Patent Grant
11613533
The Rearranged during transfection (RET) kinase is a single-pass transmembrane receptor belonging to the tyrosine kinase superfamily that is required for normal development, maturation, and maintenance of several tissues and cell types. The extracellular portion of the RET kinase contains four calcium-dependent cadherin-like repeats involved in ligand binding and a juxtamembrane cysteine-rich region necessary for the correct folding of the RET extracellular domain, while the cytoplasmic portion of the receptor includes two tyrosine kinase subdomains.
RET signaling is mediated by the binding of a group of 35 soluble proteins of the glial cell line-derived neurotrophic factor (GDNF) family ligands (GFLs), which also includes neurturin (NTRN), artemin (ARTN), and persephin (PSPN). Unlike other receptor tyrosine kinases, RET does not directly bind to GFLs and requires an additional co-receptor, which can be one of four GDNF family receptor-α(GFRα) family members that are tethered to the cell surface by a glycosylphosphatidylinositol linkage. GFLs and GFRα family members form binary complexes that in turn bind to RET and recruit it into cholesterol-rich membrane subdomains where RET signaling occurs.
Upon binding of the ligand-co-receptor complex, RET dimerization and autophosphorylation on intracellular tyrosine residues recruits adaptor and signaling proteins to stimulate multiple downstream pathways. Adaptor protein binding to these docking sites leads to activation of Ras-MAPK and PI3K-Akt/mTOR signaling pathways or to recruitment of the CBL family of ubiquitin ligases that functions in RET downregulation of the RET-mediated functions.
Disruptions in normal RET activity due to abnormal RET expression stemming from genetic alterations in the RET kinase, including protein-gene fusions and activating point mutations, lead to overactive RET signaling and uncontrolled cell growth, e.g., various cancer types and certain gastrointestinal disorders such as irritable bowel syndrome (IBS). The ability to inhibit abnormal RET activity in patients with cancer or other disorders related to overactive RET signaling would be of great benefit to those patients. Additionally, some RET kinase genetic alterations are altering the conformational structure of a RET kinase to such an extent that a given RET kinase inhibitor may be less effective (or ineffective). In such cases, new RET kinase inhibitors that are effective to the modified RET kinase would greatly benefit patients.
Compounds of the formula:
pharmaceutically acceptable salts thereof, and pharmaceutical compositions thereof, are provided herein. In formula (I), A can be a five- or six-member aryl or heteroaryl; R1 can be hydrogen, halogen, C1-C6 alkyl, C1-C6 heteroalkyl, —(C0-C4 alkyl)(C5-C6 heteroalkyl), —(C0-C4 alkyl)(C3-C7 cycloalkyl), —(C0-C4 heteroalkyl)(C3-C7 cycloalkyl), —(C0-C4 alkyl)(C4-C7 cycloheteroalkyl), —(C0-C4 heteroalkyl)(C3-C7 cycloheteroalkyl), —(C0-C4 alkyl)(C4-C10 bicyclic), —(C0-C4 alkyl)(C5-C6 aryl), —(C0-C4 alkyl)(C5-C6 heteroaryl), —(C0-C4 alkyl)(C4-C10 heterobicyclic), C5-C12 spirane, C5-C12 heterospirane, adamantane, difluoromethylsulfane, or pentafluorosulfane, wherein each R1 is optionally substituted with one or more groups that are independently halogen, cyano, hydroxyl, oxo, methyl, methoxy, hydroxymethyl, ethyl, ethoxy, hydroxyethyl, methylamine, N,N-diethylmethylamine, or mono-, di-, or tri-halomethyl, and wherein two R1 groups can fuse to form a ring structure that includes a portion of A and is optionally aromatic, and n is 1, 2, 3, 4 or 5; X1, X2, X3, and X4 each can be independently N, CH, C—CH3, C—CH2—OH, C—OCH3, C—CH2—OCH3 or C-halogen; and R2 can be C1-C4 alkyl, —(C0-C4 alkyl)(C3-C7 cycloalkyl), —(C0-C4 alkyl)(C4-C7 heterocycloalkyl), —(C0-C4 alkyl)(C4-C10 bicyclic), with each being optionally substituted with one or more groups that are independently deuterium, halogen, cyano, hydroxyl, oxo, methyl, methoxy, hydroxymethyl, ethyl, ethoxy, hydroxyethyl, cyclopropyl, or mono-, di-, or tri-halomethyl. The compounds of formula (I) contain a chiral center providing an R-enantiomeric form and an S-enantiomeric form as shown here:
The R-enantiomer and S-enantiomer, pharmaceutically acceptable salts thereof, and pharmaceutical compositions thereof, in which A, R1, n, X1, X2, X3, X4, and R2 are defined herein are also provided. It is understood that formulas II and III are subspecies of formula I, and thus, references to formula I throughout this application also apply to formulas II and III.
Methods of using the compounds of formulas I, II, or III, pharmaceutically acceptable salts thereof, and pharmaceutical compositions thereof, to treat cancer, in particular for the treatment of cancer with abnormal RET expression (e.g., a RET-associated cancer like medullary thyroid cancer or RET fusion lung cancer) are also provided. The methods include administering a therapeutically effective amount of a compound of formulas I, II, or III, or a pharmaceutically acceptable salt thereof, to a patient in need.
Also provided herein, are compounds of formulas I, II, and III, and pharmaceutically acceptable salts thereof, for use in therapy. Further provided herein, are the compounds of formulas I, II, and III, and pharmaceutically acceptable salts thereof, for use in the treatment of cancer, in particular for use in the treatment of cancer with abnormal RET expression (e.g., a RET-associated cancer like medullary thyroid cancer or RET fusion lung cancer). The use of compounds of formulas I, II, and III, or pharmaceutically acceptable salts thereof, in the manufacture of a medicament for treating cancer, in particular for use in the treatment of cancer with abnormal RET expression (e.g., a RET-associated cancer like medullary thyroid cancer or RET fusion lung cancer), is also provided.
Novel RET kinase inhibitor compounds are described herein. These new compounds could address the need for potent, effective treatment of disorders associated with abnormal RET activity, e.g., IBS or cancer, especially cancer stemming from overactive RET signaling (i.e., RET-associated cancers). More specifically, these new compounds could address the need for potent, effective treatment of RET-associated cancers such as lung cancer (e.g., small cell lung carcinoma or non-small cell lung carcinoma), thyroid cancer (e.g., papillary thyroid cancer, medullary thyroid cancer, differentiated thyroid cancer, recurrent thyroid cancer, or refractory differentiated thyroid cancer), thyroid adenoma, endocrine gland neoplasms, lung adenocarcinoma, bronchioles lung cell carcinoma, multiple endocrine neoplasia type 2A or 2B (MEN2A or MEN2B, respectively), pheochromocytoma, parathyroid hyperplasia, breast cancer, mammary cancer, mammary carcinoma, mammary neoplasm, colorectal cancer (e.g., metastatic colorectal cancer), papillary renal cell carcinoma, ganglioneuromatosis of the gastroenteric mucosa, inflammatory myofibroblastic tumor, or cervical cancer.
The compounds described herein are compounds of formula (I):
or pharmaceutically acceptable salts thereof. In formula (I),
A is a five- or six-member aryl or heteroaryl;
Each R1 can be attached to A at various chemically appropriate positions and is independently hydrogen, halogen, C1-C6 alkyl, C1-C6 heteroalkyl, —(C0-C4 alkyl)(C5-C6 heteroalkyl), —(C0-C4 alkyl)(C3-C7 cycloalkyl), —(C0-C4 heteroalkyl)(C3-C7 cycloalkyl), —(C0-C4 alkyl)(C4-C7 cycloheteroalkyl), —(C0-C4 heteroalkyl)(C3-C7 cycloheteroalkyl), —(C0-C4 alkyl)(C4-C10 bicyclic), —(C0-C4 alkyl)(C5-C6 aryl), —(C0-C4 alkyl)(C5-C6 heteroaryl), —(C0-C4 alkyl)(C4-C10 heterobicyclic), C5-C12 spirane, C5-C12 heterospirane, adamantane, difluoromethylsulfane, or pentafluorosulfane, wherein each R1 is optionally substituted with one or more groups that are independently halogen, cyano, hydroxyl, oxo, methyl, methoxy, hydroxymethyl, ethyl, ethoxy, hydroxy ethyl, methylamine, N,N-diethylmethylamine, or mono-, di-, or tri-halomethyl, and wherein two R1 groups can fuse to form a ring structure that includes a portion of A and is optionally aromatic, and n is 1, 2, 3, 4, or 5;
X1, X2, X3, and X4 are each independently N, CH, C—CH3, C—CH2—OH, C—OCH3, C—CH2—OCH3 or C-halogen; and
R2 is C1-C4 alkyl, —(C0-C4 alkyl)(C3-C7 cycloalkyl), —(C0-C4 alkyl)(C4-C7 heterocycloalkyl), —(C0-C4 alkyl)(C4-C10 bicyclic) each optionally substituted with one or more groups that are independently deuterium, halogen, cyano, hydroxyl, oxo, methyl, methoxy, hydroxymethyl, ethyl, ethoxy, hydroxyethyl, cyclopropyl, or mono-, di-, or tri-halomethyl.
While n is defined as 1, 2, 3, 4, or 5, some A-rings have 5 positions that may accommodate an R1 group, while others do not. For example, phenyl has 5 substitutable positions, pyrazoles have three substitutable positions, while an isoxazole has only two. Thus, the maximum value of the variable n can depend on the identity of the A-ring.
The specific chemical naming conventions used herein are intended to be familiar to one of skill in the chemical arts. Some terms are defined specifically for additional clarity.
As used herein, the term alkyl means saturated linear or branched-chain monovalent hydrocarbon radicals of one to four atoms, e.g., “C1-C4 alkyl.” In cases where a zero is indicated, e.g., C0-C4 alkyl, this component of the substituent group can be absent, thus, if a C5 heterocycloalkyl substituent is at the R2 position in formula (I), the C5 heterocycloalkyl substituent would be described by the —(C0-C4 alkyl)(C4-C7 heterocycloalkyl) substituent as described for R2 (i.e., the substituent group would be —(C0)(C5 heterocycloalkyl). Examples include, but are not limited to, methyl, ethyl, propyl, 1-propyl, isopropyl, and butyl. Similarly, as used herein, the term heteroalkyl means saturated linear or branched-chain monovalent alkyl molecules as defined herein containing one or more heteroatoms that have replaced carbon(s) in the alkyl chain.
As used herein, the term C5-C6 aryl refers to a functional group or substituent derived from an aromatic ring containing five to seven carbon atoms and no heteroatoms. As used herein, the term C5-C6 heteroaryl refers to a functional group or substituent derived from an aromatic ring containing carbon atoms and one or more heteroatoms (e.g., nitrogen, oxygen, or sulphur) as part of the aromatic ring such that that ring contains from five to seven atoms. Examples of aryl and heteroaryl groups include, but are not limited to, benzene, pyridine, pyrazine, pyrimidine, pyridazine, furan, pyrrole, thiophene, imidazole, pyrazole, oxazole, isoxazole, and thiazole.
As used herein, the term C3-C7 cycloalkyl means a cyclic alkyl molecule containing three to seven carbon atoms. Examples of C3-C7 cycloalkyls include, but are not limited to, cyclopropyl, cyclobutyl, and cyclopentyl. Similarly, as used herein, the term C4-C7 cycloheteroalkyl means a cycloalkyl molecule as defined herein, containing four to seven total atoms and including one or more hetero atoms that have replaced carbon(s) in the cycloalkyl chain.
As used herein, the term C4-C10 bicyclic refers to a group having two or more fused or bridged rings made from four to ten carbon atoms. When the C4-C10 bicyclic group is fused, the two rings share two adjacent atoms. When the C4-C10 bicyclic group is bridged, the two rings share three or more atoms. Bicyclic molecules can be all aliphatic, all aromatic, or mixed aromatic and aliphatic. The term C4-C10 heterobicyclic refers to C4-C10 bicyclic groups as defined that also include one or more hetero atoms. Examples of bridged C4-C8 bicycloalkyl molecules useful with the compounds of formula (I) include, but are not limited to:
As used herein, the term C5-C12 spirane refers to a group having two or more rings made from seven to twelve carbon atoms connected through a single common carbon atom. Similarly, the term C5-C12 heterospirane refers to a group having two or more rings made from seven to twelve atoms including carbon and at least one hetero atom joined by a spirocyclic linkage through a carbon atom, wherein each ring has three to six ring atoms (with one carbon atom being common to both rings), and wherein two of the ring atoms are nitrogen atoms. Examples of C5-C12 spiranes and heterospiranes useful with the compounds of formula (I) include, but are not limited to:
As used herein, the term halogen means fluoro (F), chloro (Cl), bromo (Br), or iodo (I).
As used herein, the term oxo means an oxygen that is double-bonded to a carbon atom.
In the compounds of formula (I), A-(R1)n can be
wherein a wavy line indicates the connection point of A to the backbone as shown in formula (I).
In one embodiment, in the compounds of formula (I), A-(R1)n is
In an embodiment, in the compounds of formula (I), A-(R1)n is
In another embodiment, in the compounds of formula (I), A-(R1)n is
In a preferred embodiment, the halogen is F or Cl.
In yet another embodiment, in the compounds of formula (I), A-(R1)n is
In another embodiment, in the compounds of formula (I), A-(R1)n can be
In an embodiment, in the compounds of formula (I), A-(R1)n is
and n is 1.
In a further embodiment, in the compounds of formula (I), A-(R1)n is
In an embodiment, A-(R1)n is a phenyl substituted with (R1)n. In a further embodiment, n is 1-4, or 1-3, or 1-2, or 1, or 2, or 2-4, or 2-5. In some embodiments when A-(R1)n is a phenyl substituted with (R1)n, two R1 groups fuse to form a ring structure that includes a portion of A and is optionally aromatic, the resulting A-ring is optionally substituted, as described herein.
In some embodiments, in the compounds of formula (I), each R1 is independently selected from the group consisting of H, —CH3, —CH2C(CH3)3, —C(CH3)2CF3,
In further embodiments, in the compounds of formula (I), at least one R1 group is H or CH3.
In another embodiment, in the compounds of formula (I), at least one R1 is halogen,
—CH2C(CH3)3, 2-chloro-4-fluorophenyl, 2,4-dichlorophenyl, —CH2C(CH3)3, —C(CH3)2CF3,
—C(CH3)2CH2CH3, —C(CH3)2CF2CH3, —C(CH3)2CH2CF3, —C(CH3)3,
or CF3.
In yet another embodiment, at least one R1 is halogen, —CH2C(CH3)3,
In still yet another embodiment, at least one R1 is CH3, —CH2C(CH3)3, —C(CH3)2CF3, C(CH3)2CH2CH3, —C(CH3)2CF2CH3, —C(CH3)2CH2CF3, —C(CH3)3, or CF3.
In another embodiment, at least one R1 is an optionally substituted C5-C12 spirane.
In still another embodiment, at least one R1 is difluoromethylsulfane, or pentafluorosulfane.
In yet still another embodiment, at least one R1 is 2-fluoro-4-chlorophenyl; 2-chloro-4-fluorophenyl; 2,4-dichlorophenyl; or 2,4-difluorophenyl.
In the compounds of formula (I), R2 can be
where the wavy line indicates connection the backbone.
In some embodiments, in the compounds of formula (I), R2 is —CH(CH3)2, —CH(CF3)CH3, —CH(CH3)CHF2, or
In other embodiments, in the compounds of formula (I), R2 is
In another embodiment, in the compounds of formula (I), R2 is
In still another embodiment, in the compounds of formula (I), R2 is
In some embodiments, in the compounds of formula (I), R2 is deuterated, i.e., it contains at least one deuterium. In some further embodiments, deuterated R2 is —CH(CH3)CF2D, —CH(CD3)2, —CH(CF3)CD3, —CH(CH3)CDF2, —CD(CD3)2, or —CD(CH3)CD3.
In some embodiments, R2 is —CH(CD3)2.
In various embodiments, X1, X2, X3, and X4 are CH.
In other embodiments, X1, X2, X3, and X4 are each independently CH, C—CH3, C—CH2—OH, C—OCH3, C—CH2—OCH3 or C-halogen, wherein at least one of X1, X2, X3, and X4 is not CH.
In some embodiments, two of X1, X2, X3, and X4 are CH, while the other two are C-halogen. In a further embodiment, X1 and X2 are CF, and X3 and X4 are CH.
In various embodiments, three of X1, X2, X3, and X4 are CH, while one is C-halogen. In a further embodiment, X2 is CF, while X1, X3 and X4 are CH.
In still other embodiments, one of X1, X2, X3, and X4 is N.
In a further embodiment, X2 is N and at least two of X1, X3, and X4 is CH.
In a still further embodiment, X1 is N and at least two of X2, X3, and X4 is CH.
In all of the above embodiments, it is understood that the definitions of variables apply to the non-salt forms “or a pharmaceutically acceptable salt thereof.”
One of skill in the art will appreciate that compounds as described by formula (I), or pharmaceutically acceptable salts thereof, contain at least one chiral center, the position of which is indicated by an ϕ in formula (I)ϕ:
(other chiral centers may also be created by various optional substitution patterns of Ru and R2 and can create further diastereomer sets). One of skill in the art will also appreciate that the Cahn-Ingold-Prelog (R) or (S) designations for chiral centers will vary depending upon the substitution patterns around a chiral center. The chiral center noted in the compound of formula (I) provides an R-enantiomeric form shown by formula (II) and an S-enantiomeric from shown by formula (III):
Compounds of formula (II) and formula (III) or pharmaceutically acceptable salts thereof, in which A, R1, n, X1, X2, X3, X4, and R2 are defined as for formula (I), are also provided herein. If multiple chiral centers are present, then diastereomers may also be present.
In one aspect, in the compounds of formulas (I), (II) and/or (III), R2 is isopropyl; X1, X2, X3, and X4 are CH; A-(R1)n is
where R1 is selected from the group consisting of H, —CH3, —CH2C(CH3)3, —C(CH3)2CF3,
In another aspect, in the compounds of formulas (I), (II) and/or (III), R2 is isopropyl; three of X1, X2, X3, and X4 are CH, while one of X1, X2, X3, and X4 is N; A-(R1)n is
where R1 is selected from the group consisting of H, —CH3, —CH2C(CH3)3, —C(CH3)2CF3,
In an aspect, in the compounds of formulas (I), (II) and/or (III), R2 is
X1, X2, X3, and X4 are CH; A-(R1)n is
where R1 is selected from the group consisting of H, —CH3, —CH2C(CH3)3, —C(CH3)2CF3,
In a further aspect, in the compounds of formulas (I), (II) and/or (III), R2 is
three of X1, X2, X3, and X4 are CH, while one of X1, X2, X3, and X4 is N; A-(R1)n is
where R1 is selected from the group consisting of H, —CH3, —CH2C(CH3)3, —C(CH3)2CF3,
In a further aspect, in the compounds of formulas (I), (II) and/or (III), R2 is —CH(CH3)CF2D, —CH(CD3)2, —CH(CF3)CD3, —CH(CH3)CDF2, —CD(CD3)2, or —CD(CH3)CD3; X1, X2, X3, and X4 are CH; A-(R1)n is
where R1 is selected from the group consisting of H, —CH3, —CH2C(CH3)3, —C(CH3)2CF3,
In a yet still further aspect, in the compounds of formulas (I), (II) and/or (III), R2 is —CH(CH3)CF2D, —CH(CD3)2, —CH(CF3)CD3, —CH(CH3)CDF2, —CD(CD3)2, or —CD(CH3)CD3; three of X1, X2, X3, and X4 are CH, while one of X1, X2, X3, and X4 is N; A-(R1)n is
where R1 is selected from the group consisting of H, —CH3, —CH2C(CH3)3, —C(CH3)2CF3,
In one aspect, in the compounds of formulas (I), (II) and/or (III), R2 is isopropyl; X1, X2, X3, and X4 are CH; A-(R1)n is
where R1 is selected from the group consisting of H, —CH3, —CH2C(CH3)3, —C(CH3)2CF3,
In another aspect, in the compounds of formulas (I), (II) and/or (III), R2 is isopropyl; three of X1, X2, X3, and X4 are CH, while one of X1, X2, X3, and X4 is N; A-(R1)n is
where R1 is selected from the group consisting of H, —CH3, —CH2C(CH3)3, —C(CH3)2CF3,
In an aspect, in the compounds of formulas (I), (II) and/or (III), R2 is
X1, X2, X3, and X4 are CH; A-(R1)n is
where R1 is selected from the group consisting of H, —CH3, —CH2C(CH3)3, —C(CH3)2CF3,
In a further aspect, in the compounds of formulas (I), (II) and/or (III), R2 is
three of X1, X2, X3, and X4 are CH, while one of X1, X2, X3, and X4 is N; A-(R1)n is
where R1 is selected from the group consisting of H, —CH3, —CH2C(CH3)3, —C(CH3)2CF3,
In a further aspect, in the compounds of formulas (I), (II) and/or (III), R2 is —CH(CH3)CF2D, —CH(CD3)2, —CH(CF3)CD3, —CH(CH3)CDF2, —CD(CD3)2, or —CD(CH3)CD3; X1, X2, X3, and X4 are CH; A-(R1)n is
where R1 is selected from the group consisting of H, —CH3, —CH2C(CH3)3, —C(CH3)2CF3,
In a yet still further aspect, in the compounds of formulas (I), (II) and/or (III), R2 is —CH(CH3)CF2D, —CH(CD3)2, —CH(CF3)CD3, —CH(CH3)CDF2, —CD(CD3)2, or —CD(CH3)CD3; three of X1, X2, X3, and X4 are CH, while one of X1, X2, X3, and X4 is N; A-(R1)n is
where R1 is selected from the group consisting of H, —CH3, —CH2C(CH3)3, —C(CH3)2CF3,
In another aspect, in the compounds of formulas (I), (II) and/or (III), R2 is isopropyl; X1, X2, X3, and X4 are CH; A-(R1)n is
where each R1 is selected from the group consisting of H, —CH3, —CH2C(CH3)3, —C(CH3)2CF3,
In an aspect, in the compounds of formulas (I), (II) and/or (III), R2 is isopropyl; three of X1, X2, X3, and X4 are CH, while one of X1, X2, X3, and X4 is N; A-(R1)n is
where each R1 is selected from the group consisting of H, —CH3, —CH2C(CH3)3, —C(CH3)2CF3,
In an aspect, in the compounds of formulas (I), (II) and/or (III), R2 is
X1, X2, X3, and X4 are CH; A-(R1)n is
where each R1 is selected from the group consisting of H, —CH3, —CH2C(CH3)3, —C(CH3)2CF3,
In a further aspect, in the compounds of formulas (I), (II) and/or (III), R2 is
three of X1, X2, X3, and X4 are CH, while one of X1, X2, X3, and X4 is N; A-(R1)n is
where each R1 is selected from the group consisting of H, —CH3, —CH2C(CH3)3, —C(CH3)2CF3,
In a further aspect, in the compounds of formulas (I), (II) and/or (III), R2 is —CH(CH3)CF2D, —CH(CD3)2, —CH(CF3)CD3, —CH(CH3)CDF2, —CD(CD3)2, or —CD(CH3)CD3; X1, X2, X3, and X4 are CH; A-(R1)n is
where each R1 is selected from the group consisting of H, —CH3, —CH2C(CH3)3, —C(CH3)2CF3,
In a yet still further aspect, in the compounds of formulas (I), (II) and/or (III), R2 is —CH(CH3)CF2D, —CH(CD3)2, —CH(CF3)CD3, —CH(CH3)CDF2, —CD(CD3)2, or —CD(CH3)CD3; three of X1, X2, X3, and X4 are CH, while one of X1, X2, X3, and X4 is N; A-(R1)n is
where each R1 is selected from the group consisting of H, —CH3, —CH2C(CH3)3, —C(CH3)2CF3
In one aspect, in the compounds of formulas (I), (II) and/or (III), R2 is isopropyl; X1, X2, X3, and X4 are CH; A-(R1)n is
where each R1 is selected from the group consisting of H, —CH3, —CH2C(CH3)3, —C(CH3)2CF3,
In another aspect, in the compounds of formulas (I), (II) and/or (III), R2 is isopropyl; three of X1, X2, X3, and X4 are CH, while one of X1, X2, X3, and X4 is N; A-(R1)n is
where each R1 is selected from the group consisting of H, —CH3, —CH2C(CH3)3, —C(CH3)2CF3,
In an aspect, in the compounds of formulas (I), (II) and/or (III), R2 is
X1, X2, X3, and X4 are CH; A-(R1)n is
where each R1 is selected from the group consisting of H, —CH3, —CH2C(CH3)3, —C(CH3)2CF3,
In a further aspect, in the compounds of formulas (I), (II) and/or (III), R2 is
three of X1, X2, X3, and X4 are CH, while one of X1, X2, X3, and X4 is N; A-(R1)n is
where each R1 is selected from the group consisting of H, —CH3, —CH2C(CH3)3, —C(CH3)2CF3,
In a further aspect, in the compounds of formulas (I), (II) and/or (III), R2 is —CH(CH3)CF2D, —CH(CD3)2, —CH(CF3)CD3, —CH(CH3)CDF2, —CD(CD3)2, or —CD(CH3)CD3; X1, X2, X3, and X4 are CH; A-(R1)n is
where each R1 is selected from the group consisting of H, —CH3, —CH2C(CH3)3, —C(CH3)2CF3,
In a yet still further aspect, in the compounds of formulas (I), (II) and/or (III), R2 is —CH(CH3)CF2D, —CH(CD3)2, —CH(CF3)CD3, —CH(CH3)CDF2, —CD(CD3)2, or —CD(CH3)CD3; three of X1, X2, X3, and X4 are CH, while one of X1, X2, X3, and X4 is N; A-(R1)n is
where each R1 is selected from the group consisting of H, —CH3, —CH2C(CH3)3, —C(CH3)2CF3,
In one aspect, in the compounds of formulas (I), (II) and/or (III), R2 is isopropyl; X1, X2, X3, and X4 are CH; A-(R1)n is
where R1 is selected from the group consisting of H, —CH3, —CH2C(CH3)3, —C(CH3)2CF3,
In another aspect, in the compounds of formulas (I), (II) and/or (III), R2 is isopropyl; three of X1, X2, X3, and X4 are CH, while one of X1, X2, X3, and X4 is N; A-(R1)n
where R1 is selected from the group consisting of H, —CH3, —CH2C(CH3)3, —C(CH3)2CF3,
In an aspect, in the compounds of formulas (I), (II) and/or (III), R2 is
X1, X2, X3, and X4 are CH; A-(R1)n is
where R1 is selected from the group consisting of H, —CH3, —CH2C(CH3)3, —C(CH3)2CF3,
In a further aspect, in the compounds of formulas (I), (II) and/or (III), R2 is
three of X1, X2, X3, and X4 are CH, while one of X1, X2, X3, and X4 is N; A-(R1)n is
where R1 is selected from the group consisting of H, —CH3, —CH2C(CH3)3, —C(CH3)2CF3,
In a further aspect, in the compounds of formulas (I), (II) and/or (III), R2 is —CH(CH3)CF2D, —CH(CD3)2, —CH(CF3)CD3, —CH(CH3)CDF2, —CD(CD3)2, or —CD(CH3)CD3; X1, X2, X3, and X4 are CH; A-(R1)n is
where R1 is selected from the group consisting of H, —CH3, —CH2C(CH3)3, —C(CH3)2CF3,
In a yet still further aspect, in the compounds of formulas (I), (II) and/or (III), R2 is —CH(CH3)CF2D, —CH(CD3)2, —CH(CF3)CD3, —CH(CH3)CDF2, —CD(CD3)2, or —CD(CH3)CD3; three of X1, X2, X3, and X4 are CH, while one of X1, X2, X3, and X4 is N; A-(R1)n is
where R1 is selected from the group consisting of H, —CH3, —CH2C(CH3)3, —C(CH3)2CF3,
In one aspect, in the compounds of formulas (I), (II) and/or (III), R2 is isopropyl; X1, X2, X3, and X4 are CH; A-(R1)n is
where each R1 is selected from the group consisting of H, —CH3, —CH2C(CH3)3, —C(CH3)2CF3,
In another aspect, in the compounds of formulas (I), (II) and/or (III), R2 is isopropyl; three of X1, X2, X3, and X4 are CH, while one of X1, X2, X3, and X4 is N; A-(R1)n is
where each R1 is selected from the group consisting of H, —CH3, —CH2C(CH3)3, —C(CH3)2CF3,
In an aspect, in the compounds of formulas (I), (II) and/or (III), R2 is
X1, X2, X3, and X4 are CH; A-(R1)n is
where each R1 is selected from the group consisting of H, —CH3, —CH2C(CH3)3, —C(CH3)2CF3,
In a further aspect, in the compounds of formulas (I), (II) and/or (III), R2 is
three of X1, X2, X3, and X4 are CH, while one of X1, X2, X3, and X4 is N; A-(R1)n is
where each R1 is selected from the group consisting of H, —CH3, —CH2C(CH3)3, —C(CH3)2CF3,
In a further aspect, in the compounds of formulas (I), (II) and/or (III), R2 is —CH(CH3)CF2D, —CH(CD3)2, —CH(CF3)CD3, —CH(CH3)CDF2, —CD(CD3)2, or —CD(CH3)CD3; X1, X2, X3, and X4 are CH; A-(R1)n is
where each R1 is selected from the group consisting of H, —CH3, —CH2C(CH3)3, —C(CH3)2CF3,
In a yet still further aspect, in the compounds of formulas (I), (II) and/or (III), R2 is —CH(CH3)CF2D, —CH(CD3)2, —CH(CF3)CD3, —CH(CH3)CDF2, —CD(CD3)2, or —CD(CH3)CD3; three of X1, X2, X3, and X4 are CH, while one of X1, X2, X3, and X4 is N; A-(R1)n is
where each R1 is selected from the group consisting of H, —CH3, —CH2C(CH3)3, —C(CH3)2CF3,
In another aspect, in the compounds of formulas (I), (II) and/or (III), R2 is isopropyl; X1, X2, X3, and X4 are CH; A-(R1)n is
where R1 is halogen,
—CH2C(CH3)3, 2-chloro-4-fluorophenyl, 2,4-dichlorophenyl, —CH2C(CH3)3, —C(CH3)2CF3,
—C(CH3)2CH2CH3, —C(CH3)2CF2CH3, —C(CH3)2CH2CF3, —C(CH3)3,
or CF3.
