Reaktion #42128
ord-c28aed103c1d4bb9b51add5a63dc8396
Reaktionsgleichung
product
Methyl 4-(acetylamino)-6(4-chlorophenyl)-7-(2,4-dichlorophenyl)-1-methyl-2-oxo-1,2-dihydro-1,8-naphthyridine-3-carboxylate
dimethylamine hydrochloride
Al(CH3)3
→
4-(acetylamino)-6-(4-chlorophenyl)-7-(2,4-dichlorophenyl)-N,N,1-trimethyl-2-oxo-1,2-dihydro-1,8-naphthyridine-3-carboxamide
Edukte
Reagenzien
Keine
Reaktionsbedingungen
Detaillierte Bedingungen
See reaction.notes.procedure_details.
Aufarbeitung
- 1workup.STIRRINGThe reaction stirred for 3.5 hours at 50° C.
- 2Sonstigewas quenched with aqueous 1 M HCl
- 3workup.ADDITIONThe reaction was diluted with EtOAc
- 4Waschenwashed with aqueous 1 M HCl
- 5TrocknenThe solution was dried (Na2SO4)
- 6Einengenconcentrated
- 7SonstigeThe concentrated residue was purified by preparative TLC on silica gel
- 8Wascheneluted with 6% methanol in CH2Cl2 affording the title compound
Vorschrift
To dimethylamine hydrochloride (26.1 mg) in toluene (2 mL) was added Al(CH3)3 (0.16 mL) at 0° C. The reaction stirred for about 30 minutes before adding the product of EXAMPLE 91 (85 mg) in toluene (1 mL). The reaction stirred for 3.5 hours at 50° C. and was quenched with aqueous 1 M HCl. The reaction was diluted with EtOAc washed with aqueous 1 M HCl. The solution was dried (Na2SO4) and concentrated. The concentrated residue was purified by preparative TLC on silica gel eluted with 6% methanol in CH2Cl2 affording the title compound. HPLC/MS: 543.0 (M+1), 545.0 (M+3); Rt=3.51 min.