EP4178950A1 - Réactifs pour polyfluoroalkylthiolation de composés organiques et procédé de production associé - Google Patents

Réactifs pour polyfluoroalkylthiolation de composés organiques et procédé de production associé

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Publication number
EP4178950A1
EP4178950A1 EP21737060.0A EP21737060A EP4178950A1 EP 4178950 A1 EP4178950 A1 EP 4178950A1 EP 21737060 A EP21737060 A EP 21737060A EP 4178950 A1 EP4178950 A1 EP 4178950A1
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EP
European Patent Office
Prior art keywords
mmol
thio
nmr
compound
mhz
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EP21737060.0A
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German (de)
English (en)
Inventor
Jordi MESTRE
Omar BOUTUREIRA
Sergio Castillon
Miguel BERNUS
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Universitat Rovira i Virgili URV
Fundacio Eurecat
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Universitat Rovira i Virgili URV
Fundacio Eurecat
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Publication of EP4178950A1 publication Critical patent/EP4178950A1/fr
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Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D275/00—Heterocyclic compounds containing 1,2-thiazole or hydrogenated 1,2-thiazole rings
    • C07D275/04—Heterocyclic compounds containing 1,2-thiazole or hydrogenated 1,2-thiazole rings condensed with carbocyclic rings or ring systems
    • C07D275/06—Heterocyclic compounds containing 1,2-thiazole or hydrogenated 1,2-thiazole rings condensed with carbocyclic rings or ring systems with hetero atoms directly attached to the ring sulfur atom
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B45/00—Formation or introduction of functional groups containing sulfur
    • C07B45/06—Formation or introduction of functional groups containing sulfur of mercapto or sulfide groups
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
    • C07C311/01—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms
    • C07C311/02—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton
    • C07C311/03—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton having the nitrogen atoms of the sulfonamide groups bound to hydrogen atoms or to acyclic carbon atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
    • C07C311/15—Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings
    • C07C311/16—Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the sulfonamide groups bound to hydrogen atoms or to an acyclic carbon atom
    • C07C311/17—Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the sulfonamide groups bound to hydrogen atoms or to an acyclic carbon atom to an acyclic carbon atom of a hydrocarbon radical substituted by singly-bound oxygen atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
    • C07C311/50—Compounds containing any of the groups, X being a hetero atom, Y being any atom
    • C07C311/52—Y being a hetero atom

Definitions

  • the present invention relates to a family of reagents for polyfluoroalkylthiolation reactions. More specifically, it refers to a group of compounds useful for the transfer of polyfluoroalkylthiol groups of at least two carbons atoms into a great variety of organic compounds.
  • the invention also relates to the process for their preparation as well as to their use as reagents for polyfluorolakythiolation reactions.
  • the invention is also directed to the method for the polyfluoroalkylthiolation of an organic compound with the reagents of the invention.
  • fluoroalkyl motifs have been one of the pillars of synthetic, medicinal and crop chemistry due to the special attributes they confer to organic molecules. Increased lipophilicity, reinforced metabolic stability and improved ability to cross cell membranes and blood-brain barrier are some of the features benefited by these motifs [a) Ojima, I. In Fluorine in Medicinal Chemistry and Chemical Biology, Wiley-Blackwell, Chichester, 2009; b) Begue, J.-P.; Bonnet-Delpon, D. Bioorganic and Medicinal Chemistry of Fluorine; Wiley; Hoboken, 2008; c) Kirsch, P. Modern Fluoroorganic Chemistry: Synthesis, Reactivity, Applications; Wiley-VCH. Weinheim, 2004].
  • fluoroalkyl-containing thioethers have been on the spotlight since not only show outstanding Hansch lipophilicity (e.g. CF 3 , 0.88 VS SCF 3 , 1.44) [Bootwicha, T.; Liu, X; Pluta, R.; Atodiresei, I.; Rueping, M. Angew. Chem. Int. Ed. 2013, 52, 12856- 12859], but also serve as pivotal groups to access to other appreciated derivatives as fluorinated sulfoxides, sulfones or sulfonamides.
