KR880000410A - 이치환된 피페라진 - Google Patents
이치환된 피페라진 Download PDFInfo
- Publication number
- KR880000410A KR880000410A KR1019870006034A KR870006034A KR880000410A KR 880000410 A KR880000410 A KR 880000410A KR 1019870006034 A KR1019870006034 A KR 1019870006034A KR 870006034 A KR870006034 A KR 870006034A KR 880000410 A KR880000410 A KR 880000410A
- Authority
- KR
- South Korea
- Prior art keywords
- piperazine
- ethyl
- chlorophenyl
- compound
- salt
- 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.)
- Ceased
Links
- 150000004885 piperazines Chemical class 0.000 title 1
- 150000003839 salts Chemical class 0.000 claims 33
- 150000001875 compounds Chemical class 0.000 claims 32
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 16
- 238000000034 method Methods 0.000 claims 12
- -1 C 1 -C 7 -alkoxy Chemical group 0.000 claims 11
- 229910052736 halogen Inorganic materials 0.000 claims 9
- 150000002367 halogens Chemical class 0.000 claims 9
- 125000001255 4-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1F 0.000 claims 7
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 claims 7
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 5
- 229910052801 chlorine Inorganic materials 0.000 claims 5
- 239000000460 chlorine Substances 0.000 claims 5
- 229910052731 fluorine Inorganic materials 0.000 claims 5
- 239000011737 fluorine Substances 0.000 claims 5
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 5
- 125000004198 2-fluorophenyl group Chemical group [H]C1=C([H])C(F)=C(*)C([H])=C1[H] 0.000 claims 3
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 3
- 239000008194 pharmaceutical composition Substances 0.000 claims 3
- 238000002360 preparation method Methods 0.000 claims 3
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 2
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 claims 2
- KQHKRRSQPGNZBU-UHFFFAOYSA-N [4-[2-(4-chlorophenyl)ethyl]piperazin-1-yl]-(2-fluorophenyl)methanone Chemical compound FC1=CC=CC=C1C(=O)N1CCN(CCC=2C=CC(Cl)=CC=2)CC1 KQHKRRSQPGNZBU-UHFFFAOYSA-N 0.000 claims 2
- IPBRFUZGLJYPAG-UHFFFAOYSA-N [4-[2-(4-chlorophenyl)ethyl]piperazin-1-yl]-(4-methylphenyl)methanone Chemical compound C1=CC(C)=CC=C1C(=O)N1CCN(CCC=2C=CC(Cl)=CC=2)CC1 IPBRFUZGLJYPAG-UHFFFAOYSA-N 0.000 claims 2
- 229940035676 analgesics Drugs 0.000 claims 2
- 239000000730 antalgic agent Substances 0.000 claims 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 2
- 125000001153 fluoro group Chemical group F* 0.000 claims 2
- 229910052739 hydrogen Inorganic materials 0.000 claims 2
- 239000001257 hydrogen Substances 0.000 claims 2
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims 2
- FNGMUJOECSGYTE-UHFFFAOYSA-N (2-aminophenyl)-[4-(2-phenylethyl)piperazin-1-yl]methanone Chemical compound NC1=CC=CC=C1C(=O)N1CCN(CCC=2C=CC=CC=2)CC1 FNGMUJOECSGYTE-UHFFFAOYSA-N 0.000 claims 1
- SDRIGNBTIPFMOU-UHFFFAOYSA-N (2-aminophenyl)-[4-[2-(4-chlorophenyl)ethyl]piperazin-1-yl]methanone Chemical compound NC1=CC=CC=C1C(=O)N1CCN(CCC=2C=CC(Cl)=CC=2)CC1 SDRIGNBTIPFMOU-UHFFFAOYSA-N 0.000 claims 1
