Patent Application
20230286988
The present invention relates to new pyrazolo[1,5-a]pyrimidine derivatives of formula (I) or pharmaceutically acceptable salts, biologically active metabolites, pro-drugs, racemates, enantiomers, diastereomers, solvates and hydrates thereof that serve as GABAB receptor positive allosteric modulators. The invention also relates to the process for producing such compounds as well as key intermediates of the process. The invention further relates to pharmaceutical compositions comprising such compounds optionally in combination with two or more different therapeutic agents and the use of such compounds in methods for treating diseases and conditions mediated and modulated by the GABAB receptor positive allosteric mechanism. The invention also provides a method for manufacture of medicaments useful in the treatment of such disorders.
Gamma-aminobutyric acid (GABA) is the main inhibitory neurotransmitter in the central nervous system and plays a key role in modulating neuronal activity. It exerts its action via three receptor systems, the related ionotropic GABAA and GABAC receptors, and the distinct metabotropic GABAB receptors (Hill and Bowery, Nature 1981, 290, 149-152). The latter GABAB receptors are widespreadly distributed within the mammalian central nervous system with various expression levels in different brain regions (Bovery et al, Neuroscience 1987, 20, 365-385). GABAB receptors can be found both pre- and postsynaptically and play an important role in the fine-tuning of neurotransmission. Most GABAB receptors cluster around excitatory synapses, either at the edge of the presynaptic terminal or on dendritic spines opposite to glutamatergic boutons (Ulrich and Bettler, Curr. Opin. Neurobiol. 2007, 17, 298-303).
GABAB receptors belong to the Family 3 (C) of G-protein coupled receptors (GPCRs) together with metabotropic glutamate receptors (mGluRs), calcium-sensing receptors, taste receptors and a number of orphan receptors, showing highest, approximately 30% homology to mGluRs (Bettler et al, Physiol. Rev. 2004, 84, 835-867). GABAB receptors are heterodimers consisting of two similar, yet different subunits, B1 and B2. The B1 subunit has multiple splice variants with only two (B1a and B1b) having clear physiological significance. These isoforms differ only in their extracellular domain containing two Sushi motifs that regulate the subcellular localization of the receptor (Vigot et al, Neuron 2006, 50, 589-601; Biermann et al, J. Neurosci. 2010, 30, 1385-1394). The B1 subunit binds the endogenous neurotransmitter ligand GABA as well as other orthosteric agonists (such as baclofen, SKF97541) and antagonists (such as phaclofen, saclofen). The B2 subunit is responsible for G-protein activation-mediated intracellular signal transduction and is believed to bind allosteric modulators (Binet et al, J Biol. Chem. 2004, 279, 29085-29091; Dupuis et al, Mol. Phannacol. 2006, 70, 2027-2036). The site of action for the Novartis GABAB positive allosteric modulator compounds CGP7930 and GS39783 is the heptahelical transmembrane domain of the B2 subunit; the exact binding site for other, unrelated positive allosteric modulator chemotypes is not known.
The main synaptic effects of GABAB receptors are the presynaptic blockade of neurotransmitter release (GABA as well as glutamate) and postsynaptic hyperpolarization (Gassmann and Bettler, in Handbook of Contemporary Neuropharmacology 2007). These effects are the result of inhibition of presynaptic calcium influx and stimulation of postsynaptic inwardly rectifying potassium (GIRK) channels, respectively. Ion channel functions are mediated in a membrane-delimited manner through the activation of βγ subunits of Gi/Go proteins. In addition to these, GABAB receptors also signal via the a subunit of the same G-proteins that inhibits adenylate cyclase and retards the recruitment of synaptic vesicles (Chalifoux and Carter, Curr. Opin. Neurobiol. 2011, 21, 339-442). Beside these fast cellular events, GABAB receptors also regulate cytoplasmic kinases including mitogen-activated protein kinase and thereby influence synaptic plasticity on the longer-term.
In order to better understand the physiological significance of GABAB receptors at the behavioral level, knockout mice have been generated with mutations selectively in the B1, B1a, B1b and the B2 subunits. Mice without B1 subunits displayed increased anxiety in explorative-like situations (light-dark box, staircase assays), increased panic, spontaneous seizures, hyperalgesia, hyperlocomotion, and memory impairment (Schuler et al, Neuron 2001, 31, 47-58). Mice that do not express GABAB2 subunits behave similarly to B1 subunit knockouts; these animals are overanxious, show spontaneous seizure activity, hyperalgesia, hyperlocomotion, and memory impairment (Mombereau et al, Eur. J Pharmacol. 2004, 497, 119-120; Mombereau et al, Neuroreport 2005, 16, 307-310; Gassmann et al, J Neurosci. 2004, 24, 6086-6097). Based on the above, the GABAB receptor system seems to play a general role in the regulation of neuronal excitability with consequences on various aspects of overt behavior.
The only approved and commercialized selective GABAB receptor ligand is the orthosteric agonist racemic baclofen. Baclofen was approved as a centrally acting muscle relaxant used to reduce spasticity associated with cerebral palsy, multiple sclerosis, and spinal cord injuries. Beside these applications, baclofen may have potential therapeutic benefits in treating conditions including asthma, pain, obesity, binge eating, drug and alcohol abuse, anxiety, posttraumatic stress disorder, cough, inflammation, gastroeasophageal reflux and urinary incontinence (eg., Breslow et al, Am. J Psychiatry 1989, 146, 353-356; Drake et al, Ann. Pharmacother. 2003, 37, 1177-1181; Leggio et al, CNS Neurol. Disord. Drug Targets 2010, 9, 33-44). Although baclofen has beneficial potential in a number of therapeutic indications, unfortunately it also has a range of unwanted properties including poor blood-brain-barrier penetration, narrow therapeutic window, receptor desensitization, development of tolerance against the main effects, and withdrawal upon termination of use (Vacher and Bettler, Curr. Drug Targets CNSNeurol. Disord. 2003, 2, 248-259; Ross et al, Neurocrit. Care 2011, 14, 103-108; Keegan et al, Neuropharmacology 2015, 95, 492-502).
Allosteric modulation is an alternative way to selectively stimulate GPCRs without the unwanted properties of orthosteric ligands (Conn et al, Nat Rev 2009, 8, 41-54; Wang et al, J. Pharmacol. Exp. Ther. 2009, 331, 340-348). Allosteric modulators bind to the receptors at sites that are different from the binding site of the endogenous (orthosteric) ligands and are effective predominantly if an agonist is also bound to the receptor. This has consequences on the temporal and spacial pattern of efficacy which in turn affects the behavioral and adaptive responses the organism gives to allosteric stimulation. In contrast to orthosteric agonism, allosteric modulation of targets is expected to show less side effects, desensitization and development of tolerance. Indeed, it has been shown for the GABAB receptor positive allosteric modulator GS39783 in preclinical models, that this compound can have a favourable side effect profile (Cryan et al, J. Pharmacol. Exp. Ther. 2004, 310, 952-963), desensitization of the receptor can be prevented (Gjoni and Urwyler, Neurophannacology 2008, 55:1293-1299) and tolerance may not develop upon chronic administration (Mombereau et al, Neuropsychophannacology 2004, 29, 1050-1062). These results suggest that positive allosteric modulators of the GABAB receptor may be useful novel chemical entities without the unwanted properties of the orthosteric ligands such as baclofen.
Several patents and patent applications describe positive allosteric GABAB modulators which have different chemical structures. Pyrimidine derivatives as positive allosteric modulators of the GABAB receptor have been disclosed in WO 2005/094828 and WO 2006/136442. Thieno[3,2-b]pyrimidine and [1,3]thiazolo[5,4-d]pyrimidine derivatives as positive allosteric modulators of the GABAB receptor have been disclosed in WO 2015/056771 (US 2015/0111876). Pyrazolo[1,5-a]pyrimidine derivatives have been disclosed in US 2016/0304527 A1.
In WO2017069270 Taisho Pharmaceutical Co., Ltd. described pyrazolo[1,5-a]pyrimidine and pyrazolo[1,5-a][1,3,5]triazine derivatives, as positive allosteric modulators at the GABAB receptors. In most of the examples the R1 substituent connects through a carbon-nitrogen bond to the core.
Two recent patent applications by Richter Gedeon Nyrt. (WO2018167629 and WO2018167630) describe pyrazolo-pyrimidines with positive allosteric activity at the GABAB receptors. These examples are carboxylic acids, and the heterocycle is connected to the pyrazolo[1,5-a]pyrimidine core through a nitrogen atom.
The purpose of the present invention is to provide further compounds with high affinity to GABAB receptors. Unexpectedly, we found in the present invention that compounds in which the central aromatic bicycle at position 7 is connected through a carbon atom to an optionally substituted six-membered saturated heterocyclic ring containing 1 or 2 heteroatom selected from N, O or S, show nanomolar potency. There is no suggestion in WO2018167629, WO2018167630 or WO2017069270 to undertake such structural modification to obtain the compounds of formula (I).
The structurally closest compounds disclosed in WO2017069270 by Taisho Pharmaceutical Co., Ltd. are examples A148, A225, B14, B23, B30, B31, B35. This patent suggests, that the sufficiently active compounds have a carbon-nitrogen bond between the core and the R1 substituent, or in the case of a carbon-carbon bond, the core needs an additional N atom at position X. These compounds (examples A148, A225, B14, B23, B30, B31, B35) are the less active compounds.
The skilled person would not expect that the present substitution on the pyrazolo[1,5-a]pyrimidine core keeps the excellent pharmaceutical activity.
The above described in vitro advantages are further strengthened by the unexpected finding that certain examples of the present invention possessed great behavioural benefit in the prenatal valproate disease model that recapitulates the core symptoms of autism spectrum disorder. The inventors therefore showed that the compounds of the invention has therapeutic potential for the core symptoms of autism spectrum disorder in humans.
Our invention discloses heterocyclic derivatives with a carbocyclic-pyrazolo-pyrimidine scaffold. We found that these compounds show mostly nanomolar potency.
We have identified a class of pyrazolo[1,5-a]pyrimidine derivatives which have high affinity for GABAB receptors providing unique role in the treatment of psychiatric, neurodevelopmental, neurological and other central nervous system disorders as well as peripheral conditions where stimulation of the GABAB receptor may offer therapeutic benefit.
We identified new compounds that are brain penetrant. The present invention relates to compounds being GABAB receptor positive allosteric modulators and the synthesis thereof. Compounds of the present invention are useful for the treatment of psychiatric, neurodevelopmental, neurological and other central nervous system disorders as well as peripheral conditions where stimulation of the GABAB receptor may offer therapeutic benefit.
The present invention relates to the pyrazolo[1,5-a] pyrimidine derivatives of formula (I)
The invention also relates to the pharmaceutical compositions containing the compounds of formula (I) or pharmaceutically acceptable salts, biologically active metabolites, pro-drugs, racemates, enantiomers, diastereomers, solvates and hydrates thereof.
Furthermore, the present invention relates to the synthesis of the compounds of formula (I) and optical antipodes or racemates and/or salts thereof, the pharmaceutical compositions comprising thereof and the chemical and pharmaceutical manufacture of medicaments containing these compounds, as well as the methods of treatment with these compounds, which means administering to a mammal to be treated—including human—suffering from psychiatric, neurodevelopmental, neurological and other central nervous system disorders as well as peripheral conditions where stimulation of the GABAB receptor may offer therapeutic benefit, effective amount of compounds of formula (I) and optical antipodes or racemates and/or salts thereof of the present invention as such or as medicament.
The present invention relates to the pyrazolo[1,5-a]pyrimidine derivatives of formula (I)
R1 represents phenyl- or cyclohexyl group substituted by C1-C6alkyl or halo-C1-C6alkyl;
R2 represents H or halogen;
R3 represents H or C1-C6alkyl;
R4 represents H; C1-C6alkyl or halo-C1-C6alkyl;
R5 and R6 may be each, independently H; C1-C6alkyl or halogen;
R7 and R8 may be each, independently H or C1-C6alkyl;
R9 and R10 may be each, independently H or C1-C6alkyl or R9 and R10 together may form oxo group;
X represents —CRxRy or —O— or —S(O)n— group, wherein Rx and Ry may be each, independently H or C1-C6alkyl group and wherein n is 0 or 1 or 2;
Z represents —NR—; or —O—; or —S(O)2— group wherein
R may be H or —C(O)R11 or —S(O)2R2 group; aminocarbonyl-C1-C3alkyl; carboxy-C1-C3alkyl; cyano-C1-C3alkyl; C1-C5(cyclo)alkyl; saturated 4-6 membered heterocyclic ring with one 0, or —C(NH)(NH2) group;
wherein R11 may be H; C1-C3alkyl; C1-C3alkoxy; deutero-C1-C3alkoxy; C1-C3alkoxy-C1-C3alkyl; C1-C3alkoxy-C1-C3alkoxy; methanesulphonyl-C1-C3alkyl; or R11 may be a saturated 3-6 membered carbocyclic ring, or a 4-6 membered saturated or unsaturated heterocyclic ring with one to three hetero atoms selected from N, O or S; or amino, mono- or dialkylamino group; amino-C1-C3alkyl; hydroxy-C1-C3alkyl substituted by NH2-group;
wherein R12 may be C1-C3alkyl; amino or dialkylamino group;
R4 and CRx may form a cycloalkyl ring;
or pharmaceutically acceptable salts, biologically active metabolites, pro-drugs, racemates, enantiomers, diastereomers, solvates and hydrates thereof.
