Chapter – 2 Microwave assisted simple and fast….. for C16H22N2O: C, 74.38; H, 8.58; N, 10.84. Found: C, 74.34; H, 8.54; N, 10.80. 2-METHYL-1-(2-MORPHOLIN-4-YL-2-OXO ETHYL) INDOLINE (DNJ-402): IR (KBr, cm -1 ): 3110 (Ar-H), 2949 (–CH3), 2855 (–CH2), 1735 (>CO), 1613, 1469, 1439 (Ar-H), 1113 (C-N, Aliphatic, 3°), 1050 (C-O-C); 1 H NMR (400 MHz, CDCl3): δ (ppm) 1.28 (3H, m), 2.45 (4H, t), 2.62 (1H, s), 2.83 (1H, s), 3.14 (1H, s), 3.73 (4H, t), 4.44 (2H, s), 6.63 (2H, m), 7.00 (2H, m); MS m/z = 260 (M + ); Anal. Calcd. for C15H20N2O2: C, 69.20; H, 7.74; N, 10.76. Found: C, 69.24; H, 7.70; N, 10.80. 2-METHYL-1-[2-(4-METHYL PIPERAZIN-1-YL)-2-OXO ETHYL] INDOLINE (DNJ-403): IR (KBr, cm -1 ): 3082 (Ar-H), 2964 (–CH3), 2859 (–CH2), 1730 (>CO), 1627, 1534, 1480, 1423 (Ar-H), 1120 (C-N, Aliphatic, 3°); MS m/z = 273 (M + ); Anal. Calcd. for C16H23N3O: C, 70.30; H, 8.48; N, 15.37. Found: C, 70.26; H, 8.46; N, 15.40. 1-[2-(4-ETHYL PIPERAZIN-1-YL)-2-OXO ETHYL]-2-METHYL INDOLINE (DNJ-404): IR (KBr, cm -1 ): 3105 (Ar-H), 2969 (–CH3), 2848 (–CH2), 1722 (>CO), 1662, 1500, 1447 (Ar-H), 1110 (C-N, Aliphatic, 3°); MS m/z = 287 (M + ); Anal. Calcd. for C17H25N3O: C, 71.04; H, 8.77; N, 14.62. Found: C, 71.08; H, 8.80; N, 14.65. 1-[2-(4-BENZYL PIPERAZIN-1-YL)-2-OXO ETHYL]-2-METHYL INDOLINE (DNJ-405): IR (KBr, cm -1 ): 3068 (Ar-H), 2963 (–CH3), 2865 (–CH2), 1730 (>CO), 1620, 1470, 1445 (Ar-H), 1130 (C-N, Aliphatic, 3°); MS m/z = 349 (M + ); Anal. Calcd. for C22H27N3O: C, 75.61; H, 7.79; N, 12.02. Found: C, 75.57; H, 7.82; N, 12.05. 1-(3-PIPERIDIN-1-YL PROPYL)-1H-INDOLE-2, 3-DIONE (DNJ-501): IR (KBr, cm -1 ): 3100 (Ar-H), 2963 (–CH3), 2846 (–CH2), 1724 (>CO, C12), 1680 (>CO, C11), 1610, 1555, 1448 (Ar-H), 1120 (C-N, Aliphatic, 3°); MS m/z = 272 (M + ); Anal. Calcd. for C16H20N2O2: C, 70.56; H, 7.40; N, 10.29. Found: C, 70.60; H, 7.42; N, 10.32. Department of Chemistry, <strong>Saurashtra</strong> <strong>University</strong>, Rajkot – 360 005 99
Chapter – 2 Microwave assisted simple and fast….. 1-(3-MORPHOLIN-4-YL PROPYL)-1H-INDOLE-2, 3-DIONE (DNJ-502): IR (KBr, cm -1 ): 3137 (Ar-H), 2953 (–CH3), 2863 (–CH2), 1730 (>CO, C12), 1682 (>CO, C11), 1609, 1562, 1461 (Ar-H), 1118 (C-N, Aliphatic, 3°), 1050 (C-O-C); 1 H NMR (400 MHz, CDCl3): δ (ppm) 1.28 (2H, m), 2.83 (6H, m), 3.73 (2H, t), 4.52 (4H, t), 6.63 (2H, m), 7.00 (2H, m); MS m/z = 274 (M + ); Anal. Calcd. for C15H18N2O3: C, 65.68; H, 6.61; N, 10.21. Found: C, 65.70; H, 6.64; N, 10.24. 