Method for production of Δ1-pyrrolines

Abstract

2,5-Bisaryl-Δ1-pyrrolines of the formula (I)

Description

The present invention relates to a novel process for preparing 2,5-bisaryl-Δ¹-pyrrolines.

Δ¹-Pyrrolines, processes for their preparation and their use as pesticides are already described in WO 00/21958, WO 99/59968, WO 99/59967 and WO 98/22438. However, in terms of yield, practice of the reaction, the number of byproducts, the kind of work-up, the amount of waste produced and the energy requirements, these processes are unsatisfactory. Accordingly, there is a constant need for novel processes which overcome one or more of the disadvantages mentioned.

It has now been found that 2,5-bisaryl-Δ¹-pyrrolines of the formula (I)

in which

• Ar¹ represents the radical

• Ar² represents the radical

• m represents 1, 2, 3 or 4,
• R¹ represents halogen, cyano, nitro, alkyl, alkoxy, haloalkyl, haloalkoxy, alkoxyalkyl or —S(O)_oR⁶,
• R² and R³ independently of one another represent hydrogen, halogen, cyano, nitro, alkyl, alkoxy, haloalkyl, haloalkoxy, alkoxyalkyl or —S(O)_oR⁶,
• R⁴ represents halogen or one of the groupings below
  • (l) —X—A
  • (m) —B—Z—D
  • (n) —Y—E
• R⁵ represents hydrogen, halogen, hydroxyl, cyano, alkyl, alkylcarbonyl, alkoxy, haloalkyl, haloalkoxy, trialkylsilyl, alkoxycarbonyl, —CONR⁷R⁸, —OSO₂NR⁷R⁸ or —S(O)_oR⁶,
• X represents a direct bond, O (oxygen), S(O)_o, NR⁶, carbonyl, carbonyloxy, oxycarbonyl, oxysulfonyl (OSO₂), alkylene, alkenylene, alkynylene, alkylen-oxy, oxyalkylene, oxyalkylenoxy, thioalkylene, cyclopropylene or oxiranylene,
• A represents phenyl, naphthyl or tetrahydronaphthyl, each of which is optionally mono- or polysubstituted by radicals from the list W¹, or represents 5- to 10-membered saturated or unsaturated heterocyclyl which contains one or more heteroatoms from a group consisting of nitrogen, oxygen and sulfur and which is in each case optionally mono- or polysubstituted by radicals from the list W²,
• B represents p-phenylene which is optionally mono- or disubstituted by radicals from the list W¹,
• Z represents (CH₂)_n, O (oxygen) or S(O)_o,
• D represents hydrogen, alkyl, alkenyl, alkynyl, haloalkyl, haloalkenyl, alkoxycarbonyl, haloalkylsulfonyl or dialkylamninosulfonyl,
• Y represents a direct bond, O (oxygen), S (sulfur), SO₂, carbonyl, carbonyloxy, oxycarbonyl, alkylene, alkenylene, alkynylene, haloalkylene, haloalkenylene, alkylenoxy, oxyalkylene, oxyalkylenoxy or thioalkylene,
• E represents hydrogen, alkyl, alkenyl, alkynyl, haloalkyl, haloalkenyl, haloalkylsulfonyl, cycloalkyl, dialkylaminocarbonyl or dialkylaminosulfonyl,
• W¹ represents cyano, halogen, formyl, nitro, alkyl, trialkylsilyl, alkoxy, haloalkyl, haloalkoxy, haloalkenyloxy, haloalkylsulfonyloxy, alkylcarbonyl, alkoxycarbonyl, —S(O)_oR⁶, —SO₂NR⁷R⁸, or —OSO₂NR⁷R⁸,
• W² represents cyano, halogen, formyl, nitro, alkyl, trialkylsilyl, alkoxy, haloalkyl, haloalkoxy, haloalkenyloxy, haloalkenylsulfonyloxy, alkylcarbonyl, alkoxycarbonyl, —S(O)_oR⁶, —SO₂NR⁷R⁸, —OSO₂NR⁷R⁸ or —NR⁷R⁸,
• n represents 0, 1, 2, 3 or 4,
• o represents 0, 1 or 2,
• R⁶ represents hydrogen, alkyl or haloalkyl,
• R⁷ and R⁸ independently of one another represent hydrogen, alkyl, haloalkyl, or together represent alkylene, alkoxyalkylene or alkylthioalkylene,where the compounds of the formula (I) may, depending on the nature and the number of substituents, be present as geometrical and/or optical isomers, regioisomers or configurational isomers or isomer mixtures thereof of varying composition,can be prepared byreacting aroylpyrrolidinones of the formula (II)

in whichAr¹ and Ar² are as defined abovewith an acid, if appropriate in the presence of a diluent.

It is extremely surprising that 2,5-bisaryl-Δ¹-pyrrolines of the formula (I) can be prepared by the process according to the invention in a smooth reaction without interfering side reactions, in high yields and with high purity.

The process according to the invention is characterized by the following further advantage. Owing to the course of the reaction, the pyrrolines formed are obtained as only one double bond isomer with respect to the double bond in the pyrroline ring. The double bond in the ring is always located between the nitrogen atom and the carbon atom to which Ar¹ is attached. A possible shift of the C═C double bond has not been observed under the conditions of the process according to the invention.

Using tert-butyl 3-(2-bromobenzoyl)-2-oxo-5-[4-(trifluoromethoxy)phenyl]-1-pyrrolidinecarboxylate as starting material and sulfuric acid, the course of the process according to the invention can be illustrated by the formula scheme below.

The formula (II) provides a general definition of the amides required as starting materials for carrying out the process according to the invention.

Preferred substituents or ranges in the formulae of starting materials of the formula (II) shown above and below are illustrated below.

