WO2010015324A1 - Quinuclidine carbonate derivatives and medicinal composition thereof - Google Patents
Quinuclidine carbonate derivatives and medicinal composition thereof Download PDFInfo
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- WO2010015324A1 WO2010015324A1 PCT/EP2009/005272 EP2009005272W WO2010015324A1 WO 2010015324 A1 WO2010015324 A1 WO 2010015324A1 EP 2009005272 W EP2009005272 W EP 2009005272W WO 2010015324 A1 WO2010015324 A1 WO 2010015324A1
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- 0 *[N+]1(CCC2CC1)CC2OC(O*)=O Chemical compound *[N+]1(CCC2CC1)CC2OC(O*)=O 0.000 description 2
- KWJWMWZXULCUAC-UHFFFAOYSA-O COc1cc(C(c2cccc(F)c2)OC([OH+]C2C(CC3)CCN3C2)=O)ccc1 Chemical compound COc1cc(C(c2cccc(F)c2)OC([OH+]C2C(CC3)CCN3C2)=O)ccc1 KWJWMWZXULCUAC-UHFFFAOYSA-O 0.000 description 1
- XJOJRYKMTYPSCO-BOBCHSRXSA-N C[N+]1(CCC2CC1)C[C@@H]2OC(OC1c2ccccc2-c2ccccc12)=O Chemical compound C[N+]1(CCC2CC1)C[C@@H]2OC(OC1c2ccccc2-c2ccccc12)=O XJOJRYKMTYPSCO-BOBCHSRXSA-N 0.000 description 1
- HVSCFCGEVKEGME-DHHCDUQHSA-N C[N+]1(CCC2CC1)C[C@@H]2OC(Oc1ccccc1-c1ccccc1)=O Chemical compound C[N+]1(CCC2CC1)C[C@@H]2OC(Oc1ccccc1-c1ccccc1)=O HVSCFCGEVKEGME-DHHCDUQHSA-N 0.000 description 1
- CQZLRWOSWDGGGK-BSDXKTKUSA-O NC(C[N+]1(CCC2CC1)C[C@@H]2OC(OC(c1cc(F)ccc1)c1cc(F)ccc1)=O)=O Chemical compound NC(C[N+]1(CCC2CC1)C[C@@H]2OC(OC(c1cc(F)ccc1)c1cc(F)ccc1)=O)=O CQZLRWOSWDGGGK-BSDXKTKUSA-O 0.000 description 1
- QNIJGMHROIATIS-LNJRRRJYSA-N O=C(C[N+]1(CCC2CC1)C[C@@H]2OC(OC(C1CCCCC1)c1cc(F)ccc1)=O)c1ccc[s]1 Chemical compound O=C(C[N+]1(CCC2CC1)C[C@@H]2OC(OC(C1CCCCC1)c1cc(F)ccc1)=O)c1ccc[s]1 QNIJGMHROIATIS-LNJRRRJYSA-N 0.000 description 1
- WXYFAXVCOBKXFQ-HIVDTEPYSA-N O=C(C[N+]1(CCC2CC1)C[C@@H]2OC(OC(c1cccc(F)c1)c1cc(F)ccc1)=O)c1ccncc1 Chemical compound O=C(C[N+]1(CCC2CC1)C[C@@H]2OC(OC(c1cccc(F)c1)c1cc(F)ccc1)=O)c1ccncc1 WXYFAXVCOBKXFQ-HIVDTEPYSA-N 0.000 description 1
- UBQHLTBTGOPPDS-DPXQPOCBSA-N O=C(C[N+]1(CCC2CC1)C[C@@H]2OC(OC(c1ccccc1Cl)c(cccc1)c1Cl)=O)c1ccc[s]1 Chemical compound O=C(C[N+]1(CCC2CC1)C[C@@H]2OC(OC(c1ccccc1Cl)c(cccc1)c1Cl)=O)c1ccc[s]1 UBQHLTBTGOPPDS-DPXQPOCBSA-N 0.000 description 1
- ZMPGNXHUYROCKW-DWVUQKNYSA-N O=C(C[N+]1(CCC2CC1)C[C@@H]2OC(OCc(cc1)ccc1F)=O)c1ccc[s]1 Chemical compound O=C(C[N+]1(CCC2CC1)C[C@@H]2OC(OCc(cc1)ccc1F)=O)c1ccc[s]1 ZMPGNXHUYROCKW-DWVUQKNYSA-N 0.000 description 1
- PCBRVNGHCJLVEM-OTBAGVBSSA-N O=C(C[N+]1(CCC2CC1)C[C@@H]2OC(Oc1ccccc1-c1ccccc1)=O)c1ccc[s]1 Chemical compound O=C(C[N+]1(CCC2CC1)C[C@@H]2OC(Oc1ccccc1-c1ccccc1)=O)c1ccc[s]1 PCBRVNGHCJLVEM-OTBAGVBSSA-N 0.000 description 1
- NARHBLOHLSVCMM-IBGZPJMESA-N O=C(OC(c(cc1)ccc1Cl)c(cc1)ccc1Cl)O[C@@H]1C(CC2)CCN2C1 Chemical compound O=C(OC(c(cc1)ccc1Cl)c(cc1)ccc1Cl)O[C@@H]1C(CC2)CCN2C1 NARHBLOHLSVCMM-IBGZPJMESA-N 0.000 description 1
- DLAJBUFIBNHWSA-OQNFHVEWSA-N O=C(OC1c2ccccc2-c2c1cccc2)O[C@@H]1C(CC2)CC[N+]2(CC2=CC=CCC2)C1 Chemical compound O=C(OC1c2ccccc2-c2c1cccc2)O[C@@H]1C(CC2)CC[N+]2(CC2=CC=CCC2)C1 DLAJBUFIBNHWSA-OQNFHVEWSA-N 0.000 description 1
- SSDFKFNINOCBQC-AWEZNQCLSA-N O=C(OCc1cccc(Br)c1)O[C@@H]1C(CC2)CCN2C1 Chemical compound O=C(OCc1cccc(Br)c1)O[C@@H]1C(CC2)CCN2C1 SSDFKFNINOCBQC-AWEZNQCLSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D453/00—Heterocyclic compounds containing quinuclidine or iso-quinuclidine ring systems, e.g. quinine alkaloids
- C07D453/02—Heterocyclic compounds containing quinuclidine or iso-quinuclidine ring systems, e.g. quinine alkaloids containing not further condensed quinuclidine ring systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/04—Drugs for disorders of the respiratory system for throat disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/06—Antiasthmatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/08—Bronchodilators
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
Definitions
- the present invention relates to quinuclidine carbonate derivatives acting as muscarinic receptor antagonists, processes for the preparation of such derivatives, compositions comprising them and the therapeutic use thereof.
- Quaternary ammonium salts acting as muscarinic (M) receptors antagonists drugs are currently used in therapy to induce bronchodilation for the treatment of respiratory diseases.
- M receptor antagonists drugs are represented by ipratropium bromide and tiotropium bromide.
- Said M and M3 receptors antagonists drugs are currently administered through inhalation in order to deliver the drug directly at the site of action and hence limiting the systemic exposure.
