AR048320A1 - Derivados de 5-amino-4-hidroxi-7-(1h-indolilmetil)-8-metilnonanamida - Google Patents
Derivados de 5-amino-4-hidroxi-7-(1h-indolilmetil)-8-metilnonanamidaInfo
- Publication number
- AR048320A1 AR048320A1 ARP050101073A ARP050101073A AR048320A1 AR 048320 A1 AR048320 A1 AR 048320A1 AR P050101073 A ARP050101073 A AR P050101073A AR P050101073 A ARP050101073 A AR P050101073A AR 048320 A1 AR048320 A1 AR 048320A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- alkoxy
- oxo
- amino
- pyrimidinyl
- Prior art date
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Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C237/00—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups
- C07C237/02—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atoms of the carboxamide groups bound to acyclic carbon atoms of the carbon skeleton
- C07C237/04—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atoms of the carboxamide groups bound to acyclic carbon atoms of the carbon skeleton the carbon skeleton being acyclic and saturated
- C07C237/06—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atoms of the carboxamide groups bound to acyclic carbon atoms of the carbon skeleton the carbon skeleton being acyclic and saturated having the nitrogen atoms of the carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
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- 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
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- 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
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
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- 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
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- 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
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- 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
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- 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
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C237/00—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups
- C07C237/02—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atoms of the carboxamide groups bound to acyclic carbon atoms of the carbon skeleton
- C07C237/22—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atoms of the carboxamide groups bound to acyclic carbon atoms of the carbon skeleton having nitrogen atoms of amino groups bound to the carbon skeleton of the acid part, further acylated
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/10—Indoles; Hydrogenated indoles with substituted hydrocarbon radicals attached to carbon atoms of the hetero ring
- C07D209/12—Radicals substituted by oxygen atoms
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/54—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings condensed with carbocyclic rings or ring systems
- C07D231/56—Benzopyrazoles; Hydrogenated benzopyrazoles
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- 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
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Urology & Nephrology (AREA)
