CA2448729A1 - Piperazinyl and piperidyl substituted heterocyclic compounds - Google Patents
Piperazinyl and piperidyl substituted heterocyclic compounds Download PDFInfo
- Publication number
- CA2448729A1 CA2448729A1 CA002448729A CA2448729A CA2448729A1 CA 2448729 A1 CA2448729 A1 CA 2448729A1 CA 002448729 A CA002448729 A CA 002448729A CA 2448729 A CA2448729 A CA 2448729A CA 2448729 A1 CA2448729 A1 CA 2448729A1
- Authority
- CA
- Canada
- Prior art keywords
- pyrazine
- piperazinyl
- mmol
- ethoxy
- oxy
- 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.)
- Abandoned
Links
- -1 piperidyl substituted heterocyclic compounds Chemical class 0.000 title claims description 83
- 125000004193 piperazinyl group Chemical group 0.000 title claims description 10
- 150000001875 compounds Chemical class 0.000 claims abstract description 310
- 238000000034 method Methods 0.000 claims description 155
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 claims description 136
- 229910052739 hydrogen Inorganic materials 0.000 claims description 95
- KYQCOXFCLRTKLS-UHFFFAOYSA-N Pyrazine Chemical compound C1=CN=CC=N1 KYQCOXFCLRTKLS-UHFFFAOYSA-N 0.000 claims description 81
- 229910052757 nitrogen Inorganic materials 0.000 claims description 81
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 58
- PCNDJXKNXGMECE-UHFFFAOYSA-N Phenazine Natural products C1=CC=CC2=NC3=CC=CC=C3N=C21 PCNDJXKNXGMECE-UHFFFAOYSA-N 0.000 claims description 41
- QZAYGJVTTNCVMB-UHFFFAOYSA-N serotonin Chemical compound C1=C(O)C=C2C(CCN)=CNC2=C1 QZAYGJVTTNCVMB-UHFFFAOYSA-N 0.000 claims description 34
- 125000001072 heteroaryl group Chemical group 0.000 claims description 30
- 239000001257 hydrogen Substances 0.000 claims description 29
- 125000003118 aryl group Chemical group 0.000 claims description 27
- 102000006902 5-HT2C Serotonin Receptor Human genes 0.000 claims description 25
- 108010072553 5-HT2C Serotonin Receptor Proteins 0.000 claims description 24
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 22
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 20
- 229910052736 halogen Inorganic materials 0.000 claims description 18
- 150000002367 halogens Chemical class 0.000 claims description 18
- 238000011282 treatment Methods 0.000 claims description 18
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 17
- 150000003839 salts Chemical class 0.000 claims description 17
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 16
- 150000003216 pyrazines Chemical class 0.000 claims description 13
- 208000019901 Anxiety disease Diseases 0.000 claims description 12
- 229940076279 serotonin Drugs 0.000 claims description 12
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 12
- 208000008589 Obesity Diseases 0.000 claims description 11
- 208000035475 disorder Diseases 0.000 claims description 11
- 235000020824 obesity Nutrition 0.000 claims description 11
