SK4142003A3 - Substituted 3,4-dihydro-pyrido[1,2-A]pyrimidines, process for producing thereof, medicaments comprising same and their use - Google Patents

Substituted 3,4-dihydro-pyrido[1,2-A]pyrimidines, process for producing thereof, medicaments comprising same and their use Download PDF

Info

Publication number: SK4142003A3
Authority: SK; Slovakia
Prior art keywords: unsubstituted; substituted; alkyl; mono; poly
Prior art date: 2000-10-13

Application number

SK414-2003A

Other languages

English (en)

Slovak (sk)

Inventor

Matthias Gerlach

Corinna Sundermann

Utz-Peter Jagusch

Original Assignee

Gruenenthal Chemie

Priority date (The priority date 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 date listed.)

2000-10-13

Filing date

2001-10-10

Publication date

2003-10-07

2001-10-10 Application filed by Gruenenthal Chemie filed Critical Gruenenthal Chemie

2003-10-07 Publication of SK4142003A3 publication Critical patent/SK4142003A3/sk

Links

238000000034 method Methods 0.000 title claims abstract description 30
239000003814 drug Substances 0.000 title claims abstract description 22
WJEHYVLQWVIEJM-UHFFFAOYSA-N 3,4-dihydro-2h-pyrido[1,2-a]pyrimidine Chemical class C1=CC=CN2CCCN=C21 WJEHYVLQWVIEJM-UHFFFAOYSA-N 0.000 title claims description 15
150000001875 compounds Chemical class 0.000 claims abstract description 147
208000002193 Pain Diseases 0.000 claims abstract description 15
230000036407 pain Effects 0.000 claims abstract description 12
238000004519 manufacturing process Methods 0.000 claims abstract description 9
206010012735 Diarrhoea Diseases 0.000 claims abstract description 7
208000009205 Tinnitus Diseases 0.000 claims abstract description 7
206010046543 Urinary incontinence Diseases 0.000 claims abstract description 7
231100000886 tinnitus Toxicity 0.000 claims abstract description 7
239000000825 pharmaceutical preparation Substances 0.000 claims abstract description 4
125000000217 alkyl group Chemical group 0.000 claims description 654
229920006395 saturated elastomer Polymers 0.000 claims description 461
125000004432 carbon atom Chemical group C* 0.000 claims description 337
125000003118 aryl group Chemical group 0.000 claims description 321
125000001072 heteroaryl group Chemical class 0.000 claims description 217
125000000753 cycloalkyl group Chemical group 0.000 claims description 191
125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 165
-1 OR 10 Chemical class 0.000 claims description 133
229910052799 carbon Inorganic materials 0.000 claims description 117
125000002877 alkyl aryl group Chemical group 0.000 claims description 112
125000003107 substituted aryl group Chemical group 0.000 claims description 100
239000001257 hydrogen Substances 0.000 claims description 77
229910052739 hydrogen Inorganic materials 0.000 claims description 77
125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 70
150000003254 radicals Chemical class 0.000 claims description 64
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 57
239000004743 Polypropylene Substances 0.000 claims description 50
125000005213 alkyl heteroaryl group Chemical group 0.000 claims description 42
125000004172 4-methoxyphenyl group Chemical group [H]C1=C([H])C(OC([H])([H])[H])=C([H])C([H])=C1* 0.000 claims description 39
125000000623 heterocyclic group Chemical group 0.000 claims description 39
125000004890 (C1-C6) alkylamino group Chemical group 0.000 claims description 36
125000006619 (C1-C6) dialkylamino group Chemical group 0.000 claims description 35
125000000246 pyrimidin-2-yl group Chemical group [H]C1=NC(*)=NC([H])=C1[H] 0.000 claims description 34
150000003839 salts Chemical class 0.000 claims description 34
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 33
239000000460 chlorine Substances 0.000 claims description 33
229910052801 chlorine Inorganic materials 0.000 claims description 33
