KR910019966A - 시마테롤의 거울상이성체의 분리, (-)-시마테롤 및 약학 조성물 또는 능률 증진제로서 이들의 용도 - Google Patents
시마테롤의 거울상이성체의 분리, (-)-시마테롤 및 약학 조성물 또는 능률 증진제로서 이들의 용도 Download PDFInfo
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- tartaric acid
- isopropylamino
- cyano
- phenyl
- ethanol
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- A23K20/10—Organic substances
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
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- A23K50/00—Feeding-stuffs specially adapted for particular animals
- A23K50/30—Feeding-stuffs specially adapted for particular animals for swines
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- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/275—Nitriles; Isonitriles
- A61K31/277—Nitriles; Isonitriles having a ring, e.g. verapamil
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/06—Antiasthmatics
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/02—Drugs for disorders of the urinary system of urine or of the urinary tract, e.g. urine acidifiers
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P21/00—Drugs for disorders of the muscular or neuromuscular system
- A61P21/02—Muscle relaxants, e.g. for tetanus or cramps
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- 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
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/04—Anorexiants; Antiobesity agents
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/08—Antiallergic agents
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C255/00—Carboxylic acid nitriles
- C07C255/49—Carboxylic acid nitriles having cyano groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
- C07C255/58—Carboxylic acid nitriles having cyano groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton containing cyano groups and singly-bound nitrogen atoms, not being further bound to other hetero atoms, bound to the carbon skeleton
- C07C255/59—Carboxylic acid nitriles having cyano groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton containing cyano groups and singly-bound nitrogen atoms, not being further bound to other hetero atoms, bound to the carbon skeleton the carbon skeleton being further substituted by singly-bound oxygen atoms
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- Animal Behavior & Ethology (AREA)
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- Chemical Kinetics & Catalysis (AREA)
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- Pulmonology (AREA)
- Food Science & Technology (AREA)
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- Neurology (AREA)
- Obesity (AREA)
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- Orthopedic Medicine & Surgery (AREA)
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- Urology & Nephrology (AREA)
- Neurosurgery (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
내용 없음
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (18)
- (-)-1-(4′-아미노-3′-시아노-페닐)-2-이소프로필아미노-에탄올 및 이의 산부가염.
- 제1항에 있어서, 본질상 광학적으로 순수한 것임을 특징으로 하는 화합물.
- 제1항에 있어서, 적어도 ee=90%의 광학적 순도를 가짐을 특징으로 하는 화합물.
- 제1항에 있어서, 적어도 ee=94%의 광학적 순도를 가짐을 특징으로 하는 화합물.
- 제1내지 4항중 적어도 한 항에 따른 화합물의 생릭적으로 허용되는 산부가염.
- 임의로 하나이상의 불활성 담체 및/또는 희석제와 함께 제1내지 4항중 적어도 한 항에 따른 화합물 또는 제5항에 따른 생리적으로 허용되는 산부가염을 함유하는 약학 조성물.
- 비만증, 폐색성 폐 변화, 알레르기성 기관지 천식, 경련성 기관지염, 염증 또는 조산을 치료하는데 적합한 약학 조성물을 제조하는데 제 1내지 5항중 적어도 한 항에 따른 화합물을 사용하는 용도.
- 제 1내지 5항중 적어도 한 항에 따른 화합물을 비-회학적 방법에 의해 하나이상의 불활성 담체 및/또는 희석제에 혼입함을 특징으로 하는 제6항에 따른 약학 조성물을 제조하는 방법.
- 동물의 능률 증진제로서 제 1내지 5항중 적어도 한 항에 따른 화합물을 사용하는 용도
- 제 1내지 5항중 적어도 한 항에 따른 화합물을 함유하는, 동물사료제조용 도물 사료 및 전혼합물.
- 제 1내지 5항중 적어도 한 항에 따른 화합물을 함유하는 동물에 대한 능률 증진제.
- 제 1내지 5항중 적어도 한 항에 따른 화합물을 증량제, 희석제와 영양제 및 임의로 다른 애주번트와 혼합함을 특징으로 하여, 동물에 대한 능률 증진제를 제조하는 방법.