- 208000030814 Eating disease Diseases 0.000 claims description 10
- 208000019454 Feeding and Eating disease Diseases 0.000 claims description 10
- 235000014632 disordered eating Nutrition 0.000 claims description 10
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 10
- 239000003814 drug Substances 0.000 claims description 9
- 150000003230 pyrimidines Chemical class 0.000 claims description 9
- 206010015037 epilepsy Diseases 0.000 claims description 7
- 125000005553 heteroaryloxy group Chemical group 0.000 claims description 7
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 7
- 150000003222 pyridines Chemical class 0.000 claims description 7
- 201000009032 substance abuse Diseases 0.000 claims description 7
- 231100000736 substance abuse Toxicity 0.000 claims description 7
- 208000011117 substance-related disease Diseases 0.000 claims description 7
- 230000002485 urinary effect Effects 0.000 claims description 7
- 208000026139 Memory disease Diseases 0.000 claims description 6
- 208000019022 Mood disease Diseases 0.000 claims description 6
- 208000002193 Pain Diseases 0.000 claims description 6
- RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 claims description 6
- 201000001880 Sexual dysfunction Diseases 0.000 claims description 6
- 125000005110 aryl thio group Chemical group 0.000 claims description 6
- 125000004104 aryloxy group Chemical group 0.000 claims description 6
- 125000005368 heteroarylthio group Chemical group 0.000 claims description 6
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 6
- 239000008194 pharmaceutical composition Substances 0.000 claims description 6
- 201000000980 schizophrenia Diseases 0.000 claims description 6
- 231100000872 sexual dysfunction Toxicity 0.000 claims description 6
- CUVLQUXETABQKG-UHFFFAOYSA-N 2-(1-phenylethoxy)-6-piperazin-1-ylpyrazine Chemical compound C=1C=CC=CC=1C(C)OC(N=1)=CN=CC=1N1CCNCC1 CUVLQUXETABQKG-UHFFFAOYSA-N 0.000 claims description 5
- VKOLTRJZQDPECX-UHFFFAOYSA-N 2-[(2-methoxyphenyl)methoxy]-6-piperazin-1-ylpyrazine Chemical compound COC1=CC=CC=C1COC1=CN=CC(N2CCNCC2)=N1 VKOLTRJZQDPECX-UHFFFAOYSA-N 0.000 claims description 5
- LBXPCVSYZSEMJR-UHFFFAOYSA-N 2-[(3,5-dimethoxyphenyl)methoxy]-6-piperazin-1-ylpyrazine Chemical compound COC1=CC(OC)=CC(COC=2N=C(C=NC=2)N2CCNCC2)=C1 LBXPCVSYZSEMJR-UHFFFAOYSA-N 0.000 claims description 5
- IBYJQSYRBUBZJX-UHFFFAOYSA-N 2-[(3-methoxyphenyl)methoxy]-6-piperazin-1-ylpyrazine Chemical compound COC1=CC=CC(COC=2N=C(C=NC=2)N2CCNCC2)=C1 IBYJQSYRBUBZJX-UHFFFAOYSA-N 0.000 claims description 5
- VPTFFYNHFALUCC-UHFFFAOYSA-N 2-[1-(2-methoxyphenyl)ethoxy]-6-piperazin-1-ylpyrazine Chemical compound COC1=CC=CC=C1C(C)OC1=CN=CC(N2CCNCC2)=N1 VPTFFYNHFALUCC-UHFFFAOYSA-N 0.000 claims description 5
