Synthesis of 1-amino- and 1-hydroxy-9,10-anthraquinone derivatives based on reaction sequences between 2-acetyl-1,4-naphthoquinone and enamines

Citation
K. Kobayashi et al., Synthesis of 1-amino- and 1-hydroxy-9,10-anthraquinone derivatives based on reaction sequences between 2-acetyl-1,4-naphthoquinone and enamines, TETRAHEDR L, 41(14), 2000, pp. 2381-2384
Citations number
25
Categorie Soggetti
Chemistry & Analysis","Organic Chemistry/Polymer Science
Journal title
TETRAHEDRON LETTERS
ISSN journal
00404039 → ACNP
Volume
41
Issue
14
Year of publication
2000
Pages
2381 - 2384
Database
ISI
SICI code
0040-4039(20000401)41:14<2381:SO1A1D>2.0.ZU;2-3
Abstract
2-Acetyl-1,4-naphthoquinone was treated with pyrrolidine (or morpholine) en amines, derived from cyclic and acyclic ketones, in DMF at room temperature for 24-72 h to afford 3,4-disubstituted 1-pyrrolidino(or morpholino)-9,10- anthraquinones. On the other hand, when the treatment of 2-acetyl-1,4-napht hoquinone with enamines for 2 min was followed by addition of water and hea ting at 100 degrees C for 2 h, the corresponding 1-hydroxy-9,10-naphthoquin one derivatives were obtained. (C) 2000 Elsevier Science Ltd. All rights re served.