DD143520A5 - VERFAHREN ZUR HERSTELLUNG VON ALPHA-ECKIGE KLAMMER &UF4-(4-CHLORBENZOYLAMINOAETHYL)-PHENOXY ECKIGE KLAMMER ZU-2-METHYLPROPIONSAEURE - Google Patents
VERFAHREN ZUR HERSTELLUNG VON ALPHA-ECKIGE KLAMMER &UF4-(4-CHLORBENZOYLAMINOAETHYL)-PHENOXY ECKIGE KLAMMER ZU-2-METHYLPROPIONSAEURE Download PDFInfo
- Publication number
- DD143520A5 DD143520A5 DD79212723A DD21272379A DD143520A5 DD 143520 A5 DD143520 A5 DD 143520A5 DD 79212723 A DD79212723 A DD 79212723A DD 21272379 A DD21272379 A DD 21272379A DD 143520 A5 DD143520 A5 DD 143520A5
- Authority
- DD
- German Democratic Republic
- Prior art keywords
- phenoxy
- acid
- chlorobenzoyl
- tyramine
- chlorobenzoylaminoaethyl
- Prior art date
Links
- 238000004519 manufacturing process Methods 0.000 title abstract 2
- 239000002253 acid Substances 0.000 title description 3
- 150000007513 acids Chemical class 0.000 title 1
- 210000000078 claw Anatomy 0.000 title 1
- KHUXNRRPPZOJPT-UHFFFAOYSA-N phenoxy radical Chemical class O=C1C=C[CH]C=C1 KHUXNRRPPZOJPT-UHFFFAOYSA-N 0.000 title 1
- IIBYAHWJQTYFKB-UHFFFAOYSA-N bezafibrate Chemical compound C1=CC(OC(C)(C)C(O)=O)=CC=C1CCNC(=O)C1=CC=C(Cl)C=C1 IIBYAHWJQTYFKB-UHFFFAOYSA-N 0.000 claims abstract description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims description 28
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 claims description 24
- 101000588924 Anthopleura elegantissima Delta-actitoxin-Ael1a Proteins 0.000 claims description 8
- 238000000034 method Methods 0.000 claims description 8
- 238000002360 preparation method Methods 0.000 claims description 5
- 239000003513 alkali Substances 0.000 claims description 3
- -1 4-chlorobenzoylamino-ethyl Chemical group 0.000 abstract description 6
- KQNPFQTWMSNSAP-UHFFFAOYSA-N alpha-isobutyric acid Natural products CC(C)C(O)=O KQNPFQTWMSNSAP-UHFFFAOYSA-N 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 12
- HEMHJVSKTPXQMS-UHFFFAOYSA-M sodium hydroxide Inorganic materials [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 11
- 238000006243 chemical reaction Methods 0.000 description 9
- ZTLWJYCDAXUIBK-UHFFFAOYSA-N 4-chloro-n-[2-(4-hydroxyphenyl)ethyl]benzamide Chemical compound C1=CC(O)=CC=C1CCNC(=O)C1=CC=C(Cl)C=C1 ZTLWJYCDAXUIBK-UHFFFAOYSA-N 0.000 description 8
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 8
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 238000003756 stirring Methods 0.000 description 6
- 229960003732 tyramine Drugs 0.000 description 6
- DZGWFCGJZKJUFP-UHFFFAOYSA-N Tyramine Natural products NCCC1=CC=C(O)C=C1 DZGWFCGJZKJUFP-UHFFFAOYSA-N 0.000 description 5
- 150000002148 esters Chemical class 0.000 description 5
- DZGWFCGJZKJUFP-UHFFFAOYSA-O tyraminium Chemical compound [NH3+]CCC1=CC=C(O)C=C1 DZGWFCGJZKJUFP-UHFFFAOYSA-O 0.000 description 5
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 4
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 4
- 238000001816 cooling Methods 0.000 description 4
- XRHGYUZYPHTUJZ-UHFFFAOYSA-N 4-chlorobenzoic acid Chemical compound OC(=O)C1=CC=C(Cl)C=C1 XRHGYUZYPHTUJZ-UHFFFAOYSA-N 0.000 description 3
- RKIDDEGICSMIJA-UHFFFAOYSA-N 4-chlorobenzoyl chloride Chemical compound ClC(=O)C1=CC=C(Cl)C=C1 RKIDDEGICSMIJA-UHFFFAOYSA-N 0.000 description 3
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 3
- 239000007795 chemical reaction product Substances 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 239000012452 mother liquor Substances 0.000 description 3
- 238000001953 recrystallisation Methods 0.000 description 3
- 239000000725 suspension Substances 0.000 description 3
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 229910001854 alkali hydroxide Inorganic materials 0.000 description 2
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 2
