SG149879A1 - OPTICALLY ACTIVE QUATERNARY AMMONIUM SALT HAVING AXIAL ASYMMETRY AND PROCESS FOR PRODUCING α - AMINO ACID AND DERIVATIVE THEREOF WITH THE SAME - Google Patents

OPTICALLY ACTIVE QUATERNARY AMMONIUM SALT HAVING AXIAL ASYMMETRY AND PROCESS FOR PRODUCING α - AMINO ACID AND DERIVATIVE THEREOF WITH THE SAME

Info

Publication number
SG149879A1
SG149879A1 SG200900527-3A SG2009005273A SG149879A1 SG 149879 A1 SG149879 A1 SG 149879A1 SG 2009005273 A SG2009005273 A SG 2009005273A SG 149879 A1 SG149879 A1 SG 149879A1
Authority
SG
Singapore
Prior art keywords
derivative
producing
amino acid
quaternary ammonium
ammonium salt
Prior art date
Application number
SG200900527-3A
Other languages
English (en)
Inventor
Keiji Maruoka
Original Assignee
Nagase & 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 Nagase & Co Ltd filed Critical Nagase & Co Ltd
Publication of SG149879A1 publication Critical patent/SG149879A1/en

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D223/00—Heterocyclic compounds containing seven-membered rings having one nitrogen atom as the only ring hetero atom
    • C07D223/14—Heterocyclic compounds containing seven-membered rings having one nitrogen atom as the only ring hetero atom condensed with carbocyclic rings or ring systems
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/02—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
    • B01J31/0234—Nitrogen-, phosphorus-, arsenic- or antimony-containing compounds
    • B01J31/0235—Nitrogen containing compounds
    • B01J31/0237—Amines
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/02—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
    • B01J31/0234—Nitrogen-, phosphorus-, arsenic- or antimony-containing compounds
    • B01J31/0235—Nitrogen containing compounds
    • B01J31/0239—Quaternary ammonium compounds
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C229/00—Compounds containing amino and carboxyl groups bound to the same carbon skeleton
    • C07C229/02—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton
    • C07C229/34—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton containing six-membered aromatic rings
    • C07C229/36—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton containing six-membered aromatic rings with at least one amino group and one carboxyl group bound to the same carbon atom of the carbon skeleton
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/10—Spiro-condensed systems
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/10—Spiro-condensed systems
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2231/00—Catalytic reactions performed with catalysts classified in B01J31/00
    • B01J2231/40—Substitution reactions at carbon centres, e.g. C-C or C-X, i.e. carbon-hetero atom, cross-coupling, C-H activation or ring-opening reactions
    • B01J2231/42—Catalytic cross-coupling, i.e. connection of previously not connected C-atoms or C- and X-atoms without rearrangement
    • B01J2231/4205—C-C cross-coupling, e.g. metal catalyzed or Friedel-Crafts type
    • B01J2231/4272—C-C cross-coupling, e.g. metal catalyzed or Friedel-Crafts type via enolates or aza-analogues, added as such or made in-situ, e.g. ArY + R2C=C(OM)Z -> ArR2C-C(O)Z, in which R is H or alkyl, M is Na, K or SiMe3, Y is the leaving group, Z is Ar or OR' and R' is alkyl
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
    • B01J2531/90—Catalytic systems characterized by the solvent or solvent system used
    • B01J2531/98—Phase-transfer catalysis in a mixed solvent system containing at least 2 immiscible solvents or solvent phases

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Other In-Based Heterocyclic Compounds (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Polarising Elements (AREA)
SG200900527-3A 2004-01-30 2005-01-27 OPTICALLY ACTIVE QUATERNARY AMMONIUM SALT HAVING AXIAL ASYMMETRY AND PROCESS FOR PRODUCING α - AMINO ACID AND DERIVATIVE THEREOF WITH THE SAME SG149879A1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2004023317 2004-01-30
JP2004056659 2004-03-01

Publications (1)

Publication Number Publication Date
SG149879A1 true SG149879A1 (en) 2009-02-27

Family

ID=34829419

Family Applications (1)

Application Number Title Priority Date Filing Date
SG200900527-3A SG149879A1 (en) 2004-01-30 2005-01-27 OPTICALLY ACTIVE QUATERNARY AMMONIUM SALT HAVING AXIAL ASYMMETRY AND PROCESS FOR PRODUCING α - AMINO ACID AND DERIVATIVE THEREOF WITH THE SAME

Country Status (7)

