SU628819A3 - Способ получени производных тетрагидротиено /3,2-с/пиридина - Google Patents
Способ получени производных тетрагидротиено /3,2-с/пиридинаInfo
- Publication number
- SU628819A3 SU628819A3 SU762366005A SU2366005A SU628819A3 SU 628819 A3 SU628819 A3 SU 628819A3 SU 762366005 A SU762366005 A SU 762366005A SU 2366005 A SU2366005 A SU 2366005A SU 628819 A3 SU628819 A3 SU 628819A3
- Authority
- SU
- USSR - Soviet Union
- Prior art keywords
- tetrahydrothienopyridine
- producing derivatives
- producing
- hydrogen
- compounds
- Prior art date
Links
- 238000000034 method Methods 0.000 title description 4
- WJFYLCXWEXZNHU-UHFFFAOYSA-N 2,3,3a,4-tetrahydrothieno[3,2-b]pyridine Chemical class N1C=CC=C2SCCC21 WJFYLCXWEXZNHU-UHFFFAOYSA-N 0.000 title 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 4
- OJYDKYKQCVPTFG-UHFFFAOYSA-N 2,3,3a,4-tetrahydrothieno[3,2-c]pyridine Chemical class C1N=CC=C2SCCC21 OJYDKYKQCVPTFG-UHFFFAOYSA-N 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- 239000001257 hydrogen Substances 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- 238000006683 Mannich reaction Methods 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 125000004202 aminomethyl group Chemical group [H]N([H])C([H])([H])* 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 150000001728 carbonyl compounds Chemical class 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- -1 nitro, cyanoacetamido Chemical group 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 230000000144 pharmacologic effect Effects 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000003756 stirring Methods 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
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmacology & Pharmacy (AREA)
- Engineering & Computer Science (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (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 |
|---|---|---|---|
| FR7521549A FR2317303A1 (fr) | 1975-07-09 | 1975-07-09 | Procede de preparation de derives de la tetrahydrothieno (3,2-c) et (2,3-c) pyridine |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| SU628819A3 true SU628819A3 (ru) | 1978-10-15 |
Family
ID=9157715
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SU762366005A SU628819A3 (ru) | 1975-07-09 | 1976-06-09 | Способ получени производных тетрагидротиено /3,2-с/пиридина |
Country Status (26)
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5665315A (en) * | 1979-11-02 | 1981-06-03 | Nec Corp | Magnetic recording and inspecting system |
| DE3736664A1 (de) * | 1987-10-29 | 1989-05-11 | Boehringer Ingelheim Kg | Tetrahydro-furo- und -thieno(2,3-c)pyridine, ihre verwendung als arzneimittel und verfahren zu ihrer herstellung |
| NZ233654A (en) * | 1989-05-18 | 1993-02-25 | Bristol Myers Squibb Co | 2-aminomethyl-5-aminophenol derivatives; hair dye compositions containing them |
-
1975
- 1975-07-09 FR FR7521549A patent/FR2317303A1/fr active Granted
-
1976
- 1976-03-31 LU LU74674A patent/LU74674A1/xx unknown
- 1976-04-01 CH CH404576A patent/CH609349A5/xx not_active IP Right Cessation
- 1976-04-21 GR GR50593A patent/GR59812B/el unknown
- 1976-04-23 YU YU1030/76A patent/YU40137B/xx unknown
- 1976-05-06 PT PT65072A patent/PT65072B/pt unknown
- 1976-05-19 NL NL7605362A patent/NL7605362A/xx not_active Application Discontinuation
- 1976-05-21 IE IE1079/76A patent/IE42821B1/en unknown
- 1976-05-24 IL IL49641A patent/IL49641A/xx unknown
- 1976-05-31 ES ES448404A patent/ES448404A1/es not_active Expired
