SK11542003A3 - Substituované pyrazolopyrimidíny a tiazolopyrimidíny, spôsob ich výroby, liečivá tieto látky obsahujúce a ich použitie - Google Patents

Substituované pyrazolopyrimidíny a tiazolopyrimidíny, spôsob ich výroby, liečivá tieto látky obsahujúce a ich použitie Download PDF

Info

Publication number: SK11542003A3
Authority: SK; Slovakia
Prior art keywords: group; carbon atoms; cycloalkyl; alkyl; phenyl
Prior art date: 2001-03-14

Application number

SK1154-2003A

Other languages

English (en)

Slovak (sk)

Inventor

Matthias Gerlach

Corinna Maul

Utz-Peter Jagusch

Bernd Sundermann

Martin Fuhr

Adriaan P. Ijzerman

Groote Miriam Dissen-De

Original Assignee

Grnenthal Gmbh

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.)

2001-03-14

Filing date

2002-03-13

Publication date

2004-07-07

2001-03-14 Priority claimed from DE2001112197 external-priority patent/DE10112197A1/de

2001-10-29 Priority claimed from DE2001153344 external-priority patent/DE10153344A1/de

2002-03-13 Application filed by Grnenthal Gmbh filed Critical Grnenthal Gmbh

2004-07-07 Publication of SK11542003A3 publication Critical patent/SK11542003A3/sk

