WO2003014107A1

WO2003014107A1 - Process for the preparation of heterocyclic pentalene derivatives

Info

Publication number: WO2003014107A1
Application number: PCT/EP2002/007680
Authority: WO
Inventors: Ilya E. Nifant'ev; Vladimir V. Bagrov
Original assignee: Basell Polyolefine Gmbh
Priority date: 2001-08-01
Filing date: 2002-07-10
Publication date: 2003-02-20
Also published as: EP1412347B1; JP2005501841A; ATE315559T1; EP1412347A1; DE60208683T2; US6930190B2; DE60208683D1; US20040192931A1

Abstract

A process for preparing heterocyclic pentalene derivative having formula (I): wherein w is a sulfur atom (S), an oxygen atom (O) or a NR or PR group, wherein R is an hydrocarbon group; R?1, R2, R3, and R4¿, equal to or different from each other, are hydrogen atoms or hydrocarbon groups; said process comprising the following steps: a) contacting a compound of formula (II) T is a OR, NR¿2?, CCI3, CF3, C1, Br, I, imidazolil or pirazolyl radical; with at least one molar equivalent of a vinyl compound of formula (III): wherein M is MgHal, Li, K, ZnHal, wherein Hal is chlorine, bromine or iodine; (II), (III) b) treating the compound of formula obtained in step a) with a Bronsted acid; c) treating the compound obtained in step b) with a reducing agent; and d) dehydrating the alcohol obtained in step c) in order to obtain the compound of formula (I).

Description

PROCESS FOR THE PREPARATION OF HETEROCYCLIC PENTALENE DERIVATIVES

The present invention relates to a new process for preparing heterocyclic pentalenes derivatives of formula:

wherein R¹, R², R³ and R⁴ represent hydrogen or hydrocarbon rests and W is an oxygen atom, a sulfur atom or a NR or PR group and R is an hydrocarbon rest.

Heterocyclic pentalenes are well known in the art for various uses. For example substituted thiophenes and b, d-ortho-fused thiophenes are used as reference materials in the analysis of sulphur-containing substances of fossil raw materials, such as mineral oils, coal, carbonaceous oils, shale oils and tar sands, as model systems for studying the desulphurisation of the aforementioned fossil raw materials, also on a technical scale, as oxidation inhibitors, for example in lubricants and as active substances in the fields involving biocides.

Recently they have been used for the preparation of metallocene complexes useful as catalysts for the polymerization of olefms. For example in J. Am. Chem. Soc. 1998, 120, 10786-10787

Ewen et al. describe metallocene compounds containing thiopentalene and azapentalene derivatives. Also PCT/EP00/12406 describes metallocene compounds containing thiopentalenes ligands. Catalyst based on these compounds produce polypropylene having a high degree of isotacticity. However the synthesis of these compounds involves several steps with low yields and, moreover, some derivatives are not accessible according to the routes proposed in these documents.

Therefore, a new process that permits to obtain these compounds in higher yields and with simple steps would be desirable.

The applicant has now found a new process that permits to overcome the above drawbacks and, moreover, to obtain a broader class of compounds.

An object of the present invention is a process for preparing heterocyclic pentalene derivatives having formula (I):

(I) wherein

W is a sulfur atom, an oxygen atom or a NR or PR group wherein R is a linear or branched saturated or unsaturated CrC₂₀-alkyl, C₃-C₂o~cycloalkyl, C₆-C₂₀-aryl, C₇-C o~alkylaryl or C₇-C o-arylalkyl radical, optionally containing heteroatoms belonging to groups 13-17 of the Periodic Table of the Elements; preferably the group NR is N-methyl or N-phenyl; and the group PR is P-methyl or P-phenyl; more preferably W is a sulfur atom; R¹, R², R³ and R⁴, equal to or different from each other, are hydrogen atoms or a linear or branched saturated or unsaturated C₁-C ₀-alkyl, C -C₂₀-cycloalkyl, C₆-C₂o-aryl, C₇-C₂₀-alkylaryl or C₇-C₂o~arylalkyl radical, optionally containing heteroatoms belonging to groups 13-17 of the Periodic Table of the Elements; or R¹ and R² and/or R³ and R⁴ can form a C -C₇ ring optionally containing O, S, N, P or Si atoms, said ring optionally bearing Cι-C₂₀ alkyl substituents or being optionally fused with a C₄-C₇ ring optionally containing O, S, N, P or Si atoms, such as a benzene or a cyclopentadiene ring; preferably R¹ is hydrogen, a Cι-C₂₀-alkyl or C₇-C o-arylalkyl radical; more preferably R¹ is a methyl, a phenyl or a Cι-C₁₀ alkyl substituted phenyl radical; preferably R² is hydrogen or a C₇-C₂o-arylaikyl radical; more preferably R² is a phenyl or a C o alkyl-substituted phenyl radical; preferably R³ is hydrogen or a C]-C₂o-alkyl radical; and preferably R⁴ is hydrogen, a C₁-C ₀-alkyl or C₇-C₂₀-arylalkyl radical; more preferably R⁴ is a methyl, or a phenyl radical; said process comprising the following steps: a) contacting a compound of formula (II):

