H); 9.50 (s, 1H).
The following Examples were synthesized according to the procedure described for Example 10 from the starting materials indicated.
In a microwave reaction vessel, 1-(5-bromo-4-(4-(trifluoromethyl)thiazol-2-yl)pyridin-2-yl)-3-ethylurea (Intermediate 3, 200 mg, 0.51 mmol), 2-(1H-pyrazol-1-yl)-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine (137 mg, 0.51 mmol) and cesium carbonate (64.4 mg, 0.61 mmol) were combined and suspended in a 4:1 mixture of dioxane and water. Pd(PPh3)4 (29.2 mg, 0.03 mmol) was added in a single portion. The vessel was sealed, degassed, purged with nitrogen and heated to 100° C. in the microwave for 120 min. The crude reaction mixture was concentrated to dryness. The resulting residue was dissolved in DMSO, filtered and then purified by Gilson HPLC (5-95% ACN/0.1% TFA water in 14 minutes). Isolation gave 56 mg of the title compound.
LC/MS (ES+)[(M+H)+]: 460 for C20H16F3N7OS.
1H NMR (300 MHz, d6-DMSO): 1.11 (t, 3H), 3.20 (m, 2H), 6.47 (m, 1H), 7.59 (d, 1H), 7.61 (m, 1H), 7.79 (m, 1H), 7.85 (d, 1H), 7.95 (d, 1H), 8.06 (m, 2H), 8.55 (m, 1H), 8.62 (s, 1H), 9.56 (s, 1H).
In a microwave reaction vessel, 1-(5-bromo-4-(4-(trifluoromethyl)thiazol-2-yl)pyridin-2-yl)-3-ethylurea (Intermediate 3, 100 mg, 0.25 mmol), 4-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiazol-2-yl)morpholine (82 mg's, 0.28 mmol), sodium carbonate (40 mg, 0.38 mmol), Pd2(dba)3 (23.17 mg, 0.03 mmol) and X-Phos (2-(Dicyclohexylphosphino)-2′,4′,6′-tri-1-propyl-1,1′-biphenyl) (38.1 mg, 0.08 mmol) were combined and suspended in 4:1 mixture of acetonitrile (3 mL) and water (0.75 mL). The vessel was sealed and heated to 90° C. in an oil bath for 30 min. The reaction mixture was cooled to room temperature and concentrated to dryness. The crude residue was dissolved in minimal DMSO, filtered and then purified by Gilson HPLC (5-95% ACN/0.1% TFA water in 14 min.). Isolation gave 58 mg of the compound.
LC/MS (ES+)[(M+H)+]: 485 for C19H19F3N6O2S2.
1H NMR (300 MHz, d6-DMSO): 1.03 (t, 3H), 3.11 (m, 2H), 3.18 (m, 4H), 3.58 (m, 4H), 7.01 (s, 1H), 7.54 (t, 1H), 8.00 (s, 1H), 8.35 (s, 1H), 8.56 (s, 1H), 9.31 (s, 1H).
The following Examples were synthesized according to the procedure for Example 30 from the starting materials indicated below.
6-(3-Ethylureido)-4-(4-(trifluoromethyl)thiazol-2-yl)-3,4′-bipyridine-2′-carboxylic acid (Intermediate 50, 72.1 mg, 0.16 mmol) was dissolved in a DMF solution containing diisopropylethyl amine (0.057 mL, 0.33 mmol) and HATU (75 mg, 0.20 mmol). The solution was allowed to stir for 30 min., then hydrazine monohydrate (0.052 mL, 1.65 mmol) was added in a single in portion. The reaction mixture was diluted with EtOAc then washed with water. The organic layer was dried over Na2SO4, filtered and concentrated under reduced pressure.
The crude reaction mixture was dissolved in THF (2 mL) and carbonyl diimidazole (66 mg, 0.41 mmol) was added in a single portion. The reaction mixture was heated to reflux in a sealed microwave vial. The crude reaction mixture was concentrated under reduced pressure. The resulting residue was treated with water and the solid that formed was collected by filtration, washed with water and dried in vacuo. Isolation gave 61 mg of the crude product. The crude product was dissolved in minimal DMSO and purified by Gilson HPLC (5-95% ACN/0.1% TFA water in 14 min). Isolation gave 21 mg of the title compound.
LC/MS (ES+)[(M+H)+]: 478 for C19H14F3N7O3S.
1H NMR (300 MHz, d6-DMSO): 1.04 (t, 3H), 3.12 (m, 2H), 7.43 (d, 1H), 7.46 (t, 1H), 7.73 (s, 1H), 8.10 (s, 1H), 8.32 (s, 1H), 8.55 (s, 1H), 8.62 (d, 1H), 9.49 (s, 1H), 12.74 (s, 1H).
The following Examples were prepared according to the procedure described for Example 9 from the indicated starting materials.
6-Butoxy-6′-(3-ethylureido)-4′-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridine-5-carboxylic acid (Intermediate 57, <100 mg) was stirred in anhydrous MeOH in the presence of catalytic amount of SOCl2 overnight at rt. The mixture was concentrated and the residue was dissolved in EtOH, and treated with >10 eq. of hydrazine hydrate at 70-80° C. for 48 h. The mixture was concentrated and residue was purified via a reverse phase column (10-60% EtOH-water). The hydrazide product was dissolved in THF, treated with 1.5 eq. of carbonyl diimidazole and Et3N at room temperature for 1 h. The reaction mixture was concentrated and purified via a silica gel column chromatograph with heptane-EtOAc (1:1)+2% EtOH to give a 15% yield of 1-(6′-butoxy-5′-(5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)-4-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridin-6-yl)-3-ethylurea.
MS (ESP): 550.2 (M+H+) for C23H22F3N7O4S.
1H NMR (CD3OD): δ ppm 0.99 (t, 3H), 1.22 (t, 3H), 1.43-1.59 (m, 2H), 1.75-1.83 (m, 2H), 3.31 (q, 2H), 4.49 (t, 2H), 7.87 (s, 1H), 7.99 (d, 1H), 8.16 (d, 1H), 8.21 (d, 1H), 8.32 (d, 1H)
The following Example was prepared according to the procedure for Example 1 from the starting materials indicated.
To a 100 mL of round bottom flask was charged methyl 6′-(3-isopropylureido)-4′-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridine-5-carboxylate (Intermediate 79, 80 mg, 0.172 mmol) with ethanol (20 mL), then hydrazine monohydrate (3 mL) was added. The mixture was heated at reflux for 1.5 h. The mixture was concentrated under reduced pressure to give a white solid. To the crude material was charged anhydrous tetrahydrofuran (20 mL) with 1,1′-carbonyl diimidazole (1.43 g). The mixture was allowed to stir at room temperature overnight. The mixture was concentrated to dryness, water was added and the mixture was allowed to stand for 1-2 hours. A white solid precipitated from the water and was collected then dried in vacuo overnight at 50° C. to give a white solid (56 mg, 66.4%).
MS (ESP): 492.0 (MH+) for C20H16F3N7O3S
1H NMR (300 MHz, CD3OD): δ 1.25 (d, 6H), 3.99 (m, 1H), 7.90 (s, 1H), 8.17 (t, 1H), 8.25 (d, 1H), 8.37 (d, 1H), 8.57 (d, 1H), 9.00 (d, 1H)
19F NMR (CD3OD) −66.00
The following Examples were prepared as described for Example 42 from the starting materials indicated in the Table.
Methyl 6′-(3-ethylureido)-4′-(5-((2-morpholinoethylamino)methyl)-4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridine-5-carboxylate (Intermediate 98, 0.35 mmol) was dissolved in tetrahydrofuran (5 mL) and saturated sodium bicarbonate solution (3 mL) was added followed by di-tert-butyl dicarbonate (0.7 mmol) and the reaction was stirred at room temperature for 96 hours at 35° C. Ethyl acetate (10 mL) was added, the layers separated and the solvent was removed in vacuo. The residue was dissolved in ethanol (20 mL), hydrazine monohydrate (1 mL) was added and the solution stirred at room temperature for 3 hours. The solvent was removed in vacuo, and the residue was twice suspended in 2:1 toluene:tetrahydrofuran (10 mL) and the solvent was removed in vacuo. This residue was then dissolved in anhydrous tetrahydrofuran (10 mL) and 1,1′-carbonyl diimidazole (500 mg) was added. The reaction was stirred at room temperature for 5 hours and the solvent was removed. The residue was chromatographed on an 8 g Analogix silica gel column eluting with 0-10% methanol in dichloromethane. The product containing fractions were combined and subjected to further HPLC purification using water and acetonitrile. The product fractions were combined, and hydrochloric acid (1 mL) was added. As the solvent was removed from the product on a rotovap at 45° C., the Boc group was cleaved to give final product (18% yield)
MS (ESP): 620.1 (M+H+) for C26H31Cl3F3N9O4S
1H NMR (300 MHz, DMSO-d6): δ 1.11 (t, 3H), 3.19-3.22 (m, 2H), 3.42-3.52 (m, 4H), 3.80-3.99 (m, 4H), 4.58 (s, 2H), 7.52 (bt, 1H), 8.18 (t, 1H), 8.29 (s, 1H), 8.38 (s, 1H), 8.64 (d, 1H), 8.99 (d, 1H), 9.63 (s, 1H), 12.88 (s, 1H).
The following compounds were prepared according to the procedure described for Example 51 from the starting material as indicated in the Table.
Methyl 6′-(3-ethylureido)-4′-(5-((2-methoxyethylamino)methyl)-4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridine-5-carboxylate (Intermediate 97, 200 mg) was dissolved in tetrahydrofuran (3 mL) and methanol (3 mL). 1N Sodium hydroxide (3 mL) was added, and the reaction mixture was stirred at room temperature for 3 h. The organics were removed and the residual aqueous phase was acidified to pH ˜2 with 1N hydrochloric acid. The water was then removed in vacuo. The residue was dissolved in phosphorous oxychloride (3 mL), acetic hydrazide (200 mg) was added and the solution heated at 60° C. for 3 hours. Most of the phosphorous oxychloride was removed in vacuo and then saturated sodium bicarbonate was added to pH ˜7. The solution was extracted with 2:1 ethyl acetate: tetrahydrofuran (3×, 3 mL each). The organic phases were combined, dried over sodium sulfate, and the solvent was removed in vacuo. The crude product was chromatographed on a 4 g Analogix silica gel column using 0-10% methanol in dichloromethane.
MS (ESP): 563.1 (M+H+) for C24H25F3N8O3S
1H NMR (300 MHz, DMSO-d6): δ 1.22 (t, 3H), 2.63 (s, 3H), 2.71 (t, 2H), 3.31 (s, 3H), 3.31-3.41 (m, 4H), 4.07 (d, 2H), 7.79 (s, 1H), 8.34-8.36 (m, 2H), 8.63 (d, 1H), 9.17 (d, 1H).
The following Examples were prepared according to the procedure described for Example 54 from the starting materials indicated in the Table.
To a 50 mL round bottom flask was added methyl 6′-(3-ethylureido)-4′-(5-(2-methoxyethylcarbamoyl)-4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridine-5-carboxylate (Intermediate 104, 80 mg), ethanol (10 mL) and hydrazine (0.3 mL) and the solution heated to reflux for 3 h. The solvent was removed in vacuo and the residue evaporated from toluene (3×, 60 mL) to remove excess hydrazine. The yellowish gum was then dried at 50° C. in a vacuum oven overnight. The crude solid was re-dissolved in tetrahydrofuran (10 mL), then triethylamine (1 mL) and 1,1′-carbonyl diimidazole (0.5 g) were added. The solution was then stirred at room temperature for 2 hrs. The solvent was removed under reduced pressure, DIUF water (10 mL) was added, and the mixture was stirred for 30 min. A white solid precipitated out which was filtered and dried to give 40 mg product as off-white solid.
MS (ESP): 579.0 (M+H+) for C23H21F3N8O5S
1H NMR (300 MHz, DMSO-d6): δ 1.11 (t, 3H), 3.21 (m, 2H), 3.24 (s, 3H), 3.36 (m, 4H), 7.01 and 7.64 (bs, tautomers, 1H), 7.49 (t, 1H), 8.20 (m, 1H), 8.26 (s, 1H), 8.37 (s, 1H), 8.64 (d, 1H), 9.01 (m, 2H), 9.52 (bs, 1H).
To a 50 mL round bottom flask was added crude 6′-(3-ethylureido)-4′-(5-(2-methoxyethylcarbamoyl)-4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridine-5-carboxylic acid (Intermediate 105, 90 mg), phosphorus oxychloride (3 mL) and acetyl hydrazine (0.2 g). The solution was then heated to 65° C. for 3 h after which time no starting material remained by LC/MS (LC purity was ˜40%). The solvent was removed under reduced pressure and toluene (3×, 60 mL) was added to remove excess phosphorus oxychloride. Saturated sodium bicarbonate was then added until pH ˜7. The solution was extracted with ethyl acetate (3×, 100 mL). The combined organics were dried over sodium sulfate, filtered, and concentrated. The residue was dissolved in methanol and purified by prep HPLC to give 20 mg light yellow solid.
MS (ESP): 577.2 (M+H+) for C24H23F3N8O4S
1H NMR (300 MHz, CD3OD): δ 1.22 (t, 3H), 2.35 and 2.64 (s, 3H), 3.30 (m, 6H), 3.47 (s, 3H), 7.91 (s, 1H), 8.39 (m, 2H), 8.67 (d, 1H), 9.21 (s, 1H).
To a 50 mL round bottom flask was added methyl 6′-(3-ethylureido)-4′-(5-(2-morpholinoethylcarbamoyl)-4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridine-5-carboxylate (Intermediate 106, 200 mg), ethanol (10 mL) and hydrazine (0.5 mL) and the solution heated to reflux for 3 h. The solvent was removed in vacuo and the residue evaporated from toluene (3×, 60 mL) to remove excess hydrazine. The crude intermediate was then dried at 50° C. in a vacuum oven overnight. The solid was re-dissolved in tetrahydrofuran (10 mL), then triethylamine (1 mL) and 1,1′-carbonyl diimidazole (0.5 g) were added. The solution was then allowed to stir at room temperature for 2 hrs. The solvent was removed under reduced pressure and water (10 mL) was added. The mixture was stirred at room temperature overnight however no product precipitated. The crude solution was then purified on a 30 g Analogix C18 column (water/methanol: 40% MeOH/H2O) to give 60 mg light yellow solid.
MS (ESP): 634.2 (M+H+) for C26H26F3N9O5S
1H NMR (300 MHz, DMSO-d6): δ 1.11 (t, 3H), 2.36 (m, 8H), 3.21 (m, 2H), 3.52 (m, 4H), 7.02 and 7.63 (bs, tautomers, 1H), 7.51 (t, 1H), 8.17 (t, 1H), 8.27 (s, 1H), 8.36 (s, 1H), 8.62 (d, 1H), 8.85 (t, 1H), 8.99 (d, 1H), 9.53 (s, 1H).
To a 50 mL round bottom flask was added crude 6′-(3-ethylureido)-4′-(5-(2-morpholinoethylcarbamoyl)-4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridine-5-carboxylic acid (Intermediate 107, 200 mg), phosphorus oxychloride (3 mL) and acetyl hydrazine (0.2 g) and the solution heated to 65° C. for 3 h. The solvent was removed under reduced pressure and toluene (3×, 60 mL) was added to remove excess phosphorus oxychloride. Saturated sodium bicarbonate was added until pH ˜7 and the solution was extracted with ethyl acetate (3×, 100 mL). The combined organics were dried over sodium sulfate, filtered, and concentrated. The residue was then dissolved in methanol and purified by prep HPLC to give 60 mg light yellow solid.
MS (ESP): 632.1 (M+H+) for C27H28F3N9O4S
1H NMR (300 MHz, CD3OD): δ 1.22 (t, 3H), 2.50 (m, 6H), 2.62 and 2.64 (s, 3H), 3.34 (m, 2H), 3.44 (t, 2H), 3.64 (t, 4H), 7.92 (s, 1H), 8.41 (m, 2H), 8.68 (d, 1H), 9.21 (s, 1H).
To a 50 mL round bottom flask was added methyl 6′-(3-ethylureido)-4′-(5-(2-(4-methylpiperazin-1-yl)ethylcarbamoyl)-4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridine-5-carboxylate (Intermediate 108, 300 mg), ethanol (10 mL) and hydrazine (0.5 mL) and the solution heated to reflux for 3 hrs. The solvent was removed in vacuo and the residue evaporated from toluene (3×, 60 mL) to remove excess hydrazine. The crude yellowish gum was then dried at 50° C. in a vacuum oven overnight. The crude solid was re-dissolved in tetrahydrofuran (10 mL), 1,1′-carbonyl diimidazole (0.5 g) was added and the solution stirred at room temperature for 2 hrs. The solvent was then removed in vacuo. Water (10 mL) was added and the mixture was then left to stir overnight however no product precipitated. The product was purified by prep HPLC (water/acetonitrile) to give 150 mg off-white solid.
MS (ESP): 647.1 (M+H+) for C27H29F3N10O4S
1H NMR (300 MHz, DMSO-d6): δ 1.11 (t, 3H), 2.15 (s, 3H), 2.38 (m, 10H), 3.21 (m, 4H), 7.50 (t, 1H), 8.20 (t, 1H), 8.27 (s, 1H), 8.36 (s, 1H), 8.64 (d, 1H), 8.81 (t, 1H), 9.00 (d, 1H), 9.52 (bs, 1H).
To a 50 mL round bottom flask was added crude 6′-(3-ethylureido)-4′-(5-(2-(4-methylpiperazin-1-yl)ethylcarbamoyl)-4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridine-5-carboxylic acid (Intermediate 109, 200 mg), phosphorus oxychloride (3 mL) and acetyl hydrazine (0.2 g). The solution was then heated at 65° C. for 3 h. The solvent was removed in vacuo and the residue evaporated from toluene (3×, 60 mL) to remove excess phosphorus oxychloride. Saturated sodium bicarbonate was added to pH ˜7 and the solution was extracted with ethyl acetate/tetrahydrofuran (1/1) (5×, 100 mL). The combined organics were dried over sodium sulfate, filtered, and concentrated. The residue was then dissolved in methanol and purified by prep HPLC to give 30 mg pale yellow solid.
MS (ESP): 645.3 (M+H+) for C28H31F3N10O3S
1H NMR (300 MHz, DMSO-d6): δ 1.11 (t, 3H), 2.44 (s, 3H), 2.58 (m, 10H), 2.60 (s, 3H), 3.21 (m, 4H), 7.47 (t, 1H), 8.28 (s, 1H), 8.36 (s, 1H), 8.41 (s, 1H), 8.71 (s, 1H), 8.87 (t, 1H), 9.18 (s, 1H), 9.54 (bs, 1H).
To a 50 mL round bottom flask was added methyl 4′-(5-(cyclopropylcarbamoyl)-4-(trifluoromethyl)thiazol-2-yl)-6′-(3-ethylureido)-3,3′-bipyridine-5-carboxylate (Intermediate 110, 300 mg), ethanol (10 mL) and hydrazine (0.5 mL) and the solution was heated to reflux for 3 hrs. The solvent was removed in vacuo and the residue evaporated from toluene (3×, 60 mL) to remove excess hydrazine. The crude dark yellowish gum was then dried at 50° C. in a vacuum oven overnight. The crude solid was re-dissolved in tetrahydrofuran (10 mL), 1,1′-carbonyl diimidazole (0.5 g) was added and the solution was stirred at room temperature for 2 hrs. The solvent was removed under reduced pressure, water (10 mL) was added and the mixture left to stir at room temperature overnight. The yellow solids were filtered and washed with water to give 80 mg product at ˜80% purity. The material was further purified by prep HPLC (water/acetonitrile) to give 30 mg white solid.
MS (ESP): 561.3 (M+H+) for C23H19F3N8O4S
1H NMR (300 MHz, DMSO-d6): δ 0.48 (m, 2H), 0.69 (m, 2H), 1.11 (t, 3H), 2.76 (m, 1H), 3.22 (m, 2H), 7.78 (t, 1H), 8.19 (s, 1H), 8.24 (s, 1H), 8.37 (s, 1H), 8.63 (s, 1H), 9.00 (s, 2H), 9.52 (bs, 1H).
To a 50 mL round bottom flask was added crude 4′-(5-(cyclopropylcarbamoyl)-4-(trifluoromethyl)thiazol-2-yl)-6′-(3-ethylureido)-3,3′-bipyridine-5-carboxylic acid (Intermediate 111, 200 mg), phosphorus oxychloride (3 mL) and acetyl hydrazine (0.2 g). The solution was then heated at 65° C. for 3 h. The solvent was removed in vacuo and the residue evaporated from toluene (3×, 60 mL) to remove excess phosphorus oxychloride. Saturated sodium bicarbonate was added to pH ˜7 and the solution was extracted with ethyl acetate (3×, 100 mL). The combined organics were dried over sodium sulfate, filtered, and concentrated. The residue was then dissolved in methanol and purified by prep HPLC to give 40 mg pale yellow solid.
MS (ESP): 559.2 (M+H+) for C24H21F3N8O3S
1H NMR (300 MHz, DMSO-d6): δ 0.47 (m, 2H), 0.69 (m, 2H), 1.11 (t, 3H), 2.60 (s, 3H), 2.74 (m, 1H), 3.22 (m, 2H), 7.47 (t, 1H), 8.24 (s, 1H), 8.34 (t, 1H), 8.41 (s, 1H), 8.69 (d, 1H), 8.99 (d, 1H), 9.17 (d, 1H), 9.53 (bs, 1H).
To a 50 mL round bottom flask was added methyl 4′-(5-(cyclopentylcarbamoyl)-4-(trifluoromethyl)thiazol-2-yl)-6′-(3-ethylureido)-3,3′-bipyridine-5-carboxylate (Intermediate 112, 200 mg), ethanol (10 mL) and hydrazine (1.0 mL). The solution was heated to reflux for 3 hrs. The solvent was removed in vacuo and the residue evaporated from toluene (3×, 60 mL) to remove excess hydrazine. The crude dark yellowish gum was then dried at 50° C. in a vacuum oven overnight. The crude solid was re-dissolved in tetrahydrofuran (10 mL), and 1,1′-carbonyl diimidazole (0.5 g) was added. The solution was then allowed to stir at room temperature for 18 hrs. The solvent was removed under reduced pressure, water (10 mL) was added and the mixture was then stirred at room temperature for 3 hours. A yellow solid precipitated out and was filtered and triturated with acetonitrile to give 84 mg of pale yellow solid.
MS (ESP): 589.2 (M+H+) for C25H23F3N8O4S
1H NMR (300 MHz, DMSO-d6): δ 1.11 (t, 3H), 1.35-1.64 (m, 6H), 1.80-1.99 (m, 2H), 3.16-3.23 (m, 2H), 4.06-4.12 (m, 1H), 7.48 (bt, 1H), 8.20 (t, 1H), 8.24 (s, 1H), 8.38 (s, 1H), 8.63 (d, 1H), 8.91 (d, 1H), 9.00 (d, 1H), 9.53 (bs, 1H)
To a 20 mL vial was added crude 4′-(5-(cyclopentylcarbamoyl)-4-(trifluoromethyl)thiazol-2-yl)-6′-(3-ethylureido)-3,3′-bipyridine-5-carboxylic acid (Intermediate 113, 150 mg), phosphorus oxychloride (3 mL) and acetyl hydrazine (0.2 g). The solution was then heated at 60° C. for 3 h. The solvent was removed in vacuo and the residue evaporated from toluene (3×, 60 mL) to remove excess phosphorus oxychloride. Saturated sodium bicarbonate was added to pH ˜7 and the solution extracted with ethyl acetate (3×, 10 mL). The combined organics were dried over sodium sulfate, filtered, and concentrated. The residue was then chromatographed on a 4 g Analogix silica gel column using 0-10% methanol in dichloromethane to give 42 mg of pale yellow solid.
MS (ESP): 587.1 (M+H+) for C26H25F3N8O3S
1H NMR (300 MHz, DMSO-d6): δ 1.11 (t, 3H), 1.39-1.61 (m, 6H), 1.79-1.83 (m, 2H), 2.61 (s, 3H), 3.18-3.25 (m, 2H), 4.02-4.16 (m, 1H), 7.48 (bt, 1H), 8.24 (s, 1H), 8.35 (t, 1H), 8.41 (d, 1H), 8.69 (d, 1H), 8.90 (d, 1H), 9.17 (d, 1H), 9.55 (bs, 1H).
To a 50 mL round bottom flask was added methyl 4′-(5-(cyclohexylcarbamoyl)-4-(trifluoromethyl)thiazol-2-yl)-6′-(3-ethylureido)-3,3′-bipyridine-5-carboxylate (Intermediate 114, 200 mg), ethanol (10 mL) and hydrazine (0.5 mL). The solution was then heated to reflux for 3 hrs. The solvent was removed in vacuo and the residue evaporated from toluene (3×, 60 mL) to remove excess hydrazine. The crude yellowish gum was then dried at 50° C. in a vacuum oven overnight. The crude solid was re-dissolved in tetrahydrofuran (10 mL), 1,1′-carbonyl diimidazole (0.5 g) was added and the solution allowed to stir at room temperature for 2 hrs. The solvent was removed under reduced pressure, water (10 mL) was added and the mixture stirred at room temperature for 2 h. The solids were removed by filtration, triturated with acetonitrile and dried in a vacuum oven at 50° C. for 18 hours to give 73 mg pale yellow solid.
MS (ESP): 603.3 (M+H+) for C26H25F3N8O4S
1H NMR (300 MHz, DMSO-d6): δ 1.11 (t, 3H), 1.12-1.36 (m, 4H), 1.53-1.60 (m, 1H), 1.60-1.78 (m, 5H), 3.16-3.25 (m, 2H), 3.60-3.65 (m, 1H), 7.48 (bt, 1H), 8.21 (t, 1H), 8.24 (s, 1H), 8.37 (s, 1H), 8.63 (d, 1H), 8.84 (d, 1H), 9.00 (d, 1H), 9.53 (s, 1H).
To a 50 mL round bottom flask was added crude 4′-(5-(cyclohexylcarbamoyl)-4-(trifluoromethyl)thiazol-2-yl)-6′-(3-ethylureido)-3,3′-bipyridine-5-carboxylic acid (Intermediate 115, 200 mg), phosphorus oxychloride (3 mL) and acetyl hydrazine (0.2 g). The solution was then heated at 60° C. for 3 h. The solvent was removed in vacuo and the residue evaporated from toluene (3×, 60 mL) to remove excess phosphorus oxychloride. Saturated sodium bicarbonate was added to pH ˜7 and the solution extracted with ethyl acetate (3×, 20 mL). The combined organics were dried over sodium sulfate, filtered, and concentrated. The residue was then chromatographed on a 4 g Analogix silica gel column using 0-10% methanol in dichloromethane to give 53 mg pale yellow solid.
MS (ESP): 601.2 (M+H+) for C27H27F3N8O3S
1H NMR (300 MHz, DMSO-d6): δ 1.11 (t, 3H), 1.12-1.29 (m, 6H), 1.50-1.60 (m, 1H), 1.60-1.78 (m, 3H), 2.60 (s, 3H), 3.16-3.26 (m, 2H), 3.60-3.65 (m, 1H), 7.49 (bt, 1H), 8.25 (s, 1H), 8.35 (t, 1H), 8.41 (s, 1H), 8.69 (d, 1H), 8.83 (d, 1H), 9.17 (d, 1H), 9.55 (bs, 1H).
The following Examples were prepared according to the general procedures described below from the starting materials indicated in the Table.
A methyl ester (0.2 mmol) was suspended in ethanol (10 mL) and anhydrous hydrazine (0.1 mL) was added. The resulting suspension was heated at reflux for 3 h. The solvent was removed in vacuo. Toluene (5 mL) was added to the residue and removed in vacuo twice to remove traces of hydrazine. Anhydrous tetrahydrofuran (10 mL) and 1,1′-carbonyl diimidazole (100 mg) were added, and the reaction was stirred at room temperature for 16 h. The solvent was removed in vacuo and the residue subjected to reverse phase chromatography using 10-99% acetonitrile in water to isolate the product.
The following Examples were prepared according to the general procedures described below from the starting materials indicated in the Table.
The appropriate carboxylic acid (0.1 mmol) and acetic hydrazide (0.15 mmol) were suspended in phosphorous oxychloride (3 mL). The reaction was heated at 65° C. for 3 h. The phosphorous oxychloride was removed in vacuo and toluene (5 mL) was added and also removed in vacuo. Saturated sodium bicarbonate solution (10 mL) was added and the suspension was extracted with 2:1 ethyl acetate:tetrahydrofuran (3×, 5 mL). The organic phases were combined and the solvent was removed in vacuo. The residue was dissolved twice in methyl tert-butyl ether (5 mL each) and the solvent removed in vacuo to remove trace solvents. The residue was given a final trituration with methyl tert-butyl ether (5 mL) and filtered to give the appropriate methyl oxadiazole.
To a 100 mL round bottom flask was charged methyl 6′-ethoxy-6-(3-ethylureido)-4-(4-(trifluoromethyl)thiazol-2-yl)-3,4′-bipyridine-2′-carboxylate (Intermediate 145, 160 mg, 0.323 mmol) with ethanol (20 mL). Hydrazine monohydrate (4 mL) was added and the mixture was heated to reflux for 1 h. After concentrating under reduced pressure, the crude product was further dried in vacuum oven at 50° C. for overnight.
To the crude product was charged tetrahydrofuran (30 mL) with 1,1′-carbonyl diimidazole (160 mg, 0.97 mmol) and the mixture was stirred at room temperature for 0.5 h. Starting material remained so another portion of 1,1′-carbonyl diimidazole (110 mg) was added and the mixture stirred for another 1 h. After concentration under reduced pressure, the crude product was triturated with water. The precipitate was collected by filtration and dried in oven at 60° C. to give a beige solid (140 mg, 83.3% over two steps).
MS (ESP): 522.0 (MH+) for C21H18F3N7O4S
1H NMR (300 MHz, CD3OD): δ 1.22 (t, 3H), 1.39 (t, 3H), 3.31 (q, 2H), 4.45 (q, 2H), 6.86 (d, 1H), 7.32 (d, 1H), 7.79 (s, 1H), 8.26 (s, 1H), 8.35 (s, 1H)
19F NMR (300 MHz, CD3OD): −66.04
To a vial was charged methyl 6′-ethoxy-6-(3-ethylureido)-4-(4-(trifluoromethyl)thiazol-2-yl)-3,4′-bipyridine-2′-carboxylate (Intermediate 145, 200 mg, 0.404 mmol) with tetrahydrofuran (2 mL) and water (2 mL). Lithium hydroxide (100 mg) was added and the resulting mixture was stirred at room temperature overnight. The reaction mixture was diluted with water and methyl tert-butyl ether was added. Solid was observed between the layers and was collected and dried in a vacuum oven at 50° C. overnight.
The carboxylic salt (140 mg) was treated with acetic hydrazide (28 mg, 0.342 mmol) and phosphorus oxychloride (3 mL) then heated at 65° C. for 2 h. The excess phosphorus oxychloride was removed in vacuo and the residue was quenched by saturated sodium bicarbonate (30 mL). The product was extracted with ethyl acetate and tetrahydrofuran (3× each). The organic layers was combined and dried over sodium sulfate. After concentration, the crude mixture was triturated with ethanol (5 mL), and washed with methyl tert-butyl ether (3 mL) to give a white solid (45 mg, 30.4%).
MS (ESP): 520.2 (MH+) for C22H20F3N7O3S
1H NMR (300 MHz, CD3OD): δ 1.22 (t, 3H), 1.39 (t, 3H), 3.31 (q, 2H), 4.45 (q, 2H), 6.86 (d, 1H), 7.32 (d, 1H), 7.79 (s, 1H), 8.26 (s, 1H), 8.35 (s, 1H)
19F NMR (300 MHz, CD3OD): −66.04
To a 100 mL round bottom flask was charged impure methyl 6′-ethoxy-6-(3-ethylureido)-4-(4-phenylthiazol-2-yl)-3,4′-bipyridine-2′-carboxylate (Intermediate 146, 400 mg) with ethanol (40 mL). Hydrazine monohydrate (6 mL) was added and the reaction mixture was heated to reflux for 2 h. After concentrating to dryness, the crude product was triturated with ethanol to remove Pd residue from previous step. The filtrate was concentrated under reduced pressure and dissolved in tetrahydrofuran (30 mL) with 1,1′-carbonyl diimidazole (230 mg, 1.42 mmol), and the mixture was stirred at room temperature overnight. After concentration under reduced pressure, the crude product was purified by Analogix (dichloromethane/methanol) to give an off-white solid (60 mg).
MS (ESP): 530.1 (MH+) for C26H23N7O4S
1H NMR (300 MHz, CD3OD): δ 1.23 (t, 3H), 1.38 (t, 3H), 3.35 (q, 2H), 4.46 (q, 2H), 6.90 (d, 1H), 7.32 (m, 3H), 7.42 (d, 1H), 7.70 (d, 1H), 7.73 (d, 1H), 7.81 (s, 1H), 7.91 (s, 1H), 8.31 (d, 1H)
To a vial was charged methyl 6′-ethoxy-6-(3-ethylureido)-4-(4-phenylthiazol-2-yl)-3,4′-bipyridine-2′-carboxylate (Intermediate 146, 250 mg), tetrahydrofuran (30 mL) and water (30 mL). Lithium hydroxide (500 mg) was added and the resulting mixture was stirred at room temperature overnight. The reaction mixture was diluted with water and a cloudy mixture resulted. Filtration was applied to remove the solid. Methyl tert-butyl ether was added to the filtrate and a white solid precipitated which was collected as clean carboxylate salt (220 mg). The carboxylic salt (130 mg) was treated with acetic hydrazide (35 mg, 0.405 mmol) and phosphorus oxychloride (5 mL) then heated at 60° C. for 3 h. The solution was poured into cold saturated sodium bicarbonate (30 mL) in an ice bath and extracted with ethyl acetate (3×). The combined organic layers were dried over sodium sulfate and after concentration under reduced pressure, the crude material was purified by Analogix (dichloromethane/methanol) to give an off-white solid (60 mg, 43.3%).
MS (ESP): 528.0 (MH+) for C27H25N7O3S
1H NMR (300 MHz, CD3OD): δ 1.23 (t, 3H), 1.40 (d, 6H), 2.57 (s, 3H), 3.35 (q, 2H), 4.50 (q, 2H), 6.97 (d, 1H), 7.31 (m, 3H), 7.63 (d, 1H), 7.68 (d, 1H), 7.70 (d, 1H), 7.83 (s, 1H), 7.91 (s, 1H), 8.33 (d, 1H)
To a 100 mL round bottom flask was charged methyl 6-(3-ethylureido)-6′-isopropoxy-4-(4-(trifluoromethyl)thiazol-2-yl)-3,4′-bipyridine-2′-carboxylate (Intermediate 147, 450 mg) with ethanol (20 mL). Hydrazine monohydrate (6 mL) was added and the mixture heated to reflux for 1 h. After concentration under reduced pressure, the crude product was dried in a vacuum oven at 50° C. for 2 h. The residue was dissolved in tetrahydrofuran (30 mL), 1,1′-carbonyl diimidazole (0.53 g) was added and the mixture was stirred at room temperature for 3 h. Since starting material remained, another portion of 1,1′-carbonyl diimidazole (1 g) was added and the mixture was stirred for another 10 min. After concentration, the crude product was purified by prep. HPLC to give an off-white solid (130 mg)
MS (ESP): 536.1 (MH+) for C22H20F3N7O4S
1H NMR (300 MHz, CD3OD): 1.22 (t, 3H), 1.36 (d, 6H), 3.35 (q, 2H), 5.46 (m, 1H), 6.89 (s, 1H), 7.41 (s, 1H), 7.92 (s, 1H), 8.33 (s, 1H), 8.36 (s, 1H)
19F NMR (300 MHz, CD3OD): −65.92
To a vial was charged methyl 6-(3-ethylureido)-6′-isopropoxy-4-(4-(trifluoromethyl)thiazol-2-yl)-3,4′-bipyridine-2′-carboxylate (Intermediate 147, 450 mg), tetrahydrofuran (30 mL) and water (30 mL). Lithium hydroxide (0.8 g) was added and the resulting mixture was stirred at room temperature for 1 h. The reaction mixture was filtered, the solid was washed with methyl tert-butyl ether and determined to be by-products. The aqueous layer was diluted with water and extracted with methyl tert-butyl ether twice. The aqueous was acidified with 6 N HCl to pH 2-3, and extracted with ethyl acetate (3×). The combined ethyl acetate layers were dried over sodium sulfate and dried in a vacuum oven at 50° C. for overnight to give a yellow solid (190 mg) as clean carboxylic acid.
The carboxylic acid (180 mg, 0.364 mmol) was treated with acetic hydrazide (48 mg, 0.581 mmol) and phosphorus oxychloride (3 mL) then heated at 65° C. for 2 h. The excess phosphorus oxychloride was removed in vacuo and the residue quenched by saturated sodium bicarbonate (30 mL). The resulting mixture was extracted with ethyl acetate (3×). The organic layers were combined and dried over sodium sulfate. After concentration under reduced pressure, the crude mixture was purified by Analogix (dichloromethane/methanol) to give a yellow solid (52 mg, 26.8%)
MS (ESP): 534.3 (MH+) for C23H22F3N7O3S
1H NMR (300 MHz, CD3OD): 1.22 (t, 3H), 1.36 (d, 6H), 2.62 (s, 3H), 3.35 (q, 2H), 5.48 (m, 1H), 6.85 (d, 1H), 7.53 (d, 1H), 7.80 (s, 1H), 8.26 (d, 1H), 8.37 (d, 1H)
19F NMR (300 MHz, CD3OD): −65.94
To a 100 mL round bottom flask was charged methyl 6-(3-ethylureido)-6′-isopropoxy-4-(4-phenylthiazol-2-yl)-3,4′-bipyridine-2′-carboxylate (Intermediate 148, 500 mg) with anhydrous ethanol (20 mL). Hydrazine monohydrate (6 mL) was added and the mixture was heated to reflux for 2 h. After concentration the crude product was dried in a vacuum oven at 60° C. overnight.
The crude hydrazide was dissolved in tetrahydrofuran (30 mL), 1,1′-carbonyl diimidazole (660 mg) added, and the mixture was stirred at room temperature for 1 h. After concentration under reduced pressure, the crude product was purified by prep. HPLC to give a yellow solid (100 mg).
MS (ESP): 544.2 (MH+) for C27H25N7O4S
1H NMR (300 MHz, CD3OD): δ 1.23 (t, 3H), 1.35 (d, 6H), 3.35 (q, 2H), 5.46 (m, 1H), 6.92 (d, 1H), 7.34 (m, 2H), 7.46 (d, 1H), 7.58 (d, 1H), 7.72 (d, 1H), 7.75 (d, 1H), 7.93 (s, 1H), 8.02 (s, 1H), 8.29 (s, 1H)
To a vial was charged methyl 6-(3-ethylureido)-6′-isopropoxy-4-(4-phenylthiazol-2-yl)-3,4′-bipyridine-2′-carboxylate (Intermediate 148, 0.66 g), tetrahydrofuran (30 mL) and water (30 mL). Lithium hydroxide (1 g) was added and the resulting mixture was stirred at room temperature overnight. The reaction mixture was diluted with water and a cloudy mixture resulted. Filtration was applied to remove the solid and the filtrate was extracted with methyl tert-butyl ether (3×). The aqueous layer was acidified by 6 N HCl to pH 2-3, and extracted with ethyl acetate (3×). The combined ethyl acetate layers were dried over sodium sulfate, to give solid carboxylic acid (100 mg). The carboxylic acid (100 mg, 0.199 mmol) was treated with acetic hydrazide (25 mg, 0.298 mmol) and phosphorus oxychloride (5 mL) then heated at 60° C. for 3 h. The solution was poured into cold saturated sodium bicarbonate (30 mL) in an ice bath and extracted with ethyl acetate (3×). The combined organic layers were dried over sodium sulfate. After concentration, the crude mixture was purified by Analogix (dichloromethane/methanol) to give a white solid (50 mg, 46.5%).
MS (ESP): 542.1 (MH+) for C28H27N7O3S
1H NMR (300 MHz, CD3OD): δ 1.23 (t, 3H), 1.35 (d, 6H), 2.57 (s, 3H), 3.35 (q, 2H), 5.48 (m, 1H), 6.91 (d, 1H), 7.29 (m, 3H), 7.60 (d, 1H), 7.66 (s, 1H), 7.67 (s, 1H), 7.82 (s, 1H), 7.91 (s, 1H), 8.33 (d, 1H).
To a 100 mL round bottom flask was charged methyl 6′-(cyclopropylmethoxy)-6-(3-ethylureido)-4-(4-(trifluoromethyl)thiazol-2-yl)-3,4′-bipyridine-2′-carboxylate (Intermediate 149, 100 mg) with ethanol (20 mL). Hydrazine monohydrate (1.2 mL) was added and the mixture heated to reflux for 1 h. After concentrating the crude product was dried in a vacuum oven at 50° C. for 2 h.
The crude product was dissolved in anhydrous 1,4-dioxane (30 mL), 1,1′-carbonyl diimidazole (0.53 g) added and the mixture was stirred at room temperature for 3 h, starting material remained. Another portion of 1,1′-carbonyl diimidazole (0.4 g) was added, and the mixture was stirred for another 10 min. After concentration, the crude product was purified by Analogix (dichloromethane/methanol) to give an off-white solid (35 mg)
MS (ESP): 548.1 (MH+) for C23H20F3N7O4S
1H NMR (300 MHz, CD3OD): 0.37-0.41 (m, 2H), 0.58-0.61 (m, 2H), 1.23 (t, 3H), 1.20-1.30 (m, 1H), 3.35 (q, 2H), 4.24 (d, 2H), 6.88 (d, 1H), 7.32 (d, 1H), 7.80 (s, 1H), 8.26 (s, 1H), 8.36 (s, 1H)
19F NMR (300 MHz, CD3OD): −66.01
To a vial was charged methyl 6′-(cyclopropylmethoxy)-6-(3-ethylureido)-4-(4-(trifluoromethyl)thiazol-2-yl)-3,4′-bipyridine-2′-carboxylate (Intermediate 149), tetrahydrofuran (30 mL) and water (30 mL). Lithium hydroxide (0.5 g) was added and the resulting mixture was stirred at room temperature for 2 h. The mixture was extracted with ethyl acetate once then the aqueous layer acidified by 6 N HCl to pH 2-3. The resulting acidic solution was extracted with ethyl acetate (3×), the combined organic layers dried over sodium sulfate and concentrated. The crude carboxylic acid (450 mg) was treated with acetic hydrazide (70 mg, 0.945 mmol) and phosphorus oxychloride (4 mL). The mixture was heated at 65° C. for 3 hours, to give very impure product. The solution was poured into cold saturated sodium bicarbonate (30 mL) in an ice bath and extracted with ethyl acetate (3×). The organic layers was combined and dried over sodium sulfate. After concentration under reduced pressure, the crude mixture was purified by Analogix (dichloromethane/methanol) to give a light yellow solid (24 mg)
MS (ESP): 546.0 (MH+) for C24H22F3N7O3S
1H NMR (300 MHz, CD3OD): 0.37-0.41 (m, 2H), 0.58-0.61 (m, 2H), 1.23 (t, 3H), 1.20-1.30 (m, 1H), 3.35 (q, 2H), 4.24 (d, 2H), 6.88 (d, 1H), 7.55 (d, 1H), 7.81 (s, 1H), 8.26 (d, 1H), 8.38 (d, 1H).
19F NMR (300 MHz, CD3OD): −67.56
To a 100 mL round bottom flask was charged methyl 6′-(cyclopropylmethoxy)-6-(3-ethylureido)-4-(4-phenylthiazol-2-yl)-3,4′-bipyridine-2′-carboxylate (Intermediate 150, 600 mg) with anhydrous ethanol (20 mL). Hydrazine monohydrate (2.5 mL) was added and the mixture was heated to reflux for 2 h. After concentration under reduced pressure, the crude product was dried in a vacuum oven at 60° C. overnight.
The residue was dissolved in anhydrous 1,4-dioxane (30 mL), and 1,1′-carbonyl diimidazole (600 mg) was added, and the mixture was stirred at room temperature for 1 h. Another portion of 1,1′-carbonyl diimidazole (0.7 g) was added, and the reaction went to completion. After concentration under reduced pressure, the crude product was purified by prep. HPLC to give a white solid (15 mg).
MS (ESP): 556.2 (MH+) for C28H25N7O4S
1H NMR (300 MHz, DMSO-d6): δ 0.3-0.4 (m, 2H), 0.5-0.6 (m, 2H), 1.11 (t, 3H), 1.2-1.3 (m, 1H), 3.35 (q, 2H), 4.17 (d, 2H), 6.98 (s, 1H), 7.36-7.40 (m, 3H), 7.62 (s, 1H), 7.74-7.77 (m, 2H), 8.21 (s, 1H), 8.23 (d, 1H), 8.30 (s, 1H), 9.47 (s, 1H).
To a 100 mL round bottom flask was charged methyl 6-(3-ethylureido)-6′-morpholino-4-(4-(trifluoromethyl)thiazol-2-yl)-3,4′-bipyridine-2′-carboxylate (Intermediate 151, 150 mg, 0.28 mmol) with ethanol (20 mL). Hydrazine monohydrate (3 mL) was added and the mixture was heated to reflux for 0.5 h. While hot, the reaction mixture was filtered through a Celite pad to remove residual Pd catalyst from previous step. The filtrate was concentrated and dried in a vacuum oven at 50° C. for 2 h.
The crude was dissolved in tetrahydrofuran (30 mL), 1,1′-carbonyl diimidazole (0.2 g) added, and the mixture was stirred at room temperature for 2 h. Since starting material remained, another portion of 1,1′-carbonyl diimidazole (0.3 g) was added, and the mixture was stirred for another 1 h. After concentration under reduced pressure, the crude product was purified by Analogix, but the product still contained imidazole. The material was triturated by water to give an off-white solid (60 mg, 38.2%)
MS (ESP): 563.1 (MH+) for C23H21F3N8O4S
1H NMR (300 MHz, DMSO-d6): 1.10 (t, 3H), 3.35 (q, 2H), 3.52-3.56 (m, 4H), 3.64-3.70 (m, 4H), 7.01 (d, 2H), 7.56 (m, 1H), 8.18 (s, 1H), 8.36 (s, 1H), 8.58 (d, 1H), 9.51 (s, 1H), 12.7 (m, 1H)
19F NMR (300 MHz, DMSO-d6): −65.76
To a vial was charged methyl 6-(3-ethylureido)-6′-morpholino-4-(4-(trifluoromethyl)thiazol-2-yl)-3,4′-bipyridine-2′-carboxylate (Intermediate 151, 200 mg, 0.373 mmol), tetrahydrofuran (30 mL) and water (10 mL). Lithium hydroxide (0.5 g) was added, and the resulting mixture was stirred at room temperature for 1 h. The mixture was diluted with water and extracted with ethyl acetate once. The aqueous layer was acidified by 6 N HCl to pH 2-3, and extracted with ethyl acetate (3×). The combined organic layers were dried over sodium sulfate and after concentration dried in a vacuum oven at 50° C. overnight to give a yellow solid (120 mg, 61.5%).
The carboxylic acid (110 mg, 0.21 mmol) was treated with acetic hydrazide (26 mg, 0.32 mmol) and phosphorus oxychloride (3 mL) then heated at 60° C. for 2 h. The solution was poured into cold saturated sodium bicarbonate in an ice bath. The resulting mixture was extracted with ethyl acetate (3×). The organic layers were combined and dried over sodium sulfate. After concentration under reduced pressure, the crude mixture was purified by Analogix (dichloromethane/methanol) to give a yellow solid (41 mg, 34.9%)
MS (ESP): 561.3 (MH+) for C24H23F3N8O3S
1H NMR (300 MHz, CD3OD): 1.22 (t, 3H), 2.61 (s, 3H), 3.34 (q, 2H), 3.60 (t, 4H), 3.77 (t, 4H), 6.92 (d, 1H), 7.30 (d, 1H), 7.82 (s, 1H), 8.25 (d, 1H), 8.36 (d, 1H)
19F NMR (300 MHz, CD3OD): −65.79
To a 100 mL round bottom flask was charged methyl 6-(3-ethylureido)-6′-morpholino-4-(4-phenylthiazol-2-yl)-3,4′-bipyridine-2′-carboxylate (Intermediate 152, 350 mg) with anhydrous ethanol (50 mL). Hydrazine monohydrate (2 mL) was added and the mixture was heated to reflux for 1 hour. After concentration under reduced pressure, the crude product was dried in a vacuum oven at 60° C. overnight.
The crude residue was dissolved in tetrahydrofuran (30 mL), 1,1′-carbonyl diimidazole (600 mg) added, and the mixture was stirred at room temperature for 1 h. After concentration under reduced pressure, the crude product was purified by Analogix (dichloromethane/methanol) to give a white solid (62 mg).
MS (ESP): 571.2 (MH+) for C28H26N8O4S
1H NMR (300 MHz, CD3OD): δ 1.11 (t, 3H), 3.22 (q, 2H), 3.50 (t, 4H), 3.65 (t, 4H), 6.97 (s, 1H), 7.10 (d, 2H), 7.36-7.45 (m, 3H), 7.67 (br, 1H), 7.83 (d, 1H), 7.85 (d, 1H), 8.22 (s, 1H), 8.24 (s, 1H), 8.29 (d, 1H), 9.48 (s, 1H)
To a vial was charged methyl 6-(3-ethylureido)-6′-morpholino-4-(4-phenylthiazol-2-yl)-3,4′-bipyridine-2′-carboxylate (Intermediate 152, 0.34 g), tetrahydrofuran (30 mL) and water (30 mL). Lithium hydroxide (300 mg) was added, and the resulting mixture was stirred at room temperature overnight. The mixture was diluted with water and extracted with ethyl acetate once. The aqueous layer was then acidified to pH 2-3, and extracted with ethyl acetate (3×). The combined organic layers were dried over sodium sulfate, and after concentration, the resulting solid (acid) was used without further purification (100 mg).
