高等学校化学学报 ›› 2026, Vol. 47 ›› Issue (10): 20260151.doi: 10.7503/cjcu20260151
收稿日期:2026-04-14
出版日期:2026-10-10
发布日期:2026-06-04
通讯作者:
杨家强
E-mail:yjqcn@126.com
作者简介:第一联系人:共同第一作者.
基金资助:
YAN Yu1, LU Zicong2, WANG Qing2, YANG Jiaqiang2(
)
Received:2026-04-14
Online:2026-10-10
Published:2026-06-04
Contact:
YANG Jiaqiang
E-mail:yjqcn@126.com
Supported by:摘要:
为了获取抗菌候选化合物, 以天然产物3-methylcarbazole为起始化合物, 对其结构进行修饰及优化, 设计合成了系列含异噁唑片段的3-methylcarbazole衍生物; 利用核磁共振氢谱(1H NMR)、 碳谱(13C NMR)和 元素分析确定了其结构. 抗菌活性测试结果表明, 该类化合物对金黄色葡萄球菌(S. aureus)、 表皮葡萄球 菌(S. epidermidis)和耐甲氧西林金黄色葡萄球菌(MRSA)具有较好的抑制作用, 大部分衍生物的抗菌活性优于 3-methylcarbazole; 尤其以化合物3q最为突出, 对三者的最小抑菌浓度(MIC)分别为0.5, 1和2 μg/mL, 抗S. aureus和S. epidermidis活性与对照药相当, 抗MRSA活性远优于对照药. 时间-杀菌曲线显示, 化合物3q在4×MIC时, 对S. aureus整个生长周期具有快速杀菌作用; 分子对接结果表明, 化合物3q与靶蛋白GyrB有较好的结合作用; 同时, 化合物3q对小鼠单核巨噬细胞无明显毒性. 综上, 异噁唑片段的引入能够提高3-methylcarbazole的抗菌活性.
中图分类号:
TrendMD:
颜瑜, 卢子聪, 汪晴, 杨家强. 含异噁唑片段的3-Methylcarbazole衍生物的设计、 合成与抗菌活性. 高等学校化学学报, 2026, 47(10): 20260151.
YAN Yu, LU Zicong, WANG Qing, YANG Jiaqiang. Design, Synthesis and Antibacterial Activities of 3-Methylcarbazole Derivatives Containing Isoxzole. Chem. J. Chinese Universities, 2026, 47(10): 20260151.
| Compd. | Appearance | Yield(%) | m. p./℃ | Elemental analysis(%), calcd.(found) | ||
|---|---|---|---|---|---|---|
| C | H | N | ||||
| 3a | White solid | 63 | 162—163 | 81.63(81.50) | 5.36(5.39) | 8.28(8.41) |
| 3b | White solid | 58 | 148—149 | 81.79(81.66) | 5.72(5.77) | 7.95(7.85) |
| 3c | White solid | 59 | 149—150 | 81.79(81.87) | 5.72(5.58) | 7.95(8.02) |
| 3d | White solid | 48 | 124—126 | 77.51(77.62) | 4.81(4.75) | 7.86(7.96) |
| 3e | White solid | 54 | 145—146 | 77.51(77.65) | 4.81(4.76) | 7.86(7.70) |
| 3f | White solid | 52 | 137—138 | 77.51(77.43) | 4.81(4.70) | 7.86(7.77) |
| 3g | White solid | 44 | 172—173 | 74.09(73.91) | 4.60(4.68) | 7.51(7.37) |
| 3h | White solid | 47 | 196—197 | 74.09(74.13) | 4.60(4.62) | 7.51(7.55) |
| 3i | White solid | 43 | 106—107 | 66.20(66.33) | 4.11(4.20) | 6.71(6.64) |
| 3j | White solid | 44 | 121—123 | 66.20(66.41) | 4.11(3.98) | 6.71(6.63) |
| 3k | White solid | 33 | 202—203 | 72.05(71.96) | 4.47(4.55) | 10.96(11.04) |
| Compd. | Appearance | Yield(%) | m. p./℃ | Elemental analysis(%), calcd.(found) | ||
| C | H | N | ||||
| 3l | White solid | 70 | 153—154 | 72.88(73.00) | 5.65(5.49) | 6.54(6.41) |
| 3m | White solid | 55 | 141—142 | 70.40(70.62) | 3.85(3.91) | 7.14(7.23) |
| 3n | White solid | 59 | 115—117 | 73.23(73.04) | 4.68(4.60) | 8.13(8.21) |
| 3o | White solid | 60 | 151—153 | 73.72(73.53) | 5.06(4.97) | 7.82(7.89) |
| 3p | White solid | 59 | 124—125 | 77.17(77.22) | 5.30(5.36) | 8.18(8.26) |
