AR043515A1 - Procedimiento para preparar derivados quirales beta aminoacidos mediante hidrogenacion asimetrica - Google Patents

Procedimiento para preparar derivados quirales beta aminoacidos mediante hidrogenacion asimetrica

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Publication number
AR043515A1
AR043515A1 ARP040100745A ARP040100745A AR043515A1 AR 043515 A1 AR043515 A1 AR 043515A1 AR P040100745 A ARP040100745 A AR P040100745A AR P040100745 A ARP040100745 A AR P040100745A AR 043515 A1 AR043515 A1 AR 043515A1
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AR
Argentina
Prior art keywords
alkyl
aryl
ring system
structural formula
heterocyclic ring
Prior art date
Application number
ARP040100745A
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English (en)
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Merck & Co Inc
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First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=33098076&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=AR043515(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Merck & Co Inc filed Critical Merck & Co Inc
Publication of AR043515A1 publication Critical patent/AR043515A1/es

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    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/16Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
    • B01J31/22Organic complexes
    • B01J31/2282Unsaturated compounds used as ligands
    • B01J31/2295Cyclic compounds, e.g. cyclopentadienyls
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/16Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
    • B01J31/24Phosphines, i.e. phosphorus bonded to only carbon atoms, or to both carbon and hydrogen atoms, including e.g. sp2-hybridised phosphorus compounds such as phosphabenzene, phosphole or anionic phospholide ligands
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/16Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
    • B01J31/24Phosphines, i.e. phosphorus bonded to only carbon atoms, or to both carbon and hydrogen atoms, including e.g. sp2-hybridised phosphorus compounds such as phosphabenzene, phosphole or anionic phospholide ligands
    • B01J31/2404Cyclic ligands, including e.g. non-condensed polycyclic ligands, the phosphine-P atom being a ring member or a substituent on the ring
    • B01J31/2409Cyclic ligands, including e.g. non-condensed polycyclic ligands, the phosphine-P atom being a ring member or a substituent on the ring with more than one complexing phosphine-P atom
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C227/00Preparation of compounds containing amino and carboxyl groups bound to the same carbon skeleton
    • C07C227/14Preparation of compounds containing amino and carboxyl groups bound to the same carbon skeleton from compounds containing already amino and carboxyl groups or derivatives thereof
    • C07C227/16Preparation of compounds containing amino and carboxyl groups bound to the same carbon skeleton from compounds containing already amino and carboxyl groups or derivatives thereof by reactions not involving the amino or carboxyl groups
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C231/00Preparation of carboxylic acid amides
    • C07C231/12Preparation of carboxylic acid amides by reactions not involving the formation of carboxamide groups
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C231/00Preparation of carboxylic acid amides
    • C07C231/16Preparation of optical isomers
    • C07C231/18Preparation of optical isomers by stereospecific synthesis
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic 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
    • C07D487/04Ortho-condensed systems
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2231/00Catalytic reactions performed with catalysts classified in B01J31/00
    • B01J2231/60Reduction reactions, e.g. hydrogenation
    • B01J2231/64Reductions in general of organic substrates, e.g. hydride reductions or hydrogenations
    • B01J2231/641Hydrogenation of organic substrates, i.e. H2 or H-transfer hydrogenations, e.g. Fischer-Tropsch processes
    • B01J2231/645Hydrogenation of organic substrates, i.e. H2 or H-transfer hydrogenations, e.g. Fischer-Tropsch processes of C=C or C-C triple bonds
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2531/00Additional information regarding catalytic systems classified in B01J31/00
    • B01J2531/02Compositional aspects of complexes used, e.g. polynuclearity
    • B01J2531/0261Complexes comprising ligands with non-tetrahedral chirality
    • B01J2531/0263Planar chiral ligands, e.g. derived from donor-substituted paracyclophanes and metallocenes or from substituted arenes
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2531/00Additional information regarding catalytic systems classified in B01J31/00
    • B01J2531/02Compositional aspects of complexes used, e.g. polynuclearity
    • B01J2531/0286Complexes comprising ligands or other components characterized by their function
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2531/00Additional information regarding catalytic systems classified in B01J31/00
    • B01J2531/80Complexes comprising metals of Group VIII as the central metal
    • B01J2531/82Metals of the platinum group
    • B01J2531/822Rhodium
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2531/00Additional information regarding catalytic systems classified in B01J31/00
    • B01J2531/80Complexes comprising metals of Group VIII as the central metal
    • B01J2531/84Metals of the iron group
    • B01J2531/842Iron