- VIVXNAQRWKTJPF-UHFFFAOYSA-N 2-[1-(3-fluorophenyl)ethoxy]-6-piperazin-1-ylpyrazine Chemical compound C=1C=CC(F)=CC=1C(C)OC(N=1)=CN=CC=1N1CCNCC1 VIVXNAQRWKTJPF-UHFFFAOYSA-N 0.000 claims description 5
- UXACGMNLBLFPQV-UHFFFAOYSA-N 2-[2-(3-chlorophenyl)ethoxy]-6-piperazin-1-ylpyrazine Chemical compound ClC1=CC=CC(CCOC=2N=C(C=NC=2)N2CCNCC2)=C1 UXACGMNLBLFPQV-UHFFFAOYSA-N 0.000 claims description 5
- LWTBOAFHBJYIAK-UHFFFAOYSA-N 2-[2-(4-methoxyphenyl)ethoxy]-6-piperazin-1-ylpyrazine Chemical compound C1=CC(OC)=CC=C1CCOC1=CN=CC(N2CCNCC2)=N1 LWTBOAFHBJYIAK-UHFFFAOYSA-N 0.000 claims description 5
- PIPQCNRCBHVBNI-UHFFFAOYSA-N 3-[2-(6-piperazin-1-ylpyrazin-2-yl)oxyethyl]-1h-indole Chemical compound C=1NC2=CC=CC=C2C=1CCOC(N=1)=CN=CC=1N1CCNCC1 PIPQCNRCBHVBNI-UHFFFAOYSA-N 0.000 claims description 5
- IIYVNMXPYWIJBL-UHFFFAOYSA-N 4-(trifluoromethyl)pyridine Chemical class FC(F)(F)C1=CC=NC=C1 IIYVNMXPYWIJBL-UHFFFAOYSA-N 0.000 claims description 5
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 5
- XIEQLUARAUTYHZ-UHFFFAOYSA-N n,n-dimethyl-4-[2-(6-piperazin-1-ylpyrazin-2-yl)oxyethyl]aniline Chemical compound C1=CC(N(C)C)=CC=C1CCOC1=CN=CC(N2CCNCC2)=N1 XIEQLUARAUTYHZ-UHFFFAOYSA-N 0.000 claims description 5
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 5
- 230000003287 optical effect Effects 0.000 claims description 5
- 239000000651 prodrug Chemical group 0.000 claims description 5
- 229940002612 prodrug Drugs 0.000 claims description 5
- WLYGONWLTCNUAJ-UHFFFAOYSA-N 1-[2-(6-piperazin-1-ylpyrazin-2-yl)oxyethyl]indole Chemical compound C1=CC2=CC=CC=C2N1CCOC(N=1)=CN=CC=1N1CCNCC1 WLYGONWLTCNUAJ-UHFFFAOYSA-N 0.000 claims description 4
- ONEWTSTYTVDELU-UHFFFAOYSA-N 2-(2-phenylethoxy)-6-piperazin-1-ylpyrazine Chemical compound C=1N=CC(N2CCNCC2)=NC=1OCCC1=CC=CC=C1 ONEWTSTYTVDELU-UHFFFAOYSA-N 0.000 claims description 4
- LGQFYTYRWGWUEY-UHFFFAOYSA-N 2-(2-phenylethylsulfanyl)-6-piperazin-1-ylpyrazine Chemical compound C=1N=CC(N2CCNCC2)=NC=1SCCC1=CC=CC=C1 LGQFYTYRWGWUEY-UHFFFAOYSA-N 0.000 claims description 4
- MCEYUYLACAMCON-UHFFFAOYSA-N 2-(3,4-dihydro-2h-chromen-4-yloxy)-6-piperazin-1-ylpyrazine Chemical compound C1CNCCN1C1=CN=CC(OC2C3=CC=CC=C3OCC2)=N1 MCEYUYLACAMCON-UHFFFAOYSA-N 0.000 claims description 4
- HZNHDQJKDHRQNV-UHFFFAOYSA-N 2-(naphthalen-1-ylmethoxy)-6-piperazin-1-ylpyrazine Chemical compound C=1C=CC2=CC=CC=C2C=1COC(N=1)=CN=CC=1N1CCNCC1 HZNHDQJKDHRQNV-UHFFFAOYSA-N 0.000 claims description 4
- CELNOZABGKVYCG-UHFFFAOYSA-N 2-[(2-chlorophenyl)methylsulfanyl]-6-piperazin-1-ylpyrazine Chemical compound ClC1=CC=CC=C1CSC1=CN=CC(N2CCNCC2)=N1 CELNOZABGKVYCG-UHFFFAOYSA-N 0.000 claims description 4
- HSLQBXHVDRKYOM-CYBMUJFWSA-N 2-[(2r)-2-methylpiperazin-1-yl]-6-phenylmethoxypyrazine Chemical compound C[C@@H]1CNCCN1C1=CN=CC(OCC=2C=CC=CC=2)=N1 HSLQBXHVDRKYOM-CYBMUJFWSA-N 0.000 claims description 4
- FPPQVDJKEFJQSA-UHFFFAOYSA-N 2-[(3,5-difluorophenyl)methoxy]-6-piperazin-1-ylpyrazine Chemical compound FC1=CC(F)=CC(COC=2N=C(C=NC=2)N2CCNCC2)=C1 FPPQVDJKEFJQSA-UHFFFAOYSA-N 0.000 claims description 4