  • WO Patent WO2011097421 2011] Langlois [a) Ma, J.-J.; Yi, W.-B.; Lu, G.-P.; Cai, C. Catal. Sci. Technol. 2016, 6, 417-421; b) Ma, J.; Liu, Q.; Lu, G.; Yi, W. J. Fluorine Chem. 2017, 193, 113-117] and Umemoto reagents [a) Mei, B.; Zhang, P.; Li, Y. CN Patent, CN107540655, 2018; b) Kamiyama, H.; Itoh, S. WO Patent, WO2009014267, 2009; c) Verhoog, S.; Kee, C.
  • C-SCF 3 disconnection reveals a trifluoromethylthiolation process, typically addressed via direct late-stage modification using predefined SCF3 transfer agents, avoiding pre- functionalization steps and increasing the flexibility of the system [Barata-Vallejo, S.; Bonesi, S.; Postigo, A. Org. Biomol. Chem. 2016, 14, 7150–7182.].
  • This latter approach also for the introduction of SCF2H motif [Zhu, D.; Gu, Y.; Lu, L.; Shen, Q. J. Am. Chem.
  • Soc.2015, 137, 10547–10553.] has flourished the field with numerous protocols and reagents mostly based on imide, sulfonamide or sulfimide structures [a) Xu, C.; Ma, B.; Shen, Q. Angew. Chem. Int. Ed.2014, 53, 9316 –932; b) Alazet, S.; Ollivier, K.; Billard, T. Beilstein J. Org. Chem.2013, 9, 2354–2357; c) Xu, C.; Shen, Q. Org. Lett.2014, 16, 2046-2049; d) Billard, T.; Alazet, S.
  • SCF 2 CF 2 H or SCH 2 CF 2 H may introduce new opportunities for enabling hydrogen-bonding interactions, which role has been demonstrated to be critical in the mode of action of CF 2 H-derived ingredients [Zafrani, Y.; Yelle, D.; Sod-Moriah, G.; Hopkins, A.; Amir, D.; Marciano, D.; Gershonov E.; Saphier, S. J. Med. Chem. 2017, 60, 797 ⁇ 804; Chem. Commun.; 2019, 55, 12487–12490; J. Am. Chem. Soc.2017, 139, 27, 9325–9332.].
  • FIGURES Figure 1: Reaction of the electrophilic reagent according to the invention (compound 3a) with N-H-indole in various solvents.
  • Figure 2 a) state-of-the-art preparation of electrophilic trifluoromethylthiolation reagents; b) failed attempts to prepare longer polyfluoroalkylthiolation reagents; c) approach for the synthesis of reagents according to the invention.
  • Rf represents polyfluoroalkyl chain from 2 to 10 carbon atoms.
  • Figure 3 Preparation of polyfluoroalkyl thiol electrophilic reagents according to the invention.
  • Figure 4 Polyfluoroalkylthiolation of different chemical species with a compound according to the invention (compound 3a).
  • Figure 5 Reaction of various electrophilic reagents according to the invention with N-H indole. Yields are calculated by 19 F NMR using 1,4-difluorobenzene as internal standard.
  • OBJECT OF THE INVENTION The present invention discloses novel compounds that show a high efficiency in the transfer of polyfluoroalkyl thiols of two or more carbon atoms in a variety of organic molecules.
  • the main aspect of the present invention is related to compounds of general formula (I): wherein: the dotted line represents an optional bond; Z is -CO- or -SO 2 - ; G 1 represents a group –[CH 2 ] n -R 1 ; G 2 represents a group –[CH 2 ] m -R 2 ; or G 1 together with G 2 form a fused or non-fused aromatic or heteroaromatic ring optionally substituted by one or more R 3 substituents; n and m are 0 or 1; x is an integer between 2 and 10; y is an integer between 1 and 21 but always lower than (2x+1) R 1 and R 2 are independently from one another a hydrogen atom, a C 1-6 alkyl, a phenyl ring optionally substituted by one or more R 3 substituents; R3 is
  • Another object of the invention refers to the use of such compounds of general formula (I) as reactive for the polyfluoroalkylthiolation of organic compounds.
  • a method for the polyfluoroalkylthiolation of an organic compound that comprises reacting a compound according to formula (I) with said organic compound.