- MXRGJBQXGSTMQL-UHFFFAOYSA-N (2-chlorophenyl)-[4-[2-(4-chlorophenyl)ethyl]piperazin-1-yl]methanone Chemical compound C1=CC(Cl)=CC=C1CCN1CCN(C(=O)C=2C(=CC=CC=2)Cl)CC1 MXRGJBQXGSTMQL-UHFFFAOYSA-N 0.000 claims 1
- UPWQKCPUOBLXET-UHFFFAOYSA-N (3,4-dimethoxyphenyl)-[4-(2-phenylethyl)piperazin-1-yl]methanone Chemical compound C1=C(OC)C(OC)=CC=C1C(=O)N1CCN(CCC=2C=CC=CC=2)CC1 UPWQKCPUOBLXET-UHFFFAOYSA-N 0.000 claims 1
- LVQXLRHYRDUDGT-UHFFFAOYSA-N (3,4-dimethoxyphenyl)-[4-[2-(4-fluorophenyl)ethyl]piperazin-1-yl]methanone Chemical compound C1=C(OC)C(OC)=CC=C1C(=O)N1CCN(CCC=2C=CC(F)=CC=2)CC1 LVQXLRHYRDUDGT-UHFFFAOYSA-N 0.000 claims 1
- MJYVFJZCIJVOIR-UHFFFAOYSA-N (3,4-dimethoxyphenyl)-[4-[2-(4-methoxyphenyl)ethyl]piperazin-1-yl]methanone Chemical compound C1=CC(OC)=CC=C1CCN1CCN(C(=O)C=2C=C(OC)C(OC)=CC=2)CC1 MJYVFJZCIJVOIR-UHFFFAOYSA-N 0.000 claims 1
- MWWDHIIGTNYFIC-UHFFFAOYSA-N (3-chlorophenyl)-[4-[2-(4-chlorophenyl)ethyl]piperazin-1-yl]methanone Chemical compound C1=CC(Cl)=CC=C1CCN1CCN(C(=O)C=2C=C(Cl)C=CC=2)CC1 MWWDHIIGTNYFIC-UHFFFAOYSA-N 0.000 claims 1
- ZUPJTGGTBHOUFJ-UHFFFAOYSA-N (3-methoxyphenyl)-[4-(2-phenylethyl)piperazin-1-yl]methanone Chemical compound COC1=CC=CC(C(=O)N2CCN(CCC=3C=CC=CC=3)CC2)=C1 ZUPJTGGTBHOUFJ-UHFFFAOYSA-N 0.000 claims 1
- ZSBOQEHCUSDKIK-UHFFFAOYSA-N (3-methoxyphenyl)-[4-[2-(4-methoxyphenyl)ethyl]piperazin-1-yl]methanone Chemical compound C1=CC(OC)=CC=C1CCN1CCN(C(=O)C=2C=C(OC)C=CC=2)CC1 ZSBOQEHCUSDKIK-UHFFFAOYSA-N 0.000 claims 1
- USFHSUPDJPHDCH-UHFFFAOYSA-N (4-chlorophenyl)-[4-[2-(4-chlorophenyl)ethyl]piperazin-1-yl]methanone Chemical compound C1=CC(Cl)=CC=C1CCN1CCN(C(=O)C=2C=CC(Cl)=CC=2)CC1 USFHSUPDJPHDCH-UHFFFAOYSA-N 0.000 claims 1
- GWKFJCLHSBNKRR-UHFFFAOYSA-N (4-chlorophenyl)-[4-[2-(4-fluorophenyl)ethyl]piperazin-1-yl]methanone Chemical compound C1=CC(F)=CC=C1CCN1CCN(C(=O)C=2C=CC(Cl)=CC=2)CC1 GWKFJCLHSBNKRR-UHFFFAOYSA-N 0.000 claims 1
- XAWLTTKNJJTQOP-UHFFFAOYSA-N (4-fluorophenyl)-[4-[2-(4-fluorophenyl)ethyl]piperazin-1-yl]methanone Chemical compound C1=CC(F)=CC=C1CCN1CCN(C(=O)C=2C=CC(F)=CC=2)CC1 XAWLTTKNJJTQOP-UHFFFAOYSA-N 0.000 claims 1
- 125000004182 2-chlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(*)C([H])=C1[H] 0.000 claims 1
- GVHPAKKEBOAGEO-UHFFFAOYSA-N 3-[4-[2-(4-chlorophenyl)ethyl]piperazine-1-carbonyl]-4-methoxybenzonitrile Chemical compound COC1=CC=C(C#N)C=C1C(=O)N1CCN(CCC=2C=CC(Cl)=CC=2)CC1 GVHPAKKEBOAGEO-UHFFFAOYSA-N 0.000 claims 1
- OKQCKIJAEKZGKF-UHFFFAOYSA-N [4-[2-(3-chlorophenyl)ethyl]piperazin-1-yl]-(3,4-dimethoxyphenyl)methanone Chemical compound C1=C(OC)C(OC)=CC=C1C(=O)N1CCN(CCC=2C=C(Cl)C=CC=2)CC1 OKQCKIJAEKZGKF-UHFFFAOYSA-N 0.000 claims 1
- JBZZYVLHSABMRQ-UHFFFAOYSA-N [4-[2-(3-chlorophenyl)ethyl]piperazin-1-yl]-(3-methoxyphenyl)methanone Chemical compound COC1=CC=CC(C(=O)N2CCN(CCC=3C=C(Cl)C=CC=3)CC2)=C1 JBZZYVLHSABMRQ-UHFFFAOYSA-N 0.000 claims 1