The carboxylic acid (80 mg, 0.151 mmol) was treated with acetic hydrazide (25 mg, 0.305 mmol) and phosphorus oxychloride (3 mL) then heated at 60° C. for 4 h. The solution was poured into cold saturated sodium bicarbonate (30 mL) in an ice bath and extracted with ethyl acetate (3×). The combined organic layers were dried over sodium sulfate. After concentration, the crude mixture was purified by Analogix (dichloromethane/methanol) to give an off-white solid (25 mg).
MS (ESP): 569.1 (MH+) for C29H28N8O3S
1H NMR (300 MHz, CD3OD): δ ppm 1.23 (t, 3H), 2.57 (s, 3H), 3.35 (q, 2H), 3.57 (t, 4H), 3.71 (t, 4H), 6.94 (s, 1H), 7.33-7.39 (m, 4H), 7.75 (d, 1H), 7.78 (d, 1H), 7.82 (s, 1H), 7.90 (s, 1H), 8.35 (d, 1H)
To a 100 mL round bottom flask was charged methyl 6-(3-ethylureido)-6′-(1-methylpiperidin-4-yloxy)-4-(4-(trifluoromethyl)thiazol-2-yl)-3,4′-bipyridine-2′-carboxylate (Intermediate 153, 100 mg, 0.213 mmol) with ethanol (20 mL). Hydrazine monohydrate (0.2 mL) was added and the mixture heated to reflux for overnight. The reaction was concentrated and dried in a vacuum oven at 40° C. for 2 h.
The crude product was dissolved in anhydrous tetrahydrofuran (10 mL), 1,1′-carbonyl diimidazole (80 mg) added, and the mixture was stirred at room temperature for 1 h. After concentration, the crude product was triturated with water to give an off-white solid (56 mg, 53.8% in two steps)
MS (ESP): 563.1 (MH+) for C25H25F3N8O4S
1H NMR (300 MHz, DMSO-d6): 1.10 (t, 3H), 1.67-1.80 (m, 2H), 1.98-2.05 (m, 2H), 2.20 (s, 3H), 2.15-2.30 (m, 2H), 2.60-2.70 (m, 2H), 3.16-3.25 (m, 2H), 4.03 (br, 1H), 5.06 (m, 1H), 6.93 (d, 1H), 7.30 (d, 1H), 7.52 (s, 1H), 8.15 (d, 1H), 8.36 (s, 1H), 8.60 (d, 1H), 9.51 (s, 1H)
19F NMR (300 MHz, DMSO-d6): −62.91
To a vial was charged methyl 6-(3-ethylureido)-6′-(1-methylpiperidin-4-yloxy)-4-(4-(trifluoromethyl)thiazol-2-yl)-3,4′-bipyridine-2′-carboxylate (Intermediate 153, 150 mg, 0.266 mmol), tetrahydrofuran (30 mL), sodium hydroxide (24 wt % in water, 0.5 mL) and the resulting mixture was stirred at room temperature for overnight. The mixture was concentrated to dryness and the crude salt used for the cyclization.
The carboxylic salt was treated with acetic hydrazide (37 mg, 0.449 mmol) and phosphorus oxychloride (4 mL) then heated at 65° C. for 1 h. The reaction went to completion based on LC, and the solution was poured into cold saturated sodium bicarbonate in an ice bath and extracted with ethanol/tetrahydrofuran (1:1) three times. The organic layers were combined and dried over sodium sulfate. After concentration, the crude mixture was purified by Analogix (dichloromethane/methanol) to give a light yellow solid (35 mg, 22.4%)
MS (ESP): 589.2 (MH+) for C26H27F3N8O3S
1H NMR (300 MHz, DMSO-d6): 1.18 (t, 3H), 1.9-2.1 (br, 2H), 2.2-2.3 (br, 2H), 2.59 (s, 3H), 2.6-2.8 (br, 2H), 3.05 (q, 2H), 3.6-3.8 (br, 2H), 5.2-5.3 (br, 1H), 7.06 (s, 1H), 7.56 (br, 2H), 8.20 (s, 1H), 8.40 (s, 1H), 8.62 (s, 1H), 9.57 (s, 1H)
19F NMR (300 MHz, DMSO-d6): −62.97
To a 100 mL round bottom flask was charged methyl 6′-(2-(dimethylamino)ethoxy)-6-(3-ethylureido)-4-(4-(trifluoromethyl)thiazol-2-yl)-3,4′-bipyridine-2′-carboxylate (Intermediate 154, 100 mg, 0.185 mmol) with of ethanol (20 mL). Hydrazine monohydrate (0.4 mL) was added and the mixture was heated to reflux for overnight. While hot, the reaction was filtered through a Celite pad to remove residual Pd catalyst and the filtrate was concentrated to dryness.
The crude product was dissolved in anhydrous tetrahydrofuran (10 mL), 1,1′-carbonyl diimidazole (110 mg) was added, and the mixture was stirred at room temperature for overnight. After concentration, the brown oily solid was triturated with water to give a light brown solid (50 mg, 47.6% in two steps)
MS (ESP): 565.2 (MH+) for C23H23F3N8O4S
1H NMR (300 MHz, DMSO-d6): 1.10 (t, 3H), 2.22 (s, 6H), 2.65 (t, 2H), 3.20 (m, 2H), 4.42 (t, 2H), 6.99 (d, 1H), 7.32 (d, 1H), 7.54 (t, br, 1H), 7.62-7.70 (m, 1H), 8.15 (d, 1H), 8.36 (s, 1H), 8.60 (d, 1H), 9.53 (s, 1H)
19F NMR (DMSO-d6): −62.90
Methyl 6′-(2-(dimethylamino)ethoxy)-6-(3-ethylureido)-4-(4-(trifluoromethyl)thiazol-2-yl)-3,4′-bipyridine-2′-carboxylate (Intermediate 154, 500 mg) was treated with acetic hydrazide (100 mg, 1.21 mmol) and phosphorus oxychloride (5 mL) then heated at 65° C. for 1 h. After cooling the solution was poured into cold saturated sodium bicarbonate in an ice bath. The resulting mixture was extracted with ethanol/tetrahydrofuran (1:1) three times. The organic layers was combined and dried over sodium sulfate. After concentration, the crude mixture was purified by prep. HPLC
MS (ESP): 563.1 (MH+) for C24H25F3N8O3S
6-(3-ethylureido)-4-(4-phenylthiazol-2-yl)pyridin-3-ylboronic acid (0.100 g, 0.27 mmol, Intermediate 16), 2-(5-bromopyridin-3-yl)-5-methyl-1,3,4-oxadiazole (0.111 g, 0.46 mmol, Intermediate 418), cesium carbonate (0.150 g, 0.46 mmol), dicyclohexyl(2′,4′,6′-triisopropylbiphenyl-2-yl)phosphine (XPhos) (0.039 g, 0.08 mmol) and tris(dibenzylideneacetone)dipalladium(0) (0.025 g, 0.03 mmol) were combined in dioxane (2.00 mL)/water (0.50 mL) and heated to 100° C. The solution was cooled to room temperature and the reaction mixture was diluted with ethyl acetate and washed twice with water, once with saturated sodium bicarbonate and brine. The combined organic extracts were dried over magnesium sulfate, filtered and evaporated to a yellow solid. Isco column (0%-100% ethyl acetate/dichloromethane) afforded the desired compound as a white solid 0.106 g, 81% yield.
MS (ESP): 484 (M+H+) for C23H22F3N7O4S.
1H NMR (DMSO-d6): δ 1.12 (t, 3H), 2.57 (s, 3H), 3.22 (q, 2H), 7.33 (q, 3H), 7.63 (m, 1H), 7.70 (d, 1H), 8.23 (s, 1H), 8.28 (s, 1H), 8.36 (s, 2H), 8.74 (s, 1H), 9.17 (s, 1H), 9.50 (s, 1H)
The following compounds have been synthesized as described for Example 10 from the starting materials indicated in the table below.
To a solution of 1-ethyl-3-(2′-(hydrazinecarbonyl)-4-(4-phenylthiazol-2-yl)-3,4′-bipyridin-6-yl)urea (0.036 g, 0.08 mmol, Intermediate 155) in THF (2.5 mL) and 1,1,1-trimethoxyethane (5 mL, 0.08 mmol) was added HCl (2.380 μL, 0.08 mmol) and the reaction was stirred at 120° C. DBU (0.118 mL, 0.78 mmol) was added and heating was continued. The reaction mixture was cooled to room temperature and concentrated to a red oil. Isco column (0%-10% methanol/dichloromethane) yielded pure product as a white solid 0.031 g, 82% yield.
MS (ESP): 484 (M+H+) for C25H21N7O2S.
1H NMR (DMSO-d6): δ 1.11 (t, 3H), 2.59 (s, 3H), 3.22 (q, 2H), 7.33 (q, 3H), 7.63 (dd, 4H), 8.11 (s, 1H), 8.22 (d, 1H), 8.36 (s, 1H), 8.75 (d, 1H), 9.53 (s, 1H).
The following compounds have been synthesized as described for Example 96 from the starting materials indicated in the table below.
The 1-ethyl-3-(5′-(hydrazinecarbonyl)-2′-(2-(4-methylpiperazin-1-yl)ethoxy)-4-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridin-6-yl)urea (Intermediate 165, 142 mg, 0.24 mmol) was dissolved in THF (2.4 mL) and cooled to 0° C. Diisopropylethylamine (46.0 μl, 0.26 mmol) was added dropwise, followed by the addition of 1,1′-carbonyldiimidazole (42.8 mg, 0.26 mmol). The ice bath was then removed and the mixture was stirred at RT for 3 h. The mixture was conc in vacuo and purified by silica gel chromatography (5-10% MeOH/CH2Cl2+1% NH4OH) to give 16.6 mg (11%) of the title compound.
LC/MS (ES+)[(M+H)+]: 620 for C26H28F3N9O4S
1H NMR (DMSO-d6): δ 9.47 (s, 1H); 8.65 (m, 1H); 8.54 (m, 1H); 8.25 (d, 2H); 8.14 (m, 1H); 7.61 (m, 1H); 4.15 (t, 2H); 3.21 (m, 2H); 2.18 (m, 10H); 2.07 (s, 3H); 1.10 (t, 3H).
The following compounds have been synthesized as described for Example 99 from the starting materials indicated in the table below.
The 6-(3-ethylureido)-4-(4-(pyridin-2-yl)thiazol-2-yl)pyridin-3-ylboronic acid (Intermediate 174, 0.076 g, 0.21 mmol), 2-(5-bromopyridin-3-yl)-5-methyl-1,3,4-oxadiazole (Intermediate 418, 0.059 g, 0.25 mmol), tetrakis(triphenylphosphine)palladium (0) (0.024 g, 0.02 mmol) and cesium carbonate (0.101 g, 0.31 mmol) were placed in a microwave vessel. The vessel was degassed and purged with N2 several times. Acetonitrile (2.5 ml) and water (0.625 ml) were added and the vessel was degassed and purged with N2 again. The vessel was heated in the microwave at 100° C. for 2 h. The mixture was then conc in vacuo. Acetonitrile was added and the resultant precipitate was collected and washed with acetonitrile and water. Purification by silica gel chromatography (0-10% MeOH/CH2Cl2) gave 0.017 g (17%) of the title compound.
LC/MS (ES+)[(M+H)+]: 485 for C24H20N8O2S
1H NMR (DMSO-d6): δ 9.51 (s, 1H); 9.18 (d, 1H); 8.76 (d, 1H); 8.59 (m, 1H); 8.38 (m, 3H); 8.30 (s, 1H); 7.81 (m, 1H); 7.65 (m, 2H); 7.35 (m, 1H); 3.23 (m, 2H); 2.57 (s, 3H); 1.12 (t, 3H).
Following the procedure for Example 104, 6-(3-ethylureido)-4-(4-(pyridin-2-yl)thiazol-2-yl)pyridin-3-ylboronic acid (Intermediate 174, 0.076 g, 0.21 mmol) and 5-bromopyridine-3-sulfonamide (0.073 g, 0.31 mmol) were reacted in the microwave at 100° C. for 1 h. The mixture was then conc in vacuo. Acetonitrile was added and the resultant precipitate was collected and washed with acetonitrile and water to give 0.016 g (16%) of the title compound.
LC/MS (ES+)[(M+H)+]: 482 for C21H19N7O3S2
1H NMR (DMSO-d6): δ 9.51 (s, 1H); 8.99 (m, 1H); 8.74 (m, 1H); 8.60 (m, 1H); 8.37 (s, 1H); 8.31 (m, 2H); 8.20 (m, 1H); 7.84 (m, 1H); 7.63 (m, 4H); 7.36 (m, 1H); 3.22 (m, 2H); 1.12 (t, 3H).
A solution of 1-ethyl-3-(2′-(hydrazinecarbonyl)-4-(4-(pyridin-2-yl)thiazol-2-yl)-3,4′-bipyridin-6-yl)urea (Intermediate 178, 56.4 mg, 0.12 mmol) in DMF (1 mL) was treated with diisopropylethylamine (0.03 mL, 0.18 mmol) and 1,1′-carbonyldiimidazole (29.8 mg, 0.18 mmol). The mixture was stirred at RT for 2 h. Methanol was added and the mixture was conc in vacuo. Purification by silica gel chromatography (0-10% MeOH/CH2Cl2) gave 15 mg (25%) of the title compound.
LC/MS (ES+)[(M+H)+]: 487 for C23H18N8O3S
1H NMR (500 MHz, CDCl3): δ 12.77 (br s, 1H); 9.52 (s, 1H); 8.73 (d, 1H); 8.61 (m, 1H); 8.39 (s, 1H); 8.36 (s, 1H); 8.24 (s, 1H); 7.92 (s, 1H); 7.82 (m, 1H); 7.59 (m, 3H); 7.36 (m, 1H); 3.23 (m, 2H); 1.13 (t, 3H).
The 1-(4-chloro-5′-(5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)-3,3′-bipyridin-6-yl)-3-ethylurea (Intermediate 183, 0.065 g, 0.18 mmol) and cesium carbonate (0.117 g, 0.36 mmol) were placed in a microwave vessel. The vessel was degassed and purged with N2. Tetrakis (triphenylphosphine)palladium (0) (0.021 g, 0.02 mmol) was added and the vessel was degassed and purged with N2. The 1-isobutyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole (0.10 mL, 0.40 mmol) was added, followed by dioxane (1.6 mL) and water (0.4 mL). The vessel was degassed and purged with N2 twice. The vessel was placed in the microwave for 2 h at 100° C. Purification by silica gel chromatography (0-10% MeOH/CH2Cl2) gave 0.017 g (21%) of the title compound.
LC/MS (ES+)[(M+H)+]: 449 for C22H24N8O3
1H NMR (DMSO-d6): δ 12.79 (s, 1H); 9.28 (s, 1H); 8.94 (m, 1H); 8.61 (m, 1H); 8.19 (s, 1H); 7.90 (m, 2H); 7.60 (s, 1H); 7.43 (s, 1H); 7.27 (s, 1H); 3.82 (d, 2H); 3.20 (m, 2H); 1.96 (m, 1H); 1.10 (t, 3H); 0.71 (s, 3H); 0.69 (s, 3H).
Diisopropylethylamine (0.058 mL, 0.33 mmol) was added to a solution of 1-ethyl-3-(5′-(hydrazinecarbonyl)-4-(4-morpholinophenyl)-3,3′-bipyridin-6-yl)urea (Intermediate 185, 0.102 g, 0.22 mmol) in DMF (2 mL). 1,1′-Carbonyldiimidazole (0.054 g, 0.33 mmol) was added in one portion and the resultant mixture was stirred at RT overnight. Purification by silica gel chromatography (0-10% MeOH/CH2Cl2) gave 0.066 g (62%) of the title compound.
LC/MS (ES+)[(M+H)+]: 488 for C25H25N7O4
1H NMR (DMSO-d6): δ 12.77 (s, 1H); 9.36 (s, 1H); 8.82 (m, 1H); 8.39 (m, 1H); 8.26 (s, 1H); 7.95 (m, 2H); 7.49 (s, 1H); 7.01 (m, 2H); 6.89 (m, 2H); 3.70 (m, 4H); 3.21 (m, 2H); 3.11 (m, 4H); 1.10 (t, 3H).
To a solution of tert-butyl 4-({6′-[(ethylcarbamoyl)amino]-5-(5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)-4′-[4-(trifluoromethyl)-1,3-thiazol-2-yl]-3,3′-bipyridin-2-yl}oxy)piperidine-1-carboxylate (Intermediate 191, 170 mg, 0.25 mmol) in dichloromethane (10 mL), trifluoroacetic acid (0.1 mL, 1.25 mmol) was added and stirred for 3 h at room temperature. Dichloromethane was evaporated from the reaction mixture, pH was adjusted to 8 with saturated sodium bicarbonate solution to obtain solid compound which was filtered and dried to afford 45 mg (31%) of 1-Ethyl-3-{5′-(5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)-2′-(piperidin-4-yloxy)-4-[4-(trifluoromethyl)-1,3-thiazol-2-yl]-3,3′-bipyridin-6-yl}urea.
1H NMR (400 MHz, CDCl3): δ 1.11 (m, 5H), 1.56 (br, 2H), 2.50 (m, 4H), 4.99 (m, 1H), 7.59 (m, 1H), 8.10 (m, 1H), 8.22-8.26 (m, 2H), 8.51-8.56 (m., 2H), 9.44 (s, 1H).
LC-MS: m/z 575.3 (M+H).
Tert-butyl 4-({6′-[(ethylcarbamoyl)amino]-5-(5-methyl-1,3,4-oxadiazol-2-yl)-4′-[4-(trifluoromethyl)-1,3-thiazol-2-yl]-3,3′-bipyridin-2-yl}oxy)piperidine-1-carboxylate (Intermediate 192, 150 mg, 0.22 mmol) was dissolved in dichloromethane (10 mL), trifluoroacetic acid (0.3 mL, 1.1 mM) was added and stirred for 3 h at room temperature. Dichloromethane was evaporated from the reaction mixture, pH was adjusted to 8 with saturated sodium bicarbonate solution to yield solid compound which was filtered and dried to afford 60 mg (47%) of 1-Ethyl-3-{5′-(5-methyl-1,3,4-oxadiazol-2-yl)-2′-(piperidin-4-yloxy)-4-[4-(trifluoromethyl)-1,3-thiazol-2-yl]-3,3′-bipyridin-6-yl}urea.
1H NMR (400 MHz, CD3OD): δ 1.34 (m, 5H), 1.76 (m, 3H), 2.62 (t, 3H), 2.72 (m, 5H), 4.28 (q, 2H), 5.21 (m, 1H), 8.21 (m, 1H), 8.29 (m, 2H), 8.58 (s, 1H), 8.85 (d, 1H)
LC-MS: m/z 576.2 (M+H)
To a stirred solution of 3-({6′-[(ethylcarbamoyl)amino]-5-(hydrazinylcarbonyl)-4′-[4-(trifluoromethyl)-1,3-thiazol-2-yl]-3,3′-bipyridin-2-yl}oxy)propanoic acid (Intermediate 196, 240 mg, 0.44 mmol) in tetrahydrofuran (15 mL) which was cooled to 0° C., phosgene (66 mg, 0.66 mmol) (slowly added to the reaction mixture at 0° C. The reaction mixture was maintained at room temperature for 3 h. The solvent was distilled completely under reduced pressure to give crude product which was washed with diethyl ether and pentane and purified by reverse phase preparative HPLC to afford 45 mg (18%) of 3-({6′-[(ethylcarbamoyl)amino]-5-(5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)-4′-[4-(trifluoromethyl)-1,3-thiazol-2-yl]-3,3′-bipyridin-2-yl}oxy)propanoic acid.
1H NMR (400 MHz, CD3OD): δ 1.2.0-1.24 (t, 3H), 2.69 (br, 4H), 3.36 (m, 3H), 4.17 (br s, 2H), 7.789 (d, 1H), 7.98 (d, 1H), 8.19 (d, 1H), 8.26 (s, 1H), 8.39 (s, 2H).
LC-MS: m/z 566.3 (M+H).
To a stirred solution of 1-Ethyl-3-{5′-(hydrazinylcarbonyl)-2′-(tetrahydro-2H-pyran-4-ylmethoxy)-4-[4-(trifluoromethyl)-1,3-thiazol-2-yl]-3,3′-bipyridin-6-yl}urea (Intermediate 199, 0.4 g, 0.70 mmol) in tetrahydrofuran (10 mL) which was cooled to 0° C., phosgene (0.1 g, 1.06 mmol) was slowly added to the reaction mixture at 0° C. The reaction mixture was maintained at room temperature for 3 h. The solvent was distilled off completely under reduced pressure to get crude compound which was washed with diethyl ether and pentane to afford 200 mg (48%) of 1-ethyl-3-{5′-(5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)-2′-(tetrahydro-2H-pyran-4-ylmethoxy)-4-[4-(trifluoromethyl)-1,3-thiazol-2-yl]-3,3′-bipyridin-6-yl}urea.
1H NMR (400 MHz, DMSO-d6): δ 0.91-1.23 (m, 4H), 1.55 (br, 1H), 1.76 (s, 1H), 1.90-1.92 (d, 1H), 2.08 (s, 1H), 3.08-3.14 (m, 2H), 3.19-3.22 (m, 2H), 3.67-3.69 (dd, 2H), 3.91-3.93 (d, 2H), 7.61 (br, 1H), 8.15 (d, 1H), 8.26-8.32 (m, 2H), 8.66-8.67 (d, 1H), 9.47-9.48 (d, 1H)
LC-MS: m/z 592.3 (M+2).
1-Ethyl-3-{5′-(hydrazinylcarbonyl)-2′-(tetrahydro-2H-pyran-4-ylmethoxy)-4-[4-(trifluoromethyl)-1,3-thiazol-2-yl]-3,3′-bipyridin-6-yl}urea (Intermediate 199, 400 mg, 1.7 mmol) was taken in triethylorthoacetate (5 mL) and the reaction mixture was heated to 120° C. for 12 h. The reaction mixture was cooled to room temperature, the solvent was distilled completely under reduced pressure to give crude product which was washed with diethyl ether and pentane to afford 150 mg 36.5% 1-ethyl-3-{5′-(5-methyl-1,3,4-oxadiazol-2-yl)-2′-(tetrahydro-2H-pyran-4-ylmethoxy)-4-[4-trifluoromethyl)-1,3-thiazol-2-yl]-3,3′-bipyridin-6-yl}urea as solid.
1H NMR (400 MHz, DMSO-d6): δ 1.09-1.13 (m, 2H), 1.31 (br, 2H), 1.37-1.56 (t, 3H), 1.69 (br, 1H), 2.63 (s, 3H), 3.23-3.29 (t, 2H), 3.84-3.87 (dd, 2H), 3.98-4.00 (d, 2H), 4.29-4.34 (q, 2H), 7.71 (s, 2H), 8.20 (d, 1H), 8.26 (s, 1H), 8.64 (s, 1H), 8.85 (d, 1H)
LC-MS: m/z 591 (M+2).
The following Examples were prepared according to the general procedure described below from the starting material indicated in the Table.
A suspension of corresponding carboxylic acid (0.3 mmol), hydrazine acetate (0.9 mmol) in phosphorus oxychloride (2.5 mL) was heated at 70° C. for 2 h. The solution was then cooled and concentrated to dryness. A solution of saturated potassium carbonate was added to the crude and extracted with ethyl acetate (3×). The combined organic layers were washed with brine and dried over sodium sulfate. The solvent was removed under vacuum and the crude product was purified by Analogix using dichloromethane-methanol.
The following Examples were prepared as described in the general procedure from the starting materials indicated in the Table.
A suspension of the corresponding hydrazide (0.3 mmol) in anhydrous tetrahydrofuran (2 mL) was treated with triethyl amine (0.6 mmol) and 1,1′-carbonyl diimidazole (0.12 mmol). The reaction was stirred at room temperature for 12 h, concentrated to dryness and purified directly by Analogix using dichloromethane-methanol to give (˜50%) product as an off-white solid.
A suspension of (S)-tert-butyl 1-(5-(2-(2-(diethylamino)ethoxy)-6′-(3-ethylureido)-4′-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridin-5-yl)-1,3,4-oxadiazol-2-yl)-2-methylpropylcarbamate (Intermediate 212, 0.2 mmol) in methanol (1 mL) was treated with HCl in 1,4-dioxane (4N, 2 mL) at room temperature for 6 h. The solution was then concentrated to dryness to give an off-white solid (80%).
MS (ESP): 648 (MH+) for C29H37ClF3N9O3S
1H NMR (300 MHz, CD3OD): δ 1.06-1.28 (m, 15H), 2.48 (m, 2H), 2.65 (m, 1H), 3.10-3.11 (m, 4H), 3.31-3.32 (m, 2H), 3.73 (m, 1H), 4.76 (m, 2H), 8.01 (m, 1H), 8.35 (m, 1H), 8.40 (m, 1H), 8.44-8.45 (m, 1H), 9.01 (m, 1H)
19F NMR (300 MHz, CD3OD): δ −65.81
A suspension of 2-(2-(diisopropylamino)ethoxy)-6′-(3-propylureido)-4′-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridine-5-carboxylic acid (Intermediate 220, 0.3 mmol), and hydrazine acetate (0.9 mmol) in phosphorus oxychloride (2.5 mL) was heated at 70° C. for 2 h. The solution was then cooled and concentrated to dryness. A solution of saturated potassium carbonate was added to the crude and product was extracted with ethyl acetate (3×). The combined organic layers were washed with brine and dried over sodium sulfate. All solvents were removed under vacuum and the crude was purified by Analogix using dichloromethane-methanol.
MS (ESP): 633.3 (M+H+) for C29H35F3N8O3S
1H NMR (300 MHz, CD3OD): δ 0.95 (m, 12H), 0.99 (m, 3H), 1.64-1.66 (m, 2H), 2.35-2.40 (m, 2H) 2.62 9 (s, 3H), 2.88-2.92 (m, 2H), 3.27 (m, 2H), 4.02-4.06 (m, 2H), 7.84 (s, 1H), 8.27 (s, 1H), 8.29-8.30 (m, 2H), 8.83-8.84 (m, 1H).
19F NMR (300 MHz, CD3OD): δ 65.92
A suspension of 1-(2′-(2-(diisopropylamino)ethoxy)-5′-(5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)-4-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridin-6-yl)-3-propylurea (Intermediate 221, 0.3 mmol) in anhydrous tetrahydrofuran (2 mL) was treated with triethyl amine (0.6 mmol) and 1,1′-carbonyl diimidazole (0.12 mmol). The reaction was stirred at room temperature for 12 h, concentrated to dryness and purified by Analogix chromatography using dichloromethane-methanol to give (50%) of an off-white solid.
MS (ESP): 635.1 (MH+) for C28H33F3N8O4S
1H NMR (300 MHz, DMSO-d6): δ 0.81-0.88 (m, 12H), 0.90-0.93 (m, 3H), 1.51 (m, 2H), 2.16-2.18 (m, 2H), 2.82-2.84 (m, 2H), 3.14-3.18 (m, 2H), 3.84-3.86 (m, 2H), 7.01 (m, 1H), 7.63 (m, 1H), 8.02-8.02 (m, 1H) 8.21-8.25 (m, 2H), 8.48-8.51 (m, 2H), 9.43 (m, 1H)
19F NMR (300 MHz, DMSO-d6): δ −62.97
The following compounds have been synthesized as described for Example 21 from the starting materials indicated in the table below.
1-(5′-Bromo-4-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridin-6-yl)-3-ethylurea (Example 21, 100 mg, 0.21 mmol), 2,4-dioxo-1,2,3,4-tetrahydropyrimidin-5-ylboronic acid (49.5 mg, 0.32 mmol), tris(dibenzylideneacetone)dipalladium(0) (19.39 mg, 0.02 mmol), 2-dicyclohexylphosphino-2′,4′,6′-tri-iso-propyl-1,1′-biphenyl (30.3 mg, 0.06 mmol) and sodium carbonate were taken in a round bottomed flask. It was degassed with nitrogen and 5 mL of dioxane:water (4:1) was added and degassed again. The resulting mixture was heated at 100° C. for 40 min, then the reaction mixture was filtered. The filtrate was concentrated under reduced pressure and the resulting residue was partitioned between water and 3% MeOH in dichloromethane. The layers were separated and the aqueous was back extracted with the solvent three times. The extracts were combined, washed with water and brine and dried over magnesium sulfate, then concentrated under reduced pressure and purified by reverse phase HPLC to give a white solid (62 mg).
MS (ESP): 504 (M+1) for C21H16F3N7O3S
1H-NMR (DMSO-d6) δ: 1.10 (t, 3H); 3.01-3.48 (m, 2H); 7.57 (br s, 1H); 7.92 (d, 1H); 8.12 (s, 1H); 8.25 (s, 1H); 8.36 (s, 1H); 8.45 (d, 1H); 8.57 (s, 1H); 8.92 (d, 1H); 9.49 (s, 1H): 11.42 (brs, 2H).
The following compounds have been synthesized as described for Example 131 from the starting materials indicated in the table below.
To a mixture of 1-(5′-(5-amino-1,3,4-oxadiazol-2-yl)-4-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridin-6-yl)-3-ethylurea (Example 136, 70 mg, 0.15 mmol) in methanol (4 mL), potassium hydroxide (16.49 mg, 0.29 mmol) was added and heated at 70° C. for 20 h. The reaction mixture was cooled to room temperature, concentrated under reduced pressure, and the resulting residue was taken in conc. hydrochloric acid (3 mL) and heated at 80° C. for another 1 h. The reactiom mixture was cooled to room temperature and neutralized with 10 N sodium hydroxide solution. The solid that precipitated was collected by filtration, dried, and purified by reverse phase HPLC.
MS (ESP): 477 (M+1) for C19H15F3N8O2S
1H-NMR (DMSO-d6) δ: 1.10 (t, 3H); 3.14-3.28 (m, 2H); 7.55 (brs, 1H); 8.10 (t, 1H); 8.25 (s, 1H); 8.36 (s, 1H); 8.56 (s, 2H); 9.00 (s, 1H); 9.51 (s, 1H); 11.89 (s, 1H); 12.17 (s, 1H)
To a mixture of 1-ethyl-3-(5′-(hydrazinecarbonyl)-4-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridin-6-yl)urea (Intermediate 9, 138 mg, 0.31 mmol) in 1,4-dioxane (3 mL), sodium bicarbonate (25.7 mg, 0.31 mmol) in water (1 mL) was added and the mixture was stirred for 5 min at room temperature. Cyanic bromide (0.122 mL, 0.37 mmol) (3M sol. in DCM) was added to the reactiom mixture and stirred at room temperature for 1 h. The product was precipitated with water, collected by filtration and dried to give a light yellow solid (101 mg).
MS (ESP): 477 (M+1) for C19H15F3N8O2S
1H-NMR (DMSO-d6) δ: 1.11 (t, 3H); 3.14-3.28 (m, 2H); 7.43 (brs, 2H); 7.56 (brs, 1H); 8.08 (t, 1H); 8.24 (s, 1H); 8.38 (s, 1H); 8.56 (s, 1H); 8.61 (d, 1H); 9.00 (d, 1H); 9.51 (s, 1H).
1-Ethyl-3-(5-(5-(hydrazinecarbonyl)-4-(1-methyl-1H-1,2,4-triazol-5-yl)thiazol-2-yl)-4-(4-(trifluoromethyl)thiazol-2-yl)pyridin-2-yl)urea (Intermediate 234, 70 mg, 0.13 mmol) was taken in 1,1,1-trimethoxyethane (2 mL, 0.13 mmol) and a drop of HCl was added to it. The mixture was refluxed at 120° C. for 25 min, then DMF (2 mL) and DBU (4-8 drops) were added and the mixture was refluxed for 20 h at 100° C. The reaction mixture was cooled to room temperature and water was added to precipitate the product. The product was collected via filtration and washed with 1:1 water and acetonitrile. The filtrate was extracted with ethyl acetate three times. The combined extracts were washed with water and brine, dried over magnesium sulfate and concentrated. The crude was combined with the precipitated product and purified by normal phase chromatography (2% MeOH in DCM to 6% MeOH in DCM). The fractions containing the product were combined and concentrated to give off-white solid (20 mg).
MS (ESP): 563 (M+1) for C21H17F3N10O2S2
1H-NMR (DMSO-d6) δ: 1.11 (t, 3H); 2.50 (s, 3H); 3.13-3.27 (m, 2H); 3.80 (s, 3H); 7.48 (brs, 1H); 8.05 (s, 1H); 8.11 (s, 1H); 8.74 (s, 1H); 8.85 (s, 1H); 9.76 (s, 1H).
The title compound was synthesized by a method analogous to the synthesis of Example 137 starting with 1-ethyl-3-(5′-(hydrazinecarbonyl)-4-(5-methyl-4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridin-6-yl)urea Intermediate 237 and 1,1,1-trimethoxyethane.
MS (ESP): 490 (M+1) for C21H18F3N7O2S
1H-NMR (DMSO-d6) δ: 1.11 (t, 3H); 2.52 (s, 3H); 2.60 (s, 3H); 3.09-3.29 (m, 2H); 7.58 (br s, 1H); 8.18 (s, 1H); 8.31 (s, 1H); 8.36 (s, 1H); 8.70 (d, 1H); 9.17 (d, 1H); 9.51 (s, 1H).
The following compounds have been synthesized as described for Example 21 from the starting materials indicated in the table below.
The following compounds have been synthesized as described for Example 6 from the starting materials indicated in the table below.
To a solution 1-ethyl-3-(5′-(5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)-4-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridin-6-yl)urea (Example 6, 130 mg, 0.27 mmol) in ethanol (5 mL), N,N-dimethylpropane-1,3-diamine (41.7 mg, 0.41 mmol) was added and microwaved at 100° for 2 h. The reaction was concentrated and the crude resulted was taken in acetonitrile (5 mL), and 2,3,4,6,7,8,9,10-octahydropyrimido[1,2-a]azepine (0.081 mL, 0.54 mmol) (DBU) was added to it. Then triphenyl phosphine (143 mg, 0.54 mmol) followed by perchloromethane (0.053 mL, 0.54 mmol) (carbon tetrachloride) were added to the resulting solution and stirred over the weekend at room temperature. The solvent was removed and the crude was partitioned between water and ethyl acetate. The layers were separated. The aqueous layer was saturated with sodium chloride and extracted with ethyl acetate. The combined layers were washed with brine and dried over magnesium sulfate, concentrated and purified by normal phase (2% MeOH in DCM to 15% MeOH in DCM with 1% ammonium hydroxide). The fractions containing the products were combined and concentrated to give a white solid (34 mg).
MS (ESP): 562 (M+1) for C24H26F3N9O2S
1H-NMR (DMSO-d6) δ: 1.11 (t, 3H); 1.52-1.78 (m, 2H); 2.15 (s, 6H); 2.25-2.35 (m, 2H); 3.10-3.32 (m, 4H); 7.56 (brs, 1H); 7.93 (t, 1H); 8.09 (s, 1H); 8.24 (s, 1H); 8.39 (s, 1H); 8.57 (s, 1H); 8.61 (d, 1H); 9.01 (d, 1H); 9.51 (s, 1H)
The following compounds have been synthesized as described for Example 152 from the starting materials indicated in the table below.
To a solution of 1-ethyl-3-(5′-(5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)-4-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridin-6-yl)urea (example 6) (150 mg, 0.31 mmol) in THF (3 mL), potassium t-butoxide (0.377 mL, 0.38 mmol) was added at room temperature. It resulted a mixture that was stirred for 15 minutes and then dimethylcarbamic chloride (0.058 mL, 0.63 mmol) was added. Then the resulting mixture was stirred for one hour at room temperature and at 60° C. over night. The solvent was removed and the crude was diluted with water and extracted with ethyl acetate. The organic layer was washed with water several times followed by brine and dried over magesium sulfate, filtered then concentrated and purified by normal phase chromatography to isolate the desired product as a white solid (53 mg).
MS (ESP): 549 (M+1) for C22H19F3N8O4S
1H-NMR (DMSO-d6) δ: 1.11 (t, 3H); 3.05 (brs, 6H); 3.15-3.28 (m, 2H); 7.55 (brs, 1H); 8.22 (d, 1H); 8.24 (s, 1H); 8.39 (s, 1H); 8.60 (s, 1H); 8.71 (d, 1H); 9.04 (d, 1H); 9.52 (s, 1H)
The following compounds have been synthesized as described for Example 158 from the starting materials indicated in the table below.
To a suspension of 1-(5′-cyano-4-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridin-6-yl)-3-ethylurea (Example 2, 70 mg, 0.17 mmol) in ethanol (3 mL), hydroxylamine (0.015 mL, 0.25 mmol) (50% by weight, aq.) was added and microwaved at 80° C. for 1 h. The reaction was concentrated to give a white solid. It was slurried in acetonitrile, filtered and dried to give a white solid (52 mg).
MS (ESP): 452 (M+1) for C18H16F3N7O2S
1H-NMR (DMSO-d6) δ: 1.11 (t, 3H); 3.10-3.27 (m, 2H); 6.02 (s, 2H); 7.57 (brs, 1H); 8.03 (s, 1H); 8.26 (s, 1H); 8.35 (s, 1H); 8.46 (d, 1H); 8.56 (s, 1H); 8.93 (d, 1H); 9.48 (s, 1H); 9.91 (s, 1H)
To a solution of sodium methoxide (50 μl, 0.22 mmol) (25% by wt solution in MeOH) in MeOH (3 mL), 1-(5′-cyano-4-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridin-6-yl)-3-ethylurea (Example 2, 85 mg, 0.20 mmol) was added and the resulting mixture was stirred at room temperature for 4 hours. Then ammonium chloride (13.04 mg, 0.24 mmol) was added and the mixture was stirred overnight at room temperature. As there was no reaction the reaction mixture was transferred to a microwave vial and microwaved at 80° for 20 minutes.
The reaction was complete. The solid formed was filtered off and the washed with acetonitrile and dichloromethane. Then the solid was taken in water and sodium bicarbonate was added to it. The mixture was extracted with ethyl acetate. The extract was washed with water and dried over magnesium sulfate and concentrated to give a white solid which was slurried in acetonitrile, filtered and dried to give a white solid as the product (35 mg).
MS (ESP): 436 (M+1) for C18H16F3N7OS
1H-NMR (DMSO6) δ: 1.11 (t, 3H); 3.10-3.27 (m, 2H); 6.44 (brs, 2H); 6.55 (brs, 1H); 7.59 (brs, 1H); 8.17 (brs, 1H); 8.26 (s, 1H); 8.35 (s, 1H); 8.52 (s, 1H); 8.56 (s, 1H); 9.06 (brs, 1H); 9.48 (s, 1H)
To a solution of (S)-tert-butyl 1-(5-(6′-(3-ethylureido)-4′-(3-(trifluoromethyl)-1H-pyrazol-1-yl)-3,3′-bipyridin-5-yl)-1,3,4-oxadiazol-2-yl)-2-methylpropylcarbamate (Intermediate 257, 65 mg, 0.11 mmol), in dioxane (3 mL), 4M HCl in dioxane (3 mL, 86.39 mmol) was added and the mixture was allowed to stir overnight. The reaction was concentrated and the solid obtained was taken in water, basified with 1N NaOH to precipitate the product.
MS (ESP): 516 (M+1) for C23H24F3N9O2
1H-NMR (DMSO-d6) δ: 0.87 (d, 3H); 0.96 (d, 3H); 1.11 (t, 3H); 1.88-208 (m, 1H); 3.10-3.27 (m, 2H); 3.88 (d, 1H); 6.94 (d, 2H); 7.42 (brs, 1H); 7.93 (s, 1H); 7.94 (s, 1H); 7.97 (s, 1H); 8.14 (d, 1H); 8.50 (d, 1H); 8.57 (s, 1H); 9.12 (d, 1H); 9.62 (s, 1H).
To a suspension of 1-(5′-(2-(cyclopropanecarbonyl)hydrazinecarbonyl)-4-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridin-6-yl)-3-ethylurea (Intermediate 258, 80 mg, 0.15 mmol), triethylamine (0.021 mL, 0.15 mmol) and triphenylphosphine (81 mg, 0.31 mmol) were added followed by carbon tetrachloride (0.015 mL, 0.15 mmol). The resulting mixture was stirred at 40° C. for 1 h, then concentrated and the crude was partitioned between water and ethyl acetate. The layers separated and the organic layer was washed with water and brine, dried over magnesium sulfate and concentrated. The crude was purified by normal phase chromatography (1% MeOH in DCM to 5%). The fractions containing the product were combined, concentrated and lyophilized to give a white solid (42 mg).
MS (ESP): 502 (M+1) for C22H18F3N7O2S
1H-NMR (DMSO-d6) δ: 0.72-155 (m, 4H); 1.10 (t, 3H); 2.19-2.46 (m, 1H); 3.08-3.29 (m, 2H); 7.56 (brs, 1H); 8.23 (s, 1H); 8.28 (t, 1H); 8.40 (s, 1H); 8.57 (s, 1H); 8.68 (s, 1H); 9.15 (s, 1H); 9.52 (s, 1H).
The following Examples were synthesized from the general procedure described below from the starting materials in the Table.
A suspension of corresponding carboxylic acid (0.3 mmol), hydrazine acetate (0.9 mmol) in phosphorus oxychloride (2.5 mL) was heated at 70° C. for 2 h. The solution was then cooled and concentrated to dryness. A solution of saturated potassium carbonate was added to the crude and extracted with ethyl acetate (3×). The combined organic layers were washed with brine and dried over sodium sulfate. The solvent was removed under vacuum and the crude was purified by Analogix using dichloromethane-methanol.
A suspension of 6′-(3-propylureido)-2-(tetrahydro-2H-pyran-4-yloxy)-4′-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridine-5-carboxylic acid (Intermediate 262, ˜0.3 mmol) and hydrazine acetate (0.9 mmol) in phosphorus oxychloride (2.5 mL) was heated at 70° C. for 2 h. The solution was then cooled and concentrated to dryness. A solution of saturated potassium carbonate was added to the crude and extracted with ethyl acetate (3×). The combined organic layers were washed with brine and dried over sodium sulfate. The solvent was removed under vacuum and the crude was purified by Analogix using dichloromethane-methanol.
MS (ESP): 590.1 (MH+) for C26H26F3N7O4S
1H NMR (300 MHz, CDCl3): δ 1.002-1.05 (m, 3H), 1.25-1.28 (m, 2H), 1.65-1.75 (m, 4H), 2.62 (s, 3H), 3.39-3.47 (m, 4H), 3.64-3.68 (m, 2H), 5.10-5.18 (m, 1H), 7.61 (s, 1H), 7.73 (s, 1H), 8.20 (s, 1H), 8.24-8.26 (m, 1H), 8.83 (m, 1H), 9.12 (bs, 1H), 9.48 (bs, 1H)
19F NMR (300 MHz, CDCl3): δ −64.51
The following Examples were prepared by the general procedure described below from the starting materials indicated in the Table.
A suspension of corresponding carboxylic acid (0.3 mmol) in thionyl chloride (2 mL) was heated at 50° C. for 1 h. The solution was then cooled and concentrated to dryness. The crude suspended in tetrahydrofuran (2 mL) was added slowly to a solution of hydrazine/tetrahydrofuran (1/2 vol., 3 mL) and stirred at room temperature for 12 h. After this period of time, the crude was concentrated to dryness and purified by reverse phase on Analogix C18-column (water-methanol) to give (˜60%) hydrazides as off-white solids. A suspension of corresponding hydrazide (0.3 mmol) in anhydrous tetrahydrofuran (2 mL) was treated with triethyl amine (0.6 mmol) and 1,1′-carbonyl diimidazole (0.12 mmol). The reaction was stirred at room temperature for 12 h, concentrated to dryness and purified directly by Analogix using dichloromethane-methanol to give (˜50%) product as an off-white solid.
Methyl 6′-(3-propylureido)-4′-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridine-5-carboxylate (Intermediate 263, 140 mg) was dissolved in tetrahydrofuran (3 mL) and methanol (3 mL).
1N Sodium hydroxide (3 mL) was added, and the reaction was stirred at room temperature for 3 h. The organics were removed and the residual aqueous phase was acidified to pH ˜2 with 1N hydrochloric acid. The mixture was filtered and the solid dried in a vacuum oven at 50° C. for 18 h. The solid was then dissolved in phosphorous oxychloride (3 mL), acetic hydrazide (25 mg) was added and the solution heated at 60° C. for 3 h. Most of the phosphorous oxychloride was removed in vacuo and then saturated sodium bicarbonate was added to the mixture to obtain a pH ˜7. The solution was extracted with 2:1 ethyl acetate: tetrahydrofuran (3×, 3 mL each). The organic phases were combined, dried over sodium sulfate, and the solvent was removed in vacuo.
MS (ESP): 490.2 (M+H+) for C21H18F3N7O2S
1H NMR (300 MHz, DMSO-d6): δ 0.91 (t, 3H), 1.46-1.54 (m, 2H), 2.60 (s, 3H), 3.12-3.18 (m, 2H), 7.64 (bt, 1H), 8.24 (s, 1H), 8.30 (dd, 1H), 8.41 (d, 1H), 8.58 (d, 1H), 8.70 (d, 1H), 9.17 (d, 1H), 9.54 (bs, 1H)
Diethyl 2-(6-(3-propylureido)-4-(4-(trifluoromethyl)thiazol-2-yl)pyridin-3-yl)thiazole-4,5-dicarboxylate (Intermediate 264, 73 mg, 0.13 mmol), was dissolved in methanol (10 mL) and hydrazine (0.4 mL) was added. The reaction was heated at reflux for 3 h. 12 M Hydrochloric acid (1 mL) was then added and the reaction heated for a further 2 h. The solvents were removed in vacuo. The residue was chromatographed on the preparative HPLC to give 18 mg (26% yield) of 1-(5-(4,7-dihydroxythiazolo[5,4-d]pyridazin-2-yl)-4-(4-(trifluoromethyl)thiazol-2-yl)pyridin-2-yl)-3-propylurea as a tan solid.
MS (ESP): 498.0 (M+H+) for C18H14F3N7O3S2
1H NMR (300 MHz, DMSO-d6): δ 0.93 (t, 3H), 1.46-1.53 (m, 2H), 2.60 (s, 3H), 3.11-3.15 (m, 2H), 7.52 (bt, 1H), 8.17 (s, 1H), 8.71 (d, 1H), 8.78 (s, 1H), 9.76 (bs, 1H).
Methyl 6-(3-propylureido)-4-(4-(trifluoromethyl)thiazol-2-yl)-3,4′-bipyridine-2′-carboxylate (Intermediate 265, 65 mg, 0.14 mmol) was dissolved in ethanol (10 mL) and hydrazine monohydrate (1 mL) was added. The reaction was heated at reflux for 6 h. The solvent was removed in vacuo, and the residue was placed in a vacuum oven at 60° C. for 1 h. The residue was then dissolved in anhydrous tetrahydrofuran (10 mL). 1,1′-Carbonyl diimidazole (100 mg) was added and the reaction was stirred at 25° C. for 18 h. The solvent was removed in vacuo and the residue was subjected to preparative HPLC. This gave 19 mg (27% yield) of 1-(2′-(5-hydroxy-1,3,4-oxadiazol-2-yl)-4-(4-(trifluoromethyl)thiazol-2-yl)-3,4′-bipyridin-6-yl)-3-propylurea as a white powder.
MS (ESP): 492.0 (M+H+) for C20H17F3N6O3S
1H NMR (300 MHz, CD3OD): δ 0.99 (t, 3H), 1.61-1.63 (m, 2H), 3.11-3.15 (m, 2H), 7.44 (dd, 1H), 7.80 (s, 1H), 7.84 (dd, 1H), 8.28 (d, 1H), 8.39 (d, 1H) 8.62 (dd, 1H)
The following Examples were synthesized according to the procedure for Example 158 from the starting materials indicated in the Table.
The following Examples were synthesized according to the procedure for Example 166 from the starting materials indicated in the Table.
The following Examples were synthesized according to the procedure for Example 165 from the starting materials indicated in the Table.
The following Example was prepared according to the procedure described for Intermediate 2 using the starting materials indicated in the table.
The following Examples were prepared according to the procedure described for Example 33 using the starting materials indicated in the table.
The following Examples were prepared as described for Example 1 using the starting materials as indicated in the table.
In a 25 mL pear flask, 1-ethyl-3-(5′-(hydrazinecarbonyl)-4-(4-(1-methyl-1H-pyrazol-4-yl)thiazol-2-yl)-2′-(tetrahydro-2H-pyran-4-yloxy)-3,3′-bipyridin-6-yl)urea (Intermediate 366, 68.1 mg, 0.12 mmol) and 1,1,1-trimethoxyethane (461 μl, 3.62 mmol) were suspended in solvent. The reaction slurry was heated to reflux for 30 min. 2,3,4,6,7,8,9,10-octahydropyrimido[1,2-a]azepine (18.07 μl, 0.12 mmol) was added in a single portion. The reaction was heated for an additional for 2 h. The reaction mixture was cooled to room temperature, diluted with EtOAc and washed with water then brine. The organic phase was dried over Na2SO4, filtered and concentrated by rotary evaporation. The crude was purified by silica gel flash column chromatography (95:5 CH2Cl2/MeOH). Isolation gave 40 mg of the desired product.
LC/MS (ES+)[(M+H)+]: 588 for C28H29N9O4S.
1H NMR (300 MHz, d6-DMSO): 1.12 (t, 3H), 1.16 (m, 2H), 1.60 (m, 2H), 2.59 (s, 3H), 3.22 (m, 2H), 3.25 (m, 2H), 3.37 (m, 2H), 3.83 (s, 3H), 5.08 (m, 1H), 7.50 (s, 1H), 7.67 (m, 1H), 7.72 (s, 1H), 7.88 (s, 1H), 8.21 (s, 1H), 8.26 (s, 1H), 8.27 (m, 1H), 8.81 (m, 1H), 9.45 (s, 1H).
