US20170066741A1 - 2-Amino-3,5,5-Trifluoro-3,4,5,6-Tetrahydropyridines as BACE1 Inhibitors for Treatment of Alzheimer's Disease - Google Patents

2-Amino-3,5,5-Trifluoro-3,4,5,6-Tetrahydropyridines as BACE1 Inhibitors for Treatment of Alzheimer's Disease Download PDF

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US20170066741A1
US20170066741A1 US15/119,639 US201515119639A US2017066741A1 US 20170066741 A1 US20170066741 A1 US 20170066741A1 US 201515119639 A US201515119639 A US 201515119639A US 2017066741 A1 US2017066741 A1 US 2017066741A1
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trifluoro
amino
fluorophenyl
dimethyl
tetrahydropyridin
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Karsten Juhl
Mauro Marigo
Lena Tagmose
Thomas Jensen
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H Lundbeck AS
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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/444—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring heteroatom, e.g. amrinone
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
    • C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D211/68—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member
    • C07D211/72—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, directly attached to ring carbon atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D227/00—Heterocyclic compounds containing rings having one nitrogen atom as the only ring hetero atom, according to more than one of groups C07D203/00 - C07D225/00
    • C07D227/02—Heterocyclic compounds containing rings having one nitrogen atom as the only ring hetero atom, according to more than one of groups C07D203/00 - C07D225/00 with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D227/06—Heterocyclic compounds containing rings having one nitrogen atom as the only ring hetero atom, according to more than one of groups C07D203/00 - C07D225/00 with only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D227/10—Nitrogen atoms not forming part of a nitro radical
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
    • C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links

Definitions

  • the present invention provides compounds which act as BACE1 inhibitors. Separate aspects of the invention are directed to pharmaceutical compositions comprising said compounds and uses of the compounds to treat Alzheimer's disease.
  • Dementia is a clinical syndrome characterized by deficits in multiple areas of cognition that cannot be explained by normal aging, a noticeable decline in function, and an absence of delirium. In addition, neuropsychiatric symptoms and focal neurological findings are usually present. Dementia is further classified based on etiology Alzheimer's disease (AD) is the most common cause of dementia, followed by mixed AD and vascular dementia, vascular dementia, Lewy body dementia (DLB), and fronto-temporal dementia.
  • AD Alzheimer's disease
  • vascular dementia vascular dementia
  • LLB Lewy body dementia
  • fronto-temporal dementia fronto-temporal dementia
  • ⁇ -Amyloid deposits and neurofibrillary tangles are considered to be major pathologic characterizations associated with AD which is characterized by the loss of memory, cognition, reasoning, judgment, and orientation. Also affected, as the disease progresses, are motor, sensory and linguistic abilities until global impairment of multiple cognitive functions occurs.
  • ⁇ -Amyloid deposits are predominantly an aggregate of A ⁇ peptide, which in turn is a product of the proteolysis of amyloid precursor protein (APP) as part of the ⁇ -amyloidogenic pathway, A ⁇ peptide results from the cleavage of APP at the C-terminals by one or more ⁇ -secretases and at the N-terminus by ⁇ -secretase enzyme (BACE1) also known as aspartyl protease 2.
  • BACE1 activity is correlated directly to the generation of A ⁇ peptide from APP.
  • BACE1 impedes the production of A ⁇ peptide.
  • BACE1 co-localizes with its substrate APP in Golgi and endocytic compartments (Willem M, et al. Semin. Cell Dev. Biol, 2009, 20, 175-182).
  • Knock-out studies in mice have demonstrated the absence of amyloid peptide formation while the animals are healthy and fertile (Ohno M, et al. Neurobiol. Dis., 2007, 26, 134-145).
  • Genetic ablation of BACE1 in APP-overexpressing mice has demonstrated absence of plaque formation, and the reversal of cognitive deficits (Ohno M, et al. Neuron; 2004, 41, 27-33).
  • BACE1 levels are elevated in the brains of sporadic AD patients (Hampel and Shen, Scand. J. Clin. Lab. Invest. 2009, 69, 8-12).
  • AstraZeneca announced the discovery of AZD3839, a potent and selected BACE1 inhibitor clinical candidate for the treatment of AD (Jeppsson, F., et al. JBC, 2012, 287, 41245-41257) in October 2012.
  • the effort which led to the discovery of AZD3839 was further described in Ginman, T., et al. Journal of Medicinal Chemistry, 2013, 56, 4181-4205.
  • the Ginman publication describes the issues which were overcome in connection with the discovery and identification of AZD3839. These issues related to poor blood brain barrier penetration and P-glycoprotein mediated efflux of the compounds resulting in lack of brain exposure.
  • the present invention relates to novel compounds having BACE1 inhibitory activity, to their preparation, to their medical use and to medicaments comprising them.
  • An objective of the present invention is to provide compounds that inhibit BACE1. Accordingly, the present invention relates to compounds of Formula I.
