CN1735600A - 3-phenyl-cinnoline homologue and antitumor agent containing the same - Google Patents
3-phenyl-cinnoline homologue and antitumor agent containing the same Download PDFInfo
- Publication number
- CN1735600A CN1735600A CN 200380108285 CN200380108285A CN1735600A CN 1735600 A CN1735600 A CN 1735600A CN 200380108285 CN200380108285 CN 200380108285 CN 200380108285 A CN200380108285 A CN 200380108285A CN 1735600 A CN1735600 A CN 1735600A
- Authority
- CN
- China
- Prior art keywords
- trifluoromethyl
- cinnolines
- methyl
- phenyl
- hydrogen atom
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 239000002246 antineoplastic agent Substances 0.000 title claims abstract description 38
- AJUMVVYEUXGKQU-UHFFFAOYSA-N 3-phenylcinnoline Chemical compound C1=CC=CC=C1C1=CC2=CC=CC=C2N=N1 AJUMVVYEUXGKQU-UHFFFAOYSA-N 0.000 title claims abstract description 33
- 150000003839 salts Chemical class 0.000 claims abstract description 24
- 150000001875 compounds Chemical class 0.000 claims description 171
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 94
- 150000001854 cinnolines Chemical class 0.000 claims description 77
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 64
- 125000000217 alkyl group Chemical group 0.000 claims description 63
- 239000001301 oxygen Substances 0.000 claims description 60
- 229910052760 oxygen Inorganic materials 0.000 claims description 60
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 53
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 37
- 229910052721 tungsten Inorganic materials 0.000 claims description 36
- 125000003545 alkoxy group Chemical group 0.000 claims description 35
- 229940034982 antineoplastic agent Drugs 0.000 claims description 35
- 125000005843 halogen group Chemical group 0.000 claims description 20
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 19
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 19
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 16
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 16
- 230000035479 physiological effects, processes and functions Effects 0.000 claims description 16
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 15
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 14
- 239000004480 active ingredient Substances 0.000 claims description 12
- 125000003368 amide group Chemical group 0.000 claims description 12
- 229910052799 carbon Inorganic materials 0.000 claims description 12
- 125000002252 acyl group Chemical group 0.000 claims description 11
- 125000004432 carbon atom Chemical group C* 0.000 claims description 11
- 125000003282 alkyl amino group Chemical group 0.000 claims description 8
- 125000000539 amino acid group Chemical group 0.000 claims description 8
- 150000001350 alkyl halides Chemical class 0.000 claims description 7
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 7
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 6
- XMVJITFPVVRMHC-UHFFFAOYSA-N roxarsone Chemical group OC1=CC=C([As](O)(O)=O)C=C1[N+]([O-])=O XMVJITFPVVRMHC-UHFFFAOYSA-N 0.000 claims description 6
- 125000003630 glycyl group Chemical group [H]N([H])C([H])([H])C(*)=O 0.000 claims description 5
- 230000035407 negative regulation of cell proliferation Effects 0.000 claims description 5
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 5
- 125000001980 alanyl group Chemical group 0.000 claims description 3
- 125000002114 valyl group Chemical group 0.000 claims description 3
- 239000000470 constituent Substances 0.000 abstract description 3
- 239000000824 cytostatic agent Substances 0.000 abstract 1
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 108
- 238000000034 method Methods 0.000 description 76
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 58
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 57
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical class OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 55
- 101100043731 Caenorhabditis elegans syx-3 gene Proteins 0.000 description 38
- 101100535673 Drosophila melanogaster Syn gene Proteins 0.000 description 38
- 101100368134 Mus musculus Syn1 gene Proteins 0.000 description 38
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 36
- -1 for example Chemical group 0.000 description 33
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 29
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 27
- 238000006243 chemical reaction Methods 0.000 description 27
- 239000012295 chemical reaction liquid Substances 0.000 description 27
- HJSLFCCWAKVHIW-UHFFFAOYSA-N cyclohexane-1,3-dione Chemical class O=C1CCCC(=O)C1 HJSLFCCWAKVHIW-UHFFFAOYSA-N 0.000 description 27
- 230000002829 reductive effect Effects 0.000 description 27
- 239000000243 solution Substances 0.000 description 26
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 25
- CZDYPVPMEAXLPK-UHFFFAOYSA-N tetramethylsilane Chemical compound C[Si](C)(C)C CZDYPVPMEAXLPK-UHFFFAOYSA-N 0.000 description 24
- 238000005160 1H NMR spectroscopy Methods 0.000 description 23
- 239000007787 solid Substances 0.000 description 19
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 18
- 239000012044 organic layer Substances 0.000 description 17
- 238000010898 silica gel chromatography Methods 0.000 description 17
- 238000002360 preparation method Methods 0.000 description 16
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 15
- 239000003960 organic solvent Substances 0.000 description 15
- 239000000203 mixture Chemical group 0.000 description 14
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 14
- 238000003756 stirring Methods 0.000 description 13
- PMZBHPUNQNKBOA-UHFFFAOYSA-N 5-methylbenzene-1,3-dicarboxylic acid Chemical compound CC1=CC(C(O)=O)=CC(C(O)=O)=C1 PMZBHPUNQNKBOA-UHFFFAOYSA-N 0.000 description 12
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 12
- TZIYNLSEBAYCBZ-UHFFFAOYSA-N 2-bromo-1-[3-(trifluoromethyl)phenyl]ethanone Chemical compound FC(F)(F)C1=CC=CC(C(=O)CBr)=C1 TZIYNLSEBAYCBZ-UHFFFAOYSA-N 0.000 description 11
- 206010028980 Neoplasm Diseases 0.000 description 11
- 239000012153 distilled water Substances 0.000 description 11
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 10
- 230000000259 anti-tumor effect Effects 0.000 description 10
- 238000012545 processing Methods 0.000 description 10
- 238000010992 reflux Methods 0.000 description 10
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
- 239000007864 aqueous solution Substances 0.000 description 9
- 239000002585 base Substances 0.000 description 9
- 238000001035 drying Methods 0.000 description 9
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 9
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 8
- 230000000694 effects Effects 0.000 description 8
- 206010006187 Breast cancer Diseases 0.000 description 7
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 7
- 239000003513 alkali Substances 0.000 description 7
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 7
- 239000007788 liquid Substances 0.000 description 7
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Substances [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 7
- 235000015320 potassium carbonate Nutrition 0.000 description 7
- 210000004881 tumor cell Anatomy 0.000 description 7
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
- 208000026310 Breast neoplasm Diseases 0.000 description 6
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 6
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 6
- WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 6
- 229960003328 benzoyl peroxide Drugs 0.000 description 6
- 201000011510 cancer Diseases 0.000 description 6
- 210000004027 cell Anatomy 0.000 description 6
- 238000003810 ethyl acetate extraction Methods 0.000 description 6
- 239000000284 extract Substances 0.000 description 6
- 230000002194 synthesizing effect Effects 0.000 description 6
- 238000011282 treatment Methods 0.000 description 6
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 5
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 5
- BIVUUOPIAYRCAP-UHFFFAOYSA-N aminoazanium;chloride Chemical compound Cl.NN BIVUUOPIAYRCAP-UHFFFAOYSA-N 0.000 description 5
- 125000001246 bromo group Chemical group Br* 0.000 description 5
- 239000012141 concentrate Substances 0.000 description 5
- 235000008504 concentrate Nutrition 0.000 description 5
- 125000003754 ethoxycarbonyl group Chemical group C(=O)(OCC)* 0.000 description 5
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 5
- 238000001914 filtration Methods 0.000 description 5
- QSSXJPIWXQTSIX-UHFFFAOYSA-N 1-bromo-2-methylbenzene Chemical compound CC1=CC=CC=C1Br QSSXJPIWXQTSIX-UHFFFAOYSA-N 0.000 description 4
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical group [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 4
- KWOLFJPFCHCOCG-UHFFFAOYSA-N Acetophenone Chemical compound CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 description 4
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 4
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 4
- 239000002253 acid Substances 0.000 description 4
- 238000002512 chemotherapy Methods 0.000 description 4
- 238000004128 high performance liquid chromatography Methods 0.000 description 4
- 229910052740 iodine Inorganic materials 0.000 description 4
- 239000010410 layer Substances 0.000 description 4
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 4
- LPNYRYFBWFDTMA-UHFFFAOYSA-N potassium tert-butoxide Chemical compound [K+].CC(C)(C)[O-] LPNYRYFBWFDTMA-UHFFFAOYSA-N 0.000 description 4
- 230000035755 proliferation Effects 0.000 description 4
- 125000006239 protecting group Chemical group 0.000 description 4
- 239000012312 sodium hydride Substances 0.000 description 4
- 229910000104 sodium hydride Inorganic materials 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- 239000000725 suspension Substances 0.000 description 4
- 238000005406 washing Methods 0.000 description 4
- OTLNPYWUJOZPPA-UHFFFAOYSA-N 4-nitrobenzoic acid Chemical compound OC(=O)C1=CC=C([N+]([O-])=O)C=C1 OTLNPYWUJOZPPA-UHFFFAOYSA-N 0.000 description 3
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 3
- 239000000654 additive Substances 0.000 description 3
- 230000000996 additive effect Effects 0.000 description 3
- 229940024606 amino acid Drugs 0.000 description 3
- 150000001413 amino acids Chemical class 0.000 description 3
- 239000002775 capsule Substances 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 229910052801 chlorine Inorganic materials 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 238000002425 crystallisation Methods 0.000 description 3
- 230000008025 crystallization Effects 0.000 description 3
- 239000002274 desiccant Substances 0.000 description 3
- 239000003814 drug Substances 0.000 description 3
- 238000004992 fast atom bombardment mass spectroscopy Methods 0.000 description 3
- 229910052731 fluorine Inorganic materials 0.000 description 3
- 125000001153 fluoro group Chemical group F* 0.000 description 3
- 239000008187 granular material Substances 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 238000001727 in vivo Methods 0.000 description 3
- 230000005764 inhibitory process Effects 0.000 description 3
- 238000002347 injection Methods 0.000 description 3
- 239000007924 injection Substances 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 150000007530 organic bases Chemical class 0.000 description 3
- 230000001590 oxidative effect Effects 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- APSBXTVYXVQYAB-UHFFFAOYSA-M sodium docusate Chemical compound [Na+].CCCCC(CC)COC(=O)CC(S([O-])(=O)=O)C(=O)OCC(CC)CCCC APSBXTVYXVQYAB-UHFFFAOYSA-M 0.000 description 3
- JXAZAUKOWVKTLO-UHFFFAOYSA-L sodium pyrosulfate Chemical compound [Na+].[Na+].[O-]S(=O)(=O)OS([O-])(=O)=O JXAZAUKOWVKTLO-UHFFFAOYSA-L 0.000 description 3
- 239000003826 tablet Substances 0.000 description 3
- 125000004213 tert-butoxy group Chemical group [H]C([H])([H])C(O*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 3
- ZYJPUMXJBDHSIF-NSHDSACASA-N (2s)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-3-phenylpropanoic acid Chemical compound CC(C)(C)OC(=O)N[C@H](C(O)=O)CC1=CC=CC=C1 ZYJPUMXJBDHSIF-NSHDSACASA-N 0.000 description 2
- 150000005207 1,3-dihydroxybenzenes Chemical class 0.000 description 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 2
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 2
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 2
- QOSSAOTZNIDXMA-UHFFFAOYSA-N Dicylcohexylcarbodiimide Chemical compound C1CCCCC1N=C=NC1CCCCC1 QOSSAOTZNIDXMA-UHFFFAOYSA-N 0.000 description 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 description 2
- 229930194542 Keto Natural products 0.000 description 2
- 125000003412 L-alanyl group Chemical group [H]N([H])[C@@](C([H])([H])[H])(C(=O)[*])[H] 0.000 description 2
- 125000000174 L-prolyl group Chemical group [H]N1C([H])([H])C([H])([H])C([H])([H])[C@@]1([H])C(*)=O 0.000 description 2
- 125000003580 L-valyl group Chemical group [H]N([H])[C@]([H])(C(=O)[*])C(C([H])([H])[H])(C([H])([H])[H])[H] 0.000 description 2
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
- 238000006751 Mitsunobu reaction Methods 0.000 description 2
- 102000010909 Monoamine Oxidase Human genes 0.000 description 2
- 108010062431 Monoamine oxidase Proteins 0.000 description 2
- JGFZNNIVVJXRND-UHFFFAOYSA-N N,N-diisopropylethylamine Substances CCN(C(C)C)C(C)C JGFZNNIVVJXRND-UHFFFAOYSA-N 0.000 description 2
- FZERHIULMFGESH-UHFFFAOYSA-N N-phenylacetamide Chemical compound CC(=O)NC1=CC=CC=C1 FZERHIULMFGESH-UHFFFAOYSA-N 0.000 description 2
- KFSLWBXXFJQRDL-UHFFFAOYSA-N Peracetic acid Chemical compound CC(=O)OO KFSLWBXXFJQRDL-UHFFFAOYSA-N 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical class [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 2
- ODFJOVXVLFUVNQ-UHFFFAOYSA-N acetarsol Chemical compound CC(=O)NC1=CC([As](O)(O)=O)=CC=C1O ODFJOVXVLFUVNQ-UHFFFAOYSA-N 0.000 description 2
- WETWJCDKMRHUPV-UHFFFAOYSA-N acetyl chloride Chemical compound CC(Cl)=O WETWJCDKMRHUPV-UHFFFAOYSA-N 0.000 description 2
- 239000012346 acetyl chloride Substances 0.000 description 2
- YWAAKSBJISUYNU-UHFFFAOYSA-N buta-1,2-dien-1-one Chemical class CC=C=C=O YWAAKSBJISUYNU-UHFFFAOYSA-N 0.000 description 2
- FJDQFPXHSGXQBY-UHFFFAOYSA-L caesium carbonate Chemical compound [Cs+].[Cs+].[O-]C([O-])=O FJDQFPXHSGXQBY-UHFFFAOYSA-L 0.000 description 2
- 229910000024 caesium carbonate Inorganic materials 0.000 description 2
- 230000003197 catalytic effect Effects 0.000 description 2
- 230000004663 cell proliferation Effects 0.000 description 2
- 210000003169 central nervous system Anatomy 0.000 description 2
- 125000001309 chloro group Chemical group Cl* 0.000 description 2
- 238000004440 column chromatography Methods 0.000 description 2
- QTMDXZNDVAMKGV-UHFFFAOYSA-L copper(ii) bromide Chemical compound [Cu+2].[Br-].[Br-] QTMDXZNDVAMKGV-UHFFFAOYSA-L 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 238000004821 distillation Methods 0.000 description 2
- 239000003480 eluent Substances 0.000 description 2
- 238000010265 fast atom bombardment Methods 0.000 description 2
- 238000007667 floating Methods 0.000 description 2
- 238000005194 fractionation Methods 0.000 description 2
- 229960002989 glutamic acid Drugs 0.000 description 2
- 229910052736 halogen Inorganic materials 0.000 description 2
- 230000002401 inhibitory effect Effects 0.000 description 2
- 239000011630 iodine Substances 0.000 description 2
- INQOMBQAUSQDDS-UHFFFAOYSA-N iodomethane Chemical compound IC INQOMBQAUSQDDS-UHFFFAOYSA-N 0.000 description 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 2
- 239000012280 lithium aluminium hydride Substances 0.000 description 2
- KWGKDLIKAYFUFQ-UHFFFAOYSA-M lithium chloride Chemical compound [Li+].[Cl-] KWGKDLIKAYFUFQ-UHFFFAOYSA-M 0.000 description 2
- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 2
- 125000001160 methoxycarbonyl group Chemical group [H]C([H])([H])OC(*)=O 0.000 description 2
- QPJVMBTYPHYUOC-UHFFFAOYSA-N methyl benzoate Chemical compound COC(=O)C1=CC=CC=C1 QPJVMBTYPHYUOC-UHFFFAOYSA-N 0.000 description 2
- 239000012046 mixed solvent Substances 0.000 description 2
- 210000004400 mucous membrane Anatomy 0.000 description 2
- OKDQKPLMQBXTNH-UHFFFAOYSA-N n,n-dimethyl-2h-pyridin-1-amine Chemical compound CN(C)N1CC=CC=C1 OKDQKPLMQBXTNH-UHFFFAOYSA-N 0.000 description 2
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 229910052763 palladium Inorganic materials 0.000 description 2
- 125000006340 pentafluoro ethyl group Chemical group FC(F)(F)C(F)(F)* 0.000 description 2
- 230000004962 physiological condition Effects 0.000 description 2
- 229910052697 platinum Inorganic materials 0.000 description 2
- CHKVPAROMQMJNQ-UHFFFAOYSA-M potassium bisulfate Chemical compound [K+].OS([O-])(=O)=O CHKVPAROMQMJNQ-UHFFFAOYSA-M 0.000 description 2
- 229910000343 potassium bisulfate Inorganic materials 0.000 description 2
- RIBFXMJCUYXJDZ-UHFFFAOYSA-N propanoyl bromide Chemical compound CCC(Br)=O RIBFXMJCUYXJDZ-UHFFFAOYSA-N 0.000 description 2
- BBFCIBZLAVOLCF-UHFFFAOYSA-N pyridin-1-ium;bromide Chemical compound Br.C1=CC=NC=C1 BBFCIBZLAVOLCF-UHFFFAOYSA-N 0.000 description 2
- 239000012266 salt solution Substances 0.000 description 2
- FSYKKLYZXJSNPZ-UHFFFAOYSA-N sarcosine Chemical compound C[NH2+]CC([O-])=O FSYKKLYZXJSNPZ-UHFFFAOYSA-N 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- 239000000741 silica gel Substances 0.000 description 2
- 229910002027 silica gel Inorganic materials 0.000 description 2
- 229960001866 silicon dioxide Drugs 0.000 description 2
- 235000017557 sodium bicarbonate Nutrition 0.000 description 2
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 2
- 239000012279 sodium borohydride Substances 0.000 description 2
- 229910000033 sodium borohydride Inorganic materials 0.000 description 2
- QDRKDTQENPPHOJ-UHFFFAOYSA-N sodium ethoxide Chemical compound [Na+].CC[O-] QDRKDTQENPPHOJ-UHFFFAOYSA-N 0.000 description 2
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical class O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 2
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- 125000001360 methionine group Chemical group N[C@@H](CCSC)C(=O)* 0.000 description 1
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- PSHKMPUSSFXUIA-UHFFFAOYSA-N n,n-dimethylpyridin-2-amine Chemical compound CN(C)C1=CC=CC=N1 PSHKMPUSSFXUIA-UHFFFAOYSA-N 0.000 description 1
- 125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 description 1
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- LIGACIXOYTUXAW-UHFFFAOYSA-N phenacyl bromide Chemical compound BrCC(=O)C1=CC=CC=C1 LIGACIXOYTUXAW-UHFFFAOYSA-N 0.000 description 1
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- 125000001501 propionyl group Chemical group O=C([*])C([H])([H])C([H])([H])[H] 0.000 description 1
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- PBMFSQRYOILNGV-UHFFFAOYSA-N pyridazine Chemical group C1=CC=NN=C1 PBMFSQRYOILNGV-UHFFFAOYSA-N 0.000 description 1
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- 239000006188 syrup Substances 0.000 description 1
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- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 238000011287 therapeutic dose Methods 0.000 description 1
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- 238000002560 therapeutic procedure Methods 0.000 description 1
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- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 125000003866 trichloromethyl group Chemical group ClC(Cl)(Cl)* 0.000 description 1
- ITMCEJHCFYSIIV-UHFFFAOYSA-N triflic acid Chemical compound OS(=O)(=O)C(F)(F)F ITMCEJHCFYSIIV-UHFFFAOYSA-N 0.000 description 1
- 125000003774 valeryl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
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Landscapes
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
A 3-phenyl-cinnoline homologue or a physiologically acceptable salt thereof; and a cytostatic agent or antitumor agent comprising the same as an active constituent.
