ES8802151A1 - Un procedimiento para la preparacion de nuevos piridazinaminas. - Google Patents
Un procedimiento para la preparacion de nuevos piridazinaminas.Info
- Publication number
- ES8802151A1 ES8802151A1 ES556738A ES556738A ES8802151A1 ES 8802151 A1 ES8802151 A1 ES 8802151A1 ES 556738 A ES556738 A ES 556738A ES 556738 A ES556738 A ES 556738A ES 8802151 A1 ES8802151 A1 ES 8802151A1
- Authority
- ES
- Spain
- Prior art keywords
- aryl
- substituted
- 6alkyl
- compounds
- pyridazines
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
Classifications
-
- 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
- C07D401/04—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 directly linked by a ring-member-to-ring-member bond
-
- 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
- C07D403/04—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 directly linked by a ring-member-to-ring-member bond
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/04—Centrally acting analgesics, e.g. opioids
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D237/00—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings
- C07D237/02—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings
- C07D237/06—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
- C07D237/10—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D237/20—Nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D237/00—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings
- C07D237/02—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings
- C07D237/06—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
- C07D237/10—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D237/22—Nitrogen and oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
Abstract
PROCEDIMIENTO PARA LA PREPARACION DE PIRIDAZINAMINAS, DE FORMULA GENERAL (I), CON FORMA N-OXIDO, UNA SAL DE ADICION DE ACIDO FARMACEUTICAMENTE ACEPTABLE O UNA FORMA ESTEROQUIMICAMENTE ISOMERICA DEL MISMO. CONSISTE EN SOMETER A REACCION DE N-ALQUILACION UNA AMINA DE FORMULA GENERAL (II), CON UN REACTIVO DE FORMULA GENERAL (III), EN LAS QUE M ES 2 O 3; R1, R2, R3 Y R4 SON CADA UNO DE ELLOS INDEPENDIENTEMENTE HIDROGENO O ALQUILO C1-6; R5 ES (ARIL) ALQUENILO C2-6 O (ARIL) ALQUINILO C2-6; R ES HIDROGENO, HALO, HIDROXI O FENILO; Y W REPRESENTA UN GRUPO SALIENTE REACTIVO, TAL COMO HALOGENO O SULFONILOXI. DICHA REACCION SE EFECTUA EN PRESENCIA DE UN DISOLVENTE ORGANICO. DE APLICACION EN MEDICINA PARA PREVENIR Y COMBATIR EL DOLOR EN ANIMALES DE SANGRE CALIENTE.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US76084585A | 1985-07-31 | 1985-07-31 |
Publications (2)
Publication Number | Publication Date |
---|---|
ES556738A0 ES556738A0 (es) | 1988-04-01 |
ES8802151A1 true ES8802151A1 (es) | 1988-04-01 |
Family
ID=25060338
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ES556738A Expired ES8802151A1 (es) | 1985-07-31 | 1986-06-25 | Un procedimiento para la preparacion de nuevos piridazinaminas. |
Country Status (18)
Country | Link |
---|---|
EP (1) | EP0211457A3 (es) |
JP (1) | JPS6229575A (es) |
KR (1) | KR870001192A (es) |
CN (1) | CN86105558A (es) |
AU (1) | AU6073986A (es) |
DK (1) | DK363186A (es) |
ES (1) | ES8802151A1 (es) |
FI (1) | FI863120A (es) |
GR (1) | GR862022B (es) |
HU (1) | HU195501B (es) |
IL (1) | IL79549A0 (es) |
NO (1) | NO863083L (es) |
NZ (1) | NZ216918A (es) |
PH (1) | PH22884A (es) |
PT (1) | PT83098B (es) |
TN (1) | TNSN86117A1 (es) |
ZA (1) | ZA865700B (es) |
