SI9520096A - Derivati 2,7-substituiranega oktahidro-1H-pirido /1,2-a/ pirazina - Google Patents
Derivati 2,7-substituiranega oktahidro-1H-pirido /1,2-a/ pirazina Download PDFInfo
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- SI9520096A SI9520096A SI9520096A SI9520096A SI9520096A SI 9520096 A SI9520096 A SI 9520096A SI 9520096 A SI9520096 A SI 9520096A SI 9520096 A SI9520096 A SI 9520096A SI 9520096 A SI9520096 A SI 9520096A
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- SI
- Slovenia
- Prior art keywords
- pyrido
- octahydro
- pyrazine
- methyl
- mmol
- Prior art date
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- KYQCOXFCLRTKLS-UHFFFAOYSA-N Pyrazine Chemical class C1=CN=CC=N1 KYQCOXFCLRTKLS-UHFFFAOYSA-N 0.000 title claims description 25
- VYFYYTLLBUKUHU-UHFFFAOYSA-N dopamine Chemical compound NCCC1=CC=C(O)C(O)=C1 VYFYYTLLBUKUHU-UHFFFAOYSA-N 0.000 claims abstract description 80
- 229960003638 dopamine Drugs 0.000 claims abstract description 40
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims abstract description 16
- 108050004812 Dopamine receptor Proteins 0.000 claims abstract description 12
- 102000015554 Dopamine receptor Human genes 0.000 claims abstract description 12
- 239000003446 ligand Substances 0.000 claims abstract description 9
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 9
- 229910052717 sulfur Inorganic materials 0.000 claims abstract description 7
- 239000002243 precursor Substances 0.000 claims abstract description 4
- PJEAHOHAPYWSEB-UHFFFAOYSA-N 4h-pyrido[1,2-a]pyrazine Chemical class C1=CC=CN2CC=NC=C21 PJEAHOHAPYWSEB-UHFFFAOYSA-N 0.000 claims abstract 2
- 125000006615 aromatic heterocyclic group Chemical group 0.000 claims abstract 2
- 125000002837 carbocyclic group Chemical group 0.000 claims abstract 2
- 150000001875 compounds Chemical class 0.000 claims description 193
- -1 benzoxazolonyl Chemical group 0.000 claims description 166
- 150000003839 salts Chemical class 0.000 claims description 52
- 102000005962 receptors Human genes 0.000 claims description 22
- 108020003175 receptors Proteins 0.000 claims description 22
- 230000002265 prevention Effects 0.000 claims description 21
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 19
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 17
- 239000000460 chlorine Substances 0.000 claims description 14
- 230000005062 synaptic transmission Effects 0.000 claims description 13
- QDKWLJJOYIFEBS-UHFFFAOYSA-N 1-fluoro-4-$l^{1}-oxidanylbenzene Chemical group [O]C1=CC=C(F)C=C1 QDKWLJJOYIFEBS-UHFFFAOYSA-N 0.000 claims description 12
- 241000124008 Mammalia Species 0.000 claims description 12
- PCNDJXKNXGMECE-UHFFFAOYSA-N Phenazine Natural products C1=CC=CC2=NC3=CC=CC=C3N=C21 PCNDJXKNXGMECE-UHFFFAOYSA-N 0.000 claims description 12
- 125000001041 indolyl group Chemical group 0.000 claims description 10
- 201000010099 disease Diseases 0.000 claims description 9
- 125000001207 fluorophenyl group Chemical group 0.000 claims description 9
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 8
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 8
- 229910052739 hydrogen Inorganic materials 0.000 claims description 8
- 125000001424 substituent group Chemical group 0.000 claims description 8
- 125000003545 alkoxy group Chemical group 0.000 claims description 7
