JPH01132568A - アロマターゼ阻害置換４（５）‐イミダゾール - Google Patents
アロマターゼ阻害置換４（５）‐イミダゾールInfo
- Publication number
- JPH01132568A JPH01132568A JP63254665A JP25466588A JPH01132568A JP H01132568 A JPH01132568 A JP H01132568A JP 63254665 A JP63254665 A JP 63254665A JP 25466588 A JP25466588 A JP 25466588A JP H01132568 A JPH01132568 A JP H01132568A
- Authority
- JP
- Japan
- Prior art keywords
- imidazole
- acid addition
- pharmacologically acceptable
- addition salt
- acceptable acid
- 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.)
- Pending
Links
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Substances C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 title claims description 106
- 102000014654 Aromatase Human genes 0.000 title description 10
- 108010078554 Aromatase Proteins 0.000 title description 10
- 230000002401 inhibitory effect Effects 0.000 title description 7
- 239000002253 acid Substances 0.000 claims abstract description 56
- 150000003839 salts Chemical class 0.000 claims abstract description 54
- 229940122815 Aromatase inhibitor Drugs 0.000 claims abstract description 5
- 239000003886 aromatase inhibitor Substances 0.000 claims abstract description 5
- 125000004450 alkenylene group Chemical group 0.000 claims abstract description 4
- 125000002947 alkylene group Chemical group 0.000 claims abstract description 4
- 150000001875 compounds Chemical class 0.000 claims description 93
- 231100000252 nontoxic Toxicity 0.000 claims description 51
- 230000003000 nontoxic effect Effects 0.000 claims description 51
- 239000000203 mixture Substances 0.000 claims description 37
- 125000005843 halogen group Chemical group 0.000 claims description 15
- 150000002460 imidazoles Chemical class 0.000 claims description 13
- 239000000126 substance Substances 0.000 claims description 7
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 6
- 239000004480 active ingredient Substances 0.000 claims description 3
- 125000004432 carbon atom Chemical group C* 0.000 claims description 3
- WYJDAFSFBUKHBD-UHFFFAOYSA-N 1,1-bis(4-chlorophenyl)-3-(1h-imidazol-5-yl)propan-1-ol Chemical compound C=1C=C(Cl)C=CC=1C(C=1C=CC(Cl)=CC=1)(O)CCC1=CNC=N1 WYJDAFSFBUKHBD-UHFFFAOYSA-N 0.000 claims description 2
- KITCWNRQRMFSAE-UHFFFAOYSA-N 1-benzyl-5-(3,3-diphenylpropyl)imidazole Chemical compound C=1C=CC=CC=1C(C=1C=CC=CC=1)CCC1=CN=CN1CC1=CC=CC=C1 KITCWNRQRMFSAE-UHFFFAOYSA-N 0.000 claims description 2
- ZOPVULSVIKGETK-UHFFFAOYSA-N 1-benzyl-5-[3,3-bis(4-methylphenyl)prop-1-en-2-yl]imidazole Chemical compound C1=CC(C)=CC=C1C(C=1C=CC(C)=CC=1)C(=C)C1=CN=CN1CC1=CC=CC=C1 ZOPVULSVIKGETK-UHFFFAOYSA-N 0.000 claims description 2
- YWZTXESYYIUWOO-UHFFFAOYSA-N 3-(3-benzylimidazol-4-yl)-1,1-bis(4-chlorophenyl)propan-1-ol Chemical compound C=1C=C(Cl)C=CC=1C(C=1C=CC(Cl)=CC=1)(O)CCC1=CN=CN1CC1=CC=CC=C1 YWZTXESYYIUWOO-UHFFFAOYSA-N 0.000 claims description 2
