KR20010108394A - 신규 화합물 - Google Patents
신규 화합물 Download PDFInfo
- Publication number
- KR20010108394A KR20010108394A KR1020017012174A KR20017012174A KR20010108394A KR 20010108394 A KR20010108394 A KR 20010108394A KR 1020017012174 A KR1020017012174 A KR 1020017012174A KR 20017012174 A KR20017012174 A KR 20017012174A KR 20010108394 A KR20010108394 A KR 20010108394A
- Authority
- KR
- South Korea
- Prior art keywords
- piperidinyl
- ethyl
- dichlorophenoxy
- amino
- methyl
- 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.)
- Withdrawn
Links
- 150000001875 compounds Chemical class 0.000 title claims abstract description 99
- 229910052757 nitrogen Inorganic materials 0.000 claims abstract description 26
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 22
- 125000004433 nitrogen atom Chemical group N* 0.000 claims abstract description 17
- 238000000034 method Methods 0.000 claims abstract description 15
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 13
- 125000004122 cyclic group Chemical group 0.000 claims abstract description 10
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 10
- 239000008194 pharmaceutical composition Substances 0.000 claims abstract description 9
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims abstract description 8
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 8
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims abstract description 7
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 7
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims abstract description 7
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims abstract description 6
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims abstract description 6
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 6
- 125000005842 heteroatom Chemical group 0.000 claims abstract description 6
- 239000001301 oxygen Substances 0.000 claims abstract description 6
- 125000004430 oxygen atom Chemical group O* 0.000 claims abstract description 6
- 229920006395 saturated elastomer Polymers 0.000 claims abstract description 6
- 229910052717 sulfur Inorganic materials 0.000 claims abstract description 6
- 239000011593 sulfur Substances 0.000 claims abstract description 6
- 238000002560 therapeutic procedure Methods 0.000 claims abstract description 6
- 125000000623 heterocyclic group Chemical group 0.000 claims abstract description 4
- -1 cyano, hydroxyl Chemical group 0.000 claims description 234
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 133
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 35
- 150000003839 salts Chemical class 0.000 claims description 23
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 20
- 239000012453 solvate Substances 0.000 claims description 19