- 239000001257 hydrogen Substances 0.000 claims description 7
- 239000008194 pharmaceutical composition Substances 0.000 claims description 7
- 125000001255 4-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1F 0.000 claims description 6
- 230000004075 alteration Effects 0.000 claims description 6
- 125000003785 benzimidazolyl group Chemical group N1=C(NC2=C1C=CC=C2)* 0.000 claims description 6
- 125000004802 cyanophenyl group Chemical group 0.000 claims description 6
- 125000004212 difluorophenyl group Chemical group 0.000 claims description 6
- 229910052736 halogen Inorganic materials 0.000 claims description 6
- 150000002367 halogens Chemical class 0.000 claims description 6
- 125000001624 naphthyl group Chemical group 0.000 claims description 6
- 125000005493 quinolyl group Chemical group 0.000 claims description 6
- 239000011737 fluorine Substances 0.000 claims description 5
- 229910052731 fluorine Inorganic materials 0.000 claims description 5
- 125000001153 fluoro group Chemical group F* 0.000 claims description 5
- 230000003287 optical effect Effects 0.000 claims description 5
- 125000003373 pyrazinyl group Chemical group 0.000 claims description 5
- XRKCPDJKDFJNRF-JQWIXIFHSA-N [(7s,9as)-2-(5-fluoropyrimidin-2-yl)-1,3,4,6,7,8,9,9a-octahydropyrido[1,2-a]pyrazin-7-yl]methanol Chemical compound C([C@@H]1CC[C@@H](CN1CC1)CO)N1C1=NC=C(F)C=N1 XRKCPDJKDFJNRF-JQWIXIFHSA-N 0.000 claims description 4
- 230000008859 change Effects 0.000 claims description 4
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 4
- 230000003291 dopaminomimetic effect Effects 0.000 claims description 4
- 125000002098 pyridazinyl group Chemical group 0.000 claims description 4
- 125000004076 pyridyl group Chemical group 0.000 claims description 4
- 125000000714 pyrimidinyl group Chemical group 0.000 claims description 4
- QXWNESOGWFJDFR-YOEHRIQHSA-N (7s,9as)-7-[(4-fluorophenoxy)methyl]-2-(5-fluoropyrimidin-2-yl)-1,3,4,6,7,8,9,9a-octahydropyrido[1,2-a]pyrazine Chemical compound C1=CC(F)=CC=C1OC[C@@H]1CN2CCN(C=3N=CC(F)=CN=3)C[C@@H]2CC1 QXWNESOGWFJDFR-YOEHRIQHSA-N 0.000 claims description 3
- XRKCPDJKDFJNRF-PWSUYJOCSA-N [(7r,9as)-2-(5-fluoropyrimidin-2-yl)-1,3,4,6,7,8,9,9a-octahydropyrido[1,2-a]pyrazin-7-yl]methanol Chemical compound C([C@@H]1CC[C@H](CN1CC1)CO)N1C1=NC=C(F)C=N1 XRKCPDJKDFJNRF-PWSUYJOCSA-N 0.000 claims description 3
- MHMFGULWPTUZHT-AAEUAGOBSA-N [(7s,9as)-2-(5-chloropyridin-2-yl)-1,3,4,6,7,8,9,9a-octahydropyrido[1,2-a]pyrazin-7-yl]methanol Chemical compound C([C@@H]1CC[C@@H](CN1CC1)CO)N1C1=CC=C(Cl)C=N1 MHMFGULWPTUZHT-AAEUAGOBSA-N 0.000 claims description 3
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 3
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 3
- 229910052794 bromium Inorganic materials 0.000 claims description 3
- 229910052801 chlorine Inorganic materials 0.000 claims description 3
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 3
- MKVHLRXFOTVBAA-XGENFCTJSA-N (7R,9aS)-2-(5-chloropyridin-2-yl)-7-(3,5-difluorophenoxy)-1-methyl-1,3,4,6,7,8,9,9a-octahydropyrido[1,2-a]pyrazine Chemical compound FC=1C=C(O[C@@H]2CC[C@@H]3N(CCN(C3C)C3=NC=C(C=C3)Cl)C2)C=C(C=1)F MKVHLRXFOTVBAA-XGENFCTJSA-N 0.000 claims description 2