| 3q | White solid | 50 | 164—166 | 67.32(67.47) | 3.44(3.53) | 6.83(6.95) |
| 3r | White solid | 36 | 151—152 | 67.32(67.20) | 3.44(3.53) | 6.83(6.98) |
| 3s | White solid | 56 | 148—149 | 68.24(68.09) | 4.06(3.98) | 6.63(6.52) |
Table 1 Physical properties of compounds 3a—3s
| Compd. | Appearance | Yield(%) | m. p./℃ | Elemental analysis(%), calcd.(found) | ||
|---|---|---|---|---|---|---|
| C | H | N | ||||
| 3a | White solid | 63 | 162—163 | 81.63(81.50) | 5.36(5.39) | 8.28(8.41) |
| 3b | White solid | 58 | 148—149 | 81.79(81.66) | 5.72(5.77) | 7.95(7.85) |
| 3c | White solid | 59 | 149—150 | 81.79(81.87) | 5.72(5.58) | 7.95(8.02) |
| 3d | White solid | 48 | 124—126 | 77.51(77.62) | 4.81(4.75) | 7.86(7.96) |
| 3e | White solid | 54 | 145—146 | 77.51(77.65) | 4.81(4.76) | 7.86(7.70) |
| 3f | White solid | 52 | 137—138 | 77.51(77.43) | 4.81(4.70) | 7.86(7.77) |
| 3g | White solid | 44 | 172—173 | 74.09(73.91) | 4.60(4.68) | 7.51(7.37) |
| 3h | White solid | 47 | 196—197 | 74.09(74.13) | 4.60(4.62) | 7.51(7.55) |
| 3i | White solid | 43 | 106—107 | 66.20(66.33) | 4.11(4.20) | 6.71(6.64) |
| 3j | White solid | 44 | 121—123 | 66.20(66.41) | 4.11(3.98) | 6.71(6.63) |
| 3k | White solid | 33 | 202—203 | 72.05(71.96) | 4.47(4.55) | 10.96(11.04) |
| Compd. | Appearance | Yield(%) | m. p./℃ | Elemental analysis(%), calcd.(found) | ||
| C | H | N | ||||
| 3l | White solid | 70 | 153—154 | 72.88(73.00) | 5.65(5.49) | 6.54(6.41) |
| 3m | White solid | 55 | 141—142 | 70.40(70.62) | 3.85(3.91) | 7.14(7.23) |
| 3n | White solid | 59 | 115—117 | 73.23(73.04) | 4.68(4.60) | 8.13(8.21) |
| 3o | White solid | 60 | 151—153 | 73.72(73.53) | 5.06(4.97) | 7.82(7.89) |
| 3p | White solid | 59 | 124—125 | 77.17(77.22) | 5.30(5.36) | 8.18(8.26) |
| 3q | White solid | 50 | 164—166 | 67.32(67.47) | 3.44(3.53) | 6.83(6.95) |
| 3r | White solid | 36 | 151—152 | 67.32(67.20) | 3.44(3.53) | 6.83(6.98) |
| 3s | White solid | 56 | 148—149 | 68.24(68.09) | 4.06(3.98) | 6.63(6.52) |
| Compd. | 1H NMR, δ(400 MHz, CDCl3) | 13C NMR, δ(101 MHz, CDCl3) |
|---|---|---|
| 3a | 8.10(d, J=7.8 Hz, 1H), 7.93(s, 1H), 7.66—7.61(m, 2H), 7.49—7.44(m, 1H), 7.42—7.24(m, 7H), 6.09(s, 1H), 5.56(s, 2H), 2.56(s, 3H) | 168.6, 162.6, 140.2, 138.3, 130.1, 129.3, 128.8, 128.5, 127.5, 126.8, 126.0, 123.4, 123.2, 120.6, 119.7, 108.5, 108.3, 100.2, 39.2, 21.4 |
| 3b | 8.13(d, J=7.8 Hz, 1H), 7.96(s, 1H), 7.52—7.49(m, 1H), 7.44(d, J=8.2 Hz, 1H), 7.38—7.23(m, 6H), 7.22—7.18(m, 1H), 6.06(s, 1H), 5.54(s, 2H), 2.60(s, 3H), 2.44(s, 3H) | 167.6, 163.3, 140.3, 138.4, 136.9, 131.1, 129.5, 129.3, 128.3, 127.5, 125.9, 123.6, 123.2, 120.6, 119.7, 108.6, 108.3, 102.9, 39.0, 21.5, 21.3 |
