Patent Application
20230119894
The present invention relates to a medicament for use in treating or preventing diabetes, obesity, or diabetic complications, wherein an SGLT1 inhibitor is used in combination with at least one drug selected from SGLT2 inhibitors and DPP4 inhibitors; and a method of treating or preventing diabetes, obesity, or diabetic complications, comprising administering an SGLT1 inhibitor and at least one drug selected from SGLT2 inhibitors and DPP4 inhibitors.
SGLT1 1 is known as one of subtypes of SGLT (Na+-Glucose Cotransporters) to contribute to a great portion of absorption of glucose and galactose in the small intestine. It is reported that human SGLT1-deficient patients cause glucose-galactose malabsorption. Furthermore, it is confirmed that the expression of SGLT1 in the small intestine increases in diabetic patients and it is thought that increased sugar absorption in diabetic patients is caused by the high expression of SGLT1 in the small intestine.
Based on the knowledge, an SGLT1 inhibitor is expected to normalize the blood glucose level by blocking glucose absorption in the small intestine. An SGLT1 inhibitor is, therefore, considered to be effective against diabetes and diabetic complications associated with hyperglycemia. It is also considered to be effective against obesity by inhibiting the inflow of glucose into the body (Non Patent Literatures 1 and 2).
Voglibose, a generic name, is a drug approved for manufacturing and marketing under the Japan Pharmaceutical Affairs Act Article 14 (Approval number: 21600AMZ00368). Voglibose improves excess blood glucose after eating by inhibiting disaccharidase, α-glucosidase, that degrades disaccharides existing in the intestinal mucosa into monosaccharides and inhibiting or delaying the digestion and absorption of carbohydrate in the intestinal tract. Such a pharmacological effect is known to be effective against delayed onset of type 2 diabetes in impaired glucose tolerance.
Based on the knowledge, inhibition of sugar absorption through small intestine with an SGLT1 inhibitor and thereby improvement of excess blood glucose after eating is thought to be effective against delayed onset of type 2 diabetes in impaired glucose tolerance.
Diabetes is caused by elevated blood glucose level due to the deficient insulin action and the persistent elevated blood glucose may cause diabetic complication (e.g., retinopathy, nephropathy, and neuropathy, which are all known as microangiopathy; and cerebrovascular disease, ischemic heart disease, and membrum-inferius arteriosclerosis obliterans, which are all known as macroangiopathy). Other diseases associated with elevated blood glucose level include obesity.
Diabetes is classified as type 1 and type 2 diabetes. Type 1 diabetes is considered to be developed due to the deficient insulin action caused by destruction of pancreatic β cells that secretes insulin, whereas type 2 diabetes is considered to be developed due to environmental factors, such as overeating, insufficient exercise, obesity, and stress, and aging in addition to multiple genetic factors including a decrease in insulin secretion and insulin resistance. Diabetes is diagnosed using three types, such as the normal, borderline, and diabetic types, classified on the basis of the blood glucose level. When any one of the following (1) to (4):
(1) 126 mg/dL or more of blood glucose level in the morning fasting;
(2) 200 mg/dL or more of two-hour value in 75 g OGTT (oral glucose tolerance test);
(3) 200 mg/dL or more of casual blood glucose level; or
(4) 6.5% or more of HbA1cg
is identified, then the subject is determined as the diabetic type and diagnosed as diabetes or suspected diabetes (Non Patent Literature 3).
OGTT used in the above (2) is one of the methods for diagnosing diabetes. In general, a human subject is diagnosed as diabetes in the case where the subject is determined as 200 mg/dL or more of the blood glucose level in a certain period of time after administration of a solution comprising 75 g of glucose after fasting (Non Patent Literature 3). OGTT is, therefore, an index of diabetes diagnosis, and a compound that can reduce blood glucose levels of glucose-loaded subjects in OGTT is considered to be effective against diabetes.
SGLT2 is one of subtypes of SGLT and is localized mainly in the proximal convoluted tubules of the kidney. SGLT2 has a function to intracellularly reuptake glucose at the proximal convoluted tubules. It is thought that an SGLT2 inhibitor inhibits reuptake of glucose from the urine to increase the excretion amount of sugar in the urine so as to reduce the blood glucose level.
A typical SGLT2 inhibitor includes dapagliflozin clinically used as an anti-diabetic agent. It is reported that administration of dapagliflozin to diabetic model animals and diabetic patients increases the excretion amount of glucose in the urine and ameliorates hyperglycemia.
Dipeptidyl peptidase-4 (DPP4) decomposes insulin-secretion stimulating hormones dependent on the glucose level, glucagon-like peptide-1 (GLP-1) and glucose-dependent insulin-secretion stimulating polypeptide (GIP), and inactivates these. It is thus thought that DPP4 inhibitors inhibit decomposition of GLP-1 and GIP, so as to enhance insulin secretion depending on the glucose level and to reduce the blood glucose level.
A typical DPP4 inhibitor includes sitagliptin clinically used as an anti-diabetic agent. It is reported that administrations of sitagliptin to diabetic model animals and diabetic patients increase the blood levels of GLP-1 and GIP and ameliorate hyperglycemia.
Provided are a medicament for use in treating or preventing diabetes, obesity, or diabetic complications, wherein an SGLT1 inhibitor is used in combination with at least one drug selected from SGLT2 inhibitors and DPP4 inhibitors, and a method of treating or preventing diabetes, obesity, or diabetic complications, comprising administering an SGLT1 inhibitor and at least one drug selected from SGLT2 inhibitors and DPP4 inhibitors.
Certain embodiments are illustrated as follows.
A medicament for use in treating or preventing diabetes, obesity, or diabetic complications, comprising an SGLT1 inhibitor, wherein the SGLT1 inhibitor is used in combination with at least one drug selected from SGLT2 inhibitors and DPP4 inhibitors.
A medicament for use in treating or preventing diabetes, obesity, or diabetic complications, comprising at least one drug selected from SGLT2 inhibitors and DPP4 inhibitors, wherein the at least one drug is used in combination with an SGLT1 inhibitor.
A medicament for use in treating or preventing diabetes, obesity, or diabetic complications, comprising a compound of Formula [I]:
or a pharmaceutically acceptable salt thereof,
wherein R1 is hydrogen or halogen;
R2 is C1-6 alkyl or halo-C1-6 alkyl;
R3 is
(1) C1-6 alkyl,
(2) halo-C1-6 alkyl,
(3) pyridyl substituted with R3A, or
(4) pyrazinyl, pyrimidinyl, or pyridazinyl, which may be optionally substituted with R3B;
R3A is cyano, halogen, or halo-C1-3 alkyl;
R3B is halogen, hydroxy, C1-3 alkyl, halo-C1-3 alkyl, C1-3 alkoxy, or —N(R4)(R5); and
R4 and R5 are each independently hydrogen or C1-3 alkyl, wherein the compound of Formula [I], or a pharmaceutically acceptable salt thereof, is used in combination with at least one drug selected from SGLT2 inhibitors and DPP4 inhibitors.
A medicament for use in treating or preventing diabetes, obesity, or diabetic complications, comprising at least one drug selected from SGLT2 inhibitors and DPP4 inhibitors, wherein the at least one drug is used in combination with a compound of Formula [I]:
or a pharmaceutically acceptable salt thereof,
wherein R1 is hydrogen or halogen;
R2 is C1-6 alkyl or halo-C1-6 alkyl;
R3 is
(1) C1-6 alkyl,
(2) halo-C1-6 alkyl,
(3) pyridyl substituted with R3A, or
(4) pyrazinyl, pyrimidinyl, or pyridazinyl, which may be optionally substituted with R3B;
R3A is cyano, halogen, or halo-C1-3 alkyl;
R3B is halogen, hydroxy, C1-3 alkyl, halo-C1-3 alkyl, C1-3 alkoxy, or —N(R4)(R5); and
R4 and R5 are each independently hydrogen or C1-3 alkyl.
A medicament for use in treating or preventing diabetes, obesity, or diabetic complications, comprising a compound of Formula [I]:
or a pharmaceutically acceptable salt thereof,
wherein R1 is hydrogen or halogen;
R2 is C1-6 alkyl or halo-C1-6 alkyl;
R3 is
(1) C1-6 alkyl,
(2) halo-C1-6 alkyl,
(3) pyridyl substituted with R3A, or
(4) pyrazinyl, pyrimidinyl, or pyridazinyl, which may be optionally substituted with R3B;
R3A is cyano, halogen, or halo-C1-3 alkyl;
R3B is halogen, hydroxy, C1-3 alkyl, halo-C1-3 alkyl, C1-3 alkoxy, or —N(R4)(R5); and
R4 and R5 are each independently hydrogen or C1-3 alkyl, wherein the medicament is administered to a subject who is under treatment with at least one drug selected from SGLT2 inhibitors and DPP4 inhibitors.
A medicament for use in treating or preventing diabetes, obesity, or diabetic complications, comprising at least one drug selected from SGLT2 inhibitors and DPP4 inhibitors, wherein the medicament is administered to a subject who is under treatment with a compound of Formula [I]:
or a pharmaceutically acceptable salt thereof,
wherein R1 is hydrogen or halogen;
R2 is C1-6 alkyl or halo-C1-6 alkyl;
R3 is
(1) C1-6 alkyl,
(2) halo-C1-6 alkyl,
(3) pyridyl substituted with R3A, or
(4) pyrazinyl, pyrimidinyl, or pyridazinyl, which may be optionally substituted with R3B;
R3A is cyano, halogen, or halo-C1-3 alkyl;
R3B is halogen, hydroxy, C1-3 alkyl, halo-C1-3 alkyl, C1-3 alkoxy, or —N(R4)(R5); and
R4 and R5 are each independently hydrogen or C1-3 alkyl.
The medicament according to any one of Items 1 to 6, wherein the SGLT1 inhibitor or the compound of Formula [I], or a pharmaceutically acceptable salt thereof, is any one of compounds of Formulae [II] to [V]:
or a pharmaceutically acceptable salt thereof.
The medicament according to any one of Items 1 to 6, wherein the SGLT1 inhibitor or the compound of Formula [I], or a pharmaceutically acceptable salt thereof, is a compound of Formula [II]:
or a pharmaceutically acceptable salt thereof.
The medicament according to any one of Items 1 to 6, wherein the SGLT2 inhibitor is dapagliflozin.
The medicament according to any one of Items 1 to 6, wherein the DPP4 inhibitor is sitagliptin.
The medicament according to any one of Items 1 to 6, wherein the diabetes is type 2 diabetes.
The medicament according to Item 5 or 6, wherein the subject is human.
A method of treating or preventing diabetes, obesity, or diabetic complications, comprising administering a therapeutically effective amount of an SGLT1 inhibitor and a therapeutically effective amount of at least one drug selected from SGLT2 inhibitors and DPP4 inhibitors to a subject.
An SGLT1 inhibitor for use in treating or preventing diabetes, obesity, or diabetic complications, wherein the SGLT1 inhibitor is used in combination with at least one drug selected from SGLT2 inhibitors and DPP4 inhibitors.
At least one drug selected from SGLT2 inhibitors and DPP4 inhibitors for use in treating or preventing diabetes, obesity, or diabetic complications, wherein the at least one drug is used in combination with an SGLT1 inhibitor.
Use of an SGLT1 inhibitor in the manufacture of a medicament for use in treating or preventing diabetes, obesity, or diabetic complications, wherein the medicament is used in combination with at least one drug selected from SGLT2 inhibitors and DPP4 inhibitors.
Use of at least one drug selected from SGLT2 inhibitors and DPP4 inhibitors in the manufacture of a medicament for use in treating or preventing diabetes, obesity, or diabetic complications, wherein the medicament is used in combination with an SGLT1 inhibitor.
A pharmaceutical composition for use in treating or preventing diabetes, obesity, or diabetic complications, comprising an SGLT1 inhibitor and at least one drug selected from SGLT2 inhibitors and DPP4 inhibitors.
A pharmaceutical composition for use in treating or preventing diabetes, obesity, or diabetic complications, comprising a compound of Formula [I]:
or a pharmaceutically acceptable salt thereof,
wherein R1 is hydrogen or halogen;
R2 is C1-6 alkyl or halo-C1-6 alkyl;
R3 is
(1) C1-6 alkyl,
(2) halo-C1-6 alkyl,
(3) pyridyl substituted with R3A, or
(4) pyrazinyl, pyrimidinyl, or pyridazinyl, which may be optionally substituted with R3B;
R3A is cyano, halogen, or halo-C1-3 alkyl;
R3B is halogen, hydroxy, C1-3 alkyl, halo-C1-3 alkyl, C1-3 alkoxy, or —N(R4)(R5); and
R4 and R5 are each independently hydrogen or C1-3 alkyl, and at least one drug selected from SGLT2 inhibitors and DPP4 inhibitors.
The composition according to Item 18 or 19, wherein the SGLT1 inhibitor or the compound of Formula [I], or a pharmaceutically acceptable salt thereof, is any one of compounds of Formulae [II] to [V]:
or a pharmaceutically acceptable salt thereof.
The composition according to Item 18 or 19, wherein the SGLT1 inhibitor or the compound of Formula [I], or a pharmaceutically acceptable salt thereof, is a compound of Formula [II]:
or a pharmaceutically acceptable salt thereof.
The SGLT1 inhibitor used herein is any substance that inhibits SGLT1, and includes low-molecular compounds, nucleic acids, polypeptides, proteins, antibodies, and vaccines. In one embodiment, the SGLT1 inhibitor is a substance that may normalize the blood glucose level by inhibiting sugar absorption from organs such as the small intestine and the myocardium. In another embodiment, the SGLT1 inhibitor is a substance that may suppress a rapid rise of the glucose concentration in plasma right after, for example, 0 to 30 minutes after, the glucose load in the OGTT, and then maintain the suppressed glucose concentration in plasma nearly equal thereto or less. In still another embodiment, the SGLT1 inhibitor is a substance that may increase the active GLP-1 concentration in plasma after the glucose load in the OGTT. In still another embodiment, the SGLT1 inhibitor is a compound of Formula [I]:
or a pharmaceutically acceptable salt thereof,
wherein each symbol has the same meaning as defined above. In still another embodiment, the SGLT1 inhibitor is a substance, a metabolite of which does not show mutagenicity. The substance herein that does not show mutagenicity means, for example, a substance that does not have potential to induce reverse mutations under, for example, the condition of Test Example 4 mentioned below. In still another embodiment, the SGLT1 inhibitor is a human SGLT1 inhibitor.
A double wave line of the following:
in a partial structure herein is a binding site of the structure.
The term “halogen” used herein includes, for example, fluorine, chlorine, bromine, and iodine.
The term “C1-3 alkyl” used herein means a straight- or branched-chain saturated hydrocarbon group having 1 to 3 carbon atoms. The term “C1-3 alkyl” includes methyl, ethyl, n-propyl, and isopropyl.
The term “C1-6 alkyl” used herein means a straight- or branched-chain saturated hydrocarbon group having 1 to 6 carbon atoms. The term “C1-6 alkyl” includes, for example, methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl, tert-butyl, n-pentyl, isopentyl, and n-hexyl.
The term “halo-C1-3 alkyl” used herein means the above mentioned “C1-3 alkyl” that is substituted with 1 to 5 halogen atoms independently selected from the group of the above mentioned “halogen”. The term “halo-C1-3 alkyl” includes, for example, monofluoromethyl, difluoromethyl, trifluoromethyl, 2-fluoroethyl, 2-chloroethyl, 2-bromoethyl, 1,1-difluoroethyl, 2,2,2-trifluoroethyl, pentafluoroethyl, 3-fluoropropyl, 3-chloropropyl, 1,1-difluoropropyl, and 3,3,3-trifluoropropyl.
The term “fluoro-C1-3 alkyl” used herein means the above mentioned “C1-3 alkyl” that is substituted with 1 to 5 fluorine atoms. The term “fluoro-C1-3 alkyl” includes, for example, monofluoromethyl, difluoromethyl, trifluoromethyl, 2-fluoroethyl, 1,1-difluoroethyl, 2,2,2-trifluoroethyl, pentafluoroethyl, 3-fluoropropyl, 1,1-difluoropropyl, and 3,3,3-trifluoropropyl.
The term “halo-C1-6 alkyl” used herein means the above mentioned “C1-6 alkyl” that is substituted with 1 to 5 halogen atoms independently selected from the group of the above mentioned “halogen”. The term “halo-C1-6 alkyl” includes, for example, monofluoromethyl, difluoromethyl, trifluoromethyl, 2-fluoroethyl, 2-chloroethyl, 2-bromoethyl, 1,1-difluoroethyl, 2,2,2-trifluoroethyl, pentafluoroethyl, 3-fluoropropyl, 3-chloropropyl, 1,1-difluoropropyl, 3,3,3-trifluoropropyl, 4,4,4-trifluorobutyl, 5,5,5-trifluoropentyl, and 6,6,6-trifluorohexyl.
The term “fluoro-C1-6 alkyl” used herein means the above mentioned “C1-6 alkyl” that is substituted with 1 to 5 fluorine atoms. The term “fluoro-C1-6 alkyl” includes, for example, monofluoromethyl, difluoromethyl, trifluoromethyl, 2-fluoroethyl, 1,1-difluoroethyl, 2,2,2-trifluoroethyl, pentafluoroethyl, 3-fluoropropyl, 1,1-difluoropropyl, 3,3,3-trifluoropropyl, 4,4,4-trifluorobutyl, 5,5,5-trifluoropentyl, and 6,6,6-trifluorohexyl.
The term “C1-3 alkoxy” used herein means a group wherein the above mentioned “C1-3 alkyl” binds to an oxygen atom. The term “C1-3 alkoxy” includes methoxy, ethoxy, n-propoxy, and isopropoxy.
The term “pyridyl” used herein means any one of the following formulae.
The term “pyrazinyl” used herein means the following formula.
The term “pyrimidinyl” used herein means any one of the following formulae.
The term “pyridazinyl” used herein means any one of the following formulae.
The term “substitute” used herein includes any chemically acceptable substitution. For example, the term “pyridyl substituted with R3A” used herein means any one of the following formulae.
Each substituent of a compound of Formula [I] includes embodiments illustrated as below for each substituent, and a compound of Formula [I] includes any combinations of these embodiments for each substituent.
In one embodiment, R1 is halogen. In another embodiment, R1 is fluorine.
In one embodiment, R2 is C1-6 alkyl or fluoro-C1-6 alkyl. In another embodiment, R2 is C1-6 alkyl. In still another embodiment, R2 is fluoro-C1-3 alkyl.
In one embodiment, R3 is
(1) halo-C1-6 alkyl,
(2) pyridyl substituted with R3A, or
(3) pyrazinyl or pyrimidinyl, which may be optionally substituted with R3B.
In another embodiment, R3 is selected from the group consisting of halo-C1-6 alkyl and groups of Formulae [H1] to [H14].
In still another embodiment, R3 is halo-C1-6 alkyl, or a group of Formula [H2] or [H8].
In one embodiment, R3A is halogen or halo-C1-3 alkyl. In another embodiment, R3A is fluorine or fluoro-C1-3 alkyl.
In one embodiment, R3B is halogen or halo-C1-3 alkyl. In another embodiment, R3B is fluoro-C1-3 alkyl.
In one embodiment, R4 and R5 are each independently C1-3 alkyl.
In one embodiment, a compound of Formula [I] is a compound of Formula [II] or [III]:
In another embodiment, a compound of Formula [I] is a compound of Formula [II]. In still another embodiment, a compound of Formula [I] is a compound of Formula [III] monohydrate, i.e., a compound of Formula [VI]:
The term “pharmaceutically acceptable salt” includes any salts known in the art that are not associated with excessive toxicity. Such a pharmaceutically acceptable salt includes, specifically, salts with inorganic acids, salts with organic acids, salts with inorganic bases, and salts with organic bases. Various forms of pharmaceutically acceptable salts are well known in the art and are described in, for example, the following references:
A compound of Formula [I] may be reacted with an inorganic acid, organic acid, inorganic base, or organic base according to methods known per se to give each corresponding pharmaceutically acceptable salt thereof.
Such a salt with inorganic acid includes a salt with hydrofluoric acid, hydrochloric acid, hydrobromic acid, hydroiodic acid, nitric acid, phosphoric acid, and sulfuric acid. Such a salt preferably includes a salt with hydrochloric acid, nitric acid, sulfuric acid, phosphoric acid, and hydrobromic acid.
Such a salt with organic acid includes a salt with acetic acid, adipic acid, alginic acid, 4-aminosalicylic acid, anhydromethylenecitric acid, benzoic acid, benzenesulfonic acid, calcium edetate, camphor acid, camphor-10-sulfonic acid, carbonic acid, citric acid, edetic acid, ethane-1,2-disulfonic acid, dodecylsulfuric acid, ethanesulfonic acid, fumaric acid, glucoheptonic acid, gluconic acid, glucuronic acid, glucoheptonic acid, glycollylarsanilic acid, hexylresorcinol acid, hydroxynaphthoic acid, 2-hydroxy-1-ethanesulfonic acid, lactic acid, lactobionic acid, malic acid, maleic acid, mandelic acid, methanesulfonic acid, methylsulfuric acid, methylnitric acid, methylenebis(salicylic acid), galactaric acid, naphthalene-2-sulfonic acid, 2-naphthoic acid, 1,5-naphthalenedisulfonic acid, oleic acid, oxalic acid, pamoic acid, pantothenic acid, pectic acid, picric acid, propionic acid, polygalacturonic acid, salicylic acid, stearic acid, succinic acid, tannic acid, tartaric acid, teoclic acid, thiocyanic acid, trifluoroacetic acid, p-toluenesulfonic acid, undecanoic acid, aspartic acid, and glutamic acid. Such a salt preferably includes a salt with oxalic acid, maleic acid, citric acid, fumaric acid, lactic acid, malic acid, succinic acid, tartaric acid, acetic acid, trifluoroacetic acid, benzoic acid, glucuronic acid, oleic acid, pamoic acid, methanesulfonic acid, benzenesulfonic acid, p-toluenesulfonic acid, and 2-hydroxy-1-ethanesulfonic acid.
