HU224312B1 - 2-Amino-indán-származékok, eljárás előállításukra és ilyen vegyületeket tartalmazó gyógyászati készítmények - Google Patents
2-Amino-indán-származékok, eljárás előállításukra és ilyen vegyületeket tartalmazó gyógyászati készítmények Download PDFInfo
- Publication number
- HU224312B1 HU224312B1 HU9800422A HUP9800422A HU224312B1 HU 224312 B1 HU224312 B1 HU 224312B1 HU 9800422 A HU9800422 A HU 9800422A HU P9800422 A HUP9800422 A HU P9800422A HU 224312 B1 HU224312 B1 HU 224312B1
- Authority
- HU
- Hungary
- Prior art keywords
- piperidine
- amino
- dihydro
- formula
- compound
- Prior art date
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- LMHHFZAXSANGGM-UHFFFAOYSA-N 2-aminoindane Chemical class C1=CC=C2CC(N)CC2=C1 LMHHFZAXSANGGM-UHFFFAOYSA-N 0.000 title claims abstract description 6
- 238000000034 method Methods 0.000 title claims description 19
- 238000002360 preparation method Methods 0.000 title claims description 9
- 239000008194 pharmaceutical composition Substances 0.000 title claims description 6
- 230000008569 process Effects 0.000 title claims description 4
- 150000001875 compounds Chemical class 0.000 claims abstract description 173
- 239000000203 mixture Substances 0.000 claims abstract description 40
- 150000003839 salts Chemical class 0.000 claims abstract description 30
- 239000001257 hydrogen Substances 0.000 claims abstract description 15
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 15
- 239000002253 acid Substances 0.000 claims abstract description 8
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 8
- 229910052736 halogen Inorganic materials 0.000 claims abstract description 7
- 150000002367 halogens Chemical class 0.000 claims abstract description 7
- 230000003287 optical effect Effects 0.000 claims abstract description 7
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 6
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical group FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims abstract description 4
- 125000003545 alkoxy group Chemical group 0.000 claims abstract description 4
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 4
- 229910052799 carbon Inorganic materials 0.000 claims abstract description 4
- 229910052731 fluorine Chemical group 0.000 claims abstract description 4
- 239000011737 fluorine Chemical group 0.000 claims abstract description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 4
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims abstract description 4
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 4
- 239000001301 oxygen Chemical group 0.000 claims abstract description 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 4
- 125000001424 substituent group Chemical group 0.000 claims abstract description 4
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims abstract description 4
- 239000003814 drug Substances 0.000 claims abstract description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract 3
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 claims description 66
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 45
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 claims description 30
- -1 chroman-8-yl Chemical group 0.000 claims description 27
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 claims description 24
- 238000011282 treatment Methods 0.000 claims description 16
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 claims description 14
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims description 11
- 239000002904 solvent Substances 0.000 claims description 11
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 claims description 10
