AR017199A1 - Sal de monofosfato de isopropil-metil-[2-(3-n-propoxifenoxi)etil]-amina, proceso para su preparacion, formulacion farmaceutica que los contiene y su uso enel tratamiento del dolor. - Google Patents

Sal de monofosfato de isopropil-metil-[2-(3-n-propoxifenoxi)etil]-amina, proceso para su preparacion, formulacion farmaceutica que los contiene y su uso enel tratamiento del dolor.

Info

Publication number
AR017199A1
AR017199A1 ARP980106241A ARP980106241A AR017199A1 AR 017199 A1 AR017199 A1 AR 017199A1 AR P980106241 A ARP980106241 A AR P980106241A AR P980106241 A ARP980106241 A AR P980106241A AR 017199 A1 AR017199 A1 AR 017199A1
Authority
AR
Argentina
Prior art keywords
ethyl
amine
methyl
propoxyphenoxy
preparation
Prior art date
Application number
ARP980106241A
Other languages
English (en)
Original Assignee
Astrazeneca Ab
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 Astrazeneca Ab filed Critical Astrazeneca Ab
Publication of AR017199A1 publication Critical patent/AR017199A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C217/00Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton
    • C07C217/02Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton
    • C07C217/04Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated
    • C07C217/06Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated having only one etherified hydroxy group and one amino group bound to the carbon skeleton, which is not further substituted
    • C07C217/14Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated having only one etherified hydroxy group and one amino group bound to the carbon skeleton, which is not further substituted the oxygen atom of the etherified hydroxy group being further bound to a carbon atom of a six-membered aromatic ring
    • C07C217/18Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated having only one etherified hydroxy group and one amino group bound to the carbon skeleton, which is not further substituted the oxygen atom of the etherified hydroxy group being further bound to a carbon atom of a six-membered aromatic ring the six-membered aromatic ring or condensed ring system containing that ring being further substituted
    • C07C217/20Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated having only one etherified hydroxy group and one amino group bound to the carbon skeleton, which is not further substituted the oxygen atom of the etherified hydroxy group being further bound to a carbon atom of a six-membered aromatic ring the six-membered aromatic ring or condensed ring system containing that ring being further substituted by halogen atoms, by trihalomethyl, nitro or nitroso groups, or by singly-bound oxygen atoms
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P23/00Anaesthetics
    • A61P23/02Local anaesthetics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/04Centrally acting analgesics, e.g. opioids

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Anesthesiology (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Engineering & Computer Science (AREA)
  • Pain & Pain Management (AREA)
  • Biomedical Technology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Neurosurgery (AREA)
  • Neurology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

Sal de monofosfato de isopropil-metil-[2-(3-n-propoxifenoxi)etil]amina; proceso para la preparacion de dicha sal de monofosfato de isopropil-metil-[2-(3-n-propoxifenoxi)etil]amina; formulacion farmacéutica que la contiene y su uso en medicina. Laiso propil-metil-[2-(3-n-propoxifenoxi)etil]amina es uncompuesto con propiedades anestésicas; util comocompuesto anestésico para el tratamiento del dolor, incluso del dolor localizado. La sal cristalina demonofosfato deisopropil-metil-[2-(3-n-propoxifen oxi)etil]amina se puede utilizar para introducir un intermediario cristalino en el proceso para la preparacionde isopropil-metil-[2-(3-n-propoxifenoxi)etil]amina. Esto agrega un sencillo y conveniente paso depurificacion en una secuencia de reaccion es en la que todoslos demás intermediarios son jarabes. De esa manera, se evita la destilacion de los procesos de la técnica anterior que tanto tiempo y energía consume. Lacristalizacion de la sal demonofosfato de isopropil-metil[2-(3-n-propoxifen oxi)etil]amina a origen a un intermediario de alta pureza que puede convertirse asu vez a la correspondiente isopropil-metil-[2-(3-n-propoxifenoxi)etil]amina mediante un sencillo paso dealcalinizacion.
ARP980106241A 1997-12-22 1998-12-09 Sal de monofosfato de isopropil-metil-[2-(3-n-propoxifenoxi)etil]-amina, proceso para su preparacion, formulacion farmaceutica que los contiene y su uso enel tratamiento del dolor. AR017199A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
SE9704835A SE9704835D0 (sv) 1997-12-22 1997-12-22 New compound

Publications (1)

Publication Number Publication Date
AR017199A1 true AR017199A1 (es) 2001-08-22

Family

ID=20409538

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP980106241A AR017199A1 (es) 1997-12-22 1998-12-09 Sal de monofosfato de isopropil-metil-[2-(3-n-propoxifenoxi)etil]-amina, proceso para su preparacion, formulacion farmaceutica que los contiene y su uso enel tratamiento del dolor.

Country Status (22)

Country Link
US (1) US6235792B1 (es)
EP (1) EP1047663A1 (es)
JP (1) JP2001526254A (es)
KR (1) KR20010033407A (es)
CN (1) CN1280559A (es)
AR (1) AR017199A1 (es)
AU (1) AU1989299A (es)
BR (1) BR9814381A (es)
CA (1) CA2314989A1 (es)
EE (1) EE200000384A (es)
HU (1) HUP0004428A3 (es)
ID (1) ID26940A (es)
IL (1) IL136829A0 (es)
IS (1) IS5544A (es)
NO (1) NO20003216L (es)
PL (1) PL341525A1 (es)
SE (1) SE9704835D0 (es)
SK (1) SK8062000A3 (es)
TR (1) TR200002012T2 (es)
TW (1) TW455590B (es)
WO (1) WO1999032431A1 (es)
ZA (1) ZA9811237B (es)

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CH380746A (de) * 1958-11-06 1964-08-15 Ciba Geigy Verfahren zur Herstellung neuer sekundärer Amine
AR004691A1 (es) * 1995-10-27 1999-03-10 Astrazeneca Ab Nuevos derivados de [3-alcoxi-fenoxi-)-etil]-dialquilamina, una composicion farmaceutica que los comprende, su uso como anestesicos locales y unprocedimiento para su preparacion

Also Published As

Publication number Publication date
SK8062000A3 (en) 2001-02-12
KR20010033407A (ko) 2001-04-25
NO20003216D0 (no) 2000-06-21
ID26940A (id) 2001-02-22
SE9704835D0 (sv) 1997-12-22
NO20003216L (no) 2000-06-21
IL136829A0 (en) 2001-06-14
US6235792B1 (en) 2001-05-22
WO1999032431A1 (en) 1999-07-01
TW455590B (en) 2001-09-21
CN1280559A (zh) 2001-01-17
AU1989299A (en) 1999-07-12
BR9814381A (pt) 2000-10-10
EP1047663A1 (en) 2000-11-02
HUP0004428A2 (hu) 2002-03-28
PL341525A1 (en) 2001-04-23
TR200002012T2 (tr) 2000-10-23
CA2314989A1 (en) 1999-07-01
ZA9811237B (en) 1999-07-19
EE200000384A (et) 2001-12-17
JP2001526254A (ja) 2001-12-18
HUP0004428A3 (en) 2002-04-29
IS5544A (is) 2000-06-21

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