Such a salt with inorganic base includes a salt with lithium, sodium, potassium, magnesium, calcium, barium, aluminum, zinc, bismuth, and ammoinum. Such a salt preferably includes a salt with sodium, potassium, calcium, magnesium, and zinc.
Such a salt with organic base includes a salt with arecoline, betaine, choline, clemizole, ethylenediamine, N-methylglucamine, N-benzylphenethylamine, tris(hydroxymethyl)methylamine, arginine, and lysine. Such a salt preferably includes a salt with tris(hydroxymethyl)methylamine, N-methylglucamine, and lysine.
Active ingredients of an SGLT1 inhibitor, e.g., a compound of Formula [I] or a pharmaceutically acceptable salt thereof, an SGLT2 inhibitor, and a DPP4 inhibitor may exist in their solvate forms. The term “solvate” means a compound where a solvent molecule is coordinated with, for example, a compound of Formula [I] or a pharmaceutically acceptable salt thereof. The solvate may be a pharmaceutically acceptable solvate; and includes, for example, a hydrate, an ethanolate, and a dimethylsulfoxide solvate of a compound of Formula [I] or a pharmaceutically acceptable salt thereof. The solvate specifically includes a hemihydrate, monohydrate, dihydrate, and monoethanolate of a compound of Formula [I]; and a monohydrate of sodium salt of a compound of Formula [I] and a 2/3 ethanolate of dihydrochloride salt thereof. These solvates may be obtained according to any of the known methods. For example, a compound of Formula [III] may exist as its monohydrate as seen in the following Formula [VI].
A compound of Formula [I] may be labelled with an isotope such as 2H, 3H, 14C, and 35S.
A compound of Formula [I] or a pharmaceutically acceptable salt thereof is preferably a compound of Formula [I] or a pharmaceutically acceptable salt thereof that is substantively purified, and more preferably a compound of Formula [I] or a pharmaceutically acceptable salt thereof that is purified into a purity of 80% or more.
Inhibiting SGLT1 means that the function of SGLT1 is inhibited so as to disappear or reduce its activity; and, for example, this means that the function of SGLT1 is inhibited on the basis of the following Test Example 1. Preferably, inhibiting SGLT1 means inhibiting human SGLT1. The inhibition of the function of SGLT1, or the disappearance or reduction of its activity is preferably carried out in human clinical indications.
The SGLT2 inhibitor herein may be any substance that inhibits SGLT2, and includes substances such as small molecule compounds, nucleic acids, polypeptides, proteins, antibodies, and vaccines. In one embodiment, an SGLT2 inhibitor is a substance with a function to inhibit reuptake of glucose from the urine to increase the excretion amount of sugar in the urine so that the blood glucose level can be reduced.
Inhibiting SGLT2 means that the function of SGLT2 is inhibited so as to disappear or reduce its activity. Preferably, inhibiting SGLT2 means inhibiting human SGLT2. The inhibition of the function of SGLT2, or the disappearance or reduction of its activity is preferably carried out in human clinical indications.
The SGLT2 inhibitor herein includes, for example, glycosides and salts thereof and solvates thereof. The glycosides herein are those compounds wherein sugars or sugar derivatives glycosidically bind to aglycone moieties (e.g., through a C-glycosidic bond or O-glycosidic bond) and the sugars or sugar derivatives are those having the following structure:
wherein Y is O or S and a glycosidic bond is formed on the carbon atom at the 1-position.
The SGLT2 inhibitor herein includes, for example, the following compounds. For the convenience, trivial names are used herein.
The DPP4 inhibitor herein may be any substance that inhibits DPP4, and includes substances such as small molecule compounds, nucleic acids, polypeptides, proteins, antibodies, and vaccines. In one embodiment, a DPP4 inhibitor is a substance with a function to inhibit decomposition of GLP-1 and GIP so that glucose-level-dependent insulin secretion can be enhanced and the blood glucose level can be reduced.
Inhibiting DPP4 means that the function of DPP4 is inhibited so as to disappear or reduce its activity. Preferably, inhibiting DPP4 means inhibiting human DPP4. The inhibition of the function of DPP4, or the disappearance or reduction of its activity is preferably carried out in human clinical indications.
The DPP4 inhibitor herein includes, for example, gliptins having at least one amide or sulfonamide group and salts thereof and solvates thereof.
The DPP4 inhibitor herein includes, for example, the following compounds. For the convenience, trivial names are used herein.
An SGLT1 inhibitor, e.g., a compound of Formula [I] or a pharmaceutically acceptable salt thereof, an SGLT2 inhibitor, and a DPP4 inhibitor have an SGLT1 inhibitory activity, an SGLT2 inhibitory activity, and a DPP4 inhibitory activity, respectively, and may be useful for treating and/or preventing various diseases or conditions that are expected to be alleviated with adjustment of these activities or that may be caused by elevated blood glucose levels due to sugar absorption in the body, e.g., diabetes such as type 1 diabetes and type 2 diabetes, obesity, and/or diabetic complications such as retinopathy, nephropathy, and neuropathy, which are known as microangiopathy, and cerebrovascular disease, ischemic heart disease, and membrum-inferius arteriosclerosis obliterans, which are known as macroangiopathy. In one embodiment, the various diseases or conditions are diabetes, obesity, or diabetic complications. In another embodiment, the various diseases or conditions are diabetes. In still another embodiment, the various diseases or conditions are type 1 diabetes. In still another embodiment, the various diseases or conditions are type 2 diabetes.
The phrase “used in combination (or combination use)” used herein means administering an SGLT1 inhibitor, e.g., a compound of Formula [I] or a pharmaceutically acceptable salt thereof, and at least one drug selected from SGLT2 inhibitors and DPP4 inhibitors in any order to a subject. Each drug has each particular mode of action, and combination use of these drugs may provide an additive or synergistic therapeutic or preventive effect against at least one disease of the various diseases or conditions. In one embodiment, combination use may significantly suppress a rapid rise of the glucose concentration in plasma right after, for example, 0 to 30 minutes after, the glucose load in the OGTT, and then maintain the suppressed glucose concentration in plasma nearly equal thereto or less. In another embodiment, combination use may significantly increase the active GLP-1 concentration in plasma right after, for example, 0 to 30 minutes after, the glucose load in the OGTT, and then maintain the increased active GLP-1 concentration in plasma nearly equal thereto. In still another embodiment, combination use where multiple drugs with different modes of action are used may reduce the dosage amount of each drug compared to the case where each drug is used alone, and may reduce side effects specific to each drug. In one embodiment, a first drug and a second drug and/or a third drug selected from an SGLT1 inhibitor and an SGLT2 inhibitor and a DPP4 inhibitor may be administered to a subject concurrently, sequentially, or with a certain interval, e.g., within 30 minutes, within one hour, within two hours, and within four hours, together or separately in any order. The second drug and/or the third drug may be administered while a therapeutically effective amount of the active ingredient comprised in the first drug administered first exists in the body of a subject when these drugs are administered to the subject. In another embodiment, an SGLT1 inhibitor may be administered to a subject in a single combined formulation wherein the SGLT1 inhibitor is comprised in combination with at least one drug selected from SGLT2 inhibitors and DPP4 inhibitors. The ratios of these drugs to be administered or blended may be optionally selected depending on subjects to be administered, administration routes, subject diseases, symptoms, severity of diseases, and combinations thereof. For example, when the subjects to be administered are a human, 0.01 to 1000 parts by weight of at least one drug selected from SGLT2 inhibitors and DPP4 inhibitors may be used for one part by weight of an SGLT1 inhibitor.
In one embodiment, combination use of an SGLT1 inhibitor with an SGLT2 inhibitor includes use of a compound of Formula [I] in combination with glycoside or a salt thereof or a solvate thereof.
In another embodiment, combination use of an SGLT1 inhibitor with an SGLT2 inhibitor includes use of a compound of Formula [II] in combination with glycoside or a salt thereof or a solvate thereof.
In one embodiment, combination use of an SGLT1 inhibitor with an SGLT2 inhibitor includes:
use of a compound of Formula [I] in combination with dapagliflozin,
use of a compound of Formula [I] in combination with ipragliflozin,
use of a compound of Formula [I] in combination with tofogliflozin,
use of a compound of Formula [I] in combination with empagliflozin,
use of a compound of Formula [I] in combination with canagliflozin, and
use of a compound of Formula [I] in combination with luseogliflozin.
In another embodiment, combination use of an SGLT1 inhibitor with an SGLT2 inhibitor includes:
use of a compound of Formula [II] in combination with dapagliflozin,
use of a compound of Formula [II] in combination with ipragliflozin,
use of a compound of Formula [II] in combination with tofogliflozin,
use of a compound of Formula [II] in combination with empagliflozin,
use of a compound of Formula [II] in combination with canagliflozin, and
use of a compound of Formula [II] in combination with luseogliflozin.
In one embodiment, combination use of an SGLT1 inhibitor with a DPP4 inhibitor includes use of a compound of Formula [I] in combination with gliptins having at least one amide group or sulfonamide group or salts thereof or solvates thereof.
In another embodiment, combination use of an SGLT1 inhibitor with a DPP4 inhibitor includes use of a compound of Formula [II] in combination with gliptins having at least one amide group or sulfonamide group or salts thereof or solvates thereof.
In one embodiment, combination use of an SGLT1 inhibitor with a DPP4 inhibitor includes:
use of a compound of Formula [I] in combination with sitagliptin,
use of a compound of Formula [I] in combination with saxagliptin,
use of a compound of Formula [I] in combination with vildagliptin,
use of a compound of Formula [I] in combination with linagliptin,
use of a compound of Formula [I] in combination with teneligliptin,
use of a compound of Formula [I] in combination with alogliptin,
use of a compound of Formula [I] in combination with anagliptin,
use of a compound of Formula [I] in combination with trelagliptin, and
use of a compound of Formula [I] in combination with omarigliptin.
In another embodiment, combination use of an SGLT1 inhibitor with a DPP4 inhibitor includes:
use of a compound of Formula [II] in combination with sitagliptin,
use of a compound of Formula [II] in combination with saxagliptin,
use of a compound of Formula [II] in combination with vildagliptin,
use of a compound of Formula [II] in combination with linagliptin,
use of a compound of Formula [II] in combination with teneligliptin,
use of a compound of Formula [II] in combination with alogliptin,
use of a compound of Formula [II] in combination with anagliptin,
use of a compound of Formula [II] in combination with trelagliptin, and
use of a compound of Formula [II] in combination with omarigliptin.
In one embodiment, a medicament for use in treating or preventing diabetes, obesity, or diabetic complications, comprising a compound of Formula [II]:
or a pharmaceutically acceptable salt thereof, wherein the compound of Formula [II], or a pharmaceutically acceptable salt thereof, is used in combination with at least one drug selected from dapagliflozin and sitagliptin is provided.
In another embodiment, a medicament for use in treating or preventing diabetes, obesity, or diabetic complications, comprising at least one drug selected from dapagliflozin and sitagliptin, wherein the at least one drug selected from dapagliflozin and sitagliptin is used in combination with a compound of Formula [II]:
or a pharmaceutically acceptable salt thereof, is provided.
In still another embodiment, a medicament for use in treating or preventing diabetes, comprising a compound of Formula [II]:
or a pharmaceutically acceptable salt thereof, wherein the compound of Formula [II], or a pharmaceutically acceptable salt thereof, is used in combination with at least one drug selected from dapagliflozin and sitagliptin is provided.
In still another embodiment, a medicament for use in treating or preventing diabetes, comprising at least one drug selected from dapagliflozin and sitagliptin, wherein the at least one drug selected from dapagliflozin and sitagliptin is used in combination with a compound of Formula [II]:
or a pharmaceutically acceptable salt thereof, is provided.
In still another embodiment, a medicament for use in treating or preventing type 2 diabetes, comprising a compound of Formula [II]:
or a pharmaceutically acceptable salt thereof, wherein the compound of Formula [II], or a pharmaceutically acceptable salt thereof, is used in combination with at least one drug selected from dapagliflozin and sitagliptin is provided.
In still another embodiment, a medicament for use in treating or preventing type 2 diabetes, comprising at least one drug selected from dapagliflozin and sitagliptin, wherein the at least one drug selected from dapagliflozin and sitagliptin is used in combination with a compound of Formula [II]:
or a pharmaceutically acceptable salt thereof, is provided.
In still another embodiment, a medicament for use in treating or preventing type 2 diabetes, comprising a compound of Formula [II]:
or a pharmaceutically acceptable salt thereof, wherein the compound of Formula [II], or a pharmaceutically acceptable salt thereof, is used in combination with dapagliflozin is provided.
In still another embodiment, a medicament for use in treating or preventing type 2 diabetes, comprising dapagliflozin, wherein dapagliflozin is used in combination with a compound of Formula [II]:
or a pharmaceutically acceptable salt thereof, is provided.
In still another embodiment, a medicament for use in treating or preventing type 2 diabetes, comprising a compound of Formula [II]:
or a pharmaceutically acceptable salt thereof, wherein the compound of Formula [II], or a pharmaceutically acceptable salt thereof, is used in combination with sitagliptin is provided.
In still another embodiment, a medicament for use in treating or preventing type 2 diabetes, comprising sitagliptin, wherein sitagliptin is used in combination with a compound of Formula [II]:
or a pharmaceutically acceptable salt thereof, is provided.
In still another embodiment, a pharmaceutical composition for use in treating or preventing diabetes, obesity, or diabetic complications, comprising a compound of Formula [II]:
or a pharmaceutically acceptable salt thereof, and at least one drug selected from dapagliflozin and sitagliptin is provided.
In still another embodiment, a pharmaceutical composition for use in treating or preventing diabetes, comprising a compound of Formula [II]:
or a pharmaceutically acceptable salt thereof, and at least one drug selected from dapagliflozin and sitagliptin is provided.
In still another embodiment, a pharmaceutical composition for use in treating or preventing type 2 diabetes, comprising a compound of Formula [II]:
or a pharmaceutically acceptable salt thereof, and at least one drug selected from dapagliflozin and sitagliptin is provided.
In still another embodiment, a pharmaceutical composition for use in treating or preventing type 2 diabetes, comprising a compound of Formula [II]:
or a pharmaceutically acceptable salt thereof, and dapagliflozin is provided.
In still another embodiment, a pharmaceutical composition for use in treating or preventing type 2 diabetes, comprising a compound of Formula [II]:
or a pharmaceutically acceptable salt thereof, and sitagliptin is provided.
The drug used herein means any of drugs selected from SGLT1 inhibitors, SGLT2 inhibitors, and DPP4 inhibitors. Administering a drug to a subject who is subject to treatment with another drug is one embodiment of combination use; for example, when a drug is administered to a subject, the combination use includes administration of the drug to the subject while a therapeutically effective amount of an active ingredient included in another drug that has been administered is present in the body of the subject.
A therapeutically effective amount of an SGLT1 inhibitor herein may vary depending on subjects to be administered, administration routes, intended diseases, symptoms, severity of diseases, and combination thereof. When a human (60 kg of body weight) is orally administered, the lower limit of the therapeutically effective amount includes, for example, about 0.01 mg, about 0.1 mg, about 0.5 mg, about 1 mg, about 10 mg, about 20 mg, or about 50 mg per day, and the upper limit of the therapeutically effective amount includes, for example, about 1 mg, about 5 mg, about 10 mg, about 20 mg, about 50 mg, about 100 mg, about 200 mg, about 500 mg, or about 1000 mg per day.
A therapeutically effective amount of an SGLT2 inhibitor (e.g., dapagliflozin) herein may vary depending on subjects to be administered, administration routes, intended diseases, symptoms, severity of diseases, and combination thereof. When a human (60 kg of body weight) is orally administered, the lower limit of the therapeutically effective amount includes, for example, about 0.01 mg, about 0.1 mg, about 0.5 mg, about 1 mg, about 10 mg, about 20 mg, or about 50 mg per day, and the upper limit of the therapeutically effective amount includes, for example, about 1 mg, about 5 mg, about 10 mg, about 20 mg, about 50 mg, about 100 mg, about 200 mg, about 500 mg, or about 1000 mg per day. In one embodiment, the therapeutically effective amount of an SGLT2 inhibitor (e.g., dapagliflozin) is about 1 mg, about 2 mg, about 3 mg, about 4 mg, about 5 mg, about 10 mg, about 12 mg, or about 15 mg per day. In another embodiment, the therapeutically effective amount of an SGLT2 inhibitor (e.g., dapagliflozin) is about 5 mg or about 10 mg per day.
A therapeutically effective amount of a DPP4 inhibitor (e.g., sitagliptin) herein may vary depending on subjects to be administered, administration routes, intended diseases, symptoms, severity of diseases, and combination thereof. When a human (60 kg of body weight) is orally administered, the lower limit of the therapeutically effective amount includes, for example, about 0.01 mg, about 0.1 mg, about 0.5 mg, about 1 mg, about 10 mg, about 20 mg, or about 50 mg per day, and the upper limit of the therapeutically effective amount includes, for example, about 1 mg, about 5 mg, about 10 mg, about 20 mg, about 50 mg, about 100 mg, about 200 mg, about 500 mg, or about 1000 mg per day. In one embodiment, the therapeutically effective amount of a DPP4 inhibitor (e.g., sitagliptin) is about 2.5 mg, about 5 mg, about 10 mg, about 12.5 g, about 25 mg, about 50 mg, about 75 mg, about 100 mg, about 125 mg, about 150 mg, about 175 mg, or about 200 mg per day. In another embodiment, the therapeutically effective amount of a DPP4 inhibitor (e.g., sitagliptin) is about 12.5 mg, about 25 mg, about 50 mg, or about 100 mg per day.
The frequency of administration for drugs, medicaments, and pharmaceutical compositions herein includes once, twice, thrice, or more per day.
The term “treatment” used herein includes the amelioration of conditions, prevention of aggravation, maintenance of remission, prevention of exacerbation, and prevention of relapse.
The term “prevention” used herein includes delaying the onset of conditions. For example, the “prevention of diabetes” includes delaying the onset of type 2 diabetes in impaired glucose tolerance.
A pharmaceutical composition herein may be prepared from a therapeutically effective amount of each drug comprised and at least one or more pharmaceutically acceptable carriers, optionally followed by mixing, according to methods known in the art of medicinal preparations. The amount of each drug comprised in the pharmaceutical composition varies depending on a factor such as dosage forms and dosage amounts and ranges, for example, from 0.1 to 100% by weight of the total amount of the composition.
A dosage form of each drug, medicament, and pharmaceutical composition herein includes oral preparations such as tablets, capsules, granules, powders, lozenges, syrups, emulsions, and suspensions; and parenteral preparations such as external preparations, suppositories, injections, eye drops, nasal preparations, and pulmonary preparations.
The term “pharmaceutically acceptable carrier” includes various organic or inorganic carrier substances which are conventionally used for a component of a formulation. Such substances include, for example, excipients, disintegrants, binders, fluidizers, and lubricants for solid preparations; solvents, solubilization agents, suspending agents, tonicity agents, buffering agents, and soothing agents for liquid preparations; and bases, emulsifying agents, wetting agents, stabilizers, stabilizing agents, dispersing agents, plasticizing agents, pH adjusters, absorption promoters, gelators, antiseptic agents, bulking agents, solubilizers, solubilization agents, and suspending agents for semisolid preparations. Additives such as preserving agents, antioxidant agents, coloring agents, and sweetening agents may be further added, if needed.
Such an “excipient” includes, for example, lactose, white soft sugar, D-mannitol, D-sorbitol, corn starch, dextrin, microcrystalline cellulose, crystalline cellulose, carmellose, carmellose calcium, sodium carboxymethylstarch, low-substituted hydroxypropylcellulose, and gum arabic.
Such a “disintegrant” includes, for example, carmellose, carmellose calcium, carmellose sodium, sodium carboxymethylstarch, croscarmellose sodium, crospovidone, low-substituted hydroxypropylcellulose, hydroxypropylmethyl cellulose, and crystalline cellulose.
Such a “binder” includes, for example, hydroxypropylcellulose, hydroxypropylmethyl cellulose, povidone, crystalline cellulose, white soft sugar, dextrin, starch, gelatin, carmellose sodium, and gum arabic.
Such a “fluidizer” includes, for example, light anhydrous silicic acid and magnesium stearate.
Such a “lubricant” includes, for example, magnesium stearate, calcium stearate, and talc.
Such a “solvent” includes, for example, purified water, ethanol, propylene glycol, macrogol, sesame oil, corn oil, and olive oil.
Such a “solubilization agent” includes, for example, propylene glycol, D-mannitol, benzyl benzoate, ethanol, triethanolamine, sodium carbonate, and sodium citrate.
Such a “suspending agent” includes, for example, benzalkonium chloride, carmellose, hydroxypropylcellulose, propylene glycol, povidone, methylcellulose, and glyceryl monostearate.
Such a “tonicity agent” includes, for example, glucose, D-sorbitol, sodium chloride, and D-mannitol.
Such a “buffering agent” includes, for example, disodium hydrogen phosphate, sodium acetate, sodium carbonate, and sodium citrate.
