有关有机合成的文献
No.11
陈悟等:含嗯二唑杂环取代的新型三唑并嘧啶衍生物的合成及其生物活性
‘1479
hkbkkkbbb
2-CH3-C6H4CH23-CH3一C6H4CH24-CH3一C6H4CH2
3-Cl—C6H4CH2
129~130114~115134~135127~128167~168114~115108~110141~142138~139107~10997~98135~137139~141162~16386~87168~169119~120
54.24(54.25)54.25(54.25)54.03(54.25)48.74(48.74)44.06(44.06)44.04(44.06)44.20(44.06)50.70(50.73)50.68(50.73)52.01(52.16)55.90(55.59)48.34(48.75)48.78(48.75)48.47(48.56)48.60(48.56)48.68(48.56)
4.47(4.55)4.46(4.55)4.42(4.55)3.45(3.61)3.14(3.26)3.17(3.26)3.16(3.26)3.69(3.76)3.68(3.76)4.27(4.38)4.31(4.42)3.74(3.86)3.75(3.86)3.27(3-36)
3.24(3.36)
21.3(21.09)21.23(21.09)21.23(21.09)20.16(20.06)18.25(18.14)18.24(18.14)18.33(18.14)21.12(20.88)21.04(20.88)20.36(20.27)20.74(20.47)22.12(22.11)22.21(22.11)20.20(19.99)20.15(19.99)20.17(19.99)17.54(17.46)
2一Br-C6出CH23一Br-C6地CH2
4-Br-C6H4CH22-F—C6H4CH24-RC6H4CH23-CH30_C6H4CH2
khkkkkkk
4一CH2=CH C鄙H2
2-N02-4-CH3一C6H3CH23一N02-4-CH3一C6H3CH2
3,5一F2一C6H3CH22,6—F2一C6H3CH22,4一F2-C6H3CH2
2一F一4-Br-C6H3CH2
3.30(3.36)2.85(2.93)
42.48(42.42)
表2化合物11~117的波谱数据
Table2
1HNMR锄dMS
spect脚da£aofcompoundsII~117
1HNMR(CDCl3,n讧S)d
Compd.
MS硪(%)
11
cz吼77;曩篙嚣'2盏盏’焉篙嚣,5嚣,焉譬鼍叠专嚣……’”熙0髦黑,“8。∞¨吲z4渤瑚5(18 1),67(12 1)
7:1j二j;.35孟,石,盈)”’
c25印瑚5c ㈣川焉意,嚣'3丢盖鬈’焉篙嚣,5嚣,嚣譬鬈‘:嚣鬻£.2罂,¨8。csq瑚s(21.7)'67(15 6)
12
焉与.丢蔷猛X蒜“”一“一…”一…”一~一“”
烈黑麓_鼎黧熙磐瑚Ⅲ渤,慧惫,嚣-:盏’焉篙嚣,5嚣,器sf潞盟蒜葛.丢蔷猫X菡~…一一一…“一…”一一一一”
107(12 1),105(100),77(19 2),67(13 5)
.
14
261(10.1),193(7.3),180(7.2),149(14.9),125(100),1082.64(s,3H,5-CH3),2.72(s,3H,7-CH3),4.38(s,2H,CH2Ph),
4.72(s,2H,SCH2),6.77(s,1H,6-H),7.23~7.40(m,4H,ArH)(65.7),107(35.5),67(39.8)
169(10.2),149(5.7),128(11.8),121(12.9),108(19.9),
107(21.7),77(85.5),67(17.2),44(100)
463(M+,0.1),261(12.7),193(9.7),169(29),149(17.5),108(100),107(61.8),89(88.7),67(51.4)
261(22.9),193(17.6),180(9.7),169(52.6),149(20.4),108(100),107(51.2),89(89.9),67(55.8)
26l(4.9),193(4.5),180(3.0),149(7.5),109(100),108(33.2),107(20.6),67(17.8)
261(1.9),193(1.5),109(100),108(24.8),107(13.8),67
(14.2)
.
2.64(s,3H,5一CH3),2.72(s,3H,7一CH3),4.53(s,2H,CH2P峋,4.72(s,2H,SCH2),6.77(s,1H,6一H),7.12~7.58(m,4H,ArH)2.64(s,3H,5一CH3),2.72(s,3H,7一CH3),4.37(s,2H,CH2Ph),4.71(s,2H,SCH2),6.77(s,1H,6一H),7.15~7.55(m,4H,√蛀H)2.64(s,3H,5-CH3),2.71(s,3H,7一CH3),4.35(s,2H,CH2Ph),4.71(s,2H,SCH2),6.77(s,1H,6一H),7.26~7.43(m,4H,ArH)2.64(s,3H,5-CH3),2.72(s,3H,7-CH3),4.44(s,2H,CH2Ph),4.72(s,2H,SCH2),6.76(s,1
”
。16
.
1
。
ls
H,6-H),7.01~7.48(m,4H,棚)
.
2.66(s,3H,5一CH3),2.74(s,3H,7一CH3),4.40(s,2H,CH2Ph)’4.72(s,2H,SCH2),6.77(s,1H,6-H),7.12~7.28(m,4H,ArH)
19