Patent Application
20240109853
The present invention relates to compounds that are inhibitors of alpha protein kinase 1 (ALPK1) and related compositions and methods.
Alpha-kinases display little sequence similarity to conventional protein kinases. A total of six alpha kinase members have been identified. These include alpha-protein kinase 1 (ALPK1), ALPK2, ALPK3, elongated factor-2 kinase (eEF2K), and transient receptor potential cation channel M6 and M7 (TRPM6 and TRPM7). See Ryazanov et al., Curr Biol 9:R43-45 (1999) and Ryazanov et al., Proc Natl Acad Sci USA 94:4884-4889 (1997).
ALPK1 is an intracytoplasmic serine threonine protein kinase that plays an important role in activating the innate immune response to bacteria via TRAF-interacting protein with forkhead-associated domain (TIFA) dependent proinflammatory nuclear factor-kappa-B (NFkB) signaling. See Zimmermann et al. Cell Rep. 20:2384-2395 (2017); Milivojevic et al., PLoS Pathog. 13:E1006224-E1006224 (2017); and Zhou et al., Nature 561:122-126 (2018).
Inappropriate activation of ALPK1 signaling has been implicated in diseases and disorders associated with excessive or inappropriate inflammation. For example, ALPK1 has been implicated in monosodium urate monohydrate (MSU)-induced inflammation and gout. Lee et al., Sci. Rep. 6:25740-25740(2016). Elevated ALPK1 expression has also been associated with lymph node metastasis and tumor growth in oral squamous cell carcinoma. Chen et al., Am J Pathol 189:190-199 (2019). In addition, genetic mutations in ALPK1 have been associated with spiroandenoma, spiroandenocarcinoma, “Retinal dystrophy, Optic nerve edema, Splenomegaly, Anhidrosis and migraine Headache” (“ROSAH”) syndrome, and “Periodic Fever, Aphthous Stomatitis, Pharyngitis, and Adenitis” (“PFAPA”) syndrome. See e.g., Rashid et al., Nature Communications (2019); Williams et al., Genetics in Medicine 21:2103-2115 (2019); and Sangiorgi et al. Eur. J. Human Genetics (2019).
The disclosure provides compounds of Formula I and subembodiments of Formula I described herein, that are inhibitors of ALPK1 kinase activity, and related compositions and methods.
In some aspects, provided herein are compounds of Formula I
wherein A, p, R1, R2, R3, R4 and R5 are as defined herein
In some embodiments, compounds of Formula I are represented by Formula IA
wherein p, R1, R2, R3, R4, R5, R6, and R9 are as defined herein.
In some embodiments, compounds of Formula I are represented by Formula IA-1
wherein p, R1, R2, R3, R4, R5, R6, and R9 are as defined herein.
In some embodiments, compounds of Formula I are represented by Formula IB
wherein p, R2, R3, R4, R5, R13, D, E, F, and G are as defined herein.
In some embodiments, compounds of Formula I are represented by Formula IB-1
Wherein p, R2, R3, R4, R5, R15, R16, and R17 are as defined herein.
In some embodiments, compounds of Formula I are represented by Formula IC
Wherein p, m, R2, R3, R4, R5, R18 are as defined herein.
In some aspects, provided herein are compounds of Formula XI,
wherein X, A, p, R1, R2, R3, R4 and R5 are as defined herein.
In some embodiments, compounds of Formula I are represented by Formula XI-A,
wherein X, p, R1, R2, R3, R4, R5, R6, and R9 are as defined herein.
In some embodiments, compounds of Formula I are represented by Formula XI-A-1,
wherein X, p, R1, R2, R3, R4, R5, R6, and R9 are as defined herein.
In some embodiments, compounds of Formula I are represented by Formula XI-A-1-a,
wherein p, R1, R2, R3, R4, R5, R6, and R9 are as defined herein.
In some embodiments, compounds of Formula I are represented by Formula XI-B,
wherein X, p, R2, R3, R4, R5, R13, D, E, F, and G are as defined herein.
In some embodiments, compounds of Formula I are represented by Formula XI-B-1,
wherein X, p, R2, R3, R4, R5, R15, R16, and R17 are as defined herein.
In some embodiments, compounds of Formula I are represented by Formula XI-B-1-a,
wherein p, R2, R3, R4, R5, R15, R16, and R7 are as defined herein.
In some embodiments, compounds of Formula I are represented by Formula XI-C,
wherein X, p, m, R2, R3, R4, R5, R18 are as defined herein.
In some embodiments, compounds of Formula XI are represented by Formula XI-C-1,
wherein p, m, R2, R3, R4, R5, R18 are as defined herein.
In embodiments, the disclosure provides a pharmaceutical composition comprising a compound of Formula I, IA, IB, IC, XI, XI-A, XI-B, or XI-C, or a subembodiment thereof, as described herein.
In embodiments, the disclosure provides a method for inhibiting ALPK1 kinase activity in a cell or tissue of a subject in need of such therapy, the method comprising administering to the subject a compound of Formula I, IA, IB, IC, XI, XI-A, XI-B, or XI-C, or a subembodiment thereof, as described herein.
In embodiments, the disclosure provides a method for inhibiting or reducing inflammation in a target tissue of a subject in need of such treatment, the method comprising administering to the subject a compound of Formula I, IA, IB, IC, XI, XI-A, XI-B, or XI-C, or a subembodiment thereof, as described herein.
In embodiments, the disclosure provides a method for treating a disease, disorder, or condition characterized by excessive or inappropriate ALPK1-dependent proinflammatory signaling in a subject in need of such therapy, the method comprising administering to the subject a compound of Formula I, IA, IB, IC, XI, XI-A, XI-B, or XI-C, or a subembodiment thereof, as described herein.
In embodiments, the disease, disorder, or condition is selected from sepsis, cancer, spiroandenoma, spiroandenocarcinoma, “Retinal dystrophy, Optic nerve edema, Splenomegaly, Anhidrosis and migraine Headache” (“ROSAH”) syndrome, and “Periodic Fever, Aphthous Stomatitis, Pharyngitis, and Adenitis” (“PFAPA”) syndrome.
In embodiments, the cancer is selected from lung cancer, colon cancer, and oral squamous cancer.
In embodiments, the disease or disorder is selected from ROSAH and PFAPA.
In embodiments, the disease or disorder is sepsis.
In embodiments, the disease or disorder is spiradenoma or spiroandenocarcinoma.
In embodiments, the subject in need of such therapy or treatment is a subject carrying one or more genetic mutations in ALPK1. In embodiments, at least one mutation is an activating mutation.
The disclosure provides compounds that are inhibitors of ALPK1, compositions comprising same, and methods for their use in therapy.
The term “ALPK1” is used herein to refer interchangeably to isoform 1 (Q96QP1-1) or the alternative splice variant isoform 2 (Q96QP1-2) of the human sequence identified by UniProtKB—Q96QP1 (ALPK1_HUMAN).
As used herein, the term “alkyl” refers to a straight or branched, saturated, aliphatic radical having the number of carbon atoms indicated. Alkyl can include any number of carbons, such as C1-2, C1-3, C1-4, C1-5, C1-6, C1-7, C1-8, C1-9, C1-10, C2-3, C2-4, C2-5, C2-6, C3-4, C3-5, C3-6, C4-5, C4-6 and C5-6. For example, C1-6 alkyl includes, but is not limited to, methyl, ethyl, propyl, isopropyl, butyl, isobutyl, sec-butyl, tert-butyl, pentyl, isopentyl, hexyl, etc. Alkyl can also refer to alkyl groups having up to 20 carbons atoms, such as, but not limited to heptyl, octyl, nonyl, decyl, etc. Alkyl groups can be substituted or unsubstituted.
As used herein, “alkenyl” refers to a straight chain or branched hydrocarbon having at least 2 carbon atoms and at least one double bond. Alkenyl can include any number of carbons, such as C2, C2-3, C2-4, C2-5, C2-6, C2-7, C2-8, C2-9, C2-10, C3, C3-4, C3-5, C3-6, C4, C4-5, C4-6, C5, C5-6, and C6. Alkenyl groups can have any suitable number of double bonds, including, but not limited to, 1, 2, 3, 4, 5 or more. In some embodiments, an alkenyl group has 1 double bond. Alkenyl groups can be substituted or unsubstituted.
As used herein, “alkynyl” refers to a straight chain or branched hydrocarbon having at least 2 carbon atoms and at least one triple bond. Alkenyl can include any number of carbons, such as C2, C2-3, C2-4, C2-5, C2-6, C2-7, C2-8, C2-9, C2-10, C3, C3-4, C3-5, C3-6, C4, C4-5, C4-6, C5, C5-6, and C6. Alkynyl groups can have any suitable number of triple bonds, including, but not limited to, 1, 2, 3, 4, 5 or more. In some embodiments, an alkynyl group has 1 triple bond. Alkynyl groups can be substituted or unsubstituted.
As used herein, the term “alkylene” refers to a straight or branched, saturated, aliphatic radical having the number of carbon atoms indicated, and linking at least two other groups, i.e., a divalent hydrocarbon radical. The two moieties linked to the alkylene can be linked to the same atom or different atoms of the alkylene group. For instance, a straight chain alkylene can be the bivalent radical of —(CH2)n-, where n is 1, 2, 3, 4, 5 or 6. Representative alkylene groups include, but are not limited to, methylene, ethylene, propylene, isopropylene, butylene, isobutylene, sec-butylene, pentylene and hexylene. Alkylene groups can be substituted or unsubstituted. In some embodiments, alkylene groups are substituted with 1-2 substituents. As a non-limiting example, suitable substituents include halogen and hydroxyl.
As used herein, the term “alkoxy” or “alkoxyl” refers to an alkyl group having an oxygen atom that connects the alkyl group to the point of attachment: alkyl-O—. As for alkyl group, alkoxyl groups can have any suitable number of carbon atoms, such as C1-6. Alkoxyl groups include, for example, methoxy, ethoxy, propoxy, iso-propoxy, butoxy, 2-butoxy, iso-butoxy, sec-butoxy, tert-butoxy, pentoxy, hexoxy, etc. The alkoxy groups can be substituted or unsubstituted.
As used herein, the term “alkenyloxy” or “alkenyloxyl” refers to an alkenyl group, as defined above, having an oxygen atom that connects the alkenyl group to the point of attachment: alkenyl-O—. Alkenyloxyl groups can have any suitable number of carbon atoms, such as C1-6. Alkenyloxyl groups can be further substituted with a variety of substituents described within. Alkenyloxyl groups can be substituted or unsubstituted.
“Aminoalkyl” means a linear monovalent hydrocarbon radical of one to six carbon atoms or a branched monovalent hydrocarbon radical of three to six carbons substituted with —NR′R″ where R′ and R″ are independently hydrogen, alkyl, haloalkyl, or hydroxyalkyl, each as defined herein, e.g., aminomethyl, aminoethyl, methylaminomethyl, and the like.
As used herein, the term “halogen” or “halo” refers to fluorine, chlorine, bromine and iodine.
As used herein, the term “haloalkyl” refers to alkyl, as defined above, where some or all of the hydrogen atoms are replaced with halogen atoms. As for alkyl group, haloalkyl groups can have any suitable number of carbon atoms, such as C1-6. For example, haloalkyl includes trifluoromethyl, fluoromethyl, etc.
As used herein, the term “haloalkoxyl” or “haloalkoxy” refers to an alkoxyl group where some or all of the hydrogen atoms are substituted with halogen atoms. As for an alkyl group, haloalkoxy groups can have any suitable number of carbon atoms, such as C1-6. The alkoxy groups can be substituted with 1, 2, 3, or more halogens.
As used herein, the term “deuteroalkyl” means an alkyl radical as defined above wherein one to six hydrogen atoms in the alkyl radical are replaced by deuterium, e.g., —CH2D, —CHD2, —CD3, —CH2CD3, and the like.
As used herein, the term “hydroxyalkyl” refers to an alkyl radical wherein at least one of the hydrogen atoms of the alkyl radical is replaced by OH. Examples of hydroxyalkyl include, but are not limited to, hydroxy-methyl, 2-hydroxy-ethyl, 2-hydroxy-propyl, 3-hydroxy-propyl and 4-hydroxy-butyl.
As used herein, the term “oxo” refers to an oxygen atom connected to the point of attachment by a double bond (═O).
As used herein, the term “aryl” refers to an aromatic ring system having any suitable number of ring atoms and any suitable number of rings. Aryl groups can include any suitable number of ring atoms, such as, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15 or 16 ring atoms, as well as from 6 to 10, 6 to 12, or 6 to 14 ring members. Aryl groups can be monocyclic, fused to form bicyclic or tricyclic groups, or linked by a bond to form a biaryl group. Representative aryl groups include phenyl, naphthyl and biphenyl. Other aryl groups include benzyl, having a methylene linking group. Some aryl groups have from 6 to 12 ring members, such as phenyl, naphthyl or biphenyl. Other aryl groups have from 6 to 10 ring members, such as phenyl or naphthyl. Some other aryl groups have 6 ring members, such as phenyl. Aryl groups can be substituted or unsubstituted.
As used herein, the term “heteroaryl” refers to a monocyclic or fused bicyclic aromatic ring assembly containing 5 to 12 ring atoms, where from 1 to 5 of the ring atoms are a heteroatom such as N, O or S. Additional heteroatoms can also be useful, including, but not limited to, B, Al, Si and P. The heteroatoms can also be oxidized, such as, but not limited to, —S(O)— and —S(O)2—. Heteroaryl groups can include any number of ring atoms, such as, 3 to 6, 4 to 6, 5 to 6, 3 to 8, 4 to 8, 5 to 8, 6 to 8, 3 to 9, 3 to 10, 3 to 11, or 3 to 12 ring members. Any suitable number of heteroatoms can be included in the heteroaryl groups, such as 1, 2, 3, 4, or 5, or 1 to 2, 1 to 3, 1 to 4, 1 to 5, 2 to 3, 2 to 4, 2 to 5, 3 to 4, or 3 to 5. Heteroaryl groups can have from 5 to 9 ring members and from 1 to 4 heteroatoms, or from 5 to 9 ring members and from 1 to 3 heteroatoms, or from 5 to 6 ring members and from 1 to 4 heteroatoms, or from 5 to 6 ring members and from 1 to 3 heteroatoms. The heteroaryl group can include groups such as pyrrole, pyridine, imidazole, pyrazole, triazole, tetrazole, pyrazine, pyrimidine, pyridazine, triazine (1,2,3-, 1,2,4- and 1,3,5-isomers), purine. The heteroaryl groups can also be fused to aromatic ring systems, such as a phenyl ring, to form members including, but not limited to, benzopyrroles such as indole and isoindole, benzopyridines such as quinoline and isoquinoline, benzopyrazine (quinoxaline), benzopyrimidine (quinazoline), benzopyridazines such as phthalazine and cinnoline, benzothiophene, and benzofuran. Other heteroaryl groups include heteroaryl rings linked by a bond, such as bipyridine. Heteroaryl groups can be substituted or unsubstituted.
As used herein, “cycloalkyl” refers to a saturated ring assembly containing from 3 to 10 ring atoms, or the number of atoms indicated. Cycloalkyl can include any number of carbons, such as C3-6, C4-6, C5-6, C3-8, C4-8, C5-8, C6-8. Cycloalkyl rings can be saturated or unsaturated, when unsaturated cycloalkyl rings can have one or two double bonds. Cycloalkyl rings include, for example, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, and cyclooctyl. Cycloalkyl groups can be substituted or unsubstituted.
As used herein, the term“heterocyclyl” or“heterocyclic” refers to a heterocyclic group that is saturated or partially saturated and is a monocyclic or a polycyclic ring; which has 3 to 16, most preferably 5 to 10 and most preferably 1 or 4 ring atoms; wherein one or more, preferably one to four, especially one or two ring atoms are a heteroatom selected from oxygen, nitrogen and sulfur (the remaining ring atoms therefore being carbon). The term heterocyclyl excludes heteroaryl. The heterocyclic group can be attached to the rest of the molecule through a heteroatom, selected from oxygen, nitrogen and sulfur, or a carbon atom. The heterocyclyl can include fused or bridged rings as well as spirocyclic rings. Examples of heterocyclyl include dihydrofuranyl, dioxolanyl, dioxanyl, dithianyl, piperazinyl, pyrrolidine, dihydropyranyl, oxathiolanyl, dithiolane, oxathianyl, thiomorpholino, oxiranyl, aziridinyl, oxetanyl, oxepanyl, azetidinyl, tetrahydrofuranyl, tetrahydrothiophenyl, pyrrolidinyl, tetrahydropyranyl, piperidinyl, morpholino, piperazinyl, azepinyl, oxapinyl, oxaazepanyl, oxathianyl, thiepanyl, azepanyl, dioxepanyl, and diazepanyl.
As used herein, “spiroheterocyclyl” refers to a specific bicyclic heterocyclic group wherein the 2 ring systems are connected through a single carbon atom. For example, the term“spiroheterocyclyl” can refer to a 6-10 spiro heterocyclyl. Examples of include, but not limited to, 6,9-diazaspiro[4.5]decane, 2-oxa-6,9-diazaspiro[4.5]decane, 2-Oxa-6-azaspiro[3.4]octane, 6-azaspiro[3.4]octane, 2,6-diazaspiro[3.4]octane, 1,6-diazaspiro[3.4]octane, 2,8-diazaspiro[4.5]decane,2,7-diazaspiro[4.4]nonane, 1-thia-8-azaspiro[4.5]decane 1,1-dioxide, I-oxa-7-azaspiro[4.4]nonane and 1-oxa-9-azaspiro[5.5]undecane.
As used herein, “bridged heterocyclyl” refers to a C3_cycloalkyl ring or a 3- to 6-membered heterocyclyl ring, as defined above, where two non-adjacent ring vertices (“bridgehead atoms”) of the cycloalkyl ring or the heterocyclyl ring are linked to form an additional cyclic moiety (a “bridge”). The bridge comprises 1 to 4 ring vertices, not including the bridgehead atoms. Examples include, but not limited to, 2,5-diazabicyclo[2.2.1]heptane, 3,6-diazabicyclo[3.1.1]heptane, 3,8-diazabicyclo[3.2.1]octane, 2,5-diazabicyclo[2.2.2]octane, 3,9-diazabicyclo[3.3.1]nonane, 2-thia-5-azabicyclo[2.2.1]heptane 2,2-dioxide, 2-azabicyclo[2.2.1]hept-5-ene, 3-oxa-8-azabicyclo[3.2.1]octane, 3-oxa-6-azabicyclo[3.1.1]heptane, 6-oxa-3-azabicyclo[3.1.1]heptane and 2-oxa-5-azabicyclo[2.2.1]heptane.
The term “bicyclic heterocyclyl” refers to a heterocyclic group as defined above where the two ring systems are connected through two adjacent ring vertices (e.g., a fused ring system). Typical “bicyclic heterocyclyl” rings include 6 to 11 ring members having 1 to 4 heteroatom ring vertices selected from N, O, and S (the remaining ring atoms therefore being carbon). Examples include, but not limited to, benzodioxolyl, benzimidazolyl, benzisoxazolyl, benzofurazanyl, benzopyranyl, benzothiopyranyl, benzofuryl, benzothiazolyl, benzothienyl, benzotriazolyl, benzoxazolyl, chromanyl, cinnolinyl, dihydrobenzofuryl, dihydroisobenzofuranyl, dihydrobenzothienyl, dihydrobenzothiopyranyl, dihydrobenzothiopyranyl sulfone, indolinyl, indolyl, isochromanyl, isoindolinyl, isoquinolinyl, isothiazolidinyl, naphthyridinyl, pyrazolopyridinyl, quinazolinyl, quinolinyl, quinoxalinyl, tetrahydroisoquinolinyl, tetrahydroquinolinyl.
As used herein, “saturated or unsaturated” refers to a cyclic system where two of the atoms in the group may be bound to one another by a single bond, a double bond, or a triple bond. Saturated moieties are those having only single bonds, where moieties having multiple bonds (e.g., at least one double bond or at least one triple bondare referred to as unsaturated.
When needed, any definition herein may be used in combination with any other definition to describe a composite structural group. By convention, the trailing element of any such definition is that which attaches to the parent moiety. For example, the composite group cycloalkoxyl means that a cycloalkyl group is attached to the parent molecule through an oxyl group.
The term “pharmaceutically acceptable salts” is meant to include salts of the active compounds which are prepared with relatively nontoxic acids or bases, depending on the particular substituents found on the compounds described herein. When compounds of the present invention contain relatively acidic functionalities, base addition salts can be obtained by contacting the neutral form of such compounds with a sufficient amount of the desired base, either neat or in a suitable inert solvent. Examples of salts derived from pharmaceutically-acceptable inorganic bases include aluminum, ammonium, calcium, copper, ferric, ferrous, lithium, magnesium, manganic, manganous, potassium, sodium, zinc and the like. Salts derived from pharmaceutically-acceptable organic bases include salts of primary, secondary and tertiary amines, including substituted amines, cyclic amines, naturally-occurring amines and the like, such as arginine, betaine, caffeine, choline, N,N′-dibenzylethylenediamine, diethylamine, 2-diethylaminoethanol, 2-dimethylaminoethanol, ethanolamine, ethylenediamine, N-ethylmorpholine, N-ethylpiperidine, glucamine, glucosamine, histidine, hydrabamine, isopropylamine, lysine, methylglucamine, morpholine, piperazine, piperidine, polyamine resins, procaine, purines, theobromine, triethylamine, trimethylamine, tripropylamine, tromethamine and the like. When compounds of the present invention contain relatively basic functionalities, acid addition salts can be obtained by contacting the neutral form of such compounds with a sufficient amount of the desired acid, either neat or in a suitable inert solvent. Examples of pharmaceutically acceptable acid addition salts include those derived from inorganic acids like hydrochloric, hydrobromic, nitric, carbonic, monohydrogencarbonic, phosphoric, monohydrogenphosphoric, dihydrogenphosphoric, sulfuric, monohydrogensulfuric, hydriodic, or phosphorous acids and the like, as well as the salts derived from relatively nontoxic organic acids like acetic, propionic, isobutyric, malonic, benzoic, succinic, suberic, fumaric, mandelic, phthalic, benzenesulfonic, p-tolylsulfonic, citric, tartaric, methanesulfonic, and the like. Also included are salts of amino acids such as arginate and the like, and salts of organic acids like glucuronic or galactunoric acids and the like (see, for example, Berge, S. M., et al, “Pharmaceutical Salts”, Journal of Pharmaceutical Science, 1977, 66, 1-19). Certain specific compounds of the present invention contain both basic and acidic functionalities that allow the compounds to be converted into either base or acid addition salts.
The neutral forms of the compounds may be regenerated by contacting the salt with a base or acid and isolating the parent compound in the conventional manner. The parent form of the compound differs from the various salt forms in certain physical properties, such as solubility in polar solvents, but otherwise the salts are equivalent to the parent form of the compound for the purposes of the present disclosure.
Certain compounds of the present invention possess asymmetric carbon atoms (optical centers) or double bonds; the racemates, diastereomer, geometric isomers, regioisomers and individual isomers (e.g., separate enantiomers) are all intended to be encompassed within the scope of the present invention. In some embodiments, the compounds of the present invention are a particular enantiomer, anomer, or diastereomer substantially free of other for ms.
As used herein, the term “substantially free” refers to an amount of 10% or less of another isomeric form, preferably 8%, 5%, 4%, 3%, 2%, 1%, 0.5%, or less of another form. In some embodiments, the isomer is a stereoisomer.
The disclosure provides compounds represented by formula (I) and pharmaceutically acceptable salts thereof:
The present invention discloses novel heterocyclic compounds as inhibitors of ALPK1. The compounds are represented by formula I
In some embodiments, A in Formula I is a bond.
In some embodiments, A in Formula I is azetidinyl.
In some embodiments, A in Formula I is —O—.
In some embodiments, A in Formula I is —N(R6)—.
In some embodiments, A in Formula I is —CH2—N(R6)—.
In some embodiments, A in Formula I is —CHR9—N(R6)—.
In some embodiments, the compound of formula I is represented by the compound of formula IA, formula IA-1, formula IA-2 and/or a stereoisomer, a stable isotope, or a pharmaceutically acceptable salt thereof
Wherein p, R1, R2, R3, R4, R5, R6, and R9 are as defined above.
In some embodiments R6 in formula I, IA, IA-1, or IA-2 is H, C1-C6 alkyl or C1-C6 hydroxyalkyl.
In some embodiments R9 in formula I and IA is CH3 or CH2OH.
In some embodiments R9 in formula I and IA is saturated C3-C6 cycloalkyl.
In some embodiments R′ in formula I, IA, IA-1, or IA-2 is selected from H and optionally substituted C1-C6 alkyl, wherein
In some embodiments R′ in formula I, IA, IA-1, or IA-2 is optionally substituted saturated or unsaturated C3-C6 cycloalkyl, wherein
In some embodiments R′ in formula I, IA, IA-1, or IA-2 combines with R6 to form a 3-6 membered heterocycloalkyl substituted with 0-3 moieties independently selected from the group consisting of halo, —OH,—COOH, —NH2, ═O, —CN, C1-C6 alkyl, C1-C6 alkenyl, C1-C6 hydroxyalkyl, C1-C6 haloalkyl, C1-C6 aminoalkyl, and C1-C6 alkoxyl.
In some embodiments R′ in formula I, IA, IA-1, or IA-2 is C1-C6 alkyl substituted with 0-4 substituents independently selected from —OH, C1-C6 hydroxyalkyl, C1-C6 alkoxyl, —OC(O)(R7a), —S(O)2N(R7aR7b) and —N(R7aR8a), wherein
In some embodiments R′ in formula I, IA, IA-1, or IA-2 is C1-C6 alkyl substituted with 0-2 substituents independently selected from —OH, C1-C6 hydroxyalkyl, and —S(O)2N(R7aR8a), wherein each R7a and R8a are independently selected from H, and C1-C6 alkyl.
In some embodiments R1 in formula I, IA, IA-1, or IA-2 is optionally substituted C1-C6 hydroxyalkyl.
In some embodiments R1 in formula I, IA, IA-1, or IA-2 is a 5-10 membered heteroaryl containing 1-4 heteroatom ring vertices selected from N, O, and S,
In some embodiments R1 in formula I, IA, IA-1, or IA-2 is pyridiyl substituted with 0 to 3 moieties selected from halo, —OH,—COOH, —NH2, —CN, C1-C6 alkyl, C1-C6 alkenyl, 3-7 membered heterocyclyl containing 1-2 heteroatom ring vertices selected from N, O, and S, wherein
In some embodiments R1 in formula I, IA, IA-1, or IA-2 is a saturated or unsaturated 7-8 membered bridged heterocyclyl containing 1-2 heteroatom ring vertices selected from N, O, and S, wherein
In some embodiments R1 in formula I, IA, IA-1, or IA-2 is a saturated or unsaturated 7-11 membered spiroheterocyclyl containing 1-2 heteroatom ring vertices selected from N, O, and S, wherein
In some embodiments, R1 in formula I, IA, IA-1, or IA-2 is aryl substituted with 0-3 substituents selected from halo, a 3-7 membered heterocyclyl containing 1-2 heteroatom ring vertices selected from N, O, and S; a 7-8 membered bridged heterocyclyl containing 1-2 heteroatom ring vertices selected from N, O, and S; and a saturated or unsaturated 7-11 membered spiroheterocyclyl containing 1-2 heteroatom ring vertices selected from N, O, and S, wherein
In some embodiments R1 in formula I, IA, IA-1, or IA-2 is aryl substituted with 0-3 moieties selected from halo —OH,—COOH, —NH2, ═O, —CN, C1-C6 alkyl, C1-C6 alkenyl, C1-C6 hydroxyalkyl, C1-C6 haloalkyl, C1-C6 aminoalkyl, C1-C6 alkoxyl, and a 3-7 membered heterocyclyl containing 1-2 heteroatom ring vertices selected from N, O, and S,
In some embodiments R1 in formula I, IA, IA-1, or IA-2 is aryl substituted with 0-3 moieties selected from halo and a 3-7 membered heterocyclyl containing 1-2 heteroatom ring vertices selected from N, O, and S, wherein
In some embodiments, the compound of formula I is represented by the compound of Formula IB and/or a stereoisomer, a stable isotope, or a pharmaceutically acceptable salt thereof
In some embodiments, D, E, F and G in Formula IB are CR10, CR14, CR12, and CR11, respectively.
In some embodiments, F and G in Formula IB are CR14 and CR11, respectively, E is N or CR14 and D is N or CR10.
In some embodiments, R10 and R11 in Formula IB are each H, R12 and R14 are each independently selected from halo, —OH, —COOH, —NH2, ═O, —CN, C1-C6 alkyl, C1-C6 alkenyl, C1-C6 hydroxyalkyl, C1-C6 haloalkyl, C1-C6 aminoalkyl, C1-C6 alkoxyl, saturated or unsaturated C3-C6 cycloalkyl, saturated or unsaturated C3-C6 cycloalkoxyl, —CHR7bR8b, —OR7b, —OC(O)(R7b), —C(O)(R7b), —C(O)N(R7bR8b), —C(O)O(R7b), —S(O)2N(R7bR8b) and —N(R7bR8b), wherein R7b and R8b are each independently selected from H, C1-C6 alkyl, C1-C6 alkenyl, C1-C6 hydroxyalkyl, C1-C6 haloalkyl, C1-C6 aminoalkyl, C1-C6 alkoxyl, saturated or unsaturated C3-C6 cycloalkyl, and saturated or unsaturated C3-C6 cycloalkoxyl; R13 is 3-7 membered heterocyclyl containing 1-2 heteroatom ring vertices selected from N, O, and S, saturated or unsaturated 7-8 membered bridged heterocyclyl containing 1-2 heteroatom ring vertices selected from N, O, and S, saturated or unsaturated 7-11 membered spiroheterocyclyl containing 1-2 heteroatom ring vertices selected from N, O, and S, wherein the 3-7 membered heterocyclyl, the 7-8 membered bridged heterocyclyl, and the 7-11 membered spiroheterocyclyl are optionally substituted with 0-2 moieties independently selected from halo, —OH, —COOH, —NH2, ═O, —CN, C1-C6 alkyl, C1-C6 alkenyl, C1-C6 hydroxyalkyl, C1-C6 haloalkyl, C1-C6 aminoalkyl, C1-C6 alkoxyl, saturated or unsaturated C3-C6 cycloalkyl, saturated or unsaturated C3-C6 cycloalkoxyl.
In some embodiments, R12 and R14 in Formula IB are H, R10 and R11 are each independently selected from halo, —OH, —COOH, —NH2, ═O, —CN, C1-C6 alkyl, C1-C6 alkenyl, C1-C6 hydroxyalkyl, C1-C6 haloalkyl, C1-C6 aminoalkyl, C1-C6 alkoxyl, saturated or unsaturated C3-C6 cycloalkyl, saturated or unsaturated C3-C6 cycloalkoxyl, —CHR7bR8b, —OR7b, —OC(O)(R7b), —C(O)(R7b), —C(O)N(R7bR8b), —C(O)O(R7b), —S(O)2N(R7bR8b) and —N(R7bR8b), wherein R7b and R8b are each independently selected from H, C1-C6 alkyl, C1-C6 alkenyl, C1-C6 hydroxyalkyl, C1-C6 haloalkyl, C1-C6 aminoalkyl, C1-C6 alkoxyl, saturated or unsaturated C3-C6 cycloalkyl, and saturated or unsaturated C3-C6 cycloalkoxyl; R13 is 3-7 membered heterocyclyl containing 1-2 heteroatom ring vertices selected from N, O, and S, saturated or unsaturated 7-8 membered bridged heterocyclyl containing 1-2 heteroatom ring vertices selected from N, O, and S, saturated or unsaturated 7-11 membered spiroheterocyclyl containing 1-2 heteroatom ring vertices selected from N, O, and S, wherein the 3-7 membered heterocyclyl, the 7-8 membered bridged heterocyclyl, and the 7-11 membered spiroheterocyclyl are optionally substituted with 0-2 moieties independently selected from halo, —OH, —COOH, —NH2, ═O, —CN, C1-C6 alkyl, C1-C6 alkenyl, C1-C6 hydroxyalkyl, C1-C6 haloalkyl, C1-C6 aminoalkyl, C1-C6 alkoxyl, saturated or unsaturated C3-C6 cycloalkyl, saturated or unsaturated C3-C6 cycloalkoxyl.
In some embodiments, R10, R11, R12 and R14 in Formula IB are all H; R13 is saturated or unsaturated C3-C6 cycloalkyl, 3-7 membered heterocyclyl containing 1-2 heteroatom ring vertices selected from N, O, and S, saturated or unsaturated 7-8 membered bridged heterocyclyl containing 1-2 heteroatom ring vertices selected from N, O, and S, saturated or unsaturated 7-11 membered spiroheterocyclyl containing 1-2 heteroatom ring vertices selected from N, O, and S, wherein the 3-7 membered heterocyclyl, the 7-8 membered bridged heterocyclyl, and the 7-11 membered spiroheterocyclyl are optionally substituted with 0-2 moieties independently selected from halo, —OH, —COOH, —NH2, ═O, —CN, C1-C6 alkyl, C1-C6 alkenyl, C1-C6 hydroxyalkyl, C1-C6 haloalkyl, C1-C6 aminoalkyl, C1-C6 alkoxyl, saturated or unsaturated C3-C6 cycloalkyl, saturated or unsaturated C3-C6 cycloalkoxyl.
In some embodiments, R10, R11, R12 and R14 in Formula IB are each H; R13 is 3-7 membered heterocyclyl containing 1-2 heteroatom ring vertices selected from N, O, and S w substituted with 0-2 moieties independently selected from halo, —OH, —COOH, —NH2, ═O, —CN, C1-C6 alkyl, C1-C6 alkenyl, C1-C6 hydroxyalkyl, C1-C6 haloalkyl, C1-C6 aminoalkyl, C1—C6 alkoxyl, saturated or unsaturated C3-C6 cycloalkyl, and saturated or unsaturated C3-C6 cycloalkoxyl.
In some embodiments, R10, R11, R12 and R14 in Formula IB are each H; R13 is optionally substituted saturated or unsaturated 7-8 membered bridged heterocyclyl containing 1-2 heteroatom ring vertices selected from N, O, and S substituted with 0-2 substituents selected from —OH,—COOH, —NH2, ═O, —CN, and-C1-C6 alkyl.
In some embodiments, the compound of formula IB is represented by the compound of formula IB-1 or IB-2, and/or a stereoisomer, a stable isotope, or a pharmaceutically acceptable salt thereof
In some embodiments, R15 in formula IB-1 or IB-2 is selected from C1-C6 alkyl, C1-C6 alkenyl, C1-C6 hydroxyalkyl, C1-C6 haloalkyl, C1-C6 aminoalkyl, C1-C6 alkoxyl, C1-C6 haloalkoxyl; saturated or unsaturated C3-C6 cycloalkyl, saturated or unsaturated C3-C6 cycloalkoxyl, —CHR7bR8b, wherein
In some embodiments, R15 in formula IB-1 or IB-2 is C1-C6 alkyl.
In some embodiments, both R2 and R3 in formula IB-1 or IB-2 are methyl groups.
In some embodiments, R2 and R3 in formula IB-1 or IB-2 are each independently a methyl or an ethynyl group.
In some embodiments, IB-1 is represented by Formula IB-1-a, or Formula IB-2-a
or a pharmaceutically acceptable salt thereof.
In some embodiments, IB-1 is represented by Formula IB-1-b, or Formula IB-2-b
or a pharmaceutically acceptable salt thereof, wherein R4 is halo.
In some embodiments, IB-1 is represented by Formula (IB-1-c), or Formula IB-2-c
or a pharmaceutically acceptable salt thereof.
In some embodiments, R5 in formula IB-1 or IB-2 is H or methyl.
The present invention discloses novel heterocyclic compounds as inhibitors of ALPK1. The compounds are represented by formula IC
In some embodiments, R18 in formula IC is H.
The present invention also discloses novel heterocyclic compounds as inhibitors of ALPK1. The compounds are represented by formula XI,
In some embodiments, X in Formula XI is S.
In some embodiments, X in Formula XI is O.
In some embodiments, X in Formula XI is NH.
In some embodiments, A in Formula XI is a bond.
In some embodiments, A in Formula XI is azetidinyl.
In some embodiments, A in Formula XI is —O—.
In some embodiments, A in Formula XI is —N(R6)—.
In some embodiments, A in Formula XI is —CH2—N(R6)—.
In some embodiments, A in Formula XI I is —CHR9—N(R6)—.
In some embodiments, the compound of formula I is represented by the compound of formula XI-A, formula XI-A-1, formula XI-A-2 and/or a stereoisomer, a stable isotope, or a pharmaceutically acceptable salt thereof.
In some embodiments, the compound of formula XI is represented by the compound of formula XI-A-1-a, and/or a stereoisomer, a stable isotope, or a pharmaceutically acceptable salt thereof
X, p, R1, R2, R3, R4, R5, R6, and R9 are as defined above.
In some embodiments X in formula XI, XI-A, XI-A-1, XI-A-2, or XI-A-1-a is S, O or NH.
In some embodiments R6 in formula XI, XI-A, XI-A-1, XI-A-2, or XI-A-1-a is H, C1-C6 alkyl or C1-C6 hydroxyalkyl.
In some embodiments R9 in formula XI and XI-A is CH3 or CH2OH.
In some embodiments R9 in formula XI and XI-A is saturated C3-C6 cycloalkyl.
In some embodiments R1 in formula XI, XI-A, XI-A-1, XI-A-2, or XI-A-1-a is selected from H and optionally substituted C1-C6 alkyl, wherein
In some embodiments R1 in formula XI, XI-A, XI-A-1, XI-A-2, or XI-A-1-a is optionally substituted saturated or unsaturated C3-C6 cycloalkyl, wherein
In some embodiments R1 in formula XI, XI-A, XI-A-1, XI-A-2, or XI-A-1-a combines with R6 to form a 3-6 membered heterocycloalkyl substituted with 0-3 moieties independently selected from the group consisting of halo, —OH,—COOH, —NH2, ═O, —CN, C1-C6 alkyl, C1-C6 alkenyl, C1-C6 hydroxyalkyl, C1-C6 haloalkyl, C1-C6 aminoalkyl, and C1-C6 alkoxyl.