Such a “soothing agent” includes, for example, benzyl alcohol.
Such a “base” includes, for example, water, oils from animals or vegetables such as olive oil, corn oil, arachis oil, sesame oil, and castor oil, lower alcohols such as ethanol, propanol, propylene glycol, 1,3-butylene glycol, and phenol, higher fatty acids and esters thereof, waxes, higher alcohol, polyhydric alcohol, hydrocarbons such as white petrolatum, liquid paraffin, and paraffin, hydrophilic petrolatum, purified lanolin, absorption ointment, hydrous lanolin, hydrophilic ointment, starch, pullulan, gum arabic, tragacanth gum, gelatin, dextran, cellulose derivatives such as methylcellulose, carboxymethyl cellulose, hydroxyethyl cellulose, and hydroxypropyl cellulose, synthetic polymers such as carboxyvinyl polymer, sodium polyacrylate, polyvinylalcohol, and polyvinylpyrrolidone, propylene glycol, macrogol such as Macrogol 200 to 600, and a combination of two or more of them.
Such a “preserving agent” includes, for example, ethyl parahydroxybenzoate, chlorobutanol, benzyl alcohol, sodium dehydroacetate, and sorbic acid.
Such an “anti-oxidant agent” includes, for example, sodium sulfite and ascorbic acid.
Such a “coloring agent” includes, for example, food colors (e.g., Food Red No. 2 or No. 3, Food Yellow No. 4, or No. 5) and β-carotene.
Such a “sweetening agent” includes, for example, saccharin sodium, dipotassium glycyrrhizinate, and aspartame.
Each drug, medicament, and pharmaceutical composition herein may be administered orally or parenterally (e.g., topically, rectally, intravenously, intramuscularly, and subcutaneously) to humans as well as mammals other than humans such as mice, rats, hamsters, guinea pigs, rabbits, cats, dogs, pigs, cows, horses, sheep, and monkeys. Dosage amounts vary depending on subjects to be administered, diseases, conditions, dosage forms, and administration routes. For example, a daily dose for oral administration to an adult patient (60 kg of body weight) typically ranges from about 0.01 mg to about 1 g of the active ingredient of each drug. The dose can be administered at one time or in divided doses. In one embodiment, each drug may be formulated into several separate pharmaceutical compositions which may be administered to a subject in any order in different administration routes. In another embodiment, a dosage amount of each drug may be reduced in combination use compared to administration of each drug alone, and the daily dose for oral administration to an adult patient (60 kg of body weight) ranges from about 0.01 mg to about 1000 mg.
In one embodiment, a kit such as kits for administration, treatment, and/or prevention, a package such as packaged goods, or a set and/or case of drugs which comprises an SGLT1 inhibitor, e.g., a compound of Formula [I] or a pharmaceutically acceptable salt thereof, at least one drug selected from an SGLT2 inhibitor and a DPP4 inhibitor, and a written matter concerning these drugs indicating that these drugs may or should be used for treatment and/or prevention may be provided. The kit, package, and set of drugs may comprise one or more containers filled with an SGLT1 inhibitor, at least one drug selected from an SGLT2 inhibitor and a DPP4 inhibitor, and optionally, other drugs or medicines (or ingredients). Examples of the kit, package, and set of drugs herein include commercial kits, commercial packages, and commercial medicine set for appropriate use in treatment and/or prevention of intended diseases. The written matter comprised in the kit, package, and set of drugs includes a cautionary note or package insert in the form designated by the government organization that regulates manufacturing, use, or sales of pharmaceutical or biological products which ensures an approval by the government organization on manufacturing, use, or sales of products associated with administration to humans. The kit, package, and set of drugs may include packaged products as well as structures configured for appropriate administration steps and configured so as to be able to achieve more preferable medical treatment and/or prevention including treatment and/or prevention of intended diseases.
General preparation methods of a compound of Formula [I], or a pharmaceutically acceptable salt thereof, are illustrated as follows. A method of preparing a compound of Formula [I], or a pharmaceutically acceptable salt thereof, is not limited thereto.
Each compound obtained in each step may be isolated and/or purified, if necessary, according to any of known methods such as distillation, recrystallization, and column chromatography, or optionally, a subsequent step can proceed without isolation and/or purification.
Herein, the term “room temperature” refers to a temperature which has not been controlled and includes 1° C. to 40° C. as one embodiment.
A compound of Formula [I], or a pharmaceutically acceptable salt thereof, wherein R3 is pyridyl substituted with R3A, or pyrazinyl, pyrimidinyl or pyridazinyl which may be optionally substituted with R3B may be obtained by, for example, the following preparation process.
In the scheme, R1 and R2 have the same meanings as defined above;
R31 is pyridyl substituted with R3A, or pyrazinyl, pyrimidinyl or pyridazinyl which may be optionally substituted with R3B;
R3A and R3B have the same meanings as defined above;
X1A and X1B are each independently halogen, and X1A is more reactive than X1B in step 1;
when R1 is halogen, R1 is preferably the same halogen as X1A;
A4 is n-butyl;
A7 is C1-4 alkyl or benzyl; and
A12 is tert-butyl or benzyl.
Compound [3] may be obtained by reacting Compound [1] with Compound [2] in a solvent in the presence of a base.
The solvent used herein includes, for example, ether solvents such as 1,2-dimethoxyethane; and polar solvents such as N,N-dimethylformamide, N-methylpyrrolidone, 1,3-dimethyl-2-imidazolidinone, and N,N′-dimethylpropyleneurea. The solvent is preferably 1,3-dimethyl-2-imidazolidinone.
The base used herein includes, for example, cesium carbonate and sodium hydride. The base is preferably sodium hydride.
The reaction temperature used herein ranges, for example, from 60° C. to 170° C., preferably from 100° C. to 140° C.
Both Compound [1] and Compound [2] may be commercially available or prepared by known methods.
Alternatively, when R2 is trifluoromethyl, Compound [3] may be commercially available.
Compound [5] may be obtained by reacting Compound [3] with Compound [4] under the Mizoroki-Heck reaction. For example, Compound [5] may be obtained by reacting Compound [3] with Compound [4] in a solvent in the presence of a palladium catalyst and a base.
The solvent used herein includes, for example, alcohol solvents such as ethylene glycol; and polar solvents such as N,N-dimethylformamide. The solvent is preferably ethylene glycol.
The palladium catalyst used herein includes, for example, a mixture of palladium (II) acetate and 1,1′-bis(diphenylphosphino)ferrocene or 1,3-bis(diphenylphosphino)propane. The palladium catalyst is preferably a mixture of palladium (II) acetate and 1,1′-bis(diphenylphosphino)ferrocene.
The base used herein includes, for example, organic bases such as triethylamine. The base is preferably triethylamine.
The reaction temperature used herein ranges, for example, from 80° C. to 150° C., preferably from 100° C. to 140° C.
Compound [4] may be commercially available or prepared by known methods.
Compound [6] may be obtained by converting —C(═CH2)OA4 group of Compound [5] into —C(═O)CH3 group. For example, Compound [6] may be obtained by reacting Compound [5] in a solvent in the presence of an acid.
The solvent used herein includes, for example, ketone solvents such as acetone; alcohol solvents such as ethylene glycol; ether solvents such as tetrahydrofuran and 1,4-dioxane; halogenated hydrocarbon solvents such as dichloromethane; polar solvents such as N,N-dimethylformamide; water; and a mixed solvent of any of these solvents. The solvent is preferably a mixed solvent of tetrahydrofuran and water.
The acid used herein includes, for example, hydrochloric acid and trifluoroacetic acid. The acid is preferably hydrochloric acid.
The reaction temperature herein ranges, for example, from 20° C. to 50° C., and is preferably room temperature.
Compound [8] may be obtained by reacting Compound [6] with Compound [7] in a solvent in the presence of a base.
The solvent used herein includes, for example, ether solvents such as tetrahydrofuran, diethyl ether, and 1,2-dimethoxyethane; alcohol solvents such as methanol and ethanol; hydrocarbon solvents such as toluene; polar solvents such as N,N-dimethylformamide; and a mixed solvent of any of these solvents. The solvent is preferably tetrahydrofuran.
The base used herein includes, for example, lithium tert-butoxide, sodium tert-butoxide, potassium tert-butoxide, sodium methoxide, sodium ethoxide, lithium diisopropylamide, lithium hexamethyldisilazane, and sodium hydride. The base is preferably lithium tert-butoxide.
The reaction temperature herein ranges, for example, from −78° C. to 110° C., preferably from 0° C. to room temperature.
Compound [7] may be commercially available or prepared by known methods.
Compound [10] may be obtained by reacting Compound [8] with Compound [9] in a solvent in the presence of an acid.
The solvent used herein includes, for example, ether solvents such as tetrahydrofuran; alcohol solvents such as methanol and ethanol; hydrocarbon solvents such as toluene.
The acid used herein includes, for example, hydrochloric acid, sulfuric acid, acetic acid, trifluoroacetic acid, and p-toluenesulfonic acid. The acid is preferably acetic acid. These acids may also be used for the solvent.
The reaction temperature herein ranges, for example, from 20° C. to 130° C., preferably from 80° C. to 110° C.
Compound [9] may be commercially available or prepared by known methods, or may also be obtained by General Preparation B as below.
Compound [11] may be obtained by removing -A7 group of Compound [10]. The removal reaction may be carried out under suitable conditions depending on A7. For example, when A7 is ethyl, Compound [11] may be obtained by reacting Compound [10] in a solvent in the presence of a base.
The solvent used herein includes, for example, alcohol solvents such as methanol and ethanol; ether solvents such as tetrahydrofuran; water; and a mixed solvent of any of these solvents. The solvent is preferably a mixed solvent of two or more selected from the group consisting of methanol, tetrahydrofuran, and water.
The base used herein includes, for example, lithium hydroxide, sodium hydroxide, and potassium hydroxide. The base is preferably sodium hydroxide.
The reaction temperature herein ranges, for example, from 0° C. to 100° C., preferably from room temperature to 40° C.
Compound [13] may be obtained by reacting Compound [11] with Compound [12] under the Curtius rearrangement reaction. For example, Compound [13] may be obtained by reacting Compound [11] with an azidating agent in a solvent in the presence of a base, followed by reaction with Compound [12].
The solvent used herein includes, for example, ether solvents such as tetrahydrofuran and 1,4-dioxane; and hydrocarbon solvents such as toluene. Alternatively, Compound [12] may also be used for the solvent. The solvent is preferably toluene or a mixed solvent of toluene and Compound [12].
The azidating agent used herein includes, for example, diphenylphosphoryl azide.
The base used herein includes, for example, organic bases such as triethylamine and N,N-diisopropylethylamine. The base is preferably triethylamine.
The reaction temperature herein ranges, for example, from 65° C. to 130° C., preferably from 90° C. to 110° C.
Compound [12] may be commercially available or prepared by known methods.
Compound [14] may be obtaind by removing —C(═O)OA12 group of Compound [13] in a solvent. The removal reaction may be carried out under suitable conditions depending on A12. For example, when A12 is tert-butyl, Compound [14] may be obtained by reacting Compound [13] in a solvent in the presence of an acid.
The solvent used herein includes, for example, ester solvents such as ethyl acetate; alcohol solvents such as methanol and ethanol; ether solvents such as tetrahydrofuran and 1,4-dioxane; halogenated hydrocarbon solvents such as dichloromethane; water; and a mixed solvent of any of these solvents. The solvent is preferably 1,4-dioxane.
The acid used herein includes, for example, hydrochloric acid, sulfuric acid, and trifluoroacetic acid. The acid is preferably hydrochloric acid. These acids may also be used for the solvent.
The reaction temperature herein ranges, for example, from 0° C. to 60° C., preferably from 0° C. to room temperature.
Compound [I-1] may be obtained by condensation reaction of Compound [14] and Compound [15] in a solvent.
The solvent used herein includes, for example, halogenated hydrocarbon solvents such as chloroform; ether solvents such as tetrahydrofuran; polar solvents such as pyridine, acetonitrile, and N,N-dimethylformamide; and a mixed solvent of any of these solvents. The solvent is preferably pyridine.
The condensation agent used herein includes, for example, dicyclohexylcarbodiimide (DCC), 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (WSCHC1), diisopropylcarbodiimide, 1,1′-carbonyldiimidazole (CDI), 0-(7-azabenzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium hexafluorophosphate (HATU), {{[(1-cyano-2-ethoxy-2-oxoethylidene)amino]oxy}-4-morpholinomethylene}dimethylammonium hexafluorophosphate (COMU), 4-(4,6-dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride n-hydrate (DMT-MM), (benzotriazol-1-yloxy)tripyrrolidinophosphonium hexafluorophosphate (PyBOP), diphenylphosphoryl azide, and propylphosphonic acid anhydride. The condensation agent is preferably 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (WSC.HCl).
The reaction temperature herein ranges, for example, from 0° C. to 100° C., and is preferably room temperature.
Compound [15] may be obtained by, for example, General Preparation E as mentioned below.
Compound [9] may be obtained by, for example, the following preparation method.
In the scheme, R31 has the same meaning as defined above, and X16 is halogen.
Compound [9] may be obtained by reacting Compound [16] with hydrazine monohydrate in a solvent.
The solvent used herein includes, for example, ether solvents such as tetrahydrofuran and 1,4-dioxane; alcohol solvents such as ethanol and 2-propanol; halogenated hydrocarbon solvents such as dichloromethane; polar solvents such as N,N-dimethylformamide and pyridine; water; and a mixed solvent of any of these solvents. Alternatively, hydrazine monohydrate may also be used for the solvent. The solvent is preferably a mixed solvent of 2-propanol and hydrazine monohydrate.
The reaction temperature herein ranges, for example, from room temperature to 140° C., preferably from 60° C. to 100° C.
Compound [16] may be commercially available or prepared by known methods.
When R31 is pyridyl substituted with R3A, Compound [9] may also be obtained by, for example, the following preparation method.
In the scheme, R31 is pyridyl substituted with R3A, and R3A has the same meaning as defined above.
Compound [9] may be obtained by diazotizing Compound [17] in a solvent in the presence of an acid, followed by reduction.
The solvent used herein includes, for example, water.
The diazotization agent used herein includes, for example, sodium nitrite.
The acid used herein includes, for example, hydrochloric acid and sulfuric acid. The acid is preferably hydrochloric acid.
The reducing agent used herein includes, for example, tin (II) chloride and sodium sulfite. The reducing agent is preferably tin (II) chloride.
The reaction temperature of the diazotization ranges, for example, from −20° C. to 5° C., preferably from −5° C. to 0° C.
The reaction temperature of the reduction ranges, for example, from −5° C. to room temperature, preferably from 0° C. to room temperature.
Compound [17] may be commercially available or prepared by known methods.
Alternatively, when R31 is (1) pyridyl substituted with R3A or (2) pyrimidinyl optionally substituted with R3B, Compound [9] may also be obtained by, for example, the following preparation method.
In the scheme, R31 is (1) pyridyl substituted with R3A or (2) pyrimidinyl optionally substituted with R3B,
R3A, R3B, and X16 have the same meanings as defined above, and
A19 is tert-butoxycarbonyl or benzyloxycarbonyl.
Compound [18] may be obtained by reacting Compound [16] with a base and borate ester in a solvent.
The solvent used herein includes, for example, ether solvents such as tetrahydrofuran; hydrocarbon solvents such as toluene; and a mixed solvent of any of these solvents. The solvent is preferably tetrahydrofuran.
The base used herein includes, for example, n-butyllithium and isopropylmagnesium bromide. The base is preferably n-butyllithium.
The borate ester used herein includes, for example, triisopropyl borate and trimethyl borate. The borate ester is preferably triisopropyl borate.
The reaction temperature herein ranges, for example, from −78° C. to room temperature, preferably from −78° C. to 0° C.
Compound [16] may be commercially available or prepared by known methods.
Compound [20] may be obtained by reacting Compound [18] with Compound [19] in a solvent in the presence of a copper catalyst.
The solvent used herein includes, for example, ether solvents such as tetrahydrofuran; and alcohol solvents such as methanol. The solvent is preferably methanol.
The copper catalyst used herein includes, for example, copper (II) acetate.
The reaction temperature herein ranges, for example, from room temperature to 100° C., preferably from 45° C. to 65° C.
Compound [9] may be obtained by removing -A19 group of Compound [20] in a solvent. The removal reaction may be carried out under suitable conditions depending on A19. For example, when A19 is tert-butoxycarbonyl, Compound [9] may be obtained by reacting Compound [20] in a solvent in the presence of an acid.
The solvent used herein includes, for example, ester solvents such as ethyl acetate; alcohol solvents such as methanol and ethanol; ether solvents such as tetrahydrofuran and 1,4-dioxane; halogenated hydrocarbon solvents such as dichloromethane; water; and a mixed solvent of any of these solvents. The solvent is preferably 1,4-dioxane.
The acid used herein includes, for example, hydrochloric acid, sulfuric acid, and trifluoroacetic acid. The acid is preferably hydrochloric acid.
The reaction temperature herein ranges, for example, from 0° C. to 60° C., preferably from 0° C. to room temperature.
A compound of Formula [I] wherein R3 is C1-6 alkyl or halo-C1-6 alkyl, or a pharmaceutically acceptable salt thereof, may be obtained by, for example, any of the following preparation methods.
In the scheme, R1 and R2 have the same meanings as defined above, and R32 is C1-6 alkyl or halo-C1-6 alkyl.
A compound of Formula [I-2] may be prepared by reacting Compound [21] or a salt thereof with Compound [15] or a salt thereof in the presence of a condensation agent and additive in a solvent.
The condensation agent used herein includes, for example, dicyclohexylcarbodiimide (DCC), 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (WSC.HCl), diisopropylcarbodiimide, 1,1′-carbonyldiimidazole (CDI), 0-(7-azabenzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium hexafluorophosphate (HATU), {{[(1-cyano-2-ethoxy-2-oxoethylidene)amino]oxy}-4-morpholinomethylene}dimethylammonium hexafluorophosphate (COMU), 4-(4,6-dimethoxy-1,3,5-triazin-2-yl) methylmorpholinium chloride n-hydrate (DMT-MM), (benzotriazol-1-yloxy)tripyrrolidinophosphonium hexafluorophosphate (PyBOP), diphenylphosphoryl azide, and propylphosphonic acid anhydride.
The additive used herein includes, for example, 1-hydroxybenzotriazole (HOBt), 1-hydroxy-7-azabenzotriazole (HOAt), N-hydroxysuccinimide (HOSu), 4-dimethylaminopyridine, and 1-methylimidazole.
The solvent used herein includes, for example, halogenated hydrocarbon solvents such as chloroform; ether solvents such as tetrahydrofuran; polar solvents such as pyridine, acetonitrile, and N,N-dimethylformamide; and a mixed solvent of any of these solvents.
The reaction temperature herein ranges, for example, from 0° C. to 100° C.
When a salt of Compound [21] is used, then the reaction may be carried out in the presence of a base. Such a base includes, for example, organic bases such as triethylamine, and alkali metal salts such as sodium carbonate.
A compound of Formula [1-2] may also be prepared by converting Compound [15] with a halogenating agent into carboxylic acid halide in a solvent, followed by reaction with Compound [21] in the presence of a base.
The halogenating agent used in the reaction includes, for example, oxalyl chloride and thionyl chloride. A preferable halogenating agent is oxalyl chloride.
The base used in the reaction includes, for example, organic bases such as pyridine, triethylamine, and N,N-diisopropylethylamine; and alkali metal salts such as sodium hydrogen carbonate and sodium carbonate. A preferable base is pyridine.
The solvent used herein includes, for example, halogenated hydrocarbon solvents such as chloroform; ether solvents such as cyclopentylmethyl ether, and tetrahydrofuran; hydrocarbon solvents such as toluene; and a mixed solvent of any of these solvents and water. A preferable solvent is chloroform.
The reaction temperature herein ranges, for example, from 0° C. to 80° C., preferably from 0° C. to 60° C.
In the preparation of carboxylic acid halide, N,N-dimethylformamide may be added as an additive.
In the scheme, R1, R2, and R32 have the same meanings as defined above, and PN1 is a protective group of the amino group. A preferable PN1 is 2,4-dimethoxybenzyl group.
Compound [23] may be prepared from Compound [21] or a salt thereof and Compound [22] or a salt thereof according to Preparation C1 Step C1-1.
A compound of Formula [I-2] or a salt thereof may be prepared by removing PN1 from Compound [23] via a deprotection reaction. The deprotection reaction may be carried out under suitable conditions depending on PN1.
For example, when PN1 is 2,4-dimethoxybenzyl group, a compound of Formula [I-2] or a salt thereof may be prepared by reaction with an acid in the presence of an additive in a solvent.
The acid used herein includes, for example, methanesulfonic acid, p-toluenesulfonic acid, and trifluoroacetic acid. A preferable acid is trifluoroacetic acid.
The additive used herein includes, for example, anisole and triethylsilane. A preferable additive is anisole.
The solvent used herein includes, for example, halogenated hydrocarbon solvents such as dichloromethane, hydrocarbon solvents such as toluene, water, and a mixed solvent of any of these solvents. An organic acid such as trifluoroacetic acid may also be used for the solvent.
The reaction temperature herein ranges, for example, from 0° C. to 130° C., preferably from 25° C. to 80° C.
When an acid is used in this step, Compound [24]:
wherein R1 and R32 have the same meanings as defined above, or a salt thereof, is obtained. A compound of Formula [I-2] or a salt thereof may be prepared by converting hydroxyl group into C1-6 alkyl-O or halo-C1-6 alkyl-O group in Compound [24] or a salt thereof according to any of known methods.
