WO2015113903A1 - Verfahren zur herstellung von 1-indanolen und 1-indanaminen - Google Patents

Verfahren zur herstellung von 1-indanolen und 1-indanaminen Download PDF

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Publication number
WO2015113903A1
WO2015113903A1 PCT/EP2015/051344 EP2015051344W WO2015113903A1 WO 2015113903 A1 WO2015113903 A1 WO 2015113903A1 EP 2015051344 W EP2015051344 W EP 2015051344W WO 2015113903 A1 WO2015113903 A1 WO 2015113903A1
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Prior art keywords
hydrogen
alkyl
methyl
cor
palladium
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Ceased
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PCT/EP2015/051344
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German (de)
English (en)
French (fr)
Inventor
Mark James Ford
Jean-Pierre Vors
Olivier Baudoin
Simon JANODY
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Bayer CropScience AG
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Bayer CropScience AG
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Priority to MX2016009839A priority Critical patent/MX362690B/es
Priority to ES15701198.2T priority patent/ES2657797T3/es
Priority to US15/114,385 priority patent/US9796737B2/en
Priority to KR1020167022941A priority patent/KR102362143B1/ko
Priority to DK15701198.2T priority patent/DK3099671T3/da
Priority to CN201580005701.7A priority patent/CN106414420B/zh
Priority to BR112016017513-1A priority patent/BR112016017513B1/pt
Priority to JP2016565561A priority patent/JP6475265B2/ja
Priority to EP15701198.2A priority patent/EP3099671B1/de
Application filed by Bayer CropScience AG filed Critical Bayer CropScience AG
Publication of WO2015113903A1 publication Critical patent/WO2015113903A1/de
Priority to IL246831A priority patent/IL246831B/en
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
    • C07F7/02—Silicon compounds
    • C07F7/08—Compounds having one or more C—Si linkages
    • C07F7/0803—Compounds with Si-C or Si-Si linkages
    • C07F7/081—Compounds with Si-C or Si-Si linkages comprising at least one atom selected from the elements N, O, halogen, S, Se or Te
    • 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
    • B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
    • B01J23/38—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals
    • B01J23/40—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals of the platinum group metals
    • B01J23/44—Palladium
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C209/00—Preparation of compounds containing amino groups bound to a carbon skeleton
    • C07C209/54—Preparation of compounds containing amino groups bound to a carbon skeleton by rearrangement reactions
    • C07C209/58—Preparation of compounds containing amino groups bound to a carbon skeleton by rearrangement reactions from or via amides
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C211/00—Compounds containing amino groups bound to a carbon skeleton
    • C07C211/33—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to carbon atoms of rings other than six-membered aromatic rings
    • C07C211/39—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to carbon atoms of rings other than six-membered aromatic rings of an unsaturated carbon skeleton
    • C07C211/41—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to carbon atoms of rings other than six-membered aromatic rings of an unsaturated carbon skeleton containing condensed ring systems
    • C07C211/42—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to carbon atoms of rings other than six-membered aromatic rings of an unsaturated carbon skeleton containing condensed ring systems with six-membered aromatic rings being part of the condensed ring systems
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C67/00—Preparation of carboxylic acid esters
    • C07C67/28—Preparation of carboxylic acid esters by modifying the hydroxylic moiety of the ester, such modification not being an introduction of an ester group
    • C07C67/297—Preparation of carboxylic acid esters by modifying the hydroxylic moiety of the ester, such modification not being an introduction of an ester group by splitting-off hydrogen or functional groups; by hydrogenolysis of functional groups
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
    • C07C69/02—Esters of acyclic saturated monocarboxylic acids having the carboxyl group bound to an acyclic carbon atom or to hydrogen
    • C07C69/22—Esters of acyclic saturated monocarboxylic acids having the carboxyl group bound to an acyclic carbon atom or to hydrogen having three or more carbon atoms in the acid moiety
    • C07C69/24—Esters of acyclic saturated monocarboxylic acids having the carboxyl group bound to an acyclic carbon atom or to hydrogen having three or more carbon atoms in the acid moiety esterified with monohydroxylic compounds
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
    • C07C69/62—Halogen-containing esters
    • C07C69/63—Halogen-containing esters of saturated acids
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/44—Iso-indoles; Hydrogenated iso-indoles
    • C07D209/48—Iso-indoles; Hydrogenated iso-indoles with oxygen atoms in positions 1 and 3, e.g. phthalimide
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
    • C07F7/02—Silicon compounds
    • C07F7/08—Compounds having one or more C—Si linkages
    • C07F7/18—Compounds having one or more C—Si linkages as well as one or more C—O—Si linkages
    • C07F7/1804—Compounds having Si-O-C linkages
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
    • C07F7/02—Silicon compounds
    • C07F7/08—Compounds having one or more C—Si linkages
    • C07F7/18—Compounds having one or more C—Si linkages as well as one or more C—O—Si linkages
    • C07F7/1804—Compounds having Si-O-C linkages
    • C07F7/1872—Preparation; Treatments not provided for in C07F7/20
    • 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
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2523/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00
    • C07C2523/38—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00 of noble metals
    • C07C2523/40—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00 of noble metals of the platinum group metals
    • C07C2523/44—Palladium
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2602/00—Systems containing two condensed rings
    • C07C2602/02—Systems containing two condensed rings the rings having only two atoms in common
    • C07C2602/04—One of the condensed rings being a six-membered aromatic ring
    • C07C2602/08—One of the condensed rings being a six-membered aromatic ring the other ring being five-membered, e.g. indane

