NO743980L - - Google Patents
Info
- Publication number
- NO743980L NO743980L NO743980A NO743980A NO743980L NO 743980 L NO743980 L NO 743980L NO 743980 A NO743980 A NO 743980A NO 743980 A NO743980 A NO 743980A NO 743980 L NO743980 L NO 743980L
- Authority
- NO
- Norway
- Prior art keywords
- general formula
- methyl
- substituted
- compound
- residue
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 claims description 42
- 150000008366 benzophenones Chemical class 0.000 claims description 16
- 238000000034 method Methods 0.000 claims description 14
- 229910052801 chlorine Inorganic materials 0.000 claims description 12
- -1 unsaturated alkyl radical Chemical class 0.000 claims description 11
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 10
- 150000001412 amines Chemical class 0.000 claims description 10
- 229910052736 halogen Inorganic materials 0.000 claims description 10
- 150000003839 salts Chemical class 0.000 claims description 10
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical group [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 9
- 239000002253 acid Substances 0.000 claims description 9
- 125000004432 carbon atom Chemical group C* 0.000 claims description 9
- 239000000460 chlorine Chemical group 0.000 claims description 9
- 150000002367 halogens Chemical class 0.000 claims description 9
- 239000001257 hydrogen Substances 0.000 claims description 8
- 229910052739 hydrogen Inorganic materials 0.000 claims description 8
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical compound BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 7
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 7
- 229910052794 bromium Inorganic materials 0.000 claims description 4
- 238000004519 manufacturing process Methods 0.000 claims description 4
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical compound [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 claims description 3
- 125000001931 aliphatic group Chemical group 0.000 claims description 3
- 150000005840 aryl radicals Chemical class 0.000 claims description 3
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 3
- 238000003776 cleavage reaction Methods 0.000 claims description 3
- 229910052731 fluorine Inorganic materials 0.000 claims description 3
- 239000011737 fluorine Substances 0.000 claims description 3
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 3
- 229920006395 saturated elastomer Polymers 0.000 claims description 3
- 230000007017 scission Effects 0.000 claims description 3
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 3
- 125000001153 fluoro group Chemical group F* 0.000 claims description 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 2
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- 150000002431 hydrogen Chemical class 0.000 claims 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 30
- 238000006243 chemical reaction Methods 0.000 description 26
- 239000002904 solvent Substances 0.000 description 19
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 18
- 238000002844 melting Methods 0.000 description 16
- 230000008018 melting Effects 0.000 description 16
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 12
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 12
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 12
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 11
- 238000010992 reflux Methods 0.000 description 10
- 150000002576 ketones Chemical class 0.000 description 9
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Substances [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 9
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 8
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 8
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 8
- 238000001816 cooling Methods 0.000 description 8
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 8
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 7
- 239000000203 mixture Substances 0.000 description 7