Description
Technical field
The present invention relates to acceptable salt on 3-phenyl-cinnolines analogue or its physiology and comprise this analogue or its physiology on acceptable salt as the antineoplastic agent of active ingredient.
Background technology
Malignant tumour is the cell group that continues to run counter to the proliferation in vivo of normal biology mechanism, unless obtain suitable treatment, otherwise cause host's death.Usually adopt surgical discectomy, radiation exposure, hormonotherapy or chemotherapy to treat malignant tumour, especially surgical operation is the first-selection of treatment malignant solid tumor.Radiotherapy, hormonotherapy and chemotherapy are used before operation or as postoperative replacement therapy usually, or are used for being predicated the treatment that can not pass through the malignant solid tumor of operative treatment.Hormonotherapy and chemotherapy are used to make the zone of surgical discectomy to dwindle, or be used to make can not be fully by tumour regression and the disappearance and the prophylaxis of tumours recurrence of surgical resection.Yet these operations at present cause the misery of the patient physiological of suffering from cancer and psychology, and further when metastases, must enlarge the surgical blanking zone, and surgical technic that need be more difficult.Chemotherapy is not that the reason of main therapy is that the antineoplastic agent that does not cause serious side effects and demonstrate clinical effectiveness is not also developed.Therefore, need a kind of antineoplastic agent that has outstanding antitumous effect at malignant solid tumor.
In the non-patent literature 1 hereinafter, reported that cinnoline derivatives acts on central nervous system, in non-patent literature 2, reported to have the inhibiting cinnoline derivatives of monoamine oxidase.Yet these two pieces of documents had not both illustrated the cinnolines analogue of the present invention by following general formula (1) representative, and the anti-tumor activity of cinnolines analogue is not described yet.
In the non-patent literature 3 below, described the synthetic and reaction of cinnoline derivatives, yet the antitumor action of cinnolines analogue has not been described.
Reference:
[non-patent literature 1]
People such as Rashmi K.Shah, Central Nervous System Active5-oxo-1,4,5,6,7,8-Hexahydrocinnolines, Journal of MedicinalChemistry, 1976, vol.19, p.508-511
(non-patent literature 2)
People such as Angelo Carotti, Inhibition of Monoamine Oxidase-B byCondensed Pyridazines and Pyrimidines:Effects ofLipophilicity and Structure-Activity Relationships, Jounal ofMedicinal Chemistry, 1998, vol.41, p.3812-3820
(non-patent literature 3)
People such as K.Nagarajan, Synthesis ﹠amp; Reactions of4,6,7,8-Tetrahydro-5 (1H)-cinnolinones, Indian Journal ofChemistry, 1986, vol.25B, p.697-708
Summary of the invention
The present inventor finds that 3-phenyl-cinnolines analogue or its pharmacy acceptable salt have the restraining effect and the anti-tumor activity of cell proliferation, and has therefore finished the present invention.
The present invention relates to following 1)-14) aspect.
1. comprise by acceptable salt on the 3-phenyl-cinnolines analogue of following general formula (1) or (2) representative or its physiology as the antineoplastic agent of active ingredient:
Wherein J is A-C-B (C is a carbon atom); A is that (O is a Sauerstoffatom to the O-Y group; Y is a hydrogen atom, the low alkyl group that can be replaced by phenyl, lower acyl or can protected amino-acid residue);
B is a hydrogen atom, low alkyl group, or form the imino-of carbonyl or replacement with A;
K is (CH
2)
q
L is N-W (N is a nitrogen-atoms) or W-C-W ' (C is a carbon atom);
Each is to have the low alkyl group that is selected from hydroxyl, lower alkoxy and phenyl substituent independently for W and W ', phenyl, carboxyl, lower alkoxycarbonyl or hydrogen atom;
M is (CH
2)
m, or J-K-L-M is C (O-Y)=CH-C (W)-CH (Y has identical implication with W hereinbefore);
Z is Sauerstoffatom or N-Q (Q is amino, low-grade alkyl amino, hydroxyl or lower alkoxy);
Each is low alkyl group independently for X and X ', lower alkoxycarbonyl, rudimentary amido, lower alkoxy, junior alkyl halides, nitro, cyano group, halogen atom or hydrogen atom; Each is 0 to 3 integer independently for m and q;
And each is 0 or 1 independently for n and n '.
2. according to the antineoplastic agent described in top 1, wherein 3-phenyl-cinnolines analogue is by the represented compound of following general formula (3):
Wherein A be the O-Y group (Y is a hydrogen atom, the low alkyl group that can be replaced by phenyl, lower acyl or can protected amino-acid residue);
B is a hydrogen atom, low alkyl group, or form the imino-of carbonyl or replacement with A;
L is N-W or W-C-W ';
Each is to have the low alkyl group that is selected from hydroxyl, lower alkoxy and phenyl substituent independently for W and W ', phenyl, carboxyl, lower alkoxycarbonyl or hydrogen atom;
X is a low alkyl group, lower alkoxycarbonyl, rudimentary amido, lower alkoxy, trifluoromethyl, nitro, cyano group or halogen atom;
X ' is a low alkyl group, lower alkoxycarbonyl, rudimentary amido, lower alkoxy, trifluoromethyl, nitro, cyano group, halogen atom or hydrogen atom; Each is 0 to 3 integer independently for m and q;
And each is 0 or 1 independently for n and n '.
3. according to the antineoplastic agent described in top 2, wherein B is a hydrogen atom;
L is W-C-W ';
Each is to have the low alkyl group that is selected from hydroxyl, lower alkoxy and phenyl substituent independently for W and W ', or hydrogen atom;
X is the 3-trifluoromethyl, 3-nitro, 3-cyano group or 3-bromine group;
X ' is a hydrogen atom;
Each is respectively 1 for m and q;
N is 0 or 1; And n ' is 0.
4. according to the antineoplastic agent described in above-mentioned 3, wherein W and W ' each be hydrogen atom or low alkyl group independently, and X is the 3-trifluoromethyl.
5. according to the antineoplastic agent described in above-mentioned 2, wherein Y is the glycyl group, alanyl group, valyl group or α-Gu Anxianji group; B is a hydrogen atom; L is H-C-CH
3X is the 3-trifluoromethyl; X ' is a hydrogen atom; Each is respectively 1 for m and q; And n is 0 or 1; N ' is 0.
6. according to the antineoplastic agent described in above-mentioned 1, wherein 3-phenyl-cinnolines analogue is by the represented compound of following general formula (4):
Wherein X and X ' each be low alkyl group independently, lower alkoxycarbonyl, rudimentary amido, lower alkoxy, trifluoromethyl, nitro, cyano group, halogen atom or hydrogen atom; Y is can be by the low alkyl group of phenyl, lower acyl or hydrogen atom replacement; W can have the low alkyl group that is selected from hydroxyl, lower alkoxy and phenyl substituent, phenyl, carboxyl, lower alkoxycarbonyl or a hydrogen atom.
7. according to the antineoplastic agent described in above-mentioned 6, wherein X is a trifluoromethyl, nitro, cyano group or halogen atom; X ' is a hydrogen atom; W can have the low alkyl group that is selected from hydroxyl, lower alkoxy and phenyl substituent.
8. according to the antineoplastic agent described in above-mentioned 7, wherein X is the 3-trifluoromethyl, 3-nitro, 3-cyano group or 3-halogen atom; W is the low alkyl group of non-replacement.
9. according to the antineoplastic agent described in above-mentioned 1, wherein 3-phenyl-cinnolines analogue is by the represented compound of following general formula (5):
Wherein W and W ' each be hydrogen atom or low alkyl group independently; X is a junior alkyl halides; Z is Sauerstoffatom or N-Q; Q is amino, low-grade alkyl amino, hydroxyl or lower alkoxy.
10. according to the antineoplastic agent described in above-mentioned 9, wherein W is hydrogen atom or methyl; W ' is hydrogen atom or methyl; X is the 3-trifluoromethyl; Z is a Sauerstoffatom.
11. according to the antineoplastic agent described in above-mentioned 9, wherein W is hydrogen atom or methyl; W ' is hydrogen atom or methyl; X is the 3-trifluoromethyl; Z is N-NH
2
12. according to the antineoplastic agent described in above-mentioned 1, wherein 3-phenyl cinnolines analogue is 7-methyl-3-(3-trifluoromethyl)-7,8-dihydro-6H-cinnolines-5-ketone; 7-methyl-3-(3-trifluoromethyl)-5,6,7; 8-tetrahydrochysene cinnolines-5-alcohol, 7-methyl-3-(3-trifluoromethyl) cinnolines-5-alcohol, 7-methyl isophthalic acid-oxo-3-(3-trifluoromethyl)-5; 6,7,8-tetrahydrochysene cinnolines-5-alcohol; 5-glycyl oxygen base-7-methyl-3-(3-trifluoromethyl)-5; 6,7,8-tetrahydrochysene cinnolines; 5-(L-alanyl) oxygen base-7-methyl-3-(3-trifluoromethyl)-5; 6,7,8-tetrahydrochysene cinnolines; 5-(L-valyl) oxygen base-7-methyl-3-(3-trifluoromethyl)-5; 6,7,8-tetrahydrochysene cinnolines; 5-(L-α-Gu Anxianji) oxygen base-7-methyl-3-(3-trifluoromethyl)-5; 6,7,8-tetrahydrochysene cinnolines.
13. comprise according to described in the above-mentioned 1-12 each 3-phenyl-cinnolines analogue or its physiology on acceptable salt as the inhibition of cell proliferation of active ingredient.
14. according to described in the above-mentioned 1-12 each 3-phenyl-cinnolines analogue or its physiology on acceptable salt, condition is not comprise that wherein Z is the compound of Sauerstoffatom.
Preferred forms of the present invention
Antineoplastic agent of the present invention contains by acceptable salt on the represented 3-phenyl-cinnolines analogue in above-mentioned general formula (1) or (2) or its physiology as active ingredient.
If do not give a definition in addition, in the substituting group in general formula (1) or (2), " low alkyl group " is meant, has the straight or branched alkyl of 1 to 6 carbon atom, for example, methyl, ethyl, n-propyl, sec.-propyl, normal-butyl, sec-butyl, the tertiary butyl, n-pentyl, isopentyl, neo-pentyl, n-hexyl, or the like, preferred group comprises methyl, ethyl and sec.-propyl, and particularly preferred group is a methyl.
If do not give a definition in addition, in the substituting group in general formula (1) or (2), " lower acyl " is meant; straight or branched carboxyl groups with non-replacement of 1 to 6 carbon atom, for example, formyl radical; ethanoyl, propionyl, positive butyryl radicals; isobutyryl, valeryl group, isovaleryl group; the pivalyl group; the hexanoyl group, or the like, preferred group is an ethanoyl.
Advance-go on foot, in the substituting group of general formula (1), " amino-acid residue of optional protection " comprises the a-amino acid residue that is commonly called indispensable amino acid, and side chain wherein and/or N-terminal can be protected, and condition is that absolute configuration can be L or D.The ester bond that preferably on main chain or side chain, forms with the key of Sauerstoffatom with carboxyl.The example of protection functional group comprises amino, carboxyl, and guanidine radicals, hydroxyl, thiol group, or the like.Be not particularly limited protecting group, and the protecting group of using can be included in common peptide building-up reactions.The example of representational protecting group comprises particularly: carbalkoxy is tertbutyloxycarbonyl and carbobenzoxy-(Cbz) for example; Alkyl is methyl for example, the tertiary butyl and benzyl; With acyl group for example ethanoyl and benzoyl.Can comprise by protected amino-acid residue: N-(tertbutyloxycarbonyl)-L-valyl group; O-benzyl-D-tyrosyl group; N-(tertbutyloxycarbonyl)-L-prolyl group; N-(tertbutyloxycarbonyl)-L-phenylalanyl group; L-alanyl group, L-valyl group, L-α-Gu Anxianji group; the glycyl group, or the like.Preferred group comprises L-alanyl group, L-valyl group, L-α-Gu Anxianji group, glycyl group or the like.
In the substituting group of general formula (1), the example of the low alkyl group that is replaced by phenyl comprises particularly: benzyl, and the 1-styroyl, the 2-styroyl, benzyl or the like, and preferred benzyl, or the like.
In the substituting group of general formula (1) or (2), " lower alkoxy " is meant, has the straight or branched alkoxyl group of 1 to 6 carbon atom, for example, methoxyl group, oxyethyl group, positive propoxy, isopropoxy, n-butoxy, isobutoxy, tert.-butoxy, n-pentyloxy, isopentyloxy, positive hexyloxy, or the like, and wherein methoxyl group and oxyethyl group are preferred group.
In the substituting group of general formula (1) or (2), have " low alkyl group " that be selected from hydroxyl, lower alkoxy and phenyl substituent, be meant to have one or more identical or different substituent low alkyl groups, comprise methylol particularly, 2-hydroxyl-2-propyl group, benzyl, methoxymethyl, or the like, preferred methylol and benzyl, or the like.
In general formula (1) or (2), " L is N (nitrogen-atoms)-W " is meant the aliphatics heterocycle that contains the nitrogen-atoms that is replaced by W.The concrete example of L comprises the N-methyl, the N-benzyl, and the N-methoxymethyl, N-(2-hydroxyl) methyl, or the like, preferred N-benzyl and N-methyl.
In general formula (1) or (2), " L is W-C (carbon atom)-W ' " is meant by the aliphatics carbocyclic ring of W and W ' replacement.The object lesson of W and W ' is, W is that hydrogen atom and W ' they are methyl, ethyl, sec.-propyl, ethoxycarbonyl, carboxyl, methylol, 2-hydroxyl-2-propyl group, phenyl or hydrogen atom, or the like, or W and two of W ' be methyl, or the like.Preferably, W is that hydrogen atom and W ' are methyl or sec.-propyl.
In general formula (1) or (2), " lower alkoxycarbonyl " is meant the group of above-mentioned lower alkoxy and carbonyl bonding, specifically comprises methoxycarbonyl, ethoxycarbonyl, the third oxygen carbonyl, preferred methoxycarbonyl and ethoxycarbonyl.
In general formula (1) or (2), " low-grade alkyl amino " is meant in the above-mentioned low alkyl group one or two group with nitrogen atom bonding, specifically comprises methylamino, dimethylamino, ethylamino, diethylamino, amino and two (n-propyl) amino of n-propyl, or the like.
In general formula (1), J represents " A-C (carbon atom)-B ", and wherein A and B can form the imino-(C=N-(substituting group)) of carbonyl (C=0) or replacement.Substituent example in the imino-that replaces is amino, low-grade alkyl amino, hydroxyl or lower alkoxy or the like.
In general formula (1) or (2), the example of " halogen atom " is a fluorine atom, chlorine atom, bromine atoms or iodine atom, preferred bromine atoms or fluorine atom.
In general formula (1) or (2), " rudimentary amido " comprises the amino with above-mentioned lower acyl bonding, particularly, for example, formamido group, kharophen, propionamido or the like, preferred kharophen.
In general formula (1) or (2), the low alkyl group in " junior alkyl halides " is the group identical with above-mentioned low alkyl group, and preferred group is also identical with above-mentioned preferred group.Halogen atom in " junior alkyl halides " comprises atom similar to the above, i.e. fluorine atom, chlorine atom, bromine atoms or iodine atom.The replacement number that comprises halogen atom in the present invention is the desirable algebraically order to maximum, and under the situation of multiple replacement, the halogen atom of replacement can be identical or different.1-chloropropyl particularly, trichloromethyl, trifluoromethyl, 1,1, the 1-trifluoroethyl, pentafluoroethyl group and 1,1-two fluoro-1-chloroethyls, preferred pentafluoroethyl group, trifluoromethyl, or the like, preferred especially trifluoromethyl.
" J-K-L-M is C (O-Y)=CH-C (W)=CH (Y and W have implication same as described above) " is meant cinnolines skeleton structure, phenyl ring wherein and pyridazine cyclic condensation.Particularly, for example, it is the compound by above-mentioned general formula (4) expression.
In general formula (1) or (2), X and X ' are positioned on the phenyl ring as substituting group, do not limit its position particularly.Therefore, its all isomer is included in the scope of the present invention, and preferred in the position single substituting group of 3.Preferred substituted comprises trifluoromethyl, nitro, cyano group, bromine atoms, preferred especially 3-trifluoromethyl.
In general formula of the present invention (1), each m and q are 0 to 3 integer independently, and 4-10 is provided unit ring, form the fused rings with the pyridazine ring, preferred 5-7 unit ring, and more preferably 6 yuan of rings, wherein m and q represent 1.
In general formula of the present invention (1), " n, n ' are 1 " is meant the N-oxide compound, and preferred n and n ' are 0, or each of n and n ' is 1.
As the active ingredient 3-phenyl-cinnolines analogue of antineoplastic agent of the present invention, in being also included within by the compound of above general formula (3) expression.In the compound of general formula (3); the low alkyl group that can be replaced by phenyl, lower acyl can protected amino-acid residue; low alkyl group; lower alkoxy, phenyl, lower alkoxycarbonyl; rudimentary amido; the imino-of halogen atom and replacement, have with general formula (1) in the identical meaning of each substituting group, and preferred group also is with above mentioned identical.Further, m, each m among the q, n and n ' and general formula (1), q, n is identical with n ', and preferable range also is identical.