- XKRRHSSIBUFZPJ-UHFFFAOYSA-N 5-(3,3-diphenylpropyl)-1h-imidazole Chemical compound C=1C=CC=CC=1C(C=1C=CC=CC=1)CCC1=CNC=N1 XKRRHSSIBUFZPJ-UHFFFAOYSA-N 0.000 claims description 2
- LKPKZUIBNIUCLS-UHFFFAOYSA-N 5-[3,3-bis(2,3-dimethylphenyl)propyl]-1h-imidazole Chemical compound CC1=CC=CC(C(CCC=2N=CNC=2)C=2C(=C(C)C=CC=2)C)=C1C LKPKZUIBNIUCLS-UHFFFAOYSA-N 0.000 claims description 2
- PDWYNTGEHDMBCC-UHFFFAOYSA-N 5-[3,3-bis(3-fluorophenyl)prop-1-en-2-yl]-1h-imidazole Chemical compound FC1=CC=CC(C(C(=C)C=2N=CNC=2)C=2C=C(F)C=CC=2)=C1 PDWYNTGEHDMBCC-UHFFFAOYSA-N 0.000 claims description 2
- YKODNVUQJCBYIA-UHFFFAOYSA-N 5-[3,3-bis(3-methoxyphenyl)propyl]-1h-imidazole Chemical compound COC1=CC=CC(C(CCC=2N=CNC=2)C=2C=C(OC)C=CC=2)=C1 YKODNVUQJCBYIA-UHFFFAOYSA-N 0.000 claims description 2
- GBXOEZIBSXRVMX-UHFFFAOYSA-N 5-[3,3-bis(3-methylphenyl)prop-1-en-2-yl]-1h-imidazole Chemical compound CC1=CC=CC(C(C(=C)C=2N=CNC=2)C=2C=C(C)C=CC=2)=C1 GBXOEZIBSXRVMX-UHFFFAOYSA-N 0.000 claims description 2
- CSYRBPPNVKZGHD-UHFFFAOYSA-N 5-[3,3-bis(3-methylphenyl)propyl]-1h-imidazole Chemical compound CC1=CC=CC(C(CCC=2N=CNC=2)C=2C=C(C)C=CC=2)=C1 CSYRBPPNVKZGHD-UHFFFAOYSA-N 0.000 claims description 2
- MMFCVWVKQOXREF-UHFFFAOYSA-N 5-[5-(2,6-dimethylphenyl)-3-[2-(2,6-dimethylphenyl)ethyl]pentyl]-1h-imidazole Chemical compound CC1=CC=CC(C)=C1CCC(CCC=1C(=CC=CC=1C)C)CCC1=CNC=N1 MMFCVWVKQOXREF-UHFFFAOYSA-N 0.000 claims description 2
- 125000001424 substituent group Chemical group 0.000 claims description 2
- ZNOZFEFFMRMISV-UHFFFAOYSA-N 5-[3,3-bis(3,5-dimethylphenyl)propyl]-1h-imidazole Chemical compound CC1=CC(C)=CC(C(CCC=2N=CNC=2)C=2C=C(C)C=C(C)C=2)=C1 ZNOZFEFFMRMISV-UHFFFAOYSA-N 0.000 claims 2
- OHQSOQNRQQLRMX-UHFFFAOYSA-N 1-(3-benzylimidazol-4-yl)-5-(2,6-dimethylphenyl)-3-[2-(2,6-dimethylphenyl)ethyl]pentan-3-ol Chemical compound CC1=CC=CC(C)=C1CCC(O)(CCC=1C(=CC=CC=1C)C)CCC1=CN=CN1CC1=CC=CC=C1 OHQSOQNRQQLRMX-UHFFFAOYSA-N 0.000 claims 1
- GUDQPRHRGNSLRL-UHFFFAOYSA-N 1-(4-chlorophenyl)-3-(1h-imidazol-5-yl)-1-phenylpropan-1-ol Chemical compound C=1C=CC=CC=1C(C=1C=CC(Cl)=CC=1)(O)CCC1=CNC=N1 GUDQPRHRGNSLRL-UHFFFAOYSA-N 0.000 claims 1
- OSEXTGSEVIILPG-UHFFFAOYSA-N 1-[(4-chlorophenyl)methyl]-4-(3,3-diphenylpropyl)imidazole Chemical compound C1=CC(Cl)=CC=C1CN1C=C(CCC(C=2C=CC=CC=2)C=2C=CC=CC=2)N=C1 OSEXTGSEVIILPG-UHFFFAOYSA-N 0.000 claims 1
- RYFDLXUXRKVOJC-UHFFFAOYSA-N 1-[(4-chlorophenyl)methyl]-5-(3,3-diphenylpropyl)imidazole Chemical compound C1=CC(Cl)=CC=C1CN1C(CCC(C=2C=CC=CC=2)C=2C=CC=CC=2)=CN=C1 RYFDLXUXRKVOJC-UHFFFAOYSA-N 0.000 claims 1
- CXLNHKYZUZFCKL-UHFFFAOYSA-N 1-benzyl-4-(3,3-diphenylpropyl)imidazole Chemical compound C=1C=CC=CC=1C(C=1C=CC=CC=1)CCC(N=C1)=CN1CC1=CC=CC=C1 CXLNHKYZUZFCKL-UHFFFAOYSA-N 0.000 claims 1
- ZYOUMQWMXFAETM-UHFFFAOYSA-N 1-benzyl-5-(3,3-diphenylprop-1-en-2-yl)imidazole Chemical compound C=1N=CN(CC=2C=CC=CC=2)C=1C(=C)C(C=1C=CC=CC=1)C1=CC=CC=C1 ZYOUMQWMXFAETM-UHFFFAOYSA-N 0.000 claims 1