• Ar¹ preferably represents the radical

• Ar² preferably represents the radical

• m preferably represents 1, 2 or 3.
• R¹ preferably represents halogen, cyano, nitro, C₁-C₆-alkyl, C₁-C₆-alkoxy, C₁-C₆-haloalkyl, C₁-C₆-haloalkoxy, C₁-C₆-alkoxyalkyl or —S(O)_oR⁶.
• R² and R³ independently of one another preferably represent hydrogen, halogen, cyano, nitro, C₁-C₆-alkyl, C₁-C₆-alkoxy, C₁-C₆-haloalkyl, C₁-C₆-haloalkoxy, C₁-C₆-alkoxy-C₁-C₆-alkyl or —S(O)_oR⁶.
• R⁴ preferably represents fluorine, chlorine, bromine, iodine or one of the groupings below.
  • (l) —X—A
  • (m) —B—Z—D
  • (n) —Y—E
• R⁵ preferably represents hydrogen, halogen, hydroxyl, cyano, C₁-C₆-alkyl, C₁-C₆-alkylcarbonyl, C₁-C₆-alkoxy, C₁-C₆-haloalkyl, C₁-C₆-haloalkoxy, tri(C₁-C₆-alkyl)silyl, C₁-C₆-alkoxycarbonyl, —CONR⁷R⁸, —OSO₂NR⁷R⁸ or —S(O)_oR⁶.
• X preferably represents a direct bond, O (oxygen), S(O)_o, NR⁶, carbonyl, carbonyloxy, oxycarbonyl, oxysulfonyl (OSO₂), C₁-C₄-alkylene, C₂-C₄-alkenylene, C₂-C₄-alkynylene, C₁-C₄-alkylenoxy, C₁-C₄-oxyalkylene, C₁-C₄-oxyalkylenoxy, thio-C₁-C₄-alkylene, cyclopropylene or oxiranylene.
• A preferably represents phenyl, naphthyl or tetrahydronaphthyl, each of which is optionally mono- to tetrasubstituted by radicals from the list W¹, or represents 5- to 10-membered heterocyclyl which contains 1 or 2 aromatic rings and 1 to 4 heteroatoms, as a combination of 0 to 4 nitrogen atoms, 0 to 2 oxygen atoms and/or 0 to 2 sulfur atoms (in particular tetrazolyl, furyl, benzofuryl, thienyl, benzothienyl, pyrrolyl, indolyl, oxazolyl, benzoxazolyl, isoxazyl, imidazyl, pyrazyl, thiazolyl, benzothiazolyl, pyridyl, pyrimidinyl, pyridazyl, triazinyl, triazyl, quinolinyl or isoquinolinyl) and which is in each case optionally mono- to tetrasubstituted by radicals from the list W².
• B preferably represents p-phenylene which is optionally mono- or disubstituted by radicals from the list W¹.
• Z preferably represents (CH₂)_n, O (oxygen) or S(O)_o.
• D preferably represents hydrogen, C₁-C₆-alkyl, C₁-C₆-alkenyl, C₂-C₆-alkynyl, C₁-C₆-haloalkyl, C₂-C₆-haloalkenyl, C₁-C₆-alkoxycarbonyl, C₁-C₆-halo-alkylsulfonyl or di(C₁-C₆-alkyl)aminosulfonyl.
• Y preferably represents a direct bond, O (oxygen), S (sulfur), SO₂, carbonyl, carbonyloxy, oxycarbonyl, C₁-C₆-alkylene, C₂-C₆-alkenylene, C₂-C₆-alkynylene, C₁-C₆-haloalkylene, C₂-C₆-haloalkenylene, C₁-C₄-alkylenoxy, C₁-C₄-oxyalkylene, C₁-C₄-oxyalkylenoxy or thio-C₁-C₄-alkylene.
• E preferably represents hydrogen, C₁-C₆-alkyl, C₂-C₆-alkenyl, C₂-C₆-alkynyl, C₁-C₆-haloalkyl, C₂-C₆-haloalkenyl, C₁-C₆-haloalkylsulfonyl, C₃-C₇-cycloalkyl, di(C₁-C₆-alkyl)aminocarbonyl or di(C₁-C₆-alkyl)aminosulfonyl.
• W¹ preferably represents cyano, halogen, formyl, nitro, C₁-C₆-alkyl, C₁-C₄-tri-alkylsilyl, C₁-C₆-alkoxy, C₁-C₆-haloalkyl, C₁-C₆-haloalkoxy, C₂-C₆-halo-alkenyloxy, C₁-C₆-haloalkylsulfonyloxy, C₁-C₆-alkylcarbonyl, C₁-C₆-alkoxycarbonyl, —S(O)_oR⁶, —SO₂NR⁷R⁸ or —OSO₂NR⁷R⁸.
• W² preferably represents cyano, halogen, formyl, nitro, C₁-C₆-alkyl, tri(C₁-C₄-alkyl)silyl, C₁-C₆-alkoxy, C₁-C₆-haloalkyl, C₁-C₆-haloalkoxy, C₂-C₆-haloalkenyloxy, C₁-C₆-haloalkylsulfonyloxy, C₁-C₆-alkylcarbonyl, C₁-C₆-alkoxycarbonyl, —S(O)_oR⁶, —SO₂NR⁷R⁸, —OSO₂NR⁷R⁸ or —NR⁷R⁸.
• n preferably represents 0, 1, 2, 3 or 4.
• o preferably represents 0, 1 or 2.
• R⁶ preferably represents hydrogen, C₁-C₆-alkyl or C₁-C₆-haloalkyl.
• R⁷ and R⁸ independently of one another preferably represent hydrogen, C₁-C₆-alkyl, C₁-C₆-haloalkyl, or together represent C₂-C₆-alkylene, C₁-C₄-alkoxy-C₁-C₄-alkyl (for example morpholine) or C₁-C₄-alkylthio-C₁-C₄-alkyl (for example thiomorpholine).
• Ar¹ particularly preferably represents the radical

• Ar² particularly preferably represents the radical

• m particularly preferably represents 1 or 2.
• R¹ particularly preferably represents fluorine, chlorine, bromine, C₁-C₆-alkyl, C₁-C₆-alkoxy, C₁-C₆-haloalkyl having 1 to 13 fluorine and/or chlorine atoms or C₁-C₆-haloalkoxy having 1 to 13 fluorine and/or chlorine atoms.
• R² and R³ independently of one another particularly preferably represent hydrogen, fluorine, chlorine, bromine, C₁-C₆-alkyl, C₁-C₆-alkoxy, C₁-C₆-haloalkyl having 1 to 13 fluorine and/or chlorine atoms or C₁-C₆-haloalkoxy having 1 to 13 fluorine and/or chlorine atoms,
• R⁴ particularly preferably represents fluorine, chlorine, bromine, iodine or one of the groupings below
  • (l) —X—A
  • (m) —B—Z—D
  • (n) —Y—E
• R⁵ particularly preferably represents hydrogen, fluorine, chlorine, bromine, hydroxyl, cyano, C₁-C₆-alkyl, C₁-C₆-alkylcarbonyl, C₁-C₆-alkoxy, C₁-C₆-haloalkyl having 1 to 13 fluorine and/or chlorine atoms, C₁-C₆-haloalkoxy having 1 to 13 fluorine and/or chlorine atoms or —S(O)_oR⁶.
• X particularly preferably represents a direct bond, O (oxygen), S (sulfur), SO₂, carbonyl, carbonyloxy, oxycarbonyl, oxysulfonyl (OSO₂), C₁-C₄-alkylene, C₂-C₄-alkenylene, C₂-C₄-alkynylene, C₁-C₄-alkylenoxy, C₁-C₄-oxyalkylene, C₁-C₄-oxyalkylenoxy, thio-C₁-C₄-alkylene, cyclopropylene or oxiranylene.
• A particularly preferably represents phenyl, naphthyl or tetrahydronaphthyl, each of which is optionally mono- to trisubstituted by radicals from the list W¹, or represents 5- to 10-membered heterocyclyl which contains 1 or 2 aromatic rings and 1 to 4 heteroatoms, as a combination of 0 to 4 nitrogen atoms, 0 to 2 oxygen atoms and/or 0 to 2 sulfur atoms (in particular tetrazolyl, furyl, benzofuryl, thienyl, benzothienyl, pyrrolyl, indolyl, oxazolyl, benzoxazolyl, isoxazyl, imidazyl, pyrazyl, thiazolyl, benzothiazolyl, pyridyl, pyrimidinyl, pyridazyl, triazinyl, triazyl, quinolinyl or isoquinolinyl) and which is in each case optionally mono- to trisubstituted by radicals from the list W².
• B particularly preferably represents p-phenylene which is optionally mono- or disubstituted by radicals from the list W¹.
• Z particularly preferably represents (CH₂)_n, O (oxygen) or S(O)_o.
• D particularly preferably represents hydrogen, C₁-C₆-alkyl, C₁-C₆-alkenyl, C₂-C₆-alkynyl, C₁-C₆-haloalkyl having 1 to 13 fluorine and/or chlorine atoms, C₂-C₆-haloalkenyl having 1 to 11 fluorine and/or chlorine atoms, C₁-C₆-alkoxycarbonyl, C₁-C₆-haloalkylsulfonyl having 1 to 13 fluorine and/or chlorine atoms or di(C₁-C₄-alkyl)aminosulfonyl.
• Y particularly preferably represents a direct bond, O (oxygen), S (sulfur), SO₂, carbonyl, carbonyloxy, oxycarbonyl, C₁-C₆-alkylene, C₂-C₆-alkenylene, C₂-C₆-alkynylene, C₁-C₆-haloalkylene having 1 to 12 fluorine and/or chlorine atoms, C₂-C₆-haloalkenylene having 1 to 10 fluorine and/or chlorine atoms, C₁-C₄-alkylenoxy, C₁-C₄-oxyalkylene, C₁-C₄-oxyalkylenoxy or thio-C₁-C₄-alkylene.
• E particularly preferably represents hydrogen, C₁-C₆-alkyl, C₂-C₆-alkenyl, C₂-C₆-alkynyl, C₁-C₆-haloalkyl having 1 to 13 fluorine and/or chlorine atoms, C₂-C₆-haloalkenyl having 1 to 11 fluorine and/or chlorine atoms, C₁-C₆-haloalkylsulfonyl having 1 to 13 fluorine and/or chlorine atoms, C₃-C₆-cycloalkyl, di(C₁-C₆-alkyl)aminocarbonyl or di(C₁-C₆-alkyl)aminosulfonyl.
• W¹ particularly preferably represents fluorine, chlorine, bromine, C₁-C₄-alkyl, C₁-C₄-alkoxy, C₁-C₄-haloalkyl having 1 to 9 fluorine and/or chlorine atoms, C₁-C₄-haloalkoxy having 1 to 9 fluorine and/or chlorine atoms, C₁-C₄-alkyl-carbonyl, C₁-C₄-alkoxycarbonyl, —SO₂NR⁷R⁸ or —S(O)_oR⁶.
• W² particularly preferably represents fluorine, chlorine, bromine, C₁-C₄-alkyl, C₁-C₄-alkoxy, C₁-C₄-haloalkyl having 1 to 9 fluorine and/or chlorine atoms, C₁-C₄-haloalkoxy having 1 to 9 fluorine and/or chlorine atoms, C₂-C₆-haloalkenyloxy having 1 to 11 fluorine and/or chlorine atoms, C₁-C₄-alkylcarbonyl, C₁-C₄-alkoxycarbonyl, —SO₂NR⁷R⁸ or —S(O)_oR⁶.
• n particularly preferably represents 0, 1, 2 or 3.
• o particularly preferably represents 0, 1 or 2.
• R⁶ particularly preferably represents C₁-C₆-alkyl or represents methyl or ethyl, each of which is substituted by 1 to 5 fluorine and/or chlorine atoms.
• R⁷ and R⁸ independently of one another particularly preferably represent hydrogen, C₁-C₄-alkyl, C₁-C₄-haloalkyl having 1 to 9 fluorine, chlorine and/or bromine atoms, or together represent —(CH₂)₅—, —(CH₂)₄—, —(CH₂)₂—O—(CH₂)₂— or —(CH₂)₂—S—(CH₂)₂—.
• Ar¹ very particularly preferably represents the radical

