AR093036A1 - Derivados de pirrolotriazinona como inhibidores de pi3k - Google Patents
Derivados de pirrolotriazinona como inhibidores de pi3kInfo
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- AR093036A1 AR093036A1 ARP130103757A ARP130103757A AR093036A1 AR 093036 A1 AR093036 A1 AR 093036A1 AR P130103757 A ARP130103757 A AR P130103757A AR P130103757 A ARP130103757 A AR P130103757A AR 093036 A1 AR093036 A1 AR 093036A1
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- Prior art keywords
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- phenyl
- heteroatom selected
- branched
- Prior art date
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- 239000012828 PI3K inhibitor Substances 0.000 title 1
- 229940043441 phosphoinositide 3-kinase inhibitor Drugs 0.000 title 1
- 125000001072 heteroaryl group Chemical group 0.000 abstract 14
- 125000005842 heteroatom Chemical group 0.000 abstract 14
- 229910052757 nitrogen Inorganic materials 0.000 abstract 14
- 229910052760 oxygen Inorganic materials 0.000 abstract 14
- 229910052717 sulfur Inorganic materials 0.000 abstract 14
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 13
- 125000002853 C1-C4 hydroxyalkyl group Chemical group 0.000 abstract 10
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 10
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract 9
- 125000000217 alkyl group Chemical group 0.000 abstract 9
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 abstract 8
- 125000005843 halogen group Chemical group 0.000 abstract 8
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 8
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 7
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 7
- 125000002950 monocyclic group Chemical group 0.000 abstract 7
- 125000001424 substituent group Chemical group 0.000 abstract 7
- 125000002619 bicyclic group Chemical group 0.000 abstract 6
- 125000000623 heterocyclic group Chemical group 0.000 abstract 6
- 125000006645 (C3-C4) cycloalkyl group Chemical group 0.000 abstract 4
- 125000006272 (C3-C7) cycloalkyl group Chemical group 0.000 abstract 3
- 108091007960 PI3Ks Proteins 0.000 abstract 2
- 102000003993 Phosphatidylinositol 3-kinases Human genes 0.000 abstract 2
- 108090000430 Phosphatidylinositol 3-kinases Proteins 0.000 abstract 2
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 1
- 125000006650 (C2-C4) alkynyl group Chemical group 0.000 abstract 1
- 125000006717 (C3-C10) cycloalkenyl group Chemical group 0.000 abstract 1
- 125000006376 (C3-C10) cycloalkyl group Chemical group 0.000 abstract 1
- 125000006708 (C5-C14) heteroaryl group Chemical group 0.000 abstract 1
- 150000001204 N-oxides Chemical class 0.000 abstract 1
- 125000000304 alkynyl group Chemical group 0.000 abstract 1
- 125000002618 bicyclic heterocycle group Chemical group 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 125000000392 cycloalkenyl group Chemical group 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- 125000001188 haloalkyl group Chemical group 0.000 abstract 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 abstract 1