- Ophthalmology & Optometry (AREA)
- Vascular Medicine (AREA)
- Hospice & Palliative Care (AREA)
- Virology (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Indole Compounds (AREA)
Abstract
Proceso para su preparacion y uso de estos compuestos como medicamentos, especialmente como inhibidores de renina. Reivindicacion 1: Compuestos de la formula general en la cual: X es -CH2- o >CH-OH; A) R1 es un radical heterociclilo opcionalmente sustituido o un radical hidrocarbonado no saturado policíclico opcionalmente sustituido cuando X es hidroximetileno; o B) R1 es un radical heterociclilo o un radical hidrocarbonado no saturado policíclico que está sustituido con de uno a cuatro radicales seleccionados de alquilo C1-6, cicloalquilo C3-8, cicloalcoxilo C3-8, cicloalcoxiC3-8-alquiloC1-6, cicloalcoxiC3-6-alcoxiloC1-6, alquilC1-6-amino, dialquilC1-6-amino, amino-alquiloC1-6, amino-alcoxiloC2-7, polihaloalquilo C1-6, polihaloalcoxilo C2-7, nitro, amino, alquenilo C2-6, alcoxilo C1-6, alcanoiloxi C1-6, hidroxilo, halogeno, ciano, carbamoilo, carboxilo y alquilenC1-6-dioxilo, fenilo, fenoxilo, fenilo, fenil-alquiloC1-6 o fenil-alcoxiloC1-6 opcionalmente sustituido con halogeno, alquilo C1-6, alcoxilo C1-6, hidroxilo, alquilC1-6-amino, dialquilC1-6-amino, alcoxiC1-6-carbonilo, hidroxi-alquiloC1-6 o trifluorometilo, piridilcarbonilamino-alquiloC1-6, alqueniloxilo C2-7, alcoxiC1-6-alcoxiloC1-6, alcoxiC1-6-alcoxi- C1-6-alquiloC1-6, metoxibenciloxilo, hidroxibenciloxilo, metilendioxibenciloxilo, dioxolanil-alcoxiloC1-6, cicloalquilC3-6-alquiloC1-6, cicloalquilC3-8-alcoxiloC1-6, hidroxi-alcoxiloC2-7, carbamoiloxi-alcoxiloC2-7, piridilcarbamoiloxi-alcoxiloC2-7, benzoiloxi-alcoxiloC2-7, alcoxiC1-6-carbonilo, alquilC1-6-carbonilamino, alquilC1-6-carbonilamino-alquiloC1-6, alquilC1-6-carbonilamino-alcoxiloC2-7, (N-alquilC1-6)-alquilC1-6-carbonilamino-alquiloC1-6, (N-alquilC1-6)-alquilC1-6-carbonilamino- alcoxiloC2-7, cicloalquilC3-8-carbonilamino-alquiloC1-6, cicloalquilC3-8-carbonilamino-alcoxiloC2-7, alcoxiC1-6-alquiloC1-6, hidroxi-alquiloC1-6, hidroxi-alcoxiC2-7-alquiloC1-6, hidroxi-alcoxiC1-6-alcoxiloC1-6, alcoxiC1-6-carbonilamino-alquiloC1-6, alcoxiC1-6-carbonil-amino-alcoxiloC2-7, alquilC1-6-aminocarbonilamino-alquiloC1-6, alquilC1-6-aminocarbonilamino-alcoxiloC2-7, alquilC1-6-aminocarbonil-alquiloC1-6, alquilC1-6-aminocarbonil-alcoxiloC1-6, alquilC1-6-aminocarbonil-alcoxiC1-6-alquiloC1- 6, dialquilC1-6-aminocarbonil-alquiloC1-6, dialquilC1-6-amino-carbonil-alcoxiloC1-6, alquilC1-6-carboniloxi-alquiloC1-6, alquilC1-6-carboniloxi-alcoxiloC1-6, ciano-alquiloC1-6, ciano-alcoxiloC1-6, 2-oxo-oxazolidinil-alquiloC1-6, 2-oxo-oxazolidinil- alcoxiloC1-6, alcoxiC1-6-carbonil-alquiloC1-6, alcoxiC1-6-carbonil alcoxiloC1-6, alquilC1-6-sulfonilamino-alquiloC1-6, alquilC1-6-sulfonilamino-alcoxiloC1-6, (N-alquilC1-6)-alquilC1-6-sulfonilamino-alquiloC1-6, (N-alquilC1-6)-alquilC1-6- sulfonilamino-alcoxiloC2-7, alquilC1-6-amino-alquiloC1-6, alquilC1-6-amino-alcoxiloC2-7, dialquilC1-6-amino-alquilC1-6, dialquilC1-6-amino-alcoxiloC2-7, alquilC1-6-sulfonil-alquiloC1-6, alquilC1-6-sulfonil-alcoxiloC1-6, carboxi-alquioC1-6, carboxi- alcoxiloC1-6, carboxi-alcoxiC1-6-alquiloC1-6, alcoxiC1-6-alquilC1-6-carbonilo, acil-alcoxiC1-6-alquiloC1-6, (N-alquilC1-6)-alcoxiC1-6-carbonilamino, (N-hidroxi)-alquilC1-6-amino-carbonil-alquiloC1-6, (N-hidroxi)-alquilC1-6-aminocarbonil-alcoxiloC1- 