AR046269A1 - Piperidinas sustituidas, procedimiento de preparacion y uso como inhibidores potentes de renina - Google Patents
Piperidinas sustituidas, procedimiento de preparacion y uso como inhibidores potentes de reninaInfo
- Publication number
- AR046269A1 AR046269A1 ARP040103554A ARP040103554A AR046269A1 AR 046269 A1 AR046269 A1 AR 046269A1 AR P040103554 A ARP040103554 A AR P040103554A AR P040103554 A ARP040103554 A AR P040103554A AR 046269 A1 AR046269 A1 AR 046269A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- alkoxy
- oxo
- tetrazol
- benzo
- Prior art date
Links
- 239000003112 inhibitor Substances 0.000 title 1
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 34
- -1 2-oxo-dihydro-benzo- [d] [ 1,3] oxazinyl Chemical group 0.000 abstract 32
- 125000000217 alkyl group Chemical group 0.000 abstract 19
- 125000003118 aryl group Chemical group 0.000 abstract 9
- 125000003545 alkoxy group Chemical group 0.000 abstract 8
- 125000000623 heterocyclic group Chemical group 0.000 abstract 8
- 125000004432 carbon atom Chemical group C* 0.000 abstract 6
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 4
- 125000004454 (C1-C6) alkoxycarbonyl 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
- 125000004845 (C1-C6) alkylsulfonylamino group Chemical group 0.000 abstract 3
- 125000005115 alkyl carbamoyl group Chemical group 0.000 abstract 3
- 125000003806 alkyl carbonyl amino group Chemical group 0.000 abstract 3
- 125000003710 aryl alkyl group Chemical group 0.000 abstract 3
- 125000005842 heteroatom Chemical group 0.000 abstract 3
- 125000000168 pyrrolyl group Chemical group 0.000 abstract 3
- 229920006395 saturated elastomer Polymers 0.000 abstract 3
- 125000003161 (C1-C6) alkylene group Chemical group 0.000 abstract 2
- 125000006642 (C1-C6) cyanoalkyl group Chemical group 0.000 abstract 2
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 abstract 2
- 125000006577 C1-C6 hydroxyalkyl group Chemical group 0.000 abstract 2
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 2
- 125000002252 acyl group Chemical group 0.000 abstract 2
- 125000005530 alkylenedioxy group Chemical group 0.000 abstract 2
- 125000004429 atom Chemical group 0.000 abstract 2
- 125000004356 hydroxy functional group Chemical group O* 0.000 abstract 2
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 2
- 125000002971 oxazolyl group Chemical group 0.000 abstract 2
- 229910052760 oxygen Inorganic materials 0.000 abstract 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 2
- 125000000719 pyrrolidinyl group Chemical group 0.000 abstract 2
- 125000001424 substituent group Chemical group 0.000 abstract 2
- 125000003831 tetrazolyl group Chemical group 0.000 abstract 2
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 2
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 abstract 1
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 abstract 1
- 125000006590 (C2-C6) alkenylene group Chemical group 0.000 abstract 1
- 125000002152 1H-pyrrolizinyl group Chemical group C1(C=CN2C=CC=C12)* 0.000 abstract 1