- 239000003112 inhibitor Substances 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- BEBRHYJBTAMGRW-UHFFFAOYSA-N pyrrolo[3,2-d]triazin-4-one Chemical class O=C1N=NN=C2C=CN=C12 BEBRHYJBTAMGRW-UHFFFAOYSA-N 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 239000000126 substance Substances 0.000 abstract 1
- 238000002560 therapeutic procedure Methods 0.000 abstract 1
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-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
- A61K31/53—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with three nitrogens as the only ring hetero atoms, e.g. chlorazanil, melamine
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Abstract
Se describen derivados de pirrolotriazinona que tienen la estructura química de fórmula (1); así como un procedimiento para su preparación, composiciones farmacéuticas que los contienen y su uso en terapia como inhibidores de fosfoinositido 3-quinasas (PI3Ks). Reivindicación 1: Un compuesto de fórmula (1), o una sal farmacéuticamente aceptable, o N-óxido, o derivado isotópicamente marcado del mismo; en donde, n representa 0, 1, 2 ó 3; cada uno de Rᵃ y Rᵇ independientemente representa un átomo de hidrógeno, un grupo haloalquilo C₁₋₄, un grupo hidroxialquilo C₁₋₄ o un grupo alquilo lineal o ramificado C₁₋₄; R¹ representa un grupo cicloalquilo C₃₋₁₀, un grupo cicloalquenilo C₃₋₁₀, un grupo fenilo, un grupo heteroarilo de 5 a 7 miembros que contiene al menos un heteroátomo seleccionado de O, S y N, o un grupo heterociclilo de 5 a 7 miembros que contiene al menos un heteroátomo seleccionado de O, S y N, en donde los grupos cicloalquilo, cicloalquenilo, fenilo, heteroarilo y heterociclilo están no sustituidos o sustituidos con uno o más sustituyentes seleccionados de un átomo de halógeno, un grupo hidroxilo, un grupo ciano, un grupo alquilo lineal o ramificado C₁₋₄, un grupo haloalquilo C₁₋₄, un grupo hidroxialquilo C₁₋₄, un grupo cicloalquilo C₃₋₄; cada uno de R² y R³ independientemente representa un átomo de hidrógeno, un átomo de halógeno, un grupo hidroxilo, un grupo ciano, un grupo alquilo lineal o ramificado C₁₋₄, un grupo haloalquilo C₁₋₄, un grupo hidroxialquilo C₁₋₄, un grupo cicloalquilo C₃₋₄, un grupo alcoxi C₁₋₄, un grupo -NH₂, un grupo -N(CH₃)H o un grupo -N(CH₃)₂; cada uno de R⁷ y R⁸ independientemente representa un átomo de hidrógeno, un grupo haloalquilo C₁₋₄, un grupo hidroxialquilo C₁₋₄ o un grupo alquilo lineal o ramificado C₁₋₄; y a) R⁴ representa un átomo de hidrógeno, un grupo alcoxi C₁₋₄, un grupo haloalquilo C₁₋₄, un grupo hidroxialquilo C₁₋₄, un grupo cicloalquilo C₃₋₇, un grupo -(CH₂)₀₋₃-S-(CH₂)₀₋₃-(grupo fenilo), un grupo -(CH₂)₀₋₃-S-(CH₂)₀₋₃-(grupo heteroarilo monocíclico o bicíclico de 5 a 14 miembros que contiene al menos un heteroátomo seleccionado de O, S y N), un grupo -(CH₂)₀₋₃-O-(CH₂)₀₋₃-(grupo fenilo), un grupo -(CH₂)₀₋₃-O-(CH₂)₀₋₃-(grupo heteroarilo monocíclico o bicíclico de 5 a 14 miembros que contiene al menos un heteroátomo seleccionado de O, S y N), un grupo -(CH₂)₀₋₃-(grupo fenilo), un grupo -(CH₂)₀₋₃-(grupo heteroarilo monocíclico o bicíclico