(II) wherein R¹ and R² are defined as above and T is a OR, NR₂, OH, CC1₃, CF₃, Cl, Br, I, imidazolyl or pirazolyl radical; with at least one molar equivalent of a vinyl compound of formula (III):

(III) wherein R³ and R are defined as above and M is MgHal, Li, K, ZnHal, wherein Hal is chlorine, bromine or iodine; to form a compound of formula (IN):

(IN) b) treating the compound of formula (IN) with a Brønsted acid to form a compound of formula (N):

(V) c) treating the compound of formula (V) with a reducing agent to form the correspondent alcohol of formula (VI);

and d) dehydrating the alcohol of formula (VI). Νon limitative examples of compounds of formula (T) axe:

Compounds of formula (IT) used in step a) can be prepared with methods generally known in the art. For example when W is a sulfur atom these compounds can be prepared according to the process described in J. Chem. Soc. Perkin 1, 1976, vol. 22, 2355-2360.

Compounds of formula (HI) can be easily prepared starting from the correspondent vinyl bromide or they can be purchased as such.

Step a) is carried out at a temperature range of from -78 C to 100°C, preferably from -20°C to 20°C. Usually aprotic solvents are used, such as toluene, diethyl ether, hexane, tetrahydrofuran, dimethyl formamide, etc. The product obtained from step a) is purified by process known in the art such as filtration, crystallization, chromatography, distillation; otherwise it is used as such.

Preferably in the compound of formula (II) T is a NR₂ group; more preferably T is a N(Me)₂ or a N(Et)₂ radical. In the compound of formula (ILT) preferably the group M is MgBr or Li.

Examples of Brønsted acid used in step b) are methanesulphonic acid, sulfuric acid, phosphoric acid, polyphosphoric acid or P₂θ₅/methansulfuric acid. Preferably methanesulphonic acid or sulfuric acid are used. The reaction is preferably carried out in water or in an organic solvent such as dichloromethane, diethyl ether, tetrahydrofuran, dimethyl formamide, or in mixtures of water and organic solvents optionally in the present of a phase transfer agent. The reaction is carried out at a temperature range from 0°C to 100°C.

The amount of acid in step b) depends from the acid, usually a large excess of acid is used for example from 10 to 10000 equivalents or more.

The product obtained from step b) is purified by processes known in the art such as filtration, crystallization, chromatography, distillation; otherwise it is used as such.

Examples of reducing agents that can be used in step c) can be found in "Comprehensive

Organic Transformations" ed. 1989 NCH Publishers pages 527-552. For example LiAlH ,

A1H₃, ΝaBH or LiHAl(OtBu)₃ can be used. Preferably LiAlH is used.

The type of solvent used in step c) depends from the reducing agent used. In the case of

LiAlH₄, AIH₃, NaBH₄ or LiHAl(OtBu)₃ the reaction is carried out in an aprotic solvent such as toluene, diethyl ether, hexane, tetrahydrofuran, dimethyl formamide, at a temperature range of from -78 C to 100°C, preferably from 0°C to 80°C. The product obtained from step c) is purified by processes known in the art such as filtration, crystallization, chromatography, distillation; otherwise it is used as such.

Step d) is carried out by treating the alcohol of formula (VI) with a dehydrating agent.

Examples of dehydrating agent can be found in "Comprehensive Organic Transformations" ed. 1989 NCH Publishers pages 151-153. Example of dehydrating agent are p-toluenesulfonic acid, sulfuric acid, hydrochloric acid and iodine. Preferably p-toulensulfonic acid and iodine are used.

The amount of dehydrating agent depends from the dehydrating agent used. It can vary from one equivalent to a large excess such as 1000 equivalents and more. The type of solvent used in step d) depends from the dehydrating agent used. In the case of p- toulensulfonic acid the reaction is carried out in an aprotic solvent such as toluene, diethyl ether, hexane, tetrahydrofuran, dimethyl formamide, at a temperature range of from 0°C to

100°C, preferably from 20°C to 80°C. The product obtained from step d) is purified by processes known in the art such as filtration, crystallization, chromatography, distillation. A further method for purifying compounds obtained in step d) is treating the crude reaction product with at least one equivalent of an organolithium compound such as butylithium, methyllithium, tertbuthylithium and phenyllithium and filtering the obtained salt.

Steps a), b, c) and d) of the process of the present invention may be carried out in sequence without purification of the intermediate products.

Preferably steps c) and d) are carried out "one pot", i.e. without purification of the alcohol of formula (VI).

Compounds of formula (I) can be used as ligands for the synthesis of metallocene complexes, such as those described in WO 01/44318. These complexes are useful as catalyst components for polymerizing alpha-olefins. The syntheses of the metallocene compounds starting from the compounds of the present invention are described in the above mentioned application.

