WO2011070131A1 - 5-amino-4-hydroxypentoylamides - Google Patents

5-amino-4-hydroxypentoylamides Download PDF

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WO2011070131A1
WO2011070131A1 PCT/EP2010/069328 EP2010069328W WO2011070131A1 WO 2011070131 A1 WO2011070131 A1 WO 2011070131A1 EP 2010069328 W EP2010069328 W EP 2010069328W WO 2011070131 A1 WO2011070131 A1 WO 2011070131A1
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mmol
compound
precursor
solution
formula
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PCT/EP2010/069328
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Inventor
Genadiy Kalayanov
Bart Rudolf Romanie Kesteleyn
Kevin Parkes
Bengt Bertil Samuelsson
Wim Bert Griet Schepens
Johannes Wilhelmus J. Thuring
Hans Kristian Wallberg
Jörg Kurt WEGNER
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Tibotec Pharmaceuticals
Medivir Ab
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Priority to UAA201205119A priority Critical patent/UA108744C2/ru
Priority to EA201290487A priority patent/EA020758B1/ru
Priority to US13/515,187 priority patent/US8592429B2/en
Priority to JP2012542555A priority patent/JP5797662B2/ja
Priority to DK10790938.4T priority patent/DK2509950T3/en
Priority to NZ599916A priority patent/NZ599916A/xx
Priority to ES10790938.4T priority patent/ES2536774T3/es
Priority to CN201080055694.9A priority patent/CN102770413B/zh
Priority to BR112012013493-0A priority patent/BR112012013493B1/pt
Priority to KR1020127017093A priority patent/KR101771698B1/ko
Application filed by Tibotec Pharmaceuticals, Medivir Ab filed Critical Tibotec Pharmaceuticals
Priority to EP10790938.4A priority patent/EP2509950B1/fr
Priority to PL10790938T priority patent/PL2509950T3/pl
Priority to MX2012006613A priority patent/MX2012006613A/es
Priority to AP2012006228A priority patent/AP3217A/xx
Priority to CA2783929A priority patent/CA2783929C/fr
Priority to AU2010329867A priority patent/AU2010329867B2/en
Priority to SG2012042552A priority patent/SG181609A1/en
Publication of WO2011070131A1 publication Critical patent/WO2011070131A1/fr
Priority to IL219272A priority patent/IL219272A/en
Priority to HK13104373.4A priority patent/HK1177454A1/xx

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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D213/62—Oxygen or sulfur atoms
    • C07D213/63—One oxygen atom
    • C07D213/64—One oxygen atom attached in position 2 or 6
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12—Antivirals
    • A61P31/14—Antivirals for RNA viruses
    • A61P31/18—Antivirals for RNA viruses for HIV
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D213/72—Nitrogen atoms
    • C07D213/74—Amino or imino radicals substituted by hydrocarbon or substituted hydrocarbon radicals
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
    • C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
    • C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D277/22—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
    • C07D277/30—Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
    • C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D493/00—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system
    • C07D493/02—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system in which the condensed system contains two hetero rings
    • C07D493/04—Ortho-condensed systems

Definitions

  • This invention concerns 5-amino-4-hydroxy-pentoyl amides having HIV (Human Immunodeficiency Virus) replication inhibiting properties, the preparation thereof and pharmaceutical compositions comprising these compounds.
  • HIV Human Immunodeficiency Virus
  • HAA T Highly Active Anti-Retroviral Therapy
  • NRTI non-nucleoside reverse transcriptase inhibitor
  • PI protease inhibitor
  • HIV protease inhibitors that are more effective in terms of activity against wild type virus, but also against mutated strains, in particular toward mutated strains selected by the currently approved protease inhibitors.
  • protease inhibitors that are beneficial in terms of their pharmacokinetical profile, in particular that exhibit reduced plasma protein binding.
  • the present invention is aimed at providing particular novel series of 5-amino-4- hydroxy-pentoyl amides having HIV replication inhibiting properties.
  • the compounds of the invention differ from prior art compounds in structure, pharmacological activity and/or pharmacological potency. It has been found that they not only are very active against wild type virus, but also against mutant strains, in particular against strains that have become resistant to one or more known protease inhibitors, which strains are referred to as drug- or multidrug-resistant HIV strains.
  • the present invention concerns compounds of formulae I, including the stereo chemically isomeric forms thereof, which can be represented by formula I:
  • R 1 is halo, Ci_ 4 alkoxy, trifluoromethoxy
  • R 2 is a group of formula:
  • R 3 is a group of formula:
  • R 4 is a group of formula:
  • n 0 or 1 ;
  • each A independently is CH or N;
  • R 5 and R 6 independently are hydrogen, Ci_ 4 alkyl, or halo;
  • R 7 is Ci_ 4 alkyl or Ci_ 4 alkoxyCi_ 4 alkyl
  • R 8 is Ci_ 4 alkyl or Ci_ 4 alkoxyCi_ 4 alkyl
  • each R 9 independently is Ci_ 4 alkyl, cyclopropyl, trifluoromethyl, Ci_ 4 alkoxy, or
  • R 10 is hydrogen, Ci_ 4 alkyl, cyclopropyl, trifluoromethyl, Ci_ 4 alkoxy, or dimethylamino;
  • R 11 is hydrogen or Ci_ 4 alkyl;
  • a bond with an asterisk represents the bond linking that fragment or group with the remainder of the molecule.
  • Ci_ 4 alkyl as a group or part of a group defines straight or branched chain saturated hydrocarbon radicals having from 1 to 4 carbon atoms such as methyl, ethyl, 1 -propyl, 2-propyl, 1 -butyl, 2-butyl, 2-methyl-propyl, t.butyl.
  • Ci_ 4 alkyl is Ci_ 3 alkyl or Ci_ 2 alkyl; Ci_ 3 alkyl defines straight or branched chain saturated hydrocarbon radicals having from 1 to 3 carbon atoms; Ci_ 2 alkyl defines methyl or ethyl.
  • halo is generic to fluoro, chloro, bromo or iodo, in particular to fluoro or chloro.
  • radical Whenever a radical occurs in the definition of the compounds of formula I or in any of the subgroups of compounds of formula I specified herein, said radical independently is as specified above in the definition of the compounds of formula I or in the more restricted definitions as specified hereinafter.
  • radical positions on any molecular moiety used in the definitions may be anywhere on such moiety as long as it is chemically stable.
  • radical R 1 may be on any position of the phenyl to which it is attached.
  • hydrochloric or hydrobromic acid sulfuric, hemisulphuric, nitric, phosphoric, and the like acids; or organic acids such as, for example, acetic, aspartic, dodecyl-sulphuric, heptanoic, hexanoic, nicotinic, propanoic, hydroxyacetic, lactic, pyruvic, oxalic, malonic, succinic, maleic, fumaric, malic, tartaric, citric, methanesulfonic, ethanesulfonic, benzene- sulfonic, /?-toluenesulfonic, cyclamic, salicylic, /?-amino-salicylic, pamoic, and the like acids.
  • said acid addition salt forms can be converted into the free base form by treatment with an appropriate base.
  • the compounds of formula I containing acidic protons may be converted into their pharmaceutically acceptable metal or amine addition salt forms by treatment with appropriate organic and inorganic bases.
  • Appropriate base salt forms comprise, for example, the ammonium salts, the alkali and earth alkaline metal salts, e.g. the lithium, sodium, potassium, magnesium, calcium salts and the like, salts with organic bases, e.g.
  • primary, secondary, and tertiary aliphatic and aromatic amines such as methylamine, ethylamine, propylamine, isopropylamine, the four butylamine isomers, dimethyl- amine, diethylamine, diethanolamine, dipropylamine, diisopropylamine, di-n-butyl- amine, pyrrolidine, piperidine, morpholine, trimethylamine, triethylamine, tripropyl- amine, quinuclidine, pyridine, quinoline and isoquinoline, the benzathine, N-methyl- D-glucamine, 2-amino-2-(hydroxymethyl)-l,3-propanediol, hydrabamine salts, and salts with amino acids such as, for example, arginine, lysine and the like.
  • the salt form can be converted by treatment with acid into the free acid form.
  • solvate is meant to comprise hydrates and solvent addition forms that the compounds of formula I, including stereoisomeric forms thereof, can form.
  • solvates are e.g. hydrates, alcoholates, such as ethanolates, i.propanolates, n.propanolates, and the like.
  • the compounds of formula I thereof may contain one or more centers of chirality and may exist as stereochemically isomeric forms. Of special interest are those compounds of formula I that are stereochemically pure.
  • stereochemically isomeric forms as used herein defines all the possible stereoisomeric forms of the compounds of formula I, the pharmaceutically acceptable addition salts thereof, and the
  • stereochemically isomeric forms said mixtures containing all diastereomers and enantiomers of the basic molecular structure as well as each of the individual isomeric forms of formula I, the pharmaceutically acceptable addition salts thereof, and the pharmaceutically acceptable solvates thereof substantially free, i.e. associated with less than 10%, preferably less than 5%, in particular less than 2% and most preferably less than 1% of the other isomers.
  • Stereogenic centers may have the R- or S-configuration; substituents on bivalent cyclic (partially) saturated radicals may have either the cis- or trans-configuration; double bonds can have an E (ent ought) or Z (zusammen)
  • the present invention is also intended to include any isotopes of atoms present in the compounds of the invention.
  • isotopes of hydrogen include tritium and deuterium and isotopes of carbon include 13 C and 14 C.
  • substituents can be selected each independently out of a list of definitions, such as for example for R 1 or R 2 , any possible combinations are intended to be included that are chemically possible or that lead to molecules of such chemical stability that they can be processed in standard pharmaceutical procedures.
  • R 1 is halo; or R 1 is fluoro or chloro; which halo (or fluoro or chloro) in particular is substituted in ortho position; or
  • R 1 is methoxy; which methoxy in particular is substituted in meta position.
  • R 2 is a group of formula
  • R 5 is hydrogen, and R 6 is halo or Ci_ 4 alkyl; R 5 is halo and R 6 is hydrogen; R 5 is halo or Ci_ 4 alkyl, and R 6 is hydrogen; or R 5 and R 6 are both hydrogen, or are both halo.
  • Particular embodiments of the present invention are those compounds of formula I or any of the subgroups of compounds of formula I, including the compounds wherein R 2 is as defined above under (a) or (b), wherein R 5 is hydrogen and R 6 is fluoro or chloro; R 5 is fluoro or chloro and R 6 is hydrogen; R 5 is hydrogen and R 6 is methyl; R 5 and R 6 are both hydrogen, or R 5 is chloro and R 6 is fluoro; more in particular wherein R 5 is hydrogen and R 6 is fluoro; R 5 is chloro and R 6 is hydrogen; R 5 is hydrogen and R 6 is methyl; R 5 and R 6 are both hydrogen, R 5 is chloro and R 6 is fluoro, R 5 is methyl and R 6 is fluoro, or R 5 is fluoro and R 6 is methyl.
  • Embodiments of the present invention are those compounds of formula I or any of the subgroups of compounds of formula I wherein R 3 is a group of formula
  • a further embodiment concerns those compounds of the invention wherein R 3 is a group of formula
  • R 8 is methyl or 2-methoxyethyl; or wherein R 8 is methyl.
