Reaktion #42128

ord-c28aed103c1d4bb9b51add5a63dc8396

Reaktionsgleichung

COC(=O)c1c(NC(C)=O)c2cc(-c3ccc(Cl)cc3)c(-c3ccc(Cl)cc3Cl)nc2n(C)c1=O
product
COC(=O)c1c(NC(C)=O)c2cc(-c3ccc(Cl)cc3)c(-c3ccc(Cl)cc3Cl)nc2n(C)c1=O
Methyl 4-(acetylamino)-6(4-chlorophenyl)-7-(2,4-dichlorophenyl)-1-methyl-2-oxo-1,2-dihydro-1,8-naphthyridine-3-carboxylate
CNC.Cl
dimethylamine hydrochloride
[CH3][Al]([CH3])[CH3]
Al(CH3)3
CC(=O)Nc1c(C(=O)N(C)C)c(=O)n(C)c2nc(-c3ccc(Cl)cc3Cl)c(-c3ccc(Cl)cc3)cc12
4-(acetylamino)-6-(4-chlorophenyl)-7-(2,4-dichlorophenyl)-N,N,1-trimethyl-2-oxo-1,2-dihydro-1,8-naphthyridine-3-carboxamide

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.STIRRINGThe reaction stirred for 3.5 hours at 50° C.
  2. 2
    Sonstigewas quenched with aqueous 1 M HCl
  3. 3
    workup.ADDITIONThe reaction was diluted with EtOAc
  4. 4
    Waschenwashed with aqueous 1 M HCl
  5. 5
    TrocknenThe solution was dried (Na2SO4)
  6. 6
    Einengenconcentrated
  7. 7
    SonstigeThe concentrated residue was purified by preparative TLC on silica gel
  8. 8
    Wascheneluted 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.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07728141B2uspto-grants-2010_06