FI102753B1 - Menetelmä uusien, terapeuttisesti käyttökelpoisten substituoitujen tiatsolyyli- ja pyridinyylijohdannaisten valmistamiseksi - Google Patents

Menetelmä uusien, terapeuttisesti käyttökelpoisten substituoitujen tiatsolyyli- ja pyridinyylijohdannaisten valmistamiseksi

Info

Publication number
FI102753B1
FI102753B1 FI930199A FI930199A FI102753B1 FI 102753 B1 FI102753 B1 FI 102753B1 FI 930199 A FI930199 A FI 930199A FI 930199 A FI930199 A FI 930199A FI 102753 B1 FI102753 B1 FI 102753B1
Authority
FI
Finland
Prior art keywords
formula
alk
preparation
substituted thiazolyl
radical
Prior art date
Application number
FI930199A
Other languages
English (en)
Finnish (fi)
Swedish (sv)
Other versions
FI930199A0 (fi
FI102753B (fi
FI930199A7 (fi
Inventor
Frans Eduard Janssens
Francois Maria Sommen
Gaston Stanislas Marcell Diels
Original Assignee
Janssen Pharmaceutica Nv
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 Nv filed Critical Janssen Pharmaceutica Nv
Publication of FI930199A0 publication Critical patent/FI930199A0/fi
Publication of FI930199A7 publication Critical patent/FI930199A7/fi
Application granted granted Critical
Publication of FI102753B publication Critical patent/FI102753B/fi
Publication of FI102753B1 publication Critical patent/FI102753B1/fi

Links

Classifications

    • 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • A61P37/08Antiallergic agents
    • 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
    • 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
    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D473/00Heterocyclic compounds containing purine ring systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D473/00Heterocyclic compounds containing purine ring systems
    • C07D473/26Heterocyclic compounds containing purine ring systems with an oxygen, sulphur, or nitrogen atom directly attached in position 2 or 6, but not in both
    • C07D473/28Oxygen atom
    • C07D473/30Oxygen atom attached in position 6, e.g. hypoxanthine
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D473/00Heterocyclic compounds containing purine ring systems
    • C07D473/40Heterocyclic compounds containing purine ring systems with halogen atoms or perhalogeno-alkyl radicals directly attached in position 2 or 6
    • 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

Landscapes

  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Veterinary Medicine (AREA)
  • Engineering & Computer Science (AREA)
  • Public Health (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Immunology (AREA)
  • Pulmonology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Thiazole And Isothizaole Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
FI930199A 1990-07-19 1993-01-18 Menetelmä uusien, terapeuttisesti käyttökelpoisten substituoitujen tiatsolyyli- ja pyridinyylijohdannaisten valmistamiseksi FI102753B1 (fi)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US55432590A 1990-07-19 1990-07-19
PCT/EP1991/001292 WO1992001697A1 (en) 1990-07-19 1991-07-09 Novel substituted thiazolyl and substituted pyridinyl derivatives

Publications (4)

Publication Number Publication Date
FI930199A0 FI930199A0 (fi) 1993-01-18
FI930199A7 FI930199A7 (fi) 1993-01-18
FI102753B FI102753B (fi) 1999-02-15
FI102753B1 true FI102753B1 (fi) 1999-02-15

Family

ID=24212925

Family Applications (1)

Application Number Title Priority Date Filing Date
FI930199A FI102753B1 (fi) 1990-07-19 1993-01-18 Menetelmä uusien, terapeuttisesti käyttökelpoisten substituoitujen tiatsolyyli- ja pyridinyylijohdannaisten valmistamiseksi

Country Status (27)

Country Link
EP (1) EP0539420B1 (enExample)
JP (1) JP3085707B2 (enExample)
KR (1) KR100206723B1 (enExample)
CN (1) CN1037770C (enExample)
AT (1) ATE188477T1 (enExample)
AU (1) AU646280B2 (enExample)
CA (1) CA2086546A1 (enExample)
CZ (1) CZ279903B6 (enExample)
DE (1) DE69131895T2 (enExample)
DK (1) DK0539420T3 (enExample)
ES (1) ES2142802T3 (enExample)
FI (1) FI102753B1 (enExample)
GR (1) GR3032999T3 (enExample)
HU (1) HU221298B1 (enExample)
IE (1) IE912533A1 (enExample)
IL (1) IL98865A (enExample)
MX (1) MX9100307A (enExample)
NO (1) NO304791B1 (enExample)
NZ (1) NZ238863A (enExample)
PH (1) PH31063A (enExample)
PL (1) PL170580B1 (enExample)
PT (1) PT98366B (enExample)
RU (1) RU2067978C1 (enExample)
SK (1) SK280690B6 (enExample)
TW (1) TW209217B (enExample)
WO (1) WO1992001697A1 (enExample)
ZA (1) ZA915654B (enExample)

