AR053406A1 - Derivados de piperidina como inhibidores de renina. composiciones farmaceuticas - Google Patents
Derivados de piperidina como inhibidores de renina. composiciones farmaceuticasInfo
- Publication number
- AR053406A1 AR053406A1 ARP050102851A ARP050102851A AR053406A1 AR 053406 A1 AR053406 A1 AR 053406A1 AR P050102851 A ARP050102851 A AR P050102851A AR P050102851 A ARP050102851 A AR P050102851A AR 053406 A1 AR053406 A1 AR 053406A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- alkoxy
- ylalkyl
- alkoxyc
- oxo
- Prior art date
Links
- 239000008194 pharmaceutical composition Substances 0.000 title abstract 2
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical class C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 title 1
- 239000003112 inhibitor Substances 0.000 title 1
- -1 (N-hydroxy) aminocarbonyl Chemical group 0.000 abstract 41
- 125000000217 alkyl group Chemical group 0.000 abstract 37
- 125000003545 alkoxy group Chemical group 0.000 abstract 20
- 229910052739 hydrogen Inorganic materials 0.000 abstract 7
- 239000001257 hydrogen Substances 0.000 abstract 7
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 7
- 229910052757 nitrogen Inorganic materials 0.000 abstract 7
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 6
- 229910052760 oxygen Inorganic materials 0.000 abstract 6
- 125000004454 (C1-C6) alkoxycarbonyl group Chemical group 0.000 abstract 5
- 125000004457 alkyl amino carbonyl group Chemical group 0.000 abstract 5
- 125000003118 aryl group Chemical group 0.000 abstract 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 4
- 125000005115 alkyl carbamoyl group Chemical group 0.000 abstract 4
- 125000004181 carboxyalkyl group Chemical group 0.000 abstract 4
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 4
- 229910052736 halogen Inorganic materials 0.000 abstract 4
- 150000002367 halogens Chemical class 0.000 abstract 4
- 229910052717 sulfur Inorganic materials 0.000 abstract 4
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 4
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 3
- 125000003161 (C1-C6) alkylene group Chemical group 0.000 abstract 3
- 125000006642 (C1-C6) cyanoalkyl group Chemical group 0.000 abstract 3
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 abstract 3
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 abstract 3
- 125000006577 C1-C6 hydroxyalkyl group Chemical group 0.000 abstract 3
- 125000004949 alkyl amino carbonyl amino group Chemical group 0.000 abstract 3
- 125000004448 alkyl carbonyl group Chemical group 0.000 abstract 3
- 125000004432 carbon atom Chemical group C* 0.000 abstract 3
- 125000000623 heterocyclic group Chemical group 0.000 abstract 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 3
- 239000001301 oxygen Substances 0.000 abstract 3
- 125000000168 pyrrolyl group Chemical group 0.000 abstract 3
- 125000006624 (C1-C6) alkoxycarbonylamino group Chemical group 0.000 abstract 2
- 125000004890 (C1-C6) alkylamino group Chemical group 0.000 abstract 2
- 125000006625 (C3-C8) cycloalkyloxy group Chemical group 0.000 abstract 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 2
