AR099789A1 - Derivados de 8-(piperazin-1-il)-1,2,3,4-tetrahidro-isoquinolina - Google Patents

Derivados de 8-(piperazin-1-il)-1,2,3,4-tetrahidro-isoquinolina

Info

Publication number
AR099789A1
AR099789A1 ARP150100819A ARP150100819A AR099789A1 AR 099789 A1 AR099789 A1 AR 099789A1 AR P150100819 A ARP150100819 A AR P150100819A AR P150100819 A ARP150100819 A AR P150100819A AR 099789 A1 AR099789 A1 AR 099789A1
Authority
AR
Argentina
Prior art keywords
alkyl
heteroaryl
aryl
phenyl
independently selected
Prior art date
Application number
ARP150100819A
Other languages
English (en)
Original Assignee
Actelion Pharmaceuticals Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Actelion Pharmaceuticals Ltd filed Critical Actelion Pharmaceuticals Ltd
Publication of AR099789A1 publication Critical patent/AR099789A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic 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
    • C07D471/02Heterocyclic 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
    • C07D471/04Ortho-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic 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
    • A61K31/47Quinolines; Isoquinolines
    • A61K31/472Non-condensed isoquinolines, e.g. papaverine
    • A61K31/4725Non-condensed isoquinolines, e.g. papaverine containing further heterocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/496Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • A61P11/06Antiasthmatics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00Drugs for disorders of the urinary system
    • A61P13/10Drugs for disorders of the urinary system of the bladder
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00Drugs for disorders of the urinary system
    • A61P13/12Drugs for disorders of the urinary system of the kidneys
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • A61P19/02Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/14Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/28Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • A61P37/02Immunomodulators
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • A61P37/02Immunomodulators
    • A61P37/06Immunosuppressants, e.g. drugs for graft rejection
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/10Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic 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
    • C07D401/14Heterocyclic 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 three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/14Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D417/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/14Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings

Abstract

Reivindicación 1: Un compuesto de fórmula (1) donde R¹ representa heteroaril-alquilo C₁₋₂, donde el heteroarilo es un anillo aromático monocíclico o bicíclico de 5 a 10 miembros que contiene 1, 2 ó 3 heteroátomos seleccionados independientemente entre oxígeno, nitrógeno y azufre, y donde el heteroarilo está sin sustituir o sustituido una o dos veces con alquilo C₁₋₄; o heterociclil-alquilo C₁₋₂ donde el heterociclilo es un anillo no aromático monocíclico de 5 ó 6 miembros que contiene uno o dos átomos de nitrógeno que está anillado a un anillo de fenilo o piridinilo, y donde el heterociclilo está sin sustituir o sustituido una o dos veces donde los sustituyentes son independientemente seleccionados del grupo que consiste en alquilo C₁₋₄ y oxo; R² representa hidrógeno o metilo; R³ representa arilo, donde el arilo es un grupo fenilo o naftilo, grupos los cuales están independientemente sin sustituir o sustituidos una o dos veces donde los sustituyentes son independientemente seleccionados del grupo que consiste en halógeno, alquilo C₁₋₄, alcoxi C₁₋₄, fluoroalquilo C₁₋₂, fluoroalcoxi C₁₋₂ y ciano; aril-alquilo C₁₋₂, donde el arilo es un grupo fenilo o naftilo, dichos grupos están independientemente no sustituidos o sustituidos una vez con halógeno; heteroarilo, donde el heteroarilo es un anillo aromático monocíclico o bicíclico de 5 a 10 miembros que contiene 1, 2 ó 3 heteroátomos seleccionados independientemente entre oxígeno, nitrógeno y azufre, y donde el heteroarilo está sin sustituir o sustituido una o dos veces donde los sustituyentes son independientemente seleccionados del grupo que consiste en halógeno, alquilo C₁₋₄, cicloalquilo C₃₋₆, alcoxi C₁₋₄, fluoroalquilo C₁₋₂, fluoroalcoxi C₁₋₂, di-alquil C₁₋₂-amino, hidroxi, ciano, fenilo, piridinilo y heteroaril-alquilo C₁₋₂, donde el heteroarilo es un anillo aromático monocíclico de 5 ó 6 miembros que contiene 1 ó 2 heteroátomos seleccionados independientemente entre oxígeno, nitrógeno y azufre; aril-alquil C₁₋₂-sulfonilo, donde el arilo es un grupo fenilo o naftilo; o R⁶-carbonilo; R⁴ representa hidrógeno, halógeno, fluoroalquilo C₁₋₂ o ciano; R⁵ representa hidrógeno, halógeno o fluoroalquilo C₁₋₂; y R⁶ representa alquilo C₁₋₄; cicloalquilo C₃₋₆, donde el cicloalquilo está sin sustituir o sustituido una vez con fenilo; cicloalquilo C₅₋₆, donde el cicloalquilo está anillado a un anillo de fenilo; alcoxi C₁₋₂-alquilo C₁₋₂; arilo, donde el arilo es un grupo fenilo o naftilo, grupos los cuales están independientemente sin sustituir o sustituidos una o dos veces donde los sustituyentes son independientemente seleccionados del grupo que consiste en halógeno, alquilo C₁₋₄, alcoxi C₁₋₄, fluoroalquilo C₁₋₂ y di-alquil C₁₋₂-amino; aril-alquilo C₁₋₂, donde el arilo es un grupo fenilo o naftilo, grupos los cuales están independientemente sin sustituir o sustituidos una o dos veces donde los sustituyentes son independientemente seleccionados del grupo que consiste en halógeno y alcoxi C₁₋₄; ariloxi-alquilo C₁₋₂, donde el arilo es un grupo fenilo o naftilo; aril-alcoxi C₁₋₂, donde el arilo es un grupo fenilo o naftilo; heterociclil-alquilo C₁₋₂, donde el heterociclilo es un anillo no aromático monocíclico de 5 ó 6 miembros que contiene uno o dos heteroátomos seleccionados independientemente entre oxígeno y nitrógeno; heteroarilo, donde el heteroarilo es un anillo aromático monocíclico o bicíclico de 5 a 10 miembros que contiene 1, 2 ó 3 heteroátomos seleccionados independientemente entre oxígeno, nitrógeno y azufre, y donde el heteroarilo está sin sustituir o sustituido una vez con alquilo C₁₋₄; o heteroaril-alquilo C₁₋₂, donde el heteroarilo es un anillo aromático monocíclico o bicíclico de 5 a 10 miembros que contiene 1, 2 ó 3 heteroátomos seleccionados independientemente entre oxígeno, nitrógeno y azufre; o su sal.
ARP150100819A 2014-03-24 2015-03-18 Derivados de 8-(piperazin-1-il)-1,2,3,4-tetrahidro-isoquinolina AR099789A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
IB2014060092 2014-03-24

Publications (1)

Publication Number Publication Date
AR099789A1 true AR099789A1 (es) 2016-08-17

Family

ID=52815062

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP150100819A AR099789A1 (es) 2014-03-24 2015-03-18 Derivados de 8-(piperazin-1-il)-1,2,3,4-tetrahidro-isoquinolina

Country Status (14)

Country Link
US (1) US9951063B2 (es)
EP (1) EP3122741B1 (es)
JP (1) JP6424234B2 (es)
KR (1) KR102356410B1 (es)
CN (1) CN106103426B (es)
AR (1) AR099789A1 (es)
AU (1) AU2015237826A1 (es)
BR (1) BR112016022046A8 (es)
CA (1) CA2939893C (es)
ES (1) ES2682398T3 (es)
MX (1) MX2016012451A (es)
RU (1) RU2016141443A (es)
TW (1) TW201623280A (es)
WO (1) WO2015145322A1 (es)