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical group N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 8
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 8
- 208000035475 disorder Diseases 0.000 claims description 8
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 claims description 7
- AOJFQRQNPXYVLM-UHFFFAOYSA-N pyridin-1-ium;chloride Chemical compound [Cl-].C1=CC=[NH+]C=C1 AOJFQRQNPXYVLM-UHFFFAOYSA-N 0.000 claims description 6
- CDBYLPFSWZWCQE-UHFFFAOYSA-L sodium carbonate Substances [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 claims description 6
- 229910000027 potassium carbonate Inorganic materials 0.000 claims description 5
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims description 5
- 239000012279 sodium borohydride Substances 0.000 claims description 5
- 229910000033 sodium borohydride Inorganic materials 0.000 claims description 5
- 239000012321 sodium triacetoxyborohydride Substances 0.000 claims description 5
- SCYULBFZEHDVBN-UHFFFAOYSA-N 1,1-Dichloroethane Chemical compound CC(Cl)Cl SCYULBFZEHDVBN-UHFFFAOYSA-N 0.000 claims description 4
- 208000019901 Anxiety disease Diseases 0.000 claims description 4
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 4
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 4
- 239000004480 active ingredient Substances 0.000 claims description 4
- 230000036506 anxiety Effects 0.000 claims description 4
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 4
- 229910052794 bromium Inorganic materials 0.000 claims description 4
- 239000000460 chlorine Substances 0.000 claims description 4
- 229910052801 chlorine Inorganic materials 0.000 claims description 4
- 238000010438 heat treatment Methods 0.000 claims description 4
- 229910052740 iodine Inorganic materials 0.000 claims description 4
- 229910052757 nitrogen Chemical group 0.000 claims description 4
- 229910000029 sodium carbonate Inorganic materials 0.000 claims description 4
- MXNPZIASPIXENL-UHFFFAOYSA-N 1-(2,3-dihydro-1,4-benzodioxin-5-yl)-n-(6,7-dihydro-5h-cyclopenta[f][1,3]benzodioxol-6-yl)piperidin-4-amine Chemical compound O1CCOC2=C1C=CC=C2N(CC1)CCC1NC1CC(C=C2OCOC2=C2)=C2C1 MXNPZIASPIXENL-UHFFFAOYSA-N 0.000 claims description 3
- LZLFUVVRGYHCMN-UHFFFAOYSA-N 1-(3,4-dihydro-2h-chromen-8-yl)-n-(2,3-dihydro-1h-inden-2-yl)piperidin-4-amine Chemical compound C1CCOC2=C1C=CC=C2N(CC1)CCC1NC1CC2=CC=CC=C2C1 LZLFUVVRGYHCMN-UHFFFAOYSA-N 0.000 claims description 3
- FKSPATRLBQPGIQ-UHFFFAOYSA-N 2-[[1-(2,3-dihydro-1,4-benzodioxin-5-yl)piperidin-4-yl]amino]-2,3-dihydro-1h-inden-5-ol Chemical compound O1CCOC2=C1C=CC=C2N(CC1)CCC1NC1CC2=CC=C(O)C=C2C1 FKSPATRLBQPGIQ-UHFFFAOYSA-N 0.000 claims description 3
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical group [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 3
- 208000020401 Depressive disease Diseases 0.000 claims description 3
- 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 claims description 3
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 claims description 3
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 claims description 3
- 238000006268 reductive amination reaction Methods 0.000 claims description 3
- IIMOAOXQJWKTRB-UHFFFAOYSA-N 1-(1-benzofuran-7-yl)-n-(5-fluoro-2,3-dihydro-1h-inden-2-yl)piperidin-4-amine Chemical compound C1C2=CC(F)=CC=C2CC1NC(CC1)CCN1C1=CC=CC2=C1OC=C2 IIMOAOXQJWKTRB-UHFFFAOYSA-N 0.000 claims description 2
- ZHDLIVXDDCZBDR-UHFFFAOYSA-N 1-(2,3-dihydro-1,4-benzodioxin-5-yl)-n-(5,6-dimethoxy-2,3-dihydro-1h-inden-2-yl)piperidin-4-amine Chemical compound O1CCOC2=C1C=CC=C2N(CC1)CCC1NC1CC(C=C(C(=C2)OC)OC)=C2C1 ZHDLIVXDDCZBDR-UHFFFAOYSA-N 0.000 claims description 2