In the compound of most preferred general formula (3), B is a hydrogen atom; L is W-C-W '; Each is to choose wantonly to have the low alkyl group that is selected from hydroxyl, lower alkoxy and phenyl substituent independently for W and W ', or hydrogen atom; X is the 3-trifluoromethyl, 3-nitro, 3-cyano group or 3-bromine group; X ' is a hydrogen atom; Two of m and q 1; N is 0 or 1; And n ' is 0.In a preferred compound, each is hydrogen atom or low alkyl group independently for W and W '; X is the 3-trifluoromethyl.In in addition preferred compound, Y is the glycyl group, alanyl group, valyl group or α-Gu Anxianji group; B is a hydrogen atom; L is H-C-CH
3X is the 3-trifluoromethyl; X ' is a hydrogen atom; Two of m and q are 1; N is 0 or 1; N ' is 0.
The example of the compound of general formula (3) comprises as the compound as shown in specifically in table 1.In table, Ph represents phenyl, and Et represents ethyl, and Me represents methyl, and Ac represents ethanoyl, and Bn represents benzyl, and Boc represents tertbutyloxycarbonyl, and t-Bu represents the tertiary butyl; Mix is meant cis and trans mixture; Amino acid uses abbreviation to express usually.
Table 1
Compound number | A,B | L | The isomer type | q | m | n | n′ | X | X′ | Opticity |
1 | =O | C(H)Ph | - | 1 | 1 | 0 | 0 | 3-CF3 | H | (±) |
2 | =O | COOEt | - | 1 | 1 | 0 | 0 | 3-CF3 | H | (±) |
3 | -OH,H | COOEt | syn | 1 | 1 | 0 | 0 | 3-CF3 | H | (±) |
4 | -OH,H | COOH | syn | 1 | 1 | 0 | 0 | 3-CF3 | H | (±) |
5 | =O | COOH | - | 1 | 1 | 0 | 0 | 3-CF3 | H | (±) |
6 | -OH,H | C(H)Me | syn | 1 | 1 | 0 | 0 | 3-CF3 | H | (±) |
7 | -OH,H | C(H)Me | anti | 1 | 1 | 0 | 0 | 3-CF3 | H | (±) |
8 | -O-Pro(Boc),H | C(H)Me | anti | 1 | 1 | 0 | 0 | 3-CF3 | H | (±) |
syn | 1 | 1 | 0 | 0 | 3-CF3 | H | (±),(-) | |||
9 | -OH,H | C(H)Me | syn | 1 | 1 | 0 | 0 | 3-CF3 | H | (5R,7R) |
10 | -OH,H | C(H)Me | syn | 1 | 1 | 0 | 0 | 3-CF3 | H | (5S,7S) |
11 | -OAc,H | C(H)Me | syn | 1 | 1 | 0 | 0 | 3-CF3 | H | (±) |
12 | -OH,H | C(H)Me | syn | 1 | 1 | 1 | 0 | 3-CF3 | H | (±) |
13 | =O | C(H)Me | - | 1 | 1 | 1 | 0 | 3-CF3 | H | (±) |
14 | -OH,H | C(H)CH2OH | mix | 1 | 1 | 0 | 0 | 3-CF3 | H | (±) |
15 | =O | C(H)Me | - | 1 | 1 | 0 | 0 | 3-CN | H | (±) |
16 | -OH,H | C(H)Me | syn | 1 | 1 | 0 | 0 | 3-CN | H | (±) |
17 | -OH,H | C(Me)2 | - | 1 | 1 | 0 | 0 | 3-CF3 | H | (±) |
18 | -OH,H | CH2 | - | 1 | 1 | 0 | 0 | 3-CF3 | H | (±) |
19 | =O | C(H)Me | - | 1 | 1 | 0 | 0 | 3-Br | H | (±) |
20 | =O | C(H)Me | - | 1 | 1 | 0 | 0 | 3-NO2 | H | (±) |
21 | =O | C(H)Me | - | 1 | 1 | 0 | 0 | 3-Me | H | (±) |
22 | =O | C(H)Me | - | 1 | 1 | 0 | 0 | 3-CO2Me | H | (±) |
23 | =O | C(H)Me | - | 1 | 1 | 0 | 0 | 3-NHAc | H | (±) |
24 | =O | C(H)Me | - | 1 | 1 | 0 | 0 | 3-F | H | (±) |
25 | =O | C(H)Me | - | 1 | 1 | 0 | 0 | 3-OMe | H | (±) |
26 | =O | NBn | - | 1 | 1 | 0 | 0 | 3-CF3 | H | - |
27 | -OH,Me | CH-C(Me)2OH | mix | 1 | 1 | 0 | 0 | 3-CF3 | H | (±) |
28 | =O | C(H)Me | - | 1 | 1 | 0 | 0 | 3-F | 5-CF3 | (±) |
29 | -OH,H | C(H)Me | syn | 1 | 1 | 0 | 0 | 3-F | 5-CF3 | (±) |
30 | -OH,Me | C(H)Me | mix | 1 | 1 | 0 | 0 | 3-CF3 | H | (±) |
31 | -O-Ala(Boc),H | C(H)Me | syn | 1 | 1 | 0 | 0 | 3-CF3 | H | Individual isomer |
32 | -O-Ala,H | C(H)Me | syn | 1 | 1 | 0 | 0 | 3-CF3 | H | Individual isomer |
33 | -O-Asp(α)(Boc) (β)(OtBu),H | C(H)Me | syn | 1 | 1 | 0 | 0 | 3-CF3 | H | Individual isomer |
34 | -O-Asp(α),H | C(H)Me | syn | 1 | 1 | 0 | 0 | 3-CF3 | H | Individual isomer |
35 | -O-Asp(β)(Boc)(α) (OtBu),H | C(H)Me | syn | 1 | 1 | 0 | 0 | 3-CF3 | H | Individual isomer |
36 | -O-Asp(β),H | C(H)Me | syn | 1 | 1 | 0 | 0 | 3-CF3 | H | Individual isomer |
37 | -O-Glu(α)(Boc)(Y) (OtBu),H | C(H)Me | syn | 1 | 1 | 0 | 0 | 3-CF3 | H | Individual isomer |
38 | -O-Glu(α),H | C(H)Me | syn | 1 | 1 | 0 | 0 | 3-CF3 | H | Individual isomer |
39 | -O- Glu(Y)(Boc)(α)(Ot Bu),H | C(H)Me | syn | 1 | 1 | 0 | 0 | 3-CF3 | H | Individual isomer |
40 | -O-Glu(Y),H | C(H)Me | syn | 1 | 1 | 0 | 0 | 3-CF3 | H | Individual isomer |
41 | -O-Gly(Boc),H | C(H)Me | syn | 1 | 1 | 0 | 0 | 3-CF3 | H | Individual isomer |
42 | -O-Gly,H | C(H)Me | syn | 1 | 1 | 0 | 0 | 3-CF3 | H | Individual isomer |
43 | -O-Leu(Boc),H | C(H)Me | syn | 1 | 1 | 0 | 0 | 3-CF3 | H | Individual isomer |
44 | -O-Leu,H | C(H)Me | syn | 1 | 1 | 0 | 0 | 3-CF3 | H | Individual isomer |
45 | -O-Lys(Boc),H | C(H)Me | syn | 1 | 1 | 0 | 0 | 3-CF3 | H | Individual isomer |
46 | -O-Lys,H | C(H)Me | syn | 1 | 1 | 0 | 0 | 3-CF3 | H | Individual isomer |
47 | -O-Met(Boc),H | C(H)Me | syn | 1 | 1 | 0 | 0 | 3-CF3 | H | Individual isomer |
48 | -O-Met,H | C(H)Me | syn | 1 | 1 | 0 | 0 | 3-CF3 | H | Individual isomer |
49 | -O-Phe(Boc),H | C(H)Me | syn | 1 | 1 | 0 | 0 | 3-CF3 | H | Individual isomer |
50 | -O-Phe,H | C(H)Me | syn | 1 | 1 | 0 | 0 | 3-CF3 | H | Individual isomer |
51 | -O-Pro,H | C(H)Me | syn | 1 | 1 | 0 | 0 | 3-CF3 | H | Individual isomer |
52 | -O-Val(Boc),H | C(H)Me | syn | 1 | 1 | 0 | 0 | 3-CF3 | H | (5S,7S) |
53 | -O-Val,H | C(H)Me | syn | 1 | 1 | 0 | 0 | 3-CF3 | H | (5S,7S) |
54 | -OH,H | CH2 | - | 1 | 0 | 0 | 0 | 3-CF3 | H | (±) |
55 | -OH,H | CH2 | - | 0 | 1 | 0 | 0 | 3-CF3 | H | (±) |
56 | -OH,H | CH2 | - | 1 | 2 | 0 | 0 | 3-CF3 | H | (±) |
57 | -OH,H | CH2 | - | 2 | 1 | 0 | 0 | 3-CF3 | H | (±) |
58 | -OH,H | CH2 | - | 2 | 2 | 0 | 0 | 3-CF3 | H | (±) |
59 | -OH,H | CH2 | - | 0 | 3 | 0 | 0 | 3-CF3 | H | (±) |
60 | -OH,H | C(H)Me | mix | 1 | 1 | 0 | 1 | 3-CF3 | H | (±) |
61 | -OH,H | CH2 | - | 1 | 1 | 0 | 0 | 3-CF3 | H | (±) |
62 | -OH,H | C(H)Me | syn | 1 | 1 | 0 | 0 | 3-CF3 | 5-CF3 | (±) |
63 | -OBn,H | C(H)Me | syn | 1 | 1 | 0 | 0 | 3-CF3 | H | (±) |
64 | =O | NPh | - | 1 | 1 | 0 | 0 | 3-CF3 | H | - |
65 | =O | NCO2Me | - | 1 | 1 | 0 | 0 | 3-CF3 | H | - |
66 | -OH,H | C(H)CH2OMe | mix | 1 | 1 | 0 | 0 | 3-CF3 | H | (±) |
67 | -O-(D)-Phe(Boc),H | C(H)Me | syn | 1 | 1 | 0 | 0 | 3-CF3 | H | (5S,7S) |
68 | -O-Val(Boc),H | C(H)Me | syn | 1 | 1 | 0 | 0 | 3-CF3 | H | (5R,7R) |
69 | -O-Val,H | C(H)Me | syn | 1 | 1 | 0 | 0 | 3-CF3 | H | (5R,7R) |
70 | -O-Val(Boc),H | C(H)Me | anti | 1 | 1 | 0 | 0 | 3-CF3 | H | (5S,7R) |
71 | -OH,H | C(H)Me | anti | 1 | 1 | 0 | 0 | 3-CF3 | H | (5S,7R) |
72 | -O-Val,H | C(H)Me | anti | 1 | 1 | 0 | 0 | 3-CF3 | H | (5S,7R) |
73 | -O-Val(Boc),H | C(H)Me | anti | 1 | 1 | 0 | 0 | 3-CF3 | H | (5R,7S) |
74 | -OH,H | C(H)Me | anti | 1 | 1 | 0 | 0 | 3-CF3 | H | (5R,7S) |
75 | -O-Val,H | C(H)Me | anti | 1 | 1 | 0 | 0 | 3-CF3 | H | (5R,7S) |
76 | =O | C(Me)2 | - | 1 | 1 | 0 | 0 | 3-CF3 | H | - |
77 | =O | CH2 | - | 1 | 1 | 0 | 0 | 3-CF3 | H | - |
78 | =O | C(H)Me | - | 1 | 1 | 0 | 0 | 3-CH2Cl | H | (±) |
79 | =O | C(H)Me | - | 1 | 1 | 0 | 0 | 3-CF3 | H | (±) |
80 | =O | C(H)Et | - | 1 | 1 | 0 | 0 | 2-CH2Br | H | (±) |
81 | =O | C(H)Me | - | 1 | 1 | 0 | 0 | 4-C2F5 | H | (±) |
82 | =O | C(Me)2 | - | 1 | 1 | 0 | 0 | 3-CF3 | H | - |
83 | =N-NH2 | C(H)Me | - | 1 | 1 | 0 | 0 | 3-CF3 | H | (±) |
84 | =N-NHEt | C(H)iPr | - | 1 | 1 | 0 | 0 | 4-CH2Cl | H | (±) |
85 | =N-OMe | C(H)iPr | - | 1 | 1 | 0 | 0 | 2-CH2Cl | H | (±) |
86 | =N-OEt | C(Me)Et | - | 1 | 1 | 0 | 0 | 4-CF3 | H | (±) |
87 | -OH,H | C(H)Me | mix | 2 | 0 | 0 | 0 | 3-CF3 | H | (±) |
88 | =O | NMe | - | 1 | 1 | 0 | 0 | 3-CF3 | H | (±) |
89 | =O | NH | - | 1 | 1 | 0 | 0 | 3-CF3 | H | (±) |
90 | -OH,H | C(H)Me | mix | 1 | 1 | 1 | 1 | 3-CF3 | H | (±) |
As the active ingredient 3-phenyl-cinnolines analogue of antineoplastic agent of the present invention, comprise compound equally by above-mentioned general formula (4) expression.In the compound of general formula (4), low alkyl group, lower alkoxycarbonyl; rudimentary amido; lower alkoxy, trifluoromethyl, nitro; cyano group; halogen atom, the low alkyl group that can be replaced by phenyl, lower acyl; phenyl and carboxyl have with general formula (1) in the identical meaning of each substituting group, and preferred group equally with above mention identical.
In the compound of particularly preferred general formula (4), X is a trifluoromethyl, nitro, cyano group or halogen atom; X ' is a hydrogen atom; W can have the low alkyl group that is selected from hydroxyl, lower alkoxy and phenyl substituent.In preferred compound, K is the 3-trifluoromethyl, the 3-nitro, and 3-cyano group or 3-halogen atom, W are the low alkyl groups of non-replacement.
The example of the compound of general formula (4) specifically comprises,
3-(3-trifluoromethyl) cinnolines-5-alcohol,
7-methyl-3-(3-trifluoromethyl) cinnolines-5-alcohol,
7-phenyl-3-(3-trifluoromethyl) cinnolines-5-alcohol,
7-(2-methoxy ethyl)-3-(3-trifluoromethyl) cinnolines-5-alcohol,
7-ethoxycarbonyl-3-(3-trifluoromethyl) cinnolines-5-alcohol,
3-(3-cyano-phenyl)-7-methyl cinnolines-5-alcohol,
3-(2-ethylphenyl)-7-methyl cinnolines-5-alcohol,
3-(3-phenelyl)-7-methyl cinnolines-5-alcohol,
3-(3-acetylamino phenyl)-5-acetoxyl group-7-methyl cinnolines,
5-methoxyl group-7-methyl-3-(3-trifluoromethyl) cinnolines,
5-acetoxyl group-7-methyl-3-(3-trifluoromethyl) cinnolines,
5-benzyloxy-7-methyl-3-(3-trifluoromethyl) cinnolines,
5-acetoxyl group-7-methyl-3-(3-nitrophenyl) cinnolines,
3-(2-fluorophenyl)-7-sec.-propyl-5-methoxyl group cinnolines,
3-(3, the 5-bis trifluoromethyl phenyl)-7-hydroxymethyl cinnolines-5-alcohol,
7-benzyl-5-oxyethyl group-3-(2-methoxycarbonyl phenyl)-cinnolines,
3-(3-acetylamino phenyl) cinnolines-5-alcohol,
3-(2-chloro-5-trifluoromethyl)-5-hydroxyl cinnolines-7-carboxylic acid,
And 3-(2-fluoro-5-trifluoromethyl)-5-hydroxyl cinnolines-7-carboxylic acid, or the like.
Preferred 7-methyl-3-(3-trifluoromethyl) cinnolines-5-alcohol, 5-methoxyl group-7-methyl-3-(3-trifluoromethyl) cinnolines, 5-acetoxyl group-7-methyl-3-(3-trifluoromethyl)-cinnolines and 5-benzyloxy 7-methyl-3-(3-trifluoromethyl) cinnolines.
As the active ingredient 3-phenyl-cinnolines analogue of antineoplastic agent of the present invention, comprise compound by above-mentioned general formula (5) expression.In the compound of general formula (5), low alkyl group, junior alkyl halides, low-grade alkyl amino and lower alkoxy have with general formula (1) or (2) in the identical meaning of each substituting group, and preferred group is also with above mentioned identical.
In preferred compound, W is hydrogen atom or methyl; W ' is hydrogen atom or methyl; X is the 3-trifluoromethyl; Z is Sauerstoffatom or N-NH
2
The example of the compound of general formula (5) specifically comprises: 7-methyl-3-(3-trifluoromethyl)-4,6,7,8-tetrahydrochysene-1H-cinnolines-5-ketone, 7,7-dimethyl-3-(3-trifluoromethyl)-4,6,7,8-tetrahydrochysene-1H-cinnolines-5-ketone, 7-methyl-3-(4-chloromethyl phenyl)-4,6,7,8-tetrahydrochysene-1H-cinnolines-5-ketone, and 3-(3-trifluoromethyl)-4,6,7,8-tetrahydrochysene-1H-cinnolines-5-ketone, or the like.
Preferred example by the 3-phenyl-cinnolines analogue of above-mentioned general formula (1) expression specifically comprises: 7-methyl-3-(3-trifluoromethyl)-7,8-dihydro-6H-cinnolines-5-ketone, 7-methyl-3-(3-trifluoromethyl)-5; 6,7,8-tetrahydrochysene cinnolines-5-alcohol; 7-methyl-3-(3-trifluoromethyl) cinnolines-5-alcohol, 7-methyl isophthalic acid-oxo-3-(3-trifluoromethyl)-5,6; 7,8-tetrahydrochysene cinnolines-5-alcohol, 5-glycyl oxygen base-7-methyl-3-(3-trifluoromethyl)-5; 6; 7,8-tetrahydrochysene cinnolines, 5-(L-alanyl oxygen base)-7-methyl-3-(3-trifluoromethyl)-5; 6; 7,8-tetrahydrochysene cinnolines, 5-(L-valyl oxygen base)-7-methyl-3-(3-trifluoromethyl)-5; 6; 7,8-tetrahydrochysene cinnolines, 5-(L-α-Gu Anxianji oxygen base)-7-methyl-3-(3-trifluoromethyl)-5; 6; 7,8-tetrahydrochysene cinnolines, or the like.
In the used 3-phenyl-cinnolines analogue of the present invention, when compound has asymmetric carbon and provides with the form of optically active compound or raceme, comprise its all such optically active compounds, its mixture and its racemies.In addition, comprise its hydrate or solvate equally.
