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CO5640113A2 - Amidas de acido pieprazinil o piepridinilamin-sulfamico como inhibidores de la sulfatasa esteroidal - Google Patents

Amidas de acido pieprazinil o piepridinilamin-sulfamico como inhibidores de la sulfatasa esteroidal

Info

Publication number
CO5640113A2
CO5640113A2 CO04096497A CO04096497A CO5640113A2 CO 5640113 A2 CO5640113 A2 CO 5640113A2 CO 04096497 A CO04096497 A CO 04096497A CO 04096497 A CO04096497 A CO 04096497A CO 5640113 A2 CO5640113 A2 CO 5640113A2
Authority
CO
Colombia
Prior art keywords
carbon atoms
aryl
r4ss
r3ss
aminocarbonyl
Prior art date
Application number
CO04096497A
Other languages
English (en)
Inventor
Philipp Lehr
Original Assignee
Novartis Ag
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
Priority claimed from GB0207500A external-priority patent/GB0207500D0/en
Priority claimed from GB0225679A external-priority patent/GB0225679D0/en
Application filed by Novartis Ag filed Critical Novartis Ag
Publication of CO5640113A2 publication Critical patent/CO5640113A2/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D295/00Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
    • C07D295/22Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with hetero atoms directly attached to ring nitrogen atoms
    • C07D295/26Sulfur atoms
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • A61P17/02Drugs for dermatological disorders for treating wounds, ulcers, burns, scars, keloids, or the like
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • A61P17/08Antiseborrheics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • A61P17/10Anti-acne agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • A61P17/14Drugs for dermatological disorders for baldness or alopecia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/28Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • 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
    • C07D211/36Heterocyclic 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 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
    • C07D211/56Nitrogen atoms
    • C07D211/58Nitrogen atoms attached in position 4

Landscapes

  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Dermatology (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Hospice & Palliative Care (AREA)
  • Psychiatry (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Hydrogenated Pyridines (AREA)

Abstract

1.- Un compuesto de la fórmula:en donde cualquiera de: - R1 y R2, junto con el átomo de nitrógeno con el que están unidos, son piperazinilo, en donde el segundo átomo de nitrógeno está sustituido por alcoxilo(de 1 a 6 átomos de carbono) -carbonilo, o por arilo (de 6 a 18 átomos de carbono), cuyo arilo (de 6 a 18 átomos de carbono) está sustituido por uno o más de halógeno, haloalquilo (de 1 a 6 átomos de carbono), por ejemplo CF3, ó aminocarbonilo;ó - R1 es hidrógeno y R2 es piperidinilo, unido por medio de un átomo de carbono del anillo de piperidinilo, en donde el átomo de nitrógeno está sustituido por alcoxilo(de 1 a 6 átomos de carbono)-carbonilo, o por arilo (de 6 a 18 átomos de carbono), y R3 es arilo (de 6 a 18 átomos de carbono) ó arilo (de 6 a 18 átomos de carbono) -alquilo (de 1 a 4 átomos de carbono), cuyo arilo está sustituido por uno o más de halógeno, aminocarbonilo, ó haloalquilo (de 1 a 6 átomos de carbono).2.- Un compuesto de la reivindicación 1, seleccionado a partir del grupo que consiste en los compuestos de la fórmula:en donde: a. R3ss es 3, 5-bis (trifluorometil) fenilo, y R4ss es 2-aminocarbonil-5-trifluorometilfenilo, b. R3ss es 2,3-diclorofenilo, R4ss es 2-aminocarbonil-5-trifluorometilfenilo, c. R3ss es 3,5-diclorofenilo, R4ss es 2-amino-carbonil-5-trifluorometilfenilo, y d. R3ss es 3,5-bis(trifluorometil)fenilo, y R4ss es terbutoxicarbonilo.
CO04096497A 2002-03-28 2004-09-28 Amidas de acido pieprazinil o piepridinilamin-sulfamico como inhibidores de la sulfatasa esteroidal CO5640113A2 (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GB0207500A GB0207500D0 (en) 2002-03-28 2002-03-28 Organic compounds
GB0225679A GB0225679D0 (en) 2002-11-04 2002-11-04 Organic compounds

