WO2004110976A3 - Process for the preparation of aromatic amines - Google Patents

Process for the preparation of aromatic amines Download PDF

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Publication number
WO2004110976A3
WO2004110976A3 PCT/GB2004/002478 GB2004002478W WO2004110976A3 WO 2004110976 A3 WO2004110976 A3 WO 2004110976A3 GB 2004002478 W GB2004002478 W GB 2004002478W WO 2004110976 A3 WO2004110976 A3 WO 2004110976A3
Authority
WO
WIPO (PCT)
Prior art keywords
formula
compound
preparation
aromatic amines
give
Prior art date
Application number
PCT/GB2004/002478
Other languages
French (fr)
Other versions
WO2004110976A2 (en
Inventor
Andrew John Blacker
Juliette Martin
Original Assignee
Avecia Ltd
Andrew John Blacker
Juliette Martin
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 Avecia Ltd, Andrew John Blacker, Juliette Martin filed Critical Avecia Ltd
Priority to EP04736423A priority Critical patent/EP1636165A2/en
Priority to JP2006516396A priority patent/JP2006527255A/en
Priority to CA002529152A priority patent/CA2529152A1/en
Priority to US10/560,305 priority patent/US20060252964A1/en
Publication of WO2004110976A2 publication Critical patent/WO2004110976A2/en
Publication of WO2004110976A3 publication Critical patent/WO2004110976A3/en

Links

Classifications

    • 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
    • C07C209/00—Preparation of compounds containing amino groups bound to a carbon skeleton
    • C07C209/04—Preparation of compounds containing amino groups bound to a carbon skeleton by substitution of functional groups by amino groups
    • C07C209/14—Preparation of compounds containing amino groups bound to a carbon skeleton by substitution of functional groups by amino groups by substitution of hydroxy groups or of etherified or esterified hydroxy groups
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C209/00—Preparation of compounds containing amino groups bound to a carbon skeleton
    • C07C209/04—Preparation of compounds containing amino groups bound to a carbon skeleton by substitution of functional groups by amino groups
    • C07C209/14—Preparation of compounds containing amino groups bound to a carbon skeleton by substitution of functional groups by amino groups by substitution of hydroxy groups or of etherified or esterified hydroxy groups
    • C07C209/16—Preparation of compounds containing amino groups bound to a carbon skeleton by substitution of functional groups by amino groups by substitution of hydroxy groups or of etherified or esterified hydroxy groups with formation of amino groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C209/00—Preparation of compounds containing amino groups bound to a carbon skeleton
    • C07C209/82—Purification; Separation; Stabilisation; Use of additives
    • C07C209/86—Separation
    • C07C209/88—Separation of optical isomers
    • 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
    • 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
    • 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)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

Abstract

There is provided a process for the preparation of aromatic amines of Formula (1): where Rx is optionally substituted aryl and Ry is optionally substituted hydrocarbyl, which comprises: (a) reducing a compound of Formula (2): to give a compound of Formula (3): then, (b) reacting a compound of Formula (3) with a leaving group donor, to give a compound of Formula (4); and, (c) reacting a compound of Formula (4) with ammonia to give the compound of Formula (1).
PCT/GB2004/002478 2003-06-13 2004-06-09 Process for the preparation of aromatic amines WO2004110976A2 (en)

Priority Applications (4)

Application Number Priority Date Filing Date Title
EP04736423A EP1636165A2 (en) 2003-06-13 2004-06-09 Process for the preparation of aromatic amines
JP2006516396A JP2006527255A (en) 2003-06-13 2004-06-09 Process for the preparation of aromatic amines
CA002529152A CA2529152A1 (en) 2003-06-13 2004-06-09 Process for the preparation of aromatic amines
US10/560,305 US20060252964A1 (en) 2003-06-13 2004-06-09 Process for the preparation of aromatic amines

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GB0313661.1 2003-06-13
GBGB0313661.1A GB0313661D0 (en) 2003-06-13 2003-06-13 Process

Publications (2)

Publication Number Publication Date
WO2004110976A2 WO2004110976A2 (en) 2004-12-23
WO2004110976A3 true WO2004110976A3 (en) 2005-04-21