- 125000001424 substituent group Chemical group 0.000 claims description 16
- 125000005843 halogen group Chemical group 0.000 claims description 15
- 201000010099 disease Diseases 0.000 claims description 10
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 10
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims description 9
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 9
- 125000000217 alkyl group Chemical group 0.000 claims description 7
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 claims description 7
- 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 claims description 6
- 125000000242 4-chlorobenzoyl group Chemical group ClC1=CC=C(C(=O)*)C=C1 0.000 claims description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N EtOH Substances CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 6
- BPPZIPHINXIUFJ-UHFFFAOYSA-N [1-[2-[(5-chloro-1,3-dimethylpyrazol-4-yl)methylamino]ethyl]piperidin-4-yl]-(4-chlorophenyl)methanone Chemical compound CC1=NN(C)C(Cl)=C1CNCCN1CCC(C(=O)C=2C=CC(Cl)=CC=2)CC1 BPPZIPHINXIUFJ-UHFFFAOYSA-N 0.000 claims description 6
- 125000002541 furyl group Chemical group 0.000 claims description 6
- 238000004519 manufacturing process Methods 0.000 claims description 6
- MHIFSXJQGYPPDB-UHFFFAOYSA-N n-[2-[4-(3,4-dichlorophenoxy)piperidin-1-yl]ethyl]-4-fluorobenzamide Chemical compound C1=CC(F)=CC=C1C(=O)NCCN1CCC(OC=2C=C(Cl)C(Cl)=CC=2)CC1 MHIFSXJQGYPPDB-UHFFFAOYSA-N 0.000 claims description 6
- FTAFETTVRQXSRZ-UHFFFAOYSA-N n-[2-[4-(3,4-dichlorophenoxy)piperidin-1-yl]ethyl]-4-methoxybenzamide Chemical compound C1=CC(OC)=CC=C1C(=O)NCCN1CCC(OC=2C=C(Cl)C(Cl)=CC=2)CC1 FTAFETTVRQXSRZ-UHFFFAOYSA-N 0.000 claims description 6
- 125000001544 thienyl group Chemical group 0.000 claims description 6
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims description 5
- 125000004454 (C1-C6) alkoxycarbonyl group Chemical group 0.000 claims description 5
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims description 5
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims description 5
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 5
- 239000003085 diluting agent Substances 0.000 claims description 5
- 230000000694 effects Effects 0.000 claims description 5
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 5
- 239000000546 pharmaceutical excipient Substances 0.000 claims description 5
- 125000004076 pyridyl group Chemical group 0.000 claims description 5
- 125000005030 pyridylthio group Chemical group N1=C(C=CC=C1)S* 0.000 claims description 5
- 125000005420 sulfonamido group Chemical group S(=O)(=O)(N*)* 0.000 claims description 5
- 125000006700 (C1-C6) alkylthio group Chemical group 0.000 claims description 4
