JP2004502763A5

JP2004502763A5 -

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Publication number: JP2004502763A5
Authority: JP; Japan
Prior art keywords: sulfamoyl; alkyl; formula; compound; mmol
Prior art date: 2001-07-06
Legal status : Pending

Application number

JP2002509296A

Other languages

English (en)

Japanese (ja)

Other versions

JP2004502763A (ja

Filing date

2001-07-06

Publication date

2008-08-28

2000-07-11 Priority claimed from GBGB0016877.3A external-priority patent/GB0016877D0/en

2001-07-06 Application filed filed Critical

2004-01-29 Publication of JP2004502763A publication Critical patent/JP2004502763A/ja

2008-08-28 Publication of JP2004502763A5 publication Critical patent/JP2004502763A5/ja

Status Pending legal-status Critical Current

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-1 nitro, cyano, hydroxy, amino, carboxy, carbamoyl Chemical group 0.000 description 419
150000001875 compounds Chemical class 0.000 description 193
238000000034 method Methods 0.000 description 162
229910052757 nitrogen Inorganic materials 0.000 description 96
IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 82
125000000623 heterocyclic group Chemical group 0.000 description 72
150000003839 salts Chemical class 0.000 description 66
150000002148 esters Chemical class 0.000 description 60
238000001727 in vivo Methods 0.000 description 57
229910052799 carbon Inorganic materials 0.000 description 49
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 48
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 47
125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 description 44
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 38
125000000882 C2-C6 alkenyl group Chemical group 0.000 description 37
239000003814 drug Substances 0.000 description 35
125000003601 C2-C6 alkynyl group Chemical group 0.000 description 31
241001465754 Metazoa Species 0.000 description 30
239000000203 mixture Substances 0.000 description 30
206010028980 Neoplasm Diseases 0.000 description 29
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 28
210000004027 cell Anatomy 0.000 description 28
238000005481 NMR spectroscopy Methods 0.000 description 27
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 27
BTANRVKWQNVYAZ-UHFFFAOYSA-N butan-2-ol Chemical compound CCC(C)O BTANRVKWQNVYAZ-UHFFFAOYSA-N 0.000 description 27
230000002401 inhibitory effect Effects 0.000 description 27
QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 27
239000000243 solution Substances 0.000 description 27
PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 26
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 26
125000000217 alkyl group Chemical group 0.000 description 26
125000005843 halogen group Chemical group 0.000 description 26
229910052739 hydrogen Inorganic materials 0.000 description 26
239000001257 hydrogen Substances 0.000 description 26
238000006243 chemical reaction Methods 0.000 description 24
239000007787 solid Substances 0.000 description 21
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 20
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 20
238000001914 filtration Methods 0.000 description 20
FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 description 20
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 20
201000011510 cancer Diseases 0.000 description 19
125000002887 hydroxy group Chemical group [H]O* 0.000 description 19
239000007858 starting material Substances 0.000 description 19
108091007914 CDKs Proteins 0.000 description 18
108010024986 Cyclin-Dependent Kinase 2 Proteins 0.000 description 18
102100036239 Cyclin-dependent kinase 2 Human genes 0.000 description 18
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 18
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 18
125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 description 18
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 17
YMWUJEATGCHHMB-UHFFFAOYSA-N dichloromethane Natural products ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 17
230000000694 effects Effects 0.000 description 17
238000011282 treatment Methods 0.000 description 17
125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 description 16
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 16
CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 description 16
230000022131 cell cycle Effects 0.000 description 16
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 16