Families Citing this family (23)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ES2048109B1 (es) * 1992-07-20 1994-12-16 Espanola Prod Quimicos Procedimiento de preparacion de nuevos derivados piperidicos del bencimidazol.
US6211199B1 (en) 1995-11-17 2001-04-03 Aventis Pharmaceuticals Inc. Substituted 4-(1H-benzimidazol-2-yl-amino)piperidines useful for the treatment of allergic diseases
US6423704B2 (en) 1995-12-20 2002-07-23 Aventis Pharmaceuticals Inc. Substituted 4-(1H-benzimidazol-2-yl)[1,4]diazepanes useful for the treatment of allergic diseases
US6194406B1 (en) 1995-12-20 2001-02-27 Aventis Pharmaceuticals Inc. Substituted 4-(1H-benzimidazol-2-yl)[1,4]diazepanes useful for the treatment of allergic disease
US5922737A (en) * 1996-02-21 1999-07-13 Hoechst Marion Roussel, Inc. Substituted N-methyl-N-(4-(4-(1H-Benzimidazol-2-YL-amino) piperidin-1-YL)-2-(arlyl) butyl) benzamides useful for the treatment of allergic diseases
US5932571A (en) * 1996-02-21 1999-08-03 Hoechst Marion Roussel, Inc. Substituted N-methyl-N-(4-(4-(1H-benzimidazol-2-yl) {1,4}diazepan-1-yl)-2-(aryl) butyl) benzamides useful for the treatment of allergic diseases
US5998439A (en) * 1996-02-21 1999-12-07 Hoescht Marion Roussel, Inc. Substituted N-methyl-N-(4-(piperidin-1-yl)-2-(aryl)butyl)benzamides useful for the treatment of allergic diseases
DK1196409T3 (da) * 1999-06-28 2004-06-07 Janssen Pharmaceutica Nv Respiratoriske syncytilvirusreplikationsinhibitorer
HRP20010934A2 (en) * 1999-06-28 2003-06-30 Janssen Pharmaceutica Nv Respiratory syncytial virus replication inhibitors
SK18942001A3 (sk) * 1999-06-28 2002-10-08 Janssen Pharmaceutica N. V. Inhibítory replikácie respiračného syncytiálneho vírusu
CZ20021210A3 (cs) * 1999-10-08 2002-08-14 Grünenthal GmbH Bicyklické deriváty imidazo-3-yl-aminu, způsob jejich výroby, jejich pouľití a léčiva tyto látky obsahující
PT1599468E (pt) 2003-01-14 2008-01-14 Arena Pharm Inc Derivados de arilo e heteroarilo 1,2,3.-trissubstituídos comomoduladores do metabolismo, e profilaxia e tratamento dedesordens relacionadas tais como diabetes e hiperglicemia
AR045047A1 (es) 2003-07-11 2005-10-12 Arena Pharm Inc Derivados arilo y heteroarilo trisustituidos como moduladores del metabolismo y de la profilaxis y tratamiento de desordenes relacionados con los mismos
RU2239637C1 (ru) * 2003-07-17 2004-11-10 Дж.Б.Кемикалс Энд Фармасьютикалс Лтд. Улучшенный способ получения 5-[2-этокси-5-(4-метилпиперазин-1-илсульфонил)фенил]-1 метил-3-н-пропил-1,6-дигидро-7h-пиразол [4,3-d] пиримидин-7-она
RU2264814C2 (ru) * 2003-12-29 2005-11-27 Открытое акционерное общество "Химико-фармацевтический комбинат "АКРИХИН" (ОАО "АКРИХИН") Антигистаминная фармацевтическая композиция
ES2340179T3 (es) * 2004-05-12 2010-05-31 Bristol-Myers Squibb Company Antagonistas de urea del receptor p2y1 utiles en el tratamiento de afecciones tromboticas.
DE102004044884A1 (de) * 2004-09-14 2006-05-24 Grünenthal GmbH Substituierte bizyklische Imidazo-3-yl-amin-Verbindungen
DOP2006000010A (es) 2005-01-10 2006-07-31 Arena Pharm Inc Procedimiento para preparar eteres aromáticos
JP5941916B2 (ja) 2010-09-22 2016-06-29 アリーナ ファーマシューティカルズ, インコーポレイテッド Gpr119レセプターのモジュレーターおよびそれに関連する障害の処置
EP3040334A1 (en) * 2014-12-29 2016-07-06 Faes Farma, S.A. New benzimidazole derivatives as antihistamine agents
PL3242666T3 (pl) 2015-01-06 2025-02-17 Arena Pharmaceuticals, Inc. Związek do zastosowania w leczeniu dolegliwości związanych z receptorem s1p1
DK3310760T3 (da) 2015-06-22 2022-10-24 Arena Pharm Inc Krystallinsk L-argininsalt af (R)-2-(7-(4-cyclopentyl-3-(trifluormethyl)benzyloxy)-1,2,3,4-tetrahydrocyclopenta[b]indol-3- yl)eddikesyre til anvendelse ved S1P1-receptor-associerede lidelser
BR112020024762A2 (pt) 2018-06-06 2021-03-23 Arena Pharmaceuticals, Inc. métodos de tratamento de condições relacionadas ao receptor s1p1

