Aza- and polyaza-naphthalenyl carboxamide derivatives including certain quinoline carboxamide and naphthyridine carboxamide derivatives are described.
The carboxamide derivative provided is one produced by either of the carboxamide derivative production processes.
The N-acyl 2-oxindole-1-carboxamide intermediate may be converted to the 2-oxindole-1-carboxamide without isolation.
Compounds of the invention include N-(3-(trifluoromethyl)phenyl )-2-methyl-1-(3-morpholinopropyl )-5-phenyl-1 H-pyrrole-3-carboxamide, as well as other 2-phenyl-pyrrole carboxamide derivates and indole carboxamide derivatives.
Preferably, the coolant is a cyclic carboxamide such as N- ethyl-p-menthane-3 -carboxamide.
The invention is directed to novel indazole carboxamide derivatives.
The invention is directed to novel indole carboxamide compounds.
The invention is directed to novel indole carboxamide derivatives.
Aza- and polyaza-naphthalenyl carboxamide derivatives including certain quinoline carboxamide and naphthyridine carboxamide derivatives are described.
The other process for producing a carboxamide derivative comprises reacting the carboxamide with any of monohaloalkylcarboxylic acids and salts thereof.
The invention is directed to novel indazole carboxamide derivatives.
By reacting the N-(1-hydroxyethyl)carboxamide compound with an alcohol in the presence of an acid catalyst, the N-(1-alkoxyethyl)carboxamide compound is obtained.
A process for the product of a 2,3-cis-dihydroxycycloalkane-1-carboxamide, comprises dihydroxylation of the corresponding cycloalkene-1-carboxamide.
The invention is directed to novel indole carboxamide derivatives.
The invention is directed to novel azaindole and azaindazole carboxamide derivatives.
Requêtes fréquentes français :1-200, -1k, -2k, -3k, -4k, -5k, -7k, -10k, -20k, -40k, -100k, -200k, -500k, -1000k,
Requêtes fréquentes anglais :1-200, -1k, -2k, -3k, -4k, -5k, -7k, -10k, -20k, -40k, -100k, -200k, -500k, -1000k,
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