In addition, steric isomer and its mixture based on imido base key (C=N) all is included in above-mentioned 3-phenyl-cinnolines analogue.
The example of the acceptable salt of physiology of the present invention comprises: mineral acid is hydrochloric acid, vitriolic salt for example, or the like; Organic acid is the salt of acetate, succsinic acid, fumaric acid, toxilic acid, citric acid, phenylformic acid, tartrate, methylsulfonic acid, tosic acid for example, or the like.Can easily prepare its salt by the salifiable reaction of conventional shape.
As antineoplastic agent of the present invention, comprise 3-phenyl-cinnolines analogue, it can be by means of body physiological condition (for example exist " Development of Pharmaceuticals; Vol.7, Molecular Design ", Hirokawa Publishing Co., Tokyo, 1990, the physiological condition of describing in p.163-198) the enzymatic application down or the mode of gastric juice, the conversion that causes by oxidizing reaction, reduction reaction, hydrolysis reaction or the like demonstrates anti-tumor activity.
Oral or parenteral gives antineoplastic agent of the present invention with following form, the dosage form of suspension, milk sap, injection, inhalation, tablet, pill, granule, microgranules, powder, capsule, the liquid preparation that orally uses, suppository, the liquid preparation that uses through skin, the paster that uses through skin, ointment, the liquid preparation that uses through mucous membrane, paster of using through mucous membrane or the like for example, form with 3-phenyl-cinnolines analogue or the acceptable salt of its physiology gives separately, or gives with the form with vehicle or carrier mixed preparation.Additive for example vehicle or carrier is selected from pharmaceutically acceptable material, and its type and composition are by considering that route of administration or medication are determined.For example, under the situation of using injection, usually preferred sodium-chlor, carbohydrate be glucose, mannitol or the like for example.Under the situation of using oral preparations, preferred starch, lactose, crystalline cellulose, Magnesium Stearate or the like.If necessary, auxiliary agent is subsidiary, stablizer, wetting agent or emulsifying agent, damping fluid and other normally used additive for example, can be with its optional being included in the above-mentioned preparation.
The amount of the compound in preparation of the present invention changes according to preparation, yet, 0.1-100% weight percentage normally, preferred 1-98% weight percentage.For example, under the situation of using injection, by weight, active ingredient can contain 0.1-30% usually, preferred 1-10%.Under the situation of oral preparations, the form as tablet, capsule, powder, granule, liquid preparation, dry syrup or the like is used with additive.Capsule, tablet, granule or powder by weight, contain 5-100% usually, the active ingredient of preferred 25-98%.
Dosage level can be determined according to age, sex, body weight, symptom and therapeutic purpose, for administered parenterally, therapeutic dose is generally the 0.001-100 mg/kg/day, and for oral administration, be the 0.01-500 mg/kg/day, preferred 0.1-100 mg/kg/day once gives or is divided into 2 to 4 administrations.
3-phenyl-cinnolines analogue that the present invention uses can prepare by a kind of method, for example, according to the method for in non-patent literature 3 above, describing, and will show among the embodiment below and synthesize embodiment, yet the preparation method is not particularly limited to these embodiment.
Particularly, for example, a kind of compound, acetophenone derivs by the represented alpha-halogen replacement of following general formula (6), can be from purchases such as Tokyo Kasei Kogyo Co.Ltd., or can also obtain by the following method: acetophenone derivs commercial or that be easy to obtain according to the production method of known reference, in room temperature to reflux temperature, use N-halo succinimide or use for example bromine of halogen separately, iodine or the like, or use salt for example pyridine bromide perbromide (pyridinium bromide perbromide) as halide reagent, at reaction solvent toluene for example, in tetrahydrofuran (THF) or the like, be easy to it is carried out halo.
Wherein E is a halogen atom; X and X ' have identical implication hereinbefore.
As for being used for preparation at 1 of the compound (wherein L is W-C-W ') of above-mentioned general formula (1), 3-cycloalkanes diketone, for example 1,3-diacetylmethane or 1,3-suberane diketone can be bought from Sigma-Aldrich Co.Further, although by 1 of the expression of general formula (7) hereinafter, compound among the hydroresorcinol derivative can commercially be bought, but if necessary, can also prepare according to the diagram method in the following reaction scheme: the mixture of methyl ethylene ketone derivatives (8) and malonic ester derivative (9), in room temperature to reflux temperature, at solvent for example in water, methyl alcohol, ethanol or the like, metal alkoxide for example sodium methylate, sodium ethylate or the like in the presence of, or oxyhydroxide for example sodium hydroxide, potassium hydroxide or the like in the presence of, react.
Wherein R represents low alkyl group; W has and above identical implication with W '.
Perhaps, according to following diagram, can catalyzer for example platinum, palladium or the like in the presence of, at organic solvent for example in methyl alcohol, tetrahydrofuran (THF) or the like, the hydrogenation by resorcinol derivatives (10) prepares.
Wherein W has implication same as above.
Can be used for preparing the 5-azepine-hydroresorcinol derivative (7b) of general formula (1) compound (wherein L is N-W), can be according at Archiv der Pharmazie, 1967, No.300, the method for describing in p.91-94 prepares.Promptly, target compound (7b) can obtain as follows: by the glycine derivative of general formula (11) expression and bromoacetophenone in room temperature to reflux temperature, at organic solvent for example in ethanol, methyl-sulphoxide, tetrahydrofuran (THF) or the like, alkali for example sodium bicarbonate, salt of wormwood, cesium carbonate or the like in the presence of react, obtain keto ester (12).Keto ester (12) is at organic solvent for example in ethanol, the trimethyl carbinol or the methyl-sulphoxide then, 0 ℃ to room temperature, alkali for example sodium methylate, potassium tert.-butoxide, sodium hydride or the like in the presence of react.
Wherein R is a low alkyl group, and W has and above identical implication.
A kind of above 1, the compound of 3-cycloalkanes derovatives and above-mentioned general formula (6) in room temperature to reflux temperature, at organic solvent for example in methyl-sulphoxide, methylene dichloride, chloroform, tetrahydrofuran (THF), methyl alcohol, ethanol or the like, and alkali for example sodium hydride, sodium hydroxide, potassium hydroxide, salt of wormwood, cesium carbonate, sodium methylate, sodium ethylate or the like in the presence of react, obtain compound by general formula (13) expression.
K wherein, L, M, X and X ' have implication same as above.
By the compound of general formula (13) expression at organic solvent for example in methyl alcohol, ethanol or the like, alkali for example triethylamine, pyridine or the like in the presence of, in room temperature to the reflux temperature of used organic solvent, react with hydrazine hydrochloride, obtain by 4 of general formula (14) expression, 6,7,8-six hydrogen-1H-cinnolines-5-ketone derivatives.
K wherein, L, M, X and K ' have implication same as above.
Further, the compound of representing by general formula (1a) below this paper, can be under the condition of reflux, at basic solvent pyridine for example, in triethylamine or the like, atmospheric oxidation by described compound (14) obtains, or under the condition of reflux, at organic solvent methyl alcohol for example, ethanol, in tetrahydrofuran (THF) or its mixed solvent, at metal catalyst palladium for example, under the existence of platinum or the like, oxidation by compound (14) obtains, or by with oxygenant cerium (IV) for example, ammonium nitrate, 2,3-two chloro-5,6-dicyano-para benzoquinone or the like is handled compound (14) and is obtained.
K wherein, L, M, X and X ' have implication same as above.
Further, by the compound of general formula (1) expression, wherein J is H-C-OH, and n and n ' are 0, can be by for example sodium borohydride, lithium aluminum hydride, three tert.-butoxy lithium aluminum hydrides or the like react and obtain by the compound of general formula (1a) expression and reductive agent; Or at organic solvent for example in tetrahydrofuran (THF), methyl alcohol, ethanol or the like, in ice-cooled temperature to room temperature, with alkyl metal cpd for example lithium methide, sec.-propyl bromination magnesium or the like reaction obtain.
Further, the compound that has the general formula (1) of various Y groups can be by the preparation of following method: at organic solvent for example methylene dichloride, tetrahydrofuran (THF), N, in dinethylformamide, ethyl acetate or the like, exist or do not exist organic bases for example under the condition of pyridine, triethylamine or the like, by for example reaction of Acetyl Chloride 98Min., propionyl bromide or the like of chloride of acid; Or in the presence of dimethyl aminopyridine, use condensing agent for example dicyclohexylcarbodiimide, N-ethyl-N '-3-dimethylaminopropyl carbodiimide or the like, by for example reaction of N-tertbutyloxycarbonyl-L-Xie Ansuan, N-carbobenzoxy-(Cbz)-D-proline(Pro) or the like of protected amino acid; And, for example use trifluoromethanesulfonic acid, hydrochloric acid, hydrogenolysis or the like to remove amino acid whose protecting group according to a kind of ordinary method; Or at organic solvent N for example, in dinethylformamide, methyl-sulphoxide, tetrahydrofuran (THF) or the like, at alkali for example potassium tert.-butoxide, sodium hydride and N, under the existence of N-diisopropylethylamine, by for example reaction of methyl iodide, bromotoluene or the like of haloalkane.
Further, by the N-oxide compound (n and/or n '=1) of general formula (1) expression, can by oxygenant for example the compound (wherein n and n ' they are 0) of metachloroperbenzoic acid, peracetic acid or the like and general formula (1) and for example react in methylene dichloride, chloroform or the like at organic solvent and obtain.
Compound by above-mentioned general formula (4) expression, can also obtain by following method: have or do not exist organic solvent for example acetate, N, under the condition of dinethylformamide or the like, in room temperature to reflux temperature, and if necessary, use alkali for example collidine, triethylamine, 1,8-diazabicyclo [5.4.0]-7-undecylene or the like is by the compound (wherein each of W and W ' is hydrogen atom) and for example cupric bromide, lithium chloride, iodine or the like reaction of halogenating agent by general formula (1a) expression.Further, by the compound of general formula (4) expression, can directly carry out oxidizing reaction by the compound (wherein each of W and W ' is hydrogen atom) that makes general formula (1a) expression and obtain hereinbefore.
In addition, various derivatives can prepare by the conventional conversion reaction that makes the compound that obtains like this carry out phenolic hydroxyl group.For example; at organic solvent methylene dichloride for example; tetrahydrofuran (THF); N; dinethylformamide; in ethyl acetate or the like; there is or do not exist for example pyridine of organic bases; under the condition of triethylamine or the like; by chloride of acid Acetyl Chloride 98Min. for example; various carboxyl groups are introduced in the reaction of propionyl bromide or the like; or at organic solvent N for example; dinethylformamide; methyl-sulphoxide; in tetrahydrofuran (THF) or the like; at alkali potassium tert.-butoxide for example; sodium hydride; N; under the existence of N-diisopropylethylamine or the like, by haloalkane methyl iodide for example; various alkyl are introduced in the reaction of bromotoluene or the like.
Further, derivative with imido base key can also obtain by following method: at organic solvent for example in methyl alcohol, ethanol or the like, organic bases for example pyridine, triethylamine or the like in the presence of, in room temperature to reflux temperature, with general formula (14) or (1a) compound of expression with for example for example oxammonium hydrochloride, methoxy amine hydrochlorate, O-ethyl oxammonium hydrochloride or the like the heating of hydrazine hydrochloride, ethyl hydrazine hydrochloride and methylhydrazine hydrochloride or low-grade alkyl azanol of low alkyl group hydrazine, if necessary, make it carry out oxidizing reaction.
In order to separate and the purification of target compound the reaction mixture that obtains from the various preparation methods by above, the use ordinary method that can depend on the circumstances comprises solvent extraction, concentrates distillation, recrystallization, chromatography or the like.
The present invention includes inhibition of cell proliferation, this inhibition of cell proliferation comprises by acceptable salt on the 3-phenyl-cinnolines analogue of above-mentioned general formula (1), general formula (2), general formula (3), general formula (4) or general formula (5) expression or its physiology as active ingredient.Be similar to compound, can be used as inhibition of cell proliferation, antineoplastic agent by the compound of above-mentioned general formula (1), general formula (2), general formula (3), general formula (4) or general formula (5) expression, and same and top identical of particular compound.
The present invention further comprises by acceptable salt on the 3-phenyl-cinnolines analogue of above general formula (1) or (2) expression or its physiology, does not comprise that wherein Z is the compound of Sauerstoffatom.That is, the present invention includes 3-phenyl-cinnolines analogue of representing by following general formula (1) or (2):
Wherein J is A-C-B (C is a carbon atom); A is that (O is a Sauerstoffatom to the O-Y group; Y is a hydrogen atom, can choose the low alkyl group that is replaced by phenyl wantonly, lower acyl or can protected amino-acid residue); B is a hydrogen atom, low alkyl group, or form the imino-of carbonyl or replacement with A; K is (CH
2)
qL is N-W (N is a nitrogen-atoms) or W-C-W ' (C is a carbon atom); Each is low alkyl group independently for W and W ', and it can have the substituting group that is selected from hydroxyl, lower alkoxy and phenyl, phenyl, carboxyl, lower alkoxycarbonyl or hydrogen atom; M is (CH
2)
mOr J-K-L-M is C (O-Y)=CH-C (W)-CH (Y has identical implication with W hereinbefore); Z is N-Q (Q is amino, low-grade alkyl amino, hydroxyl or lower alkoxy); Each is low alkyl group independently for X and X ', lower alkoxycarbonyl, rudimentary amido, lower alkoxy, halogenated lower alkyl, nitro, cyano group, halogen atom or hydrogen atom; Each is 0 to 3 integer independently for m and q; And each is 0 or 1 independently for n and n ', or acceptable salt on its physiology.
Further, the present invention includes 3-phenyl-cinnolines analogue or its physiologically acceptable salt, do not comprise by the represented compound of general formula (5) (wherein Z is a Sauerstoffatom) by general formula (3), general formula (4) or general formula (5) expression.
Particularly, except by general formula (2) or the represented compound (wherein Z is a Sauerstoffatom) of general formula (5), can comprise the compound that all above-mentioned general formulas (1) are given an example to (5).
Embodiment
The present invention can typically be illustrated with embodiment, test example and reference example, yet the present invention is not limited.
In the present invention, ESI is the abbreviation of " electrospray ionization ", and FAB is the abbreviation of " fast atom bombardment ", and each all is the ioning method that is used for molecular weight determination in the mass spectrum.
The hydrogen nuclei Magnetic Resonance Spectrum (
1H-NMR) be by being that the δ of benchmark represents with TMS (tetramethylsilane).
Embodiment 1
7-phenyl-3-(3-trifluoromethyl)-7, the synthetic 7-phenyl-3-(3-trifluoromethyl)-4 that will in reference example 2, obtain of 8-dihydro-6H-cinnolines-5-ketone, 6,7, pyridine (5 milliliters) solution of 8-tetrahydrochysene-1H-cinnolines-5-ketone stirred 3 days down at 70 ℃.To use silica gel column chromatography (hexane/ethyl acetate=3/1) to carry out purifying by the reaction liquid concentrated resistates that obtains under reduced pressure, obtain yellow thick product, by suspension method (hexane/ethyl acetate=3ml/0.5ml) be further purified, obtain target compound (124.0mg, 48.9%, in step 2).
1H-NMR (200MHzFT, TMS, CDCl
3) 2.93-3.23 (2H, complicated peak), 3.51-3.75 (2H, complicated peak), 3.76-3.97 (1H, m), 7.20-7.49 (5H, m), 7.70 (1H, t, J=7.8Hz), 7.80 (1H, d, J=7.8Hz), 8.31-8.42 (1H, m), 8.46 (1H, brs) MS (ESI)
m/z 369[M+H]
+
Embodiment 2
5-oxo-3-(3-trifluoromethyl)-7,8-dihydro-6H-cinnolines-7-carboxylic acid ethyl ester synthetic
Except replacing 5-phenyl-1 with the 3-hydroxyl-5-oxo-hexamethylene that obtains in the reference example 3-3-olefinic carboxylic acid ethyl ester, beyond the hydroresorcinol, by being similar to the reaction in the reference example 1, then carry out, obtain target compound according to the method that is similar among reference example 2 and the embodiment 1.
1H-NMR(200MHzFT,TMS,CDCl
3)1.26(3H,dt,J=1.8,7.1Hz),3.04(2H,d,J=6.4Hz),3.62-3.87(2H,m),4.19(1H,q,J=7.1Hz),7.69(1H,t,J=7.7Hz),7.80(1H,d,J=8.0Hz),8.31(1H,s),8.34(1H,d,J=7.7Hz),8.44(1H,s)
MS(ESI)
m/z 365[M+H]
+
Embodiment 3
5-hydroxyl-3-(3-three fluoro-aminomethyl phenyls)-5,6,7,8-tetrahydrochysene cinnolines-7-carboxylic acid ethyl ester synthetic
To the 5-oxo-3-that in embodiment 2, obtains (3-three fluoro-aminomethyl phenyls)-7, (100 milligrams of 8-dihydros-6H-cinnolines-7-carboxylic acid, ethyl ester, 0.274mmol) ethanolic soln (0.5 milliliter) in add sodium borohydride (10.4 milligrams 0.274mmol), were at room temperature stirred 1 hour.After reaction is finished, with 1N aqueous potassium hydrogen sulfate (1mL) cancellation reaction liquid, extract with ethyl acetate (3ml), then use dried over sodium sulfate, the filtration drying agent under reduced pressure concentrates organic layer, uses silica gel column chromatography (hexane/ethyl acetate=1/1 is to 1/2) purifying resistates, obtain target compound (65mg, 64.8%) light yellow solid.
1H-NMR (200MHzFT, TMS, CDCl
3) 1.30 (3H, t, J=7.1Hz), 2.11 (1H, ddd, J=8.2,9.5,13.5Hz), 2.56 (1H, dq, J=3.1,13.5Hz), (3.00-3.18 2H, complicated peak), and 3.38-3.63 (2H, m), 4.21 (2H, q, J=7.1Hz), 4.92 (1H, brt, J=7.2Hz), 7.65 (1H, t, J=7.7Hz), 7.75 (1H, brd, J=7.8Hz), 8.09 (1H, s), 8.32 (1H, d, J=7.7Hz), 8.37 (1H, brs)
MS(ESI)
m/z 367[M+H]
+
Embodiment 4
5-hydroxyl-3-(3-three fluoro-aminomethyl phenyls)-5,6,7,8-tetrahydrochysene cinnolines-7-carboxylic acid synthetic
5-hydroxyl-the 3-that will in embodiment 3, obtain (3-trifluoromethyl)-5,6,7, and 8-tetrahydrochysene cinnolines-7-carboxylic acid ethyl ester (60 milligrams, 0.164mmol) be dissolved in the diox (1ml), the dense HCl solution and the stirring that then add 0.1 milliliter are spent the night.Reaction liquid is concentrated, then neutralize with sodium bicarbonate aqueous solution, use the 1N sodium pyrosulfate aqueous solution to produce slightly acidic, use ethyl acetate extraction, use anhydrous sodium sulfate drying, filter, under reduced pressure the organic layer that will obtain like this concentrates, and use silica gel column chromatography (methylene chloride=10/1) purifying resistates, obtain target compound (3mg, 5.4%).
