AP805A - Process for substituted pyridines. - Google Patents
Process for substituted pyridines. Download PDFInfo
- Publication number
- AP805A AP805A APAP/P/1997/001147A AP9701147A AP805A AP 805 A AP805 A AP 805A AP 9701147 A AP9701147 A AP 9701147A AP 805 A AP805 A AP 805A
- Authority
- AP
- ARIPO
- Prior art keywords
- alkyl
- compound
- independently
- formula
- group
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims abstract description 55
- 230000008569 process Effects 0.000 title claims abstract description 47
- 150000003222 pyridines Chemical class 0.000 title description 3
- 150000001875 compounds Chemical class 0.000 claims abstract description 245
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 179
- -1 nitro, amino Chemical group 0.000 claims abstract description 102
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims abstract description 79
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims abstract description 60
- 125000003545 alkoxy group Chemical group 0.000 claims abstract description 58
- 125000001153 fluoro group Chemical group F* 0.000 claims abstract description 30
- 125000005843 halogen group Chemical group 0.000 claims description 117
- 229910052739 hydrogen Inorganic materials 0.000 claims description 111
- 239000001257 hydrogen Substances 0.000 claims description 92
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical group N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 75
- 238000006243 chemical reaction Methods 0.000 claims description 69
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 62
- 229910052760 oxygen Inorganic materials 0.000 claims description 56
- 229910052757 nitrogen Inorganic materials 0.000 claims description 55
- 229910052717 sulfur Chemical group 0.000 claims description 54
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 47
- 239000001301 oxygen Substances 0.000 claims description 47
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 45
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 45
- 239000011593 sulfur Chemical group 0.000 claims description 45
- 239000000203 mixture Substances 0.000 claims description 43
- 125000004432 carbon atom Chemical group C* 0.000 claims description 38
- 125000000623 heterocyclic group Chemical group 0.000 claims description 36
- 125000001424 substituent group Chemical group 0.000 claims description 32
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 26
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 26
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 25
- 239000012442 inert solvent Substances 0.000 claims description 25
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims description 24
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 24
- HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 claims description 23
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 23
- 229910052799 carbon Inorganic materials 0.000 claims description 20
- 238000004519 manufacturing process Methods 0.000 claims description 19
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 17
- 239000003446 ligand Substances 0.000 claims description 16
- 125000006242 amine protecting group Chemical group 0.000 claims description 15
- SYQBFIAQOQZEGI-UHFFFAOYSA-N osmium atom Chemical compound [Os] SYQBFIAQOQZEGI-UHFFFAOYSA-N 0.000 claims description 15
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 14
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 13
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 12
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims description 12
- RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 claims description 12
- 239000003054 catalyst Substances 0.000 claims description 12
- 239000011260 aqueous acid Substances 0.000 claims description 10
- KWGKDLIKAYFUFQ-UHFFFAOYSA-M lithium chloride Chemical group [Li+].[Cl-] KWGKDLIKAYFUFQ-UHFFFAOYSA-M 0.000 claims description 10
- 230000003287 optical effect Effects 0.000 claims description 10
- 230000000269 nucleophilic effect Effects 0.000 claims description 9
- 239000007800 oxidant agent Substances 0.000 claims description 9
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 claims description 8
- 150000002431 hydrogen Chemical group 0.000 claims description 8
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 8
- 229910052762 osmium Inorganic materials 0.000 claims description 8
- ZFTFAPZRGNKQPU-UHFFFAOYSA-N dicarbonic acid Chemical compound OC(=O)OC(O)=O ZFTFAPZRGNKQPU-UHFFFAOYSA-N 0.000 claims description 7
- DLFVBJFMPXGRIB-UHFFFAOYSA-N Acetamide Chemical compound CC(N)=O DLFVBJFMPXGRIB-UHFFFAOYSA-N 0.000 claims description 6
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical group C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 claims description 6
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 6
- 150000002907 osmium Chemical class 0.000 claims description 6
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims description 5
- YUCBLVFHJWOYDN-HVLQGHBFSA-N 1,4-bis[(s)-[(2r,4s,5r)-5-ethyl-1-azabicyclo[2.2.2]octan-2-yl]-(6-methoxyquinolin-4-yl)methoxy]phthalazine Chemical compound C1=C(OC)C=C2C([C@H](OC=3C4=CC=CC=C4C(O[C@H]([C@@H]4N5CC[C@H]([C@H](C5)CC)C4)C=4C5=CC(OC)=CC=C5N=CC=4)=NN=3)[C@H]3C[C@@H]4CCN3C[C@@H]4CC)=CC=NC2=C1 YUCBLVFHJWOYDN-HVLQGHBFSA-N 0.000 claims description 5
- 150000001721 carbon Chemical group 0.000 claims description 5
- 239000012320 chlorinating reagent Substances 0.000 claims description 5
- LSBDFXRDZJMBSC-UHFFFAOYSA-N 2-phenylacetamide Chemical compound NC(=O)CC1=CC=CC=C1 LSBDFXRDZJMBSC-UHFFFAOYSA-N 0.000 claims description 4
- YUCBLVFHJWOYDN-PPIALRKJSA-N 4-[(r)-[(2r,4s,5r)-5-ethyl-1-azabicyclo[2.2.2]octan-2-yl]-(6-methoxyquinolin-4-yl)methoxy]-1-[(r)-[(2r,4r,5s)-5-ethyl-1-azabicyclo[2.2.2]octan-2-yl]-(6-methoxyquinolin-4-yl)methoxy]phthalazine Chemical compound C1=C(OC)C=C2C([C@@H](OC=3C4=CC=CC=C4C(O[C@@H]([C@@H]4N5CC[C@@H]([C@@H](C5)CC)C4)C=4C5=CC(OC)=CC=C5N=CC=4)=NN=3)[C@H]3C[C@@H]4CCN3C[C@@H]4CC)=CC=NC2=C1 YUCBLVFHJWOYDN-PPIALRKJSA-N 0.000 claims description 4
- 125000000738 acetamido group Chemical group [H]C([H])([H])C(=O)N([H])[*] 0.000 claims description 4
- 125000001246 bromo group Chemical group Br* 0.000 claims description 4
- 125000002346 iodo group Chemical group I* 0.000 claims description 4
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims description 3
- NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 claims description 3
- 150000008065 acid anhydrides Chemical class 0.000 claims description 3
- 125000004414 alkyl thio group Chemical group 0.000 claims description 3
- 229910052740 iodine Inorganic materials 0.000 claims description 3
- 125000005951 trifluoromethanesulfonyloxy group Chemical group 0.000 claims description 3
- 125000000008 (C1-C10) alkyl group Chemical group 0.000 claims description 2
- 125000004105 2-pyridyl group Chemical group N1=C([*])C([H])=C([H])C([H])=C1[H] 0.000 claims description 2
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 claims description 2
- 125000003282 alkyl amino group Chemical group 0.000 claims description 2
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 claims description 2
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims 1
- 239000000543 intermediate Substances 0.000 abstract description 5
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 87
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 61
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 48
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 30
- 239000002585 base Substances 0.000 description 30
- 239000000243 solution Substances 0.000 description 29
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 28
- 239000000047 product Substances 0.000 description 25
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 24
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 24
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 24
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 24
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 23
- 239000007787 solid Substances 0.000 description 23
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 21
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 18
- 239000002904 solvent Substances 0.000 description 18
- 238000005160 1H NMR spectroscopy Methods 0.000 description 16
- 229960004592 isopropanol Drugs 0.000 description 16
- 239000011541 reaction mixture Substances 0.000 description 15
- 239000003153 chemical reaction reagent Substances 0.000 description 14
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 13
- 239000000758 substrate Substances 0.000 description 13
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 12
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 12
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 12
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 12
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 12
- 238000003756 stirring Methods 0.000 description 12
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 10
- 239000002253 acid Substances 0.000 description 10
- 239000000808 adrenergic beta-agonist Substances 0.000 description 10
- 239000013078 crystal Substances 0.000 description 10
- 239000010410 layer Substances 0.000 description 10
- 238000002360 preparation method Methods 0.000 description 10
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 9
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 9
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 8
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 8
- 150000001412 amines Chemical class 0.000 description 8
- 239000012267 brine Substances 0.000 description 8
- NOESYZHRGYRDHS-UHFFFAOYSA-N insulin Chemical compound N1C(=O)C(NC(=O)C(CCC(N)=O)NC(=O)C(CCC(O)=O)NC(=O)C(C(C)C)NC(=O)C(NC(=O)CN)C(C)CC)CSSCC(C(NC(CO)C(=O)NC(CC(C)C)C(=O)NC(CC=2C=CC(O)=CC=2)C(=O)NC(CCC(N)=O)C(=O)NC(CC(C)C)C(=O)NC(CCC(O)=O)C(=O)NC(CC(N)=O)C(=O)NC(CC=2C=CC(O)=CC=2)C(=O)NC(CSSCC(NC(=O)C(C(C)C)NC(=O)C(CC(C)C)NC(=O)C(CC=2C=CC(O)=CC=2)NC(=O)C(CC(C)C)NC(=O)C(C)NC(=O)C(CCC(O)=O)NC(=O)C(C(C)C)NC(=O)C(CC(C)C)NC(=O)C(CC=2NC=NC=2)NC(=O)C(CO)NC(=O)CNC2=O)C(=O)NCC(=O)NC(CCC(O)=O)C(=O)NC(CCCNC(N)=N)C(=O)NCC(=O)NC(CC=3C=CC=CC=3)C(=O)NC(CC=3C=CC=CC=3)C(=O)NC(CC=3C=CC(O)=CC=3)C(=O)NC(C(C)O)C(=O)N3C(CCC3)C(=O)NC(CCCCN)C(=O)NC(C)C(O)=O)C(=O)NC(CC(N)=O)C(O)=O)=O)NC(=O)C(C(C)CC)NC(=O)C(CO)NC(=O)C(C(C)O)NC(=O)C1CSSCC2NC(=O)C(CC(C)C)NC(=O)C(NC(=O)C(CCC(N)=O)NC(=O)C(CC(N)=O)NC(=O)C(NC(=O)C(N)CC=1C=CC=CC=1)C(C)C)CC1=CN=CN1 NOESYZHRGYRDHS-UHFFFAOYSA-N 0.000 description 8
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 8
- GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 8
- 239000000725 suspension Substances 0.000 description 8
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 7
- 230000015572 biosynthetic process Effects 0.000 description 7
- 150000002924 oxiranes Chemical class 0.000 description 7
- 150000003254 radicals Chemical class 0.000 description 7
- 150000003839 salts Chemical class 0.000 description 7
- 238000011282 treatment Methods 0.000 description 7
- YYROPELSRYBVMQ-UHFFFAOYSA-N 4-toluenesulfonyl chloride Chemical compound CC1=CC=C(S(Cl)(=O)=O)C=C1 YYROPELSRYBVMQ-UHFFFAOYSA-N 0.000 description 6
- XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 description 6
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 6
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 6
- JFDZBHWFFUWGJE-UHFFFAOYSA-N benzonitrile Chemical compound N#CC1=CC=CC=C1 JFDZBHWFFUWGJE-UHFFFAOYSA-N 0.000 description 6
- 239000003795 chemical substances by application Substances 0.000 description 6
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 6
- 239000000706 filtrate Substances 0.000 description 6
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical class CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 6
- YJVFFLUZDVXJQI-UHFFFAOYSA-L palladium(ii) acetate Chemical compound [Pd+2].CC([O-])=O.CC([O-])=O YJVFFLUZDVXJQI-UHFFFAOYSA-L 0.000 description 6
- 239000002002 slurry Substances 0.000 description 6
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 6
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 5
- 239000005977 Ethylene Substances 0.000 description 5
- 238000005481 NMR spectroscopy Methods 0.000 description 5
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 5
- 230000004913 activation Effects 0.000 description 5
- 102000012740 beta Adrenergic Receptors Human genes 0.000 description 5
- 108010079452 beta Adrenergic Receptors Proteins 0.000 description 5
- LJOQGZACKSYWCH-UHFFFAOYSA-N dihydro quinine Natural products C1=C(OC)C=C2C(C(O)C3CC4CCN3CC4CC)=CC=NC2=C1 LJOQGZACKSYWCH-UHFFFAOYSA-N 0.000 description 5
- LJOQGZACKSYWCH-WZBLMQSHSA-N hydroquinine Chemical compound C1=C(OC)C=C2C([C@@H](O)[C@@H]3C[C@@H]4CCN3C[C@@H]4CC)=CC=NC2=C1 LJOQGZACKSYWCH-WZBLMQSHSA-N 0.000 description 5
- 239000002798 polar solvent Substances 0.000 description 5
- 239000002244 precipitate Substances 0.000 description 5
- 125000006239 protecting group Chemical group 0.000 description 5
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 5
- 238000001953 recrystallisation Methods 0.000 description 5
- 238000010992 reflux Methods 0.000 description 5
- 229910052938 sodium sulfate Inorganic materials 0.000 description 5
- 235000011152 sodium sulphate Nutrition 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- 238000003786 synthesis reaction Methods 0.000 description 5
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 4
- IAZDPXIOMUYVGZ-WFGJKAKNSA-N Dimethyl sulfoxide Chemical group [2H]C([2H])([2H])S(=O)C([2H])([2H])[2H] IAZDPXIOMUYVGZ-WFGJKAKNSA-N 0.000 description 4
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 4
- 102000004877 Insulin Human genes 0.000 description 4
- 108090001061 Insulin Proteins 0.000 description 4
- JGFZNNIVVJXRND-UHFFFAOYSA-N N,N-Diisopropylethylamine (DIPEA) Chemical compound CCN(C(C)C)C(C)C JGFZNNIVVJXRND-UHFFFAOYSA-N 0.000 description 4
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 4
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 4
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- 150000001336 alkenes Chemical class 0.000 description 4
- 239000008346 aqueous phase Substances 0.000 description 4
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 4
- 239000008280 blood Substances 0.000 description 4
- 210000004369 blood Anatomy 0.000 description 4
- 206010012601 diabetes mellitus Diseases 0.000 description 4
- DGODWNOPHMXOTR-UHFFFAOYSA-N dipotassium;dioxido(dioxo)osmium;dihydrate Chemical compound O.O.[K+].[K+].[O-][Os]([O-])(=O)=O DGODWNOPHMXOTR-UHFFFAOYSA-N 0.000 description 4
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 239000000284 extract Substances 0.000 description 4
- 229960004251 hydroquinine Drugs 0.000 description 4
- 229940125396 insulin Drugs 0.000 description 4
- 229910052763 palladium Inorganic materials 0.000 description 4
- 229910000027 potassium carbonate Inorganic materials 0.000 description 4
- 235000011181 potassium carbonates Nutrition 0.000 description 4
- 239000000741 silica gel Substances 0.000 description 4
- 229910002027 silica gel Inorganic materials 0.000 description 4
- 235000010265 sodium sulphite Nutrition 0.000 description 4
- 239000007858 starting material Substances 0.000 description 4
- 230000002194 synthesizing effect Effects 0.000 description 4
- 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 4
- 239000008096 xylene Substances 0.000 description 4
- OISVCGZHLKNMSJ-UHFFFAOYSA-N 2,6-dimethylpyridine Chemical compound CC1=CC=CC(C)=N1 OISVCGZHLKNMSJ-UHFFFAOYSA-N 0.000 description 3
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- XMJHPCRAQCTCFT-UHFFFAOYSA-N methyl chloroformate Chemical compound COC(Cl)=O XMJHPCRAQCTCFT-UHFFFAOYSA-N 0.000 description 1
- XYBRWUNZRUBCGY-UHFFFAOYSA-N methyl n-(5-bromopyridin-2-yl)carbamate Chemical compound COC(=O)NC1=CC=C(Br)C=N1 XYBRWUNZRUBCGY-UHFFFAOYSA-N 0.000 description 1
- ZFIULJUUXQPOQO-UHFFFAOYSA-N n-(3-ethenylpyridin-2-yl)acetamide Chemical compound CC(=O)NC1=NC=CC=C1C=C ZFIULJUUXQPOQO-UHFFFAOYSA-N 0.000 description 1
- LHJMFFKVXROWOC-UHFFFAOYSA-N n-(5-bromopyridin-2-yl)-2,2-dimethylpropanamide Chemical compound CC(C)(C)C(=O)NC1=CC=C(Br)C=N1 LHJMFFKVXROWOC-UHFFFAOYSA-N 0.000 description 1
- MJFCOXATGBYERZ-UHFFFAOYSA-N n-(5-bromopyridin-2-yl)acetamide Chemical compound CC(=O)NC1=CC=C(Br)C=N1 MJFCOXATGBYERZ-UHFFFAOYSA-N 0.000 description 1
- DUSUDDSKKLCVMN-UHFFFAOYSA-N n-(5-ethenylpyridin-2-yl)-2,2-dimethylpropanamide Chemical compound CC(C)(C)C(=O)NC1=CC=C(C=C)C=N1 DUSUDDSKKLCVMN-UHFFFAOYSA-N 0.000 description 1
- ZMFMQXXDCVDWFI-UHFFFAOYSA-N n-(5-ethenylpyridin-2-yl)acetamide Chemical compound CC(=O)NC1=CC=C(C=C)C=N1 ZMFMQXXDCVDWFI-UHFFFAOYSA-N 0.000 description 1
- DUTJLVHVDAXHDN-QMMMGPOBSA-N n-[5-[(1r)-1,2-dihydroxyethyl]pyridin-2-yl]acetamide Chemical compound CC(=O)NC1=CC=C([C@@H](O)CO)C=N1 DUTJLVHVDAXHDN-QMMMGPOBSA-N 0.000 description 1
- WAXONIBXUBSLKF-QMMMGPOBSA-N n-[5-[(1r)-2-chloro-1-hydroxyethyl]pyridin-2-yl]acetamide Chemical compound CC(=O)NC1=CC=C([C@@H](O)CCl)C=N1 WAXONIBXUBSLKF-QMMMGPOBSA-N 0.000 description 1
- DUTJLVHVDAXHDN-MRVPVSSYSA-N n-[5-[(1s)-1,2-dihydroxyethyl]pyridin-2-yl]acetamide Chemical compound CC(=O)NC1=CC=C([C@H](O)CO)C=N1 DUTJLVHVDAXHDN-MRVPVSSYSA-N 0.000 description 1
- CJZFSTRFUHALFT-QMMMGPOBSA-N n-[5-[(2r)-oxiran-2-yl]pyridin-2-yl]acetamide Chemical compound C1=NC(NC(=O)C)=CC=C1[C@H]1OC1 CJZFSTRFUHALFT-QMMMGPOBSA-N 0.000 description 1
- LWFWUJCJKPUZLV-UHFFFAOYSA-N n-trimethylsilylacetamide Chemical compound CC(=O)N[Si](C)(C)C LWFWUJCJKPUZLV-UHFFFAOYSA-N 0.000 description 1
- 238000010899 nucleation Methods 0.000 description 1
- 239000012038 nucleophile Substances 0.000 description 1
- 239000012044 organic layer Substances 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 125000000914 phenoxymethylpenicillanyl group Chemical group CC1(S[C@H]2N([C@H]1C(=O)*)C([C@H]2NC(COC2=CC=CC=C2)=O)=O)C 0.000 description 1
- UYWQUFXKFGHYNT-UHFFFAOYSA-N phenylmethyl ester of formic acid Natural products O=COCC1=CC=CC=C1 UYWQUFXKFGHYNT-UHFFFAOYSA-N 0.000 description 1
- 229960005235 piperonyl butoxide Drugs 0.000 description 1
- 230000000291 postprandial effect Effects 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 239000011736 potassium bicarbonate Substances 0.000 description 1
- 235000015497 potassium bicarbonate Nutrition 0.000 description 1
- 229910000028 potassium bicarbonate Inorganic materials 0.000 description 1
- VKJKEPKFPUWCAS-UHFFFAOYSA-M potassium chlorate Chemical compound [K+].[O-]Cl(=O)=O VKJKEPKFPUWCAS-UHFFFAOYSA-M 0.000 description 1
- TYJJADVDDVDEDZ-UHFFFAOYSA-M potassium hydrogencarbonate Chemical compound [K+].OC([O-])=O TYJJADVDDVDEDZ-UHFFFAOYSA-M 0.000 description 1
- 239000012286 potassium permanganate Substances 0.000 description 1
- USHAGKDGDHPEEY-UHFFFAOYSA-L potassium persulfate Chemical compound [K+].[K+].[O-]S(=O)(=O)OOS([O-])(=O)=O USHAGKDGDHPEEY-UHFFFAOYSA-L 0.000 description 1
- LPNYRYFBWFDTMA-UHFFFAOYSA-N potassium tert-butoxide Chemical compound [K+].CC(C)(C)[O-] LPNYRYFBWFDTMA-UHFFFAOYSA-N 0.000 description 1
- 230000002265 prevention 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
- 125000002572 propoxy group Chemical group [*]OC([H])([H])C(C([H])([H])[H])([H])[H] 0.000 description 1
- 238000010926 purge Methods 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 239000000018 receptor agonist Substances 0.000 description 1
- 229940044601 receptor agonist Drugs 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 230000012501 relaxation of skeletal muscle Effects 0.000 description 1
- 238000007363 ring formation reaction Methods 0.000 description 1
- 150000003335 secondary amines Chemical class 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- CLDWGXZGFUNWKB-UHFFFAOYSA-M silver;benzoate Chemical compound [Ag+].[O-]C(=O)C1=CC=CC=C1 CLDWGXZGFUNWKB-UHFFFAOYSA-M 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 235000017550 sodium carbonate Nutrition 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 239000012312 sodium hydride Substances 0.000 description 1
- 229910000104 sodium hydride Inorganic materials 0.000 description 1
- 239000011877 solvent mixture Substances 0.000 description 1
- 230000000707 stereoselective effect Effects 0.000 description 1
- 239000012258 stirred mixture Substances 0.000 description 1
- 125000005504 styryl group Chemical group 0.000 description 1
- GFYHSKONPJXCDE-UHFFFAOYSA-N sym-collidine Natural products CC1=CN=C(C)C(C)=C1 GFYHSKONPJXCDE-UHFFFAOYSA-N 0.000 description 1
- 125000005931 tert-butyloxycarbonyl group Chemical group [H]C([H])([H])C(OC(*)=O)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 238000002560 therapeutic procedure Methods 0.000 description 1
- 238000004809 thin layer chromatography Methods 0.000 description 1
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 1
- 210000003437 trachea Anatomy 0.000 description 1
- 230000009466 transformation Effects 0.000 description 1
- 150000003626 triacylglycerols Chemical class 0.000 description 1
- IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 1
- UAIHPMFLFVHDIN-UHFFFAOYSA-K trichloroosmium Chemical compound Cl[Os](Cl)Cl UAIHPMFLFVHDIN-UHFFFAOYSA-K 0.000 description 1
- DCXPBOFGQPCWJY-UHFFFAOYSA-N trisodium;iron(3+);hexacyanide Chemical compound [Na+].[Na+].[Na+].[Fe+3].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-] DCXPBOFGQPCWJY-UHFFFAOYSA-N 0.000 description 1
- 230000004584 weight gain Effects 0.000 description 1
- 235000019786 weight gain Nutrition 0.000 description 1
- 229910052727 yttrium Inorganic materials 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/72—Nitrogen atoms
- C07D213/73—Unsubstituted amino or imino radicals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/06—Antihyperlipidemics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/72—Nitrogen atoms
- C07D213/75—Amino or imino radicals, acylated by carboxylic or carbonic acids, or by sulfur or nitrogen analogues thereof, e.g. carbamates
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/55—Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Diabetes (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Obesity (AREA)
- Hematology (AREA)
- Emergency Medicine (AREA)
- Endocrinology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Pyridine Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
This invention relates to processes for preparing compounds of the formula (I) and to processes for preparing certain intermediates of the formula wherein R1 is nitro, amino or protected amino; R2 is H, fluoro, chloro CF3, nitro, (Cr C4)alkyl, (CrC4)alkoxy, amino or protected amino; and X1 is OH or a suitable leaving group, used in that process. The invention also relates novel to compounds of the formulae (II).
