A kind of naphthoquinone compound against novel coronavirus and its medical use
A technology of coronaviruses and compounds, applied in the field of medicine, achieves the effect of strong inhibitory activity, simple preparation method, and good prospects for new drug development
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Embodiment 1
[0024] This embodiment relates to a preparation method of 5-hydroxy-1,4-naphthoquinone (II-1) having structural formula (II), comprising the following steps:
[0025]
[0026] Add 75mL 30% H to a 250mL three-necked bottle 2 o 2 , stirred and added dropwise 42mL of acetic anhydride, and kept the temperature of the reaction solution not exceeding 40°C during the dropwise addition. After dropping, stir at 40°C for 4 hours. Afterwards, 100 mL methanol solution of 1,5-dihydroxynaphthalene (15 g, 93.7 mmol) was added dropwise to the reaction solution under vigorous stirring, and the rate of addition was controlled so that the temperature of the reaction solution did not exceed 60°C. Continue to stir for 1 hour after the dropwise addition, pour into ice water after cooling, a large amount of tan precipitate precipitates, filter and dry to obtain a dark red solid powder. Purification was carried out by silica gel column chromatography (mobile phase: ethyl acetate-petroleum ether...
Embodiment 2
[0028] This embodiment relates to a preparation method of 5-methoxy-1,4-naphthoquinone (juglone methyl ether) (II-2) having structural formula (II), comprising the following steps:
[0029]
[0030] Compound II-1 (3g, 17.2mmol) described in Example 1 was dissolved in 90mL of THF-H 2 To the O (2:1) mixed solution, tetrabutylammonium bromide (1.6g, 5.2mmol), hydrosulfite (11.2g, 64.3mmol) and sodium hydroxide (9.6g, 240mmol) were sequentially added under stirring. Gabby, in N 2Under protection, dimethyl sulfate (10 mL, 103 mmol) was added dropwise. After the dropwise addition was completed, react at room temperature for 4 h and post-treatment. The reaction solution was extracted with ethyl acetate (80 mL×3), and the organic layers were combined; the organic layer was washed with saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (mobile phase: ethyl acetate-petroleum et...
Embodiment 3
[0032] This embodiment relates to a preparation method of 5-acetoxy-1,4-naphthoquinone (5-acetyljuglone) (III-1) having the structural formula (III), comprising the following steps:
[0033]
[0034] Compound II-1 (3 g, 17.2 mmol) described in Example 1 was dissolved in 10 mL of acetic anhydride, and 5 drops of concentrated sulfuric acid were added dropwise with stirring. The reaction solution was placed in an ice-water bath and stirred for 2 hours. Afterwards, the reaction solution was suction-filtered, washed with ice water and a small amount of methanol successively to obtain about 3.4 g of compound III-1 in the form of light yellow powder crystals, and the yield was 91%. 1 H NMR (400MHz, CDCl 3 ): δ8.05(dd, J=7.9, 1.0Hz, 1H), 7.77(t, J=7.9Hz, 1H), 7.40(dd, J=7.9, 1.0Hz, 1H), 6.95(d, J= 10.3Hz, 1H), 6.85(d, J=10.3Hz, 1H), 2.45(s, 3H, CH 3 CO).
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