229910052731 fluorine Inorganic materials 0.000 claims description 32
125000004093 cyano group Chemical group *C#N 0.000 claims description 31
125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims description 29
PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 29
239000011737 fluorine Substances 0.000 claims description 29
CYRMSUTZVYGINF-UHFFFAOYSA-N trichlorofluoromethane Chemical compound FC(Cl)(Cl)Cl CYRMSUTZVYGINF-UHFFFAOYSA-N 0.000 claims description 28
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 26
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 26
229910052794 bromium Inorganic materials 0.000 claims description 26
125000004947 alkyl aryl amino group Chemical group 0.000 claims description 24
125000003762 3,4-dimethoxyphenyl group Chemical group [H]C1=C([H])C(OC([H])([H])[H])=C(OC([H])([H])[H])C([H])=C1* 0.000 claims description 21
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 21
125000004209 (C1-C8) alkyl group Chemical group 0.000 claims description 20
239000002253 acid Substances 0.000 claims description 20
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 18
125000001153 fluoro group Chemical group F* 0.000 claims description 16
125000005241 heteroarylamino group Chemical group 0.000 claims description 16
WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical group CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 claims description 15
125000001246 bromo group Chemical group Br* 0.000 claims description 14
125000001309 chloro group Chemical group Cl* 0.000 claims description 14
125000004494 ethyl ester group Chemical group 0.000 claims description 13
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 13
239000000203 mixture Substances 0.000 claims description 12
125000006239 protecting group Chemical group 0.000 claims description 12
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 11
PXQLVRUNWNTZOS-UHFFFAOYSA-N sulfanyl Chemical class [SH] PXQLVRUNWNTZOS-UHFFFAOYSA-N 0.000 claims description 11
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 10
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 10
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 10
GVNVAWHJIKLAGL-UHFFFAOYSA-N 2-(cyclohexen-1-yl)cyclohexan-1-one Chemical compound O=C1CCCCC1C1=CCCCC1 GVNVAWHJIKLAGL-UHFFFAOYSA-N 0.000 claims description 9
101150065749 Churc1 gene Proteins 0.000 claims description 9
102100038239 Protein Churchill Human genes 0.000 claims description 9
150000001336 alkenes Chemical class 0.000 claims description 9
238000006243 chemical reaction Methods 0.000 claims description 9
JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 claims description 9
238000002360 preparation method Methods 0.000 claims description 9
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 claims description 8
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 8
229910052760 oxygen Inorganic materials 0.000 claims description 8
229910052717 sulfur Inorganic materials 0.000 claims description 8
125000004203 4-hydroxyphenyl group Chemical group [H]OC1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 7
KHCIECWGKIRMER-UHFFFAOYSA-N 9-chloro-4-(4-methoxyphenyl)-3-methyl-7-(trifluoromethyl)-3,4-dihydro-2h-pyrido[1,2-a]pyrimidine-2-carboxylic acid Chemical compound C1=CC(OC)=CC=C1C1N(C=C(C=C2Cl)C(F)(F)F)C2=NC(C(O)=O)C1C KHCIECWGKIRMER-UHFFFAOYSA-N 0.000 claims description 7
KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 claims description 7
AGEJVIVJCSOOTF-UHFFFAOYSA-N 4-(3,4-dimethoxyphenyl)-7-nitro-3,4-dihydro-2h-pyrido[1,2-a]pyrimidine-2-carboxylic acid Chemical compound C1=C(OC)C(OC)=CC=C1C1N2C=C([N+]([O-])=O)C=CC2=NC(C(O)=O)C1 AGEJVIVJCSOOTF-UHFFFAOYSA-N 0.000 claims description 6
KFYMGQHIQYEPNT-UHFFFAOYSA-N 7,9-dibromo-4-(4-methoxyphenyl)-3-methyl-3,4-dihydro-2h-pyrido[1,2-a]pyrimidine-2-carboxylic acid Chemical compound C1=CC(OC)=CC=C1C1N(C=C(Br)C=C2Br)C2=NC(C(O)=O)C1C KFYMGQHIQYEPNT-UHFFFAOYSA-N 0.000 claims description 6
