PE20212199A1 - Sintesis de 4-amino-5-metil-1h-piridin-2(1h)-on (compuesto intermedio para la sintesis del antagonista finerenona de mr) a partir de 2-cloro-5-metil-4-nitro-piridina-1-oxido usando el compuesto intermedio 2-cloro-5-metil-4-piridinamina - Google Patents

Sintesis de 4-amino-5-metil-1h-piridin-2(1h)-on (compuesto intermedio para la sintesis del antagonista finerenona de mr) a partir de 2-cloro-5-metil-4-nitro-piridina-1-oxido usando el compuesto intermedio 2-cloro-5-metil-4-piridinamina

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Publication number
PE20212199A1
PE20212199A1 PE2021001422A PE2021001422A PE20212199A1 PE 20212199 A1 PE20212199 A1 PE 20212199A1 PE 2021001422 A PE2021001422 A PE 2021001422A PE 2021001422 A PE2021001422 A PE 2021001422A PE 20212199 A1 PE20212199 A1 PE 20212199A1
Authority
PE
Peru
Prior art keywords
methyl
chloro
synthesis
intermediate compound
amino
Prior art date
Application number
PE2021001422A
Other languages
English (en)
Inventor
Johannes Platzek
Kai Lovis
Original Assignee
Bayer Ag
Bayer Pharma 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
Application filed by Bayer Ag, Bayer Pharma AG filed Critical Bayer Ag
Publication of PE20212199A1 publication Critical patent/PE20212199A1/es

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Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D213/00Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom 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
    • C07D213/72Nitrogen atoms
    • C07D213/73Unsubstituted amino or imino radicals
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pyridine Compounds (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

Abstract

SE REFIERE A UN PROCEDIMIENTO PARA LA PREPARACION DEL INTERMEDIO 4-AMINO-5-METILPIRIDONA DE FORMULA (I) QUE COMPRENDE HACER REACCIONAR EL COMPUESTO 2-CLORO-5-METILPIRIDIN-4-AMINO DE FORMULA (2) EN AUTOCLAVE CON KOH EN PRESENCIA DE METANOL A UNA TEMPERATURA EN EL RANGO DE 160 °C A 200 °C. DICHO COMPUESTO DE FORMULA (I) ES UN INTERMEDIO PARA LA PREPARACION DE FINERENONA QUE ES UN ANTAGONISTA NO ESTEROIDE DEL RECEPTOR MINERALOCORTICOIDE QUE ES UTIL EN EL TRATAMIENTO DE INSUFICIENCIA CARDIACA Y NEFROPATIA DIABETICA.
PE2021001422A 2019-03-05 2020-02-28 Sintesis de 4-amino-5-metil-1h-piridin-2(1h)-on (compuesto intermedio para la sintesis del antagonista finerenona de mr) a partir de 2-cloro-5-metil-4-nitro-piridina-1-oxido usando el compuesto intermedio 2-cloro-5-metil-4-piridinamina PE20212199A1 (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP19160904 2019-03-05
PCT/EP2020/055292 WO2020178175A1 (de) 2019-03-05 2020-02-28 Synthese von 4-amino-5-methyl-1h-pyridin-2(1h)-on (zwischenverbindung der synthese des mr antagonisten finerenone) aus 2-chloro-5-methyl-4-nitro-pyridine-1-oxid über die zwischenverbindung 2-chloro-5-methyl-4-pyridinamin

Publications (1)

Publication Number Publication Date
PE20212199A1 true PE20212199A1 (es) 2021-11-16

Family

ID=65991501

Family Applications (1)

Application Number Title Priority Date Filing Date
PE2021001422A PE20212199A1 (es) 2019-03-05 2020-02-28 Sintesis de 4-amino-5-metil-1h-piridin-2(1h)-on (compuesto intermedio para la sintesis del antagonista finerenona de mr) a partir de 2-cloro-5-metil-4-nitro-piridina-1-oxido usando el compuesto intermedio 2-cloro-5-metil-4-piridinamina

Country Status (16)

Country Link
US (1) US20220153699A1 (es)
EP (1) EP3935045A1 (es)
JP (1) JP2022523986A (es)
KR (1) KR20210135238A (es)
CN (1) CN113474332A (es)
AU (1) AU2020230965A1 (es)
BR (1) BR112021014815A2 (es)
CA (1) CA3132399A1 (es)
CL (1) CL2021002316A1 (es)
CO (1) CO2021011553A2 (es)
IL (1) IL285937A (es)
JO (1) JOP20210242A1 (es)
MX (1) MX2021010612A (es)
PE (1) PE20212199A1 (es)
SG (1) SG11202109546RA (es)
WO (1) WO2020178175A1 (es)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN114656400A (zh) * 2022-04-26 2022-06-24 浙江科聚生物医药有限公司 一种非奈利酮关键中间体的制备方法

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1311185A (zh) * 2000-03-03 2001-09-05 山东新华制药股份有限公司 4-氨基吡啶及衍生物的制备方法
US7462612B2 (en) 2004-03-26 2008-12-09 Vertex Pharmaceuticals Incorporated Pyridine inhibitors of ERK2 and uses thereof
DE102007009494A1 (de) 2007-02-27 2008-08-28 Bayer Healthcare Ag Substituierte 4-Aryl-1, 4-dihydro-1,6-naphthyridinamide und ihre Verwendung
CN103193704B (zh) * 2013-04-12 2016-03-09 四川铂瑞生物医药有限公司 2-羟基-4-氨基-5-甲基吡啶杂环化合物
HUE051350T2 (hu) 2014-08-01 2021-03-01 Bayer Pharma AG Eljárás (4S)-4-(4-ciano-2-metoxifenil)-5-etoxi-2,8-dimetil-1,4-dihidro-1,6-naftridin-3-karboxamid elõállítására és tisztítására gyógyászati hatóanyagként való alkalmazása céljából

Also Published As

Publication number Publication date
AU2020230965A1 (en) 2021-09-23
WO2020178175A1 (de) 2020-09-10
CL2021002316A1 (es) 2022-04-08
CO2021011553A2 (es) 2021-09-20
IL285937A (en) 2021-10-31
EP3935045A1 (de) 2022-01-12
JP2022523986A (ja) 2022-04-27
SG11202109546RA (en) 2021-09-29
JOP20210242A1 (ar) 2023-01-30
CA3132399A1 (en) 2020-09-10
BR112021014815A2 (pt) 2021-09-28
CN113474332A (zh) 2021-10-01
MX2021010612A (es) 2021-09-28
US20220153699A1 (en) 2022-05-19
KR20210135238A (ko) 2021-11-12

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