
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 MoreChongqing Werlchem Fine Chemical Co. Ltd
Contact:+86-23-67521957
Address:NO.15,Fortune Road,Yubei District,401121,Chongqing,China
Contact:18669908765
Address:Zibo City, Shandong Province, P.R.China
Shanghai Run-Biotech Co., Ltd.
website:http://www.run-biotech.com
Contact:+86-21-31576854/57171705 / 57171706
Address:second floor, building 3, No.999, jiangyue Road, minghang District, Shanghai, China
Neworld Chemical Co., Ltd Shanghai(expird)
Contact:+86-21-62202658
Address:11F, Blvd 2, No. 1969 PuXing Rd, Shanghai
website:http://www.tcfinechem.com/
Contact:18681346930
Address:baifu town,whou district
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)