
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:86-898-65311214
Address:Room 102, BLDG. 68 Jiangnan City, No. 66 Heping Road,Haikou, Hainan, China
Contact:+86-731-84427351
Address:154 JIANXIANG SOUTH ROAD
Purestar Chem Enterprise Co.,Ltd
website:http://www.purestarchem.com
Contact:05722157374
Address:no235.huanchengdong Rd
Laizhou City Laiyu Chemical CO.,Ltd
Contact:+86-535-2719337/2719339
Address:Chenggang road zhuyou laizhou City Shangdong China
Beijing Zhongshuo Pharmaceutical T & D Co.,Ltd
Contact:0086-10-64430626
Address:ea No 16, HEPINGLI,DONGCHENG DISTRICT,BEIJING,P.R.CHINA.
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)