CO5070713A1 - Procedimiento para la preparacion de acidos hidroxamicos - Google Patents

Procedimiento para la preparacion de acidos hidroxamicos

Info

Publication number
CO5070713A1
CO5070713A1 CO99021089A CO99021089A CO5070713A1 CO 5070713 A1 CO5070713 A1 CO 5070713A1 CO 99021089 A CO99021089 A CO 99021089A CO 99021089 A CO99021089 A CO 99021089A CO 5070713 A1 CO5070713 A1 CO 5070713A1
Authority
CO
Colombia
Prior art keywords
aryl
heteroaryl
alkyl
alkoxy
oxyheteroaryl
Prior art date
Application number
CO99021089A
Other languages
English (en)
Inventor
Joel Michael Hawkins
Original Assignee
Pfizer Prod Inc
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 Prod Inc filed Critical Pfizer Prod Inc
Publication of CO5070713A1 publication Critical patent/CO5070713A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C239/00Compounds containing nitrogen-to-halogen bonds; Hydroxylamino compounds or ethers or esters thereof
    • C07C239/08Hydroxylamino compounds or their ethers or esters
    • C07C239/14Hydroxylamino compounds or their ethers or esters having nitrogen atoms of hydroxylamino groups further bound to carbon atoms of hydrocarbon radicals substituted by doubly-bound oxygen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D493/00Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system
    • C07D493/02Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system in which the condensed system contains two hetero rings
    • C07D493/08Bridged systems
    • 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
    • A61P19/00Drugs for skeletal 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
    • 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
    • A61P9/00Drugs for disorders of the cardiovascular system
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C303/00Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides
    • C07C303/36Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides of amides of sulfonic acids
    • C07C303/40Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides of amides of sulfonic acids by reactions not involving the formation of sulfonamide groups
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D309/00Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings
    • C07D309/02Heterocyclic compounds containing six-membered rings having one oxygen 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
    • C07D309/04Heterocyclic compounds containing six-membered rings having one oxygen 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 with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (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)
  • Public Health (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Pulmonology (AREA)
  • Cardiology (AREA)
  • Rheumatology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Pain & Pain Management (AREA)
  • Immunology (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Pyridine Compounds (AREA)
  • Pyrane Compounds (AREA)