  • Embodiments of the present invention are those compounds of formula I or any of the subgroups of compounds of formula I wherein
  • R 9 is Ci_ 2 alkoxy or dimethylamino; or R 9 is methoxy or dimethylamino; or R 9 is
  • Embodiments of the present invention are those compounds of formula I or any of the subgroups of compounds of formula I wherein
  • R 4 is a group having the chemical structure specified above, but wherein in the first group R 9 is R 9a in the second group R 9 is R 9b in the third group R 9 is R 9c in the fourth group R 9 is R 9d in the fifth and in the sixth group R 9 is R 9e ; which groups therefore can be represented as follows:
  • each A independently is CH or N; or wherein each A is CH;
  • R 9a is Ci_ 4 alkoxy or dimethylamino
  • R 9b is Ci_ 4 alkoxy or dimethylamino
  • R 9c is Ci_ 4 alkoxy or dimethylamino
  • R 9d is Ci_ 4 alkyl, cyclopropyl, trifluoromethyl
  • R 10 is hydrogen, Ci_ 4 alkyl, cyclopropyl, or trifluoromethyl; or R 10 is hydrogen, methyl, cyclopropyl, or trifluoromethyl; each R e independently is Ci_ 4 alkyl, cyclopropyl, Ci_ 4 alkoxy, or dimethylamino.
  • Ci_ 4 alkoxy is methoxy and Ci_ 4 alkyl is methyl.
  • R 4 is a group having the chemical structure:
  • Embodiments of the present invention are those compounds of formula I or any of the subgroups of compounds of formula I wherein R 11 is Ci_ 4 alkyl; or wherein R 11 is methyl.
  • One embodiment concerns the compounds 1 - 102 listed in Table I at the end of the experimental part, including the pharmaceutically acceptable salts and solvates thereof.
  • a particular embodiment concerns the free form (non pharmaceutically acceptable salts and solvates) of the compounds 1 - 102 listed in Table I.
  • said compounds being represented by formula I-a can be prepared by coupling an intermediate of formula II with a carboxylic acid derivative of formula III in an amide forming reaction.
  • the reaction conditions for this amide forming reaction are those used to couple amino acids in peptide synthesis.
  • Coupling agents that may be used can be selected from N-ethoxycarbonyl-2-ethoxy-l ,2-dihydroquinoline (EEDQ), N-iso- butoxycarbonyl-2-isobutoxy- 1 ,2-dihydroquinoline (IIDQ),
  • HATU (7-azabenzotriazol-l-yl)uronium hexafluorophosphate
  • BOP benzotriazole-l-yl- oxy-tris-(dimethylamino)-phosphonium hexafluorophosphate
  • PyBOP ® benzotriazol-l-yl- oxy-tris-pyrrolidino-phosphonium hexafluorophosphate
  • DCC dicyclohexyl- carbodiimide
  • EDCI 3-ethyl-l(N,N-dimethyl)aminopropylcarbodiimide
  • 1,3-diisopropylcarbodiimide 1,3-diisopropylcarbodiimide.
  • a catalyst may be added, for example 1 -hydro xy- benzotriazole (HOBt) or 4-dimethylaminopyridine (DMAP).
  • the reaction is usually conducted in the presence of a base, in particular an amine base such as a tertiary amine, e.g. triethylamine, N-methylmorpholine, N,N-diisopropylethylamine, (the latter also being referred to as or Hunig's base, DIPEA, or DIE A).
  • Solvents that can be used include bipolar aprotic solvents such as DMA, DMF or acetonitrile, halogenated hydrocarbons such as CH 2 CI 2 or CHCI 3 , ether solvents such as THF.
  • the coupling reaction is conducted with HATU using triethylamine as
  • formula I-b can be prepared by an urethane forming reaction of an intermediate of formula II with an appropriate electrophilic carbonyl compound of formula IV such as a chloro formate, or an activated 2,5-dioxopyrrolidin-l-olate, /?ara -nitropheno late or 2-pyridyl carbonate.
  • an appropriate electrophilic carbonyl compound of formula IV such as a chloro formate, or an activated 2,5-dioxopyrrolidin-l-olate, /?ara -nitropheno late or 2-pyridyl carbonate.
  • Lg in the above scheme is a leaving group such as chloro, bromo, 2,5-dioxopyrrolidin- l-olate, /?ara-nitrophenolate.
  • the intermediates of formula II in turn can be prepared as outlined in the following reaction scheme:
  • M represents a -B(OR a ) 2 group or a -Sn(R b ) 3 group, wherein R a represents a hydrogen or an alkyl or alkanediyl group, e.g. 2,3-dimethyl-2,3-butanediyl and R b represents an alkyl group such as methyl or butyl.
  • PG represents a hydroxy- protecting group that can be selectively cleaved in the presence of the Boc group.
  • Y represents bromo, iodo or a trifluoromethanesulfonyl (triflate or TfO-) group.
  • X represents chloro, bromo, or iodo.
  • the triflate group can be introduced by reacting an intermediate of formula X bearing a hydroxy group at the position of the bromo with a trifluoromethanesulfonimide, in the presence of a base in a solvent such as dichloromethane.
  • the intermediate of formula X bearing a hydroxy group in turn can be prepared from an intermediate XI bearing a protected hydroxy group at the position of the the group Y, following the procedures described hereinafter for the conversion of XI to X, followed by a deprotection step.
  • a protecting group that can be used in this procedure is a benzyl group, which can be removed with hydrogen in the presence of a catalyst.
  • the lactone XI is alkylated with a benzyl halide to the benzylated lactone X.
  • This reaction is conducted in an aprotic solvent such as THF, with a base, e.g.
  • the lactone in the intermediates X is ring-opened by hydrolysis using a base such as LiOH, NaOH, or KOH in an aqueous solvent such as a mixture of DMF, DMA, dioxane, THF and water.
  • intermediates VI For example in case of a t-butyldimethylsilyl group use can be made of tetrabutyl- ammonium fluoride (TBAF) or HF in acetonitrile.
  • TBAF tetrabutyl- ammonium fluoride
  • HF acetonitrile
  • the intermediates VI which can be bromo, iodo or triflate (-OTf) derivatives, are then subjected to a carbon-carbon cross- coupling reaction such as a Suzuki, Stille, Heck, or Negishi reaction that is metal- catalysed (usually with Pd, Ni or Cu catalysts).
  • cross-coupling reaction is the Suzuki reaction, in which case VI is reacted with a substituted heteroaryl boronic acid or ester (e.g. pinacolatoboronate) in the presence of a palladium catalyst at elevated temperature
  • a base such as sodium bicarbonate, sodium carbonate, sodium hydroxide, potassium carbonate, cesium carbonate, potassium phosphate, etc.
  • a base such as sodium bicarbonate, sodium carbonate, sodium hydroxide, potassium carbonate, cesium carbonate, potassium phosphate, etc.
  • an inorganic base is difficult to dissolve in an organic solvent, it is used as an aqueous solution.
  • Another such cross- coupling reaction is the Stille reaction in which case VI is reacted with a substituted heteroaryl stannane at elevated temperature in the presence of a palladium catalyst.
  • a metal salt like lithium chloride, lithium bromide or lithium iodide can be used as an additive.
  • additional ligands e.g. tri-t-butylphospine, l,l '-bis(diphenylphospino)ferrocene, tri-o-tolyl- phospine or the like
  • Heck reaction is the reaction of an unsaturated halide (or triflate) with an alkene and a base and palladium catalyst to form a substituted alkene.
  • Suitable catalyst for this reaction is Pd(PPh 3 )4.
  • Suitable organic solvents for this type of reactions include tetrahydrofuran, 1,4-dioxane and 1,2-di- methoxyethane, aromatic solvents such as benzene or toluene, alcohol solvents such as methanol or ethanol, acetonitrile, dimethylformamide, or a mixture of these solvents.
  • a base that can be used is an alkali metal acetate such as potassium acetate.
  • Boc-deprotection can also be accomplished by treatment of intermediate V with trimethylsilyl iodide or a mixture of trimethylsilyl chloride and Nal in an appropriate solvent e.g. acetonitrile, CHC1 3 or CH 2 CI 2 .
  • the Boc-deprotection reactions preferably are conducted at room temperature.
  • the intermediates of formula XI can be prepared as in the following reaction scheme wherein Y is as specified above and PG is a N-protecting group such as a BOC-group.
  • the alcohol function in the 2-phenethyl alcohol XVII is oxidized to the corresponding acetaldehyde XVI using a weak oxidant such as sodium hypochlorite in the presence of 2,2,6, 6-tetramethylpiperidine-l-oxyl (or TEMPO), which is a selective oxidant generating aldehydes from primary alcohols.
  • a weak oxidant such as sodium hypochlorite
  • TEMPO 2,2,6, 6-tetramethylpiperidine-l-oxyl
  • the synthetic steps in the preparation of compounds according to formula II can be performed in another order.
  • the cross-coupling reaction can be carried out at various stages in the synthetic sequence in the above scheme, such as on intermediates VI, VII, VIII, IX and XI.
  • the cross coupling can be even performed at a later stage of the synthesis, for example at the end of the synthesis as illustrated in the following reaction scheme.
  • M is as specified above and the cross- coupling reaction conditions also are as described above.
  • Intermediates XVIII can be prepared following the procedures for the preparation of intermediates II, but without cro -coupling reaction, followed by a coupling reaction to introduce the R 3 -CO-group.
  • said compounds being represented by formula I-c can be prepared by an amide forming reaction between an intermediate of formula XIX and cyanocyclopropyl carboxylic acid XX as illustrated in the following reaction scheme.
  • the conditions for this reaction are as described above, e.g. in the transformation of II into I-a.
  • an intermediate II is coupled with N-protected t.butylglycine XXI, such as Boc-t.butylglycine, in an amide-forming reaction, following reaction conditions as described above in the transformation of II to I-a, yielding an intermediate XXII.
  • XXII N-protected t.butylglycine
  • the Boc protecting group in XXII can be removed under art-known conditions, as described hereinbefore to obtain the free amino intermediate XIX.
  • said compounds being represented by formula I-d can be prepared by an urethane forming reaction at the end of the synthesis as illustrated in the following reaction scheme, by condensation of an intermediate of formula XIX with an appropriate electrophilic carbonyl compound such as a chloroformate, or an activated succinimidyl, para-nitrophenyl, or pyridyl carbonate.
  • This reaction is particularly suited for preparing
  • the compounds of formula I wherein R 3 is a group of formula: said compounds being represented by formula I-e can be prepared either by a coupling reaction with pyrrolidinyl acetic acid in an amide- forming reaction, following reaction conditions as described above.
  • the compounds I-e can also be prepared by a two-step procedure involving first the reaction of an intermediate XIX with chloroacetyl chloride in the presence of a base, e.g. a tertiary amine such as triethylamine, in a solvent such as dichloromethane, resulting in intermediates XXIII.
  • a base e.g. a tertiary amine such as triethylamine
  • This reaction can e.g.
  • the intermediates XXIII are then reacted with pyrrolidine in the presence of a nucleophilic catalyst such as tetrabutylammonium iodide or the like, preferentially in a bipolar aprotic solvent (e.g. DMA, DMF, N-methylpyrrolidinone). This reaction preferably is conducted at room temperature.
