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YU48854B - Derivati n-(4-piperidinil) (dihidrobenzofuran ili dihidro-2h-benzopiran)karboksamida i postupak za njihovo dobijanje - Google Patents

Derivati n-(4-piperidinil) (dihidrobenzofuran ili dihidro-2h-benzopiran)karboksamida i postupak za njihovo dobijanje

Info

Publication number
YU48854B
YU48854B YU39691A YU39691A YU48854B YU 48854 B YU48854 B YU 48854B YU 39691 A YU39691 A YU 39691A YU 39691 A YU39691 A YU 39691A YU 48854 B YU48854 B YU 48854B
Authority
YU
Yugoslavia
Prior art keywords
aryl
6alkyl
hydrogen
alkyl
het
Prior art date
Application number
YU39691A
Other languages
English (en)
Other versions
YU39691A (sh
Inventor
Georges Henri Paul Van Daele
Jean-Paul René Marie Andre Bosmans
Michel Anna Jozef De Cleyn
Original Assignee
Janssen Pharmaceutica N.V.
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 Janssen Pharmaceutica N.V. filed Critical Janssen Pharmaceutica N.V.
Priority to SI9110396A priority Critical patent/SI9110396B/sl
Priority to HR930483A priority patent/HRP930483B1/xx
Publication of YU39691A publication Critical patent/YU39691A/sh
Publication of YU48854B publication Critical patent/YU48854B/sh

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/12Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
    • 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
    • A61P1/04Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
    • 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
    • A61P1/10Laxatives
    • 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
    • A61P1/12Antidiarrhoeals
    • 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
    • A61P1/14Prodigestives, e.g. acids, enzymes, appetite stimulants, antidyspeptics, tonics, antiflatulents
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/14Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D513/00Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
    • C07D513/02Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
    • C07D513/04Ortho-condensed systems

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Engineering & Computer Science (AREA)
  • Veterinary Medicine (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Nutrition Science (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Cosmetics (AREA)
  • Pyrane Compounds (AREA)

Abstract

Jedinjenje formule njegov N-oksidni oblik, njegova so ili njegov stereohemijski izomerni oblik, u kojem: A je radikal formule -CH2- CH2- (a-1), - CH2- CH2- CH2- (a-2), ili - CH2-CH2-CH2-CH2- (a-3), u kojem jedan ili dva atoma vodonika u nevedenim radikalima (a-1) do (a-3) mogu biti zamenjeni sa C1-6alkil radikalom; R1 je vodonik ili halo; R2 je vodonik, amino, mono ili di(C1-6alkil)amino ili C1-6alkilkarbonilamino; R3 je vodonik ili C1-6alkil; L je C3-6cikloalkil, C5-6cikloalkanon, C3-6alkenil, u datom primeru supstituisan sa arilom, ili L je radikal formule -Alk-R4- (b-1), -Alk-X-R5- (b-2), -Alk-Y-C(=O)-R7 (b-3), ili -Alk-Y-C(=O)-NR9R10 (b-4), u kojoj svaki Alk je C1-6alkandiil; i R4 je vodonik, cijano, C1-6alkilsulfonilamino, C3-6cikloalkil, C5-6cikloalkanon, aril, di(aril)metil ili Het; R5 je vodonik, C1-6alkil, hidroksiC1-6alkil, C1-6cikloalkil, aril ili Het; X je O, S, SO2 ili NR6; navedeni R6 je vodonik, C1-6alkil ili aril; R7 je vodonik, C1-6alkil, C3-6cikloalkil, aril, arilC1-6alkil, di(aril)metil, C1-6alkiloksi ili hidroksi;Y je NR8 ili direktna veza; navedeni R8 je vodonik, C1-6alkil ili aril;R9 i R10 su svaki nezavisno vodonik, C1-6alkil, C3-6cikloalkil, aril ili arilC1-6alkil, ili R9 i R10 povezani sa atomom azota koji nosi R9 ili R10, mogu da obrazuju pirolidinil ili piperidinil prsten, pri cemu su oba u datom primeru supstituisana sa C1-6alkilom, aminom ili mono ili di(C1-6alkil)-aminom, ili navedeni R9 i R10 povezani sa azotom, koji nosi R9 i R10, mogu da obrazuju piperazinil ili 4-morfolinil radikal, pri cemu su oba u datom primeru supstituisana sa C1-6alkilom;svaki aril je nesupstituisani fenil ili fenil supstituisan sa 1, 2 ili 3 supstituenta, svaki nezavisno odabran iz grupe koju cine halo, hidroksi, C1-6alkil, C1-6alkoksi, aminosulfonil, C1-6alkilkarbonil, nitro, trifluorometil, amino ili aminokarbonil; a svaki Het je peto- ili sestoclani heterociklicni prsten, koji sadrzi 1, 2, 3 ili 4 hetero atoma odabrana izmedu kiseonika, sumpora ili azota, pod uslovom da nisu prisutna vise od 2 atoma kiseonika i/ili sumpora, pri cemu je navedeni peto- ili sestoclani prsten u datom primeru kondenzovan sa peto- ili sestoclanim, karboksilnim ili heterociklicnim prstenom, koji takode sdarzi 1, 2, 3 ili 4 hetero atoma odabrana izmedu kiseonika, sumpora i azota, pod uslovom, da ovaj poslednji prsten ne sadrzi vise od 2 atoma kiseonika i/ili sumpora i da je ukupan broj hetero atoma u sistemu biciklicnog prstena manji od 6; kada je Het moniociklican prstenasti sistem, u datom primeru moze biti supstituisan sa do 4 supstituenta; kada Het jeste biciklican prstenasti sistem, on moze u datom primeru biti supstituisan sa do 6 supstituenata; navedeni supstituenti su odabrani iz grupe koju cine halo, hidroksi, cijano, trifluorometil, C1-6alkil, aril C1-6alkil, aril, C1-6alkiloksi, C1-6alkiloksi C1-6alkil, hidroksi C1-6alkil, C1-6alkiltio, merkapto, nitro, amino mono i di(C1-6alkil)amino, aril C1-6alkilamino, aminokarbonil, mono i di(C1-6alkil)aminokarbo
YU39691A 1990-03-06 1991-03-06 Derivati n-(4-piperidinil) (dihidrobenzofuran ili dihidro-2h-benzopiran)karboksamida i postupak za njihovo dobijanje YU48854B (sh)

