WO2014033170A1 - Sulfamoyl-arylamides and the use thereof as medicaments for the treatment of hepatitis b - Google Patents

Sulfamoyl-arylamides and the use thereof as medicaments for the treatment of hepatitis b Download PDF

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Publication number
WO2014033170A1
WO2014033170A1 PCT/EP2013/067821 EP2013067821W WO2014033170A1 WO 2014033170 A1 WO2014033170 A1 WO 2014033170A1 EP 2013067821 W EP2013067821 W EP 2013067821W WO 2014033170 A1 WO2014033170 A1 WO 2014033170A1
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Prior art keywords
compound
mmol
alkyl
independently selected
group
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PCT/EP2013/067821
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French (fr)
Inventor
Stefaan Julien Last
Pierre Jean-Marie Bernard Raboisson
Geert Rombouts
Koen Vandyck
Wim Gaston Verschueren
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Janssen R&D Ireland
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Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=49085019&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=WO2014033170(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Priority to EA201590457A priority Critical patent/EA038942B1/en
Priority to KR1020217019832A priority patent/KR20210081451A/en
Priority to AP2015008249A priority patent/AP2015008249A0/en
Priority to SG11201501359TA priority patent/SG11201501359TA/en
Priority to AU2013307331A priority patent/AU2013307331A1/en
Priority to BR112015004192-2A priority patent/BR112015004192B1/en
Priority to EP13756110.6A priority patent/EP2890688A1/en
Priority to NZ704748A priority patent/NZ704748A/en
Priority to CN201380044856.2A priority patent/CN104812743A/en
Priority to KR1020207016380A priority patent/KR102271574B1/en
Priority to KR1020157005867A priority patent/KR102122357B1/en
Priority to US14/423,963 priority patent/US10676429B2/en
Priority to CA2880699A priority patent/CA2880699A1/en
Priority to MX2015002696A priority patent/MX2015002696A/en
Application filed by Janssen R&D Ireland filed Critical Janssen R&D Ireland
Priority to JP2015529005A priority patent/JP6505013B2/en
Priority to UAA201502767A priority patent/UA123256C2/en
Publication of WO2014033170A1 publication Critical patent/WO2014033170A1/en
Priority to IL236967A priority patent/IL236967A0/en
Priority to CR20150060A priority patent/CR20150060A/en
Priority to PH12015500317A priority patent/PH12015500317A1/en
Priority to HK15109247.5A priority patent/HK1208465A1/en
Priority to IL253225A priority patent/IL253225B/en
Priority to AU2018204597A priority patent/AU2018204597B2/en
Priority to PH12019502355A priority patent/PH12019502355A1/en
Priority to AU2020201203A priority patent/AU2020201203A1/en
Priority to US16/858,519 priority patent/US20200255373A1/en

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    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
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    • C07C311/15—Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings
    • C—CHEMISTRY; METALLURGY
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    • 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
    • C07C311/30—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound nitrogen atoms, not being part of nitro or nitroso groups
    • C07C311/37—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound nitrogen atoms, not being part of nitro or nitroso groups having the sulfur atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring
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    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/445—Non condensed piperidines, e.g. piperocaine
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Definitions

  • the Hepatitis B virus is an enveloped, partially double- stranded DNA (dsDNA) virus of the Hepadnavirus family (Hepadnaviridae). Its genome contains 4 overlapping reading frames: the precore/core gene; the polymerase gene; the L, M, and S genes, which encode for the 3 envelope proteins; and the X gene.
  • the partially double-stranded DNA genome (the relaxed circular DNA; rcDNA) is converted to a covalently closed circular DNA (cccDNA) in the nucleus of the host cell and the viral mRNAs are transcribed.
  • the pregenomic RNA (pgRNA), which also codes for core protein and Pol, serves as the template for reverse transcription, which regenerates the partially dsDNA genome (rcDNA) in the nucleocapsid.
  • HBV has caused epidemics in parts of Asia and Africa, and it is endemic in China. HBV has infected approximately 2 billion people worldwide of which approximately 350 million people have developed chronic infections. The virus causes the disease hepatitis B and chronic infection is correlated with a strongly increased risk for the development cirrhosis and hepatocellular carcinoma.
  • Transmission of hepatitis B virus results from exposure to infectious blood or body fluids, while viral DNA has been detected in the saliva, tears, and urine of chronic carriers with high titer DNA in serum.
  • heteroaryldihydropyrimidines were identified as a class of HBV inhibitors in tissue culture and animal models (Weber et al., Antiviral Res. 54: 69-78).
  • WO2013/006394 published on January 10, 2013, and WO2013/096744, published on June 27, 2013 relate to subclasses of Sulphamoyl-arylamides active against HBV.
  • HBV direct antivirals may encounter are toxicity, mutagenicity, lack of selectivity, poor efficacy, poor bioavailability and difficulty of synthesis.
  • HBV inhibitors may overcome at least one of these disadvantages or that have additional advantages such as increased potency or an increased safety window.
  • the present invention relates to compounds of Formula (I)
  • B represents a monocyclic 5 to 6 membered aromatic ring, optionally containing one or more heteroatoms each independently selected from the group consisting of O, S and N, such 5 to 6 membered aromatic ring optionally being substituted with one or more substituents each independently selected from the group consisting of hydrogen, halogen, Ci-C 3 alkyl, CN, CFH 2 , CF 2 H and CF 3 ;
  • Ri represents hydrogen or Ci-C 3 alkyl
  • Each R4 is independently selected from hydrogen, halogen, Ci-C 4 alkyloxy, Ci-C 4 alkyl, Ci-C 4 alkenyl, OH, CN, CFH 2 , CF 2 H, CF 3 , HC ⁇ C or a 3-5 membered saturated ring optionally containing one or more heteroatoms each independently selected from the group consisting of O and N, such Ci-C 4 alkyl optionally substituted with OH;
  • R 5 represents Ci-C 6 alkyl, CFH 2 , CF 2 H, CF 3i phenyl, pyridyl or a 3-7 membered
  • saturated ring optionally containing one or more heteroatoms each independently selected from the group consisting of O, S and N, such 3-7 membered saturated ring optionally being substituted with one or more substituents each independently selected from the group consisting of hydrogen, halogen, Ci-C 4 alkyloxy,
  • Ci-C 4 alkyloxycarbonyl, oxo, C( 0)-Ci-C 3 alkyl, Ci-C 4 alkyl, OH, CN, CFH 2 , CF 2 H and CF 3 ;
  • the invention further relates to a pharmaceutical composition
  • a pharmaceutical composition comprising a compound of Formula (I), and a pharmaceutically acceptable carrier.
  • the invention also relates to the compounds of Formula (I) for use as a medicament, preferably for use in the prevention or treatment of an HBV infection in a mammal.
  • the invention relates to a combination of a compound of Formula (I), and another HBV inhibitor.
  • Ci_ 3 alkyl or "Ci-C 3 alkyl” as a group or part of a group refers to a hydrocarbyl radical of Formula C n H 2n+ i wherein n is a number ranging from 1 to 3. In case Ci_ 3 alkyl is coupled to a further radical, it refers to a Formula C n H 2n ..
  • Ci_ 3 alkyl groups comprise from 1 to 3 carbon atoms, more preferably 1 to 2 carbon atoms.
  • Ci_ 3 alkyl includes all linear, or branched alkyl groups with between 1 and 3 carbon atoms, and thus includes such as for example methyl, ethyl, n-propyl, and /-propyl.
  • 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 the group defined for Ci_ 3 alkyl and butyl and the like.
  • Ci_ 6 alkyl as a group or part of a group defines straight or branched chain saturated hydrocarbon radicals having from 1 to 6 carbon atoms such as the groups defined for Ci_ 4 alkyl and pentyl, hexyl, 2-methylbutyl and the like.
  • Ci_ 4 alkenyl as a group or part of a group defines straight or branched chain
  • hydrocarbon radicals having from 1 to 4 carbon atoms with at least one double bond at any possible position.
  • alkenyls are ethenyl, propenyl, 1-butenyl, 2-butenyl.
  • Ci_ 6 alkenyl as a group or part of a group defines straight or branched chain hydrocarbon radicals having from 1 to 6 carbon atoms with at least one double bond.
  • Ci_3alkyloxy refers to a radical having the Formula— OR c wherein R c is Ci_ 3 alkyl.
  • suitable Ci_ 3 alkyloxy include methyloxy (also methoxy), ethyloxy (also ethoxy), propyloxy and
  • 3-7 membered saturated ring means saturated cyclic hydrocarbon with 3, 4, 5, 6 or 7 carbon atoms and is generic to cyclopropyl, eye lo butyl, cyclopentyl, cyclohexyl and cycloheptyl.
  • Such saturated ring optionally contains one or more heteroatoms, such that at least one carbon atom is replaced by a heteroatom selected from N, O and S, in particular from N and O.
  • heteroatoms such that at least one carbon atom is replaced by a heteroatom selected from N, O and S, in particular from N and O.
  • Examples include oxetane, azetidine, tetrahydro-2H-pyranyl, piperidinyl, tetrahydrofuranyl, morpholinyl and pyrrolidinyl.
  • Preferred are saturated cyclic hydrocarbon with 3 or 4 carbon atoms and 1 oxygen atom. Examples include oxetane and tetrahydrofuranyl.
  • the term monocyclic 5 to 6 membered aromatic ring (“aryl”) means an aromatic cyclic hydrocarbon with 5 or 6 carbon atoms.
  • a preferred example of an aryl group is phenyl.
  • Such saturated ring optionally contains one or more heteroatoms each independently selected from the group consisting of O, S and N("heteroaryl")
  • a heteroaryl group need only have some degree of aromatic character.
  • heteroaryl groups include, but are not limited to, pyridinyl, pyridazinyl, pyrimidyl, pyrazyl, triazinyl, pyrrolyl, pyrazolyl, imidazolyl, (1 ,2,3,)- and (l ,2,4)-triazolyl, pyrazinyl, pyrimidinyl, tetrazolyl, furyl, thienyl, isoxazolyl, thiazolyl, isoxazolyl, and oxazolyl.
  • a heteroaryl group can be unsubstituted or substituted with one or more suitable substituents.
  • 6-10 membered bicyclic ring indicates a saturated bi-cyclic ring with 6-7-8-9 or 10 atoms.
  • Such saturated bi-cyclic ring optionally contains one or more heteroatoms, such that at least one carbon atom is replaced by a heteroatom selected from N, O and S, in particular from N and O.
  • 6-10 membered bicyclic ring examples includeanl,4-dioxa-8- azaspiro[4.5] decyl moiety indicating a group with structural formula a 6-Oxa-2-azaspiro[3.4]octane moiety indicating a group with structural formula
  • 6-10 membered bridged ring indicates a saturated bridged ring with 6-7-8-9 or 10 atoms.
  • saturated bi-cyclic ring optionally contains one or more heteroatoms, such that at least one carbon atom is replaced by a heteroatom selected from N, O and S, in particular from N and O.
  • An example of such 6-10 membered bridged ring as used herein is -oxabicyclo[2.2.1]heptan represented by structure
  • a dihydroindenyl moiety represents a group with structural formula . Such dihydroindenyl moiety can be optionally substituted with OH.
  • a 2-hydroxy-2,3-dihydro-lH-indenyl moiety indicates a group with structural formula
  • a tetrahydronaphtalenyl moiety represents a group with structural formula
  • the attachment to the main structure may be anywhere on such moiety as long as it is chemically stable.
  • pyrrolyl may be lH-pyrrolyl or 2H-pyrrolyl.
  • halo and halogen are generic to fluoro, chloro, bromo or iodo. Preferred halogens are fluoro and Chloro. It should also be noted that the radical positions on any molecular moiety used in the definitions may be anywhere on such moiety as long as it is chemically stable. For instance pyridyl includes 2-pyridyl, 3-pyridyl and 4-pyridyl; pentyl includes 1-pentyl, 2-pentyl and 3-pentyl. Positions indicated on phenyl (e.g. ortho, meta and/or para) are indicated relative to the bond connecting the phenyl to the main structure. An example with regard to the position of R4, any location is indicated relative to the nitrogen (*) connected to the main structure:
  • the salts of the compounds of formula (I) are those wherein the counter ion is pharmaceutically or physiologically acceptable.
  • salts having a pharmaceutically unacceptable counter ion may also find use, for example, in the preparation or purification of a pharmaceutically acceptable compound of formula (I). All salts, whether pharmaceutically acceptable or not are included within the ambit of the present invention.
  • the pharmaceutically acceptable or physiologically tolerable addition salt forms which the compounds of the present invention are able to form can conveniently be prepared using the appropriate acids, such as, for example, inorganic acids such as hydrohalic acids, e.g. hydrochloric or hydrobromic acid; sulfuric; hemisulphuric, nitric; phosphoric and the like acids; or organic acids such as, for example, acetic, aspartic,
  • dodecylsulphuric heptanoic, hexanoic, nicotinic, propanoic, hydroxyacetic, lactic, pyruvic, oxalic, malonic, succinic, maleic, fumaric, malic, tartaric, citric,
  • salts also comprises the hydrates and the solvent addition forms that the compounds of the present invention are able to form. Examples of such forms are e.g. hydrates, alcoholates and the like.
  • stereochemically isomeric forms of compounds of the present invention defines all possible compounds made up of the same atoms bonded by the same sequence of bonds but having different three-dimensional structures which are not interchangeable, which the compounds of the present invention may possess.
  • chemical designation of a compound encompasses the mixture of all possible stereochemically isomeric forms which said compound may possess. Said mixture may contain all diastereomers and/or enantiomers of the basic molecular structure of said compound.
  • All stereochemically isomeric forms of the compounds of the present invention both in pure form or in admixture with each other are intended to be embraced within the scope of the present invention.
  • stereoisomeric forms of the compounds and intermediates as mentioned herein are defined as isomers substantially free of other enantiomeric or diastereomeric forms of the same basic molecular structure of said compounds or intermediates.
  • the term 'stereoisomerically pure' concerns compounds or intermediates having a stereoisomeric excess of at least 80% (i. e. minimum 90% of one isomer and maximum 10%) of the other possible isomers) up to a stereoisomeric excess of 100% (i.e. 100% of one isomer and none of the other), more in particular, compounds or intermediates having a stereoisomeric excess of 90% up to 100%, even more in particular having a stereoisomeric excess of 94% up to 100% and most in particular having a
  • enantiomers may be separated from each other by the selective crystallization of their diastereomeric salts with optically active acids or bases. Examples thereof are tartaric acid, dibenzoyltartaric acid, ditoluoyltartaric acid and camphosulfonic acid. Alternatively, enantiomers may be separated by chromatographic techniques using chiral stationary phases.
  • Said pure stereochemically isomeric forms may also be derived from the corresponding pure stereochemically isomeric forms of the appropriate starting materials, provided that the reaction occurs stereospecifically.
  • said compound will be synthesized by stereospecific methods of preparation. These methods will advantageously employ enantiomerically pure starting materials.
  • the diastereomeric racemates of formula (I) can be obtained separately by conventional methods. Appropriate physical separation methods that may advantageously be employed are, for example, selective crystallization and chromatography, e.g. column chromatography.
  • the present invention is also intended to include all isotopes of atoms occurring on the present compounds. Isotopes include those atoms having the same atomic number but different mass numbers.
  • isotopes of hydrogen include tritium and deuterium.
  • Isotopes of carbon include C-13 and C-14.
  • the present compounds or similar term is meant to include the compounds of general formula (I), (I*), (la) ,(Ib),(Ic) and (Id), salts, stereoisomeric forms and racemic mixtures or any subgroups thereof.
  • B represents a monocyclic 5 to 6 membered aromatic ring, optionally containing one or more heteroatoms each independently selected from the group consisting of O, S and N, such 5 to 6 membered aromatic ring optionally being substituted with one or more substituents each independently selected from the group consisting of hydrogen, halogen, Ci-C 3 alkyl, CN, CFH 2 , CF 2 H and CF 3 ;
  • Ri represents hydrogen or Ci-C 3 alkyl
  • Ci-C 4 alkyl OH, CN, CFH 2 , CF 2 H and CF 3 ;
  • Each R4 is independently selected from hydrogen, halogen, Ci-C 4 alkyloxy, Ci-C 4 alkyl, Ci-C 4 alkenyl, OH, CN, CFH 2 , CF 2 H, CF 3 , HC ⁇ C or a 3-5 membered saturated ring optionally containing one or more heteroatoms each independently selected from the group consisting of O and N, such Ci-C 4 alkyl optionally substituted with OH;
  • R 5 represents Ci-C 6 alkyl, CFH 2 , CF 2 H, CF 3i phenyl, pyridyl or a 3-7 membered
  • saturated ring optionally containing one or more heteroatoms each independently selected from the group consisting of O, S and N, such 3-7 membered saturated ring optionally being substituted with one or more substituents each independently selected from the group consisting of hydrogen, halogen, Ci-C 4 alkyloxy,
  • Ci-C 4 alkyloxycarbonyl, oxo, C( 0)-Ci-C 3 alkyl, Ci-C 4 alkyl, OH, CN, CFH 2 , CF 2 H and CF 3 ;
  • the invention further provides compound of Formula (I)
  • B represents a monocyclic 5 to 6 membered aromatic ring, optionally containing one or more heteroatoms each independently selected from the group consisting of O, S and N, such 5 to 6 membered aromatic ring optionally being substituted with one or more substituents each independently selected from the group consisting of hydrogen, halo, Ci-C 3 alkyl, CN, CFH 2 , CF 2 H and CF 3 ;
  • Ri represents hydrogen or Ci-C 3 alkyl
  • Ci-C 4 alkyl OH, CN, CFH 2 , CF 2 H and CF 3 ;
  • Each R4 is independently selected from hydrogen, halogen, Ci-C 4 alkyloxy, Ci-C 4 alkyl, Ci-C 4 alkenyl, OH, CN, CFH 2 , CF 2 H, CF 3 , HC ⁇ C or a 3-5 membered saturated ring optionally containing one or more heteroatoms each independently selected from the group consisting of O and N, such Ci-C 4 alkyl optionally substituted with OH;
  • R 5 represents Ci-Cealkyl, CFH 2 , CF 2 H, CF 3i phenyl, pyridyl or a 3-7 membered saturated ring optionally containing one or more heteroatoms each independently selected from the group consisting of O, S and N, such 3-7 membered saturated ring optionally being substituted with one or more substituents each independently selected from the group consisting of hydrogen, halogen, Ci-C 4 alkyloxy,
  • Ci-C 4 alkyloxycarbonyl, oxo, C( 0)-Ci-C 3 alkyl, Ci-C 4 alkyl, OH, CN, CFH 2 , CF 2 H and CF 3 ; or a pharmaceutically acceptable salt or a solvate thereof.
  • At least one R 4 represents Fluor, and one other R 4 is selected from the group consisting of Ci-C 3 alkyl, Ci-C 3 alkenyl, CHF 2 or cyclopropyl.
  • one R 4 represents Fluor and one other R 4 is selected from the group consisting of methyl or CHF 2i preferably methyl, and wherein the location of said Fluor is on the para position and the location of said methyl or CHF 2 is on the meta position related to the Nitrogen(*) as indicated In Formula (I*) below.
  • the invention provides compound of Formula (I) wherein at least one R 4 represents Fluor, and one other R 4 is selected from the group consisting of Ci-C 3 alkyl, Ci-C 3 alkenyl, CHF 2 or cyclopropyl; more preferably, one R 4 represents Fluor and one other R 4 is selected from the group consisting of methyl or CHF 2 and wherein the location of said Fluor is on the para position and the location of said methyl or CHF 2 is on the meta position related to the Nitrogen (*) and R 2 represents a 4-7 membered saturated ring containing carbon and one or more oxygen atoms, such 4-7 membered saturated ring optionally being substituted with one or more substituents each independently selected from the group consisting of hydrogen, halo, Ci-C 4 alkyl- oxy, Ci-C 4 alkyloxycarbonyl, Ci-C 4 alkyl, OH, CN, CFH 2 , CF 2 H and CF 3 .
  • R 2 represents a 4-7 membered saturated ring containing carbon and one or more oxygen atoms, such 4-7 membered saturated ring optionally being substituted with one or more substituents each independently selected from the group consisting of hydrogen, halogen, Ci-C 4 alkyloxy, Ci-C 4 alkyloxycarbonyl,
  • a preferred substituent for such a 4-7 membered saturated ring containing carbon and one or more oxygen atoms is Ci-C 4 alkyl.
  • the saturated ring is a 4, 5 or 6 membered ring.
  • R 2 represents a 4-7 membered saturated ring containing carbon and one or more nitrogen atoms, such 4-7 membered saturated ring optionally being substituted with one or more substituents each independently selected from the group consisting of hydrogen, halogen, Ci-C 4 alkyloxy, Ci-C 4 alkyloxycarbonyl ,
  • R 2 represents a 4-7 membered saturated ring containing carbon and one or more oxygen atoms, such 4-7 membered saturated ring optionally being substituted with one or more substituents each independently selected from the group consisting of hydrogen, halogen, Ci-C 4 alkyloxy, Ci-C 4 alkyloxycarbonyl, Ci-C 4 alkyl, OH, CN, CFH 2 , CF 2 H and CF 3 wherein such compound is not
  • Ci-C 6 alkyl-R 5 or Ci-C 6 alkyl is independently selected from the group consisting of hydrogen, Fluoro, OH, Ci-C 3 alkyl and CF 3 , most preferably from the group consisting of hydrigen Ci-C 3 alkyl, Fluoro and CF 3 .
  • compounds according to Formula (I) are provided wherein B represents phenyl or thiophene, optionally being substituted with one or more substituents each independently selected from the group consisting of hydrogen, halogen, Ci-C 3 alkyl, CN, CFH 2 , CF 2 H and CF 3 .
  • R ls R 2 , R4 are defined as in any one of the embodiments as described and R 3 is selected from the group comprising hydrogen, halogen, Ci-C 3 alkyl, CN, CFH 2 , CF 2 H, CF 3 .
  • R3 represents Fluor or hydrogen, more preferably hydrogen.
  • R l s R 2 and R4 are defined as in any one of the embodiments as described.
  • R l s R 2 and R4 are defined as in any one of the embodiments described and R3 is selected from the group comprising hydrogen, halogen, Ci-C 3 alkyl, CN, CFH 2 , CF 2 H, CF 3 .
  • the compounds according to the invention are envisioned for use in the prevention or treatment of an HBV infection in a mammal.
  • the present invention provides compounds which can be represented by Formula (I):
  • B represents a monocyclic 5 to 6 membered aromatic ring, optionally containing one or more heteroatoms each independently selected from the group consisting of O, S and N, such 5 to 6 membered aromatic ring optionally being substituted with one or more substituents each independently selected from the group consisting of hydrogen, halo, Ci-C 3 alkyl, CN, CFH 2 , CF 2 H and CF 3 ;
  • Ri represents hydrogen or Ci-C 3 alkyl
  • Each R4 is independently selected from hydrogen, halo, Ci-C 4 alkyloxy, Ci-C 4 alkyl, OH, CN, CFH 2 , CF 2 H, CF 3 , HC ⁇ C or a 3-5 membered saturated ring optionally containing one or more heteroatoms each independently selected
  • the invention relates to compounds according to Formula (I)
  • B represents a monocyclic 5 to 6 membered aromatic ring, optionally containing one or more heteroatoms each independently selected from the group consisting of O, S and N, such 5 to 6 membered aromatic ring optionally being substituted with one or more substituents each independently selected from the group consisting of hydrogen, halo, Ci-C 3 alkyl, CN, CFH 2 , CF 2 H and CF 3 ;
  • Ri represents hydrogen or Ci-C 3 alkyl
  • Each R4 is independently selected from hydrogen, halo, Ci-C 4 alkyloxy, Ci-C 4 alkyl, OH, CN, CFH 2 , CF 2 H, CF 3 , HC ⁇ C or a 3-5 membered saturated ring optionally containing one or more heteroatoms each independently selected from the group consisting of O and N;
  • the present invention additionally relates to compound of Formula (I) or a stereoisomer or tautomeric form thereof, or a pharmaceutically acceptable salt or a solvate thereof
  • B represents a monocyclic 5 to 6 membered aromatic ring, optionally containing one or more heteroatoms each independently selected from the group consisting of O, S and N, such 5 to 6 membered aromatic ring optionally being substituted with one or more substituents each independently selected from the group consisting of hydrogen, halo, Ci-C 3 alkyl, CN, CFH 2 , CF 2 H and CF 3 ;
  • Ri represents hydrogen or Ci-C 3 alkyl
  • Each R4 is independently selected from hydrogen, halo, Ci-C 4 alkyloxy, Ci-C 4 alkyl, OH, CN, CFH 2 , CF 2 H, CF 3 , HC ⁇ C or a 3-5 membered saturated ring optionally containing one or more heteroatoms each independently selected from the group consisting of O and N;
  • R 5 represents Ci-Cealkyl, CFH 2 , CF 2 H, CF 3 or a 3-7 membered saturated ring optionally containing one or more heteroatoms each independently selected from the group consisting of O, S and N, such 3-7 membered saturated ring optionally being substituted with one or more substituents each independently selected from the group consisting of hydrogen, halo, Ci-C 4 alkyloxy, oxo,
  • Ci-C 4 alkyl OH, CN, CFH 2 , CF 2 H and CF 3 ;
  • R l s R 2 , B are defined as above and each R4 is independently selected from hydrogen, halo, Ci-C 4 alkyloxy, Ci-C 4 alkyl, OH, CN, CFH 2 , CF 2 H, CF 3 or a 3-5 membered saturated ring optionally containing one or more heteroatoms each independently selected from the group consisting of O and N.
  • R 2 represents a 3-7 membered saturated ring, containing one or more heteroatoms each independently selected from the group consisting of O, S and N, such 3-7 membered saturated ring optionally being substituted with one or more substituents each independently selected from the group consisting of hydrogen, halo, Ci-C 4 alkyloxy, oxo, Ci-C 4 alkyl, OH, CN, CFH 2 , CF 2 H and CF 3 .
  • B represents phenyl or thiophene, optionally being substituted with one or more substituents each independently selected from the group consisting of hydrogen, halogen, Ci-C 3 alkyl, CN, CFH 2 , CF 2 H and CF 3 .
  • At least one R4 represents Fluor, Ci-C 3 alkyl, CHF 2 or cyclopropyl.
  • at least one R4 represents methyl, /-propyl or cyclopropyl.
  • one R4 represents methyl, /-propyl or cyclopropyl and the other R4 represents Fluor, or hydrogen.
  • the position of R4 preferably is meta and/or para (position indicated from -N ⁇ ).
  • One specific embodiment is a compound of Formula (I) wherein one R4 on the para position represents Fluor and the other one R4 on the meta position represents Fluor or methyl (position indicated from -N ⁇ ).
  • R l s R 2 , R4 are defined as above and R 3 is selected from the group comprising hydrogen, halo, Ci-C 3 alkyl, CN, CFH 2 , CF 2 H, CF 3 .
  • R 3 represents Fluor or hydrogen.
  • the invention further relates to compounds according to Formula (I)
  • B represents a monocyclic 5 to 6 membered aromatic ring, optionally containing one or more heteroatoms each independently selected from the group consisting of O, S and N, such 5 to 6 membered aromatic ring optionally being substituted with one or more substituents each independently selected from the group consisting of hydrogen, halo, Ci-C 3 alkyl, CN, CFH 2 , CF 2 H and CF 3 ;
  • Ri represents hydrogen or Ci-C 3 alkyl
  • R 2 represents Ci-C 3 alkyl-R 6 or a 4-7 membered saturated ring consisting of carbon atoms and one or more heteroatoms each independently selected from the group consisting of O or S, such 4-7 membered saturated ring optionally being substituted with one or more substituents each independently selected from the group consisting of hydrogen, halo, Ci-C 4 alkyloxy, oxo, Ci-C 4 alkyl, OH, CN, CFH 2 , CF 2 H and CF 3;
  • Each R4 is independently selected from hydrogen, halo, Ci-C 4 alkyloxy, Ci-C 4 alkyl, OH, CN, CFH 2 , CF 2 H, CF 3 , HC ⁇ C or a 3-5 membered saturated ring optionally containing one or more heteroatoms each independently selected from the group consisting of O and N;
  • R 6 represents a 4-7 membered saturated ring optionally containing one or more
  • heteroatoms each independently selected from the group consisting of O or S, such 4-7 membered saturated ring optionally being substituted with one or more substituents each independently selected from the group consisting of hydrogen, halo, Ci-C 4 alkyloxy, oxo, Ci-C 4 alkyl, OH, CN, CFH 2 , CF 2 H and CF 3 ;
  • R l s R 2 , B are defined as above and each R4 is independently selected from hydrogen, halo, Ci-C 4 alkyloxy, Ci-C 4 alkyl, OH, CN, CFH 2 , CF 2 H, CF 3 or a 3-5 membered saturated ring optionally containing one or more heteroatoms each independently selected from the group consisting of O and N.
  • R 2 represents Ci-C 3 alkyl-R6 or a 4-7 membered saturated ring consisting of carbon atoms and one or more heteroatoms each independently selected from the group consisting of O or S, such 4-7 membered saturated ring optionally being substituted with one or more substituents each independently selected from the group consisting of hydrogen, halo, Ci-C 4 alkyloxy, oxo, Ci-C 4 alkyl, OH, CN, CFH 2 , CF 2 H and CF 3 .
  • B represents phenyl or thiophene, optionally being substituted with one or more substituents each
  • At least one R 4 represents Fluor, Ci-C 3 alkyl ,CHF 2 or cyclopropyl.
  • at least one R 4 represents methyl, /-propyl or cyclopropyl.
  • one P represents methyl, /-propyl or cyclopropyl and the other R4 represents Fluor, or hydrogen.
  • the position of R4 preferably is meta and/or para.
  • One specific embodiment is a compound of Formula (I) wherein one R4 on the para position represents Fluor and the other one R4 on the meta position represents Fluor or methyl.
  • Ri represents hydrogen or Ci-C 3 alkyl
  • R 2 represents Ci-C 3 alkyl-R6 or a 4-7 membered saturated ring consisting of carbon atoms and one or more heteroatoms each independently selected from the group consisting of O or S, such 4-7 membered saturated ring optionally being substituted with one or more substituents each independently selected from the group consisting of hydrogen, halo, Ci-C 4 alkyloxy, oxo, Ci-C 4 alkyl, OH, CN, CFH 2 , CF 2 H and CF 3;
  • Each R4 is independently selected from hydrogen, halo, Ci-C 4 alkyloxy, Ci-C 4 alkyl, OH, CN, CFH 2 , CF 2 H, CF 3 or a 3-5 membered saturated ring optionally containing one or more heteroatoms each independently selected from the group consisting of O and N;
  • Re represents a 4-7 membered saturated ring optionally containing one or more
  • heteroatoms each independently selected from the group consisting of O or S, such
  • 4-7 membered saturated ring optionally being substituted with one or more substituents each independently selected from the group consisting of hydrogen, halo, Ci-C 4 alkyloxy, oxo, Ci-C 4 alkyl, OH, CN, CFH 2 , CF 2 H and CF 3 ;
  • R 3 is selected from the group comprising hydrogen, halo, Ci-C 3 alkyl, CN, CFH 2 , CF 2 H, CF 3 .
  • R 3 represents Fluor or hydrogen.
  • R ⁇ represents a 4-7 membered saturated ring consisting of carbon atoms and one or more heteroatoms each independently selected from the group consisting of O or S, such 4-7 membered saturated ring optionally being substituted with one or more substituents each independently selected from the group consisting of hydrogen, halo, Ci-C 4 alkyloxy, oxo, Ci-C 4 alkyl, OH, CN, CFH 2 , CF 2 H and CF 3 .
  • Preferred compounds according to the invention are compounds or a stereoisomer or tautomeric form thereof with a formula or reference to a formula selected from the following tables 1 and 2: Table 2.
  • the present invention concerns a pharmaceutical composition
  • a pharmaceutical composition comprising a therapeutically or prophylactically effective amount of a compound of Formula (I) as specified herein, and a pharmaceutically acceptable carrier.
  • a prophylactically effective amount in this context is an amount sufficient to prevent HBV infection in subjects being at risk of being infected.
  • a therapeutically effective amount in this context is an amount sufficient to stabilize HBV infection, to reduce HBV infection, or to eradicate HBV infection, in infected subjects.
  • this invention relates to a process of preparing a pharmaceutical composition as specified herein, which comprises intimately mixing a pharmaceutically acceptable carrier with a therapeutically or prophylactically effective amount of a compound of Formula (I), as specified herein.
  • 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 pharma- ceutically acceptable carrier, which carrier may take a wide variety of forms depending on the form of preparation desired for administration.
  • a pharma- ceutically acceptable carrier which carrier may take a wide variety of forms depending on the form of preparation desired for 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, 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 employed.
  • the carrier will usually comprise sterile water, at least in large part, though other ingredients, for example, to aid solubility, may be included.
  • injectable solutions for example, may be prepared in which the carrier comprises saline solution, glucose solution or a mixture of saline and glucose solution.
  • injectable suspensions may also be prepared in which case appropriate liquid carriers, suspending agents and the like may be employed.
  • solid form preparations intended to be converted, shortly before use, to liquid form preparations.
  • 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.
  • the compounds of the present invention may also be administered via oral inhalation or insufflation in the form of a solution, a suspension or a dry powder using any art-known delivery system. It is especially advantageous to formulate the aforementioned pharmaceutical compositions in unit dosage form for ease of administration and uniformity of dosage.
  • Unit dosage form as used herein 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, suppositories, powder packets, wafers, injectable solutions or suspensions and the like, and segregated multiples thereof.
  • the compounds of Formula (I) are active as inhibitors of the HBV replication cycle and can be used in the treatment and prophylaxis of HBV infection or diseases associated with HBV.
  • the latter include progressive liver fibrosis, inflammation and necrosis leading to cirrhosis, end-stage liver disease, and hepatocellular carcinoma.
  • the compounds of Formula (I) or any subgroup thereof are useful in the inhibition of the HBV replication cycle, in particular in the treatment of warm-blooded animals, in particular humans, infected with HBV, and for the prophylaxis of HBV infections.
  • the present invention furthermore relates to a method of treating a warm-blooded animal, in particular human, infected by HBV, or being at risk of infection by HBV, said method comprising the administration of a therapeutically effective amount of a compound of Formula (I).
  • the compounds of Formula (I), as specified herein, may therefore be used as a medicine, in particular as medicine to treat or prevent HBV infection.
  • Said use as a medicine or method of treatment comprises the systemic administration to HBV infected subjects or to subjects susceptible to HBV infection of an amount effective to combat the conditions associated with HBV infection or an amount effective to prevent HBV infection.
  • the present invention also relates to the use of the present compounds in the manufacture of a medicament for the treatment or the prevention of HBV infection.
  • an antiviral effective daily amount would be from about 0.01 to about 50 mg/kg, or about 0.01 to about 30 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 about 1 to about 500 mg, or about 1 to about 300 mg, or about 1 to about 100 mg, or about 2 to about 50 mg of active ingredient per unit dosage form.
  • the present invention also concerns combinations of a compound of Formula (I) or any subgroup thereof, as specified herein with other anti-HBV agents.
  • the term "combination” may relate to a product or kit containing (a) a compound of Formula (I), as specified above, and (b) at least one other compound capable of treating HBV infection (herein designated as anti-HBV agent), as a combined preparation for simultaneous, separate or sequential use in treatment of HBV infections.
  • anti-HBV agent a compound capable of treating HBV infection
  • the invention concerns combination of a compound of Formula (I) or any subgroup thereof with at least one anti-HBV agent.
  • the invention concerns combination of a compound of formula (I) or any subgroup thereof with at least two anti-HBV agents.
  • the invention concerns combination of a compound of formula (I) or any subgroup thereof with at least three anti-HBV agents. In a particular embodiment, the invention concerns combination of a compound of formula (I) or any subgroup thereof with at least four anti-HBV agents.
  • anti-HBV agents such as interferon-a (IFN-a), pegylated interferon-a, 3TC, adefovir or a combination thereof, and, a compound of formula (I) or any subgroup thereof can be used as a medicine in a combination therapy.
  • IFN-a interferon-a
  • 3TC pegylated interferon-a
  • adefovir a compound of formula (I) or any subgroup thereof
  • a compound of formula (I) or any subgroup thereof can be used as a medicine in a combination therapy.
  • a carboxylic acid chloride of general Formula II can be selectively reacted with an aniline of general formula III, for example in an organic solvent like CH 2 CI 2 in the presence of an organic base like triethylamine or DIPEA (N,N-diisopropylethylamine), or, as another example, by addition of the aniline III to a refluxing toluene solution of compound II, resulting in compound IV.
  • the remaining sulfonic acid chloride functionality in compound IV is further reacted with an amine of general formula V, resulting in a compound of general Formula (I).
  • a compound of general Formula (I) might be obtained as described in scheme 2.
  • the sulfonic acid chloride VI is reacted with an amine of general formula V, for example in an organic solvent like CH 2 CI 2 in the presence of an organic base like triethylamine or DIPEA or or, as another example, in the presence of Na 2 C0 3 in a mixture of H 2 O/THF.
  • the formed compound VII is coupled with aniline of general formula III in the presence of an activating reagent like for example HATU and an organic base like triethylamine or DIPEA.
  • compound IV can be reacted with an amino acid XI, in the presence of a base like NaOH, resulting in compound XII as described in scheme 4.
  • This intermediate XII can then optionally be cyclised to compound XIII for example by heating with acetic anhydride and KOAc in toluene, or converting the carboxylic acid to an acid chloride followed by cyclisation in the presence of a base like triethylamine.
  • Suitable examples of amino acids of structure XI are derivatives of 5-aminopentanoic acid or 4-aminobutanoic acid
  • a synthetic route to compounds of general formula XVI is described in Scheme 5.
  • a aminoethanol derivative XIV, prepared as described in scheme 1 for the compounds of general Formula (I), is transformed in a aziridine derivative XV by treatement with Diethyl diazene-l,2-dicarboxylate and PPh 3 in THF.
  • the aziridine of general formula XV is reacted with a nucleophile Nu, resulting in a compound of general formula XVI.
  • nucleophiles (Nu) are, but are not limited to, morpholine and 1-methylpiperazine.
  • Examples of a compound synthesized according to the route described in scheme 5, are compounds 116 and 117.
  • An alternative method for the synthesis of compounds of general formula VII is via ester XVII as described in scheme 6.
  • Reaction of XVII with amine V for example in an organic solvent like CH 2 CI 2 or THF in the presence of an organic base like for example triethylamine or DIPEA, followed by hydrolysis of the ester, for example with LiOH in THF/H 2 0, followed by acidification, results in a compound of general formula VII.
  • a compound of general formula VII, obtained via the route in scheme 2 or scheme 6, can be transformed to and acid chloride of formula XIX, for example by treatement with oxalyl chloride or thionyl chloride.
  • a compound of general formula XIX can then be transformed to a compound of general Formula (I) by reaction with an aniline of general formula III.
  • a compound of general formula VI can be converted to a compound of general formula II, for example by treatement with oxalyl chloride in CH 2 CI 2 .
  • compounds of general formula XXV or XXIV may be converted to compound of general formula XVII and VI respectively, by conversion to the corresponding diazonium salts (for example by NaN0 2 /HCl), followed by conversion of the diazonium salt to a sulfonyl chloride (for example by S0 2 /CuCl)(for example as described in Organic Process Research & Development, 13(5), 875-879; 2009).
  • compounds of general formula XXII and XXIII (with P 7 equaling H, benzyl or methyl) may be converted to compound of general formula XVII and VI respectively, for example by treatement with Cl 2 or N- Chlorosuccinimide in AcOH/H 2 0.
  • R4 in this general synthesis section are meant to include any substituent or reactive species that is suitable for transformation into any R4 subsitutent according to the present invention without undue burden for the person skilled in the art.
  • Method A mobile phase A : H 2 0 (0.1%TFA; B:CH 3 CN (0.05% TFA) Stop Time : 10 min; gradient time(min) [%A/%B] 0.0 [100/0] to 1 [100/0] to 5 [40/60] to 7.5
  • Method B mobile phase A : H 2 0 (0.1%TFA; B:CH 3 CN (0.05% TFA) Stop Time : 10 min; gradient time(min) [%A/%B] 0.0 [90/10] to 0.8 [90/10] to 4.5 [20/80] to 7.5 [20/80] to 8.0 [90/10]; flow: 0.8 mL/min; column temp.: 50°C, YMC-PACK ODS-AQ, 50x2.0mm 5 ⁇
  • Method C mobile phase A : H 2 0 (0.1 % TFA); B:CH 3 CN (0.05 % TFA) Stop Time : 10 min; gradient time(min) [%A/%B] 0.0 [90/10] to 0.8 [90/10] to 4.5 [20/80] to 7.5 [20/80]; 9.5 [90/10] flow: 0.8 mL/min; column temp.: 50°C; Agilent TC-C18, 50x2. lmm, 5 ⁇
  • Method D mobile phase A : H 2 0 (0.05 % NH 3 .H 2 0 ); B: CH 3 CN Stop Time : 10 min; gradient time(min) [%A/%B] 0.0 [100/0] to 1 [100/0] to 5 [40/60] to 7.5 [40/60]; 8 [100/0] flow: 0.8 mL/min; column temp.: 40 °C, XBridge Shield-RP18, 50*2. lmm 5 ⁇
  • Method E mobile phase A : H 2 0 (0.1%TFA; B:CH 3 CN (0.05% TFA) Stop Time : 10 min; Post Time: 0.5 min; gradient time(min) [%A/%B]0 [100/0] to 1 [100/0] to 5 [40/60] to 7.5 [15/85] to 9.5 [100/0]; flow: 0.8 mL/min; column temp.: 50°C, Agilent TC-C18, 50x2.1mm, 5 ⁇
  • Method F The LC measurement was performed using an Acquity UPLC (Waters) system with column heater (set at 55 °C). Reversed phase UPLC (Ultra Performance Liquid Chromatography) was carried out on a bridged ethylsiloxane/silica hybrid (BEH) C18 column (1.7 ⁇ , 2.1 x 50 mm; Waters Acquity) with a flow rate of 0.8 mL/min. Two mobile phases (10 mM ammonium acetate in H 2 0/acetonitrile 95/5; mobile phase B: acetonitrile) were used to run a gradient condition from 95 % A and 5 % B to 5 % A and 95 % B in 1.3 minutes and hold for 0.3 minutes. An injection volume of 0.5 ⁇ was used. Cone voltage was 10 V for positive ionization mode and 20 V for negative ionization mode.
  • Method G The LC measurement was performed using an Acquity UPLC (Waters) with column heater (set at 55 °C). Reversed phase UPLC (Ultra Performance Liquid
  • Method H Reversed phase HPLC was carried out on an Atlantis CI 8 column (3.5 ⁇ , 4.6 x 100 mm) with a flow rate of 1.6 mL/min. Column heater was set at 45 °C. Two mobile phases (mobile phase A: 70 % methanol + 30 % H 2 0; mobile phase B: 0.1 % formic acid in H 2 0/methanol 95/5) were employed to run a gradient condition from 100 % B to 5 % B + 95 % A in 9 minutes and hold these conditions for 3 minutes. An injection volume of 10 ⁇ was used. Cone voltage was 10 V for positive ionization mode and 20 V for negative ionization mode.
  • the residue was purified by column chromatography over silica gel (gradient eluent: petroleum ether/ethyl acetate from 100/0 to 10/90). The pure fractions were collected and the solvent was removed in vacuo. The residue was further purified by preparative high performance liquid chromatography over RP-18 (eluent: CH 3 CN in H 2 0 from 40% to 80%, v/v; 0.06% NH 4 HC0 3 as addition). The pure fractions were collected and the volatiles were removed in vacuo. The aqueous layer was lyophilized to dryness resulting in compound 9 (0.48 g) Method A; Rt: 4.6 min.
  • N-Ch I orosucc i n i mi do (2.56 g, 19.2 mmol ) was added to a mixture of 2-(benzylthio)-N-phenylisonicotinamide (1.5 g, 4.68 mmol) in acetic acid (20 mL) and water (10 mL). The reaction mixture was stirred at room temperature for 4 hours. The reaction was diluted with CH 2 CI 2 (20 mL). After washing with water, the organic layer was added to the mixture of cyclohexanamine (4.64 lg, 46.8 mmol) and Et 3 N (10 mL, 71.74 mmol) in CH 2 CI 2 (50mL). The resulting mixture was stirred at room temperature for 4 hours. The reaction mixture was washed with NH 4 CI
  • HATU (0.76 g, 2.0 mmol) was then added to a mixture of 4-(N-cyclohexylsulfamoyl)- picolinic acid (380 mg, 1.34 mmol), aniline (251 mg, 2.7 mmol) and DIPEA (0.517 g, 4.0 mmol) in DMF (50 mL) at room temperature The resulting mixture was stirred at room temperature for 18 hour. The mixture was diluted with water (200 mL), and extracted with EtOAc. The organic layers were washed with brine, dried over MgS0 4 , filtered and concentrated in vacuo.
  • the mixture B was added portionwise to the mixture A over 30 minutes, maintaining temperature at -5°C to 0°C.After stirring at 0°C for 1 hour, the solid was collected by filtration, washed with water, and dried in vacuo resulting in 5-(chlorosulfonyl)nicotinic acid (1.05 g).
  • reaction mixture was filtered through celite. Water (10 mL) was added to the filtrate and the mixture was extracted with ethyl acetate (2 x 10 mL). The combined organic layers were washed with brine and dried over Na 2 S0 4 . The solvent was removed in vacuo. The residue was purified by preparative high
  • N-(4-fluoro-3-((trimethylsilyl)ethynyl)phenyl)-3-(N-isopropylsulfamoyl)benzamide (0.8g, 1.66mmol) and TFA (4 mL) were dissolved in anhydrous CH 2 CI 2 (16 mL). The mixture was stirred at 25° overnight. The mixture was concentrated resulting in crude N-(3-ethynyl-4-fluorophenyl)-3-(N-isopropylsulfamoyl)benzamide which was used as such in the next step (650 mg).
  • the reaction mixture was diluted with ethyl acetate (20 mL) and the catalyst was filtered off. The filtrate was concentrated in vacuo. Water (20 mL) was added and the aqueous layer was extracted with ethyl acetate (2 x 20 mL). The combined organic layers were washed with brine and dried over Na 2 S0 4 . The solvent was removed in vacuo and the obtained residue was purified by preparative high performance liquid chromatography over reversed phase C-18 (eluent: CH 3 CN in H 2 0 (0.1 % TFA) from 40% to 70%, v/v). The pure fractions were collected and the organic solvent was removed in vacuo.
  • N-(4-fluoro-3-(prop-l-en-2-yl)phenyl)-3-(N-iso- propylsulfamoyl)benzamide 300 mg.
  • N-(4-fluoro-3-(prop-l-en-2-yl)phenyl)-3- (N-isopropylsulfamoyl)benzamide (180 mg) and Pd/C(wet) (20 mg) were stirred in methanol (4 mL) under a hydrogen atmosphere at 25°C for 3 hours. The mixture was filtered over celite and the filtrate was evaporated to dryness in vacuo.
  • 3-methyloxetan-3-amine hydrochloride (210 mg, 1.7 mmol) and NaOH (204 mg, 5.1 mmol) were dissolved in 2-methyltetrahydrofuran (5 mL) and H 2 0 (5 mL).
  • Compound 224 was prepared similarly as described for compound 223, using l-(4- pyridyl)propan-2-amine instead of l-(2-pyridyl)propan-2-amine.
  • Compound 224 was purified by preparative high-performance liquid chromatography (column: Luna 150*30mm*4u, mobile phase: CH 3 CN in water (0.05% NH 4 HC0 3 ) from 40% to 70%). Method A; Rt: 4.6 min. m/z: 428.3 (M+H) + Exact mass: 427.1.
  • Oxalyl chloride (18.3 mL, 213 mmol) was added in four portions over one hour.
