NO121663B - - Google Patents
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- Publication number
- NO121663B NO121663B NO166014A NO16601466A NO121663B NO 121663 B NO121663 B NO 121663B NO 166014 A NO166014 A NO 166014A NO 16601466 A NO16601466 A NO 16601466A NO 121663 B NO121663 B NO 121663B
- Authority
- NO
- Norway
- Prior art keywords
- piperazine
- radical
- general formula
- propyl
- melts
- Prior art date
Links
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 7
- 150000003839 salts Chemical class 0.000 claims description 7
- -1 N-mono-substituted piperazine Chemical class 0.000 claims description 6
- 238000000034 method Methods 0.000 claims description 6
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 4
- 125000005843 halogen group Chemical group 0.000 claims description 3
- 150000004885 piperazines Chemical class 0.000 claims description 3
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 2
- 125000004663 dialkyl amino group Chemical group 0.000 claims description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 claims description 2
- 239000011707 mineral Substances 0.000 claims description 2
- 150000007524 organic acids Chemical class 0.000 claims description 2
- 235000005985 organic acids Nutrition 0.000 claims description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 2
- 125000004193 piperazinyl group Chemical group 0.000 claims description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 1
- MDFFNEOEWAXZRQ-UHFFFAOYSA-N aminyl Chemical compound [NH2] MDFFNEOEWAXZRQ-UHFFFAOYSA-N 0.000 claims 1
- 150000007522 mineralic acids Chemical class 0.000 claims 1
- 239000000155 melt Substances 0.000 description 21
- 239000002253 acid Substances 0.000 description 8
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 6
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 description 6
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 6
- 150000007513 acids Chemical class 0.000 description 5
- 238000000354 decomposition reaction Methods 0.000 description 5
- 230000000144 pharmacologic effect Effects 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- 239000001257 hydrogen Substances 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- YJTKZCDBKVTVBY-UHFFFAOYSA-N 1,3-Diphenylbenzene Chemical group C1=CC=CC=C1C1=CC=CC(C=2C=CC=CC=2)=C1 YJTKZCDBKVTVBY-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- ZHNUHDYFZUAESO-UHFFFAOYSA-N Formamide Chemical compound NC=O ZHNUHDYFZUAESO-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 241000699670 Mus sp. Species 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 230000000202 analgesic effect Effects 0.000 description 2
- 230000003110 anti-inflammatory effect Effects 0.000 description 2
- 239000002585 base Substances 0.000 description 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 238000009833 condensation Methods 0.000 description 2
- 230000005494 condensation Effects 0.000 description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
- 239000003814 drug Substances 0.000 description 2
- 230000005764 inhibitory process Effects 0.000 description 2
- SUMDYPCJJOFFON-UHFFFAOYSA-N isethionic acid Chemical compound OCCS(O)(=O)=O SUMDYPCJJOFFON-UHFFFAOYSA-N 0.000 description 2
- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 230000001225 therapeutic effect Effects 0.000 description 2
- DKSZLDSPXIWGFO-BLOJGBSASA-N (4r,4ar,7s,7ar,12bs)-9-methoxy-3-methyl-2,4,4a,7,7a,13-hexahydro-1h-4,12-methanobenzofuro[3,2-e]isoquinoline-7-ol;phosphoric acid;hydrate Chemical compound O.OP(O)(O)=O.OP(O)(O)=O.C([C@H]1[C@H](N(CC[C@@]112)C)C3)=C[C@H](O)[C@@H]1OC1=C2C3=CC=C1OC.C([C@H]1[C@H](N(CC[C@@]112)C)C3)=C[C@H](O)[C@@H]1OC1=C2C3=CC=C1OC DKSZLDSPXIWGFO-BLOJGBSASA-N 0.000 description 1
- HAFWELDDNUXLCK-TYYBGVCCSA-N (e)-but-2-enedioic acid;hydrate Chemical compound O.OC(=O)\C=C\C(O)=O HAFWELDDNUXLCK-TYYBGVCCSA-N 0.000 description 1
