FI107916B - Menetelmä hydratsonijohdannaisten valmistamiseksi - Google Patents
Menetelmä hydratsonijohdannaisten valmistamiseksi Download PDFInfo
- Publication number
- FI107916B FI107916B FI912164A FI912164A FI107916B FI 107916 B FI107916 B FI 107916B FI 912164 A FI912164 A FI 912164A FI 912164 A FI912164 A FI 912164A FI 107916 B FI107916 B FI 107916B
- Authority
- FI
- Finland
- Prior art keywords
- formula
- indanone
- mmol
- compound
- amidino
- Prior art date
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- 238000000034 method Methods 0.000 title claims description 27
- 238000002360 preparation method Methods 0.000 title claims description 15
- 230000008569 process Effects 0.000 title claims description 14
- 150000007857 hydrazones Chemical class 0.000 title claims description 9
- 150000001875 compounds Chemical class 0.000 claims abstract description 89
- 150000003839 salts Chemical class 0.000 claims abstract description 31
- 239000001257 hydrogen Substances 0.000 claims abstract description 17
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 17
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 10
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 9
- 150000002431 hydrogen Chemical group 0.000 claims abstract description 7
- 239000007858 starting material Substances 0.000 claims description 33
- -1 thiocarbamoyl Chemical group 0.000 claims description 29
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 12
- 150000001412 amines Chemical class 0.000 claims description 4
- 125000003545 alkoxy group Chemical group 0.000 claims description 2
- ATDGTVJJHBUTRL-UHFFFAOYSA-N cyanogen bromide Chemical compound BrC#N ATDGTVJJHBUTRL-UHFFFAOYSA-N 0.000 claims description 2
- 125000004356 hydroxy functional group Chemical group O* 0.000 claims 1
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 claims 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract description 4
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract description 3
- 206010028980 Neoplasm Diseases 0.000 abstract description 2
- 125000001424 substituent group Chemical group 0.000 abstract description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 39
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 37
- 239000000243 solution Substances 0.000 description 29
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 27
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 27
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 21
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 21
- 239000000203 mixture Substances 0.000 description 20
- 239000011541 reaction mixture Substances 0.000 description 18
- 239000004480 active ingredient Substances 0.000 description 17
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 16
- 238000006243 chemical reaction Methods 0.000 description 15
- 239000013078 crystal Substances 0.000 description 15
- 238000005160 1H NMR spectroscopy Methods 0.000 description 14
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 14
- 125000004093 cyano group Chemical group *C#N 0.000 description 14
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 12
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 12
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 11
- 238000004992 fast atom bombardment mass spectroscopy Methods 0.000 description 11
- 238000001816 cooling Methods 0.000 description 10
- 102000005758 Adenosylmethionine decarboxylase Human genes 0.000 description 9
- 108010070753 Adenosylmethionine decarboxylase Proteins 0.000 description 9
- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Substances [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 9
- OTXHZHQQWQTQMW-UHFFFAOYSA-N (diaminomethylideneamino)azanium;hydrogen carbonate Chemical compound OC([O-])=O.N[NH2+]C(N)=N OTXHZHQQWQTQMW-UHFFFAOYSA-N 0.000 description 7
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 7
- 239000002253 acid Substances 0.000 description 7
- 235000019270 ammonium chloride Nutrition 0.000 description 7
- 229910000037 hydrogen sulfide Inorganic materials 0.000 description 7