Links

APXRHPDHORGIEB-UHFFFAOYSA-N 1H-pyrazolo[4,3-d]pyrimidine Chemical class N1=CN=C2C=NNC2=C1 APXRHPDHORGIEB-UHFFFAOYSA-N 0.000 title claims description 12
150000008634 thiazolopyrimidines Chemical class 0.000 title claims description 11
229940035676 analgesics Drugs 0.000 title 1
239000000730 antalgic agent Substances 0.000 title 1
125000000217 alkyl group Chemical group 0.000 claims abstract description 275
-1 thiazolo-pyrimidine compounds Chemical class 0.000 claims abstract description 258
125000003118 aryl group Chemical group 0.000 claims abstract description 224
125000000753 cycloalkyl group Chemical group 0.000 claims abstract description 156
150000001875 compounds Chemical class 0.000 claims abstract description 113
125000000623 heterocyclic group Chemical group 0.000 claims abstract description 47
150000003839 salts Chemical class 0.000 claims abstract description 46
239000000203 mixture Substances 0.000 claims abstract description 31
239000002253 acid Substances 0.000 claims abstract description 26
239000003814 drug Substances 0.000 claims abstract description 26
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 abstract description 24
239000003446 ligand Substances 0.000 claims abstract description 12
229910052760 oxygen Inorganic materials 0.000 claims abstract description 12
150000004677 hydrates Chemical class 0.000 claims abstract description 11
239000012453 solvate Substances 0.000 claims abstract description 11
229910052717 sulfur Inorganic materials 0.000 claims abstract description 11
238000002360 preparation method Methods 0.000 claims abstract description 10
102000055025 Adenosine deaminases Human genes 0.000 claims abstract description 6
102100032534 Adenosine kinase Human genes 0.000 claims abstract description 6
108010076278 Adenosine kinase Proteins 0.000 claims abstract description 6
102000019055 Nucleoside Transport Proteins Human genes 0.000 claims abstract description 6
108010012315 Nucleoside Transport Proteins Proteins 0.000 claims abstract description 6
101710169336 5'-deoxyadenosine deaminase Proteins 0.000 claims abstract description 4
OOXNYFKPOPJIOT-UHFFFAOYSA-N 5-(3-bromophenyl)-7-(6-morpholin-4-ylpyridin-3-yl)pyrido[2,3-d]pyrimidin-4-amine;dihydrochloride Chemical compound Cl.Cl.C=12C(N)=NC=NC2=NC(C=2C=NC(=CC=2)N2CCOCC2)=CC=1C1=CC=CC(Br)=C1 OOXNYFKPOPJIOT-UHFFFAOYSA-N 0.000 claims abstract description 4
AMBPCUJCEYOPTB-UHFFFAOYSA-N 2-(4-nitrophenyl)-4-phenyl-3,4-dihydro-2h-pyrimido[2,1-b][1,3]benzothiazole Chemical compound C1=CC([N+](=O)[O-])=CC=C1C1N=C(SC=2C3=CC=CC=2)N3C(C=2C=CC=CC=2)C1 AMBPCUJCEYOPTB-UHFFFAOYSA-N 0.000 claims abstract description 3
CJPCIJLKUZKGER-UHFFFAOYSA-N 4-(4-methylphenyl)-2-(4-nitrophenyl)-3,4-dihydro-2h-pyrimido[2,1-b][1,3]benzothiazole Chemical compound C1=CC(C)=CC=C1C1N2C3=CC=CC=C3SC2=NC(C=2C=CC(=CC=2)[N+]([O-])=O)C1 CJPCIJLKUZKGER-UHFFFAOYSA-N 0.000 claims abstract description 3
125000004432 carbon atom Chemical group C* 0.000 claims description 412
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 202
229910052739 hydrogen Inorganic materials 0.000 claims description 103
239000001257 hydrogen Substances 0.000 claims description 103
150000003254 radicals Chemical class 0.000 claims description 86
125000002877 alkyl aryl group Chemical group 0.000 claims description 74
125000002496 methyl group Chemical class [H]C([H])([H])* 0.000 claims description 59
125000001495 ethyl group Chemical class [H]C([H])([H])C([H])([H])* 0.000 claims description 57
125000004429 atom Chemical group 0.000 claims description 49
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical compound BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 42
125000000999 tert-butyl group Chemical class [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 40
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 35
125000004108 n-butyl group Chemical class [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 33
229910052801 chlorine Inorganic materials 0.000 claims description 32
229910052731 fluorine Inorganic materials 0.000 claims description 32
125000004494 ethyl ester group Chemical group 0.000 claims description 31
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 30
125000004123 n-propyl group Chemical class [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 30
239000000460 chlorine Substances 0.000 claims description 29
125000001449 isopropyl group Chemical class [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 29
229910052794 bromium Inorganic materials 0.000 claims description 28
239000011737 fluorine Substances 0.000 claims description 26
