WO2003080626A1 - Derive de pyrimidine bicyclique et fusionne comme antagoniste des recepteurs de tachykinine - Google Patents
Derive de pyrimidine bicyclique et fusionne comme antagoniste des recepteurs de tachykinine Download PDFInfo
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- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
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Definitions
- the present invention relates to a novel condensed bicyclic pyridine derivative having a tachykinin receptor antagonistic activity, or a pharmacologically acceptable salt, hydrate or solvate thereof, and a pharmaceutical use thereof.
- Yukinkinin (substance P, neurokinin A, neurokinin B) is a general term for neuropeptides and their receptors in the body (two eurokinin 1 (NK 1), neurokinin 2 (NK 2), neurokinin It is known that various biological activities are expressed by binding to NK3 (NK3)).
- substance P acts as a transmitter of the central and peripheral primary sensory neurons, and also enhances diuresis, excites nerve cells, enhances blood vessel permeability, expands blood vessels, contracts smooth muscle, and immunizes. It is considered to be deeply involved in various pathological conditions (frequent urination, urinary incontinence, vomiting, inflammation, allergy, airway disease, pain, central nervous system disease, etc.). Therefore, compounds having excellent tachykinin receptor antagonism, particularly NK1 receptor antagonism, and excellent safety, long-lasting efficacy, etc. as preventive and therapeutic agents for the above various disease states The development of is desired.
- EP—A— 42 93 666 describes the formula:
- JP-A-8-67678 discloses the formula
- Y represents a nitrogen atom or an oxygen atom which may be alkylated or acylated
- R 1 represents a hydrogen atom, a lower alkyl group, a lower alkanoyl group, an alkyl group containing a nitrogen atom, a carbamoyl group, a lower An alkylthio group, a lower alkylsulfenyl group, a lower alkylsulfonyl group, a (4-phenylpiperazin-1-yl) methyl group
- R 2 is a hydrogen atom, a lower alkyl group, a lower alkyl group containing a hydroxyl group, a lower alkanol group, or a lower group.
- a ring and B ring represent a benzene ring which may have a substituent.).
- Japanese Patent Application Laid-Open No. 9-2636587 discloses a formula:
- X is a nitrogen atom or a CH group
- R 1 is a hydrogen atom, a lower alkyl group, an aryl group or an aralkyl group
- R 2 is a hydrogen atom or a lower alkyl group
- a benzene ring optionally having substituent (s); n represents 1 or 2.) is disclosed.
- R 1 and R 2 are the same or different and each represent a hydrogen atom or a C i Ce alkyl group;
- R 3 is a hydrogen atom, an optionally substituted C ⁇ Ce alkyl group, a luponyl group, A C i Ce alkylsulfonyl group, an optionally substituted C i Ce alkyl group, an optionally substituted arylmethyl group and an alkoxyl group;
- Is A benzene ring which may have 1 to 5 substituents (adjacent two substituents may be bonded to each other to form a ring);
- ring C represents 1 to 3 substituents And a benzene ring which may have a substituent (two adjacent substituents may be bonded to each other to form a ring). )
- R is a hydrogen atom, etc .;
- R 1 is a hydrogen atom, etc .;
- R 2 and R 2 ′ are hydrogen atoms, etc .;
- R 3 is a hydrogen atom, etc .;
- R 4 is a hydrogen atom, etc .;
- R 5 is a hydrogen atom, etc .;
- R 6 is a hydrogen atom or the like;
- X is - C (O) n (R 5) - , etc.;.
- n is an integer of 0 to 4;
- m is a compound represented by indicating one or 2) have been disclosed.
- R is a hydrogen atom, etc .; R 1 is a hydrogen atom, etc .; R 2 is a hydrogen atom, etc .; R 3 is a hydrogen atom, etc .; R 4 is a hydrogen atom, etc .; R 5 is a hydrogen atom, etc .; R 6 is a hydrogen atom.