- BBPTYKAKTBSNRQ-UHFFFAOYSA-N 1-benzyl-5-[3,3-bis(2,3-dimethylphenyl)prop-1-en-2-yl]imidazole Chemical compound CC1=CC=CC(C(C(=C)C=2N(C=NC=2)CC=2C=CC=CC=2)C=2C(=C(C)C=CC=2)C)=C1C BBPTYKAKTBSNRQ-UHFFFAOYSA-N 0.000 claims 1
- MJXVXODZMLCPEZ-UHFFFAOYSA-N 1-benzyl-5-[3,3-bis(2-methoxyphenyl)prop-1-en-2-yl]imidazole Chemical compound COC1=CC=CC=C1C(C=1C(=CC=CC=1)OC)C(=C)C1=CN=CN1CC1=CC=CC=C1 MJXVXODZMLCPEZ-UHFFFAOYSA-N 0.000 claims 1
- KUQVWXWUUFZXBK-UHFFFAOYSA-N 1-benzyl-5-[3,3-bis(2-methylphenyl)prop-1-en-2-yl]imidazole Chemical compound CC1=CC=CC=C1C(C=1C(=CC=CC=1)C)C(=C)C1=CN=CN1CC1=CC=CC=C1 KUQVWXWUUFZXBK-UHFFFAOYSA-N 0.000 claims 1
- UMKRYUCVOUULJF-UHFFFAOYSA-N 1-benzyl-5-[3,3-bis(3,5-dimethylphenyl)prop-1-en-2-yl]imidazole Chemical compound CC1=CC(C)=CC(C(C(=C)C=2N(C=NC=2)CC=2C=CC=CC=2)C=2C=C(C)C=C(C)C=2)=C1 UMKRYUCVOUULJF-UHFFFAOYSA-N 0.000 claims 1
- UMQSCRPJAQXVCZ-UHFFFAOYSA-N 1-benzyl-5-[3,3-bis(3-methoxyphenyl)prop-1-en-2-yl]imidazole Chemical compound COC1=CC=CC(C(C(=C)C=2N(C=NC=2)CC=2C=CC=CC=2)C=2C=C(OC)C=CC=2)=C1 UMQSCRPJAQXVCZ-UHFFFAOYSA-N 0.000 claims 1
- GROIQLCDBZPASZ-UHFFFAOYSA-N 1-benzyl-5-[3,3-bis(3-methoxyphenyl)propyl]imidazole Chemical compound COC1=CC=CC(C(CCC=2N(C=NC=2)CC=2C=CC=CC=2)C=2C=C(OC)C=CC=2)=C1 GROIQLCDBZPASZ-UHFFFAOYSA-N 0.000 claims 1
- UOQDMVIYXDRYFS-UHFFFAOYSA-N 1-benzyl-5-[3,3-bis(3-methylphenyl)prop-1-en-2-yl]imidazole Chemical compound CC1=CC=CC(C(C(=C)C=2N(C=NC=2)CC=2C=CC=CC=2)C=2C=C(C)C=CC=2)=C1 UOQDMVIYXDRYFS-UHFFFAOYSA-N 0.000 claims 1
- AUFUORKXLQNQNB-UHFFFAOYSA-N 1-benzyl-5-[3,3-bis(4-chlorophenyl)prop-1-en-2-yl]imidazole Chemical compound C1=CC(Cl)=CC=C1C(C=1C=CC(Cl)=CC=1)C(=C)C1=CN=CN1CC1=CC=CC=C1 AUFUORKXLQNQNB-UHFFFAOYSA-N 0.000 claims 1
- BUZDXPJHMXJXGX-UHFFFAOYSA-N 1-benzyl-5-[3,3-bis(4-methoxyphenyl)prop-1-en-2-yl]imidazole Chemical compound C1=CC(OC)=CC=C1C(C=1C=CC(OC)=CC=1)C(=C)C1=CN=CN1CC1=CC=CC=C1 BUZDXPJHMXJXGX-UHFFFAOYSA-N 0.000 claims 1
- UPYVYJSWGZMBOU-UHFFFAOYSA-N 1-pentylimidazole Chemical compound CCCCCN1C=CN=C1 UPYVYJSWGZMBOU-UHFFFAOYSA-N 0.000 claims 1
- COQXXUZCXSXXJW-UHFFFAOYSA-N 3-(1h-imidazol-5-yl)-1,1-bis(2-methylphenyl)propan-1-ol Chemical compound CC1=CC=CC=C1C(O)(C=1C(=CC=CC=1)C)CCC1=CNC=N1 COQXXUZCXSXXJW-UHFFFAOYSA-N 0.000 claims 1
- SNDWLQJLXVTFOH-UHFFFAOYSA-N 3-(1h-imidazol-5-yl)-1,1-diphenylpropan-1-ol Chemical compound C=1C=CC=CC=1C(C=1C=CC=CC=1)(O)CCC1=CNC=N1 SNDWLQJLXVTFOH-UHFFFAOYSA-N 0.000 claims 1
- LOMUAEFYLMDOBR-UHFFFAOYSA-N 5-[3,3-bis(2-methoxyphenyl)propyl]-1h-imidazole Chemical compound COC1=CC=CC=C1C(C=1C(=CC=CC=1)OC)CCC1=CNC=N1 LOMUAEFYLMDOBR-UHFFFAOYSA-N 0.000 claims 1
- NAMOLCGELAJGEK-UHFFFAOYSA-N 5-[3,3-bis(2-methylphenyl)prop-1-en-2-yl]-1h-imidazole Chemical compound CC1=CC=CC=C1C(C=1C(=CC=CC=1)C)C(=C)C1=CNC=N1 NAMOLCGELAJGEK-UHFFFAOYSA-N 0.000 claims 1
