AR079492A1 - Moduladores de crth2 - Google Patents
Moduladores de crth2Info
- Publication number
- AR079492A1 AR079492A1 ARP100104664A ARP100104664A AR079492A1 AR 079492 A1 AR079492 A1 AR 079492A1 AR P100104664 A ARP100104664 A AR P100104664A AR P100104664 A ARP100104664 A AR P100104664A AR 079492 A1 AR079492 A1 AR 079492A1
- Authority
- AR
- Argentina
- Prior art keywords
- ring
- halogen
- independently selected
- instances
- independently
- Prior art date
Links
- 102000009389 Prostaglandin D receptors Human genes 0.000 title abstract 3
- 108050000258 Prostaglandin D receptors Proteins 0.000 title abstract 3
- 229910052736 halogen Inorganic materials 0.000 abstract 21
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 18
- 150000002367 halogens Chemical class 0.000 abstract 18
- 125000000623 heterocyclic group Chemical group 0.000 abstract 11
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 10
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 9
- 125000003118 aryl group Chemical group 0.000 abstract 7
- 125000001072 heteroaryl group Chemical group 0.000 abstract 7
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 7
- 125000002950 monocyclic group Chemical group 0.000 abstract 6
- 229910052757 nitrogen Inorganic materials 0.000 abstract 6
- 125000001313 C5-C10 heteroaryl group Chemical group 0.000 abstract 5
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 5
- 125000002619 bicyclic group Chemical group 0.000 abstract 5
- 125000001931 aliphatic group Chemical group 0.000 abstract 4
- 125000005843 halogen group Chemical group 0.000 abstract 4
- 125000005842 heteroatom Chemical group 0.000 abstract 4
- 229910052760 oxygen Inorganic materials 0.000 abstract 4
- 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 abstract 3
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract 3
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 abstract 3
- 125000003545 alkoxy group Chemical group 0.000 abstract 3
- 125000004429 atom Chemical group 0.000 abstract 3
- 150000001875 compounds Chemical class 0.000 abstract 3
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 abstract 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 3
- 125000006574 non-aromatic ring group Chemical group 0.000 abstract 3
- 229910052717 sulfur Inorganic materials 0.000 abstract 3
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 2
- 125000006645 (C3-C4) cycloalkyl group Chemical group 0.000 abstract 2
- 125000006570 (C5-C6) heteroaryl group Chemical group 0.000 abstract 2
- 125000000217 alkyl group Chemical group 0.000 abstract 2
- 229910052799 carbon Inorganic materials 0.000 abstract 2
- 229910052739 hydrogen Inorganic materials 0.000 abstract 2
- 239000001257 hydrogen Substances 0.000 abstract 2
- 125000004435 hydrogen atom Chemical class [H]* 0.000 abstract 2
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 abstract 2
- 125000001557 phthalyl group Chemical group C(=O)(O)C1=C(C(=O)*)C=CC=C1 0.000 abstract 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 2
- 150000003839 salts Chemical class 0.000 abstract 2
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 abstract 1
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 1
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 abstract 1
- 125000001999 4-Methoxybenzoyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1OC([H])([H])[H])C(*)=O 0.000 abstract 1
- 125000006163 5-membered heteroaryl group Chemical group 0.000 abstract 1
- YZCKVEUIGOORGS-OUBTZVSYSA-N Deuterium Chemical compound [2H] YZCKVEUIGOORGS-OUBTZVSYSA-N 0.000 abstract 1
- KCNKJCHARANTIP-SNAWJCMRSA-N allyl-{4-[3-(4-bromo-phenyl)-benzofuran-6-yloxy]-but-2-enyl}-methyl-amine Chemical group C=1OC2=CC(OC/C=C/CN(CC=C)C)=CC=C2C=1C1=CC=C(Br)C=C1 KCNKJCHARANTIP-SNAWJCMRSA-N 0.000 abstract 1
- 239000005557 antagonist Substances 0.000 abstract 1
- 208000006673 asthma Diseases 0.000 abstract 1
- 125000000043 benzamido group Chemical group [H]N([*])C(=O)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 abstract 1