In an aspect, in the compounds of formulas (I), (II) and/or (III), R2 is isopropyl; three of X1, X2, X3, and X4 are CH, while one of X1, X2, X3, and X4 is N; A-(R1)n is
where R1 is halogen,
—CH2C(CH3)3, 2-chloro-4-fluorophenyl, 2,4-dichlorophenyl, —CH2C(CH3)3, —C(CH3)2CF3
—C(CH3)2CH2CH3, —C(CH3)2CF2CH3, —C(CH3)2CH2CF3, —C(CH3)3,
or CF3.
In an aspect, in the compounds of formulas (I), (II) and/or (III), R2 is
X1, X2, X3, and X4 are CH; A-(R1)n is
where R1 is halogen,
CH2C(CH3)3, 2-chloro-4-fluorophenyl, 2,4-dichlorophenyl, —CH2C(CH3)3, —C(CH3)2CF3,
C(CH3)2CH2CH3, —C(CH3)2CF2CH3, C(CH3)2CH2CF3, —C(CH3)3,
or CF3.
In a further aspect, in the compounds of formulas (I), (II) and/or (III), R2 is
three of X1, X2, X3, and X4 are CH, while one of X1, X2, X3, and X4 is N; A-(R1)n is
where R1 is halogen,
—CH2C(CH3)3, 2-chloro-4-fluorophenyl, 2,4-dichlorophenyl, —CH2C(CH3)3, —C(CH3)2CF3,
—C(CH3)2CH2CH3, —C(CH3)2CF2CH3, —C(CH3)2CH2CF3, —C(CH3)3,
or CF3.
In a further aspect, in the compounds of formulas (I), (II) and/or (III), R2 is —CH(CH3)CF2D, —CH(CD3)2, —CH(CF3)CD3, —CH(CH3)CDF2, —CD(CD3)2, or —CD(CH3)CD3; X1, X2, X3, and X4 are CH; A-(R1)n is
where R1 is halogen,
—CH2C(CH3)3, 2-chloro-4-fluorophenyl, 2,4-dichlorophenyl, —CH2C(CH3)3, —C(CH3)2CF3,
—C(CH3)2CH2CH3, —C(CH3)2CF2CH3, —C(CH3)2CH2CF3, —C(CH3)3,
or CF3.
In a yet still further aspect, in the compounds of formulas (I), (II) and/or (III), R2 is —CH(CH3)CF2D, —CH(CD3)2, —CH(CF3)CD3, —CH(CH3)CDF2, —CD(CD3)2, or —CD(CH3)CD3; three of X1, X2, X3, and X4 are CH, while one of X1, X2, X3, and X4 is N; A-(R1)n is
where R1 is halogen,
—CH2C(CH3)3, 2-chloro-4-fluorophenyl, 2,4-dichlorophenyl, —CH2C(CH3)3, —C(CH3)2CF3,
—C(CH3)2CH2CH3, —C(CH3)2CF2CH3, —C(CH3)2CH2CF3, —C(CH3)3,
or CF3.
In another aspect, in the compounds of formulas (I), (II) and/or (III), R2 is isopropyl; X1, X2, X3, and X4 are CH; A-(R1)n is
where R1 is halogen,
—CH2C(CH3)3, 2-chloro-4-fluorophenyl, 2,4-dichlorophenyl, —CH2C(CH3)3, —C(CH3)2CF3,
—C(CH3)2CH2CH3, —C(CH3)2CF2CH3, —C(CH3)2CH2CF3, —C(CH3)3,
or CF3.
In an aspect, in the compounds of formulas (I), (II) and/or (III), R2 is isopropyl; three of X1, X2, X3, and X4 are CH, while one of X1, X2, X3, and X4 is N; A-(R1)n is
where R1 is halogen is halogen,
—CH2C(CH3)3, 2-chloro-4-fluorophenyl, 2,4-dichlorophenyl, —CH2C(CH3)3, —C(CH3)2CF3,
—C(CH3)2CH2CH3, —C(CH3)2CF2CH3, —C(CH3)2CH2CF3, —C(CH3)3,
or CF3.
In an aspect, in the compounds of formulas (I), (II) and/or (III), R2 is
X1, X2, X3, and X4 are CH; A-(R1)n is
where R1 is halogen,
CH2C(CH3)3, 2-chloro-4-fluorophenyl, 2,4-dichlorophenyl, —CH2C(CH3)3, —C(CH3)2CF3,
—C(CH3)2CH2CH3, —C(CH3)2CF2CH3, —C(CH3)2CH2CF3, —C(CH3)3,
or CF3.
In a further aspect, in the compounds of formulas (I), (II) and/or (III), R2 is
three of X1, X2, X3, and X4 are CH, while one of X1, X2, X3, and X4 is N; A-(R1)n is
where R1 is halogen,
—CH2C(CH3)3, 2-chloro-4-fluorophenyl, 2,4-dichlorophenyl, —CH2C(CH3)3, —C(CH3)2CF3,
—C(CH3)2CH2CH3, —C(CH3)2CF2CH3, —C(CH3)2CH2CF3, —C(CH3)3,
or CF3.
In a further aspect, in the compounds of formulas (I), (II) and/or (III), R2 is —CH(CH3)CF2D, —CH(CD3)2, —CH(CF3)CD3, —CH(CH3)CDF2, —CD(CD3)2, or —CD(CH3)CD3; X1, X2, X3, and X4 are CH; A-(R1)n is
where R1 is halogen,
—CH2C(CH3)3, 2-chloro-4-fluorophenyl, 2,4-dichlorophenyl, —CH2C(CH3)3, —C(CH3)2CF3,
—C(CH3)2CH2CH3, —C(CH3)2CF2CH3, —C(CH3)2CH2CF3, —C(CH3)3,
or CF3.
In a yet still further aspect, in the compounds of formulas (I), (II) and/or (III), R2 is —CH(CH3)CF2D, —CH(CD3)2, —CH(CF3)CD3, —CH(CH3)CDF2, —CD(CD3)2, or —CD(CH3)CD3; three of X1, X2, X3, and X4 are CH, while one of X1, X2, X3, and X4 is N; A-(R1)n is
where R1 is halogen,
—CH2C(CH3)3, 2-chloro-4-fluorophenyl, 2,4-dichlorophenyl, —CH2C(CH3)3, —C(CH3)2CF3,
—C(CH3)2CH2CH3, —C(CH3)2CF2CH3, —C(CH3)2CH2CF3, —C(CH3)3,
or CF3.
In another aspect, in the compounds of formulas (I), (II) and/or (III), R2 is isopropyl; X1, X2, X3, and X4 are CH; A-(R1)n is
where at least one R1 is halogen
—CH2C(CH3)3, 2-chloro-4-fluorophenyl, 2,4-dichlorophenyl, —CH2C(CH3)3, —C(CH3)2CF3,
—C(CH3)2CH2CH3, —C(CH3)2CF2CH3, —C(CH3)2CH2CF3, —C(CH3)3,
or CF3.
In an aspect, in the compounds of formulas (I), (II) and/or (III), R2 is isopropyl; three of X1, X2, X3, and X4 are CH, while one of X1, X2, X3, and X4 is N; A-(R1)n is
where at least one R1 is halogen,
—CH2C(CH3)3, 2-chloro-4-fluorophenyl, 2,4-dichlorophenyl, —CH2C(CH3)3, —C(CH3)2CF3,
—C(CH3)2CH2CH3, —C(CH3)2CF2CH3, —C(CH3)2CH2CF3, —C(CH3)3,
or CF3.
In an aspect, in the compounds of formulas (I), (II) and/or (III), R2 is
X1, X2, X3, and X4 are CH; A-(R1)n is
where at least one R1 is halogen,
—CH2C(CH3)3, 2-chloro-4-fluorophenyl, 2,4-dichlorophenyl, —CH2C(CH3)3, —C(CH3)2CF3,
—C(CH3)2CH2CH3, —C(CH3)2CF2CH3, —C(CH3)2CH2CF3, —C(CH3)3,
or CF3.
In a further aspect, in the compounds of formulas (I), (II) and/or (III), R2 is
three of X1, X2, X3, and X4 are CH, while one of X1, X2, X3, and X4 is N; A-(R1)n is
where at least one R1 is halogen,
—CH2C(CH3)3, 2-chloro-4-fluorophenyl, 2,4-dichlorophenyl, —CH2C(CH3)3, —C(CH3)2CF3,
—C(CH3)2CH2CH3, —C(CH3)2CF2CH3, —C(CH3)2CH2CF3, —C(CH3)3,
or CF3.
In a further aspect, in the compounds of formulas (I), (II) and/or (III), R2 is —CH(CH3)CF2D, —CH(CD3)2, —CH(CF3)CD3, —CH(CH3)CDF2, —CD(CD3)2, or —CD(CH3)CD3; X1, X2, X3, and X4 are CH; A-(R1)n is
where at least one R1 is halogen,
—CH2C(CH3)3, 2-chloro-4-fluorophenyl, 2,4-dichlorophenyl, —CH2C(CH3)3, —C(CH3)2CF3,
—C(CH3)2CH2CH3, —C(CH3)2CF2CH3, —C(CH3)2CH2CF3, —C(CH3)3,
or CF3.
In a yet still further aspect, in the compounds of formulas (I), (II) and/or (III), R2 is —CH(CH3)CF2D, —CH(CD3)2, —CH(CF3)CD3, —CH(CH3)CDF2, —CD(CD3)2, or —CD(CH3)CD3; three of X1, X2, X3, and X4 are CH, while one of X1, X2, X3, and X4 is N; A-(R1)n is
where at least one R1 is halogen,
—CH2C(CH3)3, 2-chloro-4-fluorophenyl, 2,4-dichlorophenyl, —CH2C(CH3)3, —C(CH3)2CF3,
—C(CH3)2CH2CH3, —C(CH3)2CF2CH3, —C(CH3)2CH2CF3, —C(CH3)3,
or CF3.
In one aspect, in the compounds of formulas (I), (II) and/or (III), R2 is isopropyl; X1, X2, X3, and X4 are CH; A-(R1)n is
where at least one R1 is halogen,
—CH2C(CH3)3, 2-chloro-4-fluorophenyl, 2,4-dichlorophenyl, —CH2C(CH3)3, —C(CH3)2CF3,
—C(CH3)2CH2CH3, —C(CH3)2CF2CH3, —C(CH3)2CH2CF3, —C(CH3)3,
or CF3.
In another aspect, in the compounds of formulas (I), (II) and/or (III), R2 is isopropyl; three of X1, X2, X3, and X4 are CH, while one of X1, X2, X3, and X4 is N; A-(R1)n is
where at least one R1 is halogen,
—CH2C(CH3)3, 2-chloro-4-fluorophenyl, 2,4-dichlorophenyl, —CH2C(CH3)3, —C(CH3)2CF3
—C(CH3)2CH2CH3, —C(CH3)2CF2CH3, —C(CH3)2CH2CF3, —C(CH3)3,
or CF3.
In an aspect, in the compounds of formulas (I), (II) and/or (III), R2 is
X1, X2, X3, and X4 are CH; A-(R1)n is
where at least one R1 is halogen,
—CH2C(CH3)3, 2-chloro-4-fluorophenyl, 2,4-dichlorophenyl, —CH2C(CH3)3, —C(CH3)2CF3,
—C(CH3)2CH2CH3, —C(CH3)2CF2CH3, —C(CH3)2CH2CF3, —C(CH3)3,
or CF3.
In a further aspect, in the compounds of formulas (I), (II) and/or (III), R2 is
three of X1, X2, X3, and X4 are CH, while one of X1, X2, X3, and X4 is N; A-(R1)n is
where at least one R1 is halogen,
—CH2C(CH3)3, 2-chloro-4-fluorophenyl, 2,4-dichlorophenyl, —CH2C(CH3)3, —C(CH3)2CF3,
—C(CH3)2CH2CH3, —C(CH3)2CF2CH3, —C(CH3)2CH2CF3, —C(CH3)3,
or CF3.
In a further aspect, in the compounds of formulas (I), (II) and/or (III), R2 is —CH(CH3)CF2D, —CH(CD3)2, —CH(CF3)CD3, —CH(CH3)CDF2, —CD(CD3)2, or —CD(CH3)CD3; X1, X2, X3, and X4 are CH; A-(R1)n is
where at least one R1 is halogen,
—CH2C(CH3)3, 2-chloro-4-fluorophenyl, 2,4-dichlorophenyl, —CH2C(CH3)3, —C(CH3)2CF3,
—C(CH3)2CH2CH3, —C(CH3)2CF2CH3, —C(CH3)2CH2CF3, —C(CH3)3,
or CF3.
In a yet still further aspect, in the compounds of formulas (I), (II) and/or (III), R2 is —CH(CH3)CF2D, —CH(CD3)2, —CH(CF3)CD3, —CH(CH3)CDF2, —CD(CD3)2, or —CD(CH3)CD3; three of X1, X2, X3, and X4 are CH, while one of X1, X2, X3, and X4 is N; A-(R1)n is
where at least one R1 is halogen,
—CH2C(CH3)3, 2-chloro-4-fluorophenyl, 2,4-dichlorophenyl, —CH2C(CH3)3, —C(CH3)2CF3,
—C(CH3)2CH2CH3, —C(CH3)2CF2CH3, —C(CH3)2CH2CF3, —C(CH3)3,
or CF3.
In another aspect, in the compounds of formulas (I), (II) and/or (III), R2 is isopropyl; X1, X2, X3, and X4 are CH; A-(R1)n is
where R1 is halogen,
—CH2C(CH3)3, 2-chloro-4-fluorophenyl, 2,4-dichlorophenyl, —CH2C(CH3)3, —C(CH3)2CF3,
—C(CH3)2CH2CH3, —C(CH3)2CF2CH3, —C(CH3)2CH2CF3, —C(CH3)3,
or CF3.
In an aspect, in the compounds of formulas (I), (II) and/or (III), R2 is isopropyl; three of X1, X2, X3, and X4 are CH, while one of X1, X2, X3, and X4 is N; A-(R1)n is
where R1 is halogen,
—CH2C(CH3)3, 2-chloro-4-fluorophenyl, 2,4-dichlorophenyl, —CH2C(CH3)3, —C(CH3)2CF3,
—C(CH3)2CH2CH3, —C(CH3)2CF2CH3, —C(CH3)2CH2CF3, —C(CH3)3,
or CF3.
In an aspect, in the compounds of formulas (I), (II) and/or (III), R2 is
X1, X2, X3, and X4 are CH; A-(R1)n is
where R1 is halogen,
—CH2C(CH3)3, 2-chloro-4-fluorophenyl, 2,4-dichlorophenyl, —CH2C(CH3)3, —C(CH3)2CF3,
—C(CH3)2CH2CH3, —C(CH3)2CF2CH3, —C(CH3)2CH2CF3, —C(CH3)3,
or CF3.
In a further aspect, in the compounds of formulas (I), (II) and/or (III), R2 is
three of X1, X2, X3, and X4 are CH, while one of X1, X2, X3, and X4 is N; A-(R1)n is
where R1 is halogen,
—CH2C(CH3)3, 2-chloro-4-fluorophenyl, 2,4-dichlorophenyl, —CH2C(CH3)3, —C(CH3)2CF3,
—C(CH3)2CH2CH3, —C(CH3)2CF2CH3, —C(CH3)2CH2CF3, —C(CH3)3,
or CF3.
In a further aspect, in the compounds of formulas (I), (II) and/or (III), R2 is —CH(CH3)CF2D, —CH(CD3)2, —CH(CF3)CD3, —CH(CH3)CDF2, —CD(CD3)2, or —CD(CH3)CD3; X1, X2, X3, and X4 are CH; A-(R1)n is
where R1 is halogen,
—CH2C(CH3)3, 2-chloro-4-fluorophenyl, 2,4-dichlorophenyl, —CH2C(CH3)3, —C(CH3)2CF3,
—C(CH3)2CH2CH3, —C(CH3)2CF2CH3, —C(CH3)2CH2CF3, —C(CH3)3,
or CF3.
In a yet still further aspect, in the compounds of formulas (I), (II) and/or (III), R2 is —CH(CH3)CF2D, —CH(CD3)2, —CH(CF3)CD3, —CH(CH3)CDF2, —CD(CD3)2, or —CD(CH3)CD3; three of X1, X2, X3, and X4 are CH, while one of X1, X2, X3, and X4 is N; A-(R1)n is
where R1 is halogen,
—CH2C(CH3)3, 2-chloro-4-fluorophenyl, 2,4-dichlorophenyl, —CH2C(CH3)3, —C(CH3)2CF3,
—C(CH3)2CH2CH3, —C(CH3)2CF2CH3, —C(CH3)2CH2CF3, —C(CH3)3,
or CF3.
In one aspect, in the compounds of formulas (I), (II) and/or (III), R2 is isopropyl; X1, X2, X3, and X4 are CH; A-(R1)n is
where each R1 is halogen,
—CH2C(CH3)3, 2-chloro-4-fluorophenyl, 2,4-dichlorophenyl, —CH2C(CH3)3, —C(CH3)2CF3,
—C(CH3)2CH2CH3, —C(CH3)2CF2CH3, —C(CH3)2CH2CF3, —C(CH3)3,
or CF3.
In another aspect, in the compounds of formulas (I), (II) and/or (III), R2 is isopropyl; three of X1, X2, X3, and X4 are CH, while one of X1, X2, X3, and X4 is N; A-(R1)n is
where each R1 is halogen,
—CH2C(CH3)3, 2-chloro-4-fluorophenyl, 2,4-dichlorophenyl, —CH2C(CH3)3, —C(CH3)2CF3,
—C(CH3)2CH2CH3, —C(CH3)2CF2CH3, —C(CH3)2CH2CF3, —C(CH3)3,
or CF3.
In an aspect, in the compounds of formulas (I), (II) and/or (III), R2 is
X1, X2, X3, and X4 are CH; A-(R1)n is
where each R1 is halogen,
—CH2C(CH3)3, 2-chloro-4-fluorophenyl, 2,4-dichlorophenyl, —CH2C(CH3)3, —C(CH3)2CF3,
—C(CH3)2CH2CH3, —C(CH3)2CF2CH3, —C(CH3)2CH2CF3, —C(CH3)3,
or CF3.
In a further aspect, in the compounds of formulas (I), (II) and/or (III), R2 is
three of X1, X2, X3, and X4 are CH, while one of X1, X2, X3, and X4 is N; A-(R1)n is
where each R1 is halogen,
—CH2C(CH3)3, 2-chloro-4-fluorophenyl, 2,4-dichlorophenyl, —CH2C(CH3)3, —C(CH3)2CF3,
—C(CH3)2CH2CH3, —C(CH3)2CF2CH3, —C(CH3)2CH2CF3, —C(CH3)3,
or CF3.
In a further aspect, in the compounds of formulas (I), (II) and/or (III), R2 is —CH(CH3)CF2D, —CH(CD3)2, —CH(CF3)CD3, —CH(CH3)CDF2, —CD(CD3)2, or —CD(CH3)CD3; X1, X2, X3, and X4 are CH; A-(R1)n is
where each R1 is halogen
—CH2C(CH3)3, 2-chloro-4-fluorophenyl, 2,4-dichlorophenyl, —CH2C(CH3)3, —C(CH3)2CF3,
—C(CH3)2CH2CH3, —C(CH3)2CF2CH3, —C(CH3)2CH2CF3, —C(CH3)3,
or CF3.
