PL448397A1 - N,N-diphenyl-2-aminosumane and method of obtaining it - Google Patents
N,N-diphenyl-2-aminosumane and method of obtaining itInfo
- Publication number
- PL448397A1 PL448397A1 PL448397A PL44839724A PL448397A1 PL 448397 A1 PL448397 A1 PL 448397A1 PL 448397 A PL448397 A PL 448397A PL 44839724 A PL44839724 A PL 44839724A PL 448397 A1 PL448397 A1 PL 448397A1
- Authority
- PL
- Poland
- Prior art keywords
- diphenyl
- aminosumane
- obtaining
- tricyclopenta
- jkl
- Prior art date
Links
- 238000000034 method Methods 0.000 title abstract 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 abstract 2
- -1 N,N-diphenyl-4,7-dihydro-1H-tricyclopenta[def,jkl,pqr]triphenylene-2-amine Chemical compound 0.000 abstract 2
- 239000011541 reaction mixture Substances 0.000 abstract 2
- 230000009897 systematic effect Effects 0.000 abstract 2
- 229910021595 Copper(I) iodide Inorganic materials 0.000 abstract 1
- 238000004440 column chromatography Methods 0.000 abstract 1
- LSXDOTMGLUJQCM-UHFFFAOYSA-M copper(i) iodide Chemical compound I[Cu] LSXDOTMGLUJQCM-UHFFFAOYSA-M 0.000 abstract 1
- 238000000605 extraction Methods 0.000 abstract 1
- 239000011261 inert gas Substances 0.000 abstract 1
- 239000003446 ligand Substances 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 239000003960 organic solvent Substances 0.000 abstract 1
- 239000002244 precipitate Substances 0.000 abstract 1
- 239000000047 product Substances 0.000 abstract 1
- 238000010992 reflux Methods 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C13/00—Cyclic hydrocarbons containing rings other than, or in addition to, six-membered aromatic rings
- C07C13/28—Polycyclic hydrocarbons or acyclic hydrocarbon derivatives thereof
- C07C13/32—Polycyclic hydrocarbons or acyclic hydrocarbon derivatives thereof with condensed rings
- C07C13/62—Polycyclic hydrocarbons or acyclic hydrocarbon derivatives thereof with condensed rings with more than three condensed rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C5/00—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms
- C07C5/42—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms by dehydrogenation with a hydrogen acceptor
- C07C5/50—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms by dehydrogenation with a hydrogen acceptor with an organic compound as an acceptor
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K11/00—Luminescent, e.g. electroluminescent, chemiluminescent materials
- C09K11/06—Luminescent, e.g. electroluminescent, chemiluminescent materials containing organic luminescent materials
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Przedmiotem wynalazku jest N,N-difenylo-2-aminosumanen o nazwie systematycznej N,N-difenylo-4,7-dihydro-1H-tricyklopenta[def,jkl,pqr]trifenyleno-2-amina o wzorze 1. Kolejnym przedmiotem wynalazku jest sposób otrzymywania N,N-difenylo-2-aminosumanenu o nazwie systematycznej N,N-difenylo-4,7-dihydro-1H-tricyklopenta[def,jkl,pqr]trifenyleno-2-amina o wzorze 1, charakteryzujący się tym, że przygotowuje się mieszaninę 2-halogenosumanenu, jodku miedzi(I), liganda oraz zasady w rozpuszczalniku organicznym w stosunku molowym 1:1:(0,2 do 2,0):2, następnie mieszaninę reakcyjną ogrzewa się przez 24 godziny w temperaturze wrzenia w atmosferze gazu obojętnego, po czym do mieszaniny dodaje się 1M roztwór kwasu solnego, a uzyskany osad wydziela się z mieszaniny reakcyjnej na drodze ekstrakcji, a czysty produkt wyodrębnia się na drodze chromatografii kolumnowej.The subject of the invention is N,N-diphenyl-2-aminosumane with the systematic name N,N-diphenyl-4,7-dihydro-1H-tricyclopenta[def,jkl,pqr]triphenylene-2-amine of the formula 1. Another subject of the invention is a method for obtaining N,N-diphenyl-2-aminosumane with the systematic name N,N-diphenyl-4,7-dihydro-1H-tricyclopenta[def,jkl,pqr]triphenylene-2-amine of the formula 1, characterized in that a mixture of 2-halogenosumane, copper(I) iodide, ligand and base in an organic solvent in a molar ratio of 1:1:(0.2 to 2.0):2 is prepared, then the reaction mixture is heated for 24 hours at reflux temperature in an inert gas atmosphere, after which a 1M solution of hydrochloric acid, the obtained precipitate is separated from the reaction mixture by extraction and the pure product is isolated by column chromatography.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| PL448397A PL448397A1 (en) | 2024-04-24 | 2024-04-24 | N,N-diphenyl-2-aminosumane and method of obtaining it |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| PL448397A PL448397A1 (en) | 2024-04-24 | 2024-04-24 | N,N-diphenyl-2-aminosumane and method of obtaining it |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| PL448397A1 true PL448397A1 (en) | 2024-10-21 |
