5118-94-5Relevant articles and documents
Ring Closure Reactions of Methyl N-(Haloacetyl)anthranilates with Ammonia
Cho, Nam Sook,Song, Ki Youn
, p. 1807 - 1810 (2007/10/02)
In the presence of ammonia, methyl N-(bromoacetyl)anthranilate (4) is cyclized into 3H-1,4-benzodiazepine-2,5(1H,4H)-dione (1).However, when 4 is replaced with methyl N-(chloroacetyl)anthranilate (6), the only heterocyclic product formed in the reaction is 2-(chloromethyl)quinazoline-4(3H)-one (7).Under analogous conditions, 3-haloacetamidocrotonates (9,10) do not yield any heterocyclic products and no 1,4-diazepines can be obtained.