PE20060662A1 - Procedimiento para producir derivados de amina opticamente activos - Google Patents
Procedimiento para producir derivados de amina opticamente activosInfo
- Publication number
- PE20060662A1 PE20060662A1 PE2005001052A PE2005001052A PE20060662A1 PE 20060662 A1 PE20060662 A1 PE 20060662A1 PE 2005001052 A PE2005001052 A PE 2005001052A PE 2005001052 A PE2005001052 A PE 2005001052A PE 20060662 A1 PE20060662 A1 PE 20060662A1
- Authority
- PE
- Peru
- Prior art keywords
- procedure
- furan
- optically active
- tetrahidro
- indeno
- Prior art date
Links
- 238000000034 method Methods 0.000 title abstract 5
- 150000001412 amines Chemical class 0.000 title abstract 2
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 abstract 6
- 239000003054 catalyst Substances 0.000 abstract 3
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium on carbon Substances [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 abstract 1
- 239000003125 aqueous solvent Substances 0.000 abstract 1
- 230000015572 biosynthetic process Effects 0.000 abstract 1
- 239000007795 chemical reaction product Substances 0.000 abstract 1
- 239000013078 crystal Substances 0.000 abstract 1
- 239000000047 product Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/77—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems
-
- 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
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
- A61K31/34—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide
- A61K31/343—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide condensed with a carbocyclic ring, e.g. coumaran, bufuralol, befunolol, clobenfurol, amiodarone
-
- 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
- A61P15/18—Feminine contraceptives
-
- 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
-
- 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
-
- 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
- A61P25/06—Antimigraine agents
-
- 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
- A61P25/08—Antiepileptics; Anticonvulsants
-
- 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
- A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
- A61P25/16—Anti-Parkinson drugs
-
- 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
- A61P25/18—Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
-
- 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
- A61P25/20—Hypnotics; Sedatives
-
- 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
- A61P25/22—Anxiolytics
-
- 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
- A61P25/24—Antidepressants
-
- 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
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
- A61P27/06—Antiglaucoma agents or miotics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- 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
- A61P37/02—Immunomodulators
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P5/00—Drugs for disorders of the endocrine system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P5/00—Drugs for disorders of the endocrine system
- A61P5/24—Drugs for disorders of the endocrine system of the sex hormones
-
- 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
-
- 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
- A61P9/12—Antihypertensives
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/77—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D307/78—Benzo [b] furans; Hydrogenated benzo [b] furans
- C07D307/79—Benzo [b] furans; Hydrogenated benzo [b] furans with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to carbon atoms of the hetero ring