- GUBGYTABKSRVRQ-XLOQQCSPSA-N Alpha-Lactose Chemical compound O[C@@H]1[C@@H](O)[C@@H](O)[C@@H](CO)O[C@H]1O[C@@H]1[C@@H](CO)O[C@H](O)[C@H](O)[C@H]1O GUBGYTABKSRVRQ-XLOQQCSPSA-N 0.000 description 1
- 239000005711 Benzoic acid Substances 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 description 1
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
- ZZSNKZQZMQGXPY-UHFFFAOYSA-N Ethyl cellulose Chemical compound CCOCC1OC(OC)C(OCC)C(OCC)C1OC1C(O)C(O)C(OC)C(CO)O1 ZZSNKZQZMQGXPY-UHFFFAOYSA-N 0.000 description 1
- 239000001856 Ethyl cellulose Substances 0.000 description 1
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 1
- 229920000084 Gum arabic Polymers 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Natural products OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 1
- JLTDJTHDQAWBAV-UHFFFAOYSA-N N,N-dimethylaniline Chemical compound CN(C)C1=CC=CC=C1 JLTDJTHDQAWBAV-UHFFFAOYSA-N 0.000 description 1
- XJUCJNCTEBRXRN-UHFFFAOYSA-N O.ClOCl Chemical compound O.ClOCl XJUCJNCTEBRXRN-UHFFFAOYSA-N 0.000 description 1
- 206010030113 Oedema Diseases 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- 241000978776 Senegalia senegal Species 0.000 description 1
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 1
- 239000000205 acacia gum Substances 0.000 description 1
- 235000010489 acacia gum Nutrition 0.000 description 1
- 150000008431 aliphatic amides Chemical class 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 229940035676 analgesics Drugs 0.000 description 1
- 238000010171 animal model Methods 0.000 description 1
- 239000000730 antalgic agent Substances 0.000 description 1
- 239000002260 anti-inflammatory agent Substances 0.000 description 1
- 229940121363 anti-inflammatory agent Drugs 0.000 description 1
- 235000010233 benzoic acid Nutrition 0.000 description 1
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- SXDBWCPKPHAZSM-UHFFFAOYSA-N bromic acid Chemical compound OBr(=O)=O SXDBWCPKPHAZSM-UHFFFAOYSA-N 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 1
- 239000000679 carrageenan Substances 0.000 description 1
- 235000010418 carrageenan Nutrition 0.000 description 1
- 229920001525 carrageenan Polymers 0.000 description 1
- 229940113118 carrageenan Drugs 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
- 235000015165 citric acid Nutrition 0.000 description 1
- 229960004415 codeine phosphate Drugs 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 229960004193 dextropropoxyphene Drugs 0.000 description 1
- XLMALTXPSGQGBX-GCJKJVERSA-N dextropropoxyphene Chemical compound C([C@](OC(=O)CC)([C@H](C)CN(C)C)C=1C=CC=CC=1)C1=CC=CC=C1 XLMALTXPSGQGBX-GCJKJVERSA-N 0.000 description 1
- 150000004683 dihydrates Chemical class 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 235000019325 ethyl cellulose Nutrition 0.000 description 1
- 229920001249 ethyl cellulose Polymers 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 235000011087 fumaric acid Nutrition 0.000 description 1
- 239000008103 glucose Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 208000027866 inflammatory disease Diseases 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 238000007912 intraperitoneal administration Methods 0.000 description 1
- 229940045996 isethionic acid Drugs 0.000 description 1
- PHTQWCKDNZKARW-UHFFFAOYSA-N isoamylol Chemical compound CC(C)CCO PHTQWCKDNZKARW-UHFFFAOYSA-N 0.000 description 1
- 239000008101 lactose Substances 0.000 description 1
- 231100000636 lethal dose Toxicity 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 231100000053 low toxicity Toxicity 0.000 description 1
- 235000019359 magnesium stearate Nutrition 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 229940098779 methanesulfonic acid Drugs 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- LNOPIUAQISRISI-UHFFFAOYSA-N n'-hydroxy-2-propan-2-ylsulfonylethanimidamide Chemical compound CC(C)S(=O)(=O)CC(N)=NO LNOPIUAQISRISI-UHFFFAOYSA-N 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- 230000008447 perception Effects 0.000 description 1
- 229960002895 phenylbutazone Drugs 0.000 description 1
