Please use this identifier to cite or link to this item:
Title: Synthesis of 5H-dibenzo(b,f)azepine-5-carboxylic acid [3-chloro-2-(substitutedphenyl)-4-oxoazetidin-1-yl]amide from 5H-dibenzo(b,f) azepine-5-carbonyl chloride
Authors: Bhatt, Pralav V
Patel, Pravin M
Keywords: 5H-dibenzo(b,f)azepine-5-carbonyl chloride
5H-dibenzo(b,f)azepine-5-acid hydrazide
5H-dibenzo­(b,f)aze­pine-5-carboxylic acid (4-methoxybenzylidene)-hydrazide
5H-dibenzo(b,f)azepine-5-carboxylic acid [3-chloro-2-(4-methoxyphenyl)-4-oxoazetidin-1-yl]amide
Issue Date: Oct-2005
Publisher: CSIR
Series/Report no.:  Int.Cl.7 C 07 D
Abstract: 5H-Dibenzo(b,f)azepine-5-carbonyl chloride 1 has been prepared from 5H-dibenzo(b,f)azepine by phosgenation, which has been then treated with hydrazine hydrate to give 5H-dibenzo(b,f)azepine-5-acid hydrazide 2. It has been reacted with various aromatic aldehydes to afford 5H-dibenzo(b,f)azepine-5-carboxylic acid-(substitutedbenzylidene)hydrazide 3a-j. The synthesis of 5H-dibenzo(b,f)azepine-5-carboxylic acid [3-chloro-2-(substitutedphenyl)-4-oxoazetidin-1-yl]amide 4a-j has been achieved by the reaction of 3 with chloroacetyl chloride in presence of triethylamine. The products have been characterized by elemental analysis, IR, 1H NMR and mass spectral studies.
Description: 2082-2086
ISSN: 0975-0983(Online); 0376-4699(Print)
Appears in Collections:IJC-B Vol.44B(10) [October 2005]

Files in This Item:
File Description SizeFormat 
IJCB 44B(10) 2082-2086.pdf155.98 kBAdobe PDFView/Open

Items in NOPR are protected by copyright, with all rights reserved, unless otherwise indicated.