Benzenamine, 2-bromo-4-nitro- → 3-(2-Bromo-4-nitrophenyl)-1,3-dihydroquinazoline-2,4-dione

HRID 1071746

Reaktionsgleichung

Reaktionsgleichung von HRID 1071746
[N:1]([C:4]1[CH:13]=[CH:12][CH:11]=[CH:10][C:5]=1[C:6]([O:8]C)=O)=[C:2]=[O:3].[Br:14][C:15]1[CH:21]=[C:20]([N+:22]([O-:24])=[O:23])[CH:19]=[CH:18][C:16]=1[NH2:17].CCN(C(C)C)C(C)C.C1CCN2C(=NCCC2)CC1>CN(C=O)C>[Br:14][C:15]1[CH:21]=[C:20]([N+:22]([O-:24])=[O:23])[CH:19]=[CH:18][C:16]=1[N:17]1[C:6](=[O:8])[C:5]2[C:4](=[CH:13][CH:12]=[CH:11][CH:10]=2)[NH:1][C:2]1=[O:3]

Komponenten

6

Edukt 4

HCID 25840Benzenamine, 2-bromo-4-nitro-HCID 811841,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81531DiisopropylethylamineHCID 519494Methyl 2-isocyanatobenzoate

Produkt 1

HCID 220644013-(2-Bromo-4-nitrophenyl)-1,3-dihydroquinazoline-2,4-dioneAusbeute 44,2 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6228DimethylformamideLösungsmittel

Versuchsvorschrift

To a solution of methyl 2-isocyanatobenzoate (0.266 g, 1.5 mmol) and 2-bromo-4-nitroaniline (0.325 g, 1.5 mmol) in DMF (2 mL) was added DIEA (0.79 mL). The reaction mixture was stirred at room temp for 24 hr, with addition of DBU (0.22 mL) at 17 hr. The reaction mixture was extracted with EtOAc, washed with 1 N HCl and brine, dried and concentrated to give crude product, which was chromatographed on silica gel with 10% EtOAc/CH2Cl2 to give 3-(2-bromo-4-nitrophenyl)-1,3-dihydroquinazoline-2,4-dione (0.24 g, 44%). ES-MS (M+H)+=362, 364 (Br).

Aufarbeitung

  1. extractionThe reaction mixture was extracted with EtOAc
  2. washwashed with 1 N HCl and brine
  3. customdried
  4. concentrationconcentrated
  5. customto give crude product, which
  6. customwas chromatographed on silica gel with 10% EtOAc/CH2Cl2

Quellen und Nachweise

ORD-Eintrag
ord-e9b92a9ff470427bb9eb9f9325b7460f
Quelldatensatz
uspto-grants-2005_06
Patentnummer
US06906063B2

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