- VYMDGNCVAMGZFE-UHFFFAOYSA-N phenylbutazonum Chemical compound O=C1C(CCCC)C(=O)N(C=2C=CC=CC=2)N1C1=CC=CC=C1 VYMDGNCVAMGZFE-UHFFFAOYSA-N 0.000 description 1
- 238000000053 physical method Methods 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 235000015497 potassium bicarbonate Nutrition 0.000 description 1
- 229910000028 potassium bicarbonate Inorganic materials 0.000 description 1
- 239000011736 potassium bicarbonate Substances 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 235000011181 potassium carbonates Nutrition 0.000 description 1
- TYJJADVDDVDEDZ-UHFFFAOYSA-M potassium hydrogencarbonate Chemical compound [K+].OC([O-])=O TYJJADVDDVDEDZ-UHFFFAOYSA-M 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- UIIMBOGNXHQVGW-UHFFFAOYSA-M sodium bicarbonate Substances [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 229940032330 sulfuric acid Drugs 0.000 description 1
- 208000011580 syndromic disease Diseases 0.000 description 1
- 229940066771 systemic antihistamines piperazine derivative Drugs 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 235000012222 talc Nutrition 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 238000002560 therapeutic procedure Methods 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- UHVMMEOXYDMDKI-JKYCWFKZSA-L zinc;1-(5-cyanopyridin-2-yl)-3-[(1s,2s)-2-(6-fluoro-2-hydroxy-3-propanoylphenyl)cyclopropyl]urea;diacetate Chemical compound [Zn+2].CC([O-])=O.CC([O-])=O.CCC(=O)C1=CC=C(F)C([C@H]2[C@H](C2)NC(=O)NC=2N=CC(=CC=2)C#N)=C1O UHVMMEOXYDMDKI-JKYCWFKZSA-L 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more 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, directly attached to ring carbon atoms
- C07D239/32—One oxygen, sulfur or nitrogen atom
- C07D239/42—One nitrogen atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more 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, directly attached to ring carbon atoms
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
- C07D239/48—Two nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/70—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings condensed with carbocyclic rings or ring systems
- C07D239/72—Quinazolines; Hydrogenated quinazolines
- C07D239/78—Quinazolines; Hydrogenated quinazolines with hetero atoms directly attached in position 2
- C07D239/84—Nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/70—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings condensed with carbocyclic rings or ring systems
- C07D239/72—Quinazolines; Hydrogenated quinazolines
- C07D239/86—Quinazolines; Hydrogenated quinazolines with hetero atoms directly attached in position 4
- C07D239/94—Nitrogen atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Description
Analogifremgangsmåte for fremstilling av hittil ukjente, terapeutisk aktive, disubstituerte piperazinderivater.
Nærværende oppfinnelse vedrorer en fremgangsmåte for fremstilling av hittil ukjente piperazinderivater med den generelle formel I:
: hvor
-R er et hydrogenatom eller en fenylkjerne
-Het et heterocyclisk radikal med den generelle formel II eller
: III:
<:>forbundet med piperazinresten i 2- eller ^-stilling, og hvor X •
og Y er samtidig eller alternativt
; - et hydrogenatom
; - et halogenatom : - et hydroxy-radikal - et lavere alkylradikal med inntil 5 karbonatomer i i - et lavere alkoxyradikal med inntil 5 karbonatomer - et amino-, mono-alkyl- eller alkylen-amino- eller dialkyl-amino-radikal. ! I , • j j De nye derivater ifolge oppfinnelsen har fordelaktige farmako- \ \ logiske og terapeutiske egenskaper og kan derfor brukes som I legemidler, spesielt som analgetika og betennelseshindrende j midler. i
De nye derivater kan fremstilles ved kondensasjon av et halogenert derivat med den generelle formel: ; i hvilken Het har den ovenfor angitte betydning og Z er et klor-: eller brom-atom, med et N-mono-substituert piperazin med den ; generelle formel IV:
hvor R har den ovenfor angitte betydning.
