Patent Application
20130012522
This invention concerns a series derived from N-methyl-N-{[(1-methyl-5-alcoxy)-1H-indol-2-yl]methyl}prop-2-yn-1-amine, that are multipotent inhibitors of monoamine oxidase A and B enzymes, acetylcholinesterase and butyrylcholinesterase, with possible application within the pharmaceutical industry field as medications to cure, delay, or alleviate neurodegenerative diseases such as Alzheimer's disease and Parkinson's disease.
Alzheimer's disease (AD), the most common dementia in older people, is a complex neurodegenerative disorder of the central nervous system, characterized by a progressive loss of intellectual abilities (memory, language, and reasoning) and psychiatric disorders (apathy, anxiety, depression, aggression). Although its etiology is not fully understood, there are several characteristics of the disease which play an important role in this pathology, as senile plaques (β-amyloid deposits derived from abnormal metabolism of the amyloid precursor protein), neurofibrillary tangles (comprised of abnormally hyperphosphorylated tau protein), oxidative damage to various cellular structures and low levels of the neurotransmitter acetylcholine.
Current treatments are fundamentally symptomatic. In recent decades, the cholinergic approach has placed four drugs on the market for treatment of the disease: acetylcholinesterase enzyme inhibitors (AChE) tacrine, donepezil, rivastigmine, and galantamine, which enhance neurotransmission in the cholinergic synapses of the brain, alleviating cognitive deficits (Villarroya, M. et al., Expert Opin. Investig. Drugs 2007, 16, 1987-1998). So far, the only drug approved of a noncholinergic nature is memantine, an N-methyl-D-aspartate antagonist, which increases memory and intellectual abilities by modulation of the glutamatergic system (Parsons, C. G. et al., Neuropharmacology 2007, 53, 699-723). Below are approved drugs for the treatment of AD:
The AChE enzyme has two major sites: the active catalytic center (CAS) where hydrolysis of acetylcholine is produced and where the bottom of a narrow throat is found and the peripheral anionic site (PAS) located in the catalytic throat inlet.
Apart from its role in cholinergic transmission, AChE has other functions related to neuronal differentiation, cell adhesion, and aggregation of the amyloid peptide. Different biochemical studies have revealed that AChE promotes the formation of aggregates of β-amyloid (An), establishing AChE-Aβ complexes which are more toxic than the isolated Aβ itself. Since the point of attachment between the enzyme and the peptide is located on the PAS, the dual AChE inhibitors, capable of interacting simultaneously with CAS and PAS sites are of great interest in AD since they can ameliorate cognitive deficits and halt related the neurotoxicity of Aβ (Ferrari, G. V. et al., Biochemistry 2001, 40, 10447-10457). In recent years, various families of dual AChE inhibitors have been described (for example, Fernández-Bachiller, M. I. et al., ChemMedChem 2009, 4, 828-841; Muñoz-Torrero, D., Curr. Med. Chem. 2008, 15, 2433-2455).
The inhibition of monoamine oxidases has an interesting pharmacological property to be taken into account when designing new drugs for potential treatment of AD and Parkinson's, since during the deamination reaction of the neurotransmitter amines, such as adrenaline, dopamine and serotonin, catalyzed by MAOs, hydrogen peroxide is generated (H2O2), which is a source of oxygenated free radicals, highly toxic agents, and responsible for the oxidative stress that negatively affects the neurons in AD and Parkinson's (Schneider, L. S. et al. Am. J. Psychiatry 1993, 18, 321-323; Marin, D. B. et al. Psychiatry Res. 1995, 58, 181-189; Alper, G. et al. Eur. Neuropsychopharmacol. 1999, 9, 247-252).
This invention concerns a series derived from N-methyl-N-{[(1-methyl-5-alcoxy)-1H-indol-2-yl]methyl}prop-2-yn-1-amine, that exhibit inhibitory activity of the monoamine oxidases A and B enzymes, acetylcholinesterase, and butyrylcholinesterase, involved in the biochemical processes related to the development of symptoms of some neurodegenerative diseases such as Alzheimer's disease or Parkinson's disease.
In a first aspect, this invention relates to a compound of formula (I)
where,
R1 and R2 are selected from H and C1-C10 alkyl,
R3 is selected from H, —OR4, N, —CN, —C(O)R4, —C(O)OR4, —C(O)NR4R5, —C═NR4, —OC(O)R4, —NR4R5, —NR4C(O)R5, —NO2, —N═CR4R5, halogen and C1-C10 alkyl,
where R4 and R5 are selected from H, alkyl, alkenyl, cycloalkyl and aryl,
X, Y, Z1, Z2 y Z3 are selected independently from CH and N,
A is selected from (CH2)n, NH, O and CO, where n is a whole number from 1 to 6, or their salts, isomers or solvates
The term “alkyl” refers to, in this invention, to linear or branched hydrocarbon chain radicals, having from 1 to 10 carbon atoms, preferably 1 to 4, and which bind to the rest of the molecule by a single bond, for example, methyl, ethyl, n-propyl, i-propyl, n-butyl, tert-butyl, sec-butyl, n-pentyl, n-hexyl, etc. The alkyl groups may be optionally substituted by one or more substituents such as halogen, hydroxyl, alkoxyl, carboxyl, carbonyl, cyano, acyl, alkoxycarbonyl, amino, nitro, mercapto, and alkylthio.
The term “alkenyl” refers to radicals of hydrocarbon chains containing one or more carbon-carbon double bonds, for example vinyl, 1-propenyl, allyl, isoprenyl, 2-butenyl, 1,3-butadienyl, etc. The alkyl radicals may be optionally substituted by one or more substituents such as halogen, hydroxyl, alkoxyl, carboxyl, cyano, carbonyl, acyl, alkoxycarbonyl, amino, nitro, mercapto, and alkylthio.