- 125000002373 5 membered heterocyclic group Chemical group 0.000 abstract 1
- 125000004070 6 membered heterocyclic group Chemical group 0.000 abstract 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 abstract 1
- 239000005977 Ethylene Substances 0.000 abstract 1
- 125000003342 alkenyl group Chemical group 0.000 abstract 1
- 125000004450 alkenylene group Chemical group 0.000 abstract 1
- 125000003302 alkenyloxy group Chemical group 0.000 abstract 1
- 125000005078 alkoxycarbonylalkyl group Chemical group 0.000 abstract 1
- 125000005194 alkoxycarbonyloxy group Chemical group 0.000 abstract 1
- 125000000278 alkyl amino alkyl group Chemical group 0.000 abstract 1
- 125000005196 alkyl carbonyloxy group Chemical group 0.000 abstract 1
- 125000004656 alkyl sulfonylamino 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
- 125000004103 aminoalkyl group Chemical group 0.000 abstract 1
- 125000005160 aryl oxy alkyl group Chemical group 0.000 abstract 1
- 125000000499 benzofuranyl group Chemical group O1C(=CC2=C1C=CC=C2)* 0.000 abstract 1
- 125000005872 benzooxazolyl group Chemical group 0.000 abstract 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 1
- 229910052799 carbon Inorganic materials 0.000 abstract 1
- 125000005111 carboxyalkoxy group Chemical group 0.000 abstract 1
- 150000001875 compounds Chemical class 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
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 150000002367 halogens Chemical class 0.000 abstract 1
- 125000004415 heterocyclylalkyl group Chemical group 0.000 abstract 1
- 125000002883 imidazolyl 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
- 125000001715 oxadiazolyl group Chemical group 0.000 abstract 1
- 125000004043 oxo group Chemical group O=* 0.000 abstract 1
- 125000005476 oxopyrrolidinyl group Chemical group 0.000 abstract 1
- DHHVAGZRUROJKS-UHFFFAOYSA-N phentermine Chemical compound CC(C)(N)CC1=CC=CC=C1 DHHVAGZRUROJKS-UHFFFAOYSA-N 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
- 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
- 150000003839 salts Chemical class 0.000 abstract 1
- 229910052717 sulfur Inorganic materials 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D211/36—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D211/40—Oxygen atoms
- C07D211/42—Oxygen atoms attached in position 3 or 5
-
- 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
- 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
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Veterinary Medicine (AREA)
- Life Sciences & Earth Sciences (AREA)
- Public Health (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Urology & Nephrology (AREA)
- Ophthalmology & Optometry (AREA)
- Vascular Medicine (AREA)
- Hospice & Palliative Care (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Hydrogenated Pyridines (AREA)
Abstract