- 1-(4′-아미노-3′-시아노-페닐)-2-이소프로필아미노-에탄올과 적어도 2당량의 광학적으로 활성적인 이염기성 보조산, 예컨대 (-)-0,0′-디벤조일-L-타르타르산,(+)-0,0′-디벤조일-D-타르타르산,(-)-0,0′-디톨릴-L-타르타르산 또는 (+)-0,0′-디톨릴-D-타르타르산을 각각의 보조산에 특징적인 온도범위 아래로 온도가 내려가지 않도록 하면서 적합한 용매에 용해시켜 1-(4′-아미노-3′-시아노-페닐)-2-이소프로필아미노-에탄올을 결정시키고 결정된 부분 입체 이성체염을 분리시킨 후 거울상 이성체 염기를 유리시키고 필요에 따라 이렇게 수득된 거울상 이성체 염기를 이의 생리적으로 허용되는 산부가염으로 전환시킴을 특징으로 하여, (-)-1-(4′-아미노-3′-시아노-페닐)-2-이소프로필아미노-에탄올과 (+)-1(4′-아미노-3′-시아노-페닐)-2-이소프로필아미노-에탄올을 제조하는 방법.
- 제13항에 있어서, 보조산으로서 (+)-0,0′-디벤조일-L-타르타르산을 25℃이상의 온도에서 사용함을 특징으로 하는 방법.
- 1-(4′-아미노-3′-시아노-페닐)-2-이소프로필아미노-에탄올과 광학적으로 활성적인 이염기성 보조산, 예컨대 (-)-0,0′-디벤조일-L-타르타르산 또는 (+)-0,0′-디벤조일-D-타르타르산, (-)-0,0′-디톨릴-L-타르타르산 또는 (+)-0,0-디톨릴-D-타르타르산의 부분 입체 이성체 염.
- (-)-1-(4′-아미노-3′-시아노-페닐)-2-이소프로필아미노-에탄올-(+)-0,0′-디벤조일-D-타르타르산 수소염
- 1-(4′-아미노-3′-시아노-페닐)-2-이소프로필아미노-에탄올과 적어도 2당량의 광학적으로 활성적인 이염기성 보조산, 예컨대 (-)-0,0′-디벤조일-L-타르타르산 (+)-0,0′-디벤조일-D-타르타르산, (-)-0,0′-디톨릴-L-타르타르산 또는 (+)-0,0-디톨릴-D-타르타르산을 각각의 보조산에 특징적인 온도범위 이하로 온도가 내려가지 않도록 하면서 적합한 용매에 용해시켜 1-(4′-아미노-3′-시아노-페닐)-2-이소프로필아미노-에탄올을 결정시킨후, 결정된 부분입체 이성체염을 분리함을 특징으로 하여, 제15항 또는 제16항에 따른 부붑 입체 이성체염을 제조하는 방법.
- 제13항 또는 제17항에 있어서, 20℃이상, 바람직하게는 25내지 30℃에서 결정화 과정을 수행함을 특징으로 하는 방법.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DEP4014252.3 | 1990-05-04 | ||
DE4014252A DE4014252A1 (de) | 1990-05-04 | 1990-05-04 | Enantiomerentrennung von cimaterol, (-)-cimaterol und dessen verwendung als arzneimittel oder als leistungsfoerderer |
Publications (2)
Publication Number | Publication Date |
---|---|
KR910019966A true KR910019966A (ko) | 1991-12-19 |
KR0183024B1 KR0183024B1 (ko) | 1999-05-15 |
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Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019910007085A KR0183024B1 (ko) | 1990-05-04 | 1991-05-02 | 시마테롤의 거울상이성체의 분리, (-)-시마테롤 및 약학 조성물 또는 능률 증진제로서 이들의 용도 |
Country Status (27)
Country | Link |
---|---|
US (4) | US5248695A (ko) |
EP (2) | EP0455155B1 (ko) |
JP (1) | JP2944777B2 (ko) |
KR (1) | KR0183024B1 (ko) |
AR (1) | AR247728A1 (ko) |
AT (2) | ATE124932T1 (ko) |
AU (1) | AU645313B2 (ko) |
BG (1) | BG60743B1 (ko) |
CA (1) | CA2041818C (ko) |
CZ (1) | CZ286389B6 (ko) |
DE (3) | DE4014252A1 (ko) |
DK (2) | DK0455155T3 (ko) |
ES (2) | ES2075255T3 (ko) |
FI (1) | FI109600B (ko) |
GR (2) | GR3017064T3 (ko) |
HU (1) | HU214335B (ko) |
ID (1) | ID966B (ko) |
IE (2) | IE69017B1 (ko) |
IL (1) | IL98030A (ko) |
NO (1) | NO174803B (ko) |
NZ (1) | NZ238032A (ko) |
PT (1) | PT97544B (ko) |
RU (1) | RU2002737C1 (ko) |
SG (1) | SG45439A1 (ko) |
SK (1) | SK279258B6 (ko) |
TW (1) | TW197415B (ko) |
ZA (1) | ZA913337B (ko) |
Families Citing this family (17)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE4014252A1 (de) * | 1990-05-04 | 1991-11-07 | Boehringer Ingelheim Vetmed | Enantiomerentrennung von cimaterol, (-)-cimaterol und dessen verwendung als arzneimittel oder als leistungsfoerderer |
GB2289842B (en) * | 1991-04-05 | 1996-01-31 | Sepracor Inc | Improved use of ß2 bronchodilator drugs |