- CPHPZMUBAIAMOO-YMSDKTMASA-N (7R,9aS)-2-(5-fluoropyrimidin-2-yl)-7-(4-iodophenoxy)-1-methyl-1,3,4,6,7,8,9,9a-octahydropyrido[1,2-a]pyrazine Chemical compound IC1=CC=C(O[C@@H]2CC[C@@H]3N(CCN(C3C)C3=NC=C(C=N3)F)C2)C=C1 CPHPZMUBAIAMOO-YMSDKTMASA-N 0.000 claims description 2
- IXDSLGRVOZUEHM-CGDWMNPFSA-N (7R,9aS)-7-(4-fluorophenoxy)-2-(4-fluorophenyl)-1-methyl-1,3,4,6,7,8,9,9a-octahydropyrido[1,2-a]pyrazine Chemical compound FC1=CC=C(O[C@@H]2CC[C@@H]3N(CCN(C3C)C3=CC=C(C=C3)F)C2)C=C1 IXDSLGRVOZUEHM-CGDWMNPFSA-N 0.000 claims description 2
- MWQXNDNIVONUPG-RHGDZWTLSA-N (7S,9aS)-2-(5-fluoropyrimidin-2-yl)-1-methyl-7-[3-(trifluoromethoxy)phenoxy]-1,3,4,6,7,8,9,9a-octahydropyrido[1,2-a]pyrazine Chemical compound FC(OC=1C=C(O[C@H]2CC[C@@H]3N(CCN(C3C)C3=NC=C(C=N3)F)C2)C=CC=1)(F)F MWQXNDNIVONUPG-RHGDZWTLSA-N 0.000 claims description 2
- DDLMXDXJVCLTCF-QAPCUYQASA-N (7r,9as)-2-(5-chloropyridin-2-yl)-7-[(4-fluorophenoxy)methyl]-1,3,4,6,7,8,9,9a-octahydropyrido[1,2-a]pyrazine Chemical compound C1=CC(F)=CC=C1OC[C@H]1CN2CCN(C=3N=CC(Cl)=CC=3)C[C@@H]2CC1 DDLMXDXJVCLTCF-QAPCUYQASA-N 0.000 claims description 2
- HYBNCSFXHTVEQG-SQJZIBIZSA-N (7s,9as)-2-(5-chloropyridin-2-yl)-7-(4-fluorophenoxy)-1-methyl-1,3,4,6,7,8,9,9a-octahydropyrido[1,2-a]pyrazine Chemical compound C([C@H](CC[C@H]1C2C)OC=3C=CC(F)=CC=3)N1CCN2C1=CC=C(Cl)C=N1 HYBNCSFXHTVEQG-SQJZIBIZSA-N 0.000 claims description 2
- NMEQZMPJYPCFIQ-BRQZFJGMSA-N 3-[[(7R,9aS)-2-(5-fluoropyrimidin-2-yl)-1-methyl-1,3,4,6,7,8,9,9a-octahydropyrido[1,2-a]pyrazin-7-yl]oxy]benzonitrile Chemical compound C(#N)C=1C=C(O[C@@H]2CC[C@@H]3N(CCN(C3C)C3=NC=C(C=N3)F)C2)C=CC=1 NMEQZMPJYPCFIQ-BRQZFJGMSA-N 0.000 claims description 2
- LJDKJDRKMZQOTL-BRQZFJGMSA-N 4-[[(7R,9aS)-2-(5-fluoropyrimidin-2-yl)-1-methyl-1,3,4,6,7,8,9,9a-octahydropyrido[1,2-a]pyrazin-7-yl]oxy]benzonitrile Chemical compound C(#N)C1=CC=C(O[C@@H]2CC[C@@H]3N(CCN(C3C)C3=NC=C(C=N3)F)C2)C=C1 LJDKJDRKMZQOTL-BRQZFJGMSA-N 0.000 claims description 2
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 2
- FAOGGEZCOWGBNP-GQHGFMKCSA-N FC1=CC(=C(O[C@H]2CC[C@@H]3N(CCN(C3C)C3=NC=C(C=N3)F)C2)C=C1)C(F)(F)F Chemical compound FC1=CC(=C(O[C@H]2CC[C@@H]3N(CCN(C3C)C3=NC=C(C=N3)F)C2)C=C1)C(F)(F)F FAOGGEZCOWGBNP-GQHGFMKCSA-N 0.000 claims description 2
- JNTKJIKMABSIHS-YMSDKTMASA-N FC1=CC=C(O[C@@H]2CC[C@@H]3N(CCN(C3C)C3=NC=C(C=N3)F)C2)C=C1 Chemical compound FC1=CC=C(O[C@@H]2CC[C@@H]3N(CCN(C3C)C3=NC=C(C=N3)F)C2)C=C1 JNTKJIKMABSIHS-YMSDKTMASA-N 0.000 claims description 2
- MKVHLRXFOTVBAA-LNXOFFIKSA-N FC=1C=C(O[C@H]2CC[C@@H]3N(CCN(C3C)C3=NC=C(C=C3)Cl)C2)C=C(C=1)F Chemical compound FC=1C=C(O[C@H]2CC[C@@H]3N(CCN(C3C)C3=NC=C(C=C3)Cl)C2)C=C(C=1)F MKVHLRXFOTVBAA-LNXOFFIKSA-N 0.000 claims description 2
- 125000004618 benzofuryl group Chemical group O1C(=CC2=C1C=CC=C2)* 0.000 claims description 2
- 125000004196 benzothienyl group Chemical group S1C(=CC2=C1C=CC=C2)* 0.000 claims description 2
- 125000004541 benzoxazolyl group Chemical group O1C(=NC2=C1C=CC=C2)* 0.000 claims description 2
- 125000002541 furyl group Chemical group 0.000 claims description 2
- 150000002431 hydrogen Chemical class 0.000 claims description 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 2
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 2
- 125000002971 oxazolyl group Chemical group 0.000 claims description 2
- 125000001544 thienyl group Chemical group 0.000 claims description 2