In a yet still further aspect, in the compounds of formulas (I), (II) and/or (III), R2 is —CH(CH3)CF2D, —CH(CD3)2, —CH(CF3)CD3, —CH(CH3)CDF2, —CD(CD3)2, or —CD(CH3)CD3; three of X1, X2, X3, and X4 are CH, while one of X1, X2, X3, and X4 is N; A-(R1)n is
where each R1 is halogen,
—CH2C(CH3)3, 2-chloro-4-fluorophenyl, 2,4-dichlorophenyl, —CH2C(CH3)3, —C(CH3)2CF3,
—C(CH3)2CH2CH3, —C(CH3)2CF2CH3, —C(CH3)2CH2CF3, —C(CH3)3,
or CF3.
Whenever a variable is defined as “each,” for example, “each R1 is . . . ” it is understood that the definition of the variable at each occurrence is independently selected from the groups contained in the definition. Thus, for example, if a phenyl is substituted with four R1 groups, the identity of each R1 group is independently selected from the groups listed in the definition of R1. Accordingly, all four R1 groups may be the same or they may all be different or some of the groups may be the same, while others are different.
Specific enantiomers may be prepared beginning with chiral reagents or by stereo-selective or stereo-specific synthetic techniques. Alternatively, single enantiomers may be isolated from mixtures of different chiral forms by standard chiral chromatographic or crystallization techniques at any convenient point in the synthesis of compounds of formula (I), formula (II), and formula (III). All individual enantiomers, as well as mixtures of the enantiomers of the compounds of formula (II) and formula (III) including racemates are intended to be included herein.
Specific examples of the compounds of formula (I) including the forms of formula (II) and formula (III) are shown in the Examples below. A subset of useful molecules from the Examples is shown in Table A.
The structures drawn in Table A do not indicate absolute stereochemistry at the backbone chiral position (shown by ϕ in formula (I)ϕ). However, the isomers can be separated by chiral chromatography as described in the Examples below and differing activity is often noted between the isomers. Thus, in each of the Examples in Table A, the noted isomer (i.e., Isomer 1 or Isomer 2) could be the R-enantiomeric form as differentiated over the S-enantiomeric form (or vice versa) of the molecule. Both the R-enantiomeric form and the S-enantiomeric form are indicated below in the examples and both forms are intended to be included in the disclosure herein.
Compounds of formula (I) including the forms of formula (II) and formula (III) also can be deuterated at specific positions and such deuterated forms are understood to be disclosed herein where a hydrogen can be replaced by a deuterium in a disclosed molecule.
The compounds of formulas (I), (II), and (III) described herein may form pharmaceutically acceptable salts. Such pharmaceutically acceptable salts of the compounds of formulas (I), (II), and (III) are intended to be included. Pharmaceutically acceptable salts and common methodology for preparing them are well known in the art (see, e.g., P. Stahl, et al. Handbook of Pharmaceutical Salts; Properties, Selection and Use, 2nd Revised Edition (Wiley-VCH, 2011); S. M. Berge, et al., “Pharmaceutical Salts,” Journal of Pharmaceutical Sciences, Vol. 66, No. 1, January 1977).
The compounds of formulas (I), (II), and (III) as described herein are generally effective over a wide dosage range. For example, dosages per day fall within the range of about 1 mg/kg to about 200 mg/kg. Further, the compounds of formulas (I), (II), and (III) as described herein can be administered, for example, in an amount of about 1 mg/kg to about 150 mg/kg, about 1 mg/kg to about 100 mg/kg, about 5 mg/kg to about 150 mg/kg, about 5 mg/kg to about 100 mg/kg, about 20 mg/kg to about 40 mg/kg, about 25 mg/kg to about 35 mg/kg, about 50 mg/kg to about 70 mg/kg, about 55 mg/kg to about 65 mg/kg, about 90 mg/kg to about 110 mg/kg, about 95 mg/kg to about 105 mg/kg, or about 50 mg/kg to about 150 mg/kg. Additionally, the compounds of formulas (I), (II), and (III) as described herein can be administered, for example, in an amount of about 5 mg/kg, about 10 mg/kg, about 15 mg/kg, about 20 mg/kg, about 25 mg/kg, about 30 mg/kg, about 35 mg/kg, about 40 mg/kg, about 45 mg/kg, about 50 mg/kg, about 55 mg/kg, about 60 mg/kg, about 65 mg/kg, about 70 mg/kg, about 75 mg/kg, about 80 mg/kg, about 85 mg/kg, about 90 mg/kg, about 95 mg/kg, about 100 mg/kg, about 105 mg/kg, about 110 mg/kg, about 115 mg/kg, about 120 mg/kg, about 125 mg/kg, about 130 mg/kg, about 135 mg/kg, about 140 mg/kg, about 145 mg/kg, about 150 mg/kg, about 155 mg/kg, about 160 mg/kg, about 165 mg/kg, about 170 mg/kg, about 175 mg/kg, about 180 mg/kg, about 185 mg/kg, about 190 mg/kg, about 195 mg/kg, or about 200 mg/kg. Daily administration can be once-daily or in multiple doses, e.g., twice-daily (BID) administration. It will be understood that the amount of a compound actually administered will be determined by a physician, in light of the relevant circumstances, including the condition to be treated, the chosen route of administration, the actual compound or compounds administered, the age, weight, and response of the individual patient, and the severity of the patient's symptoms.
The compounds of formulas (I), (II), and (III) as described herein can be formulated as pharmaceutical compositions that can be administered by a variety of routes. Such pharmaceutical compositions and processes for preparing the same are well known in the art (see, e.g., Remington; The Science and Practice of Pharmacy (A. Gennaro, et al., eds., 21st ed., Mack Publishing Co., 2005)). Specifically, the compounds of formulas (I), (II), and (III), as described herein, or pharmaceutically acceptable salts thereof, can be combined with one or more pharmaceutically acceptable carriers, diluents, or excipients. More particularly, the compounds described herein by formulas (I), (II), and (III) can be formulated as pharmaceutical compositions. Further, the compounds of formulas (I), (II), and (III) as described herein, or pharmaceutically acceptable salts thereof, can be combined with one or more other therapeutic agents. For example, the compounds of formulas (I), (II), and (III) as described herein, or pharmaceutically acceptable salts thereof, can be a component in a pharmaceutical composition for the treatment of cancer in combination with one or more pharmaceutically acceptable carriers, diluents, or excipients, and optionally with one or more additional therapeutic agents. Pharmaceutical compositions containing the compounds of formulas (I), (II), and (III) as described herein, or pharmaceutically acceptable salts thereof, can be used in the methods described herein.
The term “treating” (or “treat” or “treatment”) as used herein refers to restraining, slowing, stopping, or reversing the progression or severity of an existing symptom, condition or disorder.
As used herein, the term “irritable bowel syndrome” or “IBS” means gastrointestinal disorders including, but not limited to, diarrhea-predominant, constipation-predominant or alternating stool pattern, functional bloating, functional constipation, functional diarrhea, unspecified functional bowel disorder, functional abdominal pain syndrome, chronic idiopathic constipation, functional esophageal disorders, functional gastroduodenal disorders, functional anorectal pain, and inflammatory bowel disease.
As used herein, the terms “cancer” and “cancerous” refer to or describe the physiological condition in patients that is typically characterized by unregulated cell proliferation. Included in this definition are benign and malignant cancers. By “early stage cancer” or “early stage tumor” is meant a cancer that is not advanced or metastatic or is classified as a Stage 0, I, or II cancer. Examples of cancer include, but are not limited to, lung cancer (e.g., small cell lung carcinoma or non-small cell lung carcinoma), thyroid cancer (e.g., papillary thyroid cancer, medullary thyroid cancer, differentiated thyroid cancer, recurrent thyroid cancer, or refractory differentiated thyroid cancer), thyroid adenoma, endocrine gland neoplasms, lung adenocarcinoma, bronchioles lung cell carcinoma, multiple endocrine neoplasia type 2A or 2B (MEN2A or MEN2B, respectively), pheochromocytoma, parathyroid hyperplasia, breast cancer, mammary cancer, mammary carcinoma, mammary neoplasm, colorectal cancer (e.g., metastatic colorectal cancer), papillary renal cell carcinoma, ganglioneuromatosis of the gastroenteric mucosa, inflammatory myofibroblastic tumor, and cervical cancer.
The term “RET-associated disease or disorder” as used herein refers to diseases or disorders associated with or having a dysregulation of a RET gene, a RET kinase (also called herein RET kinase protein), or the expression or activity or level of any (e.g., one or more) of the same (e.g., any of the types of dysregulation of a RET gene, a RET kinase, a RET kinase domain, or the expression or activity or level of any of the same described herein).
The term “RET-associated cancer” as used herein refers to cancers associated with or having a dysregulation of a RET gene, a RET kinase (also called herein RET kinase protein), or expression or activity, or level of any of the same. Non-limiting examples of a RET-associated cancer are described herein.
The phrase “dysregulation of a RET gene, a RET kinase, or the expression or activity or level of any of the same” refers to a genetic mutation. Examples of such genetic mutations causing dysregulation of a RET gene, a RET kinase, or the expression or activity or level of any of the same include, but are not limited to, a RET gene translocation that results in the expression of a fusion protein, a deletion in a RET gene that results in the expression of a RET protein that includes a deletion of at least one amino acid as compared to the wild-type RET protein, a mutation in a RET gene that results in the expression of a RET protein with one or more point mutations, or an alternative spliced version of a RET mRNA that results in a RET protein having a deletion of at least one amino acid in the RET protein as compared to the wild-type RET protein or a RET gene amplification that results in overexpression of a RET protein or an autocrine activity resulting from the overexpression of a RET gene in a cell that results in a pathogenic increase in the activity of a kinase domain of a RET protein (e.g., a constitutively active kinase domain of a RET protein) in a cell. A dysregulation of a RET gene, a RET protein, or expression or activity, or level of any of the same, can be a mutation in a RET gene that encodes a RET protein that is constitutively active or has increased activity as compared to a protein encoded by a RET gene that does not include the mutation. For example, a dysregulation of a RET gene, a RET protein, or expression or activity, or level of any of the same, can be the result of a gene or chromosome translocation which results in the expression of a fusion protein that contains a first portion of RET that includes a functional kinase domain, and a second portion of a partner protein (i.e., that is not RET). In some examples, dysregulation of a RET gene, a RET protein, or expression or activity or level of any of the same can be a result of a gene translocation of one RET gene with another non-RET gene.
Methods for the treatment of RET-associated diseases or disorders, in particular for the treatment of IBS or cancer with abnormal RET expression, using the compounds of formulas (I), (II), and (III) as described herein are provided. Examples of cancers with abnormal RET expression include cancers caused by dysregulation of a RET gene, a RET kinase, or the expression or activity or level of any of the same. One such method of treating RET-associated diseases or disorders such as IBS or cancer includes administering a therapeutically effective amount of to a patient in need thereof. Another method of treating RET-associated diseases or disorders such as IBS or cancer includes a) detecting a dysregulation of a RET gene, a RET kinase, or the expression or activity or level of any of the same in a sample from the patient; and b) administering a therapeutically effective amount of a compound of formula I or a pharmaceutically acceptable salt.
The dysregulation of a RET gene, a RET kinase, or the expression or activity or level of any of the same can be the result of one or more chromosome translocations or inversions resulting in a RET gene fusion (i.e., the genetic translocations result in an expressed protein that is a fusion protein containing residues from a non-RET partner protein and including a minimum of a functional RET kinase domain). Non-limiting examples of RET fusion partners and their associated cancers include ACBD5 (papillary thyroid cancer); AFAP1 (NSCLC); AFAP1L2 (papillary thyroid cancer); AKAP13 (papillary thyroid cancer); BCR (chronic myelomonocytic leukemia); C10orf118 (papillary thyroid cancer); CCDCl6 (also called PTC1, D10S170, or H4) (NSCLC, colon cancer, papillary thyroid cancer, adenocarcinomas, lung adenocarcinoma, metastatic colorectal cancer, adenosquamous carcinomas, breast cancer); CCDCl88C (NSCLC); CEP55 (diffuse gastric cancer); CGNL1 (pancreatic cancer); CLIP1 (adenocarcinoma); CUX1 (lung adenocarcinoma); DLG5 (non-anaplastic thyroid cancer); DOCK1 (NSCLC); EML4 (papillary thyroid cancer); ERC1 (also called ELKS) (papillary thyroid cancer, breast cancer); ETV6 (salivary cancer); FGFR1OP (CMML, primary myelofibrosis with secondary acute myeloid leukemia); FKBP15 (papillary thyroid cancer); FOXP4 (lung adenocarcinoma); FRMD4A (NSCLC); GOLGA5 (also called PTC5) (papillary thyroid cancer, spitzoid neoplasms); H4L (various); HOOK3 (papillary thyroid cancer); HRH4-RET (thyroid cancer and/or papillary thyroid cancer); HTIF1 (various); KIAA1217 (also called SKT) (papillary thyroid cancer, lung adenocarcinoma, NSCLC); KIAA1468 (also called PTC9 and RFG9) (papillary thyroid cancer, lung adenocarcinoma); KIF13A (NSCLC); KIF5B (NSCLC, ovarian cancer, spitzoid neoplasms, lung adenocarcinoma, adenosquamous carcinomas); KTN1 (also called PTC8) (papillary thyroid cancer); MBD1 (also known as PCM1) (papillary thyroid cancer); MPRIP (NSCLC); MYH10 (infantile myofibromatosis); MYH13 (medullary thyroid cancer); NCOA4 (also called PTC3, ELE1, and RFG) (papillary thyroid cancer, NSCLC, colon cancer, salivary gland cancer, metastatic colorectal cancer, lung adenocarcinoma, adenosquamous carcinomas diffuse sclerosing variant of papillary thyroid cancer, breast cancer, acinic cell cancer, mammary analog secretory cancer); OLFM4 (Small-bowel cancer); PARD3 (NSCLC); PCM1 (papillary thyroid cancer); PIBF1 (bronchiolus lung cell cancer); PICALM (NSCLC); PPFIBP2 (papillary thyroid cancer); PRKAR1A (also called PTC2) (papillary thyroid cancer); PTClex9 (a novel CCDC6 rearrangement) (metastatic papillary thyroid cancer); PTC4 (a novel NCO4/ELE1 rearrangement) (papillary thyroid cancer); RAB61P2 (papillary thyroid cancer); RASAL2 (Sarcoma); RASGEF1A (breast cancer); RBPMS (NSCLC); RFG8 (papillary thyroid cancer); RRBP1 (colon cancer); RUFY1 (colorectal cancer); RUFY2 (NSCLC; papillary thyroid cancer); RUFY3 (papillary thyroid cancer); SLC12A2 (NSCLC); SORBS2 (papillary thyroid cancer); SPECC1L (papillary thyroid cancer; thyroid gland cancer); SQSTM1 (papillary thyroid cancer); TAF3 (pancreatic cancer); TBL1XR1 (papillary thyroid cancer, thyroid gland cancer); TFG (pancreatic cancer); TIF1G (various); TRIM24 (also called PTC6) (papillary thyroid cancer); TRIM27 (also called RFP) (papillary thyroid cancer); AKAP13 (papillary thyroid cancer); TRIM33 (also called PTC7 and RFG7) (NSCLC, papillary thyroid cancer); and UEVLD (papillary thyroid cancer). The fusion protein can be, for example, KIF5B-RET. Other RET fusion proteins may not be included in the listing herein or are not yet known; however, the compounds of formulas (I), (II), and (III) and methods for their use as described herein are expected to be effective inhibitors.
The dysregulation of a RET gene, a RET kinase, or expression or activity or level of any of the same, can be caused by one or more point mutations, insertions, or deletions in a RET gene (compared to wildtype RET). For reference, the sequence of mature human RET protein (SEQ ID NO: 1) is provided here:
Non-limiting examples of activating RET kinase protein point mutations, insertions, or deletions as compared to wild-type RET kinase can occur at the following amino acid positions: 2, 3, 4, 5, 6, 7, 8, 11, 12, 13, 20, 32 (e.g., S32L), 34 (e.g., D34S), 40 (e.g., L40P), 56 (e.g., L56M), 64 (e.g., P64L), 67 (e.g., R67H), 114 (e.g., R114H), 136 (e.g., glutamic acid to stop codon), 145 (e.g., V145G), Amino acid position 180 (e.g., arginine to stop codon), 200, 292 (e.g., V292M), 294, 321 (e.g., G321R), 330 (e.g., R330Q), 338 (e.g., T338I), 360 (e.g., R360W), 373 (e.g., alanine to frameshift), 393 (e.g., F393L), 423 (e.g., G423R), 432, 446 (e.g., G446R), 505-506 (6-Base Pair In-Frame Germline Deletion in Exon 7), 510 (e.g., A510V), 511 (e.g., E511K), 513 (e.g., G513D), (e.g., C515R, C515S, C515W), 525 (e.g., R525W), 531 (e.g., C531R, or 9 base pair duplication), 532 (e.g., duplication), 533 (e.g., G533C, G533S), 550 (e.g., G550E), 591 (e.g., V591I), 593 (e.g., G593E), 595 (e.g., E595D and E595A), 600 (e.g., R600Q), 602 (e.g., 1602V), 603 (e.g., K603Q, K603E), 606 (e.g., Y606C), 609 (e.g., C609Y, C609S, C609G, C609R, C609F, C609W, C609C), 611 (e.g., C611R, C611S, C611G, C611Y, C611F, C611W), 616 (e.g., E616Q), 618 (e.g., C618S, C618Y, C618R, C618T, C618G, C618F, C618W), 620 (e.g., C620S, C620W, C620R, C620G, C620L, C620Y, C620F), (e.g., E623K), 624 (e.g., D624N), 630 (e.g., C630A, C630R, C630S, C630Y, C630F, C630W, C630G), 631 (e.g., D631N, D631Y, D631A, D631G, D631V, D631E), 632 (e.g., E632K, E632G), 632-633 (6-Base Pair In-Frame Germline Deletion in Exon 11), 633 (e.g., 9 base pair duplication), 634 (e.g., C634W, C634Y, C634S, C634R, C634F, C634G, C634L, C634A, or C634T, or an insertion ELCR, or a 12 base pair duplication, or in combination with A640G, A641A, or A641T) (e.g., causing MTC), 634/852 (e.g., C634R/I852M), 635 (e.g., R635G), 636 (e.g., T636P, T636M), 648 (e.g., V648I), 649 (e.g., S649L), 664 (e.g., A664D), 665 (e.g., H665Q), 666 (e.g., K666E, K666M, K666N, K666R), 675 (T675T, silent nucleotide change), 686 (e.g., S686N), 689 (e.g., S689T), (e.g., G691S), 694 (e.g., R694Q), 700 (e.g., M700L), 706 (e.g., V706M, V706A), splice variant (e.g., E713K), 732 (e.g., E732K), 736 (e.g., G736R), 748 (e.g., G748C), 765 (e.g., S765P), 766 (e.g., P766S, P766M6), 768 (e.g., E768Q, E768D), 769 (e.g., L769L), 770 (e.g., R770Q), 771 (e.g., D771N), 777 (e.g., N777S), 778 (e.g., V778I), 781 (e.g., Q781R), 788 (e.g., I788I), 790 (e.g., L790F, L790T), 791 (e.g., Y791F, Y791N), 791/852 (e.g., Y791F/I852M), 802, 804 (e.g., V804L, V804M, V804E, V804G, V804S) (e.g., causing MTC), 804/918 (e.g., V804M/M918T, V804L/M918T), 805 (e.g., E805K), 804/805 (e.g., V804M/E805K), 806 (e.g., Y806F, Y806C, Y806H, Y806Y), 810 (e.g., G810R, G810S, G810A, G810C, G810V), 818 (e.g., E818K), 819 (e.g., S819I), 823 (e.g., G823E), 826 (e.g., Y826M, Y826S), 833 (e.g., R833C), 841 (e.g., P841L, P841P), (e.g., E843D), 844 (e.g., R844W, R844Q, R844L), 848 (e.g., M848T), 852 (e.g., I852M), 865 (e.g., L865V), 870 (e.g., L870F), 873 (e.g., R873W), 876 (e.g., A876V), 881 (e.g., L881V), 882, 883 (e.g., A883F, A883P, A883S, A883T, A883Y), 884 (e.g., E884K), 886 (e.g., R886W), 891 (e.g., S891A), 897 (e.g., R897Q), 898 (e.g., D898V), (e.g., Y900F), 901 (e.g., E901K), 904 (e.g., S904F, S904C), 905 (e.g., Y905F), 907 (e.g., K907E, K907M), 908 (e.g., R908K), 911 (e.g., G911D), 912 (e.g., R912P, R912Q), (e.g., M918T, M918V, M918L, M918R) (e.g., causing MTC), 919 (e.g., A919V), (e.g., E921K), 922 (e.g., S922P, S922Y), 930 (e.g., T930M), 961 (e.g., F961L), 972 (e.g., R972G), 981 (e.g., Y981F), 982 (e.g., R982C), 1009 (e.g., M1009V), 1015 (e.g., Y1015F), 1017 (e.g., D1017N), 1041 (e.g., V1041G), 1064 (e.g., M1064T), 1096 (e.g., Y1096F), RET+3, In-Frame Deletion in Exons 6 and 11, 3 bp In-Frame Deletion in Exon 15, Nucleotide position 2136+2 (e.g., 2136+2T>G), del632-636 ins6. The RET kinase protein point mutations/insertions/deletions can be, for example, M918T, M918V, C634W, V804L, or V804M. Other RET kinase protein point mutations/insertions/deletions may not be included in the listing herein or are not yet known; however, the compounds of formulas (I), (II), and (III) and methods for their use as described herein are expected to be effective inhibitors.
A dysregulation of a RET gene, a RET kinase, or expression or activity or level of any of the same, can also include a splice variation in a RET mRNA which results in an expressed protein that is an alternatively spliced variant of RET having at least one residue deleted (as compared to the wild-type RET kinase) resulting in a constitutive activity of a RET kinase domain.
A “RET kinase inhibitor” as defined herein refers to compounds that inhibit RET activity using a measurement such as the Biological Assays described below in the examples.
In some cases, a RET kinase containing a mutation, insertion, or deletion is more resistant to inhibition of its phosphotransferase activity by one or more first RET kinase inhibitor(s), as compared to a wildtype RET kinase or a RET kinase not including the same mutation. Such mutations may not decrease the sensitivity of the cancer cell or tumor having the RET kinase to treatment a compound of formulas (I), (II), and (III) as described herein (e.g., as compared to a cancer cell or a tumor that does not include the particular RET inhibitor resistance mutation). In these cases, a RET inhibitor resistance mutation can result in a RET kinase that has one or more of an increased Vmax, a decreased Km for ATP, and an increased KD for a first RET kinase inhibitor, when in the presence of a first RET kinase inhibitor, as compared to a wildtype RET kinase or a RET kinase not having the same mutation in the presence of the same first RET kinase inhibitor.
In other cases, a RET kinase containing a mutation, insertion, or deletion, has increased resistance to a compound of formulas (I), (II), and (III) as described herein, as compared to a wildtype RET kinase or a RET kinase not including the same mutation. In such cases, a RET inhibitor resistance mutation can result in a RET kinase that has one or more of an increased Vmax, a decreased Km, and a decreased KD in the presence of a compound of formulas (I), (II), and (III) as described herein, as compared to a wildtype RET kinase or a RET kinase not having the same mutation in the presence of the same compound of formulas (I), (II), and (III) as described herein.
Examples of RET inhibitor resistance mutations can include point mutations, insertions, or deletions in and near the ATP binding site in the tertiary structure of RET kinase, including, but not limited to, the gatekeeper residue, P-loop residues, residues in or near the DFG motif, and ATP cleft solvent front amino acid residues. Additional examples of these types of mutations include changes in residues that may affect enzyme activity and/or drug binding including but are not limited to residues in the activation loop, residues near or interacting with the activation loop, residues contributing to active or inactive enzyme conformations, changes including mutations, deletions, and insertions in the loop proceeding the C-helix and in the C-helix. Specific residues or residue regions that at which mutations are known to create RET inhibitor resistance include but are not limited to the following amino acids (based on the human wildtype RET protein sequence (SEQ ID NO: 1)): 732 (e.g., E732K); 788 (e.g., I788N); 804 (e.g., V804M, V804L, V804E); 804/805 (e.g., V804M/E805K); 806 (e.g., Y806C, Y806E, Y806S, Y806H, Y806N); 810 (e.g., G810A, G810C, G810R, G810S, G810V); and 865 (e.g., L865V). Further examples of RET inhibitor resistance mutation positions include, but are not limited to, the following amino acids (based on the human wildtype RET protein sequence (SEQ ID NO: 1)): L730P, G731V, E732K, G733V, E734K, L760M, K761E, E762K, N763D, A764V, S765N, P766A, S767C, E768K, L779M, I788M, M868R, K869E, L870Q, V871M, H872R, R873P, D874Y, L881R, L895M, S896N, R897C, D898Y, V899G, Y900D, E901K, E902K, D903Y, S904C, Y905D, V906M, K907E, R908P, S909C, Q910R, G911C, and R912P. These mutations (which may also include single or multiple amino acid changes, insertions within or flanking the sequences, and deletions within or flanking the sequences) are thought to induce a steric hindrance and/or an active conformational effect that changes inhibitor binding characteristics.
