The synthesis of some N,N-disubstituted 4-amino-5,6-dihydro-3-phenyl-2H-thieno[2,3-h]-1-benzopyran-2-ones (4a-f), by reaction of phenylchloroketene with a series of N,N-disubstituted (E)-5-aminomethylene-6,7-dihydrobenzo[b]thiophen-4(5)-ones, followed by dehydrochlorination in situ of the primary adducts with DBN, is described. A moderate local anaesthetic activity was observed in the title compounds, particularly in 4e.

Download full-text PDF

Source
http://dx.doi.org/10.1016/s0014-827x(01)01116-8DOI Listing

Publication Analysis

Top Keywords

synthesis nn-disubstituted
8
nn-disubstituted 4-amino-56-dihydro-3-phenyl-2h-thieno[23-h]-1-benzopyran-2-ones
8
4-amino-56-dihydro-3-phenyl-2h-thieno[23-h]-1-benzopyran-2-ones synthesis
4
4-amino-56-dihydro-3-phenyl-2h-thieno[23-h]-1-benzopyran-2-ones 4a-f
4
4a-f reaction
4
reaction phenylchloroketene
4
phenylchloroketene series
4
series nn-disubstituted
4
nn-disubstituted e-5-aminomethylene-67-dihydrobenzo[b]thiophen-45-ones
4
e-5-aminomethylene-67-dihydrobenzo[b]thiophen-45-ones dehydrochlorination
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!