  • a nucleophilic catalyst such as tetrabutylammonium iodide or the like
  • a bipolar aprotic solvent e.g. DMA, DMF, N-methylpyrrolidinone
  • the compounds of formula I wherein R 2 is 3 -hydroxy chromanyl can also be prepared by first coupling a 3-hydroxy-4-chromanamine XXIV with a 3-arylpropionic acid XXV resulting in an intermediate XXVI, using conditions as described hereinbefore for the formation of an amide bond. Subsequently the NH and OH functions are protected with 2-methoxypropene resulting in intermediates XXVII. This transformation can be effected using a halogenated solvent, such as dichloromethane, in the presence of an acid catalyst, such as pyridinium /?-toluenesulfonate, between 0 C and room
  • the compounds of formula I can also be converted into each o nal group
  • the intermediates of formula R 2 -NH 2 wherein R 2 is a chromanol group can be prepared from a phenol XXXIII in 5 synthetic steps.
  • phenol XXXIII is treated with 3-bromopropionic acid, in water in the presence of a base such as NaOH, at elevated temperature, such as reflux temperature.
  • the resulting 3-phenoxypropionic acid XXXIV undergoes a Friedel Crafts acylation, using oxalyl chloride and A1C1 3 in a solvent such as dichloromethane to afford the chromanone XXXV, which in turn is brominated (with bromine or CuBr 2 ) in a halogenated solvent, such as dichloro methane to afford the bromo chromanone XXXVI.
  • Reduction with a metal hydride reagent, such as NaBH 4 in a protic solvent, such as methanol between 0°C and room temperature affords the bromo alcohol XXXVII.
  • the bromo alcohol XXXVII undergoes a Ritter reaction, using acetonitrile and an aqueous solution of a strong acid, such as sulfuric acid, to afford the intermediate oxazoline XXXVIII, that is hydro lyzed in diluted acid at a temperature between 80°C and 120°C to afford the racemic 4-amino chromanol of the formula XXXIX.
  • a strong acid such as sulfuric acid
  • 4-Amino-chromanol XXXIX can be halogenated at the 6- or 8-position, e.g. with N-chlorosuccinimide, to afford the corresponding 6- or 8-halo substituted 4-amino- chromanols.
  • the intermediates of formula R 2 -NH 2 which are be prepared from
  • Cyclohexanol amine of the formula XLIVIII can be prepared in 4 steps from
  • the acetate XLVa is obtained by treatment in isopropenyl acetate at 100°C in the presence of an acid catalyst, such as / ⁇ -toluene sulfonic acid.
  • the corresponding nitro ketone XL VI is obtained by reaction in a mixture of acetic anhydride and concentrated nitric acid at a temperature between room temperature and 50°C.
  • the keto function is reduced by a metal hydride reagent, such as sodium borohydride, in an alcoholic solvent, such as methanol at room temperature, to afford the nitro alcohol XL VII.
  • Reduction to the amino alcohol XL VIII is achieved by hydro geno lysis in the presence of Raney nickel in ethyl acetate.
  • the compounds of formula I and most of the intermediates in the present invention contain an asymmetric carbon atoms.
  • Pure stereo chemically isomeric forms of said compounds and said intermediates can be obtained by the application of art-known procedures.
  • diastereoisomers can be separated by physical methods such as selective crystallization or chromatographic techniques, e.g. counter current distribution, liquid chromatography and the like methods.
  • Enantiomers can be obtained from racemic mixtures by first converting said racemic mixtures with suitable resolving agents such as, for example, chiral acids, to mixtures of diastereomeric salts or compounds; then physically separating said mixtures of diastereomeric salts or compounds by, for example, selective crystallization or chromatographic techniques, e.g.
  • the compounds of formula I show anti-HIV properties, in particular they behave as HIV protease inhibitors.
  • HIV is the aetiological agent of Acquired Immune Deficiency Syndrome (AIDS) in humans and preferentially infects human T-4 cells and destroys them or changes their normal function, particularly the coordination of the immune system.
  • AIDS Acquired Immune Deficiency Syndrome
  • an infected patient has an ever-decreasing number of T-4 cells, which moreover behave abnormally.
  • the immunological defence system is unable to combat infections and neoplasms and the HIV infected subject usually dies by opportunistic infections such as pneumonia, or by cancers.
  • the compounds of the invention also show activity against drug- and multidrug- resistant HIV strains, in particular against HIV strains that have acquired resistance to one or more of the approved protease inhibitors, in particular to atazanavir, lopinavir, and ritonavir.
  • the compounds of formula I are useful in the treatment of individuals infected by HIV and for the prophylaxis of these infections.
  • Conditions that may be prevented or treated with the compounds of the present invention, especially conditions associated with HIV, include AIDS, AIDS-related complex (ARC), progressive generalized lymphadenopathy (PGL), as well as chronic Central Nervous System diseases caused by retroviruses, such as, for example HIV mediated dementia and multiple sclerosis.
  • the compounds of the present invention may therefore be used as a medicine against any of the above-mentioned conditions.
  • the compounds of formula I may be used in the manufacture of a medicament for the treatment or the prevention of HIV infection.
  • this invention provides a method of treating a human, suffering from, or a method of preventing humans to suffer from viral infections, especially HIV infections.
  • Said method comprises the administration, of an effective amount of a compound of formula I, a pharmaceutically acceptable addition salt, a pharmaceutically acceptable solvate thereof, or a possible stereoisomeric form thereof, to humans.
  • Said use as a medicine or method of treatment comprises the administration to HIV-infected subjects of an amount effective to combat the conditions associated with HIV and other pathogenic retroviruses, especially HIV-1.
  • compositions for treating HIV infection comprising a therapeutically effective amount of a compound of formula I and a pharmaceutically acceptable carrier or diluent.
  • compositions of the present invention may be formulated into various pharmaceutical forms for administration purposes.
  • compositions there may be cited all compositions usually employed for systemically administering drugs.
  • an effective amount of the particular compound, optionally in addition salt form, as the active ingredient is combined in intimate admixture with a pharmaceutically acceptable carrier, which carrier may take a wide variety of forms depending on the form of preparation desired for administration.
  • a pharmaceutically acceptable carrier which carrier may take a wide variety of forms depending on the form of preparation desired for administration.
  • These pharmaceutical compositions are desirably in unitary dosage form suitable, for example, for oral, rectal, or percutaneous administration.
  • any of the usual pharmaceutical media may be employed such as, for example, water, glycols, oils, alcohols and the like in the case of oral liquid preparations such as suspensions, syrups, elixirs, emulsions, and solutions; or solid carriers such as starches, sugars, kaolin, diluents, lubricants, binders, disintegrating agents and the like in the case of powders, pills, capsules, and tablets. Because of their ease in administration, tablets and capsules represent the most advantageous oral dosage unit forms, in which case solid pharmaceutical carriers are obviously employed. Also included are solid form preparations that can be converted, shortly before use, to liquid forms.
  • the carrier optionally comprises a penetration enhancing agent and/or a suitable wetting agent, optionally combined with suitable additives of any nature in minor proportions, which additives do not introduce a significant deleterious effect on the skin. Said additives may facilitate the administration to the skin and/or may be helpful for preparing the desired compositions.
  • These compositions may be administered in various ways, e.g., as a transdermal patch, as a spot-on, as an ointment.
  • the compounds of the present invention may also be administered via inhalation or insufflation by means of methods and formulations employed in the art for administration via this way.
  • the compounds of the present invention may be administered to the lungs in the form of a solution, a suspension or a dry powder.
  • Unit dosage form refers to physically discrete units suitable as unitary dosages, each unit containing a predetermined quantity of active ingredient calculated to produce the desired therapeutic effect in association with the required
  • unit dosage forms are tablets (including scored or coated tablets), capsules, pills, powder packets, wafers, suppositories, injectable solutions or suspensions and the like, and segregated multiples thereof.
  • an effective daily amount would be from 0.01 mg/kg to 50 mg/kg body weight, more preferably from 0.1 mg/kg to 10 mg/kg body weight. It may be appropriate to administer the required dose as two, three, four or more sub-doses at appropriate intervals throughout the day. Said sub-doses may be formulated as unit dosage forms, for example, containing 1 to 1000 mg, and in particular 5 to 200 mg of active ingredient per unit dosage form.
  • the exact dosage and frequency of administration depends on the particular compound of formula I used, the particular condition being treated, the severity of the condition being treated, the age, weight and general physical condition of the particular patient as well as other medication the individual may be taking, as is well known to those skilled in the art. Furthermore, it is evident that the effective amount may be lowered or increased depending on the response of the treated subject and/or depending on the evaluation of the physician prescribing the compounds of the instant invention. The effective amount ranges mentioned above are therefore only guidelines and are not intended to limit the scope or use of the invention to any extent.
  • the combination of one or more additional antiretroviral compounds and a compound of formula (I) can be used as a medicine.
  • the present invention also relates to a product containing (a) a compound of formula (I), and (b) one or more additional antiretroviral compounds, as a combined preparation for simultaneous, separate or sequential use in anti-HIV treatment.
  • the different drugs may be combined in separate preparations or in a single preparation, together with pharmaceutically acceptable carriers.
  • Said other antiretroviral compounds may be any known antiretroviral compounds such as nucleoside reverse transcriptase inhibitors (NRTIs), e.g.
  • NRTIs non-nucleoside reverse transcriptase inhibitors
  • tenofovir and its pro-drug tenofovir disoproxil fumarate TDF
  • protease inhibitors e.g. ritonavir (RTV), saquinavir (SQV), lopinavir (ABT-378, LPV), indinavir (IDV), amprenavir (VX-478), nelfmavir
  • Atazanavir BMS 232,632
  • darunavir TMC114
  • entry inhibitors which comprise fusion inhibitors (e.g. enfuvirtide (T-20) sifuvirtide, HRG-214, albuvirtide, SUC-HAS, and maC46/M87o), attachment inhibitors, modulators of intracellular cholesterol and corticosteroid biosynthesis (e.g. SP-01A), and co-receptor inhibitors, the latter comprise the CCR5 antagonists (e.g.
  • CXR4 antagonists e.g. AMD-070
  • entry inhibitors are TNX-355, INCB 9471, BMS-488043, nonakine, and VGV-1
  • maturation inhibitors e.g. bevirimat (PA-457) and becon
  • inhibitors of the viral integrase e.g. raltegravir (MK-0518), elvitegravir (JTK-303, GS-9137), BMS-538158, S-349572, JTK-656 S-247303, and GS-265744.
  • enantiomeric excess was determined by supercritical fluid chromatography (SFC) on a Chiralpak Daicel ® AD-H column.
  • SFC supercritical fluid chromatography
  • Compound names were generated using ChemDraw Ultra , version 9.0 (CambridgeSoft ® ).
  • Step 1 2,2,6,6-Tetramethylpiperidine-l-oxyl (TEMPO; 1.6 g, 1.0 mmol, 0.002 eq.) and NaBr (6 g, 500 mmol, 1.0 eq.) were successively added under vigorous stirring to a solution of alcohol 1-1 ([CAS No.: 4654-39-1]; 100 g, 500 mmol, 1.0 eq.) in dichloromethane (2300 mL) at 0°C. A solution of aqueous saturated NaHC0 3 and 10% NaOCl (400 mL) were added. The mixture was stirred for approximately ten minutes until thin- layer chromatography (TLC) indicated that the starting material had disappeared. The dichloromethane layer was separated.
  • TEMPO 2,2,6,6-Tetramethylpiperidine-l-oxyl
  • NaBr 6 g, 500 mmol, 1.0 eq.
  • the aqueous layer was rapidly extracted with diethyl ether.
