首页> 外国专利> METHOD OF PRODUCING 12-CYCLOALKYL-12,13,13B,13C-TETRAHYDRO-6H,11H,14H-4B,5A,10B,12,13A-PENTAAZADIBENZOA,HCYCLOHEPTA1,2,3,4-DEFFLUORENES

METHOD OF PRODUCING 12-CYCLOALKYL-12,13,13B,13C-TETRAHYDRO-6H,11H,14H-4B,5A,10B,12,13A-PENTAAZADIBENZOA,HCYCLOHEPTA1,2,3,4-DEFFLUORENES

机译:制备12-环烷基-12,13,13B,13C-四氢-6H,11H,14H-4B,5A,10B,12,13A-五氮杂苯并[A,H]环己基[1,2,3,4-DEF ]氟

摘要

FIELD: chemistry.;SUBSTANCE: invention relates to a method of producing 12-cycloalkyl-12,13,13b,13c-tetrahydro-6H,11H,14H-4b,5a,10b,12,13a-pentaazadibenzo[a,h]cyclohepta[1,2,3,4-def]fluorenes of general formula (1). Method comprises reacting corresponding alkylamines of RNH2 with a paraform in a medium of CH3OH at temperature of 60 °C for 1 hour with subsequent addition to obtained reaction mixture at 20 °C catalyst NiCl2⋅6H2O and 1,1',2,2',3,3',4,4'-octahydro-2,2'-benzo-quinazoline in DMSO medium in molar ratio of cycloalkylamine: paraform: octahydro-biquinazoline: NiCl2⋅6H2O = 3:3:1:(0.03–0.07) and further stirring at temperature of 20 °C and atmospheric pressure for 2.5–3.5 hours; ;EFFECT: obtained according to the method of the compound of formula (1) can have fungicidal and insecticidal activity, as well as anti-inflammatory, antibacterial and antineoplastic properties.;1 cl, 1 tbl, 2 ex
机译:技术领域本发明涉及一种生产12-环烷基-12,13,13b,13c-四氢-6H,11H,14H-4b,5a,10b,12,13a-五氮杂二苯并[a,h]的方法通式(1)的环庚[1,2,3,4-def]芴。该方法包括使RNH 2 的相应烷基胺与亚型在CH 3 OH的介质中于60℃下反应1小时,随后在20℃下添加至获得的反应混合物中。 °C催化剂NiCl 2 ⋅6H 2 O和1,1',2,2',3,3',4,4'-八氢-2,2' -苯并喹唑啉在DMSO介质中的环烷基胺摩尔比为:paraform:八氢联喹啉:NiCl 2 ⋅6H 2 O = 3:3:1:(0.03-0.07 )并在20°C的温度和大气压下进一步搅拌2.5-3.5小时; 效果:根据式(1)化合物的方法获得,可以具有杀真菌和杀虫活性,以及​​抗炎,抗菌和抗肿瘤特性。1 cl,1 tbl,2 ex

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