| 3c | 8.10(d, J=7.8 Hz, 1H), 7.93(s, 1H), 7.53(d, J=8.0 Hz, 2H), 7.48—7.44(m, 1H), 7.40(d, J=8.2 Hz, 1H), 7.34—7.24(m, 3H), 7.16(d, J=7.9 Hz, 2H), 6.06(s, 1H), 5.54(s, 2H), 2.56(s, 3H), 2.34(s, 3H) | 168.4, 162.6, 140.2, 138.3, 129.5, 129.3, 127.5, 126.7, 126.0, 125.6, 123.4, 123.1, 120.5, 119.7, 108.5, 108.3, 100.1, 39.2, 21.4 |
| 3d | 8.10(d, J=7.8 Hz, 1H), 7.93(s, 1H), 7.89—7.85(m, 1H), 7.50—7.42(m, 2H), 7.39—7.25(m, 4H), 7.18—7.15(m, 1H), 7.11—7.06(m, 1H), 6.37(d, J=3.3 Hz, 1H), 5.54(s, 2H), 2.56(s, 3H) | 168.4,161.4, 158.9, 158.1, 140.3, 138.3, 131.7(d, J=8.6 Hz), 129.3, 129.1(d, J=2.9 Hz), 127.5, 126.0, 124.6(d, J=3.5 Hz), 123.4, 123.2, 120.5(d, J=7.8 Hz), 119.7, 116.4, 116.2, 108.5, 108.3, 102.8(d, J=8.6 Hz), 38.9, 21.4 |
| 3e | 8.10(d, J=7.7 Hz, 1H), 7.93(s, 1H), 7.49—7.45(m, 1H), 7.40—7.35(m, 3H), 7.34—7.24(m, 4H), 7.09—7.04(m, 1H), 6.06(s, 1H), 5.53(s, 2H), 2.56(s, 3H) | 169.0, 164.1, 162.0, 161.4, 140.2, 138.2, 130.5(t, J=8.5 Hz), 129.4, 127.5, 126.1, 123.4, 123.2, 122.5(d, J=3.1 Hz), 120.6(d, J=7.2 Hz), 119.8, 117.1, 116.9, 113.9, 113.6, 108.5, 108.2, 100.2, 39.1, 21.4 |
| 3f | 8.10(d, J=7.1 Hz, 1H), 7.93(s, 1H), 7.63—7.59(m, 2H), 7.48—7.44(m, 1H), 7.39(d, J=8.1 Hz, 1H), 7.32—7.24(m, 3H), 7.06—7.00(m, 2H), 6.03(s, 1H), 5.54(s, 2H), 2.55(s, 3H) | 168.8, 165.0, 162.5, 161.7, 140.2, 138.2, 129.4, 128.7(d, J=8.6 Hz), 127.5, 126.1, 124.7(d, J=3.4 Hz), 123.4, 123.2, 120.6(d, J=7.3 Hz), 119.8, 116.1, 115.8, 108.5, 108.2, 100.1, 39.1, 21.4 |
| 3g | 8.11(d, J=7.8 Hz, 1H), 7.94(s, 1H), 7.61(dd, J=7.5, 2.0 Hz, 1H), 7.53—7.22(m, 8H), 6.40(s, 1H), 5.53(s, 2H), 2.58(s, 3H) | 167.8, 161.3, 140.3, 138.4, 132.8, 130.9, 130.4, 129.3, 127.9, 127.5, 127.1, 126.0, 123.4, 123.2, 120.6, 119.7, 108.6, 108.4, 103.7, 38.9, 21.5 |
| 3h | 8.11(d, J=7.8 Hz, 1H), 7.94(s, 1H), 7.65(s, 1H), 7.50—7.46(m, 2H), 7.39—7.22(m, 6H), 6.05(s, 1H), 5.49(s, 2H), 2.58(s, 3H) | 169.1, 161.5, 140.2, 138.2, 134.8, 130.3, 130.1, 129.4, 127.6, 126.8, 126.1, 124.9, 123.5, 123.2, 120.6, 119.8, 108.5, 108.2, 100.2, 38.9, 21.4 |
| 3i | 8.10(d, J=7.8 Hz, 1H), 7.93(s, 1H), 7.60(dd, J=8.0, 1.3 Hz, 1H), 7.53—7.42(m, 3H), 7.38—7.27(m, 4H), 7.26—7.20(m, 1H), 6.35(s, 1H), 5.54(s, 2H), 2.58(s, 3H) | 167.6, 162.6, 140.3, 138.3, 133.6, 130.0, 129.3, 127.5, 126.0, 123.4, 123.2, 122.2, 120.6, 119.7, 108.6, 108.4, 103.9, 38.9, 21.5 |
| 3j | 8.11(d, J=7.1 Hz, 1H), 7.93(s, 1H), 7.79(s, 1H), 7.55—7.53(m, 1H), 7.50—7.44(m, 2H), 7.38(d, J=8.2 Hz, 1H), 7.33—7.25(m, 3H), 7.19(t, J=7.9 Hz, 1H), 6.05(s, 1H), 5.52(s, 2H), 2.56(s, 3H) | 169.1, 161.4, 140.2, 138.2, 133.0, 130.5, 130.4, 129.7, 129.4, 127.5, 126.1, 125.3, 123.5, 123.2, 122.9, 120.6, 119.8, 108.4, 108.2, 100.1, 39.1, 21.4 |
