JP2007506744A5 - - Google Patents
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- JP2007506744A5 JP2007506744A5 JP2006528075A JP2006528075A JP2007506744A5 JP 2007506744 A5 JP2007506744 A5 JP 2007506744A5 JP 2006528075 A JP2006528075 A JP 2006528075A JP 2006528075 A JP2006528075 A JP 2006528075A JP 2007506744 A5 JP2007506744 A5 JP 2007506744A5
- Authority
- JP
- Japan
- Prior art keywords
- triazolo
- chloro
- trifluoro
- pyrimidin
- methylethyl
- 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.)
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- 150000003839 salts Chemical class 0.000 claims 59
- 150000001875 compounds Chemical class 0.000 claims 57
- 238000000034 method Methods 0.000 claims 18
- -1 3-Aminopropoxy Chemical group 0.000 claims 15
- 229910052739 hydrogen Inorganic materials 0.000 claims 12
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 10
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 8
- 239000002585 base Substances 0.000 claims 7
- 229910052799 carbon Inorganic materials 0.000 claims 7
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 7
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 claims 6
- 239000008194 pharmaceutical composition Substances 0.000 claims 6
- NTADARNNAPPIBY-UHFFFAOYSA-N triazolo[1,5-a]pyrimidin-7-amine Chemical compound NC1=CC=NC2=CN=NN12 NTADARNNAPPIBY-UHFFFAOYSA-N 0.000 claims 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 5
- 229910052757 nitrogen Inorganic materials 0.000 claims 5
- 102000004243 Tubulin Human genes 0.000 claims 4
- 108090000704 Tubulin Proteins 0.000 claims 4
- 238000002441 X-ray diffraction Methods 0.000 claims 4
- 150000001412 amines Chemical class 0.000 claims 4
- 239000000010 aprotic solvent Substances 0.000 claims 4
- 150000004683 dihydrates Chemical class 0.000 claims 4
- 125000000623 heterocyclic group Chemical group 0.000 claims 4
- 125000004430 oxygen atom Chemical group O* 0.000 claims 4
- 125000002572 propoxy group Chemical group [*]OC([H])([H])C(C([H])([H])[H])([H])[H] 0.000 claims 4
- 125000004434 sulfur atom Chemical group 0.000 claims 4
- TUXZQBYIZLWUKK-AFIAKLHKSA-N (e)-but-2-enedioic acid;5-chloro-6-[2,6-difluoro-4-[3-(methylamino)propoxy]phenyl]-n-[(2s)-1,1,1-trifluoropropan-2-yl]-[1,2,4]triazolo[1,5-a]pyrimidin-7-amine Chemical compound OC(=O)\C=C\C(O)=O.FC1=CC(OCCCNC)=CC(F)=C1C1=C(N[C@@H](C)C(F)(F)F)N2N=CN=C2N=C1Cl TUXZQBYIZLWUKK-AFIAKLHKSA-N 0.000 claims 3