- C07D307/80—Radicals substituted by oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/77—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D307/78—Benzo [b] furans; Hydrogenated benzo [b] furans
- C07D307/79—Benzo [b] furans; Hydrogenated benzo [b] furans with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to carbon atoms of the hetero ring
- C07D307/81—Radicals substituted by nitrogen atoms not forming part of a nitro radical
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Biomedical Technology (AREA)
- Diabetes (AREA)
- Pain & Pain Management (AREA)
- Endocrinology (AREA)
- Psychiatry (AREA)
- Epidemiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Immunology (AREA)
- Ophthalmology & Optometry (AREA)
- Reproductive Health (AREA)
- Emergency Medicine (AREA)
- Gynecology & Obstetrics (AREA)
- Psychology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Anesthesiology (AREA)
- Hospice & Palliative Care (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Furan Compounds (AREA)
Abstract
REFERIDA A UN PROCEDIMIENTO PARA PRODUCIR (S)-2-(1,6,7,8-TETRAHIDRO-2H-INDENO[5,4b]FURAN-8-IL)ETILAMINA, CARACTERIZADO PORQUE COMPRENDE: (i) REDUCIR ASIMETRICAMENTE (E)-2-(1,6,7,8-TETRAHIDRO-2H-INDENO[5,4b]FURAN-8-IL)ETILAMINA CON UN CATALIZADOR Y (ii) REDUCIR CATALITICAMENTE EL PRODUCTO DE REACCION OBTENIDO EN (i) A UNA TEMPERATURA DE ENTRE 40°C Y 100°C Y A UN PH DE ENTRE 3 Y 9 CON UN CATALIZADOR. EL CATALIZADOR EN LA ETAPA (i) ES Ru-BINAP Y EN LA ETAPA (ii) ES Pd-C. TAMBIEN ESTA REFERIDA A UN PROCEDIMIENTO DE PREPARACION DE LOS CRISTALES DE (S)-N-[2-(1,6,7,8-TETRAHIDRO-2H-INDENO[5,4b]FURAN-8-IL)ETIL]PROPIONAMIDA, CARACTERIZADO POR: (a) LA PROPIONILACION DE (S)-2-(1,6,7,8-TETRAHIDRO-2H-INDENO[5,4b]FURAN-8-IL)ETILAMINA OBTENIDA EN EL PROCEDIMIENTO ANTERIOR Y (b) CRISTALIZAR AGREGANDO EL SOLVENTE ACUOSO A LA SOLUCION DE REACCION OBTENIDA EN LA ETAPA (a). DICHO PROCEDIMIENTO ES UTIL PARA PRODUCIR DERIVADOS DE AMINA OPTICAMENTE ACTIVOS CON ELEVADA PUREZA, EN DONDE SE SUPRIME LA FORMACION DE PRODUCTOS COLATERALES
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2004265307 | 2004-09-13 |
Publications (1)
Publication Number | Publication Date |
---|---|
PE20060662A1 true PE20060662A1 (es) | 2006-08-22 |
Family
ID=36059992
Family Applications (3)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PE2008001369A PE20081390A1 (es) | 2004-09-13 | 2005-09-09 | Procedimiento para producir derivados de amina opticamente activos |
PE2012001990A PE20130154A1 (es) | 2004-09-13 | 2005-09-09 | Procedimiento para producir derivados de amina opticamente activos |
PE2005001052A PE20060662A1 (es) | 2004-09-13 | 2005-09-09 | Procedimiento para producir derivados de amina opticamente activos |
Family Applications Before (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PE2008001369A PE20081390A1 (es) | 2004-09-13 | 2005-09-09 | Procedimiento para producir derivados de amina opticamente activos |
PE2012001990A PE20130154A1 (es) | 2004-09-13 | 2005-09-09 | Procedimiento para producir derivados de amina opticamente activos |
Country Status (32)
Country | Link |
---|---|
US (4) | US8097737B2 (es) |
EP (2) | EP2537842A1 (es) |
JP (2) | JP5127228B2 (es) |
KR (1) | KR101298335B1 (es) |
CN (2) | CN102516211A (es) |
AR (1) | AR050737A1 (es) |
AU (1) | AU2005283521B2 (es) |
BR (1) | BRPI0515170A (es) |
CA (2) | CA2764314C (es) |
CR (2) | CR8975A (es) |
EC (1) | ECSP077317A (es) |
ES (1) | ES2485890T3 (es) |
GE (1) | GEP20094725B (es) |
GT (2) | GT200500257A (es) |
HN (1) | HN2005000548A (es) |
IL (2) | IL181462A (es) |
MA (1) | MA28855B1 (es) |
MX (1) | MX2007002822A (es) |
MY (2) | MY147822A (es) |
NO (1) | NO20071866L (es) |
NZ (1) | NZ553562A (es) |
PA (1) | PA8645701A1 (es) |