MS(ESI)
m/z 339[M+H]
+
Embodiment 5
5-oxo-3-(3-three fluoro-aminomethyl phenyls)-7,8-dihydro-6H-cinnolines-7-carboxylic acid synthetic
According to the method that is similar to embodiment 4, by the 5-oxo-3-(3-trifluoromethyl)-7 that obtains among the embodiment 2, and 8-dihydro-6H-cinnolines-7-carboxylic acid ethyl ester (100 milligrams, acid hydrolysis 0.274mmol), obtain target compound (67.7 milligrams, 73.5%).
MS(ESI)
m/z 337[M+H]
+
Embodiment 6
7-methyl-3-(3-three fluoro-aminomethyl phenyls)-5,6,7,8-tetrahydrochysene cinnolines-5-alcohol synthetic
According to the method that is similar to embodiment 3, by the 5-oxo-3-(3-trifluoromethyl)-7 that obtains in the Processing Example 66, (1g 3.28mmol), obtains target compound (917.9 milligrams, 90.9%) white solid to 8-dihydro-6H-cinnolines.Measure by HPLC, find that the ratio of its cis/trans is approximately 9/1.
1H-NMR(200MHzFT,TMS,CDCl
3)1.22(3H,d,J=6.6Hz),1.51(1H,q,J=12.2Hz),1.88-2.44(1H,m),2.24-2.42(1H,m),2.73(1H,ddd,J=1.1,11.7,18.0Hz),3.41(1H,ddd,J=1.8,5.2,17.8Hz),4.90(1H,q,J=5.8,11.3Hz),7.62(1H,t,J=7.7Hz),7.73(1H,d,J=7.8Hz),8.14(1H,d,J=1.1Hz),8.29(1H,d,J=8.0Hz),8.34(1H,s)MS(ESI)
m/z 309[M+H]
+
Embodiment 7
7-methyl-3-(3-three fluoro-aminomethyl phenyls)-5,6,7,8-tetrahydrochysene cinnolines-5-alcohol synthetic
To the 7-methyl-3-that in embodiment 6, obtains (3-trifluoromethyl)-5,6,7, (92.5 milligrams of 8-tetrahydrochysene-cinnolines-5-alcohol, 0.3mmol) benzole soln (16 milliliters) in add triphenylphosphine (480 milligrams, 1.47mmol), the 4-nitrobenzoic acid (221 milligrams, 1.32mmol) and (0.23 milliliter of azoethane dicarboxylic ester, 1.47mmol), and at room temperature stirred 1 hour.Use silica gel column chromatography (hexane/ethyl acetate=2: 1) with the reaction liquid purifying, obtain trans-(±)-7-methyl-5-(4-nitrophenyl ketonic oxygen base)-3-(3-trifluoromethyl)-5,6,7,8-tetrahydrochysene cinnolines.The compound that obtains like this is dissolved in the methyl alcohol (5 milliliters), to wherein adding 2N NaOH solution (1 milliliter), then at room temperature reacted 1 hour, and added distilled water (2 milliliters) and ethyl acetate (5 milliliters) and be used to extract and wash by extract the organic layer that obtains with saturated salt solution.After using anhydrous sodium sulfate drying, the concentrating under reduced pressure organic layer then uses silica gel column chromatography (hexane/ethyl acetate=3/1) purifying resistates, obtains target compound (45 milligrams, 48.7%) white solid.Measure by HPLC, find that the ratio of its cis/trans is approximately 7/93.
1H-NMR (200MHzFT, TMS, CDCl
3) 1.20 (3H, d, J=6.7Hz), 1.78 (1H, ddd, J=4.5,10.7,14.OHz), and 2.01-2.15 (1H, m), 2.20-2.45 (1H, m), 2.71 (1H, dd, J=10.1,17.6Hz), 3.41 (1H, ddd, J=1.3,4.9,17.6Hz), 4.97 (1H, t, J=4.3Hz), 7.63 (1H, t, J=7.7Hz), 7.73 (1H, d, J=7.7Hz), 7.92 (1H, s), 8.25-8.36 (2H, complicated peak)
MS(ESI)
m/z 309[M+H]
+
Embodiment 8
Cis-5-(N-(tert.-butoxy-carbonyl)-L-prolyl } oxygen base-7-methyl-3-(3-three fluoro-aminomethyl phenyls)-5,6,7,8-tetrahydrochysene cinnolines synthetic
To (21 milligrams of N-(tertbutyloxycarbonyl)-L-proline(Pro), 0.098mmol), 7-methyl-3-(3-trifluoromethyl)-5,6,7,8-tetrahydrochysene cinnolines-5-alcohol (23.4 milligrams 0.076mmol) and N, add (24 milligrams of dicyclohexylcarbodiimide in the tetrahydrofuran solution of N-dimethyl aminopyridine (catalytic amount) (0.5 milliliter), 0.114mmol), at room temperature stir and spend the night.In reaction liquid, add hexane/ethyl acetate (1/1,1ml), then be coated on the silicagel column of diameter 10mm, long 15mm, use eluent ethyl acetate, the concentrating under reduced pressure eluting liquid, (0.5mm is thick to use preparation thin layer TLC, 20cm * 20cm, 2, hexane/ethyl acetate=2/1) purifying resistates obtains the diastereomer of two kinds of target compounds: low-polarity constituents (17.4mg) and high polar compound (17.5mg).Also obtain the non-enantiomer mixture of the 5.1mg that constitutes by trans material simultaneously.
MS(ESI)
m/z 506[M+H]
+
Embodiment 9
Cis-(-)-7-methyl-3-(3-trifluoromethyl)-5,6,7,8-tetrahydrochysene-cinnolines-5-alcohol synthetic
In embodiment 8, obtain, as adding the 3N NaOH aqueous solution (3) in the methanol solution (1mL) of the cis diastereomer of low-polarity constituents, and at room temperature stirred 3.25 hours.The concentrating under reduced pressure reaction liquid, and the resistates that will obtain like this is coated on the silicagel column of diameter 10mm, long 15mm, then use eluent ethyl acetate, the concentrating under reduced pressure eluting liquid, and (0.5mm is thick, 20cm * 10cm, 2 to use preparation thin layer TLC, hexane/ethyl acetate=1/1) purifying resistates obtains target compound (10.1mg)
MS(ESI)
m/z 309[M+H]
+
[α]
D 25-131 ° (c0.51, methyl alcohol)
Embodiment 10
Cis-(+)-7-methyl-3-(3-trifluoromethyl)-5,6,7,8-tetrahydrochysene-cinnolines-5-alcohol synthetic
According to the method that is similar to embodiment 9, use cis diastereomer that obtain, high polar compound (17.5mg) among the embodiment 8, obtain target compound (9.8mg).
MS(ESI)
m/z 309[M+H]
+
[α]
D 25+ 135 ° (c0.49, methyl alcohol)
Embodiment 11
5-acetoxyl group-7-methyl-3 (3-trifluoromethyl)-5,6,7,8-tetrahydrochysene-cinnolines synthetic
Under ice-cooled, to the 7-methyl-3-that in embodiment 6, obtains (3-trifluoromethyl)-5,6,7,8-tetrahydrochysene-cinnolines-5-alcohol (adds (0.027 milliliter of diacetyl oxide among the 61.6mg, pyridine solution 0.2mmol) (1 milliliter), 0.24mmol), and reaction was at room temperature carried out 2 hours.The concentrating under reduced pressure reaction soln, the residue purified of then using silica gel column chromatography (hexane/ethyl acetate=3/1) to obtain like this obtains target compound (57.6mg, 82.3%).
1H-NMR(200MHzFT,TMS,CDCl
3)1.23(3H,d,J=6.6Hz),1.51(1H,q,J=12.3Hz),2.07-2.27(1H,m),2.24(3H,s),2.32-2.46(1H,m),2.80(1H,ddd,J=1.4,11.5,17.8Hz),3.44(1H,ddd,J=1.8,5.1,17.9Hz),6.03(1H,dd,J=6.1,10.8Hz),7.65(1H,t,J=7.7Hz),7.68(1H,s),7.75(1H,d,J=7.6Hz),8.23(1H,d,J=7.7Hz),8.33(1H,brs)
MS(ESI)
m/z 351[M+H]
+,291[M+H-CH
3COOH]
+
Embodiment 12
7-methyl isophthalic acid-oxo-3-(3-trifluoromethyl)-7,8-dihydro-6H-cinnolines-5-alcohol synthetic
Under ice-cooled, to the 7-methyl-3-that in embodiment 6, obtains (3-trifluoromethyl)-5,6,7, (90mg adds 3-chlorine peroxybenzoic acid (122.5mg to 8-tetrahydrochysene-cinnolines-5-alcohol in dichloromethane solution 0.294mmol), 0.71mmol), and reaction was carried out 2 hours.Concentrated solvent, then adding 3% wet chemical (1mL) and ethyl acetate (3mL) extracts, use anhydrous sodium sulfate drying, removal of solvent under reduced pressure, and the residue purified of using silica gel column chromatography (hexane/ethyl acetate=1/1 is to 0/1) to obtain like this, obtain target compound (49.2mg, 51.6%).
1H-NMR (200MHzFT, TMS, CDCl
3) 1.22 (3H, d, J=6.6Hz), 1.51 (1H, dd, J=12.3Hz), (1.66-2.20 2H, complicated peak), 2.21-2.36 (1H, m) 2.40 (1H, dd, J=11.3,19.3Hz), 3.24 (1H, dd, J=5.3,19.3Hz), 4.88 (1H, dd, J=5.5,11.4Hz), 7.60 (1H, t, J=7.8Hz), 7.69 (1H, d, J=7.7Hz), 8.19 (1H.d, J=7.8Hz), 8.25 (1H, brs)
MS(ESI)
m/z 325[M+H]
+
Embodiment 13
5-oxo-1-oxygen base-3-(3-trifluoromethyl)-7,8-dihydro-6H-cinnolines synthetic
According to the method that is similar to embodiment 12, by the 5-oxo-3-(3-trifluoromethyl)-7 that obtains in the Processing Example 66, (306mg 1mmol), obtains target compound (124 milligrams, 38%) to 8-dihydro-6H-cinnolines.
MS(ESI)
m/z 323[M+H]
+
Embodiment 14
7-methylol-3-(3-trifluoromethyl)-5,6,7,8-tetrahydrochysene-cinnolines-5-alcohol synthetic
Under-40 ℃, (14.5 milligrams of lithium aluminium hydride in tetrahydrofuran (THF) (1 milliliter), 0.38mmol) be added in the 5-oxo-3-(3-trifluoromethyl)-7 that obtains among the embodiment 2 in the suspension, (92.8 milligrams of 8-dihydros-6H-cinnolines-7-carboxylic acid ethyl ester, 0.25mmol), then stirred as it is 1 hour, and elevated temperature gradually, until room temperature.Add ethyl acetate (3 milliliters) and 1N HCl solution (0.5 milliliter) quencher reaction, then further add distilled water (2 milliliters) and extract.With the organic layer of anhydrous sodium sulfate drying by obtaining with the saturated salt solution washing, filtration drying agent then, concentrating under reduced pressure organic layer, and the residue purified of using silica gel column chromatography (methylene chloride=10/1) to obtain like this, obtain target compound (29.9mg, 36.3%).
MS(ESI)
m/z 325[M+H]
+
Embodiment 15
3-(3-cyano-phenyl)-7-methyl-7,8-dihydro-6H-cinnolines-5-ketone synthetic
According to the method that is similar to reference example 1, use 2-bromo-3 '-cyanoacetophenone replace 2-bromo-3 '-trifluoromethyl acetophenone, 5-methyl isophthalic acid, hydroresorcinol replaces 5-phenyl-1, hydroresorcinol, then handle the product that obtains like this, obtain target compound according to the method that is similar to reference example 2 and embodiment 1.
MS(ESI)
m/z 264[M+H]
+
Embodiment 16
3-(3-cyano-phenyl)-7-methyl-5,6,7,8-tetrahydrochysene cinnolines-5-alcohol synthetic
According to the method that is similar to reference example 3, the 3-that obtains in the Processing Example 15 (3-cyano-phenyl)-7-methyl-7,8-dihydro-6H-cinnolines-5-ketone obtains target compound.
MS(ESI)
m/z 266[M+H]
+
Embodiment 17
7,7-dimethyl-3-(3-trifluoromethyl)-5,6,7,8-tetrahydrochysene-cinnolines-5-alcohol synthetic
Handle according to the method that is similar to reference example 1, use 5,5-dimethyl-1, hydroresorcinol replaces 5-phenyl-1, hydroresorcinol is then handled the product that obtains like this according to the method that is similar among reference example 2, embodiment 1 and the embodiment 3, obtains target compound.
MS(ESI)
m/z 323[M+H]
+
Embodiment 18
3-(3-trifluoromethyl)-5,6,7,8-tetrahydrochysene cinnolines-5-alcohol synthetic
According to the method that is similar to reference example 1, use hydroresorcinol to replace 5-phenyl-hydroresorcinol, then handle the product that obtains like this and obtain target compound according to the method among reference example 2, embodiment 1 and the embodiment 3 of being similar to.
MS(ESI)
m/z 295[M+H]
+
Embodiment 19
3-(3-bromophenyl)-7-methyl-7,8-dihydro-6H-cinnolines-5-ketone synthetic
According to the method that is similar to reference example 1, use 2,3 '-the dibromobenzene ethyl ketone replace 2-bromo-3 '-trifluoromethyl acetophenone, 5-methyl isophthalic acid, hydroresorcinol replaces 5-phenyl-1, hydroresorcinol, then handle the product that obtains like this, obtain target compound according to the method that is similar to reference example 2 and embodiment 1.
MS(ESI)
m/z 317,319[M+H]
+
Embodiment 20
7-methyl-3-(3-nitrophenyl)-7,8-dihydro-6H-cinnolines-5-ketone synthetic
According to the method that is similar to reference example 1, use 2-bromo-3 '-nitro-acetophenone replace 2-bromo-3 '-trifluoromethyl acetophenone, 5-methyl isophthalic acid, hydroresorcinol replaces 5-phenyl-1, hydroresorcinol, then handle the product that obtains like this, obtain target compound according to the method that is similar to reference example 2 and embodiment 1.
MS(ESI)
m/z 284[M+H]
+
Embodiment 21
7-methyl-3-(3-tolyl)-7,8-dihydro-6H-cinnolines-5-ketone synthetic
According to the method that is similar to reference example 1, use 2-bromo-3 '-methyl acetophenone replace 2-bromo-3 '-trifluoromethyl acetophenone, 5-methyl isophthalic acid, hydroresorcinol replaces 5-phenyl-1, hydroresorcinol, then handle the product that obtains like this, obtain target compound according to the method that is similar to reference example 2 and embodiment 1.
MS(ESI)
m/z 253[M+H]
+
Embodiment 22
3-(3-methoxycarbonyl-phenyl)-7-methyl-7,8-dihydro-6H-cinnolines-5-ketone synthetic
According to the method that is similar to reference example 1; use 3-(2 '-acetyl bromide) benzoic acid methyl ester replace 2-bromo-3 '-trifluoromethyl acetophenone, 5-methyl isophthalic acid; hydroresorcinol replaces 5-phenyl-1; hydroresorcinol; then handle the product that obtains like this, obtain target compound according to the method that is similar to reference example 2 and embodiment 1.
MS(ESI)
m/z 297[M+H]
+
Embodiment 23
3-(3-acetylamino phenyl)-7-methyl-7,8-dihydro-6H-cinnolines-5-ketone synthetic
According to the method that is similar to reference example 1; use 3-(2 '-acetyl bromide) Acetanilide replace 2-bromo-3 '-trifluoromethyl acetophenone, 5-methyl isophthalic acid; hydroresorcinol replaces 5-phenyl-1; hydroresorcinol; then handle the product that obtains like this, obtain target compound according to the method that is similar to reference example 2 and embodiment 1.
MS(ESI)
m/z 296[M+H]
+
Embodiment 24
3-(3-fluorophenyl)-7-methyl-7,8-dihydro-6H-cinnolines-5-ketone synthetic
According to the method that is similar to reference example 1, use 2-bromo-3 '-fluoro acetophenone replace 2-bromo-3 '-trifluoromethyl acetophenone, 5-methyl isophthalic acid, hydroresorcinol replaces 5-phenyl-1, hydroresorcinol, then handle the product that obtains like this, obtain target compound according to the method that is similar to reference example 2 and embodiment 1.
MS(ESI)
m/z 257[M+H]
+
Embodiment 25
3-(3-p-methoxy-phenyl)-7-methyl-7,8-dihydro-6H-cinnolines-5-ketone synthetic
According to the method that is similar to reference example 1, use 2-bromo-3 '-methoxyacetophenone replace 2-bromo-3 '-trifluoromethyl acetophenone, 5-methyl isophthalic acid, hydroresorcinol replaces 5-phenyl-1, hydroresorcinol, then handle the product that obtains like this, obtain target compound according to the method that is similar to reference example 2 and embodiment 1.
1H-NMR (200MHzFT, TMS, CDCl
3) 1.27 (3H, d, J=6.2Hz), 2.37-2.59 (2H, complicated peak), (2.78-3.14 2H, complicated peak), and 3.51-3.67 (1H, m), 3.92 (3H, s), 7.07 (1H, ddd, J=1.0,2.6,8.2Hz), 7.45 (1H, t, J=8.0Hz), 7.66 (1H, ddd, J=1.1,1.5,7.7Hz), 7.78 (1H, dd, J=1.6,2.6Hz), 8.25 (1H, s)
MS(ESI)
m/z 269[M+H]
+
Embodiment 26
7-benzyl-3-(3-trifluoromethyl)-7,8-dihydro-6H-pyrido [3,4-c]-pyridazin-3-one synthetic
According to the method that is similar to reference example 1, use 1-benzyl-5-hydroxyl-1,6-dihydro-2H-pyridine-3-ketone replaces 5-phenyl-hydroresorcinol, then handle the product that obtains like this, obtain target compound according to the method that is similar to reference example 2 and embodiment 1.