Compounds of formulas (I), (II), and (III) as described herein may be useful in treating patients that develop cancers with certain RET inhibitor resistance mutations. For example, resistance mutations that result in an increased resistance to a RET inhibitor like a substitution at amino acid position 804 (e.g., V804M, V804L, or V804E), and/or one or more other RET inhibitor resistance mutations like those discussed above may be treated by either dosing in combination or as a follow-up therapy to existing drug treatments. For example, if a patient is treated with a first RET kinase inhibitor and the patient develops a RET inhibitor resistance mutation, the patient could then be subsequently treated with a compound of formulas (I), (II), and (III) as described herein, or pharmaceutically acceptable salts thereof (assuming that the compound of formulas (I), (II), and (III) as described herein is a suitable inhibitor of the particular RET kinase inhibitor mutation present). As another example, if a patient is known to have a particular RET kinase inhibitor mutation (or multiple mutations), the patient could simultaneously be treated with multiple RET kinase inhibitors including a compound (or compounds) of formulas (I), (II), and (III) as described herein, or pharmaceutically acceptable salts thereof that are effective against the RET kinase inhibitor mutation(s) present). Examples of currently known RET kinase inhibitors include alectinib, BLU6864, cabozantinib, dovitinib, foretinib, lenvatinib, ponatinib, pralsetinib, selpercatinib, sorafenib, sunitinib, and vandetanib.
The types of cancers that can be treated using the methods described herein include hematological cancer or solid tumor cancer. Examples of the types of cancer that can be treated using a compound of formulas (I), (II), and (III) as described herein include lung cancer (e.g., small cell lung carcinoma or non-small cell lung carcinoma), thyroid cancer (e.g., papillary thyroid cancer, medullary thyroid cancer, differentiated thyroid cancer, recurrent thyroid cancer, or refractory differentiated thyroid cancer), thyroid adenoma, endocrine gland neoplasms, lung adenocarcinoma, bronchioles lung cell carcinoma, multiple endocrine neoplasia type 2A or 2B (MEN2A or MEN2B, respectively), pheochromocytoma, parathyroid hyperplasia, breast cancer, mammary cancer, mammary carcinoma, mammary neoplasm, colorectal cancer (e.g., metastatic colorectal cancer), papillary renal cell carcinoma, ganglioneuromatosis of the gastroenteric mucosa, inflammatory myofibroblastic tumor, and cervical cancer. Specifically, the types of cancer can be lung cancer or thyroid cancer. More specifically, the cancer can be non-small cell lung carcinoma or medullary thyroid cancer. Further examples of the types of cancers that can be treated using the compounds of formulas (I), (II), and (III) and the methods as described herein include acute lymphoblastic leukemia (ALL), acute myeloid leukemia (AML), cancer in adolescents, adrenocortical carcinoma, anal cancer, appendix cancer, astrocytoma, atypical teratoid/rhabdoid tumor, basal cell carcinoma, bile duct cancer, bladder cancer, bone cancer, brain stem glioma, brain tumor, breast cancer, bronchial tumor, Burkitt lymphoma, carcinoid tumor, unknown primary carcinoma, cardiac tumors, cervical cancer, childhood cancers, chordoma, chronic lymphocytic leukemia (CLL), chronic myelogenous leukemia (CML), chronic myeloproliferative neoplasms, neoplasms by site, neoplasms, colon cancer, colorectal cancer, craniopharyngioma, cutaneous T-cell lymphoma, bile duct cancer, ductal carcinoma in situ, embryonal tumors, endometrial cancer, ependymoma, esophageal cancer, esthesioneuroblastoma, Ewing sarcoma, extracranial germ cell tumor, extragonadal germ cell tumor, extrahepatic bile duct cancer, eye cancer, fallopian tube cancer, fibrous histiocytoma of bone, gallbladder cancer, gastric cancer, gastrointestinal carcinoid tumor, gastrointestinal stromal tumors (GIST), germ cell tumor, gestational trophoblastic disease, glioma, hairy cell tumor, hairy cell leukemia, head and neck cancer, thoracic neoplasms, head and neck neoplasms, CNS tumor, primary CNS tumor, heart cancer, hepatocellular cancer, histiocytosis, Hodgkin's lymphoma, hypopharyngeal cancer, intraocular melanoma, islet cell tumors, pancreatic neuroendocrine tumors, Kaposi sarcoma, kidney cancer, Langerhans cell histiocytosis, laryngeal cancer, leukemia, lip and oral cavity cancer, liver cancer, lung cancer, lymphoma, macroglobulinemia, malignant fibrous histiocytoma of bone, osteocarcinoma, melanoma, Merkel cell carcinoma, mesothelioma, metastatic squamous neck cancer, midline tract carcinoma, mouth cancer, multiple endocrine neoplasia syndromes, multiple myeloma, mycosis fungoides, myelodysplastic syndromes, myelodysplastic/myeloproliferative neoplasms, neoplasms by site, neoplasms, myelogenous leukemia, myeloid leukemia, multiple myeloma, myeloproliferative neoplasms, nasal cavity and paranasal sinus cancer, nasopharyngeal cancer, neuroblastoma, non-Hodgkin's lymphoma, non-small cell lung cancer, lung neoplasm, pulmonary cancer, pulmonary neoplasms, respiratory tract neoplasms, bronchogenic carcinoma, bronchial neoplasms, oral cancer, oral cavity cancer, lip cancer, oropharyngeal cancer, osteosarcoma, ovarian cancer, pancreatic cancer, papillomatosis, paraganglioma, paranasal sinus and nasal cavity cancer, parathyroid cancer, penile cancer, pharyngeal cancer, pheochromocytoma, pituitary cancer, plasma cell neoplasm, pleuropulmonary blastoma, pregnancy and breast cancer, primary central nervous system lymphoma, primary peritoneal cancer, prostate cancer, rectal cancer, colon cancer, colonic neoplasms, renal cell cancer, retinoblastoma, rhabdomyosarcoma, salivary gland cancer, sarcoma, Sezary syndrome, skin cancer, small cell lung cancer, small intestine cancer, soft tissue sarcoma, squamous cell carcinoma, squamous neck cancer, stomach cancer, T-cell lymphoma, testicular cancer, throat cancer, thymoma and thymic carcinoma, thyroid cancer, transitional cell cancer of the renal pelvis and ureter, unknown primary carcinoma, urethral cancer, uterine cancer, uterine sarcoma, vaginal cancer, vulvar cancer, and Wilms' tumor.
Examples of the types of hematological cancers that can be treated using the compounds of formulas (I), (II), and (III) and the methods as described herein include leukemias, lymphomas (non-Hodgkin's lymphoma), Hodgkin's disease (also called Hodgkin's lymphoma), and myeloma, for instance, acute lymphocytic leukemia (ALL), acute myeloid leukemia (AML), acute promyelocytic leukemia (APL), chronic lymphocytic leukemia (CLL), chronic myeloid leukemia (CML), chronic myelomonocytic leukemia (CMML), chronic neutrophilic leukemia (CNL), acute undifferentiated leukemia (AUL), anaplastic large-cell lymphoma (ALCL), prolymphocytic leukemia (PML), juvenile myelomonocyctic leukemia (JMML), adult T-cell ALL, AML with trilineage myelodysplasia (AML/TMDS), mixed lineage leukemia (MLL), myelodysplastic syndromes (MDSs), myeloproliferative disorders (MPD), and multiple myeloma (MM). Additional examples of hematological cancers include myeloproliferative disorders (MPD) such as polycythemia vera (PV), essential thrombocytopenia (ET) and idiopathic primary myelofibrosis (IMF/IPF/PMF). In one embodiment, the hematological cancer (e.g., the hematological cancer that is a RET-associated cancer) is AML or CMML.
Examples of the types of solid tumor cancers that can be treated using the compounds of formulas (I), (II), and (III) and the methods as described herein include thyroid cancer (e.g., papillary thyroid carcinoma, medullary thyroid carcinoma), lung cancer (e.g., lung adenocarcinoma, small-cell lung carcinoma), pancreatic cancer, pancreatic ductal carcinoma, breast cancer, colon cancer, colorectal cancer, prostate cancer, renal cell carcinoma, head and neck tumors, neuroblastoma, and melanoma.
A compound of formulas (I), (II), and (III) as described herein, or pharmaceutically acceptable salts thereof, can be used in the manufacture of a medicament for the treatment of RET-associated diseases or disorders such as IBS or cancer. Cancers that can be treated using such a medicament are described herein above. Use of a compound of formulas (I), (II), or (III) as described herein, or pharmaceutically acceptable salts thereof, in the manufacture of a medicament can also include a step of performing an in vitro assay using a biological sample from a patient, determining the presence of a dysregulation of a RET gene, a RET kinase, or expression or activity or level of any of the same, and administering a therapeutically effective amount of the compound of formulas (I), (II), and (III) as described herein, to the patient if a dysregulation of a RET gene, a RET kinase, or expression or activity or level of any of the same is present. In these uses, the biological sample can be a tumor sample and the tumor sample can be analyzed using methods known to those of skill in the art such as genomic/DNA sequencing. Additionally, in these uses the sample can be obtained from the patient prior to the first administration of the compound of formulas (I), (II), and (III) as described herein. In these uses of the compound of formulas (I), (II), and (III) as described herein in a therapy can be based upon a patient being selected for treatment by having at least one dysregulation of a RET gene, a RET kinase, or expression or activity or level of any of the same. Also, in these uses a compound of formulas (I), (II), and (III), as described herein, or pharmaceutically acceptable salts thereof, may be administered to the patient at a dose of about 1 mg/kg to 200 mg/kg (effective dosage sub-ranges are noted herein above).
The compounds of formulas (I), (II), and (III) as described herein or pharmaceutically acceptable salts thereof, may be prepared by a variety of procedures known in the art, as well as the Preparations and Examples below. The specific synthetic steps for each of the routes described may be combined in different ways, or in conjunction with steps from different schemes, to prepare compounds of formulas (I), (II), and (III) or pharmaceutically acceptable salts thereof. The products of each step in the schemes below can be recovered by conventional methods well known in the art, including extraction, evaporation, precipitation, chromatography, filtration, trituration, and crystallization. The reagents and starting materials are readily available to one of ordinary skill in the art.
Certain stereochemical centers have been left unspecified and certain substituents have been eliminated in the following schemes for the sake of clarity and are not intended to limit the teaching of the schemes in any way. Furthermore, individual isomers, enantiomers, and diastereomers may be separated or resolved by one of ordinary skill in the art at any convenient point in the synthesis of compounds of the invention, by methods such as selective crystallization techniques or chiral chromatography (See for example, J. Jacques, et al., “Enantiomers, Racemates, and Resolutions”, John Wiley and Sons, Inc., 1981, and E. L. Eliel and S. H. Wilen, “Stereochemistry of Organic Compounds”, Wiley-Interscience, 1994). For example, the following molecule has two chiral centers designated by a ϕ(as above in formula (I)ϕ) and an asterisk (*) to show a second chiral center. There are four possible isomers of this molecule that can be isolated without the absolute stereochemistry being determined, i.e., these diastereomer pairs can be RR, RS, SR, and SS. In cases where stereochemistry is not determined, the molecules may be differentiated by their retention time on a chiral column.
For example, the designations “isomer 1” and “isomer 2” refer to the compounds that elute from chiral chromatography first and second, respectively, under the conditions described herein and if chiral chromatography is initiated early in the synthesis, the same designation is applied to subsequent intermediates and examples. Similarly, when diasteromers are also present, the designations “diastereomer A” and “diastereomer B” in addition to the isomer 1 and isomer 2 designations are used. Additionally, the intermediates described in the following schemes may contain a number of nitrogen protecting groups. The variable protecting group may be the same or different in each occurrence depending on the particular reaction conditions and the particular transformations to be performed. The protection and deprotection conditions are well known to the skilled artisan and are described in the literature (See for example “Greene's Protective Groups in Organic Synthesis”, Fourth Edition, by Peter G. M. Wuts and Theodora W. Greene, John Wiley and Sons, Inc. 2007).
Certain abbreviations are defined as follows: “ACN” refers to acetonitrile; “ATP” refers to adenosine triphosphate; “BSA” refers to Bovine Serum Albumin; “n-BuLi” refers to n-butyl lithium; “DCM” refers to dichloromethane or methylene chloride; “DEA” refers to diethylamine; “DIPEA” refers to N,N-diisopropylethylamine or N-ethyl-N-isopropyl-propan-2-amine; “DMA” refers to dimethylamine; “DMF” refers to N,N-dimethylformamide; “DMSO” refers to dimethyl sulfoxide; “DTT” refers to dithiothreitol; “Et3N” refers to triethylamine; “EtOAc” refers to ethyl acetate; “ee” refers to enantiomeric excess; “Et2O” refers to diethyl ether; “EtOH” refers to ethanol or ethyl alcohol; “FA” refers to formic acid; “GST” refers to glutathione S-transferase; “HEK” refers to human embryonic kidney; “hr” or “hrs” refers to hour or hours; “HTRF” refers to homogeneous time resolved fluorescence; “IgG” refers to immunoglobulin G; “IPA” refers to isopropyl alcohol or isopropanol; “KOAc” refers to potassium acetate; “LDA” refers to lithium diisopropylamide; “MeOH” refers to methanol or methyl alcohol; “MeTHF” refers to 2-methyltetrahydrofuran; “min” refers to minute or minutes; “Mn(dpm)3” refers to manganese(3+) tris[(3Z)-2,2,6,6-tetramethyl-5-oxo-3-hepten-3-olate]; “MtBE” refers to methyl tert-butyl ether; “NaOAc” refers to sodium acetate; “NBS” refers to N-bromosuccinimide; “NMI” refers to 1-methylimidazole or N-methylimidazole; “PBS-T” refers to Phosphate Buffered Saline+Tween®20; “Pd(dppf)Cl2)” refers to [1,1′ bis(diphenylphosphino)ferrocene]dichloropalladium (II); “PE” refers to petroleum ether; “PhSiH3” refers to phenylsilane; “RT” refers to room temperature; “TCHF” refers to tetramethylchloroformamidinium hexafluorophosphate; “tert-BuOH” refers to tert butyl alcohol; “TCFH” refers to N,N,N′,N′-tetramethylchloroformamidinium hexafluorophosphate; “TFA” refers to trifluoroacetic acid; “THF” refers to tetrahydrofuran; and “T3P®” refers to propanephosphonic acid anhydride, 2,4,6-tripropyl-1,3,5,2,4,6-trioxatriphosphorinane-2,4,6-trioxide, or PPACA; “t(R)” refers to retention time and “WT” refers to wild-type.
In the schemes below, all substituents unless otherwise indicated, are as previously defined. The reagents and starting materials are generally readily available to one of ordinary skill in the art. Others may be made by standard techniques of organic and heterocyclic chemistry which are analogous to the syntheses of known structurally similar compounds and the procedures described in the Preparations and Examples which follow including any novel procedures. Intermediates and processes useful for the synthesis of the compounds described by formula (I) are intended to be included in this description.
Scheme 1 depicts the preparation of the compounds of (13), which can be used to prepare the compounds of formulas (I), (II), and (III). A person of ordinary skill in the art will recognize that aryl aldehyde (1) may undergo condensation with alkyl hydrazine (4) to furnish hydrazone (2). Hydrazone (2) may be halogenated by employing reagents well known in the art to provide hydrazonoyl bromide (3). Amino pyrazole (6) may be formed via condensation of hydrazonoyl bromide (3) with malononitrile and an ensuing annulation. Amino pyrazole (6) may also be synthesized by reacting the appropriately substituted hydrazine (4) with the appropriate dinitrile Michael acceptor (5). Borylation of aryl bromide (6) under typical Miyaura reaction conditions may provide boronic ester (7). Treatment of boronic ester (7) with the appropriate metal catalyst and halide may afford α,β unsaturated ester (8). Reduction of olefin (8) may be achieved under reductive conditions such as a hydrogen atmosphere and suitable metal catalyst, preferably Pd/C, to furnish the α-methyl ester (13).
Scheme 2 depicts the preparation of the compounds of formulas (I), (II), and (III), as described herein. The skilled artisan will recognize that an alternative synthesis of α-methyl ester (13) may be achieved by α-methylation of methyl acetate (9) under archetypal enolate alkylation conditions to provide a methyl ester (10). Borylation via Miyaura conditions of the aryl bromide (10) may furnish boronate (11) in essentially the same manner as described for the boranate (7) in Scheme 1. Treatment of boronate ester (11) with the appropriate bromopyrazole (12) and metal catalyst, under Suzuki coupling conditions may afford α-methyl ester (13). Carboxylic acid (14) may be obtained by saponification of ester (13) with the proper nucleophilic base. The enantiomers of the carboxylic acid (14) may be separated using chiral separation techniques well known in the art or separated at a later step in the synthesis. Carboxylic acid (14) and primary amine (15) may be joined by utilizing the appropriate amide coupling reagent under conditions suitable for amide bond formation to provide (16). The nitrile moiety of amino pyrazole (16) may be converted to compounds of formulas (I), (II), and (III), as described herein, under a variety of conditions such as metal catalyzed hydration, acidic hydrolysis, and oxidation. The enantiomers may be separated using chiral separation techniques well known in the art to give the compounds of formulas (I), (II), and (III), as described herein.
To methyl 2-(5-bromopyridin-2-yl)acetate (4.20 g, 17.5 mmol) in THF (84 mL) under N2 and at −20° C. is added 60% NaH (w/w) in mineral oil (771 mg, 19.3 mmol). The mixture is stirred at −20° C. until gas evolution has subsided. To the reaction mixture is then added iodomethane (4.4 mL, 70.1 mmol). The mixture is stirred for 5 min at −20° C. after which time it is allowed to warm to RT. After 1 hr the reaction mixture is concentrated under reduced pressure and dried under vacuum. To the residue is added DCM (15 mL), H2O (10 mL) and saturated aqueous NaHCO3 solution (10 mL). The organic layer is separated, dried over Na2SO4, filtered, and concentrated under reduced pressure. The crude material is purified by silica gel flash chromatography eluting with a gradient of EtOAc in DCM from 0% to 20% to give the title compound as a colorless oil (3.16 g, 68.59%).
60% NaH (w/w) in mineral oil (3.85 g, 96.091 mmol) is added to THF (180 mL) in portions at RT under N2. To this mixture is added malononitrile (3.17 g, 48.046 mmol) in THF (20 mL) dropwise at 0-10° C. and the mixture is stirred for 30 min at RT. To this mixture is added methyl 2-(4-chlorocarbonylphenyl)propanoate (13 g, crude) in THF (30 mL) dropwise at 0° C. and the mixture is stirred for 2 hrs at RT. The resulting mixture is used directly without further purification.
To a stirred mixture of NaH (1.68 g, 42.13 mmol, 60%) in THF (100 mL) is added malononitrile (1.53 g, 23.160 mmol) in THF (100 mL) dropwise at 0° C. under N2. The mixture is stirred for 30 min at RT under N2. To the above mixture is added 4-bromo-2,3-difluorobenzoyl chloride in THF (10 mL) dropwise at 0° C. The mixture is stirred for additional 2 hr at RT. The mixture is used without further purification.
To crude methyl 2-[4-(2,2-dicyano-1-hydroxy-vinyl)phenyl]propanoate in THF solution is added dimethyl sulfate (7.67 g, 60.810 mmol) dropwise at RT under N2 and the mixture is stirred overnight at 80° C. under N2. The mixture is allowed to cool to RT and quenched with H2O (300 mL). The mixture is extracted with EtOAc (3×300 mL) and the combined organic extracts are washed with saturated aqueous NaCl solution (3×500 mL), dried over anhydrous Na2SO4, filtered, and concentrated under reduced pressure. The residue is purified by silica gel column chromatography, eluting with hexanes/EtOAc (6:1-1:1) to give the title compound (5 g, 36.49% over 3 steps) as a yellow oil. 1H NMR (d6-DMSO) δ 7.71-7.62 (m, 2H), 7.59-7.50 (m, 2H), 4.00-3.93 (m, 1H), 3.90 (s, 3H), 3.63 (s, 3H), 1.44 (d, 3H).
To crude 2-[(4-bromo-2,3-difluoro-phenyl)-hydroxy-methylene]propanedinitrile is added dimethyl sulfate (3.35 g, 26.56 mmol) dropwise at RT. The mixture is stirred overnight at 80° C. under N2. The mixture is cooled to RT. The reaction is quenched with H2O at RT. The mixture is extracted with EtOAc (3×100 mL). The combined organic extracts are washed with brine (3×100 mL), dried over anhydrous Na2SO4, filtered and the filtrate is concentrated under reduced pressure. The residue is purified by silica gel column chromatography, eluting with PE/EtOAc (3:1-2:1) to give the title compound (5.0 g, 75.5% over 3 steps) as a light grey solid. 1H NMR (300 MHz, CDCl3) δ7.64-7.54 (m, 1H), 7.18-7.11 (m, 1H), 3.99 (d, 3H).
Into a solution of 2-(4-bromo-2-fluorobenzoyl)propanedinitrile (23.40 g, 87.62 mmol) in THF (300 mL), is added dimethyl sulfate (13.26 g, 105.13 mmol) and the mixture is stirred overnight at 80° C. under N2. The solution is cooled to RT and concentrated under reduced pressure. The crude product is dissolved in EtOAc (200 mL) and diluted with H2O (200 mL). The mixture is extracted with EtOAc (3×200 mL) and the organic extract is washed with brine (2×100 mL), dried over anhydrous Na2SO4, and concentrated under reduced pressure. The crude product is purified by silica gel chromatography eluting with a gradient of 5:1 to 3:1 PE to EtOAc to give the title product (23.5 g, 95.4%) as brown semi-solid. ES/MS m/z (79Br/81Br) 265.0/267.0 [M+H]+.
To a stirred mixture of LDA (20.81 mL, 41.62 mmol) in THF (100 mL) is added ACN (1.82 g, 44.33 mmol) in THF dropwise at −70° C. The mixture is stirred for 30 min at −70° C. To the above mixture is added ethyl 3,3-difluoro-2,2-dimethylbutanoate (5 g, 27.75 mmol) in THF dropwise at −70° C. and the mixture is slowly warmed to RT. The reaction is quenched by the addition of sat. NH4Cl (aq.) (30 mL) at 0° C. and extracted with PE (200 mL). The aqueous phase is acidified to pH=3 with HCl (aq.) (1 N) and extracted with EtOAc (3×100 mL). The EtOAc extracts are washed with saturated aqueous NaCl solution (3×50 mL), dried over anhydrous Na2SO4, filtered, and the filtrate is concentrated under reduced pressure to give the title compound (1.9 g, 39.09%) as a brown oil which is used without further purification. 1H NMR (CDCl3) δ3.79 (s, 2H), 1.63 (t, 3H), 1.34 (s, 6H).
60% NaH (w/w) in mineral oil (140 mg, 3.5 mmol) in THF (1 mL) is added dropwise to a stirring solution of benzyl 2-(3-bicyclo[1.1.1]pentanyl)acetate (504 mg, 2.33 mmol) and ACN (134 μL, 2.56 mmol) in THF (8 mL, 0.3 M) at RT. The reaction mixture is heated and stirred at 60° C. for 25 min. The reaction mixture is quenched with ice H2O (10 mL), acidified to pH 5 with HCl (c) and extracted with EtOAc (3×10 mL). The combined organic extracts are washed with saturated aqueous NaCl solution (10 mL), dried over anhydrous Na2SO4, and concentrated under reduced pressure to give the title compound (350 mg).
To THF (5.00 mL) is added n-BuLi (1.71 mL, 4.28 mmol, 2.5 M in THF) at 0° C. under N2. To the mixture is added ACN (187.42 mg, 4.56 mmol) in THF (5 mL) dropwise over 5 min at −78° C. under N2. The mixture is stirred for 1 hr at −78° C. To the mixture is added methyl 3-methylbicyclo[1.1.1]pentane-1-carboxylate (400.00 mg, 2.85 mmol) in THF (5 mL) dropwise at −78° C. under N2. The mixture is stirred for 1 hr at RT. The reaction is quenched by the addition of saturated NH4Cl aq. (20 mL) at 0° C. The mixture is acidified to pH 4 with HCl (1 N) aq. and extracted with DCM (3×50 mL). The combined organic extracts are washed with brine (2×100 mL), dried over anhydrous Na2SO4, filtered and concentrated under reduced pressure, to give the title compound (360 mg, 84.5%) as a brown liquid.
n-BuLi (0.83 mL, 2.087 mmol, 2.5 M in hexanes) is added to THF (10 mL) at 0° C. under N2. ACN (91.34 mg, 2.23 mmol) in THF (2 mL) is added dropwise over 2 min at −78° C. under N2 and the reaction is stirred for 1 hr at −78° C. Methyl 3-(trifluoromethyl)bicyclo[1.1.1]pentane-1-carboxylate (270.00 mg, 1.39 mmol) in THF (2 mL) is added dropwise to the reaction mixture at −78° C. and the reaction is stirred at RT for 12 hr. The reaction is quenched by the addition of sat. NH4Cl (aq., 20 mL), acidified to pH=4 with concentrated HCl, and extracted with DCM (3×50 mL). The combined organic extracts are washed with brine, dried over anhydrous Na2SO4, filtered, and concentrated under reduced pressure. The crude product (290 mg) is used without further purification. 1H NMR (300 MHz, CDCl3) δ3.54 (s, 2H), 2.39 (s, 6H).