- QZBYGBAZOZHGFB-UHFFFAOYSA-N 5-[3,3-bis(2-methylphenyl)propyl]-1h-imidazole Chemical compound CC1=CC=CC=C1C(C=1C(=CC=CC=1)C)CCC1=CNC=N1 QZBYGBAZOZHGFB-UHFFFAOYSA-N 0.000 claims 1
- GDHZTEVCCIBMLZ-UHFFFAOYSA-N 5-[3,3-bis(3-fluorophenyl)propyl]-1h-imidazole Chemical compound FC1=CC=CC(C(CCC=2N=CNC=2)C=2C=C(F)C=CC=2)=C1 GDHZTEVCCIBMLZ-UHFFFAOYSA-N 0.000 claims 1
- SWERYUFJIDDFCR-UHFFFAOYSA-N 5-[3,3-bis(4-chlorophenyl)prop-1-en-2-yl]-1h-imidazole Chemical compound C1=CC(Cl)=CC=C1C(C=1C=CC(Cl)=CC=1)C(=C)C1=CNC=N1 SWERYUFJIDDFCR-UHFFFAOYSA-N 0.000 claims 1
- GNCKACFWLLJVLO-UHFFFAOYSA-N 5-[3,3-bis(4-methoxyphenyl)propyl]-1h-imidazole Chemical compound C1=CC(OC)=CC=C1C(C=1C=CC(OC)=CC=1)CCC1=CNC=N1 GNCKACFWLLJVLO-UHFFFAOYSA-N 0.000 claims 1
- KWVUAYDFDNWYEX-UHFFFAOYSA-N 5-[3,3-bis(4-methylphenyl)propyl]-1h-imidazole Chemical compound C1=CC(C)=CC=C1C(C=1C=CC(C)=CC=1)CCC1=CNC=N1 KWVUAYDFDNWYEX-UHFFFAOYSA-N 0.000 claims 1
- 238000000034 method Methods 0.000 abstract description 16
- 229940011871 estrogen Drugs 0.000 abstract description 12
- 239000000262 estrogen Substances 0.000 abstract description 12
- 206010006187 Breast cancer Diseases 0.000 abstract description 7
- 208000026310 Breast neoplasm Diseases 0.000 abstract description 7
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 abstract description 6
- 230000001419 dependent effect Effects 0.000 abstract description 5
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract description 4
- 201000010099 disease Diseases 0.000 abstract description 3
- 230000000843 anti-fungal effect Effects 0.000 abstract description 2
- 230000001857 anti-mycotic effect Effects 0.000 abstract description 2
- 239000002543 antimycotic Substances 0.000 abstract description 2
- 229910052736 halogen Inorganic materials 0.000 abstract 2
- 150000002367 halogens Chemical class 0.000 abstract 2
- MDFFNEOEWAXZRQ-UHFFFAOYSA-N aminyl Chemical compound [NH2] MDFFNEOEWAXZRQ-UHFFFAOYSA-N 0.000 abstract 1
- CBOIHMRHGLHBPB-UHFFFAOYSA-N hydroxymethyl Chemical compound O[CH2] CBOIHMRHGLHBPB-UHFFFAOYSA-N 0.000 abstract 1
- 239000000463 material Substances 0.000 abstract 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 abstract 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 50
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 42
- 238000002844 melting Methods 0.000 description 33
- 230000008018 melting Effects 0.000 description 33
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 31
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 29
- 238000006243 chemical reaction Methods 0.000 description 29
- 239000000047 product Substances 0.000 description 26
- 239000011541 reaction mixture Substances 0.000 description 26
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 24
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 21
- 238000004458 analytical method Methods 0.000 description 20
- 239000002585 base Substances 0.000 description 20
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 19