  • Ar is selected from the group consisting of phenyl, pyridyl, pyrimidyl, pyrazinyl, imidazolyl, pyrazolyl, 1,2,4-triazolyl, thiophenyl, thiazolyl, oxazolyl, isoxazolyl, 1,3,4-thiadiazolyl, isothiazolyl, 1,3,4-oxadiazolyl, 1,2,4-oxadiazolyl, furazanyl and 1,2,4-thiadiazolyl and where the Ar is optionally substituted with one or more halogen, CN, C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 1 -C 6 fluoroalkyl or C 1 -C 6 alkoxy;
  • R 1 is C 1 -C 3 alkyl or C 1 -C 3 fluoroalkyl
  • R 2 is hydrogen, halogen, C 1 -C 3 fluoroalkyl or C 1 -C 3 alkyl
  • R 3 is C 1 -C 3 alkyl; or a pharmaceutically acceptable salt thereof.
  • the present invention further provides a pharmaceutical composition comprising a therapeutically effective amount of a compound of Formula I and a pharmaceutically acceptable carrier.
  • the present invention provides a method of treating a subject suffering from Alzheimer's disease comprising administering to the subject a therapeutically effective amount of a compound of Formula I.
  • the present invention is directed to the use of a compound as defined in Formula I for the manufacture of a medicament for treating Alzheimer's disease.
  • the compound is of formula Ia
  • R 1 is CH 3 .
  • R 2 is F or H.
  • R 3 is CH 3 .
  • Ar is optionally substituted with one or more F, Cl, CN, C 1 -C 3 alkyl, C 1 -C 3 fluoroalkyl or C 1 -C 3 alkoxy.
  • the stereochemistry is (2R,5S).
  • Ar is optionally substituted phenyl.
  • Ar is optionally substituted pyridyl.
  • Ar is optionally substituted pyrimidyl.
  • Ar is optionally substituted pyrazinyl.
  • Ar is optionally substituted imidazolyl.
  • Ar is optionally substituted pyrazolyl.
  • Ar is optionally substituted 1,2,4-triazolyl.
  • Ar is optionally substituted thiophenyl.
  • Ar is optionally substituted oxazolyl.
  • Ar is optionally substituted isoxazolyl.
  • Ar is optionally substituted 1,3,4-thiadiazolyl.
  • Ar is optionally substituted thiazolyl.
  • Ar is optionally substituted isothiazolyl.
  • Ar is optionally substituted 1,3,4-oxadiazolyl.
  • Ar is optionally substituted 1,2,4-oxadiazolyl.
  • Ar is optionally substituted furazanyl.
  • Ar is optionally substituted 1,2,4-thiadiazolyl.
  • the compound is selected from one of the exemplified compounds disclosed in the Experimental Section.
  • a separate embodiment is directed to a pharmaceutical composition
  • a pharmaceutical composition comprising the compound or a pharmaceutically acceptable salt thereof and a pharmaceutically acceptable carrier.
  • Another embodiment is directed to a method of treating Alzheimer's disease comprising administering a therapeutically effective amount of the compound.
  • Yet another embodiment is directed to a use of a compound for the manufacture of a medicament for treating Alzheimer's disease.
  • One embodiment is a compound for use in therapy.
  • Yet another embodiment is directed to a compound for use in the treatment of Alzheimer's disease.
  • isotopically labelled compounds which are identical to those claimed in formula I, where one or more atoms are replaced by an atom having an atomic mass or mass number different from the atomic mass or mass number usually found in nature.
  • isotopes that can be incorporated into compounds of the invention include isotopes of hydrogen, carbon, nitrogen, oxygen, sulfur, fluorine, chlorine and iodine, such as 2 H, 3 H, 13 C, 11 C, 14 C, 15 N, 18 O, 17 O, 35 S, 18 F, 36 Cl and 125 I, respectively.
  • FIG. 1 shows the two molecules in the asymmetric unit as found in the crystal structure.
  • the X-ray method used cannot distinguish between hydrogen ( 1 H) and deuterium (D or 2 H).
  • the deuterium atoms in the d3-methoxy group are depicted as hydrogen.
  • the present invention is based on the discovery that the compounds of Formula I are inhibitors of BACE1, and as such, are useful for the treatment of related disorders. Certain aspects of the invention are explained in greater detail below but this description is not intended to be a detailed catalog of all the different ways in which the invention may be implemented, or all the features that may be added to the present invention. Hence, the following specification is intended to illustrate some embodiments of the invention, and not to exhaustively specify all permutations, combinations and variations thereof.
  • C 1 -C 6 alkyl refers to a straight chained or branched saturated hydrocarbon having from one to six carbon atoms, inclusive.
  • substituents include, but are not limited to, methyl, ethyl, 1-propyl, 2-propyl, 1-butyl, 2-butyl, 2-methyl-2-propyl, 2-methyl-1-propyl, n-pentyl and n-hexyl.
