Chem. J. Chinese Universities ›› 2021, Vol. 42 ›› Issue (9): 2766.doi: 10.7503/cjcu20210313
• Organic Chemistry • Previous Articles Next Articles
ZUO Huailong1, LEI Simin1, ZHANG Rui1, LI Yuxin2, CHEN Wei1()
Received:
2021-05-06
Online:
2021-09-10
Published:
2021-09-08
Contact:
CHEN Wei
E-mail:chenweicstq@163.com
Supported by:
CLC Number:
TrendMD:
ZUO Huailong, LEI Simin, ZHANG Rui, LI Yuxin, CHEN Wei. Design, Synthesis and Antifungal Activity of Novel Isoquinoline Derivatives[J]. Chem. J. Chinese Universities, 2021, 42(9): 2766.
Compd. | Appearance | Yield(%) | m. p./℃ | HRMS(cacld.), m/z[M-Br-]+ |
---|---|---|---|---|
Ia | Light yellow solid | 69.0 | 222—225 | 314.1539(314.1540) |
Ib | Light yellow solid | 66.6 | 187—188 | 330.1472(330.1489) |
Ic | Light yellow solid | 61.9 | 173—175 | 368.1275(368.1257) |
Id | Light yellow solid | 80.2 | 205—207 | 345.1235(345.1234) |
Ie | Light yellow solid | 63.9 | 238—240 | 325.1336(325.1336) |
If | Light yellow solid | 46.9 | 201—203 | 358.1418(358.1438) |
Ig | Light yellow solid | 67.5 | 221—223 | 376.1756(376.1696) |
Ih | Light yellow solid | 43.0 | 171—173 | 318.1282(318.1289) |
Ii | Light yellow solid | 43.7 | 238—240 | 336.1162(336.1194) |
Ij | Light yellow solid | 76.6 | 195—198 | 300.1357(300.1383) |
Ik | Light yellow solid | 65.0 | 217—219 | 334.0993(334.0994) |
Il | Light yellow solid | 77.9 | 173—175 | 300.1357(300.1383) |
Im | Light yellow solid | 75.9 | 203—205 | 334.0979(334.0994) |
In | Light yellow solid | 71.3 | 194—196 | 316.1157(316.1155) |
Io | Light yellow solid | 80.8 | 170—173 | 348.1059(348.1053) |
Compd. | Appearance | Yield(%) | m. p./℃ | HRMS(cacld.), m/z[M-Br-]+ |
---|---|---|---|---|
Ia | Light yellow solid | 69.0 | 222—225 | 314.1539(314.1540) |
Ib | Light yellow solid | 66.6 | 187—188 | 330.1472(330.1489) |
Ic | Light yellow solid | 61.9 | 173—175 | 368.1275(368.1257) |
Id | Light yellow solid | 80.2 | 205—207 | 345.1235(345.1234) |
Ie | Light yellow solid | 63.9 | 238—240 | 325.1336(325.1336) |
If | Light yellow solid | 46.9 | 201—203 | 358.1418(358.1438) |
Ig | Light yellow solid | 67.5 | 221—223 | 376.1756(376.1696) |
Ih | Light yellow solid | 43.0 | 171—173 | 318.1282(318.1289) |
Ii | Light yellow solid | 43.7 | 238—240 | 336.1162(336.1194) |
Ij | Light yellow solid | 76.6 | 195—198 | 300.1357(300.1383) |
Ik | Light yellow solid | 65.0 | 217—219 | 334.0993(334.0994) |
Il | Light yellow solid | 77.9 | 173—175 | 300.1357(300.1383) |
Im | Light yellow solid | 75.9 | 203—205 | 334.0979(334.0994) |
In | Light yellow solid | 71.3 | 194—196 | 316.1157(316.1155) |
Io | Light yellow solid | 80.8 | 170—173 | 348.1059(348.1053) |
Compd. | 1H NMR(CDCl3, 400 MHz, TMS), δ | 13C NMR(CDCl3, 100 MHz, TMS), δ |
---|---|---|