ZW (1) | ZW14886A1 (es) |
Families Citing this family (34)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
MY104343A (en) * | 1987-11-23 | 1994-03-31 | Janssen Pharmaceutica Nv | Novel pyridizinamine deravatives |
US4992433A (en) * | 1987-11-23 | 1991-02-12 | Janssen Pharmaceutica N.V. | Novel pyridazinamine derivatives |
GB8911158D0 (en) * | 1989-05-16 | 1989-07-05 | Janssen Pharmaceutica Nv | Antiviral pyridazinamines |
US5070090A (en) * | 1989-05-15 | 1991-12-03 | Janssen Pharmaceutica N.V. | Antipicorpaviral herterocyclic-substituted morpholinyl alkylphenol ethers |
US5270312A (en) * | 1990-11-05 | 1993-12-14 | Warner-Lambert Company | Substituted piperazines as central nervous system agents |
DK1027336T3 (da) * | 1997-10-27 | 2005-01-24 | Neurosearch As | Heteroaryldiazacycloalkaner, deres fremstilling og anvendelse |
CN1348449A (zh) | 1999-04-26 | 2002-05-08 | 神经研究公司 | 杂芳基二氮杂环烷烃及其制备方法和应用 |
EP1430033A4 (en) | 2001-08-31 | 2004-12-15 | Univ Northwestern | PROTEIN KINASE ANTI-INFLAMMATORY AND INHIBITOR COMPOSITION AND METHOD OF USE |
US7390813B1 (en) | 2001-12-21 | 2008-06-24 | Xenon Pharmaceuticals Inc. | Pyridylpiperazines and aminonicotinamides and their use as therapeutic agents |
US7759348B2 (en) | 2003-07-30 | 2010-07-20 | Xenon Pharmaceuticals Inc. | Pyridazine derivatives and their use as therapeutic agents |
BRPI0412343A (pt) * | 2003-07-30 | 2006-09-05 | Xenon Pharmaceuticals Inc | derivados de piridazina e seu uso como agentes terapêuticos |
US7754711B2 (en) * | 2003-07-30 | 2010-07-13 | Xenon Pharmaceuticals Inc. | Pyridazine derivatives and their use as therapeutic agents |
EP2316827B1 (en) | 2003-07-30 | 2016-01-27 | Xenon Pharmaceuticals Inc. | Piperazine derivatives and their use as therapeutic agents |
EP2269610A3 (en) | 2004-09-20 | 2011-03-09 | Xenon Pharmaceuticals Inc. | Heterocyclic derivatives and their use as stearoyl-coa desaturase inhibitors |
MX2007003318A (es) | 2004-09-20 | 2007-05-18 | Xenon Pharmaceuticals Inc | Derivados heterociclicos y su uso como agentes terapeuticos. |
MX2007003327A (es) | 2004-09-20 | 2007-06-05 | Xenon Pharmaceuticals Inc | Derivados heterociclicos, y su uso como mediadores de estearoil-coa desaturasa. |
CN101084207A (zh) | 2004-09-20 | 2007-12-05 | 泽农医药公司 | 杂环衍生物及其作为硬脂酰CoA去饱和酶抑制剂的用途 |
BRPI0515488A (pt) | 2004-09-20 | 2008-07-29 | Xenon Pharmaceuticals Inc | derivados de heterocìclicos e seu uso como agentes terapêuticos |
CA2580845A1 (en) | 2004-09-20 | 2006-03-30 | Xenon Pharmaceuticals Inc. | Pyridazine derivatives for inhibiting human stearoyl-coa-desaturase |
AU2005286647A1 (en) | 2004-09-20 | 2006-03-30 | Xenon Pharmaceuticals Inc. | Heterocyclic derivatives and their use as stearoyl-CoA desaturase inhibitors |
CN101087766B (zh) | 2004-11-02 | 2011-09-07 | 西北大学 | 哒嗪化合物、组合物和方法 |
EP1812007B1 (en) | 2004-11-02 | 2011-09-07 | Northwestern University | Pyridazine compounds and methods |
AU2016203312B2 (en) * | 2004-11-02 | 2018-05-24 | Centre National De La Recherche Scientifique | Pyridazine compounds, compositions and methods |
JP2009513563A (ja) | 2005-06-03 | 2009-04-02 | ゼノン・ファーマシューティカルズ・インコーポレイテッド | ヒトのステアロイル−CoAデサチュラーゼ阻害剤としてのアミノチアゾール誘導体 |
JO2769B1 (en) | 2005-10-26 | 2014-03-15 | جانسين فارماسوتيكا ان. في | Rapid decomposition of physiologically antagonistic agents of the 2-dopamine receptor |
CA2650711A1 (en) | 2006-04-28 | 2007-11-08 | Northwestern University | Compositions and treatments using pyridazine compounds and cholinesterase inhibitors |