“Cycloalkyl” refers in this invention to a stable monocyclic or bicyclic radical of 3 to 10 members, which is saturated or partially saturated, and which consists only of carbon and hydrogen atoms, such as cyclopentyl, cyclohexyl or adamantyl, and which may be optionally substituted by one or more groups such as alkyl, halogen, hydroxyl, alkoxyl, carboxyl, cyano, carbonyl, acyl, alkoxycarbonyl, amino, nitro, mercapto and alkylthio.
The term “aryl” refers within this invention to a radical phenyl, naphthyl, indenyl, phenanthryl or anthracyl. The alkyl radical may be optionally substituted by one or more substituents such as alkyl, haloalkyl, aminoalkyl, dialkylamino, hydroxyl, alkoxy, phenyl, mercapto, halogen, nitro, cyano and alkoxycarbonyl.
In a preferred embodiment, where X and/or Y is CH.
In another preferred embodiment, R3 is H.
In another preferred embodiment, R1 y R2 are independently a C1-C4 alkyl.
In another aspect, this invention relates to a compound of formula (II):
where X and Y are independently selected from CH and N,
A is selected from (CH2)n, NH, O and CO, where n is a whole number from 1 to 6.
In a preferred embodiment, A is a (CH2)n group, where n is a whole number from 1 to 4.
In another preferred embodiment, X is N.
In another preferred embodiment, Y is N.
In another aspect, this invention refers to a compound that is selected from the following list:
An additional preferred embodiment refers to the following compounds:
The compounds of the present invention represented by the formula (I) may include isomers, depending on the presence of multiple bonds (for example Z, E), including optical isomers or enantiomers, depending on the presence of chiral centers. The individual isomers, enantiomers, or diastereoisomers and mixtures thereof fall within the scope of this invention, i.e., the isomer term also refers to any mixture of isomers, as diastereomers, racemates, etc., including their optically active isomers or mixtures in various proportions thereof. The individual enantiomers or diastereoisomers, as well as their mixtures, may be separated by conventional techniques.
In another aspect, this invention relates to a pharmaceutical composition comprising at least one compound of formula (I) as defined above and at least one adjuvant, excipient and/or pharmaceutically acceptable carrier. In another preferred embodiment, this composition further comprises another active ingredient.
For its application in therapy, the compounds of formula (I), salts or isomers thereof, will preferably be found in a pharmaceutically acceptable or substantially pure form, i.e., having a pharmaceutically acceptable level of purity excluding normal pharmaceutical additives such as diluents and carriers, and including no material considered toxic at normal dosage levels. The purity levels for the active ingredient are preferably above 50%, more preferably above 70%, and still more preferably above 90%. In a preferred embodiment, they are above 95% of the compound of formula (I).
The pharmaceutically acceptable adjuvants and carriers that may be used in said compositions are the adjuvants and carriers known by those skilled in the art and habitually used in the preparation of therapeutic compositions.
In another particular embodiment, said pharmaceutical composition is prepared in a solid form or an aqueous suspension, in a pharmaceutically acceptable diluent. The therapeutic composition provided by this invention can be administered via any appropriate route of administration, for which said composition will be formulated in the proper pharmaceutical form for the chosen route of administration. In a particular embodiment, administration of the therapeutic composition provided by this invention is carried out by oral, topical, rectal or parenteral (including subcutaneous, intraperitoneal, intradermal, intramuscular, intravenous, etc.) route.
In another aspect, this invention relates to the use of a compound of formula (I) as described above for the manufacture of a medication.
In another aspect, this invention relates to the use of a compound of formula (I) as described above for the manufacture of a medication for treatment of a neurodegenerative disease.
In a preferred embodiment, the neurodegenerative disease is selected from senile dementia, cerebrovascular dementia, mild cognitive impairment, attention deficit disorders, neurodegenerative diseases associated with aberrant protein aggregations as Parkinson's disease or Alzheimer's disease, amyotrophic lateral sclerosis, prion diseases such as Creutzfeldt-Jakob disease or Gerstmann-Straussler-Scheinker. In an even more preferred embodiment, the neurodegenerative disease is Parkinson's disease or Alzheimer's disease.
The use of the compounds of the invention is compatible with their use in protocols wherein the compounds of formula (I), or mixtures thereof are used by themselves or in combination with other treatments or medical procedures.
One aspect of the present invention relates to a method of obtaining a compound of formula (I) which comprises the reaction of a compound of formula (III)
where R1, R2 and A are as defined above,
with a compound of formula (IV):
where R3, X, Y and Z1, Z2 and Z3 are as defined above.
Another aspect of the present invention relates to a method of obtaining a compound of formula (I) which comprises the reaction of a compound of formula (V):
where R1, R2 are as defined above,
and a compound of formula (VI):
where R3, A, X, Y, Z1, Z2 and Z3 are as defined above.
Throughout the description and claims the word “comprise” and its variants do not intend to exclude other technical features, additives, components or steps. For those skilled in the art, other objects, advantages and features of the invention will emerge partly from the description and partly from the practice of the invention. The following examples and drawings are provided as a way to illustrate and are not intended to limit this invention.
The invention will be illustrated below by means of tests made by the inventors, which show the specificity and effectiveness of the compounds of formula (I) of the invention.
