FIELD: chemistry.
SUBSTANCE: formula (I) is obtained from protected precursor compound of the formula (II) , where R is carboxy protective group. Method involves protection removal from COOR carboxylic group linked to heterocyclic ring in the formula (II), thus obtaining respective free acid. Protection removal is performed in the presence of an alkali forming pharmaceutically acceptable salt with the indicated free acid and, if necessary, is followed by hydration of pharmaceutically acceptable perindopril salt.
EFFECT: improved method of perindopril obtainment.
15 cl, 1 dwg, 1 tbl, 7 ex
Authors
Dates
2008-11-27—Published
2003-11-18—Filed