CA2618218C - N-(arylamino)-sulfonamide inhibitors of mek - Google Patents
N-(arylamino)-sulfonamide inhibitors of mek Download PDFInfo
- Publication number
- CA2618218C CA2618218C CA2618218A CA2618218A CA2618218C CA 2618218 C CA2618218 C CA 2618218C CA 2618218 A CA2618218 A CA 2618218A CA 2618218 A CA2618218 A CA 2618218A CA 2618218 C CA2618218 C CA 2618218C
- Authority
- CA
- Canada
- Prior art keywords
- compound
- phenyl
- fluoro
- methyl
- alkyl
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
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- 239000003112 inhibitor Substances 0.000 title abstract description 7
- 229940124530 sulfonamide Drugs 0.000 title description 26
- 239000000460 chlorine Substances 0.000 claims description 320
- -1 cyanomethyl Chemical group 0.000 claims description 206
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 188
- 150000001875 compounds Chemical class 0.000 claims description 170
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 119
- 229910052731 fluorine Inorganic materials 0.000 claims description 81
- 229910052739 hydrogen Inorganic materials 0.000 claims description 75
- 229910052801 chlorine Inorganic materials 0.000 claims description 70
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 48
- 229910052794 bromium Inorganic materials 0.000 claims description 42
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 42
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 41
- 229910052740 iodine Inorganic materials 0.000 claims description 40
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 39
- 239000000203 mixture Substances 0.000 claims description 34
- 125000000217 alkyl group Chemical group 0.000 claims description 32
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims description 30
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 claims description 22
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 22
- 125000003545 alkoxy group Chemical group 0.000 claims description 19
- 229910052736 halogen Inorganic materials 0.000 claims description 19
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 19
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims description 17
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 17
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 16
- 150000002367 halogens Chemical class 0.000 claims description 16
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 claims description 15
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 14
- 125000005843 halogen group Chemical group 0.000 claims description 14
- 125000001424 substituent group Chemical group 0.000 claims description 14
- 229910052799 carbon Inorganic materials 0.000 claims description 11
- VUWZPRWSIVNGKG-UHFFFAOYSA-N fluoromethane Chemical compound F[CH2] VUWZPRWSIVNGKG-UHFFFAOYSA-N 0.000 claims description 11
- 150000003839 salts Chemical class 0.000 claims description 11
- 229940124647 MEK inhibitor Drugs 0.000 claims description 10
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims description 10
- 125000003226 pyrazolyl group Chemical group 0.000 claims description 10
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims description 9
- 125000003342 alkenyl group Chemical group 0.000 claims description 9
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 8
- 150000002148 esters Chemical class 0.000 claims description 8
- 125000001153 fluoro group Chemical group F* 0.000 claims description 8
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 8
- 229910052757 nitrogen Inorganic materials 0.000 claims description 8
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 8
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 claims description 7
- QOXOZONBQWIKDA-UHFFFAOYSA-N 3-hydroxypropyl Chemical group [CH2]CCO QOXOZONBQWIKDA-UHFFFAOYSA-N 0.000 claims description 7
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 7
- 125000000304 alkynyl group Chemical group 0.000 claims description 7
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims description 6
- 102100031480 Dual specificity mitogen-activated protein kinase kinase 1 Human genes 0.000 claims description 6
- 101710146526 Dual specificity mitogen-activated protein kinase kinase 1 Proteins 0.000 claims description 6
- JNCMHMUGTWEVOZ-UHFFFAOYSA-N F[CH]F Chemical compound F[CH]F JNCMHMUGTWEVOZ-UHFFFAOYSA-N 0.000 claims description 6
- 108010081348 HRT1 protein Hairy Proteins 0.000 claims description 6
- 102100021881 Hairy/enhancer-of-split related with YRPW motif protein 1 Human genes 0.000 claims description 6
- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims description 6
- 125000004786 difluoromethoxy group Chemical group [H]C(F)(F)O* 0.000 claims description 6
- 239000003937 drug carrier Substances 0.000 claims description 6
- 125000004785 fluoromethoxy group Chemical group [H]C([H])(F)O* 0.000 claims description 6
- 125000004170 methylsulfonyl group Chemical group [H]C([H])([H])S(*)(=O)=O 0.000 claims description 6
- 229920006395 saturated elastomer Polymers 0.000 claims description 6
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims description 5
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 5
- 125000000131 cyclopropyloxy group Chemical group C1(CC1)O* 0.000 claims description 5
- 125000004076 pyridyl group Chemical group 0.000 claims description 5
- 125000004509 1,3,4-oxadiazol-2-yl group Chemical group O1C(=NN=C1)* 0.000 claims description 4
- 102100023266 Dual specificity mitogen-activated protein kinase kinase 2 Human genes 0.000 claims description 4
- 101710146529 Dual specificity mitogen-activated protein kinase kinase 2 Proteins 0.000 claims description 4
- 150000001721 carbon Chemical group 0.000 claims description 4
- 125000005842 heteroatom Chemical group 0.000 claims description 4
- 239000008194 pharmaceutical composition Substances 0.000 claims description 4
- 229910052717 sulfur Inorganic materials 0.000 claims description 4
- MBIZXFATKUQOOA-UHFFFAOYSA-N 1,3,4-thiadiazole Chemical compound C1=NN=CS1 MBIZXFATKUQOOA-UHFFFAOYSA-N 0.000 claims description 3
- 125000000094 2-phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 claims description 3
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 claims description 3
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 3
- 125000004356 hydroxy functional group Chemical group O* 0.000 claims description 3
- ZMSIFDIKIXVLDF-UHFFFAOYSA-N 2-methyl-1,3,4-oxadiazole Chemical compound CC1=NN=CO1 ZMSIFDIKIXVLDF-UHFFFAOYSA-N 0.000 claims description 2
- 125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 claims description 2
- 125000004216 fluoromethyl group Chemical group [H]C([H])(F)* 0.000 claims description 2
- 230000005764 inhibitory process Effects 0.000 claims description 2
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 2
- RDSACQWTXKSHJT-NSHDSACASA-N n-[3,4-difluoro-2-(2-fluoro-4-iodoanilino)-6-methoxyphenyl]-1-[(2s)-2,3-dihydroxypropyl]cyclopropane-1-sulfonamide Chemical compound C1CC1(C[C@H](O)CO)S(=O)(=O)NC=1C(OC)=CC(F)=C(F)C=1NC1=CC=C(I)C=C1F RDSACQWTXKSHJT-NSHDSACASA-N 0.000 claims 1
- 229910052760 oxygen Inorganic materials 0.000 claims 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract description 5
- 206010028980 Neoplasm Diseases 0.000 abstract description 4
- 201000011510 cancer Diseases 0.000 abstract description 3
- 201000010099 disease Diseases 0.000 abstract description 3
- 230000003463 hyperproliferative effect Effects 0.000 abstract description 3
- 125000004421 aryl sulphonamide group Chemical group 0.000 abstract description 2
- 239000000243 solution Substances 0.000 description 79
- 101150041968 CDC13 gene Proteins 0.000 description 76
- HEDRZPFGACZZDS-MICDWDOJSA-N Trichloro(2H)methane Chemical compound [2H]C(Cl)(Cl)Cl HEDRZPFGACZZDS-MICDWDOJSA-N 0.000 description 76
- 238000000034 method Methods 0.000 description 66
- 238000005160 1H NMR spectroscopy Methods 0.000 description 65
- 239000000047 product Substances 0.000 description 57
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 56
- 239000011541 reaction mixture Substances 0.000 description 43
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 41
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 38
- SAWNQHAMLZSIMQ-UHFFFAOYSA-N 3,4-difluoro-2-n-(2-fluoro-4-iodophenyl)benzene-1,2-diamine Chemical compound NC1=CC=C(F)C(F)=C1NC1=CC=C(I)C=C1F SAWNQHAMLZSIMQ-UHFFFAOYSA-N 0.000 description 32
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 30
- 238000006243 chemical reaction Methods 0.000 description 30
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 28
- 235000019341 magnesium sulphate Nutrition 0.000 description 28
- CBOIHMRHGLHBPB-UHFFFAOYSA-N hydroxymethyl Chemical compound O[CH2] CBOIHMRHGLHBPB-UHFFFAOYSA-N 0.000 description 25
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 22
- 238000003756 stirring Methods 0.000 description 20
- YBBRCQOCSYXUOC-UHFFFAOYSA-N sulfuryl dichloride Chemical class ClS(Cl)(=O)=O YBBRCQOCSYXUOC-UHFFFAOYSA-N 0.000 description 20
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 19
- 239000002904 solvent Substances 0.000 description 19
- 239000012043 crude product Substances 0.000 description 18
- 238000000746 purification Methods 0.000 description 18
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- 102000004232 Mitogen-Activated Protein Kinase Kinases Human genes 0.000 description 17
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 17
- 238000005481 NMR spectroscopy Methods 0.000 description 15
- 239000012267 brine Substances 0.000 description 15
- 238000010898 silica gel chromatography Methods 0.000 description 15
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 15
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 14
- 239000012044 organic layer Substances 0.000 description 14
- 239000007787 solid Substances 0.000 description 14
- 239000003039 volatile agent Substances 0.000 description 14
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- 102000043136 MAP kinase family Human genes 0.000 description 12
- 108091054455 MAP kinase family Proteins 0.000 description 12
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 12
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 12
- 229910052938 sodium sulfate Inorganic materials 0.000 description 12
- 235000011152 sodium sulphate Nutrition 0.000 description 12
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 11
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 10
- WMSPXQIQBQAWLL-UHFFFAOYSA-N cyclopropanesulfonamide Chemical compound NS(=O)(=O)C1CC1 WMSPXQIQBQAWLL-UHFFFAOYSA-N 0.000 description 10
- 230000000694 effects Effects 0.000 description 10
- 102000016914 ras Proteins Human genes 0.000 description 10
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- 239000012074 organic phase Substances 0.000 description 9
- 239000000725 suspension Substances 0.000 description 9
- BQZRYUOIXPREMR-RLWSFTDUSA-N (4R,4aR,7aR,12bS)-9-methoxy-3-methyl-1,2,4,4a,5,6,7a,13-octahydro-4,12-methanobenzofuro[3,2-e]isoquinolin-7-one N,N-dimethyl-1-phenothiazin-10-ylpropan-2-amine N-(4-hydroxyphenyl)acetamide Chemical compound CC(=O)NC1=CC=C(O)C=C1.C1=CC=C2N(CC(C)N(C)C)C3=CC=CC=C3SC2=C1.C([C@H]1[C@H](N(CC[C@@]112)C)C3)CC(=O)[C@@H]1OC1=C2C3=CC=C1OC BQZRYUOIXPREMR-RLWSFTDUSA-N 0.000 description 8
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 8
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- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 8
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- AQYNREAFYINZPS-UHFFFAOYSA-N 1-prop-2-enylcyclopropane-1-sulfonyl chloride Chemical compound C=CCC1(S(=O)(=O)Cl)CC1 AQYNREAFYINZPS-UHFFFAOYSA-N 0.000 description 7
- 125000002941 2-furyl group Chemical group O1C([*])=C([H])C([H])=C1[H] 0.000 description 7
- XKMLYUALXHKNFT-UUOKFMHZSA-N Guanosine-5'-triphosphate Chemical compound C1=2NC(N)=NC(=O)C=2N=CN1[C@@H]1O[C@H](COP(O)(=O)OP(O)(=O)OP(O)(O)=O)[C@@H](O)[C@H]1O XKMLYUALXHKNFT-UUOKFMHZSA-N 0.000 description 7
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- YNESATAKKCNGOF-UHFFFAOYSA-N lithium bis(trimethylsilyl)amide Chemical compound [Li+].C[Si](C)(C)[N-][Si](C)(C)C YNESATAKKCNGOF-UHFFFAOYSA-N 0.000 description 7
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- 210000004027 cell Anatomy 0.000 description 6
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- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 5
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- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 4
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- NEAQRZUHTPSBBM-UHFFFAOYSA-N 2-hydroxy-3,3-dimethyl-7-nitro-4h-isoquinolin-1-one Chemical compound C1=C([N+]([O-])=O)C=C2C(=O)N(O)C(C)(C)CC2=C1 NEAQRZUHTPSBBM-UHFFFAOYSA-N 0.000 description 3
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- AFVFQIVMOAPDHO-UHFFFAOYSA-M methanesulfonate group Chemical class CS(=O)(=O)[O-] AFVFQIVMOAPDHO-UHFFFAOYSA-M 0.000 description 1
- AJDKPDGQECETSC-UHFFFAOYSA-N methyl 3-[[3,4-difluoro-2-(2-fluoro-4-iodoanilino)phenyl]sulfamoyl]thiophene-2-carboxylate Chemical compound S1C=CC(S(=O)(=O)NC=2C(=C(F)C(F)=CC=2)NC=2C(=CC(I)=CC=2)F)=C1C(=O)OC AJDKPDGQECETSC-UHFFFAOYSA-N 0.000 description 1
- PJVJBDAUWILEOG-UHFFFAOYSA-N methyl 3-chlorosulfonylthiophene-2-carboxylate Chemical compound COC(=O)C=1SC=CC=1S(Cl)(=O)=O PJVJBDAUWILEOG-UHFFFAOYSA-N 0.000 description 1
- QPJVMBTYPHYUOC-UHFFFAOYSA-N methyl benzoate Chemical class COC(=O)C1=CC=CC=C1 QPJVMBTYPHYUOC-UHFFFAOYSA-N 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 201000006417 multiple sclerosis Diseases 0.000 description 1
- YSVNJRJKOSRWLI-UHFFFAOYSA-N n-[2-(2,4-dichloroanilino)-3,4-difluorophenyl]cyclopropanesulfonamide Chemical compound C=1C=C(Cl)C=C(Cl)C=1NC1=C(F)C(F)=CC=C1NS(=O)(=O)C1CC1 YSVNJRJKOSRWLI-UHFFFAOYSA-N 0.000 description 1
- IKSNKNDSWYHLPH-UHFFFAOYSA-N n-[2-(4-chloro-2-fluoroanilino)-3,4-difluorophenyl]cyclopropanesulfonamide Chemical compound C=1C=C(Cl)C=C(F)C=1NC1=C(F)C(F)=CC=C1NS(=O)(=O)C1CC1 IKSNKNDSWYHLPH-UHFFFAOYSA-N 0.000 description 1
- CMLJEMBUAYQSHE-UHFFFAOYSA-N n-[2-(4-tert-butyl-2-chloroanilino)-3,4-difluorophenyl]cyclopropanesulfonamide Chemical compound ClC1=CC(C(C)(C)C)=CC=C1NC1=C(F)C(F)=CC=C1NS(=O)(=O)C1CC1 CMLJEMBUAYQSHE-UHFFFAOYSA-N 0.000 description 1
- JDKJCGUGODIUCP-UHFFFAOYSA-N n-[3,4,6-trifluoro-2-(2-fluoro-4-iodoanilino)phenyl]cyclopropanesulfonamide Chemical compound C=1C=C(I)C=C(F)C=1NC1=C(F)C(F)=CC(F)=C1NS(=O)(=O)C1CC1 JDKJCGUGODIUCP-UHFFFAOYSA-N 0.000 description 1
- GAOTVJNSYXCSHT-UHFFFAOYSA-N n-[3,4-difluoro-2-(2-fluoro-4-iodoanilino)-6-methoxyphenyl]-1-prop-2-enylcyclopropane-1-sulfonamide Chemical compound C1CC1(CC=C)S(=O)(=O)NC=1C(OC)=CC(F)=C(F)C=1NC1=CC=C(I)C=C1F GAOTVJNSYXCSHT-UHFFFAOYSA-N 0.000 description 1
- XNAGWHHRYVZGCW-UHFFFAOYSA-N n-[3,4-difluoro-2-(2-fluoro-4-iodoanilino)-6-methoxyphenyl]cyclopropanesulfonamide Chemical compound C1CC1S(=O)(=O)NC=1C(OC)=CC(F)=C(F)C=1NC1=CC=C(I)C=C1F XNAGWHHRYVZGCW-UHFFFAOYSA-N 0.000 description 1
- KSWCSEXYKHVUHP-UHFFFAOYSA-N n-[3,4-difluoro-2-(2-fluoro-4-iodoanilino)phenyl]benzenesulfonamide Chemical compound C=1C=C(I)C=C(F)C=1NC1=C(F)C(F)=CC=C1NS(=O)(=O)C1=CC=CC=C1 KSWCSEXYKHVUHP-UHFFFAOYSA-N 0.000 description 1
- FPPMHVSDXJYUKL-UHFFFAOYSA-N n-[3,4-difluoro-2-(2-fluoro-4-iodoanilino)phenyl]butane-1-sulfonamide Chemical compound CCCCS(=O)(=O)NC1=CC=C(F)C(F)=C1NC1=CC=C(I)C=C1F FPPMHVSDXJYUKL-UHFFFAOYSA-N 0.000 description 1
- CORRTDDVKPNIRC-UHFFFAOYSA-N n-[3,4-difluoro-2-(2-fluoro-4-iodoanilino)phenyl]butane-2-sulfonamide Chemical compound CCC(C)S(=O)(=O)NC1=CC=C(F)C(F)=C1NC1=CC=C(I)C=C1F CORRTDDVKPNIRC-UHFFFAOYSA-N 0.000 description 1
- QVFCQVIAXHDDAM-UHFFFAOYSA-N n-[3,4-difluoro-2-(2-fluoro-4-iodoanilino)phenyl]cyclohexanesulfonamide Chemical compound C=1C=C(I)C=C(F)C=1NC1=C(F)C(F)=CC=C1NS(=O)(=O)C1CCCCC1 QVFCQVIAXHDDAM-UHFFFAOYSA-N 0.000 description 1
- XPONOSPNILDOOQ-UHFFFAOYSA-N n-[3,4-difluoro-2-(2-fluoro-4-iodoanilino)phenyl]cyclopentanesulfonamide Chemical compound C=1C=C(I)C=C(F)C=1NC1=C(F)C(F)=CC=C1NS(=O)(=O)C1CCCC1 XPONOSPNILDOOQ-UHFFFAOYSA-N 0.000 description 1
- XDGYXPPEVYEFTJ-UHFFFAOYSA-N n-[3,4-difluoro-2-(2-fluoro-4-iodoanilino)phenyl]furan-2-sulfonamide Chemical compound C=1C=C(I)C=C(F)C=1NC1=C(F)C(F)=CC=C1NS(=O)(=O)C1=CC=CO1 XDGYXPPEVYEFTJ-UHFFFAOYSA-N 0.000 description 1
- OJEFRCWRZRAHAS-UHFFFAOYSA-N n-[3,4-difluoro-2-(2-fluoro-4-iodoanilino)phenyl]propane-2-sulfonamide Chemical compound CC(C)S(=O)(=O)NC1=CC=C(F)C(F)=C1NC1=CC=C(I)C=C1F OJEFRCWRZRAHAS-UHFFFAOYSA-N 0.000 description 1
- VQLUFKCIQCLFPG-UHFFFAOYSA-N n-[3,4-difluoro-2-(2-fluoro-4-iodoanilino)phenyl]thiophene-3-sulfonamide Chemical compound C=1C=C(I)C=C(F)C=1NC1=C(F)C(F)=CC=C1NS(=O)(=O)C=1C=CSC=1 VQLUFKCIQCLFPG-UHFFFAOYSA-N 0.000 description 1
- XJOADFGFTJCTOD-UHFFFAOYSA-N n-[3,4-difluoro-2-(4-iodo-2-methylanilino)phenyl]cyclopropanesulfonamide Chemical compound CC1=CC(I)=CC=C1NC1=C(F)C(F)=CC=C1NS(=O)(=O)C1CC1 XJOADFGFTJCTOD-UHFFFAOYSA-N 0.000 description 1
- PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical class C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 1
- KVBGVZZKJNLNJU-UHFFFAOYSA-N naphthalene-2-sulfonic acid Chemical class C1=CC=CC2=CC(S(=O)(=O)O)=CC=C21 KVBGVZZKJNLNJU-UHFFFAOYSA-N 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 150000002828 nitro derivatives Chemical class 0.000 description 1
- LQNUZADURLCDLV-UHFFFAOYSA-N nitrobenzene Substances [O-][N+](=O)C1=CC=CC=C1 LQNUZADURLCDLV-UHFFFAOYSA-N 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 230000000414 obstructive effect Effects 0.000 description 1
- WWZKQHOCKIZLMA-UHFFFAOYSA-M octanoate Chemical class CCCCCCCC([O-])=O WWZKQHOCKIZLMA-UHFFFAOYSA-M 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 150000007530 organic bases Chemical class 0.000 description 1
- 201000008482 osteoarthritis Diseases 0.000 description 1
- 150000003901 oxalic acid esters Chemical class 0.000 description 1
- 125000000160 oxazolidinyl group Chemical group 0.000 description 1
- 239000000546 pharmaceutical excipient Substances 0.000 description 1
- DYUMLJSJISTVPV-UHFFFAOYSA-N phenyl propanoate Chemical class CCC(=O)OC1=CC=CC=C1 DYUMLJSJISTVPV-UHFFFAOYSA-N 0.000 description 1
- WLJVXDMOQOGPHL-UHFFFAOYSA-N phenylacetic acid Chemical class OC(=O)CC1=CC=CC=C1 WLJVXDMOQOGPHL-UHFFFAOYSA-N 0.000 description 1
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 230000000865 phosphorylative effect Effects 0.000 description 1
- 125000005498 phthalate group Chemical class 0.000 description 1
- 230000004962 physiological condition Effects 0.000 description 1
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- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 1
- 235000015320 potassium carbonate Nutrition 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 238000011533 pre-incubation Methods 0.000 description 1
- 238000002953 preparative HPLC Methods 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 108090000765 processed proteins & peptides Chemical group 0.000 description 1
- 102000004196 processed proteins & peptides Human genes 0.000 description 1
- 230000035755 proliferation Effects 0.000 description 1
- VVWRJUBEIPHGQF-UHFFFAOYSA-N propan-2-yl n-propan-2-yloxycarbonyliminocarbamate Chemical compound CC(C)OC(=O)N=NC(=O)OC(C)C VVWRJUBEIPHGQF-UHFFFAOYSA-N 0.000 description 1
- KCXFHTAICRTXLI-UHFFFAOYSA-N propane-1-sulfonic acid Chemical class CCCS(O)(=O)=O KCXFHTAICRTXLI-UHFFFAOYSA-N 0.000 description 1
- DRINJBFRTLBHNF-UHFFFAOYSA-N propane-2-sulfonyl chloride Chemical compound CC(C)S(Cl)(=O)=O DRINJBFRTLBHNF-UHFFFAOYSA-N 0.000 description 1
- UORVCLMRJXCDCP-UHFFFAOYSA-N propynoic acid Chemical class OC(=O)C#C UORVCLMRJXCDCP-UHFFFAOYSA-N 0.000 description 1
- 150000003246 quinazolines Chemical class 0.000 description 1
- 102000009929 raf Kinases Human genes 0.000 description 1
- 108010077182 raf Kinases Proteins 0.000 description 1
- 102000027426 receptor tyrosine kinases Human genes 0.000 description 1
- 108091008598 receptor tyrosine kinases Proteins 0.000 description 1
- 102000005962 receptors Human genes 0.000 description 1
- 108020003175 receptors Proteins 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 206010039073 rheumatoid arthritis Diseases 0.000 description 1
- YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical class OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 1
- 238000007423 screening assay Methods 0.000 description 1
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical class OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 1
- 150000003335 secondary amines Chemical class 0.000 description 1
- 125000003607 serino group Chemical group [H]N([H])[C@]([H])(C(=O)[*])C(O[H])([H])[H] 0.000 description 1
- 230000019491 signal transduction Effects 0.000 description 1
- 230000011664 signaling Effects 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 239000012279 sodium borohydride Substances 0.000 description 1
- 229910000033 sodium borohydride Inorganic materials 0.000 description 1
- 239000012312 sodium hydride Substances 0.000 description 1
- 229910000104 sodium hydride Inorganic materials 0.000 description 1
- 239000012453 solvate Substances 0.000 description 1
- 238000003797 solvolysis reaction Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- TYFQFVWCELRYAO-UHFFFAOYSA-N suberic acid Chemical class OC(=O)CCCCCCC(O)=O TYFQFVWCELRYAO-UHFFFAOYSA-N 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 150000003900 succinic acid esters Chemical class 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical class [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 1
- 150000003871 sulfonates Chemical class 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 239000006228 supernatant Substances 0.000 description 1
- 150000003899 tartaric acid esters Chemical class 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- 238000002560 therapeutic procedure Methods 0.000 description 1
- 125000001984 thiazolidinyl group Chemical group 0.000 description 1
- YSPWSQNKRBSICH-UHFFFAOYSA-N thiophene-3-sulfonyl chloride Chemical compound ClS(=O)(=O)C=1C=CSC=1 YSPWSQNKRBSICH-UHFFFAOYSA-N 0.000 description 1
- 230000009466 transformation Effects 0.000 description 1
- 150000003852 triazoles Chemical class 0.000 description 1
- RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical compound C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 0.000 description 1
- 238000007514 turning Methods 0.000 description 1
- OUYCCCASQSFEME-UHFFFAOYSA-N tyrosine Natural products OC(=O)C(N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-UHFFFAOYSA-N 0.000 description 1
- 238000011144 upstream manufacturing Methods 0.000 description 1
- 239000013598 vector Substances 0.000 description 1
- GDJZZWYLFXAGFH-UHFFFAOYSA-M xylenesulfonate group Chemical group C1(C(C=CC=C1)C)(C)S(=O)(=O)[O-] GDJZZWYLFXAGFH-UHFFFAOYSA-M 0.000 description 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
- C07D307/34—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D307/56—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D307/64—Sulfur atoms
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
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- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
- C07C311/01—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms
- C07C311/02—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton
- C07C311/08—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton having the nitrogen atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
- C07C311/01—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms
- C07C311/02—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton
- C07C311/09—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton the carbon skeleton being further substituted by at least two halogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
- C07C311/01—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms
- C07C311/10—Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of a saturated carbon skeleton containing rings
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
- C07C311/14—Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of rings other than six-membered aromatic rings
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
- C07C311/15—Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings
- C07C311/21—Sulfonamides having sulfur atoms of sulfonamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
- C07C311/22—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound oxygen atoms
- C07C311/28—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound oxygen atoms having the sulfur atom of at least one of the sulfonamide groups bound to a carbon atom of a ring other than a six-membered aromatic ring
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- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
- C07C311/22—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound oxygen atoms
- C07C311/29—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound oxygen atoms 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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- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/30—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members
- C07D207/34—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D207/36—Oxygen or sulfur atoms
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- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D231/18—One oxygen or sulfur atom
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- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
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- C07D233/66—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D233/84—Sulfur atoms
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D261/00—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings
- C07D261/02—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings
- C07D261/06—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members
- C07D261/10—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
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- C07D277/32—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
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- C07D277/32—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D277/54—Nitrogen and either oxygen or sulfur atoms
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Abstract
This invention concerns N-(2-arylamino) aryl sulfonamides of formula I:
(see formula I) which are inhibitors of MEK and might therefore be potentially useful in treatment of cancer and other hyperproliferative diseases.
(see formula I) which are inhibitors of MEK and might therefore be potentially useful in treatment of cancer and other hyperproliferative diseases.
Description
N-(ARYLAMINO) SULFONAMIDE INHIBITORS OF HEX
Field of the Invention This invention concerns N-(2-arylamino) aryl sulfonamides, which are inhibitors of MEK. Such compounds might therefore be potentially useful in the treatment of cancer and other hyperproliferative diseases.
Background of the invention Oncogenes -- genes that contribute to the production of cancers -- are generally mutated forms of certain normal cellular genes ("proto-oncogenes"). Oncogenes often encode abnormal versions of signal pathway components, such as receptor tyrosine kinases, serine-threonine kinases, or downstream signaling molecules. The central downstream signaling molecules are the Ras proteins, which are anchored on the inner surfaces of cytoplasmic membranes, and which hydrolyze bound guanosine triphosphate (GTP) to guanosine diphosphate (GDP). When activated by a growth factor, growth factor receptors initiate a chain of reactions that leads to the activation of guanine nucleotide exchange activity on Ras. Ras alternates between an active "on" state with a bound GTP
(hereafter "Ras.GTP") and an inactive "off" state with a bound GDP. The active "on"
state, Ras.GTP, binds to and activates proteins that control the growth and differentiation of cells.
For example, in the "mitogen-activatedprotein kinase (MAP kinase) cascade,"
Ras,GTP leads to the activation of a cascade of serine/threonine kinases. One of several groups of kinases known to require a Ras.GTP for their own activation is the Raf family. The Raf proteins activate "MEK1" and "MEIC2," abbreviations for mitogen-activated ERK-activating kinases (where ERK is extracellular signakegulated protein kinase, another designation for MAPK). MEK1 and MEK2 are dual-function serine/threonine and tyrosine protein kinases and are also known as MAP kinase kinases. Thus, Ras.GTP
activates Raf, which activates MEK1 and MEK2, which activate MAP kinase (MAPK). Activation of MAP
kinase by mitogens appears to be essential for proliferation, and constitutive activation of this kinase is sufficient to induce cellular transformation. Blockade of downstream Ras signaling, as by use of a dominant negative Raf-1 protein, can completely inhibit mitogenesis, whether induced from cell surface receptors or from oncogenic Ras mutants.
The interaction of Raf and Ras is a key regulatory step in the control of cell proliferation. To date, no substrates of MEK other than MAPK have been identified;
however, recent reports indicate that MEK may also be activated by other upstream signal proteins such as MEK kinase or MEKK1 and PKC. Activated MAPK translocates and accumulates in the nucleus, where it can phosphorylate and activate transcription factors such as Elk-1 and Sapl a, leading to the enhanced expression of genes such as that for c-fos.
Once activated, Raf and other kinases phosphorylate MEK on two neighboring serine residues, S218 and S222 in the case of MEK-1. These phosphorylations are required for activation of MEK as a kinase. In turn, MEK phosphorylates MAP kinase on two residues separated by a single amino acid: a tyrosine, Y185 and a threonine, T183. MEK
appears to associate strongly with MAP kinase prior to phosphorylating it, suggesting that phosphorylation of MAP kinase by MEK may require a prior strong interaction between the two proteins. Two factors ¨ MEK's unusual specificity and its requirement for a strong interaction with MAP kinase prior to phosphorylation -- suggest that MEK's mechanism of action may differ sufficiently from the mechanisms of other protein kinases as to allow for selective inhibitors of MEK. Possibly, such inhibitors would operate through allosteric mechanisms rather than through the more usual mechanism involving blockage of an ATP
binding site.
Thus, MEK1 and MEK2 are validated and accepted targets for anti-proliferative therapies, even when the oncogenic mutation does not affect MEK structure or expression.
See, e.g., U.S. Patent Publications 2003/0149015 by Barrett et al. and 2004/0029898 by Boyle et al.
Field of the Invention This invention concerns N-(2-arylamino) aryl sulfonamides, which are inhibitors of MEK. Such compounds might therefore be potentially useful in the treatment of cancer and other hyperproliferative diseases.
Background of the invention Oncogenes -- genes that contribute to the production of cancers -- are generally mutated forms of certain normal cellular genes ("proto-oncogenes"). Oncogenes often encode abnormal versions of signal pathway components, such as receptor tyrosine kinases, serine-threonine kinases, or downstream signaling molecules. The central downstream signaling molecules are the Ras proteins, which are anchored on the inner surfaces of cytoplasmic membranes, and which hydrolyze bound guanosine triphosphate (GTP) to guanosine diphosphate (GDP). When activated by a growth factor, growth factor receptors initiate a chain of reactions that leads to the activation of guanine nucleotide exchange activity on Ras. Ras alternates between an active "on" state with a bound GTP
(hereafter "Ras.GTP") and an inactive "off" state with a bound GDP. The active "on"
state, Ras.GTP, binds to and activates proteins that control the growth and differentiation of cells.
For example, in the "mitogen-activatedprotein kinase (MAP kinase) cascade,"
Ras,GTP leads to the activation of a cascade of serine/threonine kinases. One of several groups of kinases known to require a Ras.GTP for their own activation is the Raf family. The Raf proteins activate "MEK1" and "MEIC2," abbreviations for mitogen-activated ERK-activating kinases (where ERK is extracellular signakegulated protein kinase, another designation for MAPK). MEK1 and MEK2 are dual-function serine/threonine and tyrosine protein kinases and are also known as MAP kinase kinases. Thus, Ras.GTP
activates Raf, which activates MEK1 and MEK2, which activate MAP kinase (MAPK). Activation of MAP
kinase by mitogens appears to be essential for proliferation, and constitutive activation of this kinase is sufficient to induce cellular transformation. Blockade of downstream Ras signaling, as by use of a dominant negative Raf-1 protein, can completely inhibit mitogenesis, whether induced from cell surface receptors or from oncogenic Ras mutants.
The interaction of Raf and Ras is a key regulatory step in the control of cell proliferation. To date, no substrates of MEK other than MAPK have been identified;
however, recent reports indicate that MEK may also be activated by other upstream signal proteins such as MEK kinase or MEKK1 and PKC. Activated MAPK translocates and accumulates in the nucleus, where it can phosphorylate and activate transcription factors such as Elk-1 and Sapl a, leading to the enhanced expression of genes such as that for c-fos.
Once activated, Raf and other kinases phosphorylate MEK on two neighboring serine residues, S218 and S222 in the case of MEK-1. These phosphorylations are required for activation of MEK as a kinase. In turn, MEK phosphorylates MAP kinase on two residues separated by a single amino acid: a tyrosine, Y185 and a threonine, T183. MEK
appears to associate strongly with MAP kinase prior to phosphorylating it, suggesting that phosphorylation of MAP kinase by MEK may require a prior strong interaction between the two proteins. Two factors ¨ MEK's unusual specificity and its requirement for a strong interaction with MAP kinase prior to phosphorylation -- suggest that MEK's mechanism of action may differ sufficiently from the mechanisms of other protein kinases as to allow for selective inhibitors of MEK. Possibly, such inhibitors would operate through allosteric mechanisms rather than through the more usual mechanism involving blockage of an ATP
binding site.
Thus, MEK1 and MEK2 are validated and accepted targets for anti-proliferative therapies, even when the oncogenic mutation does not affect MEK structure or expression.
See, e.g., U.S. Patent Publications 2003/0149015 by Barrett et al. and 2004/0029898 by Boyle et al.
2 Several examples of 1-substituted-2(p-substituted-phenylamino)-aryl inhibitors of MEK have been reported. U.S. Patent Nos. 6,440,966 and 6,750,217 and corresponding publication WO 00/42003 described carboxylic and hydroxamic acid esters and N-substituted amide derivatives of sulfonamide-substituted-2(4-iodophenylamino)-benzoic acid esters and N-substituted benzamides as functioning as MEK inhibitors. The sulfonamide may also be N-substituted.
U.S. Patent 6,545,030 and corresponding publication WO 00/42029 describe MEK
inhibitors that are 1-heterocycly1-2(4-iodophenylamino)-benzene, where the heterocycle is a five-membered nitrogen-containing ring such as pyrazole, triazole, oxazole, isoxazole, and isoxazolinone. The more recent U.S. Patent Publication 2005/004186 describes related compounds in which the 4-iodo substituent of the '030 patent is replaced by a very broad genus of moieties including alkyl, alkoxy, acyloxy, alkenyl, carbamoyl, carbamoylalkyl, carboxyl, carboxylalkyl, N-acylsulfonamido, and others.
U.S. Patent 6,469,004 and corresponding publication WO 00/42022 describe carboxylic and hydroxamic acid esters of a group of heterocyclo-condensed phenylene compounds, i.e., benzimidazoles, benzooxazoles, benzothiazoles, benzothiadiazoles, quinazolines, etc.. The heterocycles are 7-F-6-(4-iodo-phenylamino)-5-carboxylic acid esters, carboxylic acid amides or hydroxamic acid esters. More recent publication U.S.
2005/0026970 described similar compounds in which the 4-iodo substituent was replaced by a very broad genus of structures. Related compounds are described in patent publications WO 03/077855, WO 03/77914 and US 2005/0554701. Further examples of 2-(4-iodophenylamino)-phenylhydroxamic acid esters which are reported to be useful as MEK
inhibitors can be found in WO 2005/028426.
Patent Publication WO 02/06213 and corresponding U.S. Application Ser. No.
10/333,399 (U.S. 2004/0054172) describe hydroxy-substituted acid esters of 1-oxamic acid-2(4-halophenylamino)-3,4-difluorobenzene. U.S. Patent No. 6,891,066 and corresponding publication WO 03/62191 describe similar compounds wherein the 4-halo substituent is replaced by a very broad genus of structures. Among the substituents in the 4-position were methyl, ethyl, ethynyl, and 2-hydroxyethyl. Specific related compounds are described in U.S.
Patent No. 6,770,778.
U.S. Patent 6,545,030 and corresponding publication WO 00/42029 describe MEK
inhibitors that are 1-heterocycly1-2(4-iodophenylamino)-benzene, where the heterocycle is a five-membered nitrogen-containing ring such as pyrazole, triazole, oxazole, isoxazole, and isoxazolinone. The more recent U.S. Patent Publication 2005/004186 describes related compounds in which the 4-iodo substituent of the '030 patent is replaced by a very broad genus of moieties including alkyl, alkoxy, acyloxy, alkenyl, carbamoyl, carbamoylalkyl, carboxyl, carboxylalkyl, N-acylsulfonamido, and others.
U.S. Patent 6,469,004 and corresponding publication WO 00/42022 describe carboxylic and hydroxamic acid esters of a group of heterocyclo-condensed phenylene compounds, i.e., benzimidazoles, benzooxazoles, benzothiazoles, benzothiadiazoles, quinazolines, etc.. The heterocycles are 7-F-6-(4-iodo-phenylamino)-5-carboxylic acid esters, carboxylic acid amides or hydroxamic acid esters. More recent publication U.S.
2005/0026970 described similar compounds in which the 4-iodo substituent was replaced by a very broad genus of structures. Related compounds are described in patent publications WO 03/077855, WO 03/77914 and US 2005/0554701. Further examples of 2-(4-iodophenylamino)-phenylhydroxamic acid esters which are reported to be useful as MEK
inhibitors can be found in WO 2005/028426.
Patent Publication WO 02/06213 and corresponding U.S. Application Ser. No.
10/333,399 (U.S. 2004/0054172) describe hydroxy-substituted acid esters of 1-oxamic acid-2(4-halophenylamino)-3,4-difluorobenzene. U.S. Patent No. 6,891,066 and corresponding publication WO 03/62191 describe similar compounds wherein the 4-halo substituent is replaced by a very broad genus of structures. Among the substituents in the 4-position were methyl, ethyl, ethynyl, and 2-hydroxyethyl. Specific related compounds are described in U.S.
Patent No. 6,770,778.
3 =
Patent Publication WO 04/083167, published September 30, 2004, (in Japanese) discloses more than two thousand ¨ but provides NMR data for only 400 ¨ 1-(N-substituted sulfonyl urea)-2(2,4-dihalophenylamino)-3,4-difluorobenzenes and asserts that they useful as MEK inhibitors. Data indicating inhibition of MEK were presented for a subgroup of just twelve. In addition to a secondary or tertiary amine, these twelve compounds all contained one of the following groups: an N, N-disubstituted sulfonyl urea, N-piperazinesulfonamide, N-piperidinesulfonamide or N-pyrrolidinesulfonamide.
The MEK cascade has also been implicated in inflammatory diseases and disorders.
U.S. Application Publication No. 2006/0030610 to Koch et ?I., U.S. Application Publication No. 2006/0140872 to Fume et at. This includes both acute and chronic inflammation disorders. Examples of such disorders are allergic contact dermatitis, rheumatoid arthritis, osteoarthritis, inflammatory bowel diseases, chronic obstructive pulmonary disorder, psoriasis, multiple sclerosis, asthma, diseases and disorders related to diabetic complications, and inflammatory complications of the cardiovascular system such as acute coronary syndrome. Among inflammatory bowel diseases are Crohn's disease and ulcerative colitis.
Brief Description of the Invention This invention provides compounds of formula I
Qi Ro NH *
F ' =
where G is Rh, Rib) Rio, Rid, Rio, Ari, Ar2or Ar3; R is H, halogen, C1-C6 alkyl, CI-C4 alkoxy, C3-C6 cycloalkyl, C2-C6 alkenyl, C2-C6 alicynyl, said alkyl, cycloalkyl, alkenyl, and allcynyl groups optionally substituted with 1-3 substituents selected independently from halogen, OH, CN, cyanomethyl, nitro, phenyl, and trifluoromethyl, and said C1-C6 alkyl and C1-C4 alkoxy groups also optionally substituted with OCH3 or OCH2CH3; X is F, Cl or
Patent Publication WO 04/083167, published September 30, 2004, (in Japanese) discloses more than two thousand ¨ but provides NMR data for only 400 ¨ 1-(N-substituted sulfonyl urea)-2(2,4-dihalophenylamino)-3,4-difluorobenzenes and asserts that they useful as MEK inhibitors. Data indicating inhibition of MEK were presented for a subgroup of just twelve. In addition to a secondary or tertiary amine, these twelve compounds all contained one of the following groups: an N, N-disubstituted sulfonyl urea, N-piperazinesulfonamide, N-piperidinesulfonamide or N-pyrrolidinesulfonamide.
The MEK cascade has also been implicated in inflammatory diseases and disorders.
U.S. Application Publication No. 2006/0030610 to Koch et ?I., U.S. Application Publication No. 2006/0140872 to Fume et at. This includes both acute and chronic inflammation disorders. Examples of such disorders are allergic contact dermatitis, rheumatoid arthritis, osteoarthritis, inflammatory bowel diseases, chronic obstructive pulmonary disorder, psoriasis, multiple sclerosis, asthma, diseases and disorders related to diabetic complications, and inflammatory complications of the cardiovascular system such as acute coronary syndrome. Among inflammatory bowel diseases are Crohn's disease and ulcerative colitis.
Brief Description of the Invention This invention provides compounds of formula I
Qi Ro NH *
F ' =
where G is Rh, Rib) Rio, Rid, Rio, Ari, Ar2or Ar3; R is H, halogen, C1-C6 alkyl, CI-C4 alkoxy, C3-C6 cycloalkyl, C2-C6 alkenyl, C2-C6 alicynyl, said alkyl, cycloalkyl, alkenyl, and allcynyl groups optionally substituted with 1-3 substituents selected independently from halogen, OH, CN, cyanomethyl, nitro, phenyl, and trifluoromethyl, and said C1-C6 alkyl and C1-C4 alkoxy groups also optionally substituted with OCH3 or OCH2CH3; X is F, Cl or
4 methyl; Y is I, Br, Cl, CF3, C1-C3 alkyl, C2-C3 alkenyl, C2-C3 alkynyl, cyclopropyl, phenyl, PYridY1, Pyrazolyl, OMe, OEt, or SMe, where all said methyl, ethyl, C1-C3 alkyl, and cyclopropyl groups of X and Y are optionally substituted with OH, all said phenyl, pyridyl, pyrazolyl groups of Y are optionally substituted with halogen, acetyl, methyl, and trifluoromethyl, and all said methyl groups of X and Y are optionally substituted with one, two, or three F atoms; and Z is H or F, where RI a is methyl, optionally substituted with 1-3 fluorine atoms or 1-3 chlorine atoms, or with OH, cyclopropoxy, or Ci- C4 alkoxy, where the CI- C4 alkyl moieties of said Cl- C4 alkoxy groups are optionally substituted with one hydroxy or methoxy group, and where all C2- C4 alkyl groups within said Ci- C4 alkoxy are optionally further substituted with a second OH group;
Rib is CH(CH3)-C1_3 alkyl or C3-C6 cycloalkyl, said methyl, alkyl, and cycloalkyl groups optionally substituted with 1-3 substituents selected independently from F, Cl, Br, I, OH, C1-C4 alkoxy, and CN;
Ric is (CH2)nOna', where m is 0 or 1; where, when m is 1, n is 2 or 3, and when m is 0, n is 1 or 2; and where R' is C1-C6 alkyl, optionally substituted with 1-3 substituents selected independently from F, Cl, OH, OCH3, OCH2CH3, and C3-C6 cycloalkyl;
Rid is C(A)(A')(B)- where B, A, and A' are, independently, H or Ci4 alkyl, optionally substituted with one or two OH groups or halogen atoms, or A and A', together with the carbon atom to which they are attached, form a 3- to 6- member saturated ring, said ring optionally containing one or two heteroatoms selected, independently, from 0, N, and S and optionally substituted with one or two groups selected independently from methyl, ethyl, and halo;
Ric is benzyl or 2-phenyl ethyl, in which the phenyl group is optionally substituted R2,6N (CI-12)q-i --/
a
Rib is CH(CH3)-C1_3 alkyl or C3-C6 cycloalkyl, said methyl, alkyl, and cycloalkyl groups optionally substituted with 1-3 substituents selected independently from F, Cl, Br, I, OH, C1-C4 alkoxy, and CN;
Ric is (CH2)nOna', where m is 0 or 1; where, when m is 1, n is 2 or 3, and when m is 0, n is 1 or 2; and where R' is C1-C6 alkyl, optionally substituted with 1-3 substituents selected independently from F, Cl, OH, OCH3, OCH2CH3, and C3-C6 cycloalkyl;
Rid is C(A)(A')(B)- where B, A, and A' are, independently, H or Ci4 alkyl, optionally substituted with one or two OH groups or halogen atoms, or A and A', together with the carbon atom to which they are attached, form a 3- to 6- member saturated ring, said ring optionally containing one or two heteroatoms selected, independently, from 0, N, and S and optionally substituted with one or two groups selected independently from methyl, ethyl, and halo;
Ric is benzyl or 2-phenyl ethyl, in which the phenyl group is optionally substituted R2,6N (CI-12)q-i --/
a
5 where q is 1 or 2, R2, R3 and R4 are, independently, H, F, Cl, Br, CH3, CH2F, CHF2, CF3, OCH3, OCH2F, OCHF2, OCF3, ethyl, n-propyl, isopropyl, cyclopropyl, isobutyl, sec-butyl, tert-butyl, and methylsulfonyl, and R4 may also be nitro, acetamido, amidinyl, cyano, carbamoyl, methylcarbamoyl, dimethylcarbamoyl, 1,3,4-oxadiazol-2-yl, 5-methyl-1,3,4-oxadiazolyl, 1,3,4-thiadiazolyl, 5-methyl-1,3,4-thiadiazol-/H-tetrazolyl, N-morpholinyl carbonylamino, N-morpholinylsulfonyl, and N-pyrrolidinylcarbonylarnino; R5 and Rg are, independently, H, F, Cl, or methyl;
Ari is where U and V are, independently, N, CR2 or CR3; R2, R3 and R4 are, independently, H, F, Cl, Br, CH3, CH2F, CHF2, CF3, OCH3, OCH2F, OCHF2, OCF3, ethyl, n-propyl, isopropyl, cyclopropyl, isobutyl, sec-butyl, tert-butyl, and methylsulfonyl, and R4 may also be nitro, acetamido, amidinyl, cyano, carbamoyl, methylcarbamoyl, dimethylcarbamoyl, 1,3,4-oxadiazol-2-yl, 5-methyl-1,3,4-oxadiazol, 1,3,4-thiadiazol, 5-methyl-1,3,4-thiadiazol 1H-tetrazolyl, N-morpholinylcarbonylamino, N-morpholinylsulfonyl and N-pyrrolidinylcarbonylamino; R5 and Rg are, independently, H, F, Cl or methyl;
Ar2 is Ar2 where the dashed line represents a double bond which may be located formally either between V and the carbon between U and V, or between U and the carbon between U and V;
where U is -S-, -0- or ¨N = and where, when U is -0- or -S-, V is -CH=, -CC1=
or -N =; and when U is -N =, V CH=, or -NCH3-; R7 and R8 are, independently, H, methoxycarbonyl, methylcarbamoyl, acetamido, acetyl, methyl, ethyl, trifluoromethyl, or halogen.
Ar3 is
Ari is where U and V are, independently, N, CR2 or CR3; R2, R3 and R4 are, independently, H, F, Cl, Br, CH3, CH2F, CHF2, CF3, OCH3, OCH2F, OCHF2, OCF3, ethyl, n-propyl, isopropyl, cyclopropyl, isobutyl, sec-butyl, tert-butyl, and methylsulfonyl, and R4 may also be nitro, acetamido, amidinyl, cyano, carbamoyl, methylcarbamoyl, dimethylcarbamoyl, 1,3,4-oxadiazol-2-yl, 5-methyl-1,3,4-oxadiazol, 1,3,4-thiadiazol, 5-methyl-1,3,4-thiadiazol 1H-tetrazolyl, N-morpholinylcarbonylamino, N-morpholinylsulfonyl and N-pyrrolidinylcarbonylamino; R5 and Rg are, independently, H, F, Cl or methyl;
Ar2 is Ar2 where the dashed line represents a double bond which may be located formally either between V and the carbon between U and V, or between U and the carbon between U and V;
where U is -S-, -0- or ¨N = and where, when U is -0- or -S-, V is -CH=, -CC1=
or -N =; and when U is -N =, V CH=, or -NCH3-; R7 and R8 are, independently, H, methoxycarbonyl, methylcarbamoyl, acetamido, acetyl, methyl, ethyl, trifluoromethyl, or halogen.
