3,4,5-,Trisubstituted-4,5-dihydroisoxazole, derivatives and their synthesis method and use
A technology of dihydroisoxazole and three substitutions, applied in derivatives and their synthesis,3,4, which can solve the problems of complicated steps and achieve the effect of simple reaction system, less reaction equipment and stable molecular structure
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Embodiment 1
[0135] The NMR and mass spectrometry data of embodiment 1 product are as follows:
[0136] 1H NMR (400MHz, CDCl3) δ7.69(dd, J=6.6,2.9Hz, 2H), 7.58(d, J=7.3Hz, 1H), 7.42–7.39(m,3H), 7.31–7.24(m, 3H), 6.05(dd, J=11.1, 6.9Hz, 1H), 3.96(dd, J=16.8, 11.2Hz, 1H), 3.23(dd, J=16.8, 6.9Hz, 1H).13C NMR (101MHz, CDCl3)δ156.13, 138.97, 131.11, 130.22, 129.47, 129.19, 129.03, 128.69, 127.18, 126.75, 126.61, 79.44, 77.32, 77.00, 76.68, 42.72. 258.06802, found 258.06799.
Embodiment 2
[0137] The NMR and mass spectrometry data of embodiment 2 product are as follows:
[0138] 1H NMR (400MHz, CDCl3) δ7.87(td, J=7.6, 1.6Hz, 1H), 7.56(dd, J=7.6, 1.6Hz, 1H), 7.41–7.35(m, 2H), 7.31–7.22( m,2H),7.18(td,J=8.0,1.2Hz,1H),7.12–7.07(m,1H),6.03(dd,J=11.2,7.2Hz,1H),4.06–3.98(m,1H) ,3.34–3.27(m,1H).13C NMR(101MHz,CDCl3)δ160.27(d,J=252.9Hz),152.97(d,J=3.1 Hz),138.78,131.84(d,J=8.6Hz) ,131.15,129.48,129.03,127.13,126.52,124.42(d,J=3.4Hz),117.28(d,J=11.6Hz),116.50,116.28,79.62(d,J=2.3Hz),77.32,77.00,76.68 ,44.26(d,J=6.8Hz).HRMS(ESI)m / z calcd for C15H12ClFNO+(M+H)+276.05860,found 276.05908.
Embodiment 3
[0139] The NMR and mass spectrum data of embodiment 3 product are as follows:
[0140] 1H NMR (400MHz, CDCl3) δ7.65–7.59(m,2H),7.41–7.23(m,6H),6.06(dd,J=11.0,7.1Hz,1H), 4.08(dd,J=17.3,11.0 Hz,1H),3.36(dd,J=17.2,7.1Hz,1H).13C NMR(101MHz,CDCl3)δ156.11,138.53,132.79,131.15,130.89,130.52,130.47,129.48,129.07,128.62,126.194,12 126.61,80.01,77.32,77.00, 76.68,44.92.HRMS(ESI)m / z calcd for C15H12Cl2NO+(M+H)+292.02905,found 292.02936.
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