NO309266B1 - Fremgangsmåte for fremstilling av optisk anriket bupivacain - Google Patents

Fremgangsmåte for fremstilling av optisk anriket bupivacain Download PDF

Info

Publication number: NO309266B1
Authority: NO; Norway
Prior art keywords: solvent; bupivacaine; water; levobupivacaine; optically enriched
Prior art date: 1994-10-25

Application number

NO971903A

Other languages

English (en)

Norwegian (no)

Other versions

NO971903D0 (no

NO971903L (no

Inventor

Marianne Langston

Benjamin Mark Skead

Original Assignee

Darwin Discovery Ltd

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.)

1994-10-25

Filing date

1997-04-24

Publication date

2001-01-08

1994-10-25 Priority claimed from GB9421476A external-priority patent/GB9421476D0/en

1995-03-10 Priority claimed from GBGB9504926.8A external-priority patent/GB9504926D0/en

1997-04-24 Application filed by Darwin Discovery Ltd filed Critical Darwin Discovery Ltd

1997-04-24 Publication of NO971903D0 publication Critical patent/NO971903D0/no

1997-04-24 Publication of NO971903L publication Critical patent/NO971903L/no

2001-01-08 Publication of NO309266B1 publication Critical patent/NO309266B1/no

Links

238000000034 method Methods 0.000 title claims description 20
LEBVLXFERQHONN-UHFFFAOYSA-N 1-butyl-N-(2,6-dimethylphenyl)piperidine-2-carboxamide Chemical compound CCCCN1CCCCC1C(=O)NC1=C(C)C=CC=C1C LEBVLXFERQHONN-UHFFFAOYSA-N 0.000 title claims description 12
229960003150 bupivacaine Drugs 0.000 title claims description 10
238000002360 preparation method Methods 0.000 title description 2
239000002904 solvent Substances 0.000 claims abstract description 16
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 12
FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 claims abstract description 7
239000003795 chemical substances by application Substances 0.000 claims abstract description 6
239000011975 tartaric acid Substances 0.000 claims abstract description 6
235000002906 tartaric acid Nutrition 0.000 claims abstract description 5
238000006243 chemical reaction Methods 0.000 claims abstract description 4
229960004288 levobupivacaine Drugs 0.000 claims description 7
LEBVLXFERQHONN-INIZCTEOSA-N levobupivacaine Chemical compound CCCCN1CCCC[C@H]1C(=O)NC1=C(C)C=CC=C1C LEBVLXFERQHONN-INIZCTEOSA-N 0.000 claims description 7
238000004519 manufacturing process Methods 0.000 claims description 5
239000003960 organic solvent Substances 0.000 claims description 4
QCQCHGYLTSGIGX-GHXANHINSA-N 4-[[(3ar,5ar,5br,7ar,9s,11ar,11br,13as)-5a,5b,8,8,11a-pentamethyl-3a-[(5-methylpyridine-3-carbonyl)amino]-2-oxo-1-propan-2-yl-4,5,6,7,7a,9,10,11,11b,12,13,13a-dodecahydro-3h-cyclopenta[a]chrysen-9-yl]oxy]-2,2-dimethyl-4-oxobutanoic acid Chemical compound N([C@@]12CC[C@@]3(C)[C@]4(C)CC[C@H]5C(C)(C)[C@@H](OC(=O)CC(C)(C)C(O)=O)CC[C@]5(C)[C@H]4CC[C@@H]3C1=C(C(C2)=O)C(C)C)C(=O)C1=CN=CC(C)=C1 QCQCHGYLTSGIGX-GHXANHINSA-N 0.000 claims description 2
FEWJPZIEWOKRBE-LWMBPPNESA-N levotartaric acid Chemical group OC(=O)[C@@H](O)[C@H](O)C(O)=O FEWJPZIEWOKRBE-LWMBPPNESA-N 0.000 claims description 2
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 16
239000007787 solid Substances 0.000 description 7
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
229960001367 tartaric acid Drugs 0.000 description 5
FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 4
239000012458 free base Substances 0.000 description 4
BZLVMXJERCGZMT-UHFFFAOYSA-N Methyl tert-butyl ether Chemical compound COC(C)(C)C BZLVMXJERCGZMT-UHFFFAOYSA-N 0.000 description 3
238000002474 experimental method Methods 0.000 description 3
239000000203 mixture Substances 0.000 description 3
239000000725 suspension Substances 0.000 description 3
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
230000000052 comparative effect Effects 0.000 description 2
239000013078 crystal Substances 0.000 description 2
238000002425 crystallisation Methods 0.000 description 2
230000008025 crystallization Effects 0.000 description 2
238000004821 distillation Methods 0.000 description 2
230000000694 effects Effects 0.000 description 2
239000010410 layer Substances 0.000 description 2
230000003287 optical effect Effects 0.000 description 2
239000012044 organic layer Substances 0.000 description 2
238000000926 separation method Methods 0.000 description 2
238000003756 stirring Methods 0.000 description 2
ZKMNUMMKYBVTFN-HNNXBMFYSA-N (S)-ropivacaine Chemical compound CCCN1CCCC[C@H]1C(=O)NC1=C(C)C=CC=C1C ZKMNUMMKYBVTFN-HNNXBMFYSA-N 0.000 description 1
239000002253 acid Substances 0.000 description 1
230000001476 alcoholic effect Effects 0.000 description 1
229940035676 analgesics Drugs 0.000 description 1
239000000730 antalgic agent Substances 0.000 description 1
239000002585 base Substances 0.000 description 1
229960001050 bupivacaine hydrochloride Drugs 0.000 description 1
239000007810 chemical reaction solvent Substances 0.000 description 1
238000004296 chiral HPLC Methods 0.000 description 1
150000001875 compounds Chemical class 0.000 description 1
NTBIYBAYFBNTCD-UHFFFAOYSA-N dibenzoyl 2,3-dihydroxybutanedioate Chemical compound C=1C=CC=CC=1C(=O)OC(=O)C(O)C(O)C(=O)OC(=O)C1=CC=CC=C1 NTBIYBAYFBNTCD-UHFFFAOYSA-N 0.000 description 1
238000004090 dissolution Methods 0.000 description 1
239000007789 gas Substances 0.000 description 1
229910000041 hydrogen chloride Inorganic materials 0.000 description 1
IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 1
229960001464 levobupivacaine hydrochloride Drugs 0.000 description 1
SIEYLFHKZGLBNX-NTISSMGPSA-N levobupivacaine hydrochloride (anhydrous) Chemical compound [Cl-].CCCC[NH+]1CCCC[C@H]1C(=O)NC1=C(C)C=CC=C1C SIEYLFHKZGLBNX-NTISSMGPSA-N 0.000 description 1
239000003589 local anesthetic agent Substances 0.000 description 1
229960005015 local anesthetics Drugs 0.000 description 1
230000006340 racemization Effects 0.000 description 1
239000011541 reaction mixture Substances 0.000 description 1
238000004064 recycling Methods 0.000 description 1
229960001549 ropivacaine Drugs 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
238000003786 synthesis reaction Methods 0.000 description 1
150000003892 tartrate salts Chemical class 0.000 description 1
JCQBWMAWTUBARI-UHFFFAOYSA-N tert-butyl 3-ethenylpiperidine-1-carboxylate Chemical compound CC(C)(C)OC(=O)N1CCCC(C=C)C1 JCQBWMAWTUBARI-UHFFFAOYSA-N 0.000 description 1
231100001274 therapeutic index Toxicity 0.000 description 1