All the anhydrous solvents were distilled using a Pure sols solvent purification system model PS-400-3-MD. The melting points (not corrected), and measured on a Kofler-type microscope (Reichert Jung Thermovar). The 1H-NMR and 13C NMR spectra were performed on a Varian (nova-300 (300 MHz), Mercury-400 (400 MHz), Varian (nova-400 (400 MHz) and Unity-500 (500 MHz). Chemical shifts (in ppm) are referenced to the residual solvent signal used [CDCl3: 7.27 (D), 77.2 (C) ppm; CD3OD: 4.84 (d), 49.05 (C) ppm]. The multiplicity of signals (5, singlet; d, doublet; t, triplet; c: quartet, q, quintet, m, multiplet), number of protons (deducted by integration), the value of the coupling constants J (in hertz) and the structural assignment inferred from studying bidimensional experiments (1H, 1H-COSY, 1H, 13C-HSQC, 1H, 13C-HMBC). Mass spectra were recorded on an LC/MS HP-1100MSD spectrometer with APCI and API-ES ionization sources. Also, in the cases, the spectra were recorded by electron impact on a sample injection HP-5873MSD spectrometer by direct probe. Infrared spectra were obtained on a Perkin-Elmer Spectrum One on a KBr pellet. The most significant bands are indicated in cm−1. The elemental analyzes were performed with a Heraus CHN-O Rapid analyzer and are expressed in percentages. Chromatographic separations were performed by column chromatography using Merck silica gel 60 (0.063-0200 nm) under pressure (flash) and in gradient, using as an eluent, the mixtures detailed in each case, or by chromatotron (accelerated centrifugal radial chromatography) model 7924 with Merck silica gel plates 60 F254-366. For thin layer chromatography PL Merck F244 silica gel chromatofolios were used.
A solution of 1-methyl-2-{[methyl(prop-2-yn-1-yl)amino]methyl}-1H-indol-5-ol (8) (Cruces, M. A.; Elorriaga, C.; Fernández-Álvarez, E. Eur. J. Med. Chem. 1991, 26, 33-41) (0.215 g, 0.942 mmol), 1,2-dibromoethane (1.77 g, 9.42 mmol), and potassium carbonate (0.65 g, 4.71 mmol) in 2-butanone (8 mL) was heated at 85° C. for 6 h. The mixture was evaporated under vacuum and the residue was extracted with dichloromethane (10 mL) and water (10 mL). The organic phase was dried (Na2SO4) and evaporated. The residue was purified by column chromatography, eluting with a 4% methanol mixture in dichloromethane to give compound 9 (117.3 mg, 37%). Rf=0.76 (CH2Cl2/AcOEt, 10/1); pf 75-77° C.; RMN of 1H (300 MHz, CDCl3) δ 2.31 (t, J=2.4 Hz, 1H, ≡CH), 2.36 (s, 3H, N—CH3), 3.32 (d, J=2.4 Hz, 2H, N—CH2—C≡), 3.66 (t, J=6.4 Hz, 2H, —CH2—Br), 3.69 (s, 2H, N—CH2), 3.75 (s, 3H, N—CH3), 4.33 (t, J=6.4 Hz, 2H, —CH2—O—), 6.36 (s, 1H, CH3), 6.9 (dd, J=8.8, 2.5 Hz, 1H, CH6), 7.07 (d, J=2.4 Hz, 1H, CH4), 7.2 (d, J=8.8 Hz, 1H, CH7); RMN of 13C (75 MHz, CDCl3) δ 29.6 (CH2—Br), 29.9 (N—CH3), 41.5 (N—CH3), 44.7 (—CH2—C≡), 51.7 (CH2—N), 69.1 (CH2—O), 73.5 (≡CH), 78.3 (—C≡), 102.15 (CH3ind), 104.42 (CH4ind), 109.7 (CH7ind), 112.2 (CH6ind), 127.4 (C3aind), 133.8 (C7aind), 137.3 (C2ind), 152.2 (C5ind); EM (IE) m/z (%): 131 (48), 160 (66) [M-((Br(CH2)2)—NCH3CH2C≡CH)]+, 267 (100) [M-NCH3CH2C≡CH)]+, 334 (25)[M]+
Commercial 4-benzylpiperidine (36 μl, 0.2 mmol) was added to a suspension of 9 (34 mg, 0.1 mmol) and potassium carbonate (42 mg, 0.3 mmol) in DMF (1 mL). The mixture was heated at 80° C. overnight in an argon environment. The mixture was cooled, and it was poured over water (5 mL), and was extracted with dichloromethane (3×20 mL). The organic phase was dried (Na2SO4) and vacuum evaporated. The residue was purified by column chromatography, eluting with a 3.3% methanol mixture in dichloromethane to give compound 1 (33.5 mg, 77%). Rf=0.49 (CH2Cl2/MeOH, 10/1); RMN of 1H (400 MHz, CDCl3) δ 1.38 (qd, J=12.1 and 3.7 Hz, CH2), 1.56 (m, CH), 1.67 (d, J=12.8 Hz, CH2), 2.08 (td, J=11.7, 2.1 Hz, 1H, CH2), 2.31 (t, J=2.3 Hz, C≡CH), 2.35 (s, 3H, CH3), 2.56 (d, J=7.0 Hz, CH2), 2.83 (t, J=6.0 Hz, CH2), 3.034 (d, J=11.7 Hz, CH2), 3.32 (d, J=2.3 Hz, 2H, CH2), 3.68 (s, 2H, N—CH2), 3.74 (s, 3H, CH3), 4.16 (t, J=6.0 Hz, 2H, —CH2—O), 6.35 (s, 1H, CH), 6.88 (dd, J=8.8 and 2.4 Hz, 1H), 7.06 (d, J=2.3 Hz, 1H), 7.14-7.23 (m, 4H), 7.25-7.31 (m, 2H); RMN of 13C (100 MHz, CDCl3) δ 29.8 (CH3), 32.0 (2×CH2), 37.6 (CH), 41.5 (NCH3), 43.1 (CH2), 44.6 (CH2), 51.7 (CH2-indol), 54.2 (2×CH2), 57.6 (CH2), 66.6 (CH2—O), 73.4 (—C≡), 78.3 (≡CH), 102.0 (CH3ind), 103.4 (CH4ind), 109.5 (CH7ind), 111.0 (CH6ind), 125.7 (CHPh), 127.4 (C3aind), 128.0 (2×CHPh), 129.0 (2×CHPh), 133.3 (C7aind), 137.0 (C2ind), 140.60 (C1′Ph), 152.96 (C5ind); EM (IE) m/z (%): 188 (100), 202 (42), 429 (6)[M]+ (1.2×HCl): pf 218-220° C.; IR (KBr) ν 3421, 3189, 2929, 2498, 1619, 1486, 1208, 1163 cm−1. Anal. Calcd. for C28H37Cl2N3O+⅔H2O: C, 65.36; H, 7.51; N, 8.17.; Cl, 13.78. Found: C, 65.08; H, 7.74; N, 8.40.; Cl, 12.34.