• Ar² very particularly preferably represents the radical

• R¹ very particularly preferably represents fluorine, chlorine, bromine, methyl, ethyl, n-propyl, i-propyl, n-butyl, i-butyl, s-butyl, t-butyl, methoxy, ethoxy, n-propoxy, i-propoxy, n-butoxy, i-butoxy, s-butoxy, t-butoxy, trifluoromethyl or trifluoromethoxy.
• R² and R³ independently of one another very particularly preferably represent hydrogen, fluorine, chlorine, bromine, methyl, ethyl, n-propyl, i-propyl, n-butyl, i-butyl, s-butyl, t-butyl, methoxy, ethoxy, n-propoxy, i-propoxy, n-butoxy, i-butoxy, s-butoxy, t-butoxy, trifluoromethyl or trifluoromethoxy.
• R⁴ very particularly preferably represents fluorine, chlorine, bromine or one of the groupings below
  • (l) —X—A
  • (m) —B—Z—D
  • (n) —Y—E
• R⁵ very particularly preferably represents hydrogen, fluorine, chlorine, bromine, hydroxyl, methyl, ethyl, methoxy, ethoxy, i-propoxy, methylthio, ethylthio, trifluoromethyl, difluoromethoxy, trifluoromethoxy, trifluoromethylthio or —SO₂CF₃.
• X very particularly preferably represents a direct bond, O (oxygen), S (sulfur), SO₂, carbonyl, —CH₂—, —(CH₂)₂—, —CH═CH— (E or Z), —C≡C—, —CH₂O—, —(CH₂)₂O—, —OCH₂—, —SCH₂—, —S(CH₂)₂—, —OCH₂O— or —O(CH₂)₂O—.
• A very particularly preferably represents phenyl which is optionally mono- or disubstituted by radicals from the list W¹ or represents tetrazolyl, furyl, benzofuryl, thienyl, benzothienyl, pyrrolyl, indolyl, oxazolyl, benzoxazolyl, isoxazyl, imidazyl, pyrazyl, thiazolyl, benzothiazolyl, pyridyl, pyrimidinyl, pyridazyl, triazinyl or triazyl, each of which is optionally mono- or disubstituted by radicals from the list W².
• B very particularly preferably represents p-phenylene which is optionally monosubstituted by radicals from the list W¹.
• Z very particularly preferably represents O (oxygen), S (sulfur) or SO₂.
• D very particularly preferably represents hydrogen, methyl, ethyl, n-propyl, i-propyl, n-butyl, i-butyl, s-butyl, t-butyl, 2-propenyl, butenyl, propargyl, butynyl, —CF₃, —CHF₂, —CClF₂, —CF₂CHFCl, —CF₂CH₂F, —CF₂CCl₃, —CH₂CF₃, —CF₂CHFCF₃, —CH₂CF₂H, —CH₂CF₂CF₃, —CF₂CF₂H, —CF₂CHFCF₃, —CO₂Me, —CO₂Et, —SO₂CF₃, —SO₂(CF₂)₃CF₃, —SO₂NMe₂.
• Y very particularly preferably represents a direct bond, O (oxygen), S (sulfur), SO₂, carbonyl, —CH₂—, —(CH₂)₂—, —CH═CH— (E or Z), —C≡C—, —CH₂O—, —(CH₂)₂O—, —OCH₂—, —SCH₂—, —S(CH₂)₂—, —OCH₂O— or —O(CH₂)₂O—.
• E very particularly preferably represents hydrogen, methyl, ethyl, n-propyl, i-propyl, n-butyl, i-butyl, s-butyl, t-butyl, 2-propen-1-yl, butenyl, propargyl, butynyl, —CF₃, —CHF₂, —CClF₂, —CF₂CHFCl, —CF₂CH₂F, —CF₂CCl₃, —CH₂CF₃, —CF₂CHFCF₃, —CH₂CF₂H, —CH₂CF₂CF₃, —CF₂CF₂H, —CF₂CHFCF₃, —SO₂CF₃, —SO₂(CF₂)₃CF₃, cyclohexyl, dimethylaminocarbonyl, —SO₂NMe₂.
• W¹ very particularly preferably represents fluorine, chlorine, bromine, methyl, ethyl, n-propyl, i-propyl, n-butyl, i-butyl, s-butyl, t-butyl, methoxy, ethoxy, n-propoxy, i-propoxy, n-butoxy, i-butoxy, s-butoxy, t-butoxy, trifluoromethoxy, difluoromethoxy, —CF₃, —CHF₂, —CClF₂, —CF₂CHFCl, —CF₂CH₂F, —CF₂CCl₃, —CH₂CF₃, —CF₂CHFCF₃, —CH₂CF₂H, —CH₂CF₂CF₃, CF₂CF₂H, —CF₂CHFCF₃, —SCF₃, —SCHF₂, —SO₂CHF₂, —SO₂CF₃, —SO₂NMe₂, —COCH₃ or —SO₂Me₂.
• W² very particularly preferably represents fluorine, chlorine, bromine, methyl, ethyl, n-propyl, i-propyl, t-butyl, trifluoromethyl, trifluoromethoxy, difluoromethoxy, trifluoromethylthio, —COCH₃, —SO₂CF₃ or —SO₂NMe₂.