GB9107196D0 (en) * | 1991-04-05 | 1991-05-22 | Sandoz Ag | Improvements in or relating to organic compounds |
CA2247953A1 (en) * | 1996-01-29 | 1997-07-31 | E. Charles Pesterfield Jr. | Method of treating undesired uterine contractions using optically pure r- or rr-isomers of adrenergic beta-2 agonists |
EP1787529A3 (en) * | 1997-04-30 | 2009-11-18 | Courage Corporation Pty Ltd. | Composition and methods using an eutomer |
BR9815470A (pt) | 1997-04-30 | 2001-10-23 | Bridge Pharma Inc | Composição e processo usando um eutÈmero |
ZA994264B (en) | 1998-07-01 | 2000-01-25 | Warner Lambert Co | Stereoisomers with high affinity for adrenergic receptors. |
US7232837B2 (en) | 1999-06-29 | 2007-06-19 | Mcneil-Ppc, Inc. | Stereoisomers with high affinity for adrenergic receptors |
HUP0300832A2 (hu) * | 2000-04-27 | 2003-08-28 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Új, lassú hatású bétamimetikumok, eljárás előállításukra és alkalmazásuk és ezeket tartalmazó gyógyszerkészítmények |
US20030162459A1 (en) * | 2002-02-27 | 2003-08-28 | Osbon Robert Lindsay | Method for producing a nonwoven fabric with enhanced characteristics |
US20040235922A1 (en) * | 2003-05-15 | 2004-11-25 | Baile Clifton A. | Compositions and methods for inducing adipose tissue cell death |
SI1663197T1 (sl) * | 2003-09-09 | 2008-06-30 | Biogen Idec Internat Gmbh | Uporaba derivatov fumarne kisline za zdravljenje sräśne insuficience in astme |
SG124283A1 (en) * | 2004-03-24 | 2006-08-30 | Trusted Hub Ltd | Document signature method & system |
PL1719507T3 (pl) | 2005-04-13 | 2010-12-31 | Cipher Pharmaceuticals Inc | Agoniści receptora beta2-adrenergicznego do leczenia chorób tkanki łącznej skóry |
US20090181369A1 (en) * | 2005-05-27 | 2009-07-16 | George Q Daley | Methods for the Treatment of Disease |
US20090305225A1 (en) * | 2005-06-13 | 2009-12-10 | Galbraith Richard A | Inhibition of Creatine Uptake to Promote Weight Loss |
DK2925725T3 (en) | 2012-12-03 | 2017-01-16 | Pfizer | androgen receptor modulators |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
NL136601C (ko) * | 1967-06-15 | |||
US4119710A (en) * | 1972-12-18 | 1978-10-10 | Boehringer Ingelheim Gmbh | Bronchospasmolytic 1-(p-amino-phenyl)-2-amino-ethanols-(1) and salts |
US4407819A (en) * | 1980-08-25 | 1983-10-04 | American Cyanamid Company | Phenylethanolamine derivatives and acid addition salts thereof for the depression of fat deposition in warm blooded animals |
US4814350A (en) * | 1986-09-10 | 1989-03-21 | American Cyanamid Company | Method of treating diabetes with 5-[1-hydroxy-2-(isopropylamino)ethyl]anthranilonitrile |
US4792546A (en) * | 1986-12-05 | 1988-12-20 | American Cyanamid Company | Method for increasing weight gains and reducing deposition of fat in animals |
DE4014252A1 (de) * | 1990-05-04 | 1991-11-07 | Boehringer Ingelheim Vetmed | Enantiomerentrennung von cimaterol, (-)-cimaterol und dessen verwendung als arzneimittel oder als leistungsfoerderer |
-
1990
- 1990-05-04 DE DE4014252A patent/DE4014252A1/de not_active Withdrawn
-
1991