PE (3) | PE20081390A1 (es) |
PH (1) | PH12012501172A1 (es) |
RU (1) | RU2385318C2 (es) |
SA (1) | SA05260347A (es) |
SG (1) | SG151330A1 (es) |
TW (1) | TWI400220B (es) |
UA (1) | UA95598C2 (es) |
UY (1) | UY29118A1 (es) |
WO (1) | WO2006030739A1 (es) |
ZA (1) | ZA200701724B (es) |
Families Citing this family (25)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2008123067A1 (ja) * | 2007-03-19 | 2008-10-16 | Takeda Pharmaceutical Company Limited | アリルアミン不斉水素化法 |
WO2008150953A1 (en) * | 2007-05-30 | 2008-12-11 | Dr. Reddy's Laboratories Ltd. | Process of making ramelteon and related substances |
WO2008151170A2 (en) * | 2007-05-31 | 2008-12-11 | Teva Pharmaceutical Industries Ltd. | Process for the synthesis of ramelteon and its intermediates |
WO2009060318A2 (en) * | 2007-07-12 | 2009-05-14 | Teva Pharmaceutical Industries Ltd. | Polymorphic forms of ramelteon and processes for preparation thereof |
CN101531647B (zh) * | 2008-03-13 | 2012-10-31 | 常州亚邦制药有限公司 | (±)-2-(1,6,7,8-四氢-2H-茚并[5,4-b]呋喃-8-基)乙胺的拆分方法 |
CN102099348A (zh) * | 2008-07-14 | 2011-06-15 | 力奇制药公司 | 作为用于制备拉米替隆的中间体的6,7-二氢-1h-吲哚并[5,4-b]呋喃-8(2h)-酮的合成方法 |
WO2010045565A1 (en) * | 2008-10-16 | 2010-04-22 | Teva Pharmaceutical Industries Ltd. | Process for the synthesis of ramelteon and its intermediates |
WO2010092107A1 (en) | 2009-02-12 | 2010-08-19 | Lek Pharmaceuticals D.D. | Synthesis of (s)-n-[2-(1,6,7,8-tetrahydro-2h-indeno-[5,4-b]furan-8-yl)ethyl]propionamide |
CN101824012B (zh) * | 2009-03-02 | 2011-12-07 | 四川大学 | 2-(1,6,7,8-四氢-2H-茚并-[5,4-b]呋喃-8-基)乙腈及其制备方法和用途 |
CA2754802A1 (en) | 2009-03-10 | 2010-09-16 | Industriale Chimica S.R.L. | Process for the preparation of ramelteon |
EP2243775A1 (en) | 2009-04-07 | 2010-10-27 | LEK Pharmaceuticals d.d. | Synthesis of 1-(2,3-Dihydrobenzofuran-4-YL)ethanone as intermediate in the preparation of ramelteon |
WO2011027323A1 (en) | 2009-09-03 | 2011-03-10 | Ranbaxy Laboratories Limited | Process for the preparation of ramelteon |
WO2011027319A1 (en) | 2009-09-03 | 2011-03-10 | Ranbaxy Laboratories Limited | Process for the preparation of an intermediate for ramelteon |
CN101648931B (zh) * | 2009-09-21 | 2012-05-09 | 四川大学 | 一种3-(2,3-二氢苯并呋喃-5-基)-丙酸的制备方法 |
CN101665477B (zh) * | 2009-09-21 | 2012-05-09 | 四川大学 | (e)-3-(苯并呋喃-5-基)丙烯酸酯类化合物、其制备方法和用途 |
CN102648192B (zh) | 2009-09-29 | 2015-08-26 | 广州南沙龙沙有限公司 | 1,2,6,7-四氢-8h-茚并[5,4-b] 呋喃-8-酮的制备方法 |
WO2012035303A2 (en) | 2010-09-17 | 2012-03-22 | Cipla Limited Et Al | A novel process for synthesis of ramelteon, and key intermediates for the synthesis of ramelteon |
CN103664849B (zh) * | 2012-08-31 | 2017-03-29 | 上海阳帆医药科技有限公司 | 制备2‑(1,6,7,8‑四氢‑2H‑茚并[5,4‑b]呋喃‑8‑亚基乙胺的方法 |
CN102924410A (zh) * | 2012-10-29 | 2013-02-13 | 华润赛科药业有限责任公司 | 一种雷美替胺的制备方法及其中间体 |
CN103396387A (zh) * | 2013-08-07 | 2013-11-20 | 安徽联创药物化学有限公司 | 雷美替胺中间体的制备方法 |
CN105277628B (zh) * | 2014-07-07 | 2017-05-31 | 南京长澳医药科技有限公司 | 通过高效液相色谱法分离测定雷美替胺及其杂质的方法 |
CN104402848B (zh) * | 2014-09-22 | 2017-02-08 | 珠海联邦制药股份有限公司 | 雷美替胺中的杂质化合物的制备方法及制备的标准品 |
CN105622557B (zh) * | 2014-11-05 | 2018-12-04 | 上海医药工业研究院 | 雷美替胺中间体及其制备方法 |
KR102359229B1 (ko) | 2020-04-16 | 2022-02-07 | 제이투에이치바이오텍 (주) | 라멜테온의 제조 방법 및 이러한 제조 방법에 이용되는 중간체 화합물 |
CN115477628A (zh) * | 2022-10-17 | 2022-12-16 | 江苏海悦康医药科技有限公司 | 一种雷美替胺二聚体的合成方法 |
Family Cites Families (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0757758B2 (ja) | 1988-10-24 | 1995-06-21 | 高砂香料工業株式会社 | ルテニウム―ホスフィン錯体 |
US6060503A (en) | 1991-12-02 | 2000-05-09 | Endorecherche, Inc. | Benzopyran-containing compounds and method for their use |
PT812835E (pt) | 1995-03-02 | 2001-08-30 | Sankyo Co | Derivados opticamente activos de tiazolidinona |
US6034239A (en) * | 1996-03-08 | 2000-03-07 | Takeda Chemical Industries, Ltd. | Tricyclic compounds, their production and use |