- the known compounds may still exhibit undesired side effects due to systemic absorption.
- M3 receptor antagonists drugs able to act locally, while having high potency and long duration of action. Said drugs, once adsorbed, are degraded to inactive compounds which are deprived of any systemic side effects typical of muscarinic antagonists.
- the present invention provides quinuclidine carbonate derivatives with these therapeutically desirable characteristics.
- the compounds of general formula (I) behave as soft-drugs, since they are able to produce a persistent bronchodilating effect in the lung but are consistently and rapidly transformed into inactive metabolites after passing into human plasma. This behaviour gives great advantages in terms of safety.
- the invention is directed to quinuclidine carbonate derivatives of general formula (I)
- A may be optionally substituted aryl or heteroaryl or arylalkyl or heteroarylalkyl or a group of formula (a)
- Z is selected from CO, O, COO, OCO, SO 2 , S, SO, COS and SCO or it is a bond and
- Ri is a residue selected from:
- - aryl optionally substituted with NR 2 CO-(Ci-Cio)-alkyl, (Ci-Cio)-alkyl, O-(Ci-Cio)-alkyl or halogen and - heteroaryl optionally substituted with NR 2 CO-(Ci-Cio)-alkyl or halogen.
- R 2 is a group selected from H, phenoxycarbonyl, benzyloxycarbonyl, (Ci-Cio)-alkoxycarbonyl, (d-Cio)-alkylcarbonyl, (Ci-Cio)-alkylsulfonyl and (Ci-Cio)-alkyl.
- X- is a physiologically acceptable anion.
- the present invention also provides pharmaceutical compositions of compounds of formula (I) alone or in combination with or in mixture with one or more pharmaceutically acceptable carriers and/or excipients.
- the present invention also provides the use of compounds of formula (I) for preparing a medicament.
- the invention provides the use of compounds of formula (I) for the prevention and/or treatment of any broncho-obstructive or inflammatory disease, preferably asthma or chronic bronchitis or chronic obstructive pulmonary disease (COPD).
- any broncho-obstructive or inflammatory disease preferably asthma or chronic bronchitis or chronic obstructive pulmonary disease (COPD).
- COPD chronic obstructive pulmonary disease
- the invention provides the use of compounds of formula (I) for the manufacture of a medicament for the prevention and/or treatment of any broncho-obstructive or inflammatory disease, preferably asthma or chronic bronchitis or chronic obstructive pulmonary disease (COPD).
- any broncho-obstructive or inflammatory disease preferably asthma or chronic bronchitis or chronic obstructive pulmonary disease (COPD).
- COPD chronic obstructive pulmonary disease
- the present invention further provides a method for prevention and/or treatment of any broncho-obstructive or inflammatory disease, preferably asthma or chronic bronchitis or chronic obstructive pulmonary disease (COPD), which comprises administering to a subject in need thereof a therapeutically effective amount of a compound of general formula (I).
- the present invention also provides pharmaceutical compositions suitable for administration by inhalation.
- lnhalable preparations include inhalable powders, propellant-containing metering aerosols or propellant-free inhalable formulations.
- the invention is also directed to a device which may be a single- or multi-dose dry powder inhaler, a metered dose inhaler and a soft mist nebulizer comprising the compounds of formula (I).
- the invention is also directed to a kit comprising the pharmaceutical compositions of compounds of formula (I) alone or in combination with or in admixture with one or more pharmaceutically acceptable carriers and/or excipients and a device which may be a single- or multi-dose dry powder inhaler, a metered dose inhaler and a soft mist nebulizer comprising the compounds of general formula (I).
- a kit comprising the pharmaceutical compositions of compounds of formula (I) alone or in combination with or in admixture with one or more pharmaceutically acceptable carriers and/or excipients and a device which may be a single- or multi-dose dry powder inhaler, a metered dose inhaler and a soft mist nebulizer comprising the compounds of general formula (I).
- halogen atoms as used herein includes fluorine, chlorine, bromine, and iodine.
- (C1-C10) alkyl refers to straight-chained and branched alkyl groups wherein the number of carbon atoms is from 1 to 10. Examples of groups are methyl, ethyl, n-propyl, isopropyl, t-butyl, pentyl, hexyl, heptyl, octanyl, nonenyl and decenyl.
- one or more hydrogen atoms in said groups can be replaced by halogen atoms.
- the derived expressions "(Ci-Cio)-alkoxycarbonyl", "(Ci- Cio)-alkylsulfanyl”, “(Ci-Cio)-alkylsulfinyl”, “(Ci-Cio)-alkylsulfonyl” and "(Ci- Cio)-alkoxyl" are to be construed in an analogous manner.
- alicyclic compounds includes: - "(C3-C8)-cycloalkyl", which refers to cyclic non-aromatic isolated hydrocarbon saturated groups. Examples include cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl and cyclooctenyl;
- Bicycloalkyl and tricycloalkyl which are non-aromatic saturated cyclic alkyl moieties consisting of two or three rings, respectively, wherein said rings share at least one carbon atom.
- bicycloalkyl groups include spiro rings and fused rings.
- bicycloalkyl groups include, but are not limited to, bicyclo- [3. 1. 0]-hexyl, bicyclo- [2.2. 1]-hept-1-yl, norbornyl, spiro [4. 5] decyl, spiro [4.4] nonyl, spiro [4. 3] octyl, and spiro [4. 2] heptyl.
- An example of a tricycloalkyl group is adamantanyl; and - cyclic non-aromatic hydrocarbon unsaturated groups. Examples include cyclohexenyl, norbornenyl, bicyclo [2.2.1.]heptanyl.
- one or more hydrogen atoms in said groups can be replaced by one or more halogen atoms.
- aryl refers to mono, bi- or tricyclic ring systems having 5 to 20, preferably from 5 to 15, ring atoms, and wherein at least one ring is aromatic.
- one or more hydrogen atoms in said rings can be replaced by one or more halogen atoms or phenyl.
- heteroaryl refers to mono, bi- or tricyclic ring systems having 5 to 20, preferably from 5 to 15, ring atoms, in which at least one ring is aromatic and in which at least one ring atom is a heteroatom (e.g. N, S or O).
- ring atoms e.g. N, S or O
- one or more hydrogen atoms in said rings can be replaced by one or more halogen atoms.
- arylalkyl refers to a "(C1-C4) alkyl” optionally substituted by a mono, bi- or tricyclic ring systems which have 5 to 20, preferably from 5 to 15, ring atoms.
- one or more hydrogen atoms in said rings can be replaced by one or more halogen atoms.
- Suitable arylalkyl groups include benzyl, biphenylmethyl and thiophenylmethyl.
- heteroarylalkyl refers to a "(C1-C4) alkyl” optionally substituted by a mono, bi- or tricyclic ring systems which have 5 to 20 ring atoms, preferably from 5 to 15, in which at least one ring is aromatic and in which at least one ring atom is a heteroatom (e.g. N, S or O).
- a heteroatom e.g. N, S or O.
- one or more hydrogen atoms in said rings can be replaced by one or more halogen atoms.
