HRID1710975
反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
PROCEDURE
实验过程
Starting from the compound 183 and following the procedure described above for the synthesis of compound 159 (scheme 30, step 4, example 121), title compound 184 was obtained in 66% yield. 1H NMR (400 MHz, DMSO-d6) δ ppm: 8.45(d, J=5.6 Hz, 1H), 8.33(s, 1H), 8.00 (s, 1H), 7.85-7.75 (m, 1H), 7.69 (s, 1H), 7.39(t, J=8.4 Hz, 1H), 7.35-7.28 (m, 1H), 7.28-7.22 (m, 1H), 7.22(d, J=7.6 Hz, 1H), 6.97(d, J=8.4 Hz, 1H), 6.89(t, J=7.6 Hz, 1H), 6.57(d, J=5.6 Hz, 1H), 4.19(t, J=6.4 Hz, 2H), 3.82 (s, 2H), 3.77 (s, 3H), 2.88(t, J=6.4 Hz, 2H), 2.28 (s, 3H).