Den beste måte for å utfore fremgangsmåten består i å la det
: ovenfor beskrevne halogenerte derivat reagere med et N-mono-substituert piperazin av type IV opplost i et polart opplosnings-middel- valgt blant vanlige alkoholer med hoyt kokepunkt, slik som butanol eller isopentanol, eller horende til gruppen av N,N-disubstituerte alifatiske amider, slik som f.eks. dimethyl- '; formamid eller dimethylacetåmid. Det er fordelaktig å arbeide ved temperaturer mellom 120 og 150°C i nærvær av et hydrogensyreopptagende stoff dannet i lopet av reaksjonen. Dette hydrogensyreopptagende stoff kan enten være det i overskudd brukte valgte N-monosubstituerte piperazin eller et alkali- eller jord-alkalisalt av karbonsyren, f.eks. natrium- eller kalium-bikarbon-at eller -karbonat, kalsiumkarbonat eller en organisk tertiær base, slik som dimethylanilin, pyridin eller triethylamin.
Man kan også, hvis onsket, utfore kondensasjonen av det halo generte derivat i nærvær av et overskudd av det valgte N-monosubstituerte piperazin, som samtidig virker som opplosnings-middel og som hydrogensyreopptagende stoff, ved temperaturer mellom 120 og l50°C.
De således erholdte nye derivater, som er svake baser, kan om-dannes til addisjonssalter med syrer, og de utgjor derfor en del av oppfinnelsen. Disse addisjonssalter kan erholdes ved innvirkning av de nye derivater på syrer i passende opplbsnings-midler, som f.eks. i vann eller med vann blandbare alkoholer. Som syrer som kan brukes, for dannelsen av disse addisjonssalter kan nevnes blant de mineralske syrer: saltsyre, brom-hydrogensyre, methansulfonsyre, isethionsyre, svovelsyre, fos-for syre, sulfamidsyre, blant de organiske syrer: eddiksyre, propionsyre, maleinsyre, fumarsyre, vinsyre, sitronsyre, oxal-syre, benzoesyre osv..
Disse nye derivater kan eventuelt renses ved hjelp av fysikal-ske metoder, f.eks. ved destillasjon, krystallisasjon, kromato-grafi eller kjemiske metoder, f.eks. ved dannelse av addisjonssalter med syrer og deres dekomponering med alkaliske midler.
De nye derivater og deres addisjonssalter ifblge oppfinnelsen har fordelaktige farmakologiske og terapeutiske egenskaper og de kan derfor brukes som legemidler, spesielt som smertestillende midler og som betennelseshindrende midler.
Deres toksisitet ble undersokt hos mus på intraperitoneal vei
og på oral vei. Det er funnet at den dodelige dose for $ 0% av forsoksdyr varierer mellom 75 og 500 mg/kg av peritoneal vei og mellom 500 og 3500 mg/kg av oral vei.
For å undersoke deres smertestillende aktivitet brukes metoden med heteplaten hos mus (Woolf og Mac Donald).
Man har konstatert en okning av persepsjonsterskelen for smerter som varierer fra 25 til.>100# med doser fra 10 til 80 mg/kg intraperitonealt eller oralt. For sammenligningens skyld kan oppgis kodeinfosfat, hvis smertestillende aktivitet er ^ 0% ved •+0 mg/kg intraperitonealt, og -dimethylamino-^-methyl-3'-difenyl-1,2-butanol-2-propionat (d-propoksyfen) med 2$% ved hO mg/kg intraoralt i samme forsoket.
Man har likeledes konstatert en kraftig betennelseshindrende aktivitet som vises ved inhibering av odem i rottelabber for-årsaket av carragenin (Winter, CA og andre, Proe: Soc.Exp. Biol. 111, 5kh (1962)). Denne inhibering varierer fra 20 til ^ >50% med doser fra 10 til ^0 mg/kg oralt. For sammenligningens skyld kan det angis at -butyl-<H>-'-difenyl-1,2-pyrazolidin-dion-3,5 (fenylbutazon) har en inhiberende aktivitet på 30% ved h- 0 mg/kg oralt i det samme forsok.
