HK5493A - (s)-(-)-1-propyl-2',6'-pipecoloxylidide hydrochloride monohydrate, process for its preparation and pharmaceutical preparation containing it - Google Patents
(s)-(-)-1-propyl-2',6'-pipecoloxylidide hydrochloride monohydrate, process for its preparation and pharmaceutical preparation containing it Download PDFInfo
- Publication number
- HK5493A HK5493A HK54/93A HK5493A HK5493A HK 5493 A HK5493 A HK 5493A HK 54/93 A HK54/93 A HK 54/93A HK 5493 A HK5493 A HK 5493A HK 5493 A HK5493 A HK 5493A
- Authority
- HK
- Hong Kong
- Prior art keywords
- propyl
- water
- preparation
- compound
- added
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D211/36—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D211/60—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
-
- 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
- A61P25/02—Drugs for disorders of the nervous system for peripheral neuropathies
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Neurosurgery (AREA)
- Biomedical Technology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Neurology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Hydrogenated Pyridines (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Claims (9)
1. Chlorhydrate de (S)-(-)-1-propyl-2',6'-pipéco- loxylidide, caractérisé en ce que le composé est sous la forme de son monohydrate.
2. Composé selon la revendication 1, caractérisé en ce qu'il est pratiquement pur optiquement.
3. Composé selon la revendication 1, caractérisé en ce qu'il contient moins de 0,5% en poids de l'énan- tiomère (R)-(+) correspondant.
4. Procédé pour la préparation du monohydrate du chlorhydrate de (S)-( )-1-propyl-2',6'-pipéco- loxylidide pratiquement pur optiquement, caractérisé en ce que l'on dissout dans de l'eau du chlorhydrate de (S)-(-)-1-propyl-2'-6'-pipécoloxylidide contenant l'énantiomère (R)-(+), puis on ajoute de l'acétone chauffée à une température dans la plage de 45°C à son point d'ébullition, et on isole le monohydrate du chlorhydrate de (S)-(-)-1-propyl-2',6'- pipécoloxylidide.
5. Procédé selon la revendication 4, caractérisé en ce que l'on dissout le chlorhydrate du (S)-(-)-1-propyl-2',6'-pipécoloxylidide dans une quantité d'eau qui correspond à 1-3 fois sont poids, on ajoute de l'acétone en un volume égal à 5-15 fois le volume d'eau, à la suite de quoi on filtre la solution et on isole le produit final.
6. Procédé selon la revendication 5, caractérisé en ce que le poids de l'eau est égal au poids du chlorhydrate du (S)-(-)-1 -propyi-2',6'-pipécoioxyii- dide et le volume de l'acétone est égal à 10 fois le volume de l'eau ajoutée.
7. Composition pharmaceutique pour anesthésie locale, caractérisée en ce qu'elle contient le composé selon la revendication 1.
8. Composition selon la revendication 1, pour utilisation dans l'induction d'anesthésie locale.
9. Utilisation du composé selon la revendication 1 dans la fabrication de compositions pharmaceutiques ayant un effet anesthésique local.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SE8600017A SE451840B (sv) | 1986-01-03 | 1986-01-03 | Optiskt rent monohydrat av s-(-)-1-propyl-2',6'-pipekoloxylididhydroklorid, sett att framstella denna och farmaceutiska beredningar for lokalbedovning |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| HK5493A true HK5493A (en) | 1993-01-29 |
Family
ID=20363001
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| HK54/93A HK5493A (en) | 1986-01-03 | 1993-01-21 | (s)-(-)-1-propyl-2',6'-pipecoloxylidide hydrochloride monohydrate, process for its preparation and pharmaceutical preparation containing it |
Country Status (29)
| Country | Link |
|---|---|
| US (1) | US4870086A (fr) |
| EP (1) | EP0239710B1 (fr) |
| JP (1) | JPH07598B2 (fr) |
| KR (1) | KR940008302B1 (fr) |
