RU2016106368A - Способ получения производного эндо-9-азабицикло[3.3.1]нонан-3-ола - Google Patents

Способ получения производного эндо-9-азабицикло[3.3.1]нонан-3-ола Download PDF

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RU2016106368A
RU2016106368A RU2016106368A RU2016106368A RU2016106368A RU 2016106368 A RU2016106368 A RU 2016106368A RU 2016106368 A RU2016106368 A RU 2016106368A RU 2016106368 A RU2016106368 A RU 2016106368A RU 2016106368 A RU2016106368 A RU 2016106368A
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Масая АКАСИ
Цутому ИНОУЕ
Хирохито ОООКА
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Ниппон Сода Ко., Лтд.
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    • 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
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    • B01J31/1805—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes containing nitrogen, phosphorus, arsenic or antimony as complexing atoms, e.g. in pyridine ligands, or in resonance therewith, e.g. in isocyanide ligands C=N-R or as complexed central atoms the ligands containing nitrogen
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    • B01J31/1805—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes containing nitrogen, phosphorus, arsenic or antimony as complexing atoms, e.g. in pyridine ligands, or in resonance therewith, e.g. in isocyanide ligands C=N-R or as complexed central atoms the ligands containing nitrogen
    • B01J31/181—Cyclic ligands, including e.g. non-condensed polycyclic ligands, comprising at least one complexing nitrogen atom as ring member, e.g. pyridine
    • B01J31/1815—Cyclic ligands, including e.g. non-condensed polycyclic ligands, comprising at least one complexing nitrogen atom as ring member, e.g. pyridine with more than one complexing nitrogen atom, e.g. bipyridyl, 2-aminopyridine
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    • B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
    • B01J31/18—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes containing nitrogen, phosphorus, arsenic or antimony as complexing atoms, e.g. in pyridine ligands, or in resonance therewith, e.g. in isocyanide ligands C=N-R or as complexed central atoms
    • B01J31/189—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes containing nitrogen, phosphorus, arsenic or antimony as complexing atoms, e.g. in pyridine ligands, or in resonance therewith, e.g. in isocyanide ligands C=N-R or as complexed central atoms containing both nitrogen and phosphorus as complexing atoms, including e.g. phosphino moieties, in one at least bidentate or bridging ligand
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    • B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
    • B01J31/24—Phosphines, 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
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    • B01J31/2404—Cyclic ligands, including e.g. non-condensed polycyclic ligands, the phosphine-P atom being a ring member or a substituent on the ring
    • B01J31/2409—Cyclic 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
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    • B01J31/2404—Cyclic ligands, including e.g. non-condensed polycyclic ligands, the phosphine-P atom being a ring member or a substituent on the ring
    • B01J31/2442—Cyclic ligands, including e.g. non-condensed polycyclic ligands, the phosphine-P atom being a ring member or a substituent on the ring comprising condensed ring systems
    • B01J31/2447—Cyclic ligands, including e.g. non-condensed polycyclic ligands, the phosphine-P atom being a ring member or a substituent on the ring comprising condensed ring systems and phosphine-P atoms as substituents on a ring of the condensed system or on a further attached ring
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D451/00—Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof
    • C07D451/14—Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof containing 9-azabicyclo [3.3.1] nonane ring systems, e.g. granatane, 2-aza-adamantane; Cyclic acetals thereof
    • 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
    • B01J2231/60—Reduction reactions, e.g. hydrogenation
    • B01J2231/64—Reductions in general of organic substrates, e.g. hydride reductions or hydrogenations
    • B01J2231/641—Hydrogenation of organic substrates, i.e. H2 or H-transfer hydrogenations, e.g. Fischer-Tropsch processes
    • B01J2231/643—Hydrogenation of organic substrates, i.e. H2 or H-transfer hydrogenations, e.g. Fischer-Tropsch processes of R2C=O or R2C=NR (R= C, H)
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
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    • B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
    • B01J2531/80—Complexes comprising metals of Group VIII as the central metal
    • B01J2531/82—Metals of the platinum group
    • B01J2531/821—Ruthenium
    • 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

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Catalysts (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Pyridine Compounds (AREA)

Claims (18)

1. Способ получения соединения, представленного формулой (II), включающий реакцию соединения, представленного следующей формулой (I), с водородом в присутствии катализатора, состоящего из комплекса рутения.
Figure 00000001
в формулах (I) и (II), R представляет собой атом водорода, незамещенную или замещенную алкильную группу, незамещенную или замещенную аралкильную группу, или незамещенную или замещенную алкоксикарбонильную группу.
2. Способ по п. 1, отличающийся тем, что комплекс рутения представляет собой соединение, представленное следующей формулой: Ru(X)(Y)(Px)n(L) или Ru(X)(Y)(PN)2, в этих формулах X и Y каждый независимо представляет собой анионный лиганд, Px представляет собой фосфиновый лиганд, n составляет 1 или 2, L представляет собой лиганд, представленный следующей формулой (III), или диаминный лиганд, и PN представляет собой лиганд, представленный следующей формулой (IV):
Figure 00000002
в формулах R1 и R2 каждый независимо представляет собой атом водорода, незамещенную или замещенную алкильную группу, незамещенную или замещенную арильную группу, или незамещенную или замещенную аралкильную группу,
кольцо B представляет собой незамещенный или замещенный гетероцикл,
отрезок двойной линии, состоящей из непрерывной линии и штриховой линии, представляет собой одинарную связь или двойную связь,
Z представляет собой координирующий атом, выбранный из группы, которую составляют N, P, O и S,
R3 и R4 каждый независимо представляет собой незамещенную или замещенную алкильную группу, незамещенную или замещенную арильную группу, или незамещенную или замещенную аралкильную группу, и
A представляет собой незамещенную или замещенную C1-4-алкиленовую группу.
3. Способ по п. 2, отличающийся тем, что комплекс рутения представляет собой соединение, представленное формулой: Ru(X)(Y)(Px)n(L), и L представляет собой пиридин-2-илметанамин, (1-метил-1H-бензимидазол-2-ил)метанамин, (5-метилпиразин-2-ил) метанамин, бензоксазол-2-илметанамин, пиримидин-2-илметанамин, тиазол-2-илметанамин или (пиразин-2-ил)метанамин.
4. Способ по п. 2, отличающийся тем, чтокомплекс рутения представляет собой соединение, представленное формулой: Ru(X)(Y)(Px)n(L), и L представляет собой диаминный лиганд, представленный следующей формулой (VI):
Figure 00000003
в которой R5-R12 каждый независимо представляет собой атом водорода, незамещенную или замещенную алкильную группу, незамещенную или замещенную арильную группу, или незамещенную или замещенную аралкильную группу, два из R5-R12 могут соединяться друг с другом, образуя кольцо, D представляет собой одинарную связь, незамещенную или замещенную алкиленовую группу, незамещенную или замещенную циклоалкиленовую группу, незамещенную или замещенную ариленовую группу, или незамещенную или замещенную двухвалентную гетероциклическую группу.
5. Способ по п. 2, отличающийся тем, чтокомплекс рутения представляет собой соединение, представленное формулой: Ru(X)(Y)(PN)2, и PN представляет собой лиганд, представленный следующей формулой (V):
Figure 00000004
6. Способ по любому из пп. 1-5, отличающийся тем, чтов формулах (I) и (II) R представляет собой незамещенную или замещенную аралкильную группу, и незамещенная или замещенная аралкильная группа представляет собой бензильную группу.
RU2016106368A 2013-09-06 2014-08-14 Способ получения производного эндо-9-азабицикло[3.3.1]нонан-3-ола RU2639150C2 (ru)

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