  • Procedure SI A solution of 3-[(4-fluoro-3-methyl-phenyl)carbamoyl]benzenesulfonyl chloride (0.50 g, 1.52 mmol, 1 eq) in toluene (10 mL) was added to a flask containing an amine (1.1 eq). DIPEA (657 ⁇ , 3.81 mmol, 2.5 eq) was added and the reaction mixture was stirred for 1 hour. Next, 1M HC1 (5 mL) was added to the reaction mixture.
  • Procedure S2 A tube was charged with 3-[(4-fluoro-3-methyl-phenyl)carbamoyl]- benzenesulfonyl chloride (250 mg, 0.76 mmol) and an amine (1.1 eq) and CH 2 C1 2 (5 mL) was added. The solution was stirred, DIPEA (329 ⁇ , 1.9 mmol, 2.5 eq) was added and the mixture was further stirred for 30 minutes. Then, HC1 (1M aq / 5 mL) was added and the mixture was stirred for 5 minutes more.
  • Workup W3 The layers were separated and the organic layer was loaded on a silica gel column for purification (with gradient elution: CH 2 Cl 2 -methanol 100:0 to 97:3).
  • Workup W4 The organic layer was separated and loaded on a silica gel column. The mixture was purified using gradient elution from heptane to EtOAc.
  • Cis Enantiomers 134a and 134b N-(4-fluoro-3-methyl-phenyl)-3- [[(lR,3S)-3-hydroxycyclohexyl]sulfamoyl]benzamide or N-(4-fluoro-3-methyl- phenyl)-3-[[(lS,3R)-3-hydroxycyclohexyl]sulfamoyl]benzamide.
  • 141a, 141c N-(4-fiuoro-3-methyl-phenyl)-3-[[(lS,2S)-l-hydroxyindan-2-yl]- sulfamoyl]benzamide or N-(4-fluoro-3-methyl-phenyl)-3-[[(lR,2R)-l-hydroxyindan-2- yl]sulfamoyl]benzamide.
  • 141b, 141d N-(4-fluoro-3-methyl-phenyl)-3-[[(li?,25)-l-hydroxyindan-2- yl]sulfamoyl]benzamide or N-(4-fluoro-3 -methyl-phenyl)-3 - [ [( 1 S ,2R)- 1 -hydroxyindan- 2-yl]sulfamoyl]benzamide.
  • Racemic compound 179 was separated in enantiomers 179a and 179b by Preparative SFC (Stationary phase: Chiralpak Diacel AD 30 x 250 mm), Mobile phase: C0 2 , iPrOH with 0.4% iPrNH 2 ) The collected fractions were concentrated in vacuo resulting in compound 179a and 179b.
  • 179a +6.1 ° (589 nm, c 0.6225 w/v %, MeOH, 20 °C).
  • 179b -6.1 ° (589 nm, c 0.506 w/v %, MeOH, 20°C).
  • 3-(isopropylsulfamoyl)benzoic acid 250 mg, 1.03 mmol
  • 4-fluoro-3,5-dimethyl- aniline 157 mg, 1.13 mmol
  • DIPEA 398 mg, 3.08 mmol
  • acetonitrile 10 mL
  • HATU 430 mg, 1.13 mmol
  • EtOAc 100 mL was added and the mixture was washed with 1M HC1, sat NaHC0 3 and brine.
  • the reaction mixture was poured into H 2 0 (850 mL), and EtOAc (300 mL) was added. The mixture was stirred vigorously for 5 minutes. Both upper liquid layers were decanted from a residue. The separated water layer was combined with the residue, and extracted with EtOAc. Both upper liquid layers were decanted from the residue. The separated water layer was combined with the residue, and extracted again with EtOAc. The organic layers were combined, washed with satured NaCl and dried with Na 2 S0 4 , filtered off, evaporated, and co-evaporated with toluene.
  • the separated waterlayer was acidified with IN HC1 (30 mL), and the product was extracted with 2-MeTHF.
  • the separated waterlayer was acidified further till pH ⁇ 2 and extracted with 2-MeTHF.
  • the organic layer was washed with brine, dried with Na 2 S0 4 and filtered, resulting in crude 5-bromo-2-fluoro-6-methyl-3-[[(3S)-tetrahydrofuran-3- yl]sulfamoyl]benzoic acid (6.5 g).
  • Triethylamine (0.206 mL, 0.00149 mol ) was added to a stirring mixture of 2-fluoro-6- methyl-3-[(3-methyloxetan-3-yl)sulfamoyl]benzoic acid (0.15 g, 0.000495 mol ) and CH 3 CN (10 mL ) under N 2 -atm.
  • HATU 0.207 g, 0.545 mmol
  • 5-amino-2-fluorobenzonitrile (79.9 mg, 0.569 mmol ) was added, and the reaction mixture was stirred at room temperature for 20 hours. The reaction was next continued at 50°C for 4 hours.
  • Compound 192 was prepared similarly as described for compound 191, using 3-chloro- 4,5-dif uoro-aniline hydrochloride instead of 5-amino-2-fluorobenzonitrile.
  • 3-(tert-butylsulfamoyl)-2-fluoro-6-methyl-benzoic acid was prepared similarly as described for 2-fluoro-6-methyl-3-[(3-methyloxetan-3-yl)sulfamoyl]benzoic acid, using tert-butylamine instead of 3-methyloxetan-3-amine.
  • Compound 205 was prepared similar as described for compound 194, using 4-fluoro-3-methylaniline instead of 3,4- difluoroaniline and starting from 3-(tert-butylsulfamoyl)-2-fluoro-6-methyl-benzoic acid instead of 2-fluoro-6-methyl-3-[(3-methyloxetan-3-yl)sulfamoyl]benzoic acid.
  • 2-bromo-6-fluoro-3-[(3-methyloxetan-3-yl)sulfamoyl]benzoic acid and 6-bromo-2- fluoro-3-[(3-methyloxetan-3-yl)sulfamoyl]benzoic acid were prepared similarly as described for 2-chloro-6-fluoro-3-[(3-methyloxetan-3-yl)sulfamoyl]benzoic acid and 6- chloro-2-fluoro-3-[(3-methyloxetan-3-yl)sulfamoyl]benzoic acid, starting from 2- bromo-6-fluorobenzoic acid instead of 2-chloro-6-fluorobenzoic acid.
  • Compound 212 was prepared similarly as described for compound 196 using 2-bromo- 6-fluoro-3-[(3-methyloxetan-3-yl)sulfamoyl]benzoic acid instead of 2,6-difluoro-3- [[(35)-tetrahydrofuran-3-yl]sulfamoyl]benzoic acid and 4-fluoro-3- (trifluoromethyl)aniline instead of 3,4-difluoroaniline.
  • 3-methyl-3-oxetanamine (580 mg, 6.66 mmol) was added dropwise to the above solution at room temperature.
  • Et 3 N (2.10 mL 15.14 mmol) was then added dropwise to the reaction mixture and the reaction mixture was stirred at room temperature for 45 minutes. The solvent was evaporated and the residue was taken up in EtOAc.
  • HC1 (0.5 N, 30 mL) was added to the reaction mixture and the layers were separated. The organic layer was washed again with NaOH (0.5 N, 30 mL).
  • 3-methyloxolan-3-amine hydrochloride (165.9 mg, 1.21 mmol) was added to a solution of 3-[(4-fluoro-3-methyl-phenyl)carbamoyl]benzenesulfonyl chloride (499 mg, 1.096 mmol) in dry CH 2 CI 2 (20 mL) at room temperature.
  • Et 3 N (381 ⁇ ) was then added dropwise to the reaction mixture and the reaction mixture was stirred at room temperature for 1 hour. The reaction mixture was diluted with EtOAc (250 mL).
  • Compound 232 to 239 were prepared by slow addition of an aniline to a refluxing toluene solution of a 3-chlorosulfonylbenzoyl chloride derivative, followed by reaction with an amine in the presence of a base like NEt 3 or DIPEA, as described above.
  • the anti-HBV activity was measured using a stable transfected cell line
  • HepG2.2.15 This cell line was described to secrete relatively consistent high levels of HBV virion particles, which have been shown to cause both acute and chronic infection and disease in chimpanzees.
  • antiviral activity was determined by quantification of purified HBV DNA from secreted virions using realtime PCR and an HBV specific primer set and probe.
  • Cytotoxicity of the compounds was tested in HepG2 cells using CellTiter-Blue, with the same incubation period and dose range as in the HepG2.2.15 assay.
  • the anti HBV activity was also measured using the HepG2.117 cell line, a stable, inducibly HBV producing cell line, which replicates HBV in the absence of doxicycline (Tet-off system).
  • HBV replication was induced, followed by a treatment with serially diluted compound in 96-well plates in duplicate. After 3 days of treatment, the antiviral activity was determined by quantification of intracellular HBV DNA using realtime PCR and an HBV specific primer set and probe.

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Abstract

Inhibitors of HBV replication of Formula (I) including stereochemically isomeric forms, and salts, hydrates, solvates thereof, wherein B, R1, R2 and R4 have the meaning as defined herein. The present invention also relates to pharmaceutical compositions containing these inhibitors and to their use, alone or in combination with other HBV inhibitors, in HBV therapy.

Description

SULFAMOYL-ARYL AMIDES AND THE USE THEREOF AS MEDICAMENTS FOR THE TREATMENT OF HEPATITIS B.
Background Art
The Hepatitis B virus (HBV) is an enveloped, partially double- stranded DNA (dsDNA) virus of the Hepadnavirus family (Hepadnaviridae). Its genome contains 4 overlapping reading frames: the precore/core gene; the polymerase gene; the L, M, and S genes, which encode for the 3 envelope proteins; and the X gene.
Upon infection, the partially double-stranded DNA genome (the relaxed circular DNA; rcDNA) is converted to a covalently closed circular DNA (cccDNA) in the nucleus of the host cell and the viral mRNAs are transcribed. Once encapsidated, the pregenomic RNA (pgRNA), which also codes for core protein and Pol, serves as the template for reverse transcription, which regenerates the partially dsDNA genome (rcDNA) in the nucleocapsid.
HBV has caused epidemics in parts of Asia and Africa, and it is endemic in China. HBV has infected approximately 2 billion people worldwide of which approximately 350 million people have developed chronic infections. The virus causes the disease hepatitis B and chronic infection is correlated with a strongly increased risk for the development cirrhosis and hepatocellular carcinoma.
Transmission of hepatitis B virus results from exposure to infectious blood or body fluids, while viral DNA has been detected in the saliva, tears, and urine of chronic carriers with high titer DNA in serum.
An effective and well-tolerated vaccine exists, but direct treatment options are currently limited to interferon and the following antivirals; tenofovir, lamivudine, adefovir, entecavir and telbivudine.
In addition, heteroaryldihydropyrimidines (HAPs) were identified as a class of HBV inhibitors in tissue culture and animal models (Weber et al., Antiviral Res. 54: 69-78).
WO2013/006394, published on January 10, 2013, and WO2013/096744, published on June 27, 2013 relate to subclasses of Sulphamoyl-arylamides active against HBV.
Amongst the problems which HBV direct antivirals may encounter are toxicity, mutagenicity, lack of selectivity, poor efficacy, poor bioavailability and difficulty of synthesis. There is a need for additional HBV inhibitors that may overcome at least one of these disadvantages or that have additional advantages such as increased potency or an increased safety window. Description of the Invention
The present invention relates to compounds of Formula (I)
Figure imgf000003_0001
or a stereoisomer or tautomeric form thereof, wherein:
B represents a monocyclic 5 to 6 membered aromatic ring, optionally containing one or more heteroatoms each independently selected from the group consisting of O, S and N, such 5 to 6 membered aromatic ring optionally being substituted with one or more substituents each independently selected from the group consisting of hydrogen, halogen, Ci-C3alkyl, CN, CFH2, CF2H and CF3;
Ri represents hydrogen or Ci-C3alkyl;
R2 represents Ci-C6alkyl, Ci-C6alkenyl, Ci-C6alkyl-R5, C(=0)-R5, CFH2, CF2H, CF3, a dihydro-indenyl or tetrahydronaphtalenyl moiety optionally substituted with OH, or a 3-7 membered saturated ring optionally containing one or more heteroatoms each independently selected from the group consisting of O, S and N, such 3-7 membered saturated ring, Ci-C6alkyl-R5 or Ci-C6alkyl optionally being substituted with one or more substituents each independently selected from the group consisting of hydrogen, halogen, Ci-C4alkyloxy, Ci-C4alkyloxycarbonyl, oxo, C(=0)-Ci-C3alkyl, Ci-C4alkyl, OH, CN, CFH2, CF2H and CF3;
Or Ri and R2 together with the Nitrogen to which they are attached form a 6-10 membered bicyclic or bridged ring or a 5-7 membered saturated ring, such bicyclic, bridged or saturated ring moiety optionally containing one or more additional heteroatoms each independently selected from the group consisting of O, S and N, such 5-7 membered saturated ring optionally being substituted with one or more substituents each independently selected from the group consisting of hydrogen, halogen, Ci-C4alkyloxy, Ci-C4alkyloxycarbonyl, oxo, C(=0)-Ci-C3alkyl,
Ci-C4alkyl, OH, CN, CFH2, CF2H and CF3; Each R4 is independently selected from hydrogen, halogen, Ci-C4alkyloxy, Ci-C4alkyl, Ci-C4alkenyl, OH, CN, CFH2, CF2H, CF3 , HC≡C or a 3-5 membered saturated ring optionally containing one or more heteroatoms each independently selected from the group consisting of O and N, such Ci-C4alkyl optionally substituted with OH;
R5 represents Ci-C6alkyl, CFH2, CF2H, CF3i phenyl, pyridyl or a 3-7 membered
saturated ring optionally containing one or more heteroatoms each independently selected from the group consisting of O, S and N, such 3-7 membered saturated ring optionally being substituted with one or more substituents each independently selected from the group consisting of hydrogen, halogen, Ci-C4alkyloxy,
Ci-C4alkyloxycarbonyl, oxo, C(=0)-Ci-C3alkyl, Ci-C4alkyl, OH, CN, CFH2, CF2H and CF3;
or a pharmaceutically acceptable salt or a solvate thereof. The invention further relates to a pharmaceutical composition comprising a compound of Formula (I), and a pharmaceutically acceptable carrier.
The invention also relates to the compounds of Formula (I) for use as a medicament, preferably for use in the prevention or treatment of an HBV infection in a mammal.
In a further aspect, the invention relates to a combination of a compound of Formula (I), and another HBV inhibitor.
Definitions
The term "Ci_3alkyl" or "Ci-C3alkyl" as a group or part of a group refers to a hydrocarbyl radical of Formula CnH2n+i wherein n is a number ranging from 1 to 3. In case Ci_3alkyl is coupled to a further radical, it refers to a Formula CnH2n.. Ci_3alkyl groups comprise from 1 to 3 carbon atoms, more preferably 1 to 2 carbon atoms. Ci_ 3alkyl includes all linear, or branched alkyl groups with between 1 and 3 carbon atoms, and thus includes such as for example methyl, ethyl, n-propyl, and /-propyl.
Ci_4alkyl 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 the group defined for Ci_3 alkyl and butyl and the like.
Ci_6alkyl as a group or part of a group defines straight or branched chain saturated hydrocarbon radicals having from 1 to 6 carbon atoms such as the groups defined for Ci_4alkyl and pentyl, hexyl, 2-methylbutyl and the like. Ci_4alkenyl as a group or part of a group defines straight or branched chain
hydrocarbon radicals having from 1 to 4 carbon atoms with at least one double bond at any possible position. Examples of such alkenyls are ethenyl, propenyl, 1-butenyl, 2-butenyl. Ci_6alkenyl as a group or part of a group defines straight or branched chain hydrocarbon radicals having from 1 to 6 carbon atoms with at least one double bond.
The term "Ci_3alkyloxy" as a group or part of a group refers to a radical having the Formula— ORc wherein Rc is Ci_3alkyl. Non-limiting examples of suitable Ci_3alkyloxy include methyloxy (also methoxy), ethyloxy (also ethoxy), propyloxy and
isopropyloxy.
The term oxo, C(=0), or carbonyl refers to a group composed of a carbon atom double bonded to an oxygen atom. As used herein, the term "3-7 membered saturated ring" means saturated cyclic hydrocarbon with 3, 4, 5, 6 or 7 carbon atoms and is generic to cyclopropyl, eye lo butyl, cyclopentyl, cyclohexyl and cycloheptyl.
Such saturated ring optionally contains one or more heteroatoms, such that at least one carbon atom is replaced by a heteroatom selected from N, O and S, in particular from N and O. Examples include oxetane, azetidine, tetrahydro-2H-pyranyl, piperidinyl, tetrahydrofuranyl, morpholinyl and pyrrolidinyl. Preferred are saturated cyclic hydrocarbon with 3 or 4 carbon atoms and 1 oxygen atom. Examples include oxetane and tetrahydrofuranyl. As used herein, the term monocyclic 5 to 6 membered aromatic ring ("aryl"), means an aromatic cyclic hydrocarbon with 5 or 6 carbon atoms. A preferred example of an aryl group is phenyl.
Such saturated ring optionally contains one or more heteroatoms each independently selected from the group consisting of O, S and N("heteroaryl") For the purposes of the invention, a heteroaryl group need only have some degree of aromatic character.
Illustrative examples of heteroaryl groups include, but are not limited to, pyridinyl, pyridazinyl, pyrimidyl, pyrazyl, triazinyl, pyrrolyl, pyrazolyl, imidazolyl, (1 ,2,3,)- and (l ,2,4)-triazolyl, pyrazinyl, pyrimidinyl, tetrazolyl, furyl, thienyl, isoxazolyl, thiazolyl, isoxazolyl, and oxazolyl. A heteroaryl group can be unsubstituted or substituted with one or more suitable substituents.
As used herein, the term 6-10 membered bicyclic ring indicates a saturated bi-cyclic ring with 6-7-8-9 or 10 atoms. Such saturated bi-cyclic ring optionally contains one or more heteroatoms, such that at least one carbon atom is replaced by a heteroatom selected from N, O and S, in particular from N and O.
Examples of such 6-10 membered bicyclic ring as used herein areanl,4-dioxa-8- azaspiro[4.5] decyl moiety indicating a group with structural formula
Figure imgf000006_0001
a 6-Oxa-2-azaspiro[3.4]octane moiety indicating a group with structural formula
Figure imgf000006_0002
a 2-oxa-6-azaspiro[3.3]heptyl moiety indicating a group with structural formula
a 6-oxa-l-azaspiro[3.3]heptyl moiety with structural formula
Figure imgf000006_0003
As used herein, the term 6-10 membered bridged ring indicates a saturated bridged ring with 6-7-8-9 or 10 atoms. Such saturated bi-cyclic ring optionally contains one or more heteroatoms, such that at least one carbon atom is replaced by a heteroatom selected from N, O and S, in particular from N and O. An example of such 6-10 membered bridged ring as used herein is -oxabicyclo[2.2.1]heptan represented by structure
Figure imgf000006_0004
As used herein, a dihydroindenyl moiety represents a group with structural formula
Figure imgf000007_0001
. Such dihydroindenyl moiety can be optionally substituted with OH. One example as used herein, a 2-hydroxy-2,3-dihydro-lH-indenyl moiety, indicates a group with structural formula
Figure imgf000007_0002
As used herein, a tetrahydronaphtalenyl moiety represents a group with structural formula
Figure imgf000007_0003
If not indicated, for any of the moieties above, the attachment to the main structure may be anywhere on such moiety as long as it is chemically stable.
It should be noted that different isomers of the various heterocycles may exist within the definitions as used throughout the specification. For example, pyrrolyl may be lH-pyrrolyl or 2H-pyrrolyl.
The term halo and halogen are generic to fluoro, chloro, bromo or iodo. Preferred halogens are fluoro and Chloro. It should also be noted that the radical positions on any molecular moiety used in the definitions may be anywhere on such moiety as long as it is chemically stable. For instance pyridyl includes 2-pyridyl, 3-pyridyl and 4-pyridyl; pentyl includes 1-pentyl, 2-pentyl and 3-pentyl. Positions indicated on phenyl (e.g. ortho, meta and/or para) are indicated relative to the bond connecting the phenyl to the main structure. An example with regard to the position of R4, any location is indicated relative to the nitrogen (*) connected to the main structure:
Figure imgf000008_0001
(Formula (I*) When any variable (e.g. halogen or Ci_4alkyl) occurs more than one time in any constituent, each definition is independent.
For therapeutic use, the salts of the compounds of formula (I) are those wherein the counter ion is pharmaceutically or physiologically acceptable. However, salts having a pharmaceutically unacceptable counter ion may also find use, for example, in the preparation or purification of a pharmaceutically acceptable compound of formula (I). All salts, whether pharmaceutically acceptable or not are included within the ambit of the present invention. The pharmaceutically acceptable or physiologically tolerable addition salt forms which the compounds of the present invention are able to form can conveniently be prepared using the appropriate acids, such as, for example, inorganic acids such as hydrohalic acids, e.g. hydrochloric or hydrobromic acid; sulfuric; hemisulphuric, nitric; phosphoric and the like acids; or organic acids such as, for example, acetic, aspartic,
dodecylsulphuric, heptanoic, hexanoic, nicotinic, propanoic, hydroxyacetic, lactic, pyruvic, oxalic, malonic, succinic, maleic, fumaric, malic, tartaric, citric,
methanesulfonic, ethanesulfonic, benzenesulfonic, /?-toluenesulfonic, cyclamic, salicylic, /?-amino salicylic, pamoic and the like acids. Conversely said acid addition salt forms can be converted by treatment with an appropriate base into the free base form.
The term "salts" also comprises the hydrates and the solvent addition forms that the compounds of the present invention are able to form. Examples of such forms are e.g. hydrates, alcoholates and the like.
The present compounds may also exist in their tautomeric forms for example, tautomeric forms of amide (-C(=0)-NH-) groups are iminoalcohols (-C(OH)=N-). Tautomeric forms, although not explicitly indicated in the structural formulae represented herein, are intended to be included within the scope of the present invention.
The term stereochemically isomeric forms of compounds of the present invention, as used hereinbefore, defines all possible compounds made up of the same atoms bonded by the same sequence of bonds but having different three-dimensional structures which are not interchangeable, which the compounds of the present invention may possess. Unless otherwise mentioned or indicated, the chemical designation of a compound encompasses the mixture of all possible stereochemically isomeric forms which said compound may possess. Said mixture may contain all diastereomers and/or enantiomers of the basic molecular structure of said compound. All stereochemically isomeric forms of the compounds of the present invention both in pure form or in admixture with each other are intended to be embraced within the scope of the present invention.
Pure stereoisomeric forms of the compounds and intermediates as mentioned herein are defined as isomers substantially free of other enantiomeric or diastereomeric forms of the same basic molecular structure of said compounds or intermediates. In particular, the term 'stereoisomerically pure' concerns compounds or intermediates having a stereoisomeric excess of at least 80% (i. e. minimum 90% of one isomer and maximum 10%) of the other possible isomers) up to a stereoisomeric excess of 100% (i.e. 100% of one isomer and none of the other), more in particular, compounds or intermediates having a stereoisomeric excess of 90% up to 100%, even more in particular having a stereoisomeric excess of 94% up to 100% and most in particular having a
stereoisomeric excess of 97% up to 100%. The terms 'enantiomerically pure' and
'diastereomerically pure' should be understood in a similar way, but then having regard to the enantiomeric excess, respectively the diastereomeric excess of the mixture in question. Pure stereoisomeric forms of the compounds and intermediates of this invention may be obtained by the application of art-known procedures. For instance, enantiomers may be separated from each other by the selective crystallization of their diastereomeric salts with optically active acids or bases. Examples thereof are tartaric acid, dibenzoyltartaric acid, ditoluoyltartaric acid and camphosulfonic acid. Alternatively, enantiomers may be separated by chromatographic techniques using chiral stationary phases. Said pure stereochemically isomeric forms may also be derived from the corresponding pure stereochemically isomeric forms of the appropriate starting materials, provided that the reaction occurs stereospecifically. Preferably, if a specific stereoisomer is desired, said compound will be synthesized by stereospecific methods of preparation. These methods will advantageously employ enantiomerically pure starting materials. The diastereomeric racemates of formula (I) can be obtained separately by conventional methods. Appropriate physical separation methods that may advantageously be employed are, for example, selective crystallization and chromatography, e.g. column chromatography. The present invention is also intended to include all isotopes of atoms occurring on the present compounds. Isotopes include those atoms having the same atomic number but different mass numbers. By way of general example and without limitation, isotopes of hydrogen include tritium and deuterium. Isotopes of carbon include C-13 and C-14. Detailed description of the invention
Whenever used hereinafter, the term "compounds of formula (I)",
Figure imgf000010_0001
or "the present compounds" or similar term is meant to include the compounds of general formula (I), (I*), (la) ,(Ib),(Ic) and (Id), salts, stereoisomeric forms and racemic mixtures or any subgroups thereof.
Compounds for use in the prevention or treatment of an HBV infection in a mammal are disclosed as compounds per se and not limited to this use unless restricted by the claims. The present invention relates to compounds of Formula (I)
Figure imgf000010_0002
B represents a monocyclic 5 to 6 membered aromatic ring, optionally containing one or more heteroatoms each independently selected from the group consisting of O, S and N, such 5 to 6 membered aromatic ring optionally being substituted with one or more substituents each independently selected from the group consisting of hydrogen, halogen, Ci-C3alkyl, CN, CFH2, CF2H and CF3;
Ri represents hydrogen or Ci-C3alkyl;
R2 represents Ci-C6alkyl, Ci-C6alkenyl, Ci-C6alkyl-R5, C(=0)-R5, CFH2, CF2H, CF3, a dihydro-indenyl or tetrahydronaphtalenyl moiety optionally substituted with OH, or a 3-7 membered saturated ring optionally containing one or more heteroatoms each independently selected from the group consisting of O, S and N, such 3-7 membered saturated ring, Ci-C6alkyl-R5 or Ci-C6alkyl optionally being substituted with one or more substituents each independently selected from the group consisting of hydrogen, halogen, Ci-C4alkyloxy, Ci-C4alkyloxycarbonyl, oxo,
C(=0)-Ci-C3alkyl, Ci-C4alkyl, OH, CN, CFH2, CF2H and CF3;
Or Ri and R2 together with the Nitrogen to which they are attached form a 6-10 membered bicyclic or bridged ring or a 5-7 membered saturated ring, such bicyclic, bridged or saturated ring moiety optionally containing one or more additional heteroatoms each independently selected from the group consisting of O, S and N, such 5-7 membered saturated ring optionally being substituted with one or more substituents each independently selected from the group consisting of hydrogen, halogen, Ci-C4alkyloxy, Ci-C4alkyloxycarbonyl, oxo, C(=0)-Ci-C3alkyl,
Ci-C4alkyl, OH, CN, CFH2, CF2H and CF3;
Each R4 is independently selected from hydrogen, halogen, Ci-C4alkyloxy, Ci-C4alkyl, Ci-C4alkenyl, OH, CN, CFH2, CF2H, CF3 , HC≡C or a 3-5 membered saturated ring optionally containing one or more heteroatoms each independently selected from the group consisting of O and N, such Ci-C4alkyl optionally substituted with OH;
R5 represents Ci-C6alkyl, CFH2, CF2H, CF3i phenyl, pyridyl or a 3-7 membered
saturated ring optionally containing one or more heteroatoms each independently selected from the group consisting of O, S and N, such 3-7 membered saturated ring optionally being substituted with one or more substituents each independently selected from the group consisting of hydrogen, halogen, Ci-C4alkyloxy,
Ci-C4alkyloxycarbonyl, oxo, C(=0)-Ci-C3alkyl, Ci-C4alkyl, OH, CN, CFH2, CF2H and CF3;
or a pharmaceutically acceptable salt or a solvate thereof. In a first aspect, the invention further provides compound of Formula (I)
Figure imgf000012_0001
or a stereoisomer or tautomeric form thereof, wherein:
B represents a monocyclic 5 to 6 membered aromatic ring, optionally containing one or more heteroatoms each independently selected from the group consisting of O, S and N, such 5 to 6 membered aromatic ring optionally being substituted with one or more substituents each independently selected from the group consisting of hydrogen, halo, Ci-C3alkyl, CN, CFH2, CF2H and CF3;
Ri represents hydrogen or Ci-C3alkyl;
R2 represents Ci-C6alkyl, Ci-C6alkenyl, Ci-C6alkyl-R5, C(=0)-R5, CFH2, CF2H, CF3, a 2-hydroxy-2,3-dihydro-lH-indenyl moiety or a 3-7 membered saturated ring optionally containing one or more heteroatoms each independently selected from the group consisting of O, S and N, such 3-7 membered saturated ring, Ci-Cealkyl- R5 or Ci-C6alkyl optionally being substituted with one or more substituents each independently selected from the group consisting of hydrogen, halogen, Ci-C4alkyl- oxy, Ci-C4alkyloxycarbonyl, oxo, C(=0)-Ci-C3alkyl, Ci-C4alkyl, OH, CN, CFH2,
CF2H and CF3;
Or Ri and R2 together with the Nitrogen to which they are attached form a l ,4-dioxa-8-azaspiro[4.5]decyl moiety, a 2-oxa-6-azaspiro[3.3]heptyl moiety or a 5-7 membered saturated ring optionally containing one or more additional heteroatoms each independently selected from the group consisting of O, S and N, such 5-7 membered saturated ring optionally being substituted with one or more substituents each independently selected from the group consisting of hydrogen, halogen, Ci-C4alkyloxy, Ci-C4alkyloxycarbonyl, oxo, C(=0)-Ci-C3alkyl,
Ci-C4alkyl, OH, CN, CFH2, CF2H and CF3;
Each R4 is independently selected from hydrogen, halogen, Ci-C4alkyloxy, Ci-C4alkyl, Ci-C4alkenyl, OH, CN, CFH2, CF2H, CF3 , HC≡C or a 3-5 membered saturated ring optionally containing one or more heteroatoms each independently selected from the group consisting of O and N, such Ci-C4alkyl optionally substituted with OH; R5 represents Ci-Cealkyl, CFH2, CF2H, CF3i phenyl, pyridyl or a 3-7 membered saturated ring optionally containing one or more heteroatoms each independently selected from the group consisting of O, S and N, such 3-7 membered saturated ring optionally being substituted with one or more substituents each independently selected from the group consisting of hydrogen, halogen, Ci-C4alkyloxy,
Ci-C4alkyloxycarbonyl, oxo, C(=0)-Ci-C3alkyl, Ci-C4alkyl, OH, CN, CFH2, CF2H and CF3; or a pharmaceutically acceptable salt or a solvate thereof.
In one embodiment, at least one R4 represents Fluor, and one other R4 is selected from the group consisting of Ci-C3alkyl, Ci-C3alkenyl, CHF2 or cyclopropyl.
In a sub-embodiment, one R4 represents Fluor and one other R4 is selected from the group consisting of methyl or CHF2i preferably methyl, and wherein the location of said Fluor is on the para position and the location of said methyl or CHF2 is on the meta position related to the Nitrogen(*) as indicated In Formula (I*) below.
Figure imgf000013_0001
In yet another embodiment, the invention provides compound of Formula (I) wherein at least one R4 represents Fluor, and one other R4 is selected from the group consisting of Ci-C3alkyl, Ci-C3alkenyl, CHF2 or cyclopropyl; more preferably, one R4 represents Fluor and one other R4 is selected from the group consisting of methyl or CHF2 and wherein the location of said Fluor is on the para position and the location of said methyl or CHF2 is on the meta position related to the Nitrogen (*) and R2 represents a 4-7 membered saturated ring containing carbon and one or more oxygen atoms, such 4-7 membered saturated ring optionally being substituted with one or more substituents each independently selected from the group consisting of hydrogen, halo, Ci-C4alkyl- oxy, Ci-C4alkyloxycarbonyl,
Figure imgf000013_0002
Ci-C4alkyl, OH, CN, CFH2, CF2H and CF3.
In yet another embodiment, compounds are disclosed wherein one R4 on the para position represents Fluor and the other one R4 on the meta position represents methyl and such compound is not
Figure imgf000014_0001
In another embodiment of the present invention, compounds according to Formula (I) are provided wherein R2 represents a 4-7 membered saturated ring containing carbon and one or more oxygen atoms, such 4-7 membered saturated ring optionally being substituted with one or more substituents each independently selected from the group consisting of hydrogen, halogen, Ci-C4alkyloxy, Ci-C4alkyloxycarbonyl,
C(=0)-Ci-C3alkyl, Ci-C4alkyl, OH, CN, CFH2, CF2H and CF3. A preferred substituent for such a 4-7 membered saturated ring containing carbon and one or more oxygen atoms is Ci-C4alkyl. In a sub-embodiment, the saturated ring is a 4, 5 or 6 membered ring.
In another embodiment of the present invention, compounds according to Formula (I) are provided wherein R2 represents a 4-7 membered saturated ring containing carbon and one or more nitrogen atoms, such 4-7 membered saturated ring optionally being substituted with one or more substituents each independently selected from the group consisting of hydrogen, halogen, Ci-C4alkyloxy, Ci-C4alkyloxycarbonyl ,
Figure imgf000014_0002
Ci-C4alkyl, OH, CN, CFH2, CF2H and CF3.In a further embodiment, R2 represents a 4-7 membered saturated ring containing carbon and one or more oxygen atoms, such 4-7 membered saturated ring optionally being substituted with one or more substituents each independently selected from the group consisting of hydrogen, halogen, Ci-C4alkyloxy, Ci-C4alkyloxycarbonyl,
Figure imgf000014_0003
Ci-C4alkyl, OH, CN, CFH2, CF2H and CF3 wherein such compound is not
Figure imgf000015_0001
Preferably, any optional substituent on such 3-7, 4-7 and 5-7 membered saturated ring, 6-10 membered bicyclic or bridged ring, Ci-C6alkyl-R5 or Ci-C6alkyl is independently selected from the group consisting of hydrogen, Fluoro, OH, Ci-C3alkyl and CF3, most preferably from the group consisting of hydrigen Ci-C3alkyl, Fluoro and CF3.
In another embodiment of the present invention, compounds according to Formula (I) are provided wherein B represents phenyl or thiophene, optionally being substituted with one or more substituents each independently selected from the group consisting of hydrogen, halogen, Ci-C3alkyl, CN, CFH2, CF2H and CF3.
In one sub-embodiment, compounds according to the present invention are represented by Formula (la)
Figure imgf000015_0002
(la), wherein Rls R2 and R4 are defined as in any one of the embodiments as described. In a sub-embodiment, such compounds are represented by Formula (lb)
Figure imgf000015_0003
wherein Rls R2, R4 are defined as in any one of the embodiments as described and R3 is selected from the group comprising hydrogen, halogen, Ci-C3alkyl, CN, CFH2, CF2H, CF3. In a preferred embodiment, R3 represents Fluor or hydrogen, more preferably hydrogen.
In yet another sub-embodiment, compounds are represented by Formula (Ic):
Figure imgf000016_0001
wherein Rl s R2 and R4 are defined as in any one of the embodiments as described.
In one sub-embodiment, compounds according to the present invention are represented by Formula (Id)
Figure imgf000016_0002
(Id)
wherein Rl s R2 and R4 are defined as in any one of the embodiments described and R3 is selected from the group comprising hydrogen, halogen, Ci-C3alkyl, CN, CFH2, CF2H, CF3. In a preferred embodiment, the compounds according to the invention are envisioned for use in the prevention or treatment of an HBV infection in a mammal.
In one further aspect, the present invention provides compounds which can be represented by Formula (I):
Figure imgf000016_0003
or a stereoisomer or tautomeric form thereof, wherein: B represents a monocyclic 5 to 6 membered aromatic ring, optionally containing one or more heteroatoms each independently selected from the group consisting of O, S and N, such 5 to 6 membered aromatic ring optionally being substituted with one or more substituents each independently selected from the group consisting of hydrogen, halo, Ci-C3alkyl, CN, CFH2, CF2H and CF3;
Ri represents hydrogen or Ci-C3alkyl;
R2 represents Ci-C6alkyl, Ci-C3alkyl-R5, benzyl, C(=0)-R5, CFH2, CF2H, CF3 or a 3-7 membered saturated ring optionally containing one or more heteroatoms each independently selected from the group consisting of O, S and N, such
3-7 membered saturated ring or Ci-Cealkyl optionally being substituted with one or more substituents each independently selected from the group consisting of hydrogen, halo, Ci-C4alkyloxy, oxo, C(=0)-Ci-C3alkyl, Ci-C4alkyl, OH, CN, CFH2, CF2H and CF3;
Or Ri and R2 together with the Nitrogen to which they are attached form a l ,4-dioxa-8-azaspiro[4.5] moiety or a 5-7 membered saturated ring, optionally containing one or more additional heteroatoms each independently selected from the group consisting of O, S and N, such 5-7 membered saturated ring optionally being substituted with one or more substituents each independently selected from the group consisting of hydrogen, halo, Ci-C4alkyloxy, oxo, C(=0)-Ci-C3alkyl, Ci-C4alkyl, OH, CN, CFH2, CF2H and CF3; Each R4 is independently selected from hydrogen, halo, Ci-C4alkyloxy, Ci-C4alkyl, OH, CN, CFH2, CF2H, CF3 , HC≡C or a 3-5 membered saturated ring optionally containing one or more heteroatoms each independently selected from the group consisting of O and N; R5 represents Ci-C6alkyl, CFH2, CF2H, CF3 or a 3-7 membered saturated ring
optionally containing one or more heteroatoms each independently selected from the group consisting of O, S and N, such 3-7 membered saturated ring optionally being substituted with one or more substituents each independently selected from the group consisting of hydrogen, halo, Ci-C4alkyloxy, oxo, C(=0)-Ci-C3alkyl, Ci-C4alkyl, OH, CN, CFH2, CF2H and CF3; or a pharmaceutically acceptable salt or a solvate thereof. These compounds are especially suited for use in the prevention or treatment of an HBV infection in a mammal.
In yet a further aspect, the invention relates to compounds according to Formula (I)
Figure imgf000018_0001
or a stereoisomer or tautomeric form thereof, wherein:
B represents a monocyclic 5 to 6 membered aromatic ring, optionally containing one or more heteroatoms each independently selected from the group consisting of O, S and N, such 5 to 6 membered aromatic ring optionally being substituted with one or more substituents each independently selected from the group consisting of hydrogen, halo, Ci-C3alkyl, CN, CFH2, CF2H and CF3;
Ri represents hydrogen or Ci-C3alkyl;
R2 represents a 4-7 membered saturated ring consisting of carbon atoms and one or more heteroatoms each independently selected from the group consisting of O or S, such 4-7 membered saturated ring optionally being substituted with one or more substituents each independently selected from the group consisting of hydrogen, halo, Ci-C4alkyloxy, oxo, C(=0)-Ci-C3alkyl, Ci-C4alkyl, OH, CN, CFH2, CF2H and CF3;
Each R4 is independently selected from hydrogen, halo, Ci-C4alkyloxy, Ci-C4alkyl, OH, CN, CFH2, CF2H, CF3 , HC≡C or a 3-5 membered saturated ring optionally containing one or more heteroatoms each independently selected from the group consisting of O and N;
or a pharmaceutically acceptable salt or a solvate thereof.
The present invention additionally relates to compound of Formula (I)
Figure imgf000019_0001
or a stereoisomer or tautomeric form thereof, or a pharmaceutically acceptable salt or a solvate thereof
wherein:
B represents a monocyclic 5 to 6 membered aromatic ring, optionally containing one or more heteroatoms each independently selected from the group consisting of O, S and N, such 5 to 6 membered aromatic ring optionally being substituted with one or more substituents each independently selected from the group consisting of hydrogen, halo, Ci-C3alkyl, CN, CFH2, CF2H and CF3;
Ri represents hydrogen or Ci-C3alkyl;
R2 represents Ci-C6alkyl, Ci-C3alkyl-R5, benzyl, C(=0)-R5, CFH2, CF2H, CF3 or a 3-7 membered saturated ring optionally containing one or more heteroatoms each independently selected from the group consisting of O, S and N, such
3-7 membered saturated ring or Ci-Cealkyl optionally being substituted with one or more substituents each independently selected from the group consisting of hydrogen, halo, Ci-C4alkyloxy, oxo, C(=0)-Ci-C3alkyl, Ci-C4alkyl, OH, CN, CFH2, CF2H and CF3;
Or Ri and R2 together with the Nitrogen to which they are attached form a l ,4-dioxa-8-azaspiro[4.5] moiety or a 5-7 membered saturated ring, optionally containing one or more additional heteroatoms each independently selected from the group consisting of O, S and N, such 5-7 membered saturated ring optionally being substituted with one or more substituents each independently selected from the group consisting of hydrogen, halo, Ci-C4alkyloxy, oxo, C(=0)-Ci-C3alkyl, Ci-C4alkyl, OH, CN, CFH2, CF2H and CF3;
Each R4 is independently selected from hydrogen, halo, Ci-C4alkyloxy, Ci-C4alkyl, OH, CN, CFH2, CF2H, CF3 , HC≡C or a 3-5 membered saturated ring optionally containing one or more heteroatoms each independently selected from the group consisting of O and N; R5 represents Ci-Cealkyl, CFH2, CF2H, CF3 or a 3-7 membered saturated ring optionally containing one or more heteroatoms each independently selected from the group consisting of O, S and N, such 3-7 membered saturated ring optionally being substituted with one or more substituents each independently selected from the group consisting of hydrogen, halo, Ci-C4alkyloxy, oxo,
Figure imgf000020_0001
Ci-C4alkyl, OH, CN, CFH2, CF2H and CF3;
One sub-embodiment of the invention provides compounds which can be represented by formula
Figure imgf000020_0002
wherein Rl s R2, B are defined as above and each R4 is independently selected from hydrogen, halo, Ci-C4alkyloxy, Ci-C4alkyl, OH, CN, CFH2, CF2H, CF3 or a 3-5 membered saturated ring optionally containing one or more heteroatoms each independently selected from the group consisting of O and N.
In one embodiment, R2 represents a 3-7 membered saturated ring, containing one or more heteroatoms each independently selected from the group consisting of O, S and N, such 3-7 membered saturated ring optionally being substituted with one or more substituents each independently selected from the group consisting of hydrogen, halo, Ci-C4alkyloxy, oxo,
Figure imgf000020_0003
Ci-C4alkyl, OH, CN, CFH2, CF2H and CF3.
In yet another embodiment, R2 represents a 4-7 membered saturated ring containing carbon and one or more oxygen atoms, such 4-7 membered saturated ring optionally being substituted with one or more substituents each independently selected from the group consisting of hydrogen, halo, Ci-C4alkyloxy, C(=0)- Ci-C3alkyl, Ci-C4alkyl, OH, CN, CFH2, CF2H and CF3.
In another embodiment, Ri and R2 together with the Nitrogen to which they are attached form a 5-7 membered saturated ring, optionally containing one or more additional heteroatoms each independently selected from the group consisting of O, S and N, such 5-7 membered saturated ring optionally being substituted with one or more substituents each independently selected from the group consisting of hydrogen, halo, Ci-C4alkyloxy, oxo, C(=0)-Ci-C3alkyl, Ci-C4alkyl, OH, CN, CFH2, CF2H and CF3. In a preferred embodiment of the invention, B represents phenyl or thiophene, optionally being substituted with one or more substituents each independently selected from the group consisting of hydrogen, halogen, Ci-C3alkyl, CN, CFH2, CF2H and CF3.
In a selection of compounds according to the invention, or compounds for use in the prevention or treatment of an HBV infection in a mammal at least one R4 represents Fluor, Ci-C3alkyl, CHF2 or cyclopropyl. Preferably, at least one R4 represents methyl, /-propyl or cyclopropyl. In another embodiment, one R4 represents methyl, /-propyl or cyclopropyl and the other R4 represents Fluor, or hydrogen. The position of R4 preferably is meta and/or para (position indicated from -N~). One specific embodiment is a compound of Formula (I) wherein one R4 on the para position represents Fluor and the other one R4 on the meta position represents Fluor or methyl (position indicated from -N~).
One sub-embodiment of the invention provides compounds which can be represented by formula
Figure imgf000021_0001
wherein Rl s R2, R4 are defined as above and R3 is selected from the group comprising hydrogen, halo, Ci-C3alkyl, CN, CFH2, CF2H, CF3. In a preferred embodiment, R3 represents Fluor or hydrogen.
The invention further relates to compounds according to Formula (I)
Figure imgf000021_0002
(I) or a stereoisomer or tautomeric form thereof, wherein:
B represents a monocyclic 5 to 6 membered aromatic ring, optionally containing one or more heteroatoms each independently selected from the group consisting of O, S and N, such 5 to 6 membered aromatic ring optionally being substituted with one or more substituents each independently selected from the group consisting of hydrogen, halo, Ci-C3alkyl, CN, CFH2, CF2H and CF3;
Ri represents hydrogen or Ci-C3alkyl; R2 represents Ci-C3alkyl-R6 or a 4-7 membered saturated ring consisting of carbon atoms and one or more heteroatoms each independently selected from the group consisting of O or S, such 4-7 membered saturated ring optionally being substituted with one or more substituents each independently selected from the group consisting of hydrogen, halo, Ci-C4alkyloxy, oxo,
Figure imgf000022_0001
Ci-C4alkyl, OH, CN, CFH2, CF2H and CF3;
Each R4 is independently selected from hydrogen, halo, Ci-C4alkyloxy, Ci-C4alkyl, OH, CN, CFH2, CF2H, CF3 , HC≡C or a 3-5 membered saturated ring optionally containing one or more heteroatoms each independently selected from the group consisting of O and N;
R6 represents a 4-7 membered saturated ring optionally containing one or more
heteroatoms each independently selected from the group consisting of O or S, such 4-7 membered saturated ring optionally being substituted with one or more substituents each independently selected from the group consisting of hydrogen, halo, Ci-C4alkyloxy, oxo,
Figure imgf000022_0002
Ci-C4alkyl, OH, CN, CFH2, CF2H and CF3;
or a pharmaceutically acceptable salt or a solvate thereof.
One sub-embodiment of the invention provides compounds which can be represented by formula (la)
Figure imgf000022_0003
wherein Rl s R2, B are defined as above and each R4 is independently selected from hydrogen, halo, Ci-C4alkyloxy, Ci-C4alkyl, OH, CN, CFH2, CF2H, CF3 or a 3-5 membered saturated ring optionally containing one or more heteroatoms each independently selected from the group consisting of O and N.
In one embodiment, R2 represents Ci-C3alkyl-R6 or a 4-7 membered saturated ring consisting of carbon atoms and one or more heteroatoms each independently selected from the group consisting of O or S, such 4-7 membered saturated ring optionally being substituted with one or more substituents each independently selected from the group consisting of hydrogen, halo, Ci-C4alkyloxy, oxo,
Figure imgf000023_0001
Ci-C4alkyl, OH, CN, CFH2, CF2H and CF3.
In a preferred embodiment for the compounds of the invention, B represents phenyl or thiophene, optionally being substituted with one or more substituents each
independently selected from the group consisting of hydrogen, halogen, Ci-C3alkyl, CN, CFH2, CF2H and CF3.
In a selection of compounds according to the invention at least one R4 represents Fluor, Ci-C3alkyl ,CHF2 or cyclopropyl. Preferably, at least one R4 represents methyl, /-propyl or cyclopropyl. In another embodiment, one P represents methyl, /-propyl or cyclopropyl and the other R4 represents Fluor, or hydrogen. The position of R4 preferably is meta and/or para.
One specific embodiment is a compound of Formula (I) wherein one R4 on the para position represents Fluor and the other one R4 on the meta position represents Fluor or methyl.