- 125000002252 acyl group Chemical group 0.000 abstract 2
- 125000005196 alkyl carbonyloxy group Chemical group 0.000 abstract 2
- 125000005530 alkylenedioxy group Chemical group 0.000 abstract 2
- 125000003710 aryl alkyl group Chemical group 0.000 abstract 2
- 125000004429 atom Chemical group 0.000 abstract 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 2
- 229910052799 carbon Inorganic materials 0.000 abstract 2
- 125000005111 carboxyalkoxy group Chemical group 0.000 abstract 2
- 125000005169 cycloalkylcarbonylamino group Chemical group 0.000 abstract 2
- 125000002883 imidazolyl group Chemical group 0.000 abstract 2
- 125000002971 oxazolyl group Chemical group 0.000 abstract 2
- 125000005476 oxopyrrolidinyl group Chemical group 0.000 abstract 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 2
- 239000011593 sulfur Substances 0.000 abstract 2
- 125000004434 sulfur atom Chemical group 0.000 abstract 2
- 125000003831 tetrazolyl group Chemical group 0.000 abstract 2
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 abstract 1
- 125000004845 (C1-C6) alkylsulfonylamino group Chemical group 0.000 abstract 1
- 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 abstract 1
- 125000006590 (C2-C6) alkenylene group Chemical group 0.000 abstract 1
- 125000006652 (C3-C12) cycloalkyl group Chemical group 0.000 abstract 1
- 125000006621 (C3-C8) cycloalkyl-(C1-C6) alkyl group Chemical group 0.000 abstract 1
- 125000006569 (C5-C6) heterocyclic group Chemical group 0.000 abstract 1
- 125000002152 1H-pyrrolizinyl group Chemical group C1(C=CN2C=CC=C12)* 0.000 abstract 1
- 125000004637 2-oxopiperidinyl group Chemical group O=C1N(CCCC1)* 0.000 abstract 1
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 1
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 abstract 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- 125000004450 alkenylene group Chemical group 0.000 abstract 1
- 125000003302 alkenyloxy group Chemical group 0.000 abstract 1
- 125000005194 alkoxycarbonyloxy group Chemical group 0.000 abstract 1
- 125000003282 alkyl amino group Chemical group 0.000 abstract 1
- 125000005093 alkyl carbonyl alkyl group Chemical group 0.000 abstract 1
- 125000003806 alkyl carbonyl amino group Chemical group 0.000 abstract 1
- 125000002947 alkylene group Chemical group 0.000 abstract 1
- 125000004419 alkynylene group Chemical group 0.000 abstract 1
- 125000002431 aminoalkoxy group Chemical group 0.000 abstract 1
- 125000005097 aminocarbonylalkyl group Chemical group 0.000 abstract 1
- 125000004104 aryloxy group Chemical group 0.000 abstract 1
- 125000005605 benzo group Chemical group 0.000 abstract 1
- 125000000499 benzofuranyl group Chemical group O1C(=CC2=C1C=CC=C2)* 0.000 abstract 1
- 125000004541 benzoxazolyl group Chemical group O1C(=NC2=C1C=CC=C2)* 0.000 abstract 1
- 125000005242 carbamoyl alkyl group Chemical group 0.000 abstract 1
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract 1
