NO134417B - - Google Patents
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- Publication number
- NO134417B NO134417B NO4256/71A NO425671A NO134417B NO 134417 B NO134417 B NO 134417B NO 4256/71 A NO4256/71 A NO 4256/71A NO 425671 A NO425671 A NO 425671A NO 134417 B NO134417 B NO 134417B
- Authority
- NO
- Norway
- Prior art keywords
- methoxy
- naphthyl
- acid
- propionic acid
- solution
- Prior art date
Links
- 239000011541 reaction mixture Substances 0.000 claims description 15
- 238000000034 method Methods 0.000 claims description 9
- 238000004519 manufacturing process Methods 0.000 claims description 6
- CMWTZPSULFXXJA-UHFFFAOYSA-N 2-(6-methoxy-2-naphthalenyl)propanoic acid Chemical compound C1=C(C(C)C(O)=O)C=CC2=CC(OC)=CC=C21 CMWTZPSULFXXJA-UHFFFAOYSA-N 0.000 claims description 5
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 claims description 5
- CMWTZPSULFXXJA-VIFPVBQESA-N naproxen Chemical compound C1=C([C@H](C)C(O)=O)C=CC2=CC(OC)=CC=C21 CMWTZPSULFXXJA-VIFPVBQESA-N 0.000 claims description 5
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 4
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 claims description 4
- 239000003960 organic solvent Substances 0.000 claims description 4
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims description 3
- VNDYJBBGRKZCSX-UHFFFAOYSA-L Zinc bromide Inorganic materials Br[Zn]Br VNDYJBBGRKZCSX-UHFFFAOYSA-L 0.000 claims description 3
- UAYWVJHJZHQCIE-UHFFFAOYSA-L Zinc iodide Inorganic materials I[Zn]I UAYWVJHJZHQCIE-UHFFFAOYSA-L 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
- 239000000460 chlorine Substances 0.000 claims description 3
- 229910052740 iodine Inorganic materials 0.000 claims description 3
- 239000011630 iodine Substances 0.000 claims description 3
- VHRRZJASORWNIU-UHFFFAOYSA-N zinc;6-methoxy-2h-naphthalen-2-ide Chemical compound [Zn+2].C1=[C-]C=CC2=CC(OC)=CC=C21.C1=[C-]C=CC2=CC(OC)=CC=C21 VHRRZJASORWNIU-UHFFFAOYSA-N 0.000 claims description 3
- CMWTZPSULFXXJA-UHFFFAOYSA-M 2-(6-methoxynaphthalen-2-yl)propanoate Chemical compound C1=C(C(C)C([O-])=O)C=CC2=CC(OC)=CC=C21 CMWTZPSULFXXJA-UHFFFAOYSA-M 0.000 claims description 2
- HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 claims description 2
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 2
- 125000004185 ester group Chemical group 0.000 claims description 2
- 235000019260 propionic acid Nutrition 0.000 claims description 2
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 claims description 2
- 229940102001 zinc bromide Drugs 0.000 claims description 2
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 claims 1
- VKYUFAYOVXNKFX-UHFFFAOYSA-M [Cl-].C1=C([Zn+])C=CC2=CC(OC)=CC=C21 Chemical compound [Cl-].C1=C([Zn+])C=CC2=CC(OC)=CC=C21 VKYUFAYOVXNKFX-UHFFFAOYSA-M 0.000 claims 1
- 125000005843 halogen group Chemical group 0.000 claims 1
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 33
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 33
- 239000000243 solution Substances 0.000 description 28
- 150000001875 compounds Chemical class 0.000 description 27
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 17
- 239000000203 mixture Substances 0.000 description 16
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 15
