Nucleophilic Substitutions of 2-Halonaphtho[2,3-b]furan-4,9-diones and 2-Nitronaphtho[2,3-b]furan-4,9-dione

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概要

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• 2-Chloronaphtho[2,3-b]furan-4,9-dione (4) was allowed to react with sodium phenoxide to produce 2-phenoxynaphtho[2,3-b]furan-4,9-dione (8) in 55% yield. Also, in a similar manner, 8 was obtained from the reactions of 2-bromonaphtho[2,3-b]furan-4,9-dione (5), 2-iodonaphtho[2,3-b]furan-4,9-dione (6) and 2-nitronaphtho[2,3-b]furan-4,9-dione (7) with sodium phenoxide. The reaction of 4 with sodium methoxide gave methyl 3-hydroxy-1,4-naphthoquinone-2-acetate (9) in which the furan ring was cleaved. 2-Phenylthionaphtho[2,3-b]furan-4,9-dione (11) and 2-methylthionaphtho[2,3-b]furan-4,9-dione (12) were obtained from the reactions of 4 with thiolates in 63% and 62% yields, respectively. Furthermore, 4 was treated with sodiomalonic ester ot give diethyl 2-(naphtho[2,3-b]furan-4,9-dione-2-yl)malonate (13) in 28% yield. Compound 13 was also obtained from the reactions of 5 and 7 with sodiomalonic ester. All these nucleophilic substitutions were carried out at room temperature. It was found that 4-7 had a high reactivity with various nucleophilic reagents.

• 公益社団法人日本薬学会の論文
• 1997-10-15

著者

• Tanaka A

  Faculty Of Pharmaceutical Sciences Tokyo University Of Science

• TANAKA Akira

  Faculty of Agriculture, Hokkaido University

• Yamamoto K

  Faculty Of Pharmaceutical Sciences Josai University

• KOYANAGI Jyunichi

  Faculty of Pharmaceutical Sciences, Josai University

• NAKAYAMA Kouji

  Faculty of Pharmaceutical Sciences, Josai University

• YAMAMOTO Katsumi

  Faculty of Pharmaceutical Sciences, Josai University

• Nakayama K

  Faculty Of Pharmaceutical Sciences Josai University

• Koyanagi J

  Faculty Of Pharmaceutical Sciences Josai University

• Koyanagi Jyunichi

  Faculty Of Pharmaceutical Sciences Josai International University

• Tanaka Akira

  Faculty Of Agriculture Hokkaido University

• Yamamoto Katsumi

  Faculty Of Pharmaceutical Sciences Josai University

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