AR040138A1 - Combinacion de compuestos, conjunto de partes (kit), metodo para preparar un conjunto de partes (kit) y uso de dicha combinacion de compuestos en la fabricacion de un medicamento - Google Patents
Combinacion de compuestos, conjunto de partes (kit), metodo para preparar un conjunto de partes (kit) y uso de dicha combinacion de compuestos en la fabricacion de un medicamentoInfo
- Publication number
- AR040138A1 AR040138A1 ARP030101881A ARP030101881A AR040138A1 AR 040138 A1 AR040138 A1 AR 040138A1 AR P030101881 A ARP030101881 A AR P030101881A AR P030101881 A ARP030101881 A AR P030101881A AR 040138 A1 AR040138 A1 AR 040138A1
- Authority
- AR
- Argentina
- Prior art keywords
- oxa
- diazabicyclo
- alkyl
- aryl
- benzonitrile
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title abstract 7
- 238000004519 manufacturing process Methods 0.000 title 1
- 229940126601 medicinal product Drugs 0.000 title 1
- 238000000034 method Methods 0.000 title 1
- 125000003118 aryl group Chemical group 0.000 abstract 19
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 18
- 125000005843 halogen group Chemical group 0.000 abstract 14
- 125000001424 substituent group Chemical group 0.000 abstract 13
- -1 3,4-dimethoxyphenoxy Chemical group 0.000 abstract 11
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 10
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 10
- 125000002947 alkylene 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
- 125000004400 (C1-C12) alkyl group Chemical group 0.000 abstract 3
- 125000000217 alkyl group Chemical group 0.000 abstract 3
- 125000004430 oxygen atom Chemical group O* 0.000 abstract 3
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 abstract 2
- 125000003161 (C1-C6) alkylene group Chemical group 0.000 abstract 2
- 125000004104 aryloxy group Chemical group 0.000 abstract 2
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 abstract 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 2
- 125000001153 fluoro group Chemical group F* 0.000 abstract 2
- 229910052760 oxygen Inorganic materials 0.000 abstract 2
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 abstract 2
- OQHPAEHSQMKXSG-UHFFFAOYSA-N (3-benzoyl-9-oxa-3,7-diazabicyclo[3.3.1]nonan-7-yl)-phenylmethanone Chemical compound C=1C=CC=CC=1C(=O)N(CC(C1)O2)CC2CN1C(=O)C1=CC=CC=C1 OQHPAEHSQMKXSG-UHFFFAOYSA-N 0.000 abstract 1
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 1
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract 1
- YJYJPLYZJGTMIH-KPQWGBOZSA-N 4-[(2s)-2-amino-3-[7-(2-pyrrol-1-ylethyl)-9-oxa-3,7-diazabicyclo[3.3.1]nonan-3-yl]propoxy]benzonitrile Chemical compound C([C@@H](N)CN1CC2CN(CCN3C=CC=C3)CC(O2)C1)OC1=CC=C(C#N)C=C1 YJYJPLYZJGTMIH-KPQWGBOZSA-N 0.000 abstract 1
- QUXJOPAIAIISAV-UHFFFAOYSA-N 4-[1-(3,4-dimethoxyphenoxy)-4-[3-(3,3-dimethyl-2-oxobutyl)-9-oxa-3,7-diazabicyclo[3.3.1]nonan-7-yl]butyl]benzonitrile Chemical compound C1=C(OC)C(OC)=CC=C1OC(C=1C=CC(=CC=1)C#N)CCCN1CC(O2)CN(CC(=O)C(C)(C)C)CC2C1 QUXJOPAIAIISAV-UHFFFAOYSA-N 0.000 abstract 1