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 claims description 2
- DSGQBBRNPFRMTC-IROOXBOJSA-N (7S,9aS)-2-(5-fluoropyrimidin-2-yl)-1-methyl-7-(3-methylphenoxy)-1,3,4,6,7,8,9,9a-octahydropyrido[1,2-a]pyrazine Chemical compound CC=1C=C(O[C@H]2CC[C@@H]3N(CCN(C3C)C3=NC=C(C=N3)F)C2)C=CC=1 DSGQBBRNPFRMTC-IROOXBOJSA-N 0.000 claims 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims 1
- MHMFGULWPTUZHT-YPMHNXCESA-N [(7r,9as)-2-(5-chloropyridin-2-yl)-1,3,4,6,7,8,9,9a-octahydropyrido[1,2-a]pyrazin-7-yl]methanol Chemical compound C([C@@H]1CC[C@H](CN1CC1)CO)N1C1=CC=C(Cl)C=N1 MHMFGULWPTUZHT-YPMHNXCESA-N 0.000 claims 1
- 208000035475 disorder Diseases 0.000 abstract description 6
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 226
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 132
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 102
- 239000000203 mixture Substances 0.000 description 100
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 96
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 86
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 86
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 84
- 239000000243 solution Substances 0.000 description 84
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 73
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 68
- 238000002360 preparation method Methods 0.000 description 57
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 55
- 238000000034 method Methods 0.000 description 55
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 54
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 53
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 48
- 235000019341 magnesium sulphate Nutrition 0.000 description 48
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 43
- 238000003818 flash chromatography Methods 0.000 description 43
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 38
- 238000000746 purification Methods 0.000 description 37
- 239000000741 silica gel Substances 0.000 description 37
- 229910002027 silica gel Inorganic materials 0.000 description 37
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 34
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 34
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 34
- 239000010410 layer Substances 0.000 description 32
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 30
- 238000006243 chemical reaction Methods 0.000 description 30
- 239000012074 organic phase Substances 0.000 description 29
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 28
- RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical compound C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 0.000 description 25
- 239000002904 solvent Substances 0.000 description 24
- 239000002585 base Substances 0.000 description 23
- 125000000246 pyrimidin-2-yl group Chemical group [H]C1=NC(*)=NC([H])=C1[H] 0.000 description 21
- GXWNSJYVSIJRLS-UHFFFAOYSA-N 6-bromo-8-methylimidazo[1,2-a]pyrazine Chemical class CC1=NC(Br)=CN2C=CN=C12 GXWNSJYVSIJRLS-UHFFFAOYSA-N 0.000 description 19
- 239000012442 inert solvent Substances 0.000 description 17
- 239000002253 acid Substances 0.000 description 16
- 239000012044 organic layer Substances 0.000 description 16
- 239000007787 solid Substances 0.000 description 16