  • the combined organic phases were washed with an aqueous solution of NaHS0 3 (10%) and KI (4%), brine, and dried with anhydrous sodium sulfate. After removing most of the volatiles under vacuum (keep temperature below 25°C), the resulting solution of aldehyde 1-2 in dichloromethane (50 mL) was used as such directly in the next step.
  • Step 2 A mixture of the dichloromethane solution of aldehyde 1-2 (460 mmol, 1.0 eq.), tert-butyl carbamate (107.8 g, 920 mmol, 2.0 eq.), sodium benzene sulfmate (151.0 g, 920 mmol, 2.0 eq.) and formic acid (42.3 g, 920 mmol, 2.0 eq.) in a mixture of methanol (250 mL) and water (500 mL) was stirred at 40°C for 24 hours (reaction was monitored by TLC). The reaction mixture was cooled to room temperature. The resulting precipitate was filtered off, washed with water and diethyl ether, and dried under reduced pressure to afford 150 g (72% starting from Intermediate 1-1) of Intermediate (rac)-l-3.
  • Step 3 To a mixture of diisopropylamine (26 g, 250 mmol, 1.1 eq.) in dry tetrahydrofuran (THF; 100 mL) was added dropwise n-butyllithium (100 mL of 2.5 M solution, 250 mmol, 1.1 eq.) at -78°C under nitrogen. The mixture was allowed to warm to room temperature and stirred at room temperature for 30 minutes. The mixture was re-cooled to -78°C and a solution of 2(5H)-furanone (21 g, 250 mmol, 1.1 eq.) in dry THF (100 mL) was added dropwise.
  • THF dry tetrahydrofuran
  • Step 1 Iodine (2.2 g, 8.0 mmol, 0.03 eq.) was added to a reaction flask charged with magnesium (79.8 g, 3282 mmol, 12.3 eq.) and THF (2.7 L) under nitrogen. The reaction mixture was heated to 30-35°C and maintained at this temperature. 4-Bromo- butene (361.4 g, 2677 mmol, 10.0 eq.) was slowly added over a period of two hours, the temperature of the reaction was kept below 65°C. After the addition was complete, the reaction mixture was stirred for a minimum of two hours at 60-65°C and then cooled in an ice bath.
  • Step 2 A solution of RuCl 3 .3H 2 0 (2.04 g, 7 mmol, 0.03 eq.) in water (77 mL) was added to a solution of NaI0 4 (236 g, 1105 mmol, 5.5 eq.) in water (1.9 L). This reaction mixture was added over 30 minutes to a solution of Intermediate 1-6 (107.7 g (wt% 71%), 201 mmol, 1.0 eq.) in acetone (1.9 L) at room temperature. The reaction mixture was stirred at room temperature until conversion was complete (approximately one hour). An aqueous Na 2 S 2 0 3 solution was added to the reaction mixture over 30 minutes.
  • Step 3 A mixture of Intermediate 1-7 (67.0 g (wt% 90%), 150 mmol, 1.0 eq.) and KHC0 3 (75.1 g, 750 mmol, 5.0 eq.) in dimethylformamide (DMF; 1200 mL) was stirred at room temperature for 20 minutes. Iodomethane (42.6 g, 300 mmol, 2.0 eq.) was added over a period of 20 minutes to the reaction mixture, the reaction mixture was stirred at room temperature for seven hours. After the reaction mixture was filtered over Celite, an aqueous solution of ammonium chloride was added at such a rate that the temperature stayed below 25°C. Next tert-butyl methyl ether was added and the mixture was filtered over Celite.
  • DMF dimethylformamide
  • Step 4 N-Selectride (135 mL of a 1M solution in THF, 135 mmol, 1.24 eq.) was dropwise added over a minimum of 1.5 hours to a solution of ester 1-8 (45 g,
  • Precursors 2, 14a, 15 and 17 were used as Precursors representing examples of formula R 2 -NH 2 as defined hereinbefore. Those for which no commercial supply is available can be synthesized according to literature procedures (Precursors 2, 14a, 15 and 17) or through procedures described in Examples 2 -13 (Precursors 3 - 14b).
  • R CI (+)-Precursor 10a
  • R CI (-)-Precursor 11a (-)-Precursor 12 (+)-Precursor 13
  • R Me (+)-Precursor 10b
  • R Me (+)-Precursor 11 b
  • Step 1 An ice-cooled solution of 3-bromopropionic acid (298 g, 1.95 mol, 1.25 eq.) and NaOH (156 g of an aqueous 50% solution, 1.95 mol, 1.25 eq.) in water (500 mL) was added over a period of 90 minutes to a mixture of 2-chlorophenol ([CAS No.: 95-57-8]; 200 g, 1.56 mol, 1.0 eq.) and NaOH (124 g of an aqueous 50% solution, 1.56 mol, 1.0 eq.) in water (1 L) at reflux temperature. The reaction mixture was stirred at reflux temperature for three hours.
  • 2-chlorophenol [CAS No.: 95-57-8]; 200 g, 1.56 mol, 1.0 eq.
  • NaOH 124 g of an aqueous 50% solution, 1.56 mol, 1.0 eq.
  • Step 2 A solution of acid 2-2 (112 g, 558 mmol, 1.0 eq.) and some drops of DMF in dichloromethane (1.5 L) was cooled in an ice bath. Oxalylchloride (142 g, 1.12 mol, 2.0 eq.) was added dropwise, the reaction mixture was allowed to warm to room temperature and stirred overnight. The solvent was concentrated under reduced pressure. The residue was reconstituted in dichloromethane (1.5 L). Aluminium trichloride (89 g, 670 mmol, 1.2 eq.) was added portion wise and the reaction mixture was stirred overnight at room temperature. The reaction mixture was slowly poured into a cooled 1 M hydrochloric acid solution.
  • Step 3 Bromine (30.7 mL, 598 mmol, 1.05 eq.) was slowly added to a solution of crude Intermediate 2-3 (104 g) in dichloromethane at reflux temperature. After the addition was complete, the resulting mixture was stirred at reflux temperature for 30 minutes. The reaction mixture was cooled to room temperature, washed with a saturated aqueous sodium metabisulfite solution and brine, dried with anhydrous MgS0 4 , and concentrated under vacuum to give a mixture of dibromine 2-4 and monobromine 2-5. The residue was dissolved in acetic acid (750 mL), and sodium sulfite (93 g, 740 mmol) was added. The reaction mixture was stirred at 70°C for three hours. The reaction mixture was cooled to room temperature and partially evaporated, water and dichloromethane were added. The organic layer was separated and concentrated under reduced pressure. Crude Intermediate 2-5 was used as such in the next step (no yield was determined).
  • Step 4 NaBH 4 (21.7 g, 574 mmol) was added in portions to a solution of crude Intermediate 2-5 in methanol (1.5 L) at 0°C and the mixture was stirred at room temperature for 30 minutes. The reaction mixture was partially concentrated under reduced pressure, and the residue was diluted with ethyl acetate. The organic phase was washed with brine, dried with anhydrous magnesium sulphate and concentrated under reduced pressure. The crude product was purified by silica gel column chromatography (eluent: dichloromethane dichloromethane / methanol 96:4) to provide 105.5 g (67% starting from Intermediate 2-3) of Intermediate 2-6.
  • Step 5 Concentrated sulfuric acid (16 mL, 300 mmol, 2.0 eq.) was dropwise added to a solution of Intermediate 2-6 (39.5 g, 150 mmol, 1.0 eq.) in acetonitrile (800 mL). The reaction was stirred at 45-50°C until no more starting material was present (about five hours) and then concentrated under reduced pressure. Water
  • Step 1 Di-tert-butyl dicarbonate (14.5 g, 66.6 mmol, 1.1 eq.) was dissolved in THF (100 mL), the solution was cooled to 0°C and stirred. (35',45)-4-Amino-chroman- 3-ol ((+)-Precursor 2) (10 g, 60.5 mmol, 1.0 eq.) and NaHC0 3 (5.1 g, 60.5 mmol, 1.0 eq.) were added simultaneously while maintaining good stirring. The reaction mixture was stirred at room temperature for four hours. The solvent was partially evaporated, water was added and the resulting mixture was extracted with diethylether. The combined organic extracts were washed with a 10% citric acid solution and brine, dried with MgSC ⁇ , filtered and evaporated to dryness to give 21 g of crude carbamate 4-1.
  • Step 2 The crude carbamate 4-1 was dissolved in DMF (100 mL) and
  • N-chlorosuccinimide (NCS; 8.9 g, 66.6 mmol, 1.1 eq.) was added. The reaction mixture was stirred at 80°C for one hour. The reaction mixture was cooled to room temperature, diluted with diethylether, washed with a saturated aqueous Na 2 C03 solution and brine, dried with anhydrous MgSC ⁇ and concentrated under reduced pressure to give 16.3 g (82%o over two steps) of crude Intermediate 4-2.
  • Step 3 A solution of 4-2 (16.3 g, 54.2 mmol, 1.0 eq.) and trifluoro acetic acid (TFA; 124 g, 1084 mmol, 20.0 eq.) in dichloromethane (100 mL) was stirred at room temperature for one hour. The reaction mixture was basified with a saturated Na 2 C0 3 solution and extracted with dichloromethane. The combined organic phases were washed with water and brine, and dried with MgSC ⁇ . The crude product was recrystallized form ethyl acetate to give 6.8 g (61%) of (-)-Precursor 5 (ee >95%).
  • TFA trifluoro acetic acid
  • (rac)-cz ' s-4-amino-8-fluorochroman-3-ol was prepared starting from commercially available 8-fluorochroman-4-one [CAS No.: 11141-00-5] using the procedures as exemplified for the preparation of (rac)-Precursor 3.
  • the racemic mixture was separated via preparative SFC on a Chiralpak Daicel ® AD-H column (30 x 250 mm, mobile phase: isocratic 32% methanol (containing 0.2% isopropylamine) / 68% C0 2 , flow rate: 50 mL/min), the desired (SS ⁇ -enantiomer ((+)-Precursor 6) was isolated as the first fraction (ee > 95%).
  • Example 8 Synthesis of (36 , ,4tS -4-amino-6,8-difluorochroman-3-ol ((+)-Precursor 9) (rac)-cz5-4-Amino-6,8-difluorocfiroman-3-ol was prepared starting from 2,4-difluoro- phenol [CAS No.: 367-27-1] using the procedures as exemplified for the preparation of (rac)-Precursor 3. The racemic mixture was separated via preparative SFC on a
  • (rac)-cz5-4-Amino-8-chloro-6-fluorochroman-3-ol was prepared starting from 2-chloro-4-fluorophenol [CAS No.: 1996-41-4] using the procedures as exemplified for the preparation of (rac)-Precursor 3.
  • the desired ((+)-Precursor 10a) was isolated via preparative SFC on Chiralpak Daicel ® AD-H column (30 x 250 mm, mobile phase: isocratic 40% methanol (containing 0.6% isopropylamine) / 60%) C0 2 , flow rate: 50 mL/min), the desired (35 * ,45)-enantiomer ((+)-Precursor 10a) was isolated as the first fraction (ee > 95%).