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU2014295123B2 (en) 2013-07-22 2018-08-02 Idorsia Pharmaceuticals Ltd 1-(piperazin-1-yl)-2-([1,2,4]triazol-1-yl)-ethanone derivatives
AR103399A1 (es) 2015-01-15 2017-05-10 Actelion Pharmaceuticals Ltd Derivados de (r)-2-metil-piperazina como moduladores del receptor cxcr3
CN107250133B (zh) * 2015-01-15 2020-09-15 爱杜西亚药品有限公司 作为cxcr3受体调节剂的羟烷基哌嗪衍生物
US11046670B2 (en) 2015-10-19 2021-06-29 Board Of Regents, The University Of Texas System Piperazinyl norbenzomorphan compounds and methods for using the same
WO2017190109A1 (en) * 2016-04-29 2017-11-02 Board Of Regents, The University Of Texas System Sigma receptor binders
WO2018011265A1 (en) 2016-07-13 2018-01-18 Idorsia Pharmaceuticals Ltd Hydroxyalkyl-piperazine derivatives as cxcr3 receptor modulators
WO2018083136A1 (en) * 2016-11-03 2018-05-11 F. Hoffmann-La Roche Ag Novel tetrahydroisoquinolines and terahydronaphthyridines for the treatment and prophylaxis of hepatitis b virus infection
CN108794456B (zh) * 2018-04-28 2020-07-14 北京施安泰医药技术开发有限公司 一类抗乙肝药物、其制备方法、药物组合物及其用途
CN115843298B (zh) 2020-07-22 2024-03-29 南京正大天晴制药有限公司 一种二氢吡啶并[2,3-d]嘧啶酮衍生物的盐及晶型
KR102281647B1 (ko) * 2020-12-09 2021-07-30 메디케어제약 주식회사 피페라진-퀴놀린 유도체의 제조방법