125000004172 4-methoxyphenyl group Chemical group [H]C1=C([H])C(OC([H])([H])[H])=C([H])C([H])=C1* 0.000 claims description 25
PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 25
125000000959 isobutyl group Chemical class [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims description 25
238000000034 method Methods 0.000 claims description 25
125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 claims description 25
125000002914 sec-butyl group Chemical class [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 25
125000004093 cyano group Chemical group *C#N 0.000 claims description 24
229910052740 iodine Inorganic materials 0.000 claims description 23
125000004528 pyrimidin-5-yl group Chemical group N1=CN=CC(=C1)* 0.000 claims description 22
ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical group [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims description 21
125000001972 isopentyl group Chemical class [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 claims description 21
125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims description 20
125000004491 isohexyl group Chemical class C(CCC(C)C)* 0.000 claims description 20
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 19
125000004203 4-hydroxyphenyl group Chemical group [H]OC1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 17
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 17
238000011282 treatment Methods 0.000 claims description 17
KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 claims description 16
208000002193 Pain Diseases 0.000 claims description 16
150000007513 acids Chemical class 0.000 claims description 16
150000001336 alkenes Chemical class 0.000 claims description 16
125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 claims description 16
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 claims description 15
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 15
125000003277 amino group Chemical group 0.000 claims description 15
125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims description 15
JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 claims description 15
238000004519 manufacturing process Methods 0.000 claims description 14
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 13
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 13
230000036407 pain Effects 0.000 claims description 13
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 13
DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 claims description 12
125000005119 alkyl cycloalkyl group Chemical group 0.000 claims description 12
125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 12
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 12
206010021143 Hypoxia Diseases 0.000 claims description 11
238000006243 chemical reaction Methods 0.000 claims description 11
CSOYDALHEQEMAK-UHFFFAOYSA-N 2h-pyrimidine-1-carboxylic acid Chemical compound OC(=O)N1CN=CC=C1 CSOYDALHEQEMAK-UHFFFAOYSA-N 0.000 claims description 10
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical group [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 10
125000001153 fluoro group Chemical group F* 0.000 claims description 10
125000001424 substituent group Chemical group 0.000 claims description 10
125000006275 3-bromophenyl group Chemical group [H]C1=C([H])C(Br)=C([H])C(*)=C1[H] 0.000 claims description 9
SXIFAEWFOJETOA-UHFFFAOYSA-N 4-hydroxy-butyl Chemical group [CH2]CCCO SXIFAEWFOJETOA-UHFFFAOYSA-N 0.000 claims description 9
125000001309 chloro group Chemical group Cl* 0.000 claims description 9
125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims description 9
201000010099 disease Diseases 0.000 claims description 9
208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 9
125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 9
230000004770 neurodegeneration Effects 0.000 claims description 9
208000015122 neurodegenerative disease Diseases 0.000 claims description 9
201000000980 schizophrenia Diseases 0.000 claims description 9
BFKYQYMHJANOTR-UHFFFAOYSA-N 2h-pyrimidine-1-carbonitrile Chemical compound N#CN1CN=CC=C1 BFKYQYMHJANOTR-UHFFFAOYSA-N 0.000 claims description 8
206010008118 cerebral infarction Diseases 0.000 claims description 8
206010015037 epilepsy Diseases 0.000 claims description 8
229960004889 salicylic acid Drugs 0.000 claims description 8
125000004105 2-pyridyl group Chemical group N1=C([*])C([H])=C([H])C([H])=C1[H] 0.000 claims description 7
125000003349 3-pyridyl group Chemical group N1=C([H])C([*])=C([H])C([H])=C1[H] 0.000 claims description 7