Description
Process for Substituted Pyridines
Background of the Invention
The present invention relates to certain compounds of the formula (llA) depicted below, which are useful in the synthesis of certain β-adrenergic receptor agonists having the general formula (I):
where R1 and R2 are as defined herein for the compound of formula (llA) hereinbelow and Y1, Y2 and Y3 are chemical substituents which can be attached to the atoms to which they are attached. These substituents confer β-adrenergic receptor activity and as such the compounds of formula (I) have utility as hypoglycemic and antiobesity agents. Examples of such substituents and the resultant β-adrenergic receptor agonists can be found in PCT Publication No. WO 94/29290 published December 22, 1994. The invention also relates to a process for synthesizing the compounds of formula (II) hereinbelow and to a process for synthesizing compounds of the formula (III), which are useful in the synthesis of the compounds of formula (I). The invention further relates to processes for synthesizing compounds of formula (I). The β-adrenergic receptor agonists also possess utility for increasing lean meat deposition and/or improving the lean meat to fat ratio in edible animals.
The β-adrenergic receptor agonists further possess utility in the treatment of intestinal motility disorders, depression, prostate disease, dyslipidemia, and airway inflammatory disorders such as asthma and obstructive lung disease.
The disease diabetes mellitus is characterized by metabolic defects in production and/or utilization of carbohydrates which result in the failure to maintain appropriate blood sugar levels. The result of these defects is elevated blood glucose or hyperglycemia. Research in the treatment of diabetes has centered on attempts to normalize fasting and postprandial blood glucose levels. Current treatments include administration of exogenous insulin, oral administration of drugs and dietary therapies.
AP/P/ 97/01 147
AP.00805
-2Two major forms of diabetes mellitus are recognized. Type I diabetes, or insulindependent diabetes, is the result of an absolute deficiency of insulin, the hormone which regulates carbohydrate utilization. Type II diabetes, or non-insulin dependent diabetes, often occurs with normal, or even elevated levels of insulin and appears to be the result of the inability of tissues to respond appropriately to insulin. Most of the Type II diabetics are also obese.
The β-adrenergic receptor agonists effectively lower blood glucose levels when administered orally to mammals with hyperglycemia or diabetes.
The β-adrenergic receptor agonists also reduce body weight or decrease weight 10 gam when administered to mammals. The ability of β-adrenergic receptor agonists to affect weight gain is due to activation of β-adrenergic receptors which stimulate the metabolism of adipose tissue.
β-Adrenergic receptors have been categorized into Br, β2- and B3-subtypes. Agonists of β-receptors promote the activation of adenyl cyclase. Activation of βΓ receptors invokes increases in heart rate while activation of B2-receptors induces relaxation of skeletal muscle tissue which produces a drop in blood pressure and the onset of smooth muscle tremors. Activation of B3-receptors is known to stimulate lipolysis (the breakdown of adipose tissue triglycerides to glycerol and free fatty acids) and metabolic rate (energy expenditure), and thereby promote the loss of fat mass.
Compounds that stimulate β-receptors are, therefore, useful as anti-obesity agents, and can also be used to increase the content of lean meat in edible animals. In addition, compounds which are B3-receptor agonists have hypoglycemic or anti-diabetic activity, but the mechanism of this effect is unknown.
Until recently B3-adrenergic receptors were thought to be found predominantly in adipose tissue. B3-receptors are now known to be located in such diverse tissues as the intestine (J. Clin. Invest., 91, 344 (1993)) and the brain (Eur. J. Pharm., 219,193 (1992)). Stimulation of the B3-receptor has been demonstrated to cause relaxation of smooth muscle in colon, trachea and bronchi. Life Sciences, 44(19), 1411 (1989); Br. J. Pharm., .1.12, 55 (1994); Br. J. Pharmacol., 110, 1311 (1993). For example, stimulation of β330 receptors has been found to induce relaxation of histamine-contracted guinea pig ileum,
J.Pharm.Exp.Ther., 260.1, 192 (1992).
The B3-receptor is also expressed in human prostate. Because stimulation of the B3-receptor causes relaxation of smooth muscles that have been shown to express
AP/P/ 9 7/01147
AF. ΰ ΰ 8 Ο 5
-3the B3-receptor (e.g. intestine), one skilled in the art would predict relaxation of prostate smooth muscle. Therefore, B3-agonists will be useful for the treatment or prevention of prostate disease.
Examples of β-adrenergic receptor agonists which can be synthesized using 5 the compounds of formula (III) can be found in PCT Publication No. WO 94/29290 published December 22, 1994, United States Patent Application No. 08/312,027 filed September 26, 1994, PCT Application No. PCT/IB95/00344 filed May 10, 1995 and United States Provisional Application No. 60/015,216 filed April 9, 1996, all of which are assigned to the assignee hereof.
With regard to the process of synthesizing a compound of formula (II) wherein
X is OH, defined hereinbelow, of the present invention, the chemical literature teaches that addition of osmium tetroxide to olefins, including the olefin moiety of allylic and styryl compounds, results in the addition of two OH groups to the double bond, with one OH group being added to each carbon atom constituting the double bond, (see
Advanced Organic Chemistry, March, John Wiley and Sons, NY, NY, 1985, 3rd Ed.) Two OH groups can also be added to double bonds by reacting the compound containing the double bond with (i) hydrogen peroxide and catalytic amounts of osmium tetroxide, (ii) alkaline potassium permanganate; (iii) hydrogen peroxide and formic acid; or (iv) iodine and silver benzoate. These methods all suffer from the drawback that they do not react stereospecifically with a prochiral carbon atom of the double bond to create an optically active dihydroxy compound.
U.S. Patent No. 5,019,578 discloses a process for preparing epoxy-pyridine compounds. That process involves hydroxy bromination of a 5-ethenyl pyridine derivative followed by cyclization to the epoxide and suffers from the disadvantage that the bromohydrin is prepared as a racemic mixture.
AP/P/ 9 7/01147
AP. ο ύ 8 ο 5
Summarv of the Invention
This invention provides compounds of the formula
wherein; R1 is selected from the group consisting of nitro, amino and protected amino; R2 is selected from the group consisting of H, fluoro, chloro, CF3, nitro, (C-|-C4)alkyl, (Ci-C4)alkoxy, amino and protected amino; X1 is OH or a suitable leaving group;
racemic mixtures thereof; R enantiomers thereof, wherein said R enantiomers are essentially free of their corresponding S enantiomers; and S enantiomers thereof, wherein said S enantiomers are essentially free of their corresponding R enantiomers thereof.
This invention particularly provides a compound as described in the immediately preceding paragraph wherein X1 is OH.
This invention more particularly provides a compound as described in the immediately preceding paragraph wherein said protected amino, for each occurrence, is independently selected from the group consisting of (C^Cgjalkylamino, -NR3CO(CH2)PR°, -NR3CO2R° and -NR3SO2(CH2)pR°; R3, for each occurrence, is independently H or (CrCeJalkyl; R°, for each occurrence, is independently (CiC10)alkyl, phenyl or phenyl independently substituted by one to three (C1-C4)alkyl, (0^ C4)alkoxy or halo; and p is 0, 1 or 2.
This invention still more particularly provides compounds as described in the immediately preceding paragraph wherein R2 is H.
This invention still more particularly provides compounds as described in the immediately preceding paragraph wherein R1 is amino, -NR3CO(Ci-C10)alkyl, -NR3CO2(CrC8)alkyl or -NR3CO(CH2)PR0
This invention still more particularly provides compounds as described in the immediately preceding paragraph wherein R1 is amino or -NR^OiCrC^Jalkyl.
AP/P/ 9 7/01 147
AP. ο Ο 8 ο 5
-5This invention still more particularly provides N-(5-(1,2-dihydroxyethyl)-pyridin-2yl)-acetamide. Still further, this invention provides the R enantiomer of N-(5-(1,2dihydroxyethyl)-pyridin-2-yl)-acetamide, essentially free of its corresponding S enantiomer. Still further, this invention provides the S enantiomer of N-(5-(1,25 dihydroxyethyl)-pyridin-2-yl)-acetamide, essentially free of its corresponding R enantiomer.
This invention also provides compounds of formula (llA) above wherein X1 is a leaving group, said leaving group is organosulfonyloxy and said organosuifonyioxy is methanesulfonyloxy, benzenesulfonyloxy, p-toluenesuifonyloxy, p-nitrobenzene10 sulfonyloxy or m-nitrobenzenesulfonyloxy.
i
This invention more particularly provides those compounds as described in the immediately preceding paragraph wherein said organosulfonyloxy is ptoluenesulfonyloxy.
This invention more particularly provides compounds as described in the 15 immediately preceding paragraph wherein said protected amino, for each occurrence, is independently selected from the group consisting of (Cj-CgJalkylamino, -NR3CO(CH2)PR°, -NR3CO2R° and -NR3SO2(CH2)pR°; R3, for each occurrence, is independently H or (CrC6)alkyl; R°, for each occurrence, is independently (Cr C10)alkyl, phenyl or phenyl independently substituted by one to three (C-i-C^alkyl, (Cr
C4)alkoxy or halo; and p is 0,1 or 2.
> This invention still more particularly provides compounds as described in the %·? immediately preceding paragraph wherein R2 is H.
This invention still more particularly provides compounds as described in the immediately preceding paragraph wherein R1 is amino, -NR3CO(C1-C10)alkyI,
-NR3CO2(C1-C8)alky! or -NR3CO(CH2)pR°.
This invention still more particularly provides compounds as described in the immediately preceding paragraph wherein R1 is amino or -NR3CO(C1-C10)alkyl).
This invention.still more particularly provides toIuene-4-sulfonic acid 2-(6acetylamino-pyridin-3-yl)-2-hydroxyethyl ester. Still further, this invention provides the
R enantiomer of toluene-4-sulfonic acid 2-(6-acetylamino-pyridin-3-yl)-2-hydroxyethyl ester, essentially free of its corresponding S enantiomer. Still further, this invention provides the S enantiomer of toluene-4-sulfonic acid 2-(6-acetylamino-pyridin-3-yl)-2hydroxyethyl ester, essentially free of its corresponding R enantiomer.
AP/P/ 97/01147
AP.00805
-6This invention also provides N-(5-(2-chloro-1-hydroxyethyl)-1-pyridin-2-yl)acetamide. Still further, this invention provides the R enantiomer of N-(5-(2-chioro-1hydroxyethyl)-1-pyridin-2-yl)-acetamide, essentially free of its corresponding S enantiomer. Still further, this invention provides the S enantiomer of N(5-(2-chloro-1 5 hydroxyethyl)-1-pyridiin-2-yl)-acetamide, essentially free of its corresponding R enantiomer.
This invention also provides compounds of the formula
wherein: R1 is selected from the group consisting of nitro, amino and protected amino; R2 is selected from the group consisting of H, fluoro, chloro, CF3, nitro, (Ci-C4)alkyl, (C1-C4)alkoxy, amino and protected amino; X1 is chloro or iodo; racemic mixtures thereof; R enantiomers thereof, wherein said R enantiomers are essentially free of their corresponding S enantiomers; and S enantiomers thereof, wherein said S enantiomers are essentially free of their corresponding R enantiomers thereof.
This invention particularly provides compounds as described in the immediately preceding paragraph wherein X1 is chloro and said compound is an R enantiomer, essentially free of its corresponding S enantiomer. This invention also particularly provides compounds as described in the immediately preceding paragraph wherein X1 is chloro and said compound is an S enantiomer, essentially free of its corresponding R enantiomer.
This invention also provides compounds of the formula
AP/P/ 9 7/01147
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-7wherein: R1 is selected from the group consisting of nitro, amino and protected amino; R2 is selected from the group consisting of H, fluoro, chloro, CF3, nitro, (C1-C4)alkyl, (C-i-CJalkoxy, amino and protected amino; X1 is Br; and said compound is an (R) enantiomer, essentially free of its corresponding (S) enantiomer.
This invention also provides compounds of the formula
wherein: R1 is selected from the group consisting of nitro, amino and protected amino; 10 R2 is selected from the group consisting of H, fluoro, chioro, CF3, nitro, (Ci-C4)alkyl, (C-|-C4)alkoxy, amino and protected amino; X1 is Br; and said compound is an (S) enantiomer, essentially free of its corresponding (R) enantiomer.
This invention still further provides compounds of the formuia
OH Y4
VIII
AP/P/ 9 7 I 0 1147 wherein R12 is selected from the group consisting of nitro and protected amino; R13 is selected from the group consisting of H, fluoro, chioro, CF3, nitro, (Ci-C4)alkyl, (C-i20 C4)alkoxy and protected amino; Y4 is an amine protecting group; and Y5 is
AP.00805
MM’’
wherein Q1 is oxygen, nitrogen or sulfur; Q2 is carbon or nitrogen; Q3 is hydrogen, -(CH2)n-phenyl, -(CrC10)alkyl, -(CH2)n-NG1G2, -(CH2)n-CO2G3, -(CH2)n-CO-NG1G2, -(CH2)n-OG3, -(CH2)n-SO3G3, -(CH2)n-SO2-(CrC6)alkyl,-(CH2)n-SO2NG1G2, or a heterocycle selected from the group consisting of -(CH2)n-pyridyl, -(CH2)n-pyrimidyl, -(CH2)n-pyrazinyl, -(CH2)n-isoxazolyi, -(CH2)n-oxazolyl, -(CH2)n-thiazolyl, -(CH2)n(1,2,4-oxadiazolyl), -(CK2)n-imidazolyl, -(CH2)n-triazolyl and -(CH2)n-tetrazolyl; wherein one of the ring nitrogen atoms of said -(CH2)n-imidazolyl, -(CH2)n-triazolyl and -(CH2)ntetrazolyl may optionally be substituted by (Ci-C8)alkyl optionally independently substituted with one or more halo atoms; wherein each of said heterocycies may optionally be substituted on one or more of the ring carbon atoms by one or more substituents independently selected from the group consisting of (C-,-C8)alkyl optionally independently substituted with one or more halo atoms, halo, nitro, cyano, -(CH2)n-NG1G2, -(CH2)n-CO2G3, -(CH2)n-CO-NG1G2, -(CH2)n-OG3, -(CH2)n-SO3G3, -(CH2)n-SO2-(C1-C6)alkyl and -(CH2)n-SO2NG1G2; wherein the phenyl moiety of said -(CH2)n-phenyl may optionally be substituted with one or more substituents independently selected from the group consisting of (Ci-C6)alkyl optionally independently substituted with one or more halo atoms, hydroxy, (CrC^alkoxy optionally independently substituted with one or more halo atoms, (CvCejalkylthio, fluoro, chloro, bromo, iodo, cyano, nitro, -(CH2)n-NG1G2, -(CH2)n-CO2G3, -(CH2)n-CONG1G2, -(CH2)n-OG3, -(CH2)n-SO3G3, -(CH^-SOHCrC^alkyl, -(CH2)n-SO2NG1G2; -(CH2)n-NG3-SO2-G3 and -(CH2)n-NG3-SO2-NG1G2; Q4 is -(CH2)n-CN, -(CH2)nCO2G3, -(CH2)n-SO3G3, -(CH2)n-SO2-(CrC6)alkyl, -(CH2)n-SO2NG1G2, -(CH2)nCH2OH, -(CH2)nCHO, -(CH2)n-CO-G3, -(CH2)n-CONG1G2, or a heterocycle selected from -(CH2)nthiazolyl, -(CH2)n-oxazolyl, -(CH2)n-imidazolyl, -(CH2)n-triazolyl, -(CH2)n-1,2,4oxadiazolyl, -(CH2)n-isoxazolyl, -(CH2)n-tetrazolyl and -(CH2)n-pyrazolyl; wherein one of the ring nitrogen atoms of said -(CH2)n-imidazolyl, -(CH2)n-triazolyI and -(CH2)ntetrazolyl may optionally be substituted by (CrC^alkyl optionally independently substituted with one or more halo atoms; wherein each of said heterocycies may
L U 0 / Z 6 /d/dV
AP.00805
-9optionally be substituted on one or more of the ring carbon atoms by one or more substituents independently selected from the group consisting of hydrogen, (Cr C6)alkyl optionally independently substituted with one or more halo atoms, -(CH2)nCO-NG1G2, -(CH2)n-CO2G3, halo, nitro, cyano, -(CH2)n-CO-NG1G2, -(CH2)n-OG3,
-(CH2)n-SO3G3, -(CH2)n-SO2-(Ci-C6)alkyl, or -(CH2)n-SO2NG1G2; Q5 is hydrogen or (Ci-C6)alkyl optionally independently substituted with one or more halo atoms; Q6 is a covalent bond, oxygen or sulfur; Q7 is hydrogen or (CrC6)alkyl optionally independently substituted with one or more halo atoms; Q8 and Q9 are independently a covalent bond, oxygen, sulfur, NH or N-fCrCeJalkyl; Q10 is (CH2)mOR9, (CH2)nCO2H, (CH2)nCOR11, (CH2)nSO2NR9R10, (CH2)n-NR9SO2R8, (CH2)nP(O)(OR4)(OR5), (CH2)nO-(CH2)mCO2H, (CH2)n-O-(CH2)mCOR11, (CH2)n-O-(CH2)mP(O)(OR4)(OR5), (CH2)n-O(CH2)mSO2NR9R1°, or (CH2)n-O-(CH2)m-NR9SO2R8; R4 and R5 are each independently hydrogen or (CrC^alkyl; and R6 and R7 are each independently hydrogen, halo, (Cr C6)alkyl, nitro, cyano, trifiuoromethyl, SO2R8, SO2NR9R10, NR9R10, COR11, CO2R9, (CrC6)alkoxy, NR9SO2R8, NR9COR11, NR9CO2R9 or OR9; where G1 and G2 for each occurrence are each independently hydrogen, (CrC6)alkyl optionally independently substituted with one or more halo, (C-|-C8)alkoxy(Ci-C6)alkyl or (C3-C8)cycloalkyl, or G1 and G2 together with the nitrogen to which they are attached form a saturated heterocyclic ring having from 3 to 7 carbon atoms wherein one of said carbon atoms may optionally be replaced by oxygen, nitrogen or sulfur; G3 for each occurrence is independently hydrogen or (Ci-C6)alkyl; R8 for each occurrence is independently (C-iC6)alkyl or (Ci-C6)alkoxy(Ci-C6)alkyl; R9and R10 are taken separately and, for each occurrence, are independently hydrogen, (Ci-C6)alkyl, (C3-C8)cycloalkyl, or (C-|CeJalkoxyiC-i-CeJalkyl, or R9 and R10 are taken together with the nitrogen atom to which they are attached and form a pyrrolidine, piperidine or morpholine ring wherein said pyrrolidine, piperidine or morpholine may optionally be substituted at any carbon atom by (CrC^alkyi or (CrC4)alkoxy; R11 for each occurrence is independently hydrogen, (CrC6)alkyI, (CrC6)alkoxy, NR9R10, (C3-C8)cycloalkyl, or (CrCejalkoxyfCr C6)alkyl wherein R9 and R10 are as defined above; m for each occurrence is independently an integer of 1 to 6; and n for each occurrence is independently 0 or an integer of 1 to 6; racemic mixtures thereof; R enantiomers thereof, wherein said R enantiomer is essentially free of its corresponding S enantiomer; and S enantiomers thereof, wherein said R enantiomer is essentially free of its corresponding R
AP/P/ 9 7/01 147
AP.00805
-10enantiomer; provided that: (1) when Q9 is O or S then n is not 0; (2) when Q1 is oxygen or sulfur then Q3 is absent; and (3) when Q2 is nitrogen then Q5 is absent.