- BYJIWSCHQPNARL-UHFFFAOYSA-N 4-[1-(3,4-dimethoxyphenoxy)-4-[3-[2-(3,4-dimethoxyphenyl)ethyl]-9-oxa-3,7-diazabicyclo[3.3.1]nonan-7-yl]butyl]benzonitrile Chemical compound C1=C(OC)C(OC)=CC=C1CCN1CC(O2)CN(CCCC(OC=3C=C(OC)C(OC)=CC=3)C=3C=CC(=CC=3)C#N)CC2C1 BYJIWSCHQPNARL-UHFFFAOYSA-N 0.000 abstract 1
- SYJFQACWAVOYBU-UHFFFAOYSA-N 4-[2-(3-butylsulfonyl-9-oxa-3,7-diazabicyclo[3.3.1]nonan-7-yl)ethoxy]benzonitrile Chemical compound C1C(O2)CN(S(=O)(=O)CCCC)CC2CN1CCOC1=CC=C(C#N)C=C1 SYJFQACWAVOYBU-UHFFFAOYSA-N 0.000 abstract 1
- RYYDXQOTNIVFHE-UHFFFAOYSA-N 4-[2-[3-(3,3-dimethyl-2-oxobutyl)-9-oxa-3,7-diazabicyclo[3.3.1]nonan-7-yl]ethoxy]benzonitrile Chemical compound C1C(O2)CN(CC(=O)C(C)(C)C)CC2CN1CCOC1=CC=C(C#N)C=C1 RYYDXQOTNIVFHE-UHFFFAOYSA-N 0.000 abstract 1
- HHHBDMKCXKKOIA-UHFFFAOYSA-N 4-[2-[3-(3,3-dimethyl-2-oxobutyl)-9-oxa-3,7-diazabicyclo[3.3.1]nonan-7-yl]ethyl]benzonitrile Chemical compound C1C(O2)CN(CC(=O)C(C)(C)C)CC2CN1CCC1=CC=C(C#N)C=C1 HHHBDMKCXKKOIA-UHFFFAOYSA-N 0.000 abstract 1
- QDXSQVTXOFFIFI-UHFFFAOYSA-N 4-[2-[3-[2-(4-methoxyphenyl)-2-oxoethyl]-9-oxa-3,7-diazabicyclo[3.3.1]nonan-7-yl]ethoxy]benzonitrile Chemical compound C1=CC(OC)=CC=C1C(=O)CN1CC(O2)CN(CCOC=3C=CC(=CC=3)C#N)CC2C1 QDXSQVTXOFFIFI-UHFFFAOYSA-N 0.000 abstract 1
- VDMBYWYDYJFUAG-UHFFFAOYSA-N 4-[2-[7-(4-pyridin-4-ylbutyl)-9-oxa-3,7-diazabicyclo[3.3.1]nonan-3-yl]ethoxy]benzonitrile Chemical compound C1=CC(C#N)=CC=C1OCCN1CC(O2)CN(CCCCC=3C=CN=CC=3)CC2C1 VDMBYWYDYJFUAG-UHFFFAOYSA-N 0.000 abstract 1
- PFOCXRBQPDHSAT-UHFFFAOYSA-N 4-[2-[7-[2-(3,4-dimethoxyphenyl)ethyl]-9-oxa-3,7-diazabicyclo[3.3.1]nonan-3-yl]ethoxy]benzonitrile Chemical compound C1=C(OC)C(OC)=CC=C1CCN1CC(O2)CN(CCOC=3C=CC(=CC=3)C#N)CC2C1 PFOCXRBQPDHSAT-UHFFFAOYSA-N 0.000 abstract 1
- PRAXUAILYHAJER-UHFFFAOYSA-N 4-[3-(3-butylsulfonyl-9-oxa-3,7-diazabicyclo[3.3.1]nonan-7-yl)-2-hydroxypropoxy]benzonitrile Chemical compound C1C(O2)CN(S(=O)(=O)CCCC)CC2CN1CC(O)COC1=CC=C(C#N)C=C1 PRAXUAILYHAJER-UHFFFAOYSA-N 0.000 abstract 1
- JAHWBGQNAOVQRH-UHFFFAOYSA-N 4-[3-(3-butylsulfonyl-9-oxa-3,7-diazabicyclo[3.3.1]nonan-7-yl)propylamino]benzonitrile Chemical compound C1C(O2)CN(S(=O)(=O)CCCC)CC2CN1CCCNC1=CC=C(C#N)C=C1 JAHWBGQNAOVQRH-UHFFFAOYSA-N 0.000 abstract 1
- WDXMNFWBNDQQHC-UHFFFAOYSA-N 4-[3-[3-(3,3-dimethyl-2-oxobutyl)-9-oxa-3,7-diazabicyclo[3.3.1]nonan-7-yl]-2-hydroxypropoxy]benzonitrile Chemical compound C1C(O2)CN(CC(=O)C(C)(C)C)CC2CN1CC(O)COC1=CC=C(C#N)C=C1 WDXMNFWBNDQQHC-UHFFFAOYSA-N 0.000 abstract 1
- KZOCHEDMAHPYCK-UHFFFAOYSA-N 4-[3-[3-(3,3-dimethyl-2-oxobutyl)-9-oxa-3,7-diazabicyclo[3.3.1]nonan-7-yl]propylamino]benzonitrile Chemical compound C1C(O2)CN(CC(=O)C(C)(C)C)CC2CN1CCCNC1=CC=C(C#N)C=C1 KZOCHEDMAHPYCK-UHFFFAOYSA-N 0.000 abstract 1
- WVYRPQWKUKIKTK-UHFFFAOYSA-N 4-[3-[3-[2-(3,4-dimethoxyphenyl)ethyl]-9-oxa-3,7-diazabicyclo[3.3.1]nonan-7-yl]propylamino]benzonitrile Chemical compound C1=C(OC)C(OC)=CC=C1CCN1CC(O2)CN(CCCNC=3C=CC(=CC=3)C#N)CC2C1 WVYRPQWKUKIKTK-UHFFFAOYSA-N 0.000 abstract 1
