DE602004008300T2 - Thiazolinderivate als selektive androgenrezeptormodulatoren (sarms) - Google Patents
Thiazolinderivate als selektive androgenrezeptormodulatoren (sarms) Download PDFInfo
- Publication number
- DE602004008300T2 DE602004008300T2 DE602004008300T DE602004008300T DE602004008300T2 DE 602004008300 T2 DE602004008300 T2 DE 602004008300T2 DE 602004008300 T DE602004008300 T DE 602004008300T DE 602004008300 T DE602004008300 T DE 602004008300T DE 602004008300 T2 DE602004008300 T2 DE 602004008300T2
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- Prior art keywords
- alkyl
- group
- hydrogen
- chlorophenyl
- mmol
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
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- 150000003549 thiazolines Chemical class 0.000 title abstract description 4
- 239000000849 selective androgen receptor modulator Substances 0.000 title description 4
- 102000001307 androgen receptors Human genes 0.000 claims abstract description 17
- 108010080146 androgen receptors Proteins 0.000 claims abstract description 17
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims abstract description 10
- 239000008194 pharmaceutical composition Substances 0.000 claims abstract description 10
- 208000035475 disorder Diseases 0.000 claims abstract description 9
- 150000001875 compounds Chemical class 0.000 claims description 81
- 125000000217 alkyl group Chemical group 0.000 claims description 80
- -1 hydroxy, carboxy Chemical group 0.000 claims description 58
- 229910052739 hydrogen Inorganic materials 0.000 claims description 47
- 239000001257 hydrogen Substances 0.000 claims description 47
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 34
- 125000001424 substituent group Chemical group 0.000 claims description 33
- 125000003118 aryl group Chemical group 0.000 claims description 28
- 125000001072 heteroaryl group Chemical group 0.000 claims description 19
- 238000000034 method Methods 0.000 claims description 18
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 18
- 150000002431 hydrogen Chemical class 0.000 claims description 13
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 13
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 12
- 125000003545 alkoxy group Chemical group 0.000 claims description 11
- 125000001889 triflyl group Chemical group FC(F)(F)S(*)(=O)=O 0.000 claims description 11
- 125000003282 alkyl amino group Chemical group 0.000 claims description 10
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 10
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 10
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 claims description 8
- 150000003839 salts Chemical class 0.000 claims description 8
- 239000003814 drug Substances 0.000 claims description 7
- 229910052736 halogen Inorganic materials 0.000 claims description 7
- 150000002367 halogens Chemical class 0.000 claims description 7
- 206010020112 Hirsutism Diseases 0.000 claims description 6
- 206010060862 Prostate cancer Diseases 0.000 claims description 6
- 125000001188 haloalkyl group Chemical group 0.000 claims description 6
- 125000001255 4-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1F 0.000 claims description 5
- 208000030507 AIDS Diseases 0.000 claims description 5
- 208000002874 Acne Vulgaris Diseases 0.000 claims description 5