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 15
- 239000000047 product Substances 0.000 description 13
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 12
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 12
- 238000006243 chemical reaction Methods 0.000 description 11
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 10
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 10
- 238000003756 stirring Methods 0.000 description 9
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 8
- 239000002253 acid Substances 0.000 description 8
- -1 bromo- Chemical class 0.000 description 8
- 239000002904 solvent Substances 0.000 description 8
- JIAARYAFYJHUJI-UHFFFAOYSA-L zinc dichloride Chemical compound [Cl-].[Cl-].[Zn+2] JIAARYAFYJHUJI-UHFFFAOYSA-L 0.000 description 8
- 239000012074 organic phase Substances 0.000 description 7
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 6
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 6
- 125000000217 alkyl group Chemical group 0.000 description 6
- 230000007062 hydrolysis Effects 0.000 description 6
- 238000006460 hydrolysis reaction Methods 0.000 description 6
- 239000011777 magnesium Substances 0.000 description 6
- 229910052749 magnesium Inorganic materials 0.000 description 6
- 238000010992 reflux Methods 0.000 description 6
- AYFJBMBVXWNYLT-UHFFFAOYSA-N 2-bromo-6-methoxynaphthalene Chemical compound C1=C(Br)C=CC2=CC(OC)=CC=C21 AYFJBMBVXWNYLT-UHFFFAOYSA-N 0.000 description 5
- 229910052757 nitrogen Inorganic materials 0.000 description 5
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 5
- 229910052725 zinc Inorganic materials 0.000 description 5
- 239000011701 zinc Substances 0.000 description 5
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 4
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 4
- DMMNAMUAQVNNBC-UHFFFAOYSA-M magnesium;6-methoxy-2h-naphthalen-2-ide;bromide Chemical compound [Mg+2].[Br-].C1=[C-]C=CC2=CC(OC)=CC=C21 DMMNAMUAQVNNBC-UHFFFAOYSA-M 0.000 description 4
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 4
- KMPWYEUPVWOPIM-KODHJQJWSA-N cinchonidine Chemical compound C1=CC=C2C([C@H]([C@H]3[N@]4CC[C@H]([C@H](C4)C=C)C3)O)=CC=NC2=C1 KMPWYEUPVWOPIM-KODHJQJWSA-N 0.000 description 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 3
- 239000012299 nitrogen atmosphere Substances 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 239000002002 slurry Substances 0.000 description 3
- 239000011592 zinc chloride Substances 0.000 description 3
- 235000005074 zinc chloride Nutrition 0.000 description 3
- BMYNFMYTOJXKLE-UHFFFAOYSA-N 3-azaniumyl-2-hydroxypropanoate Chemical compound NCC(O)C(O)=O BMYNFMYTOJXKLE-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 2
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 2
- 239000008346 aqueous phase Substances 0.000 description 2
- NEHMKBQYUWJMIP-UHFFFAOYSA-N chloromethane Chemical compound ClC NEHMKBQYUWJMIP-UHFFFAOYSA-N 0.000 description 2
- KMPWYEUPVWOPIM-UHFFFAOYSA-N cinchonidine Natural products C1=CC=C2C(C(C3N4CCC(C(C4)C=C)C3)O)=CC=NC2=C1 KMPWYEUPVWOPIM-UHFFFAOYSA-N 0.000 description 2
- ARFLASKVLJTEJD-UHFFFAOYSA-N ethyl 2-bromopropanoate Chemical compound CCOC(=O)C(C)Br ARFLASKVLJTEJD-UHFFFAOYSA-N 0.000 description 2