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 15
- 239000000908 ammonium hydroxide Substances 0.000 description 15
- 239000008346 aqueous phase Substances 0.000 description 15
- 229910000029 sodium carbonate Inorganic materials 0.000 description 15
- FAMRKDQNMBBFBR-BQYQJAHWSA-N diethyl azodicarboxylate Substances CCOC(=O)\N=N\C(=O)OCC FAMRKDQNMBBFBR-BQYQJAHWSA-N 0.000 description 14
- FAMRKDQNMBBFBR-UHFFFAOYSA-N ethyl n-ethoxycarbonyliminocarbamate Chemical compound CCOC(=O)N=NC(=O)OCC FAMRKDQNMBBFBR-UHFFFAOYSA-N 0.000 description 14
- 239000000126 substance Substances 0.000 description 14
- IUKDDYAECHPPRM-UHFFFAOYSA-N 2,3,4,6,7,8,9,9a-octahydro-1h-pyrido[1,2-a]pyrazin-7-ylmethanol Chemical compound C1NCCN2CC(CO)CCC21 IUKDDYAECHPPRM-UHFFFAOYSA-N 0.000 description 13
- AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 description 13
- RHMPLDJJXGPMEX-UHFFFAOYSA-N 4-fluorophenol Chemical compound OC1=CC=C(F)C=C1 RHMPLDJJXGPMEX-UHFFFAOYSA-N 0.000 description 12
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 12
- 239000000047 product Substances 0.000 description 12
- 229910052938 sodium sulfate Inorganic materials 0.000 description 12
- 235000011152 sodium sulphate Nutrition 0.000 description 12
- MZRVEZGGRBJDDB-UHFFFAOYSA-N N-Butyllithium Chemical compound [Li]CCCC MZRVEZGGRBJDDB-UHFFFAOYSA-N 0.000 description 10
- DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 10
- 125000000217 alkyl group Chemical group 0.000 description 10
- 229940086542 triethylamine Drugs 0.000 description 10
- 238000003745 diagnosis Methods 0.000 description 9
- 238000002844 melting Methods 0.000 description 9
- 230000008018 melting Effects 0.000 description 9
- 239000012359 Methanesulfonyl chloride Substances 0.000 description 8
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 8
- 150000001299 aldehydes Chemical class 0.000 description 8
- 239000012267 brine Substances 0.000 description 8
- 239000000543 intermediate Substances 0.000 description 8
- PHTQWCKDNZKARW-UHFFFAOYSA-N isoamylol Chemical compound CC(C)CCO PHTQWCKDNZKARW-UHFFFAOYSA-N 0.000 description 8
- QARBMVPHQWIHKH-UHFFFAOYSA-N methanesulfonyl chloride Chemical compound CS(Cl)(=O)=O QARBMVPHQWIHKH-UHFFFAOYSA-N 0.000 description 8
- CTSLXHKWHWQRSH-UHFFFAOYSA-N oxalyl chloride Chemical compound ClC(=O)C(Cl)=O CTSLXHKWHWQRSH-UHFFFAOYSA-N 0.000 description 8
- 230000008569 process Effects 0.000 description 8
- 239000011541 reaction mixture Substances 0.000 description 8
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 8
- 230000015572 biosynthetic process Effects 0.000 description 7
- 230000000694 effects Effects 0.000 description 7
- 239000004533 oil dispersion Substances 0.000 description 7
- 229910000104 sodium hydride Inorganic materials 0.000 description 7
- UKFJLHLYPJBMCY-NEPJUHHUSA-N tert-butyl (7r,9as)-7-(hydroxymethyl)-1,3,4,6,7,8,9,9a-octahydropyrido[1,2-a]pyrazine-2-carboxylate Chemical compound C1[C@H](CO)CC[C@H]2CN(C(=O)OC(C)(C)C)CCN21 UKFJLHLYPJBMCY-NEPJUHHUSA-N 0.000 description 7
- UNCQVRBWJWWJBF-UHFFFAOYSA-N 2-chloropyrimidine Chemical compound ClC1=NC=CC=N1 UNCQVRBWJWWJBF-UHFFFAOYSA-N 0.000 description 6
- XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 description 6
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 6