Following the same procedure as for the synthesis of Compound 9,1-methyl-2-{[methyl(prop-2-yn-1-yl)amino]metal}-1H-indol-5-ol 8 (Cruces, M. A.; Elorriaga, C.; Fernández-Álvarez, E. Eur. J. Med. Chem. 1991, 26, 33-41) (21 mg, 0.092 mmol), was transformed into product 10 (25.4 mg, 80%). Rf=0.62 (CH2Cl2/AcOEt, 10/1); pf 71-72° C.; IR (KBr) ν 3275, 1488, 1468, 1206, 1026 cm−1; RMN of 1H (400 MHz, CDCl3) δ 2.30 (t, J=2.4 Hz, 1H, ≡CH), 2.33 [t, J=5.9 Hz, CH2—(CH2O)], 2.36 (s, 3H, N—CH3), 3.32 (d, J=2.4 Hz, 2H, CH2—C≡), 3.65 (t, J=6.5 Hz, 2H, —CH2—Br), 3.69 (s, 2H, ind-CH2—N), 3.75 (s, 3H, N—CH3), 4.14 (t, J=5.8 Hz, 2H, —CH2—OH), 6.35 (s, 1H, CH3), 6.87 (dd, J=8.8, 2.4 Hz, 1H, CH6), 7.07 (d, J=2.4 Hz, 1H, CH4), 7.2 (d, J=8.9 Hz, 1H, CH7); RMN of 13C (100 MHz, CDCl3) δ 29.8 (N—CH3), 30.3 (CH2—Br), 32.6 (CH2—(CH2O), 41.5 (N—CH3), 44.6 (CH2—C≡), 51.7 (CH2—N), 66.3 (CH2—O), 73.4 (≡CH), 78.3 (—C≡), 102.1 (CH3ind), 103.6 (CH4ind), 109.6 (CH7ind), 111.9 (CH6ind), 127.2 (C3aind), 133.5 (C7aind), 137.1 (C2ind), 152.8 (C5ind); EM (IE) m/z (%): 131 (60), 160 (100) [M-((Br(CH2)3)—CH3NCH2C≡CH)]+, 227 (7) [M-(Br(CH2)3)]+, 281 (96) [CH3NCH2C≡CH)]+, 348 (21)[M]+. Anal. Calcd. by (C17H21BrN2O) (348,0837): C, 58.46; H, 6.06; Br, 22.88; N, 8.02. Found: C, 58.49; H, 6.08; N, 22.11.; N, 8.23.
Following the same procedure as for the preparation of compound 2, starting from commercial 4-benzylpiperidine (0.11 mL, 0.63 mmol, 2 equiv) and compound 10 (111 mg, 0.31 mmol, 1 equiv), product 2 was obtained (89.2 mg, 64%): Rf=0.43 (CH2Cl2/MeOH, 10/1); pf 82-83° C.; IR (KBr) ν 3274, 2923, 1619, 1487, 1469, 1390, 1205, 1133, 1027 cm−1; RMN of 1H (400 MHz, CDCl3) δ 1.40 (qd, J=12.1, 3.2 Hz, CH2), 1.55 (m, CH), 1.66 (d, J=12.7 Hz, CH2), 1.92-2.08 (m, 4H, 2×CH2), 2.29 (t, J=2.3 Hz, C≡CH), 2.34 (s, 3H, CH3), 2.55 (d, J=6.7 Hz, CH2), 2.59 (t, J=7.3 Hz, CH2), 3.02 (d, J=11.4 Hz, CH2), 3.30 (d, J=2.3 Hz, 2H, CH2), 3.67 (s, 2H, CH2—N), 3.73 (s, 3H, CH3), 4.03 (t, J=6.2 Hz, 2H, —CH2—O), 6.32 (s, 1H, CH3ind), 6.83 (dd, J=8.8, 2.4 Hz, 1H, CH6ind), 7.02 (d, J=2.2 Hz, 1H, CH4ind), 7.12-7.21 (m, 4H), 7.25-7.31 (m, 2H); RMN of 13C (100 MHz, CDCl3) 26.7 (CH2), 29.8 (CH3), 31.7 (2×CH2), 37.7 (CH), 41.5 (N—CH3), 43.0 (CH2), 44.7 (CH2), 51.7 (CH2), 53.8 (2×CH2), 55.7 (CH2), 67.2 (CH2—O), 73.4 (—C≡), 78.3 (≡CH), 102.0 (CH3ind), 103.4 (CH4ind), 109.5 (CH7ind), 111.9 (CH6ind), 125.7 (CHPh), 127.4 (C3aind), 128.1 (2×CHPh), 129.0 (2×CHPh), 133.3 (C7aind), 137.0 (C2ind), 140.5 (C1′Ph), 153.1 (C5ind); EM (ES) m/z (%): 188 (99), 444 (100) [M+H]+, 445 (40) [M+2H]+, 466 (2)[M+Na]+. Anal. Calcd. for (C29H37N3O) (348,0837): C, 78.51; H, 8.41; N, 9.47.