1-[3-(4-METHYL PIPERAZIN-1-YL) PROPYL]-1H-INDOLE-2, 3-DIONE (DNJ-503): IR (KBr, cm -1 ): 3090 (Ar-H), 2969 (–CH3), 2855 (–CH2), 1721 (>CO, C12), 1683 (>CO, C11), 1600, 1550, 1433 (Ar-H), 1127 (C-N, Aliphatic, 3°); MS m/z = 287 (M + ); Anal. Calcd. for C16H21N3O2: C, 66.88; H, 7.37; N, 14.62. Found: C, 66.90; H, 7.40; N, 14.65. 1-[3-(4-ETHYL PIPERAZIN-1-YL) PROPYL]-1H-INDOLE-2, 3-DIONE (DNJ- 504): IR (KBr, cm -1 ): 3081 (Ar-H), 2950 (–CH3), 2861 (–CH2), 1729 (>CO, C12), 1685 (>CO, C11), 1627, 1544, 1433 (Ar-H), 1115 (C-N, Aliphatic, 3°); MS m/z = 301 (M + ); Anal. Calcd. for C17H23N3O2: C, 67.75; H, 7.69; N, 13.94. Found: C, 67.71; H, 7.66; N, 13.91. 1-[3-(4-BENZYL PIPERAZIN-1-YL) PROPYL]-1H-INDOLE-2, 3-DIONE (DNJ-505): IR (KBr, cm -1 ): 3075 (Ar-H), 2960 (–CH3), 2840 (–CH2), 1730 (>CO, C12), 1688 (>CO, C11), 1624, 1575, 1525, 1440 (Ar-H), 1122 (C-N, Aliphatic, 3°); MS m/z = 363 (M + ); Anal. Calcd. for C22H25N3O2: C, 72.70; H, 6.93; N, 11.56. Found: C, 72.68; H, 6.95; N, 11.60. 1-(PIPERIDIN-1-YL ACETYL)-1H-INDOLE-2, 3-DIONE (DNJ-601): IR (KBr, cm -1 ): 3080 (Ar-H), 2963 (–CH3), 2854 (–CH2), 1723 (>CO, C12), 1687 (>CO, C11), 1663 (>CO, C7), 1615, 1519, 1450 (Ar-H), 1125 (C-N, Aliphatic, 3°); MS m/z = 272 (M + ); Anal. Calcd. for C15H16N2O3: C, 66.16; H, 5.92; N, 10.29. Found: C, 66.20; H, 5.89; N, 10.31. 1-(MORPHOLIN-4-YL ACETYL)-1H-INDOLE-2, 3-DIONE (DNJ-602): IR (KBr, cm -1 ): 3069 (Ar-H), 2953 (–CH3), 2864 (–CH2), 1713 (>CO, C12), 1682 (>CO, C11), 1659 (>CO, C7), 1609, 1519, 1454 (Ar-H), 1117 (C-N, Aliphatic, Department of Chemistry, <strong>Saurashtra</strong> <strong>University</strong>, Rajkot – 360 005 100
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Saurashtra University Re - Accredit
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Statement under O. Ph. D. 7 of Saur
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ACKNOWLEDGEMENT It is a moment of g
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Jignesh Lunagariya, Hitesh Sarvaiya
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CONTENT Content General Remarks 6 A
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Content 3.2 Reaction scheme 149 3.3
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MF Molecular Formula MW Molecular W
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GABA Gamma Amino Butyric Acid MES M
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Conferences / Seminar / Workshop At