JP2884153B2 (ja) | 1996-03-08 | 1999-04-19 | 武田薬品工業株式会社 | 三環性化合物、その製造法および剤 |
CA2241666C (en) * | 1996-03-08 | 2007-11-06 | Takeda Chemical Industries, Ltd. | Tricyclic compounds, their production and use |
EP1199304A1 (en) * | 1997-03-05 | 2002-04-24 | Takeda Chemical Industries, Ltd. | Bicyclic compounds and pharmaceutical composition containing tricyclic compound for treating or preventing sleep disorders |
JP4242940B2 (ja) | 1997-02-13 | 2009-03-25 | 高砂香料工業株式会社 | 光学活性アミン誘導体の製造法 |
JP4081161B2 (ja) * | 1997-09-05 | 2008-04-23 | 武田薬品工業株式会社 | 光学活性化合物の製造法 |
JP3509637B2 (ja) * | 1998-06-09 | 2004-03-22 | 武田薬品工業株式会社 | 睡眠障害予防治療剤 |
ATE247967T1 (de) * | 1998-06-09 | 2003-09-15 | Takeda Chemical Industries Ltd | Pharmazeutische kombination mit einem trizyclischen komponent und mindestens einem aus zolpidem, zopiclone und brotizolam, zur behandlung von schlafstörungen |
JP3633895B2 (ja) | 2000-11-17 | 2005-03-30 | 武田薬品工業株式会社 | コポリビドン含有製剤 |
DE60142305D1 (de) * | 2000-11-17 | 2010-07-15 | Takeda Pharmaceutical | Pharmazeutische zubereitung enthaltend n-ä2-(1,6,7,8-tetrahydro-2h-indenoä5,4 büfuran-8-yl)ethylüpropionamid ummantelt mit einer copolyvidon-enthaltenden, polyäthylenglykolfreien umhüllung |
-
2005
- 2005-09-06 TW TW094130493A patent/TWI400220B/zh not_active IP Right Cessation
- 2005-09-09 PE PE2008001369A patent/PE20081390A1/es not_active Application Discontinuation
- 2005-09-09 PE PE2012001990A patent/PE20130154A1/es not_active Application Discontinuation
- 2005-09-09 PE PE2005001052A patent/PE20060662A1/es not_active Application Discontinuation
- 2005-09-12 NZ NZ553562A patent/NZ553562A/en not_active IP Right Cessation
- 2005-09-12 EP EP12182935A patent/EP2537842A1/en not_active Withdrawn
- 2005-09-12 SG SG200902222-9A patent/SG151330A1/en unknown
- 2005-09-12 KR KR1020077005754A patent/KR101298335B1/ko not_active Expired - Fee Related
- 2005-09-12 WO PCT/JP2005/016761 patent/WO2006030739A1/ja active Application Filing
- 2005-09-12 US US11/662,684 patent/US8097737B2/en active Active
- 2005-09-12 EP EP05782085.4A patent/EP1792899B1/en active Active
- 2005-09-12 RU RU2007113811/04A patent/RU2385318C2/ru not_active IP Right Cessation
- 2005-09-12 PH PH1/2012/501172A patent/PH12012501172A1/en unknown
- 2005-09-12 CA CA2764314A patent/CA2764314C/en active Active
- 2005-09-12 BR BRPI0515170-8A patent/BRPI0515170A/pt not_active IP Right Cessation
- 2005-09-12 MX MX2007002822A patent/MX2007002822A/es active IP Right Grant
- 2005-09-12 MY MYPI20054286A patent/MY147822A/en unknown
- 2005-09-12 CA CA2579121A patent/CA2579121C/en active Active
- 2005-09-12 AR ARP050103792A patent/AR050737A1/es not_active Application Discontinuation
- 2005-09-12 CN CN201110304598XA patent/CN102516211A/zh active Pending
- 2005-09-12 AU AU2005283521A patent/AU2005283521B2/en not_active Ceased
- 2005-09-12 JP JP2006535875A patent/JP5127228B2/ja active Active
- 2005-09-12 ES ES05782085.4T patent/ES2485890T3/es active Active
- 2005-09-12 GE GEAP20059926A patent/GEP20094725B/en unknown
- 2005-09-12 ZA ZA200701724A patent/ZA200701724B/xx unknown
- 2005-09-12 MY MYPI20091231A patent/MY158073A/en unknown
- 2005-09-12 UA UAA200702582A patent/UA95598C2/ru unknown
- 2005-09-12 CN CN2005800388478A patent/CN101056867B/zh active Active
- 2005-09-13 HN HN2005000548A patent/HN2005000548A/es unknown
- 2005-09-13 GT GT200500257A patent/GT200500257A/es unknown
- 2005-09-13 UY UY29118A patent/UY29118A1/es not_active Application Discontinuation
- 2005-09-13 GT GT200500257AK patent/GT200500257AA/es unknown
- 2005-09-13 PA PA20058645701A patent/PA8645701A1/es unknown
- 2005-11-08 SA SA05260347A patent/SA05260347A/ar unknown