Found: C, 78.63; H, 8.59; N, 9.44.
2. 2×HCl: pf 216-218° C.; IR (KBr) 3196, 2931, 2559, 2509, 1619, 1485, 1472, 1454, 1250, 1211, 1162 cm−1.
Following the same procedure, but starting from commercial 1-benzylpiperazine (0.148 g, 0.845 mmol) and 5-(3-bromopropoxy)-indole (10) (0.147 g, 0.422 mmol) the product 3 was obtained (0.16 g, 85%). Rf=0.43 (CH2Cl2/MeOH, 10/1); pf 103-4° C.; IR (KBr) ν 3138, 2958, 2943, 2806, 2762, 1621, 1492, 1480, 1207, 1159, 1003 cm−1; RMN of 1H (400 MHz, CDCl3) δ 2.01 [m, 2H, CH2(CH2O)], 2.32 (t, J=2.3 Hz, 1H, C≡CH), 2.36 (s, 3H, N—CH3), 2.53 (m, 8H, 4×CH2), 3.33 (d, J=2.3 Hz, 2H, CH2C), 3.54 (s, 2H, CH2—N), 3.69 (s, 2H, CH2Ph), 3.75 (s, 3H, N—CH3), 4.06 (t, J=6.4 Hz, 2H, —CH2O), 6.35 (s, 1H, CH3ind), 6.88 (dd, J=8.8, 2.4 Hz, 1H, CH6ind), 7.07 (d, J=2.4 Hz, 1H, CH4ind), 7.19 (d, J=8.8 Hz, 1H, CH7ind) 7.25-7.37 (m, 5H); RMN of 13C (100 MHz, CDCl3) 26.9 [CH2(CH2O)], 29.8 (N—CH3), 41.5 (N—CH3), 44.6 (CH2), 51.7 (CH2), 53.0 (2×CH2), 53.1 (CH2), 55.3, 63.0, 67.1 (CH2—O), 73.4 (—C≡), 78.3 (≡CH), 101.9 (CH3ind), 103.2 (CH4ind), 109.5 (CH7ind), 111.9 (CH6ind), 126.9 (CHPh), 127.4 (C3aind), 128.1 (2×CHPh), 129.1 (2×CHPh), 133.2 (C7aind), 136.9 (C2ind), 138.0 (C1′Ph), 153.1 (C5ind); EM (ES) m/z (%): 445 (100) [M+H]+, 467 (2) [M+Na]+. Anal. Calcd. for (C28H36N4O): C, 75.64; H, 8.16; N, 12.60.
Found: C, 75.39; H, 8.40; N, 12.52.
3. 3×HCl: pf 227-230° C.; IR (KBr) ν 3195, 2953, 2561, 2516, 2442, 1620, 1485, 1472, 1442, 1211, 1163 cm−1. Anal. Calcd. for (C28H39Cl3N4O+½(H2O)) (561.21): C, 59.73; H, 7.16; N, 9.95.; Cl, 18.89. Found: C, 59.59; H, 7.49; N, 10.20.; Cl, 18.53
A dissolution of 1-methyl-2-{[methyl(prop-2-yn-1-yl)amino]metal}-1H-indol-5-ol 8 (Cruces, M. A.; Elorriaga, C.; Fernández-Álvarez, E. Eur. J. Med. Chem. 1991, 26, 33-41) (0.21 g, 0.94 mmol) and 1-benzyl-4-(chloromethyl)piperidine 11 (Mohapatra, P. P.; Bhat, L. WO2008073452 (0.33 g, 1.51 mmol, 1.5 equiv) in dry acetonitrile (5 mL) NaH (60%) (120 mg, 3 equiv) (previously washed with dry hexane) was added in several portions. The mixture was heated at 50° C. for 10 h in an argon environment. The solvent was evaporated and the residue was diluted with dichloromethane. The mixture was washed with water and extracted with dichloromethane (3×20 mL). The organic phase was dried (Na2SO4) and vacuum evaporated. The residue was purified by column chromatography, eluting with a 1% methanol mixture in dichloromethane to give compound 4 (126.3 mg, 32%). Rf=0.24 (CH2Cl2/MeOH, 10/1); pf 123-5° C.; IR (KBr) ν 3252, 2938, 2913, 1620, 1489, 1466, 1195, 1163, 1029, 1008 cm−1; RMN DE 1H (400 MHz, CDCl3) δ 1.39-1.49 (m, 2H), 1.81-1.91 (m, 3H), 2.02 (t, J=16 Hz, 2H), 2.30 (t, J=2.2 Hz, C≡CH), 2.35 (s, 