In some embodiments R1 in formula XI, XI-A, XI-A-1, XI-A-2, or XI-A-1-a is C1-C6alkyl substituted with 0-4 substituents independently selected from —OH, C1-C6 hydroxyalkyl, C1-C6 alkoxyl, —OC(O)(R7a), —S(O)2N(R7aR8a) and —N(R7aR8a), wherein
In some embodiments R1 in formula XI, XI-A, XI-A-1, XI-A-2, or XI-A-1-a is C1-C6alkyl substituted with 0-2 substituents independently selected from —OH, C1-C6 hydroxyalkyl, and —S(O)2N(R7aR8a), wherein each R7a and R8a are independently selected from H, and C1-C6 alkyl.
In some embodiments R1 in formula XI, XI-A, XI-A-1, XI-A-2, or XI-A-1-a is optionally substituted C1-C6 hydroxyalkyl.
In some embodiments R1 in formula XI, XI-A, XI-A-1, XI-A-2, or XI-A-1-a is a 5-10 membered heteroaryl containing 1-4 heteroatom ring vertices selected from N, O, and S,
In some embodiments R1 in formula XI, XI-A, XI-A-1, XI-A-2, or XI-A-1-a is pyridiyl substituted with 0 to 3 moieties selected from halo, —OH,—COOH, —NH2, —CN, C1-C6 alkyl, C1-C6 alkenyl, 3-7 membered heterocyclyl containing 1-2 heteroatom ring vertices selected from N, O, and S, wherein
In some embodiments R1 in formula XI, XI-A, XI-A-1, XI-A-2, or XI-A-1-a is a saturated or unsaturated 7-8 membered bridged heterocyclyl containing 1-2 heteroatom ring vertices selected from N, O, and S, wherein
In some embodiments R1 in formula XI, XI-A, XI-A-1, XI-A-2, or XI-A-1-a is a saturated or unsaturated 7-11 membered spiroheterocyclyl containing 1-2 heteroatom ring vertices selected from N, O, and S, wherein
In some embodiments, R1 in formula XI, XI-A, XI-A-1, XI-A-2, or XI-A-1-a is aryl substituted with 0-3 substituents selected from halo, a 3-7 membered heterocyclyl containing 1-2 heteroatom ring vertices selected from N, O, and S; a 7-8 membered bridged heterocyclyl containing 1-2 heteroatom ring vertices selected from N, O, and S; and a saturated or unsaturated 7-11 membered spiroheterocyclyl containing 1-2 heteroatom ring vertices selected from N, O, and S, wherein
In some embodiments R1 in formula XI, XI-A, XI-A-1, XI-A-2, or XI-A-1-a is aryl substituted with 0-3 moieties selected from halo —OH,—COOH, —NH2, ═O, —CN, C1-C6 alkyl, C1-C6 alkenyl, C1-C6 hydroxyalkyl, C1-C6 haloalkyl, C1-C6 aminoalkyl, C1-C6 alkoxyl, and a 3-7 membered heterocyclyl containing 1-2 heteroatom ring vertices selected from N, O, and S,
In some embodiments R1 in formula XI, XI-A, XI-A-1, XI-A-2, or XI-A-1-a is aryl substituted with 0-3 moieties selected from halo and a 3-7 membered heterocyclyl containing 1-2 heteroatom ring vertices selected from N, O, and S, wherein
In some embodiments, the compound of formula XI is represented by the compound of Formula XI-B and/or a stereoisomer, a stable isotope, or a pharmaceutically acceptable salt thereof,
In some embodiments, D, E, F and G in Formula XI-B are CR10, CR14, CR12, and CR11, respectively.
In some embodiments, F and G in Formula XI-B are CR14 and CR11, respectively, E is N or CR14 and D is N or CR11.
In some embodiments, R10 and R11 in Formula XI-B are each H, R12 and R14 are each independently selected from halo, —OH, —COOH, —NH2, ═O, —CN, C1-C6 alkyl, C1-C6 alkenyl, C1-C6 hydroxyalkyl, C1-C6 haloalkyl, C1-C6 aminoalkyl, C1-C6 alkoxyl, saturated or unsaturated C3-C6 cycloalkyl, saturated or unsaturated C3-C6 cycloalkoxyl, —CHR7bR8b, —OR7b, —OC(O)(R7b), —C(O)(R7b), —C(O)N(R7bR8b), —C(O)O(R7b), —S(O)2N(R7bR8b) and —N(R7bR8b), wherein R7b and R8b are each independently selected from H, C1-C6 alkyl, C1-C6 alkenyl, C1-C6 hydroxyalkyl, C1-C6 haloalkyl, C1-C6 aminoalkyl, C1-C6 alkoxyl, saturated or unsaturated C3-C6 cycloalkyl, and saturated or unsaturated C3-C6 cycloalkoxyl; R13 is 3-7 membered heterocyclyl containing 1-2 heteroatom ring vertices selected from N, O, and S, saturated or unsaturated 7-8 membered bridged heterocyclyl containing 1-2 heteroatom ring vertices selected from N, O, and S, saturated or unsaturated 7-11 membered spiroheterocyclyl containing 1-2 heteroatom ring vertices selected from N, O, and S, wherein the 3-7 membered heterocyclyl, the 7-8 membered bridged heterocyclyl, and the 7-11 membered spiroheterocyclyl are optionally substituted with 0-2 moieties independently selected from halo, —OH, —COOH, —NH2, ═O, —CN, C1-C6 alkyl, C1-C6 alkenyl, C1-C6 hydroxyalkyl, C1-C6 haloalkyl, C1-C6 aminoalkyl, C1-C6 alkoxyl, saturated or unsaturated C3-C6 cycloalkyl, saturated or unsaturated C3-C6 cycloalkoxyl.
In some embodiments, R12 and R14 in Formula XI-B are H, R10 and R11 are each independently selected from halo, —OH, —COOH, —NH2, ═O, —CN, C1-C6 alkyl, C1-C6 alkenyl, C1-C6 hydroxyalkyl, C1-C6 haloalkyl, C1-C6 aminoalkyl, C1-C6 alkoxyl, saturated or unsaturated C3-C6 cycloalkyl, saturated or unsaturated C3-C6 cycloalkoxyl, —CHR7bR8b, —OR7, —OC(O)(R7b), —C(O)(R7b), —C(O)N(R7bR8b), —C(O)O(R7b), —S(O)2N(R7bR8b) and —N(R7bR8b), wherein R7b and R8b are each independently selected from H, C1-C6 alkyl, C1-C6 alkenyl, C1-C6 hydroxyalkyl, C1-C6 haloalkyl, C1-C6 aminoalkyl, C1-C6 alkoxyl, saturated or unsaturated C3-C6 cycloalkyl, and saturated or unsaturated C3-C6 cycloalkoxyl; R3 is 3-7 membered heterocyclyl containing 1-2 heteroatom ring vertices selected from N, O, and S, saturated or unsaturated 7-8 membered bridged heterocyclyl containing 1-2 heteroatom ring vertices selected from N, O, and S, saturated or unsaturated 7-11 membered spiroheterocyclyl containing 1-2 heteroatom ring vertices selected from N, O, and S, wherein the 3-7 membered heterocyclyl, the 7-8 membered bridged heterocyclyl, and the 7-11 membered spiroheterocyclyl are optionally substituted with 0-2 moieties independently selected from halo, —OH, —COOH, —NH2, ═O, —CN, C1-C6 alkyl, C1-C6 alkenyl, C1-C6 hydroxyalkyl, C1-C6 haloalkyl, C1-C6 aminoalkyl, C1-C6 alkoxyl, saturated or unsaturated C3-C6 cycloalkyl, saturated or unsaturated C3-C6 cycloalkoxyl.
In some embodiments, R10, R11, R12 and R14 in Formula XI-B are all H; R13 is saturated or unsaturated C3-C6 cycloalkyl, 3-7 membered heterocyclyl containing 1-2 heteroatom ring vertices selected from N, O, and S, saturated or unsaturated 7-8 membered bridged heterocyclyl containing 1-2 heteroatom ring vertices selected from N, O, and S, saturated or unsaturated 7-11 membered spiroheterocyclyl containing 1-2 heteroatom ring vertices selected from N, O, and S, wherein the 3-7 membered heterocyclyl, the 7-8 membered bridged heterocyclyl, and the 7-11 membered spiroheterocyclyl are optionally substituted with 0-2 moieties independently selected from halo, —OH, —COOH, —NH2, ═O, —CN, C1-C6 alkyl, C1-C6 alkenyl, C1-C6 hydroxyalkyl, C1-C6 haloalkyl, C1-C6 aminoalkyl, C1-C6 alkoxyl, saturated or unsaturated C3-C6 cycloalkyl, saturated or unsaturated C3-C6 cycloalkoxyl.
In some embodiments, R10, R11, R12 and R14 in Formula XI-B are each H; R13 is 3-7 membered heterocyclyl containing 1-2 heteroatom ring vertices selected from N, O, and S w substituted with 0-2 moieties independently selected from halo, —OH, —COOH, —NH2, ═O, —CN, C1-C6 alkyl, C1-C6 alkenyl, C1-C6 hydroxyalkyl, C1-C6 haloalkyl, C1-C6 aminoalkyl, C1-C6 alkoxyl, saturated or unsaturated C3-C6 cycloalkyl, and saturated or unsaturated C3-C6 cycloalkoxyl.
In some embodiments, R10, R11, R12 and R14 in Formula XI-B are each H; R13 is optionally substituted saturated or unsaturated 7-8 membered bridged heterocyclyl containing 1-2 heteroatom ring vertices selected from N, O, and S substituted with 0-2 substituents selected from —OH,—COOH, —NH2, ═O, —CN, and-C1-C6 alkyl.
In some embodiments, the compound of Formula XI-B is represented by the compound of Formula XI-B-1 or XI-B-2, and/or a stereoisomer, a stable isotope, or a pharmaceutically acceptable salt thereof
In some embodiments, the compound of Formula XI-B-1 or XI-B-2 is represented by the compound of formula XI-B-1-a, XI-B-2-a and/or a stereoisomer, a stable isotope, or a pharmaceutically acceptable salt thereof,
In some embodiments, R5 in Formula XI-B-1 or XI-B-2 is selected from C1-C6 alkyl, C1-C6 alkenyl, C1-C6 hydroxyalkyl, C1-C6 haloalkyl, C1-C6 aminoalkyl, C1-C6 alkoxyl, C1-C6 haloalkoxyl; saturated or unsaturated C3-C6 cycloalkyl, saturated or unsaturated C3-C6 cycloalkoxyl, —CHR7bR8b, wherein
In some embodiments, R15 in formula XI-B-1 or XI-B-2 is C1-C6 alkyl.
In some embodiments, both R2 and R3 in formula XI-B-1 or XI-B-2 are methyl groups.
In some embodiments, R2 and R3 in formula XI-B-1 or XI-B-2 are each independently a methyl or an ethynyl group.
In some embodiments, XI-B-1-a is represented by Formula XI-B-1-a-I, and XI-B-2-a is represented by Formula XI-B-2-a-I
or a pharmaceutically acceptable salt thereof, wherein R4 is halo.
In some embodiments, XI-B-1-a is represented by Formula XI-B-1-a-II, and XI-B-2-a is represented by Formula XI-B-2-a-II
or a pharmaceutically acceptable sat thereof.
In some embodiments, XI-B-1-a is represented by Formula XI-B-1-a-III, and XI-B-2-a is represented by Formula XI-B-2-a-III
or a pharmaceutically acceptable salt thereof.
In some embodiments, XI-B-1-a is represented by Formula XI-B-1-a-IV, and XI-B-2-a is represented by Formula XI-B-2-a-IV
or a pharmaceutically acceptable salt thereof.
In some embodiments, R5 in formula XI-B-1 or XI-B-2 is H or methyl.
The present invention discloses novel heterocyclic compounds as inhibitors of ALPK1. The compounds are represented by formula XI-C
Wherein X, R2, R3, R4 and R5 are as defined above formula XI; and
m is an integer from 0-6;
In some embodiments, the compound of formula XI-C is represented by the compound of formula XI-C-1, and/or a stereoisomer, a stable isotope, or a pharmaceutically acceptable salt thereof,
In some embodiments, m in formula XI-C or XI-C-1 is 1.
In some embodiments, R18 in formula XI-C or XI-C-1 is H.
In some embodiments, R2 and R3 in each of the formulas described herein are both C1-C6 alkyl groups;
In some embodiments, R2 is methyl and R3 is CH2OMe in each of the formulas described herein.
In some embodiments, R2 and R3 are each methyl in each of the formulas described herein.
In some embodiments, R2 is methyl and R3 is ethynyl in each of the formulas described herein.
In some embodiments, R2 is methyl and R3 is C3-C6 cycloalkyl.
In some embodiments, R2 is methyl, and R3 is phenyl.
In some embodiments, in each of the formulas described herein, the subscript p is 1, and R4 is attached to the phenyl ring as shown below:
wherein the wavy line represents the point of attachment to the remainder of the formula.
In some embodiments, in each of the formulas described herein, the subscript p is 1, and R4 is halo attached to the phen 1 ring as shown below:
wherein the wavy line represents the point of attachment to the remainder of the formula.
In some embodiments, in each of the formulas described herein, the subscript p is 1, and R4 is chloro attached to the phenyl ring as shown below:
wherein the wavy line represents the point of attachment to the remainder of the formula.
In some embodiments, in each of the formulas described herein, the subscript p is 1, and R4 is methoxy attached to the phenyl ring as shown below:
wherein the wavy line represents the point of attachment to the remainder of the formula.
In some embodiments, R5 in each of the formulas described herein is H.
In some embodiments, R5 in each of the formulas described herein is deuterium.
In some embodiments, R5 in each of the formulas described herein is C1-C6 deuteroalkyl. In some embodiments, R5 in each of the formulas described herein is selected from the group consisting of —CH2D, —CHD2, and —CD3.
In some embodiments, the carbon atom attached to R2 and R3 in each of the formulas described herein is chiral. In such embodiments, it is understood that R2 and R3 are not the same. In some embodiments, the carbon atom attached to R2 and R3 in each of the formulas described herein is the S isomer, referring to the absolute stereochemistry at this carbon atom. In some embodiments, the carbon atom attached to R2 and R3 in each of the formulas described herein is the R isomer, referring to the absolute stereochemistry at this carbon atom. In some embodiments, R2 is methyl and R3 is ethynyl. In some embodiments, R2 is methyl and R3 is C3-C6 cycloalkyl. In some embodiments, R2 is methyl, and R3 is phenyl. In some embodiments, R3 is methyl and R2 is ethynyl. In some embodiments, R3 is methyl and R2 is C3-C6 cycloalkyl. In some embodiments, R3 is methyl, and R2 is phenyl.
In some embodiments, the compound of Formula I is selected from
In some embodiments, the compound of Formula I is selected from
In some embodiments, the compound is selected from the examples provided herein.
NMR: Measurements were performed on a Bruker Ultrashield™ 400 (400 MHz) spectrometer using or not tetramethylsilane (TMS) as an internal standard. Chemical shifts (6) are reported ppm downfield from TMS, spectra splitting pattern are designated as single (s), doublet (d), triplet (t), quartet (q), multiplet, unresolved or overlapping signals (m), broad signal (br). Deuterated solvent are given in parentheses and have a chemical shifts of dimethyl sulfoxide (δ2.50 ppm), chloroform (δ 7.26 ppm), methanol (δ3.31 ppm), or other solvent as indicated in NMR spectral data.
Flash Column Chromatography System
HPLC Separation Conditions
SFC Chiral Separation Conditions
All starting materials, building blocks, reagents, acids, bases, dehydrating agents, solvents, and catalysts utilized to synthesis the compounds of the present invention are either commercially available or can be produced by organic synthesis methods known to one of ordinary skill in the art.
Below is the abbreviation table for chemistry:
Appropriately substituted compound M1 wherein R are suitable 1-3 groups like halo or C1-C6 alkyl, etc, and R1 and R2 are suitable groups like independently selected from H, C1-C6 alkyl and C2-C6 alkynyl, converted to acid chloride with SOCl2 or (COCl)2 under heating or room temperature. Weinreb amide was formed by the reaction of N,O-dimethylhydroxylamine hydrochloride with the acid chloride at 0° C. Grignard reagent in THF was added to the Weinreb amide at 0° C. to give the ketone, which was converted to M5 by bromination. The cyclization with thiourea under basic condition gave the intermediate M6.
Step 1. Preparation of compound 2-(4-bromophenyl)-2-methylpropanoyl chloride
Compound 2-(4-bromophenyl)-2-methylpropanoic acid (100 g, 411 mmol, 1.0 eq) in SOCl2 (175 mL, 6 eq) was warmed to reflux for 2 h. Then the solution was cooled to RT, the mixture was concentrated under reduced pressure to get dry acid chloride (yellow oil) which was used in next step without further purification.
Step 2. Preparation of compound 2-(4-bromophenyl)-N-methoxy-N,2-dimethylpropanamide
The solution of compound N,O-dimethylhydroxylamine HCl salt (48.2 g, 49 mmol, 1.2 eq) in DCM (300 mL) was cooled to 0° C. Then to the mixture was added crude acid chloride obtained from step 1 above (1.0 eq) in DCM (200 mL) and TEA (114 mL, 2 eq), and the mixture was stirred at RT overnight. The reaction mixture was quenched with H2O (200 mL). The mixture was extracted with DCM (200 mL×3), the combined organic layers were washed with water (200 mL×3), brine (200 mL×3), dried over Na2SO4, filtered and concentrated to give a residue. The desired compound (108 g, pure) was obtained as a pale yellow oil which was used in next step without further purification.
1H NMR (400 MHz, CDCl3) δ 7.42 (d, J=8.8 Hz, 2H), 7.12 (d, J=8.8 Hz, 2H), 3.08 (s, 3H), 2.71 (s, 3H), 1.49 (s, 6H).
Step 3. Preparation of compound 3-(4-bromophenyl)-3-methylbutan-2-one
The solution of compound obtained from step 2 above (54 g, 189 mmol, 1 eq) in dry THF (500 mL) was cooled to 0° C. CH3MgBr (3 M in THF, 253 mL, 757.8 mmol, 4 eq) was added dropwise. The mixture was stirred at RT overnight. The reaction mixture was quenched with sat. NH4Cl (200 mL) and extracted with EA (300 mL×2). The combined organic layers were washed with brine (300 mL×2), dried over Na2SO4, filtered and concentrated to give a residue. The desired compound (90.4 g, pure) was obtained as a pale yellow oil which was used into the next step without further purification.
1H NMR (400 MHz, CDCl3) δ 7.45 (d, J=8.4 Hz, 2H), 7.11 (d, J=8.4 Hz, 2H), 1.90 (s, 3H), 1.44 (s, 6H).
Step 4. Preparation of compound 1-bromo-3-(4-bromophenyl)-3-methylbutan-2-one
To the solution of compound obtained from step 3 above (46 g, 191 mmol, 1 eq) in DCM/EtOH (250 mL/250 mL) was added Br2 (14.7 mL, 286 mmol, 1.5 eq) dropwise. The mixture was stirred at RT for 3.5 h. The reaction mixture was quenched with sat·Na2SO3 (150 mL). The mixture was extracted with DCM (300 mL×2) and the combined organic layers were washed with brine (300 mL×2), dried over Na2SO4, filtered and concentrated to give a residue. The desired compound (118.8 g, crude) was obtained as a white solid which was used into the next step without further purification.
1H NMR (400 MHz, CDCl3) δ 7.48 (d, J=8.4 Hz, 2H), 7.11 (d, J=8.4 Hz, 2H), 3.82 (s, 2H), 1.52 (s, 6H).
Step 5. Preparation of 4-(2-(4-bromophenyl)propan-2-yl)thiazol-2-amine
To the solution of compound obtained from step 4 above (50 g, 156 mmol, 1 eq) in MeOH (500 mL) was added thiourea (14.3 g, 188 mmol, 1.2 eq). The mixture was stirred at 50° C. for 1.5 h. The mixture was concentrated under reduced pressure. The mixture was extracted with EA (300 mL×2), the combined organic layers were washed with brine (300 mL×2), dried over Na2SO4, filtered and concentrated to give a residue, the residue was purified by PE/EA=10:1 on silica gel chromatography to give pure desired compound (34 g, white solid).
1H NMR (400 MHz, DMSO-d6) δ 7.39 (d, J=8.0 Hz, 2H), 7.14 (d, J=8.0 Hz, 2H), 6.78 (s, 2H), 6.22 (s, 1H), 1.50 (s, 6H). MS (ESI) m/z (M+H)+=297.0.
Step 1. Preparation of compound ethyl 1-(4-bromophenyl)cyclopentane-1-carboxylate
To a solution of compound ethyl 2-(4-bromophenyl)acetate (10 g, 41.3 mmol) in DMF (50 mL), NaH (8.3 g, 207 mmol) was added slowly at 0° C. and then the reaction was stirred at RT for 30 min. 1,4-dibromobutane (8.8 g, 41.3 mmol) was added slowly at RT. The mixture was stirred at RT overnight. The reaction mixture was concentrated to give a residue. The residue was purified by flash silica gel chromatography (PE:EA=1:0 to 5:1). The title compound (7.8 g, yield: 63.8%) was obtained.
MS (ESI) m/z (M+H)+=297.0
Step 2. Preparation of compound 1-(4-bromophenyl)cyclopentane-1-carboxylic acid
To a solution of compound ethyl 1-(4-bromophenyl)cyclopentane-1-carboxylate (7.8 g, 26.3 mmol) in THF (25 mL) were added NaOH (3.2 g, 79 mmol) and H2O (5 mL) and the reaction was stirred at 40° C. overnight. After cooling down, the PH value of the reaction solution was adjusted to 6. The reaction mixture was concentrated to give a residue. The residue was purified by flash silica gel chromatography (PE:EA=1:0 to 1:2). The desired compound (5.6 g, yield: 79.4%) was obtained.
The synthesis of following steps was similar as described in intermediate 1.
Step 1. Preparation of compound methyl 2-(5-bromopyridin-2-yl)-2-methylpropanoate
To a solution of 3-(5-bromopyridin-2-yl)-2-oxopropanoic acid (2 g, 9.26 mmol, 1.0 eq) in DMF (20 mL) was added NaH (1.3 g, 32.4 mmol, 3.5 eq) at 0° C. The resulting mixture was stirred for 20 min at 0° C. The mixture was added CH3I (2 mL, 3.5 eq) at 0° C. and stirred for 6 h. The reaction mixture was quenched with water (50 mL), extracted with EA (25 mL×2) and washed with brine (10 mL×2), then dried over Na2SO4, filtered and evaporated to dryness. The resulting residue was purified by column chromatography on a silica gel to obtain the desired compound (1.95 g, yield: 93%).
Step 2. Preparation of compound 2-(5-bromopyridin-2-yl)-2-methylpropanoic acid
A mixture of 2-(5-bromopyridin-2-yl)-2-methylpropanoate (1.95 g, 7.56 mmol, 1.0 eq) and KOH (1.9 mL, 2M in H2O, 3.0 eq) was heated to reflux for 1 h. The reaction was cooled to RT and quenched with 0.1M HCl, extracted with EA, washed by brine, dried over Na2SO4, filtered and evaporated to dryness to obtain the desired compound (1.82 g, yield: 98%).
The next few steps are similar as described for intermediate 1.
The following examples were synthesized analogous to the procedure of intermediate 1 using the appropriate starting materials and thiourea:
1H NMR (400 MHz, CDCl3) δ 7.67 (t, J = 1.88 Hz, 1 H), 7.43 (d, J = 7.78 Hz, 1 H), 7.33 − 7.39 (m, 1 H), 7.14 − 7.22 (m, 1 H), 6.48 (s, 1 H), 4.87 (br s, 2 H), 2.57 (s, 1 H), 1.91 (s, 3 H).
1H NMR (400 MHz, CDCl3) δ 7.45 − 7.41 (m, 2H), 7.22 − 7.17 (m, 2H), 6.05 (s, 1H), 4.88 (s, 2H), 2.74 − 2.65 (m, 2H), 2.62 - 2.51 (m, 2H), 2.20 − 2.04 (m, 1H), 1.97 − 1.85 (m, 1H).
Appropriately substituted compound M7 wherein R was suitable 1-3 groups like halo or C1-C6 alkyl, etc, was acetylated with lithium base at lower than −60° C. condition. M9 was obtained by alkyl substitution like C1-C6 alkyl group, of M8 under base condition at 50-70° C. After bromination, M10 was obtained. The cyclization of M10 with thiourea under base condition gave the thiazole intermediate M11. An appropriate protection group was introduced to protect amino. The reduction of ester into alcohol was performed by LiBH4 at 0° C. yielding M13, which was oxidized to the corresponding aldehyde by using Dess-Martin Periodinane (DMP) reagent. The alkynylthiazole amine intermediate M15 was obtained by Seyferth-Gilbert Homologation with treating M14 with 1-diazo-1-dimethoxyphosphoryl-propan-2-one under base condition at RT. The final de-protection gave the intermediate M16.
Step 1. Preparation of compound methyl 2-(4-chlorophenyl)-3-oxobutanoate
To a solution of compound methyl 2-(4-chlorophenyl)acetate (10 g, 54.2 mmol, 8.77 mL) in THF (80 mL) was added dropwise LiHMDS (1M, 65.0 mL) at −78° C. The mixture was stirred at −78° C. for 20 min. Then acetyl acetate (5.53 g, 54.17 mmol, 5.07 mL) was added at −78° C. The mixture was warmed to 0° C. and stirred for 2 h at 0° C. The mixture was quenched with sat. NH4Cl (200 mL) and extracted with EA (100 mL×3). The combined organic layers were washed with brine (200 mL), dried over anhydrous Na2SO4, filtered and concentrated to give a residue. The residue was purified by flash silica gel chromatography (PE:EA=1:0 to 5:1). The desired compound (7.47 g, yield: 60.9%) was obtained as a pale yellow oil.
MS (ESI) m/z (M+H)+=227.1.
Step 2. Preparation of compound methyl 2-(4-chlorophenyl)-2-methyl-3-oxobutanoate
To a solution of compound obtained from step 1 above (7.47 g, 33.0 mmol) and K2CO3 (22.8 g, 165 mmol) in acetone (60 mL) was added iodomethane (13.10 g, 92.28 mmol, 5.74 mL). The mixture was stirred at 70° C. for 16 h. The mixture was filtered and the filtrate was concentrated to give a residue. The desired compound (7.79 g, yield: 98.2%) was obtained as a pale yellow oil which was used into the next step without further purification.
MS (ESI) m1 (M+H)+=241.1.
Step 3. Preparation of compound methyl 4-bromo-2-(4-chlorophenyl)-2-methyl-3-oxobutanoate
To a solution of compound obtained from step 2 above (7.79 g, 32.4 mmol) in CHCl3 (80 mL) was added Br2 (4.66 g, 29.1 mmol, 1.50 mL). The mixture was stirred at 75° C. for 16 h. The reaction mixture was adjust to PH=6-7 with NaOH (1 N), and then washed with H2O (100 mL), brined (100 mL), dried over anhydrous Na2SO4, filtered and concentrated to give a residue. The desired compound (9.91 g, yield: 95.8%) was obtained as a pale brown oil, which was used into the next step without further purification.
MS (ESI) m/z (M+H)+=319.0.
Step 4. Preparation of compound methyl 2-(2-aminothiazol-4-yl)-2-(4-chlorophenyl)propanoate
To a solution of compound obtained from step 3 above (9.91 g, 31.0 mmol) and thiourea (2.83 g, 37.2 mmol) in MeOH (60 mL) was added NaHCO3 (3.13 g, 37.2 mmol, 1.45 mL). The mixture was stirred at 50° C. for 1 h. The reaction mixture was concentrated to give a residue. The precipitate was triturated in H2O (100 mL) and collected by filtration. The desired compound (8.49 g, yield: 92.3%) was obtained as a brown solid.
MS (ESI) nm/z (M+H)+=297.0.
Step 5. Preparation of compound methyl 2-(2-acetamidothiazol-4-yl)-2-(4-chlorophenyl)propanoate
To a solution of compound obtained from step 4 above (3 g, 10.1 mmol) and TEA (1.53 g, 15.2 mmol, 2.11 mL) in DCM (60 mL) was added acetyl chloride (794 mg, 10.11 mmol, 721 uL) at 0° C. The mixture was stirred at 25° C. for 1.5 h. The second batch of acetyl chloride (794 mg, 10.1 mmol, 721 uL) and TEA (1.53 g, 15.2 mmol, 2.11 mL) was added at 0° C., the mixture was stirred at 25° C. for 1 h. The third batch of acetyl chloride (793.5 mg, 10.11 mmol, 721.38 uL) and TEA (1.53 g, 15.16 mmol, 2.11 mL) was added at 0° C., the mixture was stirred at 25° C. for 1.5 h. The reaction mixture was quenched with H2O (3 mL) and then added anhydrous Na2SO4, filtered and concentrated to give a residue. The residue was purified by flash silica gel chromatography (PE:EA=1:0 to 2:1). The desired compound (1.4 g, yield: 32.6%) was obtained as a pale yellow solid.
MS (ESI) m/z (M+H)+=339.1.
Step 6. Preparation of compound N-(4-(2-(4-chlorophenyl)-1-hydroxypropan-2-yl)thiazol-2-yl)acetamide
To a solution of compound obtained from step 5 above (1.4 g, 4.13 mmol) in THF (50 mL) was added partly LiBH4 (450 mg, 20.66 mmol). The mixture was stirred at 25° C. for 16 h. The reaction mixture was quenched with sat. NH4Cl (40 mL) and then extracted with EA (30 mL×3), the combined organic layer was washed with brine (60 mL), dried over anhydrous Na2SO4, filtered and concentrated to give a residue. The residue was purified by flash silica gel chromatography (PE:EA=1:0 to 2:3). The desired compound (970 mg, yield: 73.4%) was obtained as a pale yellow solid.
MS (ESI) m/z (M+H)+=311.1.
Step 7. Preparation of compound N-(4-(2-(4-chlorophenyl)-1-oxopropan-2-yl)thiazol-2-yl)acetamide
To a solution of compound obtained from step 6 above (970 mg, 3.12 mmol) in DCM (30 mL) was added partly DMP (1.72 g, 4.06 mmol) in DCM (20 mL). The mixture was stirred at 25° C. for 2 h. DMP (1.72 g, 4.06 mmol) in DCM (20 mL) was added and the mixture was stirred at 25° C. for 1 h. DMP (1.06 g, 2.50 mmol) in DCM (20 mL) was added and the mixture was stirred at 25° C. for 2 h. The reaction mixture was diluted with DCM (40 mL), quenched with sat. Na2S2O3/sat. NaHCO3(1/1, 200 mL), the organic layer was separated and the aqueous layer was extracted with DCM (60 mL), the combined organic layers were washed with sat. Na2S2O3/sat. NaHCO3 (1/1, 100 mL), water (200 mL×2), brine (200 mL×2), dried over anhydrous Na2SO4, filtered and concentrated to give a residue. The desired compound (1.03 g, crude) was obtained as a yellow solid which was used into the next step without further purification.
Step 8. Preparation of compound N-(4-(2-(4-chlorophenyl)but-3-yn-2-yl)thiazol-2-yl)acetamide
To a solution of compound obtained from step 7 above (1.03 g, 3.34 mmol) and 1-diazo-1-dimethoxyphosphoryl-propan-2-one (961 mg, 5.00 mmol) in MeOH (40 mL) was added K2CO3 (922 mg, 6.67 mmol). The mixture was stirred at 25° C. for 12 h. The reaction mixture was concentrated to give a residue. The residue was purified by flash silica gel chromatography (PE:EA=1:0 to 1:1). The residue was purified by prep-HPLC (column: Venusil ASB Phenyl 150×30 mm×5 um; mobile phase: [water (0.05% HCl)-ACN]; B %: 55%-85%, 9 min). The desired compound (219 mg, yield: 21.54%) was obtained as a white solid.
1H NMR (400 MHz, CDCl3) δ 9.98 (br s, 11), 7.45 (d, J 8.5 Hz, 211), 7.30 (d, J=8.5 Hz, 2H), 6.88 (s, 1H), 2.63 (s, 1H), 2.25 (s, 3H), 1.99 (s, 3H). MS (ESI) m/z (M+H)+=305.1.
Step 9. Preparation of compound 4-(2-(4-chlorophenyl)but-3-yn-2-yl)thiazol-2-amine
To a solution of compound obtained from step 8 above (180 mg, 591 umol) in MeOH (10 mL) was added methanesulfonic acid (284 mg, 2.95 mmol, 210 μL). The mixture was stirred at 80° C. for 16 h. The reaction mixture was adjusted pH=9-10 with solid NaHCO3 and concentrated to give a residue. The residue was purified by flash silica gel chromatography (PE:EA=1:0 to 2:1). The desired compound (137 mg, yield: 88.3%) was obtained as a pale yellow solid.
1H NMR (400 MHz, CDCl3) δ 7.39-7.32 (m, 2H), 7.20-7.16 (m, 2H), 6.35 (s, 1H), 4.90 (br s, 2H). 2.46 (s, 1H), 1.82 (s, 3H). MS (ESI) m/z (M+H)+=263.0.
The following examples were synthesized analogous to the procedure of example 4 (intermediate 27) using the appropriate starting materials and thiourea:
1H NMR (400 MHz, DMSO-d6) δ 7.52 − 7.46 (m, 1H), 7.45 − 7.39 (m, 2H), 6.93 (s, 2H), 6.42 (s, 1H), 3.44 (s, 1H), 1.84 (s, 3H). 19F NMR (376 MHz, DMSO- d6) δ −107.657
1H NMR (400 MHz, DMSO-d6) δ 7.60 − 7.58 (m, 2 H), 7.43 − 7.39 (m, 2 H), 6.74 (s, 1 H), 3.77 (s, 1 H), 2.32 − 2.23 (m, 1 H), 2.18 − 2.11 (m, 1 H), 0.83 (t, J = 7.2 Hz, 3 H)
Step 1. Preparation of compound N-(4-(2-(4-bromophenyl)-1-methoxypropan-2-yl)thiazol-2-yl)acetamide
To a solution of N-(4-(2-(4-bromophenyl)-1-hydroxypropan-2-yl)thiazol-2-yl) acetamide (200 mg, 563 μmol, synthesized in the similar method described in intermediate 46) and N1,N1,N8,N8-tetramethylnaphthalene-1,8-diamine (603 mg, 2.81 mmol) in DCM (10 mL) was added trimethyloxonium; tetrafluoroborate (416 mg, 2.8 mmol) at 0° C. The mixture was stirred at 25° C. for 16 h. The reaction mixture was diluted with DCM (10 mL), quenched with NH3·H2O (10 mL), washed with H2O (30 mL), HCl (1 N, 20 mL), sat. NaHCO3 (20 mL) and brine (40 mL), dried over anhydrous Na2SO4, filtered and concentrated to give a residue. The residue was purified by flash silica gel chromatography (PE:EA=1:0 to 1:1). The desired compound (41 mg, yield: 19.72%) was obtained as a white solid.
1H NMR (400 MHz, CDCl3) δ 8.69 (br s, 1H), 7.39 (d, J=8.5 Hz, 2H), 7.10 (d, J=8.5 Hz, 2H), 6.69 (s, 1H), 3.80 (s, 2H), 3.34 (s, 3H), 2.20 (s, 3H), 1.68 (s, 3H). MS (ESI) m/z (M+H)+=371.0.
Step 2. Preparation of compound 4-(2-(4-bromophenyl)-1-methoxypropan-2-yl) thiazol-2-amine
The synthesis is similar as described in intermediate 44. The desired compound (20 mg, yield: 90.3%) was obtained as a white solid.
1H NMR (400 MHz, CDCl3) δ 7.42-7.36 (m, 2H), 7.18-7.13 (m, 2H), 6.22 (s, 1H), 4.83 (br s, 2H), 3.84-3.73 (m, 2H), 3.34 (s, 3H), 1.65 (s, 3H). MS (ESI) m/z (M+H)+=327.0.
The following intermediates were synthesized analogous to the procedure of example 5 (intermediate 33) using the appropriate starting
Step 1. Preparation of compound 1-(4-bromophenyl)propane-1,2-dione
To a solution of compound 1-(4-bromophenyl)propan-2-one (2.0 g, 9.4 mmol, 1.0 eq) in dioxane (20 mL) was added SeO2 (3.12 g, 28.1 mmol, 3.0 eq). The mixture was stirred at 110° C. for 4 h. After cooling down, the reaction mixture was concentrated to give a residue. The residue was purified by flash silica gel chromatography (PE:EA=96%: 4%). The desired compound (960 mg, yield: 45%) was obtained as a yellow oil.
Step 2. Preparation of compound 3-bromo-1-(4-bromophenyl)propane-1,2-dione
To a solution of compound obtained from step 1 above (960 mg, 4.23 mmol, 1.0 eq) in CH3C1 (20 mL) was added Br2 (1.05 g, 6.34 mmol, 1.5 eq) and AcOH (3 drops). The mixture was stirred at 60° C. for 16 h. The reaction mixture was quenched by sat·Na2SO3 (aq) (20 mL), extracted with DCM (20 mL×2) and washed with brine (15 mL), then dried over Na2SO4, filtered and evaporated to dryness. The residue was purified by flash silica gel chromatography (PE:EA=94%: 6%). The desired compound (800 mg, yield: 74%) was obtained as a yellow oil.