HUWQRRIZLURENZ-UHFFFAOYSA-N 7,9-dichloro-4-(3,4-dimethoxyphenyl)-3,4-dihydro-2h-pyrido[1,2-a]pyrimidine-2-carboxylic acid Chemical compound C1=C(OC)C(OC)=CC=C1C1N(C=C(Cl)C=C2Cl)C2=NC(C(O)=O)C1 HUWQRRIZLURENZ-UHFFFAOYSA-N 0.000 claims description 6
208000003251 Pruritus Diseases 0.000 claims description 6
DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 claims description 6
150000001299 aldehydes Chemical class 0.000 claims description 6
UKGRURSIMJQIMJ-UHFFFAOYSA-N 4-(4-methoxyphenyl)-7-nitro-3,4-dihydro-2h-pyrido[1,2-a]pyrimidine-2-carboxylic acid Chemical compound C1=CC(OC)=CC=C1C1N2C=C([N+]([O-])=O)C=CC2=NC(C(O)=O)C1 UKGRURSIMJQIMJ-UHFFFAOYSA-N 0.000 claims description 5
IVTDWFYNZWWHFQ-UHFFFAOYSA-N 7,9-dibromo-4-(3,4-dimethoxyphenyl)-6-methyl-3,4-dihydro-2h-pyrido[1,2-a]pyrimidine-2-carboxylic acid Chemical compound C1=C(OC)C(OC)=CC=C1C1N(C(C)=C(Br)C=C2Br)C2=NC(C(O)=O)C1 IVTDWFYNZWWHFQ-UHFFFAOYSA-N 0.000 claims description 5
230000007803 itching Effects 0.000 claims description 5
239000000546 pharmaceutical excipient Substances 0.000 claims description 5
ZFCHNZDUMIOWFV-UHFFFAOYSA-N pyrimidine-2-carboxylic acid Chemical compound OC(=O)C1=NC=CC=N1 ZFCHNZDUMIOWFV-UHFFFAOYSA-N 0.000 claims description 5
125000001622 2-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C([H])=C(*)C([H])=C([H])C2=C1[H] 0.000 claims description 4
125000004429 atom Chemical group 0.000 claims description 4
150000001721 carbon Chemical group 0.000 claims description 4
125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 4
YMGUBTXCNDTFJI-UHFFFAOYSA-N cyclopropanecarboxylic acid Chemical compound OC(=O)C1CC1 YMGUBTXCNDTFJI-UHFFFAOYSA-N 0.000 claims description 4
239000003960 organic solvent Substances 0.000 claims description 4
125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 3
IHAZKYDIMJCCIK-UHFFFAOYSA-N 2-(2-nitrophenyl)-4-phenyl-3,4-dihydro-2h-pyrido[1,2-a]pyrimidine Chemical compound [O-][N+](=O)C1=CC=CC=C1C1N=C2C=CC=CN2C(C=2C=CC=CC=2)C1 IHAZKYDIMJCCIK-UHFFFAOYSA-N 0.000 claims description 3
XDQQJWMETYQVKG-UHFFFAOYSA-N 2-(4-chlorophenyl)-4-(4-methylphenyl)-3,4-dihydro-2h-pyrido[1,2-a]pyrimidine Chemical compound C1=CC(C)=CC=C1C1N2C=CC=CC2=NC(C=2C=CC(Cl)=CC=2)C1 XDQQJWMETYQVKG-UHFFFAOYSA-N 0.000 claims description 3
OMMUPTFVHSUBPU-UHFFFAOYSA-N 2-(4-ethoxy-3,4-dihydro-2h-pyrido[1,2-a]pyrimidin-2-yl)phenol Chemical compound N1=C2C=CC=CN2C(OCC)CC1C1=CC=CC=C1O OMMUPTFVHSUBPU-UHFFFAOYSA-N 0.000 claims description 3
LWBRHDPNARNWBQ-UHFFFAOYSA-N 2-(4-nitrophenyl)-4-phenyl-3,4-dihydro-2h-pyrido[1,2-a]pyrimidine Chemical compound C1=CC([N+](=O)[O-])=CC=C1C1N=C2C=CC=CN2C(C=2C=CC=CC=2)C1 LWBRHDPNARNWBQ-UHFFFAOYSA-N 0.000 claims description 3
XDKDXXVWGPRGGY-UHFFFAOYSA-N 2-[(2-cyclohexyl-7-nitro-3,4-dihydro-2h-pyrido[1,2-a]pyrimidin-4-yl)oxy]ethanol Chemical compound N1=C2C=CC([N+]([O-])=O)=CN2C(OCCO)CC1C1CCCCC1 XDKDXXVWGPRGGY-UHFFFAOYSA-N 0.000 claims description 3
ZHYJFQHQZFIQBN-UHFFFAOYSA-N 2-[(2-cyclopropyl-7-nitro-3,4-dihydro-2h-pyrido[1,2-a]pyrimidin-4-yl)oxy]ethanol Chemical compound N1=C2C=CC([N+]([O-])=O)=CN2C(OCCO)CC1C1CC1 ZHYJFQHQZFIQBN-UHFFFAOYSA-N 0.000 claims description 3
NKTLKJWRRHSDJK-UHFFFAOYSA-N 2-[(7,9-dibromo-2-cyclohexyl-3,4-dihydro-2h-pyrido[1,2-a]pyrimidin-4-yl)oxy]ethanol Chemical compound N1=C(C(=CC(Br)=C2)Br)N2C(OCCO)CC1C1CCCCC1 NKTLKJWRRHSDJK-UHFFFAOYSA-N 0.000 claims description 3
YAJHBJGCFLKFPH-UHFFFAOYSA-N 2-[(7,9-dichloro-2-cyclopropyl-3,4-dihydro-2h-pyrido[1,2-a]pyrimidin-4-yl)oxy]ethanol Chemical compound N1=C(C(=CC(Cl)=C2)Cl)N2C(OCCO)CC1C1CC1 YAJHBJGCFLKFPH-UHFFFAOYSA-N 0.000 claims description 3
ZHSZDYHNGNXFQD-UHFFFAOYSA-N 2-[[9-chloro-2-cyclohexyl-7-(trifluoromethyl)-3,4-dihydro-2h-pyrido[1,2-a]pyrimidin-4-yl]oxy]ethanol Chemical compound N1=C(C(=CC(=C2)C(F)(F)F)Cl)N2C(OCCO)CC1C1CCCCC1 ZHSZDYHNGNXFQD-UHFFFAOYSA-N 0.000 claims description 3