Abstract

La presente se refiere a un procedimiento para la preparación eficiente de derivados beta aminoácidos enantioméricamente enriquecidos que son útiles en la síntesis asimétrica de moléculas biológicamente activas. Reivindicación 1: Un procedimiento para preparar un compuesto de fórmula estructural (1) que tiene la configuración ( R ) o (S) en el centro estereogénico marcado con un *; en un exceso enantiomérico de al menos un 70% por encima del enantiómero opuesto, en el que Z es OR2, SR2, o NR2R3; R1 es alquilo C1-8, arilo, heteroarilo, alquil C1-2-arilo, o alquil C1-2-heteroarilo; R2 y R3 son cada uno independientemente H, alquilo C1-8, arilo, o alquil C1-2-arilo, o R2 y R3 conjuntamente con el átomo de N al cual están unidos forman un sistema anular heterocíclico de 4 a 7 miembros que contiene opcionalmente un heteroátomo adicional seleccionado de O, S, y alquilo C1-4 N, estando dicho sistema anular heterocíclico condensado opcionalmente con un sistema anillo carbocíclico de 5 a 6 miembros saturado o aromático o un sistema anillo heterocíclico de 5 a 6 miembros saturado o aromático que contiene uno o dos heteroátomos seleccionados de O, S, y alquilo C1-4N, estando dicho sistema anillo fusionado no sustituido o sustituido con uno o dos sustituyentes seleccionados independientemente de hidroxi, amino, F, alquilo C1-4, alcoxi C1-4, y trifluorometilo; que comprende la etapa de hidrogenar una enamina proquiral de fórmula estructural (2) en un disolvente orgánico adecuado en presencia de un metal de transición precursor complejado con un ligando quiral ferrocenil difosfina de fórmula estructural (3) en la que R4 es alquilo C1-4 o arilo; R5 y R6 son cada uno de ellos independientemente alquilo C1-6, cicloalquilo C5-12, o arilo; y R7 es alquilo C1-4 o fenilo no sustituido.
ARP040100745A 2003-03-19 2004-03-09 Procedimiento para preparar derivados quirales beta aminoacidos mediante hidrogenacion asimetrica AR043515A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US45593203P 2003-03-19 2003-03-19

Publications (1)

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AR043515A1 true AR043515A1 (es) 2005-08-03

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ID=33098076

Family Applications (2)

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ARP040100745A AR043515A1 (es) 2003-03-19 2004-03-09 Procedimiento para preparar derivados quirales beta aminoacidos mediante hidrogenacion asimetrica
ARP090102853A AR072877A2 (es) 2003-03-19 2009-07-27 Una forma cristalina de (2r) -4-oxo-4-[3- (trifluorometil ) -5,6-dihidro -.[1,2,4 ] - triazolo [4,3-a ] pirazin-7 (8h ) -il] -1- (2,4,5,-trifluoro fenil ) butan -2-amina

Family Applications After (1)

Application Number Title Priority Date Filing Date
ARP090102853A AR072877A2 (es) 2003-03-19 2009-07-27 Una forma cristalina de (2r) -4-oxo-4-[3- (trifluorometil ) -5,6-dihidro -.[1,2,4 ] - triazolo [4,3-a ] pirazin-7 (8h ) -il] -1- (2,4,5,-trifluoro fenil ) butan -2-amina

Country Status (12)

Country Link
US (1) US7468459B2 (es)
EP (1) EP1606243B1 (es)
JP (3) JP4503594B2 (es)
CN (1) CN100339354C (es)
AR (2) AR043515A1 (es)
AT (1) ATE400545T1 (es)
AU (2) AU2004223885B2 (es)
CA (1) CA2518435C (es)
DE (1) DE602004014910D1 (es)
ES (1) ES2307000T3 (es)
TW (1) TWI312772B (es)
WO (1) WO2004085378A1 (es)

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US7468459B2 (en) 2008-12-23
US20060194977A1 (en) 2006-08-31
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CA2518435A1 (en) 2004-10-07
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CN100339354C (zh) 2007-09-26
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