HUP0303526A2 - Azetidinon-intermedier vegyületek enantioszelektiv szintézise - Google Patents
Azetidinon-intermedier vegyületek enantioszelektiv szintéziseInfo
- Publication number
- HUP0303526A2 HUP0303526A2 HU0303526A HUP0303526A HUP0303526A2 HU P0303526 A2 HUP0303526 A2 HU P0303526A2 HU 0303526 A HU0303526 A HU 0303526A HU P0303526 A HUP0303526 A HU P0303526A HU P0303526 A2 HUP0303526 A2 HU P0303526A2
- Authority
- HU
- Hungary
- Prior art keywords
- intermediate compounds
- enantioselective synthesis
- azetidinone intermediate
- azetidinone
- enantioselective
- Prior art date
Links
- MNFORVFSTILPAW-UHFFFAOYSA-N azetidin-2-one Chemical compound O=C1CCN1 MNFORVFSTILPAW-UHFFFAOYSA-N 0.000 title abstract 2
- 150000001875 compounds Chemical class 0.000 title abstract 2
- 230000015572 biosynthetic process Effects 0.000 title 1
- 238000003786 synthesis reaction Methods 0.000 title 1
- HVYWMOMLDIMFJA-DPAQBDIFSA-N cholesterol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CCCC(C)C)[C@@]1(C)CC2 HVYWMOMLDIMFJA-DPAQBDIFSA-N 0.000 abstract 2
- 201000001320 Atherosclerosis Diseases 0.000 abstract 1
- 239000008280 blood Substances 0.000 abstract 1
- 210000004369 blood Anatomy 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 230000002265 prevention Effects 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
- C07D263/02—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
- C07D263/08—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
- C07D263/16—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member 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
- C07D263/18—Oxygen atoms
- C07D263/20—Oxygen atoms attached in position 2
- C07D263/22—Oxygen atoms attached in position 2 with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, directly attached to other ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
- C07D263/02—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
- C07D263/08—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
- C07D263/16—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member 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
- C07D263/18—Oxygen atoms
- C07D263/20—Oxygen atoms attached in position 2
- C07D263/26—Oxygen atoms attached in position 2 with hetero atoms or acyl radicals directly attached to the ring nitrogen atom
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Heart & Thoracic Surgery (AREA)
- General Health & Medical Sciences (AREA)
- Vascular Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Urology & Nephrology (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Cardiology (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Plural Heterocyclic Compounds (AREA)
- Steroid Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Catalysts (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
Abstract
A találmány tárgya eljárás az atherosclerosis kezelésére ésmegelőzésére alkalmazható, alacsony vérkoleszterinszintet eredményező,azetidinon vegyületek előállításában intermedierként szereplő képletűvegyület enantioszelektív előállítására. Ó
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US27928801P | 2001-03-28 | 2001-03-28 | |
US60/279,288 | 2001-03-28 | ||
PCT/US2002/009123 WO2002079174A2 (en) | 2001-03-28 | 2002-03-25 | Enantioselective synthesis of azetidinone intermediate compounds |
Publications (3)
Publication Number | Publication Date |
---|---|
HUP0303526A2 true HUP0303526A2 (hu) | 2004-01-28 |
HUP0303526A3 HUP0303526A3 (en) | 2004-11-29 |
HU230229B1 HU230229B1 (hu) | 2015-10-28 |
Family
ID=23068350
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