- 125000006297 carbonyl amino group Chemical group [H]N([*:2])C([*:1])=O 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 125000005159 cyanoalkoxy group Chemical group 0.000 abstract 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 abstract 1
- 125000005331 diazinyl group Chemical group N1=NC(=CC=C1)* 0.000 abstract 1
- 125000000723 dihydrobenzofuranyl group Chemical group O1C(CC2=C1C=CC=C2)* 0.000 abstract 1
- 125000000532 dioxanyl group Chemical group 0.000 abstract 1
- 125000005879 dioxolanyl group Chemical group 0.000 abstract 1
- 125000005883 dithianyl group Chemical group 0.000 abstract 1
- 125000005411 dithiolanyl group Chemical group S1SC(CC1)* 0.000 abstract 1
- 125000002541 furyl group Chemical group 0.000 abstract 1
- 125000005842 heteroatom Chemical group 0.000 abstract 1
- 125000005844 heterocyclyloxy group Chemical group 0.000 abstract 1
- 125000005113 hydroxyalkoxy group Chemical group 0.000 abstract 1
- 125000003453 indazolyl group Chemical group N1N=C(C2=C1C=CC=C2)* 0.000 abstract 1
- 125000001041 indolyl group Chemical group 0.000 abstract 1
- 125000002757 morpholinyl group Chemical group 0.000 abstract 1
- 125000001624 naphthyl group Chemical group 0.000 abstract 1
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 1
- 125000001715 oxadiazolyl group Chemical group 0.000 abstract 1
- 125000004430 oxygen atom Chemical group O* 0.000 abstract 1
- 125000004592 phthalazinyl group Chemical group C1(=NN=CC2=CC=CC=C12)* 0.000 abstract 1
- 125000004193 piperazinyl group Chemical group 0.000 abstract 1
- 125000003386 piperidinyl group Chemical group 0.000 abstract 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 1
- 125000003373 pyrazinyl group Chemical group 0.000 abstract 1
- 125000003226 pyrazolyl group Chemical group 0.000 abstract 1
- 125000004076 pyridyl group Chemical group 0.000 abstract 1
- 125000000714 pyrimidinyl group Chemical group 0.000 abstract 1
- 125000000719 pyrrolidinyl group Chemical group 0.000 abstract 1
- 229920006395 saturated elastomer Polymers 0.000 abstract 1
- 125000001424 substituent group Chemical group 0.000 abstract 1
- 125000001412 tetrahydropyranyl group Chemical group 0.000 abstract 1
- 125000000335 thiazolyl group Chemical group 0.000 abstract 1
- 125000001544 thienyl group Chemical group 0.000 abstract 1
- 125000004568 thiomorpholinyl group Chemical group 0.000 abstract 1
- 125000004306 triazinyl group Chemical group 0.000 abstract 1
- 125000001425 triazolyl group Chemical group 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/12—Drugs for disorders of the urinary system of the kidneys
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
- A61P27/06—Antiglaucoma agents or miotics
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/04—Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/12—Antihypertensives
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
Landscapes
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Urology & Nephrology (AREA)
- Ophthalmology & Optometry (AREA)
- Hospice & Palliative Care (AREA)
- Vascular Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Hydrogenated Pyridines (AREA)
Abstract