6, (N-hidroxi)-aminocarbonil-alquiloC1-6, (N-hidroxi)-aminocarbonil-alcoxiloC1-6, alcoxiC1-6-aminocarbonil-alquiloC1-6, 6-alcoxi-aminocarbonil-alcoxiloC1-6, (N-alcoxiC1-6)-alquilC1-6-aminocarbonil-alquiloC1-6, (N-alcoxiC1-6)-alquilC1-6-aminocarbonil- alcoxiloC1-6, (N-acil)-alcoxiC1-6-alquilC1-6-amino, alcoxiC1-6-alquilC1-6-carbamoilo, (N-alquilC1-6)-alcoxiC1-6-alquilC1-6-carbamoilo, alcoxiC1-6-alquilC1-6-carbonilo, alcoxiC1-6-alquilC1-6-carbonil-amino, (N-alquilC1-6)-alcoxiC1-6-alquilC1-6- carbonilamino, 1-alcoxiC1-6-alquilC1-6-imidazol-2-ilo, 1-alcoxiC1-6-alquilC1-6-tetrazol-5-ilo, 5-alcoxiC1-6-alquilC1-6-tetrazol-1-ilo, 2-alcoxiC1-6-alquilC1-6-4-oxoimidazol-1-ilo, carbamoil-alquiloC1-6, carbamoil-alcoxiloC1-6, alquilC1-6-carbamoilo, dialquilC1-6-carbamoilo, alquilC1-6-sulfonilo, alquilC1-6-amidinilo, acetamidinil-alquiloC1-6, O-metil-oximil-alquil1C1-6, O,N-dimetilhidroxilamino-alquiloC1-6, cicloalquilC3-6-alcanoiloC1-6, aril-alcanoiloC1-6 o heterociclil-alcanoiloC1-6, y también piridilo, piridiloxilo, piridiltio, piridilamino, piridil-alquiloC1-6, piridil-alcoxiloC1-6, pirimidilo, pirimidiniloxilo, pirimidiniltio, pirimidinilamilo, pirimidinil-alquiloC1-6, pirimidinil-alcoxiloC1-6, tienilo, tienil-alquiloC1-6, tienil-alcoxiloC1-6, furilo, furil-alquiloC1-6 o furil-alcoxiloC1-6 sustituidos opcionalmente con halogeno, alquilo C1-6, alcoxilo C1-6 o dihidroxi-alquilC1-6-aminocarbonilo, piperidinoalquilo, piperidinoalcoxilo, piperidinoalcoxialquilo, morfolinoalquilo, morfolinoalcoxilo, morfolinoalcoxialquilo, piperazinoalquilo, piperazino-alcoxilo, piperazinoalcoxi-alquilo, [1,2,4]triazol-1-il-alquilo, [1,2,4]triazol-1-il-alcoxilo, [1,2,4]triazol-4-il-alquilo, [1,2,4]triazol-4-il-alcoxilo, [1,2,4]oxadiazol-5-il-alquilo, [1,2,4]oxadiazol-5-il-alcoxilo, 3-metil[1,2,4]oxadiazol-5-il-alquilo, 3-metil[1,2,4]oxadiazol-5-il-alcoxilo, 5-metil[1,2,4]-oxadiazol-3-il-alquilo, 5-metil[1,2,4]oxadiazol-3-il-alcoxilo, tetrazol-1-il-alquilo, tetrazol- 1-il-alcoxilo, tetrazol-2-il-alquilo, tetrazol-2-il-alcoxilo, tetrazol-5-il-alquilo, tetrazol-5-il-alcoxilo, 5-metil-tetrazol-1-il-alcoxilo, 5-metil-tetrazol-1-il-alcoxilo, tiazol-4-il-alquilo, tiazol-4-il-alcoxilo, oxazol-4-il-alquilo, oxazol-4-il- alcoxilo, 2-oxo-pirrolidinilo-alquilo, 2-oxopirrolidinilo-alcoxilo, imidazol-alquilo, imidazol-alcoxilo, 2-metilimidazol-2-il-alquilo, 2-metilimidazolil-alcoxilo o N-metilpiperazino-alquilo, N-metilpiperazino-alcoxilo, N-metilpiperazino-alcoxi- alquilo, dioxolanilo, dioxanilo, ditiolanilo, ditianilo, pirrolidinilo, piperidinilo, piperazinilo, pirrolilo, 4-metil-piperazinilo, morfolinilo, tiomorfolinilo, 2-hidroximetilpirrolidinilo, 3-hidroxi-pirrolidin-ilo, 3,4-dihidroxipirrolidinilo, 3- acetamidometilpirrolidinilo, 3-alcoxiC1-6-alquilC1-6-pirrolidinilo, 4-hidroxi-piperidinilo, 4-oxopiperidinilo, 3,5-dimetilmorfolinilo, 4,4-dioxo-tiomorfolinilo, 4-oxo-tiomorfonilo, 2,6-dimetilmorfolinilo, 2-oxoimidazolidinilo, 2-oxooxazolidinilo, 2- oxo-pirrolidinilo, 2-oxo[1,3]oxazinilo, 2-oxotetrahidropirimidinilo, y