- Suitable monocyclic systems include thiophene, cyclopentadiene, benzene, pyrrole, pyrazole, imidazole, isoxazole, oxazole, isothiazole, thiazole, pyridine, imidazolidine, piperidine and furan radicals.
- bicyclic systems examples include naphthalene, biphenyl, purine, pteridine, benzotriazole, quinoline, isoquinoline, indole, isoindole and benzothiophene radicals.
- Suitable tricyclic systems include fluorene radicals. DETAILED DESCRIPTION OF THE INVENTION
- the invention is directed to quinuclidine carbonate derivatives acting as muscarinic receptors antagonists, and to salts thereof, said derivatives preferably acting on the M3 receptors.
- physiologically acceptable anions X include those selected from the group consisting of chloride, bromide, iodide, sulfate, phosphate, methanesulfonate, nitrate, maleate, acetate, citrate, fumarate, tartrate, oxalate, succinate, benzoate, and p-toluenesulfonate, preferably chloride, bromide and iodide, more preferably chloride and bromide.
- a preferred group of compounds of formula (I) is that wherein R is (Ci-C6)-alkyl substituted by -Z-Ri, wherein Z and Ri are as described above.
- Another preferred group of compounds of formula (I) is that wherein R is (Ci-C6)-alkyl substituted by -Z-Ri, wherein Z is O, CO or a bond and Ri is aryl or heteroaryl as described above, preferably substituted with one or more halogen atoms.
- a more preferred group of compounds of formula (I) is that wherein R is CH2, Z is CO and Ri is thienyl, according to formula (II):
- a first group of compounds of formula (II) is represented by the compounds wherein A is optionally substituted aryl or heteroaryl or arylalkyl or heteroarylalkyl or a group of formula (a)
- R3 and R 4 are both independently aryl or heteroaryl, preferably substituted with one or more halogen atoms.
- a second group of compounds of formula (II) is represented by the compounds wherein A is a group of formula (a), wherein R3 and R 4 are both phenyl, preferably substituted with one or more halogen atoms.
- a fourth group of compounds of formula (II) is represented by the compounds wherein A is a 9H-fluoren-9-yl, preferably substituted with one or more halogen atoms.
- a fifth group of compounds of formula (II) is represented by the compounds wherein A is an arylalkyl, preferably a phenyl-(Ci-C4)-alkyl, more preferably substituted with one or more halogen atoms and even more preferably A is a benzyl, optionally substituted with one or more halogen atoms.
- a sixth group of compounds of formula (II) is represented by the compounds wherein A is a biphenylmethyl, preferably substituted with one or more halogen atoms.
- a seventh group of compounds of formula (II) is represented by the compounds wherein A is a thiophenylmethyl, preferably substituted with one or more halogen atoms.
- R is a propyl substituted by -Z-Ri group wherein Z is O and Ri is phenyl, according to formula (III):
- a first group of compounds of formula (III) is represented by the compounds wherein A is optionally substituted aryl or heteroaryl or arylalkyl or heteroarylalkyl or a group of formula (a)
- R3 and R 4 are both independently aryl or heteroaryl, preferably substituted with one or more halogen atoms.
- a second group of compounds of formula (III) is represented by the compounds wherein A is a group of formula (a), wherein R3 and R 4 are both phenyl, preferably substituted with one or more halogen atoms.
- a fourth group of compounds of formula (III) is represented by the compounds wherein A is a 9H-fluoren-9-yl, preferably substituted with one or more halogen atoms.
- a fifth group of compounds of formula (III) is represented by the compounds wherein A is arylalkyl, preferably a phenyl-(Ci-C 4 )-alkyl, more preferably substituted with one or more halogen atoms and even more preferably A is a benzyl, optionally substituted with one or more halogen atoms.
- a sixth group of compounds of formula (III) is represented by the compounds wherein A is a biphenylmethyl, preferably substituted with one or more halogen atoms.
- a seventh group of compounds of formula (III) is represented by the compounds wherein A is a thiophenylmethyl, preferably substituted with one or more halogen atoms.
- R is a methyl substituted by -Z-Ri group wherein Z is CO and Ri is phenyl, according to formula (IV):
- the active compound (I) shows at least one chiral center, which is represented by the quinuclidine carbon atom bearing the carbonate group.
- the active compound (I) is in the form of the substantially pure (R)-enantiomer, wherein the enantiomeric purity is higher than 85%, more preferably than 90%, more preferably than 95% and even more preferably than 99%.
- the present invention provides the compounds reported below:
- the compounds of formula (I) may be prepared according to known methods. Some of the processes which can be used are described below and reported in Scheme.
- the compounds of general formula (I) may be prepared according to a general process which includes the following steps:
- 1 st step - An amino-alcohol of formula (2) is reacted with 1,1'-carbonyldiimidazole (1) in an aprotic solvent.
- the reaction is carried out in a solvent selected from CH3CN, CH2CI2, CHCb, tetrahydrofuran (THF) and dioxane at a temperature ranging from 0 0 C to the boiling point of the solvent.
- Water is added and the imidazole derivative (3) is extracted with a solvent.
- solvents which can be suitably used are ethyl acetate, diethyl ether, methylene chloride;
- the solvent is evaporated to dryness and the residue is reacted with an alcohol of formula (4) in an aprotic solvent.
- the solvent is selected from THF, dimethylformamide (DMF), dimethylacetal (DMA).
- the alcohol is activated with a base advantageously selected from NaH, BuLi (butyl lithium), lithium diisopropylamide (LDA), to give a compound of formula (5).
- Compounds of formula (5) may be alkylated at the nitrogen atom of the tertiary amine by means of an alkylating agent RX wherein R is as previously defined and X is, according to known conditions, chlorine, bromine, or iodine, giving a quaternary ammonium salt of formula (I).
- RX alkylating agent
- X is, according to known conditions, chlorine, bromine, or iodine, giving a quaternary ammonium salt of formula (I).
- the invention also provides pharmaceutical compositions of compounds of formula (I) in admixture with one or more pharmaceutically acceptable carriers, for example those described in Remington's Pharmaceutical Sciences Handbook, XVII Ed., Mack Pub., N.Y., U.S.A.
- Administration of the compounds of the present invention may be accomplished according to patient needs, for example, orally, nasally, parenterally (subcutaneously, intravenously, intramuscularly, intrasternally and by infusion), by inhalation, rectally, vaginally, topically, locally, transdermal ⁇ , and by ocular administration.
- solid oral dosage forms can be used for administering compounds of the invention including such solid forms as tablets, gelcaps, capsules, caplets, granules, lozenges and bulk powders.
- the compounds of the present invention can be administered alone or combined with various pharmaceutically acceptable carriers, diluents (such as sucrose, mannitol, lactose, starches) and known excipients, including suspending agents, solubilizers, buffering agents, binders, disintegrants, preservatives, colorants, flavorants, lubricants and the like.
- Time release capsules, tablets and gels are also advantageous in administering the compounds of the present invention.
- liquid oral dosage forms can also be used for administering compounds of the invention, including aqueous and non-aqueous solutions, emulsions, suspensions, syrups, and elixirs.
