Study on the Mass Spectrometry of 3-Aryl 4-benzoyl-1-ethoxylcarbonyl-1α-phenyl-1,1α,2,3,-tetrahydro-4H-azirino-[1,2-α][1,5] benzodiazepine[J]. Journal of Chinese Mass Spectrometry Society, 2002, 23(3): 141-141.
Citation: Study on the Mass Spectrometry of 3-Aryl 4-benzoyl-1-ethoxylcarbonyl-1α-phenyl-1,1α,2,3,-tetrahydro-4H-azirino-[1,2-α][1,5] benzodiazepine[J]. Journal of Chinese Mass Spectrometry Society, 2002, 23(3): 141-141.

Study on the Mass Spectrometry of 3-Aryl 4-benzoyl-1-ethoxylcarbonyl-1α-phenyl-1,1α,2,3,-tetrahydro-4H-azirino-1,2-α1,5 benzodiazepine

  • On EI-MS, the saturated oxygen atom of the ethoxylcarbonyl group is capable of acting as site to which a hydrogen atom can be transferred, the presence of hydrogen on an azirino gives a product ion corresponding to the loss of alcohol. Seven memberd ring of diazepine decomposes by α-cleavage follow by 2-ehlorophezyl or 2-chlorophenylethylene elimination gives benzamidazole or quinoxaline.
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