BWRBHISVOYMLTP-UHFFFAOYSA-N 2-[[9-chloro-2-cyclopropyl-7-(trifluoromethyl)-3,4-dihydro-2h-pyrido[1,2-a]pyrimidin-4-yl]oxy]ethanol Chemical compound N1=C(C(=CC(=C2)C(F)(F)F)Cl)N2C(OCCO)CC1C1CC1 BWRBHISVOYMLTP-UHFFFAOYSA-N 0.000 claims description 3
125000001255 4-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1F 0.000 claims description 3
SXKBKGFZLPVFSZ-UHFFFAOYSA-N 6-chloro-9-nitro-4-phenylsulfanyl-2-pyridin-2-yl-3,4-dihydro-2h-pyrido[1,2-a]pyrimidine Chemical compound N1=C2C([N+](=O)[O-])=CC=C(Cl)N2C(SC=2C=CC=CC=2)CC1C1=CC=CC=N1 SXKBKGFZLPVFSZ-UHFFFAOYSA-N 0.000 claims description 3
JAYGJZIFEPBQMG-UHFFFAOYSA-N 7,9-dibromo-4-(4-hydroxyphenyl)-3,6-dimethyl-3,4-dihydro-2h-pyrido[1,2-a]pyrimidine-2-carboxylic acid Chemical compound CC1C(C(O)=O)N=C(C(=CC(Br)=C2C)Br)N2C1C1=CC=C(O)C=C1 JAYGJZIFEPBQMG-UHFFFAOYSA-N 0.000 claims description 3
RUVVHONEPNHZPE-UHFFFAOYSA-N 7-bromo-4-(4-methoxyphenyl)-3-methyl-9-nitro-3,4-dihydro-2h-pyrido[1,2-a]pyrimidine-2-carboxylic acid Chemical compound C1=CC(OC)=CC=C1C1N(C=C(Br)C=C2[N+]([O-])=O)C2=NC(C(O)=O)C1C RUVVHONEPNHZPE-UHFFFAOYSA-N 0.000 claims description 3
YSJMLWIJKIZYJO-UHFFFAOYSA-N 7-bromo-4-(4-methoxyphenyl)-9-nitro-3,4-dihydro-2h-pyrido[1,2-a]pyrimidine-2-carboxylic acid Chemical compound C1=CC(OC)=CC=C1C1N(C=C(Br)C=C2[N+]([O-])=O)C2=NC(C(O)=O)C1 YSJMLWIJKIZYJO-UHFFFAOYSA-N 0.000 claims description 3
VUIGPPPCOSXZDI-UHFFFAOYSA-N 7-bromo-4-phenylsulfanyl-2-pyridin-2-yl-3,4-dihydro-2h-pyrido[1,2-a]pyrimidine Chemical compound N1=C2C=CC(Br)=CN2C(SC=2C=CC=CC=2)CC1C1=CC=CC=N1 VUIGPPPCOSXZDI-UHFFFAOYSA-N 0.000 claims description 3
CXLHFKUMNVAHTE-UHFFFAOYSA-N 7-bromo-9-methyl-4-phenylsulfanyl-2-pyridin-2-yl-3,4-dihydro-2h-pyrido[1,2-a]pyrimidine Chemical compound N1=C2C(C)=CC(Br)=CN2C(SC=2C=CC=CC=2)CC1C1=CC=CC=N1 CXLHFKUMNVAHTE-UHFFFAOYSA-N 0.000 claims description 3
LFRRVHGUMJKEIU-UHFFFAOYSA-N 7-chloro-10-pyridin-2-yl-5-(trifluoromethyl)-3,9-diazatetracyclo[10.2.1.02,11.03,8]pentadeca-4,6,8,13-tetraene Chemical compound N1=C2C(Cl)=CC(C(F)(F)F)=CN2C2C(C=C3)CC3C2C1C1=CC=CC=N1 LFRRVHGUMJKEIU-UHFFFAOYSA-N 0.000 claims description 3
QOKJNZRGKPCBLV-UHFFFAOYSA-N 7-methyl-4-phenylsulfanyl-2-pyridin-2-yl-3,4-dihydro-2h-pyrido[1,2-a]pyrimidine Chemical compound N1=C2C=CC(C)=CN2C(SC=2C=CC=CC=2)CC1C1=CC=CC=N1 QOKJNZRGKPCBLV-UHFFFAOYSA-N 0.000 claims description 3
CZNHVJIBZSBUAK-UHFFFAOYSA-N 7-nitro-4-phenyl-2-pyridin-2-yl-3,4-dihydro-2h-pyrido[1,2-a]pyrimidine Chemical compound N1=C2C=CC([N+](=O)[O-])=CN2C(C=2C=CC=CC=2)CC1C1=CC=CC=N1 CZNHVJIBZSBUAK-UHFFFAOYSA-N 0.000 claims description 3
GNIDPTAWYKWZQI-UHFFFAOYSA-N 7-nitro-4-phenylsulfanyl-2-pyridin-2-yl-3,4-dihydro-2h-pyrido[1,2-a]pyrimidine Chemical compound N1=C2C=CC([N+](=O)[O-])=CN2C(SC=2C=CC=CC=2)CC1C1=CC=CC=N1 GNIDPTAWYKWZQI-UHFFFAOYSA-N 0.000 claims description 3
FBYFEPLGQWOLCC-UHFFFAOYSA-N 8-methyl-9-nitro-4-phenyl-2-pyridin-2-yl-3,4-dihydro-2h-pyrido[1,2-a]pyrimidine Chemical compound N12C=CC(C)=C([N+]([O-])=O)C2=NC(C=2N=CC=CC=2)CC1C1=CC=CC=C1 FBYFEPLGQWOLCC-UHFFFAOYSA-N 0.000 claims description 3
VYZITDOXZFTCFX-UHFFFAOYSA-N 9-chloro-2-cyclopropyl-4-(3,4-dimethoxyphenyl)-7-(trifluoromethyl)-3,4-dihydro-2h-pyrido[1,2-a]pyrimidine Chemical compound C1=C(OC)C(OC)=CC=C1C1N(C=C(C=C2Cl)C(F)(F)F)C2=NC(C2CC2)C1 VYZITDOXZFTCFX-UHFFFAOYSA-N 0.000 claims description 3
NMALUHKRSBMVSA-UHFFFAOYSA-N 9-chloro-2-cyclopropyl-4-(4-methoxyphenyl)-7-(trifluoromethyl)-3,4-dihydro-2h-pyrido[1,2-a]pyrimidine Chemical compound C1=CC(OC)=CC=C1C1N(C=C(C=C2Cl)C(F)(F)F)C2=NC(C2CC2)C1 NMALUHKRSBMVSA-UHFFFAOYSA-N 0.000 claims description 3
YPQJDDILAJVBQO-UHFFFAOYSA-N 9-chloro-4-(4-hydroxy-3-methoxyphenyl)-3-methyl-7-(trifluoromethyl)-3,4-dihydro-2h-pyrido[1,2-a]pyrimidine-2-carboxylic acid Chemical compound C1=C(O)C(OC)=CC(C2N3C(C(=CC(=C3)C(F)(F)F)Cl)=NC(C2C)C(O)=O)=C1 YPQJDDILAJVBQO-UHFFFAOYSA-N 0.000 claims description 3
WMHARLXIUPPHIB-UHFFFAOYSA-N 9-nitro-4-phenyl-2-pyridin-2-yl-3,4-dihydro-2h-pyrido[1,2-a]pyrimidine Chemical compound N1=C2C([N+](=O)[O-])=CC=CN2C(C=2C=CC=CC=2)CC1C1=CC=CC=N1 WMHARLXIUPPHIB-UHFFFAOYSA-N 0.000 claims description 3
