Réaction #1563891
ord-270ea86498a74b5889390c8f103fb76a
Équation de réaction
bis(2-bromoethyl)amine
Compound 25
2-amino-N-(2-methoxyphenyl)-6-(4-nitrophenylthi-o)benzamide
NaOH
→
solid
Rendement 82.0%
N-(2-methoxyphenyl)-2-((4-nitrophenyl)thio)-6-(piperazinyl)benzamide
Rendement 82.0%
Réactifs
Réactifs
Aucun
Solvants
Conditions de réaction
Conditions détaillées
See reaction.notes.procedure_details.
Traitement
- 1Autreto get crude product
- 2FiltrationThe crude solid was filtered
- 3Lavagewashed several times with water
- 4Autrepurified by silica gel column chromatography (1:3 v/v ethyl acetate/petroleum ether)
Mode opératoire
Compound 25 (1.0 equiv.) was dissolved in DMF (40 mL) at room temperature. To this mixture bis(2-bromoethyl)amine (1.0 equiv.) was added, following the addition of NaOH (2.0 equiv.). After being stirred for 2 Hours at room temperature, the reaction mixture was poured into ice-cold water (200 mL) to get crude product. The crude solid was filtered and washed several times with water and purified by silica gel column chromatography (1:3 v/v ethyl acetate/petroleum ether) to provide a yellow solid (380.9 mg, 82% yield).