Priority Applications (2)

Application Number Priority Date Filing Date Title
SI9110396A SI9110396B (sl) 1990-03-06 1991-03-06 Derivati N-(4-piperidinil)(dihidrobenzofuran ali dihidro-2H-benzopiran) karboksamida
HR930483A HRP930483B1 (en) 1990-03-06 1993-03-23 N-(4-piperidinyl) (dihydrobenzofuran or dihydro-2h-benzopyran)carboxamide derivatives

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB909005014A GB9005014D0 (en) 1990-03-06 1990-03-06 N.(4.piperidinyl)(dihydrobenzofuran or dihydro.2h.benzopyran)carboxamide derivatives

Publications (2)

Publication Number Publication Date
YU39691A YU39691A (sh) 1994-06-10
YU48854B true YU48854B (sh) 2002-06-19

Family

ID=10672103

Family Applications (1)

Application Number Title Priority Date Filing Date
YU39691A YU48854B (sh) 1990-03-06 1991-03-06 Derivati n-(4-piperidinil) (dihidrobenzofuran ili dihidro-2h-benzopiran)karboksamida i postupak za njihovo dobijanje

Country Status (38)

Country Link
US (2) US5185335A (sh)
EP (1) EP0445862B1 (sh)
JP (1) JP2601566B2 (sh)
KR (1) KR0177521B1 (sh)
CN (1) CN1038936C (sh)
AT (1) ATE191912T1 (sh)
AU (1) AU636012B2 (sh)
BG (1) BG60381B1 (sh)
CA (1) CA2037575C (sh)
CY (1) CY2235B1 (sh)
CZ (1) CZ286617B6 (sh)
DE (1) DE69132119T2 (sh)
DK (1) DK0445862T3 (sh)
ES (1) ES2147175T3 (sh)
FI (1) FI101622B1 (sh)
GB (1) GB9005014D0 (sh)
GR (1) GR3033461T3 (sh)
HR (1) HRP930483B1 (sh)
HU (2) HU221627B1 (sh)
IE (1) IE910710A1 (sh)
IL (1) IL97018A (sh)
LT (1) LT3708B (sh)
LV (1) LV10085B (sh)
MA (1) MA22076A1 (sh)
MY (1) MY108831A (sh)
NO (1) NO177424C (sh)
NZ (1) NZ237189A (sh)
PL (6) PL168384B1 (sh)
PT (1) PT96937B (sh)
RU (1) RU2070884C1 (sh)
SG (1) SG47482A1 (sh)
SI (1) SI9110396B (sh)
SK (2) SK282407B6 (sh)
TN (1) TNSN91010A1 (sh)
UA (1) UA25969A1 (sh)
YU (1) YU48854B (sh)
ZA (1) ZA911611B (sh)
ZW (1) ZW2391A1 (sh)