Ar3 is
6 Ar3 where U is -NH-, -NCH3- or -0-; and R7 and R8 are, independently, H, F, Cl, or methyl.
Such compounds are inhibitors of MEK and might therefore be potentially useful in treatment of cancer and other hyperproliferative diseases.
This invention is also directed to pharmaceutical compositions comprising pharmaceutically effective amounts of a compound of formula I or a pharmaceutically acceptable salt, ester, prodrug, solvate, or hydrate thereof, and a pharmaceutically acceptable carrier. Such compositions may contain adjuvants, excipients, preservatives, agents for delaying absorption, fillers, binders, adsorbents, buffers, disintegrating agents, solubilizing agents, other carriers, and other inert ingredients. Methods of formulation of such compositions are well-known in the art. If the composition comprises a specific isomer, then the composition may be substantially free of the other isomer.
Embodiments of the present invention include: a compound of formula I
//
N'NH X
Ro NH
where G is RI, Rib, Rlo Rid, orRie; R is H, halogen, CH3NH-, (CH3)2N-, C1-C6 alkyl, Ci-C4 alkoxy, C3-C6 cycloalkyl, C2-C6 alkenyl, C2-C6 alkynyl, said alkyl, alkoxy, cycloalkyl, alkenyl, and alkynyl groups optionally substituted with 1-3 substituents selected
Such compounds are inhibitors of MEK and might therefore be potentially useful in treatment of cancer and other hyperproliferative diseases.
This invention is also directed to pharmaceutical compositions comprising pharmaceutically effective amounts of a compound of formula I or a pharmaceutically acceptable salt, ester, prodrug, solvate, or hydrate thereof, and a pharmaceutically acceptable carrier. Such compositions may contain adjuvants, excipients, preservatives, agents for delaying absorption, fillers, binders, adsorbents, buffers, disintegrating agents, solubilizing agents, other carriers, and other inert ingredients. Methods of formulation of such compositions are well-known in the art. If the composition comprises a specific isomer, then the composition may be substantially free of the other isomer.
Embodiments of the present invention include: a compound of formula I
//
N'NH X
Ro NH
where G is RI, Rib, Rlo Rid, orRie; R is H, halogen, CH3NH-, (CH3)2N-, C1-C6 alkyl, Ci-C4 alkoxy, C3-C6 cycloalkyl, C2-C6 alkenyl, C2-C6 alkynyl, said alkyl, alkoxy, cycloalkyl, alkenyl, and alkynyl groups optionally substituted with 1-3 substituents selected
7 independently from the group consisting of halogen, OH, CN, cyanomethyl, nitro, phenyl, and trifluoromethyl, and said C1-C6 alkyl and CI-CI alkoxy groups also optionally substituted with OCH3 or OCH2CH3; X is F, Cl, or methyl; Y is I, Br, Cl, CF3, C1-C3 alkyl, C2-C3 alkenyl, C2-C3 alkynyl, cyclopropyl, phenyl, pyridyl, pyrazolyl, OMe, OEt, or SMe, where all said methyl, ethyl, C1-C3 alkyl, and cyclopropyl groups of X and Y are optionally substituted with OH, where all said phenyl, pyridyl, pyrazolyl groups of Y are optionally substituted with halogen, acetyl, methyl, or trifluoromethyl, and where all said methyl groups of X and Y are optionally substituted with one, two, or three F atoms; and Z is H or F;
where Ria is methyl, optionally substituted with 1-3 fluorine atoms or 1-3 chlorine atoms, or with OH, cyclopropoxy, or Ci-C4 alkoxy, where said cyclopropoxy group or the CI-CI alkyl moieties of said CI-C.4 alkoxy groups are optionally substituted with one hydroxy or methoxy group, and where all C2-C4 alkyl groups within said CI-C.4 alkoxy are optionally further substituted with a second OH group;
Rib is CH(CH3)-C1.3 alkyl or C3-C6 cycloalkyl, said methyl, alkyl and cycloalkyl groups optionally substituted with 1-3 substituents selected independently from F, Cl, Br, I, OH, OCH3, and CN;
R1c is (CH2),,O,õR', where m is 0 or 1; where, when m is I, n is 2 or 3, and when m is 0, n is 1 or 2; and where R' is CI-C6 alkyl, optionally substituted with 1-3 substituents selected independently from F, Cl, OH, OCH3, OCH2CH3, and C3-C6 cycloalkyl;
Rid is C(A)(A')(B)- where B, A, and A' are, independently, H or Ci_4alkyl, optionally substituted with one or two OH groups or halogen atoms, or A and A', together with the carbon atom to which they are attached, form a 3- to 6- member saturated ring, said ring optionally containing one or two heteroatoms selected, independently, from 0, N, and S and optionally substituted with one or two groups selected independently from methyl, ethyl, and halo; and RI e is benzyl or 2-phenyl ethyl, in which the phenyl group is optionally substituted, as shown below:
7a 0, R2-6,......, "....... (CH2)q¨
N
../e.
Rie where q is 1 or 2, R2, R3 and R.4 are, independently, H, F, Cl, Br, CH3, CH2F, CHF2, CF3, OCH3, OCH2F, OCHF2, OCF3, ethyl, n-propyl, isopropyl, cyclopropyl, isobutyl, sec-butyl, tert-butyl, or methylsulfonyl, and R4 may also be nitro, acetamido, amidinyl, cyano, carbamoyl, methylcarbamoyl, dimethylcarbamoyl, 1,3,4-oxadiazol-2-yl, 5-methy1-1,3,4-oxadiazol, 1,3,4-thiadiazol, 5-methyl-1,3,4-thiadiazol 1H-tetrazolyl, N-morpholyl carbonyl amino, N-morpholylsulfonyl or N-pyrrolidinylcarbonylamino; R5 and R6 are independently H, F, Cl or methyl.
Further embodiments of the compounds defined by formula I include those where one or more of the following definitions may apply:
= X is F, Cl, or CH3: Y is I, Br, Cl, CF3, or C1-C3 alkyl; and Z is H or F;
= R is F, Cl, CI-CI alkyl or C1-C4 alkoxy, said CI-CI alkyl group and the C1-C4 alkyl moiety of said CI-C.4 alkoxy group optionally substituted with F, Cl, OCH3, or OCH2CH3;
= R is H, F, Cl, CI-C.4 alkyl, methoxy, ethoxy, or 2-methoxy-ethoxy; and optionally G is Ria and Z is F;
= G is CH3; R is H; Z is F; and Y is Br, I, CF3, or CH3;
= G is Rib;
= G is Rib and Z is F; and optionally le is H, F, or OCH3, X is F or CH3, and Y is Br, I, or CH3;
= G is unsubstituted C3-C6 cycloalkyl; and optionally R is H; and/or G is isopropyl or cyclopropyl;
7b = G is Ric;
= G is R1e, Y is I, Br, CH3, or CF3; and Z is F; and optionally m is zero;
= G is Rid;
= G is Rid; R is fluoro, chloro, methyl, ethyl, propyl, isopropyl, sec-butyl, iso-butyl, tert-butyl, cyclopropyl, cyclobutyl, fluoromethyl, methoxy, fluoromethoxy, methylamino or dimethylamino; X is F, Cl, CH3, or mono-, di- or tri-fluoromethyl; Y is I, Br, Cl, or mono-, di- or tri- fluoromethyl; and Z is H or F;
= G is Rid; R is F, Cl, methyl, ethyl, methoxy, ethoxy, or 2-methoxy-ethoxy;
X is F, Cl, or CH3; Y is I, Br, Cl, or mono-, di- or tri- fluoromethyl; and Z
is H or F;
= G is Rid; R is H; X is F, Cl, CH3, or mono-, di- or tri- fluoromethyl; Y is I, Br, Cl, or mono-, di- or tri- fluoromethyl; and Z is H or F;
= C(A)(A') is C3-C6 cycloalkyl, such as cyclopropyl; and B is H; or B is methyl, optionally substituted with one OH group, or C2-C4 alkyl, optionally substituted with one or two OH groups; or B is methyl, ethyl, 2-hydroxyethyl, n-propyl, 3-hydroxypropyl, 2,3-dihydroxypropyl, 3,4-dihydroxybutyl, isopropyl, 1-methy1-2-hydroxy ethyl, n-butyl, sec-butyl, isobutyl, or 2-hydroxymethy1-3-hydroxy propyl; or B is 2,3-dihydroxypropyl or 3,4-dihydroxybutyl; and optionally, a chiral carbon in B is in the R
configuration; and = G is Rie; and optionally q is 1; R is H, R.4_6 are H; R2 and R3 are, independently, H, F, Cl, Br, CH3, CH2F, CHF2, CF3, OCH3, OCH2F, OCHF2, OCF3, ethyl, n-propyl, isopropyl, cyclopropyl, isobutyl, sec-butyl, tert-butyl, or methylsulfonyl; X is F and Y is I.
7c In one subgeneric embodiment, this invention provides a compound of formula IA-1, X
NH
where Ria is defined as above.
In another embodiment the invention provides a compound of formula IA-2, where Ria is defined as above and where R ' is R , defined above, other than H.
Re NH
In another embodiment, the invention provides a compound of formula IB-1, NH
where X and Y are defined as for formula I, and where Rib is defined as above for formula I.
In another embodiment, the invention provides a compound of formula IB-2,
where Ria is methyl, optionally substituted with 1-3 fluorine atoms or 1-3 chlorine atoms, or with OH, cyclopropoxy, or Ci-C4 alkoxy, where said cyclopropoxy group or the CI-CI alkyl moieties of said CI-C.4 alkoxy groups are optionally substituted with one hydroxy or methoxy group, and where all C2-C4 alkyl groups within said CI-C.4 alkoxy are optionally further substituted with a second OH group;
Rib is CH(CH3)-C1.3 alkyl or C3-C6 cycloalkyl, said methyl, alkyl and cycloalkyl groups optionally substituted with 1-3 substituents selected independently from F, Cl, Br, I, OH, OCH3, and CN;
R1c is (CH2),,O,õR', where m is 0 or 1; where, when m is I, n is 2 or 3, and when m is 0, n is 1 or 2; and where R' is CI-C6 alkyl, optionally substituted with 1-3 substituents selected independently from F, Cl, OH, OCH3, OCH2CH3, and C3-C6 cycloalkyl;
Rid is C(A)(A')(B)- where B, A, and A' are, independently, H or Ci_4alkyl, optionally substituted with one or two OH groups or halogen atoms, or A and A', together with the carbon atom to which they are attached, form a 3- to 6- member saturated ring, said ring optionally containing one or two heteroatoms selected, independently, from 0, N, and S and optionally substituted with one or two groups selected independently from methyl, ethyl, and halo; and RI e is benzyl or 2-phenyl ethyl, in which the phenyl group is optionally substituted, as shown below:
7a 0, R2-6,......, "....... (CH2)q¨
N
../e.
Rie where q is 1 or 2, R2, R3 and R.4 are, independently, H, F, Cl, Br, CH3, CH2F, CHF2, CF3, OCH3, OCH2F, OCHF2, OCF3, ethyl, n-propyl, isopropyl, cyclopropyl, isobutyl, sec-butyl, tert-butyl, or methylsulfonyl, and R4 may also be nitro, acetamido, amidinyl, cyano, carbamoyl, methylcarbamoyl, dimethylcarbamoyl, 1,3,4-oxadiazol-2-yl, 5-methy1-1,3,4-oxadiazol, 1,3,4-thiadiazol, 5-methyl-1,3,4-thiadiazol 1H-tetrazolyl, N-morpholyl carbonyl amino, N-morpholylsulfonyl or N-pyrrolidinylcarbonylamino; R5 and R6 are independently H, F, Cl or methyl.
Further embodiments of the compounds defined by formula I include those where one or more of the following definitions may apply:
= X is F, Cl, or CH3: Y is I, Br, Cl, CF3, or C1-C3 alkyl; and Z is H or F;
= R is F, Cl, CI-CI alkyl or C1-C4 alkoxy, said CI-CI alkyl group and the C1-C4 alkyl moiety of said CI-C.4 alkoxy group optionally substituted with F, Cl, OCH3, or OCH2CH3;
= R is H, F, Cl, CI-C.4 alkyl, methoxy, ethoxy, or 2-methoxy-ethoxy; and optionally G is Ria and Z is F;
= G is CH3; R is H; Z is F; and Y is Br, I, CF3, or CH3;
= G is Rib;
= G is Rib and Z is F; and optionally le is H, F, or OCH3, X is F or CH3, and Y is Br, I, or CH3;
= G is unsubstituted C3-C6 cycloalkyl; and optionally R is H; and/or G is isopropyl or cyclopropyl;
7b = G is Ric;
= G is R1e, Y is I, Br, CH3, or CF3; and Z is F; and optionally m is zero;
= G is Rid;
= G is Rid; R is fluoro, chloro, methyl, ethyl, propyl, isopropyl, sec-butyl, iso-butyl, tert-butyl, cyclopropyl, cyclobutyl, fluoromethyl, methoxy, fluoromethoxy, methylamino or dimethylamino; X is F, Cl, CH3, or mono-, di- or tri-fluoromethyl; Y is I, Br, Cl, or mono-, di- or tri- fluoromethyl; and Z is H or F;
= G is Rid; R is F, Cl, methyl, ethyl, methoxy, ethoxy, or 2-methoxy-ethoxy;
X is F, Cl, or CH3; Y is I, Br, Cl, or mono-, di- or tri- fluoromethyl; and Z
is H or F;
= G is Rid; R is H; X is F, Cl, CH3, or mono-, di- or tri- fluoromethyl; Y is I, Br, Cl, or mono-, di- or tri- fluoromethyl; and Z is H or F;
= C(A)(A') is C3-C6 cycloalkyl, such as cyclopropyl; and B is H; or B is methyl, optionally substituted with one OH group, or C2-C4 alkyl, optionally substituted with one or two OH groups; or B is methyl, ethyl, 2-hydroxyethyl, n-propyl, 3-hydroxypropyl, 2,3-dihydroxypropyl, 3,4-dihydroxybutyl, isopropyl, 1-methy1-2-hydroxy ethyl, n-butyl, sec-butyl, isobutyl, or 2-hydroxymethy1-3-hydroxy propyl; or B is 2,3-dihydroxypropyl or 3,4-dihydroxybutyl; and optionally, a chiral carbon in B is in the R
configuration; and = G is Rie; and optionally q is 1; R is H, R.4_6 are H; R2 and R3 are, independently, H, F, Cl, Br, CH3, CH2F, CHF2, CF3, OCH3, OCH2F, OCHF2, OCF3, ethyl, n-propyl, isopropyl, cyclopropyl, isobutyl, sec-butyl, tert-butyl, or methylsulfonyl; X is F and Y is I.
7c In one subgeneric embodiment, this invention provides a compound of formula IA-1, X
NH
where Ria is defined as above.
In another embodiment the invention provides a compound of formula IA-2, where Ria is defined as above and where R ' is R , defined above, other than H.
Re NH
In another embodiment, the invention provides a compound of formula IB-1, NH
where X and Y are defined as for formula I, and where Rib is defined as above for formula I.
In another embodiment, the invention provides a compound of formula IB-2,
8 /,0 NH X
Ro' õI NH =
where Rib is defined as above for formula I, and where R ' is R , defined above, other than H.
In a third embodiment, this invention provides a compound of formula IC-1, NH
where Ric is (CH2)nOmIZI, where m is 0 or 1, n is 2 or 3 when m is 1, and n is 1 or 2 when m is 0, and R' is C1-C6 alkyl, optionally substituted with 1-3 substituents selected independently from F, Cl, OH, OCH3, OCH2CH3, and C3-C6 cycloalkyl.
In another embodiment, this invention provides a compound of formula IC-2, Rd NH
=
where R10 is defined as above and where R ' is R , defined above, other than H.
In another embodiment, this invention provides a compound of formula ID-1
Ro' õI NH =
where Rib is defined as above for formula I, and where R ' is R , defined above, other than H.
In a third embodiment, this invention provides a compound of formula IC-1, NH
where Ric is (CH2)nOmIZI, where m is 0 or 1, n is 2 or 3 when m is 1, and n is 1 or 2 when m is 0, and R' is C1-C6 alkyl, optionally substituted with 1-3 substituents selected independently from F, Cl, OH, OCH3, OCH2CH3, and C3-C6 cycloalkyl.
In another embodiment, this invention provides a compound of formula IC-2, Rd NH
=
where R10 is defined as above and where R ' is R , defined above, other than H.
In another embodiment, this invention provides a compound of formula ID-1
9 Ftick // N X
NH
where Rid is C(A)(A')(B)- where B, A, and A' are, independently, H or C1-4 alkyl, optionally substituted with one or two OH groups or halogen atoms, or A and A', together with the carbon atom to which they are attached, form a 3- to 6- member saturated ring, said ring optionally containing one or two heteroatoms selected, independently, from 0, N, and S and optionally substituted with one or two groups selected independently from methyl, ethyl, and halo In another embodiment, the invention provides a compound of formula ID-2, Rlet //0 // N X
Ro' NH
where Rid is defined as above and where R ' is R , defined above, other than H.
In another embodiment, this invention provides a compound of formula IE-1.
,0 // N X
where Rie is defined as above.
In another embodiment, this invention provides a compound of formula 1E-2, R1 e Ro' 00 NH
where R ' is R , defined above, other than H.
In another embodiment, this invention provides a compound of formula II-A, where G.
is An, NH
II-A
where R2-6, U, and V are defined as above.
In another embodiment, this invention provides a compound of formula II-B, SN
II-B
where R ' is R , defined above, other than H.
In another embodiment, this invention provides a compound of formula III-A
..V/R7-8 li---Z-st."¨S/
//N
Z Y
F
III-A
In another embodiment, this invention provides a compound of formula 111-13 R7_8 erV/S/ 0 - / h Ul--....177-----gf //N
Z Y
F
III-B
where R ' is R , defined above, other than H.
In additional subgeneric embodiments, this invention provides compounds of formulas IA-1, IA-2, 1B-1, I13-2, IC-1, IC-2, ID-1, ID2, II-A, II-B, III-A, and III-B, where X
is F, Cl, or CH3: Y is I, Br, Cl, CF3, or C1-C3 alkyl, and Z is H or F.
In additional subgeneric embodiments, this invention provides compounds of formulas IA-2, IB-2, IC-2, ID-2, II-B, and III-B, where X is F, Cl, or CH3: Y
is I, Br, Cl, CF3, or Ci-C3 alkyl, Z is H or F, and R is halogen, C1-C6 alkyl, monohalo C1-C6 alkyl, C3-C6 cycloalkyl, C2-C6 alkenyl, C2-C6 alkynyl, phenyl, monosubstituted phenyl, OR3, 0-C(--.0)R4, or C(=0)0R6.
In additional subgeneric embodiments, this invention provides or contemplates compounds of formulas IA-2, IB-2, IC-2, ID-2, II-B, and III-B, where X is F, Cl, or CH3: Y is I, Br, Cl, CF3, or C1-C3 alkyl, Z is H or F, and R is furyl, thienyl, thiazolyl, isothiazolyl, oxazolyl, isoxazolyl, pyrrolyl, or pyrazolyl.
In additional subgeneric embodiments, this invention provides compounds of formulas IA-2, IB-2, IC-2, ID-2, II-B, and III-B, where X is F, Cl, or CH3; Y
is I, Br, Cl, CF3, or C1-C3 alkyl, Z is H or F, and R is F, Cl, CI-CI alkyl, CI-C3 alkoxy, trifluoromethoxy, or 2-methoxy-ethoxy.
In a more specific subgeneric embodiment, this invention provides a compound of formula IA-1, where Ria is methyl, monohalomethyl, C1-C3 alkoxymethyl, or cyclopropoxymethyl.
In another more specific subgeneric embodiment, this invention provides a compound of formula IA-2, where Rla is methyl, monohalomethyl, C1-C3 alkoxymethyl, or cyclopropoxy methyl and where R ' is F, Cl, C1-C3 alkyl, monochloro C1-C3 alkyl, C1-C3 alkoxy, trifluoro methoxy, or 2-methoxy-ethoxy.
In a more specific subgeneric embodiment of formula IB-1, this invention provides a compound of formula IB-1, where Rib is isopropyl, 2-butyl, 2-pentyl, cyclopropyl, cyclobutyl, cyclopentyl, or cyclohexyl, all optionally substituted with 1 or 2 substituents selected independently from F, Cl, OH, and OCI-13; Y is Br, I, methyl, or trifluoromethyl.
In a more specific subgeneric embodiment of formula IB-2, this invention provides a compound of formula IB-2, where Rib is isopropyl, 2-butyl, 2-pentyl, cyclopropyl, cyclobutyl, cyclopentyl, or cyclohexyl, optionally substituted with 1 or 2 substituents selected independently from F, Cl, OH, and OCH3; Y is Br, I, methyl, or trifluoromethyl; and R ' is F, Cl, Ci-C3 alkyl, monochloro C1-C3 alkyl, Ci-C3 alkoxy, trifluoromethoxy, or 2-methoxy-ethoxy.
In a still more specific subgeneric embodiment of formula IB-1, this invention provides a compound of formula IB-1, where Rib is isopropyl, 2-butyl, 2-pentyl, cyclopropyl, cyclobutyl, cyclopentyl, or cyclohexyl, all optionally substituted with one Cl, with one or with 1 or 2 OH groups; and Y is Br, I, methyl, or trifluoromethyl.
In a more specific subgeneric embodiment of formula IB-2, this invention provides a compound of formula IB-2, where Rib is isopropyl, 2-butyl, 2-pentyl, cyclopropyl, cyclobutyl, cyclopentyl, or cyclohexyl, all optionally substituted with one Cl or with 1 or 2 OH groups; Y is Br, I, methyl, or trifluoromethyl; and R ' is F, Cl, C1-C3 alkyl, monochloro Ci-C3 alkyl, C1-C3 alkoxy, trifluoromethoxy, or 2-methoxy-ethoxy.
In another more specific subgeneric embodiment, this invention provides a compound of formula IC-1 or IC-2, where m is zero, n is 1 or 2, and R' is CI-C.4 alkyl, optionally substituted as described above.
In another more specific subgeneric embodiment, this invention provides a compound of formula IC-1 or IC-2, where m is 1, n is 2 or 3, and R' is Ci-C4 alkyl, optionally substituted as described above.
In a still more specific subgeneric embodiment, this invention provides a compound of formula IC-1 or IC-2, where m is zero, n is 1 or 2, and R' is C1-C4 alkyl, optionally substituted with 1 -3 groups selected from OH, OCH3, Cl, and cyclopropyl.
In another more specific subgeneric embodiment, this invention provides a compound of formula ID-I, where Rid is cycloalkyl or 1-alkyl-cycloalkyl, in which the 1-alkyl group is optionally substituted with one or two OH groups or with one or two halogen atoms.
In another more specific subgeneric embodiment, this invention provides a compound of formula ID-2, where R ' is halogen, C1-C6 alkyl, monohalo C1-C6 alkyl, C3-C6 cycloalkyl, C2-C6 alkenyl, C2-C6 alkynyl, phenyl, monosubstituted phenyl, OR3, 0-C(=0)R4, or C(=0)0R5; and Rid is cycloalkyl or 1-alkyl-cycloalkyl, in which the 1-alkyl group is optionally substituted with one or two OH groups or with one or two halogen atoms.
In another more specific subgeneric embodiment, this invention provides a compound of formula ID-2, where R ' is furyl, thienyl, thiazolyl, isothiazolyl, oxazolyl, isoxazolyl, PYrrolyl, or pyrazolY1; and Rid is cycloalkyl or 1-alkyl-cycloalkyl, in which the 1-alkyl group is optionally substituted with one or two OH groups or one or two halogen atoms.
In another more specific subgeneric embodiment, this invention provides a compound of formula ID-1, where Rid is cycloalkyl or 1-alkyl-cycloalkyl, in which the 1-alkyl group is optionally substituted with one or two OH groups, and where Y is Br, I, methyl, or trifluoromethyl.
In another more specific subgeneric embodiment, this invention provides a compound of formula ID-1, where Rid is cycloalkyl or 1-alkyl-cycloalkyl, in which the 1-alkyl group is optionally substituted with one or two fluorine or chlorine atoms, and where Y
is Br, I, methyl, or trifluoromethyl.
In another more specific subgeneric embodiment, this invention provides a compound of formula ID-2, where Rid is cycloalkyl or (1-alkyl)-cycloalkyl, in which the 1-alkyl group is optionally substituted with one or two OH groups, and where R ' is F, Cl, C1-C3 alkyl, monochloro C1-C3 alkyl, C1-C3 alkoxy, trifluoromethoxy, or 2-methoxy-ethoxy.
. In another more specific subgeneric embodiment, this invention provides a compound of formula ID-1, where Rid is tetrahydrofuryl, tetrahydrothienyl, pyrrolidyl, piperidyl, piperazinyl, or morpholyl, each optionally substituted as described above, and where Y is Br, I, methyl, or trifluoromethyl.
In another more specific subgeneric embodiment, this invention provides a compound of formula ID-1, where Rid is oxazolidinyl, thiazolidinyl, isoxazolidinyl, isothiazolidinyl, tetrahydrofuryl, tetrahydrothienyl, pyrrolidyl, piperidyl, piperazinyl, or morpholyl, each optionally substituted as described above, and where Y is Br, I, methyl, or trifluoromethyl.
In another more specific subgeneric embodiment, this invention provides a compound of formula ID-2, where Rid is cyclopropyl or 1-alkyl-cyclopropyl, in which the 1-alkyl group is optionally substituted with one or two OH groups, and where R ' is F, Cl, methyl, ethyl, chloromethyl, C1-C2 alkoxy, trifluoromethoxy, or 2-methoxy-ethoxy.
In an even more specific embodiment, the invention provides a compound of formula ID-1 in which Rid is 1-(monohydroxyalkyl) cycloalkyl.
In another more specific embodiment, the invention provides a compound of formula ID-2 in which Rid is 1-(monohydroxyalkyl) cycloalkyl, where R is F, Cl, methyl, ethyl, chloromethyl, C1-C2 alkoxy, trifluoromethoxy, or 2-methoxy-ethoxy.
In an even more specific embodiment, the invention provides a compound of formula ID-1 in which Rid is 1-(dihydroxyalkyl) cycloalkyl.
In another more specific embodiment, the invention provides a compound of formula ID-2 in which Rid is 1-(dihydroxyalkyl) cycloalkyl, where R ' is F, Cl, methyl, ethyl, chloromethyl, CI-C2 alkoxy, trifluoromethoxy, or 2-methoxy-ethoxy.
In a more specific subgeneric embodiment of formula IIA, this invention provides a compound of formula II-Al, which is a compound of formula II-A, in which U is CR2 and V
is N.
0" NH X
In another more specific, subgeneric embodiment, this invention provides a compound of formula JIB-1, which is a compound of formula II-B, in which U in which U
and V are both N.
R
,N
%
0" NH X
In a more specific, subgeneric embodiment, this invention provides a compound of formula IIA-3, which is a compound of formula IIA in which U is CR2 and V is CR3.
IR, \ 0 OS
''. NH X
H
F Y
F
In a still more specific subgeneric embodiment, this invention provides a compound of formula I, where G is Ari and Ari is phenyl or monosubstituted phenyl, R
is F, methyl, ethyl, C1-C3 alkoxy, trifluoromethoxy, or 2-methoxy-ethoxy; X is F, Cl, or CH3; Y is I; and Z
is F.
In another subgeneric embodiment, this invention provides a compound of formula I, where G is Ari, where Ari is phenyl or monosubstituted phenyl, R is halogen, C1-C6 alkyl, C3-C6 cycloalkyl, C2-C6 alkenyl, C2-C6 alkynyl, all such alkyl, cycloalkyl, alkenyl, and alkynyl groups optionally substituted with 1-3 substituents selected independently from halogen, OH, CN, cyanomethyl, nitro, phenyl, and trifluoromethyl; or R is phenyl, OR3, furyl, thienyl, thiazolyl, isothiazolyl, oxazolyl, isoxazolyl, pyrrolyl, or pyrazolyl.
In a more specific subgeneric embodiment, this invention provides a compound of formula I, where A is Ari, where Ari is phenyl or monosubstituted phenyl, R
is F, Cl, Ci-C3 alkyl, C1-C3 alkoxy, 2-methoxyethoxy, C2-C3 alkenyl, C2-C3 alkynyl, trifluoromethyl, phenyl, furyl, or thienyl. thiazolyl, isothiazolyl, oxazolyl, isoxazolyl, pyrrolyl, or pyrazolyl; X is F, Cl, or methyl; Y is I, Br, Cl, CF3, or C1-C3 alkyl; and Z is F.
In another still more specific subgeneric embodiment, this invention provides G
compound of formula I, where G is Ari, where An is phenyl or monosubstituted phenyl, R is H; X is F, Cl, or CH3; Y is Br or I; and Z is F.
In another subgeneric embodiment his invention provides G compound of formula I, where G is Ar2, where Ar2 is 2-thienyl, 2-furyl, 3-thienyl, 3-furyl, 2-pyrrolyl, or 3-pyrrolyl, =
all optionally substituted with methoxycarbonyl, methylcarbamoyl, acetamido, acetyl, methyl, ethyl, trifluoromethyl, or halogen.
In a more specific subgeneric embodiment his invention provides 0 compound of formula I, where 0 is Ar2, where Ar2 is 2-thienyl, 2-furyl, 3-thienyl, 3-furyl, 2-pyrrolyl, or 3-pyrrolyl, all optionally substituted with methoxycarbonyl, methylcarbamoyl, acetamido, acetyl, methyl, ethyl, trifluoromethyl, or halogen; R is other than H; X is F, Cl, or CH3: Y is I, Br, Cl, CF3, or C1-C3 alkyl, and Z is H or F.
In another subgeneric embodiment his invention provides G compound of formula I, where 0 is Ar2, where Ar2 is 2-thienyl, 2-fury!, 3-thienyl, 3-fury!, 2-pyrrolyl, or 3-pyrrolyl, all optionally substituted with methoxycarbonyl, methylcarbamoyl, acetamido, acetyl, methyl, ethyl, trifluoromethyl, or halogen; R is F, Cl, Ci-C3 alkyl, monochloro Ci-C3 alkyl, C1-C3 alkoxy, trifluoromethoxy, methyloxy-methoxy, or 2-methoxy-ethoxy; X is F, Cl, or CH3: Y is I, Br, Cl, CF3, or CI-C3 alkyl, and Z is H or F.
In another subgeneric embodiment his invention provides G compound of formula I, where G is Ar2, where Ar2 is 2-thienyl, 2-furyl, 3-thienyl, 3-fury!, 2-pyrrolyl, or 3-pyrrolyl, all optionally substituted with methoxycarbonyl, methylcarbamoyl, acetamido, acetyl, methyl, ethyl, trifluoromethyl, or halogen; R is H; Xis F, CI, or CH3: Y is I, Br, CI, CF3, or C1-C3 alkyl, and Z is H or F.
In another subgeneric embodiment his invention provides G compound of formula I, where G is Ar2, where Ar2 is thiazolyl, isothiazolyl, oxazolyl, isoxazolyl, pyrrolyl, or pyrazolyl, all optionally substituted with methoxycarbonyl, methylcarbamoyl, acetamido, acetyl, methyl, ethyl, trifluoromethyl, or halogen; R is H or methoxy; X is F, Cl, or CH3: Y
is I, Br, Cl, CF3, or C1-C3 alkyl, and Z is H or F.
According to specific embodiments, the present invention relates to a compound which is selected from the compounds below _________________ /
NH
N
NH
OH
Otyl NH
> o N' I
OH
s,0 0', NH
18a OH
0'=7 'NH
"NH
F .1cc OH
OH OH
OH
\
NH
0" "'NH
and iLsOH õ70 \ NH
ON
According to a more specific embodiment, the present invention relates to the compound OH
HO
//
N
o NH
--O NH
18b where the 2-0H carbon is in the R or S configuration.
In a further and more specific embodiment, the invention relates to (S)-N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)-6-methoxypheny1)-1-(2,3-dihydroxypropyl)cyclopropane-l-sulfonamide.
18c Detailed description of the invention As used herein a "pharmaceutically acceptable salt" includes salts that retain the biological effectiveness of the free acids and bases of the specified compound and that are not biologically or otherwise undesirable. A compound of this invention may possess acidic or basic groups and therefore may react with any of a number of inorganic or organic bases, and inorganic and organic acids, to form a pharmaceutically acceptable salt.
Examples of pharmaceutically acceptable salts include those salts prepared by reaction of the compounds of this invention with a mineral or organic acid or an inorganic base, such salts including sulfates, pyrosulfates, bisulfates, sulfites, bisulfites, phosphates, monohydrogenphosphates, dihydrogenphosphates, metaphosphates, pyrophosphates, chlorides, bromides, iodides, acetates, propionates, decanoates, caprylates, acrylates, formates, isobutyrates, caproates, heptanoates, propiolates, oxalates, malonates, succinates, suberates, sebacates, fumarates, maleates, butyn-1,4-dioates, hexyne-1,6-dioates, benzoates, chlorobenzoates, methylbenzoates, dinitrobenzoates, hydroxybenzoates, methoxybenzoates, phthalates, sulfonates, xylenesulfonates, phenylacetates, phenylpropionates, phenylbutyrates, citrates, lactates, .y-hydroxybutyrates, glycollates, tartrates, methanesulfonates, propanesulfonates, naphthalene-l-sulfonates, naphthalene-2-sulfonates, and mandelates.
As used herein, a "prodrug" is a compound that may be converted under physiological conditions or by solvolysis to the specified compound or to a pharmaceutically acceptable salt of such compound. Prodrugs include compounds wherein an amino acid residue, or a polypeptide chain of two or more amino acid residues, is covalently joined through an amide or ester bond to a free amino, hydroxy, or carboxylic acid group of compounds of Formulas I.
The amino acid residues contemplated include but are not limited to the 20 naturally-occurring amino acids. Other suitable amino acids include 4-hydroxyproline, hydroxylysine, demosine, isodemosine, 3-methyl histidine, norvaline, 13-alanine, 7-aminobutyric acid, cirtulline, homocysteine, homoserine, omithine and methionine sulfone.
Additional types of prodrugs are well known in the art.
The tables below show the individual compounds provided or contemplated by this invention.
Table I shows embodiments of this invention which are compounds of formula IA-1.
Table 1: Embodiments According to Formula IA-1 Ria X Y Z
CH3 F Br F
CH3 Cl Br F
CH3 Cl CF3 F
CH3 F CE--=-CH F
CH3 CI C:=-CH F
CH3 Cl SCH3 F
CH3 F (CH2)2CH3 F
CH3 Cl (CH2)2CH3 F
CH3 Cl CH2CH3 F
CH3 Cl CH2OH F
> F
CH3 Cl I> F
CH3 CH3 CH:=CH2 F
CH2F Cl I F
CH2F F Br F
CH2F CI Br F
CH2F Cl CH3 F
CH2F Cl CF3 F
CF3 Cl I F
CF3 F Br F
CF3 Cl Br F
CF3 Cl CH3 F
CF3 Cl CF3 F
Ria X Y Z
CH2CI F _ I F
CH2CI Cl _ 1 F
CH2C1 F Br F
CH2CI Cl Br F
CH2C1 Cl CH3 F
CH2C1 Cl CF3 F
CHCl2 F I F
CHC12 Cl I F
CHC12 F Br F
CHC12 Cl Br F
CHCl2 F CH3 F
CHC12 Cl CH3 F
CHC12 Cl CF3 F
CC13 Cl I F
CC13 F Br F
CC13 Cl Br F
CC13 Cl CH3 F
CC13 H Cl CF3 F
CH2OH Cl I F
CH2OH _ F Br F
CH2OH Cl Br F
CH2OH Cl CH3 F
CH2OH Cl CF3 F
CH20Me F I F
CH20Me Cl I F
CH20Me F Br F
CH20Me - Cl Br F
CH20Me F CH3 F
CH20Me Cl CH3 F
CH20Me F CF3 F
CH20Me Cl CF3 F .
CH20Me F CE-CH F
CH20Me Cl SCH3 F
Ria X V Z
CH20Me CH3 CF3 F
CH20Me CH3 C--CH F
CH20Et F I F
CH20Et Cl I F
CH20Et F Br F
CH20Et CI Br F
CH20Et F cH3 F
CH20Et Cl CH3 F
CH20Et F CF3 F
CH20Et Cl CF3 F
CH20-4 Cl I F
CH20-4 F Br F
CH204 Cl Br F
CH204 Cl CF3 F
Cl I F
CH20 ¨
F
CH20 ¨ Br F
Cl Br F
CH20 ¨
CH20 ¨
Cl CH3 F
¨
CH20 ¨
¨
F
CH2O()H Cl I F
CH20 F Br F
Cl Br F
CH20 oH
C
CH 2 0.-OH CI CH3 F
C
CH2 0OH Cl CF3 F
Ria X Y Z
CH20.0Me F I F
CH20'OMe Ci I F
CH20''.(:)Me F Br F
CH20.0Me Cl Br F
CH200Me F CH3 F
CH20''''OMe CI CH F
CH20OMe F CF3 F
CH20OMe Cl CF3 F
_ (-OH F I F
CH2u \---OH
_ r OH Cl I F
CH2o \¨OH
COH F Br F
CH2 ____________________ OH
0 r OH Cl Br F
CH2 ____________________ \--OH
.... (-OH F CH3 F
CH2u \--OH
.... r OH Cl CH3 F
\--OH
_ r OH F CF3 F
CH2u \---OH
_ _ (-OH Cl CF3 F
CH2o \---OH
Table 2: Embodiments According to Formula IB
Rib X Y Z
I> F I F
I> Cl I F
I> F Br F
I> Cl Br F
I> F CH3 F
Rib X Y Z
> CI CH3 F
> F CF3 F
> Cl CF3 F
> F CF--CH F
> Cl CmCH F
> F SCH3 F
> Cl SCH3 F
> F CH2OH F
> CI CH2OH F
> F (CH2)3014 F
> Cl (CH2)30H F
> F (CH2)2CH3 F
> Cl (CH2)2CH3 F
> F CH2CH3 F
> Cl CH2CH3 F
> F (CH2)2CH3 F
> Cl (CH2)2CH3 F
> CH3 I F
> CH3 Br F
> CH3 CH3 F
> CH3 CF3 F
> CH3 CH2CH3 F
> CH3 (CH2)2CH3 F
> CH3 C.-CH F
> CH3 SCH3 F
CI Cl (CH2)2CH3 F
.."1 > F CH=CH2 F
> Cl CH=CH2 F
, Rib X Y Z
O CH3 CH=CH2 F
I> F I> F
I> F OCH3 F
I> Cl (C112)2CH2OH F
O F I F
O Cl I F
O F Br F
O Cl Br F
O Cl CH F
O Cl CF3 F
O Cl I F
0 F Br F
0 Cl Br F
0 Cl CH3 F
C> F CF3 F
C) Cl CF3 F
O Cl I> F
:3 F (CH2)2CH3 F
OH Cl Ca=CH F
CI' Rlb X Y Z
,,t0CF13 Cl CF3 F
CI' r__OH Cl (CH2)30H F
1----<
F OCH2CH3 ' F
\SD?
CI' 0 Cl I F
0 F Br F
0 Cl Br F
0 Cl CH3 F
0 Cl CF3 F
Table 3 shows embodiments according to formula IC
Table 3 Embodiments According to Formula IC
R1c X Y Z
CH2CH3 Cl I F _ CH2CH3 F Br F
CH2CH3 Cl Br F _ CH2CH3 Cl CH3 F
R1c X Y Z
CH2CH3 Cl CF3 F
CH2CH3 CH3 C:-=-CH F
CH2CH3 F C-:aCH F
CH2CH3 Cl SCH3 F
> F
CH2CH3 Cl > F
> F
CH(CH3)2 F OCH3 F
CH(CH3)2 Cl OCH3 F
CH(CH3)2 F I F
CH(CH3)2 Cl I F
CH(CH3)2 F Br F
CH(CH3)2 Cl Br F
CH(CH3)2 F CH3 F
CH(CH3)2 Cl CH3 F
CH(CH3)2 F CH2CH3 F
CH(CH3)2 Cl CH2CH3 F
CH(CH3)2 CH3 CH2CH3 F
CH(CH3)2 Cl CH2CH3 F
CH(CH3)2 Fl CH(CH3)2 F
CH(CH3)2 Cl CH(CH3)2 F
CH(CH3)2 F CF3 F
CH(CH3)2 Cl CF3 F
CH(CH3)2 CH3 Br F
CH(CH3)2 CH3 C-=CH F
CH(CH3)2 CH3 SCH3 F
CH(CH3)2 CH3 > F
CH(CH3)2 F CH2OH F
CH(CH3)2 Cl OH
_ F
->.
n-butyl F I F
n-butyl Cl I F
n-butyl F Br F
n-butyl Cl Br F
n-butyl F CH3 F
n-butyl Cl CH3 F
=
R1c X Y Z
n-butyl F OCH3 F
n-butyl Cl OCH3 F
n-butyl CH3 OCH3 F
n-butyl Cl OCH2CH3 F
n-butyl F OCH2CH3 F
n-butyl CH3 OCH2CH3 F
n-butyl F OCH2CH2OH F
n-butyl F CF3 F
n-butyl Cl CF3 F
sec-butyl F I F
sec-butyl Cl I F
sec-butyl F Br F
sec-butyl Cl Br F
sec-butyl F CH3 F
sec-butyl Cl CH3 F
sec-butyl F CF3 F
sec-butyl Cl CF3 F
CH2CF3 Cl I F
CH2CF3 F Br F
CH2CF3 Cl Br F
CH2CF3 Cl CH3 F
CH2CF3 Cl CF3 F
CH2CC13 Cl I F
CH2CC13 F Br F
CH2CC13 Cl Br F
CH2CC13 Cl CH3 F
CH2CC13 Cl CF3 F
CH2-4 Cl I F
CH2-4 F Br F
CH2-4 Cl Br F
CH2-4 Cl CH3 F
CH2-4 Cl CF3 F
R1c X Y Z
CH2CH2F F Br F
CH2CH2F Cl Br F
CH2CH2F Cl CH3 F
CH2CH2F Cl CF3 F
CH2CH2C1 Cl I F
CH2CH2C1 F Br F
CH2CH2C1 Cl Br F
CH2CH2C1 Cl CH3 F
CH2CH2C1 Cl CF3 F
CH2CH2CH2CI Cl I F
CH2CH2CH2C1 F Br F
CH2CH2CH2C1 Cl Br F
CH2CH2CH2C1 Cl CF3 F
CH2CH2OH Cl I F
CH2CH2OH F Br F
_ CH2CH2OH Cl Br F
CH2CH2OH Cl CH3 F
CH2CH2CH2OH Cl I F
CH2CH2CH2OH F Br F
CH2CH2CH2OH Cl Br F
CH2CH2CH2OH Cl CH3 F
CH2CH2CH2OH Cl CF3 F
Ri c X Y Z
(CH2)40H F I F
(CH2)40H CI I F
(CH2)40H F Br F
(CH2)40H Cl Br F
(CH2)40H F CH3 F
(CH2)40H Cl CH F
(CH2)40H F CF3 F
(CH2)40H Cl CF3 F
CH2CH2OCH3 Cl I F
CH2CH2OCH3 F Br F
CH2CH2OCH3 Cl Br F
CH2CH2OCH3 Cl CH3 F
CH2CH2OCH3 Cl CF3 F
(CH2)30CH3 F I F
(CH2)30CH3 Cl I F
(CH2)30CH3 F Br F
(CH2)30CH3 Cl Br F
(CH2)30CH3 F CH3 F
(CH2)30CH3 Cl CH3 F
(CH2)30CH3 F CF3 F
(CH2)30CH3 Cl CF3 F
CH2CH20Et F I F
CH2CH20Et Cl I F
CH2CH20Et F Br F
CH2CH20Et Cl Br F
CH2CH20Et F CH3 F
CH2CH20Et Cl CH3 F
CH2CH20Et F CF3 F
CH2CH20Et Cl CF3 F
CH2CH20¨ F I F
CH2CH20¨< Cl I F
CH2CH20¨ F Br F
CH2CH20¨< Cl Br F
CH2CH20¨ F CH3 F
CH2CH20¨ Cl CH3 F
R1c X Y Z
CH2CH20- Cl CF3 F
CH2CH20 < F I F
Cl I F
<
F Br F
<
CH2CH20 < Cl Br F
<
Cl CH3 F
CH2CH20 <
CH2CH20 < F CF3 F
Cl CF3 F
CH2CH20 <
CH2CH2CH20Et F I F
CH2CH2CH20Et Cl I F
CH2CH2CH20Et F Br F
CH2CH2CH20Et Cl Br F
CH2CH2CH20Et F CH3 F
CH2CH2CH20Et Cl CH3 F
CH2CH2CH20Et F CF3 F
CH2CH2CH20Et Cl CF3 F
_ _< F I F
Cl I F
CH2CH2CHF-0-( Br F
CH2CH2CH2-0--( F
Cl Br F
CH2CH2CHi---0-_ < F CH3 F
Cl CH3 F
CH2CH2CHF-0-( CH2CH2CH2 O_\
_ F CF3 F
CH2CH2CHT-0--K Ci R1c X Y Z
Cl CI I F
CH2CH2CHF-(1-4 F Br F
CH2CH2CHn_< Cl Br F
CH2CH2CHT" -4 F CH3 F
Cl CH2CH2CH CH3 F2 -___<CH2CH2CH-2-0 Cl CF3 F
CH2CH2-0,0H F I F
OH
CH2CH2-00H Cl I F
OH
0,...T,OH F Br F
OH
(y.,..c..OH Cl Br F
OH
(:),(.0H F CH3 F
OH
oc..OH Cl CH3 F
OH
(y-,c,.OH F CF3 F
OH
CH2CH2-0H Cl CF3 F
OH
OH F I F
CH/OH
OH Cl I F
OH F Br F
CH/-OH
OH Cl Br F
Ric X
OH Cl CH3 F -OH Cl CF3 OH
CHc'Y'OH
OH
OH Cl CHIY.-OH
OH
CH1-Y'OH
OH
OH F Br OH
OH Cl Br CH2-'0H
OH
OH CH3 Br OH
OH
OH Cl CH3 CH?'`r'OH
OH
OH
OH F C-aCH
CH2-'(OH
OH
CH/OH
OH
CHI'Y'OH
OH
OH Cl CH2CH(OH)CH3 F
OH
OH F CH(CH3)2 CH2r-OH
OH
R1c X Y Z
OH Cl CF3 F
CH2'"Cr*OH
OH
Tables 4a and 4b present species according to formula I, where A = Rid, except where Rid is heterocyclic; compounds of that type are presented in Table 5. Each line in the table corresponds to five species which differ only at position Y.
TABLE 4a SPECIES CORRESPONDING TO A = Rid A' B
A/\10 =S( H
F Ya,b, c, or d F
Ya = CI-13; Yb'="- Br; Y0 = I; Yd = Cl;
CMPD # A, A' B R
1 (a-d) H, H H OCH3 2 (a-d) H, H H NHCH3 3 (a-d) H, H H CH2CH3 4 (a-d) H, H H
CH2CH=CH2 5 (a-d) H, H H CN
6 (a-d) H, H H CF3 7(a-d) H, H H F
8(a-d) H, H H C6H6 9(a-d) H, H -CH2CH(OH)CH2OH
NH
where Rid is C(A)(A')(B)- where B, A, and A' are, independently, H or C1-4 alkyl, optionally substituted with one or two OH groups or halogen atoms, or A and A', together with the carbon atom to which they are attached, form a 3- to 6- member saturated ring, said ring optionally containing one or two heteroatoms selected, independently, from 0, N, and S and optionally substituted with one or two groups selected independently from methyl, ethyl, and halo In another embodiment, the invention provides a compound of formula ID-2, Rlet //0 // N X
Ro' NH
where Rid is defined as above and where R ' is R , defined above, other than H.
In another embodiment, this invention provides a compound of formula IE-1.
,0 // N X
where Rie is defined as above.
In another embodiment, this invention provides a compound of formula 1E-2, R1 e Ro' 00 NH
where R ' is R , defined above, other than H.
In another embodiment, this invention provides a compound of formula II-A, where G.
is An, NH
II-A
where R2-6, U, and V are defined as above.
In another embodiment, this invention provides a compound of formula II-B, SN
II-B
where R ' is R , defined above, other than H.
In another embodiment, this invention provides a compound of formula III-A
..V/R7-8 li---Z-st."¨S/
//N
Z Y
F
III-A
In another embodiment, this invention provides a compound of formula 111-13 R7_8 erV/S/ 0 - / h Ul--....177-----gf //N
Z Y
F
III-B
where R ' is R , defined above, other than H.
In additional subgeneric embodiments, this invention provides compounds of formulas IA-1, IA-2, 1B-1, I13-2, IC-1, IC-2, ID-1, ID2, II-A, II-B, III-A, and III-B, where X
is F, Cl, or CH3: Y is I, Br, Cl, CF3, or C1-C3 alkyl, and Z is H or F.