JP2009535344A (ja) | 2006-04-28 | 2009-10-01 | ノースウェスタン ユニバーシティ | 神経炎症性疾患の処置のためのピリダジン化合物を含む処方物 |
JO2849B1 (en) | 2007-02-13 | 2015-03-15 | جانسين فارماسوتيكا ان. في | Dopamine 2 receptor antagonists are rapidly hydrolyzed |
KR101506156B1 (ko) | 2007-04-23 | 2015-03-26 | 얀센 파마슈티카 엔.브이. | 속해리성 도파민 2 수용체 길항제로서의 티아(디아)졸 |
ES2393818T3 (es) | 2007-04-23 | 2012-12-28 | Janssen Pharmaceutica, N.V. | Derivados de tipo 4-alcoxipiridazina como antagonistas de los receptores 2 de la dopamina de disociación rápida |
WO2008145681A2 (en) * | 2007-05-31 | 2008-12-04 | Boehringer Ingelheim International Gmbh | Ccr2 receptor antagonists and uses thereof |
CN102171189B (zh) | 2008-07-31 | 2013-11-20 | 詹森药业有限公司 | 作为快速解离多巴胺2受体拮抗剂的哌嗪-1-基-三氟甲基取代的吡啶 |
WO2012159662A1 (en) * | 2011-05-24 | 2012-11-29 | Universita' Degli Studi Di Bari | New 1-arylpiperazinic ligands of 5-ht7 receptor and use thereof |
BR112017028492B1 (pt) | 2015-07-02 | 2023-12-26 | Centrexion Therapeutics Corporation | Citrato de (4-((3r,4r)-3-metoxitetra-hidro-piran-4- ilamino)piperidin-1-il) (5- metil-6-(((2r, 6s)-6-(p-tolil) tetra-hidro-2h-piran-2-il)metilamino)pirimidin-4-il) metanona, seu uso e seu método de preparação, e composição farmacêutica |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2985657A (en) * | 1959-10-12 | 1961-05-23 | Paul A J Janssen | 1-(aroylalkyl)-4-heterocyclylpiperazines |
US5001125A (en) * | 1984-03-26 | 1991-03-19 | Janssen Pharmaceutica N.V. | Anti-virally active pyridazinamines |
-
1986
- 1986-06-25 ES ES556738A patent/ES8802151A1/es not_active Expired
- 1986-07-09 EP EP86201203A patent/EP0211457A3/en not_active Withdrawn
- 1986-07-14 KR KR1019860005671A patent/KR870001192A/ko not_active Application Discontinuation
- 1986-07-21 NZ NZ216918A patent/NZ216918A/xx unknown
- 1986-07-23 JP JP61171940A patent/JPS6229575A/ja active Pending
- 1986-07-28 CN CN198686105558A patent/CN86105558A/zh active Pending
- 1986-07-28 PH PH34070A patent/PH22884A/en unknown
- 1986-07-29 TN TNTNSN86117A patent/TNSN86117A1/fr unknown
- 1986-07-29 IL IL79549A patent/IL79549A0/xx unknown
- 1986-07-30 ZA ZA865700A patent/ZA865700B/xx unknown
- 1986-07-30 DK DK363186A patent/DK363186A/da not_active Application Discontinuation
- 1986-07-30 ZW ZW148/86A patent/ZW14886A1/xx unknown
- 1986-07-30 GR GR862022A patent/GR862022B/el unknown
- 1986-07-30 PT PT83098A patent/PT83098B/pt unknown
- 1986-07-30 FI FI863120A patent/FI863120A/fi not_active IP Right Cessation
- 1986-07-30 NO NO863083A patent/NO863083L/no unknown
- 1986-07-30 HU HU863248A patent/HU195501B/hu unknown
- 1986-07-31 AU AU60739/86A patent/AU6073986A/en not_active Abandoned
Also Published As
Publication number | Publication date |
---|---|
CN86105558A (zh) | 1987-01-28 |
IL79549A0 (en) | 1986-10-31 |
ZA865700B (en) | 1988-03-30 |
DK363186A (da) | 1987-02-01 |
KR870001192A (ko) | 1987-03-12 |
HU195501B (en) | 1988-05-30 |
PT83098B (en) | 1988-07-13 |
FI863120A (fi) | 1987-02-01 |
AU6073986A (en) | 1987-02-05 |
JPS6229575A (ja) | 1987-02-07 |
ES556738A0 (es) | 1988-04-01 |
HUT41772A (en) | 1987-05-28 |
FI863120A0 (fi) | 1986-07-30 |
ZW14886A1 (en) | 1988-02-24 |
NZ216918A (en) | 1988-11-29 |
PH22884A (en) | 1989-01-19 |
EP0211457A2 (en) | 1987-02-25 |
NO863083D0 (no) | 1986-07-30 |
NO863083L (no) | 1987-02-02 |
EP0211457A3 (en) | 1987-07-22 |
GR862022B (en) | 1986-12-24 |
TNSN86117A1 (fr) | 1990-01-01 |
PT83098A (en) | 1986-08-01 |
DK363186D0 (da) | 1986-07-30 |
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