- dosage forms can also contain suitable known inert diluents such as water and suitable known excipients such as preservatives, wetting agents, sweeteners, flavorants, as well as agents for emulsifying and/or suspending the compounds of the invention.
- the compounds of the present invention may be injected, for example, intravenously, in the form of an isotonic sterile solution. Other preparations are also possible.
- Suppositories for rectal administration of the compounds of the invention can be prepared by mixing the compound with a suitable excipient such as cocoa butter, salicylates and polyethylene glycols.
- Formulations for vaginal administration can be in the form of cream, gel, paste, foam, or spray formula containing, in addition to the active ingredient, such as suitable carriers, are also known.
- the pharmaceutical composition can be in the form of creams, ointments, liniments, lotions, emulsions, suspensions, gels, solutions, pastes, powders, sprays, and drops suitable for administration to the skin, eye, ear or nose. Topical administration may also involve transdermal administration via means such as transdermal patches.
- the compounds according to the invention are preferably administered by inhalation.
- lnhalable preparations include inhalable powders, propellant- containing metering aerosols or propellant-free inhalable formulations.
- inhalers for administration as a dry powder, single- or multi-dose inhalers known from the prior art may be utilized.
- the powder may be filled in gelatine, plastic or other capsules, cartridges or blister packs or in a reservoir.
- a diluent or carrier generally non-toxic and chemically inert to the compounds of the invention, e.g. lactose or any other additive suitable for improving the respirable fraction may be added to the powdered compounds of the invention.
- Inhalation aerosols containing propellant gas such as hydrofluoroalkanes may contain the compounds of the invention either in solution or in dispersed form.
- the propellant-driven formulations may also contain other ingredients such as co-solvents, stabilizers and optionally other excipients.
- the propellant-free inhalable formulations comprising the compounds of the invention may be in form of solutions or suspensions in an aqueous, alcoholic or hydroalcoholic medium and they may be delivered by jet or ultrasonic nebulizers known from the prior art or by soft-mist nebulizers such as Respimat ® .
- the compounds of the invention may be administered as the sole active agent or in combination with other pharmaceutical active ingredients including those currently used in the treatment of respiratory disorders, e.g. beta2-agonists, corticosteroids and PDE4 inhibitors.
- the dosages of the compounds of the invention depend upon a variety of factors including the particular disease to be treated, the severity of the symptoms, the route of administration, the frequency of the dosage interval, the particular compound utilized, the efficacy, toxicology profile, and pharmacokinetic profile of the compound.
- the compounds of formula (I) can be administered for example, at a dosage comprised between 0.001 and 1000 mg/day, preferably between 0.1 and 500 mg/day.
- the compounds of formula (I) are administered by inhalation route, they are preferably given at a dosage comprised between 0.001 and 500 mg/day, preferably between 0.1 and 200 mg/day.
- the compounds of formula (I) may be administered for the prevention and/or treatment of broncho-obstructive or inflammatory diseases, such as asthma, chronic bronchitis, chronic obstructive pulmonary disease (COPD), bronchial hyperreactivity, cough, emphysema or rhinitis; urological disorders such as urinary incontinence, pollakiuria, cystospasm, chronic cystitis and overactive bladder (OAB); gastrointestinal disorders such as bowel syndrome, spastic colitis, diverticulitis, peptic ulceration, gastrointestinal motility or gastric acid secretion; dry mouth; mydriasis, tachycardia; ophthalmic interventions cardiovascular disorders such as vagally induced sinus bradycardia.
- broncho-obstructive or inflammatory diseases such as asthma, chronic bronchitis, chronic obstructive pulmonary disease (COPD), bronchial hyperreactivity, cough, emphysema or rhinit
- Example 3 to 13 were obtained with a process similar to the one used to prepare compounds of Example 2, by reacting the compound prepared in Example 1 with the suitable alcohols, such as benzhydrol, fluorenol, 3-fluoro-benzol, 4-fluoro-benzol, 4-bromo- benzol, 2-hydroxy biphenyl, 2-hydroxy methyl thiophene, bis-(4-chloro- phenol) or bis-(4-bromo-phenol).
- suitable alcohols such as benzhydrol, fluorenol, 3-fluoro-benzol, 4-fluoro-benzol, 4-bromo- benzol, 2-hydroxy biphenyl, 2-hydroxy methyl thiophene, bis-(4-chloro- phenol) or bis-(4-bromo-phenol).
- the desired product is prepared by reacting imidazole-1-carboxylic acid (R)-1-aza-bicyclo[2.2.2]oct-3-yl ester with fluorenol.
- the desired product is prepared by reacting imidazole-1-carboxylic acid (R)-1-aza-bicyclo[2.2.2]oct-3-yl ester with 3-fluoro-benzol.
- the desired product is prepared by reacting imidazole-1-carboxylic acid (R)-1-aza-bicyclo[2.2.2]oct-3-yl ester with 4-fluoro-benzol.
- the desired product is prepared by reacting imidazole-1-carboxylic acid (R)-1 -aza-bicyclo[2.2.2]oct-3-yl ester with 4-bromo-benzol.
- R imidazole-1-carboxylic acid
- R 1-aza-bicyclo[2.2.2]oct-3-yl ester
- 4-bromo-benzol 4-bromo-benzol.
- EXAMPLE 8 Carbonic acid (R)-1-aza-bicyclo[2.2.2]oct-3-yl ester biphenyl-2-yl ester
- the desired product is prepared by reacting imidazole-1 -carboxylic acid (R)-1-aza-bicyclo[2.2.2]oct-3-yl ester with 2-hydroxy biphenyl.
- EXAMPLE 9 Carbonic acid (R)-1-aza-bicyclo[2.2.2]oct-3-yl ester thiophen-2- ylmethyl ester
- the desired product is prepared by reacting imidazole-1-carboxylic acid (R)-1-aza-bicyclo[2.2.2]oct-3-yl ester with 2-hydroxy methyl thiophene.
- the desired product is prepared by reacting imidazole-1-carboxylic acid (R)-1-aza-bicyclo[2.2.2]oct-3-yl ester with bis-(4-chloro-phenol).
- the desired product is prepared by reacting imidazole-1 -carboxylic acid (R)-1-aza-bicyclo[2.2.2]oct-3-yl ester with bis-(4-bromo-phenol).
- the desired product is prepared by reacting imidazole-1-carboxylic acid (R)-1-aza-bicyclo[2.2.2]oct-3-yl ester with bis-(4-fluoro-phenol).
- W NMR analysis 300 MHz, CDCI 3 -d6) ⁇ : 7.34 (m, 4H), 7.06 (m, 4H), 6.67 (s, 1 H), 4.72 (m, 1 H), 3.23 (m, 1 H), 2.83 (m, 5H), 2.08 (m, 1 H), 1.49 (m, 4H).
- the desired product is prepared by reacting imidazole-1 -carboxylic acid (R)-1 -aza-bicyclo[2.2.2]oct-3-yl ester with 3-bromo-benzol.
