108-74-7Relevant articles and documents
N-LITHIUM DERIVATIVES OF ALIPHATIC AMINES IN THE SYNTHESIS OF 1-ALKYL-2-PHENYLDIAZENE 2-OXIDES
Shepelev, E. V.,Kostikova, N. N.,Dzhetigenov, B. A.,Kalinin, A. V.
, p. 1291 - 1293 (1991)
Magnesium derivatives of aliphatic amines containing α-hydrogen atoms, in contrast to t-BuNHMgBr, do not form phenylaliphatic diazene oxides upon reaction with nitrobenzene, but rather reduce it to azobenzene and azoxybenzene.Asymmetric diazene oxides are formed when the magnesium derivatives are replaced by lithium derivatives.The reaction of t-BuNHLi with dimethylnitramine gives 1,3,5-trimethyl-1,3,5-triazacyclohexane.
ELECTRONIC STRUCTURES AND THERMOLYSES OF 2-TETRAZENES
Heymanns, Peter,Rademacher, Paul
, p. 2511 - 2518 (1986)
The electronic structures and gas phase termolyses of the cyclic 2-tetrazenes 2 and 3 of open chain 1,1,4,4-tetramethyl-2-tetrazene (1) have been studied by photoelectron spectroscopy.While the six-membered ring compound 2 yields 1-methylmethylenamine (6) and nitrogen as fragments, the seven-membered ring compound 3 is contracted to 1,2-dimethylpyrazolidine (11).The acyclic 2-tetrazene 1 prefers disproportionation to 6 and dimethylamine (7).Based on MNDO calculations the ionization potentials of 1 - 3 were assigned to molecular orbitals.Several conformations of 2 and 3 were calculated.Compound 2 shows a rigid boat conformation with equatorial methyl groups, while 3 can occupy several conformations of similar energies.The different thermal decompositions of 1 - 3 are explained.
Flash Vacuum Thermolysis of α-Aminonitriles and Subsequent HCN Removal on Solid Base, a 'One Line' Multistep Sequence to Reactive N-Methyleneamines
Guillemin, J. C.,Denis, J. M.
, p. 951 - 952 (1985)
Reactive methyleneamines bearing alkyl or functional groups are isolated at low temperature in the condensate state by flash vacuum thermolysis of α-aminonitriles and subsequent vapour phase HCN removal on solid base.
Alkylation of 6-mercaptopurine (6-MP) with N-alkyl-N-alkoxycarbonylaminomethyl chlorides: S6-(N-alkyl-N-alkoxycarbonyl)aminomethyl-6-MP prodrug structure effect on the dermal delivery of 6-MP
Siver,Sloan
, p. 66 - 73 (1990)
The S6-(N-alkyl-N-alkoxycarbonyl)aminomethyl-6-MP (6-CARB-6-MP) prodrugs 5-20 were synthesized from the reaction of 6-MP weith N-alkyl-N-alkyoxycarbonylaminomethyl chlorides (4) in dimethyl sulfoxide in overall yields of 5-62%, depending on the N-alkyl and the alkoxy groups involved. The derivatives were fully characterized by spectral and micranalyses. The assignment of the substitution pattern as S6-alkyl was based on comparisons of the UV, 1H NMR and 13C NMR spectra with model compounds. A S6,9-bis-alkyl derivative was obtained from the reaction of 2 equivalents of 4 with 6-MP but the product was unstable and decomposed on standing to a 9-alkyl derivative. The 6-CARB-6-MP prodrugs reverted to 6-MP in water by an S(N)1-type mechanism involving unimolecular charge separation in the transition state of the rate determining step. There was no effect of dermal enzymes on the rate of hydrolysis. The solubilities in isopropyl myristate (IPM) for all of the 6-CARB-6-MP prodrugs were significantly greater than the solubility of 6-MP in IPM but only one prodrug (5) was apparently even as soluble as 6-MP in water. Selected 6-CARB-6-MP prodrugs were examined in diffusion cell experiments. Only the N-methyl-N-methoxycarbonyl derivative 5 gave a steady-state rate of delivery of 6-MP from IPM that was significantly greater than the steady-state rate of delivery of 6-MP from 6-MP in IPM. All the other derivatives gave steady-state rates of delivery of 6-MP from IPM that were either not significantly different, or were significantly lower than the rate obtained from 6-MP in IPM. In all cases, the effect of the 6-CARB-6-MP:IPM suspensions on the permeability of the skin, as determined by the second application flux of theophylline:propylene glycol, was of the same magnitude as the effect of IPM alone.
One-step synthesis of substituted 3,5-dinitropiperidines and 1,5-dinitro-3,7-diazabicyclo[3.3.1]nonanes from 1,3-dinitropropanes
Yarmukhamedov,Baibulatova,Dokichev,Khakimova,Spirikhin,Tomilov,Yunusov
, p. 414 - 420 (2005)
1,5-Dinitro-3,7-diazabicyclo[3.3.1]nonane derivatives were synthesized in up to 83%yields by the Mannich reaction of 1,3-dinitropropanes with excess formaldehyde and primary amines. In some cases, for instance, when 2,2-dimethyl-1,3-dinitropropane and benzylamine or monoethanolamine are used, the reaction occurs with low yields or stops at the step of formation of 3,5-dinitropiperidines. The influence of the structure of the starting compounds and reaction conditions on the yields of 1,5-dinitro-3,7-diazabicyclo[3.3.1] nonanes and 3,5-dinitropiperidines was studied.
