KR840007554A - 결정성 이부프로펜의 제조방법 - Google Patents
결정성 이부프로펜의 제조방법 Download PDFInfo
- Publication number
- KR840007554A KR840007554A KR1019840000801A KR840000801A KR840007554A KR 840007554 A KR840007554 A KR 840007554A KR 1019840000801 A KR1019840000801 A KR 1019840000801A KR 840000801 A KR840000801 A KR 840000801A KR 840007554 A KR840007554 A KR 840007554A
- Authority
- KR
- South Korea
- Prior art keywords
- ibuprofen
- solvent
- liquid
- mixture
- solution
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C57/00—Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms
- C07C57/30—Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms containing six-membered aromatic rings
-
- 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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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pain & Pain Management (AREA)
- Pharmacology & Pharmacy (AREA)
- Rheumatology (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Medicinal Preparation (AREA)
Abstract
내용 없음.
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
제1도는 온도에 대한 각종 용매중에서 용해도를 나타낸 그래프이다.
Claims (11)
- 약 20-60℃ 온도에서 이부프로펜을 적어도 약 10용량%의 δH8 액체 용매를 함유하는 액체용매에 용해시켜 용액을 생성한 후; 이부프로펜:δH8 용매용액의 온도를 그안에 함유된 이부프로펜 성분이 실질적으로 완전히 용해된 용액으로 되게하기 위해 포화점까지 필요한 만큼 조절하고; 결과 생성된 δH8 용매중 이부프로펜 용액을 약 0-3시간에 걸쳐 0∼-20℃로 냉각하여 이 용액으로부터 이부프로펜이 결정화되고 침전되게 한 후; 냉각된 이부프로펜:δH8 용매혼합물을 충분한 시간동안 진탕하여 혼합물중 고체/액체 평형 상태를 얻은 후; 혼합물의 액체 성분으로 부터 결정성 이부프로펜을 분리하는 것으로 구성된 결정성 이부프로펜의 제조방법.
- 제1항에 있어서, 이부프로펜의 δH8 액체 혼합물중 과포하 용액을 고체 이부프로펜으로 접종하여 뒤이은 냉각 조작중에 결정화가 유발되게 하는 방법.
- 제1항에 있어서 δH8 용매성분을 메탄올, 에탄올, 이소프로판올 및 그 혼합물로 구성된 군으로부터 선택하는 방법.
- 제2항에 있어서 결과 생성된 이부프로펜/δH8 용매 액체 혼합물에 이부프로펜의 용해도를 감소시키는 액체를 혼합하는 단계를 더 포함하여 결과 생성된 혼합물로부터 이부프로펜의 결정화 및 침전이 일어나게 하는 방법.
- 제4항에 있어서 이부프로펜/δH8 액체와 혼합되는 용해도 감소액체가 물, 헥산, 헵탄, 톨루엔, 초산에틸, 에틸렌글리콜, 프로필렌글리콜, 글리세린 및 그 혼합물로 구성된 군으로부터 선택되는 방법.
- 제1항에 있어서 결정화될 이부프로펜이 δH8 용매성분과 비-C1-C3용매 성분의 액체 용매 혼합물중에 함유되어 있으며 여기서 비-δH8 용매 액체 성분은 극성이 적으며 C1-C3-알카놀 보다 이부프로펜에 대한 수소결합 능력이 적은 방법.
- 제6항에 있어서 δH8 용매 액체 성분이 C1-C3-알카놀인 방법.
- 제1항에 있어서 결정화될 이부프로펜이 용매액체 혼합물중 물을 90%까지 함유하는 δH8 용매 액체/물 혼합물인 방법.
- 제8항에 있어서 δH8 용매액체 성분이 C1-C3-알카놀인 방법.
- 이부프로펜을 수소결합매개변수[δH]가 약 8힐데브란드 단위보다 큰 액체 용매중의 그의 용액으로부터 결정화하는 것으로 구성된 실질적으로 등방정 또는 육방정 형상의 결정습성을 가진 이부프로펜을 제조하는 방법.