- 201000004384 Alopecia Diseases 0.000 claims description 5
- 208000000103 Anorexia Nervosa Diseases 0.000 claims description 5
- 206010006187 Breast cancer Diseases 0.000 claims description 5
- 208000026310 Breast neoplasm Diseases 0.000 claims description 5
- 206010006895 Cachexia Diseases 0.000 claims description 5
- 239000002253 acid Substances 0.000 claims description 5
- 206010000496 acne Diseases 0.000 claims description 5
- 231100000360 alopecia Toxicity 0.000 claims description 5
- 238000004519 manufacturing process Methods 0.000 claims description 5
- 125000004179 3-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(Cl)=C1[H] 0.000 claims description 4
- 229910052799 carbon Inorganic materials 0.000 claims description 4
- 238000002156 mixing Methods 0.000 claims description 4
- 201000001514 prostate carcinoma Diseases 0.000 claims description 4
- 125000004432 carbon atom Chemical group C* 0.000 claims description 3
- 238000002360 preparation method Methods 0.000 claims description 3
- 230000008569 process Effects 0.000 claims description 3
- 125000004801 4-cyanophenyl group Chemical group [H]C1=C([H])C(C#N)=C([H])C([H])=C1* 0.000 claims description 2
- 239000003937 drug carrier Substances 0.000 claims description 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 2
- 125000001475 halogen functional group Chemical group 0.000 claims 7
- 125000004769 (C1-C4) alkylsulfonyl group Chemical class 0.000 claims 1
- 229940079593 drug Drugs 0.000 claims 1
- 230000001404 mediated effect Effects 0.000 claims 1
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 149
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical class CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 117
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 95
- 239000012043 crude product Substances 0.000 description 75
- 235000019439 ethyl acetate Nutrition 0.000 description 74
- 239000011541 reaction mixture Substances 0.000 description 71
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 67
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 58
- VHYFNPMBLIVWCW-UHFFFAOYSA-N 4-Dimethylaminopyridine Chemical compound CN(C)C1=CC=NC=C1 VHYFNPMBLIVWCW-UHFFFAOYSA-N 0.000 description 56
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 55
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 53
- 239000000243 solution Substances 0.000 description 47
- 239000011734 sodium Substances 0.000 description 45
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 39
- 238000004440 column chromatography Methods 0.000 description 39
- 239000000706 filtrate Substances 0.000 description 39
- 239000000741 silica gel Substances 0.000 description 39
- 229910002027 silica gel Inorganic materials 0.000 description 39
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 38
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 34
- 239000012267 brine Substances 0.000 description 33
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 33
- 239000002274 desiccant Substances 0.000 description 32
- 229960000549 4-dimethylaminophenol Drugs 0.000 description 28
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 27
- 239000010410 layer Substances 0.000 description 27
- 238000005160 1H NMR spectroscopy Methods 0.000 description 26
- 239000012044 organic layer Substances 0.000 description 21