- X is one C (O) N (R 5 ) —, etc .; n is an integer of 0 to 4; m is 1 or 2). (1 3) WO 0 07 32 7 No. 9
- R 1 is a hydrogen atom
- R 2 is a hydrogen atom
- R 3 is a hydrogen atom
- R 4 and R 4 ′ are hydrogen atoms
- R 5 is a lower alkyl group
- X represents —C (O) N (R 4 ") one or the like.
- R 1 is a hydrogen atom
- R 2 is a hydrogen atom
- R 3 is a hydrogen atom
- R 4 and R 4 ′ are hydrogen atoms
- R 5 is a lower alkyl group
- R 6 is a hydrogen atom
- N represents an integer of 0 to 2
- X represents —C (O) N ( 4 ′′) — and the like.
- An object of the present invention is to find a novel compound having an excellent antagonism against evening kinkinin receptor, in particular, a novel compound having an NK1 receptor antagonism, and to investigate various pathological conditions associated with evening kinkinin receptor (frequent urination, urinary incontinence). To prevent or treat vomiting, inflammation, allergy, respiratory tract disease, pain, central nervous system disease, etc.).
- the present inventors have the following general formula (1)
- ring A and ring B may have 1 to 3 substituents (two adjacent substituents may be bonded to each other to form a ring) It represents a benzene ring; R represents a C E ⁇ Ji 6 alkylsulfonyl group, alkylcarbonyl alkylsulfonyl group C E ⁇ 0 6, alkoxycarbonyl alkylsulfonyl group C E 1-6, or a formyl group; m is 1 or 2 N represents 2 or 3; q represents 1 or 2.)
- the fused bicyclic pyridine derivative represented by the formula (1) or a salt thereof has an excellent antagonistic effect on the tachykinin receptor (particularly NK1 receptor). It has been found that it has an excellent effect in animal experiments on dysuria, which is one of the tachykinin-mediated diseases, and has an effect on body urination.
- a ring and B ring Karaso among halogen atoms, substituted optionally alkyl group which may C 1 -C 6, optionally substituted C E ⁇ 0 6 alkoxy group respectively
- a benzene ring which may have 1 to 3 independently selected substituents (two adjacent substituents may be bonded to each other to form a ring);
- R represents a C 6 to alkylsulfonyl group, a C 6 alkylcarbonyl group,
- R is C ⁇ .
- 6 represents an alkylsulfonyl group, 6 to 6 alkylcarbonyl groups, 6 to 6 alkoxycarbonyl groups, or formyl group;
- R is an acetyl group and n is 3; the fused bicyclic pyridine derivative or a salt thereof according to the above (II),
- R is an acetyl group, n is 3, Q is 1 and the fused bicyclic pyridine derivative or a salt thereof according to the above (II),
- a tachykinin receptor antagonist comprising as an active ingredient the condensed bicyclic pyridine derivative or a salt thereof according to any of (I) to (V) above,
- NK1 receptor antagonist comprising as an active ingredient the condensed bicyclic pyridine derivative or a salt thereof according to any of (I) to (V),
- Urination including bladder dysfunction such as pollakiuria or urinary incontinence, characterized by containing the condensed bicyclic pyridine derivative or the salt thereof according to any one of (I) to (V) as an active ingredient.
- Preventive or therapeutic agent for disorders
- (X) X-ray irradiation, a chemotherapeutic agent, pregnancy, migraine characterized by containing the condensed bicyclic pyridine derivative or a salt thereof according to any of (I) ′ to (V) as an active ingredient.
- the present invention relates to a therapeutic agent for asthma, ⁇ , pain, migraine, toothache, rheumatoid arthritis, etc., characterized by containing a salt thereof as an active ingredient.
- the ring A and the ring B may have 1 to 3 substituents (two adjacent substituents may be bonded to each other to form a ring). Shows a good benzene ring.
- the substituents on ring A and ring B may be substituted on any of the substitutable positions of the ring, and the number thereof may be about 1 to 3. Further, two adjacent substituents may be bonded to each other to form a ring. Examples of the substituent on the ring A and the ring B include a halogen atom, an optionally substituted C i C alkyl group, and an optionally substituted C i C alkoxy group.