Reivindicación 1: Compuesto de fórmula (1) ó (2) en las cuales: (A) R1 en la fórmula (1) es oxazolilo, indolilo, pirrolilo, pirazolilo, triazinilo, 2-oxo-dihidro-benzo-[d][1,3]oxazinilo, 4-oxo-dihidro-imidazolilo, 5-oxo-4H-[1,2,4]triazinilo, 3-oxo- 4H-benzo[1,4]tiazinilo, tetrahidro-quinoxalinilo, 1,1,3-trioxo-dihidro-2H-1l*6*-benzo[1,4]tiazinilo, 1-oxo-piridilo, dihidro-2H-benzo[1,4]oxazinilo, 2-oxo-tetrahidro-benzo[e][1,4]diazepinilo, 2-oxo-dihidro-benzo[e][1,4]diazepinilo, 1H-pirrolizinilo, ftalazinilo, 1-oxo-3H-isobenzofuranilo, 4-oxo-3H-tieno[2,3-d]-pirimidinilo, 3-oxo-4H-benzo[1,4]oxazinilo, [1,5]naftiridilo, dihidro-2H-benzo[1,4]tiazinilo, 1,1-dioxo-dihidro-2H-benzo[1,4]tiazinilo, 2-oxo-1H-pirido[2,3-b]- [1,4]oxazinilo, dihidro-1H- pirido[2,3-b][1,4]oxazinilo, 1H-pirrolo[2,3-b]piridilo, benzo[1,3]dioxolilo, benzooxazolilo, 2-oxo-benzooxazolilo, 2-oxo-1,3-dihidro-indolilo, 2,3-dihidroindolilo, indazolilo, benzofuranilo, dihidrobenzofuranilo, tetrahidropiranilo, 2-oxo- piperidinilo o 2-oxo-azepanilo sustituidos o no sustituidos; o (B) R1 en la fórmula (1) es arilo o heterociclilo, que está sustituido con al menos un sustituyente seleccionado de alcoxi C1-6-alcoxi C1-6-alquilo C1-6, cicloalquil-C3-8-alquilo C1-6, alcoxi C1-6-carbonilo, alquilcarbonilamino C0-6, alquilcarbonilamino C0-6-alquilo C1-6, alquilcarbonilamino C0-6-alcoxi C1-6, (N-alquil C1-6)-alquilcarbonilamino C0-6-alquilo C1-6, (N-alquil C1-6)-alquilcarbonilamino-C0-6-alcoxi C1-6, cicloalquilcarbonilamino-C3-8-alquilo C1-6, cicloalquilcarbonilamino-C3-8-alcoxi C1-6, alcoxi C1-6-alquilo C1-6, hidroxialquilo C1-6, hidroxialcoxi-C1-6-alquilo C1-6, hidroxialcoxi-C1-6-alcoxi C1-6, alcoxicarbonilamino-C1-6-alquilo C1-6, alcoxicarbonilamino-C1-6-alcoxi C1-6, alquilaminocarbonilamino-C1-6-alquilo C1-6, alquilaminocarbonilamino-C1-6-alcoxi C1-6, alquilaminocarbonil-C1-6-alquilo C1-6, alquilaminocarbonil-C1-6-alcoxi C1-6, alquilaminocarbonil-C1-6-alcoxi C1-6- alquilo C1-6, di-alquilaminocarbonil-C1-6-alquilo C1-6, di-alquilaminocarbonil-C1-6-alcoxi C1-6, alquilcarboniloxi-C1-6-alquilo C1-6, alcoxicarboniloxi-C1-6-alquilo C1-6, alquilcarboniloxi-C1-6-alcoxi C1-6, ciano-alquilo C1-6, ciano-alcoxi C1-6, alcoxicarbonil-C1-6-alquilo C1-6, alcoxicarbonil-C1-6-alcoxi C1-6, alquilsulfonilamino-C1-6-alquilo C1-6, alquilsulfonilamino-C1-6 alcoxi C1-6, (N-alquil-C1-6)alquilsulfonilamino-C1-6-alquilo C1-6, (N-alquil-C1-6)-alquilsulfonilamino-C1-6-alcoxi C1- 6, aminoalquilo C1-6, aminoalcoxi C1-6, alquilamino-C1-6-alquilo C1-6, alquilamino-C1-6-alcoxi C1-6, di-alquilamino-C1-6-alquilo C1-6, di-alquilamino-C1-6-alcoxi C1-6, alquilsulfonil-C1-6-alquilo C1-6, alquilsulfonil-C1-6-alcoxi C1-6, carboxialquilo C1-6, carboxialcoxi C1-6, carboxialcoxi-C1-6-alquilo C1-6, alcoxi-C1-6-alquilcarbonilo C1-6, acilalcoxi-C1-6-alquilo C1-6, (N-alquil C1-6)-alcoxi-C1-6-carbonilamino, (N-hidroxi)-alquilaminocarbonil-C1-6-alquilo C1-6, (N-hidroxi)-alquilaminocarbonil- C1-6-alcoxi C1-6, (N-hidroxi)-aminocarbonilalquilo C1-6, (N-hidroxi)-aminocarbonilalcoxi C1-6, alcoxi-C1-6-aminocarbonilalquilo C1-6, alcoxi-C1-6-aminocarbonilalcoxi C1-6, (N-alcoxi C1-6)-alquilaminocarbonil-C1-6-alquilo C1-6, (N-alcoxi