- 239000000284 extract Substances 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- KDCIHNCMPUBDKT-UHFFFAOYSA-N hexane;propan-2-one Chemical compound CC(C)=O.CCCCCC KDCIHNCMPUBDKT-UHFFFAOYSA-N 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- 229940071870 hydroiodic acid Drugs 0.000 description 2
- 230000004968 inflammatory condition Effects 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- GBMDVOWEEQVZKZ-UHFFFAOYSA-N methanol;hydrate Chemical compound O.OC GBMDVOWEEQVZKZ-UHFFFAOYSA-N 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 230000035484 reaction time Effects 0.000 description 2
- HEMHJVSKTPXQMS-UHFFFAOYSA-M sodium hydroxide Inorganic materials [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- MONMFXREYOKQTI-UHFFFAOYSA-M 2-bromopropanoate Chemical compound CC(Br)C([O-])=O MONMFXREYOKQTI-UHFFFAOYSA-M 0.000 description 1
- 208000010392 Bone Fractures Diseases 0.000 description 1
- RDDCCFOINVFEPL-UHFFFAOYSA-N C1=C(OC)C=CC2=CC([Cd]C3=CC4=CC=C(C=C4C=C3)OC)=CC=C21 Chemical compound C1=C(OC)C=CC2=CC([Cd]C3=CC4=CC=C(C=C4C=C3)OC)=CC=C21 RDDCCFOINVFEPL-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- 206010010254 Concussion Diseases 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 description 1
- 201000005569 Gout Diseases 0.000 description 1
- 238000003747 Grignard reaction Methods 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
- 206010061218 Inflammation Diseases 0.000 description 1
- 241000124008 Mammalia Species 0.000 description 1
- 208000006670 Multiple fractures Diseases 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
- 208000010040 Sprains and Strains Diseases 0.000 description 1
- DHXVGJBLRPWPCS-UHFFFAOYSA-N Tetrahydropyran Chemical compound C1CCOCC1 DHXVGJBLRPWPCS-UHFFFAOYSA-N 0.000 description 1
- 208000025865 Ulcer Diseases 0.000 description 1
- 208000027418 Wounds and injury Diseases 0.000 description 1
- ZSDUBIPPXKBMQS-UHFFFAOYSA-M [Br-].C1=C([Zn+])C=CC2=CC(OC)=CC=C21 Chemical compound [Br-].C1=C([Zn+])C=CC2=CC(OC)=CC=C21 ZSDUBIPPXKBMQS-UHFFFAOYSA-M 0.000 description 1
- PGTXKIZLOWULDJ-UHFFFAOYSA-N [Mg].[Zn] Chemical group [Mg].[Zn] PGTXKIZLOWULDJ-UHFFFAOYSA-N 0.000 description 1
- 238000005903 acid hydrolysis reaction Methods 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000005215 alkyl ethers Chemical class 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 230000000202 analgesic effect Effects 0.000 description 1
- 230000003110 anti-inflammatory effect Effects 0.000 description 1
- 230000001754 anti-pyretic effect Effects 0.000 description 1
- 239000011260 aqueous acid Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 206010003246 arthritis Diseases 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 125000001246 bromo group Chemical group Br* 0.000 description 1
- INMAEXGIVZJYIJ-UHFFFAOYSA-N butyl 2-bromopropanoate Chemical compound CCCCOC(=O)C(C)Br INMAEXGIVZJYIJ-UHFFFAOYSA-N 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 150000001805 chlorine compounds Chemical class 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
- 238000003776 cleavage reaction Methods 0.000 description 1
- 230000009514 concussion Effects 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 239000008367 deionised water Substances 0.000 description 1