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 6
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 6
- 150000005826 halohydrocarbons Chemical class 0.000 description 6
- 239000003208 petroleum Substances 0.000 description 6
- 238000003756 stirring Methods 0.000 description 6
- 239000008096 xylene Substances 0.000 description 6
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 5
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 5
- 150000002170 ethers Chemical class 0.000 description 5
- 239000012442 inert solvent Substances 0.000 description 5
- 229910000027 potassium carbonate Inorganic materials 0.000 description 5
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 4
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 4
- 239000012948 isocyanate Substances 0.000 description 4
- 150000002513 isocyanates Chemical class 0.000 description 4
- 239000008164 mustard oil Substances 0.000 description 4
- 230000000144 pharmacologic effect Effects 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-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
- 239000002585 base Substances 0.000 description 3
- 238000009835 boiling Methods 0.000 description 3
- 150000001768 cations Chemical class 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 229910052740 iodine Inorganic materials 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- JHSJXTNCWSQPAX-UHFFFAOYSA-N n-(2-benzoyl-4-chlorophenyl)-2-(methylamino)acetamide Chemical compound CNCC(=O)NC1=CC=C(Cl)C=C1C(=O)C1=CC=CC=C1 JHSJXTNCWSQPAX-UHFFFAOYSA-N 0.000 description 3
- 230000035484 reaction time Effects 0.000 description 3
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 3
- KWTSXDURSIMDCE-UHFFFAOYSA-N 1-phenylpropan-2-amine Chemical compound CC(N)CC1=CC=CC=C1 KWTSXDURSIMDCE-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- JLTDJTHDQAWBAV-UHFFFAOYSA-N N,N-dimethylaniline Chemical compound CN(C)C1=CC=CC=C1 JLTDJTHDQAWBAV-UHFFFAOYSA-N 0.000 description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- ZOJBYZNEUISWFT-UHFFFAOYSA-N allyl isothiocyanate Chemical compound C=CCN=C=S ZOJBYZNEUISWFT-UHFFFAOYSA-N 0.000 description 2
- 150000001408 amides Chemical class 0.000 description 2
- 229910021529 ammonia Inorganic materials 0.000 description 2
- 239000011230 binding agent Substances 0.000 description 2
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 2
- 230000009194 climbing Effects 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 239000003814 drug Substances 0.000 description 2
- 229940079593 drug Drugs 0.000 description 2
- 239000003937 drug carrier Substances 0.000 description 2
- LELOWRISYMNNSU-UHFFFAOYSA-N hydrogen cyanide Chemical compound N#C LELOWRISYMNNSU-UHFFFAOYSA-N 0.000 description 2
- 238000011835 investigation Methods 0.000 description 2
- HCDBNZCIIIRKNY-UHFFFAOYSA-N n-(2-benzoyl-4-chlorophenyl)-2-[methyl(phenylcarbamoyl)amino]acetamide Chemical compound C=1C=CC=CC=1NC(=O)N(C)CC(=O)NC1=CC=C(Cl)C=C1C(=O)C1=CC=CC=C1 HCDBNZCIIIRKNY-UHFFFAOYSA-N 0.000 description 2
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
- 239000012074 organic phase Substances 0.000 description 2
- 239000000825 pharmaceutical preparation Substances 0.000 description 2
- DGTNSSLYPYDJGL-UHFFFAOYSA-N phenyl isocyanate Chemical compound O=C=NC1=CC=CC=C1 DGTNSSLYPYDJGL-UHFFFAOYSA-N 0.000 description 2
- QKFJKGMPGYROCL-UHFFFAOYSA-N phenyl isothiocyanate Chemical compound S=C=NC1=CC=CC=C1 QKFJKGMPGYROCL-UHFFFAOYSA-N 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- MAOBFOXLCJIFLV-UHFFFAOYSA-N (2-aminophenyl)-phenylmethanone Chemical compound NC1=CC=CC=C1C(=O)C1=CC=CC=C1 MAOBFOXLCJIFLV-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- BHPQYMZQTOCNFJ-UHFFFAOYSA-N Calcium cation Chemical compound [Ca+2] BHPQYMZQTOCNFJ-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- XFXPMWWXUTWYJX-UHFFFAOYSA-N Cyanide Chemical compound N#[C-] XFXPMWWXUTWYJX-UHFFFAOYSA-N 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