HU0303526A HU230229B1 (hu) | 2001-03-28 | 2002-03-25 | Azetidinon-intermedier vegyületek enantioszelektiv szintézise |
Country Status (29)
Country | Link |
---|---|
US (1) | US6627757B2 (hu) |
EP (1) | EP1373230B1 (hu) |
JP (1) | JP4145663B2 (hu) |
KR (1) | KR100590342B1 (hu) |
CN (1) | CN1275949C (hu) |
AT (1) | ATE305459T1 (hu) |
AU (1) | AU2002258605B2 (hu) |
BG (1) | BG66189B1 (hu) |
BR (1) | BRPI0208384B1 (hu) |
CA (1) | CA2442219C (hu) |
CZ (1) | CZ304929B6 (hu) |
DE (1) | DE60206365T2 (hu) |
DK (1) | DK1373230T3 (hu) |
EA (1) | EA006898B1 (hu) |
EE (1) | EE05453B1 (hu) |
ES (1) | ES2245733T3 (hu) |
HK (1) | HK1057546A1 (hu) |
HR (1) | HRP20030760B1 (hu) |
HU (1) | HU230229B1 (hu) |
IL (2) | IL157552A0 (hu) |
MX (1) | MXPA03008803A (hu) |
NZ (1) | NZ527852A (hu) |
PL (1) | PL205952B1 (hu) |
RS (1) | RS50386B (hu) |
SI (1) | SI1373230T1 (hu) |
SK (1) | SK287408B6 (hu) |
UA (1) | UA75644C2 (hu) |
WO (1) | WO2002079174A2 (hu) |
ZA (1) | ZA200306612B (hu) |
Families Citing this family (35)
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GB0215579D0 (en) | 2002-07-05 | 2002-08-14 | Astrazeneca Ab | Chemical compounds |
US20040132058A1 (en) | 2002-07-19 | 2004-07-08 | Schering Corporation | NPC1L1 (NPC3) and methods of use thereof |
US7135556B2 (en) * | 2002-07-19 | 2006-11-14 | Schering Corporation | NPC1L1 (NPC3) and methods of use thereof |
AR040588A1 (es) | 2002-07-26 | 2005-04-13 | Schering Corp | Formulacion farmaceutica que comprende un inhibidor de la absorcion del colesterol y un inhibidor de una hmg- co a reductasa |
EP1918000A2 (en) | 2003-11-05 | 2008-05-07 | Schering Corporation | Combinations of lipid modulating agents and substituted azetidinones and treatments for vascular conditions |
WO2005061452A1 (en) | 2003-12-23 | 2005-07-07 | Astrazeneca Ab | Diphenylazetidinone derivates possessing cholesterol absorption inhibitory activity |
US7901893B2 (en) * | 2004-01-16 | 2011-03-08 | Merck Sharp & Dohme Corp. | NPC1L1 (NPC3) and methods of identifying ligands thereof |
EP1807070A1 (en) * | 2004-09-29 | 2007-07-18 | Schering Corporation | Combinations of substituted azetidinones and cb1 antagonists |
CA2589483C (en) | 2004-12-03 | 2013-10-29 | Schering Corporation | Substituted piperazines as cb1 antagonists |
US8308559B2 (en) * | 2007-05-07 | 2012-11-13 | Jay Chun | Paradise box gaming system |
TW200726746A (en) | 2005-05-06 | 2007-07-16 | Microbia Inc | Processes for production of 4-biphenylylazetidin-2-ones |
CN101212978A (zh) * | 2005-05-09 | 2008-07-02 | 迈克罗比亚公司 | 有机金属苯基膦酸酯偶联剂 |
AU2006244043A1 (en) * | 2005-05-11 | 2006-11-16 | Microbia, Inc. | Processes for production of phenolic 4-biphenylylazetidin-2-ones |
BRPI0611415A2 (pt) * | 2005-05-25 | 2010-09-08 | Microbia Inc | ácidos fosfÈnicos de 4-(bifenilil)azetidin-2-ona e processo para a produção dos mesmos |
AU2006262441A1 (en) * | 2005-06-20 | 2007-01-04 | Schering Corporation | Piperidine derivatives useful as histamine H3 antagonists |
SA06270191B1 (ar) | 2005-06-22 | 2010-03-29 | استرازينيكا ايه بي | مشتقات من 2- أزيتيدينون جديدة باعتبارها مثبطات لامتصاص الكوليسترول لعلاج حالات فرط نسبة الدهون في الدم |
KR20070063592A (ko) * | 2005-09-08 | 2007-06-19 | 테바 파마슈티컬 인더스트리즈 리미티드 | 에제티밉의 합성을 위한 중간체인(3r,4s)-4-((4-벤질옥시)페닐)-1-(4-플루오로페닐)-3-((s)-3-(4-플루오로페닐)-3-히드록시프로필)-2-아제티디논의제조 방법 |
HUP0501164A2 (en) * | 2005-12-20 | 2007-07-30 | Richter Gedeon Nyrt | New industrial process for the production of ezetimibe |
CA2637565A1 (en) | 2006-01-18 | 2007-07-26 | Schering Corporation | Cannibinoid receptor modulators |
MX2008010235A (es) * | 2006-02-16 | 2008-10-23 | Kotobuki Pharmaceutical Co Ltd | Metodo para producir alcohol opticamente activo. |