- LVVOLXVLYBAVSN-UHFFFAOYSA-N [4-[2-(4-chlorophenyl)ethyl]piperazin-1-yl]-(2,4-dichlorophenyl)methanone Chemical compound C1=CC(Cl)=CC=C1CCN1CCN(C(=O)C=2C(=CC(Cl)=CC=2)Cl)CC1 LVVOLXVLYBAVSN-UHFFFAOYSA-N 0.000 claims 1
- BPBPJJOOTVZZFA-UHFFFAOYSA-N [4-[2-(4-chlorophenyl)ethyl]piperazin-1-yl]-(2,6-dichlorophenyl)methanone Chemical compound C1=CC(Cl)=CC=C1CCN1CCN(C(=O)C=2C(=CC=CC=2Cl)Cl)CC1 BPBPJJOOTVZZFA-UHFFFAOYSA-N 0.000 claims 1
- WMZAGDKSMHFPIX-UHFFFAOYSA-N [4-[2-(4-chlorophenyl)ethyl]piperazin-1-yl]-(2,6-dimethoxyphenyl)methanone Chemical compound COC1=CC=CC(OC)=C1C(=O)N1CCN(CCC=2C=CC(Cl)=CC=2)CC1 WMZAGDKSMHFPIX-UHFFFAOYSA-N 0.000 claims 1
- ZYAAYACQKSMOSR-UHFFFAOYSA-N [4-[2-(4-chlorophenyl)ethyl]piperazin-1-yl]-(2,6-dimethylphenyl)methanone Chemical compound CC1=CC=CC(C)=C1C(=O)N1CCN(CCC=2C=CC(Cl)=CC=2)CC1 ZYAAYACQKSMOSR-UHFFFAOYSA-N 0.000 claims 1
- UZBMPRCGMGQYOA-UHFFFAOYSA-N [4-[2-(4-chlorophenyl)ethyl]piperazin-1-yl]-(2-methoxyphenyl)methanone Chemical compound COC1=CC=CC=C1C(=O)N1CCN(CCC=2C=CC(Cl)=CC=2)CC1 UZBMPRCGMGQYOA-UHFFFAOYSA-N 0.000 claims 1
- OGVVWKXFDLLJGT-UHFFFAOYSA-N [4-[2-(4-chlorophenyl)ethyl]piperazin-1-yl]-(2-methylphenyl)methanone Chemical compound CC1=CC=CC=C1C(=O)N1CCN(CCC=2C=CC(Cl)=CC=2)CC1 OGVVWKXFDLLJGT-UHFFFAOYSA-N 0.000 claims 1
- IRYLTVZJXAKIAZ-UHFFFAOYSA-N [4-[2-(4-chlorophenyl)ethyl]piperazin-1-yl]-(3,4-dichlorophenyl)methanone Chemical compound C1=CC(Cl)=CC=C1CCN1CCN(C(=O)C=2C=C(Cl)C(Cl)=CC=2)CC1 IRYLTVZJXAKIAZ-UHFFFAOYSA-N 0.000 claims 1
- JRZOORQRAQDSNQ-UHFFFAOYSA-N [4-[2-(4-chlorophenyl)ethyl]piperazin-1-yl]-(3,4-dimethoxyphenyl)methanone Chemical compound C1=C(OC)C(OC)=CC=C1C(=O)N1CCN(CCC=2C=CC(Cl)=CC=2)CC1 JRZOORQRAQDSNQ-UHFFFAOYSA-N 0.000 claims 1
- FWKINTJJDACZMR-UHFFFAOYSA-N [4-[2-(4-chlorophenyl)ethyl]piperazin-1-yl]-(3,5-dichlorophenyl)methanone Chemical compound C1=CC(Cl)=CC=C1CCN1CCN(C(=O)C=2C=C(Cl)C=C(Cl)C=2)CC1 FWKINTJJDACZMR-UHFFFAOYSA-N 0.000 claims 1
- ORGYHESNXRTMRD-UHFFFAOYSA-N [4-[2-(4-chlorophenyl)ethyl]piperazin-1-yl]-(3-fluorophenyl)methanone Chemical compound FC1=CC=CC(C(=O)N2CCN(CCC=3C=CC(Cl)=CC=3)CC2)=C1 ORGYHESNXRTMRD-UHFFFAOYSA-N 0.000 claims 1
- ITRWZFVGJDQZIU-UHFFFAOYSA-N [4-[2-(4-chlorophenyl)ethyl]piperazin-1-yl]-(3-methoxyphenyl)methanone Chemical compound COC1=CC=CC(C(=O)N2CCN(CCC=3C=CC(Cl)=CC=3)CC2)=C1 ITRWZFVGJDQZIU-UHFFFAOYSA-N 0.000 claims 1
- KHUTULPFVBWZME-UHFFFAOYSA-N [4-[2-(4-chlorophenyl)ethyl]piperazin-1-yl]-(4-fluorophenyl)methanone Chemical compound C1=CC(F)=CC=C1C(=O)N1CCN(CCC=2C=CC(Cl)=CC=2)CC1 KHUTULPFVBWZME-UHFFFAOYSA-N 0.000 claims 1
- CJZHOJARNOFKGY-UHFFFAOYSA-N [4-[2-(4-chlorophenyl)ethyl]piperazin-1-yl]-(4-methoxyphenyl)methanone Chemical compound C1=CC(OC)=CC=C1C(=O)N1CCN(CCC=2C=CC(Cl)=CC=2)CC1 CJZHOJARNOFKGY-UHFFFAOYSA-N 0.000 claims 1
- IQPKECPHJLHEEZ-UHFFFAOYSA-N [4-[2-(4-chlorophenyl)ethyl]piperazin-1-yl]-[2-(trifluoromethyl)phenyl]methanone Chemical compound FC(F)(F)C1=CC=CC=C1C(=O)N1CCN(CCC=2C=CC(Cl)=CC=2)CC1 IQPKECPHJLHEEZ-UHFFFAOYSA-N 0.000 claims 1