- AEMRFAOFKBGASW-UHFFFAOYSA-N Glycolic acid Chemical class OCC(O)=O AEMRFAOFKBGASW-UHFFFAOYSA-N 0.000 description 1
- CPELXLSAUQHCOX-UHFFFAOYSA-N Hydrogen bromide Chemical class Br CPELXLSAUQHCOX-UHFFFAOYSA-N 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
- 241001465754 Metazoa Species 0.000 description 1
- 241000699670 Mus sp. 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
- ROGCCHDNDFRFFI-UHFFFAOYSA-N N-(2-benzoyl-4-chlorophenyl)-2-[methyl(propan-2-ylcarbamoyl)amino]acetamide Chemical compound CC(C)NC(=O)N(C)CC(=O)NC1=CC=C(Cl)C=C1C(=O)C1=CC=CC=C1 ROGCCHDNDFRFFI-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 150000001242 acetic acid derivatives Chemical class 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 230000016571 aggressive behavior Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- QKSKPIVNLNLAAV-UHFFFAOYSA-N bis(2-chloroethyl) sulfide Chemical group ClCCSCCCl QKSKPIVNLNLAAV-UHFFFAOYSA-N 0.000 description 1
- IARQGJRRIUEUIB-UHFFFAOYSA-N butyl 3-[[2-(2-benzoyl-4-chloroanilino)-2-oxoethyl]-methylamino]propanoate;hydrochloride Chemical compound Cl.CCCCOC(=O)CCN(C)CC(=O)NC1=CC=C(Cl)C=C1C(=O)C1=CC=CC=C1 IARQGJRRIUEUIB-UHFFFAOYSA-N 0.000 description 1
- 229910001424 calcium ion Inorganic materials 0.000 description 1
- 239000002775 capsule Substances 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 210000003169 central nervous system Anatomy 0.000 description 1
- 239000003874 central nervous system depressant Substances 0.000 description 1
- 150000001860 citric acid derivatives Chemical class 0.000 description 1
- 230000000994 depressogenic effect Effects 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- WUFRLWZWPOKBPK-UHFFFAOYSA-N ethyl n-[2-(2-benzoyl-4-chloro-n-methylanilino)-2-oxoethyl]carbamate;hydrochloride Chemical compound Cl.CCOC(=O)NCC(=O)N(C)C1=CC=C(Cl)C=C1C(=O)C1=CC=CC=C1 WUFRLWZWPOKBPK-UHFFFAOYSA-N 0.000 description 1
- 239000000284 extract Substances 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 125000002485 formyl group Chemical class [H]C(*)=O 0.000 description 1
- VZCYOOQTPOCHFL-OWOJBTEDSA-L fumarate(2-) Chemical class [O-]C(=O)\C=C\C([O-])=O VZCYOOQTPOCHFL-OWOJBTEDSA-L 0.000 description 1
- 150000008282 halocarbons Chemical class 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 150000003840 hydrochlorides Chemical class 0.000 description 1
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 1
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 150000003893 lactate salts Chemical class 0.000 description 1
- 150000002688 maleic acid derivatives Chemical class 0.000 description 1
- 150000004701 malic acid derivatives Chemical class 0.000 description 1
- 125000001160 methoxycarbonyl group Chemical group [H]C([H])([H])OC(*)=O 0.000 description 1
- IIFWVDFOSGRJDU-UHFFFAOYSA-N n-(2-benzoyl-4-chlorophenyl)-2-[ethylcarbamoyl(methyl)amino]acetamide Chemical compound CCNC(=O)N(C)CC(=O)NC1=CC=C(Cl)C=C1C(=O)C1=CC=CC=C1 IIFWVDFOSGRJDU-UHFFFAOYSA-N 0.000 description 1
- ZXECILZJADMSAV-UHFFFAOYSA-N n-(2-benzoyl-4-chlorophenyl)-2-[methyl(phenylcarbamothioyl)amino]acetamide Chemical compound C=1C=CC=CC=1NC(=S)N(C)CC(=O)NC1=CC=C(Cl)C=C1C(=O)C1=CC=CC=C1 ZXECILZJADMSAV-UHFFFAOYSA-N 0.000 description 1
- GZEXVQJHSUDDLU-UHFFFAOYSA-N n-[4-chloro-2-(2-chlorobenzoyl)phenyl]-2-(phenylcarbamothioylamino)acetamide Chemical compound C=1C=CC=C(Cl)C=1C(=O)C1=CC(Cl)=CC=C1NC(=O)CNC(=S)NC1=CC=CC=C1 GZEXVQJHSUDDLU-UHFFFAOYSA-N 0.000 description 1
- RTAJXPNNTGBHNO-UHFFFAOYSA-N n-methyl-3-(methylamino)propanamide;hydrochloride Chemical compound Cl.CNCCC(=O)NC RTAJXPNNTGBHNO-UHFFFAOYSA-N 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 150000003891 oxalate salts Chemical class 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- NNFCIKHAZHQZJG-UHFFFAOYSA-N potassium cyanide Chemical compound [K+].N#[C-] NNFCIKHAZHQZJG-UHFFFAOYSA-N 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 239000000932 sedative agent Substances 0.000 description 1