The term “halogen” or “halo” as used herein alone or as a part of another group refers to chlorine, bromine, fluorine and iodine.
The term “C1-C6alkyl” as used herein refers to branched or straight chain alkyl groups comprising one to six carbon atoms, including but not limited to methyl, ethyl, propyl, normal- and isopropyl and different butyl groups.
The term “C1-C6alkoxy” as used herein refers to branched or straight chain alkyl groups comprising one to six carbon atoms bonded through an oxygen atom, including but not limited to, methoxy, ethoxy, n-propoxy, i-propoxy, and t-butoxy.
The term “mammal” as used herein refers to any members of the class “Mammalia” including, but not limited to human.
The term “salt” means nontoxic base addition salts of the compounds of the invention which are generally prepared by reacting the acid with a suitable organic or inorganic base.
Included within the scope of the present invention are all stereoisomers, geometric isomers and tautomeric forms of the compounds of formula (I), including compounds exhibiting more than one type of isomerism and mixtures of one or more thereof.
Conventional techniques for the preparation/isolation of individual enantiomers include chiral synthesis from the suitable optically pure precursor or resolution of the racemate (or racemate of a salt or derivative) using, for example chiral high pressure liquid chromatography (HPLC).
The term “pharmaceutically acceptable” describes an ingredient that is useful in preparing a pharmaceutical composition and is generally safe, non-toxic and neither biologically nor otherwise undesirable, and includes those acceptable for veterinary use as well as human pharmaceutical use.
The term “pharmaceutical composition” refers to a mixture of a compound of the invention with other chemical components, such as pharmaceutically acceptable auxiliary materials, e.g. diluents or carriers. The pharmaceutical composition facilitates administration of the compound to the subject.
The term “excipient” defines a chemical compound that facilitates the incorporation of a compound into cells or tissues.
As used herein, the term “treatment” means using an effective therapy to reduce, alleviate or eliminate the symptoms associated with diseases and conditions mediated and modulated by the GABAB receptor positive allosteric mechanism.
As a further aspect of the present invention there is provided the synthesis of compounds of formula (I).
Compounds according to the present invention were synthesized in line with the synthetic routes and schemes described below.
Accordingly, the compounds of formula (I) of the invention can be synthesized by one of the following routes:
If R9═R10═H; X═O and Z═NR then
If R4═R6=R8═R10═H; X═CRxRy; Ry═H and Z═NR then
If R4═H; X═CRxRy and Z═NR then
If Z═NR and X is not —S(O)n— then
If Z═O or —S(O)2— then
If X═S(O)2 and Z═NR then
If R9 and R10 together form an oxo group:
If R9═R10═H; X═O and Z═NR then: reacting β-amino-alcohol derivative of formula (II)
epichlorohydrin to provide a compound of formula (IV)
The so obtained morpholine derivative of formula (IV) is reacted with hydrogen and then with di-tert-butyl dicarbonate to provide a compound of formula (V)
The so obtained morpholine derivative of formula (V) is oxidized to carboxylic acid derivative of formula (VI)
If R4 is not H then:
Route a): reacting carboxylic acid ester derivative of formula (VII)
R4X (IX)
to provide the carboxylic acid derivative of formula (VII)
Route b): reacting carboxylic acid ester derivative of formula (VII)
trifluoromethanesulfonic anhydride to provide a compound of formula (XII)
The so obtained triflate derivative of formula (XII) is reacted with tetrabutylammonium fluoride to provide a compound of formula (XIII).
The so obtained fluoromethyl derivative of formula (XIII) is hydrolyzed to provide the carboxylic acid derivative of formula (VIII)
If R4═R6=R8═R10═H; X═CRxRy; Ry═H and Z═NR then reacting nicotinic acid derivative of formula (XIV) or nicotinic acid ester derivative of formula (XV)
If R4═H; X═CRxRy and Z═NR then reacting lactame derivative of formula (XVII)
The so obtained piperidine derivative of formula (XVIII) is reacted with hydrogen, then with di-tert-butyl dicarbonate to furnish piperidine derivative of formula (XIX)
The carboxylic acid ester is hydrolysed to provide piperidine derivative (XX).
Reacting a carboxylic acid ester derivative of formula (XXI) or carboxylic acid chloride derivative of formula (XXII)
If Z═NR and X is not S(O)n then reacting aminopyrazole derivative of formula (XXV) with either
The so obtained compound is treated with the appropriate reagents to furnish examples of formula (XXVIII)
Route c): reacting carboxylic acid derivative of formula (XXIX)
Route d): reacting carboxylic acid derivative of formula (XXIX)
is reacted with 1-Propynylmagnesium bromide to furnish alkyne derivative of formula (XXXIII).
If Z═O os S(O)2: reacting aminopyrazole derivative of formula (XXV) with the appropriate acetylacetone derivative or the appropriate alkyne derivative to furnish the pyrazolo[1,5-a]pyrimidine derivative of formula (XXXIV)
is chlorinated to furnish a chloro derivative of formula (XXXVII)
The so obtained compound is reacted with sulfone derivative of compound (XXXVII)
The so obtained compound is treated with the appropriate reagents to furnish examples of formula (XLI)
If R9 and R10 together form an oxo group: reacting chloro derivative of formula (XXXVII) with heterocycle of formula (XLII)
The synthesis of carboxylic acid derivative of formula (VI) can be carried out in the following way:
The reaction of β-amino-alcohol derivative of formula (II) with 4-Methoxybenzaldehyde is preferably carried out in a proper solvent, e.g. methanol. The reducing agent is preferably NaBH4. The reaction is carried out at a temperature in the range of 0° C. to room temperature. The necessary reaction time is 1-16 h. The reactions are followed by thin layer chromatography. The reaction is quenched by the addition of water. The product (III) is isolated by extraction with a proper organic solvent.
The ring closure of β-amino-alcohol derivative of formula (III) is preferably carried out in a suitable solvent, e.g. toluene with epichlorohydrin, suitable Lewis acid, e.g. LiClO4, and a suitable base, e.g. NaOMe in MeOH. The reaction is carried out at a temperature in the range of 0° C. to room temperature. The necessary reaction time is 24-48 h. The reactions are followed by thin layer chromatography. The reaction is quenched by the addition of saturated NH4Cl solution. The crude product is isolated by extraction with a proper organic solvent. The product (IV) is purified by column chromatography. The column chromatography is carried out on normal phase using Kieselgel 60 as adsorbent and different solvent systems, e.g. cyclohexane/ethyl acetate.
The hydrogenation of morpholine derivative of formula (IV) is preferably carried out in a suitable solvent, e.g. ethanol, in the presence of a suitable catalyst, e.g. palladium on carbon, in the presence of di-tert-butyl dicarbonate. The reaction is preferably carried out at room temperature, preferably at 5-10 bar. The necessary reaction time is 24-72 h. The reactions are followed by thin layer chromatography. The crude product is isolated after filtration over Celite pad. The product (V) is purified by column chromatography. The column chromatography is carried out on normal phase using Kieselgel 60 as adsorbent and different solvent systems, e.g. cyclohexane/ethyl acetate.
The oxidation of morpholine derivative of formula (V) is preferably carried out in a suitable solvent system, e.g. dichloromethane/water, preferably in the presence of TEMPO radical and (Diacetoxyiodo)benzene. The reaction is carried out at a temperature in the range of 0° C. to room temperature. The necessary reaction time is 1-16 h. The reactions are followed by thin layer chromatography. The crude product is isolated by extraction with a proper organic solvent. The product (VI) is crystallized from a suitable solvent, preferably hexane.
The synthesis of carboxylic acid derivative of formula (VIII) can be carried out by different routes:
The reaction of a carboxylic acid ester derivative of formula (VII) with an alkyl halide derivative of formula (IX) is preferably carried out in a proper solvent e.g. tetrahydrofuran, preferably in the presence of a strong base, e.g. lithium bis(trimethylsilyl)amide. The reaction is carried out at a temperature in the range of −78° C. to room temperature. The necessary reaction time is 1-16 h. The reactions are followed by thin layer chromatography. The reaction is quenched by the addition of saturated NH4Cl solution. The product (X) is isolated by extraction with a proper organic solvent.
The obtained carboxylic acid ester derivative of formula (X) is hydrolyzed in a suitable solvent mixture, e.g. ethanol/water, in the presence of an alkali, e.g. sodium hydroxide. The reaction is carried out at a temperature in the range of 0° C. to room temperature. The necessary reaction time is 1-16 h. The reactions are followed by thin layer chromatography. The reaction mixture is acidified to pH=3 with a suitable acid, e.g. citric acid. The product (VIII) is isolated by extraction with a proper organic solvent.
The reaction of a carboxylic acid ester derivative of formula (VII) with formaldehyde is preferably carried out in aproper solvent e.g. tetrahydrofuran, preferably in the presence of a strong base, e.g. lithium bis(trimethylsilyl)amide. The reaction is carried out at a temperature in the range of −78° C. to room temperature. The necessary reaction time is 1-16 h. The reactions are followed by thin layer chromatography. The reaction is quenched by the addition of saturated NH4Cl solution. The product (XI) is isolated by extraction with a proper organic solvent.
The triflation of hydroxymethyl derivative of formula (XI) with e.g. trifluoromethanesulfonic anhydride is preferably carried out in a proper solvent e.g. dichloromethane, preferably in the presence of a base, e.g. pyridine. The reaction is carried out at a temperature in the range of −78° C. to room temperature. The necessary reaction time is 1-16 h. The reactions are followed by thin layer chromatography. The reaction is quenched by the addition of 1M HCl solution. The product (XII) is isolated by extraction with a proper organic solvent.
The fluorination of triflate derivative of formula (XII) with tetrabutylammonium fluoride is preferably carried out in a proper solvent, e.g. tetrahydrofuran. The reaction is preferably carried out at room temperature. The necessary reaction time is 1-16 h. The reactions are followed by thin layer chromatography. The reaction is quenched by the addition of water. The crude product is isolated by extraction with a proper organic solvent. The product (XIII) is purified by column chromatography. The column chromatography is carried out on normal phase using Kieselgel 60 as adsorbent and different solvent systems, e.g. cyclohexane/ethyl acetate.
The obtained carboxylic acid ester derivative of formula (XIII) is hydrolyzed in a suitable solvent mixture, e.g. ethanol/water, in the presence of an alkali, e.g. sodium hydroxide. The reaction is carried out at a temperature in the range of 0° C. to room temperature. The necessary reaction time is 1-16 h. The reactions are followed by thin layer chromatography. The reaction mixture is acidified to pH=3 with a suitable acid, e.g. citric acid. The product (VIII) is isolated by extraction with a proper organic solvent.
The synthesis of carboxylic acid derivative of formula (XVI) can be carried out in the following way:
The reaction of nicotinic acid derivative of formula (XIV) or nicotinic acid ester derivative of formula with hydrogen is preferably carried out in a proper solvent, e.g. water or alcohol, in the presence of a proper catalyst, e.g. platinum(IV) oxide. The reaction is preferably carried out at room temperature, preferably at 5-10 bar. The necessary reaction time is 24-72 h. The reactions are followed by thin layer chromatography. The product is isolated after filtration over Celite pad. The reaction with di-tert-butyl dicarbonate is preferably carried out in a proper solvent or solvent system, e.g. tetrahydrofuran with water, optionally in the presence of a base, e.g. sodium bicarbonate. The product is isolated by extraction with a proper organic solvent. If the product is a carboxylic acid ester, it is hydrolyzed in a proper solvent system, e.g. ethanol/water, in the presence of an alkali, e.g. sodium hydroxide. The reaction is carried out at a temperature in the range of 0° C. to room temperature. The necessary reaction time is 1-16 h. The reactions are followed by thin layer chromatography. The reaction mixture is acidified to pH=3 with a suitable acid, e.g. citric acid. The product (XVI) is isolated by extraction with a proper organic solvent.
The synthesis of carboxylic acid derivative of formula (XX) can be carried out in the following way:
The reaction of lactam derivative of formula (XVII) with a proper reducing agent, e. g. NaBH4 with boron trifluoride diethyl etherate is preferably carried out in a proper solvent e.g. tetrahydrofuran. The reaction is carried out at a temperature in the range of −15° C. to room temperature. The necessary reaction time is 1-16 h. The reactions are followed by thin layer chromatography. The reaction is quenched by the addition of water. The product (XVIII) is isolated by extraction with a proper organic solvent.
