501910-02-7Relevant articles and documents
Reaction of 3-arylaminobenzofuro-, 3-arylaminobenzothieno-, and 3-arylaminoindolo[2,3-c]pyrylium salts with nucleophilic reagents
Tolkunov,Vysotsky,Gorban',Shishkina,Shishkin,Dulenko
, p. 515 - 525 (2007/10/03)
We have studied the reactions of 3-arylaminobenzofuro-, 3-arylaminobenzothieno-, and 3-arylaminoindolo[2,3-c]pyrylium salts with ammonium acetate, primary amines, and hydrazine hydrate. In an alcoholic medium, primary amines and hydrazine hydrate open up
Acylation and cyclodehydration of benzofuran-, benzothiophene-, and indolyl-3-acetic acid arylamides. Synthesis of novel benzofuro[2,3-c]-, benzothieno[2,3-c], and indolo[2,3-c]pyrilium and pyridine derivatives
Tolkunov,Tolkunov,Dulenko
, p. 481 - 489 (2007/10/03)
The acylation of benzo[b]furan-, benzo[b]thiophene, and indolyl-3-acetic acid arylamides using acetic anhydride in the presence of 70% perchloric acid occurs at the α-position of the heterocycle to give 2-acetylbenzo[b]furan- , 2-acetylbenzo[b]thiophene,