- halogen atom includes a fluorine atom, a chlorine atom, a bromine atom and an iodine atom.
- 1 to 3 hydrogen atoms include alkyl group optionally C i ⁇ C 6 optionally substituted by halogen atoms.
- alkoxy group optionally substituted C E ⁇ Ji 6 one to three alkoxy hydrogen atom good Ci ⁇ C 6 optionally substituted by halogen atom Group. More specifically, for example, methoxy, ethoxy, propoxy, isopropoxy, isobutoxy, sec-butoxy, tert-butoxy, fluoromethoxy, chloromethoxy, bromomethoxy, methoxy Groups, 1-fluoroethoxy group, 1-chloroethoxy group, 2-fluoroethoxy group, difluoromethoxy group, trifluoromethoxy group, trichloromethoxy group, 2,2,2-trifluoroethoxy group, etc. Can be
- Preferred ring A is, for example,
- R 5 , R 6 and R 7 are the same or different and represent a fluorine atom, a chlorine atom, a methyl group, an ethyl group, a trifluoromethyl group, a methoxy group, a trifluoromethoxy group, etc.
- a ring is a compound represented by the formula
- Preferred ring B is
- R represents a C i -C 6 alkylsulfonyl group, a C i -C 6 alkylcarbonyl group, a Ci Ce alkoxycarbonyl group, or a formyl group.
- C- 6 alkylsulfonyl group includes a methylsulfonyl group, an ethylsulfonyl group, a propylsulfonyl group and the like.
- Ce Ce alkylcarbonyl group examples include an acetyl group, a propionyl group, a petyryl group and the like.
- alkoxycarbonyl group of rCi Ce examples include a methoxycarbonyl group, an ethoxycarboeyl group, an isopropoxycarbonyl group, and a t-butoxycarbonyl group.
- n 1 or 2, and is preferably 1.
- n 2 or 3, and is preferably 3.
- Q represents 1 or 2, and is preferably 1.
- an inorganic acid such as hydrochloric acid, hydrobromic acid, sulfuric acid, nitric acid, and X is acetic acid, maleic acid, fumaric acid, succinic acid, lactic acid, malic acid, tartaric acid, citric acid, and methanesulfone.
- examples thereof include pharmaceutically acceptable salts with organic acids such as acid, p-toluenesulfonic acid, salicylic acid, stearic acid, and palmitic acid.
- the compounds of the present invention or salts thereof include optically active isomers, stereoisomers and rotamers in addition to the racemate.
- the compound of the present invention or a salt thereof may exist as a hydrate or a solvate.
- any of the hydrates and solvates formed by the condensed bicyclic pyridine derivative or its salt represented by 16 are all included in the scope of the present invention.
- Solvents that can form solvates include methanol, ethanol, isopropanol, acetone, ethyl acetate, methylene chloride, diisopropyl ether and the like.
- the compound of the present invention can be produced by various synthetic methods. Next, a typical production method of the compound of the present invention and a salt thereof will be described.
- the compound (a) (R 8 represents a hydroxyl group, a halogen atom, a 1-imidazolyl group, a 4-nitrophenoxy group, an imidoyloxy succinate group, an alkoxy group of C ⁇ Ce, a benzyloxy group, etc.) and a compound ( b) condensing (the ring B is the same as described above) to produce a compound (c) (the ring B is the same as described above).
- D CC dicyclohexylcarpoimide
- EDCI 3-ethyl-11- (3-dimethylaminopropyl) carbodiimide hydrochloride
- DMC dimethylimidazolinium chloride
- an alkali carbonate such as sodium hydrogencarbonate or potassium carbonate, triethylamine, diisopropylethylamine, N-methylmorpholine, diazabicyclo [5.4.0] -17-indene, pyridine, 4- Tertiary amines such as dimethylaminopyridine or 1,8-bis (dimethylamino) naphthylene can be exemplified.