- CGNLWYPSUVHSSD-UHFFFAOYSA-N 4-[3-[7-[(4-fluorophenyl)methyl]-9-oxa-3,7-diazabicyclo[3.3.1]nonan-3-yl]-2-hydroxypropoxy]benzonitrile Chemical compound C1C(O2)CN(CC=3C=CC(F)=CC=3)CC2CN1CC(O)COC1=CC=C(C#N)C=C1 CGNLWYPSUVHSSD-UHFFFAOYSA-N 0.000 abstract 1
- OVGLTWMZTWWVDG-UHFFFAOYSA-N 4-[3-[7-[2-(3,4-dimethoxyphenyl)ethyl]-9-oxa-3,7-diazabicyclo[3.3.1]nonan-3-yl]-2-hydroxypropoxy]benzonitrile Chemical compound C1=C(OC)C(OC)=CC=C1CCN1CC(O2)CN(CC(O)COC=3C=CC(=CC=3)C#N)CC2C1 OVGLTWMZTWWVDG-UHFFFAOYSA-N 0.000 abstract 1
- NNIHXAQWSNOUEP-UHFFFAOYSA-N 4-[4-(3-butylsulfonyl-9-oxa-3,7-diazabicyclo[3.3.1]nonan-7-yl)-1-(3,4-dimethoxyphenoxy)butyl]benzonitrile Chemical compound C1C(O2)CN(S(=O)(=O)CCCC)CC2CN1CCCC(C=1C=CC(=CC=1)C#N)OC1=CC=C(OC)C(OC)=C1 NNIHXAQWSNOUEP-UHFFFAOYSA-N 0.000 abstract 1
- 125000004801 4-cyanophenyl group Chemical group [H]C1=C([H])C(C#N)=C([H])C([H])=C1* 0.000 abstract 1
- 101000712605 Theromyzon tessulatum Theromin Proteins 0.000 abstract 1
- 229940122388 Thrombin inhibitor Drugs 0.000 abstract 1
- 239000008186 active pharmaceutical agent Substances 0.000 abstract 1
- 125000004186 cyclopropylmethyl group Chemical group [H]C([H])(*)C1([H])C([H])([H])C1([H])[H] 0.000 abstract 1
- 125000004428 fluoroalkoxy group Chemical group 0.000 abstract 1
- 239000012634 fragment Substances 0.000 abstract 1
- 125000005842 heteroatom Chemical group 0.000 abstract 1
- 125000000623 heterocyclic group Chemical group 0.000 abstract 1
- 125000004043 oxo group Chemical group O=* 0.000 abstract 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 1
- 229910052717 sulfur Inorganic materials 0.000 abstract 1
- JRHUUZPSMQIWBQ-PELRDEGISA-N tert-butyl n-[2-[3-[(2s)-3-(4-cyanophenoxy)-2-hydroxypropyl]-9-oxa-3,7-diazabicyclo[3.3.1]nonan-7-yl]ethyl]carbamate Chemical compound C([C@@H](O)CN1CC2CN(CC(C1)O2)CCNC(=O)OC(C)(C)C)OC1=CC=C(C#N)C=C1 JRHUUZPSMQIWBQ-PELRDEGISA-N 0.000 abstract 1
- AODMXGLAXUKWMG-UHFFFAOYSA-N tert-butyl n-[2-[7-(4-pyridin-4-ylbutyl)-9-oxa-3,7-diazabicyclo[3.3.1]nonan-3-yl]ethyl]carbamate Chemical compound C1C(O2)CN(CCNC(=O)OC(C)(C)C)CC2CN1CCCCC1=CC=NC=C1 AODMXGLAXUKWMG-UHFFFAOYSA-N 0.000 abstract 1
- LAMDSCRMEIOKJI-UHFFFAOYSA-N tert-butyl n-[2-[7-[3-(4-cyanoanilino)propyl]-9-oxa-3,7-diazabicyclo[3.3.1]nonan-3-yl]ethyl]carbamate Chemical compound C1C(O2)CN(CCNC(=O)OC(C)(C)C)CC2CN1CCCNC1=CC=C(C#N)C=C1 LAMDSCRMEIOKJI-UHFFFAOYSA-N 0.000 abstract 1
- ZEEVEFOISWRYMK-UHFFFAOYSA-N tert-butyl n-[2-[7-[4-(4-cyanophenyl)butyl]-9-oxa-3,7-diazabicyclo[3.3.1]nonan-3-yl]ethyl]carbamate Chemical compound C1C(O2)CN(CCNC(=O)OC(C)(C)C)CC2CN1CCCCC1=CC=C(C#N)C=C1 ZEEVEFOISWRYMK-UHFFFAOYSA-N 0.000 abstract 1
- 239000003868 thrombin inhibitor Substances 0.000 abstract 1
Classifications
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/397—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having four-membered rings, e.g. azetidine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/401—Proline; Derivatives thereof, e.g. captopril
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/5386—1,4-Oxazines, e.g. morpholine spiro-condensed or forming part of bridged ring systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
-