The following compound in Table 1 is prepared essentially as described for 3-oxo-3-[3-(trifluoromethyl)bicyclo[1.1.1]pentan-1-yl]propanenitrile, adjusting reaction time to determine completion of the reaction, and purification conditions as appropriate. The reaction can be allowed to warm to RT after the carboxylate is added. n-BuLi can be added in hexanes or THF.
To a stirred solution of Mn(dpm)3 (60.31 mg, 0.100 mmol) in IPA (20.00 mL) is added 3-methoxy-2-methyl-prop-1-ene (860.00 mg, 9.984 mmol), PhSiH3 (1.08 g, 9.984 mmol), and (E)-N-[(tert-butoxycarbonyl)imino](tert-butoxy)formamide (3.45 g, 14.98 mmol) in portions at 0° C. under N2. The resulting mixture is stirred for 2 hrs at RT under N2 and concentrated under vacuum. H2O (15 mL) is added, and the resulting mixture is extracted with EtOAc (3×30 mL). The combined organic extracts are washed with saturated aqueous NaCl solution (2×20 mL), dried over anhydrous Na2SO4, filtered, and concentrated under reduced pressure. The residue is purified by silica gel column chromatography, eluting with a gradient of PE/EtOAc (10:1 to 7:3) to give the title compound (1.8 g, 56.62%) as a colorless oil. 1H NMR (CDCl3) δ3.38-3.32 (m, 5H), 1.49-1.46 (m, 24H).
To a stirred solution of tert-butyl N-(1-methylcyclopropyl)carbamate (2.00 g, 11.68 mmol) in DCM (20.00 mL) is added tert-butyl nitrite (2.40 g, 23.36 mmol) in portions at RT under N2 and the mixture is stirred for 2 hrs at RT under N2. The mixture is concentrated under reduced pressure and the residue is purified by silica gel column chromatography, eluting with PE/EtOAc (25/1 to 20/1) to give the title compound (1.3 g, 55.59%) as a brown liquid. 1H NMR (d6-DMSO) δ1.59 (s, 9H), 1.10 (s, 3H), 0.86-0.84 (m, 2H), 0.70-0.65 (m, 2H).
To a stirred solution of tert-butyl N-(1-methylcyclopropyl)-N-nitroso-carbamate (1.20 g, 5.99 mmol) in 4 N HCl (8.00 mL) is added Zn (783.98 mg, 11.99 mmol) in portions at 0° C. under N2 and the mixture is stirred for 12 hrs at RT under N2. The mixture is filtered, the filter cake is washed with H2O (3×10 mL), and the filtrate is concentrated under reduced pressure to give the title compound (2 g, crude) as an off-white solid which is used directly without further purification. 1H NMR (d6-DMSO) δ1.30 (s, 3H), 0.77-0.73 (m, 2H), 0.54-0.50 (m, 2H).
A solution of tert-butyl N-(tert-butoxycarbonylamino)-N-(2-methoxy-1,1-dimethyl-ethyl)carbamate (1.6 g, 5.00 mmol) in HCl (gas) in 1,4-dioxane (15.00 mL) is stirred for 6 hrs at RT under N2. The mixture is concentrated under vacuum and triturated with Et2O (3×10 mL) to give the title compound (400 mg, 52%) as a semi-solid. 1H NMR (d6-DMSO) δ3.36 (s, 2H), 3.32 (s, 3H), 1.17 (s, 6H).
To a stirred mixture of N′-(1,1,1-trifluoro-2-methylpropan-2-yl)benzohydrazide (7.50 g) in H2O (40.00 mL) is added HCl (c) (40.00 mL) in portions at RT under N2. The resulting mixture is stirred for 12 hrs at 80° C. under N2. The mixture is allowed to cool to RT and concentrated under reduced pressure. The resulting solid is triturated with Et2O (30 mL) and the precipitated solids are collected by filtration and washed with Et2O (3×30 mL) to give the title compound (4.0 g, 61%) as an off-white solid. 1H NMR (d6-DMSO) δ9.55 (br, s, 2H), 5.60 (br, s, 3H), 1.34 (s, 6H).
A solution of 4-bromo-benzaldehyde (100.00 g, 540.48 mmol), isopropylhydrazine hydrochloride (65.75 g, 594.53 mmol), and DIPEA (76.84 g, 594.53 mmol) in DMF (500 mL) is stirred for 3 hrs at 80° C. under N2. The reaction is cooled to RT. The resulting mixture is used directly without workup or further purification. ES/MS m/z (79Br/81Br) 241.1/243.1 [M+H]+.
The following compounds in Table 1a are prepared essentially as described for N-[(E)-(4-bromophenyl)methyleneamino]propan-2-amine using the appropriate reagents and adjusting reaction times to determine completion of the reactions.
To a crude solution of 1-bromo-1,1-difluoro-propan-2-one (200 mL of 3/1 Et2O/toluene) is added benzohydrazide (23.62 g) in sealed tube at RT under N2. The mixture is stirred 2 hrs at 50° C. under N2. The mixture is allowed to cool to RT. The precipitated solids are collected by filtration and washed with toluene (3×100 mL) to give the title compound (28 g, 34%, over 2 steps, purity 62% on 1H-NMR) as a white solid.
To a stirred mixture of 1,1,1-trideuteriopropan-2-one (0.24 g, 3.93 mmol) in THF (50 mL) is added benzohydrazide (2.14 g, 15.71 mmol, dissolved in THF (10 mL)) dropwise at −78° C. under N2. The mixture is stirred for 2 hrs at −78° C. The mixture is diluted with EtOAc (200 mL). The organic phase is washed with H2O (2×50 mL) and brine (50 mL), dried over anhydrous Na2SO4, filtered, and the filtrate is concentrated under reduced pressure to give the title compound which is used directly without further purification. ES/MS (m/z) 180.1 (M+H).
To a stirred solution of benzohydrazide (5.00 g, 36.723 mmol) in MeOH (100.00 mL) is added 1,1,1,3,3,3-hexadeuteriopropan-2-one (2.35 g, 36.723 mmol) dropwise at RT. The mixture is stirred overnight at RT and then concentrated under reduced pressure to give the title compound (5 g, 74.70%) as a white solid. ES/MS (m/z) 183.3 (M+H).
To a stirred mixture of (Z/E)-N-[(2,2,2-trideuterio-1-methyl-ethylidene)amino]benzamide (695 mg, 3.88 mmol) in MeOH (5 mL) is added NaBH4 (293.40 mg, 7.76 mmol) in portions at 0° C. The mixture is stirred at rt for 1 hr. The mixture is diluted with EtOAc (100 mL), washed with H2O (30 mL), brine (30 mL), dried over anhydrous Na2SO4, filtered, and concentrated under reduced pressure. The residue is purified by silica gel column chromatography, eluting with PE:EtOAc (3:1˜1:3) to give the title compound (280 mg, 39.8%) as a white solid. ES/MS (m/z) 182.2 (M+H).
To a stirred solution of N-[[2,2,2-Trideuterio-1-(trideuteriomethyl)ethylidene]amino]benzamide (2.00 g, 10.97 mmol) in MeOH (30.00 mL) is added NaBH4 (0.81 g, 21.95 mmol) in portions at RT. The mixture is stirred for 2 hrs. The reaction is quenched with H2O (50 mL) and extracted with DCM (3×50 mL). The combined organic extracts are washed with H2O (3×50 mL), dried over anhydrous Na2SO4, and concentrated under reduced pressure to give the title compound (1.9 g, 93.96%) as a white solid. ES/MS (m/z) 185.3 (M+H).
To a stirred mixture of (Z/E)-N-[(2,2,2-trideuterio-1-methyl-ethylidene)amino]benzamide (695.00 mg, 3.88 mmol) in CD3OD (5 mL) is added NaBD4 (326.15 mg, 7.77 mmol) in portions at 0° C. The mixture is stirred at RT for 1 hr. The mixture is diluted with EtOAc (100 mL) and washed with H2O (30 mL) brine (30 mL), dried over anhydrous Na2SO4, filtered, and the filtrate is concentrated under reduced pressure. The residue is purified by silica gel chromatography eluting with PE:EtOAc (3:1˜1:3) to give the title compound (260 mg, 36.6%) as a white solid. ES/MS (m/z) 183.2 (M+H).
The following compound in Table 1b is prepared essentially as described for N′-(1,2,2,2-tetradeuterio-1-methyl-ethyl)benzohydrazide using the appropriate reagents and adjusting reaction times to determine completion of the reactions. NaBD4 can be added at RT and can be used without further purification.
To a stirred solution of N′-[(2E)-1-bromo-1,1-difluoropropan-2-ylidene]benzohydrazide (12 g, 41.22 mmol) in THF (100 mL) is added BH3-THF (82.45 mL, 82.45 mmol, 1 M in THF) dropwise at 0° C. under N2. The mixture is stirred for 12 hrs at RT under N2. The reaction is quenched by the addition of MeOH (5 mL) at 0° C. The mixture is diluted with H2O (50 mL) and extracted with DCM (3×50 mL). The combined organic extracts are washed with brine (2×100 mL), dried over anhydrous Na2SO4, filtered, and concentrated under reduced pressure. The residue is purified by silica gel column chromatography, eluting with PE/EtOAc (8/1 to 6/1) to give the title compound (7 g, 57%) as a white solid. 1H NMR (400 MHz, CDCl3) δ 7.78-7.73 (m, 2H), 7.60-7.53 (m, 1H), 7.52-7.45 (m, 2H), 3.57-3.49 (m, 1H), 1.45 (d, 3H).
A mixture of N′-[2,2,2-trideuterio-1-(trideuteriomethyl)ethyl]benzohydrazide (500 mg, 2.71 mmol) in HCl (5.00 mL, cone) is stirred overnight at 80° C. The mixture is allowed to cool to RT and concentrated under reduced pressure. The crude product is triturated with Et2O (3 mL). The resulting precipitate is filtered, and the filter cake is washed with Et2O (3×2 mL) to give the title compound (180 mg, 56.88%) as a white solid.
The following compounds in Table 1c are prepared essentially as described for [2,2,2-trideuterio-1-(trideuteriomethyl)ethyl]hydrazine.HCl using the appropriate reagents and adjusting reaction times to determine completion of the reactions.
To N-[(E)-(4-bromophenyl)methyleneamino]propan-2-amine is added NBS (106.04 g, 595.77 mmol) in DMF dropwise and the mixture is stirred for 3 hrs at 0° C. under N2. The resulting mixture is used directly without workup or further purification.
The following compounds in Table 2 are prepared essentially as described for (1Z)-4-bromo-N-isopropyl-benzohydrazonoyl bromide using the appropriate reagents and adjusting reaction times to determine completion of the reactions.
A solution of sodium ethoxide (91.88 g, 1.351 mol) and propanedinitrile (39.24 g, 594.53 mmol) in EtOH (400 mL) is stirred for 1 hr at 0° C. under N2. The crude solution of (1Z)-4-bromo-N-isopropyl-benzohydrazonoyl bromide is added to the mixture. The mixture is stirred for 2 hrs at RT. The mixture is concentrated under reduced pressure, diluted with H2O (3 L), and the resulting precipitated solids are collected by filtration, washed with H2O (3×200 mL), and the solid is dried in an oven at 50° C. to give the title compound (127 g, 73.7% over 3 steps). ES/MS (m/z) (79Br/81Br 305/307 (M+H).
The following compounds in Table 3 are prepared essentially as described for 5-amino-3-(4-bromophenyl)-1-isopropylpyrazole-4-carbonitrile using the appropriate reagents, adjusting reaction times to determine completion of the reactions and purification conditions if appropriate. The crude reaction can be diluted with H2O, extracted with EtOAc, and purified with chromatography using appropriate conditions.
(1-Methylcyclopropyl)hydrazine hydrochloride (1.63 g, 13.30 mmol), THF (20 mL), Et3N (3.08 g, 30.41 mmol), and 2-[(4-bromophenyl)(methoxy)methylidene]propanedinitrile (1.00 g, 3.80 mmol) are added together and stirred for 6 hrs at 50° C. The resulting mixture is diluted with EtOAc (100 mL), washed with H2O (2×30 mL), and saturated aqueous NaCl solution (20 mL). The organic phase is concentrated under reduced pressure. The residue is purified by reverse Combi-flash chromatography with the following conditions: C18; ACN in H2O (0.1% NH4HCO3), UV 254 nm eluting with a gradient of 70% to 100% in 15 mins to give the title compound (375 mg, 31%) as an off-white solid. ES/MS m/z (79Br/81Br) 317.0/319.0 [M+H]+.
The following compounds in Table 3a are prepared essentially as described for 5-amino-3-(4-bromophenyl)-1-(1-methylcyclopropyl)pyrazole-4-carbonitrile using the appropriate reagents, adjusting reaction times to determine completion of the reactions. The Et3N can be added dropwise. The crude reaction can be concentrated to dryness and purified as appropriate.
A solution of 2-[(4-bromo-2-fluorophenyl)(methoxy)methylidene]propanedinitrile (1.50 g, 5.34 mmol), (1-methylcyclopropyl)hydrazine HCl (1.96 g, 15.99 mmol) and Et3N (2.70 g, 26.682 mmol) in EtOH (20.00 mL) is stirred for 1 hr at RT under N2. The mixture is concentrated under reduced pressure and the residue is purified by silica gel chromatography, eluting with a gradient of 3:1 to 2:1 PE:EtOAc to give the title compound (1.2 g, 67.09%) as a light yellow solid. ES/MS m/z (79Br/81Br) 335.1/337.1 [M+H]+.
The following compounds in Table 3b are prepared essentially as described for 5-amino-3-(4-bromo-2-fluorophenyl)-1-(1-methylcyclopropyl)pyrazole-4-carbonitrile using the appropriate reagents, adjusting reaction times to determine completion of the reactions and purification conditions if appropriate. The reaction can be stirred at 50° C. and the hydrazine can be the free amine if available.
To a stirred solution of 5-amino-1-(1-bromo-1,1-difluoropropan-2-yl)-3-(4-bromophenyl)pyrazole-4-carbonitrile (300.00 mg, 0.71 mmol, co-evaporated with 2×CD3OD) in CD3COOD (3.00 mL) is added Zn (467.14 mg, 7.14 mmol, co-evaporated with 2×CD3OD) in portions at RT under N2. The mixture is stirred for 1 hr at 80° C. under N2. The mixture is allowed to cool to RT and quenched with EtOAc. The mixture is filtered, the filter cake is washed with EtOAc (3×10 mL) and concentrated under reduced pressure. The residue is purified by silica gel column chromatography, eluting with PE/EtOAc (2:1-1:1) to give the title compound (100 mg, 40.92%) as a yellow solid. 1H NMR (300 MHz, d6-DMSO) δ7.79-7.65 (m, 4H), 7.00 (s, 2H), 4.93-4.68 (m, 1H), 1.48 (d, 3H).
A solution of methyl 2-[4-(2,2-dicyano-1-methoxyeth-1-en-1-yl)phenyl]propanoate (500 mg, 1.85 mmol), [2,2,2-trideuterio-1-(trideuteriomethyl)ethyl]hydrazine.HCl (648 mg, 5.56 mmol) and Et3N (936 mg, 9.25 mmol) in EtOH (20 mL) is stirred for 1 hr at RT. The solution is diluted with H2O (30 mL) and extracted with EtOAc (3×50 mL). The organic layer is dried over anhydrous Na2SO4 and concentrated under reduced pressure to give the title compound (650 mg, crude) as a light yellow solid. The crude product is used without further purification. ES/MS (m/z) 319.40 (M+H).
To a stirred solution of 5-amino-1-isopropyl-pyrazole-4-carbonitrile (13.58 g, 85.0 mmol) in THF (170 mL) are added successively N,N-dimethylpyridin-4-amine (1.05 g, 8.50 mmol), Et3N (36 mL, 0.255 mol), and tert-butoxycarbonyl tert-butyl carbonate (40.81 g, 0.187 mol). The reaction mixture is stirred at RT overnight. The reaction mixture is quenched with a saturated aqueous solution of NH4Cl (15 mL). The aqueous layer is extracted with EtOAc (3×20 mL) and the combined organic extracts are washed with saturated aqueous NaCl solution, dried over Na2SO4, filtered, and concentrated under reduced pressure. The crude is purified by silica gel flash chromatography eluting with a gradient of EtOAc in cyclohexane from 2% to 30% to give the title compound as a pale yellow solid (9.29 g, 31%) and a second batch as a pale yellow solid (4.86 g, 16%) which combined gives 14.15 g, 47% yield.
and
tert-Butyl N-tert-butoxycarbonyl-N-(4-cyano-2-isopropyl-pyrazol-3-yl)carbamate (4.02 g, 11.5 mmol), 4,4,5,5-tetramethyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,3,2-dioxaborolane (2.39 g, 9.42 mmol), di-μ-methoxybis(1,5-cyclooctadiene)diiridium (CAS #12148-71-9) (1:2) (136 mg, 0.21 mmol) and 4-tert-butyl-2-(4-tert-butyl-2-pyridyl)pyridine (112 mg, 0.41 mmol) are added together under vacuum, THF (11.60 mL) is added, and the reaction is kept under N2. The mixture is stirred and heated at 80° C. for 6 hrs. The reaction mixture is cooled to RT and stirred overnight. The reaction mixture is concentrated under reduced pressure and the residue is dissolved in a mixture of DCM/EtOAc 3:1 (10 mL) and this solution is passed through a pad of silica gel and washed with DCM/EtOAc 3:1 (2×10 mL). The filtrates are combined, concentrated under reduced pressure, and dried under vacuum to give a crude residue. To the crude material is added Cs2CO3 (8049 mg, 24.6 mmol), methyl 2-(5-bromo-2-pyridyl)propanoate (2.00 g, 8.19 mmol), Pd(dppf)Cl2) DCM (342 mg, 0.410 mmol) and 4 Å molecular sieves (5 g). The reaction mixture is then degassed by vacuum/N2 (3×) and heated to 100° C. for 2 hrs. The reaction is cooled to RT, filtered through a bed of Perlite and the bed of Perlite being washed with THF (3×60 mL). The organic solutions are combined, concentrated under reduced pressure, and dried under vacuum. To the residue is added DCM (60 mL), H2O (80 mL) and saturated aqueous NaHCO3 solution (60 mL). The organic layer is separated, dried over anhydrous Na2SO4, concentrated under reduced pressure, and dried under vacuum. The crude material is purified by silica gel flash chromatography eluting with a gradient of EtOAc in DCM from 0% to 20% to give the Preparation 22 title compound (2.47 g, 68.53%) and Preparation 23 title compound. The material of Preparation 23 is further purified with silica gel chromatography eluting with a gradient of 10% to 80% EtOAc in cyclohexane to give the title compound of Preparation 23.
A mixture of 5-amino-3-(4-bromophenyl)-1-isopropylpyrazole-4-carbonitrile (100 g, 327.68 mmol), bis(pinacolato)diboron (91.53 g, 360.444 mmol), KOAc (48.24 g, 491.52 mmol), and Pd(dppf)Cl2 (11.99 g, 16.38 mmol) in 1,4-dioxane (1 L) is stirred for 6 hrs at 80° C. under N2. The mixture is allowed to cool to RT. The resulting mixture is filtered, washed with EtOAc (3×100 mL), and concentrated under reduced pressure. The residue is purified by silica gel column chromatography, eluting with PE/EtOAc (10:1-5:1) to give the title compound (100 g, 86.6%) as a brown solid. ES/MS (m/z) 353.2 (M+H).
The following compounds in Table 4 are prepared essentially as described for 5-amino-1-isopropyl-3-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]pyrazole-4-carbonitrile using the appropriate reagents, adjusting reaction times to determine completion of the reactions, and adjusting purification conditions if appropriate. The material can also be filtered without work-up and used without further purification.
5-Amino-3-(4-bromophenyl)-1-(1-methylcyclopropyl)pyrazole-4-carbonitrile (350 mg, 1.10 mmol), bis(pinacolato)diboron (560.41 mg, 2.21 mmol), KOAc (325 mg, 3.31 mmol), and Pd(dppf)Cl2 (121 mg, 0.17 mmol) are added together in dioxane (5.00 mL). The solution is stirred for 2 hrs at 80° C. under N2. The mixture is filtered and used directly without purification. ES/MS (m/z) 365.2 (M+H).
A solution of 5-amino-3-(4-bromo-2-fluorophenyl)-1-(1-methylcyclopropyl)pyrazole-4-carbonitrile (700 mg, 2.09 mmol), 4,4,5,5-tetramethyl-2-(tetramethyl-1,3,2-dioxaborolan-2-yl)-1,3,2-dioxaborolane (636.40 mg, 2.51 mmol), Pd(dppf)Cl2·CH2Cl2 (341.10 mg, 0.42 mmol) and KOAc (614.89 mg, 6.26 mmol) in dioxane (10.00 mL) is stirred for 1 hr at 80° C. under N2. The solution is cooled to RT, filtered, and the filter cake is washed with 1,4-dioxane (2×3 mL). The mixture is used directly without further purification. ES/MS (m/z) 383.3 (M+H).
A solution of 5-amino-3-[2-fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-1-(1-methylcyclopropyl)pyrazole-4-carbonitrile (980 mg, 2.56 mmol), methyl 2-(trifluoromethanesulfonyloxy)prop-2-enoate (1200.61 mg, 5.13 mmol), Pd(dppf)Cl2·CH2Cl2 (418.73 mg, 0.51 mmol) and K2CO3 (708.65 mg, 5.128 mmol) in dioxane/H2O (4:1, 10 mL) is stirred for 1 hr at 80° C. under N2. The solution is cooled to RT and concentrated to dryness under reduced pressure. The residue is purified by silica gel chromatography, eluting with a gradient of 3:1 to 2:1 PE:EtOAc to give the title compound (430 mg, 49.28%) as a yellow solid. ES/MS (m/z) 341.2 (M+H).
A mixture of 5-amino-1-isopropyl-3-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]pyrazole-4-carbonitrile (100.00 g, 283.89 mmol), methyl 2-(trifluoromethanesulfonyloxy)prop-2-enoate (99.71 g, 425.83 mmol), K2CO3 (117.71 g, 851.67 mmol) and Pd(dppf)Cl2 (10.39 g, 14.19 mmol) in 1,4-dioxane (1 L) and H2O (250 mL) is stirred overnight at 90° C. under N2. The mixture is allowed to cool to RT. The resulting mixture is filtered, and the filter cake is washed with EtOAc (3×100 mL). The filtrate is concentrated under reduced pressure, diluted with H2O (500 mL), and extracted with EtOAc (3×500 mL). The combined organic extracts are washed with saturated aqueous NaCl solution (3×200 mL), dried over anhydrous Na2SO4, filtered, and concentrated under reduced pressure. The residue is purified by silica gel column chromatography, eluting with PE/EtOAc (10:1-3:1) to give the title compound (43 g, 48.8%) as a yellow solid. ES/MS (m/z): 311.2 (M+H).
The following compounds in Table 5 are prepared essentially as described for methyl 2-[4-(5-amino-4-cyano-1-isopropyl-pyrazol-3-yl)phenyl]prop-2-enoate using the appropriate reagents and adjusting reaction times to determine completion of the reactions. Temperature is varied from 80-90° C. and dioxane and H2O can be used as solvents.
5-Amino-1-(1-methylcyclopropyl)-3-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]pyrazole-4-carbonitrile (400 mg, 1.10 mmol), methyl 2-(trifluoromethanesulfonyloxy)prop-2-enoate (642.95 mg, 2.7 5 mmol), K2CO3 (455 mg, 3.30 mmol), and Pd(dppf)Cl2 (85 mg, 0.09 mmol) are added together in dioxane (6.00 mL) and H2O (1.50 mL). The solution is stirred for 2 hrs at 80° C. The mixture is diluted with EtOAc (100 mL), washed with H2O (2×30 mL), and brine (20 mL). The organic phase is separation and concentrated under reduced pressure. The residue is purified by reversed combi-chromatography with following conditions: C18; eluting with a gradient of ACN in H2O (0.1% NH4HCO3) to give the title compound (280 mg, 78.5) as a brown solid. ES/MS (m/z) 323.1 (M+H).
and
Methyl 2-[4-[5-amino-4-cyano-1-(1,1,1-trifluoropropan-2-yl)pyrazol-3-yl]phenyl]prop-2-enoate (2.00 g) is purified by Prep-HPLC with the following conditions: Column: N—(R,R)-Whelk-O1 4.6*50 mm, 3.5 μm; mobile phase A: mobile phase B: MeOH (0.1% DEA), with flow rate of 2 mL/min; eluting with 10% B, UV 254 nm; t(R) Isomer 1 is 6.7 min; t(R) Isomer 2 is 7.2; (700 mg, 35.0%, 100% ee) as a yellow solid and (700 mg, 35.0%, 100% ee) as a yellow solid.