- an inert solvent which does not participate in the reaction for example, N, N-dimethylformamide, N, N-dimethylacetamide, dimethyl sulfoxide, acetonitrile, tetrahydrofuran, dioxane, ethyl ether, dimethoxy Ethane, ethyl acetate, dichloromethane and the like are used.
- the condensation reaction can be carried out in one to twenty to eight.
- R 8 is a halogen atom, a 1-imidazolyl group, a 4-1-2 trophenoxy group, an imidoyloxy succinate group, a halide of a carboxylic acid, an imidazolide of a carboxylic acid, and an activity of a carboxylic acid.
- N N in the presence or absence of an organic base such as triethylamine, diisopropylethylamine, pyridine, and 4-methylaminopyridine, and an inorganic base such as sodium hydrogencarbonate and potassium carbonate.
- a solvent such as dimethylformamide, N, N-dimethylacetamide, dimethylsulfoxide, acetonitrile, tetrahydrofuran, dioxane, ethyl ether, dimethoxyethane, ethyl acetate, toluene, dichloromethane, etc.—3 at 20 to 80 It can be carried out by treating for 0 minutes to 48 hours. In the condensation reaction of this step, R 8 is C-.
- It can be carried out by treating with a solvent such as ril, tetrahydrofuran, dioxane, toluene, xylene, mesitylene, pyridine, quinoline or dichloromethane at 15 to 15 Ot for 30 minutes to 48 hours.
- a solvent such as ril, tetrahydrofuran, dioxane, toluene, xylene, mesitylene, pyridine, quinoline or dichloromethane at 15 to 15 Ot for 30 minutes to 48 hours.
- This step is a step of cyclizing compound (c) (ring B is as defined above) to produce compound (d) (ring B is as defined above).
- This step is carried out in the presence or absence of an organic base such as sodium tert-butoxide, potassium tert-butoxide or an inorganic base such as sodium hydride, potassium carbonate, sodium carbonate, cesium carbonate, and sodium acetate.
- solvents such as N-dimethylformamide, N, N-dimethylacetamide, dimethylsulfoxide, acetobenzyl, tetrahydrofuran, dioxane, toluene, xylene, mesitylene, pyridine, quinoline, and dichloromethane It can be carried out by treating at 50 for 30 minutes to 48 hours.
- compound (d) (B rings the same) and the compound (e) (A ring the same.
- Y is a halogen atom
- OS 0 2 R 9 R 9 is substituted with a halogen atom
- Al is an alkyl group of Ce
- B (R 1 Q ) 2 R 1 Q is a hydroxyl group, an alkyl group of C i Ce or an alkoxy group of C i to C 6 , or R 1
- This is a step of producing a compound (II) (wherein the ⁇ ring and the ⁇ ring are the same as described above) by a cross-coupling reaction in the presence of a transition metal catalyst such as a palladium or nickel complex.
- This reaction is preferably performed using an inert solvent that does not participate in the reaction.
- an inert solvent that does not participate in the reaction.
- N, N-dimethylformamide, N, N-dimethylacetamide, dimethylsulfoxide examples include side, acetonitrile, tetrahydrofuran, dioxane, dichloromethane, toluene, ethanol, water and the like. These solvents may be used alone or as a mixture in any ratio.
- the palladium complex used in this reaction include palladium chloride, palladium acetate, acetylacetonatoparadium, and tetrakis (triphenylphosphine) palladium.
- nickel complex used in this reaction examples include bis (acetylacetonato) nickel, bis (1,5-cyclooctadiene) nickel, and tetrakis (triphenylphosphine) nickel. These palladium or nickel complexes are used in the range of 0.01 to 1 equivalent, preferably 0.01 to 0.1 equivalent, relative to compound (d).
- ⁇ is a ligand for triphenylphosphine, tri-o-tolylphosphine, tri-2-furylphosphine, 1,2-bis (diphenylphosphino) ethane, 1,1 , 1-bis (diphenylphosphino) phenyl or 2,2'-bis (diphenylphosphino) 1-1,1'-binaphthyl.
