ECSP11011221A - Proceso para la preparación de compuestos ópticamente activos usando hidrogenación de transferencia - Google Patents
Proceso para la preparación de compuestos ópticamente activos usando hidrogenación de transferenciaInfo
- Publication number
- ECSP11011221A ECSP11011221A EC2011011221A ECSP11011221A ECSP11011221A EC SP11011221 A ECSP11011221 A EC SP11011221A EC 2011011221 A EC2011011221 A EC 2011011221A EC SP11011221 A ECSP11011221 A EC SP11011221A EC SP11011221 A ECSP11011221 A EC SP11011221A
- Authority
- EC
- Ecuador
- Prior art keywords
- preparation
- optically active
- active compounds
- transfer hydrogenation
- rivastigmine
- Prior art date
Links
- 238000000034 method Methods 0.000 title abstract 3
- 150000001875 compounds Chemical class 0.000 title abstract 2
- 238000009901 transfer hydrogenation reaction Methods 0.000 title abstract 2
- XSVMFMHYUFZWBK-NSHDSACASA-N Rivastigmine Chemical compound CCN(C)C(=O)OC1=CC=CC([C@H](C)N(C)C)=C1 XSVMFMHYUFZWBK-NSHDSACASA-N 0.000 abstract 2
- 229960004136 rivastigmine Drugs 0.000 abstract 2
- GQZXRLWUYONVCP-QMMMGPOBSA-N 3-[(1s)-1-(dimethylamino)ethyl]phenol Chemical compound CN(C)[C@@H](C)C1=CC=CC(O)=C1 GQZXRLWUYONVCP-QMMMGPOBSA-N 0.000 abstract 1
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 230000015572 biosynthetic process Effects 0.000 abstract 1
- 230000003197 catalytic effect Effects 0.000 abstract 1
- 238000010531 catalytic reduction reaction Methods 0.000 abstract 1
- 238000006243 chemical reaction Methods 0.000 abstract 1
- 229940079593 drug Drugs 0.000 abstract 1
- 239000003814 drug Substances 0.000 abstract 1
- 229940088679 drug related substance Drugs 0.000 abstract 1
- 239000000126 substance Substances 0.000 abstract 1
- 229940095064 tartrate Drugs 0.000 abstract 1
Classifications
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C37/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring
- C07C37/01—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring by replacing functional groups bound to a six-membered aromatic ring by hydroxy groups, e.g. by hydrolysis
- C07C37/055—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring by replacing functional groups bound to a six-membered aromatic ring by hydroxy groups, e.g. by hydrolysis the substituted group being bound to oxygen, e.g. ether group
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C269/00—Preparation of derivatives of carbamic acid, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
- C07C269/04—Preparation of derivatives of carbamic acid, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups from amines with formation of carbamate groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B53/00—Asymmetric syntheses
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C213/00—Preparation of compounds containing amino and hydroxy, amino and etherified hydroxy or amino and esterified hydroxy groups bound to the same carbon skeleton
- C07C213/02—Preparation of compounds containing amino and hydroxy, amino and etherified hydroxy or amino and esterified hydroxy groups bound to the same carbon skeleton by reactions involving the formation of amino groups from compounds containing hydroxy groups or etherified or esterified hydroxy groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C213/00—Preparation of compounds containing amino and hydroxy, amino and etherified hydroxy or amino and esterified hydroxy groups bound to the same carbon skeleton
- C07C213/08—Preparation of compounds containing amino and hydroxy, amino and etherified hydroxy or amino and esterified hydroxy groups bound to the same carbon skeleton by reactions not involving the formation of amino groups, hydroxy groups or etherified or esterified hydroxy groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C303/00—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides
- C07C303/26—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides of esters of sulfonic acids
- C07C303/28—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides of esters of sulfonic acids by reaction of hydroxy compounds with sulfonic acids or derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C303/00—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides
- C07C303/26—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides of esters of sulfonic acids
- C07C303/30—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides of esters of sulfonic acids by reactions not involving the formation of esterified sulfo groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C309/00—Sulfonic acids; Halides, esters, or anhydrides thereof
- C07C309/63—Esters of sulfonic acids
- C07C309/64—Esters of sulfonic acids having sulfur atoms of esterified sulfo groups bound to acyclic carbon atoms
- C07C309/65—Esters of sulfonic acids having sulfur atoms of esterified sulfo groups bound to acyclic carbon atoms of a saturated carbon skeleton
- C07C309/66—Methanesulfonates
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C37/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring
- C07C37/001—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring by modification in a side chain
- C07C37/002—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring by modification in a side chain by transformation of a functional group, e.g. oxo, carboxyl
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C39/00—Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a six-membered aromatic ring
- C07C39/02—Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a six-membered aromatic ring monocyclic with no unsaturation outside the aromatic ring
- C07C39/11—Alkylated hydroxy benzenes containing also acyclically bound hydroxy groups, e.g. saligenol
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
- C07B2200/07—Optical isomers
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- Neurosurgery (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Psychiatry (AREA)
- Animal Behavior & Ethology (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Hospice & Palliative Care (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Indole Compounds (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GBGB0823554.1A GB0823554D0 (en) | 2008-12-24 | 2008-12-24 | Process for the preparation of optically active compounds using transfer hydrogenation |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ECSP11011221A true ECSP11011221A (es) | 2011-08-31 |
Family
ID=40344210
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EC2011011221A ECSP11011221A (es) | 2008-12-24 | 2011-07-22 | Proceso para la preparación de compuestos ópticamente activos usando hidrogenación de transferencia |
Country Status (22)
| Country | Link |
|---|---|
| US (2) | US8415508B2 (enExample) |
| EP (1) | EP2382172A1 (enExample) |
| JP (1) | JP2012513966A (enExample) |
| KR (1) | KR20110098964A (enExample) |
| CN (1) | CN102264672A (enExample) |
| AR (1) | AR075496A1 (enExample) |
| AU (1) | AU2009331493B2 (enExample) |
| BR (1) | BRPI0923394A2 (enExample) |
| CA (1) | CA2748349A1 (enExample) |
| CL (1) | CL2011001563A1 (enExample) |
| CO (1) | CO6382153A2 (enExample) |
| EC (1) | ECSP11011221A (enExample) |
| GB (1) | GB0823554D0 (enExample) |
| IL (1) | IL213520A0 (enExample) |
| MA (1) | MA32983B1 (enExample) |
| MX (1) | MX2011006918A (enExample) |
| MY (1) | MY151103A (enExample) |
| NZ (1) | NZ593493A (enExample) |
| SG (1) | SG172052A1 (enExample) |
| TN (1) | TN2011000290A1 (enExample) |
| TW (1) | TW201035028A (enExample) |
| WO (1) | WO2010072798A1 (enExample) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103193600B (zh) * | 2012-01-07 | 2016-04-06 | 浙江九洲药物科技有限公司 | 卡巴拉汀中间体的制备方法 |
| EP3009419A4 (en) * | 2013-06-14 | 2017-01-18 | Nissan Chemical Industries, Ltd. | Production method for optically active alcohol compound |
| CN103980270A (zh) * | 2014-05-19 | 2014-08-13 | 埃斯特维华义制药有限公司 | 一种(r)-3-奎宁醇的制备方法 |
| CN108752322A (zh) * | 2018-09-12 | 2018-11-06 | 广州新民培林医药科技有限公司 | 一种新型Tepotinib衍生物和制备方法及其在抗肿瘤药物中的应用 |
| CN109809967B (zh) * | 2019-03-04 | 2022-03-18 | 陕西师范大学 | 一种合成手性醇的方法 |
Family Cites Families (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| HU201906B (en) * | 1987-03-04 | 1991-01-28 | Sandoz Ag | Process for producing phenyl-carbamate derivative and acid additional salts and pharmaceutical compositions containing them |
| US4996235A (en) * | 1987-11-25 | 1991-02-26 | Eli Lilly And Company | 3,4-diphenylbutanamines |
