2多氟烷基取代和葡萄糖基取代的24二氢124三唑3硫酮类席夫碱的合成及其杀虫活性(7)

雅有古意 分享 2021-06-02 下载文档

C25H15F17N4S:C41.33,H2.08,N7.7l:foundC41.21,H2.17,N7.79.

5c:白色固体,产率85%,111.P.85~87℃;1H卜MR

(CDCl3,400MHz)J:2.72~2.85(ITI,2H,CH2CH2C6F13),3.49"--3.53(m,2H,CH2C6F13),7.45~7.48(m,3H,c6H5),Hz,2H,C6H4),7.76(d,J=8.4Hz,2H,186,

1142

cm-1;MSm/z:660.8([M+1】十).Anal.calcdfor

41.80,H2.14,N8.48;foundC41.69,2.23.N8.59.

5d:白色固体,产率86%,m.P.109~111℃;1H

MHz)6:2.74~2.83(m,2H,

Hz,2H,C6H4),7.76Hz,2H,C6H4),7.86~7.87(in,2H,C6H5),8.39

MHz)J:--80.35

一122.36(s,2F),一122.88(s,2F),一125.75(m,2F);IR(KBr)1,:3037,1597,1452,1358,1252,1219,115lcm一1;m/z:760.7([M+1】十).Anal.calcdforC25H14C1F17N4S:

39.46。H1.85,N7.36;foundC39.61,H1.77,N7.19.

5e:白色固体,产率81%,n1.P.157~159℃;1HMHz)万:2.71~2.84“n,2H,

Hz,1H,C6H5),7.20(dd,,2

1.6,8.4Hz,1H,C6I-13),7.45(d,J=7.2Hz,2H,C6H3),7.50

(d'-,=1.6Hz,2H,C6H5),7.88~7.90(m,2H,C6H5),8.29(s,IH,CH=N);IR(KBr)’,:3076,1598,1515,1472,

1430,1372,1304,1251,1214,1149cm-1;MSm/z:672.8

(【M+1】十).Anal.calcdforC24Hi7F13N402S:C42.87,H

2.55,N8.33;foundC42.91,H2.51,N8.31.

5f.白色固体,产率83%,in.P.169~17l℃;1H

NMR(CDCl3,400MHz,)巧:2.70~2.83(m,2H,CH2CH2C8F17),3.46~3.50(m,2H,CH2CsFl7),3.99(s,3H,OCH3),7.03(d,J=8.0Hz,lH,C6H5),7.20(dd,.,=

1.6,8.4Hz,1H,C6H3),7.45(d,J----7.2Hz,2H,C6H3),7.50

(d,.,=1.6Hz,2H,C6H5),7.88---7.90(In,2H,C6H5),8.28(s,1H,CH=N);”FNMR(CDCl3,376MHz)J:--80.36(m,3F),一113.89(m,2F),一121.34~一121.57(m,6F),~122.37(s,2F),一122.88(s,2F),一125.76(m,2F);IR(KBr)¨3078,1595,1516,1468,1431,1371,1302,1252,

1213,1149cml;MS

m/z:772.8([M+1】十).Anal.calcd

forC26H17F17N402S:C40.43,H2.22,N7.25;foundC

2.31,N7.21.

59:白色固体,产率91%,111.P.176--一178℃;1H

NMR(CDCl3,400

MHz)J:2.77~2.90(m,2H,

CH2CH2C6F13),3.42--。3.46(nl,2H,CH2C6F13),6.93(d,

J=8.4Hz,2H,C6H4),7.49~7.51(m,3H,C6H5),7.76(d,Hz,2H,C6r14),7.82~7.85(m,2H,C6Hd,8.69(s,

1H,CH=N),10.56(s,1H,OH);IR(KBr)',:3062,1593,

1520,1456,1361,1302,1255,1169,1140cm-1;MSm/z:

642.7(【M+1】十).Anal.calcdforC23H15F13N40S:C

43.00,

H2.35.N8.72;foundC43.16,H2.31,N8.57.

5h:白色固体,产率90%,in.P.185~187℃;1H

NMR(CDCl3,400

MHz)6:2.73~2.82(m,2H,

CH2CH2C8F17),3.43~3.47(m,2H,CH2CsFl7),6.94(d,

Hz,2H,C6}14),7.49~7.52(m,3H,C6H5),7.76(d,Hz,2H,C6H4),7.83~7.86(m,2H,C6H5),8.69(s,

1H,CH=N),lO.55(s,1H,0H);19FNMR(CDCl3,376一121.56(m,6F),一122.37(s,2F),一122.89(s,2F),一125.75(m,2F);IR(KBr)’,:3058,1587,1520,1456,

1363,1296,1225,l147cm-1;Ms

m/z:742.8([M+l】十).Anal.calcdforC25H15F17N40S:C

40.44,H2.04,N

7.55;

foundC40.28。H2.21。N7.59.

5i:白色固体,产率89%,n1.P.166

168℃;1H

NMR(DMSO一,/6,400MHz)J:2.78~2.92(1珥2H,CHzCHzC6Fjs),3.44""3.48(m,2H,CH2Q,13),6.94~(iil,3H,C6H5),8.95(s,1H,CH=N),10.56(s,1H,OH);IR(KBr)v:3035,1608,1462,1356,1230,l194,1144

2多氟烷基取代和葡萄糖基取代的24二氢124三唑3硫酮类席夫碱的合成及其杀虫活性(7).doc 将本文的Word文档下载到电脑

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