  • a first and main aspect of the invention is a compound of general formula (I): wherein: the dotted line represents an optional bond; Z is -CO- or -SO 2 - ; G 1 represents a group –[CH 2 ] n -R 1 ; G 2 represents a group –[CH 2 ] m -R 2 ; or G 1 together with G 2 form a fused or non-fused aromatic or heteroaromatic ring optionally substituted by one or more R 3 substituents; n and m are 0 or 1; x is an integer between 2 and 10; y is an integer between 1 and 21 but always lower than (2x+1) R1 and R2 are independently from one another a hydrogen atom, a C1-6 alkyl, a phenyl ring optionally substituted by one or more R3 substituents; R 3 is a hydrogen atom, a C 1-6 alkyl, a C 1-6 alkoxy, halogen atom, a
  • Halogen or “halo” as referred in the present invention represents fluorine, chlorine, bromine or iodine.
  • halo represents fluorine, chlorine, bromine or iodine.
  • substituents such as for instance “C 1-6 haloalkyl” or “C 1-6 haloalkoxy” it means that the alkyl or alkoxy radical can respectively contain at least one halogen atom.
  • C1-6 alkyl as referred to in the present invention, are saturated aliphatic radicals. They may be linear (unbranched) or branched and may be optionally substituted.
  • C1-6-alkyl as expressed in the present invention means an alkyl radical of 1, 2, 3, 4, 5 or 6 carbon atoms.
  • Preferred alkyl radicals according to the present invention include but are not restricted to methyl, ethyl, propyl, n-propyl, isopropyl, butyl, n-butyl, tert-butyl, isobutyl, sec-butyl, 1-methylpropyl, 2-methylpropyl, 1,1-dimethylethyl, pentyl, n-pentyl, 1,1- dimethylpropyl, 1,2-dimethylpropyl, 2,2-dimethylpropyl, hexyl or 1-methylpentyl.
  • the most preferred alkyl radical are C1-4 alkyl, such as methyl, ethyl, propyl, n-propyl, isopropyl, butyl, n-butyl, tert-butyl, isobutyl, sec-butyl, 1-methylpropyl, 2-methylpropyl or 1,1-dimethylethyl.
  • Alkyl radicals are optionally mono- or polysubstituted by substitutents independently selected from a halogen atom, a C1-6- alkoxy radical, a C1-6-alkyl radical, a C1-6-haloalcoxy radical, a C1-6-haloalkyl radical, CN, a trihaloalkyl radical and a hydroxyl group.
  • C1-6 alkoxy as referred to in the present invention, is understood as meaning an alkyl radical/group as defined above attached via an oxygen linkage to the rest of the molecule. Examples of alkoxy include, but are not limited to methoxy, ethoxy, propoxy, butoxy or tert-butoxy.
  • Aromatic ring as referred to in the present invention, is understood as meaning cyclic system formed by a single aromatic ring without heteroatoms. It can also be a fused system with at least one additional ring system that can be either aromatic or not. Aromatic rings may optionally be mono- or polysubstituted by substitutents independently selected from a halogen atom, a C 1-6 -alkyl radical, a C 1-6 -alkoxy radical, a C 1-6 -haloalcoxy radical, a C 1-6 -haloalkyl radical and a hydroxyl group.
  • non-fused and fused aromatic ring include but are not restricted to phenyl, naphthyl, fluoranthenyl, fluorenyl, tetralinyl, indanyl or anthracenyl radicals, which may optionally be mono- or polysubstituted, if not defined otherwise. More preferably aromatic rings in the context of the present invention are 6-membered ring systems, optionally at least monosubstituted. “Heteroaromatic ring” as referred to in the present invention, is understood as meaning heterocyclic system formed by a single aromatic ring that contains one or more heteroatoms from the group consisting of N, O and S.
  • Heteroaromatic rings may optionally be mono- or polysubstituted by substituents independently selected from a halogen atom, a C1-6-alkyl radical, a C1-6-alkoxy radical, a C1-6-haloalkoxy radical, a C1-6-haloalkyl radical and a hydroxyl group.
