Phosphorus pentachloride → 2-Methylquinazolin-5-amine

HRID 1444484Notes

Reaction equation

HRID 1444484 reaction equation
[CH3:1][C:2]1[NH:11][C:10](=O)[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][C:8]=2[N+:13]([O-])=O)[N:3]=1.P(Cl)(Cl)(Cl)(Cl)Cl.C([O-])(O)=O.[Na+]>P(Cl)(Cl)(Cl)=O.[Pd]>[NH2:13][C:8]1[CH:7]=[CH:6][CH:5]=[C:4]2[C:9]=1[CH:10]=[N:11][C:2]([CH3:1])=[N:3]2

Participants

6

Procedure

12.7 g (62 mmol) of 2-methyl-5-nitro-3H-quinazolin-4-one (M. T. Bogert, V. J. Chambers J. Org Chem. 1905, 649-658) and 37.5 g of phosphorus pentachloride are refluxed in 75 ml of phosphoryl chloride over 20 hours. After cooling, it is poured into saturated NaHCO3 solution and extracted with ethyl acetate. The organic phase is dried, and the solvent is removed. 14 g of 4-chloro-2-methyl-5-nitroquinazoline, of which 4.5 g (20.2 mmol) in 225 ml of ethyl acetate and 22.5 ml of triethylamine are dissolved, is obtained. 2 g of palladium is added to carbon, and it is stirred while being cooled with ice for 4 hours under hydrogen atmosphere at normal pressure. Catalyst is removed from the solution by means of filtration through Celite, whereby it is rewashed with 200 ml of ethanol and concentrated by evaporation. After chromatography on silica gel with ethyl acetate-ethanol (0-10%), 530 mg of the product is obtained.

Workup

  1. temperatureAfter cooling
  2. extractionextracted with ethyl acetate
  3. customThe organic phase is dried
  4. customthe solvent is removed
  5. dissolution14 g of 4-chloro-2-methyl-5-nitroquinazoline, of which 4.5 g (20.2 mmol) in 225 ml of ethyl acetate and 22.5 ml of triethylamine are dissolved
  6. customis obtained
  7. temperaturewhile being cooled with ice for 4 hours under hydrogen atmosphere at normal pressure
  8. customCatalyst is removed from the solution by means of filtration through Celite, whereby it
  9. concentrationconcentrated by evaporation

Sources & evidence

ORD record
ord-2b0f28c949b74bfa8e7392aa6d9498fa
Source dataset
uspto-grants-2010_02
Patent number
US07662821B2

Reaction notes

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