- the desired product is prepared by reacting 1.4 g, (3.7 mmol) of carbonic acid (R)-1-aza-bicyclo[2.2.2]oct-3-yl ester bis-(3-fluoro-phenyl)- methyl ester (obtained as described in example 2) with 2-(2- chloro)acetylthiophene (602 mg, 3.7 mmol) in EtOAc (5 ml). After stirring for 8 hours at room temperature, the solid precipitated is filtered, washed with ET.2O (2 ml) and dried under vacuum at 50 0 C.
- Example 14 The following compounds are prepared using the route described in Example 14 and in particular by reacting the compounds described in Examples 3 to 13 with 2-(2-chloro)acetylthiophene or 1-phenethyl bromide or 1-benzyl chloride or methyl iodide or 1-(3-phenoxy-propyl) bromide, as described in the following.
- the desired product is prepared by reacting carbonic acid (R)-1-aza- bicyclo[2.2.2]oct-3-yl ester benzhydryl ester with 2-(2-chloro)acetylthiophene.
- 1H NMR analysis 300 MHz, DMSO-d6) ⁇ : 2.03-1.95 (4H, m), 2.40 (1 H, s), 3.88-3.65 (5H, m), 4.19 (1 H, m), 5.13 (1 H, br s), 5.24 (2H, s), 6.74 (1 H, s), 7.45-7.30 (11 H, m), 8.16 (1 H, d), 8.22 (1 H, d).
- the desired product is prepared by reacting carbonic acid (R)-1-aza- bicyclo[2.2.2]oct-3-yl ester 9H-fluoren-9-yl ester with 2-(2- chloro)acetylthiophene.
- 1 H NMR analysis 300 MHz, DMSO-d6) ⁇ : 2.09-1.98 (4H, m), 2.50 (1 H, s), 3.78-3.69 (4H, m), 3.95 (1 H, d), 4.28 (1 H, m), 5.27-5.22 (3H, br s), 6.52 (1 H, s), 7.39-7.35 (3H, m), 7.50 (2H, d), 7.67 (2H 1 t), 7.87 (2H, d), 8.17 (1 H, d), 8.23 (1H, d).
- the desired product is prepared by reacting carbonic acid (R)-1-aza- bicyclo[2.2.2]oct-3-yl ester 3-fluoro-benzyl ester with 2-(2- chloro)acetylthiophene.
- the desired product is prepared by reacting carbonic acid (R)-1-aza- bicyclo[2.2.2]oct-3-yl ester 4-fluoro-benzyl ester with 2-(2- chloro)acetylthiophene.
- 1 H NMR analysis 300 MHz, DMSO-d6) ⁇ : 2.09-1.89 (4H, m), 2.41 (1 H, br s), 3.89-3.67 (5H, m), 4.25-4.18 (1 H 1 m), 5.13 (1 H, br s), 5.18 (2H, s), 5.25 (2H, s), 7.24 (2H, t), 7.35 (1 H, t), 7.52- 7.47 (2H, m), 8.17 (1 H, d), 8.22 (1 H, d).
- the desired product is prepared by reacting carbonic acid (R)-1-aza- bicyclo[2.2.2]oct-3-yl ester 4-bromo-benzyl ester with 2-(2- chloro)acetylthiophene.
- the desired product is prepared by reacting carbonic acid (R)-1-aza- bicyclo[2.2.2]oct-3-yl ester biphenyl-2-yl ester with 2-(2- chloro)acetylthiophene.
- the desired product is prepared by reacting carbonic acid (R)-1-aza- bicyclo[2.2.2]oct-3-yl ester 9H-fluoren-9-yl ester with 1-phenethyl bromide.
- the desired product is prepared by reacting carbonic acid (R)-1 -aza- bicyclo[2.2.2]oct-3-yl ester 9H-fluoren-9-yl ester with 1 -benzyl chloride.
- the desired product is prepared by reacting carbonic acid (R)-1-aza- bicyclo[2.2.2]oct-3-yl ester 9H-fluoren-9-yl ester with methyl iodide.
- the desired product is prepared by reacting carbonic acid (R)-1-aza- bicyclo[2.2.2]oct-3-yl ester 9H-fluoren-9-yl ester with 1-(3-phenoxy-propyl) bromide.
- 1H NMR analysis 300 MHz 1 DMSO-d6) ⁇ : 2.19-1.90 (7H, m), 2.50 (1 H, s), 3.68-3.32 (6H, m), 4.05-3.96 (3H 1 m), 5.18 (1 H 1 s), 6.62 (1 H, s), 7.88-6.94 (13H, m).
- the desired product is prepared by reacting carbonic acid (R)-1-aza- bicyclo[2.2.2]oct-3-yl ester biphenyl-2-yl ester with 1-(3-phenoxy-propyl) bromide.
- the desired product is prepared by reacting carbonic acid (R)-1-aza- bicyclo[2.2.2]oct-3-yl ester biphenyl-2-yl ester with methyl iodide.
- 1H NMR analysis 300 MHz, DMSO-d6) ⁇ : 2.18-1.80 (6H, m), 2.95 (3H, s), 3.47-3.32 (4H, m), 3.84-3.75 (1 H, m), 4.98-4.96 (1 H 1 m), 5.52-7.39 (9H, m).
- the desired product is prepared by reacting carbonic acid (R)-1-aza- bicyclo[2.2.2]oct-3-yl ester thiophen-2-ylmethyl ester with 2-(2- chloro)acetylthiophene.
- W NMR analysis 300 MHz, DMSO-d6) ⁇ : 2.10-1.95 (4H, m), 2.44 (1 H, br s), 3.87-3.66 (5H, m), 4.25-4.16 (1 H, m), 5.16 (3H, s), 5.40 (2H, s), 7.66-7.08 (4H, m), 8.15 (1 H, dd), 8.24 (1 H, dd).
- the desired product is prepared by reacting carbonic acid (R)-1 -aza- bicyclo[2.2.2]oct-3-yl ester bis-(4-chloro-phenyl)-methyl ester with 2-(2- chloro)acetylthiophene.
- the desired product is prepared by reacting carbonic acid (R)-1-aza- bicyclo[2.2.2]oct-3-yl ester bis-(4-bromo-phenyl)-methyl ester with 2-(2- chloro)acetylthiophene.
- the desired product is prepared by reacting carbonic acid (R)-1-aza- bicyclo[2.2.2]oct-3-yl ester bis-(4-fluoro-phenyl)-methyl ester with 2-(2- chloro)acetylthiophene.
- the desired product is prepared by reacting carbonic acid (R)-1-aza- bicyclo[2.2.2]oct-3-yl ester 3-bromo-benzyl ester with 2-(2- chloro)acetylthiophene.
- 1 H NMR analysis 300 MHz, DMSO-d6) ⁇ : 2.14-1.96 (4H, m), 2.45 (1 H, br s), 3.91-3.64 (5H, m), 4.26-4.19 (1H 1 m), 5.23-5.16 (5H, m), 7.59-7.37 (3H, m), 7.67-7.60 (2H, m), 8.17 (1 H, d), 8.25 (1 H, d).