Family Cites Families (88)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE60031285T2 (de) * 1999-08-27 2007-08-30 Chemocentryx Inc., Mountain View Heterozyclische verbindungen und verfahren zur modulierung von cxcr3 funktion
CA2432985A1 (en) 2001-01-23 2002-08-01 Vincent Mancuso Piperazine- and piperidine-derivatives as melanocortin receptor agonists
EP1368339A1 (en) 2001-01-23 2003-12-10 Eli Lilly & Company Substituted piperidines/piperazines as melanocortin receptor agonists
EP1363631A4 (en) 2001-03-02 2005-11-16 Bristol Myers Squibb Co "COMPOUNDS SUITED AS MODULATORS OF MELANOCORTIN RECEPTORS AND THESE PHARMACEUTICAL COMPOSITIONS CONTAINING THEREOF"
US20050256130A1 (en) 2002-06-12 2005-11-17 Chemocentryx, Inc. Substituted piperazines
US7842693B2 (en) 2002-06-12 2010-11-30 Chemocentryx, Inc. Substituted piperazines
WO2003105853A1 (en) 2002-06-12 2003-12-24 Chemocentryx, Inc. 1-aryl-4-substituted piperazines derivatives for use as ccr1 antagonists for the treatment of inflammation and immune disorders
US7589199B2 (en) 2002-06-12 2009-09-15 Chemocentryx, Inc. Substituted piperazines
GB0315203D0 (en) 2003-06-28 2003-08-06 Celltech R&D Ltd Chemical compounds
WO2005035534A1 (ja) 2003-10-08 2005-04-21 Ono Pharmaceutical Co., Ltd. 複素ビシクロ環および複素トリシクロ環化合物およびその医薬
US20050124625A1 (en) 2003-10-21 2005-06-09 Salvati Mark E. Piperazine derivatives and their use as modulators of nuclear hormone receptor function
US20050119252A1 (en) 2003-10-22 2005-06-02 Neurocrine Biosciences, Inc. Ligands of melanocortin receptors and compositions and methods related thereto
GB0325956D0 (en) 2003-11-06 2003-12-10 Addex Pharmaceuticals Sa Novel compounds
CN1882347A (zh) 2003-11-21 2006-12-20 阿雷生物药品公司 Akt蛋白激酶抑制剂
US20060276465A1 (en) 2003-12-26 2006-12-07 Eisai R&D Management Co., Ltd. 1,2-di(cyclic) substituted benzene compounds
MY140489A (en) 2003-12-26 2009-12-31 Eisai R&D Man Co Ltd 1,2-di (cyclic) substituted benzene compounds
CN101189238A (zh) 2005-02-16 2008-05-28 先灵公司 具有cxcr3拮抗剂活性的哌嗪-哌啶
MX2007009948A (es) 2005-02-16 2007-09-26 Schering Corp Pierazin-piperidinas sustituidas con piridilo y fenilo conectados por aminos con actividad antagonista de cxcr3.
US7868005B2 (en) 2005-02-16 2011-01-11 Schering Corporation Pyrazinyl substituted piperazine-piperidines with CXCR3 antagonist activity
KR20070107075A (ko) 2005-02-16 2007-11-06 쉐링 코포레이션 Cxcr3 길항제 활성을 갖는 신규의 헤테로사이클릭치환된 피리딘 또는 페닐 화합물
CA2598456A1 (en) 2005-02-16 2006-08-24 Schering Corporation Heterocyclic substituted piperazines with cxcr3 antagonist activity
KR20070107040A (ko) 2005-02-16 2007-11-06 쉐링 코포레이션 Cxcr3 길항제 활성을 갖는 헤테로아릴-치환된피라지닐-피페라진-피페리딘
CN101213185A (zh) 2005-02-16 2008-07-02 先灵公司 具有cxcr3拮抗活性的吡啶基和苯基取代的哌嗪-哌啶
WO2007002742A1 (en) 2005-06-28 2007-01-04 Pharmacopeia, Inc. Substituted [1,4]-diazepanes as cxcr3 antagonists and their use in the treatment of inflammatory disorders
US7754724B2 (en) 2005-06-30 2010-07-13 Dow Agrosciences Llc N-substituted piperazines
TW200738701A (en) 2005-07-26 2007-10-16 Du Pont Fungicidal carboxamides
ES2382163T3 (es) 2005-10-11 2012-06-05 Schering Corporation Compuestos heterocíclicos sustituidos con actividad antagonista de CXCR3
EP1957076A2 (en) 2005-11-29 2008-08-20 Merck & Co., Inc. Thiazole derivatives as cxcr3 receptor modulators