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 238000004458 analytical method Methods 0.000 description 6
- 230000027455 binding Effects 0.000 description 6
- 239000003054 catalyst Substances 0.000 description 6
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Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- 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
- C07D471/02—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 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- A—HUMAN NECESSITIES
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- Health & Medical Sciences (AREA)
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- Organic Chemistry (AREA)
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- Bioinformatics & Cheminformatics (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Psychiatry (AREA)
- Hospice & Palliative Care (AREA)
- Ophthalmology & Optometry (AREA)
- Anesthesiology (AREA)
- Addiction (AREA)
- Psychology (AREA)
- Otolaryngology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US31547094A | 1994-09-30 | 1994-09-30 | |
| PCT/IB1995/000689 WO1996010571A1 (en) | 1994-09-30 | 1995-08-24 | 2,7-SUBSTITUTED OCTAHYDRO-1H-PYRIDO[1,2-a]PYRAZINE DERIVATIVES |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SI9520096A true SI9520096A (sl) | 1998-04-30 |
Family
ID=23224581
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SI9520096A SI9520096A (sl) | 1994-09-30 | 1995-08-24 | Derivati 2,7-substituiranega oktahidro-1H-pirido /1,2-a/ pirazina |
Country Status (34)
| Country | Link |
|---|---|
| US (1) | US5852031A (cs) |
| EP (1) | EP0783503B1 (cs) |
| JP (1) | JP3287574B2 (cs) |
| KR (1) | KR100244848B1 (cs) |
| CN (1) | CN1068327C (cs) |
| AT (1) | ATE209648T1 (cs) |
| AU (1) | AU681310B2 (cs) |
| BR (1) | BR9504230A (cs) |
| CA (1) | CA2200959C (cs) |
| CO (1) | CO4410335A1 (cs) |
| CZ (1) | CZ285090B6 (cs) |
| DE (1) | DE69524241T2 (cs) |
| DK (1) | DK0783503T3 (cs) |
| ES (1) | ES2166830T3 (cs) |
| FI (1) | FI113655B (cs) |
| HR (1) | HRP950507B1 (cs) |
| HU (1) | HUT77354A (cs) |
| IL (1) | IL115384A (cs) |
| MX (1) | MX9702350A (cs) |
| MY (1) | MY113729A (cs) |
| NO (1) | NO308995B1 (cs) |
| NZ (1) | NZ290936A (cs) |
| PE (1) | PE47196A1 (cs) |
| PL (1) | PL180899B1 (cs) |
| PT (1) | PT783503E (cs) |
| RU (1) | RU2163239C2 (cs) |
| SI (1) | SI9520096A (cs) |
| SK (1) | SK284341B6 (cs) |
| TR (1) | TR199501194A2 (cs) |
| TW (1) | TW406081B (cs) |
| UA (1) | UA50720C2 (cs) |
| WO (1) | WO1996010571A1 (cs) |
| YU (1) | YU63795A (cs) |
| ZA (1) | ZA958223B (cs) |
Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6231833B1 (en) * | 1999-08-05 | 2001-05-15 | Pfizer Inc | 2,7-substituted octahydro-1H-pyrido[1,2-A]pyrazine derivatives as ligands for serotonin receptors |
| US6992188B1 (en) | 1995-12-08 | 2006-01-31 | Pfizer, Inc. | Substituted heterocyclic derivatives |
| CA2240594C (en) * | 1995-12-21 | 2001-07-24 | Pfizer Limited | 2,7-substituted octahydro-pyrrolo¬1,2-a|pyrazine derivatives |
| US6281216B1 (en) * | 1998-02-09 | 2001-08-28 | Duphar International Research B.V. | 2-aminoquinoline derivatives having d4-agonistic activity |
| EP0953567A3 (en) | 1998-04-29 | 2003-04-02 | Pfizer Products Inc. | Bicyclic substituted piperazine-, piperidine- and tetrahydropyridine derivatives, their preparation and their use as agents with central dopaminergic (dopamine D4 receptor) activity |