For example, a compound of Formula [I-2] wherein R1 is fluorine, R2 is tert-butyl, and R32 is trifluoromethyl (i.e., a compound of Formula [II]) or a salt thereof may be prepared by reacting Compound [24] or a salt thereof with di-tert-butyl dicarbonate in the presence of magnesium perchlorate.
The solvent used herein includes, for example, halogenated hydrocarbon solvents such as chloroform, and ether solvents such as tetrahydrofuran. A preferable solvent is chloroform.
The reaction temperature herein ranges, for example, from 0° C. to 100° C., preferably from room temperature to 70° C.
Compound [21] may be prepared by the following preparation methods.
In the scheme, R1, R2, and R32 have the same meanings as defined above, and L1 is a leaving group. L1 is preferably chlorine, bromine, or iodine.
PN2 is each independently a protective group of amine. The two PN2 is are preferably combined with the nitrogen atom to which they are attached to form 2,5-dimethylpyrrole.
Compound [26] may be prepared by introducing PN2 into the amino group in Compound [25] or a salt thereof according to any of known methods. The introduction of the protective group may be carried out under suitable conditions depending on PN2. For example, when the two PN2s are combined with the nitrogen atom to which they are attached to form 2,5-dimethylpyrrole, Compound [26] may be prepared by reacting Compound [25] with 2,5-hexanedione in a solvent under the acidic condition.
The acid used herein includes, for example, concentrated hydrochloric acid, concentrated sulfuric acid, amidosulfuric acid, p-toluenesulfonic acid, and acetic acid. A preferable acid is acetic acid.
The solvent used herein includes, for example, alcohol solvents such as ethanol, ether solvents such as tetrahydrofuran, hydrocarbon solvents such as toluene, polar solvents such as N,N-dimethylformamide, halogenated hydrocarbon solvents such as dichloroethane, and a mixed solvent of any of these solvents. An organic acid such as acetic acid may also be used for the solvent.
The reaction temperature herein ranges, for example, from room temperature to 150° C., preferably from 80° C. to 140° C.
Compound [27] may be prepared by alkylating or haloalkylating Compound [26] according to any of known methods. For example, when R32 is trifluoromethyl, the compound may be prepared by a process comprising:
Step (a): reacting Compound [26] with dibromodifluoromethane in the presence of a base and a catalyst in a solvent, and
Step (b): fluorinating the resultant in the presence of tetramethylammonium fluoride or silver (I) tetrafluoroborate in a solvent.
The base used in the Step (a) includes, for example, sodium hydride and potassium tert-butoxide. A preferable base is sodium hydride.
The catalyst used in the Step (a) includes, for example, tetrabutylammonium bromide and zinc. A preferable catalyst is tetrabutylammonium bromide.
The solvent used in the Step (a) includes, for example, ether solvents such as tetrahydrofuran, and polar solvents such as N,N-dimethylformamide. A preferable solvent is N,N-dimethylformamide.
The reaction temperature in the Step (a) ranges, for example, from 0° C. to 40° C., preferably from 0° C. to room temperature.
When tetramethylammonium fluoride is used in Step (b), the solvent used therein includes, for example, ether solvents such as 1,4-dioxane, and polar solvents such as sulfolane. A preferable solvent is sulfolane. When silver (I) tetrafluoroborate is used in Step (b), the solvent used therein includes, for example, halogenated hydrocarbon solvents such as dichloromethane. A preferable solvent is dichloromethane.
When tetramethylammonium fluoride is used in Step (b), the reaction temperature therein ranges, for example, from 80° C. to 180° C., preferably from 100° C. to 140° C. When silver (I) tetrafluoroborate is used in Step (b), the reaction temperature therein ranges, for example, from −78° C. to 50° C., preferably from −78° C. to room temperature.
Compound [28] may be prepared by introducing L1 into Compound [27] in the presence of a base in a solvent. For example, when L1 is iodine, Compound [28] may be prepared by iodizing Compound [27] in the presence of a base in a solvent.
The base used herein includes, for example, n-butyllithium, lithium diisopropylamide, lithium hexamethyldisilazide, and lithium tetramethylpiperidide. A preferable base is n-butyllithium.
The iodizing agent used herein includes, for example, iodine, iodine monochloride, N-iodosuccinimide, and 1-chloro-2-iodoethane. A preferable iodizing agent is iodine.
The solvent used herein includes, for example, ether solvents such as tetrahydrofuran, hydrocarbon solvents such as toluene, and a mixed solvent of any of these solvents. A preferable solvent is tetrahydrofuran.
The reaction temperature herein ranges, for example, from −100° C. to 40° C., preferably from −78° C. to 20° C.
Compound [29] or a salt thereof may be prepared by removing PN2 from Compound [28] via a deprotection reaction. The deprotection reaction may be carried out under suitable conditions depending on PN2. For example, when the two PN2s are combined with the nitrogen atom to which they are attached to form 2,5-dimethylpyrrole, Compound [29] or a salt thereof may be prepared by reacting Compound [28] with hydroxylamine in a solvent.
The solvent used herein includes, for example, alcohol solvents such as ethanol, water, and a mixed solvent of any of these solvents. A preferable solvent is a mixed solvent of an alcohol solvent with water.
The reaction temperature herein ranges, for example, from 40° C. to 150° C., preferably from 80° C. to 130° C.
Hydroxylamine hydrochloride may be used instead of hydroxylamine. In that case, the reaction may be carried out in the presence of a base. The base used herein includes, for example, organic bases such as triethylamine, and alkali metal salts such as sodium carbonate. A preferable base is triethylamine.
Compound [21] or a salt thereof may be prepared via Suzuki coupling reaction of Compound [29] or a salt thereof with Compound [30]. For example, Compound [21] or a salt thereof may be prepared by reacting Compound [29] or a salt thereof with Compound [30] in the presence of a base and palladium catalyst in a solvent.
The palladium catalyst used in the reaction includes, for example, tetrakis(triphenylphosphine)palladium, [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium (II)-dichloromethane adduct, [1,1′-bis(di-tert-butylphosphino)ferrocene]dichloropalladium (II), and a mixture of palladium (II) acetate and tricyclohexylphosphine, 2-dicyclohexylphosphino-2′,6′-dimethoxybiphenyl, or 2-dicyclohexylphosphino-2′,4′,6′-triisopropylbiphenyl. A preferable palladium catalyst is [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium (II)-dichloromethane adduct.
The base used in the reaction includes, for example, tripotassium phosphate, cesium carbonate, sodium carbonate, sodium hydrogen carbonate, potassium carbonate, and triethylamine. A preferable base is tripotassium phosphate, cesium carbonate, or sodium carbonate.
The solvent used herein includes, for example, ether solvents such as 1,4-dioxane, tetrahydrofuran, diethyl ether, and 1,2-dimethoxyethane; alcohol solvents such as methanol, ethanol, 1-propanol, and 2-propanol; hydrocarbon solvents such as toluene, n-hexane, and xylene; polar solvents such as N,N-dimethylformamide, dimethyl sulfoxide, and acetonitrile; and a mixed solvent of any of these solvents with water. A preferable solvent is 1,2-dimethoxyethane, toluene, dimethyl sulfoxide, or a mixed solvent of any of these solvents with water.
The reaction temperature herein ranges, for example, from 20° C. to 150° C., preferably from 80° C. to 130° C.
Compound [30] may be prepared according to any of known methods. A corresponding boronic acid ester may be used instead of Compound [30] in the reaction of the step D1-5. For example, such a boronic acid ester [33] may be prepared by the following preparation method.
In the scheme, R1 and R2 have the same meanings as defined above,
R6 is fluorine or hydroxyl group.
L2 is a leaving group. L2 is preferably chlorine, bromine, iodine, p-toluenesulfonyloxy, methanesulfonyloxy, or trifluoromethanesulfonyloxy.
B(OR7)2 is a boronic acid ester. R7 is, for example, each independently methyl, ethyl, propyl, isopropyl, n-butyl, sec-butyl, or tert-butyl, or alternatively, OR7 may combine together with the boron atom to which they attach to form a cyclic boronic acid ester. B(OR7)2 is preferably boronic acid pinacol ester.
Compound [32] may be prepared by converting R1 into tert-butoxy group in Compound [31]. The reaction may be carried out according to any of known methods.
When R1 is fluorine, Compound [32] may be prepared by, for example, reacting Compound [31] with sodium tert-butoxide or potassium tert-butoxide in a solvent. The solvent used herein includes, for example, ether solvents such as tetrahydrofuran; and polar solvents such as N,N-dimethylformamide and dimethyl sulfoxide. A preferable solvent is N,N-dimethylformamide. The reaction temperature herein ranges, for example, from 0° C. to 100° C., preferably from room temperature to 85° C.
When R1 is hydroxyl group, Compound [32] may be prepared according to, for example, Preparation C2 Step C2-2.
Compound [33] may be prepared by reacting Compound [32] with a boron compound in the presence of a palladium catalyst, organic phosphorus compound, and base in a solvent.
The palladium catalyst herein includes, for example, palladium (II) acetate, palladium (II) chloride, and tris(dibenzylideneacetone)dipalladium (0).
The organic phosphorus compound herein includes, for example, triphenylphosphine, tricyclohexylphosphine, 1,1′-bis(diphenylphosphino)ferrocene, 2-dicyclohexylphosphino-2′,6′-dimethoxybiphenyl, 2-dicyclohexylphosphino-2′,4′,6′-triisopropylbiphenyl, and 2-dicyclohexylphosphino-2′-(N,N-dimethylamino)biphenyl.
Instead of the palladium catalyst and the organic phosphorus compound, tetrakis(triphenylphosphine)palladium, [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium (II)-dichloromethane adduct, or [1,1′-bis(di-tert-butylphosphino)ferrocene]dichloropalladium (II) may be used.
The base herein includes, for example, potassium acetate, sodium carbonate, cesium carbonate, and potassium carbonate. A preferable base is potassium acetate.
The boron compound herein includes, for example, bis(pinacolato)diboron.
The solvent herein includes, for example, ether solvents such as 1,4-dioxane, tetrahydrofuran, and 1,2-dimethoxyethane; hydrocarbon solvents such as toluene; and polar solvents such as N,N-dimethylformamide and dimethyl sulfoxide. A preferable solvent is dimethyl sulfoxide.
The reaction temperature herein ranges, for example, from room temperature to 150° C., preferably from 70° C. to 110° C.
Compound [15] or a salt thereof and Compound [22] or a salt thereof may be prepared by the following preparation methods.
In the scheme, PN1 has the same meaning as defined above,
PE1 and PE2 are each independently a protective group for carboxy. Preferably, PE1 and PE2 are each independently methyl, ethyl, tert-butyl, or benzyl.
R8 is each independently methoxy or ethoxy.
L3 is a leaving group. L3 is preferably bromine or chlorine.
Compound [36] may be prepared by reacting Compound [34] with Compound [35] in the presence of a base in a solvent.
The base used in the reaction includes, for example, potassium tert-butoxide, sodium methoxide, sodium ethoxide, lithium diisopropylamide, potassium hexamethyldisilazane, potassium carbonate, cesium carbonate, and sodium hydride. A preferable base is potassium tert-butoxide.
The solvent herein includes, for example, ether solvents such as tetrahydrofuran; alcohol solvents such as methanol and ethanol; and polar solvents such as N,N-dimethylformamide and dimethyl sulfoxide. A preferable solvent is tetrahydrofuran.
The reaction temperature herein ranges, for example, from −78° C. to 100° C., preferably from 0° C. to 70° C.
Compound [37] may be prepared by reacting Compound [36] with formaldehyde (preferably, aqueous formaldehyde solution) in the presence of a base in a solvent.
The base used in the reaction includes, for example, potassium tert-butoxide, sodium methoxide, sodium ethoxide, lithium diisopropylamide, potassium hexamethyldisilazane, potassium carbonate, cesium carbonate, and sodium hydride. A preferable base is potassium carbonate.
The solvent herein includes, for example, ether solvents such as tetrahydrofuran; alcohol solvents such as methanol and ethanol; and polar solvents such as N,N-dimethylformamide and dimethyl sulfoxide. A preferable solvent is tetrahydrofuran.
The reaction temperature herein ranges, for example, from −78° C. to 100° C., preferably from 0° C. to 70° C.
Compound [39] may be prepared by reacting Compound [37] with Compound [38] in a solvent.
The solvent herein includes, for example, hydrocarbon solvents such as toluene; alcohol solvents such as methanol and ethanol; and a mixed solvent of any of these solvents. A preferable solvent is toluene.
The reaction temperature herein ranges, for example, from 20° C. to 150° C., preferably from 80° C. to 130° C.
Compound [40] or a salt thereof may be prepared by removing PE1 from Compound [39] via a deprotection reaction. The deprotection reaction may be carried out under suitable conditions depending on PE1. For example, when PE1 is ethyl, Compound [40] or a salt thereof may be prepared by hydrolyzing Compound [39] in the presence of a base in a solvent.
The base used in the reaction includes, for example, lithium hydroxide, sodium hydroxide, potassium hydroxide, and sodium ethoxide. A preferable base is sodium ethoxide.
The solvent herein includes, for example, alcohol solvents such as ethanol, ether solvents such as tetrahydrofuran, water, and a mixed solvent of any of these solvents. A preferable solvent is a mixed solvent of ethanol and water.
The reaction temperature herein ranges, for example, from 0° C. to 100° C., preferably from 0° C. to 40° C.
Compound [22] or a salt thereof may be obtained by separation from Compound [40] or a salt thereof. The separation of Compound [22] or a salt thereof may be carried out under conditions suitable for the separation according to any of methods well known in the art. For example, Compound [22] or a salt thereof may be obtained by separation of a diastereomer salt thereof with a basic optically resolving reagent, followed by treatment of the salt with an acid.
The basic optically resolving reagent herein includes, for example, (1R,2R)-(−)-2-amino-1-(4-nitrophenyl)-1,3-propanediol.
The solvent used in the conversion into the diastereomer salt includes, for example, alcohol solvents such as 2-propanol, ether solvents such as 1,2-dimethoxyethane, polar solvents such as acetonitrile, and a mixed solvent of any of these solvents with water. A preferable solvent is acetonitrile, 1,2-dimethoxyethane, or a mixed solvent of any of these solvents with water.
The optical purity of the diastereomer salt may be increased by recrystallization. The solvent used in the recrystallization includes, for example, ether solvents such as 1,2-dimethoxyethane, polar solvents such as acetonitrile, and a mixed solvent of any of these solvents with water. A preferable solvent is a mixed solvent of acetonitrile and water.
The acid used in the decomposition of the diastereomer salt includes, for example, hydrochloric acid, sulfuric acid, and potassium hydrogensulfate. A preferable acid is hydrochloric acid.
The solvent used in the decomposition of the diastereomer salt includes, for example, ester solvents such as ethyl acetate, ether solvents such as tetrahydrofuran, water, and a mixed solvent of any of these solvents. A preferable solvent is a mixed solvent of ethyl acetate and water.
Compound [15] or a salt thereof may be prepared by removing PN1 from Compound [22] or a salt thereof via a deprotection reaction. The deprotection reaction may be carried out under suitable conditions depending on PN1. For example, when PN1 is 2,4-dimethoxybenzyl, Compound [15] or a salt thereof may be prepared according to Preparation C2 Step C2-2.
The meanings of abbreviations used herein are shown as follows.
DMSO: dimethyl sulfoxide
THF: tetrahydrofuran
CPME: cyclopentylmethyl ether
WSC.HCl: 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride
Preparations, Examples, Reference Examples, Test Examples, and Formulation Examples are illustrated as below.
1H-NMR spectra were measured in CDCl3 or DMSO-d6 with tetramethylsilane for an internal standard substance, and all δ values are shown in ppm. The measurement was carried out with an NMR spectrometer with 400 MHz, unless otherwise specified.
Symbols in 1H-NMR spectra mean as follows.
s: singlet
d: doublet
t: triplet
q: quartet
dd: double doublet
ddd: double double doublet
brs: broad singlet
m: multiplet
J: coupling constant
To 3-bromo-5-fluorophenol (500 mg) were sequentially added di-tert-butyl dicarbonate (1.14 g) and magnesium perchlorate (58 mg) at room temperature under argon flow. The reaction mixture was stirred at 50° C. for 1 hour 20 minutes. To the reaction mixture was added di-tert-butyl dicarbonate at 50° C. The reaction mixture was stirred at 50° C. for 1 hour and further stirred at 65° C. for 1 hour, and then cooled to room temperature. To the reaction mixture was added di-tert-butyl dicarbonate at room temperature. The reaction mixture was stirred at 65° C. for 3 hours. The reaction mixture was cooled to room temperature, and thereto was added a mixed solution of n-hexane/ethyl acetate (1/1). The reaction mixture was sequentially washed with 3N hydrochloric acid, saturated aqueous sodium hydrogen carbonate solution, and brine, and then dried over sodium sulfate and concentrated. The residue was purified by silica gel column chromatography (eluent: n-hexane/ethyl acetate=1/0 to 20/1) to give the title compound (437 mg) in the yield of 68%.
1H-NMR (CDCl3) δ: 1.35 (s, 9H), 6.62-6.66 (m, 1H), 6.92-6.98 (m, 2H).
To a solution of 1-bromo-3-(tert-butoxy)-5-fluorobenzene (437 mg) obtained in Step 1 in DMSO (5 mL) were sequentially added potassium acetate (434 mg), bis(pinacolato)diboron (898 mg), and [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium (II)-dichloromethane adduct (144 mg) under argon atmosphere at room temperature. The reaction mixture was stirred at 90° C. for 2.5 hours. The reaction mixture was cooled to room temperature. To the reaction mixture were sequentially added a mixed solution of n-hexane/ethyl acetate (1/1) and water. The reaction mixture was stirred at room temperature for 50 minutes and let stand overnight. To the reaction mixture were sequentially added a mixed solution of n-hexane/ethyl acetate (1/1), water, silica gel, and celite. The reaction mixture was stirred, and then insoluble substances were filtered off and the insoluble substances were washed with a mixed solution of n-hexane/ethyl acetate (1/1). The filtrate was extracted with a mixed solution of n-hexane/ethyl acetate (1/1). The organic layer was sequentially washed with water twice and brine, dried over sodium sulfate, and concentrated. The residue was purified by silica gel thin-layer chromatography (eluent: n-hexane/ethyl acetate=10/1) to give the title compound (443 mg) in the yield of 85%.
1H-NMR (CDCl3) δ: 1.33 (s, 12H), 1.36 (s, 9H), 6.77-6.82 (m, 1H), 7.18-7.23 (m, 2H).
To potassium tert-butoxide (180 g) was added THF (2.55 L) at room temperature under nitrogen flow. To the mixture was added dropwise triethyl phosphonoacetate (314 g) under ice cooling over 13 minutes. The dropping funnel used was washed with THF (511 mL), and the washings were added to the reaction mixture. The reaction mixture was stirred for 2 hours 9 minutes under ice cooling. To the reaction mixture was added dropwise ethyl 2-bromopropionate (247 g) over 20 minutes under ice cooling. The dropping funnel used was washed with THF (79 mL), and the washings were added to the reaction mixture. The reaction mixture was stirred at room temperature for 22 hours 45 minutes. To the reaction mixture was added potassium carbonate (188 g) over 1 minute under ice cooling. To the reaction mixture was added dropwise 37% by weight of aqueous formaldehyde solution (152 mL) over 10 minutes under ice cooling. The reaction mixture was stirred at room temperature for 19 hours 44 minutes. To the reaction mixture was added water (1.57 L) at room temperature over 1 minute. The reaction mixture was stirred at room temperature for 1 hour 48 minutes. The reaction mixture was separated. The resulted aqueous layer was extracted with THF (200 mL) twice. The resulted organic layers were combined and concentrated. To the residue were added toluene (471 mL) and brine (471 mL). The reaction mixture was stirred and separated. The organic layer was dried over sodium sulfate (63 g). Sodium sulfate was filtered off. Separately, a similar reaction was performed with triethyl phosphonoacetate (300 g) to give a filtrate, which was then combined with the filtrate obtained above to give a solution of the title compound (equivalent to 2.66 mol) in toluene (about 921 mL). The resulted solution of the title compound in toluene was deemed to afford the yield of 100% and used in the next step. The generation of the title compound was confirmed by HPLC analysis.
The measuring instrument and conditions for HPLC are shown as follows.
Measuring instrument: HPLC system, Shimadzu Corporation, High-Performance Liquid Chromatograph Prominence
Measuring conditions:
Column: Kinetex C18: 2.6 μm, 50 mm×2.1 mm (Phenomenex)
Column temperature: 40° C.
Flow rate: 0.4 mL/min.
Time for analysis: 10 min.
Detection wavelength: UV (220 nm)
Mobile phase: (Solution A) water, (Solution B) acetonitrile
Delivery of mobile phase: A mixing ratio (Solution A/Solution B (volume %)) of Solution A and Solution B was maintained 80/20 from 0 minute to 0.01 minute after injection, changed linearly from 80/20 to 10/90 from 0.01 minute to 7 minutes, maintained 10/90 from 7 minutes to 8 minutes, changed linearly from 10/90 to 80/20 from 8 minutes to 9 minutes, and maintained 80/20 from 9 minutes to 10 minutes.
The retention time of the title compound was about 3.7 minutes under the measuring conditions for HPLC.
