PE20220842A1 - Metodos sinteticos mejorados para la elaboracion de compuestos de (2h-1,2,3-triazol-2-il)fenilo como moduladores del receptor de orexina - Google Patents

Metodos sinteticos mejorados para la elaboracion de compuestos de (2h-1,2,3-triazol-2-il)fenilo como moduladores del receptor de orexina

Info

Publication number
PE20220842A1
PE20220842A1 PE2022000208A PE2022000208A PE20220842A1 PE 20220842 A1 PE20220842 A1 PE 20220842A1 PE 2022000208 A PE2022000208 A PE 2022000208A PE 2022000208 A PE2022000208 A PE 2022000208A PE 20220842 A1 PE20220842 A1 PE 20220842A1
Authority
PE
Peru
Prior art keywords
triazol
elaboration
orexin receptor
synthetic methods
receptor modulators
Prior art date
Application number
PE2022000208A
Other languages
English (en)
Inventor
Dominique Paul M Depre
Kiran Matcha
Florian Damien Medina
Pieter Westerduin
Cheng Yi Chen
Original Assignee
Janssen Pharmaceutica Nv
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 Janssen Pharmaceutica Nv filed Critical Janssen Pharmaceutica Nv
Publication of PE20220842A1 publication Critical patent/PE20220842A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04Ortho-condensed systems
    • 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
    • A61K31/506Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/20Hypnotics; Sedatives
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/24Antidepressants
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C249/00Preparation of compounds containing nitrogen atoms doubly-bound to a carbon skeleton
    • C07C249/16Preparation of compounds containing nitrogen atoms doubly-bound to a carbon skeleton of hydrazones
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C251/00Compounds containing nitrogen atoms doubly-bound to a carbon skeleton
    • C07C251/72Hydrazones
    • C07C251/74Hydrazones having doubly-bound carbon atoms of hydrazone groups bound to hydrogen atoms or to acyclic carbon atoms
    • C07C251/76Hydrazones having doubly-bound carbon atoms of hydrazone groups bound to hydrogen atoms or to acyclic carbon atoms to carbon atoms of a saturated carbon skeleton
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C251/00Compounds containing nitrogen atoms doubly-bound to a carbon skeleton
    • C07C251/72Hydrazones
    • C07C251/74Hydrazones having doubly-bound carbon atoms of hydrazone groups bound to hydrogen atoms or to acyclic carbon atoms
    • C07C251/78Hydrazones having doubly-bound carbon atoms of hydrazone groups bound to hydrogen atoms or to acyclic carbon atoms to carbon atoms of an unsaturated carbon skeleton
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C311/00Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
    • C07C311/48Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups having nitrogen atoms of sulfonamide groups further bound to another hetero atom
    • C07C311/49Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups having nitrogen atoms of sulfonamide groups further bound to another hetero atom to nitrogen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D249/00Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
    • C07D249/02Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
    • C07D249/041,2,3-Triazoles; Hydrogenated 1,2,3-triazoles
    • C07D249/061,2,3-Triazoles; Hydrogenated 1,2,3-triazoles with aryl radicals directly attached to ring atoms
    • 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
    • C07D295/28Nitrogen atoms
    • C07D295/30Nitrogen atoms non-acylated

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Neurosurgery (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Epidemiology (AREA)
  • Pain & Pain Management (AREA)
  • Psychiatry (AREA)
  • Anesthesiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)

Abstract

SE REFIERE A UN PROCESO PARA PREPARAR EL COMPUESTO ((3aR,6aS)-5-(4,6-DIMETILPIRIMIDIN-2-IL)HEXAHIDROPIRROLO[3,4-C]PIRROL-2(1H)-IL)(2-FLUORO-6-(2H-1,2,3-TRIAZOL-2-IL)FENIL)METANONA (SELTOREXANT), EL CUAL COMPRENDE LA CICLIZACION DE LA HIDRAZINA DEL COMPUESTO DE FORMULA (I) PARA OBTENER EL COMPUESTO 2-FENIL-2H-1,2,3-TRIAZOL DE FORMULA (II) EN UNA SOLA ETAPA, DONDE R1 ES -H, -CO2H O -CO2-ALQUILO(C1-C4); X ES -OH, -OC(O)CH3, -OSO2CH3, -N(CH3)2, ENTRE OTROS. DICHO COMPUESTO SELTOREXANT ES UN MODULADOR DEL RECEPTOR DE OREXINA SIENDO UTIL EN EL TRATAMIENTO DE INSOMNIO Y DEPRESION.
PE2022000208A 2019-08-07 2020-08-06 Metodos sinteticos mejorados para la elaboracion de compuestos de (2h-1,2,3-triazol-2-il)fenilo como moduladores del receptor de orexina PE20220842A1 (es)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201962883857P 2019-08-07 2019-08-07
US202062971265P 2020-02-07 2020-02-07
PCT/EP2020/072192 WO2021023843A1 (en) 2019-08-07 2020-08-06 Improved synthetic methods of making (2h-1,2,3-triazol-2-yl)phenyl compounds as orexin receptor modulators

Publications (1)

Publication Number Publication Date
PE20220842A1 true PE20220842A1 (es) 2022-05-24

Family

ID=72139573

Family Applications (1)