- These ligands are used in a range of 0.2 to 5 equivalents, preferably 0.3 to 3 equivalents, based on the palladium or nickel complex.
- This reaction is preferably performed in the presence of a suitable base, for example, organic bases such as triethylamine, triptylamine, diisopropylethylamine, N-methylmorpholine, pyridine, lutidine, and collidine, sodium hydrogen carbonate, sodium carbonate, and potassium carbonate.
- organic bases such as triethylamine, triptylamine, diisopropylethylamine, N-methylmorpholine, pyridine, lutidine, and collidine
- sodium hydrogen carbonate sodium carbonate
- potassium carbonate and inorganic bases
- inorganic bases such as calcium carbonate, cesium carbonate and phosphate triphosphate. These bases are used in the range of 1 to 20 equivalents, preferably 2 to 10 equivalents, relative to compound (d).
- the cross-coupling reaction in this step can be carried out by treating with 15 to 150, preferably 50 to 12, for 30 minutes to 24 hours.
- This step is a step of producing a compound (g) (the rings A and B are the same as described above) by oxidizing the nitrogen of the pyridine ring of the compound (f) (the rings A and B are the same as described above). .
- 1 to 10 equivalents, preferably 1 to 2 equivalents of a peroxide is added to the compound (f).
- the treatment can be carried out by treating with ⁇ 20 to 80, preferably 0 to 30 for 30 minutes to 72 hours.
- solvent to be used examples include dichloromethane, toluene, ethyl acetate, dimethoxyethane, ethyl ether, dioxane, tetrahydrofuran, acetonitrile, N, N-dimethylformamide, N, N-dimethylacetamide and the like.
- compound (h) is produced by introducing Z (Z represents a halogen atom) using the N-oxide of compound (g) (the rings A and B are the same as described above) as a foothold. It is a process.
- Z represents a chlorine atom
- a chlorinating agent such as phosphorus oxychloride, piperoyl chloride, oxalyl chloride or the like is used in an amount of 1 to 20 equivalents, preferably 2 to 10 equivalents to the compound (g). It can be carried out by treating with an equivalent amount of 15 to; I 20t, preferably 80 to: L 20 for 30 minutes to 24 hours.
- a base for example, triethylamine, triptylamine, diisopropylethylamine, N-methylmorpholine, pyridine, lutidine, collidine and the like
- a solvent an inert solvent which does not participate in the reaction, for example, dichloromethane, xylene, toluene, dioxane, tetrahydrofuran and the like are used.
- compound (j) (R, A ring and B ring) is reacted with compound (i) (R is the same as described above) and compound (i) (R is the same as described above). Is the same as described above).
- compound (i) is converted to compound (h)
- 80 to 200 preferably 120 to 15 Ot in the presence or absence of a base using 1 to 20 equivalents for 30 minutes to 24 hours. can do.
- suitable bases include, for example, organic bases such as triethylamine, triptylamine, diisopropylethylamine, N-methylmorpholine, pyridine, lutidine, collidine, N, N-dimethylaniline, sodium hydrogen carbonate, and sodium carbonate.
- organic bases such as triethylamine, triptylamine, diisopropylethylamine, N-methylmorpholine, pyridine, lutidine, collidine, N, N-dimethylaniline, sodium hydrogen carbonate, and sodium carbonate.
- inorganic bases such as carbonated lime, calcium carbonate, cesium carbonate and phosphated lime.
- an inert solvent which does not participate in the reaction for example, N, N-dimethylformamide, N, N-dimethylacetamide, sulfolane, acetonitrile, tetrahydrofuran, dioxane, xylene, toluene, ethanol or Water or the like is used.
- the compound (1) of the present invention can be isolated and purified by a conventional separation means (for example, extraction, recrystallization, distillation, and mouth chromatography).
- a conventional separation means for example, extraction, recrystallization, distillation, and mouth chromatography.
- various salts can be produced by a usual method or a method analogous thereto (eg, neutralization).
