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JIANG Jun-hang, Lü Jia-guo, ZHOU You-jun. Improvement of the synthetic process of 7-azaindol-3-carboxylic acid[J]. Journal of Pharmaceutical Practice and Service, 2007, (5): 312-314,345.
Citation: JIANG Jun-hang, Lü Jia-guo, ZHOU You-jun. Improvement of the synthetic process of 7-azaindol-3-carboxylic acid[J]. Journal of Pharmaceutical Practice and Service, 2007, (5): 312-314,345.

Improvement of the synthetic process of 7-azaindol-3-carboxylic acid

  • Received Date: 2007-03-21
  • Objective : To improve the synthetic process of 7-azaindol-3-carboxylic acid. Methods : The succinonitrile was taken as the original raw material.The isopropyl ether,n-heptane,and chlorobenzene, which were used in original technics,were subsituted by ethyl acetate,petroleun ether,and xylene respectively.The disposition technics was optimized. Results : The technics was successfully improved due to its low cost,small toxicity,convenient disposition and high yield. Conclusions : The higher overall yields was 43.4%.This improved method is more suitable for industrial production for its low cost.
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    沈阳化工大学材料科学与工程学院 沈阳 110142

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Improvement of the synthetic process of 7-azaindol-3-carboxylic acid

Abstract: Objective : To improve the synthetic process of 7-azaindol-3-carboxylic acid. Methods : The succinonitrile was taken as the original raw material.The isopropyl ether,n-heptane,and chlorobenzene, which were used in original technics,were subsituted by ethyl acetate,petroleun ether,and xylene respectively.The disposition technics was optimized. Results : The technics was successfully improved due to its low cost,small toxicity,convenient disposition and high yield. Conclusions : The higher overall yields was 43.4%.This improved method is more suitable for industrial production for its low cost.

JIANG Jun-hang, Lü Jia-guo, ZHOU You-jun. Improvement of the synthetic process of 7-azaindol-3-carboxylic acid[J]. Journal of Pharmaceutical Practice and Service, 2007, (5): 312-314,345.
Citation: JIANG Jun-hang, Lü Jia-guo, ZHOU You-jun. Improvement of the synthetic process of 7-azaindol-3-carboxylic acid[J]. Journal of Pharmaceutical Practice and Service, 2007, (5): 312-314,345.

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