- 제1항에 있어서 이부프로펜을 약 10용량%의 물을 함유하는 에탄올 용액으로 구성된 용매 혼합물로부터 결정화하는 방법.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US47082083A | 1983-02-28 | 1983-02-28 | |
US470820 | 1983-02-28 | ||
US06/517,116 US4476248A (en) | 1983-02-28 | 1983-07-25 | Crystallization of ibuprofen |
US517116 | 1983-07-25 |
Publications (2)
Publication Number | Publication Date |
---|---|
KR840007554A true KR840007554A (ko) | 1984-12-08 |
KR900003298B1 KR900003298B1 (ko) | 1990-05-14 |
Family
ID=27043233
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019840000801A KR900003298B1 (ko) | 1983-02-28 | 1984-02-20 | 결정성 이부프로펜의 제조방법 |
Country Status (10)
Country | Link |
---|---|
US (1) | US4476248A (ko) |
EP (1) | EP0120587B1 (ko) |
JP (1) | JPH0623126B2 (ko) |
KR (1) | KR900003298B1 (ko) |
AU (1) | AU567125B2 (ko) |
CA (1) | CA1212693A (ko) |
DE (1) | DE3460098D1 (ko) |
ES (1) | ES530082A0 (ko) |
MX (1) | MX161333A (ko) |
PH (1) | PH20032A (ko) |
Families Citing this family (41)
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GB8606762D0 (en) * | 1986-03-19 | 1986-04-23 | Boots Co Plc | Therapeutic agents |
US5015646A (en) * | 1987-08-28 | 1991-05-14 | Bristol-Myers Squibb Co. | Pharmaceutically useful polymorphic modification of buspirone |
US4810789A (en) * | 1987-08-28 | 1989-03-07 | Bristol-Myers Company | Process for buspirone hydrochloride polymorphic crystalline form conversion |
SE463541B (sv) | 1987-08-31 | 1990-12-10 | Lejus Medical Ab | Granulaer produkt oeverdragen av en smaelta av sig sjaelv samt foerfarande foer dess framstaellning |
ATE121619T1 (de) * | 1990-04-11 | 1995-05-15 | Upjohn Co | Verfahren zum geschmacksabdecken von ibuprofen. |
US5151551A (en) * | 1990-09-06 | 1992-09-29 | Hoechst Celanese Corporation | Method for purification of ibuprofen comprising mixtures |
WO1992008686A1 (en) * | 1990-11-19 | 1992-05-29 | Ethyl Corporation | Process for improving flow characteristics of crystalline ibuprofen |
US5191114A (en) * | 1991-10-09 | 1993-03-02 | Sage Pharmaceuticals, Inc. | Process for enhancing the flow characteristics of ibuprofen |
US5300301A (en) * | 1992-12-02 | 1994-04-05 | Hoechst Celanese Corporation | Isolation of ibuprofen from tablets |
AT401871B (de) * | 1994-01-28 | 1996-12-27 | Gebro Broschek Gmbh | Verfahren zur herstellung von s(+)-ibuprofen- partikeln mit verbesserten fliesseigenschaften und deren verwendung zur arzneimittelherstellung |
US5608048A (en) * | 1995-06-05 | 1997-03-04 | Bristol-Myers Squibb Company | d4 T polymorphic Form 1 process |
US5922695A (en) * | 1996-07-26 | 1999-07-13 | Gilead Sciences, Inc. | Antiviral phosphonomethyoxy nucleotide analogs having increased oral bioavarilability |
GB2315661B (en) * | 1996-07-26 | 2000-05-03 | Unilever Plc | Frozen food product |
TR199902202T2 (xx) * | 1997-03-14 | 1999-12-21 | Unilever N.V. | Dondurulmu� g�da �r�n�. |
US5935946A (en) * | 1997-07-25 | 1999-08-10 | Gilead Sciences, Inc. | Nucleotide analog composition and synthesis method |
ZA986614B (en) | 1997-07-25 | 1999-01-27 | Gilead Sciences | Nucleotide analog composition |
FI122018B (fi) * | 2000-01-31 | 2011-07-29 | Danisco | Menetelmä betaiinin kiteyttämiseksi |
HRP20000328A2 (en) * | 2000-05-19 | 2002-02-28 | Pliva Farmaceutska Ind Dionik | Novel polymorph v of torasemide |
CA2788498C (en) * | 2001-03-01 | 2016-02-16 | Gilead Sciences, Inc. | Polymorphic and other crystalline forms of cis-ftc |
PL367262A1 (en) * | 2001-04-26 | 2005-02-21 | Bristol-Myers Squibb Company | A pharmaceutical tablet having a high api content |
DE10153934A1 (de) * | 2001-11-06 | 2003-05-22 | Basf Ag | Verfahren zur Kristallisation von Profenen |
DE602004014470D1 (de) | 2003-01-14 | 2008-07-31 | Gilead Sciences Inc | Zusammensetzungen und verfahren zur antiviralen kombinationstherapie |
ATE442352T1 (de) * | 2003-05-16 | 2009-09-15 | Cephalon France | Verfahren zur herstellung von modafinil |
FR2857253B1 (fr) * | 2003-07-07 | 2007-02-09 | Ethypharm Sa | Installation comprenant une machine de fabrication de comprimes en particulier a usage therapeuthique |