- the compound of the present invention (1) or a salt thereof is a tachykinin receptor antagonist, a NK1 receptor antagonist, a preventive or therapeutic agent for dysuria including bladder dysfunction such as frequent urination and urinary incontinence, ulcerative colitis, Prevention or treatment of digestive diseases including Crohn's disease, X-ray irradiation, chemotherapeutic agents, prevention or treatment of vomiting induced by pregnancy, migraine, postoperative illness, gastrointestinal motility, or side effects of drug administration, etc.
- X-ray irradiation X-ray irradiation, chemotherapeutic agents, pregnancy, migraine, postoperative illness, prophylactic or therapeutic agent for vomiting induced by gastrointestinal hypomotility or side effects of drug administration, asthma, ⁇ , pain, migraine, toothache, It is useful as a therapeutic agent for rheumatoid arthritis and the like.
- the compound (1) of the present invention or a salt thereof can be used alone or in combination with one or more pharmaceutically acceptable auxiliaries as a pharmaceutical composition, and a pharmacologically acceptable carrier, excipient (eg, starch) , Lactose, calcium phosphate, Lubricants (for example, magnesium stearate, calcium talc, stearic acid, etc.), binders (for example, starch, crystalline cellulose, carboxymethyl cellulose, gum arabic, polypyrropyridone, alginic acid, etc.) ), Disintegrants (eg, talc, carboxymethylcellulose calcium, etc.), diluents (eg, physiological saline, aqueous solution of glucose, mannitol, lactose, etc.) and the like, and tablets and capsules in the usual manner.
- excipient eg, starch
- Lactose lactose
- calcium phosphate for example, lactose, calcium phosphate
- Lubricants
- the dose varies depending on the type of the compound (1) or its salt, the administration route, the age of the patient, the symptoms, etc., for example, the compound (1) or its salt for mammals including humans. As 0.00000 l to 300 mgZkg / day. For example, administration is performed once or several times a day.
- Lithium diisopropylamide solution in tetrahydrofuran Lithium diisopropylamide solution in tetrahydrofuran (Diisopropylamine (1.6 mL) is diluted with tetrahydrofuran (200 mL), and n-butyllithium (69.5 mL, 1.5 mo 1 hexane solution), and then adjusted by stirring at ⁇ 2 Ot for 30 minutes. ), A solution of 2-chloro-3-iodopyridine (23.8 g) in tetrahydrofuran (lO OmL) was added at 178, and the mixture was stirred for 5 hours. After bubbling carbon dioxide to the reaction solution for 1 hour, water was added and the temperature was raised to room temperature.
- the pH was adjusted to 1 by adding 2 ml of 1 ZL hydrochloric acid (200 mL), followed by extraction with ethyl tetrahydrofuran monoacetate (1 :: ⁇ ) and drying over anhydrous sodium sulfate. Ethyl acetate was added to the residue obtained by distilling off the solvent for crystallization, and the crystals were collected by filtration to give 2-chloro-41-nicotinic acid (22.7 g, 81%).
- the reaction solution was diluted with ethyl acetate, washed successively with water, a saturated aqueous solution of sodium hydrogen carbonate, a 20% aqueous solution of citric acid and a saturated saline solution, and then dried over anhydrous sodium sulfate.
- the residue obtained by distilling off the solvent was dissolved in tetrahydrofuran (8 mL), potassium i-t-butoxide (365 mg) was added under ice-cooling, and the mixture was stirred for 1 hour. The mixture was further stirred at room temperature for 1 hour.
- the reaction mixture was diluted with ethyl acetate, washed with water and saturated saline in that order, and dried over anhydrous sodium sulfate.
- reaction solution was diluted with ethyl acetate, washed with 2mo 1ZL aqueous sodium carbonate solution, and dried over anhydrous sodium sulfate.
- residue obtained by distilling off the solvent was recrystallized from isopropanol.
- the NK1 receptor antagonism of the test compound was determined from a concentration-response curve of substance P, which was pretreated with at least 3 concentrations of the test compound for 10 minutes and then applied cumulatively.
