TWI303636B - Pyrazole compositions useful as protein kinase inhibitors - Google Patents
Pyrazole compositions useful as protein kinase inhibitors Download PDFInfo
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- TWI303636B TWI303636B TW090122889A TW90122889A TWI303636B TW I303636 B TWI303636 B TW I303636B TW 090122889 A TW090122889 A TW 090122889A TW 90122889 A TW90122889 A TW 90122889A TW I303636 B TWI303636 B TW I303636B
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- group
- ring
- aliphatic group
- alkyl
- aliphatic
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- 239000000203 mixture Substances 0.000 title description 106
- WTKZEGDFNFYCGP-UHFFFAOYSA-N Pyrazole Chemical compound C=1C=NNC=1 WTKZEGDFNFYCGP-UHFFFAOYSA-N 0.000 title description 8
- 239000003909 protein kinase inhibitor Substances 0.000 title description 7
- 229940045988 antineoplastic drug protein kinase inhibitors Drugs 0.000 title description 4
- 125000001931 aliphatic group Chemical group 0.000 claims description 505
- -1 hexahydropyridyl Chemical group 0.000 claims description 285
- 150000001875 compounds Chemical class 0.000 claims description 258
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical group N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 241
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 209
- 125000000217 alkyl group Chemical group 0.000 claims description 198
- 125000001424 substituent group Chemical group 0.000 claims description 192
- 229910052757 nitrogen Chemical group 0.000 claims description 168
- 229910052739 hydrogen Inorganic materials 0.000 claims description 147
- 239000001257 hydrogen Substances 0.000 claims description 145
- 125000004429 atom Chemical group 0.000 claims description 125
- OAKJQQAXSVQMHS-UHFFFAOYSA-N hydrazine Substances NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 claims description 98
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 85
- 201000010099 disease Diseases 0.000 claims description 84
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 83
- 125000005843 halogen group Chemical group 0.000 claims description 81
- 125000004076 pyridyl group Chemical group 0.000 claims description 79
- 229910052799 carbon Inorganic materials 0.000 claims description 60
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 59
- 125000004122 cyclic group Chemical group 0.000 claims description 54
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 52
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 52
- 239000003112 inhibitor Substances 0.000 claims description 51
- 125000003983 fluorenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3CC12)* 0.000 claims description 50
- 125000005842 heteroatom Chemical group 0.000 claims description 50
- 102000001267 GSK3 Human genes 0.000 claims description 49
- 108010014905 Glycogen Synthase Kinase 3 Proteins 0.000 claims description 49
- 230000000694 effects Effects 0.000 claims description 49
- 150000002431 hydrogen Chemical group 0.000 claims description 47
- 229910052760 oxygen Inorganic materials 0.000 claims description 46
- 239000001301 oxygen Substances 0.000 claims description 46
- 230000002401 inhibitory effect Effects 0.000 claims description 45
- 229910052717 sulfur Inorganic materials 0.000 claims description 45
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 44
- 239000011593 sulfur Chemical group 0.000 claims description 40
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 39
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 39
- 239000005441 aurora Substances 0.000 claims description 38
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims description 38
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 37
- 239000008194 pharmaceutical composition Substances 0.000 claims description 36
- 206010028980 Neoplasm Diseases 0.000 claims description 35
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 34
- 125000004008 6 membered carbocyclic group Chemical group 0.000 claims description 32
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 32
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 31
- 125000001475 halogen functional group Chemical group 0.000 claims description 30
- 201000011510 cancer Diseases 0.000 claims description 27
- 238000009830 intercalation Methods 0.000 claims description 26
- 125000000714 pyrimidinyl group Chemical group 0.000 claims description 26
- 125000002837 carbocyclic group Chemical group 0.000 claims description 24