- HAFUDZOLFLXVIY-FVGYRXGTSA-N 5-chloro-6-[2,6-difluoro-4-[3-(methylamino)propoxy]phenyl]-n-[(2s)-1,1,1-trifluoropropan-2-yl]-[1,2,4]triazolo[1,5-a]pyrimidin-7-amine;hydrochloride Chemical compound Cl.FC1=CC(OCCCNC)=CC(F)=C1C1=C(N[C@@H](C)C(F)(F)F)N2N=CN=C2N=C1Cl HAFUDZOLFLXVIY-FVGYRXGTSA-N 0.000 claims 3
- KPXQXVMQSPGTHL-BYPYZUCNSA-N 5-chloro-N-[(2S)-1,1,1-trifluoropropan-2-yl]-[1,2,4]triazolo[1,5-a]pyrimidin-7-amine Chemical compound ClC1=NC=2N(C(=C1)N[C@H](C(F)(F)F)C)N=CN=2 KPXQXVMQSPGTHL-BYPYZUCNSA-N 0.000 claims 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims 3
- QOXCEADXSTZKHA-UHFFFAOYSA-N [1,2,4]triazolo[1,5-a]pyrimidin-7-amine Chemical compound NC1=CC=NC2=NC=NN12 QOXCEADXSTZKHA-UHFFFAOYSA-N 0.000 claims 3
- OVAKAPOZRCLUHN-FVGYRXGTSA-N butanedioic acid;5-chloro-6-[2,6-difluoro-4-[3-(methylamino)propoxy]phenyl]-n-[(2s)-1,1,1-trifluoropropan-2-yl]-[1,2,4]triazolo[1,5-a]pyrimidin-7-amine Chemical compound OC(=O)CCC(O)=O.FC1=CC(OCCCNC)=CC(F)=C1C1=C(N[C@@H](C)C(F)(F)F)N2N=CN=C2N=C1Cl OVAKAPOZRCLUHN-FVGYRXGTSA-N 0.000 claims 3
- 125000000753 cycloalkyl group Chemical group 0.000 claims 3
- 125000000250 methylamino group Chemical group [H]N(*)C([H])([H])[H] 0.000 claims 3
- 230000036457 multidrug resistance Effects 0.000 claims 3
- 239000002904 solvent Substances 0.000 claims 3
- ZUZPCOQWSYNWLU-SECBINFHSA-N 5-chloro-6-[2,6-difluoro-4-[3-(methylamino)propoxy]phenyl]-n-[(2r)-1,1,1-trifluoropropan-2-yl]-[1,2,4]triazolo[1,5-a]pyrimidin-7-amine Chemical compound FC1=CC(OCCCNC)=CC(F)=C1C1=C(N[C@H](C)C(F)(F)F)N2N=CN=C2N=C1Cl ZUZPCOQWSYNWLU-SECBINFHSA-N 0.000 claims 2
- IAZDPXIOMUYVGZ-WFGJKAKNSA-N Dimethyl sulfoxide Chemical group [2H]C([2H])([2H])S(=O)C([2H])([2H])[2H] IAZDPXIOMUYVGZ-WFGJKAKNSA-N 0.000 claims 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims 2
- JGFZNNIVVJXRND-UHFFFAOYSA-N N,N-Diisopropylethylamine (DIPEA) Chemical group CCN(C(C)C)C(C)C JGFZNNIVVJXRND-UHFFFAOYSA-N 0.000 claims 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 claims 2
- 206010028980 Neoplasm Diseases 0.000 claims 2
- 239000002253 acid Substances 0.000 claims 2
- 229910000288 alkali metal carbonate Inorganic materials 0.000 claims 2
- 150000008041 alkali metal carbonates Chemical class 0.000 claims 2
- 150000008044 alkali metal hydroxides Chemical group 0.000 claims 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N dimethyl sulfoxide Natural products CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 claims 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N fumaric acid group Chemical group C(\C=C\C(=O)O)(=O)O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 claims 2