- ZJWLHFWEFOMZAL-UHFFFAOYSA-N 3-[2-[4-(3,4-dichlorophenoxy)piperidin-1-yl]ethyl]-6-methoxy-1h-quinazoline-2,4-dione Chemical compound O=C1C2=CC(OC)=CC=C2NC(=O)N1CCN(CC1)CCC1OC1=CC=C(Cl)C(Cl)=C1 ZJWLHFWEFOMZAL-UHFFFAOYSA-N 0.000 claims description 4
- QCQCHGYLTSGIGX-GHXANHINSA-N 4-[[(3ar,5ar,5br,7ar,9s,11ar,11br,13as)-5a,5b,8,8,11a-pentamethyl-3a-[(5-methylpyridine-3-carbonyl)amino]-2-oxo-1-propan-2-yl-4,5,6,7,7a,9,10,11,11b,12,13,13a-dodecahydro-3h-cyclopenta[a]chrysen-9-yl]oxy]-2,2-dimethyl-4-oxobutanoic acid Chemical compound N([C@@]12CC[C@@]3(C)[C@]4(C)CC[C@H]5C(C)(C)[C@@H](OC(=O)CC(C)(C)C(O)=O)CC[C@]5(C)[C@H]4CC[C@@H]3C1=C(C(C2)=O)C(C)C)C(=O)C1=CN=CC(C)=C1 QCQCHGYLTSGIGX-GHXANHINSA-N 0.000 claims description 4
- MSLRDSZTCIDZOZ-UHFFFAOYSA-N 4-chloro-n-[2-[4-(3,4-dichlorophenoxy)piperidin-1-yl]ethyl]-2-[2-(dimethylamino)-2-oxoethoxy]benzamide Chemical compound CN(C)C(=O)COC1=CC(Cl)=CC=C1C(=O)NCCN1CCC(OC=2C=C(Cl)C(Cl)=CC=2)CC1 MSLRDSZTCIDZOZ-UHFFFAOYSA-N 0.000 claims description 4
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 4
- RATAYRRRZOWEPY-UHFFFAOYSA-N N-[1-[4-(3,4-dichlorophenoxy)piperidin-1-yl]-3-methylbutan-2-yl]-4-methylbenzamide hydrochloride Chemical class Cl.CC(C)C(CN1CCC(CC1)Oc1ccc(Cl)c(Cl)c1)NC(=O)c1ccc(C)cc1 RATAYRRRZOWEPY-UHFFFAOYSA-N 0.000 claims description 4
- 239000000460 chlorine Substances 0.000 claims description 4
- 229910052801 chlorine Inorganic materials 0.000 claims description 4
- 239000003814 drug Substances 0.000 claims description 4
- 239000001257 hydrogen Substances 0.000 claims description 4
- 229910052739 hydrogen Inorganic materials 0.000 claims description 4
- 208000027866 inflammatory disease Diseases 0.000 claims description 4
- KETMPDYDKCWDQW-UHFFFAOYSA-N n-[2-[4-(3,4-dichloroanilino)piperidin-1-yl]ethyl]-3-methoxybenzamide;dihydrochloride Chemical compound Cl.Cl.COC1=CC=CC(C(=O)NCCN2CCC(CC2)NC=2C=C(Cl)C(Cl)=CC=2)=C1 KETMPDYDKCWDQW-UHFFFAOYSA-N 0.000 claims description 4
- NVFNOMAXNHPMEV-UHFFFAOYSA-N n-[2-[4-(3,4-dichlorobenzoyl)piperazin-1-yl]ethyl]-3-methoxybenzamide;hydrochloride Chemical compound Cl.COC1=CC=CC(C(=O)NCCN2CCN(CC2)C(=O)C=2C=C(Cl)C(Cl)=CC=2)=C1 NVFNOMAXNHPMEV-UHFFFAOYSA-N 0.000 claims description 4
- ZZOZJHGDXJFENS-UHFFFAOYSA-N n-[2-[4-(4-chlorobenzoyl)piperidin-1-yl]ethyl]-3-[2-(methylamino)-2-oxoethoxy]benzamide;hydrochloride Chemical compound Cl.CNC(=O)COC1=CC=CC(C(=O)NCCN2CCC(CC2)C(=O)C=2C=CC(Cl)=CC=2)=C1 ZZOZJHGDXJFENS-UHFFFAOYSA-N 0.000 claims description 4
- QGUVTCMYSOSXFE-UHFFFAOYSA-N n-[3-[4-(3,4-dichlorophenoxy)piperidin-1-yl]propyl]-1-methylpyrazolo[3,4-d]pyrimidin-4-amine Chemical compound N1=CN=C2N(C)N=CC2=C1NCCCN(CC1)CCC1OC1=CC=C(Cl)C(Cl)=C1 QGUVTCMYSOSXFE-UHFFFAOYSA-N 0.000 claims description 4
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 4
- CCEKWQBFPXXKBN-UHFFFAOYSA-N (4-chlorophenyl)-[1-[2-(2-methylpropylamino)ethyl]piperidin-4-yl]methanone Chemical compound C1CN(CCNCC(C)C)CCC1C(=O)C1=CC=C(Cl)C=C1 CCEKWQBFPXXKBN-UHFFFAOYSA-N 0.000 claims description 3