Composiciones farmacéuticas que los contienen. Reivindicacion 1: Compuesto de formula general (1), en la cual: A) R1 es arilo cuando R2 es tetrazolilo o imidazolilo, el cual puede estar sustituido con 1-3 grupos halogeno, hidroxilo, ciano, trifluorometilo, alquilo C1-6, haloalquilo C1-6, hidroxialquilo C1-6, alcoxiC1-6- alquiloC1-6, cianoalquilo C1-6, carboxialquilo C1-6, alcanoiloxiC1-6-alquiloC1-6, alcoxicarboniloxiC1-6-alquiloC1-6, alcoxicarbonilo C1-6 o alcoxi C1-6, o un grupo alquilendioxi C1-6, y/o con un radical L1-T1-L2-T2-L3-T3-L4-T4-L5-U o B) R1 es arilo cuando X es -O-CH-R11- CO-NR9-; o C) R1 es arilo cuando Z es -alq-NR9- donde alq significa alquileno C1-6, y n es 1; o D) R1 es fenilo, el cual está sustituido con 1- 4 acetamidinilalcoxi C1-6, acetamidinil-alquiloC1-6, acilalcoxiC1-6-alquiloC1-6, (N-acil)-alcoxiC1-6-alquilaminoC1-6, alcoxi C1-6, alcoxiC1-6-alcoxiC1-6, alcoxiC1-6-alcoxiC1-6-alquiloC1-6, alcoxiC1-6-alquiloC1-6, (N-alcoxiC1-6)-alquilaminocarbonilC1- 6-alcoxiC1-6, (N-alcoxiC1-6)-alquiloaminocarbonilC1-6-alquiloC1-6, alcoxiC1-6-alquilcarbamoiloC1-6, alcoxiC1-6-alquilcarboniloC1-6, alcoxiC1-6- alquilcarbonilaminoC1-6, 1-alcoxiC1-6-aquilimidazolC1-6-2-ilo, 2-alcoxiC1-6-alquilC1-6-4-oxoimidazol-1- ilo, 1-alcoxiC1-6- alquiltetrazolC1-6-5-ilo, 5-alcoxiC1-6-alquiltetrazolC1-6-1-ilo, 6-alcoxiaminocarbonilalcoxiC1-6, alcoxiaminocarbonilC1-6-alquloC1-6, alcoxicarbonilo C1-6, alcoxicarbonilC1-6-alcoxiC1-6, alcoxicarbonilC1-6-alquiloC1-6, alcoxicarbonilaminoC1-6-alcoxiC1-6, alcoxicarbonilaminoC1-6-alquiloC1-6, alquilo C1-6, (N-alquilC1-6)-alcoxiC1-6, alquilcarbamoilo C1-6, (N-alquilC1-6)-alcoxiC1-6- alquilcarbonilaminoC1-6, (N-alquilC1-6)-alcoxicarbonilaminoC1-6, (N-alquilC1-6)- alquilcarbonilaminoC0-6-alcoxiC1-6, (N-alquilC1-6)- alquil carbonilaminoC0-6-alquiloC1-6, (N-alquilC1-6)-alquilsulfonilaminoC1-6-alcoxiC1-6, (N-alquilC1-6)-alquilsulfonilaminoC1-6- alquiloC1-6, alquilamidinilo C1-6, alquilaminocarbonilC1-6-alcoxiC1-6, di-alquilaminocarbonilC1-6-alcoxiC1-6, alquilaminocarbonilC1-6- alcoxiC1-6-alquiloC1-6, alquilaminocarbonilC1-6-alquiloC1-6, alquilaminocarbonilaminoC1-6-alcoxiC1-6, alquilaminocarbonilaminoC1-6- alquiloC1-6, di-alquilaminocarbonilC1-6-alquiloC1-6, alquilaminoC1-6-alcoxiC2-6, di-alquilaminoC1-6-alcoxiC2-6, alquilaminoC1-6- alquiloC1-6, di-alquilaminoC1-6-alquiloC1-6, alquilcarbamoilo C1-6, di-alquilcarbamoiloC1-6, alquilcarbonilo C0-6, alquilcarbonilaminoC0-6alcoxicarboniloxiC1-6, alquilcarbonilamino C0-6, alquilcarbonilaminoC0-6alquiloC1-6, alquilcarboniloxiC1-6- alcoxiC1-6, alquilcarboniloxiC1-6-alquiloC1-6, alquilsulfonilo C1-6, alquilsulfonilC1-6-alcoxiC1-6, alqilsulfonilC1-6-alquiloC1-6, alquilsulfonilaminoC1-6-alcoxiC1- 6, alquilsulfonilaminoC1-6-alquiloC1-6, carbamoilo, carbamoilalcoxi C1-6. carbamoilalquilo C1-6, carboxialcoxi C1-6, carboxialcoxiC1-6-alquiloC1-6, carboxialquilo C1-6, ciano, cianoalcoxi C1-6, cianoalquilo C1-6, cicloalquilcarbonilaminoC3-6- alcoxiC1-6, cicloalquilcarbonilaminoC3-6-alquiloC1-6, ciclopropilalquilo C1-6, O,N- dimetilhidroxilaminoalquiloC1-6, haloalcoxi C1-6, haloalquilo C1-6, halogeno, hidroxialcoxiC1-6-alcoxiC1-6, hidroxialcoxiC1-6-alquiloC1-6, hidroxialquilo