- 230000005764 inhibitory process Effects 0.000 claims 2
- 229910052760 oxygen Inorganic materials 0.000 claims 2
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 claims 2
- KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical compound OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 claims 2
- 229910052717 sulfur Inorganic materials 0.000 claims 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 2
- UUFXQPPJVCARJY-CBVSRFFLSA-N (e)-but-2-enedioic acid;5-chloro-6-[2,6-difluoro-4-[3-(methylamino)propoxy]phenyl]-n-[(2s)-1,1,1-trifluoropropan-2-yl]-[1,2,4]triazolo[1,5-a]pyrimidin-7-amine;dihydrate Chemical compound O.O.OC(=O)\C=C\C(O)=O.FC1=CC(OCCCNC)=CC(F)=C1C1=C(N[C@@H](C)C(F)(F)F)N2N=CN=C2N=C1Cl UUFXQPPJVCARJY-CBVSRFFLSA-N 0.000 claims 1
- XHWCCWGDJRYUJN-CGCSKFHYSA-N 1-[4-[5-chloro-7-[[(2R)-1,1,1-trifluoropropan-2-yl]amino]-[1,2,4]triazolo[1,5-a]pyrimidin-6-yl]-3,5-difluorophenyl]-N',N'-dimethylpropane-1,3-diamine Chemical compound ClC1=NC=2N(C(=C1C1=C(C=C(C=C1F)C(CCN(C)C)N)F)N[C@@H](C(F)(F)F)C)N=CN2 XHWCCWGDJRYUJN-CGCSKFHYSA-N 0.000 claims 1
- VKQKHTMZJLSQTG-IAPIXIRKSA-N 1-[4-[5-chloro-7-[[(2R)-1,1,1-trifluoropropan-2-yl]amino]-[1,2,4]triazolo[1,5-a]pyrimidin-6-yl]-3,5-difluorophenyl]-N,N',N'-trimethylpropane-1,3-diamine Chemical compound ClC1=NC=2N(C(=C1C1=C(C=C(C=C1F)C(CCN(C)C)NC)F)N[C@@H](C(F)(F)F)C)N=CN=2 VKQKHTMZJLSQTG-IAPIXIRKSA-N 0.000 claims 1
- MQLACMBJVPINKE-UHFFFAOYSA-N 10-[(3-hydroxy-4-methoxyphenyl)methylidene]anthracen-9-one Chemical compound C1=C(O)C(OC)=CC=C1C=C1C2=CC=CC=C2C(=O)C2=CC=CC=C21 MQLACMBJVPINKE-UHFFFAOYSA-N 0.000 claims 1
- LQUQZWNUVMXWOH-SSDOTTSWSA-N 2-[4-[5-chloro-7-[[(2r)-1,1,1-trifluoropropan-2-yl]amino]-[1,2,4]triazolo[1,5-a]pyrimidin-6-yl]-3,5-difluorophenoxy]ethanol Chemical compound ClC1=NC2=NC=NN2C(N[C@H](C)C(F)(F)F)=C1C1=C(F)C=C(OCCO)C=C1F LQUQZWNUVMXWOH-SSDOTTSWSA-N 0.000 claims 1
- GINJNNGWMNSBIG-UHFFFAOYSA-N 2-n-methylpropane-1,2-diamine Chemical compound CNC(C)CN GINJNNGWMNSBIG-UHFFFAOYSA-N 0.000 claims 1
- SILNEJLZHQBBBR-UHFFFAOYSA-N 3-[4-(5-chloro-7-cycloheptyl-[1,2,4]triazolo[1,5-a]pyrimidin-6-yl)-3,5-difluorophenoxy]propan-1-ol Chemical compound FC1=CC(OCCCO)=CC(F)=C1C1=C(C2CCCCCC2)N2N=CN=C2N=C1Cl SILNEJLZHQBBBR-UHFFFAOYSA-N 0.000 claims 1
- PYOBBMDUGURFMC-MRVPVSSYSA-N 3-[4-[5-chloro-7-[[(2r)-1,1,1-trifluoropropan-2-yl]amino]-[1,2,4]triazolo[1,5-a]pyrimidin-6-yl]-3,5-difluorophenoxy]propan-1-ol Chemical compound ClC1=NC2=NC=NN2C(N[C@H](C)C(F)(F)F)=C1C1=C(F)C=C(OCCCO)C=C1F PYOBBMDUGURFMC-MRVPVSSYSA-N 0.000 claims 1