The following Examples were prepared according to the procedure as described by Example 231 using the starting materials as indicated.
In a glass vial, (S)-1-ethyl-3-(5′-(2-(2-(triethylsilyloxy)propanoyl)hydrazinecarbonyl)-4-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridin-6-yl)urea (Intermediate 403, 200 mg, 0.31 mmol) was suspended in a acetonitrile solution containing carbon tetrachloride (0.091 mL, 0.94 mmol) and diisopropylethyl amine (0.168 mL, 0.94 mmol). Triphenylphosphine (247 mg, 0.94 mmol) was added in a single portion. The reaction mixture was gently warmed to form a homogenous solution and was then allowed to stir at room temperature overnight. Once cyclized, the reaction mixture was acidified to pH=1 with 6N HCl. The reaction mixture was diluted with EtOAc, washed with NaHCO3 (sat.) then brine. Dried the organic phase over Na2SO4, filtered and concentrated to dryness by rotary evaporation. Purified by silica gel flash column chromatography (95:5 CH2Cl2/MeOH). Isolated 72 mg of the title compound.
LC/MS (ES+)[(M+H)+]: 506 for C21H18F3N7O3S.
1H NMR (300 MHz, d6-DMSO): 1.12 (t, 3H), 1.53 (d, 3H), 3.22 (m, 2H), 5.02 (m, 1H), 6.03 (d, 1H), 7.55 (t, 1H), 8.25 (s, 1H), 8.33 (t, 1H), 8.42 (s, 1H), 8.57 (s, 1H), 8.72 (d, 1H), 9.20 (d, 1H), 9.50 (s, 1H).
(S)-tert-butyl cyclohexyl(5-(6′-(3-ethylureido)-4′-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridin-5-yl)-1,3,4-oxadiazol-2-yl)methylcarbamate (Intermediate 404, 100 mg, 0.15 mmol) was dissolved in 1,4 dioxane. 4N HCl in dioxane (4 mL, 16.00 mmol) was added in a single portion. The solution was stirred at room temperature for 12 h. Concentrate the reaction mixture to dryness by rotary evaporation. Dissolve the crude in EtOAc, washed with 10% NaHCO3, dried over Na2SO4, filtered, concentrated and purified by silica gel flash column chromatography (95:5 CH2Cl2/MeOH). Isolation gave 63 mg of the title compound.
LC/MS (ES+)[(M+H)+]: 573 for C26H27F3N8O2S.
1H NMR (300 MHz, d6-DMSO): 1.01-1.21 (m, 5H), 1.12 (t, 3H), 1.44 (m, 1H), 1.69 (m, 4H), 1.85 (m, 1H), 2.16 (s, 2H), 3.22 (m, 2H), 3.88 (d, 1H), 7.55 (t, 1H), 8.24 (s, 1H), 8.30 (t, 1H), 8.42 (s, 1H), 8.57 (s, 1H), 8.72 (d, 1H), 9.20 (d, 1H), 9.51 (s, 1H).
The following Examples were prepared according to the procedures described for Example 238 using the starting materials indicated in the table.
1-ethyl-3-(5-(3-(2-hydroxyethyl)-1,4-dioxo-1,2,3,4-tetrahydrophthalazin-6-yl)-4-(4-trifluoromethyl)thiazol-2-pyridin-2-yl)urea and 1-ethyl-3-(5-(2-(2-hydroxyethyl-1,4-dioxo-1,2,3,4-tetrahydrophthalazin-6-yl)-4-(4-(trifluoromethyl)thiazol-2-yl)pyridin-2-yl)urea
6-(3-ethylureido)-4-(4-(trifluoromethyl)thiazol-2-yl)pyridin-3-ylboronic acid (Intermediate 12, 400 mg, 1.11 mmol), a 1:1 mixture of 6-bromo-2-(2-hydroxyethyl)-2,3-dihydrophthalazine-1,4-dione and 7-bromo-2-(2-hydroxyethyl)-2,3-dihydrophthalazine-1,4-dione (Intermediates 411 and 412, 348 mg, 1.22 mmol), Pd(PPh3)4 (64.2 mg, 0.06 mmol) and cesium carbonate (543 mg, 1.67 mmol) were combined in a microwave vessel and suspended in a 4:1 mixture of dioxane and water. The reaction slurry was degassed and purged with nitrogen. The reaction mixture was heated in the microwave at 100° C. for 2 hours. The reaction mixture was concentrated to dryness by rotary evaporation. The residue was dissolved in minimal DMSO and water to help solubilize the inorganic salts. The two regioisomers were separated by reverse phase (C30 column) Gilson HPLC (10-50% MeOH/0.1% formic acid).
Isolated 38 mg. LC/MS (ES+)[(M+H)+]: 521 for C22H19F3N6O4S. 1H NMR (300 MHz, d6-DMSO): 1.04 (t, 3H), 3.14 (m, 2H), 3.66 (t, 2H), 3.98 (t, 2H), 7.57 (t, 1H), 7.65 (d, 1H), 7.83 (s, 1H), 8.12 (d, 1H), 8.17 (s, 1H), 8.27 (s, 1H), 8.41 (s, 1H), 9.48 (s, 1H).
Isolated 37 mg. LC/MS (ES+)[(M+H)+]: 521 for C22H19F3N6O4S. 1H NMR (300 MHz, d6-DMSO): 1.04 (t, 3H), 3.14 (m, 2H), 3.66 (t, 2H), 3.97 (t, 2H), 7.56 (t, 1H), 7.69 (dd, 1H), 7.92 (d, 1H), 8.06 (d, 1H), 8.17 (s, 1H), 8.28 (s, 1H), 8.42 (s, 1H), 9.45 (s, 1H).
To a mixture of 6-(3-ethylureido)-4-(4-(6-methoxypyridin-2-yl)thiazol-2-yl)pyridin-3-ylboronic acid (Intermediate 415, 270 mg, 0.68 mmol), 5-bromopyridine-3-sulfonamide (192 mg, 0.81 mmol), Pd2 dba3 (31.0 mg, 0.03 mmol), dicyclohexyl(2′,4′,6′-triisopropylbiphenyl-2-yl)phosphine (97 mg, 0.20 mmol), and cesium carbonate (264 mg, 0.81 mmol) under vacuum, was added 1,4-dioxane (20 mL), water (5 mL), the reaction was then heated to 80° C. in an oil bath, purged with nitrogen, then stirred at that temperature under nitrogen pressure for 45 minutes. The reaction was then diluted with ethyl acetate (100 ml) and water (100 ml), then the layers were separated. The aqueous phase was extracted with ethyl acetate (3×100 ml), then the organics were combined, washed with brine, dried over sodium sulfate, filtered, concentrated under reduced pressure. The residue was suspended in methylene chloride with 5% methanol, loaded onto a silica gel column, eluted with a gradient of methanol in methylene chloride to give the desired product as a tan gum, which was suspended in dichloromethane and filtered to give the title compound as a pale tan solid (30 mg, 8.6%).
MS (EI) (M+H)+ 512 for C22H22N7O4S2 (M−H)− 510 for C22H20N7O4S2
1H NMR (DMSO-d6) δ: 9.51 (s, 1H), 8.98 (d, J=2.07 Hz, 1H), 8.73 (d, J=1.88 Hz, 1H), 8.34 (s, 1H), 8.32 (s, 1H), 8.29 (s, 1H), 8.18 (s, 1H), 7.73 (t, J=7.82 Hz, 1H), 7.66 (s, 1H), 7.58 (t, J=4.71 Hz, 1H), 7.22 (d, J=7.35 Hz, 1H), 6.78 (d, J=8.29 Hz, 1H), 3.92 (s, 3H), 3.22 (dq, J=6.88, 6.56 Hz, 2H), 1.11 (t, J=7.16 Hz, 3H)
A solution of 1-ethyl-3-(2′-(hydrazinecarbonyl)-4-(4-(6-methoxypyridin-2-yl)thiazol-2-yl)-3,4′-bipyridin-6-yl)urea (Intermediate 416, 91 mg, 0.19 mmol) in DMF (2 mL) was treated with di(1H-imidazol-1-yl)methanone (60 mg, 0.37 mmol), warmed to 50° C. in an oil bath for 20 min, and cooled to room temperature. The reaction was held at room temperature for 1 hour, diluted with ethyl acetate (50 ml), washed with water (2×50 ml) and brine (30 ml). The organic layer was dried over magnesium sulfate, filtered and concentrated under reduced pressure to afford a tan mass. This material was suspended into acetonitrile (20 ml), warmed to reflux and cooled to give the title compound as a tan powder (70 mg, 73.1%).
MS (EI) (M+H)+ 517 for C24H21N8O4S (M−H)− 515 for C24H19N8O4S
1H NMR (DMSO-d6) δ: 12.77 (br. s., 1H), 9.52 (s, 1H), 8.70 (d, J=4.90 Hz, 1H), 8.35 (s, 1H), 8.35 (s, 1H), 8.22 (s, 1H), 7.90 (s, 1H), 7.70 (t, J=7.82 Hz, 1H), 7.58 (br. s., 1H), 7.54 (d, J=5.09 Hz, 1H), 7.20 (d, J=7.35 Hz, 1H), 6.78 (d, J=8.29 Hz, 1H), 3.91 (s, 3H), 3.22 (quin, J=6.69 Hz, 2H), 1.11 (t, J=7.16 Hz, 3H);
A suspension of 1-ethyl-3-(2′-(hydrazinecarbonyl)-4-(4-(6-methoxypyridin-2-yl)thiazol-2-yl)-3,4′-bipyridin-6-yl)urea (Intermediate 416, 80 mg, 0.16 mmol) in 1,1,1-trimethoxyethane (5 mL, 41.62 mmol) was treated with concentrated aqueous HCl (drop), and the resulting solution was heated to reflux for 5 minutes, the resulting pink solution was treated with DBU (0.1 mL, 0.66 mmol) and refluxed for an additional 30 minutes at which point solvent was removed and the residue purified by flash chromatography eluting with a gradient of methanol in methylene chloride to give the desired product as a tan solid (9 mg, 10.72%).
MS (EI) (M+H)+ 515 for C25H23N8O3S) (M−H)− 513 for C25H21N8O3S
1H NMR (DMSO-d6) δ: 9.48-9.64 (m, 1H), 8.75 (d, J=5.09 Hz, 1H), 8.38 (s, 1H), 8.35 (s, 1H), 8.23 (s, 1H), 8.11 (s, 1H), 7.66 (t, J=7.82 Hz, 1H), 7.54-7.63 (m, 2H), 7.18 (d, J=7.35 Hz, 1H), 6.76 (d, J=8.29 Hz, 1H), 3.90 (s, 3H), 3.12-3.25 (m, 2H), 2.59 (s, 3H), 1.11 (t, J=7.16 Hz, 3H);
To a mixture of 6-(3-ethylureido)-4-(4-(6-methoxypyridin-2-yl)thiazol-2-yl)pyridin-3-ylboronic acid (Intermediate 415, 510 mg, 0.15 mmol), 2-(5-bromopyridin-3-yl)-5-methyl-1,3,4-oxadiazole (Intermediate 418, 36.8 mg, 0.15 mmol), dicyclohexyl(2′,4′,6′-triisopropylbiphenyl-2-yl)phosphine (21.92 mg, 0.05 mmol), Pd2dba3 (7.02 mg, 7.66 μmol), and Cs2CO3 (59.9 mg, 0.18 mmol), under vacuum was added 1,4-dioxane (20 mL), water (5 mL), and the resulting suspension was heated in an oil bath at 80° C., placed under nitrogen, and held at that temperature for 1 hour. The reaction mixture was cooled to room temperature, diluted with ethyl acetate (100 ml) and washed with water. The aqueous phase was extracted with ethyl acetate (2×50 ml), and the combined organics were washed with brine, dried over magnesium sulfate, filtered, and concentrated under reduced pressure. The residue was purified by flash chromatography on silica gel eluting with a gradient of ethyl acetate in hexanes to give the title compound as a cream colored solid (20 mg, 25.4%).
MS (EI) (M+H)+ 515 for C25H23N8O3S (M−H)− 513 for C25H21N8O3S
1H NMR (DMSO-d6) δ: 9.50 (s, 1H), 9.16 (d, J=2.07 Hz, 1H), 8.75 (d, J=1.88 Hz, 1H), 8.37 (s, 1H), 8.36 (t, J=2.07 Hz, 1H), 8.33 (s, 1H), 8.28 (s, 1H), 7.69 (t, J=7.82 Hz, 1H), 7.60 (t, J=5.75 Hz, 1H), 7.23 (d, J=7.35 Hz, 1H), 6.77 (d, J=8.10 Hz, 1H), 3.90 (s, 3H), 3.17-3.28 (m, 2H), 2.57 (s, 3H), 1.12 (t, J=7.16 Hz, 3H);
A mixture of 1-ethyl-3-(5-(5-(hydrazinecarbonyl)-4-(1-methyl-1H-1,2,4-triazol-5-yl)thiazol-2-yl)-4-(4-(6-methoxypyridin-2-yl)thiazol-2-yl)pyridin-2-yl)urea (Intermediate 419, 115 mg, 0.20 mmol) and 1,1′-carbonyl diimidazole (120 mg, 0.74 mmol) was suspended in DMF (3 mL) and heated to 110° C. for 20 min. The grey suspension was filtered hot, the filtrate was then treated with water (9 ml) and allowed to cool slowly, the resulting yellow precipitate was collected by filtration, washed with methanol to give the title compound as a pale yellow solid (30 mg, 24.96%).
MS (EI) (M+H)+ 604 for C25H22N11O4S2 (M−H)− 602 for C25H20N11O4S2
1H NMR (DMSO-d6) δ: 12.58-12.96 (m, 1H), 9.71 (s, 1H), 8.82 (s, 1H), 8.49 (s, 1H), 8.17 (s, 1H), 8.07 (s, 1H), 7.73 (t, J=7.82 Hz, 1H), 7.51 (t, J=5.84 Hz, 1H), 7.41 (d, J=7.35 Hz, 1H), 6.81 (d, J=8.10 Hz, 1H), 3.95 (s, 3H), 3.79 (s, 3H), 3.13-3.28 (m, 2H), 1.11 (t, J=7.16 Hz, 3H);
A suspension of 1-ethyl-3-(5-(5-(hydrazinecarbonyl)-4-(1-methyl-1H-1,2,4-triazol-5-yl)thiazol-2-yl)-4-(4-(6-methoxypyridin-2-yl)thiazol-2-yl)pyridin-2-yl)urea (Intermediate 419, 50 mg, 0.08 mmol) in DMF (2 ml) and 1,1,1-trimethoxyethane (5 ml, 41.62 mmol) was treated with aqueous HCl (1 drop), heated to 100° C. for 15 minutes, then treated with DBU (1 ml) and refluxed for 5 minutes. The reaction mixture was then cooled, diluted with water (25 ml) and ethyl acetate (100 ml), and the layers were separated. The organic phase was washed sequentially with saturated sodium hydrogen carbonate, brine, then dried over magnesium sulfate. The solvent was removed under reduced pressure and the residue was purified by chromatography on silica gel eluting with a gradient of methanol in methylene chloride. The appropriate fractions were pooled and the crude product was precipitated from ethyl acetate with hexanes to give product as a pale yellow solid (15 mg, 15%).
MS (EI) (M+H)+ 602 for C26H24N11O3S2 (M−H)− 600 for C26H22N11O3S2
1H NMR (DMSO-d6) δ: 9.72 (s, 1H), 8.85 (s, 1H), 8.49 (s, 1H), 8.17 (s, 1H), 8.04 (s, 1H), 7.71 (t, J=7.82 Hz, 1H), 7.51 (t, J=4.99 Hz, 1H), 7.41 (d, J=7.35 Hz, 1H), 6.80 (d, J=8.29 Hz, 1H), 3.94 (s, 3H), 3.81 (s, 3H), 3.10-3.28 (m, 2H), 2.50 (br. s., 3H), 1.11 (t, J=7.06 Hz, 3H);
To a mixture of 1-ethyl-3-(5′-(hydrazinecarbonyl)-4-(4-(pyridin-4-ylmethyl)thiazol-2-yl)-3,3′-bipyridin-6-yl)urea (Intermediate 421, 55 mg, 0.12 mmol) in THF (10 ml) was added di(1H-imidazol-1-yl)methanone (75 mg, 0.46 mmol) and the resulting suspension was warmed slightly to afford a solution which was stirred at room temperatere for one hour at which point the solvents were removed under reduced pressure and the resulting solid was dissolved in ethyl acetate (50 ml), methanol (5 ml), and water (50 ml). The layers were separated, and the organic phase was washed sequentially with saturated aqueous sodium hydrogen carbonate and brine, dried over magnesium sulfate, filtered, concentrated, and purified by normal phase chromatography eluting on silica gel with a gradient of methanol in dichloromethane to afford 40 mg (61%) of the title compound as an off white powder.
MS (EI) (M+H)+ 501 for C24H21N8O3S (M−H)− 499 for C24H19N8O3S;
1H NMR (DMSO-d6) δ: 12.59 (br. s., 1H), 9.47 (s, 1H), 8.89 (d, J=1.70 Hz, 1H), 8.59 (d, J=1.70 Hz, 1H), 8.36 (d, J=5.65 Hz, 2H), 8.29 (s, 1H), 8.06 (s, 1H), 7.93 (s, 1H), 7.67 (br. s., 1H), 7.58 (s, 1H), 7.03 (d, J=5.27 Hz, 2H), 3.99 (s, 2H), 3.20 (dq, J=6.97, 6.59 Hz, 2H), 1.10 (t, J=7.06 Hz, 3H);
To a solution of ethyl 6′-(3-ethylureido)-6-(2-methoxyethoxy)-4′-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridine-5-carboxylate (Intermediate 425, 90 mg, 0.05 mmol) in ethanol (10 mL) was added hydrazine (200 μL, 6.24 mmol). The solution was heated to reflux for 1 hour, solvents were removed, and the resulting gum was taken up into THF (10 ml) and treated with 1,1′-carbonyl di-imidazole (2×50 mg). The resulting solution was stirred at RT for 8 hours. The solvents were removed and the residue was purified by normal phase chromatography eluting with a gradient of methanol in dichloromethane, to afford crude product, which was purified by normal phase chromatography eluting with a gradient of ethyl acetate in hexanes to give the title compound as an off white solid.
MS (EI) (M+H)+ 551 for C22H21F3N7O5S (M−H)− 549 for C22H19F3N7O5S;
1H NMR (DMSO-d6) δ: 12.65 (s, 1H), 9.44 (s, 1H), 8.49 (s, 1H), 8.28 (s, 1H), 8.23 (d, J=1.70 Hz, 2H), 7.67 (t, J=4.71 Hz, 1H), 7.15 (s, 1H), 4.49 (dd, J=5.37, 3.11 Hz, 2H), 3.71 (t, J=4.33 Hz, 2H), 3.31 (br. s., 3H), 3.14-3.27 (m, 2H), 1.11 (t, J=7.25 Hz, 3H);
19F-NMR (DMSO-d6) δ −62.51 (br. s., 3 F);
A mixture of 6-(3-ethylureido)-4-(4-(trifluoromethyl)thiazol-2-yl)pyridin-3-ylboronic acid (Intermediate 12, 300 mg, 0.83 mmol), potassium carbonate (142 mg, 1.03 mmol), palladium diphenylphosphinoferocene dichloride (50.0 mg, 0.07 mmol) and 3-bromo-5-(5-methyl-1,3,4-oxadiazol-2-yl)pyridine 1-oxide (Intermediate 428, 175 mg, 0.68 mmol) was treated with acetonitrile (10 mL) under vacuum. Water (10.00 mL) was added and after degassing for 1 minute the suspension was heated to 80° C. for 30 minutes. The reaction was then cooled to RT, diluted with ethyl acetate (100 ml) and methanol (10 ml). The organic layer were washed with water, saturated bicarbonate, and brine, and the aqueous phase was back extracted with ethyl acetate (2×100 ml). The combined organics were washed with brine, dried over magnesium sulfate, filtered, and the solvent removed under reduced pressure. The residue was purified by normal phase chromatography on silica gel eluting with a gradient of methanol in dichloromethane. The major peak was concentrated down to a pale amber solid which was suspended in dichloromethane and filtered to give 170 mg of the title compound as a white solid.
MS (EI) (M+H)+ 492 for C20H17F3N7O3S (M−H) 490 for C20H15F3N7O3S;
1H NMR (DMSO-d6) δ: 9.54 (s, 1H), 8.71 (s, 1H), 8.63 (s, 1H), 8.53 (s, 1H), 8.40 (s, 1H), 8.23 (s, 1H), 7.77 (s, 1H), 7.52 (t, J=4.99 Hz, 1H), 3.14-3.28 (m, J=7.16, 7.16, 6.22, 6.22 Hz, 2H), 2.58 (s, 3H), 1.10 (t, J=7.16 Hz, 3H);
19F-NMR (DMSO-d6) δ: −62.57 (s, 3 F);
A mixture of 3-bromo-5-(5-(difluoromethyl)-4H-1,2,4-triazol-3-yl)pyridine (Intermediate 429, 76 mg, 0.28 mmol), 6-(3-ethylureido)-4-(4-(trifluoromethyl)thiazol-2-yl)pyridin-3-ylboronic acid (Intermediate 12, 100 mg, 0.28 mmol), cesium carbonate (181 mg, 0.56 mmol), DicyclohexylTriisopropylBiphenylphosphine (39.7 mg, 0.08 mmol), and dipalladium(0)trisdibenzilidineacetone (12.71 mg, 0.01 mmol) in 1,4-dioxane (12 mL) was degassed, treated with water (3 mL) and heated to 80° C. for 30 minutes. The reaction was diluted with ethyl acetate (100 ml) and water (100 ml) and the layers were separated. The aqueous phase was extracted with ethyl acetate (3×50 ml), and the combined organics were washed with brine, dried over magnesium sulfate, and filtered. The solvent was removed under reduced pressure, and the residue was purified by normal phase chromatography on silica gel, first eluting with a gradient of ethyl acetate in hexanes to provide crude product which was further purified by normal phase chromatography on silica gel eluting with a gradient of methanol in dichloromethane to afford a tan solid which was triturated from dichloromethane with hexanes to afford 50 mg of the title compound as a beige solid.
MS (EI) (M+H)+ 511 for C20H16F5N8OS (M−H)− 509 for C20H14F5N8OS;
1H NMR (DMSO-d6) δ: 15.19 (br. s., 1H), 9.52 (s, 1H), 9.22 (d, J=0.94 Hz, 1H), 8.64 (s, 1H), 8.55 (s, 1H), 8.40 (s, 1H), 8.34 (br. s., 1H), 8.27 (s, 1H), 7.55 (t, J=5.09 Hz, 1H), 7.19 (t, J=53.50 Hz, 1H), 3.21 (quin, J=6.73 Hz, 2H), 1.11 (t, J=7.06 Hz, 3H);
19F-NMR (DMSO-d6) δ: −62.49 (s, 3 F), −116.16 (br. s., 2 F);
Example 257 was synthesized as described for Example 256 from Intermediate 431 and Intermediate 12 as a tan solid.
MS (EI) (M+H)+ 529 for C20H15F6N8OS (M−H)− 527 for C20H13F6N8OS
1H NMR (DMSO-d6) δ: 15.56 (br. s., 1H), 9.52 (s, 1H), 9.22 (s, 1H), 8.66 (s, 1H), 8.52-8.61 (m, 1H), 8.41 (s, 1H), 8.36 (s, 1H), 8.26 (s, 1H), 7.54 (t, J=5.09 Hz, 1H), 3.21 (dq, J=6.97, 6.66 Hz, 2H), 1.11 (t, J=7.16 Hz, 3H);
19F-NMR (DMSO-d6) δ: −62.52 (s, 3 F), −63.75 (br. s., 3 F);
Example 258 was synthesized according to the procedure for Example 255 from Intermediate 12 and Intermediate 434 as an off white solid.
MS (EI) (M+H)+ 491 for C20H18F3N8O2S (M−H)− 489 for C20H16F3N8O2S;
1H NMR (DMSO-d6) δ: 9.41 (s, 1H), 8.52 (s, 1H), 8.30 (s, 1H), 8.25 (s, 1H), 8.13 (d, J=2.26 Hz, 1H), 7.96 (d, J=2.45 Hz, 1H), 7.63 (t, J=4.52 Hz, 1H), 7.53 (br. s., 2H), 3.20 (quin, J=6.59 Hz, 2H), 2.54 (s, 3H), 1.10 (t, J=7.16 Hz, 3H);
19F-NMR (DMSO-d6) δ: −62.33 (s, 3 F);
Example 259 was synthesized according to the procedure for Example 255 from Intermediate 12 and Intermediate 436 as a white solid.
MS (EI) (M+H)+ 492 for C20H17F3N7O3S (M−H) 490 for C20H15F3N7O3S;
1H NMR (DMSO-d6) δ: 9.53 (s, 1H), 8.64 (s, 1H), 8.47 (d, J=6.97 Hz, 1H), 8.40 (s, 1H), 8.18 (s, 1H), 7.91 (d, J=2.45 Hz, 1H), 7.56 (dd, J=6.78, 2.26 Hz, 1H), 7.49 (t, J=4.71 Hz, 1H), 3.11-3.25 (m, 2H), 2.61 (s, 3H), 1.10 (t, J=7.16 Hz, 3H);
19F-NMR (DMSO-d6) δ: −62.47 (s, 3 F);
Example 260 was synthesized according to the procedure for Example 255 from Intermediate 12 and Intermediate 437 as a pale yellow solid.
MS (EI) (M+H)+ 493 for C19H16F3N8O3S (M−H)− 491 for C19H14F3N8O3S;
1H NMR (DMSO-d6) δ: 12.40 (br. s., 1H), 9.43 (s, 1H), 8.50 (s, 1H), 8.48 (d, J=2.26 Hz, 1H), 8.34 (s, 1H), 8.17 (s, 1H), 7.82 (t, J=5.56 Hz, 1H), 7.69 (d, J=2.26 Hz, 1H), 6.51 (br. s., 2H), 3.15-3.27 (m, 2H), 1.10 (t, J=7.16 Hz, 3H)
19F-NMR (DMSO-d6) δ: −62.29 (s, 3 F)
Perchloromethane (19.32 mg, 0.13 mmol) was added to a solution of crude 1454542-acetylhydrazinecarbonyl)-6-oxo-1,6-dihydropyridin-3-yl)-4-(4-(trifluoromethyl)thiazol-2-yl)pyridin-2-yl)-3-ethylurea (Intermediate 441, 16 mg, 0.03 mmol), triphenylphosphine (16.47 mg, 0.06 mmol), and DBU (9.47 μL, 0.06 mmol) in acetonitrile (5 mL) and the mixture was stirred for 80 hours at RT. The reaction was purified by normal phase chromatography on silica gel eluting with a gradient of methanol in dichloromethane to afford 10 mg of the title compound as an off white solid.
MS (EI) (M+H)+ 492 for C20H17F3N7O3S (M−H)− 490 for C20H15F3N7O3S;
1H NMR (DMSO-d6) δ: 12.64 (br. s., 1H), 9.42 (s, 1H), 8.60 (s, 1H), 8.32 (s, 1H), 8.24 (s, 1H), 7.97 (d, J=2.64 Hz, 1H), 7.82 (s, 1H), 7.59 (t, J=5.09 Hz, 1H), 3.20 (dq, J=6.97, 6.59 Hz, 2H), 2.52 (br. s., 3H), 1.10 (t, J=7.16 Hz, 3H)
19F-NMR (DMSO-d6) δ: −62.39 (s, 3 F)
1,1′-Carbonyl di-imidazole (CDI, 50 mg, 0.31 mmol) was added to a solution of crude 1-ethyl-3-(5-(6-(hydrazinecarbonyl)pyrazin-2-yl)-4-(4-(6-methoxypyridin-2-yl)thiazol-2-yl)pyridin-2-yl)urea (Intermediate 446, 30 mg, 0.06 mmol) in tetrahydrofuran (10 mL) and DIEA (100 μL, 0.57 mmol). The amber solution was treated with CDI (3×20 mg), solvent was removed under reduced pressure, purified by normal phase chromatography on silica gel eluting with a gradient of methanol in dichloromethane, the crude product was dissolved in ethyl acetate (50 ml), washed with water (50 ml). The aqueous layer was back extracted with ethyl acetate (2×50 ml), combined organics were washed with brine, dried over magnesium sulfate, filtered, and concentrated to give 23 mg of the title compound as a pale off white solid.
MS (EI) (M+H)+ 518 for C23H20N9O4S (M−H)− 516 for C23H18N9O4S;
1H NMR (DMSO-d6) δ: 9.64 (s, 1H), 9.06 (s, 1H), 8.77 (s, 1H), 8.49 (s, 1H), 8.36 (s, 1H), 8.28 (s, 1H), 7.71 (d, J=7.91 Hz, 1H), 7.59-7.67 (m, 1H), 6.86-7.10 (m, 2H), 6.76 (d, J=8.29 Hz, 1H), 3.91 (s, 3H), 3.22 (quin, J=6.69 Hz, 2H), 1.12 (t, J=7.25 Hz, 3H)
Potassium carbonate (1 ml, 1N in water) was added to a solution of 2-(5-(6′-(3-ethylureido)-4′-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridin-5-yl)-1,3,4-oxadiazol-2-yl)propan-2-yl acetate (Example 264, 50 mg, 0.09 mmol) in methanol (5 mL) and stirred at RT for 1 hour, at which time solvents were removed and the residue was purified by normal phase chromatography on silica gel eluting with a gradient of methanol in methylene chloride to afford 15 mg of the title compound as a white solid.
MS (EI) (M+H)+ 520 for C22H21F3N7O3S (M−H) 518 for C22H19F3N7O3S;
1H NMR (DMSO-d6) δ: 9.53 (s, 1H), 9.21 (d, J=1.88 Hz, 1H), 8.72 (d, J=1.88 Hz, 1H), 8.57 (s, 1H), 8.42 (s, 1H), 8.33 (t, J=1.98 Hz, 1H), 8.24 (s, 1H), 7.57 (t, J=5.18 Hz, 1H), 5.96 (s, 1H), 3.21 (qd, J=7.16, 6.03 Hz, 2H), 1.60 (s, 6H), 1.11 (t, J=7.16 Hz, 3H);
19F-NMR (DMSO-d6) δ: −62.57 (s, 3 F);
A solution of triphenyl phosphine (55 mg, 0.2 mmol) and DIEA (0.15 ml) in acetonitrile (2 ml) was added to 1-(2-(6′-(3-ethylureido)-4′-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridine-5-carbonyl)hydrazinyl)-2-methyl-1-oxopropan-2-yl acetate (Intermediate 448, 50 mg, 0.1 mmol). The resulting solution was treated with carbontetrachloride (0.1 ml) and let stir at RT for 2 hours. Volatiles were removed under reduced pressure and the residue was purified by normal phase chromatography on silica gel eluting with a gradient of ethyl acetate in hexanes to afford 30 mg of the title compound as an off white solid.
MS (EI) (M+H)+ 562 for C24H23F3N7O4S (M−H)− 560 for C24H21F3N7O4S;
1H NMR (DMSO-d6) δ: 9.53 (s, 1H), 9.20 (br. s., 1H), 8.73 (br. s., 1H), 8.57 (s, 1H), 8.42 (s, 1H), 8.32 (br. s., 1H), 8.22 (s, 1H), 7.45-7.70 (m, 1H), 3.14-3.28 (m, 2H), 2.04 (s, 3H), 1.79 (s, 6H), 1.11 (t, J=7.06 Hz, 3H);
19F-NMR (DMSO-d6) δ: −62.61 (s, 3 F);
The following Examples were prepared according to the procedure for Example 264 using the starting materials indicated in the table.
Hydrochloric acid (3 ml, 1M in 1,4-dioxane) was added to a solution of (R)-tert-butyl 145-(6′-(3-ethylureido)-4′-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridin-5-yl)-1,3,4-oxadiazol-2-yl)-2-methylpropylcarbamate (Intermediate 468, 75 mg, 0.12 mmol) in 1,4-dioxane (10 mL) and methanol (5 ml), warmed to 50° C. for 1 hour, solvent was removed and the residue was precipitated from methanol with ethyl acetate to afford 50 mg of the HCl salt of the title compound as a white solid.
MS (EI) (M+H)+ 533 for C23H26F3N8O3S (M−H)− 531 for C23H24F3N8O3S;
1H NMR (DMSO-d6) δ: 9.57 (s, 1H), 9.23 (d, J=2.07 Hz, 1H), 9.00 (d, J=1.51 Hz, 3H), 8.77 (d, J=2.07 Hz, 0H), 8.60 (s, 0H), 8.42 (s, 0H), 8.34 (t, J=1.88 Hz, 0H), 8.26 (s, 1H), 7.52-7.61 (m, 0H), 4.74 (d, J=4.52 Hz, 1H), 3.17-3.27 (m, 2H), 2.33-2.43 (m, 1H), 1.11 (1, J=7.25 Hz, 3H), 1.06 (d, J=6.78 Hz, 3H), 0.94 (d, J=6.78 Hz, 3H);
19F-NMR (DMSO-d6) δ: −62.60 (s, 3 F);
A solution of (9H-fluoren-9-yl)methyl (5-(6′-(3-ethylureido)-4′-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridin-5-yl)-1,3,4-oxadiazol-2-yl)methylcarbamate (Example 269, 40 mg, 0.06 mmol) in 1,4-dioxane (10 mL) was treated with piperidine (2 mL, 0.06 mmol), and stirred for 1 hour at room temperature, solvents were removed under reduced pressure. The residue was dissolved in methanol (5 ml) and treated with HCl (4 M in dioxane, 0.4 ml), the solution was diluted with ethyl acetate and the resulting solid was isolated by filtration to afford the HCl salt of the title compound as a white solid.
MS (EI) (M+H)+ 491 for C20H18F3N8O2S (M−H)− 489 for C20H16F3N8O2S;
1H NMR (DMSO-d6) δ: 9.66 (br. s., 1H), 9.22 (s, 1H), 8.97 (br. s., 3H), 8.75 (d, J=1.88 Hz, 1H), 8.60 (s, 1H), 8.41 (s, 1H), 8.38 (d, J=1.70 Hz, 1H), 8.29 (s, 1H), 7.63 (br. s., 1H), 4.51 (d, J=5.09 Hz, 2H), 3.17-3.29 (m, 2H), 1.17 (t, J=6.97 Hz, 3H);
19F-NMR (DMSO-d6) δ: −62.56 (s, 3 F)
Potassium carbonate (200 mg, 1.45 mmol) was added to a solution of 1-(5′-(2-(2-chloroacetyl)hydrazinecarbonyl)-4-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridin-6-yl)-3-ethylurea (Intermediate 464, 130 mg, 0.25 mmol) in DMF (3 ml) and the resulting solution was heated to 60° C. for 210 minutes. The reaction was then diluted with ethyl acetate (50 ml), water (20 ml), and saturated ammonium chloride (40 ml). The layers separated and the aqueous phase extracted with ethyl acetate (2×50 ml). The combined organics were washed with brine, dried over magnesium sulfate, filtered, and the solvents removed under reduced pressure. The resulting residue was purified by normal phase chromatography on silica gel eluting with a gradient of methanol in methylene chloride to give 26 mg of the title compound as a white powder.
MS (EI) (M+H)+ 492 for C20H17F3N7O3S (M−H) 490 for C20H15F3N7O3S;
1H NMR (DMSO-d6) δ: 11.19 (s, 1H), 9.49 (s, 1H), 8.95 (br. s., 1H), 8.56 (br. s., 2H), 8.34 (s, 1H), 8.22 (s, 1H), 8.03 (br. s., 1H), 7.57 (br. s., 1H), 4.80 (s, 2H), 3.12-3.27 (m, 2H), 1.10 (t, J=6.97 Hz, 3H);
19F-NMR (DMSO-d6) δ: −62.45 (s, 3 F)
A solution of 1-ethyl-3-(5′-(hydrazinecarbonyl)-4-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridin-6-yl)urea (Intermediate 9, 250 mg, 0.55 mmol), 1,1-dimethoxy-N,N-dimethylethanamine (0.5 mL, 0.55 mmol) in methanol (5 mL), was stirred at RT for 17 hours, hydrazine (0.2 mL, 0.55 mmol) was added and the suspension was stirred at RT for 10 hours, a small amount of insoluble material was removed by filtration. The filtrate was concentrated under reduced pressure and the residue was purified by normal phase chromatography on silica gel eluting with a gradient of methanol in dichloromethane to give 60 mg of the title compound as a tan solid.
MS (EI) (M+H)+ 490 for C20H19F3N9OS (M−H)− 488 for C20H17F3N9OS;
1H NMR (DMSO-d6) δ: 9.51 (s, 1H), 9.23 (d, J=1.88 Hz, 1H), 8.59 (d, J=2.07 Hz, 1H), 8.56 (s, 1H), 8.34-8.41 (m, 2H), 8.26 (s, 1H), 7.60 (t, J=5.18 Hz, 1H), 6.06 (s, 2H), 3.14-3.27 (m, 2H), 2.38 (s, 3H), 1.11 (t, J=7.16 Hz, 3H);
19F-NMR (DMSO-d6) δ: −62.35 (s, 3 F)
To a nitrogen-purged mixture of 1-(5-bromo-4-(4-phenylthiazol-2-yl)pyridin-2-yl)-3-ethylurea (Intermediate 16, 125 mg, 0.31 mmol) in DME (3 mL) were added pyrimidin-5-ylboronic acid (46.1 mg, 0.37 mmol), sodium bicarbonate (52.1 mg, 0.62 mmol) and water (1 mL), followed by tetrakis(triphenylphosphine)palladium(0) (71.6 mg, 0.06 mmol). The mixture was microwaved for 60 min at 110° C. The solvent was evaporated from the reaction mixture. The crude mass was washed with ethyl acetate and purified on reverse phase preparative HPLC to yield pure 1-ethyl-3-(4-(4-phenylthiazol-2-yl)-5-(pyrimidin-5-yl)pyridin-2-yl)urea (28.0 mg, 22.45%) as white solid powder.
MS (ES+): 402.9 for C21H18N6OS
1H NMR δ(DMSO D6): 1.1 (t, 3H), 3.2 (qn, 2H), 7.29-7.43 (m, 3H), 7.58 (t, 1H), 7.70 (d, 2H), 8.23 (s, 2H), 8.35 (s, 1H), 8.80 (s, 2H), 9.20 (s, 1H), 9.48 (s, 1H)
To a nitrogen-purged mixture of 1-(5-bromo-4-(4-phenylthiazol-2-yl)pyridin-2-yl)-3-ethylurea (Intermediate 16, 125 mg, 0.31 mmol) in DME (3 mL) were added 2-methoxypyrimidin-5-ylboronic acid (57.3 mg, 0.37 mmol), sodium bicarbonate (52.1 mg, 0.62 mmol) and water (1 mL), followed by tetrakis(triphenylphosphine)palladium(0) (71.6 mg, 0.06 mmol). The resulting mixture was microwaved for 60 min at 110° C. The solvent was evaporated from the reaction mixture, and the crude mass was washed with ethyl acetate and purified on reverse phase preparative HPLC to yield pure 1-ethyl-3-(5-(2-methoxypyrimidin-5-yl)-4-(4-phenylthiazol-2-yl)pyridin-2-yl)urea (40.0 mg, 29.8%) as white solid powder.
MS (ES+): 432.8 for C22H20N6O2S
1H NMR δ(DMSO D6): 1.1 (t, 3H), 3.2 (qn, 2H), 4.0 (s, 3H), 7.32-7.45 (m, 3H), 7.61 (t, 1H), 7.78 (d, 2H), 8.24 (s, 1H), 8.27 (s, 1H), 8.30 (s, 1H), 8.61 (s, 2H), 9.40 (s, 1H)
To a nitrogen-purged mixture of 1-(5-bromo-4-(4-phenylthiazol-2-yl)pyridin-2-yl)-3-ethylurea (Intermediate 16, 125 mg, 0.31 mmol) in DME (3 mL) were added 6-fluoropyridin-3-ylboronic acid (65.5 mg, 0.46 mmol), sodium bicarbonate (52.1 mg, 0.62 mmol) and water (1 mL), followed by tetrakis(triphenylphosphine)palladium(0) (71.6 mg, 0.06 mmol). The resulting mixture was microwaved for 60 min at 110° C. When LCMS indicated that the required product had formed and absence of starting material, the solvent was evaporated from the reaction mixture. The crude mass was washed with ethyl acetate and purified on reverse phase preparative HPLC to yield pure 1-ethyl-3-(6′-fluoro-4-(4-phenylthiazol-2-yl)-3,3′-bipyridin-6-yl)urea (45.0 mg, 34.6%).
MS (ES+): 419.8 for C22H18FN5OS
1H NMR δ(DMSO D6): 1.1 (t, 3H), 3.2 (qn, 2H), 7.24-7.28 (m, 1H), 7.33-7.45 (m, 3H), 7.64 (t, 1H), 7.77-7.80 (m, 2H), 7.93-8.0 (m, 1H), 8.22-8.25 (m, 2H), 8.27 (d, 2H), 9.42 (b, 1H)
A mixture of (1-(4-bromo-5′-(5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)-3,3′-bipyridin-6-yl)-3-ethylurea (Intermediate 470, 54 mg, 0.13 mmol), 4-(2-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol-1-yl)ethyl)morpholine (43.0 mg, 0.14 mmol), K2CO3 (27.6 mg, 0.20 mmol) and tetrkis(triphenylphosphine)palladium (0) (15.40 mg, 0.01 mmol) was suspended in DMF (3.5 ml)/water (0.1 ml) in a microwave reaction vassel, purged with N2 and heated under microwave at 95° C. for 2 hours. The crude sample was filtered through celite and the filtrate was concentrated and purified by column chromatography on silica gel, eluted with 10% methanol in dichloromethane to give the desired product (25 mg).
MS (ESP) 428.2 (MH+) for C24H27N9O4.
1H-NMR (DMSO-d6): 1.10 (t, 3H); 2.32 (m, 2H); 2.38 (m, 2H); 2.59 (m, 1H); 2.68 (t, 1H); 3.21 (t, 1H); 3.45-3.55 (m, 4H); 4.13-4.24 (m, 3H); 7.03 (s, 1H); 7.18 (s, 1H); 7.63 (t, 1H); 7.72 (t, 1H); 7.97 (s, 1H); 8.17 (s, 1H); 8.58 (d, 1H); 8.95 (s, 1H); 9.31 (s, 1H); 12.80 (br, 1H).
1-Ethyl-3-(4-ethynyl-5′-(5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)-3,3′-bipyridin-6-yl)urea (Intermediate 475, 45 mg, 0.13 mmol), 2,6-lutidine (0.022 ml, 0.19 mmol), copper (I) iodide (2.446 mg, 0.01 mmol) and (azidomethyl)benzene (18.19 mg, 0.13 mmol) were mixed in acetonitrile (10 ml) and NMP (1 ml) and stirred at 65° C. overnight. The reaction mixture was diluted with DCM and filtered through membrane. The filtrate was concentrated and purified by ISCO column (silica gel) eluted with MeOH/DCM (10:1), and then purified again with Gilson (C-18 column, 10%˜85% MeCN in H2O, 0.1% TFA) to give the desired product as a white solid (10 mg).
MS (ESP) 484 (MH+) for C24H21N9O3
1H-NMR (DMSO-d6): 1.10 (t, 3H); 3.20 (m, 2H); 5.51 (s, 2H); 7.15 (m, 2H); 7.27 (m, 3H); 7.72 (m, 1H); 7.87 (m, 2H); 7.98 (s, 1H); 8.24 (s, 1H); 8.62 (d, 1H); 8.94 (d, 1H); 9.42 (s, 1H); 12.82 (br, 1H).
2N LiOH (1 mL) was added to a mixture of ethyl 6′-{[(ethylamino)carbonyl]amino}-4′-[4-(trifluoromethyl)-1,3-thiazol-2-yl]-3,3′-bipyridine-5-carboxylate (Intermediate 2, 0.385 g, 0.83 mmol) in MeOH (3 mL) and THF (3 mL). The resulting solution was stirred at room temperature for two hours. The solvent was removed and the residue was diluted with water and acidified with 1N HCl. The precipitated product was collected by filtration and washed with water and dried (0.297 g).
MS (ES) MH+: 437 for C18H14F3N5O3S;
1H-NMR (DMSO-d6) δ: 1.11 (t, 3H); 3.18-3.24 (m, 2H); 7.57 (brs, 1H); 8.15-8.18 (m, 1H); 8.22 (s, 1H); 8.37 (s, 1H); 8.57 (s, 1H); 8.72 (s, 1H); 9.08 (s, 1H); 9.51 (s, 1H); 13.53 (s, 1H)
1-(5-Bromo-4-(4-(trifluoromethyl)thiazol-2-yl)pyridin-2-yl)-3-ethylurea (Intermediate 3, 500 mg, 1.27 mmol), cesium carbonate (618 mg, 1.90 mmol), tetrakis(triphenylphosphine)palladium(0) (146 mg, 0.13 mmol), ethyl 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)nicotinate (526 mg, 1.52 mmol) were taken in a microwave vial and degassed with Argon. Then dioxane:water (4:1, 8 mL) was added to it and microwaved at 100° C. for half an hour. The reaction mixture was partitioned between water and ethyl acetate and layers separated. The organic layer was washed with saturated sodium bicarbonate solution, water, brine and dried over magnesium sulfate. The solvent was removed and the residue was purified by flash chromatography eluting with 2% MeOH in dichloromethane to 3% MeOH in dichloromethane to give 330 mg of the title compound.
MS (ES) MH+: 466 for C20H18F3N5O3S;
1H-NMR (DMSO-d6) δ: 1.11 (t, 3H); 1.31 (t, 3H); 3.18-3.24 (m, 2H); 4.34 (q, 2H); 7.57 (brs, 1H); 8.16-8.18 (m, 1H); 8.21 (s, 1H); 8.39 (s, 1H); 8.58 (s, 1H); 8.75 (d, 1H); 9.10 (s, 1H); 9.52 (s, 1H).
TFAA (1.128 mL, 7.99 mmol) followed by TEA (1.113 mL, 7.99 mmol) were added to a mixture of 1-(5-bromo-4-(4-hydroxy-4-(trifluoromethyl)-4,5-dihydrothiazol-2-yl)pyridin-2-yl)-3-ethylurea (Intermediate 4, 2.2 g, 5.32 mmol) in DCM (30 mL). The reaction mixture was allowed to stir overnight at room temperature. Another 150 uL of TEA and TFAA were added and the reaction mixture was stirred for additional 3 h. Then the reaction was concentrated under reduced pressure and the residue was partitioned between water and ethyl acetate. The layers were separated and the organic layer was washed with sodium bicarbonate solution, water and brine. The organic layer was dried over magnesium sulfate and concentrated under reduced pressure. The light yellow solid obtained was purified by normal phase chromatography (1% MeOH in dichloromethane to 3% MeOH in dichloromethane) to give the desired product (617 mg). MS (ESP): 396 (M+1) for C12H10BrN3O; NMR: 1.07 (t, 3H); 3.11-3.17 (m, 2H); 7.24 (t, 1H); 8.35 (s, 1H); 8.50 (s, 1H); 8.77 (s, 1H); 9.34 (s, 1H).
Intermediate 4
To a mixture of 5-bromo-2-(3-ethylureido)pyridine-4-carbothioamide (Intermediate 5, 1.1 g, 3.63 mmol) in acetonitrile (25 mL), was added 3-bromo-1,1,1-trifluoropropan-2-one (2.260 mL, 21.77 mmol) and the reaction mixture was heated at 80° C. for 4 h. A clear solution resulted within an hour. The solution was then concentrated under reduced pressure and the resulting residue was partitioned between water and ethyl acetate. The organic layer was washed with water and brine, dried over magnesium sulfate and concentrated under reduced pressure to give light yellow solid, which, was purified by normal phase column chromatography (silica, 2% MeOH in dichloromethane to 5% MeOH in dichloromethane) to give white solid (470 mg). MS (ESP): 414 (M+1) for C12H12BrF3N4O2S; NMR: 1.06 (t, 3H); 3.12-3.18 (m, 2H); 3.60 (dd, 1H); 3.90 (dd, 1H); 7.13 (brs, 1H); 7.98 (s, 1H); 8.47 (s, 1H); 9.41 (s, 1H).
To a mixture of 5-bromo-2-(3-ethylureido)isonicotinamide (Intermediate 6, 1.25 g, 4.35 mmol) in THF (20 mL), was added Lawessons reagent (1.761 g, 4.35 mmol). The reaction mixture was then heated to 70° C. overnight. The solid that formed was collected by filtration and washed with THF to provide 1 g of desired product. MS (ESP): 304 (M+1) for C19H11BrN4OS
To a mixture of methyl 2-amino-5-bromoisonicotinate (3 g, 12.98 mmol) and chloroform (12 mL) in a microwave vial, isocyanatoethane (1.122 mL, 14.28 mmol) was added and the reaction mixture was heated at 110° C. for 3 h. The reaction mixture was concentrated under reduced pressure and 50 mL of 7N ammonia in MeOH was added. The resulting mixture was stirred at room temperature overnight, concentrated under reduced pressure and the resulting solid obtained was washed with acetonitrile to give a white solid (3.5 g).
MS (ESP): 287 (M+1) for C19H11BrN4O2
Triethylamine (0.054 mL, 0.39 mmol) and acetohydrazide (14.40 mg, 0.19 mmol) were added to a solution of 6′-(3-ethylureido)-4′-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridine-5-carboxylic acid (Intermediate 1, 85 mg, 0.19 mmol) in DMF (1.5 mL). The mixture was stirred for 5 minutes and then HATU (89 mg, 0.23 mmol) was added. The resulting light yellow solution was stirred at room temperature for one hour then it was diluted with water. The aqueous layer was freeze dried and the solid obtained was extracted with THF and concentrated to give 184 mg of the crude product.
