SU1022659A3 - Способ получени производных пиридо (1,2- @ ) пиримидина или их кислотно-аддитивных солей - Google Patents
Способ получени производных пиридо (1,2- @ ) пиримидина или их кислотно-аддитивных солей Download PDFInfo
- Publication number
- SU1022659A3 SU1022659A3 SU782700554A SU2700554A SU1022659A3 SU 1022659 A3 SU1022659 A3 SU 1022659A3 SU 782700554 A SU782700554 A SU 782700554A SU 2700554 A SU2700554 A SU 2700554A SU 1022659 A3 SU1022659 A3 SU 1022659A3
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- acid
- hydrogen
- pyrimidine
- oxo
- pyrido
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D213/79—Acids; Esters
-
- 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
- A61P25/04—Centrally acting analgesics, e.g. opioids
-
- 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]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/08—Antiallergic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Veterinary Medicine (AREA)
- General Chemical & Material Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Neurology (AREA)
- Pain & Pain Management (AREA)
- Biomedical Technology (AREA)
- Neurosurgery (AREA)
- Pulmonology (AREA)
- Vascular Medicine (AREA)
- Cardiology (AREA)
- Immunology (AREA)
- Diabetes (AREA)
- Urology & Nephrology (AREA)
- Hematology (AREA)
- Anesthesiology (AREA)
- Rheumatology (AREA)
- Heart & Thoracic Surgery (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Pyridine Compounds (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
HU77CI1796A HU180701B (en) | 1977-12-29 | 1977-12-29 | Process for preparing pyrido-/1,2-a/pyrimidines containing a carboxylic or ester group on the pirimidimering |
Publications (1)
Publication Number | Publication Date |
---|---|
SU1022659A3 true SU1022659A3 (ru) | 1983-06-07 |
Family
ID=10994685
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
SU782700554A SU1022659A3 (ru) | 1977-12-29 | 1978-12-25 | Способ получени производных пиридо (1,2- @ ) пиримидина или их кислотно-аддитивных солей |
Country Status (8)
Country | Link |
---|---|
JP (1) | JPS5498797A (xx) |
BE (1) | BE873195A (xx) |
CH (1) | CH642368A5 (xx) |
DE (1) | DE2853273A1 (xx) |
FR (1) | FR2413375A1 (xx) |
GB (1) | GB2011410B (xx) |
HU (1) | HU180701B (xx) |
SU (1) | SU1022659A3 (xx) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
IL59802A (en) | 1979-05-08 | 1983-07-31 | Erba Farmitalia | Substituted pyrido(1,2-a)pyrimidine carboxylic acid derivatives,their preparation and pharmaceutical compositions containing them |
CN101628913B (zh) * | 2008-07-18 | 2013-01-23 | 中国科学院广州生物医药与健康研究院 | 用作雌激素相关受体调节剂的化合物及其应用 |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
HU168014B (xx) * | 1973-03-30 | 1976-02-28 | ||
US3898224A (en) * | 1974-09-09 | 1975-08-05 | Squibb & Sons Inc | 1,6,7,8-Tetrahydro-4-oxo-4H-pyrido {8 1,2-A{9 pyrimidine-9-carboalkoxy compounds |
HU173438B (hu) * | 1975-11-27 | 1979-05-28 | Chinoin Gyogyszer Es Vegyeszet | Sposob poluchenija novykh proizvodnykh 4-okso-1,6,7,8-/tetragidro-4h-pirido/1,2/pirimidina s zaderzhivajuhhejj vozgoranie aktivnot'ju i protivosvertivajuhhem effektom |
HU174693B (hu) * | 1976-02-12 | 1980-03-28 | Chinoin Gyogyszer Es Vegyeszet | Sposob poluchenija kondensirovannykh proizvodnykh pirimidina |
HU178910B (en) * | 1977-08-19 | 1982-07-28 | Chinoin Gyogyszer Es Vegyeszet | Process for preparing 2,3-disubstituted-4-oxo-4h-pyrido/1,2-a/-pyrimidines |
-
1977
- 1977-12-29 HU HU77CI1796A patent/HU180701B/hu unknown
-
1978
- 1978-12-09 DE DE19782853273 patent/DE2853273A1/de not_active Ceased
- 1978-12-25 SU SU782700554A patent/SU1022659A3/ru active
- 1978-12-27 JP JP16453378A patent/JPS5498797A/ja active Pending
- 1978-12-27 FR FR7836463A patent/FR2413375A1/fr active Granted
