WO2012150280A3 - Preparation of 4,4-dialkoxy-1-buten-1-ylarenes - Google Patents

Preparation of 4,4-dialkoxy-1-buten-1-ylarenes Download PDF

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Publication number
WO2012150280A3
WO2012150280A3 PCT/EP2012/058070 EP2012058070W WO2012150280A3 WO 2012150280 A3 WO2012150280 A3 WO 2012150280A3 EP 2012058070 W EP2012058070 W EP 2012058070W WO 2012150280 A3 WO2012150280 A3 WO 2012150280A3
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WO
WIPO (PCT)
Prior art keywords
buten
preparation
ylarenes
dialkoxy
als
Prior art date
Application number
PCT/EP2012/058070
Other languages
French (fr)
Other versions
WO2012150280A2 (en
Inventor
Florencio Zaragoza Doerwald
Verena HEINZE
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Lonza 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 Lonza Ltd filed Critical Lonza Ltd
Publication of WO2012150280A2 publication Critical patent/WO2012150280A2/en
Publication of WO2012150280A3 publication Critical patent/WO2012150280A3/en

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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C205/00Compounds containing nitro groups bound to a carbon skeleton
    • C07C205/27Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by etherified hydroxy groups
    • C07C205/34Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by etherified hydroxy groups having nitro groups bound to carbon atoms of six-membered aromatic rings and etherified hydroxy groups bound to acyclic carbon atoms of the carbon skeleton
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C201/00Preparation of esters of nitric or nitrous acid or of compounds containing nitro or nitroso groups bound to a carbon skeleton
    • C07C201/06Preparation of nitro compounds
    • C07C201/12Preparation of nitro compounds by reactions not involving the formation of nitro groups
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C245/00Compounds containing chains of at least two nitrogen atoms with at least one nitrogen-to-nitrogen multiple bond
    • C07C245/20Diazonium compounds
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C41/00Preparation of ethers; Preparation of compounds having groups, groups or groups
    • C07C41/48Preparation of compounds having groups
    • C07C41/50Preparation of compounds having groups by reactions producing groups
    • C07C41/56Preparation of compounds having groups by reactions producing groups by condensation of aldehydes, paraformaldehyde, or ketones
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C43/00Ethers; Compounds having groups, groups or groups
    • C07C43/30Compounds having groups
    • C07C43/303Compounds having groups having acetal carbon atoms bound to acyclic carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C43/00Ethers; Compounds having groups, groups or groups
    • C07C43/30Compounds having groups
    • C07C43/313Compounds having groups containing halogen
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/51Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by pyrolysis, rearrangement or decomposition
    • C07C45/511Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by pyrolysis, rearrangement or decomposition involving transformation of singly bound oxygen functional groups to >C = O groups
    • C07C45/515Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by pyrolysis, rearrangement or decomposition involving transformation of singly bound oxygen functional groups to >C = O groups the singly bound functional group being an acetalised, ketalised hemi-acetalised, or hemi-ketalised hydroxyl group
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C47/00Compounds having —CHO groups
    • C07C47/20Unsaturated compounds having —CHO groups bound to acyclic carbon atoms
    • C07C47/24Unsaturated compounds having —CHO groups bound to acyclic carbon atoms containing halogen
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C67/00Preparation of carboxylic acid esters
    • C07C67/30Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group
    • C07C67/333Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group by isomerisation; by change of size of the carbon skeleton
    • C07C67/343Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C69/00Esters of carboxylic acids; Esters of carbonic or haloformic acids
    • C07C69/76Esters of carboxylic acids having a carboxyl group bound to a carbon atom of a six-membered aromatic ring

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

The invention discloses a method for the preparation of 4,4-dialkoxy-1-buten-1-ylarenes from crotonaldehyde and aryldiazonium salts, n-buten-1-als and n-butan-1-als derived thereof, their use as fragrances, use of this method in and intermediates for the preparation of antineoplastic antifolates or folate anitmetabolitesor Pemetrexed.
PCT/EP2012/058070 2011-05-05 2012-05-03 Preparation of 4,4-dialkoxy-1-buten-1-ylarenes WO2012150280A2 (en)

Applications Claiming Priority (6)

Application Number Priority Date Filing Date Title
US201161482839P 2011-05-05 2011-05-05
EP11003685 2011-05-05
US61/482,839 2011-05-05
EP11003685.2 2011-05-05
EP11186633 2011-10-26
EP11186633.1 2011-10-26

Publications (2)

Publication Number Publication Date
WO2012150280A2 WO2012150280A2 (en) 2012-11-08
WO2012150280A3 true WO2012150280A3 (en) 2013-01-10

Family

ID=47108085

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/EP2012/058070 WO2012150280A2 (en) 2011-05-05 2012-05-03 Preparation of 4,4-dialkoxy-1-buten-1-ylarenes

Country Status (2)

Country Link
TW (1) TW201307276A (en)
WO (1) WO2012150280A2 (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105111214B (en) * 2015-08-31 2017-10-31 江西农业大学 A kind of preparation method of pemetrexed disodium
CN105601493A (en) * 2015-12-23 2016-05-25 江苏师范大学 Preparation method and application of alkannin analogue based on anthraquinone structure