MS(ESI)
m/z 384[M+H]
+
Embodiment 27
7-(2-hydroxyl-2-propyl group)-3-(3-trifluoromethyl)-5,6,7,8-tetrahydrochysene-cinnolines-5-alcohol synthetic
With the 5-hydroxyl-3-(3-trifluoromethyl)-5 that obtains among the embodiment 3,6,7, (5 milligrams of 8-tetrahydrochysene cinnolines-7-carboxylic acid ethyl ester, 0.01mmol) tetrahydrofuran solution (1 milliliter) be cooled to-20 ℃, then add the 3N methylmagnesium-bromide tetrahydrofuran solution (0.3 milliliter, 0.9mmol), stirring is spent the night, simultaneously elevated temperature.In reaction liquid, add the ethyl acetate (3mL) and the sodium pyrosulfate aqueous solution (1mL), and aftercut, with the organic layer that anhydrous sodium sulfate drying obtains like this, the organic layer that filtration drying agent and concentrating under reduced pressure obtain like this, obtain target compound (4.5mg, 93.9%).
1H-NMR(200MHzFT,TMS,CDCl
3)1.21(3H,s),1.24(3H,s),1.58-1.74(1H,m),1.94-2.14(1H,m),2.42-2.56(1H,m),3.03(1H,dd,J=11.0,17.6Hz),3.41(1H,dd,J=5.2,17.6Hz),4.88(1H,dd,J=5.3,10.4Hz),7.62(1H,t,J=7.7Hz),7.73(1H,d,J=7.7Hz),8.08(1H,brs),8.28(1H,d,J=7.7Hz),8.34(1H,brs)
MS(ESI)
m/z 353[M+H]
+
Embodiment 28
3-((2-fluoro-5-trifluoromethyl) phenyl)-7-methyl-7,8-dihydro-6H-cinnolines-5-ketone synthetic
According to the method that is similar to reference example 1, use 2-bromo-2 '-fluoro-5 '-trifluoromethyl acetophenone replace 2-bromo-3 '-trifluoromethyl acetophenone, 5-methyl isophthalic acid, hydroresorcinol replaces 5-phenyl-1, hydroresorcinol, then handle the product that obtains like this, obtain target compound according to the method that is similar to reference example 2 and embodiment 1.
MS(ESI)
m/z 325[M+H]
+
Embodiment 29
3-((2-fluoro-5-trifluoromethyl) phenyl)-7-methyl-5,6,7,8-tetrahydrochysene cinnolines-5-alcohol synthetic
According to the method that is similar to embodiment 3, by handle 3-((2-fluoro-5-trifluoromethyl) the phenyl)-7-methyl-7 that obtains in embodiment 28,8-dihydro-6H-cinnolines-5-ketone obtains target compound.
MS(ESI)
m/z 327[M+H]
+
Embodiment 30
5,7-dimethyl-3-(3-trifluoromethyl)-5,6,7,8-tetrahydrochysene-cinnolines-5-alcohol synthetic
With the 5-oxo-3-(3-trifluoromethyl)-7 that obtains among the embodiment 66, (200 milligrams of 8-dihydros-6H-cinnolines, 0.65mmol) be dissolved in the tetrahydrofuran (THF) (1 milliliter), and be cooled to-20 ℃, (0.26 milliliter of the tetrahydrofuran solution that then in reaction liquid, adds the 3N methylmagnesium-chloride, 0.78mmol), reacted 3 hours, simultaneously elevated temperature.In reaction liquid, add distilled water (1 milliliter) and make the reaction quencher, then add ethyl acetate (5 milliliters) and the 1N sodium pyrosulfate aqueous solution (5 milliliters) extracts, with saturated brine solution (3 milliliters) washing organic layer, use anhydrous sodium sulfate drying, and use silica gel column chromatography (hexane/ethyl acetate=2/1 is to 1/1) purifying by concentrating the resistates that obtains, obtain the light yellow crystallization of target compound (74.1 milligrams, 35%).
MS(ESI)
m/z 323[M+H]
+
Embodiment 31
5-(N-(tertbutyloxycarbonyl)-L-alanyl) oxygen base-7-methyl-3-(3-trifluoromethyl)-5,6,7,8-tetrahydrochysene cinnolines synthetic
7-methyl-the 3-that will in embodiment 6, obtain (3-trifluoromethyl)-5,6,7,8-tetrahydrochysene cinnolines-5-alcohol (10 milligrams 0.03mmol) are dissolved in (0.5 milliliter of tetrahydrofuran (THF) and methylene dichloride, 0.5 in mixed solvent milliliter), then add N-ethyl-N '-(3-dimethylaminopropyl) carbodiimide (9 milligrams, 0.045mmol), N, (9 milligrams of N-dimethyl aminopyridine (catalytic amount) and N-(tertbutyloxycarbonyl)-L-L-Ala, 0.045mmol), at room temperature stir and spend the night.After reaction finishes, reaction liquid is concentrated, and use silica gel column chromatography (hexane/ethyl acetate 1/1) resistates that purifying obtains like this, obtain target compound.
MS(ESI)
m/z 480[M+H]
+
Embodiment 32
5-(L-alanyl) oxygen base-7-methyl-3-(3-trifluoromethyl)-5,6,7,8-tetrahydrochysene-cinnolines dihydrochloride synthetic
The 5-that will in embodiment 31, obtain (N-(tertbutyloxycarbonyl)-L-alanyl) oxygen base-7-methyl-3-(3-trifluoromethyl)-5,6,7,8-tetrahydrochysene cinnolines is dissolved in the diox (0.5 milliliter), then at the ice-cooled 4N HCl solution/diox (0.5 milliliter) that adds down, reaction is spent the night.Reaction liquid is concentrated into dried, obtains the target compound white solid.
MS(ESI)
m/z 380[M+H]
+
Embodiment 33
5-(N-(tert.-butoxy-carbonyl)-β-(tertiary butyl)-α-aspartyl) oxygen base-7-methyl-3-(3-trifluoromethyl)-5,6,7,8-tetrahydrochysene cinnolines synthetic
According to the method that is similar to embodiment 31, use N-(tertbutyloxycarbonyl)-β-(tertiary butyl)-α-aspartic acid to replace N-(tertbutyloxycarbonyl)-L-L-Ala, obtain target compound.
MS(ESI)
m/z 580[M+H]
+
Embodiment 34
5-(α-aspartyl) oxygen base-7-methyl-3-(3-trifluoromethyl)-5,6,7,8-tetrahydrochysene-cinnolines dihydrochloride synthetic
According to the method that is similar to embodiment 32; by handling 5-(N-(tertbutyloxycarbonyl)-β-(tertiary butyl)-α-aspartyl) the oxygen base-7-methyl-3-(3-trifluoromethyl)-5,6,7 that in embodiment 33, obtains; 8-tetrahydrochysene cinnolines obtains the target compound white solid.
MS(ESI)
m/z 424[M+H]
+
Embodiment 35
5-(N-(tertbutyloxycarbonyl)-α-(tertiary butyl)-β-aspartyl) oxygen base-7-methyl-3-(3-trifluoromethyl)-5,6,7,8-tetrahydrochysene cinnolines synthetic
According to the method that is similar to embodiment 31, use N-(tertbutyloxycarbonyl)-α-(tertiary butyl)-β-aspartic acid to replace N-(tertbutyloxycarbonyl)-L-L-Ala, obtain target compound.
MS(ESI)
m/z 580[M+H]
+
Embodiment 36
5-(β-aspartyl) oxygen base-7-methyl-3-(3-trifluoromethyl)-5,6,7,8-tetrahydrochysene-cinnolines dihydrochloride synthetic
According to the method that is similar to embodiment 32; by handling 5-(N-(tertbutyloxycarbonyl)-β-(tertiary butyl)-β-aspartyl) the oxygen base-7-methyl-3-(3-trifluoromethyl)-5,6,7 that in embodiment 35, obtains; 8-tetrahydrochysene cinnolines obtains the target compound white solid.
MS(ESI)
m/z 424[M+H]
+
Embodiment 37
5-(N-(tertbutyloxycarbonyl)-γ-(tertiary butyl)-α-Gu Anxianji) oxygen base-7-methyl-3-(3-trifluoromethyl)-5,6,7,8-tetrahydrochysene cinnolines synthetic
According to the method that is similar to embodiment 31, use N-(tertbutyloxycarbonyl)-γ-(tertiary butyl)-α-L-glutamic acid to replace N-(tertbutyloxycarbonyl)-L-L-Ala, obtain target compound.
MS(ESI)
m/z 594[M+H]
+
Embodiment 38
5-(α-Gu Anxianji) oxygen base-7-methyl-3-(3-trifluoromethyl)-5,6,7,8-tetrahydrochysene cinnolines dihydrochloride synthetic
According to the method that is similar to embodiment 32; by 5-(N-(tertbutyloxycarbonyl)-γ-(tertiary butyl)-α-Gu Anxianji) the oxygen base-7-methyl-3-(3-trifluoromethyl)-5,6,7 that obtains in the Processing Example 37; 8-tetrahydrochysene cinnolines obtains the target compound white solid.
MS(ESI)
m/z 438[M+H]
+
Embodiment 39
5-(N-(tertbutyloxycarbonyl)-α-(tertiary butyl)-γ-Gu Anxianji) oxygen base-7-methyl-3-(3-trifluoromethyl)-5,6,7,8-tetrahydrochysene cinnolines synthetic
According to the method that is similar to embodiment 31, use N-(tertbutyloxycarbonyl)-α-(tertiary butyl)-gamma-glutamic acid to replace N-(tertbutyloxycarbonyl)-L-L-Ala, obtain target compound.
MS(ESI)
m/z 594[M+H]
+
Embodiment 40
5-(Y-glutamyl) oxygen base-7-methyl-3-(3-trifluoromethyl)-5,6,7,8-tetrahydrochysene cinnolines dihydrochloride synthetic
According to the method that is similar to embodiment 32; by handling 5-(N-(tertbutyloxycarbonyl)-α-(tertiary butyl)-γ-Gu Anxianji) the oxygen base-7-methyl-3-(3-trifluoromethyl)-5,6,7 that in embodiment 39, obtains; 8-tetrahydrochysene cinnolines obtains target compound.
MS(ESI)
m/z 438[M+H]
+
Embodiment 41
5-(N-(tertbutyloxycarbonyl)-glycyl) oxygen base-7-methyl-3-(3-trifluoromethyl)-5,6,7,8-tetrahydrochysene cinnolines synthetic
According to the method that is similar to embodiment 31, use N-(tertbutyloxycarbonyl) glycine to replace N-(tertbutyloxycarbonyl)-L-L-Ala, obtain target compound.
MS(ESI)
m/z 466[M+H]
+
Embodiment 42
5-glycyl oxygen base-7-methyl-3-(3-trifluoromethyl)-5,6,7,8-tetrahydrochysene cinnolines dihydrochloride synthetic
According to the method that is similar to embodiment 32, by handle 5-(N-(tertbutyloxycarbonyl) glycyl) the oxygen base-7-methyl-3-(3-trifluoromethyl)-5,6,7 that obtains in embodiment 41,8-tetrahydrochysene cinnolines obtains target compound.
MS(ESI)
m/z 366[M+H]
+
Embodiment 43
5-(N-(tertbutyloxycarbonyl)-L-leucyl) oxygen base-7-methyl-3-(3-trifluoromethyl)-5,6,7,8-tetrahydrochysene cinnolines synthetic
According to the method that is similar to embodiment 31, use N-(tertbutyloxycarbonyl)-L-leucine in place N-(tertbutyloxycarbonyl)-L-L-Ala, obtain target compound.
MS(ESI)
m/z 480[M+H]
+
Embodiment 44
5-(L-leucyl oxygen base)-7-methyl-3-(3-trifluoromethyl)-5,6,7,8-tetrahydrochysene cinnolines dihydrochloride synthetic
According to the method that is similar to embodiment 32, by handle 5-(N-(tertbutyloxycarbonyl)-L-leucyl) the oxygen base-7-methyl-3-(3-trifluoromethyl)-5,6,7 that obtains in embodiment 43,8-tetrahydrochysene cinnolines obtains the target compound white solid.
MS(ESI)
m/z 380[M+H]
+
Embodiment 45
5-(N (α), N (ε)-(two-tertbutyloxycarbonyl)-L-lysyl) oxygen base-7-methyl-3-(3-trifluoromethyl)-5,6,7,8-tetrahydrochysene cinnolines synthetic
According to the method that is similar to embodiment 31, use N (α), N (ε)-(two-tertbutyloxycarbonyl)-L-Methionin to replace N-(tertbutyloxycarbonyl)-L-L-Ala, obtain target compound.
MS(ESI)
m/z 637[M+H]
+
Embodiment 46
5-(L-lysyl oxygen base)-7-methyl-3-(3-trifluoromethyl)-5,6,7,8-tetrahydrochysene cinnolines trihydrochloride synthetic
According to the method that is similar to embodiment 32, by 5-(N (α), N (ε)-(two-tertbutyloxycarbonyl)-L-lysyl) the oxygen base-7-methyl-3-(3-trifluoromethyl)-5 that obtains in the Processing Example 45,6,7,8-tetrahydrochysene cinnolines obtains the target compound white solid.
MS(ESI)
m/z 437[M+H]
+
Embodiment 47
5-(N-(tertbutyloxycarbonyl)-L-methionyl) oxygen base-7-methyl-3-(3-trifluoromethyl-phenyl)-5,6,7,8-tetrahydrochysene cinnolines synthetic
According to the method that is similar to embodiment 31, use N-(tertbutyloxycarbonyl)-L-methionine(Met) to replace N-(tertbutyloxycarbonyl)-L-L-Ala, obtain target compound.
MS(ESI)
m/z 539[M+H]
+
Embodiment 48
5-(L-methionyl) oxygen base-7-methyl-3-(3-trifluoromethyl)-5,6,7,8-tetrahydrochysene cinnolines dihydrochloride synthetic
According to the method that is similar to embodiment 32, by handle 5-(N-(tertbutyloxycarbonyl)-L-methionyl) the oxygen base-7-methyl-3-(3-trifluoromethyl)-5,6,7 that obtains in embodiment 47,8-tetrahydrochysene cinnolines obtains the target compound white solid.
MS(ESI)
m/z 439[M+N]
+
Embodiment 49
5-(N-(tertbutyloxycarbonyl)-L-phenylalanyl) oxygen base-7-methyl-3-(3-trifluoromethyl-phenyl)-5,6,7,8-tetrahydrochysene cinnolines synthetic
According to the method that is similar to embodiment 31, use N-(tertbutyloxycarbonyl)-L-phenylalanine to replace N-(tertbutyloxycarbonyl)-L-L-Ala, obtain target compound.
MS(ESI)
m/z 556[M+H]
+
Embodiment 50
5-(L-phenylalanyl) oxygen base-7-methyl-3-(3-trifluoromethyl)-5,6,7,8-tetrahydrochysene cinnolines dihydrochloride synthetic
According to the method that is similar to embodiment 32, by handle 5-(N-(tertbutyloxycarbonyl)-L-phenylalanyl) the oxygen base-7-methyl-3-(3-trifluoromethyl)-5,6,7 that obtains in embodiment 49,8-tetrahydrochysene cinnolines obtains the target compound white solid.
MS(ESI)
m/z 456[M+H]
+
Embodiment 51
5-(L-prolyl) oxygen base-7-methyl-3-(3-trifluoromethyl)-5,6,7,8-tetrahydrochysene cinnolines dihydrochloride synthetic
According to the method that is similar to embodiment 32, by handle in embodiment 8, obtain, as cis-5-(N-(tertbutyloxycarbonyl)-L-prolyl) oxygen base-7-methyl-3-(3-trifluoromethyl)-5,6,7 of high polar compound, 8-tetrahydrochysene cinnolines obtains the target compound white solid.
MS(ESI)
m/z 406[M+H]
+
Embodiment 52
5-(N-(tertbutyloxycarbonyl)-L-valyl) oxygen base-7-methyl-3-(3-trifluoromethyl)-5,6,7,8-tetrahydrochysene cinnolines synthetic
According to the method that is similar to embodiment 31, use N-(tertbutyloxycarbonyl)-L-Xie Ansuan to replace N-(tertbutyloxycarbonyl)-L-L-Ala, obtain target compound.
MS(ESI)
m/z 508[M+H]
+
Embodiment 53
5-(L-valyl oxygen base)-7-methyl-3-(3-trifluoromethyl)-5,6,7,8-tetrahydrochysene cinnolines dihydrochloride synthetic
According to the method that is similar to embodiment 32, by handle 5-(N-(tertbutyloxycarbonyl)-L-valyl) the oxygen base-7-methyl-3-(3-trifluoromethyl)-5,6,7 that obtains in embodiment 52,8-tetrahydrochysene cinnolines obtains the target compound white solid.
1H-NMR (200MHzFT, TMS, DMSO-d
6) 1.02 (3H, d, J=6.9Hz), 1.07 (3H, d, J=6.9Hz), 1.17 (3H, d, J=6.4Hz), 1.54 (1H, q, J=11.6Hz), 2.10-2.45 (3H, complicated peak), 2.81 (1H, dd, J=11.1,17.5Hz), 2.37-2.59 (2H, complicated peak), (2.78-3.14 2H, complicated peak), and 3.51-3.67 (1H, m), 3.92 (3H, s), 6.11 (1H, dd, J=6.1,10.1Hz), 7.82 (1H, t, J=7.7Hz), 7.92 (1H, d, J=7.9Hz), 8.55 (1H, s), 8.63 (1H, d, J=7.7Hz), 8.68 (1H, s), 8.85-9.03 (2H, br) [α]
D 25+ 105.2 ° (cl.016, MeOH)
m.p.201-3℃
MS(ESI)
m/z 408[M+H]
+
Embodiment 54
(5S, 7S)-5-(N-(tert.-butoxy-carbonyl)-D-phenylalanyl) oxygen base-7-methyl-3-(3-trifluoromethyl)-5,6,7,8-tetrahydrochysene cinnolines synthetic
To the 7-methyl-3-that in embodiment 6, obtains (3-trifluoromethyl)-5,6,7,8-tetrahydrochysene cinnolines-5-alcohol (27.8 grams, 90.4mmol) N, add 1-[3-(dimethylamino) propyl group in the dinethylformamide solution (181 milliliters)]-3-ethyl-carbodiimide hydrochloride (26 grams, 135.7mmol) and N-(tertbutyloxycarbonyl)-D-phenylalanine (31.2 grams, 117.6mmol), wash with N-Methyl pyrrolidone (36 milliliters), then ice-cooled following, in mixing liquid, add N, (1.2 milligrams of N-dimethyl aminopyridines, 9.0mmol), stirring is spent the night, and adds ethyl acetate (0.6 milliliter) and distilled water (0.3L), and with the aqueous potassium hydrogen sulfate (400 milliliters) of 5% weight percent, the organic layer that saturated sodium bicarbonate aqueous solution (300 milliliters) and the washing of 10% salt brine solution (300 milliliters) order are extracted like this.Add ethanol (187mL) in the resistates that after organic layer concentrates, obtains, and at room temperature stir and spend the night.The crystallization that generates is filtered and washed with ethanol (35 milliliters), obtain title target compound (14.8 gram).