Families Citing this family (51)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2674849B1 (fr) * 1991-04-02 1994-12-23 Logeais Labor Jacques Nouveaux derives de n-cyclohexyl benzamides ou thiobenzamides, leurs preparations et leurs applications en therapeutique.
WO1993005038A1 (en) * 1991-09-12 1993-03-18 Smithkline Beecham Plc 5-ht4 receptor antagonists
CA2129112A1 (en) * 1992-02-06 1993-08-19 Francis David King Benzopyran, benzothiopyran and benzofuran derivatives as 5-ht4 antagonists
US5595872A (en) * 1992-03-06 1997-01-21 Bristol-Myers Squibb Company Nucleic acids encoding microsomal trigyceride transfer protein
GB9219163D0 (en) * 1992-09-10 1992-10-28 Smithkline Beecham Plc Pharmaceuticals
JPH08502273A (ja) * 1992-10-13 1996-03-12 スミスクライン・ビーチャム・パブリック・リミテッド・カンパニー 5−ht▲下4▼レセプターアンタゴニスト用複素環式エステルまたはアミド
MX9306311A (es) * 1992-10-13 1994-04-29 Smithkline Beecham Plc Compuestos antagonistas del receptor de 5-ht4, procedimiento para su preparacion y composiciones farmaceuticas que los contienen
TW294595B (sh) * 1992-11-20 1997-01-01 Janssen Pharmaceutica Nv
GB9301660D0 (en) * 1993-01-28 1993-03-17 Smithkline Beecham Plc Pharmaceuticals
US5739135A (en) * 1993-09-03 1998-04-14 Bristol-Myers Squibb Company Inhibitors of microsomal triglyceride transfer protein and method
US5864039A (en) * 1994-03-30 1999-01-26 Yoshitomi Pharmaceutical Industries, Ltd. Benzoic acid compounds and use thereof as medicaments
JPH0820586A (ja) 1994-07-05 1996-01-23 Sanwa Kagaku Kenkyusho Co Ltd 1−アザビシクロ[3.3.0]オクタン誘導体、その塩及び製法並びに用途
GB9418326D0 (en) * 1994-09-12 1994-11-02 Lilly Industries Ltd Pharmaceutical compounds
JPH0873463A (ja) 1994-07-05 1996-03-19 Sanwa Kagaku Kenkyusho Co Ltd ベンゾピランカルボキサミド誘導体、その塩及び製法並びに用途
EP0784619B1 (en) * 1994-09-27 1999-03-24 Janssen Pharmaceutica N.V. Phenyl-oxo-alkyl-(4-piperidinyl)benzoate derivatives
PL182502B1 (pl) * 1994-09-27 2002-01-31 Janssen Pharmaceutica Nv Nowe związki, pochodne bicyklicznego benzoesanu N-podstawionego piperydynylu, środek farmaceutyczny i sposób wytwarzania pochodnych bicyklicznego benzoesanu N-podstawionego piperydynylu
TW490465B (en) * 1994-11-24 2002-06-11 Janssen Pharmaceutica Nv Enterokinetic benzamide, the preparation process and the pharmaceutical compositions thereof
US6096763A (en) * 1995-02-23 2000-08-01 Merck & Co., Inc. α1a adrenergic receptor antagonists
TW360653B (en) * 1995-03-01 1999-06-11 Janssen Pharmaceutica Nv A oxadiazole compound having colon motility stimulating properties, its preparation process and its pharmaceutical composition
GB9507882D0 (en) * 1995-04-18 1995-05-31 Pharmacia Spa Substituted dihydrobenzofuran derivatives as 5-ht4 agonists
GB2308362A (en) * 1995-12-19 1997-06-25 Lilly Industries Ltd Pharmaceutical indole derivatives
TW402591B (en) * 1997-07-11 2000-08-21 Janssen Pharmaceutica Nv Monocyclic benzamides of 3- or 4-substituted 4-(aminomethyl)-piperidine derivatives