- 230000001624 sedative effect Effects 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 239000000829 suppository Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 239000003826 tablet Substances 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
- 150000003892 tartrate salts Chemical class 0.000 description 1
- NRTLTGGGUQIRRT-UHFFFAOYSA-N triethylazanium;bromide Chemical compound [Br-].CC[NH+](CC)CC NRTLTGGGUQIRRT-UHFFFAOYSA-N 0.000 description 1
- ILWRPSCZWQJDMK-UHFFFAOYSA-N triethylazanium;chloride Chemical compound Cl.CCN(CC)CC ILWRPSCZWQJDMK-UHFFFAOYSA-N 0.000 description 1
- 229940099259 vaseline Drugs 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C255/00—Carboxylic acid nitriles
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2356239A DE2356239A1 (de) | 1973-11-10 | 1973-11-10 | Benzophenon-derivate und verfahren zu ihrer herstellung |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NO743980L true NO743980L (pt) | 1975-06-09 |
Family
ID=5897752
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO743980A NO743980L (pt) | 1973-11-10 | 1974-11-05 |
Country Status (24)
| Country | Link |
|---|---|
| US (1) | US4075409A (pt) |
| JP (1) | JPS5134136A (pt) |
| AR (4) | AR208184A1 (pt) |
| AT (4) | AT338246B (pt) |
| AU (1) | AU7505374A (pt) |
| BE (1) | BE821920R (pt) |
| CA (1) | CA1043348A (pt) |
| CH (4) | CH596149A5 (pt) |
| CS (4) | CS176288B2 (pt) |
| DD (1) | DD117068A6 (pt) |
| DE (1) | DE2356239A1 (pt) |
| DK (1) | DK575874A (pt) |
| ES (1) | ES431699A2 (pt) |
| FI (1) | FI322574A (pt) |
| FR (1) | FR2250522B2 (pt) |
| GB (1) | GB1441357A (pt) |
| HU (1) | HU170386B (pt) |
| IE (1) | IE40626B1 (pt) |
| NL (1) | NL7414419A (pt) |
| NO (1) | NO743980L (pt) |
| RO (4) | RO63798A7 (pt) |
| SE (1) | SE7413856L (pt) |
| SU (2) | SU520039A3 (pt) |
| ZA (1) | ZA747120B (pt) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SE384274B (sv) * | 1973-11-27 | 1976-04-26 | Stille Werner Ab | Serumseparator |
| JPS5651967Y2 (pt) * | 1977-04-18 | 1981-12-04 | ||
| FR2403330A1 (fr) * | 1977-06-16 | 1979-04-13 | Fabre Sa Pierre | Nouveaux derives de benzoyl-2-chloro-4-glycinanilides substitues, leur procede de preparation et leur application en tant que medicaments |
| FR2436776A1 (fr) * | 1978-09-25 | 1980-04-18 | Fabre Sa Pierre | Nouveaux derives d'ortho chloro benzoyl-2 chloro-4 glycylanilide, leur preparation et leur application en tant que medicaments |
| FR2459793A1 (fr) * | 1979-06-25 | 1981-01-16 | Fabre Sa Pierre | Nouveaux derives de benzoyl-2 nitro-4 anilides, leur preparation et leur application en tant que medicaments |
| JPH0465506U (pt) * | 1990-10-16 | 1992-06-08 | ||
| US5533518A (en) * | 1994-04-22 | 1996-07-09 | Becton, Dickinson And Company | Blood collection assembly including mechanical phase separating insert |
| US6723727B1 (en) * | 1996-12-20 | 2004-04-20 | Hoechst Aktiengesellschaft | Substituted purine derivatives, processes for their preparation, their use, and compositions comprising them |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| LU65340A1 (pt) * | 1972-05-12 | 1973-11-22 | ||
| US3928415A (en) * | 1973-05-08 | 1975-12-23 | Cassella Farbwerke Mainkur Ag | Benzophenone derivatives and process for their production II |
-
1973
- 1973-11-10 DE DE2356239A patent/DE2356239A1/de not_active Withdrawn
-
1974
- 1974-01-01 AR AR256421A patent/AR208184A1/es active
- 1974-01-01 AR AR256420A patent/AR208067A1/es active
- 1974-10-21 US US05/516,428 patent/US4075409A/en not_active Expired - Lifetime
- 1974-10-30 CA CA212,687A patent/CA1043348A/en not_active Expired
- 1974-11-01 CS CS7485A patent/CS176288B2/cs unknown
- 1974-11-01 CS CS7486A patent/CS176289B2/cs unknown
- 1974-11-01 CS CS7483A patent/CS176286B2/cs unknown
- 1974-11-01 CS CS7484A patent/CS176287B2/cs unknown
- 1974-11-05 AU AU75053/74A patent/AU7505374A/en not_active Expired
- 1974-11-05 NL NL7414419A patent/NL7414419A/xx not_active Application Discontinuation
- 1974-11-05 NO NO743980A patent/NO743980L/no unknown