- 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
- A61P9/06—Antiarrhythmics
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D205/00—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom
- C07D205/02—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings
- C07D205/04—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
-
- 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
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Epidemiology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Diabetes (AREA)
- Hematology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Pyrrole Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Plural Heterocyclic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
Una combinación de compuestos que comprende (a) compuestos inhibidores de trombina de la fórmula (1) donde Ra representa -OH o -CH2OH; R1 representa por lo menos un sustituyente halo optativo; R2 representa uno o dos C1-3 sustituyentes alcoxi, tal que las partes alquilo de dichos sustituyentes están ellos mismos sustituidos con uno o más sustituyentes fluoro (es decir que R2 representa uno o dos grupos fluoroalcoxi (C1-3)); Y representa -CH2- o -(CH2)2-; y R3 representa un fragmento estructural de la fórmula (2) o de la fórmula (3) donde R4 representa H o uno o más sustituyentes fluoro; y uno o dos de X1, X2, X3 y X4 representan -N- y los otros representan -CH-, o un derivado aceptable para uso farmacéutico del mismo y (b) (1) Un compuesto de la fórmula (4) donde R1 representa C1-12 alquilo,(donde dicho grupo alquilo está sustituido y/o terminado optativamente por uno o más grupos seleccionados entre halo, ciano, nitro, arilo, Het1, -C(O)R5a, -OR5b-, -N(R6)R5c, -C(O)XR7, -C(O)N(R8)R5d, y -S(O)2R9, o R1 representa -C(O)XR7, -C(O)N(R8)R5d o -S(O)2R9; R5a a R5d representan independientemente en cada caso H, C1-6alquilo (donde el último grupo está sustituido y/o terminado optativamente por uno o más sustituyentes seleccionados entre -OH, halo, ciano, nitro, arilo y Het2), arilo o Het3, o R5d, junto con R8, representa C3-6 alquileno (donde dicho grupo alquileno está interrumpido optativamente por un átomo de O y/o está sustituido optativamente por uno o más C1-3 grupos alquilo); R6 representa H, C1-6 alquilo (sustituido y/o terminado optativamente por uno o más sustituyentes seleccionados entre -OH, halo, ciano, nitro y arilo), arilo, -C(O)R10a, -C(O)OR10b o -C(O)N(H)R10c, R10a, R10b y R10c representan independientemente C1-6 alquilo (sustituido y/o terminado optativamente por uno o más sustituyentes seleccionados entre -OH, halo, ciano, nitro y arilo), arilo, o R10a representa H; R7 representa C1-12 alquilo (sustituido y/o terminado optativamente por uno más sustituyentes seleccionados entre -OH, halo, ciano, nitro, arilo, C1-6 alcoxi y Het4); R8 representa H, C1-12 alquilo, C1-6 alcoxi (donde dichos dos últimos grupos están sustituidos y/o terminados optativamente por uno o más sustituyentes seleccionados entre -OH, halo, ciano, nitro, C1-4 alquilo y C1-4 