期刊文献+

苯并色烯类化合物合成方法的探讨

The Exploration of the Synthetic Method for Benzochromenopyrimidine Derivatives
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摘要 以取代苯甲醛、丙二腈和2-萘酚(或2,7-萘二酚)为原料合成出了3-氨基-2-氰基-1-(4-取代苯基)-1H-苯并[f]色烯类物质,后者在冰醋酸或者醋酸钠催化作用下,乙酸酐中回流,合成出苯并色烯并嘧啶类化合物。这类化合物的关环反应条件易于实施,后处理简单,易于纯化,属于首次报道。 A series of benzo [f] chromeno [2, 3-d] pyrimidine derivatives were prepared using acetic acid or sodium acetate as catalyst by the condensationcyclization reaction of acetic anhydride and 2- amino-3-cyanobenzo [f] chromene derivatives which were synthesized by the reaction of substitutedbenzoaldehyde, malononitrile and naphthalen-2-ol. This cyclization reaction of 2-amino-3- cyanobenzo [f] chromene derivatives could be finished easily and the product was easily purified, and this method is reported for the first time.
出处 《中山大学学报(自然科学版)》 CAS CSCD 北大核心 2009年第2期66-70,共5页 Acta Scientiarum Naturalium Universitatis Sunyatseni
基金 广东省科技厅科技计划资助项目(2003C103006 2007B060401068) 国家重点实验室开放课题资助项目(2007-01)
关键词 合成 苯并[f]色烯类化合物 苯并[f]色烯并嘧啶类化合物 benzo [f] chromene derivatives benzo[f] chromeno [ 2, 3-d] pyrimidine derivatives
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  • 1CAI S X, ZHANG H, JIANG S C, et al. Preparation of substituted 4H-chromenes and analogs as activators of caspases and inducers of apoptosis and their uses against cancer and other disorders [ P]. WO 2002092594,2002.
  • 2SHANKAR G, SOLOW-CORDERO D, SPENCER J V, et al. Methods of treating conditions associated with an Edg-3 receptor [ P]. U.S. 2004167185, 20040826.
  • 3SHANKAR G, SOLOW-CORDERO D, SPENCER J V, et al. Methods using Edg receptor modulators for the treatment of Edg receptor-associated conditions [ P]. WO 2003062392, 2003.
  • 4KEMNITZER W, KASIBHATLA S, JIANG S. Discovery of 4-aryl-4H- chromenes as a new series of apoptosis in- ducers using a cell- and caspase-based high-throughput screening assay. 2. Structure-activity relationships of the 7- and 5-, 6-, 8-positions [ J ]. Bioorganic & Medicinal Chemistry Letters, 2005, 15 : 4745 -4751.
  • 5KEMNITZER W, DREWE J, JIANG S. Discovery of 4- Aryl-4H-chromenes as a new series of apoptosis inducers using a cell- and caspase-based high-throughput screening assay, structure-activity relationships of the 4-aryl group [J]. J Med Chem, 2004, 47:6299 -6310.
  • 6FUJII N, YAMASHITA Y, MIZUKAMI T, et al. Correlation between the formation of cleavable complex with to- poisomerase I and growth-inhibitory activity for saintopintype antibiotics [ J ]. Molecular Pharmacology, 1997, 51 (2) : 269 - 276.
  • 7MARTIN P, RODIER S, MONDON M, et al. Synthesis and cytotoxic activity of tetracenomycin d and of saintopin analogues [ J ]. Bioorganic & Medicinal Chemistry, 2001, 10(2): 253-260.
  • 8LAUGHLIN M, THORNE T L. Methods for treating vascular disruption disorders [ P]. WO 2008124828, 2008.
  • 9LAUGHLIN M. Preparation of N- ( 4-methoxyphenyl ) -N- methyl-N-(2- methylquinazolin-4-yl) amine hydrochloride for treatment of melanoma [ P]. WO 2008124823, 2008.
  • 10BECK H P, KOHN T, RUBENSTEIN S, et al. Discovery of potent LPA2 (EDG4) antagonists as potential an- ticancer agents [ J ]. Bioorganic & Medicinal Chemistry Letters, 2008, 18(3) : 1037 -1041.

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