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Synthesis of novel 3-(2-chloroquinolin-3-yl)-n-cyclohexylquinoxalin-2-amines and antibacterial activity thereof

机译:新型3-(2-氯喹啉-3-基)-正环己基喹喔啉-2-胺的合成及其抗菌活性

摘要

The present invention relates to a synthesis of novel 3-(2-chloroquinolin-3-yl)-N-cyclohexylquinoxalin-2-amines and antibacterial activity thereof. A process for producing a compound of the formula (JF) Wherein R1 represents a hydrogen atom, a nitro group, a chlorine atom or a methyl group, and R2 represents a hydrogen atom, a methyl group or.a methoxyl group. which comprises step 1 of reacting a compound of the formula (1) in the presence of acetic anhydride (Ac20), glacial acetic acid (AcOH) and sodium acetate (NaOAc) to obtain a compound of the formula (2); Wherein R2 has the same meaning as defined above, which comprises, step 2 of reacting the compound of formula (2) obtained in the step 1 and phosphoryl chloride (POCI3) in presence of N,N-dimethylformamide (DMF) to obtain the compound of the formula (3). Wherein R2 has the same meaning as defined above, Wherein R1 and R2 have the same meaning as defined above. and which comprises, step 3 of reacting the compound of formula (3) obtained in the step 2, compound of formula (4) and compound of formula (5) in presence of ethanol (EtOH) using ceric ammonium nitrate (CAN) as catalyst to obtain the compound of the formula (JF).
机译:本发明涉及新颖的3-(2-氯喹啉-3-基)-N-环己基喹喔啉-2-胺的合成及其抗菌活性。制备式(JF)化合物的方法,其中R1代表氢原子,硝基,氯原子或甲基,R2代表氢原子,甲基或甲氧基。所述方法包括步骤1:使式(1)的化合物在乙酸酐(Ac 2 O),冰醋酸(AcOH)和乙酸钠(NaOAc)的存在下反应以获得式(2)的化合物;其中R 2具有与上述定义相同的含义,其包括步骤2:在N,N-二甲基甲酰胺(DMF)的存在下,使步骤1中获得的式(2)的化合物与磷酰氯(POCl 3)反应。式(3)。其中R2具有与以上定义相同的含义,其中R1和R2具有与以上定义相同的含义。所述方法包括步骤3:使用硝酸铈铵(CAN)作为催化剂,在乙醇(EtOH)存在下,将步骤2中获得的式(3)化合物与式(5)化合物反应得到式(JF)的化合物。

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