NO169900C - Analogifremgangsmaate for fremstilling av terapeutisk aktive (ih-azol-1-ylmetyl)substituerte benzotriazolderivater - Google Patents

Analogifremgangsmaate for fremstilling av terapeutisk aktive (ih-azol-1-ylmetyl)substituerte benzotriazolderivater

Info

Publication number
NO169900C
NO169900C NO882390A NO882390A NO169900C NO 169900 C NO169900 C NO 169900C NO 882390 A NO882390 A NO 882390A NO 882390 A NO882390 A NO 882390A NO 169900 C NO169900 C NO 169900C
Authority
NO
Norway
Prior art keywords
azol
ylmethyl
preparation
therapeutic active
analogue procedure
Prior art date
Application number
NO882390A
Other languages
English (en)
Norwegian (no)
Other versions
NO882390D0 (no
NO882390L (no
NO169900B (no
Inventor
Alfons Herman Marg Raeymaekers
Eddy Jean Edgard Freyne
Josephus Ludovicus Hube Gelder
Marc Gaston Venet
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 NO882390D0 publication Critical patent/NO882390D0/no
Publication of NO882390L publication Critical patent/NO882390L/no
Publication of NO169900B publication Critical patent/NO169900B/no
Publication of NO169900C publication Critical patent/NO169900C/no

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/06Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D231/00Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • 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
    • 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
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D233/00Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/54Heterocyclic 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
    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D249/00Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
    • C07D249/02Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
    • C07D249/081,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
NO882390A 1987-06-01 1988-05-31 Analogifremgangsmaate for fremstilling av terapeutisk aktive (ih-azol-1-ylmetyl)substituerte benzotriazolderivater NO169900C (no)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US5602187A 1987-06-01 1987-06-01

Publications (4)

Publication Number Publication Date
NO882390D0 NO882390D0 (no) 1988-05-31
NO882390L NO882390L (no) 1988-12-02
NO169900B NO169900B (no) 1992-05-11
NO169900C true NO169900C (no) 1992-08-19

Family

ID=22001654

Family Applications (1)

Application Number Title Priority Date Filing Date
NO882390A NO169900C (no) 1987-06-01 1988-05-31 Analogifremgangsmaate for fremstilling av terapeutisk aktive (ih-azol-1-ylmetyl)substituerte benzotriazolderivater

Country Status (24)

Country Link
EP (1) EP0293978B1 (ja)
JP (1) JPH0662612B2 (ja)
KR (1) KR970000952B1 (ja)
CN (1) CN1022184C (ja)
AU (1) AU603446B2 (ja)
BG (2) BG50278A3 (ja)
CA (1) CA1307271C (ja)
CY (1) CY1866A (ja)
DE (1) DE3884055T2 (ja)
DK (1) DK175218B1 (ja)
ES (1) ES2059490T3 (ja)
FI (1) FI90078C (ja)
HK (1) HK114795A (ja)
HU (2) HU201056B (ja)
IE (1) IE61823B1 (ja)
IL (1) IL86551A (ja)
LT (1) LT3950B (ja)
LV (1) LV10452B (ja)
NO (1) NO169900C (ja)
NZ (1) NZ224714A (ja)
PT (1) PT87623B (ja)
RU (1) RU1838308C (ja)
UA (1) UA11192A (ja)
ZA (1) ZA883861B (ja)