  • Step 1 To a solution of NaH (9.1 g of a 60%> dispersion in oil, 238 mmol, 1.2 eq.) in DMF (300 mL) at 0°C was drop wise added a solution of 2-methyl-4- f uorophenol [CAS No.: 452-72-2]; 25.0 g, 198 mmol, 1.0 eq.) in DMF (40 mL). The suspension was stirred at room temperature for 30 minutes and cooled again to 0°C, a solution of l-chloro-3-hydroxypropane (22.5 g, 238 mmol, 1.2 eq.) in DMF (40 mL) was added drop wise.
  • the reaction was heated for two hours at 60°C (an additional amount of NaH and l-chloro-3-hydroxypropane may be needed to complete the reaction).
  • the reaction mixture was cooled to room temperature and water was added, the water layer was extracted with diethyl ether, the combined organic phases were washed with an aqueous NaOH solution and brine, dried with anhydrous MgS0 4 and concentrated under reduced pressure.
  • the crude product was used as such in the next step.
  • Step 2 Intermediate 9b-2 (12.9 g, 70 mmol) was dissolved in a 1 :1 mixture of CH 3 CN / H 2 0 (425 mL).
  • TEMPO (1094 mg, 7 mmol, 0.1 eq.) and bis(acetoxy)- iodobenzene (BAIB; 56.4 g, 175 mmol, 2.5 eq.) were added portion wise and the reaction mixture was stirred at room temperature overnight (additional TEMPO and BAIB may be required to complete the oxidation).
  • Example 10a Synthesis of (36 , ,4tS -4-amino-6-chloro-8-fluorochroman-3-ol ((-)- Precursor 11a)
  • Example 11 Synthesis of (36 , ,4tS -4-amino-6-methylchroman-3-ol ((-)-Precursor 12) (rac)-czs-4-Amino-6-methylchroman-3-ol was prepared starting from 6-methyl- 4-chromanone [CAS No.: 39513-75-2] using the procedures as exemplified for the preparation of (rac)-Precursor 3.
  • (+)-Precursor 13 Step 1 A solution of 6,7-dihydro-5H-benzo[b]thiophen-4-one (starting material 12-1, [CAS No.: 13414-95-4]; 39 g, 256 mmol, 1.0 eq.) in THF (150 mL) was added dropwise to a mixture of sodium bis(trimethylsilyl)amide (NHMDS; 307 mL of a 1 M solution in THF, 307 mmol, 1.2 eq.) and THF (200 mL) at -78°C under argon atmosphere, the reaction mixture was stirred for an additional 30 minutes at -78°C.
  • starting material 12-1, [CAS No.: 13414-95-4] 39 g, 256 mmol, 1.0 eq.
  • Step 2 O-benzylhydroxylamine hydrochloride (41 g, 256 mmol, 1.0 eq.) was added to a solution of crude Intermediate 12-2 (50 g) in pyridine (500 mL). The reaction mixture was stirred at room temperature over weekend. The mixture was evaporated and co-evaporated two times with toluene. The residue was re-dissolved in ethyl acetate, the organic phase was washed with an aqueous 5% citric acid solution and brine, dried with anhydrous MgS0 4 and concentrated under reduced pressure to give 72 g of crude Intermediate 12-3.
  • Step 3 Borane dimethyl sulfide complex (198 mL of a 1 M solution in THF 395 mmol, 1.54 eq.) was added dropwise to a solution of crude Intermediate 12-3
  • Step 1 Ketone 13-1 ([CAS No. : 13368-65-5]; 430 g, 3.83 mol, 1.0 eq.) and /?ara-toluenesulfonic acid monohydrate (/?TSA.H 2 0; 72.9 g, 0.38 mol, 0.1 eq.) in isopropenyl acetate (2.5 L) were refluxed for 6 hours at 100°C. After the reaction mixture was cooled to room temperature, water was added.
  • Step 2 The isomeric mixture 13-2A and 13-2B (106.2 g, 0.95 mol, 1.0 eq.) was dissolved in acetic acid anhydride (400 mL). Concentrated nitric acid (61 mL,
  • Step 3 NaBH 4 (40 g, 1.03 mol, 1.3 eq.) was added in portions to a solution of Intermediate 13-3 (125 g, 795 mmol, 1.0 eq.) in dry methanol (3.0 L) at room temperature. The reaction mixture was stirred for 30 minutes at room temperature. The mixture was neutralized with an aqueous 10% KHS0 4 solution to pH ⁇ 7 and concentrated under reduced pressure. Water was added and the mixture was extracted with ethyl acetate. The combined organic phases were washed with brine, dried with anhydrous MgS0 4 and concentrated under reduced pressure to give a 1 : 1 mixture of Intermediate 13-4 and its epimeric alcohol.
  • Step 4 A solution of 13-4 (29 g, 169.6 mmol, 1.0 eq.) in ethyl acetate (1.25 L) was hydrogenated at atmospheric pressure for five hours at 5°C with Raney Ni (32 g) as catalyst. After uptake of hydrogen gas (3.0 eq.), the catalyst was filtered off. A hydrochloric acid solution in dioxane was added to the filtrate at 0°C, the resulting mixture was stirred for 30 minutes.
  • Precursor 18 Precursor 19 Precursor 20 Precursor 21
  • Precursor 22 Precursor 23 Precursor 24
  • Amine 14-1 was synthesized according to literature procedures starting from
  • Step 1 HATU (3.56 g, 9.35 mmol, 1.15 eq.) was added to a solution of amine 14-1 (1.8 g, 8.13 mmol, 1.0 eq.), 1-cyanocyclopropanecarboxylic acid (0.90 g,
  • Step 2 A solution of Intermediate 14-2 (1.83 g, 5.81 mmol, 1.0 eq.) in methanol was hydrogenated at atmospheric pressure at 25°C for 3 hours with Pd (Pd/C 10%) as catalyst. The reaction mixture was filtered over C elite and the filtrate concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluent: dichloromethane / methanol / acetic acid 97:2: 1) to give 0.75 g (58%) of
  • Precursors representing examples of formula R -M as defined hereinbefore which were used for Suzuki or Stille cross-coupling reactions. Those for which no commercial supply is available, can be synthesized according to literature procedures (Precursor 25 and 26) or by procedures described in Examples 15 and 16 (Precursors 27, 28, 36 and 37).
  • Precursor 25 Precursor 26 Precursor 27 Precursor 28 Precursor 29
  • Precursor 30 Precursor 31 Precursor 32 Precursor 33 Precursor 34
  • Precursor 35 Precursor 36 Precursor 37 Precursor 38 Precursor 39
  • Precursor 40 Precursor 41 Precursor 42 Precursor 43 Precursor 44
  • Precursor 27 Lithium diisopropylamide (LDA; 245 mL of a 2.5 M solution, 613.2 mmol, 1.2 eq.) was added over a period of two hours to a solution of 2-isopropylthiazole ([CAS No.: 15679-10-4]; 65 g, 511 mmol, 1.0 eq.) in dry THF (1.3 L) at -78°C. After stirring for one hour at this temperature, tributyltin chloride (111 mL, 408.8 mmol, 0.8 eq.) was added dropwise.
  • LDA 2-isopropylthiazole
  • tributyltin chloride 111 mL, 408.8 mmol, 0.8 eq.
  • Precursor 28 was synthesized analogously to Precursor 27 starting from 2- cyclopropylthiazole [CAS No.: 1159821-56-3], but using n-butyllithium as a base.
  • Example 16 Synthesis of 2-cyclopropyl-6-methyl-4-(4,4,5,5,-tetramethyl-l,3,2-dioxa- borolan-2-yl)-pyridine (Precursor 36)
  • Precursor 37 was synthesized analogously to Precursor 36 starting from 2,6-di- methylpyridine [CAS No.: 108-48-5].
  • Step 1 A solution of (-)-Precursor 1 (12.5 g, 32.5 mmol, 1.0 eq.) in dry THF (100 mL) was cooled to -78°C under nitrogen. Lithium bis(trimethylsilyl)amide (LHMDS; 68.3 mL of a 1 M solution in THF, 68.3 mmol, 2.1 eq.) was added slowly. After 30 minutes at -78°C, 2-fluorobenzyl bromide (4.19 mL, 34.2 mmol, 1.05 eq.) was added in one portion to the reaction mixture. Stirring was continued for 90 minutes at -78°C.
  • LHMDS Lithium bis(trimethylsilyl)amide
  • Step 2 NaOH (33.5 mL of a 1 M aqueous solution, 33.5 mmol, 5.0 eq.) was added to a solution of Intermediate 17-1 (3.3 g, 6.7 mmol, 1.0 eq.) in methanol (20 mL). The reaction mixture was stirred at room temperature for three hours. The reaction mixture was partially concentrated under reduced pressure and then acidified to pH ⁇ 2-3 with a 10% citric acid solution. The white precipitate was filtered off, washed with water and dried under high vacuum. Crude Intermediate 17-2 (3.33 g, 96%) was used as such in the next step.
  • Step 3 Imidazole (3.08 g, 45.2 mmol, 7.0 eq.) and tert-butyldimethylsilyl- chloride (4.87 g, 32.4 mmol, 5.0 eq.) were added to a solution of Intermediate 17-2 (3.33 g, 6.47 mmol, 1.0 eq) in DMF (650 mL). The reaction was stirred at room temperature overnight. Methanol (30 mL) was added and stirring was continued until liquid chromatography-mass spectrometry (LCMS) showed complete TBDMS- deprotection of the carboxylic acid. Ethyl acetate and a 10% citric acid solution were added to the reaction mixture.
  • LCMS liquid chromatography-mass spectrometry
  • Step 4 Triethylamine (0.89 g, 8.83 mmol, 1.2 eq.), HATU (2.94 g, 7.73 mmol, 1.05 eq.) and (+)-Precursor 2 (1.54 g, 7.73 mmol, 1.05 eq.) were successively added to a solution of Intermediate 17-3 (4.60 g, 7.36 mmol, 1.0 eq.) in DMF (70 mL). The reaction mixture was stirred for one hour at room temperature.
  • Tetrabutylammonium fluoride (TBAF, 73.64 mL of a 1 M solution in THF, 73.64 mmol, 10.0 eq.) was added and the reaction mixture was stirred at 50°C until complete TBDMS-deprotection.
  • Intermediate 17-4 was precipitated by the addition of a saturated aqueous Na 2 C0 3 solution to the reaction mixture. The precipitate was filtered off, washed with water and dried under high vacuum. The crude product was used as such in the next step.
  • Precursor 34 (303 mg, 1.83 mmol, 3.0 eq.), tetrakis(triphenylphospine)palladium (Pd(PPh 3 ) 4 ,; 141 mg, 0.12 mmol, 0.2 eq.) and Na 2 C0 3 (2.74 mL of a 2 M aqueous solution, 5.47 mmol, 9.0 eq.) in dioxane (3 mL) was stirred at 110°C for 30 minutes (to prevent the formation of side-products short reaction times were applied) under argon. The reaction mixture was then rapidly cooled in an ice bath and a saturated aqueous Na 2 C0 3 solution was added. The water layer was extracted with ethyl acetate, the combined organic phases were dried with anhydrous MgS0 4 and concentrated under reduced pressure. Crude Intermediate 17-5 was used as such in the next step.
  • Step 6 Crude Intermediate 17-5 was dissolved in a 5 to 6 M HC1 solution in isopropanol and stirred at room temperature until complete deprotection ( ⁇ 30 minutes, to prevent the formation of side-products the reaction time has to be kept as short as possible).
  • the reaction mixture was basified with a saturated aqueous Na 2 C0 3 solution and extracted with ethyl acetate.
