AR036132A1 - Pirazinas, formulacion farmaceutica, uso de estos compuestos en la fabricacion de medicamentos, procesos para la preparacion de estos compuestos e intermediarios - Google Patents
Pirazinas, formulacion farmaceutica, uso de estos compuestos en la fabricacion de medicamentos, procesos para la preparacion de estos compuestos e intermediariosInfo
- Publication number
- AR036132A1 AR036132A1 ARP020102533A ARP020102533A AR036132A1 AR 036132 A1 AR036132 A1 AR 036132A1 AR P020102533 A ARP020102533 A AR P020102533A AR P020102533 A ARP020102533 A AR P020102533A AR 036132 A1 AR036132 A1 AR 036132A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- nr6r7
- nr1r2
- alkynyl
- cycloalkyl
- Prior art date
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- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/24—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D213/36—Radicals substituted by singly-bound nitrogen atoms
- C07D213/42—Radicals substituted by singly-bound nitrogen atoms having hetero atoms attached to the substituent nitrogen atom
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- A61P17/14—Drugs for dermatological disorders for baldness or alopecia
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- C07C233/77—Carboxylic acid amides having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by amino groups
- C07C233/78—Carboxylic acid amides having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by amino groups with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by an acyclic carbon atom
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- C07C311/15—Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings
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- C07C311/22—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound oxygen atoms
- C07C311/29—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound oxygen atoms having the sulfur atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring
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- C07C311/50—Compounds containing any of the groups, X being a hetero atom, Y being any atom
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- C07D207/04—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 no double bonds between ring members or between ring members and non-ring members
- C07D207/08—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 no double bonds between ring members or between ring members and non-ring members with hydrocarbon radicals, substituted by hetero atoms, attached to ring carbon atoms
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Abstract
Pirazinas que tienen la fórmula (1) en donde: Z es CH o N; Y es CONR5, NR5CO, SO2NR5, NR5SO2, CH2NR5, NR5CH2, NR5CONR5, alquileno C1-6, CH2CO, COCH2, CH=CH, OCH2 o CH2O; X es CH o N; P es fenilo o un anillo heteroaromático de 5 o 6 miembros que contiene uno o más heteroátomos seleccionados entre N, O ó S, y dicho anillo fenilo o anillo heteroaromático de 5 o 6 miembros puede opcionalmente estar fusionado con un anillo de 5 o 6 miembros saturado, parcialmente saturado o insaturado que contiene uno o más átomo seleccionados entre C, N, O ó S; Q es fenilo o un anillo heteroaromático de 5 o 6 miembros que contiene uno o más heteroátomos seleccionados entre N, O ó S, de los cuales por lo menos un átomo se selecciona entre nitrógeno; R es CHO, fluormetoxi, difluormetoxi, trifluormetoxi, alquilo C0-6(SO2)NR1R2, O alquilo C0-6(SO2)NR1R2, O alquilo C1-6(SO)NR1R2, alquilo C1-6(SO)NR1R2, alquilo C0-6NR1(SO)R2, O alquilo C1-6NR1(SO)R2, alquilo C0-6NR1(SO2)NR1R2, O alquilo C1-6 NR1(SO2)R2, alquilo C0-6 (SO2) alquilo C1-6NR1R2, O alquilo C0-6(SO2)alquilo C1-6 NR1R2, alquilo C0-6(SO)alquilo C1-6 