- SZFKPJVKDMGYOG-UHFFFAOYSA-N [4-[2-(4-chlorophenyl)ethyl]piperazin-1-yl]-[3-(dimethylamino)phenyl]methanone Chemical compound CN(C)C1=CC=CC(C(=O)N2CCN(CCC=3C=CC(Cl)=CC=3)CC2)=C1 SZFKPJVKDMGYOG-UHFFFAOYSA-N 0.000 claims 1
- VKKIECYNIHDSNY-UHFFFAOYSA-N [4-[2-(4-chlorophenyl)ethyl]piperazin-1-yl]-[3-(trifluoromethyl)phenyl]methanone Chemical compound FC(F)(F)C1=CC=CC(C(=O)N2CCN(CCC=3C=CC(Cl)=CC=3)CC2)=C1 VKKIECYNIHDSNY-UHFFFAOYSA-N 0.000 claims 1
- XTQLJIHMIOXTMS-UHFFFAOYSA-N [4-[2-(4-chlorophenyl)ethyl]piperazin-1-yl]-[4-(dimethylamino)phenyl]methanone Chemical compound C1=CC(N(C)C)=CC=C1C(=O)N1CCN(CCC=2C=CC(Cl)=CC=2)CC1 XTQLJIHMIOXTMS-UHFFFAOYSA-N 0.000 claims 1
- OIYJPDQQWCNLFV-UHFFFAOYSA-N [4-[2-(4-chlorophenyl)ethyl]piperazin-1-yl]-[4-(trifluoromethyl)phenyl]methanone Chemical compound C1=CC(C(F)(F)F)=CC=C1C(=O)N1CCN(CCC=2C=CC(Cl)=CC=2)CC1 OIYJPDQQWCNLFV-UHFFFAOYSA-N 0.000 claims 1
- GSIMEYHPNMLREA-UHFFFAOYSA-N [4-[2-(4-fluorophenyl)ethyl]piperazin-1-yl]-(3-methoxyphenyl)methanone Chemical compound COC1=CC=CC(C(=O)N2CCN(CCC=3C=CC(F)=CC=3)CC2)=C1 GSIMEYHPNMLREA-UHFFFAOYSA-N 0.000 claims 1
- 125000000217 alkyl group Chemical group 0.000 claims 1
- 125000004429 atom Chemical group 0.000 claims 1
- 239000000969 carrier Substances 0.000 claims 1
- MXOAEAUPQDYUQM-UHFFFAOYSA-N chlorphenesin Chemical group OCC(O)COC1=CC=C(Cl)C=C1 MXOAEAUPQDYUQM-UHFFFAOYSA-N 0.000 claims 1
- 238000009833 condensation Methods 0.000 claims 1
- 230000005494 condensation Effects 0.000 claims 1
- 125000004093 cyano group Chemical group *C#N 0.000 claims 1
- 125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 claims 1
- 125000000623 heterocyclic group Chemical group 0.000 claims 1
- XMSZANIMCDLNKA-UHFFFAOYSA-N methyl hypofluorite Chemical group COF XMSZANIMCDLNKA-UHFFFAOYSA-N 0.000 claims 1
- 239000000203 mixture Substances 0.000 claims 1
- AOYABYIIPZVRPC-UHFFFAOYSA-N n-[4-[4-[2-(4-chlorophenyl)ethyl]piperazine-1-carbonyl]phenyl]acetamide Chemical compound C1=CC(NC(=O)C)=CC=C1C(=O)N1CCN(CCC=2C=CC(Cl)=CC=2)CC1 AOYABYIIPZVRPC-UHFFFAOYSA-N 0.000 claims 1
- 125000003261 o-tolyl group Chemical group [H]C1=C([H])C(*)=C(C([H])=C1[H])C([H])([H])[H] 0.000 claims 1
- 230000001590 oxidative effect Effects 0.000 claims 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 1
- 239000007858 starting material Substances 0.000 claims 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D241/00—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings
- C07D241/02—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings
- C07D241/10—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
- C07D241/14—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having three 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
- C07D241/18—Oxygen or sulfur atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—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
- 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
- C07D295/182—Radicals derived from carboxylic acids
- C07D295/192—Radicals derived from carboxylic acids from aromatic carboxylic acids
-