- HVYWMOMLDIMFJA-DPAQBDIFSA-N cholesterol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CCCC(C)C)[C@@]1(C)CC2 HVYWMOMLDIMFJA-DPAQBDIFSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 230000035484 reaction time Effects 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- 229910000029 sodium carbonate Inorganic materials 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- 238000010626 work up procedure Methods 0.000 description 2
- ZOPSFRAJVKJCQG-UHFFFAOYSA-N 2,2-dichloro-3,3-dimethyloxirane Chemical compound CC1(C)OC1(Cl)Cl ZOPSFRAJVKJCQG-UHFFFAOYSA-N 0.000 description 1
- XXSPGBOGLXKMDU-UHFFFAOYSA-N 2-bromo-2-methylpropanoic acid Chemical compound CC(C)(Br)C(O)=O XXSPGBOGLXKMDU-UHFFFAOYSA-N 0.000 description 1
- BWLBGMIXKSTLSX-UHFFFAOYSA-N 2-hydroxyisobutyric acid Chemical compound CC(C)(O)C(O)=O BWLBGMIXKSTLSX-UHFFFAOYSA-N 0.000 description 1
- DDOGBPXNQPMRIK-UHFFFAOYSA-N 2-methylpropanoic acid;hydrobromide Chemical compound Br.CC(C)C(O)=O DDOGBPXNQPMRIK-UHFFFAOYSA-N 0.000 description 1
- 125000000242 4-chlorobenzoyl group Chemical group ClC1=CC=C(C(=O)*)C=C1 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 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
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- 229910052778 Plutonium Inorganic materials 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 239000003610 charcoal Substances 0.000 description 1
- 235000012000 cholesterol Nutrition 0.000 description 1
- 230000003670 easy-to-clean Effects 0.000 description 1
- 238000005265 energy consumption Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 230000017525 heat dissipation Effects 0.000 description 1
- 239000005457 ice water Substances 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 150000002632 lipids Chemical class 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 230000020477 pH reduction Effects 0.000 description 1
- OYEHPCDNVJXUIW-UHFFFAOYSA-N plutonium atom Chemical compound [Pu] OYEHPCDNVJXUIW-UHFFFAOYSA-N 0.000 description 1
- 239000002243 precursor Substances 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
- 238000004809 thin layer chromatography Methods 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C233/00—Carboxylic acid amides
- C07C233/01—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
- C07C233/12—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by halogen atoms or by nitro or nitroso groups
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/06—Antihyperlipidemics
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Obesity (AREA)
- Diabetes (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Hematology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (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 |
|---|---|---|---|
| DE2820759 | 1978-05-12 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DD143520A5 true DD143520A5 (de) | 1980-08-27 |
Family
ID=6039192
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DD79212723A DD143520A5 (de) | 1978-05-12 | 1979-05-08 | VERFAHREN ZUR HERSTELLUNG VON ALPHA-ECKIGE KLAMMER &UF4-(4-CHLORBENZOYLAMINOAETHYL)-PHENOXY ECKIGE KLAMMER ZU-2-METHYLPROPIONSAEURE |
Country Status (22)
| Country | Link |
|---|---|
| US (1) | US4370495A (cs) |
| JP (1) | JPS5649906B2 (cs) |
| AR (1) | AR219595A1 (cs) |
| AT (1) | AT365167B (cs) |
| AU (1) | AU520908B2 (cs) |
| BE (1) | BE876162A (cs) |
| CA (1) | CA1124260A (cs) |
| CH (1) | CH641762A5 (cs) |
| CS (1) | CS203960B2 (cs) |
| DD (1) | DD143520A5 (cs) |
| DK (1) | DK187579A (cs) |
| FI (1) | FI791466A7 (cs) |
| FR (1) | FR2425427B1 (cs) |
| GB (1) | GB2021575B (cs) |
| HU (1) | HU177958B (cs) |
| IL (1) | IL57220A (cs) |
| IT (1) | IT1166786B (cs) |
| NL (1) | NL183185C (cs) |
| PL (1) | PL114686B1 (cs) |
| SE (1) | SE433609B (cs) |
| SU (1) | SU828962A3 (cs) |
| YU (1) | YU41438B (cs) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| IL102707A (en) * | 1992-08-02 | 1996-11-14 | Cherkez Stephen | Processes for the preparation of tyramine derivatives |