| 3k* | 8.23(d, J=8.8 Hz, 2H), 8.08(d, J=7.7 Hz, 1H), 8.00(d, J=8.9 Hz, 2H), 7.92(s, 1H), 7.70(d, J=8.3 Hz, 1H), 7.61(d, J=8.4 Hz, 1H), 7.42(t, J=7.7 Hz, 1H), 7.27(d, J=7.8 Hz, 1H), 7.18(t, J=7.5 Hz, 1H), 7.04(s, 1H), 5.88(s, 2H), 2.43(s, 3H) | 170.6, 160.9, 148.8, 140.5, 138.6, 134.7, 128.9, 128.4, 127.7, 126.3, 124.7, 123.1, 122.8, 120.7, 119.8, 109.9, 109.7, 101.9, 38.4, 21.5 |
| Compd. | 1H NMR, δ(400 MHz, CDCl3) | 13C NMR, δ(101 MHz, CDCl3) |
| 3l | 7.97(d, J=7.8 Hz, 1H), 7.81(s, 1H), 7.35(t, J=7.7 Hz, 1H), 7.27(d, J=8.1 Hz, 1H), 7.22—7.10(m, 3H), 6.75(s, 2H), 5.95(s, 1H), 5.42(s, 2H), 3.74(s, 3H), 3.71(s, 6H), 2.43(s, 3H) | 167.7, 161.4, 152.4, 139.1, 138.6, 137.3, 128.3, 126.4, 124.9, 122.9, 122.3, 122.1, 119.5, 118.7, 107.4, 107.2, 102.9, 99.1, 59.8, 55.2, 38.2, 20.3 |
| 3m | 8.10(d, J=7.3 Hz, 1H), 7.93(s, 1H), 7.47(t, J=8.4 Hz, 1H), 7.38(d, J=8.1 Hz, 1H), 7.35—7.24(m, 4H), 7.21(d, J=3.7 Hz, 1H), 6.98(t, J=5.0 Hz, 1H), 6.00(s, 1H), 5.52(s, 2H), 2.56(s, 3H) | 168.6, 157.9, 140.2, 138.2, 130.2, 129.4, 127.9, 127.7, 127.5, 127.4, 126.4, 125.8, 123.4, 123.2, 120.8, 120.4, 119.8(d, J=17.7 Hz), 108.9, 107.9, 100.4, 100.1, 39.1, 21.4 |
| 3n | 8.10(d, J=7.7 Hz, 1H), 7.93(s, 1H), 7.47(t, J=8.4 Hz, 1H), 7.38(d, J=8.1 Hz, 1H), 7.35—7.24(m, 4H), 7.21(d, J=3.7 Hz, 1H), 6.98(t, J=5.0 Hz, 1H), 6.00(s, 1H), 5.52(s, 2H), 2.56(s, 3H) | 168.6, 157.9, 140.2, 138.2, 130.2, 129.4, 127.9, 127.7, 127.5, 127.4, 126.4, 125.8, 123.4, 123.2, 120.8, 120.4, 119.8, 108.9, 107.9, 100.4, 100.1, 39.1, 21.4 |
| 3o | 8.00(d, J=7.8 Hz, 1H), 7.83(s, 1H), 7.37(t, J=8.3 Hz, 1H), 7.29(d, J=8.2 Hz, 1H), 7.22—7.15(m, 3H), 6.91(d, J=3.5 Hz, 1H), 6.55(d, J=3.8 Hz, 1H), 5.86(s, 1H), 5.43(s, 2H), 2.46(s, 3H), 2.36(s, 3H) | 168.4, 158.0, 142.9, 140.2, 138.3, 129.4, 127.9, 127.7, 127.5, 126.1, 125.8, 123.5, 123.2, 120.6, 119.7, 108.5, 108.3, 99.9, 39.2, 21.4, 15.5 |
| 3p | 8.13(d, J=7.8 Hz, 1H), 7.96(s, 1H), 7.50(t, J=7.6 Hz, 1H), 7.40(d, J=8.2 Hz, 1H), 7.36—7.28(m, 3H), 6.65(d, J=3.3 Hz, 1H), 6.05(dd, J=3.4, 1.4 Hz, 1H), 6.00(s, 1H), 5.54(s, 2H), 2.59(s, 3H), 2.32(s, 3H) | 168.1, 155.0, 154.4, 142.0, 140.2, 138.3, 129.4, 127.5, 126.1, 123.5, 123.2, 120.6, 119.7, 111.9, 108.5, 108.3, 107.9, 99.6, 39.1, 21.5, 13.7 |
| 3q | 7.75(s, 1H), 7.66—7.59(m, 1H), 7.26—7.13(m, 5H), 7.13—7.05(m, 1H), 5.91(s, 1H), 5.44(s, 2H), 2.44(s, 3H) | 168.4, 159.2, 157.8, 155.5, 137.9, 135.3, 128.5, 127.2, 122.6(d, J=9.4 Hz), 121.9(d, J=3.8 Hz), 119.8, 112.8, 112.6, 110.4—109.9(m), 107.9(d, J=9.1 Hz), 107.3, 105.5, 105.2, 98.9, 38.1, 20.3 |
| 3r | 7.78—7.67(m, 2H), 7.23(s, 2H), 7.17(d, J=6.3 Hz, 2H), 7.04(q, J=5.3 Hz, 2H), 6.02(s, 1H), 5.62(s, 2H), 2.43(s, 3H) | 169.1, 159.1, 149.5, 147.1, 137.6, 129.0, 127.2, 126.3(d, J=8.8 Hz), 125.9(d, J=4.9 Hz), 122.4(d, J=2.1 Hz), 119.6, 118.9(d, J=6.5 Hz), 115.2(d, J=3.5 Hz), 111.1, 110.9, 110.2(d, J=6.5 Hz), 110.0(d, J=6.5 Hz), 107.5, 98.9, 39.7, 20.3 |