3H, N—CH3), 2.95 (d, J=11.4 Hz, 2H), 3.31 (d, 2H, J=2.2 Hz, CH2—C≡CH), 3.53 (s, 2H, CH2-Ph), 3.68 (s, 2H, ind-CH2—N), 3.73 (s, 3H, N—CH3), 3.85 (d, J=6.0 Hz, 2H, O—CH2—), 6.34 (s, 1H, CH-3), 6.86 (dd, J=8.8, 2.3 Hz, 1H, CH-6), 7.04 (d, J=2.3 Hz, 1H, CH-4), 7.18 (d, J=8.8 Hz, 1H, CH-7), 7.24-7.35 (m, 5H); RMN of 13C (100 MHz, CDCl3) 29.1 (2×CH2), 29.8 (ind-CH3), 35.9 (CH-piperidine), 41.5 (N—CH3), 44.6 (CH2—C≡), 51.7 (Ind-CH2—N), 53.4 (2×CH2), 63.4 (Ph-CH2), 54.0 (2×CH2), 63.4 (CH2-Ph), 73.4 (≡CH), 73.6 (CH2—O), 78.4 (—C≡), 102.0 (CH3ind), 103.3 (CH4ind), 109.5 (CH7ind), 111.9 (CH6ind), 126.8 (CH4′Ph), 127.5 (C3aind), 128.1 (2×CHPh), 129.1 (2×CHPh), 133.3 (C7aind), 137.8 (C2ind), 138.3 (C1′Ph), 153.3 (C5ind); EM (ES) m/z (%): 416 (100) [M+H]+, 438 (2) [M+Na]+
4.2×HCl: pf 230-3° C.; IR (KBr) ν 3423, 3200, 2933, 2511, 1620, 1486, 1466, 1208, cm−1. Anal. Calcd. for C27H35Cl2N3O: C, 66.39; H, 7.22; N, 8.60.; Cl, 14.52. Found: C, 66.21; H, 7.43; N, 8.63.; Cl, 14.42.
Following the same procedure, but starting from 1-benzyl-4-(2-chloroethyl)piperidine 12 (Contreras, J.-M.; Parrot, I.; Sippl, W.; Rival, Yveline M.; Wermuth, C. G. J. Med. Chem. 2001, 44, 2707-2718) (0.25 g, 1.05 mmol, 1.5 equiv) and 1-methyl-2-{[methyl(prop-2-yn-1-yl)amino]metal}-1H-indol-5-ol 8 (Cruces, M. A.; Elorriaga, C.; Fernández-Álvarez, E. Eur. J. Med. Chem. 1991, 26, 33-41) (160 mg, 0.7 mmol) in dry DMF (5 mL), product 5 was obtained (0.216 g, 72%): Rf=0.27 (CH2Cl2/MeOH, 10/1); pf 86-7° C.; RMN of 1H (400 MHz, CDCl3) δ 1.31-1.41 (m, 2H), 1.52-162 (m, CH), 1.72-1.77 (m, 4H), 2.0 (t, J=10.8, 2H), 2.29 (t, J=2.3 Hz, C≡CH), 2.34 (s, 3H, N—CH3), 2.91 (d, J=11.6 Hz, 2H), 3.31 (d, 2H, J=2.3 Hz, CH2—C≡CH), 3.52 (s, 2H, CH2-Ph), 3.67 (s, 2H, N—CH2), 3.74 (s, 3H, N—CH3), 4.03 (t, J=6.5 Hz, 2H, O—CH2—), 6.33 (s, 1H, CH-3), 6.85 (dd, J=8.8, 2.4 Hz, 1H, CH-6), 7.03 (d, J=2.4 Hz, 1H, CH-4), 7.18 (d, J=8.8 Hz, 1H, CH-7), 7.23-7.34 (m, 5H); RMN of 13C (100 MHz, CDCl3) δ0.1 (N—CH3), 32.4 (CH2), 32.8 (CH2), 36.2 (CH2), 41.8 (N—CH3), 44.9 (CH2—C CH), 52.0 (CH2-ind), 53.9 (2×CH2), 63.6 (CH2-Ph), 66.7 (CH2—O), 73.68 (═CH), 78.6 (—C≡), 102.0 (CH3ind), 103.5 (CH4ind), 109.5 (CH7ind), 112.2 (CH6ind), 127.2 (CHPh), 127.7 (C3aind), 128.3 (2×CHPh), 129.5 (2×CHPh), 133.6 (C7aind), 137.2 (C2ind), 138.4 (C1′Ph), 153.5 (C5ind); EM (IE) m/z (%): 91 (48) [PhCH2]+, 202 (100), 361 (3) [M-NCH3CH2C≡CH)]+, 429 (4) [M]+. Anal. Calcd. for (C28H35N3O) (429, 2780): C, 78.28; H, 8.21; N, 9.78.
Found: C, 77.99; H, 8.45; N, 9.79.
5.2×HCl: pf 221-3° C.; IR (KBr) ν 3424, 3195, 2928, 2561, 2506, 1619, 1486, 1471, 1210, cm−1. Anal. Calcd. for C28H37Cl2N3O+⅓H2O: C, 66.13; H, 7.47; N, 8.26.; Cl, 13.94. Found: C, 66.04; H, 7.89; N, 8.59.; Cl, 13.84.
