Novel gas signal molecule donator and preparation method and use thereof
A compound, C1-C20 technology, applied in the field of medicine, can solve problems such as fatal cardiovascular events, and achieve the effect of good safety and tolerability, and high pharmacological activity
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Embodiment 2
[0059] Example 2: E-2-(4-methoxyphenyl)-3-(4-methanesulfonylphenyl)-acrylic acid 4-(3H-1,2-dithio-hole-3- Synthesis of Thione-5-yl)-Phenyl Ester (YLXYⅡ-1)
[0060] Will 6a (0.203g, 0.61mmol), ADT-OH (0.152g, 0.67mmol) and BOP (0.323g, 0.73mmol) were added to 15mL of dry THF, then triethylamine (0.35mL, 2.44mmol) was added, stirred at room temperature 12h, then add 15mL ethyl acetate to dilute, then use 1 mol.L -1 Hydrochloric acid solution (3×15mL), saturated NaHCO 3 solution (3×15mL) and saturated brine (3×15mL), and the organic phase was washed with anhydrous MgSO 4 Drying, evaporation to dryness, column chromatography [petroleum ether (60-90):ethyl acetate=6:1 (v / v)], a red solid was obtained with a yield of 85.6%, mp: 72.1~73.1°C.
[0061] 1 H NMR (400MHz, CDCl 3 ), δ(ppm): 8.08 (s, 1H, =CH), 8.00(m, 3H, ArH), 7.83 (m, 3H, ArH), 7.42 (m, 3H, ArH & =CH), 7.28 (d , 2H, J = 8.7 Hz, ArH), 7.00 (d, 2H, J = 7.8 Hz, ArH), 3.77 (s, 3H, CH 3 ), 3.22 (s, 3H, CH 3 ).
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Embodiment 3
[0065] Example 3: E-2-(2,4-dichlorophenyl)-3-(4-methylsulfonylphenyl)-acrylic acid 4-(3H-1,2-dithio-hole-3 Synthesis of -thione-5-yl)-phenyl ester (YLXYⅡ-2)
[0066] According to the synthetic method of YLXYⅡ-1, ADT-OH and 6b Preparation, red solid, yield 86.9%, mp: 179.1~180.1℃.
[0067] 1 H NMR (400MHz, CDCl 3 ), δ(ppm): 8.28 (s, 1H, =CH), 8.00 (d, 2H, J = 7.7 Hz, ArH), 7.90(m, 4H, ArH), 7.51 (d, 1H, J = 7.1 Hz, ArH), 7.40 (m, 4H, ArH), 6.87(s, 2H, ArH), 6.65(s, 1H, =CH), 3.22 (s, 3H, CH 3 ).
[0068] IR(KBr, cm -1 ): 1739.8 (C=O), 1490.9, 1521.8, 1637.6, 1595.1 (C=C), 1151.5 (C=S).
[0069] HR-MS: Calcd. For C 25 h 16 Cl 2 o 4 S 4 577.9309, Found: 577.9308.
Embodiment 4
[0070] Example 4: E-2-(2-chlorophenyl)-3-(4-methylsulfonylphenyl)-acrylic acid 4-(3H-1,2-dithio-hole-3-thione -5-yl)-phenyl ester (YLXYⅡ- 3 )Synthesis
[0071] According to the synthetic method of YLXYⅡ-1, ADT-OH and 6c Preparation, red solid, yield 81.5%, mp: 176.4-177.4°C.
[0072] 1 H NMR (400MHz, CDCl 3 ), δ(ppm): 8.25 (s, 1H, =CH), 8.01 (d, 2H, J = 8.7 Hz, ArH), 7.83 (m, 3H, ArH & =CH), 7.67 (d, 1H, J = 8.1 Hz, ArH), 7.50 (m, 1H, ArH), 7.42(m, 4H, ArH), 7.37 (d, 2H, J = 2.0 Hz, ArH), 3.22 (s, 3H, CH 3 ).
[0073] 13 C NMR (400MHz, CDCl 3 ), δ(ppm): 220.887, 177.937, 169.575, 158.848, 147.066, 146.892, 143.851, 141.339, 138.985, 138.507, 136.970, 136.844, 136.227, 136.141, 135.213, 134.522, 134.258, 133.484, 132.519, 128.340, 48.500.
[0074] IR(KBr, cm -1): 1734.0 (C=O), 1654.9, 1635.6, 1598.9, 1489.0 (C=C), 1151.5 (C=S).
[0075] HR-MS: Calcd. For C 25 h 17 ClO 4 S 4 545.9669, Found: 545.9661.
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