To a solution of diethyl 2-methyl-3-methylenesuccinate (equivalent to 2.66 mol) obtained in Step 1 in toluene (about 921 mL) was added dropwise 2,4-dimethoxybenzylamine (468 g) over 2 minutes at room temperature under nitrogen flow. The reaction mixture was stirred at 120° C. for 5 hours 45 minutes. The reaction mixture was let stand for a weekend at room temperature. The reaction mixture was cooled with ice to about 15° C. of the internal temperature. To the reaction mixture was added dropwise 2N hydrochloric acid (1.33 L), and the mixture was stirred. The reaction mixture was separated. The resulted aqueous layer was extracted with toluene (150 mL). The resulted organic layers were combined, washed with a mixed solution of brine and water (600 mL, brine/water=1/1), dried over sodium sulfate (120 g), concentrated, and dried under reduced pressure at room temperature overnight to give a crude product of the title compound (790 g; cis/trans=about 1/1, 5.5% by weight of toluene inclusive). The generation of the title compound was confirmed by HPLC analysis.
The measuring instrument and conditions for HPLC are shown as follows.
Measuring instrument: HPLC system, Shimadzu Corporation, High-Performance Liquid Chromatograph Prominence
Measuring conditions:
Column: Atlantis T3: 5 μm, 150 mm×4.6 mm (Waters)
Column temperature: 40° C.
Flow rate: 1.15 mL/min.
Time for analysis: 18 min.
Detection wavelength: UV (220 nm)
Mobile phase: (Solution A) 10 mM (sodium) phosphate buffer (pH=2.6), (Solution B) acetonitrile
Delivery of Mobile phase: A mixing ratio (Solution A/Solution B (volume %)) of Solution A and Solution B was maintained 60/40 from 0 minute to 0.5 minute after injection, changed linearly from 60/40 to 10/90 from 0.5 minute to 8 minutes, maintained 10/90 from 8 minutes to 12.5 minutes, changed linearly from 10/90 to 60/40 from 12.5 minutes to 13.5 minutes, and maintained 60/40 from 13.5 minutes to 18 minutes.
The retention time was about 6.6 minutes for ethyl (cis)-1-(2,4-dimethoxybenzyl)-4-methyl-5-oxopyrrolidine carboxylate and about 6.9 minutes for ethyl (trans)-1-(2,4-dimethoxybenzyl)-4-methyl-5-oxopyrrolidine-3-carboxylate under the measuring conditions for HPLC.
To a crude mixture (790 g, 5.5% by weight of toluene inclusive) of ethyl (cis)-1-(2,4-dimethoxybenzyl)-4-methyl-5-oxopyrrolidine-3-carboxylate and ethyl (trans)-1-(2,4-dimethoxybenzyl)-4-methyl-5-oxopyrrolidine-3-carboxylate, obtained in step 2, was added ethanol (1.15 L) at room temperature under nitrogen flow. To the reaction mixture was added dropwise sodium ethoxide (20% by weight solution in ethanol, 1.15 L) at room temperature over 31 minutes. The reaction mixture was stirred at room temperature for 2 hours 57 minutes. The reaction mixture was cooled with ice, and thereto was added dropwise water (1.84 L) over 33 minutes. To the reaction mixture were added CPME (1.8 L) and toluene (1.8 L) at room temperature, and the mixture was separated (Organic layer 1). To the resulted aqueous layer was added CPME (1.8 L), and the mixture was separated (Organic layer 2). Solvent (1.8 L) was removed from the resulted aqueous layer by evaporation. To the resulted aqueous layer was added dropwise 6N hydrochloric acid (110 mL) under ice cooling, and thereto was added ethyl acetate (1.8 L). To the mixture was added dropwise 6N hydrochloric acid (300 mL) under ice cooling, and the mixture was stirred for about 10 minutes. To the mixture were sequentially added water (2.2 L), 6N hydrochloric acid (50 mL), water (1.0 L), 10% by weight of aqueous sodium hydrogen sulfate solution (300 mL), and ethanol (300 mL) under ice cooling. The mixture was stirred at room temperature overnight. To the mixture was added ethyl acetate (600 mL), and the mixture was separated. The resulted aqueous layer was extracted with ethyl acetate (600 mL) twice. The resulted organic layers were combined (except for Organic layer 1 and Organic layer 2) and washed with a mixture of brine and water (1 L, brine/water=1/1). To the resulted organic layer were added sodium sulfate (120 g) and activated carbon (30 g), and the mixture was stirred at room temperature for 1 hour. The mixture was filtered through celite to remove insoluble substances. The insoluble substances were washed with ethyl acetate (3 L). The resulted filtrates were combined and concentrated, and dried under reduced pressure at room temperature for 3 hours to give a crude product of the title compound (561 g).
Separately, the above Organic layer 1 and Organic layer 2 were combined and concentrated. To the residue were added toluene (450 mL) and water (450 mL), and the mixture was separated. The resulted aqueous layer was washed with toluene (450 mL) twice. To the aqueous layer was added ethyl acetate (450 mL). To the mixture was added dropwise 6N hydrochloric acid (70 mL) under ice cooling. To the mixture was added ethyl acetate (300 mL), and the mixture was separated. The resulted aqueous layer was extracted with ethyl acetate (150 mL). The resulted organic layers of ethyl acetate were combined and washed with a mixture of brine and water (225 mL, brine/water=1/1). To the organic layer were added sodium sulfate (30 g) and activated carbon (7.5 g), and the mixture was stirred at room temperature for 1 hour. The mixture was filtered to remove insoluble substances. The insoluble substances were washed with ethyl acetate (750 mL). The resulted filtrates were combined and concentrated, and dried under reduced pressure at room temperature for 3 hours to give a crude product of the title compound (87.3 g).
This crude product was combined with the crude product of the title compound obtained above, and thereto was added CPME (3 L) under nitrogen flow. The mixture was stirred at 120° C. The mixture was slowly cooled to room temperature with stirring for 17 hours 34 minutes. The mixture was cooled with ice and stirred at about 1° C. of the internal temperature for 3 hours. The precipitate was filtered and washed with cooled CPME (900 mL). The precipitate was dried under reduced pressure at 50° C. overnight to give the title compound (585 g) in the total yield of 75% in the 3 steps. The generation of the title compound was confirmed by HPLC analysis and NMR.
The measuring instrument and conditions for HPLC are the same as those in Step 2. The retention time of the title compound was about 3.1 minutes under the measuring conditions for HPLC.
1H-NMR (CDCl3) δ: 1.33 (d, 3H, J=6.5 Hz), 2.68-2.85 (m, 2H), 3.33-3.48 (m, 2H), 3.80 (s, 6H), 4.43 (s, 2H), 6.42-6.46 (m, 2H), 7.11-7.15 (m, 1H).
To (trans)-1-(2,4-dimethoxybenzyl)-4-methyl oxopyrrolidine-3-carboxylic acid (585 g) obtained in Step 3 was added acetonitrile (2.9 L) at room temperature under nitrogen flow. The mixture was stirred at 85° C. To the mixture was added (1R,2R)-(−)-2-amino-1-(4-nitrophenyl)-1,3-propanediol (254 g) over 14 minutes at 85° C. The reaction mixture was stirred at 90° C. for 2 hours 48 minutes. The reaction mixture was cooled to room temperature with stirring overnight. The precipitate was filtered and washed with acetonitrile (2.4 L). The precipitate was dried under ordinary pressure for 8.5 hours at room temperature to give a crude crystal of the title compound (516 g). To the crude crystal were added acetonitrile (2.5 L) and water (0.5 L) at room temperature under nitrogen flow. The mixture was stirred at 100° C. for 1 hour 14 minutes. To the mixture was added dropwise acetonitrile (1.5 L) at 100° C. over 1 hour 7 minutes. The mixture was stirred at 100° C. for 10 minutes. The mixture was cooled to room temperature with stirring for 21 hours 10 minutes. The mixture was stirred for 3 hours 54 minutes under ice cooling. The precipitate was collected by filtration and washed with acetonitrile (1.5 L). The precipitate was dried under ordinary pressure at room temperature for 4 hours to give the title compound (448 g, 99.8% de) in the yield of 45%. The generation of the title compound was confirmed by HPLC analysis.
The measuring instrument and conditions for HPLC are shown as follows.
Measuring instrument: HPLC system, Shimadzu Corporation, High-Performance Liquid Chromatograph Prominence
Measuring conditions:
Column: CHIRAL PAK AD-3R: 3 μm, 150 mm×4.6 mm (Daicel)
Column temperature: 40° C.
Flow rate: 0.50 mL/min.
Time for analysis: 10 min.
Detection wavelength: UV (220 nm)
Mobile phase: (Solution A) 10 mM (sodium) phosphate buffer (pH=2.6), (Solution B) acetonitrile
Delivery of Mobile phase: A mixing ratio (Solution A/Solution B (volume %)) of Solution A and Solution B was maintained 60/40.
The retention time was about 5.6 minutes for (3R,4R)-1-(2,4-dimethoxybenzyl)-4-methyl-5-oxopyrrolidine-3-carboxylic acid and about 6.5 minutes for (3S,4S)-1-(2,4-dimethoxybenzyl)-4-methyl-5-oxopyrrolidine-3-carboxylic acid under the measuring conditions for HPLC.
The conformation of the title compound was determined by X-ray crystallography of its single crystal obtained after recrystallization from methyl isobutyl ketone.
Diastereomeric excess was determined from HPLC area percentages in the measurement results ((3R,4R)/(3S,4S)=99.886%/0.114%).
To a diastereomer salt of (3R,4R)-1-(2,4-dimethoxybenzyl)-4-methyl-5-oxopyrrolidine-3-carboxylic acid with (1R,2R)-(−)-2-amino-1-(4-nitrophenyl)-1,3-propanediol (448 g) obtained in Step 4 were added ethyl acetate (1.8 L) and water (1.34 L) at room temperature. To the mixture was added dropwise 6N hydrochloric acid (168 mL) at room temperature over 16 minutes. The mixture was separated. The resulted aqueous layer was extracted with ethyl acetate (450 mL) three times. The resulted organic layers were combined and washed sequentially with 2N hydrochloric acid (224 mL) and brine (224 mL), and then dried over sodium sulfate (90 g) and concentrated. To the residue was added toluene (220 mL), and the mixture was concentrated. The residue was dried under reduced pressure at room temperature to give the title compound (254 g) in the yield of 98%.
1H-NMR (DMSO-D6) δ: 1.15 (d, 3H, J=7.2 Hz), 2.50-2.58 (m, 1H), 2.73-2.83 (m, 1H), 3.18-3.25 (m, 1H), 3.30-3.38 (m, 1H), 3.75 (s, 3H), 3.77 (s, 3H), 4.19-4.35 (m, 2H), 6.48 (dd, 1H, J=8.4, 2.3 Hz), 6.56 (d, 1H, J=2.3 Hz), 7.00 (d, 1H, J=8.4 Hz), 12.61 (br s, 1H).
To potassium tert-butoxide (180 g) was added THF (2.55 L) at room temperature under nitrogen flow. To the mixture was added dropwise triethyl phosphonoacetate (314 g) over 13 minutes under ice cooling. The dropping funnel used was washed with THF (511 mL), and the washings were added to the reaction mixture. The reaction mixture was stirred for 2 hours 9 minutes under ice cooling. To the reaction mixture was added dropwise ethyl 2-bromopropionate (247 g) over 20 minutes under ice cooling. The dropping funnel used was washed with THF (79 mL), and the washings were added to the reaction mixture. The reaction mixture was stirred at room temperature for 22 hours 45 minutes. To the reaction mixture was added potassium carbonate (188 g) over one minute under ice cooling. To the reaction mixture was added dropwise 37% by weight of aqueous formaldehyde solution (152 mL) over 10 minutes under ice cooling. The reaction mixture was stirred at room temperature for 19 hours 44 minutes. To the reaction mixture was added water (1.57 L) over one minute at room temperature. The reaction mixture was stirred at room temperature for 1 hour 48 minutes. The reaction mixture was separated. The resulted aqueous layer was extracted with THF (200 mL) twice. The resulted organic layers were combined and concentrated. To the residue were added toluene (471 mL) and brine (471 mL). The reaction mixture was stirred and separated. The organic layer was dried over sodium sulfate (63 g). Sodium sulfate was filtered off. Separately, a similar reaction was performed with triethyl phosphonoacetate (300 g) to give a filtrate, which was then combined with the filtrate obtained above to give a solution of the title compound (equivalent to 2.66 mol) in toluene (about 921 mL). The resulted solution of the title compound in toluene was deemed to afford the yield of 100% and used in the next step. The generation of the title compound was confirmed by HPLC analysis.
The measuring instrument and conditions for HPLC are shown as follows.
Measuring instrument: HPLC system, Shimadzu Corporation, High-Performance Liquid Chromatograph Prominence
Measuring conditions:
Column: Kinetex C18: 2.6 μm, 50 mm×2.1 mm (Phenomenex)
Column temperature: 40° C.
Flow rate: 0.4 mL/min.
Time for analysis: 10 min.
Detection wavelength: UV (220 nm)
Mobile phase: (Solution A) water, (Solution B) acetonitrile
Delivery of mobile phase: A mixing ratio (Solution A/Solution B (volume %)) of Solution A and Solution B was maintained 80/20 from 0 minute to 0.01 minute after injection, changed linearly from 80/20 to 10/90 from 0.01 minute to 7 minutes, maintained 10/90 from 7 minutes to 8 minutes, changed linearly from 10/90 to 80/20 from 8 minutes to 9 minutes, and maintained 80/20 from 9 minutes to 10 minutes.
The retention time of the title compound was about 3.7 minutes under the measuring conditions for HPLC.
To a solution of diethyl 2-methyl-3-methylenesuccinate (equivalent to 2.66 mol) obtained in Step 1 in toluene (about 921 mL) was added dropwise 2,4-dimethoxybenzylamine (468 g) over 2 minutes at room temperature under nitrogen flow. The reaction mixture was stirred at 120° C. for 5 hours 45 minutes. The reaction mixture was let stand for a weekend at room temperature. The reaction mixture was cooled with ice to about 15° C. of the internal temperature. To the reaction mixture was added dropwise 2N hydrochloric acid (1.33 L), and the mixture was stirred. The reaction mixture was separated. The resulted aqueous layer was extracted with toluene (150 mL). The resulted organic layers were combined, washed with a mixed solution of brine and water (600 mL, brine/water=1/1), dried over sodium sulfate (120 g), concentrated, and dried under reduced pressure at room temperature overnight to give a crude product of the title compound (790 g; cis/trans=about 1/1, 5.5% by weight of toluene inclusive). The generation of the title compound was confirmed by HPLC analysis.
The measuring instrument and conditions for HPLC are shown as follows.
Measuring instrument: HPLC system, Shimadzu Corporation, High-Performance Liquid Chromatograph Prominence
Measuring conditions:
Column: Atlantis T3: 5 μm, 150 mm×4.6 mm (Waters)
Column temperature: 40° C.
Flow rate: 1.15 mL/min.
Time for analysis: 18 min.
Detection wavelength: UV (220 nm)
Mobile phase: (Solution A) 10 mM (sodium) phosphate buffer (pH=2.6), (Solution B) acetonitrile
Delivery of Mobile phase: A mixing ratio (Solution A/Solution B (volume %)) of Solution A and Solution B was maintained 60/40 from 0 minute to 0.5 minute after injection, changed linearly from 60/40 to 10/90 from 0.5 minute to 8 minutes, maintained 10/90 from 8 minutes to 12.5 minutes, changed linearly from 10/90 to 60/40 from 12.5 minutes to 13.5 minutes, and maintained 60/40 from 13.5 minutes to 18 minutes.
The retention time was about 6.6 minutes for ethyl (cis)-1-(2,4-dimethoxybenzyl)-4-methyl-5-oxopyrrolidine-3-carboxylate and about 6.9 minutes for ethyl (trans)-1-(2,4-dimethoxybenzyl)-4-methyl-5-oxopyrrolidine-3-carboxylate under the measuring conditions for HPLC.
To a crude mixture (790 g, 5.5% by weight of toluene inclusive) of ethyl (cis)-1-(2,4-dimethoxybenzyl)-4-methyl-5-oxopyrrolidine-3-carboxylate and ethyl (trans)-1-(2,4-dimethoxybenzyl)-4-methyl-5-oxopyrrolidine-3-carboxylate, obtained in Step 2, was added ethanol (1.15 L) at room temperature under nitrogen flow. To the reaction mixture was added dropwise sodium ethoxide (20% by weight solution in ethanol, 1.15 L) at room temperature over 31 minutes. The reaction mixture was stirred at room temperature for 2 hours 57 minutes. The reaction mixture was cooled with ice, and thereto was added dropwise water (1.84 L) over 33 minutes. To the reaction mixture were added CPME (1.8 L) and toluene (1.8 L) at room temperature, and the mixture was separated (Organic layer 1). To the resulted aqueous layer was added CPME (1.8 L), and the mixture was separated (Organic layer 2). Solvent (1.8 L) was removed from the resulted aqueous layer by evaporation. To the resulted aqueous layer was added dropwise 6N hydrochloric acid (110 mL) under ice cooling, and thereto was added ethyl acetate (1.8 L). To the mixture was added dropwise 6N hydrochloric acid (300 mL) under ice cooling, and the mixture was stirred for about 10 minutes. To the mixture were sequentially added water (2.2 L), 6N hydrochloric acid (50 mL), water (1.0 L), 10% by weight of aqueous sodium hydrogen sulfate solution (300 mL), and ethanol (300 mL) under ice cooling. The mixture was stirred at room temperature overnight. To the mixture was added ethyl acetate (600 mL), and the mixture was separated. The resulted aqueous layer was extracted with ethyl acetate (600 mL) twice. The resulted organic layers were combined (except for Organic layer 1 and Organic layer 2) and washed with a mixture of brine and water (1 L, brine/water=1/1). To the resulted organic layer were added sodium sulfate (120 g) and activated carbon (30 g), and the mixture was stirred at room temperature for 1 hour. The mixture was filtered through celite to remove insoluble substances. The insoluble substances were washed with ethyl acetate (3 L). The resulted filtrates were combined and concentrated, and dried under reduced pressure at room temperature for 3 hours to give a crude product of the title compound (561 g).
Separately, the above Organic layer 1 and Organic layer 2 were combined and concentrated. To the residue were added toluene (450 mL) and water (450 mL), and the mixture was separated. The resulted aqueous layer was washed with toluene (450 mL) twice. To the aqueous layer was added ethyl acetate (450 mL). To the mixture was added dropwise 6N hydrochloric acid (70 mL) under ice cooling. To the mixture was added ethyl acetate (300 mL), and the mixture was separated. The resulted aqueous layer was extracted with ethyl acetate (150 mL). The resulted organic layers of ethyl acetate were combined and washed with a mixture of brine and water (225 mL, brine/water=1/1). To the organic layer were added sodium sulfate (30 g) and activated carbon (7.5 g), and the mixture was stirred at room temperature for 1 hour. The mixture was filtered to remove insoluble substances. The insoluble substances were washed with ethyl acetate (750 mL). The resulted filtrates were combined and concentrated, and dried under reduced pressure at room temperature for 3 hours to give a crude product of the title compound (87.3 g).
This crude product was combined with the crude product of the title compound obtained above, and thereto was added CPME (3 L) under nitrogen flow. The mixture was stirred at 120° C. The mixture was slowly cooled to room temperature with stirring for 17 hours 34 minutes. The mixture was cooled with ice and stirred at about 1° C. of the internal temperature for 3 hours. The precipitate was filtered and washed with cooled CPME (900 mL). The precipitate was dried under reduced pressure at 50° C. overnight to give the title compound (585 g) in the total yield of 75% in the 3 steps. The generation of the title compound was confirmed by HPLC analysis and NMR.
The measuring instrument and conditions for HPLC are the same as those in Step 2. The retention time of the title compound was about 3.1 minutes under the measuring conditions for HPLC.
1H-NMR (CDCl3) δ: 1.33 (d, 3H, J=6.5 Hz), 2.68-2.85 (m, 2H), 3.33-3.48 (m, 2H), 3.80 (s, 6H), 4.43 (s, 2H), 6.42-6.46 (m, 2H), 7.11-7.15 (m, 1H).
To (trans)-1-(2,4-dimethoxybenzyl)-4-methyl-5-oxopyrrolidine-3-carboxylic acid (585 g) obtained in Step 3 was added acetonitrile (2.9 L) at room temperature under nitrogen flow. The mixture was stirred at 85° C. To the mixture was added (1R,2R)-(−)-2-amino-1-(4-nitrophenyl)-1,3-propanediol (254 g) over 14 minutes at 85° C. The reaction mixture was stirred at 90° C. for 2 hours 48 minutes. The reaction mixture was cooled to room temperature with stirring overnight. The precipitate was filtered and washed with acetonitrile (2.4 L). The precipitate was dried under ordinary pressure for 8.5 hours at room temperature to give a crude crystal of the title compound (516 g). To the crude crystal were added acetonitrile (2.5 L) and water (0.5 L) at room temperature under nitrogen flow. The mixture was stirred at 100° C. for 1 hour 14 minutes. To the mixture was added dropwise acetonitrile (1.5 L) at 100° C. over 1 hour 7 minutes. The mixture was stirred at 100° C. for 10 minutes. The mixture was cooled to room temperature with stirring for 21 hours 10 minutes. The mixture was stirred for 3 hours 54 minutes under ice cooling. The precipitate was collected by filtration and washed with acetonitrile (1.5 L). The precipitate was dried under ordinary pressure at room temperature for 4 hours to give the title compound (448 g, 99.8% de) in the yield of 45%. The generation of the title compound was confirmed by HPLC analysis.
The measuring instrument and conditions for HPLC are shown as follows.
