id	author	title	date	pages	extension	mime	words	sentence	flesch	summary	cache	txt
eurjchem-492	Mikhaylichenko, Svetlana; Veloso, Anthony; Patel, Kunjal; Zaplishny, Vladimir	Synthesis and structure of new 1,2,3-triazolyl substituted 1,3,5-triazines	2012	9	.pdf	application/pdf	5870	233	69	; 1255.59 (m., ‐C‐N); 1196.13, 1137.17, 1088.66, 1007.09 (m., C‐O‐C) 8.03 (2H, s, NH2CO); 4.06 (3H, s, OCH3); 3.84 (4H, t, N‐ CH2, J= 5.0 Hz); 2.28 (3H, s, C‐CH3); 2.6 (3H, s, CH3); 1.59‐ 1.67 (6H, m, Σ 3CH2 in piperidyl) 318 (54) 3b 3379.29 (m, NH); 2923.19, 2852.61 (w., CH Ph); 1677.78 (st., C=O); 1598.02, 1570.00, 1497.41 (st. + m., C=C‐ + C=N conj.); 1239.09 (m., ‐C‐N); 1191.37, 1113.81, 1078.17, 1027.30 (m., C‐O‐C) 8.83 (1H, s, NH‐Ph); 7.71, 7.52, 7.27 (5H, m, CH in C6H5); 4.12 (3H, s, O‐CH3); 2.98 (3H, s, CCH3); 1.53‐1.63 (6H, m, Σ CH2 in piperidyl) 394 (71) 3c 3392.14 (m., NH); 2929.37, 2860.64 (w., CH Ph + Alk); 1663.12 (st., C=O); 1605.02, 1543.28, 1497.93 (st., + m., ‐C=C + ‐C=N conj.); 1255.35 (m., ‐C‐N); 1188.27, 1162.13, 1090.25, 1022.92 (m., C‐O‐C); 749.19 (w. Csp2–H o.o.p. bending, 1.2‐C6H4) 8.48 (1H, s, NH‐Ph); 7.28, 7.06, 6.93 (4H, m, CH in C6H4); 4.06 (6H, s, O‐CH3); 3.83 (4H, t, NCH2, J=8 Hz; 3.03 (3H, s, C‐CH3); 1.68 (6H, m, Σ 3CH2 in piperidyl) 424 (83) 3d 3380.74 (m., NH); 2928.87, 2857.73 (w., CH Alk); 1659.46 (st., C=O); 1600.18, 1538.44, 1501.02 (st. + m., ‐C=C + ‐C=N conj.); 1254.66 (m., ‐C‐N); 1149.93, 1103.89, 1088.94 1012.88 (m., C‐O‐C) 9.03 (2H, s, NH2CO); 3.82, (8H, t, Σ CH2N) J=7.6 Hz); 2.87 (3H, s, CCH3); 1.64 (12H m, Σ6 CH2 in piperidyl) 371 (90) 3e 3366.73 (m., NH); 2929.21, 2856.28 (w., CH Ph + Alk); 1657.03 (st., C=O); 1584.44, 1534.77, 1493.27 (st. + m., C=C‐ + C=N‐conj.); 1255.47 (‐C‐N); 1199.03, 1128.28, 1090.00, 1033.19 (C‐O‐C) 9.13 (1H, s, NHPh); 7.72, 7.35, 7.12 (5H, m, CH in C6H5); 3.80, (8H, t, Σ CH2N, J=4.0 Hz); 2.92 (3H, s, CCH3); 1.59 (12H m, Σ6 CH2 in piperidyl) 447 (55) 3f 3394.11 (m., NH); 2909.98, 2861.27 (w., CH Ph + Alk); 1664.98 (st., C=O); 1571.51, 1530.30, 1498.00 (st. + m., C=C‐ + C=N‐conj.); 1255.24 (‐C‐N); 1183.27, 1113.13, 1090.39, 1021.22 (C‐O‐C); 748.13 (w. Csp2–H o.o.p. bending, 1.2‐C6H4) 9.28 (1H, s, NH‐Ph); 7.32, 7.04, 6.91 (4H, m, CH in C6H4); 3.98 (3H, s, O‐CH3); 3.80 (8H, t, NCH2, J=6.3 Hz); 2.43 (3H, s, C‐CH3); 1.67 (12H, m, Σ6 CH2 in piperidyl) 477 (80) 3g 3312.76 (m., NH); 1678.59 (st., C=O); 1604.29, 1513.40, 1497.18 (st. + m., C=C‐ + C=N‐conj.); 1183.47, 1123.73, 1059.08, 1008.32 (C‐O‐ C) 7.68 (2H, s, CONH2); 3.93 (6H, s, OCH3); 2.51 (3H, s, C‐ CH3) 265 (93) 3h 3381.67 (m., NH); 2983.13, (w., CH Ph); 1687.24 (st., C=O); 1603.79, 1524.93, 1501.81 (st. + m., C=C‐ + C=N‐conj.); 1191.32, 1107.33, 1081.11, 1011.19 (C‐O‐C) 9.15 (1H, s, NHPh); 7.75 (2H, d, CH in C6H5, J=6.8 Hz); 7.43, 7.19 (3H, m, CH in C6H5); 2.83 (3H, s, OCH3); 2.06 (3H, s, CCH3) 341 (66) 3i 3312.76 (m., NH); 3074.07, 2932.79 (w., CH Ph + Alk); 1678.59 (st., C=O); 1606.29, 1513.40, 1495.87 (st. + m., C=C‐ + C=N‐conj.); 1183.47, 1123.73, 1085.08, 1008.32 (C‐O‐C); 717.31 (w. Csp2–H o.o.p. bending, 1.2‐C6H4) 8.28 (1H, s, NHPh); 7.50 (2H, d, CH in C6H4, J=7.9 Hz); 7.10, 6.95 (2H, m, CH in C6H4); 3.95 (9H, s, OCH3); 2.17 (3H, s, CCH3) 371 (55) 3j 3305.19 (m., NH); 3059.43 (w., CHPh); 1680.13 (st., C=O); 1596.77, 1564.76, 1497.00 (m., C=C‐ + C=N‐conj.); 1204.14, 1119.21, 1084.92, 1023.51 (C‐O‐C) 8.11 (2H, s, CONH2); 7.45 (4H, d, CH in C6H5, J=8.0 Hz); 7.21, 7.05 (6H, m, CH in C6H5); 2.18 (3H, s,CCH3) 389 (81) 3k 3375.98 (m., NH); 2934.53, (w., CH Ph); 1682.25 (st., C=O); 1600.38, 1516.38, 1496.56 (st. + m., C=C‐ + C=N‐conj.); 1190.05, 1169.13, 1061.68, 1013.09 (C‐O‐C) 8.36 (1H, s, PhNH); 7.36 (6H, d., CH in C6H5, J=6.6 Hz); 7.21, 7.05 (9H, m, CH in C6H5); 2.11 (3H, s,CCH3) 465 (43) 3l 3381.08 (m., NH); 3034.87, 2969.68 (w., CH Ph + Alk); 1679.71 (st., C=O); 1599.45, 1556.31, 1503.48 (st. + m., C=C‐ + C=N‐conj.); 1313.27 (‐C‐N) 9.18 (1H, s, NHPh); 7.78 (2H, d, CH in C6H5, J=7.2 Hz); 7.40, 7.15 (3H, m, CH in C6H5); 3.94 (1H, s, CH2NH); 3.80 (4H, q, CH2CH3, J=7.6 Hz); 2.76 (3H, s, C‐CH3); 1.35 (3H, t, CH2CH3, J=7.6 Hz) 367 (70) 3m 3358.27, 3289.60 (m., NH2CO); 1678.24 (st., C=O); 1596.35, 1568.18, 1499.36 (st. + m., C=C‐ + C=N‐, conj.); 1241.08 (m., ‐C‐N); 1196.32, 1107.68, 1069.58, 1004.08 (st. + m., C‐O‐C) 8.17 (2H, s, CONH2); 3.94 (8H, m, Σ4CH2O); 3.72 (8H, m, Σ 4CH2N); 2.19 (3H, s, CCH3) 375 (80) 3n 3375.51 (m., NH); 2977.25, 2899.16 (w., CH Ph + Alk); 1686.32 (st., C=O); 1599.14, 1553.19, 1501.03 (st. + m., C=C‐ + C=N‐, conj.); 1241.51 (m., C‐N); 1188.47, 1108.18, 1058.13, 1001.96 (st. + m., C‐ O‐C) 9.02 (1H, s, PhNH); 7.54 (2H, d, CH in C6H5, J=7.3 Hz); 7.36, 7.14 (8H, m, CH in C6H5); 3.90 (8H, m, Σ4 CH2O); 3.75 (8H, m, Σ 4 CH2N); 2.21 (3H, s, CCH3) 451 (44) 3o 3323.33 (m., NH); 2981.17, 2893.23 (w., CH Ph + Alk); 1681.83 (st., C=O); 1603.11, 1541.18, 1506.87 (m, ‐C=C + ‐C=N, conj.); 1250.18 (m, C‐N); 1177.09, 1107.08, 1063.24, 1001.22 (st. + m., C‐O‐C); 735.01 (m. Csp2–H o.o.p.	cache/eurjchem-492.pdf	txt/eurjchem-492.txt