QEBULIIXEURLBQ-UHFFFAOYSA-N 9-nitro-4-phenylsulfanyl-2-pyridin-2-yl-3,4-dihydro-2h-pyrido[1,2-a]pyrimidine Chemical compound N1=C2C([N+](=O)[O-])=CC=CN2C(SC=2C=CC=CC=2)CC1C1=CC=CC=N1 QEBULIIXEURLBQ-UHFFFAOYSA-N 0.000 claims description 3
JHODBOVSMVLPBO-UHFFFAOYSA-N 9-phenylmethoxy-4-phenylsulfanyl-2-pyridin-2-yl-3,4-dihydro-2h-pyrido[1,2-a]pyrimidine Chemical compound C=1C=CC=CC=1COC(C1=N2)=CC=CN1C(SC=1C=CC=CC=1)CC2C1=CC=CC=N1 JHODBOVSMVLPBO-UHFFFAOYSA-N 0.000 claims description 3
RMBPAXFZDGJSGY-UHFFFAOYSA-N C12C(C=C3)CC3C2N2C(C)=C(Br)C=C(Br)C2=NC1C1=CC=CC=N1 Chemical compound C12C(C=C3)CC3C2N2C(C)=C(Br)C=C(Br)C2=NC1C1=CC=CC=N1 RMBPAXFZDGJSGY-UHFFFAOYSA-N 0.000 claims description 3
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 3
XLPHIXVVXUQJLN-UHFFFAOYSA-N [7,9-dibromo-4-(3,4-dimethoxyphenyl)-6-methyl-3,4-dihydro-2h-pyrido[1,2-a]pyrimidin-2-yl]-phenylmethanone Chemical compound C1=C(OC)C(OC)=CC=C1C1N(C(C)=C(Br)C=C2Br)C2=NC(C(=O)C=2C=CC=CC=2)C1 XLPHIXVVXUQJLN-UHFFFAOYSA-N 0.000 claims description 3
KKKWTOSFDQFZFM-UHFFFAOYSA-N [7,9-dibromo-4-(4-hydroxy-3-methoxyphenyl)-3,6-dimethyl-3,4-dihydro-2h-pyrido[1,2-a]pyrimidin-2-yl]-phenylmethanone Chemical compound C1=C(O)C(OC)=CC(C2N3C(C(=CC(Br)=C3C)Br)=NC(C2C)C(=O)C=2C=CC=CC=2)=C1 KKKWTOSFDQFZFM-UHFFFAOYSA-N 0.000 claims description 3
125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims description 3
229940124531 pharmaceutical excipient Drugs 0.000 claims description 3
LEVJVKGPFAQPOI-UHFFFAOYSA-N phenylmethanone Chemical compound O=[C]C1=CC=CC=C1 LEVJVKGPFAQPOI-UHFFFAOYSA-N 0.000 claims description 3
YKGFPMCWTPOCJL-UHFFFAOYSA-N 14-pyridin-2-yl-3,13-diazapentacyclo[14.2.1.02,15.03,12.06,11]nonadeca-4,6,8,10,12,17-hexaene Chemical compound C1C2C=CC1C(N1C(C3=CC=CC=C3C=C1)=N1)C2C1C1=CC=CC=N1 YKGFPMCWTPOCJL-UHFFFAOYSA-N 0.000 claims description 2
DWKFDKWAMLOTML-UHFFFAOYSA-N 2-[(7,9-dibromo-2-cyclohexyl-6-methyl-3,4-dihydro-2h-pyrido[1,2-a]pyrimidin-4-yl)oxy]ethanol Chemical compound C1C(OCCO)N2C(C)=C(Br)C=C(Br)C2=NC1C1CCCCC1 DWKFDKWAMLOTML-UHFFFAOYSA-N 0.000 claims description 2
JSCYCSNLRZJLLZ-UHFFFAOYSA-N 2-[(7,9-dibromo-2-cyclopropyl-3,4-dihydro-2h-pyrido[1,2-a]pyrimidin-4-yl)oxy]ethanol Chemical compound N1=C(C(=CC(Br)=C2)Br)N2C(OCCO)CC1C1CC1 JSCYCSNLRZJLLZ-UHFFFAOYSA-N 0.000 claims description 2
BRSDAUIVOLGTTM-UHFFFAOYSA-N 2-[(7,9-dichloro-2-cyclohexyl-3,4-dihydro-2h-pyrido[1,2-a]pyrimidin-4-yl)oxy]ethanol Chemical compound N1=C(C(=CC(Cl)=C2)Cl)N2C(OCCO)CC1C1CCCCC1 BRSDAUIVOLGTTM-UHFFFAOYSA-N 0.000 claims description 2
BFBYEORFWNYVHE-UHFFFAOYSA-N 2-cyclopropyl-4-(4-methoxyphenyl)-7-nitro-3,4-dihydro-2h-pyrido[1,2-a]pyrimidine Chemical compound C1=CC(OC)=CC=C1C1N2C=C([N+]([O-])=O)C=CC2=NC(C2CC2)C1 BFBYEORFWNYVHE-UHFFFAOYSA-N 0.000 claims description 2
RQUBQOAVAIHHGC-UHFFFAOYSA-N 4-(3,4-dimethoxyphenyl)-7-nitro-2-(5-nitrofuran-2-yl)-3,4-dihydro-2h-pyrido[1,2-a]pyrimidine Chemical compound C1=C(OC)C(OC)=CC=C1C1N2C=C([N+]([O-])=O)C=CC2=NC(C=2OC(=CC=2)[N+]([O-])=O)C1 RQUBQOAVAIHHGC-UHFFFAOYSA-N 0.000 claims description 2
XUJFFANGHSXSBC-UHFFFAOYSA-N 4-(4-methoxyphenyl)-7-nitro-2-(5-nitrofuran-2-yl)-3,4-dihydro-2h-pyrido[1,2-a]pyrimidine Chemical compound C1=CC(OC)=CC=C1C1N2C=C([N+]([O-])=O)C=CC2=NC(C=2OC(=CC=2)[N+]([O-])=O)C1 XUJFFANGHSXSBC-UHFFFAOYSA-N 0.000 claims description 2
MZDULUUPGKALPA-UHFFFAOYSA-N 4-ethoxy-2-phenyl-3,4-dihydro-2h-pyrido[1,2-a]pyrimidine Chemical compound N1=C2C=CC=CN2C(OCC)CC1C1=CC=CC=C1 MZDULUUPGKALPA-UHFFFAOYSA-N 0.000 claims description 2
FXINSEQPXXINKW-UHFFFAOYSA-N 4-phenyl-9-phenylmethoxy-2-pyridin-2-yl-3,4-dihydro-2h-pyrido[1,2-a]pyrimidine Chemical compound C=1C=CC=CC=1COC(C1=N2)=CC=CN1C(C=1C=CC=CC=1)CC2C1=CC=CC=N1 FXINSEQPXXINKW-UHFFFAOYSA-N 0.000 claims description 2
