where A - hydrogen, -SC-=N-R21)-NR22R23, -SH, SR2; R3 - free or esterified carboxyl-group; R4 - unsubstituted of substituted phenyl, naphthyl, 5- or 6-membered heterocyclic ring containing heteroatom taken from N, S or O; R5 - free or esterified carboxyl-group; R2 - phenyl, alkenyl, alkynyl, carboxyl-group; R6 - C1-C6-alkyl, haloidalkyl, CHO, -CN; n = 1-4; R21,R22,R23 - hydrogen, C1-C4-alkyl, phenylalkyl, acyl. Reagent 1: compound of the formula (II) where R3-R6,R21,R22,R23 and n have values indicated above. Reagent 2: chiral acid HB*R23. Reaction conditions: synthesized isothiouronium diastereoisomeric salts were separated and converted to other isothiouronium salts using achiral acids. Synthesized compounds were used in medicine as antihypertensive agents. ???EFFECT: improved method of synthesis. 10 cl"/> METHOD OF SYNTHESIS OF PURE ENANTIOMERS OF 1,4-DIHYDROPYRIDINES, PURE ENANTIOMERS OF 1,4-DIHYDROPYRIDINES AND ISOTHIOUREIDES
首页> 外国专利> METHOD OF SYNTHESIS OF PURE ENANTIOMERS OF 1,4-DIHYDROPYRIDINES, PURE ENANTIOMERS OF 1,4-DIHYDROPYRIDINES AND ISOTHIOUREIDES

METHOD OF SYNTHESIS OF PURE ENANTIOMERS OF 1,4-DIHYDROPYRIDINES, PURE ENANTIOMERS OF 1,4-DIHYDROPYRIDINES AND ISOTHIOUREIDES

机译:1,4-二氢吡啶的纯对映体,1,4-二氢吡啶的纯对映体和异硫脲的合成方法

摘要

FIELD: organic chemistry. SUBSTANCE: products: pure enantiomers of 1,4-dihydropyridines of the formula (I) where A - hydrogen, -SC-=N-R21)-NR22R23, -SH, SR2; R3 - free or esterified carboxyl-group; R4 - unsubstituted of substituted phenyl, naphthyl, 5- or 6-membered heterocyclic ring containing heteroatom taken from N, S or O; R5 - free or esterified carboxyl-group; R2 - phenyl, alkenyl, alkynyl, carboxyl-group; R6 - C1-C6-alkyl, haloidalkyl, CHO, -CN; n = 1-4; R21,R22,R23 - hydrogen, C1-C4-alkyl, phenylalkyl, acyl. Reagent 1: compound of the formula (II) where R3-R6,R21,R22,R23 and n have values indicated above. Reagent 2: chiral acid HB*R23. Reaction conditions: synthesized isothiouronium diastereoisomeric salts were separated and converted to other isothiouronium salts using achiral acids. Synthesized compounds were used in medicine as antihypertensive agents. ???EFFECT: improved method of synthesis. 10 cl
机译:领域:有机化学。物质:产品:式(I)的1,4-二氢吡啶的纯对映体其中A-氢,-SC- = NR 21 )-NR 22 R 23 ,-SH,SR 2 ; R 3 -游离或酯化的羧基; R 4 -未取代的,取自N,S或O的取代的苯基,萘基,5元或6元杂环含杂原子; R 5 -游离或酯化的羧基; R 2 -苯基,烯基,炔基,羧基; R 6 -C 1 -C 6 -烷基,卤代烷基,CHO,-CN; n = 1-4; R 21 ,R 22 ,R 23 -氢,C 1 -C 4 其中R 3 -R 6 ,R 21 ,R 22 ,R 23 和n具有上述值。试剂2:手性酸HB * R 23 。反应条件:分离合成的异硫脲铀非对映异构体盐,并使用非手性酸将其转化为其他异硫脲铀盐。合成的化合物在医学上用作降压药。效果:改进的合成方法。 10厘升

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