Abstract:
A PROCESS IS DISCLOSED FOR ALKYLATING PYRIDINE DERIVATIVES (INCLDING PYRIDINE) AND FOR OBTAINING ALKYL- AND CYCLOALKYL-DERIVATIVES OF PYRIDINE IN WHICH THE ALKYL OF CYCLOALKYL GROUP IS IN A 2, 4 OR 6 POSITION WITH RESPECT TO THE HETEROCYCLIC NIITROGEN ATOM, WHEREIN THE PYRIDINE DERIVATIVE IS REACTED IN AN AQUEOUS SOLUTION WITH A CARBOXYLIC ACID, R-COOH, WHEREIN R IS AN ALKYL OR A CYCLOALKYL GROUP HAVING FROM 1 TO 17 CARBON ATOMS, IN THE PRESENCE OF AN ALKALINE OR AMMONIUM PERSULPHATE AND OF CATALYTIC QUANTITIES OF AG+ IONS, AT ATMOSPHERIC PRESSURE AND AT TEMPERATURES BETWEEN 40* C. AND 100* C.
A PROCESS FOR ALKYLATING PYRIDINIC DERIVATIVES IS DISCLOSED, AND MORE PARTICULARLY THE ALKYLATION OF DERIVATIVES OF ISONICOTINIC ACID, IN ORDER TO OBTAIN 2-ALKYL DERIVATIVES HAVING THE FORMULA: WHEREIN R REPRESENTS AN ALKYL GROUP HAVING FROM 1 TO 4 CARBON ATOMS AND Y REPRESENTS A HYDROGEN ATOM OR A FUNCTIONAL GROUP COOR'' (WHEREIN R'' IS AN ALKYL GROUP HAVING FROM 1 TO 4 CARBON ATOMS), CONH2 OR CN, THE PROCESS BEING CHARACTERIZED IN THAT THE PYRIDINIC DERIVATIVE IS TREATED IN AN ACID AQUEOUS SOLUTION WITH A MIXTURE PREPARED SEPARATELY FROM A DIALKYLKETONE HAVING FROM 4 TO 6 CARBON ATOMS AND FROM HYDROGEN PEROXIDE, IN THE PRESENCE OF A FERROUS SALT, UNDER ATMOSPHERIC PRESSURE AND AT A TEMPERATURE BETWEEN 0* AND 50*C.
Abstract:
A PROCESS IS DISCLOSED FOR THE PREPARATION OF AMIDES OF NITROGEN AROMATIC HETEROCYCLIC BASES WHEREIN A HETEROAROMATIC BASE, PREFERABLY IN SALT FORM IS REACTED WITH A FORMAMIDE, HCONR2, WHEREIN R IS HYDROGEN OR AN ALKYL GROUP HAVING FROM 1 TO 5 CARBON ATOMS, PREFERABLY CH3, AND WITH A RADICAL R''O$ WHEREIN R'' IS HYDROGEN, AN ALKYL OR A CYCLOALKYL GROUP. THE SOURCE FOR THE R''O$ RADICALS IS A REDOX SYSTEM CONSISTING ESSENTIALLY OF R''OOH+FE++, WHEREIN R'' IS HYDROGEN, AN ALKYL OR A CYCLOALKYL GROUP, AT TEMPERATURES BETWEEN -10* AND 60*C., AND PREFERABLY AT TEMPERATURE BETWEEN -5* AND +35*C.