ES2119990T3 - Procedimiento mejorado para la preparacion de derivados de cloruro de propargilamonio. - Google Patents
Procedimiento mejorado para la preparacion de derivados de cloruro de propargilamonio.Info
- Publication number
- ES2119990T3 ES2119990T3 ES94890207T ES94890207T ES2119990T3 ES 2119990 T3 ES2119990 T3 ES 2119990T3 ES 94890207 T ES94890207 T ES 94890207T ES 94890207 T ES94890207 T ES 94890207T ES 2119990 T3 ES2119990 T3 ES 2119990T3
- Authority
- ES
- Spain
- Prior art keywords
- general formula
- isomero
- amino
- iii
- general
- Prior art date
- Legal status (The legal status 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 status listed.)
- Expired - Lifetime
Links
- 238000000034 method Methods 0.000 title abstract 3
- 238000002360 preparation method Methods 0.000 title abstract 2
- IKXNIQJDNKPPCH-UHFFFAOYSA-N hydron;prop-2-yn-1-amine;chloride Chemical class [Cl-].[NH3+]CC#C IKXNIQJDNKPPCH-UHFFFAOYSA-N 0.000 title 1
- -1 AMINO Chemical class 0.000 abstract 6
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 abstract 2
- 239000000908 ammonium hydroxide Substances 0.000 abstract 2
- 238000006243 chemical reaction Methods 0.000 abstract 2
- 150000004820 halides Chemical class 0.000 abstract 2
- FEWJPZIEWOKRBE-LWMBPPNESA-N levotartaric acid Chemical group OC(=O)[C@@H](O)[C@H](O)C(O)=O FEWJPZIEWOKRBE-LWMBPPNESA-N 0.000 abstract 2
- 239000000203 mixture Substances 0.000 abstract 2
- 238000000926 separation method Methods 0.000 abstract 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 abstract 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 abstract 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 abstract 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 abstract 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical class [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical class OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 abstract 1
- 150000001412 amines Chemical class 0.000 abstract 1
- 150000003863 ammonium salts Chemical class 0.000 abstract 1
- 239000007864 aqueous solution Substances 0.000 abstract 1
- 238000000354 decomposition reaction Methods 0.000 abstract 1
- 238000004821 distillation Methods 0.000 abstract 1
- 229910052731 fluorine Inorganic materials 0.000 abstract 1
- 239000011737 fluorine Substances 0.000 abstract 1
- 159000000011 group IA salts Chemical class 0.000 abstract 1
- 150000002367 halogens Chemical group 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 239000001257 hydrogen Substances 0.000 abstract 1
- 229910000041 hydrogen chloride Inorganic materials 0.000 abstract 1
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 abstract 1
- 239000010410 layer Substances 0.000 abstract 1
- 239000012044 organic layer Substances 0.000 abstract 1
- 239000003960 organic solvent Substances 0.000 abstract 1
- 239000000243 solution Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C209/00—Preparation of compounds containing amino groups bound to a carbon skeleton
- C07C209/04—Preparation of compounds containing amino groups bound to a carbon skeleton by substitution of functional groups by amino groups
- C07C209/06—Preparation of compounds containing amino groups bound to a carbon skeleton by substitution of functional groups by amino groups by substitution of halogen atoms
- C07C209/08—Preparation of compounds containing amino groups bound to a carbon skeleton by substitution of functional groups by amino groups by substitution of halogen atoms with formation of amino groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C211/00—Compounds containing amino groups bound to a carbon skeleton