  • straight chained or branched C 1 -C 3 alkyl refers to a saturated hydrocarbon having from one to three carbon atoms, inclusive. Examples of such substituents include, but are not limited to, methyl, ethyl and n-propyl.
  • C 1 -C 6 alkoxy refers to a straight chained or branched saturated alkoxy group having from one to six carbon atoms, inclusive, with the open valency on the oxygen. Examples of such substituents include, but are not limited to, methoxy, ethoxy, n-butoxy, t-butoxy and n-hexyloxy.
  • the “C 1 -C 6 alkoxy” is optionally substituted with one or more fluorine atoms.
  • C 1 -C 6 fluoroalkyl refers to a straight chained or branched saturated hydrocarbon having from one to six carbon atoms inclusive substituted with one or more fluorine atoms.
  • substituents include, but are not limited to, trifluoromethyl, pentafluoroethyl, 1-fluoroethyl, monofluoromethyl, difluoromethyl, 1,2-difluoroethyl and 3,4 difluorohexyl.
  • straight chained or branched C 1 -C 3 fluoroalkyl refers to a saturated hydrocarbon having from one to three carbon atoms, inclusive, substituted with one or more fluorine atoms per carbon atom.
  • halogen refers to fluorine, chlorine, bromine and iodine.
  • C 2-6 -alkenyl refers to a branched or unbranched alkenyl group having from two to six carbon atoms and one double bond, including but not limited to ethenyl, propenyl, and butenyl.
  • C 2-6 -alkynyl shall mean a branched or unbranched alkynyl group having from two to six carbon atoms and one triple bond, including but not limited to ethynyl, propynyl and butynyl.
  • each compound number corresponds to the number of the experiment in which the method of manufacture is disclosed.
  • Compounds 4 and 18 have resynthesized using a modified method of manufacture as disclosed in examples 4a and 18a.
  • the phrase “effective amount” when applied to a compound of the invention is intended to denote an amount sufficient to cause an intended biological effect.
  • the phrase “therapeutically effective amount” when applied to a compound of the invention is intended to denote an amount of the compound that is sufficient to ameliorate, palliate, stabilize, reverse, slow or delay the progression of a disorder or disease state, or of a symptom of the disorder or disease.
  • the method of the present invention provides for administration of combinations of compounds. In such instances, the “effective amount” is the amount of the combination sufficient to cause the intended biological effect.
  • treatment means ameliorating or reversing the progress or severity of a disease or disorder, or ameliorating or reversing one or more symptoms or side effects of such disease or disorder.
  • Treatment or “treating”, as used herein, also means to inhibit or block, as in retard, arrest, restrain, impede or obstruct, the progress of a system, condition or state of a disease or disorder.
  • treatment or “treating” further means an approach for obtaining beneficial or desired clinical results, where “beneficial or desired clinical results” include, without limitation, alleviation of a symptom, diminishment of the extent of a disorder or disease, stabilized (i.e., not worsening) disease or disorder state, delay or slowing of a disease or disorder state, amelioration or palliation of a disease or disorder state, and remission of a disease or disorder, whether partial or total, detectable or undetectable.
  • the present invention also provides a method of treating a disease or disorder, the method comprises administering a therapeutically effective amount of at least one compound of the present invention or a pharmaceutically acceptable salt thereof to a mammal in need thereof, wherein the disease or disorder is a neurodegenerative or cognitive disease or disorder.
  • the neurodegenerative or cognitive disease or disorder is Alzheimer's disease, mild cognitive impairment, Trisomy 21 (Down Syndrome), cerebral amyloid angiopathy, Hereditary Cerebral Hemorrhage with Amyloidosis of the Dutch-Type (HCHWA-DT), degenerative dementia, amyotrophic lateral sclerosis, traumatic brain injury or stroke.
  • the disease or disorder is a peripheral amyloidosis, such as amyloid neuropathy or pancreatitis.
  • the disease or disorder is peripheral nerve damage.
  • the present invention provides a method of treating Alzheimer's disease in a patient comprising administering to a patient in need of such treatment a therapeutically effective amount of at least one compound of formula I.
  • the present invention further provides a method of inhibiting BACE1 in a patient comprising administering to a patient in need thereof a therapeutically effective amount of at least one compound of formula I.
  • the present invention also provides a method of inhibiting ⁇ -secretase mediated cleavage of amyloid precursor protein comprising administering to a patient in need of such treatment a therapeutically effective amount of at least one compound of formula I.
  • the present invention provides the use of a compound of formula I for the manufacture of a medicament for the treatment of Alzheimer's disease.
  • the present invention also provides the use of a compound of formula I for the manufacture of a medicament for the inhibition of BACE1.
  • the present invention further provides the use of a compound of formula I for the manufacture of a medicament for the inhibition of production or accumulation of A ⁇ peptide.