In additional subgeneric embodiments, this invention provides compounds of formulas IA-2, IB-2, IC-2, ID-2, II-B, and III-B, where X is F, Cl, or CH3: Y
is I, Br, Cl, CF3, or Ci-C3 alkyl, Z is H or F, and R is halogen, C1-C6 alkyl, monohalo C1-C6 alkyl, C3-C6 cycloalkyl, C2-C6 alkenyl, C2-C6 alkynyl, phenyl, monosubstituted phenyl, OR3, 0-C(--.0)R4, or C(=0)0R6.
In additional subgeneric embodiments, this invention provides or contemplates compounds of formulas IA-2, IB-2, IC-2, ID-2, II-B, and III-B, where X is F, Cl, or CH3: Y is I, Br, Cl, CF3, or C1-C3 alkyl, Z is H or F, and R is furyl, thienyl, thiazolyl, isothiazolyl, oxazolyl, isoxazolyl, pyrrolyl, or pyrazolyl.
In additional subgeneric embodiments, this invention provides compounds of formulas IA-2, IB-2, IC-2, ID-2, II-B, and III-B, where X is F, Cl, or CH3; Y
is I, Br, Cl, CF3, or C1-C3 alkyl, Z is H or F, and R is F, Cl, CI-CI alkyl, CI-C3 alkoxy, trifluoromethoxy, or 2-methoxy-ethoxy.
In a more specific subgeneric embodiment, this invention provides a compound of formula IA-1, where Ria is methyl, monohalomethyl, C1-C3 alkoxymethyl, or cyclopropoxymethyl.
In another more specific subgeneric embodiment, this invention provides a compound of formula IA-2, where Rla is methyl, monohalomethyl, C1-C3 alkoxymethyl, or cyclopropoxy methyl and where R ' is F, Cl, C1-C3 alkyl, monochloro C1-C3 alkyl, C1-C3 alkoxy, trifluoro methoxy, or 2-methoxy-ethoxy.
In a more specific subgeneric embodiment of formula IB-1, this invention provides a compound of formula IB-1, where Rib is isopropyl, 2-butyl, 2-pentyl, cyclopropyl, cyclobutyl, cyclopentyl, or cyclohexyl, all optionally substituted with 1 or 2 substituents selected independently from F, Cl, OH, and OCI-13; Y is Br, I, methyl, or trifluoromethyl.
In a more specific subgeneric embodiment of formula IB-2, this invention provides a compound of formula IB-2, where Rib is isopropyl, 2-butyl, 2-pentyl, cyclopropyl, cyclobutyl, cyclopentyl, or cyclohexyl, optionally substituted with 1 or 2 substituents selected independently from F, Cl, OH, and OCH3; Y is Br, I, methyl, or trifluoromethyl; and R ' is F, Cl, Ci-C3 alkyl, monochloro C1-C3 alkyl, Ci-C3 alkoxy, trifluoromethoxy, or 2-methoxy-ethoxy.
In a still more specific subgeneric embodiment of formula IB-1, this invention provides a compound of formula IB-1, where Rib is isopropyl, 2-butyl, 2-pentyl, cyclopropyl, cyclobutyl, cyclopentyl, or cyclohexyl, all optionally substituted with one Cl, with one or with 1 or 2 OH groups; and Y is Br, I, methyl, or trifluoromethyl.
In a more specific subgeneric embodiment of formula IB-2, this invention provides a compound of formula IB-2, where Rib is isopropyl, 2-butyl, 2-pentyl, cyclopropyl, cyclobutyl, cyclopentyl, or cyclohexyl, all optionally substituted with one Cl or with 1 or 2 OH groups; Y is Br, I, methyl, or trifluoromethyl; and R ' is F, Cl, C1-C3 alkyl, monochloro Ci-C3 alkyl, C1-C3 alkoxy, trifluoromethoxy, or 2-methoxy-ethoxy.
In another more specific subgeneric embodiment, this invention provides a compound of formula IC-1 or IC-2, where m is zero, n is 1 or 2, and R' is CI-C.4 alkyl, optionally substituted as described above.
In another more specific subgeneric embodiment, this invention provides a compound of formula IC-1 or IC-2, where m is 1, n is 2 or 3, and R' is Ci-C4 alkyl, optionally substituted as described above.
In a still more specific subgeneric embodiment, this invention provides a compound of formula IC-1 or IC-2, where m is zero, n is 1 or 2, and R' is C1-C4 alkyl, optionally substituted with 1 -3 groups selected from OH, OCH3, Cl, and cyclopropyl.
In another more specific subgeneric embodiment, this invention provides a compound of formula ID-I, where Rid is cycloalkyl or 1-alkyl-cycloalkyl, in which the 1-alkyl group is optionally substituted with one or two OH groups or with one or two halogen atoms.
In another more specific subgeneric embodiment, this invention provides a compound of formula ID-2, where R ' is halogen, C1-C6 alkyl, monohalo C1-C6 alkyl, C3-C6 cycloalkyl, C2-C6 alkenyl, C2-C6 alkynyl, phenyl, monosubstituted phenyl, OR3, 0-C(=0)R4, or C(=0)0R5; and Rid is cycloalkyl or 1-alkyl-cycloalkyl, in which the 1-alkyl group is optionally substituted with one or two OH groups or with one or two halogen atoms.
In another more specific subgeneric embodiment, this invention provides a compound of formula ID-2, where R ' is furyl, thienyl, thiazolyl, isothiazolyl, oxazolyl, isoxazolyl, PYrrolyl, or pyrazolY1; and Rid is cycloalkyl or 1-alkyl-cycloalkyl, in which the 1-alkyl group is optionally substituted with one or two OH groups or one or two halogen atoms.
In another more specific subgeneric embodiment, this invention provides a compound of formula ID-1, where Rid is cycloalkyl or 1-alkyl-cycloalkyl, in which the 1-alkyl group is optionally substituted with one or two OH groups, and where Y is Br, I, methyl, or trifluoromethyl.
In another more specific subgeneric embodiment, this invention provides a compound of formula ID-1, where Rid is cycloalkyl or 1-alkyl-cycloalkyl, in which the 1-alkyl group is optionally substituted with one or two fluorine or chlorine atoms, and where Y
is Br, I, methyl, or trifluoromethyl.
In another more specific subgeneric embodiment, this invention provides a compound of formula ID-2, where Rid is cycloalkyl or (1-alkyl)-cycloalkyl, in which the 1-alkyl group is optionally substituted with one or two OH groups, and where R ' is F, Cl, C1-C3 alkyl, monochloro C1-C3 alkyl, C1-C3 alkoxy, trifluoromethoxy, or 2-methoxy-ethoxy.
. In another more specific subgeneric embodiment, this invention provides a compound of formula ID-1, where Rid is tetrahydrofuryl, tetrahydrothienyl, pyrrolidyl, piperidyl, piperazinyl, or morpholyl, each optionally substituted as described above, and where Y is Br, I, methyl, or trifluoromethyl.
In another more specific subgeneric embodiment, this invention provides a compound of formula ID-1, where Rid is oxazolidinyl, thiazolidinyl, isoxazolidinyl, isothiazolidinyl, tetrahydrofuryl, tetrahydrothienyl, pyrrolidyl, piperidyl, piperazinyl, or morpholyl, each optionally substituted as described above, and where Y is Br, I, methyl, or trifluoromethyl.
In another more specific subgeneric embodiment, this invention provides a compound of formula ID-2, where Rid is cyclopropyl or 1-alkyl-cyclopropyl, in which the 1-alkyl group is optionally substituted with one or two OH groups, and where R ' is F, Cl, methyl, ethyl, chloromethyl, C1-C2 alkoxy, trifluoromethoxy, or 2-methoxy-ethoxy.
In an even more specific embodiment, the invention provides a compound of formula ID-1 in which Rid is 1-(monohydroxyalkyl) cycloalkyl.
In another more specific embodiment, the invention provides a compound of formula ID-2 in which Rid is 1-(monohydroxyalkyl) cycloalkyl, where R is F, Cl, methyl, ethyl, chloromethyl, C1-C2 alkoxy, trifluoromethoxy, or 2-methoxy-ethoxy.
In an even more specific embodiment, the invention provides a compound of formula ID-1 in which Rid is 1-(dihydroxyalkyl) cycloalkyl.
In another more specific embodiment, the invention provides a compound of formula ID-2 in which Rid is 1-(dihydroxyalkyl) cycloalkyl, where R ' is F, Cl, methyl, ethyl, chloromethyl, CI-C2 alkoxy, trifluoromethoxy, or 2-methoxy-ethoxy.
In a more specific subgeneric embodiment of formula IIA, this invention provides a compound of formula II-Al, which is a compound of formula II-A, in which U is CR2 and V
is N.
0" NH X
In another more specific, subgeneric embodiment, this invention provides a compound of formula JIB-1, which is a compound of formula II-B, in which U in which U
and V are both N.
R
,N
%
0" NH X
In a more specific, subgeneric embodiment, this invention provides a compound of formula IIA-3, which is a compound of formula IIA in which U is CR2 and V is CR3.
IR, \ 0 OS
''. NH X
H
F Y
F
In a still more specific subgeneric embodiment, this invention provides a compound of formula I, where G is Ari and Ari is phenyl or monosubstituted phenyl, R
is F, methyl, ethyl, C1-C3 alkoxy, trifluoromethoxy, or 2-methoxy-ethoxy; X is F, Cl, or CH3; Y is I; and Z
is F.
In another subgeneric embodiment, this invention provides a compound of formula I, where G is Ari, where Ari is phenyl or monosubstituted phenyl, R is halogen, C1-C6 alkyl, C3-C6 cycloalkyl, C2-C6 alkenyl, C2-C6 alkynyl, all such alkyl, cycloalkyl, alkenyl, and alkynyl groups optionally substituted with 1-3 substituents selected independently from halogen, OH, CN, cyanomethyl, nitro, phenyl, and trifluoromethyl; or R is phenyl, OR3, furyl, thienyl, thiazolyl, isothiazolyl, oxazolyl, isoxazolyl, pyrrolyl, or pyrazolyl.
In a more specific subgeneric embodiment, this invention provides a compound of formula I, where A is Ari, where Ari is phenyl or monosubstituted phenyl, R
is F, Cl, Ci-C3 alkyl, C1-C3 alkoxy, 2-methoxyethoxy, C2-C3 alkenyl, C2-C3 alkynyl, trifluoromethyl, phenyl, furyl, or thienyl. thiazolyl, isothiazolyl, oxazolyl, isoxazolyl, pyrrolyl, or pyrazolyl; X is F, Cl, or methyl; Y is I, Br, Cl, CF3, or C1-C3 alkyl; and Z is F.
In another still more specific subgeneric embodiment, this invention provides G
compound of formula I, where G is Ari, where An is phenyl or monosubstituted phenyl, R is H; X is F, Cl, or CH3; Y is Br or I; and Z is F.
In another subgeneric embodiment his invention provides G compound of formula I, where G is Ar2, where Ar2 is 2-thienyl, 2-furyl, 3-thienyl, 3-furyl, 2-pyrrolyl, or 3-pyrrolyl, =
all optionally substituted with methoxycarbonyl, methylcarbamoyl, acetamido, acetyl, methyl, ethyl, trifluoromethyl, or halogen.
In a more specific subgeneric embodiment his invention provides 0 compound of formula I, where 0 is Ar2, where Ar2 is 2-thienyl, 2-furyl, 3-thienyl, 3-furyl, 2-pyrrolyl, or 3-pyrrolyl, all optionally substituted with methoxycarbonyl, methylcarbamoyl, acetamido, acetyl, methyl, ethyl, trifluoromethyl, or halogen; R is other than H; X is F, Cl, or CH3: Y is I, Br, Cl, CF3, or C1-C3 alkyl, and Z is H or F.
In another subgeneric embodiment his invention provides G compound of formula I, where 0 is Ar2, where Ar2 is 2-thienyl, 2-fury!, 3-thienyl, 3-fury!, 2-pyrrolyl, or 3-pyrrolyl, all optionally substituted with methoxycarbonyl, methylcarbamoyl, acetamido, acetyl, methyl, ethyl, trifluoromethyl, or halogen; R is F, Cl, Ci-C3 alkyl, monochloro Ci-C3 alkyl, C1-C3 alkoxy, trifluoromethoxy, methyloxy-methoxy, or 2-methoxy-ethoxy; X is F, Cl, or CH3: Y is I, Br, Cl, CF3, or CI-C3 alkyl, and Z is H or F.
In another subgeneric embodiment his invention provides G compound of formula I, where G is Ar2, where Ar2 is 2-thienyl, 2-furyl, 3-thienyl, 3-fury!, 2-pyrrolyl, or 3-pyrrolyl, all optionally substituted with methoxycarbonyl, methylcarbamoyl, acetamido, acetyl, methyl, ethyl, trifluoromethyl, or halogen; R is H; Xis F, CI, or CH3: Y is I, Br, CI, CF3, or C1-C3 alkyl, and Z is H or F.
In another subgeneric embodiment his invention provides G compound of formula I, where G is Ar2, where Ar2 is thiazolyl, isothiazolyl, oxazolyl, isoxazolyl, pyrrolyl, or pyrazolyl, all optionally substituted with methoxycarbonyl, methylcarbamoyl, acetamido, acetyl, methyl, ethyl, trifluoromethyl, or halogen; R is H or methoxy; X is F, Cl, or CH3: Y
is I, Br, Cl, CF3, or C1-C3 alkyl, and Z is H or F.
According to specific embodiments, the present invention relates to a compound which is selected from the compounds below _________________ /
NH
N
NH
OH
Otyl NH
> o N' I
OH
s,0 0', NH
18a OH
0'=7 'NH
"NH
F .1cc OH
OH OH
OH
\
NH
0" "'NH
and iLsOH õ70 \ NH
ON
According to a more specific embodiment, the present invention relates to the compound OH
HO
//
N
o NH
--O NH
18b where the 2-0H carbon is in the R or S configuration.
In a further and more specific embodiment, the invention relates to (S)-N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)-6-methoxypheny1)-1-(2,3-dihydroxypropyl)cyclopropane-l-sulfonamide.
18c Detailed description of the invention As used herein a "pharmaceutically acceptable salt" includes salts that retain the biological effectiveness of the free acids and bases of the specified compound and that are not biologically or otherwise undesirable. A compound of this invention may possess acidic or basic groups and therefore may react with any of a number of inorganic or organic bases, and inorganic and organic acids, to form a pharmaceutically acceptable salt.
Examples of pharmaceutically acceptable salts include those salts prepared by reaction of the compounds of this invention with a mineral or organic acid or an inorganic base, such salts including sulfates, pyrosulfates, bisulfates, sulfites, bisulfites, phosphates, monohydrogenphosphates, dihydrogenphosphates, metaphosphates, pyrophosphates, chlorides, bromides, iodides, acetates, propionates, decanoates, caprylates, acrylates, formates, isobutyrates, caproates, heptanoates, propiolates, oxalates, malonates, succinates, suberates, sebacates, fumarates, maleates, butyn-1,4-dioates, hexyne-1,6-dioates, benzoates, chlorobenzoates, methylbenzoates, dinitrobenzoates, hydroxybenzoates, methoxybenzoates, phthalates, sulfonates, xylenesulfonates, phenylacetates, phenylpropionates, phenylbutyrates, citrates, lactates, .y-hydroxybutyrates, glycollates, tartrates, methanesulfonates, propanesulfonates, naphthalene-l-sulfonates, naphthalene-2-sulfonates, and mandelates.
As used herein, a "prodrug" is a compound that may be converted under physiological conditions or by solvolysis to the specified compound or to a pharmaceutically acceptable salt of such compound. Prodrugs include compounds wherein an amino acid residue, or a polypeptide chain of two or more amino acid residues, is covalently joined through an amide or ester bond to a free amino, hydroxy, or carboxylic acid group of compounds of Formulas I.
The amino acid residues contemplated include but are not limited to the 20 naturally-occurring amino acids. Other suitable amino acids include 4-hydroxyproline, hydroxylysine, demosine, isodemosine, 3-methyl histidine, norvaline, 13-alanine, 7-aminobutyric acid, cirtulline, homocysteine, homoserine, omithine and methionine sulfone.
Additional types of prodrugs are well known in the art.
The tables below show the individual compounds provided or contemplated by this invention.
Table I shows embodiments of this invention which are compounds of formula IA-1.
Table 1: Embodiments According to Formula IA-1 Ria X Y Z
CH3 F Br F
CH3 Cl Br F
CH3 Cl CF3 F
CH3 F CE--=-CH F
CH3 CI C:=-CH F
CH3 Cl SCH3 F
CH3 F (CH2)2CH3 F
CH3 Cl (CH2)2CH3 F
CH3 Cl CH2CH3 F
CH3 Cl CH2OH F
> F
CH3 Cl I> F
CH3 CH3 CH:=CH2 F
CH2F Cl I F
CH2F F Br F
CH2F CI Br F
CH2F Cl CH3 F
CH2F Cl CF3 F
CF3 Cl I F
CF3 F Br F
CF3 Cl Br F
CF3 Cl CH3 F
CF3 Cl CF3 F
Ria X Y Z
CH2CI F _ I F
CH2CI Cl _ 1 F
CH2C1 F Br F
CH2CI Cl Br F
CH2C1 Cl CH3 F
CH2C1 Cl CF3 F
CHCl2 F I F
CHC12 Cl I F
CHC12 F Br F
CHC12 Cl Br F
CHCl2 F CH3 F
CHC12 Cl CH3 F
CHC12 Cl CF3 F
CC13 Cl I F
CC13 F Br F
CC13 Cl Br F
CC13 Cl CH3 F
CC13 H Cl CF3 F
CH2OH Cl I F
CH2OH _ F Br F
CH2OH Cl Br F
CH2OH Cl CH3 F
CH2OH Cl CF3 F
CH20Me F I F
CH20Me Cl I F
CH20Me F Br F
CH20Me - Cl Br F
CH20Me F CH3 F
CH20Me Cl CH3 F
CH20Me F CF3 F
CH20Me Cl CF3 F .
CH20Me F CE-CH F
CH20Me Cl SCH3 F
Ria X V Z
CH20Me CH3 CF3 F
CH20Me CH3 C--CH F
CH20Et F I F
CH20Et Cl I F
CH20Et F Br F
CH20Et CI Br F
CH20Et F cH3 F
CH20Et Cl CH3 F
CH20Et F CF3 F
CH20Et Cl CF3 F
CH20-4 Cl I F
CH20-4 F Br F
CH204 Cl Br F
CH204 Cl CF3 F
Cl I F
CH20 ¨
F
CH20 ¨ Br F
Cl Br F
CH20 ¨
CH20 ¨
Cl CH3 F
¨
CH20 ¨
¨
F
CH2O()H Cl I F
CH20 F Br F
Cl Br F
CH20 oH
C
CH 2 0.-OH CI CH3 F
C
CH2 0OH Cl CF3 F
Ria X Y Z
CH20.0Me F I F
CH20'OMe Ci I F
CH20''.(:)Me F Br F
CH20.0Me Cl Br F
CH200Me F CH3 F
CH20''''OMe CI CH F
CH20OMe F CF3 F
CH20OMe Cl CF3 F
_ (-OH F I F
CH2u \---OH
_ r OH Cl I F
CH2o \¨OH
COH F Br F
CH2 ____________________ OH
0 r OH Cl Br F
CH2 ____________________ \--OH
.... (-OH F CH3 F
CH2u \--OH
.... r OH Cl CH3 F
\--OH
_ r OH F CF3 F
CH2u \---OH
_ _ (-OH Cl CF3 F
CH2o \---OH
Table 2: Embodiments According to Formula IB
Rib X Y Z
I> F I F
I> Cl I F
I> F Br F
I> Cl Br F
I> F CH3 F
Rib X Y Z
> CI CH3 F
> F CF3 F
> Cl CF3 F
> F CF--CH F
> Cl CmCH F
> F SCH3 F
> Cl SCH3 F
> F CH2OH F
> CI CH2OH F
> F (CH2)3014 F
> Cl (CH2)30H F
> F (CH2)2CH3 F
> Cl (CH2)2CH3 F
> F CH2CH3 F
> Cl CH2CH3 F
> F (CH2)2CH3 F
> Cl (CH2)2CH3 F
> CH3 I F
> CH3 Br F
> CH3 CH3 F
> CH3 CF3 F
> CH3 CH2CH3 F
> CH3 (CH2)2CH3 F
> CH3 C.-CH F
> CH3 SCH3 F
CI Cl (CH2)2CH3 F
.."1 > F CH=CH2 F
> Cl CH=CH2 F
, Rib X Y Z
O CH3 CH=CH2 F
I> F I> F
I> F OCH3 F
I> Cl (C112)2CH2OH F
O F I F
O Cl I F
O F Br F
O Cl Br F
O Cl CH F
O Cl CF3 F
O Cl I F
0 F Br F
0 Cl Br F
0 Cl CH3 F
C> F CF3 F
C) Cl CF3 F
O Cl I> F
:3 F (CH2)2CH3 F
OH Cl Ca=CH F
CI' Rlb X Y Z
,,t0CF13 Cl CF3 F
CI' r__OH Cl (CH2)30H F
1----<
F OCH2CH3 ' F
\SD?
CI' 0 Cl I F
0 F Br F
0 Cl Br F
0 Cl CH3 F
0 Cl CF3 F
Table 3 shows embodiments according to formula IC
Table 3 Embodiments According to Formula IC
R1c X Y Z
CH2CH3 Cl I F _ CH2CH3 F Br F
CH2CH3 Cl Br F _ CH2CH3 Cl CH3 F
R1c X Y Z
CH2CH3 Cl CF3 F
CH2CH3 CH3 C:-=-CH F
CH2CH3 F C-:aCH F
CH2CH3 Cl SCH3 F
> F
CH2CH3 Cl > F
> F
CH(CH3)2 F OCH3 F
CH(CH3)2 Cl OCH3 F
CH(CH3)2 F I F
CH(CH3)2 Cl I F
CH(CH3)2 F Br F
CH(CH3)2 Cl Br F
CH(CH3)2 F CH3 F
CH(CH3)2 Cl CH3 F
CH(CH3)2 F CH2CH3 F
CH(CH3)2 Cl CH2CH3 F
CH(CH3)2 CH3 CH2CH3 F
CH(CH3)2 Cl CH2CH3 F
CH(CH3)2 Fl CH(CH3)2 F
CH(CH3)2 Cl CH(CH3)2 F
CH(CH3)2 F CF3 F
CH(CH3)2 Cl CF3 F
CH(CH3)2 CH3 Br F
CH(CH3)2 CH3 C-=CH F
CH(CH3)2 CH3 SCH3 F
CH(CH3)2 CH3 > F
CH(CH3)2 F CH2OH F
CH(CH3)2 Cl OH
_ F
->.
n-butyl F I F
n-butyl Cl I F
n-butyl F Br F
n-butyl Cl Br F
n-butyl F CH3 F
n-butyl Cl CH3 F
=
R1c X Y Z
n-butyl F OCH3 F
n-butyl Cl OCH3 F
n-butyl CH3 OCH3 F
n-butyl Cl OCH2CH3 F
n-butyl F OCH2CH3 F
n-butyl CH3 OCH2CH3 F
n-butyl F OCH2CH2OH F
n-butyl F CF3 F
n-butyl Cl CF3 F
sec-butyl F I F
sec-butyl Cl I F
sec-butyl F Br F
sec-butyl Cl Br F
sec-butyl F CH3 F
sec-butyl Cl CH3 F
sec-butyl F CF3 F
sec-butyl Cl CF3 F
CH2CF3 Cl I F
CH2CF3 F Br F
CH2CF3 Cl Br F
CH2CF3 Cl CH3 F
CH2CF3 Cl CF3 F
CH2CC13 Cl I F
CH2CC13 F Br F
CH2CC13 Cl Br F
CH2CC13 Cl CH3 F
CH2CC13 Cl CF3 F
CH2-4 Cl I F
CH2-4 F Br F
CH2-4 Cl Br F
CH2-4 Cl CH3 F
CH2-4 Cl CF3 F
R1c X Y Z
CH2CH2F F Br F
CH2CH2F Cl Br F
CH2CH2F Cl CH3 F
CH2CH2F Cl CF3 F
CH2CH2C1 Cl I F
CH2CH2C1 F Br F
CH2CH2C1 Cl Br F
CH2CH2C1 Cl CH3 F
CH2CH2C1 Cl CF3 F
CH2CH2CH2CI Cl I F
CH2CH2CH2C1 F Br F
CH2CH2CH2C1 Cl Br F
CH2CH2CH2C1 Cl CF3 F
CH2CH2OH Cl I F
CH2CH2OH F Br F
_ CH2CH2OH Cl Br F
CH2CH2OH Cl CH3 F
CH2CH2CH2OH Cl I F
CH2CH2CH2OH F Br F
CH2CH2CH2OH Cl Br F
CH2CH2CH2OH Cl CH3 F
CH2CH2CH2OH Cl CF3 F
Ri c X Y Z
(CH2)40H F I F
(CH2)40H CI I F
(CH2)40H F Br F
(CH2)40H Cl Br F
(CH2)40H F CH3 F
(CH2)40H Cl CH F
(CH2)40H F CF3 F
(CH2)40H Cl CF3 F
CH2CH2OCH3 Cl I F
CH2CH2OCH3 F Br F
CH2CH2OCH3 Cl Br F
CH2CH2OCH3 Cl CH3 F
CH2CH2OCH3 Cl CF3 F
(CH2)30CH3 F I F
(CH2)30CH3 Cl I F
(CH2)30CH3 F Br F
(CH2)30CH3 Cl Br F
(CH2)30CH3 F CH3 F
(CH2)30CH3 Cl CH3 F
(CH2)30CH3 F CF3 F
(CH2)30CH3 Cl CF3 F
CH2CH20Et F I F
CH2CH20Et Cl I F
CH2CH20Et F Br F
CH2CH20Et Cl Br F
CH2CH20Et F CH3 F
CH2CH20Et Cl CH3 F
CH2CH20Et F CF3 F
CH2CH20Et Cl CF3 F
CH2CH20¨ F I F
CH2CH20¨< Cl I F
CH2CH20¨ F Br F
CH2CH20¨< Cl Br F
CH2CH20¨ F CH3 F
CH2CH20¨ Cl CH3 F
R1c X Y Z
CH2CH20- Cl CF3 F
CH2CH20 < F I F
Cl I F
<
F Br F
<
CH2CH20 < Cl Br F
<
Cl CH3 F
CH2CH20 <
CH2CH20 < F CF3 F
Cl CF3 F
CH2CH20 <
CH2CH2CH20Et F I F
CH2CH2CH20Et Cl I F
CH2CH2CH20Et F Br F
CH2CH2CH20Et Cl Br F
CH2CH2CH20Et F CH3 F
CH2CH2CH20Et Cl CH3 F
CH2CH2CH20Et F CF3 F
CH2CH2CH20Et Cl CF3 F
_ _< F I F
Cl I F
CH2CH2CHF-0-( Br F
CH2CH2CH2-0--( F
Cl Br F
CH2CH2CHi---0-_ < F CH3 F
Cl CH3 F
CH2CH2CHF-0-( CH2CH2CH2 O_\
_ F CF3 F
CH2CH2CHT-0--K Ci R1c X Y Z
Cl CI I F
CH2CH2CHF-(1-4 F Br F
CH2CH2CHn_< Cl Br F
CH2CH2CHT" -4 F CH3 F
Cl CH2CH2CH CH3 F2 -___<CH2CH2CH-2-0 Cl CF3 F
CH2CH2-0,0H F I F
OH
CH2CH2-00H Cl I F
OH
0,...T,OH F Br F
OH
(y.,..c..OH Cl Br F
OH
(:),(.0H F CH3 F
OH
oc..OH Cl CH3 F
OH
(y-,c,.OH F CF3 F
OH
CH2CH2-0H Cl CF3 F
OH
OH F I F
CH/OH
OH Cl I F
OH F Br F
CH/-OH
OH Cl Br F
Ric X
OH Cl CH3 F -OH Cl CF3 OH
CHc'Y'OH
OH
OH Cl CHIY.-OH
OH
CH1-Y'OH
OH
OH F Br OH
OH Cl Br CH2-'0H
OH
OH CH3 Br OH
OH
OH Cl CH3 CH?'`r'OH
OH
OH
OH F C-aCH
CH2-'(OH
OH
CH/OH
OH
CHI'Y'OH
OH
OH Cl CH2CH(OH)CH3 F
OH
OH F CH(CH3)2 CH2r-OH
OH
R1c X Y Z
OH Cl CF3 F
CH2'"Cr*OH
OH
Tables 4a and 4b present species according to formula I, where A = Rid, except where Rid is heterocyclic; compounds of that type are presented in Table 5. Each line in the table corresponds to five species which differ only at position Y.
TABLE 4a SPECIES CORRESPONDING TO A = Rid A' B
A/\10 =S( H
F Ya,b, c, or d F
Ya = CI-13; Yb'="- Br; Y0 = I; Yd = Cl;
CMPD # A, A' B R
1 (a-d) H, H H OCH3 2 (a-d) H, H H NHCH3 3 (a-d) H, H H CH2CH3 4 (a-d) H, H H
CH2CH=CH2 5 (a-d) H, H H CN
6 (a-d) H, H H CF3 7(a-d) H, H H F
8(a-d) H, H H C6H6 9(a-d) H, H -CH2CH(OH)CH2OH
10(a-d) H, H -CH2CH(OH)CH2OH
11(a-d) H, H -CH2CH(OH)CH2OH
12(a-d) -(CH2)2- -CH2(C3H5) 0CH3
13(a-d) -(CH2)2- -CH2(C3H5) NHCH3
14(a-d) -(CH2)2- -CH2(C3H5) CH2CH3
15(a-d) -(CH2)2- CH3 F
16(a-d) -(CH2)2- -CH2CH2OH F
17(a-d) -(CH2)2- -(CH2)2CH(OH)CH2OH
F
F
18(a-d) CH3, H -(CH2)2CH(OH)CH2OH
F
F
19(a-d) -(CH2)2- CH3 OCH3
20(a-d) -(CH2)2- -CH2CH2OH OCH3
21(a-d) -(CH2)2- -(CH2)2CH(OH)CH2OH
_ CMPD # A, A' B R
_ CMPD # A, A' B R
22(a-d) CH3, H -(CH2)2CH(OH)CH2OH
23(a-d) -(CH2)2- CH3 H
24(a-d) -(CH2)2- -CH2CH2OH H
25(a-d) -(CH2)2- -(CH2)2CH(OH)CH2OH
H
H
26(a-d) CH3, H -(CH2)2CH(OH)CH2OH
H
ClVfPD # A, A' B R
1 (a-d) H, H H 2-furanyl 2(a-d) H, H H 1,2,3 triazoly1-4-y1 3(a-d) H, H H 4-imidazoly1 4(a-d) H, H H 2-furanyl 5(a-d) H, H H 1,2,3 triazoly1-4-y1 6(a-d) H, H H 4-imidazoly1 7(a-d) H, H -CH2CH(OH)CH2OH 2-furanyl 8(a-d) H, H -CH2CH(OH)CH2OH
1,2,3 triazoly1-4-y1 9(a-d) H, H -CH2CH(OH)CH2OH 4-imidazoly1 10(a-d) -(CH2)2- -CH2(C3H5) 2-furanyl 11(a-d) -(CH2)2- -CH2(C3H5) 1,2,3 triazoly1-4-y1 12(a-d) -(CH2)2- -CH2(C31-15) 4-imidazoly1 13(a-d) -(CH2)2- CH3 4-thiazoly1 14(a-d) -(CH2)2- -CH2CH2OH 4-thiazoly1 15(a-d) -(CH2)2- -(CH2)2CH(OH)CH2OH
4-thiazoly1 16(a-d) CH3, H -(CH2)2CH(OH)CH2OH
4-thiazoly1 17(a-d) -(CH2)2- CH3 2-oxazoly1 18(a-d) -(CH2)2- -CH2CH2OH 2-oxazoly1 19(a-d) -(CH2)2- -(CH2)2CH(OH)CH2OH
2-oxazoly1 20(a-d) CH3, H -(CH2)2CH(OH)CH2OH
2-oxazoly1 Table 5 presents species of formulas II-A, and III-A, and also species of generic formula ID-1, where Rid is a saturated heterocyclic group. Each line in the table corresponds to five species which differ only at position Y. Following the table, representative species are presented by structural formula, and labeled with the corresponding Compound Number from the table. Compounds la-74d, 85a-86d, and 93a-94d are representative of compounds where G is phenyl; compounds 37a-38d, 77a-82d, 87a-92d, 95a-112d, and 115a-116d are representative of formula IA; compounds 127a-130d and 137a-142d are representative of formula II; compounds 113a-114d and 131a-136d of formula III; compounds 117a-124d of formula IV; and compounds 125a-126d of formula. V.
Table 5 Species of Generic Formulas ID-1, II-A and III-A
I I
Ari¨S¨NH X
or II H
Ar2 0 N 0 or Rid F
Ya,b,c, d, ore F
Ya = SCH3; Yb = Br; Y, = I; Yd = CI; Ye = CH3 Compound A = Rid, Ari, or Ar2 X
#
1 (a-e) phenyl Cl 2 (a-e) phenyl F
3 (a-e) 2-F-phenyl Cl 4 (a-e) 2-F-phenyl F
5 (a-e) 3 -F-phenyl Cl 6 (a-e) 3-F-phenyl F
7 (a-e) 4-F-phenyl Cl 8 (a-e) 4-F-phenyl F
9 (a-e) 2,4-di-F-phenyl Cl 10 (a-e) 2,4-di-F-phenyl F
11 (a-e) 2,5-di-F-phenyl Cl 12 (a-e) 2,5-di-F-phenyl F
13 (a-e) 2,6-di-F-phenyl Cl 14 (a-e) 2,6-di-F-phenyl F
(a-e) 3,4-di-F-phenyl Cl 16 (a-e) 3,4-di-F-phenyl F
17 (a-e) 3,5-di-F-phenyl Cl 18 (a-e) 3,5-di-F-phenyl F
19 (a-e) 2,6-di-F-phenyl Cl (a-e) 2,6-di-F-phenyl F
21 (a-e) 2,3,4-tri-F-phenyl Cl 22 (a-e) 2,3,4-tri-F-phenyl F
23 (a-e) 3,4,5-tri-F-phenyl Cl 24 (a-e) 3,4,5-tri-F-phenyl F
(a-e) penta-F-phenyl Cl 26 (a-e) penta-F-phenyl F
H
ClVfPD # A, A' B R
1 (a-d) H, H H 2-furanyl 2(a-d) H, H H 1,2,3 triazoly1-4-y1 3(a-d) H, H H 4-imidazoly1 4(a-d) H, H H 2-furanyl 5(a-d) H, H H 1,2,3 triazoly1-4-y1 6(a-d) H, H H 4-imidazoly1 7(a-d) H, H -CH2CH(OH)CH2OH 2-furanyl 8(a-d) H, H -CH2CH(OH)CH2OH
1,2,3 triazoly1-4-y1 9(a-d) H, H -CH2CH(OH)CH2OH 4-imidazoly1 10(a-d) -(CH2)2- -CH2(C3H5) 2-furanyl 11(a-d) -(CH2)2- -CH2(C3H5) 1,2,3 triazoly1-4-y1 12(a-d) -(CH2)2- -CH2(C31-15) 4-imidazoly1 13(a-d) -(CH2)2- CH3 4-thiazoly1 14(a-d) -(CH2)2- -CH2CH2OH 4-thiazoly1 15(a-d) -(CH2)2- -(CH2)2CH(OH)CH2OH
4-thiazoly1 16(a-d) CH3, H -(CH2)2CH(OH)CH2OH
4-thiazoly1 17(a-d) -(CH2)2- CH3 2-oxazoly1 18(a-d) -(CH2)2- -CH2CH2OH 2-oxazoly1 19(a-d) -(CH2)2- -(CH2)2CH(OH)CH2OH
2-oxazoly1 20(a-d) CH3, H -(CH2)2CH(OH)CH2OH
2-oxazoly1 Table 5 presents species of formulas II-A, and III-A, and also species of generic formula ID-1, where Rid is a saturated heterocyclic group. Each line in the table corresponds to five species which differ only at position Y. Following the table, representative species are presented by structural formula, and labeled with the corresponding Compound Number from the table. Compounds la-74d, 85a-86d, and 93a-94d are representative of compounds where G is phenyl; compounds 37a-38d, 77a-82d, 87a-92d, 95a-112d, and 115a-116d are representative of formula IA; compounds 127a-130d and 137a-142d are representative of formula II; compounds 113a-114d and 131a-136d of formula III; compounds 117a-124d of formula IV; and compounds 125a-126d of formula. V.
Table 5 Species of Generic Formulas ID-1, II-A and III-A
I I
Ari¨S¨NH X
or II H
Ar2 0 N 0 or Rid F
Ya,b,c, d, ore F
Ya = SCH3; Yb = Br; Y, = I; Yd = CI; Ye = CH3 Compound A = Rid, Ari, or Ar2 X
#
1 (a-e) phenyl Cl 2 (a-e) phenyl F
3 (a-e) 2-F-phenyl Cl 4 (a-e) 2-F-phenyl F
5 (a-e) 3 -F-phenyl Cl 6 (a-e) 3-F-phenyl F
7 (a-e) 4-F-phenyl Cl 8 (a-e) 4-F-phenyl F
9 (a-e) 2,4-di-F-phenyl Cl 10 (a-e) 2,4-di-F-phenyl F
11 (a-e) 2,5-di-F-phenyl Cl 12 (a-e) 2,5-di-F-phenyl F
13 (a-e) 2,6-di-F-phenyl Cl 14 (a-e) 2,6-di-F-phenyl F
(a-e) 3,4-di-F-phenyl Cl 16 (a-e) 3,4-di-F-phenyl F
17 (a-e) 3,5-di-F-phenyl Cl 18 (a-e) 3,5-di-F-phenyl F
19 (a-e) 2,6-di-F-phenyl Cl (a-e) 2,6-di-F-phenyl F
21 (a-e) 2,3,4-tri-F-phenyl Cl 22 (a-e) 2,3,4-tri-F-phenyl F
23 (a-e) 3,4,5-tri-F-phenyl Cl 24 (a-e) 3,4,5-tri-F-phenyl F
(a-e) penta-F-phenyl Cl 26 (a-e) penta-F-phenyl F
27 (a-e) 3 -C1-4-F-phenyl Cl
28 (a-e) 3-C1-4-F-phenyl F
29 (a-e) 2-CI-4-F-phenyl Cl (a-e) 2-CI-4-F-phenyl F
31 (a-e) 2-F-3 -C I-phenyl Cl Compound A = Rid, An, or Ar2 X
#
32 (a-e) 2-F-3-C1-phenyl F
33 (a-e) 2-F-4-CI-phenyl CI
34 (a-e) 2-F-4-CI-phenyl F
35 (a-e) 2-F-5-Cl-phenyl Cl 36 (a-e) 2-F-5-C1-phenyl F
37 (a-e) 3-cyano-4-F-phenyl Cl 38 (a-e) 3-cyano- 4-F-phenyl F
39 (a-e) 2-Cl-phenyl Cl 40 (a-e) 2-Cl-phenyl F
41 (a-e) 3-Cl-phenyl Cl , 42 (a-e) 3-Cl-phenyl F
43 (a-e) 4-Cl-phenyl Cl 44 (a-e) 4-Cl-phenyl F
45 (a-e) 2,3-di-Cl-phenyl Cl 46 (a-e) 2,3-di-Cl-phenyl F
47 (a-e) 2,5-di-Cl-phenyl Cl 48 (a-e) 2,5-di-Cl-phenyl F
49 (a-e) 2,6-di-Cl-phenyl Cl 50 (a-e) 2,6-di-Cl-phenyl F
51 (a-e) 3,5-di-Cl-phenyl Cl 52 (a-e) 3,5-di-Cl-phenyl F
53 (a-e) 2,4-di-Cl-phenyl Cl 54 (a-e) 2,4-di-Cl-phenyl F
55 (a-e) 3,4-di-Cl-phenyl Cl 56 (a-e) 3,4-di-Cl-phenyl F
57 (a-e) 2,4,6-tri-Cl-phenyl Cl 58 (a-e) 2,4,6-tri-Cl-phenyl F
59 (a-e) 2-C1-4-CF3-phenyl Cl 60 (a-e) 2-C1-4-CF3-phenyl F
61 (a-e) 2-CF3-phenyl Cl 62 (a-e) 2-CF3-phenyl F
63 (a-e) 3-CF3-phenyl Cl 64 (a-e) 3-CF3-phenyl F
65 (a-e) 4-CF3-phenyl Cl 66 (a-e) 4-CF3-phenyl F
67 (a-e) 2-CF30 phenyl Cl 68 (a-e) 2-CF30 phenyl F
69 (a-e) 3-CF30 phenyl Cl 70 (a-e) 3-CF30 phenyl F
71 (a-e) 4-CF30 phenyl Cl 72 (a-e) 4-CF30 phenyl F
73 (a-e) 4-CliF20-phenyl Cl 74 (a-e) 4-CHF20-phenyl F
75 (a-e) 2-methyl-5-nitro-phenyl Cl 76 (a-e) 2-methyl-5-nitro-phenyl F
77 (a-e) 2-cyano-phenyl Cl Compound A = Rid, Ari, or Ar2 X
78 (a-e) 2-cyano-phenyl 79 (a-e) 3 -cyano-phenyl Cl 80 (a-e) 3 -cyano-phenyl 81 (a-e) 4-cyano-phenyl Cl 82 (a-e) 4-cyano-phenyl 83 (a-e) 4-methoxy-phenyl Cl 84 (a-e) 4-methoxy-phenyl 85 (a-e) 3,4-dimethoxy-phenyl Cl 86 (a-e) 3,4-dimethoxy-phenyl 87 (a-e) 3-carbamyl-phenyl Cl 88 (a-e) 3-carbamyl-phenyl 89 (a-e) 3-carboxyl-phenyl Cl 90 (a-e) 3-carboxyl- phenyl 91 (a-e) 3-(N,N-dimethylcarbamoyl)phenyl Cl 92 (a-e) 3-(N,N-dimethylcarbamoyl)phenyl F
93 (a-e) 4-methylsulfonyl-phenyl Cl 94 (a-e) 4-methylsulfonyl-phenyl 95 (a-e) 3-(1,3,4 oxadiazol-2-yl)phenyl Cl 96 (a-e) 3-(1,3,4 oxadiazol-2-yl)phenyl 97 (a-e) 3-(1,3,4 thiadiazol-2-yl)phenyl Cl 98 (a-e) 3-(1,3,4 thiadiazol-2-yl)phenyl 99 (a-e) 3 -(5-methyl-1,3,4-oxadiazol)phenyl Cl 100 (a-e) 3-(5-methyl-1,3,4-oxadiazoOphenyl F
101 (a-e) 3-(5-methyl-1,3,4-thiadiazoOphenyl Cl 102 (a-e) 3-(5-methyl-1,3,4-thiadiazol)phenyl F
103 (a-e) 3 -am id inyl-phenyl Cl 104 (a-e) 3-am id inyl-phenyl 105 (a-e) 3 -(1H-tetrazolyl)phenyl Cl 106 (a-e) 3-(1H-tetrazolyl)phenyl 107 (a-e) 4-acetamido-phenyl Cl 108 (a-e) 4-acetamido-phenyl 109 (a-e) 3-C1-4-[(N-morpholinylcarbonyl) Cl amino]phenyl 110 (a-e) 3-C1-4-[(N-morpholinylcarbonyl) amino]phenyl 111 (a-e) 3-C1-4-[(N-pyrrolidinylcarbonyl) Cl amino]phenyl 112 (a-e) 3-C1-4- [(N-pyrro I idinylcarbonyl) amino]phenyl 113 (a-e) 3,5-dimethylisoxazoly1 Cl 114 (a-e) 3,5-dimethylisoxazoly1 115 (a-e) 4-(N-morpholinylsulfonyl)phenyl Cl 116 (a-e) 4-(N-morpholinylsulfonyl)phenyl 117 (a-e) 3-F-benzyl Cl 118 (a-e) 3-F-benzyl 119 (a-e) 4-F-benzyl Cl Compound A = Rub Ari, or Ar2 X
120 (a-e) 4-F-benzyl 121 (a-e) 3-F-phenyl-ethyl Cl .122 (a-e) 3-F-phenyl-ethyl 123 (a-e) 4-F-phenyl-ethyl Cl 124 (a-e) 4-F-phenyl-ethyl 125 (a-e) 8-quinolinyl Cl 126 (a-c) 8-quinolinyl 127 (a-e) 2-thienyl CI
128 (a-c) 2-thienyl 129 (a-e) 2,3-di-C1-thien-5-y1 Cl 130 (a-e) 2,3-di-C1-thien-5-y1 131 (a-e) 1,3,5 trimethy1-1H-pyrazoly1 Cl 132 (a-e) 1,3,5 trimethy1-1H-pyrazoly1 133 (a-e) 1,3-dimethy1-5-C1-1H-pyrazoly1 Cl 134 (a-e) 1,3-dimethy1-5-C1-1H-pyrazoly1 135 (a-e) 1-methy1-3-CF3-1H-pyrazol-4-y1 Cl 136 (a-c) 1-methy1-3-CF3-1H-pyrazol-4-y1 137 (a-e) 2-acetamido-4-methyl-thiazol-5-y1 Cl 138 (a-c) 2-acetamido-4-methyl-thiazol-5-y1 F
139 (a-c) 2,4-dimethyl-thiazol-5-y1 CI
140 (a-e) 2,4-dimethyl-thiazol-5-y1 141 (a-e) 1,2-dimethy1-1H-imidazol-4-y1 Cl 142 (a-c) 1,2-dimethy1-1H-imidazol-4-y1 Synthetic Procedures and Examples Compounds of this invention can be prepared by a variety of methods. The procedures below are intended to illustrate those methods, and the examples given are intended to illustrate the scope of this invention. Neither the methods not the examples should be construed as limiting the invention in any way.
I. The preparation of compound of formula VI is outlined below NO2 NO2 H x NH2 H x Ro 0 F Base RO 0 N,..
\1,1 reduction . Ro 40 n F y F F y F
F H2N,,../x F
I
jI III IV
Y
II (11 IPyridine protection R-1¨C1 or Et3N, CH2Cl2 0 v 0\ 0 0 0\ /0 H /2 R--S-,?
R =N
N--'( N¨\ H
, X N,,,,./X N X
Ro 0 Et3N, CH2C12 RO
.1 I
,. 0 Ro 1.1 j NaOH ' F
F y H F Y Y
F
R¨ F
R¨-Cl F
VII VIII VI
V
Scheme I above illustrates the preparation of sulfonamide derivatives of formula VI.
1,2 Diamine derivative (formula IV) can be easily prepared in two steps from the desired nitro derivatives (formula I). Compounds of formula IV can be reacted with the sulfonyl chloride derivatives (formula V, see next scheme) to form the desired sulfonamide.
Alternatively, the 1,2 diamine derivatives IV can be protected to for an imidazolidone (formula VII), before being reacted with the corresponding sulfonyl chloride.
Deprotection of the 1,2 diamine VIII under basic conditions provided the desired material VI.
II. The general route to synthesis compound of general formula V is outlined below R
CI n-BuOH t\ S 0 RBr ____________________ N 0Bu S 0Bu pyridine % n-BuLi ,.% %
IX )0( XI
R R
KSCN >LOK SOCl2 ., XII V
Scheme II above shows one example of the preparation of complex sulfonyl chloride.
Compound XX can be synthesized from IX, alkylated, and converted to the potassium salt XII. Treatment of the salt with SOC12 or POC13 affords the desired compounds.
Other more specific procedures to prepare unique sulfonyl chloride derivatives are reported in the experimental section.
The following examples are provided so that the invention might be more fully understood.
These examples are illustration of the scope of the invention only and should not be construed as limiting the invention in any way.
Typical procedures for the synthesis of sulfonamides:
Procedure A: To a solution of the amine (1 eq) in anhydrous dichloromethane (3 mL/
mmole) was added anhydrous triethylamine (5 eq). To this solution was added the sulfonyl chloride (1 eq) and the solution was stirred at room temperature for 16 h. The solvent was evaporated and the residue was purified by flash column chromatography on silica.
Procedure B: To a stirred solution of the amine (1 eq) in anhydrous pyridine (5m1/mmole) was added the sulfonyl chloride (1 - 5 eq). The reaction mixture was stirred at 40 C for 48 hours. The reaction mixture was partitioned with water and Et0Ac. The organic layer was washed with brine, dried (MgSO4) and concentrated under reduced pressure. The residue was purified by flash column chromatography on silica.
Example 1 N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)phenyl)methanesulfonamide:
Step A: 2,3-Difluoro-N-(2-fluoro-4-iodopheny1)-6-nitroaniline:
N (101 To a solution of 2-fluoro-4-iodoaniline (11.40 g, 47 mmol) in 100 ml anhydrous THF
at 0 C, 47 ml of a 1M solution of LHMDS in THF (47 mmol) was added dropwise.