The hydrogenation of piperidine derivative of formula (XVIII) is preferably carried out in a suitable solvent, e.g. methanol, in the presence of a suitable catalyst, e.g. palladium on carbon, in the presence of di-tert-butyl dicarbonate. The reaction is preferably carried out at room temperature, preferably at 5-10 bar. The necessary reaction time is 24-72 h. The reactions are followed by thin layer chromatography. The crude product is isolated after filtration over Celite pad. The product (XIX) is purified by column chromatography. The column chromatography is carried out on normal phase using Kieselgel 60 as adsorbent and different solvent systems, e.g. cyclohexane/ethyl acetate.
The obtained carboxylic acid ester derivative of formula (XIX) is preferably hydrolyzed in a suitable solvent, e.g. tetrahydrofuran, in the presence of potassium trimethylsilanolate. The reaction is carried out at a reflux temperature. The necessary reaction time is 1-16 h. The reactions are followed by thin layer chromatography. The reaction mixture is acidified to pH=4 with a suitable acid, e.g. citric acid. The product (XX) is isolated by extraction with a proper organic solvent.
The synthesis of aminopyrazole derivative of formula (XXV) can be carried out in the following way:
The reaction of a carboxylic acid ester derivative of formula (XXI) or carboxylic acid chloride derivative of formula (XXII) with an acetonitrile derivative of formula (XXIII) is preferably carried out in a proper solvent, e.g. tetrahydrofuran, preferably in the presence of a strong base e.g. n-butyllithium, lithium bis(trimethylsilyl)amide. The reaction carried out at a temperature in the range of −78° C. to room temperature. The necessary reaction time is 1-16 h. The reactions are followed by thin layer chromatography. The reaction mixture is quenched by addition of water and hydrochloric acid (˜pH 2-3) or saturated ammonium chloride solution. The product acylacetonitrile derivative of formula (XXIV) is isolated by extraction with a proper organic solvent.
The cyclocondensation reaction of the acylacetonitrile derivative of formula (XXIV) with hydrazine hydrate to aminopyrazole derivatives of formula (XXV) is preferably carried out in a suitable solvent, e.g. ethanol. The reaction is preferably carried out at boiling point of the solvent. The necessary reaction time is 1-6 h. The reactions are followed by thin layer chromatography. The reaction is quenched by the addition of water. The product (XXV) is isolated by extraction with a proper organic solvent.
The synthesis of pyrazolo[1,5-a]pyrimidine derivative of formula (XXVI) can be carried out in the following ways:
The cyclocondensation reaction of the aminopyrazole derivative of formula (XXV) with acetylacetone derivatives of formula (XXXI) is preferably carried out in a suitable solvent, e.g. toluene, in the presence of a proper catalyst, e.g. p-Toluenesulfonic acid monohydrate. The reaction is preferably carried out at boiling point of the solvent. The necessary reaction time is 1-16 h. The reactions are followed by thin layer chromatography. The product (XXVI) is purified by column chromatography. The column chromatography is carried out on normal phase using Kieselgel 60 as adsorbent and different solvent systems, e.g. cyclohexane/ethyl acetate.
The cyclocondensation reaction of the aminopyrazole derivative of formula (XXV) with alkyne derivatives of formula (XXXIII) is preferably carried out in a suitable solvent, e.g. ethanol, in the presence of a proper base, e.g. pyrrolidine, and a suitable acid, e.g. acetic acid. The reaction is preferably carried out at 60° C. The necessary reaction time is 4-16 h. The reactions are followed by thin layer chromatography. The product (XXVI) is purified by column chromatography. The column chromatography is carried out on normal phase using Kieselgel 60 as adsorbent and different solvent systems, e.g. cyclohexane/ethyl acetate.
The synthesis of pyrazolo[1,5-a]pyrimidine derivative of formula (XXVIII) can be carried out in the following way:
The reaction of pyrazolo[1,5-a]pyrimidine derivative of formula (XXVI) with a strong acid, e.g. trifluoroacetic acid is preferably carried out in a proper solvent, e.g. dichloromethane. The reaction carried out at a temperature in the range of 0° C. to room temperature. The necessary reaction time is 1-16 h. The reactions are followed by thin layer chromatography. The reaction mixture is quenched by addition of 2M sodium hydroxide solution (˜pH 12-14). The product pyrazolo[1,5-a]pyrimidine derivative of formula (XXVII) is isolated by extraction with a proper organic solvent.
The compound pyrazolo[1,5-a]pyrimidine derivative of formula (XXVII) can be transformed to pyrazolo[1,5-a]pyrimidine derivative of formula (XXVIII) in the following ways:
In certain embodiments the reaction of pyrazolo[1,5-a]pyrimidine derivative of formula (XXVII) with methyl bromoacetate, in the presence of a base, e.g. N,N-Diisopropylethylamine, is preferably carried out in a proper solvent, e.g. toluene. The reaction is preferably carried out at room temperature. The necessary reaction time is 4-16 h. The reactions are followed by thin layer chromatography. The reaction is quenched by the addition of water. The crude product is isolated by extraction with a proper organic solvent. The crude product is purified by column chromatography. The column chromatography is carried out on normal phase using Kieselgel 60 as adsorbent and different solvent systems, e.g. acetone/dichloromethane. The product is hydrolyzed in the presence of hydrochloric acid, in a suitable solvent, e.g. water, to furnish pyrazolo[1,5-a]pyrimidine derivative of formula (XXVIII).
In certain embodiments the reaction of pyrazolo[1,5-a]pyrimidine derivative of formula (XXVII) with N-Boc protected amino acids, in the presence of a base, e.g. NN-Diisopropylethylamine, is carried out in a proper solvent, e.g. dimethylformamide, using a proper coupling agent, e.g. HBTU. The reaction is preferably carried out at room temperature. The necessary reaction time is 1-16 h. The reactions are followed by thin layer chromatography. The reaction is quenched by the addition of water. The crude product is isolated by extraction with a proper organic solvent. The product is purified by column chromatography. The column chromatography is carried out on normal phase using Kieselgel 60 as adsorbent and different solvent systems, e.g. methanol/dichloromethane. The product is reacted with strong acid, e.g. Trifluoroacetic acid, in a proper solvent, e.g. dichloromethane. The reaction is preferably carried out at 0° C. to room temperature. The necessary reaction time is 1-16 h. The reactions are followed by thin layer chromatography. The product (XXVIII) is purified by column chromatography. The column chromatography is carried out on normal phase using Kieselgel 60 as adsorbent and different solvent systems, e.g. methanol/dichloromethane.
In certain embodiments the reaction of pyrazolo[1,5-a]pyrimidine derivative of formula (XXVII) with acyl chlorides, in the presence of a base, e.g. triethylamine, is preferably carried out in a proper solvent, e.g. dichloromethane. The reaction is preferably carried out at 0° C. to room temperature. The necessary reaction time is 1-16 h. The reactions are followed by thin layer chromatography. The reaction is quenched by the addition of water. The crude product is isolated by extraction with a proper organic solvent. The product (XXVIII) is purified by column chromatography. The column chromatography is carried out on normal phase using Kieselgel 60 as adsorbent and different solvent systems, e.g. methanol/dichloromethane.
In certain embodiments the reaction of pyrazolo[1,5-a]pyrimidine derivative of formula (XXVII) with formic acid, is preferably carried out in a proper solvent, e.g. toluene. The reaction is preferably carried out at boiling point of the solvent. The necessary reaction time is 4-16 h. The reactions are followed by thin layer chromatography. The reaction is quenched by the addition of water. The crude product is isolated by extraction with a proper organic solvent. The product (XXVIII) is purified by column chromatography. The column chromatography is carried out on normal phase using Kieselgel 60 as adsorbent and different solvent systems, e.g. methanol/dichloromethane.
In certain embodiments the reaction of pyrazolo[1,5-a]pyrimidine derivative of formula (XXVII) with carboxylic acids, in the presence of a base, e.g. N,N-Diisopropylethylamine, is carried out in a proper solvent, e.g. dimethylformamide, using a proper coupling agent, e.g. HBTU. The reaction is preferably carried out at room temperature. The necessary reaction time is 1-16 h. The reactions are followed by thin layer chromatography. The reaction is quenched by the addition of water. The crude product is isolated by extraction with a proper organic solvent. The product (XXVIII) is purified by column chromatography. The column chromatography is carried out on normal phase using Kieselgel 60 as adsorbent and different solvent systems, e.g. methanol/dichloromethane.
In certain embodiments the reaction of pyrazolo[1,5-a]pyrimidine derivative of formula (XXVII) with 1-Amidinopyrazole Hydrochloride, in the presence of a base, e.g. N,N-Diisopropylethylamine, is preferably carried out in a proper solvent, e.g. dimethylformamide. The reaction is preferably carried out at room temperature. The necessary reaction time is 1-16 h. The reactions are followed by thin layer chromatography. The product (XXVIII) is isolated by filtration.
In certain embodiments the reaction of pyrazolo[1,5-a]pyrimidine derivative of formula (XXVII) with the proper aldehyde or ketone, in the presence of a reducing agent, e.g. Sodium triacetoxyborohydride, in the presence of acetic acid, is preferably carried out in a proper solvent, e.g. 1,2-Dichloroethane. The reaction is preferably carried out at room temperature. The necessary reaction time is 1-16 h. The reactions are followed by thin layer chromatography. The reaction is quenched by the addition of water. The crude product is isolated by extraction with a proper organic solvent. The product (XXVIII) is purified by column chromatography. The column chromatography is carried out on normal phase using Kieselgel 60 as adsorbent and different solvent systems, e.g. methanol/dichloromethane.
In certain embodiments the reaction of pyrazolo[1,5-a]pyrimidine derivative of formula (XXVII) with (Trimethylsilyl)isocyanate, is preferably carried out in a proper solvent, e.g. dichloromethane. The reaction is preferably carried out at room temperature. The necessary reaction time is 1-16 h. The reactions are followed by thin layer chromatography. The reaction is quenched by the addition of water. The crude product is isolated by extraction with a proper organic solvent. The product (XXVIII) is purified by column chromatography. The column chromatography is carried out on normal phase using Kieselgel 60 as adsorbent and different solvent systems, e.g. methanol/dichloromethane.
In certain embodiments the reaction of pyrazolo[1,5-a]pyrimidine derivative of formula (XXVII) with sulfamide, is preferably carried out in a proper solvent, e.g. dioxane. The reaction is preferably carried out at boiling point of the solvent. The necessary reaction time is 1-16 h. The reactions are followed by thin layer chromatography. The reaction is quenched by the addition of water. The crude product is isolated by extraction with a proper organic solvent. The product (XXVIII) is purified by column chromatography. The column chromatography is carried out on normal phase using Kieselgel 60 as adsorbent and different solvent systems, e.g. methanol/dichloromethane.
The compounds of the present invention and optical antipodes or racemates and/or salts thereof can be used as such or suitably in the form of pharmaceutical compositions.
The invention also relates to the pharmaceutical compositions containing the compounds of formula (I) or optical antipodes or racemates and/or salts thereof as active ingredient for the treatment of certain disorders associated with GABAB receptor positive allosteric modulator activity.
The present compounds may be co-adminstered to a subject in combination with two or more different therapeutic agents (eg. most preferably antipsychotics and psychostimulants; and preferably antidepressants, anxiolytics, antihypertensives, anticonvulsants, sedatives, and narcotics).
Suitable routes of administration may, for example, include oral, rectal, transmucosal, transdermal or intestinal administration; parenteral delivery, including intramuscular, subcutaneous, intravenous, intramedullary injections, as well as intraarticular, intrathecal, direct intraventricular, intraperitoneal, intranasal, or intraocular injections and eye drops.
Alternatively, one may administer the compound in a local rather than systemic manner, for example, via injection of the compound directly in the renal or cardiac area, often in a depot or sustained release formulation. Furthermore, one may administer the drug in a targeted drug delivery system, for example, in a liposome coated with a tissue-specific antibody. The liposomes will be targeted to and taken up selectively by the organ.
The pharmaceutical compositions can be administered through via a variety of routes and dosages forms. The compound of the invention may be administered either alone or in combination with pharmaceutically acceptable carriers, in either single or multiple doses. The dosage required to exert the therapeutic effect can vary within wide limits and will be fitted to the individual requirements in each of the particular case, depending on the stage of the disease, the condition and the bodyweight of the patient to be treated, as well as the sensitivity of the patient against the active ingredient, route of administration and number of daily treatments.
For the sake of a simple administration it is suitable if the pharmaceutical compositions comprise dosage units containing the amount of the active ingredient to be administered once, or a few multiples or a half, third or fourth part thereof. Such dosage units are e.g. tablets, which can be powdered with grooves promoting the halving or quartering of the tablet in order to exactly administer the required amount of the active ingredient.
The pharmaceutical compositions containing the active ingredient according to the present invention usually contain 0.01 to 500 mg of active ingredient in a single dosage unit. It is, of course possible that the amount of the active ingredient in some compositions exceeds the upper or lower limits defined above.