125000001246 bromo group Chemical group Br* 0.000 claims description 7
229910052799 carbon Inorganic materials 0.000 claims description 7
RAIPHJJURHTUIC-UHFFFAOYSA-N 1,3-thiazol-2-amine Chemical compound NC1=NC=CS1 RAIPHJJURHTUIC-UHFFFAOYSA-N 0.000 claims description 6
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 6
125000004180 3-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(F)=C1[H] 0.000 claims description 6
241000976983 Anoxia Species 0.000 claims description 6
206010048962 Brain oedema Diseases 0.000 claims description 6
208000023105 Huntington disease Diseases 0.000 claims description 6
208000018737 Parkinson disease Diseases 0.000 claims description 6
150000001413 amino acids Chemical class 0.000 claims description 6
230000007953 anoxia Effects 0.000 claims description 6
210000003169 central nervous system Anatomy 0.000 claims description 6
201000002491 encephalomyelitis Diseases 0.000 claims description 6
229960001867 guaiacol Drugs 0.000 claims description 6
230000007954 hypoxia Effects 0.000 claims description 6
208000026278 immune system disease Diseases 0.000 claims description 6
230000002265 prevention Effects 0.000 claims description 6
125000004800 4-bromophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Br 0.000 claims description 5
125000001255 4-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1F 0.000 claims description 5
208000030507 AIDS Diseases 0.000 claims description 5
206010002660 Anoxia Diseases 0.000 claims description 5
206010008120 Cerebral ischaemia Diseases 0.000 claims description 5
206010012289 Dementia Diseases 0.000 claims description 5
201000004311 Gilles de la Tourette syndrome Diseases 0.000 claims description 5
206010028923 Neonatal asphyxia Diseases 0.000 claims description 5
208000037212 Neonatal hypoxic and ischemic brain injury Diseases 0.000 claims description 5
208000028017 Psychotic disease Diseases 0.000 claims description 5
208000009205 Tinnitus Diseases 0.000 claims description 5
208000000323 Tourette Syndrome Diseases 0.000 claims description 5
208000016620 Tourette disease Diseases 0.000 claims description 5
125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims description 5
125000000582 cycloheptyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 5
125000002485 formyl group Chemical class [H]C(*)=O 0.000 claims description 5
125000002541 furyl group Chemical group 0.000 claims description 5
239000011630 iodine Chemical group 0.000 claims description 5
208000033300 perinatal asphyxia Diseases 0.000 claims description 5
239000008194 pharmaceutical composition Substances 0.000 claims description 5
239000000546 pharmaceutical excipient Substances 0.000 claims description 5
238000011321 prophylaxis Methods 0.000 claims description 5
125000004076 pyridyl group Chemical group 0.000 claims description 5
VTGOHKSTWXHQJK-UHFFFAOYSA-N pyrimidin-2-ol Chemical compound OC1=NC=CC=N1 VTGOHKSTWXHQJK-UHFFFAOYSA-N 0.000 claims description 5
125000001544 thienyl group Chemical group 0.000 claims description 5
231100000886 tinnitus Toxicity 0.000 claims description 5
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 5
125000002941 2-furyl group Chemical group O1C([*])=C([H])C([H])=C1[H] 0.000 claims description 4
125000000175 2-thienyl group Chemical group S1C([*])=C([H])C([H])=C1[H] 0.000 claims description 4
ZJHKPJQQFNNZEL-UHFFFAOYSA-N 3-cyano-2-methylsulfanyl-7-(2,3,4-trimethoxyphenyl)-1,2,3,3a-tetrahydropyrazolo[1,5-a]pyrimidine-5-carboxylic acid Chemical compound COC1=C(OC)C(OC)=CC=C1C1=CC(C(O)=O)=NC2N1NC(SC)C2C#N ZJHKPJQQFNNZEL-UHFFFAOYSA-N 0.000 claims description 4
XTSMYJXQALSHRE-UHFFFAOYSA-N 3-cyano-7-(2,4-dimethylphenyl)-1,2,3,3a-tetrahydropyrazolo[1,5-a]pyrimidine-5-carboxylic acid Chemical compound CC1=CC(C)=CC=C1C1=CC(C(O)=O)=NC2N1NCC2C#N XTSMYJXQALSHRE-UHFFFAOYSA-N 0.000 claims description 4
125000003682 3-furyl group Chemical group O1C([H])=C([*])C([H])=C1[H] 0.000 claims description 4
125000001541 3-thienyl group Chemical group S1C([H])=C([*])C([H])=C1[H] 0.000 claims description 4
125000000339 4-pyridyl group Chemical group N1=C([H])C([H])=C([*])C([H])=C1[H] 0.000 claims description 4
QOKLSVOEHNDZCY-UHFFFAOYSA-N 9h-fluorene-3-carbonitrile Chemical compound C1=CC=C2C3=CC(C#N)=CC=C3CC2=C1 QOKLSVOEHNDZCY-UHFFFAOYSA-N 0.000 claims description 4
208000024827 Alzheimer disease Diseases 0.000 claims description 4
206010028980 Neoplasm Diseases 0.000 claims description 4
208000007536 Thrombosis Diseases 0.000 claims description 4
201000011510 cancer Diseases 0.000 claims description 4