  • the invention also provides a compound of formula I for use in therapy of a patient, for example, in the treatment of Alzheimer's disease or to slow the progression of a patient's mild cognitive impairment to Alzheimer's disease.
  • the invention provides a pharmaceutical formulation adapted for any of the above treatments and uses.
  • the mammal of the method of the invention is a human.
  • the patient of the method of the invention is a human patient.
  • At least one symptom of the neurodegenerative or cognitive disease or disorder is treated.
  • the present invention also comprises salts of the present compounds, typically, pharmaceutically acceptable salts.
  • Such salts include pharmaceutically acceptable acid addition salts.
  • Acid addition salts include salts of inorganic acids as well as organic acids.
  • suitable inorganic acids include hydrochloric, hydrobromic, hydroiodic, phosphoric, sulfuric, sulfamic, nitric acids and the like.
  • suitable organic acids include formic, acetic, trichloroacetic, trifluoroacetic, propionic, benzoic, cinnamic, citric, fumaric, glycolic, itaconic, lactic, methanesulfonic, maleic, malic, malonic, mandelic, oxalic, picric, pyruvic, salicylic, succinic, methane sulfonic, ethanesulfonic, tartaric, ascorbic, pamoic, bismethylene salicylic, ethanedisulfonic, gluconic, citraconic, aspartic, stearic, palmitic, EDTA, glycolic, p-aminobenzoic, glutamic, benzenesulfonic, p-tol
  • the compounds of this invention may exist in unsolvated as well as in solvated forms with pharmaceutically acceptable solvents such as water, ethanol and the like.
  • the compounds of the present invention may have one or more asymmetric centres and it is intended that any optical isomers (i.e. enantiomers or diastereomers), as separated, pure or partially purified optical isomers, and any mixtures thereof including racemic mixtures, i.e. a mixture of stereoisomeres, are included within the scope of the invention.
  • any optical isomers i.e. enantiomers or diastereomers
  • pure or partially purified optical isomers i.e. a mixture of stereoisomeres
  • one embodiment of the invention relates to a compound of the invention having an enantiomeric excess of at least 60%, at least 70%, at least 80%, at least 85%, at least 90%, at least 96%, preferably at least 98%.
  • Racemic forms may be resolved into the optical antipodes by known methods, for example, by separation of diastereomeric salts thereof with an optically active acid, and liberating the optically active amine compound by treatment with a base. Separation of such diastereomeric salts can be achieved, e.g. by fractional crystallization.
  • the optically active acids suitable for this purpose may include, but are not limited to d- or l-tartaric, mandelic or camphorsulfonic acids. Another method for resolving racemates into the optical antipodes is based upon chromatography on an optically active matrix.
  • the compounds of the present invention may also be resolved by the formation and chromatographic separation of diastereomeric derivatives from chiral derivatizing reagents, such as, chiral alkylating or acylating reagents, followed by cleavage of the chiral auxiliary. Any of the above methods may be applied either to resolve the optical antipodes of the compounds of the invention per se or to resolve the optical antipodes of synthetic intermediates, which can then be converted by methods described herein into the optically resolved final products which are the compounds of the invention.
  • Optically active compounds can also be prepared from optically active starting materials.
  • the present invention further provides a pharmaceutical composition comprising a therapeutically effective amount of a compound of Formula I and a pharmaceutically acceptable carrier.
  • the present invention also provides a pharmaceutical composition comprising a therapeutically effective amount of one of the specific compounds disclosed in the description, such as in the experimental section and a pharmaceutically acceptable carrier.
  • the compounds of the invention may be administered alone or in combination with pharmaceutically acceptable carriers or excipients, in either single or multiple doses.
  • the pharmaceutical compositions according to the invention may be formulated with pharmaceutically acceptable carriers or diluents as well as any other known adjuvants and excipients in accordance with conventional techniques such as those disclosed in Remington: The Science and Practice of Pharmacy, 21 th Edition, Troy, Ed., Lippincott Williams &Wilkins, Baltimore, Md., USA.
  • compositions for oral administration include solid dosage forms such as capsules, tablets, dragees, pills, lozenges, powders and granules. Where appropriate, the compositions may be prepared with coatings such as enteric coatings or they may be formulated so as to provide controlled release of the active ingredient such as sustained or prolonged release according to methods well known in the art.
  • Liquid dosage forms for oral administration include solutions, emulsions, suspensions, syrups and elixirs.
  • Pharmaceutical compositions for parenteral administration include sterile aqueous and nonaqueous injectable solutions, dispersions, suspensions or emulsions as well as sterile powders to be reconstituted in sterile injectable solutions or dispersions prior to use.
  • Other suitable administration forms include, but are not limited to, suppositories, sprays, ointments, creams, gels, inhalants, dermal patches and implants.
  • Typical oral dosages range from about 0.01 to about 100 mg/kg body weight per day.
  • the compounds of this invention are generally utilized as the free substance or as a pharmaceutically acceptable salt thereof.
  • One example is an acid addition salt of a compound having the utility of a free base.