- GMBHDVADYGOKQJ-UHFFFAOYSA-N 2-[(5-fluoro-2-methoxyphenyl)methoxy]-6-piperazin-1-ylpyrazine Chemical compound COC1=CC=C(F)C=C1COC1=CN=CC(N2CCNCC2)=N1 GMBHDVADYGOKQJ-UHFFFAOYSA-N 0.000 claims description 4
- FCVRQVXLAUUCFD-UHFFFAOYSA-N 2-[2-(2-methoxyphenyl)ethoxy]-6-piperazin-1-ylpyrazine Chemical compound COC1=CC=CC=C1CCOC1=CN=CC(N2CCNCC2)=N1 FCVRQVXLAUUCFD-UHFFFAOYSA-N 0.000 claims description 4
- MYBKNHDSVNZGDM-UHFFFAOYSA-N 2-[2-(3-methoxyphenyl)ethoxy]-6-piperazin-1-ylpyrazine Chemical compound COC1=CC=CC(CCOC=2N=C(C=NC=2)N2CCNCC2)=C1 MYBKNHDSVNZGDM-UHFFFAOYSA-N 0.000 claims description 4
- YMGWSIGLNZOGPL-UHFFFAOYSA-N 2-benzyl-6-piperazin-1-ylpyrazine Chemical compound C=1N=CC(N2CCNCC2)=NC=1CC1=CC=CC=C1 YMGWSIGLNZOGPL-UHFFFAOYSA-N 0.000 claims description 4
- OMMBWIWJPLKNFD-UHFFFAOYSA-N 2-phenylmethoxy-6-piperazin-1-ylpyrazine Chemical compound C=1C=CC=CC=1COC(N=1)=CN=CC=1N1CCNCC1 OMMBWIWJPLKNFD-UHFFFAOYSA-N 0.000 claims description 4
- UXJDGSAVALXBTN-UHFFFAOYSA-N 3-[(6-piperazin-1-ylpyrazin-2-yl)oxymethyl]benzonitrile Chemical compound N#CC1=CC=CC(COC=2N=C(C=NC=2)N2CCNCC2)=C1 UXJDGSAVALXBTN-UHFFFAOYSA-N 0.000 claims description 4
- CPVBWHBWLRSCHV-UHFFFAOYSA-N 4-[(2-methoxyphenyl)methoxy]-2-piperazin-1-ylpyrimidine Chemical compound COC1=CC=CC=C1COC1=CC=NC(N2CCNCC2)=N1 CPVBWHBWLRSCHV-UHFFFAOYSA-N 0.000 claims description 4
- 125000004195 4-methylpiperazin-1-yl group Chemical group [H]C([H])([H])N1C([H])([H])C([H])([H])N(*)C([H])([H])C1([H])[H] 0.000 claims description 4
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims description 4
- 125000006314 C5-C8 alkoxy group Chemical group 0.000 claims description 4
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 claims description 4
- 125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 claims description 4
- 125000004216 fluoromethyl group Chemical group [H]C([H])(F)* 0.000 claims description 4
- 238000004519 manufacturing process Methods 0.000 claims description 4
- 125000001424 substituent group Chemical group 0.000 claims description 4
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 claims description 4
- HSLQBXHVDRKYOM-UHFFFAOYSA-N 2-(2-methylpiperazin-1-yl)-6-phenylmethoxypyrazine Chemical compound CC1CNCCN1C1=CN=CC(OCC=2C=CC=CC=2)=N1 HSLQBXHVDRKYOM-UHFFFAOYSA-N 0.000 claims description 3
- KFQAFBLQNMBHQA-UHFFFAOYSA-N 2-(3-naphthalen-2-yloxypropoxy)-6-piperazin-1-ylpyrazine Chemical compound C=1C=C2C=CC=CC2=CC=1OCCCOC(N=1)=CN=CC=1N1CCNCC1 KFQAFBLQNMBHQA-UHFFFAOYSA-N 0.000 claims description 3
- CMKZSOBBCDDCME-UHFFFAOYSA-N 2-(5-phenoxypentoxy)-6-piperazin-1-ylpyrazine Chemical compound C=1N=CC(N2CCNCC2)=NC=1OCCCCCOC1=CC=CC=C1 CMKZSOBBCDDCME-UHFFFAOYSA-N 0.000 claims description 3