- SYGWYBOJXOGMRU-UHFFFAOYSA-N chembl233051 Chemical group C1=CC=C2C3=CC(C(N(CCN(C)C)C4=O)=O)=C5C4=CC=CC5=C3SC2=C1 SYGWYBOJXOGMRU-UHFFFAOYSA-N 0.000 abstract 1
- 229910052805 deuterium Inorganic materials 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 125000004438 haloalkoxy group Chemical group 0.000 abstract 1
- 125000005347 halocycloalkyl group Chemical group 0.000 abstract 1
- -1 or alternatively Chemical compound 0.000 abstract 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 abstract 1
- JUJWROOIHBZHMG-UHFFFAOYSA-N pyridine Substances C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 abstract 1
- 208000023504 respiratory system disease Diseases 0.000 abstract 1
- 125000006413 ring segment Chemical group 0.000 abstract 1
- 125000000446 sulfanediyl group Chemical group *S* 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
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- 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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- 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
- A61K31/4025—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 not condensed and containing further heterocyclic rings, e.g. cromakalim
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- C07D207/325—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms with substituted hydrocarbon radicals directly attached to the ring nitrogen atom
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Abstract
Se divulgan los moduladores de CRTH2, particularmente los antagonistas de CRTH2, que son utiles para tratar varios trastornos, incluyendo el asma y los trastornos respiratorios. Reivindicacion 1: Un compuesto de formula (1) o una sal farmacéuticamente aceptable del mismo; con la condicion de que el compuesto de formula (1) no es un compuesto seleccionado de ácido 5-[[6-metoxi-3-(4-metoxibenzoíl)-2-metil-1H-pirrol[2,3-b]piridin-1-il]metil]-a,a-dimetil-2H-tetrazol-2-acético [ns de registro CAS 1097838-63-5], ácido 5-[[5-(benzoílamino)-2-tiazolil]tio]-2H-tetrazol-2-acético [ns de registro CAS 1099441-56-1], ácido 2-butil-1-[[4-[(2-carboxibenzoíl)amino]fenil]metil]-5-cloro-1H-imidazol-4-acético [ns de registro CAS 114798-40-2], y ácido 2-butil-1-[[4-[(2-carboxibenzoíl)amino]fenil]metil]-5-cloro-1H-imidazol-4-acético [ns de registro CAS 114773-45-4], o una sal farmacéuticamente aceptable de los mismos; en donde: el anillo A es un anillo monocíclico o bicíclico seleccionado de arilo de 6 a 10 miembros, heteroarilo de 5 a 10 miembros, cicloalifático C3-10 y heterociclo de 4 a 10 miembros; en donde dicho heteroarilo o heterociclo contiene entre 0 y 3 heteroátomos del anillo independientemente seleccionados de N, O y S; el anillo B es un anillo monocíclico seleccionado de fenilo y heteroarilo de 5 a 6 miembros en donde dicho heteroarilo contiene hasta tres heteroátomos del anillo independientemente seleccionados de N, O y S; el anillo D es un heteroarilo de 5 miembros; en donde x1 se selecciona de N y C; x2 se selecciona de N y C-R2; x3 se selecciona de N y C; x4 se selecciona de N y C-R4; y x5 se selecciona de N y C-R5; siempre que al menos uno de x1 o x3 sea N, pero ambos al mismo no sean simultáneamente N; R2 se selecciona de -H, halogeno, -NO2, -CN, radical C1-6 alifático, alcoxi C1-6 y un anillo ciclopropilo, en donde R2 está independientemente sustituido con entre 0 y 3 instancias de RA; en donde cada RA está independientemente seleccionado de halogeno, -OH, alcoxi C1-2 y haloalcoxi C1-2; R4 se selecciona a partir de halogeno, -NO2, -CN, -R6, -OR6, -C(O)R6, -C(O)OR6, -N(R6)2, -S(O)pR6, -S(O)2N(R6)2, -NR6S(O)2R6, -C(O)N(R6)2 y -NR6C(O)R6; R5 se selecciona a partir de halogeno, -NO2, -CN, -R6, -OR6, -C(O)R6, -C(O)OR6, -N(R6)2, -S(O)pR6, -S(O)2N(R6)2, -NR6S(O)2R6, -C(O)N(R6)2 y -NR6C(O)R6; p es un entero seleccionado de 0, 1 y 2; cada R6 se selecciona independientemente de -H, un radical C1-6 alifático y un anillo monocíclico o bicíclico; en donde el anillo se selecciona de arilo de 6 a 10 miembros, heteroarilo de 5 a 10 miembros, cicloalifático C3-10 y heterociclo