Family Cites Families (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4556660A (en) * 1982-07-12 1985-12-03 Janssen Pharmaceutica N.V. N-(Bicyclic heterocyclyl)-4-piperidinamines
US4634704A (en) * 1983-10-06 1987-01-06 Janssen Pharmaceutica, N.V. Anti-allergic five membered heterocyclic ring containing N-(bicyclic heterocycyl)-4-piperidinamines
US4695569A (en) * 1983-11-30 1987-09-22 Janssen Pharmaceutica N.V. Bicyclic heterocyclyl containing N-(bicyclic heterocyclyl)-4-piperidinamines
US4588722A (en) * 1984-01-09 1986-05-13 Janssen Pharmaceutica N.V. N-(4-piperidinyl) bicyclic condensed 2-imidazolamine derivatives
US4695575A (en) * 1984-11-13 1987-09-22 Janssen Pharmaceutica, N.V. 4-[(bicycle heterocyclyl)-methyl and -hetero]-piperidines
GB8515934D0 (en) * 1985-06-24 1985-07-24 Janssen Pharmaceutica Nv (4-piperidinomethyl and-hetero)purines
US4835161A (en) * 1986-02-03 1989-05-30 Janssen Pharmaceutica N.V. Anti-histaminic compositions containing n-heterocyclyl-4-piperidinamines
DE3701863A1 (de) * 1987-01-23 1988-08-04 Standard Elektrik Lorenz Ag Sender zur kohaerent optischen nachrichtenuebertragung
US4897401A (en) * 1987-06-19 1990-01-30 Janssen Pharmaceutical N.V. N-(4-piperidinyl) bicyclic condensed 2-imidazolamine derivatives useful in treating allergic diseases
CA1317939C (en) * 1987-07-01 1993-05-18 Janssen Pharmaceutica Naamloze Vennootschap ¬(bicyclic heterocyclyl)methyl and -hetero| substituted hexahydro-1h-azepines and pyrrolidines
GB8900380D0 (en) * 1989-01-09 1989-03-08 Janssen Pharmaceutica Nv 2-aminopyrimidinone derivatives

Also Published As

Publication number Publication date
NZ238863A (en) 1993-03-26
JP3085707B2 (ja) 2000-09-11
PL297612A1 (enExample) 1992-07-13
HU9300096D0 (en) 1993-04-28
MX9100307A (es) 1992-02-28
EP0539420A1 (en) 1993-05-05
PT98366A (pt) 1992-05-29
HUT64066A (en) 1993-11-29
FI930199A0 (fi) 1993-01-18
PT98366B (pt) 1999-01-29
AU8209391A (en) 1992-02-18
CZ279903B6 (cs) 1995-08-16
SK280690B6 (sk) 2000-06-12
NO930139D0 (no) 1993-01-15
FI102753B (fi) 1999-02-15
IL98865A0 (en) 1992-07-15
CN1058216A (zh) 1992-01-29
ES2142802T3 (es) 2000-05-01
GR3032999T3 (en) 2000-07-31
EP0539420B1 (en) 2000-01-05
DE69131895D1 (de) 2000-02-10
FI930199A7 (fi) 1993-01-18
HU221298B1 (en) 2002-09-28
TW209217B (enExample) 1993-07-11
IL98865A (en) 1995-11-27
DE69131895T2 (de) 2000-07-20
WO1992001697A1 (en) 1992-02-06
CS223991A3 (en) 1992-02-19
JPH05508638A (ja) 1993-12-02
RU2067978C1 (ru) 1996-10-20
AU646280B2 (en) 1994-02-17
KR100206723B1 (ko) 1999-07-01
IE912533A1 (en) 1992-01-29
NO304791B1 (no) 1999-02-15
PL170580B1 (pl) 1997-01-31
DK0539420T3 (da) 2000-05-29
PH31063A (en) 1998-02-05
ZA915654B (en) 1993-03-31
ATE188477T1 (de) 2000-01-15
CN1037770C (zh) 1998-03-18
CA2086546A1 (en) 1992-01-20
NO930139L (no) 1993-01-15

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