el radical -O-CH2CH(OH)CH2NRx en donde NRx, es un radical mono- o di-alquilC1-6-amino, piperidino, morfolino, piperazino o N-metilpiperazino; donde, en el caso de que R1 sea naftilo o ciclohexenofenilo, al menos el sistema anular no unido a X está sustituido como se específica; o C) R1 es pirazinilo, triazolilo, imidazolilo, benzotiazolilo, piranilo, tetrahidropiranilo, azetidinilo, morfolinilo, quinazolinilo, quinoxalinilo, isoquinolilo, benzo[b]tienilo, isobenzofuranilo, bencimidazolilo, 2-oxobencimidazolilo, oxazolilo, tiazolilo, pirrolilo, pirazolilo, triazinilo, dihidrobenzofuranilo, 2-oxodihidrobenzo[d][1,3]oxazinilo, 4-oxodihidroimidazolilo, 5-oxo- 4H-[1,2,4]triazinilo, 3-oxo-4H-benzo[1,4]tiazinilo, tetrahidroquinoxalinilo, 1,1,3-trioxohidro-2H-1lambda6-benzo[1,4]tiazinilo, 1-oxopiridilo, dihidro-3H-benzo[1,4]oxazinilo, 2-oxotetrahidrobenzo[e][1,4]diazepinilo, 2-oxodihidro- 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-dioxodihidro-2H-benzo-[1,4]tiazinilo, 2-oxo-1H- pirido[2,3-d][1,4]oxazinilo, dihidro-1H-pirido[2,3-b]-[1,4]oxazinilo, 1H-pirrol[2,3-b]piridilo, benzo[1,3]dioxolilo, benzooxazolilo, 2-oxo-benzooxazolilo, 2-oxo-1,3-dihidro-indol-ilo, 2,3-dihidroindolilo, indazolilo, benzofuranilo, dioxolanilo, dioxanilo, ditiolanilo, ditianilo, pirrolidinilo, piperidinilo, piperazinilo, 4-metil-piperazinilo, morfolinilo, tiomorfolinilo, 2-hidroximetilpirrolidinilo, 3-hidroxipirrolidinilo, 3,4-dihidroxi-pirrolidinilo, 4-hidroxipiperidinilo, 4- oxopiperidinilo, 3,5-dimetilmorfolinilo, 4,4-dioxo-tiomorfolin-ilo, 4-oxotiomorfolinilo, 2,6-dimetilmorfolinilo, tetrahidropiranilo, 2-oxo-imidazolidin-ilo, 2-oxo-oxazolidinilo, 2-oxo-piperidinilo, 2-oxo-pirrolidinilo, 2-oxo[1,3]-oxazinilo, 2- oxoazepanilo o 2-oxotetrahidropirimidinilo; R2 es alquilo C1-6 o cicloalquilo C3-8; R3 es independientemente entre sí H, alquilo C1-6 o alcanoilo C1-6; R4 es alquilo C1-6, cicloalquilo C3-8, alquenilo C2-6 o aril-alquiloC1-6 sin sustituir o sustituido; R5 es alquilo C1-6, hidroxialquilo C1-6, alcoxiC1-6-alquiloC1-6, alcanoiloxiC1-6-alquiloC1-6, aminoalquilo C1-6, alquilC1-6-amino-alquiloC1-6, dialquilC1-6-amino-alquiloC1-6, alcanoilC1-6-amido-alquiloC1-6, HO(O)C-alquiloC1-6, alquilC1-6- O-(O)C-alquiloC1-6, H2N-C(O)-alquiloC1-6, alquilC1-6-NH-C(O)-alquiloC1-6, (alquilC1-6)2-N-C(O)-alquiloC1-6, cicloalquilo C3-6 sin sustituir o sustituido o heterociclilo sin sustituir o sustituido; y su sal, en particular su sal farmacéuticamente util.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
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CH4692004 | 2004-03-19 |
Publications (1)
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AR048320A1 true AR048320A1 (es) | 2006-04-19 |
Family
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Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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ARP050101073A AR048320A1 (es) | 2004-03-19 | 2005-03-18 | Derivados de 5-amino-4-hidroxi-7-(1h-indolilmetil)-8-metilnonanamida |
Country Status (15)
Country | Link |
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US (1) | US7851634B2 (es) |
EP (4) | EP1699762A1 (es) |
JP (1) | JP2007529474A (es) |
