Use of resveratrol-based perylene amide analogs in medicine
A technology based on peronamide and resveratrol, which is applied in the field of application of resveratrol-based peronamide analogs in the treatment of malignant tumors, and can solve the problem of unseen applications of resveratrol-based peronamide analogs And other issues
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Embodiment 1
[0017] Example 1: Compound BLBB-1 preparation of
[0018] The synthetic route is as follows:
[0019]
[0020] The synthetic route of intermediate 1 can be found in reference (Shoujiao Peng et al, J. Med. Chem. 2015,58, 5242−5255).
[0021] For the synthetic route of intermediate 2, please refer to the reference (Liu Wenhu et al., Acta Pharmaceutica Sinica, 2014, 49 (2): 217 −224).
[0022]
[0023] The synthetic route of intermediate 3 can be found in references (Hou Jian et al., China Journal of Pharmaceutical Industry, 2008, 39, 1, 1-8).
[0024] The synthetic route of compound BLBB-1 is shown in the literature (Hou Jian et al., China Journal of Pharmaceutical Industry, 2008, 39, 1, 1-8):
[0025]
[0026] Dissolve 10 mmol of intermediate 3 in 10 ml DMF under ice bath, add NaOCH 3 10 mmol and vigorously stirred, then 10 mmol of intermediate 2 was added dropwise, and reacted at room temperature for 10 h. Then it was poured into ice water, extracted with ethyl...
Embodiment 2
[0030] Example 2: Compound BLBB-2 preparation of
[0031] The synthetic route is as compound BLBB-1.
[0032] 1 H NMR (400 MHz, DMSO): δ9.50(s,1H), 9.14(s,1H), 7.92(d, J = 15.6 Hz,1H), 7.34 (d, J = 15.6 Hz,1H), 6.94 (d, J = 16.4 Hz, 1H), 6.92-6.90 (m, 3H), 6.82(d, J = 16.4 Hz, 1H), 6.52(d, J = 2.0 Hz, 2H), 6.21(t, J = 2.4 Hz, 1H), 6.01 (t, J = 9.6 Hz, 1H), 4.00 (t, J = 6.4 Hz, 2H), 3.88 (s, 6H), 2.44 (m, 2H).
[0033] MS-ESI (m / z): 421.15.
Embodiment 3
[0034] Example 3: Compound BLBB-3 preparation of
[0035] The synthetic route is as compound BLBB-1.
[0036] 1 H NMR (400 MHz, DMSO): δ9.52(s,1H), 9.12(s,1H), 7.90(d, J = 15.6 Hz,1H), 7.36 (d, J = 15.6 Hz,1H), 6.98 (d, J = 16.4 Hz, 1H), 6.94-6.92 (m, 3H), 6.80(d, J = 16.4 Hz, 1H), 6.54(d, J = 2.0 Hz, 2H), 6.22(t, J = 2.4 Hz, 1H), 6.03 (t, J = 9.6 Hz, 1H), 4.00 (t, J = 6.4 Hz, 2H), 2.42 (m, 2H).
[0037] MS-ESI (m / z): 397.11.
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