- QWDIDFWRSBMBFV-UHFFFAOYSA-N (4-chlorophenyl)-[1-[2-(3-methylsulfanylbutylamino)ethyl]piperidin-4-yl]methanone Chemical compound C1CN(CCNCCC(C)SC)CCC1C(=O)C1=CC=C(Cl)C=C1 QWDIDFWRSBMBFV-UHFFFAOYSA-N 0.000 claims description 3
- CBFALSMXAFBKBY-UHFFFAOYSA-N (4-chlorophenyl)-[1-[2-(pyridin-2-ylmethylamino)ethyl]piperidin-4-yl]methanone Chemical compound C1=CC(Cl)=CC=C1C(=O)C1CCN(CCNCC=2N=CC=CC=2)CC1 CBFALSMXAFBKBY-UHFFFAOYSA-N 0.000 claims description 3
- HIRXHSWOYNEDIE-UHFFFAOYSA-N (4-chlorophenyl)-[1-[2-(pyridin-4-ylmethylamino)ethyl]piperidin-4-yl]methanone Chemical compound C1=CC(Cl)=CC=C1C(=O)C1CCN(CCNCC=2C=CN=CC=2)CC1 HIRXHSWOYNEDIE-UHFFFAOYSA-N 0.000 claims description 3
- DPZYXLJALIJPHJ-UHFFFAOYSA-N (4-chlorophenyl)-[1-[2-(quinolin-3-ylmethylamino)ethyl]piperidin-4-yl]methanone Chemical compound C1=CC(Cl)=CC=C1C(=O)C1CCN(CCNCC=2C=C3C=CC=CC3=NC=2)CC1 DPZYXLJALIJPHJ-UHFFFAOYSA-N 0.000 claims description 3
- RMTAXKXHFKSHPJ-UHFFFAOYSA-N (4-chlorophenyl)-[1-[2-[(2,4-dimethoxypyrimidin-5-yl)methylamino]ethyl]piperidin-4-yl]methanone Chemical compound COC1=NC(OC)=NC=C1CNCCN1CCC(C(=O)C=2C=CC(Cl)=CC=2)CC1 RMTAXKXHFKSHPJ-UHFFFAOYSA-N 0.000 claims description 3
- BZZQZDAWAXXDRW-UHFFFAOYSA-N (4-chlorophenyl)-[1-[2-[(2,5-difluorophenyl)methylamino]ethyl]piperidin-4-yl]methanone Chemical compound FC1=CC=C(F)C(CNCCN2CCC(CC2)C(=O)C=2C=CC(Cl)=CC=2)=C1 BZZQZDAWAXXDRW-UHFFFAOYSA-N 0.000 claims description 3
- QNHDEZAQQYUODX-UHFFFAOYSA-N (4-chlorophenyl)-[1-[2-[(2,6-dichlorophenyl)methylamino]ethyl]piperidin-4-yl]methanone Chemical compound C1=CC(Cl)=CC=C1C(=O)C1CCN(CCNCC=2C(=CC=CC=2Cl)Cl)CC1 QNHDEZAQQYUODX-UHFFFAOYSA-N 0.000 claims description 3
- PLIWJSGXSUYJCZ-UHFFFAOYSA-N (4-chlorophenyl)-[1-[2-[(2,6-dichloropyridin-4-yl)methylamino]ethyl]piperidin-4-yl]methanone Chemical compound C1=CC(Cl)=CC=C1C(=O)C1CCN(CCNCC=2C=C(Cl)N=C(Cl)C=2)CC1 PLIWJSGXSUYJCZ-UHFFFAOYSA-N 0.000 claims description 3
- FIHOVKRJUWICRZ-UHFFFAOYSA-N (4-chlorophenyl)-[1-[2-[(2-chloroquinolin-3-yl)methylamino]ethyl]piperidin-4-yl]methanone Chemical compound C1=CC(Cl)=CC=C1C(=O)C1CCN(CCNCC=2C(=NC3=CC=CC=C3C=2)Cl)CC1 FIHOVKRJUWICRZ-UHFFFAOYSA-N 0.000 claims description 3
- CCKAMSOSAWJYBF-UHFFFAOYSA-N (4-chlorophenyl)-[1-[2-[(2-fluoro-4,5-dimethoxyphenyl)methylamino]ethyl]piperidin-4-yl]methanone Chemical compound C1=C(OC)C(OC)=CC(F)=C1CNCCN1CCC(C(=O)C=2C=CC(Cl)=CC=2)CC1 CCKAMSOSAWJYBF-UHFFFAOYSA-N 0.000 claims description 3
- FBZOJNNRWXMQGT-UHFFFAOYSA-N (4-chlorophenyl)-[1-[2-[(2-phenyl-1h-imidazol-5-yl)methylamino]ethyl]piperidin-4-yl]methanone Chemical compound C1=CC(Cl)=CC=C1C(=O)C1CCN(CCNCC=2N=C(NC=2)C=2C=CC=CC=2)CC1 FBZOJNNRWXMQGT-UHFFFAOYSA-N 0.000 claims description 3