NR1R2, O alquilo C1-6 (SO) alquilo C1-6NR1R2, alquilo C0-6 S alquilo C1-6 NR1R2, O alquilo C1-6 S alquilo C1-6 NR1R2, O alquilo C1-6 O alquilo C1-6, alquilo C1-6 O alquilo C1-6 NR1R2, O alquilo C1-6 O alquilo C1-6 NR1R2, alquilo C0-6 CONR10R11, O alquilo C0-6 CONR1R2, O alquilo C1-6 NR1R2, alquilo C0-6NR10 (CO)R11, O alquilo C1-6 NR1(CO)R2, alquilo C0-6NR11(CO)R10, alquilo C0-6COR11, O alquilo C1-6 COR1, alquilo C0-6NR10R11, alquilo C0-6 O(CO)R11, O alquilo C1-6 O (CO)R1, alquilo C0-6 C(NR10)NR10R11, alquilo C0-6C(NR11)N(R10)2, O alquilo C0-6 C(NR1)NR1R2, alquilo C0-6NR10(CO)OR11, O alquilo C1-6NR1(CO)OR2, alquilo C0-6NR11(CO)OR10, O alquilo C1-6 CN, NR1OR2, alquilo C0-6 (CO)OR8, O alquilo C1-6(CO)OR1, NR1 (CO)NR1R2, NR1(CO)(CO)R2, NR1(CO)(CO)NR1R2, OR12, ó SO3R1; R1 y R2 se seleccionan de manera independiente entre hidrógeno, alquilo C1-6, alquenilo C2-6, alquinilo C2-6, alquilo C0-6 cicloalquilo C3-6, (CO)OR8, alquilheterocicloalquilo C0-6, alquilo C1-6 NR6R7, alquilarilo C0-6 y alquilheteroarilo C0-6, en donde cualquier de alquilo C1-6, alquenilo C2-6, alquinilo C2-6, alquilo C0-6 cicloalquilo C3-6, alquilheterocicloalquilo C0-6, alquilarilo C0-6, alquilheteroarilo C0-6 puede estar sustituido con uno o más A; R1 y R2 pueden formar juntos un anillo heterocíclico de 5, 6 o 7 miembros sustituido que contiene uno o más heteroátomos seleccionados entre N, O ó S, cuyo anillo heterocíclico puede estar opcionalmente sustituido con A; R3 y R4 se seleccionan de manera independiente entre halo, nitro, CHO, alquilo C0-6CN, O alquilo C1-6 CN, alquilo C0-6OR6, O alquilo C1-6 OR6, fluormetilo, difluormetilo, trifluormetilo, fluormetoxi, difluormetoxi, trifluormetoxi, alquilo C0-6 NR6R7, O alquilo C1-6 NR6R7, O alquilo C1-6 O alquilo C1-6 NR6R7, NR6OR7 alquilo C0-6 CO2R6, O alquilo C1-6 CO2R6, alquilo C0-6 CONR6R7, O alquilo C1-6 CONR6R7, O alquilo C1-6 NR6(CO)R7, alquilo C0-6 NR6(CO)R7, O(CO)NR6R7, NR6(CO)OR7, NR6(CO)NR6R7, O(CO)OR6, O(CO)R6, alquilo C0-6COR6, O alquilo C1-6 COR6, NR6(CO)(CO)R6, NR6(CO)(CO)NR6R7, SR6, alquilo C0-6 (SO2)NR6R7, O alquilo C1-6 NR6(SO2)R7, O alquilo C0-6 (SO2)NR6R7, alquilo C0-6 (SO)NR6R7, O alquilo C1-6 (SO)NR6R7, SO3R6, alquilo C0-6NR6(SO2)NR6R7, alquilo C0-6NR6(SO)R7, O alquilo C1-6 NR6(SO)R7, O alquilo C0-6 SO2R6, alquilo C0-6SO2R6, alquilo C0-6SOR6, alquilo C1-6, alquenilo C2-6, alquinilo C2-6, alquilo C0-6 cicloalquilo C3-6, alquilarilo C0-6 y alquilheteroarilo C0-6, en donde cualquiera de alquilo C1-6, alquenilo C2-6, alquinilo C2-6, alquilo C0-6 cicloalquilo C3-6, alquilarilo C0-6 y alquilheteroarilo C0-6 puede estar opcionalmente sustituido con uno o más A; m es 0, 1, 2, 3 o 4; n es 0, 1, 2, 3 ó 4; R5 es hidrógeno, alquilo C1-6, alquenilo C2-6, alquinilo C2-6, alquilo C0-6 cicloalquilo C3-6, alquilarilo C0-6 y alquilheteroarilo C0-6, alquilo C1-6 NR6R7 o alquilo C1-6 CONR6R7; R6 y R7 se seleccionan de manera independiente entre hidrógeno, alquilo C1-6, (CO)OR8, alquenilo C2-6, alquinilo C2-6, alquilo C0-6 cicloalquilo C3-6, alquilarilo C0-6 y alquilheteroarilo C0-6 y alquilo C1-6 NR8R9; R6 y R7 pueden formar juntos un anillo heterocíclico de 5 o 6 miembros sustituido, que contiene uno o más heteroátomos seleccionados entre N, O ó S, cuyo anillo heterocíclico puede estar opcionalmente sustituido con A; R8 y R9 se seleccionan de manera independiente entre hidrógeno, alquilo C1-6, alquenilo C2-6, alquinilo C2-6, alquilo C0-6 cicloalquilo C3-6, alquilarilo C0-6 y alquilheteroarilo C0-6; R8 y R9 pueden formar juntos un anillo heterocíclico de 5 o 6 miembros que contiene uno o más heteroátomos seleccionados entre N, O ó S, cuyo anillo heterocíclico puede estar opcionalmente sustituido con A, R10 es hidrógeno, alquilo C1-6, alquenilo