Journal of Heterocyclic Chemistry p. 1107 - 1109 (1983)
Update date:2022-08-04
Topics: Elemental analysis Functionalization Nuclear magnetic resonance (NMR) spectroscopy Infrared (IR) spectroscopy Mass spectrometry (MS) TLC (thin-layer chromatography) X-ray crystallography Purification Starting Material Reaction Conditions UV-Vis Spectroscopy Melting Point/Boiling Point
Gill
Bracher
2,7-Diazaphenanthrene was synthesised in moderate yield by the modified Pomeranz-Fritsch reaction by condensing diethoxyethanal with 1,4-benzenebismethanamine, followed by ring closure with 20% oleum, and its spectral characteristics recorded. A similar reaction with diethyl 1,4-benzenebis(3-aminopropanoate) gave either 2,7-diaza-1,8-dimethylphenanthrene or 2,7-diaza-1,8-phenanthrenebis(methylsulphonic acid), depending on the conditions of the ring closure reaction. The bis methiodides of these compounds were tested for phospholipase A2 inhibitory action but were found to be inactive.
View MoreContact:+86-22-83718541
Address:32th Floor, Rongqiao Center Intersection of Changjiang Road and Nankai Six Road Nankai District Tianjin 300102, China
JinTan Pingsheng Chemical Co.,Ltd
Contact:+86-519-82828200
Address:NO.11Danfengxilu Road,Jintan City,Jiangsu,China
LIAOYANG WANRONG CHEMICALS COMPANY LIMITED
Contact:86-419-2390789
Address:XINLI VILLAGE , DONG NINGWEI COUNTY,TAIZIHE DISTRICT, LIAOYANG , LIAONING
Shanghai Yuanye Bio-Technology Co., Ltd.
website:http://www.shyuanye.com
Contact:+86-21-61845781
Address:Building 6, No. 465, Changta Road,Songjiang District,Shanghai,China
Sichuan WeiKeqi Biological Technology Co., Ltd.
Contact:86-028-81700200
Address:sichuan Chengdu Qingjiang Zhonglu 63号
Doi:10.1021/jo00175a049
(1984)Doi:10.1016/j.tet.2005.11.028
(2006)Doi:10.1055/s-1983-30502
(1983)Doi:10.1002/chem.201404316
(2014)Doi:10.1246/bcsj.57.823
(1984)Doi:10.1016/j.tet.2005.12.061
(2006)