Aminomethylation structure

Aldehyde 198 served as a key intermediate in a synthesis of the alkaloid ajmaline. The. Mannich aminomethylation transform triggers disconnection of two bonds in 198 to form dialdehyde 199, which by connective transform application can be converted to cyclopentene 200.58,59 The reduction in functional group reactivity and in structural complexity are both apparent by comparison of 198 and 200. 

Chemical Name a -(aminomethyl)-4-hvdroxybenzene-methanol hydrochloride Common Name Norsympatol hydrochloride norsynephrine hydrochloride Structural Formula hochcHjKHj... 

Ethane, (K)-l-cyclohexyl-L2-bis(diphenylphosphino)-rhodium complexes asymmetric hydrogenation, 6,253 Ethane, tetracyano-metal complexes, 2,263 Ethane, tetrakis(aminomethyl)-metal complexes, 2, 56 Ethane, tris[l, 1, l-(trisaminomethyl)]-complexes structure, 1,26... 

The Mannich condensation has traditionally been carried out in the presence of water as a three-component condensation involving a carbonyl compound (or related carbon nucleophile), formaldehyde, and a primary or secondary amine. The initial step is a condensation between the latter two reactants to form a mono- or dialkyl(methylene)ammonium ion which subsequently serves as the electrophilic partner in the reaction. With unsymmetrical ketones aminomethylation generally occurs at both positions to give mixtures of isomeric 3-amino ketones. The ratio of the isomers depends strongly on the structure of the ketone, and the more highly branched (3-amino ketone usually predominates. 

Molecular structure of a self-immolative AB6 dendron with aminomethyl-pyrene reporter units and a Boc protecting group as a trigger. 

Bulk electrochemical reduction of the platinum(IV) complex of the tridentate ligand l,l,l-tris(aminomethyl)ethane(tame), [Pt(tame)2]4+, leads to the quantitative formation of [Pt(tame)2]2+ (28), in which one of the amine donor groups in tame remains noncoordinated.141 The X-ray structure of the diprotonated complex [Pt(Htame)2]4+, as its tetrachlorozincate(II) salt, is also reported. 

A tetradentate ligand 2- bis[2-(2-pyridyl)ethyl]aminomethyl phenolate complexes zinc with an N30 donor set including pyridyl and phenolic groups. The X-ray structure reveals that a dimeric... 

However, compound 57, containing two 1,3-azaphosphetidine fragments, obtained by heating tetrakis(aminomethyl)phosphonium (38) chloride or tris(anilinomethyl)phosphine (40) in ethanol, is described in Eq. (28) (72JOC2752 77JOC4040). A detailed analysis of NMR spectra made it possible to reject a structure with two five-membered rings. 

N-[3-(aminomethyl)benzyl]acetamidine (1400W) Fig 10 8 structure of 1400W. 

NAD-malic enzyme, 52t, 62-63 A,A-dimethyl-2-(aminomethyl)phenyl benzylselenoxide, 103 A,A-dimethyl-2-(aminomethyl)phenyl bromotelluronium iodide, 91 A,A-dimethyl-2-(aminomethyl)phenyl iodotelluronium iodide, 91 A,A-dimethyl-2-(aminomethyl)phenyl phenyltelluride, 110 Non-covalent molecular structures... 

For the synthesis of perfectly dendronized sohd-phase polymers (Fig. 7.4) various dendritic structures were prepared based on amide connections [6]. For example, the naturally occurring amino acid lysine was used as a building block in creating a dendritic scaffold [33]. The synthesis of symmetrical tri-branching den-drimers on aminomethyl polystyrene macrobeads was also described in literature [34]. Recently, aryl ether dendrimers were prepared on hydroxymethyl polystyrene using a Mitsunobu reaction with 3,5-bis(acetoxymethyl)phenol [35]. 

Nizatidine Nizatidine is N-[2-[[[2-[(dimethylamino)methyl]-4-thiazolyl]methyl] thio] ethyl]-2-nitro-l,l-ethenediamine (16.2.15). According to its chemical structure, nizatidine is somewhat of a hybrid structure of ranitidine and famotidine, in which a side chain of ranitidine and carrying heterocycle, 2-aminothiazol, are used. Likewise, its synthesis also is a specific combination of pathways used for making both prototype drugs. 2-(Dimethyl-aminomethyl)-4-hydroxymethylthiazol serves as the initial compound, from which the desired nizatidine (16.2.15) is synthesized by subsequent reaction with 2-mercaptoethy-lamine hydrochloride and then with iV-methyl-l-methythio-2-nitroethenamine [71,72]. 

Later, Tieke reported the UV- and y-irradiation polymerization of butadiene derivatives crystallized in perovskite-type layer structures [21,22]. He reported the solid-state polymerization of butadienes containing aminomethyl groups as pendant substituents that form layered perovskite halide salts to yield erythro-diisotactic 1,4-trans polymers. Interestingly, Tieke and his coworker determined the crystal structure of the polymerized compounds of some derivatives by X-ray diffraction [23,24]. From comparative X-ray studies of monomeric and polymeric crystals, a contraction of the lattice constant parallel to the polymer chain direction by approximately 8% is evident. Both the carboxylic acid and aminomethyl substituent groups are in an isotactic arrangement, resulting in diisotactic polymer chains. He also referred to the y-radiation polymerization of molecular crystals of the sorbic acid derivatives with a long alkyl chain as the N-substituent [25]. More recently, Schlitter and Beck reported the solid-state polymerization of lithium sorbate [26]. However, the details of topochemical polymerization of 1,3-diene monomers were not revealed until very recently. 

Figure 7.66. Proposed structure of 797 derived from metalation of 2-(aminomethyl)-5(4//)-oxazolones.

The alkylzinc amide compounds 210 , 211 ° and 212 derived from the corresponding 2-(aminomethyl)pyridines, have structural features identical to those of 203-208 (Figure 100). They form dimers in which the amide nitrogen atom is /z -bridged between... 

Dossing, A. Toftlund, H. Hazell, A. Bourassa, J. Ford, P. C. Crystal structure, luminescence and other properties of some lanthanide complexes of the polypyridine ligand 6,6,-bis[bis(2-pyridylmethyl)aminomethyl]-2,2,-bipyridine. J. Chem. Soc., Dalton Trans. 1997, (3), 335-339. 

Most possibilities and most examples in the syntheses of 1,4-dihydro-3(2//)-isoquinolinone (2) and its derivatives involve the cyclization of the corresponding arylacetic acid derivatives. The opportunity arises from the lactam structure of compound 2. With suitable reagents, different o-aminomethyl-, o-hydroxymethyl-, or o-chloromethyl-phenylacetic acid derivatives (25LA225 66JPR12 69CJC864 84JHC297) and o-hydroxymethyl phenylacetonitriles (85S114) can be cyclized. 

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