Family

ID=27590008

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/GB2004/002478 WO2004110976A2 (en) 2003-06-13 2004-06-09 Process for the preparation of aromatic amines

Country Status (7)

Country Link
US (1) US20060252964A1 (en)
EP (1) EP1636165A2 (en)
JP (1) JP2006527255A (en)
CN (1) CN1835909A (en)
CA (1) CA2529152A1 (en)
GB (1) GB0313661D0 (en)
WO (1) WO2004110976A2 (en)

Families Citing this family (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB0428128D0 (en) * 2004-12-22 2005-01-26 Avecia Ltd Process
BRPI0609580A2 (en) * 2005-03-22 2010-04-20 Hoffmann La Roche compound, crystalline polymorph, process for its manufacture, pharmaceutical compositions containing it, method for the treatment and / or prophylaxis of diseases that are associated with dpp-iv and use of the compound
WO2008058235A2 (en) * 2006-11-08 2008-05-15 Dr. Reddy's Laboratories, Ltd. Processes for the preparation of cinacalcet
CN101407465B (en) * 2007-10-12 2013-06-05 天津药明康德新药开发有限公司 Method for preparing optical pure 1-(1-naphthyl)ethylamine by separation
JP5727127B2 (en) 2009-04-10 2015-06-03 関東化学株式会社 Asymmetric catalyst and method for producing optically active alcohols using the same
CN102617500B (en) * 2011-01-31 2016-07-13 山东信立泰药业有限公司 A kind of preparation method of linezolid intermediate, its preparation method and Linezolid
WO2014178068A2 (en) * 2013-04-08 2014-11-06 Cadila Healthcare Limited An improved process for preparation of n-[1-(1-naphthyl)ethyl] -3- [3-(trifluoromethyl)phenyl]propan-1-amine and pharmaceutically acceptable salts thereof
CN103420845B (en) * 2013-08-21 2015-09-02 中国药科大学 One prepares the method for cinacalcet intermediate R-(+)-1-(1-naphthyl) ethamine
CN105294449B (en) * 2014-06-16 2017-02-08 连云港手性化学有限公司 Preparation method for (R)-(+)-1-(1-naphthyl)ethylamine and (S)-(-)-1-(1-naphthyl)ethylamine
CN104151171B (en) * 2014-08-14 2016-07-27 六安佳诺生化科技有限公司 The method of optical voidness R-1-naphthalene ethylamine is prepared in a kind of fractionation
WO2017033134A1 (en) 2015-08-26 2017-03-02 Lupin Limited Enzymatic process for the for preparation of (r)-1-(1-naphthyl) ethylamine, an intermediate of cinacalcet hydrochloride
CN105085244A (en) * 2015-08-31 2015-11-25 彭静 Preparing method of (R)-(+)-4-bromomandelic acid
CN105085245A (en) * 2015-08-31 2015-11-25 彭静 Preparing method of (R)-(+)-4-fluoromandelic acid
CN105085235A (en) * 2015-08-31 2015-11-25 彭静 Method for splitting and preparing S-4-chloro mandelic acid
CN105085234A (en) * 2015-08-31 2015-11-25 彭静 Preparing method of (R)-(-)-4-chloromandelic acid
CN105085236A (en) * 2015-09-02 2015-11-25 彭静 Resolution preparation method of R-pentafluoro DL-mandelic acid
CN105061190A (en) * 2015-09-02 2015-11-18 彭静 Method for preparing S-five-fluorine amygdalic acid through resolution
CN105085247A (en) * 2015-09-02 2015-11-25 彭静 Resolution preparation method of R-4-methoxymandelic acid
TWI784593B (en) 2021-06-22 2022-11-21 陳慶祥 tattoo machine

Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1986001502A1 (en) * 1984-08-28 1986-03-13 Diamalt Aktiengesellschaft Process for the production of amino compounds from hydroxyl compounds
US5767276A (en) * 1995-10-13 1998-06-16 The Penn State Research Foundation Asymmetric synthesis catalyzed by transition metal complexes with new chiral ligands
WO1998042643A1 (en) * 1997-03-26 1998-10-01 Avecia Limited Transfer hydrogenation process and catalyst
WO1999024410A1 (en) * 1997-11-12 1999-05-20 The Penn State Research Foundation Transition metal-catalyzed reactions based on chiral amine oxazolinyl ligands
WO2000066558A1 (en) * 1999-05-04 2000-11-09 Schering Corporation Piperazine derivatives useful as ccr5 antagonists
JP2001294568A (en) * 2000-04-13 2001-10-23 Central Glass Co Ltd METHOD FOR PRODUCING OPTICALLY ACTIVE alpha-METHYL-BIS-3,5-(TRI- FLUOROMETHYL)BENZYLAMINE
US6391865B1 (en) * 1999-05-04 2002-05-21 Schering Corporation Piperazine derivatives useful as CCR5 antagonists

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1986001502A1 (en) * 1984-08-28 1986-03-13 Diamalt Aktiengesellschaft Process for the production of amino compounds from hydroxyl compounds
US5767276A (en) * 1995-10-13 1998-06-16 The Penn State Research Foundation Asymmetric synthesis catalyzed by transition metal complexes with new chiral ligands
WO1998042643A1 (en) * 1997-03-26 1998-10-01 Avecia Limited Transfer hydrogenation process and catalyst
WO1999024410A1 (en) * 1997-11-12 1999-05-20 The Penn State Research Foundation Transition metal-catalyzed reactions based on chiral amine oxazolinyl ligands
WO2000066558A1 (en) * 1999-05-04 2000-11-09 Schering Corporation Piperazine derivatives useful as ccr5 antagonists
US6391865B1 (en) * 1999-05-04 2002-05-21 Schering Corporation Piperazine derivatives useful as CCR5 antagonists
JP2001294568A (en) * 2000-04-13 2001-10-23 Central Glass Co Ltd METHOD FOR PRODUCING OPTICALLY ACTIVE alpha-METHYL-BIS-3,5-(TRI- FLUOROMETHYL)BENZYLAMINE

Non-Patent Citations (8)

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DATABASE CROSSFIRE BEILSTEIN BEILSTEIN INSTITUT ZUR FOERDERUNG DER CHEMISCHEN WISSENSCHAFTEN, FRANFURKT AM MAIN, DE; XP002300107 *
JAYARAM R. TAGAT ET AL.: "Piperazine-based CCR5 antagonists as HIV-1 inhibitors.", JOURNAL OF MEDICINAL CHEMISTRY., vol. 44, no. 21, 2001, USAMERICAN CHEMICAL SOCIETY. WASHINGTON., pages 3343 - 3346, XP002300104 *
JOURNAL OF ORGANIC CHEMISTRY., vol. 60, no. 26, 1995, USAMERICAN CHEMICAL SOCIETY, WASHINGTON, DC., pages 8424 - 8427 *
PATENT ABSTRACTS OF JAPAN vol. 2002, no. 02 2 April 2002 (2002-04-02) *
RANU B C ET AL: "Reduction of trihalomethyl carbinols and their acetates, mesylates and tosylates by indium metal", TETRAHEDRON LETTERS, ELSEVIER SCIENCE PUBLISHERS, AMSTERDAM, NL, vol. 43, no. 34, 19 August 2002 (2002-08-19), pages 5993 - 5995, XP004373219, ISSN: 0040-4039 *
THOMAS M. STEIN ET AL.: "Synthesis and aggregation properties of a new family of amphiphiles with an unusual headgroup topology", JOURNAL OF THE AMERICAN CHEMICAL SOCIETY., vol. 114, no. 10, 1992, USAMERICAN CHEMICAL SOCIETY, WASHINGTON, DC., pages 3943 - 3950, XP002300106 *
W. H. PIRKLE ET AL.: "High pressure assisted synthesis.", JOURNAL OF ORGANIC CHEMISTRY., vol. 42, no. 18, 1977, USAMERICAN CHEMICAL SOCIETY, WASHINGTON, DC., pages 3101 - 3103, XP002300103 *

Also Published As

Publication number Publication date
CA2529152A1 (en) 2004-12-23
CN1835909A (en) 2006-09-20
US20060252964A1 (en) 2006-11-09
GB0313661D0 (en) 2003-07-16
WO2004110976A2 (en) 2004-12-23
JP2006527255A (en) 2006-11-30
EP1636165A2 (en) 2006-03-22

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