The color of the solution turned dark purple. The solution was transferred via cannula to a dropping funnel, and the solution (containing the amine free base) was added in small portions to a solution of 2,3,4-trifluoronitrobenzene (8.321 g, 47.0 mmol) in anhydrous THF
(50 ml) at 0 'C. After completion of addition the mixture was stirred under argon at room temperature for 15 hours. The volume of the solvent was reduced, followed by extraction using ethyl acetate and brine. The organic layer was dried over sodium sulfate, the solvent was removed, and the obtained dark oil was purified by flash chromatography (Et0Ac /
hexane 1:5, Rf = 0.58) yielding the crude product, which became a brown solid upon drying in vacuo (yield: 6.23 g, 33.6%). m/z = 393 EM-if.
Step B: 5,6-Difluoro-N1-(2-fluoro-4-iodophenyl)benzene-1,2-diamine To a solution of nitro-diarylamine (6.23 g, 15.8 mmol) in 300 ml ethanol was added iron powder (13.74 g, 246 mmol) and ammonium chloride (13.59 g, 254 mmol) and the mixture was heated with stirring at 100 C oil bath temperature for 14 hours.
It was filtered and the residue washed two times with ethanol. The ethanol was removed in vacuo, and the residue was extracted using ethyl acetate / 1M NaOH solution. During the extraction, more precipitate was formed which was filtered and discarded. The combined organic layers were washed with brine and dried over sodium sulfate. The solvent was removed, and the crude product was recrystallized from CHC13 / hexane (1:50). The product was obtained as brown needles (2.094 g, 66%,). Rf = 0.44 (Et0Ac / Hex 1:3). 1H-NMR (500 MHz, CDC13):
5 = 7.40-7.38 (dd, 1H, J= 11.3 Hz, J= 1.5 Hz). 7.25-7.23 (d, 1H, J= 8.5 Hz), 6.97-6.92 (q, 1H, J= 9 Hz), 6.51-6.48 (m, 1H), 6.24-6.21 (t, 1H, J= 9 Hz), 5.3 (s, 1H, NH, br), 3.80 (s, 2H, NI-12, br); LRMS (ESI): nilz = 365 [M+Hr.
Step C: N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino) phenyl) methanesulfonamide:
0// 1\11-1 H F
N
OI
According to the general procedure A, 5,6-difluoro-N1-(2-fluoro-4-iodophenyl)benzene-1,2-diamine was reacted with methanesulfonyl chloride to obtain the desired product. 1HNMR: (500 MHz, CDC13): 8 = 7.38-7.37 (d, 111), 7.35-7.34 (m, 1H), 7.27-7.26 (m, 1H), 7.20-7.0 (q, 1H), 6.68 (s, 1H, br), 6.15-6.12 (q, 1H), 5.65 (s, 1H, br), 2.95 (s, 3H); in/z= 441 [M-11".
Example 2 N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)phenyl)cyclopropanesulfonamide:
N
According to the general procedure A, 5,6-difluoro-N1-(2-fluoro-4-iodophenyl) benzene-1,2-diamine was reacted with cyclopropanesulfonyl chloride to obtain the desired product. 1HNMR.: (500 MHz, CDC13): 8 = 7.38-7.37 (d, 1H), 7.35-7.34 (m, 1H), 7.27-7.26 (m, 1H), 7.20-7.0 (q, 1H), 6.68 (s, 1H, br), 6.15-6.12 (q, 1H), 5.65 (s, 1H, br), 3.25-3.20 (m, 1H), 2.4-2.3 (m, 2H), 2.0-1.8 (m, 2H); in/z = 467 [M-lf.
Example 3 N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)phenyl)propane-2-sulfonamide:
)s(,0 0/ 1µ1F1 El F
F I
F
According to the general procedure A, 5,6-difluoro-N1-(2-fluoro-4-iodophenyl)benzene-1,2-diamine was reacted with isopropylsulfonyl chloride to obtain the desired product. Yield: 39%. 1H-NMR (500 MHz, CDC13): 5 = 7.50-7.43 (m, 1H), 7.35-7.34 (m, 1H), 7.27-7.26 (m, 1H), 7.15-7.09 (q, 1H, J= 1.6 Hz), 6.62 (s, 1H, br), 6.22-6.18 (q, 1H, J= 1.5 Hz), 5.65 (s, 1H, br), 3.30-3.28 (in, 1H), 1.38-1.37 (d, 6H, J= 1.2 Hz); m/z = 469 [M-IT.
Example 4 N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)phenyl)butane-l-sulfonamide:
Fi F
F I
F
According to the general procedure A, 5,6-difluoro-N1-(2-fluoro-4-iodophenyl)benzene-1,2-diamine was reacted with n-butylsulfonyl chloride to obtain the desired product. Yield: 55%. 1H-NM (500 MHz, CDC13): 6 = 7.50-7.43 (in, 1H), 7.35-7.34 (m, 1H), 7.27-7.26 (m, 1H), 7.15-7.09 (q, 1H, J= 1.6 Hz), 6.62 (s, 1H, br), 6.22-6.18 (q, 1H, J= 1.5 Hz), 5.65 (s, 1H, br), 3.06-3.031 (t, 2H, J= 1.4 Hz), 1.75-1.71 (m, 2H), 1.38-1.36 (m, 2H), 0.87-0.86 (t, 3H, J= 1.3 Hz); rn/z = 483 [M-lf.
Example 5 N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)pheny1)-2,2,2-trifluoro ethane sulfonamide:
F3C,S(/
cy 'NH H F
N
According to the general procedure A, 5,6-difluoro-N1-(2-fluoro-4-iodophenyl)benzene-1,2-diamine was reacted with 1,1,1-trifluoroethylsulfonyl chloride to obtain the desired product. Yield: 28%. tn/z = 509 [M-lf.
Example 6 N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)phenyl)butane-2-sulfonamide:
s(/0 e 'NH H F
According to the general procedure A, 5,6-difluoro-N1-(2-fluoro-4-iodophenyl)benzene-1,2-diamine was reacted with sec-butylsulfonyl chloride to obtain the desired product. Yield: 22%. 1H-NMR (500 MHz, Me0H[d4]): 5 = 7.60-7.40 (m, 3H), 7.18-7.00 (q, 1H), 6.55-6.45 (m, 1H), 3.55-3.50 (m, 1H), 2.20-2.00 (m, 1H), 1.80-1.60 (m, 111), 1.43-1.40 (d, 3H), 1.06-1.04 (t. 3H); tn/z = 483 [m-if.
Example 7 N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)pheny1)-N-methyl cyclopropane sulfonamide:
ACo 'N H F
N
To a solution of N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)phenyl)cyclopropane-sulfonamide (see Example 2) (283.9 mg, 0.61 mmol) in 3 ml anhydrous THF was added at -78 C a 1M solution of LHMDS (0.6 ml, 0.6 mol) and the solution was stirred for 10 min at this temperature. Then, methyl iodide (0.8 ml, 1.824 g, 12.9 mmol) was added and the mixture was warmed to room temperature and stirred for 7 h. The solvent was removed and the residue extracted using EtAc and brine. The organic fractions were dried using Na2SO4 and the solvent was removed. The obtained crude product was purified using flash-column chromatography (Si, EtAc/Hexanes 1:2, Rf = 0.45). Yield: 205 mg, 70%). 1H-NMR (500 MHz, CDC13): 5 =
7.41-7.39 (d, 1H, J = 10 Hz), 7.30-7.29 (d, 1H, J = 8.0 Hz), 7.23-7.20 (m, 1H), 6.98-6.93 (q, 1H, J = 8.5 Hz), 6.60 (s, 1H, br), 6.51-6.47 (m, 1H), 3.23 (s, 3H), 2.46-2.42 (m, 1H), 1.19-1.16 (m, 2H), 1.04-1.02 (m, 2H); in/z¨ 481 [M-lf.
Example 8 1-Chloro-N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)phenyl) methane sulfonamide:
CI
cy NH Ei F
N
According to the general procedure A, 5,6-difluoro-N1-(2-fluoro-4-iodophenyl)benzene-1,2-diamine was reacted with chloromethanesulfonyl chloride to obtain the desired product. m/z = 475 rm-ir.
Example 9 N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)pheny1)-2-methylpropane-2-sulfonamide:
g ll'NH H F
=
la F I
F
According to the general procedure B, 5,6-difluoro-N1-(2-fluoro-4-iodophenyl)benzene-1,2-diamine was reacted with 2-methylpropane-2-sulfonyl chloride 5 (synthesized according to the literature procedure) to obtain the desired product. 1H NMR
(300 MHz, CDC13): 6 7.50 (m, 1H), 7.43 (dd, J= 1.8 & 10.5 Hz, 1H), 7.28 (br s, 1H), 7.10 (dd, J= 9.0 & 17.7 Hz, 1H), 6.48 (br s, D20 exchangeable, 1H), 6.19 (t, J= 7.8 & 9.6 Hz, 1H), 5.58 (br s, D20 exchangeable, 1H), 1.39 (s, 9H); m/z = 383 [M-lf.
10 Example 10 N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)phenyl)cyclopentanesulfonamide:
V, 0-- 8 NH Ed F
'FOP
F
According to the general procedure B, 5,6-difluoro-N1-(2-fluoro-4-iodophenyl)benzene-1,2-diamine was reacted with cyclopentanesulfonyl chloride to obtain the desired product1H NMR (300 MHz, CDC13): 6 7.42 (dd, J= 2.1 & 10.5 Hz, 1H), 7.36 (ddd, J= 2.4, 4.8, & 9.3 Hz, 1H), 7.25 (m, 2H), 7.10 (dd, J= 9.6 & 17.7 Hz, 1H), 6.67 (br s, D20 exchangeable, 1H), 6.20 (dt, J= 1.5, 8.4 & 17.4 Hz, 1H), 3.53 (p, 1H), 1.80 (m, 8H); m/z = 495 EM-if.
Example 11 N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)phenyl)cyclohexanesulfonamide:
H
0s, ,8 NH id F
lei lel F I
F
According to the general procedure B, 5,6-difluoro-N1-(2-fluoro-4-iodophenyObenzene-1,2-diamine was reacted with cyclohexanesulfonyl chloride to obtain the desired product. 1HNMR (300 MHz, CDC13): 5 7.43 (dd, J=1.5 & 10.2 Hz, 1H), 7.37 (ddd, J= 2.4, 4.8 & 9.6 Hz, 1H), 7.27 (m, 111), 7.11 (dd, J= 9.3 & 18.0 Hz, 1H), 6.64 (br s, 1H), 6.18 (dt, J= 1.5, 9.0 & 17.4 Hz, 1H), 5.63 (br s, 1H), 2.95 (triplet of triplet, 2.10-1.16 (m, 10H); rn/z = 509 [M-lf.
Example 12 N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)pheny1)-1-methylcyclopropane-1-sulfonamide:
Step A: n-Butyl 3-chloro-1-propanesulfonate:
CIS'C) o' 0-nBu Triethylamine (28 ml, 200 mmol) in CH2C12 (50 ml) was slowly added to an ice-cooled solution of 3-chloro-1-propanesulfonyl chloride (36.6g, 200 mmol) and 1-butanol (18.4 g, 240 m mol) in CH2C12 (250 ml) and stirring was continued for 16h. The mixture was diluted with CH2C12 (200 ml), washed (aqueous HC1) and dried (MgSO4) and the solvent was evaporated to obtain the titled product 1 (40.85 g, 95%) in crude form as slightly yellow oil which was used for the next reaction without further purification. III NMR
(CDC13)) 5 0.94 (t, J = 7.5 Hz, 3H), 1.44 (sextet, 2H), 1.72 (quintet, 2H), 2.31(quintet, 2H), 3.27(t, J = 6.9 Hz, 2H), 3.68 (t, J = 6.3 Hz), 4.23 (t, J = 6.6 Hz, 2H).
Step B: 1-Butyl cyclopropanesulfonate:
so 0-nBu Solutions of 1-butyl 3-chloro-1-propanesulfonate (4.6 g, 21.39 mmol in 25 ml THF) and of butyllithium (14.7 ml, 23.53 mmol, 1.6M, THF) were simultaneously added to THF
(150 ml) at -78 C under nitrogen atmosphere. The solution was allowed to warm to 0 C and then quenched with water (2 m1). The volatiles evaporated under reduced pressure and the residue extracted with CH2C12 (150 m1). The extract was washed with water and dried (MgSO4) and evaporated to give crude desired product (3.23 g, 78.22%) in almost pure form as pale yellow oil which was used for next step without further purification.
1H NMR (300 MHz, CDC13) 6 0.94 (t, J = 7.5 Hz, 3H), 1.07 (m, 2H), 1.25 (m, 2H), 1.45(sextet, 2H), 1.74(quintet, 2H), 2.45 (heptet, 1H), 4.23 (t, J = 6.6 Hz, 2H).
Step C: Butyl 1-Methyl-cyclopropanesulfonate:
'6"Q, O'Y-0-nBu To a solution of 1-Butyl cyclopropanesulfonate (1 g, 5.58 mmol) in THF (15 ml) butyllithium solution ( 3.84 ml, 6,14 mmol, 1.6M, THF) was slowly added at -78 C under nitrogen atmosphere. After 15 minutes Mel (0.72 ml, 11.16 mmol) was added and the solution was allowed to warm to 0 C and quenched with water (1 m1). The volatiles evaporated under reduced pressure and the residue extracted with CH2C12 (100 m1). The extract was washed with water, dried (MgSO4) and evaporated. The residue was purified over silica gel chromatography (eluants: hexane/ CH2C12) to obtain the titled product (0.59 g, 55.0%) as a colorless oil. 1H NMR (300 MHz, CDC13)) 6 0.84 (m, 2H), 0.95 (t, J
= 7.2 Hz, 3H), 1.43 (m, 4H), 1.53 (s, 3H), 1.74(m, 2H), 4.21 ((t, J = 6.6 Hz, 2H).
Step D: 1-Potassium 1-Methyl-cyclopropanesulfonate:
OK
A mixture of 1- Butyl 1-Methyl-cyclopropanesulfonate (0.386 g, 2 mmol) and potassium thiocyanate (0.194 g, 2 mmol) in DME (5 ml) and water (5 ml) was refluxed for 16h. The volatiles were evaporated to obtain the crude sulfonate (0.348g, quantitative) which was dried under vacuum at 50 C for 16h. The crude product was used in the next reaction without further purification. NMR (300 MHz, D20) 5 0.56 (t, J = 6.3 Hz, 2H), 0.96 (t, J =
6.3 Hz, 2H), 1.26 (s, 3H).
Step E: 1-Methyl-cyclopropanesulfonylchloride:
CI
A solution of 1-potassium 1-methyl-cyclopropanesulfonate (0.348 g, 2 mmol), thionyl chloride (5 ml) and DMF (5 drops) was refluxed at 60 C for 16h. The volatiles evaporated under reduced pressure and the residue extracted with CH2C12 (50 m1). The extract was washed with water, dried (MgSO4) and evaporated to obtain the crude product as yellow gummy oil which was used in the next reaction without further purification.
Step F: N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)pheny1)-1-methylcyclopropane-1-sulfonamide:
_II 'NH H F
la lel According to the general procedure B, 5,6-difluoro-N1-(2-fluoro-4-iodophenyl)benzene-1,2-diamine was reacted with 1-methyl-cyclopropanesulfonylchloride to obtain the desired product. 1H NMR (300 MHz, CDC13): 8 7.42 (dd, J= 1.8 & 10.5 Hz, 1H), 7.36 (ddd, J= 2.4, 4.5 & 9.0 Hz, 1H), 7.27 (d, J= 6.0 Hz, 1H), 7.07 (dd, J=
9.3 & 17.7 Hz, 1H), 6.24 (dt, J= 2.1, 8.7 & 17.4 Hz, 1H), 5.86 (br s, 1H), 1.43 (s, 3H), 1.33 (t, J= 5.4 Hz, 2H), 0.75 (dd, J= 5.1 & 6.3 Hz, 2H); m/z = 481 {M-lf.
Example 13 N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)pheny1)-1-(2,3-dihydroxypropyl) cyclopropane-l-sulfonamide:
Step A: Butyl cyclopropanesulfonate:
Aõ.
sO
Cyclopropanesulfonyl chloride (5 g, 35 mmole, 1 eq) was dissolved in an excess BuOH (20 ml), the reaction mixture was cooled at -10 C and pyridine (5.8 mL, 70 mmole, 2 eq) was slowly added dropwise. The mixture was slowly warmed at room temperature and stirred overnight. The solvent was removed under reduced pressure and the resulting white solid was dissolved in CHC13. The organic phase was washed with water, brine and dried (MgSO4) and concentrated to give an oil (4.8 g, 24.9 mmole, 71%). 1HNMR (300 MHz, CDC13): 8 4.25 (t, 2H), 2.46 (m, 1H), 1.74 (m, 2H), 1.45 (m, 2H), 1.25 (dd, 2H), 1.09 (dd, 2H), .93 (t, 3H).
Step B: Butyl 1-allylcyclopropane-1-sulfonate:
r, To a solution of 1-butyl cyclopropanesulfonate (4.8 g, 24.9 mmole) in THF at -78 C was added simultaneously butyllithium solution (15. 6 ml, 24.9 mmol, 1.6M, THF) and ally!
iodide (24.9 mmole) under nitrogen atmosphere. The reaction mixture was stirred 2 hours at -78 C and 3 hours at room tempoerature. The volatiles were evaporated under reduced pressure and the residue extracted with CH2C12 (100 m1). The extract was washed with water, dried (MgSO4) and evaporated. The residue was purified over silica gel chromatography (eluants: hexane/ CH2C12) to obtain the titled product (3.75 g, 69.0%) as a colorless oil. Ili NMR (300 MHz, CDCI3): 5 5.6 (m, 1H), 5.13-5.08 (t, 2H), 4.21 (t, 2H), 2.65 (d, 2H), 1.7 (m, 2H), 1.4 (in, 4H), .93 (m, 5H).
Step C: Potassium 1-allylcyclopropane-1-sulfonate:
AlrO-K+
S, d/ \O
A mixture of 1- butyl 1-methyl-cyclopropanesulfonate (3.75 g, 17.2 mmol) and potassium thiocyanate (1.7 g, 17.2 mmol) in DME (20 ml) and water (20 ml) was refluxed for 16h. The volatiles were evaporated to obtain the crude sulfonate (3.44g, quantitative) which was dried under vacuum at 50 C for 16h. The crude product was used in the next reaction without further purification. 1H NMR (CDC13): 5 5.6 (m, 1H), 4.91-4.85 (dd, 2H), 2.471-2.397 (d, 2H), 0.756 (m, 2H), 0.322 (m, 2H).
Step D: 1-allylcyclopropane-1-sulfonyl chloride:
LKICI
S
0/' A solution of potassium 1-allylcyclopropane-1-sulfonate (3.44 g, 17.2 mmol), thionyl chloride (10 ml) and DMF (5 drops) was refluxed at 60 C for 16h. The volatiles evaporated under reduced pressure and the residue extracted with CH2C12 (50 m1). The extract was washed with water, dried (MgSO4) and evaporated to obtain the crude product as yellow gummy oil which was washed with hexane and used in the next reaction without further purification (2.7 g, 15 mmole, 87%). 111 NMR (300 MHz, CDC13): 5 5.728 (m, 1H), 5.191 (t, 2H), 2.9 (d, 2H), 0.756 (m, 2H), 0.322 (m, 2H).
Step E: 1-allyl-N-(3,4-difluoro-2-(2-fluoro-4-iodophenvlamino)phenyl)cyclopropane-1-sulfonamide:
FOI
According to the general procedure B, 5,6-difluoro-N1-(2-fluoro-4-iodophenyl)benzene-1,2-diamine was reacted with 1-allylcyclopropane-1-sulfonyl chloride to obtain the desired product. m/z = 507 [M-ir.
Step F: N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)pheny1)-1-(2,3-dihydroxypropyl)cyclopropane-1-sulfonamide:
õ31,15q HO
H'NH H F
1-Allyl-N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino) phenyl)cyclopropane-1-sulfonamide ( 0,77 g, 1.52 mmole) and 4-methylmorpholine N-oxide (0,18 g, 1.52 mmole) were dissolved in THF (50 mL). Osmium tetroxide was added at room temperature (0.152 mmole, 0.965 mL, 4% in H20) and the reaction mixture was stirred at room temperature for 16 hours. Et0Ac was added, the organic phase was washed with water, dried (MgSO4) and concentrated under reduced pressure. The residue was purified over silica gel chromatography (eluants: Et0Ac/ Me0H) to obtain the titled product (0. 65 g, 79%). Ili NMR (300 MHz, CDC13 + D20): 8 7.38 (dd, J= 1.8 & 10.5 Hz, 1H), 7.36 (ddd, J=
2.4, 5.1 & 9.3 Hz, 1H), 7.25 (d, J= 8.7 Hz, 1H), 7.02 (dd, J= 9.0 & 17.7 Hz, 1H), 6.27 (dt, J= 3.0, 8.7 & 17.4 Hz, 1H), 3.92 (m, 1H), 3.54 (dd, J= 3.9 & 11.1 Hz, 1H), 3.39 (dd, J= 6.6 & 11.1 Hz, 1H), 2.16 (dd, J= 9.6 & 15.9 Hz, 1H), 1.59 (d, J= 14.1 Hz, 1H), 1.41 (m, 1H), 1.26 (m, 1H), 0.83 (m, 2H); m/z = 542 [M-1]..
Example 14 (S)-N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)pheny1)-1-(2,3-dihydroxypropyl)cyclopropane-1-sulfonamide:
HO
NH H F
The pure S isomer was obtained by chiral HPLC separation of the racemic mixture (example 13). 'H NMR (300 MHz, CDC13+ D20): 8 7.38 (dd, J= 1.8 & 10.5 Hz, 1H), 7.36 (ddd, J= 2.4, 5.1 & 9.3 Hz, 1H), 7.25 (d, J= 8.7 Hz, 1H), 7.02 (dd, J= 9.0 &
17.7 Hz, 1H), 6.27 (dt, J= 3.0, 8.7 & 17.4 Hz, 1H), 3.92 (m, 1H), 3.54 (dd, J= 3.9 & 11.1 Hz, 1H), 3.39 (dd, J= 6.6 & 11.1 Hz, 1H), 2.16 (dd, J= 9.6 & 15.9 Hz, 1H), 1.59 (d, J= 14.1 Hz, 1H), 1.41 (m, 1H), 1.26 (m, 1H), 0.83 (m, 2H); m/z = 542 D.4-1f.
Example 15 (R)-N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)pheny1)-1-(2,3-dihydroxypropyl)cyclopropane-1-sulfonamide:
OH v-7 1-1'NH H F
1.1 The pure R isomer was obtained by chiral HPLC separation of the racemic mixture (example 13). IH NMR (300 MHz, CDC13 + D20): 67.38 (dd, J= 1.8 & 10.5 Hz, 1H), 7.36 (ddd, J= 2.4, 5.1 & 9.3 Hz, 1H), 7.25 (d, J= 8.7 Hz, 1H), 7.02 (dd, J= 9.0 &
17.7 Hz, 1H), 6.27 (dt, J= 3.0, 8.7 & 17.4 Hz, 1H), 3.92 (m, 1H), 3.54 (dd, J= 3.9 & 11.1 Hz, 1H), 3.39 (dd, J= 6.6 & 11.1 Hz, 1H), 2.16 (dd, J= 9.6 & 15.9 Hz, 1H), 1.59 (d, J= 14.1 Hz, 1H), 1.41 (m, 1H), 1.26 (m, 1H), 0.83 (m, 2H); nilz = 542 [M-lf.
Example 16 N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)pheny1)-1-(2-hydroxyethyl)cyclopropane-l-sulfonamide:
Step A: 2-(1-bromocyclopropyl)ethanol:
Br OH
To a solution of neat diethyl zinc (3.3 ml, 3.977 g, 30 mmol) in 100 ml anhydrous DCM was added very slowly trifluoroacetic acid (2.31 ml, 3.4188 g, 30 mmol) dropwise at 0 C. (Caution: Violent gas evolution, exothermic!). After completed addition of the TFA, the suspension was stirred for 20 min at the same temperature, followed by the addition of diiodo methane (2.45 ml, 8.134 g, 30.4 mmol). It was further stirred at 0 C for 20 min, and then a solution of 3-bromobut-3-en-1-ol (1 ml, 1.523 g, 10.1 mmol) in 10 ml DCM was added at the same temperature. After complete addition, the mixture was warmed to room temperature and stirred for 4 hours. The mixture was quenched with 100 ml Me0H and 40 ml brine, and it was further stirred for 30 min. The solvents were reduced, and the residue extracted using CHC13 / aq. NH4C1. The organic layers were collected, washed with brine and water, and the solvent was removed to give 2-(1-bromocyclopropy1)-ethanol in sufficient purity (1.6564 g, 100%). 1H-NMR (500 MHz, CDCI3): 8 = 3.90-3.83 (t, 2H), 1.91-1.87 (t, 2H), 1.71 (s, 1H, br), 1.14-1.09 (m, 2H), 0.83-0.79 (m, 2H).
Step B: TBS protected 2-(1-bromocyclopropyl)ethanol:
Br OTBS
To a solution of the cyclopropyl alcohol (Step A) (1.303 g, 7.95 mmol) in 30 ml anhydrous DCM was added anhydrous pyridine (1.2 ml, 1,1736 g, 14.8 mmol) and TBSOTf (2.7 ml, 3.1077 g, 11.76 mol) and the solution was stirred at room temperature for 16 h. It was extracted with CHCI3 / brine and the organic fraction was dried with MgSO4. The solvent was reduced and the crude product purified using flash-column chromatography (Si, CHC13 /
hexanes 1:10, Rf 0.4). Yield: 0.796 g, 36%. 'H-NMR (500 MHz, CDC13): 8 = 3.95-3.75 (t, 2H), 1.95-1.85 (t, 2H), 1.15-1.05 (m, 2H), 0.95-0.80 (m, 11H), 0.15-0.05 (s, 6H).
Step C: TBS protected 2-(1-chlorosulfonylcyclopropyl)ethanol:
OTBS
To a solution of the cyclopropyl bromide prepared in step B (1.1227 g, 4.04 mmol) in ml anhydrous diethyl ether was added a 1.7 M solution of t-BuLi in pentane (4.8 ml, 8.16 15 mmol) at ¨ 78 C. The solution was stirred for 30 min at this temperature, and was then transferred via a transfer canola into a solution of freshly distilled sulfuryl chloride (0.65 ml, 1.029 g, 8.1 mmol) in 8 ml diethyl ether at ¨ 78 C. The yellow suspension was warmed to room temperature. The solvent was removed, and the residue was dried in vacuo to remove excessive sulfuryl chloride. Then, the residue was extracted two times with hexane, and after filtration the solvent was evaporated in vacuo to give the sulfonyl chloride in sufficient purity as a colorless oil. Yield: 870 mg (72%). 1H-NMR (300 MHz, CDC13): 6 = 3.95-3.85 (t, 2H), 2.35-2.25 (t, 2H), 1.80-1.70 (m, 2H), 1.45-1.38 (m, 2H), 0.90 (s, 9H), 0.10 (s, 6H).
Step D: TBS-protected N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)pheny1)-1-(2-hydroxyethyl)cyclopropane-l-sulfonamide:
(OTBS
N
OI
According to the general procedure B, 5,6-difluoro-N1-(2-fluoro-4-iodophenyl)benzene-1,2-diamine was reacted with the cyclpropylsulfonyl chloride prepared in step C to obtain the desired product. 1H-NMR (300 MHz, CDC13): 5 = 7.44-7.39 (dd, 1H), 7.32-7.24 (m, 2H), 7.1-6.98 (q, 1H), 6.34-6.24 (m, 1H), 6.16 (s, 1H, br), 3.85-3.75 (t, 2H), 2.15-2.00 (t, 2H), 1.35-1.20 (m, 2H), 0.95-0.75 (m, 11H), 0.10 (s, 6H); in/z = 625 [Mir.
Step E: N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)pheny1)-1-(2-hydroxyethyl)cyclopropane-l-sulfonamide:
(OH
Alk/e0 cy NH H F
N
To a solution of the TBS-protected sulfonamide prepared in step D (21 mg, 0.033 mmol) in 1 ml THF was added 0.1 ml aq.1.2N HC1 solution at 0 C and the solution was stirred for 2 h.
The solvents were reduced and the residue was extracted using aq. NaHCO3 solution and EtAc.
The organic fractions were dried with MgSO4 and the volatiles were removed.
The crude product was purified using flash-column chromatography (Si, CHC13 / Me0H 10:1, R, = 0.45) to give the pure product. Yield: 16.9 mg (100%). 1H-NMR (300 MHz, CDCI3): 5 =
7.44-7.39 (dd, 1H), 7.32-7.24 (m, 2H), 7.1-6.98 (q, 1H), 6.34-6.24 (m, 1H), 6.16 (s, 1H, br), 3.85-3.75 (t, 2H), 2.15-2.00 (t, 2H), 1.35-1.20 (m, 2H), 0.95-0.85 (m, 2H); m/z = 511 [M-lf.
Example 17 N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)pheny1)-3-hydroxypropane-1-sulfonamide:
II
HO (3 NH H F
To a solution of 3-Chloro-N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)pheny1)-propane-1-sulfonamide (69.4 mg, 0.138 mmol) in a mixture of 8 ml 1,4-dioxane and 2 ml H20 was added KOH powder (0.674 g, 12.0 mmol) and the mixture was heated to the reflux temperature for 3 days. It was extracted using EtAc / brine, the organic fraction was dried with Na2SO4 and 10 the volatiles were removed. The residue was purified using flash-column chromatography (Si, DCM / Me0H 5:1, Rf = 0.3). Yield: 41 mg (62%). 1H-NMR (500 MHz, Me0H [d4]): 6 = 7.38-7.21 (d, 1H), 7.23-7.21 (d, 1H), 7.06-7.00 (q, 1H), 6.52-6.50 (m, 1H). 6.17-6.13 (t, 1H), 3.30-3.27 (t, 2H), 2.86-2.83 (t, 2H), 2.05-2.00 (m, 2H); m/z = 485 [m-if.
Example 18 N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)pheny1)-2-methyl-5-(trifluoromethyl)furan-3-sulfonamide:
1;) 0'NH
According to the general procedure 5,6-difluoro-N1-(2-fluoro-4-iodophenyl)benzene-1,2-diamine (0.182 mmole) was reacted with 2-methyl-5-(trifluoromethyl)furan-3-sulfonyl chloride (0.5 mmole) to form N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)pheny1)-2-methyl-5-(trifluoromethyl)furan-3-sulfonamide. 1H NMR (CDC13) 5 2.2 (s, 3H), 5.3 (s, 1H), 6.0 (dt, 1H), 6.8 (s, 114), 6.95 (s, 1H), 7.0-7.3 (m, 3H), 7.4 (dd, 1H).
Example 19 N-(5-(N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)phenyl)sulfamoy1)-methylthiazol-2-yl)acetamide:
HN
0'NH
la 40 According to the general procedure 5,6-difluoro-N1-(2-fluoro-4-iodophenyObenzene-1,2-diamine (0.182 mmole) was reacted with 2-acetamido-4-methylthiazole-5-sulfonyl chloride (0.5 mmole) to obtain N-(5-(N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)phenypsulfamoy1)-4-methylthiazol-2-ypacetamide . 1H NMR
(CDC13)) 2.1 (s, 3H), 2.2 (s, 3H), 5.9 (dt, 1H), 6.05 (s, 1H), 7.0-7.6 (m, 3H), 7.4 (dd, 1H), 8.0 (s, 1H).
Example 20 5-(5-Chloro-1,2,4-thiadiazol-3-y1)-N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino) phenyl) thiophene-2-sulfonamide:
CI
o N
0'NH
According to the general procedure 5,6-difluoro-N1-(2-fluoro-4-iodophenyl)benzene-1,2-diamine (0.182 mmole) was reacted with 5-(5-chloro-1,2,4-thiadiazol-3-yl)thiophene-2-sulfonyl chloride (0.5 mmole) to obtain 5-(5-chloro-1,2,4-thiadiazol-3-y1)-N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)phenyl)thiophene-2-sulfonamide. 1H NMR (300 MHz, CDC13)) 8 5.8 (dt, 1H), 5.95 (s, 1H), 6.95 (d, 1H),7.4 (m, 2H), 7.6 (d, 1H), 7.8 (s, 1H).
Example 21 N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)pheny1)-3,5dimethylisoxazole-4-sulfonamide:
N, ?
OX--\
0'NH
According to the general procedure 5,6-difluoro-N1-(2-fluoro-4-iodophenyl) benzene-1,2-diamine (0.182 mmole) was reacted with 3,5-dimethylisoxazole-4-sulfonyl chloride (0.5 mmole) to obtain N-(3,4-difluoro-2-(2-fluoro-4-iodophenyl amino)pheny1)-3,5dimethylisoxazole-4-sulfonamide. 1H NMR (300 MHz, CDC13)) 8 2.2 (s, 3H), 2.4 (s, 3H), 5.8 (s, 1H), 6.0 (dt, 1H), 5.95 (s, 111), 6.9 (s, 1H),7.0 (q, 1H), 7.2 (m, 3H), 7.4 (dd, 1H).
Example 22 5-Chloro-N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)pheny1)-1,3-dimethyl-1H-pyrazole-4-sulfonamide:
Nõ
Si According to the general procedure 5,6-difluoro-N1-(2-fluoro-4-iodophenyl) benzene-1,2-diamine (0.182 mmole) was reacted with 5-chloro-1,3-dimethy1-1H-pyrazole-4-sulfonyl chloride (0.5 mmole) to obtain 5-chloro-N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino) phenyl)-1,3-dimethy1-1H-pyrazole-4-sulfonamide. 1H NM-R (300 MHz, CDC13)) 5 2.1 (s, 3H), 3.6 (s, 3H), 5.8 (s, 1H), 5.95 (dt, 1H), 7.0 (q, 1H), 7.2 (d, 1H),7.3 (m, 2H), 7.4 (dd, 1H).
Example 23 N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)pheny1)-2,5-dimethylfuran-3-sulfonamide:
0,.....--0'NH F
H
N
lei 110 F I
F
According to the general procedure 5,6-difluoro-N1-(2-fluoro-4-iodophenyl) benzene-1,2-diamine (0.182 mmole) was reacted with 2,5-dimethylfuran-3-sulfonyl chloride (0.5 mmole) to obtain N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino) pheny1)-2,5-dimethylfuran-3-sulfonamide. 1H NMR (300 MHz, CDC13)) 8 2.2 (s, 3H), 2.3 (s, 3H), 5.8 (s, 1H), 6.0 (dt, 1H), 6.8 (s, 1H), 7.0 (q, 1H), 7.2 (d, 1H),7.3 (m, 2H), 7.4 (dd, 1H).
Example 24 N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)pheny1)-1-methy1-3-(trifluoromethyl)-1H-pyrazole-4-sulfonamide:
NI,Ni..
F3C-yIC:
H
N
Si la F I
F
According to the general procedure 5,6-difluoro-N1-(2-fluoro-4-iodophenyl) benzene-1,2-diamine (0.182 mmole) was reacted with 1-methy1-3-(trifluoromethyl)-1H-pyrazole-4-sulfonyl chloride (0.5 mmole) to obtain N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)pheny1)-1-methy1-3-(trifluoromethyl)-1H-pyrazole-4-sulfonamide. 1H
NMR (300 MHz, CDCI3)) 6 3.8 (s, 3H), 5.7 (s, 1H), 6.0 (dt, 1H), 7.0 (q, 1H), 7.2 (m, 2H), 7.4 (dd, 1H),7.8 (s, 1H).
Example 25 N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)pheny1)-2,4-dimethylthiazole-5-sulfonamide:
S)N
CO"---0..SNH F
H
N
F I
F
According to the general procedure 5,6-difluoro-N1-(2-fluoro-4-iodophenyl) benzene-1,2-diamine (0.182 mmole) was reacted with 2,4-dimethylthiazole-5-sulfonyl chloride (0.5 mmole) to obtain N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)phenyI)-2,4-dimethylthiazole-5-sulfonamide. 111 NMR (300 MHz, CDC13)) 6 2.3 (s, 3H), 2.6 (s, 3H), 5.7 (s, 1H), 5.9 (dt, 1H), 7.1 (q, 1H), 7.2 (d, 1H), 7.3 (m, 1H),7.4 (d, 1H), 7.4 (s, 111).
Example 26 N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)pheny1)-1,2-dimethy1-1H-imidazole-4-sulfonamide:
N\
1:Dr N
According to the general procedure B, 5,6-difluoro-N1-(2-fluoro-4-iodophenyObenzene-1,2-diamine was reacted with 1,2-dimethy1-1H-imidazole-4-sulfonyl chloride to obtain the title compound. 1H NMR. (300 MHz, CDC13): 6 7.95 (br s, 1H), 7.37 (dd, J= 1.8 & 10.8 Hz, 1H), 7.32-7.14 (m, 3H), 6.98 (dd, J= 9.6 & 17.7 Hz, 1H), 5.87 (dt, J
= 4.2, 9.0 & 17.4 Hz, 1H), 5.55 (br s, 1H), 3.49 (s, 3H), 2.31 (s, 3H).
Example 27 N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)phenyl)thiophene-3-sulfonamide:
g, S ONO
According to the general procedure B, 5,6-difluoro-N1-(2-fluoro-4-iodophenyl) benzene-1,2-diamine was reacted with thiophene-3-sulfonyl chloride to obtain the title compound. 1H NMR (300 MHz, CDC13): 6 8.00 (dd, J= 1.2 & 3.3 Hz, 1H), 7.45 (dd, J= 0.9 & 5.1 Hz, 1H), 7.35 (m, 2H), 7.27 (m, 2H), 6.91 (dd, J= 9.3 & 17.1 Hz, 1H), 6.64 (ddd, J=
2.1, 4.8 & 8.7 Hz, 1H), 6.34 (dt, J= 5.4, 8.7 & 14.1 Hz, 1H), 5.98 (br d, J=
2.1 Hz, D20 exchangeable, 1H).
Example 28 N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)phenyl)furan-2-sulfonamide:
According to the general procedure B, 5,6-difluoro-N1-(2-fluoro-4-iodophenyl)benzene-1,2-diamine was reacted with furan-2-sulfonyl chloride to obtain the title 5 compound. 1H NMR (300 MHz, CDC13): 8 7.53 (br s, D20 exchangeable, 1H), 7.38 (dd, J-1.8 & 10.5 Hz, 1H), 7.30 (d, J= 8.4 Hz, 1H), 7.21 (d, J= 3.0 Hz, 1H), 6.96 (dd, J= 8.7 &
16.5 Hz, 1H), 6.87 (ddd, J= 1.8, 5.1 & 9.0 Hz, 1H), 6.53 (dd, J= 1.8 & 3.6 Hz, 1H), 6.44 (dt, J= 5.1, 8.7 & 13.8 Hz, 1H), 6.22 (br s, D20 exchangeable, 1H).
10 Example 29 N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)pheny1)-5-methylthiophene-2-sulfonamide:
s s.
NH Fd F
According to the general procedure B, 5,6-difluoro-N1-(2-fluoro-4-iodophenyl)benzene-1,2-diamine was reacted with 5-methylthiophene-2-sulfonyl chloride to obtain the title compound. 1HNMR (300 MHz, CDC13): 8 7.34 (dd, .1= 0.9 & 10.2 Hz, 1H), 7.30 (ddd, J= 2.1, 4.8 & 9.0 Hz, 1H), 7.25 (d, J= 3.9 Hz, 1H), 7.07 (m, 2H), 6.65 (dd, J=
1.2 & 3.9 Hz, 1H), 5.89 (dt, J= 2.4, 8.7 & 17.4 Hz, 1H), 5.54 (br s, D20 exchangeable, 1H), 2.46 (s, 3H).
Example 30 5-Chloro-N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)phenyl)thiophene-2-sulfonamide:
S NH N F
\ / 0 H
According to the general procedure B, 5,6-difluoro-N1-(2-fluoro-4-iodophenyl)benzene1,2-diamine was reacted with 5-chlorothiophene-2-sulfonyl chloride to 5 obtain the title compound. 1H NMR (300 MHz, CDC13): 6 7.38 (dd, J=1.5 &
10.2 Hz, 1H), 7.32 (ddd, J= 2.1, 5.1 & 9.3 Hz, 1H), 7.25 (d, J= 3.9 Hz, 1H), 7.10 (dd, J=
9.0 & 18.6 Hz, 3H), 6.84 (d, J= 4.2 Hz, 1H), 5.86 (dt, J= 1.8, 8.7 & 17.4 Hz, 1H), 5.49 (br s, D20 exchangeable, 1H).
Example 31 5-Bromo-N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)phenyl)thiophene-2-sulfonamide:
SNH N F
\ / 0 H
According to the general procedure B, 5,6-difluoro-N1-(2-fluoro-4-iodophenyObenzene1,2-diamine was reacted with 5-bromothiophene-2-sulfonyl chloride to obtain the title compound. 1HNMR (300 MHz, CDC13): 6 7.39-7.29 (m, 2H), 7.20-7.05 (m, 3H), 6.96 (d, J= 3.6 Hz, 1H), 5.85(dt, J= 2.1, 9.0 & 17.4 Hz, 1H), 5.54 (br s, 1H).
Example 32 4-Bromo-N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)phenyl)thiophene-3-sulfonamide:
&(gl, / II NH
According to the general procedure B, 5,6-difluoro-N1-(2-fluoro-4-iodophenyObenzene1,2-diamine was reacted with 4-bromothiophene-3-sulfonyl chloride to obtain the title compound. 11-1NMR (300 MHz, CDC13): 8 7.48 (br m, 2H), 7.39 (dd, J= 1.8 & 10.5 Hz, 1H), 7.28 (ddd, J= 2.4, 4.8 & 9.0 Hz, 111), 7.17 (d, J= 8.4 Hz, 111), 7.02 (m, 1H), 6.02 (dt, J= 2.4, 8.7 & 17.4 Hz, 1H), 5.68 (br s, 1H).
Example 33 4-Bromo-5-chloro-N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)phenyl)thiophene-2-sulfonamide:
H F
Br According to the general procedure B, 5,6-difluoro-N1-(2-fluoro-4-iodophenyl)benzene1,2-diamine was reacted with 4-bromo-5-chlorothiophene-2-sulfonyl chloride to obtain the title compound. 1HNMR (300 MHz, CDC13): 8 7.42-7.34 (m, 2H), 7.25 (br m, 3H), 7.13 (dd, J= 9.0 & 17.1 Hz, 1H), 6.02 (dt, J= 2.4, 6.6 & 17.4 Hz, 1H), 5.52 (br s, 1H).
Example 34 3-Bromo-5-ehloro-N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino) phenyl)thiophene-2-sulfonamide:
CI s H F
Br 40 According to the general procedure B, 5,6-difluoro-N1-(2-fluoro-4-iodophenyl)benzene1,2-diamine was reacted with 3-bromo-5-chlorothiophene-2-sulfonyl chloride to obtain the title compound. 'H NMR (300 MHz, CDC13): 6 7.41 (dd, J=
2.1 & 10.5 Hz, 111), 7.35 (br m, 2H), 7.31 (dd, J= 2.1 & 4.2 Hz, 1H), 7.19 (d, J= 8.7 Hz, 1H), 7.08 (dd, J= 9.0 & 17.4 Hz, 1H), 6.02(dt, J= 2.1, 8.4 & 17.1 Hz, 1H), 5.59 (br s, 1H).
Example 35 N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)pheny1)-2,5-dimethylthiophene-3-sulfonamide:
N7S.
s 8 NH F
According to the general procedure B, 5,6-difluoro-N1-(2-fluoro-4-iodophenyl)benzene1,2-diamine was reacted with 2,5-dimethylthiophene-3-sulfonyl chloride to obtain the title compound. 1H NMR (300 MHz, CDC13): 6 7.39 (dd, J= 1.8 &
10.2 Hz, 1H), 7.24-7.16 (br m, 2H), 7.13 (dd, J= 9.0 & 17.4 Hz, 1H), 6.77 (d, J= 9.6 Hz, 1H), 5.98 (dt, J= 2.4, 8.7 & 17.4 Hz, 11-1), 5.55 (br s, 1H), 2.33 (s, 6H).
Example 36 2,5-Diehloro-N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)phenyl)thiophene-3-sulfonamide:
S ? / 8 NH H F
F I
F
According to the general procedure B, 5,6-difluoro-N1-(2-fluoro-4-iodophenyl)benzene1,2-diamine was reacted with 2,5-dichlorothiophene-3-sulfonyl chloride to obtain the title compound. 1HNMR (300 MHz, CDC13): 8 7.41(dd, J=1.5 & 10.5 Hz, 1H), 7.28-7.20 (m, 2H), 7.08 (dd, J= 9.0 & 17.4 Hz, 2H), 6.99 (s, 1H), 6.03 (dt, J=
2.1, 8.7 &
17.4 Hz, 1H), 5.56 (br s, 1H).
Example 37 Methyl 3-(N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)phenyl) sulfamoyl)thiophene-2-carboxylate:
sia/I.NH Fd F
Me02C 40 1110 F I
F
According to the general procedure B, 5,6-difluoro-N1-(2-fluoro-4-iodophenyl) benzene1,2-diamine was reacted with methyl 3-(chlorosulfonyl)thiophene-2-carboxylate to obtain the title compound. 1HNMR (300 MHz, CDC13): 8 8.58 (s, 1H), 7.43 (dd, J=5.1&
10.8 Hz, 2H), 7.35 (dd, J= 1.8 & 10.2 Hz, 1H), 7.31 (ddd, J= 2.1, 4.2 & 9.3 Hz, 1H), 7.04 (m, 2H), 5.88 (dt, J= 2.7, 8.7 & 17.4 Hz, 1H), 5.65 (br s, 1H), 3.85 (s, 3H).
Example 38 Methyl 5-(N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)phenyl)sulfamoy1)-1-methyl-1H-pyrrole-2-carboxylate:
yH, 9 Me02CO3 k N H'NH
According to the general procedure B, 5,6-difluoro-N1-(2-fluoro-4-iodophenyl)benzene1,2-diamine was reacted with methyl 5-(chlorosulfony1)-1-methy1-1H-pyrrole-2-carboxylate to obtain the title compound. 1HNMR (300 MHz, CDC13): 6 7.37 (dd, J= 1.8 & 10.5 Hz, 1H), 7.29 (m, 2H), 7.12-6.94 (m, 4H), 5.87 (dt, J= 1.8, 8.4 & 17.4 Hz, 1H), 5.56 (br s, 1H), 3.65 (s, 3H), 3.75 (s, 3H).
Example 39 N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)pheny1)-5-methylisoxazole-4-sulfonamide:
II NH H F
SFOI
According to the general procedure A, 5,6-difluoro-N1-(2-fluoro-4-iodophenyl)benzene1,2-diamine was reacted with the corresponding sulfonyl chloride to obtain the title compound.
Yield: 22%. m/z = 508 [MAI.
Example 40 3-Chloro-N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)phenyl)propane-1-sulfonamide:
CI
0 i\11-1 H F
According to the general procedure A, 5,6-difluoro-N1-(2-fluoro-4-iodophenyl)benzene-1,2-diamine was reacted with 3-chloropropane-1-sulfonyl chloride to obtain the desired product. 114 NMR (500 MHz, CDC13): 8 = 7.39-7.38 (d, 1H), 7.35-7.34 (m, 1H), 7.27-7.26 (m, 1H), 7.10-7.0 (q, 1H), 6.63 (s, 1H, br), 6.15-6.11 (q, 1H), 5.60 (s, 1H, br), 3.60-3.56 (t, 2H), 3.22-3.20 (m, 2H), 2.22-2.16 (m, 2H).
General procedure C: Synthesis of N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)pheny1)-2-(alkylamino)ethanesulfonamide:
2-Chloro-ethanesulfonyl chloride (0.1 ml, 1 mmol) was added to a solution of 5,6-difluoro-N1-(2-fluoro-4-iodophenyObenzene-1,2-diamine (0.364 g, 1 mmol) and triethylamine (0.28 ml, 2 mmol) in CH2Cl2 (5 ml) and the reaction mixture was stirred at room temperature for 16h. Then it's treated with an excess amine (10 eq) either in solution or as a neat liquid. The reaction mixture stirred at room temperature for additional 6h. The reaction mixture diluted with CH2C12 (10 ml) and water (10 m1). The organic layer was sequentially washed with dil.
HC1(2x20 ml, 2N) and saturated NaHCO3 (2x10 ml) solution. Then the CH2C12 layer dried (MgSO4) and evaporated to obtain the crude product. The impure product was purified under preparative HPLC conditions to obtain the pure products in 50-60 % yield.
Example 41 N-(2-(4-chloro-2-fluorophenylamino)-3,4-difluorophenyl) cyclopropanesulfonamide:
0'NH
N
CI
See example 1. 1H NMR (300 MHz, CDC13) 60.85-0.95 (m, 2H), 1.05-1.15 (m, 2H), 2.2-2.4 (m, 1H), 5.8 (s, 1H), 6.3 (t, 1H), 6.6-7.4 (m, 5H); m/z = 375 [M-lf.