| GT199900060A (es) * | 1998-05-22 | 2000-10-14 | Polimorfos de un monoclorhidrato de pirazina cristalino y sus composiciones farmacèuticas. | |
| GB0010757D0 (en) | 2000-05-05 | 2000-06-28 | Astrazeneca Ab | Chemical compounds |
| GB0011013D0 (en) * | 2000-05-09 | 2000-06-28 | Astrazeneca Ab | Chemical compounds |
| EP1177792A3 (en) | 2000-07-27 | 2002-10-23 | Pfizer Products Inc. | Dopamine D4 Ligands for the treatment of novelty-seeking disorders |
| US6670476B2 (en) | 2000-11-29 | 2003-12-30 | Pfizer Inc. | Resolution of trans-7-(hydroxy-methyl)octa-hydro-2H-pyrido[1,2-a]pyrazine |
| GB0121941D0 (en) | 2001-09-11 | 2001-10-31 | Astrazeneca Ab | Chemical compounds |
| EP1479676A1 (en) * | 2003-05-19 | 2004-11-24 | Aventis Pharma Deutschland GmbH | Benzimidazole-derivatives as factor xa inhibitors |
| SA04250304B1 (ar) * | 2003-09-26 | 2009-03-11 | سولفاي فارماسوتيكالز بي . في | مشتقات هكسا - واوكتاهيدرو - بيريدو {1،2-a} بيرازين ذات نشاط مضاد لـ nk1 |
Family Cites Families (22)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3388128A (en) * | 1965-09-03 | 1968-06-11 | Allan R. Day | Substituted 1, 4-diazabicyclo [4. 4. 9] decanes |
| US4182763A (en) * | 1978-05-22 | 1980-01-08 | Mead Johnson & Company | Buspirone anti-anxiety method |
| US4517187A (en) * | 1982-10-18 | 1985-05-14 | Pennwalt Corporation | 1,3,4,6,7-11b-Hexahydro-7-phenyl-2H-pyrazino[2,1-a]isoquinolines methods of preparation, and use as antidepressants |
| EP0173634B1 (fr) * | 1984-08-07 | 1988-08-31 | Cortial S.A. | Nouveaux dérivés d'(arylpipérazinyléthylaminoéthoxy)-4 phénol, leur méthode de préparation et leur application thérapeutique |
| US4704390A (en) * | 1986-02-13 | 1987-11-03 | Warner-Lambert Company | Phenyl and heterocyclic tetrahydropyridyl alkoxy-benzheterocyclic compounds as antipsychotic agents |
| IT1204803B (it) * | 1986-02-17 | 1989-03-10 | Acraf | Composto farmacologicamente attivo e composizioni farmaceutiche che lo contengono,procedimento per prepararlo e intermedio utile in detto procedimento |
| US4788290A (en) * | 1987-12-11 | 1988-11-29 | American Home Products Corporation | Serotonergic pyrazine derivatives |
| SE8803429D0 (sv) * | 1988-09-28 | 1988-09-28 | Pharmacia Ab | Novel pyridyl- and pyrimidyl derivatives |
| MX19222A (es) * | 1989-01-23 | 1993-12-01 | Pfizer | Agentes ansioliticos bis-aza-biciclicos |
| ATE120746T1 (de) * | 1991-01-31 | 1995-04-15 | Pfizer | Recematspaltung von trans-2-(2-pyrimidinyl)-7- (hydroxymethyl)octahydro-2h-pyrido(1,2-a>- pyrazin. |
| CA2195622C (en) * | 1991-02-27 | 1999-08-17 | Frank J. Urban | Process for preparing trans-piperidine-2,5-dicarboxylates |
| US5185449A (en) * | 1991-02-27 | 1993-02-09 | Pfizer Inc. | Process and intermediate for certain bis-aza-bicyclic anxiolytic agents |
| US5157034A (en) * | 1991-02-27 | 1992-10-20 | Pfizer Inc. | Neuroleptic perhydro-1H-pyrido[1,2-a]pyrazines |
| BR9206541A (pt) * | 1991-09-25 | 1995-04-25 | Pfizer | Per-hidro-1h-pirido(1,2-a)pirazinas 2-substituídas neurolépticas |
| EP0646116B1 (en) * | 1992-06-16 | 1999-10-13 | Pfizer Inc. | Process and intermediates for bis-aza-bicyclic anxiolytic agents |
| CA2146019A1 (en) * | 1992-10-23 | 1994-05-11 | Howard B. Broughton | Dopamine receptor subtype ligands |