- ZQVATTAHFXNGKF-UHFFFAOYSA-N 2-[(2,5-dimethoxyphenyl)methoxy]-6-piperazin-1-ylpyrazine Chemical compound COC1=CC=C(OC)C(COC=2N=C(C=NC=2)N2CCNCC2)=C1 ZQVATTAHFXNGKF-UHFFFAOYSA-N 0.000 claims description 3
- VOWRKUOBQLCBJI-UHFFFAOYSA-N 2-[(2-phenoxyphenyl)methoxy]-6-piperazin-1-ylpyrazine Chemical compound C=1C=CC=C(OC=2C=CC=CC=2)C=1COC(N=1)=CN=CC=1N1CCNCC1 VOWRKUOBQLCBJI-UHFFFAOYSA-N 0.000 claims description 3
- QMMYOJDSVCRMCE-UHFFFAOYSA-N 2-[1-(2,6-difluorophenyl)ethoxy]-6-piperazin-1-ylpyrazine Chemical compound FC=1C=CC=C(F)C=1C(C)OC(N=1)=CN=CC=1N1CCNCC1 QMMYOJDSVCRMCE-UHFFFAOYSA-N 0.000 claims description 3
- LALFVUJPHIMHMK-UHFFFAOYSA-N 2-[2-(2,5-dimethoxyphenyl)ethoxy]-6-piperazin-1-ylpyrazine Chemical compound COC1=CC=C(OC)C(CCOC=2N=C(C=NC=2)N2CCNCC2)=C1 LALFVUJPHIMHMK-UHFFFAOYSA-N 0.000 claims description 3
- WKSVBLNPKMLRHD-UHFFFAOYSA-N 2-[2-(2-fluorophenyl)ethoxy]-6-piperazin-1-ylpyrazine Chemical compound FC1=CC=CC=C1CCOC1=CN=CC(N2CCNCC2)=N1 WKSVBLNPKMLRHD-UHFFFAOYSA-N 0.000 claims description 3
- RQBCVNKTVFSCKQ-UHFFFAOYSA-N 2-[2-(7-methoxynaphthalen-2-yl)oxyethoxy]-6-piperazin-1-ylpyrazine Chemical compound C=1C2=CC(OC)=CC=C2C=CC=1OCCOC(N=1)=CN=CC=1N1CCNCC1 RQBCVNKTVFSCKQ-UHFFFAOYSA-N 0.000 claims description 3
- YYWATUWCINOWOO-UHFFFAOYSA-N 2-[[5-(4-chlorophenyl)-2-methylfuran-3-yl]methoxy]-6-piperazin-1-ylpyrazine Chemical compound CC=1OC(C=2C=CC(Cl)=CC=2)=CC=1COC(N=1)=CN=CC=1N1CCNCC1 YYWATUWCINOWOO-UHFFFAOYSA-N 0.000 claims description 3
- 125000000094 2-phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 claims description 3
- ZZGXJWPNJUVOCQ-UHFFFAOYSA-N 4-phenylmethoxy-2-piperazin-1-ylpyrimidine Chemical compound C=1C=CC=CC=1COC(N=1)=CC=NC=1N1CCNCC1 ZZGXJWPNJUVOCQ-UHFFFAOYSA-N 0.000 claims description 3
- APOVIXFCVJIIQD-UHFFFAOYSA-N 5-methyl-2-phenyl-4-[2-(6-piperazin-1-ylpyrazin-2-yl)oxyethyl]-1,3-oxazole Chemical compound CC=1OC(C=2C=CC=CC=2)=NC=1CCOC(N=1)=CN=CC=1N1CCNCC1 APOVIXFCVJIIQD-UHFFFAOYSA-N 0.000 claims description 3
- KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 claims description 3
- 239000004480 active ingredient Substances 0.000 claims description 3
- 125000003545 alkoxy group Chemical group 0.000 claims description 3
- 150000001408 amides Chemical class 0.000 claims description 3
- 238000011321 prophylaxis Methods 0.000 claims description 3
- 239000012453 solvate Substances 0.000 claims description 3
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 2
- OTBMPVXGHZGFFT-UHFFFAOYSA-N 2-(2,3-dihydro-1h-inden-1-ylmethoxy)-6-piperazin-1-ylpyrazine;2-(4-phenoxybutoxy)-6-piperazin-1-ylpyrazine Chemical compound C1CC2=CC=CC=C2C1COC(N=1)=CN=CC=1N1CCNCC1.C=1C=CC=CC=1OCCCCOC(N=1)=CN=CC=1N1CCNCC1 OTBMPVXGHZGFFT-UHFFFAOYSA-N 0.000 claims description 2
- ZJRXYNVDTHFHHD-UHFFFAOYSA-N 2-(2-naphthalen-2-ylethoxy)-6-piperazin-1-ylpyrazine Chemical compound C=1C=C2C=CC=CC2=CC=1CCOC(N=1)=CN=CC=1N1CCNCC1 ZJRXYNVDTHFHHD-UHFFFAOYSA-N 0.000 claims description 2