US20050137262A1 (en) * | 2003-12-22 | 2005-06-23 | Hu Patrick C. | Highly concentrated pourable aqueous solutions of potassium ibuprofen, their preparation and their uses |
US20080247582A1 (en) | 2004-09-09 | 2008-10-09 | Guenther Godehard A | Loudspeaker and Systems |
TWI375560B (en) | 2005-06-13 | 2012-11-01 | Gilead Sciences Inc | Composition comprising dry granulated emtricitabine and tenofovir df and method for making the same |
TWI471145B (zh) | 2005-06-13 | 2015-02-01 | Bristol Myers Squibb & Gilead Sciences Llc | 單一式藥學劑量型 |
CL2007002425A1 (es) * | 2006-08-22 | 2008-06-27 | Albermarle Corp | Procedimiento de preparacion controlado de sal sodica de ibuprofeno de tamano de particula mediano; y dichas particulas de sal sodica. |
US8189840B2 (en) | 2007-05-23 | 2012-05-29 | Soundmatters International, Inc. | Loudspeaker and electronic devices incorporating same |
JP2011500724A (ja) * | 2007-10-19 | 2011-01-06 | パーデュ リサーチ ファンデーション | 結晶性化合物の固体製剤 |
EP2445486B1 (en) * | 2009-06-22 | 2017-11-08 | Wyeth LLC | Sodium ibuprofen tablets and methods of manufacturing pharmaceutical compositions including sodium ibuprofen |
CN103221391B (zh) | 2010-01-27 | 2018-07-06 | 艾尼纳制药公司 | (R)-2-(7-(4-环戊基-3-(三氟甲基)苄基氧基)-1,2,3,4-四氢环戊二烯并[b]吲哚-3-基)乙酸及其盐的制备方法 |
JP5821247B2 (ja) * | 2010-04-07 | 2015-11-24 | 大正製薬株式会社 | イブプロフェンの昇華抑制方法 |
CN102311335B (zh) * | 2010-06-29 | 2013-12-11 | 山东新华制药股份有限公司 | 高松密度布洛芬的制备工艺 |
KR101324862B1 (ko) * | 2011-07-12 | 2013-11-01 | (주)에이에스텍 | 클로피도그렐 황산수소염의 구형 입자, 이를 포함하는 약학적 조성물 및 이의 제조방법 |
CN102936194A (zh) * | 2012-11-14 | 2013-02-20 | 陕西合成药业有限公司 | 一种高纯度的布洛芬的精制方法 |
US10301262B2 (en) | 2015-06-22 | 2019-05-28 | Arena Pharmaceuticals, Inc. | Crystalline L-arginine salt of (R)-2-(7-(4-cyclopentyl-3-(trifluoromethyl)benzyloxy)-1,2,3,4-tetrahydrocyclo-penta [b]indol-3-yl)acetic acid(Compund1) for use in SIPI receptor-associated disorders |
EP3582772A1 (en) | 2017-02-16 | 2019-12-25 | Arena Pharmaceuticals, Inc. | Compounds and methods for treatment of primary biliary cholangitis |
MA47503A (fr) | 2017-02-16 | 2021-04-21 | Arena Pharm Inc | Composés et méthodes pour le traitement de maladies inflammatoires chroniques de l'intestin avec manifestations extra-intestinales |
CN113200846B (zh) * | 2021-04-23 | 2022-04-22 | 浙江新和成股份有限公司 | 一种高松密度布洛芬球形晶体的制备方法及其产品 |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB971700A (en) * | 1961-02-02 | 1964-09-30 | Boots Pure Drug Co Ltd | Anti-Inflammatory Agents |
IT1059677B (it) * | 1974-03-22 | 1982-06-21 | Neopharmed Spa | Sale di lisina ad azione terapeutica |
JPS553336B2 (ko) * | 1974-04-11 | 1980-01-24 | ||
CA1062721A (en) * | 1975-12-15 | 1979-09-18 | Anthony A. Sinkula | Propionic acid derivatives |
US4189596A (en) * | 1976-05-24 | 1980-02-19 | The Upjohn Company | Preparing 2-arylalkanoic acid derivatives |
-
1983
- 1983-07-25 US US06/517,116 patent/US4476248A/en not_active Expired - Lifetime
-
1984
- 1984-01-10 CA CA000445027A patent/CA1212693A/en not_active Expired
- 1984-01-24 MX MX200133A patent/MX161333A/es unknown
- 1984-01-25 AU AU23771/84A patent/AU567125B2/en not_active Ceased
- 1984-02-17 EP EP84301050A patent/EP0120587B1/en not_active Expired
- 1984-02-17 DE DE8484301050T patent/DE3460098D1/de not_active Expired
- 1984-02-20 KR KR1019840000801A patent/KR900003298B1/ko not_active IP Right Cessation
- 1984-02-24 PH PH30294A patent/PH20032A/en unknown
- 1984-02-27 JP JP59037185A patent/JPH0623126B2/ja not_active Expired - Lifetime
- 1984-02-27 ES ES530082A patent/ES530082A0/es active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS59167536A (ja) | 1984-09-21 |
EP0120587A1 (en) | 1984-10-03 |
MX161333A (es) | 1990-09-10 |
ES8504658A1 (es) | 1985-05-01 |
AU2377184A (en) | 1984-09-06 |
CA1212693A (en) | 1986-10-14 |
AU567125B2 (en) | 1987-11-12 |
ES530082A0 (es) | 1985-05-01 |
JPH0623126B2 (ja) | 1994-03-30 |
PH20032A (en) | 1986-09-04 |
US4476248A (en) | 1984-10-09 |
DE3460098D1 (en) | 1986-05-28 |
KR900003298B1 (ko) | 1990-05-14 |
EP0120587B1 (en) | 1986-04-23 |
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