-
2007
- 2007-02-20 IL IL181462A patent/IL181462A/en not_active IP Right Cessation
- 2007-03-06 CR CR8975A patent/CR8975A/es unknown
- 2007-03-09 MA MA29745A patent/MA28855B1/fr unknown
- 2007-03-13 EC EC2007007317A patent/ECSP077317A/es unknown
- 2007-04-12 NO NO20071866A patent/NO20071866L/no not_active Application Discontinuation
-
2010
- 2010-08-09 IL IL207510A patent/IL207510A/en not_active IP Right Cessation
-
2011
- 2011-12-14 US US13/325,946 patent/US20120088826A1/en not_active Abandoned
- 2011-12-21 CR CR20110698A patent/CR20110698A/es unknown
-
2012
- 2012-01-26 JP JP2012014435A patent/JP5615304B2/ja active Active
- 2012-08-29 US US13/597,361 patent/US8609871B2/en active Active
-
2013
- 2013-11-13 US US14/079,607 patent/US20140066499A1/en not_active Abandoned
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
PE20060662A1 (es) | Procedimiento para producir derivados de amina opticamente activos | |
AR068527A2 (es) | Un procedimiento para preparar monohidrato de bromuro de tiotropio cristalino | |
BRPI0418245B8 (pt) | composto derivado de nitróxi de prostaglandina, processo para preparar dito composto, composição farmacêutica compreendendo dito composto e usos destes | |
AR029857A1 (es) | Derivados de acidos sulfonil-amino-metil-benzoicos sustituidos y procedimiento para su preparacion | |
ES2173499T3 (es) | Sales de adicion de acidos de compuesto de piperidina opticamente activo y procedimiento para su preparacion. | |
UY26841A1 (es) | Sales estables de ácido o-acetilsalicílico con aminoácidos básicos | |
EA201070719A1 (ru) | Способ получения 2-[4-(3- или 2-фторбензилокси)бензиламино]пропанамидов с высокой степенью чистоты | |
CO5650226A2 (es) | Forma cristalina del agonista del receptor adrenergico beta | |
AR059763A2 (es) | Proceso para la preparacion de la forma polimorfa cristalina i de ritonavir | |
AR039857A1 (es) | Preparaciones de una sulfinilacetamida | |
AR050518A1 (es) | Proceso de amonolisis para la preparacion de intermedarios para inhibidores de dpp iv | |
PE20080365A1 (es) | Procedimiento para hacer sales de n-hidroxi-3-[4-[[[2-(2-metil-1h-indol-3-il)etil]amino]metil]fenil]-2e-2-propenamida | |
RU2008103699A (ru) | Кристаллические формы динатриевой соли n-(-5-хлорсалицило-)-8-аминокаприловой кислоты | |
AR043993A1 (es) | Procedimiento para la sintesis del acido (2s)-indolina-2-carboxilico y aplicacion en la sistesis del perindopril | |
PE20020845A1 (es) | Derivados de o -amino-n-hidroxi-acetamida | |
AR051341A1 (es) | Proceso para la preparacion de derivados de [1,4,5]-oxadiazepina | |
PT1272495E (pt) | Processo para a preparacao de cefoperazona de sodio altamente cristalina | |
PE20011260A1 (es) | Derivados de sulfonamida | |
AR060622A1 (es) | Proceso para la preparcion del ester 2-[ 4-(4- fluoro-2 - metil-1h -indol-5- iloxi)-5-metil pirrolo [2,1-f] [ 1,2,4] triazin -6-iloxi] -1- metiletilico del acido [(1r),2s ] -2- aminopropinoico | |
MXPA06000945A (es) | Preparacion de sales metalicas de acidos grasos de cadena mediana. | |
AR051933A1 (es) | Proceso para la preparacion de n-(3,5 dicloropirid-4-ilo)-4-difluormetoxi-8-metano sulfonamido-dibenzo[b,d] furano-1-carboxamida | |
ES2049700T1 (es) | Sal cristalina de la s-carboximetilcisteina lisina monohidratada y procedimiento para su fabricacion. | |
PE20091566A1 (es) | (R)-N*6*-ETIL-6,7-DIHIDRO-5H-INDENO[5,6-d]TIAZOL-2,6-DIAMINA Y SUS SALES Y UN PROCEDIMIENTO PARA SU PREPARACION | |
ES2195752B1 (es) | Procedimiento para la preparacion de polimorfos cristalinos de la sal sodica del fosinopril. | |
AR058168A1 (es) | Sintesis del alendronato de sodio trihidratado |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
FC | Refusal |