CA2330475A1 (en) 1998-04-28 1999-11-04 Dainippon Pharmaceutical Co., Ltd. 1-¬(1-substituted-4-piperidinyl)methyl|-4-piperidine derivatives, process for producing the same, medicinal compositions containing the same and intermediates of these compounds
HRP20000750A2 (en) * 1998-05-14 2001-06-30 Egyt Gyogyszervegyeszeti Gyar Benzofuran derivatives, pharmaceutical composition containing the same, and a process for the preparation of the active ingredient
AU758807B2 (en) * 1998-09-10 2003-03-27 F. Hoffmann-La Roche Ag Dihydrobenzodioxine carboxamide and ketone derivatives as 5-HT4 receptor antagonists
JP2002530334A (ja) * 1998-11-23 2002-09-17 ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ 消化不良の処置用医薬の製造のためのプルカロプリドの使用
JO2181B1 (en) * 1999-04-29 2003-04-23 شركة جانسين فارماسوتيكا ان. في Procalopride solution is taken by mouth
SE9902987D0 (sv) 1999-08-24 1999-08-24 Astra Pharma Prod Novel compounds
CN1288730A (zh) * 1999-09-07 2001-03-28 麦克内尔-Ppc股份有限公司 轻泻组合物
GB0011838D0 (en) * 2000-05-17 2000-07-05 Astrazeneca Ab Chemical compounds
GB0104050D0 (en) 2001-02-19 2001-04-04 Astrazeneca Ab Chemical compounds
GB0107228D0 (en) 2001-03-22 2001-05-16 Astrazeneca Ab Chemical compounds
SE0103818D0 (sv) 2001-11-15 2001-11-15 Astrazeneca Ab Chemical compounds
CN1330646C (zh) * 2002-01-16 2007-08-08 詹森药业有限公司 普卢卡必利-n-氧化物
NZ535267A (en) * 2002-03-28 2006-03-31 Tanabe Seiyaku Co Benzofuran derivatives as inhibitors of blood coagulation factor X
AR040336A1 (es) 2002-06-26 2005-03-30 Glaxo Group Ltd Compuesto de piperidina, uso del mismo para la fabricacion de un medicamento, composicion farmaceutica que lo comprende y procedimiento para preparar dicho compuesto
SE0301369D0 (sv) 2003-05-09 2003-05-09 Astrazeneca Ab Chemical compounds
DE10349113A1 (de) * 2003-10-17 2005-05-12 Boehringer Ingelheim Pharma Verfahren zur Herstellung von Aminocrotonylverbindungen
EP1718639A2 (en) * 2004-02-27 2006-11-08 Vertex Pharmaceuticals Incorporated Caspase inhibitors and uses thereof
GB0525661D0 (en) * 2005-12-16 2006-01-25 Glaxo Group Ltd Novel compounds
PL2674428T3 (pl) * 2006-04-07 2017-01-31 Vertex Pharmaceuticals Incorporated Modulatory transporterów z kasetą wiążącą ATP
CN102477002B (zh) * 2010-11-26 2015-04-15 苏州凯达生物医药技术有限公司 3-氨基-2,2-双甲基丙酰胺的制备方法
PL2678332T3 (pl) 2011-02-25 2016-12-30 Pochodne diaminopirymidyny i sposoby ich wytwarzania
GB201103397D0 (sh) * 2011-02-28 2011-04-13 Shire Movetis N V
KR101256908B1 (ko) 2011-04-28 2013-04-23 (주)에이치비메디컬스 주름제거용 충전체
CN102295594B (zh) * 2011-07-12 2016-01-20 上海医药工业研究院 4-n-取代-1-(3-甲氧基丙基)-4-哌啶胺类化合物及制备和应用
CA2845039A1 (en) 2011-08-18 2013-02-21 Shire Ag Combinations of a 5-ht4 receptor agonist and a pde4 inhibitor for use in therapy
KR101657616B1 (ko) 2013-05-24 2016-09-19 주식회사유한양행 피리미딘 고리를 포함하는 바이사이클릭 유도체 및 그의 제조방법
EP3413891B1 (en) * 2016-02-11 2024-01-03 Symed Labs Limited Processes for the preparation of highly pure prucalopride succinate
CN110963999B (zh) * 2019-11-27 2021-05-11 广东东阳光药业有限公司 2,3-二氢苯并呋喃酰胺衍生物及其用途
WO2021225968A1 (en) * 2020-05-04 2021-11-11 Takeda Pharmaceutical Company Limited Luminally-acting n-(piperidin-4-yl)benzamide derivatives