- 239000000460 chlorine Substances 0.000 claims description 24
- 239000012472 biological sample Substances 0.000 claims description 23
- 101150090422 gsk-3 gene Proteins 0.000 claims description 23
- 230000015572 biosynthetic process Effects 0.000 claims description 22
- 125000002757 morpholinyl group Chemical group 0.000 claims description 22
- 208000024827 Alzheimer disease Diseases 0.000 claims description 21
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 21
- 239000002244 precipitate Substances 0.000 claims description 20
- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 claims description 19
- 125000003226 pyrazolyl group Chemical group 0.000 claims description 19
- 238000003786 synthesis reaction Methods 0.000 claims description 18
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical group C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims description 17
- 125000005577 anthracene group Chemical group 0.000 claims description 17
- 206010012601 diabetes mellitus Diseases 0.000 claims description 16
- 239000003814 drug Substances 0.000 claims description 16
- 125000000904 isoindolyl group Chemical group C=1(NC=C2C=CC=CC12)* 0.000 claims description 16
- 238000002360 preparation method Methods 0.000 claims description 16
- 125000002943 quinolinyl group Chemical group N1=C(C=CC2=CC=CC=C12)* 0.000 claims description 15
- 125000003396 thiol group Chemical group [H]S* 0.000 claims description 15
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 14
- 241001122767 Theaceae Species 0.000 claims description 14
- 239000007789 gas Substances 0.000 claims description 14
- 125000001624 naphthyl group Chemical group 0.000 claims description 14
- 229920002527 Glycogen Polymers 0.000 claims description 13
- 125000005605 benzo group Chemical group 0.000 claims description 13
- 125000006165 cyclic alkyl group Chemical group 0.000 claims description 13
- 229940096919 glycogen Drugs 0.000 claims description 13
- 229910052736 halogen Inorganic materials 0.000 claims description 13
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 claims description 12
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 12
- 108090000623 proteins and genes Proteins 0.000 claims description 12
- 125000001544 thienyl group Chemical group 0.000 claims description 12
- 210000004369 blood Anatomy 0.000 claims description 11
- 239000008280 blood Substances 0.000 claims description 11
- 229910052731 fluorine Inorganic materials 0.000 claims description 11
- 239000008103 glucose Substances 0.000 claims description 11
- 125000002883 imidazolyl group Chemical group 0.000 claims description 11
- 201000000980 schizophrenia Diseases 0.000 claims description 11
- 239000003937 drug carrier Substances 0.000 claims description 10
- 238000004519 manufacturing process Methods 0.000 claims description 10
- 102000004169 proteins and genes Human genes 0.000 claims description 10
- 229910052801 chlorine Inorganic materials 0.000 claims description 9
- KJTLSVCANCCWHF-UHFFFAOYSA-N Ruthenium Chemical compound [Ru] KJTLSVCANCCWHF-UHFFFAOYSA-N 0.000 claims description 8
- 150000002367 halogens Chemical class 0.000 claims description 8
- 150000002632 lipids Chemical class 0.000 claims description 8
- 125000000168 pyrrolyl group Chemical group 0.000 claims description 8
- 238000006467 substitution reaction Methods 0.000 claims description 8
- 125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 7
- 238000003780 insertion Methods 0.000 claims description 7
- 230000037431 insertion Effects 0.000 claims description 7
- 229940124597 therapeutic agent Drugs 0.000 claims description 7
- 125000000339 4-pyridyl group Chemical group N1=C([H])C([H])=C([*])C([H])=C1[H] 0.000 claims description 6
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 claims description 6
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims description 6
- 230000002708 enhancing effect Effects 0.000 claims description 6
- 125000002541 furyl group Chemical group 0.000 claims description 6
- 125000001188 haloalkyl group Chemical group 0.000 claims description 6
- 150000002829 nitrogen Chemical class 0.000 claims description 6
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 claims description 6
- 125000004105 2-pyridyl group Chemical group N1=C([*])C([H])=C([H])C([H])=C1[H] 0.000 claims description 5
- 150000001721 carbon Chemical class 0.000 claims description 5
- 229910052707 ruthenium Inorganic materials 0.000 claims description 5
- 229910021653 sulphate ion Inorganic materials 0.000 claims description 5
