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PE83999A1 - Azetidinas - Google Patents

Azetidinas

Info

Publication number
PE83999A1
PE83999A1 PE1998000589A PE00058998A PE83999A1 PE 83999 A1 PE83999 A1 PE 83999A1 PE 1998000589 A PE1998000589 A PE 1998000589A PE 00058998 A PE00058998 A PE 00058998A PE 83999 A1 PE83999 A1 PE 83999A1
Authority
PE
Peru
Prior art keywords
alkyl
optionally replaced
halogen
compound
cycloalkyl
Prior art date
Application number
PE1998000589A
Other languages
English (en)
Inventor
Donald Stuart Middleton
David Alker
Graham Nigel Maw
Thomas Victor Magee
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 PE83999A1 publication Critical patent/PE83999A1/es

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
    • C07D401/02Heterocyclic 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 two hetero rings
    • C07D401/06Heterocyclic 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 two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
    • 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00Drugs for disorders of the urinary system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/04Antibacterial agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12Antivirals
    • 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
    • C07D205/00Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom
    • C07D205/02Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings
    • C07D205/04Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D211/00Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
    • C07D211/04Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D211/06Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
    • C07D211/08Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms
    • C07D211/18Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms
    • C07D211/20Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms with hydrocarbon radicals, substituted by singly bound oxygen or sulphur atoms
    • C07D211/22Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms with hydrocarbon radicals, substituted by singly bound oxygen or sulphur atoms by oxygen atoms
    • 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
    • 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
    • C07D403/04Heterocyclic 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 directly linked by a ring-member-to-ring-member bond

Landscapes

  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Pharmacology & Pharmacy (AREA)
  • General Chemical & Material Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Communicable Diseases (AREA)
  • Pulmonology (AREA)
  • Oncology (AREA)
  • Pain & Pain Management (AREA)
  • Immunology (AREA)
  • Virology (AREA)
  • Rheumatology (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Dermatology (AREA)
  • Urology & Nephrology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)

Abstract

SE REFIERE A UN COMPUESTO DERIVADO DE AZETIDINILPROPILPIPERIDINA DE FORMULA (I), DONDE A ES CO, SO2 o CH2; Ar1 ES FENILO OPCIONALMENTE SUSTITUIDO POR HALOGENO, ALCOXI C1-C6, ALQUILO C1-C6 OPCIONALMENTE SUSTITUIDOS POR HALOGENOS; X1 ES CICLOALQUILO C3-C7 OPCIONALMENTE SUSTITUIDO POR ALQUILO C1-C4, CICLOALQUILO C3-C7, ALCOXILO C1-C4; ARILO O ALQUILO C1-C6 OPCIONALMENTE SUSTITUIDO POR FLUOR, COOH, CO2(ALQUILO C1-C4), ENTRE OTROS; X ES UN ENLACE DIRECTO O NR1; R ES SO2-ARILO, SO2(ALQUILO C1-C6 OPCIONALMENTE SUSTITUIDO POR HALOGENO); R1 ES H, ALQUILO C1-C6 FENILO, OPCIONALMENTE SUSTITUIDO POR HALOGENO; Y ES O, NCO(ALQUILO C1-C6), NCO2(ALQUILO C1-C6) OPCIONALMENTE SUSTITUIDOS POR HALOGENO, ENTRE OTROS; CUANDO R ES UN GRUPO DE FORMULA (a, b), X NO ES NR1. UN COMPUESTO PREFERIDO ES (+)-3-(R)-1-BENZOIL-3-(3-[3-(4-TERC-BUTOXICARBONILPIPERAZIN-1-IL)AZETIDIN-1-IL]PROPIL)-3-(3,4-DICLOROFENILO)PIPERIDINA; ENTRE OTROS. TAMBIEN SE REFIERE A UN PROCEDIMIENTO PARA LA PREPARACION. EL COMPUESTO I ES UN ANTAGONISTA SOBRE UNA TAQUIQUININA QUE ACTUA EN EL RECEPTOR HUMANO NK1, NK2 o NK3; PUDIENDO SER UTIL PARA EL TRATAMIENTO DE UNA ENFERMEDAD INFLAMATORIA COMO ARTRITIS, PSORIASIS, ASMA O ENFERMEDAD INFLAMATORIA DEL INTESTINO
PE1998000589A 1997-07-04 1998-07-01 Azetidinas PE83999A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GBGB9714129.5A GB9714129D0 (en) 1997-07-04 1997-07-04 Azetidines

