Dimethylformamide → 4-Chloro-6-methoxy-7-(2-methoxyethoxy)quinazoline

HRID 1596267Notes

Reaction equation

HRID 1596267 reaction equation
CN(C=O)C.[CH3:6][O:7][C:8]1[CH:9]=[C:10]2[C:15](=[CH:16][C:17]=1[O:18][CH2:19][CH2:20][O:21][CH3:22])[N:14]=[CH:13][NH:12][C:11]2=O.S(Cl)([Cl:26])=O>>[Cl:26][C:11]1[C:10]2[C:15](=[CH:16][C:17]([O:18][CH2:19][CH2:20][O:21][CH3:22])=[C:8]([O:7][CH3:6])[CH:9]=2)[N:14]=[CH:13][N:12]=1

Participants

4

Reactant 3

HCID 6228DimethylformamideHCID 24386Thionyl ChlorideHCID 135407708HCID 135407708, compound

Product 1

HCID 107306534-Chloro-6-methoxy-7-(2-methoxyethoxy)quinazolineYield 51%

Procedure

DMF (0.5 ml) was added to a mixture of 6-methoxy-7-(2-methoxyethoxy)-3,4-dihydroquinazolin4-one (5.1 g, 20 mmol) in thionyl chloride (50 ml). The mixture was stirred and heated at reflux for 3 hours, allowed to cool and the excess thionyl chloride removed by evaporation. The residue was suspended in methylene chloride and washed with aqueous sodium hydrogen carbonate solution. The aqueous phase was extracted with methylene chloride and the combined extracts dried (MgSO4). The crude product was recrystallised from methylene chloride/hexane to give 4-chloro-6-methoxy-7-(2-methoxyethoxy)quinazoline (2.8 g, 51% ) as a fine white solid.

Workup

  1. temperatureheated
  2. temperatureat reflux for 3 hours
  3. temperatureto cool
  4. customthe excess thionyl chloride removed by evaporation
  5. washwashed with aqueous sodium hydrogen carbonate solution
  6. extractionThe aqueous phase was extracted with methylene chloride
  7. dry with materialthe combined extracts dried (MgSO4)
  8. customThe crude product was recrystallised from methylene chloride/hexane

Sources & evidence

ORD record
ord-d46fc7681a1b437fae0e61a3674fa7a5
Source dataset
uspto-grants-2001_09
Patent number
US06291455B1

Reaction notes

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