- 229910021641 deionized water Inorganic materials 0.000 description 1
- 239000000539 dimer Substances 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 238000010931 ester hydrolysis Methods 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- URNAYRDBUUZOIU-UHFFFAOYSA-N ethyl 2-(6-methoxynaphthalen-2-yl)propanoate Chemical compound C1=C(OC)C=CC2=CC(C(C)C(=O)OCC)=CC=C21 URNAYRDBUUZOIU-UHFFFAOYSA-N 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 239000012065 filter cake Substances 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 238000001640 fractional crystallisation Methods 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- CVIVDRZPZOBMDR-UHFFFAOYSA-N hexyl 2-bromopropanoate Chemical compound CCCCCCOC(=O)C(C)Br CVIVDRZPZOBMDR-UHFFFAOYSA-N 0.000 description 1
- 229940088597 hormone Drugs 0.000 description 1
- 239000005556 hormone Substances 0.000 description 1
- 230000004054 inflammatory process Effects 0.000 description 1
- 208000014674 injury Diseases 0.000 description 1
- 125000002346 iodo group Chemical group I* 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- ACEONLNNWKIPTM-UHFFFAOYSA-N methyl 2-bromopropanoate Chemical compound COC(=O)C(C)Br ACEONLNNWKIPTM-UHFFFAOYSA-N 0.000 description 1
- 229940050176 methyl chloride Drugs 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 210000002346 musculoskeletal system Anatomy 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 description 1
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- ODCLWDCSAGRHKS-UHFFFAOYSA-N propan-2-yl 2-bromopropanoate Chemical compound CC(C)OC(=O)C(C)Br ODCLWDCSAGRHKS-UHFFFAOYSA-N 0.000 description 1
- GDPGCHFFZZXKTQ-UHFFFAOYSA-N propyl 2-bromopropanoate Chemical compound CCCOC(=O)C(C)Br GDPGCHFFZZXKTQ-UHFFFAOYSA-N 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000012264 purified product Substances 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 230000007017 scission Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- CVAWKJKISIPBOD-UHFFFAOYSA-N tert-butyl 2-bromopropanoate Chemical compound CC(Br)C(=O)OC(C)(C)C CVAWKJKISIPBOD-UHFFFAOYSA-N 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 210000001519 tissue Anatomy 0.000 description 1
- 231100000397 ulcer Toxicity 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 150000003752 zinc compounds Chemical class 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F3/00—Compounds containing elements of Groups 2 or 12 of the Periodic Table
- C07F3/02—Magnesium compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F3/00—Compounds containing elements of Groups 2 or 12 of the Periodic Table
- C07F3/06—Zinc compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| NO210972A NO136199C (no) | 1970-12-04 | 1972-06-14 | Forbindelser for bruk som mellomprodukter ved fremstilling av 2-(6-metoksy-2-naftyl)propionsyre. |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US9537770A | 1970-12-04 | 1970-12-04 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| NO134417B true NO134417B (ru) | 1976-06-28 |
| NO134417C NO134417C (ru) | 1976-10-06 |
Family
ID=22251663
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO4256/71A NO134417C (ru) | 1970-12-04 | 1971-11-18 |
