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. 2015 Feb 11;33(2):244–259. doi: 10.1007/s11419-015-0268-7

Table 4.

NMR data of compound 4 and NNEI indazole analog

No. NNEI 1H-indazole analoga Compound 4 b
13C 13C 1H
1 160.9 159.0
2′
3′ 137.3 127.1
3′a 123.0 120.6
4′ 122.9 118.2 7.94, 1H, d, J = 9.6 Hz, overlapped
5′ 122.9 124.9 7.34, 1H, td, J = 7.6, 0.7 Hz
6′ 126.9 126.3 7.40, 1H, ddd, J = 7.6, 6.5, 1.0 Hz
7′ 109.4 119.0 7.88, 1H, d, J = 8.9 Hz
7′a 141.1 147.3
1″ 49.6 53.4 4.89, 2H, t, J = 7.2 Hz
2″ 29.5 31.0 2.04, 2H, m
3″ 29.0 28.9 1.35, 2H, m, overlapped
4″ 22.3 22.3 1.35, 2H, m, overlapped
5″ 14.0 14.0 0.87, 3H, t, J = 7.2 Hz
1″′ 132.4 131.8
2″′ 119.4 121.1 8.08, 1H, d, J = 7.6 Hz
3″′ 126.0 126.2 7.55, 1H, m, overlapped
4″′ 125.0 126.6 7.79, 1H, d, J = 8.3 Hz
4″′a 134.2 134.3
5″′ 128.8 129.0 7.93, 1H, m, overlapped
6″′ 125.9 126.8 7.54, 1H, m, overlapped
7″′ 126.2 125.8 7.57, 1H, m, overlapped
8″′ 120.5 120.4 7.92, 1H, m, overlapped
8″′a 126.7 127.2
NH 8.25, 1H, brs

aRecorded in CDCl3 at 800 MHz (1H) and 200 MHz (13C), respectively; data in δ ppm (J in Hz)

bRecorded in CDCl3 at 600 MHz (1H) and 150 MHz (13C), respectively; data in δ ppm (J in Hz)