This invention particularly provides those compounds described in the immediately preceding paragraph wherein Y4 is an amine protecting group selected from the group consisting of benzyl, COR14, CO2R14 and SO2R14; and R14, for each occurrence, is independently (Ci-C10)alkyl, phenyl or benzyl; wherein said phenyl and benzyl are independently optionally substituted by one to three (C-|-C4)alkyl, (C4C4)alkoxy or halo.
This invention more particularly provides those compounds described in the immediately preceding paragraph wherein Y5 is
This invention still more particularly provides those compounds described in the immediately preceding paragraph wherein R13 is H and R12 is protected amino; said protected amino is independently selected from the group consisting of (Cr C8)alkylamino, -NR3CO(CH2)PR°, -NR3CO2R° and -NR3SO2(CH2)PR°; R3 is independently H or (Ci-Cejalkyl; R° is independently (C1-Ci0)alkyl, phenyl or phenyl independently substituted by one to three (Ci-C4)alkyl, (CrC4)alkoxy or halo; and p is 0, 1 or 2.
This invention still more particularly provides those compounds described in the immediately preceding paragraph wherein said protected amino is NR3CO(CH2)PR°; R3 is H; R° is CH3; and p is 0.
This invention still more particularly provides those compounds as described in the immediately preceding paragraph wherein R4, R5, R6 and R7 are each hydrogen; Q8 is oxygen; Q9 is a covalent bond; and Q10 is (CH2)mCONR9R10.
AP/P/ 9 7/01147
AP.00805
-11This invention still more particularly provides those compounds as described in the immediately preceding paragraph wherein Y4 is t-butyloxycarbonyl; m is 1; R9 is H; and R10 is methyl.
This invention still more particularly provides those compounds as described in 5 the immediately preceding paragraph having the formula:
This invention still more particularly provides those compounds described in the immediately preceding paragraph which are R enantiomers.
This invention still more particularly provides N-methyl 4-(2-(2-(210 acetylaminopyridin-5-yl)-2-(R)-hydroxyethyl-N-fert-butyloxycarbonylamino)-ethoxy)phenylacetamide.
This invention also provides a process for preparing compounds of the formula
AP/P/ 97/01 147
VI wherein:
R1 is selected from the group consisting of nitro, amino and protected amino;
and
R2 is selected from the group consisting of H, fluoro, chloro, CF3, nitro, (Cr
C4)alkyl, (C^C^alkoxy, amino and protected amino comprising reacting a compound of the formula
AP.00805
wherein R1 and R2 are as defined above, with a catalyst comprising an osmium (VIII) oxide or an osmium salt and an auxiliary oxidizing agent in a reaction inert solvent.
This invention also provides a process as described in the immediately preceding paragraph additionally comprising reacting said compounds of formula (V) with said osmium (VIII) oxide or said osmium salt in the presence of a chiral auxiliary ligand and an auxiliary base.
This invention particularly provides a process of the immediately preceding paragraph wherein said chiral auxiliary ligand is (DHQD)2PHAL.
This invention more particularly provides a process of the immediately preceding paragraph wherein said compound of formula (VI) has an R configuration at the 1-position of the 5-ethyl group, said compound being essentially free of its corresponding S enantiomer.
This invention still more particularly provides a process of the immediately preceding paragraph wherein R1 is acetylamino and R2 is H.
This invention also particularly provides a process for preparing compounds of 20 the formula
AP/P/ 9 7/01 147
wherein: R1 is selected from the group consisting of nitro, amino and protected amino;
and R2 is selected from the group consisting of H, fluoro, chloro, CF3, nitro, (Cr
C4)alkyl, (C^C^alkoxy, amino and protected amino comprising reacting a compound of the formula
AP. Ο Ο 8 Ο 5
R'
-13,2
R1 with a catalyst comprising an osmium (VIII) oxide or an osmium salt and an auxiliary 5 oxidizing agent in the presence of a chiral auxiliary ligand and an auxiliary base in a reaction inert solvent wherein said chiral auxiliary ligand is (DHQ)2PHAL.
This invention more particularly provides a process of the immediately preceding paragraph wherein said compound of formula (VI) has an S configuration at the 1-position of the 5-ethyl group, said compound being essentially free of its corresponding R enantiomer.
This invention still more particularly provides a process of the immediately preceding paragraph wherein R1 is acetylamino and R2 is H.
This invention also provides a process for preparing a compound of the formula (I),
AP/P/ 9 7/01 147 and the racemic-enantiomeric mixtures and optical isomers of said compounds comprising:
(a) reacting a compound of the formula
AP. Ο Ο 8 Ο 5
VI with an organosulfonyl chloride and a suitable base in a reaction inert solvent to form a compound of the formula
(b) reacting said compound of formula II with a non-nucleophilic base in a reaction inert solvent to form a compound of the formula (III)
AP/P/ 97 / 0 1147
III (c) reacting said compound of formula (III) with a base and HNY2Y3 to form said compound of formula (I); wherein:
R1 is selected from the group consisting of nitro, amino and protected amino;
R2 is selected from the group consisting of H, fluoro, chloro, CF3, nitro, (C1-C4)alkyi, (CrC4)alkoxy, amino and protected amino; and
AP. ο ο 8 Ο 5
-15Υ is Br, I or trifluoromethanesulfonyloxy; and X is organosulfonyloxy;
Y1 and Y3 are H;
Y2 is
wherein:
Q1 is oxygen, nitrogen or sulfur;
Q2 is carbon or nitrogen;
Q3 is hydrogen, -(CH2)n-phenyl,.-(CrCwJalkyl, -(CH2)n-NG1G2, -(CH2)n-CO2G3, -(CH2)n-CO-NG1G2, -(CH2)n-OG3, -(CH2)n-SO3G3, -(CH2)n-SO2-(CrC6)alkyl, -(CH2)n-SO2NG1G2, or a heterocycle selected from the group consisting of -(CH2)n-pyridyl, -(CH2)n-pyrimidyl, -(CH2)n-pyrazinyl, -(CH2)n-isoxazolyl, -(CH2)n15 oxazolyl, -(CH2)n-thiazolyl, -(CH2)n-(1,2,4-oxadiazolyl), -(CH2)n-imidazoIyl, -(CH2)n-triazolyl and -(CH2)n-tetrazolyl;
wherein one of the ring nitrogen atoms of said -(CH2)n-imidazolyl, -(CH2)n-triazolyl and -(CH2)n-tetrazolyl may optionally be substituted by (Cr C8)alkyl optionally independently substituted with one or more halo atoms; 20 wherein each of said heterocydes may optionally be substituted on one or more of the ring carbon atoms by one or more substituents independently selected from the group consisting of (CrC8)alkyl optionally independently substituted with one or more halo atoms, halo, nitro, cyano, -(CH2)n-NG1G2, -(CH2)n-CO2G3, -(CH2)n-CO-NG1G2, -(CH2)n-OG3, -(CH2)n-SO3G3, -(CHz)nSO2-(CrC6)alkyl and
-(CH2)n-SO2NG1G2;
AP/P/ 97 / 0 1147
AP.00805
-16wherein the phenyl moiety of said -(CH2)n-phenyl may optionally be substituted with one or more substituents independently selected from the group consisting of (Ci-C6)alkyl optionally independently substituted with one or more halo atoms, hydroxy, (C-i-C^alkoxy optionally independently substituted with one or more halo atoms, (C1-C6)alkylthio, fluoro, chloro, bromo, iodo, cyano, nitro, -(CH2)n-NG1G2, -(CH2)n-CO2G3, -(CH2)n-CONG1G2, -(CH2)n-OG3, -(CH2)n-SO3G3, -(CHzVSOz-iCrCeJalkyl, -(CH2)nSO2NG1G2; -(CH2)n-NG3-SO2-G3 and -(CH2)n-NG3-SO2-NG1G2;
Q4 is -(CH2)n-CN, -(CH2)nCO2G3, -(CH2)n-SO3G3, -(CH^-SCMCrCeJalkyl,
-(GH2)n-SO2NG1G2, -(CH2)nCH2OH, -(CH2)n-CHO, -(CH2)n-CO-G3, -(CH2)n-CONG1G2, or a heterocyde selected from -(CH2)n-thiazolyl, -(CH2)n-oxazolyl,
-(CH2)n-imidazolyl, -(CH2)n-triazolyl, -(CH2)n-1,2,4-oxadiazolyl, -(CH2)n-isoxazolyl, (CH2)n-tetrazoiyl and -(CH2)n-pyrazolyl;
wherein one of the ring nitrogen atoms of said -(CH2)n-imidazolyl,
-(CH2)n-triazolyl and -(CH2)n-tetrazolyl may optionally be substituted by (Cr
C6)alkyl optionally independently substituted with one or more halo atoms; wherein each of said heterocydes may optionally be substituted on one or more of the ring carbon atoms by one or more substituents independently selected from the group consisting of hydrogen, (CrC6)aIkyl optionally independently substituted with one or more halo atoms, -(CH2)n-CO? NG1G2, -(CH2)n-CO2G3, halo, nitro, cyano,
-(CH2)n-CO-NG1G2, -(CH2)n-OG3, -(CH2)n-SO3G3, -(CH2)n-SO2-(C1-C6)alkyl, or -(CH2)n-SO2NG1G2;
Q5 is hydrogen or (C-,-C6)alkyl optionally independently substituted with one or more 25 halo atoms;
Q6 is a covalent bond, oxygen or sulfur;
Q7 is hydrogen or (Ci-C6)alkyl optionally independently substituted with one or more halo atoms;
Q8 and Q9 are independently a covalent bond, oxygen, sulfur, NH or NriCrC^alkyl;
Q10 is (CH2)mOR9, (CH2)nCO2H, (CH2)nCOR11, (CH2)nSO2NR9R10, (CH2)nNR9SO2R8, (CH2)nP(O)(OR4)(OR5), (CH2)n-O-(CH2)mCO2H, (CH2)n-O-(CH2)mCOR11, (CH2)n-O-(CH2)mP(O)(OR4)(OR5), (CH2)n-O-(CH2)mSO2NR9R10, or (CH2)n-O-(CH2)mNR9SO2R8;
<r
AP. Ο Ο 8 Ο 5
-17R4 and R5 are each independently hydrogen or (CrC6)alkyl; and R6 and R7 are each independently hydrogen, halo, (Cn-C6)alkyl, nitro, cyano, trifluoromethyi, SO2R8, SO2NR9R10, NR9R10, COR11, CO2R9, (CrC6)alkoxy, NR9SO2R8, NR9COR11, NR9CO2R9 or OR9;
where G1 and G2 for each occurrence are each independently hydrogen, (C·,C6)alkyl optionally independently substituted with one or more halo, (Cr C8)alkoxy(CrC6)alkyl or (C3-C8)cycloalkyl, or G1 and G2 together with the nitrogen to which they are attached form a saturated heterocyclic ring having from 3 to 7 carbon atoms wherein one of said carbon atoms may optionally be replaced by oxygen, nitrogen or sulfur;
G3 for each occurrence is independently hydrogen or (CrC^alkyl;
R8 for each occurrence is independently (C1-C6)alkyl or (Ci-C6)alkoxy(Cr C6)alkyl;
R9 and R10 for each occurrence are independently hydrogen, (C^CgJalkyl, (C315 C8)cycloalkyl, or (C-i-CJalkoxyCC-i-CJalkyl;
R11 for each occurrence is independently hydrogen, (CrC6)alkyl. (cr C6)alkoxy, NR9R10, (C3-C8)cycloalkyl, or (C-i-CJalkoxyiC-pCJalkyl wherein R9 and R10 are as defined above;
m for each occurrence is independently an integer of 1 to 6; and n for each occurrence is independently 0 or an integer of 1 to 6;
provided that:
(1) when Q9 is O or S then n is not 0;
(2) when Q1 is oxygen or sulfur then Q3 is absent; and (3) when Q2 is nitrogen then Q5 is absent.
This invention still more particularly provides a process as described in the immediately preceding paragraph wherein said organosulfonyloxy is methanesulfonyloxy, benzenesulfonyloxy, p-toluenesulfonyloxy, p-nitrobenzenesulfonyloxy or m-nitrobenzenesulfonyloxy.
This invention also provides a process for preparing compounds of the formula
AP/P/ 9 7/01147
AP. ο Ο 8 Ο 5
wherein: R1 is selected from the group consisting of nitro, amino and protected amino; R2 is selected from the group consisting of H , fluoro, chloro, CF3, nitro, (Ci-C4)alkyl, (C-,-C4)alkoxy, amino and protected amino; and X is organosulfonyloxy, comprising: reacting a compound of the formula
VI wherein R1 and R2 are as defined above, with an organosulfonyl chloride and a suitable base in a reaction inert solvent.
This invention further provides a process for preparing compounds of the formula
Px σ>
a
CL <
Y3
Ύ2 and the racemic-enantiomeric mixtures and optical isomers of said compounds comprising:
(a) reacting a compound of the formula
AP .00805
with a non-nucleophilic base in a reaction inert solvent to form a compound of the formula (III)
III (b) reacting said compound of formula (III) with a base and HNY2Y3 to form said compound of formula (I), wherein:
R1 is selected from the group consisting of nitro, amino and protected amino;
R2 is selected from the group consisting of H, fluoro, chloro, CF3, nitro, (Ci-C4)alkyl, (C-pCJalkoxy, amino and protected amino;
X is an organosulfonyloxy group;
Y1 and Y3 are H;
Y2 is
AP/P/ 9 7/01147
AP. Ο Ο 8 Ο 5
-20wherein:
Q1 is oxygen, nitrogen or sulfur;
Q2 is carbon or nitrogen;
Q3 is hydrogen, -(CH2)n-phenyl, -(C-|-Ci0)alkyl, -(CH2)n-NG1G2, -(CH2)n-CO2G3,
-(CH2)n-CO-NG1G2, -(CH2)n-OG3, -(CH2)n-SO3G3, -(CH^n-SCMCrCeJalkyl,
-(CH2)n-SO2NG1G2, or a heterocycle selected from the group consisting of -(CH2)n-pyridyl, -(CH2)n-pyrimidyl, -(CH2)n-pyrazinyl, -(CH2)n-isoxazolyl, -(CH2)noxazolyl, -(CH2)n-thiazolyl, -(CH2)n-(1,2,4-oxadiazolyl), -(CH2)n-imidazolyl, -(CH2)n-triazolyI and -(CH2)n-tetrazolyl;
wherein one of the ring nitrogen atoms of said -(CH2)n-imidazolyl,
-(CH2)n-triazolyl and -(CH2)n-tetrazolyl may optionally be substituted by (Cf C8)alkyl optionally independently substituted with one or more halo atoms; wherein each of said heterocycles may optionally be substituted on one or more of the ring carbon atoms by one or more substituents independently selected from the group consisting of (Ci-Cs)alkyl optionally independently substituted with one or more halo atoms, halo, nitro, cyano', -(CH2)n-NG1G2, -(CH2)n-CO2G3, -(CH2)n-CO-NG1G2, -(CH2)n-OG3, -(CH2)n-SO3G3, -(CH2)nSCViCpC^alkyl and
-(CH2)n-SO2NG1G2;
wherein the phenyl moiety of said -(CH2)n-phenyl may optionally be substituted with one or more substituents independently selected from the group consisting of (Ci-C6)alkyl optionally independently substituted with one or more halo atoms, hydroxy, (CrC6)alkoxy optionally independently substituted with one or more halo atoms, (C-,-C6)alkylthio, fluoro, chloro, bromo, iodo, cyano, nitro, -(CH2)n-NG1G2, -(CH2)n-CO2G3, -(CH2)n-CONG1G2, -(CH2)n-OG3, -(CH2)n-SO3G3, -(CH2)n-SO2-(CrC6)alkyl, -(CH2)nSO2NG1G2; -(CH2)n-NG3-SO2-G3 and -(CH2)n-NG3-SO2-NG1G2;
Q4 is -(CH2)n-CN, -(CH2)nCO2G3, -(CH2)n-SO3G3, -(CH2)n-SO2-(C1-C6)aikyl, -(CH2)n-SO2NG1G2, -(CH2)nCH2OH, -(CH2)n-CHO, -(CH2)n-CO-G3, -(CH2)n-CONG1G2, or a heterocycle selected from -(CH2)n-thiazolyl, -(CH2)n-oxazolyl,
-(CH2)n-imidazolyl, -(CH2)n-triazolyl, -(CH2)n-1,2,4-oxadiazolyl, -(CH2)n-isoxazolyl, (CH2)n-tetrazolyl and -(CH2)n-pyrazolyl;
wherein one of the ring nitrogen atoms of said -(CH2)n-imidazolyl,
AP/P/ 9 7/01 147
AP. ο ο 8 Ο 5
-21-(CH2)n-triazolyl and -(CH2)n-tetrazolyl may optionally be substituted by (Cr C6)alkyl optionally independently substituted with one or more halo atoms; wherein each of said heterocycles may optionally be substituted on one or more of the ring carbon atoms by one or more substituents independently selected from the group consisting of hydrogen, (C.,-C6)alkyl optionally independently substituted with one or more halo atoms, -(CH2)n-CONG1G2, -(CH2)n-CO2G3, halo, nitro, cyano,
-(CH2)n-CO-NG1G2, -(CH2)n-OG3, -(CH2)n-SO3G3, -(CH2)n-SO2-(CrC6)alkyl, or -(CH2)n-SO2NG1G2;
Q5 is hydrogen or (C1-C6)alkyl optionally independently substituted with one or more halo atoms;
Q6 is a covalent bond, oxygen or sulfur;
Q7 is hydrogen or (Ci-C6)alkyl optionally independently substituted with one or more halo atoms;
Q8 and Q9 are independently a covalent bond, oxygen, sulfur, NH or N'^-C^alkyl;
Q10 is (CH2)mOR9, (CH2)nCO2H, (CH2)nCOR11, (CH2)nSO2NR9R10, (CH2)nNR9SO2R8, (CH2)nP(O)(OR4)(OR5), (CH2)n-O-(CH2)mCO2H, (CH2)n-O-(CH2)mCOR11, (CH2)n-O-(CH2)mP(O)(OR4)(OR5), (CH2)n-O-(CH2)mSO2NR9R10, or (CH2)n-O-(CH2)mNR9SO2R8;
R4 and R5 are each independently hydrogen or (CrC6)alkyl; and
R6 and R7 are each independently hydrogen, halo, (Ci-C6)alkyl, nitro, cyano, trifluoromethyl, SO2R8, SO2NR9R10, NR9R10, COR11, CO2R9, (C.-Cgjalkoxy, NR9SO2R8, NR9COR11, NR9CO2R9 or OR9;
where G1 and G2 for each occurrence are each independently hydrogen, (Cr
C6)alkyl optionally independently substituted with one or more halo, (Cr
C8)alkoxy(CrC6)alkyl or (C3-C8)cycloalkyl, or G1 and G2 together with the nitrogen to which they are attached form a saturated heterocyclic ring having from 3 to 7 carbon atoms wherein one of said carbon atoms may optionally be replaced by oxygen, nitrogen or sulfur;
G3 for each occurrence is independently hydrogen or (Ci-C6)alkyl;
R8 for each occurrence is independently (CrC6)alkyl or (CrCeJalkoxyiCr
C6)alkyl;
AP/P/ 9 7/01147
AP. Ο Ο 8 Ο 5
-22R9 and R10 for each occurrence are independently hydrogen, (Ci-C6)alkyl, (C3C8)cycloalkyl, or (C-rC^alkoxyfCrC^alkyl;
R11 for each occurrence is independently hydrogen, (C-|-C6)alkyl, (Cr C6)alkoxy, MR9R10, (C3-C8)cycloalkyl, or (C-i-CgjalkoxyfCvCejalkyl wherein R9 and R10 are as defined above;
m for each occurrence is independently an integer of 1 to 6; and n for each occurrence is independently 0 or an integer of 1 to 6;
provided that:
(1) when Q9 is O or S then n is not 0;
(2) when Q1 is oxygen or sulfur then Q3 is absent; and (3) when Q2 is nitrogen then Q5 is absent.
This invention particularly provides a process as described in the immediately preceding paragraph wherein said organosulfonyloxy is methanesulfonyloxy, benzenesulfonyloxy, p-toluenesulfonyloxy, p-nitrobenzenesulfonyloxy or m15 nitrobenzenesulfonyloxy.