  • a compound of Formula I contains a free base such salts are prepared in a conventional manner by treating a solution or suspension of a free base of Formula I with a molar equivalent of a pharmaceutically acceptable acid.
  • suitable organic and inorganic acids are described above.
  • Suitable pharmaceutical carriers include inert solid diluents or fillers, sterile aqueous solutions and various organic solvents.
  • solid carriers include lactose, terra alba, sucrose, cyclodextrin, talc, gelatin, agar, pectin, acacia, magnesium stearate, stearic acid and lower alkyl ethers of cellulose.
  • liquid carriers include, but are not limited to, syrup, peanut oil, olive oil, phospholipids, fatty acids, fatty acid amines, polyoxyethylene and water.
  • the carrier or diluent may include any sustained release material known in the art, such as glyceryl monostearate or glyceryl distearate, alone or mixed with a wax.
  • sustained release material such as glyceryl monostearate or glyceryl distearate, alone or mixed with a wax.
  • the preparation may be tabletted, placed in a hard gelatin capsule in powder or pellet form or it may be in the form of a troche or lozenge.
  • the amount of solid carrier will vary widely but will range from about 25 mg to about 1 g per dosage unit.
  • the preparation may be in the form of a syrup, emulsion, soft gelatin capsule or sterile injectable liquid such as an aqueous or non-aqueous liquid suspension or solution.
  • Schemes 1-2 describe the use of selective protecting groups during the synthesis of the compounds of the invention.
  • One skilled in the art would be able to select the appropriate protecting group for a particular reaction.
  • Methods for protection and deprotection of such groups are well known in the art, and may be found in T. Green, et al., Protective Groups in Organic Synthesis, 1991, 2 nd Edition, John Wiley & Sons, New York.
  • LC-MS were run on Waters Acquity UPLC-MS consisting of Waters Acquity including column manager, binary solvent manager, sample organizer, PDA detector (operating at 254 nm), ELS detector, and TQ-MS equipped with APPI-source operating in positive ion mode.
  • LC-conditions The column was Acquity UPLC BEH C18 1.7 ⁇ m; 2.1 ⁇ 50 mm operating at 60° C. with 1.2 ml/min of a binary gradient consisting of water+0.05% trifluoroacetic acid (A) and acetonitrile+5% water+0.05% trifluoroacetic acid. Gradient: 0.00 min: 10% B; 1.00 min: 100% B; 1.01 min: 10% B; 1.15 min: 10% B. Total run time: 1.15 min.
  • LC-MS were run on Waters Aquity UPLC-MS consisting of Waters Aquity including column manager, binary solvent manager, sample organizer, PDA detector (operating at 254 nM), ELS detector, and SQ-MS equipped with APPI-source operating in positive ion mode.
  • LC-conditions The column was Acquity UPLC BEH C18 1.7 ⁇ m; 2.1 ⁇ 150 mm operating at 60° C. with 0.6 ml/min of a binary gradient consisting of water+0.05% trifluoroacetic acid (A) and acetonitrile+5% water+0.03% trifluoroacetic acid. Gradient: 0.00 min: 10% B; 3.00 min: 99.9% B; 3.01 min: 10% B; 3.60 min: 10% B. Total run time: 3.60 min.
  • R 1 and R 3 are as defined under formula I
  • R 4 and R 5 are an alkyl group such as methyl or ethyl
  • R 6 and R 7 are independently selected amine protection groups such as a tert-butoxy carbonyl group.
  • Compounds of the general formula IV may be prepared by reacting compounds of the general formula II with a sulfinamide such as III in the presence of a Lewis acid/drying agent such as titanium tetraethoxide.
  • a Lewis acid/drying agent such as titanium tetraethoxide.
  • Treatment of compounds of the general formula IV with compounds of the general formula V such as ethyl bromodifluoroacetate in the presence of Zn powder or in the presence of diethyl zinc and tris(triphenylphosphine)rhodium(I) chloride gives compounds of the general formula VI.
  • Compounds of the general formula VII are obtained from compounds of the general formula VI by treatment with a reducing agent such as diisobutylaluminium hydride.
  • compound VII might be in the hydrate form or an oligomeric form thereof.
  • Treatment of compounds of the general formula VII with conditions such as ethyl 2-(diethoxyphosphoryl)-2-fluoroacetate in the presence of lithium chloride and a base such as N,N-diisopropylethylamine gives compounds of the general formula VIII.
  • Compounds of the general formula IX are obtained by hydrogenation of compounds of the general formula VIII in the presence of a catalyst such as palladium on carbon.
  • Compounds of the general formula X are obtained by treatment of compounds of the general formula IX with an acid such as hydrochloric acid in methanol followed by treatment with potassium carbonate in methanol.
  • R 1 , R 2 , R 3 and Ar are as defined under formula I and R 7 is an amine protection groups such as a tert-butoxy carbonyl group.
