首页> 外国专利> METHOD OF PRODUCING 2,9-BIS-SUBSTITUTED TRANS-2,3A,7B,9,10A,14B-HEXAAZAPERHYDRODIBENZOTETRACENES BASED ON AMINO DERIVATIVES OF METHYL ESTER OF MALEOPIMARIC ACID

METHOD OF PRODUCING 2,9-BIS-SUBSTITUTED TRANS-2,3A,7B,9,10A,14B-HEXAAZAPERHYDRODIBENZOTETRACENES BASED ON AMINO DERIVATIVES OF METHYL ESTER OF MALEOPIMARIC ACID

机译:基于马来酸甲基酯的氨基衍生物的2,9-BIS取代的TRANS-2,3A,7B,9,10A,14B-六氮杂双苯并戊二烯的制备方法

摘要

FIELD: chemistry.;SUBSTANCE: invention relates to a method of producing 2,9-bis-substituted trans-2,3a,7b,9,10a,14b-hexaazaperhydrodibenzotetracenes of general formula (1):; ,;which can be used as candidate compounds for preparing preparations with antineoplastic activity and antiproliferative action, as well as N-containing chiral ligands, bifunctional and catalytic systems for enantioselective transformations.;EFFECT: novel method of producing 2,9-bis-substituted trans-2,3a,7b,9,10a,14b-hexaazaperhydrodibenzotetracenes, which involves reacting an amino compound of maleopimaric acid methyl ester with formaldehyde and trans-tetraazaperhydrotetracene in presence of 5–15 wt% of zeolite catalyst H-Ymmm in molar ratio, the amine derivative MPAME : formaldehyde : trans-tetraazaperhydrotetracene = 2:4:1 in CH3OH medium at temperature of ~20 °C and atmospheric pressure for 2_5–3_5 h.;1 cl, 1 tbl, 2 ex;где - where
机译:发明领域本发明涉及制备通式(1)的2,9-双取代的反式-2,3a,7b,9,10a,14b-六氮杂氢二苯并四氢呋喃的方法: ;可以用作制备具有抗肿瘤活性和抗增殖作用的制剂的候选化合物,以及含N的手性配体,对映选择性转化的双功能和催化体系。效果:生产2,9-双取代的反式2,3a,7b,9,10a,14b-六氮杂过氢二苯并四氢呋喃的新方法比例为5–15 wt%的沸石催化剂H-Ymmm的情况下,马来酸甲酯与甲醛和反式四氮杂过氢并四苯并胺的氨基化合物,胺衍生物MPAME:甲醛:反式四氮杂过氢并四苯甲烷在CH中为2:4:1 3 OH介质在约20°C的温度和大气压下进行2_5–3_5 h。; 1 cl,1 tbl,2 ex;где-其中

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