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 groups

Info

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
Application number
AU2001230583A
Inventor
Dai Ishii
Seiji Nakano
Ryoji Noyori
Takeshi Ohkuma
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Asahi Kasei Corp
Original Assignee
Asahi Kasei Corp
Asahi Chemical Industry Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Asahi Kasei Corp, Asahi Chemical Industry Co Ltd filed Critical Asahi Kasei Corp
Publication of AU2001230583A1 publication Critical patent/AU2001230583A1/en
Abandoned legal-status Critical Current

Links

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 System
    • 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
AU2001230583A 2000-02-08 2001-02-05 Process for preparing optically active secondary alcohols having nitrogenous or oxygenic functional groups Abandoned AU2001230583A1 (en)

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)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2002074306A1 (en) * 2001-03-19 2002-09-26 Asahi Kasei Kabushiki Kaisha Remedies for fatty liver
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
WO2004007506A1 (en) * 2002-07-15 2004-01-22 Nippon Soda Co.,Ltd. Ruthenium compounds, diamine ligands, and process for preparation of optically active alcohols
ATE384038T1 (en) * 2002-10-18 2008-02-15 Tohru Yokozawa METHOD FOR PRODUCING 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
KR101022686B1 (en) * 2002-12-05 2011-03-22 다케다 야쿠힌 고교 가부시키가이샤 Transition metal complex having diphosphine complex as ligand
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 Method for producing n-monoalkyl-3-hydroxy-3-arylpropylamine and intermediate therefor
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
SI1589019T1 (en) * 2004-04-20 2008-12-31 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
US8436181B2 (en) 2007-09-06 2013-05-07 Nippon Soda Co., Ltd. Production process of optically active 3-quinuclidinol derivative
CN101983186B (en) * 2008-04-07 2013-12-11 日本曹达株式会社 Ruthenium compound and method for producing optically active aminoalcohol compound
CN102858788B (en) * 2010-04-28 2016-01-27 高砂香料工业株式会社 Ruthenium complex and the method preparing optical activity alkylol cpd
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 Preparation method of dienopamine and intermediate thereof
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)

* Cited by examiner, † Cited by third party
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

Also Published As

Publication number Publication date
WO2001058843A1 (en) 2001-08-16
US20030045727A1 (en) 2003-03-06
EP1254885A1 (en) 2002-11-06

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