- TURWXBQPPKQQIC-UHFFFAOYSA-N 4-[4-(4-oxobutylamino)butylamino]butanal Chemical compound O=CCCCNCCCCNCCCC=O TURWXBQPPKQQIC-UHFFFAOYSA-N 0.000 claims 1
- NSIRLJFAZOCMEI-SECBINFHSA-N 4-[4-[5-chloro-7-[[(2r)-1,1,1-trifluoropropan-2-yl]amino]-[1,2,4]triazolo[1,5-a]pyrimidin-6-yl]-3,5-difluorophenoxy]butan-1-ol Chemical compound ClC1=NC2=NC=NN2C(N[C@H](C)C(F)(F)F)=C1C1=C(F)C=C(OCCCCO)C=C1F NSIRLJFAZOCMEI-SECBINFHSA-N 0.000 claims 1
- 125000004195 4-methylpiperazin-1-yl group Chemical group [H]C([H])([H])N1C([H])([H])C([H])([H])N(*)C([H])([H])C1([H])[H] 0.000 claims 1
- VFFSFDFJZAYCBT-SNVBAGLBSA-N 5-bromo-6-[4-[3-(dimethylamino)propoxy]-2,6-difluorophenyl]-n-[(2r)-1,1,1-trifluoropropan-2-yl]-[1,2,4]triazolo[1,5-a]pyrimidin-7-amine Chemical compound BrC1=NC2=NC=NN2C(N[C@H](C)C(F)(F)F)=C1C1=C(F)C=C(OCCCN(C)C)C=C1F VFFSFDFJZAYCBT-SNVBAGLBSA-N 0.000 claims 1
- VFFSFDFJZAYCBT-JTQLQIEISA-N 5-bromo-6-[4-[3-(dimethylamino)propoxy]-2,6-difluorophenyl]-n-[(2s)-1,1,1-trifluoropropan-2-yl]-[1,2,4]triazolo[1,5-a]pyrimidin-7-amine Chemical compound BrC1=NC2=NC=NN2C(N[C@@H](C)C(F)(F)F)=C1C1=C(F)C=C(OCCCN(C)C)C=C1F VFFSFDFJZAYCBT-JTQLQIEISA-N 0.000 claims 1
- MIZWZYPKIVHIRV-LLVKDONJSA-N 5-chloro-6-[2,6-difluoro-4-(2-morpholin-4-ylethoxy)phenyl]-n-[(2r)-1,1,1-trifluoropropan-2-yl]-[1,2,4]triazolo[1,5-a]pyrimidin-7-amine Chemical compound ClC1=NC2=NC=NN2C(N[C@H](C)C(F)(F)F)=C1C(C(=C1)F)=C(F)C=C1OCCN1CCOCC1 MIZWZYPKIVHIRV-LLVKDONJSA-N 0.000 claims 1
- MIZWZYPKIVHIRV-NSHDSACASA-N 5-chloro-6-[2,6-difluoro-4-(2-morpholin-4-ylethoxy)phenyl]-n-[(2s)-1,1,1-trifluoropropan-2-yl]-[1,2,4]triazolo[1,5-a]pyrimidin-7-amine Chemical compound ClC1=NC2=NC=NN2C(N[C@@H](C)C(F)(F)F)=C1C(C(=C1)F)=C(F)C=C1OCCN1CCOCC1 MIZWZYPKIVHIRV-NSHDSACASA-N 0.000 claims 1
- QKXFUKJAICMMGW-GFCCVEGCSA-N 5-chloro-6-[2,6-difluoro-4-(3-morpholin-4-ylpropoxy)phenyl]-n-[(2r)-1,1,1-trifluoropropan-2-yl]-[1,2,4]triazolo[1,5-a]pyrimidin-7-amine Chemical compound ClC1=NC2=NC=NN2C(N[C@H](C)C(F)(F)F)=C1C(C(=C1)F)=C(F)C=C1OCCCN1CCOCC1 QKXFUKJAICMMGW-GFCCVEGCSA-N 0.000 claims 1
- UWVYORNWUVNEHV-CYBMUJFWSA-N 5-chloro-6-[2,6-difluoro-4-(3-piperidin-1-ylpropoxy)phenyl]-n-[(2r)-1,1,1-trifluoropropan-2-yl]-[1,2,4]triazolo[1,5-a]pyrimidin-7-amine Chemical compound ClC1=NC2=NC=NN2C(N[C@H](C)C(F)(F)F)=C1C(C(=C1)F)=C(F)C=C1OCCCN1CCCCC1 UWVYORNWUVNEHV-CYBMUJFWSA-N 0.000 claims 1