US7910698B2 (en) | 2006-02-24 | 2011-03-22 | Schering Corporation | NPC1L1 orthologues |
AR060623A1 (es) | 2006-04-27 | 2008-07-02 | Astrazeneca Ab | Compuestos derivados de 2-azetidinona y un metodo de preparacion |
US20080103122A1 (en) * | 2006-09-05 | 2008-05-01 | Schering Corporation | Pharmaceutical combinations for lipid management and in the treatment of atherosclerosis and hepatic steatosis |
US20100197564A1 (en) * | 2007-04-19 | 2010-08-05 | Schering Corporation | Diaryl morpholines as cb1 modulators |
US20090047716A1 (en) * | 2007-06-07 | 2009-02-19 | Nurit Perlman | Reduction processes for the preparation of ezetimibe |
RU2010102478A (ru) * | 2007-06-28 | 2011-08-10 | Интэрвэт Интэрнэшнл Б.Ф. (NL) | Замещенные пиперазины как антагонисты св1 |
WO2009005671A2 (en) * | 2007-06-28 | 2009-01-08 | Schering Corporation | Substituted piperazines as cb1 antagonists |
WO2009032264A1 (en) * | 2007-08-30 | 2009-03-12 | Teva Pharmaceutical Industries Ltd. | Processes for preparing intermediates of ezetimibe by microbial reduction |
US20090312302A1 (en) * | 2008-06-17 | 2009-12-17 | Ironwood Pharmaceuticals, Inc. | Compositions and methods for treating nonalcoholic fatty liver disease-associated disorders |
CN102186972B (zh) | 2008-08-29 | 2014-08-20 | 科德克希思公司 | 用于立体选择性生产(4s)-3-[(5s)-5-(4-氟苯基)-5-羟基戊酰基]-4-苯基-1,3-噁唑烷-2-酮的酮还原酶多肽 |
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SG178456A1 (en) | 2009-08-19 | 2012-04-27 | Codexis Inc | Ketoreductase polypeptides for the preparation of phenylephrine |
EP2566497B1 (en) | 2010-05-04 | 2015-07-29 | Codexis, Inc. | Biocatalysts for ezetimibe synthesis |
WO2012155932A1 (en) | 2011-05-17 | 2012-11-22 | Pharmathen S.A. | Improved process for the preparation of ezetimibe |
CN111518046B (zh) * | 2020-06-04 | 2022-04-15 | 中山奕安泰医药科技有限公司 | 依泽替米贝中间体及依泽替米贝的制备方法 |
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-
2002
- 2002-03-25 RS YUP-748/03A patent/RS50386B/sr unknown
- 2002-03-25 AT AT02728561T patent/ATE305459T1/de active
- 2002-03-25 UA UA2003109666A patent/UA75644C2/uk unknown
- 2002-03-25 CZ CZ2003-2610A patent/CZ304929B6/cs not_active IP Right Cessation
- 2002-03-25 DE DE60206365T patent/DE60206365T2/de not_active Expired - Lifetime
- 2002-03-25 SK SK1186-2003A patent/SK287408B6/sk unknown
- 2002-03-25 EA EA200300970A patent/EA006898B1/ru not_active IP Right Cessation
- 2002-03-25 WO PCT/US2002/009123 patent/WO2002079174A2/en active IP Right Grant
- 2002-03-25 US US10/105,710 patent/US6627757B2/en not_active Expired - Lifetime
- 2002-03-25 PL PL363864A patent/PL205952B1/pl unknown
- 2002-03-25 MX MXPA03008803A patent/MXPA03008803A/es active IP Right Grant
- 2002-03-25 EP EP02728561A patent/EP1373230B1/en not_active Expired - Lifetime
- 2002-03-25 AU AU2002258605A patent/AU2002258605B2/en not_active Expired
- 2002-03-25 ES ES02728561T patent/ES2245733T3/es not_active Expired - Lifetime
- 2002-03-25 HU HU0303526A patent/HU230229B1/hu unknown
- 2002-03-25 EE EEP200300464A patent/EE05453B1/xx unknown
- 2002-03-25 IL IL15755202A patent/IL157552A0/xx unknown
- 2002-03-25 CN CNB028075374A patent/CN1275949C/zh not_active Expired - Lifetime
- 2002-03-25 SI SI200230193T patent/SI1373230T1/sl unknown
- 2002-03-25 CA CA002442219A patent/CA2442219C/en not_active Expired - Lifetime
- 2002-03-25 NZ NZ527852A patent/NZ527852A/en not_active IP Right Cessation
- 2002-03-25 KR KR1020037012486A patent/KR100590342B1/ko active IP Right Grant
- 2002-03-25 JP JP2002577801A patent/JP4145663B2/ja not_active Expired - Lifetime
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