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. 2016 Nov 21;6(6):291–296. doi: 10.1007/s13659-016-0113-7

Table 1.

NMR data for compound 1 in DMSO-d 6. (600 MHz for 1H and 150 MHz for 13C)

Position δ H, mult. (J in Hz) δ C, mult. HMBC (1H–13C)
2 91.2, C
3 168.6, C
5 3.87, m
3.10, m
45.8, CH2 2, 6, 7
6 2.65, m
2.35, m
33.1, CH2 2, 5, 7, 8
7 79.0, C
8 130.1, C
9 6.56, d (7.7) 111.9, CH 8, 11
10 7.08, t (7.7) 129.8, CH 12, 13
11 6.81, t (7.7) 119.9, CH 9, 10
12 7.33, d (7.7) 123.2, CH 2, 10, 13
13 148.2, C
15 138.3, C
16 7.58, d (8.0) 123.3, CH 15, 17, 20, 21
17 7.74, t (8.0) 132.9, CH 15, 16, 19
18 7.43, t (8.0) 126.2, CH 15, 16, 20
19 7.72, d (8.0) 130.2, CH 15, 17, 21
20 127.9, C
21 164.3, C
N-Me 3.43, s 36.4, CH3 3, 15
N-H 6.00, s 2, 3, 7, 8, 13
7-OH 6.49, s 2, 7, 8