C1-6)- alquilaminocarbonil-C1-6-alcoxi C1-6, (N-acil)-alcoxi C1-6-alquilamino C1-6, alcoxi-C1-6-alquil-C1-6-carbamoilo, (N-alquil C1-6)-alcoxi C1-6-alquil C1-6-carbamoilo, alcoxi-C1-6- alquil-C1-6-carbonilo, alcoxi-C1-6-alquil-C1-6-carbonilamino, (N-alquil C1-6)-alcoxi-C1-6-alquil-C1-6-carbonilamino, carbamoil-alquilo C1-6, carbamoil-alcoxi C1-6, alquil-C1-6-carbamoilo, di-alquil-C1-6-carbamoilo, alquil-C1-6-sulfonilo, alquil C1-6- amidinilo, acetamidinil-alquilo C1-6, O-metiloximil-alquilo C1-6 y O,N- dimetilhidroxilamino-alquilo C1-6, o (C) R1 en la fórmula (1) es arilo o heterociclilo que está sustituido con al menos un sustituyente seleccionado de [1,2,4]-triazol-1-il-alquilo, [1,2,4]-triazol-1-il-alcoxi, [1,2,4]-triazol-4-il-alquilo, [1,2,4]- triazol-4-il-alcoxi, [1,2,4]-oxadiazol-5-il-alquilo, [1,2,4]-oxadiazol-5-il-alcoxi, 3-metil-[1,2,4]-oxadiazol-5-il-alquilo, 3-metil-[1,2,4]-oxadiazol-5-il-alcoxi, 5-metil-[1,2,4]-oxadiazol-3-il-alquilo, 5-metil-[1,2,4]-oxadiazol-3-il-alcoxi, tetrazol-1-il-alquilo, tetrazol-1-il-alcoxi, tetrazol-2-il-alquilo, tetrazol-2-il-alcoxi, tetrazol-5-il-alquilo, tetrazol-5-il-alcoxi, 5-metil-tetrazol-1-il-alquilo, 5-metil-tetrazol-1-il-alcoxi, tiazol-4-il-alquilo, tiazol-4-il-alcoxi, oxazol-4-il- alquilo, oxazol-4-il-alcoxi, 2-oxo-pirrolidinil-alquilo, 2-oxo-pirrolidinil-alcoxi, imidazolil-alquilo, imidazolil-alcoxi, 2-metil-imidazolil-alquilo, 2-metil-imidazolil-alcoxi, dioxolanilo, dioxanilo, ditiolanilo, ditianilo, pirrolidinilo, piperidinilo, piperazinilo, pirrolilo, 4-metilpiperazinilo, morfolinilo, tiomorfolinilo, 2-hidroximetilpirrolidinilo, 3-hidroxipirrolidinilo, 3,4-dihidroxipirrolidinilo, 3-acetamidaometilpirrolidinilo, 3-alcoxi-C1-6-alquil-C1-6-pirrolidinilo, 4- hidroxipiperidinilo, 4-oxopiperidinilo, 3,5-dimetilmorfolinilo, 4,4-dioxotiomorfolinilo, 4-oxotiomorfolinilo, 2,6-dimetilmorfolinilo, 2-oxo-imidazolidinilo, 2-oxo-oxazolidinilo, 2-oxo-pirrolidinilo, 2-oxo-[1,3]oxazinilo, 2-oxo-tetrahidro- pirimidinilo, 2-oxo-oxazolidinil-alquilo C1-6, 2-oxo-oxazolidinil-alcoxi C1-6, 1-alcoxi-alquil -C1-6-imidazol-C1-6-2-ilo, 1-alcoxi-alquil-C1-6-tetrazol-C1-6-5-ilo, 5-alcoxi-C1-6-alquil-C1-6-tetrazol-1ilo y 2-alcoxi-C1-6-alquil C1-6-4-oxoimidazol-1- ilo; o (D) R1 en la fórmula (1) es arilo o heterociclilo, cuando n es 0 y X es -O-CH-R11-CO-NR9-, o n y m son 0 y X es -O-CH-R11- y R2 es fenilo sustituido con C1-6- alcoxibenciloxi-C1-6-alcoxi; o (E) R1 en la fórmula (1) es arilo o heterociclilo, cuando n es 1 y Z es -alq-NR9- en la cual alq significa alquilen C1-6; o (F) R1 en la fórmula (1) es arilo o heterociclilo, cuando R2 significa tetrazolilo o imidazolilo, que pueden estar sustituidos con 1-3 grupos halógenos, hidroxi, ciano, trifluorometilo, alquilo C1-6, haloalquilo C1-6, hidroxialquilo C1-6, alcoxi C1-6-alquilo C1-6, cianoalquilo C1-6, carboxialquilo C1-6, alcanoiloxi-C1-6-alquilo C1-6, alcoxicarboniloxi-C1-6-alquilo C1-6, 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 (G) R1 en la fórmula (2) es arilo o heterociclilo; R2 significa 