AR046992A1 - Derivados de espiro-dihidrobenzofuranos - Google Patents
Derivados de espiro-dihidrobenzofuranosInfo
- Publication number
- AR046992A1 AR046992A1 ARP040104881A ARP040104881A AR046992A1 AR 046992 A1 AR046992 A1 AR 046992A1 AR P040104881 A ARP040104881 A AR P040104881A AR P040104881 A ARP040104881 A AR P040104881A AR 046992 A1 AR046992 A1 AR 046992A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- amino
- halogen
- alkoxy
- group
- Prior art date
Links
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 16
- 229910052736 halogen Inorganic materials 0.000 abstract 15
- 150000002367 halogens Chemical class 0.000 abstract 15
- -1 spiro dihydrobenzofuran derivatives Chemical class 0.000 abstract 13
- 125000001424 substituent group Chemical group 0.000 abstract 10
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 9
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 8
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract 7
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 abstract 6
- 125000000217 alkyl group Chemical group 0.000 abstract 5
- 229920006395 saturated elastomer Polymers 0.000 abstract 5
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 abstract 4
- 125000003545 alkoxy group Chemical group 0.000 abstract 4
- 125000004454 (C1-C6) alkoxycarbonyl group Chemical group 0.000 abstract 3
- 125000003341 7 membered heterocyclic group Chemical group 0.000 abstract 3
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 3
- 125000004122 cyclic group Chemical group 0.000 abstract 3
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 3
- 125000004916 (C1-C6) alkylcarbonyl group Chemical group 0.000 abstract 2
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 abstract 2
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 2
- 125000005842 heteroatom Chemical group 0.000 abstract 2
- 229910052760 oxygen Inorganic materials 0.000 abstract 2
- 229910052717 sulfur Inorganic materials 0.000 abstract 2
- 125000006700 (C1-C6) alkylthio group Chemical group 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
- 229910006074 SO2NH2 Inorganic materials 0.000 abstract 1
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 125000004043 oxo group Chemical group O=* 0.000 abstract 1
- UUEVFMOUBSLVJW-UHFFFAOYSA-N oxo-[[1-[2-[2-[2-[4-(oxoazaniumylmethylidene)pyridin-1-yl]ethoxy]ethoxy]ethyl]pyridin-4-ylidene]methyl]azanium;dibromide Chemical compound [Br-].[Br-].C1=CC(=C[NH+]=O)C=CN1CCOCCOCCN1C=CC(=C[NH+]=O)C=C1 UUEVFMOUBSLVJW-UHFFFAOYSA-N 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 239000012453 solvate Substances 0.000 abstract 1
- 125000005420 sulfonamido group Chemical group S(=O)(=O)(N*)* 0.000 abstract 1
- 238000002560 therapeutic procedure Methods 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/10—Spiro-condensed systems
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/10—Spiro-condensed systems
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- 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
- A61K31/403—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 condensed with carbocyclic rings, e.g. carbazole
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- 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
- A61K31/407—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 condensed with other heterocyclic ring systems, e.g. ketorolac, physostigmine
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- 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
- A61K31/438—The ring being spiro-condensed with carbocyclic or heterocyclic ring systems
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- Veterinary Medicine (AREA)
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- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
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- Endocrinology (AREA)
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- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