- 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
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/06—Antimigraine agents
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—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
- C07D295/04—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 with substituted hydrocarbon radicals attached to ring nitrogen atoms
- C07D295/06—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 with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by halogen atoms or nitro radicals
- C07D295/073—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 with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by halogen atoms or nitro radicals with the ring nitrogen atoms and the substituents separated by carbocyclic rings or by carbon chains interrupted by carbocyclic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—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
- C07D295/04—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 with substituted hydrocarbon radicals attached to ring nitrogen atoms
- C07D295/08—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 with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly bound oxygen or sulfur atoms
- C07D295/096—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 with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly bound oxygen or sulfur atoms with the ring nitrogen atoms and the oxygen or sulfur atoms separated by carbocyclic rings or by carbon chains interrupted by carbocyclic rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Pain & Pain Management (AREA)
- Animal Behavior & Ethology (AREA)
- Engineering & Computer Science (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)
- Lubricants (AREA)
- Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Plural Heterocyclic Compounds (AREA)
- Hydrogenated Pyridines (AREA)
- Removal Of Specific Substances (AREA)
- Water Treatment By Sorption (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH02420/86-2 | 1986-06-16 | ||
| CH242086 | 1986-06-16 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| KR880000410A true KR880000410A (ko) | 1988-03-25 |
Family
ID=4233392
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1019870006034A Ceased KR880000410A (ko) | 1986-06-16 | 1987-06-15 | 이치환된 피페라진 |
Country Status (20)
| Country | Link |
|---|---|
| US (1) | US4804661A (enExample) |
| EP (1) | EP0250361B1 (enExample) |
| JP (1) | JPS62298580A (enExample) |
| KR (1) | KR880000410A (enExample) |
| AT (1) | ATE98237T1 (enExample) |
| AU (1) | AU603584B2 (enExample) |
| DD (1) | DD263289A5 (enExample) |
| DE (1) | DE3788373D1 (enExample) |
| DK (1) | DK167187B1 (enExample) |
| ES (1) | ES2060607T3 (enExample) |
| FI (1) | FI86545C (enExample) |
| HU (1) | HU202508B (enExample) |
| IE (1) | IE61477B1 (enExample) |
| IL (1) | IL82817A0 (enExample) |
| MX (1) | MX6924A (enExample) |
| MY (1) | MY102447A (enExample) |
| NO (1) | NO169961C (enExample) |
| PH (1) | PH23350A (enExample) |
| PT (1) | PT85079B (enExample) |