- 238000003756 stirring Methods 0.000 description 7
- AZUYLZMQTIKGSC-UHFFFAOYSA-N 1-[6-[4-(5-chloro-6-methyl-1H-indazol-4-yl)-5-methyl-3-(1-methylindazol-5-yl)pyrazol-1-yl]-2-azaspiro[3.3]heptan-2-yl]prop-2-en-1-one Chemical compound ClC=1C(=C2C=NNC2=CC=1C)C=1C(=NN(C=1C)C1CC2(CN(C2)C(C=C)=O)C1)C=1C=C2C=NN(C2=CC=1)C AZUYLZMQTIKGSC-UHFFFAOYSA-N 0.000 description 6
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 6
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 6
- 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 6
- 238000005481 NMR spectroscopy Methods 0.000 description 6
- 229920002472 Starch Polymers 0.000 description 6
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 6
- 239000002775 capsule Substances 0.000 description 6
- DOBRDRYODQBAMW-UHFFFAOYSA-N copper(i) cyanide Chemical compound [Cu+].N#[C-] DOBRDRYODQBAMW-UHFFFAOYSA-N 0.000 description 6
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 6
- 239000008187 granular material Substances 0.000 description 5
- QNXSIUBBGPHDDE-UHFFFAOYSA-N indan-1-one Chemical compound C1=CC=C2C(=O)CCC2=C1 QNXSIUBBGPHDDE-UHFFFAOYSA-N 0.000 description 5
- 235000019359 magnesium stearate Nutrition 0.000 description 5
- 239000012074 organic phase Substances 0.000 description 5
- 229920000768 polyamine Polymers 0.000 description 5
- 229920001223 polyethylene glycol Polymers 0.000 description 5
- 239000002243 precursor Substances 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- 235000019698 starch Nutrition 0.000 description 5
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 235000019439 ethyl acetate Nutrition 0.000 description 4
- 239000000546 pharmaceutical excipient Substances 0.000 description 4
- 239000000825 pharmaceutical preparation Substances 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 239000000454 talc Substances 0.000 description 4
- 229910052623 talc Inorganic materials 0.000 description 4
- 235000012222 talc Nutrition 0.000 description 4
- MWFDDDJSDSYEHN-UHFFFAOYSA-N 1-oxo-2,3-dihydroindene-4-carboximidamide;hydrochloride Chemical compound Cl.NC(=N)C1=CC=CC2=C1CCC2=O MWFDDDJSDSYEHN-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 3
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 3
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 3
- 102000004190 Enzymes Human genes 0.000 description 3
- 108090000790 Enzymes Proteins 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 3
- 239000002202 Polyethylene glycol Substances 0.000 description 3
- 150000001409 amidines Chemical group 0.000 description 3
- HAMNKKUPIHEESI-UHFFFAOYSA-N aminoguanidine Chemical class NNC(N)=N HAMNKKUPIHEESI-UHFFFAOYSA-N 0.000 description 3
- 229910021529 ammonia Inorganic materials 0.000 description 3
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 3
- 229910052794 bromium Inorganic materials 0.000 description 3
- 239000003112 inhibitor Substances 0.000 description 3
- 230000005764 inhibitory process Effects 0.000 description 3
- 238000007911 parenteral administration Methods 0.000 description 3
- 239000008194 pharmaceutical composition Substances 0.000 description 3
- 238000010992 reflux Methods 0.000 description 3
- 239000000600 sorbitol Substances 0.000 description 3
- 239000008107 starch Substances 0.000 description 3
- SCTBWJINDJVNDM-UHFFFAOYSA-N 1-oxo-2,3-dihydroindene-4-carbonitrile Chemical compound C1=CC=C(C#N)C2=C1C(=O)CC2 SCTBWJINDJVNDM-UHFFFAOYSA-N 0.000 description 2
- CBMDOHQMIOJGKT-UHFFFAOYSA-N 2-methyl-1-oxo-2,3-dihydroindene-4-carbonitrile Chemical compound O=C1C(C)CC2=C1C=CC=C2C#N CBMDOHQMIOJGKT-UHFFFAOYSA-N 0.000 description 2
- OSPYFQJVCPXMIL-UHFFFAOYSA-N 2-methyl-1-oxo-2,3-dihydroindene-4-carboximidamide;hydrochloride Chemical compound Cl.O=C1C(C)CC2=C1C=CC=C2C(N)=N OSPYFQJVCPXMIL-UHFFFAOYSA-N 0.000 description 2
- HMIWFYCTSXDOLD-UHFFFAOYSA-N 3-methyl-1-oxo-2,3-dihydroindene-4-carboximidamide;hydrochloride Chemical compound Cl.C1=CC(C(N)=N)=C2C(C)CC(=O)C2=C1 HMIWFYCTSXDOLD-UHFFFAOYSA-N 0.000 description 2