  • non-fused and fused heteroaromatic ring include but are not restricted to furan, benzofuran, thiophene, thiazole, pyrrole, pyridine, pyrimidine, pyridazine, pyrazine, quinoline, isoquinoline, phthalazine, triazole, pyrazole, imidazole, imidazo[4,5-b]pyridine, isoxazole, oxadiazole, indole, benzotriazole, benzodioxolane, benzodioxane, benzimidazole, carbazole or quinazoline.
  • heteroaromatic ring in the context of the present invention are 5- or 6-membered ring systems, optionally at least monosubstituted.
  • Salt is to be understood as meaning any form of the compound of formula (I) according to the invention in which it assumes an ionic form or is charged and is coupled with a counter-ion (a cation or anion) or it is in solution.
  • a counter-ion a cation or anion
  • “Solvate” is to be understood as meaning any form of the compound of formula (I) according to the invention in which this compound interacts via non-covalent binding another molecule (most likely a polar solvent) especially including hydrates and alcoholates, e.g. methanolate.
  • “Leaving group” is an atom or a molecular entity that in a heterolytic bond cleavage keeps the electron pair of the bond. Suitable leaving groups are well known in the art and include Cl, Br, I and -O-SO 2 R’, wherein R’ is F, C 1-4 -alkyl, C 1-4 -haloalkyl, or optionally substituted phenyl.
  • the preferred leaving groups are Cl, Br, I, tosylate, mesylate, nosylate, triflate, nonaflate and fluorosulphonate.
  • n and m are 0.
  • a proviso is applicable to compounds of formula (I) by means of which when n is 0 and/or m is 0 while at the same time that Z is -SO 2 -, then R 1 and R 2 are not H.
  • R 1 and R 2 are independently from one another a C 1-6 alkyl, preferably a methyl; or a phenyl ring.
  • n and m are 0 and R1 and R2 are independently from one another a C1-6 alkyl, preferably a methyl or a phenyl ring.
  • R1 and R2 are independently from one another a C1-6 alkyl, preferably a methyl or a phenyl ring.
  • Yet another particular and preferred embodiment of the invention is represented by compounds of formula (I) where G1 together with G2 form a benzene ring optionally substituted by one or more R3 substituents.
  • x may represent in the compounds of formula (I) an integer starting from 2 and up to 10, in a particular a preferred embodiment x is 2, 3, 4 or 5. Under this preferred embodiment, y may be represented an integer going from 1 to a maximum of 10 when x is 5.
  • the compounds of formula (I) have one of the following subformulas: wherein Z, R 1 , R 2 , R 3 , x and y are as defined before for formula (I).
  • the compounds of the invention show one of the following subformulas: wherein R 1 , R 2 , R 3 , x and y are as defined before for formula (I).
  • the compounds of the present invention are suitable for the transfer of polyfluoroalkylthiol groups of two or more carbon atoms.
  • the groups transferred in the fluoroalkylthiolation reaction are those represented by the moiety -S[CxFyH(2x+1-y)] of the compounds of formula (I).
  • the -S[C x F y H (2x+1-y) ] moiety in the compounds of formula (I) is represented by one of the followings: -SCH 2 CF 3 -SCH 2 CF 2 H -SCF 2 CF 2 H -SCF 2 CF 3 -SCH 2 (CF 2 ) 3 CF 2 H -S(CF 2 ) 3 CF 3 -SCF(CF 3 ) 2
  • the preferred embodiments of the invention are represented by the following reagents of formula (I): ⁇ 2-((1,1,2,2-Tetrafluoroethyl)thio)benzo[d]isothiazol-3(2H)-one 1,1-dioxide; ⁇ 6-Nitro-2-((1,1,2,2-tetrafluoroethyl)thio)benzo[d]isothiazol-3(2H)-one 1,1-dioxide; ⁇ N-(phenylsulfonyl)-
  • the compounds of the present invention have shown to be very stable in different solvents such as acetonitrile (ACN), Toluene, tetrahydrofuran (THF) and 1,2- dichloroethane (DCE). They have also shown to be very effective in the transfer of polyfluoroalkylthiol groups under varied conditions. For instance, the tolerance and robustness of the reagents has been proved by performance of the polyfluoroalkylthiolation reaction in solvents of very different nature (chlorinated, protic, aprotic polar and aprotic non-polar solvents) as shown in figure 1.