One sub-embodiment of the compounds of the invention relates to compounds according Formula (lb)
Figure imgf000023_0002
wherein Ri represents hydrogen or Ci-C3alkyl; R2 represents Ci-C3alkyl-R6 or a 4-7 membered saturated ring consisting of carbon atoms and one or more heteroatoms each independently selected from the group consisting of O or S, such 4-7 membered saturated ring optionally being substituted with one or more substituents each independently selected from the group consisting of hydrogen, halo, Ci-C4alkyloxy, oxo,
Figure imgf000024_0001
Ci-C4alkyl, OH, CN, CFH2, CF2H and CF3;
Each R4 is independently selected from hydrogen, halo, Ci-C4alkyloxy, Ci-C4alkyl, OH, CN, CFH2, CF2H, CF3 or a 3-5 membered saturated ring optionally containing one or more heteroatoms each independently selected from the group consisting of O and N;
Re represents a 4-7 membered saturated ring optionally containing one or more
heteroatoms each independently selected from the group consisting of O or S, such
4-7 membered saturated ring optionally being substituted with one or more substituents each independently selected from the group consisting of hydrogen, halo, Ci-C4alkyloxy, oxo,
Figure imgf000024_0002
Ci-C4alkyl, OH, CN, CFH2, CF2H and CF3;
R3 is selected from the group comprising hydrogen, halo, Ci-C3alkyl, CN, CFH2, CF2H, CF3. In a preferred embodiment, R3 represents Fluor or hydrogen.
In one embodiment, R^ represents a 4-7 membered saturated ring consisting of carbon atoms and one or more heteroatoms each independently selected from the group consisting of O or S, such 4-7 membered saturated ring optionally being substituted with one or more substituents each independently selected from the group consisting of hydrogen, halo, Ci-C4alkyloxy, oxo,
Figure imgf000024_0003
Ci-C4alkyl, OH, CN, CFH2, CF2H and CF3.
Further combinations of any of the sub- or preferred embodiments are also envisioned to be in the scope of the present invention.
Preferred compounds according to the invention are compounds or a stereoisomer or tautomeric form thereof with a formula or reference to a formula selected from the following tables 1 and 2: Table 2.
Figure imgf000025_0001
or a pharmaceutically acceptable salt or a solvate thereof
In a further aspect, the present invention concerns a pharmaceutical composition comprising a therapeutically or prophylactically effective amount of a compound of Formula (I) as specified herein, and a pharmaceutically acceptable carrier. A prophylactically effective amount in this context is an amount sufficient to prevent HBV infection in subjects being at risk of being infected. A therapeutically effective amount in this context is an amount sufficient to stabilize HBV infection, to reduce HBV infection, or to eradicate HBV infection, in infected subjects. In still a further aspect, this invention relates to a process of preparing a pharmaceutical composition as specified herein, which comprises intimately mixing a pharmaceutically acceptable carrier with a therapeutically or prophylactically effective amount of a compound of Formula (I), as specified herein.
Therefore, the compounds of the present invention or any subgroup thereof may be formulated into various pharmaceutical forms for administration purposes. As appropriate compositions there may be cited all compositions usually employed for systemically administering drugs. To prepare the pharmaceutical compositions of this invention, an effective amount of the particular compound, optionally in addition salt form, as the active ingredient is combined in intimate admixture with a pharma- ceutically acceptable carrier, which carrier may take a wide variety of forms depending on the form of preparation desired for administration. These pharmaceutical compositions are desirable in unitary dosage form suitable, particularly, for
administration orally, rectally, percutaneously, or by parenteral injection. For example, in preparing the compositions in oral dosage form, 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, 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 employed. For parenteral compositions, the carrier will usually comprise sterile water, at least in large part, though other ingredients, for example, to aid solubility, may be included. Injectable solutions, for example, may be prepared in which the carrier comprises saline solution, glucose solution or a mixture of saline and glucose solution. Injectable suspensions may also be prepared in which case appropriate liquid carriers, suspending agents and the like may be employed. Also included are solid form preparations intended to be converted, shortly before use, to liquid form preparations. In the compositions suitable for percutaneous administration, 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. The compounds of the present invention may also be administered via oral inhalation or insufflation in the form of a solution, a suspension or a dry powder using any art-known delivery system. It is especially advantageous to formulate the aforementioned pharmaceutical compositions in unit dosage form for ease of administration and uniformity of dosage. Unit dosage form as used herein 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
pharmaceutical carrier. Examples of such unit dosage forms are tablets (including scored or coated tablets), capsules, pills, suppositories, powder packets, wafers, injectable solutions or suspensions and the like, and segregated multiples thereof.
The compounds of Formula (I) are active as inhibitors of the HBV replication cycle and can be used in the treatment and prophylaxis of HBV infection or diseases associated with HBV. The latter include progressive liver fibrosis, inflammation and necrosis leading to cirrhosis, end-stage liver disease, and hepatocellular carcinoma.
Due to their antiviral properties, particularly their anti-HBV properties, the compounds of Formula (I) or any subgroup thereof, are useful in the inhibition of the HBV replication cycle, in particular in the treatment of warm-blooded animals, in particular humans, infected with HBV, and for the prophylaxis of HBV infections. The present invention furthermore relates to a method of treating a warm-blooded animal, in particular human, infected by HBV, or being at risk of infection by HBV, said method comprising the administration of a therapeutically effective amount of a compound of Formula (I). The compounds of Formula (I), as specified herein, may therefore be used as a medicine, in particular as medicine to treat or prevent HBV infection. Said use as a medicine or method of treatment comprises the systemic administration to HBV infected subjects or to subjects susceptible to HBV infection of an amount effective to combat the conditions associated with HBV infection or an amount effective to prevent HBV infection.
The present invention also relates to the use of the present compounds in the manufacture of a medicament for the treatment or the prevention of HBV infection. In general it is contemplated that an antiviral effective daily amount would be from about 0.01 to about 50 mg/kg, or about 0.01 to about 30 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 about 1 to about 500 mg, or about 1 to about 300 mg, or about 1 to about 100 mg, or about 2 to about 50 mg of active ingredient per unit dosage form.
The present invention also concerns combinations of a compound of Formula (I) or any subgroup thereof, as specified herein with other anti-HBV agents. The term "combination" may relate to a product or kit containing (a) a compound of Formula (I), as specified above, and (b) at least one other compound capable of treating HBV infection (herein designated as anti-HBV agent), as a combined preparation for simultaneous, separate or sequential use in treatment of HBV infections. In an embodiment, the invention concerns combination of a compound of Formula (I) or any subgroup thereof with at least one anti-HBV agent. In a particular embodiment, the invention concerns combination of a compound of formula (I) or any subgroup thereof with at least two anti-HBV agents. In a particular embodiment, the invention concerns combination of a compound of formula (I) or any subgroup thereof with at least three anti-HBV agents. In a particular embodiment, the invention concerns combination of a compound of formula (I) or any subgroup thereof with at least four anti-HBV agents.
The combination of previously known anti-HBV agents, such as interferon-a (IFN-a), pegylated interferon-a, 3TC, adefovir or a combination thereof, and, a compound of formula (I) or any subgroup thereof can be used as a medicine in a combination therapy.
Generic synthesis: Compound according to Formula (I) can be synthesized as described in general schemes 1 to 7.
A carboxylic acid chloride of general Formula II can be selectively reacted with an aniline of general formula III, for example in an organic solvent like CH2CI2 in the presence of an organic base like triethylamine or DIPEA (N,N-diisopropylethylamine), or, as another example, by addition of the aniline III to a refluxing toluene solution of compound II, resulting in compound IV. The remaining sulfonic acid chloride functionality in compound IV is further reacted with an amine of general formula V, resulting in a compound of general Formula (I). Alternatively a compound of general Formula (I) might be obtained as described in scheme 2. This time the sulfonic acid chloride VI is reacted with an amine of general formula V, for example in an organic solvent like CH2CI2 in the presence of an organic base like triethylamine or DIPEA or or, as another example, in the presence of Na2C03 in a mixture of H2O/THF. The formed compound VII is coupled with aniline of general formula III in the presence of an activating reagent like for example HATU and an organic base like triethylamine or DIPEA.
Figure imgf000029_0001
I
Scheme 1
Figure imgf000029_0002
I
Scheme 2
A general synthesis of compounds of formula IX and X is described in scheme 3. Intermediate IV is reacted with ammonia, resulting in a compound of formula VIII. This intermediate can be further transformed to a compound of formula IX by reacting with a carbonyl chloride, for example cyclohexane carbonyl chloride in the presence of SiC"2 and H2SO4 at reflux in CHCI3. The compound of general formula IX can be further transformed to a compound of formula X. In case Ri equals Me, this can be done by reacting IX with TMSCHN2 in MeOH/CH2Cl2
Figure imgf000030_0001
IX
Scheme 3
In another example, compound IV can be reacted with an amino acid XI, in the presence of a base like NaOH, resulting in compound XII as described in scheme 4. This intermediate XII can then optionally be cyclised to compound XIII for example by heating with acetic anhydride and KOAc in toluene, or converting the carboxylic acid to an acid chloride followed by cyclisation in the presence of a base like triethylamine. Suitable examples of amino acids of structure XI are derivatives of 5-aminopentanoic acid or 4-aminobutanoic acid
Figure imgf000030_0002
Scheme 4
Figure imgf000031_0001
Scheme 5 A synthetic route to compounds of general formula XVI is described in Scheme 5. A aminoethanol derivative XIV, prepared as described in scheme 1 for the compounds of general Formula (I), is transformed in a aziridine derivative XV by treatement with Diethyl diazene-l,2-dicarboxylate and PPh3 in THF. The aziridine of general formula XV is reacted with a nucleophile Nu, resulting in a compound of general formula XVI. Examples of such nucleophiles (Nu) are, but are not limited to, morpholine and 1-methylpiperazine. Examples of a compound synthesized according to the route described in scheme 5, are compounds 116 and 117.
Figure imgf000031_0002
Scheme 6
An alternative method for the synthesis of compounds of general formula VII, is via ester XVII as described in scheme 6. Reaction of XVII with amine V, for example in an organic solvent like CH2CI2 or THF in the presence of an organic base like for example triethylamine or DIPEA, followed by hydrolysis of the ester, for example with LiOH in THF/H20, followed by acidification, results in a compound of general formula VII. A compound of general formula VII, obtained via the route in scheme 2 or scheme 6, can be transformed to and acid chloride of formula XIX, for example by treatement with oxalyl chloride or thionyl chloride. A compound of general formula XIX can then be transformed to a compound of general Formula (I) by reaction with an aniline of general formula III.
A compound of general formula VI can be converted to a compound of general formula II, for example by treatement with oxalyl chloride in CH2CI2.
o
(CrC3alkyl)— O B'
XXI I
(CrC3alkyl)-0
Figure imgf000032_0001
XX
XXV
Figure imgf000032_0002
O
HO^B
XXI I I
Scheme 7 Possible synthetic routes, for compounds of general formula XVII or VI are described in scheme 7, and further exemplified in the experimental section. Chlorosulfonation of carboxylic acids XXI or carboxylic esters XX, can results in compounds of general formula VI or XVII respectively, for example by treatement with chlorosulfonic acid (for example as reviewed in Phosphorus, Sulfur, and Silicon and the Related Elements Vol. 56, Iss. 1-4, 1991). Alternatively, compounds of general formula XXV or XXIV, may be converted to compound of general formula XVII and VI respectively, by conversion to the corresponding diazonium salts (for example by NaN02/HCl), followed by conversion of the diazonium salt to a sulfonyl chloride (for example by S02/CuCl)(for example as described in Organic Process Research & Development, 13(5), 875-879; 2009). Alternatively, compounds of general formula XXII and XXIII (with P 7 equaling H, benzyl or methyl) may be converted to compound of general formula XVII and VI respectively, for example by treatement with Cl2 or N- Chlorosuccinimide in AcOH/H20.
The subsitutents represented by R4 in this general synthesis section are meant to include any substituent or reactive species that is suitable for transformation into any R4 subsitutent according to the present invention without undue burden for the person skilled in the art.
Compounds not specifically described in the synthesis of compounds section below can be sysnthesized according to the Schemes 1-7 above and were commercially acquired.
Synthesis of compounds:
LC-MS methods:
Method A: mobile phase A : H20 (0.1%TFA; B:CH3CN (0.05% TFA) Stop Time : 10 min; gradient time(min) [%A/%B] 0.0 [100/0] to 1 [100/0] to 5 [40/60] to 7.5
[40/60] to 8.0 [100/0]; flow: 0.8 mL/min; column temp.: 50°C, YMC-PACK ODS-AQ, 50x2.0mm 5μιη
Method B: mobile phase A : H20 (0.1%TFA; B:CH3CN (0.05% TFA) Stop Time : 10 min; gradient time(min) [%A/%B] 0.0 [90/10] to 0.8 [90/10] to 4.5 [20/80] to 7.5 [20/80] to 8.0 [90/10]; flow: 0.8 mL/min; column temp.: 50°C, YMC-PACK ODS-AQ, 50x2.0mm 5μιη
Method C: mobile phase A : H20 (0.1 % TFA); B:CH3CN (0.05 % TFA) Stop Time : 10 min; gradient time(min) [%A/%B] 0.0 [90/10] to 0.8 [90/10] to 4.5 [20/80] to 7.5 [20/80]; 9.5 [90/10] flow: 0.8 mL/min; column temp.: 50°C; Agilent TC-C18, 50x2. lmm, 5μιη
Method D: mobile phase A : H20 (0.05 % NH3.H20 ); B: CH3CN Stop Time : 10 min; gradient time(min) [%A/%B] 0.0 [100/0] to 1 [100/0] to 5 [40/60] to 7.5 [40/60]; 8 [100/0] flow: 0.8 mL/min; column temp.: 40 °C, XBridge Shield-RP18, 50*2. lmm 5μιη
Method E: mobile phase A : H20 (0.1%TFA; B:CH3CN (0.05% TFA) Stop Time : 10 min; Post Time: 0.5 min; gradient time(min) [%A/%B]0 [100/0] to 1 [100/0] to 5 [40/60] to 7.5 [15/85] to 9.5 [100/0]; flow: 0.8 mL/min; column temp.: 50°C, Agilent TC-C18, 50x2.1mm, 5μιη
Method F: The LC measurement was performed using an Acquity UPLC (Waters) system with column heater (set at 55 °C). Reversed phase UPLC (Ultra Performance Liquid Chromatography) was carried out on a bridged ethylsiloxane/silica hybrid (BEH) C18 column (1.7 μιη, 2.1 x 50 mm; Waters Acquity) with a flow rate of 0.8 mL/min. Two mobile phases (10 mM ammonium acetate in H20/acetonitrile 95/5; mobile phase B: acetonitrile) were used to run a gradient condition from 95 % A and 5 % B to 5 % A and 95 % B in 1.3 minutes and hold for 0.3 minutes. An injection volume of 0.5 μΐ was used. Cone voltage was 10 V for positive ionization mode and 20 V for negative ionization mode.
Method G: The LC measurement was performed using an Acquity UPLC (Waters) with column heater (set at 55 °C). Reversed phase UPLC (Ultra Performance Liquid
Chromatography) was carried out on a Acquity UPLC HSS T3 column (1.8 μιη, 2.1 x 100 mm; Waters Acquity) with a flow rate of 0.8 mL/min. Two mobile phases (A: 10 mM ammonium acetate in H20/acetonitrile 95/5; mobile phase B: acetonitrile) were used to run a gradient condition from 100 % A and 0 % B to 5 % A and 95 % B in 2.1 minutes and subsequently to 0 % A and 100 % B in 0.9 minutes to 5% A and 95% B in 0.5 min. An injection volume of 1 μΐ was used. Cone voltage was 30 V for positive ionization mode and 30 V for negative ionization mode.
Method H: Reversed phase HPLC was carried out on an Atlantis CI 8 column (3.5 μιη, 4.6 x 100 mm) with a flow rate of 1.6 mL/min. Column heater was set at 45 °C. Two mobile phases (mobile phase A: 70 % methanol + 30 % H20; mobile phase B: 0.1 % formic acid in H20/methanol 95/5) were employed to run a gradient condition from 100 % B to 5 % B + 95 % A in 9 minutes and hold these conditions for 3 minutes. An injection volume of 10 μΐ was used. Cone voltage was 10 V for positive ionization mode and 20 V for negative ionization mode.
Compounds 21, 49-55, 57-62 were purchased from Aurora Fine Chemicals.
Figure imgf000034_0001
Compound 1 3-(chlorosulfonyl)benzoyl chloride (207 mg, 1 mmol) was dissolved in dichloromethane (3 mL) and 4-fluoroaniline (111 mg, 1.0 mmol) and triethylamine (112 mg, l .Ommol) in dichloromethane (2 mL) were added to the mixture at 0°C. The mixture was next stirred at 20°C for 1 hour. To this reaction mixture containing 3-(4-fluoro- phenylcarbamoyl)benzene-l-sulfonyl chloride at 0°C, a solution of triethylamine (121 mg, 1.2 mmol) and 4-aminotetrahydropyran (88 mg, 0.861 mmol) in dichloromethane (3 mL) was added. The mixture was stirred at 20°C for 1 hour. The solvent was removed in vacuo. The residue was purified by high performance liquid chromatography (Column: Phenomenex Synergi C18 150*20mm*5um. A:
H2O+0.1%TFA; B: MeCN). The product fractions were collected and the organic solvent was evaporated. The fraction was neutralized by saturated NaHCOs. The mixture was extracted with dichloromethane. The organic layer was dried over Na2S04 and concentrated resulting in compound 1 (85.4 mg) Method A; Rt: 4.88 min. m/z : 379.2 (M+H)+ Exact mass: 378.1
Following compounds were prepared similarly as compound 1 using the corresponding
Figure imgf000035_0001
Method B; Rt: 4.27 min. m/z : 363.1 (M+H) Exact mass: 362
Compound 3
Figure imgf000035_0002
Method A; Rt: 4.64 min. m/z : 351.1 (M+H) Exact mass: 350.1
Compound 4
Figure imgf000035_0003
Method A; Rt: 4.87 min. m/z : 365.1 (M+H) Exact mass: 364.1 Compound 5
Figure imgf000036_0001
Method A; Rt: 5.32 min. m/z : 349.1 (M+H) Exact mass: 348.1
Compound 79
Figure imgf000036_0002
Method A; Rt: 5.39 min. m/z : 365.2 (M+H) Exact mass: 364.1
1H NMR (400 MHz, CHLOROFORM- ) δ ppm 8.37 (1 H, t, J=1.5 Hz), 8.16 (1 H, br. s.), 8.11 (1 H, dm, J=8.0 Hz), 8.05 (1 H, dm, J=8.0 Hz), 7.57 - 7.70 (3 H, m), 7.08 (2 H, t, J=8.7 Hz), 4.78 (1 H, s), 1.55 (2 H, q, J=7.5 Hz), 1.18 (6 H, s), 0.84 (3 H, t, J=7.5 Hz).
Figure imgf000036_0003
Method A; Rt: 4.20 min. m/z : 415.0 (M+Na) Exact mass: 392.1;
Purified by silica gel chromatography (gradient eluent: petroleum ether/ethyl acetate from 100/1 to 1/1). 1H NMR (400 MHz, DMSO-dg) δ ppm 10.57 (1 H, br. s), 8.33 - 8.47 (1 H, m), 8.19 (1 H, dm, J=7.5 Hz), 8.06 (1 H, dm, J=7.5 Hz), 7.72 - 7.85 (3 H, m), 7.66 - 7.73 (1 H, br. s), 7.12 - 7.31 (2 H, m), 3.42 - 3.58 (4 H, m), 1.71 - 1.92 (2 H, m), 1.27 - 1.50 (2 H, m), 1.06 (3 H, s).
Compound 87
Figure imgf000036_0004
Method B; Rt: 3.94 min. m z : 363.1 (M+H) Exact mass: 362.1
Purified by high performance liquid chromatography over RP-18 (eluent: CH3CN in water (0.1%TFA) from 25 to 55, v/v). 1H NMR (400 MHz, DMSO-dg), δ ppm 0.34- 0.42 (m, 2 H), 0.46-0.54 (m, 2H), 0.75(t, j=7.3 Hz, 3 H), 1.28 (q, J=7.3 Hz, 2 H), 7.15- 7.25 (m,2 H) 7.67-7.83 (m, 3 H), 7.97 (d, J=8.3 Hz; 1 H), 8.14-8.25 (m, 2 H), 8.33 (s, 1 H), 10.55 (s, 1 H). Compound
Figure imgf000037_0001
Method E; Rt: 4.83 min. m/z : 379.1 (M+H)+ Exact mass: 378.1; 1H NMR (400 MHz, DMSO-d6), δ ppm 10.60 (s, 1H), 8.48 (br. s., 1H), 8.39 (s, 1H), 8.23 (d, J=7.8 Hz, 1 H), 8.04 (d, J=7.8 Hz, 1 H), 7.74-7.87 (m, 3 H), 7.23 (t, J=9.0 Hz, 2 H), 4.5 l(d, J= 6.5 Hz, 2 H), 4.20(d, J=6.5 Hz, 2 H), 1.84 (q, J=7.3 Hz, 2 H), 0.64(t, J=7.3 Hz, 3 H). Prepared similarly as described for compound 1, using 3-ethyloxetan-3-amine instead of 4-aminotetrahydropyran. Synthesis of 3-ethyloxetan-3-amine: 3-ethyloxetane-3- carboxylic acid (3.0g, 23.1 mmol), DPPA (Diphenylphosphoryl azide, 7.61 g,
27.7 mmol), triethylamine (3.0 g, 23.1 mmol) and BnOH (2.99 g, 27.7 mmol) were dissolved in toluene (50 mL). The mixture was stirred at 110°C overnight. The solvent was removed in vacuo. Dichloromethane (50 mL) was added. The mixture was washed with IN HC1 (20 mL). The aqueous layer was extracted with dichloromethane (20 mL). The combined organic layers were washed with brine and dried over Na2S04. The solvent was removed in vacuo. The residue was purified by column chromatography over silica gel (eluent: petroleum ether / ethyl acetate from 100/1 to 60/40) resulting in benzyl 3-ethyloxetan-3-ylcarbamate (4.0 g). To a solution of benzyl 3-ethyloxetan-3-yl- carbamate (2.0g, 8.5mmol) and cyclohexa-1, 4-diene (1.02 g, 12.75 mmol) in MeOH (20 mL) was added Pd-C (10%, 0.2 g) under N2. The mixture was stirred under H2 balloon at 25°C for 4 hours. After filtration, the filtrate was concentrated resulting in 3-ethyloxetan-3-amine (860 mg), which was used as such in the next reaction.
Synthesis of compound 6:
Figure imgf000037_0002
Compound 6 To a solution of 3-(chlorosulfonyl)benzoic acid (1 g, 4.53 mmol) in CH2C12 (20 mL) at 5°C, cyclohexanamine (0.899 g, 9.06 mmol) and triethylamine (1.38 g, 13.60 mmol) were successively added drop wise. The solution was stirred at room temperature overnight. The mixture was washed with IN HC1 (50 mL). The organic phase was dried over MgS04 and concentrated resulting in 3-(N-cyclohexylsulfamoyl)benzoic acid as a white solid (1.2 g), which was used in the next step without purification. To a solution of 3-(N-cyclohexylsulfamoyl)benzoic acid (1.2 g, 4.24 mmol) in DMF (15 mL) at 5°C, 4-fluoroaniline (0.52 g, 4.66 mmol) and DIPEA (1.64 g, 12.71 mmol) were successively added.. The mixture was stirred for 20 minutes and then HATU (1.93 g, 5.08 mmol) was added. The solution was stirred at room temperature overnight. To the reaction mixture aqueous NaHC03 (50 mL) was added followed by EtOAc (50 mL). The organic layer washed with HC1 (5%; 50 mL) and brine. The organic layer was dried with MgS04 and concentrated, resulting in a residue. The obtained residue was purified by a silica gel chromatography column (Petroleum ether: EtOAc=2: l) resulting in compound 6 as a white solid (850 mg). Method B; Rt: 4.50 min. m/z : 377.2 (M+H)+ Exact mass: 376.1
Synthesis of compound 7
Figure imgf000038_0001
Compound 7
To 5-(chlorosulfonyl)-2-fluorobenzoic acid (10 g, 41.91 mmol) in EtOAc (150 mL) cyclohexanamine (12.47 g, 125.72 mmol) was added at room temperature. The reaction mixture was stirred at room temperature for 10 minutes and washed with IN HC1 (100 mL). The organic phase was dried over MgS04 and concentrated resulting in 5-(N-cyclohexylsulfamoyl)-2-fluorobenzoic acid as a white solid (10.9 g), which was used in the next steps without further purification. To a solution of 5-(N-cyclohexyl- sulfamoyl)-2-fluorobenzoic acid (1 g, 3.32 mmol) in DMF (15 mL) 3-(trifluoromethyl)- aniline (0.54 g, 3.32 mmol) and DIPEA (1.29 g, 9.96 mmol) were successively added at 5°C. The mixture was stirred for 20 minutes and then HATU (1.51 g, 3.98 mmol) was added. The solution was stirred at room temperature overnight. To the reaction mixture aqueous NaHC03 (50 mL), was added followed by EtOAc (50 mL). The organic layer was washed with HC1 (5%) and brine. The organic layer was dried with MgS04, concentrated in vacuo, and the obtained residue was purified by preparative HPLC resulting in compound 7 (902 mg) as a white solid. Method B; Rt: 4.85 min. m/z : 445.2 (M+H)+ Exact mass: 444.1; 1H NMR (400 MHz, DMSO-d6) δ ppm 10.94 (1 H, br. s), 8.15 - 8.22 (1 H, m), 8.12 (1 H, dd, J=6.5, 2.5 Hz), 8.03 (1 H, ddd, J=9.0, 4.5, 2.5 Hz), 7.88 - 7.97 (1 H, m), 7.83 (1 H, d, J=7.5 Hz), 7.58 - 7.67 (2 H, m), 7.46 - 7.54 (1 H, m), 2.90 - 3.07 (1 H, m), 1.51 - 1.67 (4 H, m), 1.38 - 1.51 (1 H, m), 0.96 - 1.27 (5 H, m)
Examples of compounds prepared similar as compound 7, using the corresponding anilines instead of 3-(trifluoromethyl)aniline: Compound 18
Figure imgf000039_0001
1H NMR (400 MHz, DMSO-d6) δ ppm 10.68 (1 H, br. s), 8.08 (1 H, dd, J=6.0, 2.5 Hz), 8.01 (1 H, ddd, J= 8.5, 4.5, 2.5 Hz), 7.83 (1 H, br. s), 7.70 - 7.77 (2 H, m), 7.60 (1 H, app. t, J= 9.0 Hz), 7.18 - 7.27 (2H, m), 2.90 - 3.07 (1 H, m), 1.53 - 1.67 (4 H, m), 1.40 - 1.53 (1 H, m), 0.96 - 1.25 (5 H, m). Method C; Rt: 4.21 min. m/z : 395.1 (M+H)+ Exact mass: 394.1
Compound 19
Figure imgf000039_0002
Method C; Rt: 4.17 min. m/z : 377.1 (M+H) Exact mass Compound 43
Figure imgf000039_0003
Method C; Rt: 4.53 min. m z : 41 1.1 (M+H) Exact mass: 410.1
Figure imgf000039_0004
Compound 8
To a solution of (i?)-tetrahydrofuran-3 -amine (0.87 g, 9.97 mmol) in THF (20 mL) aqueous sodium hydroxide was added (4 mL, 5 N) in ice bath followed by 3-(chloro- sulfonyl)benzoic acid (2.2 g, 9.97 mmol). After stirring at 25°C for 3 hours, the reaction mixture was diluted with H20 (20 mL) and extracted with EtOAc (20 mL). The aqueous layer was adjusted to pH=3 by aq. HC1 (2 N) and then the resulting mixture was extracted with EtOAc (3 x 20 mL). The combined organic layer was washed by brine, dried over anhydrous MgS04 and concentrated in vacuo resulting in compound (i?)-3-(N-(tetrahydrofuran-3-yl)sulfamoyl)benzoic acid (900 mg). To a solution of compound (i?)-3-(N-(tetrahydrofuran-3-yl)sulfamoyl)benzoic acid (0.80 g, 2.95 mmol), 4-fluoroaniline (0.39g, 3.54 mmol), and HATU (3.36 g, 8.85 mmol) in CH2CI2 (10 mL) cooled in an ice bath under N2 atmosphere,DIPEA (0.57g, 0.44 mmol) was added. The resulting mixture was diluted with CH2C12 (15 mL) and washed with saturated aqueous NaHC03 (15 mL) and brine (10 mL). After drying over anhydrous MgS04 the solvent was removed in vacuo. The obtained residue was purified by preparative high performance liquid chromatography over RP-18 (eluent: CH3CN in H20: from 40% to 80%, v/v; 0.05%> TFA as addition). The pure fractions were collected and the volatiles were removed in vacuo. The aqueous layer was adjusted to PH=7 with Amberlite IRA-900 ion exchange resin (OH form), filtrated and lyophilized. The obtained residue was further purified by prep. SFC (Column:Chiralpak AD-3 150x4.6mm I.D., 3um Mobile phase: 40% of methanol (0.05% diethylamine) in C02. Flow rate: 2.5 mL/min) resulting in compound 8 (370 mg) Method A; Rt: 4.6 min. m/z
: 365.2 (M+H)+ Exact mass: 364.1; [«]"= - 13.60 (c=0.11, MeOH) 1H NMR
(400 MHz, DMSO- g) δ ppm 10.57 (1 H, br. s), 8.34 - 8.40 (1 H, m), 8.18 - 8.27 (1 H, m), 8.09 (1 H, br. s), 7.99 - 8.06 (1 H, m), 7.74 - 7.84 (3 H, m), 7.13 - 7.33 (2 H, m), 3.64 - 3.83 (2 H, m), 3.50 - 3.64 (2 H, m), 3.35 - 3.39 (1 H, m), 1.80 - 1.99 (1 H, m), 1.51 - 1.68 (1 H, m).
Figure imgf000040_0001
To an iced-cooled mixture of (5)-tetrahydrofuran-3 -amine hydrochloride (0.500 g, 4.41 mmol) and NaOH (0.485 g, 12.138 mmol) in H20 (5 mL) and THF (5 mL) 3-(chlorosulfonyl)benzoic acid (0.893 g, 4.406 mmol) was added in several portions. Then, the reaction mixture was stirred at 20°C for 2 hours. The resulting mixture was diluted with H20 (10 mL) and extracted with ethyl acetate (10 mL). The pH value of aqueous layer was adjusted to 3 by adding IN HC1 and then the mixture was extracted with ethyl acetate (3 x 10 mL). The combined organic layer was washed by brine (10 mL), dried over anhydrous Na2S04 and concentrated under reduced pressure resulting in (5)-3-(N-(tetrahydrofuran-3-yl)sulfamoyl)benzoic acid (0.60 g). To an ice cooled mixture of (5)-3-(N-(tetrahydrofuran-3-yl)sulfamoyl)benzoic acid (600 mg, 2.212 mmol), 4-fluoroaniline (270 mg, 2.433mmol) and HATU (1.01 g, 2.654 mmol) in DMF (5 mL) DIPEA (1.15 mL, 6.636 mmol) was added under N2 atmosphere. The resulting mixture was stirred at 20°C for 2 hour. The solvent was removed in vacuo. The mixture was washed with saturated aqueous critic acid (10 mL), brine and dried over Na2S04. The solvent was removed in vacuo. The residue was purified by column chromatography over silica gel (gradient eluent: petroleum ether/ethyl acetate from 100/0 to 10/90). The pure fractions were collected and the solvent was removed in vacuo. The residue was further purified by preparative high performance liquid chromatography over RP-18 (eluent: CH3CN in H20 from 40% to 80%, v/v; 0.06% NH4HC03 as addition). The pure fractions were collected and the volatiles were removed in vacuo. The aqueous layer was lyophilized to dryness resulting in compound 9 (0.48 g) Method A; Rt: 4.6 min. m/z : 365.2 (M+H)+ Exact mass: 364.1;[α]η = +15.56 (c 0.10, MeOH); 1H NMR (400 MHz, 80°C, DMSO-d6) δ ppm 10.35 (1 H, br. s), 8.32 - 8.48 (1 H, m), 8.15 - 8.32 (1 H, m), 8.03 (1 H, br. s), 7.83 - 7.94 (1 H, m), 7.68 - 7.83 (3 H, m), 7.06 - 7.31 (2 H, m), 3.70 - 3.87 (2 H, m), 3.51 - 3.70 (2 H, m), 3.32 - 3.48 (1 H, m), 1.85 - 2.04 (1 H, m), 1.59 - 1.78 (1 H, m) Compounds prepared similarly as described for compound 8 and 9 from the
corresponding amines instead of tetrahydrofuran-3 -amine :
Compound 10
Figure imgf000041_0001
Method B; Rt: 4.24 min. m/z : 365.2 (M+H) Exact mass: 364.1;
Compound 76
Figure imgf000041_0002
Using 1-methylcyclopentanamine instead of tetrahydrofuran-3 -amine, purified using Gemini 250*20mm*5um (eluent: CH3CN in H20 (0.1% TFA) from 40% to 70%, v/v).Method B; Rt: 4.24 min. m/z : 377.2 (M+H)+ Exact mass: 376.1; Synthesis of 3-(N-cyclopentylsulfamoyl)benzoic acid:
To an iced-cooled mixture of cyclopentanamine (1.93 g, 22.66 mmol) and a solution of NaOH (1.81 g, 45.32 mmol) in H20 (25 mL) and THF (25 mL) was added 3-(chloro- sulfonyl)benzoic acid (5.0 g, 22.66 mmol) in portions. The reaction mixture was stirred at 20°C for 2 hours. The resulting mixture was diluted with H20 (20 mL) and extracted with ethyl acetate (30 mL). The aqueous layer was separated and adjusted pH =2 by 4 N HCl and extracted with dichloromethane (3 x 30 mL). The combined organic layer was washed by brine (15 mL), dried over anhydrous Na2S04 and concentrated under reduced pressure to afford 3-(N-cyclopentylsulfamoyl)benzoic acid (4.5 g).
Compound 11
Figure imgf000042_0001
To an ice cooled mixture of 3-(N-cyclopentylsulfamoyl)benzoic acid (250 mg,
0.928 mmol), 4-fiuoro-3-methylaniline (116.2 mg, 0.928 mmol), HATU (388.2 mg, 1.021 mmol) in CH2C12 (15 mL) DIPEA (359.8 mg, 2.784 mmol) was added under a N2 atmosphere. The resulting mixture was stirred at 20°C for 16 hours. The solvent was removed in vacuo. The mixture was washed with saturated aqueous critic acid (10 mL), brine and dried over Na2S04. The solvent was removed in vacuo. The residue was purified by column chromatography over silica gel (gradient eluent: petroleum ether/ethyl acetate from 100/0 to 10/90). The pure fractions were collected and the solvent was removed in vacuo. The residue was further purified by preparative high performance liquid chromatography over RP-18 (eluent: CH3CN in H20 from 45% to 75%), v/v; 0.01%) HCl as addition). The pure fractions were collected and the volatiles were removed in vacuo. The aqueous layer was adjusted to Ph=7 with Amberlite IRA- 900 ion exchange resin (OH form), filtrated and lyophilized to dryness to afford compound 11 (170.0 mg). Method B; Rt: 4.31 min. m/z : 377.2 (M+H)+ Exact mass: 376.1; 1H NMR (400 MHz, DMSC /6) δ ppm 10.47 (1 H, br. s), 8.33-8.35 (1 H, m), 8.17 (1 H, dm, J=8.0), 7.98 (1 H, dm, J=8.0), 7.78 (1 H, d, J=7.0 Hz), 7.74 (1 H, t, J=8.0 Hz), 7.62 - 7.68 (1 H, m), 7.53 - 7.61 (1 H, m), 7.13 (1 H, t, J=9.0 Hz), 3.37 - 3.48 (1 H, m), 2.23 (3 H, d, J=1.8 Hz), 1.44 - 1.69 (4 H, m), 1.12 - 1.45 (4 H, m) Prepared similarly as compound 11 starting from the corresponding anilines instead of 4-fluoro-3-methylaniline :
Compound
Figure imgf000042_0002
1H NMR (400 MHz, DMSC /6) δ ppm 10.60 (1 H, bs), 8.36 (1 H, t, J=1.5 Hz), 8.19 (1 H, dm, J=7.5 Hz), 8.02 (1 H, dm, J=7.5 Hz), 7.81 (1 H, d, J=7.5 Hz), 7.78 (1 H, t, J=7.5 Hz), 7.55 (1 H, dm, J=l 1.0 Hz), 7.38 - 7.46 (1 H, m), 6.82 (1 H, dm, J=9.5 Hz), 3.41 - 3.54 (1 H, m), 2.34 (3 H, s), 1.45 - 1.70 (4 H, m), 1.19 - 1.45 (4 H, m); Method B; Rt: 4.41 min. m/z : 377.2 (M+H)+ Exact mass: 376.1
Compound 13
Figure imgf000043_0001
The residue was purified by column chromatography over silica gel (gradient eluent: petroleum ether/ethyl acetate from 100/0 to 40/60). Method B; Rt: 4.41 min. m/z : 377.2 (M+H)+ Exact mass: 376.1
Compound 14
Figure imgf000043_0002
Method B; Rt: 4.34 min. m/z : 381.2 (M+H) Exact mass: 380.1
1H NMR (400 MHz, DMSO-d6) δ ppm 1.20 - 1.44 (m, 4 H), 1.44 - 1.68 (m, 4 H), 3.44 (sxt, J=6.8 Hz, 1 H), 7.45 (dt, J=10.6, 9.0 Hz, 1 H), 7.51 - 7.60 (m, 1 H), 7.77 (t, J=7.8 Hz, 1 H), 7.80 (d, J=7.2 Hz, 1 H), 7.93 (ddd, J=13.2, 7.5, 2.5 Hz, 1 H), 8.02 (d, J=7.8 Hz, 1 H), 8.19 (d, J=7.7 Hz, 1 H), 8.35 (t, J=1.7 Hz, 1 H), 10.70 (s, 1 H)
Compound 15
Figure imgf000043_0003
Method B; Rt: 4.43 min. m/z : 381.2 (M+H) Exact mass: 380.1
Compound 77
Figure imgf000043_0004
Method B; Rt: 5.45 min. m/z : 363.2 (M+H) Exact mass: 362.1 Compound 81
Figure imgf000044_0001
purified by preparative high performance liquid chromatography (column: Phenomenex Synergi 200mm*77mm, lOum; mobile phase: CH3CN in water (0.1% TFA) from 45% to 75%,). Method A; Rt: 5.87 min. m/z : 413.2 (M+H)+ Exact mass: 412.1
Compound 16
Figure imgf000044_0002
A solution of 3-(N-cyclopentylsulfamoyl)benzoic acid (500 mg, 1.73 mmol) in oxalyl dichloride (10 mL) was stirred at 45°C for 5 hours. The solvent was removed in vacuo. The crude 3-(N-cyclopentylsulfamoyl)benzoyl chloride (600 mg) was used as such in the next step. To an ice cooled mixture of 3-(N-cyclopentylsulfamoyl)benzoyl chloride (600 mg, 1.74 mmol) and 4-amino-2-methylbenzonitrile (230 mg, 1.74 mmol) in
CH2CI2 (5 mL) was added pyridine (10 mL) under N2 atmosphere. The resulting mixture was stirred at 20°C for 16 hours. The solvent was removed in vacuo. The residue was purified by preparative high performance liquid chromatography over RP-18 (eluent: CH3CN in H20 from 50% to 80%, v/v; 0.05% TFA as addition). The pure fractions were collected and the volatiles were removed in vacuo. The aqueous layer was adjusted to PH=7 with Amberlite IRA-900 ion exchange resin (OH form), filtrated and lyophilized resulting in compound 16 (250mg). Method B; Rt: 4.23 min. m/z : 384.2 (M+H)+ Exact mass: 383.1.
Compound 75
Figure imgf000044_0003
Prepared similarly as described for compound 16 using 3-aminobenzonitrile instead of 4-amino-2-methylbenzonitrile. Method A; Rt: 5.24 min. m/z : 370.2 (M+H)+ Exact mass: 369.1. Compound 80
Figure imgf000045_0001
Prepared similarly as described for compound 16 using 4-aminobenzonitrile instead of 4-amino-2-methylbenzonitrile. Method A; Rt: 5.32 min. m/z : 370.2 (M+H)+ Exact mass: 369.1.
Compound 82
Figure imgf000045_0002
Prepared similarly as described for compound 16 using 3-amino-5-methylbenzonitrile instead of 4-amino-2-methylbenzonitrile. Method A; Rt: 5.52 min. m/z : 384.2 (M+H) Exact mass: 383.1.
Compound 17
Figure imgf000045_0003
To a solution of compound 2,4-dichloro-5-(piperidin-l-ylsulfonyl)benzoic acid (1.0 g, 2.96 mmol), m-toluidine (0.38 g, 3.55 mmol), and HATU (1.69 g, 4.44 mmol) in CH2C12 (10 mL) cooled in an ice bath, DIPEA (1.15g, 8.88 mmol) was added under N2 atmosphere. The resulting mixture was diluted with CH2C12 (15 mL) and washed with saturated aqueous NaHC03 (15 mL) and brine (10 mL), dried over anhydrous MgS04 and the solvent was removed in vacuo. The residue was purified by column
chromatography over silica gel (gradient eluent: petroleum ether/ethyl acetate from 100/0 to 40/60). The pure fractions were collected and the solvent was removed in vacuo, resulting in compound 17 (0.65 g). Method B; Rt: 4.70 min. m/z : 427.1 (M+H) Exact mass:426.1
Compound 46
Figure imgf000045_0004
To a solution of 3-(chlorosulfonyl)benzoic acid (1.10 g, 4.97 mmol) in THF (60mL) sodium hydroxide was added (aq., 2 mL, 5N) in ice bath followed by adding N-methyl- cyclopentanamine (0.50 g, 4.97 mmol). After stirring at 25°C for 3 hours, the reaction mixture was diluted with H20 (50mL) and extracted with EtOAc (50mL). The aqueous layer was adjusted to pH=3 by HCl (2N) and extracted with EtOAc (3 x 50mL). The combined organic layer was washed by brine, dried over anhydrous MgSC^ and concentrated in vacuo resulting in 3-(N-cyclopentyl-N-methylsulfamoyl)benzoic acid (0.8 g). To a solution of 3-(N-cyclopentyl-N-methylsulfamoyl)benzoic acid (0.80 g, 2.82 mmol), 4-fluoroaniline (0.31 g, 2.82 mmol), and HATU (1.61 g, 4.24 mmol) in CH2C12 (10 mL), cooled in an icebath, DIPEA (1.09 g, 8.47mmol) was added under N2 atmosphere. The resulting mixture was diluted with CH2C12 (15 mL) and washed with saturated aqueous NaHC03 (15 mL) and brine (10 mL), dried over anhydrous MgSC^ and the solvent was removed in vacuo. The obtained residue was purified by
preparative high performance liquid chromatography over RP-18 (eluent: CH3CN in H20 from 30% to 80%>, v/v; 0.05%> TFA as addition). The pure fractions were collected and the volatiles were removed in vacuo. The aqueous layer was adjusted to Ph=7 with Amberlite IRA-900 ion exchange resin (OH form), filtrated and lyophilized to dryness resulting in compound 46 (0.73g). Method B; Rt: 4.43 min. m/z : 377.2 (M+H)+ Exact mass:376.1
Compound 56
Figure imgf000046_0001
4-fluoroaniline (0.93 g, 8.366 mmol) and DIPEA (2.91 mL, 16.732 mmol) were dissolved in CH2C12 (20 mL). 3-(chlorosulfonyl)benzoyl chloride (2 g, 8.366 mmol) in CH2C12 (20 mL) was added in one portion at 0°C. The mixture was stirred for 1 hour at 0°C. The reaction mixture (40 mL) containing 3-(4-fluorophenylcarbamoyl)benzene-l- sulfonyl chloride was used to the next step without further purification. Ammonia (2.52 g, 18 mmol, 25-28%) wt) was added to a solution of 3-(4-fluorophenylcarbamoyl)- benzene-l-sulfonyl chloride (obtained as above, 6 mmol) in CH2C12 (30 mL) at 0°C. The mixture was stirred for 1 hour at 20°C. 1 N HCl (30 mL) was added to the reaction mixture and the volatiles were partely removed in vacuo. The formed precipitate was filtered and co-evaporated with toluene (10 mL), resulting in N-(4-fluorophenyl)-3- sulfamoylbenzamide (1.6 g). A solution of N-(4-fluorophenyl)-3-sulfamoylbenzamide (1.8 g, 6.12 mmol) and cyclohexanecarbonyl chloride (1.79 g, 12.23 mmol) in chloroform (40 mL) with Si02 (180 mg) and H2SO4 (0.5 mL) was refluxed for 1 hour.
Dichloromethane (20 mL) was added and the solid was filtered off. The filtrate was washed with water (10 mL) and dried over Na2S04. The solvent was removed in vacuo. The obtained residue was purified by silica gel column chromatography (gradient eluent: petroleum ether/ethyl acetate from 100/0 to 70/30). The obtained product (1.2 g, purity 95%) was further washed with methyl t-butyl ether (10 mL) resulting in compound 56 (500 mg, 99.7 % purity). Method A; Rt: 5.51 min. m/z : 405.2 (M+H)+ Exact mass: 404.1; 1H NMR (400 MHz, DMSO-d6) δ ppm 12.16 (1 H, br. s), 10.62 (1 H, br. s), 8.41 (1 H, t, J=2.0 Hz), 8.27 (1 H, dm, J=7.5 Hz), 8.09 (1 H, dm, J=7.5 Hz), 7.73 - 7.82 (3 H, m), 7.07 - 7.33 (2 H, m), 2.11 - 2.31 (1 H, m), 1.43 - 1.80 (5 H, m), 0.94 - 1.32 (5 H, m)
Compound 48
Figure imgf000047_0001
Compound 56 (600 mg) was dissolved in CH2CI2 (6 mL) and MeOH (2 mL) and TMSCHN2 (3.7 mL, 7.415 mmol, 2M in hexane) were added drop wise at 20°C. The mixture was stirred for 2 hours at 20°C. The solvent was removed in vacuo. The residue was purified by flash column (gradient eluent: petroleum ether/ethyl acetate from 100/0 to 70/30) resulting in a residue (0.41 g). The obtained product was further purified by preparative high performance liquid chromatography over RP-18 (eluent: CH3CN in H20 (0.1% TFA) from 20% to 50%, v/v). The pure fractions were collected and the volatiles were removed in vacuo. The precipitate was filtered and the residual water was removed by lyophilization resulting in compound 48 (300 mg). Method B;
Rt: 4.60 min. m/z : 419.2 (M+H)+ Exact mass:418.1; 1H NMR (400 MHz, DMSO-d6) δ ppm 10.62 (1 H, br. s), 8.40 - 8.45 (1 H, m), 8.28 (1 H, dm, J=7.5 Hz), 8.13 (1 H, dm, J=7.5 Hz), 7.66 - 7.95 (3 H, m), 7.07 - 7.33 (2 H, m), 3.40 (3 H, s), 2.73 - 2.92 (1 H, m), 1.42 - 1.77 (5 H, m), 0.90 - 1.35 (5 H, m).
Figure imgf000047_0002
Compound 63
A mixture of ethyl 2-(chlorosulfonyl)-lH-imidazole-4-carboxylate (1 g, 4.19 mmol), Et3N (1.27 g, 12.55 mmol) and cyclohexanamine (0.623 g, 6.28 mmol) in THF (25 mL) was stirred at room temperature for 15 hours. The mixture was concentrated and purified by preparative HPLC (Column: CI 8; Mobile phase A: purified water
(0.075%TFA, V/V); Mobile phase B: acetonitrile; Flow rate: 80mL/min; Gradient: 25-55%, 30 min) resulting in ethyl 2-(N-cyclohexylsulfamoyl)-lH-imidazole-4- carboxylate (0.6 g) as a light yellow solid. To a solution of ethyl 2-(N-cyclohexyl- sulfamoyl)-lH-imidazole-4-carboxylate (0.6 g, 1.99 mmol) in EtOH-H20 (3/1; 20 mL), LiOH (0.145 g, 6.055 mmol) was added. The mixture was stirred at room temperature for 15 hours. The reaction mixture was neutralized with HC1 (2M), diluted with water and then extracted into EtOAc, dried over MgS04, filtered and concentrated resulting in 2-(N-cyclohexylsulfamoyl)-lH-imidazole-4-carboxylic acid (400 mg) as a white solid. A mixture of 2-(N-cyclohexylsulfamoyl)-lH-imidazole-4-carboxylic acid (0.3 g, 1.098 mmol), aniline (0.102 g, 1.098 mmol), DIPEA (0.284 g, 2.196 mmol) and HATU (0.501 g, 1.317 mmol) in DMF (25 mL) was stirred at room temperature for 15 hours. The mixture was purified by preparative HPLC (Column: YMC 150x30mm.