MS (ESP): 494 (M+1) for C20H18F3N7O3S
Intermediate 9 was synthesized according to the procedure described for Intermediate 7 using 6′-(3-ethylureido)-4′-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridine-5-carboxylic acid and isobutylhydrazide as the starting material.
MS (ESP): 522 (M+1) for C22H22F3N7O3S
1H-NMR (DMSO-d6) δ: 1.06 (d, 6H); 1.10 (t, 3H); 3.12-3.27 (m, 3H); 7.54 (brs, 1H); 8.19 (s, 1H); 8.24 (s, 1H); 8.36 (s, 1H); 8.56 (s, 1H); 8.64 (d, 1H); 9.04 (d, 1H); 9.49 (s, 1H); 9.94 (s, 1H); 10.54 (s, 1H).
Ethyl 6′-(3-ethylureido)-4′-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridine-5-carboxylate (Intermediate 2, 150 mg, 0.32 mmol) and hydrazine hydrate (31 mg, 0.97 mmol) were taken in ethanol (6 ml) and heated at 80° C. for 5 h. The reaction was cooled down and concentrated to give tan colored solid that was washed with 10% MeOH in dichloromethane and dried to give the title compound (101 mg).
MS (ESP): 452 (M+1) for C18H16F3N7O3S
1H-NMR (DMSO-d6) δ: 1.09 (t, 3H); 3.10-3.25 (m, 2H); 4.57 (brs, 2H); 7.55 (brs, 1H); 8.13 (s, 1H); 8.23 (s, 1H); 8.34 (s, 1H); 8.55 (s, 1H); 8.59 (s, 1H); 8.99 (s, 1H); 9.48 (s, 1H); 9.97 (s, 1H).
A mixture of 6′-(3-ethylureido)-4′-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridine-5-carboxamide (Intermediate 11, 270 mg, 0.62 mmol) in 1,1-dimethoxy-N,N-dimethylethanamine (10 mL, 68.40 mmol) was heated to 120° C. for one hour and cooled down. The solid was filtered off and washed with acetonitrile and dried to give product as off-white solid (178 mg).
MS (ESP): 506 (M+1) for C22H22F3N7O2S
1H-NMR (DMSO-d6) δ: 1.10 (t, 3H); 2.29 (s, 3H); 3.11 (s, 3H); 3.14 (s, 3H); 3.15-3.28 (m, 2H); 7.60 (brs, 1H); 8.14 (s, 1H); 8.20 (s, 1H); 8.37 (s, 1H); 8.55 (s, 1H); 8.63 (d, 1H); 9.16 (d, 1H); 9.48 (s, 1H).
Triethylamine (0.040 mL, 0.29 mmol) and 2-phenylpropan-2-amine (19.47 mg, 0.14 mmol) were added to a solution of 6′-(3-ethylureido)-4′-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridine-5-carboxylic acid (Intermediate 1, 63 mg, 0.14 mmol) in DMF (1.5 mL). The reaction solution was stirred for 5 minutes and then 2-(3H-[1,2,3]triazolo[4,5-b]pyridin-3-yl)-1,1,3,3-tetramethylisouronium hexafluorophosphate(V) (54.8 mg, 0.14 mmol) were added. The resulting light yellow solution was stirred at room temperature for 30 min. The desired product was precipitated with water and collected via filtration and dried to give an off-white solid (62 mg). The precipitate was taken in TFA (2 mL) and stirred overnight at room temperature and at 40° C. for another 3 h. The reaction was concentrated under reduced pressure and the residue was taken up in ethyl acetate and washed with sodium bicarbonate solution, water and brine. It was then dried over magnesium sulfate and concentrated to give white solid that was triturated with acetonitrile and dried to give the product (33 mg).
MS (ESP): 437 (M+1) for C18H15F3N6O2S
1H-NMR (DMSO-d6: 1.09 (t, 3H); 3.18-3.24 (m, 2H); 7.45 (br s, 1H); 7.65 (s, 1H); 8.16 (s, 1H); 8.18 (s, 1H); 8.24 (s, 1H); 8.35 (s, 1H); 8.55 (d, 1H); 8.60 (d, 1H); 9.05 (s, 1H); 9.49 (s, 1H).
1-(5-Bromo-4-(4-(trifluoromethyl)thiazol-2-yl)pyridin-2-yl)-3-ethylurea (Intermediate 3, 200 mg, 0.51 mmol), 4,4,4′,4′,5,5,5′,5′-octamethyl-2,2′-bi(1,3,2-dioxaborolane) (386 mg, 1.52 mmol), potassium acetate (149 mg, 1.52 mmol), and 1,1′-bis(diphenylphosphino)ferrocene-palladium dichloride (20.72 mg, 0.03 mmol) were taken in a microwave vial and degassed with argon. DMSO (4 mL) was added to the vial and the solution was heated at 90° C. for 5 h. The reaction mixture was partitioned between water and ethyl acetate. The layers were separated and the organic layer was back extracted three times with ethyl acetate. The organic layers were combined and washed with water and brine, then dried over magnesium sulfate and concentrated under reduced pressure to give a light brown solid that was a mixture of the title compound (35%), {6-{[(ethylamino)carbonyl]amino}-4-[4-(trifluoromethyl)-1,3-thiazol-2-yl]pyridin-3-yl}boronic acid (25%) and N-ethyl-N-{4-[4-(trifluoromethyl)-1,3-thiazol-2-yl]pyridin-2-yl}urea (25%). The crude mixture was taken to the next step without further purification.
In a microwave reaction vessel, 1-ethyl-3-(5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-4-(4-(trifluoromethyl)thiazol-2-yl)pyridin-2-yl)urea (Intermediate 12, 415 mg, 0.94 mmol), methyl 2-bromothiazole-5-carboxylate (208 mg, 0.94 mmol) and cesium carbonate (119 mg, 1.13 mmol) were combined and suspended in dioxane/water. Pd(PPh3)4 (54.2 mg, 0.05 mmol) was added in a single portion. The vessel was sealed and heated to 100° C. in the microwave for 60 minutes, then diluted with water and EtOAc. The aqueous and organic layers were separated, and the organic was dried over Na2SO4, filter and concentrate. Solids precipitated from solution upon concentrating and were collected and washed with minimal CH2Cl2. Analysis showed the solids to the desired reaction product. The mother liquor was concentrated further and the crude product was purified by flash column chromatography (0-100% EtOAc/hexanes). Isolation gave 128 mg of the title compound.
MS (ESP): 458 (M+1) for C17H14F3N5O3S2.
Intermediate 14
Isocyanatoethane (0.913 mL, 11.56 mmol) was added to a mixture of 4-bromopyridin-2-amine (2 g, 11.56 mmol) in chloroform (10 mL), and the mixture was heated at 110° C. for 2 h. The reaction mixture was concentrated under reduced pressure and triturated with acetonitrile to give a white solid (2.15 g).
MS (ESP): 243 (M+1) for C8H10BrN3O
1H-NMR (DMSO-d6) δ: 1.08 (t, 3H); 3.12-3.18 (m, 2H); 7.16 (dd, 1H); 7.65 (brs, 1H); 7.74 (s, 1H); 8.07 (d, 1H); 9.29 (s, 1H)
2-Bromo-1-pyridin-2-ylethanone (0.463 g, 1.65 mmol) was added to a mixture of 5-bromo-2-(3-ethylureido)pyridine-4-carbothioamide (Intermediate 5, 0.5 g, 1.65 mmol) in acetonitrile (3 mL), and the reaction mixture was heated to 80° for six hours. The reaction mixture was cooled to room temperature and concentrated under reduced pressure. The crude reaction mixture was purified by column chromatography (Silica gel, 10% MeOH in CH2Cl2).
Isolation gave 670 mg of the title compound as an off-white solid. LC/MS (ES+)[(M+H)+]: 404, 406 for C16H14BrN5OS.
1H NMR (300 MHz, d6-DMSO): 1.08 (t, 3H), 3.18 (m, 2H), 7.33 (t, 1H), 7.42 (m, 1H), 7.98 (m, 1H), 8.16 (m, 1H), 8.51 (s, 1H), 8.55 (s, 1H), 8.59 (s, 1H), 8.67 (s, 1H), 9.39 (s, 1H).
2-Bromo-1-phenylethanone (0.105 g, 0.53 mmol) was added to a mixture of 5-bromo-2-(3-ethylureido)pyridine-4-carbothioamide (Intermediate 5, 0.146 g, 0.48 mmol) in acetonitrile (3 mL), and the reaction mixture was heated to 80° for 16 h. The reaction mixture was cooled to room temperature and concentrated under reduced pressure. The resulting solids were filtered and washed with acetonitrile. Isolation gave 164 mg of the title compound as an off-white solid.
LC/MS (ES+)[(M+H)+]: 403, 405 for C17H15BrN4OS.
1H NMR (300 MHz, d6-DMSO): 1.08 (t, 3H); 3.04-3.28 (m, 2H); 7.36 (m, 1H); 7.45 (m, 1H); 7.50 (t, 2H); 8.02-8.10 (m, 2H); 8.47 (s, 1H); 8.50 (s, 1H); 8.53 (s, 1H); 9.39 (s, 1H).
Intermediate 17
1-(4-bromopyridin-2-yl)-3-ethylurea (Intermediate 14, 0.50 g, 2.05 mmol), copper(I) iodide (0.039 g, 0.20 mmol), and Pd(PPh3)4 (0.118 g, 0.10 mmol) were combined in a microwave vial and degassed with nitrogen. DMF (4 mL) was added to the vial followed by slow addition of 2-(tributylstannyl)benzo[d]thiazole (1.130 g, 2.66 mmol), and the reaction mixture was heated to 100° C. for 60 minutes. The reaction mixture was partitioned between water and ethyl acetate and layers separated. The organic layer was washed with saturated NaHCO3, water, brine and dried over magnesium sulfate, and concentrated. The resulting solids were filtered and then washed with acetonitrile followed by chloroform to yield 140 mg of the title compound as an off-white solid.
LC/MS (ES+)[(M+H)+]: 299 for C15H14N4OS.
1H NMR (300 MHz, d6-DMSO): 1.11 (t, 3H), 3.21 (m, 2H), 7.54 (t, 1H), 7.56 (d, 1H), 7.61 (m, 1H), 7.76 (t, 1H), 8.15 (d, 1H), 8.21 (d, 1H), 8.23 (s, 1H), 8.35 (d, 1H), 9.39 (s, 1H).
In a 25 mL pear-shaped flask 1-(4-(benzo[d]thiazol-2-yl)pyridin-2-yl)-3-ethylurea (Intermediate 17, 144 mg, 0.48 mmol) and 1-bromopyrrolidine-2,5-dione (96 mg, 0.54 mmol) were suspended in DMF (2 mL). The reaction mixture was heated to 80° C. for 4 hrs. The reaction was partitioned between water and ethyl acetate. The layers were separated and the organic layer was washed with a 5% sodium thiosulfate solution, followed by water and brine, then dried over magnesium sulfate and concentrated. The solids were tichurated with acetonitrile, filtered, washed and dried in vacuo. Isolation gave 160 mg of the title compound as an off-white solid.
LC/MS (ES+)[(M+H)+]: 377, 379 for C18H13BrN4OS.
1H NMR (300 MHz, d6-DMSO): 1.09 (t, 3H), 3.17 (m, 2H), 7.27 (t, 1H), 7.58 (t, 1H), 7.65 (t, 1H), 8.19 (d, 1H), 8.27 (d, 1H), 8.42 (s, 1H), 8.58 (s, 1H), 9.44 (s, 1H).
In a microwave vessel, N-[5-bromo-4-(4-pyridin-2-yl-1,3-thiazol-2-yl)pyridin-2-yl]-N′-ethylurea (Intermediate 15, 0.1 g, 0.25 mmol), ethyl 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)nicotinate (0.103 g, 0.37 mmol) and cesium carbonate (0.121 g, 0.37 mmol) were combined and suspended in a mixture of dioxane and water (4:1; 2.5 mL/0.5 mL). The suspension was degassed and purged with nitrogen. Pd(PPh3)4 (0.014 g, 0.01 mmol) was added and the mixture was degassed and purged a second time. The reaction mixture was heated in the microwave at 100° C. for 60 minutes. The reaction was partitioned between water and ethyl acetate. The layers were separated, and the organic phase was washed with saturated NaHCO3, water and brine, then dried over magnesium sulfate and concentrated. The resulting solids were filtered, then washed with acetonitrile followed by chloroform. Isolation gave 80 mg of the title compound as an off-white solid.
LC/MS (ES+)[(M+H)+]: 475 for C24H22N6O3S.
1H NMR (300 MHz, CHCl3): 1.11 (t, 3H), 1.25 (t, 3H), 3.21 (m, 2H), 4.29 (m, 2H), 7.35 (m, 1H), 7.60 (s, 1H), 7.63 (s, 1H), 7.82 (m, 1H), 8.26 (m, 2H), 8.34 (s, 1H), 8.36 (s, 1H), 8.60 (m, 1H), 8.80 (d, 1H), 9.10 (d, 1H), 9.49 (s, 1H).
In a microwave vessel, N-[5-bromo-4-(4-phenyl-1,3-thiazol-2-yl)pyridin-2-yl]-N′-ethylurea (Intermediate 16, 0.17 g, 0.42 mmol), ethyl 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)nicotinate (0.14 g, 0.51 mmol) and cesium carbonate (0.165 g, 0.51 mmol) were combined and suspended in a mixture of dioxane and water (4:1; 2.5 mL/0.5 mL). The suspension was degassed and purged with nitrogen. Pd(PPh3)4 (0.024 g, 0.02 mmol) was added and the mixture was degassed and purged a second time. The reaction mixture was heated in the microwave at 100° C. for 60 minutes. The reaction was partitioned between water and ethyl acetate, the layers were separated, and the organic phase was washed with saturated NaHCO3, water and brine, then dried over magnesium sulfate, and concentrated. The resulting solids were filtered, washed with acetonitrile followed by chloroform. Isolation gave 200 mg of the title compound as an off-white solid.
LC/MS (ES+)[(M+H)+]: 474 for C25H23N5O3S;
1H NMR (300 MHz, CHCl3): 1.10 (t, 3H), 1.26 (t, 3H), 3.21 (m, 2H), 4.30 (q, 2H), 7.25 (t, 1H), 7.63 (t, 1H), 7.35 (s, 1H), 7.38 (s, 1H), 7.68 (d, 1H), 7.71 (d, 1H), 8.22 (s, 1H), 8.24 (s, 1H), 8.26 (t, 1H), 8.32 (t, 1H), 8.77 (d, 1H); 9.10 (d, 1H), 9.48 (s, 1H).
Intermediate 21 was synthesized as described for Intermediate 20 from Intermediate 18 and ethyl 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)nicotinate.
LC/MS (ES+)[(M+H)+]: 448 for C23H21N5O3S.
1H NMR (300 MHz, d6-DMSO): 1.11 (t, 3H), 1.25 (t, 3H), 3.21 (m, 2H), 4.29 (q, 2H), 7.47 (m, 1H), 7.54 (m, 1H), 7.60 (t, 1H), 7.98 (m, 1H), 8.09 (m, 1H), 8.24 (t, 1H), 8.27 (s, 1H), 8.41 (s, 1H), 8.74 (d, 1H), 9.07 (d, 1H), 9.54 (s, 1H).
In a 25 mL round-bottom flask, ethyl 6′-{[(ethylamino)carbonyl]amino}-4′-(4-pyridin-2-yl-1,3-thiazol-2-yl)-3,3′-bipyridine-5-carboxylate (Intermediate 19, 0.26 g, 0.55 mmol) and hydrazine hydrate (0.165 g, 3.29 mmol) were mixed in ethanol (6 mL), and stirred at 80° C. overnight. The reaction mixture was cooled to room temperature and concentrated under reduced pressure. The resulting residue was tichurated with 10% MeOH in DCM. The resulting solid was filtered, washed and dried in vacuo. Isolation gave 250 mg of the title compound.
LC/MS (ES+)[(M+H)+]: 461 for C22H20N8O2S.
1H NMR (300 MHz, d6-DMSO): 1.11 (t, 3H), 3.22 (m, 2H), 4.58 (s, 2H), 7.36 (m, 1H), 7.68 (s, 1H), 7.70 (s, 1H), 7.86 (m, 1H), 8.21 (t, 1H), 8.32 (s, 1H), 8.33 (s, 1H), 8.36 (s, 1H), 8.60 (m, 1H), 8.64 (d, 1H), 9.0 (d, 1H), 9.52 (s, 1H), 10.02 (s, 1H).
Intermediates 23 was synthesized according to the procedure described for Intermediate 22 from Intermediate 20 and hydrazine.
LC/MS (ES+)[(M+H)+]: 460 for C23H21N7O2S.
1H NMR (300 MHz, d6-DMSO): 1.12 (t, 3H), 3.22 (m, 2H), 4.58 (s, 2H), 7.34-7.43 (m, 3H), 7.64 (t, 1H), 7.74 (d, 1H), 7.76 (d, 1H), 8.20 (t, 1H), 8.23 (s, 1H), 8.28 (s, 1H), 8.32 (s, 1H), 8.63 (d, 1H), 9.01 (d, 1H), 9.48 (s, 1H), 10.01 (s, 1H).
Intermediates 24 was synthesized according to the procedure described for Intermediate 22 from Intermediate 21 and hydrazine
LC/MS (ES+)[(M+H)+]: 434 for C21H19N7O2S.
1H NMR (300 MHz, CHCl3): 1.10 (t, 3H), 3.16 (m, 2H), 4.55 (s, 2H), 7.48 (m, 1H), 7.54 (m, 1H), 7.57 (m, 1H), 7.98 (d, 1H), 8.09 (d, 1H), 8.18 (t, 1H), 8.28 (s, 1H), 8.38 (s, 1H), 8.58 (d, 1H), 8.97 (d, 1H), 9.52 (s, 1H), 9.98 (s, 1H).
A slurry of crude 1-ethyl-3-(5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-4-(4-(trifluoromethyl)thiazol-2-yl)pyridin-2-yl)urea (Intermediate 12, 110 mg, 0.25 mmol), diethyl 2-chlorothiazole-4,5-dicarboxylate (WO2006087543, 66 mg, 0.25 mmol) and K2CO3 (86 mg, 0.625 mmol) in 1,4-dioxane-water (8+3 ml) was purged with nitrogen for 30 min at room temperature. Bis(triphenylphosphine)palladium dichloride (18 mg, 0.025 mmol) was added and the resulting mixture was stirred at 80-90° C. for 1.2 h. The reaction mixture was cooled, diluted with water (10 mL), and extracted with EtOAc (2×80 mL). The combined extracts were dried over sodium sulfate and concentrated to a residue under reduced pressure. The residue was purified via flash chromatography (50% EtOAc-heptane+10% EtOH) to afford 90 mg (67%) of desired product as light brown gum.
MS (ESP): 544 (M+H+) for C21H20F3N5O5S2
Hydrazine hydrate (0.110 mL, 3.49 mmol) was added to a mixture of methyl 3-(5-bromopyridin-3-yl)-3-oxopropanoate (300 mg, 1.16 mmol) in methanol (5 mL). The resulting mixture was heated at reflux for 2 h. The reaction mixture was cooled to room temperature and the solid that formed was collected by filtration. The solid was washed with methanol and dried under vacuum to give the title compound as an off-white solid.
MS (ESP): 239 (M−1) for C8H6BrN3
1H-NMR (DMSO-d6) δ: 6.12 (brs, 1H); 8.32 (s, 1H); 8.60 (s, 1H); 8.90 (s, 1H); 9.88 (br s, 1H); 12.33 (br s, 1H).
Hydroxylamine (0.040 mL, 0.65 mmol) (50% in water) was added to a suspension of 1-(5′-cyano-4-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridin-6-yl)-3-ethylurea (Example 2, 180 mg, 0.43 mmol) in ethanol (10 mL), and the mixture was heated to 80° C. for 1.5 hours. The reaction mixture was concentrated under reduced pressure and the resulting residue was triturated with acetonitrile to give the title compound as a tan colored solid (180 mg).
MS (ESP): 452 (M+1) for C19H14F3N7O3S
In a 25 mL flask, 1-(1-methyl-1H-pyrazol-4-yl)ethanone (0.602 g, 4.85 mmol) was dissolved in chloroform (20 mL). The colorless solution was made acidic with the addition of a few drops of HBr in acetic acid (3.92 mg, 0.05 mmol). A chloroform solution containing Br2 (0.262 mL, 5.09 mmol) was added dropwise via an addition funnel. The reaction mixture was stirred at room temperature for 1 h, and then concentrated under reduced pressure. The crude solid was triturated in ethyl acetate, filtered, and dried in vacuo. The free base was obtained by triturating the product in 5% NaHCO3 for 2 h. The solid was collected by filtration, washed with water, isopropyl alcohol and then dried in vacuo. Isolation gave 874 mg of the title compound.
LC/MS (ES+)[(M+H)+]: 204 for C6H7BrN2O.
1H NMR (300 MHz, d6-DMSO): 3.88 (s, 3H), 4.56 (s, 2H), 7.99 (s, 1H), 8.47 (s, 1H).
In a 25 mL flask 5-bromo-2-(3-ethylureido)pyridine-4-carbothioamide (Intermediate 5, 478 mg, 1.58 mmol) and 2-bromo-1-(1-methyl-1H-pyrazol-4-yl)ethanone (Intermediate 28, 352 mg, 1.73 mmol) were suspended in EtOH (10 mL). The reaction mixture was heated at 80° C. for 12 h. The reaction mixture was cooled to room temperature and concentrated under reduced pressure. The resulting solid was collected by filtration and washed with acetonitrile. Isolation gave 640 mg of the title compound as an off-white solid.
LC/MS (ES+)[(M+H)+]: 407, 409 for C15H15BrN6OS.
1H NMR (300 MHz, d6-DMSO): 1.08 (t, 3H), 3.18 (m, 2H), 3.9 (s, 3H), 7.34 (m, 1H), 7.91 (s, 1H), 8.03 (s, 1H), 8.17 (s, 1H), 8.41 (s, 1H), 8.52 (s, 1H), 9.37 (s, 1H).
The following Intermediate was prepared according to the procedure described for Intermediate 29 using the starting materials indicated.
In a pear-shaped flask, 1-(4-bromopyridin-2-yl)-3-ethylurea (Intermediate 14, 0.3 g, 1.23 mmol), 1-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole (0.281 g, 1.35 mmol), Pd2(dba)3 (0.113 g, 0.12 mmol), 2-dicyclohexylphosphino-2′,4′,6′-tri-iso-propyl-1,1′-biphenyl (0.176 g, 0.37 mmol), Na2CO3 (0.156 g, 1.47 mmol) were combined and suspended in a mixture of acetonitrile and water (5:1; 7 mL/1.4 mL). The suspension was degassed and purged with nitrogen. The reaction mixture was heated at 90° C. for 60 min., then concentrated under reduced pressure, and partitioned between water and ethyl acetate. The organic phase was washed with water and brine, and then dried over magnesium sulfate. The mother liquor was concentrated under reduced pressure. The resulting solid was filtered and washed with acetonitrile. Isolation gave 146 mg of the title compound as an off-white solid.
LC/MS (ES+)[(M+H)+]: 246 for C12H15N5O.
1H NMR (300 MHz, d6-DMSO): 1.08 (t, 3H), 3.19 (m, 2H), 3.9 (s, 3H), 6.53 (d, 1H), 7.11 (m, 1H), 7.51 (d, 1H), 7.56 (s, 1H), 7.97 (m, 1H), 8.26 (d, 1H), 9.26 (s, 1H).
The following intermediate was prepared in accordance to the procedure described for Intermediate 18 using the starting materials indicated in the table.
The following intermediates were prepared in accordance to the procedure described for Intermediate 20 using the starting materials indicated in the table.
The following intermediates were prepared in accordance to the procedure described for Intermediate 22 using the starting materials indicated in the table.
The following intermediates were prepared in accordance to the procedure described for Intermediate 20 using the starting materials indicated in the table.
Ethyl 2-amino-4-pyrimidin-2-yl-1,3-thiazole-5-carboxylate (Intermediate 47; 0.55 g, 2.2 mmol) was suspended in glacial acetic acid (20 ml) and concentrated HCl (30 ml). The solution was cooled to 0° C. and a solution of sodium nitrite in water (15 ml) was added dropwise. After stirring at 0° C. for 10 mins, the reaction was slowly warmed to room temperature and stirred for 1 hour. The reaction was monitored by LCMS and once complete, a solution of urea (0.25 g) in water (10 ml) was added dropwise. After stirring at room temperature for 30 mins, solvent was removed under reduced pressure. The residue was partitioned with sat. NaHCO3 (aq) and EtOAc. The layers were separated and the water layer was back extracted with EtOAc (×3). The combined organic layers were drying with MgSO4 and concentrating yielded an orange oil which was used without purification (0.20 g).
MS (ES) (M+H)+: 270 for C10H8ClN3O2S.
The following Intermediate was prepared according to the procedure described for Intermediate 43 from the starting materials indicated.
A suspension of ethyl 2-iodo-3-oxo-3-pyrimidin-2-ylpropanoate (Intermediate 47; 1.73 g, 5.4 mmol) and thiourea (0.62 g, 8.1 mmol) in EtOH was heated at reflux for 1 hour. After cooling to room temperature, the reaction was concentrated. The residue was suspended in water and basified with saturated aqueous Na2CO3. The resulting precipitate was filtered off and the filtrate was extracted with EtOAc (×3). The organic extracts were combined and dried with MgSO4, then concentrated to an orange oil (0.55 g, 41%).
MS (ES) (M+H)+: 251 for C10H10N4O2S
NMR: 0.97 (t, 3H), 3.95 (q, 2H), 7.55 (t, 1H), 7.94 (s, 1H), 8.85 (d, 1H), 9.05 (d, 1H).
The following Intermediate was synthesized according to the procedure described for Intermediate 45 from the starting materials indicated.
To a suspension of ethyl 3-oxo-3-pyrimidin-2-ylpropanoate (Intermediate 48; 1.19 g, 6.1 mmol) in EtOAc was added N-iodosuccinamide (1.38 g, 6.1 mmol) and Amberlyst-15 resin (1.19 g). After stirring at room temperature for 30 mins, LCMS shows a mixture of desired product and bis-iodinated product. The reaction mixture was filtered to remove the Amberlyst-15 resin, and the filtrate was concentrated to an orange oil which was then suspended in diethyl ether. The resulting precipitate was filtered and washed with ether. The filtrate was concentrated to an orange oil to provide the desired product (1.73 g, 89%).
MS (ES) (M+H)+: 321 for C9H9IN2O3
To a solution of pyrimidine-2-carboxylic acid (0.99 g, 7.98 mmol) in anhydrous THF (20 ml) was added carbonyl diimidazole (1.55 g, 9.57 mmol) and the suspension was heated at reflux for 2 hours. The mixture was then cooled to room temperature and used without workup or purification. In a separate flask, mono-ethyl malonate (0.94 ml, 7.98 mmol) was suspended in anhydrous THF (20 ml) and cooled to 0° C. Methyl magnesium bromide (5.32 ml, 15.96 mmol, 3.0 M in diethyl ether) was added dropwise. After stirring at 0° C. for 20 mins, the crude imidazolide solution prepared earlier was added slowly. The reaction was then heated at reflux overnight. After cooling to room temperature, the reaction mixture was diluted with water and acidified with concentrated HCl to pH 5. The solution was extracted with EtOAc (×3), dried with MgSO4 and concentrated to a yellow oil (1.19 g, 77%). NMR showed a 2:1 mixture of the keto:enol forms.
MS (ES) (M+H)+: 195 for C9H10N2O3
NMR: 1.13-1.29 (t, 3H), 4.05-4.28 (q, 2H), 4.18 (s, 2H), 7.62-7.76 (t, 1H), 8.95-9.06 (d, 2H), 11.79 (s, 4H).
NaH (7.84 g, 196 mmol of a 60% dispersion in oil) was added portionwise to a solution of 6.18 g (34.5 mmol) of 1-(1-methyl-1H-1,2,4-triazol-5-yl)ethanone (Ohta, S.; Kawasaki, I.; Fukuno, A.; Yamashita, M.; Tada, T.; Kawabata, T. Chem. Pharm. Bull. (1993), 41(7), 1226-31) in 100 ml dimethylcarbonate. The mixture was heated to 90° C. for 2 hour forming a thick slurry. After cooling to room temperature, the mixture was slowly transferred to 1N HCl over ice. The pH of the mixture was brought to about 7 with NaHCO3 before being saturated with NaCl and extracted 4 times with EtOAc. The EtOAc was dried (MgSO4) and concentrated to give an oil that was chromatographed on silica gel (100% DCM followed by gradient elution to 50% EtOAc in DCM). The product (5.3 g) was obtained as an oil.
NMR: 3.78 (s, 3H), 4.11 (s, 2H), 4.22 (s, 3H), 7.94 (s, 1H).
Methyl 6-(3-ethylureido)-4-(4-(trifluoromethyl)thiazol-2-yl)-3,4′-bipyridine-2′-carboxylate (Intermediate 38, 90 mg, 0.20 mmol) was dissolved in THF (2 mL) and methanol (2 mL). 1N LiOH (0.219 mL, 0.22 mmol) was added in a single portion, and the reaction mixture was heated to reflux for 15 min. The reaction mixture was cooled to room temperature and acidified with 2N HCl. The solid that precipitated was collected by filtration, washed with water and then dried in vacuo. Isolation gave 60 mg of the title compound.
LC/MS (ES+)[(M+H)+]: 438 for C18H14F3N5O3S.
1H NMR (300 MHz, d6-DMSO): 1.09 (t, 3H), 3.19 (m, 2H), 7.53 (t, 1H), 7.56 (d, 1H), 7.86 (s, 1H), 8.14 (s, 1H), 8.37 (s, 1H), 8.59 (s, 1H), 8.68 (d, 1H), 9.53 (s, 1H).
Methyl 5-bromo-2-(3-ethylureido)isonicotinate (Intermediate 6, 1 g, 3.31 mmol) was suspended in THF (5 mL) and methanol (5 mL). 1N LiOH (5 mL, 5.00 mmol) was added in a single portion, and the reaction was heated to reflux. The reaction mixture was cooled to room temperature and acidified with 2N HCl. The product precipitated from solution with the addition of water. The solid was collected by filtration and washed with water and dried in vacuo to give 843 mg of the title compound.
LC/MS (ES+[(M+H)+]: 288, 290 for C9H10BrN3O3.
1H NMR (300 MHz, d6-DMSO): 1.07 (t, 3H), 3.16 (m, 2H), 7.28 (t, 1H), 7.92 (s, 1H), 8.42 (s, 1H), 9.38 (s, 1H), 14.02 (broad s, 1H).
5-Bromo-2-(3-ethylureido)isonicotinic acid (Intermediate 51, 500 mg, 1.74 mmol) and HATU (792 mg, 2.08 mmol) were dissolved in DMF (5 mL) and DIEA (0.905 mL, 5.21 mmol). The solution was stirred for 5 min. Isonicotinohydrazide (238 mg, 1.74 mmol) was added in a single portion. The reaction mixture was diluted with water and acidified to pH 2 with 2N HCl. The solid that formed was collected by filtration, washed with water and dried in vacuo. Isolation gave 538 mg of the title compound.
LC/MS (ES+)[(M+H)+]: 407, 409 for C15H15BrN6O3.
1H NMR (300 MHz, d6-DMSO): 1.09 (t, 3H), 3.15 (m, 2H), 3.32 (d, 1H), 7.32 (m, 1H), 7.82 (m, 2H), 7.85 (s, 1H), 8.42 (s, 1H), 8.79 (m, 2H), 9.43 (s, 1H), 10.75-11.01 (d, 1H).
1-(5-Bromo-4-(2-isonicotinoylhydrazinecarbonyl)pyridin-2-yl)-3-ethylurea (Intermediate 52, 538 mg, 1.32 mmol) and triphenyl phosphine (693 mg, 2.64 mmol) were dissolved in methylene chloride (6 mL). Triethylamine (0.369 mL, 2.64 mmol) and carbon tetrabromide (876 mg, 2.64 mmol) were added sequentially. The solution was stirred at room temperature for 12 h, then diluted with water and stirred vigorously for 30 min. The organic and aqueous layers were separated and the organic layer was dried over Na2SO4, filtered and concentrated under reduced pressure. The concentrate was dissolved in minimal DMSO and purified by Gilson HPLC. Isolation gave 105 mg of the title compound.
LC/MS (ES+)[(M+H)+]: 389, 390 for C15H13BrN6O2.
In a microwave reaction vessel, 1-(5-bromo-4-(5-(pyridin-4-yl)-1,3,4-oxadiazol-2-yl)pyridin-2-yl)-3-ethylurea (Intermediate 53, 105 mg, 0.27 mmol), ethyl 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)nicotinate (82 mg, 0.30 mmol) and cesium carbonate (34.3 mg, 0.32 mmol) were combined and suspended in a 4:1 mixture of dioxane and water. Pd(PPh3)4 (15.59 mg, 0.01 mmol) was added in a single portion. The vessel was sealed, degassed, purged with nitrogen and heated to 100° C. in the microwave for 60 min. The crude reaction mixture was concentrated to dryness. The resulting residue was dissolved in DMSO, filtered and then purified by Gilson HPLC (15-55% ACN/0.1% TFA water in 14 minutes). Isolation gave 58 mg of the title compound.
LC/MS (ES+)[(M+H)+]: 460 for C23H21N7O4.
1H NMR (300 MHz, d6-DMSO): 1.05 (t, 3H), 1.23 (t, 3H), 3.16 (m, 2H), 4.29 (q, 2H), 7.38 (m, 1H), 7.63 (d, 2H), 8.30 (t, 1H), 8.37 (s, 1H), 8.45 (s, 1H), 8.76 (d, 2H), 8.83 (d, 1H), 9.08 (d, 1H), 9.53 (s, 1H).
To a solution of methyl-2-chloro-5-iodonicotinate (1.0 g, 3.37 mmol) and butanol (0.74 g, 10 mmol) in THF (80 mL) at 0° C. was added potassium hexamethyldisilizane (20 mL, 0.5N in toluene) drop wise. Slight exotherm was observed. The mixture was stirred at −2-0° C. for 1 h before quenching with acetic acid (0.5 mL) and 6N HCl (0.3 ml). The mixture was diluted with water (80 mL), and extracted with EtOAc (2×150 mL). Combined organic extracts were dried and concentrated. The residue was purified via flash chromatography (10% EtOAc-heptane) to afford 1.2 g (˜90%) of oil as a mixture (˜1:2) of methyl and butyl esters.
MS (ESP): 244.1 (M+H+) for C11H14ClNO3, methyl ester, 286.0 (M+H+) for C14H20ClNO3
A slurry of 1-ethyl-3-(5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-4-(4-(trifluoromethyl)thiazol-2-yl)pyridin-2-yl)urea (Intermediate 12, 1.4 g, 3.18 mmol), 2-butoxy-5-iodonicotinate ester mix (Intermediate 57, 1.2 g, 3.18 mmol) and K2CO3 (1.32 g, 9.6 mmol) in 1,4-dioxane-H2O (25+9 mL) was bubbled with N2 for 30 min at rt.
Bis(triphenylphosphine)palladium dichloride (0.23 g, 0.32 mmol) was added and the resulting mixture was stirred at 70-80° C. for 1 h. The mixture was cooled to room temperature, diluted with water (50 mL), and the layers were separated. The organic layer was extracted with EtOAc (2×150 mL). Combined organic layers were dried and concentrated. The residue was purified via flash chromatography (10-70% EtOAc-heptane+1% EtOH) to afford 1.6 g (˜70%) of a mixed ester of 6-butoxy-6′-(3-ethylureido)-4′-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridine-5-carboxylate as light brown gum.
MS (ESP): 524.1 (MH+) for C23H24F3N5O4S
1H NMR (d6-DMSO): δ 0.91 (t, 3H), 1.10 (t, 3H), 1.39-1.48 (m, 2H), 1.65-1.76 (m, 2H), 3.18 (q, 2H), 3.75 (s, 3H), 4.36 (t, 2H), 7.57 (bt, 1H), 8.02 (d, 1H), 8.20 (s, 1H), 8.29 (m, 2H), 8.53 (s, 1H), 9.44 (s, 1H).
The mixed ester of 6-butoxy-6′-(3-ethylureido)-4′-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridine-5-carboxylate (Intermediate 56, ˜100 mg) was stirred in 1 N NaOH (˜0.5 mL) in THF (˜3 mL) at 50° C. until no starting materials remained by LCMS. The solvent was evaporated and the sodium salt of product was purified via a reverse-phase column with 5-70% MeOH-water. The product fractions were concentrated and neutralized with HCl (1.0N) to give 6-butoxy-6′-(3-ethylureido)-4′-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridine-5-carboxylic acid.
MS (ESP): 510.0 (M+H+) for C22H22F3N5O4S
1H NMR (d6-DMSO): δ 0.93 (t, 3H), 1.10 (t, 3H), 1.39-1.48 (m, 2H), 1.65-1.76 (m, 2H), 3.19 (q, 2H), 4.27 (t, 2H), 7.63 (d, 1H), 7.84 (t, 1H), 7.93 (d, 1H), 8.17 (s, 1H), 8.30 (s, 1H), 8.55 (d, 1H), 9.62 (s, 1H).
To a 1 L round bottom flask was charged methyl 2-amino-5-bromoisonicotinate (43.7 g, 189 mmol) and tert-butanol (360 mL). The mixture was kept at 30° C., then DMAP (1.40 g, 11.48 mmol, 6%) and di-tert-butyl dicarbonate (105 g, 481 mmol, 2.54 eq) were added. The resulting mixture was heated to 80° C. for 30 minutes, then the reaction mixture was allowed to cool to room temperature and ethanol was added. The precipitated that formed was collected by filtration and washed with ethanol. After drying under vacuum overnight (˜16 hour) at 25° C., the first crop was obtained as 67.8 g of light brown solid (90.2%).
MS (ESP): 277.1 (MH+-Boc-tBu) for C17H23BrN2O6
1H NMR (300 MHz, CDCl3): δ 1.5 (s, 18H), 4.0 (s, 32H), 7.7 (s, 1H), 8.7 (s, 1H).
A solution of methyl 2-(bis(tert-butoxycarbonyl)amino)-5-bromoisonicotinate (Intermediate 58, 67.8 g, 157.3 mmol) in 7 N ammonia in methanol (600 mL) was allowed to stir at 40-50° C. in a sealed flask for overnight. The resulting mixture was evaporated to dryness and the crude product was directly used for the next step without further purification.
MS (ESP): 339.9 (M+Na+) for C11H14BrN3O3
1H NMR (300 MHz, DMSO-d6): δ 1.47 (s, 9H), 7.82 (d, 2H), 8.07 (s, 1H), 8.41 (d, 1H), 10.2 (s, 1H).
The crude tert-butyl 5-bromo-4-carbamoylpyridin-2-ylcarbamate (Intermediate 59, 157.3 mol) was treated with Lawesson's Reagent (65 g, 157.5 mmol) and tetrahydrofuran (500 mL). The resulting mixture was heated at reflux for 1 h, then it was allowed to stir at room temperature over the weekend. The mixture was concentrated to dryness in vacuo and toluene (˜200 mL) was added. After initiating, a bright yellow solid precipitated, which was collected and washed with toluene, then dried in the vacuum oven at 50° C. for 4 hours, yielding 49 g of a bright yellow solid (94%).
MS (ESP): 354.2 (M+Na+) for C11H14BrN3O2S
1H NMR (300 MHz, CDCl3): δ 1.53 (s, 9H), 7.03 (br, 1H), 7.61 (br, 1H), 7.74 (br, 1H), 8.2 (s, 1H), 8.35 (s, 1H).
To a 2 L round bottom flask was charged tert-butyl 5-bromo-4-carbamothioylpyridin-2-ylcarbamate (Intermediate 60, 48 g, 145 mmol) in tetrahydrofuran (800 mL), then solid sodium bicarbonate (24.4 g, 290 mmol) was added followed by 1,1,1-trifluoro-3-bromoacetone (31 mL, 290 mmol). The resulting mixture (yellow suspension) was allowed to stir at room temperature overnight. The white suspension was filtered and the solid was washed with water (2.2˜2.5 L). The white solid was dried under vacuum as the 1st crop (54.4, 85% yield). The mother liquor was concentrated to remove the tetrahydrofuran, filtered and washed to give after drying, 3.5 g white solid.
MS (ESP): 386.0 (M-Boc) for C14H15BrF3N3O3S
1H NMR (300 MHz, CDCl3): δ 1.6 (s, 9H), 3.3 (br, 2H), 3.6 (d, 1H), 3.9 (d, 1H), 8.2 (s, 1H), 8.5 (s, 1H).
To a 2 L round bottom flask was charged tert-butyl 5-bromo-4-(4-hydroxy-4-(trifluoromethyl)-4,5-dihydrothiazol-2-yl)pyridin-2-ylcarbamate (Intermediate 61, 54.4 g, 123 mmol) and dimethoxyethane (800 mL). The mixture was chilled in an ice-water bath, then trifluoroacetic anhydride (68 mL, 502 mmol) and 2,6-lutidine (128 mL, 1.10 mol) were added simultaneously over 30 min. The temperature of the exothermic reaction was controlled below 6° C. The orange/yellow solution which resulted was allowed to stir in the ice-water bath for half an hour, then was warmed to room temperature for 2 h. The solution was concentrated to dryness, and the residue was triturated with methanol. The precipitated solid was collected and washed with more methanol, and dried under vacuum overnight, yielding 48.3 g of white solid as the 1st crop. The mother liquor was concentrated and triturated with methanol again, the 2nd crop was obtained as a light yellow solid (1.5 g). Totally 49.8 g of product was obtained in 95.4% yield.
MS (ESP): 368.0 (M-Boc) for C14H13BrF3N3O2S
1H NMR (300 MHz, CDCl3): δ 1.6 (s, 9H), 8.0 (s, 1H), 8.2 (br, 1H), 8.55 (s, 1H), 8.65 (s, 1H).
To a sealed tube was charged tert-butyl 5-bromo-4-(4-(trifluoromethyl)thiazol-2-yl)pyridin-2-ylcarbamate (Intermediate 62, 1.2 g) with methylamine (15 mL, 2 M in methanol). The reaction mixture was heated at 145° C. for 2 h in a microwave. The mixture was concentrated to dryness to give desired product as a white solid (quantitative yield). The crude product was used directly for Suzuki couplings without further purification
MS (ESP): 381.0 (MH+) for C11H8BrF3N4OS.
The following Intermediates were synthesized according to the procedure described for Intermediate 63 from the starting materials listed in the Table.
To a sealed tube was charged 1-(5-bromo-4-(4-(trifluoromethyl)thiazol-2-yl)pyridin-2-yl)-3-methylurea (Intermediate 63, 0.41 g, 1.07 mmol), trans dichlorobis(triphenylphosphine)palladium (II) (75 mg, 10 mmol %), 1,4-dioxane (10 mL), sodium bicarbonate (180 mg, 2.14 mmol) in water (10 mL), and then methyl 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)nicotinate (0.42 g, 1.61 mmol) was added. The resulting mixture was purged by nitrogen for 5 min then heated at 50° C. for 2 h (in a microwave). Based on LC, the reaction was incomplete and the mixture was further heated at 60° C. 1 h (in a microwave). The resulting mixture was diluted with water, extracted ethyl acetate (3×), and the combined organic layers were dried over sodium sulfate. After concentration, the crude product was purified by Analogix to give the desired product as a white solid (200 mg, 42.7%).
MS (ESP): 438.0 (MH+) for C18H14F3N5O3S
1H NMR (300 MHz, CDCl3): δ 1.90 (s, 3H), 3.94 (s, 3H), 7.80 (s, 1H), 8.26 (t, 1H), 8.31 (t, 1H), 8.36 (t, 1H), 8.65 (d, 1H), 9.12 (d, 1H)
19F NMR Spectrum (300 MHz, CD3OD) −66.05
The following Intermediates were prepared according to the procedure described for Intermediate 70 from the starting materials indicated in the Table.
A solution of potassium carbonate (4 g, 28.9 mmol) in water (250 mL) was prepared and purged by N2 for a few minutes. To a 1 L round bottom flask was charged tert-butyl 5-bromo-4-(4-(trifluoromethyl)thiazol-2-yl)pyridin-2-ylcarbamate (Intermediate 62, 6 g, 14.2 mmol), trans dichlorobis(triphenylphosphine)palladium (II) (997 mg, 10 mol %) and 1,4-dioxane (300 mL). The prepared potassium carbonate solution was added followed by methyl 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)nicotinate (5.58 g, 21.2 mmol) and the mixture further diluted with 1,4-dioxane (200 mL). The resulting brown solution was purged by N2 for a further ˜10-15 min then heated to 55° C. (reflux) for ˜10-15 min. The brown solution became black. After 1 h the reaction went to completion based on LCMS. The mixture was allowed to cool and was diluted by ethyl acetate (200 mL), then washed with brine twice. The combined aqueous layers were backwashed with ethyl acetate (400 mL), and the combined organic layers dried over sodium sulfate. After concentration, a gray solid was obtained. The crude solid was purified by a silica gel plug eluted with ethyl acetate/heptane (3:4 or 3:5). After concentration, the resulting solid was further triturated with ethanol to give 5.6 g white fluffy solid. The mother liquor was concentrated and triturated with ethanol to give a 2nd crop as a white solid (0.33 g). Totally 5.93 g of product was obtained (87.2%).
MS (ESP): 481.2 (MH+) for C21H19F3N4O4S
1H NMR (300 MHz, CDCl3): δ 1.60 (s, 9H), 3.9 (s, 3H), 7.6 (s, 1H), 7.8 (d, 1H), 8.30 (t, 1H), 8.35 (s, 1H), 8.5 (s, 1H), 8.6 (d, 1H), 9.2 (d, 1H).
To a 250 mL round bottom flask was charged methyl 6′-(tert-butoxycarbonylamino)-4′-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridine-5-carboxylate (Intermediate 77, 1.6 g, 3.33 mmol) with 4 M HCl in 1,4-dioxane (110 mL), and the resulting clear solution was stirred at room temperature over the weekend (two days). Saturated sodium bicarbonate was added to the suspension was to neutralize the acid. The resulting clear solution was extracted with ethyl acetate (3×), and the combined organic layers were dried over sodium sulfate. After concentration and drying, a yellow fluffy solid was obtained in quantitative yield which was used without purification.
MS (ESP): 381.0 (MH+ average) for C11H8BrF3N4OS
To a sealed tube was charged methyl 6′-amino-4′-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridine-5-carboxylate (Intermediate 78, 330 mg, 0.87 mmol) with chloroform (5 mL), then isopropyl isocyanate (0.5 mL) was added. The resulting mixture was heated at 50° C. (oil bath) for 24 hours. The reaction was incomplete. More isopropyl isocyanate (1 mL) was added and the mixture heated at 50° C. (oil bath) for another 3 days. The resulting suspension was concentrated to dryness and triturated by ethanol. After filtration and drying, a white solid was obtained (300 mg, 74.3%).
MS (ESP): 466.2 (MH+) for C20H18F3N5O3S
1H NMR (300 MHz, CD3OD): δ 1.24 (d, 6H), 3.93-4.02 (m, 1H), 3.93 (s, 3H), 7.88 (s, 1H), 8.24 (s, 1H), 8.30 (t, 1H), 8.35 (s, 1H), 8.64 (d, 1H), 9.11 (d, 1H)
19F NMR (300 MHz, CD3OD) −66.00
To a sealed tube was charged methyl 6′-amino-4′-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridine-5-carboxylate (Intermediate 78, 350 mg, 0.921 mmol) with chloroform (5 mL), then propyl isocyanate (1.75 mL) was added. The resulting mixture was heated at 50° C. (oil bath) for 4 days. The resulting suspension was concentrated to dryness and triturated by methanol. After filtration and drying, a white solid was obtained (257 mg, 60%).
MS (ESP): 466.2 (MH+) for C20H18F3N5O3S
1H NMR (300 MHz, CD3OD): δ 0.99 (t, 3H), 1.58-1.66 (m, 2H), 3.29 (t, 2H), 3.94 (s, 3H), 7.84 (s, 1H), 8.24 (s, 1H), 8.30 (t, 1H), 8.35 (s, 1H), 8.64 (d, 1H), 9.11 (d, 1H)
19F NMR (300 MHz, CD3OD) −66.00
A suspension of 5-bromo-2-(3-ethylureido)pyridine-4-carbothioamide (Intermediates, 5.0 g, 16.5 mmol), ethyl 2-chloro-3-keto-4,4,4-trifluorobutyrate (25 g, 114 mmol) in acetonitrile (250 mL) was heated at 60° C. for 6 days. The solution was cooled triethylamine (12 mL, 87 mmol) was added followed by the dropwise addition of methane sulfonyl chloride (3.0 mL, 39 mmol). This mixture was then stirred at room temperature overnight. The solid was filtered, washed with water (500 mL) and dried in the vacuum oven at 50° C. for 12 hours to give 3.2 g (41%) of ethyl 2-(5-bromo-2-(3-ethylureido)pyridin-4-yl)-4-(trifluoromethyl)thiazole-5-carboxylate as a pale yellow solid.