Particularly preferred starting materials for the process according to the invention are the compounds of the formula (II-a)

in which

• R¹ represents halogen, methyl, methoxy, trifluoromethyl or trifluoromethoxy,
• R² represents hydrogen or halogen,
• R⁴ represents phenyl which is mono- or disubstituted by radicals from the list W¹ or represents heterocyclyl which is mono- or disubstituted from the list W² or represents the grouping —Y—E,
• R⁵ represents hydrogen or alkoxy and
• Y, E, W¹ and W² have the meanings given above as general, preferred, particularly preferred and/or very particularly preferred.

Very particular preference is given to starting materials of the formula (II-a) in which

• R¹ represents fluorine, chlorine, methyl, methoxy, trifluoromethyl or trifluoromethoxy,
• R² represents hydrogen, fluorine or chlorine,
• R⁴ represents phenyl which is mono- or disubstituted by radicals from the list W¹ or represents heterocyclyl which is mono- or disubstituted from the list W² or represents the grouping —Y—E,
• R⁵ represents hydrogen or C₁-C₆-alkoxy and
• Y, E, W¹ and W² have the meanings given above as general, preferred, particularly preferred and/or very particularly preferred.

Especially preferred are starting materials of the formula (II-a) in which

• R¹ represents fluorine, chlorine, methyl, methoxy, trifluoromethyl or trifluoromethoxy,
• R² represents hydrogen, fluorine or chlorine,
• R⁴ represents phenyl which is mono- or disubstituted by radicals from the list W¹ or represents heterocyclyl which is mono- or disubstituted from the list W² or represents the grouping —Y—E,
• R⁵ represents hydrogen, methoxy or ethoxy and
• Y, E, W¹ and W² have the meanings given above as general, preferred, particularly preferred and/or very particularly preferred.

Starting materials for the process according to the invention which are likewise emphasized are the compounds of the formula (II-b)

in which

• Ar², R¹, R² and R³ are as defined above.

Starting materials for the process according to the invention which are likewise emphasized are the compounds of the formula (II-c)

in which

• Ar², R¹, R² and R³ are as defined above.

Preference is given to compounds of the formulae (II-b) and (II-c), in which Ar², R¹, R² and R³ have the meanings given above as being preferred for these radicals.

Particular preference is given to compounds of the formulae (II-b) and (II-c) in which Ar², R¹, R² and R³ have the meanings given above as being particularly preferred for these radicals.

Very particular preference is given to the compounds of the formulae (II-b) and (II-c) in which Ar², R¹, R² and R³ have the meanings given above as being very particularly preferred for these radicals.

Starting materials for the process according to the invention which are likewise emphasized are the compounds of the formula (II-d)

in whichAr¹, R⁴, R⁵ and m are as defined above.

Starting materials for the process according to the invention which are likewise emphasized are the compounds of the formula (II-e)

in whichAr¹, R⁴, R⁵ and m are as defined above.

Preference is given to compounds of the formulae (II-d) and (II-e), in which R¹, R², R³ and Ar² have the meanings given above as being preferred for these radicals.

Particular preference is given to the compounds of the formulae (II-d) and (II-e), in which R¹, R², R³ and Ar² have the meanings given above as being particularly preferred for these radicals.

Very particular preference is given to the compounds of the formulae (II-d) and (II-e) in which R¹, R², R³ and Ar² have the meanings given above as being very particularly preferred for these radicals.

Particularly preferred starting materials for the process according to the invention are the compounds of the formula (II-f)

in which

• R¹ represents halogen, methyl, methoxy, trifluoromethyl or trifluoromethoxy,
• R² represents hydrogen or halogen,
• R⁴ represents phenyl which is mono- or disubstituted by radicals from the list W¹ or represents heterocyclyl which is mono- or disubstituted from the list W² or represents the grouping —Y—E,
• R⁵ represents hydrogen or alkoxy and
• Y, E, W¹ and W² have the general, preferred, particularly preferred and/or very particularly preferred meanings given above.

Very particular preference is given to starting materials of the formula (II-f) in which

• R¹ represents fluorine, chlorine, methyl, methoxy, trifluoromethyl or trifluoromethoxy,
• R² represents hydrogen, fluorine or chlorine,
• R⁴ represents phenyl which is mono- or disubstituted by radicals from the list W¹ or represents heterocyclyl which is mono- or disubstituted from the list W² or represents the grouping —Y—E,
• R⁵ represents hydrogen or C₁-C₆-alkoxy and
• Y, E, W¹ and W² have the general, preferred, particularly preferred and/or very particularly preferred meanings given above.

Especially preferred are starting materials of the formula (II-f) in which

• R¹ represents fluorine, chlorine, methyl, methoxy, trifluoromethyl or trifluoromethoxy,
• R² represents hydrogen, fluorine or chlorine,
• R⁴ represents phenyl which is mono- or disubstituted by radicals from the list W¹ or represents heterocyclyl which is mono- or disubstituted from the list W² or represents the grouping —Y—E,
• R⁵ represents hydrogen, methoxy or ethoxy and
• Y, E, W¹ and W² have the general, preferred, particularly preferred and/or very particularly preferred meanings given above.

Particularly preferred starting materials for the process according to the invention are the compounds of the formula (II-g)

in which

• R¹ represents halogen, methyl, methoxy, trifluoromethyl or trifluoromethoxy,
• R⁴ represents phenyl which is mono- or disubstituted by radicals from the list W¹ or represents heterocyclyl which is mono- or disubstituted from the list W² or represents the grouping —Y—E,
• R⁵ represents hydrogen or alkoxy and
• Y, E, W¹ and W² have the general, preferred, particularly preferred and/or very particularly preferred meanings given above.

Very particular preference is given to starting materials of the formula (II-g) in which

• R¹ represents fluorine, chlorine, methyl, methoxy, trifluoromethyl or trifluoromethoxy,
• R⁴ represents phenyl which is mono- or disubstituted by radicals from the list W¹ or represents heterocyclyl which is mono- or disubstituted from the list W² or represents the grouping —Y—E,
• R⁵ represents hydrogen or C₁-C₆-alkoxy and
• Y, E, W¹ and W² have the general, preferred, particularly preferred and/or very particularly preferred meanings given above.

Especially preferred are starting materials of the formula (II-g) in which

• R¹ represents fluorine, chlorine, methyl, methoxy, trifluoromethyl or trifluoromethoxy,
• R⁴ represents phenyl which is mono- or disubstituted by radicals from the list W¹ or represents heterocyclyl which is mono- or disubstituted from the list W² or represents the grouping —Y—E,
• R⁵ represents hydrogen, methoxy or ethoxy and
• Y, E, W¹ and W² have the general, preferred, particularly preferred and/or very particularly preferred meanings given above.

In the definitions mentioned above, oxyalkylene and thioalkylene represent —O-alkyl- and —S-alkyl-, respectively, where the bond for example to Ar² is via the oxygen and sulfur atom, respectively, and further substituents may be attached to the alkyl radical, such as, for example, A in —X—A. Alkylenoxy and alkylenethio represent -alkyl-O— and -alkyl-S—, respectively, where the bond for example to Ar² is in each case via the alkyl radical and further substituents may be attached to the oxygen and sulfur atom, respectively, such as, for example, A in —X—A. Oxyalkylenoxy represents —O-alkyl-O—.

In the present description, heterocyclyl denotes a cyclic hydrocarbon in which one or more carbons are replaced by one or more heteroatoms. Preferred heteroatoms are O, S, N, P, in particular O, S and N.