  • the combined organic phases were washed with water, dried with anhydrous MgS0 4 and concentrated under reduced pressure to give crude Intermediate 17-6 which was used as such in the next step without purification.
  • Step 7 Triethylamine (246 mg, 2.43 mmol, 4.0 eq.) and HATU (266 mg, 0.69 mmol, 1.15 eq.) were successively added to a mixture of crude Intermediate 17-6 and Precursor 18 (132 mg, 0.69 mmol, 1.15 eq.) in DMF (8 mL). The reaction mixture was stirred for two hours at room temperature. Ethyl acetate was added, the organic phase was washed with a saturated Na 2 C0 3 solution and water, dried with anhydrous MgS0 4 and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluent: dichloromethane dichloromethane / methanol 97:3) to give 144 mg (31% starting from Intermediate 17-4) of Compound 7.
  • Compounds 99 and 100 were prepared analogously to Compound 7.
  • Compounds 8, 10, 13, 16, 26, and 27 were prepared analogously to Compound 7 but with Step 6 involving a TFA mediated Boc-deprotection step using the procedure as described for Step 2 in Example 27.
  • Compound 11 was prepared analogously to Compound 7, but using a Stille cross-coupling reaction as described in Example 23 and a TFA mediated Boc-deprotection step as described for Step 2 in Example 27.
  • Step 1 HATU (2.36 g, 6.22 mmol, 1.1 eq.) was added to a solution of
  • Step 2 A mixture of Intermediate 18-1 (4.33 g, 5.48 mmol, 1.0 eq.), Precursor 34 (1.82 g, 10.96 mmol, 2.0 eq.), Pd(PPh 3 ) 4 (0.63 g, 0.55 mmol, 0.1 eq.) and Na 2 C0 3 (30 mL of a 2 M aqueous solution, 60.3 mmol, 11.0 eq.) in dioxane (100 mL) was stirred at 100°C for 50 minutes (to prevent the formation of side-products the reaction time has to be kept as short as possible) under nitrogen. The reaction mixture was then rapidly cooled in an ice bath and a saturated aqueous Na 2 C0 3 solution was added.
  • Step 3 TBAF (10.9 mL of a 1 M solution in THF, 10.97 mmol, 2.0 eq.) was added to a solution of Intermediate 18-2 (4.56 g, 5.49 mmol, 1.0 eq.) in THF (30 mL). The reaction mixture was stirred at 50°C until complete deprotection. Water was added, the precipitate was filtered off, thoroughly washed with water and dried under high vacuum to give 3.77 g (86%) of Intermediate 18-3.
  • Compound 35 was prepared analogously to Compound 33.
  • Step 1 A solution of (-)-Precursor 1 (54.0 g, 131 mmol, 1.0 eq.) in dry THF (1000 mL) was cooled to -70°C under nitrogen. Lithium bis(trimethylsilyl)amide (306.8 mL of a 1 M solution in THF, 307 mmol, 2.35 eq.) was dropwise added over a period of one hour, after which the reaction mixture was stirred for an extra four hours. A solution of 2-fluorobenzyl iodide (34.0 g, 144 mmol, 1.1 eq.) in THF (100 mL) was added to the reaction mixture over one hour. Stirring was continued for 60 minutes at -70°C.
  • Step 2 LiOH (1.4 L of a 1 M aqueous solution, 1.4 mol, 5.0 eq.) was dropwise added to a solution of Intermediate 20-1 (140 g, 284 mmol, 1.0 eq.) in methanol (3.5 L) at room temperature. The reaction mixture was stirred at room temperature until no more starting material was left. The reaction mixture was concentrated under reduced pressure and filtered. The precipitate was filtered off, washed with water and dried under vacuum at 50°C to give 120 g (82%) of Intermediate 20-2.
  • Step 3 A 3 L reaction flask was charged with water and stirred at reflux temperature for 30 minutes under N 2 . After the water was cooled to 40°C, methanol (300 mL), Intermediate 20-2 (100 g, 194 mmol, 1.0 eq.), Na 2 C0 3 (83 g, 783 mmol, 4.0 eq.), Pd(OAc) 2 (661 mg, 2.9 mmol, 0.015 eq.) and Precursor 30 (60 g, 392 mmol, 2.0 eq.) were successively added. The reaction mixture was degassed with N 2 and heated to 75°C over 10 minutes. The reaction mixture was stirred at 75°C for 30 minutes and then cooled to room temperature.
  • Step 4 Intermediate 20-3 was converted to Intermediate 20-4 with 70% yield using the procedure as described for Step 3 in Example 17.
  • Step 5 Triethylamine (2.67 g, 38.7 mmol, 3.0 eq.) was dropwise added to mixture of Intermediate 20-4 (8.45 g, 12.9 mmol, 1.0 eq.), HATU (5.15 g, 13.6 mmol, 1.05 eq.) and (-)-Precursor 14 (2.25 g, 13.6 mmol, 1.05 eq.) in acetonitrile (20 mL). After the reaction mixture was stirred at room temperature for one hour the pH of the reaction solution was adjusted to 8-9 by the addition of an aqueous Na 2 C0 3 / NaHCC solution. Extraction was carried out with ethyl acetate, the combined organic phases were washed with water, dried with Na 2 S0 4 and concentrated under reduced pressure to afford 12.4 g (86%) of Intermediate 20-5.
  • Step 6 A mixture of Intermediate 20-5 (12.44 g, 16.3 mmol, 1.0 eq.) and Nal (15.86 g, 105.8 mmol, 6.5 eq.) in acetonitrile (130 mL) was stirred at 0 ⁇ 5°C. A solution of TMSC1 (9.76 g, 89.5 mmol, 5.5 eq.) in acetonitrile (20 mL) was dropwise added over a period of one hour. Stirring was continued until complete Boc-deprotection ( ⁇ 90 minutes).
  • Step 7 Intermediate 20-6 was converted to Compound 96 according to the procedure as described for Step 7 in Example 17.
  • Step 6 A mixture of Intermediate 20-7 (122 g, 152 mmol, 1.0 eq.) and Nal (149 g, 996 mmol, 6.5 eq.) in acetonitrile (1200 mL) was stirred at 0 ⁇ 5°C. A solution of TMSC1 (91.5 g, 842 mmol, 5.5 eq.) in acetonitrile (200 mL) was dropwise added over a period of one hour. Stirring was continued until complete Boc-deprotection ( ⁇ 30 minutes). TBAF (1600 mL of a 2 M solution in THF, 3.04 mol, 20.0 eq.) was dropwise added over five hours to the reaction mixture at 0 ⁇ 5°C.
  • Step 7 Triethylamine (26.4 g, 264 mmol, 2.0 eq.) was added to a mixture of HATU (52.2 g, 137 mmol, 1.05 eq.), Intermediate 20-8 (77 g, 131 mmol, 1.0 eq.) and Precursor 18 (25.9 g, 137 mmol, 1.05 eq.) in DMF (770 mL). The reaction mixture was stirred for one hour at room temperature. An aqueous Na 2 C0 3 solution and water were added, the mixture was stirred for 30 minutes. The precipitate was filtered off, washed with water and dried under vacuum at 50°C to give 83 g crude of Compound 93. After recrystallization in a water/ethanol mixture, 78 g (79%) of Compound 93 was obtained.
  • Step 1 Triethylamine (119 mg, 1.18 mmol, 1.2 eq.), HATU (412 mg, 1.09 mmol, 1.1 eq.) and (+)-Precursor 8 (199 mg, 1.18 mmol, 1.1 eq.) were successively added to a solution of Intermediate 21-1 (681 mg, 0.99 mmol, 1.0 eq.) in acetonitrile (10 mL). The reaction mixture was stirred for one hour at room temperature. Nal (961 mg, 6.41 mmol, 6.5 eq.) and TMSC1 (589 mg, 5.42 mmol, 5.5 eq.) were successively added to the reaction mixture, stirring was continued until complete Boc-deprotection ( ⁇ 2 hours).
  • Step 2 Triethylamine (91 mg, 0.90 mmol, 2.0 eq.) and HATU (179 mg, 0.47 mmol, 1.05 eq.) were successively added to a mixture of Intermediate 21-2
  • Step 3 A mixture of Intermediate 21-3 (165 mg, 0.203 mmol, 1.0 eq.),
  • Precursor 30 (62 mg, 0.406 mmol, 2.0 eq.), Pd(PPh 3 ) 4 (23 mg, 0.020 mmol, 0.1 eq.) and Na 2 C0 3 (0.91 mL of a 2 M aqueous solution, 1.83 mmol, 9.0 eq.) in dioxane (2 mL) was stirred at 110°C for 15 minutes under argon. The reaction mixture was then rapidly cooled in an ice bath and a saturated aqueous Na 2 C0 3 solution was added. The precipitate was filtered off, washed with water and dried under reduced pressure. The crude product was purified by silica gel column chromatography (eluent:
  • Intermediate 22-1 was prepared using the procedures as exemplified for the preparation of Intermediate 17-4.
  • Intermediate 22-1 was converted to Intermediate 22-2 using the Boc-deprotection procedure as described in Example 19.
  • the latter was converted to Compound 44 via intermediate 22-3 using respectively the procedures from Step 2 and Step 3 as described in Example 21.
  • Step 1 HATU (1.25 g, 3.30 mmol, 1.05 eq.) was added to a mixture of triethylamine (954 mg, 9.42 mmol, 3.0 eq.), (+)-Precursor 2 (519 mg, 3.14 mmol, 1.0 eq.) and Intermediate 25-1 (2.0 g, 3.14 mmol, 1.0 eq.) in DMF (10 mL). The reaction mixture was stirred for 30 minutes at room temperature. Ethyl acetate was added, the organic phase was washed with a saturated aqueous Na 2 C03 solution and brine, dried with MgSC ⁇ and concentrated under reduced pressure. The crude product was purified by silica gel column chromatography (eluent: dichloromethane
  • Step 2 A mixture of Intermediate 25-2 (1.67 g, 2.13 mmol, 1.0 eq.) and TBAF (32.0 mL of a 1 M solution in THF, 32.0 mmol, 15.0 eq.) in THF (40 mL) was stirred at room temperature overnight. Ethyl acetate and brine were added to the reaction mixture. The organic layer was separated, thoroughly washed with water and dried to give 1.47 g (100%)) of crude Intermediate 25-3. The crude product was used as such in the next step.
  • Step 3 Intermediate 25-3 was converted to Intermediate 25-4 involving a TFA mediated Boc-deprotection step using the procedure as described for Step 2 in Example 27. The latter was converted to Compound 17 using respectively the procedures from Step 2 and Step 3 as described in Example 21.
  • Step 2 Lactone 26-2 was converted to Intermediate 26-3 according to the procedure as described for Step 1 in Example 17. Purification by silica gel column chromatography (eluent: heptane heptane / ethyl acetate 5:5) gave Intermediate 26-3 with 73% yield.
  • Step 3 NaOH (124.5 mL of a 1 M aqueous solution, 124.5 mmol, 9.3 eq.) was added to a solution of Intermediate 26-3 (7.18 g, 13.5 mmol, 1.0 eq.) in THF (120 mL). The reaction mixture was stirred at room temperature for one hour. The reaction mixture was partially concentrated under reduced pressure and then acidified with an aqueous 10% citric acid solution until pH ⁇ 6. The water phase was extracted with dichloromethane, the combined organic phases were dried with anhydrous MgSC ⁇ and concentrated under reduced pressure to give 7.40 g (99%) of Intermediate 26-4.