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 halógeno, hidroxi, ciano, trifluorometilo, alquilo C1-6, halo-alquilo C1-6, hidroxi-alquilo C1-6, alcoxi C1-6-alquilo C1-6,cianoalquilo C1-6, carboxialquilo C1-6, alcanoiloxi C1-6-alquilo C1-6, alcoxicarboniloxi-C1-6-alquilo C1-6, 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; L1, L2, L3, L4 y L5 significan independientemente entre sí una unión, alquileno C1-8, alquenileno C2-8 o alquinileno C2-8 o están ausentes; T1, T2, T3 y T4 significan independientemente entre sí (a) una unión o están ausentes, o un o 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 las uniones que parten de (b)-(t) llevan a un átomo de carbono aromático o saturado del grupo adyacente, cuando la unión parte de un heteroátomo, y donde no existen más de dos grupos (b)-(f), tres grupos (g)-(h) y un grupo (i)-(t); R3 es H, hidroxi, alcoxi C1-6 o alqueniloxi C1-6; R4 es H, alquilo C1-6, alquenilo C1-6, alcoxi C1-6, hidroxi- alquilo C1-6, alcoxi-C1-6-alquilo C1-6, bencilo, oxo, o un grupo R4a-Z1-X1-, donde R4a representa (a) H-, (b) alquilo C1-6, (c) alquenilo C2-6, (d) hidroxialquilo C1-6, (e) polihidroxialquilo C1-6, (f) alquil-C1-6-O-alquilo C1-6, (g) aril-, (h) heterociclil-, (i) arilalquil-, (j) heterociclilalquil-, (k) ariloxialquil-, (l) heterocicliloxialquil-, (m) (R5,R6)N-(CH2)1-3-, (n) (R5,R6)N-, (o) alquil-C1-6-S(O)0-2-, (p) aril-S(O)0-2-, (q) heterociclil-S(O)0-2-, (r) HO-SO3- o bien sus sales, (s) H2N-C(NH)-NH-, (t) NC-, y las uniones que parten de (n)-(t) y llevan hacia un átomo de C del grupo adyacente, estando éste átomo de C saturado, en caso que la unión parta de un heteroátomo; Z1 (a) representa una unión, está ausente o representa uno de los grupos, (b) alquileno C1-6, (c) alquenileno C2-6, (d) -O-, -N(R11)-, -S(O)0-2-, (e) -CO-, (f) -O-CO-, (g) -O-CO-O-, (h) -O-CO-N(R11)-, (i) -N(R11)-CO-O-, (j) -CO-N(R11)-, (k) -N(R11)-CO-, (l) -N(R11)-CO-N(R11)-, (m) -CH(OR9)-, y las uniones que parten de (d) y (f)-(m) y llevan hacia un átomo de C del grupo adyacente, estando este átomo de C saturado, en caso que la unión parta de un heteroátomo; X1 (a) representa una unión, está ausente, o uno de los grupos, (b) -O-, (c) -N(R11)-, (d) - S(O)0-2-, (e) -(CH2)1-3-, o R3 y R4 conjuntamente representan una unión; R5 y R6 significan H, alquilo C1-6, alquenilo C2-6, arilalquilo C1-6 o acilo, o conjuntamente con el átomo de N al que están unidos, significan un anillo heterocíclico de 5 o 6 miembros, que pueden contener un átomo de N, O ó S adicional o un grupo -SO- o -SO2-, donde el átomo de N adicional puede, eventualmente, estar sustituido con radicales alquilo C1-6; R7 y R8 conjuntamente con el átomo de C al que están unidos, representan un anillo de 3-7 miembros, que pueden contener uno o dos átomos de -O- o -S- o grupos -SO- o -SO2-; R9 es H, alquilo C1-6, alcoxi C1-6-alquilo C1-6, acilo o arilalquilo; R10 es carboxialquilo, alcoxicarbonilalquilo, alquilo o H; R11 es H o alquilo C1-6; R12 es H o alquilo C1-6, U significa H, alquilo C1-6, cicloalquilo C3-8, ciano, eventualmente cicloalquilo C3-8 sustituido, arilo o heterociclilo; Q significa etileno o no existe (fó