alcoxi), -D-arilo, -D-ariloxi, -D-Het5, -D-N(H)C(O)R11a, -D-S(O)2R12a, -D-C(O)R11b, -D-C(O)OR12b, -D-C(O)N(R11c)R11d, o R8, junto con R5d, representa C3-6 alquileno ( donde dicho grupo alquileno está interrumpido optativamente por un átomo de O y/o está sustituido optativamente por uno o más C1-3 grupos alquilo); R11a a R11d representan independientemente H, C1-6 alquilo (sustituido y/o terminado optativamente por uno o más sustituyentes seleccionados entre -OH, halo, ciano, nitro y arilo), arilo, o R11c y R11d juntos representan C3-6 alquileno; R9, R12a y R12b representan independientemente C1-6 alquilo (sustituido y/o terminado optativamente por uno o más sustituyentes seleccionados entre -OH, halo, ciano, nitro y arilo), o arilo; D representa un enlace directo o C1-6 alquileno; X representa O o S; R2 representa H, halo, C1-6 alquilo, -OR13, -E-N(R14)R15 o, junto con R3, representa =O; R3 representa H, C1-6 alquilo o, junto con R2, representa =O; R13 representa H, C1-6 alquilo, -E-arilo, -E-Het6, -C(O)R16a, -C(O)OR16b o -C(O)N(R17a)R17b; R14 representa H, C1-6 alquilo, -E-arilo, -E-Het8, -C(O)R16a, -C(O)OR16b, -S(O)2R16c, -[C(O)]pN(R17a)R17b o -C(NH)NH2; R15 representa H, C1-6 alquilo, -E-arilo o -C(O)R13d; R16a a R16d representan independientemente, en cada caso cuando se utilizan en la presenta C1-6 alquilo (sustituido y/o terminado optativamente por uno o más sustituyentes seleccionados entre halo, arilo y Het7), arilo, Het8 o R16a y R16d representan independientemente H, R17a y R17b representan independientemente, en cada caso cuando se utilizan en la presente, H o C1-6 alquilo (sustituido y/o terminado optativamente por uno o más sustituyentes seleccionados entre halo, arilo y Het9), arilo, Het10, o juntos representan C3-6alquileno, optativamente interrumpido por un átomo de O; E representa, en cada caso cuando se utiliza en la presente, un enlace directo o C1-4 alquileno; p representa 1 o 2; Het1 a Het10 representan independientemente grupos heterocíclicos de cinco a doce miembros que contienen uno o más heteroátomos seleccionados entre O, N y/o S, donde dichos grupos están sustituidos optativamente por uno o más sustituyentes seleccionados entre -OH, oxo, halo, ciano, nitro, C1-6 alquilo, C1-6 alcoxi, arilo, ariloxi, -N(R18a)R18b, -C(O)R18c, -C(O)OR18d, -C(O)N(R18e)R18f, -N(R18g)C(O)R18h y -N(R18i)S(O)2R18j; R18a a R18j representan independientemente C1-6 alquilo, arilo o R18a a R18j representan independientemente H; A representa un enlace directo, -J-, -J-N(R19)- o -J-O- (donde en dichos dos últimos grupos, N(R19)- u O está unido al átomo de C ligado a R2 y R3); B representa -Z-, -Z-N(R20)-, -N(R20)-Z-, -Z-S(O)n-, -Z-O-( donde en dichos dos últimos grupos, Z está unido al átomo de C ligado a R2 y R3), -N(R20)C(O)O-Z-, (donde en este último grupo, -N(R20) está unido al átomo de C ligado a R2 y R3) o -C(O)N(R20)- (donde en este último gripo, -C(O) está unido al átomo de C ligado a R2 y R3); J representa C1-6 alquileno sustituido optativamente por uno o más sustituyentes seleccionados entre -OH, halo, y amino; Z representa