Step 3. Preparation of compound (2-aminothiazol-4-yl)(4-bromophenyl)methanone
To a solution of compound obtained from step 2 above (800 mg, 2.62 mmol, 1.0 eq) in MeOH (8 mL) was added thiourea (200 mg, 2.62 mmol, 1.0 eq) and NaHCO3. The mixture was stirred at 50° C. for 1.5 h. The mixture was concentrated under reduced pressure, extracted with EA (15 mL×2), the combined organic layers were washed with brine (10 mL×2), dried over Na2SO4, filtered and concentrated to give a residue, which was purified by flash silica gel chromatography (PE:EA=3:1) to get the desired group (680 mg, yield: 90%).
Step 4 Preparation of compound 1-(2-aminothiazol-4-yl)-1-(4-bromophenyl)ethan-1-ol
The solution of compound (2-aminothiazol-4-yl)(4-bromophenyl)methanone (200 mg, 0.71 mmol, 1.0 eq) in dry THF (4 mL) was cooled to 0° C., and was added CH3MgBr (3 M in THF, 1.6 mL, 4.9 mmol, 7.0 eq) dropwise. The mixture was stirred at RT overnight. The reaction mixture was quenched with sat. NH4Cl (200 mL), The mixture was extracted with EA (20 mL×2), the combined organic layers were washed with brine (10 mL×2), dried over Na2SO4, filtered and concentrated to give a residue. The resulting residue was purified by Prep-TLC to give the desired compound (40 mg, yield: 20%).
1H NMR (400 MHz, DMSO) δ 7.45-7.38 (m, 2H), 7.22 (t, J=7.5 Hz, 2H), 7.12 (t, J=7.3 Hz, 1H), 6.77 (s, 2H), 6.30 (s, 1H), 5.37 (s, 1H), 1.67 (s, 3H).
MS (ESI) m/z (M+H)+=221.0
Step 1. Preparation of compound N-(5-bromo-4-(2-(4-chlorophenyl)but-3-yn-2-yl)thiazol-2-yl)acetamide
The mixture of N-[4-[1-(4-chlorophenyl)-1-methyl-prop-2-ynyl]thiazol-2-yl]acetamide (1 g, 3.28 mmol) and NBS (700.74 mg, 3.94 mmol) in DMF (10 mL) was stirred at 50° C. for 2 h. The reaction was cooled to room temperature and then diluted with H2O (50 mL), extracted with EtOAc (30 mL×3), the organic phase was combined and washed with brine (50 mL×3), concentrated to give a residue. The residue was purified by flash silica gel chromatography (PE:EA=1:0 to 3:1). The desired compound (800 mg, yield: 52.6%) was obtained as a yellow solid.
1H NMR (400 MHz, CDCl3) δ 8.89 (br. s, 1H), 7.33-7.41 (m, 2H), 7.24-7.32 (m, 2H), 2.61 (s, 1H), 2.29 (s, 3H), 2.00 (s, 3H). MS (ESI) m/z (M+H)+=384.8.
Step 2. Preparation of compound 4-[1-(4-chlorophenyl)-1-methyl-prop-2-ynyl]-5-deuterio-thiazol-2-amine
The mixture of compound obtained from step 1 above (600 mg, 1.56 mmol) and MsOH (751.43 mg, 7.82 mmol) in CD3OD (8 mL) was stirred at 80° C. for 16 h. The reaction was adjusted to pH=8-9 with sat. NaHCO3 aqueous, and then extracted with EtOAc (30 mL×3), the organic phase was combined and washed with brine (30 mL), concentrated to give a residue. The residue was purified by silica gel chromatography (PE:EA=1:0 to 3:1) to give the products, which was re-purified by Pre-TLC (PE:EA=3:1). The desired compound (100 mg, yield: 20.8%) was obtained as a yellow oil.
1H NMR (400 MHz, CDCl3) δ 8.89 (br. s, 1H), 7.33-7.41 (m, 2H), 7.24-7.32 (m, 2H), 2.61 (s, 1H), 2.29 (s, 3H), 2.00 (s, 3H). MS (ESI) m/z (M+H)+=263.8.
At the same time, the byproduct 5-bromo-4-[1-(4-chlorophenyl)-1-methyl-prop-2-ynyl]thiazol-2-amine (300 mg, yield: 52.2%) was obtained as a yellow solid.
MS (ESI) m/z (M+H)+=343.1.
To a solution of thiazole amines (1 eq) and in appropriate organic solvent like DMF was added NaH (1.2-1.5 eqiv.) at 0-10° C., the resulting mixture was stirred for 5-30 mins. The mixture was added activated amine by CDI and stirred for 4-16 hours. Once the reaction was completed, the resulting suspension was diluted with organic solvent and washed with brine and then dried. After filtration and evaporation, the resulting residue was purified by trituration/Prep-TLC/chromatography/Prep-HPLC to give the product.
To a solution of 4-(2-(4-chloro-3-fluorophenyl)propan-2-yl)thiazol-2-amine (40 mg, 0.15 mmol, 1 eq) and in DMF (5 mL) was added NaH (7 mg, 0.3 mmol, 2 eq) at 10° C. The resulting mixture was stirred for 5 min. The mixture was added tert-butyl 4-(4-((1H-imidazole-1-carboxamido)methyl)phenyl)piperazine-1-carboxylate (58 mg, 0.15 mmol, 1 eq), and stirred overnight. The reaction was quenched with water, extracted with EA and combined organic layers were washed with brine then dried (Na2SO4), filtered and evaporated to dryness. The resulting residue was purified by Prep-TLC (PE:EA=3:1) to give the title compound 35 mg (0.06 mmol) with the yield 40%. MS (ESI) m/z (M+H)+=588.2
To a solution of amine fragment (1 eq) and pyridine in appropriate solvent like dry DCM was added phenyl carbonochloridate (2 eq) below 20° C. slowly. The mixture was stirred at RT for 4-6 h. Once the reaction was completed, the resulting reaction was diluted with organic solvent and washed with brine and then dried. After filtration and evaporation, the resulting residue was purified by trituration/Prep-TLC/chromatography/Prep-HPLC to give the product.
Phenyl carbonochloridate (336 mg, 2.2 mmol, 269.0 μL) was added to the mixture of tert-butyl 4-(5-(aminomethyl)pyrimidin-2-yl)piperazine-1-carboxylate (600 mg, 2.1 mmol), pyridine (194 mg, 2.5 mmol, 198 μL) in CH3CN (15 mL) at −20° C. After addition, the mixture was allowed to warm to 25° C. and stirred at 25° C. for 0.25 h. The solvent was removed under vacuum. The residue was triturated with ice water (15 mL). White solid was precipitated from the mixture. The mixture was filtered and the solid was collected, dried under vacuum. Tert-butyl 4-(5-(((phenoxycarbonyl)amino)methyl)pyrimidin-2-yl)piperazine-1-carboxylate (420 mg, yield: 38.2%) was obtained as a white solid. MS (ESI) m/z (M+H)+=414.2.
To the mixture of tert-butyl 4-(5-(((phenoxycarbonyl)amino)methyl)pyrimidin-2-yl) piperazine-1-carboxylate (139 mg, 336 μmol) and 4-(2-(4-bromophenyl) propan-2-yl)thiazol-2-amine (50 mg, 168 μmol) in DCE (10 mL) was added DMAP (41.0 mg, 337.0 μmol, 2 eq). The mixture was stirred at 85° C. for 16 h. The mixture was concentrated under vacuum. The residue was purified by prep-TLC (SiO2, DCM:MeOH=13:1) and further purified by prep-TLC (SiO2, DCM:MeOH=12:1). The desired compound (60 mg, yield: 57.7%) was obtained as a white solid.
MS (ESI) m/z (M+H)+=616.2.
To a solution of substituted thiazol-2-amine and hunig base or pyridine in appropriate solvent like DCM or CH3CN, or DCM/water was added phenyl carbonochloridate (2 eq) at 0° C.-RT slowly. The mixture was stirred 2-4 h at RT and the resulting reaction was diluted with organic solvent and washed with brine and then dried. After filtration and evaporation, the resulting residue was purified by chromatography to give the substituted thiazol-2-amine carbamate.
The mixture of the substituted thiazol-2-amine carbamate, amine and DMAP in appropriate solvent like THF was heated to reflux for 1-2 h. After cooling down, the resulting reaction evaporated and diluted with appropriate organic solvent like EA and washed with brine and then dried. After filtration and evaporation, the resulting residue was purified by trituration/Prep-TLC/chromatography/Prep-HPLC to give the product.
To a solution of 4-(2-(4-bromophenyl)propan-2-yl)thiazol-2-amine (100 mg, 0.34 mmol, 1 eq) and triethylamine in dry DCM (5 mL) was added phenyl carbonochloridate (106 mg, 0.68 mmol, 2 eq) at 0° C.-RT slowly and the mixture was stirred for 4 h at RT. Quenched by brine, extracted with EA, the combined organic layers were washed with brine, dried over Na2SO4, filtered and concentrated to give a residue, which was purified by column chromatography on a silica gel to afford phenyl (4-(2-(4-bromophenyl)propan-2-yl)thiazol-2-yl)carbamate (112 mg).
The mixture of phenyl (4-(2-(4-bromophenyl)propan-2-yl)thiazol-2-yl)carbamate (112 mg, 0.27 mmol, 1 eq), tert-butyl ((1-(4-(aminomethyl)phenyl)piperidin-4-yl)methyl)carbamate (24 mg, 0.27 mmol, 1 eq) and DMAP (52 mg, 0.4 mmol, 1.5 eq) in THF (5 mL) was heated to reflux for 1 hour. Cooled down to RT, the reaction mixture was participated between H2O (15 mL) and EA (10 mL×2), the combined organic layers were washed with brine (10 mL), dried over Na2SO4, filtered and concentrated. The residue was purified by column chromatography on a silica gel to afford tert-butyl ((1-(4-((3-(4-(2-(4-bromophenyl)propan-2-yl)thiazol-2-yl)ureido)methyl)phenyl)piperidin-4-yl)methyl)carbamate (42 mg) as a white powder.
The mixture of amine and isocyanate-alkanes in THF was stirred at RT overnight. Once the reaction was completed, the resulting suspension was diluted with organic solvent and washed with brine and then dried. After filtration and evaporation, the resulting residue was purified by trituration/Prep-TLC/Prep-HPLC to give the product.
To a solution of 4-(2-(4-methoxyphenyl)propan-2-yl)thiophen-2-amine (200 mg, 0.67 mmol) in THF (5 mL), was added isocyanatoethane (48 mg, 0.67 mmol) and TEA (136 mg, 1.34 mmol). The resulting mixture was stirred at RT overnight. The mixture was concentrated at 45° C. with reduce pressure to remove THF. The resulting suspension was diluted with EtOAc and washed with brine and then dried (Na2SO4), filtered and evaporated to dryness. The resulting residue was purified by Prep-TLC to give the desired compound (164 mg, yield: 65.4%) as a pale yellow solid. MS (ESI) m/z (M+H)+=367.1.
De-BOC General Method
The Boc compounds were dissolved in HCl/MeOH, the reaction mixture was stirred for 1-2 h at RT. The solution was concentrated to dryness to give the final compound.
To a solution of tert-butyl 4-(5-((3-(4-(2-(4-bromophenyl)propan-2-yl)thiazol-2-yl)ureido)methyl)pyridin-2-yl)piperazine-1-carboxylate (70.0 mg, 113.71 μmol) in MeOH (2 mL) was added HCl/MeOH (4 M, 2 mL). The mixture was stirred at 25° C. for 1 hr. The mixture was concentrated in vacuum. The desired compound (47.0 mg, yield: 74.1%, HCl) was obtained as a white solid.
1H NMR (400 MHz, DMSO-d6) δ 10.90 (br s, 1H), 9.66 (br s, 2H), 8.05-7.92 (m, 2H), 7.48-7.28 (m, 4H), 7.21-7.10 (m, 2H), 6.75 (s, 1H), 4.30-4.20 (m, 2H), 4.04-3.92 (m, 4H), 3.24 (br s, 4H), 1.57 (s, 6H). MS (ESI) m/z (M+H)+=517.2.
The following examples were synthesized analogous to the procedure of example 8, 9, 10, 11 and 12 using the appropriate intermediates and the corresponding fragments:
1H NMR (400 MHz, CDCl3) δ 7.40-7.35 (m, 2H), 7.15-7.10 (m, 2H), 6.42 (s, 1H), 4.54-4.49 (m, 1H), 4.41-4.37 (m, 1H), 3.55 (ddd, J = 28.1, 10.0, 5.2 Hz, 2H), 1.63 (s, 6H).
1H NMR (400 MHz, DMSO-d6) δ 10.53 (s, 1H), 7.12-7.00 (m, 2H), 6.83- 6.68 (m, 2H), 6.60 (s, 1H), 6.48 (s, 1H), 4.40 (dt, J = 47.5, 5.0 Hz, 2H), 3.72- 3.58 (m, 3H), 3.37 (ddd, J =
1H NMR (400 MHz, CD3OD) δ 7.85 (dd, J = 9.3, 1.9 Hz, 1H), 7.75 (s, 1H), 7.20-7.15 (m, 2H), 7.08 (d, J = 9.3 Hz, 1H), 6.87-6.81 (m, 2H), 6.78 (s, 1H), 4.31 (s, 2H), 3.85- 3.78 (m, 2H), 3.78-3.73 (m, 3H), 3.55-3.48 (m, 2H), 1.67 (s, 6H).
1H NMR (400 MHz, CD3OD) δ 7.94 (dd, J = 9.5, 2.1 Hz, 1H), 7.84 (d, J = 1.6 Hz, 1H), 7.31 (d, J = 9.5 Hz, 1H), 7.21-7.16 (m, 2H), 6.88-6.85 (m, 1H), 6.85 (d, J = 2.1 Hz, 1H), 6.84 (s, 1H), 4.35 (s, 2H), 3.85 (t, J = 4.8 Hz, 2H), 3.80-3.77 (m, 2H), 3.77 (s, 3H), 3.29 (s, 3H), 1.68 (s,
1H NMR (400 MHz, CDCl3) δ 7.44-7.37 (m, 2H), 7.30- 7.24 (m, 2H), 6.75 (s, 1H), 3.55-3.40 (m, 2H), 2.58- 2.51 (m, 3H), 1.92 (s, 3H).
1H NMR (400 MHz, CD3OD) δ 7.45 (d, J = 6.9 Hz, 2H), 7.22 (s, 2H), 7.14 (s, 2H), 6.97 (s, 3H), 4.32 (s, 2H), 4.18 (s, 1H), 3.37 (s, 4H), 3.33 (s, 4H), 1.59 (s, 3H).
1H NMR (400 MHz, DMSO-d6) δ 9.28 (s, 1H), 7.39 (d, J = 8.3 Hz, 2H), 7.19 (d, J = 8.5 Hz, 2H), 7.13 (d, J = 8.3 Hz, 2H), 6.93 (d, J = 8.5 Hz, 2H), 6.76 (s, 1H), 4.18 (d, J = 4.4 Hz, 2H), 3.31 (s, 4H), 3.16 (s, 4H), 2.41 (d, J = 12.9 Hz, 2H), 1.95 (s, 2H), 1.59 (d, J = 9.0 Hz, 4H).
1H NMR (400 MHz, DMSO-d6) δ 8.99 (s, 1H), 7.26 (d, J = 8.5 Hz, 2H), 7.17 (d, J = 8.4 Hz, 2H), 7.12 (d, J = 8.2 Hz, 2H), 6.91 (d, J = 8.7 Hz, 3H), 6.70 (s, 1H), 4.17 (d, J = 5.8 Hz, 2H), 3.28 (s, 4H), 3.17 (s, 4H), 1.54 (s, 6H).
1H NMR (400 MHz, DMSO-d6) δ 7.18 (dd, J = 8.1, 5.7 Hz, 2H), 7.12 (d, J = 8.2 Hz, 2H), 7.01 (t, J = 8.6 Hz, 2H), 6.89 (d, J = 8.1 Hz, 2H), 6.84 (s, 1H), 6.66 (s, 1H), 4.17 (d, J = 5.6 Hz, 2H), 3.24 (d, J = 5.3 Hz, 4H), 3.13 (d, J = 5.0 Hz, 4H), 1.54 (s, 6H).
1H NMR (400 MHz, DMSO-d6) δ 9.24 (s, 1H), 7.39 (d, J = 8.6 Hz, 2H), 7.19 (d, J = 8.6 Hz, 1H), 7.12 (d, J = 8.6 Hz, 3H), 7.01 (d, J = 2.3 Hz, 1H), 6.90 (dd, J = 8.7, 2.3 Hz, 1H), 6.70 (s, 1H), 4.25 (d, J = 5.7 Hz, 2H), 3.43-3.28 (m, 4H), 3.13 (s, 4H), 1.54 (s, 6H).
1H NMR (400 MHz, DMSO-d6) δ 9.11 (s, 2H), 7.54 (d, J = 9.0 Hz, 2H), 7.46 (d, J = 8.1 Hz, 1H), 7.38 (d, J = 8.5 Hz, 2H), 7.19 (s, 1H), 7.11 (d, J = 8.5 Hz, 2H), 6.70 (s, 1H), 4.30 (d, J = 5.7 Hz, 2H), 3.10 (d, J = 17.0 Hz, 4H), 3.01 (d, J = 3.9 Hz, 4H), 1.56 (d, J = 22.5 Hz, 6H).
1H NMR (400 MHz, DMSO-d6) δ 9.31 (s, 1H), 7.31 (d, J = 44.6 Hz, 3H), 7.04 (d, J = 44.4 Hz, 4H), 6.68 (s, 1H), 4.18 (s, 2H), 3.15 (s, 8H), 1.51 (s, 6H).
1H NMR (400 MHz, DMSO-d6) δ 10.54-10.45 (m, 1H), 9.02 (s, 1H), 7.39 (d, J = 8.6 Hz, 2H), 7.11 (d, J = 8.6 Hz, 2H), 7.05 (d, J = 8.5 Hz, 1H), 6.78 (s, 2H), 6.74 (d, J = 8.5 Hz, 1H), 6.70 (s, 1H), 4.17 (d, J = 5.4 Hz, 2H), 3.28 (d, J = 5.5 Hz, 4H), 3.16 (s, 4H), 2.20 (s, 3H), 1.54 (s, 6H).
1H NMR (400 MHz, DMSO-d6) δ 9.35 (s, 1H), 8.04 (s, 1H), 7.54-7.32 (m, 3H), 7.23 (d, J = 29.5 Hz, 2H), 7.09 (d, J = 19.3 Hz, 3H), 6.70 (s, 1H), 3.13 (d, J = 46.5 Hz, 8H), 2.66 (d, J = 17.4 Hz, 2H), 1.53 (s, 6H).
1H NMR (400 MHz, DMSO-d6) δ 9.15 (s, 1H), 7.09 (d, J = 18.4 Hz, 4H), 6.90 (s, 2H), 6.75 (s, 2H), 6.61 (s, 1H), 4.17 (s, 2H), 3.65 (s, 3H), 3.28 (s, 4H), 3.15 (s, 4H), 1.52 (s, 6H).
1H NMR (400 MHz, CD3OD) δ 10.12 (s, 2H), 8.12 (s, 1H), 7.81 (d, J = 23.1 Hz, 5H), 7.53 (s, 2H), 7.39 (s, 1H), 4.97 (s, 2H), 4.43 (s, 3H), 3.93 (s, 8H), 2.29 (s, 6H).
1H NMR (400 MHz, CD3OD) δ 7.48 (d, J = 8.4 Hz, 2H), 7.19 (d, J = 7.1 Hz, 2H), 7.11 (s, 1H), 7.00 (s, 2H), 6.93 (s, 1H), 4.38 (s, 2H), 4.19 (s, 4H), 3.77 (s, 4H), 3.43 (s, 4H), 3.40 (s, 3H), 1.69 (s, 6H).
1H NMR (400 MHz, CD3OD) δ 7.46 (d, J = 8.4 Hz, 2H), 7.38 (d, J = 8.5 Hz, 2H), 7.04 (t, J = 9.9 Hz, 4H), 4.36 (d, J = 6.7 Hz, 2H), 3.29 (s, 8H), 1.84 (d, J = 13.6 Hz, 3H).
1H NMR (400 MHz, CD3OD) δ 8.48 (d, J = 2.3 Hz, 1H), 7.80-7.73 (m, 1H), 7.08 (d, J = 8.4 Hz, 1H), 7.01 (d, J = 4.2 Hz, 2H), 6.99 (s, 1H), 6.73 (s, 1H), 4.30 (s, 2H), 3.25 (s, 4H), 3.23 (s, 4H), 1.64 (s, 6H).
1H NMR (400 MHz, CD3OD) δ 7.41 (d, J = 4.2 Hz, 2H), 7.21 (s, 1H), 7.15 (d, J = 6.7 Hz, 1H), 7.12 (d, J = 5.9 Hz, 2H), 6.88 (s, 1H), 6.85 (s, 1H), 6.82 (d, J = 5.7 Hz, 2H), 4.67 (s, 2H), 4.38 (s, 2H), 3.74 (s, 3H), 3.25-3.22 (m, 4H), 3.17- 3.11 (m, 4H), 1.63 (s, 6H).
1H NMR (400 MHz, CD3OD) δ 7.17 (t, J = 5.9 Hz, 2H), 7.09 (dd, J = 9.4, 2.7 Hz, 2H), 6.96 (d, J = 8.7 Hz, 2H), 6.78-6.73 (m, 2H), 6.58 (s, 1H), 4.28 (s, 2H), 3.96 (q, J = 7.0 Hz, 2H), 3.34 (d, J = 3.6 Hz, 4H), 3.33 (s, 4H), 1.57 (s, 6H), 1.37-1.29 (m, 3H).
1H NMR (400 MHz, DMSO-d6) δ 9.35 (s, 2H), 8.05 (s, 1H), 7.53 (d, J = 2.0 Hz, 1H), 7.48 (s, 1H), 7.30 (d, J = 10.1 Hz, 2H), 7.08 (t, J = 8.0 Hz, 3H), 6.78 (d, J = 8.8 Hz, 2H), 6.65 (s, 1H), 4.24 (d, J = 5.2 Hz, 2H), 3.66 (s, 3H), 3.20 (s, 4H), 3.08 (s, 4H), 1.54 (s, 6H).
1H NMR (400 MHz, DMSO-d6) δ 8.08 (s, 3H), 7.49 (s, 1H), 7.40 (d, J = 8.2 Hz, 2H), 7.11 (d, J = 8.2 Hz, 2H), 6.78 (s, 1H), 3.14- 3.12 (s, 2H), 2.73 (s, 2H), 1.70 (s, 2H), 1.53 (s, 6H).
1H NMR (400 MHz, CD3OD) δ 7.22-7.15 (m, 4H), 7.09 (s, 1H), 6.89 (d, J = 8.8 Hz, 2H), 6.64 (d, J = 8.5 Hz, 2H), 4.62 (s, 1H), 4.46 (s, 1H), 4.30 (s, 2H), 3.75 (s, 3H), 3.69 (dd, J = 10.7, 2.2 Hz, 1H), 3.31-
1H NMR (400 MHz, CD3OD) δ 7.70 (d, J = 2.0 Hz, 1H), 7.50 (dd, J = 8.3, 2.0 Hz, 1H), 7.28 (d, J = 8.3 Hz, 1H), 7.23 (s, 1H), 7.20 (s, 1H), 7.14 (s, 1H), 6.93 (d, J = 8.8 Hz, 2H), 4.47 (s, 2H), 3.79 (s, 3H), 3.56- 3.48 (m, 1H), 3.46-3.41 (m, 1H), 3.38 (d, J = 11.9 Hz, 1H), 3.17 (d, J = 12.7 Hz, 1H), 3.00 (d, J = 13.9 Hz, 1H), 2.97-2.91 (m, 1H), 2.90-2.84 (m, 1H), 1.72 (s, 6H), 1.40 (d, J = 6.6
1H NMR (400 MHz, DMSO-d6) δ 10.70 (s, 1H), 9.72 (s, 1H), 8.89 (s, 1H), 7.68 (s, 1H), 7.37 (s, 1H), 7.23 (d, J = 1.9 Hz, 1H), 7.18 (dd, J = 8.5, 1.9 Hz, 1H), 7.13 (d, J = 8.8 Hz, 2H), 6.80 (dd, J = 14.2, 8.7 Hz, 3H), 6.68 (d, J = 1.1 Hz, 1H), 5.44 (s, 5H), 4.48 (s, 1H), 4.35 (s, 1H), 4.22
1H NMR (400 MHz, DMSO-d6) δ 9.42 (s, 1H), 8.45 (s, 1H), 7.51 (d, J = 28.5 Hz, 2H), 7.28 (d, J = 8.0 Hz, 1H), 7.07 (t, J = 10.0 Hz, 3H), 6.78 (d, J = 8.4 Hz, 2H), 6.67 (s, 1H), 4.23 (s, 2H), 3.66 (s, 3H), 3.18 (s, 4H), 3.06 (s, 4H), 2.77 (d, J = 3.7 Hz, 3H), 2.46 (s, 1H), 1.54 (s, 6H).
1H NMR (400 MHz, DMSO-d6) δ 8.46 (br, 5H), 7.39 (d, J = 8.8 Hz, 2H), 7.32 (s, 1H), 7.10 (d, J = 8.8 Hz, 2H), 6.73 (s, 1H), 4.15 (s, 2H), 3.70-3.59 (m, 5H), 2.30-2.27 (m, 1H), 2.16-2.13 (m, 1H), 1.53 (s, 6H).
1H NMR (400 MHz, CDCl3) δ 8.13 (s, 2H), 7.34 (d, J = 8.4 Hz, 2H), 7.05 (d, J = 8.4 Hz, 2H), 6.48 (s, 1H), 4.49 (br s, 1H), 4.07 (br d, J = 4.0 Hz, 2H), 3.85-3.50 (m, 4H), 2.22-1.92 (m, 3H), 1.59 (s, 6H), 1.26 (s, 1H).
1H NMR (400 MHz, DMSO-d6) δ 10.72 (s, 1 H), 8.49 (s, 2 H), 7.39 (d, J = 8.56 Hz, 2 H), 7.14-7.07 (m, 2 H), 6.85-6.79 (m, 1 H), 6.70 (s, 1 H), 4.20 (s, 2 H), 3.82-3.87 (m, 3 H), 1.53 (s, 6 6H).
1H NMR (400 MHz, DMSO-d6) δ 8.44 (s, 2 H), 8.06 (br s, 3 H), 7.43 (d, J = 8.56 Hz, 2 H), 7.24 (br s, 1 H), 7.14 (d, J = 8.56 Hz, 2 H), 6.75 (s, 1 H), 4.17 (br d, J = 5.38 Hz, 2 H), 3.52- 3.65 (m, 2 H), 2.88-3.04 (m, 2 H), 1.57 (s, 6 H).
1H NMR (400 MHz, DMSO-d6) δ 10.65 (s, 1H), 8.27 (s, 2H), 7.42 (d, J = 8.6 Hz, 2H), 7.14 (d, J = 8.8 Hz, 2H), 6.77-6.67 (m, 2H), 4.74-4.68 (m, 1H), 4.27-4.19 (m, 2H), 4.12- 4.06 (m, 2H), 3.75-3.66 (m, 1H), 3.26-3.18 (m, 2H), 1.79-1.71 (m, 2H), 1.57 (s, 6H), 1.31-1.24 (m, 2H).
1H NMR (400 MHz, CDCl3) δ 8.16 (s, 2 H), 7.15- 7.03 (m, 2 H), 6.79-6.77 (m, 1 H), 6.83-6.72 (m, 1 H), 6.46-6.38 (m, 1 H), 4.55-4.49 (m, 1 H), 4.15- 4.06 (m, 2 H), 3.77 (s, 3 H), 3.71-3.59 (m, 4 H), 2.13- 2.02 (m, 2 H), 1.58 (s, 6 H)
1H NMR (400 MHz, DMSO-d6) δ 9.17 (s, 1H), 8.34 (s, 2H), 7.25 (d, J = 8.0 Hz, 2H) ,7.16 (d, J = 8.0 Hz, 2H), 7.02 (s, 1H), 6.69 (s, 1H), 4.11 (s, 2H), 3.90 (s, 4H), 3.09 (s, 4H), 1.53 (s, 6H).
1H NMR (400 MHz, DMSO-d6) δ 9.34 (s, 1H), 8.35 (s, 1H), 7.22 (d, J = 40.8 Hz, 2H), 7.01 (s, 2H), 6.69 (s, 1H), 4.11 (s, 2H), 3.91 (s, 4H), 3.08 (s, 4H), 1.54 (s, 6H).
1H NMR (400 MHz, CD3OD) δ 8.47 (s, 2H), 7.17 (s, 2H), 7.09 (s, 1H), 6.88 (s, 2H), 4.32 (s, 2H), 4.09 (s, 3H), 3.74 (s, 4H), 3.32 (d, J = 5.5 Hz, 4H), 1.67 (s, 6H).
1H NMR (400 MHz, CD3OD) δ 8.57 (s, 2H), 7.15 (d, J = 8.2 Hz, 2H), 7.11 (s, 1H), 6.87 (d, J = 8.2 Hz, 2H), 4.37 (s, 2H), 4.14 (s, 4H), 3.99 (q, J = 6.9 Hz, 2H), 3.34 (d, J = 12.6 Hz, 4H), 1.68 (s, 6H), 1.34 (t, J = 6.9 Hz, 3H).
1H NMR (400 MHz, CD3OD) δ 8.51 (s, 2H), 7.53-7.51 (m, 2H), 7.24- 7.22 (m, 2H), 7.15 (s, 1H), 4.36 (s, 2H), 4.14-4.12 (m, 4H), 3.34-3.33 (m, 4H), 1.73 (s, 6H).
1H NMR (400 MHz, DMSO-d6) δ 01.70 (br s, 1H), 9.37 (br s, 2H), 8.21 (s, 1H), 7.42 (d, J = 8.3 Hz, 2H), 7.34-7.26 (m, 1H), 7.14 (d, J = 8.6 Hz, 2H), 6.75 (s, 1H), 4.20 (br d, J = 5.1 Hz, 2H), 4.01-3.91 (m, 4H), 3.12 (br s, 4H), 2.37 (s, 3H), 1.57 (s, 6H)
1H NMR (400 MHz, DMSO-d6) δ 9.45 (br s, 2H), 8.35 (d, J = 5.1 Hz, 1H), 7.41-7.47 (m, 3H), 7.24- 7.34 (m, 2H), 7.11-7.21 (m, 3H), 6.75 (s, 1H), 6.67 (d, J = 5.1 Hz, 1H), 4.28 (br s, 1H), 4.27 (br s, 1H), 4.05 (s, 1H), 3.05 (s, 1H), 1.58 (s,
1H NMR (400 MHz, DMSO-d6) δ 9.24 (br s, 2H), 8.31 (d, J = 5.0 Hz, 1H), 7.45 (s, 1H), 7.42 (d, J = 3.3 Hz, 2H), 7.29 (s, 1H), 7.17 (d, J = 1.8 Hz, 2H), 7.15-7.14 (m, 1H), 6.74 (s, 1H), 6.64 (d, J = 5.0 Hz, 1H), 4.28 (br d, J = 5.3 Hz, 2H), 4.01 (br s, 2H), 3.20 (br s, 2H), 3.16-3.08 (m, 2H), 2.09-2.01 (m, 2H), 1.58 (s, 6H), 1.26-1.19 (m, 2H).
1H NMR (400 MHz, DMSO-d6) δ 10.90 (br s, 1H), 9.66 (br s, 2H), 8.05- 7.92 (m, 2H), 7.48-7.28 (m, 4H), 7.21-7.10 (m, 2H), 6.75 (s, 1H), 4.30- 4.20 (m, 2H), 4.04-3.92 (m, 4H), 3.24 (br s, 4H), 1.57 (s, 6H).
1H NMR (400 MHz, DMSO-d6) δ 9.26 (s, 2H), 8.30 (s, 1H), 8.07 (s, 2H), 7.41-7.36 (m, 2H), 7.13- 7.11 (m, 3H), 6.72 (s, 1H), 4.29-4.28 (m, 2H), 3.76- 3.74 (m, 4H), 3.16-3.14 (m, 4H), 1.54 (s, 6H).
1H NMR (400 MHz, DMSO-d6) δ 11.05 (br s, 1H), 9.70 (br s, 2H), 8.86 (s, 1H), 7.48-7.43 (m, 2H), 7.39-7.33 (m, 1H), 7.21- 7.14 (m, 3H), 6.78 (s, 1H), 4.45 (br d, J = 6.0 Hz, 2H), 4.11 (br s, 4H), 3.25 (br s, 4H), 1.59 (s, 6H).
1H NMR (400 MHz, DMSO-d6) δ 7.40 (d, J = 8.4 Hz, 2H), 7.13 (d, J = 8.8 Hz, 2H), 6.87 (s, 1H), 6.70 (s, 1H), 6.43 (s, 1H), 4.12 (s, 2H), 3.46-3.39 (m, 4H), 2.69-2.67 (m, 4H), 2.30 (s, 3H), 1.55 (s, 6H).
1H NMR (400 MHz, DMSO-d6) δ 10.61 (br s, 1H), 9.04 (br s, 2H), 7.40 (d, J = 8.8 Hz, 2H), 7.12 (d, J = 8.8 Hz, 2H), 7.07-6.99 (m, 2H), 6.95 (br d, J = 7.6 Hz, 2H), 6.71 (s, 1H), 4.18 (br d, J = 5.6 Hz, 2H), 3.17 (br s, 4H), 2.97 (br d, J = 4.4 Hz, 4H), 2.19 (s, 3H), 1.54 (s, 6H).
1H NMR (400 MHz, CDCl3) δ 9.18 (brs, 2H), 7.43 (d, J = 8.4 Hz, 2H), 7.57-7.29 (m, 1H), 7.18- 7.13 (m, 4H), 6.75 (s, 1H), 4.24 (s, 2H), 3.23-3.14 (m, 8H), 1.58 (s, 6H).
1H NMR (400 MHz, DMSO-d6) δ 10.76 (br, 1H), 9.22 (br, 2H), 7.42- 7.39 (m, 2H), 7.26-7.12 (m, 6H), 6.71 (s, 1H), 4.26- 4.25 (m, 2H), 3.24-3.22 (m, 4H), 3.03-3.02 (m, 4H), 1.55 (s, 6H).
1H NMR (400 MHz, DMSO-d6) δ 10.94-10.50 (m, 1H), 8.34 (s, 2H), 8.25- 7.95 (m, 3H), 7.42 (d, J = 8.5 Hz, 2H), 7.19-6.92 (m, 3H), 6.74 (s, 1H), 4.71- 4.54 (m, 2H), 4.19-4.05 (m, 2H), 3.38-3.24 (m, 1H), 3.04-2.87 (m, 2H), 2.03-1.90 (m, 2H), 1.57 (s, 6H), 1.49-1.35 (m, 2H).
1H NMR (400 MHz, CDCl3) δ 8.57 (br s, 1H), 7.39 (d, J = 8.8 Hz, 2H), 7.13 (d, J = 8.4 Hz, 2H), 6.43 (s, 1H), 3.96-3.82 (m, 1H), 1.64 (s, 6H), 1.10 (d, J = 6.4 Hz, 6H).
1H NMR (400 MHz, CDCl3) δ 7.30-7.26 (m, 2H), 7.15-7.10 (m, 2H), 6.47 (s, 1H), 3.60-3.55 (m, 2H), 3.45-3.30 (m, 2H), 1.63 (s, 6H), 1.40-1.30 (m, 2H).
1H NMR (400 MHz, DMSO-d6) δ 10.50 (br s, 1 H), 7.40 (d, J = 8.56 Hz, 2 H), 7.12 (d, J = 8.56 Hz, 2 H), 6.68 (s, 1 H), 6.29 (br s, 1 H), 3.53 (t, J = 4.52 Hz, 4 H), 3.09 (q, J = 6.60 Hz, 2 H), 2.27 (br s, 4 H), 2.22 (t, J = 6.97 Hz, 2 H) 1.54 (s, 6 H), 1.53-1.47 (m, 2 H).
1H NMR (400 MHz, CDCl3) δ 7.40-7.34 (m, 2H), 7.40-7.34 (m, 2H), 7.08 (d, J = 8.78 Hz, 2 H), 6.56 (br s, 1 H), 5.00-4.84 (m, 1H), 4.12-4.00 (m, 1H), 3.46-3.19 (m, 3H), 3.01-2.74 (m, 3H), 2.40- 2.21 (m, 1H), 2.00-1.82 (m, 2H), 1.64-1.51 (m,
1H NMR (400 MHz, CDCl3) δ 7.38 (d, J = 8.07 Hz, 2 H), 7.10 (d, J = 8.31 Hz, 2 H), 6.47 (s, 1 H), 3.38 (q, J = 6.11 Hz, 2 H), 2.99 (br t, J = 7.58 Hz, 2 H), 2.86 (s, 3 H), 2.03-1.95 (m, 2 H), 1.62 (s, 6 H).
1H NMR (400 MHz, CD3OD) δ 7.38 (d, J = 8.31 Hz, 2 H), 7.16 (d, J = 8.56 Hz, 2 H), 6.66 (s, 1 H), 3.67 (t, J = 6.48 Hz, 2 H), 3.26 (t, J = 6.36 Hz, 2 H), 1.63 (s, 6 H).
1H NMR (400 MHz, CDCl3) δ 7.43-7.35 (m, 2 H), 7.13-7.03 (m, 2 H), 6.53 (s, 1 H), 5.56-5.31 (m, 1 H), 3.34 (d, J = 5.77 Hz, 2 H), 3.03 (s, 2 H), 1.99- 1.89 (m, 2 H), 1.61 (s, 6 H).