- Example 33 to 42 were obtained with a process similar to the one used to prepare compound of Example 32, by reacting the compound prepared in- Example 1 with the suitable alcohols, such as bis(2-chlorophenyl)methanol, phenyl-o-tolyl-methanol, (3-fluoro- phenyl)-(3-methoxy-phenyl)-methanol, cyclohexyl-(3-fluoro-phenyl)-methanol,
- suitable alcohols such as bis(2-chlorophenyl)methanol, phenyl-o-tolyl-methanol, (3-fluoro- phenyl)-(3-methoxy-phenyl)-methanol, cyclohexyl-(3-fluoro-phenyl)-methanol,
- the desired product is prepared by reacting imidazole-1-carboxylic acid (R)-1-aza-bicyclo[2.2.2]oct-3-yl ester with bis(2-chlorophenyl)methanol.
- 1H NMR analysis 300 MHz, DMSOd 6 ) ⁇ : 7.51 - 7.63 (m, 2 H), 7.37 - 7.51 (m, 4 H), 7.22 - 7.31 (m, 2 H), 7.21 (s, 1 H), 4.53 - 4.77 (m, 1 H), 3.13 (dd, 1 H), 2.54 - 2.81 (m, 5 H), 1.88 - 2.04 (m, 1 H), 1.54 - 1.78 (m, 2 H), 1.41 - 1.54 (m, 1 H), 1.27 - 1.41 (m, 1 H).
- LC-MS (ESI POS): 406.05 (MH+).
- the desired product is prepared by reacting imidazole-1-carboxylic acid (R)-1 -aza-bicyclo[2.2.2]oct-3-yl ester with phenyl-o-tolyl-methanol.
- 1H NMR analysis 300 MHz, DMSOd 6 ) ⁇ : 7.09 - 7.51 (m, 9 H), 6.80 (s, 1 H), 4.47 - 4.79 (m, 1 H), 3.10 (dd, 1 H), 2.54 - 2.77 (m, 5 H), 2.27 (s, 3 H), 1.94 (br. s., 1 H), 1.52 - 1.76 (m, 2 H), 1.38 - 1.52 (m, 1 H), 1.16 - 1.38 (m, 1 H).
- LC-MS (ESI POS): 352.13 (MH+).
- the desired product is prepared by reacting imidazole-1-carboxylic acid (R)-1-aza-bicyclo[2.2.2]oct-3-yl ester with (3-fluoro-phenyl)-(3-methoxy- phenyl)-methanol.
- the desired product is prepared by reacting imidazole-1-carboxylic acid (R)-1-aza-bicyclo[2.2.2]oct-3-yl ester with cyclohexyl-(3-fluoro-phenyl)- methanol.
- the desired product is prepared by reacting imidazole-1-carboxylic acid (R)-1-aza-bicyclo[2.2.2]oct-3-yl ester with (3-chloro-phenyl)-(3-fluoro- phenyl)-methanol.
- m NMR analysis 300 MHz, DMSO-d ⁇ ) ⁇ : 7.50 - 7.56 (m, 1 H) 7.35 - 7.49 (m, 4 H) 7.25 - 7.35 (m, 2 H) 7.08 -
- the desired product is prepared by reacting imidazole-1 -carboxylic acid (R)-1 -aza-bicyclo[2.2.2]oct-3-yl ester with (3,5-difluoro-phenyl)-(3-fluoro- phenyl)-methanol.
- the desired product is prepared by reacting imidazole-1-carboxylic acid (R)-1-aza-bicyclo[2.2.2]oct-3-yl ester with (3-fluoro-phenyl)-m-tolyl- methanol.
- m NMR analysis 300 MHz, DMSO- ⁇ fc) ⁇ : 7.36 - 7.49 (m, 1 H), 7.06 - 7.32 (m, 7 H), 6.64 (s, 1 H), 4.32 - 4.80 (m, 1 H), 3.10 (dd, 1 H) 1 2.54 - 2.77 (m, 5 H), 2.30 (s, 3 H) 1 1.87 - 2.04 (m, 1 H), 1.11 - 1.76 (m, 4 H).
- the desired product is prepared by reacting imidazole-1 -carboxylic acid (R)-1 -aza-bicyclo[2.2.2]oct-3-yl ester with (3-fluoro-phenyl)-(4- methylsulfanyl-phenyl)-methanol.
- the desired product is prepared by reacting imidazole-1-carboxylic acid (R)-1-aza-bicyclo[2.2.2]oct-3-yl ester with (3-fluoro-phenyl)-(4-fluoro- phenyl)-methanol.
- m NMR analysis 300 MHz, DMSO-cfe) ⁇ : 7.36 - 7.56 (m, 3 H), 7.03 - 7.32 (m, 5 H), 6.72 (s, 1 H), 4.64 (ddd, 1
- the desired product is prepared by reacting imidazole-1-carboxylic acid (R)-1-aza-bicyclo[2.2.2]oct-3-yl ester with (3,4-difluoro-phenyl)-phenyl- methanol.
- the desired product is prepared by reacting imidazole-1-carboxylic acid (R)-1-aza-bicyclo[2.2.2]oct-3-yl ester with (3-fluoro-phenyl)-phenyl- methanol.
- Example 14 The following compounds are prepared using the route described in Example 14 and in particular by reacting the compound described in Example 2 with 2-bromo-1-phenyl-ethanone, 2-bromo-acetamide, 2-bromo-1- p-tolyl-ethanone, 2-bromo-1 -(4-fluoro-phenyl)-ethanone, 2-bromo-1 -(4- methoxy-phenyl)-ethanone, 2-bromo-1-thiophen-3-yl-ethanone, 2-bromo-N- phenyl-acetamide, 2-bromo-1-(5-chloro-thiophen-2-yl)-ethanone, 2-bromo-1- (3,5-dibromo-thiophen-2-yl)-ethanone, 2-bromo-1 -thiazol-2-yl-ethanone, 2- bromo-1 -o-tolyl-ethanone, 2-bromo-1 -m-tolyl-ethanone
- the desired product is prepared by reacting (R)-1-aza- bicyclo[2.2.2]oct-3-yl ester bis-(3-fluoro-phenyl)-methyl ester with 2-bromo-1- phenyl-ethanone.
- the desired product is prepared by reacting (R)-1-aza- bicyclo[2.2.2]oct-3-yl ester bis-(3-fluoro-phenyl)-methyl ester with 2-bromo- acetamide.
- the desired product is prepared by reacting (R)-1-aza- bicyclo[2.2.2]oct-3-yl ester bis-(3-fluoro-phenyl)-methyl ester with 2-bromo-1- p-tolyl-ethanone.
- the desired product is prepared by reacting (R)-1 -aza- bicyclo[2.2.2]oct-3-yl ester bis-(3-fluoro-phenyl)-methyl ester with 2-bromo-1- (4-fluoro-phenyl)-ethanone.
- the desired product is prepared by reacting (R)-1 -aza- bicyclo[2.2.2]oct-3-yl ester bis-(3-fluoro-phenyl)-methyl ester with 2-bromo-1 - (4-methoxy-phenyl)-ethanone.