- YLQBMQCUIZJEEH-UHFFFAOYSA-N Furan Chemical compound C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 claims description 4
- 125000000609 carbazolyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3NC12)* 0.000 claims description 4
- 230000026731 phosphorylation Effects 0.000 claims description 4
- 238000006366 phosphorylation reaction Methods 0.000 claims description 4
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Chemical group COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims description 4
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 3
- MDFFNEOEWAXZRQ-UHFFFAOYSA-N aminyl Chemical compound [NH2] MDFFNEOEWAXZRQ-UHFFFAOYSA-N 0.000 claims description 3
- 229910052786 argon Inorganic materials 0.000 claims description 3
- 125000000524 functional group Chemical group 0.000 claims description 3
- 125000005740 oxycarbonyl group Chemical group [*:1]OC([*:2])=O 0.000 claims description 3
- 239000004576 sand Substances 0.000 claims description 3
- 108060006662 GSK3 Proteins 0.000 claims description 2
- NFVJNJQRWPQVOA-UHFFFAOYSA-N n-[2-chloro-5-(trifluoromethyl)phenyl]-2-[3-(4-ethyl-5-ethylsulfanyl-1,2,4-triazol-3-yl)piperidin-1-yl]acetamide Chemical compound CCN1C(SCC)=NN=C1C1CN(CC(=O)NC=2C(=CC=C(C=2)C(F)(F)F)Cl)CCC1 NFVJNJQRWPQVOA-UHFFFAOYSA-N 0.000 claims description 2
- 125000001584 benzyloxycarbonyl group Chemical group C(=O)(OCC1=CC=CC=C1)* 0.000 claims 8
- UYWQUFXKFGHYNT-UHFFFAOYSA-N phenylmethyl ester of formic acid Natural products O=COCC1=CC=CC=C1 UYWQUFXKFGHYNT-UHFFFAOYSA-N 0.000 claims 5
- 125000006367 bivalent amino carbonyl group Chemical group [H]N([*:1])C([*:2])=O 0.000 claims 3
- 125000000565 sulfonamide group Chemical group 0.000 claims 3
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 claims 2
- 102000002254 Glycogen Synthase Kinase 3 Human genes 0.000 claims 2
- OQJVXNHMUWQQEW-UHFFFAOYSA-N 1,2,3,4-tetrahydropyrazine Chemical group C1CNC=CN1 OQJVXNHMUWQQEW-UHFFFAOYSA-N 0.000 claims 1
- UKZJZMLGGSGZMI-UHFFFAOYSA-N 2,3,4,7,8,9-hexahydro-1h-purine Chemical compound N1CNC=C2NCNC21 UKZJZMLGGSGZMI-UHFFFAOYSA-N 0.000 claims 1
- 241001478240 Coccus Species 0.000 claims 1
- 229940126062 Compound A Drugs 0.000 claims 1
- 241000196324 Embryophyta Species 0.000 claims 1
- NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 claims 1
- 150000001555 benzenes Chemical class 0.000 claims 1
- RQIDGZHMTWSMMC-TZNPKLQUSA-N juvenile hormone I Chemical compound COC(=O)/C=C(C)/CC\C=C(/CC)CC[C@H]1O[C@@]1(C)CC RQIDGZHMTWSMMC-TZNPKLQUSA-N 0.000 claims 1
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 claims 1
- 210000004508 polar body Anatomy 0.000 claims 1
- 125000001725 pyrenyl group Chemical group 0.000 claims 1
- LISFMEBWQUVKPJ-UHFFFAOYSA-N quinolin-2-ol Chemical compound C1=CC=C2NC(=O)C=CC2=C1 LISFMEBWQUVKPJ-UHFFFAOYSA-N 0.000 claims 1
- 229910052703 rhodium Inorganic materials 0.000 claims 1
- 239000010948 rhodium Substances 0.000 claims 1
- MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 claims 1
- 125000002345 steroid group Chemical group 0.000 claims 1
- 238000000034 method Methods 0.000 description 271
- 125000004093 cyano group Chemical group *C#N 0.000 description 149
- 125000001072 heteroaryl group Chemical group 0.000 description 133
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- 125000000623 heterocyclic group Chemical group 0.000 description 90
- IAZDPXIOMUYVGZ-WFGJKAKNSA-N Dimethyl sulfoxide Chemical compound [2H]C([2H])([2H])S(=O)C([2H])([2H])[2H] IAZDPXIOMUYVGZ-WFGJKAKNSA-N 0.000 description 85
- 125000000468 ketone group Chemical group 0.000 description 61
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 45
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- 125000006413 ring segment Chemical group 0.000 description 36
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- 125000006569 (C5-C6) heterocyclic group Chemical group 0.000 description 30
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| US6184226B1 (en) * | 1998-08-28 | 2001-02-06 | Scios Inc. | Quinazoline derivatives as inhibitors of P-38 α |
| US6982260B1 (en) | 1999-11-22 | 2006-01-03 | Warner-Lambert Company | Quinazolines and their use for inhibiting cyclin-dependent kinase enzymes |
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Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TWI476192B (zh) * | 2009-02-27 | 2015-03-11 | Ambit Biosciences Corp | Jak激酶調節化合物及其使用方法 |
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