MX2007005169A - Procedimiento para el desenriquecimiento de substratos enantiomericamente enriquecidos. - Google Patents
Procedimiento para el desenriquecimiento de substratos enantiomericamente enriquecidos.Info
- Publication number
- MX2007005169A MX2007005169A MX2007005169A MX2007005169A MX2007005169A MX 2007005169 A MX2007005169 A MX 2007005169A MX 2007005169 A MX2007005169 A MX 2007005169A MX 2007005169 A MX2007005169 A MX 2007005169A MX 2007005169 A MX2007005169 A MX 2007005169A
- Authority
- MX
- Mexico
- Prior art keywords
- optionally substituted
- enantiomerically enriched
- heteroatom
- optionally
- enantiomer
- Prior art date
Links
- 239000000758 substrate Substances 0.000 title abstract 4
- 239000000203 mixture Substances 0.000 abstract 5
- 125000001183 hydrocarbyl group Chemical group 0.000 abstract 3
- 150000001875 compounds Chemical class 0.000 abstract 2
- 125000005842 heteroatom Chemical group 0.000 abstract 2
- 125000000623 heterocyclic group Chemical group 0.000 abstract 2
- HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 abstract 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 1
- 229910052799 carbon Inorganic materials 0.000 abstract 1
- 239000003054 catalyst Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B55/00—Racemisation; Complete or partial inversion
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B31/00—Reduction in general
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
- C07C29/132—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group
- C07C29/136—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group of >C=O containing groups, e.g. —COOH
- C07C29/143—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group of >C=O containing groups, e.g. —COOH of ketones
- C07C29/145—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group of >C=O containing groups, e.g. —COOH of ketones with hydrogen or hydrogen-containing gases
-
- 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)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Catalysts (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Abstract
Se provee un procedimiento para el desenriquecimiento de composiciones enantiomericamente enriquecidas que comprende hacer reaccionar una composicion enantiomericamente enriquecida que comprende por lo menos un primer enantiomero o diastereomero de un substrato que comprende un enlace carbono-heteroatomo, en donde el carbono es un centro quiral y el heteroatomo es un heteroatomo del grupo VI, en la presencia de un sistema catalizador y opcionalmente un promotor de reaccion para dar una composicion de producto que comprende primeros y segundos enantiomeros o diastereomeros del substrato que tiene un enlace carbono-heteroatomo, la relacion de segundo a primer enantiomero o diastereomero en la composicion de producto es mayor que la relacion de segundo a primer enantiomero o diastereomero en la composicion enantiomericamente enriquecida. Substratos preferidos incluyen compuestos de Formula (I) (ver Formula (1)) en donde X representa O, S; R1, R2 cada uno representa independientemente un hidrocarbilo opcionalmente substituido, un hidrocarbilo perthalogenado, un grupo heterociclico opcionalmente substituido; o R1 y R2 se unen opcionalmente a fin de formar un anillo(s) opcionalmente substituido; con la condicion de que R1, R2 se seleccionan de tal manera que * es un centro quiral. En un procedimiento preferido se puede obtener un compuesto de Formula (2) (ver Formula (2)) en donde: X representa O, S; R1, R2 cada uno representa independientemente un hidrocarbilo opcionalmente substituido, un hidrocarbilo perthalogenado, un grupo heterociclico opcionalmente substituido; o R1 y R2 se unen opcionalmente a fin de formar un anillo(s) opcionalmente substituido; con la condicion de que R1, R2 son diferentes.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GBGB0424000.8A GB0424000D0 (en) | 2004-10-29 | 2004-10-29 | Process |
| PCT/GB2005/004179 WO2006046062A1 (en) | 2004-10-29 | 2005-10-27 | Process for the de-enrichment of enantiomerically enriched substrates |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| MX2007005169A true MX2007005169A (es) | 2007-07-04 |
Family
ID=33515740
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MX2007005169A MX2007005169A (es) | 2004-10-29 | 2005-10-27 | Procedimiento para el desenriquecimiento de substratos enantiomericamente enriquecidos. |
Country Status (11)
| Country | Link |
|---|---|
| EP (1) | EP1809586A1 (es) |
| JP (1) | JP2008517990A (es) |
| KR (1) | KR20070068428A (es) |
| CN (1) | CN101052604A (es) |
| BR (1) | BRPI0517243A (es) |
| CA (1) | CA2583821A1 (es) |
| GB (1) | GB0424000D0 (es) |
| IL (1) | IL182589A0 (es) |
| MX (1) | MX2007005169A (es) |
| WO (1) | WO2006046062A1 (es) |