Generally, the compounds of formula (I) can be treated with a base and then contacted with a compound of formula YL'Cp wherein Y is halogen, preferably chlorine, L' is a suitable bridge and Cp is a substituted or unsubstituted cyclopentadienyl radical. The obtained bridged ligand is then treated with two equivalents of a base and contacted with the compound of formula ML"₄ wherein M is titanium, zirconium or hafnium and L is generally halogen, preferably chlorine. For unbridged metallocene compounds the compound of formula (I) is treated with a base and then the correspondent anion is contacted with a compound of formula

ML"₄.

The following examples are given for illustrative purposes and are not intended to limit the scope and spirit of the invention.

EXAMPLES

General procedures.

Operations moisture sensitive were performed under nitrogen by using conventional Schlenk- line techniques. Solvents were purified by degassing with N₂ and passing over activated (8 hours, N purge, 300 °C) Al₂O₃, and stored under nitrogen. «-BuLi (Aldrich) was used as received. Example 1 Synthesis of 2,3-diphenyl-5-methyI-6 j^r-cyclopenta[£lthiophene

Preparation of the compound of formula (II) Synthesis of 2,3-Diphenyl-thienylcarbonyc acid

30.8g (O.lmol) of 2,3-diphenyl-5-carbetoxythiophene (prepared analogously to 2-methyl-3- phenyl-5-carbetoxythiophene with 70-80% yield from dezoxybenzoin) was treated with solution of 20g NaOH in 50ml water+50ml ethanol. Resulting mixture was refluxed in 3h and then was treated with 100 ml water. Aqueous phase was collected, added with HC1 aq. up to pH=3. White solid was isolated by filtration, washed with 100ml water and dried. Yield

100%.

1H NMR (Dimethylsulfoxide (DMSO)-d₆): 7.76 (s, 1H), 7.40-7.20 (m, 10H), 3.5 (br.s., water

+ acidic proton)

Synthesis of 2,3-Diphenyl-thienylcarbonyc acid dimethylamide

lOg (36mmol) of acid, 5.5ml SOCl₂ (75mmol), 0.1ml dimethylformamide (DMF) and 50 ml of benzene were placed into the bulb and refluxed in 2h. Then the mixture was evaporated. Resulting oil was dissolved in 10ml of tetrahydrofuran (THF) and this solution was added dropwise to 30ml 33% aqueous Me₂NH at 0°C. The mixture was stirred in 30min. The precipitate was isolated, washed with water and dried. Yield lOg (92%). 1H NMR (CDC1₃): 7.45 (s, 1H), 7.40-7.20 (m, 10H), 3.40-3.20 (br.s., 6H) Step a) l-(4,5-Diphenyl-2-thienyl)-2-methyl-2-propen-l-on

10g (33mmol) of 2,3-Diphenyl-thienylcarbonic acid dimethylamide was dissolved in 15ml THF and the resulting solution was added dropwise to solution of propenylmagnesium bromide prepared from 0.78 g Mg (33mmol) and 4g 2-bromopropene (33mmol) in 50ml THF at -40°C. The mixture warmed to r.t. and was stirred in 4h. The resulting solution was poured into 100ml of 5% aqueous HC1. The organic layer was collected, washed with water, dried over MgSO₄ and evaporated to give yellow-reddish oil. Yield 9.5g (100%). The product is contaminated with 5-10% of starting amide (by NMR) and can be used without further purification. Step b) 5-Methyl-2,3-diphenyl-4,5-dihydro-6H-cyclopenta[b]thiophen-6-on

Solution from previous experiment was poured into 80 ml methanesulphonic acid (can be replaced by H₂SO₄) at 65°C. After 30 min of stirring at reflux the resulting mixture was poured into 400ml water/300ml dichlorometane mixture. The organic phase was collected, washed with aq. NaHCO₃ up to neutral reaction and dried over MgSO₄. The resulting solution was evaporated to give 8.8g viscous oil. This substance either have to be purified by chromatography on silica gel with benzene as an eluent (R_f of the product is ~ 0.15) or can be used as is.

^!H NMR (CDC1₃): 7.40-7.20 (m, 10H), 3.20 (dd, 1H), 3.06 (quintet of doublets, 1H), 2.67

(dd, 1H), 1.44 (d, 3H)

Steps c) and d) 5-Methyl-2,3-diphenyl-4H-cyclopenta[b]thiophene

Solution of 7g (0.023 mol) 5-methyl-2,3-diphenyl-4,5-dihydro-6H-cyclopenta[ό]thiophen-6- on in 200ml ether was treated with 0.24g (0.0063mol) LiAlH in 100ml ether. The mixture was stirred in 30 min and then was poured in 300 ml of 10% NH C1. The organic phase was collected, dried over MgSO and evaporated. Resulting alcohol (6.7g, 95%) was dissolved in 350ml benzene. To this solution 0.25g p-toluenesulphonic acid and a few crystals of 2,6- di(tert-butyl)phenol were added. The resulting mixture was refluxed in 10 min, then was cooled to r.t, washed with saturated aq. NaHCO₃ and water. The solution so-obtained was dried over MgSO₄ and evaporated. The residue was recrystallized from hexane to give 4.2g (67% from ketone) of the product as yellowish crystalline solid.