150000002148 esters Chemical class 0.000 claims description 4
230000007574 infarction Effects 0.000 claims description 4
125000002346 iodo group Chemical group I* 0.000 claims description 4
125000000040 m-tolyl group Chemical group [H]C1=C([H])C(*)=C([H])C(=C1[H])C([H])([H])[H] 0.000 claims description 4
125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 4
208000004296 neuralgia Diseases 0.000 claims description 4
208000021722 neuropathic pain Diseases 0.000 claims description 4
125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 3
FYFQRPMJHBIASN-UHFFFAOYSA-N 2,5-ditert-butyl-7-(3,4-dimethoxyphenyl)-1,2,3,3a-tetrahydropyrazolo[1,5-a]pyrimidine Chemical compound C1=C(OC)C(OC)=CC=C1C1=CC(C(C)(C)C)=NC2N1NC(C(C)(C)C)C2 FYFQRPMJHBIASN-UHFFFAOYSA-N 0.000 claims description 3
GDMMHFDAAJPEGF-UHFFFAOYSA-N 2-[(2-tert-butyl-5-cyclopropyl-1,2,3,3a-tetrahydropyrazolo[1,5-a]pyrimidin-7-yl)oxy]ethanol Chemical compound C1=C(OCCO)N2NC(C(C)(C)C)CC2N=C1C1CC1 GDMMHFDAAJPEGF-UHFFFAOYSA-N 0.000 claims description 3
DVPKGHMXKJSIBR-UHFFFAOYSA-N 3-(3-cyano-7-phenylsulfanyl-1,2,3,3a-tetrahydropyrazolo[1,5-a]pyrimidin-5-yl)-2-hydroxybenzoic acid Chemical compound C(#N)C1CNN2C1N=C(C=C2SC2=CC=CC=C2)C=2C(=C(C(=O)O)C=CC2)O DVPKGHMXKJSIBR-UHFFFAOYSA-N 0.000 claims description 3
QKHJTJNKWGXNID-UHFFFAOYSA-N 3-(4-methylphenyl)-5-phenylsulfanyl-7-pyridin-2-yl-6,7-dihydro-5h-[1,3]thiazolo[3,2-a]pyrimidine Chemical compound C1=CC(C)=CC=C1C(N12)=CSC2=NC(C=2N=CC=CC=2)CC1SC1=CC=CC=C1 QKHJTJNKWGXNID-UHFFFAOYSA-N 0.000 claims description 3
FNANXDCOTZQWMD-UHFFFAOYSA-N 3-bromo-7-(2,4-dimethylphenyl)-2-phenyl-1,2,3,3a-tetrahydropyrazolo[1,5-a]pyrimidine-5-carboxylic acid Chemical compound CC1=CC(C)=CC=C1C1=CC(C(O)=O)=NC2N1NC(C=1C=CC=CC=1)C2Br FNANXDCOTZQWMD-UHFFFAOYSA-N 0.000 claims description 3
GQCOXXJMGFBZCB-UHFFFAOYSA-N 3-bromo-7-(2,4-dimethylphenyl)-5-(4-phenoxyphenyl)-2-phenyl-1,2,3,3a-tetrahydropyrazolo[1,5-a]pyrimidine Chemical compound CC1=CC(C)=CC=C1C1=CC(C=2C=CC(OC=3C=CC=CC=3)=CC=2)=NC2N1NC(C=1C=CC=CC=1)C2Br GQCOXXJMGFBZCB-UHFFFAOYSA-N 0.000 claims description 3
ZERXYYVJVUIUNU-UHFFFAOYSA-N 3-bromo-7-(2,4-dimethylphenyl)-5-(5-nitrofuran-2-yl)-2-phenyl-1,2,3,3a-tetrahydropyrazolo[1,5-a]pyrimidine Chemical compound CC1=CC(C)=CC=C1C1=CC(C=2OC(=CC=2)[N+]([O-])=O)=NC2N1NC(C=1C=CC=CC=1)C2Br ZERXYYVJVUIUNU-UHFFFAOYSA-N 0.000 claims description 3
SIWXPIMGOSUHTA-UHFFFAOYSA-N 3-bromo-7-(4-methoxyphenyl)-1,2,3,3a-tetrahydropyrazolo[1,5-a]pyrimidine-5-carboxylic acid Chemical compound C1=CC(OC)=CC=C1C1=CC(C(O)=O)=NC2N1NCC2Br SIWXPIMGOSUHTA-UHFFFAOYSA-N 0.000 claims description 3
OASJNZSHIIPOGP-UHFFFAOYSA-N 3-bromo-7-phenylsulfanyl-5-pyridin-2-yl-3,5,6,7-tetrahydropyrazolo[1,5-a]pyrimidine Chemical compound N1=C2C(Br)C=NN2C(SC=2C=CC=CC=2)CC1C1=CC=CC=N1 OASJNZSHIIPOGP-UHFFFAOYSA-N 0.000 claims description 3
WQVYBOYDOARVCM-UHFFFAOYSA-N 3-naphthalen-2-yl-5-phenylsulfanyl-7-pyridin-2-yl-6,7-dihydro-5h-[1,3]thiazolo[3,2-a]pyrimidine Chemical compound S1C=C(C=2C=C3C=CC=CC3=CC=2)N2C1=NC(C=1N=CC=CC=1)CC2SC1=CC=CC=C1 WQVYBOYDOARVCM-UHFFFAOYSA-N 0.000 claims description 3
VLPRLOVNQLRKCM-UHFFFAOYSA-N 5-(4-hydroxybutyl)-7-phenylsulfanyl-1,2,3,3a-tetrahydropyrazolo[1,5-a]pyrimidine-3-carbonitrile Chemical compound C=1C(CCCCO)=NC2C(C#N)CNN2C=1SC1=CC=CC=C1 VLPRLOVNQLRKCM-UHFFFAOYSA-N 0.000 claims description 3
HNFXTBAUEBGHMJ-UHFFFAOYSA-N 5-butyl-2-methylsulfanyl-7-phenylsulfanyl-1,2,3,3a-tetrahydropyrazolo[1,5-a]pyrimidine-3-carbonitrile Chemical compound C=1C(CCCC)=NC2C(C#N)C(SC)NN2C=1SC1=CC=CC=C1 HNFXTBAUEBGHMJ-UHFFFAOYSA-N 0.000 claims description 3
IAHBZYBBYSTUOV-UHFFFAOYSA-N 5-butyl-7-phenylsulfanyl-1,2,3,3a-tetrahydropyrazolo[1,5-a]pyrimidine-3-carbonitrile Chemical compound C=1C(CCCC)=NC2C(C#N)CNN2C=1SC1=CC=CC=C1 IAHBZYBBYSTUOV-UHFFFAOYSA-N 0.000 claims description 3
KUBGUWWVTSJFSQ-UHFFFAOYSA-N 7-(2,4-dimethylphenyl)-2-methylsulfanyl-5-(4-phenoxyphenyl)-1,2,3,3a-tetrahydropyrazolo[1,5-a]pyrimidine-3-carbonitrile Chemical compound N#CC1C(SC)NN2C1N=C(C=1C=CC(OC=3C=CC=CC=3)=CC=1)C=C2C1=CC=C(C)C=C1C KUBGUWWVTSJFSQ-UHFFFAOYSA-N 0.000 claims description 3
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VGONTNSXDCQUGY-UHFFFAOYSA-N desoxyinosine Natural products C1C(O)C(CO)OC1N1C(NC=NC2=O)=C2N=C1 VGONTNSXDCQUGY-UHFFFAOYSA-N 0.000 description 1
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CDAXUULONNMABU-UHFFFAOYSA-N diethyl 2H-pyrimidine-1,5-dicarboxylate Chemical compound CCOC(=O)N1CN=CC(=C1)C(=O)OCC CDAXUULONNMABU-UHFFFAOYSA-N 0.000 description 1