de 4 a 10 miembros; donde cuando R6 es un radical C1-6 alifático, está independientemente sustituido con entre 0 y 6 instancias de R7, cuando R6 es un anillo no aromático o un heteroarilo, está independientemente sustituido con entre 0 y 6 instancias de R8, y cuando R6 es un arilo, está independientemente sustituido con entre 0 y 6 instancias de R8'; cada R7 se selecciona independientemente a partir de halogeno, -CN, oxo, -OR9, -R10, -C(O)R9, -C(O)OR9, -S(O)mR9, -N(R9)2, -S(O)2N(R9)2, -NR9S(O)2R9, -C(O)N(R9)2 y -NR9C(O)R9; cada R8 se selecciona independientemente a partir de halogeno, -CN, -NO2, oxo, radical alifático C1-6, -R10, -C(O)R9, -C(O)OR9, -OR9, -S(O)mR9, -N(R9)2, -S(O)2N(R9)2, -NR9S(O)2R9, -C(O)N(R9)2 y -NR9C(O)R9; cada R8' se selecciona independientemente de halogeno, -CN, -NO2, radical alifático C1-6, -R10, -C(O)R9, -C(O)OR9, -OR9, -S(O)mR9, -N(R9)2, -S(O)2N(R9)2, -NR9S(O)2R9, -C(O)N(R9)2 y -NR9C(O)R9; cada R9 se selecciona independientemente de hidrogeno, radical alifático C1-6 y un anillo monocíclico o bicíclico; en donde el anillo se selecciona de arilo de 6 a 10 miembros, heteroarilo de, 5 a 10 miembros, cicloalifático C3-10 y heterociclo de 4 a 10 miembros; en donde cuando R9 es un radical alifático C1-6, está independientemente sustituido con entre 0 y 6 instancias de R11 y cuando R9 es un anillo, está independientemente sustituido con entre 0 y 3 instancias de R12; cada R10 es un anillo monocíclico o bicíclico independientemente seleccionado de arilo de 6 a 10 miembros, heteroarilo de 5 a 10 miembros, cicloalifático C3-10 y heterociclo de 4 a 10 miembros; y cada R10 está independientemente sustituido con entre 0 y 3 instancias de R12; cada R11 está independientemente seleccionado de halogeno, -CN, -OH, alcoxi C1-4 y haloalcoxi C1-4; cada R12 está independientemente seleccionado de halogeno, -CN, -OH, alcoxi C1-4, haloalcoxi C1-4, alcoxi C1-4, y haloalcoxi C1-4; R13 se selecciona de -H, radical alifático C1-6 y un anillo monocíclico o bicíclico donde el anillo se selecciona de arilo de 6 a 10 miembros, heteroarilo de 5 a 10 miembros, cicloalifático C3-10 y heterociclo de 4 a 10 miembros; donde cuando R13 es un radical alifático C1-6, está independientemente sustituido con entre 0 y 6 instancias de R14, cuando R13 es un anillo no aromático o un heteroarilo, está independientemente sustituido con entre 0 y 6 instancias de R15, y cuando R13 es un arilo, está independientemente sustituido con entre 0 y 6 instancias de R15'; cada R14 se selecciona independientemente a partir de halogeno, -CN, oxo, -OR9, -R10, -C(O)R9, -C(O)OR9, -S(O)mR9, -N(R9)2, -S(O)2N(R9)2, -NR9S(O)2R9, -C(O)N(R9)2 y -NR9C(O)R9; cada R15 se selecciona independientemente a partir de halogeno, -CN, -NO2, oxo, radical alifático C1-6, -R10, -C(O)R9, -C(O)OR9, -OR9, -S(O)mR9, -N(R9)2, -S(O)2N(R9)2, -NR9S(O)2R9, -C(O)N(R9)2 y -NR9C(O)R9; y R15' se selecciona independientemente de halogeno, -CN, -NO2, radical alifático C1-6, -R10, -C(O)R9, -C(O)OR9, -OR9, -S(O)mR9, -N(R9)2, -S(O)2N(R9)2, -NR9S(O)2R9, -C(O)N(R9)2 y -NR9C(O)R9; R16 y R17 están independientemente seleccionados de -H, deuterio, alquilo C1-6, haloalquilo C1-6, y halogeno, o alternativamente, R16 y R17 están independientemente seleccionados de alquilo C1-4 y haloalquilo C1-6, y R16 y R17 tomados en conjunto con el átomo al que están unidos forman un anillo ciclopropilo y halociclopropilo; L es un enlace seleccionado de metileno, -C(O)-, -O-, S(O)m y -NR1-; en donde cuando L es un metileno, está independientemente sustituido con entre 0 y 2 instancias de R18; m es 0, 1 o 2; R1 está seleccionado de -H, radical alifático C1-6, cicloalifático C3-6, -CO(alifático C1-6), -CO(cicloalifático C3-6), -CO-(fenilo), bencilo y -CO-(bencilo); en donde cuando R1 está seleccionado de radical alifático C1-6, -CO-(fenilo), bencilo y -CO-(bencilo), está independientemente sustituido de entre 0 y 3 instancias de RB; en donde cada RB está independientemente seleccionado de halogeno, alquilo C1-2 alcoxi C1-2; cada R18 está independientemente seleccionado