C1-6, (N- hidroxi)alquilaminocarboniloC1-6-alcoxiC1-6, (N-hidroxi)alquilaminocarbonilC1-6-alquiloC1-6, (N-hidroxi) aminocarbonil-alcoxiC1-6, (N-hidroxi)aminocarbonilalquiloC1-6, 2-oxooxazolidinilalcoxiC1-6, 2-oxooxazolidinilalquiloC1-6, O-metiloximil- alquiloC1- 6- o trifluorometilo; o E) R1 es arilo, el cual está sustituido con 3-acetamidometilpirrolidinilo, 3-alcoxiC1-6-alquilC1-6- pirrolidinilo, 3,4-dihidroxipirrolidinilo, 2,6-dimetilmorfolinilo, 3,5-dimetilmorfolinilo, dioxanilo, dioxolanilo, 4,4- dioxotiomorfolinilo, ditianilo, ditiolanilo, 2-hidroximetilpirrolidinilo, 4-hidroxipiperidinilo, 3-hidroxipirrolidinilo, imidazolilalcoxi, imidazolilalquilo, 2- metilimidazolilalcoxi, 2-metilmidazolilalquilo, 3-metil[1,2,4]oxadiazol-5-ilalcoxi, 5- metil[1,2,4]oxadiazol-3-ilalcoxi, 3-metil-[1,2,4]- oxadiazol-5-ilalquilo, 5-metil[1,2,4]oxadiazol-3-ilalquilo, 4-metilpiperazinilo, 5-metiltetrazol-1-ilalcoxi, 5-metiltetrazol-1-ilalquilo, morfolinilo, [1,2,4]oxadiazol-5-ilalcoxi, [1,2,4]oxadiazol-5- ilalquilo, oxazol-4-ilalcoxi, oxazol-4-ilalquilo, 2-oxo-[1,3]oxazinilo, 2- oxooxazolidinilo, 2-oxoimidazolidinilo, 2-oxopirrolidinilo, 4-oxopiperidinilo, 2-oxo-pirrolidinilalcoxi, 2-oxopirrolidinilalquilo, 2- oxotetrahidropirimidinilo, 4- oxotiomorfolinilo, piperazinilo, piperidinilo, pirrolidinilo, pirrolilo, [1,2,4]-triazol-1-ilalcoxi, [1,2,4]triazol-4- ilalcoxi, [1,2,4]triazol-1-ilalquilo, [1,2,4]triazol-4-ilalquilo, tetrazol-1-ilalcoxi, tetrazol-2-ilalcoxi, tetrazol-5-ilalcoxi, tetrazol-1-ilalquilo, tetrazol-2-ilalquilo, tetrazol-2-ilalquilo, tetrazol-5-ilalquilo, tiazol-4-ilalcoxi, tiazo-4-ilalquilo, tiomorfolinilo; o F) R1 es heterociclilo, opcionalmente sustituido, en particular como se específica en D) o E), en particular benzo[1,3]dioxoilo, benzofuranilo, benzoxazolilo, dihidrobenzofuranilo, 3,4-dihidro-2H-benzo[1,4]oxazinilo, dihidro-3H-benzo[1,4]oxazinilo, dihidro-2H-benzo[1,4]tiazinilo, 2,3- dihidroindolilo, dihidro-1H-pirido[2,3-b][1,4]oxazinilo, 1,1- dioxodihidro-2H-benzo[1,4]tiazinilo, indazolilo, indolilo, [1,5]naftiridilo, oxazolilo, 2-oxoazepanilo, 3-oxo-4H-benzo[1,4]oxazinilo, 2-oxobenzoxazolilo, 3-oxo-4H-benzo[1,4]tiazinilo, 2-oxodihidrobenzo[e][1,4]- diazepinilo, 2- oxodihidrobenzo[d][1,3]oxazinilo, 2-oxodihidro-1H-quinazolinilo, 4-oxodihidroimidazolilo, 2-oxo-1,3-dihidroindolilo, 1- oxo-3H-isobenzofuranilo, 2-oxopiperidinilo, 2-oxo-1H-pirido[2,3-b][1,4]oxazinilo, 1-oxopiridilo, 2- oxotetrahidrobenzo[e][1,4]diazepinilo, 4-oxo-3H-tieno[2,3-d]pirimidinilo, 5-oxo-4H-[1,2,4]-triazinilo, ftalazinilo, pirazolilo, 1H-pirrolizinilo, 1H-pirrolo[2,3-b]piridilo, pirrolilo, tetrahidroquinoxalinilo, tetrahidropiranilo, triazinilo, imidazo[1,5-a]piridinilo, tetrahidro-imidazo[1,5-a]piridinilo o 1,1,3- trioxodihidro-2H-1lambda6-benzo[1,4]tiazinilo; R2 es fenilo, naftilo, acenaftilo, ciclohexilo, piridilo, pirimidinilo, pirazinilo, oxopiridinilo, diazinilo, triazolilo, tienilo, oxazolilo, oxadiazolilo, tiazolilo, pirrolilo, furilo, tetrazolilo o imidazolilo, radicales que pueden estar sustituidos con 1-3 grupos halogeno, hidroxilo, ciano, trifluormetilo, alquilo