FI92696B - Förfarande för framställning av terapeutiskt användbara tiazolidindionderivat - Google Patents

Förfarande för framställning av terapeutiskt användbara tiazolidindionderivat Download PDF

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Publication number
FI92696B
FI92696B FI904413A FI904413A FI92696B FI 92696 B FI92696 B FI 92696B FI 904413 A FI904413 A FI 904413A FI 904413 A FI904413 A FI 904413A FI 92696 B FI92696 B FI 92696B
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FI
Finland
Prior art keywords
methyl
formula
phenyl
oxazolyl
bond
Prior art date
Application number
FI904413A
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English (en)
Finnish (fi)
Other versions
FI904413A0 (sv
FI92696C (sv
Inventor
Bernard Hulin
David A Clark
Steven W Goldstein
Original Assignee
Pfizer
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 Pfizer filed Critical Pfizer
Publication of FI904413A0 publication Critical patent/FI904413A0/sv
Publication of FI92696B publication Critical patent/FI92696B/sv
Application granted granted Critical
Publication of FI92696C publication Critical patent/FI92696C/sv

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    • 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
    • C07D263/00Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
    • C07D263/02Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
    • C07D263/30Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D263/34Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having two or three 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
    • C07D263/44Two oxygen atoms
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/06Antihyperlipidemics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/08Drugs for disorders of the metabolism for glucose homeostasis
    • 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
    • C07D417/02Heterocyclic 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 two hetero rings
    • C07D417/12Heterocyclic 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 two hetero rings linked by a chain containing hetero atoms as chain links

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Diabetes (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Hematology (AREA)
  • Obesity (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Emergency Medicine (AREA)
  • Endocrinology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Thiazole And Isothizaole Compounds (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
  • Cleaning Or Clearing Of The Surface Of Open Water (AREA)
  • Treatment Of Fiber Materials (AREA)

Claims (5)

1. Förfarande för framställning av en terapeutiskt användbar förening med formeln
5 K T <CIVn V / \ 1 (I) z väri den streckade Iinjen betecknar en bindning eller ingen bindning; V är -CH=CH-;
15 W är S, SO, S02, SOjNR1, NR^Oj, CONR1 eller NR^O; X är 0; Y är N, varvid en oxazol-4-ylgrupp bildas; Z är 2-fenyl; Z1 är 5-metyl;
20 R1 är självständigt väte eller (01-4) -alkyl; och n är 1 eller 2; ett farmaceutiskt godtagbart katjonsalt därav; eller ett farmaceutiskt godtagbart syraadditionssalt därav, när fö- reningen innehäller basiskt kväve; kännetecknat ...25 därav, att • · · a) när den streckade Iinjen betecknar en bindning, kondenseras tiazolidin-2,4-dion med en aldehyd eller keton med formeln
30 H .... .J-.r 35 92696 b) och när den streckade linjen icke betecknar en bindning, reduceras den ovan framställda föreningen med formeln (I), vari den streckade linjen betecknar en bindning; 5 c) när W är SOjNR1 eller CONR1 omsätts en aktiverad form av en syra med formeln />ch2V X^C ^SO,H -H, eller JCH2'n X'^S C02H -to?.. med en amin med formeln 0 20 ____ R j \„ eller HN / n1 25 - · · d) när W är NRxS02 eller NR^O, omsätts en aktiverad form av en syra med formeln 0 s—Λ) HOOC 35 eller • < II 92696 xVKi: b H0S02 v 0 med en amin med formeln 10 (CH ) 15 och, om önskvärt e) omvandlas en ovan framställd förening med formeln (I) till ett farmaceutiskt godtagbart katjonsalt; f) omvandlas en ovan framställd förening med formeln (I) vilken innehäller basiskt kväve, till ett far- 20 maceutiskt godtagbart syraadditionssalt; g) oxideras en ovan framställd förening med formeln (I), väri W är S, för bildande av en förening med formeln (I), väri W är SO eller S02.
2. Förfarande enligt patentkravet 1, känne-25 tecknat därav, att den streckade linjen icke be- tecknar en bindning.
3. Förfarande enligt patentkravet 2, känne-tecknat därav, att n är 1, W är CONR1.
4. Förfarande enligt patentkravet 2, känne-30 tecknat därav, att n är 1, W är NRxC0.
5. Förfarande enligt patentkravet 2, känne-tecknat därav, att n är 2, W är S eller S02. • .
FI904413A 1988-03-08 1990-09-07 Förfarande för framställning av terapeutiskt användbara tiazolidindionderivat FI92696C (sv)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
PCT/US1988/000745 WO1989008652A1 (en) 1988-03-08 1988-03-08 Thiazolidinedione derivatives as hypoglycemic agents
US8800745 1988-03-08

