AU2001230583A1 - Process for preparing optically active secondary alcohols having nitrogenous or oxygenic functional groups - Google Patents
Process for preparing optically active secondary alcohols having nitrogenous or oxygenic functional groupsInfo
- Publication number
- AU2001230583A1 AU2001230583A1 AU2001230583A AU3058301A AU2001230583A1 AU 2001230583 A1 AU2001230583 A1 AU 2001230583A1 AU 2001230583 A AU2001230583 A AU 2001230583A AU 3058301 A AU3058301 A AU 3058301A AU 2001230583 A1 AU2001230583 A1 AU 2001230583A1
- Authority
- AU
- Australia
- Prior art keywords
- nitrogenous
- functional groups
- optically active
- secondary alcohols
- active secondary
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
Links
- 125000000524 functional group Chemical group 0.000 title 1
- 238000004519 manufacturing process Methods 0.000 title 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 title 1
- 150000003333 secondary alcohols Chemical class 0.000 title 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/32—One oxygen, sulfur or nitrogen atom
- C07D239/42—One nitrogen atom
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C231/00—Preparation of carboxylic acid amides
- C07C231/16—Preparation of optical isomers
- C07C231/18—Preparation of optical isomers by stereospecific synthesis
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C233/00—Carboxylic acid amides
- C07C233/64—Carboxylic acid amides having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings
- C07C233/67—Carboxylic acid amides having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by singly-bound oxygen atoms
- C07C233/68—Carboxylic acid amides having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by singly-bound oxygen atoms with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by an acyclic carbon atom
- C07C233/73—Carboxylic acid amides having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by singly-bound oxygen atoms with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by an acyclic carbon atom of a carbon skeleton containing six-membered aromatic rings
-
- 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
- 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
- C07C303/36—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides of amides of sulfonic acids
- C07C303/40—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides of amides of sulfonic acids by reactions not involving the formation of sulfonamide groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C41/00—Preparation of ethers; Preparation of compounds having groups, groups or groups
- C07C41/01—Preparation of ethers
- C07C41/18—Preparation of ethers by reactions not forming ether-oxygen bonds
- C07C41/26—Preparation of ethers by reactions not forming ether-oxygen bonds by introduction of hydroxy or O-metal groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C41/00—Preparation of ethers; Preparation of compounds having groups, groups or groups
- C07C41/48—Preparation of compounds having groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/56—Ring systems containing three or more rings
- C07D209/80—[b, c]- or [b, d]-condensed
- C07D209/82—Carbazoles; Hydrogenated carbazoles
- C07D209/88—Carbazoles; Hydrogenated carbazoles 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 carbon atoms of the ring system
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/50—Organo-phosphines
- C07F9/5027—Polyphosphines
-
- 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)
- Life Sciences & Earth Sciences (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2000-30127 | 2000-02-08 | ||
| JP2000030127 | 2000-02-08 | ||
| PCT/JP2001/000797 WO2001058843A1 (en) | 2000-02-08 | 2001-02-05 | Process for preparing optically active secondary alcohols having nitrogenous or oxygenic functional groups |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AU2001230583A1 true AU2001230583A1 (en) | 2001-08-20 |
Family
ID=18555181
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU2001230583A Abandoned AU2001230583A1 (en) | 2000-02-08 | 2001-02-05 | Process for preparing optically active secondary alcohols having nitrogenous or oxygenic functional groups |