La presente se refiere a derivados de espiro-dihidrobenzofuranos, procesos para su preparacion, composiciones farmacéuticas que los contienen y su uso en terapia. Reivindicacion 1: Un compuesto caracterizado porque responde a la formula (1) donde m es 0, 1, 2, 3 o 4, donde cada R1 representa independientemente halogeno, ciano, hidroxilo, alquilo C1-6, haloalquilo C1-6, alcoxi C1-6, alquilsulfonilo C1-6 o sulfonamido (-SO2NH2); X representa una union o -CH2- e Y representa una union o -CH2-, siempre y cuando X e Y no representen ambos simultáneamente una union o -CH2-; n es 0, 1 o 2; donde cada R2 representa independientemente halogeno, alquilo C1-6 o haloalquilo C1-6; q es 0 o 1; p es 0 o 2; R3 representa un grupo que se selecciona entre halogeno, NR6R7, carboxilo o alquilo C1-6 donde dicho grupo alquilo C1-6 opcionalmente está sustituido por uno o más de halogeno, amino, hidroxilo, alcoxi C1-6, N-(C1-6alquil)amino, N,N-di-(C1-6 alquil)amino, carboxi o carbamoilo; R4 representa H, alquilo C1-6, haloalquilo C1-6 o halogeno; t es 0, 1 o 2, siempre y cuando p y t no sean ambos 0; R5 representa un sistema de anillo saturado o insaturado de entre 5 y 10 miembros donde dicho sistema de anillo puede comprender por lo menos un heteroátomo en el anillo que se selecciona entre N, O y S, donde el sistema de anillo está sustituido opcionalmente con uno o más sustituyentes que se seleccionan independientemente entre halogeno, ciano, oxo, nitro, hidroxilo, carboxilo, - C(O)H, -NR8R9, -C(O)NR10R11, -NHC(O)R12, -NHSO2R13, -SO2NR14R15, -NHC(O)NR16R17, un grupo que se selecciona entre alquilo C1-6, alquenilo C2-6, alquenilo C2-6, alcoxi C1-6, alquiltio C1-6, alquilsulfonilo C1-6, haloalquilo C1-6, alquilcarbonilo C1- 6, fenilcarbonilo, cicloalquilo C3-6, fenilo y un anillo heterocíclico saturado o insaturado de 5 o 6 miembros que comprende por lo menos un heteroátomo en el anillo que se selecciona entre N, O y S, donde cada grupo está sustituido opcionalmente con uno o más sustituyentes que se seleccionan independientemente entre halogeno, ciano, hidroxilo, carboxilo, alquilo C1-6, cicloalquilo C3-6, alcoxi C1-6 y alcoxicarbonilo C1-6, R6 y R7 representan cada uno independientemente H o un grupo que se selecciona entre alquilo C1-6 y alquilcarbonilo C1-6, cada uno de los cuales puede estar sustituido opcionalmente con uno o más sustituyentes que se seleccionan entre halogeno, amino, hidroxilo, alcoxi C1-6, N-(C1-6 alquil)amino, N,N-di-(C1-6 alquil)amino, carboxi, carbamoilo o alcoxicarbonilo C1-6, o R6 y R7 junto con el átomo de N al cual están unidos forman un anillo heterocíclico saturado de entre 4 y 7 miembros que puede estar sustituido opcionalmente con uno o más sustituyentes que se seleccionan entre halogeno, amino, hidroxilo, alcoxi C1-6, N-(C1-6 alquil)amino, N,N-di-(C1-6 alquil)amino, carboxi, carbamoilo o alcoxicarbonilo C1-6; R8, R9, R10, R11 representan cada uno independientemente H o un grupo que se selecciona entre alquilo C1-6 o cicloalquilo C3-6, donde cada grupo está sustituido opcionalmente con uno o más sustituyentes que se seleccionan independientemente entre halogeno, amino, hidroxilo, alcoxi C1-6, N-(C1-6 alquil)amino, N,N-di-(C1-6 alquil)amino, carboxi o carbamoilo; o R10 y R11, junto con el átomo de N al cual están unidos, forman un anillo heterocíclico saturado de entre 4 y 7 miembros que puede estar sustituido opcionalmente por lo menos con un sustituyente que se selecciona entre halogeno, amino, hidroxilo, alcoxi C1-6, N-(C1-6 alquil)amino, N,N-di-(C1-6 alquil)amino, carboxi, o carbamoilo; R12 representa H o un grupo que se selecciona entre alquilo C1-6 o cicloalquilo C3-6 donde cada grupo está sustituido opcionalmente con uno o más sustituyentes que se seleccionan independientemente entre halogeno, amino, hidroxilo, alcoxi C1-6, N-(C1-6 alquil)amino, N,N-di-(C1-6 alquil)amino, carboxi, o carbamoilo; R13 representa un grupo que se selecciona entre alquilo C1-6 o cicloalquilo C3-6, donde cada grupo está sustituido opcionalmente con uno o más sustituyentes que se seleccionan independientemente entre halogeno, amino, hidroxilo, alcoxi C1-6, N-(C1-6 alquil)amino, N,N-di-(C1-6 alquil)amino, carboxi, o carbamoilo; R14, R15, R16 y R17 representan cada uno independientemente H o un grupo que se selecciona entre alquilo C1-6 o cicloalquilo C3-6, donde cada grupo está