| AR (1) | AR242561A1 (fr) |
| AT (1) | ATE56956T1 (fr) |
| AU (1) | AU592392B2 (fr) |
| BG (1) | BG62066B2 (fr) |
| CA (1) | CA1276154C (fr) |
| CY (1) | CY1680A (fr) |
| DE (1) | DE3674582D1 (fr) |
| DK (1) | DK171378B1 (fr) |
| EG (1) | EG17867A (fr) |
| ES (1) | ES2036179T3 (fr) |
| FI (1) | FI83075C (fr) |
| GR (1) | GR3002516T3 (fr) |
| HK (1) | HK5493A (fr) |
| IE (1) | IE59061B1 (fr) |
| LU (1) | LU88843I2 (fr) |
| LV (1) | LV5765B4 (fr) |
| MY (1) | MY101132A (fr) |
| NL (1) | NL960005I2 (fr) |
| NO (2) | NO170330C (fr) |
| NZ (1) | NZ218615A (fr) |
| PH (1) | PH22924A (fr) |
| PT (1) | PT84041B (fr) |
| SE (1) | SE451840B (fr) |
| SG (1) | SG117292G (fr) |
| ZA (1) | ZA868600B (fr) |
Families Citing this family (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SI9111010B (sl) * | 1990-06-07 | 2005-02-28 | Astrazeneca Ab | 3,5-disubstituirani indolni derivati kot "5-HT1-podobni" receptorski agonisti |
| US5834490A (en) * | 1993-11-04 | 1998-11-10 | Instituto De Investigacion Y Desarrolo Quimico Biologico, S.A. | Cyclopropyl derivatives, preparation method there-of and applications |
| ES2082703B1 (es) * | 1993-11-04 | 1996-12-16 | Inst Investigacion Desarrollo | Nuevos derivados de ciclopropilo, procedimientos para su preparacion y aplicaciones. |
| KR100393133B1 (ko) * | 1994-09-23 | 2003-11-17 | 다윈 디스커버리 리미티드 | 레보부피바카인및그의유사체의제조에사용하는라세미화및비대칭변환방법 |
| SE9501808D0 (sv) * | 1995-05-16 | 1995-05-16 | Astra Ab | New process |
| US7799337B2 (en) | 1997-07-21 | 2010-09-21 | Levin Bruce H | Method for directed intranasal administration of a composition |
| SE9800139D0 (sv) | 1998-01-21 | 1998-01-21 | Astra Ab | New use |
| BRPI0104491B8 (pt) * | 2001-10-10 | 2021-05-25 | Cristalia Produtos Quim Farmaceuticos Ltda | n-(2,6-dimetilfenil)-1-propil-2-piperidinocarboxamida; processo de obtenção dos enantiômeros; mistura não racêmica dos anantiômeros e seu processo de obtenção e composição farmacêutica. |
| US20060270708A1 (en) * | 2005-05-25 | 2006-11-30 | Navinta Llc | Novel process for preparation of isotonic aqueous injection of ropivacaine |
| US7683175B2 (en) * | 2005-06-06 | 2010-03-23 | Navinta, Llc | Process of making optically pure L-pipecolic acid and process of making anesthetics and intermediates therefrom |
| US20090187024A1 (en) * | 2006-04-25 | 2009-07-23 | Dishman Pharmaceuticals And Chemicals Ltd. | Ropivacaine hydrochloride anhydrate and the preparation thereof |
| WO2009089841A1 (fr) * | 2008-01-15 | 2009-07-23 | Pharmathen S.A. | Procédé de préparation d'un composé (s)-1-alkyl-2',6'-pipécoloxylidide |
| US8473062B2 (en) | 2008-05-01 | 2013-06-25 | Autonomic Technologies, Inc. | Method and device for the treatment of headache |
| US8412336B2 (en) | 2008-12-29 | 2013-04-02 | Autonomic Technologies, Inc. | Integrated delivery and visualization tool for a neuromodulation system |
| US8494641B2 (en) | 2009-04-22 | 2013-07-23 | Autonomic Technologies, Inc. | Implantable neurostimulator with integral hermetic electronic enclosure, circuit substrate, monolithic feed-through, lead assembly and anchoring mechanism |
| US9320908B2 (en) | 2009-01-15 | 2016-04-26 | Autonomic Technologies, Inc. | Approval per use implanted neurostimulator |
| CN102093284B (zh) * | 2010-12-29 | 2013-05-08 | 宜昌人福药业有限责任公司 | 富集哌啶-2-甲酰苯胺类旋光化合物的方法 |
Family Cites Families (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2248018A (en) * | 1939-03-30 | 1941-07-01 | Winthrop Chem Co Inc | 4-aryl-piperidine-ketones and a process of preparing them |
| GB775749A (en) * | 1955-04-06 | 1957-05-29 | Bofors Ab | Method of preparing amides of n-alkyl piperidine monocarboxylic acid and n-alkyl pyrrolidine -a-monocarboxylic acid |
| GB775750A (en) * | 1955-04-28 | 1957-05-29 | Bofors Ab | Method of preparing amides of n-alkyl piperidine mono-carboxylic acid and n-alkyl pyrrolidine -a-monocarboxylic acid |