- 239000000203 mixture Substances 0.000 description 19
- 239000000284 extract Substances 0.000 description 14
- JGFZNNIVVJXRND-UHFFFAOYSA-N N,N-Diisopropylethylamine (DIPEA) Chemical compound CCN(C(C)C)C(C)C JGFZNNIVVJXRND-UHFFFAOYSA-N 0.000 description 13
- HCBROVLUPHEPFU-UHFFFAOYSA-N 2-(4-chlorophenyl)-4,5-dihydro-1,3-thiazole-4-carboxylic acid Chemical compound OC(=O)C1CSC(C=2C=CC(Cl)=CC=2)=N1 HCBROVLUPHEPFU-UHFFFAOYSA-N 0.000 description 12
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N DMSO Substances CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 12
- 125000005843 halogen group Chemical group 0.000 description 12
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 9
- FPXBJUKJASCWON-UHFFFAOYSA-N 2-(4-fluorophenyl)-5,5-dimethyl-4h-1,3-thiazole-4-carboxylic acid Chemical compound OC(=O)C1C(C)(C)SC(C=2C=CC(F)=CC=2)=N1 FPXBJUKJASCWON-UHFFFAOYSA-N 0.000 description 8
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 8
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 8
- MUMGGOZAMZWBJJ-DYKIIFRCSA-N Testostosterone Chemical compound O=C1CC[C@]2(C)[C@H]3CC[C@](C)([C@H](CC4)O)[C@@H]4[C@@H]3CCC2=C1 MUMGGOZAMZWBJJ-DYKIIFRCSA-N 0.000 description 8
- 239000003098 androgen Substances 0.000 description 8
- SKRDSZIZFIAERJ-UHFFFAOYSA-N 2-(3-chlorophenyl)-4,5-dihydro-1,3-thiazole-4-carboxylic acid Chemical compound OC(=O)C1CSC(C=2C=C(Cl)C=CC=2)=N1 SKRDSZIZFIAERJ-UHFFFAOYSA-N 0.000 description 7
- 238000005481 NMR spectroscopy Methods 0.000 description 7
- DLWLSGLANIMDOS-UHFFFAOYSA-N 2-(4-chlorophenyl)-n-[4-cyano-3-(trifluoromethyl)phenyl]-4,5-dihydro-1,3-thiazole-4-carboxamide Chemical compound C1=C(C#N)C(C(F)(F)F)=CC(NC(=O)C2N=C(SC2)C=2C=CC(Cl)=CC=2)=C1 DLWLSGLANIMDOS-UHFFFAOYSA-N 0.000 description 6
- QLFHGXSDTKGZDY-UHFFFAOYSA-N 2-(4-fluorophenyl)-4,5-dihydro-1,3-thiazole-4-carboxylic acid Chemical compound OC(=O)C1CSC(C=2C=CC(F)=CC=2)=N1 QLFHGXSDTKGZDY-UHFFFAOYSA-N 0.000 description 6
- PMDYLCUKSLBUHO-UHFFFAOYSA-N 4-amino-2-(trifluoromethyl)benzonitrile Chemical compound NC1=CC=C(C#N)C(C(F)(F)F)=C1 PMDYLCUKSLBUHO-UHFFFAOYSA-N 0.000 description 6
- 206010004446 Benign prostatic hyperplasia Diseases 0.000 description 6
- 208000004403 Prostatic Hyperplasia Diseases 0.000 description 6
- 239000005557 antagonist Substances 0.000 description 6
- 230000000694 effects Effects 0.000 description 6
- IUYHWZFSGMZEOG-UHFFFAOYSA-M magnesium;propane;chloride Chemical compound [Mg+2].[Cl-].C[CH-]C IUYHWZFSGMZEOG-UHFFFAOYSA-M 0.000 description 6
- 239000000047 product Substances 0.000 description 6
- 238000000746 purification Methods 0.000 description 6
- 210000001519 tissue Anatomy 0.000 description 6
- VERCSPMYPSZPLJ-UHFFFAOYSA-N 2-(4-chlorophenyl)-5,5-dimethyl-4h-1,3-thiazole-4-carboxylic acid Chemical compound OC(=O)C1C(C)(C)SC(C=2C=CC(Cl)=CC=2)=N1 VERCSPMYPSZPLJ-UHFFFAOYSA-N 0.000 description 5
- UTKUVRNVYFTEHF-UHFFFAOYSA-N 4-nitro-3-(trifluoromethyl)aniline Chemical compound NC1=CC=C([N+]([O-])=O)C(C(F)(F)F)=C1 UTKUVRNVYFTEHF-UHFFFAOYSA-N 0.000 description 5
- ASPDJZINBYYZRU-UHFFFAOYSA-N 5-amino-2-chlorobenzotrifluoride Chemical compound NC1=CC=C(Cl)C(C(F)(F)F)=C1 ASPDJZINBYYZRU-UHFFFAOYSA-N 0.000 description 5
- 150000001408 amides Chemical class 0.000 description 5
- 239000002585 base Substances 0.000 description 5