| 3s | 7.76(s, 1H), 7.45(s, 1H), 7.14—7.05(m, 5H), 6.97(dd, J=8.9, 4.0 Hz, 1H), 5.84(s, 1H), 5.36(s, 2H), 3.82(s, 3H), 2.43(s, 3H) | 168.7, 159.1, 153.1, 137.6, 133.9, 128.0, 126.5, 122.5, 122.2, 119.5, 113.9, 110.1(d, J=6.5 Hz), 109.9(d, J=6.5 Hz), 108.0, 107.1, 102.5, 98.8, 54.9, 38.0, 20.3 |
Table 2 1H NMR and 13C NMR data of compounds 3a—3s
| Compd. | 1H NMR, δ(400 MHz, CDCl3) | 13C NMR, δ(101 MHz, CDCl3) |
|---|---|---|
| 3a | 8.10(d, J=7.8 Hz, 1H), 7.93(s, 1H), 7.66—7.61(m, 2H), 7.49—7.44(m, 1H), 7.42—7.24(m, 7H), 6.09(s, 1H), 5.56(s, 2H), 2.56(s, 3H) | 168.6, 162.6, 140.2, 138.3, 130.1, 129.3, 128.8, 128.5, 127.5, 126.8, 126.0, 123.4, 123.2, 120.6, 119.7, 108.5, 108.3, 100.2, 39.2, 21.4 |
| 3b | 8.13(d, J=7.8 Hz, 1H), 7.96(s, 1H), 7.52—7.49(m, 1H), 7.44(d, J=8.2 Hz, 1H), 7.38—7.23(m, 6H), 7.22—7.18(m, 1H), 6.06(s, 1H), 5.54(s, 2H), 2.60(s, 3H), 2.44(s, 3H) | 167.6, 163.3, 140.3, 138.4, 136.9, 131.1, 129.5, 129.3, 128.3, 127.5, 125.9, 123.6, 123.2, 120.6, 119.7, 108.6, 108.3, 102.9, 39.0, 21.5, 21.3 |
| 3c | 8.10(d, J=7.8 Hz, 1H), 7.93(s, 1H), 7.53(d, J=8.0 Hz, 2H), 7.48—7.44(m, 1H), 7.40(d, J=8.2 Hz, 1H), 7.34—7.24(m, 3H), 7.16(d, J=7.9 Hz, 2H), 6.06(s, 1H), 5.54(s, 2H), 2.56(s, 3H), 2.34(s, 3H) | 168.4, 162.6, 140.2, 138.3, 129.5, 129.3, 127.5, 126.7, 126.0, 125.6, 123.4, 123.1, 120.5, 119.7, 108.5, 108.3, 100.1, 39.2, 21.4 |
| 3d | 8.10(d, J=7.8 Hz, 1H), 7.93(s, 1H), 7.89—7.85(m, 1H), 7.50—7.42(m, 2H), 7.39—7.25(m, 4H), 7.18—7.15(m, 1H), 7.11—7.06(m, 1H), 6.37(d, J=3.3 Hz, 1H), 5.54(s, 2H), 2.56(s, 3H) | 168.4,161.4, 158.9, 158.1, 140.3, 138.3, 131.7(d, J=8.6 Hz), 129.3, 129.1(d, J=2.9 Hz), 127.5, 126.0, 124.6(d, J=3.5 Hz), 123.4, 123.2, 120.5(d, J=7.8 Hz), 119.7, 116.4, 116.2, 108.5, 108.3, 102.8(d, J=8.6 Hz), 38.9, 21.4 |
| 3e | 8.10(d, J=7.7 Hz, 1H), 7.93(s, 1H), 7.49—7.45(m, 1H), 7.40—7.35(m, 3H), 7.34—7.24(m, 4H), 7.09—7.04(m, 1H), 6.06(s, 1H), 5.53(s, 2H), 2.56(s, 3H) | 169.0, 164.1, 162.0, 161.4, 140.2, 138.2, 130.5(t, J=8.5 Hz), 129.4, 127.5, 126.1, 123.4, 123.2, 122.5(d, J=3.1 Hz), 120.6(d, J=7.2 Hz), 119.8, 117.1, 116.9, 113.9, 113.6, 108.5, 108.2, 100.2, 39.1, 21.4 |
| 3f | 8.10(d, J=7.1 Hz, 1H), 7.93(s, 1H), 7.63—7.59(m, 2H), 7.48—7.44(m, 1H), 7.39(d, J=8.1 Hz, 1H), 7.32—7.24(m, 3H), 7.06—7.00(m, 2H), 6.03(s, 1H), 5.54(s, 2H), 2.55(s, 3H) | 168.8, 165.0, 162.5, 161.7, 140.2, 138.2, 129.4, 128.7(d, J=8.6 Hz), 127.5, 126.1, 124.7(d, J=3.4 Hz), 123.4, 123.2, 120.6(d, J=7.3 Hz), 119.8, 116.1, 115.8, 108.5, 108.2, 100.1, 39.1, 21.4 |