De ovenfor angitte egenskaper og den svake toksisitet tillater å bruke de nye derivater for menneske- og dyreterapi, spesielt for behandling av forskjellige smertefulle syndromer og betenn-elses -sykdommer .
Derivatene kan administreres i forskjellige farmakologiske for-mer i forbindelse med farmakologiske faste eller flytende binde-midler, som f.eks. destillert vann, glukose, laktose, talkum, gummi arabicum, magnesiumstearat, ethylcellulose osv..
De anvendte doser kan variere fra 50 til 500 mg ved oral, rek-tal eller parental administrering.
De folgende eksempler viser hvordan fremgangsmåten for fremstilling av derivater ifolge oppfinnelsen skal utfores.
Smeltepunktene ble bestemt med heteplaten av Kofler under mikroskopet.
Eksempel 1
( trif enyl- 3 ' , 3 ' , 3 ' - propyl- 1') - l-( pyrimidyl- 2") - tf- piperazin.
Man går ut fra 25 g (trifenyl-3',3',3'-propyl-1')-1-piperazin (kp. n x ^ =.227 -228°C) og 8,02 g kloro-2-pyrimidin opplost
i IfOO ml dimethylformamid, i nærvær av 19,3 g tort kaliumkar-bonat, og man oppnår etter 5 timers oppvarmning ved 135°C, 22 g (trifenyl-3 ' ?3 ' ?3 ' -propyl-11) -1- (pyr imi dyl-2") -^-piperazin, som smelter ved 130°C.
Utgangs-(trifenyl-3',3'?3<1->propyl-1<1>)-1-piperazin-dimethansul-fonat smp. l8<t>f-l87°C fremstilles ved innvirkning av trifenyl-3?3,3-propanol-l-tosylat på et overskudd av vannfri piperazin ved lkO°C.
Ifolge eksempel 1 fremstilles folgende derivater:
1. (dif enyl-3 1 ,3 '-propyl-11)-1-(pyrimidyl-^-")-^-piperazin, hvis fumarat-monohydrat smelter ved 233-237°C. 2. (difenyl-3<1>,3<1-p>ropyl-1<1>)-l-(kloro-5"-pyrimidyl-2")-^-piperazin, hvis methansulfonat smelter ved 25l°C. 3 . (dif enyl-3 ' >3 1 -propyl-1') -l-(methyl-lf "-pyrimidyl-2") -^-piperazin, som smelter ved 80°C. l+. (difenyl-3',3■-pro<py>l-1<1>)-l-(dimethyl-V',5"-pyrimidyl-2")-^-piperazin, hvis fumarat smelter ved 195 - 205 under dekomponering. 5. (difenyl-3 1 ,3 ' -propyl-1 •) -1- (dimethyl-^-'» ,6"-pyrimidyl-2") - ^-piperazin, som smelter ved 103-105°C. 6. (dif enyl-3 1 ,3 ' -propyl-1') -l-(methoxy-!+"-pyrimidyl-2") - h-piperazin, som smelter ved 88°C. 7. (difenyl-3 ' ,3 1 -propyl-1') -l-(methylamino-lf"-pyrimidyl-2") -
M—piperazin, hvis diklorhydrat smelter ved 175-178°C.
8 . (difenyl-3 ' ,3 ' -propyl-1') -l-(benzopyrimidyl-2") -^--piperazin, hvis diklorhydrat smelter ved 235-2<I>fO°C. 9. (difenyl-3 1 ,3 ' -propyl-1') -l-(benzopyrimidyl-1+") -^--piperazin,
hvis diklorhydrat smelter ved 230-235°C.