  • solvents such as acetonitrile (ACN), Toluene, tetrahydrofuran (THF) and 1,2- dichloroethane (DCE). They have also shown to be very effective in the transfer of polyfluoroalkylthiol groups under varied conditions. For instance, the tolerance and robustness of the reagents has been proved by performance of the polyfluor
  • the invention refers to a process for producing a compound of general formula (I) comprising the reaction of a compound of formula (II) or a salt thereof: with a compound of formula (III): wherein Z, G1, G2, x and y are as defined in claim 1 and X is a suitable leaving group, preferably a halogen group, more preferably a chlorine.
  • the process for producing the compounds of formula (I) can be carried out in a suitable aprotic solvent, preferably in a solvent such as CH2Cl2 (DCM), chloroform, DCE or diethyl ether.
  • the reaction is preferably carried out at a temperature between -30oC and 50oC more preferably between 0oC and 30 oC.
  • the process for the preparation of the reagents of formula (I) of the present invention was developed after some reported failed approaches for the preparation of polyfluoroalkyl reagents of 2 or more carbon atoms (see figure 2b).
  • the present invention was able to solve the problem of providing reagents for the transfer of polyfluoroalkyl thiol groups with long alkyl chains (from 2 to 10 carbons) by means of a new and effective approach (see figure 2c).
  • RfCH2SCl compounds are prepared via tosylation/thioacetylation sequence from the corresponding alcohols followed by cleavage of the acyl group and further halogenation, preferably chlorination.
  • RfSCl compounds bearing fluorines on the ⁇ -carbon can be synthetized by preparation of benzyl thioether and further halogenation, preferably chlorination.
  • benzyl thioether and further halogenation preferably chlorination.
  • a variety of fluoroalkyl chains, with different fluorination grade and number of carbons to show the generality and validity of this approach have been prepared. The detailed synthesis of each sulfenyl chloride is described later in the experimental section.
  • intermediates of formula (II) can either be commercially purchased or produced by methods commonly known to a skilled person.
  • the intermediate of formula (II) is reacted in the form of a suitable salt, preferably as a potassium, sodium or silver salt.
  • Another aspect of the invention is related to the use of compound of formula (I) according to the invention as reagent for the polyfluoroalkylthiolation of organic compounds.
  • the reagents of the present invention are useful in the transfer of polyfluoroalkylthiol groups into a great variety of chemical species (see figure 4) proving the versatility of the compounds of the invention.
  • the compounds of formula (I) are especially suited for polyfluoroalkylthiolation of organic compounds selected from alcohols, amines, thiols, phosphines, 1,3-dicarbonylic compounds, ketones, phenols, enol ethers, aromatic heterocycles, alkenes, alkynes or organometallic compounds.
  • Figure 5 represents the high yield obtained in the transfer reaction of different polyfluoroalkyl thiol groups into N-H-indole and the reaction conditions in each case.
  • a final aspect of the inventions somehow connected to the previous one is a method for the polyfluoroalkylthiolation of an organic compound that comprises reacting a reagent of formula (I) according to the invention with said organic compound.
  • the polyfluoroalkylthiolation method is carried out over an organic compound selected from alcohols, amines, thiols, phosphines, 1,3- dicarbonylic compounds, ketones, phenols, enol ethers, aromatic heterocycles, alkenes, alkynes or organometallic compounds.
  • organic compound selected from alcohols, amines, thiols, phosphines, 1,3- dicarbonylic compounds, ketones, phenols, enol ethers, aromatic heterocycles, alkenes, alkynes or organometallic compounds.
  • TMSCl trimethylsilyl chloride
  • Brine refers to a saturated solution of sodium chloride.
  • Anhydrous sodium sulfate (Na 2 SO 4 ) was used as drying agent after reaction work-up, as indicated. All reagents were purchased from Sigma Aldrich, Cymit, Carbosynth, Apollo Scientific, Fluorochem and Manchester Organics chemical companies.
  • EXAMPLE 1 PREPARATION OF INTERMEDIATE COMPOUNDS
  • Example 1a synthesis of ⁇ -fluorinated intermediates The synthesis of polyfluoroalkylsulfenyl chlorides with fluorinated ⁇ -methylene groups (RCF2SCl) was performed following the protocols depicted in scheme 1.