The following compounds in Table 6 are prepared essentially as described for methyl 2-[4-[5-amino-4-cyano-1-[1,1,1-trifluoropropan-2-yl]pyrazol-3-yl]phenyl]prop-2-enoate, Isomer 1 and methyl 2-[4-[5-amino-4-cyano-1-[1,1,1-trifluoropropan-2-yl]pyrazol-3-yl]phenyl]prop-2-enoate, Isomer 2 using the appropriate purification conditions.
1CHIRALPAK IG, 2*25 cm, 5 μm; eluting with 30% EtOH in hexanes (10 mM NH3—MeOH), flow rate: 20 mL/min, UV 234/274 nm
2CHIRAL ART Amylose-SA, 2*25 cm, 5 μm; eluting with 10% EtOH in hexanes (0.5% 2 M NH3—MeOH) flow rate 20 mL/min, 210/220 nm.
3CHIRALPAK IH, 2.0*2.5 cm, 5 μm eluting with 40% EtOH in hexanes (10 mM NH3—MeOH), flow rate 20 mL/min, UV 235.275.
A mixture of methyl 2-[4-(5-amino-4-cyano-1-isopropyl-pyrazol-3-yl)phenyl]prop-2-enoate (43.00 g, 138.55 mmol) and 50% Pd/C (43.00 g) in MeOH (1 L) is stirred for 4 hrs at RT under N2. The resulting mixture is filtered (through diatomaceous earth if needed) and the filter cake is washed with MeOH (300 ml). The filtrate is concentrated under reduced pressure to give the title compound (40 g, 92.4%) as a yellow solid. ES/MS (m/z) 313.2 (M+H).
The following compounds in Table 7 are prepared essentially as described for methyl 2-[4-(5-amino-4-cyano-1-isopropylpyrazol-3-yl)phenyl]propanoate using the appropriate reagents, using a balloon of hydrogen if appropriate, using 10-50% Pd/C, and adjusting reaction times to determine completion of the reactions. The products can also be purified by silica gel chromatography eluting with a solvent system such as PE:EtOAc of 2:1 to 1:1.
1PD(OH)2/C is catalyst and DCM is solvent used
Methyl 2-[4-[5-amino-4-cyano-1-(1-methylcyclopropyl)pyrazol-3-yl]phenyl]prop-2-enoate (260 mg, 0.81 mmol), MeOH (15.00 mL) and 50% Pd/C (275 mg) are added together. The solution is stirred for 2 hrs at RT under H2. The mixture is filtered, and the solution is concentrated under vacuum to give the title compound (240 mg, 91%) as a light yellow solid. The crude product is used directly without further purification. ES/MS (m/z) 325.1 (M+H).
To a stirred solution of methyl 2-[4-(2,2-dicyano-1-methoxyeth-1-en-1-yl)phenyl]propanoate (4.00 g, 14.80 mmol) and (1-methylcyclopropyl)hydrazine hydrochloride (1.81 g, 14.80 mmol) in THF (50.00 mL) is added Et3N (7.49 g, 73.99 mmol) dropwise at RT under N2. The mixture is stirred for 1 hr at 50° C. under N2. The mixture is diluted with H2O (50 mL) and extracted with EtOAc (3×100 mL). The combined organic extracts are washed with brine (3×200 mL), dried over anhydrous Na2SO4, filtered, and the filtrate is concentrated under reduced pressure. The residue is purified by silica gel column chromatography, eluting with hexanes/EtOAc (5:1-1:1) to give the title compound (3.8 g, 79.16%) as an off-white solid. ES/MS (m/z) 325.2 (M+H).
To a solution of methyl 2-[4-[5-amino-4-cyano-1-(1-methylcyclopropyl)pyrazol-3-yl]-3-fluorophenyl]prop-2-enoate (410 mg, 1.21 mmol) in MeOH (10 mL) is added Pd/C (10%, 0.64 g). The mixture is hydrogenated at RT for 1 hr using a H2 balloon. The mixture is filtered, the filter cake is washed with MeOH (3×50 mL) and the filtrate is concentrated under reduced pressure to give the title compound (340 mg, 82.44%) as a dark yellow solid. ES/MS (m/z) 343.2 (M+H).
To a stirred mixture of methyl 2-[4-(2,2-dicyano-1-methoxyeth-1-en-1-yl)phenyl]propanoate (400.00 mg, 1.48 mmol) and (1,1,1-trifluoro-2-methylpropan-2-yl)hydrazine dihydrochloride (210.33 mg, 1.48 mmol) in EtOH (5.00 mL) is added Et3N (449.25 mg, 4.44 mmol) in portions at RT under N2. The resulting mixture is stirred for 2 hrs at 50° C. under N2. The mixture is allowed to cool to RT and concentrated under reduced pressure. The residue is purified by silica gel column chromatography, eluting with a gradient of PE/EtOAc (2/1 to 1/1) to give the title compound (270 mg, 47%) as an off-white solid. ES/MS (m/z) 381.2 (M+H).
The following compound in Table 8 is prepared essentially as described for methyl 2-[4-[5-amino-4-cyano-1-(1,1,1-trifluoro-2-methylpropan-2-yl)pyrazol-3-yl]phenyl]propanoate using the appropriate reagents, adjusting reaction times to determine completion of the reactions, and adjusting purification conditions if needed. The reaction can be stirred from RT-50° C. and used without purification.
Lithium; 2-[5-[5-(tert-butoxycarbonylamino)-4-cyano-1-isopropyl-pyrazol-3-yl]-2-pyridyl]propanoate
Methyl 2-[5-[5-(tert-butoxycarbonylamino)-4-cyano-1-isopropyl-pyrazol-3-yl]-2-pyridyl]propanoate (100 mg, 0.227 mmol), methyl 2-[5-[5-[bis(tert-butoxycarbonyl)amino]-4-cyano-1-isopropyl-pyrazol-3-yl]-2-pyridyl]propanoate (958 mg, 1.87 mmol) are added together in MeOH (8.20 mL). LiOH (142 mg, 5.69 mmol) is solubilized in H2O (2.46 mL) and is added to the mixture. The reaction mixture is stirred at RT for 18 hrs and concentrated under reduced pressure to give the title compound (926 mg, 111.39%).
A mixture of methyl 2-[4-(5-amino-4-cyano-1-isopropylpyrazol-3-yl)phenyl]propanoate (40.00 g, 128.05 mmol) and NaOH (25.61 g, 640.26 mmol) in MeOH (500 mL) and H2O (500 mL) is stirred for 5 hrs at 50° C. The mixture is allowed to cool to RT. The resulting mixture is concentrated under reduced pressure, diluted with H2O (500 mL), and the aqueous layer is extracted with EtOAc (2×300 mL). The aqueous layer is acidified to pH 3-4 with 6 N HCl and the resulting precipitated solids are collected by filtration, washed with H2O (3×50 mL), and dried under vacuum to give the title compound (34 g, 89.0%) as a light yellow solid. ES/MS (m/z) 299.2 (M+H).
The following compounds in Table 9 are prepared essentially as described for 2-[4-(5-amino-4-cyano-1-isopropylpyrazol-3-yl)phenyl]propanoic acid and stirring at RT until completion.
12 M NaOH used with no extra H2O, after acidification with potassium bisulfate, the mixture and is cooled at 0 °C. for 1 hr and the title compound is filtered, collected, dried, used directly without further purification.
To a stirred solution of methyl 2-(6-[5-amino-4-cyano-1-[1,1,1-trifluoropropan-2-yl]pyrazol-3-yl]pyridin-3-yl)propanoate, Isomer 2 (1.30 g, 3.53 mmol) in THF (16.00 mL) and H2O (4.00 mL) is added LiOH (253.56 mg, 10.59 mmol) in portions at RT under N2. The resulting mixture is stirred for 2 hrs at RT under N2. The mixture is concentrated under reduced pressure, diluted with H2O (20 mL), and acidified to pH 3 with HCl (c). The resulting mixture is extracted with EtOAc (3×50 mL). The combined organic extracts are washed with saturated aqueous NaCl solution (2×100 mL), dried over anhydrous Na2SO4, filtered, and concentrated under reduced pressure to give the title compound (1.2 g, 96%) as a light yellow solid. ES/MS (m/z) 353.9 (M+H).
The following compounds in Table 10 are prepared essentially as described for 2-(6-[5-amino-4-cyano-1-[−1,1,1-trifluoropropan-2-yl]pyrazol-3-yl]pyridin-3-yl)propanoic acid, Isomer 1 using the appropriate reagents at RT to 50° C. and adjusting reaction times to determine completion of the reactions. LiOH can be added portionwise or in a single amount depending on the scale of the reaction.
A solution of methyl 2-[4-[5-amino-4-cyano-1-[2,2,2-trideuterio-1-(trideuteriomethyl)ethyl]pyrazol-3-yl]phenyl]propanoate (630 mg, 1.98 mmol) and LiOH (143 mg, 5.94 mmol) in MeOH/H2O (25 mL, 4:1) is stirred for 1 hr at RT. The solution is extracted with EtOAc (2×5 mL). The aqueous layer is acidified with HCl (2 M) and extracted with EtOAc (3×50 mL). The organic extract is dried over anhydrous Na2SO4 and concentrated under reduced pressure to give the title compound (460 mg, crude) as a light yellow solid. The product is washed with Et2O (10 mL) used directly without further purification. ES/MS (m/z) 305.20 (M+H).
Methyl 2-[4-[5-amino-4-cyano-1-(1-methylcyclopropyl)pyrazol-3-yl]phenyl]propanoate (220.00 mg, 0.68 mmol), MeOH (2.00 mL), H2O (2.00 mL), and NaOH (109 mg, 2.71 mmol) are added together. The solution is stirred for 2 hrs at 50° C. and then MeOH is removed under reduced pressure. The pH of the mixture is adjusted to with 4 N HCl and the mixture is extracted with EtOAc (2×50 mL). The combined organic extracts are washed with H2O (2×15 mL), washed with brine (10 mL) and concentrated to give the title compound (240 mg, 100% crude) as an off-white solid. The crude product is used directly without further purification. ES/MS (m/z) 311.2 (M+H).
A solution of methyl 2-[4-[5-amino-4-cyano-1-(1-methylcyclopropyl)pyrazol-3-yl]-3-fluorophenyl]propanoate (340 mg, 0.99 mmol) and LiOH (118.91 mg, 4.96 mmol) in THF/H2O (4:1, 5.00 mL) is stirred for 1 hr at 50° C. under N2. The solution is cooled to RT and the mixture is acidified to pH=3 with HCl (aq. 1 N). The mixture is extracted with EtOAc (3×100 mL). The combined organic extracts are washed with brine (2×20 mL), dried over anhydrous Na2SO4, filtered, and the filtrate is concentrated under reduced pressure to give the title compound (280 mg, 85.87%) as a light yellow solid. ES/MS (m/z) 329.2 (M+H).
and
2-[4-(5-Amino-4-cyano-1-isopropylpyrazol-3-yl)phenyl]propanoic acid (500 mg) is separated by prep-chiral with the following conditions: Column: (R,R)Whelk-O1, 21.1*250 mm, 5 μm; mobile phase A: hexanes (0.1% FA), mobile phase B:IPA; eluting with a gradient of 0-30% B in 17 min at 20 mL/min; UV 254 nm; t(R) isomer 1 9.2 min (209.6 mg, 41.2%, 100% ee) as a white solid, ES/MS (m/z) 299.1 (M+H), t(R) isomer 2 12 min (206.8 mg, 41.03%, 100% ee) as a white solid, ES/MS (m/z) 299.1 (M+H).
and
2-[6-(5-Amino-4-cyano-1-isopropylpyrazol-3-yl)pyridin-3-yl]propanoic acid (290.00 mg) is separated by prep-chiral with the following conditions: Column: CHIRALPAK AD-H, 2.0*25 cm L; mobile phase A: hexanes (0.1% TFA), mobile phase B: IPA eluting with a gradient of 30%-0% B in 9.5 min; flow rate 20 mL/min; UV 230/254 nm, t(R) Isomer 1 6.2 min, (102.5 mg, 35.3%) as a white solid with 100% ee; ES/MS (m/z) 300.1 (M+H), t(R) Isomer 2 7.8 min (104.8 mg, 36.1%) as a white solid with 100% ee, ES/MS (m/z) 300.1 (M+H).
A mixture of 2-[4-(5-amino-4-cyano-1-isopropylpyrazol-3-yl)phenyl]propanoic acid (1.00 g, 3.352 mmol), NaOH (671 mg, 16.759 mmol) and H2O2 (7.81 mL, 68.873 mmol, 30%) in EtOH (20.00 mL)/DMSO (2.00 mL) is stirred overnight at 50° C. The reaction is quenched with saturated Na2SO3 aqueous (20 mL) at 0° C. The resulting mixture is diluted with H2O (200 mL) and acidified to pH 3-4 with 6 N HCl. The precipitated solids are collected by filtration and washed with H2O (2×10 mL). The solid is purified by reverse Combi-flash chromatography with the following conditions: column, C18; mobile phase, ACN in H2O eluting with a gradient of 30% to 60% in 25 min; detector, UV 220 nm and then lyophilized to give the title compound (670 mg, 62.5%) as an off-white solid. ES/MS (m/z) 317.2 (M+H).
and
2-[4-(5-Amino-4-carbamoyl-1-isopropylpyrazol-3-yl)phenyl]propanoic acid (280 mg) is separated by prep-chiral HPLC with the following conditions: Column: CHIRALPAK AD-H, 2.0*25 cm; mobile phase A: hexanes (0.1% FA), mobile phase B: IPA; flow rate: 20 mL/min eluting with 15% B in 21 min; UV 210Y254 nm; t(R) Isomer 1 16 min, (106.2 mg, 37.6%, 100% ee) as a white solid, ES/MS (m/z) 317.1 (M+H); t(R) Isomer 2 19 min, (94.96 mg, 33.3%, 98.3% ee) as a white solid, ES/MS (m/z) 317.1 (M+H).
A solution of 5,5-difluoro-4,4-dimethyl-3-oxohexanenitrile (1.50 g, 8.56 mmol), NaHCO3 (1.80 g, 21.427 mmol), and bis(hydroxylammonium); sulfate (1.69 g, 10.30 mmol) in H2O (27.00 mL) and MeOH (3.00 mL) is stirred overnight at 65° C. under N2. The mixture is used directly without further purification. ES/MS m/z 209.2 (M+H).
A solution of 3-(3,3-dimethylcyclobutyl)-3-oxopropanenitrile (1.50 g, 9.92 mmol), NH2OH.HCl (0.76 g, 10.94 mmol), and NaOH (0.79 g, 19.84 mmol) in H2O (15.00 mL) is stirred for 2 hrs at 100° C. under N2. The mixture is allowed to cool to RT. The precipitated solids are collected by filtration and washed with H2O (3×30 mL). The resulting mixture is concentrated under reduced pressure to give the title compound (1.5 g, 90.97%) as an off-white solid. ES/MS (m/z) 167.3 (M+H).
The following compound in Table 11 is prepared essentially as described for 3-(3,3-dimethylcyclobutyl)-1,2-oxazol-5-amine using the appropriate reagents and adjusting the reaction time to determine completion of the reaction. The base can be added in portions and the reaction mixture can be extracted with DCM or filtered as appropriate.
To a stirred mixture of 3-[3-methylbicyclo[1.1.1]pentan-1-yl]-3-oxopropanenitrile (350.00 mg, 2.41 mmol) and hydroxylamine HCl (183.83 mg, 2.65 mmol) in H2O (8.00 mL) is added NaOH (192.38 mg, 4.81 mmol) in portions at RT under N2. The mixture is stirred for 1 hr at 100° C. under N2. The mixture is allowed to cool to RT. The precipitated solids are collected by filtration and washed with H2O (3×20 mL), to give the title compound (300 mg, 77.9%) as a light yellow solid. ES/MS m/z (M+H) 165.1.
A solution of 3-(2,2-dimethylpropyl)-1,2-oxazol-5-amine (5.00 g, 32.42 mmol) and Selectfluor™ (13.78 g, 38.90 mmol) in MeOH (100 mL, 780.04 mmol) is stirred for 30 mins at 50° C. under N2. The reaction is cooled to RT, diluted with H2O (100 mL) and extracted with EtOAc (3×100 mL). The organic extract is dried over anhydrous Na2SO4 and concentrated under reduced pressure. The crude product is purified by silica gel chromatography (PE:EtOAc=10:1 to 5:1) to give the title compound (1.55 g, 27.7%) as a light yellow solid. LC-MS: (ES+H, m/z):[M+H]+=173.10
A mixture of 3-oxo-3-[3-(trifluoromethyl)bicyclo[1.1.1]pentan-1-yl]propanenitrile (280.00 mg, 1.38 mmol), hydroxylamine HCl (105.35 mg, 1.52 mmol) and H2O (10 mL) is added NaOH (110.25 mg, 2.76 mmol) in portions at RT under N2. The resulting mixture is heated to 100° C. for 1 hr. The mixture is allowed to cool to RT and is extracted with DCM (3×50 mL). The combined organic extracts are washed with brine, dried over anhydrous Na2SO4, filtered, and concentrated under reduced pressure. The resulting solid is triturated with Et2O (10 mL). The resulting solids are collected by filtration and washed with Et2O to give the title compound (220 mg, 73%). ES/MS m/z (M+H) 219.2.
The crude solution of (Z)-5,5-difluoro-N′-hydroxy-4,4-dimethyl-3-oxohexanimidamide is acidified to pH=1 with HCl (c) and the resulting mixture is stirred for 1 hr at 100° C. under N2. The mixture is slowly cooled to RT and concentrated under reduced pressure. The residue is purified by reversed combi-flash chromatography with the following conditions: Column, C18; mobile phase, ACN in H2O eluting with a 30% to 50% gradient in 20 min; UV 220 nm to give the title compound (230 mg, 14%) as a yellow solid. ES/MS (m/z) 191.2 (M+H).
To a crude mixture of 3-(2-chloro-4-fluorophenyl)-3,2-oxopropanenitrile (2.8 g, 14 mmol) is added NH2OH.HCl (0.98 g, 14.17 mmol), KOAc (2.09 g, 21.30 mmol) and 1,4-dioxane (30.00 mL). The resulting mixture is stirred at 100° C. overnight. The mixture is allowed to cool to RT and diluted with H2O (30 mL) and EtOAc (30 mL). The mixture is extracted with EtOAc (3×30 mL). The combined organic extracts are dried over anhydrous Na2SO4, filtered, and concentrated under reduced pressure. The residue is purified by silica gel column chromatography eluting with a gradient of PE/EtOAc (9:1-2:1) to give the title compound (1.2 g, 39.83%) as a yellow solid. ES/MS (m/z) (35Cl/37Cl) 213.0/215.0 (M+H).
The following compound in Table 12 is prepared essentially as described for 3-(2-chloro-4-fluorophenyl)-1,2-oxazol-5-amine using the appropriate reagents, adjusting the reaction time to determine completion of the reaction, and purification conditions as appropriate. The reaction temperature can range from about 70° C. to 100° C. NaOAc can be substituted for KOAc and EtOH can be substituted for 1,4-dioxane.
To a stirred mixture of 4,4-dimethyl-3-oxohexanenitrile (3.00 g, 21.55 mmol) and hydroxylamine sulfate (3.89 g, 23.71 mmol) in MeOH (5.00 mL) and H2O (45 mL) is added NaHCO3 (4.53 g, 53.88 mmol) in portions at RT under N2. The resulting mixture is stirred for 5 hrs at 65° C. under N2. The mixture is allowed to cool to RT. The mixture is acidified to pH 1 with HCl (c) and stirred for 20 min at 130° C. under N2. The mixture is allowed to cool to RT and the pH adjusted to 8 with NaOH. The resulting mixture is extracted with DCM (3×200 mL). The combined organic extracts are washed with saturated aqueous NaCl solution (2×200 mL), dried over anhydrous Na2SO4, filtered, and concentrated under reduced pressure. The residue is purified by reverse phase combi-flash chromatography with the following conditions: Column, C18; mobile phase, ACN in H2O (0.1% NH4HCO3), eluting with a 30% to 40% gradient in 10 min; UV 220 nm, to give the title compound (1.2 g, 36%) as a light yellow solid. 1H NMR (CDCl3) δ5.53 (s, 1H), 1.66 (q, 2H), 1.27 (s, 6H), 0.82 (t, 3H).
A solution of NH2OH.HCl (535.66 mg, 7.71 mmol) and KOAc (756.53 mg, 7.71 mmol) in MeOH (10.00 mL) is stirred for 1 hr at RT under N2. To the mixture is added 3-(2,4-dichlorophenyl)-3-oxopropanenitrile (550.00 mg, 2.57 mmol) and the reaction is stirred for an additional 1 hr at RT. The resulting mixture is filtered, the filter cake is washed with MeOH (3×20 mL), and the filtrate is concentrated under reduced pressure. The residue is diluted with H2O (30 mL) and the precipitated solids are collected by filtration, washed with H2O (3×20 mL), and dried under reduced pressure to give the title compound (200 mg, 35.0%) as a yellow solid. ES/MS m/z (35Cl/37Cl) 229.0/231.0 (M+H).
A solution of 3-(1,1,1-trifluoro-2-methylpropan-2-yl)-1H-pyrazol-5-amine (500.0 mg, 2.59 mmol), hexane-2,5-dione (886.3 mg, 7.77 mmol) and HOAc (15.5 mg, 0.26 mmol) in toluene (10.00 mL) is stirred for 2 hr at 100° C. under N2. The mixture is concentrated under reduced pressure. The residue is purified by reversed Combi-flash chromatography eluting with the following conditions: Column, C18 gel eluting with a gradient of 30% to 50% ACN in H2O (0.1% FA) over 10 min; UV 254 nm to give the title compound (610 mg, 87%) as a yellow solid. ES/MS m/z (M+H) 272.1.
A solution of 5-(2,5-dimethyl-1H-pyrrol-1-yl)-3-(1,1,1-trifluoro-2-methylpropan-2-yl)-1H-pyrazole (500.0 mg, 1.84 mmol), Mel (1046.4 mg, 7.37 mmol) and K2CO3 (509.4 mg, 3.69 mmol) in ACN (10.00 mL) is stirred for 4 hr at 80° C. under N2. The mixture is concentrated under reduced pressure. The residue is purified by Prep-TLC eluting with 5:1 PE/EtOAc, 254 nm to give the title compound (95 mg, 18%) as a white solid. ES/MS m/z (M+H) 286.2.
A solution of KOH (53.1 mg, 0.95 mmol) in EtOH (1.00 mL) and H2O (1.00 mL) is added to a solution of hydroxylamine HCl (131.5 mg, 1.89 mmol) in EtOH (2.00 mL). 3-(2,5-Dimethyl-1H-pyrrol-1-yl)-1-methyl-5-(1,1,1-trifluoro-2-methylpropan-2-yl)-1H-pyrazole (90.0 mg, 0.32 mmol) is added and the mixture is stirred for 4 hr at 100° C. under N2. The mixture is concentrated under reduced pressure. The residue is purified by reversed Combi-flash chromatography with the following conditions: Column, C18 gel eluting with a gradient of 10% to 30% ACN in H2O (0.1% FA) over 10 min; UV 254 nm to give the title compound (45 mg, 68%) as a white solid. ES/MS m/z (M+H) 208.1.
To a suspension of lithium; 2-[5-[5-(tert-butoxycarbonylamino)-4-cyano-1-isopropyl-pyrazol-3-yl]-2-pyridyl]propanoate (300 mg, 0.740 mmol) in pyridine (1.85 mL) under N2 is added MeTHF (1.85 mL), 5-(1,1-dimethylpropyl)isoxazol-3-amine (171 mg, 1.11 mmol) then T3P® solution in MeTHF (50%, 1413 mg, 2.22 mmol). The reaction mixture is stirred at RT overnight and then poured into a saturated aqueous solution of NH4Cl. The aqueous layer is extracted with EtOAc (2×). The combined organic extracts are washed with saturated aqueous NaCl solution, dried over Na2SO4, filtered, and concentrated under reduced pressure. The crude material is purified by silica gel flash chromatography eluting with a gradient of acetone in DCM from 1 to 10% to give the title compound (181.3 mg, 43%). 1H NMR (d6-DMSO) δ11.17 (s, 1H), 9.91 (s, 1H), 8.92 (d, J=2.3 Hz, 1H), 8.16 (dd, J=8.2, 2.4 Hz, 1H), 7.60 (d, J=8.2 Hz, 1H), 6.61 (s, 1H), 4.58 (p, J=6.5 Hz, 1H), 4.16 (q, J=6.9 Hz, 1H), 1.61 (q, J=7.5 Hz, 2H), 1.50 (d, J=8.4 Hz, 13H), 1.41 (d, J=6.6 Hz, 7H), 1.24 (s, 7H), 1.08 (s, 1H), 0.73 (t, J=7.5 Hz, 3H).