Ia | 10.32(s, 1H), 8.46(d, J=7.3 Hz, 1H), 8.11—8.03(m, 2H), 7.73(td, J=7.6, 1.1 Hz, 1H), 7.42(t, J=7.6 Hz, 1H), 7.42—7.35(m, 3H), 7.31(d, J=7.6 Hz, 1H), 7.13(dd, J=7.8, 1.9 Hz, 1H), 7.03—6.97(m, 2H), 4.61(t, J=7.9 Hz, 2H), 3.52(t, J=7.9 Hz, 2H), 2.32(s, 3H) | 165.4, 158.9, 154.9, 150.5, 136.2, 134.1, 132.8, 130.3, 130.2, 128.6, 128.2, 128.1, 126.2, 119.2, 109.2, 108.7, 105.0, 53.6, 28.0, 20.9 |
Ib | 10.33(s, 1H), 8.45(d, J=7.3 Hz, 1H), 8.11—8.03(m, 2H), 7.72(td, J=7.6, 1.1 Hz, 1H), 7.44(t, J=7.6 Hz, 1H), 7.41—7.34(m, 3H), 7.30(d, J=7.6 Hz, 1H), 7.13(dd, J=7.8, 1.9 Hz, 1H), 7.03—6.97(m, 2H), 4.60(t, J=7.9 Hz, 2H), 3.71(s, 3H), 3.51(t, J=7.9 Hz, 2H) | 159.4, 155.9, 155.8, 150.2, 136.0, 135.0, 133.3, 130.3, 129.0, 128.4, 126.5, 126.1, 124.5, 120.6, 120.5, 114.9, 114.8, 55.7, 53.4, 28.4 |
Ic | 10.39(s, 1H), 8.45(d, J=7.6 Hz, 1H), 7.93(dd, J=8.1, 1.8 Hz, 1H), 7.70(td, J=7.6, 1.2 Hz, 1H), 7.61(d, J=8.6 Hz, 2H), 7.56—7.49(m, 2H), 7.43(t, J=7.1 Hz, 1H), 7.37(d, J=7.6 Hz, 1H), 7.15(d, J=8.5 Hz, 2H), 7.11(dd, J=8.2, 1.9 Hz, 1H), 4.56(t, J=7.9 Hz, 2H), 3.50(t, J=7.9 Hz, 2H) | 166.6, 158.8, 157.4, 143.7, 139.0, 136.9, 136.3, 132.0, 128.90, 128.08, 127.6(JC—F=23.7 Hz), 126.1(JC—F=273 Hz), 125.71, 125.3, 121.5, 119.2, 118.6, 113.5, 51.8, 25.9 |
Id | 10.45(s, 1H), 8.45(d, J=7.7 Hz, 1H), 8.25—8.18(m, 2H), 7.95(dd, J=8.1, 2.2 Hz, 1H), 7.78—7.68(m, 2H), 7.61(t, J=8.2 Hz, 1H), 7.45(t, J=7.7 Hz, 1H), 7.38(d, J=7.6 Hz, 1H), 7.19—7.14(m, 3H), 4.60(t, J=7.9 Hz, 2H), 3.53(t, J=7.9 Hz, 2H) | 166.9, 161.7, 156.4, 144.0, 143.7, 139.2, 137.0, 136.4, 132.3, 129.1, 128.2, 126.4, 125.8, 122.6, 119.5, 118.6, 114.7, 77.2, 51.9, 26.0 |
Ie | 10.41(s, 1H), 8.44(d, J=7.2 Hz, 1H), 7.90(dd, J=8.1, 1.8 Hz, 1H), 7.73(td, J=7.6, 1.3 Hz, 1H), 7.66—7.60(m, 3H), 7.56(t, J=8.2 Hz, 1H), 7.44(t, J=7.6, Hz, 1H), 7.38(d, J=7.6 Hz, 1H), 7.20—7.13(m, 3H), 4.56(t, J=7.9 Hz, 2H), 3.51(t, J=7.9 Hz, 2H) | 168.0, 148.1, 136.3, 135.9, 135.1, 134.1, 134.0, 133.8, 130.7, 130.4, 129.2, 128.6, 128.2, 127.8, 126.6, 118.9, 117.3, 105.1, 53.2, 22.6 |
If | 10.36(s, 1H), 8.46(d, J=7.1 Hz, 1H), 8.06—7.99(m, 2H), 7.96(dd, J=8.2, 1.6 Hz, 1H), 7.71(td, J=7.6, 1.4 Hz, 1H), 7.58—7.50(m, 2H), 7.44(t, J=7.1 Hz, 1H), 7.37(d, J=7.6 Hz, 1H), 7.13(dd, J=7.9, 1.9 Hz, 1H), 7.09—7.04(m, 2H), 4.55(t, J=7.9 Hz, 2H), 3.88(s, 3H), 3.50(t, J=7.9 Hz, 2H) | 166.8, 150.3, 136.4, 136.1, 133.9, 131.8, 131.7, 130.6, 128.6, 128.6, 128.1, 126.3, 117.3, 116.8, 111.4, 110.9, 107.3, 106.3, 53.4, 52.1, 27.0 |
Ig | 10.30(s, 1H), 8.46(d, J=7.7 Hz, 1H), 7.86(dd, J=7.8, 2.1 Hz,1H), 7.71—7.62(m, 1H), 7.57—7.52(m, 3H), 7.51—7.50(m, 1H), 7.49—7.45(m, 2H), 7.42—7.37(m, 3H), 7.35(d, J=7.6 Hz, 1H), 7.33—7.29(m, 1H), 7.11—7.04(m, 3H), 4.52(t, J=7.9 Hz, 2H), 3.47(t, J=7.9 Hz, 2H) | 166.4, 158.8, 155.1, 143.6, 140.1, 139.0, 137.7, 136.9, 136.4, 131.9, 128.9, 128.9, 128.8, 128.2, 127.4, 127.0, 125.7, 120.5, 120.2, 117.6, 112.3, 51.9, 26.0 |
