AR122779A1 - Derivados de tetrazol como inhibidores de trpa1 - Google Patents

Derivados de tetrazol como inhibidores de trpa1

Info

Publication number
AR122779A1
AR122779A1 ARP210101795A ARP210101795A AR122779A1 AR 122779 A1 AR122779 A1 AR 122779A1 AR P210101795 A ARP210101795 A AR P210101795A AR P210101795 A ARP210101795 A AR P210101795A AR 122779 A1 AR122779 A1 AR 122779A1
Authority
AR
Argentina
Prior art keywords
alkyl
group
fluoroalkyl
cycloalkyl
morpholinyl
Prior art date
Application number
ARP210101795A
Other languages
English (en)
Inventor
Florian Paul Christian Binder
Martin Thomas Fleck
Jens Willwacher
Original Assignee
Boehringer Ingelheim Int
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 Boehringer Ingelheim Int filed Critical Boehringer Ingelheim Int
Publication of AR122779A1 publication Critical patent/AR122779A1/es

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Classifications

    • 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
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/513Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim having oxo groups directly attached to the heterocyclic ring, e.g. cytosine
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/535Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
    • A61K31/53751,4-Oxazines, e.g. morpholine
    • A61K31/53771,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • A61P11/14Antitussive 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
    • 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
    • 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
    • C07D403/14Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/14Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D409/00Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/14Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/14Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Engineering & Computer Science (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Pulmonology (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)

Abstract

Derivados de tetrazol que son inhibidores de potencial de receptor transitorio anquirina 1 (TRPA1) y que son útiles para el tratamiento de las enfermedades que se pueden tratar mediante inhibición de TRPA1. Asimismo, composiciones farmacéuticas que lo contienen, y procesos para la preparación de dichos compuestos. Reivindicación 1: Un compuesto caracterizado por la fórmula (1) en donde A se selecciona del grupo que consiste en fenilo, tiofenilo, benzotiofenilo o benzofuranilo, sustituidos o no sustituidos con uno, dos o tres miembros del grupo R³ que consiste en halógeno, C₁₋₄-alquilo, C₁₋₄-fluoroalquilo, C₃₋₄-cicloalquilo, C₃₋₄-ciclofluoroalquilo, O-C₁₋₄-alquilo, O-ciclopropilo y NC-; o A se selecciona del grupo que consiste en los compuestos del grupo de fórmula (2); R¹ se selecciona del grupo que consiste en C₁₋₄-alquilo, C₁₋₄-fluoroalquilo, C₃₋₆-cicloalquilo, R⁴-(H₂C)ₘ- y R⁵-(H₂C)ₙ-; en donde m es 1 ó 2; n es 2; R⁴ es C₃₋₆-cicloalquilo; R⁵ es -O-C₁₋₄-alquilo o -O-C₁₋₄-fluoroalquilo; R² se selecciona del grupo que consiste en H, C₁₋₄-alquilo, C₃₋₆-cicloalquilo, C₃₋₆-ciclofluoroalquilo, HO-C₁₋₄-alquilo-, C₁₋₄-fluoroalquilo, R⁶-(H₂C)ₚ-, R⁷-(H₂C)q-, R⁶-(H(R⁸)C)ₚ- y R⁷-(H(R⁹)C)q-; en donde p es 1 ó 2; q es 2; R⁶ se selecciona del grupo que consiste en HO-C₁₋₂-alquilo-, C₃₋₆-cicloalquilo, C-morfolinilo, C-imidazolilo y C-pirazolilo; en donde dichos C-pirazolilo, C-imidazolilo y C-morfolinilo no se sustituyen o se sustituyen con C₁₋₄-alquilo o C₁₋₄-fluoroalquilo; R⁷ se selecciona del grupo que consiste en C₁₋₄-alquil-O-, C₁₋₄-fluoroalquil-O-, C₁₋₄-alquil-S(O)₂-, N-morfolinilo, N-imidazolilo y N-pirazolilo; en donde dichos N-pirazolilo, N-imidazolilo, N-morfolinilo no se sustituyen o se sustituyen con C₁₋₄-alquilo o C₁₋₄-fluoroalquilo; R⁸ y R⁹ se seleccionan independientemente de H o C₁₋₄-alquilo.
ARP210101795A 2020-06-29 2021-06-28 Derivados de tetrazol como inhibidores de trpa1 AR122779A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
EP20182988 2020-06-29

Publications (1)

Publication Number Publication Date
AR122779A1 true AR122779A1 (es) 2022-10-05

Family

ID=71401656

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP210101795A AR122779A1 (es) 2020-06-29 2021-06-28 Derivados de tetrazol como inhibidores de trpa1

Country Status (19)

Country Link
US (1) US11884652B2 (es)
EP (1) EP4171563A1 (es)
JP (1) JP7539501B2 (es)
KR (1) KR20230028547A (es)
CN (1) CN115803029A (es)
AR (1) AR122779A1 (es)
AU (1) AU2021298800A1 (es)
BR (1) BR112022021865A2 (es)
CA (1) CA3181350A1 (es)
CL (1) CL2022003329A1 (es)
CO (1) CO2022016755A2 (es)
CR (1) CR20220667A (es)
DO (1) DOP2022000262A (es)
EC (1) ECSP22088664A (es)
IL (1) IL299175A (es)
MX (1) MX2022016357A (es)
SA (1) SA522441965B1 (es)
TW (1) TW202216688A (es)
WO (1) WO2022002782A1 (es)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US11858921B2 (en) 2021-04-14 2024-01-02 Boehringer Ingelheim International Gmbh Uracil derivatives as TRPA1 inhibitors
MX2024009581A (es) * 2022-02-03 2024-08-13 D E Shaw Res Llc Compuestos de uracilo n3-sustituidos como inhibidores de trpa1.

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7361654B2 (en) 2005-01-13 2008-04-22 Bristol-Myers Squibb Co. Substituted heteroaryl amide modulators of glucocorticoid receptor, AP-1, and/or NF-κB activity and use thereof
JP2011231015A (ja) 2008-08-29 2011-11-17 Taiho Yakuhin Kogyo Kk 含窒素複素環を有する新規ウラシル化合物又はその塩
WO2017060488A1 (en) 2015-10-09 2017-04-13 Almirall, S.A. New trpa1 antagonists
EP3544979B1 (en) * 2016-11-28 2021-08-04 F. Hoffmann-La Roche AG Oxadiazolones as transient receptor potential channel inhibitors
US11858921B2 (en) 2021-04-14 2024-01-02 Boehringer Ingelheim International Gmbh Uracil derivatives as TRPA1 inhibitors

Also Published As

Publication number Publication date
DOP2022000262A (es) 2023-01-31
CL2022003329A1 (es) 2023-03-31
US11884652B2 (en) 2024-01-30
US20220002270A1 (en) 2022-01-06
CN115803029A (zh) 2023-03-14
BR112022021865A2 (pt) 2023-01-24
ECSP22088664A (es) 2022-12-30
TW202216688A (zh) 2022-05-01
CA3181350A1 (en) 2022-01-06
CO2022016755A2 (es) 2022-11-29
WO2022002782A1 (en) 2022-01-06
IL299175A (en) 2023-02-01
JP7539501B2 (ja) 2024-08-23
CR20220667A (es) 2023-02-03
SA522441965B1 (ar) 2024-07-21
MX2022016357A (es) 2023-01-24
EP4171563A1 (en) 2023-05-03
AU2021298800A1 (en) 2022-11-24
JP2023531924A (ja) 2023-07-26
KR20230028547A (ko) 2023-02-28

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