- 1978-12-28 CH CH1323178A patent/CH642368A5/de not_active IP Right Cessation
- 1978-12-28 GB GB7850108A patent/GB2011410B/en not_active Expired
- 1978-12-29 BE BE192660A patent/BE873195A/xx not_active IP Right Cessation
Non-Patent Citations (1)
Title |
---|
) 1. Vale II. L. and Spitzmiller E.R.. Tetrahydro-and Octahydropyr ido * |
Also Published As
Publication number | Publication date |
---|---|
FR2413375B1 (xx) | 1983-08-05 |
CH642368A5 (de) | 1984-04-13 |
JPS5498797A (en) | 1979-08-03 |
FR2413375A1 (fr) | 1979-07-27 |
BE873195A (fr) | 1979-04-17 |
GB2011410B (en) | 1982-09-22 |
GB2011410A (en) | 1979-07-11 |
HU180701B (en) | 1983-04-29 |
DE2853273A1 (de) | 1979-07-12 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Althuis et al. | Development of ethyl 3, 4-dihydro-4-oxopyrimido [4, 5-b] quinoline-2-carboxylate, a new prototype with oral antiallergy activity | |
Cheng et al. | Potential Purine Antagonists VII. Synthesis of 6-Alkylpyrazolo-[3, 4-d] pyrimidines1, 2a | |
NO151287B (no) | Analogifremgangsmaate for fremstilling av terapeutisk aktive 9-hydrazono-6,7,8,9-tetrahydro-4h-pyrido(1,2-a)-pyrimidinderivater | |
SU969165A3 (ru) | Способ получени конденсированных пиримидинов или их солей,или их оптических изомеров | |
Ferrarini et al. | One step synthesis of pyrimido [1, 2‐a][1, 8] naphthyridinones, pyrido [1, 2‐a] pyrimidinones and 1, 8‐naphthyridinones. Antihypertensive agents. V | |
SU1022659A3 (ru) | Способ получени производных пиридо (1,2- @ ) пиримидина или их кислотно-аддитивных солей | |
Angier et al. | Synthesis of pteroylglutamic acid. III | |
Suzuki et al. | Synthesis of antimicrobial agents. IV. Synthesis and antimicrobial activities of imidazo [4, 5-b][1, 8] naphthyridine derivatives | |
SU1217259A3 (ru) | Способ получени замещенных пиридо(1,2- @ )пиримидинов или их солей | |
Kurihara et al. | Reaction of ethyl 3‐ethoxymethylene‐2, 4‐dioxovalerate and ethyl ethoxymethyleneoxaloacetate with 3‐aminopyrazole analogs. Synthesis and chemistry of 3, 6, 7‐trisubstituted pyrazolo [1, 5‐a] pyrimidine derivatives | |
JPH0585553B2 (xx) | ||
SU589917A3 (ru) | Способ получени производных пиримидина | |
Ratajczyk et al. | The cyclocondensation of 5‐amino‐1, 3‐dimethylpyrazole with ethyl acetoacetate. Synthesis of isomeric pyrazolopyridones | |
Podanyi et al. | Nitrogen bridgehead compounds. Part 63. Ring-chain tautomerism of [(alpha-N-hetaryl) aminomethylene] malononitriles | |
SU931108A3 (ru) | Способ получени гексагидробензопирано/3,2-с/ пиридинов | |
JPS6045199B2 (ja) | 新規なイミダゾベンゾオキサジン及びそれらを含む製薬組成物 | |
US3539568A (en) | Process for preparing dicarboximide derivatives | |
MIYASHITA et al. | Ring Transformation of Condensed Pyrimidines by Enamines and Ynamines. Formation of Condensed Pyridines and Condensed Diazocines | |
SU730308A3 (ru) | Способ получени производных имидазо (1,5-а) /1,4/- диазепина или их солей | |
Gueiffier et al. | Heterocyclic compounds with a bridgehead nitrogen atom. Synthesis in the imidazo [1, 2‐c] quinazoline series | |
Ahmed | A Convenient Synthesis for Some New Pyrido [4′, 3′: 4, 5] thieno [2, 3-d] pyrimidines and Related Fused 1, 2, 4-Triazolo and 1, 3, 4-Thiadiazolo-derivatives | |
Kurihara et al. | Synthesis and reactions of ethyl 3‐acetyl‐8‐cyano‐6, 7‐dimethylpyrrolo [1, 2‐a] pyrimidine‐4‐carboxylate and related compounds | |
Kim et al. | Ring closure reaction of 4‐(2‐hydroxyanilino)‐2‐phenyl‐5‐pyrimidinecarboxylic acid with acetic anhydride. Synthesis of pyrimido [5, 4‐c][1, 5] benzoxazepin‐5 (11H) ones | |
NO144019B (no) | Analogifremgangsmaate for fremstilling av terapeutisk aktive naftyridinderivater | |
Santilli et al. | Synthesis of thiopyrano [2, 3‐d] pyrimidines and thieno [2, 3‐d] pyrimidines |