Country Status (23)
| Country | Link |
|---|---|
| US (1) | US3663584A (ru) |
| JP (1) | JPS5411304B1 (ru) |
| AT (1) | AT312584B (ru) |
| AU (1) | AU454101B2 (ru) |
| CA (1) | CA1020575A (ru) |
| CH (1) | CH559163A5 (ru) |
| CS (1) | CS168574B2 (ru) |
| DE (1) | DE2159011C3 (ru) |
| DK (1) | DK139962B (ru) |
| ES (1) | ES397591A1 (ru) |
| FI (1) | FI55985C (ru) |
| FR (1) | FR2116495B1 (ru) |
| GB (1) | GB1321347A (ru) |
| HU (1) | HU162870B (ru) |
| IL (1) | IL37972A (ru) |
| IT (1) | IT1182250B (ru) |
| NL (1) | NL168820C (ru) |
| NO (1) | NO134417C (ru) |
| PH (1) | PH10254A (ru) |
| SE (2) | SE385118B (ru) |
| SU (1) | SU571186A3 (ru) |
| YU (1) | YU35865B (ru) |
| ZA (1) | ZA716993B (ru) |
Families Citing this family (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3904682A (en) * | 1967-01-13 | 1975-09-09 | Syntex Corp | 2-(6{40 -Methoxy-2{40 -naphthyl)acetic acid |
| US4009197A (en) * | 1967-01-13 | 1977-02-22 | Syntex Corporation | 2-(6-Substituted-2'-naphthyl) acetic acid derivatives and the salts and esters thereof |
| US3998966A (en) * | 1971-11-04 | 1976-12-21 | Syntex Corporation | Anti-inflammatory, analgesic, anti-pyretic and anti-pruritic 6-substituted 2-naphthyl acetic acid derivative-containing compositions and methods of use thereof |
| US3975432A (en) * | 1972-03-16 | 1976-08-17 | Syntex Corporation | Process for preparing 2-(6-methoxy-2-naphthyl)propionic acid |
| US4033816A (en) * | 1973-06-18 | 1977-07-05 | The Upjohn Company | Process for inhibiting platelet aggregation |
| JPS57156434A (en) * | 1981-03-19 | 1982-09-27 | Takeda Chem Ind Ltd | Zinc indanecarboxylate |
| US4395571A (en) * | 1982-06-03 | 1983-07-26 | Syntex (U.S.A.) Inc. | Process for the preparation of d,1-2-(6-methoxy-2-naphthyl)propionic acid |
| US4723033A (en) * | 1982-11-24 | 1988-02-02 | Syntex Pharmaceuticals International Ltd. | Manufacture of optically active α-arylalkanoic acids and precursors thereof |
| JPS6081145A (ja) * | 1983-10-11 | 1985-05-09 | Nissan Chem Ind Ltd | ｄ−α−（６−メトキシ−２−ナフチル）プロピオン酸エステルのアルカリ性加水分解による，ｄ−α−（６−メトキシ−２−ナフチル）プロピオン酸の製法 |
| DE3345660A1 (de) * | 1983-12-16 | 1985-06-27 | Boehringer Mannheim Gmbh, 6800 Mannheim | Verfahren zur gewinnung von d(+)naproxen |
| EP0231257A1 (en) * | 1985-07-12 | 1987-08-12 | The Upjohn Company | Chemical compounds comrpising substituted phenylrings |
| US5049685A (en) * | 1988-11-22 | 1991-09-17 | Sanko Kaihatsu Kagaku Kenkyusho | Nuclear substituted salicylic acids and their salts |
| KR930003864B1 (ko) * | 1990-10-19 | 1993-05-14 | 한국과학기술연구원 | d-2-(6-메톡시-2-나프틸)-프로피온산의 제조방법 |
| US5179208A (en) * | 1990-10-19 | 1993-01-12 | Korea Institute Of Science And Technology | Process for preparing d-2-(6-methoxy-2-naphthyl)-propionic acid and intermediate thereof |
| US5750764A (en) * | 1995-11-17 | 1998-05-12 | Aeci Limited | Synthesis and resolution of propionic acid derivatives |
| US6080888A (en) * | 1997-01-08 | 2000-06-27 | Albemarle Corporation | Preparation of olefinic compounds and carboxylic derivatives thereof |
| US5792886A (en) * | 1997-01-08 | 1998-08-11 | Albemarle Corporation | Production of racemic 2-(6-methoxy-2-naphthyl) propionic acid of precursors thereof |