Example 42 N-(3,4-difluoro-2-(4-iodo-2-methylphenylamino)phenyl)cyclopropanesulfonamide:
oy See example 1. IH NMR (CDC13) 60.80-1.0 (m, 211), 1.05-1.20 (m, 211), 1.55 (s, 311), 2.4-2.5 (m, 1H), 5.6 (s, 1H), 6.2 (dd, 1H), 6.4 (s, 111), 7.1 (q, 1H). 7.3-7.4 (m, 211), 7.5 (s, 1H); m/z = 463 {m-if.
Example 43 N-(2-(4-tert-butyl-2-chlorophenylamino)-3,4-difluorophenyl) cyclopropanesulfonamide:
oy See example 1. 1}INMR (300 MHz, CDC13) 60.9-1.0 (m, 211), 1.05-1.20 (m, 2H), 1.3 (s, 9H), 2.4-2.5 (m, 1H), 5.8 (s, 1H), 6.3 (dd, 1H), 6.6 (s, 111), 7.0-7.2 (m, 2H), 7.3-7.4 (m, 211); m/z= 413 [M-l].
Example 44 N-(2-(2,4-dichlorophenylamino)-3,4-difluorophenyl)cyclopropanesulfonamide:
oy CI
See example 1. 111NMR (300 MHz, CDCI3) 8 0.9-1.0 (m, 2H), 1.05-1.20 (m, 2H), 2.4-2.5 (m, 1H), 6.0 (s, 1H), 6.3 (dd, 111), 6.6 (s, 1H), 7.0-7.2 (m, 2H), 7.3-7.4 (m, 2H); m/z =
392 [M-lf.
Example 45 3-Chloro-N-(3,4-difluoro-2-(2-fluoro-4-trifluoromethyl) phenylamino)phenyl)propane-1-sulfonamide:
H NH H F
See example 1.1H NMR (300 MHz, CDC13): 67.39-7.26 (m, 2H), 7.25 (m, 1H), 7.18 (dd, J= 9.0 & 17.7 Hz, 1H), 6.78 (br s, D20 exchangeable, 1H), 6.50 (t, J= 8.1 Hz, 1H), 6.00 (br d, D20 exchangeable, J= 1.5 Hz, 1H), 3.63 (t, J= 6.0 & 6.3 Hz, 211), 3.29 (t, J= 7.2 &
7.8 Hz, 2H), 2.26 (quintet, 2H); m/z = 445 [M-lf.
Example 46 N-(3,4-difluoro-2-(2-chloro-4-trifluoromethyl)phenylamino)methanesulfonamide:
s, NH H CI
N
See example 1.1H NMR (300 MHz, CDC13): 8 7.65 (d, J=7.8 Hz, 111), 7.33 (m, 211), 7.19 (dd, J= 9.3 & 17.4 Hz, 111), 6.90 (br s, D20 exchangeable, 1H), 6.45 (dd, J=1.5 & 8.4 Hz, 111), 6.39 (br s, D20 exchangeable, 1H), 3.02 (s, 3H); in/z = 399 [M-lf.
Example 47 3-Chloro-N-(3,4-difluoro-2-(2-chloro-4-trifluorom ethyl) phenylamino)phenyl)propane-1-sulfonamide:
H CI
N
See example 1.1H NMR (300 MHz, CDCI3): 5 7.66 (d, J= 1.5 Hz, 1H), 7.36 (m, 2H), 7.19 (dd, J= 9.0 & 17.4 Hz, 1H), 6.91 (br s, D20 exchangeable, 11-1), 6.50 (dd, J= 8.4 & 1.5 Hz, 1H), 6.37 (s, D20 exchangeable, 1H), 3.62 (t, J= 6.0 Hz, 2H), 3.29 (t, J=7.5 & 7.8 Hz, 2H), 2.27 (quintet, 2H); in/z = 462 [M-lf.
Example 48 3-Chloro-N-(3,4-difluoro-2-(2-bromo-4-trifluoromethyl) phenylamino)phenyl)propane-1-sulfonamide:
rt NH H Br N
See example 1.1H NMR (300 MHz, CDCI3): 8 7.82 (s, 1H), 7.38 (m, 2H), 7.20 (dd, J
= 9.0 & 17.7 Hz, 1H), 6.62 (br s, D20 exchangeable, 1H), 6.43 (d, J= 8.4 Hz, 1H), 6.23 (s, D20 exchangeable, 1H), 3.65 (t, J= 6.0 Hz, 2H), 3.30 (t, J= 7.5 Hz, 2H), 2.28 (quintet, 2H);
m/z = 506 [M-1T.
Example 49 Cyclopropanesulfonic acid (3,4,6-trifluoro-2-(2-fluoro-4-iodo-phenylamino)-phenyl)-amide:
Step A (2-Fluoro-4-iodo-phenyl)-(2,3,5-trifluoro-6-nitro-phenyp-amine:
F I
F
A stirred solution of 2-fluoro-4-iodoaniline (3.64 gm, 15.37 mmol) in dry THE' (100 ml) under nitrogen was cooled to -78 C and a solution of 1.0 M lithium hexa methyl disilazide (LiN(SiMe3)2) "LHMDS" (15.37 ml, 15.37 mmol) was added slowly. This reaction mixture was kept stirring at -78 C for another hour and then 2,3,4,6-tetrafluoronitrobenzene was added. The reaction mixture was allowed to warm to room temperature and stirring continued for another 16 hours. Ethyl acetate (200 ml) was added to the reaction mixture and was washed with water. Organic layer was dried over sodium sulfate and further purified by column chromatography to provide yellow solid (3.75 gm, yield: 59.24%). M-H+:
410.9.111 NMR (DMSO, 300 MHz): 6.85 (t, 1H); 7.38 (d, 1H); 7.62 (m, 2H); 8.78 (s, 1H).
Step B 3,4,6-Trifluoro-N2-(2-Fluoro-4-iodo-phenyl)-benzene-1,2-diamine:
F I
F
To the stirred solution of (2-fluoro-4-iodo-pheny1)-(2,3,5-trifluoro-6-nitro-pheny1)-amine 3 (5.2 gm, 12.62 mmol) in Et0H (200 ml), ammonium chloride (10.12 gm, 189.3 mmol) and iron powder (10.57 gm, 189.3 mmol) was added. This reaction mixture was kept stirring at reflux for 16 hours. Reaction mixture was allowed to cool and was filtered over celite and concentrated to dryness. The residue obtained was taken into Et0Ac and was washed with water. The Et0Ac layer was dried over sodium sulfate and further purified by crystallization from Et0H to provide off-white solid (3.2 gm, yield: 66.39%).
M-H+: 381.1.
1H NMR (DMSO, 300 MHz): 5.0 (s, 2H); 6.2 (t, 1H); 7,2 - 7.3 (m, 2H); 7.45 (s, 1H); 7.5 (d, 1H).
Step C: 4,6,7-Trifluoro-1-(2-Fluoro-4-iodo-pheny1)-1,3,-dihydrobenzoimidazole-one:
H, P
N--`( F N
To the stirred solution of 3,4,6-trifluoro-N2-(2-Fluoro-4-iodo-pheny1)-benzene-1,2-diamine 3 (0.285 gm, 0.74 mmol) in CH2C12 (2 ml), 1,1'-carbonyldiimidazole (0.125 gm, 0.75 mmol) was added. This reaction mixture was kept stirring at room temperature for 16 hours when product precipitated out. The white solid was filtered and used further without any purification. (0.2 gm, yield: 65.85%); m/z = 407 [M-1]-.
Step DIE: Cyclopropanesulfonic acid (3,4,6-trifluoro-2-(2-fluoro-4-iodo-phenylamino)-pheny1)-amide:
0õ
F lel N 1110 A stirred solution of 4,6,7-trifluoro-1-(2-fluoro-4-iodo-pheny1)-1,3,-dihydrobenzimidazol-2-one (0.2 gm, 0.41 mmol) in dry THF (4 ml) under nitrogen was cooled to -78 C and a solution of 1.0 M LiHMDS (0.41 ml, 0.41 mmol) was added slowly. (2 ml) followed by addition of cyclopropanesulfonyl chloride (0.050 ml, 0.49 mmol). This reaction mixture was kept stirring at room temperature for 16 hours, concentrated to dryness and was taken into Et0Ac. The Et0Ac was washed with water, dried over sodium sulfate and concentrated to dryness. The residue obtained 1-cyclopropanesulfony1-4,5,7-trifluoro-3-(2-fluoro-4-iodo-pheny1)-1,3-dihydro-benzimidazol-2-one 5 was taken into dioxane (2 ml) and to this 1.0 N NaOH (0.5m1) was added and kept stirring at room 50 C for 16 hours. TLC
indicated incomplete reaction, the product was purified by HPLC to provide off-white solid (4.4 mg) M+H+: 484.7, M-le: 486.7.1H NMR (CDC13, 300 MHz): 0.9 ¨ 1.1 (m, 2H);
1.1 -1.2 (in, 2H); 2.45 ¨2.55 (m, 1H); 6.05 (s, 1H); 6.44 ¨ 6.54 (m, 1 H); 7.1 (s, 1H); 7.4 ¨ 7.7 (d, 1H); 7.38 ¨ 7.44 (dd, 1H); ni/z = 485 [M-lf.
Example 50 N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)-6-ethoxyphenyl)cyclopropane sulfonamide:
Step A: (2,3-Difluoro-5-methoxy-6-nitro-pheny1)-(2-fluoro-4-iodo-pheny1)-amine:
Me N
A stirred solution of (2-fluoro-4-iodo-phenyl)-(2,3,5-trifluoro-6-nitro-pheny1)-amine (1.23 gm, 3 mmol) in dry THF (25 ml) under nitrogen was cooled to -78 C and a solution of 25% Na0Me (0.68 ml, 0.3 mmol) was added slowly. Reaction mixture was allowed to warm to room temperature and stirring continued for another 16 hours. TLC indicated incomplete reaction. Ethyl acetate (100 ml) was added to the reaction mixture and was washed with water. Organic layer was dried over sodium sulfate and further purified by column chromatography to provide yellow solid (0.6 gm, yield: 47.6%). m/z = 424 [M=H1-Step B: 5,6-Difluoro-N1-(2-fluoro-4-iodopheny1)-3-methoxybenzene-1,2-diamine:
Me0 N
To the stirred solution of (2,3-difluoro-5-methoxy-6-nitro-phenyl)-(2-fluoro-4-iodo-phenyl)-amine (0.57 gm, 1.34 mmol) in Et0H (20 ml), ammonium chloride (1.18 gm, 20.16 mmol) and iron powder (1.15 gm, 21.44 mmol) was added. This reaction mixture was kept stirring at reflux for 16 hours. Reaction mixture was allowed to cool and was filtered over celite and concentrated to dryness. The residue obtained was taken into Et0Ac and was washed with water. The Et0Ac layer was dried over sodium sulfate and further purified by crystallization from Et0H to provide off-white solid (0.47 gm, yield: 90.3%).
M-H+: 393.2.
1H NMR (DMSO, 300 MHz): 3.76 (s, 3H); 6.1 (t, 1H); 6.8 - 7.0 (m, 1H); 7.2 (d, 1H); 7.35 (s, 1H); 7.42 (d, 1H).
Step C: 6,7-Difluoro-1-(2-fluoro-4-iodopheny1)-4-methoxy-1H-benzo[d]imidazol-2(3H)-one:
H p Me0 N
To the stirred solution of 5,6-difluoro-N1-(2-fluoro-4-iodopheny1)-3-methoxybenzene-1,2-diamine (0.17 gm, 0.43 mmol) in CH2Cl2 (2 ml), 1,1'-Carbonyldiimidazole (0.085 gm, 0.53 mmol) was added. This reaction mixture was kept stirring at room temperature for 16 hours when product precipitated out. The white solid was filtered and used further without any purification. (0.089 gm); m/z = 419 [M-1].
Step fl/F: N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)-6-methoxyphenyl) cyclopropanesulfonamide:
,0 H
Me0 N
A stirred solution of 1-(cyclopropylsulfony1)-4,5-difluoro-3-(2-fluoro-4-iodopheny1)-7-methoxy-1H-benzo[djimidazol-2(3H)-one (0.89 gm, 0.17 mmol) in dry THF (4 ml) under nitrogen was cooled to -78 C and a solution of 1.0 M LiHMDS (0.17 ml, 0.17 mmol) was added slowly. (2 ml) followed by addition of Cyclopropanesulfonyl chloride (0.021 ml, 0.21 mmol). This reaction mixture was kept stirring at room temperature for 16 hours, concentrated to dryness and was taken into Et0Ac. The Et0Ac was washed with water, dried over sodium sulfate and concentrated to dryness. The resulting 1-(cyclopropylsulfony1)-4,5-difluoro-3-(2-fluoro-4-iodopheny1)-7-methoxy-1H-benzo[d]imidazol-2(3H)-one was taken into dioxane (2 ml) and to this 1.0 N NaOH (0.5m1) was added and kept stirring at room 50 C
for 16 hours. TLC indicated incomplete reaction, the product was purified by HPLC to provide off-white solid (2.5 mg) M+H+: 484.7, M-H+: 497.3. 11-1 NMR (CDC13, 300 MHz):
0.85 ¨0.95 (m, 2H); 1.05 ¨1.15 (m, 2H); 2.4 ¨ 2.5 (m, 1H); 3.9 (s, 3H); 6.1 (s, 1H); 6.4 ¨ 6.6 (m, 2 H); 7.3 (m, 1H); 7.35 ¨ 7.4 (dd, 111); m/z = 497 [-m-if.
Example 51 Methylsulfonic acid (3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-6-methoxy-pheny1)-amide:
$0 I
0sNH
Me0 N
A stirred solution of 5,6-difluoro-N1-(4-fluoro-2-iodopheny1)-3-methoxybenzene-1,2-diamine (0.150 gm, 0.38 mmol) in dry CH2C12 (4 ml), TEA (.264 ml, 1.9 mmol) and Methanesulfonyl chloride was added slowly. This reaction mixture was kept stirring at room temperature for 16 hours, TLC indicated incomplete reaction along with starting material two products were observed. The reaction mixture was washed with water, organic layer was dried over sodium sulfate and concentrated to dryness. the product was purified by column chromatography. The minor product was found to be the expected compound (6.4 mg). M-H+: 471.5. 1H NMR (CDC13, 300 MHz): 3.9 (s, 3H); 6.05 (s, 1H); 6.4 ¨ 6.5 (m, 11-1'); 6.5 ¨6.6 (m, 1H); 7.2 (s, 1H); 7.28 (d, 1H); 7.35 ¨ 7.4 (d, 1H); m/z = 471 pvi-ir.
Example 52 1-(2,3-Dihydroxy-propyI)-cyclopropanesulfonic acid [3,4,6-trifluoro-2-(2-fluoro-4-iodo-phenylamino)-phenyll-amide:
Step A: 1-Allyl-cyclopropanesulfonic acid [3,4,6-trifluoro-2-(2-fluoro-4-iodo-phenylamino)-phenyl]-amide:
II 'NH H F
5 According to the general procedure B, 1-allyl-cyclopropanesulfonyl chloride was reacted with 3,5,6-trifluoro-N1-(2-fluoro-4-iodophenyl)benzene-1,2-diamine to obtain the title product. 114 NMR (CDC13, 300 MHz): 5 7.41 (dd, 1H), 7.38 (dd, 1H), 7.09 (s, 1H), 6.78 (m, 1H), 6.49 (m, 1H), 5.96 (s, 1H), 5.86 (m, 1H), 5.18 (d, 2H), 2.76 (d, 2H), 1.23 (m, 2H), 0.872 (m, 2H).
Step B: 1-(2,3-Dihydroxypropy1)-N-(3,4,6-trifluoro-2-(2-fluoro-4-iodophenylamino) phenyl)cyclopropane-l-sulfonamide:
HO
n'NH H F
1-Allyl-cyclopropanesulfonic acid [3,4,6-trifluoro-2-(2-fluoro-4-iodo-phenyl amino)-phenyl]-amide ( 110 mg, 0.21 mmole) and 4-methylmorpholine N-oxide (24.6 mg, 0.21 mmole) was dissolved in TIE (8 mL). Osmium tetroxide was added at room temperature (0.021 mmole, 0.153 mL, 4% in H20) and the reaction mixture was stirred at room temperature for 16 hours. Et0Ac was added, the organic phase was washed with water, dried (MgSO4) and concentrated under reduced pressure. The residue was purified over silica gel chromatography (eluants: Et0Ac/ Me0H) to obtain the titled product (0. 89 g, 75 %). 1H
NMR (CDC13, 300 MHz): 5 7.39 (dd, J = 1.5 & 10.6 Hz, 1H), 7.29 (d, J = 8.8 Hz, 1H), 7.28 (s, 1H), 6.97 (s, 1H), 6.76 (m, 1H), 6.49 (m, 111), 4.13 (m, 1H), 3.66 (dd, J
= 3.7 & 11.4 Hz, 1H), 3.53 (dd. J = 6.7 & 112 Hz, 1H), 2.50(dd, J = 10,0 & 16.1 Hz, 1H), 1.6 (m,1H), 1.46 (m, 1H), 1.28 (m, 1H), 1.20 (m, 2H), 0.92 (m, 2H); in/z = 559 Example 53 (S)-1-(2,3-dihydroxypropy1)-N-(3,4,6-trifluoro-2-(2-fluoro-4-iodophenylamino) phenyl)cyclopropane-1-sulfonamide:
NH HO
H F
The pure S isomer was obtained by chiral HPLC separation of the racemic mixture (example 52). 1H NMR (CDC13, 300 MHz): 8 7.39 (dd, J = 1.5 & 10.6 Hz, 111), 7.29 (d, J =-8.8 Hz, 1H), 7.28 (s, 1H), 6.97 (s, 1H), 6.76 (m, 1H), 6.49 (m, 1H), 4.13 (m, 1H), 3.66 (dd, J
= 3.7 & 11.4 Hz, 1H), 3.53 (dd. J'= 6.7 & 11.2 Hz, 1H), 2.50(dd, J= 10.0 &
16.1 Hz, 1H), 1.6 (m,1H), 1.46 (m, 1H), 1.28 (m, 1H), 1.20 (m, 2H), 0.92 (m, 2H); m/z = 559 [M-ir.
Example 54 (R)-1-(2,3-dihydroxypropy1)-N-(3,4,6-trifluoro-2-(2-fluoro-4-iodophenylamino) phenypcyclopropane-1-sulfonamide:
Ho,F,A1 Tr NH H F
The pure R isomer was obtained by chiral HPLC separation of the racemic mixture (example 52).1H NMR (CDC13, 300 MHz): 5 7.39 (dd, J = 1.5 & 10.6 Hz, 11-1), 7.29 (d, J =
8.8 Hz, 1H), 7.28 (s, 1H), 6.97 (s, 111), 6.76 (m, 1H), 6.49 (m, 1H), 4.13 (m, 1H), 3.66 (dd, J
= 3.7& 11.4 Hz, 1H),3.53 (dd. J = 6.7 & 11.2 Hz, 1H), 2.50(dd, J = 10.0& 16.1 Hz, IH), 1.6 (m,1H), 1.46 (m, 1H), 1.28 (m, 111), 1.20 (m, 2H), 0.92 (m, 211); tn/z =
559 [M-11".
Example 55 N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)-6-methoxypheny1)-1-(2,3-dihydroxypropypeyclopropane-1-sulfonamide:
Step A: 1-Allyl-N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)-6-methoxyphenyOcyclopropane-l-sulfonamide p NH H F
I
Me0 According to the general procedure B, 1-allyl-cyclopropanesulfonyl chloride was reacted with 5,6-difluoro-N1-(2-fluoro-4-iodopheny1)-3-methoxybenzene-1,2-diamine to obtain the title product. 1HNMR (CDC13, 300 MHz): 8 7.417 (dd, 1H), 7.309(s, 111), 7.25 (m, 111), 6.89 (m, 111), 6.52(m, 1H), 6.427 (m, 111), 6.03 (s,1H), 5.668 (m, 111), 5.11 (t, 1H), 3.9 (s, 3H), 2.75 (d, 2H), 1.21 (m, 2H), 0.767 (m, 211).
Step B: N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)-6-methoxypheny1)-1-(2,3-dihydroxypropyl)cyclopropane-1-sulfonamide HO
NH H F
Me0 la 1-Allyl-N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)-6-methoxyphenyl) cyclopropane-1 -sulfonamide ( 97 mg, 0.18 mmole) and 4-methylmorpholine N-oxide (21 mg, 0.18 mmole) were dissolved in TIM (8 mL). Osmium tetroxide was added at room temperature (0.018 mmole, 0.13 mL, 4% in H20) and the reaction mixture was stirred at room temperature for 16 hours. Et0Ac was added, the organic phase was washed with water, dried (MgSO4) and concentrated under reduced pressure. The residue was purified over silica gel chromatography (eluants: Et0Ac/ Me0H) to obtain the titled product (0. 80 g, 78 %). 1H
NMR (CDC13, 300 MHz): 5 7.38 (dd, J = 1.7 & 10.3 Hz,1H), 7.26 (m, 1H), 7.14 (s, 1H), 6.87 (s, 1H), 6.53 (dd, J = 6.8 & 11.4 Hz, 1H), 6.43 (m, 1H), 4.06 (m, 1H), 3.89 (s, 3H), 3.63 (dd, J = 3.7 & 11.1 Hz, 1H), 3.49 (dd, J = 6.4 & 11.1 Hz, 1H), 2.3 (dd, J =
9.7 & 16.1 Hz, 1H), 1.77 (dd, J = 1.9 & 16.0 Hz, 1H), 1.37 (m, 1H), 1.25 (m, 111), 1.21 (m, 2H), 0.86 (m, 2H); m/z = 571 [M-1]..
Example 56 (S)-N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)-6-methovpheny1)-1-(2,3-dihydroxypropyl)cyclopropane-l-sulfonamide:
5;5) HO
NH H F
Me0 The pure S isomer was obtained by chiral HPLC separation of the racemic mixture (example 55).1H NMR (CDC13, 300 MHz): 5 7.38 (dd, J = 1.7 & 10.3 Hz,1H), 7.26 (m, 111), 7.14 (s, 1H), 6.87 (s, 1H), 6.53 (dd, J = 6.8 & 11.4 Hz, 1H), 6.43 (m, 1H), 4.06 (m, 1H), 3.89 (s, 3H), 3.63 (dd, J = 3.7 & 11.1 Hz, 1H), 3.49 (dd, 3= 6.4 & 11.1 Hz, 1H), 2.3 (dd, J = 9.7 &
16.1 Hz, 1H), 1.77 (dd, J = 1.9 & 16.0 Hz, 1H), 1.37 (m, 1H), 1.25 (m, 1H), 1.21 (m, 2H), 0.86 (m, 2H); m/z = 571 [M-lf.
Example 57 (R)-N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)-6-methoxypheny1)-1-(2,3-dihydroxypropyl)cyclopropane-1-sulfonamide:
µ--7H 0 ri NH H F
Me0 The pure R isomer was obtained by chiral HPLC separation of the racemic mixture (example 55). HN1vIR (CDC13, 300 MHz): 8 7.38 (dd, J = 1.7 & 10.3 Hz,1H), 7.26 (m, 1H), 7.14 (s, 1H), 6.87 (s, 1H), 6.53 (dd, J = 6.8 & 11.4 Hz, 1H), 6.43 (m, 1H), 4.06 (m, 1H), 3.89 (s, 3H), 3.63 (dd, J = 3.7 & 11.1 Hz, 111), 3.49 (dd, J = 6.4 & 11.1 Hz, 1H), 2.3 (dd, J = 9.7 &
16.1 Hz, 1H), 1.77 (dd, J = 1.9 & 16.0 Hz, 1H), 1.37 (m, 1H), 1.25 (m, 1H), 1.21 (m, 2H), 0.86 (m, 2H); nilz = 571 {m-if.
Example 58 1-(2-hydroxyethyl)-N-(3,4,6-trifluoro-2-(2-fluoro-4-iodophenylamino)phenyl) cyclopropane-1-sulfonamide:
Step A: TBS-protected 1-(2-hydroxyethyl)-N-(3,4,6-trifluoro-2-(2-f1uoro-4-iodophenylamino)phenyl) cyclopropane-1-sulfonamide:
OTBS
Ataqe0 According to the general procedure B, the sulfonyl chloride prepared in step C
of example 16 was reacted with 5,6-difluoro-N1-(2-fluoro-4-iodopheny1)-3-fluorobenzene-1,2-diamine to obtain the title product. Yield: 13%. 1H-NMR (300 MHz, CDC13): 6 =
7.51 (s, 1H, br), 7.37-7.35 (d, 1H), 7.27-7.25 (d, 1H), 6.94 (s, 1H, br), 6.78-6.68 (m, 1H), 6.46-6.44 (m, 111), 3.90-3.88 (t, 211), 2.12-2.10 (t, 2H), 1.31-1.28 (m, 211), 0.91-0.89 (m, 2H), 0.86 (s, 9H), 0.05 (s, 6H); m/z = 643 [M-lf.
Step B: 1-(2-hydroxyethyl)-N-(3,4,6-trifluoro-2-(2-fluoro-4-iodophenylamino)-phenyl) cyclopropane-l-sulfonamide:
(OH
Ao o' NH H F
FoN0 Same procedure as in step E, example 16. Yield: 100%. 1H-NMR (300 MHz, CDC13):
5 = 7.51 (s, 1H, br), 7.37-7.35 (d, 1H), 7.27-7.25 (d, 1H), 6.94 (s, 1H, br), 6.78-6.68 (m, 1H), 6.46-6.44 (m, 1H), 3.90-3.88 (t, 2H), 2.12-2.10 (t, 2H), 1.31-1.28 (m, 2H), 0.91-0.89 (m, 211);
nz/z = 529 [M-1T.
Example 59 N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)-6-methoxyphenyI)-1-(2-hydroxyethyl)cyclopropane-1-sulfonamide:
Step A: TBS-protected N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)-6-methoxypheny1)-1-(2-hydroxyethyl)cyclopropane-1-sulfonamide:
(OTBS
,0 NH H F
N
According to the general procedure B, the sulfonyl chloride prepared in step C
of example 16 was reacted with 5,6-difluoro-N1-(2-fluoro-4-iodopheny1)-3-methoxy-benzene-1,2-diamine to obtain the title product. Yield: 37%. 111-NM:ft (300 MHz, CDC13): 5 = 7.40-7.34 (dd, 1H), 7.23-7.21 (m, 1H), 6.61 (s, 1H, br), 6.57-6.49 (dd, 1H), 6.48-6.39 (m, 1H), 3.9-3.7 (m, 5H), 2.15-2.05 (t, 2H), 1.30-1.20 (m, 2H), 0.95-0.80 (m, 1114), 0.05 (s, 6H); m/z =
655 EM-if.
Step B: N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)-6-methoxypheny1)-1-(2-hydroxyethyl)cyclopropane-1-sulfonamide:
(OH
AlAlk, 0 lel la Same procedure as in step E, example 16. Yield: 100%. 1H-NMR (300 MHz, CDC13):
= 7.40-7.34 (dd, 1H), 7.23-7.21 (m, 1H), 6.61 (s, 1H, br), 6.57-6.49 (dd, 1H), 6.48-6.39 (m, 1H), 3.9-3.7 (m, 511), 2.15-2.05 (t, 2H), 1.30-1.20 (m, 2H), 0.95-0.80 (m, 2H); m/z = 541 [M-11".
Example 60 N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)-6-methoxypheny1)-1-(3-hydroxy-2-(hydroxymethyl)propyl)cyclopropane-l-sulfonamide:
Step A: Dimethyl 2-(2-bromoallyl)malonate:
Me0).)-LOMe Br To a suspension of sodium hydride (5.0 g, 125 mmol) in HMPA (50 ml, distilled from calcium hydride) was added a solution of dimethyl malonate (11.7 ml, 100 mmol) in HMPA
(5 ml) at 0 C under argon. The mixture was heated to 50 C and stirred 1 hour.
Following this the solution was again cooled to 0 C, and a solution of 2,3-dibromopropene (12.2 ml, 100 mmol) in HMPA (5 ml) was added to the reaction mixture. Next, the solution was warmed to 40 C and stirred for 1 hour. The reaction mixture was quenched with aq. HC1 (10%, 88 ml) and extracted with ether (3 x 45 m1). The organic fractions were collected, dried over MgS0-4, and the solvent was removed in vacuo . The crude oil was purified via silica gel chromatography (eluants: chloroform/hexane) to obtain the titled product as a colorless oil (16.3 g, 65%). H-NMR (300 MHz, CDC13) 6 5.70 (d, J = 1.8 Hz, 1 H), 5.48 (d, J
= 1.8 Hz, 1H), 3.63 (t, J = 7.5 Hz, 1 H), 3.76 (s, 6 H), 3.04 (d, J = 7.5 Hz, 2 H).
Step B: 2-(2-Bromoallyl)propane-1,3-diol:
OH OH
is Br Lithium aluminum hydride (1.9 g, 7.65 mmol) was slurried in anhydrous diethyl ether (50 ml) and cooled to -78 C in a dry ice/acetone bath. A solution of the product from step A
(0.639 g, 16.84 mmol) in dry ether (26 ml) was then added dropwise. After the malonate was added, the solution was allowed warm to room temperature and stirring was continued for 3 hours. The reaction was quenched with brine (50 ml), extracted with ethyl acetate (3 x 25 ml) and dried over MgSO4. The solvent was removed in vacuo to give the desired product (1.3 g, 86%) which was used for the next step without further purification. 1H-NMR (300 MHz, CDC13) 65.66 (d, J= 1.2 Hz, 1 H), 5.48 (d, J = 1.5 Hz, 1H), 3.86 (m, 2 H), 3.73 (m, 2 H), 2.51 (d, J = 7.5 Hz, 2 H), 2.40 (br s, 2 H), 2.15 (m, 1 H).
Step C: Di-tert-butyldimethylsilyl protected 2-(2-bromoallyl)propane-1,3-diol:
TBSO¨\ )¨Br TBSO--/
The product from step B (2.8 g, 14.20 mmol) was dissolved in anhydrous THF
(140 m1). Anhydrous pyridine (2.5 ml, 31.24 mmol) was added, and the solution was cooled to 0 C. tert-Butyldimethylsilyltriflate (7.2 ml, 31.24 mmol) was added dropwise, and upon completion, the reaction solution was heated to 35 C. After stirring for 6 days, the reaction was quenched with 100 ml brine, extracted with ethyl acetate (3 x 50 ml) and dried over MgSO4. The combined organic phases were evaporated to obtain the crude product (5.5 g, 91%) as a yellow oil which was used in the next step without further purification. 1H-NMR
(300 MHz, CDC13) 8 5.54 (d, J = 0.9 Hz, 1 H), 5.40 (d, J = 1.2 Hz, 1H), 3.55 (d, J = 5.4, 4 H), 2.40 (d, J = 6.9 Hz, 2 H), 1.97 (m, 1 H), 0.85 (s, 18 H), 0.02 (s, 911).
Step D: Di-tert-butyldimethylsilyl protected 24(1-bromocyclopropyl)methyl) propane-1,3-diol:
TBSO-\
A reaction flask was charged with anhydrous CH2C12 (10 ml) and diethyl zinc (1.0 M
in hexanes, 4.65 ml, 4.65 mmol) at 0 C. Trifluoroacetic acid (0.358 ml, 4.65 mmol) was added dropwise and the solution was allowed to stir for 20 minutes.
Diiodomethane (0.375 ml, 4.65 mmol) was then added and the solution was stirred for another 20 minutes. Finally, the product from step C (0.492 g, 1.16 mmol) was added and the solution was allowed to warm to ambient temperature, stirring for 16 hours. The reaction was quenched with saturated aqueous NH4C1. The layers were partitioned and the aqueous phase was extracted with chloroform (3 x 5 m1). The combined organic phases were washed with brine (10 ml), dried over MgSO4, and the volatiles were removed in vacuo. The resulting crude was purified via silica gel chromatography (eluants: chloroform/hexanes) to provide the product as a clear oil (0.280 g, 64%). 1H-NMR (300 MHz, CDC13) 6 3.66 (d, J = 5.4, 4 H), 2.08 (m, 1 H), 1.64 (d, J = 6.9, 211), 1.13 (m, 2 H), 0.88 (s, 18 H), 0.81 (m, 2 H), 0.04 (s, 911).
Step E: Di-tert-butyldimethylsilyl protected 1-(3-hydroxy-2-(hydroxymethyl)propyl) cyclopropane-l-sulfonyl chloride:
TBSO--\
it __________________________________________ 0 The product from step D (0.507 g, 1.16 mmol) was dissolved in anhydrous ether (6 ml) and the reaction solution was cooled to -78 C. Following this, tert-butyllithium (1.7 M in pentane, 1.50 ml, 2.55 mmol) was added dropwise over 5 minutes. After stirring for 0.5 hours, the lithiated product was transferred via cannula to a stirred solution of sulfuryl chloride (0.206 ml, 2.55 mmol) in dry ether (6 ml) at -78 C. Once the transfer is complete, the solution was allowed to warm to room temperature, the solvent was evaporated and the resulting white solid was slurried in dry hexanes. This slurry was immediately filtered through celite, and all volatiles were removed in vacuo. The resulting crude product (0.376 g, 71%) was isolated as a yellow oil and was used in the following step without further purification. 1H-NMR (300 MHz, CDC13) 8 3.60 (m, 4 H), 2.16 (m, 1 H), 2.03 (d, 2 H), 0.88 (s, 18 H), 0.04 (s, 9 H).
Step F: Di-tert-butyldimethylsilylprotected N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)-6-methoxypheny1)-1-(3-hydroxy-2-(hydroxymethyl)propyl) cyclopropane-1-sulfonamide:
TBS\O 0,TBS
4Y,0 01 'NH
N
5,6-difluoro-N1-(2-fluoro-4-iodopheny1)-3-methoxybenzene-1,2-diamine (8.8 mg, 0.022 mmol) was dissolved in anhydrous pyridine (0.5 ml) under an argon atmosphere. The product from step E (20.5 mg, 0.045 mmol), dissolved in dry pyridine (0.5 ml), was added to the reaction flask and the mixture was heated at 80 C for 21 hours. The solvent was removed in vacuo and the resulting crude was purified via silica gel chromatography (eluents: ethyl acetate/hexanes) to provide the title compound (2.75 mg, 15%). m/z 813.5 (M-1).
Step G: N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)-6-methoxypheny1)-1-(3-hydroxy-2-(hydroxymethyl)propyl)cyclopropane-1-sulfonamide:
OH OH
,K
0/ 'NH F
H
F I
F
The product from step F (27.9 mg, 0.0342 mmol) was dissolved in THF (1 ml) and treated with aqueous HC1 (1.2 N, 0.2 ml) at 0 C. The resulting solution was stirred for 4 hours. Following this, the reaction was quenched with saturated aqueous NaHCO3, extracted with ethyl acetate, dried over MgSO4 and the volatiles were removed in vacuo.
The resulting crude was purified via silica gel chromatography (eluents:
methanol/chloroform) followed by LC-MS purification to provide the title compound (11.8 mg, 59%). 11-1-NMR (300 MHz, CD30D) 8 7.32 (dd, 1 H), 7.21 (d, 1 H), 6.76 (dd, 1 H), 6.33 (m, 1 H), 3.82 (s, 3 H), 3.52 (d, 4 H), 2.01 (m, 1 H), 1.88 (d, 2 H), 1.07 (m, 2 H), 0.75 (m, 2 H), m/z 585.3 (M-1).
Example 61 N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)-6-methoxyphenyl) cyclobutane sulfonamide:
Step A: Cyclobutanesulfonyl chloride:
q so,ci To a suspension of Mg turnings (0.790 g, 32.5 mmol) in 20 ml anhydrous diethyl ether was added a solution of cyclobutylbromide (1.8 ml, 2.5722 g, 19.1 mmol) in 20 ml diethyl ether in small portions with strong stirring. After the initial exothermic reaction had ceased, the mixture was further heated to the reflux temperature for 30 min.
The suspension was cooled down to room temperature and the supernatant was added in small portions to an ice-cold solution of sulfuryl chloride (4.6 ml, 7.728 g, 57.2 mmol) in 30 ml anhydrous DCM.
After complete addition, the suspension was warmed to room temperature and the volatiles were removed in vacuo. The residue was dried in oil-pump vacuo for 15 min, then it was extracted with hexane (150 m1). The hexane suspension was filtered and the hexane was removed in vacuo to give the crude product as dark purple oil which was used for the next step without further purification. There is still some unreacted cyclopropylbromide present.
Crude yield: 1.1 g (38%).
Step B: N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)-6-methoxyphenyl) cyclobutanesulfonamide Me0 N
According to the general procedure B, the cyclobutylsulfonyl chloride prepared in the step above was reacted with 5,6-difluoro-N1-(2-fluoro-4-iodopheny1)-3-methoxy-benzene-1,2-diamine to obtain the title product. Yield: 75%. 1H-NMR (300 MHz, CDC13):
8 = 7.44 (s, 1H, br), 7.41-7.36 (dd, 1H), 7.24-7.23 (m, 1H), 6.54-6.38 (m, 2H), 5.90 (s, 1H, br), 3.85-3.75 (m, 5H), 2.60-2.40 (m, 2H), 2.25-2.15 (m, 1H), 2.15-1.95 (m, 2H); m/z = 511 [MAI.
Example 62 N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)-6-methylpheny1)-1-(2,3-dihydroxypropyl)cyclopropane-l-sulfonamide:
Step A: (3,4,5-Trifluorophenyl)methanol:
HO
To a cooled (-5 C) solution of 3,4,5-trifluorobenzaldehyde (7.0 g, 43.75 mmol) in a mixture ( 50 ml, 9:1) of THF and water NaBH4 (1.662 g, 43.75 mmol) was slowly added in portions over a period of 30 min. The reaction mixture was allowed to attain room temperature over a period of 2h and carefully poured into ice-cold dil HC1 (200 ml, 1N). The oily layer was extracted into CH2C12 (250 ml) and the organic layer washed with water (200 ml), dried (MgSO4) and evaporated. The crude product (7.08 g, quantitative) obtained was taken forward without further purification.
Step B: 5-(Bromomethyl)-1,2,3-trifluorobenzene:
Br F
To a solution of the (3,4,5-Trifluorophenyl)methanol (40 mmol) in CH2C12 (150 ml), a solution of thionyl bromide (6.16 ml, 80 mmol) in CH2C12 (50 ml) was added slowly. The reaction mixture stirred at room temperature for 16h and poured into ice-water (200 ml). The organic layer was separated and washed with saturated NaHCO3 (2x200 ml), water (200 ml), dried (MgSO4) and evaporated to obtain the corresponding bromo compound as a pale yellow oil in quantitative yield. The crude product was carried forward for the next reaction without further purification.
Step C: 1,2,3-Trifluoro-5-methylbenzene:
The above bromo compound (40 mmol) was mixed with triethylsilane (48 mmol) and the reaction mixture was treated with solid PdC12 (4 mmol) in small portions.
After a few minutes a vigorous exothermic reaction was ensued and care was taken to reflux the contents of the flask by placing a reflux condenser. The reaction mixture was stirred at room temperature for additional 6h and the contents were allowed to settle over 16h. Then the crude liquid product was decanted carefully and carried forward for the next reaction without further purification. It was assumed tat the reaction proceeds in quantitative yield.
Step D: 1,2,3-Trifluoro-5-methy1-4-nitrobenzene:
HC ,F
1,2,3-Trifluoro-5-methylbenzene (40 mmol) was added to conc. H2SO4 (50 ml) at C. Then the reaction mixture was slowly treated with conc. HNO3 (3.39 ml, 48.44 mmol, 90%) while maintaining the internal temperature below 20 C. The reaction mixture was stirred at room temperature for 16h and poured onto ice (300 g) and the oily layer was extracted with CH2C12 (2x125 ml). The organic layer was washed with water (2x200 ml), brine (200 ml) and dried (MgSO4) and evaporated to obtain the crude product which was purified over flash silica gel chromatography to obtain the title product (6.5 g, 85%). 1H
NMR (300 MHz, CDC13): 8 6.96 (septet, 1H), 2.39 (s, 3H). 19F NMR (CDC13): 8 -128.18, -141.50, -159.05.
Step E: 2,3-Difluoro-N-(2-fluoro-4-iodopheny1)-5-methyl-6-nitroani1ine:
2-Fluoro-4-iodoaniline and 1,2,3-trifluoro-5-methy1-4-nitrobenzene were reacted using the condition described in Example 1 (Step A) to form the title compound. M-H+:
407.9 Step F: 5,6-Difluoro-N1-(2-fluoro-4-iodopheny1)-3-methylbenzene-1,2-diamine:
2,3-Difluoro-N-(2-fluoro-4-iodopheny1)-5-methy1-6-nitroaniline was reduced using the condition described in Example 1 (step B) to form the title compound. M-114.: 377.4 Step G: 1-Allyl-N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)-6-methylphenyl)cyclopropane-l-sulfonamide:
61:
According to the general procedure B, 1-allyl-cyclopropanesulfonyl chloride (142 mg, 142 mg) was reacted with 5,6-difluoro-N1-(2-fluoro-4-iodopheny1)-3-methylbenzene-1,2-diamine (150 mg, 0.4 mmole) to obtain the title product (100 mg, 47%); m/z =
521 [M-lf.
Step H: N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)-6-methylpheny1)-1-(2,3-dihydroxypropyl)cyclopropane-1-sulfonamide:
r...7H
HO ,p 0'19 NH H F
1-Allyl-N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)-6-methylphenyl) cyclopropane-l-sulfonamide ( 150 mg, 0.29 mmole) and 4-methylmorpholine N-oxide (33 mg, 0.29 mmole) was dissolved in THF (5 mL). Osmium tetroxide was added at room temperature (0.029 mmole, 0.18 mL, 4% in H20) and the reaction mixture was stirred at room temperature for 16 hours. Et0Ac was added, the organic phase was washed with water, dried (MgSO4) and concentrated under reduced pressure. The residue was purified over silica gel chromatography (eluants: Et0Ac/ Me0H) to obtain the titled product (0. 110 g, 68 %). 1H
NMR (300 MHz, CDC13): 8 7.07 (m, 1H), 6.97 (br m, 2H), 6.84 (m, 21-1), 6.60 (br m, 2H), 3.98 (br m, 1H), 3.58 (m, 1H), 3.43 (m, 1H), 3.20 (d, J= 3.9 Hz, 1H), 2.42 (s, 3H), 2.31 (dd, J= 9.9 & 15.6 Hz, 1H),2.01 (br t, 1H),2.31 (dd, J= 9.9 & 15.6 Hz, 1H), 1.66 (dd, J= 2.1 &
15.9 Hz, 1H), 1.52 (m, 1H), 1.40 (m, 1H), 0.91 (m, 2H).
Example 63 1-(2,3-Dihydroxypropy1)-N-(6-ethyl-3,4-difluoro-2-(2-tluoro-4-iodophenylamino) phenyl) cyclopropane-l-sulfonamide:
Step A: 1-(3,4,5-Trifluorophenypethanol:
An ethereal solution (17.41 ml, 52.24 mmol, 3M) of MeMgBr was slowly added at -78 C to a solution of 3,4,5-trifluorobenzaldehyde (6.96 g, 43.53 mmol) in THF
(125 m1). The reaction mixture was stirred at room temperature for 16h and was cooled (0 C) and was quenched, sequentially, with excess ethyl acetate (10 ml) and water (5 m1).
Excess anhydrous MgSO4 (5 g) was added and stirred for 30 minutes at room temperature. The suspension was filtered over celite and the solids were washed with ethyl acetate (2x25 m1).
The combined filtrate was evaporated to obtain the product in quantitative yield (7.65 g).
Step B: 5-(1-Bromoethy0-1,2,3-trifluorobenzene:
Br To a solution of the 1-(3,4,5-Trifluorophenyl)ethanol: (7.65 g, 43.5 mmol) in (250 ml), a solution of thionyl bromide (18.1 g, 87 mmol) in CH2C12 (50 ml) was added slowly. The reaction mixture stirred at room temperature for 16b and poured into ice-water (200 m1). The organic layer was separated and washed with saturated NaHCO3 (2x200 ml), water (200 ml), dried (MgSO4) and evaporated to obtain the corresponding bromo compound as a pale yellow oil in quantitative yield (10.4 g). The crude product was carried forward for the next reaction without further purification.
Step C: 5-Ethyl-1,2,3-trifluorobenzene:
F
The above bromo compound (9.65 g, 40.4 mmol) was mixed with triethylsilane (41 mmol) and the reaction mixture was treated with solid PdC12 (177 mg, 4 mmol) in small portions. After a few minutes a vigorous exothermic reaction was ensued and care was taken to reflux the contents of the flask by placing a reflux condenser. The reaction mixture was stirred at room temperature for additional 6h and the contents were allowed to settle over 16h.
Then the crude liquid product was decanted carefully and carried forward for the next reaction without further purification. It was assumed tat the reaction proceeds in quantitative yield.
Step D: 1 -Ethyl-3,4,5-trifluoro-2-nitrobenzene:
F
1,2,3-Trifluoro-5-methylbenzene (6.46 g, 40.4 mmol) was added to conc. H2SO4 (50 ml) at 0-5 C. Then the reaction mixture was slowly treated with conc. HNO3 (3.39 ml, 48.44 mmol, 90%) while maintaining the internal temperature below 20 C. The reaction mixture was stirred at room temperature for 16h and poured onto ice (300 g) and the oily layer was extracted with CH2C12 (2x125 ml). The organic layer was washed with water (2x200 ml), brine (200 ml) and dried (MgSO4) and evaporated to obtain the crude product which was purified over flash silica gel chromatography to obtain the title product (6.6 g, 79%). 111 NMR (CDC13): 6.98 (septet, 1H), 2.68 (q, 211), 1.26 (t, 7.8 & 7.2 Hz, 311).
Step E: 3-Ethyl-5,6-difluoro-N-(2-fluoro-4-iodopheny1)-2 nitroaniline:
2-Fluoro-4-iodoaniline (2.05 g, 10 mmole) and 1-ethy1-3,4,5-trifluoro-2-nitrobenzene (2.37 g, 10 mmole) were reacted using the condition described in example 1 (Step A) to form the title compound (2.47 g, 60%); nilz = 407 [M-1)".
Step F: 3-Ethyl-5,6-difluoro-N1-(2-fluoro-4-iodophenyl)benzene-1,2-diamine:
N
1,2,3-Trifluoro-5-methy1-4-nitrobenzene (2.47 g, 5.85 mmole) was reduced using the condition described in example 1 (Step B) to form the title compound. M-H+:
Step G: 1-Allyl-N-(6-ethy1-3,4-difluoro-2-(2-fluoro-4-iodophenylamino)phenyl)cyclopropane-l-sulfonamide:
r According to the general procedure B, 1-allyl-cyclopropanesulfonyl chloride (230 mg, 1.27 mmole) was reacted with 5,6-difluoro-N1-(2-fluoro-4-iodopheny1)-3-methylbenzene-1,2-diamine (100 mg, 0.255 mmole) to obtain the title product (72 mg, 53%);
771/Z = 535 [M-11".
Step H: 1-(2,3-Dihydroxypropy1)-N-(6-ethy1-3,4-difluoro-2-(2-fluoro-4-iodophenylamino)phenyl)cyclopropane-l-sulfonamide:
01 v....7H
HO ,p d'S 'NH H F
1-Allyl-N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)-6-methylphenyl) cyclopropane-1 -sulfonamide ( 70 mg, 0.13 mmole) and 4-methylmorpholine N-oxide (15 mg, 0.13 mmole) was dissolved in THF (2 mL). Osmium tetroxide was added at room temperature (0.013 mmole, 0.075 mL, 4% in H20) and the reaction mixture was stirred at room temperature for 16 hours. Et0Ac was added, the organic phase was washed with water, dried (MgSO4) and concentrated under reduced pressure. The residue was purified over silica gel chromatography (eluants: Et0Ac/ Me0H) to obtain the titled product. 1H NMR
(300 MHz, CDC13): 8 7.38 (dd, J= 2.1 & 10.8 Hz, 1H), 7.27 (m, 2H), 7.12 (br s, 1H), 6.91 (dd, J=
8.1 & 10.8 Hz, 1H), 6.69 (br s, 1H), 6.36 (dt, J= 4.8, 8.7 & 13.5 Hz, 1H), 4.00 (m, 1H), 3.62 (dd, J= 3.6 & 10.5 Hz, 1H), 3.47 (br m, 2H), 2.81 (q, 2H), 2.40 (dd, J= 10.2 &
15.9 Hz, 1H), 1.73 (br m, 2H), 1.58 (in, 1H), 1.43 (m, 111), 0.94 (m, 2H).
Example 64 N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)-6-(2-methoxyethoxy)pheny1)-1-(2,3-dihydroxypropyl)cyclopropane-1-sulfonamide:
Step A: 1,2,3-Trifluoro-5-(2-methoxyethoxy)-4-nitrobenzene:
To a mixture of 3,4,5-trifluoro-2-nitrophenol (1.93, 10 mmol), Ph3P (3.93 g, mmol), and 2-methoxy-ethanol (1.18 ml, 15 mmol) in anhydrous THF (25 ml) a solution of diisopropyl azodicarboxylate (2.91 ml, 15 mmol) in THF (5 ml) was added at 0 C and the reaction mixture was stirred at room temperature for 16h. The volatiles were evaporated and the residue was dissolved in CH2C12 (100 ml) and the organic layer was washed with water (100 ml), brine (100 ml) dried (MgSO4) and evaporated. The residue obtained was purified over flash silica gel chromatography to obtain the titled product in 68% (1.70 g) yield. 1H
NMR (300 MHz, CDC13): 8 6.78 (ddd, J= 2.4, 6.0, 11.7 Hz, 1H), 4.19 (t, J= 4.5 Hz, 2H), 3.72 (t, J= 4.5 Hz, 214), 3.39 (s, 3H).