GVXIGYMWZUEEMI-UHFFFAOYSA-N diethyl 7-(2,3,4-trimethoxyphenyl)-1,2,3,3a-tetrahydropyrazolo[1,5-a]pyrimidine-3,5-dicarboxylate Chemical compound CCOC(=O)C1CNN2C1N=C(C(=O)OCC)C=C2C1=CC=C(OC)C(OC)=C1OC GVXIGYMWZUEEMI-UHFFFAOYSA-N 0.000 description 1
RFWWOHKMHRVFDD-UHFFFAOYSA-N diethyl 9H-fluorene-3,5-dicarboxylate Chemical compound C(C)OC(=O)C=1C=CC=2CC=3C=CC=C(C=3C=2C=1)C(=O)OCC RFWWOHKMHRVFDD-UHFFFAOYSA-N 0.000 description 1
239000003085 diluting agent Substances 0.000 description 1
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MOBLKXVCSMSERI-UHFFFAOYSA-N ethyl 2-[3-bromo-7-(3-bromophenyl)-2-phenyl-1,2,3,3a-tetrahydropyrazolo[1,5-a]pyrimidin-5-yl]cyclopropane-1-carboxylate Chemical compound CCOC(=O)C1CC1C(C=C1C=2C=C(Br)C=CC=2)=NC2N1NC(C=1C=CC=CC=1)C2Br MOBLKXVCSMSERI-UHFFFAOYSA-N 0.000 description 1
VPWKGRJDOXBEQP-UHFFFAOYSA-N ethyl 2-[3-bromo-7-(3-methylphenyl)-1,2,3,3a-tetrahydropyrazolo[1,5-a]pyrimidin-5-yl]cyclopropane-1-carboxylate Chemical compound CCOC(=O)C1CC1C(C=C1C=2C=C(C)C=CC=2)=NC2N1NCC2Br VPWKGRJDOXBEQP-UHFFFAOYSA-N 0.000 description 1
QJQHNMWDPOCCKD-UHFFFAOYSA-N ethyl 2-[7-(2,4-dimethylphenyl)-2-hydroxy-3-phenyldiazenyl-1,2,3,3a-tetrahydropyrazolo[1,5-a]pyrimidin-5-yl]cyclopropane-1-carboxylate Chemical compound CCOC(=O)C1CC1C(C=C1C=2C(=CC(C)=CC=2)C)=NC2N1NC(O)C2N=NC1=CC=CC=C1 QJQHNMWDPOCCKD-UHFFFAOYSA-N 0.000 description 1
PRNZPLBZGJVWKJ-UHFFFAOYSA-N ethyl 2-[7-(3-bromophenyl)-3-cyano-2-methylsulfanyl-1,2,3,3a-tetrahydropyrazolo[1,5-a]pyrimidin-5-yl]cyclopropane-1-carboxylate Chemical compound CCOC(=O)C1CC1C(C=C1C=2C=C(Br)C=CC=2)=NC2N1NC(SC)C2C#N PRNZPLBZGJVWKJ-UHFFFAOYSA-N 0.000 description 1
XHUWDDXMORFULQ-UHFFFAOYSA-N ethyl 2h-pyrimidine-1-carboxylate Chemical compound CCOC(=O)N1CN=CC=C1 XHUWDDXMORFULQ-UHFFFAOYSA-N 0.000 description 1
RJXGRMMBDZNHCE-UHFFFAOYSA-N ethyl 3-bromo-7-(3,4-dimethoxyphenyl)-2-phenyl-1,2,3,3a-tetrahydropyrazolo[1,5-a]pyrimidine-5-carboxylate Chemical compound C=1C(C(=O)OCC)=NC2C(Br)C(C=3C=CC=CC=3)NN2C=1C1=CC=C(OC)C(OC)=C1 RJXGRMMBDZNHCE-UHFFFAOYSA-N 0.000 description 1
LUARVMRUAJRPHZ-UHFFFAOYSA-N ethyl 3-bromo-7-(4-methoxyphenyl)-1,2,3,3a-tetrahydropyrazolo[1,5-a]pyrimidine-5-carboxylate Chemical compound C=1C(C(=O)OCC)=NC2C(Br)CNN2C=1C1=CC=C(OC)C=C1 LUARVMRUAJRPHZ-UHFFFAOYSA-N 0.000 description 1
RPGMOKOIZGJCNI-UHFFFAOYSA-N ethyl 3-cyano-7-(3,4-dimethoxyphenyl)-2-methylsulfanyl-1,2,3,3a-tetrahydropyrazolo[1,5-a]pyrimidine-5-carboxylate Chemical compound C=1C(C(=O)OCC)=NC2C(C#N)C(SC)NN2C=1C1=CC=C(OC)C(OC)=C1 RPGMOKOIZGJCNI-UHFFFAOYSA-N 0.000 description 1
RWJDXBSBYOYYIO-UHFFFAOYSA-N ethyl 5-(4-hydroxy-3-methoxyphenyl)-7-phenylsulfanyl-1,2,3,3a-tetrahydropyrazolo[1,5-a]pyrimidine-3-carboxylate Chemical compound CCOC(=O)C1CNN2C1N=C(C=1C=C(OC)C(O)=CC=1)C=C2SC1=CC=CC=C1 RWJDXBSBYOYYIO-UHFFFAOYSA-N 0.000 description 1
QSJDZVJOFBHAAR-UHFFFAOYSA-N ethyl 5-benzoyl-7-(3,4-dimethoxyphenyl)-1,2,3,3a-tetrahydropyrazolo[1,5-a]pyrimidine-3-carboxylate Chemical compound CCOC(=O)C1CNN2C1N=C(C(=O)C=1C=CC=CC=1)C=C2C1=CC=C(OC)C(OC)=C1 QSJDZVJOFBHAAR-UHFFFAOYSA-N 0.000 description 1
GVGCDHFBWGHAPY-UHFFFAOYSA-N ethyl 5-benzoyl-7-(3-fluorophenyl)-1,2,3,3a-tetrahydropyrazolo[1,5-a]pyrimidine-3-carboxylate Chemical compound CCOC(=O)C1CNN2C1N=C(C(=O)C=1C=CC=CC=1)C=C2C1=CC=CC(F)=C1 GVGCDHFBWGHAPY-UHFFFAOYSA-N 0.000 description 1
WRQMSJDKWUCEED-UHFFFAOYSA-N ethyl 5-benzoyl-7-(4-methoxyphenyl)-1,2,3,3a-tetrahydropyrazolo[1,5-a]pyrimidine-3-carboxylate Chemical compound CCOC(=O)C1CNN2C1N=C(C(=O)C=1C=CC=CC=1)C=C2C1=CC=C(OC)C=C1 WRQMSJDKWUCEED-UHFFFAOYSA-N 0.000 description 1
IQHCBLYGESICGG-UHFFFAOYSA-N ethyl 5-cyclohexyl-7-cyclohexyloxy-1,2,3,3a-tetrahydropyrazolo[1,5-a]pyrimidine-3-carboxylate Chemical compound CCOC(=O)C1CNN2C1N=C(C1CCCCC1)C=C2OC1CCCCC1 IQHCBLYGESICGG-UHFFFAOYSA-N 0.000 description 1
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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
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- 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
- A61P13/02—Drugs for disorders of the urinary system of urine or of the urinary tract, e.g. urine acidifiers
- A—HUMAN NECESSITIES
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- C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
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Heart & Thoracic Surgery (AREA)
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Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Plural Heterocyclic Compounds (AREA)
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SK1154-2003A 2001-03-14 2002-03-13 Substituované pyrazolopyrimidíny a tiazolopyrimidíny, spôsob ich výroby, liečivá tieto látky obsahujúce a ich použitie SK11542003A3 (sk)