| ATE157349T1 (de) * | 1993-05-12 | 1997-09-15 | Heumann Pharma Gmbh & Co | Stabile und kristalline form von bezafibrat |
| CN101353315B (zh) * | 2008-08-08 | 2011-05-11 | 淮阴工学院 | 一种苯扎贝特的制备方法 |
| CN101445467B (zh) * | 2008-12-30 | 2013-01-23 | 浙江九洲药业股份有限公司 | N-(4-氯苯甲酰基)-酪胺的化学合成方法 |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2108980A1 (en) * | 1970-10-27 | 1972-05-26 | Biosedra Lab | Pure ethyl alpha-p-iodophenoxyisobutyrate - with hypolipaemic activity |
| DE2230383C3 (de) * | 1971-10-01 | 1981-12-03 | Boehringer Mannheim Gmbh, 6800 Mannheim | Phenoxyalkylcarbonsäurederivate und Verfahren zur Herstellung derselben |
| US3948973A (en) * | 1972-08-29 | 1976-04-06 | Sterling Drug Inc. | Halocyclopropyl substituted phenoxyalkanoic acids |
| GB1422679A (en) * | 1972-11-16 | 1976-01-28 | Funai Pharmaceutical Ind Ltd | Substituted phenoxy-a-methylpropionic acid derivatives and a process for producing the same |
| JPS5735171B2 (cs) * | 1973-07-02 | 1982-07-27 | ||
| DE2405622A1 (de) * | 1974-02-06 | 1975-08-14 | Boehringer Mannheim Gmbh | Neue phenoxyalkylcarbonsaeurederivate und verfahren zur herstellung derselben |
| DE2541342A1 (de) * | 1975-09-17 | 1977-03-31 | Boehringer Mannheim Gmbh | Neue phenoxyalkylcarbonsaeuren und verfahren zur herstellung derselben |
-
1979
- 1979-04-13 JP JP4441079A patent/JPS5649906B2/ja not_active Expired
- 1979-04-17 US US06/030,798 patent/US4370495A/en not_active Expired - Lifetime
- 1979-04-30 CA CA326,593A patent/CA1124260A/en not_active Expired
- 1979-05-06 IL IL57220A patent/IL57220A/xx unknown
- 1979-05-07 FI FI791466A patent/FI791466A7/fi not_active Application Discontinuation
- 1979-05-07 AR AR276428A patent/AR219595A1/es active
- 1979-05-07 SU SU792761216A patent/SU828962A3/ru active
- 1979-05-07 DK DK187579A patent/DK187579A/da not_active Application Discontinuation
- 1979-05-08 PL PL1979215450A patent/PL114686B1/pl unknown
- 1979-05-08 DD DD79212723A patent/DD143520A5/de not_active IP Right Cessation
- 1979-05-08 SE SE7904008A patent/SE433609B/sv not_active IP Right Cessation
- 1979-05-08 IT IT22464/79A patent/IT1166786B/it active
- 1979-05-08 AU AU46790/79A patent/AU520908B2/en not_active Expired
- 1979-05-09 NL NLAANVRAGE7903631,A patent/NL183185C/xx not_active IP Right Cessation
- 1979-05-09 CH CH435079A patent/CH641762A5/de not_active IP Right Cessation
- 1979-05-09 GB GB7915965A patent/GB2021575B/en not_active Expired
- 1979-05-10 BE BE0/195085A patent/BE876162A/xx not_active IP Right Cessation
- 1979-05-10 YU YU1098/79A patent/YU41438B/xx unknown
- 1979-05-11 CS CS793234A patent/CS203960B2/cs unknown
- 1979-05-11 HU HU79BO1781A patent/HU177958B/hu unknown
- 1979-05-11 AT AT0352979A patent/AT365167B/de not_active IP Right Cessation
- 1979-05-11 FR FR7911966A patent/FR2425427B1/fr not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| DK187579A (da) | 1979-11-13 |
| US4370495A (en) | 1983-01-25 |
| IL57220A (en) | 1982-04-30 |
| SE433609B (sv) | 1984-06-04 |
| YU109879A (en) | 1982-10-31 |
| NL7903631A (nl) | 1979-11-14 |
| JPS5649906B2 (en) | 1981-11-25 |
| GB2021575A (en) | 1979-12-05 |
| IL57220A0 (en) | 1979-09-30 |
| SU828962A3 (ru) | 1981-05-07 |
| NL183185C (nl) | 1988-08-16 |
| AU520908B2 (en) | 1982-03-04 |
| GB2021575B (en) | 1982-07-07 |
| AT365167B (de) | 1981-12-28 |
| ATA352979A (de) | 1981-05-15 |
| AR219595A1 (es) | 1980-08-29 |
| AU4679079A (en) | 1979-11-15 |
| FI791466A7 (fi) | 1981-01-01 |
| IT7922464A0 (it) | 1979-05-08 |
| YU41438B (en) | 1987-06-30 |
| HU177958B (en) | 1982-02-28 |
| FR2425427A1 (fr) | 1979-12-07 |
| BE876162A (fr) | 1979-11-12 |
| PL114686B1 (en) | 1981-02-28 |
| CS203960B2 (en) | 1981-03-31 |
| IT1166786B (it) | 1987-05-06 |
| JPS54148742A (en) | 1979-11-21 |
| FR2425427B1 (fr) | 1984-08-24 |
| SE7904008L (sv) | 1979-11-13 |
| CA1124260A (en) | 1982-05-25 |
| CH641762A5 (de) | 1984-03-15 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| ENJ | Ceased due to non-payment of renewal fee |