Compd. | 1H NMR(CDCl3, 400 MHz, TMS), δ | 13C NMR(CDCl3, 100 MHz, TMS), δ |
Ih | 10.36(s, 1H), 8.50(d, J=7.8 Hz, 1H), 7.84(d, J=7.8, 1.8 Hz, 1H), 7.72(t, J=7.6 Hz, 1H), 7.53—7.45(m, 2H), 7.40—7.35(m, 2H), 7.09—7.07(m, 4H), 7.04(dd, J=8.3, 2.2 Hz, 1H), 4.52(t, J=7.9 Hz, 2H), 3.50(t, J=7.9 Hz, 2H) | 166.6, 159.7(JC—F=243.8 Hz), 159.4, 151.3, 143.7, 139.0, 137.1, 136.2, 132.0, 129.2, 128.1, 125.9, 121.8(JC—F=8.4 Hz), 120.1, 117.3(JC—F=22.1 Hz), 116.9, 111.6, 51.8, 26.1 |
Ii | 10.37(s, 1H), 8.46(d, J=7.7 Hz, 1H), 8.01(dd, J=7.4, 1.9 Hz, 1H), 7.73(td, J=7.6, 1.3 Hz, 1H), 7.63(t, J=2.3 Hz, 1H), 7.56(t, J=8.2 Hz, 1H), 7.45(t, J=7.1 Hz, 1H), 7.40(d, J=7.6 Hz, 1H), 7.14(dd, J=8.2, 2.2 Hz, 1H), 6.62—6.52(m, 3H), 4.59(t, J=7.9 Hz, 2H), 3.54(t, J=7.9 Hz, 2H) | 166.5, 163.7(JC—F=234.0 Hz), 158.1(JC—F=13.7 Hz), 157.00, 143.8, 139, 136.9, 136.4, 132.1, 128.9, 128.1, 125.8, 121.5, 119.1, 113.8, 102.8(JC—F=28.6 Hz), 99.9(JC—F=25.7 Hz), 53.24, 27.61 |
Ij | 10.25(s, 1H), 8.44(d, J=7.8 Hz, 1H), 8.06—7.98(m, 2H), 7.68(td, J=7.6, 1.3 Hz, 1H), 7.44—7.34(m, 4H), 7.22—7.17(m, 1H), 7.07—7.00(m, 4H), 4.57(t, J=7.9 Hz, 2H), 3.49(t, J=7.9 Hz, 2H) | 165.1, 160.2, 155.3, 138.7, 136.8, 136.6, 136.1, 130.3, 129.0, 128.1, 125.8, 125.1, 124.6, 120.3, 118.9, 52.0, 26.1 |
Ik | 10.31(s, 1H), 8.45(d, J=7.6 Hz, 1H), 8.09—8.03(m, 2H), 7.73—7.67(m, 1H), 7.43(t, J=7.6 Hz, 1H), 7.40—7.32(m, 3H), 7.09—7.03(m, 2H), 7.01—6.95(m, 2H), 4.58(t, J=7.9 Hz, 2H), 3.50(t, J=7.9 Hz, 2H) | 165.3, 159.7, 154.0, 138.7, 137.2, 136.6, 136.1, 130.4, 130.2, 128.9, 128.1, 125.8, 124.8, 121.5, 119.1, 52.0, 26.1 |
Il | 10.14(s, 1H), 8.41(d, J=7.7 Hz, 1H), 8.05—8.02(m, 1H), 7.49—7.44(m, 1H), 7.43—7.38(m, 1H), 7.32(t, J=8.3 Hz, 2H), 7.27—7.23(m, 3H), 7.10—7.07(m, 2H), 6.99—6.95(m, 2H), 4.45(t, J=6.8 Hz, 2H), 3.35(t, J=6.8 Hz, 2H) | 193.0, 148.7, 142.9, 141.8, 141.2, 133.8, 133.7, 131.8, 129.7, 128.4, 126.2, 124.8, 122.4, 119.6, 117.3, 116.8, 111.5, 44.8, 33.9 |
Im | 10.25(s, 1H), 8.44(d, J=7.7 Hz, 2H), 8.06—7.98(m, 2H), 7.68(d, J=7.6 Hz, 2H), 7.45—7.38(m, 3H), 7.23—7.17(m, 1H), 7.08—7.00(m, 3H), 4.57(t, J=7.9 Hz, 2H), 3.49(t, J=7.9 Hz, 2H) | 165.1, 160.2, 155.3, 138.7, 136.8, 136.6, 136.1, 130.3, 129.0, 128.1, 125.8, 125.1, 124.6, 120.3, 118.9, 52.0, 26.1 |
In | 9.50(s, 1H), 8.44(d, J=7.7 Hz, 1H), 8.11(dd, J=7.7, 1.3 Hz, 1H), 7.66(td, J=7.7, 1.3 Hz, 1H), 7.53—7.45(m, 1H), 7.44—7.35(m, 3H), 7.31(d, J=7.6 Hz, 1H), 7.23—7.17(m, 3H), 7.15—7.09(m, 2H), 4.34(t, J=7.9 Hz, 2H), 3.39(t, J=7.9 Hz, 2H) | 169.4, 143.2, 138.9, 136.6, 136.3, 134.2, 133.1, 131.8, 130.7, 130.4, 130.3, 130.0, 128.7, 128.4, 128.3, 127.4, 125.3, 53.1, 26.1 |
Io | 10.13(s, 1H), 8.40(d, J=7.7 Hz, 1H), 8.05—8.02(m, 1H), 7.77—7.72(m, 2H), 7.54—7.52(m, 2H), 7.50—7.45(m, 1H), 7.43—7.38(m, 2H), 7.37—7.29(m, 2H), 7.05—7.01(m, 2H), 4.42(t, J=5.8 Hz, 2H), 3.26(t, J=5.7 Hz, 2H) | 193.2, 146.9, 142.1, 141.1, 135.5, 134.7, 134.2, 134.1, 133.1, 132.1, 130.7, 129.1, 127.5, 126.8, 121.2, 116.3, 112.5, 44.3, 32.8 |
