Synthesis of Hexahydro-1H-1,4-diazepine analogues carrying the segment of (1-arylacetamide-2-tertiaryamide) ethane (II)
文献类型:期刊论文
作者 | Shen, JS![]() |
刊名 | ACTA CHIMICA SINICA
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出版日期 | 2001 |
卷号 | 59期号:8页码:1317-1322 |
关键词 | selective kappa receptor agonists hexahydro-1H-1,4-diazepine analogues (1-arylacetamide-2-tertiaryamide) ethane structure |
ISSN号 | 0567-7351 |
文献子类 | Article |
英文摘要 | 2-(1-(4-(N-phenyl-N- propionyl) amino) piperidyl)-hexahydro-1H-1,4-diazepine 7 was prepared starting from 3 through reduction, chlorination, amine substitution, and debenzylation. Seven target compounds of hexahydro-1H-1,4-diazepine analogues carrying the segment of (1- arylacetamide-2-tertiaryamide) ethane were synthesized through selective acylation and acylation of compound 7, and the four target compounds 10a similar to 10d containing hydrophilic group of hydroxy were achieved through debenzylation of 9a, 9b, 9c and 9d. These products were characterized by IR, EIMS, elementary analysis and H-1 NMR. Compounds of 9a similar to 9g and 10a similar to 10d were tested for their biological activities. |
WOS关键词 | RECEPTOR ; POTENT ; AGONISTS |
WOS研究方向 | Chemistry |
语种 | 中文 |
CSCD记录号 | CSCD:644199 |
WOS记录号 | WOS:000170513100027 |
出版者 | SCIENCE PRESS |
源URL | [http://119.78.100.183/handle/2S10ELR8/274530] ![]() |
专题 | 药物化学研究室 |
通讯作者 | Shen, JS |
作者单位 | Chinese Acad Sci, Shanghai Inst Mat Med, Shanghai 200031, Peoples R China |
推荐引用方式 GB/T 7714 | Shen, JS,Lei, LJ,Yan, TM,et al. Synthesis of Hexahydro-1H-1,4-diazepine analogues carrying the segment of (1-arylacetamide-2-tertiaryamide) ethane (II)[J]. ACTA CHIMICA SINICA,2001,59(8):1317-1322. |
APA | Shen, JS,Lei, LJ,Yan, TM,Wei, M,&Ji, RY.(2001).Synthesis of Hexahydro-1H-1,4-diazepine analogues carrying the segment of (1-arylacetamide-2-tertiaryamide) ethane (II).ACTA CHIMICA SINICA,59(8),1317-1322. |
MLA | Shen, JS,et al."Synthesis of Hexahydro-1H-1,4-diazepine analogues carrying the segment of (1-arylacetamide-2-tertiaryamide) ethane (II)".ACTA CHIMICA SINICA 59.8(2001):1317-1322. |
入库方式: OAI收割
来源:上海药物研究所
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