NO750412L - - Google Patents
Info
- Publication number
- NO750412L NO750412L NO750412A NO750412A NO750412L NO 750412 L NO750412 L NO 750412L NO 750412 A NO750412 A NO 750412A NO 750412 A NO750412 A NO 750412A NO 750412 L NO750412 L NO 750412L
- Authority
- NO
- Norway
- Prior art keywords
- formula
- compounds
- biphenylyl
- ethyl ester
- stands
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 claims description 49
- 238000000034 method Methods 0.000 claims description 18
- 239000001257 hydrogen Substances 0.000 claims description 11
- 229910052739 hydrogen Inorganic materials 0.000 claims description 11
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 7
- 125000000217 alkyl group Chemical group 0.000 claims description 7
- 125000004432 carbon atom Chemical group C* 0.000 claims description 7
- 239000002253 acid Substances 0.000 claims description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 5
- 239000000010 aprotic solvent Substances 0.000 claims description 4
- 150000002431 hydrogen Chemical class 0.000 claims description 4
- 239000007795 chemical reaction product Substances 0.000 claims description 3
- 238000002360 preparation method Methods 0.000 claims description 3
- 125000003545 alkoxy group Chemical group 0.000 claims description 2
- 230000008030 elimination Effects 0.000 claims description 2
- 238000003379 elimination reaction Methods 0.000 claims description 2
- 125000004429 atom Chemical group 0.000 claims 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 20
- 239000000203 mixture Substances 0.000 description 12
- 239000000243 solution Substances 0.000 description 8
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 7
- -1 tetrahydrofuran Chemical class 0.000 description 7
- RTCKPJQCILDACJ-UHFFFAOYSA-N C(C)OC(CC(=C)C1=C(C=CC=C1)C1=CC=CC=C1)=O Chemical compound C(C)OC(CC(=C)C1=C(C=CC=C1)C1=CC=CC=C1)=O RTCKPJQCILDACJ-UHFFFAOYSA-N 0.000 description 6
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 6
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 6
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 6
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 4
- 230000007062 hydrolysis Effects 0.000 description 4
- 238000006460 hydrolysis reaction Methods 0.000 description 4
- 238000002844 melting Methods 0.000 description 4
- 230000008018 melting Effects 0.000 description 4
- 150000003839 salts Chemical class 0.000 description 4
- 239000007858 starting material Substances 0.000 description 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- QIEPRFVBOFBFLG-UHFFFAOYSA-N ethyl 3-(2-phenylphenyl)but-2-enoate Chemical compound CCOC(=O)C=C(C)C1=CC=CC=C1C1=CC=CC=C1 QIEPRFVBOFBFLG-UHFFFAOYSA-N 0.000 description 3
- 239000000155 melt Substances 0.000 description 3
- 239000012074 organic phase Substances 0.000 description 3
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 3
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
- 241000700159 Rattus Species 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 239000000908 ammonium hydroxide Substances 0.000 description 2
- 239000008346 aqueous phase Substances 0.000 description 2
- 239000002585 base Substances 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- KDPAWGWELVVRCH-UHFFFAOYSA-M bromoacetate Chemical compound [O-]C(=O)CBr KDPAWGWELVVRCH-UHFFFAOYSA-M 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- KQGYHGXOSLDDLK-UHFFFAOYSA-N ethyl 3-hydroxy-3-(2-phenylphenyl)butanoate Chemical compound CCOC(=O)CC(C)(O)C1=CC=CC=C1C1=CC=CC=C1 KQGYHGXOSLDDLK-UHFFFAOYSA-N 0.000 description 2
- 239000000706 filtrate Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 238000011065 in-situ storage Methods 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- 238000001953 recrystallisation Methods 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- HEMHJVSKTPXQMS-UHFFFAOYSA-M sodium hydroxide Inorganic materials [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 2
- WRECIMRULFAWHA-UHFFFAOYSA-N trimethyl borate Chemical compound COB(OC)OC WRECIMRULFAWHA-UHFFFAOYSA-N 0.000 description 2