| ZA (1) | ZA874278B (enExample) |
Families Citing this family (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR910006138B1 (ko) * | 1986-09-30 | 1991-08-16 | 에자이 가부시끼가이샤 | 환상아민 유도체 |
| IL85700A0 (en) * | 1987-03-24 | 1988-08-31 | Takeda Chemical Industries Ltd | 1,4-disubstituted piperazine compounds,their production and use |
| EP0385043A1 (en) * | 1989-02-28 | 1990-09-05 | Fabrica Espanola De Productos Quimicos Y Farmaceuticos, S.A. (Faes) | New derivatives of 4-substituted piperazines |
| EP0489690A1 (de) * | 1990-12-05 | 1992-06-10 | Ciba-Geigy Ag | Substituierte N-Benzoyl-N'-(2-phenylethyl)-piperazine |
| EP0524146A1 (de) * | 1991-07-19 | 1993-01-20 | Ciba-Geigy Ag | Aminosubstituierte Piperazinderivate |
| US5387595A (en) * | 1992-08-26 | 1995-02-07 | Merck & Co., Inc. | Alicyclic compounds as tachykinin receptor antagonists |
| US5344830A (en) * | 1992-12-10 | 1994-09-06 | Merck & Co., Inc. | N,N-diacylpiperazine tachykinin antagonists |
| US5384319A (en) * | 1993-01-06 | 1995-01-24 | Ciba-Geigy Corporation | Aminoalkylphenyl compounds |
| US5380726A (en) * | 1993-01-15 | 1995-01-10 | Ciba-Geigy Corporation | Substituted dialkylthio ethers |
| US5610165A (en) * | 1994-02-17 | 1997-03-11 | Merck & Co., Inc. | N-acylpiperidine tachykinin antagonists |
| JP6486198B2 (ja) * | 2015-05-27 | 2019-03-20 | 国立大学法人 宮崎大学 | アンチモンイオンの抽出剤及びアンチモンイオンの回収方法 |
| EP4452941A1 (de) * | 2021-12-23 | 2024-10-30 | Symrise AG | Wirkstoffe mit mundwässerndem und kribbelndem/prickelndem effekt und zubereitungen, die diese enthalten |
Family Cites Families (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL105768C (enExample) * | 1959-02-25 | |||
| US3000892A (en) * | 1959-11-16 | 1961-09-19 | Paul A J Janssen | 1-aroylalkyl-4-aroylpiperazines |
| FR7170M (enExample) * | 1966-12-28 | 1969-08-11 | ||
| CH590262A5 (enExample) * | 1973-07-10 | 1977-07-29 | Ciba Geigy Ag | |
| US3917617A (en) * | 1973-10-01 | 1975-11-04 | Sharps Ass | 1-{8 2,6-Dihydroxy-4-hydrocarbyl-benzoyl{9 polymethyleneimines and derivatives |
| JPS50151885A (enExample) * | 1974-05-29 | 1975-12-06 | ||
| CY1344A (en) * | 1978-08-10 | 1987-01-16 | Ciba Geigy Ag | Substituted anthranilic acid amides,process for their preparation,and pharmaceutical compositions containing them |
| US4492698A (en) * | 1980-06-16 | 1985-01-08 | Bjoerk Anders K | Diphenylbutyl-1-acylpiperazines |
| FR2522325B1 (fr) * | 1982-02-26 | 1985-08-09 | Delalande Sa | Nouveaux derives aryliques de la piperazine, de l'homopiperazine et de n,n'-dialkyl diamino-1,2 ethane, leur procede de preparation et leur application en therapeutique |
| AU545463B2 (en) * | 1982-06-25 | 1985-07-18 | Kowa Co. Ltd. | Benzoyl piperacine esters |
| IT1176613B (it) * | 1984-08-14 | 1987-08-18 | Ravizza Spa | Derivati piperazinici farmacologicamente attivi e processo per la loro preparazione |
| KR910006138B1 (ko) * | 1986-09-30 | 1991-08-16 | 에자이 가부시끼가이샤 | 환상아민 유도체 |