Compd. | 1H NMR(CDCl3, 400 MHz, TMS), δ | 13C NMR(CDCl3, 100 MHz, TMS), δ |
---|---|---|
Ia | 10.32(s, 1H), 8.46(d, J=7.3 Hz, 1H), 8.11—8.03(m, 2H), 7.73(td, J=7.6, 1.1 Hz, 1H), 7.42(t, J=7.6 Hz, 1H), 7.42—7.35(m, 3H), 7.31(d, J=7.6 Hz, 1H), 7.13(dd, J=7.8, 1.9 Hz, 1H), 7.03—6.97(m, 2H), 4.61(t, J=7.9 Hz, 2H), 3.52(t, J=7.9 Hz, 2H), 2.32(s, 3H) | 165.4, 158.9, 154.9, 150.5, 136.2, 134.1, 132.8, 130.3, 130.2, 128.6, 128.2, 128.1, 126.2, 119.2, 109.2, 108.7, 105.0, 53.6, 28.0, 20.9 |
Ib | 10.33(s, 1H), 8.45(d, J=7.3 Hz, 1H), 8.11—8.03(m, 2H), 7.72(td, J=7.6, 1.1 Hz, 1H), 7.44(t, J=7.6 Hz, 1H), 7.41—7.34(m, 3H), 7.30(d, J=7.6 Hz, 1H), 7.13(dd, J=7.8, 1.9 Hz, 1H), 7.03—6.97(m, 2H), 4.60(t, J=7.9 Hz, 2H), 3.71(s, 3H), 3.51(t, J=7.9 Hz, 2H) | 159.4, 155.9, 155.8, 150.2, 136.0, 135.0, 133.3, 130.3, 129.0, 128.4, 126.5, 126.1, 124.5, 120.6, 120.5, 114.9, 114.8, 55.7, 53.4, 28.4 |
Ic | 10.39(s, 1H), 8.45(d, J=7.6 Hz, 1H), 7.93(dd, J=8.1, 1.8 Hz, 1H), 7.70(td, J=7.6, 1.2 Hz, 1H), 7.61(d, J=8.6 Hz, 2H), 7.56—7.49(m, 2H), 7.43(t, J=7.1 Hz, 1H), 7.37(d, J=7.6 Hz, 1H), 7.15(d, J=8.5 Hz, 2H), 7.11(dd, J=8.2, 1.9 Hz, 1H), 4.56(t, J=7.9 Hz, 2H), 3.50(t, J=7.9 Hz, 2H) | 166.6, 158.8, 157.4, 143.7, 139.0, 136.9, 136.3, 132.0, 128.90, 128.08, 127.6(JC—F=23.7 Hz), 126.1(JC—F=273 Hz), 125.71, 125.3, 121.5, 119.2, 118.6, 113.5, 51.8, 25.9 |
Id | 10.45(s, 1H), 8.45(d, J=7.7 Hz, 1H), 8.25—8.18(m, 2H), 7.95(dd, J=8.1, 2.2 Hz, 1H), 7.78—7.68(m, 2H), 7.61(t, J=8.2 Hz, 1H), 7.45(t, J=7.7 Hz, 1H), 7.38(d, J=7.6 Hz, 1H), 7.19—7.14(m, 3H), 4.60(t, J=7.9 Hz, 2H), 3.53(t, J=7.9 Hz, 2H) | 166.9, 161.7, 156.4, 144.0, 143.7, 139.2, 137.0, 136.4, 132.3, 129.1, 128.2, 126.4, 125.8, 122.6, 119.5, 118.6, 114.7, 77.2, 51.9, 26.0 |
Ie | 10.41(s, 1H), 8.44(d, J=7.2 Hz, 1H), 7.90(dd, J=8.1, 1.8 Hz, 1H), 7.73(td, J=7.6, 1.3 Hz, 1H), 7.66—7.60(m, 3H), 7.56(t, J=8.2 Hz, 1H), 7.44(t, J=7.6, Hz, 1H), 7.38(d, J=7.6 Hz, 1H), 7.20—7.13(m, 3H), 4.56(t, J=7.9 Hz, 2H), 3.51(t, J=7.9 Hz, 2H) | 168.0, 148.1, 136.3, 135.9, 135.1, 134.1, 134.0, 133.8, 130.7, 130.4, 129.2, 128.6, 128.2, 127.8, 126.6, 118.9, 117.3, 105.1, 53.2, 22.6 |
If | 10.36(s, 1H), 8.46(d, J=7.1 Hz, 1H), 8.06—7.99(m, 2H), 7.96(dd, J=8.2, 1.6 Hz, 1H), 7.71(td, J=7.6, 1.4 Hz, 1H), 7.58—7.50(m, 2H), 7.44(t, J=7.1 Hz, 1H), 7.37(d, J=7.6 Hz, 1H), 7.13(dd, J=7.9, 1.9 Hz, 1H), 7.09—7.04(m, 2H), 4.55(t, J=7.9 Hz, 2H), 3.88(s, 3H), 3.50(t, J=7.9 Hz, 2H) | 166.8, 150.3, 136.4, 136.1, 133.9, 131.8, 131.7, 130.6, 128.6, 128.6, 128.1, 126.3, 117.3, 116.8, 111.4, 110.9, 107.3, 106.3, 53.4, 52.1, 27.0 |