de halogeno, -CN, radical alifático C1-6, radical haloalifático C1-6, y cicloalifático C3-6; o alternativamente, cada R18 está independientemente seleccionado de radical alifático C1-6 y radical haloalifático C1-6, y dos grupos R18 tomados en conjunto con el átomo al que están unidos forman un anillo ciclopropilo y halociclopropilo; o es un entero seleccionado de 0, 1 y 2; cada JB está independientemente seleccionado de halogeno, -NO2, -CN, -R19, -C(O)H, -C(O)OH, -C(O)NH2, -OH, -SH, -NH2,-C(O)R19, -C(O)OR19, -C(O)N(R20)R19, -N(R20)C(O)R19, -OR19, -SR19 y-NR19R20; o alternativamente, dos grupos JB unidos a dos anillos vecinos de los átomos del anillo B, junto con dichos átomos del anillo, forman un heterociclo de 5 a 6 miembros o un heteroarilo de 5 a 6 miembros, cada uno de los anillos esta independientemente sustituido con entre 0 y 2 instancias de RE, en donde cada RE está independientemente seleccionado de halogeno, alquilo C1-2, alcoxi C1-2, -CN y -OH; cada R20 está independientemente seleccionado de -H y un radical alifático C1-6; cada R19 está independientemente seleccionado de radical alifático C1-6, cicloalifático C3-6, fenilo, bencilo, heterociclo de 4 a 6 miembros y heteroarilo de 5 a 6 miembros; en donde cuando R19 es un radical alifático C1-6, está independientemente sustituido con entre 0 y 3 instancias de RC, donde cada RC está independientemente seleccionado de halogeno, -CN, -OH, -NH2, cicloalquilo C3-4, halocicloalquilo C3-4, -O(alquilo C1-4), -O(cicloalquilo C3-4), -O(halocicloalquilo C3-4), -O(haloalquilo C1-4), -NH(alquilo C1-4), -N(alquilo C1-4)2, y -NRV; en donde -NRV es un heterociclo de 4 a 6 miembros que contiene un átomo del anillo N ligado a JB, y en donde dicho heterociclo contiene de 0 a 2 heteroátomos adicionales del anillo seleccionados a partir de O y N; cuando R19 es un heterociclo o un heteroarilo, contiene de 1 a 3 heteroátomos del anillo seleccionados independientemente a partir de N, O y S; cuando R19 es fenilo, está independientemente sustituido con entre 0 y 3 instancias de RD, donde cada RD está independientemente seleccionado de halogeno, radical alifático C1-4, -CN, -OH, -NH2, -O(alquilo C1-4), -NH(alquilo C1-4) y -N(alquilo C1-4)2; en donde cuando R19 es un anillo no aromático o un heteroarilo, está independientemente sustituido con entre 0 y 3 instancias de RD', donde cada RD' está independientemente seleccionado de halogeno, oxo, radical alifático C1-4, -CN, -OH, -NH2, -O(alquilo C1-4), -NH(alquilo C1-4) y -N(alquilo C1-4)2; en donde L' es un enlace seleccionado de -Y-SO2-, -NR21SO2-, -SO2NR21-, -Y-C(O)-, -NR21C(O)- y -C(O)NR21-; en donde Y está seleccionado de un enlace simple, un enlace recto de alquileno C1-2 y un enlace ramificado de alquileno C2, en donde el enlace alquileno C1-2 está independientemente sustituido con entre 0 y 3 átomos de halogeno; R21 está seleccionado de hidrogeno, alquilo C1-6, haloalquilo C1-6, y anillo cicloalquilo C3-6; n es un entero seleccionado de 0, 1, 2 y 3; cada JA está independientemente seleccionado de halogeno, -NO2, -CN, -R22, -C(O)H, -C(O)OH, -C(O)NH2, -OH, -SH, y -NH2, -C(O)R22, -C(O)OR22, -C(O)N(R23)R22, -N(R23)C(O)R22, -OR22, -SR22 y -NR22R23; cada R23 está independientemente seleccionado de -H y un radical alifático C1-6; cada R22 está independientemente seleccionado de radical alifático C1-4, anillo c
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ECSP12011996A (es) | 2012-10-30 |
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MX2012007239A (es) | 2012-10-15 |
CR20120343A (es) | 2013-01-25 |
BR112012017756A2 (pt) | 2016-04-19 |
CN102822163B (zh) | 2016-01-20 |
KR20120098908A (ko) | 2012-09-05 |
CL2012001712A1 (es) | 2012-12-07 |
UY33110A (es) | 2011-07-29 |
TW201130810A (en) | 2011-09-16 |
EA201200855A1 (ru) | 2013-04-30 |
AU2010333829A1 (en) | 2012-07-12 |
WO2011079007A1 (en) | 2011-06-30 |
ZA201204527B (en) | 2013-09-25 |
EP2516416A1 (en) | 2012-10-31 |
CN102822163A (zh) | 2012-12-12 |
US8674115B2 (en) | 2014-03-18 |
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