Multiple N-H and C-H Hydrogen Atom Abstractions through Coordination-Induced Bond Weakening at Fe-Amine Complexes
Wang, Zongheng,Johnson, Samantha I.,Wu, Guang,Ménard, Gabriel
, p. 8242 - 8251 (2021/06/25)
We report the use of the reported Fe-phthalocyanine complex, PcFe (1; Pc = 1,4,8,11,15,18,22,25-octaethoxy-phthalocyanine), to generate PcFe-amine complexes 1-(NH3)2, 1-(MeNH2)2, and 1-(Me2NH)2. Treatment of 1 or 1-(NH3)2 to an excess of the stable aryloxide radical, 2,4,6-tritert-butylphenoxyl radical (tBuArO?), under NH3 resulted in catalytic H atom abstraction (HAA) and C-N coupling to generate the product 4-amino-2,4,6-tritert-butylcyclohexa-2,5-dien-1-one (2) and tBuArOH. Exposing 1-(NH3)2 to an excess of the trityl (CPh3) variant, 2,6-di-tert-butyl-4-tritylphenoxyl radical (TrArO?), under NH3 did not lead to catalytic ammonia oxidation as previously reported in a related Ru-porphyrin complex. However, pronounced coordination-induced bond weakening of both α N-H and β C-H in the alkylamine congeners, 1-(MeNH2)2 and 1-(Me2NH)2, led to multiple HAA events yielding the unsaturated cyanide complex, 1-(MeNH2)(CN), and imine complex, 1-(MeN═CH2)2, respectively. Subsequent C-N bond formation was also observed in the latter upon addition of a coordinating ligand. Detailed computational studies support an alternating mechanism involving sequential N-H and C-H HAA to generate these unsaturated products.
Synthesis of N-substituted 1,3,5-triazacyclohexanes catalyzed by starch sulfuric acid
Wu, Hui,Yuan, Rui,Wan, Yu,Yin, Wei,Pang, Li-Ling
experimental part, p. 1097 - 1102 (2012/03/11)
N-substituted 1,3,5-triazacyclohexanes were simply synthesized from the reaction of aromatic or fatty amines and formaldehyde catalyzed by recyclable starch sulfuric acid with good yields at room temperature.
Method of preparing electron deficient olefins
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Page/Page column 6, (2010/06/11)
This invention relates to a process for producing electron deficient olefins, such as 2-cyanoacrylates, using an iminium salt.
Benzo[b]thiophen-3(2H)-one 1,1-dioxide-a versatile reagent in the synthesis of spiroheterocycles
Cekavicus, Brigita,Vigante, Brigita,Liepinsh, Edvards,Vilskersts, Reinis,Sobolev, Arkadij,Belyakov, Sergey,Plotniece, Aiva,Mekss, Kristaps,Duburs, Gunars
experimental part, p. 9947 - 9952 (2009/04/03)
New applications of benzo[b]thiophen-3(2H)-one 1,1-dioxide have been investigated. The synthesis of a new heterocyclic system 3H,2′H-spiro[benzo[b]thieno[3,2-b]pyridine-3,2′-benzo[b]thiophene] is described and a mechanism for the cyclisation is proposed.
Ammonia-dimethylchloramine system: Kinetic approach in an aqueous medium and comparison with the mechanism involving liquid ammonia
Stephan,Pasquet,Elkhatib,Goutelle,Delalu
, p. 340 - 351 (2008/09/21)
After an exhaustive study of the system ammonia-dimethylchloramine in liquid ammonia, it was interesting to compare the reactivity of this system in liquid ammonia with the same system in an aqueous medium. Dimethylchloramine prepared in a pure state undergoes dehydrohalogenation in an alkaline medium: the principal products formed are N-methylmethanimine, 1,3,5- trimethylhexahydrotriazine, formaldehyde, and methylamine. The kinetics of this reaction was studied by UV, GC, and HPLC as a function of temperature, initial concentrations of sodium hydroxide, and chlorinated derivative. The reaction is of the second order and obeys an E2 mechanism (k1 =4.2 × 10-5 M-1 s-1, ΔH# = 82 kJ mol-1, ΔS# = -59 J mol-1 K-1) The oxidation of unsymmetrical dimethylhydrazine by dimethylchloramine involves two consecutive processes. The first step follows a first-order law with respect to haloamine and hydrazine, leading to the formation of an aminonitrene intermediate (k2 = 150 × 10-5 M-1 s -1). The second step corresponds to the conversion of aminonitrene into formaldehyde dimethylhydrazone at pH 13). This reaction follows a first-order law (k3 = 23.5 × 10-5 s-1) The dimethylchloramine-ammonia interaction corresponds to a SN2 bimoiecular mechanism (k4 = 0.9 × 10-5 M-1 s -1, pH 13, and T =25°C). The kinetic model formulated on the basis of the above reactions shows that the formation of the hydrazine in an aqueous medium comes under strong competition from the dehydrohalogenation of dimethylchloramine and the oxidation of the hydrazine formed by the original chlorinated derivative. A global model that explains the mechanisms both in an anhydrous and in an aqueous medium was elaborated.