1H NMR (400 MHz, DMSO-d6) δ 10.46 (br s, 1 H), 7.11-7.05 (m, 2 H), 6.77 (d, J = 9.05 Hz, 2 H), 6.59 (s, 1 H), 6.32 (br s, 1 H), 3.66 (s, 3 H), 3.53 (br t, J = 4.52 Hz, 4 H), 3.12-3.06 (m, 2 H), 2.27 (br s, 4H), 2.22 (t, J = 6.97 Hz, 2 H), 1.59-1.49 (m, 8 H).
1H NMR (400 MHz, CDCl3) δ 7.08 (d, J = 8.8 Hz, 2H), 6.77 (d, J = 8.8 Hz, 2H), 6.69 (s, 1H), 6.60 (s, 1H), 5.40 (s, 1H), 4.34 (s, 1H), 3.66 (s, 3H), 3.11 (s, 3H), 3.03 (s, 3H), 1.77 (s, 2H), 1.53 (s, 6H), 1.35- 1.15 (m, 2H), 0.95-0.85 (m, 2H).
1H NMR (400 MHz, CD3OD) δ 7.17 (d, J = 8.8 Hz, 2H), 6.82 (d, J = 8.8 Hz, 2H), 6.43 (s, 3H), 3.78 (s, 3H), 3.42-3.38 (m, 2H), 3.00-2.97 (m, 2H), 2.86 (s, 3H), 2.05-1.98 (m, 2H), 1.64 (s, 3H)
1H NMR (400 MHz, CD3OD) δ 7.18 (d, J = 8.8 Hz, 2H), 7.25 (d, J = 8.4 Hz, 2H), 6.61 (s, 1H), 3.77 (s, 3H), 3.72-3.66 (m, 2H), 3.30-3.25 (m, 2H), 1.65 (s, 6H).
1H NMR (400 MHz, CD3OD) δ 7.17 (d, J = 8.8 Hz, 2H), 6.83 (d, J = 8.0 Hz, 2H), 6.63 (s, 1H), 3.77 (s, 3H), 3.39-3.35 (m, 2H), 3.15-3.02 (m, 2H), 2.12- 2.00 (m, 2H), 1.65 (s, 6H).
1H NMR (400 MHz, DMSO-d6) δ 10.48 (s, 1 H), 7.09 (dd, J = 12.59, 8.68 Hz, 4 H), 6.87 (d, J = 8.56 Hz, 2 H), 6.79 (d, J = 9.05 Hz, 2 H), 6.68 (br s, 1 H), 6.63 (s, 1 H), 4.67 (d, J = 4.16 Hz, 1 H), 4.17 (d, J = 5.87 Hz, 2 H), 3.69 (s, 3 H), 3.59 (td, J = 8.80, 4.40 Hz, 1 H), 3.51- 3.44 (m, 2 H), 2.83-2.72 (m, 2 H), 1.82-1.73 (m, 2 H), 1.56 (s, 6 H), 1.52- 1.34 (m, 2 H).
1H NMR (400 MHz, CDCl3) δ 7.25-7.22 (m, 2H), 7.18-7.10 (m, 4H), 6.83-6.73 (m, 2H), 6.45 (s, 1H), 4.57 (s, 2H), 4.31- 4.29 (m, 2H), 3.76 (s, 3H), 1.59 (s, 6H).
1H NMR (400 MHz, DMSO-d6) δ 10.43 (s, 1H) 7.08 (d, J = 8.82 Hz, 2H) 6.77 (d, J = 8.82 Hz, 2H) 6.58 (s, 1H) 6.36 (s, 1H) 3.66 (s, 3H) 3.08 (q, J = 6.39 Hz, 2H) 2.57-2.70 (m, 2H), 2.50-2.56 (m, 1H) 2.23- 2.40 (m, 3H) 2.19 (t, J = 7.06 Hz, 1H) 2.05 (s, 6H) 1.73-1.84 (m, 1H) 1.44-1.60
1H NMR (400 MHz, DMSO-d6) δ 10.49 (br, 1H), 7.14-7.12 (m, 2H), 6.83- 6.80 (m, 2H), 6.63 (s, 1H), 6.34 (br, 1H), 3.73 (s, 3H), 3.14-3.09 (m, 2H), 2.53 (s, 3H), 2.40-2.29 (m, 9H), 2.21 (s, 3H), 1.57-1.52 (m, 8H).
1H NMR (400 MHz, CD3OD) δ 7.17 (d, J = 9.2 Hz, 2H), 7.25 (d, J = 8.8 Hz, 2H), 6.60 (s, 1H), 3.77 (s, 3H), 2.78 (s, 3H), 1.64 (s, 6H).
1H NMR (400 MHz, DMSO-d6) δ 9.26-8.43 (m, 2H), 7.12-7.04 (m, 2H), 6.80-6.74 (m, 2H), 6.67 (s, 1H), 3.66 (s, 3H), 1.54 (s, 6H).
1H NMR (400 MHz, CD3OD) δ 7.14 (d, J = 8.82 Hz, 2 H), 6.80 (d, J = 9.04 Hz, 2 H), 6.59 (s, 1 H), 3.74 (s, 3 H), 3.22 (t, J = 6.84 Hz, 2 H), 2.35-2.30 (m, 2 H), 2.21 (s, 6 H), 1.71-1.64 (m, 2 H), 1.62 (s, 6 H).
1H NMR (400 MHz, CD3OD) δ 7.14 (d, J = 8.8 Hz, 2H), 6.80 (d, J = 8.8 Hz, 2H), 6.59 (s, 1H), 3.74 (s, 3H) ,3.21 (br t, J = 6.7 Hz, 2H), 2.68-2.24 (m, 6H), 1.97-1.39 (m, 8H), 1.03 (t, J = 7.2 Hz, 6H).
1H NMR (400 MHz, CD3OD) δ 7.13 (d, J = 8.82 Hz, 2 H), 7.09-7.04 (m, 3 H), 6.79 (d, J = 8.82 Hz, 2 H), 6.62-6.55 (m, 4 H), 3.72 (s, 3 H), 3.25-3.19 (m, 2 H), 3.06 (br t, J = 6.50 Hz, 2 H), 1.61 (s, 6 H), 1.59- 1.54 (m, 4 H).
1H NMR (400 MHz, CDCl3) δ 7.16-7.14 (m, 2H), 6.84- 6.82 (m, 2H), 6.46 (s, 1H), 3.78 (s, 3H), 3.38-3.34 (m, 2H), 2.97-2.93 (m, 2H), 2.68-2.67 (m, 3H), 1.96- 1.89 (m, 2H), 1.63 (s, 6H).
1H NMR (400 MHz, CDCl3) δ 8.67 (br s, 1H), 7.13- 7.11 (m, 2H), 6.82-6.80 (m, 2H), 6.41 (s, 1H), 4.85 (br s, 1H), 3.77 (s, 3H), 3.67- 3.60 (m, 1H), 3.27-3.24 (m, 2H), 2.64-2.63 (m, 3H), 2.41-2.37 (m, 1H), 2.25-2.17 (m, 2H), 2.10- 2.05 (m, 2H), 1.61 (s, 6H).
1H NMR (400 MHz, CDCl3) δ 9.06 (br s, 1H), 7.12- 7.09 (m, 2H), 6.82-.679 (m, 2H), 6.44 (s, 1H), 4.94 (br s, 1H), 3.77 (s, 3H), 3.75- 3.64 (m, 1H), 3.31-3.28 (m, 2H), 2.68-2.67 (m, 3H), 2.51-2.47 (m, 1H), 2.43-2.36 (m, 2H), 1.99- 1.91 (m, 2H), 1.60 (s, 6H).
1H NMR (400 MHz, DMSO-d6) δ 10.72 (br, 1H), 9.10-8.70 (m, 2H), 7.09- 7.07 (m, 2H), 6.95-6.93 (m, 2H), 6.78-6.76 (m, 2H), 6.62 (s, 1H), 4.22-4.20 (m, 2H), 3.66 (s, 3H), 3.30- 3.25 (m, 4H), 3.20-3.14 (m, 4H), 1.53 (s, 6H).
1H NMR (400 MHz, DMSO-d6) δ 10.74 (br s, 2H), 7.27 (s, 1H), 7.13- 7.10 (m, 2H), 6.99-6.97 (m, 2H), 6.82-6.79 (m, 2H), 6.68 (s, 1H), 4.26- 4.24 (m, 2H), 3.70 (s, 3H), 3.47-3.40 (m, 4H), 3.28- 3.25 (m, 2H), 3.16-3.08 (m, 2H), 2.80-2.79 (m, 3H), 1.57 (s, 6H).
1H NMR (400 MHz, CDCl3) δ 7.84 (br, 1H), 7.44 (d, J = 8.4 Hz, 2H), 7.34 (d, J = 8.8 Hz, 2H), 7.28 (s, 1H), 6.80 (s, 1H), 4.72-4.68 (m, 1H), 4.29-4.25 (m, 2H), 3.95-3.91 (m, 2H), 2.58 (s, 1H), 1.93 (s, 3H).
1H NMR (400 MHz, CDCl3) δ 7.46 (d, J = 7.6 Hz, 2H), 7.37 (d, J = 8.4 Hz, 2H), 6.76 (s, 1H), 3.64 (t, J = 5.2 Hz, 2H), 3.43 (t, J = 6.0 Hz, 2H), 2.58 (s, 1H), 1.95 (s, 3H), 1.70-1.69 (m, 2H).
1H NMR (400 MHz, CDCl3) δ 7.48-7.42 (m, 4H), 7.00 (s, 1H), 4.11-4.08 (m, 2H), 3.82-3.67 (m, 2H), 3.66- 3.63 (m, 4H), 3.35 (s, 2H), 3.33-3.21 (m, 2H), 3.00 (s, 1H), 1.94 (s, 3H).
1H NMR (400 MHz, CD3OD) 7.44 (s, 4H), 6.91 (d, J = 1.0 Hz, 1H), 3.66-3.75 (m, 1H), 3.51 (d, J = 5.3 Hz, 2 H), 3.38-3.47 (m, 1H), 3.21 (ddd, J = 13.8, 6.9, 2.6 Hz, 1H), 2.95 (s, 1H), 1.92 ppm (s, 3H)
1H NMR R (400 MHz, CDCl3) δ 7.44-7.42 (m, 2 H), 7.37-7.35 (m, 2H), 6.81 (s, 1 H), 3.53-3.50 (m, 2 H), 3.38-3.35 (m, 2 H), 2.59 (s, 1 H), 2.38-2.29 (m, 1 H), 2.21-2.12 (m, 1 H), 0.94 (t, J = 7.6 Hz, 3 H)
1H NMR (400 MHz, DMSO-d6) δ 10.50 (s, 1 H), 7.47 (br d, J = 8.28 Hz, 2 H), 7.19 (br d, J = 8.28 Hz, 2 H), 6.66 (s, 1 H), 6.47 (br s, 1 H), 4.76 (br s, 1 H), 3.41 (br d, J = 5.27 Hz, 2 H), 3.16 (br d, J = 5.77 Hz, 2 H), 2.65 (br d, J = 13.30
1H NMR (400 MHz, CDCl3) δ 7.46 (d, J = 8.5 Hz, 2H), 7.36 (d, J = 8.5 Hz, 2H), 6.72 (s, 1H), 3.62 (br d, J = 4.3 Hz, 2H), 3.36 (br d, J = 3.9 Hz, 2H), 2.67 (s, 1H), 1.96 (s, 3H)
1H NMR (400 MHz, CDCl3) δ 7.41-7.39 (m, 2H), 7.31- 7.29 (m, 2H), 7.24 (s, 1H), 3.45-3.43 (m, 2H), 3.32- 3.29 (m, 2H), 2.52 (s, 1H), 1.89 (s, 3H).
1H NMR (400 MHz, CDCl3) δ 7.37-7.35 (m, 2H), 7.26- 7.24 (m, 2H), 7.19 (s, 1H), 6.69 (s, 1H), 3.38-3.37 (m, 2H), 3.25-3.24 (m, 2H), 2.47 (s, 1H), 1.84 (s, 3H).
1H NMR (400 MHz, DMSO-d6) δ 10.60 (s, 1H), 7.53-7.50 (m, 2H), 7.39- 7.37 (m, 2H), 6.90 (s, 1H), 3.50 (s, 1H), 1.85 (s, 3H).
1H NMR (400 MHz, DMSO-d6) δ 10.61 (s, 1H), 7.53-7.51 (m, 2H), 7.39- 7.34 (m, 2H), 5.76 (s, 3H), 3.50 (s, 1H), 1.85 (s, 3H).
1H NMR (400 MHz, DMSO-d6) δ 10.64 (s, 1H), 7.53-7.50 (m, 2H), 7.39- 7.37 (m, 2H), 6.89 (s, 1H), 3.50 (s, 1H), 1.85 (s, 3H).
1H NMR (400 MHz, CDCl3) δ 7.79 (br, 1H), 7.41-7.39 (m, 2H), 7.31-7.29 (m, 2H), 7.24 (s, 1H), 6.75 (s, 1H), 4.07 (t, J = 8.0 Hz, 2H), 3.83- 3.80 (m, 2H), 3.72-3.71 (m, 2H), 2.81-2.77 (m, 1H), 2.54 (s, 1H), 1.89 (s, 3H).
1H NMR (400 MHz, CDCl3) δ 7.85 (br, 1H), 7.46-7.43 (m, 2H), 7.36-7.33 (m, 2H), 6.79 (s, 1H), 4.11-4.08 (m, 2H), 3.88-3.85 (m, 2H), 3.76-3.75 (m, 2H), 2.87- 2.80 (m, 1H), 2.58 (s, 1H), 1.94 (s, 3H).
1H NMR (400 MHz, CDCl3) δ 7.85 (br, 1H), 7.45-7.43 (m, 2H), 7.36-7.33 (m, 2H), 6.79 (s, 1H), 4.11-4.09 (m, 2H), 3.87-3.85 (m, 2H), 3.77-3.75 (m, 2H), 2.85- 2.81 (m, 1H), 2.58 (s, 1H), 1.93 (s, 3H).
1H NMR (400 MHz, CDCl3) δ 7.38 (d, J = 8.8 Hz, 2H), 6.87-6.84 (m, 2H), 6.73 (s, 1H), 3.80 (s, 3H), 3.45 (s, 2H), 3.35-3.33 (m, 2H), 2.54 (s, 1H), 1.94 (s, 3H).
1H NMR (400 MHz, CDCl3) δ 7.36 (d, J = 8.8 Hz, 2H), 6.83 (d, J = 8.8 Hz, 2H), 6.70 (s, 1H), 3.78 (s, 3H), 3.46 (br d, J = 4.8 Hz, 2H), 3.32 (br d, J = 4.8 Hz, 2H), 2.52 (s, 1H), 1.92 (s, 3H)
1H NMR (400 MHz, CDCl3) δ 7.37 (d, J = 8.8 Hz, 2H), 6.84 (d, J = 8.8 Hz, 2H), 6.70 (s, 1H), 3.78 (s, 3H), 3.49 (br d, J = 5.3 Hz, 2H), 3.34 (br d, J = 5.3 Hz, 2H), 2.52 (s, 1H), 1.92 (s, 3H)
1H NMR (400 MHz, DMSO-d6) δ 10.58 (s, 1H), 7.33 (d, J = 8.8 Hz, 2H), 6.86 (d, J = 8.8 Hz, 2H), 6.81 (s, 1H), 6.22 (br s, 2H), 3.72 (s, 3H), 3.40 (s, 1H), 1.83 (s, 3H)
1H NMR (400 MHz, DMSO-d6) δ 10.58 (br s, 1H), 7.33 (d, J = 8.8 Hz, 2H), 6.86 (d, J = 8.8 Hz, 2H), 6.81 (s, 1H), 6.24 (br s, 1H), 3.72 (s, 3H), 3.41 (s, 1H), 1.83 (s, 3H)
1H NMR (400 MHz, DMSO-d6) δ 10.60 (br s, 1H), 7.33 (d, J = 8.8 Hz, 2H), 6.86 (d, J = 8.8 Hz, 2H), 6.80 (s, 1H), 6.23 (br s, 1H), 3.72 (s, 3H), 3.40 (s, 1H), 1.83 (s, 3H)
1H NMR (400 MHz, DMSO-d6) δ 10.64 (s, 1 H), 7.33-7.46 (m, 4 H), 6.90 (s, 1 H), 6.34 (br s, 1 H), 4.75 (t, J = 5.14 Hz, 1 H), 3.50 (s, 1 H), 3.41 (q, J = 5.52 Hz, 2 H), 3.16 (q, J = 5.52 Hz, 2 H), 1.85 (s, 3 H)
1H NMR (400 MHz, DMSO-d6) δ 10.63 (br s, 1 H), 7.33-7.48 (m, 4 H), 6.90 (s, 1H), 6.35 (br s, 1 H), 4.75 (t, J = 5.27 Hz, 1 H), 3.50 (s, 1 H), 3.41 (q, J = 5.35 Hz, 2H), 3.16 (q, J = 5.52 Hz, 2 H), 1.85 (s, 3 H)
1H NMR (400 MHz, DMSO-d6) δ 10.64 (br s, 1 H), 7.34-7.49 (m, 4 H), 6.90 (s, 1H), 6.35 (br s, 1 H), 4.76 (t, J = 5.14 Hz, 1 H), 3.51 (s, 1 H), 3.42 (q, J = 5.52 Hz, 2H), 3.16 (q, J = 5.35 Hz, 2 H), 1.85 (s, 3 H)
1H NMR (400 MHz, DMSO-d6) δ 10.76 (br s, 1 H), 9.25 (br s, 2 H), 7.43 (d, J = 8.56 Hz, 2 H), 7.34 (d, J = 1.96 Hz, 1 H), 7.24- 7.20 (m, 1 H), 7.15 (d, J = 8.56 Hz, 4 H), 6.74 (s, 1 H), 4.25 (br d, J = 5.62 Hz, 2 H), 3.27-3.08 (m, 8 H), 1.57 (s, 6 H).
1H NMR (400 MHz, DMSO-d6) δ 10.67 (br s, 1 H) 9.14 (br s, 2 H), 7.43 (d, J = 8.56 Hz, 2 H), 7.15 (d, J = 8.56 Hz, 2 H), 7.12 (br s, 1 H), 6.93-6.88 (m, 2 H), 6.80 (br d, J = 8.07 Hz, 1 H), 6.74 (s, 1 H), 4.25 (br d, J = 5.38 Hz, 2 H), 3.77 (s, 3 H), 3.18 (br d, J = 14.18 Hz, 8 H), 1.57 (s, 6 H).
1H NMR (400 MHz, DMSO-d6) δ 10.79 (br s, 1 H), 9.48 (br s, 2 H), 7.49 (br d, J = 8.80 Hz, 1 H), 7.43 (d, J = 8.56 Hz, 2 H), 7.15 (d, J = 8.56 Hz, 2 H), 7.03 (br d, J = 8.07 Hz, 1 H), 6.94 (s, 1 H), 6.81 (br d, J = 7.83 Hz, 1 H), 6.77 (s, 1 H), 6.01 (br s, 8 H), 4.61 (dt, J = 11.98, 5.99 Hz, 1 H), 4.24 (br d, J = 4.40 Hz, 2 H), 1.58 (s, 6 H), 1.28 (d, J = 6.11 Hz, 6 H).
1H NMR (400 MHz, DMSO-d6) δ 10.76 (br s, 1 H), 9.06 (br s, 1 H), 8.88 (br d, J = 9.78 Hz, 1 H), 7.43 (d, J = 8.56 Hz, 2 H), 7.29- 7.19 (m, 2 H), 7.15 (d, J = 8.56 Hz, 2 H), 7.10-7.04 (m, 2 H), 6.74 (s, 1 H), 4.28 (br d, J = 5.62 Hz, 2 H), 3.33 (br d, J = 12.47 Hz, 2 H), 3.34-2.93 (m, 2 H), 1.93-1.81 (m, 3 H), 1.57 (s, 6 H), 1.23 (br s, 2 H).
1H NMR (400 MHz, DMSO-d6) δ 9.50 (br s, 2 H), 8.23 (s, 1 H), 7.76- 7.57 (m, 1 H), 7.17-7.06 (m, 2 H), 6.86-6.79 (m, 2 H), 6.72 (s, 1 H), 4.26- 4.18 (m, 2 H), 4.0-3.92 (m, 4 H), 3.70 (s, 3 H), 3.13 (s, 4 H), 2.40 (s, 3 H), 1.57 (s, 6 H).
1H NMR (400 MHz, DMSO-d6) δ 10.73 (br s, 1 H), 8.93 (br, s, 1 H), 8.72 (br s, 1 H), 7.26-7.20 (m, 1 H), 7.16-7.02 (m, 5 H), 6.81 (d, J = 8.80 Hz, 2 H), 6.66 (s, 1 H), 4.29 (br d, J = 5.87 Hz, 2 H), 3.70 (s, 3 H), 3.34 (br d, J = 12.23 Hz, 2 H), 3.15-3.07 (m, 1 H), 3.07-2.94 (m, 2 H), 1.87 (br s, 4 H), 1.57 (s, 6 H).
1H NMR (400 MHz, CD3OD) δ 7.23-7.16 (m, 3 H), 7.11 (s, 1 H), 7.07 (s, 1 H), 6.97-6.87 (m, 3 H), 4.75 (dt, J = 11.49, 5.75 Hz, 1 H), 4.40 (s, 2 H), 3.76 (s, 3 H), 3.51 (s, 8 H), 1.69 (s, 6 H), 1.38 (d, J = 5.87 Hz, 6 H).
1H NMR (400 MHz, DMSO-d6) δ 11.30 (s, 1H) 10.94 (s, 1H) 8.64 (s, 1H) 8.55 (s, 1H) 7.09 (d, J = 8.82 Hz, 2H) 6.95 (s, 1H) 6.78 (d, J = 8.82 Hz, 2H) 6.64 (s, 1H) 4.00 (d, J = 13.89 Hz, 1H) 3.67 (s, 3H) 3.37-3.49 (m, 1H) 3.35 (s, 2H) 3.01- 3.23 (m ,5H) 2.06-2.28 (m, 1H) 1.92-2.06 (m, 1H) 1.75-
1H NMR (400 MHz, D2O) δ 7.20-7.13 (m, 2H), 6.95 (s, 1H), 6.89-6.83 (m, 2H), 4.20-3.74 (m, 3H), 3.71 (s, 3H), 3.68-3.47 (m, 4H), 3.46-3.32 (m, 2H), 2.65- 2.48 (m, 1H), 2.24-2.07 (m, 1H), 1.56 (s, 6H).
1H NMR (40 0MHz, DMSO-d6) δ 11.79 (br s, 1H), 10.68 (br s, 1H), 9.97 (br s, 2H), 7.12 (d, J = 8.6 Hz, 2H), 6.88 (s, 1H), 6.81 (d, J = 8.8 Hz, 2H), 6.67 (s, 1H), 3.75-3.62 (m, 6H), 3.58-3.49 (m, 1H), 3.48- 3.36 (m, 1H), 3.29-3.16 (m, 3H), 3.15-2.99 (m, 3H), 1.96-1.82 (m, 2H),
1H NMR (400 MHz, DMSO-d6) δ 8.47 (br s, 3 H), 7.24 (br s, 1 H), 7.12 (d, J = 8.82 Hz, 2 H), 6.82 (d, J = 8.60 Hz, 2 H), 6.70 (s, 1 H), 3.83 (br d, J = 5.07 Hz, 1 H), 3.70 (s, 3 H), 3.58 (br dd, J = 10.80, 6.62 Hz, 1 H), 3.52-3.43 (m, 1 H), 3.41- 3.28 (m, 3 H), 3.26-3.13 (m, 4 H), 2.22 (dq, J = 13.70, 6.90 Hz, 1 H), 2.05-1.92 (m, 1 H), 1.84 (dt, J = 14.55, 7.06 Hz, 2 H), 1.57 (s, 6 H).
1H NMR (400 MHz, DMSO-d6) δ 7.10-7.07 (m, 2 H), 6.78-6.75 (m, 2 H), 6.59 (s, 1 H), 3.67 (s, 3 H), 3.30-3.15 (m, 2 H), 3.02- 2.95 (m, 6 H), 2.68-2.66 (m, 4 H), 1.79-1.72 (m, 2 H), 1.52 (s, 6 H).
1H NMR (400 MHz, DMSO-d6) δ 10.75 (br s, 1 H), 9.33 (br s, 2 H), 7.39 (br s, 1 H), 7.16-7.10 (m, 3 H), 6.98 (dd, J = 11.36, 7.39 Hz, 1 H), 6.80 (d, J = 8.82 Hz, 2 H), 6.68 (s, 1 H), 4.27 (br d, J = 5.51 Hz, 2 H), 3.70 (s, 3 H), 3.23 (br s, 8 H), 1.57 (s, 6 H).
1H NMR (400 MHz, DMSO-d6) δ 10.85-10.72 (m, 1H), 9.80-9.68 (m, 1H), 8.16-8.08 (m, 1H), 7.12 (br d, J = 8.8 Hz, 2H), 7.05-6.93 (m, 2H), 6.86- 6.76 (m, 2H), 6.71-6.64 (m, 1H), 4.27 (br d, J = 6.1 Hz, 4H), 3.88 (s, 2H), 3.70 (s, 3H), 3.54-3.49 (m, 2H), 2.86-2.76 (m, 1H), 2.14- 2.06 (m, 1H), 1.57 (s, 6H).
1H NMR (400 MHz, DMSO-d6) δ 9.25 (br s, 2H), 7.33 (s, 0.4H), 7.25- 7.23 (m, 2H), 7.20-7.18 (m, 2H), 7.14-7.12 (m, 0.4 H), 6.98-6.96 (m, 2H), 6.82- 6.80 (m, 2H), 6.66 (s, 1H), 4.38-4.36 (m, 2H), 3.94- 3.91 (m, 2H), 3.76-3.72 (m, 1H), 3.72 (s, 3H), 3.39- 3.38 (m, 4H), 3.37-3.20 (m, 4H), 1.60 (s, 6H).
1H NMR (400 MHz, CD3OD) δ 7.34 (d, J = 8.56 Hz, 2 H) 7.21 (d, J = 8.56 Hz, 2 H) 7.08-7.00 (m, 3 H) 6.68 (s, 1H) 4.59 (br d, J = 16.63 Hz, 1 H) 4.40 (t, J = 8.56 Hz, 2 H) 3.98 (dd, J = 8.31, 6.11 Hz, 2 H) 3.77- 3.87 (m, 1 H) 3.02 (br d, J = 6.11 Hz, 8 H) 2.43-2.53 (m, 2 H) 2.01-2.13 (m, 2 H) 1.62-1.77 (m, 4 H)
1H NMR (400 MHz, DMSO-d6) δ 10.93 (s, 1 H) 9.22 (s, 2 H) 7.47 (d, J = 8.4 Hz, 2 H) 7.30 (d, J = 8.4 Hz, 2 H) 7.21 (d, J = 8.4 Hz, 2 H), 6.90-6.98 (m, 3 H), 4.30 (br s, 1 H), 3.87-3.84 (m, 2 H), 3.66-3.74 (m, 1 H), 3.46 (s, 1 H), 3.31- 3.30 (m, 4 H), 3.22-3.10 (m, 4 H), 1.82 (s, 3 H)
1H NMR (400 MHz, CD3OD) δ 7.53-7.20 (m, 2 H), 7.44-7.42 (m, 2 H), 7.14 (s, 1 H), 3.33-3.27 (m, 2 H), 3.26-3.25 (m, 4 H), 3.16 (s, 1 H), 1.95 (s, 3 H), 1.79-1.77 (m, 4 H)
1H NMR (400 MHz, CD3OD) δ 7.47-7.54 (m, 2H), 7.38-7.46 (m, 2H), 7.14 (s, 1H), 3.62-3.82 (m, 8H), 3.47 (br t, J = 5.6 Hz, 2H), 3.14 (s, 1H), 1.95 (s, 3H)
1H NMR (400 MHz, CDCl3) δ 7.44-7.26 (m, 4 H), 6.75 (s, 2 H), 5.82 (s, 2 H), 3.80-3.65 (m, 2 H), 3.25-3.13 (m, 2 H), 2.63 (s, 1 H), 1.92 (s, 3 H).
1H NMR (400 MHz, CDCl3) δ 9.63 (br. s, 1 H), 7.39-7.35 (m, 2 H), 7.25- 7.19 (m, 2 H), 6.65 (s, 2 H), 3.72-3.62 (m, 1 H), 3.52-3.33 (m, 2 H), 3.29- 3.09 (m, 2 H), 2.56 (s, 1 H), 1.86 (s, 3 H).
1H NMR (400 MHz, DMSO-d6) δ 10.95 (s, 1 H), 8.97 (br s, 2 H), 7.35-7.42 (m, 4 H), 7.20-7.30 (m, 1 H), 7.11-7.18 (m, 1 H), 7.04-7.09 (m, 1 H), 6.97 (s, 1 H), 4.33 (br t, J = 8.11 Hz, 2 H), 3.91 (br t, J = 7.03 Hz, 2 H), 3.75-3.81 (m, 1 H), 3.48 (s, 1 H), 3.21 (br d, J = 8.94 Hz, 8 H), 1.85 (s, 3 H)
1H NMR (400 MHz, DMSO-d6) δ 10.95 (s, 1 H), 8.95 (br s, 2 H), 7.35-7.42 (m, 4 H), 7.18-7.30 (m, 1 H), 7.10-7.17 (m, 1 H), 7.02-7.09 (m, 1 H), 6.97 (s, 1 H), 4.33 (br t, J = 8.17 Hz, 2 H), 3.86-3.97 (m, 2 H), 3.75-3.81 (m, 1 H), 3.48 (s, 1 H), 3.23 (br s, 4 H), 3.20 (br s, 4 H), 1.86 (s, 3H)
1H NMR (400 MHz, DMSO-d6) δ 10.92 (1, 1H), 7.38-7.36 (m, 4H), 6.49 (s, 1H), 4.80 (s, 1H), 3.58 (s, 1H), 3.45-3.35 (m, 2H), 3.22-3.18 (m, 2H), 1.85 (s, 3H)
1H NMR (400 MHz, DMSO-d6) δ 10.92 (1, 1H), 7.40-7.30 (m, 4H), 6.50 (s, 1H), 4.77 (s, 1H), 3.55 (s, 1H), 3.43-3.35 (m, 2H), 3.20-3.15 (m, 2H), 1.87 (s, 3H)
1H NMR (400 MHz, DMSO-d6) δ 10.66 (s, 1H), 7.40-7.46 (m, 2H), 7.33- 7.39 (m, 2H), 6.88 (s, 1H), 6.27 (s, 1H), 4.32 (s, 1H), 3.48 (s, 1H), 3.13-3.23 (m, 2H), 1.85 (s, 3H), 1.45-1.57 (m, 2H), 1.09 (s, 6H)
1H NMR (400 MHz, DMSO-d6) δ 10.65 (s, 1H), 7.41-7.46 (m, 2H), 7.34- 7.40 (m, 2H), 6.88 (s, 1H), 6.26 (s, 1H), 4.31 (s, 1H), 3.49 (s, 1H), 3.13-3.22 (m, 2H), 1.85 (s, 3H), 1.46-1.56 (m, 2H), 1.09 (s, 6H)
1H NMR (400 MHz, DMSO-d6) δ 10.59 (1, 1H), 7.44-7.42 (m, 2H), 7.38- 7.36 (m, 2H), 6.89 (s, 1H), 6.22 (s, 1H), 3.48 (s, 1H), 1.85 (s, 3H)
1H NMR (400 MHz, DMSO-d6) δ 10.60 (1, 1H), 7.44-7.42 (m, 2H), 7.39- 7.36 (m, 2H), 6.90 (s, 1H), 6.22 (s, 1H), 3.49 (s, 1H), 1.85 (s, 3H)
1H NMR (400 MHz, DMSO-d6) δ 7.36 (4H, J = 19.6 Hz, t), 6.91 (1H, s), 3.51 (4H, s), 3.45 (1H, s), 3.40 (4H, s), 1.83 (3H, s)
1H NMR (400 MHz, DMSO-d6) δ 7.38-7.33 (4H, m), 6.90 (1H, s) ,3.47 (2H, J = 10.4 Hz, t), 3.44 (1H, s), 3.37 (2H, J = 10.4 Hz, t), 2.91 (3H, s), 1.82 (3H, s)
1H NMR (400 MHz, DMSO-d6) δ 10.83 (s, 1 H), 7.29 (d, J = 8.78 Hz, 2 H), 6.87 (s, 1 H), 6.85 (s, 2 H), 4.78 (t, J = 5.27 Hz, 1 H), 3.94 (br s, 2 H), 3.71 (s, 3 H), 3.68 (br s, 2 H), 3.48 (t, J = 5.65 Hz, 2 H), 3.38 (s, 1 H), 2.56-2.70 (m, 1 H), 1.83 (s, 3 H).
1H NMR (400 MHz, DMSO-d6) δ 10.85 (s, 1 H), 7.30 (br d, J = 8.78 Hz, 2 H), 6.87 (s, 1 H), 6.86 (s, 2 H), 4.79 (t, J = 5.14 Hz, 1 H), 3.86-4.07 (m, 2 H), 3.72 (s, 3 H), 3.69 (br s, 2 H), 3.49 (br t, J = 5.52 Hz, 2 H), 3.39 (s, 1 H), 2.56- 2.72 (m, 1 H), 1.84 (s, 3 H).
1H NMR (400 MHz, CDCl3) δ 7.79 (s, 1 H), 7.45-7.40 (m, 2 H), 7.30- 7.20 (m, 2 H), 6.78 (s, 1 H), 4.20-4.08 (m, 2 H), 3.90- 3.84 (m, 2 H), 3.80-3.75 (m, 2 H), 2.88-2.75 (m, 1 H), 2.57 (s, 1 H), 2.10- 2.00 (m, 1 H), 1.92 (s, 3 H).
1H NMR (400 MHz, CDCl3) δ 7.78 (s, 1 H), 7.45- 7.36 (m, 2 H), 7.30-7.20 (m, 2 H), 6.78 (s, 1 H), 4.20- 4.08 (m, 2 H), 3.90-3.84 (m, 2 H), 3.80-3.75 (m, 2 H), 2.90-2.80 (m, 1 H), 2.57 (s, 1 H), 2.05-1.95 (m, 1 H), 1.93 (s, 3 H).
1H NMR (400 MHz, DMSO-d6) δ 8.23 (s, 1H), 7.41-7.35 (m, 4H), 6.99- 6.91 (m, 2H), 6.75 (d, J = 7.7 Hz, 1H), 6.67 (s, 1H), 4.47 (s, 2H), 3.63 (s, 2H), 3.05 (s, 4H), 2.90 (s, 4H), 2.70 (s, 2H), 1.81 (s, 3H).
1H NMR (400 MHz, DMSO-d6) δ 7.34 (t, J = 20.0 Hz, 4H), 6.87 (s, 1H), 3.44-3.40 (m, J = 16.0, 5H), 2.88 (s, 3H), 1.79 (s, 3H).
1H NMR (400 MHz, DMSO-d6) δ 7.34 (t, J = 20.0 Hz, 4H), 6.86 (s, 1H), 3.46-3.40 (m, J = 16.0, 9H), 1.78 (s, 3H).
1H NMR (400 MHz, DMSO-d6) δ 7.43-7.34 (dd, J = 27.8, 7.5 Hz, 4H), 6.87 (s, 1H), 6.38 (s, 1H), 4.56 (s, 1H), 3.02 (d, J = 4.0 Hz, 2H), 1.83 (s, 3H), 1.03 (s, 6H).
1H NMR (400 MHz, DMSO-d6) δ 7.36 (s, 4H), 6.90 (s, 1H), 4.93 (s, 1H), 4.22 (s, 1H), 3.44 (s, 4H), 1.83 (s, 3H), 1.74 (s, 2H).
1H NMR (400 MHz, DMSO-d6) δ 7.36 (s, 4H), 6.90 (s, 1H), 4.68 (s, 1H), 3.44 (s, 4H), 3.11 (s, 2H), 2.24 (s, 1H), 1.83 (s, 3H), 1.60 (s, 2H).
1H NMR (400 MHz, DMSO-d6) δ 7.40-7.36 (m, J = 16.0 Hz, 4H), 6.94 (s, 1H), 3.47 (s, 1H), 1.84 (s, 3H).
1H NMR (400 MHz, DMSO-d6) δ 7.31 (s, 4H), 7.13-7.09 (m, 4H), 6.83 (d, J = 8.0 Hz, 1H), 3.54 (s,, 2H), 3.50 (m, 4H), 2.78 (s, 4H), 1.84 (s, 3H).
1H NMR (400 MHz, DMSO-d6) δ 7.41-7.34 (m, 4H), 6.86 (s, 1H), 3.16 (s, 4H), 2.67 (s, 1H), 1.82 (s, 3H), 1.66 (s, 2H), 1.49 (s, 1H), 1.25 (s, 2H), 1.01 (s, 3H).
1H NMR (400 MHz, DMSO-d6) δ 10.77-11.73 (m, 1 H), 8.01 (br s, 1 H), 7.39-7.44 (m, 2 H), 7.34- 7.39 (m, 2 H), 7.02 (d, J = 8.70 Hz, 2 H), 6.86 (s, 1 H), 6.80 (br d, J = 8.82 Hz, 2 H), 3.48 (s, 1 H), 2.92- 2.99 (m, 4 H), 2.75-2.83 (m, 4 H), 1.84 (s, 3 H), 1.06 (br d, J = 9.06 Hz, 4 H).
1H NMR (400 MHz, DMSO-d6) δ 10.50 (br s, 1 H), 7.40-7.47 (m, 2 H), 7.34-7.40 (m, 2 H), 7.02 (br, d, J = 8.70 Hz, 3 H), 6.91 (s, 1 H), 6.82 (br d, J = 8.82 Hz, 2 H), 3.50 (s, 1 H), 2.92-3.04 (m, 4 H), 2.75- 2.88 (m, 4 H), 1.84 (s, 3 H), 1.09 (br d, J = 3.58 Hz, 4 H).
