[1]程德军,黄斌,李明田.N-烯丙基-N-(1-(5-溴-2-((4-氯苄基)氧基)苄基)-4-哌啶基)吡啶甲酰胺的合成及表征[J].江西师范大学学报(自然科学版),2014,(04):346-349.
 CHENG De-jun,HUANG Bin,LI Ming-tian.The Synthesis and Structural Characterization of N-Allyl-N-(1-(5-Brono-2-((4-Chlorobenzyl)Oxy)Benzyl)PiPeridin-4-Yl)Picolinanide[J].Journal of Jiangxi Normal University:Natural Science Edition,2014,(04):346-349.
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N-烯丙基-N-(1-(5-溴-2-((4-氯苄基)氧基)苄基)-4-哌啶基)吡啶甲酰胺的合成及表征()
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《江西师范大学学报》(自然科学版)[ISSN:1006-6977/CN:61-1281/TN]

卷:
期数:
2014年04期
页码:
346-349
栏目:
出版日期:
2014-08-31

文章信息/Info

Title:
The Synthesis and Structural Characterization of N-Allyl-N-(1-(5-Brono-2-((4-Chlorobenzyl)Oxy)Benzyl)PiPeridin-4-Yl)Picolinanide
作者:
程德军;黄斌;李明田
四川理工学院材料与化学工程学院,四川 自贡,643000
Author(s):
CHENG De-jun;HUANG Bin;LI Ming-tian
关键词:
HIV-1拮抗剂非肽类小分子化合物
Keywords:
HIV-1antagonistnon-peptide small molecular compounds
分类号:
O629
文献标志码:
A
摘要:
趋化因子受体 CCR5是 HIV-1病毒进入人体细胞的主要辅助受体,CCR5拮抗剂可作为一种靶向制剂,以防治人类 HIV-1感染。目前,非肽类小分子化合物 CCR5拮抗剂的研究占据主导地位。以4-氯苄氯、5-溴水杨醛为原料,通过消去、还原及溴化合成了4-溴-2-溴甲基-1-((4-溴苄基)氧)苯(中间体3),以哌啶-4-酮合成了 N-烯丙基-N-(4-哌啶基)吡啶甲酰胺(中间体7),通过中间体3和7合成了一种有望用作 CCR5拮抗剂的非肽类小分子化合物 N-烯丙基-N-(1-(5-溴-2-((4-氯苄基)氧基)苄基)-4-哌啶基)吡啶甲酰胺,该产物有一定的生物活性,并对该产物进行了1 H NMR、13 C NMR、IR 及 MS 表征。
Abstract:
Chemokine receptor CCR5 is a major coreceptor for HIV-1 entry into cell,CCR5 antagonists can be used as a targeting preparation in the prevention of human HIV-1 infection. At present,the peptide of small molecule compounds CCR5 antagonists research occupy the leading position. 4-bromo-2-(bromomethyl)-1-((4-chlorobenzyl) oxy)benzene( intermediate 3)was synthesized from 1-chloro-4-( chloromethyl)benzene and 5-bromo-2-hydroxy-benzaldehyde by elimination reaction,reduction reaction and bromization. N-allyl-N-( piperidin-4-yl)picolinamide (intermediate 7)was prepared from piperidin-4-one. Further reaction of intermediate 3 with intermediate 7 gave a novel non-peptide CCR5 antagonist N-allyl-N-(1-(5-bromo-2-((4-chlorobenzyl)oxy)benzyl)piperidin-4-yl)picoli-namide. The product has a certain biological activity,the compounds were characterized by 1 H NMR,13 C NMR,IR and MS.

参考文献/References:

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备注/Memo

备注/Memo:
国家自然科学基金(51303115)
更新日期/Last Update: 1900-01-01