MS (ESP): 467.1 and 468.9 (M+H+) for C15H14BrF3N4O3S
1H NMR (300 MHz, DMSO-d6): δ 1.08 (t, 3H), 1.34 (t, 3H), 3.17 (m, 2H), 4.40 (q, 2H), 7.20 (t, 1H), 8.54 (s, 1H), 8.59 (s, 1H), 9.43 (bs, 1H)
To a suspension of ethyl 2-(5-bromo-2-(3-ethylureido)pyridin-4-yl)-4-(trifluoromethyl)thiazole-5-carboxylate (Intermediate 81, 4.7 g, 10 mmol) in tetrahydrofuran (85 mL), was added lithium borohydride powder (653 mg, 30 mmol). The reaction was stirred for 3 hours at room temperature during which time the solution turned yellow and homogeneous. Water (50 mL) was then carefully added to the reaction and the organics were removed in vacuo. The remaining aqueous phase was extracted with ethyl acetate (3×, 50 mL). The organic extracts were combined, dried over sodium sulfate, and the solvent was removed in vacuo. This gave 4.2 g (92%) of 1-(5-bromo-4-(5-(hydroxymethyl)-4-(trifluoromethyl)thiazol-2-yl)pyridin-2-yl)-3-ethylurea as a pale yellow solid.
MS (ESP): 424.8 and 426.9 (M+H+) for C13H12BrF3N4O2S
1H NMR (300 MHz, DMSO-d6): δ 1.08 (t, 3H), 3.17 (m, 2H), 4.93 (m, 2H), 6.37 (bt, 1H), 7.26 (bt, 1H), 8.38 (s, 1H), 8.54 (s, 1H), 9.38 (bs, 1H).
The following Intermediates were synthesized by the general procedure described below from the starting material indicated in the Table.
Ethyl 2-(5-bromo-2-(3-ethylureido)pyridin-4-yl)-4-(trifluoromethyl)thiazole-5-carboxylate (Intermediate 81, 0.5 g) and excess amine (neat or 4-6 eq in ethanol solution) was heated to 80-90° C. in microwave for 3 h. The solid that formed were collected by filtration and washed by methyl tert-butyl ether to give the desired product as pale yellow or off-white solid.
The following Intermediates were synthesized by the general procedure described below from the starting material indicated in the Table.
Ethyl 2-(5-bromo-2-(3-ethylureido)pyridin-4-yl)-4-(trifluoromethyl)thiazole-5-carboxylate (Intermediate 81, 0.5 g), magnesium chloride (1 eq) and excess amine (4-6 eq in ethanol solution) was heated to 90° C. in microwave for 3 h. The solid was filtered, washed by water and methyl tert-butyl ether, then dried in vacuum oven at 50° C. for 12 hrs to give desired product as pale yellow or off-white solid.
The following Intermediates were synthesized by the general procedure described below from the starting material indicated in the Table.
1-(5-Bromo-4-(5-(hydroxymethyl)-4-(trifluoromethyl)thiazol-2-yl)pyridin-2-yl)-3-ethylurea (Intermediate 82, 0.5 g, 1.17 mmol) was dissolved in tetrahydrofuran (15 mL). Triethylamine (448 μl, 3.5 mmol) and methane sulfonyl chloride (137 μl, 1.77 mmol) were added sequentially and the reaction was stirred for 2 hours. The appropriate amine (5.9 mmol) was added, and the reaction stirred for an additional 18 hours at room temperature. The solvent was then removed in vacuo and saturated sodium bicarbonate (3 mL) was added. The suspension was extracted with ethyl acetate (3×, 3 mL) and the organic phases were combined, dried over sodium sulfate, and the solvent was removed in vacuo. The products were used without further purification.
1-(5-bromo-4-(5-((2-methoxyethylamino)methyl)-4-(trifluoromethyl)thiazol-2-yl)pyridin-2-yl)-3-ethylurea (Intermediate 90, ˜500 mg, 1 mmol), methyl 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)nicotinate (0.40 g, 1.5 mmol), and trans dichlorobis(triphenylphosphine)palladium (II) (70 mg, 0.1 mmol) were dissolved in 1,4-dioxane (10 mL). Sodium bicarbonate (252 mg, 3 mmol) was dissolved in water (3 mL) and added to the above mixture. The reaction was heated at 110° C. in a microwave for 30 minutes. Ethyl acetate (10 mL) was then added to the reaction and the layers were separated. The solvent was removed in vacuo and the residue was chromatographed on a 12 g Analogix column using 0-10% methanol in dichloromethane. The product containing fractions were combined to give the product ester (65% yield).
MS (ESP): 539.1 (M+H+) for C23H25F3N6O4S
1H NMR (300 MHz, DMSO-d6): δ 1.11 (t, 3H), 3.21 (m, 2H), 3.23 (s, 3H), 3.37 (m, 4H), 3.89 (s, 3H), 7.49 (t, 1H), 8.24 (1H), 8.28 (t, 1H), 8.37 (s, 1H), 8.74 (d, 1H), 9.02 (t, 1H), 9.11 (d, 1H), 9.52 (bs, 1H).
The following Intermediates were prepared as described for Intermediate 97 from the starting materials indicated in the Table.
methyl 6′-(3-ethylureido)-4′-(5-(2-methoxyethylcarbamoyl)-4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridine-5-carboxylate and 6′-(3-ethylureido)-4′-(5-(2-methoxyethylcarbamoyl)-4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridine-5-carboxylic acid
To a 35 mL microwave vial was added sequentially 2-(5-bromo-2-(3-ethylureido)pyridin-4-yl)-N-(2-methoxyethyl)-4-(trifluoromethyl)thiazole-5-carboxamide (Intermediate 83, 0.5 g, 1.0 mmol), methyl 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)nicotinate (0.40 g, 1.5 mmol), saturated sodium bicarbonate aqueous solution (3 mL), 1,4-dioxane (10 mL), and dichloro-bis(triphenylphosphino) palladium (II) (70 mg, 0.10 mmol). The mixture was then heated at 110° C. in a microwave for 30 min. Ethyl acetate (40 mL) and water (40 mL) were added. The aqueous layer was then further extracted with ethyl acetate (2×, 50 mL). The combined organics were dried over sodium sulfate, filtered and concentrated. The residue was loaded on 24 g Analogix silica gel column [Heptanes: (9/1) ethyl acetate/methanol] to give ester (Intermediate 105) as off-white powder. The aqueous layer was adjusted to pH ˜4 with dilute HCl and extracted with ethyl acetate/tetrahydrofuran (1/1) (3×, 100 mL). The combined organics were dried over sodium sulfate, filtered, and concentrated to give crude acid Intermediate 106 as yellow solid which was used without further purification.
Intermediate 104: Methyl 6′-(3-ethylureido)-4′-(5-(2-methoxyethylcarbamoyl)-4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridine-5-carboxylate
MS (ESP): 553.2 (M+H+) for C23H23F3N6O5S
1H NMR (300 MHz, DMSO-d6): δ 1.11 (t, 3H), 3.21 (m, 2H), 3.23 (s, 3H), 3.37 (m, 4H), 3.89 (s, 3H), 7.49 (t, 1H), 8.24 (1H), 8.28 (t, 1H), 8.37 (s, 1H), 8.74 (d, 1H), 9.02 (t, 1H), 9.11 (d, 1H), 9.52 (bs, 1H).
Intermediate 105: 6′-(3-ethylureido)-4′-(5-(2-methoxyethylcarbamoyl)-4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridine-5-carboxylic acid
MS (ESP): 539.1 (M+H+) for C22H21F3N6O5S
methyl 6′-(3-ethylureido)-4′-(5-(2-morpholinoethylcarbamoyl)-4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridine-5-carboxylate and 6′-(3-ethylureido)-4′-(5-(2-morpholinoethylcarbamoyl)-4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridine-5-carboxylic acid
To a 35 mL microwave vial was added sequentially 2-(5-bromo-2-(3-ethylureido)pyridin-4-yl)-N-(2-morpholinoethyl)-4-(trifluoromethyl)thiazole-5-carboxamide (Intermediate 84, 0.5 g, 0.9 mmol), methyl 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)nicotinate (0.36 g, 1.4 mmol), saturated sodium bicarbonate aqueous solution (3 mL), 1,4-dioxane (10 mL), and dichloro-bis(triphenylphosphino) palladium (II) (65 mg, 0.09 mmol). The mixture was then heated to 110° C. in a microwave for 30 min. Ethyl acetate (40 mL) and water (40 mL) were added. The aqueous layer was then further extracted with ethyl acetate (2×, 50 mL). The combined organics were dried over sodium sulfate, filtered, and concentrated to give the crude ester (Intermediate 106) which was used without further purification. The aqueous layer was adjusted to pH ˜4 with dilute HCl and extracted with ethyl acetate/tetrahydrofuran (1/1) (3×, 100 mL). The combined organics were dried over sodium sulfate, filtered, and concentrated to give crude acid Intermediate 107 as yellow solid which was also used without further purification.
Intermediate 106: Methyl 6′-(3-ethylureido)-4′-(5-(2-morpholinoethylcarbamoyl)-4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridine-5-carboxylate
MS (ESP): 608.1 (M+H+) for C26H28F3N7O5S
Intermediate 107: 6′-(3-ethylureido)-4′-(5-(2-morpholinoethylcarbamoyl)-4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridine-5-carboxylic acid
MS (ESP): 594.0 (M+H+) for C25H26F3N7O5S
methyl 6′-(3-ethylureido)-4′-(5-(2-(4-methylpiperazin-1-yl)ethylcarbamoyl)-4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridine-5-carboxylate and 6′-(3-ethylureido)-4′-(5-(2-(4-methylpiperazin-1-yl)ethylcarbamoyl)-4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridine-5-carboxylic acid
To a 35 mL microwave vial was added sequentially 2-(5-bromo-2-(3-ethylureido)pyridin-4-yl)-N-(2-(4-methylpiperazin-1-yl)ethyl)-4-(trifluoromethyl)thiazole-5-carboxamide (Intermediate 85, 0.5 g, 0.9 mmol), methyl 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)nicotinate (0.36 g, 1.4 mmol), saturated sodium bicarbonate aqueous solution (3 mL), 1,4-dioxane (10 mL), and dichloro-bis(triphenylphosphino) palladium (II) (65 mg, 0.09 mmol). The mixture was then heated to 110° C. in a microwave for 30 min. Ethyl acetate (40 mL) and water (40 mL) were added. The aqueous layer was then further extracted with ethyl acetate (2×, 50 mL). The combined organics were dried over sodium sulfate, filtered, and concentrated to give the crude ester (Intermediate 108) which was used for the next step without further purification. The aqueous layer was then adjusted to pH ˜6, 4, and 2 with dilute HCl, and extracted with ethyl acetate/tetrahydrofuran (1/1) however the product remained in the aqueous layer. The aqueous layer was then passed through a 30 g Analogix C18 column (acetonitrile/water) to remove most of the salts and give acid Intermediate 109 as yellow solid which was used without further purification.
Intermediate 108: Methyl 6′-(3-ethylureido)-4′-(5-(2-(4-methylpiperazin-1-yl)ethylcarbamoyl)-4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridine-5-carboxylate
MS (ESP): 621.3 (M+H+) for C27H31F3N8O4S
Intermediate 109: 6′-(3-ethylureido)-4′-(5-(2-(4-methylpiperazin-1-yl)ethylcarbamoyl)-4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridine-5-carboxylic acid
MS (ESP): 607.2 (M+H') for C26H29F3N8O4S
methyl 4′-(5-(cyclopropylcarbamoyl)-4-(trifluoromethyl)thiazol-2-yl)-6′-(3-ethylureido)-3,3′-bipyridine-5-carboxylate and 4′-(5-(cyclopropylcarbamoyl)-4-(trifluoromethyl)thiazol-2-yl)-6′-(3-ethylureido)-3,3′-bipyridine-5-carboxylic acid
To a 35 mL microwave vial was added sequentially 2-(5-bromo-2-(3-ethylureido)pyridin-4-yl)-N-cyclopropyl-4-(trifluoromethyl)thiazole-5-carboxamide (Intermediate 89, 0.5 g, 1.0 mmol), methyl 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)nicotinate (0.4 g, 1.5 mmol), saturated sodium bicarbonate aqueous solution (3 mL), 1,4-dioxane (10 mL), and dichloro-bis(triphenylphosphino) palladium (II) (70 mg, 0.1 mmol). The mixture was then heated to 110° C. in a microwave for 30 min. Ethyl acetate (40 mL) and water (40 mL) were added. The aqueous layer was then further extracted with ethyl acetate (2×, 50 mL). The combined organics were dried over sodium sulfate, filtered, and concentrated to give the crude ester (Intermediate 110) which was used without further purification. The aqueous layer was adjusted to pH ˜4 with dilute HCl and extracted with ethyl acetate/tetrahydrofuran (1/1) (3×, 100 mL). The combined organics were dried over sodium sulfate, filtered, and concentrated to give acid Intermediate 111 as yellow solid which was also used without further purification.
Intermediate 110: Methyl 4′-(5-(cyclopropylcarbamoyl)-4-(trifluoromethyl)thiazol-2-yl)-6′-(3-ethylureido)-3,3′-bipyridine-5-carboxylate
MS (ESP): 535.2 (M+H+) for C23H21F3N6O4S
Intermediate 111: 4′-(5-(cyclopropylcarbamoyl)-4-(trifluoromethyl)thiazol-2-yl)-6′-(3-ethylureido)-3,3′-bipyridine-5-carboxylic acid
MS (ESP): 521.1 (M+H+) for C22H19F3N6O4S
methyl 4′-(5-(cyclopentylcarbamoyl)-4-trifluomethyl)thiazol-2-yl)-6′-(3-ethylureido)-3,3′-bipyridine-5-carboxylate and 4′-(5-(cyclopentylcarbamoyl)-4-(trifluoromethyl)thiazol-2-yl)-6′-(3-ethylureido)-3,3′-bipyridine-5-carboxylic acid
To a 35 mL microwave vial was added sequentially 2-(5-bromo-2-(3-ethylureido)pyridin-4-yl)-N-cyclopentyl-4-(trifluoromethyl)thiazole-5-carboxamide (Intermediate 88, 0.5 g, 1.0 mmol), methyl 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)nicotinate (0.4 g, 1.5 mmol), saturated sodium bicarbonate aqueous solution (3 mL), 1,4-dioxane (10 mL), and dichloro-bis(triphenylphosphino) palladium (II) (70 mg, 0.1 mmol). The mixture was then heated to 110° C. in a microwave for 30 min. Ethyl acetate (40 mL) and water (40 mL) were added. The aqueous layer was then further extracted with ethyl acetate (2×, 50 mL). The combined organics were dried over sodium sulfate, filtered, and concentrated to give the crude ester (Intermediate 112) which was used without further purification. The aqueous layer was adjusted to pH ˜4 with dilute HCl and extracted with ethyl acetate/tetrahydrofuran (1/1) (3×, 100 mL). The combined organics were dried over sodium sulfate, filtered, and concentrated to give crude acid Intermediate 113 as yellow solid which was also used without further purification.
Intermediate 112: Methyl 4′-(5-(cyclopentylcarbamoyl)-4-(trifluoromethyl)thiazol-2-yl)-6′-(3-ethylureido)-3,3′-bipyridine-5-carboxylate
MS (ESP): 563.1 (M+H) for C25H25F3N6O4S
Intermediate 113: 4′-(5-(cyclopentylcarbamoyl)-4-(trifluoromethyl)thiazol-2-yl)-6′-(3-ethylureido)-3,3′-bipyridine-5-carboxylic acid
MS (ESP): 549.0 (M+H') for C24H23F3N6O4S
methyl 4′-(5-(cyclohexylcarbamoyl)-4-(trifluoromethyl)thiazol-2-yl)-6′-(3-ethylureido)-3,3′-bipyridine-5-carboxylate and 4′-(5-(cyclohexylcarbamoyl)-4-(trifluoromethyl)thiazol-2-yl)-6′-(3-ethylureido)-3,3′-bipyridine-5-carboxylic acid
To a 35 mL microwave vial was added sequentially 2-(5-bromo-2-(3-ethylureido)pyridin-4-yl)-N-cyclohexyl-4-(trifluoromethyl)thiazole-5-carboxamide (Intermediate 87, 0.5 g, 1.0 mmol), methyl 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)nicotinate (0.4 g, 1.5 mmol), saturated sodium bicarbonate aqueous solution (3 mL) 1,4-dioxane (10 mL), and dichloro-bis(triphenylphosphino) palladium (II) (70 mg, 0.1 mmol). The mixture was then heated to 110° C. in a microwave for 30 min. Ethyl acetate (40 mL) and water (40 mL) were added. The aqueous layer was then further extracted with ethyl acetate (2×, 50 mL). The combined organics were dried over sodium sulfate, filtered, and concentrated to give the crude ester (Intermediate 114) which was used without any further purification. The aqueous layer was adjusted to pH ˜4 with dilute HCl and extracted with ethyl acetate/tetrahydrofuran (1/1) (3×, 100 mL). The combined organics were dried over sodium sulfate, filtered, and concentrated to give crude acid Intermediate 115 as yellow solid which was also used without further purification.
Intermediate 114: Methyl 4′-(5-(cyclohexylcarbamoyl)-4-(trifluoromethyl)thiazol-2-yl)-6′-(3-ethylureido)-3,3′-bipyridine-5-carboxylate
MS (ESP): 577.1 (M+H) for C26H27F3N6O4S
Intermediate 115: 4′-(5-(cyclohexylcarbamoyl)-4-(trifluoromethyl)thiazol-2-yl)-6′-(3-ethylureido)-3,3′-bipyridine-5-carboxylic acid
MS (ESP): 563.1 (M+H+) for C25H25F3N6O4S
6-Hydroxy-nicotinic acid (100 g, 719 mmol) was suspended in methanol (1 L). 18M Sulfuric acid (50 mL) was added and the reaction was heated at reflux for 16 h. The reaction mixture was then cooled, and sodium bicarbonate powder (45 g) was added slowly to neutralize some of the acid. Most of the methanol was then removed in vacuo. Water (1 L) was added, and the pH adjusted to 7 with the careful addition of bicarbonate solution. The suspension was extracted with dichloromethane (4×, 200 mL), and the organic phases were combined, dried over sodium sulfate, and the solvent was removed in vacuo. The solid was dried in a vacuum oven at 50° C. for 1.5 h to give 83 g (75%) of methyl 6-hydroxynicotinate as a white solid.
MS (ESP): 154.2 (MH+) for C7H7NO3
1H NMR (300 MHz, CDCl3): 3.88 (s, 3H), 6.59 (dd, 1H), 8.02 (dd, 1H), 8.21 (m, 1H), 13.19 (bs, 1H).
Methyl 6-hydroxynicotininate (Intermediate 116, 50 g, 327 mmol) was suspended in acetic acid (250 mL) and bromine (26.2 mL, 490.5 mmol) was added dropwise to the reaction. The reaction was then heated at 60° C. for 18 h. The reaction mixture was cooled to room temperature, and saturated sodium thiosulfate solution was added to remove remaining bromine. Saturated sodium bicarbonate solution (500 mL) was added slowly, then 1N sodium hydroxide was added carefully until the pH was ˜7. The solid that precipitated were collected by filtration and dried in a vacuum oven at 50° C. for 18 h. This gave 76 g (100%) of methyl 5-bromo-6-hydroxynicotininate as an off white solid.
MS (ESP): 231.9 (MH+) for C7H6BrNO3
1H NMR (300 MHz, DMSO-d6): 3.80 (s, 3H), 8.12 (s, 1H), 8.19 (s, 1H), 12.77 (bs, 1H).
Methyl 5-bromo-6-hydroxynicotininate (Intermediate 117, 10 g, 43 mmol) was suspended in toluene (100 mL) and phosphorous pentoxide (12 g, 43 mmol) was added. Tetrabutyl ammonium bromide (20 g, 62.1 mmol) was added and the reaction was stirred at reflux for 5 h. The reaction mixture was cooled to ˜50° C. and toluene was decanted from the solution. Toluene (50 mL) was added to the viscous oil and heated to reflux for 30 min. The reaction mixture was cooled to ˜50° C. and toluene was decanted from the solution. This process was repeated twice more, and the toluene extracts were combined. The toluene was washed with saturated bicarbonate (2×, 30 mL), and the solvent was removed in vacuo. The residue was chromatographed on silica gel using 10-50% ethyl acetate in heptane to give 6.3 g (50%) of methyl 5,6-dibromonicotinate as an off white solid.
MS (ESP): 295.8 (MH+) for C7H5Br2NO2
1H NMR (300 MHz, DMSO-d6): 3.91 (s, 3H), 8.51 (s, 1H), 8.86 (s, 1H).
Methyl 5,6-dibromonicotinate (Intermediate 118, 1 g, 3.3 mmol) was dissolved in anhydrous tetrahydrofuran (15 mL) and the reaction was cooled to 0° C. [1,3-Bis(diphenylphosphino)propane]dichloronickel (II) (368 mg, 0.67 mmol) was added, and the solution was stirred for 5 min. Ethyl magnesium bromide (2.0M in tetrahydrofuran, 2.7 mL, 5.4 mmol) was then added dropwise over 30 min keeping the reaction at 0° C. When the addition was complete, the reaction was stirred at 0° C. for 1 h, then water (15 mL) and ethyl acetate (15 mL) were added. The layers were separated, and the aqueous phase was extracted with ethyl acetate (3×, 5 mL). The organic phases were dried over sodium sulfate, filtered and the solvent was removed in vacuo. The residue was chromatographed on a 24 g Analogix column using 0-15% ethyl acetate in heptane. This gave 408 mg (49%) of methyl 5-bromo-6-ethylnicotinate as a white semisolid.
MS (ESP): 243.9 (MH+) for C7H5Br2NO2
1H NMR (300 MHz, CDCl3): 1.33 (t, 1H), 3.08 (q, 2H), 3.92 (s, 3H), 8.35 (d, 1H), 9.01 (d, 1H).
To a slurry of 6-(3-ethylureido)-4-(4-trifluoromethylthiazol-2-yl)pyridin-3-ylboronic acid (Intermediate 12, 410 mg, 1.1 mmol), methyl 5-bromo-6-ethylnicotinate (Intermediate 119, 140 mg, 0.57 mmol) and trans dichlorobis(triphenylphosphine)palladium (II) (40 mg, 0.06 mmol) in 1,2-dimethoxyethane (12 mL) was added a solution of sodium bicarbonate (143 mg, 1.7 mmol) in water (3 mL). The reaction was stirred for 45 min at 125° C. in the microwave. The reaction mixture was cooled to room temperature, and ethyl acetate (20 mL) and water (10 mL) were added to help separate the layers. The water was removed, and the organic phase was washed with water (3 mL). The reaction was then concentrated and subjected to silica gel chromatography on a 12 g Analogix column using 0-100% ethyl acetate in heptane. This gave 60 mg (21%) of methyl 2-ethyl-6′-(3-ethylureido)-4′-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridine-5-carboxylate as an of white solid.
MS (ESP): 480.0 (MH+) for C21H20F3N5O3S
1H NMR (300 MHz, DMSO-d6): 0.98 (t, 3H), 1.11 (t, 3H), 2.39-2.51 (m, 2H), 3.18-3.28 (m, 2H), 3.92 (s, 3H), 7.61 (bt, 1H), 8.07 (d, 1H), 8.24 (s, 1H), 8.37 (s, 1H), 8.45 (s, 1H), 9.09 (d, 1H), 9.42 (bs, 1H).
The following compound was prepared according to the procedure for Intermediate 120 from the starting materials indicated in the Table.
The following Intermediates were prepared by the general procedure as described below from the starting materials indicated in the Table.
An ethyl ester (0.1 mmol) was suspended in 1:1 methanol:tetrahydrofuran (6 mL) and 1N sodium hydroxide (3 mL) was added. The reaction was stirred at room temperature for 16 h then concentrated under reduced pressure to remove the organic solvents to get a thin slurry. This slurry was acidified to pH ˜3 with 1N hydrochloric acid. This suspension was filtered and washed with water (3 mL) and dichloromethane (3 mL). The solid (or paste) was dried in a vacuum oven to give the product acid.
To a sealed tube was charge 2,6-dichloro-4-aminopyridine (5 g, 30.7 mmol), and sodium ethoxide (21 wt %, 9.92 g) with anhydrous ethanol (3 mL). The mixture was heated at 145° C. for 2 h in a microwave. Water was added, the crude product was extracted with ethyl acetate (3×), and the combined organic layers were dried over sodium sulfate, filtered and concentrated. During concentration, a crystalline solid precipitated from the crude to give clean product (2.4 g, 45.4%). The filtrate was purified (chromatography heptane/ethyl acetate) and more product (1.5 g, 25.6%) was obtained.
MS (ESP): 173.1 (MH+) for C7H9ClN2O
1H NMR (300 MHz, CD3OD): δ 1.3 (t, 3H), 4.6 (q, 2H), 5.8 (d, 1H), 6.2 (d, 1H).
To a 2 L Parr Bomb was charged 2-chloro-6-ethoxypyridin-4-amine (Intermediate 124, 3.7 g, 21.4 mmol) and methanol (300 mL). [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium (II) complex with dichloromethane (870 mg, 5 mol %) was added followed by triethylamine (6 mL) and the resulting mixture was heated at 100° C. under 100 psi CO atmosphere for 2 d. The reaction mixture was cooled to room temperature and the mixture was concentrated to dryness and directly purified by Analogix in hexane/ethyl acetate to give a light brown solid (3.7 g, 88.7%).
MS (ESP): 197.1 (MH+) for C9H12N2O3
1H NMR (300 MHz, CD3OD): δ 1.36 (t, 3H), 3.85 (s, 3H), 4.22 (q, 2H), 6.05 (d, 1H), 7.0 (d, 1H).
To a 1 L round bottom flask was charged t-butyl nitrite (1.55 mL, 11.48 mmol) with acetonitrile (200 mL), then copper (II) chloride (640 mg, 4.58 mmol) was added, and the mixture was allowed to heat at 70° C. to give a dark green solution. Methyl 4-amino-6-ethoxypicolinate (Intermediate 125, 1.51 g, 7.64 mmol) was added and gas evolution was observed. The mixture was heated at 70° C. for 1 h. After cooling to room temperature, water was added and the mixture was extracted with ethyl acetate (3×). The combined organic layers were washed with brine, ammonium chloride solution, and dried over sodium sulfate.
After concentration, the crude product was purified by Analogix (heptane/ethyl acetate 0-30%) to give a white solid (1.45 g, 88.4%).
MS (ESP): 216.0 (MH+) for C9H10ClNO3
1H NMR (300 MHz, CD3OD): δ 1.38 (t, 3H), 4.0 (s, 3H), 4.42 (q, 2H), 7.05 (d, 1H), 7.65 (d, 1H).
To a 500 mL sealed tube was charge 2,6-dichloro-4-aminopyridine (10.9 g, 66.9 mmol) with isopropanol (300 mL) and sodium hydride (95%, 9 g, 335 mmol). The mixture was heated at 150° C. for 2 d. Water was added, the crude product was extracted with ethyl acetate (3×), and the combined organic layers were dried over sodium sulfate. After concentration under reduced pressure, the crude mixture was directly used for the carbonylation without further purification.
MS (ESP): 186.9 (MH+) for C8H11ClN2O.
To a 2 L Parr Bomb was charged 2-chloro-6-isopropoxypyridin-4-amine (Intermediate 127, 12.5 g, 66.9 mmol) with methanol (300 mL). [1,1′-Bis(diphenylphosphino)ferrocene]dichloropalladium (II) complex with dichloromethane (2.80 g, 5 mol %) was added followed by triethylamine (18.8 mL). The resulting mixture was heated at 100° C. under 100 psi CO atmosphere for overnight. The mixture was concentrated to dryness and directly purified by Analogix in hexane/ethyl acetate to give a light yellow solid (10.3 g, 74%).
MS (ESP): 211.2 (MH+) for C10H14N2O3
1H NMR (300 MHz, CD3OD): δ 1.27 (d, 6H), 3.94 (s, 3H), 5.12-5.20 (m, 1H), 6.03 (d, 1H), 7.00 (d, 1H).
To a 1 L round bottom flask was charged t-butyl nitrite (6 mL, 44 mmol) with acetonitrile (200 mL), then copper (II) chloride (2.44 g, 17.2 mmol) was added, and the mixture was allowed to heat at 70° C. for 30 min to give a dark green solution. Methyl 4-amino-6-isopropoxypicolinate (Intermediate 128, 6 g, 28.6 mmol) was added and gas evolution was observed. The mixture was heated at 70° C. for 1 h. After cooling to room temperature, water was added and the mixture extracted with ethyl acetate (3×). The combined organic layers were washed with brine, ammonium chloride solution, and dried over sodium sulfate. After concentration, the crude product was purified by Analogix (heptane/ethyl acetate 0-50%) to give a light yellow liquid (4.33 g, 66%).
MS (ESP): 230.1 (MH+) for C10H12ClNO3
1H NMR (300 MHz, CD3OD): δ 1.25 (d, 6H), 3.9 (s, 3H), 5.4 (heptat, 1H), 7.00 (d, 1H), 7.60 (d, 1H).
To a 500 mL sealed tube was charge 2,6-dichloro-4-aminopyridine (10 g, 61.3 mmol) with cyclopropylmethanol (200 mL) and sodium hydride (95%, 3.2 g, 122.9 mmol). The reaction mixture was heated at 150° C. for overnight. After cooling to room temperature, water was added, the crude product was extracted with ethyl acetate (3×), and the combined org. layers were dried over sodium sulfate. After concentration, the crude mixture was purified by Analogix (heptane/ethyl acetate 0-40%) to give a white solid (12 g, 98.4%).
MS (ESP): 199.2 (MH+) for C9H11ClN2O
1H NMR (300 MHz, CD3OD): δ ppm 0.30-0.34 (m, 2H), 0.54-0.60 (m, 2H), 1.16-1.25 (m, 1H), 3.94 (d, 2H), 5.83 (d, 1H), 6.22 (d, 1H).
To a 2 L Parr Bomb was charged 2-chloro-6-(cyclopropylmethoxy)pyridin-4-amine (Intermediate 130, 9 g, 45.3 mmol.) with methanol (300 mL). [1,1′-Bis(diphenylphosphino)ferrocene]dichloropalladium (II) complex with dichloromethane (1.5 g, 6 mol %) was added followed by triethylamine (13 mL). The resulting mixture was heated at 100° C. under 100 psi CO atmosphere for 2 d. The mixture was concentrated to dryness and directly purified by Analogix in hexane/ethyl acetate system to give a light yellow solid (8.7 g, 61.4%).
MS (ESP): 223.2 (MH+) for C11H14N2O3
1H NMR (300 MHz, CD3OD): δ 0.30-0.33 (m, 2H), 0.54-0.57 (m, 2H), 1.21-1.25 (m, 1H), 3.87 (s, 3H), 4.03 (d, 2H), 4.88 (s, 2H), 6.06 (d, 2H), 7.02 (d, 2H).
To a 1 L round bottom flask wash charged t-butyl nitrite (5.5 mL, 40.5 mmol) with acetonitrile (200 mL), then copper (II) chloride (2.26 g, 16.2 mmol) was added. The mixture was allowed to heat at 70° C. for 30 min to give a dark greenish solution. Methyl 4-amino-6-(cyclopropylmethoxy)picolinate (Intermediate 131, 6 g, 27 mmol) was added and gas evolution was observed. The mixture was heated at 70° C. for 1.5 h. After cooling to room temperature, water was added and the mixture was extracted with ethyl acetate (3×). The combined organic layers were washed with brine, ammonium chloride solution, and dried over sodium sulfate. After concentration, the crude product was purified by Analogix (heptane/ethyl acetate 0-30%) to give a light yellow liquid (4.46 g, 68.5%).
MS (ESP): 242.1 (MH+) for C11H12ClNO3
1H NMR (300 MHz, CD3OD): δ 0.34-0.39 (m, 2H), 0.54-0.62 (m, 2H), 1.22-1.33 (m, 1H), 4.21 (d, 2H), 7.04 (d, 1H), 7.65 (d, 1H).
To a 500 mL sealed tube was charge 2,6-dichloro-4-aminopyridine (10 g, 61.3 mmol) with morpholine (11 mL) and 1,4-dioxane (50 mL). After heating at 150° C. for overnight the reaction was incomplete. More morpholine (11 mL) was added and the reaction again heated at 150° C. for overnight. After cooling to room temperature, water was added and the crude product was extracted with ethyl acetate (3×). The combined organic layers were dried over sodium sulfate. After concentration, the crude mixture was purified by Analogix (heptane/ethyl acetate 0-40%) to give a white solid (11.5 g, 87.8%).
MS (ESP): 214.2 (MH+) for C9H12ClN3O
1H NMR (300 MHz, CD3OD): δ 3.30 (t, 4H), 3.68 (t, 4H), 5.8 (d, 1H), 6.0 (d, 1H).
To a 2 L Parr Bomb was charged 2-chloro-6-morpholinopyridin-4-amine (Intermediate 133, 11 g, 51.4 mmol.) with methanol (300 mL). [1,1′-Bis(diphenylphosphino)ferrocene]dichloropalladium (II) complex with dichloromethane (2.11 g, 5 mol %) was added followed by triethylamine (15 mL). The resulting mixture was heated at 100° C. under 100 psi CO atmosphere for 2 d. The mixture was filtered through a Celite pad and the filtrate was washed with water and extracted with ethyl acetate (3×). The combined organic layers were dried over sodium sulfate. After concentration, the crude mixture was purified by Analogix (tetrahydrofuran/ethyl acetate 0-40%) to give an off-white solid (8.4 g, 68.7%).
MS (ESP): 238.2 (MH+) for C11H15N3O3
1H NMR (300 MHz, CD3OD): δ 3.42 (t, 4H), 3.74 (t, 4H), 3.86 (s, 3H), 6.09 (d, 1H), 6.84 (d, 1H).
To a 1 L round bottom flask wash charged t-butyl nitrite (3.6 mL, 27 mmol) with acetonitrile (200 mL), then copper (II) chloride (1.4 g, 10.08 mmol) was added, and the reaction mixture was allowed to heat at 70° C. for 30 min to give a dark greenish solution. Methyl 4-amino-6-morpholinopicolinate (Intermediate 134, 4 g, 16.8 mmol) was added and gas evolution was observed. The mixture was heated at 70° C. for 0.5 h. After cooling to room temperature, water was added and the mixture was extracted with ethyl acetate (3×). The combined organic layers were washed with brine, ammonium chloride solution, and dried over sodium sulfate. After concentration, the crude product was purified by Analogix (heptane/ethyl acetate 0-30%) to give a yellow liquid (2.6 g, 60.2%).
MS (ESP): 257.1 (MH+) for C11H13ClN2O3
1H NMR (300 MHz, CD3OD): δ 3.6 (t, 4H), 3.8 (t, 4H), 3.9 (s, 3H), 7.05 (d, 1H), 7.4 (d, 1H).
To a 500 mL sealed tube was charge 2,6-dichloro-4-aminopyridine (10 g, 61.3 mmol) with 1-methylpiperazine (8.4 mL) and 1,4-dioxane (50 mL). After heating at 170° C. for overnight the reaction was incomplete. More 1-methylpiperazine (12.6 mL) was added and the reaction heated at 170° C. for 2 d. After cooling to room temperature, water was added and the crude product was extracted with ethyl acetate (3×). Most of the bis-(1-methylpiperazine) by-product stayed in the aqueous layer. The combined organic layers were dried over sodium sulfate and after concentration the crude was used for the carbonylation.
MS (ESP): 227.1 (MH+) for C10H15ClN.
To a 2 L Parr Bomb was charged 2-chloro-6-(4-methylpiperazin-1-yl)pyridin-4-amine (Intermediate 136, 61.3 mmol) with methanol (300 mL). [1,1′-Bis(diphenylphosphino)ferrocene]dichloropalladium (II) complex with dichloromethane (2.5 g, 5 mol %) was added followed by triethylamine (17 mL). The mixture was heated at 100° C. under 100 psi CO atmosphere overnight. The reaction mixture was triturated by dichloromethane to give a product as grey solid at 90% purity (6.5 g, 42.5% in two steps).
MS (ESP): 251.1 (MH+) for C12H18N4O2
1H NMR (300 MHz, CD3OD): δ 2.9 (s, 3H), 3.3 (t, 4H), 3.9 (s, 3H), 4.9 (t, 4H), 6.2 (d, 1H), 6.9 (d, 1H).
To a 1 L round bottom flask was charged t-butyl nitrite (2 mL, 15.3 mmol) with acetonitrile (200 mL), then copper (II) chloride (850 mg, 6.12 mmol) was added, and the mixture was allowed to heat at 70° C. for 30 min to give a dark greenish solution. Methyl 4-amino-6-(4-methylpiperazin-1-yl)picolinate (Intermediate 137, 2.55 g, 10.2 mmol) was added and gas evolution was observed. The mixture was heated at 70° C. for a further 2 h. After cooling to room temperature, the mixture was filtered through a Celite pad and the filtrate was concentrated. The crude product was purified by Analogix (heptane/ethyl acetate 0-30%) to give a white solid.
MS (ESP): 270.0 (MH+) for C12H16ClN3O2
1H NMR (300 MHz, CD3OD): δ 2.95 (s, 3H), 3.55-3.65 (m, 4H), 3.90 (s, 3H), 4.6-4.7 (m, 4H), 7.22 (d, 1H), 7.45 (d, 1H).
To a 500 mL sealed tube was charge 2,6-dichloro-4-aminopyridine (10 g, 61.3 mmol), sodium hydride (60% in mineral oil, 6.1 g, 153.37 mmol) with 1-methyl-4-hydroxypiperidine (25 g, 217 mmol). Toluene (50 mL, anhydrous) was added to aid transferring 1-methyl-4-hydroxypiperidine. Bubbling in the reaction mixture was observed on addition of the piperidine. When the gas evolution ceased, the reaction mixture was heated at 120° C. for 2 h. More sodium hydride (1.4 g, 35 mmol) was added and heating continued at 120° C. for another 1.5 h. After cooling to room temperature, water was added and the crude product was extracted with dichloromethane/isopropanol (2:1) three times. The combined organic layers were dried over sodium sulfate. After concentration, the crude was used for the carbonylation.
MS (ESP): 227.1 (MH+) for C11H16ClN3O.
To a 2 L Parr Bomb was charged 2-chloro-6-(4-methylpiperazin-1-yl)pyridin-4-amine (Intermediate 139, 61.3 mmol) with methanol (300 mL). [1,1′-Bis(diphenylphosphino)ferrocene]dichloropalladium (II) complex with dichloromethane (2.5 g, 5 mol %) was added followed by triethylamine (17 mL). The mixture was heated at 100° C. under 100 psi CO atmosphere overnight. The crude reaction was filtered through Celite and the filtrate was concentrated to dryness. The crude product was directly purified by chromatography (˜2% (2M ammonia in methanol) in dichloromethane) to give a brown solid (4.75 g, 29.2%)
MS (ESP): 266.1 (MH+) for C13H19N3O3
1H NMR (300 MHz, CD3OD): δ 1.7-1.9 (m, 2H), 2.35 (s, 3H), 2.7-2.8 (m, 2H), 3.95 (s, 3H), 5.0-5.1 (m, 1H), 6.1 (s, 1H), 7.0 (s, 1H).
To a 1 L round bottom flask was charged methyl 4-amino-6-(1-methylpiperidin-4-yloxy)picolinate (Intermediate 140, 2.75 g, 10.4 mmol) with acetonitrile (200 mL). Then t-butyl nitrite (2.1 mL, 15.6 mmol) was added at 45° C. followed by copper (II) bromide (1.16 g, 5.19 mmol), and the dark greenish mixture heated at 45° C. for 2 h. After cooling to room temperature, the mixture was filtered through a Celite pad and the filtrate concentrated under reduced pressure. The crude product was directly purified by Analogix (dichloromethane/methanol) to give a light yellow solid (1 g, 29.4%).
MS (ESP): 329.1 (MH+) for C13H17BrN2O3
1H NMR (300 MHz, CD3OD): δ 2.05-2.15 (br, 4H), 2.9 (s, 3H), 3.25-3.45 (br, 4H), 3.96 (s, 3H), 5.4-5.5 (m, 1H), 7.3 (s, 1H), 7.9 (s, 1H).
To a 500 mL sealed tube was charge 2,6-dichloro-4-aminopyridine (10.1 g, 62 mmol), sodium hydride (95%, 3.2 g, 126.8 mmol) and N,N-dimethylethanolamine (50 mL). After heating at 170° C. for overnight the reaction was incomplete. More sodium hydride (0.5 g, 19.8 mmol) was added and heating continued at 170° C. for another 1.5 h. After cooling to room temperature, water was added and the crude product was extracted with dichloromethane/isopropanol (2:1) three times. The combined organic layers were dried over sodium sulfate, filtered, concentrated under reduced pressure and the crude directly used for carbonylation.
MS (ESP): 216.0 (MH+) for C9H14ClN3O.
To a 2 L Parr Bomb was charged 2-chloro-6-(2-(dimethylamino)ethoxy)pyridin-4-amine (Intermediate 142, 62 mmol) with methanol (300 mL). [1,1′-Bis(diphenylphosphino)ferrocene]dichloropalladium (II) complex with dichloromethane (2.53 g, 5 mol %) was added followed by triethylamine (17.3 mL). The resulting mixture was heated at 100° C. under 100 psi CO atmosphere overnight. The mixture was concentrated to dryness and washed with water and brine, the mixture was extracted with dichloromethane/isopropanol (2:1) and ethanol/tetrahydrorfuran (1:1). The organic layers were combined and dried over sodium sulfate. After concentration, the crude product was purified by chromatography (˜2% (2M ammonia in methanol) in dichloromethane) to give a brown sticky solid. (8.5 g, 57%)
MS (ESP): 240.3 (MH+) for C11H17N3O3
1H NMR (300 MHz, CD3OD): δ 2.4 (s, 6H), 2.8 (t, 2H), 3.9 (s, 3H), 4.4 (t, 2H), 6.1 (s, 1H), 7.1 (s, 1H).
To a 1 L round bottom flask was charged methyl 4-amino-6-(2-(dimethylamino)ethoxy)picolinate (Intermediate 143, 1.35 g, 5.6 mmol) with acetonitrile (100 mL), then t-butyl nitrite (1.2 mL, 8.5 mmol) was added. The mixture was heated at 50° C. for ˜10 min, then copper (II) bromide (1.16 g, 5.19 mmol) was added and the mixture heated at 50° C. for a further 2 h. After cooling to room temperature, the mixture was filtered through a Celite pad and the filtrate was concentrated. The crude product was purified by Analogix (dichloromethane/methanol) to give a light yellow solid (350 mg, 20.6%).
MS (ESP): 305.1 (MH+) for C11H15BrN2O3
To a microwave sealed tube was charged methyl 4-chloro-6-ethoxypicolinate (Intermediate 126, 500 mg, 2.33 mmol) and [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium (II) complex with dichloromethane (96 mg, 0.116 mmol) with dioxane (10 mL). Sodium bicarbonate (390 mg, 4.65 mmol), water (2 mL) were added, then 6-(3-ethylureido)-4-(4-(trifluoromethyl)thiazol-2-yl)pyridin-3-ylboronic acid (Intermediate 12, 920 mg, 5.12 mmol) was added, and the mixture was purged with N2 for ˜5 min. The resulting mixture was heated to 80° C. for 0.5 h. The mixture was cooled to room temperature, diluted with water, extracted with ethyl acetate (3×) and the combined organic layers were dried over sodium sulfate. After concentration, the crude mixture was purified by Analogix (heptane/ethyl acetate 0-50%) to give a white solid (300 mg, 26%).
MS (ESP): 496.2 (MH+) for C21H20H20F3N5O4S. Intermediate 146
To a microwave sealed tube was charged methyl 4-chloro-6-ethoxypicolinate (Intermediate 126, 470 mg, 2.19 mmol), [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium (II) complex with dichloromethane (53 mg, 0.0649 mmol) and 1,4-dioxane (8 mL). Then sodium bicarbonate (374 mg, 4.45 mmol), water (2 mL) and 6-(3-ethylureido)-4-(4-phenylthiazol-2-yl)pyridin-3-ylboronic acid (Intermediate 161, 820 g, 2.23 mmol) were added and the reaction mixture purged with N2 for 10 min. The resulting mixture was heated to 80° C. for 0.5 h. The reaction mixture was cooled to room temperature, diluted with water, extracted with ethyl acetate (3×) and the combined organic layers dried over sodium sulfate. After concentration under reduced pressure, the crude mixture was purified by Analogix (heptane/ethyl acetate 0-60%) to give an off-white solid (650 mg).
MS (ESP): 504.0 (MH+) for C26H25N5O4S
To a microwave sealed tube was charged methyl 4-chloro-6-isopropoxypicolinate (Intermediate 129, 510 mg, 2.23 mmol) and tetrakis(triphenylphosphine)palladium (0) (129 mg, 0.111 mmol) with 1,4-dioxane (12 mL). Then sodium bicarbonate (390 mg, 4.65 mmol), water (3 mL) and 6-(3-ethylureido)-4-(4-(trifluoromethyl)thiazol-2-yl)pyridin-3-ylboronic acid (Intermediate 12, 821 mg, 2.28 mmol) was added and the mixture purged with N2 for 5 min. The resulting mixture was heated to 80° C. for 0.5 h. The reaction mixture was cooled to room temperature, diluted with water, and extracted with ethyl acetate (3×). The combined organic layers were dried over sodium sulfate then purified by Analogix (heptane/ethyl acetate 0-100%) to give a light brown solid (900 mg).
MS (ESP): 510.0 (MH+) for C22H22F3N5O4S
To a microwave sealed tube was charged methyl 4-chloro-6-isopropoxypicolinate (Intermediate 129, 1 g, 4.36 mmol) and tetrakis(triphenylphosphine)palladium (0) (252 mg, 0.21 mmol) with 1,4-dioxane (24 mL). Sodium bicarbonate (540 mg, 8.8 mmol), water (6 mL), and 6-(3-ethylureido)-4-(4-phenylthiazol-2-yl)pyridin-3-ylboronic acid (Intermediate 161, 1.62 g, 4.38 mmol) were added. The mixture was purged with N2 for ˜5 min then heated to 80° C. for 0.5 h. The reaction mixture was cooled to room temperature, diluted with water, and extracted with ethyl acetate (3×). The combined organic layers were dried over sodium sulfate. After concentration, the crude mixture was triturated with ethanol to give a bright yellow solid which was a mixture of the desired methyl ester and de-boronated compound (1.1 g).
MS (ESP): 518.1 (MH+) for C27H27N5O4S
To a microwave sealed tube was charged methyl 4-chloro-6-(cyclopropylmethoxy)picolinate (Intermediate 132, 435 mg, 1.81 mmol), 6-(3-ethylureido)-4-(4-(trifluoromethyl)thiazol-2-yl)pyridin-3-ylboronic acid (Intermediate 12, 650 mg, 1.81 mmol) and 1,4-dioxane (12 mL). Then sodium bicarbonate (305 mg, 2.64 mmol) and water (3 mL) were added and the mixture was purged by N2 for 5 min. Tetrakis(triphenylphosphine)palladium (0) (104 mg, 0.095 mmol) was added, and the resulting mixture was heated to 80° C. for 1 h. The reaction mixture was cooled to room temperature, diluted with water, and extracted with ethyl acetate (3×). The combined organic layers were dried over sodium sulfate. After concentration under reduced pressure, the crude mixture was triturated by ethanol to give a light brown solid (100 mg).
MS (ESP): 522.1 (MH+) for C23H22F3N5O4S
To a microwave sealed tube was charged methyl 4-chloro-6-(cyclopropylmethoxy)picolinate (Intermediate 132, 328 mg, 1.36 mmol), 6-(3-ethylureido)-4-(4-phenylthiazol-2-yl)pyridin-3-ylboronic acid (Intermediate 161, 510 mg, 1.38 mmol) and 1,4-dioxane (12 mL). Sodium bicarbonate (305 mg, 2.64 mmol) was added with water (3 mL) and the mixture was purged by N2 for ˜5 min. Tetrakis(triphenylphosphine)palladium (0) (82 mg, 0.071 mmol) was added and the resulting mixture was heated to 80° C. for 1 h. The mixture was cooled to room temperature, diluted with water and extracted with ethyl acetate (3×). The combined organic layers were dried over sodium sulfate. After concentration under reduced pressure, the crude mixture was used without purification.
MS (ESP): 530.1 (MH+) for C28H27N5O4S
To a microwave sealed tube was charged methyl 4-chloro-6-morpholinopicolinate (Intermediate 135, 357 mg, 1.39 mmol), 6-(3-ethylureido)-4-(4-(trifluoromethyl)thiazol-2-yl)pyridin-3-ylboronic acid (Intermediate 12, 500 mg, 1.39 mmol) and 1,4-dioxane (15 mL). Sodium bicarbonate (240 mg, 2.86 mmol) was added with water (3 mL), the mixture was purged by N2 for 10 min, then tetrakis(triphenylphosphine)palladium (0) (90 mg, 0.078 mmol) was added. The resulting mixture was heated to 80° C. for 1 h. The reaction mixture was cooled to room temperature, diluted with water, and extracted with ethyl acetate (3×). The combined organic layers were dried over sodium sulfate. After concentration under reduced pressure, a brown solid was obtained and triturated with ethanol (cold) to give an off-white solid (350 mg, 54%).