Preferred, particularly preferred or very particularly preferred are compounds which carry the substituents mentioned under preferred, particularly preferred or very particularly preferred.

Saturated or unsaturated hydrocarbon radicals, such as alkyl or alkenyl, can in each case be straight-chain or branched as far as this is possible, including in combination with heteroatoms, such as, for example, in alkoxy.

Optionally substituted radicals can be mono- or polysubstituted, where in the case of polysubstitution the substituents can be identical or different. The plurality of radicals having the same indices, such as, for example, m radicals R⁵ for m >1, can be identical or different.

Halogen-substituted radicals, such as, for example, haloalkyl, are mono- or polyhalogenated. In the case of polyhalogenation, the halogen atoms can be identical or different. Halogen denotes fluorine, chlorine, bromine or iodine, in particular fluorine or chlorine.

However, the abovementioned general or preferred radical definitions or illustrations can also be combined with one another as desired, i.e. including combinations between the respective ranges and preferred ranges. They apply both to the end products and, correspondingly, to precursors and intermediates.

The aroylpyrrolidinones of the formula (II) required as starting materials for carrying out the process according to the invention are novel. They can be prepared by

• a) reacting lactams of the formula (III)

• • in which
  • Ar² is as defined above
  • with a compound of the formula (IV)

• • in which
  • Ar¹ is as defined above and
  • G represents chlorine, C₁-C₆-alkoxycarbonyl or —N(OCH₃)CH₃, in the presence of a base [for example lithium bis(trimethylsilyl)amide] and in the presence of a diluent (for example tetrahydrofuran) (cf. J. Org. Chem. 1998, 63, 1109; J. Org Chem. 1982, 47, 4165; Org. Prep. Proced. Int. 1995, 27, 510).

The formula (III) provides a general definition of the lactams required as starting materials for carrying out the process (a) according to the invention. In this formula, Ar² preferably, particularly preferably or very particularly preferably has those meanings which have already been mentioned in connection with the description of the starting materials of the formula (II) as being preferred, particularly preferred, etc., for these radicals.

Lactams of the formula (III) are known. They can be prepared, for example, by

• b) reacting pyrrolidinones of the formula (V)

• • in which
  • Ar² is as defined above
  • with di-tert-butyl dicarbonate in the presence of a base (for example dimethyl-aminopyridine) and, if appropriate, in the presence of a diluent (for example dimethylformamide) (cf. Tetrahedron Letters, 1998, 39, 2705-2706).

The formula (IV) provides a general definition of the compounds required as starting materials for carrying out the process (a) according to the invention. In this formula, Ar¹ preferably, particularly preferably or very particularly preferably has those meanings which have already been mentioned in connection with the description of the starting materials of the formula (II) as being preferred, particularly preferred, etc., for these radicals. G preferably represents chlorine, methoxycarbonyl, ethoxycarbonyl, i-propoxycarbonyl, t-butoxycarbonyl or —N(OCH₃)CH₃.

Compounds of the formula (IV) are known and/or can be prepared by known processes (cf. J. Prakt. Chem. 2000, 342, 340).

The formula (V) provides a general definition of the pyrrolidinones required as starting materials for carrying out the process (b) according to the invention. In this formula, Ar² preferably, particularly preferably or very particularly preferably has those meanings which have already been mentioned in connection with the description of the starting materials of the formula (II) as being preferred, particularly preferred, etc., for these radicals.

Pyrrolidinones of the formula (V) are known. They can be prepared, for example, by

• c) reacting ketocarboxylic acids of the formula (VI)

• • in which
  • Ar² is as defined above
  • with ammonia and hydrogen in the presence of a catalyst (for example Raney nickel) and, if appropriate, in the presence of a diluent (for example ethanol) under pressureor
• d) reacting hemi-aminals of the formula (VII)

• • in which
  • R⁹ represents alkyl or alkylcarbonyl
  • with aromatic compounds of the formula (VIII)H—Ar²  (VIII)
  • in which
  • Ar² is as defined above
  • with a protic acid (for example hydrofluoric acid) or with a Lewis acid and, if appropriate, in the presence of a diluent (for example dichloromethane)or
• e) reacting hemi-aminals of the formula (VII)

• • in which
  • R⁹ is as defined above
  • with metalloaromatic compounds of the formula (IX)M—Ar²  (IX)
  • in which
  • Ar² is as defined above and
  • M represents MgI, MgCl, MgBr, Li or ZnCl,
  • if appropriate in the presence of a diluent (for example diethyl ether, tetrahydrofuran, dioxane or anisol) (cf. Org. Prep. Proced. Int. 1993, 25, 255).

The formula (VI) provides a general definition of the ketocarboxylic acids required as starting materials for carrying out the process (c) according to the invention. In this formula, Ar² preferably, particularly preferably and very particularly preferably has those meanings which have already been mentioned in connection with the description of the starting materials of the formula (II) as being preferred, particularly preferred, etc., for these radicals.

Ketocarboxylic acids of the formula (VI) are known. They can be prepared, for example, by

• f) reacting aromatic compounds of the formula (VII)H—Ar²  (VIII)
  • in which
  • Ar² is as defined above
  • with succinic anhydride or 4-chloro-4-oxobutanoic acid in the presence of a Lewis acid (for example aluminum chloride) and, if appropriate, in the presence of a diluent (for example 1,2-dichloroethane) (cf. Org. Prep. Proced. Int. 1995, 27, 550)or
• g) for aromatic compounds which do not allow Friedel-Crafts acylation, alternatively using a corresponding metalloorganic derivative (for example a Grignard reagent) (cf. Syn. Commun. 1996, 26, 3897)or
• h) reacting α,β-unsaturated carbonyl compounds of the formula (X)

• • in which
  • Ar² is as defined above
  • in the presence of a reducing agent (for example Zn dust) and, if appropriate, in the presence of a diluent (for example glacial acetic acid) (cf. Chem. Pharm. Bull. 1988, 36, 2050).

The formula (VII) provides a general definition of the hemi-aminals required as starting materials for carrying out the processes (d) and (e) according to the invention. In this formula, R⁹ preferably represents C₁-C₆-alkyl or C₁-C₄-alkylcarbonyl. R⁹ particularly preferably represents C₁-C₄-alkyl, methylcarbonyl or t-butylcarbonyl. R⁹ very particularly preferably represents methyl, ethyl, i-propyl, t-butyl or methylcarbonyl.

Hemi-aminals of the formula (VII) are known and/or can be prepared by the known processes (cf. Tetrahedron 1975, 31, 1437; Heterocycles 1983, 20, 985).

The formula (VIII) provides a general definition of the aromatic compounds required as starting materials for carrying out the processes (d) and (f) according to the invention. In this formula, Ar² preferably, particularly preferably and very particularly preferably has those meanings which have already been mentioned in connection with the description of the starting materials of the formula (II) as being preferred, particularly preferred, etc., for these radicals.

Aromatic compounds of the formula (VIII) are known.

The formula (IX) provides a general definition of the metalloaromatic compounds required as starting materials for carrying out the process (e) according to the invention. In this formula, Ar² preferably, particularly preferably and very particularly preferably has those meanings which have already been mentioned in connection with the description of the starting materials of the formula (II) as being preferred, particularly preferred, etc., for these radicals. M preferably represents MgI, MgCl, MgBr, Li or ZnCl. M particularly preferably represents MgI, MgCl, MgBr or Li. M very particularly preferably represents MgCl, MgBr or Li.

Metalloaromatic compounds of the formula (IX) are known and/or can be prepared by known methods (for example lithiation or Grignard reaction) from the corresponding aromatic compounds or halogenated aromatic compounds.