- C07C211/01—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to acyclic carbon atoms
- C07C211/26—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to acyclic carbon atoms of an unsaturated carbon skeleton containing at least one six-membered aromatic ring
- C07C211/27—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to acyclic carbon atoms of an unsaturated carbon skeleton containing at least one six-membered aromatic ring having amino groups linked to the six-membered aromatic ring by saturated carbon chains
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C211/00—Compounds containing amino groups bound to a carbon skeleton
- C07C211/01—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to acyclic carbon atoms
- C07C211/26—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to acyclic carbon atoms of an unsaturated carbon skeleton containing at least one six-membered aromatic ring
- C07C211/29—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to acyclic carbon atoms of an unsaturated carbon skeleton containing at least one six-membered aromatic ring the carbon skeleton being further substituted by halogen atoms or by nitro or nitroso groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Treatment Of Steel In Its Molten State (AREA)
Abstract
LA PRESENTE INVENCION SE REFIERE A UN PROCESO PARA LA PREPARACION DE DERIVADOS DE L-ISOMERO DE CLORURO DE AMONIO DE PROPARGILO DE LA FORMULA GENERAL (I) MEDIANTE LA DESCOMPOSICION DE D-TARTARATO DE L-ISOMERO DEL AMINO DE LA FORMULA GENERAL (II) Y MEDIANTE LA REACCION DEL AMINO DE L-ISOMERO OBTENIDO DE LA FORMULA GENERAL (II) EN PRESENCIA DE UNA BASE CON UN HALURO DE LA FORMULA GENERAL (V), Y MEDIANTE LA REACCION DEL L-ISOMERO ASI OBTENIDO DE LA FORMULA GENERAL (III) CON CLORURO DE HIDROGENO EN UN DISOLVENTE ORGANICO, EN DONDE -X REPRESENTA UN ATOMO HALOGENO, -Y REPRESENTA UN ATOMO DE HIDROGENO O DE FLUOR QUE COMPRENDE LA LIBERACION DE LA BASE AMINA DEL D-TARTARATO DEL L-ISOMERO DEL AMINO DE LA FORMULA GENERAL (II), EN DONDE Y ES COMO SE MUESTRA ARRIBA, EN SOLUCION ACUOSA CON HIDROXIDO DE AMONIO O SAL ALCALINA BASICA Y/O SAL DE AMONIO, Y REACCIONANDO LA MISMA CON 1-1,5 MOL EQUIVALENTE A UN HALURO DE LA FORMULA GENERAL (V), EN DONDE -X ES COMO SE DEFINE ARRIBA A 0-50 (GRADOS) C EN UN SISTEMADE SEPARACION DEL PH DE 8-12 DIRECTAMENTE FORMADO EN EL CURSO DE LA LIBERACION DE LA BASE Y DESPUES DE LA SEPARACION DE LA CAPA ACUOSA EXTRAYENDO LA MEZCLA QUE CONTIENE AMINOS DE L-ISOMERO DE LAS FORMULAS GENERALES (II) Y (III) EN LA CAPA ORGANICA CON AGUA Y CON UNA MEZCLA DE HIDROXIDO DE AMONIO Y AGUA Y/O CON UNA SOLUCION DE SAL DE FOSFATO ACUOSO DE UN PH DE 5,5-7,5 Y DISOLVIENDO EL AMINO DE L-ISOMERO DE LA FORMULA GENERAL (II) O SALES DEL MISMO EN LA CAPA ACUOSA Y SEPARANDOLO SELECTIVAMENTE DEL AMINO DE L-ISOMERO DE LA FORMULA GENERAL (III) Y CONVIRTIENDO EL AMINO DE L-ISOMERO DE LA FORMULA GENERAL (III) DESPUES DE LA DESTILACION A SAL DE L-ISOMERO DE LA FORMULA GENERAL (I) MEDIANTE UN METODO CONOCIDO PER SE.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
HU9403342A HU218927B (hu) | 1994-11-22 | 1994-11-22 | Eljárás propargil-ammónium-klorid-származékok előállítására |
Publications (1)
Publication Number | Publication Date |
---|---|
ES2119990T3 true ES2119990T3 (es) | 1998-10-16 |
Family
ID=10985778
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ES94890207T Expired - Lifetime ES2119990T3 (es) | 1994-11-22 | 1994-12-09 | Procedimiento mejorado para la preparacion de derivados de cloruro de propargilamonio. |
