1.2- Diamino-1 -methyl

When M is Mo or W, the substitution reaction follows a two-term rate expression and in addition there is some replacement of the dipyridyl or 1,2-diamino-2-methyl propane but not of o-phenanthroline. The proportion of bidentate replacement to CO replacement is practically independent of the concentration... [Pg.42]

For example, the Nitrate, C4H7N5 + HNO3 prisms, explodes on heating. Many other reactions props of the Diamino-methyl-s-triazine are found in the Refs listed... [Pg.34]

Dialkylamino-dimethyl- XIII/8, 283 Dialkyl-dialkylamino- XIII/8, 285 Dialkyl-organoseleno- XIII/8, 275 Dialkyl-organothio- XIII/8, 275 Diamino-methyl- XIII/8, 222 Dihalogen-ethenyl- XIII/8, 173 Diorgano-(2-hydroxy-alkyl)- XIII/8, 85... [Pg.13]

Lobaplatin [D-19466 1,2-diamino-methyl-cyclo-butane-platinum(II) lactate], showed no nephrotoxic side effects as determined by the measurement of blood urea (Voegeli et al. 1990). It was cytotoxic in vitro for tumour cells in concentrations comparable to or lower than cytotoxic concentrations of cisplatin. It had excellent anticancer activity in vivo against a number of murine experimental tumours, including a cisplatin-resistant P388 line. [Pg.748]

R. W. Oehmke and J. C. Bailar, Jr., Some Coordination Compounds of the 2,2-Diamino-methyl-1,3-Diamino-Propane Moiety, J. Inorg. Nucl. Chem. 27 [10] 2199 (1965). [Pg.348]

AIkyI-substituted pyridazine-3(2//)-thiones undergo reaction with methyl iodide at the sulfur atom. Methylation of 4,5-diaminopyridazine-3(2ff)-thione with excess methyl iodide produces 4,5-diamino-l-methyIthiopyridazinium iodide (81JOC2467). [Pg.18]

Pteridine, 2,4-diamino-6-methyl-acylation, 3, 295 hydrolysis, 3, 294 synthesis, 3, 311... [Pg.752]

Pteridin-7-one, 2,4-diamino-8-hydroxy-structure, 3, 282 Pteridin-7-one, 5,6-dihydro-oxidation, 3, 307 structure, 3, 279 Pteridin-7-one, 8-hydroxy-synthesis, 3, 319 Pteridin-7-one, 8-methyl-synthesis, 3, 297... [Pg.755]

Pyridazinium iodide, 4,5-diamino-1-methyl-3-(methylthio)-analysis, 3, 2... [Pg.782]

Pyrrole, 3,4-dialkyl-2-ethyl-5-methyl-benzoylation, 4, 220 Pyrrole, 1,2-diamino-reactions, 4, 300 Pyrrole, 2,5-diamino-tautomerism, 4, 200, 299 Pyrrole, 2,4-diaryl-nitration, 4, 210 Pyrrole, 2,5-diaryl-synthesis, 4, 343 Pyrrole, 3,4-diaryl-synthesis, 4, 343 Pyrrole, di-t-butyl-protonation, 4, 47 Pyrrole, 2,5-dichloro-synthesis, 4, 368... [Pg.815]

Thiophene, 2-(dialkylamino)-5-methyl-synthesis, 4, 871 Thiophene, 2,4-diamino-reactions, 4, 812 synthesis, 4, 924... [Pg.890]

The preparation of 3,5-diamino derivatives from 3,5-dithioxotria-zines or from 6-methyl-3,5-dimethylmercapto-l,2,4-triazine was also described. ... [Pg.232]

A series of 2-aryloxazolo[4,5-/i]quinoline-5-arylidines was prepared by the reaction of 5,7-diamino-8-hydroxyquinoline with aromatic or aliphatic aldehydes in the presence of a basic catalyst such as piperidine. On the other hand, 2-styryl-5-diacetylamino-oxazolo[4,5-/i]quinolines were prepared by interaction of 2-methyl-5-diacetylamino-oxazolo[4,5-/i]quinoline with aromatic aldehydes (77MI1, 82MI2) (Scheme 6). [Pg.195]

S-Methyl thiourea Chloroformic acid methyl ester 3,4-Diamino-diphenyl-thioether... [Pg.621]

Chemical Name N-(4-([(2,4-Diamino-6-pteridinyl)methyl] methylamino] -benzoyl] -L-glutamic acid... [Pg.984]

Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...