- RIFGFCMZLBEHKB-UHFFFAOYSA-N 1-(2,3-dihydro-1,4-benzodioxin-5-yl)-n-(5,6-dimethyl-2,3-dihydro-1h-inden-2-yl)piperidin-4-amine Chemical compound O1CCOC2=C1C=CC=C2N(CC1)CCC1NC1CC(C=C(C(=C2)C)C)=C2C1 RIFGFCMZLBEHKB-UHFFFAOYSA-N 0.000 claims description 2
- CAHPKHAYVYBJAS-UHFFFAOYSA-N 1-(2,3-dihydro-1,4-benzodioxin-5-yl)-n-(5-methoxy-2,3-dihydro-1h-inden-2-yl)piperidin-4-amine Chemical compound O1CCOC2=C1C=CC=C2N(CC1)CCC1NC1CC2=CC=C(OC)C=C2C1 CAHPKHAYVYBJAS-UHFFFAOYSA-N 0.000 claims description 2
- BUVGYTAHPWYIHL-UHFFFAOYSA-N 1-(2,3-dihydro-1,4-benzodioxin-5-yl)-n-(5-methyl-2,3-dihydro-1h-inden-2-yl)piperidin-4-amine Chemical compound O1CCOC2=C1C=CC=C2N(CC1)CCC1NC1CC2=CC=C(C)C=C2C1 BUVGYTAHPWYIHL-UHFFFAOYSA-N 0.000 claims description 2
- HPEIHRXXYHODTL-UHFFFAOYSA-N 1-(2,3-dihydro-1,4-benzodioxin-5-yl)-n-[5-(trifluoromethyl)-2,3-dihydro-1h-inden-2-yl]piperidin-4-amine Chemical compound O1CCOC2=C1C=CC=C2N(CC1)CCC1NC1CC2=CC=C(C(F)(F)F)C=C2C1 HPEIHRXXYHODTL-UHFFFAOYSA-N 0.000 claims description 2
- RJDOVNUUXOKEOU-UHFFFAOYSA-N 1-(3,4-dihydro-2h-chromen-8-yl)-n-(5-fluoro-2,3-dihydro-1h-inden-2-yl)piperidin-4-amine Chemical compound C1CCOC2=C1C=CC=C2N(CC1)CCC1NC1CC2=CC=C(F)C=C2C1 RJDOVNUUXOKEOU-UHFFFAOYSA-N 0.000 claims description 2
- GYRHSRZYIFQPEU-UHFFFAOYSA-N 1-(3,4-dihydro-2h-chromen-8-yl)-n-(5-methoxy-2,3-dihydro-1h-inden-2-yl)piperidin-4-amine Chemical compound C1CCOC2=C1C=CC=C2N(CC1)CCC1NC1CC2=CC=C(OC)C=C2C1 GYRHSRZYIFQPEU-UHFFFAOYSA-N 0.000 claims description 2
- RCBHFTIWVWXGBL-UHFFFAOYSA-N 1-(3,4-dihydro-2h-chromen-8-yl)-n-(6,7-dihydro-5h-cyclopenta[f][1,3]benzodioxol-6-yl)piperidin-4-amine Chemical compound C1CCOC2=C1C=CC=C2N(CC1)CCC1NC1CC(C=C2OCOC2=C2)=C2C1 RCBHFTIWVWXGBL-UHFFFAOYSA-N 0.000 claims description 2
- VPVYSMHKTMCEEJ-UHFFFAOYSA-N 1-(3,4-dihydro-2h-chromen-8-yl)-n-[5-(1,2,4-triazol-4-yl)-2,3-dihydro-1h-inden-2-yl]piperidin-4-amine Chemical compound C=1C=C2CC(NC3CCN(CC3)C=3C=4OCCCC=4C=CC=3)CC2=CC=1N1C=NN=C1 VPVYSMHKTMCEEJ-UHFFFAOYSA-N 0.000 claims description 2
- JNWIJVIWQUVKQS-UHFFFAOYSA-N 2-[[1-(3,4-dihydro-2h-chromen-8-yl)piperidin-4-yl]amino]-2,3-dihydro-1h-inden-5-ol Chemical compound C1CCOC2=C1C=CC=C2N(CC1)CCC1NC1CC2=CC=C(O)C=C2C1 JNWIJVIWQUVKQS-UHFFFAOYSA-N 0.000 claims description 2
- OGFMFRWOQWESLG-UHFFFAOYSA-N 8-[4-(6,7-dihydro-5h-cyclopenta[f][1,3]benzodioxol-6-ylamino)piperidin-1-yl]-3,4-dihydro-2h-chromen-4-ol Chemical compound C1C2=CC=3OCOC=3C=C2CC1NC(CC1)CCN1C1=CC=CC2=C1OCCC2O OGFMFRWOQWESLG-UHFFFAOYSA-N 0.000 claims description 2
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- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 2
- MJVBMEVMDBMTPD-UHFFFAOYSA-N n-(2,3-dihydro-1h-inden-2-yl)-1-(6-fluoro-3,4-dihydro-2h-chromen-8-yl)piperidin-4-amine Chemical compound C1C2=CC=CC=C2CC1NC(CC1)CCN1C1=CC(F)=CC2=C1OCCC2 MJVBMEVMDBMTPD-UHFFFAOYSA-N 0.000 claims description 2
- FCQFWLMWZZXDGR-UHFFFAOYSA-N n-(5-chloro-2,3-dihydro-1h-inden-2-yl)-1-(2,3-dihydro-1,4-benzodioxin-5-yl)piperidin-4-amine Chemical compound O1CCOC2=C1C=CC=C2N(CC1)CCC1NC1CC2=CC=C(Cl)C=C2C1 FCQFWLMWZZXDGR-UHFFFAOYSA-N 0.000 claims description 2
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- UNUJRVRWPYDMAF-UHFFFAOYSA-N 1-(2,3-dihydro-1,4-benzodioxin-5-yl)-n-(5-fluoro-2,3-dihydro-1h-inden-2-yl)piperidin-4-amine Chemical compound O1CCOC2=C1C=CC=C2N(CC1)CCC1NC1CC2=CC=C(F)C=C2C1 UNUJRVRWPYDMAF-UHFFFAOYSA-N 0.000 claims 2
- IKZLCMYKNSOJJR-UHFFFAOYSA-N 1-(2,3-dihydro-1,4-benzodioxin-5-yl)-n-(2,3-dihydro-1h-inden-2-yl)-4-methylpiperidin-4-amine Chemical compound C1C2=CC=CC=C2CC1NC1(C)CCN(C=2C=3OCCOC=3C=CC=2)CC1 IKZLCMYKNSOJJR-UHFFFAOYSA-N 0.000 claims 1