| IL85700A0 (en) * | 1987-03-24 | 1988-08-31 | Takeda Chemical Industries Ltd | 1,4-disubstituted piperazine compounds,their production and use |
-
1987
- 1987-05-26 MY MYPI87000720A patent/MY102447A/en unknown
- 1987-06-09 IL IL82817A patent/IL82817A0/xx not_active IP Right Cessation
- 1987-06-09 US US07/059,898 patent/US4804661A/en not_active Expired - Fee Related
- 1987-06-10 ES ES87810331T patent/ES2060607T3/es not_active Expired - Lifetime
- 1987-06-10 EP EP87810331A patent/EP0250361B1/de not_active Expired - Lifetime
- 1987-06-10 DE DE87810331T patent/DE3788373D1/de not_active Expired - Fee Related
- 1987-06-10 AT AT87810331T patent/ATE98237T1/de not_active IP Right Cessation
- 1987-06-12 MX MX692487A patent/MX6924A/es unknown
- 1987-06-12 FI FI872637A patent/FI86545C/fi not_active IP Right Cessation
- 1987-06-15 JP JP62147163A patent/JPS62298580A/ja active Granted
- 1987-06-15 KR KR1019870006034A patent/KR880000410A/ko not_active Ceased
- 1987-06-15 DK DK303387A patent/DK167187B1/da not_active Application Discontinuation
- 1987-06-15 PT PT85079A patent/PT85079B/pt not_active IP Right Cessation
- 1987-06-15 DD DD87303827A patent/DD263289A5/de not_active IP Right Cessation
- 1987-06-15 HU HU872710A patent/HU202508B/hu not_active IP Right Cessation
- 1987-06-15 IE IE158287A patent/IE61477B1/en not_active IP Right Cessation
- 1987-06-15 AU AU74219/87A patent/AU603584B2/en not_active Ceased
- 1987-06-15 PH PH35398A patent/PH23350A/en unknown
- 1987-06-15 NO NO872480A patent/NO169961C/no unknown
- 1987-06-15 ZA ZA874278A patent/ZA874278B/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| AU603584B2 (en) | 1990-11-22 |
| FI86545B (fi) | 1992-05-29 |
| FI86545C (fi) | 1992-09-10 |
| PH23350A (en) | 1989-07-14 |
| FI872637A0 (fi) | 1987-06-12 |
| MY102447A (en) | 1992-06-30 |
| NO169961C (no) | 1992-08-26 |
| DK303387A (da) | 1987-12-17 |
| PT85079A (en) | 1987-07-01 |
| ES2060607T3 (es) | 1994-12-01 |
| DD263289A5 (de) | 1988-12-28 |
| DK167187B1 (da) | 1993-09-13 |
| IE61477B1 (en) | 1994-11-02 |
| NO872480D0 (no) | 1987-06-15 |
| NO872480L (no) | 1987-12-17 |
| EP0250361B1 (de) | 1993-12-08 |
| MX6924A (es) | 1993-12-01 |
| ZA874278B (en) | 1987-12-15 |
| HU202508B (en) | 1991-03-28 |
| IE871582L (en) | 1987-12-16 |
| HUT44529A (en) | 1988-03-28 |
| FI872637L (fi) | 1987-12-17 |
| AU7421987A (en) | 1987-12-17 |
| ATE98237T1 (de) | 1993-12-15 |
| US4804661A (en) | 1989-02-14 |
| DE3788373D1 (de) | 1994-01-20 |
| IL82817A0 (en) | 1987-12-20 |
| PT85079B (pt) | 1990-03-08 |
| JPH0579065B2 (enExample) | 1993-11-01 |
| NO169961B (no) | 1992-05-18 |
| EP0250361A3 (en) | 1990-01-31 |
| EP0250361A2 (de) | 1987-12-23 |
| JPS62298580A (ja) | 1987-12-25 |
| DK303387D0 (da) | 1987-06-15 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| EP0288563B1 (en) | Cyclic amine derivatives | |
| KR930700446A (ko) | 하이드록시 및 알콕시 피리딘의 유도체 | |
| DE3566251D1 (en) | Novel intermediate and method for its preparation | |
| RU2001125893A (ru) | Производные 3-фенилпиридина и их применение в качестве антагонистов рецептора NK-1 | |
