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PROCESS FOR THE PREPARATION OF FURO (3,4-c) PYRIDINE DERIVATIVES IN NON-RACEMIC FORM.

机译:非自由基形式的呋喃(3,4-c)吡啶衍生物的制备方法。

摘要

The invention relates to a method for the preparation in non-racemic form of furo (3,4-c) pyridine derivatives of formula, (see FIG. 1) in which R3, R'3, R4 and R6 represent various substituents, the method comprising the resolution of a racemic mixture of one of the compounds of formulas: (see fig 2.3) in which R3, R'3, R4 and R6 are as defined above and R7 represents an acyl group comprising of 1 at 18 carbon atoms, by subjecting the selected compound to the action of an esterase capable of hydrolyzing the (+) or (-) enantiomer of said as a compound, then separating the hydrolyzed compound and the non-hydrolysed compound. The invention also relates to the enantiomers or mixtures of enantiomers thus obtained and their pharmaceutically acceptable salts.
机译:本发明涉及一种制备非外消旋形式的式(3,4-c)的呋喃(3,4-c)吡啶衍生物的方法(见图1),其中R 3,R′3,R 4和R 6代表各种取代基。包括拆分式(1)的化合物之一的外消旋混合物的方法(见图2.3),其中R3,R'3,R4和R6如上定义,R7代表在18个碳原子上包含1个酰基的酰基,通过使所选化合物经受能够水解所述化合物的(+)或(-)对映异构体的酯酶的作用,然后分离水解的化合物和未水解的化合物。本发明还涉及由此获得的对映异构体或对映异构体的混合物及其药学上可接受的盐。

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