Measuring instrument: HPLC system, Shimadzu Corporation, High-Performance Liquid Chromatograph Prominence
Measuring conditions:
Column: CHIRAL PAK AD-3R: 3 μm, 150 mm×4.6 mm (Daicel)
Column temperature: 40° C.
Flow rate: 0.50 mL/min.
Time for analysis: 10 min.
Detection wavelength: UV (220 nm)
Mobile phase: (Solution A) 10 mM (sodium) phosphate buffer (pH=2.6), (Solution B) acetonitrile
Delivery of Mobile phase: A mixing ratio (Solution A/Solution B (volume %)) of Solution A and Solution B was maintained 60/40.
The retention time was about 5.6 minutes for (3R,4R)-1-(2,4-dimethoxybenzyl)-4-methyl-5-oxopyrrolidine-3-carboxylic acid and about 6.5 minutes for (3S,4S)-1-(2,4-dimethoxybenzyl)-4-methyl-5-oxopyrrolidine-3-carboxylic acid under the measuring conditions for HPLC.
The conformation of the title compound was determined by X-ray crystallography of its single crystal obtained after recrystallization from methyl isobutyl ketone.
Diastereomeric excess was determined from HPLC area percentages in the measurement results ((3R,4R)/(3S,4S)=99.886%/0.114%).
To a diastereomer salt of (3R,4R)-1-(2,4-dimethoxybenzyl)-4-methyl-5-oxopyrrolidine-3-carboxylic acid with (1R,2R)-(−)-2-amino-1-(4-nitrophenyl)-1,3-propanediol (448 g) obtained in Step 4 were added ethyl acetate (1.8 L) and water (1.34 L) at room temperature. To the mixture was added dropwise 6N hydrochloric acid (168 mL) at room temperature over 16 minutes. The mixture was separated. The resulted aqueous layer was extracted with ethyl acetate (450 mL) three times. The resulted organic layers were combined and washed sequentially with 2N hydrochloric acid (224 mL) and brine (224 mL), and then dried over sodium sulfate (90 g) and concentrated. To the residue was added toluene (220 mL), and the mixture was concentrated. The residue was dried under reduced pressure at room temperature to give the title compound (254 g) in the yield of 98%.
1H-NMR (DMSO-D6) δ: 1.15 (d, 3H, J=7.2 Hz), 2.50-2.58 (m, 1H), 2.73-2.83 (m, 1H), 3.18-3.25 (m, 1H), 3.30-3.38 (m, 1H), 3.75 (s, 3H), 3.77 (s, 3H), 4.19-4.35 (m, 2H), 6.48 (dd, 1H, J=8.4, 2.3 Hz), 6.56 (d, 1H, J=2.3 Hz), 7.00 (d, 1H, J=8.4 Hz), 12.61 (br s, 1H).
To a mixture of (3R,4R)-1-(2,4-dimethoxybenzyl)-4-methyl-5-oxopyrrolidine-3-carboxylic acid (254 g) obtained in Step 5 and the compound (33 g) obtained in a similar manner to Step 5 was added a solution of anisole (160 mL) in trifluoroacetic acid (1.44 L) at room temperature under nitrogen flow. The reaction mixture was stirred at 80° C. for 4 hours 4 minutes. The reaction mixture was cooled to room temperature under water cooling. The reaction mixture was concentrated. To the residue was added toluene (287 mL), and the mixture was concentrated. The residue was let stand overnight at room temperature. To the residue was added toluene (287 mL), and the mixture was concentrated. To the residue was added toluene (80 mL) at room temperature. To the mixture was added diisopropyl ether (2.9 L) under water cooling. The mixture was stirred under water cooling. The precipitated solid from the mixture was collected by filtration and washed with diisopropyl ether (431 mL). The solid was dried at room temperature under ordinary pressure to give the title compound (137 g) in the yield of 98%.
1H-NMR (DMSO-D6) δ: 1.10 (d, 3H, J=7.2 Hz), 2.35-2.44 (m, 1H), 2.79-2.87 (m, 1H), 3.19-3.25 (m, 1H), 3.34-3.40 (m, 1H), 7.64 (s, 1H), 12.56 (s, 1H).
To a solution of 5-fluoropyridin-3-amine (1.5 g) in 6N hydrochloric acid (15 mL) was added dropwise a solution of sodium nitrite (0.923 g) in water (7.5 mL) at 0° C. over two minutes. The reaction mixture was stirred at 0° C. for 1 hour 7 minutes. To the reaction mixture was added dropwise a suspension of tin (II) chloride (6.34 g) in 6N hydrochloric acid (15 mL) at 0° C. over 3 minutes. The reaction mixture was stirred at 0° C. for 30 minutes and stirred at room temperature for 23 hours. To the reaction mixture was added dropwise 8N aqueous sodium hydroxide solution (about 34 mL) at 0° C. The mixture was stirred at 0° C. The mixture was extracted with ethyl acetate eight times. The resulted organic layers were combined and washed with brine, dried over sodium sulfate, and concentrated. To the resulted residue was added a mixed solution of methyl tert-butyl ether (6 mL)/n-hexane (36 mL) at room temperature. The resulted suspension was stirred at room temperature. Solid was collected from the suspension by filtration and washed with n-hexane. The solid was dried under reduced pressure at 60° C. to give the title compound (965.8 mg) in the yield of 57%.
1H-NMR (CDCl3) δ: 3.64 (br s, 2H), 5.41 (br s, 1H), 6.99 (dt, 1H, J=10.8, 2.5 Hz), 7.89 (d, 1H, J=2.5 Hz), 7.97-7.99 (m, 1H).
To a solution of 5-(trifluoromethyl)pyridin-3-amine (3 g) in 6N hydrochloric acid (30 mL) was added dropwise a solution of sodium nitrite (1.277 g) in water (15 mL) at 0° C. over two minutes. The reaction mixture was stirred at 0° C. for 1 hour. To the reaction mixture was added dropwise a suspension of tin (II) chloride (8.77 g) in 6N hydrochloric acid (30 mL) at 0° C. over three minutes. The reaction mixture was stirred at 0° C. for 28 minutes and stirred at room temperature for 20 hours 9 minutes. To the reaction mixture was added dropwise 8N aqueous sodium hydroxide solution (about 68 mL) at 0° C. The mixture was stirred at 0° C. The mixture was extracted with ethyl acetate three times. The resulted organic layers were combined and washed with brine, dried over sodium sulfate, and concentrated. To the resulted residue was added a seed crystal of the title compound separately synthesized in a similar manner to the present step. To the mixture was added a mixture of diisopropyl ether (2 mL)/n-hexane (30 mL) at room temperature. This resulted suspension was stirred at room temperature. Solid was collected from the suspension by filtration and washed with n-hexane. The solid was dried under reduced pressure at room temperature to give the title compound (2.8464 g) in the yield of 87%.
1H-NMR (CDCl3) δ: 3.69 (br s, 2H), 5.49 (br s, 1H), 7.43-7.45 (m, 1H), 8.28-8.30 (m, 1H), 8.34 (d, 1H, J=2.8 Hz).
The seed crystal of the title compound used in Step 1 was obtained by purification with silica gel column chromatography (eluent: n-hexane/ethyl acetate=1/1) of the residue obtained in a similar reaction to the present step.
To 5-bromo-2-(trifluoromethyl)pyrimidine (2 g) were added hydrazine monohydrate (4.27 mL) and 2-propanol (1 mL) under argon atmosphere. The reaction mixture was stirred at 95° C. for 22 hours while being protected with an explosion-proof shield. The reaction mixture was cooled to room temperature. To the reaction mixture were added water and saturated aqueous sodium hydrogen carbonate solution, and the mixture was extracted with ethyl acetate five times. The resulted organic layers were combined and washed with brine, dried over sodium sulfate, and concentrated. To the residue was added a mixed solution of n-hexane/ethyl acetate (3/1) at room temperature. The resulted suspension was stirred at room temperature. Solid was collected from the suspension by filtration and washed with a mixed solution of n-hexane/ethyl acetate (3/1). The solid was dried under reduced pressure at room temperature to give the title compound (647 mg) in the yield of 41%.
1H-NMR (DMSO-D6) δ: 4.43 (br s, 2H), 7.94 (br s, 1H), 8.33 (s, 2H).
To 1H-pyrazol-3-amine (100 g) was added acetic acid (1 L) at room temperature, and the mixture was stirred for 5 minutes. To the mixture was added 2,5-hexanedione (148 mL) at room temperature, and the mixture was stirred for 5 minutes. The reaction mixture was stirred at 120° C. for 2.5 hours and cooled to room temperature. To the reaction mixture was added water (1 L) at room temperature. The reaction mixture was stirred at room temperature for 50 minutes. The precipitated solid was collected by filtration and washed with water (1 L). The resulted wet solid was dried under ordinary pressure at room temperature overnight, and then dried under reduced pressure at 65° C. for 3 days and 8.5 hours to give the title compound (172.47 g) in the yield of 89%.
1H-NMR (CDCl3) δ: 2.11 (s, 6H), 5.90 (s, 2H), 6.25 (d, 1H, J=2.4 Hz), 7.51 (d, 1H, J=2.4 Hz).
DMF (100 mL) was added to sodium hydride (14.9 g) under argon flow under ice cooling. To the mixture was added dropwise a suspension of 3-(2,5-dimethyl-1H-pyrrol-1-yl)-1H-pyrazole (40 g) obtained in Step 1 in DMF (150 mL) under ice cooling over 20 minutes. The dropping funnel used was washed with DMF (50 mL) and the washings were added to the reaction mixture. The reaction mixture was stirred under water cooling for 1.5 hours. To the reaction mixture was added tetrabutylammonium bromide (0.80 g) under ice cooling. The reaction mixture was stirred under ice cooling for 15 minutes. To the reaction mixture was added dropwise a solution of dibromodifluoromethane (45 mL) in DMF (50 mL) under ice cooling over 15 minutes. The reaction mixture was stirred under water cooling for 2 hours and 10 minutes. To the reaction mixture was added dropwise dibromodifluoromethane (20 mL) under argon atmosphere under water cooling. The reaction mixture was stirred under water cooling for 40 minutes, and then let stand overnight. To the reaction mixture was added saturated aqueous ammonium chloride solution (200 mL) under ice cooling. To the reaction mixture were added ethyl acetate and water. The reaction mixture was filtered through celite and the filtrate was separated. The resulted aqueous layer was extracted with ethyl acetate. The resulted organic layers were combined, and brine was added thereto. The mixture was filtered through celite and the filtrate was separated. The resulted aqueous layer was extracted with ethyl acetate. The resulted organic layers were combined, and then dried over sodium sulfate and concentrated. Toluene (250 mL) was added to the residue, and the mixture was concentrated. This procedure was repeated. Ethyl acetate (about 150 mL) was added to the residue, and the insoluble substances were filtered off. The insoluble substances were washed with ethyl acetate. The resulted filtrates were combined and concentrated. The residue was dried under reduced pressure with stirring at room temperature for 10 minutes. The residue was purified by silica gel column chromatography (eluent: n-hexane/ethyl acetate=30/1 to 20/1) to give the title compound (40.6 g, 3.7% by weight of hexane inclusive, 1-(bromodifluoromethyl)-3-(2,5-dimethyl-1H-pyrrol-1-yl)-1H-pyrazole:1-(bromodifluoromethyl)-5-(2,5-dimethyl-1H-pyrrol-1-yl)-1H-pyrazole=about 3:1) in the yield of 54%.
1H-NMR (CDCl3) δ: 2.03 (s, 1.5H), 2.18 (s, 4.5H), 5.89 (s, 1.5H), 5.91 (s, 0.5H), 6.39-6.41 (m, 1H), 7.86-7.88 (m, 1H).
To a solution of a mixture of 1-(bromodifluoromethyl)-3-(2,5-dimethyl-1H-pyrrol-1-yl)-1H-pyrazole and 1-(bromodifluoromethyl)-5-(2,5-dimethyl-1H-pyrrol-1-yl)-1H-pyrazole (40.6 g, 3.7% by weight of hexane inclusive) obtained in Step 2 in sulfolane (400 mL) was added tetramethylammonium fluoride (13.0 g) at room temperature under argon flow. The reaction mixture was stirred at 100° C. for 1 hour. To the reaction mixture was added tetramethylammonium fluoride (9.4 g) at 100° C. The reaction mixture was stirred at 100° C. for 1 hour 15 minutes. To the reaction mixture was added tetramethylammonium fluoride (10 g) at 100° C. The reaction mixture was stirred at 100° C. for 40 minutes. In addition, to the reaction mixture was added tetramethylammonium fluoride (5 g) at 100° C. The reaction mixture was stirred at 100° C. for 2 hours 5 minutes, and then cooled to room temperature. To the reaction mixture were slowly and sequentially added water (400 mL) and saturated aqueous sodium hydrogen carbonate solution (200 mL) under ice cooling. To the reaction mixture was added a mixed solution of n-hexane/ethyl acetate (2/3) (400 mL). The reaction mixture was filtered through celite and the filtrate was separated. The resulted organic layer was washed with brine. The resulted aqueous layers were combined and extracted with a mixed solution of n-hexane/ethyl acetate (2/3) (300 mL). The organic layer was washed with brine. The resulted organic layers were combined, dried over sodium sulfate, and concentrated. The residue was purified by silica gel column chromatography (eluent: n-hexane/ethyl acetate=30/1 to 25/1) to give the title compound (21.85 g, 3-(2,5-dimethyl-1H-pyrrol-1-yl)-1-(trifluoromethyl)-1H-pyrazole:5-(2,5-dimethyl-1H-pyrrol-1-yl)-1-(trifluoromethyl)-1H-pyrazole=about 6:1, 24.4% by weight of n-hexane inclusive) in the yield of 51%.
1H-NMR (CDCl3) δ: 2.00 (s, 0.86H), 2.16 (s, 5.1H), 5.89 (s, 1.7H), 5.91 (s, 0.29H), 6.40 (d, 0.86H, J=2.8 Hz), 6.42 (d, 0.14H, J=1.6 Hz), 7.83 (d, 0.14H, J=1.6 Hz), 7.87 (d, 0.86H, J=2.8 Hz).
To a solution of a mixture of 3-(2,5-dimethyl-1H-pyrrol-1-yl)-1-(trifluoromethyl)-1H-pyrazole and 5-(2,5-dimethyl-1H-pyrrol-1-yl)-1-(trifluoromethyl)-1H-pyrazole (21.85 g, 24.4% by weight of n-hexane inclusive) obtained in Step 3 in THF (180 mL) was added dropwise a solution of n-butyllithium in n-hexane (1.55M, 51.1 mL) at −70° C. over 5 minutes under argon atmosphere. The reaction mixture was stirred at −70° C. for 25 minutes. To the reaction mixture was added dropwise a solution of iodine (18.3 g) in THF (50 mL) at −70° C. over 5 minutes. The dropping funnel used was washed with THF (10 mL), and the washings were added to the reaction mixture. The reaction mixture was stirred at −70° C. for 30 minutes. To the reaction mixture was added iodine (0.90 g) at −70° C. The reaction mixture was stirred at −70° C. for 0.5 hour. To the reaction mixture were sequentially added water (250 mL) and ethyl acetate (250 mL) at −70° C. The reaction mixture was stirred at room temperature and separated. The organic layer was sequentially washed with 10% by weight of aqueous sodium hydrogen sulfite solution (250 mL) and brine (150 mL), dried over sodium sulfate, and concentrated. The residue was purified by silica gel column chromatography (eluent: n-hexane/ethyl acetate=50/1 to 30/1). Fractions which include the title compound were collected and concentrated. To the residue was added n-hexane. The mixture was concentrated so that the weight of residue became 27.5 g. To the residue was added n-hexane (20 mL). The suspension was stirred at room temperature for 10 minutes. The precipitate was collected by filtration, washed with n-hexane (30 mL), and dried under reduced pressure to give the title compound (17.14 g) in the yield of 67%. Then, the filtrate was concentrated. The residue was crystallized from n-hexane to give the title compound (1.63 g) in the yield of 6.4%.
1H-NMR (CDCl3) δ: 2.15 (s, 6H), 5.88 (s, 2H), 6.60 (s, 1H).
To 3-(2,5-dimethyl-1H-pyrrol-1-yl)-5-iodo (trifluoromethyl)-1H-pyrazole (18.77 g) obtained in Step 4 were sequentially added a mixture of ethanol and water (ethanol/water=2/1, 480 mL), hydroxylamine hydrochloride (73.5 g), and triethylamine (14.7 mL) at room temperature. The reaction mixture was stirred at 100° C. for 38 hours 20 minutes. The reaction mixture was cooled to room temperature, and the ethanol was removed by evaporation. To the reaction mixture was slowly added a solution of sodium hydroxide (42.3 g) in water (130 mL), followed by addition of ethyl acetate (200 mL), under ice cooling. The reaction mixture was stirred, and separated. The resulted aqueous layer was extracted with ethyl acetate (200 mL). The resulted organic layers were combined, washed with brine, dried over sodium sulfate, and concentrated. To the residue were added ethyl acetate (30 mL) and n-hexane (30 mL), and insoluble substances were filtered off. The filtrate was concentrated. The residue was purified by silica gel column chromatography (eluent: n-hexane/ethyl acetate=4/1 to 3/1) to give the title compound (16.27 g, 14% by weight of ethyl acetate inclusive) in the yield of 96%.
1H-NMR (CDCl3) δ: 3.93 (br s, 2H), 6.09 (s, 1H).
To a solution of 5-iodo-1-(trifluoromethyl)-1H-pyrazol-3-amine (80 mg, 14% by weight of ethyl acetate inclusive) obtained in Step 5 in toluene (3 mL) were sequentially added 2-(3-(tert-butoxy)-5-fluorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (127 mg) obtained in Step 2 of Preparation 1, palladium (II) acetate (6.5 mg), and 2-dicyclohexylphosphino-2′,6′-dimethoxybiphenyl (20 mg) at room temperature under argon atmosphere. The reaction mixture was stirred at room temperature for 4 minutes. To the reaction mixture was added 2M aqueous tripotassium phosphate solution (1.5 mL) at room temperature. The reaction mixture was stirred at 90° C. for 47 minutes. The reaction mixture was cooled to room temperature. To the reaction mixture were added ethyl acetate and saturated aqueous sodium hydrogen carbonate solution. The reaction mixture was filtered through cotton and extracted with ethyl acetate. The organic layer was sequentially washed with saturated aqueous sodium hydrogen carbonate solution and brine, dried over sodium sulfate, and concentrated. The residue was combined with a portion of the title compound (15 mg) separately obtained in a similar manner to the present step using 5-iodo-1-(trifluoromethyl)-1H-pyrazol amine (70 mg, 14% by weight of ethyl acetate inclusive) obtained in Step 5, and the mixture was purified by silica gel thin-layer chromatography (eluent: n-hexane/ethyl acetate=3/1) to give the title compound (108 mg).
1H-NMR (CDCl3) δ: 1.36 (s, 9H), 3.93 (br s, 2H), 5.83 (s, 1H), 6.75-6.85 (m, 3H).
To a solution of (3R,4R)-1-(2,4-dimethoxybenzyl)-4-methyl-5-oxopyrrolidine-3-carboxylic acid (55 mg) obtained in a similar manner to Step 5 of Preparation 2 in chloroform (0.55 mL) were sequentially added DMF (1 μL) and oxalyl chloride (33 μL) under ice cooling under argon atmosphere. The reaction mixture was stirred under ice cooling for 50 minutes. The reaction mixture was concentrated and dried under reduced pressure. To the residue were sequentially added chloroform (0.4 mL) and 5-(3-(tert-butoxy) fluorophenyl)-1-(trifluoromethyl)-1H-pyrazol-3-amine (40 mg) obtained in Step 6 under argon atmosphere under ice cooling. To the reaction mixture was added pyridine (50 μL) under ice cooling. The reaction mixture was stirred under ice cooling for 5 minutes and at room temperature for 35 minutes. To the reaction mixture was added saturated aqueous sodium hydrogen carbonate solution at room temperature, and the mixture was extracted with ethyl acetate. The organic layer was washed with brine, dried over sodium sulfate, and concentrated. The residue was purified by silica gel thin-layer chromatography (eluent: n-hexane/ethyl acetate=1/1) to give the title compound (60 mg) in the yield of 80%. The generation of the title compound was confirmed by thin-layer chromatography (eluent: n-hexane/ethyl acetate=2/1, Rf: 0.19).
To (3R,4R)—N-(5-(3-(tert-butoxy)-5-fluorophenyl)-1-(trifluoromethyl)-1H-pyrazol-3-yl)-1-(2,4-dimethoxybenzyl)-4-methyl-5-oxopyrrolidine-3-carboxamide (60 mg) obtained in Step 7 were added anisole (58 μL) and trifluoroacetic acid (2 mL) at room temperature. The reaction mixture was stirred at 80° C. for 1 hour 20 minutes. The reaction mixture was concentrated. To the residue was added saturated aqueous sodium hydrogen carbonate solution, and the mixture was extracted with ethyl acetate. The organic layer was washed with brine, dried over sodium sulfate, and concentrated. The residue was purified by silica gel thin-layer chromatography (eluent: chloroform/ethyl acetate=1/1) to give the title compound (29.9 mg) in the yield of 76%.
1H-NMR (DMSO-d6) δ: 1.06 (d, 3H, J=7.2 Hz), 2.50-2.53 (m, 1H), 2.96-3.04 (m, 1H), 3.17-3.23 (m, 1H), 3.40-3.46 (m, 1H), 6.67-6.81 (m, 3H), 6.96 (s, 1H), 7.67 (s, 1H), 10.34 (s, 1H), 11.26 (s, 1H).