10. (difenyl-31 ,3 '-propyl-1') -l-(methyl-2"-'benzopyrimidyl-1+") --piperazin, hvis fumarat-hemihydrat smelter ved 167-170 C. 11. (trifenyl-3 ' ,3 ' ,3 ' -propyl-1') -l-(hydroksy-1+"-pyrimidyl-2") - ^-piperazin, hvis diklorhydrat-hydrat smelter ved 176-l80°C
under dekomponering.
12. (trifenyl-3' ,3' ,3 '-propyl-1')-l-(methyl-lf"-pyrimidyl-2")-^-piperazin, som smelter ved 128°C.
i 13. (trifenyl-31 ,3' ,3 • -propyl-1') -l-(dimethyl-V' , 5"-pyrimidyl-2") -lf-piperazin, hvis fumarat smelter ved 190-200°C under dekomponering.
; lh. (trifenyl-3' ,3' ,3 ' -propyl-1') -l-(dimethyl-lf" ,6"-pyrimidyl-2")-^-piperazin, som smelter ved l<l>+0°C. 15. (trifenyl-3' ,3' ,3 ' -propyl-1') -l-(methoxy-lf "-pyrimidyl-2") - h-piperazin, som smelter ved 125°C. 16. (trifenyl-3 * ,3 ' ,3 ' -propyl-1') -l-(amino-1+u-pyrimidyl-2") -»f-piperazin, hvis dihydrat smelter ved 132-l<l>fO°C.
<:>17. (trifenyl-3' ,3' ,3 ' -propyl-1') -l-(amino-2"-pyrimidyl-1+") ->+-
\ piperazin, som smelter ved 188-190°C.
18. (trifenyl-3',3'>3<1->propyl-1')-l-(methylamino-<l>f"-pyrimidyl-2")-^--piperazin, som smelter ved 150-153°C.
! 19. (trifenyl-3',3',3'-propyl-1')-l-(dimethylamino-^"-pyrimidyl-i 2")-<>>+-piperazin, som smelter ved 115°C. 20. (trifenyl-3' ,3' ,3 '-propyl-1')-l-(allylamino-lf "-pyrimidyl-2")-V-piperazin, som smelter ved 151+-158 C.
21. (trifenyl-3 ' ,3 ',3 '-propyl-1')-l-(benzopyrimidyl-lf ")->+-
I piperazin, hvis diklorhydrat smelter ved 155-160°C.
22. (trifenyl-3',3',3'-propyl-1')-l-(methyl-2"-benzopyrimidyl-
• h")-^--piperazin, hvis fumarat smelter ved 205-210°C under dekomponering.
Claims (1)
- Analogi-fremgangsmåte for fremstilling av hittil ukjente tera-j peutisk aktive derivater av disubstituert piperazin med dengenerelle formel I:hvor -R er et hydrogenatom eller en fenylkjerne -Het et heterocyclisk radikal med den generelle formel II eller III:forbundet med piperazinresten i 2- eller ^--stilling, og hvor X og Y er samtidig eller alternativt: - et hydrogenatom - et halogenatom - et hydroxyradikal - et lavere alkylradikal med inntil 5 karbonatomer - et lavere alkoxyradikal med inntil 5 karbonatomer - et aminoradikal, mono-alkyl- eller alkylen-amino- eller dialkyl-amino-radikal, såvel som av deres addisjonssalter med mineralske eller organiske syrer, karakterisert ved at man kon- denserer et halogenert derivat med den generelle formeli hvilken Het har den ovenfor angitte betydning og Z er et klor-. eller bromatom, med et N-mono-substituert piperazin med den generelle formel IV:i hvilken R har den ovenfor angitte betydning. Anførte publikasjoner: Belgisk patent nr. 655.431
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB53477/65A GB1148378A (en) | 1965-12-16 | 1965-12-16 | Disubstituted piperazines and process for preparing them |
Publications (1)
Publication Number | Publication Date |
---|---|
NO121663B true NO121663B (no) | 1971-03-29 |
Family
ID=10467966
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NO166014A NO121663B (no) | 1965-12-16 | 1966-12-15 |
Country Status (13)
Country | Link |
---|---|
US (1) | US3435036A (no) |
AT (1) | AT263788B (no) |