Abstract

Un procedimiento para la preparación de una molécula que contiene un grupo ácido hidroxámico que comprende la reacción de hidroxilamina, o una sal de la misma, con haluro de sililo en presencia de una base, seguido de la reacción con una molécula que contiene un haluro de ácido carboxílico seguido de la reacción con un ácido, con la condición de que la molécula que contiene un haluro de ácido carboxílico no contenga un grupo hidroxi, una amina primaria, una amina secundaria o un grupo tiol.La presente invención se refiere a un procedimiento para la preparación de ácidos hidroxámidos a partir de intermedios ácido hidroxílico, en el que el intermedio de ácido carboxílico no posee sustituyentes eractivos, tales como grupos hidroxi o amino. Un procedimiento para la preparación de un compuesto de fórmula Z es ANDgt;CH2 o ANDgt;NR1 ; Q es alquilo (C1-C6 ), arilo (C6- C10 ), heteroarilo (C2 -C9 ), oxiarilo (C6 -C10 )alquilo (C1 -C6 ), oxiarilo (C6 -C10 )arilo (C6 -C10 )oxiarilo (C6 -C10 ) heteroarilo (C2 -C9 ), arilo (C6 -C10 ), alquilo (C1 -C6 ), aril (C6 -C10 ), arilo (C6 -C10 ), aril (C6 -C10 ), heteroarilo (C2 -C9 ), aril (C6 -C10 ), aril (C6 -C10 ), alquilo (C1 -C6 ).aril (C6-C10) aril (C6-C10) arilo (C1-C10) , aril (C6-C10) aril (C6-C10) heteroarilo (C2-C9), heteroaril (C2-C9) alquilo (C1-C6) , heteroaril (C2-C9) arilo (C6-C10), heteroarilo (C2-C9) heteroarilo (C2-C9), arilo (C6-C10) alcoxi (C1-C6) alquilo (C1- C6) , arilo (C6-C10) alcoxi (C1-C6) arilo (C6-C10) , aril (C6-C10) alcoxi (C1-C6) heteroarilo (C2-C9) , oxiheteroarilo (C2-C9) alquilo (C1-C6) , oxiheteroarilo (C2-C9) arilo (C6-C10), oxiheteroarilo (C2-C9) heteroarilo (C2-C9), heteroaril (C2-C9) alcoxi (C1-C6) alquilo (C1-C6) , heteroaril (C2-C9) alcoxi (C1-C6) arilo (C6-C10) o heteroaril (C2- C9) alcoxi (C1-C6) heteroarilo (C2 - C9); en la que cada radical arilo (C6-C10) o heteroarilo (C2-C9) de dichos arilo (C6-C10), heteroarilo (C2-C9), oxiarilo (C6-C10) alquilo (C1-C6), oxiarilo (C6-C10) arilo (C6-C10), oxiarilo (C6-C10) heteroarilo (C2-C9), arilo (C6-C10) alquilo (C1-C6), aril (C6-C10) arilo (C6-C10) , aril (C6-C10) heteroarilo (C2-C9), aril (C6-C10) aril (C6-C10) alquilo (C1-C6) , aril (C6-C10) aril (C6-C10) arilo (C6-C10), aril (C6-C10) aril (C6-C10) heteroarilo (C2-C9), heteroaril (C2-C9) alquilo (C1-C6), heteroaril (C2-C9) arilo (C6-C10), heteroarilo (C2-C9) heteroarilo (C2-C9), arilo (C6-C10) alcoxi (C1-C6) alquilo (C1-C6), arilo (C6-C10) alcoxi (C1-C6) arilo (C6-C10) , arilo (C6-C10) alcoxi (C1-C6) heteroarilo (C2-C9), oxiheteroarilo (C2-C9) alquilo (C1-C6), oxiheteroarilo (C2-C9) arilo (C6-C10), oxiheterarilo (C2-C9) heteroarilo (C2-C9), heteroaril (C2-C9) alcoxi (C1-C6) alquilo (C1-C6), heteroaril (C2-C9) alcoxi (C1-C6) arilo (C6-C10) o heteroaril (C2-C9) alcoxi (C1-C6) heteroarilo (C2-C9) está opcionalmente sustituido sobre cualquiera de los átomos de carbono del anillo capaces de formar un enlace adicional mediante uno o más sustituyentes por anillo independientemente seleccionado entre fluoro, cloro, bromo, alquilo (C1-C6), alcoxi (C1-C6), ...
CO99021089A 1998-04-10 1999-04-09 Procedimiento para la preparacion de acidos hidroxamicos CO5070713A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US8136598P 1998-04-10 1998-04-10

Publications (1)

Publication Number Publication Date
CO5070713A1 true CO5070713A1 (es) 2001-08-28

Family

ID=22163686

Family Applications (1)

Application Number Title Priority Date Filing Date
CO99021089A CO5070713A1 (es) 1998-04-10 1999-04-09 Procedimiento para la preparacion de acidos hidroxamicos

Country Status (38)

