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Microwave assisted synthesis of 2,3-dihydro-4H-benzo[4,5]thiazolo [3,2-a]furo[2,3-d] pyrimidin-4-ones by radical addition of 2-hydroxy-4H-benzo[4,5]thiazolo[3,2-a] pyrimidin-4-ones to various conjugated alkenes and dienes mediated Mn(OAc)(3)

Yilmaz, Mehmet; Inal, Asl i Ustalar


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{
  "DOI": "10.1016/j.tet.2022.132806", 
  "abstract": "Synthesis of chemically important, novel 2,3-dihydro-4H-benzo [4,5]thiazolo [3,2-a]furo [2,3-d]pyr-imidin-4-one derivatives was approached in this work. These heterocyclic compounds were synthesized in good to excellent yields from the reaction of Mn(OAc)3 mediated radical addition of 2-hydroxy-4H- benzo [4,5]thiazolo [3,2-a]pyrimidin-4-one (1a-1f) derivatives to various conjugated alkenes (2a-2e, 2h) and dienes (2f, 2g, 2i) under microwave irradiation in mild conditions. Also, a different compound skeleton, 2,3-dihydrobenzo [4,5]imidazo [1,2-a]furo [2,3-d]pyrimidin-4(10H)-one 3a (90%), was obtained from the reaction of 2-hydroxy-10-methylbenzo [4,5]imidazo [1,2-a]pyrimidin-4(10H)-one (1g) and 1,1diphenylethylene (2h) for the first time. While no product was obtained with conventional method in radical addition reactions, dihydrofuropyrimidines (3a-z, 3a) were synthesized in excellent yields using microwave irradiating method at 150 ?, 350 W for 60 s. All isolated compounds were characterized by spectroscopic techniques (FTIR, H-1 NMR, C-13 NMR and( 19)F NMR) and HRMS analysis.(c) 2022 Elsevier Ltd. All rights reserved.", 
  "author": [
    {
      "family": "Yilmaz", 
      "given": " Mehmet"
    }, 
    {
      "family": "Inal", 
      "given": " Asl i Ustalar"
    }
  ], 
  "container_title": "TETRAHEDRON", 
  "id": "260157", 
  "issued": {
    "date-parts": [
      [
        2022, 
        1, 
        1
      ]
    ]
  }, 
  "title": "Microwave assisted synthesis of 2,3-dihydro-4H-benzo[4,5]thiazolo [3,2-a]furo[2,3-d] pyrimidin-4-ones by radical addition of 2-hydroxy-4H-benzo[4,5]thiazolo[3,2-a] pyrimidin-4-ones to various conjugated alkenes and dienes mediated Mn(OAc)(3)", 
  "type": "article-journal", 
  "volume": "116"
}
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