Ig | 10.30(s, 1H), 8.46(d, J=7.7 Hz, 1H), 7.86(dd, J=7.8, 2.1 Hz,1H), 7.71—7.62(m, 1H), 7.57—7.52(m, 3H), 7.51—7.50(m, 1H), 7.49—7.45(m, 2H), 7.42—7.37(m, 3H), 7.35(d, J=7.6 Hz, 1H), 7.33—7.29(m, 1H), 7.11—7.04(m, 3H), 4.52(t, J=7.9 Hz, 2H), 3.47(t, J=7.9 Hz, 2H) | 166.4, 158.8, 155.1, 143.6, 140.1, 139.0, 137.7, 136.9, 136.4, 131.9, 128.9, 128.9, 128.8, 128.2, 127.4, 127.0, 125.7, 120.5, 120.2, 117.6, 112.3, 51.9, 26.0 |
Compd. | 1H NMR(CDCl3, 400 MHz, TMS), δ | 13C NMR(CDCl3, 100 MHz, TMS), δ |
Ih | 10.36(s, 1H), 8.50(d, J=7.8 Hz, 1H), 7.84(d, J=7.8, 1.8 Hz, 1H), 7.72(t, J=7.6 Hz, 1H), 7.53—7.45(m, 2H), 7.40—7.35(m, 2H), 7.09—7.07(m, 4H), 7.04(dd, J=8.3, 2.2 Hz, 1H), 4.52(t, J=7.9 Hz, 2H), 3.50(t, J=7.9 Hz, 2H) | 166.6, 159.7(JC—F=243.8 Hz), 159.4, 151.3, 143.7, 139.0, 137.1, 136.2, 132.0, 129.2, 128.1, 125.9, 121.8(JC—F=8.4 Hz), 120.1, 117.3(JC—F=22.1 Hz), 116.9, 111.6, 51.8, 26.1 |
Ii | 10.37(s, 1H), 8.46(d, J=7.7 Hz, 1H), 8.01(dd, J=7.4, 1.9 Hz, 1H), 7.73(td, J=7.6, 1.3 Hz, 1H), 7.63(t, J=2.3 Hz, 1H), 7.56(t, J=8.2 Hz, 1H), 7.45(t, J=7.1 Hz, 1H), 7.40(d, J=7.6 Hz, 1H), 7.14(dd, J=8.2, 2.2 Hz, 1H), 6.62—6.52(m, 3H), 4.59(t, J=7.9 Hz, 2H), 3.54(t, J=7.9 Hz, 2H) | 166.5, 163.7(JC—F=234.0 Hz), 158.1(JC—F=13.7 Hz), 157.00, 143.8, 139, 136.9, 136.4, 132.1, 128.9, 128.1, 125.8, 121.5, 119.1, 113.8, 102.8(JC—F=28.6 Hz), 99.9(JC—F=25.7 Hz), 53.24, 27.61 |
Ij | 10.25(s, 1H), 8.44(d, J=7.8 Hz, 1H), 8.06—7.98(m, 2H), 7.68(td, J=7.6, 1.3 Hz, 1H), 7.44—7.34(m, 4H), 7.22—7.17(m, 1H), 7.07—7.00(m, 4H), 4.57(t, J=7.9 Hz, 2H), 3.49(t, J=7.9 Hz, 2H) | 165.1, 160.2, 155.3, 138.7, 136.8, 136.6, 136.1, 130.3, 129.0, 128.1, 125.8, 125.1, 124.6, 120.3, 118.9, 52.0, 26.1 |
Ik | 10.31(s, 1H), 8.45(d, J=7.6 Hz, 1H), 8.09—8.03(m, 2H), 7.73—7.67(m, 1H), 7.43(t, J=7.6 Hz, 1H), 7.40—7.32(m, 3H), 7.09—7.03(m, 2H), 7.01—6.95(m, 2H), 4.58(t, J=7.9 Hz, 2H), 3.50(t, J=7.9 Hz, 2H) | 165.3, 159.7, 154.0, 138.7, 137.2, 136.6, 136.1, 130.4, 130.2, 128.9, 128.1, 125.8, 124.8, 121.5, 119.1, 52.0, 26.1 |
Il | 10.14(s, 1H), 8.41(d, J=7.7 Hz, 1H), 8.05—8.02(m, 1H), 7.49—7.44(m, 1H), 7.43—7.38(m, 1H), 7.32(t, J=8.3 Hz, 2H), 7.27—7.23(m, 3H), 7.10—7.07(m, 2H), 6.99—6.95(m, 2H), 4.45(t, J=6.8 Hz, 2H), 3.35(t, J=6.8 Hz, 2H) | 193.0, 148.7, 142.9, 141.8, 141.2, 133.8, 133.7, 131.8, 129.7, 128.4, 126.2, 124.8, 122.4, 119.6, 117.3, 116.8, 111.5, 44.8, 33.9 |
Im | 10.25(s, 1H), 8.44(d, J=7.7 Hz, 2H), 8.06—7.98(m, 2H), 7.68(d, J=7.6 Hz, 2H), 7.45—7.38(m, 3H), 7.23—7.17(m, 1H), 7.08—7.00(m, 3H), 4.57(t, J=7.9 Hz, 2H), 3.49(t, J=7.9 Hz, 2H) | 165.1, 160.2, 155.3, 138.7, 136.8, 136.6, 136.1, 130.3, 129.0, 128.1, 125.8, 125.1, 124.6, 120.3, 118.9, 52.0, 26.1 |
In | 9.50(s, 1H), 8.44(d, J=7.7 Hz, 1H), 8.11(dd, J=7.7, 1.3 Hz, 1H), 7.66(td, J=7.7, 1.3 Hz, 1H), 7.53—7.45(m, 1H), 7.44—7.35(m, 3H), 7.31(d, J=7.6 Hz, 1H), 7.23—7.17(m, 3H), 7.15—7.09(m, 2H), 4.34(t, J=7.9 Hz, 2H), 3.39(t, J=7.9 Hz, 2H) | 169.4, 143.2, 138.9, 136.6, 136.3, 134.2, 133.1, 131.8, 130.7, 130.4, 130.3, 130.0, 128.7, 128.4, 128.3, 127.4, 125.3, 53.1, 26.1 |