Mobile phase A: purified water (0.075%TFA, V/V); Mobile phase B: acetonitrile; Flow rate: 30mL/min; Gradient: 40-70%, 8 min) resulting in compound 63 (218 mg). Method B; Rt: 3.98 min. m/z : 349.2 (M+H)+ Exact mass:348.1. 1H NMR (400 MHz,
METHANOL-^) δ ppm 1.26 (s, 5 H) 1.51 - 1.62 (m, 1 H) 1.65 - 1.80 (m, 4 H) 3.23 - 3.29 (m, 1 H) 7.10 - 7.18 (m, 1 H) 7.32 - 7.39 (m, 2 H) 7.67-7.74 (m, 2 H) 7.86 (s, 1
Figure imgf000048_0001
Compound 64 A mixture of ethyl 2-(chlorosulfonyl)thiazole-4-carboxylate (3 g, 11.73 mmol), Et3N (3.56 g, 35.2 mmol) and cyclohexanamine (1.75 g, 17.65 mmol) in THF (100 mL) was stirred at room temperature for 15 hours. The mixture was concentrated and purified by preparative HPLC resulting in ethyl 2-(N-cyclohexylsulfamoyl)thiazole-4-carboxylate (2 g) as a white solid. To a solution of ethyl 2-(N-cyclohexylsulfamoyl)thiazole-4- carboxylate (2 g) in EtOH-THF (1/1 , 60 mL) was added LiOH (0.451 g, 18.83 mmol). The mixture was stirred at room temperature for 15 hours. The reaction mixture was neutralized with HC1 (2M), diluted with water and then extracted into EtOAc, dried over MgS04, filtered and concentrated in vacuo, resulting in 2-(N-cyclohexyl- sulfamoyl)thiazole-4-carboxylic acid (1.7 g) as a white solid. A mixture of 2-(N-cyclo- hexylsulfamoyl)thiazole-4-carboxylic acid (1 g), aniline (0.321 g, 3.44 mmol), DIPEA (1.33 g, 10.29 mmol) and HATU (1.57 g, 4.13 mmol) in DMF (40 mL) was stirred at room temperature for 15 hours. The mixture was concentrated and purified by preparative HPLC (Column: SYNERGI 250*50 lOum; Mobile phase A: purified water (0.075%TFA, V/V); Mobile phase B: acetonitrileFlow rate: 80 mL/min Gradient: 35- 65%, 30min) resulting in compound 64 (895 mg) as a white solid. Method B; Rt: 4.45 mm. m/z : 366.1 (M+H)+ Exact mass: 365.1
Compound 65
Figure imgf000049_0001
The mixture of 6-chloro-N-phenylpicolinamide (4 g, 17.19 mmol), phenylmethanethiol (3.23g, 25.79 mmol) and K2C03 (4.75g, 34.38 mmol) in DMF was stirred at 80°C for 18 hour. The reaction mixture was diluted with EtOAc (150 mL), and washed with brine (2 x 200 mL). The organic layer was dried over MgS04, filtered and
concentrated. The residue was purified by flash chromatography on silica gel (20% EtOAc in petroleum ether) to obtain 6-(benzylthio)-N-phenylpicolinamide (2.8 g). N-Chlorosuccinimide (3.42 g, 25.6 mmol) was added to the mixture of 6-(benzylthio)- N-phenylpicolinamide (2 g, 6.24 mmol) in acetic acid (60 mL) and water (40 mL). The reaction mixture was stirred at room temperature for 3 hours. The reaction was diluted with CH2C12 (100 mL). After washing with water, the organic layer was added to the mixture of cyclohexanamine (12.4 g, 125 mmol) and Et3N (50 mL) in CH2C12
(200 mL). The resulting mixture was stirred at room temperature for 4 hours. The reaction mixture was washed with NH4C1 (saturated), brine, dried over MgS04, filtered and concentrated. The obtained residue was purified by preparative HPLC (Column: Synergi 150*30mm*5um; Mobile phase A: purified water (0.075%TFA, V/V); Mobile phase B: acetonitrile; Flow rate: 30mL/min; Gradient: 46-76% (solvent B), 8min) resulting in compound 65 (330 mg). Method B; Rt: 4.46 min. m/z : 360.2 (M+H)+ Exact mass: 359.1. 1H NMR (400 MHz, DMSC /6) δ ppm 1.00 - 1.31 (m, 5 H) 1.34 - 1.47 (m, 1 H) 1.51 - 1.71 (m, 4 H) 3.02 - 3.13 (m, 1 H) 7.15 - 7.21 (m, 1 H) 7.40 - 7.46 (m, 2 H) 7.82 - 7.88 (m, 2 H) 8.15 (dd, J=6.3, 2.5 Hz, 1 H) 8.23 - 8.28 (m, 1 H) 8.29- 8.36 (m, 2 H) 10.47 (s, 1 H)
Compound 66
Figure imgf000049_0002
A mixture of 2-chloro-N-phenylisonicotinamide (2 g, 8.6 mmol), phenylmethanethiol (2.11 g, 17 mmol) and K2C03 (2.35 g, 17 mmol) in DMF was stirred at 80°C for 18 hours. The reaction was diluted with water (200 mL) and extracted with EtOAc (2 x 100 mL). The combined organic layers were washed with brine, dried over MgS04, filtered and concentrated. The obtained residue was purified by silica gel chromatography (0-20 % EtOAc in petroleum ether) resulting in 2-(benzylthio)-N-phenyl- isonicotinamide ( 1 .7 g). N-Ch I orosucc i n i mi do (2.56 g, 19.2 mmol ) was added to a mixture of 2-(benzylthio)-N-phenylisonicotinamide (1.5 g, 4.68 mmol) in acetic acid (20 mL) and water (10 mL). The reaction mixture was stirred at room temperature for 4 hours. The reaction was diluted with CH2CI2 (20 mL). After washing with water, the organic layer was added to the mixture of cyclohexanamine (4.64 lg, 46.8 mmol) and Et3N (10 mL, 71.74 mmol) in CH2CI2 (50mL). The resulting mixture was stirred at room temperature for 4 hours. The reaction mixture was washed with NH4CI
(saturated), brine, dried over MgS04, filtered and concentrated. The obtained residue was purified by preparative HPLC (Column: C18-10um; Mobile phase A: purified water (0.075%TFA, V/V); Mobile phase B: acetonitrile; Flow rate: 80mL/min;
Gradient: 40-70% (solvent B), 25min) resulting in compound 66 (250 mg). Method B; Rt: 4.22 min. m/z: 360.2 (M+H)+ Exact mass: 359.1. 1H NMR (400 MHz, DMSO-d6) δ ppm 0.96 - 1.08 (m, 1 H) 1.08 - 1.24 (m, 4 H) 1.40 - 1.52 (m, 1 H) 1.53 - 1.67 (m, 4 H) 3.11 - 3.22 (m, 1 H) 7.14 - 7.21 (m, 1 H) 7.37 - 7.44 (m, 2 H) 7.78 (d, J=7.8 Hz, 2 H) 7.97 (br. s, 1 H) 8.12 (dd, J=5.0, 1.5 Hz, 1 H) 8.40 (s, 1 H) 8.94 (d, J=5.0 Hz, 1 H) 10.75 (s, 1 H)
Compound 67
Figure imgf000050_0001
2-chloro-N-cyclohexylpyridine-4-sulfonamide (540 mg, 1.965 mmol), PdC^dppf (100 mg, 0.137 mmol) and Et3N (5.89 mmol) in methanol (50 mL) was stirred at 50°C for 18 hours under CO (50Psi) atmosphere. The solvent was removed under reduced pressure. The obtained residue (700 mg) containing methyl 4-(N-cyclohexylsulfamoyl)- picolinate was used in the next step without further purification. K2C03 (421 mg, 3.05mmol) was added to the mixture of methyl 4-(N-cyclohexylsulfamoyl)picolinate in methanol and water. The mixture was stirred at 20°C for 18 hour. The solvent was removed, the residue was diluted with water (50 mL) and washed with EtOAc (2 x 50 mL). The aqueous layer was then acidified to pH = 3 with 1 M HC1 and extracted with EtOAc (2 x 50mL). The combined organic layers were dried over MgS04, filtered and concentrated resulting in 4-(N-cyclohexylsulfamoyl)picolinic acid (380 mg).
HATU (0.76 g, 2.0 mmol) was then added to a mixture of 4-(N-cyclohexylsulfamoyl)- picolinic acid (380 mg, 1.34 mmol), aniline (251 mg, 2.7 mmol) and DIPEA (0.517 g, 4.0 mmol) in DMF (50 mL) at room temperature The resulting mixture was stirred at room temperature for 18 hour. The mixture was diluted with water (200 mL), and extracted with EtOAc. The organic layers were washed with brine, dried over MgS04, filtered and concentrated in vacuo. The obtained residue was purified by silica gel chromatography (10-20% EtOAc in petroleum ether) resulting in compound 67 as a white solid (330 mg). Method B; Rt: 4.58 min. m/z : 360.2 (M+H) Exact mass: 359.1. 1H NMR (300 MHz, DMSO-d6) δ ppm 0.93 - 1.26 (m, 5 H) 1.37 - 1.50 (m, 1 H) 1.50 - 1.69 (m, 4 H) 2.98-3.12 (m, 1 H) 7.15 (t, J=7.2 Hz, 1 H) 7.32-7.45 (m, 2 H) 7.86-7.97 (m, 2 H) 8.03 (dd, J=5.0, 1.5 Hz, 1 H) 8.25 (d, J=7.3 Hz, 1 H) 8.47 (d, J=1.5 Hz, 1 H) 9.00 (d, J=5.0 Hz, 1 H) 10.78 (s, 1 H)
Compound 68
Figure imgf000051_0001
Thionyl chloride (10 mL, 137 mmol) was added drop wise to water (60 mL) at 0-5°C. The mixture was stirred at room temperature for 16 hour. CuCl(40 mg, 0.4 mmol) was added, and the mixture (mixture A) was cooled to -5°C. To a mixture of 5-amino- nicotinic acid in con. HC1 (35 mL), a solution of NaN02 (2.76g, 40 mmol) in of water (40 mL) at -5°C to 0°C, was added (mixture B). The mixture B was added portionwise to the mixture A over 30 minutes, maintaining temperature at -5°C to 0°C.After stirring at 0°C for 1 hour, the solid was collected by filtration, washed with water, and dried in vacuo resulting in 5-(chlorosulfonyl)nicotinic acid (1.05 g). The mixture of
5-(chlorosulfonyl)nicotinic acid (1 g, 4.5 mmol), cyclohexanamine (0.893g, 9 mmol) and Et3N (1.37 mmol, 13.5 mmol) in CH2C12 (30 mL) was stirred at room temperature for 18 hours. The solvent was removed under reduced pressure. The residue was purified by HPLC (Column: C18 lOum; Mobile phase A: purified water (0.075%TFA, V/V); Mobile phase B: acetonitrile; Flow rate: 80mL/min; Gradient: 30-60% (solvent B), 30 min) resulting in 5-(N-cyclohexylsulfamoyl)nicotinic acid as a white solid (1 g). HATU (2.6g, 7mmol) was added to the mixture of 5-(N-cyclohexylsulfamoyl)nicotinic acid (1 g, 3.5 mmol), aniline (391 mg, 4.2 mmol) and DIPEA (1.36 g, 10.5 mmol) in DMF (50 mL) at room temperature The resulting mixture was stirred at room temperature for 18 hour. The mixture was diluted with of water (200 mL) and extracted with EtOAc. The organic layers were washed with brine, dried over MgS04, filtered and concentrated. The residue was purified by silica gel chromatography (10-100%) EtOAc in petroleum ether) resulting in compound 68 (708 mg) as white solid. Method B; Rt: 4.58 min. m/z : 360.2 (M+H)+ Exact mass: 359.1 Compound 69
Figure imgf000052_0001
To an ice-cooled solution of 5-aminopentanoic acid (1.2 g, 3.44 mmol) and IN NaOH (8 mL) in THF (16 mL) was added 3-(4-fluorophenylcarbamoyl)benzene-l-sulfonyl chloride (0.444 g, 3.78mmol). Then the reaction mixture was stirred at 25°C overnight. The resulting mixture was diluted with IN HC1 (10 mL) and extracted with ethyl acetate (2 x 30 mL). The combined organic layers were washed with brine, dried over anhydrous Na2S04 and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (gradient eluent: petroleum ether: ethyl acetate: from 100: 0 to 65:35) resulting in 5-(3-(4-fluorophenylcarbamoyl)phenylsulfonamido) pentanoic acid (0.9 g). A mixture of 5-(3-(4-fluorophenylcarbamoyl)phenylsulfon- amido) pentanoic acid (400 mg, 0.913 mmol), acetic anhydride (0.466 g, 4.57 mmol) and AcOK (1.79 g, 18.3 mmol) in toluene (25 mL) was heated by microwave irradiation at 150°C for 30 minutes. The formed precipitate was filtered off and the filtrate was concentrated in vacuo. The residue was purified by preparative high performance liquid chromatography (eluent: CH3CN in H20 (0.05% HC1) from 0% to 35%, v/v). The pure fractions were collected and adjusted to pH=7 with Amberlite IRA-900(OH)anionic exchange resin. The resin was filtered off and the filtrate was lyophilized to dryness resulting in compound 69 (200 mg). Method A; Rt: 4.97 min. m/z : 377.2 (M+H)+ Exact mass: 376.1; 1H NMR (400 MHz, CHLOROFORM-;/) δ ppm 1.78 - 1.87 (m, 2 H), 1.90 - 1.99 (m, 2 H), 2.44 (t, J=6.8 Hz, 2 H), 3.95 (t, J=6.0 Hz, 2 H), 7.08 (t, J=8.7 Hz, 2 H), 7.55 - 7.70 (m, 3 H), 8.15 (d, J=8.0 Hz, 1 H), 8.20 (d, J=7.8 Hz, 1 H), 8.26 (br. s., 1 H), 8.49 (s, 1 H)
Compound 70
To an iced-cooled mixture of (i?)-butan-2-amine (0.500 g, 6.837 mmol) and NaOH (0.547 g, 13.67 mmol) in H20 (15 mL) and THF (15 mL), 3-(chlorosulfonyl)benzoic acid was added (1.508 g, 6.84 mmol) in portions. The reaction mixture was stirred at 20°C for 2 hours. The resulting mixture was diluted with H20 (15 mL) and extracted with ethyl acetate (15 mL). The aqueous layer was separated and pH was adjusted to 3 by 1 N HC1 and extracted with ethyl acetate (3 x 10 mL). The combined organic layer was washed by brine (10 mL), dried over anhydrous Na2S04 and concentrated under reduced pressure resulting in (i?)-3-(N-sec-butylsulfamoyl)benzoic acid (0.73 g).
To an ice cooled mixture of (i?)-3-(N-sec-butylsulfamoyl)benzoic acid (730 mg), 4-fluoroaniline (347 mg, 3.121mmol), HATU (1.294 g, 3.404 mmol) in DMF (10 mL) DIPEA (1.48 mL, 8.51 mmol) was added under N2 atmosphere. The resulting mixture was stirred at 20°C for 2 hour. The solvent was removed in vacuo. The mixture was washed with saturated aqueous critic acid (10 mL), brine and dried over Na2S04. The solvent was removed in vacuo. The residue was purified by column chromatography over silica gel (gradient eluent: petroleum ether/ethyl acetate from 100/0 to 55/45). The pure fractions were collected and the solvent was removed in vacuo. The residue was purified by SFC separation (Chiralcel OJ, 20 um; Supercritical C02 : MeOH (0.2% diethylamine)). The pure fractions were collected and the solvent was removed in vacuo, resulting in compound 70 (300 mg). Method A; Rt: 5.25 min. m/z : 351.2 (M+H)+ Exact mass: 350.1. [a] = - ( c= 0.2, MeOH). [«]D = -9.9 (c 0.435 w/v %, DMF); Column: Chiralpak AD-3 150x4.6mm I.D., 3um; Mobile phase: methanol
(0.05% diethylamine) in C02 from 5% to 40%; Flow rate: 2.5 mL/min; Rt: 7.58 min; 1H NMR (400 MHz, DMSO-d6) δ ppm 0.70 (t, J=7.4 Hz, 3 H), 0.88 (d, J=6.5 Hz, 3 H), 1.30 (quin, J=7.2 Hz, 2 H), 3.01 - 3.18 (m, 1 H), 7.21 (t, J=8.8 Hz, 2 H), 7.67 (br. d, J=5.5 Hz, 1 H), 7.75 (t, J=7.8 Hz, 1 H), 7.78 (dd, J=8.8, 5.1 Hz, 2 H), 8.00 (d, J=7.8 Hz, 1 H), 8.19 (d, J=7.8 Hz, 1 H), 8.36 (s, 1 H), 10.55 (s, 1 H).
Compound 71
Figure imgf000053_0001
Prepared similar as described for compound 70 starting from (5)-butan-2-amine instead of (i?)-butan-2-amine.Method B; Rt: 4.03 min. m/z : 351.2 (M+H)+ Exact mass: 350.1 ( [«]D = + ( c= 0.2, MeOH).
Figure imgf000053_0002
+ 9.49 (c 0.611 w/v %, DMF), Column: Chiralpak AD-3 150x4.6mm I.D., 3um; Mobile phase: methanol (0.05%> diethylamine) in C02 from 5% to 40%; Flow rate: 2.5 mL/min; Rt: 7.73 min. [ ] 89 +9.49 ° (c 0.61 w/v %, MeOH)
Compound 72
Figure imgf000053_0003
3-(chlorosulfonyl)benzoyl chloride (1200 mg, 5.0 mmol) was dissolved in dichloro- methane (15 mL). A solution of 4-nuoro-3-methylaniline (625 mg, 5.0 mmol) and triethylamine (606 mg, 6.0 mmol) in dichloromethane (15 mL) was added to the mixture at 0°C. The mixture was stirred at 25°C for 1 hour. The reaction mixture was used to the next step without further purification. To the above reaction mixture a solution of triethylamine (606 mg, 6.0 mmol) and (5)-tetrahydrofuran-3 -amine
(460.0 mg, 5.3 mmol) in dichloromethane (15 mL) was added at 0°C. The mixture was stirred at 25 °C for 1 hour. The solvent was removed in vacuo. The residue was purified by reversed phase high performance liquid chromatography (eluent: CH3CN in water (0.1% TFA) from 25 to 55, v/v). The pure fractions were collected and the organic solvent was evaporated. The aqueous layer was neutralized with saturated aqueous NaHCC"3 to pH=7-8. The mixture was extracted with dichloromethane (3 x 15 mL). The combined organic layers were dried over Na2S04 and concentrated in vacuo resulting in compound 72 (620 mg). Method A; Rt: 4.88 min. m/z : 379.2 (M+H)+
Exact mass: 378.1. 1H NMR (400 MHz, DMSO-d6) δ ppm 1.56 - 1.65 (m, 1 H), 1.85 - 1.94 (m, 1 H), 2.22 - 2.28 (m, 3 H), 3.33 - 3.39 (m, 1 H), 3.52 - 3.65 (m, 2 H), 3.65 - 3.73 (m, 1 H), 3.73 - 3.79 (m, 1 H), 7.14 (t, J=9.2 Hz, 1 H), 7.56 - 7.62 (m, 1 H), 7.67 (dd, J=7.0, 2.3 Hz, 1 H), 7.78 (t, J=7.8 Hz, 1 H), 8.02 (d, J=7.8 Hz, 1 H), 8.10 (d, J=4.5 Hz, 1 H), 8.21 (d, J=7.8 Hz, 1 H), 8.37 (s, 1 H), 10.49 (s, 1 H)
Compound 85
Figure imgf000054_0001
Prepared similarly as described for compound 72 using 1-ethylcyclopropanamine hydrochloride instead of (5)-tetrahydrofuran-3-amine. Compound 85 was purified by preparative high performance liquid chromatography over RP-18 (eluent: CH3CN in H20 (0.5% NH4HCO3) from 43% to 73%, v/v). Method B; Rt: 4.17 min. m/z : 377.1 (M+H)+ Exact mass: 376.1. 1H NMR (400 MHz, DMSO-d6) δ ppm 0.35-0.45 (m, 2 H), 0.49-0.58 (m, 2 H), 0.77 (t, J=7.2 Hz, 3 H), 1.31 (q, J=7.1 Hz, 2 H), 2.26 (s, 3 H), 7.15 (t, J=9.3 Hz, 1 H), 7.55 - 7.64 (m, 1 H) 7.69 (d, J=7.0 Hz, 1 H), 7.76 (t, J=7.8 Hz, 1 H), 7.98 (d, J=7.8 Hz, 1 H), 8.16 - 8.25 (m, 2 H), 8.35 (s, 1 H), 10.50 (s, 1 H).
Compound 86
Figure imgf000054_0002
Prepared similarly as described for compound 72 using 2-methylbutan-2-aminehydro- chloride instead of (5)-tetrahydrofuran-3-amine. Purified by high performance liquid chromatography over RP-18 (eluent: CH3CN in water from 47% to 77%, v/v). Method D; Rt: 5.97 min. m/z : 379.1 (M+H)+ Exact mass: 378.1. 1H NMR (400 MHz, DMSO- d6), δ = 0.73 (t, J=7.5 Hz, 3 H), 1.02 (s, 6 H), 1.44 (q, J=7.5 Hz, 2 H), 2.23 (d, J=l .0 Hz, 3 H), 7.12 (t, J=9.3 Hz, 1 H), 7.52 - 7.61 (m, 2 H), 7.64 - 7.77 (m, 2 H), 8.01 (d, J=7.8 Hz, 1 H), 8.14 (d, J=7.8 Hz, 1 H), 8.36 (s, 1 H). 10.45 (s, 1 H).
Alternative synthesis of compound 72:
A mixture of 3-(chlorosulfonyl)benzoyl chloride (4.61 g ,19.28mmol) in toluene
(45 mL) was refluxed under a gentle flow of nitrogen. 4-fluoro-3-methylaniline (2.19 g, 17.53 mmol) in toluene (15 mL) was added drop wise to the refluxing solution. After addition, the mixture was refluxed for another 30 minutes. The mixture was next cooled to room temperature, and a mixture of (S)-3-aminotetrahydrofuran tosylate (5 g, 19.28 mmol) and diisopropylethylamine (15 mL) in toluene (15 mL) and CH2CI2 (10 mL) was added drop wise. After addition, the mixture was stirred for 4 hours at room temperature. The resulting mixture was washed with HC1 (2 x 100 mL, 1M aq), water (2 x 100 mL) and NaHC03 (2 x 100 mL, sat. aq). The organic layer was dried on MgS04, filtered and concentrated under reduced pressure. The obtained residue was purified using silica gel chromatography (CH2Cl2-MeOH 100:0 to 95:5) yielding 3-(4-fluoro-3-methylphenylcarbamoyl)benzene-l-sulfonyl chloride (1.07 g) during CH2CI2 elution, followed by compound 72 (2.85 g) as a white solid after removal of the solvent (dried in a vacuum oven at 55°C for 20 hours). ([OE]D = - 5.21 (c 0.67 w/v %, MeOH), Method F; Rt: 0.88 min. m/z : 379.1 (M+H)+ Exact mass: 378.1. The compound was crystallized from CH2C12: DSC (From 30 to 300 °C at 10°C/min):
149°C. = + 3.21 (c 0.65 w/v %, DMF).
Compound 73
Figure imgf000055_0001
To an iced-cooled solution of 3-(chlorosulfonyl)benzoic acid (50.0 g, 226.6 mmol) in ethylacetate (1000 mL) was added isopropylamine (67.0 g, 1.13 mol) in one portion. The reaction mixture was stirred at 25°C for 3 hours. The resulting mixture was diluted with IN HC1 (500 mL) and extracted with ethyl acetate (2 x 500 mL). The combined organic layers were washed with brine (400 mL), dried over anhydrous Na2S04 and concentrated under reduced pressure resulting 3-(N-isopropylsulfamoyl)benzoic acid (46 g). To an ice-cooled mixture of 3-(N-isopropylsulfamoyl)benzoic acid (7.0 g, 28.77 mmol), 4-fiuoro-3-methylaniline (3.6 g, 28.77 mmol) and DIPEA (18.6 g, 143.91 mmol) in CH2C12 (70 mL) HATU (12.0 g, 31.56 mmol) was added under N2 atmosphere. The resulting mixture was stirred at 20° for 16 hours. The solvent was removed in vacuo. The mixture was washed with saturated aqueous critic acid (30 mL), brine (20 mL) and dried over Na2S04. The solvent was removed in vacuo. The residue was purified by preparative high performance liquid chromatography on SYNERGI 250*50 lOum (eluent: CH3CN in H20 (0.05% TFA) from 35% to 65%, v/v). The pure fractions were collected and adjusted to pH=7 with Amberlite IRA-900(OH) anionic exchange resin. The resin was filtered off. The filtrate was lyophilized to dryness resulting in compound 73 (7.5 g). Method B; Rt: 3.44 min. m/z : 351.1 (M+H)+ Exact mass: 350.1 1H NMR (400 MHz, DMSO-d6) δ ppm 10.49 (1 H, br. s), 8.36 (1 H, t, J=1.5 Hz), 8.19 (1 H, ddd, J=7.8, 1.5, 1.0 Hz), 8.01 (1 H, ddd, J=7.8, 1.5, 1.0 Hz), 7.76 (1 H, t, J=7.8 Hz), 7.68 (1 H, dd, J=7.0, 3.0 Hz), 7.75 (1 H, bs), 7.59 (1 H, ddd, J=9.0, 4.5, 3.0 Hz), 7.15 (1 H, t, J=9.0 Hz), 3.14 - 3.33 (1 H, m), 2.25 (3 H, d, J=1.5 Hz), 0.96 (6 H, d, J=6.5 Hz).
Compound 74
Figure imgf000056_0001
Prepared similarly as described for compound 73, using 4-fluoro-3-(trifluoromethyl)- aniline instead of 4-fluoro-3-methylaniline. Purified on HPLC Synergi 150x30mmx5u (eluent: CH3CN in H20 (0.05% HC1) from 45% to 75%, v/v). Method A; Rt: 5.62 min. m/z : 405.2 (M+H)+ Exact mass: 404.1. 1H NMR (400 MHz, DMSO-d6) δ ppm 10.82 (1 H, s), 8.39 (1 H, t, J=1.5 Hz), 8.17 - 8.30 (2 H, m), 8.07 - 8.17 (1 H, m), 8.03 (1 H, d, J=7.8), 7.73-7.83 (2 H, m), 7.55 (1 H, t, J=10.0 Hz), 3.20 - 3.33 (1 H, m), 0.95 (6 H, d, J=6.5
Figure imgf000056_0002
Compoun
A mixture of N-(3 -bromo-4-fluorophenyl)-3 -(N-isopropylsulfamoyl)benzamide (prepared similarly as described for compound 73, using 3-bromo-4-fluoroaniline instead of 4-fluoro-3-methylaniline and purified via preparative high performance liquid chromatography over RP-18 (eluent: CH3CN in H20 (0.05% NH4HC03) from 40%) to 70%), v/v); 700 mg, 1.69 mmol), cyclopropylboronic acid (0.22 g, 2.529 mmol) Pd(PPh3)4 (0.20 g, 0.169 mmol) and Na2C03 (1.43 g, 13.49 mmol) in water (7 mL), EtOH (7 mL) and toluene (7 mL) was heated by microwave irradiation for 40 minutes at 100°C under N2. The reaction mixture was filtered through celite. Water (10 mL) was added to the filtrate and the mixture was extracted with ethyl acetate (2 x 10 mL). The combined organic layers were washed with brine and dried over Na2S04. The solvent was removed in vacuo. The residue was purified by preparative high
performance liquid chromatography over RP-18 (eluent: CH3CN in H20 (0.1% TFA) from 20%) to 50%>, v/v). The pure fractions were collected and the volatiles were removed in vacuo. The aqueous layer was adjusted to pH=7 with saturated aqueous NaHC03 and extracted with ethyl acetate (2 x 20 mL). The combined organic layers were dried over Na2S04. The solvent was removed in vacuo and the obtained residue was further purified by supercritical fluid chromatography (Column: Chiralpak AD-3 150x4.6mm I.D., 3um Mobile phase: methanol (0.05% diethylamine) in C02 from 5% to 40%. Flow rate: 2.5mL/min). The pure fractions were collected and the volatiles were removed in vacuo. The residue was suspended in water (5 mL) and lyophilized to dryness resulting in compound 84 (35 mg) Method B; Rt: 4.18 min. m/z : 377.1 (M+H)+ Exact mass: 376.1 ; 1H NMR (400 MHz, chloroform-d) δ ppm 8.34 (s, 1 H), 8.12 (d, J=8.0 Hz, 1 H), 7.97 - 8.07 (m, 2 H), 7.65 (t, J=8.0 Hz, 1 H), 7.36 - 7.46 (m, 1 H), 7.15-7.22 (m, 1 H), 7.01 (t, J=9.3 Hz, 1 H), 4.65 (d, J=7.5 Hz, 1 H), 3.44-3.58 (m, 1 H), 2.04 - 2.16 (m, 1 H), 1.10 (d, J=6.5 Hz, 6 H), 0.96 - 1.06 (m, 2 H), 0.71 - 0.82 (m, 2 H).
Compound 88
Figure imgf000057_0001
Prepared similarly as described for compound 73, using 3,4-difluoroaniline instead of 4-fluoro-3-methylaniline. Method E; Rt: 5.31 min. m/z : 355.1 (M+H)+ Exact mass: 354.1 ; 1H NMR (400 MHz, DMSC /6) δ ppm 10.71 (s, 1 H), 8.36 (t, J=1.5 Hz, 1 H), 8.19 (d, J=7.8 Hz, 1 H), 7.98 - 8.08 (m, 1 H), 7.94 (ddd, J=13.2, 7.5, 2.4 Hz, 1 H), 7.71 - 7.83 (m, 2 H), 7.53 - 7.59 (m, 1 H), 7.42 - 7.51 (m, 1 H), 3.21 - 3.29 (m, 1 H), 0.96 (d, J=6.5 Hz, 6
Compound
Figure imgf000057_0002
3-(chlorosulfonyl)benzoyl chloride (1200 mg, 5.0 mmol) was dissolved in dichloro- methane (15 mL). A solution of 3,4-difluoroaniline (650 mg, 5.0 mmol) and triethylamine (606 mg, 6.0mmol) in dichloromethane (15 mL) was added to the mixture at 0°C. The mixture was stirred at 25°C for 1 hour. To the obtained reaction mixture a solution of triethylamine (606 mg, 6.0 mmol) and (S)-tetrahydrofuran- 3-amine (460.0 mg, 5.3mmol) in dichloromethane (15 mL) was added at 0°C. The mixture was stirred at 25°C for 1 hour. The solvent was removed in vacuo. The obtained residue was purified by high performance liquid chromatography over RP-18 (eluent: CH3CN in water (0.1%TFA) from 30 to 60, v/v). The pure fractions were collected and the organic solvent was evaporated. The aqueous layer was neutralized with saturated aqueous NaHC03 to pH=7-8. The mixture was extracted with dichloromethane (3 x 15 mL). The combined organic layers were dried over Na2S04 and concentrated in vacuo resulting in compound 90 (710 mg) Method A; Rt: 4.16 min. m/z : 383.0 (M+H)+ Exact mass: 382.1; 1H NMR (400 MHz, DMSO-d6) δ ppm 1.54 - 1.63 (m, 1 H), 1.83 - 1.93 (m, 1 H), 3.32 - 3.38 (m, 1 H), 3.52 - 3.63 (m, 2 H), 3.63 - 3.77 (m, 2 H), 7.45 (dt, J=10.5, 9.0 Hz, 1 H), 7.51 - 7.57 (m, 1 H), 7.78 (t, J=7.8 Hz, 1 H), 7.92 (ddd, J=13.3, 7.5, 2.5 Hz, 1 H), 8.02 (d, J=7.8Hz, 1 H), 8.09 (d, J=6.5 Hz, 1 H), 8.20 (d, J=7.8 Hz, 1 H), 8.35 (s, 1 H), 10.70 (s, 1 H). SFC: Column: Chiralcel OJ-H 250x4.6mm I.D., 5um; Flow: 2.35 mL/min; Mobile phase: methanol (0.05%
diethylamine) in C02 from 5% to 40%; Rt: 5.61 Μίη.[ ]η = + 3.21 (c 0.624 w/v %, DMF)
Compound 91
Figure imgf000058_0001
N-(3-bromo-4-fluorophenyl)-3-(N-isopropylsulfamoyl)benzamide (1.5 g, 3.61 mmol), ethynyltrimethylsilane (1.77 g, 18.06 mmol), Pd(PPh3)2Cl2 (0.127g, 0.181mmol) and copper iodide (34.4 mg, 0.181mmol) were dissolved in diisopropylamine (10 mL). The mixture was stirred at 80°C in autoclave for 24 hours. The solvent was removed in vacuo and dichloromethane (30 mL) was added. The mixture was washed with water (20 mL) and the aqueous layer was extracted with dichloromethane (20 mL). The combined organic layers were washed with brine and dried over Na2S04. The solvent was removed in vacuo. The obtained residue was purified by silica gel column chromatography (eluent: petroleum ether / ethyl acetate from 100/1 to 60/40) resulting in N-(4-fluoro-3-((trimethylsilyl)ethynyl)phenyl)-3-(N-isopropylsulfamoyl)benzamide (0.8 g) . N-(4-fluoro-3 -((trimethylsilyl)ethynyl)phenyl)-3 -(N-isopropylsulfamoyl)- benzamide (0.8 g, 1.66 mmol) and TFA (4 mL) were dissolved in anhydrous CH2CI2 (16 mL). The mixture was stirred at 25°C overnight and next concentrated in vacuo. The obtained residue was purified by silica gel column chromatography (gradient eluent: petroleum ether/ethyl acetate from 100/0 to 75/25) resulting in compound 91 (220 mg). Method A; Rt: 5.12 min. m/z : 361.3 (M+H)+ Exact mass: 360.1. 1H NMR (400 MHz, DMSO-dg) δ ppm 10.60 (1 H, s), 8.35 (1 H, t, J=1.5 Hz), 8.18 (1 H, d, J=8.0 Hz), 8.00 (1 H, d, J=8.0 Hz), 7.97 (1 H, dd, J=6.5, 3.0 Hz), 7.77 - 7.84 (1 H, m), 7.70 - 7.79 (2 H, m), 7.32 (1 H, t, J=9.0 Hz), 4.52 (1H, s) 3.22 - 3.31 (1 H, m), 0.94 (6 H, d, J=6.5 Hz).
Compound 92
Figure imgf000059_0001
N-(4-fluoro-3-((trimethylsilyl)ethynyl)phenyl)-3-(N-isopropylsulfamoyl)benzamide (0.8g, 1.66mmol) and TFA (4 mL) were dissolved in anhydrous CH2CI2 (16 mL). The mixture was stirred at 25° overnight. The mixture was concentrated resulting in crude N-(3-ethynyl-4-fluorophenyl)-3-(N-isopropylsulfamoyl)benzamide which was used as such in the next step (650 mg). To a solution of N-(3-ethynyl-4-fluorophenyl)-3- (N-isopropylsulfamoyl)benzamide (0.6 g) in MeOH (20 mL) was added Pd-C (10%, 0.2 g) under N2 atmosphere. The mixture was stirred under hydrogen atmosphere (50 psi) at 25°C for 4 hours. After filtration on celite, the solvent was removed in vacuo and the obtained residue was purified by preparative high performance liquid chromatography on reversed phase C-18 (eluent: CH3CN in H20 (0.05%> HC1) from 42%) to 72%), v/v). The pure fractions were collected and the volatiles were removed in vacuo. The aqueous layer was adjusted to PH=7 with Amberlite IRA-900 anionic exchange resin (OH form), filtered and lyophilized to dryness resulting in compound 92 (160 mg). Method B; Rt: 4.13 min. m/z : 365.3 (M+H)+ Exact mass: 364.1; 1H NMR (400 MHz, DMSO-dg) δ ppm 10.48 (1 H, s), 8.35 (1 H, t, J=1.5 Hz), 8.18 (1 H, d, J=8.0 Hz), 7.99 (1 H, d, J=8.0 Hz), 7.70 - 7.78 (2 H, m), 7.65 - 7.70 (1 H, m), 7.57 - 7.65 (1 H, m), 7.13 (1 H, t, J=9.0 Hz), 3.21 - 3.32 (1 H, m), 2.62 (2 H, q, J=7.5 Hz), 1.18 (3 H, t, J=7.5 Hz), 0.94 (6 H, d, J=6.5 Hz). Compound 93
Figure imgf000060_0001
To a solution of 3-(chlorosulfonyl)benzoyl chloride (0.50 g, 2.09 mmol) in CH2CI2 (10 mL), DIPEA was added (1.35 g, 10.45 mmol) followed by slow addition of 4-fluoro-3-methylaniline (0.25 g, 1.99 mmol). After stirring at 25°C for 0.5 hour, 3-ethyloxetan-3-amine (0.21 g, 2.09 mmol) was added. After 1 hour, the resulting mixture was diluted with CH2CI2 (15 mL), washed with saturated aqueous NaHC03 (15 mL) and brine (10 mL) and dried over anhydrous MgSC^. The solvent was removed in vacuo and the obtained residue was purified by silica gel column chromatography (gradient eluent: petroleum ether/ethyl acetate from 100/0 to 80/20) resulting in compound 93 (70 mg). Method B; Rt: 3.79 min. m/z : 393.3 (M+H)+ Exact mass: 392.1; 1H NMR (400 MHz, DMSO-d6) δ ppm 10.50 (1 H, s), 8.47 (1 H, br. s), 8.38 (1 H, t, J=1.5 Hz), 8.22 (1 H, d, J=8.0 Hz), 8.03 (1 H, d, J=8.0 Hz), 7.78 (1 H, t, J=8.0 Hz), 7.68 (1 H, dd, J=7.5, 2.5 Hz), 7.56 - 7.64 (1 H, m), 7.15 (1 H, t, J=9.0 Hz), 4.51 (2 H, d, J=6.5 Hz), 4.19 (2 H, d, J=6.5 Hz), 2.25 (3 H, d, J=1.5 Hz), 1.84 (2 H, q, J=7.0 Hz), 0.64 (3 H, t, J=7.0 Hz).
Compound 94
Figure imgf000060_0002
3-(chlorosulfonyl)benzoyl chloride (1200 mg, 5.0 mmol) was dissolved in dichloro- methane (15 mL). A solution of 4-fluoro-3-methylaniline (625 mg, 5.0 mmol) and triethylamine (606 mg, 6.0 mmol) in dichloromethane (15 mL) was added to the mixture at 0°C. The mixture was stirred at 25°C for 1 hour. The reaction mixture was used to the next step without further purification (crude, 30 mL). To the above reaction mixture was added a solution of triethylamine (606 mg, 6.0 mmol) and 1-methylcyclo- propanamine (425.0 mg, 5.9 mmol) in dichloromethane (15 mL) at 0°C. The mixture was stirred at 25°C for 1 hour. The solvent was removed in vacuo. The residue was purified by high performance liquid chromatography on reversed phase (eluent:
CH3CN in water from 40% to 70%, v/v). The pure fractions were collected and the organic solvent was evaporated. The aqueous layer was neutralized with saturated aqueous NaHC03 to pH=7-8. The mixture was extracted with dichloromethane (3 x 15 mL). The combined organic layers were dried over Na2S04 and concentrated in vacuo resulting in compound 94 (365 mg). Method B; Rt: 3.40 min. m/z : 363.0 (M+H)+ Exact mass: 362.1; 1H NMR (400 MHz, DMSO-d6) δ ppm 10.49 (1 H, s), 8.35 (1 H, t, J=1.5 Hz), 8.17 - 8.23 (2 H, m), 7.99 (1 H, d, J=8.0 Hz), 7.76 (1 H, t, J=8.0 Hz), 7.68 (1 H, dd, J=7.0, 2.5 Hz), 7.56 - 7.62 (1 H, m), 7.14 (1 H, t, J=9.0 Hz), 2.25 (3 H, d, J=l .5 Hz), 1.06 (3 H, s), 0.58 - 0.63 (2 H, m), 0.37 - 0.42 (2 H, m)
Compound 95
Figure imgf000061_0001
A mixture of N-(3-bromo-4-fluorophenyl)-3-(N-isopropylsulfamoyl)benzamide (800 mg, 1.93 mmol), 4,4,5,5-tetramethyl-2-(prop-l-en-2-yl)-l,3,2-dioxaborolane (0.65 g, 3.85 mmol), Pd(PPh3)4 (111 mg, 0.096 mmol)) and K2C03 (0.53 g, 3.85 mmol) in dioxane (8 mL) and water (2 mL) was heated by microwave irradiation for 110 minutes at 120°C under N2 atmosphere. The reaction mixture was diluted with ethyl acetate (20 mL) and the catalyst was filtered off. The filtrate was concentrated in vacuo. Water (20 mL) was added and the aqueous layer was extracted with ethyl acetate (2 x 20 mL). The combined organic layers were washed with brine and dried over Na2S04. The solvent was removed in vacuo and the obtained residue was purified by preparative high performance liquid chromatography over reversed phase C-18 (eluent: CH3CN in H20 (0.1 % TFA) from 40% to 70%, v/v). The pure fractions were collected and the organic solvent was removed in vacuo. The aqueous layer was lyophilized to dryness resulting in N-(4-fluoro-3-(prop-l-en-2-yl)phenyl)-3-(N-iso- propylsulfamoyl)benzamide (300 mg). N-(4-fluoro-3-(prop-l-en-2-yl)phenyl)-3- (N-isopropylsulfamoyl)benzamide (180 mg) and Pd/C(wet) (20 mg) were stirred in methanol (4 mL) under a hydrogen atmosphere at 25°C for 3 hours. The mixture was filtered over celite and the filtrate was evaporated to dryness in vacuo. The residue was purified by silica gel column chromatography (gradient eluent: petroleum ether/ethyl acetate from 100/0 to 70/30). The volatiles were removed in vacuo, resulting in compound 95 (175 mg). Method B; Rt: 4.33 min. m/z : 379.3 (M+H)+ Exact mass: 378.1; Compound 96
Figure imgf000062_0001
3-(difluoromethyl)-4-fluoroaniline (1.20 g, 7.448 mmol), 3-(N-isopropylsulfamoyl)- benzoic acid (0.90 g, 3.699 mmol) and DIPEA (1.93 mL, 11.10 mmol) were dissolved in CH2C12 (10 mL) and HATU (1.41 g, 3.699 mmol) was added at 0°C. The mixture was stirred at 20 °C for 2 hours. The mixture was diluted with CH2CI2 (10 mL) and H20 (10 mL). The organic layer was separated, washed with saturated aqueous NaHC03 (10 mL) and brine (10 mL) and dried over Na2S04. The solvent was removed in vacuo and the obtained residue was purified by preparative high performance liquid chromatography over reversed phase C- 18 (eluent: CH3CN in H20 (0.1 %o NH4HCO3) from 45% to 75%>, v/v). The pure fractions were collected and the organic solvent was removed in vacuo. The aqueous layer was lyophilized to dryness resulting in compound 96 (0.885 g). Method A; Rt: 5.16 min. m/z : 387.3 (M+H)+ Exact mass: 386.1; 1H NMR (400 MHz, DMSO-d6) δ ppm 10.72 (1 H, s), 8.38 (1 H, t, J= 1.5 Hz), 8.21 (1 H, d, J= 8.0 Hz), 8.06 - 8.13 (1 H, m), 8.02 (1 H, d, J= 8.0 Hz), 7.92 - 8.00 (1 H, m), 7.72 - 7.82 (2 H, m), 7.40 (1 H, t, J= 9.5 Hz), 7.25 (1 H, t, J= 55 Hz), 3.23 - 3.32 (1 H, m), 0.95 (6 H, d, J= 6.5 Hz).
Compound 97
Figure imgf000062_0002
To 3-(4-fluoro-3-methylphenylcarbamoyl)benzene-l-sulfonyl chloride (500 mg, 1.53 mmol) in toluene (10 mL) at room temperature, a solution of diisopropyl- ethylamine (0.657 mL, 141.6 mmol) and 3-methyl-3-oxetanamine hydrochloride (207 mg, 1.68 mmol) in toluene (5 mL) and dichloromethane (10 mL) was added drop wise. After 2 hours, the reaction mixture was washed with 1M hydrochloric acid (2 x 10 mL, saturated NaHC03 (2 x 10 mL) and brine (2 x 10 mL). The organic layer was dried on MgS04, filtered and concentrated under reduced pressure until only toluene remained. The formed white precipitate was filtered and recrystallised out of diisopropylether and acetonitrile. The crystals were dried in a vacuum oven at 55 °C for 20 hours yielding compound 97 (361 mg) as a white solid. Method F; Rt: 0.89 min. m/z : 379.0 (M+H)+ Exact mass: 378.1; 1H NMR (400 MHz, DMSO-d6) δ ppm 1.41 (s, 3 H), 2.25 (d, J=1.5 Hz, 3 H), 4.14 (d, J=6.3 Hz, 2 H), 4.56 (d, J=6.3 Hz, 2 H), 7.14 (t, J=9.0 Hz, 1 H), 7.52 - 7.64 (m, 1 H), 7.68 (dd, J=7.0, 2.2 Hz, 1 H), 7.77 (t, J=8.0 Hz, 1 H), 7.99 - 8.06 (m, 1 H), 8.20 (d, J=8.0 Hz, 1 H), 8.37 (t, J=1.5 Hz, 1 H), 8.50 (br. s., 1 H), 10.48 (s, 1 H).
Compound 98
Figure imgf000063_0001
To 3-(4-fluoro-3-methylphenylcarbamoyl)benzene-l-sulfonyl chloride (500 mg, 1.53 mmol) in toluene (10 mL) at room temperature, a solution of diisopropylethyl- amine (0.657 mL, 141.6 mmol) and (i?)-(-)-2-aminobutane (130 mg, 1.83 mmol) in toluene (5 mL) and dichloromethane (10 mL) was added drop wise. After 2 hours, the reaction mixture was washed with 1M aqueous HC1 (2 x10 mL), NaHC03 (2 x 10 mL) and brine (2 x 10 mL). The organic layer was dried on MgS04, filtered and
concentrated under reduced pressure until only toluene remained. The formed white precipitate was filtered, recrystallised (diisopropylether and acetonitrile) and dried in vacuo at 55°C for 20 hours resulting in compound 98 (257 mg) as a white solid.
Method F; Rt: 1.04 min. m/z : 382.1 (M+NH4)+ Exact mass: 364.1; 1H NMR
(400 MHz, DMSO-dg) δ ppm 0.71 (t, J=7.5 Hz, 3 H), 0.88 (d, J=6.6 Hz, 3 H), 1.31 (quin, J=7.5 Hz, 2 H), 2.25 (d, J=1.8 Hz, 3 H), 3.05-3.18 (m, 1 H), 7.14 (t, J=9.0 Hz, 1 H), 7.55 - 7.62 (m, 1 H), 7.63 - 7.72 (m, 2 H), 7.75 (t, J=8.0 Hz, 1 H), 8.00 (d, J=8.0 Hz, 1 H), 8.18 (d, J=8.0 Hz, 1 H), 8.36 (t, J=1.5 Hz, 1 H), 10.46 (s, 1 H).
