Polycyclic Aromatic Compounds ( IF 2.4 ) Pub Date : 2020-12-01 , DOI: 10.1080/10406638.2020.1852269 Amit Kumar 1 , Kuldeep Mahiya 2 , Ashok K. Prasad 1 , Sunil K. Singh 3
Abstract
One pot multi-component strategy has been developed for the synthesis of a small library of nineteen 4-aryl-1,4-dihydro-oxochromeno[3,2-b]oxoindeno[6,5-e]pyridine by the condensation of 4-aminocoumarin, aromatic aldehyde and indane-1,3-dione in acetic acid:ethylene glycol (5:1) in good yields along with the formation of di-(4-aminocoumarin-3-yl)arylmethane as by product in three cases. The use of microwave irradiation for the condensation of 4-aminocoumarin, aromatic aldehyde and indane-1,3-dione in acetic acid and ethylene glycol at 200 W and at 120 °C led to the selective formation of 4-aryl-1,4-dihydro-oxochromeno[3,2-b]oxoindeno[6,5-e] pyridine in excellent yields. Interestingly, the side product di-(4-aminocoumarin-3-yl)arylmethane could be converted exclusively to 4-(4'-nitrophenyl)-1,4-dihydro-di(oxochromeno[3,2-b:5,6-e])pyridine on microwave irradiation under identical condition.
中文翻译:
4-Aryl-1,4-Dihydro-Oxochromeno[3,2-b] Oxoindeno[6,5-e]吡啶的多组分合成
已开发出一锅多组分策略,用于通过 4-芳基-1,4-二氢-氧代色基[3,2-b]氧代茚并[6,5-e]吡啶的缩合合成小库-氨基康...