un enlace directo o C1-4 alquileno; n representa 0, 1 o 2; R19 y R20 representan independientemente H o C1-6 alquilo; G representa CH o N; R4 representa uno o más sustituyentes opcionales seleccionados entre -OH, ciano, halo, nitro, C1-6 alquilo ( terminado optativamente por -N(H)C(O)OR21a),C1-6 alcoxi, -N(R22a)R22b, -C(O)R22c, -C(O)OR22d, -C(O)N(R22e)R22f, N(R22g)C(O)R22h, -N(R22i)C(O)N(R22j)R22k, -N(R22m)S(O)2R21b, -S(O)2R21c, y/o -OS(O)2R21d, R21a a R21d representan independientemente C1-6 alquilo; R22a y R22b representan independientemente H, C1-6 alquilo o juntos representan C3-6 alquileno, dando como resultado un anillo de cuatro a siete miembros que contiene N; R22c a R22m representan independientemente H o C1-6 alquilo; y R41 a R46 representan independientemente H o C1-3 alquilo; donde cada grupo arilo y ariloxi, salvo que se indique lo contrario, está sustituido opcionalmente; con la condición de que (a) el compuesto no sea 3,7-dibenzoil-9-oxa-3,7-diazabiciclo[3.3.1]nonano; (b) cuando A representa -J-N(R19)- o -J-O-, entonces (i) J no representa C1alquileno; y (ii) B no representa -N(R20)-, -N(R20)-Z- (donde en este último grupo N(R20) está unido al átomo de C ligado a R2 y R3), -S(O)n-, -O- o -N(R20)C(O)O-Z- cuando R2 y R3 juntos no representan =O; y (c) cuando R2 representa -OR13 o -N(R14)(R15), entonces (i) A no representa -J-N(R19)- o -J-O-; y (ii) B no representa -N(R20)-, -N(R20)-Z- (donde en este último grupo N(R20) está unido al átomo de C ligado a R2 y R3), -S(O)n-, -O- o -N(R20)C(O)O-Z-; o un derivado aceptable para uso farmacéutico del mismo, o (2) Un compuesto que es: 4-{2-[7-(3,3-dimetil-2-oxobutil)-9-oxa-3,7-diazabiciclo[3.3.1]non-3-il]etil}benzonitrilo; 7-[4-(-cianofenil)-4-(3,4-dimetoxifenoxi)butil]-N-etil-9-oxa-3,7-diazabiciclo[3.3.1]nonano-3-carboxamida; 4-({3-[7-(3,3-dimetil-2-oxobutil)-9-oxa-3,7-diazabiciclo[3.3.1]non-3-il]propil}amino)benzonitrilo; 4-{3-[7-(4-fluorobenzil)-9-oxa-3,7-diazabiciclo[3.3.1]non-3-il]-2-hidroxipropoxi}benzonitrilo; 4-(2-{7-[2-(4-metoxifenil)-2-oxoetil]-9-oxa-3,7-diazabiciclo[3.3.1]non-3-il}etoxi)benzonitrilo; 4-[((2S)-2-amino-3-{7-[2-(1H-pirrol-1-il)etil]-9-oxa-3,7-diazabiciclo-[3.3.1]non-3-il}propil)oxi]benzonitrilo; tert-butilo 2-{7-[3-(4-cianoanilino)propil]-9-oxa-3,7-diazabiciclo[3.3.1]-non-3-il}etilcarbamato; tert-butilo 2-{7-[4-(4-cianofenil)butil]-9-oxa-3,7-diazabiciclo[3.3.1]-non-3-il}etilcarbamato; tert-butilo 2-{7-[(2S)-3-(4-cianofenoxi)-2-hidroxipropil]-9-oxa-3,7-diazabiciclo[3.3.1]non-3-il}etilcarbamato; 4-(2-{7-[4-(4-piridinil)butil]-9-oxa-3,7-diazabiciclo[3.3.1]non-3-il}-etoxi)benzonitrilo; tert-butilo 2-{7-[4-(4-piridinil)butil]-9-oxa-3,7-diazabiciclo[3.3.1]non-3-il}etilcarbamato; 4-{3-[7-(3,3-dimetil-2-oxobutil)-9-oxa-3,7-diazabiciclo[3.3.1]non-3-il]-2-hidroxipropoxi}benzonitrilo; 4-{3-[7-(3,4-dimetoxifenetil)-9-oxa-3,7-diazabiciclo[3.3.1]non-3-il]-2-hidroxipropoxi}benzonitrilo; 4-{2-[7-(3,3-dimetil-2-oxobutil)-9-oxa-3,7-diazabiciclo[3.3.1]non-3-il]-etoxi}benzonitrilo; 4-({3-[7-(butilsulfonil)-9-oxa-3,7-diazabiciclo[3.3.1]non-3-il]propil}-amino)benzonitrilo; 