- 230000015572 biosynthetic process Effects 0.000 description 5
- 239000003960 organic solvent Substances 0.000 description 5
- 229910052760 oxygen Inorganic materials 0.000 description 5
- 238000012360 testing method Methods 0.000 description 5
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 4
- XFCCEQWMNRJBBT-UHFFFAOYSA-N 2-(4-chlorophenyl)-n-[4-fluoro-3-(trifluoromethyl)phenyl]-4,5-dihydro-1,3-thiazole-4-carboxamide Chemical compound C1=C(C(F)(F)F)C(F)=CC=C1NC(=O)C1N=C(C=2C=CC(Cl)=CC=2)SC1 XFCCEQWMNRJBBT-UHFFFAOYSA-N 0.000 description 4
- QOSSAOTZNIDXMA-UHFFFAOYSA-N Dicylcohexylcarbodiimide Chemical compound C1CCCCC1N=C=NC1CCCCC1 QOSSAOTZNIDXMA-UHFFFAOYSA-N 0.000 description 4
- MCYHPZGUONZRGO-VKHMYHEASA-N L-cysteine methyl ester hydrochloride Natural products COC(=O)[C@@H](N)CS MCYHPZGUONZRGO-VKHMYHEASA-N 0.000 description 4
- WHOHXJZQBJXAKL-DFWYDOINSA-N Mecysteine hydrochloride Chemical compound Cl.COC(=O)[C@@H](N)CS WHOHXJZQBJXAKL-DFWYDOINSA-N 0.000 description 4
- 239000000556 agonist Substances 0.000 description 4
- 229940030486 androgens Drugs 0.000 description 4
- 239000000010 aprotic solvent Substances 0.000 description 4
- 238000009739 binding Methods 0.000 description 4
- 239000003054 catalyst Substances 0.000 description 4
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 4
- 125000005842 heteroatom Chemical group 0.000 description 4
- QYCCZOLZKAIDPM-UHFFFAOYSA-N methyl 2-(4-chlorophenyl)-4,5-dihydro-1,3-thiazole-4-carboxylate Chemical compound COC(=O)C1CSC(C=2C=CC(Cl)=CC=2)=N1 QYCCZOLZKAIDPM-UHFFFAOYSA-N 0.000 description 4
- MNNUSNWKRBLWIP-UHFFFAOYSA-N methyl 2-(4-fluorophenyl)-4,5-dihydro-1,3-thiazole-4-carboxylate Chemical compound COC(=O)C1CSC(C=2C=CC(F)=CC=2)=N1 MNNUSNWKRBLWIP-UHFFFAOYSA-N 0.000 description 4
- 229910052757 nitrogen Inorganic materials 0.000 description 4
- 125000006239 protecting group Chemical group 0.000 description 4
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 4
- 102000005962 receptors Human genes 0.000 description 4
- 108020003175 receptors Proteins 0.000 description 4
- 229910052717 sulfur Inorganic materials 0.000 description 4
- 229960003604 testosterone Drugs 0.000 description 4
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 description 4
- MAGCVRLGTQSVGF-UHFFFAOYSA-N 2-amino-2-methyl-3-sulfanylpropanoic acid;hydrochloride Chemical compound Cl.SCC(N)(C)C(O)=O MAGCVRLGTQSVGF-UHFFFAOYSA-N 0.000 description 3
- GNVFCXUZQGCXPB-UHFFFAOYSA-N 4-(trifluoromethylsulfonyl)aniline Chemical compound NC1=CC=C(S(=O)(=O)C(F)(F)F)C=C1 GNVFCXUZQGCXPB-UHFFFAOYSA-N 0.000 description 3
- PGFQDLOMDIBAPY-UHFFFAOYSA-N 4-fluoro-3-(trifluoromethyl)aniline Chemical compound NC1=CC=C(F)C(C(F)(F)F)=C1 PGFQDLOMDIBAPY-UHFFFAOYSA-N 0.000 description 3
- HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- 241001465754 Metazoa Species 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 230000027455 binding Effects 0.000 description 3
- 239000000872 buffer Substances 0.000 description 3
- 210000004027 cell Anatomy 0.000 description 3
- UAOMVDZJSHZZME-UHFFFAOYSA-N diisopropylamine Chemical compound CC(C)NC(C)C UAOMVDZJSHZZME-UHFFFAOYSA-N 0.000 description 3
- LTTYALGTCLODFB-UHFFFAOYSA-N ethyl 2-tert-butyl-3-formyl-4-methyl-1,3-thiazolidine-4-carboxylate Chemical compound CCOC(=O)C1(C)CSC(C(C)(C)C)N1C=O LTTYALGTCLODFB-UHFFFAOYSA-N 0.000 description 3