sustituido opcionalmente con uno o más sustituyentes que se seleccionan independientemente entre halogeno, amino, hidroxilo, alcoxi C1-6, N-(C1-6 alquil)amino, N,N-di-(C1-6 alquil)amino, carboxi, o carbamoilo; o R14 y R15, o R16 y R17 junto con el átomo de N al cual están unidos forma cada uno independientemente un anillo heterocíclico saturado de entre 4 y 7 miembros que puede estar sustituido opcionalmente por lo menos con un sustituyente que se selecciona entre halogeno, amino, hidroxilo, alcoxi C1-6, N-(C1-6 alquil)amino, N,N-di-(C1-6 alquil)amino, carboxi, o carbamoilo; o una sal o solvato de los mismos aceptables para uso farmacéutico.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SE0303541A SE0303541D0 (sv) | 2003-12-22 | 2003-12-22 | New compounds |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR046992A1 true AR046992A1 (es) | 2006-01-04 |
Family
ID=30768856
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP040104881A AR046992A1 (es) | 2003-12-22 | 2004-12-22 | Derivados de espiro-dihidrobenzofuranos |
Country Status (17)
| Country | Link |
|---|---|
| US (2) | US7524856B2 (es) |
| EP (1) | EP1699791A1 (es) |
| JP (1) | JP2007515476A (es) |
| KR (1) | KR20060117343A (es) |
| CN (1) | CN1918160A (es) |
| AR (1) | AR046992A1 (es) |
| AU (1) | AU2004303735B2 (es) |
| BR (1) | BRPI0417036A (es) |
| CA (1) | CA2548494A1 (es) |
| IL (1) | IL175958A0 (es) |
| MX (1) | MXPA06007025A (es) |
| NO (1) | NO20063355L (es) |
| SE (1) | SE0303541D0 (es) |
| TW (1) | TW200604197A (es) |
| UY (1) | UY28694A1 (es) |
| WO (1) | WO2005061499A1 (es) |
| ZA (1) | ZA200605082B (es) |
Families Citing this family (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SE0202133D0 (sv) | 2002-07-08 | 2002-07-08 | Astrazeneca Ab | Novel compounds |
| US8017762B2 (en) | 2003-04-17 | 2011-09-13 | Alnylam Pharmaceuticals, Inc. | Modified iRNA agents |
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2003
- 2003-12-22 SE SE0303541A patent/SE0303541D0/xx unknown
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2004
- 2004-12-20 MX MXPA06007025A patent/MXPA06007025A/es unknown
- 2004-12-20 KR KR1020067012389A patent/KR20060117343A/ko not_active Withdrawn
- 2004-12-20 JP JP2006546906A patent/JP2007515476A/ja active Pending
- 2004-12-20 CN CNA200480042013XA patent/CN1918160A/zh active Pending
- 2004-12-20 BR BRPI0417036-9A patent/BRPI0417036A/pt not_active IP Right Cessation
- 2004-12-20 WO PCT/SE2004/001938 patent/WO2005061499A1/en not_active Ceased
- 2004-12-20 AU AU2004303735A patent/AU2004303735B2/en not_active Ceased
- 2004-12-20 CA CA002548494A patent/CA2548494A1/en not_active Abandoned
- 2004-12-20 EP EP04809111A patent/EP1699791A1/en not_active Withdrawn
- 2004-12-20 TW TW093139699A patent/TW200604197A/zh unknown
- 2004-12-20 US US10/583,468 patent/US7524856B2/en not_active Expired - Fee Related
- 2004-12-22 UY UY28694A patent/UY28694A1/es not_active Application Discontinuation
- 2004-12-22 AR ARP040104881A patent/AR046992A1/es unknown
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- 2006-05-25 IL IL175958A patent/IL175958A0/en unknown
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- 2006-07-19 NO NO20063355A patent/NO20063355L/no not_active Application Discontinuation
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2009
- 2009-04-28 US US12/431,338 patent/US20090298861A1/en not_active Abandoned
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| EP1699791A1 (en) | 2006-09-13 |
| US20070099945A1 (en) | 2007-05-03 |
| MXPA06007025A (es) | 2006-08-31 |
| TW200604197A (en) | 2006-02-01 |
| CA2548494A1 (en) | 2005-07-07 |
| AU2004303735B2 (en) | 2007-09-20 |
| UY28694A1 (es) | 2005-07-29 |
| SE0303541D0 (sv) | 2003-12-22 |
| NO20063355L (no) | 2006-09-22 |
| ZA200605082B (en) | 2007-11-28 |
| US20090298861A1 (en) | 2009-12-03 |
| CN1918160A (zh) | 2007-02-21 |
| US7524856B2 (en) | 2009-04-28 |
| WO2005061499A1 (en) | 2005-07-07 |
| BRPI0417036A (pt) | 2007-02-06 |
| IL175958A0 (en) | 2006-10-05 |
| KR20060117343A (ko) | 2006-11-16 |
| JP2007515476A (ja) | 2007-06-14 |
| AU2004303735A1 (en) | 2005-07-07 |
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