Step B: 2,3-Difluoro-N-(2-fluoro-4-iodopheny1)-5-(2-methoxyethoxy)-6-nitroaniline:
2-Fluoro-4-iodoaniline (1.6 g, 6.8 mmole) and 1,2,3-trifluoro-5-(2-methoxyethoxy)-4-nitrobenzene (1.7 g, 6.8 mmole) were reacted using the condition described in Example 1 (Step A) to form the title compound (1.02 g, 32 %); m/z = 467 [M-11".
Step C: 5,6-Difluoro-N1-(2-fluoro-4-iodopheny1)-3-(2-methoxyethoxy)benzene-1,2-diamine:
-... ..--,, 0 0 N lei F I
F
2,3-Difluoro-N-(2-fluoro-4-iodopheny1)-5-(2-methoxyethoxy)-6-nitroaniline (1.017 g, 2.17 mmole) was reduced using the condition described in Example 1 (Step B) to form the title compound; m/z = 337 [M-1]-.
Step D: 1-Allyl-N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)-6-(2-methoxyethoxy)phenyl)cyclopropane-1-sulfonamide:
4rf Irjr, 13'-- 'NH F
H
OC) 0 F I
F
According to the general procedure B, 1-allyl-cyclopropanesulfonyl chloride (450 mg, 2.5 mmole) was reacted with 5,6-difluoro-N1-(2-fluoro-4-iodopheny1)-3-(2-methoxyethoxy)benzene-1,2-diamine (219 mg, 2.5 mmole) to obtain the title product (230 mg, 78%); m/z = 581 [M-lf..
Step E: N-(3 ,4-d ifluoro-2-(2-fluoro-4-iodophenylamino)-6-(2-methoxyethoxy)pheny1)-1-(2,3-dihydroxypropyl)cyclopropane-1-sulfonamide:
HOjJ,?
O''S NH H F
1-allyl-N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)-6-(2-methoxyethoxy) phenyl) cyclopropane-1-sulfonamide ( 230 mg, 0.395 mmole) and 4-methylmorpholine N-oxide (46 mg, 0.395 mmole) was dissolved in THF (2 mL). Osmium tetroxide was added at room temperature (0.039 mmole, 0.25 mL, 4% in H20) and the reaction mixture was stirred at room temperature for 16 hours. Et0Ac was added, the organic phase was washed with water, dried (MgSO4) and concentrated under reduced pressure. The residue was purified over silica gel chromatography (eluants: Et0Ac/ Me0H) to obtain the titled product. III
NMR (300 MHz, CDC13): 67.36 (dd, J= 1.8 & 10.5 Hz, 1H), 7.27 (m, 2H), 6.56 (dd, J= 6.9 & 11.4 Hz, 111), 6.40 (dt, J----- 5.7,7.5 & 12.9 Hz, 1H), 4.17 (m, 2H), 4.01 (m, 1H), 3.78 (m, 2H), 3.60 (dd, J= 3.6 & 11.1 Hz, 1H), 3.47 (m, 1H), 3.45 (s, 3H), 2.36 (dd, J= 9.6 &
15.9 Hz, 1H), 1.78 (dd, J= 2.4 & 15.6 Hz, 1H), 1.45-1.25 (m, 2H), 0.89 (m, 2H).
Example 65 2,4-diehloro-N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)phenyl) benzene sulfonamide:
CI lei CI
Is' NH
Synthesized by method A using the appropriate sulfonyl chloride. m/z --= 571 [M-1I.
Example 66 2-chloro-N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)pheny1)-4-(trifluoromethyl) benzenesulfonamide:
o Synthesized by method A using the appropriate sulfonyl chloride. inlz 605 [M-11`.
Example 67 N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)pheny1)-2-(trifluoromethoxy) benzene sulfonamide:
yF3 oo "NH H F
N
Synthesized by method A using the appropriate sulfonyl chloride. mth = 587 [M-1I.
Example 68 4-(N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)phenyl)sulfamoyl)benzoic acid:
HOOC
Si N
Synthesized by method A using the appropriate sulfonyl chloride. nilz = 584 [1\4-1f.
Example 69 N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)phenyl)benzenesulfonamide:
s, F
F I
F
Synthesized by method A using the appropriate sulfonyl chloride. m/z = 503 [M-lf.
Example 70 N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)phenyI)-2-fluorobenzene sulfonamide:
s, F
F I
F
Synthesized by method A using the appropriate sulfonyl chloride. m/z = 521 [M-11".
General procedure D: substitution of the iodine atom:
A suspension containing 1 eqv. aryl iodide, 1.5 equiv. of the boronic acid or boronic ester, 0.25 eqv. PdC12(dppf) x DCM and10 eqv. anhydrous K2CO3 powder in a deoxygenated mixture of dioxane and water (3:1) was heated in a microwave reactor for 60 min at 115 C.
It was extracted using aq. NH4C1/ THF, and the organic fraction was dried using Na2SO4.
The crude reaction products were purified using flash-column chromatography (Si, EtAc /
Hexanes, or CHCI3 / Me0H). Yields: 20-40%.
Example 71 N-(3,4-dffluoro-2-(2-fluoro-4-methylphenylamino)phenyl)cyclopropanesulfonamide;
,A, P
s, cr NH H F
F
General procedure D :1H-NMR (500 MHz, CDCI3): 8 = 7.38-7.36 (m, 1H), 7.06-7.03 (q, 1H), 6.92-6.90 (1H), 6.73-6.72 (d, 1H), 6.63 (s, 1H, br), 6.37-6.33 (t, 1H), 5.54 (s, 1H, br), 2.42-2.39 (m, 1H), 2.25 (s, 3H), 1.14-1.11 (m, 2H), 0.94-0.90 (m, 2H); mlz =
355 [M-ir.
Where racemic mixtures of chiral compounds have been resolved into separate enantiomers, the phrase "substantially free" of the epimer, as used herein, means an enantiomeric excess of at least 90%.
=
Biolvical activity Generation of ICSO Data Materials and preparation of reagents: Human GST-MEK1 and the constitutively active allele GST-MEK1cA (harboring the mutations Ser218Asp and Ser222Asp) were subcloned into the yeast expression vector pGEM4Z (Promega, Madison, WI) from the wild type human MEKI cDNA. GST-MEK1cA was expressed in Escherichia coil and partially purified using Glutathione Sepharose 4B affinity resin (Amersham Pharmacia Biotech, Piscataway, NJ). The ERK2 allele was subcloned from MAPK2/Erk2 cDNA (wild type) in pUSEamp (Upstate Biotechnology, Inc., Waltham, MA) into the vector pET2la (Novagen, Madison, WI) resulting in an N-terminal histidine-tagged mouse ERK2 allele.
ERK2 was expressed and purified to homogeneity. Myelin basic protein (MB?) was purchased from Gibco BRL (Rockville, MD). EasyTides adenosine 5'-triphosphate (ATP) (jy-33P}) (NEN Perkin Elmer, Wellesley, MA) was the source of radiolabel for all lcinase reactions. Activated Raf-1 (truncated) and activated MAPKinase 2/ERK2 were purchased TM
from Upstate, Inc. (Lake Placid, NY), 4-20% Criterion Precast gels were purchased from 1310-Rad (Hercules, CA).
Determination of enzymatic activity: Compounds were diluted from dimethylsulfoxide (DMSO) stocks into IxHMNDE (20 mM HEPES pH 7.2, 1 mM MgC12, 100 mM NaC1, 1.25 mM DTT, 0.2 mM EDTA). A typical 25-microliter assay contained 0.002 nanomoles MEK1cA, 0.02 nanomoles ERK2, 0.25 nanomoles MB?, 0.25 nanomoles unlabeled ATP, and 0.1 Ci Ey33133 ATP. The screening assay essentially comprised four additions. Five I of diluted compound were dispensed to 96-well assay plates.
Ten 1 of 2,5x enzyme cocktail (MEK1CA and ERK2 only) were then added to each well followed by a pre-incubation for 30 minutes at ambient temperature. Ten I of 2.5x substrate cocktail (labeled and unlabeled ATP plus MB?) were then added, followed by incubation for 60 minutes at ambient temperature. Finally, 100 id of 10% trichloroacetic acid (TCA) were added and incubated for 30 minutes at room temperature to halt the reaction and precipitate radiolabeled protein products. Reaction products were harvested on glass fiber 96 well filter plates prewetted with water and 1% pyrophosphate. The filter plate was then washed 5 times with water. Water was displaced by absolute ethanol and the plate was allowed to air dry for 30 minutes at room temperature. A back seal was applied manually and 40 pl of scintillation =
cocktail were dispensed to each well. A top seal was applied and the plate was counted in the TopCount for two seconds per well.
For certain experiments a truncated version of MEK that requires activation by Raf kinase were used.
Generation of EC5O Data Effects of compounds in the cell were determined by Western blotting for phosphorylated ERIC. MDA-MB-231 breast cancer cells were plated in a 48 well plate at 20,000 cells per well and grown in a 37 humidified CO2 incubator. The following day, the growth media (DMEM + 10% fetal bovine serum) was removed and replaced with starve media (DMEM + 0.1% fetal bovine serum). Cells were incubated in the starve media for sixteen hours and then treated with a range of compound concentrations for thirty minutes.
After incubation with compound, cells were stimulated with 10Onghnl EGF for five minutes.
The cells were then lysed and analyzed by Western blot using a monoclonal antibody raised to phosphorylated ERIC. The signal was amplified using a secondary antibody conjugated to a near -IR. dye and detected on a Licor OdysseyTm scanner. The intensity of signal was quantitated and this data was used to generate dose response curves and EC50 calculations.
Legend: A, EC50= < 2.0nM; B, EC50= 2.0-15nM; C, EC50 = 15nM-100nM;
D, EC50> 100nM, IC50 < 20 M; F, EC50> 100nM, 1050> 20 M
Compound Structure ACTIVITY pM
Number ei NH 001 1001 o N A
NH
Compound Structure ACTIVITY IJM
Number _ 1 i =''S
/'/ N
NH
SF' I
F
.--------,e C
NH
F I
F
s //N
F 0 NH so F I
F
(--i, S 6, 0 NH so F I
F
0 g F I
F
cl,õ0 s F I
F _ al F I
F
Compound Structure ACTIVITY pM
Number >(s/Y
NH =
I/
ON
--S
s NH
ak /5) o NH
NH
NH
el la eo NH
Compound Structure ACTIVITY pM
Number NH
NH
NH
NH
HO
(Racemic) A
If N
OH
1019 ,9 (Racemic) A
// N
NH
Compound Structure ACTIVITY 01 Number HO
(Racemic) 0 A
II
\NH
Ho F NH
OH
(R isomer) A
NH
pH
HO
(S isomer) szy // N
HO
HO,õ.
(R isomer) NH
F NH Is Compound Structure ACTIVITY pM
Number HO
2i)) (S isomer) NH
F NH
1025 n NH
Ao¨
NH
= 40 OH
s_+ A
--o¨
o¨
NH
si NH 401 OH OH
A
NH
Compound Structure ACTIVITY pM
Number \
NH
NH
1030 \
NH
SFSI
OH
\ A
NH
31 (a-e) 2-F-3 -C I-phenyl Cl Compound A = Rid, An, or Ar2 X
#
32 (a-e) 2-F-3-C1-phenyl F
33 (a-e) 2-F-4-CI-phenyl CI
34 (a-e) 2-F-4-CI-phenyl F
35 (a-e) 2-F-5-Cl-phenyl Cl 36 (a-e) 2-F-5-C1-phenyl F
37 (a-e) 3-cyano-4-F-phenyl Cl 38 (a-e) 3-cyano- 4-F-phenyl F
39 (a-e) 2-Cl-phenyl Cl 40 (a-e) 2-Cl-phenyl F
41 (a-e) 3-Cl-phenyl Cl , 42 (a-e) 3-Cl-phenyl F
43 (a-e) 4-Cl-phenyl Cl 44 (a-e) 4-Cl-phenyl F
45 (a-e) 2,3-di-Cl-phenyl Cl 46 (a-e) 2,3-di-Cl-phenyl F
47 (a-e) 2,5-di-Cl-phenyl Cl 48 (a-e) 2,5-di-Cl-phenyl F
49 (a-e) 2,6-di-Cl-phenyl Cl 50 (a-e) 2,6-di-Cl-phenyl F
51 (a-e) 3,5-di-Cl-phenyl Cl 52 (a-e) 3,5-di-Cl-phenyl F
53 (a-e) 2,4-di-Cl-phenyl Cl 54 (a-e) 2,4-di-Cl-phenyl F
55 (a-e) 3,4-di-Cl-phenyl Cl 56 (a-e) 3,4-di-Cl-phenyl F
57 (a-e) 2,4,6-tri-Cl-phenyl Cl 58 (a-e) 2,4,6-tri-Cl-phenyl F
59 (a-e) 2-C1-4-CF3-phenyl Cl 60 (a-e) 2-C1-4-CF3-phenyl F
61 (a-e) 2-CF3-phenyl Cl 62 (a-e) 2-CF3-phenyl F
63 (a-e) 3-CF3-phenyl Cl 64 (a-e) 3-CF3-phenyl F
65 (a-e) 4-CF3-phenyl Cl 66 (a-e) 4-CF3-phenyl F
67 (a-e) 2-CF30 phenyl Cl 68 (a-e) 2-CF30 phenyl F
69 (a-e) 3-CF30 phenyl Cl 70 (a-e) 3-CF30 phenyl F
71 (a-e) 4-CF30 phenyl Cl 72 (a-e) 4-CF30 phenyl F
73 (a-e) 4-CliF20-phenyl Cl 74 (a-e) 4-CHF20-phenyl F
75 (a-e) 2-methyl-5-nitro-phenyl Cl 76 (a-e) 2-methyl-5-nitro-phenyl F
77 (a-e) 2-cyano-phenyl Cl Compound A = Rid, Ari, or Ar2 X
78 (a-e) 2-cyano-phenyl 79 (a-e) 3 -cyano-phenyl Cl 80 (a-e) 3 -cyano-phenyl 81 (a-e) 4-cyano-phenyl Cl 82 (a-e) 4-cyano-phenyl 83 (a-e) 4-methoxy-phenyl Cl 84 (a-e) 4-methoxy-phenyl 85 (a-e) 3,4-dimethoxy-phenyl Cl 86 (a-e) 3,4-dimethoxy-phenyl 87 (a-e) 3-carbamyl-phenyl Cl 88 (a-e) 3-carbamyl-phenyl 89 (a-e) 3-carboxyl-phenyl Cl 90 (a-e) 3-carboxyl- phenyl 91 (a-e) 3-(N,N-dimethylcarbamoyl)phenyl Cl 92 (a-e) 3-(N,N-dimethylcarbamoyl)phenyl F
93 (a-e) 4-methylsulfonyl-phenyl Cl 94 (a-e) 4-methylsulfonyl-phenyl 95 (a-e) 3-(1,3,4 oxadiazol-2-yl)phenyl Cl 96 (a-e) 3-(1,3,4 oxadiazol-2-yl)phenyl 97 (a-e) 3-(1,3,4 thiadiazol-2-yl)phenyl Cl 98 (a-e) 3-(1,3,4 thiadiazol-2-yl)phenyl 99 (a-e) 3 -(5-methyl-1,3,4-oxadiazol)phenyl Cl 100 (a-e) 3-(5-methyl-1,3,4-oxadiazoOphenyl F
101 (a-e) 3-(5-methyl-1,3,4-thiadiazoOphenyl Cl 102 (a-e) 3-(5-methyl-1,3,4-thiadiazol)phenyl F
103 (a-e) 3 -am id inyl-phenyl Cl 104 (a-e) 3-am id inyl-phenyl 105 (a-e) 3 -(1H-tetrazolyl)phenyl Cl 106 (a-e) 3-(1H-tetrazolyl)phenyl 107 (a-e) 4-acetamido-phenyl Cl 108 (a-e) 4-acetamido-phenyl 109 (a-e) 3-C1-4-[(N-morpholinylcarbonyl) Cl amino]phenyl 110 (a-e) 3-C1-4-[(N-morpholinylcarbonyl) amino]phenyl 111 (a-e) 3-C1-4-[(N-pyrrolidinylcarbonyl) Cl amino]phenyl 112 (a-e) 3-C1-4- [(N-pyrro I idinylcarbonyl) amino]phenyl 113 (a-e) 3,5-dimethylisoxazoly1 Cl 114 (a-e) 3,5-dimethylisoxazoly1 115 (a-e) 4-(N-morpholinylsulfonyl)phenyl Cl 116 (a-e) 4-(N-morpholinylsulfonyl)phenyl 117 (a-e) 3-F-benzyl Cl 118 (a-e) 3-F-benzyl 119 (a-e) 4-F-benzyl Cl Compound A = Rub Ari, or Ar2 X
120 (a-e) 4-F-benzyl 121 (a-e) 3-F-phenyl-ethyl Cl .122 (a-e) 3-F-phenyl-ethyl 123 (a-e) 4-F-phenyl-ethyl Cl 124 (a-e) 4-F-phenyl-ethyl 125 (a-e) 8-quinolinyl Cl 126 (a-c) 8-quinolinyl 127 (a-e) 2-thienyl CI
128 (a-c) 2-thienyl 129 (a-e) 2,3-di-C1-thien-5-y1 Cl 130 (a-e) 2,3-di-C1-thien-5-y1 131 (a-e) 1,3,5 trimethy1-1H-pyrazoly1 Cl 132 (a-e) 1,3,5 trimethy1-1H-pyrazoly1 133 (a-e) 1,3-dimethy1-5-C1-1H-pyrazoly1 Cl 134 (a-e) 1,3-dimethy1-5-C1-1H-pyrazoly1 135 (a-e) 1-methy1-3-CF3-1H-pyrazol-4-y1 Cl 136 (a-c) 1-methy1-3-CF3-1H-pyrazol-4-y1 137 (a-e) 2-acetamido-4-methyl-thiazol-5-y1 Cl 138 (a-c) 2-acetamido-4-methyl-thiazol-5-y1 F
139 (a-c) 2,4-dimethyl-thiazol-5-y1 CI
140 (a-e) 2,4-dimethyl-thiazol-5-y1 141 (a-e) 1,2-dimethy1-1H-imidazol-4-y1 Cl 142 (a-c) 1,2-dimethy1-1H-imidazol-4-y1 Synthetic Procedures and Examples Compounds of this invention can be prepared by a variety of methods. The procedures below are intended to illustrate those methods, and the examples given are intended to illustrate the scope of this invention. Neither the methods not the examples should be construed as limiting the invention in any way.
I. The preparation of compound of formula VI is outlined below NO2 NO2 H x NH2 H x Ro 0 F Base RO 0 N,..
\1,1 reduction . Ro 40 n F y F F y F
F H2N,,../x F
I
jI III IV
Y
II (11 IPyridine protection R-1¨C1 or Et3N, CH2Cl2 0 v 0\ 0 0 0\ /0 H /2 R--S-,?
R =N
N--'( N¨\ H
, X N,,,,./X N X
Ro 0 Et3N, CH2C12 RO
.1 I
,. 0 Ro 1.1 j NaOH ' F
F y H F Y Y
F
R¨ F
R¨-Cl F
VII VIII VI
V
Scheme I above illustrates the preparation of sulfonamide derivatives of formula VI.
1,2 Diamine derivative (formula IV) can be easily prepared in two steps from the desired nitro derivatives (formula I). Compounds of formula IV can be reacted with the sulfonyl chloride derivatives (formula V, see next scheme) to form the desired sulfonamide.
Alternatively, the 1,2 diamine derivatives IV can be protected to for an imidazolidone (formula VII), before being reacted with the corresponding sulfonyl chloride.
Deprotection of the 1,2 diamine VIII under basic conditions provided the desired material VI.
II. The general route to synthesis compound of general formula V is outlined below R
CI n-BuOH t\ S 0 RBr ____________________ N 0Bu S 0Bu pyridine % n-BuLi ,.% %
IX )0( XI
R R
KSCN >LOK SOCl2 ., XII V
Scheme II above shows one example of the preparation of complex sulfonyl chloride.
Compound XX can be synthesized from IX, alkylated, and converted to the potassium salt XII. Treatment of the salt with SOC12 or POC13 affords the desired compounds.
Other more specific procedures to prepare unique sulfonyl chloride derivatives are reported in the experimental section.
The following examples are provided so that the invention might be more fully understood.
These examples are illustration of the scope of the invention only and should not be construed as limiting the invention in any way.
Typical procedures for the synthesis of sulfonamides:
Procedure A: To a solution of the amine (1 eq) in anhydrous dichloromethane (3 mL/
mmole) was added anhydrous triethylamine (5 eq). To this solution was added the sulfonyl chloride (1 eq) and the solution was stirred at room temperature for 16 h. The solvent was evaporated and the residue was purified by flash column chromatography on silica.
Procedure B: To a stirred solution of the amine (1 eq) in anhydrous pyridine (5m1/mmole) was added the sulfonyl chloride (1 - 5 eq). The reaction mixture was stirred at 40 C for 48 hours. The reaction mixture was partitioned with water and Et0Ac. The organic layer was washed with brine, dried (MgSO4) and concentrated under reduced pressure. The residue was purified by flash column chromatography on silica.
Example 1 N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)phenyl)methanesulfonamide:
Step A: 2,3-Difluoro-N-(2-fluoro-4-iodopheny1)-6-nitroaniline:
N (101 To a solution of 2-fluoro-4-iodoaniline (11.40 g, 47 mmol) in 100 ml anhydrous THF
at 0 C, 47 ml of a 1M solution of LHMDS in THF (47 mmol) was added dropwise.
The color of the solution turned dark purple. The solution was transferred via cannula to a dropping funnel, and the solution (containing the amine free base) was added in small portions to a solution of 2,3,4-trifluoronitrobenzene (8.321 g, 47.0 mmol) in anhydrous THF
(50 ml) at 0 'C. After completion of addition the mixture was stirred under argon at room temperature for 15 hours. The volume of the solvent was reduced, followed by extraction using ethyl acetate and brine. The organic layer was dried over sodium sulfate, the solvent was removed, and the obtained dark oil was purified by flash chromatography (Et0Ac /
hexane 1:5, Rf = 0.58) yielding the crude product, which became a brown solid upon drying in vacuo (yield: 6.23 g, 33.6%). m/z = 393 EM-if.
Step B: 5,6-Difluoro-N1-(2-fluoro-4-iodophenyl)benzene-1,2-diamine To a solution of nitro-diarylamine (6.23 g, 15.8 mmol) in 300 ml ethanol was added iron powder (13.74 g, 246 mmol) and ammonium chloride (13.59 g, 254 mmol) and the mixture was heated with stirring at 100 C oil bath temperature for 14 hours.
It was filtered and the residue washed two times with ethanol. The ethanol was removed in vacuo, and the residue was extracted using ethyl acetate / 1M NaOH solution. During the extraction, more precipitate was formed which was filtered and discarded. The combined organic layers were washed with brine and dried over sodium sulfate. The solvent was removed, and the crude product was recrystallized from CHC13 / hexane (1:50). The product was obtained as brown needles (2.094 g, 66%,). Rf = 0.44 (Et0Ac / Hex 1:3). 1H-NMR (500 MHz, CDC13):
5 = 7.40-7.38 (dd, 1H, J= 11.3 Hz, J= 1.5 Hz). 7.25-7.23 (d, 1H, J= 8.5 Hz), 6.97-6.92 (q, 1H, J= 9 Hz), 6.51-6.48 (m, 1H), 6.24-6.21 (t, 1H, J= 9 Hz), 5.3 (s, 1H, NH, br), 3.80 (s, 2H, NI-12, br); LRMS (ESI): nilz = 365 [M+Hr.
Step C: N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino) phenyl) methanesulfonamide:
0// 1\11-1 H F
N
OI
According to the general procedure A, 5,6-difluoro-N1-(2-fluoro-4-iodophenyl)benzene-1,2-diamine was reacted with methanesulfonyl chloride to obtain the desired product. 1HNMR: (500 MHz, CDC13): 8 = 7.38-7.37 (d, 111), 7.35-7.34 (m, 1H), 7.27-7.26 (m, 1H), 7.20-7.0 (q, 1H), 6.68 (s, 1H, br), 6.15-6.12 (q, 1H), 5.65 (s, 1H, br), 2.95 (s, 3H); in/z= 441 [M-11".
Example 2 N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)phenyl)cyclopropanesulfonamide:
N
According to the general procedure A, 5,6-difluoro-N1-(2-fluoro-4-iodophenyl) benzene-1,2-diamine was reacted with cyclopropanesulfonyl chloride to obtain the desired product. 1HNMR.: (500 MHz, CDC13): 8 = 7.38-7.37 (d, 1H), 7.35-7.34 (m, 1H), 7.27-7.26 (m, 1H), 7.20-7.0 (q, 1H), 6.68 (s, 1H, br), 6.15-6.12 (q, 1H), 5.65 (s, 1H, br), 3.25-3.20 (m, 1H), 2.4-2.3 (m, 2H), 2.0-1.8 (m, 2H); in/z = 467 [M-lf.
Example 3 N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)phenyl)propane-2-sulfonamide:
)s(,0 0/ 1µ1F1 El F
F I
F
According to the general procedure A, 5,6-difluoro-N1-(2-fluoro-4-iodophenyl)benzene-1,2-diamine was reacted with isopropylsulfonyl chloride to obtain the desired product. Yield: 39%. 1H-NMR (500 MHz, CDC13): 5 = 7.50-7.43 (m, 1H), 7.35-7.34 (m, 1H), 7.27-7.26 (m, 1H), 7.15-7.09 (q, 1H, J= 1.6 Hz), 6.62 (s, 1H, br), 6.22-6.18 (q, 1H, J= 1.5 Hz), 5.65 (s, 1H, br), 3.30-3.28 (in, 1H), 1.38-1.37 (d, 6H, J= 1.2 Hz); m/z = 469 [M-IT.
Example 4 N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)phenyl)butane-l-sulfonamide:
Fi F
F I
F
According to the general procedure A, 5,6-difluoro-N1-(2-fluoro-4-iodophenyl)benzene-1,2-diamine was reacted with n-butylsulfonyl chloride to obtain the desired product. Yield: 55%. 1H-NM (500 MHz, CDC13): 6 = 7.50-7.43 (in, 1H), 7.35-7.34 (m, 1H), 7.27-7.26 (m, 1H), 7.15-7.09 (q, 1H, J= 1.6 Hz), 6.62 (s, 1H, br), 6.22-6.18 (q, 1H, J= 1.5 Hz), 5.65 (s, 1H, br), 3.06-3.031 (t, 2H, J= 1.4 Hz), 1.75-1.71 (m, 2H), 1.38-1.36 (m, 2H), 0.87-0.86 (t, 3H, J= 1.3 Hz); rn/z = 483 [M-lf.
Example 5 N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)pheny1)-2,2,2-trifluoro ethane sulfonamide:
F3C,S(/
cy 'NH H F
N
According to the general procedure A, 5,6-difluoro-N1-(2-fluoro-4-iodophenyl)benzene-1,2-diamine was reacted with 1,1,1-trifluoroethylsulfonyl chloride to obtain the desired product. Yield: 28%. tn/z = 509 [M-lf.
Example 6 N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)phenyl)butane-2-sulfonamide:
s(/0 e 'NH H F
According to the general procedure A, 5,6-difluoro-N1-(2-fluoro-4-iodophenyl)benzene-1,2-diamine was reacted with sec-butylsulfonyl chloride to obtain the desired product. Yield: 22%. 1H-NMR (500 MHz, Me0H[d4]): 5 = 7.60-7.40 (m, 3H), 7.18-7.00 (q, 1H), 6.55-6.45 (m, 1H), 3.55-3.50 (m, 1H), 2.20-2.00 (m, 1H), 1.80-1.60 (m, 111), 1.43-1.40 (d, 3H), 1.06-1.04 (t. 3H); tn/z = 483 [m-if.
Example 7 N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)pheny1)-N-methyl cyclopropane sulfonamide:
ACo 'N H F
N
To a solution of N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)phenyl)cyclopropane-sulfonamide (see Example 2) (283.9 mg, 0.61 mmol) in 3 ml anhydrous THF was added at -78 C a 1M solution of LHMDS (0.6 ml, 0.6 mol) and the solution was stirred for 10 min at this temperature. Then, methyl iodide (0.8 ml, 1.824 g, 12.9 mmol) was added and the mixture was warmed to room temperature and stirred for 7 h. The solvent was removed and the residue extracted using EtAc and brine. The organic fractions were dried using Na2SO4 and the solvent was removed. The obtained crude product was purified using flash-column chromatography (Si, EtAc/Hexanes 1:2, Rf = 0.45). Yield: 205 mg, 70%). 1H-NMR (500 MHz, CDC13): 5 =
7.41-7.39 (d, 1H, J = 10 Hz), 7.30-7.29 (d, 1H, J = 8.0 Hz), 7.23-7.20 (m, 1H), 6.98-6.93 (q, 1H, J = 8.5 Hz), 6.60 (s, 1H, br), 6.51-6.47 (m, 1H), 3.23 (s, 3H), 2.46-2.42 (m, 1H), 1.19-1.16 (m, 2H), 1.04-1.02 (m, 2H); in/z¨ 481 [M-lf.
Example 8 1-Chloro-N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)phenyl) methane sulfonamide:
CI
cy NH Ei F
N
According to the general procedure A, 5,6-difluoro-N1-(2-fluoro-4-iodophenyl)benzene-1,2-diamine was reacted with chloromethanesulfonyl chloride to obtain the desired product. m/z = 475 rm-ir.
Example 9 N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)pheny1)-2-methylpropane-2-sulfonamide:
g ll'NH H F
=
la F I
F
According to the general procedure B, 5,6-difluoro-N1-(2-fluoro-4-iodophenyl)benzene-1,2-diamine was reacted with 2-methylpropane-2-sulfonyl chloride 5 (synthesized according to the literature procedure) to obtain the desired product. 1H NMR
(300 MHz, CDC13): 6 7.50 (m, 1H), 7.43 (dd, J= 1.8 & 10.5 Hz, 1H), 7.28 (br s, 1H), 7.10 (dd, J= 9.0 & 17.7 Hz, 1H), 6.48 (br s, D20 exchangeable, 1H), 6.19 (t, J= 7.8 & 9.6 Hz, 1H), 5.58 (br s, D20 exchangeable, 1H), 1.39 (s, 9H); m/z = 383 [M-lf.
10 Example 10 N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)phenyl)cyclopentanesulfonamide:
V, 0-- 8 NH Ed F
'FOP
F
According to the general procedure B, 5,6-difluoro-N1-(2-fluoro-4-iodophenyl)benzene-1,2-diamine was reacted with cyclopentanesulfonyl chloride to obtain the desired product1H NMR (300 MHz, CDC13): 6 7.42 (dd, J= 2.1 & 10.5 Hz, 1H), 7.36 (ddd, J= 2.4, 4.8, & 9.3 Hz, 1H), 7.25 (m, 2H), 7.10 (dd, J= 9.6 & 17.7 Hz, 1H), 6.67 (br s, D20 exchangeable, 1H), 6.20 (dt, J= 1.5, 8.4 & 17.4 Hz, 1H), 3.53 (p, 1H), 1.80 (m, 8H); m/z = 495 EM-if.
Example 11 N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)phenyl)cyclohexanesulfonamide:
H
0s, ,8 NH id F
lei lel F I
F
According to the general procedure B, 5,6-difluoro-N1-(2-fluoro-4-iodophenyObenzene-1,2-diamine was reacted with cyclohexanesulfonyl chloride to obtain the desired product. 1HNMR (300 MHz, CDC13): 5 7.43 (dd, J=1.5 & 10.2 Hz, 1H), 7.37 (ddd, J= 2.4, 4.8 & 9.6 Hz, 1H), 7.27 (m, 111), 7.11 (dd, J= 9.3 & 18.0 Hz, 1H), 6.64 (br s, 1H), 6.18 (dt, J= 1.5, 9.0 & 17.4 Hz, 1H), 5.63 (br s, 1H), 2.95 (triplet of triplet, 2.10-1.16 (m, 10H); rn/z = 509 [M-lf.
Example 12 N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)pheny1)-1-methylcyclopropane-1-sulfonamide:
Step A: n-Butyl 3-chloro-1-propanesulfonate:
CIS'C) o' 0-nBu Triethylamine (28 ml, 200 mmol) in CH2C12 (50 ml) was slowly added to an ice-cooled solution of 3-chloro-1-propanesulfonyl chloride (36.6g, 200 mmol) and 1-butanol (18.4 g, 240 m mol) in CH2C12 (250 ml) and stirring was continued for 16h. The mixture was diluted with CH2C12 (200 ml), washed (aqueous HC1) and dried (MgSO4) and the solvent was evaporated to obtain the titled product 1 (40.85 g, 95%) in crude form as slightly yellow oil which was used for the next reaction without further purification. III NMR
(CDC13)) 5 0.94 (t, J = 7.5 Hz, 3H), 1.44 (sextet, 2H), 1.72 (quintet, 2H), 2.31(quintet, 2H), 3.27(t, J = 6.9 Hz, 2H), 3.68 (t, J = 6.3 Hz), 4.23 (t, J = 6.6 Hz, 2H).
Step B: 1-Butyl cyclopropanesulfonate:
so 0-nBu Solutions of 1-butyl 3-chloro-1-propanesulfonate (4.6 g, 21.39 mmol in 25 ml THF) and of butyllithium (14.7 ml, 23.53 mmol, 1.6M, THF) were simultaneously added to THF
(150 ml) at -78 C under nitrogen atmosphere. The solution was allowed to warm to 0 C and then quenched with water (2 m1). The volatiles evaporated under reduced pressure and the residue extracted with CH2C12 (150 m1). The extract was washed with water and dried (MgSO4) and evaporated to give crude desired product (3.23 g, 78.22%) in almost pure form as pale yellow oil which was used for next step without further purification.
1H NMR (300 MHz, CDC13) 6 0.94 (t, J = 7.5 Hz, 3H), 1.07 (m, 2H), 1.25 (m, 2H), 1.45(sextet, 2H), 1.74(quintet, 2H), 2.45 (heptet, 1H), 4.23 (t, J = 6.6 Hz, 2H).
Step C: Butyl 1-Methyl-cyclopropanesulfonate:
'6"Q, O'Y-0-nBu To a solution of 1-Butyl cyclopropanesulfonate (1 g, 5.58 mmol) in THF (15 ml) butyllithium solution ( 3.84 ml, 6,14 mmol, 1.6M, THF) was slowly added at -78 C under nitrogen atmosphere. After 15 minutes Mel (0.72 ml, 11.16 mmol) was added and the solution was allowed to warm to 0 C and quenched with water (1 m1). The volatiles evaporated under reduced pressure and the residue extracted with CH2C12 (100 m1). The extract was washed with water, dried (MgSO4) and evaporated. The residue was purified over silica gel chromatography (eluants: hexane/ CH2C12) to obtain the titled product (0.59 g, 55.0%) as a colorless oil. 1H NMR (300 MHz, CDC13)) 6 0.84 (m, 2H), 0.95 (t, J
= 7.2 Hz, 3H), 1.43 (m, 4H), 1.53 (s, 3H), 1.74(m, 2H), 4.21 ((t, J = 6.6 Hz, 2H).
Step D: 1-Potassium 1-Methyl-cyclopropanesulfonate:
OK
A mixture of 1- Butyl 1-Methyl-cyclopropanesulfonate (0.386 g, 2 mmol) and potassium thiocyanate (0.194 g, 2 mmol) in DME (5 ml) and water (5 ml) was refluxed for 16h. The volatiles were evaporated to obtain the crude sulfonate (0.348g, quantitative) which was dried under vacuum at 50 C for 16h. The crude product was used in the next reaction without further purification. NMR (300 MHz, D20) 5 0.56 (t, J = 6.3 Hz, 2H), 0.96 (t, J =
6.3 Hz, 2H), 1.26 (s, 3H).
Step E: 1-Methyl-cyclopropanesulfonylchloride:
CI
A solution of 1-potassium 1-methyl-cyclopropanesulfonate (0.348 g, 2 mmol), thionyl chloride (5 ml) and DMF (5 drops) was refluxed at 60 C for 16h. The volatiles evaporated under reduced pressure and the residue extracted with CH2C12 (50 m1). The extract was washed with water, dried (MgSO4) and evaporated to obtain the crude product as yellow gummy oil which was used in the next reaction without further purification.
Step F: N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)pheny1)-1-methylcyclopropane-1-sulfonamide:
_II 'NH H F
la lel According to the general procedure B, 5,6-difluoro-N1-(2-fluoro-4-iodophenyl)benzene-1,2-diamine was reacted with 1-methyl-cyclopropanesulfonylchloride to obtain the desired product. 1H NMR (300 MHz, CDC13): 8 7.42 (dd, J= 1.8 & 10.5 Hz, 1H), 7.36 (ddd, J= 2.4, 4.5 & 9.0 Hz, 1H), 7.27 (d, J= 6.0 Hz, 1H), 7.07 (dd, J=
9.3 & 17.7 Hz, 1H), 6.24 (dt, J= 2.1, 8.7 & 17.4 Hz, 1H), 5.86 (br s, 1H), 1.43 (s, 3H), 1.33 (t, J= 5.4 Hz, 2H), 0.75 (dd, J= 5.1 & 6.3 Hz, 2H); m/z = 481 {M-lf.
Example 13 N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)pheny1)-1-(2,3-dihydroxypropyl) cyclopropane-l-sulfonamide:
Step A: Butyl cyclopropanesulfonate:
Aõ.
sO
Cyclopropanesulfonyl chloride (5 g, 35 mmole, 1 eq) was dissolved in an excess BuOH (20 ml), the reaction mixture was cooled at -10 C and pyridine (5.8 mL, 70 mmole, 2 eq) was slowly added dropwise. The mixture was slowly warmed at room temperature and stirred overnight. The solvent was removed under reduced pressure and the resulting white solid was dissolved in CHC13. The organic phase was washed with water, brine and dried (MgSO4) and concentrated to give an oil (4.8 g, 24.9 mmole, 71%). 1HNMR (300 MHz, CDC13): 8 4.25 (t, 2H), 2.46 (m, 1H), 1.74 (m, 2H), 1.45 (m, 2H), 1.25 (dd, 2H), 1.09 (dd, 2H), .93 (t, 3H).
Step B: Butyl 1-allylcyclopropane-1-sulfonate:
r, To a solution of 1-butyl cyclopropanesulfonate (4.8 g, 24.9 mmole) in THF at -78 C was added simultaneously butyllithium solution (15. 6 ml, 24.9 mmol, 1.6M, THF) and ally!
iodide (24.9 mmole) under nitrogen atmosphere. The reaction mixture was stirred 2 hours at -78 C and 3 hours at room tempoerature. The volatiles were evaporated under reduced pressure and the residue extracted with CH2C12 (100 m1). The extract was washed with water, dried (MgSO4) and evaporated. The residue was purified over silica gel chromatography (eluants: hexane/ CH2C12) to obtain the titled product (3.75 g, 69.0%) as a colorless oil. Ili NMR (300 MHz, CDCI3): 5 5.6 (m, 1H), 5.13-5.08 (t, 2H), 4.21 (t, 2H), 2.65 (d, 2H), 1.7 (m, 2H), 1.4 (in, 4H), .93 (m, 5H).
Step C: Potassium 1-allylcyclopropane-1-sulfonate:
AlrO-K+
S, d/ \O
A mixture of 1- butyl 1-methyl-cyclopropanesulfonate (3.75 g, 17.2 mmol) and potassium thiocyanate (1.7 g, 17.2 mmol) in DME (20 ml) and water (20 ml) was refluxed for 16h. The volatiles were evaporated to obtain the crude sulfonate (3.44g, quantitative) which was dried under vacuum at 50 C for 16h. The crude product was used in the next reaction without further purification. 1H NMR (CDC13): 5 5.6 (m, 1H), 4.91-4.85 (dd, 2H), 2.471-2.397 (d, 2H), 0.756 (m, 2H), 0.322 (m, 2H).
Step D: 1-allylcyclopropane-1-sulfonyl chloride:
LKICI
S
0/' A solution of potassium 1-allylcyclopropane-1-sulfonate (3.44 g, 17.2 mmol), thionyl chloride (10 ml) and DMF (5 drops) was refluxed at 60 C for 16h. The volatiles evaporated under reduced pressure and the residue extracted with CH2C12 (50 m1). The extract was washed with water, dried (MgSO4) and evaporated to obtain the crude product as yellow gummy oil which was washed with hexane and used in the next reaction without further purification (2.7 g, 15 mmole, 87%). 111 NMR (300 MHz, CDC13): 5 5.728 (m, 1H), 5.191 (t, 2H), 2.9 (d, 2H), 0.756 (m, 2H), 0.322 (m, 2H).
Step E: 1-allyl-N-(3,4-difluoro-2-(2-fluoro-4-iodophenvlamino)phenyl)cyclopropane-1-sulfonamide:
FOI
According to the general procedure B, 5,6-difluoro-N1-(2-fluoro-4-iodophenyl)benzene-1,2-diamine was reacted with 1-allylcyclopropane-1-sulfonyl chloride to obtain the desired product. m/z = 507 [M-ir.
Step F: N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)pheny1)-1-(2,3-dihydroxypropyl)cyclopropane-1-sulfonamide:
õ31,15q HO
H'NH H F
1-Allyl-N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino) phenyl)cyclopropane-1-sulfonamide ( 0,77 g, 1.52 mmole) and 4-methylmorpholine N-oxide (0,18 g, 1.52 mmole) were dissolved in THF (50 mL). Osmium tetroxide was added at room temperature (0.152 mmole, 0.965 mL, 4% in H20) and the reaction mixture was stirred at room temperature for 16 hours. Et0Ac was added, the organic phase was washed with water, dried (MgSO4) and concentrated under reduced pressure. The residue was purified over silica gel chromatography (eluants: Et0Ac/ Me0H) to obtain the titled product (0. 65 g, 79%). Ili NMR (300 MHz, CDC13 + D20): 8 7.38 (dd, J= 1.8 & 10.5 Hz, 1H), 7.36 (ddd, J=
2.4, 5.1 & 9.3 Hz, 1H), 7.25 (d, J= 8.7 Hz, 1H), 7.02 (dd, J= 9.0 & 17.7 Hz, 1H), 6.27 (dt, J= 3.0, 8.7 & 17.4 Hz, 1H), 3.92 (m, 1H), 3.54 (dd, J= 3.9 & 11.1 Hz, 1H), 3.39 (dd, J= 6.6 & 11.1 Hz, 1H), 2.16 (dd, J= 9.6 & 15.9 Hz, 1H), 1.59 (d, J= 14.1 Hz, 1H), 1.41 (m, 1H), 1.26 (m, 1H), 0.83 (m, 2H); m/z = 542 [M-1]..
Example 14 (S)-N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)pheny1)-1-(2,3-dihydroxypropyl)cyclopropane-1-sulfonamide:
HO
NH H F
The pure S isomer was obtained by chiral HPLC separation of the racemic mixture (example 13). 'H NMR (300 MHz, CDC13+ D20): 8 7.38 (dd, J= 1.8 & 10.5 Hz, 1H), 7.36 (ddd, J= 2.4, 5.1 & 9.3 Hz, 1H), 7.25 (d, J= 8.7 Hz, 1H), 7.02 (dd, J= 9.0 &
17.7 Hz, 1H), 6.27 (dt, J= 3.0, 8.7 & 17.4 Hz, 1H), 3.92 (m, 1H), 3.54 (dd, J= 3.9 & 11.1 Hz, 1H), 3.39 (dd, J= 6.6 & 11.1 Hz, 1H), 2.16 (dd, J= 9.6 & 15.9 Hz, 1H), 1.59 (d, J= 14.1 Hz, 1H), 1.41 (m, 1H), 1.26 (m, 1H), 0.83 (m, 2H); m/z = 542 D.4-1f.
Example 15 (R)-N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)pheny1)-1-(2,3-dihydroxypropyl)cyclopropane-1-sulfonamide:
OH v-7 1-1'NH H F
1.1 The pure R isomer was obtained by chiral HPLC separation of the racemic mixture (example 13). IH NMR (300 MHz, CDC13 + D20): 67.38 (dd, J= 1.8 & 10.5 Hz, 1H), 7.36 (ddd, J= 2.4, 5.1 & 9.3 Hz, 1H), 7.25 (d, J= 8.7 Hz, 1H), 7.02 (dd, J= 9.0 &
17.7 Hz, 1H), 6.27 (dt, J= 3.0, 8.7 & 17.4 Hz, 1H), 3.92 (m, 1H), 3.54 (dd, J= 3.9 & 11.1 Hz, 1H), 3.39 (dd, J= 6.6 & 11.1 Hz, 1H), 2.16 (dd, J= 9.6 & 15.9 Hz, 1H), 1.59 (d, J= 14.1 Hz, 1H), 1.41 (m, 1H), 1.26 (m, 1H), 0.83 (m, 2H); nilz = 542 [M-lf.
Example 16 N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)pheny1)-1-(2-hydroxyethyl)cyclopropane-l-sulfonamide:
Step A: 2-(1-bromocyclopropyl)ethanol:
Br OH
To a solution of neat diethyl zinc (3.3 ml, 3.977 g, 30 mmol) in 100 ml anhydrous DCM was added very slowly trifluoroacetic acid (2.31 ml, 3.4188 g, 30 mmol) dropwise at 0 C. (Caution: Violent gas evolution, exothermic!). After completed addition of the TFA, the suspension was stirred for 20 min at the same temperature, followed by the addition of diiodo methane (2.45 ml, 8.134 g, 30.4 mmol). It was further stirred at 0 C for 20 min, and then a solution of 3-bromobut-3-en-1-ol (1 ml, 1.523 g, 10.1 mmol) in 10 ml DCM was added at the same temperature. After complete addition, the mixture was warmed to room temperature and stirred for 4 hours. The mixture was quenched with 100 ml Me0H and 40 ml brine, and it was further stirred for 30 min. The solvents were reduced, and the residue extracted using CHC13 / aq. NH4C1. The organic layers were collected, washed with brine and water, and the solvent was removed to give 2-(1-bromocyclopropy1)-ethanol in sufficient purity (1.6564 g, 100%). 1H-NMR (500 MHz, CDCI3): 8 = 3.90-3.83 (t, 2H), 1.91-1.87 (t, 2H), 1.71 (s, 1H, br), 1.14-1.09 (m, 2H), 0.83-0.79 (m, 2H).
Step B: TBS protected 2-(1-bromocyclopropyl)ethanol:
Br OTBS
To a solution of the cyclopropyl alcohol (Step A) (1.303 g, 7.95 mmol) in 30 ml anhydrous DCM was added anhydrous pyridine (1.2 ml, 1,1736 g, 14.8 mmol) and TBSOTf (2.7 ml, 3.1077 g, 11.76 mol) and the solution was stirred at room temperature for 16 h. It was extracted with CHCI3 / brine and the organic fraction was dried with MgSO4. The solvent was reduced and the crude product purified using flash-column chromatography (Si, CHC13 /
hexanes 1:10, Rf 0.4). Yield: 0.796 g, 36%. 'H-NMR (500 MHz, CDC13): 8 = 3.95-3.75 (t, 2H), 1.95-1.85 (t, 2H), 1.15-1.05 (m, 2H), 0.95-0.80 (m, 11H), 0.15-0.05 (s, 6H).
Step C: TBS protected 2-(1-chlorosulfonylcyclopropyl)ethanol:
OTBS
To a solution of the cyclopropyl bromide prepared in step B (1.1227 g, 4.04 mmol) in ml anhydrous diethyl ether was added a 1.7 M solution of t-BuLi in pentane (4.8 ml, 8.16 15 mmol) at ¨ 78 C. The solution was stirred for 30 min at this temperature, and was then transferred via a transfer canola into a solution of freshly distilled sulfuryl chloride (0.65 ml, 1.029 g, 8.1 mmol) in 8 ml diethyl ether at ¨ 78 C. The yellow suspension was warmed to room temperature. The solvent was removed, and the residue was dried in vacuo to remove excessive sulfuryl chloride. Then, the residue was extracted two times with hexane, and after filtration the solvent was evaporated in vacuo to give the sulfonyl chloride in sufficient purity as a colorless oil. Yield: 870 mg (72%). 1H-NMR (300 MHz, CDC13): 6 = 3.95-3.85 (t, 2H), 2.35-2.25 (t, 2H), 1.80-1.70 (m, 2H), 1.45-1.38 (m, 2H), 0.90 (s, 9H), 0.10 (s, 6H).