SLLQQSHXHOIIBX-UHFFFAOYSA-N 7,9-dichloro-4-(3,4-dimethoxyphenyl)-2-(5-nitrofuran-2-yl)-3,4-dihydro-2h-pyrido[1,2-a]pyrimidine Chemical compound C1=C(OC)C(OC)=CC=C1C1N(C=C(Cl)C=C2Cl)C2=NC(C=2OC(=CC=2)[N+]([O-])=O)C1 SLLQQSHXHOIIBX-UHFFFAOYSA-N 0.000 claims description 2
FLTDEYBWLKSPRS-UHFFFAOYSA-N 7-bromo-9-nitro-4-phenyl-2-pyridin-2-yl-3,4-dihydro-2h-pyrido[1,2-a]pyrimidine Chemical compound N1=C2C([N+](=O)[O-])=CC(Br)=CN2C(C=2C=CC=CC=2)CC1C1=CC=CC=N1 FLTDEYBWLKSPRS-UHFFFAOYSA-N 0.000 claims description 2
MNZUMECZXYZMIB-UHFFFAOYSA-N 7-chloro-4-phenylsulfanyl-2-pyridin-2-yl-3,4-dihydro-2h-pyrido[1,2-a]pyrimidine Chemical compound N1=C2C=CC(Cl)=CN2C(SC=2C=CC=CC=2)CC1C1=CC=CC=N1 MNZUMECZXYZMIB-UHFFFAOYSA-N 0.000 claims description 2
WNNYMNSKBAROGN-UHFFFAOYSA-N 7-nitro-4-phenylsulfanyl-3,4-dihydro-2h-pyrido[1,2-a]pyrimidine-2-carboxylic acid Chemical compound N12C=C([N+]([O-])=O)C=CC2=NC(C(=O)O)CC1SC1=CC=CC=C1 WNNYMNSKBAROGN-UHFFFAOYSA-N 0.000 claims description 2
HFXRMQZCAIBURX-UHFFFAOYSA-N 7h-pyrano[2,3-d]pyrimidine Chemical compound C1=NC=C2C=CCOC2=N1 HFXRMQZCAIBURX-UHFFFAOYSA-N 0.000 claims description 2
OKSQMGRRQJZPIS-UHFFFAOYSA-N 8-methyl-7-nitro-4-phenylsulfanyl-2-pyridin-2-yl-3,4-dihydro-2h-pyrido[1,2-a]pyrimidine Chemical compound N12C=C([N+]([O-])=O)C(C)=CC2=NC(C=2N=CC=CC=2)CC1SC1=CC=CC=C1 OKSQMGRRQJZPIS-UHFFFAOYSA-N 0.000 claims description 2
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UKRSRHXDYWGJNK-UHFFFAOYSA-N 9-chloro-2-cyclohexyl-4-(4-methoxyphenyl)-7-(trifluoromethyl)-3,4-dihydro-2h-pyrido[1,2-a]pyrimidine Chemical compound C1=CC(OC)=CC=C1C1N(C=C(C=C2Cl)C(F)(F)F)C2=NC(C2CCCCC2)C1 UKRSRHXDYWGJNK-UHFFFAOYSA-N 0.000 claims description 2
HWVWGLAAUHKUCH-UHFFFAOYSA-N [4-(4-methoxyphenyl)-7-nitro-3,4-dihydro-2h-pyrido[1,2-a]pyrimidin-2-yl]-phenylmethanone Chemical compound C1=CC(OC)=CC=C1C1N2C=C([N+]([O-])=O)C=CC2=NC(C(=O)C=2C=CC=CC=2)C1 HWVWGLAAUHKUCH-UHFFFAOYSA-N 0.000 claims description 2
UJECCTJXOSMZCI-UHFFFAOYSA-N [7,9-dibromo-4-(3,4-dimethoxyphenyl)-3,4-dihydro-2h-pyrido[1,2-a]pyrimidin-2-yl]-phenylmethanone Chemical compound C1=C(OC)C(OC)=CC=C1C1N(C=C(Br)C=C2Br)C2=NC(C(=O)C=2C=CC=CC=2)C1 UJECCTJXOSMZCI-UHFFFAOYSA-N 0.000 claims description 2
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LXMTWSOEUWQCCC-UHFFFAOYSA-N 4-phenylsulfanyl-2-pyridin-2-yl-7-(trifluoromethyl)-3,4-dihydro-2h-pyrido[1,2-a]pyrimidine Chemical compound N1=C2C=CC(C(F)(F)F)=CN2C(SC=2C=CC=CC=2)CC1C1=CC=CC=N1 LXMTWSOEUWQCCC-UHFFFAOYSA-N 0.000 claims 1
MTGLIHWIGDRYTQ-UHFFFAOYSA-N 7,9-dichloro-4-(4-hydroxyphenyl)-3-methyl-3,4-dihydro-2h-pyrido[1,2-a]pyrimidine-2-carboxylic acid Chemical compound CC1C(C(O)=O)N=C(C(=CC(Cl)=C2)Cl)N2C1C1=CC=C(O)C=C1 MTGLIHWIGDRYTQ-UHFFFAOYSA-N 0.000 claims 1
FLRXOQZOLDKZQC-UHFFFAOYSA-N C1C2C=CC1C(N1C3=CC=CC=C3C=CC1=N1)C2C1C1=CC=CC=N1 Chemical compound C1C2C=CC1C(N1C3=CC=CC=C3C=CC1=N1)C2C1C1=CC=CC=N1 FLRXOQZOLDKZQC-UHFFFAOYSA-N 0.000 claims 1
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239000011787 zinc oxide Substances 0.000 description 1
XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 description 1
NWONKYPBYAMBJT-UHFFFAOYSA-L zinc sulfate Chemical compound [Zn+2].[O-]S([O-])(=O)=O NWONKYPBYAMBJT-UHFFFAOYSA-L 0.000 description 1
229910000368 zinc sulfate Inorganic materials 0.000 description 1
229960001763 zinc sulfate Drugs 0.000 description 1
108020001612 μ-opioid receptors Proteins 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- 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
- C07D471/04—Ortho-condensed systems
- 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
- A61P1/12—Antidiarrhoeals
- 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
- 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
- A61P17/04—Antipruritics
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/04—Centrally acting analgesics, e.g. opioids
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/16—Otologicals
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]