- CSDQQAQKBAQLLE-UHFFFAOYSA-N 4-(4-chlorophenyl)-4,5,6,7-tetrahydrothieno[3,2-c]pyridine Chemical compound C1=CC(Cl)=CC=C1C1C(C=CS2)=C2CCN1 CSDQQAQKBAQLLE-UHFFFAOYSA-N 0.000 description 1
- 208000009386 Experimental Arthritis Diseases 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
- 241000186359 Mycobacterium Species 0.000 description 1
- 206010030113 Oedema Diseases 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical class CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 239000002671 adjuvant Substances 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 1
- 229940121363 anti-inflammatory agent Drugs 0.000 description 1
- 239000002260 anti-inflammatory agent Substances 0.000 description 1
- 230000003110 anti-inflammatory effect Effects 0.000 description 1
- 239000011260 aqueous acid Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000000679 carrageenan Substances 0.000 description 1
- 229940113118 carrageenan Drugs 0.000 description 1
- 235000010418 carrageenan Nutrition 0.000 description 1
- 229920001525 carrageenan Polymers 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000010411 cooking Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000002274 desiccant Substances 0.000 description 1
- 239000003480 eluent Substances 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- PQJJJMRNHATNKG-UHFFFAOYSA-N ethyl bromoacetate Chemical compound CCOC(=O)CBr PQJJJMRNHATNKG-UHFFFAOYSA-N 0.000 description 1
- 125000004494 ethyl ester group Chemical group 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 238000010575 fractional recrystallization Methods 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000002808 molecular sieve Substances 0.000 description 1
- 239000012452 mother liquor Substances 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 230000003285 pharmacodynamic effect Effects 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 238000007127 saponification reaction Methods 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 230000000707 stereoselective effect Effects 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 230000007306 turnover Effects 0.000 description 1
- 238000005292 vacuum distillation Methods 0.000 description 1
- 150000003751 zinc Chemical class 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- UHVMMEOXYDMDKI-JKYCWFKZSA-L zinc;1-(5-cyanopyridin-2-yl)-3-[(1s,2s)-2-(6-fluoro-2-hydroxy-3-propanoylphenyl)cyclopropyl]urea;diacetate Chemical compound [Zn+2].CC([O-])=O.CC([O-])=O.CCC(=O)C1=CC=C(F)C([C@H]2[C@H](C2)NC(=O)NC=2N=CC(=CC=2)C#N)=C1O UHVMMEOXYDMDKI-JKYCWFKZSA-L 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C57/00—Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms
- C07C57/30—Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms containing six-membered aromatic rings
- C07C57/42—Unsaturated compounds having carboxyl groups bound to acyclic carbon atoms containing six-membered aromatic rings having unsaturation outside the rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C59/00—Compounds having carboxyl groups bound to acyclic carbon atoms and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups
- C07C59/40—Unsaturated compounds
- C07C59/58—Unsaturated compounds containing ether groups, groups, groups, or groups
- C07C59/64—Unsaturated compounds containing ether groups, groups, groups, or groups containing six-membered aromatic rings
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)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US48442874A | 1974-07-01 | 1974-07-01 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NO750412L true NO750412L (xx) | 1976-01-05 |
Family
ID=23924138
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO750412A NO750412L (xx) | 1974-07-01 | 1975-02-10 |
Country Status (12)
| Country | Link |
|---|---|
| JP (1) | JPS518250A (xx) |
| BE (1) | BE825643A (xx) |
| DD (1) | DD118859A5 (xx) |
| DE (1) | DE2505446A1 (xx) |
| DK (1) | DK48675A (xx) |
| FI (1) | FI750356A (xx) |
| FR (1) | FR2276817A1 (xx) |
| IL (1) | IL46642A0 (xx) |
| NL (1) | NL7501739A (xx) |
| NO (1) | NO750412L (xx) |
| SE (1) | SE7501444L (xx) |