Application Number Title Priority Date Filing Date
PE2022000208A PE20220842A1 (es) 2019-08-07 2020-08-06 Metodos sinteticos mejorados para la elaboracion de compuestos de (2h-1,2,3-triazol-2-il)fenilo como moduladores del receptor de orexina

Country Status (15)

Country Link
US (1) US20220289754A1 (es)
EP (1) EP4010325A1 (es)
JP (1) JP2022543286A (es)
KR (1) KR20220044323A (es)
CN (1) CN114555603A (es)
AU (1) AU2020324552A1 (es)
BR (1) BR112022002128A2 (es)
CA (1) CA3149689A1 (es)
CR (1) CR20220050A (es)
EC (1) ECSP22016630A (es)
IL (1) IL290362A (es)
JO (1) JOP20220031A1 (es)
MX (1) MX2022001615A (es)
PE (1) PE20220842A1 (es)
WO (1) WO2021023843A1 (es)

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4826833A (en) * 1984-01-30 1989-05-02 Pfizer Inc. 6-(Substituted)methylene-penicillanic and 6-(substituted)hydroxymethylpenicillanic acids and derivatives thereof
KR101859400B1 (ko) * 2009-10-23 2018-05-18 얀센 파마슈티카 엔.브이. 오렉신 수용체 조절제로서의 이치환된 옥타하이드로피롤로[3,4-c]피롤
US8299117B2 (en) * 2010-06-16 2012-10-30 Metabolex Inc. GPR120 receptor agonists and uses thereof
EP3125692B1 (en) * 2014-04-01 2021-01-27 Bayer CropScience Aktiengesellschaft Use of heterocyclic compounds for controlling nematodes

Also Published As

Publication number Publication date
US20220289754A1 (en) 2022-09-15
CR20220050A (es) 2022-04-20
IL290362A (en) 2022-04-01
MX2022001615A (es) 2022-05-26
EP4010325A1 (en) 2022-06-15
ECSP22016630A (es) 2022-04-29
WO2021023843A1 (en) 2021-02-11
JP2022543286A (ja) 2022-10-11
AU2020324552A1 (en) 2022-03-24
BR112022002128A2 (pt) 2022-06-07
CA3149689A1 (en) 2021-02-11
CN114555603A (zh) 2022-05-27
JOP20220031A1 (ar) 2023-01-30
KR20220044323A (ko) 2022-04-07

Similar Documents

Publication Publication Date Title
PE20201448A1 (es) Moduladores de enzimas modificadoras de metilo, composiciones y usos de estos
AR063343A1 (es) Compuestos para modular c-kit y receptores de pdgfr
ECSP22015801A (es) Formas sólidas de un inhibidor de hpk1
PE20051051A1 (es) Compuestos de triazol como antagonistas de la vasopresina
CR20120273A (es) OCTAHIDROPIRROLO[3,4-c]PIRROLOS DISUSTITUIDOS COMO MODULADORES DEL RECEPTOR DE OREXINA
PE20081850A1 (es) Derivados ciclizados como inhibidores de la eg-5
PE20090511A1 (es) Imidazopiridinonas
NI200300053A (es) Derivados del tropano utiles en terapia.
PE20121512A1 (es) Novedosos derivados de triazol sustituidos como moduladores de la gamma secretasa
ECSP077994A (es) Aminopirimidinas como moduladores de cinasa
EA201000003A1 (ru) Ингибиторы протеинкиназ и способы их применения
PE20171342A1 (es) Compuestos y su uso como inhibidores de bace
UY32968A (es) Compuestos heterocíclicos fusionados como moduladores del receptor de orexina
MX2020010369A (es) Particulas implantables y metodos relacionados.
EP3037421A3 (en) Mlk inhibitors and methods of use
NI200700316A (es) Aminopirimidinas como moduladores de la cinasa
CL2009000619A1 (es) Compuestos derivados de carbazol, inhibidores de la proteina hsp90; procedimiento para preparar los compuestos; compuestos intermediarios, composicion farmaceutica que comprende a uno de los compuestos; y el uso de los compuestos en el tratamiento del cancer.
PE20070122A1 (es) Proceso para preparar derivados de piperazina azindoloxoacetica sustituida con triazol y nuevas formas de sal producidas de los mismos
PE20110582A1 (es) Arilciclohexileteres de dihidro-tetraazabenzoazuleno
CL2008003063A1 (es) Compuestos derivados de 1,3,4-tiadiazol espiro condensado, inhibidores de la actividad quinesina ksp; composicion farmaceutica; y su uso en el tratamiento de enfermedades proliferativas tales como el cancer, hiperplasia, hipertrofia cardiaca, enfermedades autoinmune, trastornos fungicos, artritis, rechazo a imjertos, entre otras.
PE20212196A1 (es) Compuestos, composiciones, y metodos para modular la actividad cdk9
WO2018053264A3 (en) Klrg1 depletion therapy
PE20221485A1 (es) Macrociclos para uso en el tratamiento de enfermedades
PH12021551054A1 (en) Improved synthetic methods of making fused heterocyclic compounds as orexin receptor modulators
PE20210671A1 (es) Triazolobenzazepinas como antagonistas del receptor v1a de la vasopresina