WO2007070433A2 (en) 2005-12-12 2007-06-21 Merck & Co., Inc. 2-arylthiazole derivatives as cxcr3 receptor modulators
WO2007076318A2 (en) 2005-12-21 2007-07-05 Smithkline Beecham Corporation Camphor-derived cxcr3 antagonists
EP1988900A2 (en) * 2006-02-23 2008-11-12 Merck & Co., Inc. Pyridine, pyrimidine and pyrazine derivatives as cxcr3 receptor modulators
WO2007109238A1 (en) 2006-03-21 2007-09-27 Schering Corporation Heterocyclic substituted pyridine compounds with cxcr3 antagonist activity
FR2903405B1 (fr) 2006-07-04 2011-09-09 Pasteur Institut Composes a effet potentialisateur de l'activite de l'ethionamide et leurs applications
KR20090043512A (ko) 2006-07-14 2009-05-06 쉐링 코포레이션 Cxcr3 길항제 활성을 갖는 헤테로사이클릭 치환된 피페라진 화합물
WO2008013622A2 (en) 2006-07-27 2008-01-31 E. I. Du Pont De Nemours And Company Fungicidal azocyclic amides
JP2010513520A (ja) 2006-12-22 2010-04-30 シェーリング コーポレイション Cxcr3アンタゴニスト活性を有する複素環式化合物
WO2008091594A2 (en) 2007-01-24 2008-07-31 E. I. Du Pont De Nemours And Company Fungicidal mixtures
JP5337711B2 (ja) 2007-01-25 2013-11-06 イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー 殺菌性アミド
EP2185154A2 (en) 2007-08-03 2010-05-19 Schering Corporation Method of treating cxcr3 mediated diseases using heterocyclic substituted piperazines
TWI428091B (zh) 2007-10-23 2014-03-01 Du Pont 殺真菌劑混合物
WO2009079490A1 (en) 2007-12-18 2009-06-25 Schering Corporation Process and intermediates for the synthesis of heterocyclic substituted piperazines with cxcr3 antagonist activity
KR20150065958A (ko) 2008-01-25 2015-06-15 이 아이 듀폰 디 네모아 앤드 캄파니 살균제 복소환 화합물
KR20100105890A (ko) 2008-01-25 2010-09-30 이 아이 듀폰 디 네모아 앤드 캄파니 살균제 아미드
PE20091576A1 (es) 2008-02-19 2009-11-05 Sanofi Aventis DERIVADOS DE 3-(AMIDO O SULFAMIDO)-4-(4-AZINIL SUSTITUIDO)BENZAMIDA COMO INHIBIDORES DEL RECEPTOR DE QUIMIOQUINAS CxCR3
KR20100135952A (ko) 2008-04-30 2010-12-27 바이엘 크롭사이언스 아게 식물 보호제로서의 티아졸-4-카복실산 에스테르 및 티오에스테르
JP5785495B2 (ja) 2008-10-01 2015-09-30 バイエル・インテレクチュアル・プロパティ・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツングBayer Intellectual Property GmbH 植物保護剤としてのヘテロシクリル置換チアゾール類
KR101052065B1 (ko) 2008-10-15 2011-07-27 한국과학기술연구원 칼슘이온 채널 조절제로서 유효한 피라졸릴메틸아민-피페라진 유도체와 이의 제조방법
TW201036966A (en) 2008-12-02 2010-10-16 Du Pont Fungicidal heterocyclic compounds
JP2012511525A (ja) 2008-12-11 2012-05-24 バイエル・クロップサイエンス・アーゲー 植物保護剤としてのチアゾリルオキシムエーテルおよびヒドラゾン
US8362249B2 (en) 2009-04-27 2013-01-29 Boehringer Ingelheim International Gmbh CXCR3 receptor antagonists
WO2010126811A1 (en) * 2009-04-27 2010-11-04 Boehringer Ingelheim International Gmbh Cxcr3 receptor antagonists
EP2272846A1 (de) 2009-06-23 2011-01-12 Bayer CropScience AG Thiazolylpiperidin Derivate als Fungizide
AU2010283832A1 (en) 2009-08-12 2012-02-23 Syngenta Participations Ag Microbiocidal heterocycles
UA107938C2 (en) 2009-08-12 2015-03-10 Syngenta Participations Ag Heterocycles with microbicidal properties
WO2011051243A1 (en) 2009-10-29 2011-05-05 Bayer Cropscience Ag Active compound combinations
JP5827626B2 (ja) 2009-10-30 2015-12-02 バイエル・インテレクチュアル・プロパティ・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツングBayer Intellectual Property GmbH ヘテロアリールピペリジン及びピペラジン誘導体
CN102781937B (zh) 2009-12-21 2015-09-30 拜尔农作物科学股份公司 用作杀菌剂的双(二氟甲基)吡唑
US8952004B2 (en) 2010-01-07 2015-02-10 Boehringer Ingelheim International Gmbh CXCR3 receptor antagonists