| ZA (1) | ZA200702979B (es) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP5212109B2 (ja) * | 2006-11-10 | 2013-06-19 | 和光純薬工業株式会社 | 金属触媒担持炭素−エチレンジアミン複合体及びその製造方法 |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5476964A (en) * | 1994-11-21 | 1995-12-19 | Uop | Continuous racemization of benzylic alcohols, ethers, and esters by solid acid catalyst |
| DE69635874T2 (de) * | 1995-12-06 | 2006-12-14 | Japan Science And Technology Agency, Kawaguchi | Verfahren zur Herstellung von optisch aktiven Alkoholen |
| CA2165125A1 (en) * | 1995-12-13 | 1997-06-14 | David W. House | Continuous process for racemization of benzylic alcohols, ethers, and esters by solid acid catalyst |
| GB0029356D0 (en) * | 2000-12-01 | 2001-01-17 | Avecia Ltd | Transfer hydrogenation |
| DE10062729A1 (de) * | 2000-12-15 | 2002-06-20 | Basf Ag | Verfahren zur Racemisierung von optisch aktiven Aminen |
| DE10133783A1 (de) * | 2001-07-16 | 2003-02-06 | Degussa | Verfahren zur Racemisierung von Alkoholen |
-
2004
- 2004-10-29 GB GBGB0424000.8A patent/GB0424000D0/en not_active Ceased
-
2005
- 2005-10-27 JP JP2007538513A patent/JP2008517990A/ja active Pending
- 2005-10-27 EP EP05804713A patent/EP1809586A1/en not_active Withdrawn
- 2005-10-27 KR KR1020077009554A patent/KR20070068428A/ko not_active Withdrawn
- 2005-10-27 CN CNA2005800374723A patent/CN101052604A/zh active Pending
- 2005-10-27 CA CA002583821A patent/CA2583821A1/en not_active Abandoned
- 2005-10-27 WO PCT/GB2005/004179 patent/WO2006046062A1/en not_active Ceased
- 2005-10-27 BR BRPI0517243-8A patent/BRPI0517243A/pt not_active Application Discontinuation
- 2005-10-27 MX MX2007005169A patent/MX2007005169A/es unknown
-
2007
- 2007-04-11 ZA ZA200702979A patent/ZA200702979B/xx unknown
- 2007-04-16 IL IL182589A patent/IL182589A0/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| GB0424000D0 (en) | 2004-12-01 |
| BRPI0517243A (pt) | 2008-10-07 |
| CN101052604A (zh) | 2007-10-10 |
| EP1809586A1 (en) | 2007-07-25 |
| IL182589A0 (en) | 2007-07-24 |
| JP2008517990A (ja) | 2008-05-29 |
| ZA200702979B (en) | 2008-08-27 |
| WO2006046062A1 (en) | 2006-05-04 |
| KR20070068428A (ko) | 2007-06-29 |
| CA2583821A1 (en) | 2006-05-04 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Fernández et al. | Asymmetric synthesis of alkane-and arenesulfinates of diacetone-D-glucose (DAG): an improved and general route to both enantiomerically pure sulfoxides | |
| JP5579178B2 (ja) | 2(s),4(s),5(s),7(s)−2,7−ジアルキル−4−ヒドロキシ−5−アミノ−8−アリール−オクタノイルアミドへの合成経路 | |
| SG170729A1 (en) | Processes and intermediates for preparing steric compounds | |
| CA2635917C (en) | Method for producing fluorinated organic compounds | |
| HU228815B1 (en) | Asymmetric synthesis of pregabalin | |
| TN2009000077A1 (en) | Process for preparing biaryl substituted 4-amino-butyric acid or derivatives thereof and their use in the production of nep inhibitors | |
| Sugimura et al. | Axial chirality control by 2, 4-pentanediol or its analogue as a simple chiral linking bridge. Highly diastereodifferentiating homocoupling of a 1-lithio-2-naphthyl ether | |
| SK100596A3 (en) | Process for enantioselective epoxidising prochiral olefins, a catalyst therefor and intermediates for making the catalyst | |
| JP5372771B2 (ja) | プロセス | |
| Ooi et al. | Asymmetric Synthesis of α‐Acyl‐γ‐butyrolactones Possessing All‐Carbon Quaternary Stereocenters by Phase‐Transfer‐Catalyzed Alkylation | |
| Watanabe et al. | An efficient access to both enantiomers of pipecolic acid | |
| EP0928787B1 (en) | Process for the preparation of 3-amino-pyrrolidine derivatives | |
| TNSN08142A1 (en) | Synthesis of renin inhibitors involving a cycloaddition reaction | |
| JP2019023181A (ja) | トファシチニブの調製のための有用な中間体であるキラル3−アミノ−ピペリジンの調製のための改良された方法 | |
| JPH04275258A (ja) | 光学活性1−アリール−アルキルアミン類のラセミ化方法 | |
| MX2007005169A (es) | Procedimiento para el desenriquecimiento de substratos enantiomericamente enriquecidos. | |
| JP2009518335A (ja) | 3−カルボキシ−2−オキソ−1−ピロリジン誘導体及びそれらの使用 | |
| Andersson et al. | Synthesis of two (S)-indoline-based chiral auxiliaries and their use in diastereoselective alkylation reactions | |
| Chênevert et al. | Chemoenzymatic enantoselective synthesis of (-)-indolizidine 167 B | |
| Shiina et al. | Kinetic Resolution of Racemic Secondary Benzylic Alcohols by the Enantioselective Esterification Using Pyridine‐3‐carboxylic Anhydride (3‐PCA) with Chiral Acyl‐Transfer Catalysts | |
| MX2007005170A (es) | Composiciones catalizadoras y su uso en el desenriquecimiento de substratos enantiomericamente enriquecidos. | |
| Enders et al. | Diastereo-and enantioselective synthesis of α, β-disubstituted γ-nitro methyl sulfonatesDedicated to Professor Helmut Zahn on the occasion of his 85th birthday. | |
| MY143324A (en) | Process for preparing phosphorus compounds having phosphate-phosphonate bond | |
| Vicario et al. | Asymmetric synthesis of 1, 2-diaryl-2-amino ethanols | |
| GB0229688D0 (en) | Solid-phase preparation of [18F] Fluorohaloalkanes |