- WWVBRUOYKGDMFY-UHFFFAOYSA-N ethyl 3-chlorobenzenecarboximidate;hydrochloride Chemical compound Cl.CCOC(=N)C1=CC=CC(Cl)=C1 WWVBRUOYKGDMFY-UHFFFAOYSA-N 0.000 description 3
- LMVAXOJOCSZBFJ-UHFFFAOYSA-N ethyl 4-chlorobenzenecarboximidate;hydrochloride Chemical compound Cl.CCOC(=N)C1=CC=C(Cl)C=C1 LMVAXOJOCSZBFJ-UHFFFAOYSA-N 0.000 description 3
- LSHNGZSFDOJMSL-UHFFFAOYSA-N methyl 2-(3-fluorophenyl)-4,5-dihydro-1,3-thiazole-4-carboxylate Chemical compound COC(=O)C1CSC(C=2C=C(F)C=CC=2)=N1 LSHNGZSFDOJMSL-UHFFFAOYSA-N 0.000 description 3
- 150000004702 methyl esters Chemical class 0.000 description 3
- PFPIHUICWDCWSX-UHFFFAOYSA-N n-[4-cyano-3-(trifluoromethyl)phenyl]-2-(3-fluorophenyl)-4,5-dihydro-1,3-thiazole-4-carboxamide Chemical compound FC1=CC=CC(C=2SCC(N=2)C(=O)NC=2C=C(C(C#N)=CC=2)C(F)(F)F)=C1 PFPIHUICWDCWSX-UHFFFAOYSA-N 0.000 description 3
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- 150000003431 steroids Chemical class 0.000 description 3
- 238000003786 synthesis reaction Methods 0.000 description 3
- LMDZBCPBFSXMTL-UHFFFAOYSA-N 1-Ethyl-3-(3-dimethylaminopropyl)carbodiimide Substances CCN=C=NCCCN(C)C LMDZBCPBFSXMTL-UHFFFAOYSA-N 0.000 description 2
- NVKAWKQGWWIWPM-ABEVXSGRSA-N 17-β-hydroxy-5-α-Androstan-3-one Chemical compound C1C(=O)CC[C@]2(C)[C@H]3CC[C@](C)([C@H](CC4)O)[C@@H]4[C@@H]3CC[C@H]21 NVKAWKQGWWIWPM-ABEVXSGRSA-N 0.000 description 2
- ZNTIFRKAJRYQRO-UHFFFAOYSA-N 2-(3-chlorophenyl)-n-[2-fluoro-3-(trifluoromethyl)phenyl]-4,5-dihydro-1,3-thiazole-4-carboxamide Chemical compound C1=CC=C(C(F)(F)F)C(F)=C1NC(=O)C1N=C(C=2C=C(Cl)C=CC=2)SC1 ZNTIFRKAJRYQRO-UHFFFAOYSA-N 0.000 description 2
- QGNULCHCWROESD-UHFFFAOYSA-N 2-(3-chlorophenyl)-n-[4-(trifluoromethylsulfonyl)phenyl]-4,5-dihydro-1,3-thiazole-4-carboxamide Chemical compound C1=CC(S(=O)(=O)C(F)(F)F)=CC=C1NC(=O)C1N=C(C=2C=C(Cl)C=CC=2)SC1 QGNULCHCWROESD-UHFFFAOYSA-N 0.000 description 2
- WKUKOBWAASRADE-UHFFFAOYSA-N 2-(3-chlorophenyl)-n-[4-chloro-3-(trifluoromethyl)phenyl]-4,5-dihydro-1,3-thiazole-4-carboxamide Chemical compound C1=C(Cl)C(C(F)(F)F)=CC(NC(=O)C2N=C(SC2)C=2C=C(Cl)C=CC=2)=C1 WKUKOBWAASRADE-UHFFFAOYSA-N 0.000 description 2
- PIJNETUBDIGJPK-UHFFFAOYSA-N 2-(3-chlorophenyl)-n-[4-cyano-3-(trifluoromethyl)phenyl]-4,5-dihydro-1,3-thiazole-4-carboxamide Chemical compound C1=C(C#N)C(C(F)(F)F)=CC(NC(=O)C2N=C(SC2)C=2C=C(Cl)C=CC=2)=C1 PIJNETUBDIGJPK-UHFFFAOYSA-N 0.000 description 2
- YXOQSARWWNYIHA-UHFFFAOYSA-N 2-(3-chlorophenyl)-n-[4-nitro-3-(trifluoromethyl)phenyl]-4,5-dihydro-1,3-thiazole-4-carboxamide Chemical compound C1=C(C(F)(F)F)C([N+](=O)[O-])=CC=C1NC(=O)C1N=C(C=2C=C(Cl)C=CC=2)SC1 YXOQSARWWNYIHA-UHFFFAOYSA-N 0.000 description 2
- MWWZADAZLWHISD-UHFFFAOYSA-N 2-(3-fluorophenyl)-4,5-dihydro-1,3-thiazole-4-carboxylic acid Chemical compound OC(=O)C1CSC(C=2C=C(F)C=CC=2)=N1 MWWZADAZLWHISD-UHFFFAOYSA-N 0.000 description 2
- SLBROQBAMMOHOC-UHFFFAOYSA-N 2-(3-fluorophenyl)-n-[4-fluoro-3-(trifluoromethyl)phenyl]-4,5-dihydro-1,3-thiazole-4-carboxamide Chemical compound FC1=CC=CC(C=2SCC(N=2)C(=O)NC=2C=C(C(F)=CC=2)C(F)(F)F)=C1 SLBROQBAMMOHOC-UHFFFAOYSA-N 0.000 description 2
- KZWZEIHFIOUWHI-UHFFFAOYSA-N 2-(4-chlorophenyl)-n-(4-cyano-2,5-difluorophenyl)-5,5-dimethyl-4h-1,3-thiazole-4-carboxamide Chemical compound CC1(C)SC(C=2C=CC(Cl)=CC=2)=NC1C(=O)NC1=CC(F)=C(C#N)C=C1F KZWZEIHFIOUWHI-UHFFFAOYSA-N 0.000 description 2
