Aqua mediated synthesis of substituted 2-amino-4H-chromenes catalyzed by green and reusable Preyssler heteropolyacid

Bioorganic and Medicinal Chemistry Letters

Volumn 17, Issue 15, 2007, Pages 4262-4265

  Heravi, Majid M ^a   Bakhtiari, Khadijeh ^a   Zadsirjan, Vahideh ^a   Bamoharram, Fatemeh F ^b   Heravi, Omid M ^c  

^a ALZAHRA UNIVERSITY   (Iran)

^b ISLAMIC AZAD UNIVERSITY   (Iran)

^c ISLAMIC AZAD UNIVERSITY   (Iran)

Author keywords

H14 NaP5W30O110 ; Heteropolyacid; Preyssler; Substituted 2 amino 4H chromenes; Water

Indexed keywords

2 AMINO 4H CHROMENE; CHROMENE DERIVATIVE; UNCLASSIFIED DRUG; WATER;

ARTICLE; CATALYSIS; DRUG SYNTHESIS;

ACIDS; BENZOPYRANS; CATALYSIS; WATER;

EID: 34447108076     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bmcl.2007.05.023     Document Type: Article

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54. 110] (0.03 g), in water (5 mL) were refluxed for 3 h; After completion of the reaction which was monitored by TLC, the mixture was cooled to room temperature. The precipitate was collected by filtration and recrystallized from MeOH. In order to show generality of the procedure, the reaction was repeated with other benzaldehyde derivatives. The results are summarized in Table 1.Recyclibility of the catalyst: After evaporating of water the catalyst was filtered, washed with diethyl ether, dried at 130 °C for 1 h, and re-used in another reaction.