ES2613066T3 (es) 2010-04-28 2017-05-22 Bayer Intellectual Property Gmbh Derivados de cetoheteroarilpiperidina y -piperazina como fungicidas
US8815775B2 (en) 2010-05-18 2014-08-26 Bayer Cropscience Ag Bis(difluoromethyl)pyrazoles as fungicides
EP2571866A1 (en) 2010-05-20 2013-03-27 E.I. Du Pont De Nemours And Company Fungicidal oximes and hydrazones
BR112012030184A2 (pt) 2010-05-27 2015-12-29 Bayer Cropscience Ag derivados de ácido piridinilcarboxílico como fungicidas
US20120122928A1 (en) 2010-08-11 2012-05-17 Bayer Cropscience Ag Heteroarylpiperidine and -Piperazine Derivatives as Fungicides
US8759527B2 (en) 2010-08-25 2014-06-24 Bayer Cropscience Ag Heteroarylpiperidine and -piperazine derivatives as fungicides
KR101797074B1 (ko) 2010-10-27 2017-11-13 바이엘 인텔렉쳐 프로퍼티 게엠베하 살진균제로서의 헤테로아릴 피페리딘 및 헤테로아릴 피페라진 유도체
EP2643312B1 (en) 2010-11-25 2014-09-10 Syngenta Participations AG Microbicidal heterocycles
MX2013006936A (es) 2010-12-17 2013-07-22 Du Pont Ambas azociclicas fungicidas.
KR101848116B1 (ko) 2011-02-01 2018-04-11 바이엘 인텔렉쳐 프로퍼티 게엠베하 살진균제로서의 헤테로아릴 피페리딘 및 헤테로아릴 피페라진 유도체
WO2012107475A1 (en) 2011-02-10 2012-08-16 Syngenta Participations Ag Microbiocidal pyrazole derivatives
AR085333A1 (es) 2011-02-10 2013-09-25 Syngenta Participations Ag Derivados de pirazol microbicidas
CN102827073A (zh) 2011-06-17 2012-12-19 安吉奥斯医药品有限公司 治疗活性组合物和它们的使用方法
WO2013037768A1 (de) 2011-09-15 2013-03-21 Bayer Intellectual Property Gmbh Piperidinpyrazole als fungizide
WO2013056915A1 (en) 2011-10-18 2013-04-25 Syngenta Participations Ag Microbiocidal pyrazole derivatives
WO2013056911A1 (en) 2011-10-18 2013-04-25 Syngenta Participations Ag Microbiocidal pyrazole derivatives
US8642774B2 (en) 2011-12-08 2014-02-04 Boehringer Ingelheim International Gmbh Compounds
EP2794563B1 (en) 2011-12-21 2017-02-22 Actelion Pharmaceuticals Ltd Heterocyclyl derivatives and their use as prostaglandin d2 receptor modulators
US8889677B2 (en) 2012-01-17 2014-11-18 Boehringer Ingellheim International GmbH Substituted triazoles useful as mGlu5 receptor modulators
BR112014018714A8 (pt) 2012-02-02 2017-12-26 Actelion Pharmaceuticals Ltd Compostos de 4-(benzoimidazol-2-il)-tiazol e derivados de aza relacionados
DE102012203270A1 (de) 2012-03-01 2013-09-05 Bundesdruckerei Gmbh Dokument und Verfahren zum Herstellen des Dokuments
EP2820015A1 (en) 2012-03-02 2015-01-07 Syngenta Participations AG Microbiocidal pyrazole derivatives
WO2014062938A1 (en) 2012-10-19 2014-04-24 Bristol-Myers Squibb Company Rory modulators
WO2014075873A1 (en) 2012-11-13 2014-05-22 Syngenta Participations Ag Microbiocidal pyrazole derivatives
WO2014075874A1 (en) 2012-11-13 2014-05-22 Syngenta Participations Ag Microbiocidal pyrazole derivatives
ES2695350T3 (es) 2012-12-11 2019-01-03 Takeda Pharmaceuticals Co Compuesto heterocíclico
TWI632142B (zh) 2013-06-24 2018-08-11 德商拜耳作物科學股份有限公司 作為殺真菌劑之六氫吡啶羧酸衍生物
AU2014295123B2 (en) 2013-07-22 2018-08-02 Idorsia Pharmaceuticals Ltd 1-(piperazin-1-yl)-2-([1,2,4]triazol-1-yl)-ethanone derivatives
CN107250133B (zh) 2015-01-15 2020-09-15 爱杜西亚药品有限公司 作为cxcr3受体调节剂的羟烷基哌嗪衍生物
AR103399A1 (es) 2015-01-15 2017-05-10 Actelion Pharmaceuticals Ltd Derivados de (r)-2-metil-piperazina como moduladores del receptor cxcr3