Publications (1)

Publication Number Publication Date
PE83999A1 true PE83999A1 (es) 1999-09-11

Family

ID=10815370

Family Applications (1)

Application Number Title Priority Date Filing Date
PE1998000589A PE83999A1 (es) 1997-07-04 1998-07-01 Azetidinas

Country Status (36)

Country Link
US (1) US6262046B1 (es)
EP (1) EP1023285A1 (es)
JP (1) JP2000511207A (es)
KR (1) KR20010015532A (es)
CN (1) CN1261887A (es)
AP (1) AP1110A (es)
AR (1) AR013171A1 (es)
AU (1) AU726708B2 (es)
BG (1) BG103992A (es)
BR (1) BR9810544A (es)
CA (1) CA2294193A1 (es)
CO (1) CO4950604A1 (es)
DZ (1) DZ2550A1 (es)
EA (1) EA002773B1 (es)
GB (1) GB9714129D0 (es)
GT (1) GT199800106A (es)
HN (1) HN1998003689A (es)
HR (1) HRP20000002B1 (es)
HU (1) HUP0002330A3 (es)
ID (1) ID24090A (es)
IL (1) IL133433A0 (es)
IS (1) IS5295A (es)
MA (1) MA26519A1 (es)
NO (1) NO996115L (es)
NZ (1) NZ501715A (es)
OA (1) OA11236A (es)
PA (1) PA8454601A1 (es)
PE (1) PE83999A1 (es)
PL (1) PL338004A1 (es)
SK (1) SK182799A3 (es)
TN (1) TNSN98127A1 (es)
TR (1) TR200000025T2 (es)
TW (1) TW492960B (es)
UY (1) UY25079A1 (es)
WO (1) WO1999001451A1 (es)
ZA (1) ZA985875B (es)

Families Citing this family (24)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB9714129D0 (en) 1997-07-04 1997-09-10 Pfizer Ltd Azetidines
WO1999019297A1 (en) * 1997-10-15 1999-04-22 Coelacanth Chemical Corporation Synthesis of azetidine derivatives
FR2787449B3 (fr) 1998-12-15 2001-01-12 Sanofi Sa Derives de 3-phenyl-2,6-dioxopiperidin-3-yl propionamide et leur procede de preparation
FR2787448B3 (fr) 1998-12-18 2001-01-12 Sanofi Sa Ester d'alkyle inferieur de l'acide 3-(3,4-dihalogenophenyl) -2,6-dioxopiperidine3-propionique et son mode de preparation
FR2805810B1 (fr) * 2000-03-03 2002-04-26 Aventis Pharma Sa Compositions pharmaceutiques contenant des derives de 3- amino-azetidine, les nouveaux derives et leur preparation
FR2805817B1 (fr) * 2000-03-03 2002-04-26 Aventis Pharma Sa Compositions pharmaceutiques contenant des derives d'azetidine, les nouveaux derives d'azetidine et leur preparation
US6566356B2 (en) 2000-03-03 2003-05-20 Aventis Pharma S.A. Pharmaceutical compositions containing 3-aminoazetidine derivatives, novel derivatives and their preparation
JP4660199B2 (ja) * 2002-12-23 2011-03-30 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 置換1−ピペリジン−4−イル−4−アゼチジン−3−イル−ピペラジン誘導体およびそれらのニューロキニン拮抗薬としての使用
TW200508221A (en) 2003-06-13 2005-03-01 Astrazeneca Ab New azetidine compounds
TW200630337A (en) * 2004-10-14 2006-09-01 Euro Celtique Sa Piperidinyl compounds and the use thereof
FR2876689B1 (fr) * 2004-10-14 2008-02-22 Aventis Pharma Sa Nouveau procede et intermediaires de preparation de derives de n-(1-benzhydryl-azetidin-3-yl)-n-phenyl-methylsulfonamide
NZ556628A (en) * 2005-03-08 2009-09-25 Janssen Pharmaceutica Nv Diaza-spiro-[4.4]-nonane derivatives as neurokinin (NK1) antagonists
WO2007110449A1 (en) * 2006-03-29 2007-10-04 Euro-Celtique S.A. Benzenesulfonamide compounds and their use
US8791264B2 (en) 2006-04-13 2014-07-29 Purdue Pharma L.P. Benzenesulfonamide compounds and their use as blockers of calcium channels
TW200812963A (en) 2006-04-13 2008-03-16 Euro Celtique Sa Benzenesulfonamide compounds and the use thereof
US8106208B2 (en) 2006-05-18 2012-01-31 Albireo Ab Benzamide compounds that act as NK receptor antagonists
WO2008090114A1 (en) 2007-01-24 2008-07-31 Glaxo Group Limited Pharmaceutical compositions comprising 2-methoxy-5- (5-trifluoromethyl-tetrazol-i-yl-benzyl) - (2s-phenyl-piperidin-3s-yl-)
WO2008124118A1 (en) 2007-04-09 2008-10-16 Purdue Pharma L.P. Benzenesulfonyl compounds and the use therof
ATE517100T1 (de) 2007-08-07 2011-08-15 Hoffmann La Roche Pyrrolidinarylether als nk3-rezeptorantagonisten
US8765736B2 (en) * 2007-09-28 2014-07-01 Purdue Pharma L.P. Benzenesulfonamide compounds and the use thereof
EP3311841B1 (en) 2015-06-16 2021-07-28 PRISM BioLab Co., Ltd. Anticancer agent
CN107614504B (zh) 2015-06-23 2019-12-24 卫材R&D管理有限公司 甲酰胺化合物的晶体
RU2750539C2 (ru) 2017-02-08 2021-06-29 Эйсай Ар Энд Ди Менеджмент Ко., Лтд. Фармацевтическая композиция для лечения опухоли
AU2018269996A1 (en) 2017-05-16 2019-11-21 Eisai R&D Management Co., Ltd. Treatment of hepatocellular carcinoma