- MEZUNAKNPOIBGG-GFCCVEGCSA-N 5-chloro-6-[2,6-difluoro-4-(3-pyrrolidin-1-ylpropoxy)phenyl]-n-[(2r)-1,1,1-trifluoropropan-2-yl]-[1,2,4]triazolo[1,5-a]pyrimidin-7-amine Chemical compound ClC1=NC2=NC=NN2C(N[C@H](C)C(F)(F)F)=C1C(C(=C1)F)=C(F)C=C1OCCCN1CCCC1 MEZUNAKNPOIBGG-GFCCVEGCSA-N 0.000 claims 1
- ZYLQMJCSPMXOHL-MRVPVSSYSA-N 5-chloro-6-[2,6-difluoro-4-[2-(methylamino)ethoxy]phenyl]-n-[(2r)-1,1,1-trifluoropropan-2-yl]-[1,2,4]triazolo[1,5-a]pyrimidin-7-amine Chemical compound FC1=CC(OCCNC)=CC(F)=C1C1=C(N[C@H](C)C(F)(F)F)N2N=CN=C2N=C1Cl ZYLQMJCSPMXOHL-MRVPVSSYSA-N 0.000 claims 1
- ZYLQMJCSPMXOHL-QMMMGPOBSA-N 5-chloro-6-[2,6-difluoro-4-[2-(methylamino)ethoxy]phenyl]-n-[(2s)-1,1,1-trifluoropropan-2-yl]-[1,2,4]triazolo[1,5-a]pyrimidin-7-amine Chemical compound FC1=CC(OCCNC)=CC(F)=C1C1=C(N[C@@H](C)C(F)(F)F)N2N=CN=C2N=C1Cl ZYLQMJCSPMXOHL-QMMMGPOBSA-N 0.000 claims 1
- ZAJCZMAIPRGPFP-CYBMUJFWSA-N 5-chloro-6-[2,6-difluoro-4-[3-(4-methylpiperazin-1-yl)propoxy]phenyl]-n-[(2r)-1,1,1-trifluoropropan-2-yl]-[1,2,4]triazolo[1,5-a]pyrimidin-7-amine Chemical compound ClC1=NC2=NC=NN2C(N[C@H](C)C(F)(F)F)=C1C(C(=C1)F)=C(F)C=C1OCCCN1CCN(C)CC1 ZAJCZMAIPRGPFP-CYBMUJFWSA-N 0.000 claims 1
- GHMHOHRZRISOHU-UHFFFAOYSA-N 5-chloro-6-[2,6-difluoro-4-[3-(methylamino)propoxy]phenyl]-n-(2,2,2-trifluoroethyl)-[1,2,4]triazolo[1,5-a]pyrimidin-7-amine Chemical compound FC1=CC(OCCCNC)=CC(F)=C1C1=C(NCC(F)(F)F)N2N=CN=C2N=C1Cl GHMHOHRZRISOHU-UHFFFAOYSA-N 0.000 claims 1
- JNSFRMDQQFZFBJ-CYBMUJFWSA-N 5-chloro-6-[2,6-difluoro-4-[3-(methylamino)propoxy]phenyl]-n-[(2r)-1,1,1-trifluorobutan-2-yl]-[1,2,4]triazolo[1,5-a]pyrimidin-7-amine Chemical compound ClC1=NC2=NC=NN2C(N[C@H](CC)C(F)(F)F)=C1C1=C(F)C=C(OCCCNC)C=C1F JNSFRMDQQFZFBJ-CYBMUJFWSA-N 0.000 claims 1
- ZUZPCOQWSYNWLU-VIFPVBQESA-N 5-chloro-6-[2,6-difluoro-4-[3-(methylamino)propoxy]phenyl]-n-[(2s)-1,1,1-trifluoropropan-2-yl]-[1,2,4]triazolo[1,5-a]pyrimidin-7-amine Chemical compound FC1=CC(OCCCNC)=CC(F)=C1C1=C(N[C@@H](C)C(F)(F)F)N2N=CN=C2N=C1Cl ZUZPCOQWSYNWLU-VIFPVBQESA-N 0.000 claims 1
- XAKKESNRKUXRPK-SECBINFHSA-N 5-chloro-6-[3-[2-(dimethylamino)ethoxy]-2,6-difluorophenyl]-n-[(2r)-1,1,1-trifluoropropan-2-yl]-[1,2,4]triazolo[1,5-a]pyrimidin-7-amine Chemical compound ClC1=NC2=NC=NN2C(N[C@H](C)C(F)(F)F)=C1C1=C(F)C=CC(OCCN(C)C)=C1F XAKKESNRKUXRPK-SECBINFHSA-N 0.000 claims 1
- XAKKESNRKUXRPK-VIFPVBQESA-N 5-chloro-6-[3-[2-(dimethylamino)ethoxy]-2,6-difluorophenyl]-n-[(2s)-1,1,1-trifluoropropan-2-yl]-[1,2,4]triazolo[1,5-a]pyrimidin-7-amine Chemical compound ClC1=NC2=NC=NN2C(N[C@@H](C)C(F)(F)F)=C1C1=C(F)C=CC(OCCN(C)C)=C1F XAKKESNRKUXRPK-VIFPVBQESA-N 0.000 claims 1