| EP0665840A1 (en) * | 1992-10-23 | 1995-08-09 | MERCK SHARP & DOHME LTD. | Dopamine receptor subtype ligands |
| FI954088A0 (fi) * | 1993-03-01 | 1995-08-31 | Merck Sharp & Dohme | Pyrrolopyridiinijohdannaisia |
| WO1994020459A2 (en) * | 1993-03-01 | 1994-09-15 | Merck Sharp & Dohme Limited | Pyrrolo-pyridine derivatives as dopamine receptor ligands |
| US5576319A (en) * | 1993-03-01 | 1996-11-19 | Merck, Sharp & Dohme Ltd. | Pyrrolo-pyridine derivatives |
| WO1994020471A1 (en) * | 1993-03-05 | 1994-09-15 | Merck Sharp & Dohme Limited | Quinolone derivatives as dopamine d4 ligands |
| GB9416162D0 (en) * | 1994-08-10 | 1994-09-28 | Merck Sharp & Dohme | Therapeutic agents |
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1995
- 1995-08-24 CA CA002200959A patent/CA2200959C/en not_active Expired - Fee Related
- 1995-08-24 AT AT95927915T patent/ATE209648T1/de not_active IP Right Cessation
- 1995-08-24 JP JP51155196A patent/JP3287574B2/ja not_active Expired - Lifetime
- 1995-08-24 SK SK325-97A patent/SK284341B6/sk unknown
- 1995-08-24 CZ CZ97947A patent/CZ285090B6/cs not_active IP Right Cessation
- 1995-08-24 DK DK95927915T patent/DK0783503T3/da active
- 1995-08-24 EP EP95927915A patent/EP0783503B1/en not_active Expired - Lifetime
- 1995-08-24 MX MX9702350A patent/MX9702350A/es unknown
- 1995-08-24 PT PT95927915T patent/PT783503E/pt unknown
- 1995-08-24 DE DE69524241T patent/DE69524241T2/de not_active Expired - Lifetime
- 1995-08-24 KR KR1019970702080A patent/KR100244848B1/ko not_active Expired - Fee Related
- 1995-08-24 PL PL95319636A patent/PL180899B1/pl not_active IP Right Cessation
- 1995-08-24 ES ES95927915T patent/ES2166830T3/es not_active Expired - Lifetime
- 1995-08-24 US US08/809,145 patent/US5852031A/en not_active Expired - Lifetime
- 1995-08-24 NZ NZ290936A patent/NZ290936A/en unknown
- 1995-08-24 WO PCT/IB1995/000689 patent/WO1996010571A1/en active IP Right Grant
- 1995-08-24 RU RU97105362/04A patent/RU2163239C2/ru not_active IP Right Cessation
- 1995-08-24 CN CN95195356A patent/CN1068327C/zh not_active Expired - Fee Related
- 1995-08-24 AU AU31893/95A patent/AU681310B2/en not_active Ceased
- 1995-08-24 SI SI9520096A patent/SI9520096A/sl not_active IP Right Cessation
- 1995-08-24 UA UA97031431A patent/UA50720C2/uk unknown
- 1995-08-24 HU HU9702037A patent/HUT77354A/hu unknown
- 1995-09-18 TW TW084109759A patent/TW406081B/zh not_active IP Right Cessation
- 1995-09-21 IL IL11538495A patent/IL115384A/xx active IP Right Grant
- 1995-09-25 MY MYPI95002850A patent/MY113729A/en unknown
- 1995-09-26 PE PE1995279990A patent/PE47196A1/es not_active Application Discontinuation
- 1995-09-28 CO CO95045095A patent/CO4410335A1/es unknown
- 1995-09-29 YU YU63795A patent/YU63795A/sh unknown
- 1995-09-29 TR TR95/01194A patent/TR199501194A2/xx unknown
- 1995-09-29 ZA ZA958223A patent/ZA958223B/xx unknown
- 1995-09-29 BR BR9504230A patent/BR9504230A/pt not_active IP Right Cessation
- 1995-09-29 HR HR950507A patent/HRP950507B1/xx not_active IP Right Cessation
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1997
- 1997-03-25 NO NO971416A patent/NO308995B1/no unknown
- 1997-03-27 FI FI971310A patent/FI113655B/fi not_active IP Right Cessation
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