Country Link
US (1) US6288246B1 (es)
EP (1) EP0949244A3 (es)
JP (1) JPH11343277A (es)
KR (1) KR100329902B1 (es)
CN (1) CN1232023A (es)
AP (1) AP1203A (es)
AR (1) AR018180A1 (es)
AU (1) AU747629B2 (es)
BG (1) BG64154B1 (es)
BR (1) BR9901089A (es)
CA (1) CA2268680A1 (es)
CO (1) CO5070713A1 (es)
DZ (1) DZ2757A1 (es)
EA (1) EA002777B1 (es)
EG (1) EG22263A (es)
GT (1) GT199900046A (es)
HR (1) HRP990105A2 (es)
HU (1) HUP9901041A3 (es)
ID (1) ID23337A (es)
IL (1) IL129328A0 (es)
IN (1) IN192342B (es)
IS (1) IS5019A (es)
MA (1) MA24831A1 (es)
NO (1) NO991672L (es)
NZ (1) NZ335104A (es)
OA (1) OA11031A (es)
PA (1) PA8469301A1 (es)
PE (1) PE20000418A1 (es)
PL (1) PL332450A1 (es)
SG (1) SG125880A1 (es)
SK (1) SK43699A3 (es)
TN (1) TNSN99052A1 (es)
TR (1) TR199900755A3 (es)
TW (1) TW448147B (es)
UA (1) UA57750C2 (es)
UY (1) UY25460A1 (es)
YU (1) YU18199A (es)
ZA (1) ZA992631B (es)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB9918684D0 (en) 1999-08-09 1999-10-13 Novartis Ag Organic compounds
US6458822B2 (en) 2000-03-13 2002-10-01 Pfizer Inc. 2-oxo-imidazolidine-4-carboxylic acid hydroxamide compounds that inhibit matrix metalloproteinases
GB0103303D0 (en) 2001-02-09 2001-03-28 Novartis Ag Organic compounds
WO2004106319A1 (en) * 2003-05-30 2004-12-09 Pfizer Products Inc. Crystal forms of 4-[4-(4-fluorophenoxy)benzenesulfonylamino]-tetrahydropyran-4-carboxylic acid hydroxyamide
AU2003264355A1 (en) * 2003-08-29 2005-03-29 Basf Aktiengesellschaft Process for production of o-substituted hydroxylamines
EP3082526A4 (en) 2013-12-18 2017-07-05 Brita LP Lid for filter-as-you-pour container system
TW202237119A (zh) 2020-12-10 2022-10-01 美商住友製藥腫瘤公司 Alk﹘5抑制劑和彼之用途

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ZA794723B (en) 1978-09-11 1980-08-27 Univ Miami Anti-hypertensive agents
GB9000725D0 (en) 1990-01-12 1990-03-14 Pfizer Ltd Therapeutic agents
US5552419A (en) * 1993-01-06 1996-09-03 Ciba-Geigy Corporation Arylsulfonamido-substituted hydroxamic acids
US5863949A (en) 1995-03-08 1999-01-26 Pfizer Inc Arylsulfonylamino hydroxamic acid derivatives
SK21499A3 (en) 1996-08-23 2000-05-16 Pfizer Arylsulfonylamino hydroxamic acid derivatives
DE69817801T2 (de) 1997-02-03 2004-03-11 Pfizer Products Inc., Groton Arylsulfonylhydroxamsäurederivate
ATE217863T1 (de) 1997-08-08 2002-06-15 Pfizer Prod Inc Arylsulfonylaminohydroxamsäurederivate
TR200000368T2 (tr) 1997-08-08 2000-07-21 Pfizer Products Inc. Ariloksiariarilsülfonilamino hidroksamik asit türevleri.
PA8469401A1 (es) 1998-04-10 2000-05-24 Pfizer Prod Inc Derivados biciclicos del acido hidroxamico

Also Published As

Publication number Publication date
ZA992631B (en) 2000-10-09
HUP9901041A3 (en) 2003-02-28
CA2268680A1 (en) 1999-10-10
TR199900755A2 (xx) 1999-11-22
HUP9901041A2 (hu) 2000-03-28
BG103319A (en) 2001-08-31
TNSN99052A1 (fr) 2005-11-10
NZ335104A (en) 2000-10-27
ID23337A (id) 2000-04-05
AU2369099A (en) 1999-10-21
EA199900284A2 (ru) 1999-10-28
AP1203A (en) 2003-09-05
GT199900046A (es) 2000-09-15
JPH11343277A (ja) 1999-12-14
HRP990105A2 (en) 2000-02-29
US6288246B1 (en) 2001-09-11
IS5019A (is) 1999-10-11
HU9901041D0 (en) 1999-06-28
AR018180A1 (es) 2001-10-31
IL129328A0 (en) 2000-02-17
AU747629B2 (en) 2002-05-16
KR19990083051A (ko) 1999-11-25
EA002777B1 (ru) 2002-08-29
NO991672D0 (no) 1999-04-09
EP0949244A2 (en) 1999-10-13
EP0949244A3 (en) 2001-05-30
UA57750C2 (uk) 2003-07-15
DZ2757A1 (fr) 2003-09-15
TR199900755A3 (tr) 1999-11-22
OA11031A (en) 2002-02-07
AP9901503A0 (en) 1999-06-30
PE20000418A1 (es) 2000-05-23
BG64154B1 (bg) 2004-02-27
UY25460A1 (es) 1999-11-17
BR9901089A (pt) 2000-05-30
SG125880A1 (en) 2006-10-30
EG22263A (en) 2002-11-30
PA8469301A1 (es) 2000-09-29
EA199900284A3 (ru) 2000-04-24
PL332450A1 (en) 1999-10-11
SK43699A3 (en) 2000-06-12
TW448147B (en) 2001-08-01
CN1232023A (zh) 1999-10-20
KR100329902B1 (ko) 2002-03-22
NO991672L (no) 1999-10-11
YU18199A (sh) 2002-11-15
MA24831A1 (fr) 1999-12-31
IN192342B (es) 2004-04-10