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GB8827820D0 (en) * 1988-11-29 1988-12-29 Janssen Pharmaceutica Nv (1h-azol-1-ylmethyl)substituted quinoline derivatives
CA2002859C (en) * 1988-11-29 1998-12-29 Jean P. F. Van Wauwe Method of treating epithelial disorders
US5157046A (en) * 1988-11-29 1992-10-20 Janssen Pharmaceutica N.V. Method of treating epithelial disorders
EP0408509B1 (de) * 1989-07-14 1996-03-06 Ciba-Geigy Ag Substituierte Benzonitrile
US5066656A (en) * 1989-11-01 1991-11-19 Janssen Pharmaceutica N.V. Pharmacologically active (6,7-dihydro-5H-pyrrolo[1,2-c]imidazol-5-yl)- and (5,6,7,8-tetrahydroimidazo[1,5-a]pyridin-5-yl) substituted 1H-benzotriazole derivatives
CA2026792A1 (en) * 1989-11-01 1991-05-02 Michael N. Greco (6,7-dihydro-5h-pyrrolo[1,2-c]imidazol-5-yl)- and (5,6,7,8-tetrahydroimidazo[1,5-a]pyridin-5-yl) substituted 1h-benzotriazole derivatives
NZ236440A (en) * 1989-12-15 1993-07-27 Merck & Co Inc Reversal of sexual phenotype in poultry using an inhibitor of steroid biotransformation and/or aromatase inhibitor, poultry produced by this process
AU7124691A (en) * 1990-02-27 1991-08-29 Ciba-Geigy Ag Benzofurans
DE4010797A1 (de) * 1990-04-04 1991-10-10 Hoechst Ag Substituierte azole, verfahren zu deren herstellung, diese enthaltende mittel und deren verwendung
EP0457716A1 (de) * 1990-04-20 1991-11-21 Ciba-Geigy Ag Naphthalinderivate
TW224461B (ja) * 1990-09-18 1994-06-01 Ciba Geigy Ag
US5162337A (en) * 1990-10-05 1992-11-10 Merck & Co., Inc. Animal growth promotion
TW210334B (ja) * 1990-12-12 1993-08-01 Ciba Geigy Ag
CH683151A5 (de) * 1991-04-24 1994-01-31 Ciba Geigy Ag Antikonzeption bei weiblichen Primaten ohne Beeinflussung des menstruellen Zyklus.
ES2139605T3 (es) 1991-09-02 2000-02-16 Yamanouchi Pharma Co Ltd Amina terciaria triazolilada o una sal de esta.
US5635521A (en) * 1991-09-23 1997-06-03 Sandoz Ltd. Imidazolylmethyl-pyridines
JP2700595B2 (ja) * 1992-05-21 1998-01-21 呉羽化学工業株式会社 アゾール誘導体を含有する抗アロマターゼ剤
NZ257551A (en) * 1992-11-10 1995-10-26 Janssen Pharmaceutica Nv Preparation of 6-[(4-chlorophenyl)(1h-1,2,4-triazol-1-yl)methyl]-1-methyl-1h-benzotriazole in enantiomerically pure form;intermediates
EP0684235A1 (en) * 1994-05-27 1995-11-29 Mochida Pharmaceutical Co., Ltd. Novel azolyl methyl phenyl derivatives having aromatase inhibitory activity
WO1997006788A1 (en) * 1995-08-14 1997-02-27 Janssen Pharmaceutica N.V. Transdermal administration of vorozole
IT1286866B1 (it) * 1996-10-28 1998-07-17 Menarini Farma Ind Composti furano-eterociclici,loro preparazione ed uso come inibitori di aromatasi
EP0949242A4 (en) * 1996-12-24 2004-09-08 Chugai Seiyakukabushiki Kaisha AROMATIC AMINE DERIVATIVES HAVING AN INHIBITORY ACTION WITH RESPECT TO OUR
EP1295880A4 (en) * 2000-06-28 2004-05-06 Ssp Co Ltd IMIDAZOLE DERIVATIVES OR SALTS THEREOF, AND MEDICINAL PRODUCTS CONTAINING DERIVATIVES OR SALTS
US7135575B2 (en) 2003-03-03 2006-11-14 Array Biopharma, Inc. P38 inhibitors and methods of use thereof
PL214032B1 (pl) * 2003-03-03 2013-06-28 Array Biopharma Zwiazki bedace inhibitorami kinazy p38, kompozycja farmaceutyczna je zawierajaca oraz ich zastosowanie do wytwarzania leku do leczenia stanu, w którym posredniczy kinaza p38
MX2007008781A (es) 2005-01-21 2007-09-11 Astex Therapeutics Ltd Compuestos farmaceuticos.
ES2329614T3 (es) * 2005-04-29 2009-11-27 Janssen Pharmaceutica Nv Derivados de benzotriazol como antagonistas de los receptores cannabinoides.
US7572807B2 (en) * 2005-06-09 2009-08-11 Bristol-Myers Squibb Company Heteroaryl 11-beta-hydroxysteroid dehydrogenase type I inhibitors
EP1934241B1 (en) 2005-09-15 2012-11-14 Council of Scientific and Industrial Research Novel series of imidazolyl substituted steroidal and indan-1-one derivatives
PL1981851T3 (pl) 2006-01-31 2012-07-31 Array Biopharma Inc Inhibitory kinazy i sposoby ich stosowania
WO2008044041A1 (en) 2006-10-12 2008-04-17 Astex Therapeutics Limited Pharmaceutical combinations
JP5528807B2 (ja) 2006-10-12 2014-06-25 アステックス、セラピューティックス、リミテッド 複合薬剤
EP2630136A1 (en) * 2010-10-21 2013-08-28 Universität des Saarlandes Selective cyp11b1 inhibitors for the treatment of cortisol dependent diseases

