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A Facile synthesis of 3-Methylene-4-aryl-1,3,4,5-tetrahydro-benzo[b][1,4] di-azepin-2-ones and 3-arylemethylene-4,5-dihydro-3H-benzo[b][1,4]diazepin-2-ylamines

IR@CDRI: CSIR-Central Drug Research Institute, Lucknow

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Field Value
 
Creator Pathak, Richa
Nag, Somnath
Batra, Sanjay
 
Date 2007-12-29T08:16:48Z
2007-12-29T08:16:48Z
2006
 
Identifier Synthesis (2006), 4205-4211
http://hdl.handle.net/123456789/71
 
Description A simple and convenient synthesis of 3-methylene-4-aryl-1,3,4,5-tetrahydro-benzo[b][1,4] diazepin-2-ones was accomplished by the SN2 nucleophilic substitution of the acetates of Baylis-Hillman adducts of acrylate with 1,2-phenylenediamines followed by base-mediated intramolecular cyclization. On the other hand similar substrates derived from the Baylis-Hillman adducts of acrylonitrile via Pinner’s reaction leads to 3-arylmethylene-4,5-dihydro-3H-benzo[b][1,4]diazepin-2-ylamines in good yields..
 
Format 148400 bytes
application/pdf
 
Language en
 
Relation CDRI Communication No. 7050.
 
Subject Baylis-Hillman
1,2-phenylenediamine
3-Methylene-4-aryl-1
3,4,5-tetrahydro-benzo[b][1,4] diazepin-2-ones
3-arylmethylene-4,5-dihydro-3H-benzo[b][1,4]diazepin-2-ylamines.
 
Title A Facile synthesis of 3-Methylene-4-aryl-1,3,4,5-tetrahydro-benzo[b][1,4] di-azepin-2-ones and 3-arylemethylene-4,5-dihydro-3H-benzo[b][1,4]diazepin-2-ylamines
 
Type Article