- UHEVRJNCJNADFK-UHFFFAOYSA-N 2-(4-chlorophenyl)-n-[2-fluoro-3-(trifluoromethyl)phenyl]-4,5-dihydro-1,3-thiazole-4-carboxamide Chemical compound C1=CC=C(C(F)(F)F)C(F)=C1NC(=O)C1N=C(C=2C=CC(Cl)=CC=2)SC1 UHEVRJNCJNADFK-UHFFFAOYSA-N 0.000 description 2
- XSWPUSDYVOLIOI-UHFFFAOYSA-N 2-(4-chlorophenyl)-n-[4-(trifluoromethylsulfonyl)phenyl]-4,5-dihydro-1,3-thiazole-4-carboxamide Chemical compound C1=CC(S(=O)(=O)C(F)(F)F)=CC=C1NC(=O)C1N=C(C=2C=CC(Cl)=CC=2)SC1 XSWPUSDYVOLIOI-UHFFFAOYSA-N 0.000 description 2
- ZXKWUWJIMCLDIG-UHFFFAOYSA-N 2-(4-chlorophenyl)-n-[4-chloro-3-(trifluoromethyl)phenyl]-4,5-dihydro-1,3-thiazole-4-carboxamide Chemical compound C1=C(Cl)C(C(F)(F)F)=CC(NC(=O)C2N=C(SC2)C=2C=CC(Cl)=CC=2)=C1 ZXKWUWJIMCLDIG-UHFFFAOYSA-N 0.000 description 2
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- 238000004237 preparative chromatography Methods 0.000 description 1
- 230000035755 proliferation Effects 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 210000002307 prostate Anatomy 0.000 description 1
- 238000000159 protein binding assay Methods 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 125000001042 pteridinyl group Chemical group N1=C(N=CC2=NC=CN=C12)* 0.000 description 1
- 125000000561 purinyl group Chemical group N1=C(N=C2N=CNC2=C1)* 0.000 description 1
- 125000004309 pyranyl group Chemical group O1C(C=CC=C1)* 0.000 description 1
- 125000003373 pyrazinyl group Chemical group 0.000 description 1
- 125000002098 pyridazinyl group Chemical group 0.000 description 1
- 125000004076 pyridyl group Chemical group 0.000 description 1
- 125000000714 pyrimidinyl group Chemical group 0.000 description 1
- 125000000168 pyrrolyl group Chemical group 0.000 description 1
- 125000002294 quinazolinyl group Chemical group N1=C(N=CC2=CC=CC=C12)* 0.000 description 1
- 125000002943 quinolinyl group Chemical group N1=C(C=CC2=CC=CC=C12)* 0.000 description 1
- 230000008929 regeneration Effects 0.000 description 1
- 238000011069 regeneration method Methods 0.000 description 1
- 210000004994 reproductive system Anatomy 0.000 description 1
- 239000012465 retentate Substances 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 210000002966 serum Anatomy 0.000 description 1
- 230000001568 sexual effect Effects 0.000 description 1
- 150000003384 small molecules Chemical class 0.000 description 1
- 239000011684 sodium molybdate Substances 0.000 description 1
- 235000015393 sodium molybdate Nutrition 0.000 description 1
- TVXXNOYZHKPKGW-UHFFFAOYSA-N sodium molybdate (anhydrous) Chemical compound [Na+].[Na+].[O-][Mo]([O-])(=O)=O TVXXNOYZHKPKGW-UHFFFAOYSA-N 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 239000003270 steroid hormone Substances 0.000 description 1
- 230000003637 steroidlike Effects 0.000 description 1
- 208000024891 symptom Diseases 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 210000001550 testis Anatomy 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 238000002560 therapeutic procedure Methods 0.000 description 1
- 125000001113 thiadiazolyl group Chemical group 0.000 description 1
- 125000002769 thiazolinyl group Chemical group 0.000 description 1
- 125000001544 thienyl group Chemical group 0.000 description 1
- 125000001425 triazolyl group Chemical group 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