- CRHYLKKTXOMRKU-UHFFFAOYSA-N (4-chlorophenyl)-[1-[2-[(2-phenylpyrazol-3-yl)methylamino]ethyl]piperidin-4-yl]methanone Chemical compound C1=CC(Cl)=CC=C1C(=O)C1CCN(CCNCC=2N(N=CC=2)C=2C=CC=CC=2)CC1 CRHYLKKTXOMRKU-UHFFFAOYSA-N 0.000 claims description 3
- NIRSYNGGTPBPRP-UHFFFAOYSA-N (4-chlorophenyl)-[1-[2-[(3,4,5-trimethoxyphenyl)methylamino]ethyl]piperidin-4-yl]methanone Chemical compound COC1=C(OC)C(OC)=CC(CNCCN2CCC(CC2)C(=O)C=2C=CC(Cl)=CC=2)=C1 NIRSYNGGTPBPRP-UHFFFAOYSA-N 0.000 claims description 3
- BQSJOJBQVLBVLW-UHFFFAOYSA-N (4-chlorophenyl)-[1-[2-[(3,5-difluorophenyl)methylamino]ethyl]piperidin-4-yl]methanone Chemical compound FC1=CC(F)=CC(CNCCN2CCC(CC2)C(=O)C=2C=CC(Cl)=CC=2)=C1 BQSJOJBQVLBVLW-UHFFFAOYSA-N 0.000 claims description 3
- GQWDJTMFSZHGMX-UHFFFAOYSA-N (4-chlorophenyl)-[1-[2-[(3-hydroxy-4-methoxyphenyl)methylamino]ethyl]piperidin-4-yl]methanone Chemical compound C1=C(O)C(OC)=CC=C1CNCCN1CCC(C(=O)C=2C=CC(Cl)=CC=2)CC1 GQWDJTMFSZHGMX-UHFFFAOYSA-N 0.000 claims description 3
- NTICZMKTSNVWMT-UHFFFAOYSA-N (4-chlorophenyl)-[1-[2-[(3-hydroxy-4-nitrophenyl)methylamino]ethyl]piperidin-4-yl]methanone Chemical compound C1=C([N+]([O-])=O)C(O)=CC(CNCCN2CCC(CC2)C(=O)C=2C=CC(Cl)=CC=2)=C1 NTICZMKTSNVWMT-UHFFFAOYSA-N 0.000 claims description 3
- IRHNODZMYZXIQC-UHFFFAOYSA-N (4-chlorophenyl)-[1-[2-[(3-nitro-4-pyridin-2-ylsulfanylphenyl)methylamino]ethyl]piperidin-4-yl]methanone Chemical compound C=1C=C(SC=2N=CC=CC=2)C([N+](=O)[O-])=CC=1CNCCN(CC1)CCC1C(=O)C1=CC=C(Cl)C=C1 IRHNODZMYZXIQC-UHFFFAOYSA-N 0.000 claims description 3
- SNSLWGMYHQXIKB-UHFFFAOYSA-N (4-chlorophenyl)-[1-[2-[(4-nitrophenyl)methylamino]ethyl]piperidin-4-yl]methanone Chemical compound C1=CC([N+](=O)[O-])=CC=C1CNCCN1CCC(C(=O)C=2C=CC(Cl)=CC=2)CC1 SNSLWGMYHQXIKB-UHFFFAOYSA-N 0.000 claims description 3
- LALDGZAOEXVHEY-UHFFFAOYSA-N (4-chlorophenyl)-[1-[2-[(4-phenylpiperidin-4-yl)methylamino]ethyl]piperidin-4-yl]methanone Chemical compound C1=CC(Cl)=CC=C1C(=O)C1CCN(CCNCC2(CCNCC2)C=2C=CC=CC=2)CC1 LALDGZAOEXVHEY-UHFFFAOYSA-N 0.000 claims description 3
- OVNYNSHJGJUENX-UHFFFAOYSA-N (4-chlorophenyl)-[1-[2-[(5-nitro-2-pyridin-2-ylsulfanylphenyl)methylamino]ethyl]piperidin-4-yl]methanone Chemical compound C1CC(C(=O)C=2C=CC(Cl)=CC=2)CCN1CCNCC1=CC([N+](=O)[O-])=CC=C1SC1=CC=CC=N1 OVNYNSHJGJUENX-UHFFFAOYSA-N 0.000 claims description 3
- LQNLIYRHRPZSPL-UHFFFAOYSA-N (4-chlorophenyl)-[1-[2-[(6-nitro-1,3-benzodioxol-5-yl)methylamino]ethyl]piperidin-4-yl]methanone Chemical compound [O-][N+](=O)C1=CC=2OCOC=2C=C1CNCCN(CC1)CCC1C(=O)C1=CC=C(Cl)C=C1 LQNLIYRHRPZSPL-UHFFFAOYSA-N 0.000 claims description 3
- PFYFSSBSMWQHOT-UHFFFAOYSA-N (4-chlorophenyl)-[1-[2-[(7-hydroxy-3,7-dimethyloctyl)amino]ethyl]piperidin-4-yl]methanone Chemical compound C1CN(CCNCCC(CCCC(C)(C)O)C)CCC1C(=O)C1=CC=C(Cl)C=C1 PFYFSSBSMWQHOT-UHFFFAOYSA-N 0.000 claims description 3