Country Status (4)
| Country | Link |
|---|---|
| US (1) | US20030045727A1 (en) |
| EP (1) | EP1254885A1 (en) |
| AU (1) | AU2001230583A1 (en) |
| WO (1) | WO2001058843A1 (en) |
Families Citing this family (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPWO2002074306A1 (en) * | 2001-03-19 | 2004-07-08 | 旭化成ファーマ株式会社 | Fatty liver treatment |
| JP4919562B2 (en) * | 2001-09-28 | 2012-04-18 | 日本曹達株式会社 | Ruthenium hydride complex, method for producing alcohol compound, and method for resolving racemic carbonyl compound |
| US6780810B2 (en) * | 2002-03-13 | 2004-08-24 | Council Of Scientific And Industrial Research | Multifunctional catalyst useful in the synthesis of chiral vicinal diols and process for the preparation thereof, and process for the preparation of chiral vicinal diols using said multifunctional catalysts |
| AU2002318538A1 (en) * | 2002-07-15 | 2004-02-02 | Nippon Soda Co., Ltd. | Ruthenium compounds, diamine ligands, and process for preparation of optically active alcohols |
| DE60318663T2 (en) | 2002-10-18 | 2008-06-05 | Yokozawa, Tohru, Fujisawa | Process for the preparation of optically active amino alcohols |
| AU2003277636A1 (en) * | 2002-11-15 | 2004-06-15 | Nippon Soda Co., Ltd. | Optically active, asymmetric binap derivative and optically active ruthenium compound |
| ES2336320T3 (en) * | 2002-12-05 | 2010-04-12 | Takeda Pharmaceutical Company Limited | TRANSITION METAL COMPLEX THAT HAS THE DIFFOSPHINE COMPLEX AS BINDING. |
| US6878838B2 (en) | 2003-03-24 | 2005-04-12 | The University Of North Carolina At Chapel Hill | Chiral porous metal phosphonates for heterogeneous asymmetric catalysis |
| JP2004346008A (en) * | 2003-05-22 | 2004-12-09 | Sumitomo Chem Co Ltd | Process for producing N-monoalkyl-3-hydroxy-3-arylpropylamines and intermediates |
| GB0316439D0 (en) * | 2003-07-15 | 2003-08-20 | Johnson Matthey Plc | Catalysts |
| US20070225528A1 (en) * | 2004-03-29 | 2007-09-27 | Nagoya Industrial Science Research Center | Process for Producing Optically Active Alcohol |
| PT1589019E (en) * | 2004-04-20 | 2008-10-08 | Ratiopharm Gmbh | Stereoselective process for the preparation of clopidogrel |
| WO2007082928A2 (en) * | 2006-01-23 | 2007-07-26 | Basf Se | Method for production of a ruthenium catalyst |
| CN101796050B (en) | 2007-09-06 | 2015-08-12 | 日本曹达株式会社 | The manufacture method of optical activity 3-quinuclidinol derivatives |
| KR101243408B1 (en) * | 2008-04-07 | 2013-03-13 | 닛뽕소다 가부시키가이샤 | Ruthenium compound and method for producing optically active aminoalcohol compound |
| JP5685071B2 (en) * | 2010-04-28 | 2015-03-18 | 高砂香料工業株式会社 | Novel ruthenium complex and method for producing optically active alcohol compound using the same as catalyst |
| CN102060877B (en) * | 2010-11-26 | 2014-07-23 | 中国科学院上海有机化学研究所 | Transition metal complex containing bidentate nitrogenous ligand, synthetic method and application thereof |
| EP2578570A1 (en) * | 2011-10-07 | 2013-04-10 | Almirall, S.A. | Novel process for preparing 5-(2-{[6-(2,2-difluoro-2-phenylethoxy)hexyl]amino}-1(r)-hydroxyethyl)-8-hydroxyquinolin-2(1h)-one via novel intermediates of synthesis. |
| JP5559767B2 (en) * | 2011-12-22 | 2014-07-23 | 日本曹達株式会社 | Ruthenium hydride complex |
| CN110590583A (en) * | 2019-09-23 | 2019-12-20 | 南方科技大学 | A kind of preparation method of denopamine and its intermediate |
| CN111320591B (en) * | 2020-03-30 | 2023-03-31 | 陕西师范大学 | Method for synthesizing chiral gamma-amino alcohol |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP4004123B2 (en) * | 1997-12-26 | 2007-11-07 | 独立行政法人科学技術振興機構 | Method for producing alcohol compound using ruthenium complex as catalyst |
-
2001
- 2001-02-05 AU AU2001230583A patent/AU2001230583A1/en not_active Abandoned
- 2001-02-05 EP EP01902770A patent/EP1254885A1/en not_active Withdrawn
- 2001-02-05 WO PCT/JP2001/000797 patent/WO2001058843A1/en not_active Ceased
- 2001-02-05 US US10/203,089 patent/US20030045727A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| WO2001058843A1 (en) | 2001-08-16 |
| EP1254885A1 (en) | 2002-11-06 |
| US20030045727A1 (en) | 2003-03-06 |
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