Compound 99
Figure imgf000063_0002
A mixture of 3-(N-isopropylsulfamoyl)benzoic acid (2.3 g, 9.615 mmol), 3-bromo-4,5- difluoroaniline (2 g, 9.615 mmol) and DIPEA (5 mL) in CH2CI2 (30 mL) was cooled to 0°C and HATU (4.39 g, 1 1.538 mmol) was added. The mixture was stirred for 2 hours at 20°C. The mixture was washed with IN HC1 (30 mL) and brine (30 mL) and dried over Na2S04. The solvent was removed in vacuo. The residue was purified by silica gel column chromatography (gradient eluent: petroleum ether/ethyl acetate from 100/0 to 70/30) resulting in crude N-(3-bromo-4,5-difluorophenyl)-3-(N-isopropylsulfamoyl)- benzamide (4 g). A mixture of N-(3-bromo-4,5-difluorophenyl)-3-(N-isopropyl- sulfamoyl)benzamide (1 g, 2.308 mmol), methylboronic acid (1 g, 4.616 mmol), CS2CO3 (2.26 g, 6.924 mmol), 2-Dicyclohexylphosphino-2',6'-dimethoxybiphenyl (95 mg, 0.231 mmol) and Tris(dibenzylideneacetone)dipalladium(0) (0.21 g,
0.231 mmol) in dioxane (15 mL) was heated by microwave irradiation for 40 minutes at 120°C under N2 atmosphere. After cooling, the mixture was filtered through celite and the filtrate was evaporated to dryness. The obtained residue was purified by silca gel column chromatography (gradient eluent: petroleum ether/ethyl acetate from 100/0 to 70/30) and further purified by preparative high performance liquid chromatography over reversed phase C-18 (eluent: CH3CN in H20 (0.1% TFA) from 38% to 68%, v/v). The pure fractions were collected and half of the volatiles were removed in vacuo. The mixture was adjusted to pH=7 with Amberlite IRA-900 (OH) anionic exchange resin and the resin was filtered off. The organic solvent was concentrated in vacuo and the aqueous layer was lyophilized to dryness. The obtained product was further purified by silica gel chromatography (gradient eluent: petroleum ether/ethyl acetate from 100/0 to 70/30) resulting in compound 99 (190 mg). Method A; Rt: 6.09 min. m/z : 369.2 (M+H)+ Exact mass: 368.1, 1H NMR (400 MHz, CHLOROFORM- ) δ ppm 8.35 (1 H, t, J=1.5 Hz), 8.09 - 8.17 (2 H, m), 8.04 (1 H, dt, J=8.0, 1.5 Hz), 7.66 (1 H, t, J=8.0 Hz), 7.54 (1 H, ddd, J=11.5, 6.5, 3.0 Hz), 7.14 - 7.22 (1 H, m), 4.72 (1 H, d, J=8.0 Hz), 3.43-3.60 (1 H, m), 2.32 (3 H, d, J=2.0 Hz), 1.10 (6 H, d, J=6.5 Hz).
Compound 100
Figure imgf000064_0001
5-(chlorosulfonyl)-2-fluorobenzoic acid (7g, 29.3 mmol) was dissolved in dichloro- methane (70 mL). DMF (0.7 mL) was added, followed by drop wise addition of oxalyl chloride (4.46 g, 35.16 mmol) at 0°C. The mixture was stirred for 1 hour at 20°C. The mixture was concentrated in vacuo and the crude 5-(chlorosulfonyl)-2-fluorobenzoyl chloride was dissolved in dichloro methane (15 mL). A solution of 3,4-difluoroaniline (3.6g, 27.87 mmol ) and DIPEA (4.6g, 35.20 mmol) in dichloromethane (60 mL) was added to the mixture at 0°C. The mixture was stirred at 25°C for 1 hour and used to the next step directly. To the above reaction mixture, a solution of (i?)-(-)-2-aminobutane (2.2 g, 29.34 mmol) and DIPEA (4.6g, 35.20 mmol) in dichloromethane (60 mL) was added at 0°C. The resulting mixture was stirred at 25°C for 1 hour. The mixture was concentrated in vacuo and the obtained residue was purified by high performance liquid chromatography on reversed phase (eluent: CH3CN in water (0.1% TFA) from 25% to 55%, v/v). The pure fractions were collected and the organic solvent was evaporated. The aqueous solution was adjusted to pH =7 with saturated aqueous NaHC03. The mixture was extracted with dichloromethane (3 x 200 mL). The combined organic layers were dried over Na2S04 and concentrated in vacuo. The obtained residue was suspended in water (10 mL) and the aqueous layer was lyophilized to dryness resulting in compound 100 (4.7 g). Method B; Rt: 4.70 min. m/z : 387.2 (M+H)+ Exact mass: 386.1.
Compound 101
Figure imgf000065_0001
(S)-tetrahydrofuran-3 -amine hydrochloride (5.17 g, 42 mmol) and NaOH (5 g, 126 mmol) were dissolved in THF (50 mL) and H20 (50 mL). 5-(chlorosulfonyl)-2- fluorobenzoic acid (10 g, 42 mmol) was added at 0°C. The mixture was stirred at 20°C for 4 hours. The mixture was washed with ethyl acetate (3 x 20 mL). The aqueous layer was separated and adjusted to pH=3 with IN HC1. The aqueous layer was extracted with ethyl acetate (3 x 50 mL). The combined organic layers were washed with brine and dried over Na2S04. The solvent was removed in vacuo resulting in (S)-2-fluoro-5- (N-(tetrahydrofuran-3-yl)sulfamoyl)benzoic acid (2.1 g) . (S)-2-fluoro-5-(N-(tetra- hydrofuran-3-yl)sulfamoyl)benzoic acid (1 g, 3.457 mmol), 3,4-difluoroaniline (0.53 g, 4.15 mmol) and triethylamine (0.7 g, 6.9 mmol) were dissolved in DMF (400 mL) and HATU (1.57 g , 4.15 mmol) was added at 0°C. The mixture was next stirred at 20°C for 6 hours. The solvent was removed in vacuo and the obtained residue was purified by silica gel chromatography (eluent: petroleum ether: ethyl acetate=5 : l) resulting in compound 101 (0.8 g). Method B; Rt: 4.15 min. m/z : 401.3 (M+H)+ Exact mass: 400.1 Synthesis of 3-[[(35)-tetrahydrofuran-3-yl]sulfamoyl]benzoic acid:
(35)-tetrahydrofuran-3 -amine hydrochloride (5.6 g, 45.3 mmol) and NaOH (5.2 g, 130 mmol) were dissolved in THF (50 mL) and H20 (50 mL). 3-(chlorosulfonyl)- benzoic acid (10 g, 45.325 mmol) was added at 0°C. The mixture was stirred at 20°C for 4 hours. The aqueous layer was separated and the pH was adjusted to 2 with IN HC1. The mixture was washed with ethyl acetate (3 x 100 mL).The combined organic layers were concentrated in vacuo resulting in 3-[[(35)-tetrahydrofuran-3- yl]sulfamoyi]benzoic acid (1 1.2 g). Compound 102
Figure imgf000066_0001
A mixture of (5)-tetrahydrofuran-3-amine hydrochloride (11.2 g, 90.7 mmol) and NEt3 (50.5 mL, 362.6 mmol) in dry CH2CI2 (400 mL) was stirred for 5 minutes at 20° C. 3-(chlorosulfonyl)benzoic acid (20 g, 90.7 mmol) was added and the mixture was stirred overnight at 20°C. The reaction mixture was washed with IN HCl (100 mL), the aqueous layer was extracted with dichloromethane (2 x 200 mL). The combined organic layers were dried over Na2S04 and the solvent was removed in vacuo, resulting in 3-[[(35)-tetrahydrofuran-3-yl]sulfamoyl]benzoic acid (16.3 g). 3-[[(35)-tetrahydro- furan-3-yl]sulfamoyl]benzoic acid (3 g, 11.058 mmol), 3-(difluoromethyl)-4-fluoro- aniline (2.1 g, 13.3 mmol) and triethylamine (3.3 g, 33 mmol) were dissolved in DMF (400 mL). PyBrOP (132705-51-2, 6.2 g , 13.3 mmol) was added at 0°C. The mixture was stirred at 50°C for 12 hours. The solvent was removed in vacuo and the obtained residue was purified by reversed phase high performance liquid chromatography (mobile phase: CH3CN in water (0.1% TFA) from 30% to 60%). The pure fractions were collected and neutralized with solid NaHC03. The organic solvent was removed in vacuo and the formed precipitate was filtered, washed with H20 (5 mL) and dried under high vacuum. The obtained residue was suspended in water (5 mL) and lyophilized to dryness resulting in compound 102 (2.3 g). Method A; Rt: 5.32 min. m/z : 415.2 (M+H)+ Exact mass: 414.1. 1H NMR (400 MHz, DMSO-d6) δ ppm 1.53 - 1.68 (m, 1 H) 1.82 - 1.99 (m, 1 H) 3.27 - 3.42 (m, 1 H) 3.51 - 3.90 (m, 4 H) 7.26 (t, J=55 Hz, 1 H) 7.36 - 7.51 (m, 1 H) 7.80 (t, J=7.8 Hz, 1 H) 7.92 - 8.00 (m, 1 H) 8.01 - 8.08 (m, 1 H) 8.08 - 8.15 (m, 2 H) 8.25 (d, J=7.8 Hz, 1 H) 8.40 (s, 1 H) 10.75 (s, 1 H).
Compound 103
Figure imgf000066_0002
3-[[(35)-tetrahydrofuran-3-yl]sulfamoyl]benzoic acid (400 mg, 1.47 mmol) was dissolved in DMF (0.5 mL) and CH2C12 (10 mL). (COCl)2 (223 mg, 1.76 mmol) was added at 0°C. The mixture was stirred at 20°C for 2 hours. The solvent was removed in vacuo and the obtained residue was co-evaporated with toluene (2 x 10 mL) resulting in crude 3-[[(3S)-tetrahydrofuran-3-yl]sulfamoyl]benzoyl chloride (400 mg).The crude product was used in the next step without purification. 3-[[(3S)-tetrahydrofuran-3-yl]- sulfamoyl]benzoyl chloride (200 mg) was dissolved in dichloromethane (5 mL).
4-fluoro-3-methoxy-aniline (78 mg, 0.552 mmol) and triethylamine (167 mg, 165 mmol) were added at 0°C. The mixture was stirred at 20°C for 2 hours, washed with H20 (5 mL) and the waterlayer extracted with dichloromethane (3 x 10 mL). The combined organic layers were concentrated in vacuo. The obtained residue was purified by reversed phase high performance liquid chromatography (mobile phase: CH3CN in water (0.1% TFA) from 30% to 60%). The pure fractions were collected and neutralized with solid NaHC03. The organic solvent was removed in vacuo. The obtained precipitate was filtered, washed with H20 (5 mL) and dried under high vacuum. The residue was suspended in water (5 mL) lyophilized to dryness resulting in compound 103 (140 mg). Method A; Rt: 4.98 min. m/z : 395.2 (M+H)+ Exact mass: 394.1
Prepared similarly as described for compound 103:
Compound 104
Figure imgf000067_0001
Method A; Rt: 5.17 min. m/z: 397.3 (M+H) Exact mass: 396.1
Compound 105
Figure imgf000067_0002
Method A; Rt: 5.10 min. m/z: 389.1 (M+H) Exact mass: 390
Compound 106
Figure imgf000067_0003
Method A; Rt: 5.18 min. m/z : 397.2 (M+H) Exact mass: 396.1
1H NMR (400 MHz, DMSO-d6) δ ppm 1.54 - 1.69 (m, 1 H) 1.82 - 1.98 (m, 1 H) 2.24 (s, 3 H) 3.35 - 3.40 (m, 1 H) 3.52 - 3.66 (m, 2 H) 3.66 - 3.83 (m, 2 H) 7.32 (t, J=10.0 Hz, 1 H) 7.49 (t, J=8.5 Hz, 1 H) 7.79 (t, J=7.8 Hz, 1 H) 8.04 (d, J=8.0 Hz, 1 H) 8.07 - 8.18 (m, 1 H) 8.23 (d, J=7.8 Hz, 1 H) 8.39 (s, 1 H) 10.40 (br. s, 1 H) Compound 107
Figure imgf000068_0001
3-[[(3S)-tetrahydrofuran-3-yl]sulfamoyl]benzoic acid (270 mg, 1.0 mmol) was dissolved in dichloromethane (5 mL). 3-methyl-4-methoxyaniline (165 mg, 1.2 mmol) and triethylamine (145 mg, 1.4 mmol) were added to the mixture at 20°C. The mixture was stirred at 20°C for 5 minutes. HATU (456 mg, 1.2 mol) was added and the mixture was further stirred at 20°C for 8 hours. The solvent was removed in vacuo and the obtained residue was purified by high performance liquid chromatography (Column: Phenomenex Synergi C18 150*20mm*5um.. A: H2O+0.1%TFA B: MeCN from 30% to 60 % B in A). The product fractions were collected and the organic solvent was evaporated in vacuo. The aqueous layer was neutralized with saturated aqueous
NaHCC>3 and extracted with dichloromethane (2 x 10 mL). The combine organic layers was dried over Na2S04 and concentrated in vacuo resulting in compound 107 (135 mg). Method A; Rt: 5.24 min. m/z : 391.3 (M+H)+ Exact mass: 390.1
Compound 108
Figure imgf000068_0002
5-amino-2-fluoro-phenol (234 mg, 1.84 mmol) and 3-[(3-methyloxetan-3-yl)- sulfamoyl]benzoic acid (500 mg, 1.84 mmol) were dissolved in dichloromethane (8 mL). PyBrOP (132705-51-2, 1030 mg, 2.21 mmol) was added followed by drop wise addition of DIPEA (714 mg, 5.53 mmol) at 0°C. The mixture was stirred for 1 hour at 25°C. The mixture was washed with saturated aqueous citric acid (15 mL), saturated aqueous NaHCC (15 mL) and brine and dried over Na2S04. The solvent was removed in vacuo. The obtained residue was purified by reversed phase preparative high-performance liquid chromatography (mobile phase: CH3CN in water (0.05% NH4HCO3) from 29% to 39%>). The pure fractions were collected and the volatiles were removed in vacuo. The residual aqueous layer was lyophilized to dryness re suiting in compound 108 (60 mg). Method A; Rt: 4.47 min. m/z: 381.2 (M+H)+ Exact mass: 380.1
Compound 109
Figure imgf000068_0003
Prepared similarly as described for compound 108, using 4-fluoro-3-methoxy-aniline instead of 5-amino-2-fluoro-phenol. Method A; Rt: 5.03 min. m/z: 395.2 (M+H)+ Exact mass: 394.1
Compound 110
Figure imgf000069_0001
DIPEA (2.85 g, 22.08 mmol) was added to a solution of 3-[(3-methyloxetan-3-yl)- sulfamoyl]benzoic acid (3.0 g, 11.06 mmol) and HATU (4.20 g, 11.05 mmol) in DMF (100 mL) at 25°C. After 30 minutes, 3-bromo-4-fluoro-aniline (2.1 g, 11.05 mmol) was added to the solution. The reaction mixture was stirred at 25°C overnight. The solvent was removed in vacuo and the obtained residue was purified by silica gel column chromatography (gradient eluent: petroleum ether/ethyl acetate from 10/1 to 5/1). The pure fractions were collected and the solvent was removed in vacuo resulting in N-(3- bromo-4-fluoro-phenyl)-3-[(3-methyloxetan-3-yl)sulfamoyl]benzamide (compound 160, 2.5 g). A mixture of N-(3-bromo-4-fluoro-phenyl)-3-[(3-methyloxetan-3- yl)sulfamoyl]benzamide (0.3 g, 0.68 mmol), 4,4,5,5-tetramethyl-2-vinyl-l,3,2- dioxaborolane (54.2 mg, 0.35 mmol), Pd (dppf) Cl2 (50 mg, 0.068 mmol), KOAc (108 mg, 1.1 mmol) and Na2C03 (100 mg, 0.94 mmol) in CH3CN (10 mL) and H20 (2 mL) was heated by microwave irradiation for 30 minutes at 130°C under a N2 atmosphere. The reaction mixture was filtered through Celite and the filter cake was washed with ethyl acetate (2 x 10 mL). The organic layer was separated from the filtrate, washed with brine and dried over Na2S04. The solvent was removed in vacuo. The obtained residue was purified by reversed phase preparative high performance liquid
chromatography (eluent: CH3CN in H20 (0.05% NH3.H20) from 30% to 80%, v/v). The pure fractions were collected and the volatiles were removed in vacuo. The aqueous layer was lyophilized to dryness resulting in compound 110 (70 mg). Method B; Rt: 4.19 min. m/z : 391.3 (M+H)+ Exact mass: 390.1.
Compound 111
Figure imgf000069_0002
3-[(3-methyloxetan-3-yl)sulfamoyl]benzoic acid (3 g, 11.06 mmol), methyl 5-amino-2- fluoro-benzoate (2.33 g, 13.2 mmol) and DIPEA (2.84 g, 22 mmol) were dissolved in DMF (40 mL). HATU (5.02 g , 13.2 mmol) was added at 0°C. The mixture was stirred at 20°C for 2 hours. The solvent was removed in vacuo and the obtained residue was purified by silica gel column chromatography (eluent: petroleum ether: ethyl acetate=3: l) resulting in methyl 2-fluoro-5-[[3-[(3-methyloxetan-3-yl)sulfamoyl]- benzoyl]amino]benzoate (2.3 g). Methyl 2-fluoro-5-[[3-[(3-methyloxetan-3-yl)- sulfamoyl]benzoyl]amino]benzoate (0.3 g, 0.71 mmol) was dissolved in THF (5 mL) and ethanol (5 mL). NaBH4 (53 mg, 1.4 mmol) was added at 0°C. The mixture was stirred for 2 hours at 20°C. The solvent was removed in vacuo and the obtained residue was purified by reversed phase high performance liquid chromatography (mobile phase: CH3CN in water (0.1 % TFA) from 34% to 64%). The pure fractions were collected and neutralized with solid NaHC03. The organic solvent was removed in vacuo. The precipitate was filtered, washed with H20 (5 mL) and dried under high vacuum. The residue was suspended in water (5 mL) and the aqueous layer was lyophilized to dryness resulting in compound 111 (220 mg). Method A; Rt: 4.34 min. m/z : 395.3 (M+H) Exact mass: 394
Compound 127
Figure imgf000070_0001
(2-fluoro-5-nitro-phenyl)methanol (4.3 g, 25.1 mmol) was dissolved in dichloro- methane (50 mL). Diethylaminosulfur trifluoride (4.5 g, 27.9 mmol) was added drop wise to the mixture at -30°C. The mixture was stirred at 10° C for 4 hours. Methanol (10 mL) was added to the mixture and the mixture was further stirred at 10°C for 30 minutes. The mixture was washed with brine (30mL) and the aqueous layer was extracted with CH2C12 (2 x 30 mL). The combined organic layers were dried over Na2S04 and concentrated in vacuo, resulting in l-fluoro-2-(fluoromethyl)-4-nitro- benzene (3.9 g). A mixture of l-fluoro-2-(fluoromethyl)-4-nitro-benzene (3.1 g, 17.9 mmol), iron (4.0 g, 71.6 mmol) and methanol (30 mL) was stirred at 65° for 8 hours. The mixture was filtrated and the filtrate was concentrated in vacuo, resulting in 4-fluoro-3-(fluoromethyl)aniline (1.5 g). 3-(chlorosulfonyl)benzoyl chloride (300 mg, 1.2 mmol) and triethylamine (150 mg, 1.5 mmol) were dissolved in dichloromethane (20 mL). 4-fluoro-3-(fluoromethyl)aniline (175 mg, 1.22 mmol) was added to the mixture at 0° C. The mixture was stirred at 10°C for 30 minutes. The mixture was used to the next step without further purification.Triethylamine (152 mg, 1.5 mmol) and 3-methyl-3-oxetanamine (131 mg. 1.5 mmol) were added to the above obtained reaction mixture at 0° C. The mixture was stirred at 20° C for 1 hour. The solvent was removed in vacuo and the obtained residue was purified by reversed phase high performance liquid chromatography (Column: Gemini 250*20mm*5um.. A:
H2O+0.1%TFA B: MeCN. 27% to 57% B in A). The product fractions were collected and the organic solvent was removed in vacuo. The fraction was neutralized by saturated NaHC03. The mixture was extracted with dichloromethane (3 x 20 mL) and the combined organic layer was dried over Na2S04 and concentrated in vacuo, resulting in compound 127 (91.1 mg). Method A; Rt: 4.95 min. m/z : 397.3 (M+H)+ Exact mass: 396.1. 1H NMR (400 MHz, DMSO-d6) δ ppm 1.41 (s, 3 H) 4.14 (d, J=6.3 Hz, 2 H) 4.56 (d, J=6.3 Hz, 2 H) 5.52 (d, J=48 Hz, 2 H) 7.31 (t, J=9.4 Hz, 1 H) 7.72 - 7.89 (m, 2 H) 7.92-7.97 (m, 1 H) 8.03 (d, J=8.0 Hz, 1 H) 8.23 (d, J=7.8 Hz, 1 H) 8.39 (s, 1 H) 8.55 (s, 1 H) 10.67 (s, 1 H).
Compound 112
Figure imgf000071_0001
Compound 123 (255 mg, 0.592 mmol) and Pd/C (50 mg) were stirred in methanol (25 mL) under a hydrogen atmosphere for 3 hours. The reaction mixture was filtered, concentrated and the obtained residue dried in vacuo at 50°C resulting in compound 112 as a colorless resin.(174 mg). Method G; Rt: 1.57 min. m/z : 397.1 (M+H)+ Exact mass: 396.1. 1H NMR (400 MHz, DMSO-d6) δ ppm 1.65 - 1.80 (m, 1 H), 1.91 - 2.04 (m, 1 H), 2.24 (d, J=1.5 Hz, 3 H), 3.43 (dd, J=9.0, 4.6 Hz, 1 H), 3.55 - 3.79 (m, 3 H), 3.80 - 3.91 (m, 1 H), 7.14 (t, j=9.2 Hz, 1 H), 7.45 - 7.57 (m, 2 H), 7.64 (dd, J=7.0, 2.4 Hz, 1 H), 7.85 - 8.02 (m, 2 H), 8.40 (d, J=6.8 Hz, 1 H), 10.62 (s, 1 H)
Compound 113
Figure imgf000071_0002
3-methyloxetan-3-amine hydrochloride (210 mg, 1.7 mmol) and NaOH (204 mg, 5.1 mmol) were dissolved in 2-methyltetrahydrofuran (5 mL) and H20 (5 mL).
5-chlorosulfonyl-2-methyl-benzoic acid (400 mg, 1.7 mmol) was added at 0°C. The mixture was stirred at 20°C for 4 hours. The aqueous layer was separated and adjusted to pH=3 by aq.HCl (IN). The mixture was extracted with ethyl acetate (3 x 100 mL). The combined organic layers were concentrated in vacuo resulting in 2-methyl-5- [(3-methyloxetan-3-yl)sulfamoyl]benzoic acid (250 mg). 2-methyl-5-[(3-methyloxetan- 3-yl)sulfamoyl]benzoic acid (250 mg, 0.876 mmol), 3-(difluoromethyl)-4-fluoro- aniline (178 mg, 1.1 mmol) and DIPEA (232 mg, 1.8 mmol) were dissolved in DMF (5 mL). HATU (399 mg , 1.05 mmol) was added at 0°C. The mixture was stirred at 20°C for 2 hours. The solvent was removed in vacuo and the obtained residue was purified by reversed phase high performance liquid chromatography (mobile phase: CH3CN in water (0.1% TFA) from 34% to 64%). The pure fractions were collected and neutralized with solid NaHCOs. The organic solvent was removed in vacuo and the formed precipitate was filtered, washed with H20 (5 mL) and dried under high vacuum. The residue was suspended in water (5 mL) and the aqueous layer was lyophilized to dryness resulting in compound 113 (220 mg). Method A; Rt: 5.28 min. m/z : 429.3 (M+H)+ Exact mass: 428.1. 1H NMR (400 MHz, DMSO-d6) δ ppm 1.44 (s, 3 H) 2.47 (s, 3 H) 4.15 (d, J=6.3 Hz, 2 H) 4.57 (d, J=6.0 Hz, 2 H) 7.24 (t, J=54.5 Hz, 1 H) 7.40 (t, J=9.5 Hz, 1 H) 7.56 (d, J=8.0 Hz, 1 H) 7.71 - 7.98 (m, 3 H) 8.09 (d, J=4.3 Hz, 1 H) 8.37 (br. s., 1 H) 10.74 (br. s., 1 H)
Compound 114
Figure imgf000072_0001
3-(isopropylsulfamoyl)benzoic acid (190 mg, 0.78 mmol) was dissolved in
dichloromethane (5 mL). 3-fluoro-4-methoxyaniline (139 mg, 0.94 mmol) and triethylamine (112 mg, 1 mmol) were added to the mixture at 20°C. The mixture was stirred at 20°C for 5 minutes. HATU (358 mg, 0.94 mmol) was added to the mixture at 20°C. The mixture was stirred at 20°C for 8 hours. The solvent was removed in vacuo and the obtained residue was purified by high performance liquid chromatography (Column: Phenomenex Synergi C18 150*20mm*5um.. A: H2O+0.1%TFA B: MeCN 30%) to 60%) B in A). The product fractions were collected and the organic solvent was evaporated. The aqueous layer was neutralized with saturated aqueous NaHC03. The mixture was extracted with dichloromethane (2 x 10 mL). The combined organic layers were dried over Na2S04 and concentrated in vacuo resulting in compound 114
(135 mg). Method A; Rt: 5.60 min. m/z: 367.2 (M+H)+ Exact mass: 366.1
Compound 115
Figure imgf000072_0002
Prepared similarly as desribed for compound 127 using 4-fluoro-2,3-dimethyl-aniline instead of 4-fluoro-3-(fluoromethyl)aniline. Method A; Rt: 4.98 min. m/z : 393.3 (M+H)+ Exact mass: 392.1.
Compound 116
Figure imgf000073_0001
4-fluoro-3 -methyl-aniline (9.04 g, 72.2 mmol) was added drop wise to a solution of 3-(chlorosulfonyl) benzoyl chloride (19.0g, 79.47 mmol) in toluene (300 mL) at 110°C. The resultant mixture was stirred at 110°C for 1 hour and allowed to cool to 20°C overnight. The precipitate was filtered and recrystallized from dry toluene resulting in 3-[(4-fluoro-3-methyl-phenyl)carbamoyl]benzenesulfonyl chloride (20 g). 3-[(4-fluoro- 3-methyl-phenyl)carbamoyl]benzenesulfonyl chloride (15 g, 45.77 mmol) was added drop wise at 0°C to a solution of 2-aminopropan-l-ol (3.437 g, 45.77 mmol) and triethylamine (6.946 g) in THF (200 mL). The resultant mixture was stirred for 10 minutes and then allowed to warm to 20°C during 2 hours. The reaction mixture was quenched with IN HCl (50 mL). The mixture was extracted with dichloromethane (3 x 30 mL).The combined organic layers were washed with brine, dried over MgSC^, filtered and concentrated in vacuo. The residue was purified by silica gel column chromatography (gradient eluent: petroleum ether / ethyl acetate from 100/1 to 50/50), resulting in N-(4-fluoro-3-methyl-phenyl)-3-[(2-hydroxy- 1 -methyl-ethyl)sulfamoyl]- benzamide (15.6 g). Diethyl diazene-l,2-dicarboxylate (4.91 g, 28.19 mmol) was added drop wise to a solution of N-(4-fluoro-3-methyl-phenyl)-3-[(2-hydroxy-l-methyl- ethyl)sulfamoyl]benzamide (7.8 g, 21.29 mmol) and PPh3 (6.14 g, 23.41 mmol) in THF (500 mL) at -70°C under Argon. The resultant mixture was stirred for 1 hour and then allowed to warm to 20°C overnight. The reaction mixture was quenched with IN HCl (300 mL). The mixture was extracted with dichloromethane (4 x 400 mL) and the combined organic layers were washed with brine, dried over MgSC^, filtered and concentrated in vacuo. The obtained residue was purified by silica gel column chromatography (gradient eluent: petroleum ether / ethyl acetate from 100/1 to 60/40) resulting in N-(4-fluoro-3-methyl-phenyl)-3-(2-methylaziridin- 1 -yl)sulfonyl-benzamide (6.5 g). A mixture of N-(4-fluoro-3-methyl-phenyl)-3-(2-methylaziridin-l-yl)sulfonyl- benzamide (300 mg, 0.861 mmol) and 1-methylpiperazine (862 mg, 8.61 mmol) in 1.4-dioxane (3 mL) was heated by microwave irradiation at 150°C for 30 minutes. The volatiles were removed in vacuo. The obtained residue was purified by silica gel column chromatography (gradient eluent: petroleum ether/ethyl acetate from 100/1 to 1/100). The pure fractions were collected and the solvent was removed in vacuo. The obtained residue was purified by preparative high-performance liquid chromatography (column: Luna 150*30mm*5u, mobile phase: CH3CN in water (0.1% NH4HCO3) from 44%) to 74%)). The pure fractions were collected, concentrated in vacuo and the residual aqueous solution was lyophilized to dryness resulting in compound 116 (250 mg). Method A; Rt: 4.26 min. m/z : 449.4 (M+H)+ Exact mass: 448.2
Compound 117
Figure imgf000074_0001
Prepared similarly as desribed for compound 116 using morpholine instead of
1-methylpiperazine. Method A; Rt: 4.45 min. m/z : 436.3 (M+H)+ Exact mass:
Compound 118
Figure imgf000074_0002
To a stirred solution of 3,4-difluoro-2-methyl-aniline (369 mg, 2.6 mmol), 3-[[(35)- tetrahydrofuran-3-yl]sulfamoyl]benzoic acid (700 mg, 2.58 mmol) and N,N- diisopropylethylamine(1.35 ml, 7.74 mmol) in DMF (10 mL), Pybrop (132705-51-2, 1.82 g, 3.9 mmol) was added at 0° C. The resulting mixture was stirred overnight at 18 °C. The mixture was concentrated in vacuo, ethyl acetate (15 mL) was added and the organic layer was washed with IN HC1 (15 ml) and saturated aqueous NaHC03 (15 mL). After drying over Na2S04 and concentration in vacuo, the crude residue was purified by reversed phase preparative high-performance liquid chromatography
(eluent: CH3CN in H20 (0.05% NH3.H20) from 37% to 37%, v/v). The pure fractions were collected and the volatiles were removed in vacuo. The aqueous layer was lyophilized to dryness, resulting in compound 118 (238 mg). Method D; Rt: 5.01 min. m/z : 396.9 (M+H)+ Exact mass: 396.1
Compound 119
Figure imgf000074_0003
Prepared similarly as described for compound 127 using 4-fluoro-2,5-dimethyl-aniline instead of 4-fluoro-3-(fluoromethyl)aniline, and DIPEA instead of NEt3. Method A; Rt: 5.27 min. m/z: 393.3 (M+H)+ Exact mass: 392.1
Compound 120
Figure imgf000075_0001
A mixture of l-(2-pyridyl)propan-2-amine (207.8 mg, 1.53 mmol) and DIPEA
(0.532 mL, 3.05 mmol) were dissolved in CH2CI2 (10 mL). 3-[(4-fluoro-3-methyl- phenyl)carbamoyl]benzenesulfonyl chloride (500 mg, 1.53 mmol) was added portion wise at 0°C and the mixture was stirred at 0°C for 1 hour. The mixture was washed with saturated citric acid (10 mL), saturated aqueous NaHC03 (10 mL), brine and dried over Na2S04. The solvent was removed in vacuo and the obtained residue was purified by silica gel column chromatography (gradient eluent: petroleum ether/ethyl acetate from 100/1 to 1/100). The pure fractions were collected and the solvent was removed in vacuo. The obtained solid was suspended in water (10 mL) and acetonitrile (10 mL) and the solution was lyophilized to dryness resulting in compound 120 (550 mg).
Method B; Rt: 3.36 min. m/z: 428.3 (M+H)+ Exact mass: 427.1. 1H NMR (400 MHz, DMSO-dg) δ ppm 0.95 (d, J=6.5 Hz, 3 H) 2.26 (d, J=1.5 Hz, 3 H) 2.69 (dd, J=13.6, 7.3 Hz, 1 H) 2.80 (dd, J=13.6, 7.0 Hz, 1 H) 3.64 - 3.74 (m, 1 H) 7.08 - 7.19 (m, 3 H) 7.55- 7.64 (m, 2 H) 7.64 - 7.71 (m, 2 H) 7.84 - 7.89 (m, 1 H) 7.89 - 7.95 (m, 1 H) 8.12 - 8.17 (m, 1 H) 8.25 (t, J=1.5 Hz, 1 H) 8.32 - 8.36 (m, 1 H) 10.45 (s, 1 H).
Compound 224
Figure imgf000075_0002
Compound 224 was prepared similarly as described for compound 223, using l-(4- pyridyl)propan-2-amine instead of l-(2-pyridyl)propan-2-amine. Compound 224 was purified by preparative high-performance liquid chromatography (column: Luna 150*30mm*4u, mobile phase: CH3CN in water (0.05% NH4HC03) from 40% to 70%). Method A; Rt: 4.6 min. m/z: 428.3 (M+H)+ Exact mass: 427.1.
Synthesis of 5-chlorosulfonyl-2-methyl-benzoyl chloride and 3-[(4-fluoro-3-methyl- phenyDcarbamoyl] -4-methyl-benzenesulfonyl chloride 5-(chlorosulfonyl)-2-methylbenzoic acid (10 g, 42.61 mmol) was dissolved in dichloromethane (200 mL). N,N-dimethylformamide (166 μί, 2.13 mmol) was added and the mixture was stirred at room temperature under a nitrogen atmosphere.
Oxalyl chloride (18.3 mL, 213 mmol) was added in four portions over one hour.
The resulting mixture was stirred for one hour at room temperature. The mixture was concentrated in vacuo and co-evaporated twice using toluene (2 x 100 mL) yielding 5- chlorosulfonyl-2-methyl-benzoyl chloride as a yellow oil which was used as such. 5- chlorosulfonyl-2-methyl-benzoyl chloride_(10.7 g, 42.3 mmol) was dissolved in toluene (220 mL) and this was heated to reflux and stirred under a gentle flow of nitrogen. 4-f uoro-3-methylaniline (4.76 g, 38.1 mmol) in toluene (80 mL) was added drop wise using a syringe pump (0,8 mL / min). The resulting mixture was stirred for 30 minutes while heating was continued. Then the mixture was cooled to room temperature. A precipitation was formed and collected on a glass filter. The obtained solid was dried in vacuo at 55°C, yielding 3-[(4-fluoro-3-methyl-phenyl)carbamoyl]-4-methyl- benzenesulfonyl chloride (10.4 g) as a solid which was used as such in the next step.
Compound 121
Figure imgf000076_0001
A solution of (5)-3-aminotetrahydrofuran tosylate (0.76 g, 2.93 mmol) and
diisopropylethylamine (1.26 mL, 7.31 mmol) in dichloromethane (10 mL) was added drop wise to a solution of 3-[(4-fluoro-3-methyl-phenyl)carbamoyl]-4-methyl- benzenesulfonyl chloride (1 g, 2.93 mmol) in dichloromethane (10 mL). The resulting mixture was stirred for 1 hour at room temperature. The mixture was quenched using HC1 (aq / 14.6 mL, 14.6 mmol). The layers were separated and the water layer was extracted with dichloromethane (2 x 20 mL). The combined organics were concentrated in vacuo and purified using silica gel column chromatography (gradient elution:
EtO Ac-heptane 0: 100 to 100:0). The desired fractions were concentrated in vacuo and dried in vacuo at 55°C yielding compound 121 as a bright white solid. Method F; Rt: 0.90 min. m/z: 393.2 (M+H)+ Exact mass: 392.1. 1H NMR (400 MHz, DMSO-d6) δ ppm 1.58 - 1.69 (m, 1 H), 1.85 - 1.98 (m, 1 H), 2.24 (d, J=1.3 Hz, 3 H), 2.45 (s, 3 H), 3.38 (dd, J=8.8, 4.4 Hz, 1 H), 3.53 - 3.65 (m, 2 H), 3.66 - 3.76 (m, 2 H), 7.13 (t, J=9.2 Hz, 1 H), 7.46 - 7.59 (m, 2 H), 7.66 (dd, J=7.0, 2.2 Hz, 1 H), 7.75 - 7.87 (m, 2 H), 7.96 (br. s., 1 H), 10.46 (s, 1 H). Compound 122
Figure imgf000077_0001
A solution of 3-methyl-3-oxetanamine hydrochloride (0.4 g, 3.22 mmol) and diisopropylethylamine (1.26 mL, 7.31 mmol) in of dichloromethane (10 mL) was added drop wise to a solution of 3-[(4-fluoro-3-methyl-phenyl)carbamoyl]-4-methyl- benzenesulfonyl chloride (1 g, 2.93 mmol) in dichloromethane(10 mL). The resulting mixture was stirred for 1 hour at room temperature. The mixture was quenched using HC1 (aq / 14.63 mL, 14.63 mmol). The layers were separated and the water layer was extracted using dichloromethane (2 x 20 mL). The combined organic layers were concentrated in vacuo and purified using column chromatography (gradient elution: EtO Ac-heptane 0: 100 to 100:0). The desired fractions were concentrated in vacuo and dried in a vacuum oven at 55°C yielding compound 122 as a bright white solid. Method
F; Rt: 0.90 min. m/z: 410.2 (M+NH4)+ Exact mass: 392.1.1H NMR (400 MHz, DMSO- d6) δ ppm 1.43 (s, 3 H), 2.19 - 2.29 (m, 3 H), 2.44 (s, 3 H), 4.14 (d, J=6.4 Hz, 2 H), 4.56 (d, J=6.2 Hz, 2 H), 7.13 (t, J=9.1 Hz, 1 H), 7.42 - 7.57 (m, 2 H), 7.59 - 7.71 (m, 1 H), 7.74 - 7.90 (m, 2 H), 8.36 (s, 1 H), 10.46 (s, 1 H).
Compound 123
Figure imgf000077_0002
Compound 123 was prepared similarly as described for compound 121 starting from 5-chloro-3-chlorosulfonyl-2-fluoro-benzoic acid (commercial from Enamine EN300- 35191) via 5-chloro-3-chlorosulfonyl-2-fiuoro-benzoyl chloride (1H NMR (400 MHz, CHLOROFORM-d) δ ppm 8.23 (dd, J=5.4, 2.8 Hz, 1 H), 8.37 (dd, J=5.5, 2.6 Hz, 1 H)). After silica gel column chromatography (gradient elution: EtO Ac-heptane 10:90 to 100:0) compound 123 was crystallised by addition of H20 to a hot iPrOH solution of compound 123, resulting in compound 123 as white solid (3153 mg). Method G; Rt: 1.81 min. m/z: 431.0 (M+H)+ Exact mass: 430.1. 1H NMR (400 MHz, DMSO-d6) δ ppm 1.65 - 1.79 (m, 1 H), 1.93 - 2.06 (m, 1 H), 2.25 (d, J=1.8 Hz, 3 H), 3.44 (dd, J=9.0, 4.4 Hz, 1 H), 3.62 (td, J=8.0, 5.9 Hz, 1 H), 3.69 (dd, J=8.9, 6.3 Hz, 1 H), 3.71 - 3.79 (m, 1 H), 3.84 - 3.98 (m, 1 H), 7.15 (t, J=9.1 Hz, 1 H), 7.45 - 7.55 (m, 1 H), 7.61 (dd, J=6.9, 2.3 Hz, 1 H), 7.91 (dd, J=5.7, 2.6 Hz, 1 H), 8.07 (dd, J=5.2, 2.8 Hz, 1 H), 8.57 (d, J=6.8 Hz, 1 H), 10.68 (s, 1 H)
Compound 124
Figure imgf000078_0001
Compound 125 (167 mg,0.371 mmol) and Pd/C (25 mg) were stirred in methanol (19 mL) under hydrogen atmosphere during 80 minutes. The reaction mixture was filtered and concentrated. The obtained residue was purified by preparative SFC (Stationary phase: Chiralpak Diacel AD 30 x 250 mm), Mobile phase: C02, MeOH with 0.2% iPrNH2), the desired fractions were collected, evaporated, dissolved in MeOH and evaporated again resulting in compound 124 (67 mg). Method G; Rt: 1.61 min. m/z: 430.0 (M+NH4)+ Exact mass: 412.1. 1H NMR (400 MHz, DMSO-d6 ) δ ppm 1.68 - 1.83 (m, 1 H), 1.89 - 2.03 (m, 1 H), 2.24 (d, J=1.5 Hz, 3 H), 3.45 (dd, J=8.9, 4.7 Hz, 1 H), 3.56 - 3.69 (m, 2 H), 6 3.70 - 3.86 (m, 2 H), 7.14 (t, J=9.1 Hz, 1 H), 7.45 - 7.55 (m, 1 H), 7.60 - 7.69 (m, 2 H), 7.82 (dd, J=7.6, 1.7 Hz, 1 H), 8.09 (dd, J=7.8, 1.7 Hz, 1 H), 8.34 (s, 1 H), 10.62 (s, 1 H)
Compound 125
Figure imgf000078_0002
Compound 125 was prepared similarly as described for compound 126 starting from 2,6-dichloro-3-chlorosulfonyl-benzoic acid instead of 3-chlorosulfonyl-2-methyl- benzoic acid. Method G; Rt: 1.77 min. m/z: 464.0 (M+NH4) Exact mass: 446.0.
1H NMR (400 MHz, CHLOROFORM-;/) δ ppm 1.75-1.86 (m, 1 H), 2.04 - 2.16 (m, 1 H), 2.30 (d, J=1.8 Hz, 3 H), 3.57 - 3.65 (m, 1 H), 3.66 - 3.76 (m, 2 H), 3.82 - 3.95 (m, 2 H), 5.45 (d, J=7.5 Hz, 1 H), 7.01 (t, J=8.9 Hz, 1 H), 7.30 - 7.38 (m, 1 H), 7.47 - 7.56 (m, 2 H), 7.83 (s, 1 H), 8.05 (d, J=8.6 Hz, 1 H).
Compound 126
Figure imgf000078_0003
3-chlorosulfonyl-2-methyl-benzoic acid (commercial from Enamine EN300-109516; 508.4 mg, 2.17 mmol) was dissolved in dichloromethane (50 mL). DMF (1 drop) and oxalylchloride (1375mg, 10.83 mmol) were added and the mixture was stirred for 4 hours under an inert atmosphere. The reaction mixture was concentrated resulting in 3- chlorosulfonyl-2-methyl-benzoyl chloride as a yellow oil (554 mg) which was used as such in the next step. 1H NMR (400 MHz, CHLOROFORM-;/) δ ppm 2.92 - 3.01 (m, 3 H), 7.60 (t, J=7.9 Hz, 1 H), 8.27 - 8.41 (m, 2 H). 4-Fluoro-3-methylaniline (227 mg, 1.98 mmol) dissolved in dichloromethane (10 mL) was added drop wise, over 5 minutes, to a solution of 3-chlorosulfonyl-2-methyl-benzoyl chloride (550 mg,
2.17 mmol) in toluene (50 mL) at reflux. The reaction mixture was refluxed for 30 minutes and next cooled in an icebath. A solution of (S)-3-aminotetrahydrofuran tosylate (564 mg, 2.17 mmol) and DIPEA (0.85 ml, 4.94 mmol) dissolved in
dichloromethane (10 mL) was added and the obtained mixture was stirred for 30 minutes. The resulting mixture was washed with HC1 (2 x 100 mL / 1M aq), water (2 x 100 mL) and NaHC03 (2 x 100 mL / sat. aq). The organic layer was dried over MgS04, filtered and concentrated in vacuo. The obtained residue was purified using silica gel column chromatography (CH2Cl2-MeOH 100:0 to 90: 10) and repurified by applying a gradient from 10 till 100% EtOAc in heptane. The product fractions were concentrated and dried overnight in vacuo at 50°C yielding compound 126 as colourless oil
(16.6 mg). Method G; Rt: 1.65 min. m/z: 393.1 (M+H)+ Exact mass: 392.1. 1H NMR (400 MHz, CHLOROFORM-^) δ ppm 1.73 - 1.87 (m, 1 H), 2.06 - 2.20 (m, 1 H), 2.30 (d, J=1.8 Hz, 3 H), 2.69 (s, 3 H), 3.54 - 3.63 (m, 1 H), 3.65 - 3.78 (m, 2 H), 3.83 - 3.97 (m, 2 H), 4.99 (d, J=8.1 Hz, 1 H), 7.01 (t, j=8.9 Hz, 1 H), 7.31 - 7.44 (m, 2 H), 7.51 (dd, J=6.7, 2.5 Hz, 1 H), 7.58 - 7.69 (m, 2 H), 8.06 (dd, J=8.0, 1.2 Hz, 1 H)
Procedure SI: A solution of 3-[(4-fluoro-3-methyl-phenyl)carbamoyl]benzenesulfonyl chloride (0.50 g, 1.52 mmol, 1 eq) in toluene (10 mL) was added to a flask containing an amine (1.1 eq). DIPEA (657 μί, 3.81 mmol, 2.5 eq) was added and the reaction mixture was stirred for 1 hour. Next, 1M HC1 (5 mL) was added to the reaction mixture.
Procedure S2: A tube was charged with 3-[(4-fluoro-3-methyl-phenyl)carbamoyl]- benzenesulfonyl chloride (250 mg, 0.76 mmol) and an amine (1.1 eq) and CH2C12 (5 mL) was added. The solution was stirred, DIPEA (329 μί, 1.9 mmol, 2.5 eq) was added and the mixture was further stirred for 30 minutes. Then, HC1 (1M aq / 5 mL) was added and the mixture was stirred for 5 minutes more.
Procedure S3: To a solution of 3-[(4-fluoro-3-methyl-phenyl)carbamoyl]benzene- sulfonyl chloride (0.50 g, 1.52 mmol, 1 eq) and DIPEA (657 μί, 3.81 mmol, 2.5 eq) in CH2CI2 (10 mL), an amine (1.1 eq) was added. The reaction mixture was stirred for 1 hour. Next, 1M HC1 (5 mL) was added to the reaction mixture.
Procedure S4: 3-[(4-fluoro-3-methyl-phenyl)carbamoyl]benzenesulfonyl chloride (250 mg, 0.76 mmol) and DIPEA (329 μί, 1.9 mmol, 2.5 eq) dissolved in CH2C12 (5 mL) were added to a tube containing an amine (1.1 eq). The reaction mixture was stirred for 3 hours. 1M HC1 (5 mL) was added.
Workup Wl: A precipitate was formed. The precipitate was filtered off , rinced with diisopropylether and dried in a vacuum oven at 55 °C.
Workup W2: The organic layer was separated and concentrated in vacuo. The obtained residue was purified by silica gel column chromatography using a heptane to EtOAc gradient as eluent.
Workup W3: The layers were separated and the organic layer was loaded on a silica gel column for purification (with gradient elution: CH2Cl2-methanol 100:0 to 97:3). Workup W4: The organic layer was separated and loaded on a silica gel column. The mixture was purified using gradient elution from heptane to EtOAc.
Compound 128
Figure imgf000080_0001
Synthesis following procedure S4 with 7-oxabicyclo[2.2.1]heptan-2-amine.
as amine, workup W4. Method F; Rt: 0.94 min. m/z: 422.1 (M+NH4) Exact mass: 404.1.1H NMR (400 MHz, DMSC ¾ ) 6 ppm 1.22 - 1.48 (m, 5 H), 1.68 (dd, J=12.5, 7.9 Hz, 1 H), 2.25 (d, J=1.8 Hz, 3 H), 3.25 - 3.29 (m, 1 H), 4.14 (d, J=4.8 Hz, 1 H), 4.44 (t, J=4.8 Hz, 1 H), 7.14 (t, J=9.2 Hz, 1 H), 7.54 - 7.63 (m, 1 H), 7.68 (dd, J=7.2, 2.3 Hz, 1 H), 7.74 - 7.80 (m, 1 H), 7.86 (d, J=6.8 Hz, 1 H), 7.98 - 8.03 (m, 1 H), 8.20 (dt, J=7.8, 1.4 Hz, 1 H), 8.35 (t, J=1.5 Hz, 1 H), 10.46 (s, 1 H).