1H-NMR (200MHzFT, TMS, CDCl
3) 1.18 (3H, d, J=6.5Hz), 1.22-1.38 (1H, m), 71 (9H, s), 1.90-2.23 (2H, complicated peak), 2.72 (1H, dd, J=11.5,17.9Hz), 3.10 (2H, d, J=7.1Hz), 3.40 (1H, ddd, J=1.4,5.0,17.7Hz), 4.52 (1H, q, J=7.1Hz), 5.02 (1H, d, J=6.5Hz), 6.07 (1H, dd, J=5.9,11.1Hz), (7.01-7.40 5H, complicated peak), 7.60 (1H, t, J=7.8Hz), 7.92 (1H, s), 8.32 (1H, d, J=7.7Hz), 8.55 (1H, s)
MS(ESI)
m/z 556[M+H]
+
Embodiment 55
(5S, 7S)-7-methyl-3-(3-trifluoromethyl)-5,6,7,8-tetrahydrochysene cinnolines-5-alcohol synthetic
At room temperature; to (the 5S that in embodiment 54, obtains; 7S)-5-(N-(tertbutyloxycarbonyl)-D-phenylalanyl) oxygen base-7-methyl-3-(3-trifluoromethyl)-5; 6; 7; add the 1N NaOH aqueous solution (0.6L) in the methanol solution (1.2L) of 8-tetrahydrochysene cinnolines (280 grams, 0.5 mole), then react down and spend the night at 40 ℃.Reaction liquid is cooled to 10 ℃, then adds distilled water (1.8L), stirred 4 hours under floating condition, filtering for crystallizing obtains title compound.The compound that obtains like this with in embodiment 10, obtain identical.
Embodiment 56
(5R, 7R)-5-(N-(tert.-butoxy-carbonyl)-L-valyl) oxygen base-7-methyl-3-(3-trifluoromethyl-phenyl)-5,6,7,8-tetrahydrochysene cinnolines synthetic
According to the method that is similar to embodiment 54, use N-(tertbutyloxycarbonyl)-L-Xie Ansuan to replace N-(tertbutyloxycarbonyl)-L-phenylalanine, obtain target compound.
1H-NMR (200MHzFT, TMS, CDCl
3) 1.03 (6H, dd, J=5.7,6.8Hz), 1.24 (3H, d, J=6.6Hz), 1.48 (9H, s), 1.51-1.69 (1H, m), 2.04-2.37 (3H, complicated peak), 2.79 (1H, dd, J=11.4,17.9Hz), 3.44 (1H, ddd, J=1.7,4.9,17.9Hz), 4.15 (1H, dd, J=6.0,7.9Hz), 5.01 (1H, d, J=7.8Hz), 6.18 (1H, dd, J=4.7Hz), 7.61 (1H, t, J=7.8Hz), 7.73 (1H, d), 8.00 (1H, s), 8.35 (1H, d, J=7.4Hz), 8.56 (1H, s) MS (ESI)
m/z 508[M+H]
+
Embodiment 57
(5R, 7R)-7-methyl-3-(3-trifluoromethyl)-5,6,7,8-tetrahydrochysene cinnolines-5-alcohol synthetic
According to the method that is similar to embodiment 55, by obtain in the Processing Example 56 (5R, 7R)-5-(N-(tertbutyloxycarbonyl)-L-valyl) oxygen base-7-methyl-3-(3-trifluoromethyl)-5,6,7,8-tetrahydrochysene cinnolines obtains the title target compound.The compound that obtains like this with in embodiment 9, obtain identical.
Embodiment 58
(-)-(5R, 7R)-5-(L-valyl) oxygen base-7-methyl-3-(3-trifluoromethyl)-5,6,7,8-tetrahydrochysene cinnolines dihydrochloride synthetic
According to the method that is similar to embodiment 32, by handle in embodiment 56, obtain (5R, 7R)-5-(N-(tert.-butoxy-carbonyl)-L-valyl) oxygen base-7-methyl-3-(3-trifluoromethyl-phenyl)-5,6,7,8-tetrahydrochysene cinnolines obtains title target compound white solid.
1H-NMR (200MHzFT, TMS, DMSO-d
6) 0.87-1.22 (10H, complicated peak), 1.60 (1H, q, J=12.0Hz), 2.12-2.40 (3H, complicated peak), 2.81 (1H, dd, J=11.4,17.6Hz), 3.30 (1H, dd, J=4.3,17.6Hz), 4.04 (1H, t, J=4.8Hz), 6.22 (1H, dd, J=5.9,10.6Hz), 7.81 (1H, t, J-7.8Hz), 7.92 (1H, d, J=8.0Hz), 8.46-8.70 (2H, complicated peak), 8.82-9.04 (2H, br)
[α]
D 25-68.8°(cO.999,MeOH)
m.p.162-5℃
MS(FAB)
m/z 408[M+H]
+
Embodiment 59
(5S, 7R)-5-(N-(tert.-butoxy-carbonyl)-L-valyl) oxygen base-7-methyl-3-(3-trifluoromethyl-phenyl)-5,6,7,8-tetrahydrochysene cinnolines synthetic
Use N-(tertbutyloxycarbonyl)-L-Xie Ansuan replace among the embodiment 7 the 4-nitrobenzoic acid and with (5R, 7R)-7-methyl-3-(3-trifluoromethyl)-5,6,7,8-tetrahydrochysene cinnolines-5-alcohol replaces the 7-methyl-3-(3-trifluoromethyl)-5,6 among the embodiment 7,7,8-tetrahydrochysene cinnolines-5-alcohol by the Mitsunobu reaction, obtains title compound.
MS(ESI)
m/z 508[M+H]
+
Embodiment 60
(5S, 7R)-7-methyl-3-(3-trifluoromethyl)-5,6,7,8-tetrahydrochysene cinnolines-5-alcohol synthetic
According to the method that is similar to embodiment 55, by obtain in the Processing Example 59 (5S, 7R)-5-(N-(tertbutyloxycarbonyl)-L-valyl) oxygen base-7-methyl-3-(3-trifluoromethyl)-5,6,7,8-tetrahydrochysene cinnolines obtains the title target compound.
Embodiment 61
(+)-(5S, 7R)-5-(L-valyl) oxygen base-7-methyl-3-(3-trifluoromethyl)-5,6,7,8-tetrahydrochysene cinnolines dihydrochloride synthetic
According to the method that is similar to embodiment 32, by obtain in the Processing Example 59 (5S, 7R)-5-(N-(tertbutyloxycarbonyl)-L-valyl) oxygen base-7-methyl-3-(3-trifluoromethyl)-5,6,7,8-tetrahydrochysene cinnolines obtains the title target compound.
1H-NMR (200MHzFT, TMS, DMSO-d
6) 0.92 (3H, d, J=3.7Hz), 0.96 (3H, d, J=3.7Hz), 1.13 (3H, d, J=6.6Hz), 1.72-1.92 (1H, m), 2.02-2.36 (3H, complicated peak), 2.72 (1H, dd, J=11.4,17.6Hz), 3.36 (1H, dd, J=4.3,17.6Hz), 3.79 (1H, brt, J=4.5Hz), 6.12 (1H, brs), 7.82 (1H, t, J=7.6Hz), 7.92 (1H, d, J=8.0Hz), 7.98-8.50 (1H, br), 8.52 (1H, d, J-8.5Hz), 8.60 (1H, s), 8.70-8.88 (2H, br)
[α]
D 25+36.9°(c0.975,MeOH)
m.p.186-9℃
MS(FAB)
m/z 408[M+H]
+
(5R, 7S)-5-(N-(tert.-butoxy-carbonyl)-L-valyl) oxygen base-7-methyl-3-(3-trifluoromethyl-phenyl)-5,6,7,8-tetrahydrochysene cinnolines synthetic
Use N-(tertbutyloxycarbonyl)-L-Xie Ansuan replace among the embodiment 7 the 4-nitrobenzoic acid and with (5S, 7S)-7-methyl-3-(3-trifluoromethyl)-5,6,7,8-tetrahydrochysene cinnolines-5-alcohol replaces the 7-methyl-3-(3-trifluoromethyl)-5,6 among the embodiment 7,7,8-tetrahydrochysene-cinnolines-5-alcohol by the Mitsunobu reaction, obtains title compound.
MS(ESI)
m/z 508[M+H]
+
Embodiment 63
(5R, 7S)-7-methyl-3-(3-trifluoromethyl)-5,6,7,8-tetrahydrochysene cinnolines-5-alcohol synthetic
According to the method that is similar to embodiment 55, by obtain in the Processing Example 62 (5R, 7S)-5-(N-(tertbutyloxycarbonyl)-L-valyl) oxygen base-7-methyl-3-(3-trifluoromethyl)-5,6,7,8-tetrahydrochysene cinnolines obtains the title target compound.
Embodiment 64
(-)-(5R, 7S)-5-(L-valyl) oxygen base-7-methyl-3-(3-trifluoromethyl)-5,6,7,8-tetrahydrochysene cinnolines dihydrochloride synthetic
According to the method that is similar to embodiment 32, by obtain in the Processing Example 62 (5R, 7S)-5-(N-(tertbutyloxycarbonyl)-L-valyl) oxygen base-7-methyl-3-(3-trifluoromethyl)-5,6,7,8-tetrahydrochysene cinnolines obtains the title target compound.
1H-NMR (200MHzFT, TMS, DMSO-d
6) 0.95-1.06 (6H, complicated peak), 1.15 (3H, d, J=6.6Hz), (1.77-2.34 4H, complicated peak), 2.74 (1H, dd, J=10.9,17.4Hz), 3.37 (1H, dd, J=4.2,17.5Hz), 3.75-3.90 (1H, m), 6.20 (1H, brt, J=3.3Hz), 7.82 (1H, t, J=7.7Hz), 7.93 (1H, t, J=7.7Hz), 8.50-8.59 (2H, complicated peak), 8.70-8.88 (3H, complicated peak)
[α]
D 25-15.8°(cl.010,MeOH)
m.p.181-5℃
MS(FAB)
m/z 408[M+H]
+
Reference example 1
3-hydroxyl-2-[2-oxo-2-(3-trifluoromethyl) ethyl]-5-phenyl hexamethylene-2-ketenes synthetic
To 2-bromo-3 '-trifluoromethyl acetophenone (534.1 milligrams, 2mmol) and 5-phenyl-hydroresorcinol (376.5 milligrams add salt of wormwood (276.4 milligrams 2mmol), are stirred and spend the night in chloroformic solution 2mmol) (2 milliliters) under room temperature and floating condition.In reaction liquid, add ethyl acetate (5 milliliters), leach insolubles, then under reduced pressure concentrate the organic layer that obtains like this, and the spissated resistates of use silica gel column chromatography (hexane/ethyl acetate=1/1) purifying, obtain thick product, it is further purified by suspended pattern (about 0.2 milliliter of 1 milliliter/ethyl acetate of hexane), obtains target compound (257.8 milligrams, 35.0%).
MS(ESI)
m/z 375[M+H]
+
Reference example 2
7-phenyl-3-(3-trifluoromethyl)-4,6,7,8-tetrahydrochysene-1H-cinnolines-5-ketone synthetic
To 3-hydroxyl-2-[2-oxo-2-(3-the trifluoromethyl)-ethyl that in reference example 1, obtains]-(257.8 milligrams of 5-phenyl-hexamethylenes-2-ketenes, 0.69mmol) ethanolic soln (1 milliliter) in add (72.3 milligrams of hydrazine hydrochlorides, 0.69mmol) and (0.19 milliliter of triethylamine, 1.38mmol), and at room temperature stirred 1 hour.In reaction liquid, add distilled water (3 milliliters), filter out the yellow crystal of generation, obtain the thick product of target (603 milligrams).
MS(ESI)
m/z 375[M+H]
+
Reference example 3
Synthesizing of 3-hydroxyl-5-oxo-hexamethylene-3-olefinic carboxylic acid ethyl ester
To 3, (25 restrain the 5-protocatechuic acid, add sulfuric acid (3 milliliters) in ethanolic soln 162.2mmol) (200 milliliters), and at room temperature stir and spend the night, and heat 4 days down at 65 ℃ then.The concentrating under reduced pressure reaction liquid, and pour in the frozen water (about 300mL), stir simultaneously, leach white crystal, 3,5-protocatechuic acid ethyl ester (22.8g, 77.2%).
With 3,5-protocatechuic acid ethyl ester (10 grams, 54.89mmol) be dissolved in the ethanol (15 milliliters), then add sodium formiate (4.48 grams, 65.87mmol), filled nitrogen 15 minutes 30 ℃ of downhill reaction device inside, add palladium/carbon (364 milligrams), reacted 3 hours down at 30 ℃, react down at 40 ℃ then and spend the night.Leach catalyzer, then with the neutralization of 1N HCl solution, concentrating under reduced pressure, and, obtain target compound (1.53g, 15.1%) with the resistates that silica gel column chromatography (hexane/ethyl acetate=1/1 is to 0/1) purifying obtains like this.
1H-NMR(200MHzFT,TMS,CDCl
3)
1.26(3H,dt,J=1.8,7.1Hz),2.66(2H,d,J=2.7Hz),2.83(1H,dd,J=1.8,6.6Hz),3.01-3.19(1H,m),3.32-3.55(1H,m),4.18(2H,q,J=7.2Hz),5.51(1H,s),5.80-6.10(1H,br)MS(ESI)
m/z 185[M+H]
+
Reference example 4
5-hydroxyl-1-methyl isophthalic acid, 6-dihydro-2H-pyridine-3-ketone synthetic
To the sarcosine carbethoxy hydrochloride (3.06 grams, add in ethanolic soln 20mmol) (30 milliliters) sodium bicarbonate (3.36 grams, 40mmol) and martonite (1.68 milliliters, 20mmol), and 60 ℃ down stirring spend the night.Filtering reaction liquid, concentrating under reduced pressure then adds 10%HCl solution (250 milliliters) in the resistates that obtains like this and ethyl acetate (250 milliliters) is carried out fractionation.In the water layer that obtains like this, add sodium bicarbonate,, then use ethyl acetate extraction, use anhydrous magnesium sulfate drying up to pH>7, and concentrating under reduced pressure, target compound obtained, N-methyl-N-(2-oxopropyl)-glycine ethyl ester (2.58 grams, 74%).The compound that obtains like this is dissolved in the trimethyl carbinol (40 milliliters), and (1.67 grams 14.9mmol) also at room temperature stirred 30 minutes then to add potassium tert.-butoxide.The concentrating under reduced pressure reaction liquid, and the resistates that will obtain like this (purifying of chloroform/methanol/30% ammoniacal liquor=6/2.5/0.5) obtains target compound (1.83g, 96%) with silica gel column chromatography.
MS(ESI)
m/z 128[M+H]
+
Reference example 5
1-benzyl-5-hydroxyl-1,6-dihydro-2H-pyridine-3-ketone synthetic
According to the method that is similar to reference example 4, use sarcosine ethyl ester hydrochloride to replace N-benzyl glycine ethyl ester hydrochloride, obtain target compound.
MS(ESI)
m/z 204[M+H]
+
Embodiment 65
7-methyl-3-(3-three fluoro-aminomethyl phenyls)-4,6,7,8-tetrahydrochysene-1H-cinnolines-5-ketone synthetic
To 3-hydroxy-5-methyl base-2-[2-oxo-2-(3-the trifluoromethyl)-ethyl that in reference example 7, obtains]-(438.7 milligrams of hexamethylenes-2-ketenes, 1.4mmol) ethanolic soln (14 milliliters) in add (177 milligrams of hydrazine hydrochlorides, 1.7mmol) and (0.49 milliliter of triethylamine, 35mmol), at room temperature stir 3 hours.Reaction liquid is concentrated, then use silica gel column chromatography (methylene chloride=30/1) purifying resistates, obtain target compound (100.9mg, 23.3%).
1H-NMR (200MHzFT, TMS, CDCl
3) 1.13 (3H, d, J=5.9Hz), 2.00-2.60 (5H, complicated peak), 3.27 (1H, d, J=9.3Hz), 3.57 (1H, d, J=9.3Hz), 7.49 (1H, brs), 7.54 (1H, brd, J=7.9Hz), 7.65 (1H, brd, J=7.7Hz), 7.94 (1H, brd, J=7.8Hz), 8.08 (1H, brs)
MS(ESI)
m/z 309[M+H]
+
Embodiment 66
7-methyl-3-(3-three fluoro-aminomethyl phenyls)-7,8-dihydro-6H-cinnolines-5-ketone synthetic
To the 7-methyl-3-that in embodiment 65, obtains (3-trifluoromethyl)-4,6,7, (136.2 milligrams of 8-tetrahydrochysenes-1H-cinnolines-5-ketone, 0.44mmol) pyridine solution (1 milliliter) in add tosic acid hydrate (84 milligrams 0.44mmol), and were at room temperature stirred 3 days.Reaction liquid is concentrated, then use silica gel column chromatography (methylene chloride=30/1) purifying resistates, obtain target compound (89.0mg, 66.1%).
1H-NMR (200MHzFT, TMS, CDCl
3) 1.28 (3H, d, J=1.3Hz), 2.40-2.62 (2H, complicated peak), and 2.80-2.89 (1H, m), 2.90-3.19 (1H, m), and 3.55-3.70 (1H, m), 7.68 (1H, brt, J=7.7Hz), 7.74 (1H, brd, J=7.7H z), 8.29 (1H, s), 8.34 (1H, brd, J=7.3Hz), 8.44 (1H, brs)
MS(ESI)
m/z 307[M+H]
+
Embodiment 67
Synthesizing of [7-methyl-3-(3-trifluoromethyl)-7,8-dihydro-6H-cinnolines-5-subunit]-hydrazine
To the 7-methyl-3-that in embodiment 65, obtains (3-trifluoromethyl)-4,6,7, (230 milligrams of 8-tetrahydrochysenes-1H-cinnolines-5-ketone, 0.74mmol) ethanolic soln (3 milliliters) in add (77.3 milligrams of hydrazine hydrochlorides, 0.74mmol) and triethylamine (0.206 milliliter 1.48mmol), is at room temperature stirred and spends the night.Reaction liquid is concentrated, then use silica gel column chromatography (hexane/ethyl acetate=1/1) purifying resistates, obtain target compound (29.5mg, 12.5%).