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NL7502553A (en) * 1975-02-13 1976-08-17 Ruhrchemie Ag Hydroformylated tert. butyl- and isopropyl allyl benzenes - useful aromatizing cpds
WO1999016742A1 (en) * 1997-09-26 1999-04-08 Eli Lilly And Company Processes and intermediates useful to make antifolates
CN101085775A (en) * 2007-07-06 2007-12-12 吴洪流 Pemetrexed intermediate and preparation method thereof

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NL7502553A (en) * 1975-02-13 1976-08-17 Ruhrchemie Ag Hydroformylated tert. butyl- and isopropyl allyl benzenes - useful aromatizing cpds
WO1999016742A1 (en) * 1997-09-26 1999-04-08 Eli Lilly And Company Processes and intermediates useful to make antifolates
CN101085775A (en) * 2007-07-06 2007-12-12 吴洪流 Pemetrexed intermediate and preparation method thereof

Non-Patent Citations (28)

* Cited by examiner, † Cited by third party
Title
ALHAFFAR, M. ET AL.: "Ultranox626 as a selective ligand in rhodium-catalyzed hydroformylation-acetalization of alkylbenzene derivatives", REAC. KINET. MECH. CAT., vol. 104, 12 July 2011 (2011-07-12), pages 323 - 336, XP002685180 *
ASLANIAN R ET AL: "Structural determinants for histamine H1 affinity, hERG affinity and QTc prolongation in a series of terfenadine analogs", BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, vol. 19, no. 17, 1 September 2009 (2009-09-01), PERGAMON, ELSEVIER SCIENCE, GB, pages 5043 - 5047, XP026458554, ISSN: 0960-894X, [retrieved on 20090805] *
BANERJEE, AJOY K. ET AL: "Acid catalyzed novel rearrangement of bicyclic dienone", TETRAHEDRON, vol. 41, no. 15, 1985, pages 3029 - 3032, XP055047987, ISSN: 0040-4020, DOI: doi:10.1016/S0040-4020(01)96654-2 *
BROGAN, ANDREW P. ET AL: "Nornicotine-organocatalyzed aqueous reduction of .alpha.,.beta.-unsaturated aldehydes", CHEMICAL COMMUNICATIONS (CAMBRIDGE, UNITED KINGDOM) , (46), 4952-4954 CODEN: CHCOFS; ISSN: 1359-7345, 2007 *
BULLETIN DE LA SOCIETE CHIMIQUE DE FRANCE, 1961, pages 2396 - 2401, ISSN: 0037-8968 *
CHEN, JIAN ET AL: "A practical and mild method for the highly selective conversion of terminal alkenes into aldehydes through epoxidation-isomerization with ruthenium(IV)-porphyrin catalysts", ANGEWANDTE CHEMIE, INTERNATIONAL EDITION , 43(37), 4950-4954, S4950/1-S4950/6 CODEN: ACIEF5; ISSN: 1433-7851, 2004 *
CHOUDARY, B. M. ET AL: "The first example of activation of molecular oxygen by nickel in Ni-Al hydrotalcite: a novel protocol for the selective oxidation of alcohols", ANGEWANDTE CHEMIE, INTERNATIONAL EDITION, vol. 40, no. 4, 2001, pages 763 - 766, XP001004951, ISSN: 1433-7851, DOI: doi:10.1002/1521-3773(20010216)40:4<763::AID-ANIE7630>3.3.CO;2-K *
DATABASE CA [online] CHEMICAL ABSTRACTS SERVICE, COLUMBUS, OHIO, US; BANERJEE, AJOY K. ET AL: "Acid catalyzed novel rearrangement of bicyclic dienone", XP002685184, retrieved from STN Database accession no. 1986:206824 *
DATABASE CA [online] CHEMICAL ABSTRACTS SERVICE, COLUMBUS, OHIO, US; BROGAN, ANDREW P. ET AL: "Nornicotine-organocatalyzed aqueous reduction of .alpha.,.beta.-unsaturated aldehydes", XP002685178, retrieved from STN Database accession no. 2007:1473654 *
DATABASE CA [online] CHEMICAL ABSTRACTS SERVICE, COLUMBUS, OHIO, US; CHEN, JIAN ET AL: "A practical and mild method for the highly selective conversion of terminal alkenes into aldehydes through epoxidation-isomerization with ruthenium(IV)-porphyrin catalysts", XP002685177, retrieved from STN Database accession no. 2004:809517 *
DATABASE CA [online] CHEMICAL ABSTRACTS SERVICE, COLUMBUS, OHIO, US; CHOUDARY, B. M. ET AL: "The first example of activation of molecular oxygen by nickel in Ni-Al hydrotalcite: a novel protocol for the selective oxidation of alcohols", XP002685176, retrieved from STN Database accession no. 2001:169964 *