Definitions

  • the invention relates to a process for the preparation of 1-indanols and 1 - indanamines by palladium-catalyzed arylation and their use as intermediates for the synthesis of fine chemicals and agrochemical active ingredients.
  • 1-indanols and 1-indanamines of the formula (I) in which Y represents a substituted hydroxyl or amino group, represent an important structural element in a large number of agronomically active substances, as described, for example, in WO 2004/069814 A1 and WO 2007 / 1 12834 A1.
  • Hui Fang et al . "Rapid Catalyst Screening by a Continuous Flow Microreactor Interfaced with Ultra High Pressure Liquid Chromatography," The Journal of Organic Chemistry
  • the object of the present invention is to provide a process for the preparation of 1-indanols and 1-indanamines which overcomes the disadvantages of the processes known from the prior art.
  • 1-indanols and 1-indanamines can be prepared in high yields by palladium-catalyzed arylation of 1- (2-halophenyl) alkane-1-ols or 1- (2-halophenyl) alkane-1 - amines.
  • An object of the present invention is thus a process for the preparation of 1-indanols and 1-indanamines of the general formula (I), characterized in that 1- (2-halo-phenyl) alkan-1-ols or 1- (2-halophenyl alkane-1-amine (II)
  • Y is NR 1 R 2 or OR 3 ,
  • R 1 is hydrogen or COR 4 ,
  • R 2 is COR 4 ,
  • R 1 and R 2 together form the group COCH 2 CH 2 CO or CO-phenylene-CO
  • R 3 is Si (R 5 ) 3 or pivaloyl (2,2-dimethylpropanoyl),
  • R 4 is (C 1 -C 6) -alkyl or phenyl
  • R 5 is (C 1 -C 6) -alkyl or phenyl
  • Hai means chlorine, bromine or iodine
  • R is fluorine, (C 1 -C 3 ) -alkyl or (C 1 -C 3 ) -alkoxy,
  • X 1 is hydrogen or (C 1 -C 6 ) -alkyl
  • X 2 is hydrogen or (C 1 -C 6 ) -alkyl
  • X 3 is hydrogen or (C 1 -C 6 ) -alkyl
  • X 4 is hydrogen or (C 1 -C 6 ) -alkyl
  • Y and X 1 together with the carbon atoms to which they are attached form a 5- to 7-membered saturated ring, m is 0, 1, 2 or 3.
  • Suitable palladium catalysts are, for example, Pd (OAc) 2, Pd2dba3
  • the palladium catalyst is usually used in an amount of 0.1 to 10 mol%, preferably 1 to 10 mol%, particularly preferably 1 to 5 mol%, based on the compound (II).
  • Suitable phosphine ligands are, for example, trialkylphosphines,
  • Tricycloalkylphosphines such as tricyclohexylphosphine, triarylphosphines such as
  • the phosphines can also be used in the form of salts, for example with HBF 4 .
  • the phosphine ligands are usually used in an amount of 0.1 to 10 mol%, preferably 1 to 10 mol%, particularly preferably 1 to 5 mol%, based on the compound (II).
  • Palladium catalysts and phosphine ligands may be used as separate compounds, or conveniently in the form of a preformed complex, e.g. as tretrakis (triphenylphosphinyl) palladium, which is particularly preferred.
  • Suitable bases are, for example, carbonates, bicarbonates, phosphates, alkoxides and carboxylates of alkali metals, such as L12CO3, Na2CO3, K2CO3, NaHCO3, KHCO3, K 3 PO 4, K 2 HPO 4, NaOMe, NaOEt, NaOiPr, NaOtBu, KOMe, KOEt, KOiPr, KOtBu, NaOAc, KOAc, NaOPiv (sodium pivalate), KOPiv, NaOCOPh and KOCOPh or mixtures of such bases.
  • Preference is given to mixtures of carbonates and carboxylates. Particularly preferred is the mixture of K2CO3 and KOPiv.
  • the base is usually used in a 1 to 5 molar ratio based on the compound (II).
  • Suitable solvents include, for example, aromatics such as toluene, xylene, chlorobenzene and anisole; Ethers such as dibutyl ether, diphenyl ether and polyglycol ether; Esters such as butyl acetate and isopropyl acetate; Amides such as dimethylacetamide, dimethylformamide, and dibutylformamide or mixtures thereof.