| JPH0899940A (ja) * | 1994-09-30 | 1996-04-16 | Kanegafuchi Chem Ind Co Ltd | 光学活性な1−(3,4−ジメトキシフェニル)−2−アミノプロパンの製造法 |
| GB9706321D0 (en) | 1997-03-26 | 1997-05-14 | Zeneca Ltd | Catalytic hydrogenation |
| JP3938651B2 (ja) * | 2000-04-13 | 2007-06-27 | セントラル硝子株式会社 | 光学活性α−メチル−ビス−3、5−(トリフルオロメチル)ベンジルアミンの製造方法 |
| KR20030062447A (ko) | 2000-12-25 | 2003-07-25 | 아지노모토 가부시키가이샤 | 광학 활성 할로하이드린 화합물의 제조방법 |
| DE602004017747D1 (de) * | 2003-07-08 | 2008-12-24 | Unilever Nv | Verfahren zur herstellung einer kosmetisch aktiven verbindung |
| GB0329284D0 (en) | 2003-12-18 | 2004-01-21 | Avecia Ltd | Process |
| US20070225528A1 (en) | 2004-03-29 | 2007-09-27 | Nagoya Industrial Science Research Center | Process for Producing Optically Active Alcohol |
| US6939981B1 (en) * | 2004-06-25 | 2005-09-06 | Eastman Chemical Company | Ruthenium complexes of phosphine-aminophosphine ligands |
| WO2006048720A1 (en) * | 2004-11-08 | 2006-05-11 | Emcure Pharmaceuticals Limited | An efficient method for preparation of (s)-3-[(1-dimethyl amino)ethyl]-phenyl-n-ethyl-n-methyl-carbamate |
| WO2006137167A1 (ja) * | 2005-06-20 | 2006-12-28 | Kanto Kagaku Kabushiki Kaisha | スルホナート触媒及びそれを利用したアルコール化合物の製法 |
| TWI389709B (zh) | 2005-12-01 | 2013-03-21 | Novartis Ag | 經皮治療系統 |
| WO2007147897A1 (de) | 2006-06-23 | 2007-12-27 | Basf Se | Verfahren zur herstellung von optisch aktiven 2-halogen-1-phenylethanol-derivaten und folgeprodukten davon |
| WO2009132443A1 (en) | 2008-05-01 | 2009-11-05 | Kanata Chemical Technologies Inc. | Cationic transition-metal arene catalysts |
-
2008
- 2008-12-24 GB GBGB0823554.1A patent/GB0823554D0/en not_active Ceased
-
2009
- 2009-12-17 US US12/653,748 patent/US8415508B2/en not_active Expired - Fee Related
- 2009-12-22 AR ARP090105061A patent/AR075496A1/es not_active Application Discontinuation
- 2009-12-23 WO PCT/EP2009/067821 patent/WO2010072798A1/en not_active Ceased
- 2009-12-23 MY MYPI20112891 patent/MY151103A/en unknown
- 2009-12-23 JP JP2011542822A patent/JP2012513966A/ja active Pending
- 2009-12-23 KR KR1020117017258A patent/KR20110098964A/ko not_active Ceased
- 2009-12-23 EP EP09799106A patent/EP2382172A1/en not_active Withdrawn
- 2009-12-23 SG SG2011042108A patent/SG172052A1/en unknown
- 2009-12-23 CA CA2748349A patent/CA2748349A1/en not_active Abandoned
- 2009-12-23 NZ NZ593493A patent/NZ593493A/xx not_active IP Right Cessation
- 2009-12-23 BR BRPI0923394A patent/BRPI0923394A2/pt not_active IP Right Cessation
- 2009-12-23 CN CN2009801523437A patent/CN102264672A/zh active Pending
- 2009-12-23 TW TW098144595A patent/TW201035028A/zh unknown
- 2009-12-23 MX MX2011006918A patent/MX2011006918A/es not_active Application Discontinuation
- 2009-12-23 MA MA34036A patent/MA32983B1/fr unknown
- 2009-12-23 AU AU2009331493A patent/AU2009331493B2/en not_active Ceased
-
2011
- 2011-06-09 TN TN2011000290A patent/TN2011000290A1/fr unknown
- 2011-06-13 IL IL213520A patent/IL213520A0/en unknown
- 2011-06-23 CL CL2011001563A patent/CL2011001563A1/es unknown
- 2011-06-29 CO CO11081447A patent/CO6382153A2/es active IP Right Grant
- 2011-07-22 EC EC2011011221A patent/ECSP11011221A/es unknown
-
2012
- 2012-12-05 US US13/705,884 patent/US8637713B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| CO6382153A2 (es) | 2012-02-15 |
| SG172052A1 (en) | 2011-07-28 |
| CL2011001563A1 (es) | 2012-01-13 |
| US8415508B2 (en) | 2013-04-09 |
| WO2010072798A1 (en) | 2010-07-01 |
| NZ593493A (en) | 2013-03-28 |
| JP2012513966A (ja) | 2012-06-21 |
| MY151103A (en) | 2014-04-15 |
| US8637713B2 (en) | 2014-01-28 |
| EP2382172A1 (en) | 2011-11-02 |
| US20100168229A1 (en) | 2010-07-01 |
| TN2011000290A1 (en) | 2012-12-17 |
| MA32983B1 (fr) | 2012-01-02 |
| AU2009331493B2 (en) | 2013-03-07 |
| KR20110098964A (ko) | 2011-09-02 |
| BRPI0923394A2 (pt) | 2016-01-12 |
| AU2009331493A1 (en) | 2011-07-07 |
| MX2011006918A (es) | 2011-07-29 |
| US20130096337A1 (en) | 2013-04-18 |
| IL213520A0 (en) | 2011-07-31 |
| CN102264672A (zh) | 2011-11-30 |
| GB0823554D0 (en) | 2009-01-28 |
| CA2748349A1 (en) | 2010-07-01 |
| AR075496A1 (es) | 2011-04-06 |
| TW201035028A (en) | 2010-10-01 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| MX336318B (es) | Co-cristales de tramadol y nsaids. | |
