| abstract |
A COMPOUND OF FORMULA I FIGURE 1 CHARACTERIZED BECAUSE R1 and R2, INDEPENDENTLY, ARE HYDROGEN, ALKYL FROM 1 TO 4 ATOMS OF CARBON, ALCOXY FROM 1 TO 4 ATOMS OF CARBON, ALKYLTIUM FROM 1 TO 4 ATOMS OF CARBON, HALOGEN, TRIFLUOROMETHYL, TRIFLUOROMETO- XI, CIANO, ALCANOYL FROM 2 TO 5 ATOMS OF CARBON, ALKYL SULPHONYL FROM 1 TO 4 ATOMS OF CARBON OR SUL-FAMOIL, R3 IS HYDROXY, AXYL, AQUI TO 4 ATOMS OF CARBON, HALOGEN, CIANO, ALCANOYL FROM 2 TO 5 ATOMS OF CARBON, CARBAMOIL, ALKYL SULFONYLOXY FROM 1 TO 4 ATOMS OF CARBON, OR TRIFLUOROMETILSULFONILOXY, AND R4 and R5, INDEPENDENTE 1 TO 4 ATOMS OF CARBON, HYDROXYALKYL 2 TO 4 ATOMS OF CARBON, OR PHENYLALKYL 1 TO 4 ATOMS OF CARBON, OR FORMED WITH THE NITROGEN ATOMS TO WHICH THEY ARE UNITED, A GROUP PIRROLIL- DINILO, PIPERINO IN THE FORM OF A FREE BASE OR ACID ADDITION SALT. 5. A PROCESS CHARACTERIZED BECAUSE IT IS FOR THE PRODUCTION OF A 1, 2, 3, 4-TETRAHIDRO-2-NAFTALE-NAMINA THAT PRESENTS A PHENYL SUBSTITUTE IN THE AROMATIC RING, AND SALTS OF ADDITION OF ACID OF THE SAME, THEREFORE A 1, 2, 3, 4-TETRAHYDRO-2-NAFTALENAMINE PRESENTING A HALOGEN IN THE AROMATIC RING IS REACTIONED WITH OPTIONALLY REPLACED FENYL-BORONIC ACID AND THE RESULTING COMPOUND IS RECOVERED IN A FREE BASED OR IN THE FORM OF A ACID. . |