Io | 10.13(s, 1H), 8.40(d, J=7.7 Hz, 1H), 8.05—8.02(m, 1H), 7.77—7.72(m, 2H), 7.54—7.52(m, 2H), 7.50—7.45(m, 1H), 7.43—7.38(m, 2H), 7.37—7.29(m, 2H), 7.05—7.01(m, 2H), 4.42(t, J=5.8 Hz, 2H), 3.26(t, J=5.7 Hz, 2H) | 193.2, 146.9, 142.1, 141.1, 135.5, 134.7, 134.2, 134.1, 133.1, 132.1, 130.7, 129.1, 127.5, 126.8, 121.2, 116.3, 112.5, 44.3, 32.8 |
Compd. | Antifungal activity(%) | |||||
---|---|---|---|---|---|---|
A. solani | F. graminearum | S. sclerotiorum | R. solani | P. piricola | R. cerealis | |
Ia | 17.6 | 27.8 | 14.3 | 22.2 | 52.6 | 52.3 |
Ib | 11.8 | 13.9 | 26.8 | 11.1 | 57.9 | 70.8 |
Ic | 17.6 | 55.6 | 7.1 | 61.1 | 97.4 | 96.9 |
Id | 17.6 | 36.1 | 66.1 | 13.9 | 71.1 | 82.4 |
Ie | 35.3 | 55.6 | 85.7 | 66.7 | 94.7 | 93.8 |
If | 17.6 | 19.4 | 8.9 | 27.8 | 60.5 | 35.4 |
Ig | 35.3 | 47.2 | 48.2 | 55.6 | 57.9 | 93.8 |
Ih | 29.4 | 27.8 | 76.8 | 13.9 | 31.6 | 67.3 |
Ii | 29.4 | 44.4 | 44.6 | 36.1 | 57.9 | 66.2 |
Ij | 17.6 | 22.2 | 39.3 | 11.1 | 84.2 | 36.9 |
Ik | 17.6 | 13.9 | 17.9 | 13.9 | 52.6 | 58.5 |
Il | 64.7 | 83.3 | 91.3 | 91.7 | 94.7 | 96.9 |
Im | 29.4 | 36.1 | 32.1 | 52.8 | 71.1 | 70.8 |
In | 23.5 | 41.7 | 30.4 | 27.8 | 57.9 | 78.5 |
Io | 17.6 | 52.8 | 32.1 | 55.6 | 57.9 | 81.5 |
Chlorothalonil | 90.9 | 57.7 | 100 | 91.1 | 92.3 | 100 |
Sanguinarine | 54.5 | 64.2 | 90.3 | 64.7 | 82.3 | 79.8 |
Compd. | Antifungal activity(%) | |||||
---|---|---|---|---|---|---|
A. solani | F. graminearum | S. sclerotiorum | R. solani | P. piricola | R. cerealis | |
Ia | 17.6 | 27.8 | 14.3 | 22.2 | 52.6 | 52.3 |
Ib | 11.8 | 13.9 | 26.8 | 11.1 | 57.9 | 70.8 |
Ic | 17.6 | 55.6 | 7.1 | 61.1 | 97.4 | 96.9 |
Id | 17.6 | 36.1 | 66.1 | 13.9 | 71.1 | 82.4 |
Ie | 35.3 | 55.6 | 85.7 | 66.7 | 94.7 | 93.8 |
If | 17.6 | 19.4 | 8.9 | 27.8 | 60.5 | 35.4 |
Ig | 35.3 | 47.2 | 48.2 | 55.6 | 57.9 | 93.8 |
Ih | 29.4 | 27.8 | 76.8 | 13.9 | 31.6 | 67.3 |
Ii | 29.4 | 44.4 | 44.6 | 36.1 | 57.9 | 66.2 |
Ij | 17.6 | 22.2 | 39.3 | 11.1 | 84.2 | 36.9 |
Ik | 17.6 | 13.9 | 17.9 | 13.9 | 52.6 | 58.5 |
Il | 64.7 | 83.3 | 91.3 | 91.7 | 94.7 | 96.9 |
Im | 29.4 | 36.1 | 32.1 | 52.8 | 71.1 | 70.8 |
In | 23.5 | 41.7 | 30.4 | 27.8 | 57.9 | 78.5 |
Io | 17.6 | 52.8 | 32.1 | 55.6 | 57.9 | 81.5 |
Chlorothalonil | 90.9 | 57.7 | 100 | 91.1 | 92.3 | 100 |
Sanguinarine | 54.5 | 64.2 | 90.3 | 64.7 | 82.3 | 79.8 |
1 | Dong X. P., Natural Medicinal Chemistry, China Press of Traditional Medicine, Beijing, 2016, 50—52(董小萍. 天然药物化学, 北京: 中国中医药出版社, 2016, 50—52) |
2 | Shang X. F., Yang C. J., Morris⁃Natschke S. L., Li J. C., Yin X. D., Liu Y. Q., Guo X., Peng J. W., Goto M., Zhang J. Y., Lee K. H., Med. Res. Rev., 2020, 40(6), 2212—2289 |
3 | Zhang R., Guo Q., Kennelly E. J., Long C., Chai X., Fitoterapia, 2020, 146, 104697 |
4 | Qing Z. X., Yang P., Tang Q., Cheng P., Liu X. B., Zheng Y. J., Liu Y. S., Zeng J. G., Curr. Org. Chem., 2017, 21(18), 1920—1934 |