Publications (3)

Publication Number Publication Date
FI904413A0 FI904413A0 (sv) 1990-09-07
FI92696B true FI92696B (sv) 1994-09-15
FI92696C FI92696C (sv) 1994-12-27

Family

ID=22208591

Family Applications (1)

Application Number Title Priority Date Filing Date
FI904413A FI92696C (sv) 1988-03-08 1990-09-07 Förfarande för framställning av terapeutiskt användbara tiazolidindionderivat

Country Status (17)

Country Link
EP (1) EP0389699B1 (sv)
JP (1) JPH01299289A (sv)
KR (1) KR910000734B1 (sv)
CN (1) CN1026234C (sv)
AU (1) AU594899B2 (sv)
CA (1) CA1328265C (sv)
DK (1) DK108789A (sv)
ES (3) ES2052906T3 (sv)
FI (1) FI92696C (sv)
HU (1) HU217432B (sv)
IL (1) IL89481A (sv)
MY (1) MY103837A (sv)
NO (1) NO178068C (sv)
NZ (1) NZ228247A (sv)
PT (1) PT89922B (sv)
WO (1) WO1989008652A1 (sv)
ZA (1) ZA891681B (sv)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7026334B1 (en) 1999-07-26 2006-04-11 Shionogi & Co., Ltd. Thiazolidine compounds and pharmaceutical compositions exhibiting thrombopoietin receptor agonism

Families Citing this family (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
MX15171A (es) * 1988-03-08 1993-05-01 Pfizer Derivados de tiazolidinodiona hipoglicemicos
GB8919417D0 (en) * 1989-08-25 1989-10-11 Beecham Group Plc Novel compounds
US5089514A (en) * 1990-06-14 1992-02-18 Pfizer Inc. 3-coxazolyl [phenyl, chromanyl or benzofuranyl]-2-hydroxypropionic acid derivatives and analogs as hypoglycemic agents
AU645112B2 (en) * 1990-08-23 1994-01-06 Pfizer Inc. Hypoglycemic hydroxyurea derivatives
FR2696743B1 (fr) * 1992-10-12 1994-12-23 Adir Nouveaux composés de thiazolidine dione, leur procédé de préparation et les compositions pharmaceutiques les contenant.
DE4317320A1 (de) * 1993-05-25 1994-12-01 Boehringer Mannheim Gmbh Neue Thiazolidindione und diese enthaltende Arzneimittel
JPH08157473A (ja) * 1994-10-06 1996-06-18 Nissan Chem Ind Ltd ピラゾール系チアゾリジン類
US5641796A (en) * 1994-11-01 1997-06-24 Eli Lilly And Company Oral hypoglycemic agents
JP3906935B2 (ja) * 1995-12-18 2007-04-18 杏林製薬株式会社 N−置換ジオキソチアゾリジルベンズアミド誘導体及びその製造法
AU2231397A (en) * 1996-03-08 1997-09-22 Torii Pharmaceutical Co., Ltd. Thiazolidine-2,4-dione derivatives
DE19711616A1 (de) 1997-03-20 1998-09-24 Boehringer Mannheim Gmbh Verbessertes Verfahren zur Herstellung von Thiazolidindionen
EP1103552A4 (en) * 1998-08-07 2003-01-15 Takeda Chemical Industries Ltd BENZOTHIEPINE DERIVATIVES, METHOD FOR THEIR PRODUCTION AND THEIR USE
JP4316787B2 (ja) * 2000-01-11 2009-08-19 壽製薬株式会社 エーテル又はアミド誘導体、その製法並びにそれを含有する糖尿病治療剤、
DE10029077A1 (de) 2000-06-13 2001-12-20 Bayer Ag Thiazolylsubstituierte Heterocyclen
WO2002059100A1 (fr) * 2001-01-26 2002-08-01 Shionogi & Co., Ltd. Composes halogene ayant un agonisme envers le recepteur de thrombopoietine
WO2002062775A1 (fr) * 2001-02-02 2002-08-15 Yamanouchi Pharmaceutical Co., Ltd. Dérivé de 2-acylaminothiazole ou son sel
DE10331675A1 (de) 2003-07-14 2005-02-10 Bayer Cropscience Ag Hetarylsubstituierte Pyrazolidindion-Derivate
WO2008051197A2 (en) 2005-09-20 2008-05-02 Mayo Foundation For Medical Education And Research Small-molecule botulinum toxin inhibitors
GB2465890A (en) * 2008-12-05 2010-06-09 Scynexis Inc 2-Arylazole derivatives as antiprotozoal agents
DE102022131780A1 (de) 2022-11-30 2024-06-06 HELLA GmbH & Co. KGaA Induktiver Drehwinkelsensor