As a further aspect of the invention there is provided the pharmaceutical manufacture of medicaments containing the compounds of formula (I) or optical antipodes or racemates and/or salts thereof.
The pharmaceutical compositions of the present invention may be formulated as different pharmaceutical dosage forms, such as but not limited to, solid oral dosage forms like tablets (e.g. buccal, sublingual, effervescents, chewable, orodispersible, freeze dried), capsules, lozenges, pastilles, pills, orodispersible films, granules, powders; liquid oral dosage forms like solutions, emulsions, suspensions, syrups, elixirs, oral drops; parenteral dosage forms like intravenous injections, intramuscular injections, subcutaneous injections; other dosage forms like eye drops, semi-solid eye preparations, transdermal dosage forms, suppositories, rectal capsules, rectal solutions, emulsions and suspensions, etc.
In one embodiment the invention relates to pharmaceutical dosage forms specifically intended for pediatric use, such as but not limited to, solutions, syrups, elixirs, suspensions, powders for reconstitution as suspension, dispersible or effervescent tablets, chewable tablets, orally disintegrating tablets, tablets or coated tablets, sprinkle oral powder or granules, capsules.
The pharmaceutical compositions of the present invention may be manufactured in a manner that is itself known, e.g., by means of conventional mixing, dissolving, emulsifying, suspending, entrapping, freeze-drying, extrusion, laminating, film-casting, granulating, grinding, encapsulating, dragee-making or tableting processes.
Pharmaceutical compositions for use in accordance with the present invention thus may be formulated in conventional manner using one or more physiologically acceptable carriers comprising excipients and auxiliaries which facilitate processing of the active compounds into preparations which can be used pharmaceutically. Proper formulation is dependent upon the route of administration chosen. Any of the well-known techniques, carriers, and excipients may be used as suitable and as understood in the art.
Suitable excipients for the preparation of the dosage forms may be selected from the following categories, such as but not limited to, tablet and capsule fillers, tablet and capsule binders, modified-release agents, disintegrants, glidants, lubricants, sweetening agents, taste-masking agents, flavoring agents, coating agents, surfactants, antioxidants, buffering agents, complexing agents, emulsifying agents, lyophilization aids, microencapsulating agents, ointment bases, penetration enhancers, solubilizing agents, solvents, suppository bases, suspending agents.
In one embodiment the invention relates to the using of specific excipients which are able to improve the solubility, dissolution, penetration, adsorption or bioavailability of the active ingredient(s), such as but not limited to, hydrophilic polymers, hot melt extrusion excipients, surfactants, buffering agents, complexing agents, emulsifying agents, lyophilization aids, superdisintegrants, microencapsulating agents, penetration enhancers, solubilizing agents, co-solvents, suspending agents.
The above described ingredients and different routes of manufacture are merely representative. Other materials as well as processing techniques and the like well known in the art can also be used.
The compounds are effective in the treatment of psychiatric, neurodevelopmental, neurological and other central nervous system disorders as well as peripheral conditions where stimulation of the GABAB receptor may offer therapeutic benefit
Cortices of freshly harvested rat brains were dissected on an ice-cold surface and homogenized by a glass Dounce homogeniser immediately in ice-cold buffer containing 50 mM Tris, 5 mM MgCl2 and 1 mM EDTA (pH=7.6). Tissue homogenates were centrifuged at 40000 g for 15 min at 4° C. Membrane pellets were resuspended in the same buffer and membranes were incubated for 10 min at 30° C. in a shaking water bath to eliminate endogenous GABA. Homogenates were centrifuged again under the same conditions. The final pellets were resuspended in ice-cold buffer (pH=7.6) containing 50 mM Tris, 100 mM NaCl, 7 mM MgCl2, 1 mM EDTA and 1 mM dithiotreithol (DTT) to yield a concentration of 20 mg tissue weight/ml and frozen at −70° C. until use. The assay was done in a buffer containing 50 mM Tris (pH=7.4), 100 mM NaCl, 7 mM MgCl2, 1 mM EDTA and 1 mM DTT. Each assay tube contained 150 μL GDP (in a final concentration of 50 μM), 100 μL ligand and 125 μL of the membrane suspension (250 μg tissue/tube). The assay tubes were preincubated for 10 min at 30° C. to assure equilibrium. Nonspecific binding was determined in the presence of 10 μM GTPγS; basal binding was determined in the presence of buffer only. After addition of 50 μM [35S]GTPγS in a volume of 25 μL to the tubes, membranes were incubated for an additional 60 min at 30° C. The assay was terminated by rapid filtration through Packard UniFilter GF/B using a Packard harvester and washed four times with 1 ml ice-cold buffer. After drying the filters at 40° C. for 1 h, 40 μL Microscint (Packard) was added to the filters and radioactivity of the filters was determined by a TopCount NXT (PerkinElmer, Waltham, Mass.; Alper and Nelson, Eur. J. Pharmacol. 1998, 343, 303-312; Rinken et al, Biochem. Pharmacol. 1999, 57, 155-162). Data thus gathered were used to determine PAM EC50 values for each compound as primary in vitro activity end point.
In Table 1 compounds of this invention measured in the [35S]GTPγS binding assay are listed.
Under stressful conditions, adult rats emit 22 kHz ultrasounds that can be reduced by various pharmacological treatments (De Vry et al, Eur. J. Pharmacol. 1993, 249, 331-339; Sanchez, Eur. J. Pharmacol. 2003, 463, 133-143). Previous unpublished experiments indicated that GABAB receptor ligands can also inhibit vocalizations that are induced by electric footshocks as stressor. Therefore, a foot shock-induced vocalization paradigm in adult rats was used to assess in vivo efficacy of centrally acting GABAB receptor ligands. Behavioral measurements were carried out on male Wistar rats (200-250 g, Toxicoop, Hungary or Janvier, France). Rats were housed in groups of four in plastic cages with a wire grid top in a temperature and light-controlled laboratory animal care unit (22±2° C., 12-h light/dark cycle, lights on at 6:00 AM) with ad libitum access to commercial pellet rat food and tap water. Investigations were approved by the Local Ethical Committee of Gedeon Richter Plc. and were carried out in strict compliance with the European Directive 2010/63/EU regarding the care and use of laboratory animals for experimental procedures and all efforts were made to minimize the number of animals as well as their suffering. In order to evoke emission of ultrasounds, animals were footshocked after a habituation period of 30 s (6 shocks, 1 s, 0.8 mA each, inter-shock interval 10 s) in a sound attenuated shocking chamber (Experimetria, 40×40×80 cm). Investigational compounds were administered at the dose of 10 mg/kg in a solid dispersion formulation or Tween80 suspension in distilled water 1 h before shocking per os. Vocalizations were measured right after the last footshock for 10 min with a Metris Sonotrack system and the total time of vocalizations was registered. Vocalization of parallel vehicle treated animals was considered as control value and inhibition percent was calculated for each compound.
In Table 2 compounds of this invention measured in the USV assay are listed.
The prenatal valproate model has excellent construct and face validity, therefore it is a widely accepted disease model of ASD (Christensen et al, JAMA 2013, 309, 1696-1703; Roullet et al, Neurotox. Teratol. 2013, 36, 45-56). In this method, time-mated female Wistar rats (Harlan UK) were administered a single dose of valproic acid (VPA, 600 mg/kg, i.p.) on gestational day 12.5. Male offspring were housed according to standard laboratory conditions until time of testing at postnatal day 59. Animals were housed in groups of 4 in conventional cages and maintained at 22-24° C. on a standard 12 hour light/dark cycle (07.30-19.30), with food and water available ad libitum. After investigational drug treatment, offspring were examined behaviorally in the social preference assay at postnatal day 59. The social preference test is a highly accepted assay to assess autistic behavior in rodents (Nadler et al, Genes Brain Behav. 2007, 3, 303-314; Bambini-Junior et al, Brain Res. 2011, 1408, 8-16). Briefly, in this assay a test animal is allowed to investigate a conspecific separated by a dividing perforated wall or a similar area however, without a target conspecific. An autistic animal (such as a prenatally valproate-exposed rat) spends little time with social investigation during a test session.
The inventors unexpectedly found that examples of the present invention were of great behavioral benefit in the present preclinical disease model that recapitulates the core symptoms of ASD. The inventors therefore showed that these compounds may be of therapeutic potential for the core symptoms of ASD in humans.
The invention is further defined in the following Examples. It should be understood that the Examples are given by way of illustration only. From the above discussion and the Examples, one skilled in the art can ascertain the essential characteristics of the invention, and without departing from the spirit and scope thereof, can make various changes and modifications to adapt the invention to various uses and conditions. As a result, the invention is not limited by the illustrative examples set forth herein below, but rather defined by the claims appended hereto.
In general, the compounds of formula (I) can be prepared according to the general knowledge of one skilled in the art and/or using methods set forth in the Example and/or Intermediate sections that follow. Solvents, temperatures, pressures, and other reaction conditions can readily be selected by one of ordinary skill in the art. Starting materials are commercially available and/or readily prepared by one skilled in the art.
The present invention will be now illustrated by the following not limiting examples.
Under nitrogen to a solution of 6.00 g (80 mmol) (R)-2-Amino-1-propanol in 60 ml methanol was added 10.3 g (75.9 mmol) 4-Methoxybenzaldehyde. After addition the mixture was stirred at RT for 3 hours, then 3.02 g (80 mmol) NaBH4 was added in portions at 0° C. The obtained mixture was allowed to warm to RT and stirred at this temperature for 18 hours.
The reaction mixture was quenched by slow addition of 70 ml distilled water at 0° C. Methanol was evaporated, and the resulting mixture was extracted with dichloromethane. The combined organic layer was washed with distilled water, dried over anhydrous sodium sulfate, filtered and concentrated in vacuo to yield 13.77 g (88%) of the title compound. GC-MS (EI) m/z 196.2 [MH+]
The above obtained (2R)-2-{[(4-methoxyphenyl)methyl]amino}propan-1-ol was suspended in 100 ml toluene and 3.98 g (43 mmol) (R)-Epichlorohydrin was added, followed by the addition of 4.58 g (43 mmol) LiClO4. The reaction mixture was stirred at RT for 18 hours, then 30 ml sodium methoxide solution was added (25 wt % in CH3OH). The reaction mixture was stirred at RT for 18 hours. 100 ml saturated aqeuous NH4Cl was added, followed by the addition of 30 ml distilled water. The mixture was extracted with ethyl acetate. The combined organic layer was washed with distilled water, brine, dried over anhydrous sodium sulfate, filtered and concentrated in vacuo. The crude product was purified by silica gel chromatography eluting with 0-100% ethyl acetate in cyclohexane to yield 4.01 g (52%) of the title compound. GC-MS (EI) m/z 252.2 [MH]
The above obtained [(2S,5R)-4-[(4-methoxyphenyl)methyl]-5-methylmorpholin-2-yl]methanol was dissolved in 100 ml ethanol, and hydrogenated at 10 bar in the presence of 500 mg 10% Pd/C and 5.22 g (23.9 mmol) BOC2O for 2 days at RT. The reaction mixture was filtered through Celite, concentrated in vacuo, and purified by silica gel chromatography eluting with 0-100% ethyl acetate in cyclohexane to yield 1.55 g (42%) of the title compound. GC-MS (EI) m/z 232.2 [MH]
The above obtained tert-butyl (2S,5R)-2-(hydroxymethyl)-5-methylmorpholine-4-carboxylate was dissolved in 50 ml dichloromethane and 25 ml distilled water. To the reaction mixture was added 210 mg (1.34 mmol) TEMPO and 4.97 g (15.4 mmol) (Diacetoxyiodo)benzene at 0° C. The obtained mixture was allowed to warm to RT and stirred at this temperature for 18 hours. The reaction was quenched by the addition of 10 ml methanol. The mixture was extracted with dichloromethane. The combined organic layer was washed with distilled water, brine, dried over anhydrous sodium sulfate, filtered and concentrated in vacuo. The residue was triturated with hexane and filtered to yield 1.02 g (62%) of the title compound. GC-MS (EI) m/z 246.1 [MH]
The title compound is prepared from (2R)-2-{[(4-methoxyphenyl)methyl]amino}propan-1-ol and (S)-Epichlorohydrin according to the method described in Intermediate 1b.
The title compound is prepared from [(2R,5R)-4-[(4-methoxyphenyl)methyl]-5-methylmorpholin-2-yl]methanol according to the method described in Intermediate 1c.
The title compound is prepared from tert-butyl (2R,5R)-2-(hydroxymethyl)-5-methylmorpholine-4-carboxylate according to the method described in Intermediate 1d.
The title compound is prepared from (S)-2-Amino-1-propanol according to the method described in Intermediate 1a.
The title compound is prepared from (2S)-2-{[(4-methoxyphenyl)methyl]amino}propan-1-ol and (S)-Epichlorohydrin according to the method described in Intermediate 1b.
The title compound is prepared from tert-butyl [(2R,5S)-4-[(4-methoxyphenyl)methyl]-5-methylmorpholin-2-yl]methanol according to the method described in Intermediate 1c.