- 125000001731 2-cyanoethyl group Chemical group [H]C([H])(*)C([H])([H])C#N 0.000 claims description 2
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 claims description 2
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims description 2
- JDVLFAOIOOISOZ-UHFFFAOYSA-N 4-[(6-piperazin-1-ylpyrazin-2-yl)oxymethyl]-1h-indole Chemical compound C=1C=CC=2NC=CC=2C=1COC(N=1)=CN=CC=1N1CCNCC1 JDVLFAOIOOISOZ-UHFFFAOYSA-N 0.000 claims description 2
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims description 2
- 125000001246 bromo group Chemical group Br* 0.000 claims description 2
- 239000003153 chemical reaction reagent Substances 0.000 claims description 2
- 239000003937 drug carrier Substances 0.000 claims description 2
- 150000004677 hydrates Chemical class 0.000 claims description 2
- 125000003386 piperidinyl group Chemical group 0.000 claims description 2
- BRNULMACUQOKMR-UHFFFAOYSA-N thiomorpholine Chemical compound C1CSCCN1 BRNULMACUQOKMR-UHFFFAOYSA-N 0.000 claims description 2
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 13
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims 3
- 125000000204 (C2-C4) acyl group Chemical group 0.000 claims 2
- KNJBRMFQPLOXRI-UHFFFAOYSA-N 2-(1-benzothiophen-3-ylmethoxy)-6-piperazin-1-ylpyrazine;2-[(2-fluorophenyl)methoxy]-6-piperazin-1-ylpyrazine Chemical compound FC1=CC=CC=C1COC1=CN=CC(N2CCNCC2)=N1.C=1SC2=CC=CC=C2C=1COC(N=1)=CN=CC=1N1CCNCC1 KNJBRMFQPLOXRI-UHFFFAOYSA-N 0.000 claims 1
- QYEQKTXDCDVJEU-DFQHDRSWSA-N 2-[(2S,5R)-2,5-dimethylpiperazin-1-yl]-6-phenylmethoxypyrazine 2-(2-ethylpiperazin-1-yl)-6-phenylmethoxypyrazine Chemical compound C(C1=CC=CC=C1)OC1=CN=CC(=N1)N1[C@H](CN[C@@H](C1)C)C.C(C1=CC=CC=C1)OC1=CN=CC(=N1)N1C(CNCC1)CC QYEQKTXDCDVJEU-DFQHDRSWSA-N 0.000 claims 1
- XDOYAEMEIBUWNM-UHFFFAOYSA-N 2-[(3-phenylmethoxyphenyl)methoxy]-4-piperazin-1-ylpyrimidine Chemical compound C=1C=CC=CC=1COC(C=1)=CC=CC=1COC(N=1)=NC=CC=1N1CCNCC1 XDOYAEMEIBUWNM-UHFFFAOYSA-N 0.000 claims 1
- HNTXLOYVXKWKTN-UHFFFAOYSA-N CC(CC1=CC=CC=C1)OC1=NC(=CN=C1)N1CCNCC1.C1=C(C=CC2=CC=CC=C12)OCCOC1=NC(=CN=C1)N1CCNCC1.FC1=C(OCCOC2=NC(=CN=C2)N2CCNCC2)C(=CC=C1)F Chemical compound CC(CC1=CC=CC=C1)OC1=NC(=CN=C1)N1CCNCC1.C1=C(C=CC2=CC=CC=C12)OCCOC1=NC(=CN=C1)N1CCNCC1.FC1=C(OCCOC2=NC(=CN=C2)N2CCNCC2)C(=CC=C1)F HNTXLOYVXKWKTN-UHFFFAOYSA-N 0.000 claims 1
- VBOPJBDTPSGGJV-UHFFFAOYSA-N FC1=C(COC2=NC(=CN=C2)N2CCNCC2)C=C(C=C1)F.FC=1C=CC(=C(COC2=NC(=CN=C2)N2CCNCC2)C1)OC.O(C1=CC=CC=C1)CC1=C(COC2=NC(=CN=C2)N2CCNCC2)C=CC=C1 Chemical compound FC1=C(COC2=NC(=CN=C2)N2CCNCC2)C=C(C=C1)F.FC=1C=CC(=C(COC2=NC(=CN=C2)N2CCNCC2)C1)OC.O(C1=CC=CC=C1)CC1=C(COC2=NC(=CN=C2)N2CCNCC2)C=CC=C1 VBOPJBDTPSGGJV-UHFFFAOYSA-N 0.000 claims 1
- 150000001204 N-oxides Chemical group 0.000 claims 1
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims 1