| 3g | 8.11(d, J=7.8 Hz, 1H), 7.94(s, 1H), 7.61(dd, J=7.5, 2.0 Hz, 1H), 7.53—7.22(m, 8H), 6.40(s, 1H), 5.53(s, 2H), 2.58(s, 3H) | 167.8, 161.3, 140.3, 138.4, 132.8, 130.9, 130.4, 129.3, 127.9, 127.5, 127.1, 126.0, 123.4, 123.2, 120.6, 119.7, 108.6, 108.4, 103.7, 38.9, 21.5 |
| 3h | 8.11(d, J=7.8 Hz, 1H), 7.94(s, 1H), 7.65(s, 1H), 7.50—7.46(m, 2H), 7.39—7.22(m, 6H), 6.05(s, 1H), 5.49(s, 2H), 2.58(s, 3H) | 169.1, 161.5, 140.2, 138.2, 134.8, 130.3, 130.1, 129.4, 127.6, 126.8, 126.1, 124.9, 123.5, 123.2, 120.6, 119.8, 108.5, 108.2, 100.2, 38.9, 21.4 |
| 3i | 8.10(d, J=7.8 Hz, 1H), 7.93(s, 1H), 7.60(dd, J=8.0, 1.3 Hz, 1H), 7.53—7.42(m, 3H), 7.38—7.27(m, 4H), 7.26—7.20(m, 1H), 6.35(s, 1H), 5.54(s, 2H), 2.58(s, 3H) | 167.6, 162.6, 140.3, 138.3, 133.6, 130.0, 129.3, 127.5, 126.0, 123.4, 123.2, 122.2, 120.6, 119.7, 108.6, 108.4, 103.9, 38.9, 21.5 |
| 3j | 8.11(d, J=7.1 Hz, 1H), 7.93(s, 1H), 7.79(s, 1H), 7.55—7.53(m, 1H), 7.50—7.44(m, 2H), 7.38(d, J=8.2 Hz, 1H), 7.33—7.25(m, 3H), 7.19(t, J=7.9 Hz, 1H), 6.05(s, 1H), 5.52(s, 2H), 2.56(s, 3H) | 169.1, 161.4, 140.2, 138.2, 133.0, 130.5, 130.4, 129.7, 129.4, 127.5, 126.1, 125.3, 123.5, 123.2, 122.9, 120.6, 119.8, 108.4, 108.2, 100.1, 39.1, 21.4 |
| 3k* | 8.23(d, J=8.8 Hz, 2H), 8.08(d, J=7.7 Hz, 1H), 8.00(d, J=8.9 Hz, 2H), 7.92(s, 1H), 7.70(d, J=8.3 Hz, 1H), 7.61(d, J=8.4 Hz, 1H), 7.42(t, J=7.7 Hz, 1H), 7.27(d, J=7.8 Hz, 1H), 7.18(t, J=7.5 Hz, 1H), 7.04(s, 1H), 5.88(s, 2H), 2.43(s, 3H) | 170.6, 160.9, 148.8, 140.5, 138.6, 134.7, 128.9, 128.4, 127.7, 126.3, 124.7, 123.1, 122.8, 120.7, 119.8, 109.9, 109.7, 101.9, 38.4, 21.5 |
| Compd. | 1H NMR, δ(400 MHz, CDCl3) | 13C NMR, δ(101 MHz, CDCl3) |
| 3l | 7.97(d, J=7.8 Hz, 1H), 7.81(s, 1H), 7.35(t, J=7.7 Hz, 1H), 7.27(d, J=8.1 Hz, 1H), 7.22—7.10(m, 3H), 6.75(s, 2H), 5.95(s, 1H), 5.42(s, 2H), 3.74(s, 3H), 3.71(s, 6H), 2.43(s, 3H) | 167.7, 161.4, 152.4, 139.1, 138.6, 137.3, 128.3, 126.4, 124.9, 122.9, 122.3, 122.1, 119.5, 118.7, 107.4, 107.2, 102.9, 99.1, 59.8, 55.2, 38.2, 20.3 |
| 3m | 8.10(d, J=7.3 Hz, 1H), 7.93(s, 1H), 7.47(t, J=8.4 Hz, 1H), 7.38(d, J=8.1 Hz, 1H), 7.35—7.24(m, 4H), 7.21(d, J=3.7 Hz, 1H), 6.98(t, J=5.0 Hz, 1H), 6.00(s, 1H), 5.52(s, 2H), 2.56(s, 3H) | 168.6, 157.9, 140.2, 138.2, 130.2, 129.4, 127.9, 127.7, 127.5, 127.4, 126.4, 125.8, 123.4, 123.2, 120.8, 120.4, 119.8(d, J=17.7 Hz), 108.9, 107.9, 100.4, 100.1, 39.1, 21.4 |
| 3n | 8.10(d, J=7.7 Hz, 1H), 7.93(s, 1H), 7.47(t, J=8.4 Hz, 1H), 7.38(d, J=8.1 Hz, 1H), 7.35—7.24(m, 4H), 7.21(d, J=3.7 Hz, 1H), 6.98(t, J=5.0 Hz, 1H), 6.00(s, 1H), 5.52(s, 2H), 2.56(s, 3H) | 168.6, 157.9, 140.2, 138.2, 130.2, 129.4, 127.9, 127.7, 127.5, 127.4, 126.4, 125.8, 123.4, 123.2, 120.8, 120.4, 119.8, 108.9, 107.9, 100.4, 100.1, 39.1, 21.4 |