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

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Medicines Containing Material From Animals Or Micro-Organisms (AREA)
Hydrogenated Pyridines (AREA)
Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Preparation Of Compounds By Using Micro-Organisms (AREA)
Compounds Of Unknown Constitution (AREA)
Investigating Or Analysing Biological Materials (AREA)
Nitrogen Condensed Heterocyclic Rings (AREA)
Non-Silver Salt Photosensitive Materials And Non-Silver Salt Photography (AREA)
Peptides Or Proteins (AREA)
Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
Saccharide Compounds (AREA)
Epoxy Compounds (AREA)

NO971903A 1994-10-25 1997-04-24 Fremgangsmåte for fremstilling av optisk anriket bupivacain NO309266B1 (no)

Applications Claiming Priority (3)

Application Number	Priority Date	Filing Date	Title
GB9421476A GB9421476D0 (en)	1994-10-25	1994-10-25	Process and salt
GBGB9504926.8A GB9504926D0 (en)	1995-03-10	1995-03-10	Crystallisation
PCT/GB1995/002513 WO1996012699A1 (fr)	1994-10-25	1995-10-23	Cristallisation de la levobupicavaine et des analogues de celle-ci

Publications (3)

Publication Number	Publication Date
NO971903D0 NO971903D0 (no)	1997-04-24
NO971903L NO971903L (no)	1997-04-24
NO309266B1 true NO309266B1 (no)	2001-01-08

Family

ID=26305863

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO971903A NO309266B1 (no)	1994-10-25	1997-04-24	Fremgangsmåte for fremstilling av optisk anriket bupivacain

Country Status (16)