- USCYTAXQSSZRJK-OWOJBTEDSA-N (4-chlorophenyl)-[1-[2-[[(e)-3-(4-nitrophenyl)prop-2-enyl]amino]ethyl]piperidin-4-yl]methanone Chemical compound C1=CC([N+](=O)[O-])=CC=C1\C=C\CNCCN1CCC(C(=O)C=2C=CC(Cl)=CC=2)CC1 USCYTAXQSSZRJK-OWOJBTEDSA-N 0.000 claims description 3
- NTMOXDJIDPKQKQ-UHFFFAOYSA-N (4-chlorophenyl)-[1-[2-[[5-(3-nitrophenyl)furan-2-yl]methylamino]ethyl]piperidin-4-yl]methanone Chemical compound [O-][N+](=O)C1=CC=CC(C=2OC(CNCCN3CCC(CC3)C(=O)C=3C=CC(Cl)=CC=3)=CC=2)=C1 NTMOXDJIDPKQKQ-UHFFFAOYSA-N 0.000 claims description 3
- ZWXDDWDWMCESKH-RMKNXTFCSA-N (e)-n-[2-[4-(3,4-dichlorophenoxy)piperidin-1-yl]ethyl]-3-phenylprop-2-enamide Chemical compound C1=C(Cl)C(Cl)=CC=C1OC1CCN(CCNC(=O)\C=C\C=2C=CC=CC=2)CC1 ZWXDDWDWMCESKH-RMKNXTFCSA-N 0.000 claims description 3
- GNTLPZAHICFRRC-XCVCLJGOSA-N (e)-n-[2-[4-(4-chlorobenzoyl)piperidin-1-yl]ethyl]-3-(4-nitrophenyl)prop-2-enamide Chemical compound C1=CC([N+](=O)[O-])=CC=C1\C=C\C(=O)NCCN1CCC(C(=O)C=2C=CC(Cl)=CC=2)CC1 GNTLPZAHICFRRC-XCVCLJGOSA-N 0.000 claims description 3
- ZOPXEBJEWRETPJ-IZZDOVSWSA-N (e)-n-[2-[4-(4-chlorobenzoyl)piperidin-1-yl]ethyl]-3-phenylprop-2-enamide Chemical compound C1=CC(Cl)=CC=C1C(=O)C1CCN(CCNC(=O)\C=C\C=2C=CC=CC=2)CC1 ZOPXEBJEWRETPJ-IZZDOVSWSA-N 0.000 claims description 3
- GUXFOLSWRZODOX-UHFFFAOYSA-N 2-[3-[2-[4-(4-fluorobenzoyl)piperidin-1-yl]ethyl]-2,4-dioxoquinazolin-1-yl]-n,n-dimethylacetamide;hydrochloride Chemical compound Cl.O=C1N(CC(=O)N(C)C)C2=CC=CC=C2C(=O)N1CCN(CC1)CCC1C(=O)C1=CC=C(F)C=C1 GUXFOLSWRZODOX-UHFFFAOYSA-N 0.000 claims description 3
- XNGVLISOMZWKAQ-UHFFFAOYSA-N 2-[[2-[3-[4-(3,4-dichlorophenoxy)piperidin-1-yl]propylamino]pyrimidin-4-yl]-methylamino]ethanol Chemical compound OCCN(C)C1=CC=NC(NCCCN2CCC(CC2)OC=2C=C(Cl)C(Cl)=CC=2)=N1 XNGVLISOMZWKAQ-UHFFFAOYSA-N 0.000 claims description 3
- OLFUWQFGAVROEA-UHFFFAOYSA-N 2-[[2-[3-[4-(3,4-dichlorophenoxy)piperidin-1-yl]propylamino]pyrimidin-4-yl]amino]ethanol Chemical compound OCCNC1=CC=NC(NCCCN2CCC(CC2)OC=2C=C(Cl)C(Cl)=CC=2)=N1 OLFUWQFGAVROEA-UHFFFAOYSA-N 0.000 claims description 3
- ZNLBTLXZEMUXOG-UHFFFAOYSA-N 2-[[4-[2-[4-(3,4-dichlorophenoxy)piperidin-1-yl]ethylamino]pyrimidin-2-yl]amino]ethanol Chemical compound OCCNC1=NC=CC(NCCN2CCC(CC2)OC=2C=C(Cl)C(Cl)=CC=2)=N1 ZNLBTLXZEMUXOG-UHFFFAOYSA-N 0.000 claims description 3
- SSDVFNNGIZCJGU-UHFFFAOYSA-N 2-[[4-[3-[4-(3,4-dichlorophenoxy)piperidin-1-yl]propylamino]pyrimidin-2-yl]-methylamino]ethanol Chemical compound OCCN(C)C1=NC=CC(NCCCN2CCC(CC2)OC=2C=C(Cl)C(Cl)=CC=2)=N1 SSDVFNNGIZCJGU-UHFFFAOYSA-N 0.000 claims description 3
- QPIPEHZSHGDUEL-UHFFFAOYSA-N 2-acetamido-n-[2-[4-(3,4-dichlorophenoxy)piperidin-1-yl]ethyl]-1,3-thiazole-4-carboxamide Chemical compound S1C(NC(=O)C)=NC(C(=O)NCCN2CCC(CC2)OC=2C=C(Cl)C(Cl)=CC=2)=C1 QPIPEHZSHGDUEL-UHFFFAOYSA-N 0.000 claims description 3