1H-NMR (200MHzFT, TMS, CDCl
3) 1.26 (3H, d, J=1.3Hz), 2.03 (1H, dd, J=10.6,16.4Hz), 2.06-2.36 (1H, m), 2.75 (1H, ddd, J=1.6,4.4,16.4Hz), 2.83 (1H, dd, J=10.8,16.5Hz), 3.49 (1H, ddd, J=1.5,3.6,16.5Hz), 4.5-6.5 (2H, m), 7.65 (1H, t, J=7.7Hz), 7.75 (1H, d, J=7.8Hz), 8.26-8.47 (3H, complicated peak)
MS(ESI)
m/z 321[M+H]
+
Embodiment 68
3-(3-trifluoromethyl)-7,8-dihydro-6H-cinnolines-5-ketone synthetic
By using 1, hydroresorcinol replaces the 5-methyl isophthalic acid of use in the reference example 7, hydroresorcinol reacts, and then according to the method that is similar to embodiment 65, handle the product obtain like this according to the method that is similar to embodiment 66 then, obtains target compound.
MS(ESI)
m/z 293[M+H]
+
Embodiment 69
7,7-dimethyl-3-(3-trifluoromethyl)-7,8-dihydro-6H-cinnolines-5-ketone synthetic
By using 5,5-dimethyl-hydroresorcinol replaces the 5-methyl isophthalic acid of use in the reference example 7, and hydroresorcinol reacts, then according to the method that is similar to embodiment 65, handle the product obtain like this according to the method that is similar to embodiment 66 then, obtain target compound.
MS(ESI)
m/z 321[M+H]
+
Reference example 6
2-bromo-3 '-trifluoromethyl acetophenone synthetic
Under ice-cooled, to can commercial buy 3 '-trifluoromethyl acetophenone (79.6 grams, 0.423 add pyridine bromide perbromide (0.423 mole of 135.4 gram) in the toluene solution (423 milliliters) mole), and stirred 5 hours, be heated to room temperature simultaneously, reaction liquid with ice cooling once more, is then dripped 400 ml distilled waters, reaction is stopped and fractionation.With 400mL saturated sodium bicarbonate aqueous solution washing toluene layer, then use anhydrous magnesium sulfate drying, and concentrating under reduced pressure and underpressure distillation, obtain target compound (92.35g, 81.7%).
1H-NMR(200MHzFT,TMS,CDCl
3)4.46(2H,s),7.66(1H,brt,J=7.9Hz),7.88(1H,brd,J=7.6Hz),8.19(1H,brd,J=7.5Hz),8.25(1H,brs)
B.p.92 ℃/3 mmhg
Reference example 7
3-hydroxy-5-methyl base-2-[2-oxo-2-(3-trifluoromethyl)-ethyl]-hexamethylene-2-ketenes synthetic
To the 5-methyl isophthalic acid, hydroresorcinol (30 gram, 0.238 mole) and the 2-bromo-3 that in reference example 6, obtains '-add salt of wormwood (32.9 grams in the chloroformic solution (240 milliliters) of trifluoromethyl acetophenone (63.5 grams, 0.238 mole), 0.238 mole), at room temperature stirring is spent the night.Reaction liquid is filtered, obtain white solid, it is suspended in the distilled water (300mL), then at the ice-cooled dense HCl solution (300mL) that drips down, extract with ethyl acetate (700mL) and ethanol (50mL), use anhydrous sodium sulfate drying, the organic layer that concentrating under reduced pressure obtains like this adds ethyl acetate (200mL) in the resistates that obtains, at room temperature stirred suspension is 4 hours, leach crystallization, obtain target compound (25.7mg, 34.6%).
1H-NMR (200MHzFT, TMS, CDCl
3) 1.06 (3H, d, J=5.9Hz), 1.98-2.63 (5H, complicated peak), 3.77 (1H, d, J=13.6Hz), 4.29 (1H, d, J=13.6Hz), 7.63 (1H, brt, J=7.6Hz), 7.87 (1H, brd, J=7.8Hz), 8.43-8.52 (2H, complicated peak), 9.64 (1H, s) MS (ESI)
m/z 313[M+H]
+
Embodiment 70
Synthesizing of 7-methyl-3-(3-trifluoromethyl) cinnolines-5-alcohol
To the 7-methyl-3-that in embodiment 66, obtains (3-trifluoromethyl)-7, (306 milligrams of 8-dihydros-6H-cinnolines-5-ketone, 1.0mmol) ethyl acetate solution (1 milliliter) in add (446 milligrams of cupric bromides, 2.0mmol), then reacted 8 hours in heating and under refluxing, in reaction liquid, add saturated sodium bicarbonate aqueous solution (2 milliliters), and use ethyl acetate extraction.Add ethyl acetate (1mL) in the resistates that after the concentrating under reduced pressure organic layer, obtains, leach the solid that obtains, obtain target product (17mg, 5.5%) yellow solid.
1H-NMR (200MHzFT, TMS, DMSO-d
6) 2.54 (3H, s), 7.02 (1H, s), 7.79 (1H, s), 7.80-7.95 (2H, complicated peak), 8.52-8.69 (2H, complicated peak), 11.1 (1H, s)
MS(ESI)
m/z 305[M+H]
+
Embodiment 71
Synthesizing of 5-methoxyl group-7-methyl-3-(3-trifluoromethyl) cinnolines
To (30.4 milligrams of the 7-methyl-3-that in embodiment 70, obtains (3-trifluoromethyl) cinnolines-5-alcohol, 0.1mmol) acetone soln (5 milliliters) in add (0.006 milliliter of methyl iodide, 0.11mmol) and salt of wormwood (13.8 milligrams 0.11mmol), are then at room temperature reacted and spend the night.In the resulting resistates of concentrating under reduced pressure reaction liquid, add distilled water (1mL), and use ethyl acetate extraction.Resistates with obtaining after silica gel column chromatography (hexane/ethyl acetate=1/1) the purifying concentrating under reduced pressure organic layer obtains target compound (5mg, 15%) white solid.
MS(ESI)
m/z 319[M+H]
+
Embodiment 72
Synthesizing of 5-acetoxyl group-7-methyl-3-(3-trifluoromethyl) cinnolines
(60 milligrams, adding diacetyl oxide (3mL) in pyridine solution 0.2mmol) (2 milliliters) then at room temperature reacts and spends the night to the 7-methyl-3-that obtains in embodiment 70 (3-trifluoromethyl) cinnolines-5-alcohol.The concentrating under reduced pressure reaction liquid, then add distilled water (1mL), use ethyl acetate extraction, and with resulting resistates after HPLC column chromatography (hexane/ethyl acetate=3/1) the purifying concentrating under reduced pressure organic layer, obtain target compound (25mg, 36%) light yellow solid.
MS(ESI)
m/z 347[M+H]
+
Embodiment 73
Synthesizing of 5-benzyloxy 7-methyl-3-(3-trifluoromethyl) cinnolines
To (69 milligrams of the 7-methyl-3-that in embodiment 70, obtains (3-trifluoromethyl) cinnolines-5-alcohol, 0.2mmol) acetone soln (5 milliliters) in add (28 milligrams in bromotoluene (0.024 milliliter) and salt of wormwood, 0.2mmol), then at room temperature stir and spend the night, and under heating, refluxed 3 hours.Further in reaction liquid, add bromotoluene (0.024mL) and salt of wormwood (28mg, 0.2mmol), then at room temperature stir and spend the night, the concentrating under reduced pressure reaction liquid, add distilled water (1mL), use ethyl acetate extraction, and with HPLC column chromatography (hexane/ethyl acetate=3/1) purifying concentrating under reduced pressure organic layer resulting resistates afterwards, obtain target compound (8mg, 10%).
MS(ESI)
m/z 395[M+H]
+
Experimental example 1
Use the extracorporeal anti-tumor effect of breast tumor cell MCF-7 and MDA-MB-453
Use has added 10% serum RPMI, 1640 substratum (Asahi Technoclass Inc's), and 2000 MCF-7 cells and 4000 MDA-MB-453 cells are inoculated in the 96 hole flat boards separately.After these cells of cultivation under 37 ℃, under the atmosphere of 5% carbonic acid gas/95% air 24 hours, add embodiment 1,2,6,9-13,20,24,26,27,65,66,70,71, each compound of 72 and 73, and further cultivated 3 days.Cell is dyeed with 0.05% methylene blue solution, and use microtest plate reader (Benchmark Plus, Bio-Rad Laboratories) to be determined at the absorbancy of 660 nanometers.Calculate proliferation inhibition rate by following formula, embodiment 1,2,6,9-13, and 20,24,26,27,65,66,70,71,50% cell inhibitory effect concentration of 72 and 73 compound sees Table 2.
Proliferation inhibition rate=(1-adds the absorbancy of the absorbancy/contrast of medicine) * 100
Table 2
IC 50(μg/ml) | ||
MCF-7 | MDA-MB-453 | |
The compound of embodiment 1 | 0.0388 | 0.0395 |
The compound of embodiment 2 | 1.9600 | 1.5700 |
The compound of embodiment 6 | 0.0499 | 1.4700 |
The compound of embodiment 9 | 0.0772 | 0.3390 |
The compound of embodiment 10 | 0.0982 | 1.5400 |
The compound of embodiment 11 | 0.0455 | 0.8480 |
The compound of embodiment 13 | 0.0671 | 0.9510 |
The compound of embodiment 20 | 1.4060 | 9.3500 |
The compound of embodiment 24 | 3.5700 | 4.9500 |
The compound of embodiment 26 | 0.3610 | 8.9300 |
The compound of embodiment 27 | 0.2710 | 4.7200 |
The compound of embodiment 65 | 0.10 | 1.64 |
The compound of embodiment 66 | 0.05 | 1.26 |
The compound of embodiment 70 | 0.181 | 0.551 |
The compound of embodiment 71 | 0.158 | 3.360 |
The compound of embodiment 72 | 0.138 | 0.420 |
The compound of embodiment 73 | 0.399 | 2.600 |
Find out significantly that from table 2 embodiment 1,2,6,9-13,20,24,26,27,65,66,70,71,72 and 73 compound has the antitumous effect that suppresses breast tumor cell propagation.
Further, under condition same as above, use 4000 breast tumor cell T-47D, the compound that adds embodiment 65 or 66 is tested.IC
50Value is respectively 0.67 mcg/ml and 0.28 mcg/ml, and compound also demonstrates the antitumous effect at breast tumor cell T-47D.
Experimental example 2
Use the anti-tumor in vivo effect of breast tumor cell ZR-75-1
Breast tumor cell ZR-75-1 is seeded in the back subcutaneous area of female nude mice.The point that begins logarithmic growth from tumour cell begins, and with the dosage level orally give embodiment 66 of 500mg/kg and the compound of embodiment 53, once a day, gives 14 days continuously.In time dependent mode, measure the conjugate axis and the transverse axis of tumour, and calculate gross tumor volume by following formula.Calculate relative tumour volume, the gross tumor volume when wherein will begin administration is defined as 1.Effect is judged divided by the value of the gross tumor volume (T/C) of control group by the gross tumor volume of treatment group.
Gross tumor volume=conjugate axis * conjugate axis * transverse axis/2
The 15th day the T/C value that begins to give after the compound of embodiment 66 and embodiment 53 is respectively 30.3% and 34.0%.Therefore, the compound of embodiment 66 and embodiment 53 shows to have the antitumous effect that suppresses the mammary tumor proliferation in vivo equally.
Industrial applicibility
According to the present invention, acceptable salt on the cinnolines analog that can effectively be used for prevention or treatment tumour or its physiology is provided, and has comprised that acceptable salt is as antitumor agent and the cell proliferation inhibitor of active component on cinnolines analog or its physiology.
Claims (14)
1. comprise 3-phenyl-cinnolines analogue by following general formula (1) or (2) representative, or on its physiology acceptable salt as the antineoplastic agent of active ingredient:
Wherein J is A-C-B (C is a carbon atom); A is that (O is a Sauerstoffatom to the O-Y group; Y is a hydrogen atom, the low alkyl group that can be replaced by phenyl, lower acyl or can protected amino-acid residue); B is a hydrogen atom, low alkyl group, or form the imino-of carbonyl or replacement with A; K is (CH
2)
qL is N-W (N is a nitrogen-atoms) or W-C-W ' (C is a carbon atom); Each is to have the low alkyl group that is selected from hydroxyl, lower alkoxy and phenyl substituent independently for W and W ', phenyl, carboxyl, lower alkoxycarbonyl or hydrogen atom; M is (CH
2)
m, or J-K-L-M is C (O-Y)=CH-C (W)-CH (Y has and above identical implication with W), Z is Sauerstoffatom or N-Q (Q is amino, low-grade alkyl amino, hydroxyl or lower alkoxy); Each is low alkyl group independently for X and X ', lower alkoxycarbonyl, rudimentary amido, lower alkoxy, halogenated lower alkyl, nitro, cyano group, halogen atom or hydrogen atom; Each is 0 to 3 integer independently for m and q; And each is 0 or 1 independently for n and n '.
2. according to the antineoplastic agent of claim 1, wherein 3-phenyl-cinnolines analogue is by the represented compound of following general formula (3):
Wherein A be the O-Y group (Y is a hydrogen atom, the low alkyl group that can be replaced by phenyl, lower acyl or can protected amino-acid residue); B is a hydrogen atom, low alkyl group, or form the imino-of carbonyl or replacement with A; L is N-W or W-C-W '; Each is to have the low alkyl group that is selected from hydroxyl, lower alkoxy and phenyl substituent independently for W and W ', phenyl, carboxyl, lower alkoxycarbonyl or hydrogen atom; X is a low alkyl group, lower alkoxycarbonyl, rudimentary amido, lower alkoxy, trifluoromethyl, nitro, cyano group or halogen atom; X ' is a low alkyl group, lower alkoxycarbonyl, rudimentary amido, lower alkoxy, trifluoromethyl, nitro, cyano group, halogen atom or hydrogen atom; Each is 0 to 3 integer independently for m and q; And each is 0 or 1 independently for n and n '.
3. according to the antineoplastic agent of claim 2, wherein B is a hydrogen atom; L is W-C-W '; Each is to have low alkyl group or the hydrogen atom that is selected from hydroxyl, lower alkoxy and phenyl substituent independently for W and W '; X is the 3-trifluoromethyl, 3-nitro, 3-cyano group or 3-bromine group; X ' is a hydrogen atom; M and q are 1 separately respectively; N is 0 or 1; And n ' is 0.
4. according to the antineoplastic agent of claim 3, wherein W and W ' each be hydrogen atom or low alkyl group independently, and X is the 3-trifluoromethyl.
5. according to the antineoplastic agent of claim 2, wherein Y is the glycyl group, alanyl group, valyl group or α-Gu Anxianji group; B is a hydrogen atom; L is H-C-CH
3X is the 3-trifluoromethyl; X ' is a hydrogen atom; M and q are 1 separately respectively; N is 0 or 1; And n ' is 0.
6. according to the antineoplastic agent of claim 1, wherein 3-phenyl-cinnolines analogue is by the represented compound of following general formula (4):
Wherein X and X ' are low alkyl group independently of one another, lower alkoxycarbonyl, rudimentary amido, lower alkoxy, trifluoromethyl, nitro, cyano group, halogen atom or hydrogen atom; Y is the low alkyl group that can be replaced by phenyl, lower acyl or hydrogen atom; W can have the low alkyl group that is selected from hydroxyl, lower alkoxy and phenyl substituent, phenyl, carboxyl, lower alkoxycarbonyl or hydrogen atom.
7. according to the antineoplastic agent of claim 6, wherein X is a trifluoromethyl, nitro, cyano group or halogen atom; X ' is a hydrogen atom; W can have the low alkyl group that is selected from hydroxyl, lower alkoxy and phenyl substituent.
8. according to the antineoplastic agent of claim 7, wherein X is the 3-trifluoromethyl, 3-nitro, 3-cyano group or 3-halogen atom; W is the low alkyl group of non-replacement.
9. according to the antineoplastic agent of claim 1, wherein 3-phenyl-cinnolines analogue is by the represented compound of following general formula (5):
Wherein W and W ' are hydrogen atom or low alkyl group independently of one another; X is a junior alkyl halides; Z is Sauerstoffatom or N-Q; Q is amino, low-grade alkyl amino, hydroxyl or lower alkoxy.
10. according to the antineoplastic agent of claim 9, wherein W is hydrogen atom or methyl; W ' is hydrogen atom or methyl; X is the 3-trifluoromethyl; Z is a Sauerstoffatom.
11. according to the antineoplastic agent of claim 9, wherein W is hydrogen atom or methyl; W ' is hydrogen atom or methyl; X is the 3-trifluoromethyl; Z is N-NH
2
12. according to the antineoplastic agent of claim 1, wherein 3-phenyl cinnolines analogue is:
7-methyl-3-(3-trifluoromethyl)-7,8-dihydro-6H-cinnolines-5-ketone,
7-methyl-3-(3-trifluoromethyl)-5,6,7,8-tetrahydrochysene cinnolines-5-alcohol,
7-methyl-3-(3-trifluoromethyl) cinnolines-5-alcohol,
7-methyl isophthalic acid-oxygen base-3-(3-trifluoromethyl)-5,6,7,8-tetrahydrochysene cinnolines-5-alcohol,
5-glycyl oxygen base-7-methyl-3-(3-trifluoromethyl)-5,6,7,8-tetrahydrochysene cinnolines,
5-(L-alanyl) oxygen base-7-methyl-3-(3-trifluoromethyl)-5,6,7,8-tetrahydrochysene cinnolines,
5-(L-valyl) oxygen base-7-methyl-3-(3-trifluoromethyl)-5,6,7,8-tetrahydrochysene cinnolines,
5-(L-α-Gu Anxianji) oxygen base-7-methyl-3-(3-trifluoromethyl)-5,6,7,8-tetrahydrochysene cinnolines.
13. comprise according to claim 1-12 each 3-phenyl-cinnolines analogue or its physiology on acceptable salt as the inhibition of cell proliferation of active ingredient.
14. according to claim 1-12 each 3-phenyl-cinnolines analogue or its physiology on acceptable salt, condition is not comprise that wherein Z is the compound of Sauerstoffatom.
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