Publications (1)

Publication Number Publication Date
CO5640113A2 true CO5640113A2 (es) 2006-05-31

Family

ID=28676499

Family Applications (1)

Application Number Title Priority Date Filing Date
CO04096497A CO5640113A2 (es) 2002-03-28 2004-09-28 Amidas de acido pieprazinil o piepridinilamin-sulfamico como inhibidores de la sulfatasa esteroidal

Country Status (20)

Country Link
US (2) US7439362B2 (es)
EP (1) EP1492782A1 (es)
JP (1) JP4580652B2 (es)
KR (1) KR20040094877A (es)
CN (1) CN1293065C (es)
AR (1) AR039156A1 (es)
AU (1) AU2003226732B2 (es)
BR (1) BR0308795A (es)
CA (1) CA2480686A1 (es)
CO (1) CO5640113A2 (es)
IL (1) IL164267A0 (es)
MX (1) MXPA04009453A (es)
MY (1) MY136880A (es)
NO (1) NO20044321L (es)
NZ (1) NZ535617A (es)
PE (1) PE20040167A1 (es)
PL (1) PL372602A1 (es)
RU (1) RU2329258C2 (es)
TW (1) TW200306806A (es)
WO (1) WO2003082842A1 (es)

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GB0505541D0 (en) * 2005-03-17 2005-04-27 Novartis Ag Organic compounds
GB0505539D0 (en) * 2005-03-17 2005-04-27 Novartis Ag Organic compounds
GB0511190D0 (en) * 2005-06-01 2005-07-06 Sterix Ltd Use
WO2009037539A2 (en) 2007-09-17 2009-03-26 Preglem S.A. Treatment of oestrogen dependant conditions in pre-menopausal women
WO2017137423A1 (en) 2016-02-08 2017-08-17 Synaffix B.V. Improved sulfamide linkers for use in bioconjugates
WO2017137456A1 (en) * 2016-02-08 2017-08-17 Synaffix B.V. Bioconjugates containing sulfamide linkers for use in treatment
US11590239B2 (en) 2016-02-08 2023-02-28 Synaffix B.V. Antibody-conjugates with improved therapeutic index for targeting CD30 tumours and method for improving therapeutic index of antibody-conjugates
US20220267260A1 (en) * 2016-11-29 2022-08-25 Epizyme, Inc. Compounds containing a sulfonic group as kat inhibitors
EP3983388A1 (en) * 2019-06-12 2022-04-20 Nodthera Limited Sulfonamide derivatives and uses thereof
CN110590896B (zh) * 2019-11-04 2022-08-30 上海高准医药有限公司 雌酚酮硫酸酯哌嗪的制备方法

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Also Published As

Publication number Publication date
JP4580652B2 (ja) 2010-11-17
CA2480686A1 (en) 2003-10-09
PE20040167A1 (es) 2004-05-26
MY136880A (en) 2008-11-28
BR0308795A (pt) 2005-01-18
CN1293065C (zh) 2007-01-03
NZ535617A (en) 2006-04-28
RU2329258C2 (ru) 2008-07-20
EP1492782A1 (en) 2005-01-05
PL372602A1 (en) 2005-07-25
AU2003226732B2 (en) 2006-12-21
US20060052393A1 (en) 2006-03-09
NO20044321L (no) 2004-10-12
US7439362B2 (en) 2008-10-21
KR20040094877A (ko) 2004-11-10
WO2003082842A1 (en) 2003-10-09
MXPA04009453A (es) 2005-01-25
AR039156A1 (es) 2005-02-09
IL164267A0 (en) 2005-12-18
TW200306806A (en) 2003-12-01
RU2004131822A (ru) 2005-07-10
JP2005526812A (ja) 2005-09-08
CN1646509A (zh) 2005-07-27
US20090042899A1 (en) 2009-02-12
AU2003226732A1 (en) 2003-10-13

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