Family Cites Families (28)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4186135A (en) * 1976-08-04 1980-01-29 Societe D'etudes Scientifiques Et Industrielles De L'ile-De-France Substituted 2,3-alkylene bis (oxy) benzamides and derivatives and method of preparation
FR2396757A2 (fr) * 1977-07-08 1979-02-02 Ile De France Nouveaux 2,3-alkylene bis (oxy) benzamides substitues, leurs derives et leurs procedes de preparation
FR2493848B2 (fr) * 1980-11-07 1986-05-16 Delalande Sa Nouveaux derives des nor-tropane et granatane, leur procede de preparation et leur application en therapeutique
EP0069481A1 (en) * 1981-06-17 1983-01-12 Beecham Group Plc Azabicycloalkyl benzamides, process for their preparation and pharmaceutical compositions containing them
EP0068700A1 (en) * 1981-06-29 1983-01-05 Beecham Group Plc Azobicycloalkylbenzamides, process for their preparation and pharmaceutical compositions containing them
US4962115A (en) * 1981-10-01 1990-10-09 Janssen Pharmaceutica N.V. Novel N-(3-hydroxy-4-piperidinyl)benzamide derivatives
CA1183847A (en) 1981-10-01 1985-03-12 Georges Van Daele N-(3-hydroxy-4-piperidinyl)benzamide derivatives
NZ203861A (en) * 1982-04-14 1986-07-11 Beecham Group Plc Bicyclic heterocyclic compounds and pharmaceutical compositions containing such
EP0108986A1 (en) * 1982-11-02 1984-05-23 Hokuriku Pharmaceutical Co.,Ltd N-substituted flavone-8-carboxamides
WO1984003281A1 (en) * 1983-02-19 1984-08-30 Beecham Group Plc Azabicycloalkyl benzamide and anilide derivatives
JPS59186969A (ja) * 1983-04-08 1984-10-23 Yoshitomi Pharmaceut Ind Ltd ベンゾフラン−およびベンゾピランカルボキサミド誘導体
US4888353A (en) * 1986-02-28 1989-12-19 Erbamont, Inc. Carboxamides useful as antiemetic or antipsychotic agents
CA1297877C (en) * 1983-12-22 1992-03-24 Daniel Lednicer Benzofurancarboxamides useful as antiemetic or antipsychotic agents
US4808624A (en) * 1984-06-28 1989-02-28 Bristol-Myers Company Pharmacologically active substituted benzamides
GB8519707D0 (en) * 1985-08-06 1985-09-11 Fordonal Sa Chemical compounds
GB8527052D0 (en) * 1985-11-02 1985-12-04 Beecham Group Plc Compounds
FR2593504B1 (fr) 1986-01-30 1988-12-09 Ile De France Nouveaux derives de dihydrobenzofuranne - et de chromane - carboxamides, leurs procedes de preparation et leur utilisation comme neuroleptiques
US4772459A (en) * 1986-09-09 1988-09-20 Erbamont, Inc. Method for controlling emesis caused by chemotherapeutic agents and antiemetic agents useful therein
US5130312A (en) * 1987-07-17 1992-07-14 Janssen Pharmaceutica N.V. Substituted N-(3-hydroxy-4-piperidinyl)benzamides
NZ225152A (en) 1987-07-17 1990-04-26 Janssen Pharmaceutica Nv Heterocyclically substituted piperidinyl benzamides as pharmaceuticals
US4906643A (en) * 1987-07-17 1990-03-06 Janssen Pharmaceutica N.V. Substituted N-(3-hydroxy-4-piperidinyl)benzamides as gastrointestinal agents
GB8718346D0 (en) * 1987-08-03 1987-09-09 Fordonal Sa Substituted benzamides
ZA886585B (en) * 1987-09-08 1990-05-30 Lilly Co Eli Specific 5-ht,antagonists
US5041454A (en) * 1987-09-25 1991-08-20 Janssen Pharmaceutica N.V. Novel substituted N-(1-alkyl-3-hydroxy-4-piperidinyl)benzamides
US4975439A (en) * 1987-09-25 1990-12-04 Janssen Pharmaceutical N.V. Novel substituted N-(1-alkyl-3-hydroxy-4-piperidinyl)benzamides
CA1317940C (en) 1987-09-25 1993-05-18 Georges H. P. Van Daele Substituted n-(1-alkyl-3-hydroxy-4-piperidinyl)benzamides
US4863921A (en) * 1988-04-27 1989-09-05 Rorer Pharmaceutical Corporation Dibenzofurancarboxamides and their pharmaceutical compositions and methods
US5374637A (en) * 1989-03-22 1994-12-20 Janssen Pharmaceutica N.V. N-(3-hydroxy-4-piperidinyl)(dihydrobenzofuran, dihydro-2H-benzopyran or dihydrobenzodioxin)carboxamide derivatives