de 5 a 14 miembros que contiene al menos un heteroátomo seleccionado de O, S y N), o un grupo alquilo lineal o ramificado C₁₋₄, donde dicho grupo alquilo está no sustituido o sustituido con uno o más sustituyentes seleccionados de un grupo alcoxi C₁₋₄, un grupo ciano, un grupo cicloalquilo C₃₋₄, un grupo -C(O)-(CH₂)₀₋₃-R⁸ o un grupo -C(O)-(CH₂)₀₋₃-NR⁷R⁸; en donde los grupos fenilo y heteroarilo están no sustituidos o sustituidos con uno o más sustituyentes seleccionados de un átomo de halógeno, un grupo hidroxilo, un grupo ciano, un grupo alquilo lineal o ramificado C₁₋₄, un grupo haloalquilo C₁₋₄, un grupo hidroxialquilo C₁₋₄ o un grupo alcoxi C₁₋₄; R⁶ representa un átomo de hidrógeno; un átomo de halógeno; un grupo hidroxilo; un grupo ciano; un grupo alcoxi C₁₋₄; un grupo haloalquilo C₁₋₄; un grupo hidroxialquilo lineal o ramificado C₁₋₄; un grupo cicloalquilo C₃₋₇; un grupo -(CH₂)₀₋₃NR⁷R⁸; un grupo -(CH₂)₁₋₃-O(grupo alquilo C₁₋₄); un grupo -(CH₂)₀₋₃-OC(O)-(grupo alquilo C₁₋₄); un grupo -(CH₂)₀₋₃-C(O)O-(grupo alquilo C₁₋₄); un grupo -C(O)-(CH₂)₀₋₃-NR⁷R⁸; un grupo -(CH₂)₀₋₃-C(O)OH; un grupo -(CH₂)₀₋₃-S-(CH₂)₀₋₃-(grupo fenilo), un grupo -(CH₂)₀₋₃-S-(CH₂)₀₋₃-(grupo heteroarilo monocíclico o bicíclico de 5 a 14 miembros que contiene al menos un heteroátomo seleccionado de O, S y N), un grupo -(CH₂)₀₋₃-O-(CH₂)₀₋₃-(grupo fenilo), un grupo -(CH₂)₀₋₃-O-(CH₂)₀₋₃-(grupo heteroarilo monocíclico o bicíclico de 5 a 14 miembros que contiene al menos un heteroátomo seleccionado de O, S y N); un grupo -(CH₂)₀₋₃-(grupo fenilo); un grupo -(CH₂)₀₋₃-(grupo heteroarilo monocíclico o bicíclico de 5 a 14 miembros que contiene al menos un heteroátomo seleccionado de O, S y N); un grupo -(CH₂)₀₋₃-(grupo heterociclilo monocíclico o bicíclico de 5 a 14 miembros que contiene al menos un heteroátomo seleccionado de O, S y N); un grupo alquinilo C₂₋₄ o un grupo alquilo lineal o ramificado C₁₋₄, donde dicho grupo alquilo está no sustituido o sustituido con uno o más sustituyentes seleccionados de un grupo alcoxi C₁₋₄, un grupo ciano o un grupo cicloalquilo C₃₋₄; en donde los grupos fenilo, heteroarilo, heterociclilo y alquinilo están no sustituidos o sustituidos con uno o más sustituyentes seleccionados de un átomo de halógeno, un grupo hidroxilo, un grupo ciano, un grupo alquilo lineal o ramificado C₁₋₄, un grupo haloalquilo C₁₋₄, un grupo hidroxialquilo C₁₋₄, un grupo alcoxi C₁₋₄, un grupo -(CH₂)₀₋₃-NR⁷-(CH₂)₀₋₃-NR⁷R⁸, un grupo -(CH₂)₀₋₃-C(O)-(CH₂)₀₋₃-(grupo heteroarilo de 5 a 7 miembros que contiene al menos un heteroátomo seleccionado de O, S y N) o un grupo -(CH₂)₀₋₃-(grupo heterociclilo de 5 a 7 miembros que contiene al menos un heteroátomo seleccionado de O, S y N); en donde los grupos heteroarilo y heterociclilo están no sustituidos o sustituidos con uno o más sustituyentes seleccionados de un átomo de halógeno, un grupo hidroxilo, un grupo ciano, un grupo alquilo lineal o ramificado C₁₋₄, un grupo haloalquilo C₁₋₄, un grupo hidroxialquilo C₁₋₄, un grupo alcoxi C₁₋₄; R⁵ representa un resto de fórmula (2), (3), (4) ó (5) en donde: cada uno de R⁹, R¹¹, R¹³, R¹⁴ y R¹⁵ independientemente representa un átomo de hidrógeno, un grupo -(CH₂)₀₋₃CN, un grupo -(CH₂)₀₋₃NRR, o un grupo alquilo lineal o ramificado C₁₋₄ en donde cada uno de R y R independientemente representa un átomo de hidrógeno, un grupo hidroxilo, un grupo alcoxi C₁₋₄, un grupo hidroxialquilo C₁₋₄ o un grupo alquilo lineal o ramificado C₁₋₄; cada uno de R¹⁰ y R¹² independientemente representa un grupo fenilo, o un grupo heteroarilo de 5 a 14 miembros que contiene al menos un heteroátomo seleccionado de O, S y N, en donde los grupos fenilo y heteroarilo están no sustituidos o sustituidos con uno o más sustituyentes seleccionados de un átomo de halógeno, un grupo hidroxilo, un grupo ciano, un grupo alquilo lineal o ramificado C₁₋₆, un grupo haloalquilo C₁₋₄, un grupo hidroxialquilo lineal o ramificado C₁₋₆, un grupo cicloalquilo C₃₋₇, un grupo -(CH₂)₀₋₃-(grupo fenilo), un grupo -(CH₂)₀₋₃-(grupo heteroarilo de 5 a 14 miembros que contiene al menos un heteroátomo seleccionado de O, S y N), un grupo -(CH₂)₀₋₃-(un grupo heterociclilo de 5 a 14 miembros que contiene al menos un heteroátomo seleccionado de O, S y N), un grupo -(CH₂)₁₋₃CN, un grupo -(CH₂)₀₋₃-O-(CH₂)₀₋₃-R, un grupo -C(O), un grupo -(CH₂)₀₋₃NRR, un grupo -(CH₂)₀₋₃-C(O)-(CH₂)₁₋₃-CN, un grupo -(CH₂)₀₋₃NC(O)OH, un grupo -(CH₂)₀₋₃-C(O)-(CH₂)₀₋₃-R, un grupo -(CH₂)₀₋₃-C(O)-(CH₂)₀₋₃-NRR, un grupo -(CH₂)₀₋₃NR-C(O)-(CH₂)₀₋₃-NRR, un grupo -(CH₂)₀₋₃NR-C(O)-(CH₂)₀₋₃-R, un grupo -(CH₂)₀₋₃NR-S(O)₂-(CH₂)₀₋₃-R, un grupo
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP12382399 | 2012-10-16 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR093036A1 true AR093036A1 (es) | 2015-05-13 |
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP130103757A AR093036A1 (es) | 2012-10-16 | 2013-10-16 | Derivados de pirrolotriazinona como inhibidores de pi3k |
Country Status (29)
| Country | Link |
|---|---|
| US (1) | US9388189B2 (es) |
| EP (1) | EP2909207A1 (es) |
| JP (1) | JP2015533181A (es) |
| KR (1) | KR20150068953A (es) |
| CN (1) | CN104854108A (es) |
| AP (1) | AP2015008328A0 (es) |
| AR (1) | AR093036A1 (es) |
| AU (1) | AU2013333938A1 (es) |
| BR (1) | BR112015007231A2 (es) |
| CA (1) | CA2883426A1 (es) |
| CL (1) | CL2015000956A1 (es) |
| CR (1) | CR20150175A (es) |
| DO (1) | DOP2015000077A (es) |
| EA (1) | EA027277B1 (es) |
| GE (1) | GEP201706623B (es) |
| GT (1) | GT201500094A (es) |
| HK (1) | HK1211027A1 (es) |
| IL (1) | IL237475A0 (es) |
| MD (1) | MD20150048A2 (es) |
| MX (1) | MX2015004327A (es) |
| NI (1) | NI201500054A (es) |
| PE (1) | PE20150637A1 (es) |
| PH (1) | PH12015500813A1 (es) |
| SG (1) | SG11201502032VA (es) |
| TN (1) | TN2015000112A1 (es) |
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| UY (1) | UY35086A (es) |
| WO (1) | WO2014060432A1 (es) |
| ZA (1) | ZA201501220B (es) |
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| CN108290896B (zh) * | 2015-11-16 | 2021-09-28 | 托帕杜制药公司 | 2-苯基-3,4-二氢吡咯并[2,1-f][1,2,4]三嗪酮衍生物及其用途 |
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- 2013-10-15 CA CA2883426A patent/CA2883426A1/en not_active Abandoned