5 | Wei Q. H., Study on the Inhibition Mechanism of Chelerythrine and Its Derivatives Against Plant Pathogens, Northeast Forestry University, Haerbin, 2020(韦庆慧. 白屈菜红碱及其衍生物对植物病原菌的抑制机理研究, 哈尔滨: 东北林业大学, 2020) |
6 | Liu H., Wang J., Zhao J., Lu S., Wang J., Jiang W., Zhou L., Nat. Prod. Comm., 2009, 4(11), 1557—1560 |
7 | Yang X. J., Miao F., Yao Y., Cao F. J., Yang R., Ma Y. N., Qin B. F., Zhou L., Molecules, 2012, 17(11), 13026—13035 |
8 | Lv P., Chen Y., Shi T., Wu X., Li Q X., Hua R., Pestic. Biochem. Phys., 2018, 147, 3—10 |
9 | Yang R., Gao Z. F., Zhao J. Y., Li W. B., Zhou L., Miao F., J. Agric. Food Chem., 2015, 63(7), 1906—1914 |
10 | Chen W., Zuo H. L., Li Y. X., Liu J., Zhou X. L., Chin. J. Org., 2019, 39(8), 2317—2322(陈伟, 左怀龙, 李玉新, 刘江, 周先礼. 有机化学, 2019, 39(8), 2317—2322) |
11 | Chen T., Xiong H., Yang J. F., Zhu X. L., Qu R. Y., Yang G. F., J. Agric. Food Chem., 2020, 68(37), 9839—9877 |
12 | Li H., Wu Y., Gao M. Q., Zhu X. L., Yang G. F., Mod. Agrochem., 2020, 19(1), 14—20, 23(李华, 武园, 高梦琪, 朱晓磊, 杨光富. 现代农药, 2020, 19(1), 14—20, 23) |
13 | Gao Q., Chen B., Hou X. M., Bai Y. J., Song Y., Tang X. S., Chem. J. Chinese Universities, 2015, 36(1), 93—101(高旗, 陈邦, 侯晓萌, 白银娟, 宋阳, 唐雪松. 高等学校化学学报, 2015, 36(1), 93—101) |
14 | Li P., Chen Y., Xia R. J., Guo T., Zhang M., Jiang S. C., Tang X., He M., Xue W., Chem. J. Chinese Universities, 2019, 40(5), 909—917(李普, 陈英, 夏榕娇, 郭涛, 张敏, 蒋仕春, 汤旭, 贺鸣, 薛伟. 高等学校化学学报, 2019, 40(5), 909—917) |
15 | Correia M., Rodrigues M., Paíga P., Delerue⁃Matos C., Fungicides, Academic Press, Oxford, 2016, 130—168 |
16 | Wu S. K., Shi J., Chen J. X., Hu D. Y., Zang L. S., Song B. A., J. Agric. Food Chem., 2021, 69(16), 4645—4654 |
17 | Maiti D., Buchwald S. L., J. Am. Chem. Soc., 2009, 131(47), 17423—17429 |
18 | Li H. G., Zhao Y. Y., Sun P. W., Gao L., Xiong L. X., Yang N., Zhou S., Li Y. X., Li Z. M., Chem. Res. Chinese Universities, 2021, 37(3), 655—661 |
19 | Chen W., Li Y. X., Zhou Y. Y., Ma Y., Li Z. M., Chin. Chem. Lett., 2019, 30(12), 2160—2162 |
[1] | ZHANG Aiqin, WANG Man, SHEN Gangyi, JIN Jun. Interactions Between Polybrominated Diphenyl Ethers and Human Serum Albumin Using SPR and Molecular Docking [J]. Chem. J. Chinese Universities, 2020, 41(9): 2054. |
[2] | HE Feng,BAI Jinhai,CHEN Shuxian,TAN Xiaobei. Antifungal Activity and Mechanism of an Essential Oil from Eremothecium ashbyii† [J]. Chem. J. Chinese Universities, 2019, 40(2): 272. |
[3] | MU Boshuai, CHANG Suna, BIAN Yanqing, LI Yuan. Asymmetric Synthesis and Antibacterial Activity of Chiral 2-Methoxycarbonyl-4-fluorophenyl-1,5-benzothiazepines† [J]. Chem. J. Chinese Universities, 2017, 38(3): 413. |
[4] | CHEN Wei, WEI Wei, LIU Ming, HUA Xuewen, LI Yuxin, LI Yonghong, ZHANG Xiao, LI Zhengming. Design, Synthesis and Biological Activity of Novel Sulfonylurea Derivatives Containing Dimethoxymethyl-substituted Pyrimidine Moiety† [J]. Chem. J. Chinese Universities, 2015, 36(7): 1291. |