- 125000005015 aryl alkynyl group Chemical group 0.000 claims 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 1
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 153
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 105
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 97
- 239000003921 oil Substances 0.000 description 93
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 87
- 239000000203 mixture Substances 0.000 description 80
- 238000004128 high performance liquid chromatography Methods 0.000 description 72
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Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom 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
- C07D213/62—Oxygen or sulfur atoms
- C07D213/63—One oxygen atom
- C07D213/64—One oxygen atom attached in position 2 or 6
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- 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
- C07D401/04—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 directly linked by a ring-member-to-ring-member bond
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/4965—Non-condensed pyrazines
- A61K31/497—Non-condensed pyrazines containing further heterocyclic rings
-
- A—HUMAN NECESSITIES
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| SE0004245A SE0004245D0 (sv) | 2000-11-20 | 2000-11-20 | Novel compounds and their use |
| US25350900P | 2000-11-28 | 2000-11-28 | |
| US60/253,509 | 2000-11-28 | ||
| PCT/SE2001/002569 WO2002040456A1 (en) | 2000-11-20 | 2001-11-20 | Piperazinylpyrazine compounds as agonist or antagonist of serotonin 5ht-2 receptor |
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| CA2448729A1 true CA2448729A1 (en) | 2002-05-23 |
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| CA002448729A Abandoned CA2448729A1 (en) | 2000-11-20 | 2001-11-20 | Piperazinyl and piperidyl substituted heterocyclic compounds |
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| US7226925B2 (en) | 2002-06-19 | 2007-06-05 | Biovitrum Ab | Compounds, their use and preparation |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4954502A (en) * | 1988-06-10 | 1990-09-04 | Bristol-Myers Squibb Company | 1-indolyalkyl-4-(substituted-pyridinyl)piperazines |
| IE911774A1 (en) * | 1990-06-11 | 1991-12-18 | Akzo Nv | Pyridinylpiperazine derivatives |
| US5578596A (en) * | 1992-11-09 | 1996-11-26 | Asahi Kasei Kogyo Kabushiki Kaisha | 2-alkoxy-5,6,7,8-tetrahydroquinoxaline derivatives, and production method and use thereof |
| JPH07300474A (ja) * | 1994-05-02 | 1995-11-14 | Asahi Chem Ind Co Ltd | テトラハイドロキノキサリン誘導体およびその用途 |
| FR2761071B1 (fr) * | 1997-03-20 | 1999-12-03 | Synthelabo | Derives de quinolein-2(1h)-one et de dihydroquinolein-2(1h)- one, leur preparation et leur application en therapeutique |
| GB9718833D0 (en) * | 1997-09-04 | 1997-11-12 | Merck Sharp & Dohme | Therapeutic agents |