- KLBVVAYZHZJLFR-UHFFFAOYSA-N 4-bromo-6,7-dimethyl-2,3-dihydroinden-1-one Chemical compound CC1=CC(Br)=C2CCC(=O)C2=C1C KLBVVAYZHZJLFR-UHFFFAOYSA-N 0.000 description 2
- VIHLGHRPFVEQBU-UHFFFAOYSA-N 5-oxo-7,8-dihydro-6h-naphthalene-1-carbonitrile Chemical compound C1=CC=C2C(=O)CCCC2=C1C#N VIHLGHRPFVEQBU-UHFFFAOYSA-N 0.000 description 2
- PUTKZZMENBTIMV-UHFFFAOYSA-N 5-oxo-7,8-dihydro-6h-naphthalene-1-carbothioamide Chemical compound O=C1CCCC2=C1C=CC=C2C(=S)N PUTKZZMENBTIMV-UHFFFAOYSA-N 0.000 description 2
- WEKHLJQDSUVDMQ-UHFFFAOYSA-N 5-oxo-7,8-dihydro-6h-naphthalene-1-carboximidamide;hydrochloride Chemical compound Cl.O=C1CCCC2=C1C=CC=C2C(=N)N WEKHLJQDSUVDMQ-UHFFFAOYSA-N 0.000 description 2
- ULQBAJGPKCJDGT-UHFFFAOYSA-N 6,7-dimethoxy-1-oxo-2,3-dihydroindene-4-carboximidamide;hydrochloride Chemical compound Cl.COC1=CC(C(N)=N)=C2CCC(=O)C2=C1OC ULQBAJGPKCJDGT-UHFFFAOYSA-N 0.000 description 2
- YVGLRQPPHKUROE-UHFFFAOYSA-N 6,7-dimethyl-1-oxo-2,3-dihydroindene-4-carboximidamide;hydrochloride Chemical compound Cl.CC1=CC(C(N)=N)=C2CCC(=O)C2=C1C YVGLRQPPHKUROE-UHFFFAOYSA-N 0.000 description 2
- 102000016893 Amine Oxidase (Copper-Containing) Human genes 0.000 description 2
- 108010028700 Amine Oxidase (Copper-Containing) Proteins 0.000 description 2
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- 229920002261 Corn starch Polymers 0.000 description 2
- IAZDPXIOMUYVGZ-WFGJKAKNSA-N Dimethyl sulfoxide Chemical compound [2H]C([2H])([2H])S(=O)C([2H])([2H])[2H] IAZDPXIOMUYVGZ-WFGJKAKNSA-N 0.000 description 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- WTDHULULXKLSOZ-UHFFFAOYSA-N Hydroxylamine hydrochloride Chemical compound Cl.ON WTDHULULXKLSOZ-UHFFFAOYSA-N 0.000 description 2
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- 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
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- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
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- QDRKDTQENPPHOJ-UHFFFAOYSA-N sodium ethoxide Chemical compound [Na+].CC[O-] QDRKDTQENPPHOJ-UHFFFAOYSA-N 0.000 description 1
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- 239000004408 titanium dioxide Substances 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
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- 235000019731 tricalcium phosphate Nutrition 0.000 description 1
- 229940078499 tricalcium phosphate Drugs 0.000 description 1
- 229910000391 tricalcium phosphate Inorganic materials 0.000 description 1
- DWCSXQCXXITVKE-UHFFFAOYSA-N triethyloxidanium Chemical compound CC[O+](CC)CC DWCSXQCXXITVKE-UHFFFAOYSA-N 0.000 description 1
- 201000002311 trypanosomiasis Diseases 0.000 description 1
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- 229910052720 vanadium Inorganic materials 0.000 description 1
- 229940100445 wheat starch Drugs 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C337/00—Derivatives of thiocarbonic acids containing functional groups covered by groups C07C333/00 or C07C335/00 in which at least one nitrogen atom of these functional groups is further bound to another nitrogen atom not being part of a nitro or nitroso group
- C07C337/06—Compounds containing any of the groups, e.g. thiosemicarbazides
- C07C337/08—Compounds containing any of the groups, e.g. thiosemicarbazides the other nitrogen atom being further doubly-bound to a carbon atom, e.g. thiosemicarbazones
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
- A61P33/02—Antiprotozoals, e.g. for leishmaniasis, trichomoniasis, toxoplasmosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
- A61P33/02—Antiprotozoals, e.g. for leishmaniasis, trichomoniasis, toxoplasmosis
- A61P33/06—Antimalarials
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- 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
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C243/00—Compounds containing chains of nitrogen atoms singly-bound to each other, e.g. hydrazines, triazanes
- C07C243/10—Hydrazines