C2-6, alquinilo C2-6, alquilo C0-6 cicloalquilo C3-6, alquilarilo C0-6 y alquilheteroarilo C0-6 o alquilo C1-6 NR8R9; R11 es alquilo C1-6 NR8R9 o alquilheterocicloalquilo C0-6; R10 y R11 pueden formar juntos un anillo heterocíclico de 5, 6 o 7 miembros que contiene uno o más heteroátomos seleccionados entre N, O ó S, cuyo anillo heterocíclico puede estar opcionalmente sustituido con A; R12 es un anillo heterocíclico de 5, 6 o 7 miembros que contiene uno o más heteroátomos seleccionados entre N, O ó S, cuyo anillo heterocíclico puede estar opcionalmente sustituido con A; en donde cualquiera de alquilo C1-6, alquenilo C2-6, alquinilo C2-6, alquilo C0-6 cicloalquilo C3-6, alquilheterocicloalquilo C0-6, alquilarilo C0-6, alquilheteroarilo C0-6 definidos en R5 a R12 pueden estar sustituidos con uno o más A; A es halo, nitro, CHO, CN, OR6, alquilo C1-6, alquenilo C2-6, alquinilo C2-6, alquilo C0-6 cicloalquilo C3-6, fluormetilo, difluormetilo, trifluormetilo, fluormetoxi, difluormetoxi, trifluormetoxi, alquilo C0-6NR6R7, O alquilo C1-6, NR6R7, CO2R8, CONR6R7, NR6(CO)R6, O(CO)R6, COR6, SR6, (SO2)NR6R7, (SO)NR6R7, SO3R6, SO2R6 ó SOR6, como una base libre o como una sal farmacéuticamente aceptable de la misma, con la condición de que el compuesto no es 4[4-[5-amino-6-(fenilmetil)pirazinil]fenoxi]-etil éster del ácido butanoico; formulación farmacéutica, uso de estos compuestos en la fabricación de medicamentos procesos para la preparación de estos compuestos e intermediarios. Estos compuestos son útiles en terapia, especialmente en la prevención y/o el tratamiento de condiciones asociadas con glucógeno sintasa quinasa -3(GSK3).
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
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| SE0102439A SE0102439D0 (sv) | 2001-07-05 | 2001-07-05 | New compounds |
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| AR036132A1 true AR036132A1 (es) | 2004-08-11 |
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| ARP020102533A AR036132A1 (es) | 2001-07-05 | 2002-07-05 | Pirazinas, formulacion farmaceutica, uso de estos compuestos en la fabricacion de medicamentos, procesos para la preparacion de estos compuestos e intermediarios |
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| US (1) | US20060052396A1 (es) |
| EP (1) | EP1414801A1 (es) |
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| IL (1) | IL159347A0 (es) |
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| MX (1) | MXPA03011972A (es) |
| NO (1) | NO20040014L (es) |
| PL (1) | PL367782A1 (es) |
| RU (1) | RU2004102389A (es) |
| SE (1) | SE0102439D0 (es) |
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| RU2736219C2 (ru) | 2014-06-17 | 2020-11-12 | Вертекс Фармасьютикалз Инкорпорейтед | Способ лечения рака с использованием комбинации ингибиторов снк1 и atr |
| EP3741375A1 (en) | 2014-07-17 | 2020-11-25 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Methods for treating neuromuscular junction-related diseases |
| JO3589B1 (ar) * | 2014-08-06 | 2020-07-05 | Novartis Ag | مثبطات كيناز البروتين c وطرق استخداماتها |
| WO2016207366A1 (en) | 2015-06-26 | 2016-12-29 | INSERM (Institut National de la Santé et de la Recherche Médicale) | Methods and pharmaceutical compositions for the treatment of viral infections |
| AU2016331955B2 (en) | 2015-09-30 | 2022-07-21 | Vertex Pharmaceuticals Incorporated | Method for treating cancer using a combination of DNA damaging agents and ATR inhibitors |
| GB201519573D0 (en) | 2015-11-05 | 2015-12-23 | King S College London | Combination |
| CN108697811B (zh) | 2016-01-11 | 2023-04-07 | 梅里麦克制药股份有限公司 | 抑制共济失调毛细血管扩张和Rad3相关蛋白(ATR) |