- PEEYUYFAZNTREO-UHFFFAOYSA-N 1-(2,3-dihydro-1,4-benzodioxin-5-yl)-n-(4,7-dimethoxy-2,3-dihydro-1h-inden-2-yl)piperidin-4-amine Chemical compound O1CCOC2=C1C=CC=C2N(CC1)CCC1NC1CC(C(OC)=CC=C2OC)=C2C1 PEEYUYFAZNTREO-UHFFFAOYSA-N 0.000 claims 1
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Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/04—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- 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
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/18—Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
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- 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
- A61P25/20—Hypnotics; Sedatives
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- 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
- A61P25/24—Antidepressants
-
- 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
- A61P25/26—Psychostimulants, e.g. nicotine, cocaine
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/04—Anorexiants; Antiobesity agents
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D411/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen and sulfur atoms as the only ring hetero atoms
- C07D411/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen and sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D411/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen and sulfur atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
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- Hematology (AREA)
- Anesthesiology (AREA)
- Child & Adolescent Psychology (AREA)
- Pain & Pain Management (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Plural Heterocyclic Compounds (AREA)
- Hydrogenated Pyridines (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR9702360A FR2760014B1 (fr) | 1997-02-27 | 1997-02-27 | Nouveaux composes de 2-amino indane, leur procede de preparation et les compositions pharmaceutiques qui les contiennent |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| HU9800422D0 HU9800422D0 (en) | 1998-04-28 |
| HUP9800422A1 HUP9800422A1 (hu) | 1999-12-28 |
| HU224312B1 true HU224312B1 (hu) | 2005-07-28 |
Family
ID=9504253
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| HU9800422A HU224312B1 (hu) | 1997-02-27 | 1998-02-26 | 2-Amino-indán-származékok, eljárás előállításukra és ilyen vegyületeket tartalmazó gyógyászati készítmények |
Country Status (18)
| Country | Link |
|---|---|
| US (1) | US5968954A (enExample) |
| EP (1) | EP0861837B1 (enExample) |
| JP (1) | JPH10237071A (enExample) |
| CN (1) | CN1090627C (enExample) |
| AT (1) | ATE265451T1 (enExample) |
| AU (1) | AU725756B2 (enExample) |
| BR (1) | BR9800763A (enExample) |
| CA (1) | CA2231025C (enExample) |
| DE (1) | DE69823411T2 (enExample) |
| DK (1) | DK0861837T3 (enExample) |
| ES (1) | ES2219853T3 (enExample) |
| FR (1) | FR2760014B1 (enExample) |
| HU (1) | HU224312B1 (enExample) |
| NO (1) | NO314307B1 (enExample) |
| NZ (1) | NZ329853A (enExample) |
| PL (1) | PL190240B1 (enExample) |
| PT (1) | PT861837E (enExample) |
| ZA (1) | ZA981680B (enExample) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TWI274750B (en) * | 1999-01-12 | 2007-03-01 | Abbott Gmbh & Co Kg | Triazole compounds showing high affinity to dopamine D3 receptor and pharmaceutical composition comprising the same |
| SE0103650D0 (sv) * | 2001-11-01 | 2001-11-01 | Astrazeneca Ab | Therapeutic heterocyclic compounds |
| KR100864356B1 (ko) * | 2001-01-16 | 2008-10-17 | 아스트라제네카 아베 | 치료용 헤테로시클릭 화합물 |
| DE60231507D1 (de) | 2001-07-20 | 2010-07-01 | Psychogenics Inc | Behandlung von hyperaktivitätsstörungen und aufmerksamkeitsdefiziten |