| 3o | 8.00(d, J=7.8 Hz, 1H), 7.83(s, 1H), 7.37(t, J=8.3 Hz, 1H), 7.29(d, J=8.2 Hz, 1H), 7.22—7.15(m, 3H), 6.91(d, J=3.5 Hz, 1H), 6.55(d, J=3.8 Hz, 1H), 5.86(s, 1H), 5.43(s, 2H), 2.46(s, 3H), 2.36(s, 3H) | 168.4, 158.0, 142.9, 140.2, 138.3, 129.4, 127.9, 127.7, 127.5, 126.1, 125.8, 123.5, 123.2, 120.6, 119.7, 108.5, 108.3, 99.9, 39.2, 21.4, 15.5 |
| 3p | 8.13(d, J=7.8 Hz, 1H), 7.96(s, 1H), 7.50(t, J=7.6 Hz, 1H), 7.40(d, J=8.2 Hz, 1H), 7.36—7.28(m, 3H), 6.65(d, J=3.3 Hz, 1H), 6.05(dd, J=3.4, 1.4 Hz, 1H), 6.00(s, 1H), 5.54(s, 2H), 2.59(s, 3H), 2.32(s, 3H) | 168.1, 155.0, 154.4, 142.0, 140.2, 138.3, 129.4, 127.5, 126.1, 123.5, 123.2, 120.6, 119.7, 111.9, 108.5, 108.3, 107.9, 99.6, 39.1, 21.5, 13.7 |
| 3q | 7.75(s, 1H), 7.66—7.59(m, 1H), 7.26—7.13(m, 5H), 7.13—7.05(m, 1H), 5.91(s, 1H), 5.44(s, 2H), 2.44(s, 3H) | 168.4, 159.2, 157.8, 155.5, 137.9, 135.3, 128.5, 127.2, 122.6(d, J=9.4 Hz), 121.9(d, J=3.8 Hz), 119.8, 112.8, 112.6, 110.4—109.9(m), 107.9(d, J=9.1 Hz), 107.3, 105.5, 105.2, 98.9, 38.1, 20.3 |
| 3r | 7.78—7.67(m, 2H), 7.23(s, 2H), 7.17(d, J=6.3 Hz, 2H), 7.04(q, J=5.3 Hz, 2H), 6.02(s, 1H), 5.62(s, 2H), 2.43(s, 3H) | 169.1, 159.1, 149.5, 147.1, 137.6, 129.0, 127.2, 126.3(d, J=8.8 Hz), 125.9(d, J=4.9 Hz), 122.4(d, J=2.1 Hz), 119.6, 118.9(d, J=6.5 Hz), 115.2(d, J=3.5 Hz), 111.1, 110.9, 110.2(d, J=6.5 Hz), 110.0(d, J=6.5 Hz), 107.5, 98.9, 39.7, 20.3 |
| 3s | 7.76(s, 1H), 7.45(s, 1H), 7.14—7.05(m, 5H), 6.97(dd, J=8.9, 4.0 Hz, 1H), 5.84(s, 1H), 5.36(s, 2H), 3.82(s, 3H), 2.43(s, 3H) | 168.7, 159.1, 153.1, 137.6, 133.9, 128.0, 126.5, 122.5, 122.2, 119.5, 113.9, 110.1(d, J=6.5 Hz), 109.9(d, J=6.5 Hz), 108.0, 107.1, 102.5, 98.8, 54.9, 38.0, 20.3 |
| Reagent | Temp./℃ | Time/h | Solvent | Yield(%) | Reagent | Temp./℃ | Time/h | Solvent | Yield(%) |
|---|---|---|---|---|---|---|---|---|---|
| Et3N | 25 | 4 | DMF | 0 | Cs2CO3 | 25 | 8 | THF | 30 |
| K2CO3 | 25 | 4 | DMF | 0 | Cs2CO3 | 25 | 8 | CH2Cl2 | 16 |
| Cs2CO3 | 25 | 4 | DMF | 50 | K2CO3/KI | 25 | 8 | DMF | 0 |
| NaH | 25 | 4 | DMF | 18 | Cs2CO3/KI | 25 | 8 | DMF | 40 |
| Cs2CO3 | 25 | 6 | DMF | 59 | Cs2CO3 | 10 | 8 | DMF | 31 |
| Cs2CO3 | 25 | 8 | DMF | 63 | Cs2CO3 | 40 | 8 | DMF | 52 |
| Cs2CO3 | 25 | 10 | DMF | 58 | Cs2CO3 | 55 | 8 | DMF | 38 |
| Cs2CO3 | 25 | 8 | DMSO | 45 |
Table 3 Optimization of synthesis conditions of compound 3a
| Reagent | Temp./℃ | Time/h | Solvent | Yield(%) | Reagent | Temp./℃ | Time/h | Solvent | Yield(%) |
|---|---|---|---|---|---|---|---|---|---|
| Et3N | 25 | 4 | DMF | 0 | Cs2CO3 | 25 | 8 | THF | 30 |
| K2CO3 | 25 | 4 | DMF | 0 | Cs2CO3 | 25 | 8 | CH2Cl2 | 16 |
| Cs2CO3 | 25 | 4 | DMF | 50 | K2CO3/KI | 25 | 8 | DMF | 0 |