The formula (X) provides a general definition of the carbonyl compounds required as starting materials for carrying out the process (h) according to the invention. In this formula, Ar² preferably, particularly preferably and very particularly preferably has those meanings which have already been mentioned in connection with the description of the starting materials of the formula (II) as being preferred, particularly preferred, etc., for these radicals.

Carbonyl compounds of the formula (X) are known. They can be prepared, for example, by

• i) reacting acetophenones of the formula (XI)

• • in which
  • Ar² is as defined above
  • with glyoxalic acid in the presence of a base (for example sodium hydroxide) and, if appropriate, in the presence of a diluent (for example water or ethanol) (cf. J. Med. Chem. 1996, 39, 4396).

The formula (XI) provides a general definition of the acetophenones required as starting materials for carrying out the process (i) according to the invention. In this formula, Ar² preferably, particularly preferably and very particularly preferably has those meanings which have already been mentioned in connection with the description of the starting materials of the formula (II) as being preferred, particularly preferred, etc., for these radicals.

Acetophenones of the formula (XI) are known.

The process according to the invention is carried out in the presence of an acid. Suitable acids for carrying out the process according to the invention are all customary protic acids or strong organic acids (such as, for example, sulfonic acids) or halocarboxylic acids which can be used for such reaction. Preference is given to using hydrochloric acid, sulfuric acid, hydrofluoric acid, phosphoric acid, p-toluenesulfonic acid, methanesulfonic acid, trifluoroacetic acid or trichloroacetic acid.

Particular preference is given to using hydrochloric acid, sulfuric acid p-toluenesulfonic acid or trifluoroacetic acid, very particularly preferably sulfuric acid. If appropriate, the acid used can be employed in a mixture with water. If appropriate, the process according to the invention can be carried out in the presence of a diluent. Suitable diluents for carrying out the process according to the invention are organic acids. Preference is given to using propionic acid, acetic acid or formic acid. Particular preference is given to using acetic acid.

When carrying out the process according to the invention, very particular preference is given to using any mixture of sulfuric acid (as acid) and acetic acid (as diluent) and, if appropriate, water. Particularly suitable is a mixture of concentrated sulfuric acid, water and acetic acid in a ratio of 1:1:2 (volume/volume/volume=v/v/v) or 1:1:3 (v/v/v). However, it is also possible to adjust and employ other mixing ratios.

When carrying out the process according to the invention, the reaction temperatures can be varied within a relatively wide range. In general, the process is carried out at temperatures between 20° C. and 200° C., preferably at temperatures between 60° C. and 150° C.

Expediently, the course of the reaction is monitored by thin-layer chromatography. Depending on the nature of the compound of the formula (II) employed, the reaction time is between 0.5 h and 6 h.

When carrying out the process according to the invention, in general an excess of acid (between 1 mol and 50 mol) is employed per mole of aroylpyrrolidinone of the formula (II). However, it is also possible to choose other ratios of the reaction components. Work-up is carried out by customary methods. In general, the reaction mixture is made alkaline with sodium hydroxide, the product is extracted and the organic phase is washed, dried and concentrated under reduced pressure. The crude product is then freed of any residues that may still be present using customary methods (for example chromatography or recrystallization).

Some of the 2,5-bisaryl-Δ¹-pyrrolines of the formula (I), which can be prepared by the process according to the invention are known. Also known is their use for controlling pests. They are particularly suitable for controlling insects, arachnids and nematodes encountered in agriculture, in forests, in the protection of stored products and materials and in the hygiene sector (see WO 00/21958, WO 99/59968, WO 99/59967 and WO 98/22438).

If the starting materials used are compounds of the formula (II-b), novel insecticidally active Δ¹-pyrrolines of the formula (I-b)

in which

• Ar², R¹, R² and R³ have the general, preferred, particularly preferred or very particularly preferred meanings given aboveare obtained.

If the starting materials used are compounds of the formula (II-c), novel insectidally active Δ¹-pyrrolines of the formula (I-c)

in which

• Ar², R¹, R² and R³ have the general, preferred, particularly preferred or very particularly preferred meanings given aboveare obtained.

If the starting materials used are compounds of the formula (II-d), novel insecticidally active Δ¹-pyrrolines of the formula (I-d)

in which

• Ar¹, R⁴, R⁵ and m have the general, preferred, particularly preferred or very particularly preferred meanings given aboveare obtained.

If the starting materials used are compounds of the formula (II-e), novel insecticidally active Δ¹-pyrrolines of the formula (I-e)

in which

• Ar¹, R⁴ and R⁵ have the general, preferred, particularly preferred or very particularly preferred meanings given aboveare obtained.

If the starting materials used are compounds of the formula (II-f), novel insecticidally active Δ¹-pyrrolines of the formula (I-f)

in which

• R¹ represents halogen, methyl, methoxy, trifluoromethyl or trifluoromethoxy,
• R² represents hydrogen or halogen,
• R⁴ represents phenyl which is mono- or disubstituted by radicals from the list W¹ or represents heterocyclyl which is mono- or disubstituted from the list W² or represents the grouping —Y—E,
• R⁵ represents hydrogen or alkoxy and
• Y, E, W¹ and W² have the general, preferred, particularly preferred and/or very particularly preferred meanings given aboveare obtained.

Preferably obtained are compounds of the formula (I-f) in which

• R¹ represents fluorine, chlorine, methyl, methoxy, trifluoromethyl or trifluoromethoxy,
• R² represents hydrogen, fluorine or chlorine,
• R⁴ represents phenyl which is mono- or disubstituted by radicals from the list W¹ or represents heterocyclyl which is mono- or disubstituted from the list W² or represents the grouping —Y—E,
• R⁵ represents hydrogen or C₁-C₆-alkoxy and
• Y, E, W¹ and W² have the general, preferred, particularly preferred and/or very particularly preferred meanings given above.

Particularly preferably obtained are compounds of the formula (I-f) in which

• R¹ represents fluorine, chlorine, methyl, methoxy, trifluoromethyl or trifluoromethoxy,
• R² represents hydrogen, fluorine or chlorine,
• R⁴ represents phenyl which is mono- or disubstituted by radicals from list W¹ or represents heterocyclyl which is mono- or disubstituted from the list W² or represents the grouping —Y—E,
• R⁵ represents hydrogen, methoxy or ethoxy and
• Y, E, W¹ and W² have the general, preferred, particularly preferred and/or very particularly preferred meanings given above.

If the starting materials used are compounds of the formula (II-g), novel insecticidally active Δ¹-pyrrolines of the formula (I-g)

in which

• R¹ represents halogen, methyl, methoxy, trifluoromethyl or trifluoromethoxy,
• R⁴ represents phenyl which is mono- or disubstituted by radicals from the list W¹ or represents heterocyclyl which is mono- or disubstituted from the list W² or represents the grouping —Y—E,
• R⁵ represents hydrogen or alkoxy and
• Y, E, W¹ and W² have the general, preferred, particularly preferred and/or very particularly preferred meanings given aboveare obtained.

Preferably obtained are compounds of the formula (I-g) in which

• R¹ represents fluorine, chlorine, methyl, methoxy, trifluoromethyl or trifluoromethoxy,
• R⁴ represents phenyl which is mono- or disubstituted by radicals from the list W¹ or represents heterocyclyl which is mono- or disubstituted from the list W² or represents the grouping —Y—E,
• R⁵ represents hydrogen or C₁-C₆-alkoxy and
• Y, E, W¹ and W² have the general, preferred, particularly preferred and/or very particularly preferred meanings given above.

