KR870007118A - 광학적으로 순수한 화합물 및 그의 제조 방법 - Google Patents
광학적으로 순수한 화합물 및 그의 제조 방법 Download PDFInfo
- Publication number
- KR870007118A KR870007118A KR860011720A KR860011720A KR870007118A KR 870007118 A KR870007118 A KR 870007118A KR 860011720 A KR860011720 A KR 860011720A KR 860011720 A KR860011720 A KR 860011720A KR 870007118 A KR870007118 A KR 870007118A
- Authority
- KR
- South Korea
- Prior art keywords
- propyl
- hydrochloride
- weight
- water
- volume
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title claims 7
- 238000002360 preparation method Methods 0.000 title 1
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims 6
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 5
- 238000002690 local anesthesia Methods 0.000 claims 3
- 230000003444 anaesthetic effect Effects 0.000 claims 2
- 230000001939 inductive effect Effects 0.000 claims 2
- 239000003589 local anesthetic agent Substances 0.000 claims 2
- 238000000034 method Methods 0.000 claims 2
- 150000004682 monohydrates Chemical group 0.000 claims 2
- 241000124008 Mammalia Species 0.000 claims 1
- 238000009835 boiling Methods 0.000 claims 1
- 239000012467 final product Substances 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- 239000000825 pharmaceutical preparation Substances 0.000 claims 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
-
- 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)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Abstract
내용 없음
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (10)
- 일수화물 형태임을 특징으로 하는 S-(-)-1-프로필-2',6'-피페콜옥실리디드 염산염.
- 제1항에 있어서, 실제로 광학적으로 순수함을 특징으로 하는 화합물.
- 제1항에 있어서, 대응하는 R-(+)-에난티오머를 0.5중량%미만 함유량을 특징으로하는 화합물.
- S-(-)-1-프로필-2',6'-피페콜옥실리디드 염산염을 물 중에 용해시키고, 여기에 45℃내지 비점 온도까지 가열시킨 아세톤을 첨가한 후, S-(-)-1-프로필-2',6'-피페콜옥실리디드 염산염의 일 수화물을 단리시킴을 특징으로 하는, 실제로 광학적으로 순수한 S-(-)-1-프로필 2',6'-피페콜옥실리디드 염산염의 제조 방법.
- 제4항에 있어서, S-(-)-1-프로필-2',6'-피페콜옥실리디드 염산염을 그의 중량의 1-3배에 해당하는 양의 물 중에 용해시키고, 여기에 아세톤을 물 용적의 5-15배 용적으로 첨가한 후, 용액을 여과시키고, 최종 생성물을 단리시킴을 특징으로 하는 방법.
- 제5항에 있어서, 물의 중량을 S-(-)-1-프로필-2',6'-피페콜옥실리디드 염산염의 중량과 동량으로하고, 아세톤의 용적을 첨가한 물 용적의 10배로 함을 특징으로 하는 방법.
- 제1항에 의한 화합물을 함유함을 특징으로 하는 국부 마취용 약제.
- 국부 마취 유도 용도의 제1항에 의한 화합물.
- 국부 마취를 필요로 하는 인체를 포함한 포유 동물에 제1항에 의한 화합물을 마취량으로 투여하는것으로 되는, 국부 마취 유도 방법.