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 16
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 15
208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 15
238000001704 evaporation Methods 0.000 description 15
230000008020 evaporation Effects 0.000 description 15
230000035755 proliferation Effects 0.000 description 15
150000001412 amines Chemical class 0.000 description 13
235000019439 ethyl acetate Nutrition 0.000 description 13
238000004519 manufacturing process Methods 0.000 description 13
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 13
125000006239 protecting group Chemical group 0.000 description 13
KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 12
125000000753 cycloalkyl group Chemical group 0.000 description 12
208000035475 disorder Diseases 0.000 description 12
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 12
239000002904 solvent Substances 0.000 description 12
229910052717 sulfur Inorganic materials 0.000 description 12
125000002252 acyl group Chemical group 0.000 description 11
238000004587 chromatography analysis Methods 0.000 description 11
125000001153 fluoro group Chemical group F* 0.000 description 11
239000003112 inhibitor Substances 0.000 description 11
201000001320 Atherosclerosis Diseases 0.000 description 10
125000004453 alkoxycarbonyl group Chemical group 0.000 description 10
239000003085 diluting agent Substances 0.000 description 10
125000006125 ethylsulfonyl group Chemical group 0.000 description 10
230000003211 malignant effect Effects 0.000 description 10
125000004170 methylsulfonyl group Chemical group [H]C([H])([H])S(*)(=O)=O 0.000 description 10
239000008194 pharmaceutical composition Substances 0.000 description 10
YBYRMVIVWMBXKQ-UHFFFAOYSA-N phenylmethanesulfonyl fluoride Chemical compound FS(=O)(=O)CC1=CC=CC=C1 YBYRMVIVWMBXKQ-UHFFFAOYSA-N 0.000 description 10
125000004454 (C1-C6) alkoxycarbonyl group Chemical group 0.000 description 9
102000003909 Cyclin E Human genes 0.000 description 9
108090000257 Cyclin E Proteins 0.000 description 9
IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 9
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 9
125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 description 9
125000003754 ethoxycarbonyl group Chemical group C(=O)(OCC)* 0.000 description 9
208000032839 leukemia Diseases 0.000 description 9
125000001424 substituent group Chemical group 0.000 description 9
125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 8
SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 8
239000000872 buffer Substances 0.000 description 8
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 8
229910052760 oxygen Inorganic materials 0.000 description 8
150000003230 pyrimidines Chemical class 0.000 description 8
229920006395 saturated elastomer Polymers 0.000 description 8
201000004384 Alopecia Diseases 0.000 description 7
206010051113 Arterial restenosis Diseases 0.000 description 7
208000023275 Autoimmune disease Diseases 0.000 description 7
208000020084 Bone disease Diseases 0.000 description 7
108010025464 Cyclin-Dependent Kinase 4 Proteins 0.000 description 7
108010025468 Cyclin-Dependent Kinase 6 Proteins 0.000 description 7
102100036252 Cyclin-dependent kinase 4 Human genes 0.000 description 7
102100026804 Cyclin-dependent kinase 6 Human genes 0.000 description 7
208000007766 Kaposi sarcoma Diseases 0.000 description 7
208000022873 Ocular disease Diseases 0.000 description 7
201000004681 Psoriasis Diseases 0.000 description 7
230000001154 acute effect Effects 0.000 description 7
208000038016 acute inflammation Diseases 0.000 description 7
230000006022 acute inflammation Effects 0.000 description 7
125000004429 atom Chemical group 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
239000003054 catalyst Substances 0.000 description 7
208000037976 chronic inflammation Diseases 0.000 description 7
230000006020 chronic inflammation Effects 0.000 description 7
230000000893 fibroproliferative effect Effects 0.000 description 7
239000000706 filtrate Substances 0.000 description 7
230000003676 hair loss Effects 0.000 description 7
208000024963 hair loss Diseases 0.000 description 7
201000011066 hemangioma Diseases 0.000 description 7
230000005764 inhibitory process Effects 0.000 description 7
125000004573 morpholin-4-yl group Chemical group N1(CCOCC1)* 0.000 description 7
239000003921 oil Substances 0.000 description 7
230000002062 proliferating effect Effects 0.000 description 7