Similar Documents

Publication Publication Date Title
RU2406722C2 (ru) Соли бис-(тиогидразидамида) для лечения рака
AR057032A1 (es) Tigeciclina y metodos de preparacion
ES2582471T3 (es) Inhibidores polibásicos de la bomba de flujo de salida bacteriana que contienen boro y usos terapéuticos de los mismos
ES2788673T3 (es) Proceso de preparación de N-boc bifenil alaninol
AR060489A1 (es) Derivados del acido benzoazepin - oxi- acetico como agonistas de ppar - delta usados para aumentar hdl- c, reducir ldl-c y reducir colesterol
PE20040164A1 (es) Mimeticos de glucocorticoides, procedimientos para su preparacion y composiciones farmaceuticas
AR044694A1 (es) Proceso y compuestos intermedios para la preparacion de (1r, 2s,5s) - 3 azabiciclo [3,1,0] hexano-2- carboxamida, n- [3- amino-1- (ciclobutilmetil) - 2, 3 - dioxopropil] -3- [ (2s) - 2 - [[ [ 1,1- dimetiletil] amino] carbonilamino] -3,3-dimetil -1- oxobutil]-6,6 dimetilo
AR054881A1 (es) Inhibidores macrociclicos de la replicacion del virus de la hepatitis c, un proceso para su preparacion, una composicion farmaceutica que lo comprende y su uso para la elaboracion de un medicamento para el tratamiento de la hepatitis c
BRPI0612926B8 (pt) compostos fluorados de 4-(2-amino-1-hidroxietila)fenol como agonistas de receptores b2 adrenérgicos, composição farmacêutica, combinação e uso de um composto
ES2568878T3 (es) Inversión del bloqueo neuromuscular inducido por fármacos usando contenedores moleculares de cucurbit[n]urilo novedosos
AR039150A1 (es) Piridinoilpiperidinas como agonistas de 5-ht1f
BR112012007305A2 (pt) maitansinoides e o uso dos ditos maitansinoides para preparar conjugados com um anticorpo.
BRPI0516911A (pt) método para a preparação de um composto e composto de anilina
AR057383A1 (es) Compuestos quimicos derivados de 2-azetidinona, formulacion farmaceutica y un proceso de preparacion del compuesto
AR079205A1 (es) Morfolinotiazoles como moduladores alostericos positivos alfa 7
AR057380A1 (es) Compuestos quimicos derivados de 2-azetidinona y uso terapeutico de los mismos
AR115561A1 (es) Aditivos para combustible de amonio cuaternario
GT200300010A (es) Esteres hidroxamato del acido n-(4-fenil sustituido)-antranilico
AR051373A1 (es) Procedimiento para la preparacion de analogos aciclicos de nucleotidos de fosfonatos
EA201291370A1 (ru) Способ получения плеуромутилинов
BR112018076686A2 (pt) composição para a remoção de composto que contém enxofre
CO5070713A1 (es) Procedimiento para la preparacion de acidos hidroxamicos
AR070885A1 (es) Compuestos de azaindol para el tratamiento de trastornos del sistema nervioso central
AR049668A1 (es) Proceso quimico para preparar esteres de 4,4 - difluorometil - 3 - oxo - butanoico por reaccion entre una amida y un ester.
AR091075A1 (es) Proceso para preparar derivados monociclicos de heteroaril-cicloalquil-diamina