This invention still further provides a process for preparing compounds of the formula (I),
R‘
AP/P/ 9 7/01 147
and the racemic-enantiomeric mixtures and optical isomers of said compounds comprising:
(a) reacting a compound of the formula
AP. Ο Ο 8 Ο 5
VI with an organosulfonyl chloride and a suitable base in a reaction inert to form a compound of the formula
(b) reacting said compound of formula (II) with a chlorinating agent in a 10 reaction inert solvent to form a compound of the formula (VII)
AP/P/ 9 7/01 147 (c) reacting said compound of formula (VII) with a non-nucleophilic base in a 15 reaction inert to form a compound of the formula (III)
III
AP .00805
-24(d) reacting said compound of formula (III) with a base and HNY2Y3 to form said compound of formula (I); wherein:
R1 is selected from the group consisting of nitro, amino and protected amino;
R2 is selected from the group consisting of H, fluoro, chloro, CF3, nitro, (CrCJalkyl, (CrC^alkoxy, amino and protected amino; and
X is organosulfonyloxy;
Y1 and Y3 are H;
Y2 is
wherein;
Q1 is oxygen, nitrogen or sulfur;
Q2 is carbon or nitrogen;
Q3 is hydrogen, -(CH2)n-phenyl, -(CrC^Jalkyl, -(CH2)n-NG1G2, -(CH2)r,-CO2G3, -(CH2)n-CO-NG1G2, -(CH2)n-OG3, -(CH2)n-SO3G3, -(CH2)n-SO2-(CrC6)alkyl, -(CH2)n-SO2NG1G2, or a heterocycle selected from the group consisting of -(CH2)n-pyridyl, -(CH2)n-pyrimidyl, -(CH2)n-pyrazinyl, -(CH2)n-isoxazo!yl, -(CH2)n20 oxazolyl, -(CH2)n-thiazolyl, -(CH2)n-(1,2,4-oxadiazolyl), -(CH2)n-imidazolyl, -(CH2)n-triazolyl and -(CH2)n-tetrazolyl;
wherein one of the ring nitrogen atoms of said -(CH2)n-imidazolyi, -(CH2)n-triazolyl and -(CH2)n-tetrazoIyl may optionally be substituted by (Cr C8)alkyl optionally independently substituted with one or more halo atoms;
wherein each of said heterocycles may optionally be substituted on one or more of the ring carbon atoms by one or more substituents independently
AP/P/ 9 7/01 147
AP.00805
-25selected from the group consisting of (C^CgJalkyl optionally independently substituted with one or more halo atoms, halo, nitro, cyano, -(CH2)n-NG1G2, -(CH2)n-CO2G3, -(CH2)n-CO-NG1G2, -(CH2)n-OG3, -(CH2)n-SO3G3, -(CH2)nSOa-iC-i-C^alkyl and
-(CH2)n-SO2NG1G2;
wherein the phenyl moiety of said -(CH2)n-phenyl may optionally be substituted with one or more substituents independently selected from the group consisting of (CrCejalkyl optionally independently substituted with one or more halo atoms, hydroxy, (C-|-C6)alkoxy optionally independently substituted with one or more halo atoms, (C-i-Cejalkylthio, fluoro, chloro, bromo, iodo, cyano, nitro, -(CH2)n-NG1G2, -(CH2)n-CO2G3, -(CH2)n-CONG1G2, -(CH2)n-OG3, -(CH2)n-SO3G3, -(CH2)n-SO2-(CrC6)alkyl, -(CH2)nSO2NG1G2; -(CH2)n-NG3-SO2-G3 and -(CH2)n-NG3-SO2-NG1G2;
Q4 is -(CH2)n-CN, -(CH2)nCO2G3, -(CH2)n-SO3G3, -(CH2)n-SO2-(C1-C6)alkyl,
-(CH2)n-SO2NG1G2, -(CH2)nCH2OH, -(CH2)n-CHO, -(CH2)n-CO-G3, -(CH2)n-CONG1G2, or a heterocycle selected from -(CH2)n-thiazolyl, -(CH2)n-oxazolyl,
-(CH2)n-imidazolyl, -(CH2)n-triazolyl, -(CH2)n-1,2,4-oxadiazolyl, -(CH2)n-isoxazolyl, (CH2)n-tetrazolyl and -(CH2)n-pyrazolyl;
wherein one of the ring nitrogen atoms of said -(CH2)n-imidazolyl,
-(CH2)n-triazolyl and -(CH2)n-tetrazolyl may optionally be substituted by (Cp
C6)alkyl optionally independently substituted with one or more halo atoms; wherein each of said heterocycles may optionally be substituted on one or more of the ring carbon atoms by one or more substituents independently selected from the group consisting of hydrogen, (C^-C^alkyl optionally independently substituted with one or more halo atoms, -(CH2)n-CONG1G2, -(CH2)n-CO2G3, halo, nitro, cyano,
-(CH2)n-CO-NG1G2, -(CH2)n-OG3, -(CH2)n-SO3G3, -(CH2)n-SO2-(C1-C6)alkyl, or -(CH2)n-SO2NG1G2;
Q5 is hydrogen or (C-i-C6)alkyl optionally independently substituted with one or more halo atoms;
Q6 is a covalent bond, oxygen or sulfur;
Q7 is hydrogen or (C-,-C6)alkyl optionally independently substituted with one or more halo atoms;
AP/P/ 9 7/01147
AP. υ Ο 8 Ο 5
-26Q8 and Q9 are independently a covalent bond, oxygen, sulfur, NH or N-(CrC6)alkyl;
Q10 is (CH2)mOR9, (CH2)nCO2H, (CH2)nCOR11, (CH2)nSO2NR9R10, (CH2)nNR9SO2R8, (CH2)nP(O)(OR4)(OR5), (CH2)n-O-(CH2)mCO2H, (CH2)n-O-(CH2)mCOR11, (CH2)n-O-(CH2)mP(0)(OR4)(OR5), (CH2)n-O-(CH2)mSO2NR9R10, or (CH2)n-O-(CH2)m5 NR9SO2R8;
R4 and R5 are each independently hydrogen or (C-i-Cgjalkyl; and R6 and R7 are each independently hydrogen, halo, (CrC^alkyl, nitro, cyano, trifluoromethyl, SO2R8, SO2NR9R1°, NR9R10, COR11, CO2R9, (CrC6)alkoxy, NR9SO2R8, NR9COR11, NR9CO2R9 or OR9;
where G1 and G2 for each occurrence are each independently hydrogen, (Cr
C6)alkyl optionally independently substituted with one or more halo, (C·,C8)alkoxy(Ci-C6)alkyl or (C3-C8)cycloalkyl, or G1 and G2 together with the nitrogen to which they are attached form a saturated heterocyclic ring having from 3 to 7 carbon atoms wherein one of said carbon atoms may optionally be replaced by oxygen, nitrogen or sulfur;
G3 for each occurrence is independently hydrogen or (Ci-C6)alkyl;
R8 for each occurrence is independently (CrCgjalkyl or (C1-C6)alkoxy(C1C6)alkyl;
R9and R10 for each occurrence are independently hydrogen, (CrCeJalkyl, (C320 C8)cycloalkyl, or (CrCejalkoxy^rCejalkyl;
R11 for each occurrence is independently hydrogen, (CT-C^alkyl, (Cr C6)alkoxy, NR9R10, (C3-C8)cycloalkyl, or (C1-C6)alkoxy(C1-C6)alkyl wherein R9 and R10 are as defined above;
m for each occurrence is independently an integer of 1 to 6; and n for each occurrence is independently 0 or an integer of 1 to 6;
provided that:
(1) when Q9 is O or S then n is not 0;
(2) when Q1 is oxygen or sulfur then Q3 is absent; and (3) when Q2 is nitrogen then Q5 is absent.
This invention particularly provides a process as described in the immediately preceding paragraph wherein said chlorinating agent is lithium chloride and said organosulfonyloxy is selected from the group selected consisting of
AP/P/ 9 7/01 147 methanesulfonyloxy, benzenesulfonyloxy, p-toluenesuifonyloxy, p-nitrobenzenesulfonyloxy or m-nitrobenzenesulfonyloxy.
This invention still further provides a process for preparing compounds of the formula
AP.00805
-2710
Y3
Ύ2 and the racemic-enantiomeric mixtures and optical isomers of said compounds comprising:
(a) reacting a compound of the formula
47
VI
CO £
with an organosulfonyl chloride and a suitable base in a reaction inert solvent to form a compound of the formula (II),
II (b) reacting said compound of formula (II) with a non-nucleophilic base in a reaction inert solvent to form a compound of the formula (III)
AP . υϋ805
III (c) reacting said compound of formula (III) with a base and HNY2Y3 to form said compound of formula (I), wherein:
R1 is selected from the group consisting of nitro, amino and protected amino;
R2 is selected from the group consisting of H, fluoro, chloro, CF3, nitro, (CrC4)alkyl, (C-pC^alkoxy, amino and protected amino;
X is an organosulfonyloxy group;
Y1 and Y3 are H;
Y2 is
AP/P/ 9 7/01 147 wherein:
Q1 is oxygen, nitrogen or sulfur;
Q2 is carbon or nitrogen;
Q3 is hydrogen, -(CH2)n-phenyl, -(CrC^Jalkyl, -(CH2)n-NG1G2, -(CH2)n-CO2G3, -(CH2)n-CO-NG1G2, -(CH2)n-OG3, -(CH2)n-SO3G3, -(CH2)n-SO2-(C.,-C6)alkyl, -(CH2)n-SO2NG1G2, or a heterocycle selected from the group consisting of
AP.υ υ 8 o 5
-29-(CH2)n-pyridyl, -(CH2)n-pyrimidyl, -(CH2)n-pyrazinyl, -(CH2)n-isoxazolyl, -(CH2)noxazolyl, -(CH2)n-thiazolyl, -(CH2)n-(1,2,4-oxadiazolyl), -(CH2)n-imidazolyl, -(CH2)n-triazolyl and -(CH2)n-tetrazolyl;
wherein one of the ring nitrogen atoms of said -(CH2)n-imidazolyl,
-(CH2)n-triazolyl and -(CH2)n-tetrazolyl may optionally be substituted by (Cr
C8)alkyl optionally independently substituted with one or more halo atoms; wherein each of said heterocycles may optionally be substituted on one or more of the ring carbon atoms by one or more substituents independently selected from the group consisting of (Ci-C8)alkyl optionally independently substituted with one or more halo atoms, halo, nitro, cyano,-(CH2)n-NG1G2,
-(CH2)n-CO2G3, -(CH2)n-CO-NG1G2, -(CH2)n-OG3, -(CH2)n-SO3G3, -(CH2)nSO^CrCeJalkyl and
-(CH2)n-SO2NG1G2;
wherein the phenyl moiety of said -(CH2)n-phenyl may optionally be substituted with one or more substituents independently selected from the group consisting of (CrC6)alkyl optionally independently substituted with one or more halo atoms, hydroxy, (CrC6)alkoxy optionally independently substituted with one or more halo atoms, (C-i-CeJalkylthio, fluoro, chloro, bromo, iodo, cyano, nitro, -(CH2)n-NG1G2, -(CH2)n-CO2G3, -(CH2)n-CO20 NG1G2, -(CH2)n-OG3, -(CH2)n-SO3G3, -(CH2)n-SO2-(CrC6)alkyl, -(CH2)nSO2NG1G2; -(CH2)n-NG3-SO2-G3 and -(CH2)n-NG3-SO2-NG1G2;
Q4 is -(CH2)n-CN, -(CH2)nCO2G3, -(CH2)n-SO3G3, -(CH2)n-SO2-(CrC6)alkyl, -(CH2)n-SO2NG1G2, -(CH2)nCH2OH, -(CH2)n-CHO, -(CH2)n-CO-G3, -(CH2)n-CONG1G2, or a heterocycle selected from -(CH2)n-thiazolyl, -(CH2)n-oxazolyl,
-(CH2)n-imidazolyl, -(CH2)n-triazolyl, -(CH2)n-1,2,4-oxadiazolyl, -(CH2)n-isoxazolyI, (CH2)n-tetrazolyl and -(CH2)n-pyrazolyl;
wherein one of the ring nitrogen atoms of said -(CH2)n-imidazolyl, -(CH2)n-triazolyl and -(CH2)n-tetrazolyl may optionally be substituted by (Cr C6)alkyl optionally independently substituted with one or more halo atoms;
wherein each of said heterocycles may optionally be substituted on one or more of the ring carbon atoms by one or more substituents independently selected from the group consisting of hydrogen, (Ci-C6)alkyl optionally
AP/P/ 9 7/01 147
AP.00805
-30independently substituted with one or more halo atoms, -(CH2)n-CONG1G2, -(CH2)n-GO2G3, halo, nitro, cyano,
-(CH2)n-CO-NG1G2, -(CH2)n-OG3, -(CH2)n-SO3G3, -(CH^-SCMC.-C^alkyl, or -(CH2)n-SO2NG1G2;
Q5 is hydrogen or (CrCgJalkyl optionally independently substituted with one or more halo atoms;
Q6 is a covalent bond, oxygen or sulfur;
Q7 is hydrogen or (Ci-C6)alkyl optionally independently substituted with one or more halo atoms;
Q8 and Q9 are independently a covalent bond, oxygen, sulfur, NH or N-(Ci-C6)alkyl;
Q10 is (CH2)mOR9, (CH2)nCO2H, (CH2)nCOR11, (CH2)nSO2NR9R10, (CH2)nNR9SO2R8, (CH2)nP(O)(OR4)(OR5), (CH2)n-O-(CH2)mCO2H, (CH2)n-O-(CH2)mCOR11, (CH2)n-O-(CH2)mP(O)(OR4)(OR5), (CH2)n-O-(CH2)mSO2NR9R10, or (CH2)n-O-(CH2)mNR9SO2R8;
R4 and R5 are each independently hydrogen or (Ci-C6)alkyl; and
R6 and R7 are each independently hydrogen, halo, (C-,-C6)alkyl, nitro, cyano, trifluoromethyl, SO2R8, SO2NR9R10, NR9R10, COR11, CO2R9, (CrC6)alkoxy, NR9SO2R8, NR9COR11, NR9CO2R9 or OR9;
where G1 and G2 for each occurrence are each independently hydrogen, (Cr
C6)alkyl optionally independently substituted with one or more halo, (ΟΓ
C8)alkoxy(C1-C6)alkyl or (C3-C8)cycloalkyi, or G1 and G2 together with the nitrogen to which they are attached form a saturated heterocyclic ring having from 3 to 7 carbon atoms wherein one of said carbon atoms may optionally be replaced by oxygen, nitrogen or sulfur;
G3 for each occurrence is independently hydrogen or (Ci-C6)alkyl;
R8 for each occurrence is independently (C-i-C^alkyl or (C-i-C^alkoxyiC-iC6)alkyl;
R9and R10 for each occurrence are independently hydrogen, (C^CsJalkyl, (C3C8)cycloalkyl, or (C1-C6)alkoxy(C1-C6)alkyI;
R11 for each occurrence is independently hydrogen, (Ci-C6)alkyl, (Cr
C6)alkoxy, NR9R10, (C3-C8)cycloalkyl, or (Ci-C6)alkoxy(Ci-C6)alkyl wherein R9 and R10 are as defined above;
m for each occurrence is independently an integer of 1 to 6; and
AP/P/ 9 7/01147
AP.v u 8 Ο 5
-31n for each occurrence is independently 0 or an integer of 1 to 6; provided that:
(1) when Q9 is O or S then n is not 0;
(2) when Q1 is oxygen or sulfur then Q3 is absent; and (3) when Q2 is nitrogen then Q5 is absent.
This invention particularly provides a process as described in the immediately preceding paragraph wherein said organosulfonyloxy is methanesulfonyloxy, benzenesulfonyloxy, p-toluenesulfonyloxy, p-nitrobenzenesulfonyloxy or mnitrobenzenesulfonyloxy.
This invention also provides a process for preparing a compound of the formula (XIII)
XIII comprising reacting a compound of the formula (XIV)
AP/P/ 9 7/01 147
wherein:
PG is an amine protecting group; R20 is (Ci-C8)alkyl; R21 is selected from the group consisting of (C-i-O8)alkyl, COR22, CO2R22 and SO2R22; and R22 is (C-i-C8)alkyl with an aqueous acid to form said compound of formula XIII.
AP. Ο Ο 8 Ο 5
-32This invention particularly provides a process as described in the immediately preceding paragraph wherein said amine protecting group is selected from the group consisting of COR22, CO2R22 and SO2R22; and R22 is (Ci-C8)alkyf.
This invention more particularly provides a process as described in the immediately preceding paragraph wherein said compound of formula XIV is N-methyl 4-(2-(2-(2-acetylaminopyridin-5-yl)-2-(R)-hydroxyethyl-N-ie/i-butyloxycarbonylamino)ethoxy )-phenylacetamide.
This invention also provides a process for preparing a compound of the formula
comprising:
(a) reacting a compound of the formula
AP/P/ 9 7/01 147 wherein R21 is COR22 and R22 is (CrC^alkyl with a compound of the formula
wherein R20 is (C-|-C8)alkyl in a reaction inert solvent to form a compound of the formula
AP.00805
XVI (b) reacting said compound of formula (XVI) with an acid anhydride, a dicarbonate or an acid chloride to form a compound of the formula
5-¾
XIV wherein R20 and R21 are as defined above and PG is an amine protecting group ; and (c) reacting said compound of formula (XIV) with an aqueous acid to form said compound of formula (XIII).
This invention particularly provides a process as described in the immediately preceding paragraph wherein said amine protecting group is selected from the group consisting of COR22 and CO2R22; and R22 is (CrCeJalky··
This invention more particularly provides a process as described in the immediately preceding paragraph wherein said compound of formula (XVI) is reacted with a dicarbonate.
This invention still more particularly provides a process as described in the immediately preceding paragraph wherein R21 is acetyl, R20 is methyl and PG is tertbutyloxycarbonyl.
This invention is also particularly directed to any of the processes recited hereinabove wherein said compounds of formulae (II), (III) or (VI) have the (R) configuration, said compounds being essentially free of their (S) enantiomer. This invention is also particularly directed to any of the processes recited hereinabove wherein said compounds of formulae (II), (III) or (VI) have the (S) configuration, said compounds being essentially free of their (R) enantiomer.
AP/P/ 9 7/01 147
AP . Ο 6 8 Ο 5
-34Detailed Description of the Invention
A process for the manufacture of a compound of formula (I) as defined above is provided as a feature of the invention and is illustrated by the following procedure, set forth in Scheme I, in which the meanings of generic radicals are as described hereinbelow unless otherwise specified.
Scheme I
VI
AP/P/ 9 7/01 147
Processes for the manufacture of a compound of formula (III) as defined above are illustrated by the following procedures.
The compounds of formula (I) can be synthesized from compounds of formula (III) by reaction with an amine of formula HNY2Y3, with H2NY2 being the preferred amine. This reaction is typically carried out by reacting an amine of formula HNY2Y3
AP. Ο ϋ 8 Ο 5
-3510 ί
with an epoxide of formula (III) in a polar aprotic solvent such as dimethyl sulfoxide, dimethyl formamide, acetonitrile or a lower alkanol such as ethanol, 2-propanol or butanol at a temperature from about -10°C to about 125°C. Preferably the solvent is dimethyl sulfoxide and the reaction is carried out at a temperature from about 0°C to about 10°C. If compound (III) was prepared in a stereospecific manner, as when a chiral auxiliary ligand is utilized in the step preparing the compound of formula (VI), the optical purity of the product, compound (I) will be preserved.
Alternatively, to prepare the compounds of formula (I) when Y2 is H, the amine of formula H2NY3 can be pretreated with a suitable amine protecting group. It is preferred to react said amine with N-(trimethylsilyl)acetamide to form a silylated compound of the formula (CH3)3SiNHY3. This prevents the secondary amine which results as a product of the reaction from reacting with a second epoxide molecule. This reaction is typically carried out in a polar aprotic solvent such as dimethyl sulfoxide, dimethyl formamide, acetonitrile or a lower alkanol such as ethanol, 2propanol or butanol at a temperature from about -10°C to about 125°C. Preferably, the silylation is carried out at about 25°C and the reaction with the epoxide is carried out at about 60°C. After silylation is complete, the compound of formula (CH3)3SiNHY3 is reacted with the epoxide of formula (III) as described above.
It is often desirable, when performing the coupling reaction of the epoxide of formula (III) with the amine of the formula H2NY3, to react the coupled product of the formula (XI)
AP/P/ 9 7/01 147 with an organic acid anhydride, a dicarbonate or an organic acid chloride to form a compound of the formula (XII)
AP.00805
-36ΟΗ PG I I
Ν
XII wherein R1, R2 and Υ2 are as defined herein and PG is an amine protecting group.
The term “amine protecting group” includes an organic radical which is readily attached to an amine nitrogen atom and which block said nitrogen atom from reacting with reagents and substrates used in and intermediates and transition state molecules formed in subsequent chemical transformations. Said organic radical is readily removable under mild conditions. Where used herein, the phrase “mild conditions” defines conditions which are capable of removing a protecting group but which do not have any effect upon any other portions of the substrate to which said protecting group is attached. The compounds of formula (XII) are converted, by reaction with aqueous acid, to compounds of formula (I) wherein R1 is nitro or amino; R2 is H, fluoro, chloro, CF3, nitro, (Ci-C4)alkyl, (C-j-C^alkoxy and amino; and Y2 is as defined above wherein all amine and carboxyl radicals contained within Y2 are free base and free acid forms of said amine and carboxyl radicals. Said reaction with aqueous acid is carried out with an aqueous acid such as sulfuric acid, hydrochloric acid and the like at a temperature of about 25°C to about 100°C for one hour to forty-eight hours. Preferably, the aqueous acid is hydrochloric acid and the reaction temperature is
AP/P/ 9 7/01 147 maintained at about 90°C to about 100°C for about twenty-four hours.
The compounds of formula (III) may be prepared by treating a compound of formula (II) with a non-nucleophilic base. Generally, it is preferred that the nonnucleophilic base be selected from the group consisting of sodium hydroxide, potassium hydroxide, sodium hydride, potassium fert-butoxide or 1,825 diazabicyclo[5.4.0]undec-7-ene. The reaction is preferably conducted by stirring the substrate compound of formula (II) together with the appropriate non-nucleophilic base in a reaction inert solvent at a temperature of about -20 °C to about 100 °C. Where used herein, the term reaction inert solvent
AP.00805
-37refers to any solvent which does not interact with starting materials, reagents, intermediates or products in a manner which adversely affects the reaction or the yield of the desired product. Further, the term reaction inert solvent may refer to a single, dual or multiple solvent system depending upon the nature of the reaction and the solubility of the substrate and/or reagents being disclosed. With respect to this particular reaction, it is preferred that the solvent is a polar, non-hydroxylic solvent such as an ether derivative including but not limited to tetrahydrofuran, dioxane and dimethoxyethane; chlorinated hydrocarbons including but not limited to carbon tetrachloride, chloroform and methylene chloride; aromatic hydrocarbons including but not limited to benzene, toluene and xylene; dimethylformamide; dimethylsulfoxide or any mixture of these solvents. Generally the most preferred solvent is tetrahydrofuran.
