6533b831fe1ef96bd1299afb

RESEARCH PRODUCT

Synthesis of substituted isoindolo[2,1-a]quinoxalin-6-yl–amino and 6-imino-5-yl thiourea derivatives

Anna CarboneVirginia SpanòGirolamo CirrincioneBarbara ParrinoPatrizia DianaCristina CianciminoChandrakant SarwadeAlessandra MontalbanoSpanòPaola Barraja

subject

lcsh:QD241-441chemistry.chemical_compoundThiourealcsh:Organic chemistryChemistry1-a]quinoxalinesOrganic Chemistryisoindolo[21-a]quinoxalinesisoindolo[2; 1-a]quinoxalinesMedicinal chemistryisoindolo[2

description

A series of substituted 1-(5-bromopyridin-2-yl)-3-[2-(isoindolo[2,1-a]quinoxalin-6- ylamino)ethyl]thiourea and 1-(5-bromopyridin-2-yl)-3-[2-(6-iminoisoindolo[2,1-a]quinoxalin- 5(6H)-yl)ethyl]thiourea derivatives were prepared in good yields (63-85%) by reaction between the corresponding amino compounds with 5-bromo-2-isothiocyanatopyridine. All thiourea derivatives, tested for inhibition of HIV-1 RT, showed no significant antiviral activity.

10.3998/ark.5550190.p008.858https://www.arkat-usa.org/arkivoc-journal/browse-arkivoc/ark.5550190.p008.858