The following compounds in Table 13 are prepared essentially as described for tert-butyl N-[4-cyano-5-[6-[2-[[5-(1,1-dimethylpropyl)isoxazol-3-yl]amino]-1-methyl-2-oxo-ethyl]-3-pyridyl]-2-isopropyl-pyrazol-3-yl]carbamate adjusting the reaction time to determine completion of the reaction and using appropriate chromatography conditions for purification.
a
b
c
a1H NMR (400 MHz, d6-DMSO) δ 8.95-8.90 (m, 1H), 8.58 (dd, J = 5.8, 1.6 Hz, 1H), 8.17 (dd, J = 8.2, 2.4 Hz, 1H), 7.60 (d, J = 8.2 Hz, 1H), 7.39 (ddd, J = 7.6, 4.3, 1.5 Hz, 1H), 6.38 (s, 1H), 4.58 (p, J = 6.5 Hz, 1H), 4.17 (q, J =7.0 Hz, 1H), 1.55-1.46 (m, 20H), 1.41 (d, J = 6.6 Hz, 8H).
b1H NMR (400 MHz, d6-DMSO) δ 11.76 (s, 1H), 9.91 (s, 1H), 8.93 (d, J = 2.4 Hz, 1H), 8.17 (dd, J = 8.2, 2.4 Hz, 1H), 7.60 (d, J = 8.2 Hz, 1H), 6.12 (s, 1H), 4.58 (p, J = 6.6 Hz, 1H), 4.15 (q, J = 7.0 Hz, 1H), 2.45 (s, 2H), 1.52-1.49 (m, 12H), 1.41 (d, J = 6.6 Hz, 6H), 0.93 (s, 9H).
c2-[5-[5-(tert-Butoxycarbonylamino)-4-cyano-1-isopropyl-pyrazol-3-yl]-2-pyridyl]propanoic acid used instead of the lithium salt
To a mixture of 3-(2,2-dimethylpropyl)-1,2-oxazol-5-amine (62 mg, 0.402 mmol), 2-[4-(5-amino-4-cyano-1-isopropylpyrazol-3-yl)phenyl]propanoic acid (120 mg, 0.402 mmol), and NMI (99 mg, 1.206 mmol) in ACN (5.00 mL) is added TCFH (338 mg, 1.206 mmol). The resulting mixture is stirred at 50° C. for 2 hrs under N2 and then concentrated under reduced pressure. The residue is purified by reverse Combi-flash chromatography with the following conditions: Column, C18; mobile phase, ACN in H2O (0.1% NH4CO3) and eluting with a gradient of 0% to 50% in 25 min; UV 254 nm to give the title compound (130 mg, 74.41%) as a white solid. ES/MS (m/z) 435.2 (M+H).
The following compounds in Table 14 are prepared essentially as described for 2-[4-(5-amino-4-cyano-1-isopropylpyrazol-3-yl)phenyl]-N-[3-(2,2-dimethylpropyl)-1,2-oxazol-5-yl]propanamide using the appropriate reagents, adjusting reaction time to determine completion of the reaction, and purification conditions as appropriate. The reaction temperature can range from about 50° C. to 80° C.
To a stirred mixture of 2-[4-[5-amino-4-cyano-1-(1-methylcyclopropyl)pyrazol-3-yl]phenyl]propanoic acid (220 mg, 0.71 mmol) and 3-(2,2-dimethylpropyl)-1,2-oxazol-5-amine (131 mg, 0.85 mmol) in ACN (3.00 mL) is added NMI (291 mg, 3.54 mmol) and TCFH (995 mg, 3.54 mmol). The mixture is stirred for 3 hr at 50° C. The mixture is purified by reversed Combi-flash chromatography with following conditions: C18; eluting with a gradient of 50% to 80% ACN in H2O (0.1% FA) to give the title compound (200 mg, 63.1%) as an off-white solid. ES/MS (m/z) 447.3 (M+H).
To a stirred mixture of 2-[4-[5-amino-4-cyano-1-(1-methylcyclopropyl)pyrazol-3-yl]phenyl]propanoic acid (150 mg, 0.48 mmol) and 3-[3-methylbicyclo[1.1.1]pentan-1-yl]-1,2-oxazol-5-amine (79.36 mg, 0.48 mmol) in ACN (5.00 mL) is added NMI (119.05 mg, 1.45 mmol) and TCFH (271.22 mg, 0.97 mmol) in portions at RT under N2. The mixture is stirred for 2 hr at 50° C. under N2. The mixture is allowed to cool to RT and concentrated under reduced pressure. The residue is purified by silica gel column chromatography, eluting with PE/EtOAc (3/1 to 2/1) to give the title compound (130 mg, 58.9%) as an off-white solid. ES/MS (m/z) 457.2 (M+H).
To a solution of 2-[4-[5-amino-4-cyano-1-(1-methylcyclopropyl)pyrazol-3-yl]-3-fluorophenyl]propanoic acid (150 mg, 0.46 mmol), 3-[3-methylbicyclo[1.1.1]pentan-1-yl]-1,2-oxazol-5-amine (90.02 mg, 0.55 mmol) and NMI (112.52 mg, 1.37 mmol) in ACN (5.00 mL) is added TCFH (192.27 mg, 0.68 mmol). The reaction is stirred for 1 hr at 50° C. The mixture is allowed to cool to RT and concentrated under reduced pressure. The residue is purified by reversed Combi-flash chromatography with the following conditions: Column, C18; eluting with a gradient of 20% to 40% ACN in H2O (0.1% NH4HCO3) to give the title compound (110 mg, 50.74%) as a white solid. ES/MS (m/z) 475.1 (M+H).
To a solution of 2-[4-(5-amino-4-cyano-1-isopropylpyrazol-3-yl)phenyl]propanoic acid (300 mg, 1.01 mmol), 3-[3-(trifluoromethyl)bicyclo[1.1.1]pentan-1-yl]-1,2-oxazol-5-amine (264 mg, 1.21 mmol) and NMI (248 mg, 3.02 mmol) in ACN (20 mL), TCFH (1.41 g, 5.03 mmol) is added and the mixture is stirred for 1 hr at 50° C. under N2 in a sealed tube. The mixture is cooled to RT and concentrated under reduced pressure. The residue is purified by reserved phase Combi-flash chromatography with the following condition: Column, C18, eluting with a gradient of 10% to 50% ACN in H2O (0.1% NH4HCO3) to give the title compound (250 mg, 49.9%) as light brown solid. ES/MS (m/z) 499.10 (M+H).
To a stirred solution of 2-[4-[5-amino-4-cyano-1-[2,2,2-trideuterio-1-(trideuteriomethyl)ethyl]pyrazol-3-yl]phenyl]propanoic acid (700 mg, 2.30 mmol) and 3-(2,2-dimethylpropyl)-4-fluoro-1,2-oxazol-5-amine (435.62 mg, 2.53 mmol) in ACN (5.00 mL) is added NMI (1.89 g, 22.99 mmol) and TCFH (6.45 g, 22.99 mmol) dropwise at RT under N2. The mixture is stirred for 3 hrs at 50° C. under N2. The mixture is concentrated under reduced pressure. The residue is purified by silica gel column chromatography, eluting with PE:EtOAc (3:2-1:1) to give the title compound (400 mg, 39.93%) as an off-white solid. ES/MS (m/z) 459.2 (M+H).
T3P® (250 μL, 0.427 mmol, 50% solution in EtOAc) is added dropwise to a stirring solution of 2-[4-(5-amino-4-cyano-1-isopropylpyrazol-3-yl)phenyl]propanoic acid, Isomer 1 (51 mg, 0.171 mmol), 3-(3-bicyclo[1.1.1]pentanylmethyl)isoxazol-5-amine (28.1 mg, 0.171 mmol) and pyridine (27.7 μL, 0.342 mmol) in EtOAc (2 mL, 0.1 M). The reaction is stirred at RT for 18 hrs. The reaction mixture is partitioned between EtOAc (5 mL) and saturated aqueous NaCl solution (5 mL). The organic layer is isolated and concentrated to dryness. The crude product is purified by C18 HPLC eluting with H2O:ACN (5-95%) with 0.1% TFA to give the title compound as a salt. The free base of the desired product is formed by eluting the desired product through a cartridge of carbonate resin to give the title compound (10 mg, 0.0225 mmol, 13%). ES/MS (m/z) 445.2 (M+H).
To a solution of 2-(6-[5-amino-4-cyano-1-[1,1,1-trifluoropropan-2-yl]pyrazol-3-yl]pyridin-3-yl)propanoic acid, Isomer 2 (200 mg, 0.57 mmol), 3-(2-chloro-4-fluorophenyl)-1,2-oxazol-5-amine (180 mg, 0.84 mmol), and DIPEA (273 mg, 2.11 mmol) in DCM (15 mL) is added T3P® (2.24 g, 3.52 mmol, 50% in EtOAc) and the mixture is stirred overnight at 50° C. The reaction is cooled to RT and concentrated under reduced pressure. The residue is purified by reversed phase Combi-flash with the following conditions: Column, C18; mobile phase, ACN in H2O (0.1% NH4CO3) eluting with a gradient of 10% to 50% in 10 min; UV 254 nm to give the title compound (100 mg, 32.2%) as an off-white solid. ES/MS (m/z) 548.10 (M+H).
The following compounds in Table 15 are prepared essentially as described for 2-(6-[5-amino-4-cyano-1-[1,1,1-trifluoropropan-2-yl]pyrazol-3-yl]pyridin-3-yl)-N-[3-(2-chloro-4-fluorophenyl)-1,2-oxazol-5-yl]propanamide, Isomer 2 using the appropriate reagents, adjusting reaction time to determine completion of the reaction, and using appropriate chromatography conditions for purification. Temperature can range from RT to 80° C. and can be completed in a sealed tube if appropriate. Dimethylacetamide (DMA) can be substituted for DCM.
To a stirred mixture of 2-[4-[5-amino-4-cyano-1-(1-methylcyclopropyl)pyrazol-3-yl]phenyl]propanoic acid (400 mg, 1.29 mmol) and 3-[3-(trifluoromethyl)bicyclo[1.1.1]pentan-1-yl]-1,2-oxazol-5-amine (281.20 mg, 1.29 mmol) in DCM (5.00 mL) is added DIPEA (499.72 mg, 3.87 mmol) and T3P® (4.10 g, 6.44 mmol, 50 wt % in EtOAc) dropwise in sealed tube at RT under N2. The mixture is stirred for 1 hr at 80° C. under N2. The mixture is concentrated under reduced pressure. The residue is purified by reverse combi-flash chromatography with the following conditions: C18; eluting with a gradient of 30% to 50% ACN in H2O to give the title compound (230 mg, 34%) as a light yellow solid. ES/MS (m/z) 511.2 (M+H).
2-[4-(5-Amino-4-cyano-1-isopropylpyrazol-3-yl)phenyl]propanoic acid, Isomer 1 (78 mg, 0.25 mmol), 3-(3-methylbicyclo[1.1.1]pentan-1-yl)isoxazol-5-amine (34 mg, 0.21 mmol) and 1-methylimidazole (39 mg, 0.038 mL, 0.48 mmol) are combined in EtOAc (3 mL). The orange solution is stirred for 2 mins at RT then T3P® (0.31 g, 0.29 mL, 50% Wt in EtOAc, 0.49 mmol) is added. The reaction is stirred for 16 hrs. The reaction is then diluted with 5 mL H2O and extracted with EtOAc (3×25 mL). The combined organic extracts are dried over Na2SO4, and the solvent is removed under reduced pressure. The residue is used without further purification. ES/MS (m/z) 511.2 (M+H). ES/MS (m/z) 445.2 (M+H).
tert-Butyl N-[4-cyano-2-isopropyl-5-[6-[1-methyl-2-oxo-2-[[5-(2,2,2-trifluoro-1,1-dimethyl-ethyl)isoxazol-3-yl]amino]ethyl]-3-pyridyl]pyrazol-3-yl]carbamate (130 mg, 0.226 mmol) and platinate(2-), tris(dimethylphosphinito-P)hydro-, dihydrogen (Parkins catalyst, CAS #173416-05-2) (116 mg, 0.271 mmol) are added together in a mixture of tert-BuOH (2.6 mL) and H2O (1.3 mL). The reaction mixture is stirred at 60° C. overnight, filtered through a pad of talcum powder, and washed with EtOAc. The organic phase is washed with H2O and the aqueous phase is extracted with EtOAc. The organic extracts are combined, dried over Na2SO4, filtered, and concentrated under vacuum to give the title compound as a white solid (147.8 mg, 104.73%). The material is used directly without purification.
The following compounds in Table 16 are prepared essentially as described for tert-butyl N-[4-carbamoyl-2-isopropyl-5-[6-[1-methyl-2-oxo-2-[[5-(2,2,2-trifluoro-1,1-dimethyl-ethyl)isoxazol-3-yl]amino]ethyl]-3-pyridyl]pyrazol-3-yl]carbamate using the appropriate reagents, adjusting reaction time to determine completion of the reaction and using appropriate chromatography conditions for purification if needed. Temperature can vary from about 60 to 70° C.
1EtOH can be substituted for tert-BuOH.
To a mixture of 2-[4-(5-amino-4-cyano-1-isopropylpyrazol-3-yl)phenyl]-N-[3-(2,2-dimethylpropyl)-1,2-oxazol-5-yl]propanamide (120 mg, 0.276 mmol), NaOH (55 mg, 1.38 mmol), H2O (2.00 mL), and DMSO (1.00 mL) in EtOH (5.00 mL) is added H2O2 (187.86 mg, 5.523 mmol, 30% aq.). The resulting mixture is stirred at 40° C. for 4 hrs. The mixture is allowed to cool to RT and quenched by the addition of saturated Na2SO3 aqueous (10 mL). The mixture is extracted with EtOAc (3×50 mL). The combined organic extracts are washed with saturated aqueous NaCl solution (50 mL), dried over anhydrous Na2SO4, filtered, and concentrated under reduced pressure. The residue is purified by reverse Combi-flash chromatography with the following conditions: Column, C18; mobile phase ACN in H2O (0.1% NH4CO3) eluting with a gradient of 0% to 50% in 25 min; UV 254 nm to give the title compound (100 mg, 80.02%) as a white solid. ES/MS (m/z) 453.4 (M+H).
The following compounds in Table 17 are prepared essentially as described for 5-amino-3-[4-(1-[[3-(2,2-dimethylpropyl)-1,2-oxazol-5-yl]carbamoyl]ethyl)phenyl]-1-isopropylpyrazole-4-carboxamide using the appropriate reagents, adjusting reaction time to determine completion of the reaction and using appropriate chromatography conditions for purification. NaOH and H2O2 can be added in portions and the relative amounts of solvents H2O, EtOH, and DMSO may be varied. Temperature can vary from RT to 50° C.
A mixture of 2-[4-(5-amino-4-carbamoyl-1-isopropylpyrazol-3-yl)phenyl]propanoic acid (1.30 g, 4.109 mmol), 3-(2,2-dimethylpropyl)-1,2-oxazol-5-amine (0.70 g, 4.520 mmol), NMI (2.12 g, 16.437 mmol) and TCFH (2.31 g, 8.218 mmol) in DMF (50 mL) is stirred for 4 hrs at RT under N2. The mixture is diluted with H2O (200 mL) and extracted with EtOAc (3×200 mL). The combined organic extracts are washed with saturated aqueous NaCl solution (3×100 mL) and concentrated under reduced pressure. The residue is purified by reverse Combi-flash chromatography with the following conditions: column, C18; mobile phase, ACN in H2O (0.1% FA) eluting with a gradient of 55% to 65% in 10 min; UV 220 nm to give the title compound (500 mg, 26.9%) as a light yellow solid. ES/MS (m/z) 453.4 (M+H).
To a mixture of 2-[6-(5-amino-4-cyano-1-isopropylpyrazol-3-yl)pyridin-3-yl]-N-[3-(2,2-dimethylpropyl)-1,2-oxazol-5-yl]propanamide (120 mg, 0.28 mmol), NaOH (55 mg, 1.38 mmol), DMSO (0.40 mL), H2O (0.80 mL) in EtOH (2.00 mL) is added H2O2 (937 mg, 8.27 mmol 30%). The mixture is stirred at 40° C. for 4 hrs. The mixture is allowed to cool to RT, quenched by the addition of saturated Na2SO3 (aq 30 mL) and extracted with EtOAc (3×50 mL). The combined organic extracts are washed with brine (50 mL), dried over anhydrous Na2SO4, filtered, and concentrated under reduced pressure. The residue is purified by reversed Combi-flash chromatography with the following conditions: Column, C18, eluting with a gradient of 0 to 50% ACN in H2O (0.1% NH4CO3) to give the title compound (100 mg, 80%) as a white solid. ES/MS (m/z) 454.2 (M+H).
2-[4-[5-Amino-4-cyano-1-(1-methylcyclopropyl)pyrazol-3-yl]phenyl]-N-[3-(2,2-dimethylpropyl)-1,2-oxazol-5-yl]propanamide (190 mg, 0.43 mmol), EtOH (5.00 mL), H2O (2.00 mL), DMSO (1.00 mL), NaOH (170.00 mg, 4.26 mmol) and H2O2 (2.43 g, 21.30 mmol, 30%) are added together. The solution is stirred for 5 hrs at 40° C. The reaction is quenched by saturated Na2SO3 (10 mL). The solution is diluted with EtOAc (100 mL), washed with H2O (2×30 mL), and brine (20 mL). The organic phase is concentrated under reduced pressure. The residue is purified by reversed Combi-flash chromatography with following conditions: C18; eluting with a gradient of 50% to 80% ACN in H2O (0.1% NH4CO3) to give the title compound (190 mg, 95.9%) as a white solid. ES/MS (m/z) 465.3 (M+H).
To a stirred solution of 2-[4-[5-amino-4-cyano-1-(1-methylcyclopropyl)pyrazol-3-yl]phenyl]-N-[3-[3-(trifluoromethyl)bicyclo[1.1.1]pentan-1-yl]-1,2-oxazol-5-yl]propanamide (225.00 mg, 0.44 mmol) in EtOH (5.00 mL) and DMSO (1.00 mL) is added NaOH (176.28 mg, 4.41 mmol) and H2O2 (30%, 999.40 mg, 8.82 mmol, 30 wt %) in portions at RT under N2. The mixture is stirred for 2 hr at 50° C. in sealed tube under N2. The mixture is cooled down to RT. The reaction is quenched by the addition of saturated Na2SO3 (20 mL) at RT. The mixture is extracted with EtOAc (3×50 mL). The combined organic extracts are washed with brine (2×100 mL), dried over anhydrous Na2SO4, and concentrated under reduced pressure. The residue is purified by reverse combi-flash chromatography with the following conditions: column, C18; eluting with a gradient of 40% to 50% ACN in H2O (0.1% NH4HCO3) to give the title compound (70 mg, 30%) as a white solid. ES/MS (m/z) 529.2 (M+H)
To a stirred solution of 2-[4-[5-amino-4-cyano-1-(1-methylcyclopropyl)pyrazol-3-yl]phenyl]-N-(3-[3-methylbicyclo[1.1.1]pentan-1-yl]-1,2-oxazol-5-yl)propanamide (130 mg, 0.29 mmol) in EtOH (5.00 mL) and DMSO (1.00 mL) is added NaOH (113.89 mg, 2.85 mmol) and H2O2 (30%, 645.70 mg, 5.70 mmol, 30 wt %) in portions at RT under N2. The mixture is stirred for 4 hr at 50° C. under N2. The mixture is allowed to cool to RT and quenched by the addition of saturated Na2SO3 (30 mL) at RT. The mixture is extracted with DCM (3×50 mL) and the combined organic extracts are washed with brine (2×100 mL), dried over anhydrous Na2SO4, filtered, and the filtrate is concentrated under reduced pressure. The residue is purified by reverse combi-flash chromatography with the following conditions: Column, C18; eluting with a gradient of 40% to 50% ACN in H2O (0.1% NH4HCO3) to give the title compound (95 mg, 70%) as a pink solid. ES/MS (m/z) 497.2 (M+Na).
A solution of 2-[4-(5-amino-4-cyano-1-isopropylpyrazol-3-yl)phenyl]-N-[1-methyl-5-(1,1,1-trifluoro-2-methylpropan-2-yl)pyrazol-3-yl]propanamide (130 mg, 0.27 mmol), NaOH (53.33 mg, 1.33 mmol) in EtOH/DMSO (6 mL, 5:1), H2O2 (907 mg, 7.99 mmol, 30%) is added together and stirred for 2 hrs at 50° C. The solution is cooled to RT, quenched with saturated Na2SO3 solution (10 mL) and extracted with EtOAc (3×20 mL), the organic extracts are dried over anhydrous Na2SO4 and concentrated under reduced pressure. The crude product is purified by reversed phase Combi-flash with the following condition: Column, C18; eluting with a gradient of 40% to 60% ACN in H2O (0.1% NH4HCO3), to give the title compound (100 mg, 74.18%). ES/MS (m/z) 506.4 (M+H).
To a solution of 2-[4-[5-amino-4-cyano-1-(1-methylcyclopropyl)pyrazol-3-yl]-3-fluorophenyl]-N-(3-[3-methylbicyclo[1.1.1]pentan-1-yl]-1,2-oxazol-5-yl)propanamide (100 mg, 0.21 mmol) and NaOH (42.14 mg, 1.05 mmol) in EtOH (5.00 mL) and DMSO (1.00 mL) is added H2O2 (358.39 mg, 3.161 mmol, 30%). The reaction is stirred for 2 hrs at 50° C. The reaction is quenched with saturated Na2SO3 (aq. 10 mL) at 0° C. The aqueous layer is extracted with EtOAc (3×30 mL). The combined organic layers are washed with brine (2×20 mL), dried over anhydrous Na2SO4, filtered, and the filtrate is concentrated under reduced pressure. The residue is purified by reversed Combi-flash chromatography with the following conditions: Column, C18; eluting with a gradient of 20% to 40% ACN in H2O (0.1% NH4HCO3) to give the title compound (70 mg, 67.44%) as a white solid. ES/MS (m/z) 493.2 (M+H).
A solution of 2-[4-(5-amino-4-cyano-1-isopropylpyrazol-3-yl)phenyl]-N-[3-[3-(trifluoromethyl)bicyclo[1.1.1]pentan-1-yl]-1,2-oxazol-5-yl]propanamid (230 mg, 0.46 mmol), H2O2 (1.05 g, 9.23 mmol, 30%) and NaOH (93 mg, 2.31 mmol) in EtOH/DMSO (20 mL, 4:1) is stirred for 2 hr at 40° C. The solution is cooled to RT, saturated Na2SO3 solution (10 mL) is added and the mixture is stirred for 10 mins at RT. The mixture is concentrated under reduced pressure and purified by reversed phase Combi-flash with the following condition: Column, C18; eluting with a gradient of 20% to 50% MeOH in H2O (0.1% NH4HCO3) to give the title compound (166 mg, 69.7%) as white solid. ES/MS (m/z) 517.10 (M+H).
To a stirred solution of 2-[4-[5-amino-4-cyano-1-[2,2,2-trideuterio-1-(trideuteriomethyl)ethyl]pyrazol-3-yl]phenyl]-N-[3-(2,2-dimethylpropyl)-4-fluoro-isoxazol-5-yl]propanamide (400 mg, 0.87 mmol) in EtOH (5.00 mL) and DMSO (1.00 mL) is added NaOH (174.44 mg, 4.36 mmol) and H2O2 (1.98 g, 17.45 mmol 30 wt %) dropwise at RT under N2. The mixture is stirred for 1 hr at 50° C. under N2 and then is quenched with saturated Na2SO3. The mixture is extracted with EtOAc (3×100 mL). The combined organic extracts are washed with brine (3×100 mL), dried over anhydrous Na2SO4, filtered, and concentrated under reduced pressure. The residue is purified by reverse combi-flash chromatography with the following conditions: Column C18; eluting with 30% to 50% ACN in H2O to give the title compound (120.00 mg, 28.87%) as a yellow solid. ES/MS (m/z) 477.3 (M+H).
To tert-butyl N-[4-carbamoyl-5-[6-[2-[[3-(1,1-dimethylpropyl)isoxazol-5-yl]amino]-1-methyl-2-oxo-ethyl]-3-pyridyl]-2-isopropyl-pyrazol-3-yl]carbamate (134 mg, 0.242 mmol) in DCM (1.45 mL) is added TFA (0.72 mL, 9.68 mmol). The reaction mixture is stirred at RT for 3 hrs. The reaction mixture is quenched with cold saturated aqueous solution of NaHCO3 and the aqueous layer is extracted with EtOAc. The combined organic extract is washed with saturated aqueous NaCl solution, dried over Na2SO4, filtered, and concentrated under reduced pressure. The crude material is purified by silica gel flash chromatography eluting with a gradient of MeOH in DCM from 0% to 5% to give the title compound (68 mg, 61.95%).
