PL448397A1 - N,N-diphenyl-2-aminosumane and method of obtaining it - Google Patents

N,N-diphenyl-2-aminosumane and method of obtaining it

Info

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
Application number
PL448397A
Other languages
Polish (pl)
Inventor
Artur Kasprzak
Jakub Cyniak
Original Assignee
Politechnika Warszawska
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Politechnika Warszawska filed Critical Politechnika Warszawska
Priority to PL448397A priority Critical patent/PL448397A1/en
Publication of PL448397A1 publication Critical patent/PL448397A1/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C13/00Cyclic hydrocarbons containing rings other than, or in addition to, six-membered aromatic rings
    • C07C13/28Polycyclic hydrocarbons or acyclic hydrocarbon derivatives thereof
    • C07C13/32Polycyclic hydrocarbons or acyclic hydrocarbon derivatives thereof with condensed rings
    • C07C13/62Polycyclic hydrocarbons or acyclic hydrocarbon derivatives thereof with condensed rings with more than three condensed rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C5/00Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms
    • C07C5/42Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms by dehydrogenation with a hydrogen acceptor
    • C07C5/50Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms by dehydrogenation with a hydrogen acceptor with an organic compound as an acceptor
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K11/00Luminescent, e.g. electroluminescent, chemiluminescent materials
    • C09K11/06Luminescent, 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.

PL448397A 2024-04-24 2024-04-24 N,N-diphenyl-2-aminosumane and method of obtaining it PL448397A1 (en)

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)

* Cited by examiner, † Cited by third party
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

Patent Citations (1)

* Cited by examiner, † Cited by third party
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)

* Cited by examiner, † Cited by third party
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