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 18
- 239000000243 solution Substances 0.000 description 17
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 15
- -1 R3 represents -11 Chemical group 0.000 description 15
- 238000004519 manufacturing process Methods 0.000 description 15
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 12
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 12
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 12
- 229910052739 hydrogen Inorganic materials 0.000 description 12
- 239000001257 hydrogen Substances 0.000 description 12
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 11
- 238000002360 preparation method Methods 0.000 description 11
- 238000003747 Grignard reaction Methods 0.000 description 10
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 10
- 238000005984 hydrogenation reaction Methods 0.000 description 10
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 9
- 238000012360 testing method Methods 0.000 description 8
- QCQCHGYLTSGIGX-GHXANHINSA-N 4-[[(3ar,5ar,5br,7ar,9s,11ar,11br,13as)-5a,5b,8,8,11a-pentamethyl-3a-[(5-methylpyridine-3-carbonyl)amino]-2-oxo-1-propan-2-yl-4,5,6,7,7a,9,10,11,11b,12,13,13a-dodecahydro-3h-cyclopenta[a]chrysen-9-yl]oxy]-2,2-dimethyl-4-oxobutanoic acid Chemical compound N([C@@]12CC[C@@]3(C)[C@]4(C)CC[C@H]5C(C)(C)[C@@H](OC(=O)CC(C)(C)C(O)=O)CC[C@]5(C)[C@H]4CC[C@@H]3C1=C(C(C2)=O)C(C)C)C(=O)C1=CN=CC(C)=C1 QCQCHGYLTSGIGX-GHXANHINSA-N 0.000 description 7
- 150000004795 grignard reagents Chemical class 0.000 description 7
- 239000002244 precipitate Substances 0.000 description 7
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 6
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 6
- 239000007818 Grignard reagent Substances 0.000 description 6
- 239000003054 catalyst Substances 0.000 description 6
- 239000011777 magnesium Substances 0.000 description 6
- 229910052749 magnesium Inorganic materials 0.000 description 6
- 239000002904 solvent Substances 0.000 description 6
- 102000004190 Enzymes Human genes 0.000 description 5
- 108090000790 Enzymes Proteins 0.000 description 5
- QARVLSVVCXYDNA-UHFFFAOYSA-N bromobenzene Chemical compound BrC1=CC=CC=C1 QARVLSVVCXYDNA-UHFFFAOYSA-N 0.000 description 5
- 150000004820 halides Chemical class 0.000 description 5
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 5
- CHKVPAROMQMJNQ-UHFFFAOYSA-M potassium bisulfate Chemical compound [K+].OS([O-])(=O)=O CHKVPAROMQMJNQ-UHFFFAOYSA-M 0.000 description 5
- 229910000343 potassium bisulfate Inorganic materials 0.000 description 5
- 239000007858 starting material Substances 0.000 description 5
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 4
- 229910002651 NO3 Inorganic materials 0.000 description 4
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 4
- 230000002378 acidificating effect Effects 0.000 description 4
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 4