- C07C243/20—Hydrazines having nitrogen atoms of hydrazine groups bound to carbon atoms of rings other than six-membered aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C281/00—Derivatives of carbonic acid containing functional groups covered by groups C07C269/00 - C07C279/00 in which at least one nitrogen atom of these functional groups is further bound to another nitrogen atom not being part of a nitro or nitroso group
- C07C281/06—Compounds containing any of the groups, e.g. semicarbazides
- C07C281/08—Compounds containing any of the groups, e.g. semicarbazides the other nitrogen atom being further doubly-bound to a carbon atom, e.g. semicarbazones
- C07C281/12—Compounds containing any of the groups, e.g. semicarbazides the other nitrogen atom being further doubly-bound to a carbon atom, e.g. semicarbazones the carbon atom being part of a ring other than a six-membered aromatic ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C281/00—Derivatives of carbonic acid containing functional groups covered by groups C07C269/00 - C07C279/00 in which at least one nitrogen atom of these functional groups is further bound to another nitrogen atom not being part of a nitro or nitroso group
- C07C281/16—Compounds containing any of the groups, e.g. aminoguanidine
- C07C281/18—Compounds containing any of the groups, e.g. aminoguanidine the other nitrogen atom being further doubly-bound to a carbon atom, e.g. guanylhydrazones
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2602/00—Systems containing two condensed rings
- C07C2602/02—Systems containing two condensed rings the rings having only two atoms in common
- C07C2602/04—One of the condensed rings being a six-membered aromatic ring
- C07C2602/06—One of the condensed rings being a six-membered aromatic ring the other ring being four-membered
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2602/00—Systems containing two condensed rings
- C07C2602/02—Systems containing two condensed rings the rings having only two atoms in common
- C07C2602/04—One of the condensed rings being a six-membered aromatic ring
- C07C2602/08—One of the condensed rings being a six-membered aromatic ring the other ring being five-membered, e.g. indane
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- General Health & Medical Sciences (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)
- Tropical Medicine & Parasitology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Materials For Photolithography (AREA)
- Plural Heterocyclic Compounds (AREA)
- Peptides Or Proteins (AREA)
- Wire Bonding (AREA)
- Diaphragms For Electromechanical Transducers (AREA)
- Ultra Sonic Daignosis Equipment (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH153890 | 1990-05-07 | ||
| CH153890 | 1990-05-07 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| FI912164A0 FI912164A0 (fi) | 1991-05-03 |
| FI912164L FI912164L (fi) | 1991-11-08 |
| FI107916B true FI107916B (fi) | 2001-10-31 |
Family
ID=4212764
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| FI912164A FI107916B (fi) | 1990-05-07 | 1991-05-03 | Menetelmä hydratsonijohdannaisten valmistamiseksi |
Country Status (26)
| Country | Link |
|---|---|
| EP (1) | EP0456133B1 (cs) |
| JP (1) | JP2565602B2 (cs) |
| KR (1) | KR100203234B1 (cs) |
| AT (1) | ATE119878T1 (cs) |
| AU (1) | AU645799B2 (cs) |
| CA (1) | CA2041832C (cs) |
| CY (1) | CY2080B1 (cs) |
| CZ (1) | CZ279340B6 (cs) |
| DE (1) | DE59104930D1 (cs) |
| DK (1) | DK0456133T3 (cs) |
| ES (1) | ES2069768T3 (cs) |
| FI (1) | FI107916B (cs) |
| GR (1) | GR3015574T3 (cs) |
| HK (1) | HK1000919A1 (cs) |
| HU (1) | HU218221B (cs) |
| ID (1) | ID1040B (cs) |
| IE (1) | IE66157B1 (cs) |
| IL (1) | IL98008A (cs) |
| NO (1) | NO175097C (cs) |
| NZ (1) | NZ238033A (cs) |
| PT (1) | PT97571B (cs) |
| RU (2) | RU2057748C1 (cs) |
| SA (1) | SA91120283B1 (cs) |
| SK (1) | SK279136B6 (cs) |
| TW (1) | TW202428B (cs) |
| ZA (1) | ZA913391B (cs) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5395855A (en) * | 1990-05-07 | 1995-03-07 | Ciba-Geigy Corporation | Hydrazones |
| RU2081108C1 (ru) * | 1991-10-16 | 1997-06-10 | Циба-Гейги АГ | Аддитивные соли кислот с основанием и фармацевтическая композиция, обладающая противоопухолевой активностью |