The title compound is prepared from tert-butyl (2R,5S)-2-(hydroxymethyl)-5-methylmorpholine-4-carboxylate according to the method described in Intermediate 1d.
The title compound is prepared from (2S)-2-{[(4-methoxyphenyl)methyl]amino}propan-1-ol and (R)-Epichlorohydrin according to the method described in Intermediate 1b.
The title compound is prepared from [(2S,5S)-4-[(4-methoxyphenyl)methyl]-5-methylmorpholin-2-yl]methanol according to the method described in Intermediate 1c.
The title compound is prepared from tert-butyl (2S,5S)-2-(hydroxymethyl)-5-methylmorpholine-4-carboxylate according to the method described in Intermediate 1d.
The title compound is prepared from 2-amino-2-methylpropan-1-ol according to the method described in Intermediate 1a.
The title compound is prepared from 2-(benzylamino)-2-methylpropan-1-ol and (R)-Epichlorohydrin according to the method described in Intermediate 1b.
The title compound is prepared from tert-butyl [(2S)-4-benzyl-5,5-dimethylmorpholin-2-yl]methanol according to the method described in Intermediate 1c.
The title compound is prepared from tert-butyl (2S)-2-(hydroxymethyl)-5,5-dimethylmorpholine-4-carboxylate according to the method described in Intermediate 1d.
The title compound is prepared from 2-(benzylamino)-2-methylpropan-1-ol and (S)-Epichlorohydrin according to the method described in Intermediate 1b.
The title compound is prepared from tert-butyl [(2R)-4-benzyl-5,5-dimethylmorpholin-2-yl]methanol according to the method described in Intermediate 1c.
The title compound is prepared from tert-butyl (2R)-2-(hydroxymethyl)-5,5-dimethylmorpholine-4-carboxylate according to the method described in Intermediate 1d.
The title compound is prepared from (R)-1-Amino-2-propanol according to the method described in Intermediate 1a.
The title compound is prepared from (2R)-1-{[(4-methoxyphenyl)methyl]amino}propan-2-ol and (S)-Epichlorohydrin according to the method described in Intermediate 1b.
The title compound is prepared from tert-butyl [(2R,6R)-4-[(4-methoxyphenyl)methyl]-6-methylmorpholin-2-yl]methanol methanol according to the method described in Intermediate 1c.
The title compound is prepared from tert-butyl (2R,6R)-2-(hydroxymethyl)-6-methylmorpholine-4-carboxylate according to the method described in Intermediate 1d.
The title compound is prepared from (S)-1-Amino-2-propanol according to the method described in Intermediate 1a.
The title compound is prepared from (2S)-1-{[(4-methoxyphenyl)methyl]amino}propan-2-ol and (R)-Epichlorohydrin according to the method described in Intermediate 1b.
The title compound is prepared from tert-butyl [(2S,6S)-4-[(4-methoxyphenyl)methyl]-6-methylmorpholin-2-yl]methanol methanol according to the method described in Intermediate 1c.
The title compound is prepared from tert-butyl (2S,6S)-2-(hydroxymethyl)-6-methylmorpholine-4-carboxylate according to the method described in Intermediate 1d.
The title compound is prepared from (2S)-1-{[(4-methoxyphenyl)methyl]amino}propan-2-ol and (S)-Epichlorohydrin according to the method described in Intermediate 1b.
The title compound is prepared from [(2R,5S)-4-[(4-methoxyphenyl)methyl]-6-methylmorpholin-2-yl]methanol according to the method described in Intermediate 1c.
The title compound is prepared from tert-butyl (2R,6S)-2-(hydroxymethyl)-6-methylmorpholine-4-carboxylate according to the method described in Intermediate 1d.
The title compound is prepared from (S)-2-Amino-3-methyl-1-butanol according to the method described in Intermediate 1a.
The title compound is prepared from (2S)-2-{[(4-methoxyphenyl)methyl]amino}-3-methylbutan-1-ol and (S)-Epichlorohydrin according to the method described in Intermediate 1b.
The title compound is prepared from [(2R,5S)-4-[(4-methoxyphenyl)methyl]-5-(propan-2-yl)morpholin-2-yl]methanol according to the method described in Intermediate 1c.
The title compound is prepared from tert-butyl (2R,5S)-2-(hydroxymethyl)-5-(propan-2-yl)morpholine-4-carboxylate according to the method described in Intermediate 1d.
The title compound is prepared from (2S)-2-{[(4-methoxyphenyl)methyl]amino}propan-1-ol and (R)-Epichlorohydrin according to the method described in Intermediate 1b.
The title compound is prepared from [(2S,5S)-4-[(4-methoxyphenyl)methyl]-5-methylmorpholin-2-yl]methanol according to the method described in Intermediate 1c.
The title compound is prepared from tert-butyl (2S,5S)-2-(hydroxymethyl)-5-(propan-2-yl)morpholine-4-carboxylate according to the method described in Intermediate 1d.
The title compound is prepared as described in Tetrahedron, 2010, 66, 5492-5497.
The title compound is prepared as described in WO2015/164508.
Under nitrogen to a solution of 2.18 g (7.8 mmol) 1-tert-butyl 3-methyl 5,5-difluoropiperidine-1,3-dicarboxylate (prepared as described in WO2015/164508) in 50 ml dry tetrahydrofuran 8.6 mL 1 M lithium bis(trimethylsilyl)amide in tetrahydrofuran solution (8.6 mmol) was added dropwise at (−78) ° C.—(−65) ° C. After addition the mixture was stirred at −78° C. for 1 hour, 0.73 mL (11.7 mmol) of Iodomethane was added dropwise. The so obtained mixture was allowed to warm to RT and stirred at this temperature for 18 h. The reaction mixture was quenched by addition of 25 ml saturated ammonium chloride solution and 10 ml distilled water. The reaction mixture was extracted with ethyl acetate, the combined organic layer was washed with distilled water, brine, dried over anhydrous sodium sulfate, filtered and concentrated in vacuo to yield 2.22 g (97%) of the title compound. GC-MS (EI) m/z 294.1 [MH+]
The above obtained tert-butyl 1-tert-butyl 3-methyl 5,5-difluoro-3-methylpiperidine-1,3-dicarboxylate was dissolved in 30 ml methanol. 30.3 ml 2 M aqeuous sodium hydroxide (15.1 mmol) was added dropwise at 0° C. The obtained mixture was allowed to warm to RT and stirred at this temperature for 18 hours. The reaction mixture was acidified to pH=3 with citric acid, and methanol was evaporated. The mixture was extracted with ethyl acetate. The combined organic layer was washed with distilled water, brine, dried over anhydrous sodium sulfate, filtered and concentrated in vacuo to yield 2.20 g (100%) of the title compound. GC-MS (EI) m/z 280.1 [MH]
The title compound is prepared as described in WO2011/26917.
A solution of 15 g (86.6 mmol) 4-methylpyridine-3-carboxylic acid hydrochloride in 100 ml distilled water was hydrogenated at 10 bar in the presence of 1.5 g PtO2×H2O for 12 hours at RT. The mixture was filtered through Celite and concentrated in vacuo to yield 16.6 g (100%) of the title compound.
33.29 g (185.3 mmol) of cis-4-methylpiperidine-3-carboxylic acid was dissolved 300 ml distilled water and 200 ml tetrahydrofuran. 39.3 g (371 mmol) Na2CO3 was added, followed by the addition of 40.4 g (185 mmol) BOC2O dissolved in 100 ml tetrahydrofuran, at 0° C. The obtained mixture was allowed to warm to RT and stirred at this temperature for 18 hours. The reaction mixture was acidified to pH=3 with citric acid. The mixture was extracted with ethyl acetate. The combined organic layer was washed with distilled water, brine, dried over anhydrous sodium sulfate, filtered and concentrated in vacuo to yield 29.40 g (65%) of the title compound. GC-MS (EI) m/z 243.2 [MH+]
To a solution of 1.22 g (5 mmol) cis-1-[(tert-butoxy)carbonyl]-4-methylpiperidine-3-carboxylic acid (Intermediate 15) in 6 ml dimethylformamide was added 6.52 g (20 mmol) Cs2CO3 and 2.5 ml (40 mmol) iodomethane. The obtained mixture was stirred at RT for 18 hours. 50 ml distilled water was added. The mixture was extracted with ethyl acetate. The combined organic layer was washed with distilled water, brine, dried over anhydrous sodium sulfate, filtered and concentrated in vacuo to yield 1.29 g (100%) of the title compound. GC-MS (EI) m/z 258.2 [MH+]
Under nitrogen to a solution of 0.76 g (3 mmol) 1-tert-butyl 3-methyl cis-4-methylpiperidine-1,3-dicarboxylate in 25 ml dry tetrahydrofuran 10 mL 1 M potassium tert-butoxy in tetrahydrofuran solution (10 mmol) was added dropwise at (−78) ° C.-(−65) ° C. After addition the mixture was stirred at −78° C. for 2 hours, 8 mL distilled water, 8 ml methanol, 5 ml 10 M aqeuous sodium hydroxide (50 mmol) was added dropwise. The reaction mixture was allowed to warm to RT, and stirred for 2 hours. The reaction mixture was acidified to pH=3 with citric acid, and methanol was evaporated. The obtained mixture was extracted with ethyl acetate. The combined organic layer was washed with distilled water, brine, dried over anhydrous sodium sulfate, filtered and concentrated in vacuo. The residue was dissolved in ethyl acetate and ethanolic ammonia was added. The precipitated crystals were filtered, partitioned between 10% citric acid solution and ethyl acetate. The mixture was extracted with ethyl acetate. The combined organic layer was washed with distilled water, brine, dried over anhydrous sodium sulfate, filtered and concentrated in vacuo to yield 0.59 g (82%) of the title compound. GC-MS (EI) m/z 244.1 [MH+]
The title compound is prepared from 4-ethylpyridine-3-carboxylic acid according to the method described in Intermediate 16a.
The title compound is prepared from 4-ethylpiperidine-3-carboxylic acid hydrochloride according to the method described in Intermediate 16b.
To a suspension of 7.1 g (34.2 mmol) ethyl (3S)-3-methylpiperidine-3-carboxylate hydrochloride (prepared as described in WO 2018/167631) in 100 ml dichloromethane was added 10.5 ml (75.2 mmol) triethylamine, and 8.21 g (37.6 mmol) BOC2O at 0° C. The resulting mixture was allowed to warm to RT and stirred for 3 hours. The reaction mixture was washed with distilled water, 10% citric acid solution, brine, and concentrated in vacuo to yield 9.68 g (104%) of the title compound. GC-MS (EI) m/z 272.2 [MH]
The above obtained 1-tert-butyl 3-ethyl (3S)-3-methylpiperidine-1,3-dicarboxylate was dissolved in 200 ml ethanol and 65 ml 4 M aqueous sodium hydroxide (300 mmol) was added dropwise at 0° C. The reaction mixture was allowed to warm to RT, and stirred for 18 hours. The reaction mixture was acidified to pH=3 with citric acid, and ethanol was evaporated. The obtained mixture was extracted with ethyl acetate. The combined organic layer was washed with distilled water, brine, dried over anhydrous sodium sulfate, filtered and concentrated in vacuo to yield 8.0 g (96%) of the title compound. GC-MS (EI) m/z 244.1 [MH+]
The title compound is prepared from (3R)-3-methylpiperidine-3-carboxylate hydrochloride (prepared as described in WO 2018/167631) according to the method described in Intermediate 19a.
The title compound is prepared from 1-tert-butyl 3-ethyl (3R)-3-methylpiperidine-1,3-dicarboxylate according to the method described in Intermediate 19a.