- PFODAJFKGNHIKF-UHFFFAOYSA-N 2-amino-n-[2-[4-(3,4-dichlorophenoxy)piperidin-1-yl]ethyl]-1,3-thiazole-4-carboxamide Chemical compound S1C(N)=NC(C(=O)NCCN2CCC(CC2)OC=2C=C(Cl)C(Cl)=CC=2)=C1 PFODAJFKGNHIKF-UHFFFAOYSA-N 0.000 claims description 3
- WFTYOJFJHQSUGC-UHFFFAOYSA-N 2-bromo-n-[2-[4-(3,4-dichlorophenoxy)piperidin-1-yl]ethyl]-5-methoxybenzamide Chemical compound COC1=CC=C(Br)C(C(=O)NCCN2CCC(CC2)OC=2C=C(Cl)C(Cl)=CC=2)=C1 WFTYOJFJHQSUGC-UHFFFAOYSA-N 0.000 claims description 3
- 125000004182 2-chlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(*)C([H])=C1[H] 0.000 claims description 3
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- WGXSHWPUOPTBSB-UHFFFAOYSA-N tert-butyl n-[2-[4-(3,4-dichlorophenoxy)piperidin-1-yl]ethyl]carbamate Chemical compound C1CN(CCNC(=O)OC(C)(C)C)CCC1OC1=CC=C(Cl)C(Cl)=C1 WGXSHWPUOPTBSB-UHFFFAOYSA-N 0.000 description 1
- 125000000335 thiazolyl group Chemical group 0.000 description 1
- DLFVBJFMPXGRIB-UHFFFAOYSA-N thioacetamide Natural products CC(N)=O DLFVBJFMPXGRIB-UHFFFAOYSA-N 0.000 description 1
- 206010043778 thyroiditis Diseases 0.000 description 1
- 238000002054 transplantation Methods 0.000 description 1
- GPRLSGONYQIRFK-MNYXATJNSA-N triton Chemical compound [3H+] GPRLSGONYQIRFK-MNYXATJNSA-N 0.000 description 1
- 208000001319 vasomotor rhinitis Diseases 0.000 description 1
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- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
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- C07D—HETEROCYCLIC COMPOUNDS
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- C07D211/18—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D211/30—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms with hydrocarbon radicals, substituted by doubly bound oxygen or sulfur atoms or by two oxygen or sulfur atoms singly bound to the same carbon atom
- C07D211/32—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms with hydrocarbon radicals, substituted by doubly bound oxygen or sulfur atoms or by two oxygen or sulfur atoms singly bound to the same carbon atom by oxygen atoms
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- C07D211/36—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D211/40—Oxygen atoms
- C07D211/44—Oxygen atoms attached in position 4
- C07D211/46—Oxygen atoms attached in position 4 having a hydrogen atom as the second substituent in position 4
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- C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D211/36—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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- C07D217/14—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with radicals, substituted by hetero atoms, attached to carbon atoms of the nitrogen-containing ring other than aralkyl radicals