Country Link
US (3) US7928224B2 (zh)
EP (1) EP1712549B1 (zh)
JP (2) JP4605606B2 (zh)
CN (1) CN1914177B (zh)
CA (1) CA2549431C (zh)
SG (1) SG149879A1 (zh)
WO (1) WO2005073196A1 (zh)

Families Citing this family (24)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1712549B1 (en) * 2004-01-30 2018-04-11 Nagase & Company, Ltd. Optically active quaternary ammonium salt having axial asymmetry and process for producing alpha-amino acid and derivative thereof with the same
JP4779109B2 (ja) * 2004-11-17 2011-09-28 国立大学法人京都大学 軸不斉を有する光学活性アミノ酸誘導体及び該アミノ酸誘導体を不斉触媒として用いる光学活性化合物の製造方法
JP5296375B2 (ja) 2005-03-03 2013-09-25 日本曹達株式会社 ２つの軸不斉を有する光学活性アンモニウム塩化合物の製造方法
JP5008553B2 (ja) * 2005-03-29 2012-08-22 長瀬産業株式会社 軸不斉を有する光学活性な４級アンモニウム塩およびそれを用いたα−アミノ酸およびその誘導体の製造方法
JP4879896B2 (ja) * 2005-07-29 2012-02-22 長瀬産業株式会社 アルジミンまたはその誘導体を用いる一置換アルキル化化合物の製造方法
JP4802191B2 (ja) * 2005-07-29 2011-10-26 長瀬産業株式会社 軸不斉を有する光学活性な４級アンモニウム塩およびそれを用いたα−アミノ酸およびその誘導体の製造方法
JP5344523B2 (ja) * 2005-12-26 2013-11-20 長瀬産業株式会社 立体選択的にストレッカー反応を進行させ得る触媒、およびそれを用いたα−アミノニトリル誘導体を立体選択的に製造するための方法
DE102006009518A1 (de) * 2006-03-01 2007-09-06 Studiengesellschaft Kohle Mbh Organische Salze sowie Verfahren zur Herstellung von chiralen organischen Verbindungen
JP5108777B2 (ja) 2006-09-28 2012-12-26 長瀬産業株式会社 軸不斉を有する光学活性な４級アンモニウム塩およびそれを用いたα−アミノ酸およびその誘導体の製造方法
JP5112670B2 (ja) * 2006-10-03 2013-01-09 日本曹達株式会社 置換アミノ酸シッフ塩基化合物の製造方法
US8507669B2 (en) 2008-04-11 2013-08-13 Nippon Soda Co., Ltd. Optically active dibenzazepine derivatives
CN102267946B (zh) * 2010-06-07 2014-09-10 中国科学院上海药物研究所 高光学纯度含手性联萘骨架的α-季碳氨基酸酯类化合物、其制备方法及用途
JP5673169B2 (ja) 2011-02-08 2015-02-18 住友化学株式会社 ４級アンモニウム塩及びそれを用いたシクロプロパン化合物の製造方法
ES2804528T3 (es) 2011-07-05 2021-02-08 Vertex Pharma Procesos y productos intermedios para la producción de azaindoles
JP2015003861A (ja) * 2011-10-18 2015-01-08 株式会社カネカ （ｒ）−２−アミノ−２−エチルヘキサノールの製造法
WO2013148550A1 (en) * 2012-03-30 2013-10-03 Merck Sharp & Dohme Corp. Asymmetric synthesis for preparing fluoroleucine alkyl esters
JP6119022B2 (ja) * 2012-06-05 2017-04-26 国立大学法人 岡山大学 軸不斉を有するピリジン誘導体又はその塩、及びその製造方法並びにそれからなる不斉触媒
JP5963140B2 (ja) * 2012-10-12 2016-08-03 国立大学法人金沢大学 不斉脱水縮合剤
JP2016074605A (ja) * 2013-02-18 2016-05-12 長瀬産業株式会社 アミノ酸の製造方法およびアミノ酸合成キット
CN103193673B (zh) * 2013-03-19 2014-07-23 淮海工学院 季铵盐支载(水杨醛缩氨基酸)的功能配体及其制备方法
JP2017014109A (ja) * 2013-11-21 2017-01-19 株式会社カネカ 光学活性２，６−ジメチルチロシン誘導体の製造法
CN108940361B (zh) * 2018-08-02 2020-12-01 吉林大学 一种手性离子型多孔有机聚合物材料及其制备方法与应用
CN112916042B (zh) * 2021-01-29 2021-10-22 兰州交通大学 基于四甲基螺二氢茚骨架的手性季铵盐相转移催化剂及制备方法
CN113354681A (zh) * 2021-05-07 2021-09-07 佛山奕安赛医药科技有限公司 L-络氨酸衍生物不对称催化合成方法