Under nitrogen to a solution of 2.20 g (8 mmol) methyl 1-benzyl-4,4-dimethyl-6-oxopiperidine-3-carboxylate (prepared as described in J. Org. Chem. 2005, 70, 3957-3962.) in 22 ml dry tetrahydrofuran was added 0.92 g (24.4 mmol) NaBH4 and 3.96 ml boron trifluoride diethyl etherate dropwise at −15° C. The reaction mixture was allowed to warm to RT, and stirred for 3 hours. 15 ml distilled water was added and the reaction mixture was extracted with ethyl acetate, the combined organic layer was washed with distilled water, brine, dried over anhydrous sodium sulfate, filtered and concentrated in vacuo to yield 1.87 g (89%) of the title compound. GC-MS (EI) m/z 262.2 [MH]
The above obtained methyl 1-benzyl-4,4-dimethylpiperidine-3-carboxylate was dissolved in 20 ml methanol and hydrogenated at 10 bar in the presence of 0.4 g 10% Pd/C and 1.60 g (7.1 mmol) BOC2O at RT for 18 hours. The reaction mixture was filtered through Celite, concentrated in vacuo, and purified by silica gel chromatography eluting with 20% ethyl acetate in cyclohexane to yield 0.89 g (47%) of the title compound. GC-MS (EI) m/z 271.2 [MH]
To a solution of 0.48 g (1.9 mmol) 1-tert-butyl 3-methyl 4,4-dimethylpiperidine-1,3-dicarboxylate in 15 ml dry tetrahydrofuran 0.49 g (3.7 mmol) Potassium trimethylsilanolate was added, and the reaction mixture was refluxed for 1 hour. Distilled water was added, and the reaction mixture was acidified to pH=4 with acetic acid. The obtained mixture was extracted with ethyl acetate. The combined organic layer was washed with distilled water, brine, dried over anhydrous sodium sulfate, filtered and concentrated in vacuo to yield 0.39 g (85%) of the title compound. GC-MS (EI) m/z 258.2 [MH+]
A solution of 4.27 g (25.8 mmol) ethyl 2-methylpyridine-3-carboxylate in 40 ml distilled water was hydrogenated at 10 bar in the presence of 0.3 g PtO2×H2O for 12 hours at RT. The mixture was filtered through Celite and concentrated in vacuo to yield 3.94 g (89%) of the title compound. GC-MS (EI) m/z 172.1 [MH+]
The above obtained ethyl cis-2-methylpiperidine-3-carboxylate was dissolved in 20 ml distilled water and 40 ml tetrahydrofuran. 2.00 g (23.8 mmol) NaHCO3 and 5.00 g (22.9 mmol) BOC2O was added at 0° C. The reaction mixture was allowed to warm to RT, and stirred for 3 hours. 30 ml distilled water was added. The mixture was extracted with ethyl acetate. The combined organic layer was washed with distilled water, brine, dried over anhydrous sodium sulfate, filtered and concentrated in vacuo to yield 3.57 g (57%) of the title compound. GC-MS (EI) m/z 272.2 [MH+]
The above obtained 1-tert-butyl 3-ethyl cis-2-methylpiperidine-1,3-dicarboxylate was dissolved in 50 ml ethanol. 10 ml 6 M aqueous sodium hydroxide (60 mmol) was added dropwise at 0° C. The obtained mixture was allowed to warm to RT and stirred at this temperature for 18 hours. The reaction mixture was acidified to pH=3 with 1M HCl solution, and ethanol was evaporated. The mixture was extracted with ethyl acetate. The combined organic layer was washed with distilled water, brine, dried over anhydrous sodium sulfate, filtered and concentrated in vacuo to yield 2.81 g (88%) of the title compound. GC-MS (EI) m/z 244.1 [MH+]
Under nitrogen to a solution of 23.00 g (160.63 mmol) ethyl cis-2-methylpiperidine-3-carboxylate (Intermediate 22a) in 50 ml ethanol was added 2.00 g (87 mmol) sodium dissolved in 50 ml ethanol. The reaction mixture was refluxed for 16 hours. The mixture is concentrated in vacuo to obtain the title compound as an oil. The crude product is used in the next step.
The above obtained ethyl 2-methylpiperidine-3-carboxylate was dissolved in 200 ml tetrahydrofuran and 200 ml distilled water and 13.00 g (60 mmol) BOC2O was added. The reaction mixture was stirred for 16 hours at RT. The reaction mixture was acidified to pH=3 with 1M HCl solution and extracted with ethyl acetate. The combined organic layer was washed with distilled water, brine, dried over anhydrous sodium sulfate, filtered and concentrated in vacuo. The residue was chromatographed on silica gel eluting with 33% ethyl acetate in cyclohexane, then again with dichloromethane to yield 2.3 g (16%) of the title compound.
The title compound is prepared from 1-tert-butyl 3-ethyl 2-methylpiperidine-1,3-dicarboxylate according to the method described in Intermediate 22c.
The title compound is prepared from methyl (3S,4R)-4-methylpiperidine-3-carboxylate (prepared as described in US2010/0093706) according to the method described in Intermediate 22b.
The title compound is prepared from methyl 1-tert-butyl 3-methyl (3S,4R)-4-methylpiperidine-1,3-dicarboxylate according to the method described in Intermediate 22c.
The title compound is prepared from methyl (3R,4S)-4-methylpiperidine-3-carboxylate (prepared as described in US2010/0093706) according to the method described in Intermediate 22b.
The title compound is prepared from methyl 1-tert-butyl 3-methyl (3R,4S)-4-methylpiperidine-1,3-dicarboxylate according to the method described in Intermediate 22c.
A solution of 1.00 g (7.3 mmol) 5-methylpyridine-3-carboxylic acid in 20 ml acetic acid was hydrogenated at 10 bar in the presence of 0.2 g PtO2×H2O for 12 hours at RT. The mixture was filtered through Celite and concentrated in vacuo to yield 1.00 g (96%) of the title compound.
GC-MS (EI) m/z 144.1 [MH+]
The above obtained cis-5-methylpiperidine-3-carboxylic acid was dissolved in 10 ml distilled water and 10 ml tetrahydrofuran. 1.52 g (7 mmol) BOC2O was added at 0° C. The reaction mixture was allowed to warm to RT, and stirred for 3 hours. 30 ml distilled water was added. The mixture was extracted with ethyl acetate. The combined organic layer was washed with distilled water, brine, dried over anhydrous sodium sulfate, filtered and concentrated in vacuo to yield 0.45 g (25%) of the title compound. GC-MS (EI) m/z 244.1 [MH]
The title compound is prepared from 1-tert-butyl 3-ethyl piperidine-1,3-dicarboxylate and paraformaldehyde according to the method described in Intermediate 14a.
Under nitrogen, to a stirred solution of 0.296 g (1.03 mmol) ethyl 3-(hydroxymethyl) piperidine-3-carboxylate and 0.120 ml (1.48 mmol) pyridine in 5 ml of dichloromethane 0.230 ml (1.48 mmol) trifluoromethanesulfonic anhydride was added dropwise at (−78) ° C.—(−65) ° C. After addition the mixture was stirred at −78° C. for 5 min and allowed to warm to room temperature and stirred at this temperature for 18 h. The reaction mixture was quenched by addition of 1M hydrochloric acid solution. The reaction mixture was extracted with dichloromethane, the combined organic layer was washed with distilled water, dried over anhydrous sodium sulfate, filtered and concentrated in vacuo to obtain the title compound as oil. The crude product is used in the next step.
The above obtained 1-tert-butyl 3-ethyl 3-{[(1,1,2-trifluoroethanesulfonyl)oxy]methyl}piperidine-1,3-dicarboxylate was solved in 4 ml tetrahydrofuran and 1.25 ml (1.25 mmol) 1M tetrabutylammonium fluoride in tetrahydrofuran was added. The reaction mixture was stirred for 1 h at room temperature, diluted with water and extracted with ethyl acetate. The combined organic layer was washed with distilled water, dried over anhydrous sodium sulfate, filtered and concentrated in vacuo. The residue was chromatographed on silica gel eluting with 33% ethyl acetate in cyclohexane to yield 0.121 g (40%) of the title compound.
The title compound is prepared from 1-tert-Butyl 3-ethyl 3-(fluoromethyl)piperidine-1,3-dicarboxylate according to the method described in Intermediate 22c.
To a solution of 5.00 g (21.8 mmol) 1-[(tert-butoxy)carbonyl]piperidine-3-carboxylic acid in 30 ml dry tetrahydrofuran 3.89 g (24 mmol) CDI was added at 0° C., and the reaction mixture was allowed to warm to RT and stirred for 2 hours. In a separate flask, under nitrogen, to a solution of 24 ml 2 M lithium diisopropylamide in tetrahydrofuran/heptane/ethylbenzene (48 mmol) in 30 ml dry tetrahydrofuran, 3.2 ml (43.6 mmol) acetone was added dropwise at (−78) ° C.—(−65°) C. After addition the mixture was stirred at −78° C. for 1 hour, and the solution of the activated acid was added dropwise at (−78) ° C.-(−65) ° C. After addition, the mixture was stirred at −78° C. for 10 minutes, and quenched by the addition of 10% citric acid. The mixture was extracted with ethyl acetate. The combined organic layer was washed with distilled water, brine, dried over anhydrous sodium sulfate, filtered and concentrated in vacuo. The crude product was purified by silica gel chromatography eluting with dichloromethane to yield 2.28 g (39%) of the title compound. GC-MS (EI) m/z 270.2 [MH]
Compounds of Table 3 were prepared from the appropriate carboxylic acid and acetone according to the method described in Intermediate 28.
To a solution of 0.80 g (2.97 mmol) tert-butyl (3R)-3-(3-oxobutanoyl)piperidine-1-carboxylate (Intermediate 29) in 20 ml acetone was added 0.56 ml (8.91 mmol) iodomethane and 1.23 g (8.91 mmol) K2CO3. The reaction mixture was refluxed for 3 hours. The reaction mixture was allowed to cool to RT, acetone was evaporated, and the residue was partitioned between distilled water and ethyl acetate. The mixture was extracted with ethyl acetate. The combined organic layer was washed with distilled water, brine, dried over anhydrous sodium sulfate, filtered and concentrated in vacuo to yield 0.70 g (83%) of the title compound. GC-MS (EI) m/z 284.2 [MH+]
Compounds of Table 4 were prepared from the appropriate diketone and iodoalkane according to the method described in Intermediate 47.
Under nitrogen to a solution of 1.00 g (4.32 mmol) (2R)-4-[(tert-butoxy)carbonyl]morpholine-2-carboxylic acid in 10 ml dimethylformamide was added 1.27 g (13 mmol) N,O-Dimethylhydroxylamine hydrochloride, 3.77 ml (21.6 mmol) N,N-Diisopropylethyl amine, 1.8 g (4.76 mmol) HBTU, 0.73 g (4.76 mmol) HOBt*H2O at 0° C. The reaction mixture was allowed to warm to RT and stirred for 16 hours. Distilled water was added, and the mixture was extracted with ethyl acetate. The combined organic layer was washed with 1M HCl solution, 1M NaOH solution, distilled water, brine, dried over anhydrous sodium sulfate, filtered and concentrated in vacuo to yield 1.00 g (84%) of the title compound. GC-MS (EI) m/z 275.2 [MH+]
Under nitrogen the above obtained tert-butyl (2R)-2-[methoxy(methyl)carbamoyl]morpholine-4-carboxylate was dissolved in 20 ml dry tetrahydrofuran, and 11 ml 0.5 M 1-Propynyl magnesium bromide in tetrahydrofuran (5.5 mmol) was added dropwise at 0° C. The reaction mixture was stirred for 20 minutes at 0° C., and quenched by the addition of 10 ml saturated NH4Cl solution and 5 ml distilled water. The mixture was extracted with ethyl acetate. The combined organic layer was washed with distilled water, brine, dried over anhydrous sodium sulfate, filtered and concentrated in vacuo to yield 0.83 g (90%) of the title compound. GC-MS (EI) m/z 254.1 [MH+]
Compounds of Table 5 were prepared from the appropriate Weinreb amide and 1-Propynyl magnesium bromide according to the method described in Intermediate 63.
To a solution of 10 g (51 mmol) trans 4-(trifluoromethyl)cyclohexane-1-carboxylic acid in 150 ml methanol 10 ml (137 mmol) thionyl chloride was added dropwise at −10° C. After addition the mixture was allowed to warm to room temperature and stirred at this temperature for 16 h, then concentrated in vacuo. The residue was partitioned between ethyl acetate and water. The combined organic layer was washed with NaHCO3 solution and water, dried over anhydrous sodium sulfate, filtered and concentrated in vacuo to yield 8.96 g (84%) of the title compound. GC-MS (EI) m/z 211.2 [MH+]
Under nitrogen to a mixture of 9.1 ml (174 mmol) acetonitrile in 260 ml dry tetrahydrofuran 51 ml 2.5 M n-butyllithium in n-hexane solution (127 mmol) was added dropwise at (−78) ° C.-(−65) ° C. After addition the mixture was stirred at −78° C. for 1 h, 8.96 g (42.6 mmol) methyl trans-4-(trifluoromethyl)cyclohexane-1-carboxylate was added dropwise. The so obtained mixture was allowed to warm to room temperature and stirred at this temperature for 1 h. The reaction mixture was quenched by addition of 150 mL of saturated ammonium chloride solution. The tetrahydrofuran was evaporated and the mixture was extracted with ethyl acetate. The combined organic layer was washed with water, dried over anhydrous sodium sulfate, filtered and concentrated in vacuo. The crude product is used in the next step.
The above obtained 3-oxo-3-[trans-4-(trifluoromethyl)cyclohexyl]propanenitrile was solved in 187 ml of ethanol and 4.4 ml (167 mmol) of hydrazine monohydrate was added. Under inert gas atmosphere, the reaction mixture was refluxed for 16 h. The solvent was removed in vacuo and dry toluene was evaporated from the residue several times to yield 11.15 g of the title compound. LC-MS (ESI) m/z 234.2 [MH]
A mixture of 5 g (25.5 mmol) trans 4-(trifluoromethyl)cyclohexane-1-carboxylic acid, 100 ml dichloromethane, 5 ml (68.5 mmol) thionyl chloride and 0.1 ml dimethylformamide was refluxed for 6 h. The reaction mixture was concentrated in vacuo and dry tetrahydrofuran was evaporated from the residue several times. The crude product is used in the next step.