  • R 1 , R 2 , R 3 and Ar are as defined under formula I.
  • Compounds of the general formula XXI (Scheme 3) can be obtained by treatment of compounds of the general formula XVII with ammonia.
  • Compounds of the general formula I may be prepared by reacting compounds of the general formula XXI with a carboxylic acid chloride of general formula XVIII or by reaction with a carboxylic acid of general formula XIX using procedures known to chemists skilled in the art.
  • Tris(triphenylphosphine)rhodium(I) chloride (1.50 g, 1.62 mmol) was placed in a dry round bottom flask. The flask was evacuated and filled with argon ( ⁇ 3).
  • (R)—N-(1-(2-Fluorophenyl)ethylidene)-2-methylpropane-2-sulfinamide (15.6 g, 64.6 mmol) was dissolved in tetrahydrofuran (265 ml) (dried over 4 ⁇ MS) and added to the reaction flask followed by ethyl bromodifluoroacetate (26.2 g, 16.6 ml, 129 mmol).
  • the dark red/orange reaction mixture was cooled to 0° C. using an ice/water bath. Diethyl zinc (126 ml, 126 mmol, 1 M in hexane) was added in a dropwise manner. Upon complete addition the reaction was stirred at 0° C. for an additional 1 h, the cooling was removed and the reaction was stirred at room temperature overnight. The reaction was diluted with ethyl acetate (250 mL) and quenched with saturated aqueous NaHCO 3 (100 mL). The resulting suspension was filtered through a plug of celite, the phases were separated, and the organic layer was dried over MgSO 4 , filtered, and concentrated under reduced pressure.
  • DIBAL-H (41.6 ml, 41.6 mmol, 1 M in toluene) was added in a dropwise manner using a syringe pump (addition rate 1 mL/min) Upon complete addition the reaction was stirred at ⁇ 78° C. for an additional 1 h 20 min. The reaction was quenched at ⁇ 78° C. by addition of 10 mL of ethyl acetate followed by addition of 150 mL of a saturated aqueous solution of sodium potassium tartrate. Upon complete addition the cooling was removed, the reaction allowed to warm to room temperature and stirred at this temperature for 1 h.
  • the mixture was diluted with ethyl acetate (200 mL) and filtered through a plug of celite using ethyl acetate for elution. The filtrate was transferred to a separation funnel and the organic layer was isolated. The aqueous phase was extracted with ethyl acetate (2 ⁇ 100 mL), the combined organics were washed with brine (100 mL), dried over MgSO 4 , filtered, and concentrated under reduced pressure to afford an intermediate. The intermediate was used immediately in the subsequent step without further purification. Lithium chloride (2.20 g, 52.0 mmol) was placed in a round bottom flask, dried under vacuum with heating and allowed to cool to room temperature under vacuum.
  • Acetonitrile (87 mL) was added followed by ethyl 2-(diethoxyphosphoryl)-2-fluoroacetate (5.79 g, 23.9 mmol).
  • the solution was cooled to 0° C. using an ice/water bath and N,N-diisopropylethylamine (4.03 g, 5.5 ml, 31.2 mmol) was added. After 10 min stirring at this temperature a solution of the intermediate mentioned above in acetonitrile (33 ml) was added. Upon complete addition the cooling was removed and the reaction was stirred overnight at room temperature.
  • the reaction mixture was concentrated to approximately 50 mL (under vacuum), ethyl acetate (250 mL), water (50 mL) and saturated aqueous NH 4 Cl (50 mL) were added. The phases were separated and the aqueous layer was extracted with ethyl acetate (2 ⁇ 100 mL). The combined organics were dried over MgSO 4 , filtered, and concentrated under reduced pressure.
  • LiHMDS lithium hexamethyldisilazide
  • Methyl iodide (2.55 g, 1.13 mL, 18 mmol) was added in a dropwise manner and the solution was stirred at ⁇ 78° C. for 45 min then the cooling was removed and the solution was stirred for another 15 min at room temperature.
  • the solution was re-cooled to ⁇ 78° C. and quenched with saturated aqueous NH 4 Cl (25 mL). The cooling bath was removed and the reaction was allowed to warm to room temperature.
  • the reaction was diluted with toluene (50 mL) and concentrated to approximately 25 mL under vacuum. The residue was diluted with ethyl acetate (150 mL) and washed with saturated aqueous NaHCO 3 (50 mL). The phases were separated and the aqueous layer was extracted with ethyl acetate (2 ⁇ 75 mL). The combined organics were washed with brine, dried over MgSO 4 , filtered, and concentrated under reduced pressure.
  • the reaction was carefully evacuated and backfilled with argon ( ⁇ 3).
  • the suspension was heated to 80° C.
  • the reaction was stirred at this temperature for 3 h 30 min.
  • the reaction was allowed to cool to room temperature and concentrated under reduced pressure.
  • the crude material was suspended in CHCl 3 and filtered.