[5] | CHEN Wei, WEI Wei, ZHOU Sha, LI Yonghong, ZHANG Xiao, TONG Jun, LI Yuxin, LI Zhengming. Design, Synthesis and Biological Activity of Novel Sulfonylurea Derivatives Containing Phenyl-substituted Pyrimidine Moiety† [J]. Chem. J. Chinese Universities, 2015, 36(4): 672. |
[6] | ZHANG Jing, MU Boshuai, WU Meng, BIAN Yanqing, LI Yuan. Synthesis, Antifungal Activity and Structure-activity Relationship of -Fluorophenyl-2,3-dihydro-1,5-benzothiazepines Derivatives† [J]. Chem. J. Chinese Universities, 2015, 36(4): 687. |
[7] | DONG Lu, YI Zhongsheng, WU Zhiwei, WANG Haiyang, ZHANG Aiqian. Mechanism Study on the Interaction Between 2'-Hydroxy-2,4-dibromo Diphenyl Ethers and Human Serum Albumin Based on Spectroscopic Methods and Computional Simulations† [J]. Chem. J. Chinese Universities, 2015, 36(3): 516. |
[8] | WANG Cuiling, HOU Baolong, ZHANG Ning, SUN Yanni, LIU Jianli. Biomimetic Synthesis of Natural Product Tryptanthrin and Its Derivatives† [J]. Chem. J. Chinese Universities, 2015, 36(2): 274. |
[9] | GAO Qi, CHEN Bang, HOU Xiaomeng, BAI Yinjuan, SONG Yang, TANG Xuesong. Synthesis of Novel Dipyrimidinone Diphenyl Ethers† [J]. Chem. J. Chinese Universities, 2015, 36(1): 93. |
[10] | KANG Wang, BU Huijuan, LI Wenhong, LI Yuan. Preliminary Structure-activity Relationship of 2-Ethoxycarbonyl-4-aryl-1,5-benzothiazepines with Antifungal Activity† [J]. Chem. J. Chinese Universities, 2014, 35(4): 766. |
[11] | FAN Shili, ZHANG Bo, GAO Liye, WANG Lanzhi, BIAN Yanqing, LI Yuan. Synthesis, Antifungal Activity and Structure-activity Relationship of 2-Methoxycarbonyl/ethoxycarbonyl-4-fluorophenyl-1,5-benzothiazepines† [J]. Chem. J. Chinese Universities, 2014, 35(12): 2574. |
[12] | LIU Zhuo, PAN Li, YU Shu-Jing, LI Zheng-Ming. Synthesis and Antifungal Activity of N-(4'-Substituted aromatic pyrimidin-2'-yl)-2-ethoxycarbonyl phenyl Sulfonylurea Derivatives [J]. Chem. J. Chinese Universities, 2013, 34(8): 1868. |
[13] | QIU Zhao-Lai, LI Wen-Hong, ZHU Hai-Fei, LIU Qian, LI Yuan. Synthesis, Crystal Structure and Antifungal Activities of 3-(CH2)nCO2C2H5-1,5-Benzothiazepines [J]. Chem. J. Chinese Universities, 2013, 34(3): 579. |
[14] | ZHAO Lian, YUAN Xiang-Guo, ZHAO Jian-Peng, CHEN Hua*, LIU Li, LI Xiao-Liu, CAO Ke-Qiang. Design, Synthesis and Antifungal Activity Against Valsa Mali of the Triamino Substitued Triazines Bearing Aminopyrimidine Group [J]. Chem. J. Chinese Universities, 2011, 32(12): 2795. |
[15] | ZHAO LiNa WANG XiuYan KONG ZhiGuo WANG ZiChen. Biomimetic Synthesis of Dendrite-shaped Aragonite Calcium Carbonate Particles and Application in PVC [J]. Chem. J. Chinese Universities, 2010, 31(12): 2329. |
Viewed | ||||||
Full text |
|
|||||
Abstract |
|
|||||