| CL2008000690A1 (es) | Compuestos derivados del acido indol-3-propionico; composicion farmaceutica; y uso en el tratamiento de enfermedades tales como hiperlipidemia, hipertension; entre otras. | |
| ECSP11011221A (es) | Proceso para la preparación de compuestos ópticamente activos usando hidrogenación de transferencia | |
| AR062148A1 (es) | Proceso quimico para la preparacion de intermediarios | |
| SMT201600216B (it) | Ottaidropirrolo[3,4.c]pirroli disostituiti come modulatori del recettore di orexina | |
| MX2022008867A (es) | Compuestos de benzaldehido sustituidos y metodos para su uso en incrementar la oxigenacion del tejido. | |
| BRPI0914549A2 (pt) | produção, formulação de usos de formulações estáveis de proteína harpina líquidas | |
| MX2010007846A (es) | Fabricación de enzimas sulfatasa lisosomal humana altamente fosforilada, activa y usos de las mismas. | |
| CL2008000434A1 (es) | Compuestos derivados de 2-amino-oxazolinas; proceso de obtencion; composicion farmaceutica; y uso en el tratamiento de enfermedades tales como depresion, ansiedad, estres, trastorno bipolar, entre otros. | |
| CL2011000668A1 (es) | Compuestos derivados de pirazolopiridina; proceso de preparacion; composicion farmaceutica y uso en el tratamiento de enfermedades tales como artritis reumatoide, psoriasis, esclerosis multiple, entre otras. | |
| BRPI1010550A2 (pt) | formas de dosagem, e, processo para a produção de preparações para formas de dosagem de substãncias ativas fracamente solúveis e, água. | |
| CO6311115A2 (es) | Membrana porosa no-biodegradable para soporte de crecimiento de células | |
| CR20110599A (es) | Composiciones farmacéuticamente activas que comprenden moduladores de estrés oxidativo (osm), nuevas entidades químicas, composiciones y usos | |
| CL2009000135A1 (es) | Compuestos derivados de 1,4-benzodiazepinas sustituidas, inhibidores de dipeptidilpeptidasa iv (dpp-iv); composicion farmaceutica; procedimiento de preparacion; y su uso en el tratamiento de enfermedades tales como diabetes tipo 2, cataratas, glaucoma, hipertrofia prostatica benigna, cancer, entre otras; compuestos intermediarios. | |
| CY1122416T1 (el) | Φαρμακα τα οποια περιεχουν κρυσταλλικες τροποποιησεις (1r,2r)-3-(3-δimeθyλamino-1-αιθυλο-2-μεθυλο-προπυλο)-φαινολης | |
| CL2009001684A1 (es) | Procedimiento de sintesis de agomelatina por reduccion de un grupo nitrilo en presencia de anhidrido acetico. | |
| CL2014000753A1 (es) | Proceso para la preparacion de n-((1r,2s,5r)-5-(tert-butilamino)-2-((s)-3-(7-tert-butilpirazolo(1,5-a)(1,3,5)triazin-4-ilamino)-2-oxopirrolidin-1-il)ciclohexil)acetamida, un modulador dual de la actividad del receptor de quimiocinas. (divisional sol. 924-2012) | |
| NI201400002A (es) | N - ( 6 - (( 2r, 3s) - 3, 4 - dihidroxibutan - 2 - iloxi) - 2 - ( 4 - fluorobenciltio ) pirimidin - 4 - il ) - 3 - metilacetidina - 1 - sulfonamida como modulador del receptor de quimiocina | |
| CL2014001309A1 (es) | Compuestos derivados de [1,2,3] triazolo [4,5-d]-pirimidina, agonistas del receptor de canabinoides 2; proceso de obtencion; composicion farmaceutica; uso para el tratamiento o la profilaxis del dolor, aterosclerosis,retinopatia diabetica, diabetes, fibrosis hepatica, fallo cardiaco, entre otras. | |
| RU2011134931A (ru) | Штамм enterococcus, используемый для приготовления кисломолочных напитков | |
| CL2014000328A1 (es) | Metodo para preparar composicion que contiene un portador de oxigeno termoestable; composicion farmacéutica que comprende hemoglobina. | |
| MX2016011476A (es) | Catalizadores de rutenio-fenol para reacciones de hidrogenacion por transferencia. | |
| WO2008005988A3 (en) | Production of stilbenes and derivatives in plant hairy root cultures | |
| IT1398304B1 (it) | Procedimento di produzione di supporto di dialcossimagnesio per catalizzatore per la polimerizzazione di olefine, procedimento di produzione di catalizzatore per la polimerizzazione di olefine impiegante il medesimo e procedimento di polimerizzazione di olefine impiegante il medesimo. | |
| CL2009001006A1 (es) | Compuestos derivados del acido 4-dimetil-aminobutirico; proceso de obtencion; composicion farmaceutica; y uso en el tratamiento o profilaxis de enfermedades tales como hiperglucemia, diabetes e hipertension entre otras. |