Asymmetric cyanine dye compound and its application
A technology of cyanine dyes and compounds, applied in the field of application of ROX channel fluorescence quenchers
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Embodiment 1
[0033] Embodiment 1: the synthesis of compound (III)
[0034]
[0035] 2,3-Dimethylbenzoxazole p-toluenesulfonate (180mg, 0.52mmol), benzamidine (160mg, 0.8mmol) and 2ml of acetic anhydride were refluxed for 30 minutes, cooled and dropped into ether to obtain Product 170mg.
[0036] Product NMR data 1 HNMR: 1.82 (s, 3H), 2.34 (s, 3H), 6.06 (m, 1H), 7.7 (m, 1H), 4.39 (s, 3H), 7.5-8.6 (m, 13H).
Embodiment 2
[0037] Embodiment 2: the synthesis of compound (II)
[0038]
[0039] 4-Methylquinoline (4.8ml, 0.0363mol) and methyl 2-(4-(bromomethyl)-2-nitrophenyl)propionate (prepared according to NaokiYamakawa et al., Bioorganic & Medicinal Chemistry 19(2011) 3299-3311) (16.44g, 0.05445mol) mixed, react overnight at 110°C, after cooling, add 20ml of methanol to dissolve, then hang and steam to obtain a viscous solid, then add 200ml of acetone and stir, after stirring for 2h, the product precipitates, filter, and dry to obtain the product Compound (II) 6.4g.
[0040] Product NMR data 1 HNMR: 1.51 (s, 3H), 2.66 (s, 3H), 3.6 (d, 3H), 3.7 (m, 1H), 5.95 (s, 2H), 7.5-8.6 (m, 9H).
Embodiment 3
[0041] Embodiment 3: the synthesis of compound (I-1)
[0042]
[0043] Compound III (58mg, 0.13mmol) and compound (II) (89mg, 0.2mmol) were dissolved in 2ml of pyridine, and heated to reflux for 30 minutes. After the reaction was completed, the pyridine was removed by rotary evaporation, and the residue was poured into water, and 5% Hydrochloric acid, filter after the product is precipitated, dissolve the product obtained by filtration in 30ml of methanol and water (volume ratio 1:1), add 80mg of sodium hydroxide for hydrolysis, after hydrolysis, drop concentrated hydrochloric acid again, after the product precipitates, Filter and dry to get the final product.
[0044] Product NMR data 1HNMR: (1.56(m, 3H), 3.82(m, 1H), 4.39(s, 3H), 5.5(m, 3H), 6.65(m, 1H), 6.71(m, 1H), 8.54(m, 1H ), 7.3-8.6 (m, 12H).
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