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| ARP080102063A AR066999A2 (es) | 2003-10-01 | 2008-05-15 | Piperidinas sustituidas, preparados farmaceuticos y uso como inhibidores de renina |
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| EP (2) | EP1961752A3 (es) |
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| AU2005276624B2 (en) | 2004-08-25 | 2011-09-29 | Actelion Pharmaceuticals Ltd. | Bicyclononene derivatives as renin inhibitors |
| GB0428526D0 (en) | 2004-12-30 | 2005-02-09 | Novartis Ag | Organic compounds |
| US20090270380A1 (en) * | 2005-03-31 | 2009-10-29 | Peter Herold | 3,4,5-Substituted Piperidines as Renin Inhibitors |
| 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 |
| GB0508992D0 (en) * | 2005-05-03 | 2005-06-08 | Novartis Ag | Organic compounds |
| CA2608212A1 (en) | 2005-05-27 | 2006-12-07 | Actelion Pharmaceuticals Ltd | Novel piperidine carboxylic acid amide derivatives |
| GB0514203D0 (en) * | 2005-07-11 | 2005-08-17 | Novartis Ag | Organic compounds |
| WO2007009250A1 (en) * | 2005-07-22 | 2007-01-25 | Merck Frosst Canada Ltd. | Renin inhibitors |
| RU2415840C2 (ru) * | 2005-12-30 | 2011-04-10 | Новартис Аг | 3,5-замещенные пиперидины, как ингибиторы ренина |
| EP2420491B1 (en) | 2005-12-30 | 2013-07-03 | Novartis AG | 3 , 5-substitued piperidine compounds as renin inhibitors |
| 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 |
| JP2009529033A (ja) * | 2006-03-08 | 2009-08-13 | アクテリオン ファーマシューティカルズ リミテッド | 新規アミン |
| CA2646503C (en) | 2006-04-18 | 2015-06-30 | Emisphere Technologies, Inc. | Dialkyl ether delivery agents |
| MX2008014672A (es) | 2006-05-19 | 2009-03-09 | Abbott Lab | Derivados de alcano azabiciclico sustituidos con bicicloheterociclo fusionado activos en el sistema nervioso central. |
| EP2032570A4 (en) * | 2006-06-13 | 2010-10-27 | Merck Frosst Canada Ltd | AZACYCLOPENTATE DERIVATIVES AS INHIBITORS OF STEAROYL-COENZYME-A-DELTA-9-DESATURASE |
| JP5379000B2 (ja) | 2006-07-31 | 2013-12-25 | ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ | ウロテンシンii受容体アンタゴニスト |
| 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 |
| BRPI0813900A2 (pt) | 2007-06-25 | 2014-12-30 | Novartis Ag | Derivados de n5-(2-etoxietil)-n3-(2-piridinil)-3,5-piperidinodicarboxa mida para uso como inibidores de renina |
| TW200922596A (en) | 2007-10-25 | 2009-06-01 | Speedel Experimenta Ag | 4,4-disubstituted piperidines |
| TW200932241A (en) | 2007-12-05 | 2009-08-01 | Speedel Experimenta Ag | Organic compounds |
| TW200940547A (en) * | 2007-12-13 | 2009-10-01 | Speedel Experimenta Ag | Organic compounds |
| WO2009106599A2 (en) * | 2008-02-29 | 2009-09-03 | Novartis Ag | Substituted piperidines as therapeutic compounds |
| BRPI0912388A2 (pt) | 2008-05-05 | 2017-09-26 | Merck Frosst Canada Ltd | composto, forma cristalina, processo para preparar compostos, composição farmacêutica, e, uso de um composto, e, método para o tratamento ou profilaxia de doenças |