  • aromatic solvents such as xylene.
  • the preparation process of the invention is usually carried out at elevated temperature of about 100 ° C to the boiling point of the respective solvent.
  • Preferred is a range of 120 to 150 ° C. If the boiling point of the particular solvent should be below, it is expedient to work under pressure.
  • R 1 means
  • R 2 means
  • R 3 means
  • R 4 means
  • R 5 means
  • R means
  • Y and X 1 together with the carbon atoms to which they are attached form a 5- to 7-membered saturated ring, m is 0, 1, 2 or 3.
  • alkyl radicals having more than two carbon atoms may be straight-chain or branched.
  • Alkyl radicals mean e.g. Methyl, ethyl, n- or i-propyl, n-, i-, t- or 2-butyl, pentyls, hexyls, such as n-hexyl, i-hexyl and 1, 3-dimethylbutyl.
  • the palladium catalyst (0.015 mmol, 5 mol%)
  • the phosphine ligand (0.03 mmol, 10 mol%) and the base, for example, potassium pivalate (0.030 mmol, 10 mol%) and K 2 CO 3 (0.3 mmol, 1, 0 eq.) Submitted and the Solvent (3 ml of xylene) and a compound of formula (II) (0.3 mmol, 1 .0 eq.) Was added.
  • the mixture is then stirred for 10 minutes at room temperature and then heated to 140 ° C and stirred for 16 hours at this temperature. After cooling the reaction mixture to room temperature, the mixture is filtered, the solvent is stripped off and the residue is purified by chromatography.
  • Example 1 Preparation of 2,2-dimethyl-2,3-dihydro-1H-inden-1-yl) oxy) triisopropylsilane from [1- (2-bromophenyl) -2,2-dimethylpropoxy] (triisopropyl) silane
  • Example 2 Preparation of ((2 ', 3'-dihydrospiro [cyclopropane-1,1'-inden-3'-yl) oxy) triisopropylsilane from [1- (2-bromophenyl) -cyclopropylethoxy] (triisopropyl) silane
  • Example 3 Preparation of ((5,6-dimethoxy-2,2-dimethyl-2,3-dihydro-1H-inden-1-yl) oxy) triisopropylsilane from [1- (2-bromo-4,5-) dimethoxyphenyl) -2,2-dimethylpropoxy] (tri-tert-butyl) silane
  • Example 4 Preparation of ((6-methoxy-2,2-dimethyl-2,3-dihydro-1H-inden-1-yl) oxy) triisopropylsilane from [1- (2-bromo-5-methoxyphenyl) -2 , 2-dimethylpropoxy] (tri-tert-butyl) silane
  • Example 5 Preparation of ((6-Fluoro-2,2-dimethyl-2,3-dihydro-1H-inden-1-yl) oxy) triisopropylsilane from [1- (2-bromo-5-fluorophenyl) -2 , 2-dimethylpropoxy] (tri-tert-butyl) silane
  • Example 7 Preparation of 6-methoxy-2,2-dimethyl-2,3-dihydro-1H-inden-1-yl-2,2-dimethylpropanoate from 1- (2-bromo-5-methoxyphenyl) -2, 2-dimethylpropyl-2,2-dimethylpropanoate
  • Example 8 Preparation of 6-fluoro-2,2-dimethyl-2,3-dihydro-1H-inden-1-yl-2,2-dimethylpropanoate from 1- (2-bromo-5-fluorophenyl) -2, 2-dimethylpropyl-2,2-dimethylpropanoate
  • Example 1 Preparation of 2- (2,2-dimethyl-2,3-dihydro-1H-inden-1-yl) isoindoline-1,3-dione from 2- [1- (2-bromophenyl) -2 , 2-dimethylpropyl] -1H-isoindole-1,3-2H-dione
  • Example 12 Preparation of (1R, 2S) -2,6-dimethylindan-1-mannin from 2- [1- (2-bromo-5-methylphenyl) -2-methylpropyl] -1H-isoindole-1,3 (2H) -dione via 2 - [(1R, 2S) -2,6-dimethyl-2,3-dihydro-1H-inden-1-yl] -1H-isoindole-1,3 (2H) - dion
  • Example 13 Preparation of triisopropyl ((2-methyl-2,3-dihydro-1H-inden-1-yl) oxy) silane from [1- (2-bromophenyl) -2-methylpropoxy] (triisopropyl) silane This reaction was carried out with various palladium catalysts, phosphine ligands and amounts of bases. The results obtained under different conditions are listed in tabular form:

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Catalysts (AREA)
  • Indole Compounds (AREA)
  • Furan Compounds (AREA)
PCT/EP2015/051344 2014-01-28 2015-01-23 Verfahren zur herstellung von 1-indanolen und 1-indanaminen Ceased WO2015113903A1 (de)

Priority Applications (10)

Application Number Priority Date Filing Date Title
JP2016565561A JP6475265B2 (ja) 2014-01-28 2015-01-23 １−インダノールおよび１−インダンアミンを製造する方法
ES15701198.2T ES2657797T3 (es) 2014-01-28 2015-01-23 Procedimiento para producir 1-indanoles y 1-indanaminas
US15/114,385 US9796737B2 (en) 2014-01-28 2015-01-23 Method for producing 1-indanoles and 1-indanamines
KR1020167022941A KR102362143B1 (ko) 2014-01-28 2015-01-23 1-인다놀 및 1-인단아민의 제조방법
DK15701198.2T DK3099671T3 (da) 2014-01-28 2015-01-23 Fremgangsmåde til fremstilling af 1-indanoler og 1-indanaminer
MX2016009839A MX362690B (es) 2014-01-28 2015-01-23 Metodo para producir 1-indanoles y 1-indanaminas.
BR112016017513-1A BR112016017513B1 (pt) 2014-01-28 2015-01-23 Processo para preparação de 1-indanóis e 1-indanaminas
CN201580005701.7A CN106414420B (zh) 2014-01-28 2015-01-23 制备1-茚满醇和1-茚满胺的方法
EP15701198.2A EP3099671B1 (de) 2014-01-28 2015-01-23 Verfahren zur herstellung von 1-indanolen und 1-indanaminen
IL246831A IL246831B (en) 2014-01-28 2016-07-19 A method for the production of 1-indanols and 1-indanamines

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP14152790 2014-01-28
EP14152790.3 2014-01-28

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US (1) US9796737B2 (enExample)
EP (1) EP3099671B1 (enExample)
JP (1) JP6475265B2 (enExample)
KR (1) KR102362143B1 (enExample)
CN (1) CN106414420B (enExample)
BR (1) BR112016017513B1 (enExample)
DK (1) DK3099671T3 (enExample)
ES (1) ES2657797T3 (enExample)
IL (1) IL246831B (enExample)
MX (1) MX362690B (enExample)
TW (1) TWI668201B (enExample)
WO (1) WO2015113903A1 (enExample)

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CN113797978B (zh) * 2021-10-12 2023-11-07 青岛科技大学 一类聚三芳基氧膦负载钯/铜双金属催化剂的制备方法及应用

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Publication number Priority date Publication date Assignee Title
WO2024201469A1 (en) 2023-03-29 2024-10-03 Adama Agan Ltd. Process for the preparation of amine intermediates

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MX362690B (es) 2019-02-01
BR112016017513A2 (enExample) 2017-08-08
EP3099671A1 (de) 2016-12-07
US20160340370A1 (en) 2016-11-24
JP6475265B2 (ja) 2019-02-27
BR112016017513B1 (pt) 2022-03-03
KR20160113643A (ko) 2016-09-30
TW201613843A (en) 2016-04-16
ES2657797T3 (es) 2018-03-06
IL246831B (en) 2018-11-29
EP3099671B1 (de) 2017-12-27
US9796737B2 (en) 2017-10-24
CN106414420B (zh) 2018-12-14
DK3099671T3 (da) 2018-01-29
JP2017508783A (ja) 2017-03-30
KR102362143B1 (ko) 2022-02-10
MX2016009839A (es) 2016-10-31
CN106414420A (zh) 2017-02-15
TWI668201B (zh) 2019-08-11

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