Reaktion #53329
ord-aec5bb57d76b45cbac751505cdb98cb7
Reaktionsgleichung
chloroacetic acid methyl ester
sodium hydride
compound ( 1 )
4-[[4-amino-6-[(2,6-dichlorophenyl)methyl]-1,3,5-triazin-2-yl]amino]benzonitrile
DMF
→
methyl N-(4-cyanophenyl)-N-[4-amino-6-[(2,6-dichlorophenyl)methyl]-1,3,5-triazin-2-yl]glycine
Ausbeute 19.4%
Edukte
Reagenzien
Keine
Reaktionsbedingungen
Temperatur
70°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.
Aufarbeitung
- 1SonstigeThe reaction mixture was then quenched with water
- 2Filtrationthe resulting solid was filtered off
- 3workup.ADDITIONThe residue was treated with hot ACN
- 4Filtrationfiltered while still hot
- 5SonstigeThe residue from the cooled filtrate was recrystallized from 1,4-dioxane
- 6FiltrationThe precipitate was filtered off
Vorschrift
A solution of sodium hydride (0.00195 mol) in DMF (7 ml) was added to compound (1) (0.00186 mol) and the resulting solution was stirred for 5 minutes under argon. Then, chloroacetic acid methyl ester (0.0186 mol) was added and the reaction mixture was heated to 70° C. for 19 hours. The reaction mixture was then quenched with water and the resulting solid was filtered off. The residue was treated with hot ACN, then filtered while still hot. The residue from the cooled filtrate was recrystallized from 1,4-dioxane. The precipitate was filtered off, yielding 0.16 g (19.4%) of methyl N-(4-cyanophenyl)-N-[4-amino-6-[(2,6-dichlorophenyl)methyl]-1,3,5-triazin-2-yl]glycine (compound 39).