  • Benzyl(perfluoroethyl)sulfane (18b) A flask containing KF (3.31 g, 56.97 mmol, 1.2 eq.) and KSCN (6.92 g, 71.2 mmol, 1.5 eq.) was evacuated and backfilled with argon three times followed by sequential addition of dry ACN (23 mL), benzyl bromide (5.64 mL, 47.47 mmol, 1 eq.) and TMSCF2CF3 (10 mL, 56.97 mmol, 1.2 eq.). The mixture was stirred under argon at 100 oC for 2 hours.
  • Benzyl(perfluorobutyl)sulfane (18d) A Schlenk flask charged with benzyl thiocyanate (4.97 g, 33.3 mmol, 1 eq.) was evacuated and backfilled with argon three times. Dry pyridine (30 mL) and 1,1,1,2,2,3,3,4,4-nonafluoro-4-iodobutane (11.46 mL, 66.6 mmol, 2 eq.) were sequentially added under argon atmosphere and the mixture was cooled to 0 oC using an ice/water bath.
  • Zinc dust (3.26 g, 49.95 mmol, 1.5 eq.) was added and the mixture stirred 30 minutes at 0 oC and 17 h at room temperature. Another portion of Zn dust (5.0 g, 76.47 mmol, 2.3 eq.) was added at 0 oC under vigorous stirring and after 30 minutes, the temperature was increased to room temperature and stirred for 5 h. The mixture was then diluted with Et 2 O (100 mL) and acidified with 10% aqueous HCl (50 mL) and transferred to an extraction funnel.
  • Benzyl(perfluoropropan-2-yl)sulfane (18c) A Schlenk flask charged with benzyl thiocyanate (750 mg, 5.0 mmol, 1 eq.) was evacuated and backfilled with argon three times. Dry pyridine (5 mL) and 1,1,1,2,3,3,3- heptafluoro-2-iodopropane (1.40 mL, 10 mmol, 2.0 eq.) were sequentially added under argon atmosphere and the mixture was cooled to 0 oC using an ice/water bath.
  • Zinc dust 500 mg, 7.5 mmol, 1.5 eq. was added and the mixture stirred for 30 minutes at 0 oC and 20 h at room temperature. The mixture was then diluted with Et 2 O (30 mL) and acidified with 10% aqueous HCl (20 mL) and transferred to an extraction funnel. The aqueous layer was separated, and the organic phase was further washed with 10% aqueous HCl (3 x 5 mL), saturated aqueous NaHCO 3 (3 x 10 mL) and brine (10 mL). The organic fraction was dried with Na 2 SO 4 , filtrated and the solvent concentrated under reduced pressure.
  • Example 1b synthesis of non- ⁇ -fluorinated intermediates (RfCH2SCl chains) 1 Kunshenko, B. V.; Omarov, V. O.; Muratov, N. N.; Yagupol'skii, L. M. Zh. Org. Khim.1992, 28, 892– 900. 2 Abe, T., Shreeve, J. M. J. Fluorine Chem.1973, 3, 187-196. 3 Harris, J. F. J. Org. Chem.1979, 444, 563-569. 4 Sizov, A. Y., Kovregin, A. N., Serdyuk, R. N., Vorob’ev, M.
  • the reaction mixture was cooled to 0 oC and acidified using 10% aqueous HCl (500 mL) under vigorous stirring. After 15 minutes, the mixture was transferred to an extraction funnel, additional water (500 mL) was added and the organic layer was separated. The aqueous phase was extracted with three portions of DCM (3 x 200 mL) and the combined organic fractions were dried with Na2SO4, filtrated and the solvent evaporated under reduced pressure. The obtained crude product (240 g, 94% yield) was used in the next step without further purification.
  • the reaction mixture was cooled to 0 oC and acidified using 10% aqueous HCl (100 mL) under vigorous stirring. After 15 minutes, the mixture was transferred to an extraction funnel, additional water (100 mL) was added and the organic layer was separated. The aqueous phase was extracted with three portions of DCM (3 x 100 mL) and the combined organic fractions were dried with Na2SO4, filtrated and the solvent evaporated under reduced pressure. The obtained crude product (39.8 g, 92% yield) was used in the next step without further purification.