Also Published As

Publication number Publication date
FI911096A0 (fi) 1991-03-05
PL168693B1 (pl) 1996-03-29
TNSN91010A1 (fr) 1992-10-25
FI101622B (fi) 1998-07-31
EP0445862A2 (en) 1991-09-11
HU910706D0 (en) 1991-09-30
HRP930483A2 (en) 1995-12-31
KR910016744A (ko) 1991-11-05
HK1010727A1 (en) 1999-06-25
SG47482A1 (en) 1998-04-17
IL97018A0 (en) 1992-03-29
LTIP846A (en) 1995-02-27
LV10085A (lv) 1994-05-10
FI911096A7 (fi) 1991-09-07
AU7207991A (en) 1991-09-12
CN1038936C (zh) 1998-07-01
DE69132119D1 (de) 2000-05-25
GR3033461T3 (en) 2000-09-29
CN1054598A (zh) 1991-09-18
HUT60733A (en) 1992-10-28
MY108831A (en) 1996-11-30
CA2037575A1 (en) 1991-09-07
PL168811B1 (pl) 1996-04-30
PT96937B (pt) 1998-07-31
PT96937A (pt) 1991-10-31
NO910863D0 (no) 1991-03-05
PL289323A1 (en) 1992-03-09
NO177424C (no) 1995-09-13
IL97018A (en) 1995-11-27
SI9110396A (en) 1997-12-31
CS46091A3 (en) 1991-10-15
CY2235B1 (en) 2003-07-04
KR0177521B1 (ko) 1999-03-20
LV10085B (en) 1995-02-20
YU39691A (sh) 1994-06-10
MA22076A1 (fr) 1991-10-01
US5262418A (en) 1993-11-16
PL168384B1 (en) 1996-02-29
SI9110396B (sl) 2000-06-30
JP2601566B2 (ja) 1997-04-16
RU2070884C1 (ru) 1996-12-27
PL169238B1 (pl) 1996-06-28
GB9005014D0 (en) 1990-05-02
NO910863L (no) 1991-09-09
CZ286617B6 (cs) 2000-05-17
EP0445862A3 (en) 1992-05-20
BG93979A (bg) 1993-12-24
EP0445862B1 (en) 2000-04-19
HU221627B1 (hu) 2002-12-28
HRP930483B1 (en) 2001-04-30
LT3708B (en) 1996-02-26
JPH04211685A (ja) 1992-08-03
DK0445862T3 (da) 2000-09-04
ZW2391A1 (en) 1992-09-07
US5185335A (en) 1993-02-09
NZ237189A (en) 1992-11-25
ZA911611B (en) 1992-11-25
IE910710A1 (en) 1991-09-11
SK282406B6 (sk) 2002-01-07
ATE191912T1 (de) 2000-05-15
SK282407B6 (sk) 2002-01-07
FI101622B1 (fi) 1998-07-31
PL168356B1 (pl) 1996-02-29
NO177424B (no) 1995-06-06
PL168686B1 (pl) 1996-03-29
UA25969A1 (uk) 1999-02-26
CA2037575C (en) 2003-09-16
HU211350A9 (en) 1995-11-28
BG60381B1 (bg) 1995-01-31
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DE69132119T2 (de) 2000-12-21
AU636012B2 (en) 1993-04-08

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