- 1991-04-26 DE DE59105957T patent/DE59105957D1/de not_active Expired - Fee Related
- 1991-04-26 ES ES91106774T patent/ES2075255T3/es not_active Expired - Lifetime
- 1991-04-26 ES ES93117935T patent/ES2109412T3/es not_active Expired - Lifetime
- 1991-04-26 SG SG1996008586A patent/SG45439A1/en unknown
- 1991-04-26 DK DK91106774.2T patent/DK0455155T3/da active
- 1991-04-26 AT AT91106774T patent/ATE124932T1/de not_active IP Right Cessation
- 1991-04-26 AT AT93117935T patent/ATE158277T1/de not_active IP Right Cessation
- 1991-04-26 DK DK93117935.2T patent/DK0589488T3/da active
- 1991-04-26 EP EP91106774A patent/EP0455155B1/de not_active Expired - Lifetime
- 1991-04-26 DE DE59108853T patent/DE59108853D1/de not_active Expired - Fee Related
- 1991-04-26 EP EP93117935A patent/EP0589488B1/de not_active Expired - Lifetime
- 1991-04-29 AU AU76111/91A patent/AU645313B2/en not_active Ceased
- 1991-04-30 US US07/693,760 patent/US5248695A/en not_active Expired - Fee Related
- 1991-05-01 TW TW080103440A patent/TW197415B/zh active
- 1991-05-02 IL IL9803091A patent/IL98030A/en not_active IP Right Cessation
- 1991-05-02 KR KR1019910007085A patent/KR0183024B1/ko not_active IP Right Cessation
- 1991-05-02 PT PT97544A patent/PT97544B/pt not_active IP Right Cessation
- 1991-05-02 JP JP3100832A patent/JP2944777B2/ja not_active Expired - Fee Related
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- 1991-05-03 FI FI912151A patent/FI109600B/fi not_active IP Right Cessation
- 1991-05-03 CZ CS19911292A patent/CZ286389B6/cs not_active IP Right Cessation
- 1991-05-03 ZA ZA913337A patent/ZA913337B/xx unknown
- 1991-05-03 IE IE150791A patent/IE69017B1/en not_active IP Right Cessation
- 1991-05-03 BG BG94342A patent/BG60743B1/bg not_active Expired - Lifetime
- 1991-05-03 SK SK1292-91A patent/SK279258B6/sk unknown
- 1991-05-03 AR AR91319603A patent/AR247728A1/es not_active Expired - Lifetime
- 1991-05-03 CA CA002041818A patent/CA2041818C/en not_active Expired - Fee Related
- 1991-05-03 HU HU911502A patent/HU214335B/hu not_active IP Right Cessation
- 1991-05-03 NZ NZ238032A patent/NZ238032A/en unknown
- 1991-05-03 IE IE950792A patent/IE80651B1/en not_active IP Right Cessation
- 1991-12-18 RU SU915010409A patent/RU2002737C1/ru not_active IP Right Cessation
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1992
- 1992-01-31 ID IDP198592A patent/ID966B/id unknown
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1993
- 1993-06-23 US US08/081,996 patent/US5292753A/en not_active Expired - Fee Related
- 1993-12-14 US US08/166,584 patent/US5395957A/en not_active Expired - Lifetime
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1994
- 1994-11-29 US US08/346,105 patent/US5648386A/en not_active Expired - Fee Related
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1995
- 1995-08-09 GR GR950402190T patent/GR3017064T3/el unknown
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1997
- 1997-12-02 GR GR970403196T patent/GR3025547T3/el unknown
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