  • the reaction mixture was cooled to 0 oC and acidified using 10% aqueous HCl (100 mL) under vigorous stirring. After 15 minutes, the mixture was transferred to an extraction funnel, additional water (100 mL) was added and the organic layer was separated. The aqueous phase was extracted with three portions of DCM (3 x 100 mL) and the combined organic fractions were dried with Na 2 SO 4 , filtrated and the solvent evaporated under reduced pressure. The obtained crude product (112.5 g, 93% yield) was used in the next step without further purification.
  • 2,2,2-Trifluoroethane-1-thiol (21e): A 250 mL round-bottom flask, equipped with a magnetic stir bar, was charged with sodium metal (0.22 g, 0.94 mmol, 0.05 eq.). The flask was then evacuated and backfilled with argon three times. Subsequently, 94 mL of ethylene glycol were added. Next, S- (2,2,2-trifluoroethyl) ethanethioate (20e) (2.96 g, 18.7 mmol, 1.0 eq.) was added to the mixture. Then, the reaction mixture stirred overnight at room temperature.
  • the flask was then evacuated and backfilled with argon three times. Subsequently, 11.5 mL of anhydrous DCM were added using a syringe. Then, a current of chlorine gas was passed through the solution for 15 minutes. Then, the reaction mixture was concentrated under reduced pressure and redissolved in 5 mL of anhydrous DCM. An aliquot was transferred to an NMR tube and quantitative NMR analysis that indicated a concentration of 0.69 M of 2,2,3,3,4,4,5,5-octafluoropentanesulfenyl chloride (20f) in DCM.
  • 2,2-Difluoroethylsulfenyl chloride 22g: A 100 mL round-bottom flask, equipped with a magnetic stir bar was charged with S- (2,2-difluoroethyl) ethanethioate (20g) (8.8 g, 63 mmol, 1.0 eq.). The flask was then evacuated and backfilled with argon three times. Subsequently, 60 mL of anhydrous DCE were added using a syringe. Then, a current of chlorine gas was passed through the solution for 15 minutes.
  • EXAMPLE 2 PREPARATION OF THE REAGENTS OF FORMULA (I) 2-((1,1,2,2-Tetrafluoroethyl)thio)benzo[d]isothiazol-3(2H)-one 1,1-dioxide (3a): A 5 mL round-bottom flask, equipped with a magnetic stir bar, was charged with potassium saccharin salt (221 mg, 1.5 mmol, 1.5 eq.). The flask was then evacuated and backfilled with argon three times. Subsequently, 1.6 mL of anhydrous CHCl 3 were added using a syringe.
  • N-(phenylsulfonyl)-N-((1,1,2,2-tetrafluoroethyl)thio)benzamide (5a): A 10 mL round-bottom flask, equipped with a magnetic stir bar, was charged with potassium N-(phenylsulfonyl)benzamide salt (790 mg, 2.64 mmol, 1.3 eq.). The flask was then evacuated and backfilled with argon three times. Subsequently, 5 mL of anhydrous CHCl3 were added using a syringe.
  • N-(methylsulfonyl)-N-((perfluoroethyl)thio)methanesulfonamide (6a): A 10 mL round-bottom flask, equipped with a magnetic stir bar, was charged with potassium N-(methylsulfonyl)methanesulfonamide salt (558 mg, 2.64 mmol, 1.3 eq.). The flask was then evacuated and backfilled with argon three times. Subsequently, 5 mL of anhydrous CHCl 3 were added using a syringe.
  • EXAMPLE 3 POLYFLUOROALKYLTHIOLATION REACTIONS 3-((1,1,2,2-tetrafluoroethyl)thio)-1H-indole (8a): Protocol A: using reagent 3a An 8 mL reaction vial, equipped with a magnetic stir bar, was charged with 1H-indole (35 mg, 0.3 mmol, 1.0 eq.). The flask was then evacuated and backfilled with argon three times. Subsequently, 1.5 mL of anhydrous DCM were added using a syringe.
  • reagent 3a (104 mg, 0.33 mmol, 1.1 eq.) was added to the flask and the mixture was stirred for 1 hour at 40 oC.