  • Step 4 Intermediate 26-4 was converted to Intermediate 26-5 according to the procedure as described for Step 3 in Example 17. Purification by silica gel column chromatography (eluent: dichloromethane dichloromethane / methanol 96:4) gave Intermediate 26-5 with 84% yield.
  • Step 5 Intermediate 26-5 was converted to Intermediate 26-6 using the procedure as described for Step 1 in Example 21. The latter was converted to Compound 51 using the procedure as described for Step 7 in Example 17.
  • Step 1 Intermediate 26-5 was reacted with racemic (rac)-Precursor 4 using the procedure as described for Step 4 in Example 17.
  • the crude reaction product was suspended in a mixture of acetonitrile and methanol (1 : 1) at reflux temperature. After cooling down to 0°C, the precipitate was filtered off to give a 1 : 1 mixture of
  • Step 2 TFA (10 mL, 135 mmol, 129 eq.) was added to a 1 : 1 mixture of Intermediate 27-lA and Intermediate 27-lB (765 mg, 1.04 mmol, 1.0 eq.) in dichloro- methane (200 mL). The reaction mixture was stirred at room temperature until LCMS showed complete conversion (-30 minutes, to prevent the formation of side-products the reaction time has to be kept as short as possible). A saturated aqueous Na 2 C03 solution was added, the layers were separated, the water layer was extracted with dichloromethane. The combined organic phases were washed with brine, dried with anhydrous MgSC ⁇ and concentrated under reduced pressure. Both isomers were separated by silica gel column chromatography (eluent: dichloromethane
  • Step 1 Lactone 29-1 [CAS No.: 165453-05-4] was converted to Intermediate 29-2 with 62% yield using the procedure as described for Step 1 in Example 17.
  • Step 2 Intermediate 29-2 (290 mg, 558 mmol, 1.0 eq.) was dissolved in MeOH (15 mL) and hydrogenated in a H-Cube with 10% Pd/C as a catalyst cartridge.
  • Step 3 Intermediate 29-3 (1.38 g, 3.36 mmol, 1.0 eq.) was dissolved in dry dichloromethane. N-Phenyl-bis-(trifluoromethanesulfonimide) (1.44 g, 4.03 mmol, 1.2 eq.) and CS 2 CO 3 (1.31 g, 4.03 mmol, 1.2 eq.) were added and the resulting suspension was stirred at room temperature for 16 hours until complete conversion according LCMS analysis. The mixture was diluted with dichloromethane and washed with an aqueous NaHC0 3 solution and brine. The organic phase was dried with Na 2 S0 4 and concentrated under reduced pressure. The crude product was purified by silica gel column chromatography (eluent: isohexane / ethyl acetate) to give 1.74 g (92%) of Intermediate 29-4.
  • Step 4 Intermediate 29-4 (1.55 g, 2.78 mmol, 1.0 eq.) was dissolved in THF (25 mL) followed by the addition of LiOH (5 mL of a 1 M aqueous solution, 5.0 mmol, 1.8 eq.) and MeOH (10 mL). The reaction was left stirring at room temperature for 1 hour. Solvents were co-evaporated with toluene and dried in vacuo. The residue and imidazole (3.79 g, 55.6 mmol, 20.0 eq.) were dissolved in dry DMF (10 mL).
  • Step 5 DIPEA (1.5 mL, 8.65 mmol, 4.0 eq.) was added to a stirred solution of Intermediate 29-5 (1.5 g, 2.16 mmol, 1.0 eq.), (-)-Precursor 16 (437 mg, 3.03 mmol, 1.4 eq.) and (benzotriazol-l-yloxy)tripyrrolidinophosphonium hexafluorophosphate (PyBOP, 1.35 g, 2.59 mmol) in dry DMF (15 mL). After two hours the mixture was diluted with dichloromethane (50 mL) and washed with aqueous NaHC0 3 , dried and concentrated to dryness to give crude Intermediate 29-6 which was used as such in the next step.
  • DIPEA 1.5 mL, 8.65 mmol, 4.0 eq.
  • Step 6 A suspension of crude Intermediate 29-6, the HC1 salt of Precursor 34 (109 mg, 0.55 mmol), Pd(PPh 3 ) 2 Cl 2 (35 mg, 0.055 mmol) and DIPEA (288 mg,
  • Step 7 HC1 (1.25 mL of a 4 M solution in dioxane) was added to a solution of Intermediate 29-7 (180 mg, 0.23 mmol, 1.0 eq.) in dioxane (5 mL) and methanol (1 mL). After 40 minutes stirring at room temperature, the mixture was concentrated to dryness and the residue dried under vacuum. The residue was redissolved in DMF (10 mL), Precursor 18 (51 mg, 0.27 mmol, 1.2 eq.), PyBOP (142 mg, 0.27 mmol, 1.2 eq.) and DIPEA (121 mg, 0.94 mmol, 4.0 eq.) were added. The reaction mixture was stirred for four hours at room temperature.
  • Step 1 Intermediate 29-4 (430 mg, 0.765 mmol) dissolved in N,N-dimethyl- acetamide (DMA; 11 mL) was loaded in a microwave vial together with 2-ethylthiazole ([CAS No.: 15679-09-1]; 433 mg, 3.83 mmol, 5.0 eq.), KOAc (113 mg, 1.17 mmol, 1.5 eq.) and Pd(PPh 3 ) 4 (44 mg, 38.3 ⁇ , 0.05 eq.). The reaction mixture was degassed with N 2 and then heated in a microwave at 150°C for one hour.
  • DMA N,N-dimethyl- acetamide
  • Step 2 HC1 (10 mL of a 4 M solution in dioxane) was added to Intermediate 30-1 (169 mg, 0.323 mmol, 1.0 eq.), the mixture was stirred at room temperature for one hour. The reaction mixture was freeze dried over night. The residue was redissolved in dichloromethane (10 mL), followed by the addition of Precursor 18 (67 mg, 0.355 mmol, 1.1 eq.) and DIPEA (281 ⁇ ,, 1.62 mmol, 5.0 eq.). The reaction mixture was cooled to 0°C, HATU (129 mg, 0.339 mmol, 1.05 eq.) was added and stirring was continued at room temperature for three hours. The reaction mixture was washed with 1 M HC1, a saturated aqueous NaHC0 3 solution and brine. The organic phase was dried with Na 2 S0 4 and concentrated under reduced pressure to give 185 mg (96%) of Intermediate 30-2.
  • Step 3 Intermediate 30-2 was converted to Intermediate 30-3 according to the procedure as described for Step 4 in Example 29 (49% yield).
  • Step 4 HATU (74 mg, 194 ⁇ , 1.1 eq.) was added to a solution of
  • Step 5 A solution of Intermediate 30-4 (35 mg, 41 ⁇ , 1.0 eq.) in CH 3 CN (3 mL) was cooled to 0°C. HF (170 ⁇ ) was dropwise added and stirring was continued at room temperature for two hours. The reaction was quenched by careful addition of a saturated aqueous NaHC0 3 solution, followed by ethyl acetate. Both phases were separated, the organic phase was washed with saturated aqueous NaHC0 3 , dried with anhydrous Na 2 S0 4 and evaporated under reduced pressure. The residue was purified by reversed phase preparative HPLC affording 10 mg (31%) of Compound 84.
  • Step 1 Intermediate 29-4 was reacted with Precursor 34 according to the procedure as described for Step 6 in Example 29.
  • Step 2 Intermediate 31-1 was converted to Intermediate 31-2 using the procedure as exemplified for Step 4 in Example 29.
  • Step 3 Intermediate 31-2 was reacted with (-)-Precursor 15 to give
  • Step 1 (+)-Precursor 2 (10.0 g, 60.5 mmol, 1.0 eq.) was added to a mixture of 3-(3-chlorophenyl)propanoic acid (11.2 g, 60.5 mmol, 1.0 eq.), triethylamine (12.3 g, 121 mmol, 2.0 eq.) and HATU (10.0 g, 60.5 mmol, 1.0 eq.) in DMF (120 mL) at -10°C. The reaction mixture was stirred at 0°C for two hours. Ethyl acetate and water were added.
  • Step 2 2-Methoxypropene (34.3 g, 476 mmol, 10.0 eq.) was dropwise added over a period of 30 minutes to a solution of intermediate 32-1 (15.8 g, 47.6 mmol, 1.0 eq.) and pyridinium /?-toluenesulfonate (PPTS, 1.2 g, 4.8 mmol, 0.1 eq.) in dichloromethane at 0°C. The reaction mixture was stirred at room temperature for 24 hours. Ethyl acetate and water were added. The organic layer was separated, washed with water, a 1 M HCl solution and a saturated aqueous Na 2 C03 solution, dried with MgS04 and concentrated under reduced pressure.
  • PPTS pyridinium /?-toluenesulfonate
  • Step 3 n-Butyllithium (17.4 mL of a 2.5 M solution in hexane, 43.6 mmol, 2.05 eq.) was dropwise added to a solution of Intermediate 32-2 (7.9 g, 21.2 mmol, 1.0 eq.) and epoxide 32-3 ([CAS No.: 1003871-37-1]; 7.2 g, 21.2 mmol, 1.0 eq.) in THF (200 mL) at -78°C.
  • Amine 35-1 was prepared using the procedures as exemplified for the preparation of Intermediate 28-3.
  • a solution of Intermediate 35-1 (250 mg, 0.39 mmol, 1.0 eq.) and Precursor 24 (150 mg, 0.55 mmol, 1.4 eq.) in DMF (4 mL) was stirred for one hour at room temperature.
  • Water and a saturated aqueous Na 2 C0 3 solution were added to the reaction mixture, the precipitate was filtered off and washed with water.
  • the crude product was suspended in boiling acetonitrile and subsequently allowed to cool to room temperature, 236 mg (73%) of Compound 79 was obtained as a white powder.
  • Compound 81 was prepared analogously to Compound 79.
  • Compound 68 was prepared analogously to Compound 79, but starting from amine 18-4.
  • Amine 36-1 was prepared using the procedures as exemplified for the preparation of Intermediate 26-6.
  • Step 1 Amine 36-1 (164 mg, 0.26 mmol, 1.0 eq.) and Precursor 19 (67 mg, 0.29 mmol, 1.1 eq.) were dissolved in acetonitrile (15 mL). Triethylamine (55 ⁇ , 0.40 mmol, 1.5 eq.) and HATU (111 mg, 0.29 mmol, 1.1 eq.) were successively added. The reaction mixture was stirred for 30 minutes at room temperature. Nal (436 mg, 2.91 mmol, 11.0 eq.) and TMSC1 (287 mg, 2.65 mmol, 10.0 eq.) were added and stirring was continued for one hour.
  • Step 2 A solution of Intermediate 36-2 (149 mg, 0.20 mmol, 1.0 eq.),
  • Precursor 23 (66 mg, 0.31 mmol, 1.5 eq.) and triethylamine (41 mg, 0.41 mmol, 2.0 eq.) in DMF (15 mL) was stirred at room temperature for one hour. Water and a saturated aqueous Na 2 C0 3 solution were added to the reaction mixture, the precipitate was filtered off and washed with water. After purification by silica gel column chromatography (eluent: dichloromethane dichloromethane / methanol 96:4) 62 mg (36%) of Compound 57 was obtained.