1H NMR (400 MHz, DMSO-d6) δ 12.00 (br s, 1 H), 11.01 (br s, 1 H), 9.79 (br s, 2 H), 7.40 (dd, J = 8.66, 5.40 Hz, 2 H), 7.13 (t, J = 8.66 Hz, 2 H), 6.93 (s, 1 H), 4.09 (br s, 2 H), 3.76- 3.85 (m, 2 H), 3.57 (br d, J = 4.77 Hz, 2 H), 3.39-3.53 (m, 7 H), 3.26 (br s, 2 H), 3.11 (br d, J = 6.53 Hz, 1 H), 1.85 (s, 3 H).
1H NMR (400 MHz, DMSO-d6) δ 12.01 (br s, 1 H), 11.01 (br s, 1 H), 9.79 (br s, 2 H), 7.40 (dd, J = 8.41, 5.40 Hz, 2 H), 7.13 (t, J = 8.78 Hz, 2 H), 6.93 (s, 1 H), 4.01-4.12 (m, 2 H), 3.75-3.85 (m, 2 H), 3.58 (br s, 2 H), 3.37-3.52 (m, 7 H), 3.27 (br s, 2 H), 3.10 (br s, 1 H), 1.85 (s, 3 H).
1H NMR (400 MHz, DMSO-d6) δ 10.60 (br s, 1 H), 7.51 (d, J = 8.53 Hz, 2 H), 7.37 (d, J = 8.53 Hz, 2 H), 6.90 (s, 1 H), 6.33 (br s, 1 H), 4.86 (br d, J = 4.77 Hz, 1H), 4.59 (t, J = 5.65 Hz, 1 H), 3.50 (s, 1 H), 3.42- 3.49 (m, 1 H), 3.34-3.37 (m, 0.5 H), 3.20-3.31 (m, 2.5 H), 2.90-3.04 (m, 1 H), 1.85 (s, 3 H).
1H NMR (400 MHz, DMSO-d6) δ 10.62 (br s, 1 H), 7.51 (d, J = 8.53 Hz, 2 H), 7.37 (d, J = 8.53 Hz, 2 H), 6.89 (s, 1 H), 6.34 (br s, 1 H), 4.86 (br d, J = 4.52 Hz, 1 H), 4.60 (t, J = 5.40 Hz, 1 H), 3.50 (s, 1 H), 3.47 (br d, J = 4.77 Hz, 1 H), 3.35 (br s, 0.5 H), 3.20- 3.31 (m, 2.5 H), 2.90-3.03 (m, 1 H), 1.84 (s, 3 H).
1H NMR (400 MHz, DMSO-d6) δ 10.65 (s, 1 H), 7.50-7.35 (m, 4H), 6.34 (br. s, 1H), 4.76 (t, J = 4.0 Hz, 1H), 3.53 (s, 1 H), 3.41 (q, J = 4.0 Hz, 1H), 3.15 (q, J = 4.0 Hz, 1H), 1.86 (s, 3 H).
1H NMR (400 MHz, DMSO-d6) δ 7.44-7.35 (m, 4 H), 7.01-6.94 (m, 2 H), 6.81-6.75 (m, 1 H), 6.72- 6.68 (m, 1 H), 4.53 (s, 2H), 3.66 (t, J = 84 Hz, 2H), 3.50 (s, 1H), 3.05-2.99 (m, 4H), 2.88-2.82 (m, 4H), 2.75 (t, J = 8 Hz, 2H), 1.87 (s, 3H).
1H NMR (400 MHz, DMSO-d6) δ 7.44-7.36 (m, 4 H), 7.01-6.94 (m, 2 H), 6.80-6.75 (m, 1 H), 6.71- 6.68 (m, 1 H), 4.53 (s, 2H), 3.66 (t, J = 8 Hz, 2H), 3.50 (s, 1H), 3.04-2.98 (m, 4H), 2.86-2.80 (m, 4H), 2.75 (t, J = 8 Hz, 2H), 1.87 (s, 3H).
1H NMR (400 MHz, DMSO-d6) δ 10.63 (s, 1 H), 7.44 (dd, J = 8.78, 5.52 Hz, 2 H), 7.13 (t, J = 8.91 Hz, 2 H), 6.87 (s, 1 H), 6.34 (br s, 1 H), 4.75 (t, J = 5.02 Hz, 1 H), 3.48 (s, 1 H), 3.41 (q, J = 5.52 Hz, 2 H), 3.16 (q, J = 5.60 Hz, 2 H), 1.85 (s, 3
1H NMR (400 MHz, DMSO-d6) δ 10.63 (s, 1 H), 7.44 (dd, J = 8.78, 5.52 Hz, 2 H), 7.13 (t, J = 8.91 Hz, 2 H), 6.88 (s, 1 H), 6.33 (br s, 1 H), 4.75 (t, J = 5.14 Hz, 1 H), 3.48 (s, 1 H), 3.41 (q, J = 5.35 Hz, 2 H), 3.16 (q, J =
1H NMR (400 MHz, DMSO-d6) δ 10.94 (br s, 1 H), 7.44 (dd, J = 8.78, 5.52 Hz, 2 H), 7.13 (t, J = 8.91 Hz, 2 H), 6.92 (s, 2 H), 6.90 (s, 1 H), 6.48 (br t, J = 5.65 Hz, 1 H), 3.49- 3.56 (m, 2 H), 3.48 (s, 1 H), 3.13 (t, J = 6.65 Hz, 2 H), 1.85 (s, 3 H).
1H NMR (400 MHz, DMSO-d6) δ 10.95 (br s, 1 H), 7.37-7.50 (m, 2 H), 7.13 (t, J = 8.78 Hz, 2 H), 6.92 (s, 2 H), 6.90 (s, 1 H), 6.48 (br t, J = 5.90 Hz, 1 H), 3.49-3.56 (m, 2 H), 3.48 (s, 1 H), 3.14 (t, J = 6.65 Hz, 2 H), 1.85 (s, 3 H).
1H NMR (400 MHz, DMSO-d6) δ 10.75 (br s, 1 H), 9.17 (br s, 1 H), 8.99 (br s, 1 H), 7.46- 7.41 (m, 2 H), 7.40-7.36 (m, 2 H), 6.93 (s, 1 H), 6.82 (br s, 1 H), 3.75- 3.90 (m, 5 H), 3.52 (s, 1 H), 3.43 (d, J = 6.0 Hz, 2 H), 1.85 (s, 3 H)
1H NMR (400 MHz, DMSO-d6) δ 10.75 (br s, 1 H), 9.10 (br s, 1 H), 8.95 (br s, 1 H), 7.45- 7.41 (m, 2 H), 7.40-7.35 (m, 2 H), 6.93 (s, 1 H), 6.77 (br s, 1 H), 3.86 (br s, 5 H), 3.51 (s, 1 H) 3.43 (br d, J = 6.0 Hz, 2 H), 1.85 (s, 3 H)
1H NMR (400 MHz, DMSO-d6) δ 10.65 (s, 1 H), 7.50-7.35 (m, 4H), 6.34 (br. s, 1H), 4.76 (t, J = 4.0 Hz, 1H), 3.53 (s, 1 H), 3.41 (q, J = 4.0 Hz, 1H), 3.15 (q, J = 4.0 Hz, 1H), 1.86 (s, 3 H).
1H NMR (400 MHz, DMSO-d6) δ 7.46-7.34 (m, 4 H), 6.94 (s, 1H), 4.10- 3.95 (m, 2 H), 4.0 (br. s, 2H), 3.58 (br. s, 2H), 3.49 (br. s, 1 H), 2.81-2.70 (m, 1H), 2.64 (br. s, 4 H), 2.46- 2.40 (m, 3H), 2.24 (br. s, 4 H), 1.85 (s, 3 H).
1H NMR (400 MHz, DMSO-d6) δ 10.91 (br. s, 1H), 8.78 (br. s, 1H), 7.42- 7.35 (m, 4 H), 6.95 (s, 1H), 4.09-3.96 (m, 2 H), 3.65- 3.55 (br. s, 2H), 3.50 (br. s, 1 H), 3.08-2.99 (m, 4H), 2.87-2.70 (m, 1H), 2.60- 2.52 (m, 4 H), 1.85 (s, 3 H).
1H NMR (400 MHz, DMSO-d6) δ 10.47 (s, 1 H), 7.29-7.49 (m, 4 H), 6.88 (s, 1 H), 6.15 (br. s, 1 H), 4.93 (t, J = 5.40 Hz, 1 H), 3.49 (s, 1 H), 3.33 (br s, 2 H), 1.84 (s, 3 H), 1.19 (s, 6 H).
1H NMR (400 MHz, DMSO-d6) δ 10.47 (s, 1 H), 7.31-7.50 (m, 4 H), 6.88 (s, 1 H), 6.15 (br s, 1 H), 4.94 (t, J = 5.52 Hz, 1 H), 3.49 (s, 1 H), 3.33 (br s, 2 H), 1.84 (s, 3 H), 1.19 (s, 6 H).
1H NMR (400 MHz, DMSO-d6) δ 10.46 (br s, 1 H), 7.33-7.47 (m, 4 H), 6.91 (s, 1 H), 6.57 (br s, 1 H), 4.58-4.99 (m, 1 H), 3.49 (s, 1 H), 3.37 (br s, 2 H), 1.84 (s, 3 H), 0.54- 0.75 (m, 4 H).
1H NMR (400 MHz, DMSO-d6) δ 10.56 (br s, 1 H), 7.31-7.45 (m, 4 H), 6.92 (s, 1 H), 6.55 (br s, 1 H), 4.77 (br s, 1 H), 3.49 (s, 1 H), 3.36-3.37 (m, 2 H), 1.84 (s, 3 H), 0.53-0.77 (m, 4 H).
1H NMR (400 MHz, CDCl3) δ 7.42 (d, J = 8.3 Hz, 2H), 7.31-7.27 (m, 2H), 6.76 (s, 1H), 3.87 (s, 1H), 3.71- 3.52 (m, 4H), 2.60 (s, 1H), 1.93 (s, 3H)
1H NMR (400 MHz, CDCl3) δ 7.41 (d, J = 8.3 Hz, 2H), 7.32-7.26 (m, 2H), 6.75 (s, 1H), 3.86 (s, 1H), 3.69- 3.52 (m, 4H), 2.60 (s, 1H), 1.92 (s, 3H)
1H NMR (400 MHz, CDCl3) δ 7.44-7.36 (m, 2H), 7.31- 7.27 (m, 2H), 6.77 (s, 1H), 3.52-3.41 (m, 2H), 3.39- 3.27 (m, 2H), 2.56 (s, 1H), 1.93 (s, 3H)
1H NMR (400 MHz, CDCl3) δ 7.43-7.36 (m, 2H), 7.29 (d, J = 7.3 Hz, 2H), 6.77 (s, 1H), 3.53-3.41 (m, 2H), 3.38-3.27 (m, 2H), 2.56 (s, 1H), 1.93 (s, 3H)
1H NMR (400 MHz, DMSO-d6) δ 10.64 (br s, 1H), 7.47-7.40 (m, 2H), 7.40-7.34 (m, 2H), 6.89 (s, 1H), 6.41 (s, 1H), 3.54- 3.42 (m, 2H), 3.37-3.20 (m, 3H), 3.04-2.91 (m, 1H), 1.85 (s, 3H)
1H NMR (400 MHz, DMSO-d6) δ 10.64 (br s, 1H), 7.46-7.40 (m, 2H), 7.40-7.34 (m, 2H), 6.89 (s, 1H), 6.43 (s, 1H), 3.54- 3.43 (m, 2H), 3.37-3.20 (m, 3H), 3.03-2.91 (m, 1H), 1.85 (s, 3H)
1H NMR (400 MHz, DMSO-d6) δ 10.64 (br s, 1H), 7.48-7.40 (m, 2H), 7.40-7.33 (m, 2H), 6.89 (s, 1H), 6.43 (s, 1H), 3.56- 3.41 (m, 2H), 3.37-3.19 (m, 3H), 3.04-2.88 (m, 1H), 1.85 (s, 3H)
1H NMR (400 MHz, DMSO-d6) δ 10.67 (br s, 1H), 7.48-7.40 (m, 2H), 7.40-7.33 (m, 2H), 6.90 (s, 1H), 6.54 (s, 1H), 3.57- 3.42 (m, 2H), 3.38-3.20 (m, 3H), 3.07-2.90 (m, 1H), 1.85 (s, 3H)
1H NMR (400 MHz, DMSO-d6) δ 10.57 (br. s, 1H), 7.51 (d, J = 8.5 Hz, 2H), 7.38 (d, J = 8.6 Hz, 2H), 6.89 (s, 1H), 6.37 (br. s, 1H), 4.54 (s, 1H), 3.50 (s, 1H), 3.04 (d, J = 5.7 Hz, 2H), 1.85 (s, 3H), 1.05 (s, 6H).
1H NMR (400 MHz, DMSO-d6) δ 10.57 (br. s, 1H), 7.51 (d, J = 8.6 Hz, 2H), 7.38 (d, J = 8.6 Hz, 2H), 6.89 (s, 1H), 6.37 (br. s, 1H), 4.54 (s, 1H), 3.50 (s, 1H), 3.04 (d, J = 5.7 Hz, 2H), 1.85 (s, 3H), 1.05 (s, 6H).
1H NMR (400 MHz, DMSO-d6) δ 10.44 (br s, 1H), 7.48-7.33 (m, 4H), 7.23-7.06 (m, 4H), 6.90 (s, 1H), 6.51 (br s, 1H), 4.10 (br s, 1H), 3.60- 3.43 (m, 3H), 2.74-2.59 (m, 1H), 2.56-2.51 (m, 1H), 2.38-2.21 (m, 5H), 2.20-2.08 (m, 1H), 1.84 (s, 3H), 1.54-1.40 (m, 1H).
1H NMR (400 MHz, CDCl3) δ 7.32-7.27 (m, 2H), 6.89-6.79 (m, 2H), 6.74 (s, 1H), 6.02 (br s, 3H), 3.80 (s, 3H), 3.74- 3.59 (m, 2H), 3.15-2.95 (m, 2H), 2.54 (s, 1H), 1.87 (s, 3H).
1H NMR (400 MHz, CDCl3) δ 7.27-7.23 (m, 2H), 6.88-6.80 (m, 2H), 6.75 (s, 1H), 6.07 (br s, 3H), 3.80 (s, 3H), 3.74- 3.62 (m, 2H), 3.10-2.93 (m, 2H), 2.51 (s, 1H), 1.86 (s, 3H).
1H NMR (400 MHz, CD3OD) δ 7.54-7.46 (m, 2H), 7.32-7.25 (m, 2H), 6.91 (s, 1H), 3.93-3.76 (m, 1H), 3.60-3.41 (m, 2H), 2.96 (s, 1H), 1.92 (s, 3H), 1.16 (d, J = 6.4 Hz, 3H).
1H NMR (400 MHz, CD3OD) δ 7.55-7.43 (m, 2H), 7.37-7.24 (m, 2H), 6.90 (s, 1H), 3.91-3.76 (m, 1H), 3.56-3.44 (m, 2H), 2.96 (s, 1H), 1.92 (s, 3H), 1.16 (d, J = 6.4 Hz, 3H).
1H NMR (400 MHz, CD3OD) δ 7.58-7.39 (m, 2H), 7.36-7.18 (m, 2H), 6.90 (s, 1H), 3.97-3.75 (m, 1H), 3.62-3.37 (m, 2H), 2.96 (s, 1H), 1.92 (s, 3H), 1.16 (d, J = 6.4 Hz, 3H).
1H NMR (400 MHz, CD3OD) δ 7.57-7.46 (m, 2H), 7.35-7.21 (m, 2H), 6.91 (s, 1H), 4.00-3.73 (m, 1H), 3.56-3.41 (m, 2H), 2.96 (m, 1H), 1.92 (s, 3H), 1.16 (d, J = 6.4 Hz, 3H).
1H NMR (400 MHz, CD3OD) δ 7.54-7.44 (m, 2H), 7.32-7.25 (m, 2H), 6.91 (s, 1H), 3.90-3.76 (m, 1H), 3.28 (s, 1H), 3.16-3.04 (m, 1H), 2.95 (s, 1H), 1.92 (s, 3H), 1.15 (d, J = 6.4 Hz, 3H).
1H NMR (400 MHz, CD3OD) δ 7.52-7.44 (m, 2H), 7.32-7.26 (m, 2H), 6.91 (s, 1H), 3.89-3.78 (m, 1H), 3.30-3.25 (m, 1H), 3.15-3.06 (m, 1H), 2.95 (s, 1H), 1.92 (s, 3H), 1.15 (d, J = 6.4 Hz, 3H).
1H NMR (400 MHz, CD3OD) δ 7.56-7.43 (m, 2H), 7.34-7.22 (m, 2H), 6.91 (s, 1H), 3.92-3.70 (m, 1H), 3.30-3.25 (m, 1H), 3.15-3.06 (m, 1H), 2.95 (s, 1H), 1.92 (s, 3H), 1.15 (d, J = 6.4 Hz, 3H).
1H NMR (400 MHz, CD3OD) δ 7.59-7.43 (m, 2H), 7.35-7.14 (m, 2H), 6.91 (s, 1H), 3.89-3.75 (m, 1H), 3.30-3.24 (m, 1H), 3.14-3.05 (m, 1H), 2.95 (s, 1H), 1.92 (s, 3H), 1.15 (d, J = 6.4 Hz, 3H).
1H NMR (400 MHz, CDCl3) δ 7.34-7.28 (m, 2H), 7.22-7.19 (m, 2H), 6.69 (s, 1H), 3.23 (d, J = 5.5 Hz, 2H), 2.48 (s, 1H), 1.84 (s, 3H)
1H NMR (400 MHz, CDCl3) δ 7.43-7.35 (m, 2H), 7.31-7.27 (m, 2H), 6.76 (s, 1H), 3.31 (d, J = 5.5 Hz, 2H), 2.55 (s, 1H), 1.92 (s, 3H)
To a solution of tert-butyl 4-(4-((3-(4-(1-(4-bromophenyl)vinyl)thiazol-2-yl)ureido)methyl)phenyl)piperazine-1-carboxylate (120 mg) in MeOH (5 mL) was added Pd/C (12 mg), the mixture was stirred overnight at RT under hydrogen pressure. After filtration and evaporation, the obtained residue was purified by column chromatography on a silica gel to afford tert-butyl 4-(4-((3-(4-(1-(4-bromophenyl)ethyl)thiazol-2-yl)ureido)methyl)phenyl)piperazine-1-carboxylate (73 mg).
A suspension of 1-(4-(2-(4-bromophenyl)propan-2-yl)thiazol-2-yl)-3-((6-chloro-5-fluoropyridin-3-yl)methyl)urea (174 mg, 0.4 mmol), tert-butyl piperazine-1-carboxylate (82 mg, 0.44 mmol), X-phos (39 mg, 0.08 mmol), Pd2 (dba) 3 (36.6 mg, 0.04 mmol) and t-BuONa (46.1 mg, 0.48 mmol) in toluene (5 mL) was stirred at 90° C. under N2 atmosphere overnight. The reaction mixture was cooled to RT and filtered off the solid, the residue was dissolved in ethyl acetate (100 mL) and washed with brine. The organic phase was dried over MgSO4, filtered, concentrated in vacuum to give the crude product, which was purified by flashed column to give the desired product (67 mg, yield 25%).
Step 1 Preparation of 2-(4-(tert-butoxycarbonyl)-3-methylpiperazin-1-yl)-5-((3-(4-(2-(4-methoxyphenyl)propan-2-yl)thiazol-2-yl)ureido)methyl)benzoic acid
A mixture of tert-butyl 4-(2-(methoxycarbonyl)-4-((3-(4-(2-(4-methoxyphenyl)propan-2-yl)thiazol-2-yl)ureido)methyl)phenyl)-2-methylpiperazine-1-carboxylate (270 mg, 0.42 mmol, 1 eq) and KOH (23.5 mg, 0.42 mmol, 1 eq), was heated to reflux for 0.5 h. After cooling, the reaction was quenched with sat. NH4Cl (aq), extracted with EA, washed with brine, dried over Na2SO4, filtered and evaporated to dryness. The resulting residue was purified by Prep-TLC to give the desired compound (215 mg).
Step 2: Preparation of tert-butyl 4-(2-carbamoyl-4-((3-(4-(2-(4-methoxyphenyl)propan-2-yl)thiazol-2-yl)ureido)methyl)phenyl)-2-methylpiperazine-1-carboxylate
A mixture of 2-(4-(tert-butoxycarbonyl)-3-methylpiperazin-1-yl)-5-((3-(4-(2-(4-methoxyphenyl)propan-2-yl)thiazol-2-yl)ureido)methyl)benzoic acid (215 mg, 0.34 mmol, 1 eq), EDCI (132 mg, 0.69 mmol, 2 eq), HOBt (93 mg, 0.69 mmol, 2 eq) and DIEA (133 mg, 1.03 mmol, 3 eq) were dissolved in THF (0.1 M) and stirred for 15 min at RT. NH4Cl (36.9 mg, 0.69 mmol, 2 eq) was then added in one portion and the reaction was stirred at RT. Once judged complete by TLC analysis, the resulting suspension was diluted with EtOAc and washed with brine and then dried (Na2SO4), filtered and evaporated to dryness. The resulting residue was purified by trituration or Prep-TLC to give the desired product (201 mg).
A mixture of 1-((6-fluoropyridin-3-yl)methyl)-3-(4-(2-(4-methoxyphenyl)propan-2-yl)thiazol-2-yl)urea (50 g, 0.13 mmol, 1.0 eq) and 2-aminoethanol (11.9 mg, 0.19 mmol, 1.5 eq) in EtOH was heated to 90° C. for 14 h. After the reaction was cooled down to RT, concentrated to give a residue, which was purified by column chromatography on a silica gel to afford 1-((6-((2-hydroxyethyl)amino)pyridin-3-yl)methyl)-3-(4-(2-(4-methoxyphenyl)propan-2-yl)thiazol-2-yl)urea (21 mg).
Step 1. Preparation of methyl 2-(4-methoxyphenyl)acetate
A mixture of 2-(4-methoxyphenyl)acetic acid (20.0 g, 120.4 mmol) in MeOH (100 mL) was added H2SO4 (1.2 g, 12.0 mmol, 642 μL) at 15° C. The mixture was stirred for 12 h at 85° C. The mixture was diluted with EA (400 mL), washed with sat. NaHCO3 aq (100 mL), brine (10 mL), dried over anhydrous Na2SO4, filtered and concentrated in vacuum to give a residue. The residue was purified by silica column (ethyl acetate in petroleum ether=0-15%). The desired product (21.6 g, yield: 99.7%) was obtained as yellow oil.
1H NMR (400 MHz, CDCl3) δ 7.21 (d, J=8.8 Hz, 2H) 6.87 (d, J=8.8 Hz, 2H), 3.80 (s, 3H), 3.69 (s, 3H), 3.58 (s, 2H)
Step 2. Preparation of compound methyl 2-(4-methoxyphenyl)-3-oxobutanoate
To a solution of compound obtained from step 1 above (23.8 g, 132.2 mmol) in THF (200 mL) was added LiHMDS (1 M, 159 mL) at −78° C. The mixture was stirred for 20 min at −78° C. Acetyl acetate (13.5 g, 132.2 mmol) was added to the solution. Then the mixture was warmed to 0° C. and stirred for 2 h at 0° C. The mixture was quenched with sat NH4Cl aq. (50 mL) and extracted with EA (3×50 mL). The combined organic layers were washed with brine (10 mL), dried over anhydrous Na2SO4, filtered and concentrated in vacuum. The residue was purified on silica gel chromatography (ethyl acetate in petroleum ether=0-15%) to give the desired compound (14.23 g, yield: 48.4%) as a yellow oil.
1H NMR (400 MHz, CDCl3) δ 12.97 (s, 1H), 7.25-7.23 (m, 1.5H), 7.07-7.03 (m, 2H), 6.87-6.85 (m, 2H), 4.63 (s, 0.5H), 3.80 (s, 3H), 3.78 (s, 1.5H), 3.73 (s, 1.5H), 3.67 (s, 3H), 2.15 (s, 1.5H), 1.83 (s, 3H). MS (ESI) m/z (M+H)+=223.1
Step 3. Preparation of compound methyl 2-(4-methoxyphenyl)-2-methyl-3-oxobutanoate
To a mixture of compound obtained from step 2 above (14.5 g, 65.4 mmol) and K2CO3 (45.2 g, 326.9 mmol) in ACETONE (100 mL) was added CH3I (26.0 g, 183.3 mmol) at 15° C. The mixture was stirred at 70° C. for 12 h. The mixture was filtered and the filtrate was concentrated in vacuum to give a residue. The residue was purified by silica column (ethyl acetate in petroleum ether=0-15%). The desired compound (9.76 g, yield: 63.2%) was obtained as a colorless oil.
1H NMR (400 MHz, CDCl3) δ 7.25-7.19 (m, 2H), 6.95-6.86 (m, 2H), 3.82 (s, 3H), 3.79 (s, 3H), 2.10 (s, 3H), 1.77 (s, 3H)
Step 4. Preparation of compound methyl 4-bromo-2-(4-methoxyphenyl)-2-methyl-3-oxobutanoate
To a solution of compound obtained from step 3 above (1 g, 4.2 mmol) in CHCl3 (20 mL) was added Br2 (676 mg, 4.2 mmol) at 15° C. The mixture was stirred at 73° C. for 12 h. The mixture was washed with H2O (20 mL), brine (10 mL), dried over anhydrous Na2SO4, filtered and concentrated in vacuum to give a residue. The desired product (1.03 g, crude) was obtained as a colorless oil. The crude product was directly used for the next step without further purification.
MS (ESI) m/z (M+H)+=315.1
Step 5. Preparation of compound methyl 2-(2-aminothiazol-4-yl)-2-(4-methoxyphenyl)propanoate
A mixture of compound obtained from step 4 above (1.03 g, 3.3 mmol), THIOUREA (299 mg, 3.9 mmol) and NaHCO3 (329 mg, 3.9 mmol) in MeOH (15 m L) was stirred at 50° C. for 1 h. The mixture was concentrated in vacuum directly. The residue was triturated with H2O (20 mL) at 15° C. for 10 min., filtered and the cake was concentrated in vacuum to give a residue. The desired product (0.79 g, yield: 82.68%) was obtained as a yellow solid
1H NMR (400 MHz, CDCl3) δ 7.20-7.18 (m, 2H), 6.97-6.92 (m, 2H), 6.88-6.86 (m, 2H), 5.95 (s, 1H), 3.73 (s, 3H), 3.61 (s, 3H), 1.77 (s, 3H).
Step 6. Preparation of compound methyl 2-(4-methoxyphenyl)-2-(2-((phenoxycarbonyl)amino)thiazol-4-yl)propanoate
To a mixture of compound obtained from step 5 above (300 mg, 1.03 mmoL) and PYRIDINE (97.4 mg, 1.23 mmol) in CH3CN (3 mL) was added phenyl carbonochloridate (169 mg, 1.08 mmol) at 0° C. The mixture was stirred at 15° C. for 3 h. The mixture was concentrated in vacuum directly. The residue was purified by silica column (ethyl acetate in petroleum ether=0-30%) to give the desired compound (330 mg, yield: 77.97%) which was obtained as a yellow oil.
MS (ESI) m/z (M+H)+=413.0
Step 7. Preparation of compound tert-butyl 4-(4-(1-(3-(4-(1-methoxy-2-(4-methoxyphenyl)-1-oxopropan-2-yl)thiazol-2-yl)ureido)ethyl)phenyl)piperazine-1-carboxylate
To a mixture of compound obtained from step 6 above (330 mg, 800 μmol) and tert-butyl 4-[4-(1-aminoethyl)phenyl]piperazine-1-carboxylate (269 mg, 880 μmol) in THF (2 mL) was stirred at 100° C. for 1 h under Microwave. The mixture was directly concentrated in vacuum to give a residue. The residue was purified by silica column (ethyl acetate in petroleum ether=0-80%). The desired compound (441 mg, yield: 88.37%) was obtained as a yellow oil.
MS (ESI) m/z (M+H)+=646.2
Step 8. Preparation of compound tert-butyl 4-(4-(1-(3-(4-(1-hydroxy-2-(4-methoxyphenyl)propan-2-yl)thiazol-2-yl)ureido)ethyl)phenyl)piperazine-1-carboxylate
To a solution of compound obtained from step 7 above (370 mg, 593 μmol) in THF (10 mL) was added LiBH4 (26 mg, 1.2 mmol) at 15° C. The mixture was stirred for 12 h at 15° C. The mixture was diluted with sat·NH4Cl (15 mL) and extracted with EA (3×15 mL). The organic layers were washed with brine (10 mL), dried over anhydrous Na2SO4, filtered and concentrated in vacuum. The residue was purified by silica column (ethyl acetate in petroleum ether=0-100%) to give the desired compound (307 mg, yield: 87.0%) which was obtained as a yellow solid.
1H NMR (400 MHz, CDCl3) δ 7.17 (d, J=8.4 Hz, 2H), 7.09-7.06 (m, 2H), 6.86-6.80 (m, 4H), 6.45 (s, 1H), 4.94-4.91 (m, 1H), 4.05-4.00 (m, 1H), 3.81-3.77 (m, 4 H), 3.56-3.54 (m, 4H) 3.09-3.07 (m, 4H), 1.56 (d, J=1.6 Hz, 3H), 1.49 (s, 9H), 1.46 (d, J=6.8 Hz, 3H).
Step 9. Preparation of compound 1-(4-(1-hydroxy-2-(4-methoxyphenyl)propan-2-yl)thiazol-2-yl)-3-(1-(4-(piperazin-1-yl)phenyl)ethyl)urea hydrochloride
To a solution of compound obtained from step 8 above (50 mg, 83.93 μmol) in DCM (2 mL) was added HCl/EtOAc (4 M, 2 mL) at 15° C. The mixture was stirred for 12 h at 15° C. The mixture was concentrated in vacuum to give the desired compound (34 mg, yield: 76.1%) was obtained as a yellow solid.
1H NMR (400 MHz, DMSO) δ 10.47 (br s, 1H), 9.11 (br s, 2H), 7.36-7.23 (m, 1H), 7.19 (d, J=8.8 Hz, 2H), 7.10 (d, J=8.8 Hz, 2H), 6.95 (d, J=8.8 Hz, 2H), 6.75 (d, J=8.0 Hz, 2H), 6.69 (s, 1H), 4.77-4.73 (m, 1H), 3.80-3.76 (m, 1H), 3.70 (s, 3H) 3.34-3.31 (m, 4H), 3.24-3.16 (m, 4H), 2.07 (s, 1H), 1.55 (s, 3H), 1.33 (d, J=6.8 Hz, 3H). MS (ESI) m/z (M+H)+=496.2
Step 10. Preparation of compound tert-butyl 4-(4-(1-(3-(4-(2-(4-methoxyphenyl)-1-oxopropan-2-yl)thiazol-2-yl)ureido)ethyl)phenyl)piperazine-1-carboxylate
To a solution of oxalyl dichloride (68. 2 mg, 537.14 μmo) in DCM (2 mL) was added DMSO (66 mg, 839 μmol) at −78° C. After 10 min, compound obtained from step 9 above (100 mg, 168 μmol) in DCM (2 mL) was added and stirred for 1 h at −78° C. Et3N (170 mg, 1.68 mmol) was added and stirred for 10 more min then warmed to 15° C. and stirred for another 1 h. The mixture was diluted with H2O (20 mL), extracted with DCM (3×20 mL). The organic layers were washed with brine (10 mL), dried over anhydrous Na2SO4, filtered and concentrated in vacuum to give a residue. The desired product (120 mg, crude) was obtained as a yellow oil. The crude product was directly used for the next step without further purification.
Step 11. Preparation of compound tert-butyl 4-(4-(1-(3-(4-(2-(4-methoxyphenyl)but-3-yn-2-yl)thiazol-2-yl)ureido)ethyl)phenyl)piperazine-1-carboxylate
mixture of compound obtained from step 10 above (100 mg, 168 μmol), dimethyl (1-diazo-2-oxopropyl)phosphonate (49 mg, 252.6 μmol) and K2CO3 (47 mg, 337 μmol in MeOH (5 mL) was stirred for 1 h at 15° C. The reaction was directly concentrated in vacuum. The residue was purified by prep. HPLC (column: Venusil ASB Phenyl 150*30 mm*5 um; mobile phase: [water (0.05% HCl)-ACN]; B %: 65%-95%, 10 min) to give the desired compound (50 mg, yield: 50.34%) was obtained as a yellow oil.
MS (ESI) m/z (M+H)+=590.3
Step 12. Preparation of compound 1-(4-(2-(4-methoxyphenyl)but-3-yn-2-yl)thiazol-2-yl)-3-(1-(4-(piperazin-1-yl)phenyl)ethyl)urea
The desired compound (39 mg, yield: 87.4%) was obtained as a yellow solid using De-BOC method.
1H NMR (400 MHz, DMSO-d6) δ 10.50 (br s, 1H), 9.22 (br s, 2H), 7.31 (d, J=8.8 Hz, 2H), 7.19 (d, J=8.4 Hz, 3H), 6.95 (d, J=8.4 Hz, 2H), 6.85 (dd, J=8.4, 1.2 Hz, 2H), 6.81-6.79 (m, 1H), 4.76-4.73 (m, 1H), 3.71 (s, 3H), 3.39 (s, 1H), 3.35-3.32 (m, 4H) 3.24-3.16 (m, 4H), 1.82 (d, J=2.4 Hz, 3H), 1.33 (d, J=6.8 Hz, 3H).
MS (ESI) m/z (M+Na)*=512.3
Step 1: Preparation of tert-butyl 4-(4-((3-(4-(2-(4-cyclopropylphenyl)propan-2-yl)thiazol-2-yl)ureido)methyl)phenyl)piperazine-1-carboxylate
To a solution of compound obtained from step 1 above (81 mg, 0.13 mmol) in 1,4-dioxane (4 mL) and H2O (1 mL) was added cyclopropylboronic acid (14 mg, 0.16 mmol), Pd(dppf)Cl2 (10 mg, 0.013 mmol), KOAc (25 mg, 0.26 mmol). The reaction mixture was stirred at 15° C. overnight under N2 atmosphere. The reaction progress was monitored by TLC. After the completion of the reaction, the mixture was filtered through a pad of celite, washed with EA. The filtrate was removed under reduced pressure and the residue was purified by column chromatography on silica gel (PE/EA=2:1) to give the desired compound (45 mg, yield: 60.2%) as a white solid.
Step 2. Preparation of compound 1-(4-(2-(4-cyclopropylphenyl)propan-2-yl)thiazol-2-yl)-3-(4-(piperazin-1-yl)benzyl)urea
The desired compound was obtained as a white solid (40 mg, HCl salt, yield: 100%) with the procedure described in example 9. MS (ESI) m/z (M+H)+=476.2.
Step 1. Preparation of compound tert-butyl N-(2,2-dideuterio-2-hydroxy-ethyl)carbamate
To a solution of methyl 2-((tert-butoxycarbonyl)amino)acetate (1 g, 5.29 mmol) in THF (20 mL) was added LiAlD4 (364.8 mg, 7.93 mmol) at 0° C. and then the mixture was stirred at 80° C. for 3 h. EA (20 mL) was added dropwise and the H2O (5 mL), and then extracted with EA (100 mL×3). The combined organic phase was washed with brine (20 mL×3), dried over anhydrous Na2SO4, filtered and concentrated to give a residue. The desired compound (610 mg, yield: 70.7%) was obtained as yellow oil, which was used into the next step without further purification.
1H NMR (400 MHz, CDCl3) δ 5.17 (br s, 1H), 3.24 (d, J=5.6 Hz, 2H), 3.08 (br s, 1H), 1.42 (s, 9H).
Step 2. Preparation of compound 2-amino-1,1-dideuterio-ethanol
A mixture of compound obtained from step 1 above (610 mg, 3.74 mmol) in HCl/MeOH (4 M, 5 mL) was stirred at 25° C. for 3 h. The reaction mixture was concentrated. The desired compound (520 mg, crude, HCl) was obtained as yellow oil, which was used into the next step without further purification.
1H NMR (400 MHz, DMSO-d6) δ 2.80 (q, J=5.7 Hz, 2H).
Step 3. Preparation of compound phenyl N-[4-[1-(4-chlorophenyl)-1-methyl-prop-2-ynyl]thiazol-2-yl]carbamate
To a solution of 4-[1-(4-chlorophenyl)-1-methyl-prop-2-ynyl]thiazol-2-amine (500 mg, 1.90 mmol) and pyridine (752.60 mg, 9.51 mmol) in McCN (20 mL) was added phenyl carbonochloridate (327.7 mg, 2.09 mmol) at 0° C. and then the mixture was stirred at 0° C. for 1 h. The residue was poured into water (30 mL). The aqueous phase was extracted with ethyl acetate (80 mL×3). The combined organic phase was washed with brine (10 mL×2), dried with anhydrous Na2SO4, filtered and concentrated in vacuum. The desired compound (830 mg, crude) was obtained as yellow oil, which was used into the next step without further purification.
MS (ESI) m/z (M+H)+=383.0
Step 4. Preparation of compound 1-[4-[1-(4-chlorophenyl)-1-methyl-prop-2-ynyl]thiazol-2-yl]-3-(2,2-dideuterio-2-hydroxy-ethyl)urea
A mixture of compound obtained from step 3 above (400 mg, 1.04 mmol), compound obtained from step 2 above (98.9 mg, 1.57 mmol) and DMAP (12.8 mg, 104.48 umol) in DCE (20 mL) was stirred at 80° C. for 5 h. The reaction mixture was concentrated. The residue was purified by prep-HPLC (column: Xtimate C18 150*40 mm*5 um; mobile phase: [water (HCl)-ACN]; B %: 28%-58%, 10 min). The desired compound (90 mg, yield: 24.5%) was obtained as a white solid.