DATABASE CA [online] CHEMICAL ABSTRACTS SERVICE, COLUMBUS, OHIO, US; DENMARK, SCOTT E. ET AL: "On the Mechanism of the Selenolactonization Reaction with Selenenyl Halides", XP002685175, retrieved from STN Database accession no. 2006:826279 *
DATABASE CA [online] CHEMICAL ABSTRACTS SERVICE, COLUMBUS, OHIO, US; DURAND, MARC HENRI: ".beta.-Acetylenic aldehydes and their derivatives: ethoxy enynes and acetals", XP002658129, retrieved from STN Database accession no. 1963:14507 *
DATABASE CA [online] CHEMICAL ABSTRACTS SERVICE, COLUMBUS, OHIO, US; OHNO, HIROAKI ET AL: "Samarium(II)-Promoted Radical Spirocyclization onto an Aromatic Ring", XP002685186, retrieved from STN Database accession no. 2003:679383 *
DATABASE CA [online] CHEMICAL ABSTRACTS SERVICE, COLUMBUS, OHIO, US; PARRAIN, JEAN LUC ET AL: "An efficient access to homoallyl and homocinnamyl skeletons using 1-(tributylstannyl)-4,4-diethoxy-1-butene", XP002658130, retrieved from STN Database accession no. 1990:496681 *
DATABASE CA [online] CHEMICAL ABSTRACTS SERVICE, COLUMBUS, OHIO, US; PINNICK, HAROLD W.: "The Nef reaction", XP002685181, retrieved from STN Database accession no. 2008:1383585 *
DATABASE CA [online] CHEMICAL ABSTRACTS SERVICE, COLUMBUS, OHIO, US; VON ANGERER, S. ET AL: "Product class 6: acyclic and semicyclic O/O acetals", XP002685183, retrieved from STN Database accession no. 2007:839701 *
DATABASE CA [online] CHEMICAL ABSTRACTS SERVICE, COLUMBUS, OHIO, US; WU, HONGLIU: "Pemetrexed intermediate and its preparation", XP002685182, retrieved from STN Database accession no. 2007:1427648 *
DATABASE CA [online] CHEMICAL ABSTRACTS SERVICE, COLUMBUS, OHIO, US; ZARAGOZA, FLORENCIO ET AL: "Direct C-4 arylation of crotonaldehyde with arenediazonium tetrafluoroborates", XP002685185, retrieved from STN Database accession no. 2011:991995 *
DATABASE CA [online] CHEMICAL ABSTRACTS SERVICE, COLUMBUS, OHIO, US; ZUEND, STEPHAN J. ET AL: "Scaleable catalytic asymmetric Strecker syntheses of unnatural .alpha.-amino acids", XP002685179, retrieved from STN Database accession no. 2009:1349569 *
DENMARK, SCOTT E. ET AL: "On the Mechanism of the Selenolactonization Reaction with Selenenyl Halides", JOURNAL OF ORGANIC CHEMISTRY, vol. 71, no. 19, 2006, pages 7293 - 7306, XP055047973, ISSN: 0022-3263, DOI: doi:10.1021/jo0610457 *
KJELL D P ET AL: "A NOVEL, NONAQUEOUS METHOD FOR REGENERATION OF ALDEHYDES FROM BISULFITE ADDUCTS", JOURNAL OF ORGANIC CHEMISTRY, vol. 64, no. 15, 7 February 1999 (1999-02-07), AMERICAN CHEMICAL SOCIETY, EASTON.; US, pages 5722 - 5724, XP003013995, ISSN: 0022-3263, DOI: 10.1021/JO990543V *
OHNO, HIROAKI ET AL: "Samarium(II)-Promoted Radical Spirocyclization onto an Aromatic Ring", JOURNAL OF ORGANIC CHEMISTRY, vol. 68, no. 20, 2003, pages 7722 - 7732, XP055047991, ISSN: 0022-3263, DOI: doi:10.1021/jo034767w *
PINNICK, HAROLD W.: "The Nef reaction", ORGANIC REACTIONS (HOBOKEN, NJ, UNITED STATES) , 38, NO PP. GIVEN CODEN: ORHNBA URL:, 1990 *
TETRAHEDRON LETTERS, vol. 31, no. 13, 1990, pages 1857 - 1860, ISSN: 0040-4039 *
VON ANGERER, S. ET AL: "Product class 6: acyclic and semicyclic O/O acetals", SCIENCE OF SYNTHESIS, vol. 29, 2007, pages 303 - 406 *
ZARAGOZA, FLORENCIO ET AL: "Direct C-4 arylation of crotonaldehyde with arenediazonium tetrafluoroborates", TETRAHEDRON LETTERS, vol. 52, no. 36, 2011, pages 4678 - 4680, XP028252783, ISSN: 0040-4039, DOI: doi:10.1016/j.tetlet.2011.07.005 *
ZUEND, STEPHAN J. ET AL: "Scaleable catalytic asymmetric Strecker syntheses of unnatural .alpha.-amino acids", NATURE (LONDON, UNITED KINGDOM) , 461, 968-970 CODEN: NATUAS; ISSN: 0028-0836, 7266 *

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WO2012150280A2 (en) 2012-11-08

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