- 229910052799 carbon Inorganic materials 0.000 description 4
- 239000000969 carrier Substances 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- IDGUHHHQCWSQLU-UHFFFAOYSA-N ethanol;hydrate Chemical compound O.CCO IDGUHHHQCWSQLU-UHFFFAOYSA-N 0.000 description 4
- 150000008282 halocarbons Chemical class 0.000 description 4
- 230000005764 inhibitory process Effects 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 238000009835 boiling Methods 0.000 description 3
- 230000003197 catalytic effect Effects 0.000 description 3
- 230000018044 dehydration Effects 0.000 description 3
- 238000006297 dehydration reaction Methods 0.000 description 3
- 239000003814 drug Substances 0.000 description 3
- 239000000706 filtrate Substances 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 210000000056 organ Anatomy 0.000 description 3
- 239000008194 pharmaceutical composition Substances 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- 238000003786 synthesis reaction Methods 0.000 description 3
- HFIPDASZGMVXNQ-UHFFFAOYSA-N 1-(4-chlorophenyl)-4-(1h-imidazol-5-yl)butan-1-one Chemical compound C1=CC(Cl)=CC=C1C(=O)CCCC1=CN=CN1 HFIPDASZGMVXNQ-UHFFFAOYSA-N 0.000 description 2
- NHDODQWIKUYWMW-UHFFFAOYSA-N 1-bromo-4-chlorobenzene Chemical compound ClC1=CC=C(Br)C=C1 NHDODQWIKUYWMW-UHFFFAOYSA-N 0.000 description 2
- VOXZDWNPVJITMN-ZBRFXRBCSA-N 17β-estradiol Chemical compound OC1=CC=C2[C@H]3CC[C@](C)([C@H](CC4)O)[C@@H]4[C@@H]3CCC2=C1 VOXZDWNPVJITMN-ZBRFXRBCSA-N 0.000 description 2
- 125000004180 3-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(F)=C1[H] 0.000 description 2
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- ANRQGKOBLBYXFM-UHFFFAOYSA-M phenylmagnesium bromide Chemical compound Br[Mg]C1=CC=CC=C1 ANRQGKOBLBYXFM-UHFFFAOYSA-M 0.000 description 1
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/56—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/10—Antimycotics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/64—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms, e.g. histidine
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Public Health (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB8723715 | 1987-10-09 | ||
| GB8723715A GB2210875B (en) | 1987-10-09 | 1987-10-09 | Aromatase inhibiting 4(5)-imidazoles |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH01132568A true JPH01132568A (ja) | 1989-05-25 |
Family
ID=10625036
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP63254665A Pending JPH01132568A (ja) | 1987-10-09 | 1988-10-08 | アロマターゼ阻害置換４（５）‐イミダゾール |
Country Status (24)
Families Citing this family (31)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB2210875B (en) | 1987-10-09 | 1991-05-29 | Farmos Oy | Aromatase inhibiting 4(5)-imidazoles |
| GB8818561D0 (en) * | 1988-08-04 | 1988-09-07 | Ici Plc | Diphenylethane derivatives |