- the desired product is prepared by reacting (R)-1-aza- bicyclo[2.2.2]oct-3-yl ester bis-(3-fluoro-phenyl)-methyl ester with 2-bromo-1- thiophen-3-yl-ethanone.
- the desired product is prepared by reacting (R)-1 -aza- bicyclo[2.2.2]oct-3-yl ester bis-(3-fluoro-phenyl)-methyl ester with 2-bromo-N- phenyl-acetamide.
- the desired product is prepared by reacting (R)-1-aza- bicyclo[2.2.2]oct-3-yl ester bis-(3-fluoro-phenyl)-methyl ester with 2-bromo-1- (5-chloro-thiophen-2-yl)-ethanone.
- the desired product is prepared by reacting (R)-1-aza- bicyclo[2.2.2]oct-3-yl ester bis-(3-fluoro-phenyl)-methyl ester with 2-bromo-1- (3,5-dibromo-thiophen-2-yl)-ethanone.
- the desired product is prepared by reacting (R)-1-aza- bicyclo[2.2.2]oct-3-yl ester bis-(3-fluoro-phenyl)-methyl ester with 2-bromo-1- thiazol-2-yl-ethanone.
- the desired product is prepared by reacting (R)-1-aza- bicyclo[2.2.2]oct-3-yl ester bis-(3-fluoro-phenyl)-methyl ester with 2-bromo-1- o-tolyl-ethanone.
- the desired product is prepared by reacting (R)-1-aza- bicyclo[2.2.2]oct-3-yl ester bis-(3-fluoro-phenyl)-methyl ester with 2-bromo-1- m-tolyl-ethanone.
- the desired product is prepared by reacting (R)-1-aza- bicyclo[2.2.2]oct-3-yl ester bis-(3-fluoro-phenyl)-methyl ester with 5-bromo-2- methylpent-2-ene.
- the desired product is prepared by reacting (R)-1 -aza- bicyclo[2.2.2]oct-3-yl ester bis-(3-fluoro-phenyl)-methyl ester with 1- benzo[b]thiophen-2-yl-2-bromo-ethanone.
- the desired product is prepared by reacting (R)-1 -aza- bicyclo[2.2.2]oct-3-yl ester bis-(3-fluoro-phenyl)-methyl ester with bromomethyl-benzene.
- the desired product is prepared by reacting (R)-1-aza- bicyclo[2.2.2]oct-3-yl ester bis-(3-fluoro-phenyl)-methyl ester with (2-bromoethoxy)benzene.
- the desired product is prepared by reacting (R)-1-aza- bicyclo[2.2.2]oct-3-yl ester bis-(3-fluoro-phenyl)-methyl ester with methyl iodide.
- N,N-Diisopropylethylamine (0.037 mL, 0.22 mmol) is added to a solution of 2-bromo-1-(pyridin-4-yl)ethanone hydrobromide (60.2 mg, 0.22 mmol) dissolved in EtOAc (0.5 mL). After 10 minutes, a solution of (R)-bis(3- fluorophenyl)methyl quinuclidin-3-yl carbonate (80 mg, 0.22 mmol), obtained as described in example 2, in EtOAc (0.5 mL) is added and the reaction mixture is stirred at room temperature for 2 h. Et2 ⁇ (1 mL) is added and the precipitate is collected by suction filtration. The solid is dissolved in water and extracted with DCM. The organic phase is dried over anhydrous sodium sulphate, filtered and the solvent is evaporated under reduced pressure to give the desired compound as a pink solid (76 mg; 62% yield).
- the desired product is prepared by reacting carbonic acid (R)-(I -aza- bicyclo[2.2.2]oct-3-yl) ester (3-fluoro-phenyl)-(2-fluoro-phenyl)-methyl ester with 2-(2-chloro)acetylthiophene.
- the desired product is prepared by reacting carbonic acid (R)-(I -aza- bicyclo[2.2.2]oct-3-yl) ester bis-(2-chloro-phenyl)-methyl ester with 2-(2- chloro)acetylthiophene.
- the desired product is prepared by reacting carbonic acid (R)-(I -aza- bicyclo[2.2.2]oct-3-yl) ester phenyl-o-tolyl-methyl ester with 2-(2- chloro)acetylthiophene.
- the desired product is prepared by reacting carbonic acid (R)-(I -aza- bicyclo[2.2.2]oct-3-yl) ester (3-fluoro-phenyl)-(3-methoxy-phenyl)-methyl ester with 2-(2-chloro)acetylthiophene.
- the desired product is prepared by reacting carbonic acid (R)-(I -aza- bicyclo[2.2.2]oct-3-yI) ester cyclohexyl-(3-fluoro-phenyl)-methyl ester with 2- (2-chloro)acetylthiophene.
- the desired product is prepared by reacting carbonic acid (R)-(I -aza- bicyclo[2.2.2]oct-3-yl) ester (3-chloro-phenyl)-(3-fluoro-phenyl)-methyl ester with 2-(2-chloro)acetylthiophene.
- the desired product is prepared by reacting carbonic acid (R)-(I -aza- bicyclo[2.2.2]oct-3-yl) ester (3,5-difluoro-phenyl)-(3-fluoro-phenyl)-methyl ester with 2-(2-chloro)acetylthiophene.
- the desired product is prepared by reacting carbonic acid (R)-(I -aza- bicyclo[2.2.2]oct-3-yl) ester (3-fluoro-phenyl)-m-tolyl-methyl ester with 2-(2-chloro)acetylthiophene.
- the desired product is prepared by reacting carbonic acid (R)-(I -aza- bicyclo[2.2.2]oct-3-yl) ester (3-fluoro-phenyl)-(4-methylsulfanyl-phenyl)- methyl ester with 2-(2-chloro)acetylthiophene.
- the desired product is prepared by reacting carbonic acid (R)-(I -aza- bicyclo[2.2.2]oct-3-yl) ester (4-fluoro-phenyl)-(3-fluoro-phenyl)-methyl ester with 2-(2-chloro)acetylthiophene.
- the desired product is prepared by reacting carbonic acid (R)-(I -aza- bicyclo[2.2.2]oct-3-yl) ester (3,4-difluoro-phenyl)-phenyl-methyl ester with 2-(2-chloro)acetylthiophene.
- the desired product is prepared by reacting carbonic acid (R)-(I -aza- bicyclo[2.2.2]oct-3-yl) ester (3-fluoro-phenyl)-phenyl-methyl ester with 2-(2-chloro)acetylthiophene.
- the interaction with M3 muscarinic receptors can be estimated by the results of in vitro studies which evaluated the M3/M2 binding assays, the potency of the test compounds and the offset of the inhibitory activity produced after washout of the antagonists in isolated guinea pig trachea and by the in vivo duration of action against acetylcholine-induced bronchospasm in the guinea pig.