| US6096920A (en) * | 1997-01-08 | 2000-08-01 | Albemarle Corporation | Preparation of carboxylic compounds and their derivatives |
| EP2155759A4 (en) * | 2007-05-07 | 2012-10-17 | Valorisation Rech Soc En Commandite | METHODS FOR THE PREPARATION OF DIORGANOZINC COMPOUNDS |
| CN101412670B (zh) * | 2007-10-19 | 2011-11-09 | 浙江普洛医药科技有限公司 | 洛索洛芬钠的合成方法 |
| US8779200B2 (en) | 2009-02-25 | 2014-07-15 | Council Of Scientific & Industrial Research | Microwave induced single step green synthesis of some novel 2-aryl aldehydes and their analogues |
-
1970
- 1970-12-04 US US95377A patent/US3663584A/en not_active Expired - Lifetime
-
1971
- 1971-10-19 ZA ZA716993A patent/ZA716993B/xx unknown
- 1971-10-20 IL IL37972A patent/IL37972A/xx unknown
- 1971-10-20 CA CA125,589A patent/CA1020575A/en not_active Expired
- 1971-10-26 FI FI3029/71A patent/FI55985C/fi active
- 1971-11-03 NL NLAANVRAGE7115162,A patent/NL168820C/xx not_active IP Right Cessation
- 1971-11-08 IT IT70654/71A patent/IT1182250B/it active
- 1971-11-09 DK DK547771AA patent/DK139962B/da not_active IP Right Cessation
- 1971-11-18 AU AU35863/71A patent/AU454101B2/en not_active Expired
- 1971-11-18 NO NO4256/71A patent/NO134417C/no unknown
- 1971-11-18 JP JP9270171A patent/JPS5411304B1/ja active Pending
- 1971-11-18 CS CS8070*BA patent/CS168574B2/cs unknown
- 1971-11-25 AT AT1015771A patent/AT312584B/de active
- 1971-11-25 CH CH1715371A patent/CH559163A5/xx not_active IP Right Cessation
- 1971-11-29 DE DE2159011A patent/DE2159011C3/de not_active Expired
- 1971-11-29 GB GB5537871A patent/GB1321347A/en not_active Expired
- 1971-11-29 SU SU7101719843A patent/SU571186A3/ru active
- 1971-12-02 YU YU3036/71A patent/YU35865B/xx unknown
- 1971-12-02 FR FR7143294A patent/FR2116495B1/fr not_active Expired
- 1971-12-02 ES ES397591A patent/ES397591A1/es not_active Expired
- 1971-12-03 HU HUSI1239A patent/HU162870B/hu unknown
- 1971-12-03 SE SE7115548A patent/SE385118B/xx unknown
-
1974
- 1974-01-17 PH PH15425*A patent/PH10254A/en unknown
- 1974-09-16 SE SE7411643A patent/SE402109B/xx not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| ES397591A1 (es) | 1974-06-16 |
| CA1020575A (en) | 1977-11-08 |
| IT1182250B (it) | 1987-09-30 |
| GB1321347A (en) | 1973-06-27 |
| SE385118B (sv) | 1976-06-08 |
| FR2116495B1 (ru) | 1974-09-06 |
| DE2159011A1 (de) | 1972-06-08 |
| FI55985C (fi) | 1979-11-12 |
| ZA716993B (en) | 1973-06-27 |
| SE7411643L (ru) | 1974-09-16 |
| CS168574B2 (ru) | 1976-06-29 |
| DE2159011B2 (de) | 1980-11-27 |
| CH559163A5 (ru) | 1975-02-28 |
| AT312584B (de) | 1974-01-10 |
| YU303671A (en) | 1981-02-28 |
| JPS5411304B1 (ru) | 1979-05-14 |
| NL168820B (nl) | 1981-12-16 |
| SU571186A3 (ru) | 1977-08-30 |
| IL37972A0 (en) | 1971-12-29 |
| AU454101B2 (en) | 1974-09-25 |
| AU3586371A (en) | 1973-05-24 |
| DK139962B (da) | 1979-05-28 |
| US3663584A (en) | 1972-05-16 |
| NL7115162A (ru) | 1972-06-06 |
| PH10254A (en) | 1976-10-14 |
| DK139962C (ru) | 1979-11-12 |
| NL168820C (nl) | 1982-05-17 |
| IL37972A (en) | 1974-12-31 |
| HU162870B (ru) | 1973-04-28 |
| FR2116495A1 (ru) | 1972-07-13 |
| FI55985B (fi) | 1979-07-31 |
| YU35865B (en) | 1981-08-31 |
| SE402109B (sv) | 1978-06-19 |
| NO134417C (ru) | 1976-10-06 |
| DE2159011C3 (de) | 1981-09-17 |
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