- 제1항에 의한 화합물의 국부 마취 효과를 갖는 약제 제조 용도.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (2)
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 |
SE8600017-1 | 1986-01-03 |
Publications (2)
Publication Number | Publication Date |
---|---|
KR870007118A true KR870007118A (ko) | 1987-08-14 |
KR940008302B1 KR940008302B1 (ko) | 1994-09-12 |
Family
ID=20363001
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019860011720A KR940008302B1 (ko) | 1986-01-03 | 1986-12-31 | 광학적으로 순수한 s-(-)-1-프로필-2',6'-피페콜옥실리디드 염산염의 제조방법 |
Country Status (29)
Country | Link |
---|---|
US (1) | US4870086A (ko) |
EP (1) | EP0239710B1 (ko) |
JP (1) | JPH07598B2 (ko) |
KR (1) | KR940008302B1 (ko) |
AR (1) | AR242561A1 (ko) |
AT (1) | ATE56956T1 (ko) |
AU (1) | AU592392B2 (ko) |
BG (1) | BG62066B2 (ko) |
CA (1) | CA1276154C (ko) |
CY (1) | CY1680A (ko) |
DE (1) | DE3674582D1 (ko) |
DK (1) | DK171378B1 (ko) |
EG (1) | EG17867A (ko) |
ES (1) | ES2036179T3 (ko) |
FI (1) | FI83075C (ko) |
GR (1) | GR3002516T3 (ko) |
HK (1) | HK5493A (ko) |
IE (1) | IE59061B1 (ko) |
LU (1) | LU88843I2 (ko) |
LV (1) | LV5765B4 (ko) |
MY (1) | MY101132A (ko) |
NL (1) | NL960005I2 (ko) |
NO (2) | NO170330C (ko) |
NZ (1) | NZ218615A (ko) |
PH (1) | PH22924A (ko) |
PT (1) | PT84041B (ko) |
SE (1) | SE451840B (ko) |
SG (1) | SG117292G (ko) |
ZA (1) | ZA868600B (ko) |
Families Citing this family (17)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
SI21560B (sl) * | 1990-06-07 | 2005-04-30 | Astrazeneca Ab | 3,5-disubstituirani indolni derivati kot "5-HT1-podobni" receptorski agonisti |
ES2082703B1 (es) * | 1993-11-04 | 1996-12-16 | Inst Investigacion Desarrollo | Nuevos derivados de ciclopropilo, procedimientos para su preparacion y aplicaciones. |
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 |
AU695479B2 (en) * | 1994-09-23 | 1998-08-13 | Darwin Discovery Limited | Racemisation and asymmetric transformation processes used in the manufacture of levobupivacaine and analogues thereof |
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 |
WO2007123405A1 (en) * | 2006-04-25 | 2007-11-01 | Dishman Pharmaceuticals And Chemicals Ltd. | Ropivacaine hydrochloride anhydrate and the preparation thereof |
DK2234974T3 (da) * | 2008-01-15 | 2012-06-25 | Pharmathen Sa | Fremgangsmåde til fremstilling af (S)-1-alkyl-2',6'-pipecoloxylidid-forbindelse |
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 |
US9320908B2 (en) | 2009-01-15 | 2016-04-26 | Autonomic Technologies, Inc. | Approval per use implanted neurostimulator |
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 |
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 |
US2799679A (en) * | 1955-04-28 | 1957-07-16 | Bofors Ab | Process of preparing amides of heterocyclic carboxylic acids |
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 |
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 (ko) * | 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 |
WO1985000599A1 (en) * | 1983-08-01 | 1985-02-14 | A/S Apothekernes Laboratorium For Specialpraeparat | L-N-n-PROPYLPIPECOLIC ACID-2,6-XYLIDIDE AND METHOD FOR PREPARING THE SAME |
-
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 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
- 1986-12-15 EP EP86850440A patent/EP0239710B1/en not_active Expired - Lifetime
- 1986-12-15 ES ES198686850440T patent/ES2036179T3/es not_active Expired - Lifetime
- 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/en not_active Expired - Lifetime
- 1986-12-31 PT PT84041A patent/PT84041B/pt unknown
- 1986-12-31 KR KR1019860011720A patent/KR940008302B1/ko not_active IP Right Cessation
-
1987
- 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
- 1987-01-02 FI FI870003A patent/FI83075C/fi 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/xx not_active IP Right Cessation
- 1993-10-10 CY CY1680A patent/CY1680A/xx unknown
-
1994
- 1994-02-18 BG BG98494A 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
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