Applications Claiming Priority (3)

Application Number	Priority Date	Filing Date	Title
DE2001112197 DE10112197A1 (de)	2001-03-14	2001-03-14	Substituierte Pyrazolo- und Thiazolopyrimidine
DE2001153344 DE10153344A1 (de)	2001-10-29	2001-10-29	Verwendung von substituierten Pyrazolopyrimidinen als Liganden von Nucleosid-Transport-Proteinen und/oder von Purinorezeptoren
PCT/EP2002/002722 WO2002072585A2 (fr)	2001-03-14	2002-03-13	Pyrazolopyrimidines et thiazolopyrimidines substituees

Publications (1)

Publication Number	Publication Date
SK11542003A3 true SK11542003A3 (sk)	2004-07-07

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SK1154-2003A SK11542003A3 (sk)	2001-03-14	2002-03-13	Substituované pyrazolopyrimidíny a tiazolopyrimidíny, spôsob ich výroby, liečivá tieto látky obsahujúce a ich použitie

Country Status (24)

Country	Link
US (1)	US7135568B2 (fr)
EP (2)	EP1637533B1 (fr)
JP (1)	JP2004527508A (fr)
KR (1)	KR20030082982A (fr)
CN (1)	CN1318422C (fr)
AT (2)	ATE404568T1 (fr)
AU (1)	AU2002302419B2 (fr)
BR (1)	BR0208244A (fr)
CA (1)	CA2440760C (fr)
CY (1)	CY1105507T1 (fr)
CZ (1)	CZ20032474A3 (fr)
DE (2)	DE50212652D1 (fr)
DK (1)	DK1368355T3 (fr)
ES (2)	ES2311920T3 (fr)
HU (1)	HUP0401211A3 (fr)
IL (2)	IL157895A0 (fr)
MX (1)	MXPA03008291A (fr)
NO (1)	NO20034031L (fr)
NZ (2)	NZ540574A (fr)
PL (1)	PL364388A1 (fr)
PT (1)	PT1368355E (fr)
RU (1)	RU2003129060A (fr)
SK (1)	SK11542003A3 (fr)
WO (1)	WO2002072585A2 (fr)

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EA017818B1 (ru) *	2008-01-24	2013-03-29	Андрей Александрович ИВАЩЕНКО	ЗАМЕЩЕННЫЕ ЦИКЛОАЛКАНО[e ИЛИ d]ПИРАЗОЛО[1,5-a]ПИРИМИДИНЫ - АНТАГОНИСТЫ СЕРОТОНИНОВЫХ 5-НТРЕЦЕПТОРОВ, СПОСОБЫ ИХ ПОЛУЧЕНИЯ И ПРИМЕНЕНИЯ
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JP5584626B2 (ja) *	2008-01-24	2014-09-03	アンドレイ・アレクサンドロビッチ・イワシェンコ	２−アルキルアミノ−３−（アリールスルホニル）−シクロアルキル［ｅ又はｄ］ピラゾロ［１，５−ａ］ピリミジン−セロトニン５−ＨＴ６受容体アンタゴニスト、その調製の方法及び使用
RU2376291C1 (ru) *	2008-05-07	2009-12-20	Андрей Александрович Иващенко	ЗАМЕЩЕННЫЕ 3,5-ДИАМИНО-4-СУЛЬФОНИЛ-ПИРАЗОЛЫ И 2-АМИНО-3-СУЛЬФОНИЛ-ПИРАЗОЛО[1,5-a]ПИРИМИДИНЫ - АНТАГОНИСТЫ СЕРОТОНИНОВЫХ 5-HT6 РЕЦЕПТОРОВ, СПОСОБЫ ИХ ПОЛУЧЕНИЯ И ПРИМЕНЕНИЯ
RU2369600C1 (ru) *	2008-01-24	2009-10-10	Андрей Александрович Иващенко	ЗАМЕЩЕННЫЕ 4-СУЛЬФОНИЛ-ПИРАЗОЛЫ И 3-СУЛЬФОНИЛ-ПИРАЗОЛО[1,5-a]ПИРИМИДИНЫ - АНТАГОНИСТЫ СЕРОТОНИНОВЫХ5-HT6 РЕЦЕПТОРОВ, АКТИВНЫЙ КОМПОНЕНТ, ФАРМАЦЕВТИЧЕСКАЯ КОМПОЗИЦИЯ, ЛЕКАРСТВЕННОЕ СРЕДСТВО И СПОСОБЫ ИХ ПОЛУЧЕНИЯ
CA2755968C (fr) *	2008-10-06	2019-03-19	Andrey Alexandrovich Ivashchenko	3-arylsulfonyl-pyrazolo[1,5-a]pyrimidines substituees, antagonistes des recepteurs 5-ht6 de serotonine, procedes de fabrication et d'utilisation
AU2009330234A1 (en) *	2008-12-22	2011-07-07	Merck Sharp & Dohme Corp.	Gamma secretase modulators
JO3407B1 (ar)	2012-05-31	2019-10-20	Eisai R&D Man Co Ltd	مركبات رباعي هيدرو بيرازولو بيريميدين
CN102775412B (zh) *	2012-08-21	2013-05-01	四川大学	一种镇静催眠的化合物及其制备方法和用途
CN102977106B (zh) *	2012-12-12	2014-12-10	中国药科大学	一类具有外周镇痛作用的κ阿片受体激动剂
RU2669367C2 (ru) *	2013-03-15	2018-10-11	Хромоселл Корпорейшн	Модуляторы натриевого канала для лечения боли
KR20160054570A (ko) *	2013-09-10	2016-05-16	크로모셀 코포레이션	통증과 당뇨병의 치료를 위한 나트륨 통로 조절인자
US10526323B2 (en)	2015-01-30	2020-01-07	Vanderbilt University	Indazole and azaindazole substituted compounds as mGluR4 allosteric potentiators, compositions, and methods of treating neurological dysfunction
KR102684436B1 (ko)	2015-10-16	2024-07-15	에자이 알앤드디 매니지먼트 가부시키가이샤	Ep4 길항제
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DE10112197A1 (de)	2001-03-14	2002-09-19	Gruenenthal Gmbh	Substituierte Pyrazolo- und Thiazolopyrimidine