  • tert-butyl (4-fluoro-3-((2R,5S)-3,3,5-trifluoro-2,5-dimethyl-6-thioxopiperidin-2-yl)phenyl)carbamate (1.15 g, 2.83 mmol) was dissolved in dichloromethane (13 ml). The solution was cooled to 0° C. and TFA (6.5 ml, 84 mmol) was added. The solution was stirred at 0° C. for 1 h 20 min. The reaction was diluted with toluene (25 mL) and concentrated to approx 10 mL under reduced pressure.
  • tert-butyl (4-fluoro-3-((2R,5R)-3,3,5-trifluoro-2,5-dimethyl-6-thioxopiperidin-2-yl)phenyl)carbamate 816 mg, 2.01 mmol was dissolved in dichloromethane (9.2 mL). The solution was cooled to 0° C. and TFA (4.6 mL, 59.5 mmol) was added. The solution was stirred at 0° C. for 1 h 20 min. The reaction was diluted with toluene (15 mL) and concentrated to approx. 10 mL under reduced pressure.
  • Methyl 5-hydroxypicolinate (2.88 g, 18.81 mmol) was dissolved in DMF (108 mL). Potassium carbonate (7.20 g, 52.1 mmol) was added and the suspension was stirred for 45 minutes at room temperature. Methyl-d 3 -iodide (3.27 g, 1.40 ml, 22.6 mmol) was added. The reaction mixture was stirred at room temperature for 2 hours.
  • 5-fluoropicolinic acid (269 mg, 1.906 mmol) and 1-[bis(dimethylamino)methylene]-1H-1,2,3-triazolo-[4,5-b]pyridinium 3-oxid hexafluorophosphate (HATU) (797 mg, 2.10 mmol) were placed in a round bottom flask, dissolved in DMF (5.2 mL), and stirred at room temperature for 5 min.
  • HATU 1-[bis(dimethylamino)methylene]-1H-1,2,3-triazolo-[4,5-b]pyridinium 3-oxid hexafluorophosphate
  • the crude material was purified using a RediSep Automated flash system on 80 g silica gel (eluent: ethyl acetate/heptane).
  • the product was further purified by the following procedure: The product was dissolved in ethyl acetate (50 mL) and washed with a solution of saturated aqueous NaHCO 3 /water (1/1). The organic phase was washed total of 15 times (using 10 mL each time).
  • Crystals were obtained by recrystallization of compound 48 from a mixture of heptane and ethyl acetate.
  • the structure of compound 48 was elucidated by X-ray crystallography of said crystals.
  • the two molecules in the asymmetric unit as found in the X-ray structure of compound 48 are shown in FIG. 1 and shows that the stereoconfiguration is (2R,5S).
  • the binding assay was performed as SPA-based assay using a biotinylated form of human BACE1 recombinantly expressed and subsequently purified from Freestyle HEK293 cells.
  • the binding assay was run in a 50 mM sodium acetate buffer, pH 4.5 containing 50 mM NaCl and 0.03% Tween-20 in white clear bottom 384 plates (Corning #3653).
  • radioligand [ 3 H]—N-((1 S,2R)-1-benzyl-3-cyclopropylamino-2-hydroxy-propyl)-5-(methanesulfonyl-methyl-amino)-N—((R)-1-phenyl-ethyl)-isophthalamide
  • TRQ11569 purchased from GE Healthcare
  • test compound was mixed with test compound at a given concentration, 6 nM (final concentration) human BACE1 and 25 ⁇ g Streptavidin coated PVT core SPA beads (RPNQ0007, GE Healthcare Life Sciences) in a total volume of 40 ⁇ l.
  • Several concentrations of each test compound were tested in the assay for IC 50 determination.
  • IC 50 value the concentration mediating 50% inhibition of the specific binding of the radioligand
  • the K d of the radioligand was determined from saturation binding experiments.
  • the efficacy assay was performed as a FRET-based assay using a commercially available BACE1 kit (Life Technologies, P2985). 2 ⁇ l test compound at 10 ⁇ M (final concentration) and 15 ⁇ l BACE1 enzyme from the kit (final concentration 3 nM) were preincubated for 15 minutes at room temperature before addition of 15 ml of substrate from the kit (250 nM final concentration) and incubated for additional 90 minutes at room temperature. The assay plate was subsequently read in a Pherastar (Ex540/Em590).
  • the enzyme activity observed in presence of test compound were normalized to the enzyme activity observed in presence of buffer and 10 ⁇ M (final concentration) of the high affinity BACE1 reference inhibitor (S)-6-[3-Chloro-5-(5-prop-1-ynyl-pyridin-3-yl)-thiophen-2-yl]-2-imino-3,6-dimethyl-tetra-hydropyrimidin-4-one, respectively.
  • S high affinity BACE1 reference inhibitor
  • S high affinity BACE1 reference inhibitor
  • the animals undergoing treatment were closely monitored by veterinary staff for any signs of toxicity. Monitoring parameters included body weight, physical appearance, changes in coat appearance, occurrence of unprovoked behavior, and blunted or exaggerated responses to external stimuli.