| ZA (1) | ZA75974B (xx) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS588375B2 (ja) * | 1976-02-05 | 1983-02-15 | 日清製粉株式会社 | プロピオン酸誘導体化合物 |
| JPS5386364A (en) * | 1976-12-28 | 1978-07-29 | Hirose Masayuki | Soil conditioning method |
| JPS5392514A (en) * | 1977-01-24 | 1978-08-14 | Dai Ichi Kogyo Seiyaku Co Ltd | Method of improving weak ground |
| US4453005A (en) * | 1982-12-06 | 1984-06-05 | Merck Frosst Canada, Inc. | Process for preparing substituted phenylalkenoic acids |
| US4536515A (en) * | 1982-12-06 | 1985-08-20 | Merck Frosst Canada, Inc. | Substituted phenylalkenoic acids and esters |
| JPH0691999B2 (ja) * | 1989-01-24 | 1994-11-16 | ハイモ株式会社 | 含水掘削残土の処理方法 |
| JP2529785B2 (ja) * | 1991-05-22 | 1996-09-04 | 三菱化学株式会社 | 含水土壌の改良剤 |
-
1975
- 1975-02-10 SE SE7501444A patent/SE7501444L/xx unknown
- 1975-02-10 FI FI750356A patent/FI750356A/fi not_active Application Discontinuation
- 1975-02-10 DE DE19752505446 patent/DE2505446A1/de active Pending
- 1975-02-10 DK DK48675*#A patent/DK48675A/da unknown
- 1975-02-10 NO NO750412A patent/NO750412L/no unknown
- 1975-02-14 NL NL7501739A patent/NL7501739A/xx unknown
- 1975-02-17 DD DD184256A patent/DD118859A5/xx unknown
- 1975-02-17 BE BE153448A patent/BE825643A/xx unknown
- 1975-02-17 ZA ZA00750974A patent/ZA75974B/xx unknown
- 1975-02-17 JP JP50018957A patent/JPS518250A/ja active Pending
- 1975-02-17 IL IL46642A patent/IL46642A0/xx unknown
- 1975-02-18 FR FR7504949A patent/FR2276817A1/fr not_active Withdrawn
Also Published As
| Publication number | Publication date |
|---|---|
| DE2505446A1 (de) | 1976-01-22 |
| DK48675A (da) | 1976-01-02 |
| NL7501739A (nl) | 1976-01-05 |
| FR2276817A1 (fr) | 1976-01-30 |
| BE825643A (fr) | 1975-08-18 |
| IL46642A0 (en) | 1975-04-25 |
| ZA75974B (en) | 1976-09-29 |
| FI750356A (xx) | 1976-01-02 |
| JPS518250A (xx) | 1976-01-23 |
| SE7501444L (sv) | 1976-01-02 |
| DD118859A5 (xx) | 1976-03-20 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| NO750412L (xx) | ||
| SU479290A3 (ru) | Способ получени 2-(фурилметил)-6,7бензоморфанов | |
| Paquette et al. | . alpha.-Halo sulfones. VI. Evidence for the intermediacy of thiirene dioxides in the base-promoted rearrangement of. alpha.,. alpha.-dichloro sulfones | |
| Berson et al. | The Synthesis and Complete Resolution of 2-Hydroxy-1, 1'-binaphthyl and the Reaction of its Phenylglyoxylate with Methylmagnesium Iodide1, 2 | |
| JPH0627098B2 (ja) | セルトラリン中間体の製造方法 | |
| SU649311A3 (ru) | Способ получени алкилпроизводных простановой кислоты | |
| Campaigne et al. | Synthesis of β-Dimethylaminoethyl and α-Hydroxy-β-Dimethylaminoethyl Derivatives from Organolithium Compounds and Tetramethyoxamide | |
| Gardner et al. | 3, 7-Dicarbethoxy-5-hydroxytropolone. A Convenient Synthesis of Pimelic Acid1 | |
| GB2185743A (en) | 8 alpha -Acylaminoergoline's | |
| NO761142L (xx) | ||
| NO144884B (no) | Fremgangsmaate til fremstilling av optisk aktive lavere alkyl-imiedazolkarboksylater | |
| Hirao et al. | Fluoroalkylnorbornadienes and their corresponding valence isomer quadricyclanes—a light energy storage system | |
| US3281469A (en) | Process for preparing 5-hydroxy-5-(3-aminoalkynyl) dibenzo [a, d] cyclohepta [1, 4] denes | |
| US2895927A (en) | Synthesis of thyronine compounds | |
| US3538227A (en) | Tricyclic phenoxy-acid and ester hypocholesterolemic compositions | |
| CN117447355B (zh) | 一种米洛巴林中间体的制备方法 | |
| US2649449A (en) | 2-cyclohexylamino-4-amino-5-benzylpyrimidine | |
| US3321535A (en) | Process for dibenzo[a, d]cyclohepta[1.4]diene intermediates | |
| IE45345B1 (en) | Procress for preparing an acetonitrile derivative | |
| US3019233A (en) | 5-hydroxy-2-oxyphenylcyclopentane-alkanols and intermediates | |
| Fringuelli et al. | Heteroaromatic rings as substituents. Part 5. Evaluation of σ and σ–constants of 2-selenienyl and 2-tellurienyl groups | |
| US4906765A (en) | Process for the production of 4-alkoxy-2(5H) thiophenones | |
| JPS5953256B2 (ja) | α↑１−ｔｅｒｔ．−ブチルアミノメチル−４−ヒドロキシ−ｍ−キシレン−α↑１，α↑３−ジオ−ルの製造法 | |
| Brown et al. | Aspects of isocoumarin chemistry. Part I. A synthesis of berbine derivatives | |
| Lambert et al. | The. zeta.(Zeta) effect of tin |