HUP0002853A2 - 6,7-Helyzetben aszimmetrikusan diszubsztituált kinoxalinkarbonsav-származékok, és ezeket a vegyületeket tartalmazó gyógyszerkészítmények - Google Patents

6,7-Helyzetben aszimmetrikusan diszubsztituált kinoxalinkarbonsav-származékok, és ezeket a vegyületeket tartalmazó gyógyszerkészítmények

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Publication number
HUP0002853A2
HUP0002853A2 HU0002853A HUP0002853A HUP0002853A2 HU P0002853 A2 HUP0002853 A2 HU P0002853A2 HU 0002853 A HU0002853 A HU 0002853A HU P0002853 A HUP0002853 A HU P0002853A HU P0002853 A2 HUP0002853 A2 HU P0002853A2
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Hungary
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group
general formula
optionally
optionally substituted
atom
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HU0002853A
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English (en)
Inventor
Naoki Ando
Tsuyoshi Anraku
Jun Asano
Kazunori Fukuchi
Futoshi Shiga
Masanori Takadoi
Yasuo Takano
Hideharu Uchiki
Junichiro Uda
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Kyorin Pharmaceutical Co. Ltd.
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Publication of HUP0002853A2 publication Critical patent/HUP0002853A2/hu
Publication of HUP0002853A3 publication Critical patent/HUP0002853A3/hu

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    • C07D231/02Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
    • C07D231/10Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D231/12Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three 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
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    • C07D241/38Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings condensed with carbocyclic rings or ring systems with only hydrogen or carbon atoms directly attached to the ring nitrogen atoms
    • C07D241/40Benzopyrazines
    • C07D241/44Benzopyrazines 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 carbon atoms of the hetero ring
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    • C07D207/04Heterocyclic 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
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    • C07D207/33Heterocyclic 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 ring carbon atoms
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    • C07D209/44Iso-indoles; Hydrogenated iso-indoles
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    • C07D213/60Heterocyclic 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 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
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    • C07D233/56Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms
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    • C07D233/66Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two 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
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    • C07D295/12Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly or doubly bound nitrogen atoms
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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Coloring (AREA)
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Abstract

A találmány szerinti vegyületek (1) általános képletében Q jelentésehalogénatom, adott esetben halogénatommal szubsztituált alkilcsoport,(2) általános képletű csoport, ahol Ar jelentése adott esetbenszubsztituált fenilcsoport vagy naftilcsoport, P jelentésealkiléncsoport, alkeniléncsoport, alkiniléncsoport, oxigénatom vagykénatom, vagy (3) általános képletű aril- vagy heteroarilcsoportottartalmazó csoport, R jelentése nitrocsoport, trifluormetilcsoport,adott esetben szubsztituált aminocsoport vagy (7) általános képletűcsoport, R1 jelentése aralkilcsoport, fenilcsoport, naftilcsoport, 5-vagy 6-tagú heterociklusos csoport és ennek kondenzált gyűrűi, amelyekaz aromás gyűrűn vagy heterociklusos gyűrűn adott esetben egy vagytöbb szubsztituenssel szubsztituálva lehetnek, hidrogénatom, adottesetben szubsztituált alkilcsoport, vagy cikloalkilcsoport, R2jelentése hidroxilcsoport, alkoxicsoport vagy (6) általános képletűcsoport. A találmány kiterjed a fenti vegyületeket tartalmazógyógyszerkészítményekre, amelyek felhasználhatók a cerebrálisidegsejtek rendellenességeinek kezelésére. Ó
HU0002853A 1997-09-01 1998-08-28 6,7-asymmetrically disubstituted quinoxalinecarboxylic acid derivatives, and pharmaceutical compositions containing them HUP0002853A3 (en)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
JP25131397 1997-09-01
JP19010998 1998-07-06
JP19010898 1998-07-06
PCT/JP1998/003832 WO1999011632A1 (fr) 1997-09-01 1998-08-28 Derives d'acide quinoxalinecarboxylique disubstitues en position 6,7-asymetrique, sels d'addition de ces derives, et procedes de preparation de ces derives et de ces sels

Publications (2)

Publication Number Publication Date
HUP0002853A2 true HUP0002853A2 (hu) 2001-05-28
HUP0002853A3 HUP0002853A3 (en) 2001-12-28

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HU0002853A HUP0002853A3 (en) 1997-09-01 1998-08-28 6,7-asymmetrically disubstituted quinoxalinecarboxylic acid derivatives, and pharmaceutical compositions containing them

Country Status (13)