MS (ESP): 537.0 (MH+) for C23H23F3N6O4S
To a microwave sealed tube was charged methyl 4-chloro-6-morpholinopicolinate (Intermediate 135, 492 g, 1.91 mmol), 6-(3-ethylureido)-4-(4-phenylthiazol-2-yl)pyridin-3-ylboronic acid (Intermediate 161, 700 mg, 1.91 mmol) with 1,4-dioxane (12 mL). Sodium bicarbonate (320 mg, 3.81 mmol) was added with water (3 mL), the mixture was purged by N2 for 10 min, then tetrakis(triphenylphosphine)palladium (0) (80 mg, 0.069 mmol) was added. The resulting mixture was heated to 85° C. for 1 h. The reaction was incomplete so more 6-(3-ethylureido)-4-(4-phenylthiazol-2-yl)pyridin-3-ylboronic acid (230 mg) was added with more tetrakis(triphenylphosphine)palladium (0) (84 mg, 0.073 mmol) and the resulting mixture was heated at 85° C. for two more hours. The mixture was cooled to room temperature, diluted with water, and extracted with ethyl acetate (3×). The combined organic layers were dried over sodium sulfate. After concentration, a yellow solid (700 mg) was obtained which is the mixture of the desired methyl ester, de-boronated compound and homocoupling product
MS (ESP): 545.1 (MH+) for C28H28N6O4S
To a microwave sealed tube was charged methyl 4-bromo-6-(1-methylpiperidin-4-yloxy)picolinate (Intermediate 141, 400 mg, 1.22 mmol), 6-(3-ethylureido)-4-(4-(trifluoromethyl)thiazol-2-yl)pyridin-3-ylboronic acid (Intermediate 12, 800 mg, 2.22 mmol) and 1,4-dioxane (12 mL). Then K3PO4 solution (2 N in water, 1.4 mL), and tetrakis(triphenylphosphine)palladium (0) (140 mg, 0.121 mmol) were added and the mixture was purged by N2 for ˜10 min. The resulting mixture was heated to 90° C. for 1 h. LC showed starting bromide remained so more 6-(3-ethylureido)-4-(4-(trifluoromethyl)thiazol-2-yl)pyridin-3-ylboronic acid (200 mg) was added and the mixture was heated at 90° C. for a further 1 h. The mixture was concentrated to dryness and triturated with methyl tert-butyl ether. The filtrate was concentrated and triturated by methyl tert-butyl ether again. The second filtrate was concentrated and purified by Analogix (dichloromethane/methanol) to give a light yellow solid (250 mg, 36.3%)
MS (ESP): 565.2 (MH+) for C25H27F3N6O4S
To a microwave sealed tube was charged methyl 4-bromo-6-(2-(dimethylamino)ethoxy)picolinate (Intermediate 144, 300 mg, 0.987 mmol), 6-(3-ethylureido)-4-(4-(trifluoromethyl)thiazol-2-yl)pyridin-3-ylboronic acid (Intermediate 12, 426 mg, 1.18 mmol) with 1,4-dioxane (12 mL). Then K3PO4 solution (2 N in water, 1.2 mL) was added with tetrakis(triphenylphosphine)palladium (0) (115 mg, 0.099 mmol), and the mixture purged by N2 for 10 min. The resulting mixture was heated to 90° C. for 1 h. The reaction mixture was cooled to room temperature and some solid precipitated and was filtered to give de-boronated by-product. The filtrate was diluted with water and extracted with ethyl acetate (3×). The organic layers were combined and dried over sodium sulfate, after concentration, the crude product was triturated by dichloromethane twice to remove most of the less soluble de-boronated product. The resulting filtrate was concentrated and purified by Analogix (dichloromethane/methanol) to give a light yellow sticky solid (120 mg).
MS (ESP): 539.1 (MH+) for C23H25F3N6O4S
Intermediate 155 was synthesized according to the procedure described for Intermediate 22 from Intermediate 158 and hydrazine.
LC/MS (ES+)[(M+H)+]: 460 for C23H21N7O2S.
1H NMR (300 MHz, d6-DMSO): 1.12 (t, 3H), 3.22 (m, 2H), 4.58 (s, 2H), 7.34-7.43 (m, 3H), 7.54 (d, 1H), 7.74 (d, 3H), 7.91 (s, 1H), 8.2 (d, 2H), 8.3 (s, 1H), 8.6 (d, 1H), 9.5 (s, 1H), 10.0 (s, 1H).
Intermediate 156 was synthesized according to the procedure described for Intermediate 22 from Intermediate 159 and hydrazine.
LC/MS (ES+)[(M+H)+]: 547 for C24H22N10O2S2.
1H NMR (300 MHz, d6-DMSO): 1.11 (t, 3H), 3.21 (m, 2H), 3.93 (s, 3H), 4.75 (d, 2H), 7.37 (m, 3H), 7.56 (m, 1H), 7.83 (d, 2H), 8.11 (s, 1H), 8.24 (s, 1H), 8.36 (s, 1H), 8.79 (s, 1H), 9.67 (s, 1H), 11.84 (s, 1H).
Intermediate 157 was synthesized according to the procedure described for Intermediate 22 from Intermediate 160 and hydrazine.
LC/MS (ES+)[(M+H)+]: 544 for C25H21N9O2S2.
The following intermediates were prepared in accordance to the procedure described for Intermediate 20 using the starting materials indicated in the table.
A solution of 1-(5-bromo-4-(4-phenylthiazol-2-yl)pyridin-2-yl)-3-ethylurea (2.97 g, 7.36 mmol, Intermediate 16) in THF (25 mL) was cooled to −78° C. Isopropylmagnesium chloride, 2.0M in THF (8.84 mL, 17.67 mmol) was added slowly and the reaction was slowly warmed to −15° C. before being cooled back down to −78° C. N-Butyllithium, 2.5M in hexanes (14.73 mL, 36.82 mmol) was then added and the reaction was stirred at −78° C. for 1 h. Trimethyl borate (8.21 mL, 73.64 mmol) was added all at once and an exotherm was observed. Following the exotherm, the reaction mixture was allowed to warm to room temperature and stir for 3 h. The reaction mixture was then cooled to 0° C. and 20 mL of water was added slowly followed by 10 mL of 6N HCl. The reaction mixture was allowed to warm to room temperature and stir for 30 min. The reaction mixture was concentrated under reduced pressure to remove THF. The aqueous portion was diluted with 1N NaOH and diethylether. The aqueous layer was acidified with HCl and the resulting precipitate was the title compound.
MS (ESP): 369 (M+H+) for C17H17BN4O3S.
1H NMR (DMSO-d6): δ 1.1 (t, 3H), 3.2 (q, 2H), 7.4-7.5 (m, 3H), 7.8 (s, 1H), 7.9 (s, 1H), 8.1 (d, 2H), 9.3 (s, 1H).
The 6-(3-ethylureido)-4-(4-(trifluoromethyl)thiazol-2-yl)pyridin-3-ylboronic acid (Intermediate 12, 1.20 g, 3.33 mmol), methyl 5-bromo-6-fluoronicotinate (WO200224681, 0.819 g, 3.50 mmol), tris(dibenzylideneacetone)dipalladium(0) (0.305 g, 0.33 mmol), and 2-dicyclohexylphosphino-2′,4′,6′-triisopropylbiphenyl (0.477 g, 1.00 mmol) were combined and then degassed and purged with N2 twice. A solution of sodium carbonate (0.353 g, 3.33 mmol) in water (4.5 mL) was added, followed by the addition of acetonitrile (18 mL). The flask was degassed and purged with N2 again. The mixture was heated at 80° C. for 1.5 h and then stirred at RT overnight. The mixture was conc in vacuo, diluted with EtOAc and water and filtered through a fitted funnel fitted with filter paper. The layers of the filtrate were separated. The organic layer was washed three times with sat NH4Cl, once with brine, dried over Na2SO4, and conc in vacuo. Purification via silica gel chromatography (50% acetone/hexanes; then 5-10% MeOH/CH2Cl2) gave 0.351 g (22%) of the title compound.
LC/MS (ES+)(M+H)+: 470 for C19H15F4N5O3S
1H NMR (DMSO-d6): δ 9.56 (s, 1H); 8.82 (m, 1H); 8.61 (s, 1H); 8.49 (m, 1H); 8.40 (s, 1H); 8.25 (s, 1H); 7.50 (m, 1H); 3.90 (s, 3H); 3.21 (m, 2H); 1.11 (t, 3H).
The 2-(4-methylpiperazin-1-yl)ethanol (0.154 g, 1.07 mmol) in THF (0.5 mL) was cooled to 0° C. A 1.0 M solution of lithium bis(trimethylsilyl)amide in THF (1.066 mL, 1.07 mmol) was added dropwise. The mixture was stirred at 0° C. for 10 min and then stirred at RT for 15 min. This mixture was then added dropwise to a 0° C. solution of methyl 6′-(3-ethylureido)-2-fluoro-4′-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridine-5-carboxylate (Intermediate 162, 0.115 g, 0.24 mmol) in THF (1 mL). Additional THF (0.5 mL) was added. The resultant mixture was stirred at 0° C. for 10 min and then stirred at RT for 30 min. The mixture was cooled to 0° C., quenched with satd NH4Cl and conc in vacuo. The residue was diluted with EtOAc and water and the layers were separated. The organic layer was washed with satd NH4Cl, water, brine, dried over Na2SO4 and conc in vacuo. LC/MS indicated a mixture of methyl 6′-(3-ethylureido)-2-(2-(4-methylpiperazin-1-yl)ethoxy)-4′-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridine-5-carboxylate (Intermediate 163) and 2-(4-methylpiperazin-1-yl)ethyl 6′-(3-ethylureido)-2-(2-(4-methylpiperazin-1-yl)ethoxy)-4′-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridine-5-carboxylate (Intermediate 164) which was used without further purification.
Intermediate 163: LC/MS (ES+)[(M+H)+]: 594 for C26H30F3N7O4S
Intermediate 164: LC/MS (ES+)[(M+H)+]: 706 for C32H42F3N9O4S
Hydrazine hydrate (0.117 mL, 2.40 mmol) was added to 142 mg of a mixture of methyl 6′-(3-ethylureido)-2-(2-(4-methylpiperazin-1-yl)ethoxy)-4′-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridine-5-carboxylate (Intermediate 163) and 2-(4-methylpiperazin-1-yl)ethyl 6′-(3-ethylureido)-2-(2-(4-methylpiperazin-1-yl)ethoxy)-4′-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridine-5-carboxylate (Intermediate 164). The reaction mixture was heated at 82° C. overnight. After conc in vacuo, the residue was diluted with EtOAc and water and the layers were separated. The organic layer was washed three times with satd NH4Cl, once with brine, dried over Na2SO4 and conc in vacuo to give the title compound which was used without further purification.
LC/MS (ES+)[(M+H)+]: 594 for C25H30F3N9O3S.
Methyl 2-(2-(dimethylamino)ethoxy)-6′-(3-ethylureido)-4′-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridine-5-carboxylate and 2-(Dimethylamino)ethyl 2-(2-(dimethylamino)ethoxy)-6′-(3-ethylureido)-4′-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridine-5-carboxylate
Following the procedure for Intermediates 163 and Intermediate 164, 2-(dimethylamino)ethanol (0.1 mL, 1.04 mmol) and methyl 6′-(3-ethylureido)-2-fluoro-4′-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridine-5-carboxylate (Intermediate 162, 0.112 g, 0.24 mmol) were reacted to give a mixture of methyl 2-(2-(dimethylamino)ethoxy)-6′-(3-ethylureido)-4′-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridine-5-carboxylate (Intermediate 166) and 2-(dimethylamino)ethyl 2-(2-(dimethylamino)ethoxy)-6′-(3-ethylureido)-4′-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridine-5-carboxylate (Intermediate 167) which was used without further purification.
Intermediate 166: LC/MS (ES+)[(M+H)+]: 539 for C23H25F3N6O4S
Intermediate 167: LC/MS (ES+)[(M+H)+]: 596 for C26H32F3N7O4S
Following the procedure for Intermediate 165, 0.129 g of the mixture of methyl 2-(2-(dimethylamino)ethoxy)-6′-(3-ethylureido)-4′-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridine-5-carboxylate (Intermediate 166) and 2-(dimethylamino)ethyl 2-(2-(dimethylamino)ethoxy)-6′-(3-ethylureido)-4′-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridine-5-carboxylate (Intermediate 167) was reacted to give the title compound which was used without further purification.
LC/MS (ES+)[(M+H)+]: 539 for C22H25F3N8O3S.
The methyl 6′-(3-ethylureido)-2-fluoro-4′-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridine-5-carboxylate (Intermediate 162, 0.121 g, 0.26 mmol) was suspended in THF (4 mL) and cooled to 0° C. A 0.5 M solution of sodium methoxide in MeOH (2.243 mL, 1.12 mmol) was added dropwise. The mixture was stirred at 0° C. for 20 min and then warmed to RT. After quenching with satd NH4Cl, the mixture was conc in vacuo. The residue was diluted with EtOAc and water and the layers were separated. The organic layer was washed with water, brine, dried over Na2SO4 and conc in vacuo to give the title compound which was used without further purification.
LC/MS (ES+)[(M+H)+]: 482 for C20H18F3N5O4S.
Following the procedure for Intermediate 165, methyl 6′-(3-ethylureido)-2-methoxy-4′-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridine-5-carboxylate (Intermediate 169, 0.197 g, 0.41 mmol) was reacted to give the title compound which was used without further purification.
LC/MS (ES+)[(M+H)+]: 482 for C19H18F3N7O3S.
Methyl 6′-(3-ethylureido)-2-(2-morpholinoethoxy)-4′-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridine-5-carboxylate and 2-Morpholinoethyl 6′-(3-ethylureido)-2-(2-morpholinoethoxy)-4′-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridine-5-carboxylate
Following the procedure for Intermediates 163 and Intermediate 164, 2-morpholinoethanol (0.08 mL, 0.66 mmol) and methyl 6′-(3-ethylureido)-2-fluoro-4′-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridine-5-carboxylate (Intermediate 162, 0.071 g, 0.15 mmol) were reacted to give a mixture of methyl 6′-(3-ethylureido)-2-(2-morpholinoethoxy)-4′-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridine-5-carboxylate (Intermediate 171) and 2-morpholinoethyl 6′-(3-ethylureido)-2-(2-morpholinoethoxy)-4′-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridine-5-carboxylate (Intermediate 172) which was used without further purification.
Intermediate 171: LC/MS (ES+)[(M+H)+]: 581 for C25H27F3N6O5S
Intermediate 172: LC/MS (ES+)[(M+H)+]: 680 for C30H36F3N7O6S
Following the procedure for Intermediate 165, 0.087 g of the mixture of methyl 6′-(3-ethylureido)-2-(2-morpholinoethoxy)-4′-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridine-5-carboxylate (Intermediate 171) and 2-morpholinoethyl 6′-(3-ethylureido)-2-(2-morpholinoethoxy)-4′-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridine-5-carboxylate (Intermediate 172) was reacted to give the title compound which was used without further purification.
LC/MS (ES+)[(M+H+]: 581 for C24H27F3N8O4S.
The N-[5-bromo-4-(4-(pyridin-2-yl)thiazol-2-yl)pyridin-2-yl]-N′-ethylurea (Intermediate 15, 0.965 g, 2.39 mmol) was suspended in THF (20 mL) and then cooled to −78° C. A 1.8 M solution of phenyllithium in di-n-butylether (3.18 mL, 5.73 mmol) was added dropwise. After complete addition, the reaction mixture was stirred at −78° C. for 2 h. Next, a 2.5 M solution of n-BuLi in hexanes (4.77 mL, 11.93 mmol) was added dropwise. After complete addition, the reaction mixture was stirred at −78° C. for 1 h. Trimethyl borate (2.67 mL, 23.87 mmol) was then added all at once. The cold bath was removed and the thick mixture was stirred at RT for 2 h. The mixture was re-cooled to 0° C. and water (6 mL) was added carefully, followed by 6 N HCl (6 mL, 36.00 mmol). The ice bath was then removed and the mixture was stirred at RT for 1 h and then placed in the refrigerator overnight. The aq and THF layers were separated and the THF layer was discarded. The aq layer was cooled to 0° C. and aq NaOH was added until the pH was approx. 5-6. The aq layer was extracted with several portions of EtOAc. The EtOAc extracts were conc in vacuo to give a solid. The solid was then treated with aq NaOH until the pH was >9. After diluting with MTBE, the aq and MTBE layers were separated. The aq layer was washed with several additional portions of MTBE. The MTBE layers were discarded. The aq layer was then cooled to 0° C. and treated with aq HCl until the pH was approx. 5-6. The aq layer was extracted with several portions of EtOAc. The EtOAc extracts were combined and conc in vacuo to give 0.331 g (38%) of the title compound which was used without further purification.
LC/MS (ES+)[(M+H)+]: 370 for C16H16BN5O3S.
Methyl 4-bromopicolinate (1.080 g, 5.00 mmol) was dissolved in EtOH (25.00 ml). Hydrazine hydrate (2.432 ml, 50.00 mmol) was added and the mixture was heated at 85° C. for 1 h. After cooling to RT, the mixture was conc in vacuo to give the title compound which was used without further purification.
LC/MS (ES+)[(M+H)+]: 217 for C6H6BrN3O
1H NMR (DMSO-d6): δ 10.03 (s, 1H); 8.50 (d, 1H); 8.12 (d, 1H); 7.87 (dd, 1H); 4.61 (br s, 2H).
The 4-bromopicolinohydrazide (Intermediate 175 1.080 g, 5 mmol) was suspended in trimethyl orthoacetate (10 ml, 79.57 mmol). Using a pipet, 2 drops of conc HCl were added. The mixture was heated to 115° C. for 1 h and then cooled to RT. After conc in vacuo, the resultant solid was treated with additional trimethyl orthoacetate (10 ml, 79.57 mmol) and 1,8-diazabicyclo[5.4.0]undec-7-ene (1.6 mL) and heated at 110° C. for 48 h. After cooling to RT and conc in vacuo, the residue was diluted with EtOAc and washed with several portions of satd NH4Cl until the washes were colorless. The organic layer was then washed with water, brine, dried over Na2SO4 and conc in vacuo. Purification by silica gel chromatography (0-10% MeOH/CH2Cl2) gave 0.524 g (39%) of the title compound.
LC/MS (ES+)[(M+H)+]: 241 for C8H6BrN3O
1H NMR (DMSO-d6): δ 8.65 (d, 1H); 8.33 (d, 1H); 7.93 (dd, 1H); 2.62 (s, 3H).
The 6-(3-ethylureido)-4-(4-(pyridin-2-yl)thiazol-2-yl)pyridin-3-ylboronic acid (Intermediate 174, 0.166 g, 0.45 mmol), methyl 4-bromopicolinate (0.117 g, 0.54 mmol), tetrakis (triphenylphosphine)palladium (0) (0.052 g, 0.05 mmol) and potassium carbonate (0.187 g, 1.35 mmol) were placed in a microwave vessel. The vessel was degassed and purged with N2 several times. DMF (3 mL) was added and the vessel was degassed and purged with N2 again. The vessel was heated in the microwave at 95° C. for 2 h. The mixture was filtered through a fitted funnel fitted with filter paper and rinsed with several portions of CH2Cl2 and once with EtOAc. The filtrate was then conc in vacuo. Purification by silica gel chromatography (0-10% MeOH/CH2Cl2) gave 0.037 g (18%) of the title compound.
LC/MS (ES+)[(M+H)+]: 461 for C23H20N6O3S
1H NMR (DMSO-d6): δ 9.52 (s, 1H); 8.73 (d, 1H); 8.60 (m, 1H); 8.38 (s, 1H); 8.34 (s, 1H); 8.22 (s, 1H); 8.02 (s, 1H); 7.82 (m, 1H); 7.60 (m, 3H); 7.35 (m, 1H); 3.84 (s, 3H); 3.22 (m, 2H); 1.11 (t, 3H).
The methyl 6-(3-ethylureido)-4-(4-(pyridin-2-yl)thiazol-2-yl)-3,4′-bipyridine-2′-carboxylate (Intermediate 177, 56.4 mg, 0.12 mmol), EtOH (1.75 mL), and hydrazine hydrate (0.060 mL, 1.22 mmol) were combined and heated at 85° C. for 1 h. After cooling to RT, the mixture was conc in vacuo to give the title compound which was used without further purification.
LC/MS (ES+)[(M+H)+]: 461 for C22H20N8O2S
A suspension of 4-chloropyridin-2-amine (2.186 g, 17 mmol), ethyl isocyanate (2.69 mL, 34.00 mmol) and chloroform (8 mL) was heated in the microwave at 100° C. for 1 h. The resultant solution was then concentrated in vacuo to give the title compound in quantitative yield. No further purification was performed.
LC/MS (ES+): 200, 202 for C8H10ClN3O
1H NMR (DMSO-d6): δ 9.31 (s, 1H); 8.16 (d, 1H); 7.63 (m, 1H); 7.59 (m, 1H); 7.03 (m, 1H); 3.16 (m, 2H); 1.07 (t, 3H).
A solution of 1-(4-chloropyridin-2-yl)-3-ethylurea (Intermediate 179, 3.39 g, 16.98 mmol), N-bromosuccinimide (3.02 g, 16.98 mmol), acetonitrile (32 mL), and DMF (10 mL) were combined and heated at 80° C. for 2 h. Upon cooling to RT, a precipitate formed. Water was added and the solid was collected and washed with water to give 2.78 g (59%) of the title compound which was used without further purification.
LC/MS (ES+): 278, 280 for C8H9BrClN3O
1H NMR (DMSO-d6): δ 9.37 (s, 1H); 8.44 (s, 1H); 7.92 (s, 1H); 7.17 (m, 1H); 3.15 (m, 2H); 1.06 (t, 3H).
The 1-(5-bromo-4-chloropyridin-2-yl)-3-ethylurea (Intermediate 180, 0.404 g, 1.45 mmol), ethyl 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)nicotinate (0.482 g, 1.74 mmol) and cesium carbonate (0.945 g, 2.90 mmol) were added to a microwave vessel. The vessel was degassed and purged with N2. Tetrakis(triphenylphosphine)palladium (0) (0.168 g, 0.15 mmol) was added and the vessel was degassed and purged with N2. Dioxane (10 mL) and water (2.5 mL) were added and the vessel was degassed and purged with N2 three more times. The vessel was placed in the microwave and heated at 100° C. for 2 h. The organic layer was separated and conc in vacuo. After purification by silica gel chromatography (0-10% MeOH/CH2Cl2), the resultant solid was triturated with hot acetonitrile to give 0.339 g (67%) of the title compound.
LC/MS (ES+): 349, 351 for C16H17ClN4O3
1H NMR (DMSO-d6): δ 9.47 (s, 1H); 9.12 (m, 1H); 8.92 (m, 1H); 8.37 (m, 1H); 8.33 (s, 1H); 7.85 (s, 1H); 7.46 (m, 1H); 4.38 (q, 2H); 3.18 (m, 2H); 1.35 (t, 3H); 1.09 (t, 3H).
The ethyl 4′-chloro-6′-(3-ethylureido)-3,3′-bipyridine-5-carboxylate (Intermediate 181, 0.234 g, 0.67 mmol), anhydrous hydrazine (0.211 ml, 6.71 mmol) and EtOH (10 ml) were heated at 80° C. overnight. Hydrazine hydrate (0.326 ml, 6.71 mmol) was then added and the mixture was heated at 80° C. for an additional 3 h. After cooling to RT, the mixture was diluted with MeOH and concentrated in vacuo to give the title compound which was used without further purification.
LC/MS (ES+)[(M+H)+]: 335 for C14H15ClN6O2
1H NMR (DMSO-d6): δ 10.03 (s, 1H); 9.46 (s, 1H); 9.00 (m, 1H); 8.80 (m, 1H); 8.33 (s, 1H); 8.26 (s, 1H); 7.85 (s, 1H); 7.45 (m, 1H); 4.60 (br s, 2H); 3.18 (m, 2H); 1.09 (t, 3H).
Diisopropylethylamine (0.176 ml, 1.01 mmol) was added to a solution of 1-(4-chloro-5′-(hydrazinecarbonyl)-3,3′-bipyridin-6-yl)-3-ethylurea (Intermediate 182, 0.225 g, 0.67 mmol) in DMF (6 ml). 1,1′-Carbonyldiimidazole (0.163 g, 1.01 mmol) was added in one portion and the resultant mixture was stirred at RT overnight. Water was added and the mixture was concentrated in vacuo. Purification by silica gel chromatography (0-10% MeOH/CH2Cl2) gave the title compound.
LC/MS (ES+): 361, 363 for C15H13ClN6O3
1H NMR (DMSO-d6): δ 12.83 (br s, 1H); 9.48 (s, 1H); 9.01 (m, 1H); 8.85 (m, 1H); 8.34 (s, 1H); 8.25 (m, 1H); 7.86 (s, 1H); 7.46 (m, 1H); 3.21 (m, 2H); 1.09 (t, 3H).
Following the procedure for Example 107, ethyl 4′-chloro-6′-(3-ethylureido)-3,3′-bipyridine-5-carboxylate (Intermediate 181, 0.315 g, 0.90 mmol) and 4-morpholinophenylboronic acid (0.251 g, 1.21 mmol) were heated in the microwave for 1 h at 100° C. After conc in vacuo, CH2Cl2 and water were added and the layers were separated. The organic layer was concentrated in vacuo and then purified by silica gel chromatography (0-100% EtOAc/hexanes) to give 0.268 g (62%) of the title compound.
LC/MS (ES+)[(M+H)+]: 476 for C26H29N5O4
1H NMR (DMSO-d6): δ 9.36 (s, 1H); 8.94 (m, 1H); 8.50 (m, 1H); 8.26 (s, 1H); 8.00 (m, 2H); 7.48 (s, 1H); 6.98 (m, 2H); 6.88 (m, 2H); 4.31 (q, 2H); 3.71 (m, 4H); 3.21 (m, 2H); 3.11 (m, 4H); 1.29 (t, 3H); 1.10 (t, 3H).
Hydrazine hydrate (0.215 mL, 4.42 mmol) was added to a suspension of ethyl 6′-(3-ethylureido)-4′-(4-morpholinophenyl)-3,3′-bipyridine-5-carboxylate (Intermediate 184, 0.105 g, 0.22 mmol) in EtOH (3 mL). The mixture was heated at 80° C. overnight. After cooling to RT, the mixture was diluted with MeOH and concentrated in vacuo to give the title compound which was used without further purification.
LC/MS (ES+)[(M+H)+]: 462 for C24H27N7O3
1H NMR (DMSO-d6): δ 9.93 (br s, 1H); 9.34 (s, 1H); 8.81 (m, 1H); 8.29 (m, 1H); 8.23 (s, 1H); 8.03 (m, 1H); 7.96 (m, 1H); 7.48 (s, 1H); 6.98 (m, 2H); 6.88 (m, 2H); 4.55 (br s, 2H); 3.70 (m, 4H); 3.20 (m, 2H); 3.11 (m, 4H); 1.10 (t, 3H).
To a stirred suspension of 6-hydroxypyridine-3-carboxylic acid (13.0 g, 215 mmol) in water (150 mL) was added bromine (16 mL, 310 mmol) dropwise slowly at 0° C. over a period of 30 min. The reaction mixture was stirred at 0° C. for 30 min and slowly the temperature was allowed to rise to room temperature. The reaction mixture was stirred at room temperature for 4 h. The reaction mixture was treated with saturated sodium metabisulphite solution and stirred for another 30 min at room temperature. The precipitated product was collected by filtration and washed with excess water and dried to afford 35 g (70%) of 5-bromo-6-hydroxypyridine-3-carboxylic acid as an off-white solid.
1H NMR (400 MHz, DMSO-d6) δ 8.03 (s, 1H), 8.16 (s, 1H), 12.58 (br s, 1H).
Mass: m/z 218, 220 (M, M+2)
To a stirred solution of 5-bromo-6-hydroxypyridine-3-carboxylic acid (Intermediate 186, 10 g, 45.87 mmol) in methanol (100 mL) was added sulphuric acid (1 mL) and the reaction mixture was heated to reflux overnight. The solvent was concentrated under reduced pressure to get crude compound which was poured into saturated sodium bicarbonate solution. The solid that formed was collected by filtration and dried to afford 8.5 g (80%) of methyl 5-bromo-6-hydroxypyridine-3-carboxylate.
1H NMR (400 MHz, DMSO-d6) δ 3.78 (s, 3H), 8.10 (s, 1H), 8.18 (s, 1H), 12.71 (br s, 1H).
MASS (ES): m/z 234 (M+H).
To a stirred solution of methyl 5-bromo-6-hydroxypyridine-3-carboxylate (Intermediate 187, 4.0 g, 17.24 mmol) in dry tetrahydrofuran (50 mL), was added tert-butyl 4-hydroxypiperidine-1-carboxylate (3.46 g, 17.24 mmol), and triphenylphosphine (13.42 g, 51.22 mmol) at 0° C. The reaction mixture was stirred for 10 min followed by addition of diethyl azodicarboxylate (4.0 g, 22.9 mmol). The reaction mixture was maintained at room temperature and stirred for 3 h. The solvent was concentrated under reduced pressure, then water was added and the product was extracted into ethyl acetate (2×50 mL, 1×25 mL). The combined organic layers were dried over anhydrous sodium sulphate, filtered then concentrated under reduce pressure to obtain crude compound which was purified by flash column chromatography (25-30% ethyl acetate/pet ether) to afford 5.0 g (70%) of methyl 5-bromo-6-{[1-(tert-butoxycarbonyl)piperidin-4-yl]oxy}pyridine-3-carboxylate
1H NMR (400 MHz, DMSO-d6): δ 1.45 (s, 9H), 1.85 (m, 2H), 1.95 (m, 2H), 3.48 (m, 2H), 3.65 (m, 2H), 3.91 (s, 3H), 5.39 (m, 1H), 8.39 (s, 1H), 8.70 (s, 1H).
MASS (APCI): m/z 417 (M+2).
In a round bottomed flask methyl 5-bromo-6-{[1-(tert-butoxycarbonyl)piperidin-4-yl]oxy}pyridine-3-carboxylate (Intermediate 188, 300 mg, 0.72 mmol), 1-ethyl-3-{5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-4-[4-(trifluoromethyl)-1,3-thiazol-2-yl]pyridin-2-yl}urea (Intermediate 12, 351 mg, 8.31 mmol) and cesium carbonate (470 mg, 1.44 mmol) were suspended in 1,4 dioxane:water (8:2) (25 mL). This reaction mixture was purged with Argon gas for 30 min. Tetrakis(triphenylphosphine)palladium (167 mg, 0.14 mmol) was added under argon atmosphere and the reaction mixture was heated to 80-90° C. for 3 h. The reaction mixture was cooled to room temperature, filtered through celite, the filtrate was concentrated under reduced pressure to obtain a residue which was purified by flash column chromatography (20-25% ethyl acetate/pet ether) to afford 0.25 g (56.8%) of methyl 2-{[1-(tert-butoxycarbonyl)piperidin-4-yl]oxy}-6′-[(ethylcarbamoyl)amino]-4′-[4-(trifluoromethyl)-1,3-thiazol-2-yl]-3,3′-bipyridine-5-carboxylate.
1H NMR (400 MHz, DMSO-d6): δ 1.08 (t, 3H), 1.35 (s, 9H), 1.55 (d, 2H), 3.05 (m, 3H), 3.20 (m, 6H), 3.87 (s, 3H), 5.09 (m, 1H), 7.60 (br s, 1H), 8.20 (s, 1H), 8.25 (s, 1H), 8.50 (s, 1H), 8.79 (s, 1H), 9.46 (br s, 1H).
MASS (APCI): m/z 651.1 (M+H).
To a stirred solution of methyl 2-{[1-(tert-butoxycarbonyl)piperidin-4-yl]oxy}-6′-[(ethylcarbamoyl)amino]-4′-[4-(trifluoromethyl)-1,3-thiazol-2-yl]-3,3′-bipyridine-5-carboxylate (Intermediate 189, 0.5 g, 0.76 mmol) in ethanol (20 mL) was added hydrazine hydrate (2.0 mL, 40 mmol) and the resulting mixture was heated to reflux temperature for 4 h. The reaction mixture was cooled, the solvent was concentrated under reduced pressure. Diethyl ether (10 mL) was added, and the mixture was stirred for 10 min. The resulting solid was collected by filtration and dried to afford 0.4 g (80%) of tert-butyl 4-({6′-[(ethylcarbamoyl)amino]-5-(hydrazinylcarbonyl)-4′-[4-(trifluoromethyl)-1,3-thiazol-2-yl]-3,3′-bipyridin-2-yl}oxy)piperidine-1-carboxylate as solid.
MASS (APCI): m/z 651.1 (M+H).
To a stirred solution of tert-butyl 4-({6′-[(ethylcarbamoyl)amino]-5-(hydrazinylcarbonyl)-4′-[4-(trifluoromethyl)-1,3-thiazol-2-yl]-3,3′-bipyridin-2-yl}oxy)piperidine-1-carboxylate (Intermediate 190, 300 mg, 0.46 mmol) in tetrahydrofuran (15 mL), phosgene (0.34 mL in toluene, 0.67 mmol) was slowly added at 0° C. The reaction mixture was stirred at room temperature which for 3 h. The solvent was concentrated under reduced pressure and the resulting residue was purified by flash column chromatography (5-10% ethyl acetate/pet ether) to afford 0.2 g (64.9%) of tert-butyl 4-({6′-[(ethylcarbamoyl)amino]-5-(5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)-4′-[4-(trifluoromethyl)-1,3-thiazol-2-yl]-3,3′-bipyridin-2-yl}oxy)piperidine-1-carboxylate.
1H NMR (400 MHz, CDCl3): δ 1.25 (m, 6H), 1.40 (s, 9H), 3.11 (m, 2H), 3.42 (br s, 2H), 3.51 (m 2H), 3.94 (s, 3H), 5.13 (m, 1H), 7.53 (s, 1H), 7.70 (s, 1H), 8.13 (s, 1H), 8.21 (d, 1H), 8.81 (br s, 1H), 9.04 (m, 1H).
LC-MS: m/z 677.0 (M+2).
tert-Butyl 4-({6′-[(ethylcarbamoyl)amino]-5-(hydrazinylcarbonyl)-4′-[4-(trifluoromethyl)-1,3-thiazol-2-yl]-3,3′-bipyridin-2-yl}oxy)piperidine-1-carboxylate (Intermediate 190, 200 mg, 0.30 mmol) was dissolved in triethylorthoacetate (5 mL) and the reaction mixture was heated to 120° C. for 12 h. The reaction mixture was cooled to room temperature, diluted with ethyl acetate and the organics were extracted into ethyl acetate. The combined organic layers were washed with water and brine, dried over anhydrous sodium sulphate and evaporated under reduced pressure to obtain crude compound which was purified by flash column chromatography (25-35% ethyl acetate/pet ether) to afford 100 mg 48.3% tert-butyl 4-({6′-[(ethylcarbamoyl)amino]-5-(5-methyl-1,3,4-oxadiazol-2-yl)-4′-[4-(trifluoromethyl)-1,3-thiazol-2-yl]-3,3′-bipyridin-2-yl}oxy)piperidine-1-carboxylate as solid.
1H NMR (400 MHz, CDCl3): δ 0.89 (t, 3H), 1.48 (S, 9H), 2.52 (s, 3H), 3.18 (m, 2H), 3.38-3.46 (m, 4H), 5.18 (m, 1H), 7.42-7.56 (m, 7H), 8.18-8.24 (m, 2H), 8.82 (s, 1H), 9.02 (br s, 1H)
MASS (APCI): m/z 674.2 (M−H).
To a stirred solution of methyl 5-bromo-6-hydroxypyridine-3-carboxylate (Intermediate 187, 1.0 g, 4.31 mmol) in dry tetrahydrofuran (50 mL), tert-butyl 3-hydroxypropanoate (1.26 g, 8.62 mmol) and triphenylphosphine (2.25 g, 8.62 mmol) were added and stirred for 10 min. Then the reaction mixture was cooled to 0° C., diethyl azodicarboxylate (1.5 g, 8.62 mmol) was added slowly. The reaction mixture was maintained at room temperature for 4 h. After the completion of the reaction, the solvent was concentrated under reduced pressure; water was added and the product was extracted into ethyl acetate (2×50 mL, 1×25 mL). The combined organic layers were dried over anhydrous sodium sulphate and evaporated under reduced pressure to yield the crude product which was purified by flash column chromatography (5-10% ethyl acetate/pet ether) to afford 700 mg (46%) of methyl 5-bromo-6-(3-tert-butoxy-3-oxopropoxy)pyridine-3-carboxylate.
1H NMR (400 MHz, CDCl3): δ 1.41 (s, 9H), 2.78 (t, 2H), 3.87 (s, 3H), 4.27 (t, 2H), 8.26 (s, 1H), 8.31 (s, 1H).
LC MS: m/z 360.1 (M+H).
In a round bottomed flask methyl 5-bromo-6-(3-tert-butoxy-3-oxopropoxy)pyridine-3-carboxylate (Intermediate 193, 10.7 g, 1.94 mmol), 1-ethyl-3-{5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-4-[4-(trifluoromethyl)-1,3-thiazol-2-yl]pyridin-2-yl}urea (Intermediate 12, 0.94 g, 2.13 mmol) and cesium carbonate (1.26 g, 3.88 mmol), were suspended in 1,4 dioxane: water (10 mL) (1:4) The above mixture was purged with Argon gas for 30 min. Tetrakis(triphenylphosphine)palladium (0.44 g, 0.38 mM) was added under argon atmosphere and the reaction mixture was heated to 100° C. for 4 h. After the completion of the reaction, the reaction mixture was cooled to room temperature, filtered through celite, the organic solvent was concentrated under reduced pressure to get a residue which was purified by flash column chromatography (gradient up to 40% ethyl acetate in pet ether) to afford 350 mg (30%) of methyl 2-(3-tert-butoxy-3-oxopropoxy)-6′-[(ethylcarbamoyl)amino]-4′-[4-(trifluoromethyl)-1,3-thiazol-2-yl]-3,3′-bipyridine-5-carboxylate.
LC-MS: m/z 595 (M+H).
To a solution methyl 2-(3-tert-butoxy-3-oxopropoxy)-6′-[(ethylcarbamoyl)amino]-4′-[4-(trifluoromethyl)-1,3-thiazol-2-yl]-3,3′-bipyridine-5-carboxylate (Intermediate 194, 350 mg, 0.58 mmol) in dichloromethane (20 mL), trifluoroacetic acid (335 mg, 2.94 mmol) was added and the mixture was stirred for 6 h at room temperature. Volatiles were evaporated under reduced pressure to afford the crude product, which was purified by flash column chromatography (gradient up to 5% methanol in chloroform) to afford 300 mg (96%) 3-({6′-[(ethylcarbamoyl)amino]-5-(methoxycarbonyl)-4′-[4-(trifluoromethyl)-1,3-thiazol-2-yl]-3,3′-bipyridin-2-yl}oxy)propanoic acid.
1H NMR (400 MHz, DMSO-d6): δ 1.21 (t, 1H), 1.25 (m, 2H), 1.85 (s, 2H), 2.35 (s, 2H), 3.30 (m, 2H), 3.89 (s, 3H), 4.00 (t, 2H), 7.90 (s, 1H), 8.15 (d, 2H), 8.50 (s, 1H), 8.63 (s, 1H), 9.39 (s, 1H).
LC-MS: m/z 540.3 (M+H).
To a stirred solution of 3-({6′-[(ethylcarbamoyl)amino]-5-(methoxycarbonyl)-4′-[4-(trifluoromethyl)-1,3-thiazol-2-yl]-3,3′-bipyridin-2-yl}oxy)propanoic acid (Intermediate 195, 300 mg, 0.55 mmol) in ethanol (20 mL), hydrazine hydrate (1.28 g, 25.6 mmol) was added at room temperature and the resulting reaction mixture was heated to reflux for 3 h. The reaction mixture was cooled, and the solvent was concentrated under reduced pressure. Diethyl ether (10 mL) was added and the mixture was stirred for 10 min. The obtained solid was filtered and dried to afford 240 mg (80%) of 3-({6′-[(ethylcarbamoyl)amino]-5-(hydrazinylcarbonyl)-4′-[4-(trifluoromethyl)-1,3-thiazol-2-yl]-3,3′-bipyridin-2-yl}oxy)propanoic acid.
1H NMR (400 MHz, DMSO-d6): δ 1.12 (t, 3H), 2.35 (br s, 2H), 3.22 (t, 2H), 4.01 (m, 2H), 7.65 (br s, 1H), 8.10 (s, 1H), 8.20 (d, 2H), 8.50 (d, 2H), 9.40 (s, 1H), 9.50 (br s, 1H).
To a stirred solution of methyl 5-bromo-6-hydroxypyridine-3-carboxylate (Intermediate 187, 2.0 g, 8.62 mmol) in tetrahydrofuran (50 mL), was added tetrahydro-2H-pyran-4-ylmethanol (2.0 g, 17.24 mmol), triphenylphosphine (4.51 g, 17.24 mmol) stirred for 10 min. Then the reaction mixture was cooled to 0° C. Diethyl azodicarboxylate (3.0 g, 17.24 mmol) was added slowly, and the reaction mixture was maintained at room temperature for 3 h. The solvent was concentrated under reduced pressure. Water was added and the product was extracted into ethyl acetate (2×50 mL, 1×25 mL). The combined organic layers were dried over anhydrous sodium sulphate and evaporated under reduced pressure to yield the crude product which was purified by flash column chromatography (product eluted with 5-10% ethyl acetate/pet ether) to afford 2.0 g (71%) of methyl 5-bromo-6-(tetrahydro-2H-pyran-4-ylmethoxy)pyridine-3-carboxylate.
1H NMR (400 MHz, CDCl3): δ 1.51 (m, 2H), 1.78 (d, 2H), 2.10 (m, 1H), 3.45 (t, 2H), 3.91 (s, 3H), 4.28 (d, 2H), 8.39 (s, 1H), 8.71 (s, 1H).
MASS: m/z 329.8 (M+H).
In a round bottomed flask methyl 5-bromo-6-(tetrahydro-2H-pyran-4-ylmethoxy)pyridine-3-carboxylate (Intermediate 197, 1.5 g, 4.54 mmol), 1-ethyl-3-{5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-4-[4-(trifluoromethyl)-1,3-thiazol-2-yl]pyridin-2-yl}urea (Intermediate 12, 2.22 g, 5.02 mmol) and sodium bicarbonate (0.76 g, 9.04 mmol) which was dissolved in minimum amount of water (10 mL), were combined and suspended in toluene:water (1:4). The reaction mixture was purged with argon gas for 30 min. Tetrakis(triphenylphosphine) palladium (3.31 g, 0.268 mmol) was added under argon atmosphere and the reaction mixture was heated to 80-90° C. for 5 h. The reaction mixture was cooled to room temperature, filtered through celite bed; the organic solvent was concentrated under reduced pressure to yield a residue. To this residue acetonitrile was added to obtain solid which was filtered and dried to afford 1.2 g (46%) of methyl 6′-[(ethylcarbamoyl)amino]-2-(tetrahydro-2H-pyran-4-ylmethoxy)-4′-[4-(trifluoromethyl)-1,3-thiazol-2-yl]-3,3′-bipyridine-5-carboxylate.
1H NMR (400 MHz, CDCl3) δ 1.09 (m, 3H), 1.29 (t, 5H), 1.65 (m, 1H), 3.25 (t, 2H), 3.50 (m, 2H), 3.91 (dd, 2H), 3.95 (s, 3H), 7.51 (m, 2H), 7.71 (s, 2H), 7.95 (br s, 1H), 8.15 (s, 1H), 8.25 (d, 1H), 8.95 (d 1H)
LC-MS: m/z 566.5 (M+H).
To a stirred solution of methyl 6′-[(ethylcarbamoyl)amino]-2-(tetrahydro-2H-pyran-4-ylmethoxy)-4′-[4-(trifluoromethyl)-1,3-thiazol-2-yl]-3,3′-bipyridine-5-carboxylate (Intermediate 198, 1.2 g, 2.12 mmol) in ethanol (20 mL), hydrazine hydrate (4.88 g, 97.69 mmol) was added at room temperature and the resulting reaction mixture was maintained at reflux temperature for 4 h. The reaction mixture was cooled, and the solvent was concentrated under reduced pressure to yield a residue. To this residue diethyl ether (10 mL) was added and the mixture was stirred for 10 min to obtain solid which was filtered and dried to afford 0.8 g (66%) of 1-ethyl-3-{5′-(hydrazinylcarbonyl)-2′-(tetrahydro-2H-pyran-4-ylmethoxy)-4-[4-(trifluoromethyl)-1,3-thiazol-2-yl]-3,3′-bipyridin-6-yl}urea.
1H NMR (400 MHz, DMSO-d6): δ 0.91 (m, 2H), 1.15 (t, 4H), 1.55 (m, 1H), 3.20 (m, 4H), 3.75 (d, 2H), 3.95 (d, 2H), 4.50 (br s, 1H), 7.60 (br s, 1H), 8.35 (d, 1H), 7.37 (d, 1H), 8.45 (s, 1H), 8.65 (s, 1H), 9.45 (s, 1H), 9.85 (br s, 1H)
MASS (APCI): m/z 564.7 (M−H).
The following Intermediates were prepared according to the general procedure described below from the starting materials indicated in the Table.
A suspension of methyl 6′-(3-ethylureido)-2-fluoro-4′-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridine-5-carboxylate (Intermediate 162, 0.3 g, 6 mmol, 1 eq) in the appropriate alcohol (2-3 mL, ˜50 equiv) in small vial was stirred for 2 min at room temperature. Sodium hydride (0.150 g, 60 mmol) was added over 5 min and the reaction mixture was stirred for a further 5 h at room temperature. The reaction mixture was cooled with an ice bath and slowly quenched with HCl (0.1N) solution until ˜pH 7. The aqueous layer was extracted twice with ether to remove excess alcohol. The aqueous layer was concentrated in vacuo to almost dryness than loaded on Analogix C18-column for reverse phase purification (water-methanol) to remove excess of salt.
A suspension of methyl 6′-(3-ethylureido)-2-fluoro-4′-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridine-5-carboxylate (Intermediate 162, 0.3 g, 6 mmol) in dimethyl formamide (3 mL) was treated with 1,2,2,6,6-pentamethylpiperidin-4-ol (5 eq) and potassium hexamethyl disilylazide (5 equivalents) in a small vial. The reaction was stirred for 48 h at room temperature. The dimethyl formamide was removed under vacuum, and the residue cooled with an ice bath and slowly quenched with HCl (0.1N) solution until pH 7. The aqueous layer was concentrated in vacuo to almost dryness than loaded on Analogix C18-column for reverse phase purification (water-methanol) to remove remaining starting materials and give an off-white solid.
MS (ESP): 606.22 (MH+) for C28H33F3N6O4S
A suspension of methyl 6′-(3-ethylureido)-2-fluoro-4′-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridine-5-carboxylate (Intermediate 162, 0.3 g, 6 mmol, 1 eq) in 2-tert-butoxyethanol (2-3 mL) in a small vial was stirred for 2 min at room temperature. Sodium hydride (0.150 g, 60 mmol) was added over 5 min and the reaction mixture was stirred for a further 5 h at room temperature. The reaction was cooled with an ice bath and slowly quenched with HCl (0.1N) solution to pH 7. The aqueous layer was extracted twice with ether to remove excess of alcohol. The aqueous layer was concentrated in vacuo to almost dryness than loaded on Analogix C18-column for reverse phase purification (water-methanol) to remove excess salt and give an off-white solid.
MS (ESP): 553.16 (MH+) for C24H26F3N5O5S.
A suspension of 2-(2-tert-butoxyethoxy)-6′-(3-ethylureido)-4′-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridine-5-carboxylic acid (Intermediate 204, 0.3 mmol), and hydrazine acetate (0.9 mmol) in phosphorus oxychloride (2.5 mL) was heated at 70° C. for 2 h. The solution was then cooled and concentrated to dryness. A solution of saturated potassium carbonate was added to the crude and product was extracted with ethyl acetate (3×). The combined organic layers were washed with brine and dried over sodium sulfate. All solvents were removed under vacuum and the crude was purified by Analogix using dichloromethane-methanol.
MS (ESP): 553.09 (MH+) for C22H19ClF3N7O3S.
The following Intermediates were synthesized according to the general procedure described below from the starting materials indicated in the Table.
A suspension of corresponding carboxylic acid (0.3 mmol) in thionyl chloride (2 mL) was heated at 50° C. for 1 h. The solution was then cooled and concentrated under reduced pressure to dryness. The crude suspended in tetrahydrofuran (2 mL) was added slowly to a solution of hydrazine/tetrahydrofuran (1/2 vol., 3 mL) and stirred at room temperature for 12 h. The crude reaction mixture was concentrated to dryness and purified by reverse phase on Analogix C18-column (water-methanol) to give a (˜60%) hydrazide as an off-white solid.
To (S)-methyl 2-(tert-butoxycarbonylamino)-3-methylbutanoate (5 g, 0.0215 mol) in ethanol (50 mL) was added hydrazine hydrate (16 mL, 0.323 mol) and the solution heated at 70° C. overnight. The solvent was evaporated and the residue dissolved in ethyl acetate, washed with water, dried over sodium sulfate and the solvent evaporated to give ˜3 g of product.
A suspension of 2-(2-(diethylamino)ethoxy)-6′-(3-ethylureido)-4′-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridine-5-carboxylic acid (Intermediate 202, 0.3 mmol) in tetrahydrofuran (2 mL) was treated with (S)-tert-butyl 1-hydrazinyl-3-methyl-1-oxobutan-2-ylcarbamate (Intermediate 210, 0.6 mmol), O-(7-azabenzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium hexafluorophosphate (HATU, 0.4 mmol) and triethyl amine (0.6 mmol) at room temperature for 12 h. The solution was then concentrated to dryness and purified by Analogix silica gel chromatography (dichloromethane-methanol) to give (60%) of (S)-tert-butyl 1424242-(diethylamino)ethoxy)-6′-(3-ethylureido)-4′-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridine-5-carbonyl)hydrazinyl)-3-methyl-1-oxobutan-2-ylcarbamate as an off-white solid.
MS (ESP): 766 (MH+) for C34H46F3N9O6S.
A suspension of (5)-tert-butyl 1-(2-(2-(2-(diethylamino)ethoxy)-6′-(3-ethylureido)-4′-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridine-5-carbonyl)hydrazinyl)-3-methyl-1-oxobutan-2-ylcarbamate (Intermediate 211, 0.3 mmol) in tetrahydrofuran (2 mL) was treated with triphenylphosphine (0.6 mmol), and carbon tetrachloride (0.6 mmol) at room temperature for 12 h. The solution was then concentrated to dryness and purified by Analogix silica gel chromatography (dichloromethane-methanol) to give an off-white solid (80%).
MS (ESP): 748.3 (MH+) for C34H44F3N9O5S.