- C07D277/08—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
- C07D277/12—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/14—Prodigestives, e.g. acids, enzymes, appetite stimulants, antidyspeptics, tonics, antiflatulents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/08—Drugs for disorders of the urinary system of the prostate
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
- A61P15/08—Drugs for genital or sexual disorders; Contraceptives for gonadal disorders or for enhancing fertility, e.g. inducers of ovulation or of spermatogenesis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/14—Drugs for dermatological disorders for baldness or alopecia
-
- 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
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
- A61P31/18—Antivirals for RNA viruses for HIV
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P5/00—Drugs for disorders of the endocrine system
- A61P5/24—Drugs for disorders of the endocrine system of the sex hormones
- A61P5/26—Androgens
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Virology (AREA)
- Dermatology (AREA)
- Endocrinology (AREA)
- Reproductive Health (AREA)
- AIDS & HIV (AREA)
- Molecular Biology (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Gynecology & Obstetrics (AREA)
- Pregnancy & Childbirth (AREA)
- Tropical Medicine & Parasitology (AREA)
- Diabetes (AREA)
- Urology & Nephrology (AREA)
- Nutrition Science (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Thiazole And Isothizaole Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US47871203P | 2003-06-13 | 2003-06-13 | |
| US478712P | 2003-06-13 | ||
| PCT/US2004/018665 WO2004113309A1 (en) | 2003-06-13 | 2004-06-12 | Thiazoline derivatives as selective androgen receptor modulators (sarms) |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| DE602004008300D1 DE602004008300D1 (de) | 2007-09-27 |
| DE602004008300T2 true DE602004008300T2 (de) | 2008-05-08 |
Family
ID=33539114
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE602004008300T Expired - Lifetime DE602004008300T2 (de) | 2003-06-13 | 2004-06-12 | Thiazolinderivate als selektive androgenrezeptormodulatoren (sarms) |
Country Status (14)
| Country | Link |
|---|---|
| US (1) | US20050014952A1 (enExample) |
| EP (1) | EP1656360B1 (enExample) |
| JP (1) | JP4898446B2 (enExample) |
| CN (1) | CN1835937B (enExample) |
| AT (1) | ATE370133T1 (enExample) |
| AU (1) | AU2004249697B2 (enExample) |
| CA (1) | CA2528764A1 (enExample) |
| CY (1) | CY1106973T1 (enExample) |
| DE (1) | DE602004008300T2 (enExample) |
| DK (1) | DK1656360T3 (enExample) |
| ES (1) | ES2291906T3 (enExample) |
| PL (1) | PL1656360T3 (enExample) |
| PT (1) | PT1656360E (enExample) |
| WO (1) | WO2004113309A1 (enExample) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101103003A (zh) | 2004-11-16 | 2008-01-09 | 詹森药业有限公司 | 用作选择性雄激素受体调节剂(sarms)的新的杂环衍生物 |
| US7709516B2 (en) | 2005-06-17 | 2010-05-04 | Endorecherche, Inc. | Helix 12 directed non-steroidal antiandrogens |
| US9284345B2 (en) | 2007-04-12 | 2016-03-15 | Endorecherche, Inc. | 17alpha-substituted steroids as systemic antiandrogens and selective androgen receptor modulators |
| EP3608317A1 (en) * | 2012-01-12 | 2020-02-12 | Yale University | Compounds & methods for the enhanced degradation of targeted proteins & other polypeptides by an e3 ubiquitin ligase |