| US5439928A (en) * | 1989-03-30 | 1995-08-08 | Orion-Yhtyma Oy | Aromatase inhibiting 4(5)-imidazoles |
| GB2248058B (en) * | 1990-09-21 | 1994-09-14 | Orion Yhtymae Oy | Aromatase inhibiting 4(5)-imidazoles |
| GB2229719B (en) * | 1989-03-30 | 1992-04-29 | Farmos Oy | Novel aromatase inhibiting 4(5)-imidazoles |
| AU627559B2 (en) * | 1989-03-30 | 1992-08-27 | Farmos-Yhtyma Oy | Novel aromatase inhibiting 4(5)-imidazoles |
| GB9125924D0 (en) * | 1991-06-18 | 1992-02-05 | Orion Yhtymae Oy | Stereoisomers of an imidazole derivative |
| ZA962879B (en) * | 1995-04-12 | 1997-03-17 | Procter & Gamble | A pharmaceutical composition for inhibiting the growth of viruses and cancers |
| US6262093B1 (en) | 1995-04-12 | 2001-07-17 | The Proctor & Gamble Company | Methods of treating cancer with benzimidazoles |
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| US5900429A (en) * | 1997-01-28 | 1999-05-04 | The Procter & Gamble Company | Method for inhibiting the growth of cancers |
| US6506783B1 (en) | 1997-05-16 | 2003-01-14 | The Procter & Gamble Company | Cancer treatments and pharmaceutical compositions therefor |
| US6245789B1 (en) | 1998-05-19 | 2001-06-12 | The Procter & Gamble Company | HIV and viral treatment |
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| US6380232B1 (en) | 2000-09-26 | 2002-04-30 | The Procter & Gamble Company | Benzimidazole urea derivatives, and pharmaceutical compositions and unit dosages thereof |
| US6515074B2 (en) * | 2001-01-22 | 2003-02-04 | Delphi Technologies, Inc. | Thermoplastic polymer alloy compositions and process for manufacture thereof |
| WO2003082787A1 (en) * | 2002-03-26 | 2003-10-09 | Boehringer Ingelheim Pharmaceuticals, Inc. | Glucocorticoid mimetics, methods of making them, pharmaceutical compositions, and uses thereof |
| ES2298508T3 (es) | 2002-03-26 | 2008-05-16 | Boehringer Ingelheim Pharmaceuticals Inc. | Mimeticos de glucocorticoides, metodos para prepararlos, composiciones farmaceuticas y sus usos. |
| US7074806B2 (en) | 2002-06-06 | 2006-07-11 | Boehringer Ingelheim Pharmaceuticals, Inc. | Glucocorticoid mimetics, methods of making them, pharmaceutical compositions, and uses thereof |
| WO2004063163A1 (en) | 2003-01-03 | 2004-07-29 | Boehringer Ingelheim Pharmaceuticals, Inc. | 1-propanol and 1-propylamine derivatives and their use as glucocorticoid ligands |
| UY28526A1 (es) | 2003-09-24 | 2005-04-29 | Boehringer Ingelheim Pharma | Miméticos de glucocorticoides, métodos de preparación composiciones farmacéuticas y usos de los mismos |
| US7795272B2 (en) | 2004-03-13 | 2010-09-14 | Boehringer Ingelheim Pharmaceutical, Inc. | Glucocorticoid mimetics, methods of making them, pharmaceutical compositions and uses thereof |
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Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB2069481B (en) * | 1980-02-13 | 1983-07-27 | Farmos Oy | Substituted imidazole derivatives |