- GXPIFHVEFPCZPS-SNVBAGLBSA-N 5-chloro-6-[3-[3-(dimethylamino)propoxy]-2,6-difluorophenyl]-n-[(2r)-1,1,1-trifluoropropan-2-yl]-[1,2,4]triazolo[1,5-a]pyrimidin-7-amine Chemical compound ClC1=NC2=NC=NN2C(N[C@H](C)C(F)(F)F)=C1C1=C(F)C=CC(OCCCN(C)C)=C1F GXPIFHVEFPCZPS-SNVBAGLBSA-N 0.000 claims 1
- GXPIFHVEFPCZPS-JTQLQIEISA-N 5-chloro-6-[3-[3-(dimethylamino)propoxy]-2,6-difluorophenyl]-n-[(2s)-1,1,1-trifluoropropan-2-yl]-[1,2,4]triazolo[1,5-a]pyrimidin-7-amine Chemical compound ClC1=NC2=NC=NN2C(N[C@@H](C)C(F)(F)F)=C1C1=C(F)C=CC(OCCCN(C)C)=C1F GXPIFHVEFPCZPS-JTQLQIEISA-N 0.000 claims 1
- QHBMOSBSGXNWHS-LLVKDONJSA-N 5-chloro-6-[3-[4-(dimethylamino)butoxy]-2,6-difluorophenyl]-n-[(2r)-1,1,1-trifluoropropan-2-yl]-[1,2,4]triazolo[1,5-a]pyrimidin-7-amine Chemical compound ClC1=NC2=NC=NN2C(N[C@H](C)C(F)(F)F)=C1C1=C(F)C=CC(OCCCCN(C)C)=C1F QHBMOSBSGXNWHS-LLVKDONJSA-N 0.000 claims 1
- QHBMOSBSGXNWHS-NSHDSACASA-N 5-chloro-6-[3-[4-(dimethylamino)butoxy]-2,6-difluorophenyl]-n-[(2s)-1,1,1-trifluoropropan-2-yl]-[1,2,4]triazolo[1,5-a]pyrimidin-7-amine Chemical compound ClC1=NC2=NC=NN2C(N[C@@H](C)C(F)(F)F)=C1C1=C(F)C=CC(OCCCCN(C)C)=C1F QHBMOSBSGXNWHS-NSHDSACASA-N 0.000 claims 1
- FDKOUKLCYAUQES-SECBINFHSA-N 5-chloro-6-[4-[2-(dimethylamino)ethoxy]-2,6-difluorophenyl]-n-[(2r)-1,1,1-trifluoropropan-2-yl]-[1,2,4]triazolo[1,5-a]pyrimidin-7-amine Chemical compound ClC1=NC2=NC=NN2C(N[C@H](C)C(F)(F)F)=C1C1=C(F)C=C(OCCN(C)C)C=C1F FDKOUKLCYAUQES-SECBINFHSA-N 0.000 claims 1
- FDKOUKLCYAUQES-VIFPVBQESA-N 5-chloro-6-[4-[2-(dimethylamino)ethoxy]-2,6-difluorophenyl]-n-[(2s)-1,1,1-trifluoropropan-2-yl]-[1,2,4]triazolo[1,5-a]pyrimidin-7-amine Chemical compound ClC1=NC2=NC=NN2C(N[C@@H](C)C(F)(F)F)=C1C1=C(F)C=C(OCCN(C)C)C=C1F FDKOUKLCYAUQES-VIFPVBQESA-N 0.000 claims 1
- UYUJACMPNPNLMY-UHFFFAOYSA-N 5-chloro-6-[4-[3-(dimethylamino)propoxy]-2,6-difluorophenyl]-n-(2,2,2-trifluoroethyl)-[1,2,4]triazolo[1,5-a]pyrimidin-7-amine Chemical compound FC1=CC(OCCCN(C)C)=CC(F)=C1C1=C(NCC(F)(F)F)N2N=CN=C2N=C1Cl UYUJACMPNPNLMY-UHFFFAOYSA-N 0.000 claims 1
- ZSLWBWNJXMEWNY-SNVBAGLBSA-N 5-chloro-6-[4-[3-(dimethylamino)propoxy]-2,6-difluorophenyl]-n-[(2r)-1,1,1-trifluoropropan-2-yl]-[1,2,4]triazolo[1,5-a]pyrimidin-7-amine Chemical compound ClC1=NC2=NC=NN2C(N[C@H](C)C(F)(F)F)=C1C1=C(F)C=C(OCCCN(C)C)C=C1F ZSLWBWNJXMEWNY-SNVBAGLBSA-N 0.000 claims 1