| NaH | 25 | 4 | DMF | 18 | Cs2CO3/KI | 25 | 8 | DMF | 40 |
| Cs2CO3 | 25 | 6 | DMF | 59 | Cs2CO3 | 10 | 8 | DMF | 31 |
| Cs2CO3 | 25 | 8 | DMF | 63 | Cs2CO3 | 40 | 8 | DMF | 52 |
| Cs2CO3 | 25 | 10 | DMF | 58 | Cs2CO3 | 55 | 8 | DMF | 38 |
| Cs2CO3 | 25 | 8 | DMSO | 45 |
| Compd. | R1 | R2 | MIC/(μg·mL-1) | |||
|---|---|---|---|---|---|---|
| S. aureus | S. epidermidis | E. coli | MRSA | |||
| 3a | Ph | H | 128 | >128 | >128 | >128 |
| 3b | 2⁃CH3Ph | H | >128 | >128 | 128 | >128 |
| 3c | 4⁃CH3Ph | H | 64 | 64 | >128 | 128 |
| 3d | 2⁃FPh | H | 128 | >128 | 64 | >128 |
| 3e | 3⁃FPh | H | 64 | 64 | >128 | 128 |
| 3f | 4⁃FPh | H | 16 | 32 | >128 | 32 |
| 3g | 2⁃ClPh | H | 128 | 128 | >128 | >128 |
| 3h | 3⁃ClPh | H | 128 | 128 | >128 | 128 |
| 3i | 2⁃BrPh | H | >128 | 128 | >128 | >128 |
| 3j | 3⁃BrPh | H | 128 | 128 | >128 | >128 |
| 3k | 4-NO2Ph | H | 8 | 8 | >128 | 16 |
| 3l | 3,4,5⁃Tri⁃OCH3Ph | H | 4 | 4 | 128 | 8 |
| 3m | 3,4,5⁃Tri⁃FPh | H | 2 | 2 | >128 | 4 |
| 3n | Thiophene⁃2⁃yl | H | >128 | >128 | 128 | >128 |
| 3o | 5⁃Methylthiophene⁃2⁃yl | H | >128 | >128 | 128 | >128 |
| 3p | 5⁃Methylfuran⁃2⁃yl | H | >128 | >128 | >128 | >128 |
| 3q | 3,4,5⁃Tri⁃FPh | 6⁃F | 0.5 | 1 | >128 | 2 |
| 3r | 3,4,5⁃Tri⁃FPh | 8⁃F | 16 | 16 | >128 | 32 |
| 3s | 3,4,5⁃Tri⁃FPh | 6⁃OCH3 | 4 | 4 | >128 | 8 |
| 3⁃Methylcarbazole | 64 | 128 | 64 | 128 | ||
| Oxacillin | 0.5 | 1 | 16 | >128 | ||
| Norfloxacin | 1 | 2 | 4 | 64 | ||
Table 4 MIC values of different target compounds
| Compd. | R1 | R2 | MIC/(μg·mL-1) | |||
|---|---|---|---|---|---|---|
| S. aureus | S. epidermidis | E. coli | MRSA | |||
| 3a | Ph | H | 128 | >128 | >128 | >128 |
| 3b | 2⁃CH3Ph | H | >128 | >128 | 128 | >128 |
| 3c | 4⁃CH3Ph | H | 64 | 64 | >128 | 128 |
| 3d | 2⁃FPh | H | 128 | >128 | 64 | >128 |
| 3e | 3⁃FPh | H | 64 | 64 | >128 | 128 |
| 3f | 4⁃FPh | H | 16 | 32 | >128 | 32 |
| 3g | 2⁃ClPh | H | 128 | 128 | >128 | >128 |
| 3h | 3⁃ClPh | H | 128 | 128 | >128 | 128 |
| 3i | 2⁃BrPh | H | >128 | 128 | >128 | >128 |
| 3j | 3⁃BrPh | H | 128 | 128 | >128 | >128 |
| 3k | 4-NO2Ph | H | 8 | 8 | >128 | 16 |
| 3l | 3,4,5⁃Tri⁃OCH3Ph | H | 4 | 4 | 128 | 8 |
| 3m | 3,4,5⁃Tri⁃FPh | H | 2 | 2 | >128 | 4 |
| 3n | Thiophene⁃2⁃yl | H | >128 | >128 | 128 | >128 |
| 3o | 5⁃Methylthiophene⁃2⁃yl | H | >128 | >128 | 128 | >128 |
| 3p | 5⁃Methylfuran⁃2⁃yl | H | >128 | >128 | >128 | >128 |
| 3q | 3,4,5⁃Tri⁃FPh | 6⁃F | 0.5 | 1 | >128 | 2 |
| 3r | 3,4,5⁃Tri⁃FPh | 8⁃F | 16 | 16 | >128 | 32 |
| 3s | 3,4,5⁃Tri⁃FPh | 6⁃OCH3 | 4 | 4 | >128 | 8 |
| 3⁃Methylcarbazole | 64 | 128 | 64 | 128 | ||
| Oxacillin | 0.5 | 1 | 16 | >128 | ||
| Norfloxacin | 1 | 2 | 4 | 64 | ||
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