CN (1) | CN1934083A (es) |
AR (1) | AR048320A1 (es) |
AT (1) | ATE421501T1 (es) |
BR (1) | BRPI0508961A (es) |
CA (1) | CA2560199A1 (es) |
DE (1) | DE602005012481D1 (es) |
ES (1) | ES2320030T3 (es) |
IL (1) | IL178100A0 (es) |
PL (1) | PL1717226T3 (es) |
PT (1) | PT1717226E (es) |
TW (1) | TW200536539A (es) |
WO (1) | WO2005090305A1 (es) |
Families Citing this family (18)
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TW200631929A (en) * | 2004-12-10 | 2006-09-16 | Speedel Experimenta Ag | ω -phenyloctanamides |
TW200633983A (en) * | 2004-12-10 | 2006-10-01 | Speedel Experimenta Ag | 5-Amino-4-hydroxy-2-isopropyl-7-[4-methoxy-3-(3-methoxypropoxy)benzyl]-8-methyl-nonanamides |
GB0505969D0 (en) | 2005-03-23 | 2005-04-27 | Novartis Ag | Organic compounds |
EP1764098A1 (en) * | 2005-09-17 | 2007-03-21 | Speedel Experimenta AG | Diaminoalcohols derivatives for the treatment of Alzheimer, malaria, HIV |
AR056197A1 (es) * | 2005-09-17 | 2007-09-26 | Speedel Experimenta Ag | Derivados de 7-metilimidazol[1,2-a]piridin-6-il-8-metil-nonamidas como inhibidores de la renina, composciones farmaceuticas que los contienen y su uso en la fabricacion de un medicamento para el tratamiento de la hipertension arterial |
GB0521083D0 (en) * | 2005-10-17 | 2005-11-23 | Novartis Ag | Organic compounds |
AR058885A1 (es) | 2005-12-30 | 2008-02-27 | Novartis Ag | Compuestos de piperidina 3,5-sustituidos |
AR059227A1 (es) * | 2006-01-30 | 2008-03-19 | Speedel Experimenta Ag | Proceso para la preparacion de compuestos organicos |
TW200831463A (en) * | 2006-09-12 | 2008-08-01 | Speedel Experimenta Ag | Nitrate esters of aminoalcohols |
EP1911762A1 (en) * | 2006-10-04 | 2008-04-16 | Speedel Experimenta AG | Amino alcohols and their use as renin inhibitors |
EP1921069A1 (de) * | 2006-11-08 | 2008-05-14 | Speedel Experimenta AG | Verfahren zur Herstellung von 2-Alkyl-3-heterocyclyl-prop-2-en-1-olen |
EP1939182A1 (de) * | 2006-12-22 | 2008-07-02 | Speedel Experimenta AG | Verfahren zur Herstellung von (R oder S)-2-Alkyl-3-heterocyclyl-1-propanolen |
AR065792A1 (es) * | 2007-03-21 | 2009-07-01 | Speedel Experimenta Ag | Proceso para preparar (r o s) -5- (1 -azido-3-(6-metoxi-5-(3-metoxi-propoxi) -piridin-3-ilmetil) -4-metil- pentil) -3-alquil-dihidro-furan-2-ona |
CN101687847B (zh) | 2007-06-25 | 2013-11-06 | 诺华股份有限公司 | 用作肾素抑制剂的n5-(2-乙氧基乙基)-n3-(2-吡啶基)-3,5-哌啶二甲酰胺衍生物 |
EP2163245A1 (en) | 2008-09-10 | 2010-03-17 | Novartis Ag | Renin inhibitors for the treatment of psoriasis |
AR077428A1 (es) * | 2009-07-29 | 2011-08-24 | Sanofi Aventis | (aza) indolizinacarboxamidas ciclicas su preparacion y su uso como agentes farmaceuticos |
WO2011051853A1 (en) | 2009-10-29 | 2011-05-05 | CarboDesign LLC | Manufacturing process for preparing enaniomerically pure 8- aryloctanoic acid derivatives such as aliskiren |
US8703976B2 (en) | 2011-10-02 | 2014-04-22 | Milan Soukup | Manufacturing process for 8-aryloctanoic acids such as Aliskiren |
Family Cites Families (8)
Publication number | Priority date | Publication date | Assignee | Title |
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US5659065A (en) | 1994-04-18 | 1997-08-19 | Novartis Corporation | Alpha-aminoalkanoic acids and reduction products |