Also Published As

Publication number Publication date
TW201623280A (zh) 2016-07-01
JP2017508773A (ja) 2017-03-30
ES2682398T3 (es) 2018-09-20
CA2939893C (en) 2022-07-19
WO2015145322A1 (en) 2015-10-01
JP6424234B2 (ja) 2018-11-14
CA2939893A1 (en) 2015-10-01
KR102356410B1 (ko) 2022-01-26
EP3122741B1 (en) 2018-06-06
BR112016022046A8 (pt) 2017-12-26
RU2016141443A (ru) 2018-04-25
CN106103426B (zh) 2019-03-19
US9951063B2 (en) 2018-04-24
US20170107214A1 (en) 2017-04-20
CN106103426A (zh) 2016-11-09
KR20160135798A (ko) 2016-11-28
EP3122741A1 (en) 2017-02-01
MX2016012451A (es) 2017-01-06
AU2015237826A1 (en) 2016-11-03
BR112016022046A2 (pt) 2017-08-15

Similar Documents

Publication Publication Date Title
AR099789A1 (es) Derivados de 8-(piperazin-1-il)-1,2,3,4-tetrahidro-isoquinolina
AR110405A1 (es) Compuestos
AR100645A1 (es) Derivados de pirazolo-pirimidina
AR106605A1 (es) Oxadiazoles sustituidos para combatir hongos fitopatógenos
AR104884A1 (es) Compuestos de 4-hidroxi-3-(heteroaril)piridin-2-ona como agonistas de apj
AR099995A1 (es) Piridilamidinas fungicidas
AR102177A1 (es) Compuestos de heteroarilo como inhibidores de btk y usos de los mismos
AR094299A1 (es) Derivados de ftalazin-1(2h)-ona sustituidos
AR093921A1 (es) Derivados de indol carboxamida como antagonistas del receptor p2x7
AR095311A1 (es) 3-pirimidin-4-il-oxazolidin-2-onas como inhibidores de idh mutante
AR097279A1 (es) Derivados de benzimidazolil-metil urea como agonistas del receptor de alx
AR104025A1 (es) Carbamatos de piperazina como moduladores de magl y/o abhd6, procesos para su preparación y composiciones farmacéuticas
AR094812A1 (es) Derivado de piridina monocíclico como inhibidor del fgfr
AR100809A1 (es) Inhibidores de fosfatidilinositol 3-quinasa
AR100712A1 (es) Compuestos de pirazol como bloqueadores de los canales de calcio tipo t
AR096979A1 (es) Derivados de pirrol, su procedimiento de preparación y las composiciones farmacéuticas que los contienen
AR091519A1 (es) Inhibidores pirrolopirazona de tanquirasa
AR095359A1 (es) Compuestos heteroaromáticos y su uso como ligandos d1 de dopamina
AR103414A1 (es) Derivados de hidroxialquil-piperazina como moduladores del receptor cxcr3
AR102079A1 (es) DERIVADOS BICÍCLICOS QUE TIENEN ACTIVIDAD COMO AGONISTAS ADRENÉRGICOS b2 Y COMO ANTAGONISTAS MUSCARÍNICOS M3
AR103742A1 (es) Derivados de trifluorometilpropanamida
AR109296A1 (es) Derivados de oxadiazolopiridina para el uso como inhibidores de ghrelin o-aciltransferasa (goat)
AR109711A1 (es) Inhibidores de fosfatidilinositol 3-quinasa
AR100439A1 (es) Derivados de carboxamida
AR097252A1 (es) Derivado de pirazolilpirazol sustituido y el uso del mismo como herbicida

Legal Events

Date Code Title Description
FB Suspension of granting procedure