Country	Link
US (1)	US5994548A (fr)
EP (1)	EP0788480B1 (fr)
JP (1)	JP3911545B2 (fr)
AT (1)	ATE245629T1 (fr)
AU (1)	AU698637B2 (fr)
CA (1)	CA2200355C (fr)
DE (1)	DE69531356T2 (fr)
DK (1)	DK0788480T3 (fr)
ES (1)	ES2202375T3 (fr)
FI (1)	FI117438B (fr)
HU (1)	HU227420B1 (fr)
MX (1)	MX9703024A (fr)
NO (1)	NO309266B1 (fr)
PL (1)	PL183210B1 (fr)
PT (1)	PT788480E (fr)
WO (1)	WO1996012699A1 (fr)

Families Citing this family (19)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
BR0002246A (pt) *	2000-04-06	2003-04-15	Cristalia Prod Quimicos Farm	Processo de obtenção dos enantiÈmeros da bupivacaìna racêmica, processo de obtenção de composições farmacêuticas a base de levobupivacaìna: composições farmacêuticas a base de levobupivacaìna formuladas nas formas básicas ou sais farmaceuticamente aceitáveis e utilização das composições farmacêuticas a base de levobupivacaìna formuladas nas formas básicas ou sais farmaceuticamente aceitáveis
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.
US20040001889A1 (en)	2002-06-25	2004-01-01	Guohua Chen	Short duration depot formulations
EP2218448B1 (fr)	2002-12-13	2015-09-23	Durect Corporation	Forme d'administration orale de medicaments comprenant un vehicule liquide de haute viscosite
US7094812B2 (en) *	2003-04-24	2006-08-22	Xerox Corporations	Colorant compositions
US6790267B1 (en) *	2003-04-24	2004-09-14	Xerox Corporation	Colorant compositions
DK2767292T3 (en)	2004-09-17	2016-12-19	Durect Corp	RENEWABLE local anesthetic COMPOSITION CONTAINING SAIB
US20070027105A1 (en)	2005-07-26	2007-02-01	Alza Corporation	Peroxide removal from drug delivery vehicle
WO2007123405A1 (fr) *	2006-04-25	2007-11-01	Dishman Pharmaceuticals And Chemicals Ltd.	chlorhydrate de ropivacaine ANHYDRE et PRÉPARATION de celui-ci
AU2007325918B2 (en)	2006-11-03	2013-10-17	Durect Corporation	Transdermal delivery systems comprising bupivacaine
EP2067471B1 (fr)	2007-12-06	2018-02-14	Durect Corporation	Formes orales de dosage pharmaceutique
ES2383714T3 (es) *	2008-01-15	2012-06-25	Pharmathen S.A.	Proceso para preparar un compuesto (S)-1-alquil-2',6'-pipecoloxilidídico
US20100260844A1 (en)	2008-11-03	2010-10-14	Scicinski Jan J	Oral pharmaceutical dosage forms
CN103073484B (zh) *	2013-01-28	2014-10-22	山东诚创医药技术开发有限公司	一种甲哌卡因及其光学对映体的制备方法
CA2905131A1 (fr)	2013-03-15	2014-09-18	Durect Corporation	Compositions ayant un agent de modification rheologique pour reduire une variabilite de dissolution
CN109475505A (zh)	2016-07-06	2019-03-15	度瑞公司	具有药物组成物、屏障层及药物层的口服剂型
CA3048485C (fr) *	2016-12-26	2022-07-19	Cellix Bio Private Limited	Compositions et methode s pour le traitement d'une douleur chronique
WO2021146215A1 (fr)	2020-01-13	2021-07-22	Durect Corporation	Systèmes d'administration de médicament à libération prolongée avec impuretés réduites et procédés associés
CA3203561A1 (fr)	2021-01-12	2022-07-21	Adrian Neil Verity	Systemes d'administration de medicament a liberation prolongee et procedes associes

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
SE341404B (fr) *	1967-05-18	1971-12-27	Sterling Drug Inc
US4695576A (en) *	1984-07-09	1987-09-22	Astra Lake Medel Aktiebolag	L-N-n-propylpipecolic acid-2,6-xylidide

1995
- 1995-10-23 WO PCT/GB1995/002513 patent/WO1996012699A1/fr not_active Ceased
- 1995-10-23 DE DE69531356T patent/DE69531356T2/de not_active Expired - Lifetime
- 1995-10-23 PL PL95319829A patent/PL183210B1/pl unknown
- 1995-10-23 AU AU37048/95A patent/AU698637B2/en not_active Expired
- 1995-10-23 PT PT95934738T patent/PT788480E/pt unknown
- 1995-10-23 CA CA002200355A patent/CA2200355C/fr not_active Expired - Lifetime
- 1995-10-23 AT AT95934738T patent/ATE245629T1/de active
- 1995-10-23 EP EP95934738A patent/EP0788480B1/fr not_active Expired - Lifetime
- 1995-10-23 JP JP51373896A patent/JP3911545B2/ja not_active Expired - Lifetime
- 1995-10-23 US US08/849,418 patent/US5994548A/en not_active Expired - Lifetime
- 1995-10-23 MX MX9703024A patent/MX9703024A/es unknown
- 1995-10-23 HU HU9702372A patent/HU227420B1/hu unknown
- 1995-10-23 DK DK95934738T patent/DK0788480T3/da active
- 1995-10-23 ES ES95934738T patent/ES2202375T3/es not_active Expired - Lifetime
1997
- 1997-04-22 FI FI971711A patent/FI117438B/fi not_active IP Right Cessation
- 1997-04-24 NO NO971903A patent/NO309266B1/no not_active IP Right Cessation