Step D: TBS-protected N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)pheny1)-1-(2-hydroxyethyl)cyclopropane-l-sulfonamide:
(OTBS
N
OI
According to the general procedure B, 5,6-difluoro-N1-(2-fluoro-4-iodophenyl)benzene-1,2-diamine was reacted with the cyclpropylsulfonyl chloride prepared in step C to obtain the desired product. 1H-NMR (300 MHz, CDC13): 5 = 7.44-7.39 (dd, 1H), 7.32-7.24 (m, 2H), 7.1-6.98 (q, 1H), 6.34-6.24 (m, 1H), 6.16 (s, 1H, br), 3.85-3.75 (t, 2H), 2.15-2.00 (t, 2H), 1.35-1.20 (m, 2H), 0.95-0.75 (m, 11H), 0.10 (s, 6H); in/z = 625 [Mir.
Step E: N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)pheny1)-1-(2-hydroxyethyl)cyclopropane-l-sulfonamide:
(OH
Alk/e0 cy NH H F
N
To a solution of the TBS-protected sulfonamide prepared in step D (21 mg, 0.033 mmol) in 1 ml THF was added 0.1 ml aq.1.2N HC1 solution at 0 C and the solution was stirred for 2 h.
The solvents were reduced and the residue was extracted using aq. NaHCO3 solution and EtAc.
The organic fractions were dried with MgSO4 and the volatiles were removed.
The crude product was purified using flash-column chromatography (Si, CHC13 / Me0H 10:1, R, = 0.45) to give the pure product. Yield: 16.9 mg (100%). 1H-NMR (300 MHz, CDCI3): 5 =
7.44-7.39 (dd, 1H), 7.32-7.24 (m, 2H), 7.1-6.98 (q, 1H), 6.34-6.24 (m, 1H), 6.16 (s, 1H, br), 3.85-3.75 (t, 2H), 2.15-2.00 (t, 2H), 1.35-1.20 (m, 2H), 0.95-0.85 (m, 2H); m/z = 511 [M-lf.
Example 17 N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)pheny1)-3-hydroxypropane-1-sulfonamide:
II
HO (3 NH H F
To a solution of 3-Chloro-N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)pheny1)-propane-1-sulfonamide (69.4 mg, 0.138 mmol) in a mixture of 8 ml 1,4-dioxane and 2 ml H20 was added KOH powder (0.674 g, 12.0 mmol) and the mixture was heated to the reflux temperature for 3 days. It was extracted using EtAc / brine, the organic fraction was dried with Na2SO4 and 10 the volatiles were removed. The residue was purified using flash-column chromatography (Si, DCM / Me0H 5:1, Rf = 0.3). Yield: 41 mg (62%). 1H-NMR (500 MHz, Me0H [d4]): 6 = 7.38-7.21 (d, 1H), 7.23-7.21 (d, 1H), 7.06-7.00 (q, 1H), 6.52-6.50 (m, 1H). 6.17-6.13 (t, 1H), 3.30-3.27 (t, 2H), 2.86-2.83 (t, 2H), 2.05-2.00 (m, 2H); m/z = 485 [m-if.
Example 18 N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)pheny1)-2-methyl-5-(trifluoromethyl)furan-3-sulfonamide:
1;) 0'NH
According to the general procedure 5,6-difluoro-N1-(2-fluoro-4-iodophenyl)benzene-1,2-diamine (0.182 mmole) was reacted with 2-methyl-5-(trifluoromethyl)furan-3-sulfonyl chloride (0.5 mmole) to form N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)pheny1)-2-methyl-5-(trifluoromethyl)furan-3-sulfonamide. 1H NMR (CDC13) 5 2.2 (s, 3H), 5.3 (s, 1H), 6.0 (dt, 1H), 6.8 (s, 114), 6.95 (s, 1H), 7.0-7.3 (m, 3H), 7.4 (dd, 1H).
Example 19 N-(5-(N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)phenyl)sulfamoy1)-methylthiazol-2-yl)acetamide:
HN
0'NH
la 40 According to the general procedure 5,6-difluoro-N1-(2-fluoro-4-iodophenyObenzene-1,2-diamine (0.182 mmole) was reacted with 2-acetamido-4-methylthiazole-5-sulfonyl chloride (0.5 mmole) to obtain N-(5-(N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)phenypsulfamoy1)-4-methylthiazol-2-ypacetamide . 1H NMR
(CDC13)) 2.1 (s, 3H), 2.2 (s, 3H), 5.9 (dt, 1H), 6.05 (s, 1H), 7.0-7.6 (m, 3H), 7.4 (dd, 1H), 8.0 (s, 1H).
Example 20 5-(5-Chloro-1,2,4-thiadiazol-3-y1)-N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino) phenyl) thiophene-2-sulfonamide:
CI
o N
0'NH
According to the general procedure 5,6-difluoro-N1-(2-fluoro-4-iodophenyl)benzene-1,2-diamine (0.182 mmole) was reacted with 5-(5-chloro-1,2,4-thiadiazol-3-yl)thiophene-2-sulfonyl chloride (0.5 mmole) to obtain 5-(5-chloro-1,2,4-thiadiazol-3-y1)-N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)phenyl)thiophene-2-sulfonamide. 1H NMR (300 MHz, CDC13)) 8 5.8 (dt, 1H), 5.95 (s, 1H), 6.95 (d, 1H),7.4 (m, 2H), 7.6 (d, 1H), 7.8 (s, 1H).
Example 21 N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)pheny1)-3,5dimethylisoxazole-4-sulfonamide:
N, ?
OX--\
0'NH
According to the general procedure 5,6-difluoro-N1-(2-fluoro-4-iodophenyl) benzene-1,2-diamine (0.182 mmole) was reacted with 3,5-dimethylisoxazole-4-sulfonyl chloride (0.5 mmole) to obtain N-(3,4-difluoro-2-(2-fluoro-4-iodophenyl amino)pheny1)-3,5dimethylisoxazole-4-sulfonamide. 1H NMR (300 MHz, CDC13)) 8 2.2 (s, 3H), 2.4 (s, 3H), 5.8 (s, 1H), 6.0 (dt, 1H), 5.95 (s, 111), 6.9 (s, 1H),7.0 (q, 1H), 7.2 (m, 3H), 7.4 (dd, 1H).
Example 22 5-Chloro-N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)pheny1)-1,3-dimethyl-1H-pyrazole-4-sulfonamide:
Nõ
Si According to the general procedure 5,6-difluoro-N1-(2-fluoro-4-iodophenyl) benzene-1,2-diamine (0.182 mmole) was reacted with 5-chloro-1,3-dimethy1-1H-pyrazole-4-sulfonyl chloride (0.5 mmole) to obtain 5-chloro-N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino) phenyl)-1,3-dimethy1-1H-pyrazole-4-sulfonamide. 1H NM-R (300 MHz, CDC13)) 5 2.1 (s, 3H), 3.6 (s, 3H), 5.8 (s, 1H), 5.95 (dt, 1H), 7.0 (q, 1H), 7.2 (d, 1H),7.3 (m, 2H), 7.4 (dd, 1H).
Example 23 N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)pheny1)-2,5-dimethylfuran-3-sulfonamide:
0,.....--0'NH F
H
N
lei 110 F I
F
According to the general procedure 5,6-difluoro-N1-(2-fluoro-4-iodophenyl) benzene-1,2-diamine (0.182 mmole) was reacted with 2,5-dimethylfuran-3-sulfonyl chloride (0.5 mmole) to obtain N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino) pheny1)-2,5-dimethylfuran-3-sulfonamide. 1H NMR (300 MHz, CDC13)) 8 2.2 (s, 3H), 2.3 (s, 3H), 5.8 (s, 1H), 6.0 (dt, 1H), 6.8 (s, 1H), 7.0 (q, 1H), 7.2 (d, 1H),7.3 (m, 2H), 7.4 (dd, 1H).
Example 24 N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)pheny1)-1-methy1-3-(trifluoromethyl)-1H-pyrazole-4-sulfonamide:
NI,Ni..
F3C-yIC:
H
N
Si la F I
F
According to the general procedure 5,6-difluoro-N1-(2-fluoro-4-iodophenyl) benzene-1,2-diamine (0.182 mmole) was reacted with 1-methy1-3-(trifluoromethyl)-1H-pyrazole-4-sulfonyl chloride (0.5 mmole) to obtain N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)pheny1)-1-methy1-3-(trifluoromethyl)-1H-pyrazole-4-sulfonamide. 1H
NMR (300 MHz, CDCI3)) 6 3.8 (s, 3H), 5.7 (s, 1H), 6.0 (dt, 1H), 7.0 (q, 1H), 7.2 (m, 2H), 7.4 (dd, 1H),7.8 (s, 1H).
Example 25 N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)pheny1)-2,4-dimethylthiazole-5-sulfonamide:
S)N
CO"---0..SNH F
H
N
F I
F
According to the general procedure 5,6-difluoro-N1-(2-fluoro-4-iodophenyl) benzene-1,2-diamine (0.182 mmole) was reacted with 2,4-dimethylthiazole-5-sulfonyl chloride (0.5 mmole) to obtain N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)phenyI)-2,4-dimethylthiazole-5-sulfonamide. 111 NMR (300 MHz, CDC13)) 6 2.3 (s, 3H), 2.6 (s, 3H), 5.7 (s, 1H), 5.9 (dt, 1H), 7.1 (q, 1H), 7.2 (d, 1H), 7.3 (m, 1H),7.4 (d, 1H), 7.4 (s, 111).
Example 26 N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)pheny1)-1,2-dimethy1-1H-imidazole-4-sulfonamide:
N\
1:Dr N
According to the general procedure B, 5,6-difluoro-N1-(2-fluoro-4-iodophenyObenzene-1,2-diamine was reacted with 1,2-dimethy1-1H-imidazole-4-sulfonyl chloride to obtain the title compound. 1H NMR. (300 MHz, CDC13): 6 7.95 (br s, 1H), 7.37 (dd, J= 1.8 & 10.8 Hz, 1H), 7.32-7.14 (m, 3H), 6.98 (dd, J= 9.6 & 17.7 Hz, 1H), 5.87 (dt, J
= 4.2, 9.0 & 17.4 Hz, 1H), 5.55 (br s, 1H), 3.49 (s, 3H), 2.31 (s, 3H).
Example 27 N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)phenyl)thiophene-3-sulfonamide:
g, S ONO
According to the general procedure B, 5,6-difluoro-N1-(2-fluoro-4-iodophenyl) benzene-1,2-diamine was reacted with thiophene-3-sulfonyl chloride to obtain the title compound. 1H NMR (300 MHz, CDC13): 6 8.00 (dd, J= 1.2 & 3.3 Hz, 1H), 7.45 (dd, J= 0.9 & 5.1 Hz, 1H), 7.35 (m, 2H), 7.27 (m, 2H), 6.91 (dd, J= 9.3 & 17.1 Hz, 1H), 6.64 (ddd, J=
2.1, 4.8 & 8.7 Hz, 1H), 6.34 (dt, J= 5.4, 8.7 & 14.1 Hz, 1H), 5.98 (br d, J=
2.1 Hz, D20 exchangeable, 1H).
Example 28 N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)phenyl)furan-2-sulfonamide:
According to the general procedure B, 5,6-difluoro-N1-(2-fluoro-4-iodophenyl)benzene-1,2-diamine was reacted with furan-2-sulfonyl chloride to obtain the title 5 compound. 1H NMR (300 MHz, CDC13): 8 7.53 (br s, D20 exchangeable, 1H), 7.38 (dd, J-1.8 & 10.5 Hz, 1H), 7.30 (d, J= 8.4 Hz, 1H), 7.21 (d, J= 3.0 Hz, 1H), 6.96 (dd, J= 8.7 &
16.5 Hz, 1H), 6.87 (ddd, J= 1.8, 5.1 & 9.0 Hz, 1H), 6.53 (dd, J= 1.8 & 3.6 Hz, 1H), 6.44 (dt, J= 5.1, 8.7 & 13.8 Hz, 1H), 6.22 (br s, D20 exchangeable, 1H).
10 Example 29 N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)pheny1)-5-methylthiophene-2-sulfonamide:
s s.
NH Fd F
According to the general procedure B, 5,6-difluoro-N1-(2-fluoro-4-iodophenyl)benzene-1,2-diamine was reacted with 5-methylthiophene-2-sulfonyl chloride to obtain the title compound. 1HNMR (300 MHz, CDC13): 8 7.34 (dd, .1= 0.9 & 10.2 Hz, 1H), 7.30 (ddd, J= 2.1, 4.8 & 9.0 Hz, 1H), 7.25 (d, J= 3.9 Hz, 1H), 7.07 (m, 2H), 6.65 (dd, J=
1.2 & 3.9 Hz, 1H), 5.89 (dt, J= 2.4, 8.7 & 17.4 Hz, 1H), 5.54 (br s, D20 exchangeable, 1H), 2.46 (s, 3H).
Example 30 5-Chloro-N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)phenyl)thiophene-2-sulfonamide:
S NH N F
\ / 0 H
According to the general procedure B, 5,6-difluoro-N1-(2-fluoro-4-iodophenyl)benzene1,2-diamine was reacted with 5-chlorothiophene-2-sulfonyl chloride to 5 obtain the title compound. 1H NMR (300 MHz, CDC13): 6 7.38 (dd, J=1.5 &
10.2 Hz, 1H), 7.32 (ddd, J= 2.1, 5.1 & 9.3 Hz, 1H), 7.25 (d, J= 3.9 Hz, 1H), 7.10 (dd, J=
9.0 & 18.6 Hz, 3H), 6.84 (d, J= 4.2 Hz, 1H), 5.86 (dt, J= 1.8, 8.7 & 17.4 Hz, 1H), 5.49 (br s, D20 exchangeable, 1H).
Example 31 5-Bromo-N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)phenyl)thiophene-2-sulfonamide:
SNH N F
\ / 0 H
According to the general procedure B, 5,6-difluoro-N1-(2-fluoro-4-iodophenyObenzene1,2-diamine was reacted with 5-bromothiophene-2-sulfonyl chloride to obtain the title compound. 1HNMR (300 MHz, CDC13): 6 7.39-7.29 (m, 2H), 7.20-7.05 (m, 3H), 6.96 (d, J= 3.6 Hz, 1H), 5.85(dt, J= 2.1, 9.0 & 17.4 Hz, 1H), 5.54 (br s, 1H).
Example 32 4-Bromo-N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)phenyl)thiophene-3-sulfonamide:
&(gl, / II NH
According to the general procedure B, 5,6-difluoro-N1-(2-fluoro-4-iodophenyObenzene1,2-diamine was reacted with 4-bromothiophene-3-sulfonyl chloride to obtain the title compound. 11-1NMR (300 MHz, CDC13): 8 7.48 (br m, 2H), 7.39 (dd, J= 1.8 & 10.5 Hz, 1H), 7.28 (ddd, J= 2.4, 4.8 & 9.0 Hz, 111), 7.17 (d, J= 8.4 Hz, 111), 7.02 (m, 1H), 6.02 (dt, J= 2.4, 8.7 & 17.4 Hz, 1H), 5.68 (br s, 1H).
Example 33 4-Bromo-5-chloro-N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)phenyl)thiophene-2-sulfonamide:
H F
Br According to the general procedure B, 5,6-difluoro-N1-(2-fluoro-4-iodophenyl)benzene1,2-diamine was reacted with 4-bromo-5-chlorothiophene-2-sulfonyl chloride to obtain the title compound. 1HNMR (300 MHz, CDC13): 8 7.42-7.34 (m, 2H), 7.25 (br m, 3H), 7.13 (dd, J= 9.0 & 17.1 Hz, 1H), 6.02 (dt, J= 2.4, 6.6 & 17.4 Hz, 1H), 5.52 (br s, 1H).
Example 34 3-Bromo-5-ehloro-N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino) phenyl)thiophene-2-sulfonamide:
CI s H F
Br 40 According to the general procedure B, 5,6-difluoro-N1-(2-fluoro-4-iodophenyl)benzene1,2-diamine was reacted with 3-bromo-5-chlorothiophene-2-sulfonyl chloride to obtain the title compound. 'H NMR (300 MHz, CDC13): 6 7.41 (dd, J=
2.1 & 10.5 Hz, 111), 7.35 (br m, 2H), 7.31 (dd, J= 2.1 & 4.2 Hz, 1H), 7.19 (d, J= 8.7 Hz, 1H), 7.08 (dd, J= 9.0 & 17.4 Hz, 1H), 6.02(dt, J= 2.1, 8.4 & 17.1 Hz, 1H), 5.59 (br s, 1H).
Example 35 N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)pheny1)-2,5-dimethylthiophene-3-sulfonamide:
N7S.
s 8 NH F
According to the general procedure B, 5,6-difluoro-N1-(2-fluoro-4-iodophenyl)benzene1,2-diamine was reacted with 2,5-dimethylthiophene-3-sulfonyl chloride to obtain the title compound. 1H NMR (300 MHz, CDC13): 6 7.39 (dd, J= 1.8 &
10.2 Hz, 1H), 7.24-7.16 (br m, 2H), 7.13 (dd, J= 9.0 & 17.4 Hz, 1H), 6.77 (d, J= 9.6 Hz, 1H), 5.98 (dt, J= 2.4, 8.7 & 17.4 Hz, 11-1), 5.55 (br s, 1H), 2.33 (s, 6H).
Example 36 2,5-Diehloro-N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)phenyl)thiophene-3-sulfonamide:
S ? / 8 NH H F
F I
F
According to the general procedure B, 5,6-difluoro-N1-(2-fluoro-4-iodophenyl)benzene1,2-diamine was reacted with 2,5-dichlorothiophene-3-sulfonyl chloride to obtain the title compound. 1HNMR (300 MHz, CDC13): 8 7.41(dd, J=1.5 & 10.5 Hz, 1H), 7.28-7.20 (m, 2H), 7.08 (dd, J= 9.0 & 17.4 Hz, 2H), 6.99 (s, 1H), 6.03 (dt, J=
2.1, 8.7 &
17.4 Hz, 1H), 5.56 (br s, 1H).
Example 37 Methyl 3-(N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)phenyl) sulfamoyl)thiophene-2-carboxylate:
sia/I.NH Fd F
Me02C 40 1110 F I
F
According to the general procedure B, 5,6-difluoro-N1-(2-fluoro-4-iodophenyl) benzene1,2-diamine was reacted with methyl 3-(chlorosulfonyl)thiophene-2-carboxylate to obtain the title compound. 1HNMR (300 MHz, CDC13): 8 8.58 (s, 1H), 7.43 (dd, J=5.1&
10.8 Hz, 2H), 7.35 (dd, J= 1.8 & 10.2 Hz, 1H), 7.31 (ddd, J= 2.1, 4.2 & 9.3 Hz, 1H), 7.04 (m, 2H), 5.88 (dt, J= 2.7, 8.7 & 17.4 Hz, 1H), 5.65 (br s, 1H), 3.85 (s, 3H).
Example 38 Methyl 5-(N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)phenyl)sulfamoy1)-1-methyl-1H-pyrrole-2-carboxylate:
yH, 9 Me02CO3 k N H'NH
According to the general procedure B, 5,6-difluoro-N1-(2-fluoro-4-iodophenyl)benzene1,2-diamine was reacted with methyl 5-(chlorosulfony1)-1-methy1-1H-pyrrole-2-carboxylate to obtain the title compound. 1HNMR (300 MHz, CDC13): 6 7.37 (dd, J= 1.8 & 10.5 Hz, 1H), 7.29 (m, 2H), 7.12-6.94 (m, 4H), 5.87 (dt, J= 1.8, 8.4 & 17.4 Hz, 1H), 5.56 (br s, 1H), 3.65 (s, 3H), 3.75 (s, 3H).
Example 39 N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)pheny1)-5-methylisoxazole-4-sulfonamide:
II NH H F
SFOI
According to the general procedure A, 5,6-difluoro-N1-(2-fluoro-4-iodophenyl)benzene1,2-diamine was reacted with the corresponding sulfonyl chloride to obtain the title compound.
Yield: 22%. m/z = 508 [MAI.
Example 40 3-Chloro-N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)phenyl)propane-1-sulfonamide:
CI
0 i\11-1 H F
According to the general procedure A, 5,6-difluoro-N1-(2-fluoro-4-iodophenyl)benzene-1,2-diamine was reacted with 3-chloropropane-1-sulfonyl chloride to obtain the desired product. 114 NMR (500 MHz, CDC13): 8 = 7.39-7.38 (d, 1H), 7.35-7.34 (m, 1H), 7.27-7.26 (m, 1H), 7.10-7.0 (q, 1H), 6.63 (s, 1H, br), 6.15-6.11 (q, 1H), 5.60 (s, 1H, br), 3.60-3.56 (t, 2H), 3.22-3.20 (m, 2H), 2.22-2.16 (m, 2H).
General procedure C: Synthesis of N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)pheny1)-2-(alkylamino)ethanesulfonamide:
2-Chloro-ethanesulfonyl chloride (0.1 ml, 1 mmol) was added to a solution of 5,6-difluoro-N1-(2-fluoro-4-iodophenyObenzene-1,2-diamine (0.364 g, 1 mmol) and triethylamine (0.28 ml, 2 mmol) in CH2Cl2 (5 ml) and the reaction mixture was stirred at room temperature for 16h. Then it's treated with an excess amine (10 eq) either in solution or as a neat liquid. The reaction mixture stirred at room temperature for additional 6h. The reaction mixture diluted with CH2C12 (10 ml) and water (10 m1). The organic layer was sequentially washed with dil.
HC1(2x20 ml, 2N) and saturated NaHCO3 (2x10 ml) solution. Then the CH2C12 layer dried (MgSO4) and evaporated to obtain the crude product. The impure product was purified under preparative HPLC conditions to obtain the pure products in 50-60 % yield.
Example 41 N-(2-(4-chloro-2-fluorophenylamino)-3,4-difluorophenyl) cyclopropanesulfonamide:
0'NH
N
CI
See example 1. 1H NMR (300 MHz, CDC13) 60.85-0.95 (m, 2H), 1.05-1.15 (m, 2H), 2.2-2.4 (m, 1H), 5.8 (s, 1H), 6.3 (t, 1H), 6.6-7.4 (m, 5H); m/z = 375 [M-lf.
Example 42 N-(3,4-difluoro-2-(4-iodo-2-methylphenylamino)phenyl)cyclopropanesulfonamide:
oy See example 1. IH NMR (CDC13) 60.80-1.0 (m, 211), 1.05-1.20 (m, 211), 1.55 (s, 311), 2.4-2.5 (m, 1H), 5.6 (s, 1H), 6.2 (dd, 1H), 6.4 (s, 111), 7.1 (q, 1H). 7.3-7.4 (m, 211), 7.5 (s, 1H); m/z = 463 {m-if.
Example 43 N-(2-(4-tert-butyl-2-chlorophenylamino)-3,4-difluorophenyl) cyclopropanesulfonamide:
oy See example 1. 1}INMR (300 MHz, CDC13) 60.9-1.0 (m, 211), 1.05-1.20 (m, 2H), 1.3 (s, 9H), 2.4-2.5 (m, 1H), 5.8 (s, 1H), 6.3 (dd, 1H), 6.6 (s, 111), 7.0-7.2 (m, 2H), 7.3-7.4 (m, 211); m/z= 413 [M-l].
Example 44 N-(2-(2,4-dichlorophenylamino)-3,4-difluorophenyl)cyclopropanesulfonamide:
oy CI
See example 1. 111NMR (300 MHz, CDCI3) 8 0.9-1.0 (m, 2H), 1.05-1.20 (m, 2H), 2.4-2.5 (m, 1H), 6.0 (s, 1H), 6.3 (dd, 111), 6.6 (s, 1H), 7.0-7.2 (m, 2H), 7.3-7.4 (m, 2H); m/z =
392 [M-lf.
Example 45 3-Chloro-N-(3,4-difluoro-2-(2-fluoro-4-trifluoromethyl) phenylamino)phenyl)propane-1-sulfonamide:
H NH H F
See example 1.1H NMR (300 MHz, CDC13): 67.39-7.26 (m, 2H), 7.25 (m, 1H), 7.18 (dd, J= 9.0 & 17.7 Hz, 1H), 6.78 (br s, D20 exchangeable, 1H), 6.50 (t, J= 8.1 Hz, 1H), 6.00 (br d, D20 exchangeable, J= 1.5 Hz, 1H), 3.63 (t, J= 6.0 & 6.3 Hz, 211), 3.29 (t, J= 7.2 &
7.8 Hz, 2H), 2.26 (quintet, 2H); m/z = 445 [M-lf.
Example 46 N-(3,4-difluoro-2-(2-chloro-4-trifluoromethyl)phenylamino)methanesulfonamide:
s, NH H CI
N
See example 1.1H NMR (300 MHz, CDC13): 8 7.65 (d, J=7.8 Hz, 111), 7.33 (m, 211), 7.19 (dd, J= 9.3 & 17.4 Hz, 111), 6.90 (br s, D20 exchangeable, 1H), 6.45 (dd, J=1.5 & 8.4 Hz, 111), 6.39 (br s, D20 exchangeable, 1H), 3.02 (s, 3H); in/z = 399 [M-lf.
Example 47 3-Chloro-N-(3,4-difluoro-2-(2-chloro-4-trifluorom ethyl) phenylamino)phenyl)propane-1-sulfonamide:
H CI
N
See example 1.1H NMR (300 MHz, CDCI3): 5 7.66 (d, J= 1.5 Hz, 1H), 7.36 (m, 2H), 7.19 (dd, J= 9.0 & 17.4 Hz, 1H), 6.91 (br s, D20 exchangeable, 11-1), 6.50 (dd, J= 8.4 & 1.5 Hz, 1H), 6.37 (s, D20 exchangeable, 1H), 3.62 (t, J= 6.0 Hz, 2H), 3.29 (t, J=7.5 & 7.8 Hz, 2H), 2.27 (quintet, 2H); in/z = 462 [M-lf.
Example 48 3-Chloro-N-(3,4-difluoro-2-(2-bromo-4-trifluoromethyl) phenylamino)phenyl)propane-1-sulfonamide:
rt NH H Br N
See example 1.1H NMR (300 MHz, CDCI3): 8 7.82 (s, 1H), 7.38 (m, 2H), 7.20 (dd, J
= 9.0 & 17.7 Hz, 1H), 6.62 (br s, D20 exchangeable, 1H), 6.43 (d, J= 8.4 Hz, 1H), 6.23 (s, D20 exchangeable, 1H), 3.65 (t, J= 6.0 Hz, 2H), 3.30 (t, J= 7.5 Hz, 2H), 2.28 (quintet, 2H);
m/z = 506 [M-1T.
Example 49 Cyclopropanesulfonic acid (3,4,6-trifluoro-2-(2-fluoro-4-iodo-phenylamino)-phenyl)-amide:
Step A (2-Fluoro-4-iodo-phenyl)-(2,3,5-trifluoro-6-nitro-phenyp-amine:
F I
F
A stirred solution of 2-fluoro-4-iodoaniline (3.64 gm, 15.37 mmol) in dry THE' (100 ml) under nitrogen was cooled to -78 C and a solution of 1.0 M lithium hexa methyl disilazide (LiN(SiMe3)2) "LHMDS" (15.37 ml, 15.37 mmol) was added slowly. This reaction mixture was kept stirring at -78 C for another hour and then 2,3,4,6-tetrafluoronitrobenzene was added. The reaction mixture was allowed to warm to room temperature and stirring continued for another 16 hours. Ethyl acetate (200 ml) was added to the reaction mixture and was washed with water. Organic layer was dried over sodium sulfate and further purified by column chromatography to provide yellow solid (3.75 gm, yield: 59.24%). M-H+:
410.9.111 NMR (DMSO, 300 MHz): 6.85 (t, 1H); 7.38 (d, 1H); 7.62 (m, 2H); 8.78 (s, 1H).
Step B 3,4,6-Trifluoro-N2-(2-Fluoro-4-iodo-phenyl)-benzene-1,2-diamine:
F I
F
To the stirred solution of (2-fluoro-4-iodo-pheny1)-(2,3,5-trifluoro-6-nitro-pheny1)-amine 3 (5.2 gm, 12.62 mmol) in Et0H (200 ml), ammonium chloride (10.12 gm, 189.3 mmol) and iron powder (10.57 gm, 189.3 mmol) was added. This reaction mixture was kept stirring at reflux for 16 hours. Reaction mixture was allowed to cool and was filtered over celite and concentrated to dryness. The residue obtained was taken into Et0Ac and was washed with water. The Et0Ac layer was dried over sodium sulfate and further purified by crystallization from Et0H to provide off-white solid (3.2 gm, yield: 66.39%).
M-H+: 381.1.
1H NMR (DMSO, 300 MHz): 5.0 (s, 2H); 6.2 (t, 1H); 7,2 - 7.3 (m, 2H); 7.45 (s, 1H); 7.5 (d, 1H).
Step C: 4,6,7-Trifluoro-1-(2-Fluoro-4-iodo-pheny1)-1,3,-dihydrobenzoimidazole-one:
H, P
N--`( F N
To the stirred solution of 3,4,6-trifluoro-N2-(2-Fluoro-4-iodo-pheny1)-benzene-1,2-diamine 3 (0.285 gm, 0.74 mmol) in CH2C12 (2 ml), 1,1'-carbonyldiimidazole (0.125 gm, 0.75 mmol) was added. This reaction mixture was kept stirring at room temperature for 16 hours when product precipitated out. The white solid was filtered and used further without any purification. (0.2 gm, yield: 65.85%); m/z = 407 [M-1]-.
Step DIE: Cyclopropanesulfonic acid (3,4,6-trifluoro-2-(2-fluoro-4-iodo-phenylamino)-pheny1)-amide:
0õ
F lel N 1110 A stirred solution of 4,6,7-trifluoro-1-(2-fluoro-4-iodo-pheny1)-1,3,-dihydrobenzimidazol-2-one (0.2 gm, 0.41 mmol) in dry THF (4 ml) under nitrogen was cooled to -78 C and a solution of 1.0 M LiHMDS (0.41 ml, 0.41 mmol) was added slowly. (2 ml) followed by addition of cyclopropanesulfonyl chloride (0.050 ml, 0.49 mmol). This reaction mixture was kept stirring at room temperature for 16 hours, concentrated to dryness and was taken into Et0Ac. The Et0Ac was washed with water, dried over sodium sulfate and concentrated to dryness. The residue obtained 1-cyclopropanesulfony1-4,5,7-trifluoro-3-(2-fluoro-4-iodo-pheny1)-1,3-dihydro-benzimidazol-2-one 5 was taken into dioxane (2 ml) and to this 1.0 N NaOH (0.5m1) was added and kept stirring at room 50 C for 16 hours. TLC
indicated incomplete reaction, the product was purified by HPLC to provide off-white solid (4.4 mg) M+H+: 484.7, M-le: 486.7.1H NMR (CDC13, 300 MHz): 0.9 ¨ 1.1 (m, 2H);
1.1 -1.2 (in, 2H); 2.45 ¨2.55 (m, 1H); 6.05 (s, 1H); 6.44 ¨ 6.54 (m, 1 H); 7.1 (s, 1H); 7.4 ¨ 7.7 (d, 1H); 7.38 ¨ 7.44 (dd, 1H); ni/z = 485 [M-lf.
Example 50 N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)-6-ethoxyphenyl)cyclopropane sulfonamide:
Step A: (2,3-Difluoro-5-methoxy-6-nitro-pheny1)-(2-fluoro-4-iodo-pheny1)-amine:
Me N
A stirred solution of (2-fluoro-4-iodo-phenyl)-(2,3,5-trifluoro-6-nitro-pheny1)-amine (1.23 gm, 3 mmol) in dry THF (25 ml) under nitrogen was cooled to -78 C and a solution of 25% Na0Me (0.68 ml, 0.3 mmol) was added slowly. Reaction mixture was allowed to warm to room temperature and stirring continued for another 16 hours. TLC indicated incomplete reaction. Ethyl acetate (100 ml) was added to the reaction mixture and was washed with water. Organic layer was dried over sodium sulfate and further purified by column chromatography to provide yellow solid (0.6 gm, yield: 47.6%). m/z = 424 [M=H1-Step B: 5,6-Difluoro-N1-(2-fluoro-4-iodopheny1)-3-methoxybenzene-1,2-diamine:
Me0 N
To the stirred solution of (2,3-difluoro-5-methoxy-6-nitro-phenyl)-(2-fluoro-4-iodo-phenyl)-amine (0.57 gm, 1.34 mmol) in Et0H (20 ml), ammonium chloride (1.18 gm, 20.16 mmol) and iron powder (1.15 gm, 21.44 mmol) was added. This reaction mixture was kept stirring at reflux for 16 hours. Reaction mixture was allowed to cool and was filtered over celite and concentrated to dryness. The residue obtained was taken into Et0Ac and was washed with water. The Et0Ac layer was dried over sodium sulfate and further purified by crystallization from Et0H to provide off-white solid (0.47 gm, yield: 90.3%).
M-H+: 393.2.
1H NMR (DMSO, 300 MHz): 3.76 (s, 3H); 6.1 (t, 1H); 6.8 - 7.0 (m, 1H); 7.2 (d, 1H); 7.35 (s, 1H); 7.42 (d, 1H).
Step C: 6,7-Difluoro-1-(2-fluoro-4-iodopheny1)-4-methoxy-1H-benzo[d]imidazol-2(3H)-one:
H p Me0 N
To the stirred solution of 5,6-difluoro-N1-(2-fluoro-4-iodopheny1)-3-methoxybenzene-1,2-diamine (0.17 gm, 0.43 mmol) in CH2Cl2 (2 ml), 1,1'-Carbonyldiimidazole (0.085 gm, 0.53 mmol) was added. This reaction mixture was kept stirring at room temperature for 16 hours when product precipitated out. The white solid was filtered and used further without any purification. (0.089 gm); m/z = 419 [M-1].
Step fl/F: N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)-6-methoxyphenyl) cyclopropanesulfonamide:
,0 H
Me0 N
A stirred solution of 1-(cyclopropylsulfony1)-4,5-difluoro-3-(2-fluoro-4-iodopheny1)-7-methoxy-1H-benzo[djimidazol-2(3H)-one (0.89 gm, 0.17 mmol) in dry THF (4 ml) under nitrogen was cooled to -78 C and a solution of 1.0 M LiHMDS (0.17 ml, 0.17 mmol) was added slowly. (2 ml) followed by addition of Cyclopropanesulfonyl chloride (0.021 ml, 0.21 mmol). This reaction mixture was kept stirring at room temperature for 16 hours, concentrated to dryness and was taken into Et0Ac. The Et0Ac was washed with water, dried over sodium sulfate and concentrated to dryness. The resulting 1-(cyclopropylsulfony1)-4,5-difluoro-3-(2-fluoro-4-iodopheny1)-7-methoxy-1H-benzo[d]imidazol-2(3H)-one was taken into dioxane (2 ml) and to this 1.0 N NaOH (0.5m1) was added and kept stirring at room 50 C
for 16 hours. TLC indicated incomplete reaction, the product was purified by HPLC to provide off-white solid (2.5 mg) M+H+: 484.7, M-H+: 497.3. 11-1 NMR (CDC13, 300 MHz):
0.85 ¨0.95 (m, 2H); 1.05 ¨1.15 (m, 2H); 2.4 ¨ 2.5 (m, 1H); 3.9 (s, 3H); 6.1 (s, 1H); 6.4 ¨ 6.6 (m, 2 H); 7.3 (m, 1H); 7.35 ¨ 7.4 (dd, 111); m/z = 497 [-m-if.
Example 51 Methylsulfonic acid (3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-6-methoxy-pheny1)-amide:
$0 I
0sNH
Me0 N
A stirred solution of 5,6-difluoro-N1-(4-fluoro-2-iodopheny1)-3-methoxybenzene-1,2-diamine (0.150 gm, 0.38 mmol) in dry CH2C12 (4 ml), TEA (.264 ml, 1.9 mmol) and Methanesulfonyl chloride was added slowly. This reaction mixture was kept stirring at room temperature for 16 hours, TLC indicated incomplete reaction along with starting material two products were observed. The reaction mixture was washed with water, organic layer was dried over sodium sulfate and concentrated to dryness. the product was purified by column chromatography. The minor product was found to be the expected compound (6.4 mg). M-H+: 471.5. 1H NMR (CDC13, 300 MHz): 3.9 (s, 3H); 6.05 (s, 1H); 6.4 ¨ 6.5 (m, 11-1'); 6.5 ¨6.6 (m, 1H); 7.2 (s, 1H); 7.28 (d, 1H); 7.35 ¨ 7.4 (d, 1H); m/z = 471 pvi-ir.
Example 52 1-(2,3-Dihydroxy-propyI)-cyclopropanesulfonic acid [3,4,6-trifluoro-2-(2-fluoro-4-iodo-phenylamino)-phenyll-amide:
Step A: 1-Allyl-cyclopropanesulfonic acid [3,4,6-trifluoro-2-(2-fluoro-4-iodo-phenylamino)-phenyl]-amide:
II 'NH H F
5 According to the general procedure B, 1-allyl-cyclopropanesulfonyl chloride was reacted with 3,5,6-trifluoro-N1-(2-fluoro-4-iodophenyl)benzene-1,2-diamine to obtain the title product. 114 NMR (CDC13, 300 MHz): 5 7.41 (dd, 1H), 7.38 (dd, 1H), 7.09 (s, 1H), 6.78 (m, 1H), 6.49 (m, 1H), 5.96 (s, 1H), 5.86 (m, 1H), 5.18 (d, 2H), 2.76 (d, 2H), 1.23 (m, 2H), 0.872 (m, 2H).
Step B: 1-(2,3-Dihydroxypropy1)-N-(3,4,6-trifluoro-2-(2-fluoro-4-iodophenylamino) phenyl)cyclopropane-l-sulfonamide:
HO
n'NH H F
1-Allyl-cyclopropanesulfonic acid [3,4,6-trifluoro-2-(2-fluoro-4-iodo-phenyl amino)-phenyl]-amide ( 110 mg, 0.21 mmole) and 4-methylmorpholine N-oxide (24.6 mg, 0.21 mmole) was dissolved in TIE (8 mL). Osmium tetroxide was added at room temperature (0.021 mmole, 0.153 mL, 4% in H20) and the reaction mixture was stirred at room temperature for 16 hours. Et0Ac was added, the organic phase was washed with water, dried (MgSO4) and concentrated under reduced pressure. The residue was purified over silica gel chromatography (eluants: Et0Ac/ Me0H) to obtain the titled product (0. 89 g, 75 %). 1H
NMR (CDC13, 300 MHz): 5 7.39 (dd, J = 1.5 & 10.6 Hz, 1H), 7.29 (d, J = 8.8 Hz, 1H), 7.28 (s, 1H), 6.97 (s, 1H), 6.76 (m, 1H), 6.49 (m, 111), 4.13 (m, 1H), 3.66 (dd, J
= 3.7 & 11.4 Hz, 1H), 3.53 (dd. J = 6.7 & 112 Hz, 1H), 2.50(dd, J = 10,0 & 16.1 Hz, 1H), 1.6 (m,1H), 1.46 (m, 1H), 1.28 (m, 1H), 1.20 (m, 2H), 0.92 (m, 2H); in/z = 559 Example 53 (S)-1-(2,3-dihydroxypropy1)-N-(3,4,6-trifluoro-2-(2-fluoro-4-iodophenylamino) phenyl)cyclopropane-1-sulfonamide:
NH HO
H F
The pure S isomer was obtained by chiral HPLC separation of the racemic mixture (example 52). 1H NMR (CDC13, 300 MHz): 8 7.39 (dd, J = 1.5 & 10.6 Hz, 111), 7.29 (d, J =-8.8 Hz, 1H), 7.28 (s, 1H), 6.97 (s, 1H), 6.76 (m, 1H), 6.49 (m, 1H), 4.13 (m, 1H), 3.66 (dd, J
= 3.7 & 11.4 Hz, 1H), 3.53 (dd. J'= 6.7 & 11.2 Hz, 1H), 2.50(dd, J= 10.0 &
16.1 Hz, 1H), 1.6 (m,1H), 1.46 (m, 1H), 1.28 (m, 1H), 1.20 (m, 2H), 0.92 (m, 2H); m/z = 559 [M-ir.
Example 54 (R)-1-(2,3-dihydroxypropy1)-N-(3,4,6-trifluoro-2-(2-fluoro-4-iodophenylamino) phenypcyclopropane-1-sulfonamide:
Ho,F,A1 Tr NH H F
The pure R isomer was obtained by chiral HPLC separation of the racemic mixture (example 52).1H NMR (CDC13, 300 MHz): 5 7.39 (dd, J = 1.5 & 10.6 Hz, 11-1), 7.29 (d, J =
8.8 Hz, 1H), 7.28 (s, 1H), 6.97 (s, 111), 6.76 (m, 1H), 6.49 (m, 1H), 4.13 (m, 1H), 3.66 (dd, J
= 3.7& 11.4 Hz, 1H),3.53 (dd. J = 6.7 & 11.2 Hz, 1H), 2.50(dd, J = 10.0& 16.1 Hz, IH), 1.6 (m,1H), 1.46 (m, 1H), 1.28 (m, 111), 1.20 (m, 2H), 0.92 (m, 211); tn/z =
559 [M-11".
Example 55 N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)-6-methoxypheny1)-1-(2,3-dihydroxypropypeyclopropane-1-sulfonamide:
Step A: 1-Allyl-N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)-6-methoxyphenyOcyclopropane-l-sulfonamide p NH H F
I
Me0 According to the general procedure B, 1-allyl-cyclopropanesulfonyl chloride was reacted with 5,6-difluoro-N1-(2-fluoro-4-iodopheny1)-3-methoxybenzene-1,2-diamine to obtain the title product. 1HNMR (CDC13, 300 MHz): 8 7.417 (dd, 1H), 7.309(s, 111), 7.25 (m, 111), 6.89 (m, 111), 6.52(m, 1H), 6.427 (m, 111), 6.03 (s,1H), 5.668 (m, 111), 5.11 (t, 1H), 3.9 (s, 3H), 2.75 (d, 2H), 1.21 (m, 2H), 0.767 (m, 211).
Step B: N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)-6-methoxypheny1)-1-(2,3-dihydroxypropyl)cyclopropane-1-sulfonamide HO
NH H F
Me0 la 1-Allyl-N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)-6-methoxyphenyl) cyclopropane-1 -sulfonamide ( 97 mg, 0.18 mmole) and 4-methylmorpholine N-oxide (21 mg, 0.18 mmole) were dissolved in TIM (8 mL). Osmium tetroxide was added at room temperature (0.018 mmole, 0.13 mL, 4% in H20) and the reaction mixture was stirred at room temperature for 16 hours. Et0Ac was added, the organic phase was washed with water, dried (MgSO4) and concentrated under reduced pressure. The residue was purified over silica gel chromatography (eluants: Et0Ac/ Me0H) to obtain the titled product (0. 80 g, 78 %). 1H
NMR (CDC13, 300 MHz): 5 7.38 (dd, J = 1.7 & 10.3 Hz,1H), 7.26 (m, 1H), 7.14 (s, 1H), 6.87 (s, 1H), 6.53 (dd, J = 6.8 & 11.4 Hz, 1H), 6.43 (m, 1H), 4.06 (m, 1H), 3.89 (s, 3H), 3.63 (dd, J = 3.7 & 11.1 Hz, 1H), 3.49 (dd, J = 6.4 & 11.1 Hz, 1H), 2.3 (dd, J =
9.7 & 16.1 Hz, 1H), 1.77 (dd, J = 1.9 & 16.0 Hz, 1H), 1.37 (m, 1H), 1.25 (m, 111), 1.21 (m, 2H), 0.86 (m, 2H); m/z = 571 [M-1]..
Example 56 (S)-N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)-6-methovpheny1)-1-(2,3-dihydroxypropyl)cyclopropane-l-sulfonamide:
5;5) HO
NH H F
Me0 The pure S isomer was obtained by chiral HPLC separation of the racemic mixture (example 55).1H NMR (CDC13, 300 MHz): 5 7.38 (dd, J = 1.7 & 10.3 Hz,1H), 7.26 (m, 111), 7.14 (s, 1H), 6.87 (s, 1H), 6.53 (dd, J = 6.8 & 11.4 Hz, 1H), 6.43 (m, 1H), 4.06 (m, 1H), 3.89 (s, 3H), 3.63 (dd, J = 3.7 & 11.1 Hz, 1H), 3.49 (dd, 3= 6.4 & 11.1 Hz, 1H), 2.3 (dd, J = 9.7 &
16.1 Hz, 1H), 1.77 (dd, J = 1.9 & 16.0 Hz, 1H), 1.37 (m, 1H), 1.25 (m, 1H), 1.21 (m, 2H), 0.86 (m, 2H); m/z = 571 [M-lf.
Example 57 (R)-N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)-6-methoxypheny1)-1-(2,3-dihydroxypropyl)cyclopropane-1-sulfonamide:
µ--7H 0 ri NH H F
Me0 The pure R isomer was obtained by chiral HPLC separation of the racemic mixture (example 55). HN1vIR (CDC13, 300 MHz): 8 7.38 (dd, J = 1.7 & 10.3 Hz,1H), 7.26 (m, 1H), 7.14 (s, 1H), 6.87 (s, 1H), 6.53 (dd, J = 6.8 & 11.4 Hz, 1H), 6.43 (m, 1H), 4.06 (m, 1H), 3.89 (s, 3H), 3.63 (dd, J = 3.7 & 11.1 Hz, 111), 3.49 (dd, J = 6.4 & 11.1 Hz, 1H), 2.3 (dd, J = 9.7 &
16.1 Hz, 1H), 1.77 (dd, J = 1.9 & 16.0 Hz, 1H), 1.37 (m, 1H), 1.25 (m, 1H), 1.21 (m, 2H), 0.86 (m, 2H); nilz = 571 {m-if.
Example 58 1-(2-hydroxyethyl)-N-(3,4,6-trifluoro-2-(2-fluoro-4-iodophenylamino)phenyl) cyclopropane-1-sulfonamide:
Step A: TBS-protected 1-(2-hydroxyethyl)-N-(3,4,6-trifluoro-2-(2-f1uoro-4-iodophenylamino)phenyl) cyclopropane-1-sulfonamide:
OTBS
Ataqe0 According to the general procedure B, the sulfonyl chloride prepared in step C
of example 16 was reacted with 5,6-difluoro-N1-(2-fluoro-4-iodopheny1)-3-fluorobenzene-1,2-diamine to obtain the title product. Yield: 13%. 1H-NMR (300 MHz, CDC13): 6 =
7.51 (s, 1H, br), 7.37-7.35 (d, 1H), 7.27-7.25 (d, 1H), 6.94 (s, 1H, br), 6.78-6.68 (m, 1H), 6.46-6.44 (m, 111), 3.90-3.88 (t, 211), 2.12-2.10 (t, 2H), 1.31-1.28 (m, 211), 0.91-0.89 (m, 2H), 0.86 (s, 9H), 0.05 (s, 6H); m/z = 643 [M-lf.
Step B: 1-(2-hydroxyethyl)-N-(3,4,6-trifluoro-2-(2-fluoro-4-iodophenylamino)-phenyl) cyclopropane-l-sulfonamide:
(OH
Ao o' NH H F
FoN0 Same procedure as in step E, example 16. Yield: 100%. 1H-NMR (300 MHz, CDC13):
5 = 7.51 (s, 1H, br), 7.37-7.35 (d, 1H), 7.27-7.25 (d, 1H), 6.94 (s, 1H, br), 6.78-6.68 (m, 1H), 6.46-6.44 (m, 1H), 3.90-3.88 (t, 2H), 2.12-2.10 (t, 2H), 1.31-1.28 (m, 2H), 0.91-0.89 (m, 211);
nz/z = 529 [M-1T.
Example 59 N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)-6-methoxyphenyI)-1-(2-hydroxyethyl)cyclopropane-1-sulfonamide:
Step A: TBS-protected N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)-6-methoxypheny1)-1-(2-hydroxyethyl)cyclopropane-1-sulfonamide:
(OTBS
,0 NH H F
N
According to the general procedure B, the sulfonyl chloride prepared in step C
of example 16 was reacted with 5,6-difluoro-N1-(2-fluoro-4-iodopheny1)-3-methoxy-benzene-1,2-diamine to obtain the title product. Yield: 37%. 111-NM:ft (300 MHz, CDC13): 5 = 7.40-7.34 (dd, 1H), 7.23-7.21 (m, 1H), 6.61 (s, 1H, br), 6.57-6.49 (dd, 1H), 6.48-6.39 (m, 1H), 3.9-3.7 (m, 5H), 2.15-2.05 (t, 2H), 1.30-1.20 (m, 2H), 0.95-0.80 (m, 1114), 0.05 (s, 6H); m/z =
655 EM-if.
Step B: N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)-6-methoxypheny1)-1-(2-hydroxyethyl)cyclopropane-1-sulfonamide:
(OH
AlAlk, 0 lel la Same procedure as in step E, example 16. Yield: 100%. 1H-NMR (300 MHz, CDC13):
= 7.40-7.34 (dd, 1H), 7.23-7.21 (m, 1H), 6.61 (s, 1H, br), 6.57-6.49 (dd, 1H), 6.48-6.39 (m, 1H), 3.9-3.7 (m, 511), 2.15-2.05 (t, 2H), 1.30-1.20 (m, 2H), 0.95-0.80 (m, 2H); m/z = 541 [M-11".