- the K b value is determined by the method of Schi Id (“Brit. J. Pharmacol.”, Vol. 14, p. 48, 1959). Table 1 shows the results.
- the composition of the Ty rode solution was as follows. N a C l; 1 3 6. 9, KC 1; 2. 7, C a C l 2 - 2 H 2 0; 2. 5, Mg C l 2 - 6H 2 0; 1. 0, N aH 2 P0 4 ⁇ 2H 2 0; 0. 4 , N aHC0 3; 1 1. 9, glueose; 1 1. 1 (mm o 1 / L) table 1
- Table 1 shows that compound (1) of the present invention or a salt thereof exhibits excellent NK1 receptor antagonistic activity.
- the 10th thoracic spinal cord was cut. Thereafter, both ureters were ligated and the kidney side was cut.
- a polyethylene catheter was inserted into the bladder stomach to make a physiological saline infusion channel and a bladder internal pressure measurement channel.
- the guinea pig was restrained in a pole man cage and left for more than 2 hours. Then, a physiological saline solution at room temperature was injected into the bladder from the bladder catheter at a flow rate of 6 mL / hr, and cystometry was performed. After the effective bladder capacity was stabilized, the test compound was intravenously administered via the jugular vein.
- Effective bladder capacity is the volume of physiological saline injected between urination and urination, and the effect of the test compound is the average value of bladder capacity 30 minutes before administration of the test compound and the average value of bladder volume every 30 minutes after administration The rate of increase was calculated, and the results are shown in Table 2.
- Table 2
- the compounds of the present invention have NK1 receptor antagonistic activity. Furthermore, the compounds of the present invention were confirmed to be more useful than the conventional compounds by the test examples described above.
- the compound of the present invention exhibited more excellent pharmacological effects. That is, the compound of the present invention shows the same pharmacological effect as that of the conventional compound TAK-637 at a smaller dose, and has a better pharmacological effect than the conventional compound TAK-637 at the same dose. It is superior to TAK-637 in maximum effect. Furthermore, the compounds of the present invention and their salts have low toxicity and are safe. Therefore, the compounds of the present invention and salts thereof have high utility as tachykinin receptor antagonists, therapeutic agents for dysuria, and the like.
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- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
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- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Neurosurgery (AREA)
- Pain & Pain Management (AREA)
- Urology & Nephrology (AREA)
- Pulmonology (AREA)
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- Hospice & Palliative Care (AREA)
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Description
Claims
Priority Applications (7)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP03712827A EP1489083B1 (en) | 2002-03-26 | 2003-03-24 | Fused bicyclic pyridine derivative as tachykinin receptor antagonist |
US10/508,783 US7026309B2 (en) | 2002-03-26 | 2003-03-24 | Fused bicyclic pyridine derivative as tachykinin receptor antagonist |
CA002479279A CA2479279A1 (en) | 2002-03-26 | 2003-03-24 | Fused bicyclic pyridine derivative as tachykinin receptor antagonist |
JP2003578380A JPWO2003080626A1 (ja) | 2002-03-26 | 2003-03-24 | タキキニン受容体拮抗剤としての縮合二環式ピリジン誘導体 |
KR10-2004-7015289A KR20040099367A (ko) | 2002-03-26 | 2003-03-24 | 타키키닌 수용체 길항제로서의 축합 바이사이클릭 피리딘 유도체 |
AU2003221204A AU2003221204B2 (en) | 2002-03-26 | 2003-03-24 | Fused bicyclic pyridine derivative as tachykinin receptor antagonist |