- 1974-11-05 DK DK575874A patent/DK575874A/da unknown
- 1974-11-05 FI FI3225/74A patent/FI322574A/fi unknown
- 1974-11-05 SE SE7413856A patent/SE7413856L/xx not_active Application Discontinuation
- 1974-11-06 DD DD182200A patent/DD117068A6/xx unknown
- 1974-11-06 ES ES431699A patent/ES431699A2/es not_active Expired
- 1974-11-06 ZA ZA00747120A patent/ZA747120B/xx unknown
- 1974-11-06 CH CH1486074A patent/CH596149A5/xx not_active IP Right Cessation
- 1974-11-06 AR AR256419A patent/AR203127A1/es active
- 1974-11-06 RO RO7400083225A patent/RO63798A7/ro unknown
- 1974-11-06 GB GB4799374A patent/GB1441357A/en not_active Expired
- 1974-11-06 HU HUCA372A patent/HU170386B/hu unknown
- 1974-11-06 AT AT888674A patent/AT338246B/de not_active IP Right Cessation
- 1974-11-06 AT AT888974A patent/AT338248B/de not_active IP Right Cessation
- 1974-11-06 BE BE150274A patent/BE821920R/xx active
- 1974-11-06 RO RO7400083229A patent/RO63831A/ro unknown
- 1974-11-06 RO RO7400083228A patent/RO63793A/ro unknown
- 1974-11-06 CH CH1486274A patent/CH603554A5/xx not_active IP Right Cessation
- 1974-11-06 SU SU2073485A patent/SU520039A3/ru active
- 1974-11-06 AT AT888874A patent/AT343671B/de not_active IP Right Cessation
- 1974-11-06 CH CH1485974A patent/CH590211A5/xx not_active IP Right Cessation
- 1974-11-06 JP JP49127252A patent/JPS5134136A/ja active Pending
- 1974-11-06 RO RO7400080443A patent/RO64115A7/ro unknown
- 1974-11-06 IE IE2276/74A patent/IE40626B1/xx unknown
- 1974-11-06 CH CH1486174A patent/CH601203A5/xx not_active IP Right Cessation
- 1974-11-06 SU SU2072342A patent/SU521839A3/ru active
- 1974-11-06 AR AR256418A patent/AR203126A1/es active
- 1974-11-06 AT AT888774A patent/AT338247B/de not_active IP Right Cessation
- 1974-11-08 FR FR7437061A patent/FR2250522B2/fr not_active Expired
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US4244950A (en) | Derivatives of 4-amino-3-sulfonamido-pyridine, their preparation and use | |
| EP0104522B1 (en) | New pyrazolo(3,4-b)pyridine derivatives and process for producing them | |
| EP0074768A2 (en) | Alkanoylanilides | |
| JPS6053014B2 (ja) | 薬理作用を有するピリジン誘導体 | |
| NO743980L (pt) | ||
| AU764393B2 (en) | Pyridazin-3-one derivatives and medicines containing the same | |
| US4218476A (en) | Anti-thrombotic N-alkylthioakylamino benzenesulfonamides | |
| DK150511B (da) | Fremgangsmaade til fremstilling af 3,4-di-hydro-4-oxo-2h-1,2-benzothiazin-3-carboxamid-1,1-dioxid-forbindelser | |
| Aitland et al. | A facile synthesis of 2‐aminothiazolo [5, 4‐b]‐and 2‐aminothiazolo [4, 5‐c] pyridines | |
| NO803160L (no) | Pyrimidin-derivater. | |
| SU718011A3 (ru) | Способ получени производных 4-фенилтиено-(2,3-с)пиперидина или их солей | |
| McQuaid et al. | Substituted 5-amino-4, 5, 6, 7-tetrahydroindazoles as partial ergoline structures with dopaminergic activity | |
| GB2081261A (en) | Condensed as-triazine derivatives and process for preparing the same | |
| US6127362A (en) | 9,10-diazatricyclo[4,4,1,12,5 ] decane and 2,7-diazatricyclo [4,4,0,03,8 ] decane derivatives having analgesic activity | |
| US3983126A (en) | Aryloxy pyridine carboxylic-4-acids | |
| EP0393109B1 (en) | Novel 2,3-thiomorpholinedione-2-oxime derivatives, pharmaceutical compositions containing them and process for preparing same | |
| RU2032679C1 (ru) | Производные бензатиазинов | |
| EP0083566A1 (en) | Isoxazolyl indoles | |
| NO855210L (no) | Fremgangsmaate ved fremstilling av n-substituerte aziridin-2-carboxylsyrederivater. | |
| US3970650A (en) | Derivatives of tetralone and the preparation thereof | |
| US5169859A (en) | Thiazolidinone derivatives, pharmaceutical compositions containing them and process for preparing same | |
| US5142091A (en) | α, β-unsaturated ketones and ketoxime derivatives | |
| NO164845B (no) | Fremgangsmaate ved fremstilling av indanylderivater. | |
| US4482561A (en) | Therapeutically effective piperidyl N-(4-quinolyl)-anthraniloyloxyalkanoates | |
| US3642791A (en) | Morpholino-1-substituted-2(1h)-quinazolinones |