Family Cites Families (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6340753B1 (en) * 2000-04-21 2002-01-22 Nagase & Co., Ltd. Optically active quarternary ammonium salt with axial chirality, method for producing thereof, and application thereof for asymmetric synthesis of α-amino acid
JP4502293B2 (ja) * 1999-06-04 2010-07-14 長瀬産業株式会社 軸不斉を有する光学活性な４級アンモニウム塩、その製法およびα−アミノ酸誘導体の不斉合成への応用
US6441231B1 (en) * 2000-07-13 2002-08-27 Nagase & Co., Ltd. Optically active quarternary ammonium salt with axial chirality, method for producing thereof, and application thereof for asymmetric synthesis of α-amino acid
JP2002173492A (ja) 2000-12-07 2002-06-21 Nagase & Co Ltd 軸不斉を有する光学活性な４級アンモニウム塩とそれを用いたβ−ヒドロキシケトンの立体選択的合成
JP2002326992A (ja) * 2001-05-02 2002-11-15 Nagase & Co Ltd ビナフチル基およびビフェニル基を含むｎ−スピロ不斉相間移動触媒
JP4782329B2 (ja) 2001-07-02 2011-09-28 長瀬産業株式会社 キラル相間移動触媒およびそれを用いた不斉ペプチドの製造方法
JP4415543B2 (ja) 2002-12-13 2010-02-17 三菱化学株式会社 光学活性６，６’−ジメチル−１，１’−ビフェニル−２，２’−ジオール誘導体の製造方法
JP4360096B2 (ja) 2003-02-07 2009-11-11 東ソー株式会社 光学活性四級アンモニウム塩、その製造方法、及びこれを相間移動触媒として用いた光学活性α−アミノ酸誘導体の製造方法
JP4322051B2 (ja) 2003-06-03 2009-08-26 日本曹達株式会社 光学活性４級アンモニウム塩化合物およびその合成中間体
JP4474861B2 (ja) 2003-07-23 2010-06-09 東ソー株式会社 光学活性四級アンモニウム塩、その製造法、並びにそれを用いた光学活性α−アミノ酸誘導体の製造法
EP1650212B1 (en) * 2003-07-23 2012-11-14 Tosoh Corporation Optically active quaternary ammonium salt, process for producing the same, and process for producing optically active alpha-amino acid derivative with the same
EP1712549B1 (en) * 2004-01-30 2018-04-11 Nagase & Company, Ltd. Optically active quaternary ammonium salt having axial asymmetry and process for producing alpha-amino acid and derivative thereof with the same
WO2006054366A1 (ja) * 2004-11-22 2006-05-26 Nagase & Co., Ltd. 軸不斉を有する光学活性な４級アンモニウム塩を用いたアミノ酸およびその誘導体の製造方法
JP5296375B2 (ja) 2005-03-03 2013-09-25 日本曹達株式会社 ２つの軸不斉を有する光学活性アンモニウム塩化合物の製造方法
JP5008553B2 (ja) * 2005-03-29 2012-08-22 長瀬産業株式会社 軸不斉を有する光学活性な４級アンモニウム塩およびそれを用いたα−アミノ酸およびその誘導体の製造方法
JP4879896B2 (ja) * 2005-07-29 2012-02-22 長瀬産業株式会社 アルジミンまたはその誘導体を用いる一置換アルキル化化合物の製造方法
JP5108777B2 (ja) * 2006-09-28 2012-12-26 長瀬産業株式会社 軸不斉を有する光学活性な４級アンモニウム塩およびそれを用いたα−アミノ酸およびその誘導体の製造方法

Also Published As

Publication number Publication date
WO2005073196A1 (ja) 2005-08-11
CA2549431C (en) 2010-09-14
EP1712549B1 (en) 2018-04-11
CA2549431A1 (en) 2005-08-11
US20110152562A1 (en) 2011-06-23
US7928224B2 (en) 2011-04-19
EP1712549A4 (en) 2009-08-05
CN1914177A (zh) 2007-02-14
US8716524B2 (en) 2014-05-06
JP4605606B2 (ja) 2011-01-05
JP2010222358A (ja) 2010-10-07
JPWO2005073196A1 (ja) 2007-11-15
JP5244149B2 (ja) 2013-07-24
CN1914177B (zh) 2011-10-12
US20070135654A1 (en) 2007-06-14
EP1712549A1 (en) 2006-10-18
US20070161624A1 (en) 2007-07-12
US8697910B2 (en) 2014-04-15

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