Methyl 2-amino-5-bromoisonicotinate (100 g, 433 mmol) was dissolved in chloroform (600 mL) and placed into a 1 L sealed tube. Propyl isocyanate (122.5 mL, 1.29 mol) was then added. The reaction was heated at 55° C. for 72 h at which time the reaction was determined to be complete. The mixture was then cooled to room temperature, concentrated under reduced pressure, and the solid was dissolved in 2:1 ethyl acetate: tetrahydrofuran (3 L). This solution was washed with water (2×, 200 mL), and the water was back extracted with ethyl acetate (300 mL). The organic layers were then dried with sodium sulfate, filtered, and concentrated yielding 129 g (95%) of methyl 5-bromo-2-(3-propylureido)isonicotinate as a dark yellow solid.
MS (ESP): 316.1 (MH+) for C11H14BrN3O3
1H NMR (300 MHz, CDCl3): δ 0.88 (t, 3H), 1.45 (m, 2H), 3.11 (m, 2H), 3.90 (s, 3H), 7.21 (bt, 1H), 8.02 (s, 1H), 8.46 (s, 1H), 9.40 (s, 1H)
A solution of methyl 5-bromo-2-(3-propylureido)isonicotinate (Intermediate 213, 128 g, 405 mmol) and 7N ammonia in methanol (1 L) was allowed to stir at room temperature for 3 d, then the solids were allowed to settle. The precipitated was vacuum filtered, rinsed with methanol (2×, 500 mL), and dried on the high vacuum pump overnight, yielding 123 g (quant) of 5-bromo-2-(3-propylureido)isonicotinamide as a white solid.
MS (ESP): 301.1 (MH+) for C10H13BrN4OS
1H NMR (300 MHz, DMSO-d6): δ 0.88 (t, 3H), 1.46 (m, 2H), 3.18 (q, 2H), 7.41 (bs, 1H), 7.58 (s, 1H), 7.78 (bs, 1H), 8.08 (bs, 1H), 8.33 (s, 1H), 9.31 (s, 1H)
A suspended mixture of 5-bromo-2-(3-propylureido)isonicotinamide (Intermediate 214, 123 g, 407 mmol), Lawesson's Reagent (131.6 g, 326 mmol), and tetrahydrofuran (1.55 L) was stirred at 70° C. for 18 h. Stirring was stopped and a bright yellow precipitate was allowed to settle. The precipitate was vacuum filtered and washed with methyl tert-butyl ether (2×, 500 L). This solid was then dried in the vacuum oven at 50° C. for 12 hours to give 50 g of product solid. The mother liquor was concentrated and the residue was suspended in toluene (300 mL). The solid thus obtained was filtered and combined with the previous solid. The combined totaled 110 g (85%) of 5-bromo-2-(3-propylureido)pyridine-4-carbothioamide as an off white solid
MS (ESP): 317.2 (MH+) for C10H13BrN4OS
1H NMR (300 MHz, CDCl3): δ 0.88 (t, 3H), 1.42 (m, 2H), 3.13 (m, 2H), 7.38 (s, 1H), 7.50 (s, 1H), 8.28 (s, 1H), 9.25 (s, 1H), 9.80 (s, 1H), 10.28 (s, 1H)
A suspension of 5-bromo-2-(3-propylureido)pyridine-4-carbothioamide (Intermediate 215, 100 g, 315 mmol), 3-bromo-1,1,1-trifluoroacetone (64 mL, 630 mmol) in acetonitrile (1.5 L) was heated at 80° C. for 20 hours. The solution was then cooled down and was concentrated under reduced pressure to give an orange oil that was carried on without further purification.
MS (ESP): 426.9 (MH+) for C13H14BrF3N4O2S
1H NMR (300 MHz, DMSO-d6): δ 0.88 (t, 3H), 1.48 (m, 2H), 3.11 (m, 2H), 3.62 (d, 1H), 3.92 (d, 1H), 7.30 (bs, 1H), 7.98 (s, 1H), 8.46 (s, 1H), 9.42 (s, 1H).
A solution of 1-(5-bromo-4-(4-hydroxy-4-(trifluoromethyl)-4,5-dihydrothiazol-2-yl)pyridin-2-yl)-3-propylurea (Intermediate 216, 315 mmol) and triethylamine (217 mL, 1.57 mol) in tetrahydrofuran (1.3 L) was prepared and stirred at room temperature. Methane sulfonyl chloride (61 mL, 787 mmol) was added dropwise over the course of 1 h. This mixture was stirred at 26° C. for 4 h. Stirring was then stopped and the solids were filtered, washed with tetrahydrofuran (3×, 200 mL), and discarded. The combined tetrahydrofuran layers were concentrated to a viscous, yellow semi-solid which was then triturated with methanol (1 L). The solid was filtered and washed with methanol (2×, 300 mL), then dried in the vacuum oven at 50° C. for 12 h to give 99.4 g (76%) of 1-(5-bromo-4-(4-(trifluoromethyl)thiazol-2-yl)pyridin-2-yl)-3-propylurea as an off-white solid.
MS (ESP): 409.1 (MH+) for C13H12BrF3N4OS
1H NMR (300 MHz, DMSO-d6): δ 0.89 (t, 3H), 1.47 (m, 2H), 3.16 (m, 2H), 7.25 (s, 1H), 8.41 (s, 1H), 8.57 (s, 1H), 8.82 (s, 1H), 9.39 (s, 1H).
A suspension of 1-(5-bromo-4-(4-(trifluoromethyl)thiazol-2-yl)pyridin-2-yl)-3-propylurea (Intermediate 217, 50 g, 123 mmol) in tetrahydrofuran (1.25 L) was prepared and stirred at −50° C. 2.0 M isopropyl magnesium chloride in tetrahydrofuran (183 mL, 368 mmol) was added dropwise over 45 min so that the temperature never rose above −35° C. The reaction mixture was stirred for a further hour at −40° C. then was cooled to −78° C. A solution of 2.5 M n-butyl lithium in hexanes (295 mL, 735 mmol) was then added dropwise to the reaction solution over the course of 1 h so that the temperature never rose above −65° C. This mixture was then allowed to react at −78° C. for 1.5 h. Boron methoxide (164 mL, 1.47 mol) was added in 1 portion and the cold bath was removed. The reaction was allowed to warm to room temperature and stir for 1 h. 3N Hydrochloric acid (500 mL) was then added slowly to minimize foaming and the reaction was stirred at room temperature for 30 min so that all of the solids dissolved. The reaction was concentrated to remove the tetrahydrofuran and water (1 L) was added. The solution was basified to pH 10 with 24% sodium hydroxide and the total volume was increased to 2 L with water. The aqueous solution was extracted with methyl tert-butyl ether (3×, 650 mL). The organic layers were combined and extracted with 5% sodium hydroxide (100 mL). The aqueous phases were combined and acidified to pH 5.5 with 6N hydrochloric acid causing a suspension to form. This suspension was extracted with 2:1 ethyl acetate: THF (5×, 400 mL) ensuring all solid dissolved in the organic phase. The organic phases were combined and back washed with water (1 L). The organics were concentrated and triturated with methyl tert-butyl ether (1 L). The solid obtained was dried in a vacuum oven at 50° C. for 18 h. This gave 25 g (55%) of 6-(3-propylureido)-4-(4-(trifluoromethyl)thiazol-2-yl)pyridin-3-ylboronic acid as an off-white solid.
MS (ESP): 375.0 (MH+) for C13H14BF3N4O3S
1H NMR (300 MHz, DMSO-d6): δ 0.90 (t, 3H), 1.45-1.52 (m, 2H), 3.07-3.16 (m, 2H), 7.81 (bt, 1H), 7.91 (s, 1H), 8.20 (br, 2H), 8.31 (d, 1H), 8.65 (m, 1H), 9.32 (s, 1H)
To a slurry of 6-(3-propylureido)-4-(4-trifluoromethylthiazol-2-yl)pyridin-3-ylboronic acid (Intermediate 218, 4.2 g, 11.1 mmol), methyl 5-bromo-6-fluoronicotinate (2.0 g, 8.5 mmol) and trans dichlorobis(triphenylphosphine)palladium (II) (597 mg, 0.85 mmol) in 1,4-dioxane (72 mL) was added a solution of potassium carbonate (2.4 g, 17.0 mmol) in water (27 mL) and the mixture was stirred at 70° C. for 1 h. The reaction was cooled to room temperature, and ethyl acetate (100 mL) and water (10 mL) were added to help separate the layers. The water was removed, and the organic phase was washed with water (10 mL). The organic layer was then concentrated and the resulting residue was triturated with a mixture of ethanol (20 mL) and methyl tert-butyl ether (50 mL). The solid was dried in a vacuum oven at 50° C. for 3 h to give 1.7 g (42% yield) of methyl 2-fluoro-6′-(3-propylureido)-4′-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridine-5-carboxylate as an off white solid.
MS (ESP): 484.2 (MH+) for C20H17F4N5O3S
1H NMR (300 MHz, DMSO-d6): δ 0.91 (t, 3H), 1.49 (m, 2H), 3.16 (m, 2H), 3.93 (s, 3H), 7.58 (bt, 1H), 8.23 (s, 1H), 8.39 (s, 1H), 8.48 (dd, 1H), 8.60 (s, 1H), 8.81 (d, 1H), 9.56 (bs, 1H).
A suspension of methyl 6′-(3-propylureido)-2-fluoro-4′-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridine-5-carboxylate (Intermediate 219, 0.3 g, 6 mmol) in diisopropylaminoethanol (2-3 mL, ˜50 equiv.) in small vial was stirred for 2 min at room temperature. Sodium hydride (0.150 g, 60 mmol) was added over 5 minutes and the reaction was stirred for a further 5 h at room temperature. The reaction mixture was cooled with an ice bath and slowly quenched with HCl (0.1N) solution until pH 7. The aqueous layer was extracted twice with ether to remove excess alcohol. The aqueous layer was concentrated in vacuo to almost dryness, then loaded on Analogix C18-column for reverse phase purification (water-methanol) to remove excess of salt.
MS (ESP): 594.22 (M+H+) for C27H33F3N6O4S.
A suspension of 2-(2-(diisopropylamino)ethoxy)-6′-(3-propylureido)-4′-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridine-5-carboxylic acid (Intermediate 220, 0.3 mmol) in thionyl chloride (2 mL) was heated at 50° C. for 1 h. The solution was then cooled and concentrated to dryness. The crude suspended in tetrahydrofuran (2 mL) was added slowly to a solution of hydrazine/tetrahydrofuran (1/2 vol., 3 mL) and stirred at room temperature for 12 h. The crude reaction mixture was concentrated under reduced pressure to dryness and purified by reverse phase on Analogix C18-column (water-methanol) to give the hydrazide as off-white solid.
MS (ESP): 609.2 (MH+) for C27H35F3N8O3S
A mixture of 1-(5-Bromopyridin-3-yl)-3-(dimethylamino)prop-2-en-1-one (Intermediate 223, 300 mg, 1.18 mmol) and hydrazine (0.111 mL, 3.53 mmol) in ethanol (3 mL) was heated to reflux for 1.5 h. The solvent was removed and the crude light yellow solid (245 mg), which was used without further purification.
MS (ESP): 226 (M+2) for C8H6BrN3
1H-NMR (DMSO-d6) δ: 6.94 (d, 1H); 7.85 (brs, 1H); 8.41 (s, 1H); 8.62 (d, 1H); 9.04 (d, 1H); 13.20 (brs, 1H)
1-(5-Bromopyridin-3-yl)ethanone (1.3 g, 6.50 mmol) and 1,1-dimethoxy-N,N-dimethylmethanamine (5 mL, 6.50 mmol) were taken in a round bottomed flask and heated at 120° C. for 1 h. The reaction mixture was cooled to room temperature and then partitioned between water and ethyl acetate. The layers were separated and the organic layer was washed with water two times, then dried over magnesium sulfate and concentrated under reduced pressure to give a bright orange colored solid (1.4 g) as the product.
MS (ESP): 257 (M+2) for C10H11BrN2O
The following compounds have been synthesized as described for Example 21 from the starting materials indicated in the table below.
The following compounds have been synthesized as described for Intermediate 9 from the starting materials indicated in the table below.
To a suspension of 5-bromo-2-(3-ethylureido)pyridine-4-carbothioamide (Intermediate 5, 25 g, 82.46 mmol) in acetonitrile (150 mL), 3-bromo-1,1,1-trifluoropropan-2-one (12.84 mL, 123.69 mmol) was added and the mixture was heated to reflux for 5 h. The reaction mixture was cooled to room temperature, filtered, and the filtrate was concentrated under reduced pressure. The resulting residue was slurried in ethylaceate, filtered, and washed with methanol. The solid obtained was taken to the next step.
MS (ESP): 429 (M+2) for C13H14BrF3N4O2S
1H-NMR (DMSO-d6) δ: 1.07 (t, 3H); 3.08-3.24 (m, 2H); 3.40 (s, 3H); 3.93 (s, 1H); 3.96 (s, 1H); 7.13 (t, 1H); 7.99 (s, 1H); 8.51 (s, 1H); 9.43 (s, 1H).
The title compound was synthesized by a method analogous to the synthesis of the Intermediate 12 starting with 1-(5-bromo-4-(5-methyl-4-(trifluoromethyl)thiazol-2-yl)pyridin-2-yl)-3-ethylurea (Intermediate 244) and 4,4,4′,4′,5,5,5′,5′-octamethyl-2,2′-bi(1,3,2-dioxaborolane).
MS (ESP): 457 (M+1) for C19H24BF3N4O3S
To a 1 M solution of potassium tert-butoxide (413 μl, 0.41 mmol) in THF, 5-(5-bromopyridin-3-yl)-1,3,4-oxadiazol-2(3H)-one (Intermediate 485 100 mg, 0.41 mmol) was added. To this mixture 2 mL of THF was added and the mixture was stirred for 30 min at room temperature. Then methyl iodide (51.7 μl, 0.83 mmol) was added and DMF (2 mL) was added as a co-solvent in order to dissolve the starting material, and the resulting suspension was stirred for an additional 30 min. Then water was added and the precipitated product was isolated by filtration. The precipitate was slurried with acetonitrile, filtered and dried to give a nice white solid (75 mg). MS (ESP): 258 (M+2) for C8H6BrN3O2
1H-NMR (DMSO-d6) δ: 3.44 (s, 3H); 8.37 (t, 1H); 8.91 (d, 1H); 8.95 (d, 1H).
The title compound was synthesized by a method analogous to the synthesis of the Intermediate 3 starting with 1-(5-bromo-4-(4-hydroxy-5-methyl-4-(trifluoromethyl)-4,5-dihydrothiazol-2-yl)pyridin-2-yl)-3-ethylurea (Intermediate 248).
MS (ESP): 411 (M+2) for C13H12BrF3N4OS
1H-NMR (DMSO-d6) δ: 1.08 (t, 3H); 2.69 (s, 3H); 3.10-3.24 (m, 2H); 7.26 (t, 1H); 8.39 (s, 1H); 8.54 (s, 1H); 9.39 (s, 1H).
The title compound was synthesized by a method analogous to the synthesis of the intermediate 4 starting with 5-bromo-2-(3-ethylureido)pyridine-4-carbothioamide (Intermediate 5) and 3-bromo-1,1,1-trifluorobutan-2-one.
MS (ESP): 429 (M+2) for C13H14BrF3N4O2S.
To a solution of 1-(4-(3,3-dimethylpiperidin-1-yl)pyridin-2-yl)-3-ethylurea (Intermediate 253, 200 mg, 0.72 mmol), in DMF (3 mL), N-bromo-succinamide (NBS, 129 mg, 0.72 mmol) was added. The resulting solution was heated at 80° C. for 1 hr. The reaction was then partitioned between water and ethyl acetate. The layers separated and the organic layer was washed with water and brine, then dried over magnesium sulfate, concentrated and the crude was purified by normal phase (ethyl acetate/hex) chromatography. The fractions containing the product were combined and concentrated to give an off-white solid (160 mg).
MS (ESP): 357(M+2) for C15H23BrN4O.
The following compounds have been synthesized as described for Intermediate 249 from the starting materials indicated in the table below.
1-(4-Bromopyridin-2-yl)-3-ethylurea (Intermediate 14, 500 mg, 2.05 mmol), 3,3-dimethylpiperidine (301 mg, 2.66 mmol), copper(I) iodide (39.0 mg, 0.20 mmol) and pyrrolidine-2-carboxylic acid (47.2 mg, 0.41 mmol) and potassium carbonate (566 mg, 4.10 mmol) were taken in a round bottomed flask and degassed with argon. DMSO (8 mL) was added, and the mixture was degassed with argon again, then heated at 105° C. for 4 h. The reaction was partitioned between water and ethyl acetate. The layers were separated and the aqueous was extracted with ethyl acetate. The combined extract was washed with water and brine, dried over magnesium sulfate and concentrated. The crude was purified by normal phase (Hex/ethyl acetate) chromatography to give an off-white solid (200 mg).
MS (ESP): 277 (M+1) for C15H24N4O
The following compounds have been synthesized as described for Intermediate 253 from the starting materials indicated in the table below.
To a solution of 1-ethyl-3-(5′-(hydrazinecarbonyl)-4-(3-(trifluoromethyl)-1H-pyrazol-1-yl)-3,3′-bipyridin-6-yl)urea (Intermediate 238, 80 mg, 0.18 mmol) in DMF (3 mL), DIPEA (0.032 mL, 0.18 mmol) was added followed by (S)-2-(tert-butoxycarbonylamino)-3-methylbutanoic acid (40.0 mg, 0.18 mmol) and HATU (180 mg, 0.47 mmol) and the solution was stirred for 30 min at RT. The reaction was partitioned between water and ethyl acetate. The layers separated and the aqueous layer was back extracted with ethyl acetate twice. Then the combined extracts were washed with water and brine, dried over magnesium sulfate and concentrated to give a clear oil. The oil was taken up in acetonitrile (5 mL) and DBU (0.042 mL, 0.28 mmol) was added followed by triphenylphosphine (97 mg, 0.37 mmol) and carbon tetrachloride (0.036 mL, 0.37 mmol). The resulting solution was stirred at room temperature overnight. The reaction was concentrated and the crude was partitioned between water and ethyl acetate. The layers separated and the aqueous was back extracted twice. The combined extracts were washed with water and dried over magnesium sulfate, concentrated and purified by normal phase (hex/ethyl acetate) chromatography to give a white solid (95 mg) which was slurried in acetonitrile, and filtered and dried (65 mg white solid).
MS (ESP): 616 (M+1) for C28H32F3N9O4
To a suspension of 1-ethyl-3-(5′-(hydrazinecarbonyl)-4-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridin-6-yl)urea (Intermediate 9, 70 mg, 0.16 mmol) in acetonitrile (3 mL), potassium carbonate (25.7 mg, 0.19 mmol) was added, followed by a slow addition of cyclopropanecarbonyl chloride (0.014 mL, 0.16 mmol) and the resulting mixture was stirred at room temperature for 30 minutes. The precipitated product was filtered and the residue was washed with acetonitrile and water to give 72 mg of the desired product as a tan colored solid.
MS (ESP): 520 (M+1) for C22H20F3N7O3S. Intermediates 259-260
The following Intermediates were prepared by the general procedure described below from the starting materials indicated in the Table.
A suspension of ester (0.3 g, 6 mmol, 1 eq) in the corresponding alcohol (2-3 mL, ˜50 equiv.) in a small vial was stirred for 2 min at room temperature. Sodium hydride (0.150 g, 60 mmol) was added over 5 min and the reaction was stirred for a further 5 h at room temperature. The reaction was cooled with an ice bath and slowly quenched with HCl (0.1N) solution until pH 7. The aqueous layer was extracted twice with ether to remove excess alcohol. The aqueous layer was concentrated in vacuo to almost dryness than loaded on Analogix C18-column for reverse phase purification (water-methanol) to remove excess salt.
To a slurry of 6-(3-propylureido)-4-(4-trifluoromethylthiazol-2-yl)pyridin-3-ylboronic acid (Intermediate 218, 0.63 g, 1.7 mmol), tetrahydro-2H-pyran-4-yl 5-bromo-6-(tetrahydro-2H-pyran-4-yloxy)nicotinate (Intermediate 281, 0.5 g, 1.3 mmol) and trans dichlorobis(triphenylphosphine)palladium (II) (597 mg, 0.85 mmol) in 1,4-dioxane (72 mL) was added a solution of potassium carbonate (2.4 g, 17.0 mmol) in water (27 mL). The reaction was stirred at 70° C. for 1 h. The reaction was cooled to room temperature, and ethyl acetate (100 mL) and water (10 mL) were added to help separate the layers. The water was removed, and the organic phase was washed with water (10 mL). The reaction was then concentrated and the residue was triturated with a mixture of ethanol (20 mL) and methyl tert-butyl ether (50 mL). The solid was dried in a vacuum oven at 50° C. for 3 hours. This gave tetrahydro-2H-pyran-4-yl 6′-(3-propylureido)-2-(tetrahydro-2H-pyran-4-yloxy)-4′-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridine-5-carboxylate (˜80% yield) as an off white solid.
MS (ESP): 635.20 (MH+) for C29H32F3N5O6S.
Tetrahydro-2H-pyran-4-yl 6′-(3-propylureido)-2-(tetrahydro-2H-pyran-4-yloxy)-4′-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridine-5-carboxylate (Intermediate 261, ˜0.3 mmol) was dissolved in tetrahydrofuran-water and treated with lithium hydroxide (10 eq) at room temperature for 24 h. After this period of time, the organic was removed under vacuum. Dilute HCl was added to adjust the pH to 7 and the aqueous layer was extracted with ethyl acetate. The organic layer was dried over sodium sulfate and concentrated to dryness to give the corresponding acid which was used directly for the next step.
MS (ESP): 552.1 (MH+) for C24H24F3N5O5S
1-(5-bromo-4-(4-(trifluoromethyl)thiazol-2-yl)pyridin-2-yl)-3-propylurea (Intermediate 218, 200 mg, 0.51 mmol), methyl 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)nicotinate (173 mg, 0.65 mmol), and trans dichlorobis(triphenylphosphine)palladium (II) (36 mg, 0.05 mmol) were dissolved in 1,4-dioxane (8 mL). Sodium bicarbonate (170 mg, 2 mmol) was dissolved in water (3 mL) and added to the above mixture. The reaction was heated at 65° C. for 60 min. Ethyl acetate (10 mL) was then added to the reaction and the layers were separated. The solvent was removed in vacuo and the residue was triturated with ethanol (5 mL). The solid was dried in a vacuum oven at 60° C. for 1 hour to give 145 mg (64% yield) of methyl 6′-(3-propylureido)-4′-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridine-5-carboxylate as an off white powder.
MS (ESP): 466.2 (M+H+) for C20H18F3N5O3S
1H NMR (300 MHz, DMSO-d6): δ 0.88 (t, 3H), 1.49 (m, 2H), 3.17 (m, 2H), 3.87 (s, 3H), 7.59 (bt, 1H), 8.20 (s, 1H), 8.21 (s, 1H), 8.37 (s, 1H), 8.37 (s, 1H), 8.75 (d, 1H), 9.07 (d, 1H), 9.54 (bs, 1H).
6-(3-Propylureido)-4-(4-(trifluoromethyl)thiazol-2-yl)pyridin-3-ylboronic acid (Intermediate 218, 200 mg, 0.54 mmol), diethyl 2-chlorothiazole-4,5-dicarboxylate (110 mg, 0.41 mmol), and trans dichlorobis(triphenylphosphine)palladium (II) (30 mg, 0.041 mmol) were dissolved in 1,4-dioxane (8 mL). Sodium bicarbonate (170 mg, 2 mmol) was dissolved in water (3 mL) and added to the above mixture. The reaction was heated at 80° C. in a microwave for 60 min. Ethyl acetate (10 mL) was then added to the reaction and the layers were separated. The solvent was removed in vacuo and the residue was chromatographed on an Analogix 4 g column using 1-100% ethyl acetate in heptane. This gave 73 mg (31% yield) of diethyl 2-(6-(3-propylureido)-4-(4-(trifluoromethyl)thiazol-2-yl)pyridin-3-yl)thiazole-4,5-dicarboxylate as an off white powder.
MS (ESP): 558.2 (M-FH') for C22H22F3N5O5S2
6-(3-Propylureido)-4-(4-(trifluoromethyl)thiazol-2-yl)pyridin-3-ylboronic acid (Intermediate 218, 311 mg, 0.86 mmol), methyl 4-chloropicolinate (135 mg, 0.78 mmol), and trans dichlorobis(triphenylphosphine)palladium (II) (32 mg, 0.04 mmol) were dissolved in 1,4-dioxane (4 mL). Sodium bicarbonate (131 mg, 1.5 mmol) was dissolved in water (1 mL) and added to the above mixture. The reaction was heated at 80° C. for 60 min in the microwave. Ethyl acetate (10 mL) was then added to the reaction and the layers were separated. The solvent was removed in vacuo and the residue was chromatographed on an Analogix 4 g column using 0-100% ethyl acetate in heptane. The solid was dried in a vacuum oven at 60° C. for 1 hour to give 102 mg (26% yield) of methyl 6-(3-propylureido)-4-(4-(trifluoromethyl)thiazol-2-yl)-3,4′-bipyridine-2′-carboxylate as an off white powder.
MS (ESP): 466.2 (M+H+) for C20H18F3N5O3S
To a suspension of 1-ethyl-3-(5′-(5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)-4-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridin-6-yl)urea (Example 6, 235 mg, 0.49 mmol) in ethanol (3 mL) was added azetidin-3-ol (162 mg, 1.48 mmol) followed by TEA (0.206 mL, 1.48 mmol) and heated to 100° C. for 2 h in a microwave. The reaction mixture was concentrated and used without further purification.
The title compound was synthesized by method analogous to Intermediate 266 starting with Example 6 and (R)-pyrrolidin-3-ol.
The title compound was synthesized by method analogous to Intermediate 266 starting with Example 6 and (S)-pyrrolidin-3-ol.
The title compound was synthesized by method analogous to Intermediate 266 starting with Example 6 and piperidin-4-ol.
The title compound was synthesized by method analogous to Intermediate 266 starting with Example 6 and piperidin-3-ol.
To a solution of 1-ethyl-3-(5′-(hydrazinecarbonyl)-4-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridin-6-yl)urea (Intermediate 9, 340 mg, 0.75 mmol) in DMF (5 mL) was added (S)-2-(tert-butoxycarbonylamino)-3-methylbutanoic acid (245 mg, 1.13 mmol), HATU (573 mg, 1.51 mmol) and DIEA (0.329 mL, 1.88 mmol). After stirring overnight, the reaction mixture was diluted with water and extracted with EtOAc (2×). The combined organic layers were washed with brine, dried (Na2SO4) and concentrated to give light yellow color solid.
The title compound was synthesized by method analogous to Intermediate 271 starting with Intermediate 9 and (R)-2-(tert-butoxycarbonylamino)-3-methylbutanoic acid.
The following Intermediates were prepared according to the procedure described for Intermediate 28 from the starting materials indicated in the Table.
In a dried 250 mL glass round bottom flask, sodium hydride (0.878 g, 21.96 mmol) was suspended in 20 mL of anhydrous DMF. Tetrahydro-2H-pyran-4-ol (1.838 mL, 19.32 mmol) was added to the suspension dropwise. Upon reacting, the suspension became homogenous and a clear yellow solution was obtained. Methyl 5-bromo-6-chloronicotinate (2.2 g, 8.78 mmol) was then added in a single portion. The resultant reaction mixture was stirred at room temperature for 1 hour. A brown precipitate began to form. The reaction was monitored by LC/MS and TLC (6:4 EtOAc/hexanes). When the reaction was complete the mixture was diluted with Et2O, cooled to 0° C. (ice bath) and slowly quenched with water. The aqueous and organic phases were separated and the organic layer was dried over Na2SO4, filtered, concentrated by rotary evaporation and purified by flash column chromatography (1:1 EtOAc/hexanes). Isolation gave 441 mg of desired product.
LC/MS (ES+): 386, 388 for C16H20BrNO5.
The following Intermediates were prepared according to the procedure described for Intermediate 51 using the starting material indicated in the table.
5-bromo-2-(3-ethylureido)isonicotinic acid (Intermediate 51, 6.25 g, 21.69 mmol) was dissolved in a DMF (60 mL) solution containing HATU (12.38 g, 32.54 mmol) and DIEA (7.54 mL, 43.39 mmol). After the mixture was stirred for 15 min, benzohydrazide (3.25 g, 23.86 mmol) was added in a single portion and the reaction mixture was stirred at room temperature for 1 h, the heated to 70° C. for 1 hour. Solids precipitated from solution. The reaction was not complete after 12 hours, so another 2 grams of HATU was added and the mixture was heated until the reaction was complete. The reaction mixture was cooled to room temperature. The solids were filtered and washed with minimal DMF. The solids were then triturated in water, filtered and dried in vacuo. Isolation gave 3 grams of a white fluffy solid. LC/MS (ES+): 406, 408 for C16H16BrN5O3.
1H NMR (300 MHz, d6-DMSO): 1.09 (t, 3H), 3.18 (m, 2H), 7.33 (t, 1H), 7.53 (m, 3H), 7.85 (s, 1H), 7.93 (d, 2H), 8.42 (s, 1H), 9.42 (s, 1H), 10.60 (s, 1H), 10.67 (s, 1H).
The following Intermediate was prepared according to the procedure described for Intermediate 285 using the starting materials indicated in the table.
1-(4-(2-benzoylhydrazinecarbonyl)-5-bromopyridin-2-yl)-3-ethylurea (Intermediate 285, 4.73 g, 11.64 mmol) was suspended in a methylene chloride (20 mL) solution containing triphenyl phosphine (3.36 g, 12.81 mmol), carbon tetrabromide (4.25 g, 12.81 mmol) and triethylamine (1.790 mL, 12.81 mmol) (pre-mixed and stirred for 10 minutes). The mixture was stirred at room temperature and monitored by LC/MS. The reaction was not complete after 12 hours, so a second CH2Cl2 (20 mL) solution containing triphenyl phosphine (3.36 g, 12.81 mmol), carbon tetrabromide (4.25 g, 12.81 mmol) and triethylamine (1.790 mL, 12.81 mmol) was prepared and added to the reaction mixture. This procedure was repeated a third time. Once the reaction was deemed complete, the precipitate was filtered off, and washed with CH2Cl2. The filtration yielded 970 mg of the product. The mother liquor was purified by flash column chromatography (95:5 CH2Cl2/MeOH). Isolation gave another 1.2 gram of product. Total isolated weight was 2.1 g.
LC/MS (ES+): 388, 340 for C16H14BrN5O2.
1H NMR (300 MHz, d6-DMSO): 1.09 (t, 3H), 3.19 (m, 2H), 7.21 (t, 1H), 7.66 (m, 2H), 7.69 (s, 1H), 8.08 (m, 2H), 8.45 (s, 1H), 8.61 (s, 1H), 9.49 (s, 1H).
The following Intermediate was prepared according to the procedure described for Intermediate 287 using the starting materials indicated in the table.
Ethyl 2-(4-carbamoyl-6-(3-ethylureido)pyridin-3-yl)-4-(pyrimidin-2-yl)thiazole-5-carboxylate (Intermediate 319, 132 mg, 0.30 mmol) was suspended in THF. Lawesson's reagent (145 mg, 0.36 mmol) was added in a single portion. The suspension was heated to reflux for 1 h. The reaction mixture concentrated to dryness.
LC/MS (ES+)[(M+H)+]: 458 for C19H19N7O3S2.
The following Intermediates were prepared according to the procedure described for Intermediate 16 using the starting materials indicated.
1-(5-Bromo-4-(5-phenyl-1,3,4-oxadiazol-2-yl)pyridin-2-yl)-3-ethylurea (Intermediate 287, 1.17 g, 3.01 mml) and PdCl2(PPh3)2 (0.2 g, 0.3 mmol) were suspended in 1,4 dioxane. The reaction mixture was degassed and purged with nitrogen. The suspension was gently warmed to 70° C. 4,4,4′,4′,5,5,5′,5′-Octamethyl-2,2′-bi(1,3,2-dioxaborolane) (2.3 g, 9.04 mmol) was added in a single portion and the mixture was stirred at 100° C. for 30 min. Triethylamine (0.91 g, 9.04 mmol) was added followed by KOAc (0.88 g, 9.04 mmol). The reaction mixture was then allowed to react for 12 hours, then the reaction was cooled to room temperature, filtered through a pad of Celite, and the mother liquor was concentrated to dryness. The residue was dissolved in ethyl acetate and the solution was washed with water, dried over Na2SO4, filtered and concentrated to a solid. The solid was triturated in EtOAc, filtered and dried in vacuo (isolated ˜925 mg's). The mother liquor was concentrated further and then purified by flash column chromatography (0-100% EtOAc/hexanes) to give an additional 60 mg of product. Isolated weight and approximate purity as judged by LC/MS ratios (1:1 ratio of ester and acid): 925 mg (95% pure).
LC/MS (ES+)[(M+H)+]: 436 for C22H26BN5O4 (Boronic ester); 354 for C16H16BN5O4 (Boronic acid).
The following Intermediates were prepared by the procedure described for Intermediate 300 using the starting materials indicated in the table.
In a sealed microwave vessel, methyl 2-(3-ethylureido)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)isonicotinate (Intermediate 301, 1.2 g, 3.44 mmol) was dissolved in a methanol solution containing ammonia (7N) (10 mL, 70.00 mmol). The solution was heated at 80° C. for 15 minutes, the concentrated to dryness. The product was used without further purification.
LC/MS (ES+)[(M+H)+]: 369 for C9H13BN4O4.
The following Intermediates were prepared according to the procedure described for Intermediate 2 using the starting materials indicated in the table.
Methyl 2-amino-5-bromoisonicotinate (20 g, 86.56 mmol) was suspended in CHCl3 (20 mL). Ethyl isocyanate (10.20 mL, 129.84 mmol) was added in a single portion and the reaction was heated in an oil bath to 80° C. for 5 h. The reaction mixture was concentrated to dryness by rotary evaporation. The product crystallized from a mixture of CH2Cl2 and hexanes. Isolation gave 16.2 grams of the title compound.
LC/MS (ES+): 302, 304 for C10H12BrN3O3.
1H NMR (300 MHz, d6-DMSO): 1.07 (t, 3H), 3.18 (m, 2H), 3.89 (s, 3H), 7.18 (t, 1H), 8.02 (s, 1H), 8.46 (s, 1H), 9.42 (s, 1H).
The following Intermediates were prepared according to the procedure described for Intermediate 2 using the starting materials indicated in the table.
Methyl 6′-(3-ethylureido)-2-fluoro-4′-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridine-5-carboxylate (Intermediate 162, 200 mg, 0.43 mmol) was added to a THF solution containing sodium hydride (85 mg, 2.13 mmol). The mixture was stirred at room temperature for 18 h. The reaction was neutralized with 2N HCl. The reaction mixture was concentrated to dryness by rotary evaporation. Purified by silica gel flash column chromatography (95:5 CH2Cl2/MeOH) gave 220 mg of the title compound.
LC/MS (ES+)[(M+H)+]: 551 for C24H25F3N6O4S.
cyclopropylmethyl 2-(cyclopropylmethoxy)-6′-(3-ethylureido)-4′-(4-(1-methyl-1H-pyrazol-4-yl)thiazol-2-yl)-3,3′-bipyridine-5-carboxylate
Lithium bis(trimethylsilyl)-amide (0.841 mL, 0.84 mmol) was added to solution of cyclopropylmethanol (0.033 mL, 0.42 mmol) in THF (1.5 mL). Methyl 6′-(3-ethylureido)-2-fluoro-4′-(4-(1-methyl-1H-pyrazol-4-yl)thiazol-2-yl)-3,3′-bipyridine-5-carboxylate (Intermediate 334, 0.081 g, 0.17 mmol) was added after 30 min. The mixture was stirred at room temperature overnight. The reaction was quenched with NH4OH, partitioned between water and ethyl acetate, the layers were separated, and the organic phase was washed with water and brine, dried over magnesium sulfate, concentrated under reduced pressure, and purified by column chromatography (Silica gel, 0-10% MeOH in CH2Cl2) to give 59 mg of crude compound.
LC/MS (ES+)[(M+H)+]: 574 for C29H31N7O4S.
The following Intermediates were prepared according to the procedure described for Intermediate 337 using the starting materials indicated in the table.
The following Intermediates were prepared according to the procedure described Intermediate 9 using the starting material indicated in the table.
6′-(3-ethylureido)-2-(2-(pyrrolidin-1-yl)ethoxy)-4′-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridine-5-carboxylic acid (Intermediate 336, 220 mg, 0.40 mmol) was dissolved in a DMF solution containing HATU (152 mg, 0.40 mmol) and diisopropylethyl amine (0.139 mL, 0.80 mmol). The solution was stirred for 30 minutes. Hydrazine (0.015 mL, 0.48 mmol) was added in a single portion. The reaction mixture was stirred for 0.5 hour. The reaction mixture was diluted with EtOAc, washed with water and brine, dried over Na2SO4, filtered and concentrated to give the title compound which was used without further purification.
LC/MS (ES+)[(M+H)+]: 565 for C24H27F3N8O3S.
The following Intermediates were prepared according to the synthesis described for Intermediate 387 using the starting materials indicated in the table.
In a glass vial, 1-ethyl-3-(5′-(hydrazinecarbonyl)-4-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridin-6-yl)urea (Intermediate 9, 300 mg, 0.66 mmol) and (S)-2-(tert-butoxycarbonylamino)-2-cyclohexylacetic acid (188 mg, 0.73 mmol) were combined and dissolved in a DMF solution containing diisopropylethyl amine (0.173 mL, 1.00 mmol). The reaction mixture was stirred for 5 min, then HATU (329 mg, 0.86 mmol) was added in a single portion. The reaction mixture was diluted with EtOAc, washed with water and brine, dried over Na2SO4, filtered and concentrated to a residue which was purified by silica gel flash column chromatography (95:5 CH2Cl2/MeOH).
LC/MS (ES+)(M+H)+: 691 for C31H37F3N8O5S.
The following Intermediates were prepared according to the procedure described for Intermediate 392 using the starting materials indicated in the table.
(S)-1-ethyl-3-(5′-(2-(2-hydroxypropanoyl)hydrazinecarbonyl)-4-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridin-6-yl)urea (Intermediate 402, 260 mg, 0.50 mmol) was suspended in a CH2Cl2 (10 mL) solution containing 2,6-lutidine (213 mg, 1.99 mmol). The suspension was cooled to 0° C. (ice-water bath). Triethylsilyl trifluoromethanesulfonate (0.337 mL, 1.49 mmol) was added in a single portion via a micro syringe. The reaction mixture was slowly warmed to room temperature where it was allowed to react for 5 h. The reaction mixture became homogeneous, and analysis showed complete conversion to the silyl protected compound. The reaction mixture was diluted with CH2Cl2, washed with NaHCO3 (sat.) and brine, dried organic over Na2SO4, filtered and concentrate by rotary evaporation. The crude reaction mixture was purified by silica gel flash column chromatography (95:5 CH2Cl2 MeOH) to give 205 mg of the title compound.
LC/MS (ES+)[(M+H)+]: 638 for C27H34F3N7O4SSi.
In a glass vial, (S)-tert-butyl 1-cyclohexyl-2-(2-(6′-(3-ethylureido)-4′-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridine-5-carbonyl)hydrazinyl)-2-oxoethylcarbamate (Intermediate 392, 459 mg, 0.66 mmol) was dissolved in a ACN solution containing carbon tetrachloride (0.321 mL, 3.32 mmol) and DBU (1,8-Diazabicyclo[5.4.0]-undec-7-ene) (0.497 mL, 3.32 mmol). Triphenyl phosphine (349 mg, 1.33 mmol) was added in a single portion, and the reaction mixture was stirred at room temperature overnight. The reaction mixture was diluted with EtOAc, washed with water/brine, dried over Na2SO4, filtered and concentrated to dryness by rotary evaporation. The concentrate was purified by silica gel flash column chromatography (95:5 CH2Cl2/MeOH).
LC/MS (ES+)[(M+H)+]: 673 for C31H35F3N8O4S.
1H NMR (300 MHz, d6-DMSO): 0.95-1.45 (m, 6H), 1.12 (t, 3H), 1.37 (s, 9H), 1.62-1.89 (m, 5H), 3.22 (m, 2H), 4.71 (m, 1H), 7.55 (t, 1H), 7.66 (d, 1H), 8.25 (s, 1H), 8.27 (s, 1H), 8.42 (s, 1H), 8.56 (s, 1H), 8.73 (s, 1H), 9.18 (s, 1H), 9.51 (s, 1H).
The following Intermediates were prepared according to the procedure described for Intermediate 404 using the starting materials indicated in the table.
In a microwave vessel, 5-bromoisobenzofuran-1,3-dione (500 mg, 2.20 mmol) was suspended in an ethanolic solution containing 2-hydrazinylethanol (0.332 mL, 4.41 mmol). The vial was sealed and heated to reflux. The reaction mixture became homogeneous upon heating. After for 12 hours, the reaction was cooled to room temperature. Solids precipitated from solution and were collected by filtration, washed with ethanol, and dried in vacuo. Analysis showed the ratio of desired products to be 1:1 with about 30% of an unidentified side product. Isolation gave 340 mg of a 1:1 mixture of the title compounds which were not further purified.
LC/MS (ES+)[(M+H)+]: 285, 287 for C10H9BrN2O3.
The title compound was prepared as described for Intermediate 2 from Intermediate 12 and Intermediate 349.
LC/MS (ES+)[(M+H)+]: 633 for C30H35F3N6O4S.
The title compound was prepared as described for Intermediate 9 from Intermediate 413 and hydrazine hydrate.
LC/MS (ES+)[(M+H)+]: 591 for C26H29F3N8O3S
DMSO (36 mL) was added to a dry suspension of 1-(5-bromo-4-(4-(6-methoxypyridin-2-yl)thiazol-2-yl)pyridin-2-yl)-3-ethylurea (Intermediate 293, 2.5 g, 5.76 mmol), PdCl2(dppf)-CH2Cl2 adduct (430 mg, 0.53 mmol), 4,4,4′,4′,5,5,5′,5′-octamethyl-2,2′-bi(1,3,2-dioxaborolane) (3 g, 11.81 mmol), and potassium acetate (1 g, 10.19 mmol) under vacuum. The resulting suspension was warmed to 80° C. and treated with triethyl amine (1 ml, 7.17 mmol) and stirred under nitrogen at this temperature for 16 hours. The reaction was diluted with water (100 ml), and held at 100° C. for 1 hr, cooled to room temperature, and filtered to give crude product as a peach filter cake. This material was suspended in ethyl acetate (200 ml), warmed to 70° C. for 1 hour, and filtered hot to give (1.44 g, 62.7%) of a peach solid as a 3:1 mixture of title boronic acid and the reduced material.
MS (EI) (M+H)+ 400 for C17H19BN5O4S (M−H)− 398 for C17H17BN5O4S
1H NMR (DMSO-d6) δ: 8.41 (t, J=5.46 Hz, 1H), 8.25 (s, 1H), 7.96 (s, 1H), 7.86 (s, 1H), 7.77 (d, J=7.16 Hz, 1H), 6.84 (d, J=7.72 Hz, 1H), 3.97 (s, 3H), 3.21 (d, J=7.35 Hz, 2H), 1.08-1.14 (m, 3H).
Intermediate 416 was synthesized according to the procedure described for intermediate 22 from Intermediate 417 and hydrazine.
MS (EI) (M+H)+ 491 for C23H23N8O3S (M−H)− 489 for C23H21N8O3S;
A mixture of 6-(3-ethylureido)-4-(4-(6-methoxypyridin-2-yl)thiazol-2-yl)pyridin-3-ylboronic acid (Intermediate 415, 400 mg, 1.00 mmol), methyl 4-bromopicolinate (216 mg, 1.00 mmol), dicyclohexyl(2′,4′,6′-triisopropylbiphenyl-2-yl)phosphine (143 mg, 0.30 mmol), Pd2 dba3 (45.9 mg, 0.05 mmol) and Cs2CO3 (392 mg, 1.20 mmol), under vacuum was treated with 1,4-dioxane (20 mL) and water (5 mL). The reaction mixture was placed in oil bath at 80° C., and held at that temperature for 2 hours, The reaction was cooled to room temperature, diluted with ethyl acetate (100 ml), water (50 ml), and brine (5 ml), and the layers were separated. The aqueous phase was extracted with ethyl acetate (3×50 ml), and the combined organic layers were washed with brine, dried over sodium sulfate, filtered, and the solvents were removed under reduced pressure. The resulting residue was purified by chromatography on silica gel eluting with a gradient of methanol in methylene chloride. The major peak was concentrated, and precipitated by the addition of acetonitrile to give the title compound as a tan solid (480 mg, 98%)
MS (EI) (M+H)+ 491 for C23H23N6O4S (M−H) 489 for C23H21N6O4S
1H NMR (DMSO-d6) δ: 9.52 (s, 1H), 8.72 (d, J=4.90 Hz, 1H), 8.35-8.37 (m, 1H), 8.33 (br. s., 1H), 8.21 (s, 1H), 8.01 (s, 1H), 7.71 (t, J=7.82 Hz, 1H), 7.63 (d, J=5.09 Hz, 1H), 7.58 (t, J=5.18 Hz, 1H), 7.16 (d, J=7.35 Hz, 1H), 6.78 (d, J=8.10 Hz, 1H), 3.91 (s, 3H), 3.84 (s, 3 H), 3.22 (tt, J=7.16, 6.40 Hz, 2H), 1.11 (t, J=7.06 Hz, 3H).
A suspension of 5-bromonicotinohydrazide (Intermediate 433, 2.3 g, 10.65 mmol) in 1,1,1-trimethoxyethane (20 ml, 166.46 mmol) was heated reflux and treated with concentrated aqueous HCl (drop), the resulting clear colorless solution was refluxed for 20 minutes, treated with DBU (0.2 ml, 1.33 mmol) and refluxed an additional 20 min. The material was concentrated under reduced pressure to give a tan gum which was purified by flash chromatography on silica gel eluting with a gradient of ethyl acetate in hexanes to give the title compound as a white solid (2.47 g, 97%)
MS (EI) (M+H)+ 240/242 for C8H7BrN3O
1H NMR (DMSO-d6) δ: 9.10 (d, J=1.51 Hz, 1H), 8.93 (d, J=2.07 Hz, 1H), 8.52 (t, J=1.60 Hz, 1H), 2.61 (s, 3H);
13C NMR (DMSO-d6) δ: 164.75 (s, 1 C), 160.98 (s, 1 C), 152.90 (s, 1 C), 145.43 (s, 1 C), 135.97 (s, 1 C), 121.60 (s, 1 C), 120.58 (s, 1 C), 10.61 (s, 1 C).
A solution of crude methyl 2-(6-(3-ethylureido)-4-(4-(6-methoxypyridin-2-yl)thiazol-2-yl)pyridin-3-yl)-4-(1-methyl-1H-1,2,4-triazol-5-yl)thiazole-5-carboxylate (Intermediate 420, 250 mg, 0.43 mmol) in ethanol was treated with hydrazine (0.5 mL, 0.43 mmol), and the pale grey solution was heated to reflux for 16 hours. The resulting pale grey suspension was filtered to give the title compound as a grey solid (200 mg, 0.35 mmol, 80%).
MS (EI) (M+H)+ 578 for C24H24N11O3S2) (M−H)− 576 for C24H22N11O3S2
1H NMR (DMSO-d6) δ: 11.81 (br. s., 1H), 9.68 (s, 1H), 8.82 (s, 1H), 8.47 (s, 1H), 8.24 (s, 1H), 8.12 (s, 1H), 7.74 (t, J=7.72 Hz, 1H), 7.56 (br. s., 1H), 7.42 (d, J=7.35 Hz, 1H), 6.81 (d, J=8.29 Hz, 1H), 3.95 (d, J=3.01 Hz, 6H), 3.12-3.26 (m, 2H), 1.09-1.16 (m, 3H).
1,4-Dioxane (20 mL) and water (5 mL) were added to a mixture of 6-(3-ethylureido)-4-(4-(6-methoxypyridin-2-yl)thiazol-2-yl)pyridin-3-ylboronic acid (Intermediate 415, 400 mg, 1.00 mmol), methyl 2-chloro-4-(1-methyl-1H-1,2,4-triazol-5-yl)thiazole-5-carboxylate (Intermediate 44, 259 mg, 1.00 mmol), Pd2 dba3 (45.9 mg, 0.05 mmol), dicyclohexyl(2′,4′,6′-triisopropylbiphenyl-2-yl)phosphine (143 mg, 0.30 mmol), and Cs2CO3 (392 mg, 1.20 mmol), under vacuum. The suspension was placed in oil bath at 80° C., purged with nitrogen, and heated for 30 minutes. When the reaction was complete by LCMS, it was cooled to room temperature, diluted with water (100 ml), and extracted with ethyl acetate (4×75 ml). The combined organic layers were washed with brine, dried over sodium sulfate, filtered, and concentrated under reduced pressured, and the residue was purified by silica gel chromatography eluting with a gradient of methanol in methylene chloride to give the title compound as a beige solid (265 mg, 0.46 mmol, 45.8%).
MS (EI) (M+H)+ 578 for C25H23N9O4S2 (M−H)− 576 for C25H21N9O4S2
1H NMR (DMSO-d6) δ: 9.71 (s, 1H), 8.78 (s, 1H), 8.48 (s, 1H), 8.17 (s, 1H), 8.06 (s, 1H), 7.75 (t, J=7.82 Hz, 1H), 7.49 (br. s., 1H), 7.43 (d, J=7.35 Hz, 1H), 6.81 (d, J=8.10 Hz, 1H), 3.95 (s, 3H), 3.74 (s, 3H), 3.65 (s, 3H), 3.10-3.28 (m, 2H), 1.11 (t, J=7.16 Hz, 3H);
Intermediate 421 was synthesized according to the procedure described for Intermediate 22 from Intermediate 422 and hydrazine.
