A kind of visible light catalytic method for synthesizing 6-sulfonemethylphenanthidine derivatives
A technology for sulfomephridine and derivatives, which is applied in the field of visible light catalytic synthesis of 6-sulfomephridine derivatives, can solve the problems of large functional group limitation, residual metal ions, serious environmental pollution and the like, and achieves the reaction time Short, low production cost, the effect of simplifying the process flow
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Embodiment 1
[0029]
[0030] At room temperature, add magneton, 2-(1-azidovinyl)-1,1'-biphenyl (0.26mmol, 57.5mg), p-toluenesulfonyl hydrazide (0.2mmol, 37.2mg ), Rose Bengal (0.004mmol, 4.07mg), TBPB (0.4mmol, 77.6mg) and Na 2 CO 3 (0.24mmol, 25.44mg), after changing the argon three times under vacuum, add 2ml of acetonitrile, react under 3W blue light irradiation for 10h, after the reaction is over, evaporate the solvent to obtain the crude product, then separate and purify by column chromatography to obtain the present embodiment 6- The product of sulfonemethylphenanthidine was 63.1 mg, the yield was 91%, and it was a pale yellow solid. 1 H NMR (400MHz, CDCl 3 )δ8.64(d,J=8.3Hz,1H),8.60–8.50(m,1H),8.36(d,J=8.2Hz,1H),7.84(ddd,J=9.8,6.0,4.9Hz,2H ),7.74(t,J=7.6Hz,1H),7.67(dd,J=6.2,3.4Hz,2H),7.56(d,J=8.2Hz,2H),7.18(d,J=8.0Hz,2H ),5.15(s,2H),2.38(s,3H). 13 C NMR (101MHz, CDCl 3 )δ149.76,144.61,143.25,135.54,133.78,133.16,133.10,130.85,129.86,129.39,128.64,127.59,127.58,126.98,125.56,...
Embodiment 2
[0032]
[0033] At room temperature, add magneton, 2-(1-azidovinyl)-4'-methyl-1,1'-biphenyl (0.26mmol, 61.1mg), p-toluenesulfonylhydrazide (0.2mmol, 37.2mg), Rose Bengal (0.004mmol, 4.07mg), TBPB (0.4mmol, 77.6mg) and Na 2 CO 3 (0.24mmol, 25.44mg), after changing the argon three times under vacuum, add 2ml of acetonitrile, react under 3W blue light irradiation for 10h, after the reaction is over, evaporate the solvent to obtain the crude product, then separate and purify by column chromatography to obtain the present embodiment 6- The product of sulfonemethylphenanthidine was 66.5 mg, the yield was 92%, and it was a pale yellow solid. 1 HNMR (400MHz, CDCl 3 )δ8.56(d, J=8.3Hz, 1H), 8.40(d, J=8.4Hz, 1H), 8.29(d, J=8.2Hz, 1H), 7.85–7.76(m, 1H), 7.71– 7.61(m,2H),7.56(d,J=8.3Hz,2H),7.47(dd,J=8.4,1.5Hz,1H),7.17(d,J=8.0Hz,1H),5.12(s,2H ),2.53(s,3H),2.37(s,3H). 13 C NMR (101MHz, CDCl 3 )δ149.65, 144.59, 143.45, 138.83, 135.67, 133.18, 130.76, 129.43, 129.38, 128.63, 127.10, 1...
Embodiment 3
[0035]
[0036] At room temperature, add magneton, 2-(1-azidovinyl)-4'-methoxy-1,1'-biphenyl (0.26mmol, 65.3mg), p-toluenesulfonyl Hydrazine (0.2mmol, 37.2mg), Rose Bengal (0.004mmol, 4.07mg), TBPB (0.4mmol, 77.6mg) and Na 2 CO 3 (0.24mmol, 25.44mg), after changing the argon three times under vacuum, add 2ml of acetonitrile, react under 3W blue light irradiation for 10h, after the reaction is over, evaporate the solvent to obtain the crude product, then separate and purify by column chromatography to obtain the present embodiment 6- The product of sulfonemethylphenanthidine was 65.6 mg, the yield was 87%, and it was a pale yellow solid. 1 HNMR(400MHz,DMSO)δ8.71(d,J=7.6Hz,1H),8.65(d,J=8.5Hz,1H),8.38(d,J=7.5Hz,1H),7.88(s,1H) ,7.64(d,J=6.9Hz,3H),7.35(d,J=6.9Hz,3H),7.26(s,1H),5.38(s,2H),3.90(s,3H),2.37(s, 3H). 13 C NMR(101MHz,DMSO)δ160.20,151.10,144.96,144.82,136.74,133.17,131.58,130.00,128.65,128.06,126.87,124.80,124.43,122.41,118.75,117.95,109.92,61.76,55.89,21.47.MS(ESI ...
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