- the pellets obtained were finally resuspended in buffer B (75 mM Tris HCI pH 7.4, 12.5mM MgCI 2 , 0.3 mM EDTA, 1 mM EGTA, 250 mM sucrose), and aliquots were stored at - 80 0 C. The day of experiment, frozen membranes were resuspended in buffer B (75 mM Tris HCI pH 7.4, 12.5mM MgCI 2 , 0.3 mM EDTA, 1 mM EGTA, 250 mM sucrose), and aliquots were stored at - 80 0 C. The day of experiment, frozen membranes were resuspended in buffer
- the potency of the antagonist activity in isolated guinea pig trachea was investigated following a method previously described by Haddad EB et al. in Br J Pharmacol 127, 413-420, 1999, with few modifications.
- a cumulative concentration-response curve to test antagonists was constructed on preparations precontracted by carbachol, until a complete inhibition of smooth muscle tone was achieved.
- the concentration of antagonist producing a 50% reversal of carbachol-induced tonic contraction (IC50) was taken as a measure of its potency in this bioassay.
- the minimal concentration of the test compounds known to produce a maximal inhibitory effect was administered to carbachol-precontracted preparations. As soon as the tonic contraction was completely reversed, the organ bath solution was renewed and preparations were thoroughly washed with fresh Krebs solution. Carbachol (0.3 ⁇ M) was administered again (at 30 min interval between washout and next administration) during the next 4 hours.
- the inhibitory effects of the compounds of the invention were expressed as percentage of the recovery of the contracting response to carbachol.
- the percentage of recovery four hours after the washout was lower than 50%.
- inhibitory M3 activity tested on compounds 1, 2, 3, 4, 5, 6, 7, 9, 11, 12, 13, 14, 15, 17 and 18 to 48 are comprised between 0.05 and 414 nM.
- Bronchial response to intravenous acetylcholine challenge was determined before and after drug administration and changes in pulmonary resistance at several time-points were expressed as percent of inhibition of bronchospasm.
- the bronchodilator activity of the tested compounds persisted unchanged up to 24 hours after the administration.
- Plasma stability of (compound 1) In order to demonstrate that the compounds are degraded, stability in rat and human plasma at 1 and 5 hours was tested for a representative compound of the invention, which is compound 1. Briefly 10 ⁇ l of a stock solution 250 ⁇ M of compound 1 in acetonitrile were added to 1 ml of rat and human plasma and samples were incubated at 37°C. Plasma (50 ⁇ L) was taken after 0, 1 and 5 hours of incubation and added to 140 ⁇ l of acetonitrile with addition of verapamil as internal standard (250 ng/ml). Samples were analysed by HPLC-MS/MS analysis.
- Plasma stability is calculated as percentage remaining after 1 and 5 hours by dividing the peak area at 1 or 5 hours by the area of the peak at time 0. After 1 and 5 hours of incubation, less than 2% of compound 1 was detected, indicating that compound 1 is very unstable in both plasma species.
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RS20120262A RS52370B (en) | 2008-08-08 | 2009-07-21 | Quinuclidine carbonate derivatives and medicinal composition thereof |
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AT09777321T ATE551341T1 (en) | 2008-08-08 | 2009-07-21 | QUINUCLIDINE CARBONATE DERIVATIVES AND MEDICAL COMPOSITION THEREOF |
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WO2011131663A1 (en) | 2010-04-21 | 2011-10-27 | Chiesi Farmaceutici S.P.A. | "process for providing particles with reduced electrostatic charges" |
US20120082727A1 (en) * | 2010-09-30 | 2012-04-05 | Chiesi Farmaceutici S.P.A. | Use of magnesium stearate in dry powder formulations for inhalation |
WO2012052297A1 (en) * | 2010-10-20 | 2012-04-26 | Chiesi Farmaceutici S.P.A. | Carbonate derivatives for the treatment of cough |
WO2012146515A1 (en) | 2011-04-29 | 2012-11-01 | Chiesi Farmaceutici S.P.A. | Alkaloid ester and carbamate derivatives and medicinal compositions thereof |
WO2013098145A1 (en) | 2011-12-30 | 2013-07-04 | Chiesi Farmaceutici S.P.A. | Quinuclidine esters of 1-azaheterocyclylacetic acid as antimuscarinic agents, process for their preparation and medicinal compositions thereof |
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WO2015052169A1 (en) | 2013-10-10 | 2015-04-16 | Chiesi Farmaceutici S.P.A. | Process for preparing pharmaceutical formulations for inhalation comprising a high-dosage strength active ingredient |
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EP2154136A1 (en) | 2008-08-08 | 2010-02-17 | CHIESI FARMACEUTICI S.p.A. | Quinuclidine carbonate derivatives and medicinal compositions thereof |
EP2206712A1 (en) | 2008-12-23 | 2010-07-14 | CHIESI FARMACEUTICI S.p.A. | "Alkaloid aminoester derivatives and medicinal composition thereof" |
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EP2206712A1 (en) | 2008-12-23 | 2010-07-14 | CHIESI FARMACEUTICI S.p.A. | "Alkaloid aminoester derivatives and medicinal composition thereof" |
BR112012032330A2 (en) | 2010-06-22 | 2016-11-08 | Chiesi Farma Spa | Inhalable dry powder formulation, use of a dry powder formulation, dry powder inhaler and packaging |
BR112013009138A2 (en) | 2010-10-20 | 2016-07-26 | Chiesi Farma Spa | compound, uses of a compound, pharmaceutical composition, inhalation device and component kit |
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- 2009-07-21 CN CN200980130187.4A patent/CN102112474B/en active Active
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- 2009-07-21 UA UAA201101383A patent/UA102857C2/en unknown
- 2009-07-21 ME MEP-2011-24A patent/ME01283A/en unknown
- 2009-07-21 RS RS20120262A patent/RS52370B/en unknown
- 2009-07-21 JP JP2011521454A patent/JP2011530489A/en active Pending
- 2009-07-21 EA EA201100161A patent/EA019166B1/en not_active IP Right Cessation
- 2009-07-21 KR KR1020117002974A patent/KR20110044221A/en not_active Application Discontinuation
- 2009-07-21 EP EP09777321A patent/EP2313404B1/en active Active
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- 2009-07-21 NZ NZ590987A patent/NZ590987A/en not_active IP Right Cessation
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- 2009-07-21 WO PCT/EP2009/005272 patent/WO2010015324A1/en active Application Filing
- 2009-07-21 CA CA2733380A patent/CA2733380A1/en not_active Abandoned
- 2009-07-21 PL PL09777321T patent/PL2313404T3/en unknown
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- 2011-08-26 US US13/219,109 patent/US8440690B2/en active Active
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WO2012052297A1 (en) * | 2010-10-20 | 2012-04-26 | Chiesi Farmaceutici S.P.A. | Carbonate derivatives for the treatment of cough |
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JP2014517808A (en) * | 2011-03-18 | 2014-07-24 | ジェンザイム・コーポレーション | Glucosylceramide synthase inhibitor |
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JP2017141255A (en) * | 2011-03-18 | 2017-08-17 | ジェンザイム・コーポレーション | Glucosylceramide synthase inhibitor |
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WO2012146515A1 (en) | 2011-04-29 | 2012-11-01 | Chiesi Farmaceutici S.P.A. | Alkaloid ester and carbamate derivatives and medicinal compositions thereof |
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