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Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/71

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
Authors: Pathak, Richa
Nag, Somnath
Batra, Sanjay
Keywords: 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.
Issue Date: 2006
Citation: Synthesis (2006), 4205-4211
Series/Report no.: CDRI Communication No. 7050.
Abstract: 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..
URI: http://hdl.handle.net/123456789/71
Appears in Collections:Medicinal and Process Chemistry

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