To (3R, 4R)—N-(5-(3-fluoro-5-hydroxyphenyl)-1-(trifluoromethyl)-1H-pyrazol-3-yl)-4-methyl-5-oxopyrrolidine-3-carboxamide (30 mg) obtained in Step 8 were sequentially added di-tert-butyl dicarbonate, chloroform (1 mL) and magnesium perchlorate at room temperature. The reaction mixture was stirred at 55° C. for 0.5 hours. To the reaction mixture was added magnesium perchlorate at 55° C. The reaction mixture was stirred at 55° C. for 1 hour 10 minutes. To the reaction mixture was added the additional magnesium perchlorate at 55° C. The reaction mixture was stirred at 55° C. for 20 minutes. The reaction mixture was cooled to room temperature, and then thereto was added ethyl acetate. The reaction mixture was sequentially washed with 1N hydrochloric acid and brine, dried over sodium sulfate, and concentrated. The residue was purified by silica gel thin-layer chromatography (eluent: chloroform/methanol=15/1) to give the title compound (19.2 mg) in the yield of 56%.
The title compound (100 mg) was stirred in ethanol (0.4 mL) at 65° C. for 8 minutes and dissolved. To the mixed solution was added dropwise water (0.4 mL) at 65° C. over 2 minutes. The mixture was stirred at 65° C. for 10 minutes. The mixture was cooled to 25° C. with stirring over 2 hours. Further, the mixture was stirred at room temperature for 2 hours. The solid precipitated from the mixture was collected by filtration. The obtained solid was washed with a mixed solution of ethanol/water (=1/1) and dried under reduced pressure at 60° C. to give a crystal of the title compound (87.8 mg) in the yield of 88%.
To a solution of 1-bromo-3,5-difluorobenzene (5.97 mL) in 1,3-dimethyl-2-imidazolidinone (10 mL) was added sodium hydride (4.14 g) at room temperature under nitrogen flow. To the resulted mixture was added dropwise 1,1,1-trifluoro-2-methylpropan-2-ol (8 mL) under water cooling. To the reaction mixture was added 1,3-dimethyl-2-imidazolidinone (2 mL) at room temperature. To the reaction mixture was added dropwise 1,1,1-trifluoro-2-methylpropan-2-ol (3.16 mL) at room temperature. It took 45 minutes for the addition of all of these alcohols. This reaction mixture was stirred at room temperature for 20 minutes, at 80° C. for 20 minutes, at 100° C. for 20 minutes, and at 130° C. for 20 hours 40 minutes. To the reaction mixture was added water under ice cooling. The mixture was extracted with n-hexane three times. The resulted organic layers were combined, washed with water three times and brine, dried over sodium sulfate, and concentrated under reduced pressure of 140 mmHg at 35° C. The residue was purified by silica gel column chromatography (eluent: n-hexane/ethyl acetate=100/0 to 0/100) to give the title compound (8.31 g; 12% by weight of n-hexane inclusive) in the yield of 47%.
1H-NMR (DMSO-D6) 5: 1.46 (s, 6H), 7.08 (dt, 1H, J=10.2, 2.1 Hz), 7.18 (s, 1H), 7.39-7.45 (m, 1H).
To a solution of a mixture of 1-bromo-3-fluoro-5-((1,1,1-trifluoro-2-methylpropan-2-yl)oxy)benzene (2.86 g; 12% by weight of n-hexane inclusive) obtained in Step 1 and the compound obtained in a similar manner to Step 1 (10.2 g; 12% by weight of n-hexane inclusive) in ethylene glycol (69 mL) were added butylvinyl ether (19.77 mL), triethylamine (10.65 mL), 1,1′-bis(diphenylphosphino)ferrocene (1.271 g), and palladium (II) acetate (0.257 g) at room temperature. The reaction mixture was stirred at 110° C. under argon atmosphere for 19 hours. The reaction mixture was cooled to room temperature. To the reaction mixture were added water and n-hexane. The mixture was filtered through celite. The resulted filtrate was extracted with n-hexane twice. The resulted organic layers were combined, washed with water twice and brine, dried over magnesium sulfate, and concentrated under reduced pressure of 140 mmHg at 35° C. The residue was purified by silica gel column chromatography (eluent: n-hexane/ethyl acetate=100/0 to 95/5) to give the title compound (6.39 g; 15% by weight of n-hexane inclusive) in the yield of 44%.
1H-NMR (DMSO-D6) δ: 0.95 (t, 3H, J=7.3 Hz), 1.40-1.51 (m, 2H), 1.44 (s, 6H), 1.69-1.76 (m, 2H), 3.84 (t, 2H, J=6.3 Hz), 4.39 (d, 1H, J=3.0 Hz), 4.90 (d, 1H, J=3.0 Hz), 6.96-7.01 (m, 1H), 7.12 (s, 1H), 7.24-7.29 (m, 1H).
To a solution of 1-(1-butoxyvinyl)-3-fluoro-5-((1,1,1-trifluoro-2-methylpropan-2-yl)oxy)benzene (6.39 g; 15% by weight of n-hexane inclusive) obtained in Step 2 in THF (25 mL) was added 2N hydrochloric acid (12.71 mL) at 0° C. The reaction mixture was stirred at room temperature for 1 hour 10 minutes. 2N aqueous sodium hydroxide solution was added to the reaction mixture under ice cooling so as to adjust pH to 12. The mixture was extracted with n-hexane twice. The resulted organic layers were combined, washed with brine twice, dried over sodium sulfate, and concentrated under reduced pressure of 120 mmHg at 35° C. The residue was purified by silica gel column chromatography (eluent: n-hexane/ethyl acetate=98/2 to 85/15) to give the title compound (4.09 g; 6% by weight of n-hexane inclusive) in the yield of 86%.
1H-NMR (DMSO-D6) δ: 1.47 (s, 6H), 2.60 (s, 3H), 7.32 (dt, 1H, J=9.7, 2.3 Hz), 7.42-7.43 (m, 1H), 7.58-7.62 (m, 1H).
To a solution of 1-(3-fluoro-5-((1,1,1-trifluoro-2-methylpropan-2-yl)oxy)phenyl)ethan-1-one (4.09 g; 6% by weight of n-hexane inclusive) obtained in Step 3 in THF (38.4 mL) was added diethyl oxalate (2.171 mL) under argon atmosphere. To the mixture was added lithium tert-butoxide (1.396 g) at 0° C. The reaction mixture was stirred at 0° C. for 3 hours 10 minutes. 1N hydrochloric acid was added to the reaction mixture under ice cooling so as to adjust pH to 1. To the mixture was added water, and the mixture was extracted with ethyl acetate twice. The resulted organic layers were washed with brine twice, and dried over sodium sulfate. The organic layers were concentrated to give the title compound (5.53 g; 4% by weight of diethyl oxalate and 6% by weight of ethyl acetate inclusive) in the yield of 94%.
1H-NMR (CDCl3) δ: 1.42 (t, 3H, J=7.5 Hz), 1.50 (s, 6H), 4.42 (q, 2H, J=7.5 Hz), 6.97 (s, 1H), 7.01 (dt, 1H, J=9.3, 2.2 Hz), 7.42-7.45 (m, 1H), 7.48 (dt, 1H, J=8.8, 2.2 Hz), 15.02 (br s, 1H).
To a solution of ethyl 4-(3-fluoro-5-((1,1,1-trifluoro-2-methylpropan-2-yl)oxy)phenyl)-2,4-dioxobutanoate (500 mg; 4% by weight of diethyl oxalate and 6% by weight of ethyl acetate inclusive) obtained in Step 4 in acetic acid (2.25 mL) was added 5-hydrazinyl-2-(trifluoromethyl)pyrimidine (242 mg) obtained in Preparation 6 Step 1 at room temperature under argon atmosphere. The reaction mixture was stirred at 100° C. for 21 hours 30 minutes. The reaction mixture was let stand for a weekend at room temperature. The reaction mixture was concentrated. Acetic acid was removed by azeotropy with toluene three times. The residue was purified by silica gel column chromatography (eluent: n-hexane/ethyl acetate=75/25 to 0/100) to give a crude product of the title compound. To the crude product was added a mixed solution of n-hexane/ethyl acetate (20/1) at room temperature. The resulted suspension was stirred at room temperature. Solid was collected from the suspension by filtration and washed with a mixed solution of n-hexane/ethyl acetate (20/1). The resulted solid was dried under reduced pressure at room temperature to give the title compound (541 mg) in the yield of 86%.
1H-NMR (DMSO-D6) δ: 1.29 (s, 6H), 1.33 (t, 3H, J=7.1 Hz), 4.38 (q, 2H, J=7.1 Hz), 6.83-6.84 (m, 1H), 7.13 (dt, 1H, J=10.0, 2.3 Hz), 7.31-7.35 (m, 1H), 7.39 (s, 1H), 9.12 (s, 2H).
To a solution of ethyl 5-(3-fluoro-5-((1,1,1-trifluoro-2-methylpropan-2-yl) oxy) phenyl)-1-(2-(trifluoromethyl) pyrimidin-5-yl)-1H-pyrazole-3-carboxylate (541 mg) obtained in Step 5 in THF (1.623 mL)/methanol (3.246 mL) was added 2N aqueous sodium hydroxide solution (1.068 mL) at room temperature. To the reaction mixture was added methanol (4 mL) at room temperature. The reaction mixture was stirred at room temperature for 25 hours 30 minutes. 1N hydrochloric acid was added to the reaction mixture under ice cooling so as to adjust pH to 1. To the mixture was added water, and the mixture was extracted with ethyl acetate twice. The resulted organic layers were combined, washed with brine twice, and dried over sodium sulfate. The organic layers were concentrated to give the title compound (504 mg) in the yield of 99%.
1H-NMR (DMSO-D6) δ: 1.29 (s, 6H), 6.84 (s, 1H), 7.11-7.15 (m, 1H), 7.30-7.34 (m, 2H), 9.10 (s, 2H), 13.35 (br s, 1H).
To a mixed solution of 5-(3-fluoro-5-((1,1,1-trifluoro-2-methylpropan-2-yl)oxy)phenyl)-1-(2-(trifluoromethyl)pyrimidin-5-yl)-1H-pyrazole-3-carboxylic acid (495 mg) obtained in Step 6 in toluene (4.95 mL) were added triethylamine (0.346 mL) and diphenylphosphoryl azide (0.267 mL) at room temperature under argon atmosphere. The reaction mixture was stirred at room temperature for one hour. To the reaction mixture was added tert-butanol (4.26 mL) at room temperature. The reaction mixture was stirred at 100° C. for 27 hours 15 minutes. The reaction mixture was concentrated. The residue was purified by silica gel column chromatography (eluent: n-hexane/ethyl acetate=99/1 to 50/50) to give the title compound (315 mg) in the yield of 55%.
1H-NMR (DMSO-D6) δ: 1.32 (s, 6H), 1.48 (s, 9H), 6.85 (s, 1H), 6.92 (s, 1H), 7.09-7.14 (m, 1H), 7.27-7.31 (m, 1H), 8.90 (s, 2H), 10.18 (br s, 1H).
To tert-butyl (5-(3-fluoro-5-((1,1,1-trifluoro-2-methylpropan-2-yl)oxy)phenyl)-1-(2-(trifluoromethyl)pyrimidin-5-yl)-1H-pyrazol-3-yl)carbamate (315 mg) obtained in Step 7 was added 4N hydrochloric acid/1,4-dioxane solution (1.575 mL) at 0° C. under argon atmosphere. The reaction mixture was stirred at 0° C. for 10 minutes and at room temperature for 27 hours 40 minutes. The reaction mixture was concentrated. To the residue was added saturated aqueous sodium hydrogen carbonate solution, and the mixture was extracted with ethyl acetate twice. The resulted organic layers were combined, washed with brine, dried over sodium sulfate, and concentrated. The residue was purified by silica gel column chromatography (eluent: n-hexane/ethyl acetate=90/10 to 50/50) to give a solid. To the solid was added a mixed solution of n-hexane/ethyl acetate (10/1) at room temperature. The resulted suspension was stirred at room temperature. Solid was collected from the suspension by filtration and washed with a mixed solution of n-hexane/ethyl acetate (10/1). The resulted solid was dried under reduced pressure at room temperature to give the title compound (224 mg) in the yield of 87%.
1H-NMR (DMSO-D6) δ: 1.34 (s, 6H), 5.50 (br s, 2H), 6.11 (s, 1H), 6.82-6.85 (m, 1H), 7.10 (dt, 1H, J=10.1, 2.3 Hz), 7.21-7.26 (m, 1H), 8.76 (s, 2H).
To a solution of 5-(3-fluoro-5-((1,1,1-trifluoro methylpropan-2-yl)oxy)phenyl)-1-(2-(trifluoromethyl)pyrimidin-5-yl)-1H-pyrazol-3-amine (60 mg) obtained in Step 8 and (3R,4R)-4-methyl-5-oxopyrrolidine carboxylic acid (21.0 mg) obtained in a similar manner to Preparation 3 Step 6 in pyridine (1 mL) was added WSC.HCl (28.2 mg) at room temperature under argon atmosphere. The reaction mixture was stirred at room temperature for 29 hours. The reaction mixture was concentrated. To the residue was added water, and the mixture was extracted with ethyl acetate. The resulted organic layer was washed sequentially with 1N hydrochloric acid twice, water, saturated aqueous sodium hydrogen carbonate solution, and brine, dried over sodium sulfate, and concentrated. The residue was purified by silica gel thin-layer chromatography (eluent: ethyl acetate/methanol=50/1) to give the title compound (69 mg; 4% by weight of ethyl acetate and 1% by weight of n-hexane inclusive) in the yield of 86%.
1H-NMR (DMSO-D6) δ: 1.09 (d, 3H, J=7.2 Hz), 1.32 (s, 6H), 2.50-2.59 (m, 1H), 3.03-3.11 (m, 1H), 3.20-3.27 (m, 1H), 3.43-3.50 (m, 1H), 6.85-6.87 (m, 1H), 7.13 (dt, 1H, J=9.9, 2.3 Hz), 7.17 (s, 1H), 7.27-7.32 (m, 1H), 7.68 (s, 1H), 8.95 (s, 2H), 11.20 (br s, 1H).
MS (M+H) 575, MS (M−H) 573
To a solution of 1-(3-fluoro-5-(trifluoromethoxy)phenyl)ethan-1-one (5 g) and dibenzyl oxalate (6.69 g) in THF (50 mL) was added lithium tert-butoxide (1.982 g) under ice cooling under argon atmosphere. The reaction mixture was stirred for 1 hour under ice cooling. To the reaction mixture were added 2N hydrochloric acid (12.5 mL), ethyl acetate, and water under ice cooling. The mixture was separated. The resulted organic layers were washed with brine and dried over sodium sulfate. The organic layers were concentrated to give a crude product of the title compound (11.7 g).
To a solution of the crude product of benzyl 4-(3-fluoro-5-(trifluoromethoxy)phenyl)-2,4-dioxobutanoate (800 mg) obtained in Step 1 in acetic acid (6 mL) was added 3-fluoro-5-hydrazinylpyridine (218 mg) obtained in Preparation 4 Step 1 at room temperature under argon atmosphere. The reaction mixture was stirred at 100° C. for 19 hours 42 minutes. The reaction mixture was cooled to room temperature and concentrated. To the residue was added toluene, and the mixture was concentrated. The residue was purified by silica gel column chromatography (eluent: n-hexane/ethyl acetate=90/10 to 69/31) to give the title compound (589.5 mg) in the yield of 79% for the two step.
1H-NMR (CDCl3) δ: 5.44 (s, 2H), 6.83-6.86 (m, 1H), 6.93 (ddd, 1H, J=8.4, 2.3, 1.6 Hz), 6.99-7.03 (m, 1H), 7.12 (s, 1H), 7.34-7.42 (m, 3H), 7.46-7.50 (m, 2H), 7.60 (ddd, 1H, J=8.6, 2.5, 1.8 Hz), 8.32 (d, 1H, J=1.8 Hz), 8.53 (d, 1H, J=2.5 Hz).
To a solution of benzyl 5-(3-fluoro-5-(trifluoromethoxy)phenyl)-1-(5-fluoropyridin-3-yl)-1H-pyrazole-3-carboxylate (589.5 mg) obtained in Step 2 in ethyl acetate (5.90 mL) was added 5% by weight of palladium carbon (88 mg) at room temperature under argon atmosphere. The reaction mixture was stirred at room temperature for two hours under 1 atm of hydrogen atmosphere. The hydrogen atmosphere was replaced with nitrogen, and then palladium carbon in the reaction solution was removed by filtration through celite. The celite used was washed with a mixed solution of ethyl acetate/methanol (9/1). The resulted filtrate were combined and concentrated. To the resulted residue was added toluene, and the mixture was concentrated. The residue was dried under reduced pressure at room temperature to give the title compound (425.9 mg) in the yield of 89%.
1H-NMR (DMSO-D6) δ: 7.06-7.09 (m, 1H), 7.33 (s, 1H), 7.45 (ddd, 1H, J=9.2, 2.4, 1.5 Hz), 7.47-7.52 (m, 1H), 7.96 (ddd, 1H, J=9.2, 2.5, 2.1 Hz), 8.44-8.47 (m, 1H), 8.73 (d, 1H, J=2.5 Hz), 13.23 (br s, 1H).
To a solution of 5-(3-fluoro-5-(trifluoromethoxy)phenyl)-1-(5-fluoropyridin-3-yl)-1H-pyrazole-3-carboxylic acid (425.9 mg) obtained in Step 3 and triethylamine (0.370 mL) in tert-butanol (4.26 mL)/toluene (8.52 mL) was added diphenylphosphoryl azide (0.286 mL) at room temperature under argon atmosphere. The reaction mixture was stirred at 110° C. for 14 hours 50 minutes. The reaction mixture was cooled to room temperature and concentrated. To the residue was added water, and the mixture was extracted with ethyl acetate. The resulted organic layers were washed with brine, dried over sodium sulfate, and concentrated. To the residue was added a mixed solution of n-hexane/ethyl acetate (1/1) at room temperature. The resulted suspension was stirred at room temperature. The resulted insoluble substance was collected by filtration and washed with a mixed solution of n-hexane/ethyl acetate (1/1). The resulted filtrate were combined and concentrated. The residue was purified by silica gel column chromatography (eluent: n-hexane/ethyl acetate=90/10 to 69/31) to give the title compound (207.4 mg) in the yield of 41%.
1H-NMR (DMSO-D6) δ: 1.48 (s, 9H), 6.90 (s, 1H), 7.06 (s, 1H), 7.40 (ddd, 1H, J=9.1, 2.4, 1.5 Hz), 7.44-7.49 (m, 1H), 7.73 (ddd, 1H, J=9.5, 2.5, 2.1 Hz), 8.32-8.34 (m, 1H), 8.61 (d, 1H, J=2.3 Hz), 10.05 (br s, 1H).
To tert-butyl (5-(3-fluoro (trifluoromethoxy)phenyl)-1-(5-fluoropyridin-3-yl)-1H-pyrazol-3-yl)carbamate (207.4 mg) obtained in Step 4 was added trifluoroacetic acid (2.07 mL) at room temperature under argon atmosphere. The reaction mixture was stirred at room temperature for 22 hours 40 minutes. To the reaction mixture was added water at 0° C. To the mixture was added dropwise 8N aqueous sodium hydroxide solution (about 3.36 mL) at 0° C. To the mixture was added saturated aqueous sodium hydrogen carbonate solution at 0° C. The mixture was extracted with ethyl acetate. The resulted organic layers were washed with brine, dried over sodium sulfate, and concentrated. The residue was purified by silica gel column chromatography (eluent: n-hexane/ethyl acetate=64/36 to 43/57) to give a solid. To the solid was added n-hexane at room temperature. The resulted suspension was stirred at room temperature. Solid was collected from the suspension by filtration and washed with n-hexane. The resulted solid was dried under reduced pressure at 60° C. to give the title compound (100.0 mg; 0.21% by weight of ethyl acetate inclusive) in the yield of 62%.
1H-NMR (CDCl3) δ: 3.89 (br s, 2H), 6.00 (s, 1H), 6.86-6.89 (m, 1H), 6.93 (ddd, 1H, J=8.6, 2.3, 1.4 Hz), 6.96-7.00 (m, 1H), 7.43 (dt, 1H, J=9.2, 2.5 Hz), 8.20-8.22 (m, 1H), 8.36 (d, 1H, J=2.5 Hz).
To a solution of 5-(3-fluoro-5-(trifluoromethoxy)phenyl)-1-(5-fluoropyridin-3-yl)-1H-pyrazol-3-amine (38 mg; 0.21% by weight of ethyl acetate inclusive) obtained in Step 5 and (3R,4R)-4-methyl-5-oxopyrrolidine-3-carboxylic acid (18.3 mg) obtained in a similar manner to Preparation 3 Step 6 in pyridine (0.380 mL) was added WSC.HCl (24.5 mg) at room temperature under argon atmosphere. The reaction mixture was stirred at room temperature for 2 hours 54 minutes. To the reaction mixture were added (3R,4R)-4-methyl-5-oxopyrrolidine-3-carboxylic acid (18 mg) obtained in a similar manner to Preparation 3 Step 6 and WSC.HCl (25 mg) at room temperature. The reaction mixture was stirred at room temperature overnight. To the reaction mixture was added 10% by weight of aqueous solution of citric acid at room temperature, and the mixture was extracted with ethyl acetate. The resulted organic layers were washed with water and brine, dried over sodium sulfate, and concentrated. The residue was purified by silica gel thin-layer chromatography (eluent: ethyl acetate/methanol=97/3) to give the title compound. A mixed solution of n-hexane/ethyl acetate was added to the resulted title compound at room temperature. The resulted suspension was stirred at room temperature. Solid was collected from the suspension by filtration and washed with n-hexane. The resulted solid was dried under reduced pressure at 70° C. to give the title compound (46.6 mg; 3.5% by weight of n-hexane inclusive) in the yield of 87%.
