A practical approach for the preparation of monofunctional azulenyl squaraine dye

摘要

The synthesis of monofunctional azulenyl squaraine dye >NIRQ700 is described. The essential azulene intermediate >3, 1-(methoxycarbonyl)-2-methylazulene, was achieved via [8+2] cycloaddition between lactone >2, 2H-3-methoxycarbonyl-cyclohepta[b]furan-2-one, and the in situ generated vinyl ethers under high temperature and pressure conditions. Methylation on the cycloheptatriene ring of 2-methyl azulene >6 via Meisenheimer-type intermediate following Schrott's method formed the carboxylic acid intermediate >9, 3-(2-methyl-azulen-4-yl)-propionic acid. Condensation of >9 with squaric acid provided the title compound >NIRQ700 at moderate yields. The non-fluorescent squaraine dye >NIRQ700 absorbed in a 600–700 nm range and potentially can be used to quench a number of available NIR fluorochromes in order to extend the spectrum of biological quenching assays.