Реакция #1106664

ord-af840a28753544d781d0d4fc19ef5f8d

Уравнение реакции

O=C1c2c(O)ccc(O)c2C(=O)c2c(F)c(F)c(F)c(F)c21
1,2,3,4-tetrafluoro-5,8-dihydroxyanthraquinone
CN(C)CCN
N,N-dimethylethylenediamine
CN(C)CCNc1c(F)c(F)c(NCCN(C)C)c2c1C(=O)c1c(O)ccc(O)c1C2=O
Compound 1
CN(C)CCNc1c(F)c(F)c(NCCN(C)C)c2c1C(=O)c1c(O)ccc(O)c1C2=O
1,4-bis(2-(dimethylamino)ethylamino)-2,3-difluoro-5,8-dihydroxyanthracene-9,10-dione

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ДругоеAfter evaporation of the solvents
  2. 2
    Другоеthe residue was purified by silica gel chromatography

Методика

A mixture of 1,2,3,4-tetrafluoro-5,8-dihydroxyanthraquinone (1.0 g, 3.2 mmol) and N,N-dimethylethylenediamine (3 mL) in CH2Cl2 (30 mL) was stirred at room temperature for 12 hours. After evaporation of the solvents, the residue was purified by silica gel chromatography using isocratic solvent system of EtOAc/MeOH/Et3N (10:10:1) yielding 830 mgs of Compound 1 as dark blue product. Abs (max, PBS pH 7.4)=568 nm; Em=675 nm. The structure of Compound 1 is given below:

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08715944B2uspto-grants-2014_05