- 1976-06-01 ZA ZA763219A patent/ZA763219B/xx unknown
- 1976-06-03 AR AR263501A patent/AR211019A1/es active
- 1976-06-09 SU SU762366005A patent/SU628819A3/ru active
- 1976-06-10 CA CA254,573A patent/CA1071634A/en not_active Expired
- 1976-06-16 MX MX000320U patent/MX3224E/es unknown
- 1976-07-01 DK DK297876AA patent/DK141333B/da not_active IP Right Cessation
- 1976-07-01 PH PH7618641A patent/PH12311A/en unknown
- 1976-07-05 AT AT489876A patent/AT348526B/de not_active IP Right Cessation
- 1976-07-06 BE BE168664A patent/BE843822A/xx not_active IP Right Cessation
- 1976-07-07 DE DE19762630474 patent/DE2630474A1/de active Pending
- 1976-07-07 DD DD193745A patent/DD125081A5/xx unknown
- 1976-07-07 SE SE7607762A patent/SE421699B/xx not_active IP Right Cessation
- 1976-07-08 PL PL1976191016A patent/PL100685B1/pl unknown
- 1976-07-08 JP JP51081441A patent/JPS5236691A/ja active Granted
- 1976-07-08 GB GB28511/76A patent/GB1544093A/en not_active Expired
- 1976-07-09 HU HU76PA00001255A patent/HU172280B/hu unknown
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| HU198909B (en) | Process for producing pyridine-dicarbocylic acid esters | |
| Tohda et al. | Nucleophilic reaction upon electron-deficient pyridone derivatives. X. One-pot synthesis of 3-nitropyridines by ring transformation of 1-methyl-3, 5-dinitro-2-pyridone with ketones or aldehydes in the presence of ammonia. | |
| Okamoto et al. | Reaction Mechanism in Aromatic Heterocyclic Compound. I. The Reactions of N-Alkoxypyridinium Derivarives | |
| SU628819A3 (ru) | Способ получени производных тетрагидротиено /3,2-с/пиридина | |
| Radtke et al. | A Scalable, One-Pot Synthesis of 1, 2, 3, 4, 5-Pentacarbomethoxycyclopentadiene | |
| JPS623154B2 (enrdf_load_stackoverflow) | ||
| SU513624A3 (ru) | Способ получени производных 2-пиперазинил-тиазола | |
| US2507473A (en) | Coumaran derivatives and process for preparing same | |
| Furdui et al. | Improved synthesis of cationic pyridinium-substituted indolizines | |
| Marchalín et al. | Synthesis and reactions of 5-acetyl-2-amino-3-cyano-4-(5-X-2-furyl)-6-methyl-4H-pyrans | |
| Stepanova et al. | Silica-assisted reactions of pyrroles with 1-acyl-2-bromoacetylenes | |
| NO743980L (enrdf_load_stackoverflow) | ||
| SU833971A1 (ru) | Способ получени 3-фенил-2-оксо- - КАРбОлиНОВ | |
| Moon | Synthesis and acylation of pyrrolinones | |
| Groß et al. | Spin trapping of alkoxyl radicals generated from 5-methyl and 5-aryl-3-alkoxy-4-methylthiazole-2 (3H)-thiones in photochemically induced and microwave-initiated reactions | |
| Sasaki et al. | Studies on Heteroaromaticity. XXI. 1, 3-Dipolar Cycloaddition of N-Phenyl-C-(6-uracilyl) nitrone | |
| Reynolds et al. | Polynuclear Heterocycles. VIII. N-(2-Arylamino-1, 4-dioxynaphthyl-3) pyridinium Salts | |
| US11661407B2 (en) | Process for the preparation of pyrylium salts | |
| Woods | Bisacylation of 4-Pyrones | |
| Nasakin et al. | Synthesis of substituted pyridines by reaction of tetracyanoethylated ketones with hydrochloric and hydrobromic acids | |
| US3265700A (en) | Process for the production of substituted lactams | |
| US2658068A (en) | 3-(cyanomethyl) thianaphthene-1,1-dioxide | |
| Klemm et al. | Chemistry of thienopyridines. XXVIII. Mass spectra of fourteen substituted thienopyridines and nmr spectra of four picrates | |
| US4431586A (en) | Monocyclic telluropyrones | |
| Gray et al. | The nitration of some substituted 4-methylphenols; X-Ray crystal structure of (z)-3-bromo-5-(bromonitromethylene) furan-2 (5h)-one |