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- YTOAWZMMRBSRKF-JTQLQIEISA-N 5-chloro-6-[4-[3-(ethylamino)propoxy]-2,6-difluorophenyl]-n-[(2s)-1,1,1-trifluoropropan-2-yl]-[1,2,4]triazolo[1,5-a]pyrimidin-7-amine Chemical compound FC1=CC(OCCCNCC)=CC(F)=C1C1=C(N[C@@H](C)C(F)(F)F)N2N=CN=C2N=C1Cl YTOAWZMMRBSRKF-JTQLQIEISA-N 0.000 claims 1
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- 210000004881 tumor cell Anatomy 0.000 claims 1
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| US6255309B1 (en) * | 1999-03-19 | 2001-07-03 | American Cyanomid Co. | Fungicidal trifluoromethylalkylamino-triazolopyrimidines |
| JP2004502691A (ja) * | 2000-06-30 | 2004-01-29 | ワイス | 抗癌薬としての置換トリアゾロピリミジン |
| US7419982B2 (en) * | 2003-09-24 | 2008-09-02 | Wyeth Holdings Corporation | Crystalline forms of 5-chloro-6-{2,6-difluoro-4-[3-(methylamino)propoxy]phenyl}-N-[(1S)-2,2,2-trifluoro-1-methylethyl][1,2,4]triazolo[1,5-a]pyrimidin-7-amine salts |
| BRPI0414700A (pt) | 2003-09-24 | 2006-11-14 | Wyeth Corp | 6-[(substituìdo)fenil]triazolopirimidinas como agentes anti-cáncer |
| MY179926A (en) * | 2003-12-08 | 2020-11-19 | Wyeth Corp | Process for the preparation of tubulin inhibitors |
| EP1891052A1 (en) * | 2005-06-13 | 2008-02-27 | Wyeth | Tubulin inhibitor and process for its preparation |
| CN101193884A (zh) | 2005-06-13 | 2008-06-04 | 惠氏公司 | 微管蛋白抑制剂和其制备方法 |
| CN101208289A (zh) * | 2005-06-27 | 2008-06-25 | 巴斯福股份公司 | 生产取代的苯基丙二酸酯中间体化合物的方法及其在生产5,7-二羟基-6-(2,4,6-三氟苯基)[1,2,4]三唑并[1,5-a]嘧啶中的用途 |
| WO2007075465A1 (en) * | 2005-12-16 | 2007-07-05 | Wyeth | Dimers and adducts of 6-[(substituted) phenyl] triazolopyrimidines useful as anticancer agents |
| TW200730530A (en) * | 2005-12-16 | 2007-08-16 | Wyeth Corp | Lyophilized compositions of a triazolopyrimidine compound |
| CN101600350A (zh) * | 2007-01-08 | 2009-12-09 | 巴斯夫欧洲公司 | 唑并嘧啶在防治植物病原性有害真菌中的用途 |
| WO2014047257A2 (en) | 2012-09-19 | 2014-03-27 | The Trustees Of The University Of Pennsylvania | Heterocyclic compounds and their use for the treatment of neurodegenerative tauopathies |
| WO2019169111A1 (en) | 2018-03-02 | 2019-09-06 | The Trustees Of The University Of Pennsylvania | [1,2,4]triazolo[1,5-a]pyrimidine compounds and use in stabilizing microtubules |
| AU2021255495A1 (en) * | 2020-04-14 | 2022-12-15 | The Regents Of The University Of California | Substituted {1,2,4,} triazolo{1,5-a} pyrimidine compounds and use in stabilizing microtubules |
| CN114369098B (zh) * | 2022-01-06 | 2023-03-10 | 苏州大学 | 一种三唑并嘧啶醇类化合物及其制备方法和应用 |
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| DE69914364T2 (de) | 1998-09-25 | 2004-07-22 | Basf Ag | Nicht-wässriges suspensionskonzentrat |