BE (1) | BE690742A (no) |
CH (1) | CH473136A (no) |
DK (1) | DK116363B (no) |
ES (1) | ES334316A1 (no) |
FI (1) | FI45974C (no) |
FR (2) | FR1505109A (no) |
GB (1) | GB1148378A (no) |
NL (2) | NL6617743A (no) |
NO (1) | NO121663B (no) |
OA (1) | OA02181A (no) |
SE (1) | SE321682B (no) |
Families Citing this family (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1279843A (en) * | 1969-05-23 | 1972-06-28 | Science Union & Cie | Benzamidoethyl-piperazines and process for their preparation |
FR2503162A1 (fr) * | 1981-04-07 | 1982-10-08 | Pharmindustrie | Nouveaux derives de piperazino-2 pyrimidine, procedes pour leur preparation et leur utilisation comme medicaments ou comme intermediaires pour la fabrication de medicaments |
FR2527608B1 (fr) * | 1982-05-28 | 1986-10-10 | Sandoz Sa | Nouveaux composes heterocycliques, leur preparation et leur utilisation comme medicaments |
CH651027A5 (de) * | 1982-11-12 | 1985-08-30 | Sandoz Ag | Heterocyclische verbindungen, ihre herstellung und verwendung. |
US4745191A (en) * | 1987-09-30 | 1988-05-17 | American Home Products Corporation | 1-((A-substituted phenyl-ω-substituted piperazinyl)alkenyl) cyclohexanol |
IT1293804B1 (it) * | 1997-08-01 | 1999-03-10 | Recordati Chem Pharm | Diarilalchilpiperazine attive sulle basse vie urinarie |
US6399614B1 (en) | 1997-08-01 | 2002-06-04 | Recordati S.A. Chemical And Pharmaceutical Company | 1-(N-phenylaminoalkyl)piperazine derivatives substituted at position 2 of the phenyl ring |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
BE485737A (no) * | 1947-11-12 | |||
NL265777A (no) * | 1960-06-09 |
-
0
- NL NL129219D patent/NL129219C/xx active
-
1965
- 1965-12-16 GB GB53477/65A patent/GB1148378A/en not_active Expired
-
1966
- 1966-11-24 SE SE16113/66A patent/SE321682B/xx unknown
- 1966-11-24 DK DK607966AA patent/DK116363B/da unknown
- 1966-12-02 OA OA52676A patent/OA02181A/xx unknown
- 1966-12-02 FI FI663195A patent/FI45974C/fi active
- 1966-12-05 BE BE690742D patent/BE690742A/xx unknown
- 1966-12-07 US US599714A patent/US3435036A/en not_active Expired - Lifetime
- 1966-12-07 ES ES0334316A patent/ES334316A1/es not_active Expired
- 1966-12-15 FR FR87614A patent/FR1505109A/fr not_active Expired
- 1966-12-15 NO NO166014A patent/NO121663B/no unknown
- 1966-12-15 AT AT1159366A patent/AT263788B/de active
- 1966-12-16 NL NL6617743A patent/NL6617743A/xx unknown
- 1966-12-16 CH CH1803066A patent/CH473136A/fr not_active IP Right Cessation
-
1967
- 1967-03-09 FR FR98132A patent/FR6285M/fr not_active Expired
Also Published As
Publication number | Publication date |
---|---|
CH473136A (fr) | 1969-05-31 |
FR1505109A (fr) | 1967-12-08 |
DE1620419A1 (de) | 1972-03-09 |
DK116363B (da) | 1970-01-05 |
SE321682B (no) | 1970-03-16 |
NL6617743A (no) | 1967-06-19 |
BE690742A (no) | 1967-06-05 |
US3435036A (en) | 1969-03-25 |
AT263788B (de) | 1968-08-12 |
GB1148378A (en) | 1969-04-10 |
NL129219C (no) | |
FR6285M (no) | 1968-09-02 |
FI45974B (no) | 1972-07-31 |
ES334316A1 (es) | 1967-12-01 |
OA02181A (fr) | 1970-05-05 |
FI45974C (fi) | 1972-11-10 |
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