C1-6, haloalquilo C1-6, hidroxialquilo C1-6, alcoxiC1-6- alquiloC1-6, cianoalquilo C1-6, carboxialquilo C1-6, alcanoiloxiC1-6-alquiloC1-6, alcoxicarboniloxiC1-6-alquiloC1-6, alcoxicarboniloC1-6, o alcoxi C1-6, o un grupo alquilendioxi C1-6, y/o con un radical L1-T1-L2-T2-L3-T3-L4-T4-L5-U; L1, L2, L3, L4 y L5 son cada uno independientemente un enlace, alquileno C1-8, alquenileno C2-8 o alquinileno C2-8, o están ausentes; T1, T2, T3 y T4 son cada uno independientemente: a) un enlace, o están ausentes o son uno de los grupos; b) -CH(OH)-; c) -CH(OR6)-; d) -CH(NR5R6)-; e) -CO-; f) -CR7R8-; g) -O- o - NR6-; h) -S(O)0-2-; i) -SO2NR6-; j) -NR6SO2-; k) -CONR6-; l) -NR6CO-; m) -O-CO-; n) -CO-O-; o) -O-CO-O-; p) -O-CO-NR6-; q) - N(R6)-CO-N(R6)-; r) -N(R6)-CO-O-; s) pirrolidinileno, piperidinileno o piperazinileno; t) -C(R11)(R12)-, donde los enlaces que comienzan en b)-t) conducen a un átomo de carbono saturado o aromático del grupo adyacente si el enlace comienza en un heteroátomo, y donde no más de dos grupos b)-f), tres grupos g)-h) y un grupo i)-t) está/n presente/s; R3 es hidrogeno, hidroxilo, alcoxi C1-6 o alqueniloxi C1-6; R4 es alcoxi C1-6, alcoxiC1-6-alcoxiC1-6, amino opcionalmente N-mono- o N,N-dialquiladoC1-6, aminoalcoxi C1-6 opcionalmente N-mono- o N,N-dialquiladoC1-6, alcoxicarbonilaminoC1-6-alcoxiC1-6 opcionalmente N-alquiladoC1-6, cicloalquilC3-8-alquilcarbonilaminoC1-6-alcoxiC1-6 o opcionalmente N-alquiladoC1-6, alquilcarbonilC1-6-alcoxiC1-6, alquilcarboniloxi C1-6, arilalcoxi C1-6, ariloxi, carbamoilalcoxi C1- 6 opcionalmente N-mono- o N,N-di-alquiladoC1-6, carbamoilalcoxi C1-6 opcionalmente N-mono- o N,N-dicicloalquilC3-8-alquiladoC1-6, carbamoiloxi opcionalmente N-mono- o N,N-di-alquiladoC1-6, cianoalquiloxi, cicloalquiloxi C3-8, cicloalquilC3-8- alcoxiC1-6, cicloalquiloxiC3-8-alcoxiC1-6, hidroxilo, hidroxialcoxi C1-6, hidroxialcoxiC1-6-alcoxiC1-6, heterociclilalcoxi C1-6, heterocicliloxi, heterocicloxialcoxi C1-6 u oxo; R5 y R6 son cada uno en forma independiente hidrogeno, alquilo C1-6, alquenilo C2-6, arilalquilo C1-6 o acilo, o junto con el átomo de N al cual están unidos, son un anillo heterocíclico de 5 a 6 miembros, el cual puede contener un átomo adicional de N, O o S o un grupo -SO- o -SO2-, donde el átomo adicional de N puede opcionalmente estar sustituido con radicales alquilo C1-6; R7 y R8, junto con el átomo de carbono al cual están unidos, son un anillo de 3 a 7 miembros, que puede contener uno o dos átomos de O o S o grupos -SO- o -SO2-; R9 es hidrogeno, alquilo C1-6, alcoxiC1-6- alquiloC1-6, acilo, arilalquilo C1-6, cicloalquilo C3-8 o cicloalquilC3-8-alquiloC1-6; R10 es carboxialquilo C1-6, alcoxicarbonilC1-6- alquiloC1-6, alquilo C1-6 o hidrogeno; R11 es hidrogeno, halogeno o alquilo C1-6; R12 es hidrogeno, halogeno o alquilo C1-6; R11 y R12, junto con el átomo de C al que están unidos, también pueden ser cicloalquilo C3-8; U es hidrogeno, alquilo C1-6, ciano, trifluormetilo, cicloalquilo C3-12 opcionalmente sustituido, arilo o heterociclilo; X es un enlace, oxígeno, nitrogeno o azufre, donde un enlace que comienza en un átomo de