Reaktion #1106671

ord-ad501799f6d14ba1a63371006a21a86c

Reaktionsgleichung

CN(C)CCNc1cccc2c1C(=O)c1cccc(Cl)c1C2=O
Compound 17
CN(C)CCNc1cccc2c1C(=O)c1cccc(Cl)c1C2=O
1-Chloro-5-(2-(dimethylamino)ethylamino)anthracene-9,10-dione
CNCCN(C)C
N,N,N′-trimethylethylenediamine
CN(C)CCNc1cccc2c1C(=O)c1cccc(N(C)CCN(C)C)c1C2=O
solid
Ausbeute 43.4%
CN(C)CCNc1cccc2c1C(=O)c1cccc(N(C)CCN(C)C)c1C2=O
1-((2-(dimethylamino)ethyl) (methyl)amino)-5-(2-(dimethylamino) ethylamino)anthracene-9,10-dione
Ausbeute 43.4%

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Vorschrift

This procedure was carried out as described previously in Example 19, using Compound 17 (500 mg, 1.52 mmol) and N,N,N′-trimethylethylenediamine (988 μL, 7.6 mmol). The dye was obtained as a red solid (260 mg) after Biotage purification using a gradient of methanol in chloroform. Abs (max, PBS pH 7.4)=530 nm; Em=646 nm. The structure of Compound 41 is given below:

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08715944B2uspto-grants-2014_05