Compound 129
Figure imgf000080_0002
Synthesis following procedure S3 with R-(+)-3-aminotetrahydrofuran toluene-4- sulfonate as amine, workup W2.
Method F; Rt: 0.89 min. m/z: 396.1 (M+NH4)+ Exact mass: 378.1. 1 H NMR (400 MHz, DMSO-dg ) ppm 1.56 - 1.65 (m, 1 H), 1.85 - 1.94 (m, 1 H), 2.25 (d, J=1.8 Hz, 3 H), 3.36 (dd, J=9.0, 4.4 Hz, 1 H), 3.52 - 3.65 (m, 2 H), 3.65 - 3.73 (m, 1 H), 3.73 - 3.79 (m, 1 H), 7.14 (t, J=9.2 Hz, 1 H), 7.56 - 7.62 (m, 1 H), 7.67 (dd, J=7.0, 2.3 Hz, 1 H), 7.78 (t, J=7.8 Hz, 1 H), 7.99 - 8.05 (m, 1 H), 8.08 (bs, 1 H), 8.20-8.23(m, 1 H), 8.37 (t, J=1.7 Hz, 1 H), 10.47 (s, 1 H), [«]D = + 5.8 (c 0.61 w/v %, MeOH)
Compound 130
Figure imgf000081_0001
Method F; Rt: 0.95 min. m/z: 424.2 (M+NH4) Exact mass: 406.1.
Synthesis following procedure S3 with racemic trans-2-aminocycloh
hydrochloride as amine, workup W2.
Compound 131
Figure imgf000081_0002
Synthesis following procedure S3 with (15',25)-trans-2-aminocyclohexanol
hydrochloride as amine, workup W2.
Method F; Rt: 0.95 min. m/z: 424.2 (M+NH4)+ Exact mass: 406.1.
1H NMR (400 MHz, DMSO-de) δ ppm 1.01 - 1.23 (m, 4 H), 1.41 - 1.58 (m, 2 H), 1.59
- 1.70 (m, 1 H), 1.71 - 1.83 (m, 1 H), 2.25 (d, J=1.3 Hz, 3 H), 2.77 - 2.90 (m, 1 H), 3.15
- 3.27 (m, 1 H), 4.50 (d, J=4.6 Hz, 1 H), 7.14 (t, J=9.2 Hz, 1 H), 7.54 - 7.64 (m, 2 H), 7.64 - 7.69 (m, 1 H), 7.72 (t, J=7.9 Hz, 1 H), 8.04 (d, J=7.7 Hz, 1 H), 8.16 (d, J=7.9 Hz, 1 H), 8.39 (s, 1 H), 10.43 (s, 1 H)
Compound 132
Figure imgf000081_0003
Synthesis following procedure S3 with racemic cis-2-aminocyclohexanol hydrochloride as amine, workup W2. Method F; Rt: 0.96 min. m/z: 424.1 (M+NH4)+ Exact mass: 406.1. 1H NMR (400 MHz, DMSO-d6 ) δ ppm 1.01 - 1.26 (m, 4 H), 1.26 - 1.36 (m, 1 H), 1.38 - 1.62 (m, 3 H), 2.25 (d, J=1.8 Hz, 3 H), 3.03 - 3.14 (m, 1 H), 3.57 (br. s., 1 H), 4.52 (d, J=4.2 Hz, 1 H), 7.14 (t, J=9.1 Hz, 1 H), 7.46 (d, J=7.9 Hz, 1 H), 7.56 - 7.62 (m, 1 H), 7.68 (dd, J=7.0, 2.6 Hz, 1 H), 7.73 (t, J=7.8 Hz, 1 H), 8.05 (dt, J=8.1, 1.2 Hz, 1 H), 8.14 - 8.19 (m, 1 H), 8.39 (t, J=1.7 Hz, 1 H), 10.43 (s, 1 H) Compound 133
Figure imgf000082_0001
Synthesis following procedure S3 with trans-4-aminocyclohexanol hydrochloride as amine, workup W2.
Method F; Rt: 0.84 min. m/z: 424.2 (M+NH4)+ Exact mass: 406.1.
1 H NMR (400 MHz, DMSO-d6) δ ppm 1.01 - 1.31 (m, 4 H), 1.57 (d, J=10.3 Hz, 2 H), 1.69 (d, J=12.5 Hz, 2 H), 2.25 (d, J=1.8 Hz, 3 H), 2.84 - 3.01 (m, 1 H), 3.22 - 3.29 (m, 1 H), 4.46 (d, J=4.4 Hz, 1 H), 7.14 (t, J=9.1 Hz, 1 H), 7.53 - 7.64 (m, 1 H), 7.68 (dd, J=7.0, 2.2 Hz, 1 H), 7.72 - 7.79 (m, 2 H), 7.95 - 8.04 (m, 1 H), 8.18 (dt, J=7.7, 1.3 Hz, 1 H), 8.36 (t, J=1.7 Hz, 1 H), 10.46 (s, 1 H)
Compound 134
Figure imgf000082_0002
Method F; Rt: 0.89 min. m/z: 424.2 (M+NH4) Exact mass: 406.1.
Synthesis following procedure S3 with 3-amino-cyclohexanol as amine, workup W2.
Compound 134 was separated in it's isomers by preparative SFC (Stationary phase: Chiralpak Daicel IC 20 x 250 mm), Mobile phase: C02, iPrOH with 0.4% iPrNH2), the desired fractions were collected, evaporated, dissolved in MeOH and evaporated again, yielding 134a, 134b, 134c, 134d. SFC Columns: ID-H 250 mm x 4.6 mm Flow: 3 ml/min Mobile phase: 25 % iPrOH (containing 0.2% iPrNH2) hold 18.0 min.
Temperature: 30°C; Rt: 134 a (10.0 min), 134b (11.1 min), 134c (13.6 min), 134d
(14.7 min). Cis: Enantiomers 134a and 134b N-(4-fluoro-3-methyl-phenyl)-3- [[(lR,3S)-3-hydroxycyclohexyl]sulfamoyl]benzamide or N-(4-fluoro-3-methyl- phenyl)-3-[[(lS,3R)-3-hydroxycyclohexyl]sulfamoyl]benzamide. 1H NMR (400 MHz, DMSO-de ) δ ppm 0.84 - 1.14 (m, 4 H), 1.48 - 1.60 (m, 2 H), 1.60-1.72 (m, 1 H), 1.72 - 1.82 (m, 1 H), 2.26 (d, J=1.8 Hz, 3 H), 2.93 - 3.07 (m, 1 H), 3.20 - 3.30 (m, 1 H), 4.58 (d, J=4.6 Hz, 1 H), 7.14 (t, J=9.1 Hz, 1 H), 7.55 - 7.64 (m, 1 H), 7.69 (dd, J=7.0, 2.2
Hz, 1 H), 7.76 (t, J=7.8 Hz, 1 H), 7.83 (br. s., 1 H), 7.96 - 8.06 (m, 1 H), 8.13 - 8.24 (m, 1 H), 8.38 (t, J=1.7 Hz, 1 H), 10.47 (s, 1 H)
Trans: enantiomers 134c and 134d N-(4-fluoro-3-methyl-phenyl)-3-[[(lR,3R)-3 hydroxycyclohexyl]sulfamoyl]benzamide or N-(4-fluoro-3-methyl-phenyl)-3- [[(1 S,3S)-3-hydroxycyclohexyl]sulfamoyl]benzamide 1H NMR (400 MHz, DMSO-d6 ) δ ppm 1.08 - 1.20 (m, 1 H), 1.25 - 1.42 (m, 4 H), 1.42 - 1.58 (m, 3 H), 2.25 (d, J=1.8 Hz, 3 H), 3.36 - 3.45 (m, 1 H), 3.71 - 3.89 (m, 1 H), 4.38 (d, J=3.5 Hz, 1 H), 7.14 (t, J=9.1 Hz, 1 H), 7.51 (br. s., 1 H), 7.56 - 7.63 (m, 1 H), 7.69 (dd, J=7.2, 2.3 Hz, 1 H), 7.73 - 7.78 (m, 1 H), 7.97 - 8.05 (m, 1 H), 8.19 (dt, J=7.9, 1.2 Hz, 1 H), 8.37 (t, J=1.7 Hz, 1 H), 10.47 (br. s., 1 H)
Compound 135
Figure imgf000083_0001
Synthesis following procedure S3 with 2-oxa-6-azaspiro[3.3]heptane as amine, workup W2. Method F; Rt: 0.91 min. m/z: 389.1 (M-H)~ Exact mass: 390.1. 1H NMR (400 MHz, DMSO-dg ) δ ppm 2.26 (d, J=1.8 Hz, 3 H), 3.95 (s, 4 H), 4.44 (s, 4 H), 7.15 (t, j=9.2 Hz, 1 H), 7.57 - 7.65 (m, 1 H), 7.68 (dd, J=7.0, 2.4 Hz, 1 H), 7.85 (t, j=7.8 Hz, 1 H), 8.01 (dt, j=8.0, 1.3 Hz, 1 H), 8.28 - 8.38 (m, 2 H), 10.51 (s, 1 H).
Compound 136
Figure imgf000083_0002
Synthesis following procedure SI with (li?,25)-(+)-cis-l-aminoindan-2-ol as amine, workup Wl . Method G; Rt: 1.79 min. m/z: 439.0 (M-H)" Exact mass: 440.1. 1 H NMR (400 MHz, DMSO-dg) δ ppm 2.25 (d, J=1.8 Hz, 3 H), 2.72 (d, J=15.0 Hz, 1 H), 2.93 (dd, J=16.1, 4.6 Hz, 1 H), 4.15 (qd, J=4.7, 1.8 Hz, 1 H), 4.69 (dd, J=8.7, 4.7 Hz, 1 H), 4.96 (d, J=4.4 Hz, 1 H), 6.87 (d, J=7.3 Hz, 1 H), 7.04 - 7.10 (m, 1 H), 7.10 - 7.21 (m, 3 H), 7.55 - 7.64 (m, 1 H), 7.68 (dd, J=7.0, 2.4 Hz, 1 H), 7.77 (t, j=7.8 Hz, 1 H), 7.93 (d, J=9.0 Hz, 1 H), 8.15 (dt, j=8.1, 1.2 Hz, 1 H), 8.21 (dd, J=7.7, 1.5 Hz, 1 H), 8.48 (t, j=1.7 Hz, 1 H), 10.44 (s, 1 H)
Compound 137
Figure imgf000083_0003
Synthesis following procedure S4 with (15',2i?)-2-aminotetralin-l-ol hydrochloride as amine, workup W4. Method F; Rt: 1.03 min. m/z: 472.2 (M+NH4) Exact mass: 454.1. 1H NMR (400 MHz, DMSO-dg ) δ ppm 1.35 - 1.46 (m, 1 H), 1.96 (qd, J=l 1.8, 6.2 Hz, 1 H), 2.25 (d, J=1.5 Hz, 3 H), 2.62 (ddd, J=17.2, 10.9, 6.3 Hz, 1 H), 2.70 - 2.82 (m, 1 H), 3.34 - 3.45 (m, 1 H), 4.39 (br. s., 1 H), 5.29 (d, J=5.7 Hz, 1 H), 7.04 (d, J=6.8 Hz, 1 H), 7.09 - 7.24 (m, 4 H), 7.55 - 7.63 (m, 1 H), 7.62-7.70 (m, 2 H), 7.75 (t, J=7.8 Hz, 1 H), 8.06 - 8.13 (m, 1 H), 8.19 (d, J=8.1 Hz, 1 H), 8.43 (t, J=1.5 Hz, 1 H), 10.44 (s, 1 H), [«]D : +66 ° (c 0.55 w/v %, DMF). DSC (From 30 to 300 °C at 10°C/min):
Figure imgf000084_0001
Synthesis following procedure SI with trans-(15',25)-2-aminocyclopentanol hydrochloride as amine, workup Wl . Method F; Rt: 0.88 min. m/z: 410.4 (M+NH4)+ Exact mass: 392.1. 1 H NMR (400 MHz, DMSO-de) δ ppm 1.16 - 1.29 (m, 1 H), 1.29 - 1.40 (m, 1 H), 1.50 (quin, J=7.4 Hz, 2 H), 1.61 - 1.78 (m, 2 H), 2.25 (d, J=1.8 Hz, 3 H), 3.16 - 3.26 (m, 1 H), 3.74 - 3.82 (m, 1 H), 4.67 (d, J=4.4 Hz, 1 H), 7.14 (t, J=9.2 Hz, 1 H), 7.55 - 7.63 (m, 1 H), 7.65 - 7.72 (m, 2 H), 7.75 (t, J=7.8 Hz, 1 H), 7.98 - 8.04 (m, 1 H), 8.18 (dt, J=7.9, 1.3 Hz, 1 H), 8.36 (t, J=1.7 Hz, 1 H), 10.45 (s, 1 H)
Compound 139
Figure imgf000084_0002
Synthesis following procedure SI with cis-(li?,25)-2-aminocyclopentanol
hydrochloride as amine, workup Wl . Method F; Rt: 0.92 min. m z: 410.1 (M+NH4)+ Exact mass: 392.1. 1 H NMR (400 MHz, DMSO-d6) δ ppm 1.25 - 1.51 (m, 4 H), 1.51 - 1.67 (m, 2 H), 2.25 (d, J=1.5 Hz, 3 H), 3.21 - 3.28 (m, 1 H), 3.72 - 3.79 (m, 1 H), 4.63 (d, J=4.0 Hz, 1 H), 7.14 (t, J=9.2 Hz, 1 H), 7.42 (d, J=8.1 Hz, 1 H), 7.55 - 7.63 (m, 1 H), 7.68 (dd, J=7.3, 2.4 Hz, 1 H), 7.73 (t, J=7.8 Hz, 1 H), 8.06 (dt, J=8.1, 1.2 Hz, 1 H), 8.17 (d, J=8.1 Hz, 1 H), 8.40 (t, J=1.5 Hz, 1 H), 10.43 (s, 1 H)
Compound 172
Figure imgf000084_0003
Synthesis following procedure S2 with cis-(15',2i?)-2-aminocyclopentanol
hydrochloride as amine. The formed precipitate was collected on a glassfilter and rinsed with CH2CI2 (2 x 5 mL). The precipitate was further purified using silica gel column chromatography (gradient elution: EtO Ac-heptane 0: 100 to 100:0). Drying in vacuo at 55°C resulted in compound 172 as a bright white powder. Method G; Rt: 1.65 min. m/z: 392.9 (M+H)+ Exact mass: 392.1. DSC (From 30 to 300 °C at 10°C/min): 145 °C. Compound 173
Figure imgf000085_0001
Synthesis following procedure S4 (reaction time= 20 hours instead of 3 hours) with trans-(li?,2i?)-2-aminocyclopentanol as amine, workup W4. Method F; Rt: 0.87 min. m/z: 410.1 (M+NH4)+ Exact mass: 392.1.
Compound 140
Figure imgf000085_0002
Synthesis following procedure SI with l,l-dioxothiolan-3 -amine hydrochloride as amine, workup Wl . Method F; Rt: 0.85 min. m/z: 444.2 (M+NH4)+ Exact mass: 426.1. 1 H NMR (400 MHz, DMSO-d6) δ ppm 1.90 - 2.04 (m, 1 H), 2.16 - 2.24 (m, 1 H), 2.25 (d, J=1.8 Hz, 3 H), 2.81 (dd, J=13.4, 7.0 Hz, 1 H), 3.08 (ddd, J=13.1, 9.1, 7.5 Hz, 1 H), 3.15 - 3.26 (m, 2 H), 3.94 - 4.06 (m, 1 H), 7.15 (t, J=9.2 Hz, 1 H), 7.55 - 7.63 (m, 1 H), 7.68 (dd, J=7.2, 2.3 Hz, 1 H), 7.79 (t, J=7.8 Hz, 1 H), 8.01 - 8.07 (m, 1 H), 8.23 (dt, J=7.7, 1.3 Hz, 1 H), 8.38 (t, J=1.7 Hz, 1 H), 8.40 (br. s., 1 H), 10.48 (s, 1 H)
Compound
Figure imgf000085_0003
Synthesis following procedure S4 with 2-aminoindan-l-ol hydrochloride
as amine, workup W4. Method F; Rt: 0.98 and 1.01 min. m/z: 458.1 (M+NH4)+ Exact mass: 440.1. Compound 141 was separated in it's isomers by preparative SFC
(Stationary phase: Chiralcel Diacel OD 20 x 250 mm), Mobile phase: C02, MeOH with 0.2% iPrNH2), the desired fractions were collected, evaporated, dissolved in MeOH and evaporated again. SFC, Column: OD-H (Diacel) 250 mm x 4.6 mm
Flow: 5 mL/min, Mobile phase: 30% MeOH (containing 0.2% iPrNH2) hold 4.00 min, up to 50% in 1 min and hold 2.00 min @ 50% Temperature: 40°C.Rt: 141a (1.8 min), 141b (2.1 min), 141c (2.5 min), 141d (2.7 min).
141a, 141c: N-(4-fiuoro-3-methyl-phenyl)-3-[[(lS,2S)-l-hydroxyindan-2-yl]- sulfamoyl]benzamide or N-(4-fluoro-3-methyl-phenyl)-3-[[(lR,2R)-l-hydroxyindan-2- yl]sulfamoyl]benzamide. 1H NMR (400 MHz, DMSO- 6 ) δ ppm 2.25 (d, J=1.5 Hz, 3 H), 2.43-2.55 (m, 1 H), 2.83 (dd, J=15.7, 7.8 Hz, 1 H), 3.59 - 3.70 (m, 1 H), 4.83 (d, J=6.8 Hz, 1 H), 5.58 (br. s., 1 H), 7.03 - 7.27 (m, 5 H), 7.56 - 7.65 (m, 1 H), 7.68 (dd, J=7.0, 2.4 Hz, 1 H), 7.78 (t, J=7.8 Hz, 1 H), 8.05 - 8.11 (m, 1 H), 8.16 (br. s., 1 H), 8.22 (d, J=8.1 Hz, 1 H), 8.43 (t, J=1.7 Hz, 1 H), 10.47 (br. s., 1 H) Method F; Rt: 0.98 m/z: 458.3 (M+NH4)+ Exact mass: 440.1.
141b, 141d: N-(4-fluoro-3-methyl-phenyl)-3-[[(li?,25)-l-hydroxyindan-2- yl]sulfamoyl]benzamide or N-(4-fluoro-3 -methyl-phenyl)-3 - [ [( 1 S ,2R)- 1 -hydroxyindan- 2-yl]sulfamoyl]benzamide. 1H NMR (600 MHz, ACETONE-de, -14 °C) δ ppm 2.25 (d, J=1.9 Hz, 3 H), 2.80 - 2.90 (m, 2 H), 3.94 - 3.99 (m, 1 H), 4.72 (d, J=5.3 Hz, 1 H), 4.87 (d, J=3.8 Hz, 1 H), 6.96 (d, J=5.0 Hz, 1 H), 7.08 (t, J=9.2 Hz, 1 H), 7.14 - 7.19 (m, 2 H), 7.21 (td, J=7.3, 1.2 Hz, 1 H), 7.29 (d, J=7.3 Hz, 1 H), 7.65 - 7.70 (m, 1 H), 7.74 (dt, J=6.8, 3.1 Hz, 1 H), 7.79 (t, J=7.8 Hz, 1 H), 8.19 (ddd, J=7.8, 1.8, 1.1 Hz, 1 H), 8.27 (ddt, J=7.8, 1.8, 0.9, 0.9 Hz, 1 H), 8.54 (q, J=1.6 Hz, 1 H), 10.09 (s, 1 H) Method F; Rt: 1.00 m/z: 458.2 (M+NH4)+ Exact mass: 440.1.
Compound 142
Figure imgf000086_0001
Synthesis following procedure S4 with (li?,2i?)-2-amino-l-phenyl-propan-l-ol as amine, workup W4. Method F; Rt: 1.00 min. m/z: 460.1 (M+NH4)+ Exact mass: 442.1. 1H NMR (400 MHz, DMSO-d6) δ ppm 0.76 (d, J=6.8 Hz, 3 H), 2.25 (d, J=1.3 Hz, 3 H), 3.37 - 3.46 (m, 1 H), 4.56 (d, J=4.6 Hz, 1 H), 5.41 (br. s., 1 H), 7.14 (t, J=9.2 Hz, 1 H), 7.18 - 7.23 (m, 1 H), 7.23 - 7.32 (m, 4 H), 7.49 (br. s., 1 H), 7.56 - 7.64 (m, 1 H), 7.64 - 7.72 (m, 2 H), 7.88 - 7.96 (m, 1 H), 8.15 (d, J=7.9 Hz, 1 H), 8.31 (t, J=1.5 Hz, 1 H), 10.42 (s, 1 H).
Compound 143
Figure imgf000086_0002
Synthesis following procedure SI with (li?,25)-(-)-norephedrine as amine, workup Wl Method F; Rt: 1.01 min. m/z: 460.1 (M+NH4)+ Exact mass: 442.1. 1 H NMR
(400 MHz, DMSO-dg ) δ ppm 0.79 (d, J=6.8 Hz, 3 H), 2.25 (d, J=1.8 Hz, 3 H), 3.33 - 3.37 (m, 1 H), 4.48 (t, J=4.6 Hz, 1 H), 5.42 (d, J=4.6 Hz, 1 H), 7.10 - 7.27 (m, 6 H), 7.55 - 7.63 (m, 1 H), 7.64 - 7.71 (m, 2 H), 7.78 (d, J=8.4 Hz, 1 H), 7.91 (dt, J=8.2, 1.2 Hz, 1 H), 8.12 - 8.18 (m, 1 H), 8.30 (t, J=1.7 Hz, 1 H), 10.42 (s, 1 H) Compound 144
Figure imgf000087_0001
Synthesis following procedure SI with (IS, 2i?)-(+)-norephedrine as amine, workup Wl . Method F; Rt: 1.01 min. m/z: 460.2 (M+NH4)+ Exact mass: 442.1.
1H NMR (400 MHz, DMSO-de) δ ppm 0.79 (d, J=6.8 Hz, 3 H), 2.25 (d, J=1.8 Hz, 3 H), 3.32 - 3.38 (m, 1 H), 4.48 (t, J=4.6 Hz, 1 H), 5.42 (d, J=4.8 Hz, 1 H), 7.10 - 7.27 (m, 6 H), 7.56 - 7.63 (m, 1 H), 7.65 - 7.71 (m, 2 H), 7.78 (d, J=8.4 Hz, 1 H), 7.89 - 7.94 (m, 1 H), 8.15 (dt, J=7.8, 1.3 Hz, 1 H), 8.30 (t, J=1.7 Hz, 1 H), 10.42 (s, 1 H)
Compound 145
Figure imgf000087_0002
Synthesis following procedure S4 with 3-aminocyclopentanol as amine, after completion, the reaction mixture was directly loaded on a silica gel column for purification, using a heptane to EtOAc gradient yielding compound 145 as a 83 (145a, 145b): 17 (145c, 145d) mixture of diastereomers. Method F; Rt: 0.82 and 0.86 min. m/z: 410.2 (M+NH4)+ Exact mass: 392.1. Compound 145 was separated in it's isomers by preparative SFC (Stationary phase: Chiralpak Diacel AD 30 x 250 mm), Mobile phase: C02, MeOH with 0.4% iPrNH2), the desired fractions were collected, evaporated, dissolved in MeOH and evaporated again yielding compound 145a
(238 mg) and 145b (236 mg) and a mixture of compound 145c and 145d. The mixture of 145c and 145d was further purified by Preparative SFC (Stationary phase: Chiralpak Diacel AD 30 x 250 mm), Mobile phase: C02, EtOH with 0.4% iPrNH2), the desired fractions were collected, evaporated, dissolved in MeOH and evaporated again yielding 145c (29 mg) and 145d (27 mg). 145a and 145b: N-(4-fluoro-3-methyl-phenyl)-3- [[(li?,35)-3-hydroxycyclopentyl]sulfamoyl]benzamide or N-(4-fluoro-3-methyl- phenyl)-3 - [ [( 1 S,3R)-3 -hydroxy cyclopentyl] sulfamoyl]benzamide .
Method F; Rt: 0.85 min. m/z: 410.2 (M+NH4)+ Exact mass: 392.1.
1H NMR (400 MHz, DMSO- g) δ ppm 1.21 (ddd, J=13.3, 7.8, 6.1 Hz, 1 H), 1.36 -
1.64 (m, 4 H), 1.84 - 1.95 (m, 1 H), 2.25 (d, J=l . l Hz, 3 H), 3.37 - 3.47 (m, 1 H), 3.85 - 3.96 (m, 1 H), 4.25-5.00 (1H, br. s), 7.14 (t, J=9.2 Hz, 1 H), 7.35-7.75 (1H, br. s), 7.54 - 7.63 (m, 1 H), 7.68 (dd, J=7.0, 2.2 Hz, 1 H), 7.75 (t, J=7.8 Hz, 1 H), 8.01 (d, J=7.9 Hz, 1 H), 8.19 (d, J=7.7 Hz, 1 H), 8.36 (s, 1 H), 10.46 (br. s., 1 H)
145c and 145d: N-(4-fluoro-3-methyl-phenyl)-3-[[(15',35)-3-hydroxycyclopentyl]- sulfamoyl]benzamide or N-(4-fluoro-3-methyl-phenyl)-3-[[(li?,3i?)-3-hydroxycyclo- pentyl]sulfamoyl]benzamide. Method F; Rt: 0.82 min. m/z: 410.2 (M+NH4) Exact mass: 392.1.
1H NMR (400 MHz, DMSO-d6 ) δ ppm 1.17 - 1.35 (m, 2 H), 1.41 (ddd, J=13.4, 8.0, 5.7 Hz, 1 H), 1.56 (ddd, J=13.2, 7.3, 2.6 Hz, 1 H), 1.69 - 1.83 (m, 2 H), 2.25 (d, J=1.8 Hz, 3 H), 3.59 - 3.72 (m, 1 H), 3.99 - 4.09 (m, 1 H), 4.43 (d, J=3.5 Hz, 1 H), 7.14 (t, J=9.2 Hz, 1 H), 7.55 - 7.63 (m, 1 H), 7.68 (dd, J=7.0, 2.2 Hz, 1 H), 7.73 - 7.84 (m, 2 H), 7.96 - 8.02 (m, 1 H), 8.20 (dt, J=7.9, 1.2 Hz, 1 H), 8.36 (t, J=1.7 Hz, 1 H), 10.48 (br. s., 1 H) 145a: [a] ° : +5.2 ° (c 0.56 w/v %, DMF); 145b: [a] ° : -5.4 ° (c 0.60 w/v %, DMF); 145c: [a] : -3.5 ° (c 0.46 w/v %, DMF); 145d: [a] : +2.5 °(c 0.44 w/v %, DMF)
Compound 146
Figure imgf000088_0001
Synthesis following procedure S2 with 6-oxa-2-azaspiro[3.4]octane oxalate as amine, after completion, the reaction mixture was directly loaded on a silica gel column for purification, using a heptane to EtOAc gradient yielding compound 146. Method F; Rt:
0.93 min. m/z: 422.3 (M+NH4)+ Exact mass: 404.1. 1 H NMR (400 MHz, DMSO-d6) ppm 1.81 (t, J=6.9 Hz, 2 H), 2.26 (d, J=1.8 Hz, 3 H), 3.46 (s, 2 H), 3.57 (t, J=6.9 Hz, 2 H), 3.72 - 3.80 (m, 4 H), 7.15 (t, J=9.1 Hz, 1 H), 7.58 - 7.64 (m, 1 H), 7.69 (dd, J=7.0, 2.2 Hz, 1 H), 7.87 (t, J=7.8 Hz, 1 H), 8.04 (dt, J=8.0, 1.3 Hz, 1 H), 8.32 - 8.41 (m, 2 H), 10.53 (s, 1 H).
Compound 147
Figure imgf000088_0002
Synthesis following procedure S2 with 6-oxa-l-azaspiro[3.3]heptane as amine, after completion, the reaction mixture was directly loaded on a silica gel column for purification, using a heptane to EtOAc gradient yielding compound 147. Method F; Rt:
0.92 min. m/z: 408.2 (M+NH4)+ Exact mass: 390.1. 1H NMR (400 MHz, DMSO-d6 ) δ ppm 2.25 (d, J=1.8 Hz, 3 H), 2.53 (t, J=7.3 Hz, 2 H), 3.73 (t, J=7.4 Hz, 2 H), 4.53 (d, J=7.9 Hz, 2 H), 5.01 (d, J=7.9 Hz, 2 H), 7.15 (t, J=9.1 Hz, 1 H), 7.56 - 7.64 (m, 1 H), 7.68 (dd, J=7.0, 2.2 Hz, 1 H), 7.82 (t, J=7.8 Hz, 1 H), 8.05 - 8.11 (m, 1 H), 8.29 (dt, J=7.8, 1.3 Hz, 1 H), 8.40 (t, J=1.7 Hz, 1 H), 10.51 (s, 1 H) Compound 148
Figure imgf000089_0001
Synthesis following procedure S4 with (5)-(+)-l-cyclohexylethylamine as amine, workup W4. Method F; Rt: 1.23 min. m/z: 436.2 (M+NH4)+ Exact mass: 418.2
Compound 149
Figure imgf000089_0002
Synthesis following procedure S4 with 4,4-difluorocyclohexylamine as amine, workup W4. Method F; Rt: 1.06 min. m/z: 444.5 (M+NH4)+ Exact mass: 426.1.
Compound 150
Figure imgf000089_0003
Synthesis following procedure S4 with 3-buten-2-amine, hydrochloride
as amine, workup W4. Method F; Rt: 1.01 min. m/z: 380.3 (M+NH4)+ Exact mass: 362.1. 1H NMR (400 MHz, DMSO-d6) δ ppm 1.03 (d, J=6.8 Hz, 3 H), 2.25 (d, J=1.8 Hz, 3 H), 3.74 - 3.87 (m, 1 H), 4.87 (dt, J=10.5, 1.4 Hz, 1 H), 5.00 (dt, J=17.3, 1.4 Hz, 1 H), 5.61 (ddd, J=17.3, 10.5, 6.1 Hz, 1 H), 7.14 (t, J=9.2 Hz, 1 H), 7.55 - 7.63 (m, 1 H), 7.68 (dd, J=7.2, 2.3 Hz, 1 H), 7.74 (t, J=7.8 Hz, 1 H), 7.93 (d, J=7.9 Hz, 1 H), 7.96 - 8.01 (m, 1 H), 8.18 (dt, J=7.7, 1.3 Hz, 1 H), 8.35 (t, J=1.7 Hz, 1 H), 10.45 (s, 1 H).
Compound 151
Figure imgf000089_0004
Synthesis following procedure S4 (stirred for 20 hours instead of 3 hours) with (5)-(+)- 2-amino-3-methylbutane as amine, workup W4. Method F; Rt: 1.11 min. m/z: 396.2
(M+NH4)+ Exact mass: 378.1. 1H NMR (400 MHz, CHLOROFORM-d) δ ppm 0.81 (d, J=6.8 Hz, 6 H), 0.95 (d, J=6.8 Hz, 3 H), 1.57 - 1.67 (m, 1 H), 2.28 (d, J=1.8, 3 H), 3.13 - 3.28 (m, 1 H), 4.85 (d, J=8.6 Hz, 1 H), 6.98 (t, J=9.0 Hz, 1 H), 7.36 - 7.46 (m, 1 H), 7.49 - 7.57 (m, 1 H), 7.61 (t, J=7.8 Hz, 1 H), 8.00 (dt, J=7.9, 1.5 Hz, 1 H), 8.12 (dt, J=7.9, 1.5 Hz, 1 H), 8.25 (s, 1 H), 8.39 (t, J=1.9 Hz, 1 H). Compound 152
Figure imgf000090_0001
Synthesis following procedure S4 (stirred for 20 hours instead of 3 hours) with (1R)-1- cyclopropylethylamine as amine, workup W4. 1 H NMR (400 MHz, CHLOROFORM- d) δ ppm -0.05 - 0.05 (m, 1 H), 0.09-0.16 (m, 1 H), 0.20 - 0.36 (m, 1 H), 0.38 - 0.51 (m, 1 H), 0.69-0.81 (m, 1 H), 1.13 (d, J=6.6 Hz, 3 H), 2.27 (d, J=1.8 Hz, 3 H), 2.63 - 2.85 (m, 1 H), 5.10 (d, J=6.8 Hz, 1 H), 6.98 (t, J=8.9 Hz, 1 H), 7.37-7.45 (m, 1 H), 7.52 (dd, J=6.6, 2.4 Hz, 1 H), 7.60 (t, J=7.8 Hz, 1 H), 7.98-8.02 (m, 1 H), 8.08-8.13 (m, 1 H), 8.25 (s, 1 H), 8.38 (t, J=1.7 Hz, 1 H). Method F; Rt: 1.07 min. m/z: 394.2 (M+NH4)+ Exact mass: 376.1.
Compound 174
Figure imgf000090_0002
Synthesis following procedure S4 (stirred for 20 hours instead of 3 hours) with (1R)-1- cyclopropylethylamine as amine, workup W4. The obtained residue was recrystallised from disopropylether/acetonitrile. The precipitate was collected and dried in vacuo at
55°C, resulting in compound 174. 1H NMR (400 MHz, DMSO-d6) δ ppm -0.1 1 - -0.01 (m, 1 H), 0.07 - 0.23 (m, 2 H), 0.29 - 0.38 (m, 1 H), 0.70 - 0.82 (m, 1 H), 0.99 (d, J=6.6 Hz, 3 H), 2.21 - 2.30 (m, 3 H), 2.66 (quin, J=6.8 Hz, 1 H), 7.14 (t, J=9.1 Hz, 1 H), 7.56 - 7.64 (m, 1 H), 7.68 (dd, J=7.0, 2.4 Hz, 1 H), 7.75 (t, J=7.8 Hz, 1 H), 7.85 (br. s., 1 H), 7.93 - 8.07 (m, 1 H), 8.18 (d, J=7.9 Hz, 1 H), 8.37 (t, J=1.7 Hz, 1 H), 10.46 (br. s., 1 H)
Compound 153
Figure imgf000090_0003
Synthesis following procedure S4 (stirred for 20 hours instead of 3 hours) with
3-amino-l-phenylbutane as amine, workup W4. Method F; Rt: 1.19 min. m/z: 458.2 (M+NH4)+ Exact mass: 440.2. 1H NMR (400 MHz, CHLOROFORM-d) δ ppm 1.06 (d, J=6.6 Hz, 3 H), 1.62 - 1.76 (m, 2 H), 2.25 (d, J=l .8 Hz, 3 H), 2.44 - 2.64 (m, 2 H), 3.30 - 3.43 (m, 1 H), 5.05 (d, J=8.4 Hz, 1 H), 6.96 (t, J=8.9 Hz, 1 H), 7.00-7.04 (m, 2 H), 7.09 - 7.17 (m, 1 H), 7.17 - 7.25 (m, 2 H), 7.36-7.42 (m, 1 H), 7.50 (dd, J=6.8, 2.4 Hz, 1 H), 7.57 (t, J=7.8 Hz, 1 H), 7.95 (m, J=7.8, 1 H), 8.10 (m, J=7.8 Hz, 1 H), 8.25 (s, 1 H), 8.37 (t, J=1.5 Hz, 1 H)
Compound 154
Figure imgf000091_0001
3-[(4-fluoro-3-methyl-phenyl)carbamoyl]benzenesulfonyl chloride (500 mg,
1.53 mmol) and DIPEA (657 μί, 3.8 mmol, 2.5 eq) dissolved in CH2CI2 (15 mL) were added to a tube containing 3-amino-l-Boc-3-methyl-azetidine (1.1 eq). The reaction mixture was stirred for 20 hours. 1M HC1 (5 mL) was added and the mixture was stirred for 5 minutes. The organic layer was separated and loaded on a silica gel column. The mixture was purified using gradient elution from heptane to EtOAc, resulting in compound 154 (721 mg). Method F; Rt: 1.11 min. m/z: 478.2 (M+H)+ Exact mass: 477.2.
Compound 155
Figure imgf000091_0002
Prepared as described for compound 154 using l-Boc-3-aminopiperidine instead of 3-amino-l-Boc-3-methyl-azetidine. Method F; Rt: 1.13 min. m/z: 492.1 (M+H)+ Exact mass: 491.2.
Compound 156
Figure imgf000091_0003
Prepared as described for compound 154 using (+/-)-3-amino-l-N-Boc-pyrrolidine instead of 3-amino-l-Boc-3-methyl-azetidine. Method F; Rt: 1.08 min. m/z: 478.2 (M+H)+ Exact mass: 477.2 1H NMR (400 MHz, CHLOROFORM- ) δ ppm 1.36 (s, 9 H), 1.71 - 1.92 (m, 1 H), 1.92 - 2.15 (m, 1 H), 2.28 (d, J=1.8 Hz, 3 H), 3.10-3.24 (m, 1 H), 3.24-3.44 (m, 3 H), 3.81 - 3.94 (m, 1 H), 5.50 - 6.00 (m, 1 H), 6.98 (t, J=9.0 Hz, 1 H), 7.40 - 7.48 (m, 1 H), 7.52 - 7.71 (m, 2 H), 7.93-8.03 (m, 1 H), 8.04 - 8.17 (m, 1 H), 8.31 (br. s., 1 H), 8.45 - 8.88 (m, 1 H). Compound 157
Figure imgf000092_0001
Compound 154 (721 mg, 1.51 mmol) was dissolved in CH2C12 (10 mL) and HC1 (6M in iPrOH, 2.5 mL) was added. The mixture was stirred overnight and the volatiles were removed in vacuo, resulting in N-(4-fluoro-3-methyl-phenyl)-3-[(3-methylazetidin- 3-yl)sulfamoyl]benzamide hydrochloride as a white solid (0.57 g). To N-(4-fluoro-3- methyl-phenyl)-3 - [(3 -methylazetidin-3 -yl)sulfamoyl]benzamide hydrochloride (150 mg) in CH2C12 (10 mL), DIPEA (263 μ∑, 1.5 mmol) and methyl chloroformate (44 μί, 0.57 mmol) were added. The mixture was concentrated under a gentle flow of nitrogen at 55°C until only 2 mL remained. This residue was purified using silica gel column chromatography (gradient elution: EtO Ac-heptane 0: 100 to 100:0). The desired fractions were concentrated under reduced pressure and the obtained product was dried in a vacuum oven at 55°C yielding compound 157 (74.2 mg) as a bright white powder. Method F; Rt: 0.93 min. m/z: 436.1 (M+H)+ Exact mass: 435.1. 1H NMR (400 MHz,
DMSO-dg) δ ppm 1.36 (s, 3 H), 2.25 (d, J=1.5 Hz, 3 H), 3.52 (s, 3 H), 3.56-3.68 (m, 2 H), 3.83-3.93 (m, 2 H), 7.14 (t, J = 9.2 Hz, 1 H), 7.57 - 7.62 (m, 1 H), 7.68 (dd, J=6.8, 2.4 Hz, 1 H), 7.77 (t, J=7.9 Hz, 1 H), 8.01 (m, J=7.9 Hz, 1 H), 8.21 (m, J=7.9 Hz, 1 H), 8.37 (t, J=1.5 Hz, 1 H), 8.48 (bs, 1 H), 10.49 (s, 1 H)
Compound 158
Figure imgf000092_0002
Prepared similarly as described for compound 157, starting from compound 156 instead of compound 154, via intermediate N-(4-fluoro-3-methyl-phenyl)-3-(pyrrolidin-3-yl- sulfamoyl)benzamide hydrochloride. Method F; Rt: 0.91 min. m/z: 436.2 (M+H)+ Exact mass: 435.1. 1H NMR (400 MHz, DMSO-de) δ ppm 1.61-1.77 (m, 1 H), 1.80- 1.98 (m 1 H), 2.25 (d, J=1.5 Hz, 3 H), 3.00-3.12 (m, 1 H), 3.14 - 3.27 (m, 1 H), 3.26 - 3.39 (m, 2 H), 3.50-3.58 (m, 3 H), 3.67 - 3.76 (m, 1 H), 7.14 (t, J=9.2 Hz, 1 H), 7.57 - 7.63 (m, 1 H), 7.68 (dd, J=7.2, 2.3 Hz, 1 H), 7.78 (t, J=7.8 Hz, 1 H), 7.97 - 8.04 (m, 1 H), 8.04 - 8.18 (m, 1 H), 8.18 - 8.25 (m, 1 H), 8.37 (t, J=1.5 Hz, 1 H), 10.48 (s, 1 H) Compound 159
Figure imgf000093_0001
Prepared similarly as described for compound 157, starting from compound 155 instead of compound 154, via intermediate N-(4-fluoro-3-methyl-phenyl)-3-(3-piperidyl- sulfamoyl)benzamide hydrochloride. Method F; Rt: 0.96 min. m/z: 467.1 (M+NH4)+ Exact mass: 449.1. The racemic compound 159 was separated by Preparative SFC
(Stationary phase: Chiralpak Daicel IC 20 x 250 mm), Mobile phase: C02, MeOH with 0.2% iPrNH2), the desired fractions were collected, evaporated, dissolved in methanol and evaporated again, resulting in enantiomer 159a and 159b.
Columns: ID-H (Daicel) 250 mm x 4.6 mm; Flow: 3 mL/min; Mobile phase: 20% EtOH (containing 0.2% iPrNH2) hold 15.00 min; Temperature: 30°C ; Rt: 9.6 min
(159a), Rt: 11.0 min (159b)
Compound 160
Figure imgf000093_0002
Method B; Rt: 4 min. m/z: 443.1 (M+H) Exact mass: 442.0
1H NMR (400 MHz, DMSO-de) δ ppm 1.41 (s, 3 H) 4.14 (d, J= 6.3 Hz, 2 H) 4.56 (d, J=6.0 Hz, 2 H) 7.42 (t, J=8.8 Hz, 1 H) 7.74 - 7.82 (m, 2 H) 8.04 (s, 1 H) 8.15 - 8.24 (m, 2 H) 8.37 (t, J=1.5 Hz, 1 H) 8.54 (br. s, 1 H) 10.67 (br. s, 1 H).
Compound 161
Figure imgf000093_0003
l-pyridin-4-yl-ethylamine (220 mg, 1.8 mmol) and 3-[(4-fluoro-3-methyl-phenyl)- carbamoyl]benzenesulfonyl chloride (500 mg, 1.53 mmol) were dissolved in CH2C12 (10 mL). DIPEA (6.2 mmol) was added at 0°C and the mixture was stirred at 25°C for 4 hours. The mixture was washed with water (20 mL) and the aqueous layer was extracted with CH2C12 (3 x 20 mL). The combined organic layers were washed with brine and dried over Na2S04. The solvent was removed in vacuo and the obtained residue was purified by reversed phase high performance liquid chromatography (mobile phase: CH3CN in water (0.1% TFA) from 30% to 60%). The pure fractions were collected and neutralized with solid NaHC03. The organic solvent was removed in vacuo and the formed precipitate was filtered, washed with H20 (5 mL) and dried under high vacuum. The obtained residue was suspended in water (5 mL) and the aqueous layer was lyophilized to dryness, resulting in compound 161 (410 mg). Method A; Rt: 4.34 min. m/z: 414.3 (M+H)+ Exact mass: 413.1. 1H NMR (400 MHz, DMSO-d6) δ ppm 1.23 (d, J=7.0 Hz, 3 H) 2.26 (d, J=1.5 Hz, 3 H) 4.34 - 4.50 (m, 1 H) 7.15 (t, J=9.3 Hz, 1 H) 7.20 - 7.24 (m, 2 H) 7.56 - 7.66 (m, 2 H) 7.68 (dd, J=7.0, 2.3 Hz, 1 H) 7.86 (m, J=7.8 Hz, 1 H) 8.13 (m, J=7.8 Hz, 1 H) 8.26 (t, J=1.3 Hz, 1 H) 8.32 - 8.39 (m, 2 H) 8.55 (d, J=8.3 Hz, 1 H) 10.41 (s, 1 H).
Compound 162
Figure imgf000094_0001
Prepared similarly as described for compound 161, using l-(3-pyridyl)ethanamine instead of l-pyridin-4-yl-ethylamine. Method D; Rt: 5.16 min. m/z: 414.3 (M+H)+ Exact mass: 413.1.
Compound 163
Figure imgf000094_0002
Prepared similarly as described for compound 161, using l-(2-pyridyl)ethanamine instead of l-pyridin-4-yl-ethylamine. Method A; Rt: 4.60 min. m z: 414.3 (M+H)+ Exact mass: 413.1.
Compound 164
Figure imgf000094_0003
Prepared similarly as described for compound 161, using l-(l-methyl-4- piperidyl)ethanamine instead of l-pyridin-4-yl-ethylamine. Method B; Rt: 3.35 min. m/z: 434.4 (M+H)+ Exact mass: 433.2.
Compound 165
Figure imgf000094_0004
Prepared similarly as described for compound 161, using 4-morpholinobutan-2-amine instead of l-pyridin-4-yl-ethylamine. Method B; Rt: 3.33 min. m/z: 450.3 (M+H)+ Exact mass: 449.2.
Compound 166
Figure imgf000095_0001
Prepared similarly as described for compound 161, using (i?)-l-phenylethanamine instead of l-pyridin-4-yl-ethylamine. The impure compound was purified by preparative high-performance liquid chromatography (column: Luna 150*30mm*5u, mobile phase: CH3CN in water (0.1% NH4HC03) from 40% to 70%, flow rate: 35 ml/min). Method B; Rt: 4.45 min. m/z: 413.3 (M+H)+ Exact mass: 412.1. [«]D : + 55° (c 0.12 w/v, methano 1) .
Compound 167
Figure imgf000095_0002
Prepared similarly as described for compound 166, using (5)-l-phenylethanamine instead of (i?)-l-phenylethanamine. Method B; Rt: 4.45 min. m/z: 413.3 (M+H) Exact mass: 412.1. [α]η° : - 57° (c 0.12 w/v, methanol).
Compound 168
Figure imgf000095_0003
Synthesis following procedure S4 (20 hours reaction time instead of 3 hours) with 2-aminoindane as amine, workup W4. The obtained residue was recrystallised from Diisopropylether/acetonitrile, resulting in compound 168. Method F; Rt: 1.14 min. m/z:
442.2 (M+NH4)+ Exact mass: 424.1. 1H NMR (400 MHz, DMSO-d6) δ ppm 2.25 (d, J=1.8 Hz, 3 H), 2.72 (dd, J=15.6, 7.0 Hz, 2 H), 2.96 (dd, J=15.8, 7.5 Hz, 2 H), 3.95 (quin, J=7.3 Hz, 1 H), 7.08 - 7.17 (m, 5 H), 7.57 - 7.63 (m, 1 H), 7.68 (dd, J=6.9, 2.3 Hz, 1 H), 7.79 (t, J=7.8 Hz, 1 H), 8.03 - 8.12 (m, 1 H), 8.13 - 8.28 (m, 2 H), 8.41 (t, J=1.7 Hz, 1 H), 10.49 (br. s., 1 H) Compound 169
Figure imgf000096_0001
Prepared similarly as described for compound 166, using 1 -phenylpropan-2-amine instead of (R)-l-phenylethanamine. Method B; Rt: 4.60 min. m/z: 427.3 (M+H)+ Exact mass: 426.1.