| GB2092569B (en) * | 1981-02-05 | 1984-09-19 | Farmos Oy | Substituted imidazole derivatives and their preparation and use |
| GB2096987B (en) * | 1981-04-22 | 1984-04-04 | Farmos Oy | Substituted imidazole and imidazole derivatives and their preparation and use |
| GB2101114B (en) * | 1981-07-10 | 1985-05-22 | Farmos Group Ltd | Substituted imidazole derivatives and their preparation and use |
| US4605661A (en) * | 1984-06-18 | 1986-08-12 | Eli Lilly And Company | Aromastase inhibiting α,α-diarylimidazole-4(5)-propionitriles, α,α-diarylimidazole-4(5)-propionamides, and 4(5)-(2,2-diarylethyl)imidazoles |
| LU85747A1 (fr) * | 1985-01-28 | 1986-08-04 | Continental Pharma | Derives d'imidazole leur preparation et utilisation ainsi que les compositions pharmaceutiques contenant des derives |
| GB2210875B (en) | 1987-10-09 | 1991-05-29 | Farmos Oy | Aromatase inhibiting 4(5)-imidazoles |
| AU627559B2 (en) | 1989-03-30 | 1992-08-27 | Farmos-Yhtyma Oy | Novel aromatase inhibiting 4(5)-imidazoles |
-
1987
- 1987-10-09 GB GB8723715A patent/GB2210875B/en not_active Revoked
-
1988
- 1988-09-22 CA CA000578192A patent/CA1329616C/en not_active Expired - Fee Related
- 1988-09-30 FI FI884497A patent/FI93105C/fi not_active IP Right Cessation
- 1988-10-03 DK DK550988A patent/DK550988A/da not_active Application Discontinuation
- 1988-10-06 DD DD88320542A patent/DD282912A5/de not_active IP Right Cessation
- 1988-10-06 AU AU23490/88A patent/AU615482B2/en not_active Ceased
- 1988-10-06 NZ NZ226483A patent/NZ226483A/xx unknown
- 1988-10-07 ES ES88309413T patent/ES2043839T3/es not_active Expired - Lifetime
- 1988-10-07 DE DE8888309413T patent/DE3874073T2/de not_active Expired - Fee Related
- 1988-10-07 PT PT88717A patent/PT88717B/pt not_active IP Right Cessation
- 1988-10-07 IE IE305588A patent/IE61180B1/en not_active IP Right Cessation
- 1988-10-07 EP EP88309413A patent/EP0311447B1/en not_active Expired - Lifetime
- 1988-10-07 NO NO884473A patent/NO172048C/no unknown
- 1988-10-07 UA UA4356681A patent/UA13218A/uk unknown
- 1988-10-07 ZA ZA887545A patent/ZA887545B/xx unknown
- 1988-10-07 RU SU884356681A patent/RU1819263C/ru active
- 1988-10-07 IL IL87969A patent/IL87969A/xx not_active IP Right Cessation
- 1988-10-07 HU HU885213A patent/HU201024B/hu not_active IP Right Cessation
- 1988-10-08 KR KR1019880013196A patent/KR890006593A/ko not_active Application Discontinuation
- 1988-10-08 JP JP63254665A patent/JPH01132568A/ja active Pending
- 1988-10-08 CN CN88108425A patent/CN1036993C/zh not_active Expired - Fee Related
-
1990
- 1990-09-27 US US07/588,873 patent/US5098923A/en not_active Expired - Fee Related
-
1992
- 1992-01-23 RU SU925010700A patent/RU2045519C1/ru active
- 1992-11-26 GR GR920402701T patent/GR3006343T3/el unknown
-
1993
- 1993-08-31 LT LTIP916A patent/LT3658B/lt not_active IP Right Cessation
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