Ammonia → 7-Nitroquinazolin-4-amine

HRID 876606

Reaktionsgleichung

Reaktionsgleichung von HRID 876606
Cl[C:2]1[C:11]2[C:6](=[CH:7][C:8]([N+:12]([O-:14])=[O:13])=[CH:9][CH:10]=2)[N:5]=[CH:4][N:3]=1.[NH3:15]>CO>[N+:12]([C:8]1[CH:7]=[C:6]2[C:11]([C:2]([NH2:15])=[N:3][CH:4]=[N:5]2)=[CH:10][CH:9]=1)([O-:14])=[O:13]

Komponenten

4

Versuchsvorschrift

A mixture of 1.6 g of 4-chloro-7-nitroquinazoline in 50 ml 7N ammonia in methanol was stirred overnight at rt and concentrated to dryness. The solid was suspended in water, filtered, rinsed with water followed by ether and dried overnight in vacuum oven to provide 0.98 g of 7-nitroquinazolin-4-amine (compound 98-2).

Aufarbeitung

  1. concentrationconcentrated to dryness
  2. filtrationfiltered
  3. washrinsed with water
  4. customdried overnight in vacuum oven

Quellen und Nachweise

ORD-Eintrag
ord-1bcd3184a8ff4d60b219145e85c3fa70
Quelldatensatz
uspto-grants-2015_03
Patentnummer
US08987242B2

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