4-({3-[7-(3,4-dimetoxifenetil)-9-oxa-3,7-diazabiciclo[3.3.1]non-3-il]propil}amino)benzonitrilo; 4-[4-[7-(butilsulfonil)-9-oxa-3,7-diazabiciclo[3.3.1]non-3-il]-1-(3,4-dimetoxifenoxi)butil]benzonitrilo; 4-{1-(3,4-dimetoxifenoxi)-4-[7-(3,3-dimetil-2-oxobutil)-9-oxa-3,7-diazabiciclo[3.3.1]non-3-il]butil}benzonitrilo; 4-[4-[7-(3,4-dimetoxifenetil)-9-oxa-3,7-diazabiciclo[3.3.1]non-3-il]-1-(3,4-dimetoxifenoxi)butil]benzonitrilo; 7-[3-(4-cianofenoxi)-2-hidroxipropil]-9-oxa-3,7-diazabiciclo[3.3.1]nonano-3-carboxilato de 2-(4-acetil-1-piperazinil)etilo; 7-[3-(4-cianofenoxi)-2-hidroxipropil]-N-etil-9-oxa-3,7-diazabiciclo-[3.3.1]nonano-3-carboxamida; 4-{3-[7-(butilsulfonil)-9-oxa-3,7-diazabiciclo[3.3.1]non-3-il]-2-hidroxipropoxi}benzonitrilo; 7-[2-(4-cianofenoxi)etil]-9-oxa-3,7-diazabiciclo[3.3.1]nonano-3-carboxilato de 2-(4-acetil-1-piperazinil)etilo; 7-[2-(4-cianofenoxi)etil]-N-etil-9-oxa-3,7-diazabiciclo[3.3.1]-nonano-3-carboxamida; 4-{2-[7-(butilsulfonil)-9-oxa-3,7-diazabiciclo[3.3.1]non-3-il]etoxi}-benzonitrilo; 4-{2-[7-(3,4-dimetoxifenetil)-9-oxa-3,7-diazabiciclo[3.3.1]non-3-il]etoxi}benzonitrilo; 7-[3-(4-cianoanilino)propil]-9-oxa-3,7-diazabiciclo[3.3.1]nonano-3-carboxilato de 2-(4-acetil-1-piperazinil)etilo; 7-[3-(4-cianoanilino)propil]-N-etil-9-oxa-3,7-diazabiciclo[3.3.1]-nonano-3-carboxamida; 7-[4-(4-cianofenil)-4-(3,4-dimetoxi-fenoxi)butil]-9-oxa-3,7-diazabiciclo[3.3.1]nonano-3-carboxilato de 2-(4-acetil-1-piperazinil)etilo; 4-{3-[7-(ciclopropilmetil)-9-oxa-3,7-diazabiciclo[3.3.1]non-3-il]-2-hidroxipropoxi}benz
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SE0201662A SE0201662D0 (sv) | 2002-05-31 | 2002-05-31 | Pharmaceutical combination |
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| AR040138A1 true AR040138A1 (es) | 2005-03-16 |
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| ARP030101881A AR040138A1 (es) | 2002-05-31 | 2003-05-28 | Combinacion de compuestos, conjunto de partes (kit), metodo para preparar un conjunto de partes (kit) y uso de dicha combinacion de compuestos en la fabricacion de un medicamento |
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| Country | Link |
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| US (1) | US20060052314A1 (es) |
| EP (1) | EP1513807A1 (es) |
| JP (1) | JP2005532345A (es) |
| CN (1) | CN1656066A (es) |
| AR (1) | AR040138A1 (es) |
| AU (1) | AU2003232711A1 (es) |
| BR (1) | BR0311138A (es) |
| CA (1) | CA2486110A1 (es) |
| CO (1) | CO5631429A2 (es) |
| IL (1) | IL165169A0 (es) |
| IS (1) | IS7581A (es) |
| MX (1) | MXPA04011910A (es) |
| NO (1) | NO20044673L (es) |
| PL (1) | PL373409A1 (es) |
| RU (1) | RU2004131868A (es) |
| SE (1) | SE0201662D0 (es) |
| TW (1) | TW200307686A (es) |
| WO (1) | WO2003101956A1 (es) |
| ZA (1) | ZA200408787B (es) |
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| SE0401539D0 (sv) | 2004-06-15 | 2004-06-15 | Astrazeneca Ab | New compounds |
| EP1893619A1 (en) | 2005-06-13 | 2008-03-05 | AstraZeneca AB | New oxabispidine compounds for the treatment of cardiac arrhytmias |