1H NMR (C₆D₆): 7.45 (d, 2H), 7.31 (d, 2H), 7.15-6.90 (m, 6H), 6.20 (quintet, 1H); 2.73 (br.s, 2H); 1.80 (s, 3H) Example 2 Synthesis of 2-methyl-3,5-diphenyl-6iy-cyclopenta[Mthiophene

Preparation of the compound of formula (II) Synthesis of 3-chloro-2-phenyl-2-butenal

0.375 mol (35 mL) of POCl₃ was added at 0°C to a 0.45 mol (35 mL) of DMF. At the end of the addition, the mixture was allowed to warm up to room temperature and stirred for 30 min. Then it was cooled again to 0°C and carefully treated with 0.15 mol (20.1 g) of phenylacetone. The resulting reaction mixture was stirred at the same temperature for 1 h and then at 60-70°C in additional 4 hours (the reaction was monitored by NMR). The resulting viscous solution was poured into a mixture of ice and aqueous sodium acetate (150g). Product was extracted with CH₂C1₂ (3 x 50 mL). The organic phase was separated, washed with water until neutral pH, dried over MgSO and evaporated to dryness. The residue represents chloroaldehyde as a mixture of two forms (ratio of forms depends on the duration of chlorocarbonylation). It was used without further purification. Yield 19.2 (71%).

1H-NMR (CDC1₃): 10.47(s) and 10.15(s) (1H, CHO); 7.40-7.00 (group of multiplets, 5H, aromatic CH); 2.79(s) and 2.32(s) (3H, CH₃).

Note: do not use distillation to purify the product!

Synthesis of 5-methyl-4-phenyl-2-thiophene-ethylcarboxylate

Ethyl-2-mercaptoacetate (45.8 mmol, 5.0 mL) was added at 0°C to a solution of sodium ethoxide (46 mmol, 3.13 g) in 50 mL of ethanol and the resulting mixture was stirred at the same temperature for 30 min. Then 3-chloro-2-phenyl-2-butenal (45.8 mmol, 8.3 g) was added and stirring was continued overnight. The resulting product was refluxed for 2 h, cooled to room temperature and diluted in 100 mL of water. The organic layer was collected and the water layer was extracted with CH₂C1₂ (3 x 50 mL). The combined organic layers were dried over MgSO₄, evaporated to dryness and the residue was used in the next step without further purification. Synthesis of 5-methyl-4-phenyI-2-thiophenecarboxyIic acid

The 5-methyl-4-phenyl-2-thiophene-ethylcarboxylate coming from the previous step was added to a 30% solution of sodium hydroxide in 100 mL of ethanol and the resulting mixture was refluxed for 2 h. Then it was diluted in water and extracted with 50 mL of benzene. The water phase was isolated, acidified and the mixture was filtered. The precipitate was dried under P₂O₅. Yield 9.5 g (95% towards 3-chloro-2-phenyl-2-butenal).

1H-NMR (CDCI₃): 12.00-10.00 (br.s, 1H, COOH); 7.87 (s, 1H, thiopheneCH); 7.50-7.35 (m,

5H, phenylCH); 2.58 (s, 3H, CH₃).

Synthesis of 2-Methyl-3-phenyl-thienylcarbonyc dimethylamide

21.8g (O.lmol) of acid, 10.9ml SOCl₂ (0.15mmol), 0.5ml DMF and 150 ml of dichloromefhane were placed into the bulb and refluxed in 2h. Then the mixture was evaporated. Resulting oil was dissolved in 20ml THF and this solution was added dropwise to 50ml 33% aqueous Me₂NH at 0°C. The mixture was stirred in 30min. The resulting emulsion was poured into 500ml of water. Product was extracted with 2x50ml dichloromethane. Solution was washed with water, dried over magnesium sulfate and evaporated to give brown viscous liquid that tends to crystallize. Yield 28g (81%). 1H NMR (CDCI₃): 7.45 (s, 1H), 7.40-7.20 (m, 10H), 3.40-3.20 (br.s., 6H) Step a) l-(5-Methyl-4-phenyl-2-thienyl)-2-phenyl-2-propen-l-on

23.3g (lOOmmol) of 2-methyl-3-phenyl-thienylcarbonic acid dimethylamide was mixed with 100ml ether and the resulting suspension was added in some portions at 0°C to solution of 1- stiryllitium prepared from 62ml 1.6M BuLi in hexane (lOOmmol) and 27g 1-bromostyrene (150mmol) in 200ml ether. The mixture warmed to r.t. and was stirred in lh. The resulting solution was poured into 500ml of 5% aqueous HC1. The organic phase was collected, separated from insoluble impurities (these impurities presumably are due to the use of Li- derivative instead of Mg derivative in the previous case), washed with water, dried over MgSO₄ and evaporated to give yellow oil. Yield of crude product 15g (52%). The product can contaminated with 5-10% of starting amide (by NMR) and can be used without further purification.