| DE69938005T2 (de) * | 1998-09-22 | 2009-01-15 | Astellas Pharma Inc. | Cyanophenyl-derivate |
| FR2788772B1 (fr) * | 1999-01-26 | 2001-03-02 | Adir | Nouveaux composes cyano-indoles inhibiteurs de recapture de serotonine, leur procede de preparation et les compositions pharmaceutiques qui les contiennent |
| HRP20010604A2 (en) * | 1999-02-24 | 2002-08-31 | Hoffmann La Roche | 3-phenylpyridine derivatives and their use as nk-1 receptor antagonists |
-
2001
- 2001-11-20 CA CA002448729A patent/CA2448729A1/en not_active Abandoned
- 2001-11-20 NZ NZ525700A patent/NZ525700A/xx unknown
- 2001-11-20 PL PL01361690A patent/PL361690A1/xx not_active Application Discontinuation
- 2001-11-20 AU AU2426602A patent/AU2426602A/xx active Pending
- 2001-11-20 IL IL15570201A patent/IL155702A0/xx unknown
- 2001-11-20 DE DE60142355T patent/DE60142355D1/de not_active Expired - Lifetime
- 2001-11-20 AT AT01996532T patent/ATE470662T1/de not_active IP Right Cessation
- 2001-11-20 BR BR0115400-1A patent/BR0115400A/pt not_active IP Right Cessation
- 2001-11-20 JP JP2002542784A patent/JP4387103B2/ja not_active Expired - Fee Related
- 2001-11-20 WO PCT/SE2001/002569 patent/WO2002040456A1/en not_active Ceased
- 2001-11-20 CN CNB018204058A patent/CN1267424C/zh not_active Expired - Fee Related
- 2001-11-20 KR KR1020037006824A patent/KR100846339B1/ko not_active Expired - Fee Related
- 2001-11-20 EP EP01996532A patent/EP1335907B1/en not_active Expired - Lifetime
- 2001-11-20 AU AU2002224266A patent/AU2002224266B2/en not_active Ceased
- 2001-11-20 MX MXPA03004390A patent/MXPA03004390A/es active IP Right Grant
-
2003
- 2003-05-01 IL IL155702A patent/IL155702A/en not_active IP Right Cessation
- 2003-05-19 NO NO20032252A patent/NO325181B1/no not_active IP Right Cessation
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2009
- 2009-06-23 JP JP2009148822A patent/JP2009280587A/ja active Pending
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|---|---|
| AU2002224266B2 (en) | 2007-05-24 |
| NO20032252D0 (no) | 2003-05-19 |
| KR20030060947A (ko) | 2003-07-16 |
| HK1061855A1 (en) | 2004-10-08 |
| AU2426602A (en) | 2002-05-27 |
| EP1335907B1 (en) | 2010-06-09 |
| CN1267424C (zh) | 2006-08-02 |
| NO325181B1 (no) | 2008-02-11 |
| JP4387103B2 (ja) | 2009-12-16 |
| ATE470662T1 (de) | 2010-06-15 |
| PL361690A1 (en) | 2004-10-04 |
| BR0115400A (pt) | 2003-09-30 |
| DE60142355D1 (de) | 2010-07-22 |
| EP1335907A1 (en) | 2003-08-20 |
| KR100846339B1 (ko) | 2008-07-15 |
| JP2009280587A (ja) | 2009-12-03 |
| IL155702A0 (en) | 2003-11-23 |
| NO20032252L (no) | 2003-07-18 |
| IL155702A (en) | 2010-05-31 |
| WO2002040456A1 (en) | 2002-05-23 |
| CN1479727A (zh) | 2004-03-03 |
| HK1099292A1 (zh) | 2007-08-10 |
| MXPA03004390A (es) | 2004-05-14 |
| NZ525700A (en) | 2004-12-24 |
| JP2004532806A (ja) | 2004-10-28 |
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