Landscapes

Health & Medical Sciences (AREA)
Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Veterinary Medicine (AREA)
Life Sciences & Earth Sciences (AREA)
Public Health (AREA)
General Health & Medical Sciences (AREA)
Animal Behavior & Ethology (AREA)
Chemical Kinetics & Catalysis (AREA)
General Chemical & Material Sciences (AREA)
Medicinal Chemistry (AREA)
Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
Pharmacology & Pharmacy (AREA)
Engineering & Computer Science (AREA)
Bioinformatics & Cheminformatics (AREA)
Pain & Pain Management (AREA)
Biomedical Technology (AREA)
Neurosurgery (AREA)
Neurology (AREA)
Rheumatology (AREA)
Urology & Nephrology (AREA)
Dermatology (AREA)
Nitrogen Condensed Heterocyclic Rings (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

SK414-2003A 2000-10-13 2001-10-10 Substituted 3,4-dihydro-pyrido[1,2-A]pyrimidines, process for producing thereof, medicaments comprising same and their use SK4142003A3 (en)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
DE10050662A DE10050662A1 (de)	2000-10-13	2000-10-13	Substituierte 3,4-Dihydro-pyrido[1,2-a]pyrimidine
PCT/EP2001/011700 WO2002030933A1 (de)	2000-10-13	2001-10-10	Substituierte 3,4-dihydro-pyrido[1,2-a]pyrimidine

Publications (1)

Publication Number	Publication Date
SK4142003A3 true SK4142003A3 (en)	2003-10-07

Family

ID=7659597

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
SK414-2003A SK4142003A3 (en)	2000-10-13	2001-10-10	Substituted 3,4-dihydro-pyrido[1,2-A]pyrimidines, process for producing thereof, medicaments comprising same and their use

Country Status (26)

Country	Link
US (1)	US7230103B2 (es)
EP (1)	EP1326866B1 (es)
JP (1)	JP4315678B2 (es)
KR (1)	KR20030036924A (es)
CN (1)	CN1255407C (es)
AR (1)	AR034266A1 (es)
AT (1)	ATE297927T1 (es)
AU (2)	AU2002210526B2 (es)
BR (1)	BR0114734A (es)
CA (1)	CA2425666A1 (es)
CO (1)	CO5640115A2 (es)
DE (2)	DE10050662A1 (es)
EC (1)	ECSP034553A (es)
ES (1)	ES2241882T3 (es)
HU (1)	HUP0302464A2 (es)
IL (2)	IL155380A0 (es)
MX (1)	MXPA03003198A (es)
NO (1)	NO20031412L (es)
NZ (1)	NZ525652A (es)
PE (1)	PE20020435A1 (es)
PL (1)	PL361915A1 (es)
PT (1)	PT1326866E (es)
RU (1)	RU2003113966A (es)
SK (1)	SK4142003A3 (es)
WO (1)	WO2002030933A1 (es)
ZA (1)	ZA200303640B (es)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE10310106A1 (de)	2003-03-06	2004-09-16	Grünenthal GmbH	Substituierte Pyridot [1,2-a]pyrimidin-Verbindungen
RU2269538C1 (ru) *	2004-12-30	2006-02-10	Общество с ограниченной ответственностью "Исследовательский Институт Химического Разнообразия" (ООО "Исследовательский Институт Химического Разнообразия")	ЗАМЕЩЕННЫЕ ПИРИДО[4',3':5,6]ПИРАНО[2,3-d]ПИРИМИДИНЫ И КОМБИНАТОРНАЯ БИБЛИОТЕКА
US20070155738A1 (en)	2005-05-20	2007-07-05	Alantos Pharmaceuticals, Inc.	Heterobicyclic metalloprotease inhibitors
EP2379566A2 (en) *	2008-12-22	2011-10-26	Schering Corporation	Gamma secretase modulators

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
HU178910B (en) *	1977-08-19	1982-07-28	Chinoin Gyogyszer Es Vegyeszet	Process for preparing 2,3-disubstituted-4-oxo-4h-pyrido/1,2-a/-pyrimidines
US4666912A (en) *	1984-11-12	1987-05-19	Chinoin Gyogyszer Es Vegyeszeti Termeker Gyara Rt	Treating process