DE60314238T DE60314238T2 (de) | 2002-03-26 | 2003-03-24 | Kondensierte, bicyclische pyridinderivate als antagonisten des tachykininrezeptors |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2002-084758 | 2002-03-26 | ||
JP2002084758 | 2002-03-26 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2003080626A1 true WO2003080626A1 (fr) | 2003-10-02 |
Family
ID=28449222
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/JP2003/003487 WO2003080626A1 (fr) | 2002-03-26 | 2003-03-24 | Derive de pyrimidine bicyclique et fusionne comme antagoniste des recepteurs de tachykinine |
Country Status (9)
Country | Link |
---|---|
US (1) | US7026309B2 (ja) |
EP (1) | EP1489083B1 (ja) |
JP (1) | JPWO2003080626A1 (ja) |
KR (1) | KR20040099367A (ja) |
CN (1) | CN1310922C (ja) |
AU (1) | AU2003221204B2 (ja) |
CA (1) | CA2479279A1 (ja) |
DE (1) | DE60314238T2 (ja) |
WO (1) | WO2003080626A1 (ja) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP2158910A1 (en) * | 2003-10-27 | 2010-03-03 | Novartis Ag | Use of neurokinin antagonists in the treatment of urinary incontinence |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP5361733B2 (ja) * | 2007-11-15 | 2013-12-04 | 武田薬品工業株式会社 | ピリドオキサゼピン誘導体およびその用途 |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0652218A1 (en) * | 1993-11-10 | 1995-05-10 | Takeda Chemical Industries, Ltd. | Heterocyclic compounds, their production and use |
WO1997024356A1 (en) * | 1995-12-27 | 1997-07-10 | Janssen Pharmaceutica N.V. | 1-(1,2-disubstituted piperidinyl)-4-(fused imidazole)-piperidine derivatives |
US6147071A (en) * | 1995-03-24 | 2000-11-14 | Takeda Chemical Industries, Ltd. | Cyclic compounds, their production and use |
-
2003
- 2003-03-24 AU AU2003221204A patent/AU2003221204B2/en not_active Ceased
- 2003-03-24 EP EP03712827A patent/EP1489083B1/en not_active Expired - Lifetime
- 2003-03-24 KR KR10-2004-7015289A patent/KR20040099367A/ko not_active Application Discontinuation
- 2003-03-24 DE DE60314238T patent/DE60314238T2/de not_active Expired - Fee Related
- 2003-03-24 US US10/508,783 patent/US7026309B2/en not_active Expired - Fee Related
- 2003-03-24 WO PCT/JP2003/003487 patent/WO2003080626A1/ja active IP Right Grant
- 2003-03-24 JP JP2003578380A patent/JPWO2003080626A1/ja active Pending
- 2003-03-24 CA CA002479279A patent/CA2479279A1/en not_active Abandoned
- 2003-03-24 CN CNB038120305A patent/CN1310922C/zh not_active Expired - Fee Related
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0652218A1 (en) * | 1993-11-10 | 1995-05-10 | Takeda Chemical Industries, Ltd. | Heterocyclic compounds, their production and use |
US6147071A (en) * | 1995-03-24 | 2000-11-14 | Takeda Chemical Industries, Ltd. | Cyclic compounds, their production and use |
WO1997024356A1 (en) * | 1995-12-27 | 1997-07-10 | Janssen Pharmaceutica N.V. | 1-(1,2-disubstituted piperidinyl)-4-(fused imidazole)-piperidine derivatives |
Non-Patent Citations (1)
Title |
---|
See also references of EP1489083A4 * |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP2158910A1 (en) * | 2003-10-27 | 2010-03-03 | Novartis Ag | Use of neurokinin antagonists in the treatment of urinary incontinence |
Also Published As
Publication number | Publication date |
---|---|
US20050101591A1 (en) | 2005-05-12 |
CA2479279A1 (en) | 2003-10-02 |
AU2003221204B2 (en) | 2008-09-18 |
AU2003221204A1 (en) | 2003-10-08 |
JPWO2003080626A1 (ja) | 2005-07-21 |
US7026309B2 (en) | 2006-04-11 |
CN1656102A (zh) | 2005-08-17 |
DE60314238T2 (de) | 2008-01-31 |
DE60314238D1 (de) | 2007-07-19 |
EP1489083A1 (en) | 2004-12-22 |
CN1310922C (zh) | 2007-04-18 |
EP1489083B1 (en) | 2007-06-06 |
KR20040099367A (ko) | 2004-11-26 |
EP1489083A4 (en) | 2006-02-08 |
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