oxígeno, nitrogeno o azufre conduce a un átomo de C saturado del grupo Z o a R1, o es > CR11R12, >CHOR9, -O-CO-, >CO, >C=NOR10, -O-CR11R12-, -O- CR11R12-CO-NR9-, o -CO-NR9-, W es oxígeno o azufre; Z es alquileno C1-6, alquenileno C2-6, hidroxialquillideno C1-6, -O-, -N-, -S-, -O-alq-, -NR9-alq, -S-alq-, -alq-O-, -alq-S- o -alq-NR9-, en el que alq significa alquileno C1-6 y donde a) si Z es - O-, o -S-, X es -CR11R12- y/o R2 contiene un sustituyente L1-T1-L2-T2-L3-T3- L4- T4-L5-U o R4 es un sustituyente diferente de hidrogeno tal como se definio anteriormente; b) si Z es -O-alq- o
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| US (1) | US20080076766A1 (es) |
| EP (1) | EP1776359B1 (es) |
| JP (1) | JP4842262B2 (es) |
| CN (1) | CN101014594A (es) |
| AR (1) | AR053406A1 (es) |
| AT (1) | ATE521607T1 (es) |
| BR (1) | BRPI0513199A (es) |
| CA (1) | CA2570920A1 (es) |
| ES (1) | ES2372502T3 (es) |
| IL (1) | IL180242A0 (es) |
| PL (1) | PL1776359T3 (es) |
| PT (1) | PT1776359E (es) |
| TW (1) | TW200613274A (es) |
| WO (1) | WO2006005741A2 (es) |
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| JP2008510755A (ja) | 2004-08-25 | 2008-04-10 | アクテリオン ファーマシューティカルズ リミテッド | ビシクロノネン誘導体 |
| GB0428526D0 (en) | 2004-12-30 | 2005-02-09 | Novartis Ag | Organic compounds |
| EP1707202A1 (de) * | 2005-03-31 | 2006-10-04 | Speedel Experimenta AG | Organische Verbindungen |
| TW200722424A (en) * | 2005-03-31 | 2007-06-16 | Speedel Experimenta Ag | Substituted piperidines |
| BRPI0609534A2 (pt) * | 2005-03-31 | 2010-04-13 | Speedel Experimenta Ag | piperidinas 3,4,5-substituìdas |
| GB0508992D0 (en) * | 2005-05-03 | 2005-06-08 | Novartis Ag | Organic compounds |
| GB0510810D0 (en) * | 2005-05-26 | 2005-06-29 | Novartis Ag | Organic compounds |
| KR100963455B1 (ko) | 2005-05-27 | 2010-06-18 | 액테리온 파마슈티칼 리미티드 | 신규한 피페리딘 카르복실산 아미드 유도체 |
| GB0514203D0 (en) | 2005-07-11 | 2005-08-17 | Novartis Ag | Organic compounds |
| ES2430139T3 (es) | 2005-12-30 | 2013-11-19 | Novartis Ag | Compuestos de piperidina 3,5-sustituido como inhibidores de renina |
| EP1816122A3 (en) * | 2006-01-19 | 2007-09-19 | Speedel Experimenta AG | 3,4,5-substituted piperidines as therapeutic compounds |
| TW200804359A (en) * | 2006-01-19 | 2008-01-16 | Speedel Experimenta Ag | Substituted 4-phenylpiperidines |
| TW200821303A (en) * | 2006-08-08 | 2008-05-16 | Speedel Experimenta Ag | Organic compounds |
| EP1911758A1 (en) * | 2006-10-04 | 2008-04-16 | Speedel Experimenta AG | Phenyl piperidine derivatives for use as renin inhibitors |
| EP1908761A1 (en) * | 2006-10-04 | 2008-04-09 | Speedel Experimenta AG | Organic compounds |
| WO2008074450A2 (en) * | 2006-12-20 | 2008-06-26 | Nicox S.A. | Non-peptidic renin inhibitors nitroderivatives |
| TWI452044B (zh) * | 2007-06-15 | 2014-09-11 | Mitsubishi Tanabe Pharma Corp | 嗎啉衍生物 |
| EP2181105B1 (en) | 2007-06-25 | 2015-04-29 | Novartis AG | N5-(2-ethoxyethyl)-n3-(2-pyridinyl)-3,5-piperidinedicarboxamide derivatives for use as renin inhibitors |
| AR069005A1 (es) * | 2007-10-25 | 2009-12-23 | Speedel Experimenta Ag | Piperidinas 4,4-disustituidas |