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 7
108090000623 proteins and genes Proteins 0.000 description 7
102000004169 proteins and genes Human genes 0.000 description 7
230000002207 retinal effect Effects 0.000 description 7
206010039073 rheumatoid arthritis Diseases 0.000 description 7
239000000377 silicon dioxide Substances 0.000 description 7
238000010561 standard procedure Methods 0.000 description 7
125000004434 sulfur atom Chemical group 0.000 description 7
125000004769 (C1-C4) alkylsulfonyl group Chemical group 0.000 description 6
IOOMXAQUNPWDLL-UHFFFAOYSA-N 2-[6-(diethylamino)-3-(diethyliminiumyl)-3h-xanthen-9-yl]-5-sulfobenzene-1-sulfonate Chemical compound C=12C=CC(=[N+](CC)CC)C=C2OC2=CC(N(CC)CC)=CC=C2C=1C1=CC=C(S(O)(=O)=O)C=C1S([O-])(=O)=O IOOMXAQUNPWDLL-UHFFFAOYSA-N 0.000 description 6
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 6
229960000583 acetic acid Drugs 0.000 description 6
239000002253 acid Substances 0.000 description 6
125000003277 amino group Chemical group 0.000 description 6
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 6
239000002585 base Substances 0.000 description 6
239000012267 brine Substances 0.000 description 6
KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 6
125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 description 6
239000002552 dosage form Substances 0.000 description 6
150000002431 hydrogen Chemical class 0.000 description 6
230000007062 hydrolysis Effects 0.000 description 6
238000006460 hydrolysis reaction Methods 0.000 description 6
125000002950 monocyclic group Chemical group 0.000 description 6
125000004433 nitrogen atom Chemical group N* 0.000 description 6
239000001301 oxygen Substances 0.000 description 6
125000004194 piperazin-1-yl group Chemical group [H]N1C([H])([H])C([H])([H])N(*)C([H])([H])C1([H])[H] 0.000 description 6
210000002307 prostate Anatomy 0.000 description 6
238000010992 reflux Methods 0.000 description 6
HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 6
239000011593 sulfur Substances 0.000 description 6
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 6
JKMHFZQWWAIEOD-UHFFFAOYSA-N 2-[4-(2-hydroxyethyl)piperazin-1-yl]ethanesulfonic acid Chemical compound OCC[NH+]1CCN(CCS([O-])(=O)=O)CC1 JKMHFZQWWAIEOD-UHFFFAOYSA-N 0.000 description 5
QAVCQCQQTYJKSO-UHFFFAOYSA-N 2-chloro-11-cyclopropyl-4-methyl-5h-dipyrido[2,3-b:2',3'-f][1,4]diazepin-6-one Chemical compound C12=NC=CC=C2C(=O)NC=2C(C)=CC(Cl)=NC=2N1C1CC1 QAVCQCQQTYJKSO-UHFFFAOYSA-N 0.000 description 5
125000001494 2-propynyl group Chemical group [H]C#CC([H])([H])* 0.000 description 5
VHYFNPMBLIVWCW-UHFFFAOYSA-N 4-Dimethylaminopyridine Chemical compound CN(C)C1=CC=NC=C1 VHYFNPMBLIVWCW-UHFFFAOYSA-N 0.000 description 5
102000016736 Cyclin Human genes 0.000 description 5
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125000002490 anilino group Chemical group [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 5
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AFABGHUZZDYHJO-UHFFFAOYSA-N 2-Methylpentane Chemical compound CCCC(C)C AFABGHUZZDYHJO-UHFFFAOYSA-N 0.000 description 4
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AOJJSUZBOXZQNB-TZSSRYMLSA-N Doxorubicin Chemical compound O([C@H]1C[C@@](O)(CC=2C(O)=C3C(=O)C=4C=CC=C(C=4C(=O)C3=C(O)C=21)OC)C(=O)CO)[C@H]1C[C@H](N)[C@H](O)[C@H](C)O1 AOJJSUZBOXZQNB-TZSSRYMLSA-N 0.000 description 4
239000007995 HEPES buffer Substances 0.000 description 4
OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 4
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RJURFGZVJUQBHK-UHFFFAOYSA-N actinomycin D Natural products CC1OC(=O)C(C(C)C)N(C)C(=O)CN(C)C(=O)C2CCCN2C(=O)C(C(C)C)NC(=O)C1NC(=O)C1=C(N)C(=O)C(C)=C2OC(C(C)=CC=C3C(=O)NC4C(=O)NC(C(N5CCCC5C(=O)N(C)CC(=O)N(C)C(C(C)C)C(=O)OC4C)=O)C(C)C)=C3N=C21 RJURFGZVJUQBHK-UHFFFAOYSA-N 0.000 description 4
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CBHOOMGKXCMKIR-UHFFFAOYSA-N azane;methanol Chemical compound N.OC CBHOOMGKXCMKIR-UHFFFAOYSA-N 0.000 description 4
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RCCPEORTSYDPMB-UHFFFAOYSA-N hydroxy benzenecarboximidothioate Chemical compound OSC(=N)C1=CC=CC=C1 RCCPEORTSYDPMB-UHFFFAOYSA-N 0.000 description 4
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BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 4
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JP2002509296A 2000-07-11 2001-07-06 ピリミジン誘導体 Pending JP2004502763A (ja)