Also Published As

Publication number	Publication date
AU3704895A (en)	1996-05-15
JP3911545B2 (ja)	2007-05-09
HUT77631A (hu)	1998-06-29
PL319829A1 (en)	1997-09-01
JPH10507464A (ja)	1998-07-21
DK0788480T3 (da)	2003-09-29
FI117438B (fi)	2006-10-13
MX9703024A (es)	1997-10-31
HU227420B1 (en)	2011-05-30
WO1996012699A1 (fr)	1996-05-02
FI971711A0 (fi)	1997-04-22
CA2200355A1 (fr)	1996-05-02
FI971711L (fi)	1997-04-22
AU698637B2 (en)	1998-11-05
EP0788480A1 (fr)	1997-08-13
PL183210B1 (pl)	2002-06-28
DE69531356T2 (de)	2004-05-27
US5994548A (en)	1999-11-30
NO971903D0 (no)	1997-04-24
EP0788480B1 (fr)	2003-07-23
DE69531356D1 (de)	2003-08-28
NO971903L (no)	1997-04-24
ES2202375T3 (es)	2004-04-01
ATE245629T1 (de)	2003-08-15
CA2200355C (fr)	2007-03-06
PT788480E (pt)	2003-12-31

Legal Events

Date	Code	Title	Description
2015-11-02	MK1K	Patent expired

Publication	Publication Date	Title
CA2200355C (fr)	2007-03-06	Cristallisation de la levobupicavaine et des analogues de celle-ci
US20060135777A1 (en)	2006-06-22	Method for the production of d-threo-2-phenyl-2-piperidine-2-yl acetates
AU696875B2 (en)	1998-09-17	New process for the preparation of ropivacaine hydrochloride monohydrate
AU2001278094B2 (en)	2006-01-12	Novel crystalline forms of 4-[4-[4-(hydroxydiphenylmethyl)-1-piperindinyl]-1-hydroxybutyl]-alpha, alpha-dimethylbenzene acetic acid and its hydrochloride
DK152752B (da)	1988-05-09	Fremgangsmaade til fremstilling af l-sulpirid
WO2007038277A2 (fr)	2007-04-05	Resolution de derives d'acide alpha-(phenoxy) phenylacetique avec des naphtyl-alkylamines
KR100472609B1 (ko)	2005-07-07	레보부피바카인과그의유사체의결정화벙법
EP2118061B1 (fr)	2016-03-09	Procédé de résolution énantiomérique de d,l-(+)-thréo-méthylphénidate
JP4000113B2 (ja)	2007-10-31	（３ｓ）−３−メトキシカルボニル−４−フェニル酪酸金属塩およびその使用方法
WO2021166934A1 (fr)	2021-08-26	Procédé de fabrication de composé pyrrolidine
EP1341762A1 (fr)	2003-09-10	Procede de dissolution de melanges racemiques de derives de piperidine
CN111302996A (zh)	2020-06-19	一种高手性纯度的富马酸氯马斯汀的制备方法
US20200131126A1 (en)	2020-04-30	Process for the Separation of Optical Isomers of Racemic 3-Alkylpiperidine-Carboxylic Acid Ethyl Esters
TW202535846A (zh)	2025-09-16	製備（３ｒ）－氟吡咯啶鹽酸鹽之新方法
US20040039206A1 (en)	2004-02-26	Process for resolving racemic mixtures of piperidine derivatives
CN117510398A (zh)	2024-02-06	一种高光学纯度(3r,4r)/(3s,4s)-n-boc-4-氨基-3-羟基哌啶的制备方法
WO2010079605A1 (fr)	2010-07-15	Procédé de production de la 1-benzyl-3-aminopyrrolidine de pureté élevée
WO2000039090A1 (fr)	2000-07-06	Procede de preparation d'acetate de paroxetine et de ses analogues
WO2000039121A1 (fr)	2000-07-06	Procede de preparation d'un acetate de paroxetine ou d'analogues de paroxetine
EP1140912A1 (fr)	2001-10-10	Procede de preparation d'un sel d'acetate de paroxetine ou d'analogues de paroxetine