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GR75101B (ja) * 1980-10-23 1984-07-13 Pfizer
US4609666A (en) * 1984-06-18 1986-09-02 Eli Lilly And Company Aromatase inhibiting derivatives of α,α-bis(4-halophenyl)methyltetrazoles and triazoles
US4801594A (en) * 1984-06-18 1989-01-31 Eli Lilly And Company Aromatase inhibitors
EP0165781A1 (en) * 1984-06-18 1985-12-27 Eli Lilly And Company Aromatase inhibiting N-substituted imidazole derivatives
US4602025A (en) * 1984-06-18 1986-07-22 Eli Lilly And Company Aromatase inhibitors
US4659730A (en) * 1984-06-18 1987-04-21 Eli Lilly And Company Aromatase inhibiting imidazole derivatives
DE3744589C1 (de) 1987-12-31 1988-12-29 Albrecht Josef Bohrfutter Nachspannendes Bohrfutter

Also Published As

Publication number Publication date
NZ224714A (en) 1990-03-27
FI90078B (fi) 1993-09-15
CN88103408A (zh) 1988-12-14
DK295288D0 (da) 1988-05-31
EP0293978A2 (en) 1988-12-07
FI90078C (fi) 1993-12-27
CY1866A (en) 1988-05-26
ES2059490T3 (es) 1994-11-16
KR890000469A (ko) 1989-03-14
IL86551A (en) 1992-07-15
UA11192A (uk) 1996-12-25
AU603446B2 (en) 1990-11-15
EP0293978B1 (en) 1993-09-15
EP0293978A3 (en) 1990-06-13
IE61823B1 (en) 1994-11-30
PT87623A (pt) 1988-06-01
DE3884055D1 (de) 1993-10-21
LTIP1625A (en) 1995-07-25
DE3884055T2 (de) 1994-01-27
BG50278A3 (en) 1992-06-15
HUT49132A (en) 1989-08-28
LV10452A (lv) 1995-02-20
FI882552A0 (fi) 1988-05-31
CN1022184C (zh) 1993-09-22
DK295288A (da) 1988-12-02
NO882390D0 (no) 1988-05-31
LV10452B (en) 1995-08-20
HU201056B (en) 1990-09-28
PT87623B (pt) 1992-09-30
NO882390L (no) 1988-12-02
AU1653788A (en) 1988-12-01
JPH0662612B2 (ja) 1994-08-17
KR970000952B1 (ko) 1997-01-21
IL86551A0 (en) 1988-11-15
BG60429B2 (bg) 1995-03-31
JPS63316775A (ja) 1988-12-26
NO169900B (no) 1992-05-11
FI882552A (fi) 1988-12-02
HK114795A (en) 1995-07-21
CA1307271C (en) 1992-09-08
LT3950B (en) 1996-05-27
DK175218B1 (da) 2004-07-12
IE881640L (en) 1988-12-01
ZA883861B (en) 1990-01-31
RU1838308C (ru) 1993-08-30
HU211482A9 (en) 1995-11-28

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Legal Events

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MK1K Patent expired