HRID1642580
反应详情
EQUATION
反应方程式
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反应物
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产物
PROCEDURE
实验过程
The title compound was prepared from Compound 225 by using an analogous procedure to that outlined in the preparation of Compound 64. 1H NMR (400 MHz, Methanol-d4) δ 8.36 (s, 1 H) 8.12 (s, 1 H) 8.08 (m, 1 H) 7.97 (m, 1 H) 7.88 (t, J=7.84 Hz, 1 H) 7.69 (s, 1 H) 7.21 (d, J=8.32 Hz, 1 H) 7.16 (d, J=8.32 Hz, 1 H) 4.65 (m, 2 H) 4.42 (t, J=6.08 Hz, 2 H) 4.14 (q, J=7.32Hz, H) 3.36 (q, J=7.6 Hz, 2 H) 2.39 (m, 2 H) 1.55 (d, J=7.32 Hz, 3 H) 1.33 (t, J=7.6 Hz, 3 H). [M+H] calc'd for C25H27ClN3O5S, 516; found, 516.