1H NMR (CDCI₃): 7.61 (s, 1H), 7.55-7.35 (m, 10H), 6.03 (s, 1H), 5.82(s, 1H), 2.59 (s., 3H) Step b) 2-Methyl-3,5-diphenyl-4,5-dihydro-6H-cyclopenta[b]thiophen-6-on

Vinyl-ketone obtained in previous experiment was dissolved in 20ml of dichloromethane and resulting was poured into 50 ml methanesulphonic acid heated to 65°C. After 30 min of stirring at reflux the resulting mixture was poured into the mixture 0.31 water/ice/200ml dichlorometane. The organic phase was collected, washed with water, then with aq. NaHCO₃ up to neutral reaction and dried over MgSO₄. The resulting solution was evaporated to give

14g of viscous oil. This oil crystallizes on standing. This substance can be used for further steps (reduction by LiAlH₄ followed by dehydration without special purification.

1H NMR (CDC1₃): 7.55-7.20 (m, 10H), 4.15 (dd, 1H); 3.50 (dd, 1H); 3.07 (dd, 1H), 2.61 (s.,

3H)

Steps c) and d) 2-Methyl-3,5-diphenyl-4H-cyclopenta[b]thiophene

LiAlrL

Solution of 14g (47mmol) 2-Methyl-3,5-diphenyl-4,5-dihydro-6H-cyclopenta[b]thiophen-6- on in 150ml ether was treated with 0.63g (16mmol) LiAlH₄ in 100ml ether. The mixture was stirred in 30 min and then was poured in 300 ml of 10% NH₄C1. The organic phase was collected, dried over MgSO₄ and evaporated. Resulting alcohol (13.4g, 95%) was poured into solution lg p-toluenesulphonic acid in 11 toluene at 65 °C. The resulting mixture was stirred in 20 min at 80°C, then it was cooled to r.t, washed with saturated aq. NaHCO₃ and water. The solution so-obtained was dried over MgSO₄ and evaporated. The residue was isolated by chromatography on silica-gel (hexane/CH₂Cl₂ 3/1) to give 6.5g (53% from ketone) of yellowish crystalline solid. This solid consists of two isomers of position of double bond. 1H NMR (CDCI3): 7.60-7.20 (m, 10H), 7.21(m) and 7.14(m) (1H), 3.83 (br.s) and 3.68 (br.s) 2H); 2.60 (s, 3H) Example 3 Synthesis of 2,3,5-triphenyl-6H-cyclopenta[Z>]thiophene

Preparation of the compound of formula (II)

2,3-diphenyl-thienylcarbonic acid dimethylamide was prepared in analogous manner to 2- Methyl-3-phenyl-thienylcarbonyc dimethylamide with the exception that the starting compound was dibenzyl ketone instead of phenylacetone. Step a) l-(4,5-DiphenyI-2-thienyl)-2-phenyl-2-propen-l-on

30.7g (lOOmmol) of 2,3-diphenyl-thienylcarbonic acid dimethylamide was mixed with 100ml ether and the resulting suspension was added in some portions at 0°C to solution of 1- stiryllitium prepared from 62ml 1.6M BuLi in hexane (lOOmmol) and 27g 1-bromostyrene (150mmol) in 200ml ether. The mixture warmed to room temperature (r.t.) and was stirred for lh. The resulting solution was poured into 500ml of 5% aqueous HC1. The organic phase was collected, separated from insoluble impurities, washed with water, dried over MgSO₄ and evaporated to give 20.9g (57%) of crystalline solid. The product can be contaminated with 5- 10% of starting amide (by NMR) and can be used without further purification. 1H NMR (CDC1₃): 7.82 (s, 1H), 7.70-7.30 (m, 15H), 6.16 (s, 1H), 5.96(s, 1H) Note: technical- grade 1-bromo-styrene is available only. It was distilled before reaction and was taken in 50% excess. Step b) 2,3,5-triphenyl-4,5-dihydro-6H-cycIopenta[b]thiophen-6-on

Vinyl-ketone obtained in previous experiment was dissolved in 20ml of dichloromethane and resulting was poured into 50 ml methanesulphonic acid heated to 65°C. After 30 min of stirring at reflux the resulting mixture was poured into the mixture 0.31 water/ice/200ml dichlorometane. The organic phase was collected, washed with water, then with aq. NaHCO₃ up to neutral reaction and dried over MgSO₄. The resulting solution was evaporated to give 20g of crystalline product. This substance can be used for further steps (reduction by LiAlH₄ followed by dehydration) without special purification.

