HUP0101688A2 - Heterociklussal szubsztituált amidok és alkalmazásuk gyógyszerkészítmények előállítására - Google Patents

Heterociklussal szubsztituált amidok és alkalmazásuk gyógyszerkészítmények előállítására

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HUP0101688A2
HUP0101688A2 HU0101688A HUP0101688A HUP0101688A2 HU P0101688 A2 HUP0101688 A2 HU P0101688A2 HU 0101688 A HU0101688 A HU 0101688A HU P0101688 A HUP0101688 A HU P0101688A HU P0101688 A2 HUP0101688 A2 HU P0101688A2
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nhco
optionally
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Monika Knopp
Wilfried Lubisch
Achim Möller
Hans-Jörg Treiber
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Basf Ag
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  • Organic Chemistry (AREA)
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  • Urology & Nephrology (AREA)
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  • Orthopedic Medicine & Surgery (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Vascular Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Pyridine Compounds (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
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Abstract

A találmány tárgyát az általános képletű amidok - ahol R1 adottesetben szubsztituált, adott esetben gyűrűtag heteroatomot tartalmazóaromás csoport, R2 halogénatom, alkil-, alkenil-, alkinil-, alkil-fenil-, alkenil-fenil-csoport, alkinil-fenil-csoport, fenil-, NHCO-alkil-, NHSO2-alkil-, NHCO-fenil-, nitro-, alkoxi- és aminocsoport,ahol az aromás gyűrűk maguk is további egy-két szubsztituensthordozhatnak, és két R2 csoport együtt - CH=CH-CH=CH-láncot isjelenthet, azaz a két R2 csoport együtt adott esetben szubsztituáltanellált benzogyűrűt is képezhet, R3 alkilcsoport, amelyet adottesetben metil-tio-, fenil-, ciklohexil-, cikloheptil-, ciklopentil-,indolil-, piridil- vagy naftilcsoport szubsztituálhat, ahol a gyűrűscsoportok maguk is szubsztituáltak lehetnek, X-(CH2)m-, -(CH2)m-O-(-(CH2)o-, -(CH2)o-S-(CH2)m-, -(CH2)o-SO-(CH2)m-, -(CH2)o-SO2-(CH2)m-,etenilén-, etinilén-, -CO-CH=CH-, -(CH2)o-CO-(CH2)m-, -(CH2)m-NHCO-(CH2)o-, -(CH2)m-CONH-(CH2)o-, -(CH2)m-NHSO2-(CH2)o-, -NH-CO-CH=CH-, -(CH2)m-SO2NH-(CH2)o-, -CONH-csoport, és általános képletű csoport, R1és X együtt (általános) képletű vegyületet is jelenthet, Y telítetlenheterociklusos csoport, és R4 hidrogénatom, -COOR6 és -CO-Z általánosképletű csoport, ahol Z jelentése mono- vagy dialkil-amino-csoport, és5- vagy 6-tagú, egy vagy két gyűrűtag aminocsoportot tartalmazó gyűrűscsoport, n értéke 0, 1 vagy 2, és m, o értéke egymástól függetlenül 0,1, 2, 3 vagy 4 -és tautomer és izomer formáik, lehetséges enantiomervagy diasztereomer formáik, valamint fiziológiailag elfogadható sóik,előállításuk és kalpaint-inhibitorként történő alkalmazásuk képezik. Ó
HU0101688A 1998-04-20 1999-04-19 Heterocyclically substituted amides and their use for producing pharmaceutical compositions HUP0101688A3 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE19817459A DE19817459A1 (de) 1998-04-20 1998-04-20 Neue heterozyklische substituierte Amide, Herstellung und Anwendung
PCT/EP1999/002611 WO1999054304A1 (de) 1998-04-20 1999-04-19 Heterozyklische substituierte amide, deren herstellung und anwendung

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HUP0101688A2 true HUP0101688A2 (hu) 2001-11-28
HUP0101688A3 HUP0101688A3 (en) 2002-12-28

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US (2) US6630493B1 (hu)
EP (1) EP1073638B1 (hu)
JP (1) JP4621350B2 (hu)
KR (1) KR20010042841A (hu)
CN (1) CN1301255A (hu)
AT (1) ATE402149T1 (hu)
AU (1) AU3927199A (hu)
BG (1) BG104831A (hu)
BR (1) BR9909772A (hu)
CA (1) CA2328438C (hu)
DE (2) DE19817459A1 (hu)
ES (1) ES2310937T3 (hu)
HR (1) HRP20000786A2 (hu)
HU (1) HUP0101688A3 (hu)
ID (1) ID26980A (hu)
IL (1) IL138704A0 (hu)
NO (1) NO20005264D0 (hu)
PL (1) PL343467A1 (hu)
SK (1) SK14522000A3 (hu)
TR (1) TR200003056T2 (hu)
WO (1) WO1999054304A1 (hu)
ZA (1) ZA200006718B (hu)

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IL138402A0 (en) * 1998-04-20 2001-10-31 Basf Ag Heterocyclically substituted amides used as calpain inhibitors
CN1303372A (zh) * 1998-05-25 2001-07-11 Basf公司 新的杂环取代酰胺、其制备以及应用
ATE312820T1 (de) * 1999-10-28 2005-12-15 Trine Pharmaceuticals Inc Pumpeninhibitoren zur freisetzung von medikamenten
DE10114762A1 (de) * 2001-03-26 2002-10-02 Knoll Gmbh Verwendung von Cysteinprotease-Inhibitoren
US7056917B2 (en) 2001-04-26 2006-06-06 Daiichi Pharmaceutical Co., Ltd. Drug efflux pump inhibitor
CA2445697A1 (en) * 2001-04-26 2002-11-07 Daiichi Pharmaceutical Co., Ltd. Drug efflux pump inhibitor
AR036375A1 (es) 2001-08-30 2004-09-01 Novartis Ag Compuestos pirrolo [2,3-d] pirimidina -2- carbonitrilo, un proceso para su preparacion, una composicion farmaceutica y el uso de dichos compuestos para la preparacion de medicamentos
KR100836547B1 (ko) 2002-01-11 2008-06-10 상꾜 가부시키가이샤 아미노 알코올 유도체 또는 포스폰산 유도체 및 이들을함유하는 의약 조성물
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NO20005264L (no) 2000-10-19
WO1999054304A1 (de) 1999-10-28
EP1073638A1 (de) 2001-02-07
ATE402149T1 (de) 2008-08-15
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ID26980A (id) 2001-02-22
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