Dimethylformamide → 4-Amino-6-benzyloxy-2-chloro-7-methoxyquinazoline

HRID 2228489Notes

Reaction equation

HRID 2228489 reaction equation
CN(C)C=O.P(Cl)(Cl)([Cl:8])=O.[NH2:11][C:12]1[C:21]2[C:16](=[CH:17][C:18]([O:30][CH3:31])=[C:19]([O:22][CH2:23][C:24]3[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=3)[CH:20]=2)[N:15]=[C:14](O)[N:13]=1.C(=O)([O-])[O-].[Na+].[Na+]>C(O)(C)C.C(OCC)(=O)C>[NH2:11][C:12]1[C:21]2[C:16](=[CH:17][C:18]([O:30][CH3:31])=[C:19]([O:22][CH2:23][C:24]3[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=3)[CH:20]=2)[N:15]=[C:14]([Cl:8])[N:13]=1

Participants

7

Reactant 4

HCID 6228DimethylformamideHCID 10340Sodium CarbonateHCID 24813Phosphorus oxychlorideHCID 178486884HCID 178486884, compound

Product 1

HCID 109799944-Amino-6-benzyloxy-2-chloro-7-methoxyquinazolineYield 27%

Reagents, catalysts & solvents 2

HCID 3776IsopropanolSolventHCID 8857Ethyl AcetateSolvent

Conditions

Temperature
90 °C

Procedure

N,N-Dimethyl formamide (7.9 ml, 0.10 mol) was added dropwise to phosphorus oxychloride (47.9 ml, 0.52 mol) with stirring. After 10 minutes, 4-amino-6-benzyloxy-2-hydroxy-7-methoxyquinazoline (16.4 g, 0.055 mol) was added portionwise and the resulting mixture heated at 90° C. for 1.5 hours, then cooled and poured into ethyl acetate (750 ml). The mixture was neutralised by the portionwise addition of aqueous sodium carbonate and the phases were separated. The organic layer was evaporated to dryness and the residue combined with the organic phase which was then treated with aqueous sodium hydroxide to basify (pH10) and the mixture was heated at 90° C. for 2 hours. After cooling, the mixture was partitioned between dichloromethane (11) and water (11), the organic phase washed with water, dried over MgSO4 and evaporated to give a pale yellow solid. Trituration with isopropanol afforded the subtitle compound as a colourless solid (4.64 g, 27%). Rf 0.64 (ethyl acetate:methanol 95:5, v/v). MS m/z 316, 318 (MH+).

Workup

  1. temperaturecooled
  2. customthe phases were separated
  3. customThe organic layer was evaporated to dryness
  4. additionwas then treated with aqueous sodium hydroxide
  5. temperaturethe mixture was heated at 90° C. for 2 hours
  6. temperatureAfter cooling
  7. customthe mixture was partitioned between dichloromethane (11) and water (11)
  8. washthe organic phase washed with water
  9. dry with materialdried over MgSO4
  10. customevaporated
  11. customto give a pale yellow solid

Sources & evidence

ORD record
ord-a1aa1a0575e546f1b29a9aae380ac2ef
Source dataset
uspto-grants-2002_07
Patent number
US06417194B1

Reaction notes

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