'H NMR CCDCls): 7.55-7.20 (m, 15H), 4.25 (dd, 1H); 3.61 (dd, 1H); 3.20 (dd, 1H) Steps c) and d) 2,3,5-Triphenyl-4H-cyclopenta[b]thiophene

ution of 3.7g (lOmmol) 2,3,5-triphenyl-4,5-dihydro-6H-cyclopenta[b]thiophen-6-on in 20ml ether was treated with 130mg (16mmol) LiAlH₄ in 10ml ether. The mixture was stirred in 30 min and then was poured in 50 ml of 10% NH₄C1. The organic phase was collected, dried over MgSO₄ and evaporated. Resulting alcohol was poured into solution of 300mg p- toluenesulphonic acid in 300ml toluene at 65°C. The resulting mixture was refluxed in 20 min, then it was cooled to r.t., washed with saturated aq. NaHCO₃ and water. The solution so- obtained was dried over MgSO₄ and evaporated. The residue was isolated by chromatography on silica-gel (hexane/CH₂Cl₂ 3/1) to give 2.1g (60% from ketone) of yellowish crystalline solid.

^!HNMR (CDC1₃): 7.60 (m, 2H), 7.45-7.25(m, 14H); 3.72 (d, 2H) Example 3 Synthesis of 2,5-dimethyl-3-(4-chloro-phenyl)-61/-cyclopentar61thiophene

Preparation of the compound of formula (II) Synthesis of (4-chloro-phenyl)-acetone

34g (0.224mol) (4-chloro-phenyl)benznitryl and 33ml (0.337mol) ethylacetate was added to the hot solution of 24g (0.3mol) sodium isopropilate in 150ml isopropanol. Reaction mixture was stirred at reflux in 3 hours then it was cooled to r.t., treated with 20g (0.3mol) acetic acid and finally diluted with 500ml water. Organic precipitate was extracted with 100ml dichloromethane. Resulting solution was evaporated to give yellowish solid of p-Cl- phenylacetone that was used without purification.

1H-NMR (CDC1₃): 7.44 (AA'BB' component, 2H); 7.36 (AA'BB' component, 2H); 4.68 (s, lH); 2.31 (s, 3H). p-Cl-phenylacetone prepared in previous experiment was added in small portions to 50ml of concentrated sulfuric acid at 0-5°C then the mixture was heated at stirring to 100°C in lOmin.

Then the reaction mixture was cooled to 0°C, was treated quickly with 250ml water and was stirred at 100°C in 3 hours. The resulting mixture was cooled to r.t., the organic layer was separated and distilled at 108-110/lOtorr to give 24.5g (65% from p-Cl-phenylacetone).

1H-NMR (CDCI3): 7.34 (AA'BB' component, 2H); 7.16 (AA'BB' component, 2H); 3.71 (s,

2H); 2.20 (s, 3H).

Synthesis of 5-methyl-4-(4-Cl-pheny)l-2-thiophenecarboxylic acid

17.5ml (0.19 mol) of POCl₃ was added at 0°C to a 32ml (0.44mol) of DMF. At the end of the addition, the mixture was allowed to warm up to room temperature and stirred for 30 min. Then it was cooled again to 0°C and carefully treated with 24.5g (0.145 mol) of p-Cl- phenylacetone. The resulting reaction mixture was stirred at the same temperature for 1 h and then at 60-70°C in additional 4 hours. The resulting viscous solution was poured into a mixture of ice and aqueous sodium acetate (150g). Product was extracted with CH C1₂ (3 x 50 mL). The organic phase was separated, washed with water until neutral pH, dried over MgSO₄ and evaporated to dryness. The residue represents 21.5 g (68%) of crude chloroaldehyde that was used as is.

Ethyl-2-mercaptoacetate (12g, O.lmol) was added at 0°C to a solution of sodium ethoxide (6.8g, O.lmol) in 150 mL of ethanol and the resulting mixture was stirred at the same temperature for 30 min. Then chloroaldehyde from the previous experiment (21.5g, O.lmol) was added and stirring was continued overnight. The resulting product was refluxed for 2 h, cooled to room temperature and then was treated with solution of 12g (0.3mol) NaOH in 20ml water. The resulting mixture was refluxed in 1 hour, then it was cooled to r.t. and finally was poured into 500ml of water. The resulting mixture was neutralized by aqueous HC1, the precipitate was isolated, washed twice with 200ml water and dried. Yield 15.3g (60%). 1H-NMR (DMSO): 7.52 (s, 1H, thiopheneCH); 7.47 (m, 4H, phenylCH); 2.46 (s, 3H, CH₃). Synthesis of 2-Methyl-3-(4-chloro-phenyl)-thienylcarbonyc dimethylamide

15.3g (O.Oόmol) of acid, 7.1ml SOCl₂ (O.lmmol), 0.1ml DMF and 100 ml of dichloromethane were placed into the bulb and refluxed in 30min. Then the mixture was evaporated. Resulting oil was dissolved in 20ml THF and this solution was added dropwise to 50ml 33% aqueous

Me NH at 0°C. The mixture was stirred in 30min. The resulting emulsion was poured into

500ml of water. Product was extracted with 2x50ml dichloromethane. Solution was washed with water, dried over magnesium sulfate and evaporated to give brown viscous liquid. Yield

14.4g (86%).