When the compounds of formula (II) disclosed herein are organosulfonyloxy derivatives, said compounds may be prepared by reacting an appropriate compound of formula (VI) with an organosulfonyl chloride in the presence of a suitable base. Suitable bases which may be used io effect this transformation include the lower trialkylamines, pyridine and pyridine derivatives. Preferred bases within those groups include but are not limited to triethylamine, diisopropyiethylamine, 2,4,6-collidine and
2,6-lutidine. Pyridine is the most preferred base. Suitable organosulfonyl chlorides include methanesulfonyl chloride, p-nitrobenzenesulfonyl chloride, mnitrobenzenesulfonyl chloride, p-toluenesulfonyl chloride and benzenesulfonyl chloride. A generally preferred organosulfonyl chloride derivative is p-toluenesulfonyl chloride. The reaction is conveniently conducted by stirring the desired substrate compound of formula (VI) together with the appropriate organosulfonyl chloride in a reaction inert solvent at a temperature of about -20 °C to about 50 °C. It is preferred that the solvent is a polar solvent such as an ether derivative including but not limited to tetrahydrofuran, dioxane and dimethoxyethane; chlorinated hydrocarbons including but not limited to carbon tetrachloride, chloroform and methylene chloride; aromatic hydrocarbons including but not limited to benzene, toluene and xylene;
dimethylformamide; N-methyl-2-pyrrolidinone; dimethylacetamide; pyridine or any mixture of these solvents. Generally the most preferred solvent is pyridine. Due to the presence of chloride ion in this reaction, the reaction product may be contaminated
AP/P/ 9 7/01 147
AP. Ο Ο 8 Ο 5
-38with 2-chloro derivatives. These mixtures can be converted entirely to the 2-chloro derivatives as described below.
To prepare the compounds of formula (llA) wherein X1 is halo, the 2organosulfonyloxy derivatives of the compound of formula (II) or mixtures thereof containing 2-chloro derivatives of the formula (llA) with a halogenating agent in a reaction inert solvent. The reaction may be conducted conveniently at a temperature of from about 25°C to the reflux temperature of the solvent utilized. It is generally preferred to conduct the reaction at the reflux temperature. Haiogenating agents are compounds which are capable of transferring a halo group to an organic substrate, said substrate having a leaving group which can be displaced by said halide ion.
Preferred halogenating agents are lithium halides. A particularly preferred chlorinating agent used to prepare the compounds of formula (Vii) is lithium chloride. A preferred solvent is ethanol.
The compounds of formula (VI) disclosed herein may be prepared by reacting an appropriate compound of formula (V) with a catalyst comprised of osmium (VIII) t
oxide or an osmium salt, in the presence of an auxiliary oxidizing agent, and optionally in the presence of a chiral auxiliary ligand such as (DHQD)2PHAL or (DHQD)2PYR and an auxiliary base. When it is desirable to use a catalyst other than osmium (VIII) oxide in this reaction, the catalyst is generally selected from osmium metal, potassium osmate (VI) dihydrate and osmium (III) chloride. Generally, it is preferred to use osmium tetroxide as the catalyst when conducting this reaction. Auxiliary oxidizing agents that may be employed include but are not limited to potassium ferricyanide, sodium ferricyanide, potassium persulfate, sodium persulfate, potassium chlorate, sodium chlorate and N-methylmorphoiine-N-oxide (the latter oxidizing agent may only be used in the absence of chiral auxiliary ligands such as (DHQD)2PHAL or (DHQD)2PYR). It may also be desirable to use a mixture of auxiliary oxidizing agents to achieve optimum performance in this reaction. An especially suitable mixture of auxiliary oxidizing agents is sodium persulfate and potassium ferricyanide. Chiral auxiliary ligands that may be used, in addition to those already recited, include hydroquinidine indoiinediyl diether ((DHQD)IND), hydroquinine phthalazinediyl diether ((DHQ)2PHAL), hydroquinine pyrimindinediyl diether ((DHQ)2PYR), hydroquinine indoiinediyl diether ((DHQ)IND), hydroquinidine phenanthrinediyl diether (DHQD-PHN) and hydroquinine phenanthrinediyl diether (DHQ-PHN). The reaction is typically
AP/P/ 9 7/01 147
AP.00805
-39conducted by stirring the desired substrate compound of formula (V) together with the appropriate reagents recited above in a polar solvent at a temperature of about -10°C to about 70°C. The reaction is conveniently conducted at about 20°C. Polar solvents which are generally useful in this reaction include water, a lower alkanol, an ether or a mixture of any of these solvents. A lower alkanol is an alcohol containing from one to four carbon atoms.
The dihydroxylation reaction disclosed in the preceding paragraph may be conducted either in the presence or in the absence of a chiral auxiliary ligand. When the reaction is conducted in the absence of a chiral auxiliary ligand, the diol product is racemic. When the reaction is conducted in the presence of a chiral auxiliary ligand, the dihydroxylation reaction proceeds stereoselectively, resulting in an essentially optically pure diol product.
The compounds of formula (V) disclosed herein may be prepared by reacting a compound of formula (IV) with ethylene gas in the presence of a base, a phosphine derivative and a palladium catalyst. Suitable bases for the reaction include lower trialkylamines, sodium carbonate, potassium carbonate, sodium bicarbonate and potassium bicarbonate. Generally, triethylamine is preferred. Suitable phosphine derivatives include triarylphosphines such as triphenylphosphine, diphenyl-2pyridylphosphine and tri-orfho-tolylphosphine, with the latter being generally preferred.
When Y is iodo, the palladium catalyst may be selected from a variety of palladium salts and complexes such as but not limited to palladium metal on carbon or some other suitable solid support, allylpalladium chloride dimer, palladium (II) chloride, palladium (II) acetate, palladium (0) tetrakis(triphenylphosphine), palladium (II) bis(triphenylphosphine) chloride, palladium (0) bis(dibenzylideneacetone) and palladium (0) bis(benzonitrile). When Y is bromo or trifluoromethanesulfonyloxy, the palladium catalyst may be selected from a variety of palladium salts and complexes such as but not limited to allylpalladium chloride dimer, palladium (II) chloride, palladium (II) acetate, palladium (0) tetrakis(triphenylphosphine), palladium (II) bis(triphenylphosphine) chloride, palladium (0) bis(dibenzylideneacetone), palladium (0) bis(benzonitrile and allylpalladium chloride dimer. Palladium (II) acetate is especially preferred. The reaction is typically conducted by stirring the compound of formula (IV) together with the above recited reagents in a polar solvent at a temperature of about 20 °C to about 150 °C under an atmosphere of ethylene at a
AP/P/ 9 7/01 147
AP . ο β 8 Ο 5
-40pressure of about 1 atmosphere to about 10 atmospheres. The preferred polar solvents for use in this reaction include, but are not limited to ethers, such as tetrahydrofuran, dimethoxyethane and dioxane; lower trialkylamines, such as triethylamine, diisopropylethylamine and tributylamine; aromatic hydrocarbons, such as benzene, toluene and xylene; dimethylformamide; N-methyl-2-pyrrolidone;
acetonitrile; dimethylacetamide; or a mixture of any of these solvents. Acetonitrile is an especially preferred solvent.
wherein R1 and R2 are as defined hereinabove and Y1, Y2 and Y3 are chemical substituents which can be attached to the atoms to which they are attached are βadrenergic receptor agonists and as such have utility as hypoglycemic and antiobesity agents. Examples of such substituents and the resultant β-adrenergic receptor agonists can be found in PCT Publication No. WO 94/29290 published December 22, 1994.
Compounds of formula (XIV) can be prepared from compounds of formula (I) wherein R1 is -NHCOiCrCejalkyl; R2 and Y3 are each H and Y2 is (CH,)
2'2^
NHiC^Cgjalkyl
AP/P/ 9 7/01 147 by reacting said compound of formula (I) with an acylating agent such as an acid anhydride of the formula ((C-|-C6)alkyl-CO)2O, an acid chloride of the formula (Cr C6)alkyl-COCI or a dicarbonate of the formula ((C1-C6)alkyl-O-CO)2-O in a reaction inert solvent at a temperature of about 0°C to about 150°C for 1 to 48 hours. Suitable reaction inert solvents for this reaction include aromatic hydrocarbons including but not limited to benzene, toluene and xylene; dimethylsulfoxide; N,Ndimethylformamide; chlorinated hydrocarbons including but not limited to methylene
AP. Ο 0 8 0 5
-41chloride, chloroform and carbon tetrachloride; ether solvents such as diethyl ether, tetrahydrofuran and dioxane or any mixture of these solvents. When a dicarbonate is used as the acylating agent, it is generally preferred to use a mixture of toluene and dimethylsulfoxide as the solvent mixture. Preferably this reaction is carried out at a temperature of about 70°C to 95°C.
The compound offormula (XIII) can be prepared from the compounds of formula (XIV) by reacting said compounds offormula (XIV) with an aqueous acid such as sulfuric acid, hydrochloric acid and the like at a temperature of about 25°C to about 100°C for one hour to forty-eight hours. Preferably, the aqueous acid is hydrochloric acid and the reaction temperature is maintained at about 90°C to about 100°C for about twenty-four hours.
It will be appreciated by those skilled in the art that the compounds of formulae , (II) and (VI) contain at least one chiral center. Accordingly, those compounds may exist in, and be isolated in, optically active and racemic forms. Some compounds may exhibit polymorphism. It is to be understood that the present invention encompasses any racemic, optically active, polymorphic or stereoisomeric form, or any mixture thereof, which form possesses properties useful in the treatment of the diseases or conditions noted herein or useful as intermediates in the preparation of any compounds useful in the treatment of said diseases or conditions, it being well known in the art how to prepare optically active forms (for example, by resolution of the racemic form by recrystallization techniques, by synthesis from optically active starting materials, by chiral synthesis or by chromatographic separation using a chiral stationary phase) and how to determine efficacy for the treatment of said utilities. In general, (R)-stereochemistry is preferred at all chiral centers in the compounds disclosed in this invention.
Conventional methods and techniques of purification and separation known to those skilled in the art may be used to isolate the compounds of this invention. Such techniques include all types of chromatography, including but not limited to high performance liquid chromatography, column chromatography using common adsorbents such as silica gel, thin layer chromatography and the like; recrystallization;
and differential (i.e., liquid-liquid) extraction techniques.
As used in the specification and appendant claims the following terms have the meanings described. The terms alkyl and alkoxy include both straight and branched chain radicals, but it is to be understood that references to individual radicals such as
AP/P/ 9 7/01 147
AP.00805
-42propyl or propoxy embrace only the straight chain radical unless reference is specifically made to for example isopropyl or isopropoxy, in which case the branched chain isomer is meant
The term haio, unless otherwise indicated, includes chloro, flouro, bromo and iodo.
The terms “Ad-mix-A” and “Ad-mix-a“ are synonymous names for a reagent used in this invention and sold by Aldrich Chemical Co. The reagent contains the chiral ligand (DHQ)2PHAL, the catalyst potassium osmate (VI) dihydrate, the auxiliary oxidizing agent potassium ferricyanide and the base potassium carbonate. The reagent is used in the asymmetric dihydroxylation of olefins. The reagent is sold by Aldrich under a license from Sepracor, Inc. of Marlborough, Massachusetts, (see Aldrich catalog, 1996-97, page 444) The terms “Ad-mix-B” and “Ad-mix-β are synonymous names for a reagent used in this invention and sold by Aldrich Chemical Co. The reagent contains the chiral ligand (DHQD)2PHAL, the catalyst potassium osmate (VI) dihydrate, the auxiliary oxidizing c
agent potassium ferricyanide and the base potassium carbonate. The reagent is used in the asymmetric dihydroxylation of olefins. The reagent is sold by Aldrich under a license from Sepracor, Inc. of Marlborough, Massachusetts, (see Aldrich catalog, 1996-97, page 444)
The term “protected amino” includes an amine nitrogen atom, e.g., RNH2 or
R2NH, to which a protecting group is attached. The term “protecting group” defines an organic radical which is readily attached to and detached from said nitrogen atom, where said group is not susceptible to reaction with or degeneration by other substrates or reagents used to transform other functional groups within the molecule to which said nitrogen atom is attached or intermediates or transition state molecules formed during such reactions. Said protecting group is readily attached and removed under mild conditions. Preferred protected amino groups include (C-i-C^aikylamino, -NR3CO(CH2)PR°, -NR3CO2R° and -NR3SO2(CH2)PR0 wherein R°, R3 and p are as defined hereinabove.
The term “suitable leaving group” includes a group which may be readily displaced by a nucleophile which has a greater affinity for the positively charged carbon atom to which said leaving group is attached than said leaving group.
Preferred leaving groups are chloro and organosulfonyloxy groups. Particularly
AP/P/ 9 7/01 147
ΛΡ.Ο 0 8 0 5
-43preferred leaving groups are organosulfonyloxy groups. Particularly preferred organosulfonyloxy groups are methanesulfonyloxy, benzenesulfonyloxy, ptoluenesulfonyloxy, p-nitrobenzenesulfonyloxy or m-nitrobenzenesulfonyloxy.
The term “suitable base includes a base which, when added to the reaction 5 mixture in which said base is to operate, increases the pH of the reaction mixture or operates on the substrate to remove a proton from said substrate or otherwise render said substrate susceptible to electrophilic attack without affecting other potentially reactive functional groups in said substrate.
The expression pharmaceutically-acceptable acid addition salts is intended to include but not be limited to such salts as the hydrochloride, hydrobromide, sulfate, hydrogen sulfate, phosphate, hydrogen phosphate, dihydrogenphosphate, acetate, succinate, citrate, methanesulfonate (mesylate) and p-toluenesulfonate (tosylate) salts.
The acid addition salts of the compounds of the present invention are readily prepared by reacting the base forms of the compounds disclosed in this invention with an appropriate acid. When the salt is of a monobasic acid (e.g., the hydrochloride, the hydrobromide, the p-toluenesulfonate, the acetate) the hydrogen form of a dibasic acid (e.g., the hydrogen sulfate, the succinate) or the dihydrogen form of a tribasic acid (e.g., the dihydrogen phosphate, the citrate), at least one molar equivalent and usually a molar excess of the acid is employed. However, when such salts as the sulfate, the hemisuccinate, the hydrogen phosphate or the phosphate are desired, the appropriate and exact chemical equivalents of acid will generally be used. The free base and the acid are conveniently combined in a co-solvent from which the desired salt precipitates or can otherwise be isolated by concentration and addition of a nonsolvent or by simple addition of a non-solvent without concentration or by lyophilization of an aqueous solution of said salt.
If not commercially available, the necessary starting materials for the chemical reactions disclosed herein may be prepared by procedures which may be selected from standard organic chemical techniques found in standard organic textbook references. The techniques found therein may be applied directly to the synthesis of known starting materials described directly in that reference or may be applied by analogy to compounds having similar functionality to achieve predictable results.
In the Examples which follow, common chemical acronyms and abbreviations are used. These acronyms and abbreviations include BOC, meaning tertAP/P/ 9 7 I 0 1147
AP.00805
-44butoxycarbonyl; Cbz, meaning benzyloxycarbonyl; THF, meaning tetrahydrofuran; DMF, meaning dimethylformamide; NMP, meaning N-methyl-2-pyrrolidinone; DMAC, meaning Ν,Ν-dimethylacetamide; DME, meaning 1,2-dimethoxyethane; DMSO, meaning dimethylsulfoxide; and TFA, meaning trifluoroacetic acid. Where used, the term “lower alkyl” means 0·,-04. By analogy, the the terms lower alkoxy, lower alkanoyloxy and lower acyloxy refer to groups containing one to four carbon atoms.
The present invention is illustrated by the following Examples. However, it should be understood that the invention is not limited to the specific details of these Examples.
AP/P/ 9 7/01147
AP.00805
N-(5-Vinyl-pyridin-2-yh-acetamide. A solution of of N-(5-bromo-pyridin-2-yi)acetamide (4.30 g, 20 mmol) in acetonitrile (15 ml) and triethylamine (5.04 ml) was treated with palladium acetate (45 mg, 0.2 mmol) and tri-o-tolylphosphine (203 mg, 0.66 mmol). The mixture was placed in a pressure reactor under 50 psig of ethylene pressure and heated at 85 °C for 66 hours. The reaction mixture was cooled, vented, and partitioned between phosphate buffer (0.1 M, pH 6.6) and ethyl acetate. The aqueous phase was extracted with ethyl acetate twice more. The combined ethyl acetate extracts were washed with additional phosphate buffer, brine and dried over sodium sulfate. The extracts were filtered and evaporated to afford 2.06 g (63%) of the title product as a flaky crystalline residue. Recrystallization from ethyl acetate/cyclohexane gave colorless flakes, mp 120 -121 °C 1H NMR (CDCI3): δ =
8.55 (br, 1 H); 8.24 (d, 1 H); 8.15 (d, 1 H); 7.76 (d of d, 1H); 6.64 (d of d, 1 H); 5.73 (d,
1 H); 5.28 (d, 1 H); 2.19 (s, 3 H). MS (Cl): m/z = 163 (M+H+).
Example Two
AP/P/ 9 7/01147
N-(5-Vinyl-pyridin-2-yl)-2.2-dimethylpropionamide. A solution of N-(5-bromopyridin-220 yl)-2,2-dimethylpropionamide (5.60 g, 21.8 mmol) in acetonitrile (20 ml) and triethylamine (5.49 ml) was treated with palladium acetate (177 mg, 0.8 mmol) and trio-tolylphosphine (795 g, 2.6 mmol). The mixture was placed in a pressure reactor under 130 psig of ethylene pressure and heated at 85 °C for 18 hours. The reaction mixture was cooled, vented, diluted with ethyl acetate and filtered. The ethyl acetate solution was washed sequentially with dilute citric acid, water and brine and then dried over sodium sulfate. The dried solution was filtered and evaporated.
Chromatography of the residue on silica gel, eluting with dichloromethane/ethyl
AP.00805
-»βacetate (24:1) afforded 3.92 g (88%) of the title product as an oil. 1H NMR (CDCI3): δ = 8.21 (m, 2 H); 8.03 (br, 1 H); 7.76 (d of d, 1 H); 6.63 (d of d, 1 H); 5.71 (d, 1 H); 5.25 (d, 1 H); 1.29 (s, 9H). MS (Cl): m/z = 205 (M+H+).
Example Three
O
X
CHJD N 3 H
N-(5-Vinyl-pyridin-2-yl)-carbamic acid methyl ester. A solution of (5-bromo-pyridin-2yl)-carbamic acid methyl ester (1.68 g, 7.2 mmol) in acetonitrile (15 ml) and triethylamine (1.84 ml) was treated with palladium acetate (65 mg, 0.29 mmol) and trio-tolylphosphine (295 mg, 0.97 mmol). The mixture was placed in a pressure reactor under 130 psig of ethylene pressure and heated at 85 °C for 18 hours. The reaction mixture was cooled, vented and diluted with ethyl acetate and filtered. The ethyl acetate solution was washed sequentially with 1M aqueous citric acid, water, brine and was dried over sodium sulfate and filtered. The filtrate was evaporated. The residue was recrystallized from dichloromethane-hexane to afford 0.759 g (58%) of the title product as colorless crystals, mp 146 -148 °C. 1H NMR (CDCI3): δ = 9.04 (br, 1 H): 8.28 (d, 1 H); 7.97 (d, 1 H); 7.77 (d of d, 1 H); 6.64 (d of d, 1 H); 5.71 (d, 1 H); 5.26 (d, 1 H); 3.81 (s, 3H). MS (Cl): m/z = 179 (M+H+).
AP/P/ 97/01147 (R)-N-(5-f1.2-Dihydroxy-ethyl)-pyridin-2-yB-acetamide. A suspension of AD-Mix-B® (56.33 g) in water (200 ml) and t-butanol (200 ml) was cooled to 5 °C and N-(5-Vinylpyridin-2-yl)-acetamide (6.52 g, 40.2 mmol) was added followed by 2-propanol (400 ml). The mixture was stirred at 5 °C for 12 hours and then at 20 °C for 12 hours. The reaction mixture was then treated with sodium sulfite (60.4 g), stirred for 30 minutes and then diluted with 500 ml of 2-propanol and stirred for an additional one hour. The mixture was filtered and the alcoholic phase was separated and evaporated to
AP.00805
-47dryness. The residue was slurried in 500 ml of 2-propanol and evaporated again. The residue was dried to afford 6.35 g (80%) of the title product as colorless crystals. The crystals were recrystallized by dissolving in hot glacial acetic acid, diluting 7-fold with 2-propanol, cooling and seeding to give the title product as crystals, mp 184-185 °C. 1H NMR (dmso-d6): δ = 8.22 (d, 1 H); 7.99 (d, 1 H); 7.68 (d of d, 1 H); 4.52 (t, 1 H);
3.44 (m, 2 H); 2.07 (s, 3 H). MS (Cl): m/z = 197 (M+H+). Optical Rotation: -4.52 ° (c = 0.05, acetic acid). Analysis: Calculated for C9H12N2O3: C, 55.09%; H,6.17%; N, 14.28%. Found: C, 55.43%; H, 5.97%; N, 13.96%.