Figure imgf000096_0002
Ri Synthetic/ [M+NH
LC-MS Rt -.+ Exact
# Amine used work up ] or
method (min.) mass Procedure [M+H]+
H
4-Amino- 1 -
179 methyl- S4*/W4 F 0.81 406.1 405.1
I pyrrolidin-2-one
5 -Amino- 1-
180 methyl- S4*/W4 F 0.81 420.2 419.1
I piperidin-2-one
H
3 -Amino- 1-
181 methylpyrrolidi S4/W4 F 0.84 423.1 405.1
I n-2-one
3-Amino-l-N-
182 S4*/W4 F 1.06 481.2 463.2 boc-azetidine l-(trifluoro-
183 methyl)cyclo- S4*/W4 F 1.03 434.1 416.1
Figure imgf000097_0001
propanamine
S4*: reaction time 20 hours instead of 3 hours
Compound 175. 1H NMR (400 MHz, DMSO-dg) δ ppm 2.25 (d, J=1.5 Hz, 3 H), 2.62 (dd, J=15.7, 6.5 Hz, 1 H), 3.07 (dd, J=15.7, 6.7 Hz, 1 H), 4.11 (quin, J=6.2 Hz, 1 H), 4.50 (dd, J=7.9, 6.2 Hz, 1 H), 5.14 (d, J=5.7 Hz, 1 H), 6.92 (d, J=7.5 Hz, 1 H), 7.06 -
7.24 (m, 4 H), 7.55 - 7.65 (m, 1 H), 7.69 (dd, J=7.0, 2.4 Hz, 1 H), 7.77 (t, J=7.8 Hz, 1 H), 8.05 - 8.15 (m, 1 H), 8.19 - 8.26 (m, 1 H), 8.31 (d, J=8.4 Hz, 1 H), 8.47 (t, J=1.7 Hz, 1 H), 10.45 (s, 1 H)
Compound 178. 1H NMR (400 MHz, DMSO-dg) δ ppm 1.51 - 1.72 (m, 1 H), 1.86 - 1.99 (m, 1 H), 2.22 - 2.31 (m, 3 H), 2.60-2.74 (m, 1 H), 2.74 - 2.85 (m, 1 H), 3.26 -
3.41 (m, 1 H), 4.38 (t, J=6.2 Hz, 1 H), 5.32 - 5.39 (m, 1 H), 6.96 - 7.09 (m, 1 H), 7.11 - 7.21 (m, 3 H), 7.28 - 7.37 (m, 1 H), 7.51 - 7.65 (m, 1 H), 7.69 (dd, J=7.0, 2.4 Hz, 1 H), 7.72 - 7.82 (m, 2 H), 8.05 - 8.12 (m, 1 H), 8.17 - 8.24 (m, 1 H), 8.43 (t, J=1.7 Hz, 1 H), 10.48 (s, 1 H)
Compound 179. 1H NMR (400 MHz, DMSO-dg) δ ppm 1.99 (dd, J=5.1, 16.7 Hz, 1 H),
2.25 (d, J=1.8 Hz, 3 H), 2.35 (dd, J=8.4, 16.7 Hz, 1 H), 2.66 (s, 3 H), 3.10 (dd, J=10.1, 4.6 Hz, 1 H), 3.47 (dd, J=10.3, 7.3 Hz, 1 H), 3.80 - 3.92 (m, 1 H), 7.14 (t, J=9.2 Hz, 1 H), 7.53 - 7.63 (m, 1 H), 7.68 (dd, J=7.0, 2.2 Hz, 1 H), 7.74 - 7.86 (m, 1 H), 7.97 - 8.08 (m, 1 H), 8.15 - 8.32 (m, 2 H), 8.37 (s, 1 H), 10.48 (s, 1 H). Racemic compound 179 was separated in enantiomers 179a and 179b by Preparative SFC (Stationary phase: Chiralpak Diacel AD 30 x 250 mm), Mobile phase: C02, iPrOH with 0.4% iPrNH2) The collected fractions were concentrated in vacuo resulting in compound 179a and 179b. Columns: AD-H (diacel) 250 mm x 4.6 mm; Flow: 5 mL/min; Mobile phase: 30% iPrOH (containing 0.2% iPrNH2) hold 4.00 min, up to 50% in 1 min and hold 2.00 min @ 50%; Temperature: 40°C Rt: 2.2 min (179a); 2.9 min (179b). 179a: +6.1 ° (589 nm, c 0.6225 w/v %, MeOH, 20 °C). 179b: -6.1 ° (589 nm, c 0.506 w/v %, MeOH, 20°C).
Compound 180. 1H NMR (400 MHz, DMSO-d6) δ ppm 1.55 - 1.79 (m, 2 H), 2.01 - 2.36 (m, 5 H), 2.68 (s, 3 H), 3.06 (dd, J=12.3, 6.8 Hz, 1 H), 3.25 - 3.30 (m, 1 H), 3.46 - 3.58 (m, 1 H), 7.14 (t, J=9.1 Hz, 1 H), 7.52 - 7.63 (m, 1 H), 7.64 - 7.71 (m, 1 H), 7.78 (t, J=7.8 Hz, 1 H), 8.01 - 8.09 (m, 1 H), 8.11 - 8.27 (m, 2 H), 8.39 (t, J=1.7 Hz, 1 H), 10.47 (s, 1 H)
Compound 181. 1H NMR (400 MHz, DMSO-d6) δ ppm 1.59 (dq, J=12.4, 9.3 Hz, 1 H), 1.93 - 2.16 (m, 1 H), 2.25 (d, J=1.5 Hz, 3 H), 2.69 (s, 3 H), 3.06 - 3.24 (m, 2 H), 4.00 (t, J=9.1 Hz, 1 H), 7.14 (t, J=9.2 Hz, 1 H), 7.54 - 7.64 (m, 1 H), 7.65 - 7.71 (m, 1 H), 7.74 (t, J=7.8 Hz, 1 H), 7.99 - 8.09 (m, 1 H), 8.25 (br. s, 1 H), 8.11 - 8.20 (m, 1 H), 8.44 (t, J=1.7 Hz, 1 H), 10.42 (s, 1 H).
Compound 182. 1H NMR (400 MHz, DMSO-d6) δ ppm 1.12 - 1.52 (m, 9 H), 2.26 (d, J=1.3 Hz, 3 H), 3.40-3.60 (m 2 H), 3.80-4.00 (m, 2 H), 4.02 - 4.19 (m, 1 H), 7.15 (t, J=9.2 Hz, 1 H), 7.57 - 7.66 (m, 1 H), 7.70 (dd, J=7.0, 2.2 Hz, 1 H), 7.80 (t, J=7.8 Hz, 1 H), 8.01 (m, J=8.1 Hz, 1 H), 8.26 (m, J=7.9 Hz, 1 H), 8.38 (t, J=1.0 Hz, 1 H), 8.51 (d, J=8.4 Hz, 1 H), 10.50 (s, 1 H).
Compound 183. 1H NMR (400 MHz, CHLOROFORM-d) δ ppm 1.19 - 1.43 (m, 4 H), 2.28 (d, J=1.8 Hz, 3 H), 5.74 (br. s., 1 H), 6.99 (t, J=8.8 Hz, 1 H), 7.37 (m, J=8.4, 3.7 Hz, 1 H), 7.45 - 7.54 (m, 1 H), 7.64 (t, J=7.8 Hz, 1 H), 7.88 (br. s., 1 H), 8.03 (m, J=8.1 Hz, 1 H), 8.10 (m, J=7.9 Hz, 1 H), 8.29 - 8.38 (m, 1 H)
Figure imgf000098_0001
Synthesis following procedure S4 with 3-aminocyclobutanol
as amine, 1 hour reaction time instead of 3 hour, workup W4. Method F; Rt: 0.81 min. m/z: 396.2 (M+NH4)+ Exact mass: 378.1. SFC: Columns: Diacel AD-H (250 mm x 4.6 mm); Flow: 5 mL/min Mobile phase: 30% MeOH (containing 0.2% iPrNH2) hold 4.00 min, up to 50% in 1 min and hold 2.00 min at 50%; Temperature: 40°C; Rt: 184a (2.5 min), 184b (3.4 min). The diastereomeric mixture of compound 184 was separated in diastereoisomers (Prep SFC (Stationary phase: Chiralpak Diacel AD 30 x 250 mm), Mobile phase: C02, MeOH with 0.4% iPrNH2). The obtained fractions were concentrated under reduced pressure and dried in vacuo at 55°C, resulting in compound 184a and 184b.
Compound 184a
Figure imgf000099_0001
1H NMR (600 MHz, DMSO-de) δ ppm 1.84 - 1.91 (m, 2 H), 1.92 - 1.98 (m, 2 H), 2.25 (d, J=1.8 Hz, 3 H), 3.77 (quin, J=6.9 Hz, 1 H), 4.10 - 4.14 (m, 1 H), 4.93 (d, J=4.9 Hz, 1 H), 7.14 (t, J=9.2 Hz, 1 H), 7.59 (ddd, J=8.8, 4.6, 2.7 Hz, 1 H), 7.68 (dd, J=7.1, 2.7 Hz, 1 H), 7.76 (t, J=7.8 Hz, 1 H), 7.96 (ddd, J=7.8, 1.9, 1.1 Hz, 1 H), 8.06 (br. s., 1 H), 8.20 (dt, J=7.8, 1.5 Hz, 1 H), 8.33 (t, J=1.8 Hz, 1 H), 10.49 (br. s., 1 H).
Compound 184b
Figure imgf000099_0002
1H NMR (600 MHz, DMSO-de) δ ppm 1.54 - 1.60 (m, 2 H), 2.19 - 2.24 (m, 2 H), 2.25 (d, J=1.8 Hz, 3 H), 3.09 - 3.19 (m, 1 H), 3.62 - 3.68 (m, 1 H), 5.00 (d, J=5.6 Hz, 1 H), 7.14 (t, J=9.2 Hz, 1 H), 7.59 (ddd, J=8.5, 4.5, 2.8 Hz, 1 H), 7.68 (dd, J=7.0, 2.2 Hz, 1 H), 7.75 (t, J=7.8 Hz, 1 H), 7.97 (ddd, J=7.8, 1.9, 1.0 Hz, 1 H), 8.02 (br. s., 1 H), 8.19 (ddd, J=7.8, 1.8, 1.1 Hz, 1 H), 8.34 (t, J=1.6 Hz, 1 H), 10.48 (s, 1 H)
Compound 185
Figure imgf000099_0003
Prepared similarly as described for compound 157, starting from compound 182 instead of compound 154, via intermediate 3-(azetidin-3-ylsulfamoyl)-N-(4-fluoro-3-methyl- phenyl)benzamide hydrochloride. Method F; Rt: 0.89 min. m/z: 439.2 (M+NH4)+ Exact mass: 421.1.1H NMR (400 MHz, DMSO-d6) δ ppm 2.25 (d, J=1.8 Hz, 3 H), 3.45-3.60 (m, 5 H), 3.85-4.05 (m, 2 H), 4.07 - 4.17 (m, 1 H), 7.15 (t, J=9.1 Hz, 1 H), 7.53 - 7.64 (m, 1 H), 7.65 - 7.71 (m, 1 H), 7.78 (t, J=7.8 Hz, 1 H), 7.94 - 8.03 (m, 1 H), 8.23 (m, J=7.9 Hz, 1 H), 8.33 (t, J=1.7 Hz, 1 H), 8.44 - 8.63 (br. s, 1 H), 10.49 (s, 1 H). Compound 186
Figure imgf000100_0001
3-(isopropylsulfamoyl)benzoic acid (250 mg, 1.03 mmol), 4-fluoro-3,5-dimethyl- aniline (157 mg, 1.13 mmol) and DIPEA (398 mg, 3.08 mmol) were mixed in acetonitrile (10 mL) at room temperature under a nitrogen atmosphere. HATU (430 mg, 1.13 mmol) was added and the mixture was stirred overnight. EtOAc (100 mL) was added and the mixture was washed with 1M HC1, sat NaHC03 and brine. After drying over MgS04 and evaporation to dryness in vacuo, the obtained residue was crystallized from MeOH (10 mL) to provide a white solid (216 mg). Method F; Rt: 1.04 min. m/z: 382.2 (M+NH4)+ Exact mass: 364.1. 1 H NMR (400 MHz, DMSO-d6) δ ppm 0.96 (d, J=6.6 Hz, 6 H), 2.23 (d, J=2.0 Hz, 6 H), 3.23 - 3.29 (m, 1 H), 7.48 (d, J=6.6 Hz, 2 H), 7.66 - 7.80 (m, 2 H), 7.95 - 8.04 (m, 1 H), 8.18 (d, J=7.9 Hz, 1 H), 8.35 (t, J=1.7 Hz, 1 H), 10.37 (s, 1 H).
Compound 187
Figure imgf000100_0002
A solution of 2-fluoro-6-methylbenzoic acid (10 g, 0.0649 mol) in HO Ac (300 mL) was stirred on a water-bath containing a bit of ice. At ~ 15°C, HN03 (65%, 32.7 mL) was added dropwise. After addition, H20 (30 mL) was added slowly. After addition, Br2 (3.7 mL) was added dropwise. A solution of silver nitrate (14.33 g, 0.0844 mol) in H20 (100 mL) was added dropwise over a period of 30 minutes. After addition, the reaction mixture was stirred at room temperature for 3 hours 30 minutes. The reaction mixture was poured into H20 (850 mL), and EtOAc (300 mL) was added. The mixture was stirred vigorously for 5 minutes. Both upper liquid layers were decanted from a residue. The separated water layer was combined with the residue, and extracted with EtOAc. Both upper liquid layers were decanted from the residue. The separated water layer was combined with the residue, and extracted again with EtOAc. The organic layers were combined, washed with satured NaCl and dried with Na2S04, filtered off, evaporated, and co-evaporated with toluene. The obtained solid residue was stirred in a small amount of diisopropylether, filtered off, washed with diisopropylether, resulting in 3-bromo-6-fluoro-2-methyl-benzoic acid (4 g).The filtrate was evaporated. The residue was stirred in heptane, filtered off, washed with heptanes (3x), and dried at 50°C in vacuo, resulting in a mixture of bromo-6-fluoro-2-methyl-benzoic acid and 2- fluoro-6-methylbenzoic acid (12 g, 1/0.4 ratio). 3-bromo-6-fluoro-2-methyl-benzoic acid (4 g, 0.0172 mol) was added portionwise to stirring chlorosulfonic acid (25 mL). The resulting solution was stirred at 115°C for 2 hours, left standing at room
temperature overnight and next stirred at 115°C for 3 hours more. The reaction mixture was allowed to reach room temperature, and added dropwise to a stirring mixture of crushed ice (150 g) and H20 (50 mL). The product was extracted with EtOAc (2 x). The combined organic layers were washed with brine, dried with Na2S04, filtered off, and evaporated, resulting in a crude mixture containing 5-bromo-3-chlorosulfonyl-2- fluoro-6-methyl-benzoic acid (4.4 g) (Na2C03, 1.407 g, 0.0133 mol) was dissolved in water (25 mL). A solution of (S)-3-aminotetrahydrofuran (2.312 g, 0.0265 mol) in THF (20 mL) was added, and the reaction mixture was cooled to 0°C on an ice-bath. A solution of crude 5-bromo-3-chlorosulfonyl-2-fluoro-6-methyl-benzoic acid (4.4 g) in THF (30 mL) was added dropwise at 0°C. After addition, the reaction mixture was stirred at 0°C for 1 hour, and at room temperature for 2 hours. The mixture was concentrated till ~ 35 mL remained, then left standing for 70 hours. The solid was filtered off and washed with H20 (2x). The filtrate was washed with Et20. The separated waterlayer was acidified with IN HC1 (30 mL), and the product was extracted with 2-MeTHF. The separated waterlayer was acidified further till pH ~ 2 and extracted with 2-MeTHF. The organic layer was washed with brine, dried with Na2S04 and filtered, resulting in crude 5-bromo-2-fluoro-6-methyl-3-[[(3S)-tetrahydrofuran-3- yl]sulfamoyl]benzoic acid (6.5 g). To a stirring solution of crude 5-bromo-2-fluoro-6- methyl-3-[[(3S)-tetrahydrofuran-3-yl]sulfamoyl]benzoic acid (1.3 g) in CH3CN (30 mL ) under N2-atm triethylamine (1.42 mL, 0.0102 mol ), 3,4-difluoroaniline (0.446 mL, 4.42 mmol ) and HATU (1.55 g, 4.08 mmol ) were successively added. The reaction mixture was stirred at room temperature for 16 hours. The volatiles were evaporated and the obtained residue was purified by silica gel chromatography (heptane-EtOAc 100/0 to 0/100 ], resulting in compound 187 (0.45 g).An impure fraction was further purified by Preparative HPLC (Stationary phase: RP XBridge Prep CI 8 OBD- 10μιη,30χ150ιηιη), Mobile phase: 0.25% NH4HC03 solution in water, CH3CN), resulting in more compound 187 (0.048 g)
Method F; Rt: 1.06 min. m/z: 491.0 (M-H)~ Exact mass:492.0. 1H NMR (400 MHz, DMSO-dg) δ ppm 1.66 - 1.76 (m, 1 H), 1.94 - 2.05 (m, 1 H), 2.41 (s, 3 H), 3.43 (dd, J=8.9, 4.5 Hz, 1 H), 3.58 - 3.65 (m, 1 H), 3.68 (dd, J=8.9, 6.3 Hz, 1 H), 3.71 - 3.78 (m, 1 H), 3.83 - 3.92 (m, 1 H), 7.36 - 7.42 (m, 1 H), 7.43 - 7.52 (m, 1 H), 7.85 (ddd, J=12.8, 7.5, 2.4 Hz, 1 H), 8.02 (d, J=6.8 Hz, 1 H), 8.55 (s, 1 H), 11.09 (s, 1 H) Compound 188
Figure imgf000102_0001
Compound 187 (0.45 g, 0.912 mmol ) was dissolved in MeOH (20 mL) and THF (30 mL). To the resulting solution, triethylamine (0.254 mL, 1.82 mmol) was added and the mixture was stirred with 10% Pd/C (0.2 g) under hydrogen atmosphere at room temperature. After 3 hours, the catalyst was filtered off over dicalite, and washed with MeOH (3x) and THF (lx). The volatiles were removed in vacuo and the obtained residue was dissolved in hot MeOH (10 mL) and hot H20 (10 mL) was added. The volume was concentrated till ~ 15 mL, and left standing for 1 hour. The precipitated product was filtered off, washed with H20 (3x), and dried at 50°C in vacuo, resulting in compound 188 (245 mg). Method F; Rt: 0.93 min. m/z: 413.2 (M-H)~ Exact mass: 414.1.19 F NMR (377 MHz, DMSO-d6) 5 ppm -143.7 - -143.2 (m, 1 F), -137.1 - -136.5 (m, 1 F), -114.8 (d, J=7.9 Hz, 1 F). 1 H NMR (400 MHz, DMSO-d6) δ ppm 1.66 - 1.77 (m, 1 H), 1.91 - 2.03 (m, 1 H), 2.39 (s, 3 H), 3.43 (dd, J=9.0, 4.6 Hz, 1 H), 3.57 - 3.70 (m, 2 H), 3.70 - 3.77, (m, 1 H), 3.78 - 3.86 (m, 1 H), 7.35 (d, J=8.1 Hz, 1 H), 7.39 - 7.52 (m, 2 H), 7.79 (t, J=7.8 Hz, 1 H), 7.87 (ddd, J=12.9, 7.5, 2.1 Hz, 1 H), 8.32 (br. s., 1 H), 11.00 (s, 1 H).
Compound 189
Figure imgf000102_0002
Compound 189 was prepared similarly as described for compound 188, using 4-f uoro- 3-methylaniline instead of 3,4-difluoroaniline. Method F; Rt: 0.94 min. m/z: 409.2 (M- H)~ Exact mass:410.1. 19F NMR (377 MHz, DMSO-d6) δ ppm -122.40 (dtd, J=9.3, 4.6, 4.6, 2.1 Hz, 1 F), -114.96 (d, J=7.2 Hz, 1 F). 1H NMR (400 MHz, DMSO- 6) δ ppm 1.67 - 1.77 (m, 1 H), 1.92 - 2.03 (m, 1 H), 2.24 (d, J=1.5 Hz, 3 H), 2.38 (s, 3 H), 3.43 (dd, J=8.8, 4.6 Hz, 1 H), 3.58 - 3.64 (m, 1 H), 3.65 - 3.70 (m, 1 H), 3.70 - 3.77 (m, 1 H), 3.78 - 3.86 (m, 1 H), 7.14 (dd, J=9.1 Hz, 1 H), 7.34 (d, J=8.1 Hz, 1 H), 7.45 - 7.53 (m, 1 H), 7.63 (dd, J=7.0, 2.4 Hz, 1 H), 7.77 (dd, J=7.9 Hz, 1 H), 8.30 (br. s., 1 H), 10.72 (s, 1 H). Differential scanning calorimetry From 30 to 300 °C at 10°C/min: Peak at 157.0 °C
Compound 190
Figure imgf000103_0001
Na2C03 (1.60 g, 0.0151 mol) was dissolved in water (25 mL). A solution of 3- methyloxetan-3-amine (2.63 g, 0.0302 mol) in THF (20 mL) was added, and the reaction mixture was cooled to 0°C on an ice-bath. A solution of crude 5-bromo-3- chlorosulfonyl-2-fluoro-6-methyl-benzoic acid (5 g) in THF (30 mL) was added dropwise at 0°C. After addition, the reaction mixture was stirred vigorously at 0°C for 30 minutes, and at room temperature for 2 hours. The organic volatiles were evaporated, and the remaining ~ 30 mL was washed with Et20 (50 mL). The separated waterlayer was acidified with IN HC1 (40 mL), and the product was extracted with 2- MeTHF (2x). The combined organic layers were washed with brine, dried with Na2SC"4, filtered off, evaporated, and co-evaporated with CH3CN, resulting in crude 5-bromo-2-fluoro-6-methyl-3-[(3-methyloxetan-3-yl)sulfamoyl]benzoic acid (3.6 g) To a solution of crude 5-bromo-2-fluoro-6-methyl-3-[(3-methyloxetan-3- yl)sulfamoyl]benzoic acid (0.72 g, 0.00188 mol ) in CH3CN (15 mL ) under N2-atm was successively added NEt3 (0.786 mL, 0.00565 mol ), 4-fluoro-3-methylaniline (0.313 g, 0.00245 mol), and HATU (0.86 g, 0.00226 mol ). The reaction mixture was stirred at room temperature for 20 hours. More 4-fluoro-3-methylaniline (0.1 g) and HATU (0.3 g) were added, and the reaction was continued for 20 hours. The volatiles were evaporated. The residue was purified by silica gel Chromatography (heptane- EtOAc 100/0 to 0/100). The desired fractions were combined and evaporated. The residue was stirred in diisopropylether, filtered off, washed with diisopropylether (3x), and dried at 50°C, resulting in compound 190 (0.38 g). m/z: 486.9 (M-H)~ Exact mass:488.0. 19F NMR (377 MHz, DMSO-d6) δ ppm -122.15 - -121.89 (m, 1 F), -116.05 (d, J=6.4 Hz, 1 F). 1H NMR (400 MHz, DMSO-d6) δ ppm 1.47 (s, 3 H), 2.25 (d, J=1.5 Hz, 3 H), 2.40 (s, 3 H), 4.22 (d, J=6.6 Hz, 2 H), 4.62 (d, J=6.4 Hz, 2 H), 7.16 (dd, J=9.2 Hz, 1 H), 7.44 - 7.51 (m, 1 H), 7.61 (dd, J=6.9, 2.3 Hz, 1 H), 8.01 (d, J=6.8 Hz, 1 H), 8.86 (br. s., 1 H), 10.81 (s, 1 H)
Synthesis of 2-fluoro-6-methyl-3-[(3-methyloxetan-3-yl)sulfamoyl]benzoic acid A solution of 5-bromo-2-fluoro-6-methyl-3-[(3-methyloxetan-3-yl)sulfamoyl]benzoic acid (0.9 g) and triethylamine (0.98 mL, 7.1 mmol) in MeOH (30 mL) was stirred with Pd/C 10% (0.1 g) at room temperature under a hydrogen atmosphere. After the calculated amount of hydrogen was taken up, the catalyst was filtered off. The filtrate was concentrated in vacuo, and co-evaporated with CH3CN. The obtained residue containing 2-fluoro-6-methyl-3-[(3-methyloxetan-3-yl)sulfamoyl]benzoic acid was used as such. Method F; Rt: 0.38 min. m/z: 302.0 (M-H)~ Exact mass:303.1
Compound 191
Figure imgf000104_0001
Triethylamine (0.206 mL, 0.00149 mol ) was added to a stirring mixture of 2-fluoro-6- methyl-3-[(3-methyloxetan-3-yl)sulfamoyl]benzoic acid (0.15 g, 0.000495 mol ) and CH3CN (10 mL ) under N2-atm. To the resulting solution was added HATU (0.207 g, 0.545 mmol). After stirring for 5 minutes, 5-amino-2-fluorobenzonitrile, (79.9 mg, 0.569 mmol ) was added, and the reaction mixture was stirred at room temperature for 20 hours. The reaction was next continued at 50°C for 4 hours. The volatiles were evaporated and the obtained residue was dissolved in CH2CI2 (2.5 mL) and purified by silica gel Chromatography (heptane-EtOAc 100/0 to 0/100) followed by repurification with CH2Cl2-MeOH 100/0 to 98/2 as eluent. The desired fractions were combined and evaporated, and co-evaporated with EtOAc. The residue was dried further at 50°C in vacuo, resulting in compound 191 (63 mg). Method F; Rt: 0.88 min. m/z: 420.1 (M-H)" Exact mass:421.1. 1H NMR (400 MHz, DMSO-d6) d ppm 1.46 (s, 3 H), 2.40 (s, 3 H), 4.19 (d, J=6.6 Hz, 2 H), 4.62 (d, J=6.2 Hz, 2 H), 7.36 (d, J=8.1 Hz, 1 H), 7.58 (t, J=9.1 Hz, 1 H), 7.80 (t, J=7.9 Hz, 1 H), 7.96 (ddd, J=9.1, 4.8, 2.8 Hz, 1 H), 8.22 (dd, J=5.7, 2.6 Hz, 1 H), 8.64 (s, 1 H), 11.16 (s, 1 H). 19F NMR (377 MHz, DMSO-de) δ ppm - 115.10 (d, J=7.9 Hz, 1 F), -113.61 (dt, J=8.9, 5.2 Hz, 1 F).
Synthesis of 3-chloro-4,5-difluoro-aniiine 3-chloro-4,5-difluorobenzoic acid (commercial from astatech, 25.5 g, 0.132 mol ) was dissolved in tert-butyl alcohol (200 mL) at 50°C. Et3N (20.2 mL, 0.146 mol ) was added. Diphenylphosphoryl azide, 30.0 mL, 0.139 mol ) was added slowly, and the reaction mixture was stirred and refluxed for 18 hours. The volatiles were evaporated, and co-evaporated with EtOAc. The residue was stirred in Et20 (300 mL)/Sat. NaHC03 (300 mL) /H20 (50 mL) for 15 minutes. The separated organic layer was dried with MgS04, filtered off, and evaporated. The solid residue was stirred in diisopropylether (20 mL), filtered off, washed with diisopropylether (3x) and dried at 50°C, resulting in tert-butyl N-(3-chloro-4,5-difluoro-phenyl)carbamate (8.5 g). The filtrate was concentrated in vacuo. The residue was stirred in CH2CI2 (20 mL) + heptanes (20 mL), filtered off, washed with CH2Cl2-heptane 1/1 (2x) and heptanes (2x), and dried at 50°C in vacuo, resulting in more tert-butyl N-(3-chloro-4,5-difluoro-phenyl)carbamate, 11.8 g). tert-butyl N-(3-chloro-4,5-difluoro-phenyl)carbamate (8.5 g, 0.0322 mol) was added portion wise to stirring HC1 (40 mL, 0.16 mol, 4 M in dioxane). The mixture was stirred at room tempertaure for 2 hours, then left standing for 65 hours. Stirring was continued for another 2 hours. The formed precipitate was filtered off , washed with dioxane (4x) and dried at 50°C in vacuo, resulting in 3-chloro-4,5-difluoro-aniline hydrochloride (5.95 g). A mixture of 3-chloro-4,5-difluoro-aniline hydrochloride (1 g, 0.005 mol), NaOH (1M in H20, 10 mL, 0.01 mol) and toluene (15 mL) was stirred at room temperature for 1 hour. The separated organic layer was dried with MgS04, filtered off, and evaporated. The obtained 3-chloro-4,5-difluoro-aniline (0.81 g) was used as such.
Compound 192
Figure imgf000105_0001
Compound 192 was prepared similarly as described for compound 191, using 3-chloro- 4,5-dif uoro-aniline hydrochloride instead of 5-amino-2-fluorobenzonitrile.19F NMR (377 MHz, DMSO-dg) d ppm -144.93 (br. s., 1 F), -134.02 - -133.17 (m, 1 F), -115.09 (d, J=7.9 Hz, 1 F). 1H NMR (400 MHz, DMSO-dg) δ ppm 1.45 (s, 3 H), 2.38 (s, 3 H), 4.18 (d, J=6.4 Hz, 2 H), 4.61 (d, J=6.2 Hz, 2 H), 7.35 (d, J=8.1 Hz, 1 H), 7.71 - 7.83 (m, 3 H), 8.64 (br. s., 1 H), 11.14 (br. s., 1 H). Method F; Rt: 1.05 min. m/z: 447.1 (M- H)~ Exact mass:448.0.
Figure imgf000105_0002
Oxalyl chloride (12.3 mL, 0.143 mol) was added dropwise to a stirring solution of 5- bromo-3-chlorosulfonyl-2-fluoro-6-methyl-benzoic acid (9.5 g) and DMF (0.111 mL) in CH2CI2 (100 mL). After addition, the reaction mixture was stirred at room
temperature for 2 hours and 30 minutes. The volatiles were removed in vacuo, and co- evaporated with toluene. The obtained residue containing 5-bromo-3-chlorosulfonyl-2- fluoro-6-methyl-benzoyl chloride was used as such. A solution of 5-bromo-3- chlorosulfonyl-2-fluoro-6-methyl-benzoyl chloride (1.75 g) in toluene (20 mL) was stirred at reflux under N2-flow. A solution of 3-chloro-4,5-difluoroaniline (0.818 g, 0.005 mol) in toluene (10 mL) was added dropwise. After addition, the reaction mixture was refluxed for 45 minutes, then allowed to reach room temperature, and left standing for 18 hours. A precipitate (0.51 g) was filtered off, washed with toluene (2 x), and dried at 50°C in vacuo. (R)- 1 , 1 ,1 -trifluoro-2-propylamine (0.181 g, 0.0016 mol ) was dissolved in CH3CN (5 mL ) under N2-atm. 5-bromo-3-[(3-chloro-4,5-difluoro- phenyl)carbamoyl]-2-fluoro-4-methyl-benzenesulfonyl chloride (0.51 g) was added, then DIPEA (0.461 mL, 0.00267 mol). The mixture was stirred in a sealed tube at 80°C for 20 hours. The reaction mixture was allowed to reach room temperature, and left standing for 2 hours. The mixture was filtered and the filtrate was evaporated. The residue was dissolved in CH2CI2 (2 mL), and purified by silica gel chromatography [heptane-EtOAc 100/0 to 0/100 ]. The fractions containing the desired compound were combined and evaporated, and co-evaporated with EtOH, resulting in crude 5-bromo- N-(3-chloro-4,5-difluoro-phenyl)-2-fluoro-6-methyl-3-[[(lR)-2,2,2-trifluoro-l-methyl- ethyl]sulfamoyl]benzamide (0.12 g).To a solution of 5-bromo-N-(3-chloro-4,5- difluoro-phenyl)-2-fluoro-6-methyl-3-[[(lR)-2,2,2-trifluoro-l-methyl- ethyl]sulfamoyl]benzamide (0.1 g) in EtOH (1 1 mL ) was added ¾0 (3.5 mL ), then K2CO3 aq. sat. sol, (1.25 mL) and next Palladium(0)tetrakis(triphenylphosphine (26.1 mg, 0.023 mmol). The mixture was stirred 150°C by microwave irradiation for 45 minutes. The reaction mixture was combined with a similar reaction mixture starting from 20 mg 5-bromo-N-(3-chloro-4,5-difluoro-phenyl)-2-fluoro-6-methyl-3-[[(lR)- 2,2,2-trifluoro-l-methyl-ethyl]sulfamoyl]benzamide) allowed to reach room
temperature and left standing for 15 minutes. The upper layer was isolated by means of a separation funnel, and evaporated. The obtained residue was purified by silica gel chromatography (heptane-EtOAc 100/0 to 0/100, also CH2Cl2-MeOH 100/0 to 98/2), followed by separation by preparative HPLC (Stationary phase: RP Vydac Denali CI 8 - ΙΟμπι, 200g, 5cm), Mobile phase: 0.25% NH4HCO3 solution in water, CH3CN) , resulting in compound 193 (1 1.4 mg). Method F; Rt: 1.17 min. m/z: 473.0 (M-H)~ Exact mass:474.0. 1H NMR (400 MHz, DMSO-d6) δ ppm 1.17 (d, J=6.8 Hz, 3 H), 2.38 (s, 3 H), 4.00-4.15 (m, 1 H), 7.35 (d, J=8.4 Hz, 1 H), 7.71 - 7.78 (m, 2 H), 7.82 (t, J=7.8 Hz, 1 H), 9.00 (br. s., 1 H), 1 1.13 (s, 1 H). 19F NMR (377 MHz, DMSO-de) d ppm - 145.3 to -144.5 (m, 1 F), -134.4 to -132.8 (m, 1 F), -1 14.9 (br. s., 1 F), -76.0 (d, J=7.2 Hz, 3 F). ompound 194
Figure imgf000107_0001
2-fluoro-6-methyl-3-[(3-methyloxetan-3-yl)sulfamoyl]benzoic acid (0.15 g, 0.473 mmol) was dissolved in DMF (5 mL) and triethylamine (0.2 mL) and HATU (233 mg, 0.61 mmol) were added to the reaction mixture. The reaction mixture was stirred for 10 minutes and 3,4-difluoroaniline (123 mg, 0.945 mmol) was added. The reaction mixture was stirred at room temperature for 42 hours. The reaction mixture was poured into ice water (50 mL). The mixture was extracted with Me-THF (3 x 20 mL). The combined organic extracts were washed with brine, dried (Na2S04) and concentrated. The residue was purified using silica gel column chromatography (ethyl acetate in heptane from 0 to 100% and methanol in dichloromethane from 0 to 2%) to afford compound 194 (79 mg) as a white powder which was dried in vacuum oven overnight. Method F; Rt: 0.94 min. m/z: 413.2 (M-H)~ Exact mass: 414.1. 1H NMR (400 MHz,
DMSO-dg) δ ppm 1.45 (s, 3 H), 2.39 (s, 3 H), 4.18 (d, J=6.6 Hz, 2 H), 4.62 (d, J=6.2 Hz, 2 H), 7.35 (d, J=8.1 Hz, 1 H), 7.39 - 7.51 (m, 2 H), 7.79 (t, J=7.8 Hz, 1 H), 7.87 (ddd, J=12.9, 7.4, 2.0 Hz, 1 H), 8.64 (br. s., 1 H), 11.00 (s, 1 H)
Compound 195
Figure imgf000107_0002
Compound 195 (98 mg) was prepared similarly as described for compound 194, using 3-chloro-4-fluoroaniline instead of 3,4-difluoroaniline. Method F; Rt: 0.99 min. m/z:
429.1 (M-H~)~ Exact mass:430.1. 1H NMR (400 MHz, DMSO-d6) δ ppm 1.45 (s, 3 H), 2.39 (s, 3 H), 4.18 (d, J=6.4 Hz, 2 H), 4.62 (d, J=6.2 Hz, 2 H), 7.35 (d, J=8.1 Hz, 1 H), 7.45 (t, J=9.0 Hz, 1 H), 7.60 (ddd, J=9.0, 4.3, 2.5 Hz, 1 H), 7.79 (t, J=7.9 Hz, 1 H), 8.02 (dd, J=6.8, 2.6 Hz, 1 H), 8.63 (br. s., 1 H), 10.99 (s, 1 H)
Compound 196
Figure imgf000108_0001
Sodium carbonate (2.07 g, 19.48 mmol) was dissolved in distilled water (30 mL). To this was added (5)-3-aminotetrahydrofuran (3.4 g, 38.97 mmol) at once followed by THF (30 mL). The obtained solution was stirred and cooled in an ice bath. 3- (chlorosulfonyl)-2,6-difluorobenzoic acid (5 g, 19.48 mmol) was dissolved in THF (40 mL) and this was added drop wise to the stirring solution. The resulting mixture was stirred for 30 minutes while cooling was continued. Then the mixture was stirred for 3 hours at room temperature. The mixture was concentrated in vacuo until only water remained. Water (20 mL) was added and the mixture was acidified with HCl (1M / aq; 40 mL). This was extracted using Me-THF (3 x 50 mL). The combined organics were washed with of brine (50 mL), dried on Na2S04, filtered and concentrated in vacuo yielding 2,6-difluoro-3-[[(3S)-tetrahydrofuran-3-yl]sulfamoyl]benzoic acid as a yellow powder (5.9 g). Method F, Rt: 0.33 min. m/z : 306.0 (M-H)~ Exact mass: 307.0. 2,6- difluoro-3-[[(3S)-tetrahydrofuran-3-yl]sulfamoyl]benzoic acid (1 g, 2.99 mmol) was dissolved in N,N-dimethylformamide (5 mL). HATU (1.42 g, 3.74 mmol) was added followed by diisopropylethylamine (1.55 mL, 8.98 mmol). The resulting mixture was stirred for 30 minutes at room temperature. Then, 3,4-difluoroaniline (0.77 g, 5.99 mmol) was added. The resulting mixture was stirred for 24 hours and next poured in water (50 mL) and extracted using Me-THF (3 x 50 mL). The combined organics were washed with brine, dried on Na2S04, filtered and concentrated in vacuo. The obtained residue was purified by silica gel column chromatography using gradient elution from heptane to EtOAc. (100:0 to 0:100). The desired fractions were concentrated in vacuo and dried in a vacuum oven at 55°C for 24 hours yielding compound 196. Method F, Rt: 0.92 min. m/z : 417.1 (M-H)" Exact mass: 418.1. 1H NMR (400 MHz, DMSO-d6) δ ppm 1.64 - 1.79 (m, 1 H), 1.92 - 2.07 (m, 1 H), 3.43 (dd, J=9.0, 4.6 Hz, 1 H), 3.56 - 3.79 (m, 3 H), 3.80 - 3.92 (m, 1 H), 7.32 - 7.43 (m, 1 H), 7.44 - 7.54 (m, 2 H), 7.84 (ddd, J=12.7, 7.4, 2.5 Hz, 1 H), 8.01 (td, J=8.6, 6.2 Hz, 1 H), 8.49 (br. s., 1 H), 11.21 (br. s., 1 H) Compound 197 to 201 were prepared as described for compound 196, using the corresponding aniline instead of 3,4-difluoroaniline:
Compound 197
Figure imgf000109_0001
4-fluoro-3-methylaniline was used as aniline. 1H NMR (400 MHz, DMSO-d6) δ ppm 1.64 - 1.76 (m, 1 H), 1.91 - 2.05 (m, 1 H), 2.25 (d, J=1.8 Hz, 3 H), 3.42 (dd, J=8.9, 4.7 Hz, 1 H), 3.56 - 3.78 (m, 3 H), 3.79 - 3.88 (m, 1 H), 7.16 (t, J=9.1 Hz, 1 H), 7.41 - 7.51 (m, 2 H), 7.60 (dd, J=7.0, 2.2 Hz, 1 H), 7.97 (td, J=8.6, 6.2 Hz, 1 H), 8.49 (br. s, 1 H), 10.93 (s, 1 H). Method F, Rt: 0.93 min. m/z : 413.2 (M-H)- Exact mass: 414.1
Compound 198
Figure imgf000109_0002
3-bromo-4-fluoroaniline was used as aniline. Method G, Rt: 1.74 min. m/z : 478.8 (M- H)~ Exact mass: 480.0. 1 H NMR (400 MHz, DMSO-d6) δ ppm 1.67 - 1.77 (m, 1 H),
I .93 - 2.05 (m, 1 H), 3.43 (dd, J=9.0, 4.6 Hz, 1 H), 3.57 - 3.78 (m, 3 H), 3.80 - 3.89 (m, 1 H), 7.43 (t, J=8.7 Hz, 1 H), 7.49 (m, J=8.7, 8.7 Hz, 1 H), 7.61 (ddd, J=9.0, 4.4, 2.6 Hz, 1 H), 8.00 (td, J=8.6, 6.2 Hz, 1 H), 8.11 (dd, J=6.3, 2.5 Hz, 1 H), 8.49 (br. s., 1 H),
I I .19 (br. s., 1 H)
Compound 199
Figure imgf000109_0003
5-amino-2-fluorobenzonitrile was used as aniline
Method G, Rt: 1.56 min. m/z : 423.9 (M-H)" Exact mass: 425.1. 1 H NMR (400 MHz, DMSO-de) δ ppm 1.65-1.80 (m, 1 H), 1.94 - 2.06 (m, 1 H), 3.43 (dd, J=9.0, 4.6 Hz, 1 H), 3.57 - 3.78 (m, 3 H), 3.80 - 3.91 (m, 1 H), 7.49 (t, J=8.5 Hz, 1 H), 7.59 (t, J=9.1 Hz, 1 H), 7.94 (ddd, J=9.2, 4.8, 2.6 Hz, 1 H), 8.02 (td, J=8.6, 6.2 Hz, 1 H), 8.19 (dd, J=5.7, 2.9 Hz, 1 H), 8.50 (br. s., 1 H), 11.37 (br. s., 1 H).
Compound 200
Figure imgf000110_0001
4-fluoro-3-(trifluoromethyl)aniline was used as aniline
Method F, Rt: 1.02 min. m/z : 467.1 (M-H)- Exact mass: 468.1. 1H NMR (400 MHz, DMSO- g) δ ppm 1.72 (ddt, J=12.6, 7.2, 5.6, 5.6 Hz, 1 H), 1.93 - 2.08 (m, 1 H), 3.43 (dd, J=9.0, 4.6 Hz, 1 H), 3.58 - 3.79 (m, 3 H), 3.80 - 3.91 (m, 1 H), 7.49 (t, J=8.4 Hz, 1 H), 7.58 (t, J=9.7 Hz, 1 H), 7.93 (s, 1 H), 8.02 (td, J=8.6, 6.2 Hz, 1 H), 8.16 (dd, J=6.4, 2.6 Hz, 1 H), 8.50 (br. s., 1 H), 11.35 (br. s., 1 H)
Compound 201
Figure imgf000110_0002
3-chloro-4-fluoroaniline was used as aniline.
Method F, Rt: 0.97 min. m/z: 433.1 (M-H)- Exact mass: 434.0. 1H NMR (400 MHz, DMSC /g) δ ppm 1.72 (ddt, J=12.5, 7.2, 5.6, 5.6 Hz, 1 H), 1.92 - 2.12 (m, 1 H), 3.43 (dd, J=8.8, 4.6 Hz, 1 H), 3.55 - 3.79 (m, 3 H), 3.80 - 3.91 (m, 1 H), 7.35 - 7.52 (m, 2 H), 7.53 - 7.67 (m, 1 H), 7.90 - 8.12 (m, 2 H), 8.49 (br. s., 1 H), 11.20 (br. s., 1 H)
Compound 202 and 203 were prepared similarly as described for compound 196, using isopropyl amine instead of (5)-3-aminotetrahydrofuran and for compound 203, using 3- (trifluoromethyl)aniline instead of 3,4-difluoroaniline.
Compound 202
Figure imgf000110_0003
Method G, Rt: 1.80 min. m/z : 388.9 (M-H)- Exact mass: 390.1.
1 H NMR (400 MHz, DMSO-d6) δ ppm 1.03 (d, J=6.6 Hz, 8 H), 3.34 - 3.46 (m, 1 H), 7.36 - 7.53 (m, 3 H), 7.84 (ddd, J=12.7, 7.4, 2.5 Hz, 1 H), 8.00 (td, J=8.6, 6.2 Hz, 1 H), 8.09 (br. s., 1 H), 11.20 (br. s., 1 H) ompound 203
Figure imgf000111_0001
Method G, Rt: 1.82 min. m/z : 421.1 (M-H)- Exact mass: 422.1. 1 H NMR (400 MHz, DMSO-dg) δ ppm 1.04 (d, J=6.6 Hz, 6 H), 3.34 - 3.46 (m, 1 H), 7.47 (t, J=8.6 Hz, 1 H), 7.54 (d, J=7.9 Hz, 1 H), 7.65 (t, J=7.9 Hz, 1 H), 7.87 (d, J=8.4 Hz, 1 H), 8.01 (td, J=8.6, 6.2 Hz, 1 H), 8.11 (d, J=7.5 Hz, 1 H), 8.15 (s, 1 H), 11.32 (s, 1 H).
Compound 204
Figure imgf000111_0002
Compound 204 (0.19 g) was prepared starting from compound 190 (0.34 g), similar as described for the conversion of compound 187 to compound 188. Compound 204 was crystallised from Et20, filtered off, washed with 3x Et20, and dried at 50°C in vacuo. Method F; Rt: 0.94 min. m/z: 409.1 (M-H)" Exact mass:410.1. 1H NMR (400 MHz, DMSO-dg) δ ppm 1.46 (s, 3 H), 2.24 (d, J=1.8 Hz, 3 H), 2.38 (s, 3 H), 4.18 (d, J=6.6 Hz, 2 H), 4.62 (d, J=6.2 Hz, 2 H), 7.14 (dd, J=9.1 Hz, 1 H), 7.33 (d, J=8.1 Hz, 1 H), 7.45 - 7.53 (m, 1 H), 7.63 (dd, J=7.0, 2.2 Hz, 1 H), 7.77 (t, J=7.9 Hz, 1 H), 8.61 (br. s., 1 H), 10.72 (s, 1 H). Compound 205
Figure imgf000111_0003
3-(tert-butylsulfamoyl)-2-fluoro-6-methyl-benzoic acid was prepared similarly as described for 2-fluoro-6-methyl-3-[(3-methyloxetan-3-yl)sulfamoyl]benzoic acid, using tert-butylamine instead of 3-methyloxetan-3-amine. Compound 205 was prepared similar as described for compound 194, using 4-fluoro-3-methylaniline instead of 3,4- difluoroaniline and starting from 3-(tert-butylsulfamoyl)-2-fluoro-6-methyl-benzoic acid instead of 2-fluoro-6-methyl-3-[(3-methyloxetan-3-yl)sulfamoyl]benzoic acid. Method F; Rt: 1.08 min. m/z: 395.2 (M-H)" Exact mass: 396.1.1H NMR (400 MHz, DMSO-dg) δ ppm 1.16 (s, 9 H), 2.24 (d, J=1.8 Hz, 3 H), 2.37 (s, 3 H), 7.14 (t, J=9.2 Hz, 1 H), 7.30 (d, J=8.1 Hz, 1 H), 7.50 (ddd, J=9.0, 4.7, 2.3 Hz, 1 H), 7.64 (dd, J=6.9, 2.3 Hz, 1 H), 7.73 - 7.84 (m, 2 H), 10.70 (br. s, 1 H).