Following the same procedure, but starting from 1-benzyl-4-(3-chloropropyl)piperidine 13 (0.36 g, 1.44 mmol, 1.5 equiv) and 1-methyl-2-{[methyl(prop-2-yn-1-yl)amino]metal}-1H-indol-5-ol 8 (Cruces, M. A.; Elorriaga, C.; Fernández-Álvarez, E. Eur. J. Med. Chem. 1991, 26, 33-41) (0.22 g, 0.96 mmol) in dry DMF (5 mL), product 6 was obtained (0.268 g, 63%): RF 0.28 (CH2Cl2/MeOH, 20/1); pf 90-1° C.; IR (KBr) ν 3265, 2935, 2908, 2799, 2760, 1619, 1489, 1471, 1395, 1269, 1204, 1190, 1160, 1029 cm−1; RMN of 1H (400 MHz, CDCl3) δ 1.29-1.31 (m, 3H, CH+CH2), 1.41-1.46 (m, 2H, CH2—(CH2)2O), 1.72 (d, J=9.1 Hz, 2H, CH2), 1.83 (m, 2H, CH2—CH2O), 1.97 (t, J=12 Hz, 2H, CH2), 2.31 (t, J=2.0 Hz, C≡CH), 2.36 (s, 3H, N—CH3), 2.91 (d, J=10.8 Hz, CH2), 2.33 (d, J=2.2 Hz, 2H, CH2—C≡CH), 3.52 (s, 2H, CH2-Ph), 3.69 (s, 2H, ind-CH2), 3.75 (s, 3H, ind-CH3), 3.98 (t, J=6.6 Hz, 2H, O—CH2—), 6.35 (s, 1H, CH-3), 6.85 (dd, J=8.8 and 2.3 Hz, 1H, CH-6), 7.05 (d, J=2.14 Hz, 1H, CH-4), 7.19 (d, J=8.8 Hz, 1H, CH-7), 7.25-7.35 (m, 5H, Ph); RMN of 13C (100 MHz, CDCl3) δ 26.7 (CH2—CH2O), 29.8 (ind-N—CH3), 32.2 (2CH2), 32.8 [CH2—(CH2)2O], 35.5 (CH-piperidine), 41.5 (N—CH3), 44.6 (CH2—C), 51.7 (ind-CH2), 53.8 (2×CH2), 63.4 (CH2-Ph), 69.0 (CH2—O), 73.4 (≡CH), 78.3 (—C≡), 102.0 (CH3ind), 103.3 (CH4ind), 109.5 (CH7ind), 112.0 (CH6ind), 126.8 (CHPh), 127.4 (C3aind), 128.0 (2×CHPh), 129.2 (2×CHPh), 133.32 (C7aind), 136.9 (C2ind), 138.3 (C1′Ph), 153.26 (C5ind); EM (IE) m/z (%): 91 (77) [PhCH2]+, 352 (22) [M-CH2Ph]+, 374 (100) [M-NCH3CH2C≡CH)]+, 404 (7) [M-CH2C≡CH)]+, 428 (5) [M-CH3]+, 443 (40)[M]+. Anal. Calcd. for C29H37N3O): C, 78.51; H, 8.41; N, 9.47. Found: C, 78.36; H, 8.31; N, 9.23.
6.2×HCl: pf 203-5° C.; IR (KBr) 3193, 2937, 2512, 1619, 1486, 1469, 1209 cm−1. Anal. Calcd. for C29H39Cl2N3O: (516.55): C, 67.43; H, 7.61; N, 8.13.; Cl, 13.73.
Found: C, 67.38; H, 7.81; N, 8.02.; Cl, 13.13.
Following the same procedure, but starting from 1-benzyl-4-(4-chloropropyl)piperidine 14 (0.5 g, 1.88 mmol, 1.2 equiv) and 1-methyl-2-{[methyl(prop-2-yn-1-yl)amino]metal}-1H-indol-5-ol 8 (Cruces, M. A.; Elorriaga, C.; Fernández-Álvarez, E. Eur. J. Med. Chem. 1991, 26, 33-41) (0.358 g, 1.56 mmol) in dry DMF (8 mL), product 7 was obtained (0.547 g, 76%): Rf=0.28 (CH2Cl2/MeOH, 20/1); pf 93-4° C.; IR (KBr) ν 3260, 2937, 2918, 1619, 1489, 1472, 1203, 1193, 1160, 1008 cm−1; RMN of 1H— (500 MHz, CDCl3) δ 1.22-134 [m, 4H, CH2pip+CH2—(CH2)3], 1.45-1.51 (m, 2H, CH2—(CH2)2O), 1.66 (br d, J=9.4 Hz, CH2pip), 1.73-183 (m, 2H, CH2—CH2O) 1.85-2.00 (m, CH2pip), 2.28 (t, J=2.4 Hz, C≡CH), 2.34 (s, 3H, N—CH3), 2.88 (d, J=10.5 Hz, CH2pip), 3.31 (d, J=2.4 Hz, 2H, CH2—C≡CH), 3.49 (s, 2H, CH2-Ph), 3.67 (s, 2H, CH2—N), 3.73 (s, 3H, N—CH3), 3.98 (t, J=6.6 Hz, 2H, —CH2—O—), 6.32 (s, 1H, CH-3), 6.85 (dd, J=8.8 and 2.4 Hz, 1H, CH6ind), 7.03 (d, J=2.3 Hz, 1H, CH4ind), 7.17 (d, J=8.8 Hz, 1H, CH7ind), 7.23-7.32 (m, 5H); RMN of 13C (125 MHz, CDCl3) δ 23.3 [CH2—(CH2)2O], 29.7 (CH2—CH2O), 29.8 (Nind-CH3), 32.3 (2×CH2pip), 35.69 (CH), 36.3 CH2—(CH2)3O], 41.7 (N—CH3), 44.7 (CH2—C CH), 51.8 (N—CH2-ind), 53.9 (2×CH2pip), 63.5 (CH2-Ph), 68.8 (CH2—O), 73.4 (≡CH), 78.4 (—C≡), 102.0 (CH3ind), 103.4 (CH4ind), 109.5 (CH7ind), 112.0 (CH6ind), 126.8 (CHPh), 127.5 (C3aind), 128.1 (2×CHPh), 129.2 (2×CH2Ph), 133.3 (C7aind), 137.0 (C2ind), 138.5 (C1′Ph), 153.52 (C5ind); EM (IE) m/z (%): 91 (55) [PhCH2]+, 172 (71), 228 (45), 366 (41) [MBz]+, 388 [M-NCH3CH2C≡CH)]+, 418 (8) [M-CH2C≡CH)]+, 457 (26) [M]+. Anal. Calcd. for C30H39N3O: C, 78.73; H, 8.59; N, 9.18. Found: C 78.65; H, 8.71; N, 9.07.