MS (ESI) m/z (M+H)+=352.1.
SFC: Column: ChiralPak IG-3 100×4.6 mm I.D., 3 um Mobile phase: A: CO2 B:Ethanol (0.05% DEA) Gradient: from 5% to 40% of B in 5.5 min and hold 40% for 3 min, then 5% of B for 1.5 min Flow rate: 2.5 mL/min Column temperature:40 C, (P1: Rf=4.159 min, P2: Rf=4.831 min).
Step 5. Preparation of compound 1-[4-[1-(4-chlorophenyl)-1-methyl-prop-2-ynyl]thiazol-2-yl]-3-(2,2-dideuterio-2-hydroxy-ethyl)urea
The compound obtained from step 4 above ((90 mg, 255.79 umol) was separated by SFC (column: DAICEL CIHIRALPAK IG (250 mm*30 mm, 10 um); mobile phase: [0.1% NH3H2O ETOH]; B %: 40%-40%, min). Chiral isomers 1 (26.85 mg, yield: 29.8%) was obtained as a white solid.
1H NMR (400 MHz, CDCl3) δ 7.34-7.28 (m, 2H), 7.22-7.19 (m, 2H), 6.69 (s, 1H), 3.23 (d, J=5.5 Hz, 2H), 2.48 (s, 1H), 1.84 (s, 3H). MS (ESI) m/z (M+H)+=351.9. SFC Rf=4.151 min.
Chiral isomers 2 (27.90 mg, yield: 31.0%) was obtained as a white solid.
1H NMR (400 MHz, CDCl3) δ 7.43-7.35 (m, 2H), 7.31-7.27 (m, 2H), 6.76 (s, 1H), 3.31 (d, J=5.5 Hz, 2H), 2.55 (s, 1H), 1.92 (s, 3H). MS (ESI) m/z (M+H)+=351.9. SFC: Rf=4.815 min.
Carboxylic acids (1 equiv), EDCI (2-2.5 equiv), with or without HOBt (2 equiv) and DIEA (3 equiv)/pyridine/DMAP were dissolved in THF/DMF and stirred for 15-30 min at RT. Amine (1 equiv) was then added in one portion and the reaction was stirred at RT to 70° C. for 2-16 hours. Once the reaction was completed, the resulting suspension was diluted with organic solvent and washed with brine and then dried. After filtration and evaporation, the resulting residue was purified by trituration/Prep-TLC/chromatography/Prep-HPLC to give the product.
To a solution of 4-((2-hydroxyethyl)amino)benzoic acid (200 mg, 1.10 mmol) and 4-[1-(4-methoxyphenyl)-1-methyl-ethyl]thiazol-2-amine (261.98 mg, 919.85 umol, HCl) in Py (8 mL) was added EDCI (440.84 mg, 2.30 mmol). The mixture was stirred at 70° C. for 16 hr. The reaction mixture was concentrated to give a residue. The residue was purified by prep-HPLC (column: Agela ASB 150×25 mm×5 um; mobile phase: [water (0.05% HCl)-ACN]; B %: 48%-78%, 10 min). The desired compound (52 mg, yield: 13.57%) was obtained as a pale yellow solid.
1H NMR (400 MHz, DMSO-d6) δ 12.06 (br s, 1H), 7.87 (d, J=8.8 Hz, 2H), 7.12 (d, J=8.8 Hz, 2H), 6.86 (s, 1H), 6.82 (d, J=8.8 Hz, 2H), 6.62 (d, J=8.8 Hz, 2H), 3.70 (s, 3H), 3.54 (t, J=5.9 Hz, 2H), 3.16 (t, J=5.9 Hz, 2H), 1.62 (s, 6H). MS (ESI) m/z (M+H)+=412.5.
The acid chloride was obtained by using SOCl2 in appropriate solvent like DCM. To the acis chloride solution TEA or pyridine (3 equiv) a and mine (1 equiv) in DCM were added slowly at 0° C. under N2, and further stirred for 0.5-2 h at RT. Once the reaction was completed, it was quenched with H2O, extracted by EA and washed with brine then dried (Na2SO4), filtered and evaporated to dryness. The resulting residue was purified by trituration/Prep-TLC/chromatography/Prep-HPLC to give the product.
To a solution of 4-(4-tert-butoxycarbonylpiperazin-1-yl)-2,6-difluoro-benzoic acid (150 mg, 438.16 umol) in DCM (6 mL) was added SOCl2 (31.8 uL, 438.16 umol). The mixture was stirred at 25° C. for 1 hr. The Py (176.74 uL, 2.19 mmol) was added and the reaction was stirred at 25° C. for 5 min, then 4-[1-(4-chlorophenyl)-1-methyl-prop-2-ynyl]thiazol-2-amine (115.07 mg, 437.94 umol) was added and the mixture was stirred at 25° C. for 16 hr. The reaction mixture was concentrated to give a residue. The residue was purified by flash silica gel chromatography (PE:EA=1:0 to 1:1). The desired compound (152 mg, yield: 54.4%) was obtained as a colorless oil.
MS (ESI) m/z (M+H)+=587.1.
Step 1. Preparation of compound methyl 2-(4-chlorophenyl)-2-(imidazo[1,2-a]pyrimidin-2-yl)propanoate
A mixture of pyrimidin-2-amine (1.0 g, 10.5 mmol) and methyl 4-bromo-2-(4-chlorophenyl)-2-methyl-3-oxo-butanoate (3.36 g, 10.5 mmol) in EtOH (20 mL) was stirred at 80° C. for 16 h. The reaction was concentrated under reduced pressure and diluted with CH2Cl2 (40 mL) and sat. aq NaHCO3 (20 mL), and the water phase was extracted with CH2Cl2 (3×30 mL). The combined organic layers were washed with sat. aq NaHCO3 (2×20 mL), dried over Na2SO4, filtered and concentrated under reduced pressure. The residue was purified by column chromatography (SiO2, Petroleum ether/Ethyl acetate=I/O to 0/1) to afford methyl 2-(4-chlorophenyl)-2-imidazo[1,2-a]pyrimidin-2-yl-propanoate (1.48 g, yield: 40.1%) as a white solid.
MS (ESI) m/z (M+H)+=316.0.
Step 2. Preparation of compound methyl 2-(2-amino-1H-imidazol-4-yl)-2-(4-chlorophenyl)propanoate
To a solution of methyl 2-(4-chlorophenyl)-2-imidazo[1,2-a]pyrimidin-2-yl-propanoate (600 mg, 1.90 mmol) in dioxane (5 mL) was added NH2NH2·H2O (650 mg, 11.04 mmol, 85% purity). After addition, the reaction mixture was stirred at 80° C. for 16 h. The reaction mixture was concentrated in vacuum. The residue was purified by column chromatography (SiO2, DCM:MeOH=100/1-10/1) to afford methyl 2-(2-amino-1H-imidazol-4-yl)-2-(4-chlorophenyl)propanoate (60 mg, yield: 33.9%) as white solid.
MS (ESI) m/z (M+H)+=280.1.
1H NMR (400 MHz, CD3OD) δ 7.29 (d, J=8.4 Hz, 2H), 7.20 (d, J=8.4 Hz, 2H), 6.32 (s, 1H), 3.72 (s, 3H), 1.79 (s, 3H).
Step 3. Preparation of compound tert-butyl 4-(4-((4-(2-(4-chlorophenyl)-1-methoxy-1-oxopropan-2-yl)-1H-imidazol-2-yl)carbamoyl)-3,5-difluorophenyl)piperazine-1-carboxylate
SOCl2 (92 mg, 772 umol) was added to a solution of 4-(4-tert-butoxycarbonylpiperazin-1-yl)-2,6-difluoro-benzoic acid (220 mg, 644 umol) in DCM (10 mL), then DMF (13 mg, 172 umol) was added and the reaction mixture was stirred at 25° C. for 1 h, followed by Py (204 mg, 2.57 mmol) was added into the reaction mixture and stirred at 25° C. for 10 min, then methyl 2-(2-amino-1H-imidazol-4-yl)-2-(4-chlorophenyl)propanoate (120 mg, 429 umol) was added into the reaction mixture and stirred at 25° C. for 16 h. The reaction mixture was washed with sat. NaHCO3 (5 mL), brine (5 mL), dried over Na2SO4, filtered and concentrated in vacuum. The residue was purified by column chromatography (SiO2, Petroleum ether/Ethyl acetate=10/1 to 2/1) to afford tert-butyl 4-[4-[[4-[1-(4-chlorophenyl)-2-methoxy-1-methyl-2-oxo-ethyl]-1H-imidazol-2-yl]carbamoyl]-3,5-difluoro-phenyl]piperazine-1-carboxylate (120 mg, yield: 38.9% yield, 84% purity) as colorless gum.
MS (ESI) m/z (M+H)+=604.1.
Step 4. Preparation of compound tert-butyl 4-(4-((4-(2-(4-chlorophenyl)-1-hydroxypropan-2-yl)-1H-imidazol-2-yl)carbamoyl)-3,5-difluorophenyl)piperazine-1-carboxylate
To a solution of tert-butyl 4-[4-[[4-[1-(4-chlorophenyl)-2-methoxy-1-methyl-2-oxo-ethyl]-1H-imidazol-2-yl]carbamoyl]-3,5-difluoro-phenyl]piperazine-1-carboxylate (120 mg, 199 umol) in THF (8 mL) was added LiBH4 (4 M, 248 uL) at 0° C. After addition, the reaction mixture was stirred at 25° C. for 16 h. The reaction mixture was poured into 5 mL of sat. NH4Cl and extracted with EtOAc (8 mL×2), the extracts was washed with water (8 mL×3), brine (8 mL), dried over Na2SO4, filtered and concentrated in vacuum to afford tert-butyl 4-[4-[[4-[1-(4-chlorophenyl)-2-hydroxy-1-methyl-ethyl]-1H-imidazol-2-yl]carbamoyl]-3,5-difluoro-phenyl]piperazine-1-carboxylate (110 mg, crude) as light brown gum which was used in next step without any purification.
MS (ESI) m/z (M+H)+=576.1.
Step 5. Preparation of compound tert-butyl 4-(4-((4-(2-(4-chlorophenyl)-1-oxopropan-2-yl)-1H-imidazol-2-yl)carbamoyl)-3,5-difluorophenyl)piperazine-1-carboxylate
To a solution of tert-butyl 4-[4-[[4-[1-(4-chlorophenyl)-2-hydroxy-1-methyl-ethyl]-1H-imidazol-2-yl]carbamoyl]-3,5-difluoro-phenyl]piperazine-1-carboxylate (170 mg, 295 umol) in DCM (10 mL) was added DMP (500 mg, 1.18 mmol), after addition, the reaction mixture was stirred at 25° C. for 4 h. The reaction mixture was diluted with DCM (10 mL), washed with sat. NaHCO3/sat. Na2S2O3 (10 mL/10 mL) for 3 times, then washed with brine (10 mL), dried over Na2SO4, filtered and concentrated in vacuum to afford tert-butyl 4-[4-[[4-[1-(4-chlorophenyl)-1-methyl-2-oxo-ethyl]-1H-imidazol-2-yl]carbamoyl]-3,5-difluoro-phenyl]piperazine-1-carboxylate (150 mg, crude) as light brown gum which was used in next step without any purification.
Step 6. Preparation of compound tert-butyl 4-(4-((4-(2-(4-chlorophenyl)but-3-yn-2-yl)-1H-imidazol-2-yl)carbamoyl)-3,5-difluorophenyl)piperazine-1-carboxylate
To a solution of tert-butyl 4-[4-[[4-[1-(4-chlorophenyl)-1-methyl-2-oxo-ethyl]-1H-imidazol-2-yl]carbamoyl]-3,5-difluoro-phenyl]piperazine-1-carboxylate (150 mg, 261 umol) and 1-diazo-1-dimethoxyphosphoryl-propan-2-one (75.3 mg, 392 umol) in MeOH (8 mL) was added K2CO3 (72.2 mg, 522.63 umol). After addition, the reaction mixture was stirred 25° C. for 16 h. The reaction mixture was concentrated in vacuum and the residue was diluted with 10 mL of water and extracted with EtOAc (10 mL×2), the combined extracts was washed with brine (10 mL), dried over Na2SO4, filtered and concentrated in vacuum. The residue was purified by prep-HPLC (FA condition) to afford tert-butyl 4-[4-[[4-[1-(4-chlorophenyl)-1-methyl-prop-2-ynyl]-1H-imidazol-2-yl]carbamoyl]-3,5-difluoro-phenyl]piperazine-1-carboxylate (12 mg, yield: 8.1%) as off-white solid.
Step 7. Preparation of compound N-(4-(2-(4-chlorophenyl)but-3-yn-2-yl)-1H-imidazol-2-yl)-2,6-difluoro-4-(piperazin-1-yl)benzamide
To a solution of tert-butyl 4-[4-[[4-[I-(4-chlorophenyl)-1-methyl-prop-2-ynyl]-1H-imidazol-2-yl]carbamoyl]-3,5-difluoro-phenyl]piperazine-1-carboxylate (12 mg, 21.05 umol) in MeOH (0.3 mL) was added HCl/dioxane (4 M, 900 uL). After addition, the reaction mixture was stirred at 25° C. for 1 h. The reaction mixture was concentrated in vacuum. The residue was purified by prep-HPLC (TFA condition) to afford N-[4-[1-(4-chlorophenyl)-1-methyl-prop-2-ynyl]-1H-imidazol-2-yl]-2,6-difluoro-4-piperazin-1-yl-benzamide (5 mg, yield: 40.2% yield, 2HCl salt) as light brown solid.
MS (ESI) m/z (M+Na)*=492.3.
1H NMR (400 MHz, CD3OD) δ 7.52 (br d, J=8.4 Hz, 2H), 7.40 (br d, J=8.4 Hz, 2H), 7.22 (s, 1H), 6.76 (br d, J=12.4 Hz, 2H), 3.65-3.59 (m, 4H), 3.39-3.32 (m, 4H), 3.20 (s, 1H), 1.97 (s, 3H).
Step 1. Preparation of compound methyl 2-(2-aminooxazole-4-yl)-2-(4-chlorophenyl)propanoate
To a solution of methyl 4-bromo-2-(4-chlorophenyl)-2-methyl-3-oxobutanoate (1.00 g, 3.13 mmol) in EtOH (30 mL) was added urea (282 mg, 4.69 mmol) and the mixture was stirred at 80° C. for 20 h. The reaction mixture was concentrated under reduced pressure. The residue was purified by column chromatography (SiO2, Petroleum ether/Ethyl acetate=1/0 to 3/1) to afford methyl 2-(2-aminooxazole-4-yl)-2-(4-chlorophenyl)propanoate (50.0 mg, yield: 4.2%) as a yellow solid.
MS (ESI) m/z (M+H)+=281.1.
1H NMR (400 MHz, CD3OD) δ 7.31 (s, 4H), 6.98 (s, 1H), 3.71 (s, 3H), 1.85-1.79 (m, 3H).
Step 2. Preparation of compound tert-butyl 4-(4-((4-(2-(4-chlorophenyl)-1-methoxy-1-oxopropan-2-yl)oxazol-2-yl)carbamoyl)-3,5-difluorophenyl)piperazine-1-carboxylate
SOCl2 (38.0 mg, 321 umol) was added to a solution of 4-(4-tert-butoxycarbonylpiperazin-1-yl)-2,6-difluoro-benzoic acid (91.0 mg, 267 umol) in DCM (5 mL). DMF (5.0 mg, 71.3 umol) was added and the reaction mixture was stirred at 25° C. for 1 h. Then Py (85.0 mg, 1.07 mmol) was added to the above reaction mixture and stirred at 25° C. for 10 min, then methyl 2-(2-aminooxazole-4-yl)-2-(4-chlorophenyl)propanoate (50.0 mg, 178 umol) was added into the reaction mixture and stirred at 25° C. for 16 h. The reaction mixture was washed with sat·NaHCO3 (3 mL), brine (3 mL), dried over Na2SO4, filtered and concentrated in vacuum. The residue was purified by column chromatography (SiO2, Petroleum ether/Ethyl acetate=10/1 to 2/1) to afford tert-butyl 4-[4-[[4-[1-(4-chlorophenyl)-2-methoxy-1-methyl-2-oxo-ethyl]oxazol-2-yl]carbamoyl]-3,5-difluoro-phenyl]piperazine-1-carboxylate (42.0 mg, yield: 30%) as colorless gum.
MS (ESI) m/z (M+H)+=605.1.
Step 3. Preparation of compound tert-butyl 4-(4-((4-(2-(4-chlorophenyl)-1-hydroxypropan-2-yl)oxazol-2-yl)carbamoyl)-3,5-difluorophenyl)piperazine-1-carboxylate
To a solution of LiBH4 (4 M, 83 uL) in THF (3 mL) was added a solution of tert-butyl 4-[4-[[4-[1-(4-chlorophenyl)-2-methoxy-1-methyl-2-oxo-ethyl]oxazol-2-yl]carbamoyl]-3,5-difluoro-phenyl]piperazine-1-carboxylate (40.0 mg) in THF (2 mL) at 0° C. under N2 atmosphere. After addition, the reaction mixture was stirred at 25° C. for 2 h. The reaction mixture was poured into 5 mL of sat. NH4Cl and extracted with EtOAc (8 mL×2), the extracts was washed with water (8 mL×3), brine (8 mL), dried over Na2SO4, filtered and concentrated in vacuum to afford tert-butyl 4-[4-[[4-[1-(4-chlorophenyl)-2-hydroxy-1-methyl-ethyl]oxazol-2-yl]carbamoyl]-3,5-difluoro-phenyl]piperazine-1-carboxylate (28.0 mg, crude) as white solid which was used in next step without any purification.
Step 4. Preparation of compound tert-butyl 4-(4-((4-(2-(4-chlorophenyl)-1-oxopropan-2-yl)oxazol-2-yl)carbamoyl)-3,5-difluorophenyl)piperazine-1-carboxylate
To a solution of tert-butyl 4-[4-[[4-[1-(4-chlorophenyl)-2-hydroxy-1-methyl-ethyl]oxazol-2-yl]carbamoyl]-3,5-difluoro-phenyl]piperazine-1-carboxylate (28.0 mg, crude) in DCM (5 mL) was added DMP (41.0 mg, 97.05 umol), after addition, the reaction mixture was stirred at 25° C. for 3 h. The reaction mixture was diluted with DCM (10 mL), washed with sat·NaHCO3/Na2S2O3 (10 mL/10 mL) for 3 times, then brine (10 mL), dried over Na2SO4, filtered and concentrated in vacuum to afford tert-butyl 4-[4-[[4-[1-(4-chlorophenyl)-1-methyl-2-oxo-ethyl]oxazol-2-yl]carbamoyl]-3,5-difluoro-phenyl]piperazine-1-carboxylate (30.0 mg, crude) as light brown solid which was used in next step without any purification.
MS (ESI) m/z (M+H)+=575.1.
Step 5. Preparation of compound tert-butyl 4-(4-((4-(2-(4-chlorophenyl)but-3-yn-2-yl)oxazol-2-yl)carbamoyl)-3,5-difluorophenyl)piperazine-1-carboxylate
To a solution of tert-butyl 4-[4-[[4-[1-(4-chlorophenyl)-1-methyl-2-oxo-ethyl]oxazol-2-yl]carbamoyl]-3,5-difluoro-phenyl]piperazine-1-carboxylate (30.0 mg, crude) and 1-diazo-1-dimethoxyphosphoryl-propan-2-one (15.0 mg, 78.3 umol) in MeOH (4 mL) was added K2CO3 (14.0 mg, 104 umol). After addition, the reaction mixture was stirred 25° C. for 16 h. The reaction mixture was concentrated in vacuum, the residue was diluted with H2O (5 mL), extracted with EtOAc (5 mL×3), the combined extracts was washed with brine (5 mL), dried over Na2SO4, filtered and concentrated in vacuum to afford tert-butyl 4-[4-[[4-[1-(4-chlorophenyl)-1-methyl-prop-2-ynyl]oxazol-2-yl]carbamoyl]-3,5-difluoro-phenyl]piperazine-1-carboxylate (28.0 mg, crude) as light brown gum.
MS (ESI) m/z (M+H)+=571.1.
Step 6. Preparation of compound N-(4-(2-(4-chlorophenyl)but-3-yn-2-yl)oxazol-2-yl)-2,6-difluoro-4-(piperazin-1-yl)benzamide
To a solution of tert-butyl 4-[4-[[4-[1-(4-chlorophenyl)-1-methyl-prop-2-ynyl]oxazol-2-yl]carbamoyl]-3,5-difluoro-phenyl]piperazine-1-carboxylate (25.0 mg, crude) in DCM (2 mL) was added TFA (2 mL). After addition, the reaction mixture was stirred at 25° C. for 1 h. The reaction mixture was concentrated in vacuum. The residue was purified by prep-HPLC (FA condition) to afford N-[4-[1-(4-chlorophenyl)-1-methyl-prop-2-ynyl]oxazol-2-yl]-2,6-difluoro-4-piperazin-1-yl-benzamide (7.5 mg, yield: 28.7%, TFA salt) as light brown solid.
MS (ESI) m/z (M+H)+=471.3.
1H NMR (400 MHz, CD3OD) 67.64 (s, 1H), 7.58 (br d, J=8.0 Hz, 2H), 7.39-7.29 (m, 2H), 6.72 (br d, J=11.8 Hz, 2H), 3.65-3.54 (m, 4H), 3.42-3.35 (m, 4H), 2.98 (s, 1H), 1.90 (s, 3H).
Carboxylic acids (1 equiv), HATU (1.2 equiv) or HBTU or PyBOP, and TEA or DIEA (3 equiv.) were dissolved in appropriate organic solvent, like THF or DMF and stirred for 15-30 min at RT. Amine (1-1.5 equiv.) was then added in one portion and the reaction was stirred at RT−100° C. for 4-16 hours. Once the reaction was completed, the resulting suspension was diluted with organic solvent and washed with brine and then dried. After filtration and evaporation, the resulting residue was purified by trituration/Prep-TLC/chromatography/Prep-HPLC to give the product.
To a solution of 3-[tert-butyl(diphenyl)silyl]oxycyclobutanecarboxylic acid (1.36 g, 3.84 mmol), in DCM (10 mL) was added PyBOP (2.00 g, 3.84 mmol) at 25° C., After stirred for 10 min, methyl 2-(2-aminothiazol-4-yl)-2-(4-bromophenyl)propanoate (523.61 mg, 1.53 mmol) and DIPEA (594.97 mg, 4.60 mmol) was added at 25° C. and the mixture was stirred for 12 h at 25° C. The mixture was diluted with DCM (30 mL), washed with H2O (10 mL), brine (10 mL), dired over anhydrous Na2SO4, filtered and concentrated in vacuum. The obtained residue was purified by silica column (ethyl acetate in petroleum ether=0-25%). The desired compound (1.4 g, crude) was obtained as yellow oil. MS (ESI) m/z (M+H)+=643.1
1H NMR (400 MHz, CD3OD) δ 8.75-8.74 (m, 1 H), 8.43-8.40 (m, 1 H), 7.44-7.42 (m, 2 H), 7.33- 7.31 (m, 1 H), 7.22-7.20 (m, 2 H), 6.98 (s, 1 H), 4.08-4.06 (m, 4 H), 3.44- 3.42 (m, 4 H), 1.72 (s, 6 H).
1H NMR (400 MHz, CDCl3) δ 8.42 (s, 1H), 8.25 (s, 1H), 7.75 (dd, J = 8.6, 1.8 Hz, 1H), 7.44 (d, J = 8.6 Hz, 1H), 7.41-7.36 (m, 2H), 7.31-7.27 (m, 1H), 7.15-7.11 (m, 2H), 6.68 (s, 1H), 6.65 (s, 1H), 1.67 (d, J = 6.9 Hz, 6H).
1H NMR (400 MHz, DMSO-d6) δ 12.29 (br s, 1 H), 9.42 (br s, 2 H), 8.02- 8.00 (m, 2 H), 7.13-7.11 (m, 1 H), 7.05-7.03 (m, 2 H), 6.90 (s, 1 H), 6.83- 6.80 (m, 2 H), 3.69 (s, 3 H), 3.58-3.56 (m, 4 H), 3.17-3.16 (m, 4 H), 1.63 (s, 6 H).
1H NMR (400 MHz, DMSO-d6) δ 12.51 (br s, 1H), 9.28 (br s, 2H), 9.00 (s, 2H), 7.49-7.41 (m, 2H), 7.19-7.12 (m, 2H), 7.04 (s, 1H), 4.13-3.99 (m, 4H), 3.21-3.15 (m, 4H), 1.64 (s, 6H).
1H NMR (400 MHz, CD3OD) δ 7.54-7.46 (m, 2H), 7.21 (d, J = 8.8 Hz, 2H), 7.12 (s, 1H), 6.97 (d, J = 9.8 Hz, 2H), 4.39 (s, 2H), 3.43-3.37 (m, 4H), 3.36-3.32 (m, 4H), 1.71 (s, 6H).
1H NMR (400 MHz, CD3OD) δ 7.86 (br d, J = 8.56 Hz, 1 H), 7.78 (dd, J = 13.57, 1.83 Hz, 1 H), 7.25-7.17 (m, 3 H), 7.07 (s, 1 H), 6.87 (d, J = 8.80 Hz, 2 H), 3.76 (s, 3 H), 3.49 (br d, J = 5.14 Hz, 4 H), 3.41 (br d, J = 5.14 Hz, 4 H), 1.73 (s, 6 H).
1H NMR (400 MHz, DMSO-d6) δ 7.65 (s, 2H), 7.12 (br d, J = 8.8 Hz, 2H), 6.93-6.87 (m, 2H), 6.82 (d, J = 8.8 Hz, 2H), 3.85 (s, 3H), 3.70 (s, 3H), 2.98 (br s, 4H), 2.82 (br s, 4H), 1.63 (s, 6H).
1H NMR (400 MHz, DMSO-d6) δ 12.67 (br s, 1H), 9.61 (br s, 1H), 8.59 (br d, J = 7.9 Hz, 1H), 8,13 (d, J = 8.2 Hz, 2H), 7.78 (br d, J = 8.2 Hz, 2H), 7.13 (d, J = 8.6 Hz, 2H), 6.98 (s, 1H), 6.82 (d, J = 8.6 Hz, 2H), 4.59-4.34 (m, 2H), 3.95 (br s, 8H), 3.70 (s, 3H), 3.49-3.43 (m, 2H), 1.64 (s, 6H)
1H NMR (400 MHz, DMSO-d6) δ 11.79 (br s, 1H), 8.26 (br s, 3H), 8.01 (d, J = 9.0 Hz, 2H), 7.20- 7.13 (m, 2H), 6.85-6.80 (m, 2H), 6.79 (s, 1H), 6.62 (d, J = 8.8 Hz, 2H), 4.05- 3.90 (m, 1H), 3.73 (s, 3H), 3.62-3.54 (m, 2H), 3.48- 3.38 (m, 2H), 2.42-2.35 (m, 1H), 2.20-2.13 (m, 1H), 1.66 (s, 6H).
1H NMR (400 MHz, CD3OD) δ 8.78 (d, J = 1.71 Hz, 1 H), 8.43 (br d, J = 7.82 Hz, 1 H), 7.34 (br d, J = 9.29 Hz, 1 H), 7.22 (d, J = 8.80 Hz, 2 H), 7.06 (s, 1 H), 6.87 (d, J = 8.80 Hz, 2 H), 4.09 (br s, 4 H), 3.76 (s, 3 H), 3.43 (br s, 4 H), 1.73 (s, 6 H).
1H NMR (400 MHz, DMSO-d6) δ 12.66 (br s, 1H), 8.75 (s, 1H), 8.63 (br s, 3H), 8.40 (d, J = 10.3 Hz, 1H), 7.16-7.06 (m, 3H), 6.96 (s, 1H), 6.82 (d, J = 8.8 Hz, 2H), 4.08-3.98 (m, 1H), 3.92-3.80 (m, 3H), 3.70 (s, 4H), 2.41- 2.19 (m, 2H), 1.63 (s, 6H)
1H NMR (400 MHz, DMSO-d6) δ 11.64 (br s, 1H), 9.39 (br s, 2H), 8.44- 8.37 (m, 1H), 8.03 (d, J = 8.8 Hz, 1H), 7.56 (d, J = 8.6 Hz, 1H), 7.16 (d, ) = 8.8 Hz, 2H), 6.94 (s, 1H), 6.83 (d, J = 8.8 Hz, 2H), 3.70 (s, 3H), 3.69-3.63 (m, 4H), 3.28-3.16 (m, 4H), 1.63 (s, 6H).
1H NMR (400 MHz, DMSO-d6) δ 12.37 (br s, 1 H), 9.28 (br s, 2 H), 8.83 (d, J = 1.54 Hz, 1 H), 8.23 (br d, J = 9.26 Hz, 1 H), 7.11- 7.04 (m, 4 H), 6.99 (d, J = 9.04 Hz, 1 H), 6.94 (s, 1 H), 3.89 (br s, 4 H), 3.16 (br s, 4 H), 2.23 (s, 3 H), 1.63 (s, 6 H).
1H NMR (400 MHz, CD3OD) δ 8.12 (d, J = 8.07 Hz, 2 H), 7.83 (d, J = 8.31 Hz, 2 H), 7.20-7.16 (m, 2 H), 7.14-7.10 (m, 2 H), 7.08 (s, 1 H), 4.57 (s, 2 H), 3.64 (br s, 8 H), 3.01 (s, 3 H), 2.29 (s, 3 H), 1.73 (s, 6 H).
1H NMR (400 MHz, CD3OD) δ 8.08-7.96 (m, 2 H), 7.48 (br d, J = 6.61 Hz, 2 H), 7.26-7.16 (m, 2 H), 7.13-7.03 (m, 1 H), 6.86 (br d, J = 6.84 Hz, 2 H), 3.75 (s, 3 H), 3.56-3.45 (m, 2 H), 3.23-3.09 (m, 2 H), 3.03 (br t, J = 12.13 Hz, 1 H), 2.15-2.03 (m, 2 H), 1.94 (q, J = 13.38 Hz, 2 H), 1.72 (s, 6 H).
1H NMR (400 MHz, DMSO-d6) δ 12.18 (br s, 1H), 9.99 (br s, 1H), 8.39 (br s, 1H), 8.04 (d, J = 8.8 Hz, 2H), 7.15-7.07 (m, 2H), 6.87 (s, 1H), 6.80 (dd, J = 1.9, 8.9 Hz, 4H), 4.46 (br s, 2H), 3.89-3.72 (m, 4H), 3.68 (s, 3H), 2.95- 2.82 (m, 1H), 1.83 (br dd, J = 5.8, 10.0 Hz, 1H), 1.61 (s, 6H)
1H NMR (400 MHz, CDCl3) δ 8.28 (br s, 1 H) 8.13-8.18 (m, 1 H) 7.21 (d, J = 8.80 Hz, 2 H) 6.90 (d, J = 8.80 Hz, 2 H) 6.66 (s, 1 H) 3.82 (s, 3 H) 1.74 (s, 6 H)
1H NMR (400 MHz, CD3OD) δ 9.05 (d, J = 1.76 Hz, 1 H), 9.08-9.00 (m, 1 H), 8.33 (dd, J = 8.16, 2.43 Hz, 1 H), 7.65 (d, J = 8.16 Hz, 1 H), 7.39 (d, J = 8.82 Hz, 2 H), 7.19 (d, J = 8.60 Hz, 2 H), 6.88 (s, 1 H), 3.73 (s, 2 H), 3.67 (t, J = 6.06 Hz, 2 H), 2.49- 2.67 (m, 10 H), 1.69 (s, 6 H).
1H NMR (400 MHz, CDCl3) δ 11.35 (br s, 1H), 8.69-8.56 (m, 1H), 8.16 (d, J = 8.1 Hz, 1H), 7.72- 7.62 (m, 1H), 7.30-7.25 (m, 2H), 7.23-7.18 (m, 2H), 6.88 (d, J = 8.8 Hz, 2H), 6.61 (s, 1H), 3.79 (s, 3H), 1.80 (s, 6H).
1H NMR (400 MHz, CD3OD) δ 8.71 (d, J = 2.45 Hz, 1 H), 8.04 (dd, J = 9.17, 2.57 Hz, 1 H), 7.17 (d, J = 8.80 Hz, 2 H), 6.85- 6.78 (m, 3 H), 6.74 (s, 1 H), 3.74 (s, 3 H), 3.73- 3.69 (m, 6 H), 2.63-2.59 (m, 4 H), 2.57 (t, J = 5.87 Hz, 2 H), 1.67 (s, 6 H).
1H NMR (400 MHz, DMSO-d6) δ 12.31-12.23 (m, 1H), 8.79 (br s, 1H), 8.21-8.05 (m, 2H), 7.45 (br d, J = 8.4 Hz, 2H), 7.16 (br d, J = 7.9 Hz, 2H), 6,98 (br s, 1H), 6.89-6.83 (m, 1H), 4.54-4.38 (m, 2H), 3.62 (br s, 5H), 3.57-3.47 (m, 3H), 2.44-2.39 (m, 2H), 1.63 (br s, 6H)
1H NMR (400 MHz, DMSO-d6) δ 12.66 (br s, 1H), 8.75 (s, 1H), 8.63 (br s, 3H), 8.40 (d, J = 10.3 Hz, 1H), 7.16-7.06 (m, 3H), 6.96 (s, 1H), 6,82 (d, J = 8.8 Hz, 2H), 4.08-3.98 (m, 1H), 3.92-3.80 (m, 3H), 3.70 (s, 4H), 2.41- 2.19 (m, 2H), 1.63 (s, 6H)
1H NMR (400 MHz, CDCl3) δ 11.35 (br s, 1H), 8.69-8.56 (m, 1H), 8,16 (d, J = 8.1 Hz, 1H), 7.72- 7.62 (m, 1H), 7.30-7.25 (m, 2H), 7.23-7.18 (m, 2H), 6.88 (d, J = 8.8 Hz, 2H), 6.61 (s, 1H), 3.79 (s, 3H), 1.80 (s, 6H)
1H NMR (400 MHz, DMSO-d6) δ 12.43 (br s, 1 H), 9.42 (br s, 2 H), 7.79- 7.52 (m, 2 H), 7.12 (br d, J = 8.56 Hz, 2 H), 7.00 (br d, J = 8.31 Hz, 1 H), 6.92 (s, 1 H), 6.82 (br d, J = 8.56 Hz, 2 H), 4.20 (br s, 1 H), 3.74- 3.68 (m, 5 H), 3.33 (s, 7 H), 3.19 (br s, 4 H), 1.63 (s, 6 H).
1H NMR (400 MHz, DMSO-d6) δ 8.14-8.12 (m, 2H), 7.85-7.83 (m, 2H), 7.20-7.18 (m, 2H), 7.14- 7.12 (m, 2H), 7.08 (s, 1H), 4.59 (s, 2H), 3.85-3.55 (m, 8H), 3.50-3.43 (m, 2H), 2.30 (s, 3H), 1.74 (s, 6H).
1H NMR (400 MHz, CDCl3) δ 9.09-9.05 (m, 1H), 8.33-8.28 (m, 1H), 7.75 (br d, J = 8.8 Hz, 3H), 7.45-7.41 (m, 1H), 7.13- 7.08 (m, 3H), 7.06-7.02 (m, 1H), 6.61-6.57 (m, 1H), 3.83-3.77 (m, 3H), 3.64-3.55 (m, 1H), 2.45- 2.38 (m, 8H), 2.26-2.18 (m, 1H), 1.63-1.58 (m, 3H), 1.19 (s, 6H).
1H NMR (400 MHz, DMSO-d6) δ 12.06 (br s, 1H), 7.87 (d, J = 8.8 Hz, 2H), 7.12 (d, J = 8.8 Hz, 2H), 6.86 (s, 1H), 6.82 (d, J = 8.8 Hz, 2H), 6.62 (d, J = 8.8 Hz, 2H), 3.70 (s, 3H), 3.54 (t, J = 5.9 Hz, 2H), 3.16 (t, J = 5.9 Hz, 2H), 1.62 (s, 6H)
1H NMR (400 MHz, DMSO-d6) δ 12.56 (br s, 1 H), 9.61 (br s, 2 H), 8.83 (d, J = 2.8 Hz, 1 H), 8.28 (dd, J = 9.2, 2.4 Hz, 1 H), 7.45-7.38 (m, 4 H), 7.18 (s, 1 H), 7.09 (d, J = 8.8 Hz, 1 H), 3.99-3.93 (m, 4 H), 3.55 (s, 1 H), 3.18 (br s, 4 H), 1.91 (s, 3 H)
1H NMR (400 MHz, DMSO-d6) δ 12.36 (s, 1H), 9.25 (br s, 2H), 8.01 (d, J = 8.9 Hz, 2H), 7.45-7.37 (m, 4H), 7.14 (s, 1H), 7.04 (d, J = 9.1 Hz, 2H), 3.58- 3.55 (m, 4H), 3.18 (br s, 4H), 1.91 (s, 3H)
1H NMR (400 MHz, DMSO-d6) δ 12.36 (br s, 1H), 8.05 (d, J = 9.0 Hz, 2H), 7.12 (d, J = 8.8 Hz, 2H), 7.02 (d, J = 9.0 Hz, 2H), 6.91 (s, 1H), 6.82 (d, J = 8.8 Hz, 2H), 3.99-3.93 (m, 1H), 3.88 (d, J = 4.0 Hz, 2H), 3.70 (s, 3H), 1.63 (s, 6H), 1.14 (d, J = 6.3 Hz, 3H)
1H NMR (400 MHz, DMSO-d6) δ 7.66 (1H, J = 8.8 Hz, d), 7.41-7.35 (5H, m), 7.16 (1H, s), 6.91 (1H, J = 7.2 Hz, d), 3.83 (3H, s), 3.51 (1H, s), 3.01 (4H, s), 2.87 (4H, S), 1.88(3H, s)
1H NMR (400 MHz, DMSO-d6) δ 12.36 (br s, 1 H), 9.31 (br s, 2 H), 8.02 (d, J = 8.78 Hz, 2 H), 7.35- 7.47 (m, 4 H), 7.14 (s, 1 H), 7.04 (d, J = 8.78 Hz, 2 H), 3.49-3.65 (m, 5 H), 3.19 (br d, J = 4.77 Hz, 4 H), 1.91 (s, 3 H).