To ((3R,4R)—N-(5-(3-fluoro-5-(trifluoromethoxy)phenyl)-1-(5-fluoropyridin-3-yl)-1H-pyrazol-3-yl)-4-methyl-5-oxopyrrolidine-3-carboxamide (200 mg) was added ethanol (0.6 mL), and the mixture was heated at 60° C. so as to become a solution. This solution was cooled to room temperature. To this solution was added dropwise water (1.2 mL) at room temperature, and the mixture was stirred for 4 hours. The precipitated solid was collected by filtration and washed with a mixed solution of ethanol/water (=1/2). The resulted solid was dried under reduced pressure at 40° C. to give the title compound (192 mg) in the yield of 92%.
Calculated value: C, 50.51 wt %, H, 3.63 wt %, N, 14.02 wt %
Measured value: C, 50.61 wt %, H, 3.46 wt %, N, 13.95 wt %
To a solution of a crude product of benzyl 4-(3-fluoro-5-(trifluoromethoxy)phenyl)-2,4-dioxobutanoate (800 mg) obtained in Example 3 Step 1 in acetic acid (6 mL) was added 3-hydrazinyl-5-(trifluoromethyl)pyridine (304 mg) obtained in Preparation 5 Step 1 at room temperature under argon atmosphere. The reaction mixture was stirred at 100° C. for 22 hours 30 minutes. This reaction mixture was cooled to room temperature and concentrated. To the residue was added toluene, and the mixture was concentrated. This operation was repeated. The residue was purified by silica gel column chromatography (eluent: n-hexane/ethyl acetate=97/3 to 70/30) to give the title compound (640 mg) in the yield of 78% for the two steps.
1H-NMR (CDCl3) δ: 5.45 (s, 2H), 6.80-6.83 (m, 1H), 6.94 (ddd, 1H, J=8.3, 2.3, 1.6 Hz), 7.00-7.05 (m, 1H), 7.14 (s, 1H), 7.33-7.42 (m, 3H), 7.46-7.50 (m, 2H), 8.04-8.07 (m, 1H), 8.69 (d, 1H, J=2.5 Hz), 8.88-8.92 (m, 1H).
To a solution of benzyl 5-(3-fluoro-5-(trifluoromethoxy)phenyl)-1-(5-(trifluoromethyl)pyridin-3-yl)-1H-pyrazole-3-carboxylate (640 mg) obtained in Step 1 in ethyl acetate (6.4 mL) was added 5% by weight of palladium carbon (32 mg) at room temperature. The reaction mixture was stirred under 1 atm of hydrogen atmosphere for 2 hours. The hydrogen atmosphere was replaced with nitrogen, and then THF was added to the reaction mixture. Palladium carbon in the reaction solution was removed by filtration through celite. The celite used was washed with THF. The resulted filtrates were combined and concentrated. To the residue was added n-hexane, and the mixture was concentrated. This operation was repeated. The residue was dried under reduced pressure at room temperature to give a crude product of the title compound (525 mg).
To a solution of a crude product of 5-(3-fluoro-5-(trifluoromethoxy) phenyl)-1-(5-(trifluoromethyl) pyridin-3-yl)-1H-pyrazole-3-carboxylic acid (525 mg) obtained in Step 2 and triethylamine (0.403 mL) in tert-butanol (5 mL)/toluene (10 mL) was added diphenylphosphoryl azide (0.311 mL) at room temperature under argon atmosphere. The reaction mixture was stirred at 100° C. for 16 hours. The reaction mixture was cooled to room temperature and concentrated. The residue was purified by silica gel column chromatography (eluent: n-hexane/ethyl acetate=97/3 to 70/30) to give the title compound (420 mg) in the yield of 68% for the two steps. Generation of the title compound was confirmed by thin-layer chromatography (eluent: n-hexane/ethyl acetate=4/1, Rf value: 0.46).
To tert-butyl (5-(3-fluoro-5-(trifluoromethoxy)phenyl)-1-(5-(trifluoromethyl)pyridin-3-yl)-1H-pyrazol-3-yl)carbamate (420 mg) obtained in Step 3 was added trifluoroacetic acid (3 mL) at room temperature. The reaction mixture was stirred at room temperature for 1 hour 30 minutes. The reaction mixture was concentrated. To the residue was added toluene, and the mixture was concentrated. This operation was repeated. To the residue were added ethyl acetate and saturated aqueous sodium hydrogen carbonate solution. The resulted mixed solution was separated. The resulted organic layer was washed with brine, dried over sodium sulfate, and concentrated. The residue was purified by silica gel column chromatography (eluent: n-hexane/ethyl acetate=92/8 to 20/80) to give the title compound (313 mg) in the yield of 93%.
1H-NMR (CDCl3) δ: 3.92 (br s, 2H), 6.03 (s, 1H), 6.84-6.87 (m, 1H), 6.94 (ddd, 1H, J=8.4, 2.2, 1.3 Hz), 6.97-7.02 (m, 1H), 7.87-7.90 (m, 1H), 8.57 (d, 1H, J=2.4 Hz), 8.71-8.74 (m, 1H).
To a solution of 5-(3-fluoro-5-(trifluoromethoxy)phenyl)-1-(5-(trifluoromethyl)pyridin-3-yl)-1H-pyrazol-3-amine (60 mg) obtained in Step 4 and (3R,4R)-4-methyl-5-oxopyrrolidine-3-carboxylic acid (23.3 mg) obtained in a similar manner to Preparation 3 Step 6 in pyridine (1 mL) was added WSC.HCl (31.1 mg) at room temperature. The reaction mixture was stirred at room temperature for 15 hours 30 minutes. To the reaction mixture were added water and ethyl acetate at room temperature. The resulted mixed solution was separated. The resulted organic layer was washed with brine, dried over sodium sulfate, and concentrated. To the residue was added toluene, and the mixture was concentrated. This operation was repeated. The residue was purified by silica gel thin-layer chromatography (eluent: ethyl acetate) to give the title compound (75 mg) in the yield of 96%.
In accordance with similar manners to the above General Preparations, Preparations and Examples, and if needed, other known methods, other Example compounds were obtained. Structures and physical property data of compounds of Examples 1 to 40 are shown in the following table.
1H-NMR
1H-NMR (DMSO-D6) δ: 1.08 (d, 3H, J =
1H-NMR (DMSO-D6) δ: 1.09 (d, 3H, J =
1H-NMR (DMSO-D6) δ: 1.09 (d, 3H, J =
1H-NMR (DMSO-D6) δ: 1.09 (d, 3H, J =
1H-NMR (CDCl3) δ: 1.35 (d, 3H, J= 6.9
1H-NMR (DMSO-D6) δ: 1.09 (d, 3H, J =
1H-NMR (DMSO-D6) δ: 1.09 (d, 3H, J =
1H-NMR (DMSO-D6) δ: 1.09 (d, 3H, J =
1H-NMR (DMSO-D6) δ: 1.09 (d, 3H, J =
1H-NMR (DMSO-D6) δ: 1.09 (d, 3H, J =
1H-NMR (DMSO-D6) δ: 1.10 (d, 3H, J =
1H-NMR (DMSO-D6) δ: 1.09 (d, 3H, J =
1H-NMR (CDCl3) δ: 1.34 (d, 3H, J= 6.9
1H-NMR (CDCl3) δ: 1.28 (s, 6H), 1.33
1H-NMR (DMSO-D6) δ: 1.08 (d, 3H, J =
1H-NMR (CDCl3) δ: 1.33-1.39 (m, 9H),
1H-NMR (DMSO-D6) δ: 1.10 (d, 3H, J =
1H-NMR (DMSO-D6) δ: 1.09 (d, 3H, J =
1H-NMR (DMSO-D6) δ: 1.09 (d, 3H, J =
1H-NMR (DMSO-D6) δ: 1.10 (d, 3H, J =
1H-NMR (DMSO-D6) δ: 1.09 (d, 3H, J =
1H-NMR (DMSO-D6) δ: 1.09 (d, 3H, J =
1H-NMR (DMSO-D6) δ: 1.09 (d, 3H, J =
1H-NMR (DMSO-D6) δ: 1.09 (d, 3H, J =
1H-NMR (DMSO-D6) δ: 1.08 (d, 3H, J =
1H-NMR (DMSO-D6) δ: 1.09 (d, 3H, J =
1H-NMR (DMSO-D6) δ: 1.08 (d, 3H, J =
1H-NMR (CDCl3) δ: 1.34 (d, 3H, J= 6.9
1H-NMR (CDCl3) δ: 1.36 (d, 3H, J= 6.9
1H-NMR (DMSO-D6) δ: 1.09 (d, 3H, J =
1H-NMR (DMSO-D6) δ: 1.09 (d, 3H, J =
1H-NMR (CDCl3) δ: 1.35 (d, 3H, J= 7.2
1H-NMR (DMSO-D6) δ: 1.08 (d, 3H, J =
1H-NMR (DMSO-D6) δ: 1.09 (d, 3H, J =
1H-NMR (DMSO-D6) δ: 1.09 (d, 3H, J =
1H-NMR (DMSO-D6) δ: 1.09 (d, 3H, J =
1H-NMR (CDCl3) δ: 1.34 (d, 3H, J= 6.9
1H-NMR (DMSO-D6) δ: 1.08 (d, 3H, J =
1H-NMR (DMSO-D6) δ: 1.08 (d, 3H, J =
1H-NMR (DMSO-D6) δ: 1.08 (d, 3H, J =
Compounds A to H, each of which is shown in the following table, were obtained according to the description of WO 2013/031922.
Metabolites 1, 3, and 5 (i.e., metabolites of Compounds of Examples 1, 3, and 5, respectively) and Metabolites C to H (i.e., metabolites of Compounds C to H, respectively), each of which is shown in the following table, were obtained according to the above Examples and the description of WO 2013/031922.
SGLT1 inhibitory activities of test compounds (IC50 values) were calculated based on the amount of intracellular uptake of labelled α-methyl-D-glucopyranoside (14C-AMG) transported by SGLT1.
A DNA fragment containing human SGLT1 was amplified by PCR (Polymerase Chain Reaction) using pCMV6-hSGLT1 (OriGene) as a template. In the human SGLT1, NheI recognition and cleavage sequence was added to the upstream of Kozac consensus sequence derived from a vector, and a stop codon, TAG, and SalI recognition and cleavage sequence were added to the immediate downstream of the protein-translating region of human SGLT1. The purified DNA fragment was cleaved by restriction enzymes NheI and SalI, followed by ligation with pcDNA3.1 (+) which was cleaved by NheI and XhoI, thereby forming human SGLT1-expressing plasmid. The nucleic acid sequence of human SGLT1 inserted into a vector was completely identical to the protein-translated region of human SGLT1 sequence (Accession number NM_000343) registered in GenBank, and the sequence of the portion connected to the vector was as expected.
Human SGLT-expressing plasmid, pcDNA-hSGLT1, was transfected into each CHO-K1 cell by Lipofectamine 2000 (Invitrogen) and cultured in the presence of G418 (Nacalai Tesque) to select drug-resistant cell lines. A cell line having the highest ratio (S/B ratio) of the amount of intracellular uptake of 14C-AMG per cell to the amount of intracellular uptake of 14C-AMG after treatment with a SGLT inhibitor, phlorizin, was selected as a human SGLT1-stably-expressing cell line from the drug-resistant cell lines.
Human SGLT1-stably-expressing cell lines were seeded at 5×104 cells/well on BioCoat™ Poly-D-Lysine 96 well plate with Lid (Becton, Dickinson and Company) and cultured at 37° C. under 5% CO2 overnight. The medium was replaced with 100 μL/well of Na(−) buffer (140 mM choline chloride, 2 mM KCl, 1 mM MgCl2, 1 mM CaCl2), 10 mM HEPES, 5 mM Tris, pH 7.4), and then the mixture was let stand at 37° C. under 5% CO2 for 20 minutes. After removal of Na(−) buffer, thereto was added 40 μL/well of a test compound solution prepared with Na(+) buffer (140 mM NaCl, 2 mM KCl, 1 mM MgCl2, 1 mM CaCl2, 10 mM HEPES, 5 mM Tris, pH 7.4) comprising BSA. Then, thereto was added 40 μL/well of Na(+) buffer comprising 8 kBq of 14C-AMG and 2 mM AMG, and the mixture was mixed well. For a blank, 40 μL/well of Na(−) buffer comprising BSA was added, and in addition, 40 μL/well of Na(−) buffer comprising 8 kBq of 14C-AMG and 2 mM AMG was added, and the mixture was mixed well. After incubation by being let stand for 1 hour at 37° C. under 5% CO2, cells were washed twice with 100 μL/well of ice-cooled wash buffer (100 mM AMG, 140 mM choline chloride, 2 mM KCl, 1 mM MgCl2, 1 mM CaCl2), 10 mM HEPES, 5 mM Tris, pH 7.4) to terminate the reaction. A cell lysate was prepared by addition of 50 μL/well of 0.2N aqueous NaOH solution. In the assessment for the uptake ability of 14C-AMG, the total amount of the cell lysate was transferred to OptiPlate 96 (Perkin-Elmer) with 100 μL/well of MicroScint-40 (Perkin-Elmer) dispensed and 14C of CPM was measured with TOPCOUNT NXT (Perkin-Elmer).
Data was calculated by deducting the average value of CPM for blank well from the average value of CPM for each well treated. An inhibition rate for each test compound in each concentration was calculated from the following equation:
[(A−B)/A]×100
wherein A is data for a solvent control and B is data for treatment with each test compound.
Each IC50 value (50% inhibitory concentration) for each test compound was calculated based on two concentrations before and after a 50% inhibition rate and the inhibition rate. Compound 1 was confirmed to have the SGLT1 inhibitory activity in the assessment. The test was carried out for other example compounds as well. Results are shown in the following table.
Vehicle (0.5% methylcellulose solution) or Compound 1 (1, 3, or 10 mg/kg) suspended in a 0.5% methylcellulose solution was orally administered in 5 mL/kg to an about 4-hour-fasted male SD rat (8-week old, Nihon Charles River K.K., 6 cases for each group). After 16 hours, glucose was loaded by oral administration of a 0.4 g/mL glucose solution in 5 mL/kg. Blood was collected from a tail vein just before the glucose load, and 30, 60 and 120 minutes after the glucose load; and the blood glucose level was measured with a biochemical automatic analyzer (HITACHI, Model No. 7180).
The results are shown in
Vehicle (0.5% methylcellulose solution), or Compound 1, Compound A, or Compound B (3 mg/kg each) suspended in a 0.5% methylcellulose solution was orally administered in 5 mL/kg to an about 4-hour-fasted male SD rat (8-week old, Nihon Charles River K.K., 5 cases for each group). After 16 hours, glucose was loaded by oral administration of a 0.4 g/mL glucose solution in 5 mL/kg. Blood was collected from a tail vein just before the glucose load, and 30, 60 and 120 minutes after the glucose load; and the blood glucose level was measured with a biochemical automatic analyzer (HITACHI, Model No. 7180).
The results are shown in
Metabolites 1, 3, and 5 and Metabolites C to H were each tested herein. The purpose of this test is to evaluate the potential of each metabolite to induce reverse mutations in the standard strains of Salmonella typhimurium (TA98, TA1537, TA100, and TA1535) and Escherichia coli (WP2uvrA), in either the presence or absence of a rat liver metabolic activation system (S9 mix).
The solvent used herein was dimethyl sulfoxide (DMSO, 100 μL/plate).
The test was performed by the pre-incubation method with or without S9 mix. When the test was performed without S9 mix, sodium phosphate buffer solution (pH 7.4) was added.
0.5 mL of S9 mix or 0.5 mL of 0.1 mol/L sodium phosphate buffer solution (pH 7.4), and 0.1 mL of the bacterial culture solution were added to a test tube containing 0.1 mL of the negative control formulation (DMSO alone), the metabolite, or the positive control formulation. The mixtures were pre-incubated at 37° C. for 20 minutes while shaking. After the pre-incubation period, 2 mL of top agar were added and the mixtures were vortex-mixed and seeded onto plates. Two plates per treatment were used. Each plate was incubated at 37±1° C. for 48 hours or more and the revertant colonies were counted. The mean number of revertant colonies for each treatment plate was then calculated. The presence or absence of growth inhibition due to any antibacterial effects of the test compounds and precipitation of the test compounds was observed grossly or under a stereomicroscope. The results were judged as positive if the mean number of revertant colonies showed a dose dependent increase which reached 2-fold over that of the negative control at one or more doses. Evaluation was based on mean values with no statistical comparisons being used.
The results of this test are shown in the following tables. In conclusion, Metabolites 1, 3, and 5 did not show potential to induce reverse mutations in any of the bacterial tester strains, whereas Metabolites C to H showed potential to induce reverse mutations in at least one of the bacterial tester strains with and/or without S9 mix. Details are explained as follows.
Metabolite C showed potential to induce reverse mutations in the bacterial tester strains of TA98 with S9 mix and TA100 with S9 mix.
Metabolite D showed potential to induce reverse mutations in the bacterial tester strains of TA98 and TA1537 with S9 mix.
Metabolite E showed potential to induce reverse mutations in the bacterial tester strains of TA98, TA1537, TA100, and TA1535 with S9 mix and TA1537 without S9 mix.
Metabolite F showed potential to induce reverse mutations in the bacterial tester strains of TA98, TA1537, and TA100 with S9 mix and WP2uvrA without S9 mix.
Metabolite G showed potential to induce reverse mutations in the bacterial tester strains of TA100 with S9 mix and TA1535 without S9 mix.
Metabolite H showed potential to induce reverse mutations in the bacterial tester strains of TA98, TA1537, and TA100 with S9 mix.
Effects of Combination Use with an SGLT2 Inhibitor in OGTT (Oral Glucose Tolerance Test)
Overnight-fasted male Zucker Fatty rats (7-week old, Nihon Charles River K.K.) were divided into groups on the basis of blood glucose levels and body weights (8 cases for each group). After the grouping, vehicle (0.5% methylcellulose solution), only Compound 1 (1 mg/kg), only dapagliflozin (3 mg/kg), or a combination of Compound 1 and dapagliflozin was orally administered in 5 mL/kg to the rats. After 4 hours, glucose was loaded by oral administration of a 0.4 g/mL glucose solution in 5 mL/kg. Blood was collected from a tail vein just before the glucose load, and 30, 60, 120, and 240 minutes after the glucose load; and blood glucose levels were measured with a biochemical automatic analyzer (HITACHI, Model No. 7180).
The results were shown by transition of blood glucose levels, the blood glucose levels 30 minutes after the glucose load, and the blood glucose levels 60 minutes after the glucose load. Statistical analyses were based on Tukey-kramer's multiple test. The significance level was two-sided 5%. The results showed that combination use of Compound 1 and dapagliflozin significantly reduced the blood glucose level compared to each of these drugs. The results are shown in
Effects of Combination Use with a DPP4 Inhibitor in OGTT (Oral Glucose Tolerance Test)
Overnight-fasted male Zucker Fatty rats (8-week old, Nihon Charles River K.K.) were divided into groups on the basis of blood glucose levels and body weights (8 cases for each group). After the grouping, vehicle (0.5% methylcellulose solution), only Compound 1 (1 mg/kg, 4 hours before the glucose load), only sitagliptin (3 mg/kg, 30 minutes before the glucose load), or a combination of Compound 1 and sitagliptin was orally administered in 5 mL/kg to the rats. Then, glucose was loaded by oral administration of a 0.4 g/mL glucose solution in 5 mL/kg. Blood was collected from a tail vein just before the glucose load, and 30, 60, and 120 minutes after the glucose load. Blood glucose levels were measured with a biochemical automatic analyzer (HITACHI, Model No. 7180). Active GLP-1 was measured with a GLP-1 assay kit (IBL, #27700).
The results of blood glucose levels were shown by their transition and the blood glucose levels after 30 minutes from the glucose load. The results of active GLP-1 were shown by its transition and concentration AUC. Statistical analyses for the blood glucose levels after 30 minutes from the glucose load and the concentration AUC of active GLP-1 were carried out based on Steel Dwass's multiple test. The significance level was two-sided 5%. The results show that combination use of Compound 1 and sitagliptin significantly reduced the blood glucose level compared to each of these drugs (
Formulation Examples of a compound of Formula [I] include, for example, the following formulations, but are not intended to be limited thereto.
Ingredients (1), (2), (3), and (4) are mixed to be filled in a gelatin capsule.
The total amount of Ingredients (1), (2), and (3) and 30 g of Ingredient (4) are combined with water, dried in vacuo, and then granulated. The resulted granules are mixed with 14 g of Ingredient (4) and 1 g of Ingredient (5), and tableted with a tableting machine. In this manner, 1000 tablets comprising 10 mg of Compound 1 for each tablet are obtained.
Use of an SGLT1 inhibitor in combination with at least one drug selected from SGLT2 inhibitors and DPP4 inhibitors is expected to be useful for treating and/or preventing various diseases or conditions that are expected to be alleviated by adjustment of the activities of these drugs or that may be caused by elevated blood glucose levels due to sugar absorption in the body.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2019-161526 | Sep 2019 | JP | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/JP2020/033463 | 9/3/2020 | WO |
