CA2874911C - New compounds - Google Patents
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- Publication number
- CA2874911C CA2874911C CA2874911A CA2874911A CA2874911C CA 2874911 C CA2874911 C CA 2874911C CA 2874911 A CA2874911 A CA 2874911A CA 2874911 A CA2874911 A CA 2874911A CA 2874911 C CA2874911 C CA 2874911C
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- CA
- Canada
- Prior art keywords
- substituted
- 6alkyl
- cancer
- salkyl
- compound
- Prior art date
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- 150000001875 compounds Chemical class 0.000 title claims abstract description 413
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- 238000011282 treatment Methods 0.000 claims abstract description 116
- -1 naphthyridine derivative compounds Chemical class 0.000 claims abstract description 77
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- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims abstract description 65
- 201000010099 disease Diseases 0.000 claims abstract description 60
- 239000008194 pharmaceutical composition Substances 0.000 claims abstract description 16
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 113
- 108091008794 FGF receptors Proteins 0.000 claims description 84
- 229910052739 hydrogen Inorganic materials 0.000 claims description 77
- 239000001257 hydrogen Substances 0.000 claims description 77
- 125000005842 heteroatom Chemical group 0.000 claims description 59
- 150000003839 salts Chemical class 0.000 claims description 51
- 229910052736 halogen Inorganic materials 0.000 claims description 48
- 150000002367 halogens Chemical class 0.000 claims description 48
- 125000000623 heterocyclic group Chemical group 0.000 claims description 48
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 48
- 230000035772 mutation Effects 0.000 claims description 47
- 125000001424 substituent group Chemical group 0.000 claims description 45
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- 101710182396 Fibroblast growth factor receptor 3 Proteins 0.000 claims description 39
- 102100027842 Fibroblast growth factor receptor 3 Human genes 0.000 claims description 37
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 33
- ZEOWTGPWHLSLOG-UHFFFAOYSA-N Cc1ccc(cc1-c1ccc2c(n[nH]c2c1)-c1cnn(c1)C1CC1)C(=O)Nc1cccc(c1)C(F)(F)F Chemical compound Cc1ccc(cc1-c1ccc2c(n[nH]c2c1)-c1cnn(c1)C1CC1)C(=O)Nc1cccc(c1)C(F)(F)F ZEOWTGPWHLSLOG-UHFFFAOYSA-N 0.000 claims description 32
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- 101710182386 Fibroblast growth factor receptor 1 Proteins 0.000 claims description 32
- 239000012453 solvate Substances 0.000 claims description 30
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- 125000002950 monocyclic group Chemical group 0.000 claims description 29
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 29
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- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims description 27
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- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 18
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- 125000004432 carbon atom Chemical group C* 0.000 claims description 13
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- 125000002618 bicyclic heterocycle group Chemical group 0.000 claims description 12
- 239000000460 chlorine Chemical group 0.000 claims description 12
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 12
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- 125000004452 carbocyclyl group Chemical group 0.000 claims description 10
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- 229910007161 Si(CH3)3 Inorganic materials 0.000 claims description 8
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- 208000005718 Stomach Neoplasms Diseases 0.000 claims description 7
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims description 7
- 206010014733 Endometrial cancer Diseases 0.000 claims description 6
- 229910052799 carbon Inorganic materials 0.000 claims description 6
- 206010017758 gastric cancer Diseases 0.000 claims description 6
- 125000002757 morpholinyl group Chemical group 0.000 claims description 6
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- 208000000102 Squamous Cell Carcinoma of Head and Neck Diseases 0.000 claims description 4
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 4
- 239000011737 fluorine Chemical group 0.000 claims description 4
- 229910052731 fluorine Chemical group 0.000 claims description 4
- 208000002154 non-small cell lung carcinoma Diseases 0.000 claims description 4
- 201000002740 oral squamous cell carcinoma Diseases 0.000 claims description 4
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- 229910052801 chlorine Inorganic materials 0.000 claims description 3
- 230000005945 translocation Effects 0.000 claims description 3
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 2
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- 208000008839 Kidney Neoplasms Diseases 0.000 claims description 2
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- 125000003545 alkoxy group Chemical group 0.000 claims 2
- 208000029729 tumor suppressor gene on chromosome 11 Diseases 0.000 claims 2
- 201000000050 myeloid neoplasm Diseases 0.000 claims 1
- 238000000034 method Methods 0.000 abstract description 84
- 238000002360 preparation method Methods 0.000 abstract description 48
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- YEYHFKBVNARCNE-UHFFFAOYSA-N pyrido[2,3-b]pyrazine Chemical compound N1=CC=NC2=CC=CN=C21 YEYHFKBVNARCNE-UHFFFAOYSA-N 0.000 abstract description 2
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 187
- 239000000543 intermediate Substances 0.000 description 168
- 239000002904 solvent Substances 0.000 description 167
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 133
- 239000000203 mixture Substances 0.000 description 118
- 238000006243 chemical reaction Methods 0.000 description 97
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 91
- 102000044168 Fibroblast Growth Factor Receptor Human genes 0.000 description 75
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 69
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 59
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 55
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 52
- 239000002585 base Substances 0.000 description 52
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- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 44
- 239000000243 solution Substances 0.000 description 43
- 125000003118 aryl group Chemical group 0.000 description 42
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- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 28
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 28
- 108091000080 Phosphotransferase Proteins 0.000 description 24
- DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 24
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- 125000001072 heteroaryl group Chemical group 0.000 description 20
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Classifications
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- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
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- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
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Landscapes
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- Organic Chemistry (AREA)
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- Cardiology (AREA)
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- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Applications Claiming Priority (7)
| Application Number | Priority Date | Filing Date | Title |
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| US201261653140P | 2012-05-30 | 2012-05-30 | |
| US61/653,140 | 2012-05-30 | ||
| GBGB1209609.5A GB201209609D0 (en) | 2012-05-30 | 2012-05-30 | New compounds |
| GB1209609.5 | 2012-05-30 | ||
| US201361782210P | 2013-03-14 | 2013-03-14 | |
| US61/782,210 | 2013-03-14 | ||
| PCT/GB2013/051428 WO2013179034A1 (en) | 2012-05-30 | 2013-05-30 | New compounds |
Publications (2)
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| CA2874911A1 CA2874911A1 (en) | 2013-12-05 |
| CA2874911C true CA2874911C (en) | 2021-09-07 |
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| WO (1) | WO2013179034A1 (forum.php) |
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| GB201118652D0 (en) | 2011-10-28 | 2011-12-07 | Astex Therapeutics Ltd | New compounds |
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| GB201118675D0 (en) | 2011-10-28 | 2011-12-14 | Astex Therapeutics Ltd | New compounds |
| GB201118656D0 (en) | 2011-10-28 | 2011-12-07 | Astex Therapeutics Ltd | New compounds |
| GB201209613D0 (en) | 2012-05-30 | 2012-07-11 | Astex Therapeutics Ltd | New compounds |
| GB201209609D0 (en) | 2012-05-30 | 2012-07-11 | Astex Therapeutics Ltd | New compounds |
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| AR094812A1 (es) | 2013-02-20 | 2015-08-26 | Eisai R&D Man Co Ltd | Derivado de piridina monocíclico como inhibidor del fgfr |
| GB201307577D0 (en) | 2013-04-26 | 2013-06-12 | Astex Therapeutics Ltd | New compounds |
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