2000
- 2000-10-13 DE DE10050662A patent/DE10050662A1/de not_active Withdrawn
2001
- 2001-10-09 AR ARP010104731A patent/AR034266A1/es unknown
- 2001-10-10 RU RU2003113966/04A patent/RU2003113966A/ru not_active Application Discontinuation
- 2001-10-10 AU AU2002210526A patent/AU2002210526B2/en not_active Ceased
- 2001-10-10 BR BR0114734-0A patent/BR0114734A/pt not_active Application Discontinuation
- 2001-10-10 NZ NZ525652A patent/NZ525652A/en unknown
- 2001-10-10 ES ES01978402T patent/ES2241882T3/es not_active Expired - Lifetime
- 2001-10-10 KR KR10-2003-7005162A patent/KR20030036924A/ko not_active Withdrawn
- 2001-10-10 PT PT01978402T patent/PT1326866E/pt unknown
- 2001-10-10 WO PCT/EP2001/011700 patent/WO2002030933A1/de not_active Ceased
- 2001-10-10 AU AU1052602A patent/AU1052602A/xx active Pending
- 2001-10-10 AT AT01978402T patent/ATE297927T1/de active
- 2001-10-10 EP EP01978402A patent/EP1326866B1/de not_active Expired - Lifetime
- 2001-10-10 CN CNB018205011A patent/CN1255407C/zh not_active Expired - Fee Related
- 2001-10-10 MX MXPA03003198A patent/MXPA03003198A/es active IP Right Grant
- 2001-10-10 HU HU0302464A patent/HUP0302464A2/hu unknown
- 2001-10-10 JP JP2002534319A patent/JP4315678B2/ja not_active Expired - Fee Related
- 2001-10-10 PL PL01361915A patent/PL361915A1/xx not_active Application Discontinuation
- 2001-10-10 IL IL15538001A patent/IL155380A0/xx active IP Right Grant
- 2001-10-10 DE DE50106542T patent/DE50106542D1/de not_active Expired - Lifetime
- 2001-10-10 CA CA002425666A patent/CA2425666A1/en not_active Abandoned
- 2001-10-10 SK SK414-2003A patent/SK4142003A3/sk not_active Application Discontinuation
- 2001-10-12 PE PE2001001014A patent/PE20020435A1/es not_active Application Discontinuation
2003
- 2003-03-27 NO NO20031412A patent/NO20031412L/no not_active Application Discontinuation
- 2003-04-10 IL IL155380A patent/IL155380A/en not_active IP Right Cessation
- 2003-04-11 US US10/411,390 patent/US7230103B2/en not_active Expired - Fee Related
- 2003-04-11 CO CO03031095A patent/CO5640115A2/es not_active Application Discontinuation
- 2003-04-11 EC EC2003004553A patent/ECSP034553A/es unknown
- 2003-05-12 ZA ZA200303640A patent/ZA200303640B/en unknown

Also Published As

Publication number	Publication date
ATE297927T1 (de)	2005-07-15
CA2425666A1 (en)	2003-04-11
US7230103B2 (en)	2007-06-12
JP2004511484A (ja)	2004-04-15
NO20031412D0 (no)	2003-03-27
NZ525652A (en)	2005-01-28
CN1479740A (zh)	2004-03-03
HUP0302464A2 (hu)	2003-11-28
CN1255407C (zh)	2006-05-10
JP4315678B2 (ja)	2009-08-19
RU2003113966A (ru)	2004-12-10
WO2002030933A1 (de)	2002-04-18
US20030229104A1 (en)	2003-12-11
PE20020435A1 (es)	2002-05-18
AR034266A1 (es)	2004-02-18
EP1326866B1 (de)	2005-06-15
DE10050662A1 (de)	2002-04-18
ES2241882T3 (es)	2005-11-01
KR20030036924A (ko)	2003-05-09
BR0114734A (pt)	2003-07-01
AU2002210526B2 (en)	2006-10-19
EP1326866A1 (de)	2003-07-16
PL361915A1 (en)	2004-10-04
PT1326866E (pt)	2005-08-31
ECSP034553A (es)	2003-05-26
IL155380A0 (en)	2003-11-23
IL155380A (en)	2009-02-11
AU1052602A (en)	2002-04-22
CO5640115A2 (es)	2006-05-31
DE50106542D1 (de)	2005-07-21
MXPA03003198A (es)	2004-05-21
NO20031412L (no)	2003-04-22
HK1057551A1 (en)	2004-04-08
ZA200303640B (en)	2004-08-12

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MXPA98000411A (es)	1998-04-01	Compuestos quimicos
WO2007117180A1 (fr)	2007-10-18	Bibliothèques combinatoire et focalisée d'azahétérocycles, composition pharmaceutique et procédés de leur fabrication
SK11542003A3 (sk)	2004-07-07	Substituované pyrazolopyrimidíny a tiazolopyrimidíny, spôsob ich výroby, liečivá tieto látky obsahujúce a ich použitie
CA2771432A1 (en)	2011-02-24	Heterocyclic oxime compounds
JP2009535295A (ja)	2009-10-01	キナーゼ阻害剤として有用なピロロトリアジンアニリンプロドラッグ化合物
JP4559851B2 (ja)	2010-10-13	フェニルアミノピリミジンおよびＲｈｏ−キナーゼ阻害剤としてのその使用
WO2009154870A1 (en)	2009-12-23	Hiv integrase inhibitors
WO2002060907A1 (en)	2002-08-08	Heterocyclic compounds and cerebral function improvers containing the same as the active ingredient
SK4142003A3 (en)	2003-10-07	Substituted 3,4-dihydro-pyrido[1,2-A]pyrimidines, process for producing thereof, medicaments comprising same and their use
SK4152003A3 (en)	2003-10-07	Substituted 3,4-dihydro-pyrimido[1,2-a]pyrimidines and 3,4-dihydropyrazino[1,2-a]pyrimidines, process for producing thereof, medicaments comprising same and their use
TW202434582A (zh)	2024-09-01	Ｓｏｓ１抑制劑
ES2281251A1 (es)	2007-09-16	Nuevos derivados de pirido (3',2',4',5) furo (3,2-d) pirimidina.
TW202246261A (zh)	2022-12-01	作為抗癌劑的化合物

Legal Events

Date	Code	Title	Description
2012-04-03	FC9A	Refused patent application