The following compounds in Table 18 are prepared essentially as described for 5-amino-3-[6-[2-[[3-(1,1-dimethylpropyl)isoxazol-5-yl]amino]-1-methyl-2-oxo-ethyl]-3-pyridyl]-1-isopropyl-pyrazole-4-carboxamide adjusting reaction time to determine completion of the reaction and using appropriate chromatography conditions for purification. The product can also be triturated in isopropyl ether, filtered, and dried under vacuum.
and
5-Amino-3-[4-(1-[[3-(2,2-dimethylpropyl)-1,2-oxazol-5-yl]carbamoyl]ethyl)phenyl]-1-isopropylpyrazole-4-carboxamide (100.00 mg, 0.22 mmol) is separated by prep-chiral chromatography with the following conditions: Column: CHIRAL ART Cellulose-SB, 2*25 cm, 5 μm; mobile phase A: hexanes (10 mM NH3), mobile phase B:IPA; flow rate 20 mL/min; eluting 30% B in 15 min; 254 nm; t(R) Isomer 1 is 8.2 min (33.3 mg, 33.3%), [α]D20=0.22696° (C=0.1, MeOH) as a white solid with 100% ee. t(R) Isomer 2 is 11.0 min (33.1 mg, 33.1%), [α]D20=−0.2113° (C=0.1, MeOH) as a white solid with 100% ee. ES/MS (m/z) 453.4 (M+H).
The following compounds in Table 19 are prepared essentially as described for 5-amino-3-[4-(1-[[3-(2,2-dimethylpropyl)-1,2-oxazol-5-yl]carbamoyl]ethyl)phenyl]-1-isopropylpyrazole-4-carboxamide, Isomer 1 and Isomer 2 and adjusting the purification system as appropriate.
1Column Chiralpak AD-H, 2*25 cm, 5 μm.
2Column: (R,R)Whelk-O 1, 21.1*250 mm, 5 μm.
3Column: (R,R)Whelk-O 1, Kromasil(02), 5*25 cm, 5 μm.
4CHIRALPAK IF, 2*25 cm, 5 μm.
5CHIRALPAK IA, 2*25 cm, 5 μm.
6CHIRALPAK IA, 2*25 cm, 5 μm.
7Mobile phase B, EtOH.
8(R,R)-Whelk-01, 2.12*25, 5 μm, mobile phase B, EtOH.
9Eluting with 25% IPA, 246/210 nm
5-Amino-3-[4-(1-[[3-(2,2-dimethylpropyl)-1,2-oxazol-5-yl]carbamoyl]ethyl)phenyl]-1-isopropylpyrazole-4-carboxamide (17 g) is isolated by prep-chiral with the following conditions: Column: CHIRAL ART Cellulose-SB, 2*25 cm, 5 μm; mobile phase A hexanes (10 mM NH3-MeOH), mobile phase B IPA; flow rate 20 mL/min; eluting with 30% B in 12 min; UV 254/220 nm; t(R) Isomer 1 is 7.0. The resulting solution is concentrated under reduced pressure. The residue is purified by reverse Combi-flash chromatography with the following conditions: column, C18; mobile phase, ACN in H2O (0.1% FA) eluting with a gradient of 55% to 65% in 10 min; UV 220 nm, (6.1315 g, 35.7%) as white solid with 99.8% ee, MP 128° C., ES/MS (m/z) 453.2 (M+H).
and
5-Amino-3-(4-[1-[(3-[3-methylbicyclo[1.1.1]pentan-1-yl]-1,2-oxazol-5-yl)carbamoyl]ethyl]phenyl)-1-(1-methylcyclopropyl)pyrazole-4-carboxamide (93 mg) is purified by Prep-HPLC with the following conditions: Column CHIRAL ART Cellulose-SB, 2*25 cm, 5 μm; eluting with 20% IPA in hexanes (10 mM NH3-MeOH), flow rate 20 mL/min; 254/210 nm to give Isomer 1, t(R) 12.22, (30.8 mg, 33% yield, 100% ee) as a white solid, ES/MS (m/z) 475.3 (M+H) and Isomer 2, t(R) 16.56, (30.5 mg, 33% yield 100% ee) as a white solid, ES/MS (m/z) 475.3 (M+H).
and
5-Amino-1-isopropyl-3-[4-(1-[[1-methyl-5-(1,1,1-trifluoro-2-methylpropan-2-yl)pyrazol-3-yl]carbamoyl]ethyl)phenyl]pyrazole-4-carboxamide (90 mg) is purified by Prep-CHIRAL-HPLC with the following conditions: Column CHIRALPAK IC, 2*25 cm, 5 μm; eluting with 30% IPA in hexanes (10 mM NH3-MeOH), flow rate 20 mL/min; 240/210 nm to give the title compound of Isomer 1, t(R) 15.48, (35.2 mg, 39.22% yield, 100% ee), ES/MS (m/z) 506.3 (M+H) as a white solid and the title compound of Isomer 2, t(R) 20.74, (32.3 mg, 35.89% yield 97.7% ee), ES/MS (m/z) 506.3 (M+H) as a white solid.
2-[4-(5-Amino-4-cyano-1-isopropyl-pyrazol-3-yl)phenyl]-N-[3-(3-methyl-1-bicyclo[1.1.1]pentanyl)isoxazol-5-yl]propanamide, Isomer 1 (110 mg, 247 μmol) and Parkins catalyst (106 mg, 247 μmol) are combined in EtOH (4 mL) and H2O (1 mL). The mixture is heated to 60° C. for 24 hrs. The mixture is passed through a 0.45 μM filter and the solvent is removed under reduced pressure. The residue is purified via silica gel flash chromatography eluting with a gradient of 0-100% heptane:EtOAc to give the title compound (26 mg, 23%) as a yellow solid. ES/MS (m/z) 463.2 (M+H).
and
5-Amino-1-(1-methylcyclopropyl)-3-[4-[1-([3-[3-(trifluoromethyl)bicyclo[1.1.1]pentan-1-yl]-1,2-oxazol-5-yl]carbamoyl)ethyl]phenyl]pyrazole-4-carboxamide (68 mg) is purified by Prep-CHIRAL-HPLC with the following conditions: Column: CHIRAL ART Cellulose-SB, 2*25 cm, 5 μm; eluting with 15% EtOH in hexanes (10 mM NH3-MeOH), flow rate 20 mL/min in 18 min, 254/210 nm to give the title compound of Isomer 1, t(R) 11.72, (15.3 mg, 22% yield with 100% ee) as a white solid, ES/MS (m/z) 529.2 (M+H) and the title compound of Isomer 2, t(R) 14.41, (16.8 mg, 24% yield with 100% ee) as a white solid, ES/MS (m/z) 529.2 (M+H).
The following compounds in Table 19a are prepared essentially as described for 5-amino-1-(1-methylcyclopropyl)-3-[4-[1-([3-[3-(trifluoromethyl)bicyclo[1.1.1]pentan-1-yl]-1,2-oxazol-5-yl]carbamoyl)ethyl]phenyl]pyrazole-4-carboxamide, Isomer 1 and Isomer 2 and adjusting chromatography conditions as appropriate.
1Eluting with 10% EtOH in 1:1 hexanes:MTBE (0.5% 2M NH3—MeOH).
2Eluting with 10% EtOH in hexanes (10 mM NH3—MeOH), 245/210 nm.
3Column: CHIRALPAK ID 2*25 cm, 5 μm; eluting with 8% IPA in 1:1 hexanes:MTBE (0.5% 2M NH3—MeOH), 245/210 nm.
4UV 245/210 nm.
and
5-Amino-3-(2-fluoro-4-[1-[(3-[3-methylbicyclo[1.1.1]pentan-1-yl]-1,2-oxazol-5-yl)carbamoyl]ethyl]phenyl)-1-(1-methylcyclopropyl)pyrazole-4-carboxamide (70 mg) is purified by Prep-Chiral-HPLC by following conditions: Column CHIRAL ART Cellulose-SB, 2*25 cm, 5 μm eluting with 30% IPA in hexanes (10 mM NH3-MeOH), 250/210 nm to give the title compound of Isomer 1 t(R) 7.04, (20.3 mg, 29.0%, 99.76% ee) as a white solid, ES/MS (m/z) 454.2 (M+H) and the title compound of Isomer 2 trio 9.48, (18.9 mg, 27.0%, 99.26% ee) as a white solid, ES/MS (m/z) 454.2 (M+H).
and
5-Amino-1-isopropyl-3-[4-[1-([3-[3-(trifluoromethyl)bicyclo[1.1.1]pentan-1-yl]-1,2-oxazol-5-yl]carbamoyl)ethyl]phenyl]pyrazole-4-carboxamide (162 mg) is purified by Prep-Chiral-HPLC by following conditions: Column CHIRAL ART Cellulose-SB, 2*25 cm, 5 μm eluting with 20% EtOH in hexanes (10 mM NH3-MeOH), 254/210 nm to give the title compound of Isomer 1 t(R) 10.66, (48.1 mg, 29.6%, 100% ee) as a white solid, ES/MS (m/z) 517.05 (M+H) and the title compound of Isomer 2 t(R) 13.23, (50.4 mg, 30.6%, 99.74% ee) as a white solid, ES/MS (m/z) 517.05 (M+H).
The following compounds in Table 19b are prepared essentially as described for 5-amino-1-isopropyl-3-[4-[1-([3-[3-(trifluoromethyl)bicyclo[1.1.1]pentan-1-yl]-1,2-oxazol-5-yl]carbamoyl)ethyl]phenyl]pyrazole-4-carboxamide, Isomer 1 and Isomer 2 and adjusting chromatography conditions as appropriate.
1UV is 210/237 nm
and
5-Amino-3-[4-[2-[[3-(2,2-dimethylpropyl)-4-fluoro-isoxazol-5-yl]amino]-1-methyl-2-oxo-ethyl]phenyl]-1-[2,2,2-trideuterio-1-(trideuteriomethyl)ethyl]pyrazole-4-carboxamide (120 mg) is purified by Prep-Chiral-HPLC by following conditions: Column CHIRAL ART Cellulose-SB, 2*25 cm, 5 μm eluting with 20% EtOH in hexanes (10 mM NH3-MeOH), 213/237 nm to give the title compound of Isomer 1 t(R) 7.78, (22.2 mg, 18.5%, 100% ee) as a beige solid, ES/MS (m/z) 477.25 (M+H) and the title compound of Isomer 2 t(R) 9.43, (27.1 mg, 22.6%, 98.14% ee) as a beige solid, ES/MS (m/z) 477.25 (M+H).
and
5-Amino-3-[5-(1-[[3-(2,2-dimethylpropyl)-1,2-oxazol-5-yl]carbamoyl]ethyl)pyridin-2-yl]-1-isopropylpyrazole-4-carboxamide (97.00 mg, 0.21 mmol) is separated by prep-chiral chromatography with the following conditions: Column: CHIRAL ART Cellulose-SB, 2*25 cm, 5 μm; mobile phase A: hexanes (10 mM NH3), mobile phase B: EtOH; flow rate 20 mL/min; eluting with 40% B in 11 min; 254/220 nm; t(R) Isomer 1 is 5.2 min (35.8 mg, 36.9%) as a white solid with 100% ee. ES/MS (m/z) 454.2 (M+H). t(R) Isomer 2 is 7.5 min (42.1 mg, 43.4%) as a white solid with 100% ee. ES/MS (m/z) 454.2 (M+H).
The following compounds in Table 20 are prepared essentially as described for 5-amino-3-[5-(1-[[3-(2,2-dim ethylpropyl)-1,2-oxazol-5-yl]carbamoyl]ethyl)pyridin-2-yl]-1-isopropylpyrazole-4-carboxamide, Isomer 1 and Isomer 2 and adjusting the purification system as appropriate.
1Column CHIRAL ART Cellulose-SB, S-5 μm, 50*250 mm, 5 μm.
2Column CHIRAL ART Cellulose-SB S-5 μm, 2*25 cm.
3Column CHIRALCEL OD-H, 2*25 mm.
4Column CHIRALCEL OD-H, 4.6X150 mm, 5 μm, 25% EtOH/CO2, 5 mL/min, 225 nm.
5Column CHIRAL ART Cellulose-SC.
6Column: (R,R)Whelk-O 1, 21.1*250 mm, 5 μm.
7Column: (R,R)Whelk-O1, 2.12*25 cm, 5 μm.
8EtOH used for mobile phase A and B, 50% isocratic.
9Column: CHIRALPAK IH, 25*2 cm, 5 μm, mobile phase A CO2, mobile phase B IPA, isocratic 45% B.
10(R,R)-Whelk-01, 2*25 mm, 5 μm.
11Column: Chiralpak AD-H, 2*25 cm, 5 μm.
12Column: Chiralpak AD-H, 2*25 cm, 5 μm, eluting with a gradient of 50% B to 0 B.
13Column: Chiralpak ADH, 2*25 cm, 5 μm, eluting with hexanes (10 mM NH3MeOH and 30% IPA.
14Solvent system is 30% EtOH in hexanes (10 mM NH3—MeOH).
15Column: CHIRALPAK IG, 2*25 cm, 5 μm; eluting with 30% EtOH in hexanes (10 mM NH3—MeOH), flow rate 20 mL/min, 234/274 nm.
16Column: CHIRAL ART Amylose-C NEO, 2.0*2 cm, 5 μm; eluting with 40% EtOH in hexanes (10 mM NH3—MeOH), flow rate 20 mL/min, 245/254 nm.
and
5-Amino-3-[4-[1-[[3-(2,2-dimethylpropyl)-1,2-oxazol-5-yl]carbamoyl]ethyl]phenyl]-1-(1-methylcyclopropyl)pyrazole-4-carboxamide (95 mg) is separated with the following conditions: Column: (R,R)-Whelk-O1, 2.12*25 cm, 5 μm; eluting with 30% EtOH in hexanes (10 mM-MeOH), flow rate 20 mL/min, UV 254 nm to give the title compound of Isomer 1 t(R) 11.5 min, (38.6 mg, 40.6%, 100% ee) as a white solid, ES/MS (m/z) 465.3 (M+H) and the title compound of Isomer 2 trio 20 min (30.7 mg, 32.3%, 99.6% ee) as a white solid, ES/MS (m/z) 465.3 (M+H).
and
5-Amino-3-(4-[1-[(5-tert-butyl-1,2-thiazol-3-yl)carbamoyl]ethyl]phenyl)-1-isopropylpyrazole-4-carboxamide (90 mg, 0.20 mmol) is separated by prep-chiral chromatography with the following conditions: Column: CHIRALPAK IG-3, 4.6*50 mm, 3.0 μm, mobile phase A: hexanes (0.1% DEA); mobile phase B: EtOH eluting with a gradient of 70% to 30% B; flow rate 1 mL/min, UV 254 nm, t(R) Isomer 1 is 2.1 min (25 mg, 21.8%) as a white solid, t(R) Isomer 2 is 3.3 min (25 mg, 21.8%) as a white solid. ES/MS (m/z) 455.25 (M+H).
and
5-Amino-1-isopropyl-3-[4-(1-[[5-(1,1,1-trifluoro-2-methylpropan-2-yl)-1,2-oxazol-3-yl]carbamoyl]ethyl)phenyl]pyrazole-4-carboxamide (90 mg, 0.18 mmol) is separated by prep-chiral chromatography with the following conditions: Column: CHIRALPAK IE, 2*25 cm, 5 μm; mobile phase A: ACN; mobile phase B: MtBE eluting with 25% B; 210 nm, 254 nm; t(R) Isomer 1 is 5 min (39.3 mg, 43.6%, 100% ee) as a white solid. t(R) Isomer 2 is 6 min (36.1 mg, 40.1%, 100% ee) as a white solid. ES/MS (m/z) 493.3 (M+H).
and
5-Amino-3-[6-[2-[[3-(1,1-dimethylpropyl)isoxazol-5-yl]amino]-1-methyl-2-oxo-ethyl]-3-pyridyl]-1-isopropyl-pyrazole-4-carboxamide (68 mg, 0.18 mmol) is chirally separated with the following conditions: Column: Acquity UPLC CSH C18 (2.1×50 mm) 1.7 μm; mobile phase A: H2O+0.02% FA; mobile phase B: ACN+0.02% FA eluting with a gradient of 2% B to 98% B over 4 min; flow rate of 1 ml/min, temperature of 55° C. t(R) isomer 1 is 3.3 min (22 mg, 20%). t(R) isomer 2 is 4.7 min (23 mg, 21%). ES/MS (m/z) 454 (M+H).
The following compounds in Table 21 are chirally separated essentially as described for 5-amino-1-isopropyl-3-[6-[2-[[3-(1,1-dimethylpropyl)isoxazol-5-yl]amino]-1-methyl-2-oxo-ethyl]-3-pyridyl]pyrazole-4-carboxamide, Isomer 1 and Isomer 2 adjusting the conditions as appropriate. The title compounds can be triturated with isopropyl ether and dried under vacuum at about 45° C. for 14 hrs to give white solids.
2-[4-(5-Amino-4-cyano-1-isopropyl-pyrazol-3-yl)phenyl]-N-[3-(3-bicyclo[1.1.1]pentanylmethyl)isoxazol-5-yl]propanamide, Isomer 1 (10 mg, 0.023 mmol) and platinate(2-), tris(dimethylphosphinito-P)hydro-, dihydrogen (Parkins catalyst, CAS #173416-05-2) (10 mg, 0.023 mmol) are stirred in EtOH (0.2 ml) and H2O (0.2 ml) at 70° C. for 90 min. The reaction mixture is filtered through diatomaceous earth and concentrated. The residue is purified by C18 HPLC eluting with H2O:ACN (5-95%) with 0.1% TFA. The free base of the desired product is formed by eluting the material through a cartridge of carbonate resin to give the title compound (4.3 mg, 39%). ES/MS (m/z) 463.2 (M+H) 99% ee, chiral purity determination: YMA Chiral Cellulose-SB column, 4.6×100 mm, 3 μm eluting with 70/30 hexanes (0.1% ethylenediamine)/IPA 1 ml/min, t(R) 3.78.
The following compounds in Table 22 are prepared essentially as described for 5-amino-3-[4-[2-[[3-(3-bicyclo[1.1.1]pentanylmethyl)isoxazol-5-yl]amino]-1-methyl-2-oxo-ethyl]phenyl]-1-isopropyl-pyrazole-4-carboxamide, Isomer 1 using the appropriate reagents, adjusting reaction time to determine completion of the reaction and using appropriate chromatography conditions for purification if needed. Temperature can vary from about 60 to 80° C. Further Parkin's catalyst can be used to push the reaction to completion if needed.
981
While only certain representative compounds, materials, and method steps disclosed herein are specifically described, other combinations of the compounds, materials, and method steps also are intended to fall within the scope of the appended claims, even if not specifically recited. Thus, a combination of steps, elements, components, or constituents may be explicitly mentioned herein; however, other combinations of steps, elements, components, and constituents are included, even though not explicitly stated. The term “comprising”, and variations thereof as used herein is used synonymously with the term “including” and variations thereof and are open, non-limiting terms. Although the terms “comprising” and “including” have been used herein to describe various embodiments, the terms “consisting essentially of” and “consisting of” can be used in place of “comprising” and “including” to provide for more specific embodiments of the invention and are also disclosed.
The following assays demonstrate that the compounds described herein are RET kinase inhibitors.
Assay A: RET Enzyme Assay
Compounds of formulas I, II, or III are screened for their ability to inhibit wildtype, V804M, and G810S mutant RET kinase using CisBio's HTRF® KinEASE™TK assay technology. N-terminal GST tagged recombinant human RET cytoplasmic domain (aa 658-end) from Eurofins (T25 nM RET; Catalog No. 14-570M) or N-terminal GST tagged recombinant human V804M mutant RET cytoplasmic domain (aa 658-end) from Millipore (1.25 nM enzyme; Catalog No. 14-760) or N-Terminal GST-tagged recombinant human G810S (aa-658-end) (1.25 nM Enzyme; produced in insect cells) is incubated with 62.5 nM TK-substrate biotin (CisBio, part of Catalog No. 62TK0PEC) and 1 mM ATP along with test compound (0.4% final DMSO in the assay) in a 1× Cisbio enzymatic buffer consisting of 1 nM DTT, 5 mM MgCl2, 0.04% BSA and 0.05% Tween20 in a volume of 10 μL. Compounds are typically prepared in a threefold serial dilution in DMSO and added to the assay to give the appropriate final concentration. After a 40-60 min (40 min for V804M, 60 min for WT and G810S) incubation at 22° C., the reaction is quenched by adding quench solution (10 μL) containing 7.8 nM Streptavidine-XL665 and 0.5×TK-ab-Cryptate in HTRF detection buffer (all from CisBio, part of Cat. No. 62TK0PEC). After a 60-80 min incubation (60 minutes for WT, 80 minutes for V804M and G810S) at 22° C., the extent of reaction is determined using a PHERastar plate reader via HTRF detection at excitation/emission 337/665 nm. Percent of inhibition is calculated with 0% inhibition referring to control conditions containing no compound (0.4% DMSO only) and 100% inhibition represented by conditions containing no enzyme. The % inhibition values are fit to a 4 parameter logistic curve, and the determined IC50 value is defined as the estimated concentration of inhibitor at the inflexion point of the fitted curve. The compounds of Examples 1, 15, 17, 35, 45, 52, 64, 66, 68, 70, 76, 80, 81, 84, 90, 94, and 98 all exhibited IC50 values of less than 100 nM for each of wildtype, V804M, and G810S mutant RET kinase in these assays. All of the compounds in Table A have IC50 values of less than 700 nm in the wildtype, V804M, and G810S mutant RET kinase assays.
Compounds of formulas (I), (II), and (III) are screened for their ability to inhibit the intracellular autophosphorylation of RET at tyrosine 1062 as detected by In-Cell Western. HEK293 cells containing a doxycycline-inducible plasmid for inducible expression of KIF5B-RET WT and RET mutant forms V804M and G810S are seeded at 25,000 cells/well into black poly-D-lysine pre-coated 384-well plates (Corning, Catalog No. 356697). Expression of KIF5B-RET is induced with doxycycline at 1 μg/mL and cells are incubated at 37° C. overnight. Compounds are prepared in a threefold serial dilution in DMSO before further diluting 1:100 in media prior to the addition to the cells (0.1% final DMSO concentration). Compound treatment is performed for 1 hr at 37° C. followed by fixation of cells with 4% formaldehyde for 20 min at RT and cell permeabilisation with ice-cold MeOH for 10 min at RT. Cells are incubated with Intercept® blocking buffer (Li—COR, Catalogue No. 927-70010) for 1 hr at RT. Incubation with primary antibodies against human phospho-RET (Y1062) (R&D, Catalogue No. AF5009, 1/250 dilution) and human glyceraldehyde-3-phosphate dehydrogenase (clone 6C5, Merck, Catalog No. MAB374, 1/1000 dilution) are performed overnight at 4° C. Incubation with secondary antibodies IRDye® 800CW goat anti-rabbit IgG (Li—COR, Catalogue No. 926-32211, 1/1000 dilution) and IRDye® 680CW goat anti-mouse IgG (Li—COR, Catalogue No. 926-68070, 1/1000 dilution) are performed for 1 hr at RT. All antibody dilutions are done in Intercept® blocking buffer containing 0.05% Tween20. After washing cells with PBS-T (Cell Signaling technology, Catalogue No. 9809), the images are acquired on a Li—COR Odyssey LCx at 700 and 800 nm. Percent of DMSO control is calculated with 100% signal referring to control conditions containing no compound (0.4% DMSO only) and 0% signal represented by conditions containing control compound. The % of DMSO control values are fit to a 4 parameter logistic curve, and the determined EC50 value is defined as the estimated concentration of inhibitor at the inflexion point of the fitted curve. The compounds of Examples 1, 15, 17, 31, 33, 35, 45, 52, 64, 66, 68, 70, 76, 80, 81, 84, 90, 94, and 98 all inhibited the intracellular autophosphorylation of RET at tyrosine 1062 with EC50 values of less than 100 nM in each of wildtype, V804M, and G810S RET mutant cells in these assays. All of the compounds in Table B have IC50 values of less than 700 nm in the wildtype, V804M, and G810S mutant RET kinase assays.
| Number | Name | Date | Kind |
|---|---|---|---|
| 10183928 | Kim | Jan 2019 | B2 |
| 20170267661 | Kim et al. | Sep 2017 | A1 |
| Number | Date | Country |
|---|---|---|
| 2014141187 | Sep 2014 | WO |
| 2017145050 | Aug 2017 | WO |
| 2020035065 | Feb 2020 | WO |
| Entry |
|---|
| International Search Report and Written Opinion in International Application No. PCT/US2021/028836, dated Jul. 2, 2021, 6 pages. |
| Number | Date | Country | |
|---|---|---|---|
| 20210363140 A1 | Nov 2021 | US |
| Number | Date | Country | |
|---|---|---|---|
| 63015933 | Apr 2020 | US |
