反応 #1106664

ord-af840a28753544d781d0d4fc19ef5f8d

反応方程式

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

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他After evaporation of the solvents
  2. 2
    その他the residue was purified by silica gel chromatography

実験手順

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:

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US08715944B2uspto-grants-2014_05