Chem. J. Chinese Universities ›› 1998, Vol. 19 ›› Issue (S1): 210.
• Organic Synthesis Chemistry • Previous Articles Next Articles
Guang-Fu YANG, Hua-Zheng YANG
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Abstract: 5-Amino-3-benzyl (aryl)thio-1,2,4-triazoles and its analogues (pyrazole) 1 are important intermediates for the syntheses of a lot of biological active compounds[1,2]. In our previous paper[3], we reported the regioselective addition of 1 with aryl isocyanates and the experimental results showed that the orientation of the addition of 5-amino-3-benzyl (aryl)thio-1,2,4-triazoles and its analogues with the aryl isocyanates can be directed by controlling the reaction temperature.The 1-position adduct 2 was obtained regiospecifically below 120℃, whereas the 5-position adduct 3 was obtained selectively when the reaction temperature was raised to 170℃ (Scheme 1).
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Guang-Fu YANG, Hua-Zheng YANG. Regioselective Addition of 5-Amino-l,2,4-Triazoles and Its Analogues with Arylsulfonyl Isocyanates[J]. Chem. J. Chinese Universities, 1998, 19(S1): 210.
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http://www.cjcu.jlu.edu.cn/EN/Y1998/V19/IS1/210