7.2×HCl: pf 197-9° C.; IR (KBr) ν 3421, 3195, 2928, 2851, 2561, 2509, 1619, 1485, 1472, 1458, 1408, 1209, 1160 cm−1. Anal. Calcd. for (C30H39N3O.2HCl) (529, 26): C, 67.91; H, 7.79; Cl, 13.36; N, 7.92. Found: C, 67.54; H, 7.45; Cl, 13.25; N, 8.10;
The inhibitory activity of the enzyme acetylcholinesterase (AChE) was evaluated by the Ellman method (Biochem. Pharmacol. 1961, 7, 88) using an electric eel as an AChE neuronal model (Electrophorus electricus) and acetylthiocholine iodide (0.35 mM) as substrate. The reaction took place in a final volume of 3 mL of a 0.1 M phosphate buffer solution, pH 8.0, containing 0.035 units of AChE and used a 0.35 mM solution of 5,5′-dithio-bis(2-nitrobenzoic acid) (DTNB) to produce the 5-thio-2-nitrobenzoic acid anion. Inhibition curves were performed in triplicate by incubating at least nine inhibitor concentrations for 10 min. A triplicate sample without inhibitor was always present so as to be aware of 100% of the AChE activity. After this time, the substrate was added to 0.35 mM acetylthiocholine iodide, from a 10 mM stock solution. Loss of color was observed at 412 nm in a spectrophotometric reader having 96 well plates. Determinations of BuChE inhibitory activity, extracted from horse serum, were performed similarly, using 0.05 units/ml BuChE, 0.35 mM 5,5′-dithio-bis-2-nitrobenzoic acid (DTNB) and 0.5 mM butyrylthiocholine iodide from a 10 mM stock solution in a final volume of 3 mL. A triplicate sample without inhibitor was always present so as to be aware of 100% of the BuChE activity. Data from concentration-inhibition experiments of the inhibitors was calculated by non-linear regression analysis using the Origin package which gives estimates of the IC50 (drug concentration producing 50% inhibition of enzyme activity). The results are expressed as Mean±S.E.M. of at least four experiments performed in triplicate. DTNB, acetylthiocholine iodide, butyrylthiocholine iodide.
The inhibitory activity of monoamine oxidases A and B was assessed by the Fowler and Tipton radiometric method (Biochem Pharmacol 1981, 30, 3329) using a purification of rat liver mitochondria as the source of enzymes. The inhibitory activity of MAO-B was compared to 25 μl of [14C]-phenylethylamine (PEA), 20 μM of activity, 2.5 mCi/mmol. The inhibitory activity of MAO-A was compared to 25 μl of [14C]-(5-hydroxytriptamine) (5-HT), 100 μM of activity, 0.5 mCi/mmol. Inhibition curves were performed in triplicate by incubating at least nine inhibitor concentrations for 30 min. A triplicate sample without inhibitor was always present so as to be aware of 100% of the MAO activity. The reaction took place with the addition of the substrate in a final volume of 225 μl of 50 mM phosphate buffer, pH 7.4, containing 20 μl of rat liver mitochondria at a concentration of 5 mg/ml. The reaction was carried out under continuous stirring at 37° C. for 4 minutes in the case of MAO-B and 20 minutes in the case of MAO-A. The test ended with the addition of 100 μl of 2M citric acid. The aldehydes produced were obtained after adding 4 ml of a solution of toluene:ethyl acetate (1:1, v/v) containing 0.6% (w/v) 2-5-diphenyloxazole (PPO) and the vials were stirred for 1 minute leaving them at −80° C. for 20 min. Thus, freezing was produced in the aqueous phase, where the substrate is not metabolized, and the organic phase was decanted where the aldehyde produced. The radioactivity of the organic phase was read on a Tri-Garb 2810TR scintillation counter, with a counting time of 1 minute per vial. From the disintegration per minute (dpm) data obtained, the specific enzyme activity was calculated (pmol/min·mg protein) with the following equation:
dpm·(100/X)·Y·(1/t min reaction)·(1/μl prot)·(1000/P)=pmol/min·mg prot
X is the extraction ratio of the aldehyde in the organic phase {Fowler, 1980 57/id}, and it is 74.4% for the serotonin aldehyde and 92.5% for the phenylethylamine aldehyde. Y is the dpm to pmol conversion factor, which depends on the activity of the substrate and is 0.9 for serotonin and 0.18 for phenylethylamine. Lastly, P is the concentration of protein used expressed in mg/ml.
The analysis data were calculated by nonlinear regression, sigmoidal dose-response, using GraphPad Prism 3.0 program from which the IC50 estimates were obtained for each of the inhibitors. The results were expressed as Mean±SEM of at least three experiments performed in triplicate.
| Number | Date | Country | Kind |
|---|---|---|---|
| P201030404 | Mar 2010 | ES | national |
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/ES11/70186 | 3/18/2011 | WO | 00 | 9/18/2012 |