| EP0566446B1 (fr) * | 1992-04-03 | 1996-02-07 | Innothera | Dérivés d'indane-1, 3-dione et d'indane-1,2,3-trione, leurs procédés de préparation et leur application en thérapeutique |
| ES2103166B1 (es) * | 1992-08-26 | 1998-04-01 | Ciba Geigy Ag | Procedimiento para la obtencion de amidinohidrazonas biciclicas. |
| FR2710639B1 (fr) * | 1993-10-01 | 1995-12-22 | Innothera Lab Sa | Dérivés d'indane cétoniques, leur procédé d'obtention, leur application thérapeutique. |
| EP0808309B1 (en) * | 1995-01-26 | 2004-10-06 | Novartis AG | Imidazole derivatives, their preparation and their use as s-adenosylmethionine decarboxylase (=samdc) inhibitors |
| EP1408028A1 (en) * | 2002-10-09 | 2004-04-14 | Institut National De La Sante Et De La Recherche Medicale (Inserm) | S-adenosyl methionine decarboxylase inhibition for the treatment of a herpes simplex virus infection |
| EP1834669A1 (en) * | 2006-03-15 | 2007-09-19 | Heinrich-Pette-Institut | Use of specific hydrazone compounds for the treatment of viral infections |
| EP1884515A1 (en) * | 2006-07-31 | 2008-02-06 | Laboratorios del Dr. Esteve S.A. | Substituted indanyl sulfonamide compounds, their preparation and use as medicaments |
| CN102627593A (zh) * | 2012-02-23 | 2012-08-08 | 河南师范大学 | 具有抗癌活性的1，4-二羟基-2-甲酰基-9，10蒽醌缩氨硫脲新化合物及制备方法 |
| JP6621815B2 (ja) * | 2014-07-02 | 2019-12-18 | インフレクティス・バイオサイエンス | Ｏ−アルキル−ベンジリデングアニジン誘導体、及びミスフォールドタンパク質の蓄積と関連する障害の処置のための治療的使用 |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL7407469A (nl) * | 1974-06-01 | 1975-12-03 | Akzo Nv | Nieuwe amidinohydrazonverbindingen. |
| DE3416695A1 (de) * | 1984-05-05 | 1985-11-07 | Bayer Ag, 5090 Leverkusen | Amidinohydrazone von tetralin-, chromon-, thiochromon- und tretrahydrochinolin-derivaten, verfahren zu ihrer herstellung sowie ihre verwendung in arzneimitteln |
| WO1990007495A1 (en) * | 1988-12-27 | 1990-07-12 | E.I. Du Pont De Nemours And Company | Substituted semicarbazone arthropodicides |
-
1991
- 1991-04-26 AU AU75967/91A patent/AU645799B2/en not_active Ceased
- 1991-04-30 IL IL9800891A patent/IL98008A/en not_active IP Right Cessation
- 1991-05-02 TW TW080103460A patent/TW202428B/zh not_active IP Right Cessation
- 1991-05-03 NZ NZ238033A patent/NZ238033A/xx unknown
- 1991-05-03 CA CA002041832A patent/CA2041832C/en not_active Expired - Lifetime
- 1991-05-03 AT AT91107225T patent/ATE119878T1/de not_active IP Right Cessation
- 1991-05-03 DE DE59104930T patent/DE59104930D1/de not_active Expired - Fee Related
- 1991-05-03 ES ES91107225T patent/ES2069768T3/es not_active Expired - Lifetime
- 1991-05-03 FI FI912164A patent/FI107916B/fi active
- 1991-05-03 EP EP91107225A patent/EP0456133B1/de not_active Expired - Lifetime
- 1991-05-03 DK DK91107225.4T patent/DK0456133T3/da not_active Application Discontinuation
- 1991-05-06 RU SU914895338A patent/RU2057748C1/ru active
- 1991-05-06 HU HU519/91A patent/HU218221B/hu not_active IP Right Cessation
- 1991-05-06 ZA ZA913391A patent/ZA913391B/xx unknown
- 1991-05-06 SK SK1317-91A patent/SK279136B6/sk not_active IP Right Cessation
- 1991-05-06 NO NO911777A patent/NO175097C/no not_active IP Right Cessation
- 1991-05-06 CZ CS911317A patent/CZ279340B6/cs not_active IP Right Cessation
- 1991-05-06 KR KR1019910007285A patent/KR100203234B1/ko not_active Expired - Fee Related
- 1991-05-06 PT PT97571A patent/PT97571B/pt not_active IP Right Cessation
- 1991-05-06 IE IE153091A patent/IE66157B1/en not_active IP Right Cessation
- 1991-05-07 JP JP3101512A patent/JP2565602B2/ja not_active Expired - Fee Related
- 1991-12-17 SA SA91120283A patent/SA91120283B1/ar unknown
-
1992
- 1992-01-30 ID IDP189692A patent/ID1040B/id unknown
- 1992-10-23 RU RU9292004359A patent/RU2066311C1/ru active
-
1995
- 1995-03-30 GR GR950400746T patent/GR3015574T3/el unknown
-
1997
- 1997-11-06 HK HK97102109A patent/HK1000919A1/xx not_active IP Right Cessation
-
1998
- 1998-10-16 CY CY9802080A patent/CY2080B1/xx unknown
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| GB | Transfer or assigment of application |
Owner name: NOVARTIS AG |