Method for synthesis of 1,2,3,4,5,9-substituted benzazepine compound
A technology of benzazepine and synthesis method, which is applied in the field of organic compound process application, can solve problems such as no synthesis method proposed, and achieve the effect of promoting deep-level expansion, short route, and stable properties
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Embodiment 1
[0026]
[0027] Under the protection of inert gas, isatin compound 1a (0.2mmol) and alkyne compound 2a (1.0mmol) were dissolved in acetonitrile / 1,4-dioxane (2mL) (v / v=1:1), Add palladium acetate (0.02mmol), silver acetate (0.4mmol), under 100 DEG C of conditions, the reaction system was stirred for 12 hours, TLC detected, after the completion of the reaction, down to room temperature, dichloromethane extraction several times, combined organic phase, drying, The solvent was removed by rotation to obtain a crude product, and the product 3aa was obtained by flash column chromatography with a yield of 81%. 1 H NMR (300MHz, CDCl 3 ):δ=7.56(dd,J=7.3,1.2Hz,1H),7.23–6.92(m,18H),6.79–6.75(m,4H); 13 C NMR (75MHz, CDCl 3 ):δ=181.83,161.85,160.11,145.38,141.57,140.51,140.24,139.62,138.22,137.25,135.87,131.39,130.79,130.76,130.67,130.42,128.39,128.27,128.19,127.58,127.48,127.07,126.86, 126.27, 124.68, 121.71; HRMS (ESI) calculated value C 36 h 24 NO 2 [M+H] + 502.1802, actual val...
Embodiment 2
[0029]
[0030] The operation steps are the same as in Example 1, and the productive rate is 96%. 1H NMR (500MHz, CDCl 3 ):δ=7.37(s,1H),7.13-6.87(m,17H),6.72(m,4H),2.24(s,3H); 13 C NMR (125MHz, CDCl 3 ):δ=182.03,162.12,158.11,145.26,142.09,140.59,140.49,140.37,139.55,138.33,136.91,136.23,135.88,131.42,130.77,130.70,130.53,130.41,128.34,128.24,128.14,127.55,127.44, 127.41, 127.01, 126.79, 124.93, 121.79, 21.30; HRMS (ESI) calculated value C 37 h 26 NO 2 [M+H] + 516.1958, actual value 516.1965.
Embodiment 3
[0032]
[0033] The operation steps are the same as in Example 1, and the productive rate is 93%. 1H NMR (500MHz, CDCl3): δ=7.42(t, J=9.9Hz, 1H), 7.13–6.90(m, 17H), 6.79–6.72(m, 4H), 2.76(hept, J=6.9Hz, 1H ),1.14(d,J=6.9Hz,6H);13C NMR(125MHz,CDCl3):δ=182.14,162.05,158.30,147.15,145.00,140.57,140.42,140.39,139.71,138.36,136.90,135.940,131. 130.79,130.75,130.63,130.43,128.25,128.21,128.11,127.53,127.43,127.40,127.00,126.79,122.29,121.69,33.84,23.91;HRMS(ESI)计算值C39H30NO2[M+H]+544.2271,实际值544.2286 ..
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