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US (1) US6348461B1 (hu)
EP (1) EP1020453B1 (hu)
KR (1) KR100588247B1 (hu)
CN (1) CN1161344C (hu)
AT (1) ATE267176T1 (hu)
AU (1) AU744540B2 (hu)
BR (1) BR9811739A (hu)
CA (1) CA2302161A1 (hu)
DE (1) DE69824025T2 (hu)
HU (1) HUP0002853A3 (hu)
NO (1) NO315272B1 (hu)
NZ (1) NZ503076A (hu)
WO (1) WO1999011632A1 (hu)

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JP2000309585A (ja) * 1999-02-26 2000-11-07 Kyorin Pharmaceut Co Ltd 6−置換ヘテロキノリンカルボン酸誘導体とその付加塩及びそれらの製造方法
JP2000309586A (ja) * 1999-02-26 2000-11-07 Kyorin Pharmaceut Co Ltd 6−置換−7−ヘテロキノキサリンカルボン酸誘導体とその付加塩及びそれらの製造方法
EP1601665A2 (en) * 2003-03-07 2005-12-07 Glaxo Group Limited Urea derivatives
WO2005056547A2 (en) * 2003-12-04 2005-06-23 Vertex Pharmaceuticals Incorporated Quinoxalines useful as inhibitors of protein kinases
CA2690485A1 (en) * 2007-06-11 2008-12-18 Valletta Health Ip Ee B.V. Urocanic acid derivatives useful for the treatment of immune-related and inflammatory diseases
CA2694882C (en) * 2007-08-01 2015-05-12 Kumiai Chemical Industry Co., Ltd. Oxopyrazine derivative and herbicide
EA021904B1 (ru) * 2008-03-05 2015-09-30 Мерк Патент Гмбх Производные хиноксалинона в качестве стимуляторов секреции инсулина, способы их получения и их применение для лечения диабета
EP2537844A1 (en) 2008-07-21 2012-12-26 Purdue Pharma L.P. Substituted-quinoxaline-type bridged-piperidine compounds and the uses thereof
EP2261211A1 (en) * 2009-05-20 2010-12-15 Université de Lille 2 Droit et Santé 1,4-dihydropyridine derivatives and their uses
US8859803B2 (en) 2009-06-26 2014-10-14 Ihara Chemical Industry Co., Ltd. Process for production of ketomalonic acid compounds or hydrates thereof
KR101117129B1 (ko) * 2009-09-14 2012-02-24 한국화학연구원 신규한 퀴녹살린 유도체 및 이를 포함하는 줄기세포의 신경세포로의 분화유도용 조성물
CN107245056A (zh) 2011-08-26 2017-10-13 润新生物公司 化学实体、组合物及方法
CN115403531A (zh) 2011-09-14 2022-11-29 润新生物公司 作为激酶抑制剂的化学实体、组合物及方法
EP2757885B1 (en) 2011-09-21 2017-03-15 Neupharma, Inc. Certain chemical entites, compositions, and methods
WO2013049701A1 (en) 2011-09-30 2013-04-04 Neupharma, Inc. Certain chemical entities, compositions, and methods
EP2806874B1 (en) 2012-01-25 2017-11-15 Neupharma, Inc. Quinoxaline-oxy-phenyl derivatives as kinase inhibitors
US9688635B2 (en) 2012-09-24 2017-06-27 Neupharma, Inc. Certain chemical entities, compositions, and methods
EP2916838B1 (en) 2012-11-12 2019-03-13 Neupharma, Inc. Certain chemical entities, compositions, and methods
JP5921500B2 (ja) 2013-07-19 2016-05-24 イハラケミカル工業株式会社 ケトマロン酸化合物の製造方法
KR102134407B1 (ko) 2014-02-17 2020-07-15 구미아이 가가쿠 고교 가부시키가이샤 유통 반응기를 사용한 케토말론산 화합물의 연속 제조방법
CN108570038B (zh) * 2017-03-08 2021-09-28 中国科学院上海药物研究所 二氢喹喔啉类溴结构域识别蛋白抑制剂及制备方法和用途

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KR100588247B1 (ko) 2006-06-13
KR20010023535A (ko) 2001-03-26
AU8886498A (en) 1999-03-22
BR9811739A (pt) 2000-09-19
HUP0002853A3 (en) 2001-12-28
NO20001046D0 (no) 2000-03-01
ATE267176T1 (de) 2004-06-15
NZ503076A (en) 2002-10-25
CN1269794A (zh) 2000-10-11
CN1161344C (zh) 2004-08-11
CA2302161A1 (en) 1999-03-11
WO1999011632A1 (fr) 1999-03-11
EP1020453B1 (en) 2004-05-19
EP1020453A1 (en) 2000-07-19
US6348461B1 (en) 2002-02-19
DE69824025T2 (de) 2005-06-16
NO20001046L (no) 2000-05-02
AU744540B2 (en) 2002-02-28
EP1020453A4 (en) 2000-11-08
NO315272B1 (no) 2003-08-11
DE69824025D1 (de) 2004-06-24

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