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1003445B (zh) * 1984-10-03 1989-03-01 武田药品工业株式会社 噻唑烷二酮衍生物,其制备方法和用途
US4703052A (en) * 1985-05-21 1987-10-27 Pfizer Inc. Hypoglycemic thiazolidinediones
JPH06779B2 (ja) * 1985-06-10 1994-01-05 武田薬品工業株式会社 チアゾリジオン誘導体およびそれを含んでなる医薬組成物

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7026334B1 (en) 1999-07-26 2006-04-11 Shionogi & Co., Ltd. Thiazolidine compounds and pharmaceutical compositions exhibiting thrombopoietin receptor agonism

Also Published As

Publication number Publication date
WO1989008652A1 (en) 1989-09-21
DK108789A (da) 1989-09-09
ES2052907T3 (es) 1994-07-16
HU882181D0 (en) 1991-01-28
FI904413A0 (sv) 1990-09-07
JPH01299289A (ja) 1989-12-04
MY103837A (en) 1993-09-30
EP0389699B1 (en) 1994-05-11
HUT54680A (en) 1991-03-28
KR890014534A (ko) 1989-10-24
JPH0585551B2 (sv) 1993-12-07
AU3107789A (en) 1989-09-14
NO178068C (no) 1996-01-17
CA1328265C (en) 1994-04-05
CN1026234C (zh) 1994-10-19
KR910000734B1 (ko) 1991-02-06
IL89481A (en) 1993-02-21
FI92696C (sv) 1994-12-27
IL89481A0 (en) 1989-09-10
EP0389699A1 (en) 1990-10-03
NO903863L (no) 1990-09-05
CN1036572A (zh) 1989-10-25
PT89922B (pt) 1995-03-01
NZ228247A (en) 1990-05-28
NO178068B (no) 1995-10-09
ES2052906T3 (es) 1994-07-16
NO903863D0 (no) 1990-09-05
HU217432B (hu) 2000-01-28
AU594899B2 (en) 1990-03-15
PT89922A (pt) 1989-11-10
ZA891681B (en) 1990-10-31
ES2052910T3 (es) 1994-07-16
DK108789D0 (da) 1989-03-07

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FG Patent granted

Owner name: PFIZER INC.

MA Patent expired