| EP2297114B1 (en) | 2008-06-19 | 2018-06-06 | Takeda Pharmaceutical Company Limited | Heterocyclic compound and use thereof |
| ATE546448T1 (de) * | 2008-08-02 | 2012-03-15 | Janssen Pharmaceutica Nv | Urotensin-ii-rezeptorantagonisten |
| EP2358675B9 (en) | 2008-11-14 | 2019-09-11 | Theravance, Inc. | 4-[2-(2-Fluorophenoxymethyl)phenyl]piperidine compounds |
| DK2921491T3 (da) | 2011-12-27 | 2017-11-27 | Bayer Ip Gmbh | Mellemforbindelser til fremstilling af heteroarylpiperidiner og ¿piperazinderivater som fungicider |
| EP4493551A1 (en) | 2022-03-14 | 2025-01-22 | Slap Pharmaceuticals LLC | Multicyclic compounds |
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| IL123293A (en) | 1995-09-07 | 2003-06-24 | Hoffmann La Roche | Piperidine derivatives, their preparation and pharmaceutical compositions containing them |
| DE19710613A1 (de) * | 1997-03-14 | 1998-09-17 | Bayer Ag | Verfahren zur Herstellung von 5-Aminomethyl-2-chlorpyridinen |
| US6197959B1 (en) * | 1999-04-27 | 2001-03-06 | Hoffmann-La Roche Inc. | Piperidine derivatives |
| US6376672B1 (en) | 1999-04-27 | 2002-04-23 | Hoffmann-La Roche Inc. | Naphthalenylmethoxypiperidines as renin inhibitors |
| US8168616B1 (en) | 2000-11-17 | 2012-05-01 | Novartis Ag | Combination comprising a renin inhibitor and an angiotensin receptor inhibitor for hypertension |
| ES2274106T3 (es) | 2001-09-21 | 2007-05-16 | Novartis Ag | Derivados de pirano como inhibidores tanto de ace como de nep. |
| PT1517682E (pt) * | 2002-06-28 | 2007-02-28 | Speedel Pharma Ag | Formulação farmacêutica compreendendo inibidor da renina não-peptídico e tensioactivo |
| US20050020455A1 (en) * | 2003-03-04 | 2005-01-27 | Richard Mapp | Film forming and mechanical lubricant combination |
| US20040204455A1 (en) | 2003-04-10 | 2004-10-14 | Cody Wayne Livingston | Piperidine derivative rennin inhibitors |
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2004
- 2004-09-29 TW TW093129329A patent/TW200513461A/zh unknown
- 2004-09-29 TW TW097131853A patent/TW200900399A/zh unknown
- 2004-09-30 WO PCT/EP2004/052389 patent/WO2005061457A1/en not_active Ceased
- 2004-09-30 EP EP08100929A patent/EP1961752A3/en not_active Withdrawn
- 2004-09-30 US US10/574,108 patent/US7790715B2/en not_active Expired - Fee Related
- 2004-09-30 EP EP04820600A patent/EP1670760A1/en not_active Withdrawn
- 2004-09-30 AR ARP040103554A patent/AR046269A1/es not_active Application Discontinuation
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2008
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| US20070010511A1 (en) | 2007-01-11 |
| TW200513461A (en) | 2005-04-16 |
| TW200900399A (en) | 2009-01-01 |
| US7790715B2 (en) | 2010-09-07 |
| US20090012055A1 (en) | 2009-01-08 |
| WO2005061457A1 (en) | 2005-07-07 |
| AR066999A2 (es) | 2009-09-30 |
| US7842688B2 (en) | 2010-11-30 |
| EP1670760A1 (en) | 2006-06-21 |
| EP1961752A3 (en) | 2008-11-19 |
| EP1961752A2 (en) | 2008-08-27 |
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