  • Trunk-blood was sampled in EDTA coated tubes after decapitation of the animal.
  • the blood was centrifuged at 2200 G at 4° C. for 15 minutes and the plasma was collected and frozen at ⁇ 80° C.
  • the blood was aliquoted for A ⁇ ELISA and DMPK analysis Immediately following sacrifice, the brain was extracted and split into 2 halves. The right hemibrains were snap frozen on dry ice and stored at ⁇ 80° C. The left half was dissected; with the front forebrain taken for A ⁇ ELISA and the remainder used for DMPK analysis. These samples were also snap frozen on dry ice and stored at ⁇ 80° C. until use for analysis.
  • the cortex samples were thawed slightly on wet ice before they were homogenized with a small volume dispersing instrument (T10 basic ULTRA-TURRAX®) which was set at speed 5 for approximately 5-7 sec.
  • the tissue was processed in a 10 times volume of the weight, for example 100 mg of tissue was homogenized in 1000 ⁇ L of Homogenization buffer.
  • Homogenization buffer 50 ml Milli Q water+50 nM NaCl+0.2% Diethylamin (DEA)+1 tablet of Complete Protease inhibitor cocktail+1 nM 4-(2-aminoethyl) benzenesulfonyl fluoride hydrochloride irreversible serine protease inhibitor (AEBSF).
  • WAKO 294-62501 Human/Rat Abeta amyloid (40) kit was used for all ELISA analyses.
  • 30 ⁇ L plasma samples or 30 ⁇ L of the cortex supernatants generated as described above were placed in 600 ⁇ L microtubes tubes on wet ice.
  • 30 ⁇ L of 8M Urea AppliChem A1049, 9025
  • Both plasma and cortex supernatants are incubated on ice for 30 min.
  • Standard rows were prepared from the standard peptide stock provided in the kit and standard diluent containing 1.6M Urea (200 ⁇ L 8M Urea+800 ⁇ L of standard diluent) and 0.8M Urea (400 ⁇ L 8M Urea+3600 ⁇ L Standard diluent).
  • a serial 2-fold dilution of A ⁇ 40 from 100 pmol/ml to 0 pmol/L was prepared for the assay.
  • TMB 3,3′,5,5′-Tetramethylbenzidine
  • Concentration of A ⁇ in the samples was determined based on a standard curve generated from standards containing known concentrations of synthetic A ⁇ 40. Those skilled in the art will appreciate that diethylamine (DEA) and urea extractions will release soluble A ⁇ , and insoluble A ⁇ respectively. Since the ELISA kit is validated and widely used, it is accepted that as long as the treatment conditions and assay conditions are the same for each compound tested, then the assay should yield consistent robust data for the compounds tested and produce minimal discrepancies.
  • DEA diethylamine
  • the interpolated values of the samples loaded on plates are multiplied by 20 to account for the dilutions made when the volumes of DEA, urea and neutralization solution were added up. Values are calculated as percentage change in A ⁇ 40 compared to vehicle treated animals.
  • Compounds 1, 5, 17, 18, and 24 were administered at doses of 10 or 30 mg/kg p.o. and brain and plasma samples were collected at 3 hours post dose and the following exposures and reductions in A ⁇ 40 levels were measured as described above.
  • compounds of the present invention are able to penetrate the blood brain barrier and are efficacious in lowering A ⁇ 40 levels in the brain of animals.

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US10058540B2 (en) 2014-11-10 2018-08-28 H. Lundbeck A/S 2-amino-5,5-difluoro-6-(fluoromethyl)-6-phenyl-3,4,5,6-tetrahydropyridines as BACE1 inhibitors
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BR112018013247A2 (pt) 2016-10-28 2018-12-04 H Lundbeck As tratamentos de combinação compreendendo imidazopirazinonas para o tratamento de distúrbios psiquiátricos e/ou cognitivos
BR112018017058A2 (pt) 2016-12-21 2019-07-02 H Lundbeck As 6-amino-5-fluoro-5-(fluorometil)-2,3,4,5-tetra-hidropiridin-2-il-fenil-5-(metóxi-d3)-pirazina-2-carboxamidas e derivados fluorados do mesmo como inibidores de bace1
AU2018346712B2 (en) 2017-10-05 2021-04-01 Fulcrum Therapeutics, Inc. P38 kinase inhibitors reduce DUX4 and downstream gene expression for the treatment of FSHD
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PL3723807T3 (pl) 2017-12-14 2022-01-24 H. Lundbeck A/S Leczenie skojarzone obejmujące podawanie 1h-pirazolo­[4,3-b]pirydyn
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KR102507861B1 (ko) 2018-04-19 2023-03-09 삼성에스디에스 주식회사 부채널 공격에 안전한 연산 장치 및 방법
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