Under inert gas atmosphere, to a solution of the above obtained trans-4-(trifluoromethyl) cyclohexane-1-carbonyl chloride and 1.5 ml (26.96 mmol) fluoroacetonitrile in 50 ml dry tetrahydrofuran 50 ml (50 mmol) 1M lithium bis(trimethylsilyl)amide was added dropwise at −78° C. After addition the mixture was stirred at −78° C. for 1 h, then the mixture was allowed to warm to room temperature and poured into 200 ml of water. The pH of the mixture was adjusted to 2 by the addition of 1M hydrochloric acid. The mixture was extracted with ethyl acetate, the combined organic layer was washed with water, dried over anhydrous sodium sulfate, filtered and concentrated in vacuo. The crude product is used in the next step.
The above obtained 2-fluoro-3-oxo-3-[trans-4-(trifluoromethyl)cyclohexyl]propanenitrile was dissolved in 65 ml of ethanol and 4.4 ml (77 mmol) of hydrazine monohydrate was added. Under inert gas atmosphere, the reaction mixture was refluxed for 16 h. The solvent was removed in vacuo to obtain the title compound as oil. LC-MS (ESI) m/z 252.2 [MH+]
The title compound is prepared from trans-4-methylcyclohexane-1-carboxylic acid according to the method described in Intermediate 82a.
The title compound is prepared from Methyl trans-4-methylcyclohexane-1-carboxylate according to the method described in Intermediate 82b.
The title compound is prepared from 3-Oxo-3-(trans-4-methylcyclohexyl)propanenitrile according to the method described in Intermediate 82c.
The title compound is prepared from trans-4-tert-butylcyclohexane-1-carboxylic acid according to the method described in Intermediate 82a.
The title compound is prepared from Methyl trans-4-tert-butylcyclohexane-1-carboxylate according to the method described in Intermediate 82b.
The title compound is prepared from 3-Oxo-3-(trans-4-tert-butylcyclohexyl)propanenitrile according to the method described in Intermediate 82c.
The title compound is prepared as described in WO2018/167629.
To a solution 0.50 g (2.14 mmol) 3-[trans-4-(Trifluoromethyl)cyclohexyl]-1H-pyrazol-5-amine (Intermediate 82) in 30 ml toluene was added 0.30 ml (2.37 mmol) ethyl acetoacetate and a catalytic amount of p-Toluenesulfonic acid monohydrate. The reaction mixture was refluxed for 16 hours, and allowed to warm to RT. The precipitated crystals were filtered to yield 0.51 g (79%) of the title compound. LC-MS (ESI) m/z 300.1 [MH+]
The above obtained 5-methyl-2-[trans-4-(trifluoromethyl)cyclohexyl]pyrazolo[1,5-a]pyrimidin-7-ol was suspended in 10 ml toluene, 0.59 ml (3.40 mmol) N,N-Diisopropylethylamine and 0.80 ml (8.50 mmol) phosphoryl chloride was added. The reaction mixture was refluxed for 2 hours and then quenched the by the addition of ice. The reaction mixture was neutralized by the addition of saturated NaHCO3 solution. The resulting mixture was extracted with ethyl acetate. The combined organic layer was washed with distilled water, dried over anhydrous sodium sulfate, filtered and concentrated in vacuo to yield 0.53 g (99%) of the title compound. LC-MS (ESI) m/z 318.1 [MH+]
To a solution of 0.81 g (3 mmol) tert-butyl 3-(3-oxobutanoyl)piperidine-1-carboxylate (Intermediate 28) in 25 ml toluene was added 0.50 g (2.14 mmol) 3-[trans-4-(Trifluoromethyl)cyclohexyl]-1H-pyrazol-5-amine (Intermediate 82) and 0.02 g (0.1 mmol) p-Toluenesulfonic acid monohydrate. The reaction mixture was refluxed for 16 hours and the solvent was evaporated. The residue was purified by silica gel chromatography eluting with 0-30% ethyl acetate in cyclohexane to yield 0.26 g (26%) of the title compound. LC-MS (ESI) m/z 467.2 [MH]
To a solution of 0.83 g (3.28 mmol) tert-butyl (2R)-2-(but-2-ynoyl)morpholine-4-carboxylate (Intermediate 63) in 10 ml ethanol was added 0.27 ml (3.28 mmol) pyrrolidine. The reaction mixture was stirred at RT for 30 minutes and 0.77 g (3.28 mmol) 3-[trans-4-(Trifluoromethyl)cyclohexyl]-1H-pyrazol-5-amine (Intermediate 82) and 1.5 ml acetic acid was added. The reaction mixture was stirred at 60° C. for 4 hours, and the solvent was evaporated. The residue was purified by silica gel chromatography eluting with 0-50% ethyl acetate in cyclohexane to yield 1.45 g (95%) of the title compound. LC-MS (ESI) m/z 469.2 [MH]
To a solution of 1.12 g (4.75 mmol) tert-butyl 1,1-dioxo-1λ6-thiomorpholine-4-carboxylate (prepared as described in EP1140904) in 30 ml dry tetrahydrofuran 4.8 mL 1 M lithium bis(trimethylsilyl)amide in tetrahydrofuran solution (4.8 mmol) was added dropwise at (−78) ° C.-(−65) ° C. After addition the mixture was stirred at −78° C. for 1 hour, 1.26 g (3.96 mmol) 7-chloro-5-methyl-2-[trans-4-(trifluoromethyl)cyclohexyl]pyrazolo[1,5-a]pyrimidine (Intermediate 87) was added. The so obtained mixture was allowed to warm to RT and stirred at this temperature for 18 h. The reaction mixture was quenched by addition of 20 ml saturated ammonium chloride solution and 10 ml distilled water. The reaction mixture was extracted with ethyl acetate, the combined organic layer was washed with distilled water, brine, dried over anhydrous sodium sulfate, filtered and concentrated in vacuo. The residue was purified by silica gel chromatography eluting with 0-35% ethyl acetate in cyclohexane to yield 0.63 g (31%) of the title compound. LC-MS (ESI) m/z 517.2 [MH+]
Intermediates 91-155 were prepared using analogues methods to those Intermediates described above and are exemplified below in Table 6.
To a solution of 1.00 g (2.14 mmol) tert-butyl 3-{5-methyl-2-[trans-4-(trifluoromethyl)cyclohexyl]pyrazolo[1,5-a]pyrimidin-7-yl}piperidine-1-carboxylate (Intermediate 88) in 20 ml dichloromethane was added 3.3 ml (42.8 mmol) trifluoroacetic acid dropwise at 0° C. The reaction mixture was allowed to warm to RT and stirred for 16 hours. 10 ml distilled water was added, and the pH was adjusted to 10 by the addition of 2 M aqueous sodium hydroxide. The mixture was extracted with dichloromethane. The combined organic layer was washed with distilled water, brine, dried over anhydrous sodium sulfate, filtered and concentrated in vacuo to yield 0.70 g (89%) of the title compound. LC-MS (ESI) m/z 367.2 [MH+]
Intermediates 157-221 were prepared using analogues methods to those Intermediates described above and are exemplified below in Table 7.
To a solution of 0.07 g (0.18 mmol) (3R)-3-methyl-3-{5-methyl-2-[trans-4-(trifluoromethyl)cyclohexyl]pyrazolo[1,5-a]pyrimidin-7-yl}piperidine (Intermediate 167) in 2 ml toluene was added 0.03 ml (0.28 mmol) methyl bromoacetate and 0.1 ml (0.57 mmol) N,N-Diisopropylethylamine. The reaction mixture was stirred for 16 hours at RT and diluted with toluene. The mixture was washed with distilled water, brine, dried over anhydrous sodium sulfate, filtered and concentrated in vacuo. The crude product was purified by silica gel chromatography eluting with 5% acetone in dichloromethane to yield 0.06 g (80%) of the title compound. LC-MS (ESI) m/z 453.2 [MH+]
Under nitrogen to a solution of 0.17 g (0.45 mmol) (3R)-3-{5,6-dimethyl-2-[trans-4-(trifluoromethyl)cyclohexyl]pyrazolo[1,5-a]pyrimidin-7-yl}piperidine (Intermediate 158) in 10 ml dimethylformamide was added 0.09 g (0.46 mmol) Boc-Ser-OH, 0.08 g (0.54 mmol) 1-Hydroxybenzotriazole hydrate, 0.2 ml (1.12 mmol) N,N-Diisopropylethylamine and 0.1 g (0.54 mmol) EDC at 0° C. The reaction mixture was allowed to warm to RT, and stirred for 16 hours. The reaction mixture was diluted with distilled water. The resulting mixture was extracted with ethyl acetate. The combined organic layer was washed with distilled water, dried over anhydrous sodium sulfate, filtered and concentrated in vacuo. The residue was purified by silica gel chromatography eluting with 4% methanol in dichloromethane to yield 0.12 g (46%) of the title compound. LC-MS (ESI) m/z 568.3 [MH+]
Intermediates 225-226 were prepared using analogues methods to those Intermediates described above and are exemplified below in Table 8.
To a solution of 0.18 g (0.47 mmol) 3-{5-methyl-2-[trans-4-(trifluoromethyl)cyclohexyl]pyrazolo[1,5-a]pyrimidin-7-yl}piperidine (Intermediate 156) in 15 ml dichloromethane was added 0.1 ml (0.7 mmol) triethylamine and 0.04 ml (0.56 mmol) acetyl chloride. The reaction mixture was stirred for 2 hours at RT and washed with distilled water, dried over anhydrous sodium sulfate, filtered and concentrated in vacuo. The crude product was purified by silica gel chromatography eluting with 0-10% methanol in dichloromethane to yield 0.17 g (85%) of the title compound. LC-MS (ESI) m/z 409.2 [MH+]
The racemic form of the title compounds (Example 158) were prepared from cis-3-{3-fluoro-5-methyl-2-[trans-4-(trifluoromethyl)cyclohexyl]pyrazolo[1,5-a]pyrimidin-7-yl}-4-methylpiperidine (Intermediate 159) according to the method described in Example 1. LC-MS (ESI) m/z 441.2 [MH+]. The A and B enantiomers were separated using chiral preparative HPLC (Lux i-Amylose-1 5 μm 250×21.2 mm; F=21.34 ml/min; eluents: A: n-heptane B: 2-propanol; isocratic 5% B t=25° C.) obtaining enantiomer A (Tr 13.625, Example 2), and enantiomer B (Tr 20.089, Example 3). Their absolute configuration is not determined.
The racemic form of the title compounds (Example 159) were prepared from trans-4-methyl-3-{5-methyl-2-[trans-4-(trifluoromethyl)cyclohexyl]pyrazolo[1,5-a]pyrimidin-7-yl}piperidine (Intermediate 171) and methyl chloroformate according to the method described in Example 1. LC-MS (ESI) m/z 439.2 [MH]. The A and B enantiomers were separated using chiral preparative HPLC (Lux i-Amylose-1 5 μm 150×21.1 mm; F=10 ml/min; eluents: A: water B: 2-propanol; isocratic 55% B t=40° C.) obtaining enantiomer A (Tr 18.886, Example 4), and enantiomer B (Tr 24.444, Example 5). Their absolute configuration was determined with VCD spectroscopy. Example 4 is (3R,4S) and Example 5 is (3S,4R).
The racemic form of the title compounds (Example 76) were prepared from cis-4-methyl-3-{5-methyl-2-[trans-4-(trifluoromethyl)cyclohexyl]pyrazolo[1,5-a]pyrimidin-7-yl}piperidine (Intermediate 180) and methyl chloroformate according to the method described in Example 1. LC-MS (ESI) m/z 439.2 [MH+]. The A and B enantiomers were separated using chiral preparative HPLC (Lux i-Amylose-1 5 μm 150×21.1 mm; F=10 ml/min; eluents: A: water B: 2-propanol; isocratic 55% B t=40° C.) obtaining enantiomer A (Tr 18.886, Example 6), and enantiomer B (Tr29.748, Example 7). Their absolute configuration is not determined.
The racemic form of the title compounds (Example 160) were prepared from cis-4-methyl-3-{5-methyl-2-[trans-4-(trifluoromethyl)cyclohexyl]pyrazolo[1,5-a]pyrimidin-7-yl}piperidine (Intermediate 180) and formic acid according to the method described in Example 22. LC-MS (ESI) m/z 409.2 [MH]. The A and B enantiomers were separated using chiral preparative HPLC (Chiral Pak IG 20 μm 200×50 mm; F=50 ml/min; eluents: A: n-heptane B: dichloromethane; isocratic 50% B t=25° C.) obtaining enantiomer A (Tr 27, Example 8), and enantiomer B (Tr 51, Example 9). Their absolute configuration is not determined.