Example Six
OH
OH
0Η3γ N (R.S)-N-(5-(1.2-Dihydroxy-ethyl)-pyridin-2-yn-acetamide. A vigorously stirred mixture of potassium carbonate (25.56 g, 185 mmol), potassium ferricyanide (60.9 g, 185. mmol) and N-(vinyl-pyridin-2-yl)-acetamide (100.0 g, 61.6 mmol) in water (120 ml) and 2-propanol (120 ml) was treated with potassium osmate (VI) dihydrate (46 mg, 0.123 mmol) at 25 °C. The mixture was then stirred for one hour. The mixture was separated and the aqueous phase was extracted three times more with 120 ml portions of 2-propanol. The residue from the aqueous phase was triturated with hot 2propanol. The 2-propanol extracts were combined, concentrated and azeotropically dried with 2-propanol. The residue was triturated with ether, filtered, washed with ether and dried to afford 10.61 g (87%) of the title product as an off white solid, mp 160-162 °C. 1H NMR (dmso-d6): δ = 8.22 (d, 1 H); 7.99 (d, 1 H); 7.68 (d of d, 1 H); 4.52 (t, 1 H); 3.44 (m, 2 H); 2.07 (s, 3 H). MS (Cl): m/z = 197 (M+H+).
AP/P/ 9 7/01 147
AP . ο ο 8 Ο 5
-48Example Seven
(R)-N-(5-(1.2-(Dihydroxy-ethyl)-pyrdin-2-yl)-carbamic acid methyl ester. A suspension of AD-Mix-B® (2.80 g) in water (10 ml) and t-butanol (10 ml) was cooled to 5 °C and
N-(5-vinyl-pyridin-2-yl)-carbamic acid methyl ester (0.356 g, 2.0 mmol) was added. The mixture was stirred at 5 °C for 18 hours. The reaction mixture was then treated with sodium sulfite (3.0 g), stirred for an additional 30 minutes and then extracted three times with ethyl acetate. The ethyl acetate extracts were combined and washed with water and brine and dried and evaporated to afford 0.410 g (96%) of the title product as colorless crystals, mp 153-154 °C. 1H NMR (CDCI3): δ = 8.90 (br, 1 H); 8.09 (d, 1 H); 7.75 (d, 1 H); 7.53 (d of d, 1 H); 4.55 (m, 1 H); 3.60 (s, 3 H); 3.47 (m, 1 H); 3.41 (m, 1 H). MS (CI): m/z = 213 (M+H+).
Example Eight
OH
AP/P/ 9 7/01 147 (R)-N-(5-(1.2-Dihydroxy-ethyl)-pyrdin-2-yl)-2.2-dimethylpropionamide. A suspension of AD-Mix-B® (1.40 g) in water (5 ml) and t-butanol (5 ml) was cooled to 5 °C and N(5-vinyi-pyridin-2-yl)-2,2-dimethyipropionamide (0.204 g, 1.0 mmol) was added. The mixture was stirred at 5 °C for 18 hours. The reaction mixture was then treated with sodium sulfite (3.0 g), stirred for 30 minutes and then extracted with dichioromethane. The dichioromethane extract was washed with water and brine and then dried and evaporated to afford 0.230 g (96%) of the title product as colorless crystals, mp 105106 °C. 1H NMR (CDCI3): δ = 8.21 (br, 1 H); 8.10 (m, 2 H); 7.61 (d of d, 1 H); 4.70 (m, 1 H); 3.64 (m, 1 H); 3.57 (m, 1 H); 1.25 (s, 9 H). MS (Cl): m/z = 239 (M+H+).
-49Example Nine
ΝΟ2 (R)-4-Nitro-benzenesulfonic acid 2-(6-acetylamino-pyridin-3-yl)-2-hydroxy-ethyl ester.
A solution of (R)-(5-(1,2-dihydroxy-ethyl)-pyridin-2-yl)-acetamide (0.294, 1.5 mmol) in anhydrous DMF (3 ml) was treated with triethylamine (0.63 g, 4.5 mmol) and cooled to -40 °C. A solution of 4-nitrobenzenesulfonyl chloride (0.332 g, 1.5 mmol) in ethyl acetate (3 ml) was added dropwise. After 45 minutes at -45 °C, the mixture was stirred for one hour at 20 °C. The mixture was then diluted with ethyl acetate and washed sequentially with water, twice with pH 6.6 buffer (0.1 M phosphate), water and brine. The ethyl acetate layer was dried over sodium sulfate, filtered and evaporated. The residue was triturated with 1,2-dichloroethane to give 0.381 g (67%) of the title product as colorless crystals, mp 116-120 °C with decomposition. 1H NMR (dmso-d6): δ = 8.36 (d, 2 H); 8.16 (d, 1 H); 8.04 (d, 2 H); 7.91 (d, 1 H); 7.62 (d of d, 1 H); 5.89 (d, 1 H); 4.81 (d of d, 1 H); 4.24 (d, 2 H); 2.06 (s, 3 H). MS (Cl): m/z = 179 (M+H+-02NC6H4SO3H).
Example Ten
OSO.
CH
O
Λ
AP/P/ 97 / 0 1 1 47 (R)-Toluene-4-sulfonic acid 2-(6-acetylamino-pyridin-3-yl)-2-hydroxy-ethvl ester. A 20 slurry of (R)-N-(5-(1,2-dihydroxy-ethyl)-pyridin-2-yl)-acetamide (71.2 g, 362 mmol) in anhydrous pyridine (362 ml) was cooled to 5 °C and treated with p-toluenesulfonyl chloride (69.18 g, 362 mmol) in one portion. The reaction mixture was stirred at 5 °C for 20 minutes, then the cooling bath was removed and the mixture was stirred at ambient temperature for two hours. The mixture was then concentrated, dissolved in
30 ml of methanol, concentrated and dissolved in toluene (300 ml) and concentrated
AP. ο Ο 8 Ο 5
-50‘(iii again. The residue was treated again with methanol and toluene, then the residue was dissolved in ethyl acetate and washed sequentially with half-saturated brine, brine and dried over sodium sulfate. The filtrate was evaporated to afford 102.2 g (80%) of the title product as light buff crystals. Recrystallization from ethanol-cyclohexane afforded the title product as colorless crystals, mp 124-126 °C. 1H NMR (dmso-d6): δ = 10.5 (br, 1 H); 8.21 (d, 1 H); 7.94 (d, 1 H); 7.68 (d, 2 H); 7.51 (d of d, 1 H); 7.41 (d, 1 H); 5.87 (d, 1 H); 4.76 (d of d, 1 H); 4.05 (d, 2 H); 2.41 (s, 3 H); 2.10 (s, 3 H). MS (Cl): m/z = 351 (M+H+). Optical Rotation: -36.181 ° (c = 1.19, acetone). Analysis: Calculated for C16H18N2O5S: C, 54.85%; H, 5.18%; N, 7.99%. Found: C, 54.91%; H,
5.34%; N, 8.06%.
Example Eleven
Γ— *4“
N-(5-(2-Qxo-[1.3]dioxolan-4-yl)-pyridin-2-yl)-acetamide. A solution of (R,S)-N-(5-(1,2dihydroxy-ethyl-pyridin-2-yl)-acetamide (0.392 g, 2 mmol) and 1,1’-carbonyldiimidazole (0.648 g, 4 mmol) in DMF (3 ml) was stirred at 20 °C for six hours and then concentrated under high vacuum. The residue was treated with water and ethyl acetate. The ethyl acetate was separated and the aqueous phase was extracted three additional times with ethyl acetate. The combined ethyl acetate extracts were washed with brine, dried, filtered and concentrated. Chromatography of the residue on silica gel, eluting with dichloromethane/methanol (1:1) afforded 0.078 g (17%) of the title product as white crystals.
mp 135-139 °C. 1H NMR (dmso-d6): δ = 8.41 (d, 1 H); 8.11 (d, 1 H); 7.93 (d of d, 1 H); 5.85 (t, 1 H); 4.84 (t, 1 H); 4.47 (t, 1 H); 2.09 (s, 3 H). MS (Cl): m/z = 223 (M+H+).
O σ>
Cl <
AP. ο ο 8 Ο 5
-51Example Twelve
OH
OH (S)-N-(5-(1.2-Dihydroxy-ethyl)-pyridin-2-yl)-acetamide. A suspension of AD-Mix-a® (35 g) in water (50 ml) and 2-propanol (50 ml) was cooled to 0 °C and N-(5-Vinyl5 pyridin-2-yl)-acetamide (4.05 g, 25 mmol) was added. The mixture was stirred overnight at 20°C. The reaction mixture was then treated with sodium sulfite (37.5 g).
The 2-propanol was decanted. The residue was diluted with 2-propanol (50 ml) and refluxed and the 2-propanol was decanted. This process was repeated three times. The alcoholic portions were combined, filtered and the filtrate was concentrated to afford a yellow solid. This solid was reslurried in hot 2-propanol (20 ml) and filtered to afford 3.80 g of impure product. This was dissolved in hot ethyl acetate (6 ml). Acetonitrile (42 ml) was added. The solution was cooled to precipitate the product. The suspension was stirred overnight and filtered to afford 3.0 g (61%) of an off-white solid. 1H NMR (dmso-d6): δ = 8.22 (d, 1 H); 7.99 (d, 1 H); 7.68 (d of d, 1 H); 4.52 (t, 1
H); 3.44 (m, 2 H); 2.07 (s, 3 H). ms (Cl); m/z = 197 (M + H+).
Example Thirteen
API'PI 97/01147
CH, N N 3 H (R)-N-(5-Oxiranyl-pyridin-2-yl)-acetamide. A solution of (R)-toluene-4-sulfonic acid 220 (6-acetylamino-pyridin-3-yl)-2-hydroxy-ethyl ester (200 g, 0.57 mol) in THF (2.4 L) was cooled to -15°C and potassium t-butoxide (542 ml, 0.542 mol, 1M in THF) was added slowly at -15°C to -10°C over a two hour period. Stirring was continued at -15°C for an additional 40 minutes. The reaction mixture was filtered with the aid of Celite®.
The filtration was done through cloth precoated with Celite®. The filter cake was washed with tetrahydrofuran. The filtrate was concentrated under vacuum to afford
0 8-05
-52300 ml of an oil. The oil was diluted with 1.2 liters of hexanes which resulted in the formation of a solid. The suspension was stirred at room temperature for one hour to granulate the solid. The suspension was filtered and the filtrate was washed with hexanes to afford 80.0 g (78.8%) of the title product as a solid, mp 96-98°C. 1H NMR (CDCIg): 5 = 8.70 (br, 1 H); 8.21 (m, 2 H); 7.57 (d of d, 1 H); 3.86 (m, 1 H); 3.17 (m, 1 H); 2.83 (m, 1 H); 2.19 (s, 3 H). MS (Cl): m/z = 179 (M+H+).
Example Fourteen
(R)-N-(5-(2-Chloro-1-hydroxy-ethyl)-pyridin-2-yl)-acetamide. A mixture of (R)-N-(5-(210 chloro-1-hydroxy-ethyl)-pyridin-2-yl)-acetamide and (R)-toluene-4-sulfonic acid 2-(6acetylamino-pyridin-3-yl)-2-hydroxy-ethyl ester (86.3 g) was dissolved in 604 mi of ethanol. The solution was heated to obtain.a clear solution and then lithium chloride (10.3 g, 0.243 mol) was added. The reaction mixture was heated under reflux overnight. Additional lithium chloride (2.0 g) was added and the reaction was heated under reflux for an additional two days. The reaction mixture was cooled and concentrated in vacuum. The residue was partitioned between ethyl acetate and halfsaturated brine. The layers were separated and the ethyl acetate layer was washed once with saturated brine. The aqueous layers were combined and extracted once with ethyl acetate. The ethyl acetate layers were combined and dried with MgSO4 then concentrated to an oil. The residue was dissolved in tetrahydrofuran to obtain a hazy solution. This solution was treated with charcoal and silica gel, stirred warm for 30 minutes and filtered. The filter cake was washed with tetrahydrofuran and the solution was concentrated to a semi-solid. The semi-solid was dissolved in 500 ml of . ethyl acetate, washed with half-saturated brine, once with saturated aqueous sodium bicarbonate and once with saturated aqueous sodium chloride. The ethyl acetate layer was concentrated to afford an oil. The resulting suspension was slurried in methylene chloride (100 ml), cooled then vacuum filtered to afford 29 g of title chloride compound. 1H NMR (DMSO-d6): δ = 10.48 (brs, 1H); 8.29 (d, 1H); 8.00 (d, 1H); 7.73 (d of d, 1H); 5.88 (d, 1H); 4.76 (m, 1H); 3.72 (m, 1H); 2.06 (s, 3H).
r*.
-4· o
CL cl <c
ΑΡ.00805
-53Example Fifteen
(4-(2-(2-(6-AminoDyridin-3-yB-2-(R)-hydroxyethylammonium)-ethoxy)-phenyl)-acetate.
A mechanically stirred slurry of the title compound of Example Thirteen (50.0gm, 0.2806mol, 1.0 eq) and the title compound of Preparation Seven (99.4gm, 0.477mol, 1.7eq) in 5:1 (vol/vol)::Toluene:DMSO (375mL) was heated on a steam bath. The slurry became homogenous at about 70°C, and the temperature was maintained at 90-95°C for 3 to 16 hrs. The solution was cooled to 10-15°. This resulted in the formation of a precipitate. Di-f-butyldicarbonate (129mL, 0.561 mol, 2.0 eq) was added dropwise over a one hour period. The resulting homogenous solution was stirred at room temperature overnight. The solution was poured into a mixture of ethyl acetate (1L) and water (850 mL). After stirring for 10 min, the phases were allowed to separate, at which time a heavy red oil fell out into the aqueous layer. The aqueous layer, with oil, was removed. The organic layer was washed with water (500mL) and concentrated to an amber oil. This amber oil was taken up in 6N HCl (300mL) and heated on the steam bath overnight. The solution was cooled to room temperature, and the solids which precipitated were filtered. (These solids are the amino acid of the excess side chain which was used in the coupling with the epoxide.) The acidic solution containing the title compound was concentrated under vacuum to a semisolid. The semi-solid was treated with water and then reconcentrated (twice) to remove excess HCl. The solid was dissolved in water and brought to pH 7 with potassium hydroxide. The solid which precipitated was filtered and washed first with water and then with THF. The solids were dried on the filter funnel to a weight of 22.5 gm. The crude solid was redissolved in 30 volumes of 90 °C water and treated with decolorizing carbon. After filtration to remove the carbon, the filtrate was cooled and concentrated by evaporation of some of the water. The precipitate which formed was filtered to provide 9.5 gm of the title compound. NMR (400MHz, DMSO-c/6 + D2O): d = 7.79 (d, 1H, J=1.87), 7.34-7.32 (m, 1H), 7.11 (d, 2H, J=8.51), 6.79 (d, 2H, J=8.51),
AP/PZ 9 7/01 147
AP. ο Ο 8 Ο 5
-546.41 (d, 1Η, J=8.51), 4.54-4.51 (m, 1 Η), 4.01-3.99 (m, 2H), 3.35 (s, 2H), 2.97-2.94 (m, 2H), 2.79-2.69 (m, 2H). MS (APCI) m/z 332.2 (MH+), 314.2, 159.1, 156.9.
Preparation One
Br
N-(5-Bromo-pyridin-2-yl)-acetamide. A solution of 2-amino-5-bromopyridine (25.0 g, 144 mmol) in acetic acid (50 ml) and acetic (25.0 g, anhydride (250 ml) was heated at reflux for two hours. The reaction mixture was then cooled and poured into water (750 ml) with stirring. After one hour, the solution was adjusted to pH 10 with 50% sodium hydroxide and the precipitate was filtered, washed with water and dried to give 26.5 g (85%) of the title product as a white flaky solid, mp 175-176 °C. 1H NMR (CDCI3): δ =
8.29 (d, 1 H); 8.12 (d, 1 H); 7.96 (br, 1 H); 7.78 (d of d, 1 H); 2.19 (s, 3 H). MS (El): m/z = 214, 216 (M+, Br isotopes).
Preparation Two
Br
Me
Me
Me
AP/P/ 97/01147
N-(5-Bromo-pyridin-2-yl)-2.2-dimethylpropionamide. A solution of trimethylacetyl chloride (17.5 g, 146 mmol) in dichloromethane (25 mi) was added to a solution of 2amino-5-bromopyridine (25.0 g, 144 mmol) in dichloromethane (100 ml) and triethylamine (24 ml) dropwise with stirring at 20 °C. The reaction mixture was then stirred for 40 minutes, filtered, washed with water, dried and concentrated.
Recrystallization from hexanes afforded 20.6 g (70%) of the title product as a white flaky solid, mp 63-64 °C. 1H NMR (CDCI3): δ = 8.82 (br, 1 H); 8.30 (d, 1 H); 8.19 (m, 2 H); 1.36 (s, 3 H). MS (El): m/z = 256, 258 (M+, Br isotopes).
AP.00805
-55Preparation Three
N-f5-Bromo-Dyridin-2-yl)-carbamic acid methyl ester. A solution of 2-amino-5bromopyridine (9.46 g, 20 mmol) and Ν,Ν-diisopropylethylamine (3.10 g) in chloroform (20 ml) was added to a solution of methyl chloroformate (2.30 g, 24 mmol) in chloroform (25 ml) dropwise with stirring at 0 °C. The reaction mixture was stirred for 20 minutes, filtered and the precipitate was washed with chloroform and dried to afford
1.71 g (37%) of the title product as a white solid, mp 191-192 °C. 1H NMR (CDCI3): δ = 8.42 (d, 1 H); 8.30 (d, 1 H); 7.91 (d, 1 H); 7.77 (d of d, 1 H); 3.79 (s, 3 H). MS (El): m/z = 230, 232 (M+, Br isotopes).
Preparation Four
N-Methvl 4-hydroxyphenylacetamide. Monomethylamine (22.43 kg, 722.15 mol, 6 eq.) was added over a 7-hour period to a solution of methyl-4-hydroxyphenylacetate (20.0 kg, 120.35 mol, 1.0 eq.) in methanol (31.7 gal) and stirred overnight at room temperature. Methanol was then displaced under vacuum with ethyl acetate. The resulting slurry (ca. 20 gal) was stirred at +10°C for 1 hour, then filtered and dried under vacuum at 45°C to yield of the title compound(18.68 kg, 94% of theory), mp 124-125°C. NMR (300 MHz, cfe-DMSO): δ = 9.26 (s, 1H), 8.00-7.65 (brs, 1H), 7.21-6.90 (m, 2H), 6.86-6.55 (m, 2H), 3.26 (s, 2H), 2.75-2.45 (m, 3H).
AP/P/ 9 7/01 147
AP. υ ο 8 Ο 5
-56Preparation Five
Ο ΝΗ
ΟΗ
N-Benzyloxycarbonyl-2-aminoethanol. Benzylchloroformate (44.95 kg, 263.5 mol, 1.0 eq.) was added over a 2 hour period at room temperature to a solution of ethanolamine (16.1 kg, 263.5 mol, 1.0 eq.) in water (34 gal). After stirring for 30 minutes, this was added to a cold (5-10°C) solution of NaHCO3 (33.2 kg, 395.25 mol,
1.5 eq) in H2O (330 L) over a 30 min period and then allowed to stir at room temperature overnight. Ethyl acetate (22 gal) was added, the layers separated, and the aqueous layer extracted again with 22 gal. ethyl acetate. The combined organic extracts were concentrated under vacuum to a volume of 10 gal, and the remainder displaced with isopropyl ether. The resulting slurry was stirred and cooled to +10°C for 2 hours, then filtered. The solids were washed with isopropyl ether and vacuum dried to give the title compound(39.1 kg, 71.1%). mp 61-63°C. NMR (300 MHz, dQDMSO): δ = 7.50-7.37 (m, 5H), 7.37-7.16 (m, 1H), 5.05 (s, 2H), 4.70-4.63 (m, 1H),
3.46-3.37 (m, 2H), 3.13-3.03 (m, 2H).
Preparation Six
NHCH ‘3
AP/P/ 9 7/01 147
Methyl 4-(2-(N-benzyloxycarbonylamino)ethoxy)phenylacetamide. The title compound 20 of Preparation Four (18.68 kg, 113.14 mol, 1.0 eq.) and the title compound of
Preparation Five (33.13 kg, 169.75 mol, 1.5 eq.) were dissolved in THF (40 gal).
Triphenylphosphine (44.5 kg, 169.75 mol, 1.5 eq.) was added and the mixture cooled to -5°C. Diisopropyl azodicarboxylate (34.3 kg, 169.75 mol, 1.5 eq.) was added over an 8 hour period, and the reaction allowed to warm to room temperature overnight.
Ethyl acetate (20 gal) was added to the resulting white slurry, stirring was continued
AP . Ο ϋ 8 0 5
-57for 6 hours, and the solids filtered off and dried to yield crude title compound. (29.6 kg, 76.5% of theory, mp 131-133°C). The crude product was slurried in ethyl acetate (39.1 gal) for 3 hours at +10°C, then filtered, washed with 14 gal 10°C ethyl acetate, and vacuum dried to yield the title compound(26.1 kg, 88.2 % recovery, 67.5% overall), mp 134-136°C. NMR (300 MHz, c/6-DMSO): δ = 7.98-7.82 (m, 1H), 7.58-7.49 (m, 1H), 7.42-7.28 (m, 5H), 7.20-7.10 (d, 2H), 6.90-6.80 (d, 2H), 5.06 (s, 2H), 4.023.93 (m, 2H), 3.47-3.29 (m, 4H), 2.62-2.54 (d, 3H).