1H NMR (400 MHz, DMSO-d6) δ 12.36 (s, 1 H), 9.19 (br s, 2 H), 8.02 (d, J = 8.78 Hz, 2 H), 7.36-7.46 (m, 4 H), 7.15 (s, 1 H), 7.04 (d, J = 8.78 Hz, 2 H), 3.53- 3.60 (m, 5 H), 3.19 (br s, 4 H), 1.91 (s, 3 H).
1H NMR (400 MHz, CDCl3) δ 9.26 (br s, 1H), 7.78 (d, J = 8,9 Hz, 2H), 7.45 (dd, J = 5.2, 8.8 Hz, 2H), 6.99 (t, J = 8.7 Hz, 2H), 6.89-6.85 (m, 3H), 4.04-3.98 (m, 1H), 3.98- 3.89 (m, 2H), 3.66-3.54 (m, 1H), 3.53-3.46 (m, 1H), 3.43 (br d, J = 11.7 Hz, 1H), 3.20 (br d, J = 11.3 Hz,
1H NMR (400 MHz, CDCl3) δ 9.23 (br s, 1H), 7.74 (d, J = 8.9 Hz, 2H), 7.43-7.39 (m, 2H), 6.95 (t, J = 8.6 Hz, 2H), 6.86- 6.80 (m, 3H), 4.00-3.94 (m, 1H), 3.94-3,85 (m, 2H), 3.56-3.49 (m, 1H), 3.49-3.42 (m, 1H), 3.39 (br d, J = 12.2 Hz, 1H), 3.16 (br d, J = 9.5 Hz, 1H), 3.09 (br d, J = 12.0 Hz, 1H), 2.91
1H NMR (400 MHz, CDCl3) δ 9.62 (br s, 1H), 7.30 (br s, 2H), 7.07 (br s, 2H), 6.64-6.58 (m, 2H), 6.50-6.34 (m, 1H), 6.50- 6.31 (m, 3H), 4.62 (br s, 1H), 3.78 (br s, 1H), 3.64 (br s, 1H), 3.50 (br s, 1H), 3.36 (br s, 1H), 3.23 (br s, 3H), 3.00-2.56 (m, 2H), 2.27 (br s, 1H), 1.70 (br s, 3H).
1H NMR (400 MHz, CDCl3) δ 9.26 (br s, 1H), 7.76 (d, J = 8.9 Hz, 2H), 7.45-7.40 (m, 2H), 6.97 (t, J = 8.8 Hz, 2H), 6.90- 6.82 (m, 3H), 4.02-3.96 (m, 1H), 3.96-3.85 (m, 2H), 3.57-3.51 (m, 1H), 3.44-3.43 (m, 1H), 3.50- 3.43 (m, 1H), 3.40 (br d, J = 11.8 Hz, 1H), 3.17 (br d, J = 11.4 Hz, 1H), 3.10 (br d,
1H NMR (400 MHz, DMSO-d6) δ 13.06 (s, 1 H), 9.12 (br s, 2 H), 7.49- 7.43 (m, 2 H), 7.32-7.24 (m, 2 H), 7.16 (t, J = 8.8 Hz, 3 H), 3.55 (s, 1 H) 3.22, (br s, 8 H), 1.92 (s, 3 H)
1H NMR (400 MHz, DMSO-d6) δ 13.07 (s, 1 H), 9.23 (br s, 2 H), 7.49- 7.42 (m, 2 H), 7.31-7.24 (m, 2 H), 7.14 (t, J = 8.8 Hz, 3 H), 3.55 (s, 1 H), 3.22 (s, 8 H), 1.92 (s, 3 H)
1H NMR (400 MHz, DMSO-d6) δ13.05 (s, 1 H), 9.36 (br s, 2 H), 7.48- 7.37 (m, 4 H), 7.31-7.23 (m, 2 H), 7.18-7.15 (t, J = 8.8 Hz, 3 H), 3.56 (s, 1 H), 3.22 (s, 8 H), 1.90 (s, 3 H)
1H NMR (400 MHz, DMSO-d6) δ 13.05 (s, 1 H), 9.33 (br s, 2 H), 7.46- 7.37 (m, 4 H), 7.32-7.23 (m, 2 H), 7.12-7.18 (m, 1 H), 3.56 (s, 1 H), 3.22 (s, 8 H), 1.90 (s, 3 H)
1H NMR (400 MHz, DMSO-d6) δ 7.97 (d, J = 8.9 Hz, 2H), 7.45-7.37 (m, 4H), 7.12 (s, 1H), 6.94 (d, J = 9.2 Hz, 2H), 4.70 (br s, 1H), 3.85-3.70 (m, 2H), 3.53 (s, 1H), 3.41- 3.36 (m, 1H), 3.01-2.95 (m, 1H), 2.76-2.67 (m, 3H), 2.47-2.38 (m, 1H), 1.91 (s, 3H)
1H NMR (400 MHz, DMSO-d6) δ 7.97 (d, J = 8.9 Hz, 2H), 7.45-7.37 (m, 4H), 7.11 (s, 1H), 6.93 (d, J = 8.9 Hz, 2H), 4.69 (br s, 1H), 3.79 (d, J = 11.2 Hz, 1H), 3.72 (d, J = 8.2 Hz, 1H), 3.52 (s, 1H), 3.40- 3.36 (m, 2H), 3.01-2.95 (m, 1H), 2.76-2.67 (m, 3H), 2.41 (t, J = 11.0 Hz, 1H), 1.91 (s, 3H)
1H NMR (400 MHz, DMSO-d6) δ 7.97 (d, J = 8.8 Hz, 2H), 7.51-7.40 (m, 2H), 7.15 (t, J = 8.9 Hz, 2H), 7.05-6.88 (m, 3H), 4.70 (br s, 1H), 3.82- 3.65 (m, 2H), 3.49 (s, 1H), 3.41-3.37 (m, 2H), 3.04- 2.93 (m, 1H), 2.80-2.63 (m, 3H), 2.44-2.32 (m, 1H), 1.91 (s, 3H) 19F NMR (376 MHz,
1H NMR (400 MHz, DMSO-d6) δ 7.98 (d, J = 8.8 Hz, 2H), 7.49-7.36 (m, 2H), 7.15 (t, J = 8.8 Hz, 2H), 7.10 (s, 1H), 6.95 (d, J = 9.0 Hz, 2H), 4.83 (br s, 1H), 3.84-3.74 (m, 2H), 3.51 (s, 1H), 3.44- 3.41 (m, 2H), 3.05-2.99 (m, 1H), 2.82-2.73 (m, 3H), 2.49-2.48 (m, 1H), 1.91 (s, 3H)
19F NMR (376 MHz,
1H NMR (400 MHz, DMSO-d6) δ 12.59 (br s, 1H), 9.42 (br s, 2H), 8.22 (d, J = 2.0 Hz, 1H), 8.15- 8.07 (m, 1H), 7.88 (s, 1H), 7.61 (s, 1H), 7.50-7.42 (m, 2H), 7.20-7.13 (m, 4H), 3.53 (s, 1H), 3.29 (s, 4H), 3.23 (s, 4H), 1.92 (s, 3H) 19F NMR (376 MHz, DMSO-d6) δ −116.46 (s, 1F)
1H NMR (400 MHz, DMSO-d6) δ 12.77 (s, 1H), 9.81-9.64 (m, 1H), 9.61- 9.41 (m, 1H), 7.48-7.41 (m, 2H), 7.19-7.17 (m, 1H), 7.15-7.12 (m, 1H), 6.87 (s, 1H), 6.79 (d, J = 12.0 Hz, 2H), 3.98 (t, J = 15.7 Hz, 2H), 3.77-3.63 (m, 2H), 3.54 (s, 1H), 3.30-
19F NMR (376 MHz,
1H NMR (400 MHz, DMSO-d6) δ 7.52-7.36 (m, 4H), 7.16 (s, 1H), 6.63 (d, J = 12.6 Hz, 2H), 4.68 (t, J = 5.2 Hz, 1H), 3.77- 3.63 (m, 2H), 3.54 (s, 1H), 3.00-2.93 (m, 1H), 2.80- 2.63 (m, 3H), 2.47-2.29 (m, 3H), 1.90 (s, 3H) 19F NMR (376 MHz,
1H NMR (400 MHz, DMSO-d6) δ 12.74 (br s, 1H), 9.65-9.47 (m, 1H), 9.41-9.21 (m, J = 10.0 Hz, 1H), 7.34-7.30 (m, 2H), 7.12 (s, 1H), 6.87 (d, J = 8.8 Hz, 2H), 6.79 (d, J = 12.0 Hz, 2H), 3.97 (t, J = 15.1 Hz, 2H), 3.75-3.70 (m, 4H), 3.68-3.62 (m, 1H), 3.46 (s, 1H), 3.32-
19F NMR (376 MHz,
1H NMR (400 MHz, DMSO-d6) δ 12.65 (s, 1H), 8.29 (br. s, 3H), 7.46-7.37 (m, 4 H), 7.19 (s, 1H), 6.37- 6.29 (m, 2 H), 3.97 (br. s, 1H), 3.62-3.55 (m, 1 H), 3.55 (s, 1H), 3.52-3.47 (m, 1 H), 3.38-3.32 (m, 2 H), 2.37-2.26 (m, 1H), 2.16-2.05 (m, 1H), 1.90 (s, 3H).
1H NMR (400 MHz, DMSO-d6) δ 12.65 (s, 1H), 8.29 (br. s, 3H), 7.46-7.37 (m, 4 H), 7.19 (s, 1H), 6.35- 6.31 (m, 2 H), 3.96 (br. s, 1H), 3.62-3.55 (m, 1 H), 3.55 (s, 1H), 3.52-3.47 (m, 1 H), 3.38-3.32 (m, 2 H), 2.37-2.26 (m, 1H), 2.16-2.05 (m, 1H), 1.90 (s, 3H).
1H NMR (400 MHz, DMSO-d6) δ 12.64 (s, 1H), 8.28 (br. s, 3H), 7.46-7.37 (m, 4 H), 7.19 (s, 1H), 6.35- 6.31 (m, 2 H), 3.97 (br. s, 1H), 3,62-3.55 (m, 1 H), 3.55 (s, 1H), 3.52-3.47 (m, 1 H), 3.38-3.32 (m, 2 H), 2.37-2.26 (m, 1H), 2.16-2.05 (m, 1H), 1.90 (s, 3H).
1H NMR (400 MHz, DMSO-d6) δ 12.65 (s, 1H), 8.26 (br. s, 3H), 7.46-7.37 (m, 4 H), 7.19 (s, 1H), 6.35- 6.31 (m, 2 H), 3.96 (br. s, 1H), 3.62-3.55 (m, 1 H), 3.55 (s, 1H), 3.52-3.47 (m, 1 H), 3.38-3.32 (m, 2 H), 2.37-2.26 (m, 1H), 2.16-2.05 (m, 1H), 1.90 (s, 3H).
1H NMR (400 MHz, DMSO-d6) δ 12.66 (s, 1H), 8.28 (br. s, 3H), 7.50-7.40 (m, 2 H), 7.20-7.10 (m, 3H), 6.40-6.30 (m, 2 H), 3.96 (br. s, 1H), 3.61-3.55 (m, 1 H), 3.53 (s, 1H), 3.51- 3.45 (m, 1 H), 3,41-3.33 (m, 2 H), 2.35-2.27 (m, 1H), 2.15-2.07 (m, 1H), 1.91 (s, 3H).
1H NMR (400 MHz, DMSO-d6) δ 12.65 (s, 1H), 8.29 (br. s, 3H), 7.50-7.40 (m, 2 H), 7.20-7.10 (m, 3H), 6.40-6.30 (m, 2 H), 3.96 (br. s, 1H), 3.61-3.55 (m, 1 H), 3.54 (s, 1H), 3.51- 3.45 (m, 1 H), 3.41-3.33 (m, 2 H), 2.39-2.26 (m, 1H), 2.16-2.07 (m, 1H), 1.91 (s, 3H).
1H NMR (400 MHz, DMSO-d6) δ 12.66 (s, 1H), 8.25 (br. s, 3H), 7.50-7.40 (m, 2 H), 7.20-7.10 (m, 3H), 6.40-6.30 (m, 2 H), 3.96 (br. s, 1H), 3.61-3.55 (m, 1 H), 3.53 (s, 1H), 3.51- 3,45 (m, 1 H), 3.39-3.31 (m, 2 H), 2.35-2.26 (m, 1H), 2.24-2.05 (m, 1H), 1.91 (s, 3H).
1H NMR (400 MHz, DMSO-d6) δ 10.57 (br s, 1H), 7.50 (d, J = 8.6 Hz, 2H), 7.36 (d, J = 8.6 Hz, 2H), 6.90 (s, 1H), 6.28 (br s, 1H), 4.75 (t, J = 5.1 Hz, 2H), 3.60 (br. dd, J = 4.8, 8.1 Hz, 1H), 3.50 (s, 1H),
1H NMR (400 MHz, DMSO-d6) δ 10.56 (br s, 1H), 7.50 (d, J = 8.6 Hz, 2H), 7.36 (d, J = 8.6 Hz, 2H), 6.90 (s, 1H), 6.28 (br s, 1H), 4.75 (t, J = 5.1 Hz, 2H), 3.63-3.57 (m, 1H), 3.50 (s, 1H), 3.42-3.35 (m, 4H), 1.84 (s, 3H).
1H NMR (400 MHz, DMSO-d6) δ 7.66 (d, J = 8.8 Hz, 2H), 7.41-7.36 (m, J = 20.0 Hz, 4H), 7.15 (s, 1H), 6.92 (d, J = 8.0 Hz, 1H), 3.83 (s, 3H), 3.51 (s, 4H), 3.02 (s, 1H), 2.87 (s, 4H), 1.88 (s, 3H).
1H NMR (400 MHz, DMSO-d6) δ 12.72 (s, 1H), 9.37 (br s, 1H), 8.72 (br s, 1H), 7.44-7.37 (m, 4H), 7.20 (s, 1H), 6.71 (d, J = 12.5 Hz, 2H), 4.13 (br s, 1H), 3.75 (br s, 1H), 3.60 (br s, 1H), 3.58 (br s, 1H), 3.57 (br s, 1H), 3.49 (br s, 1H), 3.46 (br s, 1H), 3.33- 3.23 (m, 2H), 3.15 (br d,
1H NMR (400 MHz, DMSO-d6) δ 12.72 (s, 1H), 9.51 (br s, 1H), 8.85 (br s, 1H), 7.50-7.33 (m, 4H), 7.20 (s, 1H), 6.71 (br d, J = 12.5 Hz, 2H), 4.13 (br s, 1H), 3.83 (br d, J = 14.3 Hz, 2H), 3.74 (br dd, J = 7.8, 11.3 Hz, 1H), 3,62-3.56 (m, 1H), 3.55 (s, 1H), 3.47 (br d, J = 13.0 Hz, 1H), 3.34-
1H NMR (400 MHz, DMSO-d6) δ 7.48-7.41 (m, 1H), 7.44 (dd, J = 5.5, 8.8 Hz, 2H), 7.20-7.10 (m, 3H), 6.57 (br d, J = 13.1 Hz, 2H), 4.71 (br s, 1H), 3.76-3.65 (m, 2H), 3.52 (s, 1H), 3.48 (br d, J = 10.4 Hz, 1H), 3.12 (br d, J = 12.3 Hz, 1H), 2.96-2.90 (m,
1H NMR (400 MHz, DMSO-d6) δ 12.71 (s, 1H), 9.53 (br s, 1H), 8.87 (br s, 1H), 7.35-7.30 (m, 2H), 7.11 (s, 1H), 6.90-6.85 (m, 2H), 6.71 (br d, J = 12.4 Hz, 2H), 3.72 (s, 4H), 3.61- 3.56 (m, 1H), 3.49-3.41 (m, 2H), 3.32-3.23 (m, 2H), 3.13 (br s, 1H), 3.01
1H NMR (400 MHz, DMSO-d6) δ 12.98 (br s, 1H), 7.67 (s, 1H), 7.51- 7.40 (m, 2H), 7.33-7.09 (m, 5H), 5.80 (s, 2H), 3.59 (s, 3H), 3.54 (s, 1H), 1.92 (s, 3H).
1H NMR (400 MHz, CD3OD): δ 7.97 (br s, 1H), 7.60-7.51 (m, 4H), 7.11 (s, 1H), 7.01 (br t, J = 8.6 Hz, 2H), 3.53 (s, 3H), 2.97 (s, 1H), 1.97 (s, 3H),
1H NMR (400 MHz, CD3OD) δ 9.28 (s, 1H), 8.81 (s, 1H), 7.94 (d, J = 8.8 Hz, 2H), 7.64-7.48 (m, 2H), 7.16 (s, 1H), 7.06-6.95 (m, 2H), 4.45 (s, 2H), 2.99 (s, 1H), 2.04-1.92 (m, 3H).
1H NMR (400 MHz, DMSO-d6) δ 12.61 (br s, 2H), 8.50-8.30 (m, 2H), 7.94 (br s, 1H), 7.62 (br s, 1H), 7.47-7.44 (m, 2H), 7.42-7.38 (m, 2H), 7.17 (s, 1H), 3.55 (s, 1H), 1.92 (s, 3H)
1H NMR (400 MHz, DMSO-d6) δ 12.90- 12.70 (m, 1H), 12.62 (br d, J = 9.3 Hz, 1H), 8.49- 8.39 (m, 1H), 8.37-8.31 (m, 1H), 7.94 (ddd, J = 1.4, 8.5, 14.6 Hz, 1H), 7.74-7.59 (m, 1H), 7.47- 7.44 (m, 2H), 7.42-
1H NMR (400 MHz, DMSO-d6) δ 12.77 (s, 1 H), 9.25 (br s, 2 H), 7.33 - 7.49 (m, 4H), 7.21 (s, 1 H), 6.78 (br d, J = 12.05 Hz, 2 H), 3.52 - 3.58 (m, 5 H), 3.16 (br s, 4H), 1.90 (s, 3 H)
1H NMR (400 MHz, DMSO-d6) δ 12.62 (br s, 1H), 9.37 (br s, 2H), 7.35 - 7.11 (m, 5H),6.95 (s, 1H), 6.79 (d, J = 12.0 Hz, 2H), 4.16 (br s, 4H), 3.62 - 3.52 (m, 4H), 1.56 (d, J = 7.3 Hz, 3H)
1H NMR (400 MHz, DMSO-d6) δ 12.62 (br s, 1H), 9.43 (br s, 2 H), 7.37 - 7.31 (m, 2 H), 7.29 - 7.22 (m, 2 H), 6.97 (s, 1 H), 6.79 (br d, J = 12.0 Hz, 2 H), 4.19 (q, J = 7.2 Hz, 1 H), 3.64 - 3.54 (m, 4 H), 3.16 (br s, 4 H), 1.55 (d, J = 7.2 Hz, 3 H)
1H NMR (400 MHz, DMSO-d6) δ 12.64 (br. s, 1H), 9.46 (s,1H), 7.28 - 7.20 (m. 2H), 7.18 - 7.16 (m. 2H), 6.98 (s,1H), 6.79 - 6.76 (m, 2H), 3.84 (s,2H), 3.59 - 3.56 (m, 4H), 3.26 (s, 3H), 3.16 - 3.14 (m, 4H), 1.67 (s, 3H).
1H NMR (400 MHz, DMSO-d6) δ 12.65 (s, 1 H), 9.01 (s, 2 H), 7.27 - 7.20 (m, 2 H), 7.11 - 7.04 (m, 2 H), 6.79 (s, 1 H), 6.76 (d, 1 H), 3.58 - 3.52 (m, 4 H), 3.20 - 3.12 (m, 4 H), 1.62 (s, 6H)
1H NMR (400 MHz, DMSO-d6) δ 7.42 (d, 2 H), 7.22 (d, 2 H), 7.04 (s, 1 H), 6.62 (s, 2 H), 3.18 (t, 4 H), 2.76 (t, 4 H), 2.45 (t, 4 H), 2.02 (t, 2 H), 1.62 (t, 2 H)
1H NMR (400 MHz, DMSO-d6) δ 12.75 (s, 1 H), 9.42 (br. s, 2 H), 7.45 - 7.35 (m, 4 H), 7.20 (s, 1 H), 6.79 (s, 1 H), 6.76 (s, 1 H), 3.60 - 3.55 (m, 4 H), 3.54 (s, 1 H), 2.51 - 2.49 (m, 4H), 1.90 (s, 3 H)
1H NMR (400 MHz, DMSO-d6) δ 12.75 (s, 1 H), 9.47 (br. s, 2 H), 7.46 - 7.36 (m, 4 H), 7.20 (s, 1 H), 6.79 (s, 1 H), 6.76 (s, 1 H), 3.61 - 3.55 (m, 4 H), 3.54 (s, 1 H), 3.19 - 3.11 (m, 4H), 1.89 (s, 3 H)
1H NMR (400 MHz, DMSO-d6) δ 2.76 (s, 1H), 7.34-7.47 (m, 4H), 7.20 (s, 1H), 6.75 (br d, J = 12.2 Hz, 2H), 3.56-3.66 (m, 2H), 3.54 (s, 1H), 3.42-3.52 (m, 2H), 2.99-3.16 (m, 4H), 2.74 (s, 3H), 1.90 (s, 3H).
1H NMR (400 MHz, DMSO-d6) δ 12.79 (s, 1 H), 10.96 (br. s, 1 H), 7.45 - 7.35 (m, 4 H), 7.21 (s, 1 H), 6.82 (s, 1 H), 6.79 (s, 1 H), 4.09 - 4.00 (m, 2 H), 3.58 (s, 1 H), 3.49- 3.40 (m, 2 H), 3.30 - 3.20 (m, 2 H), 3.13 - 3.01 (m, 2H), 2.82 -
1H NMR (400 MHz, DMSO-d6) δ 12.79 (s, 1 H), 11.02 (br. s, 1 H), 7.47 - 7.35 (m, 4 H), 7.21 (s, 1 H), 6.82 (s, 1 H), 6.79 (s, 1 H), 4.09 - 4.00 (m, 2 H), 3.56 (s, 1 H), 3.49- 3.40 (m, 2 H), 3.32 - 3.20 (m, 2 H), 3.13 - 3.01 (m, 2H), 2.82 -
1H NMR (400 MHz, DMSO-d6) δ 7.22-7.18 (m, 5H), 6.89 (s, 1H), 6.61 (d, J = 12 Hz, 2H), 3.83 (s, 2H), 3.42-3.40 (m, 2H), 3.14 (t, 4H), 2.73 (t, 4H), 1.64 (s, 3H), 1.01 (s, 3H).
1H NMR (400 MHz, DMSO-d6) δ 12.80 (s, 1 H), 7.81 (d, 2 H), 7.07 (d, 2 H), 7.03 (s, 2 H), 6.74 (s, 1 H), 3.81 (s, 2 H), 3.23 (s, 3 H), 3.18 (t, 4 H), 2.76 (t, 4 H), 1.72 (s, 3 H)
1H NMR (400 MHz, DMSO-d6) δ 7.42 (d, J = 8 Hz, 2H), 7.20 (d, J = 4 Hz, 2H), 7.03 (s, 1H), 6.65 (d, J = 12 Hz, 2H), 3.38 (s, 4H), 2.35 (s, 4H), 2.17 (s, 3H), 2.01 (s, 4H), 1.62 (d, J = 8 Hz, 4H).
1H NMR (400 MHz, DMSO-d6) δ 12.64 (s, 1 H), 9.39 (s, 2 H), 7.34 - 7.29 (m, 2 H) 7.22 - 7.19 (m, 2 H), 6.99 (s, 1 H), 6.78 (d, J = 12.0 Hz, 2 H), 3.80 - 3.77 (m, 2 H), 3.60 - 3.55 (m, 4 H) 3.1 (s, 3 H) 3.18 - 3.12 (m, 4 H), 1.65 (s, 3 H)
1H NMR (400 MHz, DMSO-d6) δ 7.30 - 7.20 (m, 5H), 6.96 (s, 1H), 6.70 - 6.60 (m, 2H), 3.84 (s, 2H), 3.27 (s, 3H), 3.25 - 3.17 (m, 3H), 2.83 - 2.75 (m, 3H), 1.67 (s, 3H)
1H NMR (400 MHz, DMSO-d6) δ 7.29 - 7.23 (m, 2H), 7.21 - 7.13 (m, 3H), 6.98 (s, 1H), 6.79 - 6.72 (m, 2H), 3.84 (s, 2H), 3.50 - 3.44 (m, 4H), 3.26 (s, 3H), 3.12 - 3.06 (m, 4H), 1.67 (s, 3H)
1H NMR (400 MHz, DMSO-d6) δ 13.07 (s, 1 H), 9.16 (s, 2 H), 7.41 (s, 4 H), 6.83 (d, J = 12.4 Hz, 2 H), 3.63 (s, 1 H), 3.62 - 3.57 (m, 4 H), 3.19 (br s, 4 H), 1.94 (s, 3 H).
1H NMR (400 MHz, DMSO-d6) δ 13.07 (s, 1 H), 9.23 (s, 2 H), 7.41 (s, 4 H), 6.83 (d, J = 12.4 Hz, 2 H), 3.63 (s, 1 H), 3.62 - 3.57 (m, 4 H), 3.19 (br s, 4 H), 1.94 (s, 3 H)
1H NMR (400 MHz, DMSO-d6) δ 12.68 (br., s, 1H), 7.42 -7.39 (m, 4 H), 7.18 (s, 1 H), 6.67 - 6.65 (m, 2 H), 4.51 - 4.48 (m, 1 H), 3.53 (s, 1 H), 3.30 - 3.22 (m, 2 H), 2.44 - 2.39 (m, 2 H), 1.89 (s, 3 H).
1H NMR (400 MHz, DMSO-d6) δ 12.68 (br., s, 1H), 7.50 -7.40 (m, 4 H), 7.19 (s, 1 H), 6.73 - 6.62 (m, 2 H), 4.60 (br., s, 1H), 3.53 (s, 1 H), 3.35 - 3.25 (m, 4 H), 2.73 - 2.50 (m, 6 H), 1.90 (s, 3 H).
1H NMR (400 MHz, DMSO-d6) δ 12.64 (s, 1 H), 9.41 (s, 2 H), 7.32 (d, J = 8.4 Hz, 2 H) 7.22 (d, J = 8.8 Hz, 2 H), 6.99 (s, 1 H), 6.78 (d, J = 12.0 Hz, 2 H), 3.87 - 3.78 (m, 2 H) 3.62 - 3.55 (m, 4 H), 3.26 (s, 3 H), 3.20 - 3.13 (m, 4 H), 1.66 (s, 3 H)
1H NMR (400 MHz, DMSO-d6) δ 12.64 (s, 1 H), 9.42 (s, 2 H), 7.32 (d, J = 8.4 Hz, 2 H) 7.21 (d, J = 8.8 Hz, 2 H), 6.99 (s, 1 H), 6.78 (d, J = 12.0 Hz, 2 H), 3.87 - 3.76 (m, 2 H) 3.58 - 3.56 (m, 4 H), 3.26 (s, 3 H) 3.20 - 3.13 (m, 4 H), 1.65 (s, 3 H)
1H NMR (400 MHz, DMSO-d6) δ 7.42 (m, 2 H), 7.22 (m, 2 H), 7.04 (s, 1 H), 6.62 (d, J = 8.9 Hz, 2 H), 3.18 (m, 4 H), 2.76 (m, 4 H), 2.45 (s, 1 H), 2.02 (m, 2 H), 2.01 (s, 1 H), 1.62 (m, 4 H)
1H NMR (400 MHz, DMSO-d6) δ 7.42 (d, J = 8.0 Hz, 2H), 7.22 (d, J = 8.0 Hz, 2H), 7.03 (s, 1H), 6.66 (d, J = 12.0 Hz, 2H), 3.26 (s, 4H), 2.36 (s, 4H), 2.17 (s, 3H), 2.02 (s, 4H), 1.61 (s, 4H).
1H NMR (400 MHz, DMSO-d6) δ 7.24-7.12 (m, J = 48.0 Hz, 5H), 6.93 (s, 1H), 6.62 (d, J = 12.0 Hz, 2H), 3.84 (s, 2H), 3.42 (q, J = 16.0 Hz, 2H), 3.17 (s, 4H), 2.75 (s, 4H), 1.64 (s, 3H), 1.05 (t, J = 12.0 Hz, 3H).
1H NMR (400 MHz, DMSO-d6) δ 7.27-7.13 (m, J = 56.0 Hz, 5H), 6.89 (s, 1H), 6.66 (d, J = 12.0 Hz, 2H), 3.81 (s, 2H), 3.28 (s, 4H), 3.26 (s, 3H), 2.40-2.37 (m, 4H), 2.17 (s, 3H), 1.64 (s, 3H).
1H NMR (400 MHz, DMSO-d6) δ 12.76 (s, 1 H), 9.28 (br s, 2 H), 7.44 (dd, J = 8.91, 5.40 Hz, 2 H), 7.09 - 7.20 (m, 3 H), 6.78 (br d, J = 12.05 Hz, 2 H), 3.54 - 3.62 (m, 4 H), 3.53 (s, 1 H), 3.16 (br s, 4 H), 1.90 (s, 3 H).
1H NMR (400 MHz, DMSO-d6) δ 12.76 (s, 1 H), 9.57 (br s, 2 H), 7.39 - 7.49 (m, 2 H), 7.09 - 7.20 (m, 3 H), 6.77 (br d, J = 12.30 Hz, 2 H), 3.54 - 3.65 (m, 4 H), 3.53 (s, 1 H), 3.15 (br s, 4 H),
1H NMR (400 MHz, DMSO-d6) δ 12.76 (s, 1H), 8.89 (br s, 2H), 7.32 (d, J = 8.8 Hz, 2H), 7.12 (s, 1H), 6.87 (d, J = 9.0 Hz, 2H), 6.79 (d, J = 12.1 Hz, 2H), 3.72 (s, 3H), 3.56 - 3.52 (m, 4H), 3.47 (s, 1H), 3.18 (br s, 4H), 1.88 (s, 3H).
1H NMR (400 MHz, DMSO-d6) δ 12.77 (s, 1 H), 9.25 (br s, 2 H), 7.56 (t, J = 8.17 Hz, 1 H), 7.42 (dd, J = 10.85, 2.15 Hz, 1 H), 7.28 (dd, J = 8.46, 1.91 Hz, 1 H), 7.23 (s, 1 H), 6.79 (br d, J = 12.16 Hz, 2 H), 3.62 (s, 1 H), 3.50 - 3.60 (m, 4 H), 3.17 (br s, 4 H), 1.91 (s, 3 H).
1H NMR (400 MHz, DMSO-d6) δ 12.76 (s, 1 H), 9.12 (br s, 2 H), 7.56 (t, J = 8.16 Hz, 1 H), 7.42 (dd, J = 10.79, 2.01 Hz, 1 H), 7.28 (br d, J = 8.78 Hz, 1 H), 7.23 (s, 1 H), 6.79 (br d, J = 12.05 Hz, 2 H), 3.61 (s, 1 H), 3.53 - 3.59 (m, 4 H), 3.17 (br s, 4 H), 1.92 (s, 3 H).
1H NMR (400 MHz, DMSO-d6) δ 12.76 (br s, 1H), 9.42 (br s, 2H), 7.45 - 7.40 (m, 2H), 7.40 - 7.35 (m, 2H), 7.17 (s, 1H), 6.78 (d, J = 12.3 Hz, 2H), 3.65 - 3.52 (m, 4H), 3.23 - 3.10 (m, 4H), 1.89 (s, 3H), 1.87 (s, 3H)
1H NMR (400 MHz, DMSO-d6) δ 7.30 (d, J = 8.1 Hz, 2H), 7.16 - 7.07 (m, 3H), 6.71 (br d, J = 12.4 Hz, 2H), 3.47 (s, 1H), 3.39 - 3.34 (m, 4H), 3.00 - 2.89 (m, 4H), 2.25 (s, 3H), 1.88 (s, 3H).
1H NMR (400 MHz, DMSO-d6) δ 7.30 (d, J = 8.1 Hz, 2H), 7.13 - 7.10 (m, 3H), 6.64 (d, J = 12.6 Hz, 2H), 3.45 (s, 1H), 3.24 - 3.13 (m, 6H), 2.78 - 2.75 (m, 4H), 2.26 (s, 3H), 1.88 (s, 3H).
1H NMR (400 MHz, DMSO-d6) δ 12.76 (br s, 1H), 9.52 (br s, 2H), 7.47 - 7.41 (m, 4H), 7.21 (s, 1H), 6.77 (br d, J = 12.1 Hz, 2H), 4.16 (s, 1H), 3.58 (br s, 4H), 3.15 (br s, 4H), 1.90 (s, 3H).
1H NMR (400 MHz, DMSO-d6) δ 12,75 (s, 1 H), 9.18 (br s, 2 H), 7.67 (t, J = 8.8 Hz, 1 H), 7.39 - 7.29 (m, 2 H), 7.19 (s, 1 H), 6.78 (br d, J = 12.0 Hz, 2 H), 3.59 (s, 1 H), 3.58 - 3.55 (m, 4 H), 3.17 (br s, 4 H), 1.94 (s, 3 H)
1H NMR (400 MHz, DMSO-d6) δ 12.76 (s, 1 H), 9.14 (br s, 2 H), 7.67 (t, J = 8.8 Hz, 1 H), 7.38 - 7.31 (m, 2 H), 7.20 (s, 1 H), 6.78 (d, J = 12.4 Hz, 2 H), 3.60 (s, 1 H) 3.58 - 3.53(m, 4 H), 3.18 (br s, 4 H), 1.95 (s, 3 H)
1H NMR (400 MHz, DMSO-d6) δ 12.61 (s, 1 H), 9.26 (br s, 2 H), 7.34 - 7.29 (m, 2 H), 7.20 (d, J = 8.8 Hz, 2 H), 7.14 (s, 1 H), 6.77 (d, J = 12.4 Hz, 2 H), 3.62 - 3.49 (m, 4 H), 3.16 (br s, 4 H), 1.53- 1.46 (m, 1 H), 1.42 (s, 3 H) 0.58 - 0.51 (m,
1H NMR (400 MHz, DMSO-d6) δ 12.70 (s, 1 H), 9.21 (br s, 2 H), 7.37 - 7.28 (m, 4 H), 7.25 - 7.20 (m, 1 H), 7.15 - 7.08 (m, 4 H), 6.79 (d, J = 12.0 Hz, 2 H), 6.60 (s, 1 H) 3.60 - 3.56 (m, 4 H), 3.17 (br s, 4 H) 2.07 (s, 3 H)
1H NMR (400 MHz, DMSO-d6) δ 12.75 (s, 1H), 9.23 (br s, 2H), 7.49 - 7.43 (m, 2H), 7.41 - 7.36 (m, 2H), 7.21 (s, 1H), 6.78 (d, J = 12.0 Hz, 2H), 3.61 (s, 1H), 3.59 - 3.53 (m, 4H), 3.17 (s, 4H), 2.40 - 2.30 (m, 1H), 2.23 - 2.14 (m, 1H), 0.88 - 0.81 (m, 3H). 19F NMR (376 MHz, DMSO-d6) δ −111.77 (s, 2F)
1H NMR (400 MHz, DMSO-d6) δ 12.75 (s, 1H), 9.55 (br s, 2H), 7.32 - 7.27 (m, 2H), 7.11 (s, 1H), 6.87 - 6.82 (m, 2H), 6.79 - 6.71 (m, 2H), 3.71 (s, 3H), 3.60 - 3.52 (m, 4H), 3.46 (s, 1H), 3.16 - 3.07 (br s, 4H), 1.88 (s, 3H).
1H NMR (400 MHz, DMSO-d6) δ 13.07 (s, 1 H), 9.16 (br s, 2 H), 7.41 (s, 4 H), 6.83 (d, J = 12.4 Hz, 2 H), 3.63 (s, 1 H), 3.62 - 3.57 (m, 4 H), 3.19 (br s, 4 H), 1.94 (s, 3 H)
1H NMR (400 MHz, DMSO-d6) δ 13.07 (br s, 1 H), 9.23 (br s, 2 H), 7.41 (s, 4 H), 6.83 (br d, J = 12.4 Hz, 2 H), 3.63 (s, 1 H) 3.62 - 3.57 (m, 4 H), 3.19 (br s, 4 H), 1.94 (s, 3 H)
1H NMR (400 MHz, CD3OD-d6) δ 7.64 (s, 1H), 7.58 (br d, J = 8.0 Hz, 2H), 7.39 - 7.29 (m, 2H), 6.72 (br d, J = 11.8 Hz, 2H), 3.65 - 3.54 (m, 4H), 3.42 - 3.35 (m, 4H), 2.98 (s, 1H), 1.90 (s, 3H)
1H NMR (400 MHz, CD3OD-d6) δ 7.52 (br d, J = 8.4 Hz, 2H), 7.40 (br d, J = 8.4 Hz, 2H), 7.22 (s, 1H), 6.76 (br d, J = 12.4 Hz, 2H), 3.65 - 3.59 (m, 4H), 3.39 - 3.32 (m, 4H), 3.20 (s, 1H), 1.97 (s, 3H)
1H NMR (400 MHz, DMSO-d6) δ 12.00 (s, 1H), 7.40 (d, J = 8.6 Hz, 2H), 7.11 (d, J = 8.5 Hz, 2H), 6.87 (s, 1H), 2.02 (s, 3H), 1.57 (s, 6H).