The enantiomerically enriched form of the title compounds were prepared from (2S)-5,5-dimethyl-2-{5-methyl-2-[trans-4-(trifluoromethyl)cyclohexyl]pyrazolo[1,5-a]pyrimidin-7-yl}morpholine or (2R)-5,5-dimethyl-2-{5-methyl-2-[trans-4-(trifluoromethyl)cyclohexyl]pyrazolo[1,5-a]pyrimidin-7-yl}morpholine (Intermediate 200 or Intermediate 201) and formic acid according to the method described in Example 22. LC-MS (ESI) m/z 425.2 [MH+]. The A and B enantiomers were separated using chiral preparative HPLC (Reprosil Chiral MIX 5 μm 150×20 mm; F=20 ml/min; eluents: A: water B: acetonitrile; isocratic 50% B t=40° C.) obtaining enantiomer A (Tr 12.783, Example 10), and enantiomer B (Tr 15.088, Example 11).
The enantiomerically enriched form of the title compound were prepared from (2S)-5,5-dimethyl-2-{5-methyl-2-[trans-4-(trifluoromethyl)cyclohexyl]pyrazolo[1,5-a]pyrimidin-7-yl}morpholine (Intermediate 200) and methyl chloroformate according to the method described in Example 1. LC-MS (ESI) m/z 455.2 [MH+]. The A and B enantiomers were separated using chiral preparative HPLC (Lux Cellulose-3 5 μm 250×21.1 mm; F=20 ml/min; eluents: A: n-heptane B: 2-propanol; isocratic 10% B t=40° C.) obtaining enantiomer A (Tr 4.788, Example 12).
The racemic form of the title compounds were prepared from 1-{5-methyl-2-[trans-4-(trifluoromethyl)cyclohexyl]pyrazolo[1,5-a]pyrimidin-7-yl}-3-azabicyclo[4.1.0]heptane (Intermediate 206) and methyl chloroformate according to the method described in Example 1. LC-MS (ESI) m/z 437.2 [MH+]. The A and B enantiomers were separated using chiral preparative HPLC (Lux Cellulose-3 5 μm 250×21.2 mm; F=25 ml/min; eluents: A: water B: acetonitrile; isocratic 50% B t=40° C.) obtaining enantiomer A (Tr 6.811, Example 13), and enantiomer B (Tr 7.479, Example 14). Their absolute configuration is not determined.
The racemic form of the title compounds were prepared from 1-{3-fluoro-5-methyl-2-[trans-4-(trifluoromethyl)cyclohexyl]pyrazolo[1,5-a]pyrimidin-7-yl}-3-azabicyclo[4.1.0]heptane (Intermediate 207) and methyl chloroformate according to the method described in Example 1. LC-MS (ESI) m/z 455.2 [MH+]. The A and B enantiomers were separated using chiral preparative HPLC (Lux Cellulose-3 5 μm 250×21.2 mm; F=25 ml/min; eluents: A: water B: acetonitrile; isocratic 50% B t=40° C.) obtaining enantiomer A (Tr 8.811, Example 15), and enantiomer B (Tr 10.414, Example 16). Their absolute configuration is not determined.
To a solution of 0.16 g (0.73 mmol) Sodium periodate in 10 ml distilled water was added 0.1 g (0.23 mmol) methyl 2-{5-methyl-2-[trans-4-(trifluoromethyl)cyclohexyl]pyrazolo[1,5-a]pyrimidin-7-yl}thiomorpholine-4-carboxylate (Example 126), 10 ml methanol and 10 ml dioxane at 0° C. The reaction mixture was allowed to warm to RT and stirred for 16 hours. The organic solvents were evaporated, and the mixture was filtered to yield 0.07 g (66%) of the title compound. LC-MS (ESI) m/z 459.2 [MH+]
The title compound is prepared from (3R)-3-{5,6-dimethyl-2-[trans-4-(trifluoromethyl)cyclohexyl]pyrazolo[1,5-a]pyrimidin-7-yl}-3-methylpiperidine (Intermediate 170) and bromoacetonitrile according to the method described in Intermediate 224.
To a solution of 0.05 g (0.12 mmol) 2-[(3R)-3-{5,6-dimethyl-2-[trans-4-(trifluoromethyl)cyclohexyl]pyrazolo[1,5-a]pyrimidin-7-yl}-3-methylpiperidin-1-yl]acetonitrile in 5 ml diethyl ether was added 1 ml hydrochloric acid in ethyl acetate was added. The precipitate was filtered to yield 0.04 g (67%) of the title compound. LC-MS (ESI) m/z 434.3 [MH].
To a suspension of 0.06 g methyl 2-[(3R)-3-methyl-3-{5-methyl-2-[trans-4-(trifluoromethyl)cyclohexyl]pyrazolo[1,5-a]pyrimidin-7-yl}piperidin-1-yl]acetate (Intermediate 224) in 0.5 ml distilled water was added 0.5 ml 37% hydrochloric acid. The mixture was refluxed for 16 hours. The reaction mixture was concentrated in vacuo, and triturated with diethyl ether. The mixture was filtered to yield 0.04 g (73%) of the title compound. LC-MS (ESI) m/z 439.2 [MH+].
Under nitrogen to a solution of 0.08 g (0.19 mmol) 5-{5,6-dimethyl-2-[-4-(trifluoromethyl)cyclohexyl]pyrazolo[1,5-a]pyrimidin-7-yl}-3,3-difluoropiperidine (Intermediate 179) in 1 ml dimethylformamide was added 0.03 g (0.23 mmol) 3-Methyloxetane-3-carboxylic acid, 0.07 g (0.19 mmol) HBTU and 0.11 ml (0.634 mmol) N,N-Diisopropylethylamine. The reaction mixture was stirred for 16 hours. The reaction mixture was diluted with distilled water. The resulting mixture was extracted with ethyl acetate. The combined organic layer was washed with distilled water, dried over anhydrous sodium sulfate, filtered and concentrated in vacuo. The residue was purified by silica gel chromatography eluting with 5% methanol in dichloromethane to yield 0.05 g (50%) of the title compound. LC-MS (ESI) m/z 515.2 [MH+]
To a solution of 0.12 g (0.21 mmol) tert-butyl N-[(2S)-1-[(3R)-3-{5,6-dimethyl-2-[trans-4-(trifluoromethyl)cyclohexyl]pyrazolo[1,5-a]pyrimidin-7-yl}piperidin-1-yl]-3-hydroxy-1-oxopropan-2-yl]carbamate (Intermediate 225) in 5 ml dichloromethane was added 1 ml (10 mmol) trifluoroacetic acid. The reaction mixture was stirred at RT for 16 hours and the pH was adjusted to 8 by the addition of saturated NaHCO3 solution. The mixture was extracted with dichloromethane. The combined organic layer was washed with distilled water, brine, dried over anhydrous sodium sulfate, filtered and concentrated in vacuo. The residue was purified by silica gel chromatography eluting with 10% methanol in dichloromethane to yield 0.04 g (43%) of the title compound. LC-MS (ESI) m/z 468.2 [MH+]
To a solution of 0.16 g (0.45 mmol) (3R)-3-{5-methyl-2-[trans-4-(trifluoromethyl)cyclohexyl]pyrazolo[1,5-a]pyrimidin-7-yl}piperidine (Intermediate 157) in 10 ml toluene was added 0.2 ml (53.4 mmol) formic acid. The reaction mixture was refluxed for 3 hours and evaporated. The crude product was purified by silica gel chromatography eluting with 0-100% ethyl acetate in cyclohexane to yield 0.14 g (78%) of the title compound. LC-MS (ESI) m/z 395.2 [MH+]
To a solution of 0.08 g (0.2 mmol) (3R)-3-{5-methyl-2-[trans-4-(trifluoromethyl)cyclohexyl]pyrazolo[1,5-a]pyrimidin-7-yl}piperidine (Intermediate 157) in 1 ml dimethylformamide was added 0.06 g (0.4 mmol) 1-Amidinopyrazole Hydrochloride and 0.07 ml (0.4 mmol) N,N-Diisopropylethylamine. The reaction mixture was stirred for 16 hours at RT and filtered to yield 0.09 g (97%) of the title compound. LC-MS (ESI) m/z 409.3 [MH]
To a solution of 0.13 g (0.34 mmol) (3R)-3-{5-methyl-2-[trans-4-(trifluoromethyl)cyclohexyl]pyrazolo[1,5-a]pyrimidin-7-yl}piperidine (Intermediate 157) in 5 ml 1,2-dichloroethane was added 0.03 ml (0.34 mmol) acetone, 0.1 g (0.48 mmol) Sodium triacetoxyborohydride and 0.02 ml (0.34 mmol) acetic acid. The reaction mixture was stirred for 16 hours at RT and washed with 1M NaOH solution. The organic layer was washed with distilled water, brine, dried over anhydrous sodium sulfate, filtered and concentrated in vacuo. The crude product was purified by silica gel chromatography eluting with 0-10% methanol in dichloromethane to yield 0.05 g (38%) of the title compound. LC-MS (ESI) m/z 409.3 [MH+]
To a solution of 0.12 g (0.33 mmol) (2R)-2-{5-methyl-2-[trans-4-(trifluoromethyl)cyclohexyl]pyrazolo[1,5-a]pyrimidin-7-yl}morpholine (Intermediate 222) in 15 ml dioxane was added 0.31 g (3.23 mmol) sulfamide. The reaction mixture was refluxed for 1 hour and evaporated. The crude product was purified by silica gel chromatography eluting with 0-100% ethyl acetate in cyclohexane to yield 0.03 g (21%) of the title compound. LC-MS (ESI) m/z 448.2 [MH+]
To a solution of 0.12 g (0.33 mmol) (2R)-2-{5-methyl-2-[trans-4-(trifluoromethyl)cyclohexyl]pyrazolo[1,5-a]pyrimidin-7-yl}morpholine (Intermediate 222) in 10 ml dichloromethane was added 0.1 ml (0.72 mmol) (Trimethylsilyl)isocyanate. The reaction mixture was stirred for 3 hours at RT. The reaction mixture was washed with distilled water, brine, dried over anhydrous sodium sulfate, filtered and concentrated in vacuo. The crude product was purified by silica gel chromatography eluting with 0-10% methanol in dichloromethane to yield 0.06 g (48%) of the title compound. LC-MS (ESI) m/z 412.2 [MH+]
The title compound is prepared from 3-[trans-4-(trifluoromethyl)cyclohexyl]-1H-pyrazol-5-amine (Intermediate 82) and 3-(but-2-ynoyl)-1λ6-thiane-1,1-dione (Intermediate 73) according to the method described in Intermediate 89. LC-MS (ESI) m/z 416.2 [MH+]
The racemic form of the title compounds (Example 161) were prepared from 3-[trans-4-(trifluoromethyl)cyclohexyl]-1H-pyrazol-5-amine (Intermediate 82) and 1-(oxan-3-yl)butane-1,3-dione (Intermediate 45) according to the method described in Intermediate 88. LC-MS (ESI) m/z 368.2 [MH]. The A and B enantiomers were separated using chiral preparative HPLC (Lux i-Amylose-1 5 μm 150×21.1 mm; F=20 ml/min; eluents: A: water B: acetonitrile; isocratic 50% B t=40° C.) obtaining enantiomer A (Tr 26.148, Example 28), and enantiomer B (Tr 30.798, Example 29).
The title compound is prepared from 7-chloro-5-methyl-2-[trans-4-(trifluoromethyl)cyclohexyl]pyrazolo[1,5-a]pyrimidine (Intermediate 87) and 4-methylmorpholin-3-one according to the method described in Intermediate 90. LC-MS (ESI) m/z 397.2 [MH+]
To a solution of 0.39 g (2.42 mmol) Carbonyldiimidazole in 20 ml dichloromethane was added 0.1 ml (2.42 mmol) CD3OD at 0° C. The reaction mixture was stirred for 1 hours at RT. To this mixture, 0.89 g (2.42 mmol) (2S)-2-{5-methyl-2-[trans-4-(trifluoromethyl)cyclohexyl]pyrazolo[1,5-a]pyrimidin-7-yl}morpholine (Intermediate 187) dissolved in 10 ml dichloromethane was added. The reaction mixture was stirred at RT for 16 hours. The reaction mixture was washed with distilled water, brine, dried over anhydrous sodium sulfate, filtered and concentrated in vacuo. The crude product was purified by silica gel chromatography eluting with 0-10% methanol in dichloromethane to yield 0.09 g (8%) of the title compound. LC-MS (ESI) m/z 430.4 [MH+]
Examples 32-161 were prepared using analogues methods to those Examples described above and are exemplified below in Table 9.
The following formulation examples illustrate representative pharmaceutical compositions of this invention. The present invention however is not limited to the following pharmaceutical compositions.
I. Tablets
II. Orodispersible Films
III. Oral Suspensions
IV. Syrups
V. Intravenous Injections
VI. Suppositories
VII. Eye Drops
| Number | Date | Country | Kind |
|---|---|---|---|
| P2000254 | Aug 2020 | HU | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/IB2021/057180 | 8/5/2021 | WO |