Example 60 N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)-6-methoxypheny1)-1-(3-hydroxy-2-(hydroxymethyl)propyl)cyclopropane-l-sulfonamide:
Step A: Dimethyl 2-(2-bromoallyl)malonate:
Me0).)-LOMe Br To a suspension of sodium hydride (5.0 g, 125 mmol) in HMPA (50 ml, distilled from calcium hydride) was added a solution of dimethyl malonate (11.7 ml, 100 mmol) in HMPA
(5 ml) at 0 C under argon. The mixture was heated to 50 C and stirred 1 hour.
Following this the solution was again cooled to 0 C, and a solution of 2,3-dibromopropene (12.2 ml, 100 mmol) in HMPA (5 ml) was added to the reaction mixture. Next, the solution was warmed to 40 C and stirred for 1 hour. The reaction mixture was quenched with aq. HC1 (10%, 88 ml) and extracted with ether (3 x 45 m1). The organic fractions were collected, dried over MgS0-4, and the solvent was removed in vacuo . The crude oil was purified via silica gel chromatography (eluants: chloroform/hexane) to obtain the titled product as a colorless oil (16.3 g, 65%). H-NMR (300 MHz, CDC13) 6 5.70 (d, J = 1.8 Hz, 1 H), 5.48 (d, J
= 1.8 Hz, 1H), 3.63 (t, J = 7.5 Hz, 1 H), 3.76 (s, 6 H), 3.04 (d, J = 7.5 Hz, 2 H).
Step B: 2-(2-Bromoallyl)propane-1,3-diol:
OH OH
is Br Lithium aluminum hydride (1.9 g, 7.65 mmol) was slurried in anhydrous diethyl ether (50 ml) and cooled to -78 C in a dry ice/acetone bath. A solution of the product from step A
(0.639 g, 16.84 mmol) in dry ether (26 ml) was then added dropwise. After the malonate was added, the solution was allowed warm to room temperature and stirring was continued for 3 hours. The reaction was quenched with brine (50 ml), extracted with ethyl acetate (3 x 25 ml) and dried over MgSO4. The solvent was removed in vacuo to give the desired product (1.3 g, 86%) which was used for the next step without further purification. 1H-NMR (300 MHz, CDC13) 65.66 (d, J= 1.2 Hz, 1 H), 5.48 (d, J = 1.5 Hz, 1H), 3.86 (m, 2 H), 3.73 (m, 2 H), 2.51 (d, J = 7.5 Hz, 2 H), 2.40 (br s, 2 H), 2.15 (m, 1 H).
Step C: Di-tert-butyldimethylsilyl protected 2-(2-bromoallyl)propane-1,3-diol:
TBSO¨\ )¨Br TBSO--/
The product from step B (2.8 g, 14.20 mmol) was dissolved in anhydrous THF
(140 m1). Anhydrous pyridine (2.5 ml, 31.24 mmol) was added, and the solution was cooled to 0 C. tert-Butyldimethylsilyltriflate (7.2 ml, 31.24 mmol) was added dropwise, and upon completion, the reaction solution was heated to 35 C. After stirring for 6 days, the reaction was quenched with 100 ml brine, extracted with ethyl acetate (3 x 50 ml) and dried over MgSO4. The combined organic phases were evaporated to obtain the crude product (5.5 g, 91%) as a yellow oil which was used in the next step without further purification. 1H-NMR
(300 MHz, CDC13) 8 5.54 (d, J = 0.9 Hz, 1 H), 5.40 (d, J = 1.2 Hz, 1H), 3.55 (d, J = 5.4, 4 H), 2.40 (d, J = 6.9 Hz, 2 H), 1.97 (m, 1 H), 0.85 (s, 18 H), 0.02 (s, 911).
Step D: Di-tert-butyldimethylsilyl protected 24(1-bromocyclopropyl)methyl) propane-1,3-diol:
TBSO-\
A reaction flask was charged with anhydrous CH2C12 (10 ml) and diethyl zinc (1.0 M
in hexanes, 4.65 ml, 4.65 mmol) at 0 C. Trifluoroacetic acid (0.358 ml, 4.65 mmol) was added dropwise and the solution was allowed to stir for 20 minutes.
Diiodomethane (0.375 ml, 4.65 mmol) was then added and the solution was stirred for another 20 minutes. Finally, the product from step C (0.492 g, 1.16 mmol) was added and the solution was allowed to warm to ambient temperature, stirring for 16 hours. The reaction was quenched with saturated aqueous NH4C1. The layers were partitioned and the aqueous phase was extracted with chloroform (3 x 5 m1). The combined organic phases were washed with brine (10 ml), dried over MgSO4, and the volatiles were removed in vacuo. The resulting crude was purified via silica gel chromatography (eluants: chloroform/hexanes) to provide the product as a clear oil (0.280 g, 64%). 1H-NMR (300 MHz, CDC13) 6 3.66 (d, J = 5.4, 4 H), 2.08 (m, 1 H), 1.64 (d, J = 6.9, 211), 1.13 (m, 2 H), 0.88 (s, 18 H), 0.81 (m, 2 H), 0.04 (s, 911).
Step E: Di-tert-butyldimethylsilyl protected 1-(3-hydroxy-2-(hydroxymethyl)propyl) cyclopropane-l-sulfonyl chloride:
TBSO--\
it __________________________________________ 0 The product from step D (0.507 g, 1.16 mmol) was dissolved in anhydrous ether (6 ml) and the reaction solution was cooled to -78 C. Following this, tert-butyllithium (1.7 M in pentane, 1.50 ml, 2.55 mmol) was added dropwise over 5 minutes. After stirring for 0.5 hours, the lithiated product was transferred via cannula to a stirred solution of sulfuryl chloride (0.206 ml, 2.55 mmol) in dry ether (6 ml) at -78 C. Once the transfer is complete, the solution was allowed to warm to room temperature, the solvent was evaporated and the resulting white solid was slurried in dry hexanes. This slurry was immediately filtered through celite, and all volatiles were removed in vacuo. The resulting crude product (0.376 g, 71%) was isolated as a yellow oil and was used in the following step without further purification. 1H-NMR (300 MHz, CDC13) 8 3.60 (m, 4 H), 2.16 (m, 1 H), 2.03 (d, 2 H), 0.88 (s, 18 H), 0.04 (s, 9 H).
Step F: Di-tert-butyldimethylsilylprotected N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)-6-methoxypheny1)-1-(3-hydroxy-2-(hydroxymethyl)propyl) cyclopropane-1-sulfonamide:
TBS\O 0,TBS
4Y,0 01 'NH
N
5,6-difluoro-N1-(2-fluoro-4-iodopheny1)-3-methoxybenzene-1,2-diamine (8.8 mg, 0.022 mmol) was dissolved in anhydrous pyridine (0.5 ml) under an argon atmosphere. The product from step E (20.5 mg, 0.045 mmol), dissolved in dry pyridine (0.5 ml), was added to the reaction flask and the mixture was heated at 80 C for 21 hours. The solvent was removed in vacuo and the resulting crude was purified via silica gel chromatography (eluents: ethyl acetate/hexanes) to provide the title compound (2.75 mg, 15%). m/z 813.5 (M-1).
Step G: N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)-6-methoxypheny1)-1-(3-hydroxy-2-(hydroxymethyl)propyl)cyclopropane-1-sulfonamide:
OH OH
,K
0/ 'NH F
H
F I
F
The product from step F (27.9 mg, 0.0342 mmol) was dissolved in THF (1 ml) and treated with aqueous HC1 (1.2 N, 0.2 ml) at 0 C. The resulting solution was stirred for 4 hours. Following this, the reaction was quenched with saturated aqueous NaHCO3, extracted with ethyl acetate, dried over MgSO4 and the volatiles were removed in vacuo.
The resulting crude was purified via silica gel chromatography (eluents:
methanol/chloroform) followed by LC-MS purification to provide the title compound (11.8 mg, 59%). 11-1-NMR (300 MHz, CD30D) 8 7.32 (dd, 1 H), 7.21 (d, 1 H), 6.76 (dd, 1 H), 6.33 (m, 1 H), 3.82 (s, 3 H), 3.52 (d, 4 H), 2.01 (m, 1 H), 1.88 (d, 2 H), 1.07 (m, 2 H), 0.75 (m, 2 H), m/z 585.3 (M-1).
Example 61 N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)-6-methoxyphenyl) cyclobutane sulfonamide:
Step A: Cyclobutanesulfonyl chloride:
q so,ci To a suspension of Mg turnings (0.790 g, 32.5 mmol) in 20 ml anhydrous diethyl ether was added a solution of cyclobutylbromide (1.8 ml, 2.5722 g, 19.1 mmol) in 20 ml diethyl ether in small portions with strong stirring. After the initial exothermic reaction had ceased, the mixture was further heated to the reflux temperature for 30 min.
The suspension was cooled down to room temperature and the supernatant was added in small portions to an ice-cold solution of sulfuryl chloride (4.6 ml, 7.728 g, 57.2 mmol) in 30 ml anhydrous DCM.
After complete addition, the suspension was warmed to room temperature and the volatiles were removed in vacuo. The residue was dried in oil-pump vacuo for 15 min, then it was extracted with hexane (150 m1). The hexane suspension was filtered and the hexane was removed in vacuo to give the crude product as dark purple oil which was used for the next step without further purification. There is still some unreacted cyclopropylbromide present.
Crude yield: 1.1 g (38%).
Step B: N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)-6-methoxyphenyl) cyclobutanesulfonamide Me0 N
According to the general procedure B, the cyclobutylsulfonyl chloride prepared in the step above was reacted with 5,6-difluoro-N1-(2-fluoro-4-iodopheny1)-3-methoxy-benzene-1,2-diamine to obtain the title product. Yield: 75%. 1H-NMR (300 MHz, CDC13):
8 = 7.44 (s, 1H, br), 7.41-7.36 (dd, 1H), 7.24-7.23 (m, 1H), 6.54-6.38 (m, 2H), 5.90 (s, 1H, br), 3.85-3.75 (m, 5H), 2.60-2.40 (m, 2H), 2.25-2.15 (m, 1H), 2.15-1.95 (m, 2H); m/z = 511 [MAI.
Example 62 N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)-6-methylpheny1)-1-(2,3-dihydroxypropyl)cyclopropane-l-sulfonamide:
Step A: (3,4,5-Trifluorophenyl)methanol:
HO
To a cooled (-5 C) solution of 3,4,5-trifluorobenzaldehyde (7.0 g, 43.75 mmol) in a mixture ( 50 ml, 9:1) of THF and water NaBH4 (1.662 g, 43.75 mmol) was slowly added in portions over a period of 30 min. The reaction mixture was allowed to attain room temperature over a period of 2h and carefully poured into ice-cold dil HC1 (200 ml, 1N). The oily layer was extracted into CH2C12 (250 ml) and the organic layer washed with water (200 ml), dried (MgSO4) and evaporated. The crude product (7.08 g, quantitative) obtained was taken forward without further purification.
Step B: 5-(Bromomethyl)-1,2,3-trifluorobenzene:
Br F
To a solution of the (3,4,5-Trifluorophenyl)methanol (40 mmol) in CH2C12 (150 ml), a solution of thionyl bromide (6.16 ml, 80 mmol) in CH2C12 (50 ml) was added slowly. The reaction mixture stirred at room temperature for 16h and poured into ice-water (200 ml). The organic layer was separated and washed with saturated NaHCO3 (2x200 ml), water (200 ml), dried (MgSO4) and evaporated to obtain the corresponding bromo compound as a pale yellow oil in quantitative yield. The crude product was carried forward for the next reaction without further purification.
Step C: 1,2,3-Trifluoro-5-methylbenzene:
The above bromo compound (40 mmol) was mixed with triethylsilane (48 mmol) and the reaction mixture was treated with solid PdC12 (4 mmol) in small portions.
After a few minutes a vigorous exothermic reaction was ensued and care was taken to reflux the contents of the flask by placing a reflux condenser. The reaction mixture was stirred at room temperature for additional 6h and the contents were allowed to settle over 16h. Then the crude liquid product was decanted carefully and carried forward for the next reaction without further purification. It was assumed tat the reaction proceeds in quantitative yield.
Step D: 1,2,3-Trifluoro-5-methy1-4-nitrobenzene:
HC ,F
1,2,3-Trifluoro-5-methylbenzene (40 mmol) was added to conc. H2SO4 (50 ml) at C. Then the reaction mixture was slowly treated with conc. HNO3 (3.39 ml, 48.44 mmol, 90%) while maintaining the internal temperature below 20 C. The reaction mixture was stirred at room temperature for 16h and poured onto ice (300 g) and the oily layer was extracted with CH2C12 (2x125 ml). The organic layer was washed with water (2x200 ml), brine (200 ml) and dried (MgSO4) and evaporated to obtain the crude product which was purified over flash silica gel chromatography to obtain the title product (6.5 g, 85%). 1H
NMR (300 MHz, CDC13): 8 6.96 (septet, 1H), 2.39 (s, 3H). 19F NMR (CDC13): 8 -128.18, -141.50, -159.05.
Step E: 2,3-Difluoro-N-(2-fluoro-4-iodopheny1)-5-methyl-6-nitroani1ine:
2-Fluoro-4-iodoaniline and 1,2,3-trifluoro-5-methy1-4-nitrobenzene were reacted using the condition described in Example 1 (Step A) to form the title compound. M-H+:
407.9 Step F: 5,6-Difluoro-N1-(2-fluoro-4-iodopheny1)-3-methylbenzene-1,2-diamine:
2,3-Difluoro-N-(2-fluoro-4-iodopheny1)-5-methy1-6-nitroaniline was reduced using the condition described in Example 1 (step B) to form the title compound. M-114.: 377.4 Step G: 1-Allyl-N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)-6-methylphenyl)cyclopropane-l-sulfonamide:
61:
According to the general procedure B, 1-allyl-cyclopropanesulfonyl chloride (142 mg, 142 mg) was reacted with 5,6-difluoro-N1-(2-fluoro-4-iodopheny1)-3-methylbenzene-1,2-diamine (150 mg, 0.4 mmole) to obtain the title product (100 mg, 47%); m/z =
521 [M-lf.
Step H: N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)-6-methylpheny1)-1-(2,3-dihydroxypropyl)cyclopropane-1-sulfonamide:
r...7H
HO ,p 0'19 NH H F
1-Allyl-N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)-6-methylphenyl) cyclopropane-l-sulfonamide ( 150 mg, 0.29 mmole) and 4-methylmorpholine N-oxide (33 mg, 0.29 mmole) was dissolved in THF (5 mL). Osmium tetroxide was added at room temperature (0.029 mmole, 0.18 mL, 4% in H20) and the reaction mixture was stirred at room temperature for 16 hours. Et0Ac was added, the organic phase was washed with water, dried (MgSO4) and concentrated under reduced pressure. The residue was purified over silica gel chromatography (eluants: Et0Ac/ Me0H) to obtain the titled product (0. 110 g, 68 %). 1H
NMR (300 MHz, CDC13): 8 7.07 (m, 1H), 6.97 (br m, 2H), 6.84 (m, 21-1), 6.60 (br m, 2H), 3.98 (br m, 1H), 3.58 (m, 1H), 3.43 (m, 1H), 3.20 (d, J= 3.9 Hz, 1H), 2.42 (s, 3H), 2.31 (dd, J= 9.9 & 15.6 Hz, 1H),2.01 (br t, 1H),2.31 (dd, J= 9.9 & 15.6 Hz, 1H), 1.66 (dd, J= 2.1 &
15.9 Hz, 1H), 1.52 (m, 1H), 1.40 (m, 1H), 0.91 (m, 2H).
Example 63 1-(2,3-Dihydroxypropy1)-N-(6-ethyl-3,4-difluoro-2-(2-tluoro-4-iodophenylamino) phenyl) cyclopropane-l-sulfonamide:
Step A: 1-(3,4,5-Trifluorophenypethanol:
An ethereal solution (17.41 ml, 52.24 mmol, 3M) of MeMgBr was slowly added at -78 C to a solution of 3,4,5-trifluorobenzaldehyde (6.96 g, 43.53 mmol) in THF
(125 m1). The reaction mixture was stirred at room temperature for 16h and was cooled (0 C) and was quenched, sequentially, with excess ethyl acetate (10 ml) and water (5 m1).
Excess anhydrous MgSO4 (5 g) was added and stirred for 30 minutes at room temperature. The suspension was filtered over celite and the solids were washed with ethyl acetate (2x25 m1).
The combined filtrate was evaporated to obtain the product in quantitative yield (7.65 g).
Step B: 5-(1-Bromoethy0-1,2,3-trifluorobenzene:
Br To a solution of the 1-(3,4,5-Trifluorophenyl)ethanol: (7.65 g, 43.5 mmol) in (250 ml), a solution of thionyl bromide (18.1 g, 87 mmol) in CH2C12 (50 ml) was added slowly. The reaction mixture stirred at room temperature for 16b and poured into ice-water (200 m1). The organic layer was separated and washed with saturated NaHCO3 (2x200 ml), water (200 ml), dried (MgSO4) and evaporated to obtain the corresponding bromo compound as a pale yellow oil in quantitative yield (10.4 g). The crude product was carried forward for the next reaction without further purification.
Step C: 5-Ethyl-1,2,3-trifluorobenzene:
F
The above bromo compound (9.65 g, 40.4 mmol) was mixed with triethylsilane (41 mmol) and the reaction mixture was treated with solid PdC12 (177 mg, 4 mmol) in small portions. After a few minutes a vigorous exothermic reaction was ensued and care was taken to reflux the contents of the flask by placing a reflux condenser. The reaction mixture was stirred at room temperature for additional 6h and the contents were allowed to settle over 16h.
Then the crude liquid product was decanted carefully and carried forward for the next reaction without further purification. It was assumed tat the reaction proceeds in quantitative yield.
Step D: 1 -Ethyl-3,4,5-trifluoro-2-nitrobenzene:
F
1,2,3-Trifluoro-5-methylbenzene (6.46 g, 40.4 mmol) was added to conc. H2SO4 (50 ml) at 0-5 C. Then the reaction mixture was slowly treated with conc. HNO3 (3.39 ml, 48.44 mmol, 90%) while maintaining the internal temperature below 20 C. The reaction mixture was stirred at room temperature for 16h and poured onto ice (300 g) and the oily layer was extracted with CH2C12 (2x125 ml). The organic layer was washed with water (2x200 ml), brine (200 ml) and dried (MgSO4) and evaporated to obtain the crude product which was purified over flash silica gel chromatography to obtain the title product (6.6 g, 79%). 111 NMR (CDC13): 6.98 (septet, 1H), 2.68 (q, 211), 1.26 (t, 7.8 & 7.2 Hz, 311).
Step E: 3-Ethyl-5,6-difluoro-N-(2-fluoro-4-iodopheny1)-2 nitroaniline:
2-Fluoro-4-iodoaniline (2.05 g, 10 mmole) and 1-ethy1-3,4,5-trifluoro-2-nitrobenzene (2.37 g, 10 mmole) were reacted using the condition described in example 1 (Step A) to form the title compound (2.47 g, 60%); nilz = 407 [M-1)".
Step F: 3-Ethyl-5,6-difluoro-N1-(2-fluoro-4-iodophenyl)benzene-1,2-diamine:
N
1,2,3-Trifluoro-5-methy1-4-nitrobenzene (2.47 g, 5.85 mmole) was reduced using the condition described in example 1 (Step B) to form the title compound. M-H+:
Step G: 1-Allyl-N-(6-ethy1-3,4-difluoro-2-(2-fluoro-4-iodophenylamino)phenyl)cyclopropane-l-sulfonamide:
r According to the general procedure B, 1-allyl-cyclopropanesulfonyl chloride (230 mg, 1.27 mmole) was reacted with 5,6-difluoro-N1-(2-fluoro-4-iodopheny1)-3-methylbenzene-1,2-diamine (100 mg, 0.255 mmole) to obtain the title product (72 mg, 53%);
771/Z = 535 [M-11".
Step H: 1-(2,3-Dihydroxypropy1)-N-(6-ethy1-3,4-difluoro-2-(2-fluoro-4-iodophenylamino)phenyl)cyclopropane-l-sulfonamide:
01 v....7H
HO ,p d'S 'NH H F
1-Allyl-N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)-6-methylphenyl) cyclopropane-1 -sulfonamide ( 70 mg, 0.13 mmole) and 4-methylmorpholine N-oxide (15 mg, 0.13 mmole) was dissolved in THF (2 mL). Osmium tetroxide was added at room temperature (0.013 mmole, 0.075 mL, 4% in H20) and the reaction mixture was stirred at room temperature for 16 hours. Et0Ac was added, the organic phase was washed with water, dried (MgSO4) and concentrated under reduced pressure. The residue was purified over silica gel chromatography (eluants: Et0Ac/ Me0H) to obtain the titled product. 1H NMR
(300 MHz, CDC13): 8 7.38 (dd, J= 2.1 & 10.8 Hz, 1H), 7.27 (m, 2H), 7.12 (br s, 1H), 6.91 (dd, J=
8.1 & 10.8 Hz, 1H), 6.69 (br s, 1H), 6.36 (dt, J= 4.8, 8.7 & 13.5 Hz, 1H), 4.00 (m, 1H), 3.62 (dd, J= 3.6 & 10.5 Hz, 1H), 3.47 (br m, 2H), 2.81 (q, 2H), 2.40 (dd, J= 10.2 &
15.9 Hz, 1H), 1.73 (br m, 2H), 1.58 (in, 1H), 1.43 (m, 111), 0.94 (m, 2H).
Example 64 N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)-6-(2-methoxyethoxy)pheny1)-1-(2,3-dihydroxypropyl)cyclopropane-1-sulfonamide:
Step A: 1,2,3-Trifluoro-5-(2-methoxyethoxy)-4-nitrobenzene:
To a mixture of 3,4,5-trifluoro-2-nitrophenol (1.93, 10 mmol), Ph3P (3.93 g, mmol), and 2-methoxy-ethanol (1.18 ml, 15 mmol) in anhydrous THF (25 ml) a solution of diisopropyl azodicarboxylate (2.91 ml, 15 mmol) in THF (5 ml) was added at 0 C and the reaction mixture was stirred at room temperature for 16h. The volatiles were evaporated and the residue was dissolved in CH2C12 (100 ml) and the organic layer was washed with water (100 ml), brine (100 ml) dried (MgSO4) and evaporated. The residue obtained was purified over flash silica gel chromatography to obtain the titled product in 68% (1.70 g) yield. 1H
NMR (300 MHz, CDC13): 8 6.78 (ddd, J= 2.4, 6.0, 11.7 Hz, 1H), 4.19 (t, J= 4.5 Hz, 2H), 3.72 (t, J= 4.5 Hz, 214), 3.39 (s, 3H).
Step B: 2,3-Difluoro-N-(2-fluoro-4-iodopheny1)-5-(2-methoxyethoxy)-6-nitroaniline:
2-Fluoro-4-iodoaniline (1.6 g, 6.8 mmole) and 1,2,3-trifluoro-5-(2-methoxyethoxy)-4-nitrobenzene (1.7 g, 6.8 mmole) were reacted using the condition described in Example 1 (Step A) to form the title compound (1.02 g, 32 %); m/z = 467 [M-11".
Step C: 5,6-Difluoro-N1-(2-fluoro-4-iodopheny1)-3-(2-methoxyethoxy)benzene-1,2-diamine:
-... ..--,, 0 0 N lei F I
F
2,3-Difluoro-N-(2-fluoro-4-iodopheny1)-5-(2-methoxyethoxy)-6-nitroaniline (1.017 g, 2.17 mmole) was reduced using the condition described in Example 1 (Step B) to form the title compound; m/z = 337 [M-1]-.
Step D: 1-Allyl-N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)-6-(2-methoxyethoxy)phenyl)cyclopropane-1-sulfonamide:
4rf Irjr, 13'-- 'NH F
H
OC) 0 F I
F
According to the general procedure B, 1-allyl-cyclopropanesulfonyl chloride (450 mg, 2.5 mmole) was reacted with 5,6-difluoro-N1-(2-fluoro-4-iodopheny1)-3-(2-methoxyethoxy)benzene-1,2-diamine (219 mg, 2.5 mmole) to obtain the title product (230 mg, 78%); m/z = 581 [M-lf..
Step E: N-(3 ,4-d ifluoro-2-(2-fluoro-4-iodophenylamino)-6-(2-methoxyethoxy)pheny1)-1-(2,3-dihydroxypropyl)cyclopropane-1-sulfonamide:
HOjJ,?
O''S NH H F
1-allyl-N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)-6-(2-methoxyethoxy) phenyl) cyclopropane-1-sulfonamide ( 230 mg, 0.395 mmole) and 4-methylmorpholine N-oxide (46 mg, 0.395 mmole) was dissolved in THF (2 mL). Osmium tetroxide was added at room temperature (0.039 mmole, 0.25 mL, 4% in H20) and the reaction mixture was stirred at room temperature for 16 hours. Et0Ac was added, the organic phase was washed with water, dried (MgSO4) and concentrated under reduced pressure. The residue was purified over silica gel chromatography (eluants: Et0Ac/ Me0H) to obtain the titled product. III
NMR (300 MHz, CDC13): 67.36 (dd, J= 1.8 & 10.5 Hz, 1H), 7.27 (m, 2H), 6.56 (dd, J= 6.9 & 11.4 Hz, 111), 6.40 (dt, J----- 5.7,7.5 & 12.9 Hz, 1H), 4.17 (m, 2H), 4.01 (m, 1H), 3.78 (m, 2H), 3.60 (dd, J= 3.6 & 11.1 Hz, 1H), 3.47 (m, 1H), 3.45 (s, 3H), 2.36 (dd, J= 9.6 &
15.9 Hz, 1H), 1.78 (dd, J= 2.4 & 15.6 Hz, 1H), 1.45-1.25 (m, 2H), 0.89 (m, 2H).
Example 65 2,4-diehloro-N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)phenyl) benzene sulfonamide:
CI lei CI
Is' NH
Synthesized by method A using the appropriate sulfonyl chloride. m/z --= 571 [M-1I.
Example 66 2-chloro-N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)pheny1)-4-(trifluoromethyl) benzenesulfonamide:
o Synthesized by method A using the appropriate sulfonyl chloride. inlz 605 [M-11`.
Example 67 N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)pheny1)-2-(trifluoromethoxy) benzene sulfonamide:
yF3 oo "NH H F
N
Synthesized by method A using the appropriate sulfonyl chloride. mth = 587 [M-1I.
Example 68 4-(N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)phenyl)sulfamoyl)benzoic acid:
HOOC
Si N
Synthesized by method A using the appropriate sulfonyl chloride. nilz = 584 [1\4-1f.
Example 69 N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)phenyl)benzenesulfonamide:
s, F
F I
F
Synthesized by method A using the appropriate sulfonyl chloride. m/z = 503 [M-lf.
Example 70 N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)phenyI)-2-fluorobenzene sulfonamide:
s, F
F I
F
Synthesized by method A using the appropriate sulfonyl chloride. m/z = 521 [M-11".
General procedure D: substitution of the iodine atom:
A suspension containing 1 eqv. aryl iodide, 1.5 equiv. of the boronic acid or boronic ester, 0.25 eqv. PdC12(dppf) x DCM and10 eqv. anhydrous K2CO3 powder in a deoxygenated mixture of dioxane and water (3:1) was heated in a microwave reactor for 60 min at 115 C.
It was extracted using aq. NH4C1/ THF, and the organic fraction was dried using Na2SO4.
The crude reaction products were purified using flash-column chromatography (Si, EtAc /
Hexanes, or CHCI3 / Me0H). Yields: 20-40%.
Example 71 N-(3,4-dffluoro-2-(2-fluoro-4-methylphenylamino)phenyl)cyclopropanesulfonamide;
,A, P
s, cr NH H F
F
General procedure D :1H-NMR (500 MHz, CDCI3): 8 = 7.38-7.36 (m, 1H), 7.06-7.03 (q, 1H), 6.92-6.90 (1H), 6.73-6.72 (d, 1H), 6.63 (s, 1H, br), 6.37-6.33 (t, 1H), 5.54 (s, 1H, br), 2.42-2.39 (m, 1H), 2.25 (s, 3H), 1.14-1.11 (m, 2H), 0.94-0.90 (m, 2H); mlz =
355 [M-ir.
Where racemic mixtures of chiral compounds have been resolved into separate enantiomers, the phrase "substantially free" of the epimer, as used herein, means an enantiomeric excess of at least 90%.
=
Biolvical activity Generation of ICSO Data Materials and preparation of reagents: Human GST-MEK1 and the constitutively active allele GST-MEK1cA (harboring the mutations Ser218Asp and Ser222Asp) were subcloned into the yeast expression vector pGEM4Z (Promega, Madison, WI) from the wild type human MEKI cDNA. GST-MEK1cA was expressed in Escherichia coil and partially purified using Glutathione Sepharose 4B affinity resin (Amersham Pharmacia Biotech, Piscataway, NJ). The ERK2 allele was subcloned from MAPK2/Erk2 cDNA (wild type) in pUSEamp (Upstate Biotechnology, Inc., Waltham, MA) into the vector pET2la (Novagen, Madison, WI) resulting in an N-terminal histidine-tagged mouse ERK2 allele.
ERK2 was expressed and purified to homogeneity. Myelin basic protein (MB?) was purchased from Gibco BRL (Rockville, MD). EasyTides adenosine 5'-triphosphate (ATP) (jy-33P}) (NEN Perkin Elmer, Wellesley, MA) was the source of radiolabel for all lcinase reactions. Activated Raf-1 (truncated) and activated MAPKinase 2/ERK2 were purchased TM
from Upstate, Inc. (Lake Placid, NY), 4-20% Criterion Precast gels were purchased from 1310-Rad (Hercules, CA).
Determination of enzymatic activity: Compounds were diluted from dimethylsulfoxide (DMSO) stocks into IxHMNDE (20 mM HEPES pH 7.2, 1 mM MgC12, 100 mM NaC1, 1.25 mM DTT, 0.2 mM EDTA). A typical 25-microliter assay contained 0.002 nanomoles MEK1cA, 0.02 nanomoles ERK2, 0.25 nanomoles MB?, 0.25 nanomoles unlabeled ATP, and 0.1 Ci Ey33133 ATP. The screening assay essentially comprised four additions. Five I of diluted compound were dispensed to 96-well assay plates.
Ten 1 of 2,5x enzyme cocktail (MEK1CA and ERK2 only) were then added to each well followed by a pre-incubation for 30 minutes at ambient temperature. Ten I of 2.5x substrate cocktail (labeled and unlabeled ATP plus MB?) were then added, followed by incubation for 60 minutes at ambient temperature. Finally, 100 id of 10% trichloroacetic acid (TCA) were added and incubated for 30 minutes at room temperature to halt the reaction and precipitate radiolabeled protein products. Reaction products were harvested on glass fiber 96 well filter plates prewetted with water and 1% pyrophosphate. The filter plate was then washed 5 times with water. Water was displaced by absolute ethanol and the plate was allowed to air dry for 30 minutes at room temperature. A back seal was applied manually and 40 pl of scintillation =
cocktail were dispensed to each well. A top seal was applied and the plate was counted in the TopCount for two seconds per well.
For certain experiments a truncated version of MEK that requires activation by Raf kinase were used.
Generation of EC5O Data Effects of compounds in the cell were determined by Western blotting for phosphorylated ERIC. MDA-MB-231 breast cancer cells were plated in a 48 well plate at 20,000 cells per well and grown in a 37 humidified CO2 incubator. The following day, the growth media (DMEM + 10% fetal bovine serum) was removed and replaced with starve media (DMEM + 0.1% fetal bovine serum). Cells were incubated in the starve media for sixteen hours and then treated with a range of compound concentrations for thirty minutes.
After incubation with compound, cells were stimulated with 10Onghnl EGF for five minutes.
The cells were then lysed and analyzed by Western blot using a monoclonal antibody raised to phosphorylated ERIC. The signal was amplified using a secondary antibody conjugated to a near -IR. dye and detected on a Licor OdysseyTm scanner. The intensity of signal was quantitated and this data was used to generate dose response curves and EC50 calculations.
Legend: A, EC50= < 2.0nM; B, EC50= 2.0-15nM; C, EC50 = 15nM-100nM;
D, EC50> 100nM, IC50 < 20 M; F, EC50> 100nM, 1050> 20 M
Compound Structure ACTIVITY pM
Number ei NH 001 1001 o N A
NH
Compound Structure ACTIVITY IJM
Number _ 1 i =''S
/'/ N
NH
SF' I
F
.--------,e C
NH
F I
F
s //N
F 0 NH so F I
F
(--i, S 6, 0 NH so F I
F
0 g F I
F
cl,õ0 s F I
F _ al F I
F
Compound Structure ACTIVITY pM
Number >(s/Y
NH =
I/
ON
--S
s NH
ak /5) o NH
NH
NH
el la eo NH
Compound Structure ACTIVITY pM
Number NH
NH
NH
NH
HO
(Racemic) A
If N
OH
1019 ,9 (Racemic) A
// N
NH
Compound Structure ACTIVITY 01 Number HO
(Racemic) 0 A
II
\NH
Ho F NH
OH
(R isomer) A
NH
pH
HO
(S isomer) szy // N
HO
HO,õ.
(R isomer) NH
F NH Is Compound Structure ACTIVITY pM
Number HO
2i)) (S isomer) NH
F NH
1025 n NH
Ao¨
NH
= 40 OH
s_+ A
--o¨
o¨
NH
si NH 401 OH OH
A
NH
Compound Structure ACTIVITY pM
Number \
NH
NH
1030 \
NH
SFSI
OH
\ A
NH
Claims (42)
1. A compound of formula I
where G is R1a, R1b, R1c, R1d, or R1e; R0 is H, halogen, CH3NH-, (CH3)2N-, C1-C6 alkyl, alkoxy, C3-C6 cycloalkyl, C2-C6 alkenyl, or C2-C6 alkynyl, said alkyl, alkoxy, cycloalkyl, alkenyl, and alkynyl groups optionally substituted with 1-3 substituents selected independently from the group consisting of halogen, OH, CN, cyanomethyl, nitro, phenyl, and trifluoromethyl, and said C1-C6 alkyl and C1-C4 alkoxy groups also optionally substituted with OCH3 or OCH2CH3; X is F, Cl, or methyl; Y is I, Br, Cl, CF3, C1-C3 alkyl, C2-C3 alkenyl, C2-C3 alkynyl, cyclopropyl, phenyl, pyridyl, pyrazolyl, OMe, OEt, or SMe, where said methyl group of X and said methyl, ethyl, C1-C3 alkyl, and cyclopropyl groups of Y
are optionally substituted with OH, where all said phenyl, pyridyl, and pyrazolyl groups of Y
are optionally substituted with halogen, acetyl, methyl, or trifluoromethyl, and where all said methyl groups of X and Y are optionally substituted with one, two, or three F atoms; and Z
is H or F;
where R1a is methyl, optionally substituted with 1-3 fluorine atoms or 1-3 chlorine atoms, or with OH, cyclopropoxy, or C1-C4 alkoxy, where said cyclopropoxy group or the C1-C4 alkyl moieties of said C1-C4 alkoxy groups are optionally substituted with one hydroxy or methoxy group, and where all C2-C4 alkyl groups within said C1-C4 alkoxy are optionally further substituted with a second OH group;
R1b is CH(CH3)-C1-3 alkyl or C3-C6 cycloalkyl, each of which is optionally substituted with 1-3 substituents selected independently from F, Cl, Br, I, OH, OCH3, and CN;
R1c is (CH2)n O m R', where m is 0 or 1; where, when m is 1, n is 2 or 3, and when m is 0, n is 1 or 2; and where R' is C1-C6 alkyl, optionally substituted with 1-3 substituents selected independently from F, CI, OH, OCH3, OCH2CH3, and C3-C6 cycloalkyl;
R1d is -C(A)(A')(B) where B, A, and A' are, independently, H or C14 alkyl, optionally substituted with one or two OH groups or halogen atoms, or A and A', together with the carbon atom to which they are attached, form a 3- to 6-member saturated ring, said ring optionally containing one or two heteroatoms selected, independently, from O, N, and S and optionally substituted with one or two groups selected independently from methyl, ethyl, and halo; and R1e is benzyl or 2-phenyl ethyl, in which the phenyl group is optionally substituted, as shown below:
where q is 1 or 2, R2, R3 and R4 are, independently, H, F, CI, Br, CH3, CH2F, CHF2, CF3, OCH3, OCH2F, OCHF2, OCF3, ethyl, n-propyl, isopropyl, cyclopropyl, isobutyl, sec-butyl, tert-butyl, or methylsulfonyl, and R4 may also be nitro, acetamido, amidinyl, cyano, carbamoyl, methylcarbamoyl, dimethylcarbamoyl, 1,3,4-oxadiazol-2-yl, 5-methyl-1,3,4-oxadiazol, 1,3,4-thiadiazol, 5-methyl-1,3,4-thiadiazol 1H-tetrazolyl, N-morpholyl carbonyl amino, N-morpholylsulfonyl or N-pyrrolidinylcarbonylamino; R5 and R6 are independently H, F, CI or methyl.
where G is R1a, R1b, R1c, R1d, or R1e; R0 is H, halogen, CH3NH-, (CH3)2N-, C1-C6 alkyl, alkoxy, C3-C6 cycloalkyl, C2-C6 alkenyl, or C2-C6 alkynyl, said alkyl, alkoxy, cycloalkyl, alkenyl, and alkynyl groups optionally substituted with 1-3 substituents selected independently from the group consisting of halogen, OH, CN, cyanomethyl, nitro, phenyl, and trifluoromethyl, and said C1-C6 alkyl and C1-C4 alkoxy groups also optionally substituted with OCH3 or OCH2CH3; X is F, Cl, or methyl; Y is I, Br, Cl, CF3, C1-C3 alkyl, C2-C3 alkenyl, C2-C3 alkynyl, cyclopropyl, phenyl, pyridyl, pyrazolyl, OMe, OEt, or SMe, where said methyl group of X and said methyl, ethyl, C1-C3 alkyl, and cyclopropyl groups of Y
are optionally substituted with OH, where all said phenyl, pyridyl, and pyrazolyl groups of Y
are optionally substituted with halogen, acetyl, methyl, or trifluoromethyl, and where all said methyl groups of X and Y are optionally substituted with one, two, or three F atoms; and Z
is H or F;
where R1a is methyl, optionally substituted with 1-3 fluorine atoms or 1-3 chlorine atoms, or with OH, cyclopropoxy, or C1-C4 alkoxy, where said cyclopropoxy group or the C1-C4 alkyl moieties of said C1-C4 alkoxy groups are optionally substituted with one hydroxy or methoxy group, and where all C2-C4 alkyl groups within said C1-C4 alkoxy are optionally further substituted with a second OH group;
R1b is CH(CH3)-C1-3 alkyl or C3-C6 cycloalkyl, each of which is optionally substituted with 1-3 substituents selected independently from F, Cl, Br, I, OH, OCH3, and CN;
R1c is (CH2)n O m R', where m is 0 or 1; where, when m is 1, n is 2 or 3, and when m is 0, n is 1 or 2; and where R' is C1-C6 alkyl, optionally substituted with 1-3 substituents selected independently from F, CI, OH, OCH3, OCH2CH3, and C3-C6 cycloalkyl;
R1d is -C(A)(A')(B) where B, A, and A' are, independently, H or C14 alkyl, optionally substituted with one or two OH groups or halogen atoms, or A and A', together with the carbon atom to which they are attached, form a 3- to 6-member saturated ring, said ring optionally containing one or two heteroatoms selected, independently, from O, N, and S and optionally substituted with one or two groups selected independently from methyl, ethyl, and halo; and R1e is benzyl or 2-phenyl ethyl, in which the phenyl group is optionally substituted, as shown below:
where q is 1 or 2, R2, R3 and R4 are, independently, H, F, CI, Br, CH3, CH2F, CHF2, CF3, OCH3, OCH2F, OCHF2, OCF3, ethyl, n-propyl, isopropyl, cyclopropyl, isobutyl, sec-butyl, tert-butyl, or methylsulfonyl, and R4 may also be nitro, acetamido, amidinyl, cyano, carbamoyl, methylcarbamoyl, dimethylcarbamoyl, 1,3,4-oxadiazol-2-yl, 5-methyl-1,3,4-oxadiazol, 1,3,4-thiadiazol, 5-methyl-1,3,4-thiadiazol 1H-tetrazolyl, N-morpholyl carbonyl amino, N-morpholylsulfonyl or N-pyrrolidinylcarbonylamino; R5 and R6 are independently H, F, CI or methyl.
2. The compound of claim 1, where X is F, CI, or CH3: Y is I, Br, Cl, CF3, or C1-C3 alkyl; and Z is H or F.
3. The compound of claim 1, where R0 is F, Cl, C1-C4 alkyl or C1-4alkoxy, said C1-C4 alkyl group and the C1-C4 alkyl moiety of said C1-C4 alkoxy group optionally substituted with F, CI, OCH3, or OCH2CH3.
4. The compound of claim 2, where R o is H, F, Cl, C1-C4 alkyl, methoxy, ethoxy, or 2-methoxy-ethoxy.
5. The compound of claim 4 where G is Ria and Z is F.
6. The compound of claim 5, where G is CH3; R o is H; and Y is Br, I, CF3, or CH3.
7. The compound of any one of claims 1 to 4, where G is R1b-
8. The compound of claim 4 where G is R1b and Z is F.
9. The compound of claim 8, where R 0 is H, F, or OCH3, X is F or CH3, and Y is Br, I, or CH3.
10. The compound of claim 9, where G is unsubstituted C3-C6 cycloalkyl.
11. The compound of claim 10, where R o is H.
12. The compound of claim 9, where G is isopropyl or cyclopropyl.
13. The compound of any one of claims 1 to 4, where G is R1c.
14. The compound of claim 4, where G is R1c, Y is I, Br, CH3, or CF3; and Z
is F.
is F.
15. The compound of claim 14, where m is zero.
16. The compound of any one of claims 1 to 4, where G is R1d.
17. The compound of claim 1, where G is R1d; R o is fluoro, chloro, methyl, ethyl, propyl, isopropyl, sec-butyl, iso-butyl, tert-butyl, cyclopropyl, cyclobutyl, fluoromethyl, methoxy, fluoromethoxy, methylamino or dimethylamino; X is F, Cl, CH3, or mono-, di- or tri-fluoromethyl; Y is I, Br, Cl, or mono-, di- or tri-fluoromethyl; and Z is H or F.
18. The compound of claim 1, where G is R1d; R o is F, Cl, methyl, ethyl, methoxy, ethoxy, or 2-methoxy-ethoxy; X is F, Cl, or CH3; Y is I, Br, Cl, or mono-, di-or tri-fluoromethyl; and Z is H or F.
19. The compound of claim 1, where G is R1d; R0 is H; X is F, CI, CH3, or mono-, di- or tri-fluoromethyl; Y is I, Br, CI, or mono-, di- or tri-fluoromethyl;
and Z is H or F.
and Z is H or F.
20. The compound of any one of claims 17-19, where C(A)(A') is C3-C6 cycloalkyl.
21. The compound of claim 20, where B is H.
22. The compound of claim 21, where C(A)(A') is cyclopropyl.
23. The compound of claim 20, where B is methyl, optionally substituted with one OH group, or C2-C4 alkyl, optionally substituted with one or two OH groups.
24. The compound of claim 23, where C(A)(A') is cyclopropyl.
25. The compound of claim 24, where B is methyl, ethyl, 2-hydroxyethyl, n-propyl, 3-hydroxypropyl, 2,3-dihydroxypropyl, 3,4-dihydroxybutyl, isopropyl, 1-methyl-2-hydroxy ethyl, n-butyl, sec-butyl, isobutyl, or 2-hydroxymethyl-3-hydroxy propyl.
26. The compound of claim 25, where B is 2,3-dihydroxypropyl or 3,4-dihydroxybutyl.
27. The compound of claim 26, in which the chiral carbon in B is in the R
configuration.
configuration.
28. The compound of any one of claims 1 to 4, where G is R1e.
29. The compound of claim 28, where q is 1.
30. The compound of claim 29, where R0 is H, R4-6are H; R2 and R3 are, independently, H, F, CI, Br, CH3, CH2F, CHF2, CF3, OCH3, OCH2F, OCHF2, OCF3, ethyl, n-propyl, isopropyl, cyclopropyl, isobutyl, sec-butyl, tert-butyl, or methylsulfonyl; X is F and Y is I.
31. A compound which is selected from the compounds below
32. A compound which is:
where the 2-OH carbon is in the R or S configuration.
where the 2-OH carbon is in the R or S configuration.
33. (S)-N-(3,4-difluoro-2-(2-fluoro-4-iodophenylamino)-6-methoxyphenyl)-1-(2,3-dihydroxypropyl)cyclopropane-1-sulfonamide.
34. A pharmaceutical composition comprising a compound of formula I
according to any one of claims 1 to 33, or a pharmaceutically acceptable salt, ester, or hydrate thereof, and a pharmaceutically acceptable carrier.
according to any one of claims 1 to 33, or a pharmaceutically acceptable salt, ester, or hydrate thereof, and a pharmaceutically acceptable carrier.
35. A pharmaceutical composition comprising the compound:
or a pharmaceutically acceptable salt, ester, or hydrate thereof, and a pharmaceutically acceptable carrier.
or a pharmaceutically acceptable salt, ester, or hydrate thereof, and a pharmaceutically acceptable carrier.
36. The composition of claim 35, where the compound is in the R or S
configuration.
configuration.
37. A pharmaceutical composition comprising (S)-N-(3,4-difluoro-2-(2-fluoro-iodophenylamino)-6-methoxyphenyl)-1-(2,3-dihydroxypropyl)cyclopropane-1-sulfonamide, and a pharmaceutically acceptable carrier.
38. A composition comprising a compound according to claim 33, and a pharmaceutically acceptable carrier, which composition is substantially free of the R isomer.
39. A composition comprising the compound shown below, where the 2-OH carbon is in the S configuration, and a pharmaceutically acceptable carrier, wherein the composition is substantially free of the R-isomer.
40. Use of a compound as defined in any one of claims 1 to 33 for the inhibition of MEK.
41. Use according to claim 40, wherein the MEK is MEK1.
42. Use according to claim 40, wherein the MEK is MEK2.
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US60/701,814 | 2005-07-21 | ||
US70671905P | 2005-08-08 | 2005-08-08 | |
US60/706,719 | 2005-08-08 | ||
US73163305P | 2005-10-28 | 2005-10-28 | |
US60/731,633 | 2005-10-28 | ||
PCT/US2006/028326 WO2007014011A2 (en) | 2005-07-21 | 2006-07-21 | N-(arylamino)-sulfonamide inhibitors of mek |
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KR (1) | KR101377688B1 (en) |
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CY (1) | CY1118055T1 (en) |
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US20040171632A1 (en) * | 1998-12-22 | 2004-09-02 | Gowan Richard Carleton | Combination chemotherapy |
CA2349832A1 (en) * | 1999-01-13 | 2000-07-20 | Warner-Lambert Company | Benzenesulfonamide derivatives and their use as mek inhibitors |
EP1598079B1 (en) | 2003-02-26 | 2009-04-22 | Kowa Co., Ltd. | Remedies for allergic contact dermatitis |
TW200505834A (en) | 2003-03-18 | 2005-02-16 | Sankyo Co | Sulfamide derivative and the pharmaceutical composition thereof |
US7538120B2 (en) | 2003-09-03 | 2009-05-26 | Array Biopharma Inc. | Method of treating inflammatory diseases |
MXPA06014478A (en) * | 2004-06-11 | 2007-03-21 | Japan Tobacco Inc | 5-amino-2,4,7-trioxo-3,4,7,8-tetrahydro-2h-pyrido'2,3-d! pyrimidine derivatives and related compounds for the treatment of cancer. |
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IL189201A0 (en) | 2009-02-11 |
CA2618218A1 (en) | 2007-02-01 |
KR101377688B1 (en) | 2014-03-25 |
CY1118055T1 (en) | 2017-06-28 |
WO2007014011A3 (en) | 2009-04-23 |
AU2006272837A1 (en) | 2007-02-01 |
EP1912636A2 (en) | 2008-04-23 |
EP1912636A4 (en) | 2009-11-18 |
DK1912636T3 (en) | 2014-07-21 |
KR20080068637A (en) | 2008-07-23 |
MX2008002114A (en) | 2008-04-17 |
WO2007014011A2 (en) | 2007-02-01 |
HK1134436A1 (en) | 2010-04-30 |
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