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
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C217/00—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton
- C07C217/02—Compounds 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
- C07C217/04—Compounds 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
- C07C217/06—Compounds 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
- C07C217/14—Compounds 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
- C07C217/18—Compounds 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
- C07C217/20—Compounds 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P23/00—Anaesthetics
- A61P23/02—Local anaesthetics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/04—Centrally 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.
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)
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 |
-
1997
- 1997-12-22 SE SE9704835A patent/SE9704835D0/xx unknown
-
1998
- 1998-12-08 ZA ZA9811237A patent/ZA9811237B/xx unknown
- 1998-12-09 TW TW087120433A patent/TW455590B/zh not_active IP Right Cessation
- 1998-12-09 AR ARP980106241A patent/AR017199A1/es not_active Application Discontinuation
- 1998-12-15 BR BR9814381-6A patent/BR9814381A/pt not_active IP Right Cessation
- 1998-12-15 AU AU19892/99A patent/AU1989299A/en not_active Abandoned
- 1998-12-15 JP JP2000525368A patent/JP2001526254A/ja active Pending
- 1998-12-15 CN CN98811771A patent/CN1280559A/zh active Pending
- 1998-12-15 TR TR2000/02012T patent/TR200002012T2/xx unknown
- 1998-12-15 WO PCT/SE1998/002316 patent/WO1999032431A1/en not_active Application Discontinuation
- 1998-12-15 US US09/254,420 patent/US6235792B1/en not_active Expired - Fee Related
- 1998-12-15 PL PL98341525A patent/PL341525A1/xx unknown
- 1998-12-15 CA CA002314989A patent/CA2314989A1/en not_active Abandoned
- 1998-12-15 EE EEP200000384A patent/EE200000384A/xx unknown
- 1998-12-15 SK SK806-2000A patent/SK8062000A3/sk unknown
- 1998-12-15 HU HU0004428A patent/HUP0004428A3/hu unknown
- 1998-12-15 EP EP98964600A patent/EP1047663A1/en not_active Ceased
- 1998-12-15 IL IL13682998A patent/IL136829A0/xx unknown
- 1998-12-15 ID IDW20001132A patent/ID26940A/id unknown
- 1998-12-15 KR KR1020007006882A patent/KR20010033407A/ko not_active Application Discontinuation
-
2000
- 2000-06-21 NO NO20003216A patent/NO20003216L/no not_active Application Discontinuation
- 2000-06-21 IS IS5544A patent/IS5544A/is unknown
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 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
BR9910921A (pt) | Composto, processo para preparar o mesmo, formulação farmacêutica, uso de um composto, e, processo para a profilaxia e/ou tratamento de condições clìnicas associadas com a resistência à insulina | |
ES2189782T3 (es) | Derivados de pteridina opticamente activos. | |
ES2082755T3 (es) | Derivados de acido 3-desmetil-mevalonico, procedimiento para su preparacion, preparados farmaceuticos a base de estos compuestos, su utilizacion asi como productos intermedios. | |
IT1256345B (it) | Esteri nitrici di derivati dell'acido 2-(2,6-di-alo-fenilammino) fenilacetico e procedimento per la loro preparazione | |
DK164937C (da) | Analogifremgangsmaade til fremstilling af 1-alkyl-2-aminotetralinderivater eller farmaceutisk acceptable syreadditionssalte deraf samt 1-alkyl-2-aminotetralinderivater til anvendelse som udgangsmateriale i fremgangsmaaden | |
BR9910928A (pt) | Composto, processo para a prepará-lo, uso do mesmo, formulação, e, processo para a profilaxia e/ou tratamento de condições clinicas associadas com resistência a insulina | |
ES2038623T3 (es) | Procedimiento para preparar soluciones de oxazafosforinas con estabilidad mejorada. | |
MY101132A (en) | An optically pure pipecoloxylidide hydrochloride and a process for its preparation | |
MX9205577A (es) | Derivados de carbamato de 4-amino-3-isoxazolidinonas, 3-amino-1-hidroxipirrolidin-2-onas y analogos del acido 1-amino-1-ciclopropanocarboxilico, un procedimiento para su preparacion y su uso como medicamentos. | |
AR017199A1 (es) | 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. | |
ES8101590A1 (es) | Un procedimiento para la preparacion de pirimido-2-benzace- pinas | |
ATE41146T1 (de) | Irreversible dopamin-b-hydroxylase-inhibitoren. | |
CA2029704A1 (en) | Pyrimidone derivatives and analogs in the treatment of asthma or certain skin disorders | |
DK0681473T3 (da) | Præparater, der indeholder tandospiron eller dets analoger | |
ES8501748A1 (es) | Un procedimiento para preparar derivados de benzamida | |
IT1188178B (it) | Sali della citidin-difospocolina particolarmente idonei per uso orale | |
NO850580L (no) | Isoksazol-derivater, fremgangsmaate til deres fremstilling, legemidler inneholdende disse forbindelser | |
PT84680B (pt) | Processo para a preparacao de derivados de 1,5-benzotiazepina e de composicoes farmaceuticas que os contem | |
AR008371A1 (es) | Una sal de adicion con acido de una 10-aminoalifatil-dibenz[b,f],oxepina, su empleo; procedimiento para su elaboracion, una 10-aminoalifatil-dibenz[b,f]oxepina, una preparacion farmaceutica que contiene dicha sal o dicha oxepina y un procedimiento para el tratamiento de enfermedades neurodegenerativ | |
FI864970A (fi) | Nya kristallina salter av aryloxi-propanolaminer, foerfarande foer deras framstaellning och deras anvaendning. | |
FI890779A (fi) | 14,17 -etano-14 -estratrieenejä, menetelmä niiden valmistamiseksi ja niitä sisältäviä, ehkäisyaineina käytettäviä valmisteita | |
BR9814496A (pt) | Composto, processos para a preparação de cristais de sementes da modificação termodinamicamente estável i de ramatroban, para a preparação de uma forma termodinamicamente estável de ramatroban, medicamento, e, uso de uma modificação termodinamicamente estável de ramatroban | |
DK364386D0 (da) | 1-alkyl-ergolinyl-thiourinstofderivater og fremgangsmaade til fremstilling deraf samt deres anvendelse | |
ES2054887T3 (es) | Nuevos 5-halogeno-tienoisotiazol-3(2h)-on-1,1-dioxidos basicamente substituidos, un procedimiento para su obtencion y los preparados farmaceuticos que contienen estos compuestos. | |
HU9603590D0 (en) | New salts of 2-[(2,6-dichloro-phenyl)-amino]-phenyl-acetoxy-acetic acid with organic bases, pharmaceutical compns. contg. them and process for preparing the said compds. |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
FA | Abandonment or withdrawal |