1H-NMR (CDC1₃): 7.45-7.30 (m, 5H); 3.25 (br.s, 6H); 2.50 (s, 3H).

Step a) 1 - [5-Methyl-4-(4-chloro-phenyl)-2-thienyl] -2-methyl-2-propen-l -on

7.2g (26mmol) of 2-methyl-3-(p-Cl-phenyl)-thienylcarbonic acid dimethylamide was dissolved in 15ml THF and the resulting solution was added dropwise to solution of 2- propenylmagnesium bromide prepared from lg Mg (42mmol) and 3.7g 2-bromopropene (31mmol) in 20ml THF at 0°C. The mixture warmed to r.t. and was stirred in 4h. The resulting solution was poured into 100ml of 5% aqueous HC1. The organic layer was collected, washed with water, dried over MgSO and evaporated to give quantitative amount yellow-reddish oil that was used without further purification.

1H NMR (CDCI₃): 7.56 (s, 1H); 7.39 (AA'BB' component, 2H); 7.29 (AA'BB' component, 2H); 5.79 (m, 1H), 5.74(m, 1H), 2.51 (s., 3H); 2.04 (m, 3H)

Ste b) 2,5-Dimethyl-3-(4-chloro-phenyI)-4,5-dihydro-6H-cyclopenta[b]thiophen-

6-on

Ninyl-ketone obtained in previous experiment was dissolved in 10ml of dichloromethane and resulting solution was poured into 25 ml methanesulphonic acid heated to 65°C. After 20 min of stirring at reflux the resulting mixture was poured into the mixture 0.21 water/ice/50ml dichlorometane. The organic phase was collected, washed with water, then with aq. NaHCO₃ up to neutral reaction and dried over MgSO₄. The resulting solution was evaporated and was purified by chromatography (hexane/ether 3/1) to give 2.2g (31%) of viscous oil. 1H NMR (CDC1₃): 7.41 (AA'BB' component, 2H); 7.23 (AA'BB' component, 2H); 3.13 (dd, 1H), 2.94 (quintet of doublets, 1H); 2.50 (s, 3H); 2.49 (dd, 1H), 1.31 (d, 3H) Steps c) and d) Synthesis of 2,5-dimethyl-3-(4-chloro-phenyl)-6H- cyclopenta [b] thiophene

ution of 2.2g (8mmol) 2,5-dimethyl-3-(4-chloro-phenyl)-4,5-dihydro-6H- cyclopenta[b]thiophen-6-on in 20ml ether was treated with O.lg (2.6mmol) LiAlH₄ in 20ml ether. The mixture was stirred in 30 min and then was poured in 30 ml of 10%> NH C1. The organic phase was collected, dried over MgSO and evaporated. Resulting alcohol was dissolved in 150ml benzene. To this solution O.lg p-toluenesulphonic acid. The resulting mixture was refluxed in 10 min, then was cooled to r.t., washed with saturated aq. NaHCO₃ and water. The solution so-obtained was dried over MgSO and evaporated to give 1.4g (67% from ketone) of the solid product.

1H NMR (CD₂C1₂): 7.37 (AA'BB' component, 2H); 7.32 (AA'BB' component, 2H); 6.38 (quintet, 1H); 3.06 (br.s., 2H); 2.43 (s, 3H); 2.10 (br.s, 3H).

Example 4 one pot Synthesis of 2,5-dimethyl-3-(4-chloro-phenyl)-6H- cyclopentafblthiophene lithium salt

15.3g (O.Oόmol) of acid, 7.1ml SOCl₂ (O.lmmol), 0.1ml DMF and 100 ml of dichloromethane were placed into the bulb and refluxed in 30min. Then the mixture was evaporated. Resulting oil was dissolved in 20ml THF and this solution was added dropwise to 50ml 33%₀ aqueous Me₂NH at 0°C. The mixture was stirred in 30min. The resulting emulsion was poured into 500ml of water. Product was extracted with 2x50ml dichloromethane. Solution was washed with water, dried over magnesium sulfate and evaporated to give brown viscous liquid. Viscous liquid so-obtained was dissolved in 15ml THF and the resulting solution was added dropwise to solution of 2-propenylmagnesium bromide prepared from 2g Mg (42mmoι) and 7.4g 2-bromopropene (62mmol) in 40ml THF at 0°C. The mixture warmed to r.t. and was stirred in 4h. The resulting solution was poured into 200ml of 5% aqueous HC1. The organic layer was collected, washed with water, dried over MgSO₄ and evaporated to give yellow- reddish oil of vinil-ketone.