MY119161A (en) | 1994-04-18 | 2005-04-30 | Novartis Ag | Delta-amino-gamma-hydroxy-omega-aryl-alkanoic acid amides with enzyme especially renin inhibiting activities |
US5606078A (en) | 1994-04-18 | 1997-02-25 | Ciba-Geigy Corporation | 3,5-Disubstituted tetrahydrofuran-2-ones |
EP0702004A2 (de) * | 1994-09-15 | 1996-03-20 | Ciba-Geigy Ag | 2,9-Diamino- und 2-amino-8-carbamoyl-4-hydroxy-alkansäureamid-derivative |
EP0716077A1 (de) * | 1994-12-08 | 1996-06-12 | Ciba-Geigy Ag | Aromatisch substituierte Omega-Aminoalkansäureamide und Alkansäurediamide und ihre Verwendung als Renininhibitoren |
WO2001098294A2 (en) * | 2000-06-21 | 2001-12-27 | Bristol-Myers Squibb Pharma Company | Vitronectin receptor antagonist pharmaceuticals for use in combination therapy |
US6897231B2 (en) * | 2000-07-31 | 2005-05-24 | Signal Pharmaceuticals, Inc. | Indazole derivatives as JNK inhibitors and compositions and methods related thereto |
AU2003238007A1 (en) * | 2002-06-11 | 2003-12-22 | Elan Pharmaceuticals, Inc. | Methods of treating alzheimer's disease using aryl alkanoic acid amides |
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2005
- 2005-03-17 EP EP05729684A patent/EP1699762A1/en not_active Withdrawn
- 2005-03-17 BR BRPI0508961-1A patent/BRPI0508961A/pt not_active IP Right Cessation
- 2005-03-17 PT PT06117363T patent/PT1717226E/pt unknown
- 2005-03-17 US US10/593,460 patent/US7851634B2/en not_active Expired - Fee Related
- 2005-03-17 ES ES06117363T patent/ES2320030T3/es active Active
- 2005-03-17 EP EP06117357A patent/EP1724259A1/en not_active Withdrawn
- 2005-03-17 EP EP06117361A patent/EP1712548A3/en not_active Withdrawn
- 2005-03-17 WO PCT/EP2005/051244 patent/WO2005090305A1/en not_active Application Discontinuation
- 2005-03-17 PL PL06117363T patent/PL1717226T3/pl unknown
- 2005-03-17 TW TW094108176A patent/TW200536539A/zh unknown
- 2005-03-17 EP EP06117363A patent/EP1717226B1/en not_active Not-in-force
- 2005-03-17 DE DE602005012481T patent/DE602005012481D1/de active Active
- 2005-03-17 AT AT06117363T patent/ATE421501T1/de active
- 2005-03-17 CN CNA2005800087273A patent/CN1934083A/zh active Pending
- 2005-03-17 CA CA002560199A patent/CA2560199A1/en not_active Abandoned
- 2005-03-17 JP JP2007503352A patent/JP2007529474A/ja active Pending
- 2005-03-18 AR ARP050101073A patent/AR048320A1/es unknown
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- 2006-09-14 IL IL178100A patent/IL178100A0/en unknown
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US7851634B2 (en) | 2010-12-14 |
PL1717226T3 (pl) | 2009-07-31 |
BRPI0508961A (pt) | 2007-08-14 |
TW200536539A (en) | 2005-11-16 |
JP2007529474A (ja) | 2007-10-25 |
EP1699762A1 (en) | 2006-09-13 |
EP1717226A1 (en) | 2006-11-02 |
CN1934083A (zh) | 2007-03-21 |
ES2320030T3 (es) | 2009-05-18 |
WO2005090305A1 (en) | 2005-09-29 |
IL178100A0 (en) | 2006-12-31 |
DE602005012481D1 (de) | 2009-03-12 |
EP1717226B1 (en) | 2009-01-21 |
EP1712548A3 (en) | 2006-11-02 |
EP1712548A2 (en) | 2006-10-18 |
PT1717226E (pt) | 2009-04-03 |
EP1724259A1 (en) | 2006-11-22 |
US20080280895A1 (en) | 2008-11-13 |
ATE421501T1 (de) | 2009-02-15 |
CA2560199A1 (en) | 2005-09-29 |
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