| JP2005343790A (ja) * | 2002-05-31 | 2005-12-15 | Ajinomoto Co Inc | カルシウムチャネル拮抗薬を含有する医薬組成物 |
| US20050165025A1 (en) * | 2004-01-22 | 2005-07-28 | Recordati Ireland Ltd. | Combination therapy with 5HT 1A and 5HT 1B-receptor antagonists |
| WO2006062063A1 (ja) * | 2004-12-08 | 2006-06-15 | Astellas Pharma Inc. | ピペリジン誘導体及びその製造法 |
| UY29892A1 (es) * | 2005-11-04 | 2007-06-29 | Astrazeneca Ab | Nuevos derivados de cromano, composiciones farmaceuticas conteniendolos, procesos de preparacion y aplicaciones |
| WO2020183011A1 (en) | 2019-03-14 | 2020-09-17 | Institut Curie | Htr1d inhibitors and uses thereof in the treatment of cancer |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB9318431D0 (en) * | 1993-09-06 | 1993-10-20 | Boots Co Plc | Therapeutic agents |
| FR2734819B1 (fr) * | 1995-05-31 | 1997-07-04 | Adir | Nouveaux composes de la piperazine, de la piperidine et de la 1,2,5,6-tetrahydropyridine, leur procede de preparation et les compositions pharmaceutiques les contenant |
-
1997
- 1997-02-27 FR FR9702360A patent/FR2760014B1/fr not_active Expired - Fee Related
-
1998
- 1998-02-24 PL PL98324982A patent/PL190240B1/pl not_active IP Right Cessation
- 1998-02-25 JP JP10042716A patent/JPH10237071A/ja active Pending
- 1998-02-25 BR BR9800763-7A patent/BR9800763A/pt not_active Application Discontinuation
- 1998-02-26 CA CA002231025A patent/CA2231025C/fr not_active Expired - Fee Related
- 1998-02-26 HU HU9800422A patent/HU224312B1/hu not_active IP Right Cessation
- 1998-02-26 NO NO19980803A patent/NO314307B1/no unknown
- 1998-02-26 US US09/031,490 patent/US5968954A/en not_active Expired - Fee Related
- 1998-02-26 CN CN98107709A patent/CN1090627C/zh not_active Expired - Fee Related
- 1998-02-26 NZ NZ329853A patent/NZ329853A/xx unknown
- 1998-02-27 DE DE69823411T patent/DE69823411T2/de not_active Expired - Fee Related
- 1998-02-27 AU AU56359/98A patent/AU725756B2/en not_active Ceased
- 1998-02-27 ES ES98400469T patent/ES2219853T3/es not_active Expired - Lifetime
- 1998-02-27 ZA ZA981680A patent/ZA981680B/xx unknown
- 1998-02-27 PT PT98400469T patent/PT861837E/pt unknown
- 1998-02-27 AT AT98400469T patent/ATE265451T1/de not_active IP Right Cessation
- 1998-02-27 EP EP98400469A patent/EP0861837B1/fr not_active Expired - Lifetime
- 1998-02-27 DK DK98400469T patent/DK0861837T3/da active
Also Published As
| Publication number | Publication date |
|---|---|
| CN1194983A (zh) | 1998-10-07 |
| DE69823411T2 (de) | 2005-02-17 |
| NZ329853A (en) | 1999-01-28 |
| JPH10237071A (ja) | 1998-09-08 |
| DE69823411D1 (de) | 2004-06-03 |
| AU725756B2 (en) | 2000-10-19 |
| EP0861837B1 (fr) | 2004-04-28 |
| FR2760014B1 (fr) | 1999-04-09 |
| PT861837E (pt) | 2004-07-30 |
| ES2219853T3 (es) | 2004-12-01 |
| HK1014945A1 (en) | 1999-10-08 |
| HUP9800422A1 (hu) | 1999-12-28 |
| PL324982A1 (en) | 1998-08-31 |
| CA2231025C (fr) | 2003-09-16 |
| HU9800422D0 (en) | 1998-04-28 |
| ZA981680B (en) | 1998-09-04 |
| AU5635998A (en) | 1998-09-03 |
| NO980803L (no) | 1998-08-28 |
| DK0861837T3 (da) | 2004-08-16 |
| BR9800763A (pt) | 1999-12-07 |
| CA2231025A1 (fr) | 1998-08-27 |
| PL190240B1 (pl) | 2005-11-30 |
| FR2760014A1 (fr) | 1998-08-28 |
| EP0861837A1 (fr) | 1998-09-02 |
| CN1090627C (zh) | 2002-09-11 |
| ATE265451T1 (de) | 2004-05-15 |
| NO314307B1 (no) | 2003-03-03 |
| US5968954A (en) | 1999-10-19 |
| NO980803D0 (no) | 1998-02-26 |
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| Date | Code | Title | Description |
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| HFG4 | Patent granted, date of granting |
Effective date: 20050613 |
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| MM4A | Lapse of definitive patent protection due to non-payment of fees |