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2676055B1 (fr) * 1991-05-03 1993-09-03 Sanofi Elf Composes polycycliques amines et leurs enantiomeres, procede pour leur preparation et compositions pharmaceutiques les contenant.
US5625060A (en) 1991-05-03 1997-04-29 Elf Sanofi Polycyclic amine compounds and their enantiomers, their method of preparation and pharmaceutical compositions on which they are present
TW432061B (en) 1994-08-09 2001-05-01 Pfizer Res & Dev Lactams
FR2729951B1 (fr) * 1995-01-30 1997-04-18 Sanofi Sa Nouveaux composes heterocycliques, procede pour leur preparation et compositions pharmaceutiques en contenant
GB9600235D0 (en) 1996-01-05 1996-03-06 Pfizer Ltd Therapeutic agents
GB9601697D0 (en) * 1996-01-27 1996-03-27 Pfizer Ltd Therapeutic agents
GB9714129D0 (en) 1997-07-04 1997-09-10 Pfizer Ltd Azetidines

Also Published As

Publication number Publication date
GT199800106A (es) 2000-01-05
HN1998003689A (es) 1999-01-08
DZ2550A1 (fr) 2003-02-08
UY25079A1 (es) 2000-12-29
CN1261887A (zh) 2000-08-02
BG103992A (en) 2000-07-31
KR20010015532A (ko) 2001-02-26
IL133433A0 (en) 2001-04-30
AP9801291A0 (en) 1998-09-30
NO996115D0 (no) 1999-12-10
ID24090A (id) 2000-07-06
TR200000025T2 (tr) 2000-06-21
US6262046B1 (en) 2001-07-17
CO4950604A1 (es) 2000-09-01
TW492960B (en) 2002-07-01
GB9714129D0 (en) 1997-09-10
JP2000511207A (ja) 2000-08-29
AR013171A1 (es) 2000-12-13
WO1999001451A1 (en) 1999-01-14
HUP0002330A3 (en) 2002-05-28
OA11236A (en) 2003-05-27
HRP20000002A2 (en) 2000-12-31
BR9810544A (pt) 2000-09-05
EP1023285A1 (en) 2000-08-02
TNSN98127A1 (fr) 2005-03-15
EA002773B1 (ru) 2002-08-29
HRP20000002B1 (en) 2002-06-30
PA8454601A1 (es) 2000-05-24
AP1110A (en) 2002-10-10
EA199901102A1 (ru) 2000-08-28
IS5295A (is) 1999-12-10
NO996115L (no) 2000-02-22
HUP0002330A2 (hu) 2001-06-28
AU8806298A (en) 1999-01-25
NZ501715A (en) 2001-06-29
SK182799A3 (en) 2001-11-06
MA26519A1 (fr) 2004-12-20
PL338004A1 (en) 2000-09-25
AU726708B2 (en) 2000-11-16
CA2294193A1 (en) 1999-01-14
ZA985875B (en) 2000-01-10

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FD Application declared void or lapsed