Compound 206
Figure imgf000112_0001
Compound 206 was prepared similar as described for for compound 194, starting from 3-(tert-butylsulfamoyl)-2-fluoro-6-methyl-benzoic acid instead of 2-fluoro-6-methyl-3- [(3-methyloxetan-3-yl)sulfamoyl]benzoic acid. Method F; Rt: 1.08 min. m/z: 399.1 (M- H)~ Exact mass:400.1. 1H NMR (400 MHz, DMSO-d6) δ ppm 1.16 (s, 9 H), 2.31 (s, 3 H), 7.32 (d, J=8.1 Hz, 1 H), 7.40 - 7.51 (m, 2 H), 7.76 - 7.82 (m, 2 H), 7.88 (ddd, J=13.0, 7.5, 2.4 Hz, 1 H), 10.97 (br. s., 1 H)
Synthesis of 6-chloro-2-fluoro-3-[(3-methyloxetan-3-yl)sulfamoyl]benzoic acid and 2- chloro-6-fluoro-3-[(3-methyloxetan-3-yl)sulfamoyl]benzoic acid
2-chloro-6-fluorobenzoic acid (2 g, 11.46 mmol) was treated with chlorosulfonic acid (10 mL, 150.44 mmol) and this was heated to 100°C and stirred for 5 hours. The resulting mixture was cooled to room temperature and added dropwise to ice-water (1 liter). This was then extracted using dichloromethane (2 x 500 mL). The combined organics were dried on Na2S04, filtered and concentrated in vacuo yielding an isomeric mixture of 2-chloro-3-chlorosulfonyl-6-fluoro-benzoic acid and 6-chloro-3- chlorosulfonyl-2-fluoro-benzoic acid (3.1 gram) as a slightly yellow powder which was used as such.Method F, Rt: 0.47 min and 0.49 min. m/z : 270.9 (M-H)- Exact mass: 271.9. Sodium carbonate (1.21 g, 11.4 mmol) was dissolved in distilled water (22 mL). To this was added 3-methyl-3-oxetanamine (1.19 g, 13.68 mmol) at once followed by THF (20 mL). The obtained solution was stirred and cooled in an ice bath. An isomeric mixture of 2-chloro-3-chlorosulfonyl-6-fluoro-benzoic acid and 6-chloro-3- chlorosulfonyl-2-fluoro-benzoic acid (3.1 g, 11.4 mmol) was dissolved in THF (30 mL) and this was added drop wise to the stirring solution. The resulting mixture was stirred for 30 minutes while cooling was continued. Then, the mixture was stirred for 3 hours at room temperature.The mixture was concentrated in vacuo untill only water remained. Then water (20 mL) was added and the mixture was acidified with HC1 (46 mL, 1M / aq). This was extracted using Me-THF (3 X 50 mL). The combined organics were dried on Na2S04, filtered and concentrated in vacuo. The residue was purified, and isomers were separated using preparative HPLC (Stationary phase: Uptisphere CI 8 ODB - ΙΟμηι, 200g, 5cm), Mobile phase: 0.25% NH4HC03 solution in water, MeOH) , yielding 6-chloro-2-fluoro-3-[(3-methyloxetan-3-yl)sulfamoyl]benzoic acid as a white powder. Method G, Rt: 0.40 min. m/z : 322.0 (M-H)" Exact mass: 323.0. 1H NMR (400 MHz, DMSO-d ) ppm 1.42 (s, 3 H), 4.15 (d, J=6.6 Hz, 2 H), 4.61 (d, J=5.9 Hz, 13 H), 7.29 (dd, J=8.5, 0.8 Hz, 1 H), 7.36 - 7.73 (m, 5 H).
and 2-chloro-6-fluoro-3-[(3-methyloxetan-3-yl)sulfamoyl]benzoic acid as a white powder. Method G, Rt: 0.34 min. m/z : 321.9 (M-H)" Exact mass: 323.0
Compound 207 to 210 were prepared similarly as described for compound 196 using 6- chloro-2-fluoro-3-[(3-methyloxetan-3-yl)sulfamoyl]benzoic acid instead of 2,6- difluoro-3-[[(35)-tetrahydrofuran-3-yl]sulfamoyl]benzoic acid and the corresponding aniline instead of 3,4-difluoroaniline. Compound 207
Figure imgf000113_0001
Using 5-amino-2-fluorobenzonitrile as aniline. Method F, Rt: 0.92 min. m/z : 440.0 (M- H)" Exact mass: 441.0. 1H NMR (400 MHz, DMSO-d6) δ ppm 1.46 (s, 2 H), 4.21 (d, J=6.4 Hz, 2 H), 4.61 (d, J=6.2 Hz, 2 H), 7.59 (t, J=9.1 Hz, 1 H), 7.66 (d, J=8.8 Hz, 1 H), 7.89 - 7.99 (m, 2 H), 8.18 (dd, J=5.6, 2.8 Hz, 1 H), 8.93 (br. s, 1 H), 11.37 (br. s., 1 H)
Figure imgf000113_0002
Using 4-fluoro-3-(trifluoromethyl)aniline as aniline. Method F, Rt: 1.06 min. m/z : 483 (M-H)" Exact mass: 484.0. 1H NMR (400 MHz, DMSO-d6) δ ppm 1.46 (s, 2 H), 4.20 (d, J=6.2 Hz, 2 H), 4.61 (d, J=6.2 Hz, 2 H), 7.58 (t, J=9.9 Hz, 1 H), 7.66 (d, J=8.6 Hz, 1 H), 7.94 (m, J=8.1, 8.1 Hz, 2 H), 8.07 - 8.25 (m, 1 H), 8.91 (br. s, 1 H), 11.34 (br. s., 1 H) Compound 209
Figure imgf000114_0001
Using 3,4-difluoro-5-methyl-aniline as aniline. Method F, Rt: 1.03 min. m/z : 447.1 (M-H)~ Exact mass: 448.1. 1H NMR (400 MHz, DMSO-d6) δ ppm 1.45 (s, 3 H), 2.30 (d, J=2.0 Hz, 3 H), 4.20 (d, J=6.4 Hz, 2 H), 4.61 (d, J=6.2 Hz, 2 H), 7.32 (m, J=5.9 Hz, 1 H), 7.54 - 7.69 (m, 2 H), 7.91 (t, J=8.3 Hz, 1 H), 8.92 (br. s, 1 H), 11.09 (br. s, 1 H) Compound 210
Figure imgf000114_0002
Using 3-chloro-4,5-difluoro-aniline hydrochloride as aniline. Method F, Rt: 1.07 min. m/z : 467.0 (M-H)~ Exact mass: 468.0. 1H NMR (400 MHz, DMSO-d6) δ ppm 1.45 (s 3 H), 4.20 (d, J=6.6 Hz, 2 H), 4.60 (d, J=6.2 Hz, 2 H), 7.64 (d, J=8.6 Hz, 1 H), 7.67 - 7.79 (m, 2 H), 7.93 (t, J=8.1 Hz, 1 H), 9.08 (br. s, 1 H), 11.34 (br. s., 1 H)
Compound 211
Figure imgf000114_0003
Compound 211 was prepared similarly as described for compound 196 using 2-chloro- 6-fluoro-3-[(3-methyloxetan-3-yl)sulfamoyl]benzoic acid instead of 2,6-difluoro-3- [[(35)-tetrahydrofuran-3-yl]sulfamoyl]benzoic acid. Method F, Rt: 0.94 min. m/z : 433.1 (M-H)" Exact mass: 434.0. 1H NMR (400 MHz, DMSO-d6) δ ppm 1.46 (s, 3 H), 4.20 (d, J=6.6 Hz, 2 H), 4.62 (d, J=6.4 Hz, 2 H), 7.30 - 7.43 (m, 1 H), 7.43 - 7.54 (m, 1
H), 7.61 (t, J=8.6 Hz, 1 H), 7.84 (ddd, J=12.7, 7.4, 2.3 Hz, 1 H), 8.17 (dd, J=9.0, 5.9 Hz, 1 H), 8.75 (br. s, 1 H), 11.18 (br. s, 1 H). 2-bromo-6-fluoro-3-[(3-methyloxetan-3-yl)sulfamoyl]benzoic acid and 6-bromo-2- fluoro-3-[(3-methyloxetan-3-yl)sulfamoyl]benzoic acid were prepared similarly as described for 2-chloro-6-fluoro-3-[(3-methyloxetan-3-yl)sulfamoyl]benzoic acid and 6- chloro-2-fluoro-3-[(3-methyloxetan-3-yl)sulfamoyl]benzoic acid, starting from 2- bromo-6-fluorobenzoic acid instead of 2-chloro-6-fluorobenzoic acid.
Compound 212
Figure imgf000115_0001
Compound 212 was prepared similarly as described for compound 196 using 2-bromo- 6-fluoro-3-[(3-methyloxetan-3-yl)sulfamoyl]benzoic acid instead of 2,6-difluoro-3- [[(35)-tetrahydrofuran-3-yl]sulfamoyl]benzoic acid and 4-fluoro-3- (trifluoromethyl)aniline instead of 3,4-difluoroaniline. 1 H NMR (400 MHz, DMSO-d6) δ ppm 1.48 (s, 3 H), 4.20 (d, J=6.6 Hz, 2 H), 4.64 (d, J=6.2 Hz, 2 H), 7.57 (t, J=9.7 Hz, 1 H), 7.65 (t, J=8.6 Hz, 1 H), 7.93 (dt, J=8.4, 3.7 Hz, 1 H), 8.08 - 8.31 (m, 2 H), 8.70 (br. s., 1 H), 11.29 (br. s., 1 H).
Compound 213 to 216 were prepared similarly as described for compound 196 using 6- bromo-2-fluoro-3-[(3-methyloxetan-3-yl)sulfamoyl]benzoic acid instead of 2,6- difluoro-3-[[(35)-tetrahydrofuran-3-yl]sulfamoyl]benzoic acid the corresponding aniline instead of 3,4-difluoroaniline.
Compound 213
Figure imgf000115_0002
Using 4-fluoro-3-methylaniline as aniline. Method F, Rt: 0.99 min. m/z: 473.0 (M-H)~ Exact mass: 474.0. 1H NMR (400 MHz, DMSO-de) δ ppm 1.46 (s, 3 H), 2.25 (d, J=1.5 Hz, 3 H), 4.20 (d, J=6.4 Hz, 2 H), 4.62 (d, J=6.2 Hz, 2 H), 7.16 (t, J=9.1 Hz, 1 H), 7.42 - 7.52 (m, 1 H), 7.60 (dd, J=7.0, 2.4 Hz, 1 H), 7.68 - 7.93 (m, 2 H), 8.65 (br. s, 1 H), 10.82 (br. s, 1 H). Compound 214
Figure imgf000116_0001
Using 5-amino-2-fluorobenzonitrile as aniline. Method F, Rt: 0.92 min. m/z : 484.0 (M- H)~ Exact mass: 485.0. 1H NMR (400 MHz, DMSO-dg) δ ppm 1.39 - 1.55 (m, 3 H), 4.20 (d, J=6.6 Hz, 2 H), 4.61 (d, J=6.4 Hz, 2 H), 7.59 (t, J=9.1 Hz, 1 H), 7.77 - 7.89 (m, 2 H), 7.95 (ddd, J=9.2, 4.8, 2.8 Hz, 1 H), 8.18 (dd, J=5.7, 2.6 Hz, 1 H), 8.90 (br. s, 1 H), 11.34 (br. s., 1 H).
Compound 215
Figure imgf000116_0002
Using 4-fluoro-3-(trifluoromethyl)aniline as aniline. Method F,Rt: 1.07 min. m/z :
527.0 (M-H)~ Exact mass: 528.0. 1H NMR (400 MHz, DMSO-dg) δ ppm 1.46 (s, 3 H), 4.20 (d, J=6.6 Hz, 2 H), 4.61 (d, J=6.2 Hz, 2 H), 7.58 (t, J=9.8 Hz, 1 H), 7.74 - 7.89 (m, 2 H), 7.90 - 7.98 (m, 1 H), 8.16 (dd, J=6.3, 2.5 Hz, 1 H), 8.84 (br. s, 1 H), 11.31 (br. s., 1 H).
Compound 216
Figure imgf000116_0003
Using 3,4-difluoro-5-methyl-aniline as aniline. Method F, Rt: 1.03 min. m/z : 491.0 (M-H)~ Exact mass: 492.0. 1H NMR (400 MHz, DMSO-dg) δ ppm 1.46 (s, 3 H), 2.30 (d, J=1.8 Hz, 3 H), 4.20 (d, J=6.6 Hz, 2 H), 4.61 (d, J=6.4 Hz, 2 H), 7.32 (m, J=5.7 Hz, 1 H), 7.61 (ddd, J=12.3, 6.9, 2.6 Hz, 1 H), 7.72 - 7.89 (m, 2 H), 8.86 (br. s., 1 H), 11.07 (br. s, 1 H).
Compound 217
Figure imgf000117_0001
A solution of 3-(difluoromethyl)-4-fluoro-aniline (1.02 mL, 8.58 mmol)
in dry toluene (10 mL) was added dropwise (over 15 min) to a refluxing solution of 5- chloro-3-chlorosulfonyl-2-fluoro-benzoyl chloride (2500 mg, 8.576 mmol) in dry toluene (100 mL). After the addition, the reaction mixture was left to stir at reflux for 1 h. The reaction mixture was left to cool to room temperature under nitrogen atmosphere while stirring.The brown solution containing 5-chloro-3-[[3-(difluoromethyl)-4-fluoro- phenyl]carbamoyl]-2-fluoro-benzenesulfonyl chloride was used without further purification. 3-methyl-3-oxetanamine (580 mg, 6.66 mmol) was added dropwise to the above solution at room temperature. Et3N (2.10 mL 15.14 mmol) was then added dropwise to the reaction mixture and the reaction mixture was stirred at room temperature for 45 minutes. The solvent was evaporated and the residue was taken up in EtOAc. HC1 (0.5 N, 30 mL) was added to the reaction mixture and the layers were separated. The organic layer was washed again with NaOH (0.5 N, 30 mL).
The organic layer was dried on MgSC^ and was evaporated. The obtained residue was purified by silica gel column chromatography (eluent:
Figure imgf000117_0002
100:0 -> 95:5), resulting in compound 217 (1.8 g). 1H NMR (360 MHz, DMSO-d6) δ ppm 1.45 (s, 3 H) 4.23 (d, J=6.2 Hz, 2 H) 4.63 (d, J=6.2 Hz, 2 H) 7.27 (t, J=54.3 Hz, 1 H) 7.43 (t,
J=9.7 Hz, 1 H) 7.83 (dt, J=8.1, 4.0 Hz, 1 H) 7.95 (dd, J=5.9, 2.6 Hz, 1 H) 8.04 (dd, J=6.0, 2.4 Hz, 1 H) 8.13 (dd, J=5.3, 2.7 Hz, 1 H) 8.98 (s, 1 H) 10.98 (s, 1 H)
Method F, Rt: 1.03 min. m/z : 465.1 (M-H)~ Exact mass: 466.0.
Compound 218
Figure imgf000117_0003
Pd/C (10%) (716 mg) was suspended in a solution of compound 217 (345 mg, 0.673 mmol) and Et3N (0.467 mL) in MeOH (100 mL) at room temperature under nitrogen atmosphere. The reaction mixture was next stirred at room temperature under an atmosphere of hydrogen until one equivalent of hydrogen was absorbed.The reaction mixture was filtered on decalite and the solvent was evaporated.The obtained residue was purified by silica gel column chromatography (CH2Ci2:MeOH 100:0 -> 95:5) resulting in compound 218 (206 mg) as a white solid, dried in vacuo at 50 °C.
1H NMR (360 MHz, DMSO-de ) δ ppm 1.44 (s, 3 H) 4.19 (d, J=6.6 Hz, 2 H) 4.63 (d, J=6.2 Hz, 2 H) 7.26 (t, J=54.3 Hz, 1 H) 7.42 (t, J=9.5 Hz, 1 H) 7.52 (t, J=7.7 Hz, 1 H) 7.86 (dd, J=8.1, 3.7 Hz, 1 H) 7.93 - 8.01 (m, 2 H) 8.06 (dd, J=6.4, 2.4 Hz, 1 H) 8.77 (s 1 H) 10.92 (s, 1 H). Method F, Rt: 0.92 min. m/z : 431.1 (M-H)~ Exact mass: 432.1.
Compound 219
Figure imgf000118_0001
Compound 219 (828 mg), was prepared similar as described for compound 217 and 218. Using 4-fluoro-3-(trifluoromethyl)aniline instead of 3-(difluoromethyl)-4-fluoro- aniline. Method F, Rt: 1.00 min. m/z : 449.1 (M-H)~ Exact mass: 450.1.
1H NMR (360 MHz, DMSO-de) δ ppm 1.44 (s, 3 H) 4.19 (d, J=5.9 Hz, 2 H) 4.62 (d, J=6.2 Hz, 2 H) 7.53 (t, J=7.9 Hz, 1 H) 7.57 (t, J=9.9 Hz, 1 H) 7.94 - 8.02 (m, 3 H) 8.20 (dd, J=6.4, 2.7 Hz, 1 H) 8.78 (s, 1 H) 11.02 (s, 1 H).
Compound 220
Figure imgf000118_0002
Compound 220 was prepared similar as described for compound 217 and 218, using (5)-3-aminotetrahydrofuran instead of 3-methyl-3-oxetanamine. Method F, Rt: 0.90 min. m/z : 431.1 (M-H)" Exact mass: 432.1. 1H NMR (360 MHz, DMSO-d6 ) δ ppm
1.66 - 1.77 (m, 1 H) 1.91 - 2.03 (m, 1 H) 3.43 (dd, J=8.8, 4.8 Hz, 1 H) 3.57 - 3.70 (m, 2 H) 3.70 - 3.78 (m, 1 H) 3.79 - 3.90 (m, 1 H) 7.26 (t, J=54.2 Hz, 1 H) 7.42 (t, J=9.5 Hz, 1 H) 7.53 (t, J=7.7 Hz, 1 H) 7.81 - 7.88 (m, 1 H) 7.94 - 8.00 (m, 2 H) 8.07 (dd, J=6.4, 2.4 Hz, 1 H) 8.45 (d, J=6.6 Hz, 1 H) 10.92 (s, 1 H).
Compound 221
Figure imgf000119_0001
Compound 221 was prepared similar as described for compound 217 and 218, using 2- methylpropan-2-amine instead of 3-methyl-3-oxetanamine, and 4-fluoro-3 -methyl- aniline instead of 3-(difluoromethyl)-4-fluoro-aniline Method F, Rt: 1.06 min. m/z :
381.2 (M-H)" Exact mass: 382.1. 1 H NMR (360 MHz, DMSO-d6) δ ppm 1.15 (s, 9 H) 2.24 (d, J=1.5 Hz, 3 H) 7.15 (t, J=9.1 Hz, 1 H) 7.47 (t, J=7.7 Hz, 1 H) 7.43 - 7.55 (m, 1 H) 7.65 (dd, J=7.0, 2.6 Hz, 1 H) 7.87 (ddd, J=7.8, 6.1, 1.8 Hz, 1 H) 7.93 (s, 1 H) 7.90 - 7.99 (m, 1 H) 10.63 (s, 1 H).
Compound 243
Figure imgf000119_0002
Compound 243 was prepared similar as described for compound 217 and 218, using tert-butylamine instead of 3-methyl-3-oxetanamine. Method G, Rt: 1.76 min. m/z : 417.1 (M-H)" Exact mass: 418.1. 1H NMR (360 MHz, DMSO-d6 ) δ ppm 1.15 (s, 9 H) 7.41 (t, J=9.7 Hz, 1 H) 7.26 (t, J=54.5 Hz, 1 H) 7.49 (t, J=7.7 Hz, 1 H) 7.85 (ddd, J=8.6, 4.4, 3.1 Hz, 1 H) 7.88 - 8.01 (m, 3 H) 8.08 (dd, J=6.2, 2.6 Hz, 1 H) 10.90 (s, 1 H).
Compound 222
Figure imgf000119_0003
Compound 222 was prepared similar as described for compound 221, using 3-methyl- 3-oxetanamine instead of 2-methylpropan-2-amine. Method F, Rt: 0.91 min. m z : 395.1 (M-H)" Exact mass: 396.1. 1 H NMR (360 MHz, DMSO-d6) δ ppm 1.44 (s, 3 H) 2.24 (d, J=1.5 Hz, 3 H) 4.19 (d, J=6.6 Hz, 2 H) 4.62 (d, J=6.2 Hz, 2 H) 7.15 (t, J=9.3 Hz, 1 H) 7.46 - 7.55 (m, 2 H) 7.63 (dd, J=7.0, 2.6 Hz, 1 H) 7.88 - 7.99 (m, 2 H) 8.75 (s, 1 H) 10.65 (s, 1 H).
Figure imgf000120_0001
3-methyloxolan-3-amine hydrochloride (165.9 mg, 1.21 mmol) was added to a solution of 3-[(4-fluoro-3-methyl-phenyl)carbamoyl]benzenesulfonyl chloride (499 mg, 1.096 mmol) in dry CH2CI2 (20 mL) at room temperature. Et3N (381 μί) was then added dropwise to the reaction mixture and the reaction mixture was stirred at room temperature for 1 hour. The reaction mixture was diluted with EtOAc (250 mL).
HC1 0.5 N (50 mL) was added and the layers were separated. The organic layer was washed again with NaOH 0.5 N (30 mL). The organic layer was dried on MgS04 and was evaporated. The obtained residue was purified t by silica gel column
chromatography (CH2Cl2:MeOH 100:0 -> 95:5) and by preparative HPLC (Stationary phase: RP XBridge Prep C18 ΟΒϋ-10μιη,30χ150ιηιη), Mobile phase: 0.25%
NH4HC03 solution in water, MeOH) resulting in compound 223 (257 mg) as a white solid after drying in vacuo at 50°C. Method F, Rt: 0.93 min. m/z : 391.2 (M-H)" Exact mass: 392.1.1 H NMR (360 MHz, DMSO-d6) ppm 1.17 (s, 3 H) 1.72 (dt, J=12.8, 7.7 Hz, 1 H) 2.14 (ddd, J=12.8, 7.1, 6.0 Hz, 1 H) 2.25 (d, J=1.8 Hz, 3 H) 3.30-3.40 (m, 1 H) 3.61 - 3.77 (m, 3 H) 7.15 (t, J=9.3 Hz, 1 H) 7.55 - 7.64 (m, 1 H) 7.69 (dd, J=7.0, 2.2 Hz, 1 H) 7.75 (t, J=7.9 Hz, 1 H) 8.04 (d, J=8.0 Hz, 1 H) 8.10 (br. s., 1 H) 8.18 (dt, J=7.7, 1.3 Hz, 1 H) 8.39 (t, J=1.6 Hz, 1 H) 10.49 (br. s., 1 H).
Compound 225
Figure imgf000120_0002
3-[(4-fluoro-3-methyl-phenyl)carbamoyl]benzenesulfonyl chloride (0.5 g, 1.53 mmol) and (i?)-l,l,l-trifluoro-2-propylamine (0.38 g, 3.36 mmol) were dissolved in of dichloromethane (10 mL). Then diisopropylethylamine (0.66 mL, 3.81 mmol) was added and the resulting mixture was stirred for two hours. Then 1M HC1 (5 mL) was added and the organic layer was separated, loaded on silica and subjected to silica gel column chromatography using gradient elution from heptane to EtOAc. (100:0 to 0: 100). The desired fractions were concentrated in vacuo and dried in a vacuum oven at 55°C for 24 hours compound 225 (233 mg) as a white powder. Method F, Rt: 1.05 min. m/z : 403.1 (M-H)~ Exact mass: 404.1. 1H NMR (400 MHz, DMSO-d6) δ ppm 1.01 (d, J=6.8 Hz, 3 H), 2.25 (d, J=1.8 Hz, 3 H), 4.06 - 4.22 (m, 1 H), 7.15 (t, J=9.2 Hz, 1 H), 7.51 - 7.63 (m, 1 H), 7.67 (dd, J=7.2, 2.3 Hz, 1 H), 7.78 (t, J=7.8 Hz, 1 H), 8.00 - 8.10 (m, 1 H), 8.16 - 8.28 (m, 1 H), 8.40 (t, J=1.7 Hz, 1 H), 8.66 (br. s., 1 H), 10.46 (s, 1 H).
Compound 226
Figure imgf000121_0001
Compound 226 (416 mg) was prepared as described for compound 225, using (S)- l , l , l-trifluoro-2-propylamine instead of (i?)-l , l ,l-trifluoro-2-propylamine. Method F, Rt: 1.05 min. m/z : 403.1 (M-H)~ Exact mass: 404.1.
Compound 227
Figure imgf000121_0002
Compound 227 (444 mg) was prepared similarly as described in synthetic procedure S3 (using 2,2-difluoroethylamine as amine), workup W4. Method F, Rt: 0.93 min. m/z : 371.1 (M-H)" Exact mass: 372.1. 1 H NMR (400 MHz, DMSO-d6 ) δ ppm 2.25 (d, J=1.8 Hz, 3 H), 3.26 (td, J=15.8, 3.7 Hz, 2 H), 6.00 (tt, J=55.2, 3.5 Hz, 1 H), 7.14 (t, J=9.0 Hz, 1 H), 7.52 - 7.62 (m, 1 H), 7.63 - 7.70 (m, 1 H), 7.77 (t, J=7.9 Hz, 1 H), 7.96 - 8.06 (m, 1 H), 8.14 - 8.25 (m, 1 H), 8.30-8.45 (m, 2 H), 10.46 (s, 1 H)
Compound 228
Figure imgf000121_0003
Compound 228 (238 mg) was prepared similarly as described in synthetic procedure S3 (using 2,2-difluoroethylamine as amine), workup W4, followed by preparative HPLC (SunFire Prep C18 ΟΒϋ-10μιη,30χ150ιηιη). Mobile phase (0.25% NH4HCO3 solution in water, MeOH). Method F, Rt: 0.97 min. m/z : 389.1 (M-H)~ Exact mass: 390.1.
1 H NMR (400 MHz, DMSO-d6) δ ppm 2.25 (d, J=1.8 Hz, 3 H), 3.74 (q, J=9.5 Hz, 2 H), 7.15 (t, J=9.2 Hz, 1 H), 7.48 - 7.62 (m, 1 H), 7.64 - 7.71 (m, 1 H), 7.77 (t, J=7.8 Hz, 1 H), 7.94 - 8.10 (m, 1 H), 8.20 (m, J=8.1 Hz, 1 H), 8.37 (t, J=1.7 Hz, 1 H), 8.49 - 9.15 (bs, 1 H), 10.45 (s, 1 H)
Compound 229
Figure imgf000122_0001
Compound 243 (239 mg) was prepared similar to synthetic procedure S2 (using 3,3- difluoro-cyclopentanamine as amine), workup W4. Method F, Rt: 1.03 min. m/z : 411.2
(M-H)" Exact mass: 412.1. 1H NMR (400 MHz, DMSO-d6) δ ppm 1.50-1.165 (m, 1 H), 1.81 - 2.04 (m, 3 H), 2.04 - 2.23 (m, 2 H), 2.25 (s, 3 H), 3.63 - 3.76 (m, 1 H), 7.14 (t, J=9.1 Hz, 1 H), 7.59 (dt, J=8.1, 3.9 Hz, 1 H), 7.65 - 7.72 (m, 1 H), 7.78 (t, J=7.8 Hz, 1 H), 8.02 (d, J=7.9 Hz, 1 H), 8.14 (d, J=6.8 Hz, 1 H), 8.22 (d, J=7.7 Hz, 1 H), 8.37 (s, 1 H), 10.47 (s, 1 H).
Compound 230
Figure imgf000122_0002
2-methyl-3-furoic acid (4.2 g, 32.6 mmol) was dissolved in CH2CI2 (100 mL) and cooled with an ice-bath to -5°C. Then chlorosulfonic acid (10.85 mL, 163.2 mmol) was added dropwise at a rate of 0.250 mL/min. The reaction mixture was allowed to warm to room temperature and stirred overnight. The reaction mixture was quenched on ice and extracted with 2-MeTHF. The organic layer was washed with brine, dried over MgS04 and evaporated to dryness yielding crude 5-chlorosulfonyl-2-methyl- furan-3-carboxylic acid (420 mg) as a brown oil. 5-chlorosulfonyl-2-methyl-furan-3- carboxylic acid (420 mg) was dissolved in CH2CI2 (10 mL). Hunig's base (0.64 mL, 3.74 mmol) and isopropylamine (0.478 mL, 5.61 mmol) were added and the reaction mixture was stirred overnight at room temperature. The volatiles were removed under reduced pressure and the residue was used as such in the next step. The above residue was dissolved in CH2CI2 (20 mL), 4-fluoro-3-methylaniline (228 mg, 1.82 mmol), HATU (830 mg, 2.18 mmol) and N,N-diisopropylethylamine (0.94 mL, 5.46 mmol) were added and the reaction mixture was stirred for 30 minutes. The volatiles were removed under reduced pressure and the residue was purified on silica using a heptane to EtOAc gradient resulting in compound 230 (174 mg) as a white powder. Method F, Rt: 1.00 min. m/z : 353.1 (M-H)~ Exact mass: 354.1. 1 H NMR (400 MHz, DMSO-d6) δ ppm 1.03 (d, J=6.4 Hz, 6 H), 2.23 (s, 3 H), 2.64 (s, 3 H), 3.35 - 3.43 (m, 1 H), 7.11 (t, J=9.2 Hz, 1 H), 7.53 (dd, J=7.9, 4.0 Hz, 1 H), 7.59 - 7.69 (m, 1 H), 7.72 (s, 1 H), 8.06 (d, J=5.5 Hz, 1 H), 9.87 (s, 1 H).
Compound 231
Figure imgf000123_0001
3-methyl-3-oxetanamine hydrochloride (302.6 mg, 2.45 mmol) and Hunig's base (1.15 mL, 6.68 mmol) dissolved in CH2CI2 (2 mL) were added to a solution of methyl 5-
(chlorosulfonyl)-2-furoate (thermo scientific, 500 mg, 2.23 mmol) in CH2CI2 (10 mL). The reaction mixture was stirred overnight at room temperature. The volatiles were removed under reduced pressure and the obtained residue was used as such.
The residue was dissolved in THF (10 mL). LiOH (60.2 mg, 2.514 mmol), dissolved in H20 (1 mL), was added to the reaction mixture, MeOH (1 mL) was added and this was stirred overnight at room temperature. The volatiles were removed under reduced pressure and the residue was dissolved water (25 mL). 1M HC1 (2.5 mL) was added and then 2-MeTHF (50 mL) was added. The aqueous layer was removed and the organic layer was washed with brine (50 mL). The organic layer was dried over MgSC"4, filtered and evaporated to dryness yielding an oil which was used as such in the next step. The oil and HATU (573 mg, 1.51 mmol) were stirred in CH2CI2 (5 mL) and 4-fluoro-3-methylaniline (157.3 mg,1.26 mmol) and N,N-diisopropylethylamine (0.65 mL, 3.77 mmol) were added. The reaction mixture was stirred overnight at room temperature. The volatiles were removed under reduced pressure and the residue was purified on silica using a heptane to EtOAc gradient followed by by preparative HPLC (Stationary phase: RP Vydac Denali C18 - ΙΟμιη, 200g, 5cm), Mobile phase: 0.25% NH4HCO3 solution in water, CH3CN), the desired fractions were collected, evaporated, dissolved in MeOH and evaporated again. This fraction was triturated in MeOH (4 mL), filtered and dried in the oven yielding compound 231 (305 mg) as a white solid. Method F, Rt: 0.89 min. m/z: 367.1 (M-H)~ Exact mass: 368.1. 1 H NMR (400 MHz, DMSO-dg) δ ppm 1.53 (s, 3 H), 2.24 (d, J=1.8 Hz, 3 H), 4.21 (d, J=6.6 Hz, 2 H), 4.61 (d, J=6.2 Hz, 2 H), 7.14 (t, J=9.2 Hz, 1 H), 7.26 (d, J=3.7 Hz, 1 H), 7.50 (d, J=3.7 Hz, 1 H), 7.51 - 7.57 (m, 1 H), 7.60 (dd, J=7.0, 2.4 Hz, 1 H), 8.92 (s, 1 H), 10.34 (s, 1 H). Compound 232 to 239 were prepared by slow addition of an aniline to a refluxing toluene solution of a 3-chlorosulfonylbenzoyl chloride derivative, followed by reaction with an amine in the presence of a base like NEt3 or DIPEA, as described above.
Structure Aniline Amine 3-chlorosulfonyl benzoyl chloride derivative
232 4-fluoro-3- 3-methyl-3- 2-chloro-5- methylaniline oxetanamine (chlorosulfonyl)ben zoyl chloride
233 4-fluoro-3- 3-methyl-3- 2-chloro-5- (trifluorometh oxetanamine (chlorosulfonyl)ben yl) aniline zoyl chloride
234 3,4- 3-methyl-3- 2-chloro-5- difluoroaniline oxetanamine (chlorosulfonyl)
benzoyl
chloride
235 3- 3-methyl-3- 2-chloro-5-
(difluorometh oxetanamine (chlorosulfonyl) yl)-4-fluoro- benzoyl chloride aniline
236 4-fluoro-3- (5)-3- 5-chlorosulfonyl-2- methylaniline aminotetrahydro fluoro- furan tosylate benzoyl chloride
237 4-fluoro-3- (5)-3- 2-bromo-5- methylaniline aminotetrahydro chlorosulfonyl- furan tosylate benzoyl chloride
238 4-fluoro-3- 3-methyl-3- 5-chlorosulfonyl-2- (trifluorometh oxetanamine methyl- yl) aniline benzoyl chloride Structure Aniline Amine 3-chlorosulfonyl benzoyl chloride derivative
239 4-fluoro-3- (S)- 3 -chlorosulfonyl-4- methylaniline tetrahydrofuran- fluoro- 3 -amine benzoyl chloride hydrochloride
Compound LC method Rt (min) m/z (M-H) Exact mass
232 G 1.67 410.8 412.1
233 G 1.83 464.9 466.0
234 G 1.68 414.9 416.0
235 G 1.69 446.9 448.1
236 F 0.90 395.1 396.1
237 F 0.93 457.1 458.0
238 F 1.03 445.1 446.1
239 G 1.64 394.9 396.1
Figure imgf000125_0001
Figure imgf000126_0001
Differential scanning calorimetry From 30 to 300 °C at 10°C/min: Compound 232: Peak at 169.6 °C Optical rotation:
Compound 236: [α] = - 5.83 (c 0.67 w/v %, MeOH).
Compound 240
F SOCI2 (20.1 mL, 277.2 mmol) was added slowly to water (125 mL) cooled to 5 °C, maintaining the temperature between 4 and 7 °C (addition took about 1.5 hour).
The solution was then kept stirring overnight while the temperature was allowed to slowly reach room temperature. Copper(I) chloride (76.6 mg, 0.774 mmol) was then added to the solution and it was cooled to -10 °C (dry ice/acetone bath), (resulting in solution A). In another flask cooled to 0 °C, HCl (37% in H20, 65 mL) was added dropwise to 3-amino-5-fluorobenzoic acid (10 g, 64.46 mmol), keeping the temperature below 20 °C. This slurry was cooled to -10 °C (dry ice/acetone bath) and a solution of sodium nitrite (4.803 g, 69.62 mmol) in H20 (20 mL) was added very slowly (1 drop/5 sec) to the slurry, keeping the temperature below -5°C.
After addition, the orange mixture was allowed to warm to -2 °C for 5 min before cooling back to -15 °C (solution B). Solution B was then added portionwise (plastic pipette) to solution A, cooled to -10 °C. After addition (~30 min), the reaction mixture was stirred at 0 °C for 2 h. The resulting orange solid was filtered and rinsed with water (2 x 25 mL) resulting in 3-chlorosulfonyl-5-fluoro-benzoic acid as an orange solid
(dried at 35 °C in vacuo). Et3N (1.22 mL, 8.8 mmol) was slowly added to a solution of 3-chlorosulfonyl-5-fluoro-benzoic acid (525 mg, 2.2 mmol) in dry CH2C12 (10 mL). Isopropylamine (198 μί, 2.42 mmol) was then added dropwise at room temperature to the reaction mixture.The reaction mixture was stirred at room temperature for 30 min.The brown reaction mixture was diluted with CH2C12 and water. HCl IN was added to pH 2. The layers were separated and the aqueous layer was extracted twice with CH2Cl2.The organic layer was dried on MgSC^, filtered, and evaporated resulting in 3-fluoro-5-(isopropylsulfamoyl)benzoic acid as an orange solid, which was used without further purification. HATU (356.7 mg, 0.94 mmol) was added to a solution of crude 3-fluoro-5-(isopropylsulfamoyl)benzoic acid (190 mg), 4-fluoro-3-methylaniline (78.3 mg, 0.625 mmol) and N,N-diisopropylethylamine (326.8 μί, 1.88 mmol) in CH2C12 (30 mL)at room temperature. The mixture was stirred at room temperature for 1 h. The reaction mixture was diluted with CH2C12, washed with HCl 0.5 N, filtered on Extrelut NT3 and evaporated. The obtained residue was purified by column
chromatography on silica gel (Grace Resolv 12g, eluent: CH2Cl2:MeOH 100:0 -> 95:5) resulting in compound 240 (136 mg) as a white solid, dried at 50 °C in vacuo.
Method G, Rt: 1.87 min. m/z: 366.9 (M-H)~ Exact mass: 368.1.1H NMR (360 MHz, DMSO-dg) δ ppm 0.97 (d, J=6.2 Hz, 6 H) 2.25 (d, J=1.5 Hz, 3 H) 3.30-3.39 (m, 1H), 7.16 (t, J=9.3 Hz, 1 H) 7.55 - 7.62 (m, 1 H) 7.67 (dd, J=7.1, 2.4 Hz, 1H) 7.83 (dt, J=8.0, 1.9 Hz, 1 H) 7.88 (d, J=7.0 Hz, 1 H) 8.08 (dt, J=9.3, 1.7 Hz, 1 H) 8.22 (s, 1 H) 10.52 (s, 1 H).
Compound 241
Figure imgf000128_0001
Compound 241 was prepared similarly as described for compound 240 using (S)-3- aminotetrahydrofuran tosylate instead of isopropylamine. Method G, Rt: 1.70 min. m/z: 394.9 (M-H)~ Exact mass: 396.1. 1H NMR (360 MHz, DMSO-d6) d ppm 1.55 - 1.67
(m, 1 H) 1.93 (dq, J=12.8, 7.4 Hz, 1 H) 2.25 (d, J=1.8 Hz, 3 H) 3.37 (dd, J=9.0, 4.2 Hz, 1 H) 3.55 - 3.75 (m, 3 H) 3.75 - 3.85 (m, 1 H) 7.16 (t, J=9.1 Hz, 1 H) 7.56 - 7.62 (m, 1 H) 7.67 (dd, J=7.3, 2.6 Hz, 1 H) 7.82 - 7.88 (m, 1 H) 8.08 - 8.13 (m, 1 H) 8.20 - 8.25 (m, 2 H) 10.53 (s, 1 H).
Compound 242
Figure imgf000128_0002
Compound 237 (400 mg, 0.87 mmol) was dissolved in a mixture of DMF (2.5 mL) and N-methylpyrrolidine (0.12 mL) containing Copper(I)iodide (45.43 mg, 0.24 mmol) and 2,2-difluoro-2-fluorosulfonyl acetic acid methylester (0.21 g, 1.09 mmol).
The resulting mixture was stirred at room temperature for 2 hours. An extra amount of 2,2-difluoro-2-fluorosulfonyl acetic acid methylester (0.21 g, 1.09 mmol) was added and the mixture was stirred at 60°C for 1 hour. The mixture was stirred at 60°C for 18 hours. Saturated ammonium chloride solution (10 mL) was added to the reaction mixture. Then this was extracted using EtOAc (3 x 15mL). The combined extracts were dried on Na2S04, filtered and concentrated in vacuo. The obtained residue was purified using column chromatography on silica (gradient elution: ethylacetate: heptane from 0 to 100%). All desired fractions were combined and concentrated under reduced pressure and then dried at 50°C in a vacuum oven overnight yielding compound 242 (314 mg) as a white powder. Method G, Rt: 1.73 min. m/z: 445.0 (M-H)~ Exact mass: 446.1.
Biological examples - anti-HBV activity of compounds of Formula (I)
The anti-HBV activity was measured using a stable transfected cell line,
HepG2.2.15. This cell line was described to secrete relatively consistent high levels of HBV virion particles, which have been shown to cause both acute and chronic infection and disease in chimpanzees.
For the antiviral, assay cells were treated twice for three days with serially diluted compound in 96-well plates in duplicate. After 6 days of tretament the antiviral activity was determined by quantification of purified HBV DNA from secreted virions using realtime PCR and an HBV specific primer set and probe.
Cytotoxicity of the compounds was tested in HepG2 cells using CellTiter-Blue, with the same incubation period and dose range as in the HepG2.2.15 assay. The anti HBV activity was also measured using the HepG2.117 cell line, a stable, inducibly HBV producing cell line, which replicates HBV in the absence of doxicycline (Tet-off system). For the antiviral assay, HBV replication was induced, followed by a treatment with serially diluted compound in 96-well plates in duplicate. After 3 days of treatment, the antiviral activity was determined by quantification of intracellular HBV DNA using realtime PCR and an HBV specific primer set and probe.
Cytotoxicity of the compounds was tested using HepG2 cells, incubated for 4 days in the presence of compounds. The viability of the cells was assessed using a Resazurin assay. Results are displayed in Table 1.
Table 1.
Figure imgf000129_0001
Figure imgf000130_0001
Figure imgf000131_0001
Figure imgf000132_0001
Figure imgf000133_0001
Figure imgf000134_0001
Figure imgf000135_0001
Figure imgf000136_0001
Figure imgf000137_0001
Figure imgf000138_0001
-138-
Figure imgf000139_0001
Figure imgf000140_0001
Figure imgf000141_0001
Figure imgf000142_0001
Figure imgf000143_0001
Figure imgf000144_0001
Figure imgf000145_0001
Figure imgf000146_0001
Figure imgf000147_0001
Figure imgf000148_0001
Figure imgf000149_0001
Figure imgf000150_0001
Figure imgf000151_0001
Figure imgf000152_0001
Figure imgf000153_0001
Figure imgf000154_0001
Figure imgf000155_0001
Figure imgf000156_0001
Figure imgf000157_0001
Figure imgf000158_0001
Figure imgf000159_0001
Figure imgf000160_0001
Figure imgf000161_0001
Figure imgf000162_0001
Figure imgf000163_0001
Figure imgf000164_0001
Figure imgf000165_0001
Figure imgf000166_0001
Figure imgf000167_0001
Figure imgf000168_0001
Figure imgf000169_0001
Figure imgf000170_0001
-170-
Figure imgf000171_0001
Figure imgf000172_0001
Figure imgf000173_0001

Claims

Claims
1. A compound of Formula (la)
Figure imgf000174_0001
or a stereoisomer or tautomeric form thereof, wherein:
B represents a monocyclic 5 to 6 membered aromatic ring, optionally containing one or more heteroatoms each independently selected from the group consisting of O, S and N, such 5 to 6 membered aromatic ring optionally being substituted with one or more substituents each independently selected from the group consisting of hydrogen, halo, Ci-C3alkyl, CN, CFH2, CF2H and CF3;
Ri represents hydrogen or Ci-C3alkyl; R2 represents Ci-C6alkyl, Ci-C3alkyl-R5, benzyl, C(=0)-R5, CFH2, CF2H, CF3 or a 3-7 membered saturated ring optionally containing one or more heteroatoms each independently selected from the group consisting of O, S and N, such 3-7 membered saturated ring or Ci-Cealkyl optionally being substituted with one or more substituents each independently selected from the group consisting of hydrogen, halo, Ci-C4alkyloxy, oxo, C(=0)-Ci-C3alkyl, Ci-C4alkyl, OH, CN,
CFH2, CF2H and CF3;
Or Ri R2 together with the Nitrogen to which they are attached form a 1 ,4-dioxa- 8-azaspiro[4.5] moiety or a 5-7 membered saturated ring, optionally containing one or more additional heteroatoms each independently selected from the group consisting of O, S and N, such 5-7 membered saturated ring optionally being substituted with one or more substituents each independently selected from the group consisting of hydrogen, halo, Ci-C4alkyloxy, oxo C(=0)-Ci-C3alkyl, Ci-C4alkyl, OH, CN, CFH2, CF2H and CF3;
Each R4 is independently selected from hydrogen, halo, Ci-C4alkyloxy, Ci-C4alkyl, OH, CN, CFH2, CF2H, CF3 or a 3-5 membered saturated ring optionally containing one or more heteroatoms each independently selected from the group consisting of O and N;
R5 represents Ci-Cealkyl, CFH2, CF2H, CF3 or a 3-7 membered saturated ring
optionally containing one or more heteroatoms each independently selected from the group consisting of O, S and N, such 3-7 membered saturated ring optionally being substituted with one or more substituents each independently selected from the group consisting of hydrogen, halo, Ci-C4alkyloxy, oxo,
Figure imgf000175_0001
Ci-C4alkyl, OH, CN, CFH2, CF2H and CF3; or a pharmaceutically acceptable salt or a solvate thereof.
2. The compound according to claim 1 , wherein R2 represents a 3-7 membered
saturated ring, containing one or more heteroatoms each independently selected from the group consisting of O, S and N, such 3-7 membered saturated ring optionally being substituted with one or more substituents each independently selected from the group consisting of hydrogen, halo, Ci-C4alkyloxy, C(=0)- Ci- C3alkyl, Ci-C4alkyl, OH, CN, CFH2, CF2H and CF3; Or Ri R2 together with the Nitrogen to which they are attached form a 5-7 membered saturated ring, optionally containing one or more additional heteroatoms each independently selected from the group consisting of O, S and N, such 5-7 membered saturated ring optionally being substituted with one or more substituents each independently selected from the group consisting of hydrogen, halo,
Ci C4alkyloxy, oxo, C(=0)-Ci-C3alkyl, Ci-C4alkyl, OH, CN, CFH2, CF2H and CF3.
3. The compound according to claim 1 or 2, wherein R2 represents a 4-7 membered saturated ring containing carbon and one or more oxygen atoms, such 4-7 membered saturated ring optionally being substituted with one or more substituents each independently selected from the group consisting of hydrogen, halo,
Ci C4alkyloxy, C(=0)- Ci-C3alkyl, Ci-C4alkyl, OH, CN, CFH2, CF2H and CF3.
4. A compound according any one of claims 1 to 3, wherein B represents phenyl or thiophene, optionally being substituted with one or more substituents each independently selected from the group consisting of hydrogen, halogen, Ci-C3alkyl,
CN, CFH2, CF2H and CF3.
5. A compound of Formula (I) according to any one of the previous claims, wherein R2 represents Ci-C3alkyl-R6 or a 4-7 membered saturated ring consisting of carbon atoms and one or more heteroatoms each independently selected from the group consisting of O or S, such 4-7 membered saturated ring optionally being substituted with one or more substituents each independently selected from the group consisting of hydrogen, halo, Ci-C4alkyloxy, oxo,
Figure imgf000176_0001
Ci-C4alkyl,
OH, CN, CFH2, CF2H and CF3;
Each R4 is independently selected from hydrogen, halo, Ci-C4alkyloxy, Ci-C4alkyl, OH, CN, CFH2, CF2H, CF3 or a 3-5 membered saturated ring optionally containing one or more heteroatoms each independently selected from the group consisting of O and N; and
Re represents a 4-7 membered saturated ring optionally containing one or more
heteroatoms each independently selected from the group consisting of O or S, such 4-7 membered saturated ring optionally being substituted with one or more substituents each independently selected from the group consisting of hydrogen, halo, Ci-C4alkyloxy, oxo,
Figure imgf000176_0002
Ci-C4alkyl, OH, CN, CFH2, CF2H and CF3.
A compound according to any one of the previous claims, which is of Formula (lb)
Figure imgf000176_0003
(lb) wherein Rl s R2, R4 are defined as in any one of the previous claims and R3 is selected from the group comprising hydrogen, halo, Ci-C3alkyl, CN, CFH2, CF2H, CF3.
7. A compound according to any one of the previous claims, wherein at least one R4 represents Fluor, Ci-C3alkyl or cyclopropyl.
8. A compound according to any one of the previous claims, wherein one R4 on the para position represents Fluor and the other one R4 on the meta position represents methyl and such compound is not
Figure imgf000177_0001
9. A compound according to any one of the previous claims, wherein R3 represents Fluor.
10. A compound according to any one of claims 1 to 9, wherein B represents phenyl or thiophene, optionally being substituted with one or more substituents each independently selected from the group consisting of hydrogen, halogen, Ci-C3alkyl, CN, CFH2, CF2H and CF3.
1 1. A compound according to any one of the previous claims for use in the prevention or treatment of an HBV infection in a mammal.
12. A pharmaceutical composition comprising a compound according to any of claims 1 to 10, and a pharmaceutically acceptable carrier.
13. A product containing (a) a compound of formula I as defined in any one of claims 1 to 10, and (b) another HBV inhibitor, as a combined preparation for simultaneous, separate or sequential use in the treatment of HBV infections.
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