| US2799679A (en) * | 1955-04-28 | 1957-07-16 | Bofors Ab | Process of preparing amides of heterocyclic carboxylic acids |
| GB800565A (en) * | 1956-01-23 | 1958-08-27 | Bofors Ab | Method of producing n-alkyl-piperidine-ª‡-monocarboxylic acid amides and n-alkyl-pyrrolidine-ª‡-monocarboxylic acid amides |
| GB824542A (en) * | 1957-05-15 | 1959-12-02 | Bofors Ab | Method of producing n-alkyl-piperidine-alpha-monocarboxylic acid amides |
| GB869978A (en) * | 1958-03-13 | 1961-06-07 | Bofors Ab | Method of producing n-alkyl-and-cycloalkyl-piperidine carboxylic acid amides |
| GB949729A (en) * | 1960-11-15 | 1964-02-19 | Bofors Ab | Substituted-piperidine carboxylic acid amide salts and their preparation |
| SE341404B (fr) * | 1967-05-18 | 1971-12-27 | Sterling Drug Inc | |
| CH491915A (de) * | 1967-06-28 | 1970-06-15 | Geigy Ag J R | Verfahren zur Herstellung von neuen Piperidinderivaten |
| US3879382A (en) * | 1971-08-27 | 1975-04-22 | Teijin Ltd | Process for the recovery of D- or L-{60 -amino-{68 -caprolactam hydrochloride of enhanced optical purity from mixtures of D- and L-{60 -amino-{68 -caprolactam hydrochloride |
| SE7607114L (sv) * | 1976-06-22 | 1977-12-23 | Bofors Ab | Sett att framstella hydrokloriden av n-metylpiperidin-2-karbonsyra-2,6-xyllidid |
| SE431092B (sv) * | 1979-07-10 | 1984-01-16 | Thuresson Af Ekenstam Bo | Terapeutiskt aktiva, substituerade piperidinkarboxianilider |
| JPS60502054A (ja) * | 1983-08-01 | 1985-11-28 | アストラ・レケメデル・アクチボラグ | L―N―n―プロピルピペコリン酸―2,6―キシリダイドおよびその製造方法 |
-
1986
- 1986-01-03 SE SE8600017A patent/SE451840B/sv not_active IP Right Cessation
- 1986-11-12 ZA ZA868600A patent/ZA868600B/xx unknown
- 1986-11-24 US US06/934,114 patent/US4870086A/en not_active Expired - Lifetime
- 1986-12-02 EG EG747/86A patent/EG17867A/xx active
- 1986-12-03 NO NO864858A patent/NO170330C/no not_active IP Right Cessation
- 1986-12-12 AU AU66449/86A patent/AU592392B2/en not_active Expired
- 1986-12-12 NZ NZ218615A patent/NZ218615A/xx unknown
- 1986-12-15 ES ES198686850440T patent/ES2036179T3/es not_active Expired - Lifetime
- 1986-12-15 EP EP86850440A patent/EP0239710B1/fr not_active Expired - Lifetime
- 1986-12-15 DE DE8686850440T patent/DE3674582D1/de not_active Expired - Lifetime
- 1986-12-15 PH PH34593A patent/PH22924A/en unknown
- 1986-12-15 AT AT86850440T patent/ATE56956T1/de active
- 1986-12-26 JP JP61308983A patent/JPH07598B2/ja not_active Expired - Lifetime
- 1986-12-30 MY MYPI86000260A patent/MY101132A/en unknown
- 1986-12-30 CA CA000526453A patent/CA1276154C/fr not_active Expired - Lifetime
- 1986-12-31 KR KR1019860011720A patent/KR940008302B1/ko not_active Expired - Lifetime
- 1986-12-31 PT PT84041A patent/PT84041B/pt unknown
-
1987
- 1987-01-02 FI FI870003A patent/FI83075C/fi not_active IP Right Cessation
- 1987-01-02 IE IE487A patent/IE59061B1/en not_active IP Right Cessation
- 1987-01-02 DK DK000287A patent/DK171378B1/da not_active IP Right Cessation
-
1988
- 1988-12-17 AR AR88306211A patent/AR242561A1/es active
-
1990
- 1990-11-08 GR GR90400889T patent/GR3002516T3/el unknown
-
1992
- 1992-11-06 SG SG1172/92A patent/SG117292G/en unknown
-
1993
- 1993-01-21 HK HK54/93A patent/HK5493A/en not_active IP Right Cessation
- 1993-10-10 CY CY1680A patent/CY1680A/xx unknown
-
1994
- 1994-02-18 BG BG098494A patent/BG62066B2/bg unknown
-
1996
- 1996-03-26 NL NL960005C patent/NL960005I2/nl unknown
- 1996-07-17 LV LV960261A patent/LV5765B4/xx unknown
- 1996-11-27 LU LU88843C patent/LU88843I2/fr unknown
-
1997
- 1997-07-31 NO NO1997009C patent/NO1997009I1/no unknown
Also Published As
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PF | Patent in force | ||
| PE | Patent expired |
Effective date: 20061214 |