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Saturday 6 September 2014

1,3-Dimethyl-3-(p-tolyl)-1H-pyrrolo[3,2-c]pyridin-2(3H)-one

Reaction scheme


1,3-Dimethyl-3-(p-tolyl)-1H-pyrrolo[3,2-c]pyridin-2(3H)-one

3: 1H NMR pdf(500 MHz, CDCl3)

δ: 1.80 (s, 3 H), 2.29 (s, 3 H), 3.21 (s, 3 H), 
6.88 (d, = 5.5 Hz, 1 H), 7.12 (d, = 8.0 Hz, 2 H), 7.21-7.19 (m, 2 H), 8.35 (s, 1 H), 8.52 (d, = 5.0 Hz, 1 H); 

13C NMR pdf(125 MHz, CDCl3) δ: 20.7, 23.7, 26.2, 50.3, 103.8, 126.1, 129.2, 130.1, 136.4, 137.2, 144.3, 149.7, 150.2, 179.0; 


IR (cast, cm-1): 3028, 2972, 2931, 1728, 1603, 1512, 1496, 1373, 1338, 1110, 1018, 818; 


HRMS (ESI): calcd. for C16H17N2O ([M+H]+): 253.1335, found: 253.1333; mp 103-104 °C; 

Anal. calcd. for C16H16N2O: C, 76.16; H, 6.39; N, 11.10, found: C, 76.09; H, 6.39; N, 11.11.








also

Analytical data for 2:

 1H NMR pdf(500 MHz, CDCl3) δ: 1.40 (d, = 7.0 Hz, 3 H), 2.30 (s, 3 H), 3.25 (s, 3 H), 3.71 (q, = 6.5 Hz, 1 H), 6.95 (d, = 7.5 Hz, 2 H), 7.00 (br d, = 5.4 Hz, 2 H), 7.05 (d, = 8.0 Hz, 2 H), 8.57-8.58 (m, 2 H); 

13C NMR pdf(125 MHz, CDCl3) δ: 20.4, 20.8, 36.9, 43.1, 121.5, 126.9, 129.2, 136.3, 138.0, 150.9, 151.0, 173.3; 

IR (cast, cm-1): 2975, 2930, 1668, 1587, 1513, 1496, 1375, 1274, 1126, 1063, 1024, 826; 

HRMS (ESI): calcd. for C16H192O ([M+H]+): 255.1492, found: 255.1488; mp 91-92 °C; 

Anal. calcd. for C16H18N2O: C, 75.56; H, 7.13; N, 11.01, found: C, 75.47; H, 7.21; N, 11.

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