  • Compound 55 was prepared analogously to Compound 57.
  • Compound 34 was prepared analogously to Compound 57 but starting from amine 18-4.
  • Step 1 Intermediate 37-1 was converted to Intermediate 37-2 using the procedure as described for Step 1 in Example 36.
  • Step 2 A solution of Intermediate 37-2 (287 mg, 0.43 mmol, 1.0 eq.) in dichloromethane (4 mL) was slowly added to a mixture of chloroacetyl chloride (73 mg, 0.65 mmol, 1.5 eq.) and triethylamine (0.18 mL, 1.30 mmol, 3.0 eq.) in dichloromethane (4 mL) at 0°C. The reaction mixture was stirred at room temperature until complete conversion and then washed with a saturated aqueous NH 4 C1 solution, dried with anhydrous MgS0 4 and concentrated under reduced pressure to give 240 mg (77%) of crude Intermediate 37-3.
  • Step 3 A mixture of Intermediate 37-3 (240 mg, 0.33 mmol, 1.0 eq.), pyrrolidine (0.286 mL, 3.25 mmol, 10 eq.) and tetrabutylammonium iodide (TBAI; 12 mg, 0.03 mmol, 0.1 eq.) in N-methylpyrrolidinone (NMP; 3 mL) was stirred at room temperature until complete conversion. Water was added to the reaction mixture, the precipitate was filtered off, washed with water and dried under high vacuum. The crude product was purified by silica gel column chromatography (eluent: dichloromethane dichloromethane / methanol 95:5) to give 216 mg (85%) of Compound 97.
  • Example 38 Synthesis of Compound 9
  • Step 1 Intermediate 38-1 (610 mg, 0.96 mmol, 1.0 eq.) and Precursor 19
  • Step 2 Intermediate 38-2 was converted to Intermediate 38-3 according to the TFA mediated Boc-deprotection procedure as described for Step 2 in Example 27.
  • Step 3 DIPEA (74 mg, 0.57 mmol, 3.0 eq.) and HATU (76 mg, 0.20 mmol, 1.05 eq.) were successively added to a solution of Intermediate 38-3 (142 mg, 0.19 mmol, 1.0 eq.) and Precursor 20 (25 mg, 0.19 mmol, 1.0 eq.) in DMF (3 mL). The reaction mixture was stirred for 30 minutes at room temperature. A saturated aqueous Na 2 C0 3 solution was added, the water phase was extracted with ethyl acetate. The combined organic phases were washed with brine and concentrated under reduced pressure. The crude product was purified by preparative HPLC to give 45 mg (26% over two steps) of Compound 9.
  • Amine 39-1 was prepared starting from Intermediate 18-4 using the procedure as described for Step 1 in Example 36.
  • Intermediate 39-1 210 mg, 0.29 mmol, 1.0 eq.
  • Precursor 21 32 mg, 0.29 mmol, 1.0 eq.
  • DMF 10 mL
  • Triethylamine 58 mg, 0.58 mmol, 2.0 eq.
  • HATU 115 mg, 0.30 mmol, 1.05 eq.
  • Retention time (R t ) are given in minutes and were determined via Reversed phase UPLC (Ultra Performance Liquid Chromatography) on a BEH C18 column (1.7 ⁇ , 2.1 x 50 mm, Waters Acquity) with a flow rate of 0.7 ml/min and column temperature of 70°C.
  • Two mobile phases (mobile phase A: MeOH; mobile phase B: 10 mM NH 4 OAc in 90% H 2 0 and 10%> CH3CN) were used to run a gradient condition starting from 5% A and 95% B to 95% A and 5% B in 1.3 minutes, hold for 0.2 minutes, then back to 5% A and 95% B in 0.2 minutes and finally hold these conditions for
  • Melting points (m.p.) were determined with a DSC1 STAR 6 (Mettler-Toledo). Melting points were measured with a temperature gradient of 10°C/min. The starting temperature was 30°C, the maximum temperature 300°C. Values are peak values.
  • MT4-LTR-EGFP cells were obtained by transfecting MT4 cells with a selectable construct encompassing the sequences coding for the HIV long terminal repeat (LTR) as a promoter for the expression of enhanced green fluorescent protein (EGFP) and subsequent selection of permanently transfected cells.
  • LTR HIV long terminal repeat
  • EGFP enhanced green fluorescent protein
  • the antiviral activity on different HIV-1 strains was determined in a cell-based virus replication assay.
  • MT4-LTR-EGFP cells (150,000 cells/ml) are infected
  • toxicity of inhibitors is determined in parallel on mock-infected MT4 cells (150,000 cells/ml) stably transformed with a CMV-EGFP reporter gene and cultured in the presence or absence of test compound concentrations.
  • Two methodologies for readout were used, either quantification of GFP-fluoresence on day 3, or quantification of cell- viability using rezazurin on day 4. Both methods showed similar dose-respons curves from which CC50s could be determined. 50% HS- Rezazurin
  • FCS fetal calf serum
  • Strains A, B, and C are clinical isolates that include the following protease inhibitor resistance mutations in the protease domain (background mutations are not mentioned).
  • LPV lopinavir
  • ATV atazanavir

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  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)

Abstract

L'invention concerne des inhibiteurs de VIH de formule (I), où R1 représente un halogène, un alcoxy en C1 à C4, un trifluorométhoxy; n est 0 ou 1; A est CH ou N; R5 et R6 représentent un hydrogène, un alkyle en C1 à C4, un halogène; R7 et R8 représentent un alkyle en C1 à C4 ou un (alcoxy en C1 à C4)-alkyle en C1 à C4; R9 représente un alkyle en C1 à C4, un cyclopropyle, un trifluorométhyle, un alcoxy en C1 à C4 ou un diméthylamino; R10 représente un hydrogène, un alkyle en C1 à C4, un cyclopropyle, un trifluorométhyle, un alcoxy en C1 à C4 ou un diméthylamino; leurs sels d'addition à un acide et solvates pharmaceutiquement acceptables; des compositions pharmaceutiques contenant ces composés en tant que principe actif et des procédés de préparation de ces composés.
PCT/EP2010/069328 2009-12-11 2010-12-10 5-amino-4-hydroxypentoylamides WO2011070131A1 (fr)

Priority Applications (19)

Application Number Priority Date Filing Date Title
UAA201205119A UA108744C2 (xx) 2009-12-11 2010-10-12 5-аміно-4-гідроксипентоїламіди
AP2012006228A AP3217A (en) 2009-12-11 2010-12-10 5-Amino-4-hydroxypentoyl amides
JP2012542555A JP5797662B2 (ja) 2009-12-11 2010-12-10 ５−アミノ−４−ヒドロキシペントイルアミド
DK10790938.4T DK2509950T3 (en) 2009-12-11 2010-12-10 5-amino-4-hydroxypentoylamides
NZ599916A NZ599916A (en) 2009-12-11 2010-12-10 5-amino-4-hydroxypentoyl amides
ES10790938.4T ES2536774T3 (es) 2009-12-11 2010-12-10 5-Amino-4-hidroxipentoilamidas
CN201080055694.9A CN102770413B (zh) 2009-12-11 2010-12-10 5-氨基-4-羟基-戊酰基酰胺
EP10790938.4A EP2509950B1 (fr) 2009-12-11 2010-12-10 5-Amino-4-hydroxypentoyl amides
KR1020127017093A KR101771698B1 (ko) 2009-12-11 2010-12-10 5-아미노-4-하이드록시펜토일 아미드
EA201290487A EA020758B1 (ru) 2009-12-11 2010-12-10 5-амино-4-гидроксипентоиламиды
BR112012013493-0A BR112012013493B1 (pt) 2009-12-11 2010-12-10 amidas de 5-amino-4-hidróxi-pentoíla e composição farmacêutica que as compreende
PL10790938T PL2509950T3 (pl) 2009-12-11 2010-12-10 5-Amino-4-hydroksypentoilo-amidy
MX2012006613A MX2012006613A (es) 2009-12-11 2010-12-10 5-amino-4-hidroxipentoilamidas.
US13/515,187 US8592429B2 (en) 2009-12-11 2010-12-10 5-amino-4-hydroxypentoyl amides
CA2783929A CA2783929C (fr) 2009-12-11 2010-12-10 5-amino-4-hydroxypentoylamides
AU2010329867A AU2010329867B2 (en) 2009-12-11 2010-12-10 5-amino- 4-hydroxypentoyl amides
SG2012042552A SG181609A1 (en) 2009-12-11 2010-12-10 5-amino- 4-hydroxypentoyl amides
IL219272A IL219272A (en) 2009-12-11 2012-04-19 5-Amino-4-Hydroxypentoyl amide
HK13104373.4A HK1177454A1 (en) 2009-12-11 2013-04-10 5-amino- 4-hydroxypentoyl amides 5--4--

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
EP09178979.2 2009-12-11
EP09178979 2009-12-11
EP10162370.0 2010-05-10
EP10162370 2010-05-10

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EP (1) EP2509950B1 (fr)
JP (1) JP5797662B2 (fr)
KR (1) KR101771698B1 (fr)
CN (1) CN102770413B (fr)
AP (1) AP3217A (fr)
AR (1) AR079354A1 (fr)
AU (1) AU2010329867B2 (fr)
BR (1) BR112012013493B1 (fr)
CA (1) CA2783929C (fr)
DK (1) DK2509950T3 (fr)
EA (1) EA020758B1 (fr)
ES (1) ES2536774T3 (fr)
HK (1) HK1177454A1 (fr)
IL (1) IL219272A (fr)
JO (1) JO3090B1 (fr)
MX (1) MX2012006613A (fr)
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PL (1) PL2509950T3 (fr)
PT (1) PT2509950E (fr)
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TW (1) TWI485149B (fr)
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HK1177454A1 (en) 2013-08-23
BR112012013493A8 (pt) 2017-12-26
NZ599916A (en) 2013-10-25
BR112012013493A2 (pt) 2016-05-31
TWI485149B (zh) 2015-05-21
AP3217A (en) 2015-04-30
CA2783929C (fr) 2020-04-07
EA201290487A1 (ru) 2012-11-30
AU2010329867A1 (en) 2012-05-24
EA020758B1 (ru) 2015-01-30
AP2012006228A0 (en) 2012-04-30
IL219272A (en) 2014-09-30
PT2509950E (pt) 2015-06-08
JP2013513576A (ja) 2013-04-22
MX2012006613A (es) 2012-07-10
SG181609A1 (en) 2012-07-30
EP2509950A1 (fr) 2012-10-17
CN102770413A (zh) 2012-11-07
AU2010329867B2 (en) 2016-01-28
IL219272A0 (en) 2012-06-28
JP5797662B2 (ja) 2015-10-21
BR112012013493B1 (pt) 2020-12-08
TW201130823A (en) 2011-09-16
EP2509950B1 (fr) 2015-02-25
JO3090B1 (ar) 2017-03-15
AR079354A1 (es) 2012-01-18
CA2783929A1 (fr) 2011-06-16
KR101771698B1 (ko) 2017-08-25
PL2509950T3 (pl) 2015-10-30
ES2536774T3 (es) 2015-05-28
US8592429B2 (en) 2013-11-26
US20120295920A1 (en) 2012-11-22
CN102770413B (zh) 2015-08-26
DK2509950T3 (en) 2015-05-18
KR20120107104A (ko) 2012-09-28

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