Synthesis of 5-Substituted Hexahydro-1H-1, 4-Diazepine Analogues
O6; 5-Substituted hexahydro-1H-1,4-diazepine analogues were synthesized starting from N, N'-dibenzyl-1, 2-ethylenediamine and methyl 2, 4-dibromide butyrate through nucleophilic substitution, reduction, chlorination, debenzylation and amidation. Bioactivity tests showed that 9a had the highest agoni...
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Published in | 中国化学快报(英文版) Vol. 12; no. 11; pp. 951 - 954 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
Shanghai Institute of Materia Medica, Chinese Academy of Sciences,%Shanghai Jahwa Fine Chemicals Co. Ltd
01.11.2001
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Online Access | Get full text |
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Summary: | O6; 5-Substituted hexahydro-1H-1,4-diazepine analogues were synthesized starting from N,
N'-dibenzyl-1, 2-ethylenediamine and methyl 2, 4-dibromide butyrate through nucleophilic
substitution, reduction, chlorination, debenzylation and amidation. Bioactivity tests showed that 9a
had the highest agonist activity. |
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ISSN: | 1001-8417 1878-5964 |