A kind of asymmetric cyanine dye compound and application
A technology of cyanine dyes and compounds, which is applied in the application field of 650nm channel fluorescent quencher, which can solve the problems of insufficient quenching efficiency and limitation of signal dynamics characteristics, etc.
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Embodiment 1
[0033] Embodiment 1: the synthesis of compound (III)
[0034]
[0035] 2,3-Dimethylbenzothiazole p-toluenesulfonate (180mg, 0.52mmol), benzamidine (160mg, 0.8mmol) and 2ml of acetic anhydride were refluxed for 30 minutes, and after cooling, they were dropped into diethyl ether to obtain 170mg of the product .
[0036] Product NMR data 1 HNMR: 1.82 (s, 3H), 2.34 (s, 3H), 6.06 (m, 1H), 7.6 (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 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 (60mg0.13mmol) and compound (II) (89mg, 0.2mol) were dissolved in 2ml of pyridine, heated to reflux for 30 minutes, after the reaction was completed, the pyridine was removed by rotary evaporation, the residue was poured into water, and 5% hydrochloric acid was added dropwise , filter after the product is precipitated, dissolve the product obtained by filtration in 30ml of 1:1 methanol and water, add 80mg of sodium hydroxide for hydrolysis, after hydrolysis, drop concentrated hydrochloric acid again, after the product precipitates, filter and dry to obtain the final product.
[0044] Product NMR data 1 HNMR: 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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