Particularly preferably obtained are compounds of the formula (I-g) in which

• R¹ represents fluorine, chlorine, methyl, methoxy, trifluoromethyl or trifluoromethoxy,
• R⁴ represents phenyl which is mono- or disubstituted by radicals from the list W¹ or represents heterocyclyl which is mono- or disubstituted from the list W² or represents the grouping —Y—E,
• R⁵ represents hydrogen, methoxy or ethoxy and
• Y, E, W¹ and W² have the general, preferred, particularly preferred and/or very particularly preferred meanings given above.

Novel Δ¹-pyrrolines of the formulae mula (I-b), mula (I-c), mula (I-d), (I-e), (I-f) and (I-g) which can be obtained, for example, by the process according to the invention are also claimed according to the invention.

The practice of the process according to the invention is illustrated by the examples below.

PREPARATION EXAMPLES

Example 1

2.1 g (4 mmol) of tert-butyl 3-(2-bromobenzoyl)-2-oxo-5-[4-(trifluoromethoxy)phenyl]-1-pyrrolidinecarboxylate (II-1) are boiled at reflux in 15 ml of glacial acetic acid and 5 ml of concentrated sulfuric acid and 5 ml of water for 3.5 h. After cooling, the reaction mixture is made alkaline using dilute sodium hydroxide solution, the product is extracted with dichloromethane and the organic phase is concentrated under reduced pressure. The residue is chromatographed on silica gel (mobile phase: dichloromethane).

This gives 0.95 g (61.8% of theory) of 5-(2-bromophenyl)-2-[4-(trifluoro-methoxy)phenyl]-3,4-dihydro-2H-pyrrole as an oil.

HPLC: log P (pH 2.3)=3.61.

Analogously to example 1, it is possible to obtain the compounds listed in the table below.

No.	Structure	logP	m.p. (° C.)
2		3.90a)
3		5.11a)	56-58
4		3.09a)5.45b)	77-80
5		2.55a)5.23b)	58-60
6		5.70a)
7		4.83a)	42-44
8		5.69a)	68-70
9		2.41a)
10		1.63a)
11
12		3.77a)	80-82
13		5.18a)	78-80
14		2.94a)5.01b)	80
15		2.99a)
16		4.67a)5.94b)	53-54
17		3.45a)5.84b)	70-72
18		3.25a)6.10b)	110-112
19		6.19a)	64-66
20		3.05a)
21		2.74a)
22		2.09a)
23		3.06a)
24		2.33a)5.06b)
25		2.11a)5.01b)
26		3.36a)5.21b)
27		2.31a)
28		3.18a)4.62b)
29		3.55a)4.63b)
30		2.06a)4.79b)
31		1.41a)
32		1.12a)3.34b)	60-61
33		1.98a)4.05b)	57-59
34		1.63a)3.99b)	60-62
35			130-140
36		2.18a)
37		3.78a)3.95b)
38		3.52a)4.86b)
39		2.09a)4.51b)
40		1.97a)3.52b)
41		4.50b)
42		1.79a)3.50b)
43		2.22a)
44		2.68a)4.59b)
45		3.83a)4.75b)
46		4.66a)5.20b)
47		3.98a)4.88b)
48		1.73a)3.97b)
49		2.67a)3.86b)
50		2.39a)4.74b)
51		3.79a)4.36b)
52		3.01a)5.78b)
53		3.63a)
54		2.98a)4.67b)
55		2.19a)4.00b)
56		3.01a)3.89b)
57		3.31a)5.80b)
58		2.50a)4.03b)
59		2.88a)	112
60		2.90a)3.96b)
61		5.03a)5.33b)
62		3.36a)4.69b)
63		1.74a)3.74b)
64		2.73a)4.20b)
65		2.23a)4.31b)
66		2.02a)4.26b)
67		6.04b)
68		4.41b)
69		4.07b)
70		3.47a)5.33b)
71		2.82a)4.45b)
72		1.59a)4.06b)	115-16
73		4.13b)
74		1.96a)4.04b)
75		1.88a)3.06b)
76		1.16a)3.45b)
77		4.23a)6.03b)
78		3.84a)5.56b)
79		2.86a)5.95b)	85-87
80		2.55a)4.46b)
81		2.17a)4.07b)
82		2.60a)4.23b)
83		2.96a)4.22b)
84		2.14a)3.09b)
85		1.62a)3.88b)
86		1.66a)3.47b)
87		1.21a)3.32b)
88		3.77a)5.35b)
89		2.76a)4.36b)
90		1.43a)	84
91		1.64a)3.61b)
92		2.17a)	96
93		1.75a)
94		1.29a)3.70b)
95		2.00a)3.68b)
96		3.14a)
97		1.83a)
98		3.11a)
99		2.18a)
100		1.73a)4.14b)	68-70
101		3.51a)5.95b)	132-134
102		4.52a)5.56b)	55-57
103		3.26a)
104		0.59a)	110
105		4.87a)
106		0.91a)
107		3.26a)
108		3.41a)	70
109		3.61a)	74
110		2.14a)
111		4.55a)
112		4.57a)
113		3.98a)
114		5.05a)
115		5.46a)
116		2.94a)
117		4.57a)
118		5.05a)
119		4.17a)
120		4.63a)

Preparation of Starting Materials of the Formula (II)

Example (II-1)

At −50° C., 12 ml (11.6 mmol) of a 1 molar solution of lithium bis(trimethylsilyl)amide in tetrahydrofuran are added dropwise to a solution of 2.0 g (5.8 mmol) of tert-butyl 2-oxo-5-[4-(trifluoromethoxy)phenyl]-1-pyrrolidinecarboxylate (III-1) in 30 ml of tetrahydrofuran and 1.15 g (6.5 mmol) of hexamethylphosphoric triamide. After 10 min of stirring at −50° C., 1.4 g (6.4 mmol) of 2-bromobenzoyl chloride (dissolved in 5 ml of tetrahydrofuran) are then added, and the reaction mixture is allowed to warm to room temperature over a period of 16 h. The mixture is poured into water, acidifed with dilute hydrochloric acid and extracted with dichloromethane. The organic phase is separated off and concentrated under reduced pressure. The residue is triturated with pentane/ethyl acetate and filtered off with suction.

This gives 2.3 g (75.1% of theory) of 3-(2-bromobenzoyl)-2-oxo-5-[4-(trifluoro-methoxy)phenyl]-1-pyrrolidinecarboxylate.

m.p.: 113° C.

HPLC: log P (pH 7.5)=3.35.

In general, compounds of the formula (II) are directly reacted further, without purification.

Analogously to example (II-1), it is possible to obtain the compounds listed in the table below.

No.	Structure	logP	m.p. (° C.)
II-2		4.13a)	160-162
II-3		3.03b)
II-4		5.51b)	80-86
II-5		5.05b)
II-6		4.60b)	134-136

Preparation of Starting Materials of the Formula (III)

Example (III-1)

13.6 g (55 mmol) of 5-[4-(trifluoromethoxy)phenyl]-2-pyrrolidinone (V-1) in 60 ml of dimethylformamide are, with addition of 0.4 g of dimethylaminopyridine, stirred with 27.6 g (0.13 mol) of di-tert-butyl dicarbonate at 20° C. for 16 h. Most of the solvent is then removed, and the residue is partitioned between water and dichloromethane. The organic phase is again washed with water and concentrated under reduced pressure. The residue is triturated with pentane and filtered off with suction.

This gives 13.7 g (72.1% of theory) of tert-butyl 2-oxo-5-[4-(trifluoromethoxy)phenyl]-1-pyrrolidinecarboxylate.

m.p.: 120° C.

HPLC: log P (pH 2.3)=3.28.

Analogously to example (III-1), it is possible to obtain the compounds listed in the table below. Purification is either as described in the example or by recrystallization or by chromatography.

