Compound M.P.
(oC) Yield (%) FT-IR (cm-1)vmax / 1HNMR , C13NMR (500 MHz, CDCl3)/ MS (EI) (m/z)
1750 (C=O), 1323(C-N), / 3.91( 2H, OCCH2), 6.76 (1H, quinoline, Ar-H), 7.18 (3H, Ar-
5a 576.75 85 H), 7.29-7.37, ( 3H, Ar-H), 7.47 (1H, Pyridine), 7.82 (1H, quinolone), 8.74 (1H,pyridine)
8.89 (1H, pyridine)/ 35.5, 87.5,120, 124, 128.9, 134, 135, 154, 156.1,171
1650 (C=O), 3400 (N-H)/ 0.89 (6H, (CH3)2, 1.30 (4H, (CH2)2, 2.13 (2H, CH2), 3.73(2H,
5b 273.23 80 H-Ar), 5.92(1H, H-Ar), 6.82(1H, H-Ar), 6.92 (1H, N-H), 7.02 (1H, H-Ar)/ 0.89, 19.9,
34.8, 43.7, 124.01, 125.5, 135.2, 142.9, 154.9, 156.1, 76.9
1725 (C=O), 1250 (C-O), 808 (C-N),/ 1.64 (3H CH3), 3.71 (1H H-Ar), 3.81 ( 3H CH3),
5c 465.24 65 7.06 (1H H-Ar), 7.23 (1H H-Ar), 7.34 ( 1H H-Ar), 7.48-7.49 (2H, H-Ar), 7.73-7.82 (3H,
quinoline), 8.74 (1H, H-Ar), 8.89 (1H, N-H)/ 13.7, 40.4, 55.8, 87.5, 105.4, 124, 126.7,
128.5, 132.5, 133.5, 134.9, 135.2, 154.9, 156.1, 170.0
5d 363.82 80 1650 (C=O), 808 (C-N),/ 7.43-7.45 (2H H-Ar), 7.65-7.73 (3H, H-Ar), 8.12 (1H, H-Ar),
8.83 (1H, H-Ar), 8.97 (1H, N-H)/ 78.2, 124.1, 126.7, 130, 131.7, 131.8, 133.9, 134, 135.4,
140.5,154.8, 161, 165.2
5e 412.57 78 1675 (C=O), 808 (C-N),/ 4.14 (2H, COCH2), 7.47 (1H, H-Ar), 7.61-7.79 (5H, H-Ar),
8.85(1H, H-Ar), 8.96 (1H, N-H)/ 78.2 121.4, 124.1, 125.7, 126.7, 127.6, 130, 131.8, 133,
134, 135.4, 140.5,154.8, 161, 165.2
1735 (C=O), 1250 (C-O), 808 (C-N), 700 ( C-Cl)/ 2.30 (S, 3H, H-CH3), 2.48 (S, 3H, Me),
5f 368.96 75 7.22 – 7.27 ( D, 2H ,H-Ar), 7.65-7.69 ( D, 2H, H-quinoline), 8.08 ( D, 1H, H-Ar), 8.83 (D,
1H, H-Ar), 8.97 ( D, 1H, C-N, quinoline)/ 21.6, 21.7 78.2, 124.1, 125.7, 128.7, 130.8,
134.0, 134,135.4, 139.8, 140.5, 143, 154, 161, 165.2
1740 (C=O), 1250 (C-O), 808 (C-N), 1100( C-Fl)/ 1.07 ( m, 1H, N-H), 1.33 ( m, 4H,
5g 778.9 70 (CH2)2), 2.78 (t, 4H, (CH2 )2), 3.46 (t, 2H, CH2), 4.12 (q, 1H, cyclopropane ), 6.01 (d, 1H,
H-Ar), 7.65-7.69 (q, 2H, H-Ar), 8.01 (d, 1H, H-Ar), 8.09 (s, 1H, H-Ar), 8.83 (d, 1H, H-
Ar), 8.97 (d, 1H, C-N)/ 7.7, 35.8, 45.8, 51.3, 78.2, 102.5, 109.3, 112.2, 124.1, 125.7,
130.5, 134, 135.4, 136.8, 140.5, 146.9, 152.5, 154.8, 161,162, 176.4
1735 (C=O), 1250 (C-O), 808 (C-N)/ 7.22 ( d, 1H, H-Ar), 7.57-7.60 (m, 2H, H-Ar),
5h 367 85 7.65-7.69 ( m, 2H, quinoline), 8.25 (d, 1H, H-Ar), 8.83 ( d, 1H, H-Ar), 8. 97 (d, 1H, H-
Ar)/ 55.8, 78.2, 114.2, 120.9, 124.1, 125.7,130, 131.3, 134,134.9, 140.5, 154.8, 158.5,
161, 169.1
1735, 1750 (C=O), 1250 (C-O), 808 (C-N)/ 1.9 ( d, 3H, Me), 2.21 (s, 3H, Me), 2.35 ( t,
5i 520.9 80 4H H-Ar), 3.23 ( t, 2H, CH2), 3.44 (s, 4H, H-Ar), 3.99-4.24 ( t, 2H, H2C-O), 7.69 (d, 1H,
H-Ar) 8.66 (s, 1H,H-Ar), 14.93 ( t, 1H, OH)/ 17.9, 46.6, 57.2, 59.4, 65.9, 71.1, 103.8,
109.3, 123.4, 126, 132.6, 143.1, 146.9, 158.2, 166.2, 170.4
1635 (C=O), 1250 (C-O)2, 808 (C-N)/ 3. 84- 3.90 ( s, 6H, (OCH3)2), 5.70 ( s, 2H, CH2),
5j 454.5 70 6.72-6.75 (d, 2H, H-Ar), 7.60, 7.62, 7.65 ( m, 3H, H-Ar), 8.70 ( d, 1H, H-Ar), 8.85 ( d,
1H, HC-N)/ 55.8, 73.1, 74.1, 96.8, 106.5, 112.5, 123.9, 129.5, 130.8, 133.7, 135.3, 141.7,
153.6, 162.2, 164,168, 198.3
1650 (C=O), 1250 (C-O), 808 (C-N)/ 3.32 (s, 3H, CH3), 7.65, 7.69 ( t, 2H, H-Ar), 8.83
5k 450 75 (d, 1H, quinoline) 8.97 ( d, 1H, H-Ar) 9.24 ( s, 1H, imidazole) 13.0 (d, 1H, N-H,
imidazole)/ 30.7,78.2, 124.7, 129, 130, 134, 135.4, 140.5,149, 150.8,154.8, 161, 162.8
1700 (C=O), 1200 (C-O), 808 (C-N)/1.18 ( t, 1H, 3H, CH3), 2.71 ( q, 2H, CH2), 5.70 ( s,
5l 397.5 80 2H, OCH2), 7.33 ( q, 1H, H-Ar), 7.60- 7.62 ( t, 3H, H-Ar), 7.80 ( d, 2H, H-Ar), 7.96 ( q,
1H, H-Ar), 8.70 ( d, 1H, H-Ar), 8.85 ( d, 1H, H-Ar)/ 74.1, 27.3, 73.1, 74.1, 123.9,
124.5,127.5, 127.6,129.4, 133, 133.7, 135.5, 135.7,141.7, 143.5, 153.6, 164.8, 198.3