| WO2006137772A1 (en) * | 2005-06-20 | 2006-12-28 | Astrazeneca Ab | New physical form of n,n´- disubstituted oxabispidines |
| JP5114880B2 (ja) * | 2006-07-06 | 2013-01-09 | ダイキン工業株式会社 | 新規α−フルオロメトキシカルボン酸エステル、該α−フルオロメトキシカルボン酸エステルの製造方法及びセボフルランの製造方法 |
| US9802954B2 (en) | 2011-08-24 | 2017-10-31 | Boehringer Ingelheim International Gmbh | Piperidino-dihydrothienopyrimidine sulfoxides and their use for treating COPD and asthma |
| CN108314624B (zh) * | 2017-01-17 | 2022-09-27 | 东莞东阳光科研发有限公司 | 一种多氟苯胺的制备方法 |
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| SE9903759D0 (sv) * | 1999-10-18 | 1999-10-18 | Astra Ab | Pharmaceutically active compounds |
| AR035216A1 (es) * | 2000-12-01 | 2004-05-05 | Astrazeneca Ab | Derivados de acido mandelico ,derivados farmaceuticamente aceptables, uso de estos derivados para la fabricacion de medicamentos, metodos de tratamiento ,procesos para la preparacion de estos derivados, y compuestos intermediarios |
-
2002
- 2002-05-31 SE SE0201662A patent/SE0201662D0/xx unknown
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2003
- 2003-05-16 TW TW092113322A patent/TW200307686A/zh unknown
- 2003-05-27 EP EP03756136A patent/EP1513807A1/en not_active Withdrawn
- 2003-05-27 BR BR0311138-5A patent/BR0311138A/pt not_active IP Right Cessation
- 2003-05-27 JP JP2004509650A patent/JP2005532345A/ja active Pending
- 2003-05-27 CN CNA038117347A patent/CN1656066A/zh active Pending
- 2003-05-27 CA CA002486110A patent/CA2486110A1/en not_active Abandoned
- 2003-05-27 MX MXPA04011910A patent/MXPA04011910A/es unknown
- 2003-05-27 PL PL03373409A patent/PL373409A1/xx not_active Application Discontinuation
- 2003-05-27 WO PCT/SE2003/000854 patent/WO2003101956A1/en not_active Ceased
- 2003-05-27 RU RU2004131868/15A patent/RU2004131868A/ru not_active Application Discontinuation
- 2003-05-27 AU AU2003232711A patent/AU2003232711A1/en not_active Abandoned
- 2003-05-27 US US10/516,426 patent/US20060052314A1/en not_active Abandoned
- 2003-05-28 AR ARP030101881A patent/AR040138A1/es not_active Application Discontinuation
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2004
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- 2004-11-11 IL IL16516904A patent/IL165169A0/xx unknown
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Also Published As
| Publication number | Publication date |
|---|---|
| BR0311138A (pt) | 2005-03-01 |
| CN1656066A (zh) | 2005-08-17 |
| IS7581A (is) | 2004-12-03 |
| CO5631429A2 (es) | 2006-04-28 |
| WO2003101956A1 (en) | 2003-12-11 |
| AU2003232711A1 (en) | 2003-12-19 |
| SE0201662D0 (sv) | 2002-05-31 |
| CA2486110A1 (en) | 2003-12-11 |
| JP2005532345A (ja) | 2005-10-27 |
| IL165169A0 (en) | 2005-12-18 |
| MXPA04011910A (es) | 2005-03-31 |
| ZA200408787B (en) | 2005-10-20 |
| EP1513807A1 (en) | 2005-03-16 |
| US20060052314A1 (en) | 2006-03-09 |
| NO20044673L (no) | 2004-12-07 |
| RU2004131868A (ru) | 2005-10-10 |
| TW200307686A (en) | 2003-12-16 |
| PL373409A1 (en) | 2005-08-22 |
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