| KR930005992A (ko) | 루코트리엔 생합성 억제제 | |
| CA2088835A1 (en) | Pyrazole derivatives, processes for preparation thereof and pharmaceutical composition comprising the same | |
| ATE244220T1 (de) | Neue heterocyclische verbindungen, verfahren zu deren herstellung sowie medizinische verwendung | |
| WO2004020430A3 (fr) | Derives de dioxane-2-alkylcarbamates, leur preparation et leur application en therapeutique | |
| ATE147071T1 (de) | 1,4-disubstituierte piperidinderivate, ihre herstellung und therapeutische verwendung | |
| GB2158065A (en) | Dihydropyridines | |
| DK225081A (da) | Aminopropiophenon-derivater og deres syreadditionssalte fremgangsmaader til deres fremstilling og deres anvendelse som gungicider | |
| US4521535A (en) | 4-Pyridone-3-carboxylic acid derivatives | |
| KR950032147A (ko) | 아실화된 아미노알칸이미다졸 및 -트리아졸 | |
| DK0470686T3 (da) | (Benzhydryloxyethylpiperidyl)alifatiske syrederivater og deres anvendelse til behandling af allergier og astma | |
| CA1131641A (en) | Piperazinyl-tetrahydronaphthalene derivatives | |
| US4440771A (en) | 2-Acetyl quinoline thiosemicarbazones useful in treatment of gonorrhea, malaria or bacterial infections | |
| RU2384565C2 (ru) | Фенильные производные, содержащие ацетиленовую группу | |
| HRP20120833T1 (hr) | Derivati benzilpiperazina, korisni u lijeäśenju gastrointestinalnih poremeä†aja | |
| KR890005067A (ko) | 이치환된 피페라진 | |
| KR20150046456A (ko) | 신규한 항진균성 옥소다이하이드로피리딘카보하이드라자이드 유도체 | |
| RU2004126861A (ru) | Производные пиридинамидов в качестве ингибиторов моноаминоксидазы (мао-в) | |
| KR970006305A (ko) | 엔도테린 수용체 길항제 | |
| MX173324B (es) | Procedimiento para la preparacion de nuevas butenamidas farmaceuticas y compuestos relacionados | |
| ATE50248T1 (de) | Ein imidazolidintrion-derivat oder ein seiner pharmazeutisch akzeptierbaren salze enthaltende pharmazeutische zusammenstellung. | |
| NZ331124A (en) | 4-(benzo-1, 3-dioxolyl)-pyrrolidine-3-carboxylic acid derivatives as endothelin antagonists |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PA0109 | Patent application |
Patent event code: PA01091R01D Comment text: Patent Application Patent event date: 19870615 |
|
| PG1501 | Laying open of application | ||
| A201 | Request for examination | ||
| PA0201 | Request for examination |
Patent event code: PA02012R01D Patent event date: 19920615 Comment text: Request for Examination of Application Patent event code: PA02011R01I Patent event date: 19870615 Comment text: Patent Application |
|
| E902 | Notification of reason for refusal | ||
| PE0902 | Notice of grounds for rejection |
Comment text: Notification of reason for refusal Patent event date: 19950425 Patent event code: PE09021S01D |
|
| E601 | Decision to refuse application | ||
| PE0601 | Decision on rejection of patent |
Patent event date: 19950713 Comment text: Decision to Refuse Application Patent event code: PE06012S01D Patent event date: 19950425 Comment text: Notification of reason for refusal Patent event code: PE06011S01I |