1H NMR (400 MHz, DMSO-d6) δ 12.15 (s, 1 H), 7.30 (d, J = 8.8 Hz, 2 H), 6.99 (s, 1 H), 6.86 (d, J = 8.8 Hz, 2 H), 3.71 (s, 3 H), 3.42 (s, 1 H), 2.06 (s, 3 H), 1.85 (s, 3 H).
1H NMR (400 MHz, DMSO-d6) δ 12.14 (s, 1H), 7.59 (t, J = 8.4 Hz, 1H), 7.45 (d, J = 9.5 Hz, 2H), 7.09 - 7.06 (m, 1H), 3.58 - 3.54 (m, 1H), 2.07 (s, 3H), 1.92 (s, 3H)
1H NMR (400 MHz, CDCl3) δ 9.98 (br s, 1H), 7.45 (d, J = 8.5 Hz, 2H), 7.30 (d, J = 8.5 Hz, 2H), 6.88 (s, 1H), 2.63 (s, 1H), 2.25 (s, 3H), 1.99 (s, 3H)
1H NMR (400 MHz, CDCl3) δ 8.67 (br s, 1 H), 7.42 - 7.45 (m, 2 H), 7.34 - 7.38 (m, 2 H), 6.90 (s, 1 H),3.70 (br d, J = 3.6 Hz, 2 H), 3.11 - 3.20 (m, 1 H), 2.56 - 2.64 (m, 2 H) 2.45 - 2.53
1H NMR (400 MHz, CDCl3) δ 13.28 (s, 1 H), 7.48 - 7.56 (m, 4 H), 6.91 (s, 1 H), 3.65 (d, J = 4.4 Hz, 2 H), 3.32 (t, J = 7.6 Hz, 1 H), 2.78 (s, 1 H), 2.65 - 2.55 (m, 1 H), 2.43 - 2.52 (m, 2
1H NMR (400 MHz, DMSO-d6) δ 12.10 (s, 1 H) 7.48 - 7.54 (m, 2 H) 7.34 (d, J = 8.53 Hz, 2 H) 7.09 (s, 1 H) 5.19 (d, J = 7.03 Hz, 1 H) 3.90 - 4.01 (m, 1 H) 3.51 (s, 1 H) 3.33 (s, 3 H) 2.63 - 2.71 (m,
1H NMR (400 MHz, CDCl3) δ 8.77 (s, 1 H), 7.45 - 7.38, (m, 4 H), 6.95 (s, 1 H), 2.63 (s, 1 H), 2.43 - 2.34(m, 1 H), 2.24- 2.14 (m, 4 H), 0.93 (t, J = 7.2 Hz, 3 H)
1H NMR (400 MHz, CDCl3) δ 8.79 (br s, 1H), 7.46 - 7.39 (m, 2H), 7.39 - 7.31 (m, 2H), 6.90 (s, 1H), 2.58 (s, 1H), 2.20 (s, 3H), 1.95 (s, 3H)
1H NMR (400 MHz, CDCl3) δ 8.74 (br s, 1H), 7.51 - 7.40 (m, 2H), 7.40 - 7.31 (m, 2H), 6.90 (s, 1H), 2.58 (s, 1H), 2.21 (s, 3H), 1.95 (s, 3H)
1H NMR (400 MHz, CDCl3) δ 8.78 (br s, 1H), 7.48 - 7.40 (m, 2H), 7.39 - 7.30 (m, 2H), 6.90 (s, 1H), 2.58 (s, 1H), 2.21 (s, 3H), 1.95 (s, 3H)
Step 1. Preparation of compound 6-chloro-N-(4-(2-(4-methoxyphenyl)propan-2-yl)thiazol-2-yl)nicotinamide
A mixture of compound 4-(2-(4-methoxyphenyl)propan-2-yl)thiazol-2-amine (100 mg, 0.35 mmol, HCl salt), compound 6-chloronicotinic acid (83.0 mg, 0.53 mmol) and EDCI (135 mg, 0.70 mmol) in pyridine (3 mL) was stirred at 80° C. for 2 h. The reaction mixture was concentrated. The residue was purified by silica gel chromatography (PE:EA=2:1). Desired compound (63 mg, 46.26% yield) was obtained as yellow oil.
MS (ESI) m/z (M+H)+=388.0
Step 2. Preparation of compound 6-((2-(dimethylamino)ethyl)amino)-N-(4-(2-(4-methoxyphenyl)propan-2-yl)thiazol-2-yl)nicotinamide
A mixture of compound obtained from step 1 above (63 mg, 0.16 mmol), N,N-dimethylethane-1,2-diamine (43.0 mg, 0.49 mmol) and DIEA (84.0 mg, 0.65 mmol) in DMF (5 mL) was stirred at 65° C. for 16 h. The reaction mixture was concentrated. The residue was purified prep-HPLC (water (0.05% HCl)-ACN]). The desired compound (25.01 mg, 35.0% yield) was obtained as a yellow solid.
1H NMR (400 MHz, MeOD) δ 8.43-8.32 (m, 1H), 8.18-8.11 (m, 1H), 7.35 (s, 1H), 7.23-7.14 (m, 3H), 6.83 (d, J=8.8 Hz, 2H), 6.79 (s, 1H), 3.76 (m, 4H), 1.70 (s, 6H).
MS (ESI) m/z (M+H)+=440.2
To a solution of compound 6-(piperazin-1-ylmethyl)-N-(4-(2-(p-tolyl)propan-2-yl)thiazol-2-yl)nicotinamide (0.03 g, 69 μmol, 1 eq) in CH3CN (10 mL) was added 2-bromoethanol (9.47 mg, 76 μmol, 5 μL, 1.1 eq) and K2CO3 (19 mg, 137.8 μmol, 2 eq). Then the reaction mixture was stirred at 80° C. for 16 hr. The reaction was concentrated under reduced pressure to afford a residue. The residue was purified by prep-HPLC (water (0.225% FA)-ACN]; B %: 15%-45%, 7.5 min). Compound (2.3 mg, yield: 6.9%) was obtained as a white solid.
1H NMR (400 MHz, CDCl3) δ 9.09-9.05 (m, 1H), 8.33-8.28 (m, 1H), 7.75 (br d, J=8.8 Hz, 3H), 7.45-7.41 (m, 1H), 7.13-7.08 (m, 3H), 7.06-7.02 (m, 1H), 6.61-6.57 (m, 1H), 3.83-3.77 (m, 3H), 3.64-3.55 (m, 1H), 2.45-2.38 (m, 8H), 2.26-2.18 (m, 1H), 1.63-1.58 (m, 3H), 1.19 (s, 6H). MS (ESI) m/z (M+H)+=480.3.
Step 1. Preparation of compound methyl 3-(((tert-butyldiphenylsilyl)oxy)methyl) cyclobutanecarboxylate
To a solution of methyl 3-(hydroxymethyl)cyclobutanecarboxylate (200 mg, 1.39 mmol) and imidazole (189 mg, 2.77 mmol) in DCM (5 mL) was added TBDPSCl (458 mg, 1.66 mmol, 427 μL) at 25° C. The solution was stirred for 12 h at 25° C. The mixture was diluted with DCM (30 mL), washed with H2O (3×10 mL), brine (10 mL), dried over anhydrous Na2SO4, filtered and concentrated in vacuum to give a residue. The residue was purified by silica column (ethyl acetate in petroleum ether=0-20%). The desired compound (420 mg, yield: 79.1%) was obtained as a yellow oil.
MS (ESI) m/z (M+H)+=383.1
Step 2. Preparation of compound 3-(((tert-butyldiphenylsilyl)oxy)methyl) cyclobutanecarboxylic acid
To mixture of compound obtained from step 1 above (412 mg, 1.08 mmol) in THF (1.5 mL)/MeOH (0.5 mL)/H2O (0.5 mL) was added LiOH·H2O (90.6 mg, 2.16 mmol) at 0° C. The mixture was stirred for 3 h at 25° C. The mixture was diluted with H2O (15 mL), adjusted pH=6-7, extracted with EA (15 mL×3). The combined organic layers were washed with brine (10 mL), dried over anhydrous Na2SO4, filtered and concentrated in vacuum to give a residue. The desired compound (413 mg, crude) was obtained as a yellow solid. The crude product was directly used for next step without further purification
MS (ESI) m/z (M+Na)*=391.1
Step 3. Preparation of compound methyl 2-(4-bromophenyl)-2-(2-((1R, 3R)-3-(((tert-butyldiphenylsilyl)oxy)methyl)cyclobutanecarboxamido)thiazol-4-yl)propanoate
To solution of compound obtained from step 2 above (410 mg, 1.11 mmol) and DIPEA (173 mg, 1.34 mmol, 233 μL) in DCM (5 mL) was stirred for 10 min at 20° C. Methyl 2-(2-aminothiazol-4-yl)-2-(4-bromophenyl)propanoate (152 mg, 446 μmol) and PyBOP (580 mg, 1.11 mmol) was added at 20° C. The mixture was stirred for 12 h at 20° C. The mixture was diluted with DCM (30 mL), washed with H2O (10 mL), brine (10 mL), dried over anhydrous Na2SO4, filtered and concentrated in vacuum to give a residue. The residue was purified by silica column (ethyl acetate in petroleum ether=0-20%). The desired compound A (194 mg, crude) was obtained as a yellow oil. The other desired compound B (186 mg, crude) obtained as a yellow oil. The crude product was directly used for next step without further purification. The chiral of the products were confirmed in the final step.
Step 4. Preparation of compound (1R, 3R)-N-(4-(2-(4-bromophenyl)-1-hydroxypropan-2-yl)thiazol-2-yl)-3-(((tert-butyldiphenylsilyl)oxy)methyl)cyclobutanecarboxamide
To a solution of compound obtained from step 3 above (194 mg, 280.4 ρmol) in THF (5 mL) was added LiBH4 (31 mg, 1.40 mmol) at 20° C. The mixture was stirred at 20° C. for 12 h. The mixture was quenched with sat. NH4Cl aq (10 mL), diluted with H2O (20 mL) and extracted with EA (20 mL×3). The organic layer was washed with brine (10 mL), dried over anhydrous Na2SO4, filtered and concentrated in vacuum to give a residue. The residue was purified by silica column (ethyl acetate in petroleum ether=0-30%). The desired compound (77 mg, yield: 41.4%) was obtained as a yellow oil.
MS (ESI) m/z (M+H)+=663.1
Step 5. Preparation of compound (1R, 3R)-N-(4-(2-(4-bromophenyl)-1-oxopropan-2-yl)thiazol-2-yl)-3-(((tert-butyldiphenylsilyl)oxy)methyl)cyclobutanecarboxamide
To a mixture of Dess-Martin (73 mg, 171.2 ρmol, 53 μL) in DCM (2 mL) was added the solution of compound obtained from step 4 above (77 mg, 132 ρmol) in DCM (2 mL) at 20° C. The mixture was stirred for 3 h at 20° C. The mixture was quenched with sat. NaHCO3 (10 mL)/sat Na2S2O4 (10 mL), extracted with DCM (15 mL×3). The combined organic layers were washed with brine (10 mL), dried over anhydrous Na2SO4, filtered and concentrated in vacuum to give a residue. The desired compound (77 mg, crude) was obtained as a yellow solid. The crude product was directly used for next step without further purification.
Step 6. Preparation of compound (1R, 3R)-N-(4-(2-(4-bromophenyl)but-3-yn-2-yl)thiazol-2-yl)-3-(((tert-butyldiphenylsilyl)oxy)methyl)cyclobutanecarboxamide
To a solution of compound obtained from step 5 above (77 mg, 116 ρmol), 1-diazo-1-dimethoxyphosphoryl-propan-2-one (34 mg, 174.5 ρmol) and K2CO3 (32 mg, 232.7 ρmol) in MeOH (2 mL) was stirred for 12 h at 20° C. The mixture was concentrated in vacuum to give a residue. The residue was purified by silica column (ethyl acetate in petroleum ether=0-15%). The desired compound (37 mg, yield: 48.3%) was obtained as a yellow oil.
MS (ESI) m/z (M+H)+=657.1
Step 7. Preparation of compound (1R, 3R)-N-(4-(2-(4-bromophenyl)but-3-yn-2-yl)thiazol-2-yl)-3-(hydroxymethyl)cyclobutanecarboxamide
To a solution of compound obtained from step 6 above (37 mg, 56.3 ρmol) in THF (2 mL) was added TBAF (1 M, 0.1 mL) at 20° C. The mixture was stirred for 12 h at 20° C. The mixture was diluted with EA (50 mL), washed with H2O (10 mL×3), brine (10 mL), dried over anhydrous Na2SO4, filtered and concentrated in vacuum to give a residue The residue was purified by silica column (ethyl acetate in petroleum ether=0-15%). The desired compound (12.61 mg, yield: 53.5%) was obtained as a yellow solid.
1H NMR (400 MHz, CDCl3) δ 13.28 (br s, 1H), 7.56-7.48 (m, 4H), 6.91 (s, 1H), 3.65 (d, J=4.4 Hz, 2H), 3.34-3.30 (m, 1H), 2.77 (s, 1H), 2.63-2.61 (m, 1H), 2.52-2.43 (m, 2H), 2.34-2.32 (m, 2H), 2.15 (s, 3H). MS (ESI) m/z (M+H)=419.0.
The other isomer was synthesized using the similar procedure above.
To a solution of compound 4-formyl-N-(4-(2-(4-methoxyphenyl)propan-2-yl)thiazol-2-yl)benzamide (120 mg, 0.32 mmol) and 2-(piperazin-1-yl)ethan-1-ol (42 mg, 0.32 mmol) in DCM (5 mL) was added NaBH3CN (59 mg, 0.95 mmol) and HOAc (2 drops). The mixture was stirred at r.t overnight. The reaction mixture was concentrated to give a residue. The residue was purified by flash silica gel chromatography (DCM:MeOH=1:0 to 10:1). The desired compound (80 mg, yield: 51.4%) was obtained as a white solid.
MS (ESI) m/z (M+H)+=495.2
ALPK1 is an intracytoplasmic serine threonine protein kinase that plays an important role in activating the innate immune response. ALPK1 binds to the bacterial pathogen-associated molecular pattern metabolite (PAMP), ADP-D-glycero-beta-D-manno-heptose (ADP-heptose). ALPK1-ADP-heptose binding occurs through direct interaction at the ALPK1 N-terminal domain. This interaction stimulates the kinase activity of ALPK1 and its phosphorylation and activation of TRAF-interacting protein with forkhead-associated domain (TIFA). In turn, TIFA activation triggers proinflammatory NFkB signaling, including proinflammatory cytokine and chemokine expression and/or secretion. Accordingly, the compounds disclosed herein are generally useful as inhibitors of ALPK1 kinase activity and downstream activation of NFkB proinflammatory signaling.
The disclosure provides for the use of a compound of Formula I, or a subembodiment thereof as described herein, for inhibiting ALPK1 kinase activity and reducing inflammation in a target tissue. The methods also encompass the use of a compound of Formula I, or a subembodiment thereof as described herein, for treating a disease, disorder, or condition characterized by excessive or inappropriate ALPK1-dependent proinflammatory signaling. In embodiments, the disease, disorder, or condition is selected from sepsis, cancer, spiroandenoma, spiroandenocarcinoma, “Retinal dystrophy, Optic nerve edema, Splenomegaly, Anhidrosis and migraine Headache” (“ROSAH”) syndrome, and “Periodic Fever, Aphthous Stomatitis, Pharyngitis, and Adenitis” (“PFAPA”) syndrome. In embodiments, the cancer is selected from lung cancer, colon cancer, and oral squamous cancer. In embodiments, the cancer is oral squamous cancer.
In embodiments, the disclosure provides methods for inhibiting ALPK1 kinase activity in a mammalian cell or target tissue by contacting the cell or target tissue with a compound of Formula I, or a subembodiment described herein. In embodiments, the methods comprise administering a pharmaceutical composition comprising a compound of Formula I, or a subembodiment described herein, to a subject in an amount effective to inhibit ALPK1 kinase activity in a target cell or tissue of the subject. In embodiments, the methods comprise reducing inflammation in a target tissue of a subject in need of such therapy by administering to the subject a compound of Formula I, or a subembodiment described herein, or a pharmaceutical composition comprising same.
In embodiments, the disclosure provides methods of treating a subject having a disease or disorder characterized by excessive or inappropriate activation of ALPK1 kinase activity, the methods comprising administering to the subject a compound of Formula I, or a subembodiment described herein. In embodiments, the disease or disorder is selected from sepsis, cancer, spiroandenoma, spiroandenocarcinoma, ROSAH syndrome, and PFAPA syndrome.
In embodiments, the disease or disorder is spiradenoma or spiroandenocarcinoma, and the methods comprise administering a compound of Formula I, or a subembodiment described herein, to a subject in need of such treatment. In embodiments, the subject in need of treatment is one diagnosed with spiradenoma or spiroandenocarcinoma and carrying one or more genetic mutations in ALPKL. In embodiments, at least one of the genetic mutations is an activating mutation. In embodiments, the genetic mutation in ALPK1 is p.V1092A, as described in Rashid et al., Nature Communications (2019).
In embodiments, the disease or disorder is ROSAH, and the methods comprise administering a compound of Formula I, or a subembodiment described herein, to a subject in need of such treatment. In embodiments, the subject in need of treatment is one diagnosed with ROSAH and carrying one or more genetic mutations in ALPK1. In embodiments, at least one of the genetic mutations is an activating mutation. In embodiments, the genetic mutation in the ALPK1 gene is c.710C>T, p.T237M, as described in Williams et al., Genetics in Medicine 21:2103-2115 (2019).
In embodiments, the disease or disorder is PFAPA, and the methods comprise administering a compound of Formula I, or a subembodiment described herein, to a subject in need of such treatment. In embodiments, the subject in need of treatment is one diagnosed with or having clinical symptoms of PFAPA and carrying one or more genetic mutations in ALPK1. In embodiments, at least one of the genetic mutations is an activating mutation. In embodiments, the genetic mutation in the ALPK1 gene is 2770T>C, p.(S924P), as described in Sangiorgi et al. Eur. J. Human Genetics (2019).
In embodiments, the disease or disorder is a cancer selected from lung cancer, colon cancer, and oral squamous cancer. In embodiments, the cancer is oral squamous cancer. In embodiments, the subject in need of treatment is one diagnosed with a cancer, wherein the cancer cells carry at least one activating mutation in ALPK1, or wherein the cancer cells express ALPK1 mRNA or protein at elevated levels compared to non-cancer cells of the subject.
In embodiments, the disclosure further provides methods of identifying a disease, disorder, or condition for treatment with a compound of Formula I, or a subembodiment described herein, the methods comprising assaying a biological sample from a subject diagnosed with the disease, disorder, or condition for one or more of an activating mutation in A LPK1, and overexpression of A LPK1 mRNA or protein in cells or tissues involved in the disease, disorder, or condition, as compared to cells or tissues of a reference not involved in the disease, disorder, or condition. In embodiments, the activating mutation in ALPK1 is 2770T>C, p.(S924P).
In the context of the methods described here, the term “treating” may refer to the amelioration or stabilization of one or more symptoms associated with the disease, disorder or condition being treated. The term “treating” may also encompass the management of disease, disorder or condition, referring to the beneficial effects that a subject derives from a therapy but which does not result in a cure of the underlying disease, disorder, or condition.
In embodiments where a therapeutically effective amount of a compound described herein is administered to a subject, the therapeutically effective amount is the amount sufficient to achieve a desired therapeutic outcome, for example the amelioration or stabilization of one or more symptoms of the disease, disorder or condition being treated.
In embodiments, a therapeutically effective amount is the amount required to achieve at least an equivalent therapeutic effect compared to a standard therapy. An example of a standard therapy is an FDA-approved drug indicated for treating the same disease, disorder or condition.
In the context of any of the methods described here, the subject is preferably a human but may be a non-human mammal, preferably a non-human primate. In other embodiments, the non-human mammal may be, for example, a dog, cat, a rodent (e.g., a mouse, a rat, a rabbit), a horse, a cow, a sheep, a goat, or any other non-human mammal.
In embodiments, the human subject is selected from an adult human, a pediatric human, or a geriatric human, as those terms are understood by the medical practitioner, for example as defined by the U.S. Food and Drug Administration.
In embodiments, the disclosure provides pharmaceutical compositions comprising a compound of Formula I, or a subembodiment thereof, as described herein, and one or more carriers or excipients, preferably pharmaceutically acceptable carriers or excipients. As used herein, the phrase “pharmaceutically acceptable” refers to those compounds, materials, compositions, carriers, and/or dosage forms which are, within the scope of sound medical judgment, suitable for use in contact with the tissues of human beings and animals without excessive toxicity, irritation, allergic response, or other problem or complication, commensurate with a reasonable benefit/risk ratio. Excipients for preparing a pharmaceutical composition are generally those that are known to be safe and non-toxic when administered to a human or animal body. Examples of pharmaceutically acceptable excipients include, without limitation, sterile liquids, water, buffered saline, ethanol, polyol (for example, glycerol, propylene glycol, liquid polyethylene glycol and the like), oils, detergents, suspending agents, carbohydrates (e.g., glucose, lactose, sucrose or dextran), antioxidants (e.g., ascorbic acid or glutathione), chelating agents, low molecular weight proteins, and suitable mixtures of any of the foregoing. The particular excipients utilized in a composition will depend upon various factors, including chemical stability and solubility of the compound being formulated and the intended route of administration.
A pharmaceutical composition can be provided in bulk or unit dosage form. It is especially advantageous to formulate pharmaceutical compositions in unit dosage form for ease of administration and uniformity of dosage. The term “unit dosage form” refers to physically discrete units suited as unitary dosages for the subject to be treated; each unit containing a predetermined quantity of an active compound calculated to produce the desired therapeutic effect in association with the required pharmaceutical carrier. A unit dosage form can be an ampoule, a vial, a suppository, a dragee, a tablet, a capsule, an IV bag, or a single pump on an aerosol inhaler.
In therapeutic applications, dose may vary depending on the chemical and physical properties of the active compound as well as clinical characteristics of the subject, including e.g., age, weight, and co-morbidities. Generally, the dose should be a therapeutically effective amount. An effective amount of a pharmaceutical composition is that which provides an objectively identifiable improvement as noted by the clinician or other qualified observer. For example, alleviating a symptom of a disorder, disease or condition.
A pharmaceutical composition as described herein may take any suitable form (e.g. liquids, aerosols, solutions, inhalants, mists, sprays; or solids, powders, ointments, pastes, creams, lotions, gels, patches and the like) for administration by any desired route (e.g. pulmonary, inhalation, intranasal, oral, buccal, sublingual, parenteral, subcutaneous, intravenous, intramuscular, intraperitoneal, intrapleural, intrathecal, transdermal, transmucosal, rectal, and the like). In embodiments, the pharmaceutical composition is in the form of an orally acceptable dosage form including, but not limited to, capsules, tablets, buccal forms, troches, lozenges, and oral liquids in the form of emulsions, aqueous suspensions, dispersions or solutions. Capsules may contain excipients such as inert fillers and/or diluents including starches (e.g., corn, potato or tapioca starch), sugars, artificial sweetening agents, powdered celluloses, such as crystalline and microcrystalline celluloses, flours, gelatins, gums, etc. In the case of tablets for oral use, carriers which are commonly used include lactose and corn starch. Lubricating agents, such as magnesium stearate, can also be added.
In embodiments, the pharmaceutical composition is in the form of a tablet. The tablet can comprise a unit dose of a compound described here together with an inert diluent or carrier such as a sugar or sugar alcohol, for example lactose, sucrose, sorbitol or mannitol. The tablet can further comprise a non-sugar derived diluent such as sodium carbonate, calcium phosphate, calcium carbonate, or a cellulose or derivative thereof such as methyl cellulose, ethyl cellulose, hydroxypropyl methyl cellulose, and starches such as corn starch. The tablet can further comprise binding and granulating agents such as polyvinylpyrrolidone, disintegrants (e.g. swellable crosslinked polymers such as crosslinked carboxymethylcellulose), lubricating agents (e.g. stearates), preservatives (e.g. parabens), antioxidants (e.g. butylated hydroxytoluene), buffering agents (e.g. phosphate or citrate buffers), and effervescent agents such as citrate/bicarbonate mixtures. The tablet may be a coated tablet. The coating can be a protective film coating (e.g. a wax or varnish) or a coating designed to control the release of the active compound, for example a delayed release (release of the active after a predetermined lag time following ingestion) or release at a particular location in the gastrointestinal tract. The latter can be achieved, for example, using enteric film coatings such as those sold under the brand name Eudragit®.
Tablet formulations may be made by conventional compression, wet granulation or dry granulation methods and utilize pharmaceutically acceptable diluents, binding agents, lubricants, disintegrants, surface modifying agents (including surfactants), suspending or stabilizing agents, including, but not limited to, magnesium stearate, stearic acid, talc, sodium lauryl sulfate, microcrystalline cellulose, carboxymethylcellulose calcium, polyvinylpyrrolidone, gelatin, alginic acid, acacia gum, xanthan gum, sodium citrate, complex silicates, calcium carbonate, glycine, dextrin, sucrose, sorbitol, dicalcium phosphate, calcium sulfate, lactose, kaolin, mannitol, sodium chloride, talc, dry starches and powdered sugar. Preferred surface modifying agents include nonionic and anionic surface modifying agents. Representative examples of surface modifying agents include, but are not limited to, poloxamer 188, benzalkonium chloride, calcium stearate, cetostearyl alcohol, cetomacrogol emulsifying wax, sorbitan esters, colloidal silicon dioxide, phosphates, sodium dodecyl sulfate, magnesium aluminum silicate, and triethanolamine.
In embodiments, the pharmaceutical composition is in the form of a hard or soft gelatin capsule. In accordance with this formulation, the compound of the present invention may be in a solid, semi-solid, or liquid form.
In embodiments, the pharmaceutical composition is in the form of a sterile aqueous solution or dispersion suitable for parenteral administration. The term parenteral as used herein includes subcutaneous, intracutaneous, intravenous, intramuscular, intra-articular, intraarterial, intrasynovial, intrasternal, intrathecal, intralesional and intracranial injection or infusion techniques.
In embodiments, the pharmaceutical composition is in the form of a sterile aqueous solution or dispersion suitable for administration by either direct injection or by addition to sterile infusion fluids for intravenous infusion, and comprises a solvent or dispersion medium containing, water, ethanol, a polyol (e.g., glycerol, propylene glycol and liquid polyethylene glycol), suitable mixtures thereof, or one or more vegetable oils. Solutions or suspensions can be prepared in water with the aid of co-solvent or a surfactant. Examples of suitable surfactants include polyethylene glycol (PEG)-fatty acids and PEG-fatty acid mono and diesters, PEG glycerol esters, alcohol-oil transesterification products, polyglyceryl fatty acids, propylene glycol fatty acid esters, sterol and sterol derivatives, polyethylene glycol sorbitan fatty acid esters, polyethylene glycol alkyl ethers, sugar and its derivatives, polyethylene glycol alkyl phenols, polyoxyethylene-polyoxypropylene (POE-POP) block copolymers, sorbitan fatty acid esters, ionic surfactants, fat-soluble vitamins and their salts, water-soluble vitamins and their amphiphilic derivatives, amino acids and their salts, and organic acids and their esters and anhydrides. Dispersions can also be prepared, for example, in glycerol, liquid polyethylene glycols and mixtures of the same in oils.
The present disclosure also provides packaging and kits comprising pharmaceutical compositions for use in the methods described here. The kit can comprise one or more containers selected from the group consisting of a bottle, a vial, an ampoule, a blister pack, and a syringe. The kit can further include one or more of instructions for use, one or more syringes, one or more applicators, or a sterile solution suitable for reconstituting a compound or composition described here.
All percentages and ratios used herein, unless otherwise indicated, are by weight.
The invention is further described and exemplified by the following non-limiting examples.
In embodiments, a compound of Formula I, or a subembodiment described herein, is an inhibitor of ALPK1 as measured, for example, in an in vitro kinase assay, or an assay designed to measure the activation of downstream targets of ALPK1 pathway activation, for example NFkB transcriptional activation and the secretion of proinflammatory cytokines and chemokines, such as IL-8, which is also referred to as CXCL-8. In general, the computer program XL fit was used for data analysis, including non-linear regression analysis. The half maximal inhibitory concentration (IC50) was used as the measure of a compound's effectiveness in the assays. IC50 values were determined using the following logistic equation Y=min+(max−min)/(1+(X/IC50{circumflex over ( )}−hillslpoe), where Y is the value at the compound concentration, X. The concentration response curve fitting was conducted using GraphPad Prism version 6.00 software.
ALPK1 kinase activity was measured in an in vitro assay using ADP-Heptose as the ALPK1 ligand and activator of its kinase activity and TIFA protein as the ALPK1 phosphorylation substrate. Since phosphorylated TIFA proteins oligomerize, Homogeneous Time-Resolved Fluorescence (HTRF) was used to measure protein:protein interaction between HA-tagged TIFA proteins as an indicator of TIFA phosphorylation.
In brief, dose-response studies were performed with HEK293 cells cultured in Dulbecco's Modified Eagle Medium (DMEM) supplemented 10% fetal bovine serum (FBS, Hyclone™) containing antibiotics (pen/strep, G418) in 384-well assay plates. Each well contained 0.1 mg TIFA, ALPK1 (2 nM final concentration in reaction mixture) and kinase buffer (100 mM of HEPES pH 7.4, 4 mM DTT, 40 mM MgCl2, 20 mM of β-Glycerol phosphate disodium salt, 0.4 mM of Na3VO4, 0.16 mg/mL). Titrations of the test compounds were prepared in dimethylsulphoxide (DMSO). The reaction was initiated by addition of ATP and ADP-Heptose.
For HTRF, samples were incubated with a Tb cryptate-labeled anti-HA antibody for capturing HA-tagged proteins according to the manufacturer's instructions (PerkinElmer™, CisBio™) and the fluorescence signal was quantified (Tecan Infinite F NANO+). HTRF signals were calculated as the HTRF ratio (ratio of fluorescence measured at 665 nm and 620 nm)×104 (thereby using the signal at 620 nm as an internal standard).
All compounds exhibited a dose-dependent decrease in TIFA phosphorylation in this assay. IC50 values were determined using 3- or 4-parameter logistic equation using GraphPad Prism version 6.00. The reference compound, A027, was used as a positive control for each plate. This compound has an IC50 of ˜50 nanomolar (nM) in this assay. IC50 values for the test compounds ranged from 1 to 1000 nM and are shown in Tables 4-7.
An alkaline phosphatase reporter assay system was used to measure inhibition of ALPK1-dependent NFκB reporter gene activation. Briefly, HEK293 cells stably expressing an NF-kB reporter (referred to herein as “G9 cells”) were maintained in DMEM as described above. For the assay, cells were seeded into 96-well plates at a density of 10,000 cells/well in Freestyle™ 293 Expression Medium (ThermoFisher), and allowed to attach overnight. Cells were pretreated with serially diluted compounds for 30 min and then stimulated with D-glycero-D-manno-6-fluoro-heptose-1β-S-ADP. This compound is an analog of ADP-heptose that shows increased stability in vitro along with a similar ability to activate ALPK1 kinase activity. NFkB gene activation was detected using the chromogenic substrate, para-nitrophenyl phosphate (pNPP) according to the manufacturer's protocols (pNPP Phosphatase Assay, Beyotime Biotechnology). All compounds exhibited a dose-dependent decrease in NFkB promoter-driven gene expression in this assay. IC50 values ranged from 1-10 micromolar (uM) and are shown in Tables 4-7.
Activating mutations in ALPK1 are associated with diseases and disorders such as cancer, spiroandenoma, spiroandenocarcinoma, ROSAH syndrome, and PFAPA syndrome. We conducted further experiments to evaluate the ability of representative compounds to inhibit ALPK1 in the context of two activating mutations, T237M and VI092A. In preliminary experiments we determined that IL-8 protein secretion was elevated in cells transiently transfected with human ALPK1 expression vectors containing each of these activating mutations. Accordingly, we used IL-8 secretion as an indicator of activated ALPK1 inhibition in cells expressing these mutations.
First, in preliminary experiments, we established that IL-8 secretion was significantly increased in cells transiently expressing either of the two activating mutations, T237M or V1092A. HEK293 cells were cultured as described above prior to transient transfection with either empty vector or an expression vector encoding (i) human ALPK1 (hALPK1), (ii) hALPK1 with the T237M activating mutation (hALPK1-T237M) (iii) hALPK1 with the V1092A activating mutation (hALPK1-V1092A), or (iv) a kinase dead ALPK1 mutant (hALPK1-T237M-DI 194S). Transfection was performed according to manufacturer's protocols (Lipofectamine™ 3000, ThermoFisher). Transfected cells were selected, seeded onto 96-well plates and treated with serial dilutions of the test compounds for 6.5 hr. Following treatment, cell viability was determined using a luminescent cell viability assay (Cell Counting-Lite Assay or “CCL Assay” from Vazyme Biotech Co., Ltd.) and cell free supernatants were collected and analyzed for IL-8 protein by IL-8 ELISA as described above.
Next, we tested a representative set of compounds for inhibition of IL-8 secretion in cells expressing each of the activating ALPK1 mutants, T237M and V1092A. Table 8 shows inhibition of IL-8 secretion in cells transfected with the T237M and Table 9 shows inhibition of IL-8 secretion in cells transfected with the V1092A mutant. For the T237M mutant study, we produced an HEK293 cell line (“A2”) stably expressing the T237M hALPK1 mutant. A2 cells were cultured in the presence of test compound for 40 hours total. Fresh medium and compound were added at 24 hours. Cell viability and IL-8 secretion were determined 16 hours after the second addition of compound, using the CCL assay and IL-8 ELISA as described above. Table 8 shows half maximal inhibitory concentration (IC50) of IL-8 secretion in A2 cells, relative to IL-8 secretion from wild-type HEK293 cells, such that knockdown to the level of IL-8 from wild-type cells was considered to be 100% inhibition.
For the V1092A mutant study shown in Table 9, HEK293 cells were transiently transfected with hALPK1-V1092A or hALPK1 (wildtype) expression vectors and then treated with test compounds for 24 hours. Fresh medium and compound were added at 18 hours. Cell viability and IL-8 secretion were determined 6 hours after the second addition of compound, using the CCL assay and IL-8 ELISA as described above. Table 9 shows half maximal inhibitory concentration (IC50) of IL-8 secretion relative to wild-type HEK293 cells.
To test the effects of the ALPK1 inhibitors on the expression of innate immunity genes activated upon ALPK1 activation, SD rats were orally administered ALPK1 inhibitors followed by activation of innate immunity genes by intraperitoneal administration of an ALPK1 agonist, D-glycero-D-manno-6-fluoro-heptose-1β-S-ADP. Kidney tissue was harvested and assayed for gene expression. Briefly, Twenty male Sprague-Dawley (SD) rats were randomly divided into five groups. The normal group was given vehicle (0.5% MC) orally. After 2 hours, PBS was given by ip injection. The control group was given vehicle (0.5% MC) orally. After 2 hours, D-glycero-D-manno-6-fluoro-heptose-1β-S-ADP (50 μpk) was given by ip injection. The other 3 groups were given the ALPK1 inhibitor A0176 (4, 10 and 25 mpk) orally. After 2 hours, D-glycero-D-manno-6-fluoro-heptose-1β-S-ADP (50 μpk) was given by ip injection. The kidney from each group were collected after 3 hours of ip injection of D-glycero-D-manno-6-fluoro-heptose-1β-S-ADP (50 μpk). Samples were isolated for the RT-PCR to identify MCP-1 (CCL-2), CCL-7, CXCL-1, CXCL-10, IL-1p, IL-6 mRNA expression levels. Total RNA was extracted from kidney following the protocol of the Rneasy Mini Kit (QIAGEN, Germany). Messenger RNA was reverse transcribed to cDNA using HiScript Q RT SuperMix for qPCR Kit (Vazyme, Nanjing, China). Quantitative PCR was conducted using AceQ qPCR SYBR Green Master Mix Kit (Vazyme, Nanjing, China) on the QuantStudio 5 applied biosystems (Thermo scientific, USA). The relative mRNA levels were calculated using the 2-ΔΔCT method, and HPRT was used as a reference for gene expression normalization. Data were presented as the gene fold change. As shown in
Polymicrobial sepsis induced by cecal ligation and puncture (CLP) is the most frequently used model because it closely resembles the progression and characteristics of human sepsis. We used a rat CLP model to evaluate the effects of compounds described here on sepsis. Briefly, the rat cecum was ligated with sterile silk thread, and then cecum was punctured twice with a needle, gently squeezed to express a small amount of fecal material, then the abdominal incision was closed. Compounds C008 and A0176 (20 mg/kg) were dosed 2 hours prior to surgery, and survival was recorded over the next 24 hours. In addition, at 24 hours post-surgery, the kidneys were collected for gene expression analysis by Q-PCR and plasma was collected for measurement of plasma MCP-1 concentrations by ELISA. The results are shown in
Those skilled in the art will recognize or be able to ascertain using no more than routine experimentation, many equivalents to the specific embodiments of the invention as described herein. Such equivalents are intended to be encompassed by the following claims.
All references cited herein are incorporated herein by reference in their entirety and for all purposes to the same extent as if each individual publication or patent or patent application was specifically and individually indicated to be incorporated by reference in its entirety for all purposes.
The present invention is not to be limited in scope by the specific embodiments described herein. Indeed, various modifications of the invention in addition to those described herein will become apparent to those skilled in the art from the foregoing description and accompanying figures. Such modifications are intended to fall within the scope of the appended claims.
| Number | Date | Country | Kind |
|---|---|---|---|
| PCT/CN2020/117436 | Sep 2020 | WO | international |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/CN2021/119801 | 9/23/2021 | WO |
