Methylamine and derivs

Dipicryl-methylamine. See under Diphenyl-methylamine and Derivatives... 

Diphenyl-methylamine and derivs 5 D1468 2,4,6,2, 4,6,-hexanitrodiphenylmethylamine 5 D1468... 

Dimethylformamide, Methylamine and Derivatives Process Technologies, Davy Process Technology, www.davyprotech.com, 2003. 

METHYLAMINE AND DERIVATIVES Methylamine. This article supplements the one in Vol 1, A225—7 under Aminomethane and Derivatives CA Registry No 74-89-5 Uses in Explosives. Gaseous methylamine is passed into solid Amm Perchlorate below —6.3° to give useful monoproplnts. A mixt so prepd of 85% Amm Perchlorate and 15% methylamine has an Isp of 230 Ibsec/lb at 20atm (Ref 1). 

One-electron cleavage of the oxaziridine ring is especially useful in the case of the oxaziridine (114), easily obtained from cyclohexanone, methylamine and hypochlorite. The radical formed from (114) by uptake of one electron from the iron(II) ion can be trapped, for example, by acrylonitrile to form products derived from radical (297) (68TL5609). 

Blount and Robinson have extended this mode of synthesis to the preparation of iV-methyl/iomogranatonine (XXII) by the use of adipaldehyde, CHO. [CH2]4. CHO. The base, on reduetion with sodium in butyl aleohol, yields A -methyl/mmogranatoline (XXII CO — CHOH), the benzoyl derivative of which possesses marked local anaesthetic aetion. Similarly Blount, by eondensing /3-(o-formylphenyl)propaldehyde, CHO. CgH4. CHj. CHj. CHO, with methylamine and calcium acetonedicarboxylate, has prepared 8 9-benz-d - -feomogranatene-3-one (XXIII), which was reduced to the -alcohol (cf. reduction of tropinone to -tropine) and the latter converted to the benzoyl-derivative (m.p. 98°),... 

On the basis of the values of AS° derived in this way it appears that the chelate effect is usually due to more favourable entropy changes associated with ring formation. However, the objection can be made that and /3l-l as just defined have different dimensions and so are not directly comparable. It has been suggested that to surmount this objection concentrations should be expressed in the dimensionless unit mole fraction instead of the more usual mol dm. Since the concentration of pure water at 25°C is approximately 55.5 moldm , the value of concentration expressed in mole fractions = cone in moldm /55.5 Thus, while is thereby increased by the factor (55.5), /3l-l is increased by the factor (55.5) so that the derived values of AG° and AS° will be quite different. The effect of this change in units is shown in Table 19.1 for the Cd complexes of L = methylamine and L-L = ethylenediamine. It appears that the entropy advantage of the chelate, and with it the chelate effect itself, virtually disappears when mole fractions replace moldm . ... 

On boiling the methiodide with 70% sulfuric acid an N-methyl-oxo derivative was obtained, and this in turn gave 3-amino-2-phenyl-quinoline, methylamine, and ammonia on fusion with soda lime. The bulk of the evidence therefore favors quaternization at N-2 (cf, 154), in which case the acid-hydrolysis product is 155. Quaternization at N-2 would be expected because of the steric influence of the 10-phenyl group and the influence of the 4-amino group (cf. 4-hydroxy-pyridazine ) in the pyridazine-type ring, although the partial double-bond character of that ring is probably different from that in pyridazine itself. 

Formation of the partially saturated nitro derivatives 60 and 61 was reported by a Russian team <1994KGS1129>. The two products were obtained under fairly complicated reaction conditions when aminotetrazole 42 was first treated with potassium amidosulfonate and formaldehyde at pH = 4 followed by addition of nitric acid, methylamine, and acetic anhydride, product 60 was obtained in 24% yield. The same reaction, however, carried out at pH = 6 gave rise to formation of the acetoxy compound 61 in 21% yield. 