| TW200932241A (en) * | 2007-12-05 | 2009-08-01 | Speedel Experimenta Ag | Organic compounds |
| JP2011511038A (ja) | 2008-02-08 | 2011-04-07 | ノバルティス アーゲー | レニン阻害剤としての置換ピペリジン |
| EA201001239A1 (ru) | 2008-02-08 | 2011-04-29 | Новартис Аг | Замещённые пиперидины в качестве ингибиторов ренина |
| WO2009106599A2 (en) * | 2008-02-29 | 2009-09-03 | Novartis Ag | Substituted piperidines as therapeutic compounds |
| WO2009127251A1 (en) * | 2008-04-16 | 2009-10-22 | Novartis Ag | Combinations comprising a renin inhibitor |
| CN102015682B (zh) * | 2008-05-05 | 2014-07-16 | 埃科特莱茵药品有限公司 | 作为肾素抑制剂的3,4-取代的哌啶衍生物 |
| PE20110067A1 (es) | 2008-06-19 | 2011-02-18 | Takeda Pharmaceutical | Derivados de piperidina como inhibidores de renina |
| EP2163245A1 (en) | 2008-09-10 | 2010-03-17 | Novartis Ag | Renin inhibitors for the treatment of psoriasis |
| US8592454B2 (en) | 2008-09-19 | 2013-11-26 | Takeda Pharmaceutical Company Limited | Nitrogen-containing heterocyclic compound and use of same |
| US20120035214A1 (en) * | 2009-04-03 | 2012-02-09 | Merck Canada Inc. | Renin inhibitors |
| EP2384745A3 (en) * | 2010-05-05 | 2012-01-18 | Sanovel Ilac Sanayi ve Ticaret A.S. | Modified release pharmaceutical compositions of dexlansoprazole |
| EP2384746A3 (en) | 2010-05-05 | 2012-03-07 | Sanovel Ilac Sanayi ve Ticaret A.S. | Dual release oral tablet compositions of dexlansoprazole |
| US8563035B2 (en) | 2010-05-05 | 2013-10-22 | Sanovel Ilac Sanayi Ve Ticaret Anomin Sirketi | Oral tablet compositions of dexlansoprazole |
| EP4255909A1 (en) * | 2020-12-02 | 2023-10-11 | Qurient Co. Ltd. | Compounds having cyclin-dependent kinase(cdk)-inhibitory function |
| JP2025510646A (ja) | 2022-03-14 | 2025-04-15 | スラップ ファーマシューティカルズ エルエルシー | 多環式化合物 |
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| KR100384979B1 (ko) * | 1995-09-07 | 2003-10-17 | 에프. 호프만-라 로슈 아게 | 심부전증및신부전증치료용의신규한4-(옥시알콕시페닐)-3-옥시-피페리딘 |
| US6376672B1 (en) * | 1999-04-27 | 2002-04-23 | Hoffmann-La Roche Inc. | Naphthalenylmethoxypiperidines as renin inhibitors |
| US6197959B1 (en) * | 1999-04-27 | 2001-03-06 | Hoffmann-La Roche Inc. | Piperidine derivatives |
| US20030095958A1 (en) * | 2001-04-27 | 2003-05-22 | Bhisetti Govinda R. | Inhibitors of bace |
| US20040204455A1 (en) * | 2003-04-10 | 2004-10-14 | Cody Wayne Livingston | Piperidine derivative rennin inhibitors |
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Also Published As
| Publication number | Publication date |
|---|---|
| CA2570920A1 (en) | 2006-01-19 |
| EP1776359A2 (en) | 2007-04-25 |
| PL1776359T3 (pl) | 2012-01-31 |
| ES2372502T3 (es) | 2012-01-20 |
| JP4842262B2 (ja) | 2011-12-21 |
| EP1776359B1 (en) | 2011-08-24 |
| CN101014594A (zh) | 2007-08-08 |
| JP2008505871A (ja) | 2008-02-28 |
| BRPI0513199A (pt) | 2008-04-29 |
| HK1104037A1 (en) | 2008-01-04 |
| WO2006005741A3 (en) | 2006-07-06 |
| PT1776359E (pt) | 2011-12-15 |
| TW200613274A (en) | 2006-05-01 |
| WO2006005741A2 (en) | 2006-01-19 |
| ATE521607T1 (de) | 2011-09-15 |
| IL180242A0 (en) | 2007-07-04 |
| US20080076766A1 (en) | 2008-03-27 |
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