| SI0988790T1 (en) | 1998-09-25 | 2003-10-31 | Basf Aktiengesellschaft | Fungicidal mixtures |
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-
2004
- 2004-09-17 BR BRPI0414700-6A patent/BRPI0414700A/pt not_active IP Right Cessation
- 2004-09-17 PL PL04788820T patent/PL1680425T3/pl unknown
- 2004-09-17 ES ES04788820T patent/ES2279452T3/es not_active Expired - Lifetime
- 2004-09-17 CA CA002539252A patent/CA2539252A1/en not_active Abandoned
- 2004-09-17 RU RU2006107579/04A patent/RU2006107579A/ru not_active Application Discontinuation
- 2004-09-17 EP EP04788820A patent/EP1680425B1/en not_active Expired - Lifetime
- 2004-09-17 PT PT04788820T patent/PT1680425E/pt unknown
- 2004-09-17 SI SI200430195T patent/SI1680425T1/sl unknown
- 2004-09-17 CN CNB2004800302006A patent/CN100519559C/zh not_active Expired - Fee Related
- 2004-09-17 AU AU2004276240A patent/AU2004276240A1/en not_active Withdrawn
- 2004-09-17 KR KR1020067005785A patent/KR20060098368A/ko not_active Withdrawn
- 2004-09-17 MX MXPA06003206A patent/MXPA06003206A/es active IP Right Grant
- 2004-09-17 DK DK04788820T patent/DK1680425T3/da active
- 2004-09-17 DE DE602004004295T patent/DE602004004295T8/de active Active
- 2004-09-17 JP JP2006528075A patent/JP2007506744A/ja not_active Withdrawn
- 2004-09-17 WO PCT/US2004/030515 patent/WO2005030775A1/en not_active Ceased
- 2004-09-21 TW TW093128500A patent/TW200512211A/zh unknown
- 2004-09-22 SA SA04250302A patent/SA04250302A/ar unknown
- 2004-09-23 AR ARP040103440A patent/AR045810A1/es not_active Application Discontinuation
- 2004-09-23 PE PE2004000925A patent/PE20050433A1/es not_active Application Discontinuation
- 2004-09-24 PA PA20048613301A patent/PA8613301A1/es unknown
- 2004-09-24 GT GT200400190A patent/GT200400190A/es unknown
- 2004-09-24 US US10/950,543 patent/US7507739B2/en not_active Expired - Fee Related
-
2006
- 2006-03-13 IL IL174281A patent/IL174281A0/en unknown
- 2006-03-14 CR CR8288A patent/CR8288A/es not_active Application Discontinuation
- 2006-03-23 NO NO20061318A patent/NO20061318L/no not_active Application Discontinuation
- 2006-03-23 ZA ZA200602387A patent/ZA200602387B/xx unknown
- 2006-03-24 EC EC2006006458A patent/ECSP066458A/es unknown
- 2006-04-21 CO CO06038133A patent/CO5690598A2/es not_active Application Discontinuation
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2007
- 2007-03-16 CY CY20071100373T patent/CY1106392T1/el unknown
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