N-methylcarbamate and N,N -dimethylcarbamates have been determined in soil samples by hydrolyses with sodium bicarbonate and the resulting amines reacted with 4-chloro-7-nitrobenzo-2,l,3-Oxadiazole in isobutyl methyl ketone solution to produce fluorescent derivatives [81]. These derivatives were separated by thin layer chromatography on silica gel G or alumina with tetrahydrofuran-chloroform (1 49) as solvent. The fluorescence is then measured in situ (excitation at 436 nm, emission at 528 and 537nm for the derivatives of methylamine and dimethylamine respectively). The... 

Further transformation of the ester group in 126 was easily achieved. Thus, 126 with methylamine and 2-dimethylaminoethylamine gave the lactams 127 a and 127b. Reaction of the free acid derived from 126 with thionyl chloride yielded the lactone 127 c (Scheme 42) [7m, 60 a]. 

Piperidones of two types have been prepared from saccharide derivatives. Those of one type are lactams, exemplified by 187, obtained by oxidizing255 5-azido-5-deoxy-2,3-0-isopropyidene-/3-D-ribo-furanose (185) to 186, reducing the lactone 186 to the amine, and cyclizing this to 187. The other type comprises the 4-piperidones such as 189 this is obtained256 by oxidizing methyl a-D-arabinopyrano-side (188) with periodate, and treating the product with methylamine and 3-oxopentanedioic acid the bicyclic compound obtained from the a-glycoside differs from that from the /3 anomer. 

The only known derivatives of 1,4-dihydro-1,4-azaborine (16) are compounds (130). The ring was prepared from bis(4-methyl-2-lithiophenyl)methylamine and tri-n-butylborate. 

In the case of cationic complexes with unsaturated macrocycles two molecules of nucleophile, such as ammonia, amines and alkoxides, add to carbon atoms of two inline groups. For example, the reaction of [Ni(Bzo[16]octaeneN4)](C104)2 (Table 106) with sodium methoxide or ethoxide yields the compounds (395),2860 while with secondary amines and diamines complexes of type (396) are obtained.28 1 The reaction of (396) with acetone at room temperature yields complex (397) where the enolate anion of acetone, MeC(0)CH2, replaces the diethylamide group (Scheme 58). 2862 The addition of molecules such as bis(2-hydroxyethyl)methylamine and bis(2-hydroxyethyl) sulfide, HOCH2CH2YCH2CH2OH (Y = NMe, S) results in the formation of derivatives which possess one more coordination site just above the plane of the macrocyclic donors (398).2863... 

This is the only MMDA analogue that has been explored as an N-methyl derivative. A more highly substituted analogue has also been made, the N-methyl derivative of DMMDA. Isoapiole (see its preparation under DMMDA) was oxidized with formic acid and hydrogen peroxide to the ketone (2,5-dimethoxy-3,4-methylenedioxyphenylacetone, a solid with a mp of 75-76 °C from methanol) which was reductively aminated with methylamine and amalgamated aluminum to give 2,5-dimethoxy-N-methyl-3,4-methylenedioxyamphetamine hydrobromide... 

Anilinotoluen.es Phenyltoluidines Diphenyl-methylamines and Methyldiphenylamines, C H1SN. All isomers are described in Beil 12,180,787,857,905,(166) [ 105,436,467,4931 Anilinotoluene, Ar rfo-C13Hl2N4 and Diazido-C13HUN7 Derivatives were not found in Beil or CA through 1956... 

Jorgensen et al. developed the phenylalanine-derived catalyst 51 (Scheme 4.20), readily prepared in three high-yielding steps from L-phenylalanine, methylamine, and glyoxylic acid [34, 35]. 

Finally, the tetraacetate derivatives were synthesized from the bis(halogenomethyl) derivatives and iminobis(acetate) or from the bis(methylamines) and bromoacetate, and then were hydrolyzed to the target tetra(acetic acid) (scheme 9). 

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