No.	Structure	logP	m.p. (° C.)
III-2		2.52a)	92-94
III-3		4.67a)	150-152
III-4		3.92a)	121
III-5		3.65a)	110
III-6		3.24a)3.25b)	110-112
III-7		2.43a)	113-115
III-8		2.43a)	64-65
III-9		3.83a)	96-97
III-10		3.54a)	99-100
III-11		3.29a)	124-127
III-12		2.67a)	120-122
III-13		2.93a)	134-136
III-14		3.30a)	119-120
III-15		2.84a)2.83b)	120
III-16		2.69a)	85-87
III-17		3.20a)	60-62
III-18		4.71a)	119-120
III-19		4.11a)	118-23
III-20		2.90a)	85-87
III-21		2.57a)	117
III-22		4.32a)	130
III-23		4.17a)	166
III-24		4.93a)	152
III-25		5.03a)	132
III-26		3.85a)
III-27		4.26a)	163-164
III-28		4.40a)

Preparation of Starting Materials of the Formula (V)

Example (V-1)

With 70 ml of liquid ammonia and 2 g of Raney nickel, 19.0 g (72 mmol) of 3-(4-trifluoromethoxybenzoyl)propionic acid in 170 ml of ethanol are, under a hydrogen pressure of 150 bar, heated at 150° C. for 3 h. After cooling, the catalyst is filtered off, the solvent is removed under reduced pressure and the residue is triturated with pentane.

This gives 14.4 g (81.7% of theory) of 5-[4-(trifluoromethoxy)phenyl]-2-pyrrolidinone of melting point 105-106° C.

HPLC: logP (pH 2.3)=2.00.

Example (V-2)

Hydrogen fluoride (2500 ml) is initially charged at 0° C. A solution of 5-ethoxy-2-pyrrolidinone (264 g, 2.04 mol) and 4-[(trifluoromethyl)thio]-1,1′-biphenyl (260 g, 1.02 mol) in dichloromethane (400 ml) is added dropwise. The reaction mixture is then stirred at room temperature, and the hydrogen fluoride is finally removed under reduced pressure. The residue is taken up in dichloromethane and washed with saturated aqueous sodium bicarbonate solution. The organic phase is dried over magnesium sulfate, filtered and concentrated. The crude products of two batches are combined and initially stirred with toluene. The crude product is then purified by silica gel chromatography (mobile phase: ethyl acetate/ethanol 7:3 v/v).

This gives off 5-{4′-[(trifluoromethyl)thio]-1,1′-biphenyl-4-yl}-2-pyrrolidinone “para” isomer: 173.2 g (25% of theory)

• • HPLC: log P (pH 2.3)=3.24 (99.5% purity) “ortho” isomer: 27.6 g (4% of theory)
  • HPLC: log P (pH 2.3)=3.15 (98.6% purity)

Example (V-3)

5-Ethoxy-2-pyrrolidinone (11.5 g, 0.1 mol) is initially charged at 0° C. in a mixture of glacial acetic acid (89 ml) and concentrated sulfuric acid (10 ml). 1-Tert-butyl-3-ethoxybenzene (19.61 g, 0.11 mol) is added, and the reaction mixture is then stirred at 0° C. for 2 h and at room temperature for 48 h. The reaction mixture is poured onto ice and repeatedly extracted with ethyl acetate. The combined organic phases are washed with aqueous saturated sodium bicarbonate solution, dried over magnesium sulfate, filtered and concentrated.

This gives 23.62 g (75% of theory) of 5-(4-tert-butyl-2-ethoxyphenyl)-2-pyrrolidinone.

HPLC: log P (pH 2.3)=2.84 (83% purity)

Analogously to one of examples (V-1) to (V-3), it is possible to obtain the compounds listed in the table below. Purification is either as described in the example or by recrystallization or by chromatography.

No.	Structure	logP	m.p. (° C.)
V-4		1.90a)	157-160
V-5		2.13a)	100-102
V-6		1.86a)	175-179
V-7		1.92a)	140-142
V-8		2.02a)	ca. 140
V-9		1.29a)	104-106
V-10		1.92a)	103-105
V-11		1.61a)	101-104
V-12		1.92a)	74-76
V-13		1.43a)	96
V-14		1.52a)	110-112
V-15		1.21a)	104
V-16		1.72a)	138-140
V-17		1.32a)	124-126
V-18		1.47a)	296
V-19		0.55a)	218
V-20		2.39a)	178
V-21		2.77a)	140
V-22		3.62a)	210
V-23		3.83a)	200
V-24		2.78a)	Decompositionfrom 187
V-25		1.59a)	161-163
V-26		2.69a)	68
V-27		2.96a)
V-28		2.76a)

The logP values given in the tables and preparation examples above are determined in accordance with EEC directive 79/831 Annex V.A8 by HPLC (High Performance Liquid Chromatography) on a reverse-phase column (C 18). Temperature: 43° C.

In the acidic range, the determination is carried out at pH 2.3 using the mobile phases 0.1% aqueous phosphoric acid and acetonitrile; linear gradient from 10% acetonitrile to 90% acetonitrile. (In the tables, the measurement values obtained are marked ^a).)

In the neutral range, the determination is carried out at pH 7.5 using the mobile phases 0.01 molar aqueous phosphate buffer solution and acetonitrile; linear gradient from 10% acetonitrile to 90% acetonitrile. (In the tables, the measurement values obtained are marked ^b).)

Calibration is carried out using unbranched alkan-2-ones (having 3 to 16 carbon atoms) with known logP values (determination of the logP values by the retention times using linear interpolation between two successive alkanones).

The lambda max values were determined in the maxima of the chromatographic signals using the UV spectra from 200 nm to 400 nm.

Claims

1. A process for preparing a 2,5-bisaryl-Δ1-pyrroline of the Formula (I)

2. A process as claimed in claim 1, wherein the aroylpyrrolidinone of the Formula (II) is

3. A process as claimed in claim 1, wherein the aroylpyrrolidinone of the Formula (II) is

4. A process as claimed in claim 1, wherein the aroylpyrrolidinone of the Formula (II) is

5. A process as claimed in claim 1, wherein the aroylpyrrolidinone is a compound of the Formula (II-a)

6. A process as claimed in claim 1, wherein the aroylpyrrolidinone is a compound of the Formula (II-a)

7. A process as claimed in claim 1, wherein the aroylpyrrolidinone is a compound of the Formula (II-a)

8. A process as claimed in claim 1, wherein the aroylpyrrolidinone is a compound of the Formula (II-b)

9. A process as claimed in claim 1, wherein the aroylpyrrolidinone is a compound of the Formula (II-c)

10. A process as claimed in claim 1, wherein the aroylpyrrolidinone is a compound of the Formula (II-d)

11. A process as claimed in claim 1, wherein the aroylpyrrolidinone is a compound of the Formula (II-e)

12. A process as claimed in claim 1, wherein the aroylpyrrolidinone is a compound of the Formula (II-f)

13. A process as claimed in claim 1, wherein the aroylpyrrolidinone is a compound of the Formula (II-g)

14. A process as claimed in claim 1, wherein the acid is a protic acid or a strong organic acid or a halocarboxylic acid.

15. A process as claimed in claim 1, wherein the acid is hydrochloric acid, sulfuric acid, hydrofluoric acid, phosphoric acid, p-toluenesulfonic acid, methanesulfonic acid, trifluoroacetic acid or trichloroacetic acid.

16. A process as claimed in claim 1, wherein the diluent is an organic acid.

17. A process as claimed in claim 1, wherein the diluent is propionic acid, acetic acid or formic acid.

18. A process as claimed in claim 1, wherein said acid and said diluent comprise a mixture of sulfuric acid, acetic acid and said mixture further comprises water.

19. A process as claimed in claim 1, wherein the reaction is carried out at temperatures between 20° C. and 200° C.