  • the reaction mixture was diluted with DCM, washed with NaHCO 3 (saturated) and dried over MgSO 4 .
  • the organic layer was concentrated under reduced pressure and purified by flash column chromatography (silica gel, 2:8 Ethyl acetate/hexane) to afford the desired product as a white solid (71 mg, 95% yield).
  • Protocol B using reagent 6a
  • 1H-indole 35 mg, 0.3 mmol, 1.0 eq.
  • the flask was then evacuated and backfilled with argon three times.
  • 1.5 mL of anhydrous DCM were added using a syringe.
  • reagent 6a 101 mg, 0.33 mmol, 1.1 eq.
  • the reaction mixture was diluted with DCM, washed with aqueous NaHCO 3 and dried over MgSO 4 .
  • reagent 3a 41 mg, 0.13 mmol, 1.3 eq.
  • trimethylsilyl chloride 25 ⁇ l, 0.2 mmol, 2.0 eq.
  • the mixture was stirred for 16 hours at 80 oC.
  • the flask was then evacuated and backfilled with argon three times. Subsequently, 0.6 mL of anhydrous ACN were added using a syringe. The mixture was stirred for 16 hours at 80 oC.
  • Diethyl 2-benzyl-2-((1,1,2,2-tetrafluoroethyl)thio)malonate (13a): Protocol A: using reagent 3a A 5 mL round-bottom flask, equipped with a magnetic stir bar, was charged with NaH (60% in mineral oil, 9 mg, 0.23 mmol, 1.5 eq.). The flask was then evacuated and backfilled with argon three times. Subsequently, 1.5 mL of anhydrous THF were added using a syringe followed by diethyl 2-benzylmalonate (35.5 ⁇ l, 0.15 mmol, 1.0 eq.) and the mixture is stirred at room temperature for 15 minutes.
  • reagent 3a (118 mg, 0.38 mmol, 1.7 eq.) was quickly added to the flask and the mixture was stirred for 15 minutes at room temperature.
  • the reaction mixture was diluted with Et2O, washed with NH4Cl (saturated) and dried over MgSO4. Upon filtration, the organic layer was concentrated under reduced pressure and purified by flash column chromatography (silica gel, 9:1 hexane/ethyl acetate) to afford the desired product as a colorless oil (51 mg, 88% yield).
  • Protocol B using reagent 6a
  • reaction mixture was diluted with Et 2 O, washed with NH 4 Cl (saturated) and dried over MgSO 4 . Upon filtration, the organic layer was concentrated under reduced pressure and purified by flash column chromatography (silica gel, 9:1 hexane/ethyl acetate) to afford the desired product as a colorless oil (47 mg, 81% yield).
  • reaction mixture was diluted with Et2O, washed with NaHCO3 (saturated) and dried over MgSO4. Upon filtration, the organic layer was concentrated under reduced pressure and purified by flash column chromatography (silica gel, 9:1 hexane/ethyl acetate) to afford the desired product as a yellow oil (66 mg, 97% yield).
  • reaction mixture was diluted with DCM, filtered through Celite® washed with H 2 O, brine and dried over MgSO 4 . Upon filtration, the organic layer was concentrated under reduced pressure and purified by flash column chromatography (silica gel, 9:1 hexane/ethyl acetate) to afford the desired product as a colorless oil (44 mg, 80% yield).

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Abstract

La présente invention concerne un groupe de composés de formule (I) utile pour le transfert de groupes polyfluoroalkylthiol d'au moins deux atomes de carbone dans une grande variété de composés organiques, ainsi qu'un procédé pour leur préparation. L'invention concerne également un procédé de polyfluoroalkylthiolation d'un composé organique avec les réactifs selon l'invention.
EP21737060.0A 2020-07-07 2021-06-28 Réactifs pour polyfluoroalkylthiolation de composés organiques et procédé de production associé Pending EP4178950A1 (fr)

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DE3313718A1 (de) * 1983-04-15 1984-10-18 Bayer Ag, 5090 Leverkusen N-sulfenylierte phenethylsulfonamide
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WO2011097421A1 (fr) 2010-02-03 2011-08-11 Meh Associates, Inc Fluorométhanes à substitutions multiples en tant qu'isostères sélectifs et bioactifs
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