2002
- 2002-03-13 ES ES05026811T patent/ES2311920T3/es not_active Expired - Lifetime
- 2002-03-13 IL IL15789502A patent/IL157895A0/xx unknown
- 2002-03-13 RU RU2003129060/04A patent/RU2003129060A/ru not_active Application Discontinuation
- 2002-03-13 EP EP05026811A patent/EP1637533B1/fr not_active Expired - Lifetime
- 2002-03-13 NZ NZ540574A patent/NZ540574A/en unknown
- 2002-03-13 KR KR10-2003-7011953A patent/KR20030082982A/ko not_active Withdrawn
- 2002-03-13 EP EP02729998A patent/EP1368355B1/fr not_active Expired - Lifetime
- 2002-03-13 CZ CZ20032474A patent/CZ20032474A3/cs unknown
- 2002-03-13 BR BR0208244-6A patent/BR0208244A/pt not_active Application Discontinuation
- 2002-03-13 AT AT05026811T patent/ATE404568T1/de not_active IP Right Cessation
- 2002-03-13 NZ NZ528639A patent/NZ528639A/en unknown
- 2002-03-13 CA CA2440760A patent/CA2440760C/fr not_active Expired - Fee Related
- 2002-03-13 WO PCT/EP2002/002722 patent/WO2002072585A2/fr not_active Ceased
- 2002-03-13 PT PT02729998T patent/PT1368355E/pt unknown
- 2002-03-13 DK DK02729998T patent/DK1368355T3/da active
- 2002-03-13 JP JP2002571501A patent/JP2004527508A/ja active Pending
- 2002-03-13 AU AU2002302419A patent/AU2002302419B2/en not_active Ceased
- 2002-03-13 SK SK1154-2003A patent/SK11542003A3/sk unknown
- 2002-03-13 PL PL02364388A patent/PL364388A1/xx not_active Application Discontinuation
- 2002-03-13 DE DE50212652T patent/DE50212652D1/de not_active Expired - Lifetime
- 2002-03-13 HU HU0401211A patent/HUP0401211A3/hu unknown
- 2002-03-13 DE DE50207103T patent/DE50207103D1/de not_active Expired - Lifetime
- 2002-03-13 AT AT02729998T patent/ATE328886T1/de not_active IP Right Cessation
- 2002-03-13 MX MXPA03008291A patent/MXPA03008291A/es active IP Right Grant
- 2002-03-13 CN CNB028096886A patent/CN1318422C/zh not_active Expired - Fee Related
- 2002-03-13 ES ES02729998T patent/ES2263779T3/es not_active Expired - Lifetime
2003
- 2003-09-11 NO NO20034031A patent/NO20034031L/no not_active Application Discontinuation
- 2003-09-11 IL IL157895A patent/IL157895A/en not_active IP Right Cessation
- 2003-09-12 US US10/660,794 patent/US7135568B2/en not_active Expired - Fee Related
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Also Published As

Publication number	Publication date
ATE404568T1 (de)	2008-08-15
ES2311920T3 (es)	2009-02-16
US20040127508A1 (en)	2004-07-01
CA2440760C (fr)	2010-02-09
MXPA03008291A (es)	2003-12-11
DK1368355T3 (da)	2006-10-09
WO2002072585A2 (fr)	2002-09-19
US7135568B2 (en)	2006-11-14
ATE328886T1 (de)	2006-06-15
HUP0401211A2 (hu)	2004-10-28
EP1368355B1 (fr)	2006-06-07
NZ528639A (en)	2005-07-29
NZ540574A (en)	2006-11-30
CN1318422C (zh)	2007-05-30
NO20034031D0 (no)	2003-09-11
IL157895A (en)	2009-12-24
NO20034031L (no)	2003-10-21
PL364388A1 (en)	2004-12-13
CN1507447A (zh)	2004-06-23
AU2002302419B2 (en)	2007-01-18
DE50207103D1 (en)	2006-07-20
HK1061034A1 (en)	2004-09-03
HUP0401211A3 (en)	2008-03-28
DE50212652D1 (de)	2008-09-25
PT1368355E (pt)	2006-09-29
WO2002072585A3 (fr)	2003-02-20
IL157895A0 (en)	2004-03-28
EP1637533B1 (fr)	2008-08-13
EP1637533A1 (fr)	2006-03-22
CZ20032474A3 (cs)	2003-12-17
KR20030082982A (ko)	2003-10-23
CA2440760A1 (fr)	2002-09-19
BR0208244A (pt)	2004-03-02
EP1368355A2 (fr)	2003-12-10
ES2263779T3 (es)	2006-12-16
RU2003129060A (ru)	2005-04-10
CY1105507T1 (el)	2010-04-28
JP2004527508A (ja)	2004-09-09

Publication	Publication Date	Title
SK11542003A3 (sk)	2004-07-07	Substituované pyrazolopyrimidíny a tiazolopyrimidíny, spôsob ich výroby, liečivá tieto látky obsahujúce a ich použitie
KR101878888B1 (ko)	2018-08-17	신규한 ｎｋ-3 수용체 선택적 길항제 화합물, ｎｋ-3 수용체 매개형 질환에 사용되기 위한 의약 조성물 및 방법
CN104884458B (zh)	2017-04-12	作为蛋白质激酶抑制剂的稠合杂环化合物
KR101499308B1 (ko)	2015-03-05	가용성 구아닐레이트 시클라제 활성화제
KR102021159B1 (ko)	2019-09-11	트리시클릭 헤테로시클릭 화합물 및 jak 저해제
AU2019296085B2 (en)	2024-02-15	Heterocyclic compound as TRK inhibitor
WO2009059272A1 (fr)	2009-05-07	Thiénopyrimidines, thiénopyridines et pyrrolopyrimidines en tant qu'inhibiteurs de b-raf
AU5757999A (en)	2000-04-10	(1,2,4)triazolo(1,5-c)pyrimidine derivatives
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