| WO2017216342A1 (en) | 2016-06-16 | 2017-12-21 | Ecole Polytechnique Federale De Lausanne (Epfl) | Method for preparing induced hepatic progenitor cells |
| DK3971177T3 (da) | 2016-07-20 | 2024-07-15 | Novartis Ag | Aminopyridin-derivater og anvendelse deraf som selektive ALK-2-inhibitorer |
| TW201811766A (zh) | 2016-08-29 | 2018-04-01 | 瑞士商諾華公司 | N-(吡啶-2-基)吡啶-磺醯胺衍生物及其用於疾病治療之用途 |
| JP2022520671A (ja) | 2019-02-08 | 2022-03-31 | フリークエンシー・セラピューティクス・インコーポレイテッド | 耳障害を治療するためのバルプロ酸化合物及びwnt作動薬 |
| CN115038443A (zh) | 2019-11-22 | 2022-09-09 | 因西特公司 | 包含alk2抑制剂和jak2抑制剂的组合疗法 |
| WO2021257532A1 (en) | 2020-06-16 | 2021-12-23 | Incyte Corporation | Alk2 inhibitors for the treatment of anemia |
| WO2022031946A1 (en) | 2020-08-06 | 2022-02-10 | Chdi Foundation, Inc. | Heterobiaryl compounds and imaging agents for imaging huntingtin protein |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5547004A (en) * | 1992-01-28 | 1996-08-20 | Klockner Hansel Tevopharm B.V. | Method and device for arranging a stream of products |
| MA26473A1 (fr) * | 1997-03-01 | 2004-12-20 | Glaxo Group Ltd | Composes pharmacologiquement actifs. |
| NZ520484A (en) * | 2000-02-16 | 2005-03-24 | Neurogen Corp | Substituted arylpyrazines that are modulators of CRF (corticotropin releasing factor) receptor and methods of treatment using them |
| AR029489A1 (es) * | 2000-03-10 | 2003-07-02 | Euro Celtique Sa | Piridinas, pirimidinas, pirazinas, triazinas sustituidas por arilo, composiciones farmaceuticas y el uso de las mismas para la manufactura de un medicamento |
-
2001
- 2001-07-05 SE SE0102439A patent/SE0102439D0/xx unknown
-
2002
- 2002-07-03 PL PL02367782A patent/PL367782A1/xx not_active Application Discontinuation
- 2002-07-03 RU RU2004102389/04A patent/RU2004102389A/ru not_active Application Discontinuation
- 2002-07-03 CA CA002452686A patent/CA2452686A1/en not_active Abandoned
- 2002-07-03 CN CNA028135458A patent/CN1551869A/zh active Pending
- 2002-07-03 EP EP02747795A patent/EP1414801A1/en not_active Withdrawn
- 2002-07-03 KR KR10-2004-7000080A patent/KR20040013102A/ko not_active Withdrawn
- 2002-07-03 HU HU0500339A patent/HUP0500339A2/hu unknown
- 2002-07-03 JP JP2003510640A patent/JP2005505515A/ja active Pending
- 2002-07-03 US US10/481,721 patent/US20060052396A1/en not_active Abandoned
- 2002-07-03 WO PCT/SE2002/001339 patent/WO2003004472A1/en not_active Ceased
- 2002-07-03 MX MXPA03011972A patent/MXPA03011972A/es unknown
- 2002-07-03 IL IL15934702A patent/IL159347A0/xx unknown
- 2002-07-03 BR BR0210838-0A patent/BR0210838A/pt not_active Application Discontinuation
- 2002-07-05 AR ARP020102533A patent/AR036132A1/es unknown
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2003
- 2003-12-23 ZA ZA200309977A patent/ZA200309977B/xx unknown
- 2003-12-30 CO CO03113306A patent/CO5540341A2/es not_active Application Discontinuation
- 2003-12-31 IS IS7095A patent/IS7095A/is unknown
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2004
- 2004-01-02 NO NO20040014A patent/NO20040014L/no not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| KR20040013102A (ko) | 2004-02-11 |
| SE0102439D0 (sv) | 2001-07-05 |
| MXPA03011972A (es) | 2004-03-26 |
| CN1551869A (zh) | 2004-12-01 |
| BR0210838A (pt) | 2004-07-13 |
| EP1414801A1 (en) | 2004-05-06 |
| WO2003004472A8 (en) | 2003-03-13 |
| US20060052396A1 (en) | 2006-03-09 |
| JP2005505515A (ja) | 2005-02-24 |
| PL367782A1 (en) | 2005-03-07 |
| NO20040014L (no) | 2004-03-02 |
| CA2452686A1 (en) | 2003-01-16 |
| ZA200309977B (en) | 2005-03-23 |
| WO2003004472A1 (en) | 2003-01-16 |
| HUP0500339A2 (hu) | 2005-07-28 |
| IS7095A (is) | 2003-12-31 |
| RU2004102389A (ru) | 2005-07-10 |
| CO5540341A2 (es) | 2005-07-29 |
| IL159347A0 (en) | 2004-06-01 |
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