Preparation Seven
lL,i'
Methyl 4-(2-aminoethoxy)phenylacetamide. The title compound of Preparation Six (18.4 kg, 53.73 mol) and 1.84 kg 10% palladium on carbon (50% H2O wet) were suspended in 73 gal methanol under nitrogen, and the reaction vessel pressurized to 50 psig with hydrogen gas. This H2 pressure was maintained by additional charges of c
H2 until there was no further uptake of H2 (approx. 20 hours) and the reaction was complete by tic. After purging the vessel with N2, the mixture was heated to 45°C and filtered at this temperature through Celite. The solvent was displaced with toluene until a final volume of 8 gal was achieved. After cooling to +5°C. the resulting solids were filtered off, washed with cold toluene, and vacuum dried to give the title compound (9.95 kg, 88.9% of theory). NMR (300 MHz, d6-DMSO): δ = 7.99-7.57 (m,
AP/P/ 97/01 147
1H), 7.20-7.10 (d, 2H), 6.90-6.80 (d, 2H), 3.93-3.83 (m, 2H), 3.30 (s, 2H), 3.00-2.62 (m, 4H), 2.57 (d, 2H).
Claims (2)
- Having now pariicularly described .i'-.'vriLiu’.ed my/our said invention and in a »ai snaiiiicr the same is to be per lorn tedi.’V.c deviate that what J/wc claim is —.1. A compound of the formulaX1 wherein:R1 is selected from the group consisting of nitro, amino and protected amino;R2 is selected from the group consisting of H, fluoro, chloro, CF3, nitro, (Ci-C4)alkyl, (C1-C4)alkoxy, amino and protected amino;15 X1 is OH or a suitable leaving group;racemic mixtures thereof;R enantiomers thereof, wherein said R enantiomers are essentially free of their corresponding S enantiomers; andS enantiomers thereof, wherein said S enantiomers are essentially free of their 20 corresponding R enantiomers.2. A compound of claim 1 wherein X1 is OH.3. A compound of claim 2 wherein said protected amino, for each occurrence, is independently selected from the group consisting of (Ci-C8)aikylamino, -NR3CO(CH2)PR°, -NR3CO2R° and -NR3SO2(CH2)PR°;25 R3, for each occurrence, is independently H or (C-i-CgJalkyl;R°, for each occurrence, is independently (CrC10)alkyl, phenyl or phenyl independently substituted by one to three (CrC4)alkyl, (CrC4)alkoxy or halo; and p is 0, 1 or 2.4. A compound of claim 3 wherein R2 is H.'«S' cn ££ <AP.ύ υ 8 Ο 5-595. A compound of claim 4 wherein R1 is amino, -NR^CXC-i-CicOalkyl, -NR3CO2(Ci-C8)alkyl or -NR3CO(CH2)PR°.6. A compound of claim 5 wherein R1 is amino or -NR3CO(CrC10)alkyl.7. The compound of claim 6 which is N-(5-(1,2-dihydroxyethyl)-pyridin-2-yl)5 acetamide.8. The R enantiomer of the compound of claim 7, essentially free of its corresponding S enantiomer.9. The S enantiomer of the compound of claim 7, essentially free of its corresponding R enantiomer.10 10. A compound of claim 1 wherein X1 is a leaving group, said leaving group is organosulfonyloxy and said organosulfonyloxy is methanesulfonyloxy, benzenesulfonyloxy, p-toluenesulfonyloxy, p-nitrobenzenesuifonyloxy or mnitrobenzenesuifonyloxy.11. A compound of claim 10 wherein said organosulfonyloxy is p15 toluenesulfonyloxy.12. A compound of claim 11 wherein said protected amino, for each occurrence, is independently selected from the group consisting of (C-i-CsJalkyiamino, -NR3CO(CH2)PR°, -NR3CO2R° and -NR3SO2(CH2)PR°;R3, for each occurrence, is independently H or (C1-Ce)alkyl;20 R°, for each occurrence, is independently (C-j-C-icOalkyl, phenyl or phenyl independently substituted by one to three (C-|-C4)alkyl, (CrC^alkoxy or halo; and p is 0, 1 or 2.13. A compound of claim 12 wherein R2 is H.14. A compound of claim 13 wherein R1 is amino, -NR3CO(Ci-Ci0)aikyl,25 -NR^O^CrCjOalkyl or -NR3CO(CH2)pR°.15. A compound of claim 14 wherein R1 is amino or -NR3CO(C1-C10)alkyl).16. The compound of claim 15 which is toluene-4-sulfonic acid 2-(6acetylamino-pyridin-3-yl)-2-hydroxyethyl ester.17. The R enantiomer of the compound of claim 16, essentially free of its 30 corresponding S enantiomer.18. The S enantiomer of the compound of claim 16, essentially free of its corresponding R enantiomer.AP/P/ 97 / 0 1147AP. υ ο 8 Ο 5-6019. The compound of claim 15 which is N-(5-(2-chloro-1 -hydroxyethy!)-1 pyridin-2-yl)-acetamide.20. The R enantiomer of the compound of claim 19, essentially free of its corresponding S enantiomer.5 21. The S enantiomer of the compound of claim 19, essentially free of its corresponding R enantiomer.22. A compound of claim 1 wherein X1 is a leaving group selected from chloro or iodo.23. A compound of claim 22 wherein X1 is chloro and said compound is the 10 R enantiomer, essentially free of its corresponding S enantiomer.24. A compound of claim 22 wherein X1 is chloro and said compound is the S enantiomer, essentially free of its corresponding R enantiomer.25. A compound of claim 1 wherein X1 is bromo and said compound is the R enantiomer, essentially free of its corresponding S enantiomer.15 26. A compound of claim 1 wherein X1 is bromo and said compound is theS enantiomer, essentially free of its corresponding R enantiomer.27. A compound of the formulaAP/P/ 9 7/01147 wherein:R12 is selected from the group consisting of nitro and protected amino;R13 is selected from the group consisting of H, fluoro, chloro, CF3, nitro, (Cr25 C4)aikyl, (C-|-C4)alkoxy and protected amino;Y4 is an amine protecting group; and Y5 is i i(f»· wherein:AP.00805 ,4 or5 Q1 is oxygen, nitrogen or sulfur;Q2 is carbon or nitrogen;Q3 is hydrogen, -(CH2)n-phenyl, -(CrC10)alkyl, -(CH2)n-NG1G2, -(CH2)n-CO2G3, -(CH2)n-CO-NG1G2, -(CH2)n-OG3, -(CH2)n-SO3G3, -(CH2)n-SO2-(CrC6)alkyl, -(CH2)n-SO2NG1G2, or a heterocycle selected from the group consisting of ί10 -(CH2)n-pyridyl, -(CH2)n-pyrimidyl, -(CH2)n-pyrazinyl, -(CH2)n-isoxazolyl, -(CH2)noxazolyl, -(CH2)n-thiazolyl, -(CH2)n-(1,2,4-oxadiazolyl), -(CH2)n-imidazolyl, -(CH2)n-triazolyl and -(CH2)n-tetrazolyl;wherein one of the ring nitrogen atoms of said -(CH2)n-imidazolyl,-(CH2)n-triazoIyl and -(CH2)n-tetrazolyl may optionally be substituted by (Cr C8)alkyl optionally independently substituted with one or more halo atoms; wherein each of said heterocycles may optionally be substituted on one or more of the ring carbon atoms by one or more substituents independently selected from the group consisting of (CrC8)alkyl optionally independently substituted with one or more halo atoms, halo, nitro, cyano, -(CH2)n-NG1G2, -(CH2)n-CO2G3, -(CH2)n-CO-NG1G2, -(CH2)n-OG3, -(CH2)n-SO3G3, -(CH2)nSO2-(C-,-C6)alkyl andAP/P/ 9 7/01 147 wherein the phenyl moiety of said -(CH2)n-phenyl may optionally be substituted with one or more substituents independently selected from the group consisting of (CrC^alkyl optionally independently substituted with one or more halo atoms, hydroxy, (CrC6)alkoxy optionally independently-(CH2)n-SO2NG1G2;AP. Ο Ο 8 Ο 5-62substituted with one or more halo atoms, (C-j-Cgjalkylthio, fluoro, chloro, bromo, iodo, cyano, nitro, -(CH2)n-NG1G2, -(CH2)n-CO2G3, -(CH2)n-CONG1G2, -(CH2)n-OG3, -(CH2)n-SO3G3, -(CH2)n-SO2-(Ci-C6)alkyl, -(CH2)nSO2NG1G2; -(CH2)n-NG3-SO2-G3 and -(CH2)n-NG3-SO2-NG1G2;5 Q4 is -(CH2)n-CN, -(CH2)nCO2G3, -(CH2)n-SO3G3, -(CH2)„-SO2-(CrC6)alkyl,-(CH2)n-SO2NG1G2, -(CH2)nCH2OH, -(CH2)n-CHO, -(CH2)n-CO-G3, -(CH2)n-CONG1G2, or a heterocycle selected from -(CH2)n-thiazolyl, -(CH2)n-oxazolyl,-(CH2)n-imidazolyl, -(CH2)n-triazolyl, -(CH2)n-1,2,4-oxadiazolyl, -(CH2)n-isoxazolyl, (CH2)n-tetrazolyl and -(CH2)n-pyrazolyl;10 wherein one of the ring nitrogen atoms of said -(CH2)n-imidazolyl,-(CH2)n-triazolyl and -(CH2)n-tetrazolyl may optionally be substituted by (CiCsalkyl optionally independently substituted with one or more halo atoms; wherein each of said heterocycles may optionally be substituted on one or more of the ring carbon atoms by one or more substituents independently15 selected from the group consisting of hydrogen, (Ci-C6)alkyl optionally independently substituted with one or more halo atoms, -(CH2)n-CONG1G2, -(CH2)n-CO2G3, halo, nitro, cyano,-(CH2)n-CO-NG1G2, -(CH2)n-OG3, -(CH2)n-SO3G3, -(CH^-SOHC^alkyl, or -(CH2)n-SO2NG1G2;20 Q5 is hydrogen or (Ci-C6)alkyl optionally independently substituted with one or more halo atoms;T J Q6 is a covalent bond, oxygen or sulfur;Q7 is hydrogen or (CrCSalkyl optionally independently substituted with one or more halo atoms;25 Q8 and Q9 are independently a covalent bond, oxygen, sulfur, NH or N-(CrC6)alkyl; Q10 is (CH2)mOR9, (CH2)nCO2H, (CH2)nCOR11, (CH2)nSO2NR9R10, (CH2)nNR9SO2R8, (CH2)nP(O)(OR4)(OR5), (CH2)n-O-(CH2)mCO2H, (CH2)n-O-(CH2)mCOR11, (CH2)n-O-(CH2)mP(O)(OR4)(OR5), (CH2)n-O-(CH2)mSO2NR9R10, or (CH2)n-O-(CH2)mNR9SO2R8;30 R4 and R5 are each independently hydrogen or (Ci-C6)alkyl; andR6 and R7 are each independently hydrogen, halo, (Ci-C6)alkyl, nitro, cyano, trifluoromethyl, SO2R8, SO2NR9R10, NR9R10, COR11, CO2R9, (CrC6)alkoxy,NR9SO2R8, NR9COR11, NR9CO2R9 or OR9;o cnCL aAP.00805-63where G1 and G2 for each occurrence are each independently hydrogen, (CqC6)alkyl optionally independently substituted with one or more halo, (CqC8)alkoxy(Cq-C6)alkyl or (C3-C8)cycloalkyl, or G1 and G2 together with the nitrogen to which they are attached form a saturated heterocyclic ring having5 from 3 to 7 carbon atoms wherein one of said carbon atoms may optionally be replaced by oxygen, nitrogen or sulfur;G3 for each occurrence is independently hydrogen or (Ci-C6)alkyl;R8 for each occurrence is independently (C-|-C6)alkyl or (Cq-C6)alkoxy(CqC6)alkyl;10 R9 and R10 are taken separately and, for each occurrence, are independently hydrogen, (CrC6)alkyl, (C3-C8)cycloalkyl, or (Cq-C6)alkoxy(Cq-C6)alkyl, or R9 and R10 are taken together with the nitrogen atom to which they are attached and form a pyrrolidine, piperidine or morpholine ring wherein said pyrrolidine, piperidine or morpholine may optionally be substituted at any15 carbon atom by (Cq-C4)alkyl or (C1-C4)alkoxy;R11 for each occurrence is independently hydrogen, (CrC6)alkyl, (CqC6)alkoxy, NR9R10, (C3-C8)cycloalkyl, or (Cq-C6)alkoxy(Cq-C6)alkyl wherein R9 and R10 are as defined above;m for each occurrence is independently an integer of 1 to 6; and20 n for each occurrence is independently 0 or an integer of 1 to 6;. s racemic mixtures thereof;R enantiomers thereof, wherein said R enantiomer is essentially free of its corresponding S enantiomer; andS enantiomers thereof, wherein said R enantiomer is essentially free of its25 corresponding R enantiomer; provided that:(1) when Q9 is O or S then n is not 0;
- (2) when Q1 is oxygen or sulfur then Q3 is absent; and (3) when Q2 is nitrogen then Q5 is absent.30 28. A compound of claim 27 wherein Y4 is an amine protecting group selected from the group consisting of benzyl, COR14, CO2R14 and SO2R14; and R14, for each occurrence, is independently (Cq-C10)alkyl, phenyl or benzyl; wherein saidAP/P/ 97 / 0 1 1 47AP.00805-64phenyl and benzyl are independently optionally substituted by one to three (Cr C4)alkyl, (C-i-C4)alkoxy or halo.29. A compound of claim 28 wherein Y5 is30. A compound of claim 29 wherein R13 is H and R12 is protected amino; said protected amino is independently selected from the group consisting of (Cr C8)alkylamino, -NR3CO(CH2)PR°, -NR3CO2R° and -NR3SO2(CH2)PR°;R3 is independently H or (CrC6)alkyl;R° is independently (Ci-C10)alkyl, phenyl or phenyl independently substituted by one to three (CrC4)alkyl, (CrC4)alkoxy or halo; and p is 0, 1 or 2.31. A compound of claim 30 wherein said protected amino is NR3CO(CH2)pR°; R3 is H; R° is CH3; and p is 0.32. A compound of claim 31 wherein R4, R5, R6 and R7 are each hydrogen; Q8 is oxygen; Q9 is a covalent bond; and Q10 is (CH2)mCONR9R10.33. A compound of claim 32 wherein Y4 is t-butyloxycarbonyl; m is 1; R9 is H; and R10 is methyl.34. A compound of claim 33 of the formulaAP/P/ 9 7/01 14735. A compound of claim 34 having R stereochemistry.36. The compound of claim 35 which is N-methyl 4-(2-(2-(2acetyIaminopyridin-5-yl)-2-(R)-hydroxyethyl-N-tert-butyloxycarbonylamino)-ethoxy)phenylacetamide.AP.0 0 8 0 5-6537. A process for preparing a compound of the formula ν^ί.'5 VI wherein:R1 is selected from the group consisting of nitro, amino and protected amino;and10 R2 is selected from the group consisting of H, fluoro, chloro, CF3, nitro, (CrC4)alkyl, (CrC^alkoxy, amino and protected amino comprising reacting a compound of the formula lV wherein R1 and R2 are as defined above, with a catalyst comprising an osmium (VIII) oxide or an osmium salt and an auxiliary oxidizing agent in a reaction inert solvent.20 38. A process of claim 37 additionally comprising reacting said compound of formula (V) with said osmium (VIII) oxide or said osmium salt in the presence of a chiral auxiliary ligand and an auxiliary base.39. A process of claim 38 wherein said chiral auxiliary ligand is (DHQD)2PHAL.25 40. A process of claim 39 wherein said compound of formula (VI) has an R configuration at the 1-position of the 5-ethyl group, said compound being essentially free of its corresponding S enantiomer.AP/P/ 9 7/01147AP. Ο Ο 8 Ο 541.42.(DHQ)2PHAL.43.-66Α process of claim 40 wherein R1 is acetylamino and R2 is H. A process of claim 38 wherein said chiral auxiliary ligand isA process of claim 42 wherein said compound of formula (VI) has an S configuration at the 1-position of the 5-ethyl group, said compound being essentially free of its corresponding R enantiomer.44. A process of claim 43 wherein R1 is acetylamino and R2 is H.45. A process for preparing a compound of the formula (I), n:and the racemic-enantiomeric mixtures and optical isomers of said compounds comprising:(a) reacting a compound of the formulaOHAP/P/ 9 7 / 0 1 1 4720 with an organosulfonyl chloride and a suitable base in a reaction inert solvent to form a compound of the formulaVI f :‘AAP.00805 (b) reacting said compound of formula II with a non-nucleophilic base in a reaction inert solvent to form a compound of the formula (III) RX^J°IFIII (c) reacting said compound of formula (III) with a base and HNY2Y3 to form said compound of formula (I); wherein:R1 is selected from the group consisting of nitro, amino and protected amino;R2 is selected from the group consisting of H, fluoro, chloro, CF3, nitro, (Ci-C4)alkyl, (Ci-C4)alkoxy, amino and protected amino; andY is Br, I or trifluoromethanesulfonyloxy; andX is organosulfonyloxy;Y1 and Y3 are H;Y2is orAP/P/9 7 / 0 1 1 47AP. 00805 wherein:Q1 is oxygen, nitrogen or sulfur;Q2 is carbon or nitrogen;5 Q3 is hydrogen, -(CH2)n-phenyl, -(CrC10)alkyl, -(CH2)n-NG1G2, -(CH2)n-CO2G3, -(CH2)n-CO-NG1G2, -(CH2)n-OG3, -(CH2)n-SO3G3, -(CH^-SO^CrC^alkyl, -(CH2)n-SO2NG1G2, or a heterocycle selected from the group consisting of -(CH2)n-pyridyl, -(CH2)n-pyrimidyl, -(CH2)n-pyrazinyl, -(CH2)rv-isoxazolyl, -(CH2)noxazolyl, -(CH2)n-thiazolyl, -(CH2)n-(1,2,4-oxadiazolyl), -(CH2)n-imidazolyl,10 -(CH2)n-triazolyl and -(CH2)n-tetrazolyl;wherein one of the ring nitrogen atoms of said -(CH2)n-imidazolyl, -(CH2)n-triazolyl and -(CH2)n-tetrazolyl may optionally be substituted by (C-|C8)alkyl optionally independently substituted with one or more halo atoms; wherein each of said heterocycles may optionally be substituted on one or15 more of the ring carbon atoms by one or more substituents independently selected from the group consisting of (C^C^alkyl optionally independently substituted with one or more halo atoms, halo, nitro, cyano, -(CH2)n-NG1G2, -(CH2)n-CO2G3, -(CH2)n-CO-NG1G2, -(CH2)n-OG3, -(CH2)n-SO3G3, -(CH2)nSO2-(C1-C6)alkyl and20 -(CH2)n-SO2NG1G2;wherein the phenyl moiety of said -(CH2)n-phenyl may optionally be substituted with one or more substituents independently selected from the group consisting of (CrC^alkyl optionally independently substituted with one or more halo atoms, hydroxy, (CrC6)alkoxy optionally independently25 substituted with one or more halo atoms, (C5-C6)alkylthio, fluoro, chloro, bromo, iodo, cyano, nitro, -(CH2)n-NG1G2, -(CH2)n-CO2G3, -(CH2)n-CONG1G2, -(CH2)n-OG3, -(CH2)n-SO3G3, -(CH^-SCMCrCeOalkyl, -(CH2)nSO2NG1G2; -(CH2)n-NG3-SO2-G3 and -(CH2)n-NG3-SO2-NG1G2;Q4 is -(CH2)n-CN, -(CH2)nCO2G3, -(CH2)n-SO3G3, -(CH2)n-SO2-(CrC6)alkyl,AP/P/ 9 7/01 147AP.00805-69-(CH2)n-SO2NG1G2, -(CH2)nCH2OH, -(CH2)n-CHO, -(CH2)n-CO-G3, -(CH2)n-CONG1G2, or a heterocyde selected from -(CH2)n-thiazolyl, -(CH2)n-oxazolyl,-(CH2)n-imidazolyI, -(CH2)n-triazolyl, -(CH2)n-1,2,4-oxadiazolyl, -(CH2)n-isoxazolyl, (CH2)n-tetrazolyl and -(CH2)n-pyrazolyl;5 wherein one of the ring nitrogen atoms of said -(CH2)n-imidazolyl,-(CH2)n-triazolyi and -(CH2)n-tetrazolyl may optionally be substituted by (Cr C6)alkyl optionally independently substituted with one or more halo atoms; wherein each of said heterocydes may optionally be substituted on one or more of the ring carbon atoms by one or more substituents independently10 selected from the group consisting of hydrogen, (C-t-C^alkyl optionally independently substituted with one or more halo atoms, -(CHz)n-CONG1G2, -(CH2)n-CO2G3, haio, nitro, cyano,-(CH2)n-CO-NG1G2, -(CH2)n-OG3, -(CH2)n-SO3G3, -(CH^-SOriCrC^alkyl, or -(CH2)n-SO2NG1G2;15 Q5 is hydrogen or (C-|-C6)alkyl optionally independently substituted with one or more halo atoms;Q6 is a covalent bond, oxygen or sulfur;Q7 is hydrogen or (CrC^alkyl optionally independently substituted with one or more halo atoms;20 Q8 and Q9 are independently a covalent bond, oxygen, sulfur, NH or N-iCrCeJaikyi;Q10 is (CH2)mOR9, (CH2)nCO2H, (CH2)nCOR11, (CH2)nSO2NR9R10, (CH2)nNR9SO2R8, (CH2)nP(O)(OR4)(OR5), (CH2)n-O-(CH2)mCO2H, (CH2)n-O-(CH2)mCOR11, (CH2)n-O-(CH2)mP(O)(OR4)(OR5), (CH2)n-O-(CH2)mSO2NR9R10, or (CH2)n-O-(CH2)mNR9SO2R8;25 R4 and R5 are each independently hydrogen or (Cr^aikyl; andR6 and R7 are each independently hydrogen, halo, (CrC^alkyl, nitro, cyano, trifluoromethyl, SO2R8, SO2NR9R10, NR9R1°, COR11, CO2R9, (CrC6)alkoxy, NR9SO2R8, NR9COR11, NR9CO2R9 or OR9;where G1 and G2 for each occurrence are each independently hydrogen, (C-i30 C6)alkyl optionally independently substituted with one or more halo, (CrCsialkoxyCCrCeJalkyl or (C3-C8)cycloalkyl, or G1 and G2 together with the nitrogen to which they are attached form a saturated heterocyclic ring havingAP/P/ 9 7/01147AP.U 0 8 0 5-7010 from 3 to 7 carbon atoms wherein one of said carbon atoms may optionally be replaced by oxygen, nitrogen or sulfur;G3 for each occurrence is independently hydrogen or (CrCgJalkyl;R8 for each occurrence is independently (C-|-C6)alkyl or (C-i-C^alkoxy^C6)alkyl;R9 and R10 for each occurrence are independently hydrogen, (Ci-C6)alkyl, (C3C8)cycloalkyl, or (C-,-C6)alkoxy(C-,-C6)alkyI;R11 for each occurrence is independently hydrogen, (CrC^alkyl, (C-iC8)alkoxy, NR9R10, (C3-C8)cycloalkyl, or (Ci-C6)alkoxy(Ci-C6)alkyl wherein R9 and R10 are as defined above;m for each occurrence is independently an integer of 1 to 6; and n for each occurrence is independently 0 or an integer of 1 to 6;provided that:(1) when Q9 is O or S then n is not 0;(2) when Q1 is oxygen or sulfur then Q3 is absent; and (3) when Q2 is nitrogen then Q5 is absent.46. A process of claim 45 wherein said organosulfonyloxy is methanesulfonyloxy, benzenesulfonyloxy, p-toluenesulfonyloxy, p-nitrobenzenesulfonyloxy or m-nitrobenzenesulfonyloxy.47. A process for preparing a compound of formulaAP/P/9 7 / 0 1147 wherein: R1 is selected from the group consisting of nitro, amino and protected amino; R2 is selected from the group consisting of H , fluoro, chloro, CF3, nitro, (C^C^alkyl, (C-|-C4)alkoxy, amino and protected amino; and X is organosulfonyloxy, comprising: reacting a compound of the formulaAP. Ο Ο 8 Ο 5VI wherein R1 and R2 are as defined above, with an organosulfonyl chloride and a suitable base in a reaction inert solvent.48. A process for preparing a compound of the formulaY3Ύ2 and the racemic-enantiomeric mixtures and optical isomers of said compounds comprising:(a) reacting a compound of the formulaAP/P/ 9 7/01147 with a non-nucleophilic base in a reaction inert solvent to form a compound of the formula (III)AP. Ο Ο 8 Ο 5III (b) reacting said compound of formula (III) with a base and HNY2Y3 to form said compound of formula (I), wherein:R1 is selected from the group consisting of nitro, amino and protected amino;R2 is selected from the group consisting of H, fluoro, chloro, CF3, nitro, (C-|-C4)alkyl, (C-|-C4)alkoxy, amino and protected amino;X is an organosulfonyloxy group;Y1 and Y3 are H;Y2 isAP/P/ 9 7/01147 wherein:Q1 is oxygen, nitrogen or sulfur;Q2 is carbon or nitrogen;Q3 is hydrogen, -(CH2)n-phenyl, -(CrC10)alkyl, -(CH2)n-NG1G2, -(CH2)n-CO2G3, -(CH2)n-CO-NG1G2, -(CH2)n-OG3, -(CH2)n-SO3G3, -(CH2)n-SO2-(CrC6)alkyl, -(CH2)n-SO2NG1G2, or a heterocycle selected from the group consisting of -(CH2)n-pyridyl, -(CH2)n-pyrimidyl, -(CH2)n-pyrazinyl, -(CH2)n-isoxazolyl, -(CH2)noxazolyl, -(CH2)n-thiazolyi, -(CH2)n-(1,2,4-oxadiazolyl), -(CH2)n-imidazolyl,AP.0 Ο 8 Ο 5-73-(CH2)n-triazolyl and -(CH2)n-tetrazolyl;wherein one of the ring nitrogen atoms of said -(CH2)n-imidazolyi, -(CH2)n-triazolyl and -(CH2)n-tetrazolyl may optionally be substituted by (Cr C8)alkyl optionally independently substituted with one or more halo atoms;5 wherein each of said heterocydes may optionally be substituted on one or more of the ring carbon atoms by one or more substituents independently selected from the group consisting of (C-j-CeJaikyl optionally independently substituted with one or more halo atoms, halo, nitro, cyano, -(CH2)n-NG1G2, -(CH2)n-CO2G3, -(CH2)n-CO-NG1G2, -(CH2)n-OG3, -(CH2)n-SO3G3, -(CH2)n10 SOHCrCeJalkyl and-(CH2)n-SO2NG1G2;wherein the phenyl moiety of said -(CH2)n-phenyl may optionally be substituted with one or more substituents independently selected from the group consisting of (C1-C6)alkyl optionally independently substituted with15 one or more halo atoms, hydroxy, (CrCeJalkoxy optionally independently substituted with one or more halo atoms, (Ci-Ce)alkylthio, fluoro, chloro, bromo, iodo, cyano, nitro, -(CH2)n-NG1G2, -(CH2)n-CO2G3, -(CH2)n-CONG1G2, -(CH2)n-OG3, -(CH2)n-SO3G3, -(CH^-SOz-iCrC^alkyl, -(CH2)nSO2NG1G2; -(CH2)n-NG3-SO2-G3 and -(CH2)n-NG3-SO2-NG1G2;20 Q4 is -(CH2)n-CN, -(CH2)nCO2G3, -(CH2)n-SO3G3, -(CH^n-SOHCrC^alkyl,-(CH2)n-SO2NG1G2, -(CH2)nCH2OH, -(CH2)n-CHO, -(CH2)n-CO-G3, -(CH2)n-CONG1G2, or a heterocycle selected from -(CH2)n-thiazolyl, -(CH2)n-oxazolyl,-(CH2)n-imidazolyl, -(CH2)n-triazolyl, -(CH2)n-1,2,4-oxadiazolyl, -(CH2)n-isoxazolyl, (CH2)n-tetrazolyl and -(CH2)n-pyrazolyl;25 wherein one of the ring nitrogen atoms of said -(CH2)n-imidazolyl,-(CH2)n-triazolyl and -(CH2)n-tetrazolyl may optionally be substituted by (Cr C6)alkyl optionally independently substituted with one or more halo atoms; wherein each of said heterocydes may optionally be substituted on one or more of the ring carbon atoms by one or more substituents independently30 selected from the group consisting of hydrogen, (Ci-C6)aikyl optionally independently substituted with one or more halo atoms, -(CH2)n-CONG1G2, -(CH2)n-CO2G3, halo, nitro, cyano,AP/P/ 97/01147AP.00805
-(CH2)n-CO-NG1G2, -(CH2)n-OG3, -(CH2)n-SO3G3, -(CH^-SCM^-C^alkyl, or -(CH2)n-SO2NG1G2; Q5 is hydrogen or (C^-C^alkyl optionally independently substituted with one or more halo atoms; 5 Q6 is a covalent bond, oxygen or sulfur; Q7 is hydrogen or (C-i-Cejaikyl optionally independently substituted with one or more halo atoms; Q8 and Q9 are independently a covalent bond, oxygen, sulfur, NH or N-(C-j-C6)alkyl; Q10 is (CH2)mOR9, (CH2)nCO2H, (CH2)nCOR11, (CH2)nSO2NR9R10, (CH2)n- 10 NR9SO2R8, (CH2)nP(O)(OR4)(OR5), (CH2)n-O-(CH2)mCO2H, (CH2)n-O-(CH2)mCOR11, (CH2)n-O-(CH2)mP(O)(OR4)(OR5), (CH2)n-O-(CH2)mSO2NR9R10, or (CH2)n-O-(CH2)mNR9SO2R8; R4 and R5 are each independently hydrogen or (Ci-C6)alkyl; and R6 and R7 are each independently hydrogen, halo, (Ci-C6)alkyl, nitro, cyano, 15 trifiuoromethyl, SO2R8, SO2NR9R10, NR9R10, COR11, CO2R9, (C^Cejalkoxy, NR9SO2R8, NR9COR11, NR9CO2R9 or OR9; where G1 and G2 for each occurrence are each independently hydrogen, (C-iC6)alkyl optionally independently substituted with one or more halo, (C-|CgjalkoxytC-i-CeJalkyl or (C3-C8)cycloalkyl, or G1 and G2 together with the 20 nitrogen to which they are attached form a saturated heterocyclic ring having from 3 to 7 carbon atoms wherein one of said carbon atoms may optionally be replaced by oxygen, nitrogen or sulfur; G3 for each occurrence is independently hydrogen or (CrC6)alkyl; R8 for each occurrence is independently (CrC6)alkyl or (Ci-C6)alkoxy(C-|- 25 C6)alkyl; R9 and R10 for each occurrence are independently hydrogen, (CrCejalkyl, (C3C8)cycloalkyl, or (Ci-C6)aikoxy(C-|-C6)alkyl; R11 for each occurrence is independently hydrogen, (Ci-C6)alkyl, (C·)C6)alkoxy, NR9R10, (C3-C8)cycloalkyl, or (C-i-CgjalkoxyCC-i-Cejalkyl wherein R9 30 and R10 are as defined above; m for each occurrence is independently an integer of 1 to 6; and n for each occurrence is independently 0 or an integer of 1 to 6; provided that: AP/P/ 9 7/01 147AP.00805-75(1) when Q9 is O or S then n is not 0;(2) when Q1 is oxygen or sulfur then Q3 is absent; and (3) when Q2 is nitrogen then Q5 is absent.49. A process of claim 48 wherein said organosulfonyloxy is methanesulfonyloxy, benzenesulfonyloxy, p-toluenesulfonyloxy, p-nitrobenzenesulfonyloxy or m-nitrobenzenesulfonyloxy.50. A process for preparing a compound of the formula (I), .'1N ^Y2 and the racemic-enantiomeric mixtures and optical isomers of said compounds comprising:(a) reacting a compound of the formulaOHOHAP/P/ 9 7/01 147VI with an organosulfonyl chloride and a suitable base in a reaction inert to form a compound of the formulaAP.00805-76(b) reacting said compound of formula (ll) with a chlorinating agent in a reaction inert solvent to form a compound of the formula (VII) (c) reacting said compound of formula (VII) with a non-nucleophilic base in a reaction inert to form a compound of the formula (III) *«·III (d) reacting said compound of formula (III) with a base and HNY2Y3 to form said compound of formula (I); wherein:R1 is selected from the group consisting of nitro, amino and protected amino;R2 is selected from the group consisting of H, fluoro, chloro, CF3, nitro, (C-j-C^alkyl, (Ci-C4)alkoxy, amino and protected amino; andX is organosulfonyloxy;Y1 and Y3 are H;Y2 is o>aClΑΡ. 008ο5 wherein:Q1 is oxygen, nitrogen or sulfur;Q2 is carbon or nitrogen;5 Q3 is hydrogen, -(CH2)n-phenyl, -(CrC10)alkyl, -(CH2)n-NG1G2, -(CH2)n-CO2G3, -(CH2)n-CO-NG1G2, -(CH2)n-OG3, -(CH2)n-SO3G3, -(CH2)n-SO2-(C1-C6)alkyl, -(CH2)n-SO2NG1G2, or a heterocycle selected from the group consisting of -(CH2)n-pyridyl, -(CH2)n-pyrimidyl, -(CH2)n-pyrazinyl, -(CH2)n-isoxazolyl, -(CH2)noxazolyl, -(CH2)n-thiazolyl, -(CH2)n-(1,2,4-oxadiazolyl), -(CH2)n-imidazolyl,10 -(CH2)n-triazolyl and -(CH2)n-tetrazolyl;wherein one of the ring nitrogen atoms of said -(CH2)n-imidazolyl, -(CH2)n-triazolyl and -(CH2)n-tetrazoIyl may optionally be substituted by (Cr C8)alkyl optionally independently substituted with one or more halo atoms; wherein each of said heterocycles may optionally be substituted on one or15 more of the ring carbon atoms by one or more substituents independently selected from the group consisting of (C-,-Ce)aIkyl optionally independently substituted with one or more halo atoms, halo, nitro, cyano, -(CH2)n-NG1G2, -(CH2)n-CO2G3, -(CH2)n-CO-NG1G2, -(CH2)n-OG3, -(CH2)n-SO3G3, -(CH2)nSO2-(CrC6)alkyi and20 -(CH2)n-SO2NG1G2;wherein the phenyl moiety of said -(CH2)n-phenyl may optionally be substituted with one or more substituents independently selected from the group consisting of (C^-C^alkyl optionally independently substituted with one or more halo atoms, hydroxy, (CrC6)alkoxy optionally independently25 substituted with one or more halo atoms, (CpC^alkylthio, fluoro, chloro, bromo, iodo, cyano, nitro, -(CH2)n-NG1G2, -(CH2)n-CO2G3, -(CH2)n-CONG1G2, -(CH2)n-OG3, -(CH2)n-SO3G3, -(CH^-SOHCvC^alkyl, -(CH2)nSO2NG1G2; -(CH2)n-NG3-SO2-G3 and -(CH2)n-NG3-SO2-NG1G2;Q4 is -(CH2)n-CN, -(CH2)nCO2G3, -(CH2)n-SO3G3, -(CH2)n-SO2-(CrC6)alkyl,AP/P/ 9 7/01 147AP.00805-78-(CH2)n-SO2NG1G2, -(CH2)nCH2OH, -(CH2)n-CHO, -(CH2)n-CO-G3, -(CH2)n-CONG1G2, or a heterocycle selected from -(CH2)n-thiazolyl, -(CH2)n-oxazolyl,-(CH2)n-imidazolyl, -(CH2)n-triazolyl, -(CH2)n-1,2,4-oxadiazolyl, -(CH2)n-isoxazolyl, (CH2)n-tetrazolyl and -(CH2)n-pyrazolyl;5 wherein one of the ring nitrogen atoms of said -(CH2)n-imidazolyl,-(CH2)n-triazolyi and -(CH2)n-tetrazolyl may optionally be substituted by (C-r C6)alkyl optionally independently substituted with one or more halo atoms; wherein each of said heterocycles may optionally be substituted on one or more of the ring carbon atoms by one or more substituents independently10 selected from the group consisting of hydrogen, (Cq-CeJalkyi optionally independently substituted with one or more halo atoms, -(CH2)n-CONG1G2, -(CH2)n-CO2G3, halo, nitro, cyano,-(CH2)n-CO-NG1G2, -(CH2)n-OG3, -(CH2)n-SO3G3, -(CH^-SOHCrC^alkyl, or -(CH2)n-SO2NG1G2;15 Q5 is hydrogen or (C5-C6)alkyl optionally independently substituted with one or more halo atoms;Q6 is a covalent bond, oxygen or sulfur;Q7 is hydrogen or (C-i-C^alkyl optionally independently substituted with one or more halo atoms;20 Q8 and Q9 are independently a covalent bond, oxygen, sulfur, NH or N-(CrC6)alkyl; Q10 is (CH2)mOR9, (CH2)nCO2H, (CH2)nCOR11, (CH2)nSO2NR9R10, (CH2)nNR9SO2R8, (CH2)nP(O)(OR4)(OR5), (CH2)n-O-(CH2)mCO2H, (CH2)n-O-(CH2)mCOR11, (CH2)n-O-(CH2)mP(O)(OR4)(OR5), (CH2)n-O-(CH2)mSO2NR9R10, or (CH2)n-O-(CH2)mNR9SO2R8;25 R4 and R5 are each independently hydrogen or (CrC6)alkyl; andR6 and R7 are each independently hydrogen, halo, (Ci-C6)alkyl, nitro, cyano, trifluoromethyl, SO2R8, SO2NR9R10, NR9R10, COR11, CO2R9, (C-,-C6)alkoxy, NR9SO2R8, NR9COR11, NR9CO2R9 or OR9;where G1 and G2 for each occurrence are each independently hydrogen, (C-|30 C6)alkyl optionally independently substituted with one or more halo, (CrCgjalkoxyiC-i-Cejalkyl or (C3-C8)cycloalkyl, or G1 and G2 together with the nitrogen to which they are attached form a saturated heterocyclic ring havingAP/P/ 9 7/01 147AP.00805-79(1) when Q9 15 (2) when Q1 (3) when Q2 51.from 3 to 7 carbon atoms wherein one of said carbon atoms may optionally be replaced by oxygen, nitrogen or sulfur;G3 for each occurrence is independently hydrogen or (C-i-CeJalkyl;R8 for each occurrence is independently (C^CeJalkyl or (C-pCeJalkoxyiC-i5 C6)alkyl;R9 and R10 for each occurrence are independently hydrogen, (CrC6)alkyl, (C3C8)cycloalkyl, or (C1-C6)alkoxy(C1-C6)alkyl;R11 for each occurrence is independently hydrogen, (C-|-C6)alkyl, (Cr C6)alkoxy, NR9R10, (C3-C8)cycloalkyl, or (C1-C6)alkoxy(C1-C6)alkyl wherein R9 10 and R10 are as defined above;m for each occurrence is independently an integer of 1 to 6; and n for each occurrence is independently 0 or an integer of 1 to 6; provided that:s O or S then n is not 0; s oxygen or sulfur then Q3 is absent; and s nitrogen then Q5 is absent.A process of claim 50 wherein said chlorinating agent is lithium chloride and said organosulfonyloxy is selected from the group selected consisting of methanesulfonyloxy, benzenesulfonyloxy, p-toluenesulfonyloxy, p-nitrobenzene20 sulfonyloxy or m-nitrobenzenesulfonyloxy.52. A process of claim 48 wherein prior to said step (a), said compound of formula (II) is prepared by reacting a compound of the formulaOHAP/P/ 9 7/01 147VI with an organosulfonyl chloride and a suitable base in a reaction inert solvent.AP.00805-8053. A process of claim 52 wherein said organosulfonyloxy is methanesulfonyloxy, benzenesulfonyloxy, p-toluenesulfonyloxy, p-nitrobenzenesulfonyloxy or m-nitrobenzenesulfonyloxy.54. A process for preparing a compound of the formula (XIII)XIII10 comprising reacting a compound of the formula (XIV) 'vi*'XIVAP/P/ 9 7/0114715 wherein:PG is an amine protecting group;R15 * * * * 20 is (CrC8)alkyl;R21 is selected from the group consisting of (CrCeJalkyl, COR22 * * 25, CO2R22 andSO2R22; and20 R22 is (C-|-C8)alkyl with an aqueous acid.55. A process of claim 54 wherein said amine protecting group is selected from the group consisting of COR22, CO2R22 and SO2R22; and R22 is (Ci-C8)alkyl.56. A process of claim 55 wherein said compound of formula XIV is Nmethyl 4-(2-(2-(2-acetylaminopyridin-5-yl)-2-(R)-hydroxyethyl-N-ferf25 butyloxycarbonylamino)-ethoxy)-phenylacetamide.AP.008055 comprising:(a) reacting a compound of the formula3£ ·*XV wherein R21 is COR22 and R22 is (C-i-Cgjalkyl with a compound of the formulaNHR20 r*.*α· oj*».OlCL <wherein R20 is (C-,-C8)alkyl in a reaction inert solvent to form a compound of the formulaXVIAP. ύ Ο 8 Ο 5-82(b) reacting said compound of formula (XVI) with an acid anhydride, a dicarbonate or an acid chloride to form a compound of the formulaXIV5 wherein R20 and R21 are as defined above and PG is an amine protecting group ; and (c) reacting said compound of formula (XIV) with an aqueous acid to form said compound of formula (XIII).58. A process of claim 57 wherein said amine protecting group is selected from the group consisting of COR22 and CO2R22; and R22 is (CrCgJalkyl.10 59. A process of claim 58 wherein said compound of formula (XVI) is reacted with a dicarbonate.60. A process of claim 59 wherein R21 is acetyl, R20 is methyl and PG is tert-butyl oxycarbony I.
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US6455734B1 (en) * | 2000-08-09 | 2002-09-24 | Magnesium Diagnostics, Inc. | Antagonists of the magnesium binding defect as therapeutic agents and methods for treatment of abnormal physiological states |
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JPWO2003033468A1 (en) * | 2001-10-17 | 2005-02-03 | 株式会社カネカ | Method for producing (S) -α-halomethylpyridine methanol derivative |
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AU2003209527A1 (en) * | 2002-02-27 | 2003-09-09 | Pfizer Products Inc. | Crystal forms of (r)-2-(2-(4-oxazol-4-yl-phenoxy)-ethylamino)-1-pyridin-3-yl-ethanol |
US6864268B2 (en) | 2002-02-27 | 2005-03-08 | Pfizer Inc. | β3 adrenergic receptor agonists |
EP1424079A1 (en) * | 2002-11-27 | 2004-06-02 | Boehringer Ingelheim International GmbH | Combination of a beta-3-receptor agonist and of a reuptake inhibitor of serotonin and/or norepinephrine |
EP1660484B1 (en) | 2003-05-09 | 2008-08-27 | F. Hoffmann-La Roche Ag | Methyl indoles and methyl pyrrolopyridines as alpha-1 adrenergic agonists |
US7977359B2 (en) | 2005-11-04 | 2011-07-12 | Amira Pharmaceuticals, Inc. | 5-lipdxygenase-activating protein (FLAP) inhibitors |
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US8399666B2 (en) | 2005-11-04 | 2013-03-19 | Panmira Pharmaceuticals, Llc | 5-lipoxygenase-activating protein (FLAP) inhibitors |
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