HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,5-Dichloroanthraquinone → 1,5-Bis((2-(dimethylamino)ethyl)(methyl)amino)anthracene-9,10-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,5-Dichloroanthraquinone | HCID 6711 | — |
| Reactant | 1,2-Ethanediamine, N1,N1,N2-trimethyl- | HCID 67338 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1,5-Bis((2-(dimethylamino)ethyl)(methyl)amino)anthracene-9,10-dione | HCID 59229118 | — |
Reaction Steps
A mixture of 1,5-dichloroanthraquinone (5.5 g, 20 mmol) and N,N,N′-trimethylethylenediamine (40 ml) was refluxed for 18 h. The mixture was cooled to room temperature, diluted with water (400 mL) and extracted with chloroform (2×200 mL). The combined organic layer was washed with water, brine, dried over MgSO4 and evaporated to dryness. The residue thus obtained was purified by silica gel flash chromatography [CHCl3/MeOH/Et3N (44:5:1)] to provide Compound 9. Abs (max, PBS pH 7.4)=508 nm. The structure of Compound 9 is given below:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08715944B2 |
| Source dataset | uspto-grants-2014_05 |
| ORD ID | ord-ac9cf472fe20486fb5e73b1f3619b2a4 |
| Source note | uspto-grants-2014_05 |