| CN103450112B (zh) * | 2013-08-07 | 2019-09-13 | 华东理工大学 | 一种n-桥连接的含氮五元杂环化合物及其制备与用途 |
| US9682960B2 (en) | 2013-12-19 | 2017-06-20 | Endorecherche, Inc. | Non-steroidal antiandrogens and selective androgen receptor modulators with a pyridyl moiety |
| EA202092436A1 (ru) | 2018-05-14 | 2021-05-04 | Нувейшн Био Инк. | Противораковые соединения, нацеливающие на ядерные гормональные рецепторы |
| CA3138197A1 (en) | 2019-05-14 | 2020-11-19 | Nuvation Bio Inc. | Anti-cancer nuclear hormone receptor-targeting compounds |
| US11952349B2 (en) | 2019-11-13 | 2024-04-09 | Nuvation Bio Inc. | Anti-cancer nuclear hormone receptor-targeting compounds |
| IL306010A (en) | 2021-03-23 | 2023-11-01 | Nuvation Bio Inc | Anticancer compounds against the nuclear hormone receptor |
| JP2024516024A (ja) | 2021-05-03 | 2024-04-11 | ニューベイション・バイオ・インコーポレイテッド | 抗がん核内ホルモン受容体標的化化合物 |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1143957A (zh) * | 1994-01-24 | 1997-02-26 | 纳幕尔杜邦公司 | 杀节肢动物的2-噁唑啉和2-噻唑啉 |
| US6403623B1 (en) * | 1999-05-27 | 2002-06-11 | Unuversity Of Notre Dame Du Lac | Heterocyclic antituberculosis agents |
| ES2321933T3 (es) * | 2000-08-24 | 2009-06-15 | University Of Tennessee Research Foundation | Moduladores selectivos del receptor de androgeno y metodos de uso de los mismos. |
-
2004
- 2004-06-12 ES ES04755044T patent/ES2291906T3/es not_active Expired - Lifetime
- 2004-06-12 CN CN2004800230915A patent/CN1835937B/zh not_active Expired - Fee Related
- 2004-06-12 DK DK04755044T patent/DK1656360T3/da active
- 2004-06-12 AT AT04755044T patent/ATE370133T1/de active
- 2004-06-12 DE DE602004008300T patent/DE602004008300T2/de not_active Expired - Lifetime
- 2004-06-12 WO PCT/US2004/018665 patent/WO2004113309A1/en not_active Ceased
- 2004-06-12 US US10/866,591 patent/US20050014952A1/en not_active Abandoned
- 2004-06-12 AU AU2004249697A patent/AU2004249697B2/en not_active Ceased
- 2004-06-12 JP JP2006533745A patent/JP4898446B2/ja not_active Expired - Fee Related
- 2004-06-12 EP EP04755044A patent/EP1656360B1/en not_active Expired - Lifetime
- 2004-06-12 PT PT04755044T patent/PT1656360E/pt unknown
- 2004-06-12 PL PL04755044T patent/PL1656360T3/pl unknown
- 2004-06-12 CA CA002528764A patent/CA2528764A1/en not_active Abandoned
-
2007
- 2007-11-05 CY CY20071101413T patent/CY1106973T1/el unknown
Also Published As
| Publication number | Publication date |
|---|---|
| AU2004249697A1 (en) | 2004-12-29 |
| AU2004249697B2 (en) | 2010-04-22 |
| JP4898446B2 (ja) | 2012-03-14 |
| WO2004113309A1 (en) | 2004-12-29 |
| CA2528764A1 (en) | 2004-12-29 |
| US20050014952A1 (en) | 2005-01-20 |
| EP1656360A1 (en) | 2006-05-17 |
| DE602004008300D1 (de) | 2007-09-27 |
| ES2291906T3 (es) | 2008-03-01 |
| CN1835937A (zh) | 2006-09-20 |
| CN1835937B (zh) | 2012-07-18 |
| PL1656360T3 (pl) | 2008-01-31 |
| PT1656360E (pt) | 2007-10-22 |
| EP1656360B1 (en) | 2007-08-15 |
| CY1106973T1 (el) | 2012-09-26 |
| DK1656360T3 (da) | 2007-12-27 |
| JP2007501287A (ja) | 2007-01-25 |
| ATE370133T1 (de) | 2007-09-15 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| 8381 | Inventor (new situation) |
Inventor name: NG, RAYMOND A., RARITAN, NJ 08869-0602, US Inventor name: SUI, ZHIHUA, RARITAN, NJ 08869-0602, US |
|
| 8364 | No opposition during term of opposition |