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- C07D295/16—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms
- C07D295/18—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms by radicals derived from carboxylic acids, or sulfur or nitrogen analogues thereof
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- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
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- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
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- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
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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
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| PCT/SE2000/000563 WO2000058305A1 (en) | 1999-03-26 | 2000-03-22 | Novel compounds |
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| TWI329105B (en) | 2002-02-01 | 2010-08-21 | Rigel Pharmaceuticals Inc | 2,4-pyrimidinediamine compounds and their uses |
| TW200303304A (en) | 2002-02-18 | 2003-09-01 | Astrazeneca Ab | Chemical compounds |
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| EE200100502A (et) | 1999-03-26 | 2002-12-16 | Astrazeneca Ab | Ühendid |
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- 2000-03-22 EP EP00921237A patent/EP1165545A1/en not_active Withdrawn
- 2000-03-22 TR TR2001/02800T patent/TR200102800T2/xx unknown
- 2000-03-22 SK SK1182-2001A patent/SK11822001A3/sk unknown
- 2000-03-22 KR KR1020017012174A patent/KR20010108394A/ko not_active Withdrawn
- 2000-03-22 JP JP2000608007A patent/JP2002540204A/ja active Pending
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- 2000-03-22 CZ CZ20013451A patent/CZ20013451A3/cs unknown
- 2000-03-22 BR BR0009338-6A patent/BR0009338A/pt not_active IP Right Cessation
- 2000-03-22 CA CA002361366A patent/CA2361366A1/en not_active Abandoned
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| US20030134840A1 (en) | 2003-07-17 |
| JP2002540204A (ja) | 2002-11-26 |
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| US6518286B1 (en) | 2003-02-11 |
| CN1344266A (zh) | 2002-04-10 |
| EP1165545A1 (en) | 2002-01-02 |
| PL350904A1 (en) | 2003-02-10 |
| HUP0202017A3 (en) | 2003-03-28 |
| SK11822001A3 (sk) | 2002-09-10 |
| TR200102800T2 (tr) | 2002-01-21 |
| CZ20013451A3 (cs) | 2002-04-17 |
| HUP0202017A2 (hu) | 2002-11-28 |
| WO2000058305A1 (en) | 2000-10-05 |
| AU4157500A (en) | 2000-10-16 |
| NO20014518L (no) | 2001-09-17 |
| NO20014518D0 (no) | 2001-09-17 |
| IS6024A (is) | 2001-07-26 |
| EE200100502A (et) | 2002-12-16 |
| CA2361366A1 (en) | 2000-10-05 |
| BR0009338A (pt) | 2001-12-26 |
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