Vinyl-ketone obtained in previous experiment was dissolved in 20ml of dichloromethane and resulting solution was poured into 50 ml methanesulphonic acid heated to 65°C. After 20 min of stirring at reflux the resulting mixture was poured into the mixture 0.41 water/ice/lOOml dichlorometane. The organic phase was collected, washed with water, then with aq. NaHCO₃ up to neutral reaction and dried over MgSO₄. The resulting solution was evaporated, then was dissolved in 50ml ether was treated with 675mg (15mmol) LiAlH₄ in 50ml ether. The mixture was stirred in 30 min and then was poured in 30 ml of 10% NH₄C1. The organic phase was collected, dried over MgSO₄ and evaporated. Resulting alcohol was dissolved in 300ml toluene. To this solution 0.2g p-toluenesulphonic acid was added. The resulting mixture was heated under stirring at 80°C in 10 min, then was cooled to r.t., washed with saturated aq. NaHCO₃ and water. The solution so-obtained was dried over MgSO₄ and evaporated to give 10.4g of crude ligand.

This crude product was dissolved in the mixture of 30ml ether and 100ml hexane and then was treated with 38ml of 1.6M BuLi in hexane (60mmol). The precipitate was isolated, washed with hexane and dried. Yield 7.5g.

Claims

1. A process for preparing heterocyclic pentalene derivatives having formula (I):

(I) wherein

W is a sulfur atom, an oxygen atom or a NR or PR group wherein R is selected from the group consisting of a linear or branched saturated or unsaturated Cι-C₂₀-alkyl, C₃-C₂₀-cycloalkyl, C₆-C₂o-aryl, C -C₂₀-alkylaryl and C -C o~arylalkyl radical, optionally containing heteroatoms belonging to groups 13-17 of the Periodic Table of the Elements; R¹, R², R³ and R⁴, equal to or different from each other, are hydrogen atoms or a linear or branched saturated or unsaturated Cι-C₂o-alkyl, C₃-C ₀-cycloalkyl, C₆-C₂o-aryl, C₇-C₂o-alkylaryl or C -C₂o-arylalkyl radical, optionally containing heteroatoms belonging to groups 13-17 of the Periodic Table of the Elements; or R¹ and R² and/or R³ and R⁴ can form a C₄-C₇ ring optionally containing O, S, N, P or Si atoms, said ring optionally bearing Cι-C₂₀ alkyl substituents or being optionally fused with a C -C₇ ring optionally containing O, S, N, P or Si atoms; said process comprising the following steps: a) contacting a compound of formula (II) :

(HI) wherein R³ and R⁴ are defined as aabboovvee and M is MgHal, Li, K, ZnHal, wherein Hal is chlorine, bromine or iodine; to form a compound of formula (IV)

(IN) b) treating the compound of formula (IV) with a Brønsted acid to form a compound of formula (V):

(N) c) treating the compound of formula (N) with a reducing agent to form the correspondent alcohol of formula (VI);

and d) dehydrating the alcohol of formula (VI).

2. The process according to claim 1 wherein in the compound of formula (I) the group ΝR is Ν-methyl or Ν-phenyl; the group PR is P-methyl or P-phenyl; R¹ is hydrogen, a Cι-C₂₀-alkyl or C₇-C₂₀-arylalkyl radical; R² is hydrogen or a C₇-C₂₀-arylalkyl radical; R³ is hydrogen or a CrC₂o-alkyl radical and R⁴ is hydrogen, a C₁-C₂₀-alkyl or C -C₂₀-arylalkyl radical.

3. The process according to claims 1 or 2 wherein in the compound of formula (I) W is a sulfur atom; R¹ is a methyl, a phenyl or a -Cio alkyl substituted phenyl radical; R² is a phenyl or a d- o alkyl-substituted phenyl radical and R is a methyl, or a phenyl radical.

4. The process according to anyone of claims 1 to 3 wherein in the compound of formula (II) T is NR group and in the compound of formula (III) the group M is MgBr or Li.

5. The process according to anyone of claims 1 to 4 wherein the Brønsted acid used in step b) are methanesulphonic acid, sulfuric acid, phosphoric acid, polyphosphoric acid or P θ₅/methansulfuric acid.

6. The process according to anyone of claims 1 to 5 wherein the reducing agent used in step c) is LiAlH₄, A1H₃, NaBH₄ or LiHAl(OtBu)₃.

7. The process according to anyone of claims 1 to 6 wherein the dehydrating agent used in step d) is p-toluenesulfonic acid, sulfuric acid, hydrochloric acid or iodine.

8. The process according to anyone of claims 1 to 7 wherein the compound obtained in step d) is purified by treating the crude reaction product with at least one equivalent of an organolithium compound and filtering the obtained salt.

9. The process according to anyone of claims 1 to 8 wherein steps a), b, c) and d) are carried out in sequence without purification of the intermediate products.

10. The process according to anyone of claims 1 to 8 wherein steps c) and d) are carried out without purification of the alcohol of formula (VI).