Family
ID=93155075
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PL448397A PL448397A1 (en) | 2024-04-24 | 2024-04-24 | N,N-diphenyl-2-aminosumane and method of obtaining it |
Country Status (1)
| Country | Link |
|---|---|
| PL (1) | PL448397A1 (en) |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1604949A2 (en) * | 2003-01-31 | 2005-12-14 | Nippon Shokubai Co., Ltd. | Sumanene and process for production thereof |
-
2024
- 2024-04-24 PL PL448397A patent/PL448397A1/en unknown
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1604949A2 (en) * | 2003-01-31 | 2005-12-14 | Nippon Shokubai Co., Ltd. | Sumanene and process for production thereof |
Non-Patent Citations (2)
| Title |
|---|
| DOMINIKA UFNAL ET AL.: "Organic & Biomolecular Chemistry, issue 25, 2024, p.1-10 https://www.researchgate.net/publication/380609522_Sumanene-carbazole_conjugate_with_push-pull_structure_and_its_chemoreceptor_application", SUMANENE–CARBAZOLE CONJUGATE WITH PUSH–PULL STRUCTURE AND ITS CHEMORECEPTOR APPLICATION * |
| SHAKEEL ALVI AND RASHID ALI: "Beilstein J. Org. Chem. 2020, 16, 2212–2259, https://www.beilstein-journals.org/bjoc/content/pdf/1860-5397-16-186.pdf", SYNTHETIC APPROACHES TO BOWL-SHAPED Π-CONJUGATED SUMANENE AND ITS CONGENERS * |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| KR20070088485A (en) | Purification of cinacalcet | |
| SG192675A1 (en) | New iridium-based complexes for ecl | |
| PL448397A1 (en) | N,N-diphenyl-2-aminosumane and method of obtaining it | |
| Matveeva et al. | Efficient synthesis of racemic β-aminophosphonates via aza-Michael reaction in water | |
| Pankov et al. | Synthesis and a combined experimental/theoretical structural study of a comprehensive set of Pd/NHC complexes with o-, m-, and p-halogen-substituted aryl groups (X= F, Cl, Br, CF 3) | |
| Ghiazza et al. | Visible-light-mediated synthesis of trifluoromethylthiolated arenes | |
| CN103370330B (en) | New complex based on iridium for ECL | |
| JP6112659B2 (en) | Methods for producing sulfonyl azide derivatives and acylsulfonamide derivatives and their use. | |
| EP2272851B1 (en) | Fluorinated boronic acid ester compound and process for production thereof | |
| CN115103833A (en) | Production method of difluoromethyl substituted aromatic heterocyclic compound | |
| Alomari et al. | Design, synthesis and biological evaluation of potent thiazolidinedione salicylic acid inhibitors against glyoxalase-I as potential anticancer agents | |
| CN107163042B (en) | Preparation process of a novel fluorescent probe for the detection of hydrazine | |
| Shagun et al. | Tentative mechanisms of 1, 2-dihydropyridine and 4H-pyran formation via the reaction of 3-trimethylsilyl-2-propyn-1-al with 2-aminopyridine and water: experimental and quantum chemistry studies | |
| Wang et al. | A general and efficient route to 3-amino-4-sulfanylcoumarins via substitution and palladium-catalyzed amination of 3-bromo-4-tosyloxycoumarins | |
| Wu et al. | DBU‐Mediated [4+ 2] Cyclization of Sulfoxonium Ylides and o‐Phenylenediamines for Quinoxaline Synthesis | |
| Palacios et al. | Synthesis of novel 2, 5-dihydro-1, 5, 2-diazaphosphinines from primary enamine phosphonates and from alkyl phosphonates | |
| Zapol’skii et al. | Chemistry of Polyhalogenated Nitrobutadienes, 2: Synthesis of N-Tetrachloroallylidene-N′-arylhydrazines by a Formal Synproportionation Reaction | |
| US11478481B2 (en) | Process for preparation of optically pure and optionally substituted 2-(1-hydroxy-alkyl)-chromen-4-one derivatives and their use in preparing pharmaceuticals | |
| PL448582A1 (en) | Method for obtaining 1,1'-bis-(E)-(α,β-unsaturated) carbonyl derivatives of ferrocene | |
| RU2577543C1 (en) | METHOD FOR SYNTHESIS OF 4a,5b,10,12-TETRAAZAINDENO[2,1-b]FLUORENE | |
| JP2001213819A (en) | Method of production for cyclophane derivative | |
| US20220056054A1 (en) | Methods of preparation of aminoboranes and applications for borylation and suzuki coupling | |
| JP4389548B2 (en) | An inclusion compound of an arylamine derivative having a fluorene skeleton and an aromatic hydrocarbon, and a method for separating and purifying the arylamine derivative. | |
| Sielemann et al. | Star-shaped threefold dihydropyridine and xanthene derivatives | |
| JP2012184186A (en) | Method for producing pyrene derivative |