MS (EI) (M+H)+475 for C23H23N8O2S (M−H)− 473 for C23H21N8O2S;
1H NMR (DMSO-d6) δ: 9.98 (s, 1H), 9.45 (s, 1H), 8.97 (d, J=1.88 Hz, 1H), 8.52 (d, J=1.88 Hz, 1H), 8.41 (d, J=5.84 Hz, 2H), 8.28 (s, 1H), 8.09 (s, 2H), 7.66 (t, J=4.99 Hz, 1H), 7.53 (s, 1H), 7.08 (d, J=5.65 Hz, 2H), 4.59 (br. s., 2H), 4.03 (s, 2H), 3.20 (quin, J=6.97 Hz, 2H), 1.10 (t, J=7.16 Hz, 3H)
Intermediate 422 was synthesized as described for Intermediate 20 from Intermediate 423 and ethyl 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)nicotinate.
MS (EI) (M+H)+489 for C25H25N6O3S (M−H) 487 for C25H23N6O3S;
1H NMR (DMSO-d6) δ: 9.46 (s, 1H), 9.02 (d, J=2.07 Hz, 1H), 8.67 (d, J=2.26 Hz, 1H), 8.38 (d, J=5.46 Hz, 2H), 8.29 (s, 1H), 8.01-8.12 (m, 2H), 7.66 (t, J=5.27 Hz, 1H), 7.57 (s, 1H), 7.03 (d, J=5.65 Hz, 2H), 4.32 (q, J=6.78 Hz, 2H), 3.99 (s, 2H), 3.18-3.25 (m, 2 H), 1.31 (t, J=7.06 Hz, 3H), 1.10 (t, J=7.16 Hz, 3H).
A solution of 1-bromo-3-(pyridin-4-yl)propan-2-one hydrobromide (Intermediate 424, 434 mg, 1.47 mmol) and 5-bromo-2-(3-ethylureido)pyridine-4-carbothioamide (Intermediate 5, 500 mg, 1.65 mmol) in ethanol (25 mL) was heated to reflux for 1 hour. The mixture was then cooled, diluted with water (100 ml), ethyl acetate (100 ml) and saturated aqueous sodium hydrogen carbonate, the layers were separated and the aqueous phase extracted with ethyl acetate (3×100 ml). The combined organic layers were washed with brine, dried over magnesium sulfate, filtered, concentrated under reduced pressure, and the resulting residue was purified by normal phase chromatography on silica gel, eluting with a gradient of ethyl acetate in hexanes to afford as a tan solid after trituration from dichloromethane with hexanes 364 mg (59%) of the title compound as a pale yellow powder.
MS (EI) (M+H)+ 418/420 for C17H17BrN5OS (M−H)− 416/418 for C17H15BrN5OS;
1H NMR (DMSO-d6) δ: 9.36 (s, 1H), 8.45-8.56 (m, 3H), 8.33 (s, 1H), 7.75 (s, 1H), 7.28-7.40 (m, 3H), 4.23 (s, 2H), 3.17 (quin, J=6.64 Hz, 2H), 1.08 (t, J=7.16 Hz, 3H);
Bromine (0.65 ml, 12.5 mmol) was added to a solution of 1-(pyridin-4-yl)propan-2-one (770 mg, 5.70 mmol) in HBr (10 mL, 184.15 mmol, 33% in acetic acid). After 5 hours, the reaction was diluted with acetone (40 ml) and the resulting solution was stirred at room temperature for 19 hours. The resulting tan suspension was filtered to afford as a tan solid 755 mg of the title compound as a 2:1 mixture with 1,3-dibromo-1-(pyridin-4-yl)propan-2-one.
MS (EI) (M+H)+ 214/216 for C8H9BrNO
1H NMR (DMSO-d6) δ: 8.82-8.95 (m, 2H), 8.65 (d, J=6.22 Hz, 1H), 8.05 (d, J=6.03 Hz, 1H), 7.92 (d, J=6.03 Hz, 2H), 5.89 (s, 1H), 4.57 (s, 2H), 4.38 (s, 1H), 4.30 (s, 2H)
A mixture of ethyl 5-bromo-2-(2-methoxyethoxy)nicotinate (Intermediate 426, 500 mg, 1.64 mmol), 1-ethyl-3-(5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-4-(4-(trifluoromethyl)thiazol-2-yl)pyridin-2-yl)urea (Intermediate 12, 500 mg, 1.13 mmol), Cs2CO3 (370 mg, 1.14 mmol), Pd2dba3 (27 mg, 0.03 mmol), and dicyclohexyl triisopropylbiphenylphosphine (170 mg, 0.36 mmol) in 1,4-dioxane (12 mL) was degassed, treated with water (3.00 mL), and then heated to 80° C. for 30 minutes. The reaction mixture was diluted with water (100 ml), brine (10 ml), and ethyl acetate (100 ml), and the layers were separated. The aqueous phase was extracted with ethyl acetate (3×50 ml), and the combined organics were washed with brine, dried over magnesium sulfate, filtered, concentrated under reduced pressure and purified by normal phase chromatography eluting with a gradient of ethyl acetate in hexanes to afford 90 mg of the title compound as a pale amber oil, which was used without further purification.
MS (EI) (M+H)+ 540 for C23H25F3N5O5S (M−H) 538 for C23H23F3N5O5S.
A solution of 5-bromo-2-(2-methoxyethoxy)nicotinic acid (Intermediate 427, 800 mg, 2.90 mmol) in ethanol (10 ml) was treated with sulfuric acid (drop), trimethoxymethane (10 ml) and refluxed for 1 hour. The resulting solution was cooled, diluted with water (100 ml), ethyl acetate (100 ml), and saturated bicarbonate (20 ml), and the layers were separated. The organic layers were washed with water and brine, then dried over magnesium sulfate, filtered, concentrated, and purified by normal phase chromatography on silica gel eluting with a gradient of ethyl acetate in hexanes to afford 500 mg of the title compound as a mixture of ethyl and methyl esters, as a colorless oil.
MS (EI) (M+H)+ 304/306 for C11H15BrNO4 (M−H)− 302/304 for C11H15BrNOt;
A solution of 2,5-dibromonicotinic acid (1 g, 3.5 mmol), 2-methoxyethanol (1.686 mL, 21.36 mmol) in DMF (10 mL) was treated with sodium hydride then warmed to 60° C. for 30 minutes. The reaction was diluted with water (100 ml), acidified (1N HCl), and extracted with ethyl acetate (3×100 ml). The combined organic layers were washed with brine, dried over magnesium sulfate, filtered, and the solvents were removed under reduced pressure. The resulting orange oil was purified by normal phase chromatography on silica gel eluting with a gradient of methanol in dichloromethane to give the title compound in solution with DMF, which was carried forward without further purification.
MS (EI) (M+H)+ 276/278 for C9H11BrNO4 (M−H)− 274/276 for C9H9BrNO4
A solution of 2-(5-bromopyridin-3-yl)-5-methyl-1,3,4-oxadiazole (Intermediate 418, 870 mg, 3.62 mmol) in dichloromethane (25 mL) was treated with 3-chlorobenzoperoxoic acid (2031 mg, 9.06 mmol) and stirred at room temperate for 16 hours. Solvents were removed under reduced pressure and the residue was purified by normal phase chromatography on silica gel, eluting with a gradient of methanol in dichloromethane to give 900 mg of the title compound as a off white solid.
MS (EI) (M+H)+ 256/258 for C8H7BrN3O2;
A mixture of 2-(5-bromopyridin-3-yl)-5-(difluoromethyl)-1,3,4-oxadiazole 2,2-difluoroacetate (Intermediate 430, 350 mg, 0.96 mmol) in ammonia (6 mL, 42.00 mmol, 7M in methanol) was heated to 130° C. for 15 min in a microwave reactor. The solvents were removed and the residue was purified by normal phase chromatography eluting with a gradient of ethyl acetate in hexanes to give 113 mg of the title compound as a white solid.
MS (EI) (M+H)+ 275/277 for C8H6BrF2N4 (M−H)− 273/275 for C8H6BrF2N4;
1H NMR (DMSO-d6) δ: 15.28 (br. s., 1H), 9.16 (d, J=1.51 Hz, 1H), 8.87 (d, J=2.07 Hz, 1H), 8.58 (s, 1H), 7.21 (d, J=53.31 Hz, 1H);
19F NMR (DMSO-d6) δ: −116.28 (br. s., 2 F);
A suspension of 5-bromonicotinohydrazide (Intermediate 433, 2 g, 9.26 mmol) in toluene (10 mL) was treated with 2,2-difluoroacetic anhydride (1.611 g, 9.26 mmol) drop wise, the resulting suspension was heated to 70° C. for 30 minutes. The reaction was cooled to room temperature and let stir for 16 hours. The solvent was removed under reduced pressure and the residue was purified by normal phase chromatography on silica gel eluting with a gradient of ethyl acetate in hexanes to give the title compound as a white solid.
MS (EI) (M+H)+ 276/278 for C8H5BrF2N3O;
1H NMR (DMSO-d6) δ: 14.22 (br. s., 1H), 9.19 (s, 1H), 9.00 (s, 1H), 8.63 (s, 1H), 7.58 (t, J=51.05 Hz, 1H), 6.28 (t, J=53.12 Hz, 1H);
19F NMR (DMSO-d6) δ: −120.83 (s, 2 F), −127.59 (s, 2 F);
Example 431 was synthesized as described for Example 429 from Intermediate 432. The product was obtained as a white solid.
MS (EI) (M+H)+ 293/295 for C8H5BrF3N4 (M−H)− 291/293 for C8H3BrF3N4;
1H NMR (DMSO-d6) δ: 15.63 (br. s., 1H), 9.17 (d, J=1.51 Hz, 1H), 8.91 (d, J=2.07 Hz, 1H), 8.61 (t, J=1.98 Hz, 1H);
19H NMR (DMSO-d6) δ: −63.79 (br. s., 3 F);
A mixture of trifluoroacetic anhydride (5 ml) and 5-bromonicotinohydrazide (Intermediate 433, 1 g, 3.24 mmol) was warmed to reflux for 5 minutes to afford an amber solution which was diluted with toluene (12 ml) and heated to reflux for an additional one hour. Solvents were removed under reduced pressure and the residue was purified by normal phase chromatography on silica gel, eluting with a gradient of dichloromethane in hexanes to afford 780 mg of the title compound as a white solid.
MS (EI) (M+H)+ 294/296 for C8H5BrF3N3O;
1H NMR (DMSO-d6) δ: 9.24 (s, 1H), 9.05 (d, J=1.32 Hz, 1H), 8.70 (s, 1H);
19F NMR (DMSO-d6) δ: −64.21 (s, 3 F);
Hydrazine (0.8 g, 24 mmol) was added to a solution of methyl 5-bromonicotinate (5.15 g, 24 mol) in toluene (10 ml) and the mixture was heated to 80° C. for 16 hours. The reaction mixture was then diluted with ethyl acetate (30 ml), cooled to RT, filtered, and the white solid that was collected was washed with ethyl acetate to give 4.64 g of the title compound as off-white solid.
MS (EI) (M+H)+ 216/218 for C6H7BrN3O (M−H)− 214/216 for C6H5BrN3O;
1H NMR (DMSO-d6) δ: 10.00 (br. s., 1H), 8.94 (d, J=1.70 Hz, 1H), 8.82 (d, J=2.26 Hz, 1H), 8.31-8.40 (m, 1H), 4.63 (br. s., 2H);
13C NMR (DMSO-d6) δ: 162.72 (s, 1 C), 152.35 (s, 1 C), 146.63 (s, 1 C), 137.02 (s, 1 C), 130.46 (s, 1 C), 120.04 (s, 1 C);
Carbontetrachloride (600 μl, 6.06 mmol) was added to a solution of N′-acetyl-2-amino-5-bromonicotinohydrazide (Intermediate 435, 270 mg, 0.99 mmol), triphenylphosphine (520 mg, 1.98 mmol), and DBU (300 μl, 1.99 mmol) in acetonitrile (50 mL). After stirring for 16 hours at RT the mixture was purified by normal phase chromatography on silica gel, eluting with a gradient of ethyl acetate in hexanes to afford 240 mg of the title compound as an off white solid.
MS (EI) (M+H)+ 255/257 for C8H8BrN4O;
1H NMR (DMSO-d6) δ: 8.27 (d, J=2.45 Hz, 1H), 8.08 (d, J=2.45 Hz, 1H), 7.45 (br. s., 2H), 2.58 (s, 3H);
HATU (2.76 g, 7.26 mmol) was added to a solution of 2-amino-5-bromonicotinic acid (1.05 g, 4.84 mmol), acetohydrazide (0.466 g, 6.29 mmol), and DIEA (1.690 mL, 9.68 mmol) in DMF (20 mL) and the resulting solution was stirred at RT for 16 hours. The reaction was then diluted with water (250 ml) and let stir at RT for 60 hrs then filtered to afford 314 mg of the title compound as a white solid.
MS (EI) (M+H)+ 273/275 for C8H10BrN4O2 (M−H)− 271/273 for C8H8BrN4O2;
1H NMR (DMSO-d6) δ: 10.30 (s, 1H), 9.89 (s, 1H), 8.20 (d, J=2.26 Hz, 1H), 8.10 (d, J=2.07 Hz, 1H), 7.22 (s, 2H), 1.91 (s, 3H);
13C NMR (DMSO-d6) δ: 168.58 (s, 1 C), 165.53 (s, 1 C), 157.38 (s, 1 C), 151.98 (s, 1 C), 138.33 (s, 1 C), 109.02 (s, 1 C), 103.80 (s, 1 C), 20.47 (s, 1 C);
Intermediate 436 was synthesized according to the procedure for Intermediate 428 from Intermediate 176.
MS (EI) (M+H)+ 256/258 for C8H7BrN3O2;
Hydrazine (2 ml) was added to a solution of (Z)-ethyl 5-iodo-6-(1-methoxyethylideneamino)nicotinate (Intermediate 437, 3 g, 8.62 mmol) in ethanol (50 mL) and warmed to 80° C. for 2 hours. Hydrochloric acid (1M in 1,4-dioxane, 1 ml) was added and heating continued for 2 hours. Additional hydrazine (2 ml) was added and heating continued for 16 hours. Solvents were removed and the crude mixture was dissolved in DMF (20 ml), treated with DIEA (3 ml), and 1,1′-carbonyl diimidazole (4 g). After stirring at RT for 8 hours, ethyl acetate (200 ml) was added and a solid was removed by filtration. The organic solution was washed with water (150 ml, then 50 ml) and brine (50 ml) then dried over magnesium sulfate. The solvents were removed under reduced pressure, and the residue was purified by normal phase chromatography on silica gel eluting with a gradient of methanol in methylene chloride. The major peak was precipitated from methylene chloride with hexanes to afford 200 mg (7.6%) of the title compound as a white powder.
MS (EI) (M+H)+ 305 for C7H61N4O2 (M−H)− 303 for C7H4IN4O2;
1H NMR (DMSO-d6) δ: 12.41 (br. s., 1H), 8.33 (d, J=2.07 Hz, 1H), 8.15 (d, J=2.07 Hz, 1H), 6.85 (d, J=0.94 Hz, 2H)
13C NMR (DMSO-d6) δ: 160.20 (s, 1 C), 154.27 (s, 1 C), 151.80 (s, 1 C), 145.55 (s, 1 C), 142.93 (s, 1 C), 10.28 (s, 1 C), 76.86 (s, 1 C)
Hydrazine (2 ml) was added to a solution of ethyl 6-amino-5-iodonicotinate (Intermediate 439, 13 g, 31.16 mmol) in 2-methoxy ethanol (50 mL) and the mixture was heated to 135° C. for three hours. Solvents were removed and trimethylorthoacetate (10 ml), HCl (1 drop), and DBU (1 ml) were added and the mixture warmed to refluxed for 2 hours. The reaction was diluted with ethyl acetate (200 ml), washed sequentially with 100 ml each of water, saturated aqueous bicarbonate, and brine then dried over magnesium sulfate. The solvents were removed under reduced pressure and the resulting material was purified by normal phase chromatography on silica gel eluting with a gradient of ethyl acetate in hexanes to give 3.1 g of the title compound as an amber oil.
MS (EI) (M+H)+ 349 for C11H14IN2O3;
1H NMR (DMSO-d6) δ: 8.80-8.83 (m, 1H), 8.56-8.60 (m, 1H), 4.32 (q, J=7.10 Hz, 2H), 3.83 (s, 3H), 1.87 (s, 3H), 1.32 (t, J=7.06 Hz, 3H)
Ethyl 6-aminonicotinate (Intermediate 440, 8.7 g, 52.35 mmol) was suspended in ethanol (150 mL), and treated sequentially with Silver (I) sulfate (16.32 g, 52.35 mmol) and then diiodine (13.29 g, 52.35 mmol). The dark suspension was warmed to 80° C. for 5 hours then additional diiodine (1.4 g) and silver sulfate (1.7 g) were added. After 2 hours, the reaction mixture was cooled to rt, and a yellow solid was removed by filtration. The filtrate was concentrated under reduced pressure, and the resulting residue was purified by normal phase chromatography eluting with a gradient of ethyl acetate in hexanes. 2.8 grams of the title compound was precipitated from a mixture of hot ethyl acetate and hexanes as an off-white solid.
MS (EI) (M+H)+ 293 for C8H10IN2O2;
1H NMR (DMSO-d6) δ: 10.31 (br. s., 2H), 8.51 (s, 1H), 8.45 (s, 1H), 4.26 (q, J=6.97 Hz, 2H), 1.28 (t, J=7.06 Hz, 3H)
13C NMR (DMSO-d6) δ: 162.90 (s, 1 C), 158.53 (s, 1 C), 148.93 (s, 1 C), 145.52 (s, 1 C), 115.80 (s, 1 C), 78.35 (s, 1 C), 60.83 (s, 1 C), 14.12 (s, 1 C).
Thionyl chloride (15 ml) was added drop wise to a refluxing suspension of 6-aminonicotinic acid (10 g, 72.40 mmol) and sulfuric acid (0.5 mL, 9.38 mmol) in ethanol (300 mL, 72.40 mmol). The suspension was heated for an additional 16 hours at which time the solution was concentrated to dryness. The material was then suspended in ethyl acetate (250 ml) and washed with sodium hydroxide (6×50 ml, 1N), until the aqueous washes were basic, then with saturated aqueous bicarbonate and brine. The organic phase was dried over magnesium sulfate, filtered, and concentrated under reduced pressure to give 8.7 g of the title compound as a white solid.
MS (EI) (M+H)+ 167 for C8H11N2O2;
1H NMR (DMSO-d6) δ: 8.49 (d, J=2.07 Hz, 1H), 7.81 (dd, J=8.67, 2.26 Hz, 1H), 6.83 (s, 2 H), 6.44 (d, J=8.67 Hz, 1H), 4.22 (q, J=7.16 Hz, 2H), 1.27 (t, J=7.16 Hz, 3H);
13C NMR (DMSO-d6) δ: 165.18 (s, 1 C), 162.48 (s, 1 C), 150.97 (s, 1 C), 137.49 (s, 1 C), 113.42 (s, 1 C), 107.01 (s, 1 C), 59.74 (s, 1 C), 14.24 (s, 1 C);
A solution of sodium nitrite (350 mg) in water (5 ml) was added dropwise to a suspension of 1-(6′-amino-5′-(5-methyl-1,3,4-oxadiazol-2-yl)-4-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridin-6-yl)-3-ethylurea (Example 258, 40 mg, 0.08 mmol) and sulfuric acid (1 ml) in water (5.00 mL) at 0° C., the mixture was allowed to warm to RT over 16 hours. The reaction was diluted with saturated aqueous sodium bicarbonate (50 ml), extracted with ethyl acetate (3×50 ml), combined organics were washed with brine, dried over magnesium sulfate, filtered, and the solvents removed under reduced pressure. The residue was purified by normal phase chromatography on silica gel eluting with a gradient of methanol in dichloromethane to afford 25 mg of the title compound crude as a tan gum which was used without further purification.
MS (EI) (M+H)+ 510 for C20H19F3N7O4S (M−H)− 508 for C20H17F3N7O4S;
Acetyl chloride (0.4 ml) was added drop wise to a solution of di-tert-butyl 2,2′-({2′-[(ethylcarbamoyl)amino]-4′-[4-(trifluoromethyl)-1,3-thiazol-2-yl]-3,3′:5′,3″-terpyridine-5,5″-diyl}dicarbonyl)dihydrazine carboxylate (Intermediate 443, 38 mg, 0.05 mmol), and stirred at RT for 18 hours, solvent was removed and the material was used in the next step without purification.
MS (EI) (M+H)+ 587 for C24H22F3N10O3S;
HATU (80 mg, 0.21 mmol) was added to a solution of 2′-[(ethylcarbamoyl)amino]-4′-[4-(trifluoromethyl)-1,3-thiazol-2-yl]-3,3′:5′,3″-terpyridine-5,5″-dicarboxylic acid (Intermediate 444, 60 mg, 0.11 mmol), tert-butyl hydrazinecarboxylate (50 mg, 0.38 mmol) and DIEA (0.2 mL, 1.15 mmol) in DMF (3 ml) and the resulting solution was stirred at RT for 20 hours. Ethyl acetate (50 ml) was added, followed by water (50 ml), and the layers were separated. The aqueous phase was extracted with ethyl acetate (3×50 m ml), and the combined organic layers were washed sequentially with saturated aqueous bicarbonate and brine, then dried over magnesium sulfate, filtered, and the solvent removed under reduced pressure. The material was purified by normal phase chromatography on silica gel eluting with a gradient of methanol in dichloromethane to afford 40 mg of the title compound as a tan solid.
MS (EI) (M+H)+ 787 for C34H38F3N10O7S (M−H)− 785 for C34H36F3N10O7S;
1H NMR (DMSO-d6) δ: 10.41 (d, J=0.75 Hz, 2H), 9.03 (d, J=8.48 Hz, 2H), 8.94 (s, 1H), 8.90 (s, 1H), 8.79 (s, 1H), 8.63 (s, 1H), 8.45 (d, J=5.84 Hz, 2H), 8.36 (d, J=0.94 Hz, 1H), 8.13 (d, J=11.30 Hz, 3H), 3.16 (d, J=5.27 Hz, 2H), 1.43 (s, 18H), 1.02-1.13 (m, 3H)
A degassed solution of 1-(3,5-dibromo-4-(4-(trifluoromethyl)thiazol-2-yl)pyridin-2-yl)-3-ethylurea (Intermediate 445, 60 mg, 0.13 mmol), ethyl 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)nicotinate (77 mg, 0.28 mmol), diphenylphospinoferocenyl palladium dichloride (10.34 mg, 0.01 mmol), and potassium carbonate (26.2 mg, 0.19 mmol) in acetonitrile (3 ml) and water (3.00 ml) under nitrogen was heated in a microwave reactor for 1 hour at 100° C. Lithium hydroxide (0.3 ml, 2N in water) was added and the solution was heated to 100° C. in a microwave reactor. The reaction was then diluted with ethyl acetate (50 ml) and water (50 ml), and the layers were separated. The aqueous phase was washed with ethyl acetate (50 ml), filtered then acidified with 1N hydrochloric acid and extracted with ethyl acetate (3×50 ml). The combined organic layers were washed with brine, dried over magnesium sulfate, filtered, and the solvents removed under reduced pressure to give 50 mg of the title compound as a pale yellow gum, which was used in the next step with no further purification.
MS (EI) (M+H)+ 559 for C24H18F3N6O5S (M−H)− 557 for C24H16F3N6O5S;
1H NMR (DMSO-d6) δ: 13.47 (br. s., 2H), 8.95 (d, J=1.88 Hz, 3H), 8.66 (d, J=2.07 Hz, 1H), 8.64 (s, 1H), 8.53 (d, J=1.88 Hz, 1H), 8.36 (s, 1H), 8.28 (s, 1H), 8.06-8.13 (m, 1H), 7.96-8.03 (m, 1H), 3.12-3.25 (m, 2H), 1.02-1.11 (m, 3H)
19F NMR (DMSO-d6) δ: −62.73 (s, 3 F)
A mixture of 1-ethyl-3-(4-(4-(trifluoromethyl)thiazol-2-yl)pyridin-2-yl)urea (from synthesis of Intermediate 12, 350 mg, 1.11 mmol) and 1-bromopyrrolidine-2,5-dione (350 mg, 1.97 mmol) in DMF (30 mL) was heated to 70° C. for 2 hours. The reaction was diluted with water (300 ml) to afford a brown precipitate which was recovered by filtration. This solid was purified by normal phase chromatography on silica gel eluting with a gradient of ethyl acetate in hexanes to give 90 mg of the title compound as a brown solid.
MS (EI) (M+H)+ 475 for C12H10Br2F3N4OS (M−H)− 473 for C12H8Br2F3N4OS;
1H NMR (DMSO-d6) δ: 8.87 (s, 1H), 8.60 (s, 1H), 8.24 (br. s., 2H), 3.23 (qd, J=6.97, 6.03 Hz, 2H), 1.11 (t, J=7.16 Hz, 3H);
19H NMR (DMSO-d6) δ: −61.99 (s, 3 F);
A solution of tert-butyl 2-(6-(6-(3-ethylureido)-4-(4-(6-methoxypyridin-2-yl)thiazol-2-yl)pyridin-3-yl)pyrazine-2-carbonyl)hydrazinecarboxylate (Intermediate 447, 30 mg, 0.05 mmol) in MeOH (20 mL), was treated with acetyl chloride (1 mL, 0.05 mmol) drop wise. After stirring at RT for 18 hours, solvents were removed under reduced pressure to give 26 mg of the title compound as a white solid, which was used without further purification.
MS (EI) (M+H)+ 492 for C22H22N9O3S (M−H) 490 for C22H20N9O3S;
HATU (50 mg, 0.13 mmol) was added to a solution of 6-(6-(3-ethylureido)-4-(4-(6-methoxypyridin-2-yl)thiazol-2-yl)pyridin-3-yl)pyrazine-2-carboxylic acid (Intermediate 486, mg, 0.05 mmol), tert-butyl hydrazinecarboxylate (30 mg, 0.23 mmol), and DIEA (50 μL, 0.29 mmol) in DMF (6 mL), and the mixture stirred at RT for 48 hours. The reaction was diluted with ethyl acetate (50 ml) and water (50 ml), and the layers were separated. The aqueous phase was extracted with ethyl acetate (3×50 ml), and the combined organic layers were washed sequentially with saturated aqueous bicarbonate and brine then dried over magnesium sulfate, filtered, and the solvents were removed under reduced pressure. The resulting residue was purified by normal phase chromatography on silica gel, eluting with a gradient of ethyl acetate in hexanes to afford 30 mg of the title compound as a white solid.
MS (EI) (M+H)+ 592 for C27H30N9O5S (M−H)− 590 for C27H28N9O5S;
1H NMR (DMSO-d6) δ: 10.53 (s, 1H), 9.60 (s, 1H), 9.08 (s, 1H), 9.03 (s, 1H), 8.76 (s, 1H), 8.69 (s, 1H), 8.40 (s, 1H), 8.23 (s, 1H), 7.85 (br. s., 1H), 7.70 (s, 1H), 7.54 (br. s., 1H), 6.76 (d, J=8.29 Hz, 1H), 3.92 (s, 3H), 3.10-3.28 (m, 2H), 1.38 (s, 9H), 1.17 (t, J=7.16 Hz, 3H).
A solution of 1-ethyl-3-(5′-(hydrazinecarbonyl)-4-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridin-6-yl)urea (Intermediate 9, 100 mg, 0.22 mmol) in pyridine (1.5 ml) was treated with 1-chloro-2-methyl-1-oxopropan-2-yl acetate (0.5 ml) and allowed to stir at RT for 30 minutes. Volatiles were removed under reduced pressure and the residue was purified by normal phase chromatography on silica gel eluting with ethyl acetate in hexanes to afford 100 mg of the title compound as an amber gum.
MS (EI) (M+H)+ 580 for C24H25F3N7O5S (M−H) 578 for C24H23F3N7O5S;
1H NMR (DMSO-d6) δ: 10.60 (s, 1H), 9.95 (s, 1H), 9.50 (s, 1H), 9.06 (d, J=1.88 Hz, 1H), 8.65 (d, J=1.88 Hz, 1H), 8.57 (s, 1H), 8.37 (s, 1H), 8.25 (s, 1H), 8.22 (s, 1H), 7.55 (t, J=5.37 Hz, 1H), 3.12-3.27 (m, 2H), 2.03 (s, 3H), 1.56 (s, 6H), 1.11 (t, J=7.16 Hz, 3H); 19F NMR (DMSO-d6) δ: −62.41 (s, 3 F);
The following Intermediates were prepared as described for Intermediate 448 using the starting materials indicated in the table.
N,N′-methanediylidenedicyclohexanamine (120 mg, 0.58 mmol) was added to a solution of 1-ethyl-3-(5′-(hydrazinecarbonyl)-4-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridin-6-yl)urea (Intermediate 9, 200 mg, 0.44 mmol), and sodium 2-chloroacetate (51.6 mg, 0.44 mmol) in 1,4-dioxane (10 mL). After stirring at RT for 16 hours the solution was warmed to 50° C. and HATU (200 mg) was added. After stirring for 1 hour, potassium carbonate (100 mg) was added and one hour later pyridine (0.5 ml) was added, and the mixture stirred at 1 hr at 50° C. The solvents were then removed under reduced pressure and the residue was purified by normal phase chromatography on silica gel eluting with a gradient of methanol in dichloromethane to give crude title compound as a pale yellow solid, which was used without further purification.
MS (EI) (M+H)+ 528 for C20H18ClF3N7O3S (M−H)− 526 for C20H18ClF3N7O3S;
1H NMR (DMSO-d6) δ: 10.80 (s, 1H), 10.50 (s, 1H), 9.51 (s, 1H), 9.05 (d, J=1.88 Hz, 1H), 8.66 (d, J=1.88 Hz, 1H), 8.57 (s, 1H), 8.38 (s, 1H), 8.24 (s, 1H), 8.21 (t, J=2.07 Hz, 1H), 7.55 (t, J=5.37 Hz, 1H), 4.21 (s, 2H), 3.05-3.27 (m, 2H), 1.11 (t, J=7.16 Hz, 3H);
19F NMR (DMSO-d6) δ: −62.43 (s, 3 F)
Di(1H-imidazol-1-yl)methanone (295 mg, 1.82 mmol) was added to a solution of 3-bromo-5-(hydrazinecarbonyl)pyridine 1-oxide (Intermediate 466, 310 mg, 1.34 mmol) in DMF (10 mL) and the mixture was stirred for 20 hours. The reaction was then diluted with ethyl acetate (100 ml), water (100 ml), and hydrochloric acid (1N, 10 ml), and the layers were separated. The aqueous phase extracted with ethyl acetate (3×100 ml), and the combined organic layers were washed with brine, dried over magnesium sulfate, and the solvents removed under reduced pressure. The resulting residue was purified by normal phase chromatography on silica gel eluting with a gradient of methanol in dichloromethane to afford 150 mg of the title compound as a pale yellow solid.
MS (EI) (M+H)+ 258/2260 for C7H5BrN3O3 (M−H)− 256/258 for C7H3BrN3O3;
1H NMR (DMSO-d6) δ: 13.02 (br. s., 1H), 8.77 (s, 1H), 8.48 (s, 1H), 7.88 (s, 1H);
Hydrazine (0.120 g, 3.75 mmol) was added to a solution of 3-bromo-5-(methoxycarbonyl)pyridine 1-oxide (Intermediate 467, 16 g, 3.75 mmol) in ethanol (50 mL), and heated to 70° C. for 19 hours, solvents were removed under reduced pressure and the residue was purified by normal phase chromatography on silica gel eluting with a gradient of methanol in dichloromethane to afford 310 mg of the title compound as a brown gummy solid.
MS (EI) (M+H)+ 232/234 for C6H7BrN3O2 (M−H)− 230/232 for C6H5BrN3O2;
1H NMR (DMSO-d6) δ: 10.11 (br. s., 1H), 8.72 (s, 1H), 8.50 (s, 1H), 7.89 (s, 1H), 4.65 (br. s., 2H);
A solution of methyl 5-bromonicotinate (1.6 g, 7.41 mmol) in dichloromethane (25 mL) was treated with 3-chlorobenzoperoxoic acid (1.992 g, 8.89 mmol) and stirred at room temperature for 16 hours. The resulting suspension was filtered, and the filtrate purified by normal phase chromatography on silica gel eluting with a gradient of ethyl acetate in hexane. The major peak was triturated from ethyl acetate with hexanes to give the title compound as a peach solid (1.4 g, 6.03 mmol, 81%).
MS (EI) (M+H)+ 232/234 for C7H7BrNO3;
1H NMR (DMSO-d6) δ: 8.85 (s, 1H), 8.51 (d, J=1.13 Hz, 1H), 7.94 (d, J=1.13 Hz, 1H), 3.89 (s, 3H);
(R)-tert-butyl 1-(5-(6′-(3-ethylureido)-4′-(4-(trifluoromethyl)thiazol-2-yl)-3,3′-bipyridin-5-yl)-1,3,4-oxadiazol-2-yl)-2-methylpropylcarbamate
Intermediate 468 was synthesized according to the procedure for Example 264 from Intermediate 461.
MS (EI) (M+H)+ 633 for C28H32F3N8O4S (M−H)− 631 for C28H30F3N8O4S;
Intermediate 469 was synthesized according to the procedure for Intermediate 268 from Intermediate 9 and (R)-2-(tert-butoxycarbonylamino)-3-methylbutanoic acid.
MS (EI) (M+H)+ 651 for C28H34F3N8O5S (M−H)− 649 for C28H32F3N8O5S;
A mixture of (1-(4-bromo-5′-(hydrazine carbonyl)-3,3′-bipyridin-6-yl)-3-ethylurea (Intermediate 471, 60 mg, 0.16 mmol), 1,1′-carbonyldiimmidazol (34.4 mg, 0.21 mmol) and diisopropyl ethylamine (0.041 ml, 0.24 mmol) in DMF (3 ml) was heated at 50° C. for 4 hours, cooled down to room temperature. The crude was concentrated and purified by column chromatography on silica gel (5% methanol in dichloromethane) to give the desired product as a solid (62 mg).
MS (ESP) 407.2 (MH) for C15H13BrN6O3.
1H-NMR (DMSO-d6) δ: 1.09 (t, 3H); 3.19 (t, 2H); 7.48 (t, 1H); 8.04 (s, 1H); 8.23 (t, 1H); 8.29 (s, 1H); 8.80 (d, 1H); 9.0 (d, 1H); 9.45 (s, 1H).
Ethyl 4′-bromo-6′-(3-ethylureido)-3,3′-bipyridine-5-carboxylate (Intermediate 472, 1.32 g, 2.85 mmol), hydrazine hydrate (1.416 ml, 28.53 mmol) were mixed in ethanol (20 ml), heated at 80° C. for 2 d, cooled down to room temperature. The crude was diluted with ethyl acetate; the resulting precipitate was filtered and washed with ethyl acetate, collected as the desired product (920 mg).
MS (ESP) 381.06 (MH+) for C14H15BrN6O2
1H-NMR (DMSO-d6): 1.08 (t, 3H); 3.17 (q, 2H); 3.58 (br, 2H); 7.43 (t, 1H); 8.05 (s, 1H); 8.27 (s, 2H); 8.85 (s, 1H); 9.03 (s, 1H); 9.43 (s, 1H); 11.15 (br, 1H).
1-(4-Bromo-5-iodopyridin-2-yl)-3-ethylurea (Intermediate 473, 1.33 g, 3.59 mmol), ethyl 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)nicotinate (1.049 g, 3.59 mmol), paladium-tetrakistriphenylphosphine (0.415 g, 0.36 mmol) and K2CO3 (0.745 g, 5.39 mmol) were suspended in a mixture of DMF (10 ml) and water (1.000 ml). The suspension was degassed and purged with nitrogen then heated at 100° C. for 1.5 h. The reaction mixture was cooled down to room temperature and filtered; the filtrate was concentrated and purified by column chromatography on silica gel to give the desired product (1.32 g).
MS (ESP) 395.02 (MH+) for C16H17BrN4O3.
1H-NMR (CDCl3): 1.29 (t, 3H); 1.45 (t, 3H); 3.45 (q, 2H); 4.47 (q, 2H); 7.30 (br, 1H); 8.12 (s, 1H); 8.38 (t, 1H); 8.84 (2s, 2×H); 9.29 (s, 1H).
4-bromo-5-iodopyridin-2-amine (Intermediate 474, 3.2 g, 10.71 mmol) was dissolved in dry chloroform (15 mL). Isocyanatoethane (2.52 mL, 32.12 mmol) was added and the reaction mixture was refluxed for 24 hrs. The reaction was cooled down to room temperature and hexanes was added. The resulting precipitate was collected by filtration to give the desired product (3.14 g).
MS (ESP+) 371.99 (MH+) for C8H9BrIN3O.
1H-NMR (DMSO-d6): 1.06 (t, 3H); 3.32 (q, 2H); 7.24 (br, 1H); 8.05 (s, 1H); 8.52 (s, 1H); 9.31 (s, 1H).
4-Bromopyridin-2-amine (2.5 g, 14.45 mmol) was dissolved in DMF (6 mL)/CHCl3 (20 mL), 1-iodopyrrolidine-2,5-dione (6.50 g, 28.90 mmol) was added, and the mixture was stirred at 45° C. for 2 days. CHCl3 was evaporated and the remaining solution was poured into water (15 ml) and extracted with EtOAc (15 ml×3). The organic phase was concentrated and purified by ISCO eluted with Hex/EtOAc (gradient) to give the title compound (3.2 g).
MS (ESP) 298.88 (MH+) for C5H4BrIN2.
1H-NMR (DMSO-d6): 4.51 (br, 2H); 6.80 (s, 1H); 8.35 (s, 1H).
1-ethyl-3-(5′-(5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)-4-((trimethylsilyl)ethynyl)-3,3′-bipyridin-6-yl)urea (Intermediate 476, 84 mg, 0.20 mmol) was suspended in methanol (5 ml), and NaOH (2 ml, 2.00 mmol) was added. The mixture was stirred at room temperature for 2 hrs, aqueous HCl solution (2N) was added to adjust the ph to 6.5. DCM (10 ml) was added and the organic layer was washed with brine and dried over MgSO4, and concentrated to a volume of 2 ml. Hexanses was added and the resulting precipitate was filtered and washed with DCM, collected as the desired product (25 mg).
MS (ESP) 351 (MH+) for C17H14N6O3
1H-NMR (DMSO-d6): 1.10 (t, 3H); 3.20 (m, 2H); 4.66 (s, 1H); 7.61 (m, 1H); 7.78 (s, 1H); 8.34 (m, 1H); 8.41 (s, 1H); 8.92 (d, 1H); 8.98 (d, 1H); 9.43 (s, 1H); 12.84 (br, 1H) ppm
1-(4-bromo-5′-(5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)-3,3′-bipyridin-6-yl)-3-ethylurea (Intermediate 470, 400 mg, 0.99 mmol), ethynyltrimethylsilane (116 mg, 1.18 mmol), copper(I) iodide (18.80 mg, 0.10 mmol), Et3N (0.550 mL, 3.95 mmol), and Pd(PPh3)4 (57.1 mg, 0.05 mmol) were combined in anhydrouse DMF (10 mL) and heated at 80° C. for 4 hours. After cooling down to room temperature, the crude sample was filtered through celite and the filtrate was concentrated and purified by column chromatography on silica gel (Hex/EtOAc) to give the tile compound (160 mg).
MS (ESP) 423 (MH+) for C20H22N6O3Si
1H-NMR (DMSO-d6): 0.12 (s, 9H); 1.10 (t, 3H); 3.20 (m, 2H); 7.57 (m, 1H); 7.72 (s, 1H); 8.41 (m, 1H); 8.45 (s, 1H); 8.92 (d, 1H); 8.99 (d, 1H); 9.41 (s, 1H); 12.86 (s, 1H) ppm
(6-(3-Ethylureido)-5′-(5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)-3,3′-bipyridin-4-yl)methyl methanesulfonate (Intermediate 478, 350 mg, 0.81 mmol), sodium azide (52.4 mg, 0.81 mmol) were mixed in DMF (4 ml), stirred at 60° C. for 2 hr, diluted with dichloromethane, the solvent was evaporated and the residue was mixed with silica gel and dry loaded onto isco column (silica gel), eluted with 10% MeOH in dichloromethane to give the title product as a white solid (206 mg).
MS (ESP) 382 (MH+) for C16H15N9O3
1H-NMR (DMSO-d6): 1.10 (t, 3H); 3.20 (m, 2H); 4.55 (s, 2H); 7.69 (s, 1H); 7.81 (t, 1H); 8.18 (m, 2H); 8.77 (d, 1H); 9.00 (d, 1H); 9.40 (s, 1H); 12.84 (s, 1H) ppm
1-Ethyl-3-(4-(hydroxymethyl)-5′-(5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)-3,3′-bipyridin-6-yl)urea (Intermediate 479, 420 mg, 1.18 mmol), methane sulfonyl chloride (0.137 ml, 1.77 mmol) were mixed in DMF (4 ml)/DCM (15 ml) and stirred at 25° C. for 2 hr. The reaction mixture was then diluted with DCM (10 ml), washed with brine and the organic phase was concentrated and diluted in dichloromethane. Hexanses was added and the resulting precipitate was filtered and collected as the desired product (350 mg).
MS (ESP) 435 (MH+) for C17H18N6O6S
1-Ethyl-3-(5′-(hydrazine carbonyl)-4-(hydroxymethyl)-3,3′-bipyridin-6-yl)urea (Intermediate 480, 470 mg, 1.42 mmol), CDI (476 mg, 2.85 mmol) and DIEA (0.497 ml, 2.85 mmol) were suspended in DMF (5 ml) and stirred at room temperature for 12 hours. The reaction mixture turned into solution, and sodium hydroxide (aqueous solution, 2N, 1 ml) was added, and the reaction was stirred for 30 min. Hydrogen chloride (aqueous, 2N, ˜1 ml) was added, and the mixture was extracted with 10% methanol in dichloromethane (10 ml×5). The organic layer was dried over anhydrous MgSO4, filtered and concentrated to volume of ˜3 ml, ether (10 ml) was added, the resulting precipitates was filtered and washed with ether and DCM, collected to give the title compound (425 mg).
MS (ESP) 357 (MH+) for C16H16N6O4
1H-NMR (DMSO-d6): 1.10 (t, 3H); 3.19 (m, 2H); 4.41 (s, 2H); 5.47 (m, 1H); 7.65 (s, 1H); 8.10 (s, 1H); 8.18 (m, 2H); 8.70 (br, 1H); 8.95 (d, 1H); 9.36 (s, 1H); 12.84 (s, 1H) ppm
Ethyl 6′-(3-ethylureido)-4′-(hydroxymethyl)-3,3′-bipyridine-5-carboxylate (Intermediate 481, 500 mg, 1.45 mmol), hydrazine hydrate (0.721 ml, 14.52 mmol) were mixed in ethanol (10 ml), heated at 80° C. for 25 hr., cooled down to room temperature, ethyl acetate was added and the resulting solid was filtered and washed with ethyl acetate, to give the desired product (440 mg).
MS (ESP) 331 (MH+) for C15H18N6O3
In a round bottom flask, 1-(5-bromo-4-(hydroxymethyl)pyridin-2-yl)-3-ethylurea (Intermediate 482, 5.26 g, 19.19 mmol), ethyl 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)nicotinate (5.60 g, 19.19 mmol), Pd(PPh3)4 (2.217 g, 1.92 mmol) and cesium carbonate (12.50 g, 38.38 mmol) were suspended in a 4:1 mixture of 1,4 dioxane/water. The suspension was degassed and purged with nitrogen then heated in the microwave at 100° C. for 2 hours. The reaction was cooled to room temperature. Diluted with DCM (20 ml)/MeOH (5 ml) and washed with brine. The organic phase was dried and concentrated then purified by column chromatography on silica gel eluted with DCM/MeOH (95/5%) to give the title compound as a solid. (3.5 g)
MS (ESP) 345 (MH+) for C17H20N4O4
1H-NMR (DMSO-d6): 1.27 (t, 3H); 1.45 (t, 3H); 3.43 (m, 2H); 4.46 (q, 2H); 4.65 (s, 2H); 8.02 (br, 1H); 8.30 (br, 2H); 8.77 (s, 1H); 9.28 (s, 1H).
Methyl 5-bromo-2-(3-ethylureido) isonicotinate (Intermediate 483, 5 g, 15.82 mmol), NaBH4 (1.795 g, 47.45 mmol) were mixed in EtOH (20 ml), and the mixture was refluxed for over night. The solvent was evaporated and the residue was mixed with DCM (50 ml). A 2N HCl aqueous solution was added (10 ml), and the mixture was stirred for 10 min, then the saturated NaHCO3 was added and the mixture was extracted with DCM (20 ml×3), the organic layer was dried over MgSO4, filtered and the volume was reduced to 10 ml. The precipitate that formed was filtered and collected as the desired product (2.34 g).
MS (ESP) 275 (MH+) for C9H12BrN3O2
1H-NMR (CD3OD): 1.20 (t, J=7.33 Hz, 3H); 4.59 (s, 2H); 7.35 (s, 1H); 8.22 (s, 1H) ppm.
To a solution of methyl 2-amino-5-bromoisonicotinate (25 g, 108.20 mmol) in chloroform (20 mL) was added ethyl isocyanate (17.00 mL, 216.41 mmol), and the reaction mixture heated to reflux for 16 h then cooled to ambient temperature. The product was precipitated with hexane (200 mL), filtered, washed with hexane (2×50 mL) and dried to give 27.5 g light yellow color solid as the desired product.
MS (ESP): 304.00 (M+2) for C10H12BrN3O3
1H NMR (DMSO-d6): 1.07 (t, J=7.20 Hz, 3H); 3.01-3.25 (m, 2H); 3.91 (s, 3H); 7.17 (t, J=5.31 Hz, 1H); 8.02 (d, J=1.52 Hz, 1H); 8.46 (s, 1H); 9.41 (s, 1H)
A solution of tetrahydro-2H-pyran-4-yl 5-bromo-6-(tetrahydro-2H-pyran-4-yloxy)nicotinate (Intermediate 281, 2 g) and hydrazine (2 mL) in ethanol (20 mL) was heated to reflux for 20 h. The reaction mixture was cooled to room temperature and concentrated under reduced pressure. The crude product and 1,1,1-trimethoxyethane (20 ml, 166.46 mmol) was heated reflux and treated with concentrated aqueous HCl (drop), the resulting clear colorless solution was refluxed for 20 minutes, treated with DBU (0.2 ml, 1.33 mmol) and refluxed an additional 20 min. The material was concentrated under reduced pressure to give a tan gum which was purified by flash chromatography on silica gel eluting with a gradient of ethyl acetate in hexanes to give the title compound as a white solid (1.77 g)
MS (EI) (M+H)+ 340/342 for C13H14BrN3O3;
Di(1H-imidazol-1-yl)methanone (290 mg, 1.82 mmol) was added to a solution of 3-bromo-5-(hydrazinecarbonyl)pyridine (Intermediate 433, 300 mg, 1.34 mmol) in DMF (10 mL) and the reaction was allowed to proceed for 20 hours. The reaction was then diluted with ethyl acetate (100 ml), water (100 ml), and hydrochloric acid (1N, 10 ml), and the layers were separated. The aqueous phase extracted with ethyl acetate (3×100 ml), and the combined organics were washed with brine, dried over magnesium sulfate, filtered and the solvents were removed under reduced pressure. The resulting residue was purified by normal phase chromatography on silica gel eluting with a gradient of methanol in dichloromethane to afford 150 mg of the title compound as a pale yellow solid.
MS (EI) (M+H)+ 242/250 for C7H5BrN3O2;
A mixture of 6-(3-ethylureido)-4-(4-(6-methoxypyridin-2-yl)thiazol-2-yl)pyridin-3-ylboronic acid (Intermediate 415, 700 mg, 0.88 mmol), 6-chloropyrazine-2-carboxylic acid (278 mg, 1.75 mmol), cesium carbonate (571 mg, 1.75 mmol), dipalladium tridibenzilidine acetone (40.1 mg, 0.04 mmol), Dicyclohexyl TriisopropylBiphenyl phosphine (84 mg, 0.18 mmol), in 1,4-dioxane (12 mL) and water (3.0 mL) was degassed, then heated in a microwave reactor at 110° C. for 1 hr. The reaction was diluted with ethyl acetate (25 ml), and the resulting solid was removed by filtration, the solid was washed with ethyl acetate, ethyl acetate/methanol, and 1N sodium hydroxide. The combined filtrates were extracted with 1N sodium hydroxide (3×50 ml). The combined aqueous extracts were acidified (con. HCl), and the aqueous phase was extracted with ethyl acetate (3×50 ml). The combined organics were washed with brine, dried over magnesium sulfate, filtered, and the solvent was removed under reduced pressure. The resulting solid was washed exhaustively with methanol solutions in methylene chloride to afford 30 mg of the title compound as a beige solid.
MS (EI) (M+H)+ 478 for C25H20N7O4S (M−H)− 476 for C25H18N7O4S;
1H NMR (DMSO-d6) δ: 9.62 (s, 1H), 9.13 (s, 1H), 8.85 (s, 1H), 8.49 (s, 1H), 8.36 (s, 1H), 8.28 (s, 1H), 7.70 (t, J=7.82 Hz, 1H), 7.63 (br. s., 1H), 6.96 (d, J=7.35 Hz, 1H), 6.76 (d, J=8.29 Hz, 1H), 3.91 (s, 3H), 3.13-3.28 (m, 2H), 1.12 (t, J=7.25 Hz, 3H)
This application claims priority to U.S. 61/031,621 filed Feb. 26, 2008, the entire teachings of which are incorporated herein by reference.
Number | Date | Country | |
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61031621 | Feb 2008 | US |