- 2013-10-15 EA EA201500426A patent/EA027277B1/ru not_active IP Right Cessation
- 2013-10-15 EP EP13779788.2A patent/EP2909207A1/en not_active Withdrawn
- 2013-10-15 PE PE2015000410A patent/PE20150637A1/es not_active Application Discontinuation
- 2013-10-15 AU AU2013333938A patent/AU2013333938A1/en not_active Abandoned
- 2013-10-15 GE GEAP201313828A patent/GEP201706623B/en unknown
- 2013-10-15 KR KR1020157009063A patent/KR20150068953A/ko not_active Withdrawn
- 2013-10-15 MX MX2015004327A patent/MX2015004327A/es unknown
- 2013-10-15 BR BR112015007231A patent/BR112015007231A2/pt not_active IP Right Cessation
- 2013-10-15 CN CN201380065926.2A patent/CN104854108A/zh active Pending
- 2013-10-15 AP AP2015008328A patent/AP2015008328A0/xx unknown
- 2013-10-15 SG SG11201502032VA patent/SG11201502032VA/en unknown
- 2013-10-15 JP JP2015537230A patent/JP2015533181A/ja not_active Withdrawn
- 2013-10-15 US US14/435,851 patent/US9388189B2/en not_active Expired - Fee Related
- 2013-10-15 HK HK15111815.3A patent/HK1211027A1/xx unknown
- 2013-10-15 WO PCT/EP2013/071551 patent/WO2014060432A1/en not_active Ceased
- 2013-10-16 UY UY0001035086A patent/UY35086A/es not_active Application Discontinuation
- 2013-10-16 AR ARP130103757A patent/AR093036A1/es unknown
- 2013-10-16 TW TW102137293A patent/TW201429975A/zh unknown
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2015
- 2015-02-23 ZA ZA2015/01220A patent/ZA201501220B/en unknown
- 2015-02-26 IL IL237475A patent/IL237475A0/en unknown
- 2015-03-24 TN TNP2015000112A patent/TN2015000112A1/fr unknown
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- 2015-03-30 DO DO2015000077A patent/DOP2015000077A/es unknown
- 2015-04-13 PH PH12015500813A patent/PH12015500813A1/en unknown
- 2015-04-15 CL CL2015000956A patent/CL2015000956A1/es unknown
- 2015-04-16 GT GT201500094A patent/GT201500094A/es unknown
- 2015-04-16 NI NI201500054AA patent/NI201500054A/es unknown
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| TN2015000112A1 (en) | 2016-06-29 |
| CR20150175A (es) | 2015-05-11 |
| US9388189B2 (en) | 2016-07-12 |
| KR20150068953A (ko) | 2015-06-22 |
| SG11201502032VA (en) | 2015-05-28 |
| EA201500426A1 (ru) | 2015-10-30 |
| HK1211027A1 (en) | 2016-05-13 |
| AP2015008328A0 (en) | 2015-03-31 |
| GT201500094A (es) | 2017-08-01 |
| GEP201706623B (en) | 2017-02-10 |
| CL2015000956A1 (es) | 2015-06-19 |
| AU2013333938A1 (en) | 2015-04-09 |
| BR112015007231A2 (pt) | 2017-07-04 |
| CA2883426A1 (en) | 2014-04-24 |
| PE20150637A1 (es) | 2015-05-08 |
| CN104854108A (zh) | 2015-08-19 |
| JP2015533181A (ja) | 2015-11-19 |
| US20150291595A1 (en) | 2015-10-15 |
| UY35086A (es) | 2014-05-30 |
| PH12015500813B1 (en) | 2015-06-08 |
| IL237475A0 (en) | 2015-04-30 |
| PH12015500813A1 (en) | 2015-06-08 |
| TW201429975A (zh) | 2014-08-01 |
| ZA201501220B (en) | 2017-04-26 |
| EP2909207A1 (en) | 2015-08-26 |
| EA027277B1 (ru) | 2017-07-31 |
| MD20150048A2 (ro) | 2015-10-31 |
| NI201500054A (es) | 2016-02-01 |
| DOP2015000077A (es) | 2015-04-30 |
| MX2015004327A (es) | 2015-06-10 |
| WO2014060432A1 (en) | 2014-04-24 |
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