Towards molecular diversity: dealkylation of tert-butyl amine in Ugi-type multicomponent reaction product establishes tert-butyl isocyanide as a useful convertible isonitrile

2010 ◽  
Vol 8 (16) ◽  
pp. 3631 ◽  
Author(s):  
Sankar K. Guchhait ◽  
Chetna Madaan
1995 ◽  
Vol 34 (13) ◽  
pp. 3553-3554 ◽  
Author(s):  
Michael Buchmeiser ◽  
Richard R. Schrock

1996 ◽  
Vol 74 (4) ◽  
pp. 508-515 ◽  
Author(s):  
Svetlana V. Kudrevich ◽  
Johan E. Van Lier ◽  
Maria G. Galpern ◽  
Evgeny A. Luk'yanets

Several derivatives of 2,3-dicyanopyrazine were prepared via the condensation of o-quinones with diaminomaleodinitrile. Benzo[f]quinoxaline-2,3-dinitrile was obtained from 1,2-naphthoquinone, and a series of isomeric, di-tert-butyl substituted 5,6-(9,10-phenanthro)-2,3-dicyanopyrazines were prepared from the corresponding di-tert-butyl-9,10-phenanthrenequinones. Complexation of benzo[f]quinoxaline-2,3-dinitrile, and unsubstituted 5,6-(9,10-phenanthro)-2,3-dicyanopyrazine, with an appropriate metal salt yielded metal complexes of tetra-2,3-(benzo[f]quinoxalino)porphyrazine and tetra-2,3-[5,6-(9,10-phenanthro)]porphyrazine, respectively. Metal-free tetra-2,3-[5,6-(9,10-phenanthro)porphyrazine was obtained from the dilithium derivative by demetallation in HCl. These compounds have limited solubility in organic solvents, such as quinoline, and are aggregated in solutions. To eliminate the aggregation phenomenon and to determine the spectral properties of angularly annelated naphthalocyanine aza analogs, we prepared several isomeric tetra-2,3-[5,6-(di-tert-butyl-9,10-phenanthro)pyrazino]porphyrazines. These octa(tert-butyl) substituted complexes were synthesized via complexation of di-tert-butyl substituted 5,6-(9,10-phenanthro)-2,3-dicyanopyrazines with metal salts in the presence of urea, quinoline, and tri(n-butyl)amine, and purified by silica gel chromatography. They are soluble in chloroform and substantially monomerized in solutions. A hypsochromic shift of the Q-band of octaaza naphthalocyanines versus their carbocyclic analogs was observed for all aza analogs, with the extent of the shift depending on the composition of the aromatic macrocycle. Thus, the first angularly annelated benzo ring addition causes a hypsochromic shift (∼25 nm) of the Q-band of tetra-2,3-quinoxalinoporphyrazine, whereas addition of a second condensed benzo ring has little effect. Key words: phthalocyanine, aza analog, tetra-2,3-quinoxalinoporphyrazine, angular annelation.


2009 ◽  
Vol 10 (3) ◽  
pp. 356-361 ◽  
Author(s):  
Cecilia Sanna ◽  
Armida Sodo ◽  
Giuseppe Laguzzi ◽  
Giovanna Mancini ◽  
Marina Bicchieri

1963 ◽  
Vol 41 (1) ◽  
pp. 134-138 ◽  
Author(s):  
D. C. Bradley ◽  
E. G. Torrible

The aminolysis reactions involving primary amines with either Ti(NMe2)4 or Ti(NEt2)4 have been studied. The primary amines behave as bifunctional reactants, forming colored, insoluble, non-volatile bis-(primary amino)-titanium compounds Ti(NR)2 which (except for R = C6H5) are highly reactive towards water or alcohols. With n-butylamine, some soluble polymers of the general formula Tix(NBun)2x−2(NEt2)4 were isolated. With tert-butyl-amine the dimers Ti2(NBut)2(NMe2)4 and Ti2(NBut)2(NHBut)2(NMe2)2 were obtained. The structures of these polymeric metal–nitrogen compounds are discussed.


2019 ◽  
Vol 15 ◽  
pp. 2447-2457
Author(s):  
Gerardo M Ojeda ◽  
Prabhat Ranjan ◽  
Pavel Fedoseev ◽  
Lisandra Amable ◽  
Upendra K Sharma ◽  
...  

An efficient sequence based on the Ugi-azide reaction and rhodium(III)-catalyzed intermolecular annulation has been established for the preparation of tetrazole-isoquinolone/pyridone hybrids. Several N-acylaminomethyltetrazoles were reacted with arylacetylenes to form the hybrid products in moderate to very good yields. The method relies on the capacity of the rhodium catalyst to promote C(sp2)–H activation in the presence of a suitable directing group. The Ugi-azide reaction provides broad molecular diversity and enables the introduction of the tetrazole moiety, which may further assist the catalytic reaction by coordinating the metal center. The scope of the isoquinolones is very wide and may be extended to the preparation of complex compounds having heterocyclic moieties such as pyridone, furan, thiophene and pyrrole, as well as the corresponding benzo-fused derivatives. The developed procedure is simple, reproducible and does not require inert conditions.


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