Country Status (13)
Country | Link |
---|---|
US (1) | US5449828A (es) |
EP (1) | EP0713858B1 (es) |
AT (1) | ATE168987T1 (es) |
CA (1) | CA2137761C (es) |
CZ (1) | CZ289827B6 (es) |
DE (1) | DE69412101T2 (es) |
DK (1) | DK0713858T3 (es) |
ES (1) | ES2119990T3 (es) |
GR (1) | GR3027708T3 (es) |
HU (1) | HU218927B (es) |
IL (1) | IL113298A (es) |
RU (1) | RU2130450C1 (es) |
UA (1) | UA39938C2 (es) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2006073547A1 (en) * | 2005-01-06 | 2006-07-13 | Mallinckrodt Inc. | Process for preparing benzylated amines |
CN102775317A (zh) * | 2012-07-09 | 2012-11-14 | 盐城工学院 | 一种制备烯丙基二甲基脱氢枞基氯化铵的方法 |
CN102816074A (zh) * | 2012-08-27 | 2012-12-12 | 万隆化工有限公司 | 一种对正丁基苯胺的合成方法 |
CN102850227B (zh) * | 2012-09-19 | 2015-05-13 | 常州胜杰化工有限公司 | 前手性烯丙基胺类化合物及其合成方法 |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1121857A (en) * | 1965-01-05 | 1968-07-31 | Science Union & Cie | New phenylisopropylamine derivatives and process for their preparation and pharmaceutical preparations of such derivatives |
US3485874A (en) * | 1966-05-04 | 1969-12-23 | Chinoin Gyogyszer Es Vegyeszet | Ortho and para bromophenyl isopropyl methylamines |
US3496195A (en) * | 1966-05-11 | 1970-02-17 | Chinoin Gyogyszer Es Vegyeszet | D-o-bromo-phenyl-isopropyl-methylpropinylamine and its salts |
HU187775B (en) * | 1982-07-14 | 1986-02-28 | Chinoin Gyogyszer Es Vegyeszeti Termekek Gyara Rt,Hu | New process for producing propargile-amines of pharmaceutical activity |
HU207282B (en) * | 1984-05-31 | 1993-03-29 | Chinoin Gyogyszer Es Vegyeszet | Process for producing phenyl-alkyl-amine derivatives and pharmaceutical compositions containing them |
-
1994
- 1994-11-22 HU HU9403342A patent/HU218927B/hu not_active IP Right Cessation
- 1994-12-08 UA UA94129143A patent/UA39938C2/uk unknown
- 1994-12-08 CZ CZ19943094A patent/CZ289827B6/cs not_active IP Right Cessation
- 1994-12-09 EP EP94890207A patent/EP0713858B1/en not_active Expired - Lifetime
- 1994-12-09 CA CA002137761A patent/CA2137761C/en not_active Expired - Fee Related
- 1994-12-09 DK DK94890207T patent/DK0713858T3/da active
- 1994-12-09 DE DE69412101T patent/DE69412101T2/de not_active Expired - Lifetime
- 1994-12-09 RU RU94043796A patent/RU2130450C1/ru not_active IP Right Cessation
- 1994-12-09 AT AT94890207T patent/ATE168987T1/de active
- 1994-12-09 US US08/353,816 patent/US5449828A/en not_active Expired - Lifetime
- 1994-12-09 ES ES94890207T patent/ES2119990T3/es not_active Expired - Lifetime
-
1995
- 1995-04-07 IL IL11329895A patent/IL113298A/xx not_active IP Right Cessation
-
1998
- 1998-08-20 GR GR980401885T patent/GR3027708T3/el unknown
Also Published As
Publication number | Publication date |
---|---|
DE69412101D1 (de) | 1998-09-03 |
RU2130450C1 (ru) | 1999-05-20 |
DK0713858T3 (da) | 1998-11-16 |
IL113298A0 (en) | 1995-07-31 |
CZ289827B6 (cs) | 2002-04-17 |
CA2137761A1 (en) | 1996-05-23 |
UA39938C2 (uk) | 2001-07-16 |
RU94043796A (ru) | 1996-10-10 |
GR3027708T3 (en) | 1998-11-30 |
HUT74016A (en) | 1996-10-28 |
US5449828A (en) | 1995-09-12 |
EP0713858A1 (en) | 1996-05-29 |
HU9403342D0 (en) | 1995-02-28 |
CA2137761C (en) | 1998-05-12 |
ATE168987T1 (de) | 1998-08-15 |
HU218927B (hu) | 2000-12-28 |
DE69412101T2 (de) | 1999-01-14 |
EP0713858B1 (en) | 1998-07-29 |
IL113298A (en) | 1999-09-22 |
CZ309494A3 (en) | 1996-06-12 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
FG2A | Definitive protection |
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