DD142053A5 - Verfahren zur herstellung von neuen thieno eckige klammer auf 3,2-c eckige klammer zu-und thieno eckige klammer auf 2,3-c eckige klammer zu pyridinen - Google Patents
Verfahren zur herstellung von neuen thieno eckige klammer auf 3,2-c eckige klammer zu-und thieno eckige klammer auf 2,3-c eckige klammer zu pyridinen Download PDFInfo
- Publication number
- DD142053A5 DD142053A5 DD79211045A DD21104579A DD142053A5 DD 142053 A5 DD142053 A5 DD 142053A5 DD 79211045 A DD79211045 A DD 79211045A DD 21104579 A DD21104579 A DD 21104579A DD 142053 A5 DD142053 A5 DD 142053A5
- Authority
- DD
- German Democratic Republic
- Prior art keywords
- derivative
- alkyl
- pyridine
- bracket
- yield
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 50
- RQMWVVBHJMUJNZ-UHFFFAOYSA-N 4-chloropyridin-2-amine Chemical compound NC1=CC(Cl)=CC=N1 RQMWVVBHJMUJNZ-UHFFFAOYSA-N 0.000 title 1
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- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 239000000829 suppository Substances 0.000 description 1
- 208000011580 syndromic disease Diseases 0.000 description 1
- 239000006188 syrup Substances 0.000 description 1
- 235000020357 syrup Nutrition 0.000 description 1
- 239000003826 tablet Substances 0.000 description 1
- 229940124597 therapeutic agent Drugs 0.000 description 1
- GHYPQAOXZUEFNP-UHFFFAOYSA-N thieno[2,3-c]pyridine-2-carboxylic acid Chemical compound C1=NC=C2SC(C(=O)O)=CC2=C1 GHYPQAOXZUEFNP-UHFFFAOYSA-N 0.000 description 1
- SJOJSVUJOMBMRX-UHFFFAOYSA-N thieno[3,2-c]pyridine-6-carboxylic acid Chemical compound C1=NC(C(=O)O)=CC2=C1C=CS2 SJOJSVUJOMBMRX-UHFFFAOYSA-N 0.000 description 1
- 230000001256 tonic effect Effects 0.000 description 1
- 230000000472 traumatic effect Effects 0.000 description 1
- 150000003626 triacylglycerols Chemical class 0.000 description 1
- 230000002618 waking effect Effects 0.000 description 1
- 229940045860 white wax Drugs 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D495/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/08—Antiepileptics; Anticonvulsants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/20—Hypnotics; Sedatives
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pain & Pain Management (AREA)
- Biomedical Technology (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Anesthesiology (AREA)
- Rheumatology (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR7804561A FR2417512A1 (fr) | 1978-02-17 | 1978-02-17 | Thieno (3,2-c) et thieno (2,3-c) pyridines, leur procede de preparation et leur application en therapeutique |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DD142053A5 true DD142053A5 (de) | 1980-06-04 |
Family
ID=9204729
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DD79211045A DD142053A5 (de) | 1978-02-17 | 1979-02-15 | Verfahren zur herstellung von neuen thieno eckige klammer auf 3,2-c eckige klammer zu-und thieno eckige klammer auf 2,3-c eckige klammer zu pyridinen |
Country Status (31)
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2525595A1 (fr) * | 1982-04-27 | 1983-10-28 | Pharmuka Lab | Nouveaux derives d'arene et d'heteroarenecarboxamides et leur utilisation comme medicaments |
| DE3621413A1 (de) * | 1986-06-26 | 1988-01-07 | Boehringer Ingelheim Kg | Verwendung carbocyclisch und heterocyclisch annelierter dihydropyridine als cardioprotektive mittel sowie neue heterocyclisch und carbocyclisch anellierte dihydropyridine, verfahren zu deren herstellung und zwischenstufen fuer deren herstellung |
| WO1988002751A1 (en) * | 1986-10-13 | 1988-04-21 | Asahi Kasei Kogyo Kabushiki Kaisha | Pyridine derivatives |
| WO2009037570A2 (en) * | 2007-08-10 | 2009-03-26 | Crystalgenomics, Inc. | Pyridine derivatives and methods of use thereof |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3845065A (en) * | 1972-02-18 | 1974-10-29 | Merck & Co Inc | 4-oxo-4,5-dihydrothieno(3,2-c)pyridines |
-
1978
- 1978-02-17 FR FR7804561A patent/FR2417512A1/fr active Granted
-
1979
- 1979-01-26 DE DE7979400053T patent/DE2960109D1/de not_active Expired
- 1979-01-26 EP EP79400053A patent/EP0003920B1/fr not_active Expired
- 1979-01-29 CH CH84479A patent/CH635844A5/fr not_active IP Right Cessation
- 1979-01-30 IE IE163/79A patent/IE47789B1/en not_active IP Right Cessation
- 1979-01-30 GR GR58210A patent/GR66844B/el unknown
- 1979-01-30 IL IL56541A patent/IL56541A/xx unknown
- 1979-01-31 LU LU80861A patent/LU80861A1/xx unknown
- 1979-02-02 ES ES477401A patent/ES477401A1/es not_active Expired
- 1979-02-02 AU AU43897/79A patent/AU519318B2/en not_active Ceased
- 1979-02-06 ZA ZA79513A patent/ZA79513B/xx unknown
- 1979-02-07 DK DK50279A patent/DK146046C/da not_active IP Right Cessation
- 1979-02-07 YU YU00268/79A patent/YU26879A/xx unknown
- 1979-02-07 AR AR275419A patent/AR227623A1/es active
- 1979-02-09 AT AT0098679A patent/AT369369B/de not_active IP Right Cessation
- 1979-02-09 RO RO7996565A patent/RO76642A/ro unknown
- 1979-02-12 FI FI790460A patent/FI66872C/fi not_active IP Right Cessation
- 1979-02-13 PT PT7969220A patent/PT69220A/pt unknown
- 1979-02-13 CA CA321,393A patent/CA1126732A/en not_active Expired
- 1979-02-13 NZ NZ189638A patent/NZ189638A/xx unknown
- 1979-02-14 HU HU79PA1342A patent/HU178075B/hu not_active IP Right Cessation
- 1979-02-15 IT IT48023/79A patent/IT1115001B/it active
- 1979-02-15 DD DD79211045A patent/DD142053A5/de not_active IP Right Cessation
- 1979-02-15 MX MX797720U patent/MX5588E/es unknown
- 1979-02-16 PH PH22206A patent/PH15171A/en unknown
- 1979-02-16 NO NO790515A patent/NO150483C/no unknown
- 1979-02-16 BE BE0/193507A patent/BE874228A/xx not_active IP Right Cessation
- 1979-02-16 SU SU792728455A patent/SU810081A3/ru active
- 1979-02-16 PL PL1979213472A patent/PL117264B1/pl unknown
- 1979-02-16 GB GB7905508A patent/GB2014576B/en not_active Expired
- 1979-02-17 JP JP1778479A patent/JPS54157599A/ja active Granted
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PJ | Ceased due to non-payment of renewal fee (addendum to changes before extension act) |